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Degradation of The Mechanical Integrity of Steam Turbine Steels Due To Stress-Corrosion Cracking in Acidic Water

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Degradation of the mechanical integrity of steam turbine steels due to

stress-corrosion cracking in acidic water

Tim DE SERANNO1, Evelyn DE MEYER2, Arne VERLIEFDE2, Kim VERBEKEN1


1
Ghent University, Department of Materials, Textiles and Chemical Engineering,
Zwijnaarde, Belgium, Tim.DeSeranno@UGent.be, Kim.Verbeken@UGent.be
2
Ghent University, Department of Applied Analytical and Physical Chemistry,
Ghent, Belgium, Evelyn.DeMeyer@UGent.be, Arne.Verliefde@UGent.be

Abstract
Low-pressure steam turbines are susceptible to stress-corrosion cracking (SCC). The use of alternative
water sources in steam/water cycles involves an increased amount of organic compounds, leading to
higher concentrations of organic acids in the aqueous environment of steam turbine steels. The impact
of this environmental change on the mechanical integrity of steam turbine materials and the role of
organic acids in the SCC mechanism are yet not fully understood.
This review paper provides an overview of the main factors influencing SCC of low-pressure steam
turbines, i.e. material properties and the role of the acidic aqueous environment and stresses. Due to
SCC, the mechanical properties of conventional NiCrMoV steels are deteriorated. However, their
corrosion behaviour in current environments is reasonably understood and under control. Nevertheless,
they have to be re-evaluated due to continuously changing environments. Therefore, the impact of the
water chemistry, especially of organic acids, at certain temperatures and flow rates, during both
operation and shutdown conditions, still must be investigated. Stresses must be minimized and crevices
must be avoided, in which steam turbine design plays a major role.
A lot of industrial cases have been reported where cracking probably not solely occurred by
stress-corrosion, but also hydrogen embrittlement was involved. Hydrogen might play a key role in the
SCC of low-pressure steam turbines, but further research is required to determine its contribution and
evaluate the influence of organic acids.

Keywords
low-pressure steam turbines; stress-corrosion cracking; organic acids; hydrogen embrittlement

1
Introduction
In low-pressure steam turbines, the steam cools down during its adiabatic expansion and a
complex mixture of vapour and liquid phases is present [1]. The first (early) condensate can
cause significant corrosion damage to the steam turbines, including stress-corrosion cracking
(SCC) of rotors, discs and blades, which might lead to an unexpected stop of the power plant
and hence produce important operating losses [2, 3, 4, 5]. SCC is a process of metal degradation
caused by corrosion and a simultaneous sustained tensile or torsional stress. One of the first
catastrophic SCC-related failures of steam turbines took place in 1969 at the nuclear plant
Hinkley Point A in Great Britain [6]. From then onwards, turbine failure accidents have been
reported continuously, amongst others in France [7], Taiwan [8, 9], South Africa [10], USA
[11]. Since these low-pressure steam turbine failures - most of them related to SCC - frequently
occur and result in huge costs (e.g. in excess of € 100M due to a catastrophic failure in South
Africa [10]), SCC prevention of low-pressure steam turbines is of major importance.
In order to convert large amounts of heat energy into mechanical work, water is used in steam
turbines. Hence, the steam turbine materials come into contact with an aqueous environment.
Ideally, the chemistry of the water would be constant in place and time. However, water scarcity
induces the need for an increased use of alternative water sources, such as municipal or
industrial wastewater, for many different water-demanding processes, including steam/water
cycles. Such alternative water sources may have a deviating water quality compared to typically
used ground water sources, often due to the higher amounts of organic matter (total organic
carbon, TOC) in these water types, and thus require a cost- and energy intensive treatment to
meet the water quality standards, for example for boiler feed water [12]. Complete TOC
removal is not realistic and when such water types are fed into a boiler system, the elevated
temperatures in the boiler induce a breakdown of the organic compounds by hydrothermolysis,
leading amongst others to the formation of organic acids, such as formic acid and acetic acid
[13, 14, 15]. These organic acids significantly decrease the pH at the metal surface, i.e. typically
at regions where steam condensates [16, 17]. The oxide layer of the metal, which normally
allows keeping the corrosion rate under control, can therefore lose its protective nature, leading
suddenly to an exponential growth in corrosion rate [18].
The influence of the acidic aqueous environment on the mechanical integrity of low-pressure
steam turbines is not yet fully understood. In addition, the role of organic acids in the
stress-corrosion cracking mechanism still needs to be clarified. Tackling these research
questions is not self-evident, since stress-corrosion cracking is a very complex phenomenon,
influenced by many factors, such as material properties, environment and stresses present [19].
In the following three sections each of these main factors is treated. Finally, a fourth section
deals with the crack formation itself, in which hydrogen might play a key role.

