Green Catalysis with Alternative Feedstocks

The use of renewable feedstocks, derived from biomass, for the chemical industry is discussed. The modern chemical industry is based around platform chemicals, e.g. ethene, propene, benzene and xylenes, which are readily derived from oil, and using these intermediates a broad range of finished products can be derived. While it is feasible that biomass can be converted to syngas and hence to existing key platform chemicals, this loses all of the chemical complexity that is inherent in bio-derived molecules. In this paper some of the options are considered and, in particular, the oxidation of glucose and glycerol using gold nanoparticles supported on carbon is described. We also contrast the oxidation of glycerol using supported gold and gold–palladium alloys prepared using an impregnation technique, since the gold–palladium alloys have been shown to be highly effective for the oxidation of alcohols and the synthesis of hydrogen peroxide.     

Structural studies of enzyme-based microfluidic biofuel cells

An enzyme-based glucose/O₂ biofuel cell was constructed within a microfluidic channel to study the influence of electrode configuration and fluidic channel height on cell performance. The cell was composed of a bilirubin oxidase (BOD)-adsorbed O₂ cathode and a glucose anode prepared by co-immobilization of glucose dehydrogenase (GDH), diaphorase (Dp) and VK₃-pendant poly-l-lysine. The consumption of O₂ at the upstream cathode protected the downstream anode from interfering O₂ molecules, and consequently improved the cell performance (maximum cell current) ca. 10% for the present cell. The cell performance was also affected by the channel height. The output current and power of a 0.1 mm-height cell was significantly less than those of a 1 mm-height cell because of the depletion of O₂, as determined by the shape of the E–I curve at the cathode. On the other hand, the volume density of current and power was several times higher for the narrower cell.     

Conductometric biosensor based on glucose oxidase and beta-galactosidase for specific lactose determination in milk

This paper investigates the development of a biosensor associating two distinct enzymatic activities, that of the beta-galactosidase and that of the glucose oxidase, in order to apply it for the quantitative detection of lactose in milk. To eliminate interferences with glucose, a differential mode of measurement was used. Results show a linear calibration curve for lactose concentration between 60 and 800 μM (0.03 to 0.3 g/L). Tests with real commercial milk samples were carried out to validate the conductometric biosensor.     

What's wrong with believing in repression?: A review for legal professionals.

Some courts in recent years have tarnished their credibility by willingly and blindly adopting the theory of repressed memory. Such acceptance can destroy the reputations of falsely accused individuals, and, by failing to pay due attention to scientific evidence, gives credence to pseudoscience and demeans the scientific method. This paper was written to inform judges and attorneys about the relevant evidence, which shows that: (a) the concepts of repressed and recovered memory are not generally accepted in the psychological and psychiatric community; (b) the studies cited to support these concepts reveal significant flaws; (c) much empirical evidence has been accumulated against the theory of repression; (d) the studies using the best methodology offer the least support for the repression hypothesis; and (e) there is no evidence that recovered memories accurately reveal the specifics of long-ago events. Repressed- and recovered-memory theory is not supported by science. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Graphene-gold nanostructure composites fabricated by electrodeposition and their electrocatalytic activity toward the oxygen reduction and glucose oxidation

A gold nanoparticles (Au NPs)-graphene nanocomposite (Au-graphene nanocomposite) was prepared by electrochemically depositing Au NPs on the surface of graphene sheets, and characterized by scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), X-ray powder diffraction (XRD), and electrochemical methods. The morphology and size of the Au NPs could be easily controlled by adjusting the electrodeposition time and the concentration of precursor (AuCl₄⁻). The electrocatalytic activities of the nanocomposites toward oxygen reduction and glucose oxidation were investigated by cyclic voltammetry. The results indicated that the nanocomposites had a higher catalytic activity than the Au NPs or graphene alone, indicating the synergistic effect of graphene and Au NPs. Therefore, this study has provided a general route for fabrication of graphene-based noble metal nanomaterials composite, which could be potential utility to fuel cells and bioelectroanalytical chemistry.     

A study on direct glucose and fructose alkaline fuel cell

Direct glucose fuel cell (DGFC) has huge potential as a power source in low power long term portable devices. Electro-oxidation of glucose and fructose on PtRu/C catalyst are studied using cyclic voltammetry in alkaline medium to study the reason for deactivation of glucose fuel cell. A simple direct glucose fuel cell with PtRu/C as anode and activated charcoal as cathode was constructed and operated to study the effect of different temperature and concentration of glucose and KOH. An open-circuit voltage (OCV) of 0.91 V is obtained using 0.3 M glucose in 1 M KOH solution. OCV increased with the increase in glucose concentration. The maximum peak power density of 1.38 mW cm⁻² is obtained using 0.2 M glucose in 1 M KOH at 30 °C and it decreases with further increase in glucose concentration and temperature. In order to determine the reason for decrease in performance of glucose fuel cell due to conversion of glucose to fructose, the fuel cell was operated using 0.2 M fructose in 1 M KOH. The peak power density delivered is 0.57 mW cm⁻². The DGFC is continuously operated for 260 h at constant load of 500 Ω produces final constant voltage of 0.21 V.     

