Ultrasonic and dielectric behaviour of binary systems of quinoline with methylene chloride, chloroform, carbon tetrachloride, benzene and cyclohexane

1992 ◽  
Vol 88 (15) ◽  
pp. 2197 ◽  
Author(s):  
Jagan Nath ◽  
M. Tevari

A calorimeter has been designed for measuring the heats of mixing of binary liquid systems, which eliminates the need to correct for changes in the composition of the vapour phase on mixing. Improved accuracy has thus been obtained. Heats of mixing have been measured for the three binary systems formed from the three components carbon tetrachloride, chloroform and methylene chloride, and also for the systems benzene + carbon tetrachloride and benzene + ethylene dichloride. Reports that the last system is ideal have been disproved.


1971 ◽  
Vol 49 (1) ◽  
pp. 74-77 ◽  
Author(s):  
M. Cowie ◽  
Harry Watts

The binary gaseous diffusion coefficients of air with methane, methyl chloride, methylene chloride, chloroform, and carbon tetrachloride at 298.2 °K and 1 atm have been determined. A simple diffusion cell was used, in which concentration changes of the diffusing gas were followed by infrared spectrophotometry.


1997 ◽  
Vol 136 (1-2) ◽  
pp. 307-314 ◽  
Author(s):  
L Simoiu ◽  
I Trandafir ◽  
M Pleniceanu ◽  
M Baniceru

1969 ◽  
Vol 52 (3) ◽  
pp. 526-532
Author(s):  
John H Onley ◽  
George Yip

Abstract An established method for chlorinated insecticides has been modified and extended to include substituted urea herbicides, some urea metabolites, and amitrole. Starting with an acetonitrile sample extract, chlorinated insecticides are removed by petroleum ether extraction for the usual cleanup and determination. The aqueous acetonitrile phase is next extracted with methylene chloride and carbon tetrachloride to isolate the urea compounds (chloroxuron, diuron, fenuron, fluometuron, linuron, metobromuron, monuron and neburon) and some of their metabolites. This combined extract is chromatographed on a MgO-cellulose-Florisil column from which two eluatcs are obtained: one contains the substituted urea herbicides, aniline metabolites, and one compound with the urea moiety and the second contains four compounds with the urea moiety. Both eluates are analyzed by thin layer chromatography. Finally, the aqueous acetonitrile extract is passed through a column of Amberlite IR-120 resin. Amitrole (3-AT), which is absorbed on the resin, is removed with NH4OH and determined by a colorimetric procedure. Recoveries of all compounds from samples fortified at 0.05–5 ppm ranged between 70 and 106%. Apparent limit of sensitivity was 0.05 ppm for both the substituted urea herbicides and their metabolites and for amitrole. Recoveries for the chlorinated insecticides at 0.005 ppm ranged between 76 and 104%.


1997 ◽  
Vol 31 (2) ◽  
pp. 219-228 ◽  
Author(s):  
Fei T. Mak ◽  
Sarita R. Zele ◽  
William J. Cooper ◽  
Charles N. Kurucz ◽  
Thomas D. Waite ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document