不同加热方式下催化氧化甲苯的性能研究

研究考察了微波单模腔、多模腔与传统电炉三种不同加热方式下甲苯的催化氧化性能,分析不同加热方式下进出口气体温度和固定床反应温度的变化,并对实验前后的Cu-Mn-Ce/TiO2-分子筛催化剂进行了扫描电镜、X射线衍射和比表面积等表征测试.研究表明,相同工艺条件下电炉加热、微波多模腔与单模腔加热对甲苯的去除效率分别为77%、83%和94%,对应的床层反应温度为265℃、215℃和145℃,微波加热的选择性、"热点效应"和偶极极化作用提高了甲苯的降解效率并降低其氧化温度和工艺处理能耗,微波单模腔内高的能量密度显著提高了甲苯的氧化效率并降低反应温度.催化剂表征发现,微波加热对催化剂结构与活性组分的分布几乎没有影响,而电炉加热则导致催化剂表面烧结与活性组分团聚,微波加热下催化剂更大的比表面积有利于甲苯的吸附与氧化降解.     

大气颗粒物吸湿性研究

大气颗粒物吸湿性是反映颗粒物理化性质的重要指标,吸湿性研究对深入了解颗粒物的环境和健康效应具有重要意义. 总结了国外近年来大气颗粒物吸湿性研究进展:①典型的大气颗粒物吸湿性分析方法为H-TDMA(吸湿性串联差分电迁移率粒径分析仪)系统及其优化方法. ②大气颗粒物吸湿性呈单峰、双峰甚至多峰分布;根据G_f(吸湿性生长因子)随粒径变化的模式,可将大气颗粒物分为强吸湿性和弱吸湿性2类,也可分为纯不溶性、混合不溶性、混合可溶性和纯可溶性4类. ③城市背景点颗粒物的G_f比城市观测点高;城市观测点的颗粒物G_f分布呈夏季高、冬季低,白天高、晚上低的特征. ④颗粒物吸湿性与其化学组成和形态密切相关,纯可溶性盐颗粒物的G_f通常较高. ⑤柴油燃烧源新排放的颗粒物属于弱吸湿性颗粒物,G_f非常小,但在其表面老化后或随燃料中硫含量的增加G_f会明显变大. ⑥生物质燃烧排放颗粒物的G_f相对较高,但存在区域差异性. 针对国内大气颗粒物吸湿性研究现状,提出了未来重点研究方向.      

The Precautionary Principle and the Prevention of Marine Pollution

This paper argues that the environmental changes witnessed in the past decade call for a new approach to environmental management; an approach based not on the principle of the assimilative capacity of the environment but on the precautionary principle, and the emerging preventive environmental paradigm. Uncertainties in scientific knowledge and complexities in ecological systems have presented specific failures of the assimilative capacity methodology. It is argued that these failures are not circumstantial in nature, nor are they the result of misapplication of science by scientists. Rather, they represent inherent problems in the use of the assimilative capacity concept in environmental management. The emergence of the precautionary principle is discussed and a formulation of the principle is presented. In conjunction with the operational approach of clean production, we believe that this principle offers a sounder basis for the prevention of marine pollution in the next decade.     

Spatial distribution of copper in relation to recreational boating in a California shallow-water basin

The overall effect of the number of boats on the copper (Cu) levels in the water column and sediment, along with their spatial variability within Shelter Island Yacht Basin (SIYB), San Diego Bay, California was examined. We identified a horizontal gradient of increasing dissolved Cu and Cu in sediment from outside to the head of SIYB which was coincident with the increasing number of boats. Spatial models of Cu distribution in water and sediment indicated the presence of ‘hotspots’ of Cu concentration. From outside to the head of SIYB, dissolved Cu ranged from 1.3 μ g L^?1 to 14.6 μ g L^?1 in surface water, and 2.0 μ g L^?1 to 10.2 μ g L^?1 in bottom water. Cu in sediment exceeded the Effect Range Low of 34 mg kg^?1 (i.e. where adverse effects to fauna may occur), with a peak concentration of 442 mg kg^?1 at the head of the basin. Free Cu⁺⁺ in surface water was several orders of magnitude higher than in sediment porewater. High-resolution data of Cu species together with probability maps presented in this paper will allow managers to easily visualise and localise areas of impaired quality and to prioritise which areas should be targeted to improve Cu-related conditions.     

