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Recovery of Riologieal Conversion Products Biological conversion produces that can be derived from solid wastes include compost, methane, various proteins and alcohols, and a variety of other intermediate organic compounds. The principal processes that have been used are reported in Table 25-64. Composting and anaerobic digestion, the two most highly developed processes, are considered further. The recovery of gas from landfills is discussed in the portion of this sec tion dealing with ultimate disposal. [Pg.2242]

Due to some stability concerns with the N-Cbz group of 8 at high temperatures, compound 25 was used as a model substrate for the reaction. Substrate 25 was irradiated for 2 min (internal temperature reached 185 °C) in a variety of solvents and all thermal reactions reached >95% conversion (Table 6.1). Both aprotic polar solvents (entries 6 and 9) and protic polar solvent (entry 7) gave poor assay yields of product 26. With nonpolar solvents (entry 10) such as o-xylene and xylenes, the rearrangement reaction provided the highest assay yield and proved to be the best solvent choice [9e],... [Pg.170]

Table 1 Conversion of Pyrylium Salts into Benzenoid Compounds... Table 1 Conversion of Pyrylium Salts into Benzenoid Compounds...
Reactions of Organic Fluorine Compounds Table 7. Conversion of Fluoroform to Bromotrifluoromethane... [Pg.371]

Table 1 Kinetic and thermodynamic parameters for the conversion of compound 4 into benzo-18-crown-6 in 99% DMSO at 298.0 K and in the presence of an excessive amount of templating alkali bromide53... Table 1 Kinetic and thermodynamic parameters for the conversion of compound 4 into benzo-18-crown-6 in 99% DMSO at 298.0 K and in the presence of an excessive amount of templating alkali bromide53...
Even so, you may occasionally come across an older formula given in U.S. customary units. Should you wish to convert from one to the other you will want to use the compound conversion chart found under Conversion Tables at the back of the book. This is because the figures are not directly interchangeable between U.S. customary and metric, because 1.0 liter of water does not exactly equal 32.0 oz. Therefore, they must be specially compounded to be equivalent. [Pg.165]

The following dry and liquid tables will help you to quickly make compound conversions.Any amount not found in one of the tables can be converted by using one of the compound conversion formulas given below. [Pg.326]

Table 2 Conversion of A-oxides to ring halo compounds. Table 2 Conversion of A-oxides to ring halo compounds.
A number of compounds of boron and aluminum (for example, B4H 10 and Al (CHi)e) have too few electrons to form the required number of ordinary covalent bonds. And, conversely, such compounds as PCI5 and SeF6 have more electrons than can be accommodated by octets around each of the atoms. Violations of the latter type, which must obviously occur when any atom forms more than four covalent bonds, are relatively common in compounds of elements beyond the first two eight-membered periods in the Periodic Table. [Pg.43]

Catalytic partial oxidation at very short contact times is a promising route to new chemicals and to catalytic destruction of volatile organic compounds. Conversions of the limiting reaction are >99% at residence times less than 1 millisecond, and low concentrations of undesired products are observed. The results discussed in this paper are summarized in Table 1 below. [Pg.498]

Table 8. Conversion yields obtained from organic phosphorus compounds... Table 8. Conversion yields obtained from organic phosphorus compounds...
Conversion of Model Compounds. Experimental data are presented in Table II. Two conversions are shown for each run. Total conversion represents the conversion to all products, while conversion to non-oxygenates represents conversion to all hydrocarbon, CO and HoO products. [Pg.282]

Table 11 Model compound conversion data 410 C, 1 atm., 1.0-1.1 WHSV, 20 min. reaction intervals HZSM-5 in Si02/Al203... Table 11 Model compound conversion data 410 C, 1 atm., 1.0-1.1 WHSV, 20 min. reaction intervals HZSM-5 in Si02/Al203...
If, for example, 2 mol of diamine is reacted until complete conversion (pcooH = 1) with a mol of dicarboxyUc acid (ro = 0.5), then the number-average degree of polymerization is X = 3, in accordance with equation (17-24), and the mass-average degree is Xw— 5, in accordance with equation (17-38). Following from Equation (17-40), however, the diamide will only be formed up to 25% by weight (w, = 0.25), so that the yield of this compound can only reach 25% of the theoretical formula molar conversion (Table 17-4). [Pg.113]

In naming chemical compounds the systematic lUPAC system is increasingly used in educational establishments. However in many areas of chemistry, e.g. natural products, trivial names are still far more important, as indeed they are in the chemical industry. Again it is desirable to be bilingual. To assist in this trivial names are used in this book, but the lUPAC name is usually given in brackets afterwards. A reference table for the two systems of naming compounds is also provided at the front of the book. Since only trivial names are used in the index in this book, this conversion table should be used to obtain the trivial name from its systematic counterpart. [Pg.4]

Table 6 Some volatile compounds conversion factors ... Table 6 Some volatile compounds conversion factors ...
D Eha Camacho et al. (2011) proposed a novel concept using an assisted electrochemical reaction to produce atomic hydrogen from water electrolysis for different heterorganic compounds conversion. The electrochemical reactor is divided into two compartments by a palladium membrane in which atomic hydrogen is absorbed and permeated. Organic sulfur in the oil can be desulfurized and transformed to H2S in the electrochemical compartment. In addition, Lam et al. (2012) recently presented a review of electrochemical desulfurization technologies for fossil fuels. Various electrodes and electrolytes that have been used for desulfurization accomphshed by oxidation, reduction, or both were summarized by Lam et al. in their paper. Some electrochemical desulfurization processes for transportation fuels were chosen for listing in Table 14.2. [Pg.406]

Nitriles contain the —C=N functional group We have already discussed the two mam procedures by which they are prepared namely the nucleophilic substitution of alkyl halides by cyanide and the conversion of aldehydes and ketones to cyanohydrins Table 20 6 reviews aspects of these reactions Neither of the reactions m Table 20 6 is suitable for aryl nitriles (ArC=N) these compounds are readily prepared by a reaction to be dis cussed m Chapter 22... [Pg.867]


See other pages where Conversion tables compound conversions is mentioned: [Pg.562]    [Pg.351]    [Pg.532]    [Pg.382]    [Pg.19]    [Pg.408]    [Pg.206]    [Pg.48]    [Pg.16]    [Pg.15]    [Pg.290]    [Pg.246]    [Pg.3]    [Pg.1244]    [Pg.509]    [Pg.8]    [Pg.143]    [Pg.320]    [Pg.1022]    [Pg.369]    [Pg.38]   
See also in sourсe #XX -- [ Pg.326 , Pg.327 , Pg.328 ]




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Compound table

Conversion compounds

Conversion tables

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