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1.
化学沉淀法去除垃圾渗滤液中氨氮的试验研究   总被引:10,自引:0,他引:10  
采用MgCl2·6H2O和Na2HPO4·12H2O或MgSO4和Na2HPO4·12H2O使NH3-N生成磷酸铵镁的化学沉淀法,考察了pH值,反应时间,药剂选用,药剂配比以及分步沉淀工艺等对垃圾渗滤液中氨氮去除率的影响.结果表明:在pH值为9.0,反应时间为25min,采用分步沉淀工艺,当药剂配比为:n(N):n(Mg):n(P)=1.5:1:1.5时,垃圾渗滤液中NH3-N, 沉淀降低到28.54 mg·l-1,去除率达98.10%.  相似文献   

2.
以复极性固定床电解槽为反应器,利用CuO-CeO2/γ-Al2O3多相催化剂取代传统反应器的绝缘填料,构建电-多相催化氧化耦合体系.考察了槽电压、pH值、气体流量和极间距等因素对渗滤液氨氮的影响.结果表明,当槽电压为15.0V,pH为7,曝气量为0.08m3·h-1,极板间距为3.0cm时,反应180min后,氨氮的去除率能达到94.7%.与传统石英砂相比较,利用CuO-CeO2/γ-Al2O3做绝缘填料,氨氮的处理效果明显提高.  相似文献   

3.
垃圾渗滤液中有机组分在混凝前后的变化   总被引:1,自引:1,他引:0  
垃圾渗滤液是生活垃圾填埋场主要的二次污染物,其成分非常复杂,目前还不能对渗滤液中的有机物进行全面分析.研究表明,经生物处理后的渗滤液中的主体有机物是腐殖酸.腐殖酸经过前处理工艺后仍有很多不可降解,因此,它是渗滤液中最主要的长期性有机污染物,是使渗滤液不能达到排放标准的主要问题.  相似文献   

4.
采用上流式厌氧污泥床处理某垃圾填埋场渗滤液.实验结果表明,在厌氧氨氧化活性稳定后,反应器对氨氮、亚硝氮具有较好的处理效果,氨氮和亚硝氮的平均去除率分别达到98.42%和99.01%,相应的平均容积去除负荷分别为93.64 mg·l-1·d-1和127.57 mg·l-1·d-1,COD的平均去除率为23.51%,平均容积去除负荷为84.53 mg·l-1·d-1.通过GC-MS总共检测出48种主要有机污染物,其中14种有机物的去除率为100%,2种有机物的去除率介于90%和100%之间,7种有机物的去除率介于50%和90%之间,此外还有13种有机物去除率低于50%,反应中亚硝氮和氨氮的去除率比值为1.37,反应器中存在厌氧氨氧化和反硝化的协同作用.  相似文献   

5.
垃圾填埋场渗滤液地下原位脱氮技术综述   总被引:1,自引:0,他引:1  
丁爱中  张慧  李宗良 《生态环境》2007,16(6):1814-1818
氨氮是城市垃圾厌氧填埋过程中产生的常见的污染物。由于氨氮的持久性和生物毒性,生活垃圾填埋场渗滤液中氮的脱除已引起了人们的高度关注。文中结合国内外的研究现状的基础,论述了厌氧渗滤液回灌、强制通风好氧填埋、准好氧填埋和生物反应器填埋四种垃圾渗滤液原位脱氮处理技术的原理、技术特点、工程投资、运行成本以及处理效果等;指出了垃圾填埋场渗滤液原位脱氮技术的未来研究重点:填埋场内脱氮机理和脱氮速率的深入研究、工艺控制优化研究以及生物反应器填埋的实际应用设计研究。  相似文献   

6.
纳米银(AgNPs)作为消费品中最常用的人工纳米材料,由于其优异的抗菌性能,在织物、医疗设备和食品及饮料包装中广泛使用.AgNPs可通过大气沉降、地表水径流、污水灌溉和生物污泥的土地施用等多种途径进入土壤等多孔介质,甚至进入地下水.AgNPs进入环境后可在动物和植物体内累积并产生毒性效应,对生态环境构成危害.因此,全面了解AgNPs在土壤等多孔介质中的迁移过程对正确评估其环境归趋和生态效应具有重要的理论和现实意义.本文针对近年来已发表的不同表面稳定剂、环境有机质、土壤矿物及微生物等对AgNPs性质及在多孔介质中迁移过程中产生的影响进行了全面的总结,并就目前研究中存在的问题和后续研究的发展方向进行了展望.  相似文献   

