树脂纳米零价铁催化过硫酸钠降解甲基橙的研究

采用树脂负载零价纳米铁（NZVI-resin）作为铁源,活化过硫酸钠,产生硫酸根自由基氧化降解偶氮染料甲基橙。考察了温度、NZVI-resin加入量、pH值及过硫酸钠的浓度等因素对甲基橙降解率的影响,并对其降解动力学规律作了初步探讨。结果表明：降解反应遵循准一级反应动力学,在pH=3.0、Fe0=0.2 g.L-1、Na2S2O8=1.33 g.L-1的条件下,30 mg.L-1的甲基橙溶液降解率为99.7%。     

零价金属还原降解水中污染物的应用研究综述

介绍了零价金属在处理环境污染物中的具体应用,包括卤代有机物、重金属、硝基芳香族化合物、偶氮染料、高氯酸盐以及硝酸盐等,指出零价金属可以通过还原和混凝吸附等作用有效地治理环境污染物,并分析了零价金属处理污染物的特点和应用前景。     

固定化真菌漆酶对分散兰-2BLN的脱色和降解

采用改良壳聚糖固定化的真菌漆酶对染料分散兰-2BLN进行脱色和降解条件的研究,探索了固定化漆酶活力、处理时间、染料浓度、温度和pH对其降解效果的影响。结果表明,固定化漆酶脱色降解分散兰-2BLN的适宜条件为：固定化漆酶活力18.2U／mL,染料浓度100mg／L,温度40℃,pH4.6,在上述条件下降解1.5h,分散兰-2BLN脱色率能达到87.68％。重复分批使用固定化漆酶处理2BLN兰,在使用6批次后,脱色率仍能保持在55％以上,其催化效率得到了较大提高。     

偶氮染料的厌氧——好氧生物降解过程和影响因素

偶氮染料是总量最大、种类最多的合成染料,其降解处理通常采用厌氧-好氧技术。厌氧过程可实现偶氮染料的还原,好氧过程则完成还原产物芳香胺的去除。厌氧过程受偶氮染料结构和浓度、底物的种类和浓度、其他电子受体、氧化还原介体、温度和DO等环境因素以及水力停留时间的影响。好氧条件下芳香胺的降解过程受其自身的结构、浓度、外加碳源以及降解体系等影响,且自氧化过程影响了芳香胺的生物降解。在实际废水处理中应创造良好的条件提高偶氮染料的厌氧一好氧生物降解效率。     

零价铁还原脱氮技术研究进展

针对生物脱氮技术的缺点,对单纯零价铁及零价铁与生物耦合还原脱氮的效果、反应条件以及减少零价铁钝化现象的方法等进行了综述,以期为现有的污水处理厂升级改造提供理论依据和设计运行参数参考。同时为零价铁与生物耦合系统的研究方向提出了建议。     

磁性Ag_3PO_4/CuO/CuFe_2O_4纳米复合材料光催化降解亚甲基蓝

通过简易水热法结合沉积法制备了磁性Ag_3PO_4/CuO/CuFe_2O_4纳米复合材料。采用XRD、EDS、FESEM及UV-vis DRS对制备样品进行表征。对磁性纳米复合材料在可见光照射下降解染料亚甲基蓝(MB)的性能进行了研究。光照90 min后,磁性Ag_3PO_4/CuO/CuFe_2O_4纳米复合材料对MB的降解率高达89%,高于CuO/CuFe_2O_4及Ag_3PO_4对MB的去除。捕获实验证实在Ag_3PO_4/CuO/CuFe_2O_4光催化系统中超氧自由基和空穴是导致MB降解的主要活性物种。利用外加磁场可将催化剂回收再利用,经过三次循环降解后,磁性复合材料对MB的去除率仍可达到85%。     

纳米零价铁在应用中存在的问题及提高反应活性的方法

纳米零价铁对多种污染物质均有较好的去除效果,在污染的水体、土壤及底泥中被广泛研究与应用。前人对纳米零价铁的制备、在污染治理各方面的应用、作用的机理等方面进行了较为详细的总结,针对纳米零价铁在应用中存在的问题虽有提及,但少有人集中进行整理。本文主要针对纳米零价铁在环境治理方面存在的问题进行论述并对提高其反应活性的常用方法进行了总结,以期为纳米零价铁实际应用领域的深入研究提供借鉴并拓展新的思路。     

蒽醌染料活性艳蓝KN-R的化学氧化脱色和矿化

研究了使用NaClO化学氧化处理活性艳蓝KN-R模拟染料废水。分别以592nm、380nm、255nm波长处的吸光值为主要指标,跟踪染料的脱色降解。考察了NaClO投加量、染料浓度、温度和13H值等主要因素对模拟废水脱色的影响。结果表明：用NaClO化学氧化处理0．1mmolL^-1的活性艳蓝KN-R模拟染料废水,当NaClO与染料的摩尔比为18,T=30℃,13H值为7时,反应30分钟,脱色率可达到100％。pH值对脱色和TOC的去除有很大影响,酸性或中性条件下,染料快速脱色,30分钟后吸光值基本恒定,反应6个小时TOC的去除仍不明显;碱性条件下,染料缓慢脱色,但反应6个小时TOC的去除率可以达到40％左右。     

