Phytoremediation of landfill leachate using Pennisetum clandestinum

Landfills are still the most widely used solid waste disposal method used across the world. Leachate generated from landfill areas exerts environmental risks mostly on surface and groundwater, with its high pollutant content, most notably metals, which cause an unbearable lower water quality. During dumping or after the capacity of the landfill has been reached, a decontamination and remediation program should be taken for the area. This study was conducted to assess the capacity and efficiency of Pennisetum clandestinum, a prostrate perennial plant, to accumulate chromium (Cr), copper (Cu), iron (Fe), nickel (Ni), zinc (Zn) and lead (Pb). Leachate, taken from the Sofulu Landfill Site, was given to Pennisetum clandestinum for 180 days, in 3 dilution sets as 1/1, 1/2 and 1/4, in batch configuration. An additional control set was also installed for comparison. Results showed that, even though the metal content of soil had risen, plants accumulated 2 to 8.5 times higher concentrations than the control set. It is important to see, the plant showed almost no stress symptoms even if the set was fed by pure leachate. Pennisetum clandestinum was observed to accumulate metals mostly in the upper bodies, excluding Fe and Cu. 76% of accumulated Cr, 85% of Ni, 66% of Zn and 100% of Pb was observed to accumulate in above-ground parts, where only 20% of Cu and 4% of Fe was accumulated. Due to the high pollution tolerance of Pennisetum clandestinum, makes this plant suitable for decontamination and remediation of landfill sites.     

Anaerobic degradation kinetics of reactive dye with different carbon sources

This study aims to investigate the anaerobic degradation kinetics of reactive dye, C.I. Reactive Red 141 (Evercion Red H-E7B) by partially granulated anaerobic mixed culture using three carbon sources, namely modified starch (MS), polyvinyl alcohol (PVA) and acrylic size (AS) during batch incubation. There is a first-order kinetics reaction in the decolorization processes using MS and PVA as carbon sources, while a zero-order kinetics relationship describes the decolorization process for the AS carbon source. The k values and color removal rate of decolorization with MS carbon source was higher than those of PVA and AS carbon sources. This is because the MS carbon source was well degraded in comparison to AS and PVA, respectively This study also found dye reduction could be enhanced through the addition of MS as a carbon source. The decolorization rates increased with decrease in dye concentrations of RR 141. In contrast, the decolorization rates increased with increase in COD concentration.     

Anaerobic treatment of fresh leachate from a municipal solid waste incinerator by upflow blanket filter reactor

This paper describes the feasibility of fresh leachate treatment by an upflow blanket filter (UBF). Through dilution and partial effluent recycling, the organic loading rates increased from 0.51 to 14.56 kg COD/(m³·d), meanwhile the corresponding hydraulic retention time decreased from 9.0 to 3.6 d. The reactor was able to achieve steady-state within 80 d. Based on the distribution of COD fluxes in the process, it was concluded that anabolism was the main pathway of COD removal in the initial phase (1–33 d), accounting for 57%–85% of total COD removed. As the anaerobic consortium of bacteria reached steady-state (after 70–86 d), the majority of COD removed was transformed into methane, because the specific methane yield was close to the theoretical value (0.36 L CH₄/(g COD_deg)).     

Optimization of process parameters for mature landfill leachate pretreatment using MAP precipitation

Chemical precipitation is a useful technology as a pretreatment to treat mature landfill leachate with high concentrations of ammonium-nitrogen (NH4+-N) and refractory organic compounds. Orthogonal experiments and factorial experiments were carried out to determine the optimal conditions enhancing the magnesium ammonium phosphate (MAP) precipitation process, and the experimental results demonstrated that the removal rate of NH4+-N was more than 85% when MgO and NaH₂PO₄·2H₂O were applied as external sources of magnesium and phosphorous under the optimal conditions that molar ratio n(Mg)∶n(N)∶n(P) = 1.4∶1∶0.8, reaction time 60 min, original pH of leachate and settling time 30 min. In the precipitation process, pH could be maintained at the optimal range of 8–9.5 because MgO could release hydroxide ions to consume hydrogen ions. Calcium ions and carbonate ions existed in the leachate could affect the precipitation process, which resulted in the decrease of NH4+-N removal efficiency. The residues of MAP sediments decomposed by heating under alkaline conditions can be reused as the sources of phosphorous and magnesium for the removal of high concentrations of NH4+-N, and up to 90% of ammonium could be released under molar ratio of n[OH]∶n[MAP] = 2.5∶1, heating temperature 90°C and heating time 2h.     