7.
受垃圾渗滤液影响,垃圾场周边土壤有机物含量增加。试验结果显示,随着土壤有机物含量的增加,土壤中有效态铁锰含量增大。垃圾场周边土壤中渗滤液有机物和金属铁锰共存时,大量的有机物质能活化土壤中的铁锰,增加其有效性,增强其在土壤中的迁移能力。从而造成垃圾场地下水较严重的铁锰污染。  相似文献   

8.
垃圾渗滤液中污染物在包气带运移模拟实验及预测   总被引:4,自引:0,他引:4  
为揭示垃圾渗滤液中污染物在包气带中的迁移转化规律,通过静态吸附、静态降解、动态土柱和数学模型预测等方法进行模拟实验。结果表明,包气带对污染物的吸附过程是线性的,即S=KdC,吸附系数Kd=0.0976;降解曲线符合一级动力学方程,即C=C0e-λt,降解系数λ=0.0324d-1;弥散过程符合对流-弥散迁移转化模型,弥散系数D=0.00435m2·d-1,由此确定了污染物迁移数学模型。通过动态土柱实验验证了模型的可靠性,并利用模型对垃圾渗滤液中有机污染物(COD)的时空分布进行预测。  相似文献   

9.
催化臭氧氧化去除垃圾渗滤液中难降解有机物的研究   总被引:6,自引:0,他引:6  
刘卫华  季民  张昕  杨洁 《环境化学》2007,26(1):58-61
研究了Fe(Ⅱ),Mn(Ⅱ),Cu(Ⅱ)作用下,均相催化臭氧氧化去除垃圾渗滤液中高浓度的腐殖质.分析催化剂用量、溶液pH值对腐殖质催化臭氧氧化降解的影响.结果表明,与单纯臭氧氧化比较,催化臭氧氧化对UV254和色度去除率无明显改善,但可明显提高以TOC和CODCr表征的有机物去除率;当投加催化剂过量时,以TOC和CODCr表征的有机物去除率虽降低,但仍有促进作用.但Fe2 的过量投加将明显抑制UV254和色度的去除效果.在碱性条件下,催化臭氧氧化法具有更好的去除效果.三种催化剂催化效果为Cu(Ⅱ)>Mn(Ⅱ)>Fe(Ⅱ).采用Cu(Ⅱ)催化臭氧氧化处理实际渗滤液生化处理出水,对CODCr,色度和UV254都显示出较好的去除效果.  相似文献   

10.
采用平衡解吸法研究了风沙土不同有机组分对氨氮的解吸特征影响。结果表明,去除腐殖质后的风沙土氨氮解吸比例增加(由0.58增加到0.68),同时,解吸迟滞性指数显著降低(由0.067降低到0.021),说明腐殖质是影响风沙土氨氮解吸特征的重要因素;氨氮在轻组有机组分上的表面分配作用吸附是导致解吸比例增大,解吸迟滞性指数减小的原因;重组有机组分中的紧结态腐殖质(胡敏素)对氨氮的解吸起关键作用,它不但解吸比例较低(Dr=0.23),而且解吸迟滞性指数较大(TⅡ=0.458);氨氮在紧结态和稳结态腐殖质所形成的团聚体颗粒微孔隙中的不可逆吸附是导致解吸比例降低、解吸迟滞性指数增大的根本原因;考查土壤对氨氮的解吸特征不但要考虑有机质的含量,更要考虑有机质的存在形态,它也是影响土壤氨氮解吸特征的重要因素,轻组有机组分、重组有机组分及重组有机组分中的稳结态加紧结态腐殖质(HⅡ+HⅢ组)和紧结态腐殖质(HⅢ组)携载的吸附态氨氮进入水体后,对上覆水体的扩散通量可分别按其饱和吸附量的0.94、0.58、0.33和0.23倍估算。  相似文献   

