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201.
H. S. Lin H. D. Scott K. F. Steele H. I. Inyang 《Environmental monitoring and assessment》1999,58(2):151-172
Statistical methods and a Geographic Information System (GIS) were used to investigate potential indicators of ground water vulnerability to agricultural chemical contamination in a representative area of the Mississippi River alluvial aquifer. A total of 47 wells were sampled for analysis of nitrate, phosphorus, potassium, and 13 pesticides commonly-used in the area. Ten soil and hydrogeologic variables and five ground water vulnerability indices were examined to explain the variations of chemical concentrations. The results showed that no individual soil or hydrogeologic variables or their linear combinations could explain more than 25% of the variation of the chemical concentrations. A quadratic response surface model with the values of confining unit thickness, slope, soil permeability, depth to ground water, and recharge rate accounted for 62% of the variation of nitrate, 43% of P, and 83% of K, suggesting that the interactions among soil and hydrogeologic variables were significant. Observed trends of decreasing nitrate and P concentrations with increasing well depth and/or depth to ground water seemed to correlate with carbonate equilibrium in the aquifer and more reduced environment with depth. In view of uncertainties involved, it was recognized that the limitations associated with input data resolution used in GIS and the formulation of leaching indices limited their use for predicting ground water vulnerability. Misuse of pesticides could be another factor that would complicate the relationships between pesticide concentrations and the vulnerability indices. 相似文献
202.
Samaratunga SS Nishimoto J Tabata M 《Environmental science and pollution research international》2008,15(1):27-30
BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples. 相似文献
203.
超临界水氧化中设备腐蚀的研究现状 总被引:2,自引:0,他引:2
超临界水氧化(SCWO)技术是近年发展起来的处理有机难溶废物的安全高效的新技术。在阐述超临界水的物理、化学性质的基础上,介绍了SCWO反应的工作原理和流程,分析总结了世界范围内开展的SCWO环境中设备腐蚀及监测技术等方面的研究动态,提出了我国SCWO技术研究的未来发展方向。 相似文献
204.
205.
为适应风险因素不确定性、随机性及动态反馈性等特点,建立新型富水岩溶隧道涌水风险评价体系,提出1种基于云模型的模糊综合评价方法.选取5个1级指标、29个2级指标构建评价指标体系;综合层次分析、熵权与加权平均计算法合理分配各指标权重;利用云生成算法计算出云数字特征参数并生成足够数量的云滴;将方法应用于贵州省某隧道涌水风险评... 相似文献
206.
在研究国内外利用雨水构建城市水环境的文献基础上,得出城市水环境构建要空中层、地表层和地下层综合构建三位一体的指导思想,以雨水为核心的城市水环境构建的思路是:从易到难,分步骤进行构建。 相似文献
207.
长江经济带是我国重要的战略区域,加强长江经济带生态环境保护是我国的重大战略部署,在推进我国"五位一体"总体布局建设中具有重要地位,是体现习近平总书记"共抓大保护,不搞大开发"的重要精髓。目前,总磷已成为长江经济带水体首要污染指标,总磷超Ⅲ类的断面比例达到18.3%,主要的一级支流中,沱江、清水江、岷江、乌江总磷平均浓度在地表水Ⅲ类水质标准上下浮动,污染相对较重;长江经济带总磷污染主要受工业、城镇生活、农业等污染源影响,主要涉及四川、贵州、湖北、湖南、重庆等地区;同时结合总磷污染特征分析,提出了涉磷工业企业治理、磷矿管理、城镇生活污水治理、畜禽养殖防治、规范监测方法等治理措施,为长江经济带总磷污染防控提供技术支撑和决策依据。 相似文献
208.
水质模型参数的确定是构建水质模型的基础。相对于传统优化方法,现代优化算法的优势日趋明显。本文在基于现代优化算法的水质模型参数确定研究背景下,介绍了具有代表性的遗传算法和模拟退火算法,并对该两种算法的应用现状进行综述,旨在推进该领域的进一步探索。 相似文献
209.
水资源的可持续开发与利用 总被引:1,自引:0,他引:1
水是一切生物生存环境的最重要支撑,只有可持续地开发利用水资源,才能创造一个可持续发展的社会和生存环境。针对日趋严重的淡水资源危机,本文以水资源的可持续存在为基础,从整体的角度出发,而不是就水论水,探讨了可持续开发、利用水资源的五个途径:经济向生态效益型转向、可持续开发水资源、建立水资源核算体系、建立水资源政策分析机制、人人参与水资源管理,从而实现环境完整性、经济效率和平衡三个基本目标。 相似文献
210.
针对农村生活污水污染问题已成为影响我国农村水环境的主要因素以及目前黑灰分离收集处理与现状不相符合,本文对崇明县某村的污水排放特征以及水量水质进行调研,并对硝化预处理系统结合人工湿地反硝化以及脱氮预处理结合人工湿地深度处理两种运行模式进行了深入探讨并分析了其去除机理,结果显示,硝化预处理系统结合人工湿地反硝化由于后续反硝化需要投加大量碳源从经济管理方面而言变得不可行;脱氮预处理结合人工湿地深度处理在预处理系统以进水3h、曝气2h、沉淀0.5h、排水0.5h、气水比40∶1的模式运行、人工湿地水力停留时间为48h条件下出水可满足《城镇污水处理厂污染物排放标准》(GB18918-2002)的二级要求,且因氨氮指标的降低大幅缩短了人工湿地的水力停留时间而减小占地面积。 相似文献