Indicating landfill stabilization state by using leachate property from Laogang Refuse Landfill

Variation and evolution process of leachate can be applied as a reference for landfill stabilization phase. In this work, leachates with different ages were collected from Laogang Refuse Landfill, and characterized with 14 key parameters. Simultaneously, principal component analysis （PCA） was applied to develop a synthetic parameter-F based on these 14 parameters, and a logarithm equation was simulated for the landfill stabilization process finally. It was predicted that leachates would meet Class I and Class II in standard for pollution control on the landfill site of municipal solid waste （GB 16889-1997） after 32 years and 22 years disposal under the natural attenuation in the humid and warm southern areas of China, respectively. The predication of landfill state would be more accurate and useful according to the synthetic parameter F of leachate from a working landfill.     

Cr (VI) and Fe (III) removal using Cajanus cajan husk

Husk of tur dal (Cajanus cajan) was investigated as a new biosorbent for the removal of Fe (III) and Cr (VI) ions from aqueous solutions. Parameters like agitation time, adsorbent dosage and pH were studied at different initial Fe (III) and Cr (VI) concentrations. The biosorptive capacity of the Tur dal husk was dependent on the pH of the chromium and iron solution, with pH 2 and 2.5 respectively being optimal. The adsorption data fit well with Langmuir and Freundlich isotherm models. The practical limiting adsorption capacity (qmax) calculated from the Langmuir isotherm was 96.05 mg of Cr(VI)/ g of the biosorbent at an initial pH of 2.0 and 66.65 mg/g at pH 2.5. The infrared spectra of the biomass revealed that hydroxyl, carboxyl and amide bonds are involved in the uptake of Cr (VI) and Fe (III) ions. Characterisation of tur dal husk has revealed that it is an excellent material for treating wastewaters containing low concentration of metal ions.     

Photocatalytic degradation of phosphamidon using Ag-doped ZnO nanorods

The photocatalytic degradation of the organo-phosphorous pesticide phosphamidon at low concentration in aqueous solution on Ag-doped ZnO nanorods was investigated. Nanosized Ag-doped ZnO rods were synthesized by using a microwave assisted aqueous method. High molecular weight polyvinyl alcohol was used as a stabilizing agent. Composition and structure were investigated using energy-dispersive X-ray spectroscopy (EDAX) and X-ray diffraction (XRD). The XRD pattern reveals that ZnO nanorods are of hexagonal wurtzite structure. The average crystallite size calculated from Scherrer's relation was found to be 30?nm. The effects of catalyst loading, pH value, and initial concentration of phosphamidon on the photocatalytic degradation efficiency using Ag-doped ZnO nanorods as a photocatalyst have been discussed. The results revealed that Ag-doped ZnO nanorods with a diameter of 30?nm showed highest photocatalytic activity at a surface density of 1?g?dm^?3. The catalyst doped with 0.2?mol% Ag is effective for the degradation of phosphamidon with visible light. This opens a new possibility to decompose pesticides that are present in wastewater.     

Photocatalytic degradation of methyl orange using ZnO nanorods

Nanosized ZnO rods were synthesized using a microwave-assisted aqueous method. High molecular weight polyvinyl alcohol was used as a stabilizing agent. Size, surface morphology, and structure were investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). SEM and TEM images show that ZnO nanorods have diameters of about 50?nm and lengths of a few micrometers. The XRD pattern reveals that ZnO nanorods are of hexagonal wurtzite structure. The average crystallite size calculated from Scherrer's relation was found to be 40?nm. The effects of catalyst loading, pH value, and initial concentration of methyl orange on the photocatalytic degradation efficiency using ZnO nanorods as photocatalyst were discussed. The results revealed that ZnO nanorods with a diameter of 50?nm showed the highest photocatalytic activity at a surface density of 0.2?g?dm^?3.     

