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Chloride carbonation

Margottin-Maclou M, Doyennette L and Henry L 1971 Relaxation of vibrational energy in carbon monoxide, hydrogen chloride, carbon dioxide and nitrous oxide App/. Opt. 10 1768-80... [Pg.3015]

JiVith ammoniacal or hydrochloric acid solution of copper(I) chloride, carbon monoxide forms the addition compound CuCl. CO. 2H2O. This reaction can be used to quantitatively remove carbon monoxide from gaseous mixtures. [Pg.180]

Phosphoryl chloride Carbon disulflde, A,A-dimethylformamide, 2,5-dimethylpyrrole, 2,6-dimethyl-pyridine 1-oxide, dimethylsulfoxide, water, zinc... [Pg.1211]

Fig. 3J0 Plot of cumulative pore volume against logarithm of r the effective pore radius, (o) For charcoal AY4 A by mercury intrusion O by capillary condensation of benzene, (b) For zinc chloride carbon AYS A by mercury intrusion O by capillary condensation of benzene x by capillary condensation of benzene, after mercury intrusion followed by distillation of mercury under vacuum at temperature rising to 350°C. (Courtesy... Fig. 3J0 Plot of cumulative pore volume against logarithm of r the effective pore radius, (o) For charcoal AY4 A by mercury intrusion O by capillary condensation of benzene, (b) For zinc chloride carbon AYS A by mercury intrusion O by capillary condensation of benzene x by capillary condensation of benzene, after mercury intrusion followed by distillation of mercury under vacuum at temperature rising to 350°C. (Courtesy...
Ma.nga.nese. Commonly used manganese fertilizer materials are manganous and manganic sulfates, chlorides, carbonates, oxides, frits, and chelates. Soil appHcation rates range from about 2 to 150 kg/hm of Mn. [Pg.242]

Coal ash is derived from the mineral content of coal upon combustion or utilization. The minerals are present as discrete particles, cavity fillings, and aggregates of sulfides, sulfates, chlorides, carbonates, hydrates, and/or oxides. The key ash-forming elements and compounds are (4,5) ... [Pg.252]

NOTE - Petrochemical plants also generate significant amounts of solid wastes and sludges, some of which may be considered hazardous because of the presence of toxic organics and heavy metals. Spent caustic and other hazardous wastes may be generated in significant quantities examples are distillation residues associated with units handling acetaldehyde, acetonitrile, benzyl chloride, carbon tetrachloride, cumene, phthallic anhydride, nitrobenzene, methyl ethyl pyridine, toluene diisocyanate, trichloroethane, trichloroethylene, perchloro-ethylene, aniline, chlorobenzenes, dimethyl hydrazine, ethylene dibromide, toluenediamine, epichlorohydrin, ethyl chloride, ethylene dichloride, and vinyl chloride. [Pg.57]

Note Maximum ambient levels for ethylene oxide are 0.3 ppb at the plant fence. Maximum total emissions of the VOCs acetaldehyde, acrylic acid, benzyl chloride, carbon tetrachloride, chlorofluorocarbons, ethyl acrylate, halons, maleic anhydride, 1,1,1-trichlorethane, trichloroethylene, and trichlorotoluene are 20 mg/Nnf. Maximum total heavy metal emissions are 1.5 mg/Nnf. [Pg.60]

Chlorkohlen-oxyd, n. carbonyl chloride, -oxyd-ather, m. ethyl chloroformate. -saure, /. chlorocarbonic acid (chloroformic acid, CICOOH). -sMureamtd, n. chlorocarbonyl amide (carbamyl chloride, H2NCOCI). -stoff, m. carbon chloride, carbon tetrachloride (sometimes with the adj. vierfach). [Pg.91]

The extrapolation to zero pressure may be effected if two measurements of pv at small pressures have been made, provided the gas satisfies equation (1). If this is not the case (e.g., hydrogen chloride, carbon dioxide), a number of points must be fixed on the curve, especially in the low pressure region. [Pg.157]

