固相微萃取法在环境监测中应用

对固相微萃取法（ＳＰＭＥ）在环境监测中应用予以综述，列表比较了一些有机化合物的研究情况，并指出了ＳＰＭＥ法的发展趋势     

金属和有机化合物污水的处理TiO2光催化剂的研究

本文通过试验室试验，研究了利用ＴｉＯ２光催化剂处理带有溶解金属（Ａｇ，Ａｕ，Ｃｄ，Ｃｒ，Ｃｕ，Ｈｇ，Ｎｉ和Ｐｔ）及各种有机物（如：甲醇，甲酸，水扬酸，乙二胺四乙酸，酚，硝基苯）的污水，研究发现只要具有一半反应标准的还原电势，正高压高于３Ｖ的金属（做为正常氢电极的函数）可以和ＴｉＯ２做为催化剂进行处理。同时本文还提供了说明氧化和还原反应之间相互作用的动力学数据，试验利用单苯环同系物做为电子供体，说明     

挥发性有机化合物装卸作业中蒸气回收处理技术与管理

在提出防治挥发性有机化合物蒸气污染重要性的基础上，分析了中国港口挥发性有机化合物蒸气污染，防治及管理现状，并进一步对MARPOL73／78附则Ⅵ一防止船舶大气污染规则中有关控制挥发性有机化合物释放有毒蒸气造成港口大气污染的问题进行了讨论。     

Catalytic dechlorination of chlorobenzene in water by Pd/Fe bimetallic system

IntroductionChlorinatedorganiccompoundshavebeenusedonalargescaleinthechemical,petrochemical,andelectronicindustries.Inrecentyears ,worldwideattentionhasbeengiventotheenvironmentalandhealthimpactofthemasaclassofcontaminants .Severalareknowntocauseozonedepletion ,whileothersproduceadverseeffectsonthehumancentralnervoussystemandhavebeenlinkedtodiseasessuchascancer.Almostallofthechlorinatedaromaticcompoundsaretoxicandthermallystable .Oncereleasedintoenvironment,theywillaccumulateinthesurroundings…     

一种新的拓扑指数及其在有机化合物结构/性质相关性研究中的应用

以距离矩阵为基础，提出一种表征化合物分子结构的拓扑指数，并将其用于预报饱和链烃类、醇类和含氮芳香类化合物的性质和活性，获得了满意的结果。     

藻类生态毒理学研究进展

综述了重金属和部分有机化合物对藻类的生态毒理效应,并探讨了藻类对污染物的富集和降解机制.大量研究证实,重金属对藻类在各个水平上均产生影响,但不同重金属对不同的藻种有不同的毒性效应.而有机物对藻类的影响则可归纳为4个方面.     

生物净化挥发性有机化合物(VOCs)的研究进展

有机废气中大多含有低浓度的苯、甲苯、苯乙烯、多环芳烃等挥发性有机化合物(VOCs)。这类挥发性有机化合物会对人体健康和生态环境造成危害。治理VOCs污染是大气污染治理的重要部分。生物法处理有机废气具有运行费用低、没有二次污染等优点。常用的生物处理技术主要有生物过滤池、生物滴滤池和生物洗涤塔。20世纪80年代生物法在欧洲得到快速发展,我国于90年代以后也开始了生物处理VOCs废气的研究,并取得了一定的成就。     

城市水循环中的微量污染物负荷

污水中不同的有机化合物,例如,药物、个人护理产品中的添加物、家用化学物质和工业化学等物质都对水生生态系统和人类健康带来了潜在威胁.这些污染物质的大部分在环境中含量非常低,范围在pg/L至ng/L间,因此,被称为微量污染物.这些微量污染物质对水生生态系统和人类健康的威胁表现在内分泌干扰作用、化学敏感作用,污染混合物的交互作用以及长期暴露下的慢性作用.     

Reversibly enhanced aqueous solubilization of volatile organic compounds using a redox-reversible surfactant

Surfactant-enhanced remediation (SER) is an effective method for the removal of volatile organic compounds (VOCs) from contaminated soils and groundwater. To reuse the surfactant the VOCs must be separated from the surfactant solutions. The water solubility of VOCs can be enhanced using reversible surfactants with a redox-acive group, (ferrocenylmethyl)dodecyldimethylammonium bromide (Fcl2) and (ferrocenylmethyl)tetradecanedimethylammonium bromide (Fcl4), above and below their critical micelle concentrations (CMC) under reducing (I⁺) and oxidative (I²⁺) conditions. The CMC values of Fcl2 and Fcl4 in I⁺ are 0.94 and 0.56 mmol/L and the solubilization of toluene by Fcl2 and Fcl4 in I⁺ for toluene is higher than the solubilization achieved with sodium dodecyl sulfate, cetyltrimethylammonium bromide and Trition X-114. The solubilization capacity of the ferrocenyl surfactants for each tested VOCs ranked as follows: ethylbenzene > toluene > benzene. The solubilities of VOCs by reversible surfactant in I⁺ were 30% higher than those in I²⁺ at comparable surfactant concentrations. The effects of Fcl4 concentrations on VOCs removal efficiency were as follows: benzene > toluene > ethylbenzene. However, an improved removal efficiency was achieved at low ferrocenyl surfactant concentrations. Furthermore, the reversible surfactant could be recycled through chemical approaches to remove organic pollutants, which could significantly reduce the operating costs of SER technology.     

Effects of metal and acidic sites on the reaction by-products of butyl acetate oxidation over palladium-based catalysts

Catalytic oxidation is widely used in pollution control technology to remove volatile organic compounds. In this study, Pd/ZSM-5 catalysts with different Pd contents and acidic sites were prepared via the impregnation method. All the catalysts were characterized by means of N2 adsorption- desorption, X-ray fluorescence （XRF）, HE temperature programmed reduction （H2-TPR）, and NH3 temperature programmed desorption （NH3-TPD）. Their catalytic performance was investigated in the oxidation of butyl acetate experiments. The by-products of the reaction were collected in thermal desorption tubes and identified by gas chromatography/mass spectrometry. It was found that the increase of Pd content slightly changed the catalytic activity of butyl acetate oxidation according to the yield of CO2 achieved at 90%, but decreased the cracking by-products, whereas the enhancement of strong acidity over Pd-based catalysts enriched the by-product species. The butyl acetate oxidation process involves a series of reaction steps including protolysis, dehydrogenation, dehydration, cracking, and isomerization. Generally, butyl acetate was cracked to acetic acid and 2- methylpropene and the latter was an intermediate of the other by-products, and the oxidation routes of typical by-products were proposed. Trace amounts of 3-methylpentane, hexane, 2-methylpentane, pentane, and 2-methylbutane originated from iso4merization and protolysis reactions.