MAN LC FLD 3x00 Operation Sep13 DOC4820 7850 1 3
MAN LC FLD 3x00 Operation Sep13 DOC4820 7850 1 3
Operating Instructions
(Original Operating Instructions)
Revision: 1.3
Date: September 2013
Operating Instructions
UltiMate 3000 Series:
Fluorescence Detectors FLD-3100 and FLD-3400RS
Declaration of Conformity
( O r i g i n a l D e c l a r a t i o n o f C o n f o r m i t y)
Dionex Softron GmbH herewith declares conformity of the above products with
the respective requirements of the following regulations:
• Low-Voltage Directive 2006/95/EC
• EMC Directive 2004/108/EC
The electrical safety of the products was evaluated based on the following
standard:
• DIN EN 61010-1:2010
Safety requirements for electrical equipment for measurement, control
and laboratory use, Part 1: General Requirements
September 2, 2013
Table of Contents
1 Introduction................................................................................................................... 1
1.1 How to Use This Manual ........................................................................................... 1
1.2 Safety ......................................................................................................................... 3
1.2.1 Symbols on the Instrument and in the Manual ................................................. 3
1.2.2 Safety Precautions ............................................................................................ 5
1.2.3 Consignes de Sécurité....................................................................................... 8
1.3 Intended Use ............................................................................................................ 12
1.4 Federal Communications Commission (FCC) Note ................................................ 14
2 Overview ...................................................................................................................... 15
2.1 Unit Description ....................................................................................................... 15
2.2 Operating Principle .................................................................................................. 16
2.3 Configurations ......................................................................................................... 19
2.4 Interior Components ................................................................................................ 20
2.5 Front Panel Elements ............................................................................................... 21
2.6 Rear Panel ................................................................................................................ 22
2.6.1 Power Switch .................................................................................................. 22
2.6.2 Fuse Cartridge ................................................................................................ 22
2.6.3 USB Port ......................................................................................................... 23
2.6.4 Analog Outputs (Optional) ............................................................................. 23
2.7 Fluid Connections .................................................................................................... 23
2.8 Flow Cells ................................................................................................................ 24
2.9 Lamp ........................................................................................................................ 25
2.10 Leak Sensor.......................................................................................................... 25
2.11 Detector Control .................................................................................................. 26
2.12 System Wellness, Predictive Performance, and Diagnostics ............................... 27
3 Installation ................................................................................................................... 29
3.1 Facility Requirements .............................................................................................. 29
3.2 Unpacking ................................................................................................................ 30
3.3 Positioning the Detector in the UltiMate 3000 System ........................................... 31
3.4 Connecting the Detector .......................................................................................... 32
3.4.1 General Information ....................................................................................... 32
3.4.2 Connecting the USB Cable ............................................................................. 32
3.4.3 Connecting the Power Cord ............................................................................ 34
3.4.4 Connecting the Analog Outputs (Optional) .................................................... 34
3.5 Setting Up the Detector in Chromeleon ................................................................... 37
3.5.1 Loading the USB Driver for the Detector ...................................................... 37
3.5.2 Installing the Detector .................................................................................... 39
3.5.3 Configuring the Detector ................................................................................ 40
3.6 Setting Up the Detector in DCMSLink.................................................................... 44
6 Troubleshooting .......................................................................................................... 97
6.1 Overview .................................................................................................................. 97
6.2 Messages on the Detector Display ........................................................................... 98
6.3 Operating Problems ............................................................................................... 102
11 Index........................................................................................................................... 125
1 Introduction
1.1 How to Use This Manual
The layout of this manual is designed to provide quick reference to the sections of interest
to the reader. However, in order to obtain a full understanding of your Thermo Scientific™
Dionex™ detector, Thermo Fisher Scientific recommends that you review the manual
thoroughly before beginning operation.
All descriptions in the manual apply to the following variants of the fluorescence detector in
the UltiMate™ 3000 series:
• FLD-3100
• FLD-3400RS
This manual is provided "as is". Every effort has been made to supply complete and
accurate information and all technical specifications have been developed with the utmost
care. The information contained in this manual should not be construed as a commitment
by Thermo Fisher Scientific. Thermo Fisher Scientific assumes no responsibility for any
errors that may appear in this document. This document is believed to be complete and
accurate at the time of publication. In no event shall Thermo Fisher Scientific be liable for
incidental or consequential damages in connection with or arising from the use of this
document.
All rights reserved, including those for photomechanical reproduction and storage on
electronic media. No part of this publication may be copied or distributed, transmitted,
transcribed, stored in a retrieval system, or transmitted into any human or computer language,
in any form or by any means, electronic, mechanical, magnetic, manual, or otherwise, or
disclosed to third parties without the express written permission of Thermo Fisher Scientific
Inc.
Trademarks
Analyst is a registered trademark of AB Sciex.
Compass and Hystar are trademarks of Bruker Daltonics.
Empower is a registered trademark of Waters Corp.
PEEK is a trademark of Victrex PLC.
LiChrosolv is a registered trademark of Merck KGAA.
Windows and Windows Vista are registered trademarks of Microsoft Corp.
All other trademarks are property of Thermo Fisher Scientific Inc. and its subsidiaries.
1.2 Safety
The CE Mark label and cTUVus Mark safety label on the instrument indicate that the
detector is compliant with the related standards.
Symbol Description
˜
Alternating current—Courant alternatif
Power supply is on (-)—L'instrument est mis sous tension (-) and Power
supply is off (O)—L'instrument est mis hors tension (O)
Refer to the Operating Instructions to prevent risk of harm to the operator and
to protect the instrument against damage.
Référez-vous à ce manuel pour éviter tout risque de blessure à l'opérateur et/ou
protéger l'instrument contre tout dommage
At various points throughout the manual, messages of particular importance are indicated
by certain symbols:
Important: Indique que ne pas tenir compte de l'information jointe peut conduire
à de faux résultat ou endommager l'instrument.
Avertissement: Indique que ne pas tenir compte de l'information jointe peut entraîner
des blessures corporelles.
When working with analytical instrumentation, you must know the potential hazards of
using chemical solvents.
Tip: Before initial operation of the detector, make yourself familiar with
the contents of this manual.
For the safety precautions in French, see page 8.
Warning: All users of the device must observe the following safety precautions
and all additional safety precautions in this manual to avoid the
possibility of personal injury or damage to the device when
operating the device or carrying out any maintenance or service
procedures.
Observe any warning labels on the device and see the related
sections in these Operating Instructions.
• Protective equipment
When performing any work on or near the HPLC system, wear personal protective
equipment (protective clothing, safety gloves, safety glasses) as required by the hazard of
the mobile phase and sample. For information about the proper handling of a particular
substance and for advice on specific hazards, refer to the material safety data sheet for the
substance you are using. Observe the guidelines of Good Laboratory Practice (GLP).
An eyewash facility and a sink should be close to the device. If any substance splashes on
the eyes or skin, wash the affected area and seek medical attention.
• Hazardous substances
Many organic solvents, mobile phases, and samples are harmful to health. Be sure that
you know the toxic and infectious properties of all substances that you are using. You
may not know the toxic or infectious properties of many substances that you are using. If
you have any doubt about a substance, treat it as if it contains a potentially harmful
substance. For advice on the proper handling of a particular substance, refer to the Safety
Data Sheet (SDS) of the manufacturer. Observe the guidelines of Good Laboratory
Practice (GLP).
Dispose of waste substance in an environmentally safe manner that is consistent with all
local regulations. Do not allow flammable, toxic, and/or infectious substances to
accumulate. Follow a regulated, approved waste disposal program. Never dispose of
flammable, toxic, and/or infectious substances through the municipal sewage system.
• Hazardous gases
Install the HPLC system in a well-ventilated laboratory. If the mobile phase or sample
includes volatile or flammable solvents, do not allow them to enter the workspace. If the
mobile phase or sample includes volatile or flammable solvents, avoid open flames and
sparks.
• Electrostatic discharge
Discharge of electrostatic energy may lead to sparking and can constitute a fire hazard.
Keep in mind that liquid flowing through capillaries can generate static electricity. This
effect is particularly pronounced in insulating capillaries and with non-conductive
solvents (for example, pure acetonitrile).
Take appropriate measures to prevent the generation of static electricity near the HPLC
system. For example, make sure that the air humidity level in the laboratory is
sufficiently high and provide proper ventilation, wear anti-static clothing or shoes,
prevent accumulation of air bubbles in waste lines, and use grounded waste containers.
Use only non-conductive capillaries to direct solvents into the waste container. With
electrically conductive capillaries, make sure that they are properly grounded.
• Self-ignition of solvents
Do not use solvents for which the self-ignition temperature is below 150 °C. In case of
leakage, these solvents may self-ignite on a hot surface.
• Hot surfaces
♦ During operation, the lamps and the surrounding parts become extremely hot and
remain so for some time after the detector is turned off. To avoid possible injury,
allow sufficient time for the lamp to cool down after turning off the detector. Only
then start with the maintenance and repair work.
♦ Flow cells can become extremely hot during operation. To avoid possible injury,
allow sufficient time for the flow cell to cool down before replacing the cell.
• Disconnect the detector from all power sources before removing the panels. When the
panels are removed, dangerous electrical connections will be exposed. The enclosure
must be opened only by Thermo Fisher Scientific service personnel.
• Always replace blown fuses with original spare part fuses authorized by Thermo Fisher
Scientific.
• Replace faulty communication cables.
• Replace faulty power cords. Never use a power cord other than the power cords provided
for the device.
• Use only the original spare parts and accessories authorized for the device by Thermo
Fisher Scientific.
• When lifting or moving the detector, always lift the unit by the bottom sides or sides. Do
not lift the detector by the front panel door. This may damage the door.
• Do not place any heavy objects on the open front panel door. This may damage the door.
• After operation, rinse out buffers and solutions that form peroxides.
• Before switching from buffer to organic solution, rinse the analytical system thoroughly
with deionized or HPLC grade water.
• When switching to another solvent, ensure that the new solvent is miscible with the one
contained in the HPLC system. If the solvents are not miscible, the system can be
damaged, for example, by flocculation.
• If a leak occurs, turn off the instrument and remedy the situation immediately.
• Use only standard solvents (HPLC grade or fluorescence grade for highest sensitivity)
and buffers that are compatible with all parts that may be exposed to solvents.
• Before interrupting operation for several days or more or when preparing the detector for
transport, observe the precautions for shutting down the detector (→ page 93).
• Do not use the detector in ways other than those described in these Operating
Instructions.
• Keep the operating instructions near the device to be available for quick reference.
Si vous utilisez d'instrumentation analytique, vous devez connaître les risques d'utilisation
de produit chimiques.
• Equipment de protection
Pour tous les travaux sur le système HPLC ou à proximité, portez l'équipement de
protection personnel (vêtements de protection, gant de sécurité, lunettes de protection)
qui correspond aux risque découlant de la phase mobile et/ou de l'échantillon. Pour les
informations sur la manipulation correcte des composés et des recommandations pour les
situations de risque spécifiques, veuillez consulter la fiche de données de sécurité des
substances que vous utilisez. Veuillez respecter des directives des Bonnes Pratiques de
Laboratoire (BPL).
Une installation permettant de se laver les yeux ainsi qu'un lavabo doivent se trouver à
proximité du système. Si une substance, quelle qu'elle soit, entre en contact avec vos
yeux ou votre peau, rincez abondamment la zone affectée à l’eau, puis.
• Substances dangereuses
De nombreux solvants organiques, phases mobiles et échantillons sont nuisibles à la
santé. Informez-vous de propriétés toxicologiques et infectieuses de toutes les substances
que vous utilisez. Les propriétés toxicologiques et infectieuses de nombreuses substances
peuvent être mal connues. Au moindre doute concernant une substance, traitez-la comme
s'il contenait une substance potentiellement dangereuse. Pour des instructions comment
utiliser correctement des composés particuliers, veuillez consulter à la fiche de données
des sécurités du fabricant respectif. Veuillez respecter des directives des Bonnes
Pratiques de Laboratoire (BPL).
Débarrassez-vous de tous les déchets de substances de manière écologique,
conformément à la règlementation en vigueur au niveau local. Empêchez impérativement
l'accumulation de solvants inflammables, toxiques et/ou infectieux. Suivez un
programme d'élimination des déchets règlementé et approuvé. Ne jetez jamais de
solvants inflammables, toxiques et/ou infectieux dans le système municipal d'évacuation
des eaux usées.
