预磁化强化ZnO@Fe3O4活化PMS降解AO7

为了研究预磁化对ZnO@Fe_3O_4活化过一硫酸盐(PMS)去除水中酸性橙7(AO7)性能的影响,考察了预磁化强度、ZnO@Fe_3O_4投量、PMS投量及初始pH对Mag-ZnO@Fe_3O_4/PMS体系降解AO7效果的影响.结果表明,当预磁化强度由0 T逐渐增大至2 T时,催化剂去除AO7的表观速率常数由0.0463 min~(-1)逐渐增大至0.1832 min~(-1),反应速率提高倍数达到1.4～4.0倍; Mag-ZnO@Fe_3O_4和PMS投量的增加对AO7的去除率均有提升效果,在最优条件下反应20 min后AO7的去除率达92%;体系初始pH对AO7降解有显著影响, pH为6～8条件下有利于Mag-ZnO@Fe_3O_4催化PMS氧化反应的进行.通过投加不同种类的猝灭剂,证实了AO7的降解主要是各种自由基共同作用的结果.经过预磁化处理后的催化剂产生感应磁场,从而影响了反应体系中自由基的复合概率,使得污染物被自由基氧化的速率提高.     

Large-scale mercury variations in Lake Vänern (Sweden) 1974-98

Lake V?nern, the largest lake in Sweden, has been seriously contaminated with mercury during the 20th century. In the 1970's and 80's the direct load, mainly from a chlor-alkali industry in the area, of mercury was drastically reduced as a response to new legislation, from three to five tons down to between five and ten kg yr(-1). Large amounts of the disposed pollutant have accumulated in the sediments. The question posed in this work is now, is the effect of the drastic load reduction after more than two decades visible in the sediments? The question is relevant as large areas still are blacklisted for fishing, but also as a follow-up of a major remedy action. The lake also serves as a freshwater reservoir for even Sweden's second largest city. This work synthesises and compares data of mercury in the sediments from three major field programs, in 1974, 1984 and 1998. The interest is focused on both spatial heterogeneity and temporal trends. In 1974, the surface concentrations are significantly higher than in subsequent surveys. Significant differences are also found between 1984 and 1998. Significant spatial differences within the lake are found for respective year. The most contaminated area is located in the north, close to the major point source (a former chlor-alkali industry). This is also the area with the largest improvement, as a direct response to the reduction in load. Further from the outlet, the recovery is more affected by burial and transport processes out into the deeper basins.     

Exposure Assessment to Mercury Vapor in Chloralkali Industry

The aim of the study was to develop a sampling method aimed at individual sampling of mercury vapor and subsequent individualexposure assessment of the worker. Hopcalite available fromInowrocawskie Zakady Chemiczne (in Poland) was founduseful for mercury vapor sampling in active and passive individual samplers. However the sampling rate determined forpassive sampler in steady-state laboratory chamber cannot be usedunder fluctuating conditions of mercury vapor concentration andair movement typical for field measurement. In order to check comparativeness of passive and active sampling methods, sampleswere taken in the same time and individual samplers fixed toworker's clothes were used. Mercury vapor concentration wasmeasured at two chloralkali industries in Poland and the resultswere presented. Excessive exposure in both industries wasconfirmed by finding elevated mercury concentration in urinesamples from the workers.     

MERCURY EMISSION INVENTORY IN ONTARIO

Mercury is released to the environment from various anthropogenic and natural sources. This work is a compilation of mercury emissions from anthropogenic sources in Ontario, Canada. The goal of our study was to identify all sources of mercury, and develop an emission inventory of anthropogenic mercury in Ontario. The result of our investigation revealed that combustion of fossil fuels and emissions from landfill sites are two primary sources of mercury to the atmosphere. Other sources of significance are emissions from waste incinerators, various industrial activities, and cement production. Total mercury emission in Ontario is estimated as 4100 kg per year.     

