VGB S 116-00-2016 04 en Preservation of Power Plant (LICENSE VGB OM)
VGB S 116-00-2016 04 en Preservation of Power Plant (LICENSE VGB OM)
Preservation of
Power Plants
VGB-S-116-00-2016-04-EN
(formerly VGB-R 116)
Publisher:
VGB PowerTech e.V.
Publishing house:
VGB PowerTech Service GmbH
Verlag technisch-wissenschaftlicher Schriften
Deilbachtal 173, 45257 Essen, Germany
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The term “work” covers the publication at hand as printed hard copy and as digital-
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Disclaimer
VGB-Standards are recommendations, the application of which is optional. VGB-
Standards represent the state of the art at the time of publication. No claim regarding
its completeness and correctness is made as a matter of principle.
Application of VGB-Standards is carried out at the user's own responsibility and risk.
VGB PowerTech accepts no legal liability in the event of any claim relating to or re-
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Authors
The following companies and associations participated in the establishment of this
standard:
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Representatives of VGB-Offices:
Hartwig VGB PowerTech e.V., Essen
Heiting, Dr. VGB PowerTech e.V., Essen
Wecker, Dr. VGB PowerTech e.V., Essen
Stolzenberger VGB PowerTech e.V., Essen
With this standard the authors hope to have made a major contribution to an
increased efficiency regarding the preservation of power plants.
Our thanks are due to all participants for their careful and thorough work which has
gone into the making of this guideline during numerous committee meetings.
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With this guideline the authors hope to have made a major contribution to the preser-
vation of power plants.
Our thanks are due to all participants for their careful and thorough work which has
gone into the making of this guideline during numerous committee meetings.
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Table of contents
1 Scope and introduction .......................................................................... 13
1.1 Scope ....................................................................................................... 13
1.2 Introduction ............................................................................................... 13
2 Fundamentals of off-line corrosion....................................................... 16
3 Fundamentals of preservation............................................................... 24
3.1 General ..................................................................................................... 24
4 Materials .................................................................................................. 25
4.1 Material surfaces ...................................................................................... 25
4.2 Material surfaces ...................................................................................... 26
5 Preservation methods for the water/steam side .................................. 29
5.1 Wet preservation....................................................................................... 31
5.2 Dry preservation ....................................................................................... 32
5.3 Inert gas blanketing (inerting) ................................................................... 34
5.4 Preservation with volatile corrosion inhibitors (VCI) .................................. 35
5.5 Preservation with filming amines .............................................................. 36
5.6 Oils, waxes and fat ................................................................................... 37
5.7 Temporary coating .................................................................................... 39
6 Plant value conservation and test plans for preservation .................. 40
6.1 Wet preservation....................................................................................... 41
6.2 Dry preservation ....................................................................................... 42
6.3 Inert gas blanketing (inerting) ................................................................... 43
6.4 Volatile corrosion inhibition ....................................................................... 43
6.5 Filming amines.......................................................................................... 43
7 Preservation of power plant components upon fabrication, during ......
transportation, and storage on plant site or in the power plant ......... 45
7.1 Specific requirements ............................................................................... 45
7.2 Preservation requirements ........................................................................ 46
7.3 Acceptance of preservation ...................................................................... 46
7.4 Removal of preservatives ......................................................................... 47
8 Storage classes and conditions ............................................................ 50
8.1 General ..................................................................................................... 50
8.2 Storage classes ........................................................................................ 50
8.2.1 Class A ..................................................................................................... 51
8.2.2 Class B ..................................................................................................... 51
8.2.3 Class C ..................................................................................................... 51
8.2.4 Class D ..................................................................................................... 52
8.2.5 Class E ..................................................................................................... 52
8.3 Storage categories.................................................................................... 52
8.3.1 Storage category 1: Fully air-conditioned storage room ........................... 52
8.3.2 Storage category 2: Closed (air-conditioned) storage room ..................... 53
8.3.3 Storage category 3: Covered storage area ............................................... 53
8.3.4 Storage category 4: Open storage area, material covered ....................... 53
8.3.5 Storage category 5: Open storage area.................................................... 53
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11.4 Flocculation plants and cooling tower make-up water plants .................... 81
11.4.1 Preservation methods in case of outage with permanent start-up ................
readiness .................................................................................................. 81
11.4.2 Preservation methods in case of extended outage without start-up..............
readiness .................................................................................................. 82
11.4.3 Filter units ................................................................................................. 82
11.4.3.1 Filter chamber press ................................................................................. 82
11.5 Cooling towers .......................................................................................... 83
11.5.1 Natural-draught cooling tower ................................................................... 83
11.5.2 Natural-draught cooling tower used in combination as flue-gas stack ...... 84
11.5.3 Mechanical-draught cooling tower/hybrid cooling tower ........................... 84
11.5.4 Dry cooling towers .................................................................................... 84
12 Preservation of components in water treatment systems .................. 85
12.1 Gravel filters/multi-media filters................................................................. 85
12.2 Ion exchanger units .................................................................................. 85
12.2.1 Cation exchanger resins (H and Na exchange resins).............................. 86
12.2.2 Anion exchangers ..................................................................................... 86
12.2.3 Mixed-bed unit .......................................................................................... 87
12.3 Membrane systems .................................................................................. 88
12.3.1 Reverse osmosis (RO) systems shutdown and lay-up consideration ....... 88
12.3.2 Ultra- and micro-filtration .......................................................................... 90
12.3.3 Membrane degasification ..........................................................................90
12.4 Electro-deionisation .................................................................................. 90
13 Fuel supply system ................................................................................ 91
13.1 Coal firing system ..................................................................................... 91
13.1.1 Coal handling system ............................................................................... 91
13.1.2 Coal bins and bunkers .............................................................................. 91
13.1.3 Feeders .................................................................................................... 92
13.1.4 Pulverising mills ........................................................................................ 92
13.2 Fuel supply lines ....................................................................................... 93
13.2.1 Pulverised-fuel supply line ........................................................................ 93
13.2.2 Oil supply lines.......................................................................................... 93
13.2.3 Booster pumps.......................................................................................... 93
13.2.4 Gas supply lines ....................................................................................... 94
13.3 Burners, firing systems ............................................................................. 94
13.3.1 Pulverised-fuel burners ............................................................................. 94
13.3.2 Oil burners ................................................................................................ 94
13.3.3 Gas burners .............................................................................................. 94
14 Air supply system ................................................................................... 95
14.1 External/internal combustion air intake ..................................................... 95
14.2 Steam air heater ....................................................................................... 95
14.3 Regenerative air heaters .......................................................................... 95
14.4 Forced-draught fans/primary air fans ........................................................ 97
14.5 Forced-draught intake ducts ..................................................................... 97
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15 Flue-gas system...................................................................................... 98
15.1 Combustion chamber, convective heating surfaces and 2nd pass ...............
or blank pass ............................................................................................ 98
