Degradation of C.I. Acid Red 51 and C.I. Acid Blue 74 in Aqueous Solution by Combination of Hydrogen Peroxide, Nanocrystallite Zinc Oxide and Ultrasound Irradiation

I. O. Brahim, M. Belmedani, A. Haddad, H. Hadoun, A. Belgacem
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引用次数: 3

Abstract

Journal of Advanced Oxidation Technologies2018; 21(1)www.jaots.netDOI:10.26802/jaots.2017.0022Journal of Advanced Oxidation Technologies 2018; 21(1)Article ID-20170022Article:Degradation of C.I. Acid Red 51 and C.I. Acid Blue 74 in Aqueous Solution by Combination of Hydrogen Peroxide, Nanocrystallite Zinc Oxide and Ultrasound IrradiationInsaf Ould Brahim*1,3, Mohamed Belmedani1,Ahmed Haddad3, Hocine Hadoun2,Ahmed Belgacem11Laboratory of transfer phenomena, Faculty of Mechanical and Processes Engineering, University of Sciences and Technology Houari Boumediene, BP n 32 El Alia bab ezzouar 16111 Algiers, Algeria2Nuclear Research Center of Algiers, 2 Bd Frantz Fanon, 16035, Algiers, Algeria3Research Center in Industrial TechnologiesCRTI, P.O.Box 64, Cheraga 16014 Algiers, Algeria *iouldbrahim@gmail.comPhone: 00213-20-77-67Fax: 00213-21-34 -20-19AbstractThis study illustrates the degradation of food dyes, C.I. Acid Red 51 (erythrosine E127) and C.I. Acid Blue 74 (indigo carmine E132) by sonocatalysis using an ultrasonic frequency of 37 kHz and a power of 150 W in the presence of heterogeneous catalysts ZnO and peroxide hydrogen (H2O2). The adsorption process for the two dyes on the ZnO nanocrystalline which satisfies the Freundlich model appears not effective because the elimination of the two food dyes does not exceed 35%. In order to improve the removal, the sonocatalytic process (AD-OX) has been investigated. At this purpose, effect of operating parameters such as initial dye concentrations, H2O2(0-0.75M) and initial pH on the sonochemical degradation was investigated. It was observed that when the adsorption-catalysis was assisted by the ultrasonic and H2O2 a considerable yields has been achieved and about 86% and 97% of E127 and E132 were removed for 10 mg L-1and 50 mg L-1respectively. To understand the behavior of dye degradation, structure of the zinc catalyst before and after the sonocatalytic process was characterized by meanX-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM).Results showed thatthe ZnO particles before and after sonocatalysis were crystallized in the hexagonal wurtzite phase and the size distribution indicates that most of the particles are in the range of 300 and 600 nm. Finally, ADMI and COD analysis were performed in order toquantify the residual color in solution and evaluate the efficiency of the dye mineralization. Results showed that the treatment of food dyes by US-ZnO-H2O2process increased color degradation (ADMI)and mineralization efficiency (COD) by more than 50% and 76% respectively.
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双氧水、纳米晶氧化锌和超声辐照联合降解水溶液中C.I.酸红51和C.I.酸蓝74
高级氧化技术学报;2018;21(1)www.jaots.netDOI:10.26802/jaots.2017.0022;文章:过氧化氢、纳米晶氧化锌和超声辐照联合降解水溶液中C.I.酸红51和C.I.酸蓝74 [j] . Ould Brahim*1,3, Mohamed Belmedani1,Ahmed hadad3, Hocine Hadoun2,Ahmed belgacem11 .转移现象实验室,Houari Boumediene科技大学机械与工艺工程学院,BP, 32 El Alia, 16111 Algiers,2阿尔及利亚阿尔及尔核研究中心,2 bfrantz Fanon, 16035,阿尔及利亚阿尔及尔3 crti,工业技术研究中心,64号信箱,阿尔及利亚阿尔及尔16014 *iouldbrahim@gmail.comPhone: 00213-20-77-67摘要以氧化锌和过氧化氢(H2O2)为催化剂,在37 kHz、150 W的超声频率下,研究了食用染料C.I.酸红51(红素E127)和C.I.酸蓝74(靛胭脂E132)的声催化降解。在满足Freundlich模型的ZnO纳米晶上对这两种染料的吸附并不有效,因为这两种食品染料的去除率不超过35%。为了提高其去除率,对声催化(AD-OX)工艺进行了研究。为此,研究了初始染料浓度、H2O2(0-0.75M)和初始pH等操作参数对声化学降解的影响。结果表明,在超声波和H2O2辅助下,在10 mg l -1和50 mg l -1条件下,E127和E132的去除率分别为86%和97%。为了解染料降解行为,采用x射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)和扫描电镜(SEM)对声催化过程前后锌催化剂的结构进行了表征。结果表明:超声催化前后的ZnO颗粒均在六方纤锌矿相结晶,粒径分布表明,大部分ZnO颗粒在300 ~ 600 nm范围内;最后,进行ADMI和COD分析,以量化溶液中的残留颜色,并评估染料矿化效率。结果表明,采用us - zno - h2o2工艺处理食用染料,可使染料的显色降解率(ADMI)提高50%以上,矿化率(COD)提高76%以上。
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期刊介绍: The Journal of advanced oxidation technologies (AOTs) has been providing an international forum that accepts papers describing basic research and practical applications of these technologies. The Journal has been publishing articles in the form of critical reviews and research papers focused on the science and engineering of AOTs for water, air and soil treatment. Due to the enormous progress in the applications of various chemical and bio-oxidation and reduction processes, the scope of the Journal is now expanded to include submission in these areas so that high quality submission from industry would also be considered for publication. Specifically, the Journal is soliciting submission in the following areas (alphabetical order): -Advanced Oxidation Nanotechnologies -Bio-Oxidation and Reduction Processes -Catalytic Oxidation -Chemical Oxidation and Reduction Processes -Electrochemical Oxidation -Electrohydraulic Discharge, Cavitation & Sonolysis -Electron Beam & Gamma Irradiation -New Photocatalytic Materials and processes -Non-Thermal Plasma -Ozone-based AOTs -Photochemical Degradation Processes -Sub- and Supercritical Water Oxidation -TiO2 Photocatalytic Redox Processes -UV- and Solar Light-based AOTs -Water-Energy (and Food) Nexus of AOTs
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