Preparation of rare-earth metal complex oxide catalysts for catalytic wet air oxidation

Catalytic wet air oxidation (CWAO) is one of the most promising technologies for pollution abatement. Developing catalysts with high activity and stability is crucial for the application of the CWAO process. The Mn/Ce complex oxide catalysts for CWAO of high concentration phenol-containing wastewater were prepared by coprecipitation. The catalyst preparation conditions were optimized by using an orthogonal layout method and single-factor experimental analysis. The Mn/Ce serial catalysts were characterized by Brunauer-Emmett-Teller (BET) analysis and the metal cation leaching was measured by inductively coupled plasma torch-atomic emission spectrometry (ICP-AES). The results show that the catalysts have high catalytic activities even at a low temperature (80°C) and low oxygen partial pressure (0.5 MPa) in a batch reactor. The metallic ion leaching is comparatively low (Mn<6.577 mg/L and Ce<0.6910 mg/L, respectively) in the CWAO process. The phenol, COD_Cr, and TOC removal efficiencies in the solution exceed 98.5% using the optimal catalyst (named CSP). The new catalyst would have a promising application in CWAO treatment of high concentration organic wastewater. Translated from Techniques and Equipment for Environmental Pollution Control, 2005, 6(2): 40–44 [译自: 环境污染治理技术与设备]     

Status of mercury pollution during resources development in Guizhou Province, China

1　ＩｎｔｒｏｄｕｃｔｉｏｎＧｕｉｚｈｏｕＰｒｏｖｉｎｃｅｉｓｌｏｃａｔｅｄｉｎｓｏｕｔｈｗｅｓｔＣｈｉｎａｗｉｔｈａｔｏｔａｌａｒｅａｏｆ 176.2 8ｔｈｏｕｓａｎｄｓｑｕａｒｅｋｉｌｏｍｅｔｅｒｓ,ｏｆｗｈｉｃｈ 87%ｉｓｍｏｕｎｔａｉｎ ,10 %ｉｓｈｉｌｌｓ,3%ｉｓｒｉｖｅｒ,ｂａｓｉｎａｎｄｐｌａｉｎ .Ｇｕｉｚｈｏｕｉｓａｍｏｕｎｔａｉｎｏｕｓｐｒｏｖｉｎｃｅｗｉｔｈｒｉｃｈｍｉｎｅｒａｌｒｅｓｏｕｒｃｅｓ,ａｍｏｎｇｗｈｉｃｈｍｅｒｃｕｒｙｒｅｓｅｒｖｅｒａｎｋｓｆｉｒｓｔｉｎＣｈｉｎａ,ｅｖｅｎｉ…     

废醋酸锌催化剂回收醋酸锌工艺研究

对从废醋酸锌催化剂中浸取醋酸锌进行了实验研究,考察了废催化剂颗粒大小,浸取剂种类和用量、温度和浸取时间等因素对醋酸锌浸取率的影响。     

车用催化转化器及其对发动机性能影响的研究

本文论述了影响催化转化器性能的主要因素有催化剂，催化剂的中毒失效，催化转化器的结构和排气系统的影响，温度、发动机工作状况等；强调催化转化器的结构与发动机及排气系统匹配的重要性。     

镉、汞、铅在体内对氨基酸掺入微粒体的特异性抑制作用

本实验采用DL-(~3H)-亮氨酸作为蛋白质合成的原料,从亚细胞水平观察镉、汞、铅在动物体内对肝脏各亚细胞组分蛋白合成的影响。实验结果表明,给雄性大鼠腹腔一次注入2.4mg/kg醋酸镉后72h和一次注给2.0mg/kg氯化汞或100mg/kg醋酸铅后24h,均可不同程度地抑制DL-(~3H)-亮氨酸掺入微粒体蛋白,而对其它组分包括细胞核、线粒体、去微粒体后上清液蛋白中DL-(~3H)-亮氨酸的掺入无明显影响。     

治理催化超临界水氧化处理1,5-萘二磺酸

采用Mn2O3γAl2O3和V2O5γAl2O3为催化剂,在一连续流固定床反应器中进行了超临界水氧化1,5萘二磺酸实验。实验结果表明,在380～440℃,24MPa条件下,Mn2O3γAl2O3和V2O5γAl2O3催化剂对1,5萘二磺酸的氧化降解具有显著的促进作用,TOC去除率达到90%以上;催化剂的催化效果随反应温度的升高而增强,随pH值的降低而增强,随停留时间的延长先增强后趋于平缓。