Research Article | Open Access
Rickard R. Shen, Bartek Kaplan, Pål Efsing, "Experimental and Theoretical Investigation of Three Alloy 690 Mockup Components: Base Metal and Welding Induced Changes", International Journal of Nuclear Energy, vol. 2014, Article ID 504927, 9 pages, 2014. https://doi.org/10.1155/2014/504927
Experimental and Theoretical Investigation of Three Alloy 690 Mockup Components: Base Metal and Welding Induced Changes
The stress corrosion cracking (SCC) resistance of cold deformed thermally treated (TT) Alloy 690 has been questioned in recent years. As a step towards understanding its relevancy for weld deformed Alloy 690 in operating plants, Alloy 690 base metal and heat affected zone (HAZ) microstructures of three mockup components have been studied. All mockups were manufactured using commercial heats and welding procedures in order to attain results relevant to the materials in the field. Thermodynamic calculations were performed to add confidence in phase identification as well as understanding of the evolution of the microstructure with temperature. Ti(C,N) banding was found in all materials. Bands with few large Ti(C,N) precipitates had negligible effect on the microstructure, whereas bands consisting of numerous small precipitates were associated with locally finer grains and coarser grain boundary carbides. The Ti(C,N) remained unaffected in the HAZ while the carbides were fully dissolved close to the fusion line. Cold deformed solution annealed Alloy 690 is believed to be a better representation of this region than cold deformed TT Alloy 690.
Many components in pressurized water reactors (PWRs) today are made of Ni-base alloys, for example, control rod drive mechanism (CRDM) nozzles, steam generator (SG) tubing, and SG divider plates. These components were previously made of Alloy 600 since it had exhibited good corrosion resistance in many aggressive environments in combination with having a coefficient of thermal expansion close to that of steel. Unfortunately, Alloy 600 soon turned out to be susceptible to stress corrosion cracking (SCC) in primary water, having a case reported in field in 1971 after only two years in service .
Alloy 690 was developed as a remedy to the SCC in Alloy 600, essentially being a high Cr version of Alloy 600 containing nominally 30% Cr instead of around 15-16%. Since the SCC resistance of Alloy 600 was found to significantly increase after being thermally treated (TT) [2–4], that is, heat treated for precipitation of a semicontinuous carbide network along the grain boundaries, Alloy 690 has also been used in the TT state. TT Alloy 690 has been used in operating plants since 1989, and no cracking due to SCC has been reported to date. From both operational experience and laboratory experiments, it is evident that Alloy 690 has considerably higher SCC initiation resistance than its predecessor [2–4]. Experiments in recent years have however shown that it is possible to induce high SCC crack propagation rates in simulated primary water, comparable to those of Alloy 600, but only when the tested material had been heavily cold worked prior to testing, for example, by cold rolling or forging [5–7].
Earlier experiments on cold worked TT Alloy 690 were part of an exploration of the effects of plastic strain on SCC in primary water. While Alloy 690 is not used in an intentionally cold worked state, the experiments were instead motivated by the concern for the heat affected zone (HAZ) of welded Alloy 690, which experiences high levels of plastic straining due to weld shrinkage, and can be further increased by repair welds. Estimates based on electron backscattered diffraction (EBSD) measurements have shown that the effective plastic strain in the HAZ typically increases towards a maximum around the fusion line [7, 8]. The maximum can often reach levels comparable with 20–30% thickness reduction by cold rolling or forging, that is, the levels of deformation for which high crack growth rates have been observed in experiments.
Although cold working TT Alloy 690 base metal can generate a material with similar hardness and dislocation density as in the HAZ, the microstructural changes caused by the thermal cycles of a welding process would be absent. It has been shown that cold working Alloy 690 in a solution annealed (SA) state, where the M23C6 carbides have been dissolved, is not nearly as detrimental to SCC resistance as the same cold work performed in the TT state, where the grain boundaries would instead be densely covered in carbides [7, 9, 10]. Recent SCC crack growth experiments on the Alloy 690 HAZ itself also show much lower crack growth rates than in cold worked TT Alloy 690 base metals despite the high innate plastic strains of the HAZ [7, 11]. The results suggest that plastic strain by itself cannot explain the high crack growth rates. Synergetic effects of cold work and microstructural features, for example, banding phenomena, cracking of intergranular carbides, and strain localization at grain boundaries, have thus attracted increased attention in recent years [9, 12, 13].
