接触絮凝研究进展

接触絮凝的概念源于直接过滤 ,是指介质存在时的絮凝作用。由于简便易行、处理效果良好 ,接触絮凝方法处于迅速发展之中 ,并且具有广泛的应用前景。其研究范围包括物理、化学、胶体界面过程等相互作用。本文以溶液中的颗粒物相互作用为基础 ,对接触絮凝理论的发展加以简要概述     

某生活垃圾卫生填埋场渗滤液的梯度分离与表征

目前,渗滤液中污染物的粒度分布及其在渗滤液污染控制中的作用日益受到关注。通过系列微滤膜(1.2μm及0.45μm)对某生活垃圾卫生填埋场渗滤液各处理单元的渗滤液进行梯度分离,发现悬浮物对COD、浊度的影响较大;COD主要在胶体态和可溶解态间分配,不同渗滤液中的分配情况不同;磷主要与胶体、悬浮物以各种形式结合而存在;细胶粒和溶解态等小分子对TN的贡献大;不同粒度物质对pH的影响不明显;总残渣在可溶态组分中所占比例较大。膜微滤处理渗滤液可以有效的去除一部分物质,使COD、TP、TN、浊度、电导率都有不同程度的降低,pH逐渐升高,但对总N、残渣的去除效果不好。     

接触氧化-人工湿地去除印染废水中的COD

采用絮凝沉淀+接触氧化+人工湿地工艺处理印染废水中COD研究。结果表明,斜板沉淀池出水COD平均值为1322mg/L,此间COD去除率为38·6%;二沉池出水COD平均值为71mg/L,此段COD去除率达94·6%;人工湿地出水COD平均值为37mg/L,人工湿地COD去除率为48·0%。处理设施COD总去除率98·3%。     

Effect of operational parameters on the removal of particulate chemical oxygen demand in the activated sludge process.

The removal of particulate material in the aeration basin of the activated sludge process is mainly attributed to bioflocculation and hydrolysis of particulate substrate. The bioflocculation process in the aeration tank of the activated sludge process occurs only under favorable conditions in the system, and several common operational parameters affect its performance. The principal objective of this research was to observe the effect of mixed liquor suspended solids, solids retention time (SRT), and extracellular polymer substances on the removal of particulate substrate by bioflocculation. A first-order particulate removal expression, based on flocculation, accurately described the removal rates for supernatant suspended solids and colloidal chemical oxygen demand. Based on the results presented in this investigation, a mixed liquor concentration of approximately 2200 mg/L, an SRT of at least 3 days, and a contact time of 30 minutes are needed for relatively complete removal of the particulate substrate in a plug-flow reactor.     

不同来源高浓度有机废水的集中处理

按照水质情况,将多种来源于不同工业生产过程中的高浓度有机废水划分为高悬浮固体乳化液废水、难生化高浓度有机废水、高悬浮固体不含油有机废水、含铬有机废水和杂质含量较少的乳化液废水5类,分别采用酸化破乳/Fen-ton氧化/混凝/絮凝、Fenton氧化/混凝/絮凝、混凝/絮凝、还原/混凝/絮凝、震动膜过滤技术作为生化预处理技术,并通过小试和中试验证了各技术的效果。实验结果表明,按照上述分类结果,采用不同预处理技术可以得到良好的效果,废水水质明显改善,满足继续生化处理的基本条件。各预处理生产装置处理效果稳定,同时生化系统已经稳定运行120天以上,COD去除率超过90%,出水经过低剂量的Fenton试剂处理后可达到《污水排入城镇下水道水质标准》(CJ343-2012)。     

微波辅助工艺处理天然气净化废水的应用研究

进行了微波辅助工艺处理天然气净化废水的应用研究,考察了废水色度、COD、SS、含油量和细菌的去除效果以及对废水腐蚀率的降低作用,并进行了同等条件下的常温对照实验。研究结果表明:微波絮凝工艺中絮凝剂PAC和PAM的用量较常温下减少了100 mg/L和5 mg/L,絮凝沉降时间仅为常温絮凝的1/4,最佳微波辐照时间下废水的COD去除率比常温条件下提高4.6%。微波工艺处理后,难降解天然气净化废水的含油量去除率达到了94%、废水中硫酸盐还原菌死亡率达97%以上,废水腐蚀率降为原来的1/7,废水可生化性得到了很大提高,可直接进行好氧生化处理。实验表明,微波辅助工艺对难降解天然气净化废水具有很好的处理应用效果。     