利用矿化垃圾层预防和控制渗滤液导排系统堵塞

在卫生填埋场中,垃圾渗滤液导排系统堵塞普遍存在,悬浮固体形成的物理堵塞、有机物降解和金属离子沉淀导致的生物.化学堵塞是引起导排系统堵塞的关键因素.本文构建了"矿化垃圾+砾石层导排"的渗滤液下渗装置,通过矿化垃圾预处理渗滤液中悬浮固体和有机物以控制导排系统发生的物理和生物-化学堵塞.结果表明,在矿化垃圾层,渗滤液中化学需...     

与环境污染物转化相关的细菌厌氧呼吸研究动态

基于细菌呼吸理论为基础的环境有毒物质降解为环境污染治理提供了新的策略和方法,是近年来研究的热点问题.细菌呼吸是自然界中一个最基本、最重要的生物代谢过程,具有很大的灵活性和多样性,且与生态环境密切相关.在厌氧条件下,细菌利用环境中多种有毒物质作为呼吸链末端电子受体进行厌氧呼吸,在有毒物质被还原甚至降解的同时实现电子在呼吸链上的传递,形成跨膜的质子浓度电势梯度,进而转化为其生长代谢所需的能量.细菌以环境有毒物质为电子受体的厌氧呼吸不断被发现,这对于深入理解细菌呼吸的本质具有重要的理论意义,同时对于有毒物质的降解及元素的生物地球化学循环具重要的环境学意义,对于提高对地球表面有毒物质污染生物修复策略的认识具有重要的现实意义.图1表1参45     

Potential of rice husk ash in atrazine removal

An experimental study was carried out to explore the possibility of using a prepared microporous material, Rice Husk Ash (RHA) as an alternative to the commercial Powdered Activated Carbon (PAC), to remove atrazine (ATZ) pesticide from aqueous solution. The effects of contact time and pH on the adsorption were studied using the batch technique. Based on Hückel model calculations, the zwitterion behaviour of atrazine molecule was proved to be related to the pH of zero charge point of adsorbents (6.8 for RHA and 8.2 for PAC). The results showed that the Pseudo Second Order model is applicable to both adsorbents, suggesting that chemisorption is the rate-limiting step. The equilibrium data fitted well with the Langmuir model in the case of RHA, whereas the Freundlich model better fitted the equilibrium data in the PAC case, suggesting the existence of multi-layer adsorption of atrazine. The adsorption for RHA was found to be feasible and spontaneous, with a removal capacity of atrazine of more than 7?mg?g^?1. With regard to the BET surface, this removal capacity (50.5?µg_ATZ / m²_RHA) was 25% better than that PAC (37.75µg_ATZ / m²_PAC).     

垃圾渗滤液的Fenton氧化预处理研究

采用Fenton氧化法对垃圾渗滤液进行预处理,考察了渗滤液初始pH值、H2O2和FeSO4.7H2O投加量、H2O2/Fe2＋投加的物质的量比及氧化反应时间等对Fenton氧化处理效果的影响,获得Fenton氧化处理垃圾渗滤液的最佳工艺条件：初始pH=3.0,H2O2投加量为5.0 mL.L-1,FeSO4.7H2O投加量为3.48 g.L-1,H2O2/Fe2＋物质的量比为4-1,反应时间为1.5 h。最佳条件下处理后垃圾渗滤液COD为5 220 mg.L-1,COD去除率达57.8%。凝胶渗透色谱和三维荧光光谱分析结果表明,垃圾渗滤液中主要含有腐殖酸类大分子物质,经Fenton氧化后降解变成小分子化合物。     

三维电极体系中苯酚降解效率的影响因素研究

三维电极法用于处理含酚废水的影响因素研究报道较多,但并未充分在理论上阐述其影响方式及机理。采用自制的实验室小试电化学反应器对含酚自配废水进行了处理。试验结果表明:体系中苯酚降解遵循一级反应模式;通过电流效率的核算确定60min作为最佳反应时间,得到的苯酚去除率为64.3%,吨水处理能耗为14.29kW·h·t-1,实际电流效率与理论电流效率相等为0.68。对体系进水控制不同的苯酚起始质量浓度,当反应时间不变时,实际试验结果与法拉第定律一致,即电流密度与去除的污染物的量以及COD去除率与电量和进水质量浓度的比值均呈线性关系;体系中羟基自由基的产生量能够采用式[?OH]=0.1218×EC0进行计算。采用最佳反应时间t=60min、电流密度I=20A,在苯酚质量浓度为500mg·L-1时改变极板间距进行的试验结果表明电压随极板间距的增大而降低,最佳极板间距为0.21m时可获得最大去除率为78.5%,体系的启动电压为0.25V。     

