微波诱导AC/Cu、AC/Fe催化非均相Fenton 反应催化降解垃圾渗滤液

采用活性炭载体负载Cu、Fe为催化剂,在微波诱导作用下,对垃圾渗滤液污染物进行降解。实验结果表明,活性炭负载金属前经适当浓度硝酸浸泡处理后,催化剂对COD去除率提高可超过15%,过高硝酸盐浓度对COD去除有不利影响;催化剂对COD去除率随Cu、Fe金属负载量增加呈先增加后降低的趋势,催化剂对Cu、Fe的最佳负载量分别为质量百分比2.11%和1.12%。对于AC-Cu体系,在初始pH=3,H2O2投加量为4.98×103mg/L,催化剂用量为5.0×103mg/L,420 W功率下微波辐射10 min时,垃圾渗滤液COD去除率可达到84.13%;对于AC-Fe体系,当H2O2投加量为0.33×103mg/L,催化剂AC-Fe用量为2.0×104mg/L,420 W功率下微波作用10 min时,垃圾渗滤液COD去除率为60.16%。分析2种催化剂对COD去除差异的原因,可能是催化剂AC-Cu表面单分子分布的阈值比AC-Fe高。降解液的pH值对AC-Cu体系、AC-Fe体系COD去除影响存在拐点,最高COD去除率点对应的降解液pH值为3。微波辐射功率较低时,体系COD去除率随辐射功率增加而增加;辐射功率较高时,高温下垃圾渗滤液中有机硫化物分解成小分子硫化物,对催化剂活性存在一定抑制作用。     

Organic-coated nanoparticulate zero valent iron for remediation of chemical oxygen demand (COD) and dissolved metals from tropical landfill leachate

The use of nanoparticulate zero valent iron (NZVI) in the treatment of inorganic contaminants in landfill leachate and polluted plumes has been the subject of many studies, especially in temperate, developed countries. However, NZVI’s potential for reduction of chemical oxygen demand (COD) and treatment of metal ion mixtures has not been explored in detail. We investigated the efficiency of NZVI synthesized in the presence of starch, mercaptoacetic, mercaptosuccinic, or mercaptopropenoic acid for the reduction of COD, nutrients, and metal ions from landfill leachate in tropical Sri Lanka. Synthesized NZVI were characterized with X-ray diffraction (XRD), transmission electron microscopy, X-ray photoelectron spectroscopy, scanning electron microscopy (SEM), thermal gravimetric analysis, Fourier transform infrared spectroscopy (FTIR) and Brunauer–Emmett–Teller. Of the samples tested, Starch-NZVI (S-NZVI) and mercaptoacetic-NZVI (MA-NZVI) performed well for treatment both COD and metal mixture. The removal percentages for COD, nitrate-nitrogen, and phosphate from S-NZVI were 50, 88, and 99 %, respectively. Heavy metal removal was higher in S-NZVI (>95 %) than others. MA-NZVI, its oxidation products, and functional groups of its coating showed the maximum removal amounts for both Cu (56.27 mg g^?1) and Zn (28.38 mg g^?1). All mercapto-NZVI showed well-stabilized nature under FTIR and XRD investigations. Therefore, we suggest mercapto acids as better agents to enhance the air stability for NZVI since chemically bonded thiol and carbonyl groups actively participation for stabilization process.     

垃圾填埋场渗滤液物化深度处理研究

通过Fenton法和结合聚合硫酸铁的混凝作用，实现垃圾渗滤液氧化塘出水COD的深度处理；并利用水泥水化产物的凝胶物质，强化COD去除率。30％H2O2投加量为0．75mL／L、七水硫酸亚铁投加量为1．5g／L、n（H2O2）：n（Fe^2＋）=1．2：1（摩尔比）时，Fenton法对渗滤液COD的去除率可达52％；水灰比为2：1、搅拌24h的水泥水化物将Fenton法的出水pH值从4调至10，该工艺流程总的COD去除率为73．6％，较普通的Ca（OH）2调节法提高9．3％，出水COD可以从进水的1200mg／L降至315mg／L。     

