The influence of stacking fault energy on ductile fracture micromorphology

The influence of stacking fault energy on microvoid coalescence in pure materials has been studied. It was shown that as a material's stacking fault energy (SFE) decreased, the extent of microvoid coalescence that occurred during ductile fracture also decreased. The decrease of microvoid coalescence in low SFE materials was attributed to a hindrance in the development of dislocation cells associated with the restricted motion of dislocations. In pure materials, microvoids are believed to initiate and grow along dislocation cell walls formed during deformation. As such, the absence or scarcity of cells in lower SFE materials limits the formation of these voids during ductile fracture.     

Oxidation of Hydrogen Sulfide by Quinones: How Polyphenols Initiate Their Cytoprotective Effects

We have shown that autoxidized polyphenolic nutraceuticals oxidize H₂S to polysulfides and thiosulfate and this may convey their cytoprotective effects. Polyphenol reactivity is largely attributed to the B ring, which is usually a form of hydroxyquinone (HQ). Here, we examine the effects of HQs on sulfur metabolism using H₂S- and polysulfide-specific fluorophores (AzMC and SSP4, respectively) and thiosulfate sensitive silver nanoparticles (AgNP). In buffer, 1,4-dihydroxybenzene (1,4-DB), 1,4-benzoquinone (1,4-BQ), pyrogallol (PG) and gallic acid (GA) oxidized H₂S to polysulfides and thiosulfate, whereas 1,2-DB, 1,3-DB, 1,2-dihydroxy,3,4-benzoquinone and shikimic acid did not. In addition, 1,4-DB, 1,4-BQ, PG and GA also increased polysulfide production in HEK293 cells. In buffer, H₂S oxidation by 1,4-DB was oxygen-dependent, partially inhibited by tempol and trolox, and absorbance spectra were consistent with redox cycling between HQ autoxidation and H₂S-mediated reduction. Neither 1,2-DB, 1,3-DB, 1,4-DB nor 1,4-BQ reduced polysulfides to H₂S in either 21% or 0% oxygen. Epinephrine and norepinephrine also oxidized H₂S to polysulfides and thiosulfate; dopamine and tyrosine were ineffective. Polyphenones were also examined, but only 2,5-dihydroxy- and 2,3,4-trihydroxybenzophenones oxidized H₂S. These results show that H₂S is readily oxidized by specific hydroxyquinones and quinones, most likely through the formation of a semiquinone radical intermediate derived from either reaction of oxygen with the reduced quinones, or from direct reaction between H₂S and quinones. We propose that polysulfide production by these reactions contributes to the health-promoting benefits of polyphenolic nutraceuticals.     

The Effect of Cadmium on GFR Is Clarified by Normalization of Excretion Rates to Creatinine Clearance

Erroneous conclusions may result from normalization of urine cadmium and N-acetyl-β-D-glucosaminidase concentrations ([Cd]_u and [NAG]_u) to the urine creatinine concentration ([cr]_u). In theory, the sources of these errors are nullified by normalization of excretion rates (E_Cd and E_NAG) to creatinine clearance (C_cr). We hypothesized that this alternate approach would clarify the contribution of Cd-induced tubular injury to nephron loss. We studied 931 Thai subjects with a wide range of environmental Cd exposure. For x = Cd or NAG, E_x/E_cr and E_x/C_cr were calculated as [x]_u/[cr]_u and [x]_u[cr]_p/[cr]_u, respectively. Glomerular filtration rate (GFR) was estimated according to the Chronic Kidney Disease (CKD) Epidemiology Collaboration (eGFR), and CKD was defined as eGFR < 60 mL/min/1.73m². In multivariable logistic regression analyses, prevalence odds ratios (PORs) for CKD were higher for log(E_Cd/C_cr) and log(E_NAG/C_cr) than for log(E_Cd/E_cr) and log(E_NAG/E_cr). Doubling of E_Cd/C_cr and E_NAG/C_cr increased POR by 132% and 168%; doubling of E_Cd/E_cr and E_NAG/E_cr increased POR by 64% and 54%. As log(E_Cd/C_cr) rose, associations of eGFR with log(E_Cd/C_cr) and log(E_NAG/C_cr) became stronger, while associations of eGFR with log(E_Cd/E_cr) and log(E_NAG/E_cr) became insignificant. In univariate regressions of eGFR on each of these logarithmic variables, R² was consistently higher with normalization to C_cr. Our tabular and graphic analyses uniformly indicate that normalization to C_cr clarified relationships of E_Cd and E_NAG to eGFR.     

Current-Source Converter for AC Motor Drives

The employment of current-source concepts in thyristor converters to obtain adjustable frequency and adjustable current waveforms is presented. The use of a dc filter choke and a current feedback loop to produce a regenerative current source is explained. The simplified inverter commutation circuit made possible by the current-source technique is also discussed. Finally, a brief review of the inherently rugged current-source converter's ability to provide wide range control of an ac induction motor is given.     

