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Decolorization of reactive brilliant red K-2BP by white rot fungus under sterile and non-sterile conditions 被引量:3
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作者 GAO Da-wen WEN Xiang-hua QIAN Yi 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2006年第3期428-432,共5页
Almost all the studies both domestic and international using white rot fungus for dye wastewater treatment are performed under sterile conditions. However, it is obviously unpractical that wastewater with dyes is trea... Almost all the studies both domestic and international using white rot fungus for dye wastewater treatment are performed under sterile conditions. However, it is obviously unpractical that wastewater with dyes is treated under sterile conditions. A feasible study was made for using white rot fungus Phanerochaete chrysosporium to degrade reactive brilliant red K-2BP dye under non-sterile conditions. The results showed that there was no decolorizing effect under non-sterile condition if white rot fungus was incubated under non-sterile condition, and the decolorization was always near to 0% during decolorizing test for 3 d; in the meantime, a lot of yeast funguses were found in liquid medium when white rot fungus was incubated under non-sterile conditions; however, if white rot fungus was incubated under sterile condition firstly, its decolorization was above 90% under non-sterile condition, which was similar to that of sterile condition. So we point out that the treating process for wastewater with dyes should be divided into two stages. The first stage is that white rot fungus should be incubated under sterile conditions, and the second stage is that reactive brilliant red K-2BP is decolorized under non-sterile conditions. The method not only save the operation cost which decolorizing reactive brilliant red K-2BP under sterile condition, but also provide the feasibility for using white rot fungus to degrade wastewater with dyes under non-sterile conditions. 展开更多
关键词 white rot fungus Phanerochaete chrysosporium reactive brilliant red k-2BP DECOLORIZATION non-sterile condition
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新生MnO_2对水中活性艳红K-2G的脱色作用研究 被引量:3
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作者 马子川 蒋兰宏 +2 位作者 张素坤 霍庆 董丽丽 《重庆环境科学》 北大核心 2002年第1期29-31,共3页
以化学法合成的新生 Mn O2 作吸附剂 ,对水中活性艳红 K- 2 G进行吸附脱色研究 ,探讨了影响吸附的因素和吸附机理。结果表明 :新生 Mn O2 对活性艳红 K- 2 G的吸附符合 L angmuir吸附等温式 ,吸附前溶液 p H值是影响染料脱色效果的最主... 以化学法合成的新生 Mn O2 作吸附剂 ,对水中活性艳红 K- 2 G进行吸附脱色研究 ,探讨了影响吸附的因素和吸附机理。结果表明 :新生 Mn O2 对活性艳红 K- 2 G的吸附符合 L angmuir吸附等温式 ,吸附前溶液 p H值是影响染料脱色效果的最主要因素 ,染料浓度、Mn O2 投加量和温度影响程度较小。在实验条件下可使活性艳红 K- 2 G的脱色率高达 96 % 展开更多
关键词 新生MNO2 活性艳红k-2g 吸附作用 脱色 二氧化锰 废水处理 染料 吸附剂
