Photocatalytic reactions of pyrene at TiO2/water interfaces

The photocatalytic oxidation of pyrene preadsorbed on TiO2 is examined in aqueous suspension under UV irradiation. Chemical oxygen demand measurements, UV-VIS spectrophotometer, infrared spectrometer and GC-MS analytical techniques were used to monitor the formed intermediates. During the oxidation processes, the ring-open reaction, hydroxylation and ketolysis occurred to produce some intermediate products (4-oxapyrene-5-one, 1,6- or 1,8-pyrenediones, 4,5-phenanthrenedialdehyde, cyclopenta[def]phenanthrene). Some factors affecting the photodegradation rate were also studied. The results were different from other studies: The pH of the dispersion, ratio of Py/TiO2:water had little effect on the photooxidation rate of pyrene catalyzed by TiO2, while the surface coverage, addition of Fe3+ affected it greatly.     

Removal of alachlor from water by catalyzed ozonation in the presence of Fe2+, Mn2+, and humic substances

The effects of Fe(II), Mn(III) and humic substances on the catalyzed ozonation of alachlor, an endocrine disruptor were investigated. Results revealed that small amounts of Fe(II), Mn(II), and humic substances could enhance the ozonation of alachlor, but larger amounts of them would retard the oxidation. These results were successfully identified by an electron paramagnetic resonance (EPR) spectroscopy spin-trapping method that could quantify hydroxyl radicals. The production of hydroxyl radicals was obviously increased with the increasing of Fe(II) concentration, which contributed to enhance ozonation at low concentrations. But the excess Fe(II) consumed some of the radicals when it was added at a higher concentration (1.5 mg/L). However, no obvious radicals were observed when a different amount of Mn(II) was used, and the catalytic ozonation of alachlor by Mn(II) mainly followed the mechanism of "active sites created on the surface of MnO2." The radical pathway was followed when alachlor was ozonated with different concentrations of humic substances because of its radical initiating, promoting, and inhibiting effects.     

机械镀锌工艺的清洁生产

结合机械镀锌的实际生产过程 ,讨论了机械镀锌实现清洁生产的主要途径 ,并且从工艺过程、经济效益、环境效益 3个方面对机械镀锌进行了综合评价 ,结果表明 ,机械镀锌是切实可行的清洁生产技术     

Fenton试剂-生物法联合处理有机废水研究进展

本文对Fenton试剂和生物法联合处理有机废水的工艺流程、适用废水种类、废水处理机理和衡量指标进行了综述,并对Fenton试剂和生物法相结合处理有机废水研究进行了展望。     

矿化垃圾生物反应床处理NOX废气的研究

矿化垃圾(稳定化垃圾)是一种良好的生物介质,可作为生物反应床的填料处理NOX废气.实验室研究表明,稳定化垃圾反应床可有效地处理NOX气体,其硝化能力(以N计)可达0.83 g/(kg·d)(干重).NOX去除率受停留时间的影响显著,NOX去除率随着停留时间的缩短而降低.当空床停留时间为1.5 min时,NOX气体的平均去除率为76.7%;空床停留时间为15 min时,NOX气体的平均去除率为91.0%.在NOX进气负荷低于110 mmol/(m3·h)时,NOX消除能力随进气负荷的增加而线性增加.当进气流量一定时,NOX去除能力随着进气NOX浓度的增加而线性增加.     

反硝化除磷的影响特性试验

采用SBR反应器（厌氧/缺氧/好氧工艺）,分别研究了乙酸盐及硝酸盐浓度变化对反硝化除磷的影响特性.试验结果表明,当进水COD浓度＞230 mg/L时,乙酸盐浓度的变化对释磷、除磷速率等影响并不显著.在硝酸盐浓度＜30 mg/L时,硝酸盐浓度越高,缺氧段除磷速率也就越高.在C/P＞23,C/N＞5条件下,SBR系统对磷、氮去除率在90%以上.     

车内空气中挥发性有机物的研究

采用热脱附-气相色谱/质谱联用法对4辆处于静止状态下的车辆内部空气中挥发性有机物（VOCs）进行了研究,共定性检出了48种有机物,其中C6～C9之间的组分较多;并对VOCs的总浓度进行了定量,1#～4#车分别为1846、2289、1104和3146 μg/m^3;其中BTEX占VOCs总量的20%～30%;车内VOCs浓度与温度及车辆使用年限密切相关.     

利用水泥处理垃圾渗滤液生物处理出水的研究

利用水泥的表面吸附和水化反应性质处理垃圾渗滤液生物处理出水可以取得很好的效果,COD的去除率可达69.5%.处理效果与水灰比、反应时间密切相关,低水灰比和较长反应时间对COD的去除更为有利.对处理前后水样的COD和TOC分析表明,水泥对非TOC贡献的COD有很强的去除效果.     

城市生活污水处理后回用作热电厂循环冷却水的可行性研究

选用适合热电厂特点的水处理剂,利用静态试验,动态模拟试验手段,对城市生活污水回用于热电厂循环冷却水系统中的复配药剂的阻垢缓蚀性能进行了研究.通过试验表明,污水回用是可行的,为城市生活污水回用于热电厂循环冷却水系统工程提供了可靠的参数.     

Fenton试剂法处理甘氨酸废水中COD的研究

通过正交试验的方法用Fenton试剂对甘氨酸生产中的工业废水进行了试验研究,分析了各因素影响程度及各影响因子的作用机理,得出了最佳的操作条件为:H2O2:COD=1.8,[Fe2 ]=40 mmol/L,反应温度40℃,pH值为3,反应时间为80 min,最终的COD去除率为68%左右.