The reuse of reactive dye liquors using charged ultrafiltration membrane technology

A closed-loop recycle system using a charged ultrafiltration membrane to decolourise reactive dye effluents from a textile yarn and fabric dyeing process is described. The economics of the process depend on the value of the electrolyte ($5 to $10 per M³). Conventional reactive dyeing technology was examined and modified to facilitate dye liquor reuse. The performance of the membrane was examined in terms of electrolyte rejection, colour rejection and permeate flux under varying conditions of solution pH, ionic strength and operating pressure.     

Sorption of Aniline by Montmorillonite

Sorption of aniline by montmorillonite was studied by infra-red, X-ray diffraction and differential thermal analysis methods. The amount of aniline sorbed and the type of bonding depend upon the interlayer cations: anilinium, H⁺- and Al³⁺- give anilinium aniline ions, NH₄⁴-ammonium aniline ions, alkalis and alkaline earths except Cs are bonded to aniline through water bridges and transition metal cations are coordinated to aniline partly directly and partly through water bridges. Sorption does not occur in the complete absence of water.     

Free fatty acid inhibition of the insulin induction of glucose-6-phosphate dehydrogenase in rat hepatocyte monolayers

Rat hepatocytes in monolayer culture were utilized to determine if the decrease in glucose-6-phosphate dehydrogenase (G6PD) activity resulting from the ingestion of fat can be mimicked by the addition of fatty acids to a chemically, hormonally defined medium. G6PD activity in cultured hepatocytes was induced several-fold by insulin. Dexamethasone or T3 did not amplify the insulin induction of G6PD. Glucose alone increased G6PD activity in cultured hepatocytes from fasted donors by nearly 500%. Insulin in combination with glucose induced G6PD an additional two-fold. The increase in G6PD activity caused by glucose was greater in hepatocytes isolated from 72 hr-fasted rats as compared to fed donor rats. Such a response was reminiscent of the “overshoot” phenomenon in which G6PD activity is induced well above the normal level by fasting-refeeding rats a high glucose diet. Addition of linoleate to the medium resulted in a significant suppression of insulin’s ability to induce G6PD, but linoleate had no effect on the induction of G6PD activity by glucose alone. A shift to the right in the insulin-response curve for the induction of G6PD also was detected for the induction of malic enzyme and acetyl-CoA carboxylase. Arachidonate (0.25 mM) was a significantly more effective inhibitor of the insulin action than linoleate was. Apparently rat hepatocytes in monolayer culture can be utilized as a model to investigate the molecular mechanism by which fatty acids inhibit the production of lipogenic enzymes. In part, this mechanism of fatty acid inhibition involves desensitization of hepatocytes to the lipogenic action of insulin.     

Designing smarter touch-based interfaces for educational contexts

In next-generation classrooms and educational environments, interactive technologies such as surface computing, natural gesture interfaces, and mobile devices will enable new means of motivating and engaging students in active learning. Our foundational studies provide a corpus of over 10,000 touch interactions and nearly 7,000 gestures collected from nearly 70 adults and children aged 7 years and above, which can help us understand the characteristics of children’s interactions in these modalities and how they differ from adults. Based on these data, we identify key design and implementation challenges of supporting children’s touch and gesture interactions, and we suggest ways to address them. For example, we find children have more trouble successfully acquiring onscreen targets and having their gestures recognized than do adults, especially the youngest age group (7–10 years old). The contributions of this work provide a foundation that will enable touch-based interactive educational apps that increase student success.     

The extrusion of polymers below their melting temperatures by the application of high pressures

A number of polymers have been “cold” extruded (i.e. at temperatures well below their normal melting temperatures) by the application of relatively high pressures. In all cases extrudates of relatively large cross-sectional area have been produced, and non-circular cross-sections have also been extruded. The extruded products has been evaluated and the results discussed. In general it has been found that whilst extrusion gives an oriented product, the increase in tensile modulus is much less than for a comparably drawn fibre. This phenomenon has been discussed in terms of the changes in crystalline structure produced by extrusion.     