A kinetic study of the adsorption and desorption process of two commercial molecular sieves

A mathematical model and its numerical solution is presented to describe adiabatic adsorption—desorption processes in a fixed bed when the mass and heat transfer can be described by external film transfer coefficients only, which is especially interesting in the case of non-uniform, irregular particles. A new method to measure such rates is presented, based on continuous weighing of a through-circulated bed. The measured rates can be checked against the difference in humidity and temperature between the outlet and inlet air in order to minimize errors.The comparison between experimental results and calculations showed that the adsorption process in a bed of molecular sieve pellets can not be described with a constant mass transfer coefficient; the desorption process is better described although not entirely satisfactorily. In the case of a honeycomb molecular sieve, a constant mass transfer coefficient described both the adsorption and desorption processes satisfactorily.     

Compound types and properties of Utah and Athabasca tar sand bitumens

Properties and compound types were examined in detail for tar-sand bitumens representative of four major deposits in Utah and Alberta. Methods for bitumen extraction, separation, and compound type (functional group) analysis are presented. Results of the analyses are compared with each other and with results in the literature for tar-sand bitumens and petroleum. Comparison of the results of Utah bitumens with the Athabasca bitumen provides a basis for evaluation of the Utah bitumens because considerable information about the processing characteristics of the Athabasca bitumen has been reported. Simulated distillation and Chromatographic separation data indicate that, in general, the tarsand bitumens most closely resemble Wilmington petroleum with respect to hydrocarbon/non-hydrocarbon distribution, especially in the non-distilling portion (the distillable portions, mainly hydrocarbons, are similar for all samples). Tar-sand bitumens were also shown to differ significantly from one another, principally in the amounts and kinds of heteroatomic compound types present. This information is important because of the effects that composition has on recovery and refining processes. Analyses of the chemical functionalities also provide a basis for developing correlations between bitumen composition and the recovery and processing characteristics of the bitumen.     

Allelopathic polyacetylenes fromCentaurea repens (Russian knapweed)

The allelopathic weed Russian knapweed (Centaurea repens) was found to contain polyacetylenes VIII–XIV in the roots. Dose vs. response of the root length elongation against lettuce, alfalfa, barnyard grass, and red millet showed IX to be active. Closely related isomers were not active. Examination of the soil surrounding the Russian knapweed roots revealed the presence of IX in sufficient concentration to have an appreciable effect on the surrounding plant community.     

Laboratory study of air-water-coal combustion product (fly ash and FGD solid) mercury exchange

Recent laboratory research has indicated that coal fly ash derived from subbituminous and bituminous type coals is a sink for atmospheric mercury (Hg), however lignite-based ash was found to emit Hg to the air. Solids collected from systems with components that enhance Hg removal (i.e. activated carbon injection (ACI), flue gas desulfurization (FGD), and selective catalytic reduction (SCR) or selective non-catalytic reduction (SNCR)) may have higher Hg concentrations and therefore a higher potential for Hg release. For this study we investigated the potential for Hg release to the air and water from coal combustion products (CCPs) collected from coal-fired units with FGD equipment, SCR and SNCR equipment, and sorbent injection for Hg removal. In the laboratory study, most dry samples acted as sinks for atmospheric Hg in the dark at 25 °C. When exposed to light or increased temperature (45 °C), deposition of Hg to the fly ash substrates in most cases continued but decreased. Wet FGD samples emitted Hg. However, they became a sink for atmospheric Hg or exhibited low Hg emission rates when dried. Mercury flux in the dark at 25 °C was correlated with fly ash carbon content (LOI). Most liquid extracts derived using the synthetic precipitation leaching procedure (SPLP EPA method 1312) had very low Hg concentrations (<13 ng/l).     

Measurement of Crack Tip Displacement Fields in Mixed Mode I–Mode III Fracture

A new method has been devised to propagate stable subcritical mixed mode I–mode III cracks in soda–lime–silicate and borosilicate glasses. The mode I content was measured using an original optical tunneling technique and mode III content via multiple-beam interferometry. Measurement of the mode III displacement field allows values of mode III fracture toughness, K_III, to be derived. K_III vs crack velocity (v) diagrams have been constructed for both glasses, and, in the case of the soda–lime–silicate glass, v vs K_III relationships have been determined for a variety of humidities. Comparison has been made with published K_I vs v data for this glass.     

Kinetics of droplet growth in liquid—liquid phase separation of polymer—diluent systems: experimental results

Liquid—liquid thermally induced phase separation of the polymer—diluent system isotactic poly(propylene)—diphenyl ether was studied under an optical microscope. It was found that as the system phase separated, droplets of a diluent-rich phase formed within a polymer-rich matrix. These droplets grew in size and decreased in number by a process known as coarsening. The scaling exponent relating droplet diameter and time was determined. The scaling exponent was found to be a strong function of the droplet phase volume fraction, and this strong dependence on volume fraction was relatively insensitive to temperature. The influence of the ratio of interfacial tension between the phases and the viscosity of the matrix phase was less significant on the growth rate of the droplets.