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Mmol G (mmol + g)
Selected AbstractsAssociation between fatigue and failure to preserve cerebral energy turnover during prolonged exerciseACTA PHYSIOLOGICA, Issue 1 2003L. Nybo Abstract Aim: This study evaluated if the fatigue and apathy arising during exercise with hypoglycaemia could relate to a lowering of the cerebral metabolic rates of glucose and oxygen. Methods and results: Six males completed 3 h of cycling with or without glucose supplementation in random order. Cerebral blood flow, metabolism and interleukin-6 (IL-6) release were evaluated with the Kety,Schmidt technique. Blood glucose was maintained during the glucose trial, while it decreased from 5.2 ± 0.1 to 2.9 ± 0.3 mmol L,1 (mean ± SE) after 180 min of exercise in the placebo trial with a concomitant increase in perceived exertion (P < 0.05). During hypoglycaemia, the cerebral glucose uptake was reduced from 0.34 ± 0.05 to 0.28 ± 0.04 ,mol g,1 min,1, while the cerebral uptake of , -hydroxybutyrate increased to 5 ± 1 pmol g,1 min,1 (P < 0.05). The reduced glucose uptake was accompanied by a lowering of the cerebral metabolic rate of oxygen from 1.84 ± 0.19 mmol g,1 min,1 during exercise with glucose supplementation to 1.60 ± 0.16 mmol g,1 min,1 during hypoglycaemia (P < 0.05). In addition, the cerebral IL-6 release was reduced from 0.4 ± 0.1 to 0.0 ± 0.1 pg g,1 min,1 (P < 0.05). Conclusions: Exercise-induced hypoglycaemia limits the cerebral uptake of glucose, exacerbates exercise, reduces the cerebral metabolic rate of oxygen and attenuates the release of IL-6 from the brain. [source] Zeolite synthesis employing alkaline waste effluents from the aluminum industryENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 2 2002A. La Iglesia Zeolites 4A, 13X, Y, and HZSM5 have been synthesized from alkaline residues from aluminum finishing plants. These residues could contain concentrations of sodium aluminate and sodium hydroxide between 200 and 300 Kg/m3, and small concentrations of heavy metal cations (Cd, Co, Cr, Cu, Mn, and Zn). These contaminants make handling and disposal of these residues difficult. However, the physicochemical properties of the synthesized zeolites (cation exchange capacity of 3 mmol g,1, specific surface area between 600,900 m2g,1, particle size distribution between 0.5,2 ,m and whiteness of 97%) make them useful as detergents and catalysts. Analysis of the chemical composition of the raw materials and the reaction products demonstrates that the heavy metal cation content in the synthesized zeolites is low enough to allow their industrial use (lower than that of the original residues). Therefore, the production of various types of zeolites for industrial use could be used for the elimination of these residues from the aluminum industry. [source] Physiological behaviour of Hanseniaspora guilliermondii in aerobic glucose-limited continuous culturesFEMS YEAST RESEARCH, Issue 2 2003Helena Albergaria Abstract The physiology of Hanseniaspora guilliermondii was studied under aerobic glucose-limited conditions using the accelerostat procedure (continuous acceleration of dilution rate) and classical chemostat cultures. By both cultivation techniques this yeast was found to be Crabtree-positive. Up to a dilution rate of 0.25 h,1, glucose was completely metabolised into biomass, glycerol and carbon dioxide. Above this value, an increase in the dilution rate was accompanied by the production of other metabolites like ethanol, acetic and malic acids. Biomass yield during the purely oxidative growth was 0.49 g g,1 and decreased to 0.26 g g,1 for D=0.34 h,1. A maximal specific ethanol production rate of 1.36 mmol g,1 h,1 and a maximal ethanol yield of 0.05 g g,1 were achieved at D=0.34 h,1. [source] Effect of molecular structure of hybrid precursors on the performances of novel hybrid zwitterionic membranesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Junsheng Liu Abstract Three types of novel hybrid zwitterionic membranes were prepared via a coupling reaction between two silane-coupling agents in a nonaqueous system and a subsequent reaction with 1,4-butyrolactone to create ion pairs in the hybrid precursors. FT-IR spectra corroborated the corresponding reactions. The synthesized membranes were characterized by thermal analyses, ion-exchange capacities, streaming potentials, and pure water flux. Thermal analyses exhibited that the degradation temperature of the hybrid precursors decreased with an increase in zwitterionic extent because of the introduction of ion pairs. Ion-exchange capacity measurements revealed that the anion-exchange capacities and cation-exchange capacities were in the range of 0.023,0.05 and 0.32,0.58 mmol g,1, respectively. Streaming potentials displayed that when the membranes coated for one or three times, the isoelectric points were in the pH range of 6.6,7.58 and 6.58,7.7, respectively. The pure water flux showed that it could be affected by the coating times and the ingredients of these zwitterionic membranes. This difference in membrane's characteristics can be ascribed to the effect of molecular structure of the hybrid precursors. Both the Coulombic interactions of ion pairs between the polymer chains and the hydrophilicity of these membranes were proposed to clarify the above phenomena. