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CeO_(2)形貌对Ru/CeO_(2)液相催化还原N-二甲基亚硝胺的影响

Effect of CeO_(2) morphology on Ru/CeO_(2) for liquid phase catalytic reduction of N-nitrosodimethylamine
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摘要 采用3种不同形貌的氧化铈(立方体c-CeO_(2)、棒状r-CeO_(2)与八面体o-CeO_(2))为载体,采用沉淀沉积法制备了Ru/CeO_(2)催化剂,并研究了水中N-二甲基亚硝胺(NDMA)的催化加氢还原反应.结果表明,3种催化剂的NDMA还原活性顺序为Ru/c-CeO_(2)>Ru/o-CeO_(2)>Ru/r-CeO_(2).XPS、拉曼等表征结果显示,Ru/c-CeO_(2)具有较高的Run+和适量的氧空位含量,其金属-载体相互作用最强,具有最高的还原活性.NDMA液相催化还原反应符合朗格缪尔-欣谢尔伍德模型,NDMA在催化表面的吸附是反应的控制步骤.催化剂对NDMA催化还原效率随着pH的升高呈倒火山型变化.催化剂经过5次循环利用后,仍有较好的催化活性. Ru/CeO_(2) catalysts were prepared by precipitation deposition method using three ceria oxides with different morphologies(cubic-CeO_(2),rod-CeO_(2) and octahedral-CeO_(2))as supports,and the catalytic hydrogenation reduction of N-dimethylnitrosamine(NDMA)was studied in water.The results show that the removal efficiency of NDMA on the three catalysts follows Ru/c-CeO_(2)>Ru/o-CeO_(2)>Ru/r-CeO_(2).The characterization results of XPS and Raman show that Ru/c-CeO_(2) has higher Run+and appropriate oxygen vacancy content,which has stronger metal support interaction and higher reduction activity than other catalysts.The NDMA liquid phase catalytic reduction reaction conforms to the Langmuir-Hinshelwood model,and the conversion of adsorbed NDMA on the catalytic surface is the rate-determining step.The liquid phase catalytic reduction of N-nitrosodimethylamine on Ru/CeO_(2) shows an inverted volcanic change with the increase of pH.The catalyst still has good catalytic activity after five cycles.
作者 信晋凯 孙玉菡 余乐 郑寿荣 许昭怡 XIN Jinkai;SUN Yuhan;YU Le;ZHENG Shourong;XU Zhaoyi(State Key Laboratory of Pollution Control and Resource Reuse Research,College of the Environment,Nanjing University,Nanjing,210023,China)
出处 《环境化学》 CAS CSCD 北大核心 2024年第11期3788-3797,共10页 Environmental Chemistry
基金 国家自然科学基金(21976086)资助.
关键词 液相催化加氢 N-二甲基亚硝胺(NDMA) Ru/CeO_(2) 金属-载体相互作用 liquid phase catalytic hydrogenation N-nitrosodimethylamine Ru/CeO_(2) metal-support interaction
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  • 1Gunten Ursvon, Hoigne Jurg. Bromate formation during ozonation of bromide-containing waters: Interaction of ozone and Hydroxyl Radical reactions [J]. Environmental Science and Technology, 1994,28:1234-1242.
  • 2Ratpukdi Thunyalux, Casey Francis, Thomas Desutter, et al. Bromate formation by ozone-VUV in comparison with ozone and ozone-UV: effects of pH, ozone dose, and VUV power [J]. Journal of environmental engineering, 2011, 5:187-195.
  • 3Chen Huan, Xu Zhaoyi, Wan Haiqin, et al. Aqueous bromate reduction by catalytic hydrogenation over Pd/Al2O3 catalysts [J]. Applied Catalysis B: Environmental, 2010,96:307-313.
  • 4Wang Qiliang, Snyder Shane, Kim Jungwoo, et al. Aqueous ethanol modified nanoscale zerovalent iron in bromate reduction: synthesis, characterization, and reactivity [J]. Environmental Science and Technology, 2009,43:3292-3299.
  • 5Li Xie, Shang Chii. Effects of copper and palladium on the reduction of bromate by Fe(0) [J]. Chemosphere, 2006,64:919- 930.
  • 6Wisniewski Jacek A, Kabsch-korbutowicz Malgorzata. Bromate removal in the ion-exchange process [J]. Desalination, 2010,261: 197-201.
  • 7Kishimoto Naoyuki, Matsuda Nobuaki, et al. Bromate ion removal by electrochemical reduction using an activated carbon felt electrode [J]. Environmental Science and Technology, 2009, 43:2054-2059.
  • 8Huang Winnjung, Cheng Yungling. Effect of characteristics of activated carbon on removal of bromate [J]. Separation and Purification Technology, 2008,59:101-107.
  • 9Paschoal Fabiana Maria Monteiro, Pepping Greg, Zanoni Maria Valniee Boldrin, et al. Photoelectrocatalytic removal of bromate using Ti/TiO2 coated as a photoeathode [J]. Environmental Science and Technology, 2009,43:7496 7502.
  • 10Xu Zhaoyi, Chen Liqiang, Shao Yun, et al. Catalytic Hydrogenation of Aqueous Nitrate over Pd-Cu/ZrO2 Catalysts [J]. Industrial and Engineering Chemistry Research, 2009,48:8356- 8363.

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