ClO_2对活性艳红K—2G和分散蓝2BLN染料的脱色研究

本论文主要利用自制高纯二氧化氯对两种常用且结构具有代表性的活性艳红K— 2G和分散蓝 2BLN料染 ,进行氧化脱色研究 ,作了温度 ,pH值 ,二氧化氯用量等条件试验 ,并用实际印染废水进行了实验 ,取得了良好的效果。在室温时 ,t =5min～ 7min ,pH值偏碱性条件下 ,单一染料溶液及混合染料溶液的脱色率均达到 90 %以上 ,实际印染废水的脱色也在 90 %左右。pH值、温度和ClO2 用量等多种因素对脱色率均有一定的影响 :pH值越高 ,染料脱色率越高。ClO2 用量存在一最佳值 ,与活性艳红K— 2G及分散蓝 2BLN染料的最佳摩尔比分别为 4 0及 2 0左右。ClO2 耗量随染料起始浓度的增大而增加 (脱色率相同时 )     

染料废水脱色的物理化学处理技术

染料废水目前主要的脱色方法有吸附、混凝、氧化还原和生化法.活性炭吸附适用于低浓度的染料废水处理.聚硅硫酸铁混凝效果与Fe/SiO4摩尔比和pH值相关.氢氧化镁可有效去除印染废水中的直接红染料.有机絮凝剂往往需要和其它药剂复配.氧化法脱色率大,但成本高昂,且受染料废水的组成、氧化性及pH值影响.还原法药剂价格低廉,但还原降解产物具有毒性,必须经过二次处理.生物法成本较低,又受制于染料的生物降解性.因此发展多种手段联合应用已是当前染料废水处理的研究方向.     

咪唑银配位聚合物吸附偶氮染料研究

以咪唑银配位聚合物{Ag（im）}n作吸附剂,对偶氮染料刚果红和甲基橙的吸附进行了研究,结果表明：刚果红的最佳吸附条件是吸附剂加入量为31．5mg,温度为30℃,pH值为3,吸附时间为70min,最高染料脱除率为90。7％;甲基橙的最佳吸附条件是吸附剂加入量为36．7mg,温度为30℃,pH值为2,吸附时间为50min,最高染料脱除率为58．3％。     

Fenton试剂高级氧化法降解甲基橙模拟废水研究

甲基橙是一种较难降解的有机苯环偶氮染料之一,研究其降解性能对其他染料废水体系的降解研究具有普遍参考价值。通过研究Fenton试剂降解甲基橙过程中的H202浓度、Fe2＋浓度、反应时间和反应体系pH值对甲基橙降解的影响,确定其最佳降解工艺条件为：当甲基橙浓度为20mg／L、pH值为3、Fe2＋浓度为1．5mmol／L、H2O2为32mmol/L时,降解率达到最大值（98．95％）。     

Ligand-assisted degradation of carbon tetrachloride by microscale zero-valent iron

Degradation of carbon tetrachloride (CT) by microscale zero-valent iron (ZVI) was investigated in batch systems with or without organic ligands (ethylenediaminetetraacetic acid (EDTA), citric acid, tartaric acid, malic acid and oxalic acid) at pHs from 3.5 to 7.5. The results demonstrated that at 25°C, the dechlorination of CT by microscale ZVI is slow in the absence of organic ligands, with a pseudo-first-order rate constant of 0.0217 h(-1) at pH 3.5 and being further dropped to 0.0052 h(-1) at pH 7.5. However, addition of organic ligands significantly enhanced the rates and the extents of CT removal, as indicated by the rate constant increases of 39, 31, 32, 28 and 18 times in the presence of EDTA, citric acid, tartaric acid, malic acid and oxalic acid, respectively, at pH 3.5 and 25°C. The effect of EDTA was most significant; the dechlorination of CT at an initial concentration of 20 mg l(-1) increased from 16.3% (no ligands) to 89.1% (with EDTA) at the end of 8h reaction. The enhanced CT degradation in the presence of organic ligands was primarily attributed to the elimination of a surface passivation layer of Fe(III) (hydr)oxides on the microscale ZVI through chelating of organic ligands with Fe(III), which maintained the exposure of active sites on ZVI surface to CT.     