15.2 Furnace bottom ash removal .................................................................... 98
15.3 Flue-gas recirculation ............................................................................... 99
15.4 Flue-gas ducts including dampers upstream of electrostatic ........................
precipitator ................................................................................................ 99
16 Flue-gas side preservation of steam generators ............................... 100
16.1 Preservation methods ............................................................................. 102
16.1.1 Thermal methods .................................................................................... 102
16.1.2 Dry air method ........................................................................................ 103
16.1.3 Blast cleaning and preservation with alkalised pressurized water .......... 105
16.1.4 Chemical methods .................................................................................. 105
16.2 Flue-gas side preservation of coal-fired steam generators ..................... 106
16.3 Flue-gas side preservation of oil-fired steam generators ........................ 106
16.4 Flue-gas side preservation of steam generators fired with ...........................
substitute fuels ........................................................................................ 108
16.5 Flue-gas side preservation of waste-heat recovery boilers ..................... 108
17 Flue-gas cleaning systems .................................................................. 111
17.1 NOx reduction systems ........................................................................... 111
17.1.1 High-dust catalyst ................................................................................... 111
17.1.2 Tail-end catalyst...................................................................................... 112
17.1.3 Ancillary DeNOx systems ....................................................................... 112
17.1.3.1 Storage of ammonium hydroxide ............................................................ 112
17.1.3.2 Storage of pressure-liquified ammonia ................................................... 113
17.2 Electrostatic precipitator (ESP) ............................................................... 114
17.2.1 Electrostatic precipitator casing with electrodes and rapping system, ..........
insulators ................................................................................................ 114
17.3 ESP ancillary systems ............................................................................ 114
17.3.1 High-voltage units ................................................................................... 114
17.3.2 Ash disposal ........................................................................................... 114
17.4 Fabric filter .............................................................................................. 115
17.5 Fabric filter ancillary systems .................................................................. 115
17.5.1 Cleaning system/compressed-air supply ................................................ 115
17.5.2 Ash disposal ........................................................................................... 115
17.6 Flue-gas desulphurisation system (FGD) ............................................... 115
17.6.1 Absorber inlet ......................................................................................... 115
17.6.2 Absorber with spray bank and mist eliminator ........................................ 116
17.7 FGD ancillary systems ............................................................................ 117
17.7.1 Absorber circulation pumps (large pumps) ............................................. 117
17.7.2 Suspension pumps (e.g. gypsum discharge pump) ................................ 118
17.7.3 Pumps, general requirements ................................................................. 118
17.7.4 Pipework and valves ............................................................................... 119
17.7.5 Compressors .......................................................................................... 119
17.7.6 Agitators ................................................................................................. 119
17.7.7 Measuring equipment ............................................................................. 120
17.7.8 Gypsum drainage systems ..................................................................... 120
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1.1 Scope
This VGB Standard shall apply to:
plants for firing fossil fuels
plants for firing substitute fuels
This standard comprises all essential process systems which are to be consid-
ered during plant outage or shutdown and have to be preserved.
This standard neither explicitly deals with electrical systems nor instrumentation
and control equipment. Nevertheless, such systems require that adequate
measures be taken during long outages (e.g. standstill during summer or cold
reserve) so that the functionability of such systems and equipment is maintained.
To this end, specialists shall be involved prior to taking preservation measures
and the respective measures shall be included in the specific plant preservation
plan.
1.2 Introduction
Meanwhile, the preservation subject has become a question of major importance for
plant owners/users and component manufacturers.
Due to:
long transportation routes (among others, world-wide manufacturing of compo-
nents by international manufacturers),
intermediate and long-time storage in the case of new plant projects,
extended revision periods (among others, due to long operational periods) and
changed requirements (among others due to the “Energiewende”)
the requirements regarding type and extent of preservation measures have in-
creased.
Prevention of damage is only possible in case of early determination, detailed plan-
ning, implementation, and regular control of the respective measures.
Where new power plants are built or existing power plants are taken out of operation
(short and long outage periods) measures shall especially be taken to protect the
power plant from off-line corrosion and further plant-specific measures shall be tak-
en to avoid consequential damage.
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The corrosion of steam turbine blades or compressors in gas turbines may e.g. lead
to considerable efficiency losses and thus to high economic losses. Example: Blade
surface roughness with a centre-line average height from 5µm changing to 20 µm
will lead to an efficiency loss of 0.7 %. For a 550 MW turbine this results in a loss of
3.85 MW (Source: EPRI).
These measures and recommendations principally apply to all plants independent-
ly of plant size or individual design.
Preservation (or lay-up) measures principally are intended to counteract off-line cor-
rosion which is favoured by:
humid air
condensation water
oxygen-containing water
salt-containing water
chloride-containing water
acid-reacting layers
hygroscopic layers
When selecting the appropriate preservation method, a variety of prerequisites and
conditions must be considered which are covered by this guideline.
Depending on outage periods specific measures shall additionally be taken to
protect components and systems against impairments and damage (e.g. lubricating
oil systems, rotating equipment, water treatment systems, etc.) which are not com-
pulsorily attributable to corrosion (e.g. microbiological fouling in water treatment
systems, in lubricating oil systems, damage on valve seats or on rotating equipment,
and the like).
A principal and decisive aspect for successful preservation is always subject to
complete consideration of all systems and components as well as of intersections
between sectional preservation measures and methods and consequently the result-
ing detailed planning and the required monitoring of such measures and methods.
The most critical power plant components (ordered to the exent of damage) with
regard of component failure due to corrosion are:
boiler and boiler components
turbines
cooling systems
other power plant components
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When handling the respective chemicals, the pertinent national workplace and
environmental protection regulations shall principally be observed. In Germany these
are, e.g. the Ordinance on Hazardous Substances, Classification and Labelling of
Chemicals (GHS) Regulation, European Classification, Labelling and Packaging of
Substances and Mixtures (CLP) Regulation, the Biocides Regulation, and many
others.
Where, upon consumption, the chemicals or residual matter have to be disposed off,
the local waste water/effluent disposal regulations as well as operating licences shall
be observed.
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The electrolyte content means all ions contained in the water which originate from
dissolved salts, alkalising agents or acids, e.g. silica. The electrolyte content can be
roughly determined by means of conductivity measurements.
The electrochemical reaction can be examined on a half cell (this is a piece of metal
immersed in an electrolyte bath). Between the metal and the metal ions the following
interactive reactions occur at the electrolyte/metal interface:
anodic reaction: Me → Men+ + n e-
cathodic reaction: Men+ + n e- → Me
The decisive process initiating corrosion is the electrolytic dissolution of the metal at
the electrolyte/metal interface. The positively charged ions leave the metal whereas
the corresponding number of electrons remains in the metal until reaching a state of
equilibrium.
Two metals joined to each other to be conductive or areas of one metal with differing
potential will form a corrosion element when wetted with an electrolyte. Due to the
balance of charge via the electrically conductive connection and the electrolyte no
state of equilibrium can be obtained at the two electrodes. The less noble electrode
then becomes the anode, the nobler electrode becomes the cathode. The strong an-
odic reaction (Me → Men+ + n e-) gradually leads to the metal’s dissolution (oxida-
tion), i.e. the metal oxidises to form metal ions. The electrons then released flow
though the electric conductor to the cathode and are consumed for cathodic reaction
(reduction). The oxidation at the anode and the possibility of reduction at the cathode
are closely interrelated which also favours the corrosion rate.
The most important reduction reactions are the hydrogen reduction (as of pH < 5) =
hydrogen corrosion, the oxygen reduction = oxygen corrosion and the reduction of
metal ions, with the latter being of little importance to power plants.