准好氧矿化垃圾反应床＋超声／芬顿联用技术处理垃圾渗滤液

针对垃圾渗滤液污染物浓度高、可生化性差等特点，采用准好氧矿化垃圾反应床＋超声／芬顿联用技术对垃圾渗滤液进行预处理。准好氧矿化垃圾床处理后渗滤液中COD、氨氮、总磷、色度的去除率分别为80％、85％、92％和85％。通过单因素实验和正交实验，确定了超声／Fenton法最佳工艺条件。经该组合工艺后，渗滤液中COD、氨氮、总磷和色度的最高去除率分别可达96％、86％、94％和95％，且出水无臭，颜色为淡黄色，BOD5／COD从0．16增至0．35左右，可生化性基本满足后续生物处理需要，且COD、总磷这2个指标达到《生活垃圾填埋场污染控制标准》（GB16889—2008）规定的排放标准。     

垃圾渗滤液生化出水的脱色研究

分别采用脉冲电解法、混凝沉淀法、芬顿氧化法、高铁酸钾氧化法对垃圾渗滤液生化出水进行处理，考察了处理效果。结果表明：铁电极电解法和芬顿试剂氧化法均能脱除垃圾渗滤液的色度，去除有机物质。铁电极电解对色度的去除率可达98．4％，COD去除率可达84．4％；芬顿试剂氧化对色度的去除率可达99％，COD去除率可达85．8％。两种方法均能使出水达到排放标准。同时比较了各种处理方法的运行成本，在达到同样出水标准的前提下，铁电极电解运行成本远低于芬顿试剂氧化，为3．67元／t水，而芬顿试剂药剂成本为8．67元／t水。     

Fenton氧化降解垃圾渗滤液中COD的动力学研究

对絮凝预处理后的垃圾渗滤液进行Fenton氧化处理。通过微分法对Fenton氧化的反应级数进行求解,确定其反应级数为2,并初步建立了Fenton氧化的动力学模型,即1/c=1/c0+kt,由此建立起来的降解的动力学模型与实验数据相吻合;在4个实验基准条件下———初始COD浓度为960 mg/L、pH值4、H2O2投加量0.4 mol/L、nH2O2/nFe2+3∶1,探讨了其中某一变量对反应速率的影响。实验水样为絮凝反应出水,进水COD浓度为912～960 mg/L,出水COD浓度为80～112 mg/L,COD去除率在87%～92%之间,表明Fenton试剂能够有效地处理垃圾渗滤液。     

Elimination of radiocontrast agent diatrizoic acid by photo-Fenton process and enhanced treatment by coupling with electro-Fenton process

The removal of radiocontrast agent diatrizoic acid (DIA) from water was performed using photo-Fenton (PF) process. First, the effect of H₂O₂ dosage on mineralization efficiency was determined using ultraviolet (UV) irradiation. The system reached a maximum mineralization degree of 60 % total organic carbon (TOC) removal at 4 h with 20 mM initial H₂O₂ concentration while further concentration values led to a decrease in TOC abatement efficiency. Then, the effect of different concentrations of Fenton’s reagents was studied for homogeneous Fenton process. Obtained results revealed that 0.25 mM Fe³⁺ and 20 mM H₂O₂ were the best conditions, achieving 80 % TOC removal efficiency at 4 h treatment. Furthermore, heterogeneous PF treatment was developed using iron-activated carbon as catalyst. It was demonstrated that this catalyst is a promising option, reaching 67 % of TOC removal within 4 h treatment without formation of iron leachate in the medium. In addition, two strategies of enhancement for process efficiency are proposed: coupling of PF with electro-Fenton (EF) process in two ways: photoelectro-Fenton (PEF) or PF followed by EF (PF-EF) treatments, achieving in both cases the complete mineralization of DIA solution within only 2 h. Finally, the Microtox tests revealed the formation of more toxic compounds than the initial DIA during PF process, while, it was possible to reach total mineralization by both proposed alternatives (PEF or PF-EF) and thus to remove the toxicity of DIA solution.     

城市生活垃圾填埋场渗滤液生化处理过程中重金属离子问题

我国对城市生活填埋场渗滤液处理技术的研究主要集中在COD与NH4 -N的去除上,对渗滤液中重金属离子的专项研究几乎未见报道.本文首先总结了国内外城市生活垃圾渗滤液中重金属的种类及浓度,在渗滤液中的存在状态,渗滤液中重金属与其他成分(有机物、氨氮)的相互作用关系,辨证分析了重金属在渗滤液生化处理过程中的有益作用和毒性,归纳了重金属在渗滤液生化处理过程中的变化规律,同时总结分析了重金属的去除技术.     

