刚毛藻对Cu、Fe、Zn的耐受与污染控制研究

研究刚毛藻对Cu、Fe、Zn的耐受情况。实验设计了3种重金属的浓度,分别为00、.5 mg/L1、.0 mg/L、2.5 mg/L、5.0 mg/L、7.5mg/L1、0 mg/L的培养液,培养期间观察记录刚毛藻的长势,测定藻类生物量及叶绿素a的含量变化,研究藻体对模拟水中3种重金属的去除动态及实际去除效果。结果表明,3种重金属在低浓度(0.5—2.5 mg/L)时藻体长势较好;浓度达到5mg/L时开始出现毒害现象,表现为叶绿素a含量下降趋势;浓度达到7.5mg/L以上时藻体死亡。水体中有效Cu、Fe、Zn浓度较低时,藻体对3种重金属去除效果较好,较高浓度时由于毒害作用使其对3种重金属的去除能力下降。     

高锰酸钾预氧化强化微污染水源水中锰的去除

目前,我国很多地区地表水都存在锰超标问题,这给供水安全带来了极大隐患.本文考察了高锰酸盐预氧化强化水中锰的去除效果.实验结果表明,原水经过高锰酸盐处理后,水中的锰含量明显降低,当高锰酸盐投加量达到0.5mg/L之后,水中的锰离子浓度已经达到了原子吸收检出限以下,但色度有所增加.当高锰酸钾∶硫酸亚铁=1∶4时,水中的锰去除效果较好,色度降低,随着亚铁离子投加比例的增加,水中锰的去除率反而下降.     

煤层气采出水达标排放处理技术研究

以鄂东区块采出水为研究对象,在对其水质特征充分分析的基础上,研究提出了“固定化微生物”曝气生物滤池的采出水COD和NH3-N的去除工艺,开展了3个阶段的现场试验进行COD和NH3-N去除效果的验证,同时采用GC-MS分析方法探究采出水中有机物氧化降解情况。试验数据显示：最终出水的COD、NH3-N均低于40,2mg/L排放指标要求,难降解有机物种类和数量大幅减少。其中,COD去除率从70％逐步提升至880％,且随水力停留时间（HRT）增加而不断提升;NH3-N去除率可稳定达到99％以上,远低于标准设定值2mg/L,且对HRT的调整不敏感。研究结果表明,以“固定化微生物-曝气生物滤池＋活性炭吸附”为主体的工艺的处理技术,对鄂东区块采出水中的COD,NH3-N和难降解有机物均具有明显的去除效果,将HRT调整至8h左右时,出水仍可稳定达标,此时的直接运行费用将降至1.40元/m3以下,较化学处理工艺处理费用低70％以上,实现了鄂东区块煤层气采出水的“低成本、 稳定达标排放”处理。     

双滤料曝气生物滤池污水深度处理的研究

采用陶粒、沸石为滤料的曝气生物滤池对生物处理系统二级出水进行深度处理回用,研究了水力停留时间、气水体积比对污染物COD和NH3-N处理效果的影响。结果表明：水力停留时间为8 h,气水体积比为3∶1的工况下,处理效果较好。稳定运行后,出水COD、BOD5、SS、NH3-N、TP和色度平均值分别为15.6 mg/L、3.2 mg/L、8.5 mg/L、1.24 mg/L、0.40mg/L和8度,达到《城市污水再生利用—城市杂用水水质》（GB/T 18920-2002）标准,出水可用于道路清扫、绿化等。     

强碱三元复合驱采出水处理工艺技术研究

常规的"沉降+过滤"方式用于三元复合驱采出水处理,聚合物或黏度对石油类和SS的高效去除有较大影响,处理思路应以脱稳降黏为主。文章探索了采用的"气浮沉降+生化氧化+高级氧化+二级过滤"工艺,达到石油类≤800 mg/L,SS≤350 mg/L,黏度≤12 mPa·s,PAM≤800 mg/L,使采出水处理稳定达到回注水要求,降低滤池冲洗难度,降低了固液分离难度,提高了工艺运行稳定性。对于采出水进一步开展膜深度处理,采出水实现回注低渗透层等具有重要意义。     

