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渗滤液污染包气带中铁的形态变化 总被引:1,自引:0,他引:1
从渗滤液场龄和包气带岩性两方面出发,研究了新、老渗滤液对亚粘土和细砂包气带环境中Fe的含量及存在形态的影响。结果表明:新、老渗滤液分别能使细砂包气带介质中除残渣态以外Fe的含量增加16.68%或降低13.82%。亚粘土比细砂作为包气带介质更能缓冲渗滤液对介质中Fe的影响程度,其受影响范围在包气带0~20 cm深度处。当亚粘土为介质的包气带被新渗滤液污染后,其表层介质中碳酸盐结合态Fe的含量会增加15倍之多,为缓冲渗滤液Fe的污染做出了巨大贡献,但这部分Fe的存在也是潜在的二次污染源,在环境pH急剧变化的情况下,它可能会引起地下水高铁污染。 相似文献
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杭州市大气降尘重金属污染特征及来源研究 总被引:5,自引:0,他引:5
于2006年6月至2009年6月期间,在杭州市主城区7个采样点对大气降尘进行采集,并对10种重金属元素含量进行了分析。结果表明:重金属元素Cu、Cd、Mn、Ni、Pb、Zn、Co、Al、Fe、Mo质量浓度分别为223.6、15.6、741.1、27.8、363.7、1 820.4、7.0、8 982.4、21 149.0、13.4mg/kg;各功能区差异较大,半山(工业区)Fe、Mn、Pb、Zn浓度较高,江城立交(交通枢纽)Cu、Cd浓度较高。富集因子评价结果表明,Cd、Mo、Pb、Zn、Cu富集程度较高,受到不同程度人为污染。主因子分析结果显示,Mn、Fe可能来自钢铁冶炼及机械制造;Cu、Cd可能来自交通源;Zn、Mo可能来自相关的冶炼加工及合金工业;Ni、Co可能由煤和石油等化石燃料燃烧排放;Pb来自工业排放;Al主要来自地壳。 相似文献
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生活垃圾堆肥浸提液组成及其演化规律 总被引:2,自引:0,他引:2
堆肥浸提液与渗滤液组成相似,研究生活垃圾堆肥浸提液组成与演化特征可以为堆肥过程污染控制和堆肥质量改善提供科学依据。通过基本理化指标和三维荧光光谱分析,研究了生活垃圾堆肥浸提液的组成和转化特性。结果显示,在堆肥一次和二次发酵过程中,浸提液p H由5.43上升至9.24,无机阴离子无显著变化,电导率(EC)稳定在7.50m S/cm上下波动,ORP为正值,总氮从611.08 mg/L下降至177.43 mg/L,NH+4-N和NO-3-N浓度变化不明显,NO-2-N从未检出到后期达10.28 mg/L,有机氮从246.64 mg/L下降至172.52 mg/L。溶解性有有机物含量(DOC)从7 419.00 mg/L降至5 569.00 mg/L,其中的有机物发生降解和转化,生成胡敏酸和富里酸等物质。浸提液中重金属Fe、Cd、Cu、Zn、Cr、Mn、Ni和As浓度升高。通过研究发现,在堆肥中添加木屑等填料可以降低浸提液中NH+4-N的浓度,具有除臭作用,同时对p H值、EC和ORP均有调节作用,能提高堆肥的土地可利用性。 相似文献
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四川省某铅锌矿尾矿库周边环境重金属污染特征 总被引:1,自引:0,他引:1
《环境污染与防治》2016,(6)
对四川省某铅锌尾矿库周边土壤、地表水和地下水中的重金属含量及其相关性进行了研究。结果表明:(1)尾矿库周边土壤中Pb、Zn、Cd、As分别为19.8~187.0、11.6~249.0、0.01~3.44、2.6~9.3mg/kg。土壤中重金属元素都存在一定的相关性,Pb与Zn相关系数为0.951,达到极显著相关。(2)尾矿库周边土壤并未受到大面积的重金属污染,综合污染指数平均值为0.98,而选矿厂废水排放至尾矿库的明渠、尾矿库渗滤液排水沟附近土壤污染达到中污染水平。(3)尾矿库尾砂堆积处两翼地下水中有一定Pb污染,推断因为尾砂深度堆积与地下水直接接触。(4)含高浓度硫酸盐的尾矿库废水携重金属沿尾矿库重力坝下渗,对尾矿库渗滤液排放口下游区土壤、地下水造成了重金属和硫酸盐污染。 相似文献
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非正规垃圾填埋场已成为地下水的潜在污染源,给城市供水安全带来了极大风险。以北京某非正规垃圾填埋场的3种典型包气带介质为研究对象,以Br-为示踪剂,采取土柱实验和数值模拟相结合的方法,通过对场区3种典型包气带介质饱和与非饱和状态下的Br-迁移速率的比较,探讨包气带介质对污染物的阻滞能力。结果表明,Br-在不同包气带介质饱和状态下的迁移速率为中砂>细砂>砂质粉土,这可能与不同介质中粉粒和粘粒的含量有关,同时介质的有机质含量也会影响Br-的迁移速率,但前者因素占了主导作用;在Br-迁移过程中,不同包气带介质的含水量是影响其迁移速率的主要因素,若能合理控制场区的地下水位,使得包气带介质长期处于非饱和状态,将会大大延缓垃圾渗滤液中污染物向地下水迁移;针对特定的非正规垃圾填埋场,可采取抽水等措施,控制场区的细砂和砂质粉土层处于非饱和状态,充分利用包气带介质在非饱和状态时较强的污染物阻滞能力,阻隔或延缓垃圾渗滤液中的污染物进入地下水中。 相似文献
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针对硫酸盐还原菌(SRB)处理酸性矿山废水缺乏有效有机碳源问题,运用生活污水、鸡粪和锯末质量比80∶7∶3混合物的发酵液作为新型有机碳源驯化硫酸盐还原菌SRB,并研究SRB以该新型有机碳源作为营养物质在不同COD/SO2-4(C/S)值、pH值、初始硫酸根(SO2-4)浓度、重金属离子(Fe2+、Mn2+、Cu2+和Zn2+)浓度条件下对SO2-4的去除效果,以确定SRB去除SO2-4的最佳反应条件。实验结果表明,在厌氧环境SRB接种量8%、生长温度35℃、转速50 r/min、C/S为1.5~2.0、pH值6~7、初始SO2-4浓度≤3 000 mg/L、Fe2+在100~300 mg/L、Mn2+为35 mg/L时反应条件最佳,SO2-4去除率均可达90%以上;其中Fe2+浓度≤500 mg/L、Mn2+浓度≤140 mg/L时均会促进SRB对SO2-4的还原,当Fe2+浓度≥600mg/L时会严重抑制SRB,Mn2+浓度140 mg/L时会抑制SRB;Cu2+、Zn2+的存在对SRB均有影响,当Cu2+浓度15 mg/L时、Zn2+浓度45 mg/L时对SRB均有抑制作用。新型有机碳源可作为SRB的优良有机碳源,同时可实现以废治废的目的。该成果为实际应用提供了参考。 相似文献
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矿化垃圾和绿色植物废弃物对盐碱土的改良效果 总被引:2,自引:0,他引:2