Example 2. Vinviidene Chloride Isobutylene Copolymer. The next example is for the carbon-13 spectrum of copolymer vinylidene chloride isobutylene. Figure 5 shows the full spectrum and the peak assignment listing for the non-protonated vinylidene chloride carbon in the 84-92 ppm range. Triad assignments were made (Crowther, M. W., 1987, Syracuse University, unpublished data) using the two-dimensional COLOC (20) experiment. There are ten v-centered pentads representing different environments for the vinylidene chloride carbon. The i represents the non-protonated carbon in the isobutylene polymer unit. [Pg.166]

Biphilicylides 117 can enter in cyclocondensations with carboxylic acid chlorides, carbon disulfide, and acyl isothiocyanates [126]. Certain corresponding heterocychc products 118 obtained are described for the first time (Y =N(CO)Ph Y=S) and are precursors of the new l-(2-phenylthiazol-5-yl)-5-phenyltetrazole 119 (Scheme 33). [Pg.67]

The solubility parameters of PCL are 20.8 and 20.4 jl/2.cm"2 2 when calculated using the parameters of Fedors and Hoy, respectively (58). PCL is soluble in a number of solvents at room temperature, including THF, chloroform, methylene chloride, carbon tetrachlornie, benzene, toluene, cyclohexanone, dihydropyran, and 2-nitropropane. [Pg.82]

Breslow and co-workers have found that cosolvents such as ethanol increase the solubility of hydrophobic molecules in water and provide interesting results for nucleophilic substitutions of phenoxide ions by benzylic chlorides carbon alkylation occurs in water but not in nonpolar organic solvents, and it is observed only when the phenoxide has at least one methyl substituent (ortho, meta, or para). This has been discussed in Chapter 6 (Section 6.4.2). [Pg.208]

As noted above, there is experimental evidence to indicate that the carbonyl groups of (vinyl chloride)-(carbon monoxide) copolymers are effective sensitizers for the photodegradation of these materials (9,10,11). A reasonable sensitization mechanism can be formulated for this system on the basis of the information now on hand. [Pg.201]

Fundamentally, O-esters of N-hydroxy-2-thiopyridone are photo-lyzed in the presence of an excess of white phosphorus in a methylene chloride/carbon disulfide medium. On solvent removal, hydrolysis, and oxidation with hydrogen peroxide, good yields of phosphonic acids (Figure 2.10) bearing the carbon functionality of the parent acid are isolated. [Pg.32]

During the reflux period, gases are continuously evolved these apparently are hydrogen chloride, carbon dioxide, ethyl acetate, and possibly ethyl chloride. The reaction should be run in a hood, or the gases should be trapped.8... [Pg.31]

PolyCvinyl fluoride) monomer, 20 586 PolyCvinylidene chloride) carbon,... [Pg.748]

The analogous hydroxylation of alkynes to produce ketones is enhanced by the co-catalytic effect of Aliquat and platinum(IV) chloride-carbon monoxide [3] it is assumed that HPtCI(CO) is the active hydration species. C-S and C-Br bonds are cleaved under the reaction conditions. [Pg.116]

Bromine (dry gas) Bromine (liquid) Bromobenzene Butanol Butyl acetate Butylamine Butylchloride Butyric acid Calcium chloride Carbon tetrachloride Castor oil Cellosolve Cellosolve acetate Chlorine (dry gas) Chlorine water Chloroacetic acid Chlorobenzene Chloroform Chlorosulfonic acid Chromic acid Citric acid Colza oil Copper sulfate Cyclohexane Cyclohexanol Cyclohexanone... [Pg.511]

Synonyms AI3-04705 Benzinoform Carbona Carbon chloride Carbon tet Caswell No. 164 CCRIS 123 EINECS 200-262-8 ENT 4705 ENT 27164 EPA pesticide chemical code 016501 Fasciolin Flukoids Freon 10 Halon 1040 Methane tetrachloride Necatorina Necatorine NSC 87063 Perchloromethane R 10 RCRA waste number U211 Tetrachloormetaan Tetrachloro-carbon Tetrachloromethane Tetrafinol Tetraform Tetrasol UN 1846 Univerm Vermo-estricid. [Pg.258]

