废铜提炼回收贵重金属加工生产中“三废”综合利用及治理

以废铜为原料冶炼贵重金属是资源综合回收利用的有效途径之一,通过对典型废铜冶炼加工企业污染因子产生及排放分析,进行综合回收利用和有效治理,旨在回收贵重金属的同时,减少二次污染,＂三废＂达标排放,在发展铜加工产业基础上实现铜资源循环利用,达到污染减排的目的。     

工业废水催化湿式氧化处理的研究

采用系列贵金属-半导体氧化物催化剂,在高压釜中250℃液相条件下对焦化厂等工业废水以及由氨、吡啶等组成的模拟废水进行液相氧化试验。结果发现几种催化剂对不同污染物有不同序列的催化氧化活性,其净化作用有各自的选择性。WT-501催化剂对氨和有机污染物均有高活性,焦化废水经WT-501催化氧化处理后’COD、NH_3分別从9302mg/L和5230mg/L降至619mg/L和47mg/L,去除率高达93.2％和99％。     

贵金属-稀土复合型催化剂的制备与性能研究

制备了净化车辆尾气的贵金属稀土复合型催化剂,对该催化剂进行了活性测试和结构表征.利用所制备的催化剂在摩托车上进行了性能研究.实验结果表明,采用催化剂后,可使车辆排放达到欧洲Ⅱ号标准,表明所研制的催化剂具有较好的应用价值.     

Simulating mesoscale transport and diffusion of radioactive noble gases using the Lagrangian particle dispersion model

In order to simulate the impact of mesoscale wind fields and to assess potential capability of atmospheric Lagrangian particle dispersion model (LPDM) as an emergency response model for the decision supports, two different simulations of LPDM with the mesoscale prognostic model MM5 (Mesoscale Model ver. 5) were driven. The first simulation of radioactive noble gas ((85)Kr exponent) emitted during JCO accident occurred from 30 September to 3 October 1999 at Tokai, Japan showed that the first arriving short pulse was found in Tsukuba located at 60km away from the accidental area. However, the released radioactive noble gas was transported back to the origin site about 2 days later due to the mesoscale meteorological wind circulation, enhancing the levels of (85)Kr with the secondary peak in Tsukuba. The second simulation of atmospheric dilution factors (the ratio of concentration to the emission rate, chi/Q), during the underground nuclear test (UNT) performed by North Korea showed that high chi/Q moved to the eastward and extended toward southward in accordance with the mesoscale atmospheric circulations generated by mesoscale prognostic model MM5. In comparison with the measurements, the simulated horizontal distribution patterns of (85)Kr during the JCO are well accord with that of observation in Tsukuba such as the existence of secondary peak which is associated with the mesoscale circulations. However, the simulated level of (85)Kr anomaly was found to be significantly lower than the observations, and some interpretations on these discrepancies were described. Applications of LPDM to two mesoscale emergency response dispersion cases suggest the potential capability of LPDM to be used as a decision support model provided accurate emission rate of accident in case of a large accident.     

不同活性组分催化剂的氧化活性和热稳定性

采用流动法催化反应装置测定了蜂窝陶瓷负载催化剂同时催化氧化丙烷 ( C₃H₈)、丙烯 ( c₃H₆)和 CO的活性 ,考察活性组分 Pd和非贵金属氧化物、La改性、反应空速对起燃温度、热稳定性和动力学转化特征的影响 .结果显示 ,含 Pd催化剂上 C₃H₆和 CO的起燃温度比 C₃H₈低 ,1150℃高温老化对 C₃H₈氧化性能的影响比对 C₃H₆和 CO的小 .含稀土非贵金属氧化物的活性、热稳定性及动力学转化性能都比单 Pd催化剂低 ,添加 La能提高 2类催化剂的初活性和高温热稳定性 .     

TiO2光催化处理废水中贵重金属的研究进展

概述了TiO2光催化处理废水中贵重金属的原理、影响因素及应用研究.影响光催化处理水相中金属的因素包括TiO2的晶型、粒径和比表面积、TiO2的用量、改性剂、光源与光强、金属离子、溶液pH值、O2、空穴捕获剂、阴阳离子、固定化及光反应器.叙述了采用光催化法除去单一金属离子(Cr(Ⅵ)、Hg(Ⅱ)、Cd(Ⅱ))、选择性分离回收多种贵金属以及耦合协同处理金属与有机污染物.最后,指出了存在的问题及今后的研究趋势.     

Effect of pretreatment on Pd/Al2O3 catalyst for catalytic oxidation of o-xylene at low temperature

The effect of pretreatment on Pd/Al₂O₃ catalysts for the catalytic oxidation of o-xylene at low temperature was studied by changing the pretreatment and testing conditions. The fresh and pretreated Pd/Al₂O₃ catalysts were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The results showed that the pretreatment dramatically changed the Pd/PdO ratio and then significantly affected the Pd/Al₂O₃ activity; while the pretreatment had not much influence on Pd particle size. The Pd/Al₂O₃ pre-reduced at 300℃/400℃, which has fully reduced Pd species, showed the highest activity; while the fresh Pd/Al₂O₃, which has fully oxidized Pd species, presented the worst performance, indicating the Pd chemical state plays an important role in the catalytic activity for the o-xylene oxidation. It is concluded that metallic Pd is the active species on the Pd/Al₂O₃ catalyst for the catalytic oxidation of o-xylene at low temperature.     

Preparation of birnessite-supported Pt nanoparticles and their application in catalytic oxidation of formaldehyde

Flaky and nanospherical birnessite and birnessite-supported Pt catalysts were successfully prepared and characterized by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and N₂ adsorption-desorption. Effects of the birnessite morphology and Pt reduction method on the catalytic activity for the complete oxidation of formaldehyde (HCHO) were investigated. It was found that flaky birnessite exhibited higher catalytic activity than nanospherical birnessite. The promoting effect of Pt on the birnessite catalyst indicated that the reduction method of the Pt precursor greatly influenced the catalytic performance. Flaky birnessite-supported Pt nanoparticles reduced by KBH₄ showed the highest catalytic activity and could completely oxidize HCHO into CO₂ and H₂O at 50℃, whereas the sample reduced using H₂-plasma showed lower activity for HCHO oxidation. The differences in catalytic activity of these materials were jointly attributed to the effects of pore structure, surface active sites exposed to HCHO and the dispersion of Pt nanoparticles.     

TFJF型燃烧催化剂用于烘漆废气治理的研究

研制了一种贵金属－天然沸石／堇青石蜂窝体（ＴＦＪＦ）催化剂。通过实验室研究和部分漆包线石实际使用,考察了ＴＦＪＦ催化剂对漆包线机烘漆废气的治理效果。实验结果表明,对芳烃转化率为９８％的温度为１８０－２２０℃,甲酚为２２０－２４０℃;催化剂可８００℃以上的高温;实用结果表明,对烘漆废气良好的净化率,对二甲苯的去除率为９７％以上,出口浓度＜５０ｍｇ／ｍ＾３,同时不可以回收热能。