超声-双氧水和亚铁离子体系处理含酚废水研究

在实验装置上对超声-双氧水和亚铁离子体系联合处理含酚废水进行了实验研究。主要考察了废水初始pH值、初始双氧水浓度、超声功率、反应时间等因素对酚去除率的影响。实验结果表明：超声辐射可以在双氧水和亚铁离子体系氧化过程中起加速反应的作用，而且随着超声功率的增大，加速反应的能力增强；实验条件下废水初始pH值为4～6．8，初始双氧水浓度为140mg／L时酚去除效果最佳；超声-双氧水和亚铁离子体系处理含酚废水过程中苯酚的降解规律符合表现一级反应。     

臭氧氧化法处理高浓度苯酚废水

采用臭氧氧化技术对高浓度含酚废水进行了研究.考察了臭氧进气量、反应时间、温度及溶液初始pH值等因素对苯酚COD的去除率的影响.研究表明:在一定范围内,随臭氧进气量的增加、反应时间的增长,COD去除率增大;温度对COD去除率的影响不大;溶液的初始pH值对臭氧氧化有比较重要的影响,在pH值为11～12左右时,COD的去除率最大;在臭氧氧化处理高浓度含酚废水的过程中,酚的降解规律符合表观一级反应.     

纳米二氧化钛光催化氧化降解苯酚废水实验

开展实验室模拟苯酚废水的二氧化钛光催化氧化实验。结果表明：在苯酚废水曝气量为0～3L/min的条件下,随着曝气量的增大,COD去除率先增大后减小;初始浓度不变,光照时间为1h的条件下, 调节pH值在3～11,苯酚废水COD去除率随着pH值的增大而减小,当pH值为11时, COD去除率又开始增 大,酸性条件比碱性条件下COD去除率高;随着二氧化钛投加量的增加,COD去除率增大,当二氧化钛投加量 为10g/L时,COD去除率反而降低,二氧化钛最佳投加量为3g/L;随着苯酚废水初始浓度由75mg/L增加至300mg/L,COD去除率由78.2％降低到58.1％;反应温度的改变对COD和TOC的去除率没有影响。     

Fenton氧化处理微电解后制浆中段废水的研究

对微电解后废水初始pH、外加Fe2+、H2O2浓度、处理时间对色度及CODCr去除率的影响进行研究。实验结果表明随着pH的增加,色度和CODCr的去除率均呈现先增加后降低的趋势,在pH值等于4时,处理效果最好。外加Fe2+,H2O2和反应时间对废水CODCr和色度去除率的影响类似于pH的影响,获得的H2O2最佳投加量4 mL/L,FeSO4.7H2O为1.5g/L,最佳处理时间60min。在优化实验条件下,CODCr和色度的去除率稳定在80%和84%附近。     

三维电极催化氧化技术深度处理垃圾渗滤液

以“A/O-MBR”工艺生化处理后的垃圾渗滤液为研究对象,采用三维电极催化氧化技术深度处理垃圾渗滤液。实验研究了反应时间、电流密度、曝气量、反应初始pH对渗滤液深度处理效果的影响。研究结果表明,三维电极催化氧化技术深度处理垃圾渗滤液的最佳工艺参数为：反应时间60 min,电流密度15 mA/cm2,曝气量500 m L/min,初始pH=5.0。在最佳工艺参数下连续进行渗滤液废水深度处理,实验系统在进水COD均值935 mg/L的情况下,处理出水COD均值201 mg/L,系统运行稳定性较好,COD平均去除率达到78.50%。     

催化氧化法在钻井废水处理中的应用

在油气田深井钻探过程中产生的钻井液,经固-液分离处理后产生的废水具有化学需氧量高、色度高、矿化度高、含油量高等特点,须进一步进行处理。采用Fenton试剂对钻井废水进行了催化氧化处理实验。结果表明,处理后, 废水中化学需氧量(COD)去除率可达82%,色度去除率为98.5%。H2O2/Fe2+投量摩尔比、H2O2/初始COD摩尔比、pH值和反应时间对废水COD、色度的去除率均有较大影响。用Fenton试剂催化氧化工艺处理聚磺体系钻井废水还具有处理效率高、操作简便、适用范围广等优点。     