How the differences in strain and thermal history affect the microstructure is an important step in understanding to which extent results obtained using cold worked materials can be extrapolated to describe HAZ behavior. The microstructure in the cold worked state has been described in literature and often exhibits damage such as cracked particles, particle-matrix interface debonding, grain boundary cavitation, or strain localization at particles and grain boundaries [9, 10, 13]. In this work, thick-walled TT Alloy 690 base metals without addition of cold work have been characterized along with their respective HAZs using materials representative to those found in operating plants. The aim of this work was to identify the microstructural changes induced by welding and discuss the suitability of using cold worked TT Alloy 690 to simulate the HAZ. In order to attain a complete picture of the alloy, the equilibrium composition and fractions of the constituent phases were also investigated using thermodynamic calculations and compared with the experimental observations.
2. Experimental Details
2.1. Fabrication of Mockups
Segments of three mockup components from different manufacturers were provided for this work. All three mockups have been produced using commercial heats, realistic designs, and welding procedure specifications approved for actual plant components. Any observations made in this work are therefore expected to be found in materials in operating plants as well. Figure 1 shows photos of the mockups and what they represent in a PWR plant. In this work, the three mockups are referred to as(i)CRDM1—CRDM nozzle penetration mockup with the Alloy 690 tube inserted straight through a low alloy steel plate,(ii)CRDM2—CRDM nozzle penetration mockup with the Alloy 690 tube inserted at a 46.5° angle through a low alloy steel plate,(iii)DP—a one inch thick cross-sectional slice of an Alloy 690 SG divider plate mockup.
All Alloy 690 base metals were welded in the as-received state, that is, hot worked followed by a SA and TT. The SA aimed at dissolving the carbides and is typically performed at around 1050°C for up to an hour followed by a water quench. The purpose of the TT is to precipitate carbides at the grain boundaries, which is achieved by several hours at around 700°C. These heat treatments also serve to recover the material and to relieve elastic stresses. The chemical compositions of the Alloy 690 base metals which used the mockups are given in Table 1.
CRDM1 was manufactured using a hot extruded TT Alloy 690 tube inserted straight through a SA 533 grade B steel plate that was clad in grade 308 L stainless steel on the simulated internal surface, representing the reactor pressure vessel head. The tube had an outer diameter of 100 mm and a wall thickness of 16 mm. The tube was attached to the steel plate by gas tungsten arc welding (GTAW) with Alloy 52 M using a J-groove weld. A schematic sketch of the J-groove weld is shown in Figure 2(a). The completed weld was inspected using penetrant testing (PT) and ultrasonic testing (UT).
CRDM2 was manufactured in a similar manner as CRDM1, but by a different manufacturer, and using a TT Alloy 690 tube inserted at a 46.5° angle through an SA 508 grade 3 steel plate instead of straight through. The tube was also hot extruded and had similar dimensions as the CRDM1 tube. Furthermore, no stainless steel cladding was applied on the steel plate, and Alloy 52 was used to fill the J-groove weld of this mockup. The completed weld joint was inspected using PT and UT.
The DP mockup had a steel bar as a base, representing the bottom end of a SG, buttered with a roughly 2 cm thick layer of Alloy 52 M. A hot forged bar of TT Alloy 690 was used to represent a SG divider plate. The bar was 132 mm thick in the S-direction, 105 mm in the T-direction, and roughly 410 mm long. The TT Alloy 690 bar was oriented as shown in Figure 2(b) and welded to the steel bar by GTAW with Alloy 52 using a double beveled groove. The completed weld was inspected using PT and UT.
2.2. Microstructural Characterization
In this work, the longitudinal, circumferential, and radial directions have been denoted by L, C, and R, respectively, for the tube materials. For the TT Alloy 690 bar used in DP, the longitudinal, long-transverse, and short-transverse directions have been denoted by L, T, and S, respectively. In order to study the possibility of microstructural anisotropy in the base metal, metallographic specimens were prepared with planes normal to the three orthogonal directions mentioned above. For characterization of the unaffected base metal, material sampled far from the weld was used to ensure minimal influence from the weld process. Specimens for HAZ characterization were prepared using material sampled near the weld root, where the weld induced plastic strains typically are significant. All samples were cut out of the mockups with care using plenty of coolant and low cutting speed to avoid unwanted evolution of heat.
