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Primary Carbon Source (primary + carbon_source)
Selected AbstractsA time-dependent multiphysics, multiphase modeling framework for carbon nanotube synthesis using chemical vapor depositionAICHE JOURNAL, Issue 12 2009Mahmoud Reza Hosseini Abstract A time-dependent multiphysics, multiphase model is proposed and fully developed here to describe carbon nanotubes (CNTs) fabrication using chemical vapor deposition (CVD). The fully integrated model accounts for chemical reaction as well as fluid, heat, and mass transport phenomena. The feed components for the CVD process are methane (CH4), as the primary carbon source, and hydrogen (H2). Numerous simulations are performed for a wide range of fabrication temperatures (973.15,1273.15 K) as well as different CH4 (500,1000 sccm) and H2 (250,750 sccm) flow rates. The effect of temperature, total flow rate, and feed mixture ratio on CNTs growth rate as well as the effect of amorphous carbon formation on the final product are calculated and compared with experimental results. The outcomes from this study provide a fundamental understanding and basis for the design of an efficient CNT fabrication process that is capable of producing a high yield of CNTs, with a minimum amount of amorphous carbon. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Effect of fluorocitrate on cerebral oxidation of lactate and glucose in freely moving ratsJOURNAL OF NEUROCHEMISTRY, Issue 1 2007H. Ronald Zielke Abstract Glucose is the primary carbon source to enter the adult brain for catabolic and anabolic reactions. Some studies suggest that astrocytes may metabolize glucose to lactate; the latter serving as a preferential substrate for neurons, especially during neuronal activation. The current study utilizes the aconitase inhibitor fluorocitrate to differentially inhibit oxidative metabolism in glial cells in vivo. Oxidative metabolism of 14C-lactate and14C-glucose was monitored in vivo using microdialysis and quantitating 14CO2 in the microdialysis eluate following pulse labeling of the interstitial glucose or lactate pool. After establishing a baseline oxidation rate, fluorocitrate was added to the perfusate. Neither lactate nor glucose oxidation was affected by 5 ,mol/L fluorocitrate. However, 20 and 100 ,mol/L fluorocitrate reduced lactate oxidation by 55 ± 20% and 68 ± 12%, respectively (p < 0.05 for both). Twenty and 100 ,mol/L fluorocitrate reduced 14C-glucose oxidation by 50 ± 14% (p < 0.05) and 24 ± 19% (ns), respectively. Addition of non-radioactive lactate to 14C-glucose plus fluorocitrate decreased 14C-glucose oxidation by an additional 29% and 38%, respectively. These results indicate that astrocytes oxidize about 50% of the interstitial lactate and about 35% of the glucose. By subtraction, neurons metabolize a maximum of 50% of the interstitial lactate and 65% of the interstitial glucose. [source] Variation in oxygen isotope fractionation during cellulose synthesis: intramolecular and biosynthetic effectsPLANT CELL & ENVIRONMENT, Issue 10 2006LEONEL STERNBERG ABSTRACT The oxygen isotopic composition of plant cellulose is commonly used for the interpretations of climate, ecophysiology and dendrochronology in both modern and palaeoenvironments. Further applications of this analytical tool depends on our in-depth knowledge of the isotopic fractionations associated with the biochemical pathways leading to cellulose. Here, we test two important assumptions regarding isotopic effects resulting from the location of oxygen in the carbohydrate moiety and the biosynthetic pathway towards cellulose synthesis. We show that the oxygen isotopic fractionation of the oxygen attached to carbon 2 of the glucose moieties differs from the average fractionation of the oxygens attached to carbons 3,6 from cellulose by at least 9%, for cellulose synthesized within seedlings of two different species (Triticum aestivum L. and Ricinus communis L.). The fractionation for a given oxygen in cellulose synthesized by the Triticum seedlings, which have starch as their primary carbon source, is different than the corresponding fractionation in Ricinus seedlings, within which lipids are the primary carbon source. This observation shows that the biosynthetic pathway towards cellulose affects oxygen isotope partitioning, a fact heretofore undemonstrated. Our findings may explain the species-dependent variability in the overall oxygen isotope fractionation during cellulose synthesis, and may provide much-needed insight for palaeoclimate reconstruction using fossil cellulose. [source] Reciprocal 13C-Labeling: A Method for Investigating the Catabolism of CosubstratesBIOTECHNOLOGY PROGRESS, Issue 2 2002Bjarke Christensen The principle of reciprocal labeling is to use a uniformly 13C-labeled substrate as the primary carbon source and a naturally labeled cosubstrate. Metabolites derived from a naturally labeled cosubstrate, in this case amino acids, can then be identified by their relatively lower content of 13C, and information on the degradation pathway can be deduced. The technique is based on GC,MS measurements of amino acid labeling patterns, making the technique well suited for investigating the relative importance of amino acid biosynthesis and amino acid uptake from the medium, as the 13C content of the amino acids incorporated into biomass is a direct measure of the amino acid biosyntheses. The technique is illustrated by the investigation of the degradation of phenoxyacetic acid, a medium component that is essential for production of penicillin V by Penicillium chrysogenum. Glucose was used as the uniformly labeled primary carbon source. [source] | ||||||||||