Alligent
Alligent
MassHunter Workstation
Quick Start Guide
This guide describes how to use the Agilent 7700 Series ICP- MS
MassHunter Workstation.
Agilent Technologies
Startup 3
Preparing for Analysis 4
Things to check before analysis 4
Prepare tuning solutions 4
Ignite the plasma 5
Check tuning 6
Setting Quantitative Method Parameters 12
Set up a Quantitative Method 12
Access Method parameters directly 19
Use the Method Wizard to create a method 19
Running the Samples 21
Set up the Sequence 21
Analyze the samples 23
Quantitative Data Analysis 25
Typical scenarios for Data Analysis 25
Open an existing batch for data analysis 26
Creating a new batch for data acquisition 26
Create the Data Analysis (DA) method for Quantitative data analysis 28
Process the batch 32
View analysis results 33
Save analysis results 34
Generate a report 34
Semi-Quantitative Analysis 35
Prepare for SemiQuant Analysis 35
Create a SemiQuant acquisition method 35
Analyze the samples 37
Create a new batch or open a new batch for SQ data analysis 37
Create the Data Analysis (DA) method for Quantitative data analysis 28
Process the batch 40
Correcting the Semiquant Factors 41
Change the SemiQuant Factors 42
Toolbar The following shortcuts are available on the ICP- MS MassHunter Workstation
toolbar:
Utilities
• Argon gas pressure: 500 to 700 kPa
• Cell gas (Helium): 90 to 130 kPa
• Cell gas (Hydrogen): 20 to 60 kPa
• Exhaust duct (on)
• Cooling water (Chiller or heat exchanger on)
• Drain and rinse tank (not full)
2 Confirm that the instrument is in Standby mode by checking the title bar of
the Instrument Control panel.
3 Ignite the plasma by clicking the Ignite Plasma icon in the toolbar.
4 Once the plasma is on and the instrument goes from standby to analysis
mode, check tuning as described in the following section.
Detector
AMFC Turbo-
Molecular
Pump
Open the Tuning panel by selecting Tune from the Instrument menu,
or by clicking the Tune icon on the ICP- Top toolbar.
Select Mode & start Autotune Set Acquisition parameters for tuning
Tip See the “Tuning 7700” in online help for more information on individual
tuning parameters.
Plasma Correction
Execution of plasma correction is necessary in the following cases:
• When the instrument is installed
• When the nebulizer has been changed
(However, if the same nebulizer unit is reused repeatedly by detaching and
reattaching, it is not necessary to conduct the correction each time as long
as the nebulizer is installed correctly.)
• When the sampling cone is changed
• When the torch is changed
• When the matrix tolerance has changed after the instrument has been used
for 6- 12 months and normal maintenance procedures have been followed
Once plasma correction is performed, there is no need to conduct it again in
most cases, provided the instrument is used for normal measurement.
2 If the desired sensitivity is not achieved, select Autotune from Tume menu.
Refer to the Help and execute Autotune.
3 After completing autotune, check the sensitivity parameters on the ICP- MS
Tuning - Sensitivity window.
4 Save the tune file by selecting Save from the File menu. In general you will
want to overwrite the tune file that was open, so that it has the updated
values.
5 (optional) Generate a tune report by selecting Generate Report from the
File menu. Enter optional comments if desired and click OK. A report
showing the following information is sent to your printer:
• Sensitivity data
• Resolution/Axis data
• Lens parameter settings
Depending on how your system is configured, tuning results will also be
recorded in the maintenance log.
Tip You can also get a hard copy of current tune parameters by clicking the
Stop button and selecting Print from the File menu.