• Gaz dangereux
Installez le système HPLC dans un laboratoire bien ventilé. Si la phase mobile ou
l’échantillon contient des solvants volatils ou inflammables, vous devez assurer qu'ils ne
pénètrent dans l'espace de travail. Si la phase mobile ou l’échantillon contient des
solvants volatils ou inflammables, évitez les flammes nues et les sources d’étincelles à
proximité.
• Décharge électrostatique
Décharge électrostatique peut provoquer la formation d'étincelles et peut présenter un
risque d’incendie. Veuillez noter que des solvants fluides dans les capillaires peuvent se
charger automatiquement. Cet effet se peut produire particulièrement forte dans les
capillaires isolants et avec des solvants non-conducteurs (par exemple, l'acetonitrile pur).
Prenez des mesures appropriées pour éviter les charges électrostatiques à proximité du
système HPLC. Par exemple, s'assurez qu'il y a une humidité de l'air suffisante et une
ventilation adéquate dans la laboratoire, portez des vêtements ou équipement de
protection antistatique, évitez l'accumulation de bulles d'air dans les lignes de déchets et
utilisez des réservoirs à déchets mis à la terre.
Utilisez uniquement des capillaires non-conducteurs pour diriger solvants au réservoir de
déchets. Capillaires électriquement conducteur devrait être mis à la terre.
♦ Dans un système UltiMate 3000 Bio RS, certains capillaires du système Viper sont
faits d'alliage de nickel-cobalt MP35N. Contact avec la peau peut provoquer une
réaction chez les personnes qui sont sensibles au nickel/cobalt.
♦ Portez des lunettes de protection lorsque vous manipulez des capillaires en silice
fondue (pendant l'installation, découpe, etc.).
• Surface chaude
♦ Lampes et les parties environnantes deviennent très chaudes pendant le
fonctionnement. Pour éviter toute blessure, vous attendez après mise hors tension
jusqu'à ce que les lampes soient refroidies. Commencer seulement alors les travaux
d'entretien.
♦ Les cellules de mesure peuvent devenir très chaudes pendant le fonctionnement. Pour
éviter toute blessure, vous attendez jusqu'à ce que la cellule est refroidi avant de
remplacer le capteur.
• Quand les capots de protection de l’appareil sont démontés, vous êtes exposés à des
connexions électriques sous haute tension deviennent accessibles. Débranchez
l'instrument de toute source d'alimentation électrique avant de retirer les capots. Ne
démontez les capots de protection que si cela est explicitement demandé au cours de ces
instructions. Les capots de protection devraient être démontés uniquement par le
personnel de service de Thermo Fisher Scientific.
• Remplacez toujours les fusibles grillés par des fusibles de rechange autorisés par Thermo
Fisher Scientific (→ page 114).
• Remplacez les câbles de communication défectueux.
• Remplacez les cordons d'alimentation électrique défectueux. Utilisez uniquement les
cordons d’alimentation électrique spécifique à l’instrument.
• Utilisez seulement des pièces de rechange originales et des accessoires autorisés par
Thermo Fisher Scientific.
• Réglez toujours une limite de pression minimum pour le système HPLC. Ceci prévient
les dommages résultant de fuites ou du fonctionnement à sec de la pompe.
• Lorsque vous soulevez ou l’instrument, tenez-le toujours par le dessous ou par les côtés
de l'unité. Soulever l’instrument par la partie avant inférieure ou par le panneau avant
peut endommager la porte.
• Ne placez aucun objet lourd sur la porte ouverte du panneau avant. Ceci pourrait
endommager la porte.
• Après utilisation, purgez le système des tampons et des susceptibles de former des
peroxydes.
• Lorsque vous passez d’une solution saline à un solvant organique, effectuez un rinçage
intermédiaire du système HPLC à l'eau dé-ionisée ou qualité HPLC.
• Lorsque vous passez à un autre solvant, assurez-vous que le nouveau solvant soit
miscible avec celui qui se trouve dans le système HPLC. Dans le cas contraire, le
système HPLC peut être endommagé; par exemple, par des floculations!
• Si une fuite se produit, arrêtez immédiatement l’instrument, stoppez le débit de la pompe
et remédiez au problème.
• Utilisez uniquement des solvants de qualité HPLC ou qualité fluorescence (pour
maximiser la sensibilité) et des solutions salines compatibles avec les matériaux exposés
phase mobiles.
• Avant d'interrompre le fonctionnement pendant plusieurs jours ou plus, observez les
précautions figurant en page 114).
• De nombreux solvants organiques et solutions salines sont toxiques. Informez-vous des
propriétés toxicologiques de toutes les phases mobiles que vous utilisez.
• N'utilisez pas l'instrument de manière autre que celles décrites dans ce manuel.
• Conservez ce manuel á proximité de l’instrument pour pouvoir le consulter facilement.
For more information, contact the Thermo Fisher Scientific sales organization for Dionex
HPLC Products.
If there is any question regarding appropriate usage, contact Thermo Fisher Scientific before
proceeding.
Avertissement: Si l'instrument est utilisé de façon non spécifiée par Thermo Fisher
Scientific, la protection prévue par l'instrument pourrait être altérée.
Thermo Fisher Scientific n'assume aucune responsabilité et ne sera
pas responsable des blessures de l'operateur et/ou des dommages de
l'instrument. Si la protection de l'instrument n'est pas garanti à tout
moment, débranchez l'instrument de toutes les sources d'alimentation
électrique et assurez-vous que l'instrument n'est pas utilisé
involontairement.
2 Overview
2.1 Unit Description
The detector is a high-quality instrument designed for HPLC analysis as part of the
UltiMate 3000 system.
• A xenon flash lamp is used to exite a wavelength range of 200 to 880 nm.
• With the unique Dual-PMT option, the wavelength range can be extended to the near
infrared spectral region (up to 900 nm) without any loss in sensitivity in the UV/VIS
spectral region.
• Data collection rates in single channel mode of up to 100 Hz (FLD-3100) or up to 200 Hz
(FLD-3400RS under Chromeleon 7) allow rapid separations in UHPLC. The wavelength
switching time is < 250 ms.
• The detector is optimized for high sensitivity (signal-to-noise ratio higher than 550 for
the Raman spectrum of water), over the entire lifetime of the lamp. It is thus possible to
detect even smallest peaks.
• The flow cells are equipped with an active temperature control to ensure improved
reproducibility when ambient temperatures fluctuate.
• To suppress the higher-order radiation typical of grating spectrometers and scattering of
light, the detector is equipped with an optical filter. Users can select the wavelength range
that is suppressed by the filter for FLD-3400RS detectors.
• The FLD-3400RS can measure up to four channels (2D data) with independent
parameters (wavelengths, sensitivity, filter wheel) simultaneously.
• The detector can be controlled by the Chromeleon Chromatography Management
System. This provides a high degree of system integration, as well as maximum analysis
efficiency due to comprehensive data analysis and evaluation features in Chromeleon.
• Various safety and monitoring features are provided for optimum system performance
and reliability (→ page 27).
• All parts that may be exposed to solvents are made of materials that provide optimum
resistance to the most commonly used solvents and buffer solutions in HPLC.
Emission of
light of a longer
wavelength
As shown in Fig. 3 (→ page 17), the light beam from the xenon lamp (no. 1) is focused by the
lamp optics (no. 2) through the entrance of the excitation monochromator (no. 3). The
excitation monochromator transmits only light of the user-selected wavelength to the sample
inside the flow cell (no. 4). Most of the light penetrates the sample. A reference detector
(no. 5) behind the flow cell measures the intensity of this light. The excitation light stimulates
the sample to emit fluorescence light.
When the light exits the flow cell, it is focused by the emission optics (no. 6) through the
emission monochromator (no. 8).
A cut-off filter, which lets only light above a certain wavelength pass, is located before the
emission monochromator. In the FLD-3100, the filter has a fixed cut-off wavelength
(280 nm). In the FLD-3400RS, a filter wheel (no. 7) is installed. With the help of a motor the
wheel can be moved to 5 different positions with different cut-off wavelengths. The selectable
filter helps to achieve an even better sensitivity and increase flexibility during method
development.
The emission monochromator transmits only the light with the user-selected emission
wavelength to a photomultiplier tube (PMT) (no. 9), where the light is measured. A second
optional red-sensitive photomultiplier tube (no. 10) measures light in the near infrared region
(up to 900 nm).
2.3 Configurations
The detector is available in the following configurations:
Dual-PMT
The variants of the FLD with Dual PMT are equipped with a second PMT for the near
infrared region (up to 900 nm) (→ no. 10, Fig. 3, page 17). Depending on the PMT setting,
the instrument selects the suitable PMT for each measurement, or you can manually select
which PMT should be used. For emission scans, you can scan with both PMTs
simultaneously.
Detectors with a single PMT can later be upgraded with a second PMT by the Thermo
Fisher Scientific Service for Dionex HPLC Products.
Important: The open front panel door is not designed to carry weight. Therefore,
you should not place any objects on the open front panel door.
Important: Ne placez aucun objet lourd sur la porte ouverte du panneau avant.
Ceci pourrait endommager la porte.
1
1
2 3
No. Description
1 Slots in the enclosure to route the flow cell capillaries to the outside (→ page 23)
Two more slots with capillary guides are provided in the enclosure bottom.
2 Leak sensor (→ page 25)
3 Flow cell
No flow cell is installed when the detector is shipped. Before initial operation, install a flow cell.
1
2
1 2 3 4 5 6
Fig. 6: Rear panel
No. Description
The power switch on the rear panel is the main power switch for the detector. Turn on the
power switch before initial operation of the detector and leave it on. For routine operation,
leave the main power switch on. For routine on/off control, use the standby button on the
front of the detector (→ page 21). Press and hold the button for about one second to allow
the detector to change the mode. Turn off the main power switch when instructed to do so,
for example, before performing a service procedure or when interrupting operation for
longer periods (one week or more). Observe the precautions on page 93.
The fuse cartridge contains two slow-blow fuses, rated at 2 A (5 x 20 mm). For
information about how to change the fuses, see page 114.
If the optional DAC plug-in module (part no. 6078.0305) is installed, two analog outputs
with a resolution of 20 bits each are provided. The outputs can be connected to additional
evaluation devices. The analog output voltages are updated with the data rate selected in
Chromeleon (Data Collection Rate), however, not exceeding a maximum data rate of
50 Hz. For information about how to install the board, see page 34. For configuration
details, see page 36.
When closing the front panel door, avoid bending the capillaries and make sure that they are
routed to the outside through these slots.
Tip: The volume between the column and the flow cell should be as low as possible
to avoid peak broadening effects and the accompanying loss of
chromatographic efficiency. Preferably use Viper capillaries to prevent dead
volume.
Volume
Flow cell
Flow cell type Flow cell volume Heat exchanger Part no.
material
and/or inlet capillary
All parts of the flow cell that are exposed to solvents are made of fused silica, stainless
steel, or PTFE (Polytetrafluorethylene).
All flow cells are optimized for fast separations with no loss in chromatographic
resolution. An identification chip is fitted to the flow cell in the factory. The chip stores
unique information about the flow cell, including the cell type and serial number. When the
flow cell is installed, a contact on the flow cell connects the chip to the detector
electronics.
The flow cells are equipped with a temperature control. Flow cell and heat exchanger can be
heated to a user-defined temperature (→ page 88). The heat exchanger helps to adapt the
temperature of the mobile phase to the flow cell temperature before the mobile phase enters
the optical part of the cell. Note that the volume of the heat exchanger and inlet capillary
indicated in the table influences the retention times and peak widths.
The micro flow cell is optimized for best resolution in UHPLC, and is recommended for use
with 2.1 mm ID columns. The analytical flow cell provides higher sensitivity and a better
signal-to-noise ratio with most other columns.
To ensure optimum performance of the flow cells, observe the guidelines (→ page 53).
2.9 Lamp
The light source is a xenon flash lamp with a power of 15W. The flash frequency of the
lamp varies, depending on the selected lamp mode.
The lamp is turned on when data acquisition starts, and automatically turned off after data
acquisition was stopped to extend its lifetime. It is not required that the lamp is turned on
during the entire chromatographic separation. For example; during re-equilibration of the
chromatographic column, usually no peaks of interest will elute. If you are not interested in
the baseline during the wash and re-equilibration phase, you can turn off the lamp by stopping
data acquisition, or set the lamp mode to a lower frequency. This will save lamp power on
time or reduce the number of lamp flashes, respectively, and thus extend the lamp lifetime. In
addition, you can extend the lamp lifetime by selecting a different lamp mode (→ page 88).