含硝基苯、苯胺废水处理的工程实践

采用固定化微生物-曝气生物滤池与铁-炭微电解法联用的工艺方法处理含硝基苯、苯胺的废水。通过培养驯化微生物阶段、半负荷进水阶段、满负荷进水阶段的调试运行,表明:当进水CODCr<1 000mg/L、硝基苯<120mg/L、苯胺<30mg/L时,出水可达到CODCr<300mg/L、硝基苯<5mg/L、苯胺<5mg/L的设计要求。铁-炭微电解法在pH值为3～4时,对废水有一定的脱色作用,但pH值升高后脱色效果不明显。     

高海拔寒冷地区污水处理厂地表水准Ⅳ类改造工程研究

为提高西部某污水厂出水水质达到地表水准Ⅳ类标准,对该水厂进行工程改造及优化运行。通过采用投加耐冷微生物、好氧池投加填料,改造微生物膜——活性污泥复合工艺,以及调试运行参数以及间歇曝气等措施观察COD、氨氮、TN和TP去除效果的变化,最后辅以高效混凝沉淀池保证出水达标。实验结果表明:好氧池末端DO降到1mg/L时,出水TN浓度减少到17.57mg/L,TP浓度减少到0.48mg/L,氨氮和COD仍去除稳定;TN去除效果随着分点进水量增加而提高,出水TN平均浓度降到14.13mg/L;污泥回流比由100%减少到60%,TN去除率提高,出水TN平均浓度降到13.14mg/L;通过将好氧区改为间歇曝气后,氨氧化菌和反硝化除磷菌成为优势菌种,加强了氮磷的去除,出水TN、TP浓度分别为11.80mg/L和0.35mg/L,TP仍需。经过优化运行后出水水质稳定达到要求,并有效的解决了氧化沟反应池内溶解氧盈余、污泥浓度控制等问题,同时起到很好的节能降耗效果。     

H2O2／Fe^2＋氧化偶合混凝法处理干膜废水的研究

本文研究了H2O2／Fe^2＋氧化偶合混凝法处理印刷电路板厂干膜废水。讨论了包括过氧化氢浓度、亚铁离子浓度、pH值、时间和混凝pH值等影响因素,试验结果表明,当过氧化氢浓度为457.0mg/L、铁离子浓度为400mg/L、氧化pH值4.0、反温度为40℃、反应时间180min时,COD去除率达84.7%,出水的水质达到排放标准。     

O3/H2O2工艺去除脱硫废水中COD的性能研究

O₃/H₂O₂高级氧化技术具有氧化能力强和无选择性等优点,被广泛用于高浓度、难降解和有毒有害的有机废水处理。考察了O₃/H₂O₂工艺在不同条件(H₂O₂投加量、pH、反应时间)下对脱硫废水中COD去除的影响。结果表明：H₂O₂为0.02 mg/L时去除效果最好,但随着用量的增加,效果逐渐变差;当废水pH为12时COD去除效果最好;当反应时间为1 min时,可达到COD低于90 mg/L的效果。     

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。     

Treatment of wastewater phosphate by reductive dissolution of iron: use of ferric oxyhydroxide media