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TiO_2光催化分解酸性红G和活性艳红K-2G的研究 被引量:3
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作者 张会芳 文晨 耿信鹏 《化工技术与开发》 CAS 2004年第1期33-35,共3页
研究了在紫外光的照射下 ,由 Ti O2 催化分解染料酸性红 G和活性艳红 K- 2 G的行为 ,并且探讨了 Ti O2的添加量、染料结构、染料的初始浓度以及溶液 p H值等因素对上述 2种染料光催化分解的影响。实验结果表明 ,当Ti O2 的添加量为 3g&#... 研究了在紫外光的照射下 ,由 Ti O2 催化分解染料酸性红 G和活性艳红 K- 2 G的行为 ,并且探讨了 Ti O2的添加量、染料结构、染料的初始浓度以及溶液 p H值等因素对上述 2种染料光催化分解的影响。实验结果表明 ,当Ti O2 的添加量为 3g· L- 1时 ,2种染料的催化分解率最大 ;在碱性条件下 (p H=8.5 )的分解效果好于酸性条件 (p H=5 .5 ) 展开更多
关键词 TIO2 酸性红g 活性艳红k-2g 废水处理 光催化分解
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ZnO-CeO_(2)/g-C_(3)N_(4)三元复合催化剂的制备及其对活性红195的光催化降解性能 被引量:1
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作者 沈拥军 范凯霞 +3 位作者 陈银 房帅康 徐浩 王煊轩 《化工环保》 CAS CSCD 北大核心 2023年第2期234-240,共7页
采用热聚合法和水热法制备了ZnO-CeO_(2)/g-C_(3)N_(4)三元复合催化剂,并以活性红195为目标污染物进行了光催化降解实验。表征结果显示,CeO_(2)和ZnO被成功负载到g-C_(3)N_(4)表面。实验结果表明:当Ce(NO_(3))_(3)·6H_(2)O投加量为... 采用热聚合法和水热法制备了ZnO-CeO_(2)/g-C_(3)N_(4)三元复合催化剂,并以活性红195为目标污染物进行了光催化降解实验。表征结果显示,CeO_(2)和ZnO被成功负载到g-C_(3)N_(4)表面。实验结果表明:当Ce(NO_(3))_(3)·6H_(2)O投加量为0.11 g时制备的催化剂光催化性能最佳,紫外光下反应60 min活性红195的去除率可达91.7%,优于CeO_(2)/g-C_(3)N_(4);酸性条件有利于活性红195的降解,最佳溶液pH为3.0。ZnO-CeO_(2)/g-C_(3)N_(4)三元复合材料中任意两种组分之间带隙错开,形成了Ⅱ型异质结构,增强了光生电子-空穴的分离效率,可诱导更多的活性物质参与光降解过程。 展开更多
关键词 ZnO-CeO_(2)/g-C_(3)N_(4) 三元催化剂 光催化 活性红195 水热法
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Preparation of TiO_2/activated carbon with Fe ions doping photocatalyst and its application to photocatalytic degradation of reactive brilliant red K2G 被引量:4
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作者 LI YouJi,LI Jing,MA MingYuan,OUYANG YuZhu & YAN WenBin College of Chemistry and Chemical Engineering,Jishou University,Jishou 416000,China 《Science China Chemistry》 SCIE EI CAS 2009年第8期1113-1119,共7页
Titanium dioxide coated on activated carbon(AC) with Fe ions doping(Fe-TiO2/AC) composite was prepared by an improved sol-gel method.The photocatalytic activities were tested by photocatalytic degradation of reactive ... Titanium dioxide coated on activated carbon(AC) with Fe ions doping(Fe-TiO2/AC) composite was prepared by an improved sol-gel method.The photocatalytic activities were tested by photocatalytic degradation of reactive brilliant red K2G in solution.The results show that in comparison with the agglomeration of pure TiO2,the TiO2 nanoparticles are well dispersed in the AC matrix,of which sizes are decreased with Fe ions doping.Additionally,the iron species on TiO2 of composite are Fe2O3 and FeO,which do not affect the crystalline structures of TiO2 nanoparticles.The AC matrix and iron doping content influence the fluorescence intensity of composite due to their effects on recombination probability