C. R. Hills

Bio: C. R. Hills is an academic researcher from Sandia National Laboratories. The author has contributed to research in topics: Martensite & Austenite. The author has an hindex of 3, co-authored 4 publications receiving 199 citations.

Microstructural evolution of modified 9Cr-1Mo steel

Abstract: The tempering and subsequent annealing of modified 9Cr-lMo steel have been investigated to determine the influence of trace amounts of V and Nb on the sequence of precipitation processes and to identify the basis for the enhanced high-temperature strength compared to the standard 9Cr-lMo composition. Air cooling (normalizing) from 1045 °C results in the precipitation of fine (Fe, Cr)3C particles within the martensite laths. Additional carbide precipitation and changes in the dislocation structure occur during the tempering of martensite at 700 °C and 760 °C after normalizing. The precipitation of M23C6 carbides occurs preferentially at lath interfaces and dislocations. The formation of Cr2C was detected during the first hour of tempering over the range of 650 °C to 760 °C but was replaced by V4C3 within 1 hour at 760 °C. During prolonged annealing at 550 °C to 650 °C, following tempering, the lath morphology remains relatively stable; partitioning of the laths into subgrains and some carbide coarsening are evident after 400 hours of annealing at 650 °C, but the lath morphology persists. The enhanced martensite lath stability is attributed primarily to the V4C3 precipitates distributed along the lath interfaces and is suggested as the basis for the improved performance of the modified 9Cr-lMo alloy under elevated temperature tensile and creep conditions.

The influence of palladium on the hydrogen-assisted cracking resistance of PH 13-8 Mo stainless steel

Abstract: We compare the hydrogen-assisted cracking resistance of wrought PH 13-8 Mo stainless steel alloyed with 0.4 to 1.0 wt pct palladium to the conventional alloy when aged to yield strengths of 1170 to 1250 MPa. Intergranular hydrogen cracking is suppressed with Pd in both static load and constant extension rate tests conducted with electrochemical hydrogen charging. These results are analyzed to elucidate the role of Pd in suppressing intergranular cracking. Palladium is found both in substitutional solid solution in the martensitic phase and also in the form of randomly distributed PdAl precipitates in all Pd-modified alloys. Interfacial segregation of Pd to grain boundaries and lath boundaries is not observed at any levels above a detection limit of approximately 0.5 monolayers. Hydrogen permeation analyses indicate that hydrogen ingress is not inhibited by Pd but that apparent diffusion coefficients are lowered relative to the conventional alloy. Lower diffusion coefficients are consistent with the creation of a strong but reversible hydrogen trap, identified as the uniformly distributed PdAl phase. We hypothesize that PdAl trap sites force a redistribution of trapped hydrogen, which lowers the amount of interfacially segregated hydrogen at prior austenite grain boundaries for the electrochemical conditions applied. These assertions are supported by a simplistic trapping model for PH 13-8 Mo which shows that both the hydrogen trap binding energy and the trap density for the PdAl trapping site are greater than the hydrogen trap binding energy and density for prior austenite grain boundaries.

An investigation of the high-temperature and solidification microstructures of PH 13-8 Mo stainless steel

Abstract: Differential thermal analysis (DTA), high-temperature water-quench (WQ) experiments, and optical and electron microscopy were used to establish the near-solidus and solidification microstructures in PH 13-8 Mo. On heating at a rate of 0. 33 °C/s, this alloy begins to transform from austenite to δ-ferrite at ≈1350 °C. Transformation is complete by ≈1435 °C. The solidus is reached at ≈1447 °C, and the liquidus is ≈1493 °C. On cooling from the liquid state at a rate of 0. 33 °C/s, solidification is completed as δ-ferrite with subsequent transformation to austenite beginning in the solid state at ≈1364 °C. Insufficient time at temperature is available for complete transformation and the resulting room-temperature microstructure consists of matrix martensite (derived from the shear decomposition of the austenite) and residual δ-ferrite. The residual δ-ferrite in the DTA sample is enriched in Cr (≈16 wt pct), Mo (≈4 wt pct), and Al (≈1. 5 wt pct) and depleted in Ni (≈4 wt pct) relative to the martensite (≈12. 5 wt pct Cr, ≈2 wt pct Mo, ≈1 wt pct Al, ≈9 wt pct Ni). Solid-state transformation of δσ γ was found to be quench-rate sensitive with large grain, fully ferritic microstructures undergoing a massive transformation as a result of water quenching, while a diffusionally controlled Widmanstatten structure was produced in air-cooled samples.

The Partitioning of Alloying Elements in Vacuum Arc Remelted, Pd-Modified PH 13-8 Mo Alloys

Abstract: The partitioning of alloying elements in as-solidified PH 13-8 Mo stainless steel containing up to 1.02 wt pct Pd has been investigated. The as-solidified structure is composed of two major phases, martensite and ferrite. Electron probe microanalysis reveals that Mo, Cr, and Al partition to the ferrite phase while Fe, Ni, Mn, and Pd partition to the martensite (prior austenite) during solidification and cooling from the solidus. In addition to bulk segregation between phases, precipitation of the intermetallic, PdAI, in the retained ferrite is observed. Precipitation of the normal hardening phase, β-NiAl, is also observed in the retained ferrite. Partition ratios of the various alloying elements are determined and are compared with those observed previously in duplex Fe-Cr-Ni stainless steel solidification structures. The martensite start temperature (Ms) was observed to decrease with increasing Pd concentration.

