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Chemical splitting

Mohapatra SK, Misra M, Mahajan VK et al (2007) A novel method for the synthesis of titania nanotubes using sonoelectrochemical method and its application for photoelectro-chemical splitting of water. J Catal 246 362-369... [Pg.125]

A chemical bias is achieved by using two different electrolytes placed in two half-cells, with the electrolytes being chosen to reduce the voltage required to cause the chemical splitting. An n-Ti02 photoanode 4M KOH 4M HCl Pt-cathode is one example of a chemically biased photoelectrochemical cell [44]. [Pg.124]

The chemistry of electrochemical reaction mechanisms is the most hampered and therefore most in need of catalytic acceleration. Therefore, we understand that electrochemical catalysis does not, in principle, differ much fundamentally and mechanistically from chemical catalysis. In addition, apart from the fact that charge-transfer rates and electrosorption equilibria do depend exponentially on electrode potential—a fact that has no comparable counterpart in chemical heterogeneous catalysis—in many cases electrocatalysis and catalysis of electrochemical and chemical oxidation or reduction processes follow very similar if not the same pathways. For instance as electrochemical hydrogen oxidation and generation is coupled to the chemical splitting of the H2 molecule or its formation from adsorbed hydrogen atoms, respectively, electrocatalysts for cathodic hydrogen evolution—... [Pg.91]

From the sea anemone M. senile was isolated j3-glucopyranosyl-( 1 - l)-ceramide, the structure of which was determined by mass spectrometry, H-n.m.r. spectroscopy, and chemical splitting. The major sphingosine in the cerebroside is a new base containing two double bonds and branching at one double bond, namely, 2-amino-D-eryf/jro-l,3-dihydroxy-9-methyl-( , E)-octadeca-4,8-diene. The major fatty acids are Ci6 0 and C20 o a-hydroxy acids.133... [Pg.411]

From the shell of A. crassipina has been isolated a sulfoquinovosylmono-glyceride, and its structure has been established by chemical splitting (alkaline methanolysis and acid hydrolysis), as well as by such physicochemical methods as H- and l3C-n.m.r. spectroscopy, g.l.c.-mass spectrometry, and field-desorption mass spectrometry.214 The major component was shown to be l-0-hexadecanoyl-3-0-(6-C-sulfo-a-D-quinovosyl)glycerol (96% of the mixture), and the minor one was its analog containing tetradecanoic acid. [Pg.428]

A plot of the efficiency of conversion of solar light to clean hydrogen fuel from water is shown in Fig. 10.27. A maximum efficiency of 8.4% was obtained, and this could be increased to 9.3% by increasing the temperature to 43°C. In 1998 Turner et al. improved upon this and obtained 16% efficiency in the catalyzed photoelectro-chemical splitting of water. [Pg.62]

ALB Manufacturing industrial chemicals—split off from Ethyl... [Pg.493]

Table 5.9. Comparison between the experimental values and spacings (meV) of the Is manifold energy levels showing the amplitude of the valley-orbit/chemical splittings of the group-V donors in silicon and germanium and the calculated values of [2], where no chemical effect is included. More accurate experimental values of the E (Is (Ai)) are given in Tables 6.3 and 6.7... Table 5.9. Comparison between the experimental values and spacings (meV) of the Is manifold energy levels showing the amplitude of the valley-orbit/chemical splittings of the group-V donors in silicon and germanium and the calculated values of [2], where no chemical effect is included. More accurate experimental values of the E (Is (Ai)) are given in Tables 6.3 and 6.7...
The chemical splitting of ester bonds by hydrolysis, alcoholysis or aminolysis are specific reactions of all organic esters, including urethanes (or carbamates) which are in fact esters of carbamic acid. [Pg.516]

High temperature ceramic heat exchangers (HX) either in tube-in-tube or plate type design are promising candidates for the use in harsh corrosive and combustion environments. In contrast to tubes, plate-lype HX with integrated flow channels can contribute to an increasing efficiency of the heat transfer. Those HX can be used for heat recovery processes, thermo chemical splitting reactions or within externally fired combined cycles. [Pg.117]