In the following some factors influencing corrosion are mentioned:
pH value:
Iron behaves relatively stable in alkaline solutions because protective cover layers
can be formed. At pH values of less than 7, however, there will be a strong corro-
sive attack.
However, in the case of copper alloys a pH value exceeding 9.3 shall be avoided.
Where aluminium alloys are present, an increase of the pH value for the purpose
of preservation is not possible. Usually, aluminium alloys are not subject to corro-
sive attack in a narrow range of pH values between 6.5 and 8.5.
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Oxygen content:
The corrosion rate in oxygen-rich aqueous solutions is very low since the cathodic
reaction (2 H2O + 2 e- → H2 + 2 OH-) is very slow.
Temperature:
With the increase of temperature chemical reactions and thus corrosion rates will
be accelerated.
Ion concentration and type:
Especially chloride and/or sulphate ions, but also other ionic impurities will increase
the corrosion effect, e.g. where deposits, contaminants and/or ionic impurities (e.g.
cooling water leakage) in the water are present (increased conductivity), the risk of
off-line corrosion will increase.
Passive corrosion protection comprises all measures taken to prevent electrolyte
contact with the metal.
Among the types of corrosion without mechanical loading is the uniform corrosion
which considerably contributes to the iron load during plant re-starts thus causing
consequential damage (deposits, erosion, overheating, etc.), especially during fre-
quent start-up processes.
Great danger potential is caused by those types of corrosion that are based on the
formation of local corrosion elements. Locally limited corrosion is considerably more
dangerous and, as a rule, cannot be detected prior to the occurrence of damage.
The types of corrosion mentioned here do not compulsorily represent a complete list
of all operational impairments/damage, but as experience has shown most frequently
occur.
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Pitting corrosion:
This type of locally confined corrosion is due to increased electrolyte concentration
(e.g. chlorides) causing crater-shaped undercutting or pinhead type pits on materials
covered with porous or damaged corrosion-inhibiting passive layers.
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Crevice corrosion:
This type of corrosion occurs at narrow gaps or clearances (e.g. tube expansions,
threads). The driving force is the difference in potential (differences in concentration)
of the substances causing corrosion. The natural concentration difference of oxygen
on the outside (high concentration) to the interior in the gap (low concentration) will
already suffice. Impurities that may have concentrated in the gap due to capillary
action will often intensify this effect.
Due to their design nearly all components in
the water/steam circuit show crevices
= > Immanent risk of crevice corrosion
Selective corrosion:
Under the influence of a corrosive medium individual alloying elements are dissolved
from the structure, and the final condition will be a porous spongy metal structure
consisting of non-dissolvable alloying elements. Selective corrosion may e.g. occur
on copper-zinc or copper-nickel-alloys (cf. VGB-R 106).
Acid corrosion:
When subjected to an acid, the metal will be dissolved directly and very quickly due
to the acid ambient conditions (pH value < 7, e.g. by CO2).
Microbiologically induced corrosion:
Microbiologically induced corrosion (MIC) will occur in power plants only during out-
ages or in stagnant operational sections. To initiate MIC, microbial contamination of
the respective system with bacterial strain is required. Corrosion will be initiated and
favoured by often acid metabolites. The most well-known bacterial strain causing
MIC are sulphate-reducing bacteria, iron and manganese bacteria.
MIC may not only occur in water-bearing systems, but also in oil-bearing systems.
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3 Fundamentals of preservation
3.1 General
Water/steam carrying as well as flue-gas side power plant components will be sub-
jected to corrosion during plant outages. Corrosion during outage periods may occur
in the aqueous phase if oxygen or salts and acids are present (e.g. CO2 due to in-
gress of air). This locally occurring type of corrosion called pitting corrosion will par-
ticularly endanger plant parts).
Tube material
Oxygen corrosion. No protective function due to exfoliated structure of magnetite layer (active
condition)
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4 Materials
All commonly used ferritic boiler materials including martensitic materials may be
subject to the above mentioned corrosion processes. The materials primarily used
in steam generator construction can be taken from VGB Standard VGB-S-513.
Austenitic materials are corrosion-resistant in the event of most of the corrosion-
enhancing factors mentioned above. An exception to this rule is the presence of chlo-
ride ions especially at locations where these ions can accumulate due to evaporation
of water.
Other materials used for power plant components, e.g. copper or aluminium based
alloys are prone to off-line corrosion.
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Corrosion rate
0 50 100
relative humidity in %
Source: W. H. J. Vernon, A laboratory study of the atmospheric corrosion of metals. Part II.—Iron: the primary
oxide film. Part III.—The secondary product or rust (influence of sulphur dioxide, carbon dioxide, and suspended
particles on the rusting of iron), Transactions of the Faraday Society, vol. 31, 1935, pages 1668 – 1700, The Roy-
al Society of Chemistry.
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Starting with a relative humidity of approx. < 50 % the corrosion rates will attain such
low values that the beginning of corrosion protection can be assumed.
In practice, however, a relative humidity of < 40 % should be attained to safely obtain
and maintain system corrosion protection over the entire preservation period.
Where corrosive contaminations are present (e.g. SOx, or sea water atmospheres,
etc.) the corrosion rate will increase correspondingly. Then a relative humidity < 30 %
is recommended.
The Vernon diagram correctly describes the dependence of corrosion on relative
humidity, however in practice the absolute humidity shall be reduced in the respec-
tive systems such that the relative humidity safely remains below the critical limit irre-
spective of any possible temperature variations.
The exclusive reduction of the relative humidity without sufficient dehumidification is
technically possible and may be applied, under certain circumstances, over outage
periods strictly limited in time, however is principally not recommended since the risk
of local sub-dew point temperatures cannot be safely excluded.
Further details on the individual processes are described in the chapters to follow.
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Shutdown of boiler
Maintain overpressure
Preservation with steam or
Without draining With draining N2 cushion
Dry preservation
Preservation with
operational fluid
Inspection/repairs
Filling/Pressure testing
Yes Yes
Repair required? Repair required?
No No
Wet preservation
Operation
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The following items shall principally be considered when selecting the preservation
method:
duration and frequency of outage,
maximum time available for starting-up the plant again,
handling and technical expenditure,
secondary effects on plant components,
disposal of preservation means,
economic efficiency,
frost hazard,
safety at workplace and environmental protection,
effects on re-start/operation.
Remarks on the use of chemicals
o Where chemicals are used, all pertinent safety and water conservation
rules and regulations shall be observed.
o When the plant is re-started it shall be taken into account that preservation
solutions not meeting the requirements for permanent operation have to be
disposed off in total or in part upon finalisation of outage. Too high ammo-
nia concentrations in the start-up condensate will endanger copper alloys
in condensers and preheaters.
As regards the application, the following preservation methods have proved to be
effective:
wet preservation (see 5.2),
dry preservation (see 5.3),
inert gas blanketing (see 5.4),
volatile corrosion inhibition (see 5.5),
preservation with filming amines (see 5.6),
preservation with oil, wax, fat (see 5.7),
temporary coating (see 5.8).
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p ( t ) 100 %
w
p S
(t )
φ = relative humidity, %
pw = partial pressure of water vapour, mbar
ps = saturation pressure of water vapour, mbar
t = temperature, °C
For unsaturated air φ < 100, for saturated air φ = 100.