of hole-electron pairs.Compared with TiO2,0.3% Fe-TiO2,TiO2/AC,0.5% Fe-TiO2/AC and 0.1% Fe-TiO2/AC,the 0.3% Fe-TiO2/AC shows the highest photoactivity with the complete mineralization of K2G for finite time due to the optimum Fe ions content and AC matrix.Furthermore,the kinetic constant(k=0.0229 min-1) of 0.3% Fe-TiO2/AC composite is more than the sum of both TiO2/AC(0.0154 min-1) and 0.3% Fe-TiO2(0.0057 min-1) because coexistence of the AC and Fe ions has an enlarging effect on improving the photoactivity of TiO2. 展开更多
关键词 TiO2 nanoparticles FE IONS activated carbon photocatalysis reactive brilliant red K2g
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Electrochemical degradation of reactive brilliant red X-3B with the(CeO_2/C)-β-PbO_2-PTFE composite electrode 被引量:2
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作者 孙鹏哲 陈东辉 《Journal of Rare Earths》 SCIE EI CAS CSCD 2016年第5期507-520,共14页
The(CeO2/C)-β-PbO2-PTFE composite electrodes modified by graphite powder,cerium oxide powder,polytetrafluoroethylene(PTFE)and the homemade β-PbO2 powder were prepared by the high pressure molding technique.The X... The(CeO2/C)-β-PbO2-PTFE composite electrodes modified by graphite powder,cerium oxide powder,polytetrafluoroethylene(PTFE)and the homemade β-PbO2 powder were prepared by the high pressure molding technique.The X-ray diffraction(XRD)was used to test the purity of the homemade β-PbO2 powder.The surface structure and electrical property of electrodes were characterized by using scanning electron microscopy(SEM)and the cyclic voltammetry curves(CV).Those images indicated that in electrolysis the(CeO2/C)-β-PbO2-PTFE composite electrodes had higher activity than the β-PbO2-PTFE electrodes,as good as the excellent catalytic performance.In the electrode system the composite electrodes were applied to treat reactive brilliant red(RBR)X-3B solution and we studied the degradation influence factors and the reaction mechanism.The results showed that the electrode system was well in treating RBR X-3B solution with the 20%(CeO2/C)-β-PbO2-PTFE composite electrodes at the initial 100 mg/L RBR X-3B concentration,Na2SO4 concentration of 0.35 mol/L,the constant current density of 30 mA/cm~!2 and electrolyte pH =2.After electrolytic time of 90 min,the maximum decolorization and chemical oxygen demand(COD)removal rates reached 88.92% and 54.54%.And the decolorization rate of RBR X-3B was in conformity with pseudo-first-order kinetics equation.The RBR X-3B degradation mechanism in the electrochemical oxidation system was used with LC-MS to analyze the possible intermediates and degradation pathway. 展开更多
关键词 CeO2 PbO2 reactive brilliant red X-3B chemical oxygen demand decolorization rare earths
