催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2014年
4期
546-552
,共7页
任世彪%宏志%曹先中%王知彩%雷智平%潘春秀%康士刚%水恒福
任世彪%宏誌%曹先中%王知綵%雷智平%潘春秀%康士剛%水恆福
임세표%굉지%조선중%왕지채%뢰지평%반춘수%강사강%수항복
镍%有机蒙脱石%高活性%萘%加氢
鎳%有機矇脫石%高活性%萘%加氫
얼%유궤몽탈석%고활성%내%가경
Nickel Organic montmorillonite%High activity%Naphthalene%Hydrogenation
以有机改性后的十六烷基三甲基溴化铵柱撑蒙脱石(CTAB-MMT)为载体,采用浸渍法制备了Ni/MMT催化剂.通过傅里叶红外光谱、X射线衍射、H2程序升温脱附、N2物理吸附以及紫外漫散射等物理化学手段对催化剂进行了表征;并结合微型高压反应釜萘加氢反应,评价了催化剂的加氢性能.结果表明,有机改性显著改善了Ni/MMT催化剂的金属Ni分散度和织构性质,且所制催化剂表现出优异的萘加氢性能, Ni萘转化率达到88.2%,不仅远高于未处理催化剂(13.1%)和Al2O3柱撑处理催化剂(24.2%),而且高于Ni/SBA-15催化剂(68.2%).鉴于CTAB有机柱撑体在催化剂还原过程因热解而消除,其对催化剂所起的作用主要发生于浸渍过程,提出了有机改性在浸渍过程对Ni/MMT催化剂的促进作用机制.
以有機改性後的十六烷基三甲基溴化銨柱撐矇脫石(CTAB-MMT)為載體,採用浸漬法製備瞭Ni/MMT催化劑.通過傅裏葉紅外光譜、X射線衍射、H2程序升溫脫附、N2物理吸附以及紫外漫散射等物理化學手段對催化劑進行瞭錶徵;併結閤微型高壓反應釜萘加氫反應,評價瞭催化劑的加氫性能.結果錶明,有機改性顯著改善瞭Ni/MMT催化劑的金屬Ni分散度和織構性質,且所製催化劑錶現齣優異的萘加氫性能, Ni萘轉化率達到88.2%,不僅遠高于未處理催化劑(13.1%)和Al2O3柱撐處理催化劑(24.2%),而且高于Ni/SBA-15催化劑(68.2%).鑒于CTAB有機柱撐體在催化劑還原過程因熱解而消除,其對催化劑所起的作用主要髮生于浸漬過程,提齣瞭有機改性在浸漬過程對Ni/MMT催化劑的促進作用機製.
이유궤개성후적십륙완기삼갑기추화안주탱몽탈석(CTAB-MMT)위재체,채용침지법제비료Ni/MMT최화제.통과부리협홍외광보、X사선연사、H2정서승온탈부、N2물리흡부이급자외만산사등물이화학수단대최화제진행료표정;병결합미형고압반응부내가경반응,평개료최화제적가경성능.결과표명,유궤개성현저개선료Ni/MMT최화제적금속Ni분산도화직구성질,차소제최화제표현출우이적내가경성능, Ni내전화솔체도88.2%,불부원고우미처리최화제(13.1%)화Al2O3주탱처리최화제(24.2%),이차고우Ni/SBA-15최화제(68.2%).감우CTAB유궤주탱체재최화제환원과정인열해이소제,기대최화제소기적작용주요발생우침지과정,제출료유궤개성재침지과정대Ni/MMT최화제적촉진작용궤제.
A Ni/montmorillonite (MMT) catalyst was prepared by an impregnation method using cetyltrime-thylammonium bromide (CTAB)-pillared MMT as the supporting matrix and was characterized using infrared spectroscopy, X-ray diffraction, H2 temperature-programmed desorption, N2 adsorp-tion-desorption, and ultraviolet diffuse reflectance spectroscopy. The catalytic activity of the Ni/MMT for the hydrogenation of naphthalene was also evaluated. The results show that the organ-ic modification of MMT greatly improved the Ni dispersion and textural properties of the Ni/MMT catalyst. The as-prepared Ni/MMT catalyst showed high naphthalene conversion (88.2%) in the hydrogenation reaction; this is much higher than those achieved using Ni supported on pristine MMT (13.1%), Al2O3-pillared MMT (24.2%), and SBA-15 (68.2%). As a result of thermal decomposi-tion of CTAB pillars during reduction of the Ni/MMT catalyst, the CTAB pillars mainly play a role in the Ni/MMT catalyst during impregnation. A mechanism for the promotion of the Ni/MMT catalytic activity by organic modification during impregnation is proposed.