The sampled materials were mounted in conductive plastic resin, ground on SiC paper, and polished on a rotating cloth disc with diamond suspension. The samples were investigated both in the as-polished condition and after being electrolytically etched in a nital solution (5% nitric acid in ethanol) with 4 V applied anodically for 15–25 s. The samples were studied in a light optical microscope (LOM) with optional dark field filter and in a scanning electron microscope (SEM) equipped with a backscattered electron (BSE) detector and equipment for energy dispersive X-ray spectroscopy (EDX).
Apart from the matrix, M23C6 type Cr-rich carbides and TiN/Ti(C,N) precipitates were assumed to be the only phases of significance in the material. These were differentiated in LOM by their color since TiN/Ti(C,N) appear golden or orange, while the Cr-rich carbides appear grey. High enough magnification is important as both phases appear as dark spots at insufficient magnification. They were also differentiated in SEM by atomic number contrast. The average atomic number of Ti(C,N) is significantly lower than M23C6, which results in a much darker color in the SEM using a BSE detector. EDX was used as a supplement in SEM to confirm locally elevated Ti or Cr levels at the particles for additional confidence in the phase identification.
Uneven illumination caused by the light source, lens system, and camera, for example, vignetting and hue gradients across the image, can affect the perception of hues in the LOM micrographs. The illumination over the image was quantified by fitting a second-order polynomial surface to the pixel intensities for each of the red, green, and blue color channels, respectively, over the image. Since Alloy 690 has a single phase matrix, such a fit of an ideal image would result in a flat plane for each color channel. All three fits would also be of similar intensity since they represent the grey color of the matrix. For each color channel, the fitted surface was divided by its mean value over the image to obtain a normalized division filter, which was used to compensate for the uneven illumination. Note that this method does not introduce any artifacts to, nor remove any details from, the images.
3. Thermodynamic Calculations
Thermodynamic calculations were applied in the present work in order to investigate the equilibrium phase fractions and the composition of each individual phase, with focus on the M23C6 carbide and the Ti(C,N) nitride/carbonitride precipitates. The considered alloy compositions were the same as shown in Table 1, excluding Mn, S, and P as explained below.
The thermodynamic calculations presented in this work were performed using the Thermo-Calc software package  together with the Ni-based Superalloys database version 5 (TCNI5) available from Thermo-Calc Software. The database contains critically assessed thermodynamic parameters that make up the Gibbs energy of each phase as a function of temperature, pressure, and composition. Roughly, the calculations are based on minimization of the Gibbs energy functions of the system subject to some user defined constraints to find, for example, the fractions and composition of phases present when the equilibrium state is achieved. These quantities, as well as many others, can then be visualized as a function of, for example, temperature or average composition.
Calculations such as these are strongly limited by the quality of the database used, which is why the choice of database is critical. In the case of TCNI5, the database does not include Mn, P, and S. However, these elements are only present in small quantities in the investigated alloys and were assumed to have little or no effect on the stability of the phases of interest.
4. Results and Discussion
4.1. Unaffected Base Metal
The TT Alloy 690 tube of CRDM1 was homogeneous and had an equiaxed grain structure with plenty of annealing twins. The grain boundaries were densely covered by a network of Cr-rich carbides. Intragranular carbides were observed but very rarely. It is commonly accepted that these Cr-rich carbides in Alloy 690 are of the M23C6 type [2, 15], which agrees well with the thermodynamic calculations; see Section 4.3. Fairly large faceted precipitates of sizes up to around 10 μm were common in the microstructure and appeared orange in LOM as shown in Figure 3. These are generally accepted as TiN or Ti(C,N). Since Lengauer et al. have shown that pure TiN has a golden color, which it gradually loses as carbon content increases , these precipitates will be denoted by Ti(C,N) in this work.
