Treatment of water contaminated with diphenolic acid by gamma radiation in the presence of different compounds

被引:38
作者
Abdel Daiem, Mahmoud M. [1 ]
Rivera-Utrilla, Jose [1 ]
Ocampo-Perez, Raul [1 ]
Sanchez-Polo, Manuel [1 ]
Lopez-Penalver, Jesus J. [1 ]
机构
[1] Univ Granada, Dept Inorgan Chem, Fac Sci, E-18071 Granada, Spain
关键词
Diphenolic acid; Gamma radiation; Additives; Degradation; ADVANCED OXIDATION PROCESSES; BISPHENOL-A; TEMPERATURE-DEPENDENCE; RADIOLYTIC DEGRADATION; AQUEOUS-SOLUTION; VIBRIO-FISCHERI; RATE CONSTANTS; PHARMACEUTICALS; IRRADIATION; POLYESTERS;
D O I
10.1016/j.cej.2012.12.069
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The elimination of diphenolic acid (DPA) from contaminated water is an urgent challenge. The aim of this study was to investigate DPA degradation by gamma radiation, studying the influence of the dose rate, initial DPA concentration, solution pH, the presence of O-2, and the presence of different additives (e.g., Br-, Cl-, CO32-, NO2-, NO3-, and SON. A further objective was to study the effect of the water matrix (ultrapure water, surface water, and wastewater) and the variation in total organic carbon and toxicity as a function of absorbed dose. Results obtained showed that: gamma radiation was effective to remove DPA from aqueous solution; the dose constant was slightly dependent on the dose rate; and the solution pH had a major influence on DPA degradation, which was highest at pH 7. DPA degradation was reduced in the presence of Br-, Cl-, CO32-, NO2-, NO3-, and SO42- and was lower with higher concentrations of these species, largely due to their competition with DPA for the reactive radicals generated, especially Ha. Lower yield of DPA decomposition were obtained with wastewater and surface water than with ultrapure water due to the presence of organic matter and HCO3-, Cl-, SO42-, and NO3- ions, which react with the reactive radical species (HO., H-. and e(aq)(-)). The TOC and toxicity of the medium decreased during DPA degradation in all water types studied. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:371 / 379
页数:9
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