11.
Transport of engineered antibiotic resistance plasmids in porous media has been reported to potentially cause significant spreading of antibiotic resistance in the environment. In this work, transport of an indigenous resistance plasmid pK5 in porous media was investigated through packed column experiments. At identical ionic strengths in CaCl2 solutions, the breakthroughs of pK5 from soil columns were very close to those from quartz sand columns, indicating that transport of pK5 in quartz sand and soil was similar. A similarity in transport behavior was also found between pK5 and an engineered plasmid pBR322 that has approximately the same number of base pairs as pK5. The influence of surfactants, a major group of constituents in soil solutions, was examined using an engineered plasmid pcDNA3.1(+)/myc-His A. The impact of an anionic surfactant, sodium dodecyl sulfate (SDS), was negligible at concentrations up to 200 mg·L–1. Cetyltrimethyl ammonium bromide (CTAB), a cationic surfactant, was found to significantly enhance plasmid adsorption at high concentrations. However, at environmentally relevant concentrations (<1 mg·L–1), the effect of this surfactant was also minimal. The negligible impact of surfactants and the similarity between the transport of engineered and indigenous plasmids indicate that under environmentally relevant conditions, indigenous plasmids in soil also have the potential to transport over long distances and lead to the spreading of antibiotic resistance.
  相似文献   

12.
This study conducted in monitoring respirometer oxygen consumption of aerobic microorganism during biodegradation processes of ozonated organic matters, which can estimate both biodegraded efficiency and coefficient of natural organic matters (NOMs) in water source. It can be proposed that different ozone dosage might change biodegradation characteristics of organic matters. The result reveals that higher ozone dosage may cause higher biomass yield coefficient of microorganism, and cultured microorganism may easily utilize biodegradation organic matters (BOMs) produced by ozonation, finally increasing overall removal efficiency. Therefore, using respirometer to evaluate the production of BOMs by ozonation before the biological treatment is effective for controling ozone dosage and enhancement of NOMs removal by biological processes.  相似文献   

13.
焦化废水中溶解性有机物组分的特征分析   总被引:3,自引:0,他引:3  
焦化废水是典型的具有复杂有机质的工业废水,其复杂的有机构成制约了水处理的水质达标,且可能对排入水体构成危害.为了探明其溶解性有机物的组成,采用XAD-8大孔树脂将焦化废水中的溶解性有机物分为亲水性组分(HIS)、疏水酸性组分(HOA)、疏水碱性组分(HOB)和疏水中性组分(HON),分析了各组分的溶解性有机物(DOC)、紫外-可见光谱、色度,并采用GC/MS对各组分中有机物进行定性分析.结果表明,焦化废水中的有机物主要为HIS和HOA组分,其DOC含量分别占总DOC的44.3%和32.4%;焦化废水在200—250 nm和300—400 nm范围内有特征吸收峰,且吸收光强度顺序为HIS>HOA>HON>HOB;焦化废水的色度主要由HOA和HON构成,其在525 nm和436 nm处的吸光度分别占焦化废水吸光度的42.9%(HON)、42.1%(HON)和21.4%(HOA)、15.8%(HOA);焦化废水中亲水性物质主要是苯胺、苯酚、喹啉、异喹啉,疏水酸性物质中主要是各种甲基取代的酚类物质,疏水碱性物质主要是各种胺类和含氮杂环化合物,疏水中性物质主要是吲哚及其衍生物.  相似文献   

14.
Advanced oxidation processes based on sulfate radicals (SO 4 ·? ) are capable of efficiently degrade organic pollutants from ground, surface and wastewaters. However, this degradation may be limited by aqueous natural organic matter (NOM). Here we measured the absolute rate constants of reaction of SO 4 ·? with four types of organic matter: two fulvic acids and two lake organic matter. We used laser flash photolysis technique to monitor the SO 4 ·? decay and the formation of the transients from organic matters. Reaction rate constants comprised between 1530 and 3500 s?1 mgC?1 L were obtained by numerical analysis of differential equations and the weighted average of the extinction coefficient of the generated organic matters radicals between 400 and 800 M?1 cm?1.  相似文献   

15.
Nanoparticles are not specifically targeted in conventional treatment schemes; consequently, typical wastewater treatment systems are ineffective for nanoparticles removal. With rapidly increasing concern over their health effects, improved understanding of nanoparticle transport and retention in porous media filters is critical because of its application in new wastewater treatment methods and for assessment of the fate of the discharged nanoparticles in soil. In this study, a unique and robust integrated method is developed and validated. Experimentally, this approach uses an on-line, real-time, and in situ method for measuring nanoparticle retention dynamics, eliminating the laborious and less accurate sampling and off-line analysis. The data analysis part is a process simulator which provides both kinetic properties of the retention process as well as the overall capacity and loading. This technique is validated by application to the transport and retention of TiO2 nanoparticles in two vastly different porous filtration media—activated carbon and sand. TiO2 retained concentrations ranged from 0.24 to 0.37 mg g?1 for activated carbon and 0.01–0.014 mg g?1 for sand. The integrated method presented here is useful for both comparison of the filtration effectiveness of various porous materials as well as for process optimization and scale-up for industrial applications.  相似文献   

