北方城市垃圾渗滤液水量水质变化特征

研究了垃圾卫生填埋场渗滤液的年产量、夏季产量及其与填埋场规模、运行年限之间的关系。分析了填埋场夏季渗滤液的COD、BOD5、氨氮、p H值和BOD5/COD规律。研究结果表明,渗滤液年产量与填埋场规模、运行年限有关。渗滤液夏季产量变化规律与其相应的年产量并不一致。规模M≤100 t/d、100M≤200 t/d、200M≤500 t/d和M500 t/d的填埋场夏季渗滤液产量呈现出不同的变化特征。各填埋场的夏季渗滤液水质差别较大,COD值总体偏小,处于35.5~3 029.8 mg/L之间;BOD5值处于6.5~1 120.7 mg/L之间;64.2%的填埋场夏季渗滤液的BOD5/COD值≥0.30,可生化性较好;氨氮为21~1 273 mg/L。研究结果可为国内城市垃圾卫生填埋场渗滤液处理工作提供参考。     

电化学氧化法处理垃圾渗滤液纳滤浓缩液

实验利用电化学氧化法处理垃圾渗滤液纳滤浓缩液,以提高废水的可生化性。研究考察了水力停留时间、进水流量、循环流量、电流强度和原水氯离子浓度对有机物去除的影响。研究结果表明,电化学氧化法的最佳运行条件如下:水力停留时间为3 h,进水流量为1 m3/h,循环流量为15 m3/h,电流强度为420 A。在上述条件下,原水COD浓度从3 100mg/L降到1 311.3 mg/L,去除率达到57.7%,BOD/COD值由0.03提升至0.31。氯离子对电解有促进作用,但原水氯离子浓度超过5 000 mg/L,不需要外加工业盐。     

强化混凝-光电氧化组合工艺深度处理垃圾渗滤液膜滤浓缩液

采用强化混凝-光电氧化组合工艺对北京某垃圾填埋场垃圾渗滤液膜滤浓缩液进行处理。探讨了不同混凝剂投加量、电流密度和反应时间对COD去除率的影响,并考察了溶解性有机物的分子量和结构在本工艺中的变化。结果表明:同时投加Ca(OH)2、Fe2(SO4)3和PAM混凝后,COD去除率为28.00%,含量由4 700 mg/L降低到3 384 mg/L;同时投加KMnO4、Fe2(SO4)3和PAM进行二次混凝,COD去除率为60.20%,含量为1 870 mg/L;混凝后水样在电流密度为400A/m2,经3 h光电氧化后,COD去除率为86.20%,含量为650 mg/L。本工艺将垃圾渗滤液膜滤浓缩液中部分大分子量有机物降解为小分子量有机物;光电氧化后,有机物结构被迅速破坏。     

臭氧预氧化-BAF工艺深度处理垃圾渗滤液

以广东省江门市垃圾填埋场垃圾渗滤液为研究对象，对经SBR生化处理和聚合硫酸铁混凝后的垃圾渗滤液，采用臭氧-BAF(曝气生物滤池)工艺进行深度处理。该工艺优点在于：臭氧高级氧化技术使大分子有机污染物降解成二氧化碳和水，或者小分子有机污染物，有利于后继BAF的生化处理，且臭氧处理过后废水的色度明显降低，是废水处理的有效方法之一。而后采用曝气生物滤池对垃圾渗滤液进行进一步处理，对COD进一步去除。结果表明，当臭氧的加入量为150 mg/L，BAF停留时间＞4 h，出水COD低于85 mg/L，稳定达到国家GB 16889-1997《生活垃圾填埋污染控制标准》一级排放标准，臭氧氧化法处理每吨垃圾渗滤液的费用为4.8元。     

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.     

光电芬顿氧化法深度处理垃圾渗滤液研究

采用光电芬顿氧化法对北京市某垃圾填埋场已经生化处理后的垃圾渗滤液进行深度处理，分别考察了电流强度和铁的不同价态等因素对渗滤液总有机碳（TOC）、化学需氧量（COD）以及色度去除效果的影响，并对阳极氧化、电芬顿和光电芬顿不同反应过程进行了对比。通过分析渗滤液UV-Vis光谱(200～500 nm)变化和渗滤液中有机污染物的分子量变化，发现光电芬顿反应可以明显改善渗滤液生化性。深入研究了反应过程中铁价态的变化规律。试验结果发现，以高比表面积的活性炭纤维(ACF)为阴极的光电芬顿反应可以有效降解垃圾渗滤液，在pH为3，Fe²⁺ 浓度为1 mmol/L，电流为0.5 A，O₂通入量为250 mL/min条件下降解360 min，垃圾渗滤液TOC和COD去除率分别达到78.9%和62.8%，色度完全去除。     