Photolysis of an aqueous solution containing chloroform (314 pmol) and the catalyst [Pt(cohoid)/Ru(bpy) /MV/EDTA] yielded the following products after 15 h (mol detected) chloride ions (852), methane (265), ethylene (0.05), ethane (0.52), and unreacted chloroform (10.5) (Tan and Wang, 1987). In the troposphere, photolysis of chloroform via OH radicals may yield formyl chloride, carbon monoxide, hydrogen chloride, and phosgene as the principal products (Spence et al., 1976). Phosgene is hydrolyzed readily to hydrogen chloride and carbon dioxide (Morrison and Boyd, 1971). [Pg.295]

Photolytic. Reported photooxidation products via OH radicals include formyl chloride, carbon monoxide, hydrogen chloride, and phosgene (Spence et al., 1976). In the presence of water, formyl chloride hydrolyzes to HCl and carbon monoxide, whereas phosgene hydrolyzes to hydrogen chloride and carbon monoxide (Morrison and Boyd, 1971). [Pg.744]

Uses Coolant and refrigerant herbicide and fumigant organic synthesis-methylating agent manufacturing of silicone polymers, pharmaceuticals, tetramethyl lead, synthetic rubber, methyl cellulose, agricultural chemicals and nonflammable films preparation of methylene chloride, carbon tetrachloride, chloroform low temperature solvent and extractant catalytic carrier for butyl rubber polymerization topical anesthetic fluid for thermometric and thermostatic equipment. [Pg.745]

Miscible with many organic chlorinated solvents including methylene chloride, carbon tetrachloride, chloroform, trichloroethylene, 1,1,1-trichloroethane, 1,1,2-trichloroethane, and 1,1,2,2-tetrachloroethane... [Pg.1035]


See other pages where Chloride carbonation is mentioned: [Pg.437]    [Pg.41]    [Pg.311]    [Pg.164]    [Pg.104]    [Pg.307]    [Pg.220]    [Pg.27]    [Pg.29]    [Pg.210]    [Pg.274]    [Pg.359]    [Pg.247]    [Pg.660]    [Pg.406]    [Pg.204]    [Pg.92]    [Pg.26]    [Pg.1011]    [Pg.36]    [Pg.105]    [Pg.105]    [Pg.15]   
See also in sourсe #XX -- [ Pg.89 ]




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Acyl chlorides triphenylphosphine, carbon tetrachloride

Aluminum chloride-carbon disulfide

Ammonium carbonate chloride

Anode Processes on Carbon in Chloride Melts with Dissolved Oxides

Calcium carbonate, chloride

Calcium carbonate-ammonium chloride

Calcium chloride potassium carbonate

Calcium chloride sodium carbonate

Carbon carbonyl chloride

Carbon chloride

Carbon dioxide Cyanogen chloride

Carbon dioxide chloride solutions

Carbon monoxide chloride effect

Carbon monoxide methylene chloride metabolized

Carbon monoxide reaction with copper chloride

Carbon tetra-chloride

Carbon thionyl chloride

Carbon zinc chloride, primary

Carbon, acids chloride

Carbon-heteroatom bonds palladium©) chloride

Carbon-hydrogen bonds chloride dimer

Carbon-nitrogen bonds palladium©) chloride

Carbonation, chloride penetration and corrosion of reinforcement

Carbonic acid anhydrides chloride

Carbonic chloride esters

Chloride ions with carbon steels

Cuprous chloride dimethyl carbonate

From Chlorides, Oxalates, Carbonates, Nitrates

From carbon monoxide reaction with Group chlorides

Interaction of Carbon with Molten Salts-Chloride-Carbonate Melts

Lead, carbonate chlorid

Non-carbonated Concrete without Chlorides

Palladium chloride on carbon

Phosphate, chloride, carbonate and sulphate

Poly(vinyl chloride-co-carbon

Polyvinyl chloride calcium carbonate

Polyvinyl chloride, mechanisms carbonization

Potassium carbonate chloride

Propagation Time for Carbonation- (and Chloride)-induced Corrosion

Sodium carbonate in preparation acid chloride

Sodium carbonate reaction with barium chloride

Sodium chloride nitrate solution, carbon

Tosyl chloride/potassium carbonate

Uranyl ammonium carbonate chloride

Vinyl chloride carbon-centered radicals

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