Decolorization and Complete Degradation of Methyl Red by a Mixed Culture

Synthetic dyes, azo dyes in particular, are widely found in the effluents from textile industries. The persistence and toxicity of these compounds cause adverse impacts in the receiving streams. A mixed culture isolated from a domestic wastewater treatment plant was found to remove the colour of the azo dye, methyl red, efficiently. Total decolorization and degradation occurred within 18 h. The mixed culture could degrade 700 mgl^–1 of methyl red efficiently in the presence of 200 mgl^–1 of glucose, whereas in the absence of glucose it could degrade only 100 mgl^–1 of methyl red. The mixed culture, when suspended in phosphate buffer along with methyl red at 100 mgl^–1 concentration could degrade methyl red efficiently within 2 h of incubation. The pH of the medium decreased continuously during degradation. After the complete removal of initial methyl red, another 100 mgl^–1 was added to the culture filtrate and incubated further. The mixed microbial cultures could degrade methyl red efficiently through three cycles but further degradation was not possible as the pH of the medium decreased to 3.5.     

零价铁活化过硫酸盐降解污水中萘普生的研究

为了提高零价铁(ZVI)活化过硫酸盐(PS)的ZVI/PS体系对有机污染物萘普生(NAP)处理的技术水平,即实现对污水中NAP的有效降解.采用对比试验,通过设置不同投加量的PS与ZVI的方式,观察在不同酸碱度条件下NAP的降解量.研究结果表明,酸性条件下,当PS投加量为0.5mM或ZVI投加量为1.50mM时,NAP的...     

拟除虫菊酯农药的微波辅助无极汞灯下的降解机理研究

在水溶液中,以微波辅助无极汞灯(Microwave-Assisted Eletrodeless Discharge Mercury Lamp,MW-EDML)降解氯氰菊酯、甲氰菊酯和功夫菊酯等3种拟除虫菊酯农药(Synthetic pyrethroids,SPs),采用固相萃取(Solid Phase Extraction,SPE)富集后,用GC-MS鉴定降解产物,并根据降解产物重点探讨了SPs的降解机理。3种SPs的主要降解产物有6种,其降解途径有:酯键水解、氰基水解、脱羧、醚键断裂、氧化、苯环的羟基化以及与溶剂反应等。实验结果还表明:MW-EDML是个高效、简便的降解SPs类农药手段,可应用于其他有机污染物的降解过程。     

生物流化床处理生活污水的动力学研究

本研究采用颗粒活性炭（Granule Activated Carbon,GAC）为填料,考察了生物流化床（Biological fluidized Bed,BFB）处理生活污水的动力学.研究结果表明,GAC-BFB内生物膜的表现产率YoA为2.3057gVSS/gCOD,微生物细胞衰减常数Kd为0.3056d-1;基质降解动力学中米氏常数Ks为0.2182mg/L,反应速率常数K为13.09 mg/（l·h）.GAC-BFB的微生物生长动力学拟合方程为1/θc=2.3057q-0.3056,R2=0.9549; GAC-BFB的基质降解动力学拟合方程为1/U =0.2182＊1/S ＋0.0764,R2 =0.9972,该微生物生长动力学拟合方程及基质降解动力学拟合方程能较好的反映GAC-BFB系统的出水水质状况,本研究所获得的动力学关系和动力学参数可作为GAC-BFB系统的设计依据.     

Microbial remediation of nitro-aromatic compounds: an overview

Nitro-aromatic compounds are produced by incomplete combustion of fossil fuel or nitration reactions and are used as chemical feedstock for synthesis of explosives, pesticides, herbicides, dyes, pharmaceuticals, etc. The indiscriminate use of nitro-aromatics in the past due to wide applications has resulted in inexorable environmental pollution. Hence, nitro-aromatics are recognized as recalcitrant and given Hazardous Rating-3. Although several conventional pump and treat clean up methods are currently in use for the removal of nitro-aromatics, none has proved to be sustainable. Recently, remediation by biological systems has attracted worldwide attention to decontaminate nitro-aromatics polluted sources. The incredible versatility inherited in microbes has rendered these compounds as a part of the biogeochemical cycle. Several microbes catalyze mineralization and/or non-specific transformation of nitro-aromatics either by aerobic or anaerobic processes. Aerobic degradation of nitro-aromatics applies mainly to mono-, dinitro-derivatives and to some extent to poly-nitro-aromatics through oxygenation by: (i) monooxygenase, (ii) dioxygenase catalyzed reactions, (iii) Meisenheimer complex formation, and (iv) partial reduction of aromatic ring. Under anaerobic conditions, nitro-aromatics are reduced to amino-aromatics to facilitate complete mineralization. The nitro-aromatic explosives from contaminated sediments are effectively degraded at field scale using in situ bioremediation strategies, while ex situ techniques using whole cell/enzyme(s) immobilized on a suitable matrix/support are gaining acceptance for decontamination of nitrophenolic pesticides from soils at high chemical loading rates. Presently, the qualitative and quantitative performance of biological approaches of remediation is undergoing improvement due to: (i) knowledge of catabolic pathways of degradation, (ii) optimization of various parameters for accelerated degradation, and (iii) design of microbe(s) through molecular biology tools, capable of detoxifying nitro-aromatic pollutants. Among them, degradative plasmids have provided a major handle in construction of recombinant strains. Although recombinants designed for high performance seem to provide a ray of hope, their true assessment under field conditions is required to address ecological considerations for sustainable bioremediation.