College of Science, Huazhong Agricultural University, Wuhan 430070, PR China.
Environ Technol. 2011 Oct;32(13-14):1515-22. doi: 10.1080/09593330.2010.543927.
The photocatalytic degradation of a commercial methyl parathion (MP) under UV irradiation was investigated in aqueous suspension containing lanthanum-doped mesoporous TiO2 nanoparticles (La/m-TiO2) as photocatalyst. The rate of photodecomposition of MP was measured using UV-Vis spectrophotometry, and its mineralization was followed using ion chromatography (IC). The identification of possible intermediate products was carried out using several powerful analytical techniques such as gas chromatography-pulsed flame photometric detector (GC-PFPD) and high performance liquid chromatography-mass spectroscopy (HPLC-MS). Under our conditions, complete disappearance of 20 mg/L of MP occurred within 2 h of illumination, whereas complete mineralization of MP was not achieved through IC analysis. There was a single intermediate product found in the research, which was identified to be methyl paraoxon, owing to the substitution of S by the O atom in the MP molecule. Based on the experimental facts, it is concluded that MP was mainly attacked not by OH radicals but photo-generated holes (h+), resulting from the good adsorption of MP on the catalyst surfaces due to the enhanced adsorption by La doping.
在含有镧掺杂介孔 TiO2 纳米粒子(La/m-TiO2)的水悬浮液中,研究了在紫外光照射下商业甲基对硫磷(MP)的光催化降解。使用紫外可见分光光度法测量 MP 的光分解速率,并使用离子色谱(IC)跟踪其矿化。使用几种强大的分析技术,如气相色谱-脉冲火焰光度检测器(GC-PFPD)和高效液相色谱-质谱联用(HPLC-MS),对可能的中间产物进行了鉴定。在我们的条件下,20mg/L 的 MP 在光照 2 小时内完全消失,而通过 IC 分析并未实现 MP 的完全矿化。研究中发现了一种单一的中间产物,由于 MP 分子中 S 原子被 O 原子取代,因此被鉴定为甲基对氧磷。根据实验事实,可以得出结论,MP 主要不是被 OH 自由基攻击,而是被光生空穴(h+)攻击,这是由于 MP 由于 La 掺杂而增强了对催化剂表面的吸附,从而在催化剂表面上得到了很好的吸附。