The Ti(C,N) precipitates were often found concentrated in bands extending in the L-direction of the tube. These bands were nonetheless faint in this material and easily missed. Many of the precipitates also appeared elongated in shape along the L-direction. Virtually no free oxide inclusions were observed in the base metal, although oxide slags were frequently found at the core of the larger Ti(C,N) precipitates.
The microstructure of the TT Alloy 690 tube of CRDM2 was similar to that of the tube of CRDM1, having an equiaxed grain structure with plenty of annealing twins and with grain boundaries densely decorated by carbides. Large Ti(C,N) precipitates of comparable size as those in CRDM1 were also present, but fewer in number. The differences between these tubes were mainly related to particle banding, which was significantly more distinct in this tube than in CRDM1. In particular, the bands contained plenty of small intragranular particles, up to around 1 μm in diameter, in addition to the large Ti(C,N) precipitates. As can be seen in Figure 4, the bands were extending in the L-direction as columns. These bands were especially easy to see in LOM using a dark field filter. Note also that the banding can be difficult to see if the material is only sectioned in the R-C-plane.
The small intragranular particles in the bands were also believed to be Ti(C,N). They also had an orange color in LOM, and EDX confirmed clearly elevated Ti levels at these particles. Table 2 shows the distinct difference in Cr and Ti levels for these two types of particles, although their limited sizes did not allow for a quantitative chemical analysis. The Ti(C,N) also appeared noticeably darker in SEM using a BSE detector compared to M23C6 carbides, agreeing well with it being a phase with lower average atomic number. Despite the large number of fine Ti(C,N) precipitates, the total volume fraction of this phase still appeared to be less than in CRDM1 due to a lower number of large Ti(C,N) precipitates. This correlates well with the lower N and Ti content in the CRDM2 tube shown in Table 1.
|ND = not detected.|
The grain size tended to be smaller within the Ti(C,N) banded regions. This resulted in a bimodal grain size distribution in the CRDM2 tube, although the average grain size was comparable to that of the CRDM1 tube. Grain boundaries could be seen lining up along bands fairly commonly, forming relatively straight lines ranging up to around 1 mm; see Figure 5. This sort of grain boundary alignment was observed throughout the material, but always within a band, or along the edge of a band. These observations indicate that Ti(C,N) precipitates may have affected recrystallization during hot work, possibly by acting as strain localizers and thereby increasing the number of nucleation sites for recrystallization or by grain boundary pinning to hamper growth of recrystallized grains. Whether or not such a linearization of grain boundaries affects SCC crack propagation rates has not been treated in this work, but it is clear that an intergranular crack path would be locally less tortuous.
Observing the grain boundaries at high magnification in LOM revealed that the grain boundary carbides within the Ti(C,N) bands were coarse, which can be seen in Figure 6. In contrast, the parts of grain boundaries lying outside the banded regions were covered by fine carbides. Transitions from fine to coarse carbides in the middle of a grain boundary were observed, which shows that this observation was related to the banded region rather than the grain boundary misorientation. The same was observed on as-polished specimen in SEM using a BSE detector. This shows that the size difference is not an etching effect.
The microstructure of the DP bar is shown in Figure 7 and was the least homogeneous of the three investigated TT Alloy 690 materials. The microstructure was severely banded with small intragranular Ti(C,N) in the same way as the CRDM2 tube. The grains were coarser than in both the tube materials but were still equiaxed with plenty of fine carbides along the grain boundaries outside the banded regions. As in the CRDM2 tube, the grain boundary carbides within the banded regions were noticeably coarser. The tendency for reduced grain size in the banded regions was also observed in this material.
Unlike the CRDM2 tube, coarse M23C6 carbides of a significant amount were also present intragranularly in the banded regions. High magnification is required to differentiate M23C6 and Ti(C,N) in LOM. If the resolution is insufficient, both types of particles appear as dark spots which can lead to erroneous phase identification.
4.2. Heat Affected Zone
The HAZ of the Alloy 690 base metals from all three mockups showed a trend of M23C6 carbide dissolution close to the fusion line. Approaching the fusion line from the unaffected base metal, the carbide distribution changed from the initial semicontinuous network of fine M23C6 carbides into discrete and slightly coarser particles. Further approaching the fusion line, the M23C6 carbides were absent in LOM. Since the nital etchant is less effective in carbide-free grain boundaries in Alloy 690 , this region was only faintly etched. The apparently carbide-free zone typically spanned 100–500 μm wide depending on mockup. The full transition from unaffected grain boundary carbides to the full dissolution near the fusion line in the CRDM1 tube can be seen in Figure 8. Surprisingly, neither of the tube materials exhibited noticeable grain growth in the HAZ.
