Polymerization of methyl methacrylate initiated by tert-butyl hydroperoxide-sulphuric acid-acetone system

1984 ◽  
Vol 49 (2) ◽  
pp. 404-409 ◽  
Author(s):  
Jiří Pavlinec ◽  
Milan Lazár

The radical polymerization of methyl methacrylate may be efficiently initiated by tert-butyl-hydroperoxide at 40°C and lower, deep below the temperatures of spontaneous hydroperoxide decomposition, when sulphuric acid simultaneously with ketones is used as the activator of peroxide decomposition. The initial reaction rate depends on concentration of initiator components, the exponents with regard to tert-butyl hydroperoxide, sulphuric acid and acetone being 0.25, 0.5 and 0.5, respectively. Water retards the hydroperoxide decomposition very efficiently and the polymerization rate is inversely proportional to the square root of water concentration in the system. Within the concentration range of hydroperoxide (1. 10-3 - 3. 10-2 mol dm-3), sulphuric acid 2.62 . 10-2 mol dm-3 and acetone 0.2 mol dm-3 the observed initial polymerization rate varies from 14.4%/hour to 34.5%/hour at 40°C. The concentration of water, introduced into the system by the polymerization components, was 0.05% in all cases. The activating effect of ketones upon the acid catalyzed hydroperoxide decomposition is accounted for by the formation of ketone-H2SO4 adduct that facilities the decomposition of hydroperoxide.

2016 ◽  
Vol 56 (2) ◽  
pp. 171-174 ◽  
Author(s):  
Kh. E. Kharlampidi ◽  
N. M. Nurullina ◽  
N. N. Batyrshin ◽  
V. I. Anisimova ◽  
I. A. Suvorova

2021 ◽  
Vol 4 (2) ◽  
pp. 23-27
Author(s):  
O. I. Makota ◽  
◽  
L. P. Oliynyk ◽  
Z. М. Komarenska ◽  
◽  
...  

Catalytic ability of tungsten compounds in the reaction of hydroperoxide epoxidation of 1- octene and tert-butyl hydroperoxide decomposition was investigated. It is shown that the nature of ligand has significant effect on the catalytic activity of tungsten compounds in these reactions. It is established that boride and silicide of tungsten are the best choice for epoxidation reaction, whereas tungsten carbide exhibits poor activity. Tungsten boride is also the most active in the hydroxide decomposition reaction.


1977 ◽  
Vol 55 (10) ◽  
pp. 1644-1652 ◽  
Author(s):  
Joseph Hector Bernard Chenier ◽  
James Anthony Howard ◽  
John Charles Tait

The initial reaction of cupric dialkyldithiophosphates and dialkyldithiocarbamates with tert-butyl hydroperoxide and α-cumyl hydroperoxide is a free radical chain process. Initiation is achieved by a redox reaction between the complex and the hydroperoxide to give alkoxy and alkylperoxy radicals. The alkoxy radicals then abstract a hydrogen from excess hydroperoxide to give alkylperoxy radicals. The cupric complexes are converted to copper sulphate by reaction with peroxy radicals while the hydroperoxide is reduced to alcohol. About 5 mol of hydroperoxide are decomposed by each mole of complex. The decomposition of tert-butyl hydroperoxide then stops whereas complete destruction of α-cumene hydroperoxide occurs by a heterogeneous ionic reaction.The kinetics of the initial reaction are second-order for both complexes. The dithiophosphate reaction is first-order in each reactant while the dithiocarbamate reaction is zero-order in the complex concentration and second-order in the hydroperoxide concentration. Simple kinetics, however, only hold for the initial rates of complex disappearance. Total dithiophosphate decomposition exhibits three stages, an initial fast reaction followed by an induction period and a rapid third stage. The concentration–time profile for dithiocarbamate decomposition is quite different and the overall rate of reaction in some instances increases as the complex concentration decreases.


2010 ◽  
Vol 35 (3) ◽  
pp. 345-348 ◽  
Author(s):  
Yuriy Trach ◽  
Oksana Makota ◽  
Jadwiga Skubiszewska-Zięba ◽  
Tadeusz Borowiecki ◽  
Roman Leboda

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