区际生态环境关系理论初探——兼论江苏省与周边省市的环境冲突与合作

区际生态环境关系是随着区域生态环境利益冲突不断加剧,区域之间逐步形成的一种与经济关系、社会关系紧密相关而又相互区别的新型关系。对区际生态环境关系这一环境科学论题进行了理论阐述,初步探讨了区际生态环境关系的内涵、特征、主要内容和分类,以及区域环境合作与冲突等基本问题,着重提出了区际环境冲突的形式、成因与解决机制,试图从区域间环境的矛盾冲突这个新的视角去认识区域环境问题,探索解决区域环境问题和区际环境矛盾的新途径。以江苏省为例,初步探讨了江苏省与周边省、市的环境矛盾冲突以及建立省际环境合作的机制与对策,认为江苏省位于长江和淮河等流域下游,周边环境状况并不乐观,同时又是资源、能源的输入和消耗大省,随着社会经济的发展,省际生态环境利益冲突将会进一步显现,因此应加强与其他省市的资源、环境合作,以解决日益严峻的区域生态环境问题     

近60a长三角地区极端高温事件变化特征及其对城市化的响应

基于长三角地区1951~2014年56个国家级气象站点逐日气温记录资料,通过计算极端高温事件相关指标(极端最高温TXx,极端最低温TNn,高温日数Htd和低温日数Ltd),利用GIS空间分析技术和Mann-Kendall时间趋势分析方法分析了长三角地区近60 a极端高温事件的空间分异特征和时间变化趋势,并探讨了城市化发展对区域极端高温事件时空变异的影响。结果表明:(1)长三角地区极端高温事件指标均表现为一定的上升趋势,极端低温指标(TNn和Ltd)线性变化趋势比极端高温指标(TXx和Htd)更为显著,变化趋势最显著的地区集中在经济和城市化水平较高的城市及周边地区(如上海、杭州等)。(2)极端高温指标(TXx和Htd)多年平均总体表现为南高北低,西高东低的趋势,而极端低温指标中TNn多年平均为由中部向南北两侧降低,Ltd多年平均呈现自中部向南北南侧增多的趋势。(3)从1990~2000到2000~2010年,城市化对极端高温事件的影响增强,快速城市化对北部城市极端高温事件的影响高于南部城市。     

沸石联合微生物固定化去除微污染水体中氨氮的研究

将沸石联合经过驯化的活性污泥微生物固定化,通过静态实验.考察了不同粒径沸石及不同组分固定化方法对沸石联合微生物固定化去除氨氮的影响;通过动态实验,考察了沸石联合微生物固定化去除微污染水体中低浓度氨氮的机制.结果表明,活性污泥经过16 d的驯化,氨氮去除率为90%以上;沸石吸附氨氮为快速吸附,粒径<0.5 mm的沸石的吸附容量明显大于其他粒径的沸石;不同组分固定化小球对氨氮的去除效率不同,各组分均有贡献,吸附容量依次为:沸石固定化小球>沸石联合微生物固定化小球>微生物固定化小球;沸石联合微生物固定化去除微污染水体中低浓度氨氮可分为4个阶段,即沸石吸附阶段、吸附饱和及微生物适应阶段、硝化作用明显加强和沸石部分再生阶段、微生物作用良好和沸石进一步再生阶段,最终沸石吸附与生物再生处于良好的动态平衡中,氨氮去除率达到60%左右.     

Part V—sorption of pharmaceuticals and personal care products

Background, aim, and scope  Pharmaceuticals and personal care products (PPCPs) including antibiotics, endocrine-disrupting chemicals, and veterinary pharmaceuticals are emerging pollutants, and their environmental risk was not emphasized until a decade ago. These compounds have been reported to cause adverse impacts on wildlife and human. However, compared to the studies on hydrophobic organic contaminants (HOCs) whose sorption characteristics is reviewed in Part IV of this review series, information on PPCPs is very limited. Thus, a summary of recent research progress on PPCP sorption in soils or sediments is necessary to clarify research requirements and directions. Main features  We reviewed the research progress on PPCP sorption in soils or sediments highlighting PPCP sorption different from that of HOCs. Special function of humic substances (HSs) on PPCP behavior is summarized according to several features of PPCP–soil or sediment interaction. In addition, we discussed the behavior of xenobiotic chemicals in a three-phase system (dissolved organic matter (DOM)–mineral–water). The complexity of three-phase systems was also discussed. Results  Nonideal sorption of PPCPs in soils or sediments is generally reported, and PPCP sorption behavior is relatively a more complicated process compared to HOC sorption, such as the contribution of inorganic fractions, fast degradation and metabolite sorption, and species-specific sorption mechanism. Thus, mechanistic studies are urgently needed for a better understanding of their environmental risk and for pollution control. Discussion  Recent research progress on nonideal sorption has not been incorporated into fate modeling of xenobiotic chemicals. A major reason is the complexity of the three-phase system. First of all, lack of knowledge in describing DOM fractionation after adsorption by mineral particles is one of the major restrictions for an accurate prediction of xenobiotic chemical behavior in the presence of DOM. Secondly, no explicit mathematical relationship between HS chemical–physical properties, and their sorption characteristics has been proposed. Last but not least, nonlinear interactions could exponentially increase the complexity and uncertainties of environmental fate models for xenobiotics. Discussion on proper simplification of fate modeling in the framework of nonlinear interactions is still unavailable. Conclusions  Although the methodologies and concepts for studying HOC environmental fate could be adopted for PPCP study, their differences should be highly understood. Prediction of PPCP environmental behavior needs to combine contributions from various fractions of soils or sediments and the sorption of their metabolites and different species. Recommendations and perspectives  More detailed studies on PPCP sorption in separated soil or sediment fractions are needed in order to propose a model predicting PPCP sorption in soils or sediments based on soil or sediment properties. The information on sorption of PPCP metabolites and species and the competition between them is still not enough to be incorporated into any predictive models.     