Assessment of regional ecological security based on ecological footprint and influential factors analysis: a case study of Chongqing Municipality,China

In recent years, it has been important to objectively evaluate the degree of regional ecological security with regard to resource depletion and to analyse influential factors to assess sustainable development. This paper tries to assess ecological security in Chongqing while investigating the main influencing factors. Calculations of the consumption footprint, production footprint and ecological capacity for Chongqing from 1996 to 2007 based on an ecological footprint approach were carried out. An ecological security index was also calculated from these results and factors influencing security were analysed using factor analysis. Both the consumption and production footprints present an upward trend, contrary to the gradually decreasing trend of ecological capacity. In addition, the ecological security index shows that Chongqing has deteriorated from a level of less risk to that of risk. Factor analysis suggests that the deterioration of ecological security could primarily be ascribed to socio-economic factors and industrialisation. With socio-economic development and industrialisation, appropriate measures must be taken to improve the ecosystem in Chongqing so as to achieve sustainable development. The limitations of the methodology are also discussed and areas that require further research are presented.     

中部6省生态足迹的测算与比较分析

生态足迹方法是区域可持续发展研究的一种重要方法,在中部6省大区域框架下,运用生态足迹模型对中部6省1989—2011年的生态足迹进行了测算和对比研究。研究结果表明:中部6省1989—2011年的生态承载力较为平稳,其中江西、河南、湖北和湖南4省的生态承载力略有上升,而山西、安徽两省的生态承载力有下降趋势。中部6省的社会经济活动对生态系统的消耗远大于生态系统本身的承载能力,并且这种差距正在不断增大,导致生态赤字不断增大。考察期间,山西省生态赤字的绝对值最小,平均生态赤字为0.49 hm2 cap-1,湖北省生态赤字最大,平均值为1.15 hm2 cap-1,其次为河南和湖南,生态赤字增长最快的是山西省和河南省,增长倍数分别达到了7.38和4.27倍。中部6省6种生态生产性土地的生态足迹均呈现出上升趋势,平均来看,6类生态生产性土地在中部6省总的生态足迹中所占比重由高到低依次为耕地、化石能源地、草地、建筑用地、水域、林地。耕地生态足迹是生态足迹中最重要的组成部分,在总的生态足迹中所占比重最大,中部6省耕地的生态足迹时间序列数据比较平稳,在考察时间内从1989年的0.4241上涨到2011年的0.5851,上升趋势较平稳,但由于耕地生态足迹所占比重大,尽管增长速度缓慢,但对中部6省生态足迹总的影响较大。建筑用地和林地生态足迹虽然增长幅度较大,但由于基数小,因此建筑生态足迹和林地生态足迹对中部6省生态足迹总的影响较小。草地、水域和化石能源用地生态足迹基数大,增长幅度也大,加上耕地生态足迹,共同决定了中部6省人均生态足迹的逐年上升趋势。     

大气环境影响评价现状空气质量监测布点技术方法

基于HJ2.2—2008《环境影响评价技术导则-大气环境》的规定,结合某石化焦化扩建案例实践,对大气环境影响评价现状空气质量监测方案的制定、监测布点原则与技术要点进行了深入系统地研究,进一步探讨了在环评中执行的具体问题及解决方案。     

响应面法在催化湿式氧化降解异佛尔酮中的应用

以Ru/TiZrO2为催化剂,采用催化湿式氧化法降解异佛尔酮废水,选择反应温度、氧气分压、反应时间、催化剂用量、初始pH为影响因素,以TOC去除率为响应值,采用响应面法研究影响因素及其交互作用对响应值的影响,建立二次多项式回归方程模型,并采用后退回归法进行模型精简.结果表明,反应时间和反应温度及其交互作用对TOC去除率影响极显著(P≤0.01);反应时间的二次项对TOC去除率影响显著(P≤0.05).随着反应温度的升高和反应时间的延长,TOC去除率逐渐提高.最后对模型进行验证,实验值与预测值具有很好的一致性,说明模型具有可靠的预测性,将该模型应用到催化湿式氧化中合理可行.质谱和离子色谱检测到异佛尔酮的降解产物主要为有机酮与小分子羧酸,由此提出对反应机理和降解途径的假设.     

