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Methanol binding

Fig. 9. Proposed function of electrochemical and Na potentials in energy conservation coupled to methanol disproportionation to CH4 and CO2- It is assumed that prior to oxidation methanol binds first to coenzyme M and that the oxidation is mechanistically and energetically the reversal of CO2 reduction to methyl-coenzyme M. The Na /H" antiporter is involved in the generation of A/iNa Ifom AjlVt. CHO-MFR, formyl-methanofuran CH2=H4MPT, methylene-tetrahydromethanopterin CH3-H4MPT, methyl-tetrahydromethanopterin CH3-S-C0M, methyl-coenzymeM. The hatched boxes indicate membrane-bound electron transport chains or membrane-bound methyltransferase catalyzing either Na or H translocation (see Figs. 5, 6 and 12). ATP is synthesized via membrane-bound H -translocating ATP synthase. The stoichiometries of Na and of translocation were taken from refs. [105,107,167]. x, y and z are unknown stoichiometric factors. Fig. 9. Proposed function of electrochemical and Na potentials in energy conservation coupled to methanol disproportionation to CH4 and CO2- It is assumed that prior to oxidation methanol binds first to coenzyme M and that the oxidation is mechanistically and energetically the reversal of CO2 reduction to methyl-coenzyme M. The Na /H" antiporter is involved in the generation of A/iNa Ifom AjlVt. CHO-MFR, formyl-methanofuran CH2=H4MPT, methylene-tetrahydromethanopterin CH3-H4MPT, methyl-tetrahydromethanopterin CH3-S-C0M, methyl-coenzymeM. The hatched boxes indicate membrane-bound electron transport chains or membrane-bound methyltransferase catalyzing either Na or H translocation (see Figs. 5, 6 and 12). ATP is synthesized via membrane-bound H -translocating ATP synthase. The stoichiometries of Na and of translocation were taken from refs. [105,107,167]. x, y and z are unknown stoichiometric factors.
Inhibition of bovine CA by 5-methyl-l,10-phenanthroline and aniline involves direct tertiary co-ordination to the zinc ion. With the latter reagent, however, H n.m.r. relaxation of metal-bound water is unchanged on aniline co-ordination suggesting either that a histidine ligand is replaced or that a fifth co-ordination site is available. By contrast, methanol binds at a hydrophobic region ca. 6 A from the metal site and shows non-competitive inhibition of p-nitrophenyl acetate hydrolysis activity. ... [Pg.361]

Poly(ethylene oxide) associates in solution with certain electrolytes (48—52). For example, high molecular weight species of poly(ethylene oxide) readily dissolve in methanol that contains 0.5 wt % KI, although the resin does not remain in methanol solution at room temperature. This salting-in effect has been attributed to ion binding, which prevents coagulation in the nonsolvent. Complexes with electrolytes, in particular lithium salts, have received widespread attention on account of the potential for using these materials in a polymeric battery. The performance of soHd electrolytes based on poly(ethylene oxide) in terms of ion transport and conductivity has been discussed (53—58). The use of complexes of poly(ethylene oxide) in analytical chemistry has also been reviewed (59). [Pg.342]

Chaput, Jeminet and Juillard measured the association constants of several simple polyethylene glycols with Na", K", Cs", and Tl". Phase transfer catalytic processes and most biological processes are more likely to involve the first two cations rather than the latter two, so we will confine the discussion to these. Stability constants for the dimethyl ethers of tetra-, penta-, hexa-, and heptaethylene glycols were determined poten-tiometrically in anhydrous methanol solution and are shown in Table 7.1. In the third column of the table, the ratio of binding constants (Ks/K s) is calculated. Note that Simon and his coworkers have referred to this ratio as the selectivity constant. ... [Pg.312]

In the chemical industry, simple aldehydes and ketones are produced in large quantities for use as solvents and as starting materials to prepare a host of other compounds. For example, more than 1.9 million tons per year of formaldehyde, H2C=0, is produced in the United States for use in building insulation materials and in the adhesive resins that bind particle hoard and plywood. Acetone, (CH.3)2C"0, is widely used as an industrial solvent approximately 1.2 million tons per year is produced in the United States. Formaldehyde is synthesized industrial ) by catalytic oxidation of methanol, and one method of acetone preparation involves oxidation of 2-propanol. [Pg.695]

The presence of impurities is an important issue in mobile applications where the hydrogen at least initially will be supplied by the decomposition of hydrocarbons or methanol in on-board reformer systems as long as no appropriate hydrogen storage media are available. In such systems CO is an unavoidable by-product, and since CO binds more strongly to Pt than hydrogen, the low operating temperature... [Pg.343]

Crude chloroform-methanol-water (30 60 8, v/v) extracts of immunostainedTLC bands were analyzed without further purification by nanoelectrospray low-energy mass spectrometry. The authors showed that this effective PLC/MS-joined procedure offers a wide range of applications for any carbohydrate-binding agents such as bacterial toxins, plant lectins, and others. Phenyl-boronic acid (PBA) immobilized on stationary support phases can be put to similar applications. This technology, named boronate affinity chromatography (BAC), consists of a chemical reaction of 1,2- and 1,3-diols with the bonded-phase PBA to form a stable... [Pg.209]

Poisoning of platinum fuel cell catalysts by CO is undoubtedly one of the most severe problems in fuel cell anode catalysis. As shown in Fig. 6.1, CO is a strongly bonded intermediate in methanol (and ethanol) oxidation. It is also a side product in the reformation of hydrocarbons to hydrogen and carbon dioxide, and as such blocks platinum sites for hydrogen oxidation. Not surprisingly, CO electrooxidation is one of the most intensively smdied electrocatalytic reactions, and there is a continued search for CO-tolerant anode materials that are able to either bind CO weakly but still oxidize hydrogen, or that oxidize CO at significantly reduced overpotential. [Pg.161]

Hagemeister, F. C., Gruenloh, C. J., Zwier, T. S., 1998, Density Functional Theory Calculations of the Structures, Binding Energies, and Infrared Spectra of Methanol Clusters , J. Phys. Chem. A, 102, 82. [Pg.289]

The elution of [60]- and [70]fullerenes was measured in water-methanol as a function of temperature on a poly(octadecylsiloxane) phase.67 The retention was shown to be dependent on the surface tension of the stationary phase through a simple geometrical model in which the solute formed a cavity in the stationary phase. In affinity chromatography, it was demonstrated that low ligand density may be a requirement for specificity of binding.68... [Pg.65]


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See also in sourсe #XX -- [ Pg.227 , Pg.390 , Pg.402 ]




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