Non‐Conventional Electrochemical Techniques for Assembly of Electrodes on Glassy Carbon‐Like PPF Materials and Their Use in a Glucose Microfluidic Fuel‐Cell

This paper addresses the electrochemical growth of PtAg and Au nanoparticles on pyrolyzed photoresist films (PPFs). The PtAg/PPF electrode was evaluated toward oxygen reduction reaction (ORR) in the absence and presence of glucose; meanwhile the electrocatalytic activity of Au/PPF was investigated for the glucose electrooxidation reaction (GOR) in 0.3 M KOH in the absence and presence of air as an oxygen source. The results obtained using the electrochemical studies showed that the PtAg/PPF electrode exhibited tolerance toward the ORR in the presence of low glucose concentrations. Moreover, Au/PPF showed good affinity toward glucose oxidation at high concentrations (50 and 100 mM) in the presence of oxygen instead further oxidations of glucose by‐products. Both electrocatalysts were evaluated as the cathode (PtAg/PPF) and the anode (Au/PPF) in a glucose microfluidic fuel cell (G‐μFC) constructed using a UV‐lithography technique and several sheets of different polymeric materials. The G‐μFC was tested using 100 mM glucose with 0.3 M KOH as electrolyte in the absence of an external source of nitrogen or oxygen as the fuel at zero flow rate; this cell reached a maximum power density of 0.085 mW cm⁻² using a low Pt loading (approximately 20% of weight percentage) mixed with non‐noble materials, such as Ag.     

Co-consumption of sugars or ethanol and glucose in a Saccharomyces cerevisiae strain deleted in the HXK2 gene

In previous studies it was shown that deletion of the HXK2 gene in Saccharomyces cerevisiae yields a strain that hardly produces ethanol and grows almost exclusively oxidatively in the presence of abundant glucose. This paper reports on physiological studies on the hxk2 deletion strain on mixtures of glucose/sucrose, glucose/galactose, glucose/maltose and glucose/ethanol in aerobic batch cultures. The hxk2 deletion strain co-consumed galactose and sucrose, together with glucose. In addition, co-consumption of glucose and ethanol was observed during the early exponential growth phase. In S.cerevisiae, co-consumption of ethanol and glucose (in the presence of abundant glucose) has never been reported before. The specific respiration rate of the hxk2 deletion strain growing on the glucose/ethanol mixture was 900 micromol.min(-1).(g protein)(-1), which is four to five times higher than that of the hxk2 deletion strain growing oxidatively on glucose, three times higher than its parent growing on ethanol (when respiration is fully derepressed) and is almost 10 times higher than its parent growing on glucose (when respiration is repressed). This indicates that the hxk2 deletion strain has a strongly enhanced oxidative capacity when grown on a mixture of glucose and ethanol.     

Fate of the glucose degradation products 3-deoxyglucosone and glyoxal during peritoneal dialysis

Conventional fluids for peritoneal dialysis (PD) contain reactive glucose degradation products (GDPs) as a result of glucose breakdown during heat-sterilization. GDPs in PD fluids (PDFs) have been associated with the progressive alteration of the peritoneal membrane during long-term PD by cytotoxic effects and formation of advanced glycation endproducts (AGEs). In this study, we investigated the possible fate of two characteristic GDPs, 3-deoxyglucosone (3-DG) and glyoxal, during PD. In vivo, 3-DG and glyoxal concentrations, which were analyzed by high-performance liquid chromatography (HPLC), decreased in PDFs by 78% and 88% during 4 h of dwell time. The PDFs were then incubated in vitro in the presence of the most important reaction partners of GDPs in the peritoneal cavity. Neither human peritoneal mesothelial cells, human peritoneal fibroblasts, soluble protein, an insoluble collagen surface, nor components of spent dialysate led to a significant reduction of 3-DG or glyoxal after 6 h. Only after long-term incubation, a noticeable decrease of 3-DG was observed (-37% after three weeks), more likely due to spontaneous degradation reaction than formation of advanced glycation endproducts. These results suggest that in the course of PD, 3-DG, and glyoxal are absorbed into the organism and thus might contribute to the systemic pool of reactive carbonyl compounds.     

葡萄糖氧化酶及其应用

葡萄糖氧化酶是需氧脱氢酶,易溶于水,不溶于有机溶剂。工业生产多从黑曲霉中提取,该酶主要与过氧化氢酶共同作用催化葡萄糖产生葡萄糖酸,同时消耗氧。葡萄糖氧化酶广泛应用于食品、医药、饲料等行业中,起到了去除葡萄糖、脱氧、杀菌等作用。