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CO2 stabilization

The potentials of CO2 reduction is well correlated with the heat of fusion of the electrode metals (Fig. 9). The heat of fusion is related to the extent of d electron contribution to metallic bond °, and may be taken as a measure of d electron a ilability d electron availability will affect the back donation and thus determine the extent of the stabilization of adsorbed CO2 . Stabilized CO2 will have the extra negative charge on O atoms like CO2 coordinating... [Pg.135]

Gold electrodes yield CO in CO2 reduction in aqueous me-Some papers reported kinetic aspects of the reaction. CO formation begins at -0.8 V vs. SHE. Such a low overpotential strongly suggests that the formation of CO takes place with intermediate intervention of CO2 " stabilized by adsorp-... [Pg.141]

Table 1 Percent of injected CO2 permanently sequestered from the atmosphere as a function of atmospheric CO2 stabilization concentration... Table 1 Percent of injected CO2 permanently sequestered from the atmosphere as a function of atmospheric CO2 stabilization concentration...
Kasche, V., R. Schlothauer, and G. Brunner. 1988. Enzyme Denaturation in Supercritical CO2 Stabilizing Effect of S-S Bonds During the Depressurization StepT Biotechnology... [Pg.108]

The triazine derivative is mentioned under carbamates, as it originates from Benomyl (11.5.) and at pH >13 intermediarily hydrolizes to an unstable carbamic acid which after elimination of CO2 stabilizes to l-(2-benzimidazolyl)-3-n-butylurea (Chiba Singh, 1986) structural formula ... [Pg.625]

Pro.6Sro 4Coo.5Feo.503 6 CO2 stability and microstructure. Appl. Mater. Interfaces, 6, 10274-10282. [Pg.736]

By far the most common lead salt used for PVC stabilization is tribasic lead sulfate. It can be found either alone or combined with another lead salt in almost every lead-stabilized PVC formulation. Many of the combinations are actually coprecipitated hybrid products, ie, basic lead sulfophthalates. Dibasic lead stearate and lead stearate are generally used as costabilizers combined with other primary lead salts, particularly in rigid PVC formulations where they contribute lubrication properties dibasic lead stearate provides internal lubrication and lead stearate is a good external lubricant. Basic lead carbonate is slowly being replaced by tribasic lead sulfate in most appHcations due the relatively low heat stabiHty of the carbonate salt which releases CO2 at about 180°C during PVC processing. [Pg.551]

Succinic anhydride is stabilized against the deteriorative effects of heat by the addition of small amounts (0.5 wt %) of boric acid (27), the presence of which also decreases the formation of the dilactone of gamma ketopimelic acid (28). Compared with argon, CO2 has an inhibiting effect on the thermal decomposition of succinic acid, whereas air has an accelerating effect (29,30). [Pg.535]

Sludge Stabilization. Organic sludges need to be stabilized before ultimate disposal except in the case of incineration. This is usually achieved by either aerobic or anaerobic digestion. In aerobic digestion, the degradable volatile soHds are Hquefted and oxidized to CO2 and H2O. In anaerobic digestion the soHds are Hquefted and fermented to CH and CO2. [Pg.194]

The rate of dimerization of nitrile A-oxides is strongly influenced by the nature of R. When R = Cl, Br, CO2 alkyl or COR, the nitrile A-oxide cannot be isolated nor obtained in solution for any appreciable time. Table 11 gives the approximate time required for complete dimerization of some nitrile A-oxides (335) to furoxans (336) in benzene solution at 18 °C (70E1169). Evidently, steric and electronic effects dramatically increase the stability... [Pg.66]

Fragmentation reactions are particularly common in small rings. Relief of strain and the gain in stability in forming certain common fragments (such as N2, CO2), as felt in the... [Pg.19]

The catalyst should be the copper-based United Catalyst T-2370 in 3/16 , reduced and stabilized, in extrudate form. Initially, 26.5 g of this should be charged to the catalyst basket. This catalyst is not for methanol synthesis but for the low temperature shift reaction of converting CO to CO2 with steam. At the given conditions it will make methanol at commercial production rates. Somewhat smaller quantity of catalyst can also be used with proportionally cut feed rates to save feed gas. [Pg.83]

The influence of Zn-deposition on Cu(lll) surfaces on methanol synthesis by hydrogenation of CO2 shows that Zn creates sites stabilizing the formate intermediate and thus promotes the hydrogenation process [2.44]. Further publications deal with methane oxidation by various layered rock-salt-type oxides [2.45], poisoning of vana-dia in VOx/Ti02 by K2O, leading to lower reduction capability of the vanadia, because of the formation of [2.46], and interaction of SO2 with Cu, CU2O, and CuO to show the temperature-dependence of SO2 absorption or sulfide formation [2.47]. [Pg.24]

Carbon forms 2 extremely stable oxides, CO and CO2, 3 oxides of considerably lower stability, C3O2, C5O2 and C]209, and a number of unstable or poorly characterized oxides including C2O, C2O3 and the nonstoichiometric graphite oxide (p. 289). Of these, CO and CO2 are of outstanding importance and their chemistry will be discussed in subsequent paragraphs after a few brief remarks about some of the others. [Pg.305]

The solubilities of the various gases in [BMIM][PFg] suggests that this IL should be an excellent candidate for a wide variety of industrially important gas separations. There is also the possibility of performing higher-temperature gas separations, thanks to the high thermal stability of the ILs. For supported liquid membranes this would require the use of ceramic or metallic membranes rather than polymeric ones. Both water vapor and CO2 should be removed easily from natural gas since the ratios of Henry s law constants at 25 °C are -9950 and 32, respectively. It should be possible to scrub CO2 from stack gases composed of N2 and O2. Since we know of no measurements of H2S, SO, or NO solubility in [BMIM][PFg], we do not loiow if it would be possible to remove these contaminants as well. Nonetheless, there appears to be ample opportunity for use of ILs for gas separations on the basis of the widely varying gas solubilities measured thus far. [Pg.91]


See other pages where CO2 stabilization is mentioned: [Pg.117]    [Pg.185]    [Pg.168]    [Pg.136]    [Pg.163]    [Pg.171]    [Pg.357]    [Pg.220]    [Pg.463]    [Pg.15]    [Pg.117]    [Pg.185]    [Pg.168]    [Pg.136]    [Pg.163]    [Pg.171]    [Pg.357]    [Pg.220]    [Pg.463]    [Pg.15]    [Pg.116]    [Pg.16]    [Pg.431]    [Pg.202]    [Pg.386]    [Pg.58]    [Pg.412]    [Pg.145]    [Pg.399]    [Pg.51]    [Pg.334]    [Pg.410]    [Pg.457]    [Pg.64]    [Pg.103]    [Pg.131]    [Pg.53]    [Pg.119]    [Pg.120]    [Pg.210]    [Pg.229]    [Pg.303]    [Pg.687]    [Pg.408]    [Pg.806]    [Pg.1118]   
See also in sourсe #XX -- [ Pg.38 ]




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The CO2-N2 Dimer etc., Stability

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