混凝与Fenton联用处理垃圾渗滤液的效能及成本

为对混凝/Fenton工艺与Fenton/混凝工艺处理垃圾渗滤液的效果和成本进行比较,分别对年轻渗滤液和老龄渗滤液原液按照混凝/Fenton工艺与Fenton/混凝工艺2种技术路线进行处理。实验结果表明,Fenton试剂对年轻垃圾渗滤液和老龄垃圾渗滤液COD去除率最高的反应条件为pH=3.5、H2O2和Fe2+的摩尔比为6、H2O2和渗滤液原液的COD质量比为3、反应时间4 h;在PAC与渗滤液原液的COD质量比为0.6时,PAC混凝对渗滤液原液的COD去除率最高。在对渗滤液COD去除率最高的Fenton反应和PAC混凝反应条件下,混凝/Fenton工艺对年轻渗滤液和老龄渗滤液的COD去除率分别为90.56%和86.56%;Fenton/混凝工艺对年轻渗滤液和老龄渗滤液的COD去除率分别为89.99%和85.99%,2种技术路线对渗滤液COD的去除率相差不大,但先PAC混凝后Fenton氧化工艺比先Fenton后混凝工艺每t节省62.6元,是更优化的渗滤液处理工艺。     

回灌型准好氧填埋场脱氮特性及加速稳定化研究

采用2个模拟填埋生物反应器,1号柱渗滤液简单回灌,2号柱为渗滤液回灌准好氧联合运行方式,研究了渗滤液回灌准好氧生物反应器填埋场的脱氮特性及加速垃圾稳定化特性.研究结果表明:渗滤液回灌准好氧填埋场具有很强的脱氮能力,2号柱由厌氧运行方式改为准好氧条件下,渗滤液中的氨氮和凯式氮浓度分别由最大值的3 198 mg/L和3 345 mg/L降低到第160 d的73 mg/L和81 mg/L,去除率分别为97.7%和97.6%,pH快速升高到8.0左右,COD浓度快速降低.渗滤液中溶解性有机物(DOM)分级结果表明,2号柱HA和FA含量的增加明显快于1号柱.2号柱DOM的三维荧光光谱特性发生了较大变化,荧光基团从60 d结构简单的类蛋白物质转变为95 d结构复杂的类胡敏酸和富里酸物质,而l号柱渗滤液DOM荧光基团一直是结构简单的类蛋白物质.结果表明回灌准好氧生物反应器填埋场的稳定化速度远快于简单回灌的生物反应器填埋场.     

Treatment of landfill leachate by electrochemical oxidation and anaerobic process.

The removal performance of typical refractory organic compounds in landfill leachate was investigated during the electrochemical (EC) oxidation and anaerobic process combined treatment system in this paper. The results indicated that the treatment of landfill leachate by the combined system was highly effective. The toxicity of leachate was notably decreased after the electrochemical oxidation process and the biodegradability was improved. The concentration of the organic acid with low molecular weight in the leachate increased from 28% to 90% based on the biodegradability assays after the EC oxidation process. The anaerobic digestion could further remove the residual organic compounds. At a hydraulic retention time (HRT) of 16 hours and an organic loading rate (OLR) of 8 kg COD/m3 d, the concentration of COD, SS, ALK, VA, N-TKN, N-NH4+ and P-PO4(3)- [corrected] in UASB effluent were 532, 12, 6744, 400, 540, 455 and 11.6 mg/L, respectively, with approximately 90% removal efficiency of COD. The organic compounds in the landfill leachate revealed different degradation characteristics in the combined system. p-chloroaniline, bisphenol A, 6-methyl-2-phenyl-quinoline, dimethylnaphthaline and N'-(2-methyl-4-chlorophenyl)-N-cyclohexyformamidine, classified into the first group in this paper, were completely removed by the EC oxidation and did not reappear in the effluent of the UASB reactor. Phenylacetic acid, 3-methyl-indole and N-cyclohexyl-acetamide, called the second group, were completely removed, but reappeared in the UASB reactor. 4-methyl-phenol, 3,4-dihydroisoquinoline, 2(3H)-benzothiazolone, exo-2-hydroxycineole and benzothiazole, the third group, were degraded little in the EC oxidation process, but extensively removed by the anaerobic process. Benzoic acid, benzenepropanoic acid and 2-cyano-3,5-dimethyl-1-hydroxypyrrole, the fourth group, concentration obviously increased in the EC process, but was completely removed in the UASB reactor. The content of volatile fatty acids (VFAs) markedly increased from 0.68% in the leachate to 16.18% in the effluent from the electrochemical oxidation process (EC(effl)). In addition, the degradation rate of organic compounds from the landfill leachate was different in the EC oxidation and anaerobic process.     