回灌对垃圾填埋初期渗滤液化学需氧量的影响

通过模拟柱实验 ,研究了回灌对垃圾填埋场初期渗滤液 CODCr的影响。研究结果表明 ,模拟降雨雨水的渗入且无渗滤液回灌的参照柱 ,其渗滤液出水 CODCr最高 ,一般在 70 0 0 0 mg/L 左右 ;模拟渗滤液原液回灌 ,从第 4周起因脂肪酸的积累导致渗滤液的 p H低于 6,从而抑制了微生物的生化反应 ;模拟好氧生物处理后渗滤液的回灌 ,能加速垃圾层 CODCr的溶出和甲烷化阶段的建立 ,且此时渗滤液的 CODCr变化规律符合指数方程 ;当垃圾层建立甲烷化阶段后 ,回灌 CODCr在 2 0 0 0 0 m g/L 左右的渗滤液 ,仍可促使垃圾中有机物迅速转化为气态物     

氧分压对催化湿法氧化法去除垃圾渗滤液TOC的影响

采用催化湿法氧化法 ( CWAO)降解垃圾填埋场渗滤液 ,研究了不同温度下氧分压对去除渗滤液中总有机碳 ( TOC)的影响。结果表明 ,2 4 0℃以下 ,氧分压升高 ,TOC去除率缓慢上升 ,2 6 0℃以上时 ,大于 1.5 MPa的氧分压对去除 TOC效率的影响较小 ,即进一步实验所需最佳氧分压为 1.5MPa。此外 ,不同氧分压下 CWAO降解垃圾渗滤液的动力学符合 Elovich方程     

SBR法处理垃圾填埋场新鲜渗滤液的实验研究

采用SBR渐减曝气工艺处理模拟城市生活垃圾填埋场新鲜渗滤液,实验研究了反应器运行条件与出水水质的关系及有机碳的转移规律。研究结果表明新鲜渗滤液经24h曝气处理后,出水COD浓度约为500mg/L,BOD5/COD降为014左右;出水COD浓度与容积负荷无明显相关性;COD去除率与容积负荷呈正比,并在容积负荷为50kgCOD/m3·d时达到最高,约95%;去除的有机碳气相转化率与容积负荷呈正比,在容积负荷为50kgCOD/m3·d时,有机碳气相转化率接近100%;该系统最高容积负荷为50kgCOD/m3·d,相应的污泥浓度(以混合液悬浮性挥发固体(MLVSS)计)为712g/L。     

准好氧填埋场FSQ标准的室内模拟研究

以室内模拟实验为基础,对准好氧填埋场的FSQ标准作了相关研究.实验结果表明,准好氧填埋的渗滤液COD与其他指标的变化具有明显的不同步性,根据该特点,把准好氧填埋场的稳定化过程划分为不稳定、基本稳定和完全稳定3个阶段.相应把准好氧填埋的FSQ标准分为2级:基本稳定状态时的FSQ二级标准,完全稳定状态时的FSQ一级标准.在评价基本稳定状态时,场地沉降量为控制性指标,确定准好氧填埋的FSQ二级标准为:填埋场地总沉降量占垃圾初始填埋高度的比例≥30%,渗滤液COD≤400 mg/L、NH3-N≤15 mg/L、TVS/TDS≤6%,固相垃圾BDM≤6%;在评价完全稳定状态时,渗滤液COD作为控制性指标,概化总结出准好氧填埋的FSQ一级标准为:填埋场地总沉降量占垃圾初始填埋高度的比例＞30%,渗滤液COD≤100 mg/L、NH3-N≤15mg/L、TVS/TDS≤3%,固相垃圾BDM≤3%.     

