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Carbon dioxide function

The known carbon dioxide coordination complexes seem to fall into three categories. In the first, carbon dioxide functions as a discrete ligand the only interaction binding the C02 is with the metal itself. There is evidence for two such forms of unsupported coordination through the carbon-oxygen double bond, (21), and through the carbon atom alone, (22). [Pg.122]

Sattler, W. and Parkin, G. (2012) Zinc catalysts for on-demand hydrogen generation and carbon dioxide functionalization./. Am, Chem, Soc., 134, 17462-17465. [Pg.765]

Figure C3.3.11. The energy transfer probability distribution function P(E, E ) (see figure C3.3.2) for two molecules, pyrazine and hexafluorobenzene, excited at 248 nm, arising from collisions with carbon dioxide... Figure C3.3.11. The energy transfer probability distribution function P(E, E ) (see figure C3.3.2) for two molecules, pyrazine and hexafluorobenzene, excited at 248 nm, arising from collisions with carbon dioxide...
Figure C3.3.12. The energy-transfer-probability-distribution function P(E, E ) (see figure C3.3.2 and figure C3.3.11) for two molecules, pyrazine and hexafluorobenzene, excited at 248 nm, arising from collisions with carbon dioxide molecules. Both collisions that leave the carbon dioxide bath molecule in its ground vibrationless state, OO O, and those that excite the 00 1 vibrational state (2349 cm ), have been included in computing this probability. The spikes in the distribution arise from excitation of the carbon dioxide bath 00 1 vibrational mode. Figure C3.3.12. The energy-transfer-probability-distribution function P(E, E ) (see figure C3.3.2 and figure C3.3.11) for two molecules, pyrazine and hexafluorobenzene, excited at 248 nm, arising from collisions with carbon dioxide molecules. Both collisions that leave the carbon dioxide bath molecule in its ground vibrationless state, OO O, and those that excite the 00 1 vibrational state (2349 cm ), have been included in computing this probability. The spikes in the distribution arise from excitation of the carbon dioxide bath 00 1 vibrational mode.
This is an acid-base reaction, in which the base is the oxide ion (p. 89) the acidic oxide SiOj displaces the weaker acidic oxide CO2 in the fused mixture. But in aqueous solution, where the 0 ion cannot function as a strong basefp. 89),carbon dioxide displaces silica, which, therefore, precipitates when the gas is passed through the aqueous silicate solution. In a fused mixture of silica and a nitrate or phosphate, the silica again displaces the weaker acidic oxides N2O5 and P4OJ0 ... [Pg.187]

The carbon-carbon bond forming potential inherent m the Claisen and Dieckmann reac tions has been extensively exploited m organic synthesis Subsequent transformations of the p keto ester products permit the synthesis of other functional groups One of these transformations converts p keto esters to ketones it is based on the fact that p keto acids (not esters ) undergo decarboxylation readily (Section 19 17) Indeed p keto acids and their corresponding carboxylate anions as well lose carbon dioxide so easily that they tend to decarboxylate under the conditions of their formation... [Pg.893]

In keeping with its biogenetic origin m three molecules of acetic acid mevalonic acid has six carbon atoms The conversion of mevalonate to isopentenyl pyrophosphate involves loss of the extra carbon as carbon dioxide First the alcohol hydroxyl groups of mevalonate are converted to phosphate ester functions—they are enzymatically phosphorylated with introduction of a simple phosphate at the tertiary site and a pyrophosphate at the primary site Decarboxylation m concert with loss of the terti ary phosphate introduces a carbon-carbon double bond and gives isopentenyl pyrophos phate the fundamental building block for formation of isoprenoid natural products... [Pg.1091]

Each component of blood has a function ia the body. Red cells transport oxygen and carbon dioxide between the lungs and cells ia the tissues. White cells function as defense of the body. Platelets are important for hemostasis, ie, the maintenance of vascular iategrity. Plasma, an aqueous solution containing various proteias and fatty acids, transports cells, food, and hormones throughout the body. Some proteias ia plasma play a role ia clotting, others are messengers between cells. [Pg.520]

Aldehydes react with alkenylborates to give 1,3-diols upon oxidation of the intermediate (300). Alkynylborates ate transformed by epoxides into homoallyhc alcohols and alkenylborates into 1,4-diols (300,301). Carbon dioxide reacts with alkenylborates to yield catboxyhc acids (302). The scope of these transformations is further extended by the use of functionalized electrophiles and borates, often reacting with high stereoselectivity. For example, in the... [Pg.316]