Low-pressure steam turbine materials


Early steam turbine wheels in the 19th century were commonly made of cast iron [19]. A number
of early wheel failures, attributed to mechanical design factors, occurred during the 1920s [20].
Then, nickel alloyed steel was implemented as the primary wheel material. The addition of
nickel to steel increased both toughness and hardness [21]. During the early 1930s, the effect
of chromium and molybdenum on high temperature properties was fairly understood and
accepted, permitting a significant increase in steam temperature [19]. Within the same
timeframe, the stresses in the wheels began to approach a significant fraction of the yield
strength of the available steels due to the increase in rotor speed [19]. Therefore, also vanadium
was added to the steel’s chemical composition, resulting in NiCrMoV steam turbine steels.

2
By subjecting the alloyed carbon steel to a quench and temper heat treatment, chromium,
molybdenum and vanadium based precipitates can be introduced, resulting in a high strength
material with increased fracture toughness due to secondary hardening. However, these steels
are potentially susceptible to tempered martensite embrittlement (TME) [22]. TME, also known
as low-temperature temper embrittlement or 350°C embrittlement is the loss of toughness
which may occur on tempering a martensitic steel in the 250 to 400°C temperature range [22].
Therefore, only a small amount of tramp elements, such as phosphorus, is allowed [23, 24, 25].
Amongst others Holdsworth et al. [26] and Lyle et al. [27] reported that phosphorus and other
residual elements also influenced stress-corrosion crack growth kinetics. In contrast, according
to Speidel et al. [28, 29], neither the steel cleanliness, nor the base composition influenced the
growth of stress-corrosion cracks in low alloy steels when exposed to hot water. The plausible
independence of base element content, such as molybdenum, on the SCC crack growth is
remarkable, as Gras et al. [7] indicated later on that general corrosion of Mo-containing steels
could generate molybdic acid, which might play a role in the SCC mechanism.
During the 1960s, the mechanical properties of the low-pressure steam turbines were even more
enhanced, by lowering the austenitizing temperature to achieve a finer grain size, as such
improving strength and toughness [19]. In order to obtain an improved transformation structure,
the content of nickel, which is an austenite stabilizing element, was increased, whereas the
ferrite stabilizing molybdenum content was reduced [19].
In the 20th century, extensive research in the area of steam turbine material’s susceptibility to
cracking in turbine environments has been conducted, resulting in several NiCrMoV steels,
which are nowadays still used. Especially 3.5NiCrMoV steel is often used for steam turbine
rotors and discs, while 12Cr stainless steels are often used for blades [10]. Generally, these
steels have a martensitic structure, because austenitic steels are not appropriate due to their low
damping capacity and relatively high thermal expansion coefficients [30]. Sometimes also
precipitation hardened stainless steels are used for steam turbine blades, although they may be
difficult to weld and be prone to selective dissolution, as such forming pits which can act as
crack initiation sites [31].
Besides the conventional NiCrMoV steels, also developments concerning improved
aerodynamics of the last row blades increased the necessity of higher strength alloys [32].
However, with increased yield strength of high strength steels usually the susceptibility to
environment induced cracking increases and crack propagation is much faster [4, 32, 33]. The
crack growth rate at higher yield strength can even be several orders of magnitude larger than
for lower yield strength materials. For this reason, many power plants had to replace their steam
turbine discs with a lower strength material because of the danger for SCC failure [31]. The
yield strength is reported to be the dominant material factor governing SCC [34]. Consequently,
applicable steels for especially rotors, discs and blades seem to be limited in yield strength.
However, in the meantime, some turbine materials with higher strength have been developed.
For example, the use of titanium alloy blades, e.g. Ti-6Al-4V, for the last stages of low-pressure
steam turbines are used and some others are under investigation [31, 35, 36]. Such titanium
blades can have similar yield strength as the steels, are a lot lighter and would have a better
corrosion resistance, including a better behaviour regarding SCC during operation in wet steam
[36, 37, 38]. However, they are significantly more expensive, difficult to machine, more brittle,
have a low material damping and might be more prone to scratches [31, 37]. Protective coatings
for steam turbines are also sometimes used [39, 40, 41, 42, 43]. The behaviour of advanced
steam turbine steels in steam/water conditions still needs thorough investigations before actual
implementation in industry is possible. Even the corrosion behaviour of the currently used
steam turbine steels still needs to be investigated, because of possible variations in the
environments in which they are used.

