催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2014年
6期
914-921
,共8页
吴树昌%温国栋%钟炳伟%张炳森%谷献模%王宁%苏党生
吳樹昌%溫國棟%鐘炳偉%張炳森%穀獻模%王寧%囌黨生
오수창%온국동%종병위%장병삼%곡헌모%왕저%소당생
碳材料%氧官能团%活性位%硝基苯%还原
碳材料%氧官能糰%活性位%硝基苯%還原
탄재료%양관능단%활성위%초기분%환원
Carbon materials%Oxygenated groups%Active sites%Nitrobenzene%Reduction
本文对碳材料(主要是碳纳米管)催化硝基苯的还原反应进行了系统研究。通过热重分析、程序升温脱附、透射电子显微镜、物理吸附以及拉曼光谱等表征,发现碳材料表面的含氧官能团在反应中起着重要的作用,而比表面、孔结构、形貌、结构缺陷以及可能存在的铁杂质对反应没有显著影响。羰基的作用非常重要,但是羧基和酸酐对反应不利。除此之外,材料的π电子体系也很关键,因为它可以传递电子,并且利于硝基苯的吸附。硝基苯还原按照直接路径进行,反应过程中生成的中间体亚硝基苯可以迅速转化为苯胺。
本文對碳材料(主要是碳納米管)催化硝基苯的還原反應進行瞭繫統研究。通過熱重分析、程序升溫脫附、透射電子顯微鏡、物理吸附以及拉曼光譜等錶徵,髮現碳材料錶麵的含氧官能糰在反應中起著重要的作用,而比錶麵、孔結構、形貌、結構缺陷以及可能存在的鐵雜質對反應沒有顯著影響。羰基的作用非常重要,但是羧基和痠酐對反應不利。除此之外,材料的π電子體繫也很關鍵,因為它可以傳遞電子,併且利于硝基苯的吸附。硝基苯還原按照直接路徑進行,反應過程中生成的中間體亞硝基苯可以迅速轉化為苯胺。
본문대탄재료(주요시탄납미관)최화초기분적환원반응진행료계통연구。통과열중분석、정서승온탈부、투사전자현미경、물리흡부이급랍만광보등표정,발현탄재료표면적함양관능단재반응중기착중요적작용,이비표면、공결구、형모、결구결함이급가능존재적철잡질대반응몰유현저영향。탄기적작용비상중요,단시최기화산항대반응불리。제차지외,재료적π전자체계야흔관건,인위타가이전체전자,병차리우초기분적흡부。초기분환원안조직접로경진행,반응과정중생성적중간체아초기분가이신속전화위분알。
The reduction of nitrobenzene catalyzed by different carbon materials (mainly carbon nanotubes) was studied. TGA, TPD, TEM, N2 adsorption-desorption, and Raman spectroscopy were used to show that it was oxygenated groups that gave catalytic activity, while the surface area, pore struc-ture, morphology, structural defects and Fe impurities in the catalysts did not have a significant influence on the activity. The carbonyl group played an important role, but the carboxylic group and anhydride adversely affected the reaction. The conjugated π system, which was necessary for elec-tron transfer and nitrobenzene adsorption, was another critical factor. The reaction proceeded through the direct route in which the intermediate nitrosobenzene was converted directly to aniline quickly.