The lamp must be replaced only by Thermo Fisher Scientific Service for Dionex HPLC
Products.
When the leak sensor reports a leak, eliminate the cause for the leakage and dry the leak
sensor (→ page 113). If the sensor is not dry, the Status LED remains red. To remove the
message from the display, select Clear on the navigation bar.
Tip: All software details in this manual refer to Chromeleon 6.80, unless stated
otherwise.
If you want to operate the detector with Chromeleon 7, refer to the following
documents for information about how to perform the related processes in
Chromeleon 7 (all documents are included in the Chromeleon 7 shipment):
• Chromeleon 7 Help—provides extensive information and comprehensive
reference material for all aspects of the software.
• Quick Start Guide—describes the main elements of the user interface and
guides you step-by-step through the most important workflows.
• Reference Card—provides a concise overview of the most important
workflows.
• Installation Guide—provides basic information about module installation
and configuration. For specific information about a certain module, refer
to the Chromeleon 7 Instrument Configuration Manager Help.
Note the following:
• Chromeleon 7 terminology is different from the terminology used in
Chromeleon 6.80. For details, refer to the Glossary, which is available in
the Documents folder of your Chromeleon 7 installation.
• Chromeleon 7 may not yet support all functions supported in
Chromeleon 6.80.
• Direct Control
With direct control, you select operating parameters and commands in the Commands
(F8) dialog box. Direct commands are executed as soon as they are entered. For routine
operation, most parameters and commands are available also on a control panel. For
more information about direct control, see page 65.
• Automated Control
With automated control, you create a program (or PGM File). This is a list of control
commands, executed in chronological order, for automated operation of the detector.
Programs can be created automatically with the help of a software wizard or manually by
editing an existing program. For more information about automatic control, see page 67.
When an error is detected, the Status LED on the front panel is red and a message appears on
the detector display (→ page 98).
3 Installation
3.1 Facility Requirements
The installation site must meet the following requirements:
• The main power switch and the main power receptacle are on the rear panel. Make sure
that
♦ Free and unrestricted access to the main power switch is ensured at all times.
♦ The power cord of the device can be easily reached and disconnected from the power
line at all times. Provide sufficient space behind the device to unplug the cable.
• Make sure that the installation site meets the power and environmental specifications
listed in the Technical Information section (→ page 117).
• Install the detector in the laboratory on a stable surface that is free of vibrations.
• Make sure that the surface is resistant to solvents.
• Avoid locations with extreme changes in temperature.
• Avoid direct sunlight and high humidity.
• Allow sufficient clearance behind and to the sides of the detector for ventilation.
3.2 Unpacking
All electrical and mechanical components of the detector are carefully tested before the
instrument is shipped from the factory. After unpacking the detector, inspect the module
for any signs of mechanical damage, which might have occurred during transit.
Tips: Immediately report any shipping damage to both, the incoming carrier and
Thermo Fisher Scientific. Shipping insurance will compensate for the damage
only if reported immediately.
Keep the original shipping container and packing material. They provide
excellent protection for the instrument in case of future transit. Shipping the
unit in any other packaging automatically voids the product warranty.
1. Place the shipping container on the floor and remove the accessories kit and the power
cord.
2. Grasp the detector by the sides. Slowly and carefully, pull the instrument out of the
shipping container and place it on a stable surface.
Important: To prevent the device from falling, grasp the device by the
sides, and then lift the unit together with the foam spacers out
of the shipping container. Do not lift the unit by the
packaging material or the front panel.
Fig. 7: Module arrangement for an UltiMate 3000 RS system with two detectors (example)
Left from top to bottom: SR-3000 solvent rack, LPG-3400RS pump, WPS-3000TRS
autosampler
Right from top to bottom: FLD-3400RS fluorescence detector, UV detector
(VWD-3400RS or DAD-300RS), TCC-3000RS thermostatted column compartment
Tip: As the flow cell of the fluorescence detector has a pressure limit of 20 bar
(analytical flow cell) or 40 bar (micro flow cell), the fluorescence detector
must always be the last module in the fluidic path.
Refer to section 3.4.2 for information how to connect the USB ports on the rear panels.
Verify that Chromeleon is installed on the computer and that the license code is entered
before you connect the detector to the USB port on the Chromeleon computer and turn on
the detector power. Only if you install Chromeleon first, the detector is connected to the
computer and the USB driver for the detector is automatically loaded. The Windows®
operating system can detect the detector when the power is turned on.
Connect the detector to the Chromeleon computer via the USB port on the rear panel.
Select one of the following alternatives:
Tip: The USB standard limits the USB cable length to 5 meters. Each USB device
can be separated from the PC or next USB hub by no more than 5 meters.
The following cable is available (provided in the accessories kit for the detector):
USB cable, type A to type B, high speed USB 2.0 (cable length: 5 m) 6911.0002
Solvent rack
Pump
Autosampler
Column
compartment
Fluorescence
detector
Fig. 8: Example for the rear panel connections on an UltiMate 3000 system
Warning: Never use a power cord other than the power cords provided for the
device.
Do not use multiple sockets or extension cords. Using defective
multiple sockets or extension cords may cause personal injury or
damage to the device.
4. Slide the left guide bar of the DAC board onto the green edge next to the USB port.
USB port
Guide bar
5. Push the board partially into the enclosure. Apply slight pressure between the two
analog outputs to push the board further into the enclosure until it locks into position.
6. Attach the board to the rear panel, by using the 4 screws as shown in Fig. 9.
7. Connect the analog outputs to an evaluation device (→ page 35).
Tip: Installation of the DAC board does not require additional validation, such as
Operational Qualification or Performance Qualification.
Tip: When the detector is connected to the Chromeleon computer, verify that the
Chromeleon software is installed before turning on the detector power for the
first time. Only then, the USB driver for the detector is automatically loaded
and the Windows operating system detects the detector when the power is
turned on.
Tip: Clicking the Quit Monitor button quits (exits) the Server Monitor
program, but does not stop the server. To stop the server, click Stop.
6. Turn on the main power switch on the rear panel of the detector.
Windows XP
will automatically detect the new detector and launch the Found New Hardware
Wizard, which guides you through the USB installation. Select the following options:
a) If asked whether Windows can connect to Windows Update to search for software,
select No, not this time.
b) Accept the default option (Install the software automatically) and click Next>.
c) Click Finish when the wizard reports that the software for the detector has been
installed.
If Windows XP fails to detect the detector and a message box asks for a USB
configuration file (cmwdmusb.inf), this indicates that you connected the detector to
the computer and turned on the power for the first time before you installed
Chromeleon. To resolve the problem:
a) Click Cancel in the Windows message box.
b) Turn off the detector.
c) Install Chromeleon.
d) Turn on the detector power. Windows will now automatically detect the detector and
launch the Found New Hardware Wizard.
After the USB software for the detector has been installed (→ page 37), install and
configure the detector in Chromeleon:
1. Start the Chromeleon Server Monitor (→ page 37) and the Chromeleon server if they
are not yet running.
2. Start the Chromeleon Server Configuration program by clicking Start on the taskbar.
Point to Programs (or All Programs, depending on the operating system), point to
Chromeleon, and then click Server Configuration.
3. If necessary, click the plus sign next to the server name to display the items
underneath.
4. Select the timebase to which the detector will be assigned, or create a new timebase
(on the Edit menu, click Add Timebase).
5. Open the Add device to timebase dialog box. To do so, click Add Device on the Edit
menu or right-click the timebase and click Add Device on the menu.
6. On the Manufacturers list, click Dionex HPLC: UltiMate 3000 and on the Devices
list, click FLD-3x00(RS) Detector.
7. The configuration pages are opened. On each page, verify that the settings are correct
and select additional settings if needed. For a description of the pages, see
section 3.5.3.1.
8. Click OK to complete the configuration of the detector.
9. On the File menu, click Save Installation and then close the Server Configuration
program.
During the installation, Chromeleon connects to the detector and transfers the settings from
the instrument firmware to Chromeleon, setting the options on the wizard pages
accordingly. Verify that the settings are correct and make additional settings if needed.
You may reopen the configuration pages later again to change the settings (→ page 43).
Tip: Changing the settings for a specific application in the Commands dialog box,
in a program file (PGM), or on a control panel will not change the default
settings on the configuration pages.
For additional information about a page, click Help.
General Page
Shows the general instrument parameters.
• Virtual Mode
Verify that the virtual mode is set to off. If the virtual mode is enabled, the Module
Address box will be unavailable. If you exit this page without having entered a module
address, the virtual mode will be enabled automatically.
In the virtual mode, Chromeleon simulates detector control and data acquisition.
♦ Click Read to read and display data from an existing demo file instead of real data.
Select the file from the Virtual Mode File Name list.
♦ Click Write to save the data currently delivered by the detector as a demo file. Enter
the file name in the Virtual Mode File Name field or select a name from the list.
Tip: When recording virtual mode files in Chromeleon 6.80, the size of the file
is limited to 35MB. This corresponds to about 9 minutes at a data
collection rate of 100 Hz. If you want to record longer virtual mode files,
reduce the data collection rate.
• Module Address
Select the module address of the detector. Click Browse and then double-click the
detector that you want to use on the Device List. The address is automatically entered in
the Module Address field. Chromeleon connects to the detector and transfers the settings
from the instrument firmware to Chromeleon, setting the options on the pages
accordingly. Confirm the related message with OK.
• Download
Click this button to transfer the current detector configuration to Chromeleon. (The
button appears dimmed if the virtual mode is enabled.)
The detector is shipped with the most recent firmware version. If a firmware update is
ever required, follow the steps in section 7.6 (→ page 115).
Detector Page
The Detector page shows the detector configuration.
• FLD Type
Select the detector type. Make sure that the selected option corresponds to the actually
installed detector type.
• Device Name
Displays the name used to identify the detector the installation environment and in the
Chromeleon client program. To control the detector with the existing control panels,
accept the default name. If you enter a different name, you may have to re-link the
controls on the control panels and edit the device name in the program files.
• 2nd PMT
This check box must be selected if the optional red-sensitive Dual-PMT option for
measuring wavelengths up to 900 nm is installed.
• DAC Board
This check box must be selected if optional analog output are installed. (→ page 34)
Signals Page
The page lists all signal channels that the detector can record. A name is defined for each
channel. To allow raw data collection for a channel, select the Enabled check box next to
the channel name. If the check box is cleared, the detector cannot collect raw data for the
channel. To change a name, click in the field and overwrite the existing name directly in
the field.
1. No flow cell is installed when the detector is shipped. Install a flow cell (→ page 110)
and connect the cell inlet connection to the separator column outlet. Connect a waste
capillary to the flow cell outlet.
2. Connect the drain tubing (→ page 47).
3. Set up the detector in Chromeleon if it is not already set up (→ page 37).
4. Check and change the leak sensor setting if necessary (→ page 72).
5. Adjust the brightness and contrast of the detector display if necessary (→ page 72).
6. If you want to connect additional evaluation devices to the detector
Install the DAC plug-in board and configure the analog outputs (→ page 34).
7. Before using the module for sample analysis, equilibrate the entire system
(→ page 51).
Drain port
Fig. 14: Drain port
Direct liquid leaks to waste via the drain system of the UltiMate 3000 system, using the
components from the drain kit. The kit is shipped with the UltiMate 3000 pumps and can
be ordered separately (part no. 6040.0005). The kit includes all required components and
detailed installation instructions. If there is more than one detector in your system and you
need an additional tee piece, you can find one in the accessories kit of the fluorescence,
multiple wavelength, or diode array detector.
Optical block
• A cover is mounted on the flow cell opening when the detector is shipped. Keep this
cover in a safe place. If the detector is shipped or shut down for a longer time period,
reinstall the cover.
• Plugs are installed at the flow cell in and out connections (→ Fig. 19). Keep the plugs in
a safe place. If the detector or the cell is shipped or if the detector is shut down for a
longer time period, reinstall the plugs.
• Capillary connections between the column and flow cell should be as short as possible to
avoid peak broadening effects due to excessive dead volume.