3
Acidic aqueous environment
Over the last few decades, a gradual change in the environment in which steam turbine steels
are used has occurred, due to for instance new water treatment practices and the ongoing shift
towards alternative water sources. Steam turbine steels acting as high-performant in certain
environments, may fail in other environments. Indeed, minor changes in the environment can
have a large impact on the corrosion behaviour. Factors of major importance concerning the
environment are, amongst others, its chemistry, temperature and flow rate. In this section, first
the chemistry of the environment is treated, including the presence of dissolved gases and
impurities. Subsequently, SCC dependence on temperature and flow rate is discussed. The last
part of this section deals with the importance of shutdown conditions.
Dissolved gases
Several dissolved gases, such as O2, CO2 and H2S, might influence the stress-corrosion cracking
of steam turbine steels. In the late 20th century, the contradicting impact of dissolved gases on
SCC of steam turbine materials was reported. Stress-corrosion crack growth rates of rotor disc
steel measured by Speidel et al. [28] showed no dependence on oxygen concentration or on
CO2 level. In addition, calculations of Liu et al. [5] showed that the initiation and propagation
of stress-corrosion cracking was not very sensitive to the oxygen content of the steam. In
contrast, McMinn et al. [44] reported a strong relationship between cracking and the
concentration of oxygen in the steam/water system of power plants. According to Schleithoff
[45], CO2 had an important influence on the crack development.
In the beginning of the 21st century some more insight was gained on the influence of dissolved
gases on SCC of steam turbines. Maeng et al. [46] noted an increase of the SCC susceptibility
of typical 3.5NiCrMoV steam turbine steels in environments with higher dissolved oxygen
content, by performing constant elongation rate tests in high temperature water of various
dissolved oxygen concentrations. However, Dooley [47, 48] reported that oxygen does not
concentrate in the first condensate, i.e. oxygen levels in the first condensate might be lower
than 1 ppb for steam inlet oxygen levels of 30-250 ppb. This low oxygen content in the first
condensate is due to the partitioning of oxygen between the steam and liquid phases [48]. In
terms of corrosion research this had an impact on the potential corrosion mechanisms of steam
turbines. Consequently, the main thinking in scientific research shifted from steam turbine
corrosion caused by high oxygen levels towards other factors of the environment that are
dominant for the corrosion of steam turbine materials, especially steam purity, temperature,
flow rate and shutdown conditions.
Guidelines for industry nowadays recommend a maximum oxygen concentration of a few
hundred ppb [49, 50]. Deoxygenation can be done by use of e.g. deaerators and oxygen
scavengers, such as hydrazine. However, at some places the use of hydrazine was abandoned
to enhance the resistance of the magnetite layer to flow-accelerated corrosion (FAC) [51]. It is
recommended to also remove other dissolved gases, such as H2S. Especially in geothermal
steam turbines, a non-negligible amount of H2S most often is present, leading to corrosion of
turbine materials [42, 43, 52, 53].
Impurities
A lot of contaminants, such as hydroxides, sodium, chlorides, carbonates, acids, hydrogen,
sulphur, etc. may be present in the steam/water cycle, originating from multiple sources.
Besides entering the steam/water cycle along with the feed water, originating from condenser
leaks or from condensate polishers, they could also be present due to manufacturing, storage,
installation or inspection of steam turbine parts [31].