In smaller wastewater treatment systems such as septic systems, there is an interest in the development of passive phosphorus (P) removal methods. This study tested fixed-bed filters containing ferric oxyhydroxide media for wastewater P removal in a laboratory column test and in a full-scale domestic septic system. In the column test, during 30 mo of dosing with domestic wastewater, reductive iron dissolution reactions delivered consistent moderate concentrations of Fe into solution (2.9 ± 1.6 mg L), and influent PO-P of 3.7 ± 1.0 mg L was attenuated to 0.09 + 0.04 mg L in the column effluent (98% removal). Phosphorus breakthrough at successive locations along the column indicated that in addition to sorption, mineral precipitation reactions probably also played an important role in the observed P attenuation. This was supported by electron microprobe analyses, which showed the presence of thick (20 μm) secondary Fe-rich coatings containing P on the primary ferric media grains. Assays of NaHCO-leachable and acid-extractable P on the column solids showed accumulation of up to 5.4 mg g acid-extractable P near the column inlet, but <5% of this amount was easily desorbable, further indicating P attenuation from processes other than sorption. Over 19 mo of operation, the domestic septic system also showed generally consistent increased Fe in the filter effluent (2.6 ± 1.7 mg L) and achieved 99% P removal to 0.03 ± 0.02 mg L when the effluent was subsequently oxidized in a sand filter. Ferric iron filters could be attractive options for P removal in smaller wastewater systems because of their passive nature.     

Bioproduction of ferric sulfate used during heavy metals removal from sewage sludge

Toxic metals removal from wastewater sewage sludge can be achieved through microbial processes involving Acidithiobacillus ferrooxidans. The oxidation of ferrous ions by A. ferrooxidans, cultured in sewage sludge filtrate, was studied in both batch and continuous flow stirred tank reactors. Sewage sludge filtrate containing natural nutrients (phosphorus and nitrogen) was recovered as effluent following the dehydration of a primary and secondary sludge mixture. Batch and continuous flow stirred tank reactor tests demonstrated that A. ferrooxidans were able to grow and completely oxidize ferrous iron in a culture medium containing more than 80% (v v(-1)) sewage sludge filtrate with 10 g Fe(II) L(-1) added. Toxic levels were reached when total organic carbon in the sewage sludge filtrate exceeded 250 mg L(-1). The ferric iron solution produced in the sludge filtrate by A. ferrooxidans was used to solubilize heavy metals in primary and secondary sludge. The solubilization of Cu, Cr, and Zn yielded 71, 49, and 80%, respectively. This is comparable with the yield percentages obtained using a FeCl(3) solution. The cost of treating wastewater sewage sludge by bioproducing a ferric ion solution from sewage sludge is three times less expensive than the conventional method requiring a commercial ferric chloride solution.     

Rapid manganese removal from mine waters using an aerated packed-bed bioreactor

In the UK, the Environmental Quality Standard for manganese has recently been lowered to 30 microg/L (annual average), which is less than the UK Drinking Water Inspectorate's Maximum Permitted Concentration Value (50 microg/L). Current passive treatment systems for manganese removal operate as open-air gravel-bed filters, designed to maximize either influent light and/or dissolved oxygen. This requires large areas of land. A novel enhanced bioremediation treatment system for manganese removal has been developed that consists of a passively aerated subsurface gravel bed. The provision of air at depth and the use of catalytic substrates help overcome the slow kinetics usually associated with manganese oxidation. With a residence time of only 8 h and an influent manganese concentration of approximately 20 mg/L, >95% of the manganese was removed. The treatment system also operates successfully at temperatures as low as 4 degrees C and in total darkness. These observations have positive implications for manganese treatment using this technique in both colder climates and where large areas of land are unavailable. Furthermore, as the operation of this passive treatment system continually generates fresh manganese oxyhydroxide, which is a powerful sorbent for most pollutant metals, it potentially has major ancillary benefits as a removal process for other metals, such as zinc.     

MANGANESE OXIDATION RELATED TO THE RELEASES FROM RESERVOIRS1

ABSTRACT: Stratified reservoir waters frequently contain objectionable quantities of dissolved manganese. The oxidation and removal of dissolved manganese during transport below Normandy Dam, Tennessee, was shown to be much more rapid than expected from chemical oxidation. Oxidation took place in only a day of travel time rather than months or years. Laboratory studies showed that removal was associated with a slime found on rock surfaces below the dam and led to the development of column technology as a possible method of treating natural waters containing manganese. Hydraulic loadings on the columns in the range of 390–780 m³/hr.ha accomplished a 90 percent removal rate of soluble manganese over an influent concentration range of 2 to 15 mg/l.     