光助Fenton氧化、化学絮凝法联合处理R盐废水的研究

采用光助Fenton氧化、化学絮凝法联合处理生物难降解的R盐废水,考察了不同反应条件对处理效果的影响。试验结果表明,光助Fenton氧化、化学絮凝法联合处理废水,两者之间存在协同作用,可以提高处理效果,降低处理成本。在最佳试验条件下,R盐废水经光助Fenton氧化、化学絮凝法联合处理后,COD去除率可达90%以上。     

光助Fenton氧化、化学絮凝法联合处理R盐废水的研究

采用光助Fenton氧化、化学絮凝法联合处理生物难降解的R盐废水,考察了不同反应条件对处理效果的影响.试验结果表明,光助Fenton氧化、化学絮凝法联合处理废水,两者之间存在协同作用,可以提高处理效果,降低处理成本.在最佳试验条件下,R盐废水经光助Fenton氧化、化学絮凝法联合处理后,COD去除率可达90%以上.     

实用型深度光氧化设备对几种染料和多菌灵农药废水的处理

利用HFS 1型深度光氧化废水处理设备对活性艳蓝K3R、酸性红 3B、活性黑KNB、酸性红A、直接耐酸大红4BS等 5种染料的水溶液和多菌灵农药废水进行了深度光氧化处理。结果表明 :(1)染料在处理 5min后 ,脱色率都在 90 %以上 ;处理 15min后 ,CODCr的去除率除活性艳蓝K3R较低外 ,其余的都在 80 %以上 ;BOD5/CODCr的值都有所增大。 (2 )多菌灵农药废水 (经稀释 )处理 4 0min后CODCr的去除率为 5 7.0 % ,BOD5/CODCr的值由 0 .2 0增加到 0 .4 4。 (3)采用深度光氧化 -絮凝的工艺处理多菌灵农药废水 ,CODCr的去除率为 5 7.5 %。     

Appropriate combination of physico-chemical methods (coagulation/flocculation and ozonation) for the efficient treatment of landfill leachates

An integrated technique consisted of ozonation and coagulation/flocculation processes was studied, aiming to provide an efficient method for the treatment of stabilized/biologically pre-treated leachates, in order to reduce the organic pollutants' content to concentration values lower than the corresponding limits, imposed by the legislation. Leachates were collected from a municipal landfill site; samples containing around 1000 mg l(-1) COD and BOD(5)/COD ratio about 0.17 were treated by using two different processes or combinations between them, i.e. ozonation, coagulation-flocculation, ozonation followed by coagulation/flocculation and coagulation/flocculation followed by ozonation. The application of single ozonation resulted to the efficient removal of color and organic loading, due to the respective oxidation, induced by ozonation; however, COD values lower than 200 mg l(-1) could be only achieved after prolonged reaction times and for high ozone production rates. The coagulation of leachate samples was studied by the addition of ferric chloride or poly-aluminum chloride agents at various dosages. Maximum COD removal rates (up to 72%) were achieved by the addition of 7 mM Fe, or of 11 mM Al respectively. However, final COD values higher than 200 mg l(-1) were obtained indicating the requirement of an additional treatment step. Pre-ozonation followed by coagulation/flocculation was not found to be an efficient treatment approach for this aim, but coagulation/flocculation followed by ozonation, was proved to be an efficient process for the reduction of COD to lower than 180 mg l(-1).     

Influence of organic matter on arsenic removal by continuous flow electrocoagulation treatment of weakly mineralized waters

The aim of this study is to evaluate and understand the electrocoagulation/flocculation (ECF) process to remove arsenic from both model and natural waters with low mineral content and to compare its performances to the coagulation/flocculation (CF) process already optimized. Experiments were thus conducted with iron electrodes in the same specific treatment conditions (4≤current density (mAcm(-2))≤33) to study the influence of organic matter on arsenic removal in conditions avoiding the oxidation step usually required to improve As(III) removal. The process performance was evaluated by combining quantification of arsenic residual concentrations and speciation and dissolved organic carbon residual concentrations with zeta potential and turbidity measurements. When compared to CF, ECF presented several disadvantages: (i) lower As(V) removal yield because of the ferrous iron dissolved from the anode and the subsequent negative zeta potential of the colloidal suspension, (ii) higher residual DOC concentrations because of the fractionation of high molecular weight compounds during the treatment leading to compounds less prone to coagulate and (iii) higher residual turbidities because of the charge neutralization mechanisms involved. However, during this process, As(III) was oxidized to As(V) improving considerably its removal whatever the matrix conditions. ECF thus allowed to improve As(III) removal without applying an oxidation step that could potentially lead to the formation of toxic oxidation by-products.     

