Anaerobic decolorization of an azo dye by a mixed culture

Wool dyeing wastewater contains xenobiotic compounds that can be removed by biotechnological processes. Studies on various dyes showed that anaerobic processes are suitable to alter azo dyes as a first step of the biodegradation process. These compounds are reduced by anaerobic consortia to aromatic amines and its ultimate degradation can be achieved by a further aerobic treatment.

Studies on degradation rate of an wool acid dye were performed in batch systems inoculated with anaerobic biomass. A commercial diazo dye, Acid Red 73, was added to the synthetic medium in which glucose was used as sole carbon source.

Results indicated that the Acid Red 73 was partially degraded by a mixed culture of anaerobic bacteria and a decolorization of 90% was obtained. Kinetics studies on removal of the colour showed that the decolorization rate was several times faster than the degradation rate of glucose for a range of dye concentrations between 60 mg/L and 400 mg/L. A first order kinetic model was used for dye concentrations up to 200 mg/L. For higher concentrations a model similar to the Michaelis‐Menten equation was better fitted to the experimental data.     

吸附菌HX5对活性艳蓝KN-R的吸附脱色作用

研究了吸附菌HX5对活性艳蓝KNR的吸附脱色作用,碳源、氮源、盐度和染料浓度对KNR吸附脱色的影响,以及HX5生长菌体对KNR的脱色机理.结果表明,菌株HX5对KNR脱色的最佳碳、氮源分别为葡萄糖和硫酸铵;碳源浓度在10g/L以上时,可使200mg/L的KNR完全脱色,碳源浓度过高,脱色效果不显著;HX5对KNR脱色的最佳氮源浓度为0.75g/L,在0～2%的浓度范围内,盐度对脱色无显著影响;染料对菌株HX5具有一定的生长抑制毒性,但对于400mg/L的KNR,脱色率仍可达95.1%;HX5生长菌体对KNR作用96h内主要为生物吸附作用,96h外则可能发生了生物降解.图5表2参9     

酸性染料的臭氧降解与中间产物

以酸性金黄G模拟染料废水为研究对象,观察臭氧氧化过程中染料溶液吸光度和TOC的变化,利用离子色谱仪、红外光谱仪和GC/MS对染料的降解过程进行了分析,并用发光细菌法检测了溶液急性毒性的变化,结果表明,臭氧对染料的降解符合一级反应动力学,反应40 min后染料溶液的脱色率达到99.3%,TOC去除率为35.7%;染料分子中的S有97.8%被转化为SO2-4,分子中的仲胺基部分转化成酰胺基,水解后生成NH+4,最终氧化成NO-3,溶液中有草酸产生;溶液在臭氧化前期由于生成了醛类和酚类物质,使急性毒性首先呈上升趋势,25min后随着氧化的深入,溶液毒性开始逐渐下降,     

耐高盐撕裂蜡孔菌P2对模拟橙黄G染料废水的脱色及废水脱色前后的毒性测试

为评价撕裂蜡孔菌P2处理橙黄G染料废水的应用潜力,采用批次实验在开敞系统中研究静置与摇动、染料初始浓度、pH、温度、盐度、碳源、氮源、金属离子等因子对该菌降解橙黄G染料废水的影响,同时利用植物萌发与微生物抑菌试验进行染料与脱色溶液的毒性测试.结果表明,与摇动培养相比,静置培养更适合于撕裂蜡孔菌的脱色,最适脱色pH与温度分别为9和25℃.盐度测试结果显示撕裂蜡孔菌能在浓度为128 g L-1的盐溶液中能进行高效脱色,可达70%以上.在上述参数体系的优化基础上,分别进行了碳源、氮源与金属离子的添加优化实验,结果显示碳源、氮源与金属离子的最适浓度分别为4 g L-1葡萄糖、0.15 g L-1硝酸铵和0.1 mmol L-1 Zn2+.菌丝吸附在整个脱色过程中作用较小,撕裂蜡孔菌对橙黄G的脱色过程以酶的降解为主,未发现该菌分泌漆酶,只分泌锰过氧化物酶与木质素过氧化物酶,其最高活性分别为230 U mL-1和158 U mL-1.植物与微生物毒性分析显示撕裂蜡孔菌脱色后的产物对植物与微生物的毒性大大降低.因此,撕裂蜡孔菌对于处理橙黄G染料废水具有良好的应用潜力.     

