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羟基自由基对多壁碳纳米管表面和结构的影响 被引量:12

Effect of Hydroxyl Radical on the Surface and Structure of Multi-walled Carbon Nanotubes
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摘要 碳纳米管纯化后,使用Fenton试剂产生羟基自由基对碳管进行改性处理,研究羟基自由基对碳管表面和结构的影响,并与碳管的混酸处理结果进行比较。FTIR结果表明:经Fenton试剂化学处理后,碳管表面主要引入羟基和羰基,而混酸能“剪切”碳管,产生大量羧基和羰基等官能团。根据Fenton试剂产生羟基自由基的机理,分析了Fenton试剂处理条件的影响因素,控制反应条件即过氧化氢与亚铁离子物质的量之比保持在10左右,而pH值则维持在3左右,对碳管进行改性处理。依据碳管Fenton试剂处理前后的FTIR谱图变化,初步探讨了羟基自由基与多壁碳纳米管作用的可能机理。机理分析表明,改性后碳管表面的羟基和羰基是羟基自由基对碳管上的不饱和键进行加成氧化的结果。 After purification pretreatment by thermal oxidation and concentrated HCl, multi-walled carbon nanotubes (MWNTs) was treated with Fenton's reagents and concentrated H2SO4/HNO3 mixture, respectively. The results of FTIR spectra showed that hydroxyl groups and carbonyl groups could be brought into the MWNTs after Fenton chemical treatment. However, both carbonyl groups and carboxylic groups could be produced at broken sites when MWNTs was treated by concentrated H2SO4/HNO3 mixture. According to formation mechanisms of hydroxyl radical, the conditions of Fenton treatment were controlled: molar ratio of H2O2 and Fe2+ was 10 or so, pH was at around 3 under acidic condition. In addition, we discussed the probable mechanisms of reaction between hydroxyl radical and MWNTs by IR spectral changes before and after Fenton treatment. The probable mechanisms indicated that existence of hydroxyl groups and carbonyl groups could be viewed as outcome of addition and oxidation reaction of electrophilic hydroxyl radical on unsaturated bonds on the sidewalls of MWNTs.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2005年第2期186-190,共5页 Chinese Journal of Inorganic Chemistry
基金 上海纳米科技专项基金资助项目(No.0252nm011)
关键词 多壁碳纳米管 羟基自由基 FENTON试剂 机理 multi-walled carbon nanotubes hydroxyl radical Fenton's reagents mechanisms
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  • 1Iijima S. Nature, 1991,354(6348):56-58.
  • 2Postma H W C, Teepen T, Yao Z, et al. Science, 2001,293(5527):76-79.
  • 3Ajayan P M, Schadler L S, Giannaris C, et al. Adv. Mater,2000,12(10):750-753.
  • 4Chen P, Wu X, Lin J, et al. Science, 1999,285(5424):91-93.
  • 5LIU Lu—Qi(刘璐琪),GUO Zhi—xin(郭志新),DAI Li—Ming(戴黎明),et a1.Kexue rongbao(Chinese Science Bulletin).2001,46(19):1590-1596.
  • 6ZHU Wei—Hong(朱为宏),ZHU Shi—Qin(朱世琴),TIAN He(田禾).Youji Huaxue(Chinese J.Org.Chem.)2002.22.(12):964-973.
  • 7Ying Y M,Saini R K,Liang F,et a1.Org.Lett..2003.5(91:147l-1473.
  • 8Umek P,Seo J W,Hemadi K.et a1.Chem.Mater:.2003.15(25):475 1-4755.
  • 9PENG Feng(彭峰),JIANG Jing—Wen(姜靖雯).WANG Hong—Juan(王红娟),et a1.Wuji Huaxue Xuebao(Chinese J.Inorg.Chem.),2004,20(2):23l-234.
  • 10ZOU Hong—Ling(邹红玲),YANG Yan—Lian(杨延莲),WU Bin(武斌),et a1.Wuli Huaxue.Xuebao(Acta Phys—Chim. Sin.),2002,18(5):409-413.

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