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Degradation of Cyanide using Stabilized S, N-TiO2 Nanoparticles by Visible and Sun Light 可见光和太阳光下稳定S, N-TiO2纳米颗粒降解氰化物的研究
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0101
F. Mohammadi-Moghadam, M. Sadeghi, Neda Masoudipour
In this paper, cyanide degradation (at pH12) using S, N-TiO2 photo-catalyst, synthesized by sol-gel method, stabilizedon glass microbeads and scoria stones were investigated. The main raw materials were thiourea (Tu) as a source of S and N and tetra butyl orthotitanate (TBOT). The effects of S and N amount, visible and sun light, irradiation time and different initial cyanide concentrations (50, 100, 200 and 300 mg/L) on destruction of cyanide were studied. The S, N-TiO2 film with 0.25 g thiourea showed the best cyanide destruction in visible light. The results showed that cyanide (50 mg/L) was destructed up to 94% in visible light and approximately 100% in sun light by S, N-TiO2/glass microbead. The results also indicated 85% and 94% destruction in visible and sun light respectively by S, N-TiO2/scoria stone within 4 h. Finally, the S, N-TiO2 stabilized on glass microbeads can be effectively implemented as a new method for treatment of wastewater containing free cyanide under sun light.
本文研究了溶胶-凝胶法合成的S, N-TiO2光催化剂、稳定玻璃微珠和矿渣石在pH12下对氰化物的降解。主要原料为硫脲(Tu)和正钛酸四丁酯(TBOT)。研究了S和N用量、可见光和日光、照射时间以及不同初始氰化物浓度(50、100、200和300 mg/L)对氰化物破坏的影响。添加0.25 g硫脲的S, N-TiO2薄膜在可见光下氰化物破坏效果最好。结果表明,S, N-TiO2/玻璃微珠对氰化物(50 mg/L)在可见光下的破坏率高达94%,在太阳光下的破坏率约为100%。结果表明,S, N-TiO2/矿渣石在4 h内对可见光和日光的破坏率分别为85%和94%。最后,S, N-TiO2稳定在玻璃微珠上,可以作为一种处理日光下含游离氰化物废水的新方法有效实现。
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引用次数: 8
Oxidation Removal of Lignin-degradation Products by Zero-valent iron Activated Persulfate 零价铁活化过硫酸盐氧化脱除木质素降解产物
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2016.0158
Junjun Zhu, Lu Wu, Ya-Qian Rong, Linli Shi, Liwei Chen, Yong Xu, Q. Yong, Shiyuan Yu
A total of nine major lignin-degradation products were selected in this study for oxidation removal by a new detoxification technology-advanced oxidation process of zero-valent iron (ZVI) activated persulfate (PS). This procedure attempts to determine the effect of lignin-degradation products on ethanol fermentation during the bioethanol production process. Results indicate that the optimal oxidation conditions were pH5.0, 25°C, ZVI concentration of 1.0 g/L, and PS concentration of 1.5 g/L based on 0.1 g/L vanillin as the model of the lignin-degradation products. The oxidation effect of the eight other major lignindegradation products on the optimal conditions was also studied. Results show that their oxidation removal efficiency values were remarkable. Except for vanillin (99%), vanillic acid (97%), 4-hydroxybenzaldehyde (93%), and 4-hydroxybenzoic acid (81%), the removal efficiencies values of the five other lignin-degradation products (i.e., syringaldehyde, syringic acid, 3,4dihydroxybenzoic acid, p-coumaric acid, and ferulic acid) were all 100%. The dominant active species during the advanced oxidation process was sulfate radicals. Therefore, the ZVI/PS system is a suitable approach for the oxidation removal of lignindegradation products.
本研究选择了9种主要的木质素降解产物,采用一种新的脱毒技术——零价铁(ZVI)活化过硫酸盐(PS)氧化法进行氧化脱除。本程序试图确定在生物乙醇生产过程中木质素降解产物对乙醇发酵的影响。结果表明,以0.1 g/L香兰素为模型,木质素降解产物的最佳氧化条件为pH5.0, 25℃,ZVI浓度1.0 g/L, PS浓度1.5 g/L。研究了其他8种主要木质素降解产物在最佳条件下的氧化效果。结果表明,它们的氧化去除率显著。除香兰素(99%)、香草酸(97%)、4-羟基苯甲醛(93%)和4-羟基苯甲酸(81%)外,其余5种木质素降解产物丁香醛、丁香酸、3,4二羟基苯甲酸、对香豆酸和阿魏酸的去除率均为100%。在深度氧化过程中,主要活性物质为硫酸盐自由基。因此,ZVI/PS体系是氧化脱除木质素降解产物的理想途径。
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引用次数: 5
Effect of A Constant Electric Field on the Structure of the Oxide Layer Formed During Zinc Oxidation by Supercritical H2O and H2O/CO2 Fluids 恒定电场对超临界H2O和H2O/CO2流体氧化锌过程中氧化层结构的影响
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/jaots.2017.0049
A. Shishkin, M. Sokol, D. Dubov, O. N. Fedyaeva
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引用次数: 0
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 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
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0022
I. O. Brahim, M. Belmedani, A. Haddad, H. Hadoun, A. Belgacem
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.
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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引用次数: 3
Correlation of Surface Area with Photocatalytic Activity of TiO2 TiO2的表面积与光催化活性的关系
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0063
A. Vorontsov, E. N. Kabachkov, I. L. Balikhin, E. N. Kurkin, V. N. Troitskii, P. Smirniotis
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引用次数: 22
Efficient Oxidative Removal of Sulfonamide Antibiotics from the Wastewater by Potassium Ferrate 高铁酸钾高效氧化去除废水中的磺胺类抗生素
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0053
Kang Wu, Huiqing Wang, Chen Zhou, Y. Amina, Y. Si
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引用次数: 8
Degradation of a Toxic Molecule o-Toluidine in Industrial Effluents using UV254/PS System UV254/PS系统降解工业废水中的有毒分子邻甲苯胺
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0099
Maya Amasha, Abbas Baalbaki, Suha Al Hakim, Rime El Asmar, A. Ghauch
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引用次数: 24
Generation of Active Chlorine in Acid and Alkaline Medium Using a 3D Anode in an Electrochemical Reactor for Reactive Black 5 Degradation 电化学反应器中三维阳极在酸碱性介质中生成活性氯的研究
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0069
Francisca A. Rodríguez, M. Cruz-Díaz, Sebastián Gómez, J. Calderon, A. Ortega, E. Rivero
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引用次数: 2
Identification of Newly Discovered Degradation Intermediates of Benzene Compounds 新发现的苯类化合物降解中间体的鉴定
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0092
Chen Wang, Anjing Wang, Ruyu Zhang, Naidong Zhang, Yujie Feng
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引用次数: 4
Synthesis of N-Doped Graphene Oxide Quantum Dots with the Internal P-N Heterojunction and Its Photocatalytic Performance under Visible Light Illumination 内P-N异质结氮掺杂氧化石墨烯量子点的合成及其在可见光下的光催化性能
Q Chemistry Pub Date : 2018-01-01 DOI: 10.26802/JAOTS.2017.0033
Weiqiang Zhang, Xiufang Zhang, Xiaoli Dong, Hongchao Ma, Guowen Wang
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引用次数: 2
期刊
Journal of Advanced Oxidation Technologies
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