光催化法降解有机废水的显著性研究

本文采用紫外光照射并加入催化剂的方法，对有机废水一阳离子艳红染料(5GN)进行了光催化降解的研究。从实际应用出发，实验得出了影响阳离子艳红染料降解的各因素的最佳取值及影响显著性次序。     

TiO2光催化降解阳离子艳红反应动力学研究

本文以沉淀法制备的TiO2为催化剂,紫外杀菌灯为光源,对阳离子艳红染料的光催化降解进行动力学研究.实验结果表明TiO2光催化降解低浓度阳离子艳红的反应为一级反应,反应动力学行为符合Langmuir-Himshelwood方程,其反应速率常数为1.87 mg/L·min.     

TiO2光催化降解有机颜料艳红RGS母液研究

以TiO2为催化剂,对有机颜料艳红RGS母液进行了一系列光催化降解试验.考察了催化剂用量、溶液pH值、初始浓度、不同光源和照射时间对脱色率的影响.结果表明,溶液相对初始浓度为0.2、pH<8、催化剂用量为1g/L时,以紫外灯(254nm)为光源,反应120 min,脱色率可达93%以上.     

阳离子染料废水治理技术

介绍了阳离子染料废水的特点，以及近年来阳离子染料废水的各种处理技术，并对阳离子染料废水处理技术的发展进行了展望，指出阳离子废水处理技术正朝着各种工艺优化组合的方向发展。     

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。     

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 )     

ClO2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,pHWFHG,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,单一染料溶液及混痊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）。     

用TiO2-Ag-改性膨润土复合催化剂光催化氧化处理染料废水

制备了一种Ti02-Ag-改性膨润土复合催化剂，用该催化剂对直接黑L-N和直接铜蓝BR染料废水进行了光催化氧化处理，取得了较好的实验效果。     

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％）。     

HPA／ZnFe2O4-TiO2光催化剂的制备及对马拉硫磷的可见光降解

以纳米TiO2载体，利用浸渍法制备了HPA／ZnFe2O4-TiO2光催化剂。对制备的催化剂进行了XRD、BET、TEM和UV-vis DRS表征。结果表明，催化剂样品均为锐钛矿相且ZnFe2O4很好地分散在载体表面，HPA／ZnFe2O4-TiO2光催化荆的平均粒径为10nm且在380-670nm均有强的光响应；反应最佳的HPA浓度为O.08molfL，最佳的ZnFe2O4负载量为1％。考察了HPA溶液初始浓度、ZnFe2O4负载量、溶液初始pH值、H2O2用量、催化剂用量对催化剂活性的影响。在溶液初始pH=13，H2O2=6mmol／L，催化剂用量为2g/L的最优条件下，光照反应进行100min后，马拉硫磷的降解率可达87％；重复4次后马拉硫磷的降解率仍可以达到67％。     

Photocatalytic degradation of disperse blue 1 using UV/TiO2/H2O2 process

The photocatalytic degradation of a dye derivative, C.I. disperse blue 1 (1), has been investigated under UV light irradiation in the presence of TiO2 and H2O2 under a variety of conditions. The degradation was studied by monitoring the change in substrate concentration employing UV spectroscopic technique as a function of irradiation time. The degradation was studied under different conditions such as different types of TiO2, reaction pH, catalyst and substrate concentration containing hydrogen peroxide (H2O2), besides molecular oxygen in the presence of TiO2. The degradation of dye was also investigated under sunlight and the efficiency of degradation was compared with that of the artificial light source. The degradation rates were found to be strongly influenced by all the above parameters. The photocatalyst Degussa P25 was found to be more efficient for the degradation of the dye.     

间接电化学降解亚甲基蓝废水的可行性研究

研究以ClO^-／Cl^-作媒介，间接电化学降解亚甲基蓝模拟废水的可行性。结果表明，亚甲基蓝的电化学降解与电极材料、电流密度以及添加剂种类等因素有关。以石墨为阳极，不锈钢为阴极，在无隔膜的烧杯中放置50ml浓度为1000mg/L的亚甲基蓝模拟废水，在室温25℃，pH6．0－8．0，槽电压10V，电流密度30．0mA/cm^2，Cl^-加入量2g/L的条件下，电解60min后，亚甲基蓝溶液的平均消色率达到98．0％，CODcr降解率为97．0％，BOD5降解率为99．0％；用浸涂过MnO2薄膜的石墨棒作阳极可显著加快其消解速率，而用浸涂过CeO2薄膜的石墨棒作阳极对其消解速率无明显的影响。并初步讨论了其降解机理。     

Visible light driven instantaneous photocatalytic degradation of aniline blue (AB) and methyl violet (MV) by strontium ferrite nanoparticles

Toxic organic dyes released into aquatic sources as a result of industrial activities pose a significant threat to the environment. The removal of such dyes from water sources is a challenging task in the context of environmental emergencies. In this present effort, the strontium ferrite nanoparticles were synthesized by coprecipitation followed by a calcination method and is applied for photocatalytic degradation of such organic dyes. The ferrite nanoparticles were characterized by FTIR, XRD, VSM, SEM-EDX, TEM, and HR-TEM studies. In the existence of H₂O₂ under visible light, the catalyst performs efficient degradation of aniline blue (AB) and methyl violet (MV) dyes in a remarkably short interval of time. The superparamagnetic performance of the catalyst was confirmed by VSM, and thus it can be easily recovered from the degraded dye by applying an external magnet. The Fenton mechanism justifies the elevated rate of photo degradation, which generates hydroxyl and perhydroxyl radicals in the progress of the reaction.     

