Assessing field vulnerability to phosphorus loss in Beijing agricultural area using Revised Field Phosphorus Ranking Scheme

Guanting Reservoir,one of the drinking water supply sources of Beijing,suffers from water eutrophication.It is mainly supplied by Guishui River.Thus,to investigate the reasons of phosphorus(P)loss and improve the P management strategies in Guishui River watershed are important for the safety of drinking water in this region.In this study,a Revised Field P Ranking Scheme(PRS)was developed to reflect the field vulnerability of P loss at the field scale based on the Field PRS.In this new scheme,six factors are included, and each one was assigned a relative weight and a determination method.The affecting factors were classified into transport factors and source factors,and,the standards of environmental quality on surface water and soil erosion classification and degradation of the China were used in this scheme.By the new scheme,thirty-four fields in the Guishui River were categorized as"low","medium"or"high"potential for P loss into the runoff.The results showed that the P loss risks of orchard and vegetable fields were higher than that of corn and soybean fields.The source factors were the main factors to affect P loss from the study area.In the study area,controlling P input and improving P usage efficiency are critical to decrease P loss.Based on the results,it was suggested that more attention should be paid on the fields of vegetable and orchard since they have extremely high usage rate of P and high soil test of E Compared with P surplus by field measurements,the Revised Field PRS was more suitable for reflecting the characteristics of fields,and had higher potential capacity to identify critical source areas of P loss than PRS.     

气体脱硫胺液系统的清洁生产

分析了气体脱硫装置胺液系统污染物的主要来源和危害,通过采取清洁生产工艺、材质升级、在线净化复活、停工清扫塔器和新脱硫剂补充置换等措施,取得了较好的效果.     

矿区可持续发展能力建设中生态环境管理研究

实现矿区的可持续发展有赖于发展模式的转变,转变传统的生态环境管理的基本观念,提出要完善和优化矿区的生态环境管理体制,建立矿区"环境-资源-经济"信息管理系统和生态环境综合分析决策模型,寓经济发展于环境管理中,寓环境管理建设于经济发展中,寓矿区发展于环境和经济的协调发展之中,推进矿区持续发展,为矿区环境保护和经济发展建立一个和谐的可持续发展模式.     

黑藻吸附Cu2+机制研究

生物吸附法是一种经济有效的去除废水中有害重金属离子的方法.以黑藻(Hydrilla verticillata)干样为生物吸附材料,研究了黑藻对水体中Cu<'2+>等温吸附的基本特征,并通过测定吸附前后溶液离子浓度变化以及pH值、基团屏蔽对Cu<'2+>吸附的影响,结合红外光谱技术,从静电吸附作用、离子交换作用、基团作用...     

辅料配比对污泥生物-物理联合干燥的影响

利用自主研制的污泥生物-物理联合干燥反应系统研究了脱水污泥∶树皮∶回流污泥分别为7∶3∶0.5、9∶3∶0.5和12∶3∶0.5时,污泥生物-物理联合干燥过程中温度、含水率等参数的变化规律.结果表明,污泥温度随干燥时间延长先增大后减小,含水率在0～96 h逐渐降低,继续延长反应时间,则变化不明显.当脱水污泥∶树皮∶回流...     

Mn对超富集植物短毛蓼和水蓼生长、Mn吸收及氮素代谢的影响

采用水培的方法,研究了不同浓度Mn(0.0003、0.5、1、2、4、8 mmol · L^-1)对Mn超富集植物短毛蓼(Polygonum pubescens Blume)和水蓼(Polygonum hydropiper L.)叶片铵态氮、硝态氮、游离脯氨酸、可溶性蛋白质含量及氮素代谢关键酶:硝酸还原酶(NR)、谷氨酰胺合成酶(GS)、谷氨酸合酶(GOGAT)和谷氨酸脱氢酶(GDH)活性的影响.结果表明,随着Mn处理浓度的增加,短毛蓼和水蓼的根、茎、叶中Mn含量显著增加(p<0.05),在相同Mn处理浓度下短毛蓼中Mn含量均大于同部位水蓼中Mn含量.在Mn处理浓度小于1 mmol · L^-1时,Mn对短毛蓼的株高、株重影响不显著,但对水蓼的影响显著(p<0.05),表明短毛蓼比水蓼更耐Mn污染.Mn处理显著降低了短毛蓼硝态氮含量(p<0.05),提高了可溶性蛋白质含量,浓度为8 mmol · L^-1的Mn处理显著提高了水蓼硝态氮、铵态氮、可溶性蛋白质含量及短毛蓼、水蓼游离脯氨酸含量(p<0.05).Mn引起了短毛蓼和水蓼氮素代谢关键酶活性的变化,显著降低了水蓼叶片NR、短毛蓼叶片GS活性(p<0.05);在Mn处理浓度为1 mmol · L^-1时,短毛蓼叶片NR活性最高,为对照的1.91倍,而2、4、8 mmol · L^-1 Mn处理显著降低了短毛蓼和水蓼GOGAT活性(p<0.05).另外,Mn处理显著提高了短毛蓼和水蓼叶片GDH活性(p<0.05),在Mn处理浓度为8 mmol · L^-1时,短毛蓼、水蓼叶片GDH活性分别为对照的16.29倍和1.29倍.     

含油污泥无害化处置优化研究及生命周期评价

提出含油污泥的优化处置方案,并通过生命周期评价方法(LCA)对优化方案进行环境影响评价。结果表明,与原处置工艺相比优化后环境负荷降低了99.62%。     

一体化接触氧化反应器处理景区生活污水

常州某旅游景区采用一体化生活污水处理装置处理该区生活污水,通过试验确定反应器的最佳工艺参数,研究表明采用接触氧化反应器处理农村污水,在反应器内溶解氧维持在2.0~4.0 mg/L,水力负荷为3.53 m3/(m3.d)的运行条件下,对COD、NH3-N及TN去除率分别达80.82%、69.12%、63.16%,出水可稳定达GB18918-2002《城镇污水处理厂污染物排放标准》一级标准。     

Transport and fate of mercury under different hydrologic regimes in polluted stream in mining area

Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4 2??) were lower during higher flow due to dilution. Due to both sedimentation of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within 10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60% for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction (DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved phase in surface waters in Wanshan (over 95%).     

Chemical cleaning of fouled PVC membrane during ultrafiltration of algal-rich water

Cleaning of hollow-fibre polyvinyl chloride (PVC) membrane with di erent chemical reagents after ultrafiltration of algal-rich water was investigated. Among the tested cleaning reagents (NaOH, HCl, EDTA, and NaClO), 100 mg/L NaClO exhibited the best performance (88.4% 1.1%) in removing the irreversible fouling resistance. This might be attributed to the fact that NaClO could eliminate almost all the major foulants such as carbohydrate-like and protein-like materials on the membrane surface, as confirmed by Fourier transform infrared spectroscopy analysis. However, negligible irreversible resistance (1.5% 1.0%) was obtained when the membrane was cleaning by 500 mg/L NaOH for 1.0 hr, although the NaOH solution could also desorb a portion of the major foulants from the fouled PVC membrane. Scanning electronic microscopy and atomic force microscopy analyses demonstrated that 500 mg/L NaOH could change the structure of the residual foulants on the membrane, making them more tightly attached to the membrane surface. This phenomenon might be responsible for the negligible membrane permeability restoration after NaOH cleaning. On the other hand, the microscopic analyses reflected that NaClO could e ectively remove the foulants accumulated on the membrane surface.