During the cooling of unsaturated humid air the content of water vapour and, in a first
approximation, its partial pressure will remain constant until dew point is reached. On
the assumption that all water has been removed from the system, it can be deter-
mined, by measurement of the air temperature and of the relative humidity and by
means of the figure hereafter whether, under the temperature conditions of the shut-
down system, the temperature falling below dew point and thus condensate can be
expected.
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60
5% 10 % 15 % rF
20 % rH
50
30 % rH
40 40 % rH
Temperature, in °C
50 % rH
30
100 % rH
20
10 Heating
Cooling
Drying, general
0 Drying with adsorbents
Drying with adsorption drier, (theoretical)
Starting point
-10
0 2 4 6 8 10 12 14 16 18 20
Absolute humidity, in g/kg humid air
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Atmospheric air always contains a certain amount of water (humid air) in dissolved
form (water vapour). The maximum absorbable amount of water (saturation, 100 %
relative humidity) depends on the temperature. Where the maximum absorbable
amount of water is exceeded – e.g. due to cooling of the air – condensate water will
be formed.
The figure above shows the processes that are found during heating, cooling and dry-
ing. When humid air is heated, the absolute water content will not change, and the
relative humidity decreases. When the humid air cools again or is cooled from the
starting point, the relative humidity will increase to attain the dew-point line. If cooling
continues further, condensate will be generated and the absolute water content will
decrease.
Corrosion protection by dry preservation can only be achieved with certainty if the
following requirements have been met:
In dry-preserved systems the relative humidity at the air outlet of the system
should always be less than 40 % (see Figure on p. 29 “Vernon curve”). In prac-
tice, a relative humidity less than 30 % shall be obtained in areas with corrosive
ambient conditions (e.g. plants located at the sea, in industrial areas, or the like).
No hygroscopic deposits, e.g. from salt-containing operational water or acidic hy-
drolysing layers shall be present on the walls to be protected. Prior to starting dry
preservation these deposits should be removed, if possible, because they may
affect preservation or impede the drying process.
Where non-drainable components are present in the system to be dry-preserved
which are not sufficiently exposed to the drying air flow, they shall be dried prior to
the preservation process by special measures (e.g. heating and evacuation).
All wall temperatures of the systems to be preserved shall be so high that at no
point of the system the temperature falls below dew point temperature. This may
be achieved by locally raising the ambient temperature.
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Besides easy handling and monitoring, inerting with nitrogen offers various applica-
tion possibilities.
In the case of branched systems that cannot be tightly sealed, additional cost expendi-
ture shall be considered due to increased nitrogen consumption.
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Properties Requirements
Corrosion protection properties
Internal storage (packed, storage category 2) 12 months
External storage (packed, storage category 3) ≥ 6 months
External storage (covered, storage category 4) ≥ 1 month
VOC ≤ 50 % (w/w)
Free of heavy metals < 50 mg/kg (total)
Low zinc content < 50 mg/kg
Free of molybdenum sulphide < 50 mg/kg
Low halogen and sulphur content F + Cl < 200 mg/kg
S < 200 mg/kg
Flash point (DIN EN ISO 2592) > 43 °C
No negative influence on other preservation
means or systems
Water resistance to DIN EN ISO 6270-2 min. 18 cycles
Free of CMR substances
Removability By high-pressure water or
steam-jet cleaning, or steam
Environmental influence No or only slightly environmen-
tally hazardous (= water haz-
ard class 2 or better)
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Examples for test plans to monitor preservation conditions during transport and storage as well as for plant
outages are found in the Annex.
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Preservatives intended for use in water and steam-wetted components shall be wa-
ter-soluble.
For components in contact with flue gases the preservatives should be easily remov-
able and evaporate leaving no residue. Environmental compatibility requirements,
especially at first heat input, shall be considered (no formation of combustion prod-
ucts having negative environmental effects). These points shall be taken into account
prior to applying the respective preservatives and methods.
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Fabrication/transport/storage
VCI Must be removed completely Cross-check the quantity of removed VCI Removal of solid matter
Foils, bags, pads foils/bags and pads with the quantity May normally be disposed off with do-
inserted mestic garbage/industrial waste
VCI water-soluble pow- Removal to the greatest extent possible prior As VCI powder is water-soluble, it will be Will influence the COD value of waste
der to commissioning or during pressure testing completely removed during first filling or, water
upon contact with steam with the first
condensate
VCI oily emulsion Will be removed during pressure testing or Will normally be flushed out when draining Will influence the COD value of waste
Only during fabrication/ during internal cleaning prior to commission- the pressure test water or with the de- water
transportation ing greasing solution during internal cleaning
Silica gel/desiccant Must be removed completely Cross-check the quantity of removed sili- Removal of solid matter
ca gel/bags with the quantity inserted May normally be disposed off with do-
mestic garbage/industrial waste
Wax/oil/fat Removal to the greatest extent possible 1) Remove residues, if any, with sol- Hazardous waste or oil-containing
vent/steam jet waste/disposal of oil used
Nitrogen/Inerting Take precautions regarding safety at work- none none
place (aeration/release measurements)
Temporary coatings Will usually not be removed (except for func- Mechanical removal from functional
tional surfaces) surfaces
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1) Exception: qualified preservation oils that are known to be removed from the surfaces during first fluid contact (hydrotest water, condensing
steam or rinsing oil).
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8.1 General
To reduce the expenditure of measures to a reasonable extent, individual concepts
shall be prepared.
The requirements are based on the following criteria:
classification of parts and components into hazard groups (corrosion risks de-
pending on materials)
preservation method
type of packing
storage periods
storage locations
climatic conditions in country of destination
A higher storage category shall be chosen if preservation and packing is waived for
the purpose of quicker availability.
The storage categories and the classification of parts and components into hazard
groups are described hereafter.
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8.2.1 Class A
Electrical and/or electronic material and instruments as well as other components
and parts which are especially sensitive to outside influences, require specific pre-
cautions against the following:
a) temperatures above or below the specified limits;
b) short-time temperature changes;
c) relative humidity and vapours;
d) stacking pressure and mechanical damage; and
e) contamination due to dust, sludge, faeces as well as against rain, snow and
(salty) splash water.
Parts and components to class A should be stored to category 1 or 2 in which case
the manufacturer’s instructions shall be observed.
8.2.2 Class B
Material, as for example, turbines and their components, generators, drives, electric
motors, catalysts, insulating material, ion exchange resins, which are not very sensi-
tive to outside influences, but require protection from direct influences, such as:
Material which is not very sensitive to outside influences, but requires protection
against the following impairments
a) temperatures above or below the specified limits;
b) relative humidity and vapours;
c) stacking pressure and mechanical damage; and
d) contamination due to dust, sludge, faeces as well as against rain, snow and
(salty) splash water.
Parts and components to class B should be stored to category 2 to 4 in which case
the manufacturer’s instructions shall be observed.
8.2.3 Class C
Material as for example pipe segments, feedwater tanks, pulverisers, burners, etc.
which is slightly sensitive to outside influences and requires protection from the fol-
lowing influences only:
Relatively insensitive material, but requires protection against the following impair-
ments:
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8.2.4 Class D
Material, as for example, steel construction, boiler pressure parts, flue gas ducts,
storage tanks, plastic containers, absorbers which are insensitive to ambient, climat-
ic and meteorological influences and require protection from mechanical damage
and/or ultraviolet radiation only.
