Applied Physicochemical Processes, Universidad de Antioquia, Carrera 53 # 61-30, Medellín, Colombia.
Water Res. 2012 Mar 15;46(4):1198-206. doi: 10.1016/j.watres.2011.12.028. Epub 2011 Dec 20.
This study shows the effect of pH on the photocatalytic degradation of natural organic matter (NOM). The experiments were carried out in batch reactor (a solar UV-light simulator) with Degussa P-25 titanium dioxide (TiO2). The NOM degradation was followed by size-exclusion chromatography for dissolved organic carbon (DOC), ultraviolet absorption and fluorescence-detection (SEC-DOC, SEC-UV254 and SEC-Fl254/450). Changes in pH values affected the adsorption of NOM onto TiO2, but did not affect the photodegradation sequence of NOM. For high or low pH values, the degradation of the NOM preferentially removed the larger molecular size fraction in comparison to the middle and small molecular size fractions, resulting in the relative increase of these smaller fractions. This sequence of NOM degradation leads to the evolution of the formation potential for disinfection by-products (DBPs). Specifically, the trihalomethanes and halogenated organic compounds formation potential (THMF and AOXFP) decreased steadily.
本研究考察了 pH 值对天然有机物 (NOM) 光催化降解的影响。实验在间歇式反应器(太阳模拟紫外光源)中采用 Degussa P-25 二氧化钛 (TiO2) 进行。通过尺寸排阻色谱法(DOC)、紫外吸收和荧光检测(SEC-DOC、SEC-UV254 和 SEC-Fl254/450)对 NOM 的降解进行了跟踪。pH 值的变化影响了 NOM 在 TiO2 上的吸附,但不影响 NOM 的光降解顺序。对于较高或较低的 pH 值,NOM 的降解优先去除较大分子尺寸的部分,与中小分子尺寸部分相比,导致这些较小部分的相对增加。这种 NOM 降解顺序导致消毒副产物(DBP)形成潜力的演变。具体来说,三卤甲烷和卤代有机化合物形成潜力(THMF 和 AOXFP)稳步下降。