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潜流人工湿地污染河水处理系统中的填料堵塞问题研究 总被引:1,自引:1,他引:1
利用潜流人工湿地系统处理污染河水,水力负荷为0.15 m3/(m2·d).研究了该系统长期运行过程中的填料堵塞问题及其对污染物去除率的影响.构建了潜流人工湿地污染河水处理中试系统,在运行两年后,潜流人工湿地填料存在一定的堵塞现象,填料孔隙率最大减少了2.67%.填料孔隙堵塞现象主要发生在该中试系统的前段(沿水流方向距进水点0~5 m),其填料堵塞物质主要为无机颗粒物.植物对填料堵塞问题的改善作用并不显著.填料的部分堵塞对该中试系统中污染物的去除率有一定的影响,运行第2年氨氮的去除率略有降低,而COD的去除率有增加的趋势. 相似文献
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构建小试试验研究了正反粒径混合级配填铺与正粒径级配填铺(组合填料为钢渣与灰岩)的垂直潜流人工湿地单元对生活污水中各主要指标的降解效果,同时比较分析了填料填铺方式对缓解人工湿地堵塞问题的影响.结果表明,当原水COD在134.72~653.33 mg/L、NH3-N在42.72~272.60mg/L,TN在107.40~6... 相似文献
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针对人工湿地内部DO含量较低引起的生物性堵塞,污水处理效率下降的问题,采用投加释氧材料的方法来提高湿地内部DO含量,修复生物性堵塞。采用CaO_2为释氧剂制备释氧材料,进行释氧性能研究。结果表明:采用大孔弱酸性丙烯酸系阳离子交换树脂作为包埋剂制成的释氧材料释氧性能最佳。在模拟人工湿地污水系统中,释氧材料可使反应器中DO质量浓度在15d内保持在5.0mg/L以上,并且pH保持中性水平,相较未投加释氧材料的对照组,30d内COD的平均降解效率提高125%。投加释氧材料可以使发生生物性堵塞的人工湿地系统在连续运行条件下基质孔隙率在15d内恢复到初始水平的83%左右,并且相较机械曝气具有操作便捷、不受环境限制以及成本低廉的优点。 相似文献
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《环境工程学报》2016,(6)
选择石砾、粗砂、细砂作为垂直流人工湿地的基质在实验室内研究不同粒径的基质在不同的水力负荷和对不同浓度污水对污染物的去除效果,根据实验结果选取基质应用于示范基地,利用人工湿地模型Subwet2.0对人工湿地示范基地进行模型模拟,为农村生活污水人工湿地系统的处理设计及模拟出水水质提供参考。研究结果表明:石砾、粗砂、细砂为基质对污染物去除率较好的水力负荷分别为小于0.9、0.6和0.3 m/d时;石砾基质对COD的最佳污染负荷为970 mg/L,粗砂、细砂基质为468~970 mg/L;粗砂和细砂基质对NH_4~+-N去除效果相似;在北方地区垂直流人工湿地主体基质建议使用粗砂或石砾以减少堵塞的风险;利用Subwet2.0模型模拟人工湿地示范基地的出水水质,根据当地条件在反应参数的取值范围内调整了相应的参数值,模拟的结果符合性很高。 相似文献
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人工湿地处理城市污水效能的影响因素分析 总被引:2,自引:0,他引:2
为解决人工湿地占地面积大、处理效率低、容易堵塞,往往需要间歇运行等问题,通过对传统的人工湿地进行改造,设计一套新型人工湿地床系统——折流式湿地床 侧流式湿地床,并通过试验对其处理城市污水的运行效能的影响因素进行了研究.研究结果表明,降雨、蒸腾和蒸发、温度、植物收割及堵塞作用对人工湿地运行有不同程度的影响,人工湿地受降雨因素的影响,其出水COD值比降雨前低,同时较人工湿地由于降雨作用所导致的COD稀释浓度高2.4~5.7 mg/L,而降雨使出水SS比降雨前高5.0~7.2 mg/L;堵塞缩短了折流湿地床的运行周期及降低了COD的去除,水力负荷为102.87 cm/d时,运行周期为20 d,水头损失由5.2 cm增至14.8 cm,COD去除率由84.35%降至21.19%;水力负荷为137.16 cm/d时,运行周期为16 d,水头损失由5.0 cm增至15.0 cm,COD去除率由81.26%降至7.35%. 相似文献
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人工湿地数学模型模拟与应用 总被引:1,自引:0,他引:1
人工湿地生态系统具有投资低、出水水质好、抗冲击力强、增加绿地面积和操作简单等优点,在国外得到了较好应用.综述了人工湿地净化技术及湿地模型的研究进展,重点介绍了国外已经成功验证与应用的3种人工湿地模型的开发情况.同时应用某人工湿地的实测数据,通过对模型的验证和率定,表明模型在评估湿地功能和优化设计上的实用性.最后,对人工湿地模拟模型的应用前景及存在问题进行了评述. 相似文献
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选取金华、衢州、温州、丽水、宁波、杭州6个城市开展PM2.5手工标准方法和自动监测法比对实验,并用相关性和相对偏差两个指标对比对结果进行分析和评价。结果表明:(1)2013年6个采样城市采集的PM2.5手工和自动监测值均具有较好的相关性(相关系数均在0.95以上),截距均在-0.010~0.010mg/m3,但斜率相差较大(衢州和丽水在0.90以上;金华、温州和杭州在0.85~0.90;宁波在0.80以下)。(2)2013年6个城市采集的PM2.5手工和自动监测值的相对偏差为-34.2%~36.5%;PM2.5手工和自动监测值相对偏差在±15%范围内的数据占总数据量的82.6%;负偏差数据占总数据量的80.0%。(3)PM2.5手工标准方法和自动监测法的比对差异与地域、季节和PM2.5浓度等条件有关。总体上,不同地区PM2.5手工与自动监测值相对偏差绝对值(︱RD︱)年平均值为衢州丽水金华宁波温州杭州;春季PM2.5手工与自动监测值︱RD︱平均值高于夏季,秋季高于冬季;各采样城市PM2.5手工和自动监测值︱RD︱平均值在高质量浓度(PM2.5手工监测值(ρ1)0.150mg/m3)下最小,中质量浓度(0.050≤ρ1≤0.150mg/m3)下最大,低质量浓度(ρ10.050mg/m3)下介于两者之间。 相似文献
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Grahovac ZM Mitić SS Pecev ET Pavlović AN 《Journal of environmental science and health. Part. B》2010,45(8):783-789
In the present study, a new sensitive and simple kinetic-spectrophotometric method for the determination of the insecticide diflubenzuron [1-(4-chlorophenyl)-3-(2,6-diflubenzoil)urea] is proposed. The method is based on the inhibited effect of diflubenzuron on the oxidation of sulphanilic acid (SA) by hydrogen peroxide in phosphate buffer in presence Cu(II) ion. Diflubenzuron was determined with linear calibration graph in the interval from 0.31 to 3.1 μg mL?1 and from 3.1 to 31.0 μg mL?1. The optimized conditions yielded a theoretical detection limit of 0.18 μg mL?1 corresponding to 0.036 mg kg(-1)mushroom sample based on the 3S(b) criterion. The RSD is 5.03-1.83 % and 2.81-0.71 % for the concentration interval of diflubenzuron 0.31-3.1 μg mL?1 and 3.1-31.0 μg mL?1, respectively. The reaction was followed spectrophotometrically at 370 nm. The kinetic parameters of the reaction are reported, and the rate equations are suggested. The developed procedure was successfully applied to the rapid determination of diflubenzuron in spiked mushroom samples of different mushroom species. The HPLC method was used like a comparative method to verify results. 相似文献
