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Hydrogen embrittlement in power plant steels - Indian Academy of ...

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<strong>Hydrogen</strong> <strong>embrittlement</strong> <strong>in</strong> <strong>power</strong> <strong>plant</strong> <strong>steels</strong> 437<br />

diffuses will is proportional to the triaxial component <strong>of</strong> the stress. At temperatures below<br />

about 200 ◦ C, the diffusion is h<strong>in</strong>dered by the ‘traps’ (sites <strong>in</strong> metal matrix) which capture and<br />

delay migrat<strong>in</strong>g hydrogen atoms.<br />

3.2 Location <strong>of</strong> critical hydrogen <strong>in</strong>teraction<br />

There are several specific locations <strong>in</strong> a material where the presence <strong>of</strong> hydrogen may be<br />

critical to the fracture behaviour. These <strong>in</strong>clude the lattice itself (hydrogen <strong>in</strong> solution) as<br />

well as gra<strong>in</strong> boundaries, <strong>in</strong>coherent and coherent precipitates, voids and dislocations as<br />

shown <strong>in</strong> figure 10 (Thompson & Bernste<strong>in</strong> 1980). The figure <strong>in</strong>dicates the way <strong>in</strong> which<br />

hydrogen from a variety <strong>of</strong> sources transported by dislocations or lattice diffusion can accumulate<br />

at any one or jo<strong>in</strong>tly with other sites (traps) <strong>in</strong> the metal matrix. These traps are<br />

classified as ‘irreversible’ if they act purely as hydrogen s<strong>in</strong>ks or reversible if they accept<br />

hydrogen under some circumstances but act as a hydrogen source otherwise. The so-called<br />

irreversible traps liberate hydrogen at a sufficiently elevated temperature which depends on<br />

the trap energy (Davidson 1995). The local hydrogen concentration at a potential crack site<br />

must reach a critical level for a given stress <strong>in</strong>tensity factor (K I ) before the <strong>in</strong>itiation <strong>of</strong><br />

crack<strong>in</strong>g. The hydrogen traps <strong>in</strong>fluence the likelihood <strong>of</strong> crack<strong>in</strong>g by controll<strong>in</strong>g the availability<br />

<strong>of</strong> hydrogen to the critical crack<strong>in</strong>g locations. The effect <strong>of</strong> hydrogen trapp<strong>in</strong>g on the<br />

diffusivity <strong>of</strong> hydrogen is shown <strong>in</strong> figure 11 (Yurioka & Sazuki 1990) where the apparent<br />

diffusion coefficient is shown as a function <strong>of</strong> temperature. An <strong>in</strong>crease <strong>in</strong> temperature<br />

decreases the trap energy, thus decreas<strong>in</strong>g their tendency to h<strong>in</strong>der hydrogen diffusion. Above<br />

about 400 ◦ C, the apparent diffusion coefficient is close to the diffusion coefficient <strong>of</strong> hydrogen<br />

by lattice diffusion while below this temperature the diffusion coefficient is affected<br />

by hydrogen trapp<strong>in</strong>g. The number <strong>of</strong> reversible traps is strongly affected by the transformation<br />

products formed on cool<strong>in</strong>g. For example a tempered martensite has more trapp<strong>in</strong>g<br />

sites than a pearlite. This is due to the <strong>in</strong>creased surface area <strong>of</strong> the f<strong>in</strong>er carbides <strong>in</strong> the<br />

martensite.<br />

(a) (b) (c)<br />

(d) (e) (f)<br />

Figure 10. Schematic view <strong>of</strong><br />

dest<strong>in</strong>ations for hydrogen <strong>in</strong> a<br />

metal microstructure: (a) solid<br />

solution; (b) solute–hydrogen<br />

pair; (c) dislocation atmosphere;<br />

(d) gra<strong>in</strong> boundary accumulation;<br />

(e) particle-matrix <strong>in</strong>terface<br />

accumulation; (f) void conta<strong>in</strong><strong>in</strong>g<br />

recomb<strong>in</strong>ed hydrogen (Thompson<br />

& Bernste<strong>in</strong> 1980).

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