Parameter No Gas Mode Cell Gas Mode High Energy Collision Mode *2
Recommended Recommended Recommended Recommended Recommended Recommended
Value Range Value Range Value Range
RF Power [W] 1550 Fixed 1550 Fixed 1550 Fixed
Smpl Depth [mm] 8.0 Fixed 8.0 Fixed 8.0 Fixed
Carrier Gas [L/min] 1.05 1.01 to 1.11 1.05 1.01 to 1.11 1.05 1.01 to 1.11
Makeup Gas [L/min] 0 0 to 1.11 0 0 to 1.11 0 0 to 1.11
Dilution Gas [L/min] 0 Fixed 0 Fixed 0 Fixed
Neb Pump [rps] 0.1 Fixed 0.1 Fixed 0.1 Fixed
S/C Temp [degC] 2 Fixed 2 Fixed 2 Fixed
He or H2 gas [ml/min] 0 Fixed 3.6 (He) 3.2 to 4.0 (He) 10 (He) 7 to 10 (He)
4.0 (H2) 3.6 to 4.4 (H2)
Extract 1 [V] 0 Fixed 0 Fixed 0 Fixed
Extract 2 [V] -180 -200 to -160 -180 -200 to -160 -180 -200 to -160
Omega Bias [V] -80 -110 to -70 -80 -110 to -70 -80 -110 to -70
Omega Lens [V] 10 7 to 12 10 7 to 12 10 7 to 12
Cell Entrance [V] -30 -40 to -30 -40 -40 to -30 -130 -150 to -110
Cell Exit [V] -50 -60 to -40 -60 -60 to -40 -150 Fixed
Deflect [V] 10 8 to 15 0 -5 to 4 -80 -90 to-70
Plate Bias [V] -40 -50 to -30 -60 Fixed -150 Fixed
OctP RF [V] 180 150 to 200 180 150 to 200 190 180 to 200
*1
OctP Bias [V] -8 -10 to -6 -18 Fixed -100 Fixed
*1
QP Bias [V] -3 -7 to -3 -15 Fixed -96 -97 to -90
Parameter High Sensitivity Cell Gas Mode High Energy Collision Cool Plasma
Mode*2
Recom- Recom- Recom- Recom- Recom- Recom- Recom- Recom-
mended mended mended mended mended mended mended mended
Value Range Value Range Value Range Value Range
RF Power [W] 1500 fixed 1500 fixed 1500 fixed 600 fixed
Smpl Depth [mm] 8 7 to 10 8 7 to 10 8 7 to 10 18 fixed
Carrier Gas [L/min] 0.7 fixed 0.7 fixed 0.7 fixed 0.7 fixed
Makeup Gas [L/min] 0.5 0.3 to 0.7 0.5 0.3 to 0.7 0.5 0.3 to 0.7 0.75 0.6 to 1.2
Dilution Gas [L/min] 0 fixed 0 fixed 0 fixed 0 fixed
Neb Pump [rps] 0.1 fixed 0.1 fixed 0.1 fixed 0.1 fixed
S/C Temp [degC] 2 fixed 2 fixed 2 fixed 2 fixed
He or H2 gas [ml/min] 0 fixed 3.6(He) 3.2 to 4.0(He) 10(He) 7 to 10(He) 0 fixed
4.0(H2) 3.6 to 4.4(H2)
Extract 1 [V] 4.5 3 to 7 4.5 3 to 7 4.5 3 to 7 -120 -200 to -40
Extract 2 [V] -100 -170 to -60 -100 -170 to -60 -100 -170 to -60 -5 -30 to 5
Omega Bias [V] -70 -100 to -30 -70 -100 to -30 -70 -100 to -30 -70 -120 to -30
Omega Lens [V] 11 5 to 15 11 5 to 15 11 5 to 15 6 3 to 10
Cell Entrance [V] -30 -40 to -30 -40 -40 to -30 -130 -150 to -110 -30 -40 to -30
Cell Exit [V] -50 -60 to -40 -60 -60 to -40 -150 fixed -60 fixed
Deflect [V] 12 8 to 15 0 -5 to 4 -80 -90 to -70 9 5 to 13
Plate Bias [V] -40 -50 to -30 -60 fixed -150 fixed -60 fixed
OctP RF [V] 180 150 to 200 180 150 to 200 -190 180 to 200 150 100 to 200
OctP Bias [V] *1 -8 -12 to -6 -18 fixed -100 fixed -18 -30 to -10
QP Bias [V] *1 -3 -5 to -3 -15 fixed -96 -97 to -90 -5 -5 to -3
7a
9b
9a
9c
d Repeat for each mass in the table. For masses such as 71 that are
monitored in both steps, remember to enter integration times for both.
