Role of residual stresses induced by industrial fabrication on stress corrosion cracking susceptibility of austenitic stainless steel

Effect of residual stress generated during tube fabrication, roll expansion and machining of stainless steel on the stress corrosion cracking (SCC) susceptibility was studied by testing fabricated tubes, tube–tube sheet joint and heavily machined plate of austenitic stainless steel (SS) in boiling MgCl₂. U bend samples of machined plate were exposed to acidified SO₄ + Cl^? environment at room temperature to study its ambient temperature SCC behavior. The results correlate the SCC behavior of the SS tubes and roll expanded joints to the nature and magnitude of residual stresses present. The study also highlights the distinct difference in ambient temperature SCC behavior of machined vs. nonmachined surfaces.     

Effect of graft copolymerization of mixtures of acrylamide and methyl methacrylate on mechanical properties of jute fibers of different compositions

The role of persulfate-induced graft copolymerization of mixtures of acrylamide and methyl methacrylate at 50°C in modifying mechanical properties of jute fibers of different compositions was studied in a limited aqueous system following a pretreatment technique. Results obtained indicate that such a process admits a good scope for modification of mechanical properties of jute fiber depending on degree of grafting achieved and compositional variations of (1) the feed monomer mixture and (2) the multiconstituent jute itself, consequent to selective removal of lignin and hemicellulose to different extents from the fiber. Low to moderate removal of hemicellulose is more effective than a similar degree of removal of lignin from jute in rendering the fiber more amenable to vinyl grafting using the mixed monomer system without being adversely affected with respect to tensile properties. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 1139–1147, 1998     

Fusion Multistyle Training for Speaker Identification of Disguised Speech

Wireless Personal Communications - Determining the speaker of a given speech utterance from a group of people is referred to as speaker identification. When voice disguising is done by a person,...     

Revisiting the mechanism of the triosephosphate isomerase reaction: the role of the fully conserved glutamic acid 97 residue

An analysis of 503 available triosephosphate isomerase sequences revealed nine fully conserved residues. Of these, four residues—K12, H95, E97 and E165—are capable of proton transfer and are all arrayed around the dihydroxyacetone phosphate substrate in the three‐dimensional structure. Specific roles have been assigned to the residues K12, H95 and E165, but the nature of the involvement of E97 has not been established. Kinetic and structural characterization is reported for the E97Q and E97D mutants of Plasmodium falciparum triosephosphate isomerase (Pf TIM). A 4000‐fold reduction in k_cat is observed for E97Q, whereas the E97D mutant shows a 100‐fold reduction. The control mutant, E165A, which lacks the key catalytic base, shows an approximately 9000‐fold drop in activity. The integrity of the overall fold and stability of the dimeric structure have been demonstrated by biophysical studies. Crystal structures of E97Q and E97D mutants have been determined at 2.0 Å resolution. In the case of the isosteric replacement of glutamic acid by glutamine in the E97Q mutant a large conformational change for the critical K12 side chain is observed, corresponding to a trans‐to‐gauche transition about the Cγ? Cδ (χ³) bond. In the E97D mutant, the K12 side chain maintains the wild‐type orientation, but the hydrogen bond between K12 and D97 is lost. The results are interpreted as a direct role for E97 in the catalytic proton transfer cycle. The proposed mechanism eliminates the need to invoke the formation of the energetically unfavourable imidazolate anion at H95, a key feature of the classical mechanism.     

SiC–YAG sintered composites from hydroxy hydrogel powder precursors

Yttrium hydroxide and aluminium hydroxide hydrogel were derived from yttrium nitrate and aluminium nitrate through hydroxy hydrogel route in which SiC particles were kept dispersed. The gel-like mass was heat treated at 900°C in ambient atmosphere followed by heat treatment at 1400°C in Ar atmosphere. The specimens were then sintered in the temperature range of 1800–1950°C in Ar atmosphere with 30 min soaking. The phases were identified by XRD analysis. Microstructure of the sintered materials were analysed by scanning electron micrograph. With this new method of preparation of powder precursors, the process of sintering was easier and almost theoretical density was achieved with moderate hardness. The mechanism of densification was postulated to be a solid-state initiated liquid phase sintering and the overall process of which was activated by the reactive species formed from hydroxy hydrogel powder precursors.