Biological Decolorization of C.I. Basic Green 4 Solution by Chlorella sp.： Effect of Operational Parameters

In recent years, the ability of microorganisms to decolorize textile wastewater has received great attention due to the environmental persistence and toxicity of these pollutants. In this paper biological decolorization of triphenylmethane dye, C.I. Basic Green 4 (BG 4), by Chlorella species was investigated. The effect of operational parameters (temperature, pH, initial dye concentration and algal concentration) on decolorization efficiency was examined. Results indicated that the desired initial pH was 9. The stability and efficiency of the algae in long-term repetitive operations were also examined. Michaelis-Menten kinetics was employed to describe the apparent correlation between the decolorization rate and dye concentration. The optimal kinetic parameters, Vmax (specific decolorization rate) and Km (maximum specific decolorization rate) were 4.6 mg dye g cell-1 h-1and 151.0 mg L-1, respectively. Fig 10, Tab 2, Ref24     

一株能产生聚乙烯醇降解酶的委内瑞拉链霉菌

以聚乙烯醇(PVA)为唯一碳源,从土壤中筛选到1株能产生胞外PVA降解酶的放线菌GY1.根据扩增出的该菌株的16SrDNA全序列在GenBank中的比较结果,结合生理生化实验、细胞化学成分及菌落形态分析,确定该菌为委内瑞拉链霉菌(Stretopmycesvenezuelae).GY1菌株以PVA为唯一碳源时,产生的PVA降解酶活性达到120UL-1,是以葡萄糖或可溶性淀粉为唯一碳源时的10倍.当在PVA培养基中添加1gL-1至3gL-1的葡萄糖时,该菌株细胞量和PVA降解酶总酶活随着葡萄糖添加量的增加而增加,最大细胞量是未添加葡萄糖时的2.4倍,最高总酶活是未添加葡萄糖时的2.6倍,而单位质量细胞产生PVA降解酶的能力提高不大.但当添加的葡萄糖浓度从3gL-1增至10gL-1时,总酶活随着细胞量的增加出现下降趋势,同时单位质量细胞产生PVA降解酶的能力也大大降低.在相同PVA聚合度下,高醇解度PVA比低醇解度PVA更有利于GY1菌株的生长及产生PVA降解酶.图5表1参16     

黄孢原毛平革菌对固体介质中染料的降解反应

用黄孢原毛平革菌(Phanerochaetechrysosporium)3品系在固体介质中建立染料的降解反应体系,分光光度法测定染料的脱色降解率。黄孢原毛平革菌在琼脂、沙子及土壤等固体介质中均能有效地降解偶氮染料、蒽醌染料及聚合染料;植物材料玉米芯和木屑可作为共代谢碳源被该菌利用;BKM F 1767菌种降解能力最强,对活性艳蓝KN R的进攻性优于对PolyR 478和比布列希猩红。     

阳离子表面活性剂十六烷基三甲基溴化铵（CTAB）对磷钨酸(PW12)光催化还原降解偶氮染料直接耐晒黑G的影响

以磷钨酸H3PW12O4（PW12）为光催化剂,异丙醇（IS）作为电子给体,研究阳离子表面活性剂十六烷基三甲基溴化铵（CTAB）对PW12光催化还原降解直接耐晒黑G（DB19）的影响.考察了CTAB浓度、pH值、DB19初始浓度等因素对反应的影响,并采用一级反应动力学对反应过程进行分析.结果表明CTAB增强了PW12对直接耐晒黑G的还原脱色作用,CTAB浓度增加,DB19的光催化脱色速率提高.PW12用量对DB19还原脱色的影响程度和趋势与溶液中CTAB浓度有关,当CTAB浓度为0.10 mmol.L-1时,DB19的脱色速率随PW12用量的增加而增加;CTAB浓度为0.05 mmol.L-1,PW12用量为200 mg.L-1时DB19的脱色速率最快,继续增加反而降低.DB19还原脱色速率随其初始浓度升高而降低.另外,通过循环伏安法和暗反应明确还原态杂多蓝对染料的还原脱色作用,并借助UV-Vis光谱研究DB19、PW12、CTAB之间的相互作用,探索CTAB对PW12/IS光催化还原降解DB19的作用机理.该研究结果表明阳离子表面活性剂CTAB能够增强偶氮染料废水的PW12催化还原脱色处理.     

