扩散法测定环境空气中的二氧化硫

介绍了利用自制分子扩散式个体采样器 ,监测环境空气中的二氧化硫的方法 ,该方法改 PRA光度法为离子色谱法 ,提高了方法的灵敏度。经实验室性能评价能够满足实验室测试的要求。并经有动力的溶液吸收管法现场对比测试 ,两种测试方法结果一致     

Ag/Al2O3催化剂用于碳氢化合物选择性还原NO

比较了富氧条件下CH4、C3H8、C3H6和C2H5OH分别用作还原剂时,NO在Ag/Al2O3催化剂上的还原活性.结果表明, CH4和C3H8还原NO的活性很低,而C3H6和C2H5OH能有效地还原NO.在此基础上,研究了H2O和SO2对C3H6和C2H5OH在Ag/Al2O3催化剂上还原NO活性的影响.结果表明,H2O的存在会降低低温区的NO还原活性,而且这种影响是可逆的.将H2O 和SO2同时加入反应混合气,引起NO还原活性较大幅度降低,结合程序升温脱附实验结果,认为可能是由于存在SO2时,Ag/Al2O3催化剂吸附NO的能力降低.     

SO2污染对小鼠骨髓细胞微核的诱发作用

在SO2吸入慢性染毒条件下,小鼠骨髓嗜多染红细胞（PCE）的微核细胞率与微核率均显著增加,且雌雄差异显著。结果也表明,SO2对阳性致突变剂乌拉坦航发微核的作用有显著抑制效应。本研究模拟SO2空气污染,从整体水平直接证实了SO2是哺乳类细胞染色体断裂剂、SO2与阳性致突变剂的联合作用是复杂的结论。     

不同DSA类阳极催化降解苯胺的试验研究

很多工业都产生苯胺废水。本文用新兴的电化学催化系统 ,采用特殊工艺自制的两种 DSA类电极作为阳极 ,对自配的苯胺溶液进行了降解处理 ,并得出了本试验范围内的最佳条件。     

环状扩散管-分级采样器的建立和细粒子酸性的测定

建立了国内第一台扩散管－分级采样器，用来研究大气气胶溶胶的组成和细粒子的酸性，实验证明该采样系统能够有效地避免大气中的碱性物质对颗粒物采样的干扰。在北京，湖南等地进行了现场实验，测定了气溶胶的酸性。     

On the influence of sand-wind on atmospheric environment

The authors seek, through tests on simulated sand samples in a wind tunnel and analysis of minerals combination and trace elements, to discover the environmental implications of flying-up, falling-down and concentration variation as a function of natural wind speed and direction, distance of movement, range and extent of influence on the atmospheric environment, of micro-granular components on the ground surface in the Keerqin desert area in northwest Liaoning Province of China.     

Experimental and theoretical studies on NO selective catalytic oxidation over α-MnO2

Based on the experimental and theoretical methods, the NO selective catalytic oxidation process was proposed. The experimental results indicated that lattice oxygen was the active site for NO oxide over the $\mathrm{\alpha }$-MnO₂(110) surface. In the theoretical study, DFT (density functional theory) and periodic slab modeling were performed on an $\mathrm{\alpha }$-MnO₂(110) surface, and two possible NO oxidation mechanisms over the surface were proposed. The non-defect $\mathrm{\alpha }$-MnO₂(110) surface showed the highest stability, and the surface O_s (the second layer oxygen atoms) position was the most active and stable site. O₂ molecule enhanced the joint adsorption process of two NO molecules. The reaction process, including O₂ dissociation and O=N-O-O-N=O formation, was calculated to carry out the NO catalytic oxidation mechanism over $\mathrm{\alpha }$-MnO₂(110). The results showed that NO oxidation over the $\mathrm{\alpha }$-MnO₂(110) surface exhibited the greatest possibility following the route of O=N-O-O-N=O formation. Meanwhile, the formation of O=N-O-O-N=O was the rate-determining step.     

2-Chlorophenol oxidation kinetic by photo-assisted Fenton process

Experimental data are presented to test and validate a kinetic model for the oxidation of 2-chlorophenol wastewater by photo-assisted Fenton process. The data showed that this process had produced good effects under acidic conductions. Up to 90% 2-chlorophenol was removed after 90-minute reaction time with H2O2 of 25% CODCr. in, while in UV/H2O2 system ordy 16.8% 2-chlorophenol was removed after one hour treatment. The optimal pH in this reaction occurred between pH 3.0 and pH 4.0. The reaction kinetics for photo-assisted Fenton process experimented in this research was investigated. Kinetic models were proposed for the treatment of 2-chlorophenol wastewater. The reaction was found to follow the 2nd order. The equations of reaction kinetics are as follows:-d[RH]/dt=KRH[RH][H2O2]0exp(-KH2o2t);-d[CODCr]/dt=KCODCr[CODCr][H2O2]0exp(-K′t).The prediction of the models was found to be in a good agreement with experimental results, thus confimfing the proposed reaction mechanism.     

Catalysts for decomposing ozone tail gas

The preparation of immobilizing-catalysts for decomposing ozone by using dipping method was studied. XRD, XPS and TEM were used to characterize the catalysts. The three kinds of catalysts were selected preferentially, and their catalytic activities were investigated. The results showed that the catalyst with activated carbon dipping acetate( active components are Mn:Cu = 3:2, active component proportion in catalyst is 15%, calcination temperature is 200℃ ) has the best catalytic activity for ozone decomposing. One gram of catalyst can decompose 17.6g ozone at initial ozone concentration of 2.5g/m^3 and the residence time in reactor of 0.1s. The experimental results also indicated that humidity of reaction system had negative effect on catalytic activity.     

磁性吸附材料CuFe2O4吸附砷的性能

根据Cu(Ⅱ)和Fe(Ⅲ)都对砷有较强的亲和性,制备了同时含有Cu(Ⅱ)和Fe(Ⅲ)的、可用磁分离方法进行分离回收的磁性吸附材料CuFe2O4,并对其进行了表征及吸附砷的性能研究.结果表明,该吸附剂对砷的吸附能力与溶液pH有关,在弱酸性及中性条件下,吸附砷的能力最强,而对As(V)的吸附能力比对As(Ⅲ)更强些,在平衡浓度为10μg/L时,其吸附容量可达10mg/g左右,可以很容易地将水中浓度为1～20mg/L的As(V)降到10μg/L以下.实验考察了几种无机阴离子对吸附砷的影响,表明较高浓度(砷浓度的20倍)的硫酸盐对As(Ⅲ)和As(V)的吸附均有一定影响,盐酸盐及磷酸盐则影响不明显;负载的As(V)可较容易地用0.1mol/L NaOH洗脱下来,使吸附剂再生,而As(Ⅲ)则难以洗脱,这与2种价态砷的吸附机理不同有关.