舍铁固废千法生产氧化铁红新工艺技术研究

针对冶金企业在生产过程中发生的含铁尘泥,提出了与之相适应的处理新工艺。利用部分种类的尘泥成功制取了符合磁性材料行业要求的氧化铁红,并广泛应用于磁材预烧料企业,从而为含铁尘泥的综合利用提供了新的思路和有效途径。     

南京市不同功能城区土壤中重金属Cu、Zn、Pb和Cd的污染特征

将南京城市建成区分为矿冶区、开发区、商业区、城市广场、风景区、老居民区等6大功能区,选择采集土壤样本56个,用原子吸收光谱仪选择分析了土壤中重金属元素的全量和活性形态含量.结果表明,南京城市土壤中Pb、Cu、Zn和Cd的总量分别为:117.1±103.7mg·kg^-1,39.86±39.9mg·kg^-1,273.3±131.6mg·kg^-1和1.13±0.7mg·kg^-1.矿冶区、老居民区、商业区、新开发区、城市广场和风景区的内梅罗重金属综合污染指数分别为:5.4、4.9、3.4、1.6、2.4和2.3.矿冶区以Pb、Cd的强度积累为特征,但活性形态的比重较小.而城市中心的居民区和商业区Zn的积累最显著,并且所测定的重金属的醋酸盐浸提态含量明显较高.除了风景区和城市市民广场外,城市中心区的重金属均表现出较明显的表聚性.城市活动区土壤Pb、Cd的强烈积累可能已经对人类健康构成了威胁.     

微电解-UASB-接触氧化处理酚醛树脂废水

采用微电解一上流式厌氧污泥床（Upflow Anaerobic Sludge Bed,简称UASB）-接触氧化工艺处理酚醛树脂生产废水（简称废水）。实验结果表明：采用微电解法对废水进行预处理,不仅去除了约36％COD,还大幅度提高了废水的可生化性;微电解出水经UASB厌氧生物处理后,COD去除率达80％;水解酸化COD去除率约为30％;最后经二级接触氧化处理,出水COD为100mg／L以下,达到GB8978--1996《污水综合排放标准》中化工类废水的二级排放标准。     

UV/H2O2工艺降解水中双酚A影响因素的研究

研究了UV/H2O2工艺对双酚A(BPA)的降解效果及影响田素.结果表明,UV/H2O2工艺可以有效降解水体中BPA,降解过程符合一级反应动力学模型;紫外光强对BPA的降解速度影响较小;H2O2浓度对BPA的降解具有促进和抑制的双重作用;BPA初始浓度对BPA降解没有影响;在酸性条件下,有利于BPA降解;NO-3、Cl-、HCO-3对BPA降解有抑制作用;当HCO-3、NO-3、Cl-摩尔浓度均为5mmol/L时,对BPA降解的抑制程度为HCO-3>NO-3>Cl-.腐殖酸在低浓度时,促进BPA降解反应进行;在高浓度时,BPA的降解受到抑制.     

高压电晕与臭氧联用对不同结构染料脱色效果的比较研究

比较研究了高压电晕与臭氧联用对活性艳红X-3B(单偶氮)、活性艳蓝X-BR(蒽醌)、活性黑KN-GRRC(双偶氮)、酸性红ARL(单偶氮)、酸性蓝BRL(蒽醌)、酸性橙AGT(双偶氮)和分散蓝2BLN(蒽醌)7种染料模拟废水的脱色效果.结果显示,酸性橙AGT模拟废水的脱色速度较慢,而其他6种染料在15 min内都能完全脱色,这表明染料结构本身的差异决定了脱色效果;活性染料模拟废水的脱色效果优于酸性染料;蒽醌染料和单偶氮染料模拟废水的脱色效果明显好于双偶氮染料.     

