UASB-生物接触氧化-絮凝沉淀法处理皂素废水

采用UASB-生物接触氧化—絮凝沉淀处理高浓度皂素生产度水,试验结果表明,UASB厌氧反应器COD去除率在80%以上,生物接触氧化COD去除率在60%以上,絮凝沉淀COD去除率在60%以上。     

干扰素生产废水处理试验及生物相分析

采用水解酸化与生物接触氧化组合工艺对干扰素生产废水进行试验研究,并考察其处理效果,观察生物接触氧化工艺中生物相。结果表明：该组合工艺对出水COD的去除率大于90%,出水COD低于40 mg/L,且运行稳定后生物接触氧化槽中污泥浓度较低。对生物相的显微镜观察可知生物接触氧化槽中生物相种类以藻类为主。     

光伏产业清洗剂废水低温生物处理

光伏产业清洗剂废水冬季生物处理难稳定达标.操作参数调控与工艺的优化组合对微生物活性的提高及清洗剂废水稳定达标处理的实现具有重要意义.本研究通过实验室摇瓶试验以COD(Chemical Oxygen Demand)去除率、COD去除速率等为表征指标探究不同温度以及低温下p H、C/N(COD/NH_4~+-N)及处理工艺等对该废水生物处理效果的影响.结果显示,10℃下清洗剂废水生物处理效果受到明显抑制,21.5 h时COD去除率仅为49.7%,较30℃下降31.0%;偏碱性条件更利于该废水的处理.p H 8条件下COD去除率较p H为5.5时提高57.2%;初始C/N在8:1到32:1之间更利于该废水的处理.清洗剂废水在生物处理后期均出现降解停滞现象.进一步比较不同工艺下清洗剂废水的低温(15℃)处理效果,在15℃、p H 7-8和C/N 16:1条件下,相比活性污泥法,接触氧化法可将COD去除率提高7.5%左右;而两段式接触氧化法可将第二段处理中的COD去除率提高16.6%左右,最终出水达到污水综合排放标准(GB 8978-1996)中的一级标准.本研究通过两段式接触氧化实现了清洗剂废水的有效处理,但是该废水的降解动力学及两段式接触氧化体系中的微生物低温降解机理还有待进一步的研究和验证.(图4表3参19)     

甲醇工业废水处理回用作循环冷却水研究

首次采用(A1/O1)/(A2/O2)厌氧水解酸化—膜微孔曝气生物接触氧化/缺氧生物接触氧化—膜微孔曝气生物接触氧化塔—混凝沉淀—活性炭过滤—二氧化氯消毒处理工艺集成系统处理含甲醇工业废水。在进水后先设厌氧水解调节池以大幅提高废水可生化性,再用膜微孔曝气生物接触氧化好氧处理去除废水中大部分COD。然后用兼氧细菌接种缺氧处理去除废水中部分COD,并提高废水的可生化性。再用好氧内循环曝气生物塔处理去除废水中剩余的COD。处理工艺系统以生物降解有机物为主,后设配套的活性炭深度处理工艺,以确保整个处理工艺出水满足要求。在原水水质为含甲醇0.03%～5%(质量分数,下同),pH6～10,SS为30～100mg·L-1,CODcr为200～500mg·L-1条件下,处理系统出水达到冷却塔循环用水标准和要求,满足工业循环冷却水的需要。     

混凝沉淀-两段接触氧化法处理制革废水工程实践

采用混凝沉淀-两段接触氧化法处理制革区综合制革废水,经过半年多稳定运行,系统COD去除率达到96%,硫化物去除率达到99.5%,处理后出水的各项指标完全达到了国家《污水综合排放标准》(GB8978-1996)制革行业废水二级标准。对废水处理系统的工艺作了简单介绍,对系统调试、运行结果进行了分析与总结。     

加压生物接触氧化法处理染料废水

本试验用一种新方法——加压生物接触氧化法处理染料生产废水.试验规模为1m~3/h.废水先经调节预处理,进水水质平均COD为619mg/L,BOD_5为336mg/L时,经6.5h处理后,出水COD去除率可达70%,BOD_5去除率在98%以上.与常规法相比,它具有处理时间短,主要设备占地面积小,设备投资省及操作总能耗低的特点.     

内电解-混凝组合技术对合成制药废水的预处理

采用多级内电解反应器与混凝沉淀组合技术预处理典型合成制药废水.研究结果表明,组合技术对制药废水的COD去除率高于单一混凝技术和单一内电解技术;以PAM作为混凝剂的处理效果优于Ca（OH）2,在PAM投加浓度为10 m.gL-1,pH值为8的条件下,内电解与混凝沉淀组合技术对制药废水COD的去除率可达到30%.同时,组合...     