4
NaOH is referred to be the most corrosive contaminant with respect to SCC of low-pressure
steam turbines [54]. It may have originated from high boiler carryover while improper boiler
water control and from malfunctioning condensate polishers and makeup systems [31].
According to Lyle [55], addition of small amounts of NaCl reduced the concentration of NaOH
necessary to produce SCC of 3.5NiCrMoV steam turbine steel.
Besides the impact such contaminants can have on the corrosion behaviour of steam turbines,
a lot of them also can thermally decompose into acids such as organic, carbonic, sulphuric,
hydrochloric and molybdic acid [31]. Molybdic acid can be formed from MoS2, often used as
thread lubricant, and might cause SCC of NiCrMoV shrunk-on discs [7]. Consequently, such
corrosive lubricants have to be eliminated from use in steam/water cycles.
To get rid of a lot of contaminants, the feed water must be subjected to an appropriate water
treatment before entering the steam/water cycle. Also during operation the water must be treated
adequately, such as with condensate polishers and by performing boiler blowdowns. However,
steam/water cycles are most often under pH control for protection of preboiler and boiler
equipment. Consequently, it might be that this does not match with the requirements of the
steam turbine surfaces. Care must be taken that the removal or addition of certain species in the
water is reasoned for the sake of the whole steam/water cycle.
Nowadays, film-forming amines are often used as barrier inhibitors to slow down the corrosion
rate. Van Lier et al. [51] stated that in a film-forming amine treated steam/water cycle not only
caustic gouging and acid phosphate corrosion did not occur, but also that the risk of hydrogen
damage was vastly reduced by the continuous removal of deposits. Moreover, film-forming
amines might have a mitigating effect on both flow-accelerated corrosion and corrosion-fatigue,
based on evidence presented by Lister et al. [56] and Povarov et al. [57], respectively. Although
these film-forming amines form a protective layer against corrosion by adsorption on the wall,
it is still unknown what the exact protection mechanisms are and whether these amines also are
a source of corrosive organic acids themselves when they thermally degrade [58].
A good control of water chemistry is vital in preventing problems in a steam/water cycle system.
However, very dilute solutions in the steam/water cycle can become concentrated during
operation. As shown in Figure 1 [59], a steam turbine is normally part of a steam/water cycle.
When certain species get concentrated, even due to very small incremental increases in each
cycle, the chemistry of the environment of the steam turbines can be significantly changed and
corrosion can be promoted. Dooley et al. [60] stated that “cycle chemistry is responsible for
about 50% of the failures in fossil plants and about 70% in combined cycle units with HRSG”
[51].
Not only concentrating of impurities due to the cyclic process must be taken into account, but
also locally impurities can concentrate, e.g. in the first condensate. Indeed, the exhaust pressure
of low-pressure turbines is often designed to be sub-atmospheric, in order to gain the maximum
energy output [61]. When the steam, flowing through the low-pressure steam turbine, expands
and crosses the saturation line (Wilson line), moisture droplets nucleate. Although the
properties of such first condensate droplets are yet not fully understood, some things can be
said about the steam-water partitioning. Ionic impurities, which are usually present in low
concentrations in the steam, can concentrate by factors of more than one hundred in the liquid
phase [17, 62]. Also anionic impurities might be concentrated in the liquid phase, leading to a
reduced pH of the first condensate [48]. For example organic acids can transport from the
vapour to the liquid phase due to their low distribution coefficients [63].