加药量和水力搅拌速度对雨水混凝效果的影响

为降低分流制雨水中悬浮颗粒物及其他污染物浓度,减轻城市景观河道的水体富营养化程度,对取自泵站的雨水进行混凝沉淀工艺优化实验。以PAC为混凝剂,采用Zeta电位仪、激光粒度仪和iPDA在线监测技术对混凝过程进行监测,考察了混凝剂投加量和水力搅拌速度对絮体形成和分流制雨水处理效果的影响,结果表明,混凝剂投加量和混合水力搅拌速度直接影响絮体Zeta电位和聚沉特性;混合搅拌速度控制混凝反应速率,絮凝速度梯度影响絮体形成粒径。FI曲线特征参数对控制混凝工艺具有指导意义。PAC投加量为35 mg/L,混合阶段搅拌速度800 r/min,搅拌30 s,絮凝阶段采用150、108和60 r/min的转速各自搅拌5 min,沉后水中剩余颗粒总数最少,浊度、COD和总磷去除效果最佳。     

Improvement of upflow anaerobic sludge bed performance using chitosan.

Chitosan, with a degree of deacetylation of 85% and a molecular weight of 2.5 x 10(5) Da, yielding high flocculation efficiency (85 to 100% flocculation) and a broad flocculation region (2 to 45 mg/g suspended solids), was selected for accelerating granulation in a 30-L upflow anaerobic sludge bed (UASB) used to treat wastewater from a tropical fruit-processing industry. Compared with other studies, smaller amounts of chitosan were applied (two injections with 2 mg chitosan/g suspended solids in the reactor at each injection). Comparison with the UASB without chitosan addition, the UASB had a 24 to 37% larger particle size and a 6 to 41% longer solids retention time. In addition, the reactor performances were also enhanced. The UASB with chitosan addition had a 9 to 59% lower effluent chemical oxygen demand (COD), 4 to 10% higher COD removal, up to 35% higher biogas production rate, and a 16 to 68% lower biomass washout. The paired t-test analysis indicated that these performance parameters were significantly different (P < 0.05).     

脱木素工艺处理造纸废水的实践与机理

脱木素工艺为中小制浆企业的黑液治理提供了新的方法。系统中酸化纤维污泥减小碱木素胶粒间的斥力 ,吸附废水中已析出的木质素和细小纤维 ;酸破坏了系统中胶体的水化膜 ,增大了胶体的粒径 ;混凝剂中和胶体表面电荷 ,增加颗粒间的接触机会 ,同时发挥了絮凝沉降的作用。该工艺与传统工艺相比 ,减少了酸及混凝剂的用量 ,木素沉降速度快。当试验废水pH =5、绝干纤维污泥与进水CODCr质量之比为 1.1、硫酸铝投加量为 160mg/L时 ,CODCr去除率高于 63 %。     

Pre-oxidation and coagulation of textile wastewater by the Fenton process

This paper evaluates the Fenton process, involving oxidation and coagulation, for the removal of color and chemical oxygen demand (COD) from synthetic textile wastewater containing polyvinyl alcohol and a reactive dyestuff, R94H. The experimental variables studied include dosages of iron salts and hydrogen peroxide, oxidation time, mixing speed and organic content. The results show that color was removed mainly by Fenton oxidation. The color removal reached a maximum of 90% at a reaction time of 5 min under low dosages of H2O2 and Fe2+. In contrast, the COD was removed primarily by Fenton coagulation, rather than by Fenton oxidation. The ratio of removal efficiency between Fenton process and ferric coagulation was 5.6 for color removal and 1.2 for COD removal. It is concluded that Fenton process for the treatment of textile wastewater favors the removal of color rather than COD.     