利用矿化垃圾和绿色植物废弃物在上海临港新城进行盐碱土现场改良试验,并监测不同处理土壤溶液中重金属元素浓度.结果表明:(1)在盐碱土中分别加入矿化垃圾、绿色植物废弃物或2者混合加入能明显降低盐碱土的盐分,提高土壤的肥力,达到改良盐碱土的目的.(2)各处理土壤溶液中重金属变化趋势基本一致:Cu浓度低于<地下水质量标准>(GB/T 14848-93)中Ⅲ类标准,Cr浓度均在GB/T 14848-93中Ⅳ类标准内,不存在Cu和Cr污染可能;个别点土壤溶液中偶尔出现Zn和Pb浓度超过GB/T 14848-93中Ⅴ类标准,大部分基本在GB/T 14848-93中Ⅳ类标准内;Cd、Fe和Mn浓度相对较高,是造成地下水潜在污染的原因,要注意合理控制.(3)不同处理会影响矿化垃圾中重金属的溢出,会使一部分重金属向下迁移,但总体对地下水质影响不大,且100 cm处各种重金属元素的平均浓度均没有超过GB/T 14848-93中Ⅳ类标准.(4)矿化垃圾中加入绿色植物废弃物处理的污染综合指数较小,主要是由于绿色植物废弃物重金属元素浓度相对较低、有机质含量高,和矿化垃圾混合使用能降低矿化垃圾潜在污染的风险. 相似文献
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The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment. 相似文献
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A R Main 《Journal of environmental science and health. Part. B》1983,18(1):29-63
The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's. 相似文献
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Soudamini Mohapatra 《Journal of environmental science and health. Part. B》2013,48(7):513-520
The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg?1 and tebuconazole 0.673 and 1.95 mg kg?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues. 相似文献
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STEFANO POLATI FABIO GOSETTI VALENTINA GIANOTTI MARIA CARLA GENNARO 《Journal of environmental science and health. Part. B》2013,48(6):765-779
The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested. 相似文献
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Polati S Gosetti F Gianotti V Gennaro MC 《Journal of environmental science and health. Part. B》2006,41(6):765-779
The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested. 相似文献
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Singh Nishi Kumari Choudhary Sangeeta 《Environmental science and pollution research international》2021,28(42):58819-58836
Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining... 相似文献
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畜禽养殖业污染与循环经济 总被引:16,自引:0,他引:16
解决畜禽养殖业的污染问题要以充分利用资源为根本出发点,通过对污染全过程控制及废物综合利用,达到畜禽粪便的减量化、无害化、资源化,走循环经济的发展道路。 相似文献
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The degradation and ecotoxicity of sulfonylurea herbicide rimsulfuron and its major metabolites were examined in batch samples of an alluvial sandy loam and in freshwater. An HPLC-DAD method was adapted to simultaneously identify and quantify rimsulfuron and its metabolites, which was successfully validated by GC-MS analysis. In aqueous solutions, pure rimsulfuron was rapidly hydrolyzed into metabolite 1 (N-(4,6-dimethoxypyrimidin-2-yl)-N-(3-(ethylsulfonyl)-2-pyridinylurea)), which itself was transformed into the more stable metabolite 2 (N-((3-(ethylsulfonyl)-2-pyridinyl)-4,6-dimethoxy-2-pyrimidineamine)), with half-life (t(1/2)) values of 2 and 2.5 days, respectively. Hydrolysis was instantaneous under alkaline conditions (pH = 10). In aqueous suspensions of the alluvial soil (pH = 8), formulated rimsulfuron had a half-life of 7 days, whereas that of metabolite 1 was similar to that in water (about 3.5 days). The degradation of the two major metabolites was also studied in soil suspensions with the pure compounds at concentrations ranging from 