5
Figure 1. Schematic drawing of a steam/water cycle [59].

A common organic acid found in the first condensate is acetic acid. Concentrations of about
600 up to 6000 ppb of acetate were found in the first condensate by performing first condensate
sampling experiments [3, 17]. According to Wei et al. [63], the concentration of acetic acid in
the first condensate is more than 1000 times higher than that in the inlet steam, resulting in a
lowered pH of the liquid phase. Maeng et al. [64] showed that the presence of acetic acid
facilitates SCC of typical 3.5NiCrMoV steam turbine steel by performing constant extension
rate tests in hot water. However, at very high concentrations SCC susceptibility was again
lowered because excessive dissolution induced crack blunting [64]. Also in first condensates
containing chloride ions, acetic acid would play a key role in the initiation and propagation of
pits by decreasing the pitting resistance and increasing the corrosion rate of 2Cr12MoV steam
turbine steel [63]. Other organic acids can be formed as well. For example ethanolamine, often
used as pH-conditioner and chelating agent in low-pressure steam turbines, can thermally
decompose to organic acids, such as acetic acid, formic acid and galactic acid [64].
Besides steam-water partitioning during condensation, also deposition due to exceeding of
steam solubility limits during steam expansion or even local evaporation of moisture, might
lead to increased impurity concentrations [19, 31]. After all, a lot of parameters controlling
corrosion, such as pH and temperature, can change within a broad range in the steam turbine.
Temperature
The temperature can have a large impact on the stress-corrosion cracking of low-pressure steam
turbines. Maeng et al. [46] reported that the SCC susceptibility of 3.5NiCrMoV steel increased
with increasing temperature. The elongation and maximum stress of the steel decreased as
temperature increased. The temperature would speed up the rate-controlling step of the SCC of
steam turbine steels [46]. Test results of Lyle [55] indicated that the minimum sodium
hydroxide concentration required to produce detectable SCC decreased with increasing
temperature.

6
Flow rate
Also the relative velocity of the environment with respect to steam turbine material affects the
corrosion behaviour. Especially in stagnant areas, solutions can concentrate and remain for long
periods during operation [19, 46].
Beside regions without or with hardly any flow, too high flow velocities can also be
problematic. Indeed, the flow velocity of the wet steam may not exceed the allowable velocity
specific to the turbine materials and moisture chemistry, in order to avoid flow-accelerated
corrosion. Therefore, regions of high turbulence must be avoided. Another way to avoid FAC
might be the use of steels containing enough chromium – and maybe also other alloying
elements - to form a protective oxide layer which keeps its integrity in such circumstances [31,
65]. Also the control of the water chemistry, e.g. reducing organic acids and as such increasing
the pH of the first condensate, could result in less FAC [31].
Another flow rate related problem is water droplet erosion, particularly in the last stage of the
low-pressure steam turbines. The blades, rotating with high velocity, get damaged because they
hit condensed water droplets. The pH, amongst others influenced by the concentration of acids,
was found to have a large impact on the erosion rate [66, 67].
Shutdown conditions
During shutdown the environment can be totally different with respect to the environment
during operation, leading to alternative forms of corrosion. During unprotected layup, corrosive
deposits can be present due to an increased humidity and oxygen content present in the aqueous
environment in contact with the steam turbine materials. This can lead to pitting of especially
disc-blade attachments and steam turbine blades, particularly in the phase transition zone (salt
zone) [31]. Little pitting is observed on wet stages because impurities can be washed away. In
contrast, at places where impurities can almost not be removed, such as in blade tenon-shroud
crevices, pitting is frequently observed [31]. Pitting can be the precursor to more extensive
damage such as SCC and corrosion fatigue [48]. To reduce the chances of pitting during
shutdowns, specific equipment can be installed, such as recirculation systems for pressure
sections, nitrogen generators, dehumidification systems and gas-transfer membrane skids [68].
In addition, the selection of titanium alloy blades is recommended, due to their good resistance
against pitting.
Concerning the corrosive impact of the environment on steam turbine materials, as well the
environment during operation as the environment during shutdown needs to be taken into
account. For both environments, steam purity is of major importance and has to be kept under
control. Although it is not possible to remove every single impurity (organic contaminants
which form organic acids can still be present) at all times the steam/water composition should
be known. A real-time appropriate water treatment should be performed based on the
instantaneous steam/water chemistry. Also awareness of local temperatures and flow rates is
recommended. In addition, the currently used steam turbine materials need to be re-evaluated,
taking into account their changing environments. For this, a better understanding of the role of
different features of the material microstructure in the mechanical degradation of low-pressure
steam turbine steels due to SCC may be evaluated by performing experiments based on the
methodology developed by Depover et al. [69, 70, 71, 72, 73, 74]. They characterized the
impact of an environment, in their case the presence of hydrogen, on the mechanical integrity
of several steels by performing constant extension rate tests with in-situ hydrogen charging.