• When connecting the flow cells, make sure not to invert input and output. This will
deteriorate the measured results and may destroy the flow cell due to the increased
backpressure in the cell.
• The backpressure on the flow cell must not exceed 20 bar (analytical flow cell) or 40 bar
(micro flow cell). Do not connect any capillaries or instruments to the flow cell out line
as this might generate a higher backpressure. Even if the pressure exceeds the upper limit
for a very short time only, the flow cell may be permanently damaged. If it is required to
connect a valve at the flow cell outlet, the valve may only be switched while the flow is
stopped. When switching valves while the flow is turned on, pressure peaks may occur
and destroy the flow cell. Thermo Fisher Scientific recommends using a capillary or tube
with an internal diameter of at least 0.5 mm at the flow cell out line.
1. Remove the cover on the flow cell opening (if installed). To do so, loosen the two
finger-tight screws. No tools are required to loosen the screws. The screws are captive
in the cover and do not need to be removed.
4. Remove the dummy plugs at the flow cell in and out connection ports. Connect the
flow cell inlet to the separation column. Connect the PEEK capillary from the
accessories kit for the detector as waste capillary to the flow cell outlet. Extend the
PEEK capillary with the silicone tubing (also included in the accessories kit for the
detector). Route the capillaries to the outside through the slots provided in the detector
enclosure to prevent them from being pinched when the front panel door is opened.
5. Close the front panel door to allow the firmware to detect the new flow cell.
6. Perform a wavelength calibration (→ page 90).
Mobile phase quality significantly affects detection limits and instrument performance. To
ensure optimal performance of the detector, observe the following guidelines:
• Prepare all mobile phases with HPLC-grade (or better) solvents, reagent-grade chemicals,
and filter HPLC-grade water. Usually, HPLG-grade solvents will provide good results.
As impurities in the solvents increase the baseline noise, you should use special
fluorescence-grade solvents, for example LiChrosolv®, for sensitive applications. Always
use fluorescence-grade solvents and water for Raman tests and instrument qualification.
• Degas all mobile phases before use and maintain them in a degassed state.
• Strong bases can etch the silica windows of the flow cell. Therefore, avoid the use of
mobile phases with a pH value > 9.5. In any case, disconnect the separation column and
flush the system with HPLC-grade water for 5°minutes at 1.0°mL/min immediately after
the analysis when alkaline solutions are used.
• Mobile phase pH affects not only the retention time of the separation, but the
fluorescence intensity and wavelength of the sample.
• When changing from a buffer to a different operating mobile phase, be sure the solvents
are miscible and will not induce precipitation of the buffers. Flush the cell with a buffer-
compatible solvent (in most cases, HPLC-grade water) immediately after the analysis. Do
not allow buffers to remain in the cell for extended periods.
For information about the properties of common used mobile phases, see section 10 in
Table 1 (→ page 123).
The pumping system should deliver continuous flow while ensuring intermixing of the mobile
phase (if gradient elution is used). Fluctuations in pump backpressure can cause baseline
noise. If the noise is synchronized with the pump stroke, check your HPLC pump.
The plastics present in some solvent delivery systems from third-party manufacturers are not
fully compatible with the solvents commonly used in chromatography. Therefore, plastic
components may dissolve, and thus impair fluorescence detection.
For UV wavelengths, these guidelines are recommended:
• The mobile phase reservoir should be glass.
• All tubing connections should be made of materials suitable for HPLC applications (for
example, PTFE, ETFE, PEEK, stainless steel, or titanium), as required for the operating
pressures and application.
• Some pump seals incorporate a band spring to preload the seal during the vacuum stroke
of the piston. The band spring should be made of stainless steel, a fluoropolymer
(perfluoroelastomer or fluorosilicone), or another material of known quality.
If you are working with an UltiMate 3000 system, using original Dionex parts only, all the
above recommendations are met.
To ensure optimum performance of the flow cells, observe the following guidelines:
• The backpressure on the flow cell must not exceed 20 bar (analytical flow cell) or 40 bar
(micro flow cell). Do not connect any capillaries or instruments to the flow cell out line
as this might generate a higher backpressure. Even if the pressure exceeds the upper limit
for a very short time only, the flow cell may be permanently damaged. If it is required to
connect a valve at the flow cell outlet, the valve may only be switched while the flow is
stopped. When switching valves while the flow is turned on, pressure peaks may occur
and destroy the flow cell. Thermo Fisher Scientific recommends using a capillary or tube
with an internal diameter of at least 0.5 mm at the flow cell out line.
• When connecting the flow cells, make sure not to invert input and output. This will
deteriorate the measured results and may destroy the flow cell due to the increased
backpressure in the cell.
• The contacts for the flow cell identification chip and the temperature control are located
on the rear of the flow cell. To ensure proper functionality, be careful not to touch the
sensitive electronics. If liquid comes into contact with the electronics, dry it immediately.
• During longer idle times, the flow cell should not be filled with pure water to avoid the
growth of algae. Add 10% HPLC-grade isopropyl alcohol, for example, and plug the
flow cell input and output using the plugs that were installed when the flow cell was
shipped (→ Fig. 19). Using different plugs and tightening them may destroy the flow
cell.
• If a flow cell leaks, remove the flow cell from the detector as quickly as possible, and
replace the flow cell.
• For information about how to clean a flow cell, see page 109.
5.1 Power-Up
To start the detector for the first time, turn on the main power switch on the rear panel of
the detector. The following sequence of events occurs when the detector is powered up
• For a short time, general information about the detector appears on the display: device
type, firmware version, and serial number.
• The detector runs a series of internal tests. (The test takes about 30 seconds.) During
these self-diagnostics, all of the main components are checked. When the self test was
successful, the initial screen changes to the status screen (→ page 55).
• If an error is detected, the detector is not ready for analysis. The Status LED on the front
panel is red and a message appears on the front panel display. If the detector is operated
with Chromeleon, the message appears also in the Chromeleon Audit Trail. Turn off the
detector, take appropriate remedial action (→ page 97), and turn on the detector again.
• If the message "Not calibrated" appears, verify that a flow cell is installed and execute the
Calibrate command in Chromeleon.
For routine operation, leave the main power switch on. For routine on/off control, use the
standby button on the front of the TCC (→ page 21). Press and hold the button for about
one second to allow the detector to change the mode. Turn the main power switch off when
instructed to do so, for example, before performing a service procedure.
FLD-3400RS
Ex: Em:
Off
244 400
HighPower
nm
RT: 2.3 FW 280nm Sens 7
nm
You can adjust the screen brightness or screen contrast to your requirements from
Chromeleon or on the detector display (→ page 72).
FLD-3400RS
71289
@ wavelength
Ex 250 nm
Em 350 nm
Run HighPower RT: 2.3 FW 280nm Sens 7
FLD-3400RS
1: Ex 220 nm 2: Ex 225 nm
46843 Em 325 nm 34352 Em 315 nm
3: Ex 237 nm 4: Ex 244 nm
25146 Em 460 nm 19272 Em 400 nm
MultiChannel HighPower RT: 2.31
Fig. 21: Data acquisition screen (examples)
For information about the menus, see section 5.3.1 (→ page 58).
Four white spots can be found on the front panel below the display. To show the keys,
touch the position of the utmost left spot on the display with the menu pen (part
no. 6300.0100). The menu pen is included in the accessories kit for the UltiMate 3000
autosampler.
The menu key replaces the information in the bottom line of the status screen. Select the
utmost left spot again to call the main menu. If no key is selected, the bottom line of the
status screen is restored after about 5 seconds.
FLD-3400RS
Ex: Em:
Menu
244 400 nm nm
If the detector is connected with Chromeleon, settings that do not interfere with the
measurement, such as, the screen brightness or contrast, can still be changed from the
display.
Fig. 24 shows an overview of the detector menus. For information about the general menu
layout and structure, see page 59. For information about the individual commands and
parameters, see sections 5.3.3 through 5.3.5 (→ page 61 and following pages).
Main
3 ∨ ∧ Select Back
No. Description
1 Reports the menu name and the number of items on the menu list.
2 The menu items appear on a list and are numbered consecutively.
The selected item is underlined.
3 Navigation bar
Select an item with the arrow up or down key—the selected item is underlined. Confirm
your selection with Select. Back returns you to the previous menu level.
The selected menu item or parameter determines which function keys appear on the
navigation bar:
To … Select ...
To … Select ...
Toggle between two operating states (for example, between Silent and Audible in the Toggle
Leak sensor mode).
Confirm the selection and perform the action. OK.
For example, if you change the brightness of the display, you have to select OK to
confirm the change.
Cancel the action and restore the last value. Cancel
For example, if you have changed the brightness of the display, select Cancel to undo
this action and to restore the previous operating state.
Note: Depending on the selected option, specific keys may replace these general keys.
If an error is found, one or more messages appear on the front panel display. In this case,
the Prev, Next, and Clear keys appear on the navigation bar.
To … Select ...
The Main menu provides top-level access to the menu structure. To open the Main menu,
show the function keys and select Menu (→ page 57).
∨ ∧ Select Back
Fig. 26: Main menu
Select an item with the arrow up or down key—the selected item is underlined. Confirm
your selection with Select. Back returns you to the status screen.
For information about the menus, see
The Configuration menu provides information about the detector configuration and allows
you to make the required settings or change the settings.
∨ ∧ Select Back
To … Select …
Reset all important detector settings to the standard settings. In the Reset to factory defaults
Reset to factory defaults? dialog box, select OK to confirm the restore
or select Cancel to keep your settings.
Set the display and function key parameters: Display & soft keys
Brightness—sets the screen brightness.
Contrast—sets the screen contrast.
Key sound—sets whether a beep sounds when you select a function
key: On—yes or Off—no.
Key autorepeat—sets whether the keystroke is automatically repeated
when you remain on the key for a longer period, for example, to change
a value quickly (On = yes or Off = no).
Set how you are alerted in case of a leak alarm: Leak Sensor Mode
Audible—activates the leak alarm. When a leak is detected, a beep
sounds.
Silent—deactivates the leak alarm. When a leak is detected, a message
appears on the front panel display, but no beep sounds.
∨ ∧ Select Back
To … Select …
View information about the detector, such as detector type and firmware version. System
Check whether a second, red-sensitive PMT is installed. Optics
View information about the flow cell, such as, serial number, flow cell type, and Flow Cell
flow cell material.
View information about the temperatures inside the detector Temperatures
The Service menu provides information for authorized service personnel when exchanging
certain components.
1. The Chromeleon software is installed on the computer and the license code is entered.
2. The detector is connected to the Chromeleon computer via a USB connection.
Tip: Verify that Chromeleon is installed on the computer and that the license
code is entered before you connect the detector to the USB port on the
Chromeleon computer and turn on the detector power. Only then, the USB
driver for the detector is automatically loaded and the Windows operating
system can detect the detector when the power is turned on.
3. The detector is set up in Chromeleon, as described in section 3.5 (→ page 37).
Before you can operate the detector with Chromeleon, you have to connect the timebase in
which the detector is installed to the Chromeleon client program (→ page 64).
Two modes of software control are available:
• Direct control with the parameters and commands from the Commands dialog box
(→ page 65) or from a control panel (→ page 66).
• Automated control with a control program (PGM) (→ page 67).
1. Start the Chromeleon Server Monitor and the Chromeleon server if they are not yet
running (→ page 37).
2. Start the Chromeleon client by clicking the Chromeleon icon on the desktop.
If the Chromeleon icon is not on the desktop, click Start on the taskbar, point to Programs
(or All Programs, depending on the operating system), point to Chromeleon, and then
click Chromeleon.
3. Connect the Chromeleon client program to the timebase in which the detector is
installed. For details about how to do this from the Commands dialog box, see
page 65. For details about how to do this on a control panel, see page 66.
With direct control, you select operating parameters and commands in the Commands (F8)
dialog box. Direct commands are executed as soon as they are entered. For routine
operation, most parameters and commands are available also on a control panel.
Tip: Manual acquisition from the Commands dialog box is only supported for one
channel. The Multi-Channel Mode is not available.
5. Change the display filter level if necessary. Right-click in the commands list and select
the filter level on the menu.
2. On the Panel Tabset for your timebase, click the page for the detector.
3. Verify that the detector is connected to Chromeleon (the LED next to the Connect
button is green). If it is not, click Connect.
The control panel provides access to the operating parameters and commands required for
routine operation of the detector. Additional functions are available in the Commands
dialog box. To open the Commands box from the panel tabset, select Command on the
Control menu.