The performance of SCWO for waste treatment has been demonstrated (15,16). In these studies, a broad number of refractory materials such as chlorinated solvents, polychlorinated biphenyls (PCBs), and pesticides were studied as a function of process parameters (17). The success of these early studies led to pilot studies which showed that chlorinated hydrocarbons, including 1,1,1-trichloroethane /7/-T5-6y,(9-chlorotoluene [95-49-8] and hexachlorocyclohexane, could be destroyed to greater than 99.99997, 99.998, and 99.9993%, respectively. In addition, no traces of organic material could be detected in the gaseous phase, which consisted of carbon dioxide and unreacted oxygen. The pilot unit had a capacity of 3 L/min of Hquid effluent and was operated for a maximum of 24 h. [Pg.499]

In the chloride shift, Ck plays an important role in the transport of carbon dioxide (qv). In the plasma, CO2 is present as HCO, produced in the erythrocytes from CO2. The diffusion of HCO requires the counterdiffusion of another anion to maintain electrical neutraUty. This function is performed by Ck which readily diffuses into and out of the erythrocytes (see Fig. 5). The carbonic anhydrase-mediated Ck—HCO exchange is also important for cellular de novo fatty acid synthesis and myelination in the brain (62). [Pg.381]

Fig. 7. Glass-tiansition tempeiatuies of (A) polymetfiylinetfiaciylate (PMMA) ( ) polymetfiylinetfiaciylate-fo-styiene (SMMA60) and ( ) polystyrene (PS) as a function of carbon dioxide pressure, where the solid line represents CO2 vapor pressure (37). To convert MPa to psi, multiply by 145. Fig. 7. Glass-tiansition tempeiatuies of (A) polymetfiylinetfiaciylate (PMMA) ( ) polymetfiylinetfiaciylate-fo-styiene (SMMA60) and ( ) polystyrene (PS) as a function of carbon dioxide pressure, where the solid line represents CO2 vapor pressure (37). To convert MPa to psi, multiply by 145.
Equations for viscosity at different temperatures, pressures, and thermal conductivity have also been provided (5). The vapor pressure function for carbon dioxide in terms of reduced temperatures and pressure is as foUows ... [Pg.18]

The carbon monoxide concentration of gas streams is a function of many parameters. In general, increased carbon monoxide concentration is found with an increase in the carbon-to-hydrogen ratio in the feed hydrocarbon a decrease in the steam-to-feed-carbon ratio increase in the synthesis gas exit temperature and avoidance of reequiUbration of the gas stream at a temperature lower than the synthesis temperature. Specific improvement in carbon monoxide production by steam reformers is made by recycling by-product carbon dioxide to the process feed inlet of the reformer (83,84). This increases the relative carbon-to-hydrogen ratio of the feed and raises the equiUbrium carbon monoxide concentration of the effluent. [Pg.54]

Flame Temperature. The adiabatic flame temperature, or theoretical flame temperature, is the maximum temperature attained by the products when the reaction goes to completion and the heat fiberated during the reaction is used to raise the temperature of the products. Flame temperatures, as a function of the equivalence ratio, are usually calculated from thermodynamic data when a fuel is burned adiabaticaHy with air. To calculate the adiabatic flame temperature (AFT) without dissociation, for lean to stoichiometric mixtures, complete combustion is assumed. This implies that the products of combustion contain only carbon dioxide, water, nitrogen, oxygen, and sulfur dioxide. [Pg.517]

Sepa.ra.tlon, Sodium carbonate (soda ash) is recovered from a brine by first contacting the brine with carbon dioxide to form sodium bicarbonate. Sodium bicarbonate has a lower solubiUty than sodium carbonate, and it can be readily crystallized. The primary function of crystallization in this process is separation a high percentage of sodium bicarbonate is soHdified in a form that makes subsequent separation of the crystals from the mother hquor economical. With the available pressure drop across filters that separate Hquid and soHd, the capacity of the process is determined by the rate at which hquor flows through the filter cake. That rate is set by the crystal size distribution produced in the crystallizer. [Pg.338]


See other pages where Carbon dioxide function is mentioned: [Pg.1350]    [Pg.240]    [Pg.153]    [Pg.652]    [Pg.1350]    [Pg.240]    [Pg.153]    [Pg.652]    [Pg.81]    [Pg.75]    [Pg.24]    [Pg.485]    [Pg.441]    [Pg.21]    [Pg.28]    [Pg.74]    [Pg.178]    [Pg.249]    [Pg.199]    [Pg.408]    [Pg.434]    [Pg.341]    [Pg.344]    [Pg.27]    [Pg.469]    [Pg.532]    [Pg.150]    [Pg.110]    [Pg.229]    [Pg.223]    [Pg.82]    [Pg.164]    [Pg.2002]    [Pg.2215]    [Pg.2228]    [Pg.2413]    [Pg.34]    [Pg.37]    [Pg.784]   
See also in sourсe #XX -- [ Pg.319 ]




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