16.
堆肥过程中有机质和微生物群落的动态变化   总被引:3,自引:0,他引:3  
张园  耿春女  何承文  蔡超 《生态环境》2011,20(11):1745-1752
利用3个容积约为50 L的平行生物反应装置研究堆肥过程中温度、湿度(水分含量)、pH值和有机质的动态变化情况。按照Van Soest方法根据有机质不同的溶解特性将其分为:溶于沸水的有机质H2O、溶于中性试剂的有机质SOLU、半纤维素(HEMI)、纤维素(CELL)和木质素(LIGN)。结果表明:反应装置内环境湿度调控在60%左右时,堆肥系统内借助生化反应,温度最高可达到约50℃。堆肥材料在反应初期呈现偏酸性(pH=6.5),而随着反应的发生,pH逐渐变为中性或弱碱性(pH=7.4)。经过20 d的堆肥实验,有机质总量降解了约47%。在微生物作用下的各类有机质的降解率不同,按大小排序为H2O〉HEMI〉CELL〉SOLU〉LIGN,其降解率分别是85%、56%、36%、32%和27%。为了深入理解堆肥过程中有机质的降解机制,文章采用磷脂脂肪酸(PLFAs)技术对体系中的微生物群落变化进行了初步分析,发现微生物优势群落随反应温度的改变发生明显变化,在堆肥初期和堆肥中期,细菌占优势,而堆肥末期时真菌比例较高。在堆肥的过程中,革兰氏阴性菌的比例呈下降趋势,而革兰氏阳性菌的比例呈上升趋势。  相似文献   

17.
Plant uptake of inorganic and organic nitrogen: neighbor identity matters   总被引:5,自引:0,他引:5  
Miller AE  Bowman WD  Suding KN 《Ecology》2007,88(7):1832-1840
The importance of interspecific competition as a cause of resource partitioning among species has been widely assumed but rarely tested. Using neighbor removals in combination with 15N tracer additions in the field, we examined variation among three alpine species in the uptake of 15N-NH4+, 15N-NO3-, and 15N-13C-[2]-glycine in intact neighborhoods, when paired with a specific neighbor, and when all neighbors were removed. Species varied in the capacity to take up 15N-labeled NH4+, NO3-, and glycine in intact neighborhoods and in interspecific pairs. When interspecific neighbor pairs were compared with no neighbor controls, neighbors reduced 15N uptake in target species by as much as 50%, indicating competition for N. Furthermore, neighbor identity influenced the capacity of species to take up different forms of N. Thus, competition within interspecific neighbor pairs often caused reduced uptake of a particular form of N, as well as shifts to uptake of an alternative form of N. Such shifts in resource use as a result of competition are an implicit assumption in studies of resource partitioning but have rarely been documented. Our study suggests that plasticity in the uptake of different forms of N may be a mechanism by which cooccurring plants reduce competition for N.  相似文献   

18.
19.
垃圾填埋场渗滤液溶解性有机质特性及其去除技术综述   总被引:2,自引:0,他引:2  
垃圾填埋场渗滤液所含物质种类繁多,理化特性复杂,且随填埋时间等条件而变化.本文综合分析了垃圾渗滤液溶解性有机质的组成特征、结构特征及随年代变化特征.针对垃圾渗滤液难降解有机质的特性而研发的处理技术包括物化法、高级氧化法和微电解法等,并在实际工程中得到应用.随着越来越严格的渗滤液排放要求,溶解性有机质的去除应充分考虑投资的经济、运行的稳定性和可靠性.  相似文献   

20.
采用总有机碳分析仪、紫外-可见吸收光谱以及荧光激发-发射光谱(EEMs)对5种不同来源DOM与·OH的反应过程进行了表征,以考察DOM来源和类别对其与·OH反应的影响.结果表明,不同来源DOM与·OH的反应能力存在显著差异,陆源DOM比水源DOM表现出更强的反应能力.DOM与·OH的反应表现为准一级动力学,以DOC变化表征的反应速率常数kDOC与DOM的芳香碳/脂肪碳的比值(Caro/Cali)有较好的相关性,说明芳香性碳可能是·OH的优先反应位点.以光吸收参数Absave表征的衰减速率常数与kDOC也表现出良好的相关性.因来源与类别的差异,不同DOM不仅初始的EEMs存在差别,而且·OH氧化过程中EEMs的变化也表现出显著的不同.  相似文献   

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