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Carbon potential

Two other components, methanol and benzene, were included in this study. Methanol is important in processes using Rectisol Systems for C02 removal prior to methanation. Benzene was considered in order to determine the effect of aromatics on catalyst activity and potential carbon formation. [Pg.62]

If a potential carbon monoxide hazard is identified, or confirmed by atmospheric monitoring, the range of control techniques summarized on pages 47—51 must be applied. [Pg.63]

The potential carbon-carbon correlations from C14 are shown in grey on the structures that follow the observed correlation is denoted by a solid grey bond while the other correlations are designated by dashed grey bonds. [Pg.259]

The stable isotopic approach can be used to develop carbon budgets for individual sampling points in fields and can be used to develop contour maps (Fig. 8.7). These contour maps visualize the relationships between landscape position and potential carbon storage. In this budget, less new carbon was incorporated into summit shoulder... [Pg.208]

Agarwal AK, Mehendale HM. 1984c. Excessive hepatic accumulation of intracellular calcium in chlordecone potentiated carbon tetrachloride toxicity. Toxicology 30(1) 17-24. [Pg.234]

Bell AN, Young RA, Lockard VG, et al. 1988. Protection of chlordecone-potentiated carbon tetrachloride hepatotoxicity and lethality by partial hepatectomy. Arch Toxicol 61 392-405. [Pg.238]

Kodavanti PR, Joshi UM, Mehendale HM, et al. 1989a. Chlordecone (Kepone )- potentiated carbon tetrachloride hepatotoxicity in partially hepatectomized rats A histomorphometric study. J Appl Toxicol 9(6) 367-375. [Pg.267]

Kodavanti PR S, Kodavanti UP, Mehendale HM. 1990b. Altered hepatic energy status in chlordecone (Kepone)-potentiated carbon tetrachloride hepatotoxicity. Biochem Pharmacol 40(4) 859-866. [Pg.267]

Kodavanti PRA, Rao VC, Mehendale HM. 1993. Loss of calcium homeostasis leads to progressive phase of chlordecone-potentiated carbon tetrachloride hepatotoxicity. Toxicol Appl Pharinaeol 122 77- 87. [Pg.267]

Rao SB, Mehendale HM. 1989. Protection from chlordecone (Kepone)-potentiated carbon tetrachloride hepatotoxicity in rats by fructose 1,6-diphosphate. Int J Biochem 21(9) 949-954. [Pg.280]

Rao SB, Young RA, Mehendale HM. 1989. Hepatic polyamines and related enzymes following chlordecone-potentiated carbon tetrachloride toxicity in rats. J Biochem Toxicol 4(1) 55-63. [Pg.280]

The process of tree growth utilizes atmospheric carbon in the production of wood biomass. Furthermore, this sequestered carbon can continue to be held in products that are manufactured from wood. Although much research has been done in investigating forests as actual or potential carbon sinks, there has been rather less work looking at the implications of the use of wood products as a medium-term carbon store. [Pg.9]

From this perspective, the high-temperature reactions are a potential carbonate buffering system. [Pg.486]

Haloalkanes. Certain haloalkanes and haloalkane-containing mixtures have been demonstrated to potentiate carbon tetrachloride hepatotoxicity. Pretreatment of rats with trichloroethylene (TCE) enhanced carbon tetrachloride-induced hepatotoxicity, and a mixture of nontoxic doses of TCE and carbon tetrachloride elicited moderate to severe liver injury (Pessayre et al. 1982). The researchers believed that the interaction was mediated by TCE itself rather than its metabolites. TCE can also potentiate hepatic damage produced by low (10 ppm) concentrations of carbon tetrachloride in ethanol pretreated rats (Ikatsu and Nakajima 1992). Acetone was a more potent potentiator of carbon tetrachloride hepatotoxicity than was TCE, and acetone pretreatment also enhanced the hepatotoxic response of rats to a TCE-carbon tetrachloride mixture (Charbonneau et al. 1986). The potentiating action of acetone may involve not only increased metabolic activation of TCE and/or carbon tetrachloride, but also possible alteration of the integrity of organelle membranes. Carbon tetrachloride-induced liver necrosis and lipid peroxidation in the rat has been reported to be potentiated by 1,2- dichloroethane in an interaction that does not involve depletion of reduced liver glutathione, and that is prevented by vitamin E (Aragno et al. 1992). [Pg.91]

It is important to note that the relative velocity of an uneventful oxidation of an alcohol with PCC versus a carbon-carbon bond breakage from a chromate ester, driven by the generation of a stable carbocation, is substantially substrate-dependent, and may change according to stereoelec-tronic factors, which may be difficult to predict. Thus, many alcohols are successfully oxidized to aldehydes and ketones, regardless of an apparently potential carbon-carbon bond breakage leading to stabilized carboca-tions.315 Consequently, failure to try an alcohol oxidation with PCC, because of fear of this side reaction is not recommended. [Pg.70]

