Dipartimento di Chimica, Università di Torino, 10125 Turin, Italy.
Environ Sci Pollut Res Int. 2013 May;20(5):3224-31. doi: 10.1007/s11356-012-1242-0. Epub 2012 Oct 12.
The photocatalytic degradations of 4-chlorophenol (CP), 4-chloro-2-methylphenol (CMP), 4-chloro-3,5-dimethylphenol (CDMP) and 4-chloro-2-isopropyl-5-methylphenol (CIMP) were investigated in water and in simulated soil washing wastes containing Brij 35 (polyoxyethylene(23)dodecyl ether) in the presence of TiO2 dispersions. A neat inhibition of substrate decomposition proportional to their growing hydrophobicity was observed in the washing wastes for CP, CMP and CDMP, whereas CIMP showed a different behaviour. The mineralization of the organic chlorine of CP and CIMP was relatively fast and complete, whereas it was much slower for CMP and CDMP. Micellar solubilization and substrate adsorption onto the semiconductor play opposite roles on the degradation kinetics, and a breakpoint between the corresponding induced effects was evidenced when the pollutants become completely bound to the micellar aggregates.
在水相和含有 Brij 35(聚氧乙烯(23)十二烷基醚)的模拟土壤洗脱废水中,研究了 4-氯苯酚(CP)、4-氯-2-甲基苯酚(CMP)、4-氯-3,5-二甲基苯酚(CDMP)和 4-氯-2-异丙基-5-甲基苯酚(CIMP)在 TiO2 分散体存在下的光催化降解。在洗脱废水中,观察到 CP、CMP 和 CDMP 的底物分解呈与它们不断增加的疏水性成正比的明显抑制,而 CIMP 则表现出不同的行为。CP 和 CIMP 的有机氯的矿化相对较快且完全,而 CMP 和 CDMP 的矿化则要慢得多。胶束增溶和底物吸附在半导体上对降解动力学起着相反的作用,当污染物完全结合到胶束聚集体上时,证据表明存在相应诱导效应的转折点。