期刊文献+

微孔树脂镶嵌超细α-Fe_2O_3催化剂的制备、表征及其在苯酚H_2O_2羟化制备苯二酚反应中的应用 被引量:3

Preparation and Characterization of Nanoscales α-Fe_2O_3/Microporous resin Catalyst and the Application in Hydroxylation of Phenol with H 2O 2 to Dihydroxybenzene
在线阅读 下载PDF
导出
摘要 用离子交换方法制备了 α-Fe2 O3/微孔树脂催化剂 .XRD,TEM和 Mossbauer谱测试结果表明 ,制得的α-Fe2 O3粒子尺寸非常细小 ,其粒径至少在 5 nm以下 .该催化剂在苯酚 H2 O2 羟化制备苯二酚反应中表现出了良好的催化活性 ,在 n(苯酚 ) / n( H2 O2 ) =3条件下 ,苯酚的有效转化率可达到 2 2 .4 % ,产物中邻苯二酚和对苯二酚的物质的量比接近 1 .4∶ 1 ,反应放大 30 0 0倍后羟化活性及产物的选择性基本不变 .与化学沉淀法制得的纳米 α-Fe2 O3羟化活性比较认为 ,造成二者催化活性不同的主要原因是 α-Fe2 The nanoscales α Fe 2O 3 /microporous resin catalyst was prepared by the ion exchange method and characterized by means of X ray diffraction(XRD), transmission electron microscopy(TEM) and Mssbauer spectroscopy. The uses of these techniques make it possible to perform an estimation of the size of the iron oxide crystallites on microporous resin. The size of the crystallites has been found to be smaller than 5 nm. The catalyst prepared exhibited a very good catalytic activity on the hydroxylation of phenol with H 2O 2 to dihydroxybenzene. The effect conversion of phenol reached 22.4% when phenol/H 2O 2(molar ratio) is 3 and the ratio of catechol and hydroquinone is about 1.4 in the products. The results didnt change when the reaction was magnified to 3 000 times. Furthermore, compared α Fe 2O 3 /microporous resin with α Fe 2O 3 prepared from chemical precipitation, it was thought that the reason of different hydroxylation activity of phenol between the two kinds of catalysts was the size of particles in nature.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2002年第2期259-262,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金 (批准号 :2 97730 16 )资助
关键词 Α-FE2O3 微孔树脂 苯酚 过氧化氢 羟化 苯二酚 催化剂 表征 α-三氧化二铁 催化活性 Fe 2O 3/microporous resin Phenol Hydroxylation with H 2O 2 Dihydroxybenzene
  • 相关文献

参考文献2

二级参考文献7

共引文献48

同被引文献51

  • 1于剑锋,杨宇,吴通好,孙家锺.Dawson结构钼钒磷杂多化合物对苯酚过氧化氢羟化作用的研究[J].高等学校化学学报,1996,17(1):126-128. 被引量:22
  • 2崔作林 张志焜.纳米技术与纳米材料[M].北京:国防工业出版社,2000..
  • 3YU W Y , LIU H F, TAO Q. Modification of metal cations to metal cluster in liquid medium [J]. Chem Commun. 1996,1773 - 1774.
  • 4FENG H, LIU H F. The metal complex effect on metal clusters in liquid medium[J]. J Mol Catal A , 1997,126 (1) :5 -8.
  • 5YING J Y, TSCHOPE A, LEVIN D. Synergistic effects and catalytic properties tailored by nanostructure processing[ J]. Nanostructured Materials, 1995,6 : 237 - 246.
  • 6DENG H M, DING J. Ultrafine zinc oxide powers prepared by precipitation mechanical milling[J]. Journal of Materials Science, 2001, (13) :3273 -3276.
  • 7CAPEK I, JURANICOVA V. Emulsion polymerization of unsatured monomers in the presence of inorganinc ultrafine particles[J]. Chimecal Papers, 1994, (3) :155 -161.
  • 8BROTONS V, COQ B, PLANEIX J M. Catalytic influence of bimetallic phases for the synthesis of single walled carbonnanotubes[J]. J Mol Catal A: Chemical, 1997, 116: 397.
  • 9LAMBERT J M, AJAYAN P M, BERNIER P. Improving conditions towards isolating single shell carbon nanotubes [ J ].Chem Phys Lett, 1994, 226: 364.
  • 10ATSUSHI Fukuoka, NAONORI Higashimoto, YUZURU Sakamoto, et al. Ship - in - bottle synthesis and catalytic performances of platinum carbonyl clusters, nanowires, and nanoparticles in micro - and mesoporous materials[ J]. Catalysis Today,2001, 66:23 -31.

引证文献3

二级引证文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部