Phosphorus removal in vegetated filter strips

Vegetated filter strips (VFS) are used recently for removal, at or near the source, of sediment and sediment-bound chemicals from cropland runoff. Vegetation within the flowpath increases water infiltration and decreases water turbulence, thus enhancing pollutant removal by sedimentation within filter media and infiltration through the filter surface. Field experiments have been conducted to examine the efficiency of vegetated filter strips for phosphorus removal from cropland runoff with 20 filters with varying length (2 to 15 m), slope (2.3 and 5%), and vegetated cover, including bare-soil plots as control. Artificial runoff used in this study had an average phosphorus concentration of 2.37 mg L(-1) and a sediment concentration of 2700 mg L(-1). The average phosphorus trapping efficiency of all vegetated filters was 61% and ranged from 31% in a 2-m filter to 89% in a 15-m filter. Filter length has been found to be the predominant factor affecting P trapping in VFS. The rate of inflow, type of vegetation, and density of vegetation coverage had secondary influences on P removal. Short filters (2 and 5 m), which are somewhat effective in sediment removal, are much less effective in P removal. Increasing the filter length beyond 15 m is ineffective in enhancing sediment removal but is expected to further enhance P removal. Sediment deposition, infiltration, and plant adsorption are the primary mechanisms for phosphorus trapping in VFS.     

Iron and aluminium based adsorption strategies for removing arsenic from water

Arsenic is a commonly occurring toxic metal in natural systems and is the root cause of many diseases and disorders. Occurrence of arsenic contaminated water is reported from several countries all over the world. A great deal of research over recent decades has been motivated by the requirement to lower the concentration of arsenic in drinking water and the need to develop low cost techniques which can be widely applied for arsenic removal from contaminated water. This review briefly presents iron and aluminium based adsorbents for arsenic removal. Studies carried out on oxidation of arsenic(III) to arsenic(V) employing various oxidising agents to facilitate arsenic removal are briefly mentioned. Effects of competing ions, As:Fe ratios, arsenic(V) vs. arsenic(III) removal using ferrihydrite as the adsorbent have been discussed. Recent efforts made for investigating arsenic adsorption on iron hydroxides/oxyhydroxides/oxides such as granular ferric hydroxide, goethite, akaganeite, magnetite and haematite have been reviewed. The adsorption behaviours of activated alumina, gibbsite, bauxite, activated bauxite, layered double hydroxides are discussed. Point-of-use adsorptive remediation methods indicate that Sono Arsenic filter and Kanchan™ Arsenic filter are in operation at various locations of Bangladesh and Nepal. The relative merits and demerits of such filters have been discussed. Evaluation of kits used for at-site arsenic estimation by various researchers also forms a part of this review.     

A simulation experiment on the effectiveness of tree and pasture filter strips to remove NO3-N in lateral soil water flow

The impact of vegetative filter strips to reduce the delivery of nonpoint source pollutants from agricultural land to inland water systems is now recognized as an important element in overall agro-ecosystem management. A glasshouse experiment was undertaken to measure the effectiveness of tree (Eucalyptus camaldulensis Dehnh. and Casuarina cunninghamiana Mq.) and pasture filter strips to intercept lateral movement of NO(3)-N in soil water. Tree treatments retained significantly more NO(3)-N associated with shallow soil water movement (between the A and B soil horizons) than bare ground. Nitrate-N removal was not significantly different between trees and pasture, and among the tree treatments. However, uptake and accumulation of NO(3)-N by pastures was significantly (P < 0.001) greater than the trees. The average rates of N accumulation were 0.82 g m(-)(2) and 1.52 g m(-2) wk(-1) for the tree plots and the pasture plots, respectively. The experiment also showed that the efficiency of NO(3)-N removal from soil solutions by trees was greater when NO(3)-N concentrations were relatively higher in the soil (81.4% removal at 20 mg L(-1) compared to 68.1% at 10 mg L(-1)).     

