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Combined oxide

Olefins add anhydrous acetic acid to give esters, usually of secondary or tertiary alcohols propjiene [115-07-1] yields isopropyl acetate [108-21-4], isobutjiene [115-11-7] gives tert-huty acetate [540-88-5]. Minute amounts of water inhibit the reaction. Unsaturated esters can be prepared by a combined oxidative esterification over a platinum group metal catalyst. Eor example, ethylene-air-acetic acid passed over a palladium—Hthium acetate catalyst yields vinyl acetate. [Pg.66]

These catalysts contained promoters to minimise SO2 oxidation. Second-generation systems are based on a combined oxidation catalyst and particulate trap to remove HC and CO, and to alleviate particulate emissions on a continuous basis. The next phase will be the development of advanced catalysts for NO removal under oxidising conditions. Low or 2ero sulfur diesel fuel will be an advantage in overall system development. [Pg.173]

An interesting one-step combined oxidation and benzilic acid rearrangement has been described by Holden and Kerwin in connection with the synthesis of C-norpregnanes from 3a,20yS-dihydroxy-5j9-pregnan-12-one (partial structure 85). [Pg.436]

Acetone (2-propanone), is produced from isopropanol by a dehydrogenation, oxidation, or a combined oxidation dehydrogenation route. [Pg.229]

The scope of reactions involving hydrogen peroxide and PTC is large, and some idea of the versatility can be found from Table 4.2. A relatively new combined oxidation/phase transfer catalyst for alkene epoxidation is based on MeRe03 in conjunction with 4-substituted pyridines (e.g. 4-methoxy pyridine), the resulting complex accomplishing both catalytic roles. [Pg.123]

Potential benefits when performing combined oxidative and non-oxidative dehydrogenationsbyperiodicoperationhavebeenbrieflyreviewed[ 13]. [Pg.355]

Itoh, N. and R. Govind, Combined oxidation and dehydrogenation in a palladium membrane, Ind. [Pg.319]

Any number of reactants may be considered, each of which can be transferred at a positive or negative rate. Positive rates cause mass to be added to the system at negative rates it is removed. Reactants may be minerals, aqueous species (in charge-balanced combinations), oxide components, or gases. Since the role of a... [Pg.11]

Fig. 23. Volume profile for the combined oxidative addition and reductive elimination reaction [PdMe2(bpy)] + Mel — [Pd(I)Me3(bpy)] — [Pd(I)Me(bpy)J + C2H6. Fig. 23. Volume profile for the combined oxidative addition and reductive elimination reaction [PdMe2(bpy)] + Mel — [Pd(I)Me3(bpy)] — [Pd(I)Me(bpy)J + C2H6.
Equation (16) notes that the difference in measured 5 Fe values for Fe(II)aq and ferrihydrite precipitate is equal to difference in the Fe(III)aq-ferrihydrite and Fe(III)aq-Fe(II)aq fractionation factors, assuming that the proportion of Fe(III)aq is very small (<5%). In cases where the proportion of Fe(III)aq ratio is significant (>5%), the isotopic effects of combined oxidation and precipitation may still be calculated using an incremental approach and Equation (12), along with the pertinent fractionations between components (Eqns. 14 and 17). [Pg.333]

This reaction again represents a combined oxidation and decarboxylation. [Pg.92]

Continued investigation revealed that the principal epoxidizing agents for combined oxidation of unsaturated compounds and aldehydes are not the corresponding peracids, but the radicals of acyl peroxides. [Pg.17]

For the combined oxidation processes, the effect of pH is even more complex. Experimental results have shown a steady increase in the reaction rate of micropollutants with increasing pH, as well as optima at various pH values. [Pg.120]

If the water consumes ozone very fast, in this case faster than transferred, a mass transfer limitation can occur. Ozone could already be consumed before the second oxidant is added. Then one cannot talk about combined processes, a pretreatment with ozone alone could be a possible solution before using combined oxidants. Even if ozone is not consumed before the addition of the second agent the role of transfer limitation should always be considered and investigated. [Pg.151]

Jochimsen J C, Jekel M (1996) Partial oxidation effects during the combined oxidative and biological treatment of separated streams of tannery wastewater, in Clausthaler Umwelt-Akademie Oxidation of Water and Wastewater, A Vogelpohl (Hrsg.), Goslar 20.-22. Mai 1996. [Pg.173]