Evaluation of kinetics and energy consumption of the electrochemical oxidation of Acid Red 73 in aqueous media

A laboratory scale, undivided electrolysis cell with platinum anode and cathode was used for electrochemical oxidation of the azo dye Acid Red 73 in simulated wastewater. The influence of the supporting electrolyte, applied voltage, pH, initial dye concentration and temperature was studied, and decolorization was monitored by UV/Vis spectroscopy. Energy consumption, current efficiency and the electric energy per order have been also determined. With NaCl (1.5 g L^?1) as supporting electrolyte, at a voltage of 6 V, at neutral pH (6.9) and at 25 °C, the solution of the dye (50 mg L^?1) was completely decolorized within 15 min. The apparent activation energy for electrochemical decolorization was determined as ?1.9 kJ mol^?1.     

过硫酸钠氧化脱色罗丹明B——影响因素和机理

采用过硫酸钠(PDS)直接氧化和催化活化氧化脱色罗丹明B(RhB),分别考察了PDS剂量、pH、催化剂、Cl-浓度对RhB脱色的影响.结果表明,PDS在无外加催化剂下能够有效脱色RhB,pH越低,脱色率越高;当pH 2.4,PDS用量为3.5 g·L^-1,在120 min内RhB的脱色率可达92%;自由基淬灭实验表明,酸性条件下主要为PDS直接氧化脱色RhB,并存在小部分硫酸根自由基(SO₄4·-)作用.在pH 5.6、pH 8.0条件下,外加活性炭纤维(ACF)、四氧化三铁(Fe₃O₄4)、Fe₃O₄4负载型催化剂(ACF/Fe3O₄4)可促进PDS对RhB脱色;在pH 2.4条件下,外加ACF对RhB脱色的促进作用较小,Fe₃O₄4、ACF/Fe₃O₄4对RhB脱色有一定抑制作用.不同pH和催化剂处理下,低浓度Cl-(0.01、0.04 mO₄l·L^-1)对RhB脱色速率都呈现抑制作用,高浓度Cl-(0.08 mO₄l·L^-1)相对于低浓度Cl-处理都呈促进作用.不同浓度Cl-处理在反应前60 min RhB脱色速率差异较大,而反应120 min后脱色率差异较小.提出Cl-通过调控SO₄4·-脱色RhB途径来影响RhB脱色速率的机理,Cl-竞争消耗SO₄4·-降低RhB脱色速率,但经一系列反应生成的Cl2·-能与RhB快速反应而提高RhB脱色速率;Cl-对RhB的脱色反应速率的影响存在抑制-促进双重机制,且与Cl-浓度相关.研究结果为基于PDS直接氧化和催化氧化处理含盐染料废水的研究和应用提供了一定的理论依据.     

Adsorptive removal of Drimarine Red HF-3D dye from aqueous solution using low-cost agricultural waste: batch and column study

This study involves the utilisation of peanut husk for the removal of Drimarine Red HF-3D dye from aqueous solutions. Batch study experiments were conducted with native, HNO₃-treated and Na-alginate-immobilised peanut husk biomass. Maximum dye removal (95.24 mg/g) was obtained with HNO₃-treated biomass. The experimental data were successfully explained with a pseudo-second-order kinetic model for all types of biosorbents. The equilibrium data fitted well to the Freundlich adsorption isotherm model. A thermodynamic study was also carried out to check the nature of the adsorption process. A fixed-bed column study for Drimarine Red HF-3D was carried out to optimise the effect of bed height, flow rate and initial dye concentration using peanut husk biomass. The column study showed that biosorption capacity increased with the increase in initial dye concentration and bed height, but decreased with increased flow rate. Data for Drimarine Red HF-3D were in very good agreement with the bed depth service time model. Fourier transform infrared analysis demonstrated the involvement of different functional groups in dye biosorption. These results showed that peanut husk biomass possessed good potential for the removal of Drimarine Red HF-3D from aqueous solution.     