垃圾填埋场甲烷氧化菌及甲烷通量的研究

采用静态箱法、滚管计数法和气相色谱法,对6个不同封场时间填埋区的甲烷通量、覆土层甲烷氧化菌数量和甲烷氧化速率的变化趋势进行了测定,并分析了它们与封场时间、植被覆盖率等因素之间的相关性。结果发现6个填埋区甲烷通量的变化范围在-0.34～5.31 mg/(m2.h)之间;覆土层甲烷氧化菌的数量范围为3.10×107～20.77×107 cfu/g干土,甲烷氧化速率在1.65×10-8～4.34×10-8mol/(h.g)之间。覆土层甲烷氧化菌的数量与甲烷氧化速率呈正相关,但前者并不是后者的决定性因素;甲烷通量高时可刺激甲烷氧化菌数量及氧化速率的提高,且三者均与封场时间呈显著负相关,与植被覆盖率呈负相关;当含水率大于15%时,随着覆土层含水率的增加,甲烷氧化速率呈下降趋势;覆土pH、有机质和铵态氮与甲烷氧化速率等无明显相关性。提高覆土层的甲烷氧化速率可有效减少垃圾填埋场的甲烷排放。     

Neutralization/prevention of acid rock drainage using mixtures of alkaline by-products and sulfidic mine wastes

Backfilling of open pit with sulfidic waste rock followed by inundation is a common method for reducing sulfide oxidation after mine closure. This approach can be complemented by mixing the waste rock with alkaline materials from pulp and steel mills to increase the system’s neutralization potential. Leachates from 1 m³ tanks containing sulfide-rich (ca.30 wt %) waste rock formed under dry and water saturated conditions under laboratory conditions were characterized and compared to those formed from mixtures. The waste rock leachate produced an acidic leachate (pH?<?2) with high concentrations of As (65 mg/L), Cu (6 mg/L), and Zn (150 mg/L) after 258 days. The leachate from water-saturated waste rock had lower concentrations of As and Cu (<2 μg/L), Pb and Zn (20 μg/L and 5 mg/L), respectively, and its pH was around 6. Crushed (<6 mm) waste rock mixed with different fractions (1–5 wt %) of green liquid dregs, fly ash, mesa lime, and argon oxygen decarburization (AOD) slag was leached on a small scale for 65 day, and showed near-neutral pH values, except for mixtures of waste rock with AOD slag and fly ash (5 % w/w) which were more basic (pH?>?9). The decrease of elemental concentration in the leachate was most pronounced for Pb and Zn, while Al and S were relatively high. Overall, the results obtained were promising and suggest that alkaline by-products could be useful additives for minimizing ARD formation.     

EGSB反应器处理城市生活垃圾沥滤液

采用膨胀颗粒污泥床(EGSB)反应器对城市生活垃圾焚烧厂产生的垃圾沥滤液进行处理。实验结果表明:中温条件下,当COD浓度为55 000 mg/L左右,有机容积负荷(OLR)为22.8 kg COD/(m3.d)时,EGSB对垃圾沥滤液具有较好的的处理效果,COD去除率可达94.2%。当进水COD为72 000 mg/L左右时,为保证反应器的稳定运行,OLR应降低至18.2 kg COD/(m3.d),此时COD去除率可以达到88%左右,出水COD平均为9 103 mg/L。垃圾沥滤液和EGSB处理出水均以小分子量有机物为主,其中<4 kDa的有机物分别占76.5%和74.4%。EGSB对整个分子量区间的溶解性有机物都有较好的处理效果,其中对大分子有机物的处理效率相对更高。     

Methane oxidation in compost-based landfill cover with vegetation during wet and dry conditions in the tropics

The effect of compost and vegetation on methane (CH4) oxidation was investigated during wet and dry conditions in a tropical region. A laboratory-scale experiment was conducted to examine the performance of nonvegetated and vegetated landfill cover systems in terms of CH4 oxidation efficiency. Two types of landfill cover materials (compost and sandy loam) and two species of tropical grasses (Sporobolus virginicus and Panicum repens) were studied for their effect on the CH4 oxidation reaction. It was found that the use of compost as cover material could maintain a high methane oxidation rate (MOR) of 12 mol CH4/m3 x day over a 250-day period. Leachate application showed a positive effect on promoting methanotrophic activity and increasing MOR. A high MOR of 12 mol CH4/m3 x day was achieved when using compost cover with P. repens during wet and dry seasons when leachate irrigation was practiced. In dry conditions, a lower MOR of 8 mol CH4/m3 x day was observed for 80 days.     

