序列间歇式好氧活性污泥法处理生物制药废水研究

本研究采用好氧ＳＢＲ法处理生物制药废水。试验结果表明，废水中不需另加氮磷营养物质，当进水ＣＯＤＣｒ为９１１～３２８０ｍｇ／Ｌ时，在曝气１６ｈ条件下，出水ＣＯＤＣｒ在３５０ｍｇ／Ｌ以下，ＢＯＤ５在８０ｍｇ／Ｌ以下，ＳＳ在１５０ｍｇ／Ｌ以下，皆达到生物制药工业废水二级排放标准。本文还对好氧ＳＢＲ法的有机物降解动力学过程进行了研究。     

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.     

太阳光助Fenton体系氧化降解苯酚废水的研究

探讨了太阳光助Fenton体系对苯酚的氧化降解。结果表明，太阳光能有效地增强Fenton试剂对苯酚的氧化降解，在晴天较强太阳光照下，Fenton试剂可在较短时间内使较高浓度的苯酚完全矿化。反应体系的初始pH值及Fe^2 用量均对苯酚的氧化降解有明显影响，反应的适宜pH值在3—4的酸性范围内；适量Fe^2 参与的太阳光—Fenton反应有助于苯酚的降解，但过高的Fe^2 用量反而不利于苯酚的降解。实验结果还表明，采用分批多次投加的方式可明显提高氧化剂H202的利用效率，降低H202的消耗量；苯酚废水降解的主要中间产物为苯醌和有机酸；一定程度的太阳光—Fenton预氧化处理可使废水的BOD5／C02cr比值由0.10捉高到0.32，可生化性明显提高。     

催化技术在污染物治理应用的研究进展

对近年来催化技术在污染物治理应用的研究进展进行了综述,指出了现在研究中存在的主要问题,并对其前景进行了展望。     

Catalytic dechlorination of chlorobenzene in water by Pd/Fe bimetallic system

IntroductionChlorinatedorganiccompoundshavebeenusedonalargescaleinthechemical,petrochemical,andelectronicindustries.Inrecentyears ,worldwideattentionhasbeengiventotheenvironmentalandhealthimpactofthemasaclassofcontaminants .Severalareknowntocauseozonedepletion ,whileothersproduceadverseeffectsonthehumancentralnervoussystemandhavebeenlinkedtodiseasessuchascancer.Almostallofthechlorinatedaromaticcompoundsaretoxicandthermallystable .Oncereleasedintoenvironment,theywillaccumulateinthesurroundings…     

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.     

催化裂化废水连续萃取脱酚研究

选用焦化粗柴油为萃取剂，在转盘萃取搭连续试验装置中，对催化裂化含酚废水进行脱酚预处理。结果表明，用焦化粗柴油做萃取剂，进水ｐＨ值为８０～９０不加调节；油水比（体积比）１７∶１～２１∶１；转盘转数１１００ｒ／ｍｉｎ，酚萃取脱除率达到８５％以上。萃取后的粗柴油依据现有工艺而进行加氢精制，不需进行再生等后处理。整个萃取工艺简单易行，能满足预处理的要求     

4—氯苯甲酸钠的光催化氧化降解及其影响因素

本试验采用P－25TiO2，光催化剂，对4－氯苯甲酸钠的光催化氧化降解及污染物初始浓度，催化剂投加量和入射光强等因素的影响进行了研究，研究发现污染物初始降解速率与其初始浓度的关系遵循Langmuir-Hinshelwood模式，其中半饱和浓度常数Ks不仅是催化剂和污染物种类的函数，而且也是入射光强的函数，催化剂投加量存在一限值，当低于此限值时，污染物降解速率由于催化剂浓度的不足受到影响而下降，当高于此限值时，污染物降解速率受催化剂投加量的影响变小，在本试验4－CBA－Na浓度为0.15-0.6mmol／L时该催化剂限值浓度大约为0.4g/L，在入射光强为1-7mW/cm^2和催化剂浓度为0.4g／L下，污染物降解速率与光强成0.67次幂关系，经估算其量子效率为6．3％。     

土壤中嗪草酮迁移和降解的研究

 通过两季马铃薯大田试验，研究了嗪草酮在灌溉沙壤土中的消失和移动情况。结果表明，表层土壤中，嗪草酮施用后最初7～15天内其含量急剧降低，此后随时间推移降低幅度平缓，1993年和1994年试验结束时的残留量分别为5.9μg/kg和2.3μg/kg。两年共采集的379个土样（分布在15～75cm各土层）中只有5个检测到有嗪草酮。1994年大田135cm土层处的水样中，嗪草酮的检测率高达66％，检测浓度范围为0.06～15.85μg/kg，平均浓度为1.94μg/kg。相比较，嗪草酮在大田试验中的消失速率远大于实验室控制条件下的降解速率。