亚洲玉米螟性信息素合成废水的处理方法

本文研究了一种新型消灭农作物害虫的药物——亚洲玉米螟性信息素在合成过程中排放的废水的处理方法。经混凝沉降—氧化—活性碳吸附三级处理后,废水的COD值下降77.1％、有机磷去除率达90％以上、硫化物去除率达90％以上,恶臭基本消除。     

废水处理生物出水中COD构成的解析——以焦化废水为例

以焦化废水为例,采用连续过滤及化学分析的方法考察了悬浮组分、胶体组分及溶解组分对生物出水残余COD的贡献,并结合紫外-可见光谱和GC/MS图谱定性解析各形态组分的有机构成特征,构建了一种废水生物出水COD构成解析的评价方法.实验结果显示,焦化废水生物处理出水中悬浮态和胶体态组分对残余COD的贡献分别占COD总量的25.9%—46.3%和18.7%—44.4%,建议优先考虑采用混凝沉淀工艺去除约35.0%—45.0%的COD,使处理出水基本能够达标排放;溶解组分的COD占COD总量的24.6%—40.7%,其中4.3%—15.8%的COD由硫化物、硫氰化物等还原性物质贡献,其余部分主要由链状烃类、酯类及醇类等溶解有机组分贡献,建议采用氧化或吸附工艺进行处理,以满足更高的出水水质要求.     

ZnO-MgO/Al2O3吸附-臭氧催化氧化处理难降解有机废水

以活性氧化铝为载体,采用浸渍法制备催化剂,对甲基橙及草酸模拟废水进行处理.在中性条件下,臭氧催化氧化比单独臭氧氧化能提前30 min使得甲基橙溶液褪色,反应105 min时,臭氧催化氧化对TOC的去除率高达96.53%,比单独使用臭氧氧化对甲基橙TOC去除率提高了47.19%,在处理草酸废水时臭氧催化氧化对TOC去除率高达80.59%,比单独使用臭氧氧化对草酸TOC去除率提高了59.14%.在处理甲基橙及草酸的小试实验中催化剂对有机污染物的吸附作用起到了加快反应进行的作用.在对垃圾渗滤液超滤出水时,O₃与COD质量比为1:1时,臭氧催化氧化对COD去除率为49.09%,比单独使用臭氧氧化提高36.37%,臭氧催化氧化对TOC的去除率是单独使用臭氧氧化的2.54倍,在处理垃圾渗滤液纳滤浓水时,臭氧催化氧化对COD去除率高达88.72%,比单独使用臭氧氧化提高37.60%,并且臭氧催化氧化对TOC的去除率是单独臭氧氧化的1.6倍.臭氧催化氧化反应过程中产生的羟基自由基对有机物更快的反应速率.     

二段生物接触氧化法处理含硫废水的中试研究

用二段生物接触氧化法探索炼油过程中所产生的含硫废水的处理新方法． 结果表明：经此工艺处理后的出水 Ｃ Ｏ Ｄ、氨氮、硫化物和酚的质量浓度ρ分别为２６６ ．９ ｍｇ／ Ｌ、８２ ．８５ ｍｇ／ Ｌ、１ ．１８ ｍｇ／ Ｌ 和１ ．４３ ｍｇ／ Ｌ,相应的去除率分别为８６ ．３ ％ 、４０ ％ 、９２ ．７ ％ 和９９ ．３ ％ ,出水水质达到国家三级排放标准． 进出水水质的变化曲线表明,生物接触氧化法处理含硫废水对进水水质变化的适应能力比较强,出水水质比较稳定,显示了二段接触氧化法处理含硫废水的可行性     

垃圾填埋渗滤液的处理方法

不同的垃圾填埋场及其对出水水质的不同要求,采用的处理方法也不尽相同。本文针对渗滤液的特点及出水情况,介绍了几跑步同的垃圾渗滤的处理方法,包括生物化学方法和深度氧化方法。     

生物快滤池深度处理城市污水的性能及pH值变化规律

采用生物快滤池对城市污水厂二级出水进行深度处理的试验表明,生物快滤池对进水水质变化有很大的适应性,除卫生学指标外,其它指标出水绝大部分时间可满足生活杂用水水质标准(CJ25.1-89)中的洗车标准。随着进水水质的不同,生物快滤池中生化反应类型也随之变化,相应地滤池出水pH值也有不同的变化规律。可以通过生物快滤池进出水pH值的变化情况来判断滤池内生化反应类型和COD或氨氮指标的去除效果。     

Fenton——聚硅铝铁处理生活垃圾压滤液研究

为了降低生活垃圾压滤液污染负荷,为后续生化处理的正常运行创造良好条件,针对垃圾压滤液污染特性,以CODCr去除率为指标,通过正交实验和单因素实验研究了Fenton—聚硅铝铁混凝法处理城市生活垃圾压滤液的最优反应条件和处理效果。结果表明:采用该工艺处理垃圾压滤液时,pH值对CODCr去除率影响最大,其次是PSAF,再次是H2O2和FeSO4,在最优反应条件下,浊度去除率达到95.3%,CODCr去除率达到86.7%,BOD5去除率达到81.6%,浊度、CODCr、BOD5分别下降到86NTU、4201 mg.L-1、855 mg.L-1。     