焙烧水滑石去除水中硝酸盐的实验研究

利用层状双氢氧化物的结构记忆效应,探讨了焙烧水滑石处理模拟含硝酸盐废水的可行性,考察了pH值、温度、反应时间、振荡速度等因素对硝酸盐去除率的影响。结果表明,当pH为9、反应温度298K、吸附时间120min、LDO投加量0.1g/100ml时,硝酸盐氮初始浓度为100mg/L;震荡速度为150r/min时,总氮的去除率高达96.73%。焙烧水滑石对硝酸盐的吸附符合Freudlich等温方程。     

超声内电解处理高浓度含盐有机废水的实验研究

分别研究了铁碳内电解、超声波辐照以及不同组合方式对高盐度泡菜废水的处理,重点研究了铁碳比、铁碳加入量、溶液pH值、处理时间、超声功率密度等因素对高含盐量泡菜废水降解率的影响。实验表明,铁碳加入对内电解处理效果影响显著,超声波处理该废水的最佳pH值为7;超声内电解处理的最佳条件为：铁碳比2∶1,铁碳加入体积为溶液体积的25%,溶液初始pH值为7,超声功率密度为0.225w/cm3,曝气处理90min。处理后出水COD去除率大于50%,达到了对该类高浓度含盐废水的预处理效果,降低了后续生化系统的处理负荷。     

臭氧高级氧化法处理染料废水的研究

采用臭氧高级氧化技术对某染料废水进行处理,探究不同条件对染料废水COD以及色度的去除效果的影响,确定最佳工艺条件。在最佳条件下,采用单独臭氧、单独紫外、臭氧-紫外、臭氧-双氧水以及臭氧-铁炭五种氧化方法对染料废水进行处理。结果表明:臭氧氧化技术最佳条件为pH值=8,臭氧流量80 L/h,反应时间为2 h;采用最佳处理方案,采用臭氧-紫外高级氧化技术处理染料废水,其脱色率为98.3%,COD去除率为67.0%。     

非均相催化臭氧化处理钻井废水的研究

以油田钻井废水为处理对象,采用基于臭氧的非均相催化氧化处理工艺,负载了MnO_2催化剂强化臭氧处理效果,实验对比分析单独臭氧化和非均相催化臭氧化的处理效果差异,确定最佳工艺参数条件。X射线衍射分析表明,过量浸渍法制备的催化剂中含有大量活性组分MnO_2,使非均相催化臭氧化去除钻井废水COD的效率提高了45.8%。经工艺优化后,确定非均相催化臭氧化处理钻井废水最佳条件为:催化剂加量50mg/L、反应pH值为11、反应温度20℃、臭氧浓度85mg/L、处理时间50min,此时废水COD最大去除率为83.1%。通过5次重复实验验证,催化剂和系统稳定性几乎不受影响,出水均达到GB 8978—1996《污水综合排放标准》一级标准。     

Fenton试剂与改性凹凸棒石联合处理微污染水中苯酚的实验研究

研究了Fenton试剂联合聚二甲基二烯丙基氯化铵（PDMDAAC）改性凹凸棒石对模拟微污染水中苯酚的去除效果。考察了pH值、反应时间、投加量、温度等因素对苯酚去除效果的影响。结果表明：先采用Fenton试剂氧化再用改性凹凸棒石吸附对微污染水中苯酚具有较好的去除效果,在pH=9、温度为25℃、改性凹凸棒石投加量为5g／L、吸附时间20min的条件下,苯酚去除率达98．2％。     