10b
10a
c Mark the Return to First Tune Step option at the bottom of the screen,
and click OK.
10c
11 On the Peristaltic Pump Program dialog box, set the following parameters,
then click OK. See online help for more information on these parameters
and on the optional features: Intelligent Rinse and Execute Pre- emptive
Rinse.
• Before Acquisition
• After Acquisition (Rinse Port)
• After Acquisition (Rinse Vial)
12 (optional) Set up pre- emptive rinsing as follows:
a Select Set PeriPump Program from the PeriPump menu in the
Acquisition window.
b On the Peristaltic Pump Program dialog box, mark the Execute
Pre- emptive Rinse option at the bottom of the screen.
c Enter an initial time of 15 seconds, then click OK.
d Adjust the time so that the analysis is completed 5 seconds before the
rinse solution reaches the nebulizer.
13 To save the method:
a On the Method Save Options dialog box, mark all items, and click OK.
b On the Save Method As dialog box, enter a method name, and click OK.
For high-concentration Na, Mg, K, and Ca, it is safer to prepare their mixed standard
solutions separately instead of mixing with the SPEX mixed standard solution, so as to
prevent contamination with the reagent, particularly if the required concentration level is
1/100 of the standard.
If you wish, you can type in a different directory name instead. The name
can be up to eight characters long. The batch folder will be created in
C:\ICPMH\1\DATA\.
5 (optional) Select the Import DA Method from Existing Batch check box to
import an existing data analysis method from the specified data batch
directory. You can import the DA Method Only or the DA method and Std.
Data.
6 Click the Edit DA Method button in the lower left of the dialog box, then
create a Data Analysis method as described on page 28.
7 Click the Run Sequence button to start the run. The Run Sequence Status
dialog box appears.
Description
To import an existing The data was acquired with reference to a Data Analysis (DA) method.
method (E.g. the “Edit DA Method” button was clicked or the “Import DA Method from Existing Batch”
option was selected when setting up the sequence).
In this scenario, the ICP-MS Data Analysis window opens automatically after acquiring the data.
Proceed in one of the following ways:
• If no changes are required to the DA method, then proceed to “View analysis results” on
page 33 and to “Generate a report” on page 34.
• If you wish to modify the existing DA method for this acquired data, then proceed to “Create
the Data Analysis (DA) method for Quantitative data analysis” on page 28 to open the Method
Editor and make changes to the DA method.
To create a method You want to create a DA method without reference to any acquired data.
before performing data a Follow the steps in“Open an existing batch for data analysis” on page 26 to create a new batch
acquisition folder, since a data batch does not already exist.
b If desired, import samples as described in Step 3.
c Proceed to “Create the Data Analysis (DA) method for Quantitative data analysis” on page 28.
2 Select Data Analysis Method from Method Tasks section 2 (on the left side
of the screen) to display the Data Analysis Method pane
3 Set the options as follows:
a Mark the check box for FullQuant Analysis.
b Set the Analysis Mode to Spectrum.
c Select the correction method from the Interference Correction list.
3a
3b
3c
As a new file: Select Save Analysis File As from the File menu.
Generate a report
1 Select Generate from the Report menu in the MassHunter ICP- MS Analysis
window.
2 Mark the desired report options and click OK (see example below).
3 On the Method Information dialog box, set the following parameters, then
click OK:
a Enter a comment
b Be sure that the Data Analysis check box is checked; this is required to
run the data analysis automatically after data acquisition.
The same scenarios apply for offline Semi-quantitative data analysis as described in
NOTE “Typical scenarios for Data Analysis” on page 25.
2 Select Data Analysis Method from Method Tasks section 2 (on the left side
of the screen) to display the Data Analysis Method pane.
3 Set the options as shown below:
a Mark the check box for SemiQuant Analysis.
b Set the Analysis Mode to Spectrum.
c Select the correction method from the Interference Correction list.
3a
3b
3c
6a
In this Book
This Quick Start Guide
presents first steps to
using the Agilent 7700
Series ICP- MS MassHunter
Workstation.
*G7200-90210*
G7200-90210
Agilent Technologies