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响应面法优化等离子体掺氮改性TiO_(2)纳米管的制备条件 被引量:5
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作者 李艳 《应用化工》 CAS CSCD 北大核心 2022年第2期466-470,共5页
采用响应面法对等离子体掺氮TiO_(2)纳米管(N-TiO_(2))的制备条件进行优化,获得具有高光电催化活性的催化剂。以活性艳红K-2BP为目标降解物,分别对掺氮功率、掺氮时间及外加偏压进行单因素实验,并采用Design-Expert8.0软件设计响应面实... 采用响应面法对等离子体掺氮TiO_(2)纳米管(N-TiO_(2))的制备条件进行优化,获得具有高光电催化活性的催化剂。以活性艳红K-2BP为目标降解物,分别对掺氮功率、掺氮时间及外加偏压进行单因素实验,并采用Design-Expert8.0软件设计响应面实验,构建响应面模型,然后对结果进行ANOVO、等高线与三维曲线分析。结果表明,掺氮功率为10 W,掺氮时间为90 s,外加偏压为20 V时,N-TiO_(2)纳米管光电催化活性最佳;经验证,该条件下的响应目标模型的预测值与实验值的误差率仅为0.79%,N-TiO_(2)纳米管带隙明显减小。 展开更多
关键词 等离子体 N-TiO_(2)纳米管 光电催化 响应面 活性艳红k-2BP
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掺铜TiO_2光催化降解活性艳红X-3B的研究 被引量:5
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作者 林雨露 《江汉大学学报(自然科学版)》 2009年第1期37-40,共4页
采用溶胶-凝胶法制备掺铜TiO2光催化剂,以活性艳红X-3B溶液光催化降解反应为模型,研究各种因素对活性艳红X-3B光催化降解的影响.实验结果表明:适量的Cu2+掺杂可明显提高TiO2的活性,本实验中最佳量为0.5%.掺杂Cu2+的TiO2光催化剂最佳用量... 采用溶胶-凝胶法制备掺铜TiO2光催化剂,以活性艳红X-3B溶液光催化降解反应为模型,研究各种因素对活性艳红X-3B光催化降解的影响.实验结果表明:适量的Cu2+掺杂可明显提高TiO2的活性,本实验中最佳量为0.5%.掺杂Cu2+的TiO2光催化剂最佳用量为1.5g/L,溶液pH为5左右,活性艳红X-3B溶液初始浓度为40mg/L,加入H2O21ml/L,40min左右活性艳红X-3B降解率可达到94.3%. 展开更多
关键词 掺铜TiO2 光催化降解 活性艳红X-3B
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UV/Mn^(2+)协同催化H_2O_2降解染料X-3B的动力学研究
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作者 李琴 楼朝刚 +2 位作者 成功 夏东升 曾庆福 《工业用水与废水》 CAS 2009年第5期24-27,共4页
研究了初始pH值、溶解氧、H2O2浓度及水中常见阴离子对UV/Mn2+协同催化H2O2降解活性艳红X-3B动力学的影响。结果表明,UV/Mn2+协同催化H2O2能有效地降解染料X-3B;在通入空气0.5L/min、pH值为4、H2O2浓度为10mmol/L的条件下,有利于UV/Mn2+... 研究了初始pH值、溶解氧、H2O2浓度及水中常见阴离子对UV/Mn2+协同催化H2O2降解活性艳红X-3B动力学的影响。结果表明,UV/Mn2+协同催化H2O2能有效地降解染料X-3B;在通入空气0.5L/min、pH值为4、H2O2浓度为10mmol/L的条件下,有利于UV/Mn2+对H2O2的协同催化,提高反应速率;NO3-、SO42-及Cl-等阴离子对X-3B的降解具有抑制作用,其中NO3-的抑制途径是阻碍紫外线透过溶液,而SO42-及Cl-则是直接和溶液中·OH反应产生抑制作用。SO42-及Cl-的抑制作用随着离子浓度的升高而增强,但NO3-的抑制强弱和离子浓度大小无关。 展开更多
关键词 UV/Mn2+ 协同催化 H2O2 活性艳红X-3B 动力学
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蒽醌-2-磺酸盐强化电辅助微生物体系对偶氮染料的脱色效果 被引量:5
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作者 张明慧 曹占平 李松松 《环境科学研究》 EI CAS CSCD 北大核心 2017年第3期471-477,共7页
为了提高微生物对偶氮染料的降解效率,将电辅助引入微生物还原降解过程,对比研究了EAMS(电辅助微生物体系)、ECS(电化学体系)和MS(微生物体系)对偶氮染料活性艳红X-3B的降解效果,并考察了不同摩尔浓度的AQS(蒽醌-2-磺酸盐)对电微生物体... 为了提高微生物对偶氮染料的降解效率,将电辅助引入微生物还原降解过程,对比研究了EAMS(电辅助微生物体系)、ECS(电化学体系)和MS(微生物体系)对偶氮染料活性艳红X-3B的降解效果,并考察了不同摩尔浓度的AQS(蒽醌-2-磺酸盐)对电微生物体系降解染料的强化作用.结果表明:反应24 h时,EAMS对活性艳红X-3B的去除率达到99.8%,比MS(去除率为61.9%)和ECS(去除率为27.1%)二者之和还要大10.8%;EAMS对活性艳红X-3B的降解过程符合一级反应动力学特征.当c(AQS)为0.050 mmol/L时,降解最快,一级动力学常数为1.962 h^(-1),是未添加AQS(0.264 4 h^(-1))的7.42倍.加入AQS后,体系中电流升高,说明AQS加快了降解过程中电子传递速率.研究显示,AQS的加入实现了电极-远离电极的微生物-染料之间多相反应界面远程电子传递过程,使整个体系的微生物都可以快速发挥作用,达到强化降解偶氮染料. 展开更多
关键词 电辅助微生物 活性艳红X-3B 反应动力学 蒽醌-2-磺酸盐 远程电子传递