Sartoretti CJ, Ulmaim M, Alexander BD et al (2003) Photoelectrochemical oxidation of water at transparent ferric oxide film electrodes. Chem Phys Lett 376 194—200 Sartoretti CJ, Alexander BD, Solarska R et al (2005) Photoelectrochemical oxidation of water at transparent ferric oxide film electrodes. J Phys Chem B 109 13685-13692 Kumari S, Singh AP, Sonal et al (2010) Spray pyrolytically deposited nanoporous Ti " doped hematite thin films for efficient photoelectron chemical splitting of water. Int J Hydrogen Energy 35 3985-3990... [Pg.36]

Break foam with hot pipes Water shots in hot oil Rapid depressurization Gamma-ray foam detectors Defoaming chemicals Split liquid levels... [Pg.202]

Determination of the content of oxyethylene groups in ethylene oxide-propylene oxide can also easily be carried out by NMR spectrometry without chemical splitting of the ether linkage, identifying the base compounds by this method is difficult. Several methods for the cleavage of ethers have been studied, but few applied to the identification of the base compounds of the polyurethane polyethers. [Pg.84]

In the last 10 years the increased use of chemical splitting of oils and fats has widened the range of feedstocks for soap making to include non-natural chain-length blends. This provides soap makers with additional opportunities to cost optimize their blends. A farther consequence of this is that soaps made from distilled fatty acids tend to contain lower levels of impurities which in natural oils and fats can have deleterious affects on color and odor. This offers the potential for further cost savings by reduction in levels of minor ingredients such as whiteners and antioxidants. [Pg.60]

One observes the chemical splitting of the Cls line in CH2CH0OH due to the different carbons. In Fig.15 also the valence spectrum or ethanol is recorded. Fig.16 shows that I3 ions are formed in the solution when Nal and I2 are dissolved in ethanol. Each of the I spin 3d components is split in two chemically shifted lines in the intensity ratio of 2 1, provided that the shake-up line is attributed to the externally situated two iodine atoms in the (linear) I ion. [Pg.257]

With the first of these, chemical splitting, final treatment is then in a separator. With the second, thermal splitting, complete process equipment is normally involved, incorporating heat exchangers associated with evaporators or centrifuges. [Pg.316]

The homopolar splitting component, V2, of a heteropolar bond increases exactly as for a homopolar semiconductor according to Equation 5.3 as the interatomic spacing decreases. The chemical splitting also increases with decreasing bond distance d, approximately (see Ferry for discussion) as ... [Pg.204]

If the antibonding states are empty and the bonding states are filled, the localization of the states results in a difference in the charge density around the cation and anion. In other words, as the bands become increasingly connected to given atoms, the bonding becomes more ionic. A quantitative relationship between chemical splitting and ionic character, a, of the bonds can be derived (see, for example Harrison) to be ... [Pg.205]

Molecule Interatomic Distance (A) Homopolar Splitting 2V, CeV) Chemical Splitting, 2C (eV) Bond Energy, 2A(eV) Minimum 300 K Energy Gap (eV)... [Pg.206]

Figure 5.8 Changes in the energy gap of heteropolar semiconduetors made up from elements in row 4 of the periodic table showing the effect of chemical splitting on the energy gap. Values used in generating this figure are from Table 5.2. Figure 5.8 Changes in the energy gap of heteropolar semiconduetors made up from elements in row 4 of the periodic table showing the effect of chemical splitting on the energy gap. Values used in generating this figure are from Table 5.2.
The decreasing variation in energy with momentum across the diagram is not, perhaps, very surprising given the discussion in Section 5.1. As the chemical splitting increases, the bonds become increasingly ionic. Ionic bonds are relatively... [Pg.220]


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See also in sourсe #XX -- [ Pg.124 , Pg.125 , Pg.126 , Pg.127 ]

See also in sourсe #XX -- [ Pg.216 , Pg.217 , Pg.220 , Pg.221 , Pg.224 , Pg.258 , Pg.259 , Pg.297 , Pg.299 , Pg.300 , Pg.318 ]




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