While the most prevalent, C—H - 0 hydrogen bonds are not the only form of weak hydrogen bond with crystal engineering potential. Carbon acid interactions of type C—H---N, C—H - - Cl and C—H-- - ras well as interactions to weak acceptors such as O—H rand N—H--- n, have all been observed. A report by Roger Hunter of the University of Cape Town, South Africa,97 describes the observation of a sandwich-like pair of C—H-- - n interactions in which two molecules of Ph3PMe+... [Pg.552]

Dutta, K., Schuur, E. A. G., Neff, J. C., and Zimov, S. A. (2006). Potential carbon release from permafrost soils of Northeastern Siberia. Global Change Biol. 12(12), 2336-2351. [Pg.263]

Carbon dioxide Natural and industrial potential carbon sources exist volcanic activity, living organism respiration, fossil fuel combustion, cement production, changes in land use. Natural CO2 fluxes into and out of the atmosphere exceed the human contribution by more than an order of magnitude. The rise in atmospheric CO2 concentration closely parallels the emission history from fossil fuels and land use changes. [Pg.10]

The mercury contamination of significant amounts of mustard agent stockpiled at TOCDF is another factor influencing potential carbon disposition. TOCDF is implementing a pollution abatement system filtration system (PFS) that will trap mercury on carbon. The resulting secondary waste stream consisting of carbon with adsorbed mercury will present a unique disposal problem.14... [Pg.64]

The various support materials have different effects on potential carbon formation. This seems to go in parallel with the Lewis/Bronsted acidity. The main commercially used catalyst supports can be ranked as follows in decreasing order of carbon forming tendency (and thus in decreasing order of the important minimum practical steam/ carbon ratio) a-alumina > magnesium aluminate (spinel) > calcium aluminate > alkalized calcium aluminate [419],... [Pg.76]

Trichloroethylene, tetrachloroethylene, and chloroform potentiate carbon tetrachloride-induced lipid peroxidation in insolated rat hepatocytesJ17,18 ... [Pg.499]

Lignocellulosic biomass refers to plant-derived material such as bagasse, com stover, wheat straw, rice straw, wood chips and switch grass. It is an abundant and renewable resource which is also potentially carbon-neutral and potentially economically viable if appropriate processing methods can be developed to extract and... [Pg.16]


See other pages where Carbon potential is mentioned: [Pg.346]    [Pg.199]    [Pg.236]    [Pg.88]    [Pg.133]    [Pg.116]    [Pg.247]    [Pg.206]    [Pg.509]    [Pg.78]    [Pg.89]    [Pg.90]    [Pg.90]    [Pg.91]    [Pg.279]    [Pg.416]    [Pg.177]    [Pg.105]    [Pg.561]    [Pg.18]    [Pg.243]    [Pg.178]    [Pg.263]    [Pg.8]   
See also in sourсe #XX -- [ Pg.235 ]




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Action potential activated carbonate

Atomic potentials 5-carbon atoms

Calcium carbonate precipitation potential

Carbon adsorption potential

Carbon cylindrical pores, potential energy

Carbon dioxide emissions potential

Carbon dioxide global warming potential

Carbon dioxide reduction current potential

Carbon dioxide reduction electrode potential

Carbon dioxide reduction potential

Carbon electrode potentials

Carbon electrodes potential range

Carbon first ionization potential

Carbon ionization potential

Carbon monoxide ionization potentials

Carbon nanotubes potential

Carbon phase potential

Carbon potential dependence

Carbon potential effect

Carbon potential effect electrochemical oxidation

Carbon reduction potentials

Carbon standard potential

Carbon zeta potential

Carbonate ionization potential

Carbonate reduction potential

Carbonation potential mapping

Coarse-Grained Intermolecular Potentials Derived from the Effective Fragment Potential Application to Water, Benzene, and Carbon Tetrachloride

Electrostatic potential carbon dioxide

Fullerene/carbon nanotube application potential

Graphitized carbon electrostatic potential

Jatropha Oil as a Potential Carbon Source for PHA Production

Other perethynylated compounds as potential monomers for carbon networks

Pairwise potential carbon models

Potential Effects of Dissolved Organic Carbon (DOC) on SPMD Calibration Data

Propylene carbonate decomposition potentials

Towards a General Carbon Potential

Vinylene carbonate oxidation potential

Vinylene carbonate reduction potential

Zeta potential carbon black dispersions

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