The material shall be protected against direct weather influences and mechanical
damage.
Parts and components to class D should be stored to category 4 or 5 in which case
the manufacturer’s instructions shall be observed.
8.2.5 Class E
Class E covers all parts and components which are insensitive to which are insensi-
tive to ambient, climatic and meteorological influences and require protection from
mechanical damage only.
For parts and components to class E storage to category 5 will suffice in which case
the manufacturer’s instructions shall be observed.
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In the chapters to follow the various processes are explained in more detail.
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Shutdown of plant
Maintain overpressure
Preservation with steam or
With draining/partial N2 cushion
Without draining Dry preservation
draining
Dry preservation
Preservation with
operational fluid
Inspection/repairs
Filling/pressure testing
Yes Yes
Repair required? Repair required?
No No
Wet preservation
Operation
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Pourbaix diagram
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The steam gun, its supports and headers shall be designed such that the gun can be
retracted with reasonable expenditure.
The gun bores as well as header/nipple bores shall be regularly checked during peri-
odic inspections.
Increased noise development is a clear indication of erosion in the steam gun bores.
Longer steam gun service life can be obtained if high-grade steels (austenitic materi-
als) are used.
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Caution:
Access to nitrogen-preserved tanks is only permitted upon sufficient ventilation and
subsequent release of system.
The quality of preservation may be checked by O2 measurements of the nitrogen
cushion, e.g. by means of operational O2 measuring devices. An O2 content of 0.5 %
can be considered a pragmatical value for the allowable nitrogen contamination in
the preservation cycle.
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During draining care shall be taken to ensure that the water volumes drained can be
completely taken by the downstream plant parts and can be safely discharged.
The operating instructions and valid safety regulation shall be observed.
As experience has shown the pre-drying period will last approx. 10 to 20 hours. This
pre-drying process will however not suffice to obtain a low relative humidity < 40 %
required for permanent preservation. Therefore, subsequent drying by means of
dry-air blowers is necessary.
Plant parts connected to systems that remain in operation on the steam/water side
(e.g. combined-cycle plant with 2 gas turbines and one steam turbine) shall be isolat-
ed and be secured (e.g. by double block-and-bleed valve, controlled isolation sys-
tem).
Components that cannot be completely drained, e.g. very often HP preheaters are
concerned, should preferably be subjected to wet preservation as the boundary con-
ditions for successful dry preservation are generally not attained or only at a very late
stage.
Pre-drying should also be performed if e.g. dry preservation (final drying < 40 %
relative humidity) can be started only upon extended outage due to intended repair
work.
Where pre-drying has not been performed, e.g. due to unexpected changeover from
wet preservation to dry preservation, equipment with specific blowing and drying ca-
pacities shall be used to attain final dry condition in the shortest time possible.
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Then the system shall be hermetically sealed from the atmosphere, the relative hu-
midity be measured regularly and the efficiency of the silica gel be checked (for col-
our change).
The measuring results shall continuously be recorded and be evaluated.
Care shall be taken to ensure that upon completion of the preservation measures the
silica gel is completely removed from the system. The quantities inserted and the
quantities removed shall be recorded to ensure that no residues remain in the sys-
tem.
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information on oil systems and all other auxiliary and ancillary systems
electrical and I&C equipment with or without heating system
measuring techniques, transducers,
fuels and their storage systems
condensate polishing plants, cooling tower make-up water plant, DI water
systems, cooling tower
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That means that in case of extended outage where the risk of nearly complete
evaporation of residual water exists the condenser tubes shall be flushed manually
with DI water to safely prevent deposition of salt residues.
It primarily depends on the design of the cooling water system and additionally from
the condenser tube materials used, whether wet preservation with operational cool-
ing water with reduced concentration rate is performed or dry preservation only can
be done.
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In the case of foreseeable long outages (several weeks) without start-up readiness
dry preservation of the condenser is recommended independently of its design.
In case of dry preservation the tube cleaning system shall be operated shortly before
the condenser is shutdown. The condenser shall be drained and be flushed with
demineralized water directly upon draining. All manhole covers of the water boxes
or channels shall be kept open until putting into operation.
11.1.3 Materials
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During re-start the destroyed old protective layer shall compulsorily be removed (e.g.
cleaning by corundum balls) and protective layer formation be initiated anew.
11.1.3.3 Titanium
Contrary to other tube materials, the high corrosion resistance of titanium leaves
great scope of discretion.
Where no limiting factors given by the tubesheet materials or the intended corrosion
protection of the pertinent heat exchanger or cooling water system exist, an unlimited
period of outage is permitted for titanium tubes partly or completely filled with cooling
water.
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nation. Further preservation measures are not necessary. Initial rust that may devel-
op on the unprotected inner surfaces of the ACC will be flushed away during the “hot
cleaning process” (admittance of steam in by-pass operation for cleaning the air-
cooled condenser).
Upon completion of assembly the ACC should be kept dry on the inside, i.e. rain wa-
ter and humidity of the ambient air shall be prevented from entering the system.
Should the ACC not be put into operation upon hot cleaning within approx. 14 days,
measures should be taken to reduce air humidity since the inner surfaces do not yet
have any protective layer. For extended outage periods dry preservation (see below)
should be taken into account; where required, the plant should be inspected so that
further measures can be determined.
As experience has shown, a protective layer will form on the inner surfaces of air-
cooled condensers made of carbon steel despite the low pressures and temperatures
prevailing.
The formation of a protective layer is prerequisite to the steam quality meeting the
pertinent guidelines or standards (e.g. VGB-S-010).
Where outage can be planned in advance, it is advisable to raise the pH value of the
exhaust steam via feedwater dosing (volatile alkalising agent) to 9.5 or more for
some hours prior to shutdown in order to alkalise the residual water upon shutdown.
If the plant is operated with high-alkaline oxygen treatment, oxygen feeding shall be
interrupted in due time prior to plant shutdown where preservation is planned.
In the case of outages, the following preservation measures should be taken to min-
imise iron ingress into downstream systems in dependence of outage duration:
Outages up to 2 weeks: where required, let the dry air flow of the turbine drying
equipment also flow through the condenser; no additional measures necessary
Outages of 2 to 6 weeks: drain all non-automatically draining, accessible ACC
parts, tanks etc. and dry manually
Outages over 6 weeks: dry preservation of the ACC.
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during nitrogen blanketing neither the turbine shall be opened nor the ACC be
accessed for maintenance/inspection purposes.
The ACC cannot be filled completely with anti-corrosion liquids since the ACC is not
designed to withstand the weight of liquid fillings.
Drying the ACC with hot air is not technically feasible due to the great heat transfer
surface.
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12.4 Electro-deionisation
In case of electro-deionisation units care shall be taken to ensure that the resins do
not dry upon shutdown. To this end, the unit inlets and outlets shall be closed during
the time between end of fabrication and delivery as well as in case of extended non-
operational periods.
The manufacturer’s operating instructions shall be observed.