光化学氧化法对阴离子表面活性剂降解的初步研究

本试验采用UV/H2O2光氧化法处理含有较高浓度阴离子表面活性剂（LAS）的模拟废水，研究了H2O2投加量、pH值、光照时间、紫外灯光强对LAS降解率的影响。     

二维与三维电解法处理含铜废水的试验研究

以含铜废水为处理对象,考察了二维电解法的电解电压、电解时间、pH值、极间距对铜去除率的影响。在此基础上为提高处理效率,两极间填充活性炭和玻璃珠形成三维电解,确定了三维电解的最佳运行条件是极间距4cm,pH值3～4,电解电压22 V,电解135min,铜离子的去除率为80.6%。     

臭氧氧化法处理印染废水

本实验通过印染废水处理装置的建立,研究了臭氧处理印染废水的消耗量与废水ＣＯＤ值变化、废水色度去除率的关系,,以及不同ｐＨ值的印染废水和臭氧处理时间的关系。实验结果表明：经过处理后废水的ＣＯＤ却除率为３３９％,色度去除率为９９９％。     

Phenol removal from aqueous environments by natural & chemically modified kaolin clay

Natural, acid and base modified kaolin clays were studied for the sake of phenol and 4-chlorophenol removal from aqueous environments and their application to real ground and industrial wastewater samples. Scanning electron microscope (SEM), infrared spectroscopy (IR), X-ray diffraction (XRD), Thermo Gravimetric Analysis (TGA), Differential Thermal Analysis (DTA), and Surface area analysis were employed for characterization of the adsorbents microstructure. Operating factors such as adsorbent dose, solution pH, initial phenol concentration, and contact time were studied. The experimental data displayed that the increase of the adsorbent dose, contact time, and pH value from 2 to 7 increases the efficiency of the removal process. Optimal conditions for phenolic removal were; contact time of 300 min, primary phenol solution of 25 mg/L, pH 7 and 2.5 g/L as an appropriate adsorbent dose using crude (natural), acid modified and base modified kaolin clays. The higher phenolic removal efficiencies were obtained at 5 mg/L as 90, 97, 96.2%, respectively, for the adsorbents in the previously mentioned order. The adsorption capacity in the removal of phenol and 4-chlorophenol were 7.481 and 4.195, 8.2942 and 3.211, and 8.05185 and 18.565 mg/g, respectively, for the adsorbents in the same mentioned order. The adsorption equilibrium data were fitted and analyzed with four isotherm models, namely, Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich isotherm equations. The adsorption process of phenol on studied adsorbents was exothermic, spontaneous and thermodynamically favorable proved by the negative values of their thermodynamic parameters ΔH° and ΔG°. The correlation coefficient (R²) for all concentrations was higher than 0.94, which indicates that in the studied system, the data suitably fit the first-order kinetics. The % desorption capacity was amounted to 96%, 91.11%, and 87.06% of adsorbed phenol, respectively, for the adsorbents in the previous order using 0.1N NaOH and 10% V/V ethanol solutions as eluents at 25°C, indicating the reusability of the adsorbents. Kaolin and its modified forms can be introduced as eco-friendly and low-cost adsorbents in water remediation implementation.     

