Quantitative Determination of Carbon Disulfide In Presence of Carbon Tetrachloride by Use of Dead-Stop End Point

1945 ◽  
Vol 17 (9) ◽  
pp. 563-564 ◽  
Author(s):  
Richard L. Bishop ◽  
E. Louise Wallace
1953 ◽  
Vol 26 (1) ◽  
pp. 251-256 ◽  
Author(s):  
Lewis T. Milliken

Abstract A procedure is recommended in which small amounts of copper in rubber can be measured quantitatively by determining the depth of color of a copper carbamate complex in a carbon tetrachloride solution. The complex is formed in an alkaline solution prepared from an acid extract of the rubber ashed at 550° C. This procedure yields results which are as reliable as those obtained by the more tedious and time-consuming procedures involving the wet-oxidation process which are at present recommended by standardizing organizations. The use of an organic solution rather than an aqueous suspension gives better reproducibility, permits easier use of a photometer, and reduces the interference due to iron by a factor of ten.


1960 ◽  
Vol 33 (4) ◽  
pp. 1062-1067
Author(s):  
A. L. Klebanskiĭ ◽  
L. P. Fomina

Abstract 1. Investigation of the process of radical dissociation of TETD in carbon tetrachloride indicates that at 145° thiuram radicals are formed which react with the carbon tetrachloride to form (C2H5)2N—C‖S—SCl and CS2. 2. A quantitative determination of the products of the base-influenced dissociation of TETD was carried out. A kinetic investigation of this reaction, in which initiator (K2S2O3) and inhibitor (PBNA) were shown to have no velocity effect whatever, indicates that the process is an ionic one. 3. It is shown that in the reaction of TETD with diethylamine, one of the reaction products appears to be diethylammonium diethyldithiocarbamate.


1936 ◽  
Vol 8 (4) ◽  
pp. 260-263 ◽  
Author(s):  
John C. Olsen ◽  
Henry F. Smyth ◽  
George E. Ferguson ◽  
Leopold Scheflan

1960 ◽  
Vol 6 (4) ◽  
pp. 327-331 ◽  
Author(s):  
Horace W Gerarde ◽  
Paul Skiba

Abstract A photoelectric colorimetric method is described for the quantitative determination of kerosine in blood. The procedure involves hemolysis of 5 ml. of the sample followed by extraction of the kerosine with carbon tetrachloride. The extract is reacted with a formaldehyde- sulfuric acid reagent to produce a characteristic color. The intensity of this color is measured photometrically, and the concentration of kerosine is determined by reference to a previously prepared calibration curve. Concentrations as low as 10 ppm can be conveniently determined.


1970 ◽  
Vol 53 (4) ◽  
pp. 742-746
Author(s):  
Bernadette Malone

Abstract A method is described for determination of residues of the fumigants methyl bromide, carbon disulfide, chloroform, ethylene dichloride, carbon tetrachloride, and ethylene dibromide in cereal grains. Whole or ground grain is boiled in an acid medium, and the volatile fumigants are dried and collected in cold solvent. Residues are determined by analyzing aliquots of the collected solution by electron capture GLC. Recoveries range from 59 to 105%. Extraction appears to be complete in the 2 hr boiling period specified. An unexplained conversion of carbon tetrachloride to chloroform is described.


1986 ◽  
Vol 69 (6) ◽  
pp. 990-998
Author(s):  
David L Heikes ◽  
Marvin L Hopper

Abstract A method developed for the determination of 1,2-dibromoethane in whole grains and grain-based products has been modified and expanded to include 8 other fumigants. Samples are stirred with water and purged with nitrogen for 0.5 h in a water bath at 100°C. The fumigants are collected on a trap composed of Tenax TA and XAD-4 resin, eluted with hexane, and determined by gas chromatography (GC) using electron capture detection or Hall electrolytic conductivity detection. Flame photometric detection in the sulfur mode is used to determine carbon disulfide. Thick-film, wide-bore capillary columns were used exclusively in both the determination and confirmation of the halogenated fumigants. The higher levels of fumigants are also confirmed by full scan GC/mass spectrometry. Samples are analyzed for carbon disulfide, methylene chloride, chloroform, 1,2-dichIoroethane, methyl chloroform, carbon tetrachloride, trichloroethylene, 1,2-dibromoethane, and tetrachloroethylene. A total of 25 whole grains, milled grain products, and intermediate grain-based foods analyzed by this method contained fumigant levels up to 51 ppm (carbon tetrachloride in wheat). Recoveries from fortified samples ranged from 82 to 104%. Chromatograms from this purge and trap method are clean, so that low parts per billion and sub-parts per billion levels can be quantitated for the halogenated analytes. The quantitation level for carbon disulfide is 12 ppb.


1948 ◽  
Vol 21 (4) ◽  
pp. 830-834
Author(s):  
P. P. Kobeko ◽  
E. K. Moskvina

Abstract 1. It has been found that synthetic rubber does not precipitate from a solution of dichloromethane by the addition of Wijs reagent, whereas natural rubber does precipitate under the same conditions. The reverse relation occurs with carbon disulfide as solvent. 2. A method has been developed for the determination of the unsaturation of butadiene rubber in solution in dichloromethane by the use of Wijs reagent. 3. It has been demonstrated that, by the use of a solution of iodine chloride in carbon tetrachloride, the reaction with rubber is complicated by the hydrolysis of iodine chloride during titration, but not by the substitution of hydrogen by halogen nor by the hydrolysis of the rubber-halogen addition product. 4. The possibility of obtaining accurate values for unsaturation by a calculation of this hydrolysis is demonstrated. 5. Two methods have been developed for the determination of the unsaturation of natural and butadiene rubbers.


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