期刊
CHEMICAL ENGINEERING JOURNAL
卷 421, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.127728
关键词
Persulfate; Thermally activated; P-xylene; Process parameters; Mechanism
资金
- Fundamental Research Funds for the universities of Zhejiang Province [RFA2019011]
- Key Project of Zhejiang Province Natural Science Foundation [LZ17E080001]
- National Key R and D Program of China [2019YFC0214400]
The study demonstrates that the combination of wet scrubber and thermally activated persulfate can efficiently remove p-xylene, with a maximum removal efficiency of 78.5%. By adjusting the activation temperature and PS dosage, as well as controlling the gas flow rate and absorption solution pH, the removal efficiency of p-xylene can be optimized.
The coupling of wet scrubber with thermally activated persulfate (PS) for the removal of gaseous p-xylene was studied in the present work. The effects of process parameters (i.e., activation temperature, gas flow rate, PS dosage, and absorption solution pH) on p-xylene removal were studied. The removal efficiency increased with the activation temperature and PS dosage, while decreased with the increase of gas flow rate. The inhibition effect was observed when the pH of the reaction system was alkaline due to the existence of NH3(aq) resulting from ammonium translation. P-xylene was efficiently eliminated under the optimal conditions with a maximum removal efficiency of 78.5%. The most important radicals, namely, SO4 center dot- and HO center dot, were investigated by electron paramagnetic resonance, and the selectivity of SO4 center dot- was determined by quenching tests. HO center dot and SO4 center dot-oxidations accounted for 41.3% and 37.4% of the removal of p-xylene, respectively. The contribution of SO4 center dot- increased with the accumulation of H+. Moreover, the absorption solution reused via adding PS and it still showed perfect removal capacity for p-xylene at the end of each cycle. Finally, a possible degradation pathway of p-xylene was proposed based on the measurements of intermediates being detected in the gas and liquid phases.
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