Carbon nanotubes-incorporated MIL-88B-Fe as highly efficient Fenton-like catalyst for degradation of organic pollutants

CNTs were incorporated into MIL-88B-Fe to get a new Fenton-like catalyst (C@M). Fe(II) was introduced in C@M to get a fast initiation of Fenton-like reaction. Fe(II) content in C@M was related with oxygen-containing functional groups on CNTs. C@M shows efficient catalytic degradation of pollutants over a wide pH range. Iron-based metal organic frameworks have been verified to be efficient heterogeneous Fenton catalysts due to their open pore channels and highly uniform distribution of metallic centers. In these catalysts, however, the iron element is mainly in the form of Fe(III), which results in a process required to reduce Fe(III) to Fe(II) to initiate Fenton reaction. To address this problem, carbon nanotubes (CNTs) with electron-rich oxygen-functional groups on the surface were incorporated into the metal organic frameworks (MIL-88B-Fe) to improve Fe(II) content for an enhanced Fenton-like performance. The prepared CNT@MIL-88B-Fe (C@M) showed much stronger catalytic ability toward H₂O₂ than MIL-88B-Fe. The pseudo-first-order kinetic constant for phenol degradation by C@M (0.32 min^–1) was about 7 times that of MIL-88B-Fe, and even higher than or comparable to the values of reported heterogeneous Fenton-like catalysts. Moreover, the Fenton-like system could effectively degrade various kinds of refractory organic pollutants and exhibited excellent catalytic activity over a wide pH range (4–9). XPS analysis confirmed that Fe(II) content of the catalyst gradually increased with CNT loadings. Electron spin resonance analysis showed that the signal intensity (•OH) of C@M was much higher than MIL-88B-Fe, which was consistent with the degradation efficiency of pollutants. Furthermore, the Fe(II) content of the catalyst gradually increased along with the oxygen-functional group content of CNTs. The result demonstrated that oxygen-containing functional groups of CNTs have a significant impact on the enhanced catalytic performance of C@M. This study provides a new insight to enhance Fenton reaction by using nanocarbon materials.     

乙醇汽油对减少机动车污染排放的机理研究与分析

以93#国Ⅲ乙醇汽油(E10)、93#国Ⅲ普通汽油和93#国Ⅳ普通汽油为实验对象,对GB18352.3-2005中要求限定的CO、HC和NOx,以及颗粒物(PM)和CO2等主要污染物的排放进行了测量和对比研究,并对CO、HC、PM、NOx、CO2和苯系物等污染物的形成原因和减排机理进行了分析.和93#国Ⅲ普通汽油相比,93 #国Ⅲ乙醇汽油(E10)排放的尾气中:CO降低了19.7％,HC降低了16.4％;和93#国Ⅳ普通汽油相比,93#国Ⅲ乙醇汽油(E10)排放的尾气中:CO降低了1.8％,HC降低了12.9％,CO2降低了2.4％.研究表明,乙醇汽油在减少CO、HC、NOx、颗粒物和苯系物等有毒物质排放方面具有显著功效,使用乙醇汽油可以减少环境污染物的排放,显著改善空气质量.     

藻类与有机污染物间的相互作用研究

本文就若干有机污染物对藻类的毒性效应及藻类对这些污染物的富集降解作用进行了系列研究。结果表明，不同污染物对藻类的毒性有很大差别，其中三有机锡的毒性最大。此外，不同藻类对毒物具有不同的敏感性，其中扁藻Platymonas sp.和斜生栅藻S．obliquus最敏感。藻类通过生物富集和生物降解两种途径去除水中污染物，其中，邻苯二甲酸二丁酯最容易被去除。藻类固定化能够在一定程度上增加藻类对污染物的降解。     

大气污染指示植物的研究

自50年代以来.为寻找一种经济、实用和灵敏的方法来监测环境变化,开展了大量大气污染指示植物的研究.这些工作包括用植物叶片典型症状、树皮、草本植物、附生植物指示气体污染(O_3、PANs、NO_x、SO_2、HF、乙烯等)、粉尘以及重金属污染.进入80年代以后,有关研究集中到利用植物富集的污染物含量结合计算机等先进技术指示和监测大气环境变化及进行大气质量评价.本文对国内外开展的大气污染指示植物研究的历史及其主要方法作了简要介绍,并就利用植物指示和监测大气污染的若干问题进行了探讨.     