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Z. M. Grahovac S. S. Mitić E. T. Pecev A. N. Pavlović 《Journal of environmental science and health. Part. B》2013,48(8):783-789
In the present study, a new sensitive and simple kinetic-spectrophotometric method for the determination of the insecticide diflubenzuron [1-(4-chlorophenyl)-3-(2,6-diflubenzoil)urea] is proposed. The method is based on the inhibited effect of diflubenzuron on the oxidation of sulphanilic acid (SA) by hydrogen peroxide in phosphate buffer in presence Cu(II) ion. Diflubenzuron was determined with linear calibration graph in the interval from 0.31 to 3.1 μg mL?1 and from 3.1 to 31.0 μg mL?1. The optimized conditions yielded a theoretical detection limit of 0.18 μg mL?1corresponding to 0.036 mg Kg?1mushroom sample based on the 3Sb criterion. The RSD is 5.03–1.83 % and 2.81–0.71 % for the concentration interval of diflubenzuron 0.31–3.1 μg mL?1and 3.1–31.0 μg mL?1, respectively. The reaction was followed spectrophotometrically at 370 nm. The kinetic parameters of the reaction are reported, and the rate equations are suggested. The developed procedure was successfully applied to the rapid determination of diflubenzuron in spiked mushroom samples of different mushroom species. The HPLC method was used like a comparative method to verify results. 相似文献
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农药废水是一种典型的高浓度有机工业废水 ,有机污染物浓度高 (CODCr>10 0 0 0mg L) ,可生化性差 (氯苯农药废水BOD5 CODCr=0 .0 3 ,对邻硝基氯苯农药废水BOD5 CODCr=0 .0 5 )。采用微电解和Fenton试剂氧化两种物化手段对菊酯、氯苯和对邻硝氯苯 3种废水按比例配制而成的综合农药废水进行预处理 ,结果表明 :在废水pH为 2— 2 .5时 ,经微电解处理后 ,BOD5 CODCr比值在 0 .45以上 ,可生化性提高 ;Fenton试剂对综合农药废水CODCr去除率为 60 %左右 ,色度去除率接近 10 0 % 相似文献
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A sensitive and reliable quantification method for Bisphenol A based on modified competitive ELISA method 总被引:1,自引:0,他引:1
Kim A Li CR Jin CF Lee KW Lee SH Shon KJ Park NG Kim DK Kang SW Shim YB Park JS 《Chemosphere》2007,68(7):1204-1209
Bisphenol A (BPA), generally known as bisphenols, has been identified as a potential estrogenic substance. BPA must be conjugated to carrier protein and BSA was commonly used. 4,4-Bis(4-hydroxyphenyl) valeric acid (BHPVA) has a bisphenolic structure and a long carbon chain with a reactive carboxyl group on the end. In this study, BHPVA-BSA was used to produce polyclonal antibody against bisphenolic structure, and a modified competitive ELISA method for quantification of BPA was developed. This system was based on BHPVA-BSA for polyclonal antibody production against bisphenolic structure, and BHPVA-HRP for determination of BPA substituting detection antibody in competitive reaction. Recovery was assessed at 10 different concentrations (2-1000 ng/ml) of BHPVA, and the recovery range was from 96.3% to 107.2%. The variation was from 6.2% to 9.8% for intra assay and from 10.1% to 12.6% for inter assay. The quadratic was used to establish the curve regression. The range was found to be between 2 and 1000 ng/ml. This modified competitive ELISA method has proven to be a very useful tool for quantification of BPA without the unexpected interaction of BSA and anti-BSA polyclonal antibody. 相似文献
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概述了竖向隔板分油法、蜂窝斜管分油法及磁性颗粒吸附过滤法 ,将这 3种方法结合处理某机修厂的含油污水 ,取得了满意效果。 相似文献