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13.1.3 Feeders
Coal feeders, discharge screw conveyors and conveyor belts as well as downshafts
shall be opened and cleaned at outages exceeding approx. 4 weeks (see 13.1.2 for
risks of damage). In case of unheated buildings, plant components underneath any
covering or within conveyors shall be appropriately ventilated to protect against con-
densation water and humidity.
Conveyor belts shall be operated several times a month.
Blank surfaces shall be protected by corrosion inhibitors, and the corrosion protection
shall be checked at regular intervals.
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Sootblowing equipment shall be blown through and then be dried with dry warm air to
obtain a residual humidity < 35 %. Then, the lines shall be dry-preserved and left
open. It is recommended to operate sootblowing equipment cyclically to ensure suffi-
cient lubrication of bearings (e.g. one operation per month).
Bearings shall remain filled with oil, the oil cooler shall be taken out of operation. The
wheel gear lubrication system shall be taken out of operation, but shall remain filled.
In case of insufficient preservation such damage as shown hereafter may occur.
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15 Flue-gas system
The flue-gas system comprises all components from the combustion chamber up to
the cooling tower flue-gas or stack entry.
15.1 Combustion chamber, convective heating surfaces and 2nd pass or blank
pass
Prior to and during the shutdown program any cleaning equipment installed for con-
vective heating surfaces furnace walls shall be operated at least once.
Upon cooling, all deposits and remaining adhesions shall be removed. When doing
so best cleaning results are obtained by wet cleaning with warm alkalised water.
Masonry, rammed lining (e.g. in the area of burners) or gaps shall be protected
accordingly against moisture. Cleaning is deemed to have ended if the washing wa-
ter is neutral or slightly alkaline. Upon wet cleaning, the combustion chamber shall be
dried which can be achieved by natural chimney draught and, where practicable, be
supported by the induced-draught fan. Caution: risk of contamination of the electro-
static precipitator hopper; put hopper heating system into operation). Alternatively,
the boiler internal space can be dried e.g. by auxiliary steam (taken e.g. from evapo-
rator tubes, steam air heater).
Should the analysis of adhesions show that they are not acidic in aqueous solutions,
wet preservation is not compulsorily required.
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Sulphuric acid will absorb water if the partial pressure of the water vapour at ambient
air is higher than the partial pressure of the water vapour of the diluted sulphuric acid.
At a still tolerable sulphuric acid concentration of 70 % H2SO4 the ambient air may
e.g. have a maximum relative humidity of 5 % so that its vapour pressure is below
the water vapour pressure of the diluted sulphuric acid (see figure above).
If the relative humidity content of the ambient air is maintained below 5 %, the sul-
phuric acid will no longer absorb water. Whether or not the reduction of the relative
ambient air humidity is effected by warming-up or drying, is of little importance for the
intended effect.
Where a residual humidity of 5 % cannot be obtained, mechanical cleaning with sub-
sequent alkaline treatment is required.
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As humidity diffusion from even far corners into the dry air flow requires a certain
time it is unreasonable to apply this preservation method for short outage periods.
Air dryers may be used in both throttled through-flow and closed-circuit operation.
In case of boilers without rotary air heater the drying equipment shall be connected
either to the flue-gas duct upstream of the stack or to the combustion chamber. In
case of boilers with rotary air heater the drying equipment shall, as a rule, be con-
nected at the air intake of the rotary air heater
When connecting the dryers, the air-intake openings of the boiler shall be closed.
The dry air will flow through the rotary air heater and the air ducts into the boiler
combustion chamber and then through the flue-gas path to the rotary air heater and
pass the boiler exit.
It is possible to have split dry air flows passed completely through the flue-gas side of
the boiler and the air-side of the rotary heater.
It will finally depend on boiler design whether decision is to be made on one or sev-
eral air flows.
The dry air supplied will absorb moisture and flow through the gaps of the incom-
pletely sealed flue-gas and air dampers of the boiler to the outside.
The dampers, however, shall be at least tight enough to allow for a slight over-
pressure in the dry-air loaded boiler such that ingress of humid air from the outside is
prevented. An extension of the outlet cross-section is possible at any time by opening
individual dampers. Where the dampers are not tight enough and the outlet cross-
section is therefore too large, inflatable plastic bubbles or plastic tarpaulins can be
used.
The humidity at critical boiler heating surfaces should be measured continuously dur-
ing the first drying processes.
During later routine operation occasional checks will suffice.
Dryers in closed-circuit operation shall be used such that the dry air enriched with
moisture from the boiler is re-directed to the dryer suction side. The moisture content
of this air on the dryer suction side will exceed the relative humidity of the outside air
upon a more or less long time so that this may lead to an accelerated drying process
compared to the aforementioned process.
During drying in throttled flow-through operation the dryer will be loaded by the out-
side air with the same relatively constant humidity
However, the air enriched with humidity from the boiler contains solid particles. This
will surely lead to the replacement of dryer air filters more frequently than is required
for the suction of air from the boiler surroundings.
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Tests have shown that at the same temperature deposits in oil-fired boilers will ab-
sorb only fractures of moisture if the humidity content of the air is low.
This is of importance for operational preservation as experience has shown that at a
relative humidity of the air less than 20 % only greatly delayed off-line corrosion will
occur.
The following measures may be taken to avoid that deposits become humid and thus
off-line corrosion is activated:
The off-line boiler is kept warm at a temperature highly above the dew point in the
flue-gas passes atmosphere thus reducing its relative humidity (thermal method).
The relative humidity of the air in the flue-gas passes is reduced by withdrawing
water (without increasing the boiler temperature) by means of suitable drying
equipment (dry-air method). As heat losses in the boiler preserved by this method
are very low, the energy expenditure required is generally lower that that required
with the thermal method.
During operation, especially during boiler shutdown, alkalising additives in excess
quantity are added so that an acid attack on the heating surface material possible
during boiler outage is minimised (chemical method).
Nevertheless, a combination of the abovementioned methods is possible.
The selection of the preservation method should depend on boiler operational re-
quirements. A boiler which e.g. is on stand-by for minutes or hour reserve shall al-
ways be kept warm. Where this boiler is, however, subject to scheduled shutdown in
the summer half-year and has to be started up in case of failure of base-load power
station units, it will be more useful to select the dry air method for economic reasons,
where practicable.
Where it is however sure that a boiler remains out of operation for a definite period of
time (as is the case e.g. in the sugar industry off-season), it may be useful to use
chemical methods, i.e. to neutralise the acid corrosive deposits by additives during
boiler plant shutdown.
In any case, the cost of the respective method should be considered. Keeping the
boiler warm is expensive unless sufficient process heat is available.
However, the costs do not always depend on the method selected, but also on the
plant condition, the quality of heat insulation, leak tightness of air and flue-gas damp-
ers, etc.
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16.4 Flue-gas side preservation of steam generators fired with substitute fuels
No generally valid information can be given on corrosion-protection measures for
steam generators fired with such fuels as biomass, residual and substitute fuels.
The causes of corrosion often are very different. Therefore, exact observation of the
heating surfaces during outages is required. Where required, the corrosive constitu-
ents of the deposits may be determined by sampling and chemical analyses. The
preventive measures to be taken shall be determined from case to case where the
aforementioned methods may also be applied.