壳聚糖/膨润土复合絮凝剂处理染料废水的研究

利用壳聚糖/钠基膨润土复合絮凝剂对活性艳红X3B等11种染料模拟废水及实际印染废水进行絮凝脱色处理。考察了复合絮凝剂投加量、pH值、搅拌速率、搅拌时间等因素对模拟染料废水絮凝脱色的影响。结果表明,在染料浓度为100 mg.L-1,pH为5的条件下,复合絮凝剂投加量为1.25 g.L-1时,3种质量比的复合絮凝剂对活性艳红X3B的脱色率分别达到75%、90%和97%以上;质量比为1∶10的壳聚糖/钠基膨润土复合絮凝剂,对其它活性、还原性、分散性、水溶性等8种印染厂常用染料也具有很好的絮凝脱色作用,脱色率均可达94%以上。对印染废水处理厂进水口废水和经过A/O处理后废水的色度去除率和COD去除率分别可以达到81.05%、83.74%和53.21%、41.22%,具有一定的应用前景。     

Decolorization of azo dyes by a salt-tolerant Staphylococcus cohnii strain isolated from textile wastewater

The salt-tolerant Staphylococcus cohnii strain, isolated from textile wastewater, has been found effective on decolorizing several kinds of azo dyes with different structures. The optimal conditions for azo dye acid red B (ARB) decolorization by S. cohnii were determined to be pH = 7.0 and 30°C. The decolorization efficiency increased with the increase of the salinity concentration, and around 90% of ARB (100 mg·L^?1) could be decolorized in 24 h when the salinity concentration was up to 50 g·L^?1. Moreover, the strain could still decolorize 19% of ARB in 24 h even when the NaCl concentration was increased to 150 g·L^?1. Meanwhile, the dependence of the specific decolorization rate by S. cohnii on the ARB concentration could be described with Michaelis-Menten kinetics (K _m = 585.7mg·L^?1, V _max = 109.8 mg·g cell^?1·h^?1). The addition of quinone redox mediator, named 2-hydroxy-1,4-naphthoquinone and anthraquinone-2,6-disulfonate, significantly accelerated the decolorization performance of S. cohnii. Furtherly, the activities of azoreductase (0.55 ??mol·mg protein^?1·min^?1) and Nicotineamide adenine dinucleotide-dichlorophenol indophenol (NADH-DCIP) reductase (8.9 ??mol·mg protein^?1·min^?1) have been observed in the crude cell extracts of S. cohnii. The decolorization products of ARB were analyzed by HPLC-MS, and the results indicated the reductive pathway was responsible for azo dye decolorization by S. cohnii.     

Decolorisation of Acid Blue 74 by ultraviolet/H<Subscript>2</Subscript>O<Subscript>2</Subscript>

The photodegradation of Acid blue 74 in aqueous solution employing a H₂O₂/ultraviolet system in a photochemical reactor was investigated. The kinetics of decolorization were studied by application of a kinetic model. The results show that the reaction of decolorization followed pseudo-first order kinetics. We demonstrate that there is an optimum H₂O₂ concentration, at which the rate of the decolorization reaction is maximum. Irradiation at 253.7 nm of the dye solution in the presence of H₂O₂ results in complete discoloration after ten minutes of treatment.     

