Optical study of poly(vinyl alcohol)/hydroxypropyl methylcellulose blends

The proposal in this study was to evaluate the optical properties of different biopolymers films. The materials used were poly(vinyl alcohol) (PVA) and hydroxypropyl methylcellulose (HPMC). PVA/HPMC blends were prepared by casting technique. Variations in the group coordination in the infrared region were followed. The effects of HPMC concentrations on the optical properties of the PVA films were studied by near infrared, ultraviolet/visible, transmittance, and reflectance in the spectral region 200–2500 nm. Absorption, transmittance, and reflectance spectra were used for the determination of the optical constants. The study has been also extended to include the changes in the optical parameters including the band tail width and band gap energies and extinction coefficient for the investigated films. The results indicate that the optical band gap was derived from Tauc’s extrapolation and decreases with the HPMC contents. The obtained optical parameters were found to be strongly affected by HPMC contents.     

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A process for the recovery of uranium, vanadium and fluorine as byproducts of phosphoric acid obtained via hydrochloric acid (the cheapest locally produced acid) acidulation of phosphate ores was studied. At a redox potential of 180–200 mV, by introducing iron powder into the leaching circuit at 90°C, a relatively small amount of uranium and vanadium residue was obtained. The residue obtained was roasted with sodium chloride at 850°C to produce water-soluble sodium vanadate. Water leaching then removed the vanadium, leaving a uranium residue. The uranium was selectively leached by sodium carbonate at a redox potential of 480 mV. The product was then processed by alkaline decomposition to prepare the sodium diuranate concentrate necessary for uranium processing. Fluorine was recovered during the acid leaching process as sodium fluorosilicate by adding a stoichiometric amount of rock salt or sodium carbonate to the leaching circuit.     

Neurobehavioral tests as a medical surveillance procedure: applying evaluative criteria

Neurobehavioral impairment is among the earliest indicators of a toxic insult on the nervous system. Neurobehavioral tests measure behavior impairment by noninvasive procedures that assess various performance and personality changes. Neurobehavioral tests have been used on groups of workers included in epidemiologic research studies; however, their suitability for an ongoing medical surveillance program for workers exposed to neurotoxic agents has not been evaluated. In Ontario, Canada, a set of validity criteria must be met to determine whether a medical procedure may be prescribed for a specific medical surveillance program. The evaluative criteria are standards for judging the desirability of a procedure based on social values and scientific considerations. In this paper, various studies using neurobehavioral tests are reviewed, and the validity of using these procedures for medical surveillance is evaluated by applying the Ontario evaluation criteria. The conclusion is that neurobehavioral tests are useful for well-controlled, cross-sectional studies, but they do not yet meet the validity criteria for procedures prescribed in an ongoing medical surveillance program for workers exposed to neurotoxic agents.     

Effekt of Using a Starter Culture Grown on Soy Milk Medium on some Properties of “Ras” Cheese

Ras cheese was manufactured using a starter culture grown on soy milk medium. Resultant cheese was compared with that resulted by using the ordinary starter culture grown on skim milk medium. The use of the former starter resulted in increasing cheese acidity, total volatile fatty acids, formol and SCHILOVICH ripening indices throughout the ripening period. Also higher total bacterial number and lactic acid bacterial number were observed.     

Cholesterol-dependent human complement activation resulting in damage to liposomal model membranes

