Long term changes in atmospheric N and S throughfall deposition and effects on soil solution chemistry in a Scots pine forest in the Netherlands

In a Scots pine forest the throughfall deposition and the chemical composition of the soil solution was monitored since 1984. (Inter)national legislation measures led to a reduction of the deposition of nitrogen and sulphur. The deposition of sulphur has decreased by approximately 65%. The total mineral-nitrogen deposition has decreased by ca. 25%, which is mainly due to a reduction in ammonium-N deposition (−40%), since nitrate-N deposition has increased (+50%). The nitrogen concentration in the upper mineral soil solution at 10 cm depth has decreased, leading to an improved nutritional balance, which may result in improved tree vitality. In the drainage water at 90 cm depth the fluxes of NO₃⁻ and SO₄²⁻ have decreased, resulting in a reduced leeching of accompanying base cations, thus preserving nutrients in the ecosystem. It may take still several years, however, before this will meet the prerequisite of a sustainable ecosystem.     

大气微生物与气象条件及大气污染物的灰色关联分析

根据大气微生物浓度、气象因子和大气污染理化因子的监测结果，应用灰色关联分析原理，分析研究大气微生物浓度与气象条件和大气污染物的关联程度，说明气象因子对各类微生物浓度的影响大于大气污染因子，特别是对耐高渗透压霉菌。     

天然浑浊水中共存无机阳离子的电动化学特征

引入流动电流这一重要电动化学参量，研究了在天然浑浊水中ＳＣ的基本模式，撮了ＳＣ与水中悬浮胶体颗凿表面电荷量及无机阳离子之间的理论关系，探讨了离子的浓度，性质，存在环境等对体系电动特性的影响，并对水中常见８种阳离子共存条件下的电动化学特性进行了实验分析，从而建立了无机阳离子对胶体的聚沉能力与电动响应特性之间的实际联系。     

Role of water chemistry on estrone removal by nanofiltration with the presence of hydrophobic acids

Hydrophobic acid organic matter (HpoA) extracted from treated effluent has been known to improve the rejection of steroid hormone estrone by reverse osmosis (RO) and nanofiltration (NF) membranes. In this study, the effects of solution chemistry (solution pH and ionic strength) on the estrone rejection by NF membrane with the presence of HpoA were systematically investigated. Crossflow nanofiltration experiments show that the presence of HpoA significantly improved estrone rejection at all pH and ionic strength levels investigated. It is consistently shown that the “enhancement effect” of HpoA on estrone rejection at neutral and alkaline pH is attributed to the binding of estrone by HpoA macromolecules via hydrogen bonding between phenolic functional groups in feed solutions, which leads to an increase in molecular weight and appearance of negative charge. The membrane exhibited the best performance in terms of estrone rejection at pH 10.4 (compared to pH 4 and pH 7) as a result of strengthening the electrostatic repulsion between estrone and membrane with the presence of HpoA. At neutral pH level, the ability of HpoA macromolecules to promote estrone rejection became stronger with increasing ionic strength due to their more extended conformation, which created more chances for the association between estrone and HpoA. The important conclusion of this study is that increasing solution pH and salinity can greatly intensify the “enhancement effect” of HpoA. These results can be important for NF application in direct/indirect potable water reuse.     

土壤重金属的植物污染化学研究进展

针对中国土壤重金属污染加剧的趋势,为改善土壤环境质量和保障农产品安全,提出了土壤重金属的植物污染化学研究领域.结合多年的研究工作,从土壤重金属的植物根际化学行为、土壤重金属的植物吸收与解毒机制和重金属污染土壤的植物-微生物交互作用等方面简要阐述了土壤-植物系统中重金属的分布、存在形态、迁移转化、累积及生物学效应和控制规律的研究进展,并对将来的植物污染化学理论研究提出了展望.     

空气质量数值模型的构建及应用研究进展

综述了近年来国内外空气质量模型的发展历程、空气质量数值模型构建的关键技术以及应用研究。指出了目前空气质量数值预报及应用主要面临气象条件,尤其是大气边界层模拟、大气污染物排放源和大气物理化学过程等问题。提出,应当通过规范化制作和完善排放源清单数据,建立统一的排放源分析标准,提高排放源数据的准确性;多向发展观测手段,加大监测密度和频率,并进行实验室化学分析,提出适合我国的大气物理化学机制。就空气质量模式而言,对模式方案进行优化,以及使用气象、卫星资料同化等技术手段,将其与观测相结合,构建监测与预报系统相结合的统一体系,应用于多平台。     

石油化工装置污染源分析

对石油化工行业三大典型工艺,即炼油、乙烯和化纤的污染源产生情况及特性进行分析,找出不同装置废气、废水、固体废物等污染源产生的特点和共性,以利于石油化工项目的环境影响评价工作中污染源产生情况的准确分析和评价。     

土壤重金属污染及其修复技术研究

土壤重金属污染物有汞、镉、铅、锌等,主要来源于交通运输、工业污染和农业污染。土壤重金属污染会导致农作物减产甚至死亡,对人体健康也会产生极大危害。目前土壤重金属污染修复的技术主要包括工程修复法、物理化学修复法、化学修复法和生物修复法。植物修复技术作为一种新兴的绿色、生态、高效的修复技术具有良好的发展前景。     

一种快速检测甲胺磷的方法

由于农药的不合理利用以及对检测速度的要求,本文应用水溶性碳化二亚胺(EDC)法将甲胺磷与BSA连接,合成了免疫抗原,经紫外扫描确定免疫抗原连接成功.用合成的免疫抗原免疫实验用大白兔,制备了甲胺磷的多克隆抗血清,效价达到1:1000000以上.经盲样检验,抗体灵敏性和特异性较好;在检测样品时最低检测极限为0.5 ng/g,达到国际同类检测试剂盒的水平;且可以在1.5 h内检测100多个样品.     

OH自由基降解二英OCDD的反应机理及动力学研究

采用量子化学计算研究了OH自由基降解八氯代二苯并对-二英（OCDD）的微观反应机理,计算分析了微观反应进程,结果表明该反应存在两条途径：①α-氯取代：1,4,6,9位置氯取代,该路径反应活化能较高,反应难以进行,并以中间产物积聚,无法使OCDD的毒性消失;②β-氯取代：2,3,7,8位置氯取代,该路径的反应能相对较低,且能使OCDD的毒性消失,是有效降解OCDD的主要途径.结合过渡态理论,计算获得动力学参数：反应活化能为8.32 kJ·mol^-1（B3LYP/6-311G++（d,g）//B3LYP/6-31G（d））,阿仑尼乌斯表达式为k=1.29×10¹⁴exp（-1049.6/T）（cm³·mole^-1·s^-1）.这与文献实验结果取得了很好的吻合,说明本文对OH自由基降解OCDD的反应机理及动力学研究是合理且可靠的.本文的计算结果可为催化氧化降解二英的进一步研究提供理论参考.