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Examples
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Where a flue-gas damper is installed at the stack, it should be closed in any case
thus reducing convection through the gas turbine and the waste-heat boiler and min-
imising constant ingress of air humidity. Otherwise, condensation will occur in the gas
turbine and the waste-heat boiler in case of weather changes. In such cases, a tem-
porary closure of the flue-gas path by means of an “air cushion” may be effective to
prevent convection. In addition, a dry-air blower should be installed to permanently
reduce the humidity to less than 30 % relative humidity.
A further possibility of reducing the risk of off-line corrosion is keeping the boiler or
condensate preheater warm (e.g. by supplying steam to the water/steam side).
Where extensive deposits are formed, it is recommended to remove the deposits by
washing with alkalines prior to preservation, as otherwise moisture will quasi be en-
closed below the deposits and thus no defined drying process will be achieved.
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Should the storage system, however, not be monitored from the control room, it is
recommended to drain it. This can simply be done via the designated path during
DeNOx operation or via a suitable disposal system.
In this case, storage tanks, pipework as well as conveying and feeding systems shall
be cleaned (flushing with DI water) and be drained. Plants with ammonium hydroxide
evaporators will be free from NH3 due to disposal of residual liquid during the shut-
down process. Further preservation measures are not necessary in plants usually
made of stainless steels. Trace heating systems may be taken out of operation.
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17.7.5 Compressors
For short shutdown periods – up to 2 months – no specific measures need be taken.
However, care shall be taken to ensure that prior to each shutdown the compressor
is operated under suction throttle control for 15 minutes to make sure that the com-
pressor stages are subject to the so-called “dry preservation process”.
Condensation shall be avoided. The oil pump of the compressor shall be activated
once per month for approx. 5 to 10 minutes and the clutch be rotated slightly.
Long-term preservation (for up to 2.5 years) should be performed by the compressor
manufacturer.
The oxidation air compressors shall be disconnected from the system and be pre-
served for the duration of standstill.
For extended shutdown periods – 2 months and over – the screw compressor system
shall be preserved (to manufacturer’s specification).
It is recommended to perform an inspection prior to re-start.
17.7.6 Agitators
The side-entry agitators should be manually rotated to another position every 4
weeks, if possible.
The operating and maintenance instructions (agitator incl. mechanical seals) shall be
observed. Lubricating oils shall be exchanged to meet operating instructions.
Where the preservation period exceeds one year, more extensive measures may be
taken to meet manufacturer’s specifications.
Prior to re-start the manufacturer should perform an inspection.
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17.7.8.1 Hydrocyclones
All systems (incl. pipings) shall be drained and be cleaned (flushed). Where rubber-
lined components are present, possible damp environments shall be taken into ac-
count.
Plastic and rubber-lined components shall be protected from ultraviolet light and be
covered by tarpaulins, where required.
Prior to or during re-start the functionability of dampers and drives should be checked
or, in case of extended outages, the dampers should be left open.
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17.8.1.3 Preservation concept for hose-type heat exchanger systems with water as
heat transfer fluid
Short-term outages
In case of short-term outages it is important whether the outage period lies within the
cold frost season. If this is not the case, no further measures need be taken. Here, it
will suffice to further operate the circulation pumps and maintain constant pressure.
Further measures need not be taken.
Where the outage lies within the frost period, various preservation measures may be
taken to prevent frost damage on heat exchangers:
1. Filling the circuit system with anti-freeze
Only ethylene glycol can be used as anti-freeze as it will neither damage the tub-
ular bundle nor the gaskets used. However, filling of the system will produce
considerable costs. Prior to system start-up the anti-freeze shall be removed to
leave no residues. To this end, at least two flushing processes are required. The
waste water shall be disposed off to meet the respective national water conser-
vation regulations. In case of large systems, the disposal of anti-freeze without
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leaving residues will reach its limits. This removal process, even if technically
feasible, cannot be favoured on grounds of costs. In case of plastic heat
exchangers the anti-freeze will stick to the inside surfaces and will affect heat
transfer.
2. Operation of standstill heating system or connection of mobile heating system.
In some power plants, especially in northern countries with strong winters, stand-
still heating systems will be provided. In case of several power station units,
steam passes through a heat exchanger thus heating the water in the idle units.
Here, care shall be taken to ensure that the circulation pumps and the pressure
pump are further operated to distribute the heat and all valves are provided with
trace heating systems to prevent frost damage. If no standstill heating system is
available, a mobile heating system with an appropriate output may alternatively
be connected to the water circuit. In each water circuit the connection of such a
completely independently functioning heating system is possible. Such ready-to-
operate systems are supplied on trailers and only need be connected to the wa-
ter circuit. Since here considerable renting and operating costs can be expected
this possibility should be exactly calculated prior to utilizing such systems.
3. Sealing of the flue-gas duct and heating by means of heating register.
Direct heating of the tubular bundle by means of an electric heating register has
proved to be a simple and cost-effective possibility to bridge short frost periods.
At first, bulkhead walls made of blankets or thick foils should be provided to min-
imise residual cold air flows through the flue-gas duct. Then the room shall be
sufficiently heated with a heating register. At the same time, the circulation
pumps shall be operated and the trace heating system be operated at 100 %
output. The water temperature shall be monitored. However, if the water temper-
ature further decreases despite these measures and an increased heating
system output in the flue-gas duct, the connection of a mobile heating system as
standstill heating shall be taken into account as described under 2.
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Long-term outages
In case of extended outages to exceed 6 months it is advised to proceed to another
type of preservation to minimise ongoing operating costs and ensure plant safety. In
this case, the water circuit shall be drained, the bundles be disassembled and be
drained and all other components be preserved. Draining of the tube bundles in dis-
assembled condition is required, as blowing through of the bundles in assembled
condition does not ensure complete removal of water and the blowing-through
process may damage the tube bundle. In addition, the channel covers shall be re-
moved and be protected against corrosion.
Upon completion of draining, the safety valves and frost-sensitive valves shall be
disassembled and be stored dry and frost-free. The openings in the piping system
then shall be closed with plastic caps to protect the pipings usually made of unal-
loyed steel against corrosion. Flange faces shall be preserved with wax coating.
All ancillary systems shall also be preserved to meet pertinent specifications.
The table hereafter comprises the long-term preservation activities for hose-type heat
exchanger bundles. This summary does not replace careful planning of preservation
measures, but present a first guide on the work to be performed.
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In any case, the preservation of a heat exchanger system means an expenditure that
should not be underestimated and therefore should be taken into account as early as
at the planning stage of plant outages.
Especially the measures to be taken for returning to normal operating condition after
preservation are very time-consuming and in any case shall be included in the plan-
ning process for power plant re-start.
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17.8.7 Silencers
The silencers shall be cleaned by rapping and suctioning the splitter walls.
17.8.8 Stack
Drain condensate and rain water via discharge line into the FGD drain pit and pump
off, if required.
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19 Literature
Akolsin, P.A. et al: Konservierung von Hochleistungskesseln mit Stickstoff, Archiv für
Energiewirtschaft, 1965, Heft 14, S. 559-567, (Übersetzung aus: Teploenergetika, 12
(1965), S. 17-21).
Allianz-Handbuch der Schadenverhütung, Allianz Versicherungs AG, VDI-Verlag,
(1984).
Anderson, R.H.: Cost effective method mothballs a gas-fired power plant, Power
Engineering, (1987), Heft 4, S. 39-41.