1 to 10 mg l(-1). The half-life of metabolite 1 ranged from 3.9 to 5 days, close to the previous values. Metabolite 2 was more persistent and its degradation is strongly dependent on the initial concentration (C0): half-life values ranged from 8.1 to 55 days at 2-10 mg l(-1), respectively. These values are higher than those determined from the kinetics of metabolite 1 transformation into metabolite 2 (t(1/2) = 8-19 days). The ecotoxicity of the three chemicals was evaluated through their effect on Daphnia magna and Vibrio fischeri (Microtox bioassay). No effect was observed on D. magna with 24 and 48 h acute toxicity tests. Similarly, no toxic effect was observed with the Microtox test for the three chemicals in the range of concentrations tested that included the field application dose. Thus, being of low persistence and lacking acute toxicity, these chemicals present a low environmental risk. However, chronic effects should be studied in order to confirm the safety of rimsulfuron and its major metabolites. 相似文献
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《Atmospheric environment (Oxford, England : 1994)》2007,41(37):8228-8240
Isocyanatocyclohexane and isothiocyanatocyclohexane are becoming relevant compounds in urban and industrial air, as they are used in important amounts in automobile industry and building insulation, as well as in the manufacture of foams, rubber, paints and varnishes. Glass multi-sorbent tubes (Carbotrap, Carbopack, Carboxen) were connected to LCMA-UPC pump samplers for the retention of iso- and isothiocyanatocyclohexanes. The analysis was performed by automatic thermal desorption (ATD) coupled with capillary gas chromatography (GC)/mass spectrometry detector (MSD). TD-GC/MS was chosen as analytical method due to its versatility and the possibility of analysis of a wide range of volatility and polarity VOC in air samples. The method was satisfactory sensitive, selective and reproducible for the studied compounds. The concentrations of iso- and isothioisocyanatocyclohexanes were evaluated in different urban, residential and industrial locations from extensive VOC air quality and odour episode studies in several cities in the Northeastern edge of Spain. Around 200–300 VOC were determined qualitatively in each sample. Higher values of iso- and isothiocyanatocyclohexane were found in industrial areas than in urban or residential locations. The concentrations ranged between n.d.−246 and n.d.−29 μg m−3 for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively, for industrial areas. On the other hand, urban and residential locations showed concentrations ranging between n.d.−164 and n.d.−29 μg m−3 for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively. The site location (urban or industrial), the kind and nearness of possible iso- and isothiocyanatocyclohexane emission activities (industrial or building construction) and the changes of wind regimes throughout the year have been found the most important factors influencing the concentrations of these compounds in the different places. 相似文献