复合人工湿地对有机污染物的去除效果初步研究

研究了由不同植物配置(驯化和未驯化)的两组下行和上行植物床组成的复合人工湿地对生活污水的净化效果。结果表明,CODCr和BOD5的去除率达67.3%,68.1%,总氮(TN)的去除率为26.9%,总磷(TP)的去除主要发生在上行床,去除率为81.6%。环芳烃(PAHs)中苊(Ace)、荧蒽(Flu)、芘(Py)、苯并[a]蒽(BaA)、屈(Chr)、苯并[b]荧蒽(BbF)、苯并[a]芘(BaP)、茚并[1,2,3-cd]芘(InP)和苯并[g,h,i](BPR)经下行床后,去除率超过80%,上行床去除较少。驯化床和未驯化床对PAHs的去除效果差异不显著。邻苯二甲酸酯(PAEs)中邻苯二甲酸二乙酯(DEP)和邻苯二甲酸二异丁酯(DiBP)经驯化床后,质量浓度显著升高,经未驯化床后邻苯二甲酸二(2-乙基)己酯(DEHP)含量显著降低。蚕豆根尖微核实验表明,不同植物配置对微核率影响差异并不显著,毒害物质经下行床后大部分被去除。     

用黑麦幼苗法测定土壤中污染元素的生物有效性

本文对全国污灌区１２个土样中Ｃｄ形态与生物有效性的试验表明，Ｃｄ的交换态，吸附态，有机结合态均有效，且有机结合态最为有效，对紫阳县富硒土壤的试验表明：黑麦幼苗中的总Ｓｅ量与０．１ｍｏｌ／１ＫＨ２ＰＯ４的浸提量最为相关，从而推荐该法为酸性土壤有效Ｓｅ的浸提方法，对西安污水厂污水污泥在娄土上不同施用量的试验表明：幼苗中Ｎ，Ｐ随施用量增加而增加，Ｎ，Ｐ的有效率分别为５０－７０％及１５－２８％；黑麦幼苗中     

Geochemical evidence of pollutants from coalfired generating stations in late Pleistocene palaeosols in the Dalijia Shan,northwestern China

Surface palaeosols in two tills and a diamicton from an area in northwestern China were analysed for geochemical pollutants. Elevated levels of Br, As and Sb indicate that pollution from coal-burning and/or coal-fired electricity generating stations is delivered by aeolian transport into palaeosols dating from the last glaciation. Because the climate in the field area is sub-humid (precipitation <760 mm) the relative movement of soluble elements in palaeosols dating from early and late stades of the last glaciation is not expected to be high. The glacial and aeolian parent materials of the palaeosols indicate differences that are probably related to their source areas and to the incorporation of geochemical pollutants.     

分子连接性指数对部分有机污染物溶解度及疏水参数的预测

以化学键为基础定义了键连接性指数和分子键连接性指数，分子键连接性指数与卤代烷、环烷烃、烷基苯和含氧原子醇、酮、醚及卤代苯等有机污染物的溶解度和辛醇／水分配系数都具有良好的线性关系，使用该模型对化合物的溶解度及疏水参数的估算结果接近实验值，能很好地反映有机化合物的结构特性，可应用于不饱和碳氢体系和各类杂原子体系，且具有良好的预测能力。     

Metals and organic pollutants in snow surrounding an iron factory

To estimate air pollution snow samples were collected in March 2001 at six sites in the vicinity of the Kostomuksha factory in Karelia. Seventy-two chemical elements and more than 200 individual organic compounds were identified by inductively coupled plasma mass spectrometry (ICP-MS) and gas chromatography mass spectrometry (GC-MS). It was found that the levels of Li, B, Al, Fe, Ni, Cu, Zn, Hg, Mn, Mo as well as hydrocarbons, phthalates and phenols exceeded the existing maximum allowable concentrations. A list of toxicants emitted with the factory exhausts and a list of priority pollutants for Kostomuksha were compiled. The impact of the exhausts of the Kostomuksha factory on the environment in Finland is relatively small. Electronic Publication     

Monitoring of waste deposit derived groundwater contamination with organic tracers

Specific anthropogenic substances derived from seepage and leakage water from a waste deposit landfill were analysed in groundwater and drainage effluents using gas chromatography-mass spectrometry (GC/MS). Here, we demonstrate the application of an organic marker approach to study lateral and vertical distribution of contamination as well as the long-term emission behaviour. Source-specific and environmentally-stable pesticides, plasticisers and pharmaceuticals, such as N,N-diethyl toluamide, N-butyl benzene sulfonamide, clofibric acid, mecoprop and bisphenol A, were quantitatively analysed. A distinct lateral expansion was detected. Although temporal variations were high, no significant trend was observed.