In addition to programs for sample analysis, you can also create programs for special
purposes, for example, to automate system shutdown (→ page 94) or to ensure that the system
automatically restarts operation as desired after a power failure. For details, see the
Chromeleon Help.
When you record multiple channels (FLD-3400RS only), the baseline noise increases at
higher data collection rates. The maximum data collection rate and response time depend
on a number of parameters and are always automatically calculated on the basis of the
selected parameters. In the Multi Channel Performance box, select a measuring
performance (→ page 87).
In addition, you can define the flow cell temperature (→ page 88) and the allowed
deviation.
Tip: In Multi-Channel Mode, the selected lamp mode is always HighPower.
3. After you finish the wizard, Chromeleon automatically creates the corresponding
program.
4. To start the program, follow the steps below (→ page 71).
Opens the
Commands
View
Open the
Device
Views
Fig. 33: Chromeleon program file (here program shown in the Commands view)
To start a program
Program for sample analysis
1. Create a sample list (sequence). A sequence must include the program and a method
for evaluating the sample data (for example, for peak identification, area
determination, and amount determination).
2. Assign the program and method to each sample on the list.
3. Add the sequence to the batch and start the batch.
For information about each of the above steps, see the Chromeleon Help.
Other programs
Add the program to the batch and start the batch.
The SmartStartup wizard assists you in automating regular routine tasks (→ page 51).
With SmartStartup, the different modules of the UltiMate 3000 system are turned on
automatically and in a controlled manner. For the fluorescence detector, for example,
SmartStartup turns the flow cell heating on. In addition, SmartStartup can purge the pump
of the HPLC system automatically, flush the column, and perform system equilibration.
Important module parameters are monitored. When the modules operate within these
limits, the sample sequence, which was set up before, can be started automatically.
SmartStartup can be used at any time.
If you have to interrupt system operation, use the SmartShutdown wizard to create a program
to set the HPLC system into standby mode or to automate shutdown of the system
(→ page 94).
Leak detection is enabled as a standard when the detector is shipped. When leak detection
is active and the leak sensor reports a leak
• The Status LED on the front panel door is red.
• A message appears in Chromeleon and on the detector display.
• The Leak property in Chromeleon is set to Leak_Detected.
• A beep alerts you.
When the leak sensor reports a leak, eliminate the cause for the leakage and dry the leak
sensor (→ page 113). If the leak is not eliminated immediately, Chromeleon aborts the
running batch.
Disabling leak detection (not recommended):
In Chromeleon, open the Commands dialog box for the detector and set LeakSensorMode
to Disabled.
Disabling the leak alarm
Call the Configuration menu on the detector display and set the Leak sensor mode to Silent.
When a leak is detected, a message appears on the front panel display, but no beep sounds.
You can adjust the screen brightness or screen contrast to your requirements from
Chromeleon or on the front panel display.
Tips: In Multi-Channel Mode, you cannot directly select the Response Time and
Data Collection Rate, as these parameters are determined automatically
(→ page 87) and adjusted accordingly when wavelengths are switched during
the measurement.
In Multi-Channel Mode, the selected lamp mode is always HighPower.
Manual acquisition from the Commands dialog box is only supported for one
channel.
In Zero Order Mode, the grating of the emission monochromator is set to the position of
zero order. In this position, the monochromator lets the entire spectrum pass, rather than
only a certain wavelength. The excitation monochromator is set to one wavelength as
usual. The FLD-3400RS allows you to cut off undesired wavelengths using the filter wheel
setting (→ page 85). To activate the Zero Order Mode in Chromeleon, set the
EmWavelength property to ZeroOrder.
Use this mode during method development, if you do not know the retention times of the
various substances in your sample. As the entire range of emission wavelengths is acquired,
you can determine the retention times of all substances in a single run.
The Zero Order Mode is also suitable for samples that emit light at a broad spectral
bandwitdh. In this case, the measured intensity is higher in Zero Order Mode than under
normal operation. This allows you to measure samples with a lower concentration.
5.6.4 2D Scans
With the FLD-3x00(RS) detectors, you can also record several types of 2D spectra. The
excitation monochromator or emission monochromator (or both simultaneously) moves
over a settable wavelength range, while the intensity of the fluorescence signals is
measured and recorded continuously for each wavelength. This allows you, for example, to
record spectra for determining the optimum emission and excitation wavelengths.
During all scans, stop the pump flow or pump at a very low flow rate to achieve stable
conditions in the flow cell of the fluorescence detector.
A baseline spectrum with the same parameters can be recorded for all scan modes. The
baseline spectrum is stored and automatically subtracted from the recorded spectra. The result
is a difference spectrum. If the parameters for a scan change, the background spectrum is
automatically deleted and a new spectrum must be recorded. You can delete a baseline
spectrum any time by using the ClearBaseLine command.
Chromeleon automatically saves the spectra, including the baseline spectrum, to a spectra
library named FLD3000.LIB. The spectra library is saved in the timebase directory on the
local data source. If a scan is performed during sample processing, the library is saved in the
associated sequence.
Excitation Scan
The wavelength on the emission monochromator is kept constant, while the excitation
monochromator scans a wavelength range. The result is an excitation spectrum of the
sample.
Emission Scan
The wavelength on the excitation monochromator is kept constant, while the emission
monochromator scans a wavelength range. The result is an emission spectrum of the
sample.
Synchro Scan
Tips: During the scan process, no other commands can be sent to the fluorescence
detector.
The duration of the scan process depends on the range to be scanned and the
selected scan speed.
Before each scan, select a detector sensitivity, using the ScanSensitivity
command (→ page 81).
Artefacts may occur when scanning near extreme changes in the spectrum
(which frequently occur near the excitation wavelength), for example, when
scanning the Raman emission spectrum of water near the excitation of 350 nm.
In this case, select a greater distance between the wavelength scan range and
the edge. For the Raman emission scan, for example, select a start wavelength
of 385 nm.
Manual spectra scans are supported under Chromeleon 6.80, but are currently
not supported under Chromeleon 7.1 or later.
Complete the following steps to record an excitation spectrum:
1. Open the Commands dialog box for the detector. Under ScanStartExWavelength,
enter the first wavelength of the range to be scanned and the last wavelength under
ScanEndExWavelength. Select an emission wavelength (ScanStartEmWavelength)
and a scan speed (ScanSpeed).
2. Stop the pump flow (Flow=0) or set it to a very low flow rate.
3. Execute the ScanExcitation command.
From Chromeleon 7.1 on, 3D scanning is supported for the FLD to facilitate determining
the retention times and absorption maxima. As opposed to 2D scans, where the selected
spectral range is scanned once, the spectral range is scanned continuously, resulting in a
spectral field similar to a 3D field of a diode array detector. As for 2D scans, 3D scan
modes include excitation scan, emission scan, and synchro scan.
Instrument methods must be used for recording the spectra. In the Instrument Method Wizard,
select the 3D Data Acqusition on option. All required parameters can be set on the FL Field
Settings page of the wizard. During a 3D scan, no emission channels can be recorded.
The recorded 3D data are represented as a 3D data field in the Contour Plot. Use the 3D data
field to determine the retention times and optimum emission or excitation wavelengths.
For more information about 3D data fields, see the Chromeleon 7.1 (or later) Help.
In Chromeleon, you can set the operating parameters manually in the Commands dialog
box for the detector (→ page 65) and on the page for the detector of the Panel Tabsets
(→ page 66). When you create a program with the Program Wizard, you can enter most
parameters on the FLD Options page (→ page 68).
The most important parameters that need to be optimized are the excitation and emission
wavelength. Note the following key criteria for determining the wavelength for an
analysis:
• Preferably, select an excitation wavelength on the absorption maximum of the sample
components.
• The mobile phase should be "transparent", showing little or no absorption, at the selected
wavelength. Thus, the excitation wavelength should always be above the UV cutoff of
the solvent (→ table page 123).
• Select an emission wavelength that is at least 20 nm above the excitation wavelength.
The following section outlines two methods to determine the optimum wavelengths. After
you have determined the optimum wavelengths and the retention times, you should perform
another analysis run using these parameters to determine a suitable sensitivity (→ page 81).
Method using 2 samples of different concentrations with a diode array detector and the
fluorescence detector
1. Use a sample with a concentration that is suitable for diode array detectors (for
example, 100 ng/µL) and run an analysis with the DAD, recording a 3D field. You can
extract the retention times and absorption maxima, and thus the optimum excitation
wavelengths, of each sample component from the Chromeleon 3D plot (→ Fig. 34,
page 79).
2. Use a sample with a concentration that is suitable for fluorescence detectors (for
example, 100°pg/µL for high-fluorescing substances) and run an emission scan for
each sample component with the FLD, using the retention times and excitation
wavelengths. Note that you may have to add a time offset between the DAD and FLD
when determining the retention times if the two detectors are connected in series. You
will get the optimum emission wavelengths (largest peak) for each sample component.
Absorption-
maximum
peak 2
Tip: Chromeleon 7.1 (or later) supports 3D spectra scanning for the FLD, which
facilitates determining the retention times and absorption maxima without a
diode array detector (→ page 76).
Background
A PMT (or optionally two PMTs) measures the intensity of the emission light after the
emission monochromator. The sensitivity of the PMT can be adjusted in 8 steps (1 to 8) with
the Sensitivity parameter. With each step, the sensitivity of the PMTs increases by
approximately a factor 2. If a peak with sensitivity = 5 is 15 million counts high, for example,
the peak height increases to 30 million counts when the sensitivity = 6 (→ Fig. 35).
• If the selected sensitivity is too small, the peak height is reduced and the signal-to-noise
ratio is not optimal (→ Fig. 35, Sensitivity = 1).
• If the selected sensitivity is too large, the PMT signal is saturated. In this case, the
detector automatically reduces the sensitivity. Lines appear in the chromatogram at the
beginning and at the end of the saturation (→ Fig. 35, Sensitivity = 8). If the detector is
not saturated any more, the Sensitivity setting before saturation is restored.
Tips: When the sensitivity was automatically reduced or when the initial value was
restored, the Chromeleon Audit Trail shows a warning with the new sensitivity
value after the adjustment.
Calibration depends on the PMT. Therefore, calibration and quantification
must always be performed with the same PMT.
Determine the optimum sensitivity in a separate sample run after you have determined the
optimum wavelengths (→ page 78). Use a sample (standard) with the maximum expected
concentration of the analytes and select a sensitivity at which a saturation is not expected
(for example; 1 or 2). If the peak heights of the individual peaks in a chromatogram differ,
you can improve the signal-to-noise ratio of the smaller peaks by switching the sensitivity
during the run. You can select the Sensitivity for all channels directly in the Program
Wizard (→ page 68).
With the FLD-3x00(RS), the intensity of the emission light (measured by the PMT) is
normalized with the intensity of excitation light through the sample (measured by the
reference diode). Therefore, the values (counts) that the emission channel displays cannot be
used for optimizing the sensitivity. In Fig. 35 the PMT is saturated at 63 million counts.
However, under different measuring conditions, the PMT may be saturated at a value of
100 million counts, for example.
1. Open the program you want to optimize in the Commands View. The required
commands must be added to the program manually.
2. Add a Log command for the MaxPMTSaturation property after the peak maximum
of an expected peak (or group of peaks) to log the maximum saturation value at this
time in the Audit Trail (→ Fig. 36).
3. Add a ClearMaxPMTSaturation command shortly after, before the next peak elutes,
to reset the MaxPMTSaturation value to zero (→ Fig. 36).
4. Repeat steps 2 through 3 for all peaks.
Run a sample and read out the MaxPMTSaturation values in Chromeleon and evaluate
the results:
If you do not know the expected concentrations of the analytes, reduce the Sensitivity even at
smaller values of MaxPMTSaturation.
Tips: The maximum saturation shown with MaxPMTSaturation affects the signals
of both PMTs with the parameters of all channels.
You can completely turn off fluorescence detection by setting the sensitivity to
Off. This may be required, for example, if you want to record the incoming
signal from a UV detector for a sample of high concentration, or to suppress an
extremely high peak that is not of interest for you but triggers an automatic
adjustment of the sensitivity.