Several deadly species of the genus Amanita produce colorless toxic octapeptides, the amani-tins.a b Two residues of glycine, one of L-isoleucine, one of the unusual L-dihydroxyisoleucine, one of L-asparagine, and one of L-hydroxyproline are present in a-amanitin. In the center a modified tryptophan residue has been combined oxidatively with an SH group of a cysteine residue. If the dihy-droxyisoleucine residue of a-amanitin is replaced with unhydroxylated leucine, the resulting compound, known as amanullin, is nontoxic. The LD50 for mice is 0.3 mg kg 1 and 50 g of fresh Amanita phalloides may be sufficient to kill a person. Arnan-itins act slowly, and it is impossible to kill mice in less than 15 h, no matter how high the dose. [Pg.1625]

The loss of an electron by M, M + + e, is the process of oxidation in electrochemistry. The electron is then accepted by an electrode of well defined potential, so that the oxidation potential Eox is the free energy of the reaction, as was seen in Figure 4.1. Similarly the reduction potential Ered is the energy of the reduction reaction, e.g. N + e - N. By definition the molecule, which is oxidized, is the donor (M in this case), and the molecule, which is reduced, is the acceptor. The electron transfer from M to N is therefore equivalent to the combined oxidation of the donor and reduction of the acceptor, so that the energy balance is... [Pg.98]

Reaction LXIH. Combined Oxidation and Redaction of Aromatic Aldehydes under the influence of Caustic Alkalis (Cannizzaro). (B., 14, 2394.)—The lower aliphatic aldehydes, except formaldehyde, are resinified by caustic alkali aromatic aldehydes, however, and some of the higher aliphatic aldehydes behave differently, two molecules smoothly interacting to give, by simultaneous oxidation and reduction, one molecule each of the corresponding acid and alcohol. [Pg.184]

A new ionic liquid, l-butyl-3-methylimidazolium tribromide can act as an oxidizing agent to convert alcohols to aldehydes and ketones.338 In the case of benzyl alcohols and diols, [Bmim][Br3] combines oxidizing and brominating properties in a one-pot synthesis of /3-bromoethyl esters. [Pg.42]

The reaction and separation synthesis approach of Section 5 has been adopted to the problem of activated sludge process design (83). The conventional designs as well as all novel schemes for combined oxidation/denitrification of wastewater are explored. The process is optimized using a novel methodology for optimal reaction/separation network synthesis, supplied with a comprehensive kinetic model (84). The activated sludge process is synthesized using the systematic... [Pg.449]

As we can see from Table III, 86% of the sulfur contained in all of the oxidation products resides in the soluble oxidation products even though this product fraction only represents 52% by weight of the combined oxidation products. This indicates that organic sulfur compounds have been preferentially depolymerized from the coal matrix and that this oxidative procedure may be a possible desulfurization process. [Pg.306]

Schwammlein K, Leitzke O. Field tests for the elimination of chlorinated hydrocarbon compounds in ground water by combined oxidation processes. Proceedings of 12th Ozone World Congress, Lille, France, 1995 325-336. [Pg.84]

Yamaguchi, K., Mizugaki,T., Ebitani, K. and Kaneda, K. (1999). Heterogeneous N-oxidation of pyridines using a combined oxidant of hydrogen peroxide and nitriles catalysed by basic hydrotalcites. New J. Chem. 23, 799. [Pg.323]

In the oxidative or reductive versions of the reaction types listed above the [nucleophile, electrophile] combination is not allowed instead we use [nucleophile, nucleophile] combinations oxidatively or [electrophile, electrophile] combinations reductively [R—E, Nu-], [C=C( J-), Nu-], [R—Nu, E+] and [C=C(<5+), E+]. This principle (Umpolung see Section 1) vastly increases the number of choices available for synthetic schemes, and particularly allows for short cuts in conventional ones. Thus, the synthesis of ArOH or ArCN from ArH normally requires four steps (18), whereas the... [Pg.91]


See other pages where Combined oxide is mentioned: [Pg.349]    [Pg.665]    [Pg.323]    [Pg.207]    [Pg.304]    [Pg.236]    [Pg.373]    [Pg.542]    [Pg.196]    [Pg.56]    [Pg.314]    [Pg.108]    [Pg.578]    [Pg.2517]    [Pg.149]    [Pg.10]    [Pg.173]    [Pg.13]    [Pg.35]    [Pg.320]    [Pg.180]    [Pg.32]    [Pg.49]   
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