Effects of mild thermal pre-treatment combined with H2O2 addition on waste activated sludge digestibility

被引:10
|
作者
Gonzalez, Adrian [1 ]
van Lier, Jules B. [1 ]
de Kreuk, Merle K. [1 ]
机构
[1] Delft Univ Technol, Fac Civil Engn & Geosci, Dept Water Management, Sanit Engn Sect, Stevinweg 1, NL-2628 CN Delft, Netherlands
关键词
Apparent viscosity; Catalase activity; Cationic polymer; Hydroxyl radicals; Low-temperature pre-treatment; Non-ideal mixing; ENHANCED ANAEROBIC-DIGESTION; HYDROGEN-PEROXIDE; SEWAGE-SLUDGE; PROTEIN OXIDATION; MICROWAVE-H2O2; PRETREATMENT; RHEOLOGICAL PROPERTIES; RADICAL FORMATION; FENTON REACTION; ACID; DEWATERABILITY;
D O I
10.1016/j.wasman.2022.01.017
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The pre-treatment of waste activated sludge (WAS) has become more common since it often results in improved bioconversion to methane, in both rate and extent. However, thorough insights on the possible effects and mechanisms of mild pre-treatment techniques, such as temperatures < 100 degrees C combined with the addition of H2O2, are still limited. This study reports the effects of the addition of 5-30 mgH(2)O(2)/g TS and its interaction with thermal pre-treatment at 70 degrees C on methane production, using WAS as the substrate. It was found that the addition of H2O2 increased the methane production rate, coinciding with a decrease in apparent viscosity of WAS, which probably improved mass transfer under non-ideal mixing conditions. While H2O2 solubilized proteins and carbohydrates and mineralized a small fraction of the humic substances in WAS, these biochemical transformations did not suffice to explain the observed extent and rate of methane production. A decreased particle size, the presence of Fenton's reagent, and the presence of cationic polymers in the WAS were discarded as the reasons for the observed decrease in apparent viscosity. It was concluded that the pre-treatment conditions applied in the present study might be a strategy to enhance mixing conditions in full-scale anaerobic digesters.
引用
收藏
页码:163 / 172
页数:10
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