基于宏基因组技术获得的对厌氧氨氧化菌代谢的新理解

厌氧氨氧化菌(Anaerobic ammonium oxidation bacteria,AAOB)是化能自养菌,由于其生理代谢的奇异性、细胞结构的特殊性以及对氮素循环的重要性,已成为环境工程、微生物以及海洋生物学等领域的研究热点.然而,AAOB未能实现纯培养的现状已成为AAOB代谢途径研究的巨大障碍.近年来兴起的宏基因组技术(Metagenomics)为AAOB代谢途径的研究提供了新手段.采用宏基因组技术,可直接研究微生物群体中某特定微生物基因组的结构与功能,摆脱了传统微生物学研究对纯培养的依赖,使未培养微生物的认识和开发成为可能.本文首先简述获取AAOB宏基因组信息的过程,然后通过比较由传统代谢研究方法和宏基因组技术获得的AAOB代谢途径的研究成果,论述基于宏基因组技术获得的对AAOB代谢的新理解,得出以下结果和结论:1)AAOB的碳素固定途径为乙酰辅酶A途径,碳素固定的还原力来自NADH或者QH2;2)AAOB氮素转化的重要中间产物是NO,而非NH2OH,并提出了以NO为核心的AAOB代谢的改进模型;3)AAOB的ATP合成途径为氧化磷酸化,推测的电子传递途径为N2H4—QH2—细胞色素bc1复合体;细胞色素bc1复合体再将电子用于NO2-还原和N2H4合成.AAOB的宏基因组技术使AAOB代谢途径的研究更具方向性.随着分子生物学理论和技术的不断发展,宏基因组学的升级技术(如宏转录组学、宏蛋白质组学)将为AAOB代谢途径的研究提供新的方法与平台.图3表1参51     

Reduction of hexavalent chromium with scrap iron in a fixed bed reactor

The reduction of hexavalent chromium by scrap iron was investigated in continuous long-term fixed bed system. The effects of pH, empty bed contact time (EBCT), and initial Cr(VI) concentration on Cr(VI) reduction were studied. The results showed that the pH, EBCT, and initial Cr(VI) concentration significantly affected the reduction capacity of scrap iron. The reduction capacity of scrap iron were 4.56, 1.51, and 0.57 mg Cr(VI)·g^-1 Fe⁰ at pH 3, 5, and 7 (initial Cr(VI) concentration 4 mg·L^-1, EBCT 2 min, and temperature 25°C), 0.51, 1.51, and 2.85 mg Cr(VI)·g^-1 Fe⁰ at EBCTs of 0.5, 2.0, and 6.0 min (initial Cr(VI) concentration 4 mg·L^-1, pH 5, and temperature 25°C), and 2.99, 1.51, and 1.01 mg Cr(VI)·g^-1 Fe⁰ at influent concentrations of 1, 4, and 8 mg·L^-1 (EBCT 2 min, pH 5, and temperature 25°C), respectively. Fe(total) concentration in the column effluent continuously decreased in time, due to a decrease in time of the iron corrosion rate. The fixed bed reactor can be readily used for the treatment of drinking water containing low amounts of Cr(VI) ions, although the hardness and humic acid in water may shorten the lifetime of the reactor, the reduction capacity of scrap iron still achieved 1.98 mg Cr⁶⁺·g^-1 Fe. Scanning electron microscope equipped with energy dispersion spectrometer and X-ray diffraction were conducted to examine the surface species of the scrap iron before and after its use. In addition to iron oxides and hydroxide species, iron-chromium complex was also observed on the reacted scrap iron.