“老龄期”填埋场渗滤液COD蒸发规律研究

“老龄期”填埋场渗滤液由于可生化性差而难于处理。采用常规蒸发、减压蒸发和载气蒸发处理不同pH值的“老龄期”渗滤液。实验结果表明，3种蒸发方式下，冷凝液CODF降过程中均存在明显的浓度转折点，转折点之后COD维持较低水平，为“老龄期”渗滤液的“三分处理法”提供理论依据。与常规蒸发相比，减压蒸发和载气蒸发的前期冷凝液COD较高，且浓度转折点偏后。     

"老龄期"填埋场渗滤液COD蒸发规律研究

"老龄期"填埋场渗滤液由于可生化性差而难于处理.采用常规蒸发、减压蒸发和载气蒸发处理不同pH值的"老龄期"渗滤液.实验结果表明,3种蒸发方式下,冷凝液COD下降过程中均存在明显的浓度转折点,转折点之后COD维持较低水平,为"老龄期"渗滤液的"三分处理法"提供理论依据.与常规蒸发相比,减压蒸发和载气蒸发的前期冷凝液COD较高,且浓度转折点偏后.     

渗滤液回灌频率对生物反应器填埋场的影响研究

通过模拟实验研究了渗滤液回灌周期为1、2、3和5 d的4个模拟垃圾柱的产甲烷过程和渗滤液水质的变化情况.在用NaOH调节回灌渗滤液pH值的前提下,回灌频率越高,模拟厌氧型生物反应器填埋垃圾柱先开始产甲烷,但当回灌周期低于3 d时,开始产甲烷的时间相差不多.从渗滤液水质看,回灌周期为3 d的垃圾柱渗滤液COD、VFA等有机污染物浓度下降最快.综合考虑启动时间、运行费用和填埋场的稳定进程,在厌氧型生物反应器填埋场中,实施3 d/次的渗滤液回灌频率最为合适.     

厌氧陈腐垃圾模拟柱对渗滤液COD和NH_3-N的处理特性

通过实地钻取阿苏卫填埋场陈腐垃圾,真实模拟填埋场压实工艺,制作2种不同压实密度的陈腐垃圾模拟柱,对比研究其对渗滤液COD、NH3-N处理效果。结果表明,当模拟柱压实密度为1.09 t/m3时,渗滤液垂直运动明显;回灌此模拟柱水力负荷分别为18.6、28、37.2和46.5 L/t时,COD去除效果稳定,平均去除率达82.4%,最高去除率可达90.1%;出水NH3-N浓度均值为549.3 mg/L,且介于415～700 mg/L间变化。自循环回灌COD去除率最高仅为11.5%,NH3-N去除率最高仅为11.8%,两者去除效果不明显。因此,北方平原型填埋场进一步完善填埋工艺,使填埋场垂直方向渗透系数分布均匀,充分利用陈腐垃圾堆体的自降解能力,才是处理渗滤液污染的关键。     

二氧化氯深度处理垃圾渗滤液研究

利用二氧化氯对生物处理后的垃圾渗滤液进行深度处理，根据废水中有效氯浓度、COD、氨氮及细菌数等参数的分析，初步探讨了不同浓度的二氧化氯在不同处理时间内对垃圾渗滤液的处理效果。结果表明，对于COD初始浓度为450 mg/L左右的水样，二氧化氯的投加浓度达100 mg/L（有效氯），反应时间在50 min时，处理水样可达到同类废水的国家二级排放标准；对于同样条件下的水样，当加入约25 mg/L的二氧化氯时可以杀灭水样中的大肠杆菌，加入浓度达到90 mg/L的二氧化氯时，可以杀灭水样中几乎所有的细菌。     