Comparison of membrane fouling in ultrafiltration of down-flow and up-flow biological activated carbon effluents

The UF membrane fouling by down- and up-flow BAC effluents were compared. Up-flow BAC effluent fouled the membrane faster than down-flow BAC effluent. The combined effects dominated irreversible fouling. The extent of fouling exacerbated by inorganic particles was higher. The TMP, permeate flux, and normalized membrane flux during 21 days of UF of DBAC and UBAC effluents. Fouling during ultrafiltration of down- and up-flow biological activated carbon effluents was investigated to determine the roles of polysaccharides, proteins, and inorganic particles in ultrafiltration membrane fouling. During ultrafiltration of down- flow biological activated carbon effluent, the trans-membrane pressure was≤26 kPa and the permeate flux was steady at 46.7 L?m⁻²?h⁻¹. However, during ultrafiltration of up-flow biological activated carbon effluent, the highest trans-membrane pressure was almost 40 kPa and the permeate flux continuously decreased to 30 L?m⁻²?h⁻¹. At the end of the filtration period, the normalized membrane fluxes were 0.88 and 0.62 for down- and up-flow biological activated carbon effluents, respectively. The membrane removed the turbidity and polysaccharides content by 47.4% and 30.2% in down- flow biological activated effluent and 82.5% and 22.4% in up-flow biological activated carbon effluent, respectively, but retained few proteins. The retention of polysaccharides was higher on the membrane that filtered the down- flow biological activated effluent compared with that on the membrane that filtered the up-flow biological activated carbon effluent. The polysaccharides on the membranes fouled by up-flow biological activated carbon and down- flow biological activated effluents were spread continuously and clustered, respectively. These demonstrated that the up-flow biological activated carbon effluent fouled the membrane faster. Membrane fouling was associated with a portion of the polysaccharides (not the proteins) and inorganic particles in the feed water. When there was little difference in the polysaccharide concentrations between the feed waters, the fouling extent was exacerbated more by inorganic particles than by polysaccharides.     

Mechanisms for simultaneous ozonation of sulfamethoxazole and natural organic matters in secondary effluent from sewage treatment plant

• SMX was mainly degraded by hydrolysis, isoxazole oxidation and double-bond addition. • Isoxazole oxidation and bond addition products were formed by direct ozonation. • Hydroxylated products were produced by indirect oxidation. • NOM mainly affected the degradation of SMX by consuming ^•OH rather than O₃. • Inhibitory effect of NOM on SMX removal was related to the components’ aromaticity. Sulfamethoxazole (SMX) is commonly detected in wastewater and cannot be completely decomposed during conventional treatment processes. Ozone (O₃) is often used in water treatment. This study explored the influence of natural organic matters (NOM) in secondary effluent of a sewage treatment plant on the ozonation pathways of SMX. The changes in NOM components during ozonation were also analyzed. SMX was primarily degraded by hydrolysis, isoxazole-ring opening, and double-bond addition, whereas hydroxylation was not the principal route given the low maximum abundances of the hydroxylated products, with m/z of 269 and 287. The hydroxylation process occurred mainly through indirect oxidation because the maximum abundances of the products reduced by about 70% after the radical quencher was added, whereas isoxazole-ring opening and double-bond addition processes mainly depended on direct oxidation, which was unaffected by the quencher. NOM mainly affected the degradation of micropollutants by consuming ^•OH rather than O₃ molecules, resulting in the 63%–85% decrease in indirect oxidation products. The NOM in the effluent were also degraded simultaneously during ozonation, and the components with larger aromaticity were more likely degraded through direct oxidation. The dependences of the three main components of NOM in the effluent on indirect oxidation followed the sequence: humic-like substances>fluvic-like substances>protein-like substances. This study reveals the ozonation mechanism of SMX in secondary effluent and provides a theoretical basis for the control of SMX and its degradation products in actual water treatment.     

物化预处理-水解酸化-接触氧化法处理选矿废水

对某浮选厂浮选废水进行混凝沉淀+活性碳吸附预处理,然后进入生化系统,厌氧池、好氧池停留时间为10h.结果证明:进水COD为400～700mg/L,出水74～145 mg/L,去除率达75.8%以上,首次成功地将生物法应用到铅锌选矿废水的处理,若对该工艺进行适当调整,完全可以使出水达到排放或回用标准.     

Photo detoxification of solubilized vat dye effluent using different pH ranges

The removal of solubilized vat dye effluent using photo detoxification method was studied at various pH ranges. Experiments were carried out with synthetic effluent using total dye concentrations of 50, 100, 200, 300, and 350 mg/L. In sunlight photo oxidation, the original soluble vat dye is precipitated and can be filtered and reused by the textile industries. The effect of the different concentrations (1,000, 2,000, 3,000 mg/L) of total dissolved solids on the removal of vat dye was also carried out in the photo detoxification process. The efficiency of the dye removal was found to be 99 %.