To prevent this stray light from reaching the PMT, additional optical edge filters are
installed in the light path between the flow cell and the emission monochromator. This
reduces direct scattering of light from the light source. In addition, a grating
monochromator lets unwanted fractions (the half, one third, ...) of a selected wavelengths
pass. If the monochromator is set to 500 nm, for example, second-order stray light at 250
nm from the sample may reach the PMT. The filters also eliminate this higher-order stray
light.
Ideally, these filters let all wavelengths above their cut-off wavelength pass, while light with a
smaller wavelength than the cut-off wavelength is blocked. In practice, there is a transition
area where the transmission of the light increases from the lower wavelengths near the range
where the light is cut off to the higher wavelengths near the range where the light passes.
Fig. 37 shows the transmission behavior of the 280 nm filter, which is the filter that is
installed in the FLD-3100 before the emission monochromator.
The FLD-3400RS provides a filter wheel that is located before the emission monochromator.
The filter wheel carries several optical filters with different cut-off lengths. The qualitative
transmission behavior of all filters is shown in Fig. 37, with a transmission range of approx.
+/- 30 nm. At the cut-off wavelength, the filters let 50% of the light pass. The filter wheel
setting can be selected automatically or manually.
• If the filter wheel mode is set to Auto, the detector automatically selects a filter wheel
position. It selects the first filter with a cut-off wavelength below the selected emission
wavelength. This mode is selected by default and provides best results for most
applications.
• You can manually select the filter wavelength. Available filters are 280 nm, 370 nm,
435 nm or 530 nm. The selected emission wavelength must not be more than 15 nm
below the filter wavelength. In special situations (for example, if the emission
wavelength is near the cut-off wavelength of a filter), setting the filter manually may
provide better results than the Auto setting.
If you select Open, the filter wheel remains in an open position. Use this setting if you
want to measure with an emission wavelength between 220 nm and 280 nm.
Manually select the filter wheel position, for example, in combination with the Zero Order
Mode. The emission monochromator opens and the emitted light is measured over the entire
wavelength range. Use the cut-off filter to suppress light below the wavelength you are
interested in. Note that this setting usually requires a lower Sensitivity setting due to the stray
light and auto fluorescence of the eluent (the entire spectral range is recorded).
You can select the filter wheel setting for all channels directly in the Program Wizard
(→ page 68).
For further information about selecting the filter wheel setting, refer to the Fluorescence
Method Development Handbook that is shipped with the detector.
Tip: In Multi-Channel Mode, you cannot directly select the Response Time and
Data Collection Rate, as these parameters are determined automatically
(→ page 87).
The response time is a measure of how quickly the detector responds to a change in signal.
The data collection rate is the number of data points per second (Hz) that Chromeleon
collects from the detector and stores as raw data.
The Program Wizard in Chromeleon automatically calculates the appropriate response time
and data collection rate, based on the value you enter for the peak width at half-height
(→ Fig. 31, page 68). If you want to select a different response time and data collection rate,
note the following guidelines:
Response time
• Select a response that is about 1/3 of the peak width at half-height of the narrowest peak
of interest. A longer response time allows more averaging of the signal and results in less
short-term noise.
• However, if the selected response time is too long, this can result in reduced peak heights
and asymmetrical peak shapes. Peaks that elute shortly after each other may not be
separated properly. When set correctly, the response time significantly reduces baseline
noise, but reduces peak height only slightly.
As the fluorescence of a sample decreases as temperature increases, the temperature must not
be selected too high. However, it must be above the temperature inside the detector optics,
which is influenced by the ambient temperature. Therefore, select a temperature that is
roughly 15°C above the expected ambient temperature.
Example: The expected maximum temperature in the laboratory is 27°C (80.6 F). Set the
flow cell temperature to 42°C (107.6 F).
Use the Program Wizard to define the flow cell temperature and the allowed deviation
(→ page 68).
The FLD offers three different modes for the xenon flash lamp:
• In HighPower mode, the lamp flashes at the highest frequency. This mode is
recommended for applications that require highest sensitivity. It is selected automatically
when you are recording multiple wavelength channels. The sensitivity is roughly twice
the sensitivity in Standard mode. The expected lifetime of the lamp is approximately
1300 hours. (Only the time during data acquisition is counted.)
• In Standard mode, the lamp flashes at a medium frequency. This mode is recommended
for applications that require a high sensitivity. The expected lifetime of the lamp is
approximately 4000 hours. (Only the time during data acquisition is counted.)
• In LongLife mode, the lamp flashes at a lower frequency. When the xenon lamp is
operated in this mode, the lamp life is approximately four times the lifetime in Standard
mode. However, note that signal-to-noise ratio is reduced to roughly the half. The
expected lifetime of the lamp is approximately 16000 hours. (Only the time during data
acquisition is counted.)
This mode only supports data collection rates up to 20 Hz. If you select the LongLife
mode and a data collection rate higher than 20 Hz, the data collection rate will be
automatically reduced.
You can select the Lamp Mode directly in the Program Wizard (→ page 68) if you have
selected a single wavelength channel.
Tip: You can change the lamp mode during a measurement, for example, from
LongLife mode (between the peaks) to Standard or HighPower mode (for the
interesting peaks). This extends the lamp lifetime, without any loss in
sensitivity in the important areas. For further information about the modes for
the Xenon lamp, refer to the Fluorescence Method Development Handbook for
the detector.
If wavelengths are switched or the sensitivity, filter wheel, or PMT setting are changed
during a program, the chromatogram may show baseline jumps. You can define how the
baseline behaves in these cases. Select whether you want to automatically perform an
autozero (Zero), to append the baseline to the previous signal (Append), or to let the
baseline "jump" to the new value (Free).
Tip: Using the AutoZero command, you can perform an autozero any time, that is,
the intensity measured at the time of the autozero is subtracted from any
intensities measured thereafter. Always select a time at which no sample flows
through the cell to perform an autozero. The values are stored and can be reset
using the ClearAutoZero command.
For information about how to monitor the remaining lamp lifetime, refer to section 7.2
(→ page 108).
A simple calibration procedure is performed after power-up of the detector. This requires
that a flow cell is installed in the detector. During the calibration process, ensure that the
eluent composition in the flow cell does not change and no air bubbles are present in the
flow cell. If the message "Not calibrated" appears when the detector is turned on, verify
that these conditions are met and execute the Calibrate command in Chromeleon.
In addition, you can verify the wavelength calibration using water (Raman measurement). If
verification fails, that is, if the calibration shows a significant deviation, you can perform a
wavelength calibration using water (Raman measurement). During wavelength calibration,
the light spectrum of the xenon flash lamp is used to calibrate the excitation wavelength.
Afterward, the emission monochromator is adjusted with the help of the maximum of the
Raman emission spectrum (379 mm).
The following conditions must be met for both wavelength verification and Raman
wavelength calibration:
• The system is equilibrated and environmental conditions are stable.
• There are no air bubbles in the flow cell. We recommend degassing the water. Set a flow
rate of 0.5 mL/min and wait about 15 minutes before you begin, until the baseline is
stable.
• The water has no impurities. Always use fluorescence-grade water and consider using a
filter or a suitable column before the detector.
Confirm with OK if you are sure that the above conditions are met.
The result (passed/failed) is displayed in the Chromeleon Audit Trail.
Passed: The calibration accuracy is within the allowed deviation range. The exact
wavelength can be found under RamanValidationWL. The ideal value for the
measurement is 397 nm.
Failed: The calibration of the detector is not sufficient. Perform a wavelength calibration
(→ page 91). If wavelength verification fails again after the recalibration, check the
causes and remedial actions outlined in section 6.3 (→ page 102).
Wavelength Calibration
You can perform wavelength calibration via Chromeleon. Wavelength calibration can take
a few minutes. During this time, data acquisition is not possible.
1. Open the Commands dialog box for the detector.
2. Select CalibrateRaman to start the calibration. The following message appears in
Chromeleon:
Make sure that
- the system is equilibrated and conditions are stable
- fluorescence-grade water is flowing through the cell
- the water is degassed (no air bubbles) and free of particles
Confirm with OK if you are sure that the above conditions are met.
3. The new calibration values are stored in the detector.
4. Perform wavelength verification.
The FLD_FlowCell channel for recording the flow cell temperature is available in the
Commands dialog box for the detector and on the FLD Options page in the Program
Wizard (→ page 68).
Thermo Fisher Scientific recommends always recording the flow cell temperature. If a
problem occurs, the temperature channel can provide helpful information to identify and
eliminate the source for the problem.
These commands reset the related counters and update the information when the action
was performed.
Control Panel
On the control panel for the detector, click Wellness, Qualification, and Service to see the
related predictive performance commands and parameters on separate panels. You can define
limits and grace periods for service and qualification intervals. In addition, wellness bars
provide visual indicators of qualification and service periods.
Color Description
Green Ok
Yellow The value will soon reach the specified limit and/or the related component needs
servicing or should be replaced soon.
Orange (Only for monitoring Qualification properties.) The value has reached the specified
limit. However, a Grace Period has been specified during which the component may still
be operated.
Red The value has reached the specified limit. Replacement, servicing, or qualification of the
detector is overdue. The detector can no longer be operated Besides, it is not possible to
start a batch.
Standby Program
A standby program sets the HPLC system into standby mode. The application can be
reactivated very quickly afterward. The pump flow is automatically reduced at the end of the
program, and the temperature of all temperature-controlled system modules, for example, the
FLD flow cell heating, can be reduced or the temperature control turned off.
Shutdown Program
A shutdown program automates shutdown of the HPLC system. The pump flow is
automatically stopped at the end of the program. Certain system components and functions
are turned off (for example, detector lamps, temperature control of the column oven or FLD
flow cell heating).
For more information about the SmartShutdown wizard, see the Chromeleon Help.
Perform the maintenance procedures listed in the table at regular intervals to ensure optimum
performance and maximum uptime of the detector. The exact maintenance schedule for the
detector will depend on a number of factors.
6 Troubleshooting
6.1 Overview
The following features help you to identify and eliminate the source for problems that may
occur during the operation of the detector or UltiMate 3000 system.
Status Screens
The status indicators on the front panel provide a quick visual check of the operational status
of the detector. They indicate whether the detector is turned on, connected in Chromeleon,
and operating properly (→ page 21).
Error Messages
If a fault or error is detected during the operation of the detector, a message appears on the
detector display. Check the Messages on the Detector Display section for recommended
courses of action (→ page 98). If the detector is operated by Chromeleon, a message is also
displayed in the Chromeleon Audit Trail.
Tip: For information about operating problems that might occur during the
operation of an UltiMate 3000 system, see Operating Problems (→ page 102).
If you are unable to eliminate a problem following the instructions given here, contact the
Thermo Fisher Scientific Service for Dionex HPLC products.
To … Select …
These keys are active also when the detector is connected with Chromeleon.
If the detector is connected with Chromeleon
• The message is also displayed in the Chromeleon Audit Trail.
• Messages on the front panel display can be removed also via the ClearDisplayError
command in Chromeleon.
The following table lists the most important detector-related messages along with
recommended remedial actions. In addition to the messages in the table, other messages may
appear. In this case, note the exact wording of the message and contact Thermo Fisher
Scientific Service for Dionex HPLC Products if you are unable to eliminate the problem.
Command rejected - Wait until the detector has executed the active command and retry.
device is busy.
Command rejected - The detector was turned off by the Standby button. Turn on the detector
device standby. and try again.
Data not available Verify that the flow cell is properly installed. Open and close the front
panel door. Turn the detector off and on again by pressing the power
switch on the rear of the detector.
Download failed. The firmware download failed. Repeat the firmware download.
Download firmware Verify that you have selected the correct firmware file. Repeat the
mismatch. firmware download.
Flow cell found. A new flow cell was found. It is recommended to perform a wavelength
CalibrateRaman calibration (→ page 91); without calibration, wavelengths may deviate
recommended. from the actual wavelength by up to a few nanometers.
Flow cell ID chip not Verify that the flow cell is properly installed. Open and close the front
found. panel door. Turn the detector off and on again by pressing the power
switch on the rear of the detector.
Flow cell temperature Verify that the flow cell is properly installed. Open and close the front
sensor not found. panel door. Turn the detector off and on again by pressing the power
switch on the rear of the detector.
ID bus controller error Turn the detector off and on again by pressing the power switch on the
rear of the detector.
ID bus short circuit Remove the flow cell. Turn the detector off and on again by pressing the
detected. power switch on the rear of the detector. If the error occurs again with the
flow cell installed, contact Service.