生化-调碱后垃圾渗滤液的Fenton深度处理效果

针对上海老港垃圾填埋场经过厌氧-曝气塘处理后的渗滤液难进一步处理的问题,对其采用厌氧滤池-好氧接触法、氧化钙2种方式预处理,在此预处理基础上,考察了Fenton法深度处理的效果,探讨了H2O2/Fe2+投加比、初始pH、H2O2投加量、反应时间和Fenton试剂投加方式对渗滤液COD去除效果的影响。研究发现:经过生物预处理后,渗滤液的COD和TP分别降低了24%和25%;氧化钙调碱可以进一步使COD和TP去除率分别达到42%和96%;后续Fenton深度氧化的最佳条件为:初始pH为2,H2O2投加量为2.4 g/L,H2O2/Fe2+摩尔比为5∶1,Fenton试剂一次投加,反应时间为2 h。在此条件下,渗滤液的COD从1 340 mg/L降到198 mg/L,总COD去除率达到85%。     

太阳光Fenton法处理垃圾渗滤液中有机污染物

研究利用太阳光Fenton法处理垃圾渗滤液。根据太阳光辐射强度随时间的变化规律，选择重庆7、8月份的晴天，在中午12：00到下午14：00时进行试验，研究太阳光辐射时间、pH值、Fenton试剂用量对垃圾渗滤液COD去除率的影响。研究结果表明：太阳光Fenton法对垃圾渗滤液的COD有较好的去除效果，COD去除率达86.2%。太阳光Fenton法处理垃圾渗滤液的优化条件是：日光辐射时间为120 min，pH值为2.5，Fe²⁺浓度为5 mmol/L，H₂O₂浓度为570 mmol/L。同时，论文还对太阳光Fenton法处理垃圾渗滤液的动力学进行分析。研究结果显示：太阳光Fenton法处理垃圾渗滤液，其表观动力学方程为-dC/dt=2.6×10^-8×P^1.92×F^1.79×E^1.67。     

两级UASB与好氧组合工艺处理城市生活垃圾渗滤液的启动研究

采用两级UASB与好氧组合工艺处理早期城市生活垃圾渗滤液.系统出水按不同比例回流到一级UASB中进行反硝化,同时进行产甲烷反应,有机物在二级UASB中被进一步降解,好氧池完成剩余有机物的去除和氨氮的硝化.启动阶段通过对原渗滤液不同比例的稀释,分5次逐步提高进水浓度,启动结束时完成了对原渗滤液的高效处理.在进水COD浓度从3000 mg/L提高到15000 mg/L,氨氮浓度从250 mg/L提高到1400 mg/L时,最终COD去除率稳定在92%左右,氨氮去除率可达99%以上,一级UASB中反硝化率接近100%,回流比为300%时系统总氮去除率为70%～80%.     

Decomposition of non-ionic surfactant Tergitol TMN-10 by the Fenton process in the presence of iron oxide nanoparticles

The aim of our studies was to determine the efficiency of decomposition of non-ionic surfactant by the Fenton method in the presence of iron nanocompounds and to compare it with the classical Fenton method. The subject of studies was water solutions of non-ionic detergent Tergitol TMN-10 used in textile industry. Water solutions of the surfactant were subjected to treatment by the classical Fenton method and to treatment in the presence of iron nanocompounds. In the samples of liquid solutions containing the surfactant, chemical oxygen demand (COD) and total organic carbon (TOC) were determined. The Fenton process was optimized based on studies of the effect of compounds used in the treatment, doses of iron and nanoiron, hydrogen peroxide and pH of the solution on surfactant decomposition. Iron oxide nanopowder catalyzed the process of detergent decomposition, increasing its efficiency and the degree of mineralization. It was found that the efficiency of the surfactant decomposition in the process with the use of iron nanocompounds was by 10 to 30 % higher than that in the classical method. The amounts of formed deposits were also several times smaller.