7
Stresses
Besides the corrosive environment, stresses are also needed for a steam turbine to suffer from
SCC. A first aspect related to the stresses in steam turbine materials is the design of the steam
turbines. For example steam turbine blade root designs have geometries with stress
concentrations that promote SCC. In order to minimize local tensile stresses, those steam
turbine parts can be shot-peened. As a result, compressive residual stresses are generated at the
surface, which can resist crack initiation [10, 42, 43]. However, tensile stresses are consequently
present in the subsurface region. When the compressive layer gets damaged up to the region of
these induced tensile stresses, corrosion might even be enhanced.
Although design parameters may be well advanced for material behaviour and aerodynamics,
they might also induce undesirable impurity concentrations. Especially crevices can act as
impurity traps and in addition they also facilitate the formation of oxygen concentration cells
and generate high stresses. Therefore, crevices must be avoided as much as possible. For this
purpose, it might be better to use large parts instead of a lot of small parts assembled together,
e.g. solid turbine parts instead of built-up or shrunk-on parts. In addition, a large advantage of
one-piece-parts is that they are made of only one material, because combination of dissimilar
materials in contact can produce galvanic corrosion and must therefore better be avoided.
Another advantage of solid turbine parts, e.g. solid rotors, is that they do not suffer from disc
bore SCC as shrunk-on discs do [31].
A third possible type of low-pressure rotors are welded rotors, as shown in Figure 2 [75]. These
are also a good option in order to eliminate the high stresses in disc keyways of shrunk-on discs
[76]. Besides welding of steam turbine parts, also weld repair with amongst others 12Cr steel
is often performed [65]. However, welding influences the properties of the base material in the
heat affected zone and may introduce internal stresses [77]. In this way also the corrosion
behaviour of the steels can be changed [78]. In addition, welding is a possible cause for the
entry of hydrogen into the material, leading to metal degradation [79, 80]. Hydrogen can be
picked up in the molten weld pool because of dissociation of hydrogen gas, water or
hydrocarbons [81]. Upon solidification, the hydrogen remains trapped in the material and
consecutively causes a degradation of the material [82].

Figure 2. Three types of construction for low-pressure rotors [75].


Besides the design stresses, for example steam turbine discs can also have some residual
stresses from machining, vibratory stresses and stresses due to centrifugal loads by rotor
rotation. Minimization of stresses can have a large influence on the sensitivity to
stress-corrosion cracking. A well-chosen design can make a huge difference in the SCC of
steam turbines by amongst others minimizing stresses and avoiding crevices.