Internal hardware Turn the detector off and on again by pressing the power switch on the
configuration failure. rear of the detector.
Invalid PMT selection for You cannot select both PMTs (PMT1 and PMT2) for excitation scans.
excitation scan. Select either the standard (PMT1) or the infrared (PMT2) PMT.
Leak detected. The leak sensor has reported a leak. Check the flow cell for indications of
leakage. Retighten leaking connections if necessary. Dry the leak sensor
(→ page 113).
Leak detected - eliminate The leak sensor has reported a leak. Check the flow cell for indications of
within approx. x seconds. leakage. Retighten leaking connections if necessary. Dry the leak sensor
(→ page 113).
Memory failure - flash The firmware download failed. Repeat the firmware download.
access error.
No flowcell found. Verify that the flow cell is properly installed. The lamp is automatically
turned off when a flow cell is missing.
Not calibrated. The detector is not calibrated. Verify that a flow cell is installed correctly
and that the eluent composition in the flow cell does not change and no
air bubbles are present. Then open and close the front panel door.
Overflow - scan data Signal overflow. Repeat the scan with a lower sensitivity.
invalid.
Qualification interval The qualification interval will expire after the number of days indicated
warning % days in the message. Perform a qualification.
remaining.
Qualification out of date The qualification interval has expired. Perform a qualification.
or missing.
PMT Autorange for The detector was unable to perform autoranging (the automatic reduction
<CHANNEL> ignored, of the sensitivity when the detector becomes saturated), as the Sensitivity
(...). was changed manually at the same time.
PMT sensitivity autorange The detector had to automatically reduce the Sensitivity. Select a suitable
for <CHANNEL> -new Sensitivity (→ page 81) and repeat. The Chromeleon Audit Trail shows a
sensitivity is x. warning, in which x indicates the new sensitivity value after the
adjustment. Use this value in your method when you expect similar
concentrations.
PMT sensitivity change The Sensitivity was changed manually during autoranging (the automatic
aborted autorange for reduction of the sensitivity when the detector becomes saturated).
<CHANNEL>.
PMT sensitivity restored The Sensitivity was restored to the initial value (= x) after automatic
for <CHANNEL> - new adjustment.
sensitivity is x.
Scan command with equal Enter a different start and end time for the wavelength scan range.
start and end position.
Service interval expired. The service interval has expired. Have authorized service personnel
perform system maintenance.
Service interval warning - The service interval will expire after the number of days indicated in the
% days remaining. message. Have authorized service personnel perform system
maintenance.
Signal overflow in The reference signal is too low (high absorption, high PMT signal).
channel xxx. Check if the flow cell is contaminated. Consider cleaning or replacing the
flow cell. Check if the eluent concentration is too high. The lamp may be
too old and may have to be replaced.
System fan operation Turn the detector off and on again by pressing the power switch on the
failure. rear of the detector.
System overtemperature Verify that the ventilation slots on the side panels are not obstructed, and
detected. that there is sufficient clearance behind and to the sides of the detector for
ventilation. Reduce the room temperature, if necessary.
FLD-3100@USB-1610103 - The USB connection between the detector and the Chromeleon server
Device not found on the USB. may be interrupted. Check the USB connection.
The power supply to the detector may be interrupted. Check the power
supply connection of the detector.
Error opening FLD-3100 The USB connection between the detector and the Chromeleon server
@USB-1610103 – The System may be interrupted. Check the USB connection.
cannot find the file specified The power supply to the detector may be interrupted. Check the power
supply connection of the detector.
Error issuing control request to The USB connection between the detector and the Chromeleon server
FLD-3100@USB-1610103 may be interrupted. Check the USB connection. Check the power
supply connection of the detector.
Remove the detector specified in the message from the server
configuration or else, select a different detector from the list of
available detectors in the server configuration program.
Error reading from FLD-3100 Check the USB connection. The connection to the next hub must not
@USB-1610103 exceed 5 m. The overall connection length, including the hub
Data error (cyclic redundancy connections must not exceed 30 m.
check) Replace any defective USB cable or hub.
Error reading from FLD-3100 The USB connection between the detector and the Chromeleon server
@USB-1610103 may be interrupted. Check the USB connection.
The power supply to the detector may be interrupted. Check the power
supply connection of the detector.
Analysis run takes a The flow cell is still being Check the set flow cell temperature. At
long time to start or preheated. high flow rates, the flow cell may not
does not start at all. reach the desired temperature. Select a
lower temperature.
Strong noise, non- The eluent is dirty or their Use fresh eluent. Use fluorescence-
periodic baseline purity is insufficient. grade eluents only.
fluctuation/
the Raman S/N value The detector is defective. Contact Service.
cannot be met
The lamp is too old. Contact Service.
Incorrect signal parameters Also observe the guidelines for
were selected. optimizing the parameters (→ page 81).
Select suitable wavelengths
(→ page 78).
The flow cell is contaminated. Flush the flow cell (→ page 109).
The water is degraded. Use fluorescence-grade water.
Periodic baseline There are pressure fluctuations Purge the pump; check general function
fluctuation, pulsation from the pump. (→ Pump Manual).
There are air bubbles in the Purge the system.
system. (→ Pump Manual).
Peak tailing Too large extra column volume Use short capillary connections with a
suitable inner diameter.
There are bad capillary Use different capillaries, for example,
connections. Viper capillaries.
Flow cell input and output are Verify that the flow cell input and
exchanged. output are connected correctly.
Vertical lines in peak The detector had to Select a lower sensitivity. Check the
automatically adapt the Chromeleon Audit Trail to find out
Sensitivity. The peak is marked whether the Sensitivity was adjusted
by several lines. automatically.
Peak broadening, The inner diameter of the Change the capillary.
peak tailing, capillary to the detector is too
increased dead time large. Use different capillaries, for example,
There are bad capillary Viper capillaries.
connections.
Too large detector cell. The Use a smaller volume flow cell (micro
volume of the detector cell flow cell).
should not exceed the smallest
peak volume by more than
1/10.
The filter frits on the solvent Check the filter for permeability.
lines are clogged. Replace the filter frit if necessary
(→ Pump Manual).
Peak broadening, The capillaries are clogged, or Replace the capillaries. Use different
peak tailing, capillary connections bad. capillaries, for example, Viper
increased dead time capillaries.
(Cont'd)
The sample loop is clogged. Replace the needle (→ Autosampler
Manual).
The proportioning valve is Contact Service.
defective.
The column is overloaded or Clean or replace the column.
contaminated.
The solvent is degraded. Use fresh solvent.
Flow cell input and output are Verify that the flow cell input and
exchanged. output are connected correctly.
The selected response time is Select a suitable response time, e.g.,
too large. using the Chromeleon Program Wizard
(→ Fig. 31).
Reproducible ghost The degassing channels are Rinse the degassing channels
peaks in the contaminated. (→ Solvent Rack or Pump Manual).
chromatogram.
The solvents are degraded or Use fresh and appropriate solvents.
dirty or their purity is
insufficient.
Contamination occurs Flush the system with an appropriate
somewhere in the system. solvent.
Some broad ghost Late eluting peak from Extend the run time. Increase the elution
peaks in the previous analysis. strength of the gradient (higher organic
chromatogram. content). At the end of the run, flush
column with strong eluent.
Spikes There are air bubbles in the Check all fluid connections for
flow cell. tightness. Degas the mobile phase.
The detector lamp is old or not Contact Service.
properly installed.
Electrical interferences from Isolate the electrical circuit from strong
other instruments. current consumers. Consider using an
UPS (Uninterruptible Power Supply) to
filter current fluctuations.
The column temperature is Install a backpressure regulator at the
significantly above boiling flow cell outlet. Install a post-column
point of the mobile phase. cooler (→ TCC-3000RS Manual).
The flow cell temperature is Turn off the flow cell heating.
near the boiling point of the
mobile phase.
Negative peaks Sample solvent and mobile Dissolve the sample in the mobile phase.
phase differ in composition.
The fluorescence of the solute Select a different wavelength pair. Use a
is lower than the fluorescence mobile phase with less background
of mobile phase. fluorescence.
The fluorescence of the Consider using the negative peaks for
substance or eluent is quantification.
quenched by other
components.
Wrong polarization of the Check the analog output polarization.
analog output interface.
Wavelength The flow cell is incorrectly Verify that the flow cell is seated
verification fails. installed. correctly and that the screws are
tightened finger-tight.
The wavelength calibration is Perform a wavelength calibration
not within the acceptable (→ page 90).
range.
The flow cell is contaminated. Flush the flow cell (→ page 109).
The system does not meet the Observe the conditions on page 90. If
required conditions. the procedure is repeatedly interrupted,
contact Service.
Poor peak area The autosampler draws air There is not enough amount of sample
precision from the vial. in the vial, the needle height setting is
incorrect (→ Autosampler Manual), or
there are too many replicates.
There are air bubbles in the Flush the syringe (→ Autosampler
syringe or the autosampler Manual).
fluidics. Non-degassed wash liquid is used.
Degas the wash liquid (→ Autosampler
Manual).
There is an air bubble in the Perform a wash cycle (→ Autosampler
flow path. Manual).
The draw speed is too high. Reduce the draw speed (→ Autosampler
Manual).
The gas content of the sample Reduce the draw speed (→ Autosampler
is too high or saturated. Manual).
Degas the sample if possible.
The needle is clogged or the Replace the needle (→ Autosampler
needle tip is deformed. Manual).
The autosampler, the injection → Autosampler Manual
valve, or the syringe valve is
not tight.
Poor peak area Carry-over occurs in the Flush the needle using an appropriate
precision system. solvent (→ Autosampler Manual).
(Cont'd)
The capillary connections are Check and tighten the capillary
not installed properly or they connections.
are not tight. Exchange the needle seat if necessary
(→ Autosampler Manual).
Exchange the needle if necessary
(→ Autosampler Manual).
There are dead volumes in the Replace the fittings. Make sure that the
capillary connections. capillaries are installed correctly.
Thermo Fisher Scientific recommends
using Viper capillary connections
whenever possible.
The piston seals are not tight. Replace the seals (→ Pump Manual).
There is air in the working Purge the pump; check general function
head. (→ Pump Manual).
There is pump pulsation. Use degassed solvents.
The gradient is irreproducible. Change the gradient.
Check the pump function and degassing.
Check the filter frits in the solvent lines
for contamination and replace as
necessary.
The sample is unstable and Use new sample or change the
decomposes. conditions. Cool the sample in the
autosampler.
Baseline fluctuations see "Periodic baseline fluctuations,
pulsation"
The wrong emission Choose an emission wavelength which
wavelength was selected, e.g., is located near the apex of the spectrum.
in a UV spectrum flank. A wavelength switch might be required.
The selected response time is Select a suitable response time, e.g.,
too small. using the Chromeleon Program Wizard
(→ Fig. 31).
The environmental conditions Make sure that the temperature and air
are unstable. humidity are constant. Use column
thermostatting and/or flow cell
thermostatting. Avoid draft.
Contamination occurs Flush the system with an appropriate
somewhere in the system. solvent.
The detector had to Select an appropriate Sensitivity. Check
automatically adapt the the Chromeleon Audit Trail to find out
Sensitivity. whether the Sensitivity was adjusted
automatically.
7 Service
7.1 General Notes and Safety Precautions
The following sections describe all procedures for the detector that the user may perform.
All other maintenance and service procedures must be performed only by Thermo Fisher
Scientific service personnel.
Warning: The fluid components of the device may be filled with solvents that
are harmful to health. Wear appropriate personal protective
equipment. Rinse the fluid components with an appropriate solvent
to remove harmful substances.
For information about the proper handling of a particular substance
and for advice on specific hazards, refer to the material safety data
sheet for the substance you are using. Observe the guidelines of
Good Laboratory Practice (GLP).
7.2 Lamp
The lamp must be replaced only by Thermo Fisher Scientific Service for Dionex HPLC
Products. Never try to exchange the lamp or open the enclosure yourself.
You can monitor the lamp age. This function can help to decide when a lamp is due to be
replaced.
Lamp Age
Tip: You can extend the lifetime of the Xenon lamp to about four times the lifetime
compared to Standard mode by switching to LongLife mode. However, note
that sensitivity is roughly halved.
On the basis of the number of lamp flashes, Chromeleon calculates a value that indicates how
many hours the lamp was operated. The value is based on the assumption that the lamp was
operated in Standard mode. For the calculation of the expected lamp lifetime, one operating
hour is weighted depending on the selected lamp mode.