Kinetic theory of polymer crystal growth applied to melt crystallization of low molecular weight poly(ethylene oxide)

The kinetic theory of polymer crystal growth from the melt is extended to polymers with finite molecular weight and small numbers of folds per molecule. The theory is applied specifically to poly(ethylene oxide), where the most detailed experimental data are available on the growth of crystals from low molecular weight fractions. Predicted curves of growth-rate versus temperature show extensive qualitative agreement with experiment, including increasing chain-folding with increasing molecular weight or supercooling. In the theory this arises from the assumption that molecules have no freedom of lengthwise position within a surface nucleus. It may provide a general rationalization for chain-folding, but could possibly be a consequence of end-group pairing in the special case of OH-terminated poly(ethylene oxide). The theory also explains the sharpness of observed transitions between growth-modes with different numbers of folds per molecule, and the changes in shape of crystals near the transition. Reasonable quantitative agreement with experiment is found in the two cases of high molecular weight and high degrees of supercooling. For low molecular weights and small supercoolings, however, there is a large quantitative discrepancy between the predicted and observed separations of adjacent branches of each growth-rate/temperature curve. This appears to be inexplicable in terms of existing understanding of polymer crystal growth. An Appendix is given which outlines the effects on the theory of relaxing various assumptions of the growth model.     

Supported Alumina Members by an in-Situ Sol–Gel Method

Alumina membranes were prepared using a sol–gel process. Thin gel layers were grown onto porous alumina support tubes by using the permeation of water through the tube to control the rate of hydrolysis. Optimum coating conditions were found to be an ASB to 2-propanol volume ratio of 1:25, coating times between 10 and 15 s, and partial drying times between 2.5 and 3 min, depending on whether the water was flowing in the tube or stored in the tube. The coatings remained crack-free and adherent when fired to 800°C.     

Lipase PS-catalyzed transesterification of citronellyl butyrate and geranyl caproate: Effect of reaction parameters

Pseudomonas sp. lipase PS was immobilized by adsorption and tested for its ability to catalyze the synthesis of citronellyl butyrate and geranyl caproate by transesterification in n-hexane. The reaction parameters investigated were: enzyme load, effect of substrate concentration, added water, temperature, time course, organic solvent, pH memory, and enzyme reuse. Yields as high as 96 and 99% were obtained for citronellyl butyrate and geranyl caproate, respectively, with 300 units (approx. 15% w/w of reactants) of lipase PS. Increasing amounts of terpene alcohol inhibited lipase activity, while excess acyl donor (triacylglycerol) concentration enhanced ester production. Optimal yields were obtained at temperatures from 30–50°C after 24-h incubation time. Yields of 90 and 99% were obtained for citronellyl and geranyl esters, respectively, with 2% added water. Solvents with log P values ≥ 2.5 showed the highest conversion yields. pH 7 and 6–8 seemed to be ideal for citronellyl butyrate and geraniol caproate, respectively. The lipase remained active after reusing 12 times.     

A biomarker of n−3 compliance in patients taking fish oil for rheumatoid arthritis

Dietary fish oil supplements have been shown to have benefits in rheumatoid arthritis (RA), other inflammatory diseases, and in cardiovascular disease. As with any medical advice, variability will exist with regard to adherence and consequent biochemical or pharmacophysiologic effects. The aim was to explore the utility of plasma phospholipid EPA as a measure of n−3 PUFA intake and response to standardized therapeutic advice given in an outpatient or office practice setting, to increase dietary n−3 PUFA, including a fish oil supplement. Patients with early RA were given verbal and written advice to alter their dietary n−3 PUFA intake, including ingestion of 20 mL of bottled fish oil on juice daily. The advice included instructions to increase n−3 PUFA and to avoid foods rich in n−6 PUFA. Every 3 mon, blood samples were obtained for analysis of plasma phospholipid FA. Plasma phospholipid EPA was used as the primary index of n−3 PUFA intake. A diverse response was seen, with about one-third of patients achieving a substantial elevation of plasma phospholipid EPA over the 12-mon study period. A third had little change, with the remainder achieving intermediate levels. Data obtained longitudinally from individual patients indicated that substantial elevations of EPA (>5% total plasma phospholipid FA) could be maintained for more than 3 yr. Plasma phospholipid EPA is a convenient measure of adherence to advice to take a dietary n−3 PUFA-rich fish oil supplement. This measure may prove a useful adjunct to intention to treat analyses in determining the effect of dietary fish oil supplements on long-term outcomes in arthritis and other chronic inflammatory diseases. It may also provide a guide to the effectiveness of therapeutic and preventive messages designed to increase n−3 PUFA intake.