铁屑法处理含染料废水中铁屑表面化学研究

采用扫描电镜和X射线光电子能谱技术对铁屑法处理含染料废水中铁屑反应前后的表面进行了研究,结果表明：铁屑表面主要由Fe,C,O,S,Si以及其它构成铸铁的微量元素等组成．铁屑表面快速氧化是染料脱色的关键和前提步骤,铁屑表面铁的羟基氧化物增多是铁屑失活的重要原因．超声方法是铁屑再生方法之一,铸铁中的硫有助于染料脱色．     

活性艳红X-3B的厌氧生物降解与机理

以活性艳红X-3B(RBR)为研究对象,分3个不同浓度组研究其在厌氧颗粒污泥作用下的降解性能,并采用生物降解动力学方程拟合其降解过程,同时利用GC-MS分析RBR的生物降解途径.试验结果表明,RBR在厌氧颗粒污泥中降解性能很好,去除率可达93.67%,且其降解过程符合二级反应动力学,其半衰期约为3.561 h.从GC-MS和UV-可见光谱的分析得出,RBR在厌氧颗粒污泥的作用下偶氮键断裂,且生成的芳香胺类化合物进一步降解为小分子的烃类、酚类、醇类和脂类化合物.     

新生MnO2对直接染料废水的脱色作用

以化学法合成的新生MnO2作吸附剂，对直接桃红12B（Direct red 12B)，直接大红4B（Direct reb 4B)，直接耐晒蓝B2RL（Direct Fast blue B2RL)染料废水进行脱色研究，探讨了影响吸附的因素，结果表明：新生MnO2对三种染料的吸附符合Langmuir吸附等温式，吸附速率大，在适宜条件下对直接桃红，直接大红，直接耐晒蓝的脱色率分别为95．5％，96．2％和98．9％。     

高锰酸钾对染料废水的脱色研究

研究了影响高锰酸钾对染料废水脱色的有关因素,结果表明,脱色反应的最佳ＰＨ值应小于１．５,高锰酸钾的浓度对脱色效果显著。     

氮源及其添加模式对钝齿棒杆菌JDN28-75合成L-精氨酸的影响

氮源是微生物过量合成L-精氨酸的重要营养因子之一,不同氮源对钝齿棒杆菌JDN28-75合成L-精氨酸的影响研究结果表明,硫酸铵为合适的氮源.不同初始硫酸铵浓度对JDN28-75产L-精氨酸的影响研究结果表明,氮源浓度过高或不足,都会使最终L-精氨酸产量有所降低.低浓度的硫酸铵虽然有利于菌体生长,但对L-精氨酸的合成明显不利,同时糖酸转化率也较低;而高浓度的硫酸铵尽管不利于细胞的生长且造成发酵结束时残糖含量过高,却有利于细胞合成L-精氨酸且实际耗糖的糖酸转化率维持在一个较高的水平.初始硫酸铵浓度为60 g/L时,对JDN28-75菌体的生长有明显的抑制作用,最终发酵液中剩余的硫酸铵也较多(大于30 g/L),但高浓度的硫酸铵是L-精氨酸合成所必需的.在上述研究结果的基础上,确定了初始硫酸铵浓度为20 g/L条件下的补氮策略,比较了4种不同的硫酸铵补加模式对产L-精氨酸的影响,结果表明,在总的硫酸铵浓度相同的情况下,采取分批、低浓度添加氮源的方式既可以有效解除发酵前期高浓度硫酸铵对菌体生长的抑制作用,又可以有效维持发酵中后期体系中菌体合成L-精氨酸所需的较高比例的氮源.最后,在5 L全自动发酵罐中采用20 g/L的初始硫酸铵浓度,连续流加25%的氨水来控制发酵体系pH及补加氮源,L-精氨酸的产量可以达到31.7 g/L,较对照组的产酸量(26.0 g/L)提高了21.9%.图4表2参11     

JAZ型絮凝剂对活性染料的絮凝效果

本文介绍了新近开发的ＪＡＺ絮凝凝剂地水样中活性艳红Ｋ－２ＢＰ，活性紫Ｈ－２Ｒ和活性黑Ｋ－ＢＲ染料的絮凝效果及ＰＨ值和投药比对脱色率的影响。在中性和弱酸性中絮凝效果好。投药比增大脱色率增加。对活性艳红和活性紫，起始浓度增加则达到８８．５％脱色率的投药比降低。对三种活性染料配水和活性 染料配水和活性黑染料生产水脱色率均可达到９９％，处理液残余色度在２０倍以下。