Vapour-phase hetero-association of trifluoroacetic acid with acetic acid

Author(s):  
Chii Ling ◽  
Sherril D. Christian ◽  
Harold E. Affsprung ◽  
Robert W. Gray
1986 ◽  
Vol 51 (1) ◽  
pp. 194-205 ◽  
Author(s):  
Ivona Malijevská ◽  
Marie Sýsová ◽  
Dagmar Vlčková

Vapour-liquid equilibrium was measured in the systems acetic acid-propionic acid and acetic acid-trifluoroacetic acid at normal pressure. Special emphasis has been laid on the correct expression of the P-V-T behaviour in the vapour phase and the analysis of the data obtained.


1964 ◽  
Vol 47 (5) ◽  
pp. 801-803 ◽  
Author(s):  
Peter John Andrellos ◽  
George R Reid

Abstract Three confirmatory tests have been devised to identify aflatoxin B±. Portions of the isolated toxin are treated with formic acid-thionyl chloride, acetic acid-thionyl chloride, and trifluoroacetic acid, respectively, and aliquots of the three fluorescent reaction products are spotted on thin-layer chromatography plates. Standards treated with each of the three reagents, plus an untreated standard, are spotted on the same plate, and after development the spots are compared under ultraviolet light.


2007 ◽  
Vol 111 (31) ◽  
pp. 9270-9280 ◽  
Author(s):  
Toshiyuki Takamuku ◽  
Yasuhiro Kyoshoin ◽  
Hiroshi Noguchi ◽  
Shoji Kusano ◽  
Toshio Yamaguchi

2018 ◽  
Vol 63 (1) ◽  
pp. 170-178 ◽  
Author(s):  
László Kiss

In this article, the feasibility of the CuxS modified carbon microdisc electrode was examined by exposure to four different volatile organic compounds (2-propanol, acetic acid, ethyl acetate and n-butylamine) directly in their vapour phase using cyclic voltammetry and amperometry. The performance of the modified microdisc was compared with the bare carbon microdisc (30 μm in diameter) which was involved in a narrow-gap cell. By using both methods high current increase was observed for 2-propanol with the modified electrode and its sensitivity was sufficiently higher than with the bare electrode. The modified electrode showed lower current signals in case of acetic acid and n-butylamine. The latter formed a condensation layer at the interelectrode gap. Neither the bare nor the modified electrode was sensitive to ethyl acetate.


1995 ◽  
Vol 36 (22) ◽  
pp. 3945-3948 ◽  
Author(s):  
Jan Bergman ◽  
Eva Koch ◽  
Benjamin Pelcman

2009 ◽  
Vol 17 (1) ◽  
pp. 123-131 ◽  
Author(s):  
Tao Lu ◽  
Xiangdong Yao ◽  
Max Gao Qing Lu ◽  
Yinghe He

1967 ◽  
Vol 45 (1) ◽  
pp. 11-16 ◽  
Author(s):  
G. A. Latrèmouille ◽  
A. M. Eastham

Isobutene reacts readily with excess trifluoroacetic acid in ethylene dichloride solution at ordinary temperatures to give t-butyl trifluoroacetate. The rate of the reaction is given, within the range of the experiments, by the expression d[ester]/dt = k[acid]2[olefin], and the apparent activation energy is about 6 kcal/mole. The rate of addition is markedly dependent on the strength of the reacting acid and is drastically reduced in the presence of mildly basic materials, such as dioxane. The boron fluoride catalyzed addition of acetic acid to 2-butene can be considered to follow a similar rate law, i.e. d[ester]/dt = k[acid·BF3]2[olefin], but only if some assumptions are made about the position of the equilibrium [Formula: see text]since only the 1:1 complex is reactive.


Sign in / Sign up

Export Citation Format

Share Document