水解-好氧工艺处理生活污水

采用水解 好氧工艺 ,替代了WSZ F地埋式设备处理生活污水。既解决了设备腐蚀 ,又克服了停留时间不足的问题 ,同时提高了处理效果。     

富马酸废水降解菌的选育及降解效果

针对富马酸废水,从活性污泥中筛选出降解富马酸废水的降解菌,通过分离纯化,优选出四株适应能力强、生长旺盛的菌株,分别为FH-1、FH-2、TFH-1、TFH-2。经初步鉴定分别为隐球酵母属、节细菌属、微球菌属、假单胞菌属。试验测定了单株菌和混合菌对富马酸废水的降解效果,结果表明混合菌的降解效果最为明显,降解率为74.9%。     

论聚烯烃裂解反应中的油化效果增强效应

在废旧聚烯烃的裂解反应中,聚丙烯的存在,可以提高轻油馏份的收率,增强反应的油化效果,本文称之为聚烯烃裂解反应的增强效应。本文讨论了增强效应产生的机理,可为废旧塑料裂解油化技术的研究和开发提供参考。     

散射光下铁(Ⅲ)-丙酮酸盐配合物还原铬(Ⅵ)的研究

研究了在散射光下铁（Ⅲ）-丙酮酸盐配合物对铬（Ⅵ）的光还原反应;考察了溶液pH、铁（Ⅲ）、丙酮酸钠、铬（Ⅵ）浓度对反应的影响;分析了铬（Ⅵ）光还原反应的动力学。实验结果表明：铁（Ⅲ）-丙酮酸盐配合物体系能在较弱的散射光下还原铬（Ⅵ）。在铬（Ⅵ）浓度为19．2μmol／L、铁（Ⅲ）浓度为10．0μmol／L、丙酮酸钠浓度为240μmol／L、pH为3．0、光照240min的条件下,铬（Ⅵ）的还原率达到99．7％。从表观动力学方程的反应级数看,铁（Ⅲ）的级数（0．83）最高,铁（Ⅲ）浓度是影响铬（Ⅵ）光还原反廊速率的主要因素．铁（Ⅱ）是铬（Ⅵ）光还原的主要还原剂。     

植物提取液处理恶臭气体的研究进展

介绍了近二十年来国内外关于植物提取液治理恶臭气体的研究成果,内容包括植物提取液的应用研究、除臭机理研究及植物提取液提取方法的研究;指出对恶臭气体中的胺类和醚类除臭机理、对植物提取液提取工艺优化的研究是今后研究的重点。     

聚乙烯醇/氧化石墨插层纳米复合材料的结构和热分析

制备了聚乙烯醇/氧化石墨插层纳米复合材料,并用X-射线衍射仪和高分辨电镜对其结构进行了表征.X-射线衍射仪和高分辨电镜的试验结果表明,氧化石墨和聚乙烯醇插层氧化石墨的层间距分别为0.89 nm和1.4nm.该纳米复合材料的热分析和热失重图说明,氧化石墨的加入有利于提高聚乙烯醇/氧化石墨纳米复合材料的玻璃化转变温度和氧化温度,同时也降低了其热释放速率.     

生物絮凝剂MBFGA1预处理乳制品加工废水

用生物絮凝剂MBFGA1预处理乳制品加工废水（简称废水）。实验结果表明,废水处理的水力条件为：以150r／min的转速搅拌30S,再以30r／min的转速搅拌20min;MBFGA1的最佳加入量为15mg／L;废水pH为4．0时,MBFGA1对废水的絮凝处理效果最好;废水温度对浊度、COD去除率有一定的影响,在20～45℃时,废水浊度的去除率始终保持在85％以上;30℃时,COD去除率达到最大值65．0％。     

邹平县大气降水酸度影响因素分析

应用灰色理论,以2002,2003,2004,2005,2006连续五年为时间序列点,取大气降水pH值为参考因素,取大气中SO2、NOx、TSP、降尘的浓度为比较因素进行关联分析。灰关联度矩阵表明：邹平县大气降水酸度的最大影响因素是SO2,其次降尘的影响也不容忽视。     

Reaction pathways of dimethyl phthalate degradation in TiO2-UV-O2 and TiO2-UV-Fe(VI) systems

The photocatalytic degradation of dimethyl phthalate (DMP) in aqueous TiO₂ suspension under UV illumination has been investigated using oxygen (O₂) and ferrate (Fe(VI)) as electron acceptors. The experiments demonstrated that Fe(VI) was a more effective electron acceptor than O₂ for scavenging the conduction band electrons from the surface of the catalyst. Some major intermediate products from DMP degradation were identified by HPLC and GC/MS analyses. The analytical results identified dimethyl 3-hydroxyphthalate and dimethyl 2-hydroxyphthalate as the two main intermediate products from the DMP degradation in the TiO₂–UV–O₂ system, while in contrast phthalic acid was found to be the main intermediate product in the TiO₂–UV–Fe(VI) system. These findings indicate that DMP degradation in the TiO₂–UV–O₂ and TiO₂–UV–Fe(VI) systems followed different reaction pathways. An electron spin resonance analysis confirmed that hydroxyl radicals existed in the TiO₂–UV–O₂ reaction system and an unknown radical species (most likely an iron–oxo species) is suspected to exist in the TiO₂–UV–Fe(VI) reaction system. Two pathway schemes of DMP degradation in the TiO₂–UV–O₂ and TiO₂–UV–Fe(VI) reaction systems are proposed. It is believed that the radicals formed in the TiO₂–UV–O₂ reaction system preferably attack the aromatic ring of the DMP, while in contrast the radicals formed in the TiO₂–UV–Fe(VI) reaction systems attack the alkyl chain of DMP.     

A directional passive air sampler for monitoring polycyclic aromatic hydrocarbons (PAHs) in air mass

A passive air sampler was developed for collecting polycyclic aromatic hydrocarbons (PAHs) in air mass from various directions. The airflow velocity within the sampler was assessed for its responses to ambient wind speed and direction. The sampler was examined for trapped particles, evaluated quantitatively for influence of airflow velocity and temperature on PAH uptake, examined for PAH uptake kinetics, calibrated against active sampling, and finally tested in the field. The airflow volume passing the sampler was linearly proportional to ambient wind speed and sensitive to wind direction. The uptake rate for an individual PAH was a function of airflow velocity, temperature and the octanol-air partitioning coefficient of the PAH. For all PAHs with more than two rings, the passive sampler operated in a linear uptake phase for three weeks. Different PAH concentrations were obtained in air masses from different directions in the field test.