In the region where the grain boundary carbides appeared dissolved in LOM, only the occasional intergranular carbides could be seen in SEM, but only along some of the grain boundaries, and generally of very fine size. An example from the CRDM2 tube is shown in Figure 9(a), where the carbides are just barely visible, which can be compared with the grain boundary of the unaffected base metal at the same magnification shown in Figure 9(b). It is not clear if these carbides remained partially undissolved or if they were precipitated after the initial weld pass. Either way these carbides should not have experienced temperatures high enough for dissolution since the initial weld pass but have had the opportunity to grow due to the thermal cycles of the subsequent weld passes. In other words, they were likely to be both smaller and fewer during the weld induced straining of the initial weld pass. Thus, it is reasonable to believe that their presence was negligible, from a micromechanical point of view, during the straining.
The microstructure in the carbide-free region would have been similar to that of SA Alloy 690 during the weld induced straining. Since the plastic strains typically are the highest near the fusion line, it is possible that cold working Alloy 690 in the SA state yields a better representation of weld deformed HAZ than cold working it in the TT state. This may explain why SCC crack growth experiments on HAZ specimens have shown crack growth rates closer to specimens of Alloy 690 cold worked in the SA state than those cold worked in the TT state.
The previously mentioned coarser carbides in the bands of CRDM2 and DP appear to have been less affected by the weld. Compared to the carbides outside the bands, the coarser carbides within the bands appear to stay undissolved closer to the fusion line, as can be seen in Figure 10. Since a weld pass is a brief heat treatment, it is possible that slow kinetics did not permit a full dissolution of the coarser carbides. A large portion of the dissolved carbon would then have existing carbide surfaces to redeposit on during cooling or during the subsequent weld passes. Closer to the fusion line, however, even the coarsest of the carbide particles seem to have been fully dissolved.
Unlike the M23C6 carbides, the Ti(C,N) bands of CRDM2 and DP were not noticeably affected by the thermal cycles of the welding process, as can be seen in Figure 10. The Ti(C,N) precipitates remain, and in some cases the larger Ti(C,N) precipitates from the base metal could even be found in the weld metal. Even so, the weld induced strains did not cause cracked carbides or Ti(C,N) precipitates in the HAZ of any of the mockups, unlike in heavily cold rolled TT Alloy 690 where this type of damage is common [9, 10, 13].
4.3. Calculated Equilibrium Fractions and Composition of Phases
The thermodynamic calculations verify that the intragranular precipitates, usually referred to as TiN in the literature, in fact correspond to a carbonitride while in equilibrium with the matrix phase in solid state. The composition of the phase Ti(C,N) at 1000°C based on the alloy composition of the CRDM1 tube is shown in Table 3. The main dissolved element was found to be Cr (~0.6 mass-%) while Fe, Ni, Si, and Al were present only as trace quantities (10−6 mass-% or less). The solubility of Cr in Ti(C,N) increased slightly with temperature up to 0.9 mass-%, 2 mass-%, or 1 mass-% for alloys CRMD1, CRDM2, and DP, respectively. Otherwise, the composition of metallic elements in this phase was more or less constant.
However, the C/N ratio varied strongly with temperature, as shown in Figure 11. Note that the composition corresponds to TiN at temperatures where the matrix was fully molten, that is, where the TiN/Ti(C,N) phase was in equilibrium with the liquid phase. Note that this means that for all three Alloy 690 compositions, the Ti(C,N) phase was calculated to be fully dissolved only when above the temperature at which the matrix would be fully molten. This effect was most prominent for the CRDM1 alloy where the Ti(C,N) phase was fully dissolved at 1487°C, which is over 100 degrees higher than the calculated melting temperature of the matrix phase, that is, at 1381°C. Furthermore, according to the calculations the melting interval of the matrix phase was the same for all three compositions; see Figure 12.
