Transformation of bromide and formation of brominated disinfection byproducts in peracetic acid oxidation of phenol

Chemosphere ◽  
2021 ◽  
pp. 132698
Author(s):  
Liang Meng ◽  
Jing Chen ◽  
Deyang Kong ◽  
Yuefei Ji ◽  
Junhe Lu ◽  
...  
1980 ◽  
Vol 60 (3) ◽  
pp. 541-548 ◽  
Author(s):  
M. SCHNITZER ◽  
D. A. HINDLE

Three humic and one fulvic acid were degraded by mild chemical oxidation with peracetic acid, with special emphasis on the effects of this type of oxidation on N-containing components. The different types of N that were considered were NH4+-N, amino acid-N, amino sugar-N, NO2−-N + NO3−-N, and by difference from total N, "unknown" N. The behaviour toward mild chemical oxidation of all four preparations was essentially similar: there were decreases in mino acid-N, amino sugar-N and "unknown" N, increases in NH4+-N, NO2−-N + NO3−-N with one material, and in N-gases. The "unknown" N was not inert. Between 16.6 and 59.1% of the latter appeared to be converted, as a result of mild chemical oxidation, to NH3 and N-gases which were expelled from the systems. The results presented provide an insight into what happens to N-containing humic components as a result of mild oxidation.


2011 ◽  
Vol 127 (3) ◽  
pp. 1107-1117 ◽  
Author(s):  
Colin Y. L. Woon ◽  
Brian C. Pridgen ◽  
Armin Kraus ◽  
Sina Bari ◽  
Hung Pham ◽  
...  

1949 ◽  
Vol 71 (6) ◽  
pp. 2248-2249 ◽  
Author(s):  
Chester J. Cavallito ◽  
Dorothy McKenica. Fruehauf

ChemInform ◽  
2005 ◽  
Vol 36 (30) ◽  
Author(s):  
Bu-Lan Wu ◽  
Zhao-Bin Chen

1970 ◽  
Vol 48 (7) ◽  
pp. 759-762 ◽  
Author(s):  
M. W. Roomi ◽  
C. Y. Hopkins

Oxidation of sterculic acid by aqueous alkaline permanganate gave 9,11-dioxononadecanoic acid. Oxidation of sterculic acid by peracetic acid gave a mixture of 9-oxononadec-10-enoic and 11-oxononadec-9-enoic acids. Acetolysis of malvalic acid gave a mixture of 8-hydroxy-9-methylene-heptadecanoic and 9-hydroxy-8-methylene-heptadecanoic acids. Seed oil of Pterospermum acerifolium Willd. (family Sterculiaceae) contained malvalic acid as its major cyclopropenoid component. It comprised about 16% of the total fatty acids.


1959 ◽  
Vol 37 (2) ◽  
pp. 366-369 ◽  
Author(s):  
Paul E. Gagnon ◽  
Brian T. Newbold

A series of dihalogenated and five tetrachloroazobenzenes were oxidized to the corresponding azoxy compounds by means of 30% hydrogen peroxide in glacial acetic acid, the reaction being carried out at about 60–70 °C, for 24 hoursAs expected, the yields, in general, obtained from azobenzenes containing substituents in the 2,2′-positions were lower than those from compounds having substituents in the 3,3′- and 4,4′-positions, which gave very good results.


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