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聚乙烯亚胺氨基化改性聚偏氟乙烯接枝丙烯酸纤维膜对活性艳红X-3B的吸附研究 被引量:2
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作者 常会 范文娟 《冶金分析》 CAS 北大核心 2020年第3期16-24,共9页
以丙烯酸(AA)为接枝单体,通过溶液聚合法在聚偏氟乙烯(PVDF)上接枝AA,制备出PVDF-g-PAA共聚物,再使用聚乙烯亚胺(PEI)对PVDF-g-PAA进行氨基化改性,制备出PEI氨基化PVDF-g-PAA共聚物(PEI-PVDF-g-PAA),再通过静电纺丝法制备出PEI-PVDF-g-... 以丙烯酸(AA)为接枝单体,通过溶液聚合法在聚偏氟乙烯(PVDF)上接枝AA,制备出PVDF-g-PAA共聚物,再使用聚乙烯亚胺(PEI)对PVDF-g-PAA进行氨基化改性,制备出PEI氨基化PVDF-g-PAA共聚物(PEI-PVDF-g-PAA),再通过静电纺丝法制备出PEI-PVDF-g-PAA纤维膜。使用扫描电子显微镜对PEI-PVDF-g-PAA纤维膜的微观结构进行表征,结果显示纤维膜中纤维的直径为30~50 nm,表面有丰富的微孔。以PEI-PVDF-g-PAA纤维膜为吸附材料对模拟活性艳红X-3B染料废水进行吸附,并研究其吸附动力学、吸附等温模型和吸附热力学,结果表明:PEI-PVDF-g-PAA纤维膜的吸附效果远远大于纯PVDF纤维膜和PVDF-g-PAA纤维膜。在活性艳红X-3B溶液的初始质量浓度为150 mg/L、pH=1、吸附材料用量为0.015 g时,吸附70 min后达到平衡,平衡吸附量为494.95 mg/g,PEI-PVDF-g-PAA纤维膜对活性艳红X-3B的吸附过程满足拟二级动力学模型和Langmuir吸附等温模型,说明PEI-PVDF-g-PAA纤维膜对活性艳红X-3B的吸附是以化学吸附为主的单分子层吸附,理论平衡吸附量和理论饱和吸附量分别为526.32 mg/g和500.00 mg/g。吸附热力学研究表明,PEI-PVDF-g-PAA纤维膜对活性艳红X-3B的吸附是自发进行的吸热反应,该吸附过程固-液界面的熵值会增加。 展开更多
关键词 PEI-PVDF-g-PAA纤维膜 活性艳红X-3B 吸附 静电纺丝
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A simple and cheap method for preparation of coupled ZrO_(2)/ZnO with high photocatalytic activities
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作者 WANG Zheng ZHANG Bingru LI Fengting 《Frontiers of Environmental Science & Engineering》 SCIE EI CSCD 2007年第4期454-458,共5页
The objective of this study was to prepare a new photocatalyst with high activities for degradation of organic pollutants.Coupled ZrO_(2)/ZnO photocatalyst was prepared with a simple precipitation method with cheap ra... The objective of this study was to prepare a new photocatalyst with high activities for degradation of organic pollutants.Coupled ZrO_(2)/ZnO photocatalyst was prepared with a simple precipitation method with cheap raw materials zinc acetate and zirconium oxychloride,and was character-ized by X-ray diffraction(XRD)and transmission electron microscopy(TEM).Reactive brilliant red X-3B was used as a model compound to investigate the photocatalytic activity of synthesized catalysts in water under 254 nm UV irradia-tion.Results show that the optimal calcination temperature and coupling molar ratio of Zr were 350°C and 2.5%,respec-tively.At the calcination temperature of 350°C,ZrO_(2) was dispersed on the surface of hexagonal ZnO in the form of amorphous clusters.The particle size of ZrO_(2)/ZnO decreased with the decrease of calcination temperature and the increase of Zr coupling amount.ZrO_(2)/ZnO has better photocatalytic activity for degradation of reactive brilliant red(RBR)X-3B than pure ZnO and P25-TiO_(2). 展开更多
关键词 COUPLED ZrO_(2)/ZnO PHOTOCATALYTIC activity reactive brilliant red X-3B P25-TiO_(2)
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