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Hydrothermal modification of natural zeolites to improve uptake of ammonium ionsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 4 2005Yujiro Watanabe Abstract The modification of natural zeolites was carried out under hydrothermal conditions to improve the effectiveness of the uptake of ammonium ions. Natural zeolites originating in Japan, such as mordenite and clinoptilolite with quartz, feldspar and a trace of layered silicate, were treated with 0.1, 0.3, 1.0 and 3.0 M NaOH solutions at temperatures from 25 to 150 °C under autogenous pressure for 7 days. After the hydrothermal treatment, the transformation of the zeolites to phillipsite, hydroxyl-sodalite and analcime was observed, depending on the temperature and NaOH concentration. The amounts of ammonium ions taken up into the hydrothermally-treated zeolites were compared with those of the starting materials. The treated products, containing mainly phillipsite, took up twice the amount of ammonium ions as the starting materials. The maximum uptake of ammonium ions was 1.92 mmol g,1. The number of ammonium ions taken up into phillipsite was equal to the number of Na+ ions released from phillipsite. These results indicate that the uptake of ammonium ions proceeds by an ion-exchange mechanism with Na+ ions. Copyright © 2005 Society of Chemical Industry [source] Copper-mediated radical polymerization on a microcellular monolith surfaceJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2004Laurence Moine Abstract High-capacity microcellular monoliths were prepared by a two-step process, including the synthesis of a bromoester-functionalized scaffold by the copolymerization of a highly concentrated emulsion and an in situ surface polymerization of methyl methacrylate with atom transfer radical polymerization. The influence of various parameters, such as the feed ratio, the concentration of immobilized bromoester groups, and the presence of a spacer group on the poly(methyl methacrylate) loading, was studied. Monoliths with capacities of up to 7 mmol g,1 were obtained. Thermogravimetric analyses, scanning electron microscopy experiments, and mercury intrusion porosimetry measurements were used for the characterization of the final materials. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1216,1226, 2004 [source] Synthesis and characterization of poly(butylene succinate)/epoxy group functionalized organoclayPOLYMER INTERNATIONAL, Issue 9 2007Guang-Xin Chen Abstract Poly(butylene succinate) (PBS)/clay nanocomposites were prepared by condensation polymerization of 1,4-butanediol and succinic acid in the presence of an organoclay containing epoxy groups (TFC) and titanium(IV) butoxide as a catalyst. The intercalation and exfoliation of the clay layers in the resulting composite were examined using X-ray scattering and transmission electron microscopy. The role of the epoxy groups of TFC was investigated for the improvement of the morphology of the composites. The silicate layers in the composite were exfoliated to a greater extent as the epoxy content of TFC was increased from 0.245 to 0.359 mmol g,1, while only intercalated morphology was obtained when no epoxy was present. The improved morphologies were attributed to the enhanced interfacial interactions between PBS and TFC through a chemical reaction of the epoxy groups with the end groups of the PBS. The nonisothermal crystallization process of the composites as well as that of neat PBS is well represented by the Avrami equation as modified by Jeziorny [Jeziorny A, Polymer19:1142 (1978)]. The crystallization of the composite took place faster as the epoxy content of the clay increased, due to the more effective nucleation of the well-dispersed TFC layers. Copyright © 2007 Society of Chemical Industry [source] Magnetic Nanoparticle Supported Second Generation Hoveyda,Grubbs Catalyst for Metathesis of Unsaturated Fatty Acid EstersADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 16 2009Zhu Yinghuai Abstract The Hoveyda,Grubbs catalyst has been successfully immobilized on surface-modified magnetic nanoparticles with a loading amount of 0.28,mmol ruthenium/g (magnetic support). The supported catalysts were active for the self-metathesis of methyl oleate and macro-monomer in a quantitative conversion, respectively. In addition, the catalyst can be easily separated by using a magnet and reused several times with sustained activity. [source] | ||||||||||||||||