绿色有机电合成与可持续发展

综述了有机电合成的发展状况、基本原理及优点,阐述了有机电合成技术在实施“绿色化工”战略过程中的重要作用及主要应用领域,论述了有机电合成与可持续发展的关系。     

乳状液膜法处理含柠檬酸工业废水的研究

本文研究了以LMA-1为表面活性剂,正三辛胺为流动载体,Na_2CO_3溶液为内相试剂.煤油为膜溶剂所组成的液膜体系处理柠檬酸废水,考察了搅拌速度、表面活性剂种类和用量.载体用量、乳水比、油内比对废水中COD去除率的影响,结果表明:当LMA-1为3g·100ml~(-1)煤油,R_(?)=1:10,R_(?)=1:1.搅拌速度为300r·min~(-1)时.废水中COD的去除率可达99%.     

O(~1D)与CF_2CIBr的反应研究

本文研究了CF_2ClBr-O_3体系在253.7nm紫外光照下所引发的O(~1D)与CF_2ClBr的反应.O(~1D)与CF_2ClBr反应的最终产物为CF_2O,Cl_2,Br_2;实验中得到O(~1D)与CF_2ClBr的反应速率常数为1.01×10~(-10)cm~3·molecule~(-1)·s~(-1),并且对O(~3P)与CF_2ClBr的反应可能性以及 O(~1D)与CF_2ClBr的反应机理进行了讨论.     

上海市大气中HO2自由基的测定与特征

为研究上海市大气中ＨＯ２自由基的分布特征,建立了化学放大法测定ＨＯ２自由基系统,对上海市大气中ＨＯ２自由基浓度进行了没定邦等结果表明,ＨＯ２自由基的典型日变化基本上为双峰型,峰值出现在阳光辐射较强的中午时分,实验测得ＨＯ２自由基最大浓度达２．２４×１０＾８分子·ｃｍ＾－３,ＨＯ２自然基民ＮＭＨＣ,Ｃ烽Ｏ２等具有一定的相关性,ＨＯ２自由基的研究对于大气光化学烟雾的研究具有重要意义     

Adsorption behavior of imidacloprid pesticide on polar microplastics under environmental conditions: critical role of photo-aging

● Small molecular chains formed on photo-aged polylactic acid microplastics (MPs). ● Oxygen-containing functional groups generated on photo-aged polyamide MPs. ● Photo-aging has the opposite influence on the imidacloprid adsorption on two MPs. ● Electrostatic interactions and hydrogen bonds were the main mechanisms. ● High pH value and low ionic strength increase the adsorption capacity. The photo-aging behavior of microplastics (MPs) in natural environment has become a global concern. The ultraviolet radiation has enough energy to change the polymer structure and physical-chemical properties of MPs. Less attention has focused on the interactions of the photo-aged polar and biodegradable MPs with organic pollutants. This work investigated the structural properties of aged polar polyamide (PA) MPs and biodegradable polylactic acid (PLA) MPs exposed to ultraviolet irradiation and their adsorption behavior and mechanism for neonicotinoid insecticide imidacloprid (IMI). The results showed that the MPs had extensive changes in surface morphology and chemical properties after photo-aging. The C–N bond of PA MPs was disrupted to form more carbonyl groups. The oxygen-containing functional groups on the surface of aged PLA MPs were broken and generated relatively smaller molecules. The adsorption capacity of IMI on PA MPs decreased by 19.2 %, while the adsorption capacity of IMI on PLA MPs increased by 41.2 % after photo-aging. This depended on the natural structure of the MPs and their ability to absorb ultraviolet light. The electrostatic interactions, hydrogen bonds, van der Waals interactions, and polar-polar interactions were the main adsorption mechanisms of IMI on MPs. High initial solution pH and low ionic strength favored the adsorption of IMI by altering charge distribution on the MPs surface. The formation of the humic acid-IMI complexes decreased the concentration of IMI in the water phase and further decreased the adsorption on MPs. These results are enlightening for a scientific comprehension of the environmental behavior of the polar MPs.