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固体超强酸S_2O_8^(2-)/TiO_2-ZrO_2催化合成三氟甲基硝基苯 被引量:2

Synthesis of nitrotrifluorobenzene by solid superacid catalyst S_2O_8^(2-)/TiO_2-ZrO_2
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摘要 以固体超强酸S2O82-/TiO2-ZrO2为催化剂,浓硝酸为硝化剂对三氟甲苯进行硝化,考察催化剂的制备条件对催化活性的影响,以及反应时间、催化剂用量等因素对硝化反应的影响.结果表明:将TiO2-ZrO2用0.75 mol/L(NH4)2S2O8溶液浸泡12 h,并在600℃条件下焙烧3 h,可得到较高的催化活性;当固体超强酸催化剂S2O82-/TiO2-ZrO2用量为三氟甲苯质量的15%,反应4 h,三氟甲苯的转化率可达68.7%以上;催化剂具有较好的重复使用性能. The nitration of benzotrifluorede using solid superacid S2O8^2-/TiO2-ZrO2 as catalyst and nitric acid as nitrating agent was studied,the effects of preparation condition of catalyst on catalytic activity and reaction time,amount of catalyst S2O8^2-/TiO2-ZrO2 on the nitrating yield were investigated.The results showed that the S2O8^2-/TiO2-ZrO2 catalyst prepared with the concentration of(NH4)2S2O8 by 0.75 mol/L and the calcinated at 600 ℃ for 3 h,the catalytic activity of catalyst was the highest;It was founded that the nitrating yield could may up to 68.7% when amount of S2O8^2-/TiO2-ZrO2 is 15% of reactant and reaction time is 4 h;The catalyst has good reusability.
出处 《湖北大学学报(自然科学版)》 CAS 北大核心 2010年第2期175-177,201,共4页 Journal of Hubei University:Natural Science
基金 武汉市教育局项目(200771)资助
关键词 固体超强酸S2O82-/TiO2-ZrO2 三氟甲基硝基苯 三氟甲苯 硝化 solid superacid S2O8^2-/TiO2-ZrO2 nitrotrifluorobenzene benzotrifluorede nitrating
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  • 1赵璧英,马华容,唐有祺.制备方法对MoO_3/ZrO_2结构的影响及MoO_3/ZrO_2固体超强酸的结构特征 Ⅱ.活性组分存在形态的研究[J].Chinese Journal of Catalysis,1995,16(3):177-182. 被引量:26
  • 2许丹倩.间三氟甲基苯胺综述[J].浙江化工,1996,27(1):10-12. 被引量:15
  • 3化工部农药信息总站.国外农药品种手册[Z].,1996..
  • 4Sato H, Nagai K, Yoshioka H,et al. Vapor phase nitration of benzene over solid acid catalysts Ⅲ. nitration with nitric acid (2); mixed metal oxide treated with sulfuric acid and heteropolyacid partially neutralized[J]. Applied Catalysis A:General,1998,175: 209-213.
  • 5Smith K,Musson A, Deboos G A. A novel method for the nitration of simple aromatic compounds[J]. J.Org.Chem.,1998,63: 8448-8454.
  • 6Francis J W, Anthony G M B, D.Christopher Braddock,et al. Hafnium(Ⅳ) and zirconium(Ⅳ) triflates as auperior recyclable catalysts for the atom economic nitration o-nitrotoluene[J]. Tetrahedron Letters,1998,39: 1641-1642.
  • 7Landau M V, Kogan S B, Tavor D,et al. Selectivity in heterogeneous catalytic processes[J]. Catalysis Today,1997,36: 497-510.
  • 8CA71:123889
  • 9John D. Roberts, et al. Orientation in aminations of substituted halobenzenes. J.Am. Chem. Soc., 1956,78:611~14
  • 10O. Naumann et al. Trifluoromethylation of aromatic amines and thiols bybis(trifluoromethyl) telluride. Zh. Org. Khim, 1993, 1:152~55

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