Example: If the lamp age in Chromeleon indicates 2000 hours, this means that the lamp
has reached about the half of its lifetime. Thus, if the lamp is operated in LongLife mode,
it is expected to operate for another 8000 hours.
Flush the flow cell when you suspect that eluent or sample components may have
deposited on the cell walls. Complete the following steps:
Warning: Flow cells can become extremely hot during operation. To avoid
possible injury, allow sufficient time for the flow cell to cool down
before replacing the cell.
Important: Make sure that you do not bend or damage the sensor.
4. Allow the sensor to adjust to the ambient temperature for a few minutes.
5. Turn on the detector.
6. If no error is reported after turning on the detector, operation can be resumed.
Tip: If the sensor is not dry, the Status LED remains red. If a message appeared on
the front panel display, select Clear on the navigation bar to remove the
message from the display.
Warning: Turn off the main power switch. Disconnect the power cord from its
source.
Fuse cartridge
Warning: Always install two new fuses. Use only the fuses indicated in
the following table.
To check which firmware version is installed in the detector and which version is included in
Chromeleon:
Tip: When updating the firmware via Chromeleon, this information will also be
provided during the download (see below).
Whenever a new firmware version is released for the detector, the new version will be
provided with the next Chromeleon Service Release and described in the related release
notes.
The new firmware will not be downloaded automatically to the detector when you install a
Chromeleon Service Release. To update the firmware in the detector, follow the steps below:
Important: To ensure that the download is successful, make sure that the
communication between the detector and Chromeleon is not
interrupted during the download and do not turn off the detector.
3. Right-click the detector in the timebase and select Properties on the menu.
4. On the General page (→ page 40), the firmware version provided by Chromeleon for
the detector is displayed in the Firmware field. If more than one firmware version is
available for the detector in Chromeleon, select the version from the Firmware list.
5. Click Download. A message displays the firmware version that is currently installed
in the detector and the version that will be downloaded from Chromeleon.
Tip: If the detector comes with a newer firmware than the version included in
Chromeleon, do not downgrade the firmware. Older firmware may be
incompatible with new hardware revisions.
6. Click Yes to start the download. (Click No to cancel the action.)
The download may take several minutes. The download is complete when Download
finished successfully appears in the Messages Server window in the Chromeleon Server
Configuration program. The message appears also in the Chromeleon Audit Trail.
If the download is not successful, the related messages appear in the Audit Trail. In this case,
turn off the detector. Turn on the detector again and repeat the download as described above.
If the download fails again, contact Service.
8 Technical Information
Specification FLD-3100 FLD-3400RS
Optical Design: Two monochromators with concave holographic gratings and
hyperbolic mirrors for highest efficiency in light transmission
Light source: Xenon flash lamp (15W);
Three different flash frequencies (HighPower, Standard, LongLife) can
be selected.
Reference system: Reference diode behind flow cell for compensation of lamp intensity
fluctuations
Data collection rate: Adjustable, max. 100 Hz Adjustable,
multi-channel: max. 4 Hz
single-channel:
max. 100 Hz (Chromeleon 6.80) or
200 Hz (Chromeleon 7.1 or later)
Spectra scanning modes: 2D scans: Excitation, Emission, Synchro
Under Chromeleon 7.1 or later:
3D scans: Excitation, Emission, Synchro
Wavelength range: Ex Min: 200 nm Ex Min: 200 nm
Ex Max: 630 nm Ex Max: 630 nm
(with Dual-PMT: 880 nm) (with Dual-PMT: 880 nm)
Em Min: 265 nm Em Min: 220 nm
Em Max: 650 nm Em Max: 650 nm
(with Dual-PMT: 900 nm) (with Dual-PMT: 900 nm)
Spectral bandwidth: Excitation: 20 nm
Emission: 20 nm
Programmable filter wheel: No (280 nm fixed) Yes, 5 positions (280 nm, 370 nm,
435 nm, 530 nm, Open)
Number of channels: 1 Up to 4
Excitation/emission wavelength < 250 ms
switching time:
Wavelength accuracy: ± 2 nm (over detector lifetime)
Wavelength repeatability: ± 0.2 nm
Sensitivity: Raman signal-to-noise ratio:
>550 ASTM over the over the entire lifetime of the lamp
(>2100 with dark current as reference)
Infrared option: A Dual-PMT Option for the near infrared region (up to 900 nm) may be
installed, without any loss in sensitivity in the UV spectral region.
Flow cell temperature control Ambient 15 °C to 50 °C
Analytical flow cell 6078.4230 For installation details, see page 48.
For details about the flow cell, see
page 117.
Micro flow cell 6078.4330 For installation details, see page 48.
For details about the flow cell, see
page 117.
Flow cell syringe injection/flushing kit 6078.4200 Kit with syringe and capillaries for direct
injection into a flow cell.
DAC board 6078.0305 Provides two analog outputs on the rear
panel. For installation information, refer to
page 34.
Drain system kit for UltiMate 3000 6040.0005 The kit includes all required components
systems and detailed installation instructions
Menu pen 6300.0100
Dual-PMT option Contact Upgrade kit for FLD detectors with a single
service. PMT. Installation must be performed by the
Thermo Fisher Scientific Service for
Dionex HPLC Products.
If the excitation monochromator of a fluorescence detector is set below the UV cutoff of the
mobile phase, the solvent will absorb some of the excitation light. Thus, the excitation
wavelength should always be above the UV cutoff of the solvent (recommendation: min.
30 nm).
The UV cutoff wavelengths of these solvents may differ from those predicted by Table 1.
Among other factors, the degassing quality and purity grade of the solvent affect the UV
cutoff. Therefore, the values listed below are approximate values only. The cutoffs listed in
the table apply to HPLC-grade solvents.
11 Index
SmartShutdown ............................................ 71
2 SmartStartup ................................................. 71
USB Driver ................................................... 37
2D Scans ............................................................ 74
Wavelength Calibration ................................ 91
2nd PMT ............................................................ 42
Wavelength Verification ............................... 91
Chromeleon Dialog
3
Detector ........................................................ 42
3D Scans ............................................................ 76 General ......................................................... 40
Signals .......................................................... 43
A Commands Dialog Box ..................................... 65
Configuration..................................................... 62
Accessories
Configurations ................................................... 19
Optional ...................................................... 120
Connection
Standard ...................................................... 119
Analog Output .............................................. 34
Analog Outputs .................................................. 23
Capillaries ..................................................... 46
Configure ...................................................... 36
Chromeleon Computer.................................. 32
Connect ......................................................... 35
Fluid .............................................................. 23
Installation..................................................... 34
Power Cord ................................................... 34
Autozero ............................................................ 89
USB .............................................................. 32
Consumables ................................................... 121
B
Control ............................................................... 26
Back ................................................................... 59 Automated .................................................... 67
Backpressure .................................................... 102 Chromeleon .................................................. 64
Baseline Behavior .............................................. 89 Direct ............................................................ 65
Baseline Noise ........................................... 77, 103 Control Panel ..................................................... 66
Baseline Spectrum ............................................. 74 Cutoff Filter ....................................................... 85
Batch .................................................................. 71 Cutoff Wavelengths ......................................... 123
C D
Cancel ................................................................ 60 DAC Board ...................................... 23, 34, 36, 42
Chromeleon........................................................ 64 Data Acquisition ................................................ 56
Automated Control ........................................ 67 Data Collection Rate.......................................... 86
Autozero........................................................ 89 DCMSLink ........................................................ 44
BaselineBehavior .......................................... 89 Detector (Dialog Box) ....................................... 42
Chromeleon 7 .......................................... 26, 76 Detector Configurations .................................... 19
Commands Dialog Box ................................. 65 Detector Display .......................................... 21, 55
Connect ......................................................... 64 Detector Sensitivity ........................................... 81
Control Panel ................................................ 66 Determine Wavelengths .................................... 78
Create Program ............................................. 70 Device View ...................................................... 70
Detector Configuration ................................. 40 Diagnostics ........................................................ 27
Detector Installation ...................................... 39 Diagnostics (Menu) ........................................... 63
Direct Control ............................................... 65 Dialog Box Commands ..................................... 65
Installation Program ...................................... 37 Disk Space ......................................................... 77
License .......................................................... 64 Display
Monitor System ............................................. 90 Brightness ..................................................... 72
Predictive Performance ................................. 92 Contrast ......................................................... 72
Program Wizard ............................................ 68 Menu Key ..................................................... 57
Server Configuration Program ................ 37, 39 Power-Up ...................................................... 55
Server Monitor ........................................ 37, 39 Drain Port .......................................................... 47
Set Wavelengths ............................................ 80 Drain System ..................................................... 47
Dual-PMT.......................................................... 19
E I
Emission Monochromator ................................. 17 Infrared Detector ............................................... 19
Emission Scan.................................................... 75 Installation
Emission Wavelength ........................................ 78 Connections .................................................. 32
Equilibration ...................................................... 51 In Chromeleon .............................................. 37
Equilibration (SmartStartup Wizard) ................. 51 In DCMSLink ............................................... 44
Equilibration Program ....................................... 51 Site ................................................................ 29
Error Messages .................................................. 98 System Setup ................................................ 31
Excitation Monochromator ................................ 16 Unpacking..................................................... 30
Excitation Scan .................................................. 74 Intended Use ...................................................... 12
Excitation Wavelength....................................... 78 Interior Components .......................................... 20
F L
Filter Wheel ....................................................... 85 Lamp ......................................................... 25, 108
Firmware Download .................................. 41, 115 Lamp Mode .................................................. 88
Firmware Update ............................................. 115 Replace ....................................................... 108
Firmware Version ............................................ 116 Lamp Age ........................................................ 108
FLD Type .......................................................... 42 Leak Detection .................................................. 72
Flow Cell ................................................... 53, 109 Leak Sensor ......................................... 25, 72, 113
Flush ........................................................... 109 Leak Sensor Mode ....................................... 62, 72
General .......................................................... 24 Lifetime (Lamp) .............................................. 108
Install ............................................................ 48 Limit of Detection ............................................. 77
Notes ............................................................. 53
Remove ....................................................... 111 M
Replace........................................................ 110
Main (Menu) ..................................................... 61
Volume.......................................................... 24
Maintenance ...................................................... 95
Flow Cell Temperature ................................ 88, 92
Maintenance Intervals ....................................... 95
Flow Cell Types................................................. 24
MaxPMTSaturation ........................................... 82
Fluid Connections .............................................. 23
Menu ................................................................. 58
Fluorescence ...................................................... 16
Configuration ................................................ 62
Fluorescence Intensity ....................................... 77
Diagnostics ................................................... 63
Found New Hardware Wizard ........................... 38
Layout ........................................................... 59
Front Panel Elements ......................................... 21
Main.............................................................. 61
Function Key
Overview ...................................................... 58
Arrow Down ................................................. 59
Service .......................................................... 63
Arrow Up ...................................................... 59
Show ............................................................. 57
Back .............................................................. 59
Menu Key .......................................................... 57
Cancel ........................................................... 60
Messages ........................................................... 98
Clear ........................................................ 60, 98
Method Development ........................................ 78
Next......................................................... 60, 98
Mobile Phase ............................................. 52, 123
Ok ................................................................. 60
Module Address ................................................ 41
Prev ......................................................... 60, 98
Multi-Channel Mode ......................................... 73
Select............................................................. 59
Multi-Channel Performance .............................. 87
Toggle ........................................................... 60
Multiple Wavelength ................................... 73, 87
Fuse Cartridge.................................................... 22
Fuse Replacement ............................................ 114
N
G Negative Peaks ................................................ 105
Noise ......................................................... 77, 103
General (Dialog Box) ........................................ 40
Not Calibrated Message .................................... 90
Ghost Peaks ..................................................... 104
U W
Unit Description Wavelength Calibration ..................................... 90
Flow Cells ..................................................... 24 Wavelength Verification ................................... 90
Overview....................................................... 15 Fails ............................................................ 105
Unpacking.......................................................... 30 Steps to Perform ........................................... 91
USB ................................................................... 32 Wellness ............................................................ 27
USB Configuration File ..................................... 38
USB Port ............................................................ 23 Z
UV Cutoff ........................................................ 123
Zero Order Mode ............................................... 74
V
Viper Capillaries ................................................ 46
Virtual Mode...................................................... 40