取代芳烃对酵母菌毒性的定量结构－活性相关研究

定量测定了苯胺类、苯甲酸类、卤代苯类、苯腈类、硝基苯类、苯酚类等６类化合物对酵母菌的生长抑制毒性，结果表明化合物的最小产生清晰抑菌圈浓度Ｃｍｉｚ与辛醇－水分配系数及一阶分子连接性价指数有如下关系：ｌｏｇ（１／Ｃｍｉｚ）＝０．３８ｌｏｇＫｏｗ＋０．３３＾１Ｘ＾ｖ－０．３８ ｒ＝０．９２ ｓ＝０．２２ ｎ＝７７。在上述６类取代苯类化合物中，它们与酵母菌的反应性大小有如下顺序：卤代苯类≈苯甲酸类〈苯胺类     

蚕豆根尖细胞微核法监测连云港市近海海水污染的研究

研究了用蚕虫根尖细胞微核技术监测海水污染的可行性，报告了用此法监测连云港市近海海水污染的实验结果。在与同期化学监测结果对比的基础上，提出了划分布污染等级的初步标准，对应用该法的意义进行了讨论。     

废弃混凝土再生利用的产业化研究

作为大规模城市化的产物,废弃混凝土引发了一系列的资源和环境问题.废弃混凝土的再生利用技术已经日趋成熟,而市场化推广却遇到成本、制度等方面的一系列难题.引入循环经济的理念,对废弃混凝土与再生混凝土进行成本比较、对产业化的困难和条件进行了剖析,并从技术、产业、经济等各方面提出了政策建议,也可为其它资源再生产业的发展提供一定的借鉴.     

论区际环境关系及其调控

区际环境关系是环境科学理论和实践研究的重要课题，随着生产力的发展，环境作为一种烯缺资源纳入人类的经济生活和社会生活中，由于存在局部环境利益的差异，不同区域的环境利益主体在追求利益最大化的驱动下，势必把环境成本转嫁与其他区域，这就促使原始的纯粹的区际自然关系发生深刻变化，新的区际环境关系发育和建立，文章认为，区际环境关系受社会经济诸多因素的影响，应从经济，法律和行政等多方面着手调控区际环境关系，建立科学，合理，公平的区际环境协作关系，以实现环境资源的集约化使用和生态环境问题的系统整治。     

模拟酸雨下土壤中稀土元素的环境化学行为和植物可利用性研究

研究了模拟酸雨对两种土壤中稀土元素的环境化学行为和植物可利用性的影响．结果表明，酸雨的酸度及淋洗量皆对稀土元素的淋溶产生影响，酸雨淋洗使土壤中稀土元素的形态含量发生了改变．由回归分析得知，有效态稀土的主要存在形态是交换态和松结有机态，实验表明，稀土的植物可利用性随模拟酸雨淋洗液的酸度增大而减小．     

Fluorescence spectroscopic studies of natural organic matter fractions

Because of the well-known molecular complexity and heterogeneity of natural organic matter (NOM), an aquatic bulk NOM was fractionated into well-defined polyphenolic-rich and carbohydrate-rich subfractions. These fractions were systematically characterized by fluorescence emission, three dimensional excitation-emission matrices, and synchronous-scan excitation spectroscopy in comparison with those of the reference International Humic Substances Society soil humic acid and Suwannee River fulvic acid. Results indicate that fluorescence spectroscopy can be useful to qualitatively differentiate not only NOM compounds from varying origins but also NOM subcomponents with varying compositions and functional properties. The polyphenolic-rich NOM-PP fraction exhibited a much more intense fluorescence and a red shift of peak position in comparison with the carbohydrate-rich NOM-CH fraction. Results also indicate that synchronous excitation spectra were able to provide improved peak resolution and structural signatures such as peak positioning, shift, and intensity among various NOM components as compared with those of the emission and excitation spectra. In particular, the synchronous spectral peak intensity and its red shift in the region of about 450-480 nm may be used to indicate the presence or absence of high molecular weight and polycondensed humic organic components, or the multicomponent nature of NOM or NOM subcomponents.     

日光/H_2O_2/草酸铁体系对垃圾渗滤液深度处理的试验研究

以草酸铁络合物/H2O2作光氧化剂,利用日光对垃圾渗滤生化出水进行了光氧化降解试验。结果表明,在溶液的初始体系pH=3.0,H2O2投加量为460mg/L,Fe3+质量浓度为20mg/L条件下,反应60min后,CODCr去除率可达80%以上;溶液初始体系的pH、H2O2和Fe3+的投加量及废水的水质对光解过程有显著影响,而且在太阳光照射下,CODCr去除率比紫外光照射下高。研究表明,在一定试验条件下,用日光/H2O2/草酸铁体系对城市垃圾渗滤液处理效果较好,可作为垃圾渗滤液的深度处理。     

水体pH和曝气方式对藻类生长的影响

利用水族箱微宇宙研究了藻类在不同pH和曝气条件下的生长和种类变化.使用天然湖水,一组试验每天调节pH,使其分别保持在8.0、8.5、9.0和9.5;另一组试验是设定不同的曝气方式,分别为不曝气、完全曝气、昼间曝气和夜间曝气,定期测定水体叶绿素a和藻类组成.pH试验结果显示,在pH 8.0～9.5范围内,pH 8.5下藻类生长状况最好,pH 9.5下生长最差,人为改变pH使其远离8.5能够抑制藻类生长.曝气试验结果显示,曝气不能抑制水体中藻类的生长,昼间曝气甚至还有明显的促进作用.     

TiO2/H2O2/UV和TiO2/O3/UV降解对氯苯甲酸和喹啉的试验研究

主要叙述TiO2/H2O2/UV和TiO2/O3/UV体系降解对氯苯甲酸(4-CBA)和喹啉的试验研究.研究表明,(1)在TiO2/H2O2/UV体系里目标物降解速度先随过氧化氢投加量的增加而提高,但超过一定浓度之后便开始下降;(2)在TiO2/O3/UV体系中,目标降解物的反应速度都非常快,且臭氧浓度高的时候降解速度更快;(3)二氧化钛催化剂在TiO2/O3/UV体系中作为积极因素有助于提高反应速率,而在TiO2/H2O2/UV体系是消极因素,会降低反应速率.     

Reaction-enhanced mass transfer and transport from non-aqueous phase liquid source zones

The objective of the following research is to theoretically quantify the enhancement of interphase mass transfer of dissolved non-aqueous phase liquid (NAPL) compounds from the non-aqueous phase to the aqueous phase and the enhancement of dispersive mass transport from a NAPL zone due to destruction of dissolved NAPL compounds. For relatively slow reaction rates, such as for permanganate and perchloroethene (PCE), local-scale mass transfer enhancement is expected to be small. Dispersive mass transport with reaction from a horizontal NAPL zone can be quantified using equations derived for a mathematically equivalent falling film reactor system. In contrast to local-scale interphase mass transfer, dispersive mass transport from NAPL zones may be significantly increased by reaction. Enhancement factors due to destruction of the NAPL compound(s) are mainly dependent on NAPL solubility and oxidant concentration and to a lesser extent on reaction rate, stoichiometry, and transverse dispersion coefficients. Higher NAPL solubility and/or lower oxidant concentration reduces the maximum expected enhancement factor. Reaction enhancement factors for mass transport from NAPL zones are expected to be in the range of 5-50 for permanganate and chlorinated solvents. Theoretical results suggest that assuming instantaneous reaction rates may be appropriate for dispersive mass transport from NAPL zones.