8
Cracking
The cracking of steam turbine steels occurs predominantly intergranularly and cracks are often
branched [83]. McMinn [44], for instance, reported intergranular cracking along the prior
austenite grain boundaries. Hodge and Mogford [84] also observed that cracking in UK steam
turbines was mainly intergranular, although the crack initiation was usually transgranular.
Fractures due to SCC are typically brittle [65] and several SCC mechanisms have been
proposed: film-rupture mechanisms [85, 86], mechanically assisted chemical dissolution
mechanisms [87], strain induced corrosion cracking mechanisms [88] and hydrogen
(embrittlement) assisted cracking mechanisms [89, 90]. A key factor in the latter type of
mechanisms is hydrogen, which might play an important role in stress-corrosion cracking.
Hydrogen is able to absorb into the metal and diffuse to regions ahead of the crack tip, as such
accelerating the crack propagation. Hydrogen embrittlement (HE), characterized by a hydrogen
induced ductility loss, is known to cause unpredictable failure.
HE in steam turbines
During the 1950s already, the fracture of a low-pressure steam turbine rotor made of NiCrMoV
steel was reported to be initiated from crack-like flaws, apparently caused by hydrogen damage
[19]. When experts studied the cracks found in both burst and intact discs of the catastrophic
SCC-related steam turbine failure at the nuclear plant Hinkley Point A in Great Britain, they
concluded that cracking probably did not solely happen by stress-corrosion, but that hydrogen
embrittlement might have had a relevant contribution as well [6]. Also after performing tests
related to the steam turbine failure in France in the 1990s, Gras et al. [7] stated that the
stress-corrosion cracking mechanism probably involved hydrogen embrittlement. Although
hydrogen can readily enter steam turbine materials during processing, welding or in service,
necessary precautions have not been taken so far [79, 80, 81, 82].
Bavarian et al. [91] reported that turbine rotors, discs and blades made of high strength steels
suffered from both stress-corrosion cracking and hydrogen embrittlement. Speidel et al. [28]
argued that the propagation of stress-corrosion cracking in high strength materials was
significantly accelerated by the local presence of hydrogen. According to them [28], the
embrittlement by hydrogen of low-pressure rotor steel can be interpreted as an ‘alloying effect’,
changing the properties of the material and accelerating crack propagation [92, 93].
By fractographic analysis of linearly increasing stress tested 3.5NiCrMoV steam turbine steel
in distilled water at 90°C, Ramamurthy et al. [94] proposed a strain induced anodic dissolution
mechanism at these conditions. However, when performing similar tests at temperatures below
60°C, hydrogen, coming from the cathodic reaction, was believed to play a role in the
mechanism by embrittling the region ahead of the crack tip [95, 96]. This was confirmed by
Liu et al. [97], who detected hydrogen associated brittle fracture events after the onset of
necking of 3.5NiCrMoV steel, when performing the same tests at room temperature and at
negative applied potentials, as such isolating the cathodic reaction. Consequently, this indicated
that hydrogen might play a role in the SCC mechanism of low-pressure steam turbine steels at
room temperature. However, it must be clarified whether hydrogen also plays a role in the SCC
mechanism at higher temperatures, i.e. around 90°C, since at those temperatures the most SCC
low-pressure steam turbine problems have been reported.
In addition, the fundamental effect of several factors, such as water chemistry and flow rate,
still needs to be investigated. Particularly, the impact of organic acids in nowadays changing
aqueous environments on the (hydrogen assisted) SCC mechanism should be determined,
taking into account the complex structure of the low-pressure steam turbine materials.

9
Acknowledgements
This work was performed in the framework of the IMPROVED project. The IMPROVED
project is subvented by The interreg V “Vlaanderen-Nederland” program, a program for
transregional collaboration with financial support from the European Regional Development
Fund. More info: www.grensregio.eu
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