Removal of the hazardous dye rhodamine B through photocatalytic and adsorption treatments

This paper reports on photocatalytic and adsorptive treatment of a hazardous xanthene dye, Rohdamine B, in wastewater. The photocatalytic degradation was carried out in the presence of the catalyst TiO(2) and the effects of pH, concentration of the dye, amount of TiO(2), temperature and electron acceptor H(2)O(2) on the degradation process were observed. It was found that photocatalytic degradation by TiO(2) is an effective, economical and faster mode of removing Rohdamine B from aqueous solutions. Attempts were also made to utilize activated carbon and rice husk as potential adsorbents to remove Rhodamine B from wastewater. The adsorption studies were carried out at 40, 50 and 60 degrees C, and the effects of pH, temperature, amount of adsorbents, concentration of adsorbate, etc., on the adsorption were measured. On the basis of adsorption data the Langmuir and Freundlich adsorption isotherm models were also confirmed. The adsorption isotherm constants thus obtained were employed to calculate thermodynamic parameters like Gibb's free energy, change in enthalpy and entropy. In order to observe the quality of wastewater COD measurements were also carried out before and after the treatments. A significant decrease in the COD values was observed, which clearly indicates that both photocatalytic and adsorption methods offer good potential to remove Rhodamine B from industrial effluents.     

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.     

Catalytic degradation of toxic organic dye using an aluminum-doped Cu0.4Zn0.6-xAlxFe2O4 (x = 0.0, 0.2, 0.4, 0.6) spinel ferrite in a photo-Fenton system

Catalytic activity of spinel ferrite in breaking down toxic dye materials are promising due to their uniqueness. In this study, aluminum-doped copper zinc ferrite, Cu_0.4Zn_0.6-xAl_xFe₂O₄ (x = 0.0, 0.2, 0.4, 0.6), a catalyst for toxic dye degradation is synthesized through chemical co-precipitation route. The formation of the spinel ferrite catalyst is initially confirmed by Fourier transform infrared spectra, which shows the frequency of metal-oxygen bond vibration at 539 and 427 cm⁻¹ attributed to the tetrahedral and octahedral sites respectively. Higher intensity sharp peak of X-ray diffraction for (311) plane is the evidence for the phase purity and the formation of spinel ferrite. The crystallite size is found to decrease with the increase of Al³⁺ ion. The surface structure of the obtained particles is investigated using a scanning electron microscope. Analyses of the material's magnetic characteristics using a vibrating sample magnetometer (VSM) revealed that it is, in fact, a soft magnet, as evidenced by the loop of its hysteresis, which is narrow. The catalytic degradation of methylene blue dye under the mechanism of the photo-Fenton process is studied with the obtained spinel ferrites and the result is found to be as high as 96.5%. The process follows pseudo-second order kinetics and the Langmuir isotherm.     

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%。     

光催化氧化处理低浓度含醇废水实验

室内实验了TiO2紫外光催化氧化处理废水中的低浓度甲醇。通过对TiO2催化剂活性及添加方式、溶液pH、紫外光强与催化剂加量等参数优化,在TiO2加入浓度为300mg/L和120 W紫外灯照射条件下,对6.8L甲醇浓度为2.77%的低浓度含醇废水持续处理70min后,废水中的甲醇去除率可达98.31%。该实验为进一步处理低浓度含醇废水提供了方法依据。     

Intensification of degradation of aqueous solutions of rhodamine B using sonochemical reactors at operating capacity of 7 L

In the present work, degradation of rhodamine B, a typical dye effluent commonly observed in chemical processing wastewaters has been investigated using a sonochemical reactor with capacity of 7 L. The reactor consists of an ultrasonic bath equipped with a single large transducer having longitudinal vibrations with operating frequency of 25 kHz and rated power output of 1 kW. The effect of operational conditions such as the rhodamine B initial concentration, operating pH and use of additives such as H(2)O(2), CCl(4) and TiO(2) has been investigated initially. A mathematical model has also been fitted to estimate the rate constant for rhodamine B removal under different operating conditions. Intensification studies have been carried by combining sonochemical oxidation with photocatalytic oxidation under optimized conditions. In all the investigated systems, complete removal of rhodamine B (10 ppm initial concentration) was obtained using a combination of sonochemical reactor and CCl(4). Sonocatalysis (in the presence of TiO(2)) of rhodamine B showed 92% degradation, while sonophotocatalysis gave degradation of 93%. TOC analysis at various optimum conditions was also performed to quantify the extent of mineralization and it was observed that the extent of mineralization is always lower than the extent of removal of parent compound.