纳米零价铁去除磷酸盐机理研究

纳米零价铁(nanoscale zero-valent iron,nZVI)颗粒具有独特核-壳结构,使其具有较强氧化还原特性,比表面积大和表面活性高等特点,因此被广泛用于不同环境介质中多种污染物的去除修复。本研究采用传统的液相化学还原法合成nZVI颗粒并用于去除水溶液中的磷酸盐。通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)和X射线衍射仪(XRD)表征nZVI颗粒的性质。实验研究了nZVI投加量、PO3-4初始浓度、溶液初始pH值对nZVI去除PO3-4效率的影响及微米零价铁(micro-ZVI)和nZVI去除PO3-4的对比。实验结果表明,当PO3-4初始浓度为20mg/L时,随着nZVI投加量从200mg/L增加到1000mg/L,PO3-4去除效率从32.94%上升到90.17%;当nZVI投加量为600mg/L时,随着PO3-4初始浓度从10mg/L增加到100mg/L,PO3-4去除效率从87.33%下降到45.77%;当nZVI投加量为600mg/L且PO3-4初始浓度为20mg/L,溶液pH分别为3和4时,PO3-4去除效率分别为83.63%和92.36%;nZVI和mZVI投加量均为600mg/L且PO3-4初始浓度为10mg/L,nZVI的PO3-4去除率(87.33%)是mZVI(8.86%)的9.86倍。研究结果表明,nZVI能够高效去除水体中的磷酸盐,主要去除机理是吸附和化学沉淀的双重作用。     

组合工艺处理上虞市总干渠微污染原水的中试启动研究

根据上虞市总干渠微污染原水水质特点,采用混凝沉淀＋曝气生物沸石滤池（ZBAF）＋活性炭滤池（GAC）组合工艺进行中试研究,考察了运行初期ZBAF的挂膜启动情况和组合工艺整体对此类水体的处理效果。结果表明：ZBAF在水温25℃~29℃、气水比1∶2、滤速2.5m/h下运行20天即挂膜成功;挂膜成熟后,组合工艺在5m/h滤速下对浊度、氨氮、UV254、CODMn的去除率分别达99%、85%、70%和75%,出水水质良好,浊度、氨氮、CODMn分别稳定在0.5NTU、0.1mg/L、1.5 mg/L以下。     

Interparticle diffusion and thermodynamic modeling studies for the removal of heavy metals using mixed adsorbents in industrial effluents

Pollution of water, air, and soil by industrial effluents is a major problem nowadays. A variety of contaminants are too responsible for changing the physicochemical properties of the receiving body. There are practical treatment solutions available to clean up contaminants from various resources. The term “adsorption” refers to one of them. The purpose of the research work is to remove heavy metals from industrial effluent. Mixed adsorbents prepared from activated charcoal and bone charcoals were used to remove the copper and cadmium ions. The experiment carried out in a batch operation and modeling of these data for intraparticle diffusion and thermodynamic calculations were reported in this research work. At optimum operating condition pH 6; metal ion concentration 50 mg/L; dose 5 g/L; agitation 180 rpm and temperature 40°C maximum 99.41% copper ions and 88.12% cadmium ion removal was achieved. Cadmium ions were well fitted in the thermodynamic model compared to copper ions, as demonstrated by the higher correlation coefficient R² (0.9824) value. Intra particle diffusion demonstrated that film diffusion was a rate-limiting step at the start of the reaction, while microporous intraparticle diffusion was the rate-determining phase later on. A Fourier transformation infrared spectroscopy, X-ray diffraction, and scanning electron micrography analysis confirmed the suitability of mixed adsorbents for the removal of cadmium and copper metal ions.