环糊精聚合物对苯胺的吸附和脱附性能研究

以环氧氯丙烷为交联剂,合成和表征了β-环糊精聚合物(β-CDP),从动力学和热力学角度研究了β-CDP对苯胺的吸附性能。研究结果表明,β-CDP对水溶液中的苯胺具有一定的吸附量。用Langmuir, Freundlich和DubininRadushkevich(D-R)吸附等温式拟合了平衡等温数据,并计算出每个模型的参数。苯胺在β-CDP上的吸附符合D-R方程,吸附过程是热力学自发行为。在乙醇中,β-CDP的脱附能力很强,且可循环使用多次。     

我国旅游景区经营模式的构想

本文以旅游景区的经营模式为研究核心,从现有国内外旅游景区组织结构分析入手,构建了适合我国国情和旅游景区可持续发展要求的两种经营模式：一种是国有国营的次国家公园模式,另一种是完全企业化经营,并且提出了两种模式运作的保障条件。     

四氯化钛精制除钒废弃物的综合利用

对四氯化钛铜丝除钒精制过程中产生的废弃物,采用酸碱联合法回收其中的铜和钒。考察了关键的碱处理及盐酸沉钒过程的影响因素。实验结果为：在碱处理溶液pH12．0—13．0,碱处理温度60℃,碱处理时间1h,沉钒溶液pH1．0～1．5,沉钒温度60℃,沉钒时间1h的条件下,铜和钒的回收率分别达到90％和75％以匕,获得的阴极铜和五氧化二钒的产品质量均达到国家标准。     

河流沉积物中有机污染物的分析研究进展

总结了近年来河流沉积物中有机污染物的研究进展 ,集中评述了国内有关沉积物中多环芳烃、有机氯农药和多氯联苯的分析研究现状 ,包括样品采集、样品前处理和样品分析 ,并对今后河流、湖泊及水库沉积物中污染物的分析工作作了展望     

江苏省环境监测现代化建设的设想

从环境监测现代化建设的目标、原则、内容、资源配置及保证措施等方面,阐述了江苏省环境监测现代化建设的具体设想.提出用3年～5年的时间,实现该省环境监测实时监控系统的自动化、实验室分析技术的现代化、环境监测信息技术的网络化及环境监测体制的多元化和管理机制的市场化,建成能适应市场经济体制,满足科学管理需要,具备国际先进技术和国际间互认能力的环境监测网络体系.     

Degradation of octylphenol and nonylphenol by ozone - part I: direct reaction

This aqueous reaction between ozone and two alkylphenols (APs), namely octylphenol (OP) and nonylphenol (NP), has been investigated. Both compounds are important endocrine disrupting chemicals, which arise from the biodegradation of alkylphenol ethoxylates and are often found at relatively high concentrations in wastewater effluents. In this paper the results of an experimental study are presented which provide values for the reaction rate constants between molecular ozone and undissociated OP and NP, and overall reaction rate constants for the degradation of the two APs at pH values in the range of 7-9. The kinetic rate constants for OP and NP degradation by molecular ozone were 4.33(+/-0.18) x 10(4) and 3.90(+/-0.10) x 10(4) M(-1) s(-1), and the reaction stoichiometry was similar in both cases and equal to approximately 1.3:1 ([O3]:[AP]). The overall second order reaction rate constants for the two APs increased significantly with increasing pH, which is believed to be mainly due to the increasing influence of indirect radical reaction with increasing pH; this aspect is considered in more detail in a companion paper. A preliminary investigation of the reaction mechanism suggests that an initial product of ozonation is hydroxyl-alkyl phenol.