Hydrogen-enhanced-plasticity mediated decohesion for hydrogen-induced intergranular and “quasi-cleavage” fracture of lath martensitic steels

Abstract: Hydrogen embrittlement of lath martenistic steels is characterized by intergranular and “quasi-cleavage” transgranular fracture. Recent transmission electron microscopy (TEM) analyses (Nagao et al., 2012a, 2014a, 2014b, 2014c) of samples lifted from beneath fracture surfaces through focused ion beam machining (FIB) revealed a failure mechanism that can be termed hydrogen-enhanced-plasticity mediated decohesion. Fracture occurs by the synergistic action of the hydrogen-enhanced localized plasticity and decohesion. In particular, intergranular cracking takes place by dislocation pile-ups impinging on prior austenite grain boundaries and “quasi-cleavage” is the case when dislocation pile-ups impinge on block boundaries. These high-angle boundaries, which have already weakened by the presence of hydrogen, debond by the pile-up stresses. The micromechanical model of Novak et al. (2010) is used to quantitatively describe and predict the hydrogen-induced failure of these steels. The model predictions verify that introduction of nanosized (Ti,Mo)C precipitates in the steel microstructure enhances the resistance to hydrogen embrittlement. The results are used to discuss microstructural designs that are less susceptible to hydrogen-induced failure in systems with fixed hydrogen content (closed systems).

Hydrogen Assisted Cracking of High Strength Alloys

Abstract: : Two important advances over the past 40 years enable the optimization and management of the structural integrity of components in high performance applications. First, the solid mechanics conununity established linear elastic fracture mechanics as the premier framework for modeling the damage tolerance of fracture critical components (Irwin and Wells, 1997; Paris, 1998). Second, materials scientists developed metals with outstanding balances of high tensile strength and high fracture toughness (Garrison, 1990; Wells, 1993; Boyer, 1993; Starke and Staley, 1995; Olson, 1997; Kolts, 1996). An example of achievable strength-toughness properties is provided in Fig. 1, a plot of plane strain fracture toughness vs. tensile yield strength (sigma-YS) for ultra-high strength steels (UHSS) and beta-Ti alloys precipitation hardened with a phase (Gangloff 2001). New nano-scale characterization and high performance computational methods provide for additional advances in the mechanical performance properties of structural metals. These modem alloys and analysis tools satisfy technological needs for optimization and management of component performance in demanding fatigue and fracture critical applications in the aerospace, marine, energy, transportation, and defense sectors.

Characterization of Microstructures across the Heat-Affected Zone of the Modified 9Cr-1Mo Weld Joint to Understand Its Role in Promoting Type IV Cracking

Abstract: In the postweld heat-treated (PWHT) fusion welded modified 9Cr-1Mo steel joint, a soft zone was identified at the outer edge of the heat-affected zone (HAZ) of the base metal adjacent to the deposited weld metal. Hardness and tensile tests were performed on the base metal subjected to soaking for 5 minutes at temperatures below Ac1 to above Ac3 and tempering at the PWHT condition. These tests indicated that the soft zone in the weld joint corresponds to the intercritical region of HAZ. Creep tests were conducted on the base metal and cross weld joint. At relatively lower stresses and higher test temperatures, the weld joint possessed lower creep rupture life than the base metal, and the difference in creep rupture life increased with the decrease in stress and increase in temperature. Preferential accumulation of creep deformation coupled with extensive creep cavitation in the intercritical region of HAZ led to the premature failure of the weld joint in the intercritical region of the HAZ, commonly known as type IV cracking. The microstructures across the HAZ of the weld joint have been characterized to understand the role of microstructure in promoting type IV cracking. Strength reduction in the intercritical HAZ of the joint resulted from the combined effects of coarsening of dislocation substructures and precipitates. Constrained deformation of the soft intercritical HAZ sandwich between relatively stronger constitutes of the joint induced creep cavitation in the soft zone resulting in premature failure.

Hydrogen trap states in ultrahigh-strength AERMET 100 steel

Abstract: Hydrogen (H) trap states and binding energies were determined for AERMET 100 (Fe-13.4Co-11Ni-3Cr-1.2Mo-0.2C), an ultrahigh-strength steel using thermal desorption methods. Three major H desorption peaks were identified in the precipitation-hardened microstructure, associated with three distinct metallurgical trap states, and apparent activation energies for desorption were determined for each. The lattice diffusivity (D L ) associated with interstitial H was measured experimentally and verified through trapping theory to yield H-trap binding energies (E b ). Solid-solution elements in AERMET 100 reduce D L by decreasing the pre-exponential diffusion coefficient, while the activation energy for migration is similar to that of pure iron. M2C precipitates are the major reversible trap states, with E b of 11.4 to 11.6 kJ/mol and confirmed by heat treatment that eliminated these precipitates and the associated H-desorption peak. A strong trap state with E b of 61.3 to 62.2 kJ/mol is likely associated with martensite interfaces, austenite grain boundaries, and mixed dislocation cores. Undissolved metal carbides and highly misoriented grain boundaries trap H with a binding energy of 89.1 to 89.9 kJ/mol. Severe transgranular hydrogen embrittlement in peak-aged AERMET 100 at a low threshold-stress intensity is due to H repartitioning from a high density of homogeneously distributed and reversible M2C traps to the crack tip under the influence of high hydrostatic tensile stress.