地下水开发引起的环境问题与治理

随着社会经济的飞速发展,人民生活对水资源的需求量日益增加,水资源开发已然成为备受社会各界关注的一项话题。而若是未能重视资源开发合理性与适宜性,必然会造成一定的环境污染。本文阐述了我国水资源开发与利用现状,分析了地下水开发引起的环境问题,并探究了新形势下治理地下水开发环境问题的有效对策。     

Catalytic oxidation of CO over Pt/Fe3O4 catalysts: Tuning O2 activation and CO adsorption

• Strong metal-support interaction exists on Pt/Fe₃O₄ catalysts. • Pt metal particles facilitate the formation of oxygen vacancies on Fe₃O₄. • Fe₃O₄ supports enhance the strength of CO adsorption on Pt metal particles. The self-inhibition behavior due to CO poisoning on Pt metal particles strongly impairs the performance of CO oxidation. It is an effective method to use reducible metal oxides for supporting Pt metal particles to avoid self-inhibition and to improve catalytic performance. In this work, we used in situ reductions of chloroplatinic acid on commercial Fe₃O₄ powder to prepare heterogeneous-structured Pt/Fe₃O₄ catalysts in the solution of ethylene glycol. The heterogeneous Pt/Fe₃O₄ catalysts achieved a better catalytic performance of CO oxidation compared with the Fe₃O₄ powder. The temperatures of 50% and 90% CO conversion were achieved above 260°C and 290°C at Pt/Fe₃O₄, respectively. However, they are accomplished on Fe₃O₄ at temperatures higher than 310°C. XRD, XPS, and H₂-TPR results confirmed that the metallic Pt atoms have a strong synergistic interaction with the Fe₃O₄ supports. TGA results and transient DRIFTS results proved that the Pt metal particles facilitate the release of lattice oxygen and the formation of oxygen vacancies on Fe₃O₄. The combined results of O₂-TPD and DRIFTS indicated that the activation step of oxygen molecules at surface oxygen vacancies could potentially be the rate-determining step of the catalytic CO oxidation at Pt/Fe₃O₄ catalysts. The reaction pathway involves a Pt-assisted Mars-van Krevelen (MvK) mechanism.     

In situ hydrothermal fabrication of visible light-driven g-C3N4/SrTiO3 composite for photocatalytic degradation of TC

Environmental Science and Pollution Research - A series of g-C3N4/SrTiO3 (CN/SrTiO3) composites with the different mass ratio of g-C3N4 were prepared by facile in situ hydrothermal growth method,...     

Effects of rainfall on surface environment and morphological characteristics in the Loess Plateau

Environmental Science and Pollution Research - Slope failure is a one of major process that causes severe landform variation and environment variation, and slope failure has become a major hidden...     

底泥性质对重金属生物淋滤效果的影响

生物淋滤技术是一项可以将重金属从污染底泥或土壤中分离出来的环境修复技术,具有反应温和、耗酸少、运行成本较低、去除效率高,以及脱毒后底泥的脱水性能好等优点。然而,底泥成分复杂、流域特异性高,这使得相似的生物淋滤工艺对不同底泥的重金属去除效果不尽相同、淋滤技术的工艺参数标准化难度增加。综述了底泥性质对淋滤反应的3方面影响:底泥中的有机质与酸可挥发性硫化物(AVS)会改变重金属的形态;pH、可还原性硫、水溶性有机物(DOM)会对淋滤功能菌的活性产生影响;底泥粒度和耗酸能力(ACC)也会影响重金属的化学淋出效果。在此基础上提出今后该技术有待开展的研究内容,以期为该技术的进一步推广应用提供理论依据和技术支撑。     

液膜分离技术处理含Cr6+废水的研究

采用液膜分离技术处理Cr^6＋质量浓度为200—1000mg／L的废水,考察了膜溶剂、载体、内水相、外水相、pH、乳水比（乳液与废水的体积比）等因素对处理效果的影响,通过正交实验得出最佳实验条件。结果表明,在膜溶剂为煤油、载体为三辛胺、内水相为氯氧化钠、氢氧化钠质量分数为2％、pn为1、乳水比为1：4的最佳条件下,Cr^6＋的去除率可达98．4％。     

城市环境地球化学调查研究方法综述

总结了城市环境地球化学调查的技术路线,论述了城市环境地球化学解释的思路和方法,提出了城市环境地球化学调查研究的重点问题及研究方向,为开展城市环境调查和评价工作提供了有参考价值的研究线索。     

填埋场沼气发电的温室气体减排效益分析

填埋场沼气是垃圾卫生填埋场产生的可利用资源.以深圳下坪垃圾填埋场为例,定量分析垃圾填埋气体发电的温室气体减排效益.结果表明,填埋场沼气发电具有很好的经济效益和环境效益,可作为与发达国家进行CDM(清洁发展机制)项目合作的优先技术领域.     

利用废渣盐石膏制作轻型墙体材料

研究利用海盐化工产生的废渣盐石膏经过一定工艺处理,生产轻型墙体材料盐石膏空心条板,该产品与天然石膏空心条板相比,原料采用及生产工艺都有较大改进,生产成本却大幅度下降。经测试,该产品完全可替代天然石膏空心条板,技术性能指标达到了国家规定的相关标准。     

Distance and flow effects on microsphere transport in a large gravel column

Consumption of microbially contaminated ground water can cause adverse health effects and the processes involved in pathogen transport in aquifers need to be understood. The influences of distance, flow velocity, and colloid size on colloid transport were examined in homogenous pea-gravel media using an 8-m column and three sizes (1, 5, and 10 microm) of microspheres. Experiments were conducted at three flow rates by simultaneously injecting microspheres with a conservative tracer, bromide. Observed concentrations were simulated with CXTFIT and analyzed with filtration theory. The results demonstrate that colloid concentration is strongly log-linearly related to transport distance (as suggested by filtration theory) in coarse gravels, similar to our previous field studies. In contrast, the log-linear relationship is often reported to be invalid in fine porous media. The observed log-linear relationship is possibly because straining is negligible in the coarse gravels investigated. This has implications in predicting setback distances for land disposal of effluent, and suggests that setback distances in gravel aquifers can be estimated using constant spatial removal rates (f). There was an inverse relationship between transport distance and colloidal concentration, but not with temporal attachment rate (katt) and collision coefficient (alpha). Increases in flow velocity result in increasing colloidal recovery, katt and alpha but decreasing f. Increases in sphere size result in decreasing colloidal recovery with increasing katt, f, alpha, and velocity enhancement. Diffusion is the dominant collision mechanism for 1-microm spheres (81-88%), while settling dominates for 5- and 10-microm spheres (> 87%), and interception is very small for all spheres investigated.