Photocatalytic degradation of methyl orange using ZnO/TiO composites

ZnO/TiO₂ composites were synthesized by using the solvothermal method and ultrasonic precipitation followed by heat treatment in order to investigate their photocatalytic degradation of methyl orange (MO) in aqueous suspension under UV irradiation. The composition and surface structure of the catalyst were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission electron microscopy (TEM). The degradation efficiencies of MO at various pH values were obtained. The highest degradation efficiencies were obtained before 30min and after 60min at pH 11.0 and pH 2.0, respectively. A sample analysis was conducted using liquid chromatography coupled with electrospray ionization ion-trap mass spectrometry. Six intermediates were found during the photocatalytic degradation process of quinonoid MO. The degradation pathway of quinonoid MO was also proposed.     

温度对填埋垃圾渗滤液特征的影响

温度对填埋场有机垃圾的厌氧降解具有十分重要的影响,因而对填埋场渗滤液特征也产生重要的影响。文章通过在常温及29~45℃范围内设置的6个不同温度下的模拟垃圾柱降解对照试验,分析研究了温度对填埋有机垃圾渗滤液特征的影响。结果表明,在垃圾降解适宜的温度范围(29~45℃)内,较高的温度对渗滤液COD衰减具有较大的促进作用,而保持恒定的温度比升高温度对渗滤液COD衰减的影响更加显著,但温度对垃圾降解渗滤液中氨氮影响并不明显。     

应用HYDRUS-1D模型模拟农田土壤水渗漏及硝态氮淋失特征

在定位试验基础上,应用HYDRUS-1D模型对黄淮海平原典型土壤(黄潮土)中土壤水渗漏及硝态氮淋失动态进行了模拟分析。结果表明:在传统水氮管理模式下,黄潮土2m土体深处的土壤水渗漏和硝态氮淋失非常严重,2个轮作期内,土壤水渗漏总量占地表总入水量的23.7%,硝态氮淋失总量占总输入N量的15.9%,冬小麦生长季的硝态氮淋失量大于夏玉米生长季;改良灌溉和改良施肥模式下产生的硝态氮淋失量比传统灌溉和传统施肥模式减少74.7%,节约灌溉水211.5mm、节省施N423.5kg·hm-2。     

Photocatalytic degradation of phenol in water using TiO2 and ZnO

Photocatalytic degradation of chemical pollutants in water was investigated using semiconductor oxide catalysts, zinc oxide (ZnO) and titanium dioxide (TiO2) and phenol as the substrate. Influence of various parameters such as characteristics of the catalyst, irradiation time, substrate and catalyst concentrations, pH etc. has been studied and optimum conditions for the complete degradation of phenol in water have been identified. In terms of activity and durability TiO2 is far superior to ZnO. Mixing ZnO with TiO2 does not affect its activity significantly. The process is especially relevant in view of its potential for the treatment of wastewater containing pollutants, using solar radiation as the energy source.     

Photocatalytic degradation of methyl orange using ZnO/TiO2 composites

ZnO/TiO₂ composites were synthesized by using the solvothermal method and ultrasonic precipitation followed by heat treatment in order to investigate their photocatalytic degradation of methyl orange (MO) in aqueous suspension under UV irradiation. The composition and surface structure of the catalyst were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission electron microscopy (TEM). The degradation efficiencies of MO at various pH values were obtained. The highest degradation efficiencies were obtained before 30 min and after 60 min at pH 11.0 and pH 2.0, respectively. A sample analysis was conducted using liquid chromatography coupled with electrospray ionization ion-trap mass spectrometry. Six intermediates were found during the photocatalytic degradation process of quinonoid MO. The degradation pathway of quinonoid MO was also proposed.     

垃圾填埋场渗滤液地下原位脱氮技术综述

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。