Human (but not guinea pig) complement-mediated damage. It was concluded that human complement was activated spontaneously by liposomes containing a high concentration (71 mol %) of cholesterol. This occurred in the absence of any recognizable antigen or antibody, and did not occur at a low concentration (43 mol %) of cholesterol. Activation of complement resulted in membrane damage and release of trapped liposomal glucose. The complement activity was inhibited by preheating (56 degrees C, 30 min), 10 mM Mg2EDTA3 or EGTA, and by prior adsorption with insoluble immune complexes. Almost all human sera had some reactivity, but it ranged from very low levels (less than 7% liposomal glucose release) to very high levels (greater than 50% glucose release). Complement activation appeared to be mediated by a serum factor which could be removed by adsorption and which was partially heat labile. The factor was transferred by adding heated high reacting human serum to unheated low reacting human serum, or to guinea pig serum. The serum factor, although quantitatively diminished in potency due to heat lability, caused equal activation of each of these two latter complement sources in the presence of high cholesterol liposomes. It did not cause activation of C4-deficient guinea pig complement. These data suggested that the classical complement pathway was activated. The liposomal membrane composition had an influence on this phenomenon. Activities of about half of the human sera were enhanced when galactosyl ceramide, or ceramide alone, was present in the liposomes. Activity was enhanced by longer fatty acyl chain lengths of lecithin when dimyristoyl-, dipalmitoyl-, or distearoyllecithin was employed in the liposomes. Liposomes containing sphingomyelin as the only phospholipid were not sensitive to cholesterol-dependent complement-mediated damage. It was concluded that human complement was activated in the presence of high concentrations of membrane cholesterol and that this was caused by an uncharacterized serum factor and was influenced by the lipid composition of the membrane.     

Multi-objective topology optimization of multi-component continuum structures via a Kriging-interpolated level set approach

This paper explores a framework for topology optimization of multi-component sheet metal structures, such as those often used in the automotive industry. The primary reason for having multiple components in a structure is to reduce the manufacturing cost, which can become prohibitively expensive otherwise. Having a multi-component structure necessitates re-joining, which often comes at sacrifices in the assembly cost, weight and structural performance. The problem of designing a multi-component structure is thus posed in a multi-objective framework. Approaches to solve the problem may be classified into single and two stage approaches. Two-stage approaches start by focusing solely on structural performance in order to obtain optimal monolithic (single piece) designs, and then the decomposition into multiple components is considered without changing the base topology (identical to the monolithic design). Single-stage approaches simultaneously attempt to optimize both the base topology and its decomposition. Decomposition is an inherently discrete problem, and as such, non-gradient methods are needed for single-stage and second stage of two-stage approaches. This paper adopts an implicit formulation (level-sets) of the design variables, which significantly reduces the number of design variables needed in either single or two stage approaches. The number of design variables in the formulation is independent from the meshing size, which enables application of non-gradient methods to realistic designs. Test results of a short cantilever and an L-shaped bracket studies show reasonable success of both single and two stage approaches, with each approach having different merits.     

Asymmetrical hemispheric activation and behavioral persistence: effects of unilateral muscle contractions

OBJECTIVE: To compare pubertal maturation, sex steroid hormones, and lipoproteins and their interrelationships in male offspring of parents with premature coronary heart disease (cases) and a control group. DESIGN: This was a cross-sectional comparison of cases and members of a control group 10 to 15 years of age. SUBJECTS AND METHODS: Offspring were recruited from patient lists of area physicians. Members of the control group were recruited from area schools. Body mass (kg/m2), serum lipids, lipoproteins, apolipoproteins, estradiol, and free testosterone were measured. RESULTS: Differences in age were not significant, but offspring were taller, heavier, and more mature. Offspring had higher total and low density lipoprotein cholesterol. Offspring had lower estradiol levels in early puberty but higher levels in late puberty. With family history and body mass in the regression models for lipid parameters, free testosterone was a significant explanatory factor for total cholesterol, low-density lipoprotein cholesterol, and high-density lipoprotein, and estradiol was a significant predictor for apolipoprotein B. The percent of the variance in the lipid parameters explained by testosterone and estradiol was small. CONCLUSION: Sex hormone concentrations appear to be modest but significant predictors of lipoprotein and apolipoprotein concentrations in offspring and a control group in cross-sectional analysis. After controlling for pubertal maturation, hormone and lipid concentrations differed in offspring and the control group.