高氨氮对厌氧生物法处理城市垃圾渗沥液的影响

研究了高浓度氨氮对厌氧膜生物法处理城市垃圾渗沥液的影响。结果表明,COD去除率、沼气产量、沼气产率、辅酶F420和最大比产甲烷活性均随氨氮浓度的增加而减小;当氨氮浓度<3600mg/L时,不会对厌氧膜生物反应器的运行产生明显的影响;氨氮对厌氧污泥产甲烷活性的50%抑制浓度为4350mg/L;高浓度氨氮会造成系统VFA浓度增加;当氨氮浓度由4800mg/L降低到2000mg/L后,受重度抑制的厌氧微生物的活性可以在20d里恢复到未受抑制时的活性水平。     

高氨氮对厌氧生物法处理城市垃圾渗沥液的影响

研究了高浓度氨氮对厌氧膜生物法处理城市垃圾渗沥液的影响。结果表明，COD去除率、沼气产量、沼气产率、辅酶F420和最大比产甲烷活性均随氨氮浓度的增加而减小；当氨氮浓度〈3600mg/L时，不会对厌氧膜生物反应器的运行产生明显的影响；氨氮对厌氧污泥产甲烷活性的50％抑制浓度为4350mg／L；高浓度氨氮会造成系统VFA浓度增加；当氨氮浓度由4800mg／L降低到2000mg/L后，受重度抑制的厌氧微生物的活性可以在20d里恢复到未受抑制时的活性水平。     

模拟生物反应器加速产甲烷过程研究

渗滤液原液回灌易导致填埋垃圾产甲烷过程的滞后,从而对甲烷收集利用产生不利影响。通过3根实验室模拟生物反应器,研究了原液回灌(C1)、渗滤液好氧预处理后回灌(C2)和原液回灌+垃圾层上部通风曝气(C3)3种填埋方式下的填埋气产气规律。结果表明,C1甲烷浓度经历短暂上升,达到19.5%后开始逐渐降低,产甲烷速率和产甲烷总量均很低;C2甲烷浓度逐渐上升,在第121天时甲烷浓度达到50%,产甲烷最高速率和产甲烷总量分别为0.31 L/(kg·d)和25.2 L/kg。在停止上部垃圾层通风曝气后,C3甲烷浓度迅速上升,在81 d时甲烷浓度便达到50%以上,最大产甲烷速率和产甲烷总量分别为0.22 L/(kg·d)和16.0 L/kg。对各模拟柱填埋气可回收性评价结果表明,C3填埋气可回收利用比例最高,C2略低,C1在实验期间内则无可回收利用气体产生。     

Online oxygen control for sulfide oxidation in anaerobic treatment of high-sulfate wastewater.

A new technique for sulfide control was investigated in an upflow-anaerobic filter (UAF) treating high-strength, sulfate-rich wastewater. The technique used periodic oxygen injection using oxidation-reduction potential (ORP) as a controlling parameter to regulate oxygen injection. The UAF was operated at a constant influent total-organic carbon of 6740 mg/L but with different influent sulfates of 1000, 3000, and 6000 mg/L. At 1000 and 3000 mg/L influent sulfates, the produced sulfide did not impose any inhibition to methane-producing bacteria (MPB). However, at 6000 mg/L influent sulfate, the produced dissolved sulfide of 804 mg S/L (free sulfide = 280 mg S/L) severely inhibited the methanogenesis, but not the sulfidogenesis. Upon oxygen injection at elevated ORP of -265 mV, sulfides were almost completely eliminated with a concomitant improvement in methane yield by 46%. If oxygenation was excessive because of an oversetting of ORP, the excess oxygen could be used rapidly by facultative heterotrophs, thereby protecting the MPB from oxygen stress. Regarding online sulfide oxidation, it was found that the biogas and injected oxygen needed to pass through an aqueous layer containing trace metals, which were found to have a significant catalytic effect on abiotic sulfide oxidation.     

Polyfluoroalkyl compounds in landfill leachates

Polyfluoroalkyl compounds (PFCs) are widely used in industry and consumer products. These products could end up finally in landfills where their leachates are a potential source for PFCs into the aqueous environment. In this study, samples of untreated and treated leachate from 22 landfill sites in Germany were analysed for 43 PFCs. ΣPFC concentrations ranged from 31 to 12,819 ng/L in untreated leachate and 4-8060 ng/L in treated leachate. The dominating compounds in untreated leachate were perfluorobutanoic acid (PFBA) (mean contribution 27%) and perfluorobutane sulfonate (PFBS) (24%). The discharge of PFCs into the aqueous environment depended on the cleaning treatment systems. Membrane treatments (reverse osmosis and nanofiltrations) and activated carbon released lower concentrations of PFCs into the environment than cleaning systems using wet air oxidation or only biological treatment. The mass flows of ∑PFCs into the aqueous environment ranged between 0.08 and 956 mg/day.