Armentano, J.A., Murphy, V.P.: Corrosion protection in standby boilers, Power, 1965,
H. 1, S. 66-67.
Bieber, K.-H., Resch, G.: Vorstellung und Erläuterung der neuen VGB-Richtlinien
„Konservierung von Kraftwerksanlagen“, VGB Kraftwerkstechnik 61 (1981), Heft 7,
Seite 587-593.
Bieber, K.-H.: Einsatz und Bereitschaft von Reservekraftwerken, VGB Kraftwerks-
technik, 59 (1979), Heft 7, S. 531-539.
Bienert, J.: Kesselkonservierung mit Octadecylamin, Energietechnik, 33 (1983), Heft
1, S. 32-34.
Braunton, P.N. et al.: Neuere Erfahrungen des CEGB mit der Stillstandskonservie-
rung von Kraftwerksanlagen durch Steuerung der chemischen Umgebungseinflüsse,
VGB Kraftwerkstechnik, 60 (1980), Heft 1, S. 47-52.
British Standard Method of testing: Water used in industry, Part 117. Long-chain fatty
amines: spectrophotometric method; BS 2690: Part 117.
Bursik, A., Richter, R.: Hinweise für die Praxis der Stillstandskonservierung von
Dampferzeugern, VGB Kraftwerkstechnik, 60 (1980), Heft 9, S. 714-718.
Bursik, A., Richter, R.: Möglichkeiten der Stillstandskonservierung von Kraftwerks-
blöcken, VGB Kraftwerkstechnik, 57 (1977), Heft 4, S. 255-259.
Daucik, K.: Konservierungspraxis bei ELSAM, PowerPlant Chemistry 4 (2002), Heft
3, S. 181-182.
Glazyrin, A.I., Shchetkin, V.S.: Protection of High-pressure Drum Boilers by an
Ammoniacal Solution of Trilon B during Outage, Thermal Engineering, 32 (1985),
Heft 6, S. 337-338.
Göstenkors, T.: Konservierung von Anlagen im Kraftwerk Gersteinwerk, Der Maschi-
nenschaden, 49 (1976), Heft 6, S. 236-242.
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21 Abbreviations
Chapter 1 to 5
Abbreviation Explanation
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…………………………………………………………………………………
………………
Sonst. Maßnahmen od. 9
Ergänzungen zu/ ...............................................................................................................
Other measures or com- ........................
pletions to
Nr./No. 0-8
...............................................................................................................
........................
Erforderliche Kontrollen gemäß Teil B1-B3 :
Necessary inspection acc. Part B1-B3 :
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Komponente/Component: Anlage/Plant:
Material-Class: Storage-Category:
Konservierungsmethode: VERPACKUNGSEINHEIT
Protection method: PACKING UNIT
1 Verpackung/Packing
1.1 Zustand Kennzeichnung/Condition of designation
1.2 Zustand Kiste (n.O. = Beschädigungen, Schimmelbildung, Wassereinflüsse, ...)
2 Verpackung/Packing
2.1 Zustand Kennzeichnung/Condition of designation
2.2 Zustand Abdeckung (n.O. = Beschädigungen, unzureichende Befestigung, .....)
3.3 Überprüfbarkeit/checkability
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Prüfer/Inspector:
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Komponente/Component: Anlage/Plant:
Konservierungsmethode: VERPACKUNGSEINHEIT
Protection method: PACKING UNIT
Prüfer/Inspector:
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Komponente/Component: Anlage/Plant:
Konservierungsmethode: VERPACKUNGSEINHEIT
Protection method: PACKING UNIT
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During fabrication, transfer and shipment the following measurements shall be made
and be recorded.
Observations
Product
Measurement Date Component (e.g. appearance, Signature Remarks
content
odour)
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Example 1
Boiler filled for the last time and drains and vents checked (minimising leakage)?
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To take Munters driers of the steam turbine into operation, various release measures are re‐
quired
Have condenser hotwell/condensate lines LDK/LCA to the first isolating valve been drained acc.
to clearance document?
Date Time Initials Date Time Initials
Have condensates of auxiliary steam system downstream of the heating system been supplied
back to auxiliary boiler acc. to clearance document?
Date Time Initials Date Time Initials
Have both Munters driers of the steam turbine been installed and
been taken into operation?
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Exciter coals may be disassembled at the beginning of the 2nd week by agreement with the
electrical department. Exciter coals disassembled?
Date Time Initials Date Time Initials
Please inform absolutely promptly the E‐department
Auxiliary power transferred? as soon as the conservation will be reseted
Transformers BAT, BBT, MKC released?
Date Time Initials Date Time Initials
The date for nitrogen inerting of the boiler and the circulating pump of the water/steam circuit Attention: Absolutely shut off all cellars and MAJ
will be fixed by the power plant management. pumps areas during a restart! Nitrogen exit possible.
Has nitrogen inerting been started acc. to HMM‐XXXX?
Has circulating pump for water/steam circuit been put into operation acc. to instructions HMM‐
XXXX?
After the boiler has cooled down, the flue‐gas side drains shall be opened.
Have flue‐gas side drains been opened?
Date Time Initials Date Time Initials
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Example 2
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Trial run of both MAJ performed (If necessary, switch off Munters driers for a short time)?
Warning. Cordon‐off area around MAJ pumps during trial run! Release of nitrogen possible!
Trial run of both water vapour fans MAW80 performed
Check/ Switch over of LCL pumps to (11/12)? or trial run LCL pump (11/12)
Switched over to
PGB trial run performed (11/12) (11/12)
Date Time Initials
Operating
hours N2 gen‐
Nitrogen pressure in tank: bar erator h
m
Pressure downstream of pressure reducing valve: bar Date Time Initials
1 h trial run of PCB/PAC pump (alternately) (irrigation of cooling tower only if pH > 8.7)
PAC trial run performed (11/12)
PCB trial run performed & switched over to (11/12) Date Time Initials
In case of unit standstill all pumps (where possible) shall
be switched over acc. to “pump switch‐over instructions“
Also see Monday early shift, some equipment already been switched over!
DI water pumps switched over to (11/12):
Cooling tower make‐up water pumps switched over to (11/12): Date Time Initials
Thursday early shift:
Lube oil pump
operating
Lube oil circuit operating (21/22): (11/12):
Lube oil temp. in tank: °C Date Time Initials
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Operating
hours N2 gen‐
Nitrogen pressure in tank: bar erator h
%
O2 content: LBA80CP501 Vol LBA90CP004 % Vol HAD50CP501 % Vol
%
LBA10CP501 Vol LBB55CP002 % Vol LBA20CP004 % Vol
m
Pressure downstream of pressure reducing valve: bar
Date Time Initials
Friday early shift:
Seal oil pump
operating
Seal oil circuit operating (21/22): (11/12):
Seal oil temp. in tank: °C Date Time Initials
Operating
hours N2 gen‐
Nitrogen pressure in tank: bar erator h
m
Pressure downstream of pressure reducing valve: bar Date Time Initials
1 h trial run of PCB/PAC pump (alternately) (irrigation of cooling tower only if pH > 8.7)
PAC trial run performed (11/12)
PCB trial rum performed (11/12) Date Time Initials
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