Combined chemical and biological oxidation of penicillin formulation effluent

Antibiotic formulation effluent is well known for its important contribution to environmental pollution due to its fluctuating and recalcitrant nature. In the present study, the chemical treatability of penicillin formulation effluent (average filtered COD(o)=830 mg/l; average soluble COD(o)=615 mg/l; pH(o)=6.9) bearing the active substances penicillin Amoxicillin Trihydrate (C(16)H(19)N(3)O(5)S.3H(2)O) and the beta-lactamase inhibitor Potassium Clavulanate (C(8)H(8)KNO(5)) has been investigated. For this purpose, the penicillin formulation effluent was subjected to ozonation (applied ozone dose=2500 mg/(lxh)) at varying pH (2.5-12.0) and O(3)+H(2)O(2) (perozonation) at different initial H(2)O(2) concentrations (=2-40 mM) and pH 10.5. According to the experimental results, the overall Chemical Oxygen Demand (COD) removal efficiency varied between 10 and 56% for ozonation and 30% (no H(2)O(2)) and 83% (20 mM H(2)O(2)) for the O(3)+H(2)O(2) process. The addition of H(2)O(2) improved the COD removal rates considerably even at the lowest studied H(2)O(2) concentration. An optimum H(2)O(2) concentration of 20 mM existed at which the highest COD removal efficiency and abatement kinetics were obtained. The ozone absorption rate ranged between 53% (ozonation) and 68% (perozonation). An ozone input of 800 mg/l in 20 min was sufficient to achieve the highest BOD(5)/COD (biodegradability) ratio (=0.45) and BOD(5) value (109 mg/l) for the pre-treated penicillin formulation effluent. After the establishment of optimum ozonation and perozonation conditions, mixtures of synthetic domestic wastewater+raw, ozonated and perozonated penicillin formulation effluent were subjected to biological activated sludge treatment at a food-to-microorganisms (F/M) ratio of 0.23 mg COD/(mg MLSSxd), using a consortium of acclimated microorganisms. COD removal efficiencies of the activated sludge process were 71, 81 and 72% for pharmaceutical wastewater containing synthetic domestic wastewater mixed with either raw, ozonated or perozonated formulation effluent, respectively. The ultimate COD value obtained after 24-h biotreatment of the synthetic domestic wastewater+pre-ozonated formulation effluent mixture was around 100 mg/l instead of 180 mg/l which was the final COD obtained for the wastewater mixture containing raw formulation effluent, indicating that pre-ozonation at least partially removed the non-biodegradable COD fraction of the formulation effluent.     

生物法处理含酚废水的研究

为了降低炼油厂污水处理场的酚负荷,对催化裂化汽提塔所排含酚废水的预处理进行了研究。进行了煤渣吸附实验,酚的生物降解动力学实验及酚在兼氧条件下的处理实验;采用４－氨基安替比林光度法测定酚浓度。实验结果表明采用煤渣填料－生物膜反应器,酚的去除率可达９０％,酚的生物降解符合一级反应动力学,酚类物质可在兼氧条件下降解     

Ultrasound and enzyme assisted biodegradation of distillery wastewater

Irradiation with ultrasound (US) and use of an enzyme (E) as pretreatment techniques were carried out to treat a complex effluent (distillery wastewater). These two techniques have been used alone as well as in combination and the efficacy of these techniques was tested by subjecting the effluent to subsequent aerobic biological oxidation (AO). When used alone, US exposure for 30 min and 2 h yielded the best COD reduction during the aerobic oxidation step (US+AO). For the enzyme when used alone, a pH value of 4.8 (corresponding to the optimum pH of the enzyme), a dose of 50 U and a pretreatment time of 24 h yielded better COD removal efficiency as compared to untreated effluent (aerobic oxidation alone). When used in combination, ultrasound followed by enzymatic pretreatment (US+E+AO) yielded the best COD removal efficiencies during aerobic oxidation as compared to the other combinations tested for the treatment of the distillery wastewater. A 4-fold increase in the initial oxidation rate was observed over the untreated batch for the integrated technique (US+E+AO). On the basis of the variation in the values of the biokinetic parameters it can be concluded that the type of pretreatment scheme affects the subsequent rate of the aerobic oxidation significantly.     

高压电化学絮凝技术去除酿酒废水中总磷的研究

为了使酿酒废水中总磷有效去除并达标排放,通过对酿酒废水总磷的排放情况调查,有针对性的选用高压电化学絮凝技术,对酿酒废水中总磷的去除效果进行实验研究。从实验结果看,调节进水pH值为2.3、停留时间45分钟时总磷去除率可达到99%以上,在该条件下COD的去除率也能达到50%左右,废水总磷排放浓度能够达到1.0mg/L的排放要求。