水解酸化-接触氧化-混凝气浮工艺处理高浓度漂染废水

本文介绍了水解酸化 -接触氧化 -混凝气浮工艺在处理高浓度漂染废水中的工程应用。结果表明 ,漂染废水经该工艺处理后CODCr去除率为 95 % ,色度去除率为 90 %。该工艺具有占地面积小 ,脱色效果好 ,处理效率高等特点 ,能广泛应用于纺织漂染废水的实际工程中     

Fe (III) supported on resin as effective catalyst for the heterogeneous oxidation of phenol in aqueous solution

FeIII supported on resin as an effective catalyst for oxidation was prepared and applied for the degradation of aqueous phenol. Phenol was selected as a model pollutant and the catalytic oxidation was carried out in a batch reactor using hydrogen peroxide as the oxidant. The influent factors on oxidation, such as catalyst dosage, H2O2 concentration, pH, and phenol concentration were examined by considering both phenol conversion and chemical oxygen demand (COD) removal. The FeIII-resin catalyst possesses a high oxidation activity for phenol degradation in aqueous solution. The experimental results of this study show that almost 100% phenol conversion and over 80% COD removal can be achieved with the FeIII-resin catalyst catalytic oxidation system. A series of prepared resin were investigated for improving the oxidation efficiency. It was found that the reaction temperature and initial pH in solution significantly affected both of phenol conversion and COD removal efficiency. The activity of the catalyst significantly decreased at high pH, which was similar to the Fenton-like reaction mechanism. Results in this study indicate that the FeIII-resin catalytic oxidation process is an efficient method for the treatment of phenolic wastewater.     

Advanced oxidation treatment of physico-chemically pre-treated olive mill industry effluent

In this study, the applicability of physico-chemical methods was investigated for the pre-treatment of the olive mill effluents prior to the discharge into the common sewerage ending with a municipal wastewater treatment plant. The samples were taken from an olive oil industry operated as three-phase process located in Turkey. Various pre-treatment methods including acid craking, polyelectrolyte and lime additions were applied. Advanced oxidation study using Fenton's process was also investigated following pre-treatment by acid cracking and cationic polyelectrolyte. Acid cracking alone gave satisfactory treatment efficiencies and polyelectrolite additions to the acid-cracked samples enhanced treatment efficiency. Since a complete treatment plant is available at the end of the sewer system, results indicated that the effluents of the investigated industry could be discharged into the municipal sewerage in the case of total chemical oxygen demand (COD(tot)), suspended solid (SS) and volatile suspended solid (VSS) concentrations according to the Turkish Water Pollution Control Regulation after pre-treatment with 5 ppm anionic polyelectrolyte following acid cracking. The minimum COD(tot), SS and VSS removals were observed when raw wastewater was pre-treated with lime and the discharge standards to the municipal sewer system could not be met. Advanced oxidation with Fenton's process was applied after acid cracking and cationic polyelectrolyte treatment in order to investigate further reduction in chemical oxygen demand (COD) concentration for minimizing the influence of this industrial discharge on the existing municipal wastewater treatment plant. Results indicated that COD(tot) removal increased up to 89% from 74% after Fenton's oxidation for the acid cracked samples in which cationic polyelectrolite (10 ppm) was added.     

Transformation characteristics of refractory pollutants in plugboard wastewater by an optimal electrocoagulation and electro-Fenton process

The treatment of the plugboard wastewater was performed by an optimal electrocoagulation and electro-Fenton. The organic components with suspended fractions accounting for 30% COD were preferably removed via electrocoagulation at initial 5 min. In contrast, the removal efficiency was increased to 76% with the addition of H(2)O(2). The electrogenerated Fe(2+) reacts with H(2)O(2) and leads to the generation of (·)OH, which is responsible for the higher COD removal. However, overdosage H(2)O(2) will consume (·)OH generated in the electro-Fenton process and lead to the low COD removal. The COD removal efficiency decreased with the increased pH. The concentration of Fe(2+) ions was dependent on the solution pH, H(2)O(2) dosage and current density. The changes of organic characteristics in coagulation and oxidation process were differenced and evaluated using gel permeation chromatography, fluorescence excitation-emission scans and Fourier transform infrared spectroscopy. The fraction of the wastewater with aromatic structure and large molecular weight was decomposed into aliphatic structure and small molecular weight fraction in the electro-Fenton process.     

UASB+AF-生物接触氧化工艺处理皂素-酒精综合废水

采用水解酸化-UASB+AF-接触氧化工艺处理黄姜皂素-酒精综合废水,经调试启动和运行研究,结果表明:当进水COD在10 000~12 800 mg/L时,最终出水COD浓度可降低到200 mg/L以下;水解酸化、UASB+AF和接触氧化各阶段的COD去除率分别达到23%、75%和93.5%,系统总的COD去除率可达到98.4%,出水色度在30~50倍之间;同时该工艺具有运行稳定、耐冲击负荷能力强等特点。