The main differences between the mockup alloys were the total phase fractions of Ti(C,N) and the temperature at which Ti(C,N) was fully dissolved in the liquid. This means that a complete solid solution of all elements into the matrix is not possible for any of the investigated alloys, if the calculations are to be trusted. Thus any heat treatment performed at solid state temperatures, or at insufficient superheating above the melting temperature of the matrix, will leave a certain fraction of undissolved TiN/Ti(C,N) in the microstructure. Figure 12 also shows that little dissolution occurs at solid state temperatures, which means that the Ti(C,N) precipitates would remain essentially unaffected in the HAZ. These results are consistent with the observed microstructures near the fusion line (Figures 8 and 9), where the number of Ti(C,N) particles was still large while the M23C6 carbides were dissolved and did not notably reprecipitate during solidification after welding and the thermal cycles of subsequent weld passes. Furthermore, the higher phase fraction of Ti(C,N) in CRDM1 agrees well with the observations in LOM.
The temperature for full dissolution of the Cr-rich M23C6 phase was calculated to be 781°C for CRDM1. Only Fe and Ni were, to a small extent (~1-2 mass-%), dissolved in the carbide and the composition of this phase was more or less unaffected by the temperature. For the CRDM2 alloy, the dissolution temperature was calculated to be 983°C and for the DP alloy 889°C. Furthermore, the M23C6 carbide in CRDM2 also dissolved up to 4 mass-% Ni and 2.4 mass-% Fe and up to 9 mass-% Ni and 3.5 mass-% Fe in the DP alloy at higher temperatures.
A Cr-rich (95-96 mass-%) phase with body centered cubic (BCC) crystal structure was calculated to be stable below ~770–780°C for all three alloy compositions but was not observed in the samples. However, the M23C6 carbide was also stable in this temperature range and could be identified in the samples presented in Section 2. This could be due to the slower substitutional diffusion mechanism, which is required to form the BCC phase, while M23C6 may form locally by interstitial diffusion of C. Furthermore, the BCC phase could be difficult to find due to the low atomic number contrast when investigating the microstructure with SEM-BSE. On the other hand, to the best of the authors’ knowledge, the BCC phase has not been observed in Alloy 690 during any EBSD or transmission electron microscopy (TEM) studies either. It is therefore possible that the stability of this phase is overestimated in the thermodynamic database used.
Particle banding was observed in the TT Alloy 690 base metal of all three mockups investigated in this work. In samples from CRDM2 and DP, the bands consisted mainly of fine Ti(C,N) precipitates. In these samples the Ti(C,N) bands were associated with locally finer grain sizes and coarser intergranular carbides. Furthermore, the grain boundaries tended to line up along the bands, which reduced the intergranular path tortuosity in the materials’ respective longitudinal direction. The TT Alloy 690 samples from CRDM1 had the highest volume fraction of the Ti(C,N) phase but these particles were distributed as fewer large precipitates instead of many fine ones. In this material, the particle banding had negligible effects on the base metal microstructure.
The thermodynamic calculations showed that the equilibrium composition of the Ti(C,N) phase corresponds to TiN at temperatures where the matrix is fully molten. According to the calculations, the Ti(C,N) in the HAZ would remain essentially unaffected by the heat from welding, which is verified by the observed microstructure near the fusion line. The calculations also indicated stability of a Cr-rich BCC phase below roughly 770–780°C, which so far has not been verified experimentally and could therefore be an artifact.
The main welding induced microstructural change was the full dissolution of intergranular M23C6 carbides near the fusion line. The width of the carbide-free region varied greatly between mockups, ranging roughly between 100 and 500 μm in this work. The transition region with partially dissolved carbides was of comparable width as the carbide-free region. In this transition region, the coarser carbides located within the Ti(C,N) bands appeared less affected by the weld. No cracked M23C6 carbides or Ti(C,N) precipitates were observed as a result of welding induced straining.
Since the weld induced plastic straining takes place during cooling after the carbide dissolution, cold worked SA Alloy 690 would be a better representation of this region than cold worked TT Alloy 690. This fits well with the SCC crack growth rates reported in the literature.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
This work has been performed under the financial support of the energy companies Vattenfall, Fortum, and Eon. The authors would also like to acknowledge EPRI and Ringhals AB for providing the mockups.
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