Reactive radical study using the polyvinyl alcohol–potassium iodide solution as a new chemical probe

2021 ◽  
Author(s):  
Hiroto Matsuura ◽  
Nguyen Tran Trung ◽  
Bounyang Ouanthavinsak ◽  
Jin Sakamoto ◽  
Yuichiro Takemura ◽  
...  
2016 ◽  
Vol 38 (2) ◽  
pp. 67-70
Author(s):  
A. V. Mamaenko ◽  
A. O. Samsoni Todorov ◽  
O. V. Zui ◽  
V. A. Yaremenko ◽  
V. V. Goncharuk

1993 ◽  
Vol 76 (2) ◽  
pp. 292-296 ◽  
Author(s):  
Kumiko Sasaki ◽  
Keiji Kijima ◽  
Mitsuharu Takeda ◽  
Shigeo Kojima

Abstract A simple specific determination method was developed for ethylene oxide (EO) and ethylene chlorohydrin (ECH) in cosmetics and surfactants. EO is desorbed from samples by using a nitrogen stream and absorbed into acidic potassium iodide solution, where it is converted to ethylene iodohydrin (EIH). Any remaining ECH in the samples is converted to EO by the addition of sodium hydroxide, and the desorption procedure is repeated with a fresh acidic potassium iodide absorbing solution. EIH is extracted with benzene and determined by gas chromatography with electron capture detection. EO and ECH contents in the samples are calculated from EIH results. Recoveries from water and shampoo samples were 70.3 ± 5.4 and 58.9 ± 1.2%, respectively, for EO and 66.3 ± 4.0 and 64.5 ± 4.6%, respectively, for ECH. Detection limits in 0.2-2.0 g samples were in the 0.005-0.03 μg/g range for EO and 0.01-0.07 μg/g for ECH. High levels of EO (30-394 μg/g as ECH) were found in 5 of 18 polyoxyethylated surfactant samples, but only small amounts (0.07-4.0 μg/g) of ECH were detected in the samples. EO was not detected in cosmetic samples tested, but ECH was present in small quantities (≤1.11 μg/g).


1970 ◽  
Vol 48 (18) ◽  
pp. 2847-2852 ◽  
Author(s):  
Digby D. MacDonald ◽  
G. A. Wright

Dissolution of bismuth metal by tri-iodide ion in acidified potassium iodide medium has been studied using a rotating disc technique. The rate constant for the dissolution process, kT, in solutions 0.5 M in potassium iodide at 25.0 °C has been shown to be related to the square root of the disc angular velocity, ω, by the following expression[Formula: see text]The activation energy for this reaction was found to be 4.7 kcal mole−1. These data clearly establish that the rate of dissolution is determined by the rate at which tri-iodide ion is transported to the metal surface. In solutions of [KI] = 0.10 M, however, the rate determining step appears to involve diffusion of tri-iodide ion through a layer of BiI3 which forms on the bismuth metal surface as the reaction proceeds.


2008 ◽  
Vol 20 (20) ◽  
pp. 2265-2270 ◽  
Author(s):  
Mei-Hsin Chiu ◽  
Jyh-Myng Zen ◽  
Annamalai Senthil Kumar ◽  
Dhananjayan Vasu ◽  
Ying Shih

AIHAJ ◽  
1992 ◽  
Vol 53 (10) ◽  
pp. 672-672 ◽  
Author(s):  
M. Hekmat ◽  
P. Fung ◽  
R. Smith

1964 ◽  
Vol 10 (7) ◽  
pp. 575-580 ◽  
Author(s):  
Lee Kum-Tatt ◽  
P C Leong

Abstract A simple method for the determination of ascorbic acid in urine was developed. The method is based on the quantitative reduction of mercuric chloride to mercurous chloride at pH 3.5-5.0. The insoluble mercurous chloride was separated by centrifugation, dissolved in excess standard iodine-potassium iodide solution and back-titrated with standard sodium thiosulphate. The method has precision, and as little as 1.0 mg. of ascorbic acid per 100 ml. of urine can be determined with an accuracy of ± 3%. Common substances found in urine do not interfere.


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