化学分析计量
化學分析計量
화학분석계량
CHEMICAL ANALYSIS AND METERAGE
2014年
5期
91-94
,共4页
邵鸿飞%冀克俭%刘元俊%邓卫华%赵晓刚%高岩立%周彤%李艳玲
邵鴻飛%冀剋儉%劉元俊%鄧衛華%趙曉剛%高巖立%週彤%李豔玲
소홍비%기극검%류원준%산위화%조효강%고암립%주동%리염령
铂%钯%催化剂%制备%一氧化碳%催化活性
鉑%鈀%催化劑%製備%一氧化碳%催化活性
박%파%최화제%제비%일양화탄%최화활성
Pt%Pd%catalyst%preparation%CO%catalytic activity
用浸渍法分别将铂、钯负载在铝柱撑蒙脱石载体上,制备了铂、钯负载铝柱撑蒙脱石催化剂。运用X射线衍射(XRD)、原子吸收光谱(AAS)、透射电镜(TEM)等分析方法对样品的性能和结构进行了表征,并考察了不同铂、钯负载量的催化剂对一氧化碳的催化氧化性能。结果表明,铂、钯均以高度分散的纳米粒子状态均匀分布在载体表面,并表现出良好的CO催化氧化活性。铂、钯在铝柱撑蒙脱石载体表面的有效负载率在70%~76%之间,在相同的设计负载量条件下,铂的实际负载量和有效负载率均略大于钯。CO催化氧化试验结果表明,相对于负载前,负载后催化剂的催化活性明显增加,且其催化活性随着铂、钯负载量的增加而不断增强。在相同温度和负载量条件下,钯负载型催化剂的催化活性明显高于铂负载型催化剂。
用浸漬法分彆將鉑、鈀負載在鋁柱撐矇脫石載體上,製備瞭鉑、鈀負載鋁柱撐矇脫石催化劑。運用X射線衍射(XRD)、原子吸收光譜(AAS)、透射電鏡(TEM)等分析方法對樣品的性能和結構進行瞭錶徵,併攷察瞭不同鉑、鈀負載量的催化劑對一氧化碳的催化氧化性能。結果錶明,鉑、鈀均以高度分散的納米粒子狀態均勻分佈在載體錶麵,併錶現齣良好的CO催化氧化活性。鉑、鈀在鋁柱撐矇脫石載體錶麵的有效負載率在70%~76%之間,在相同的設計負載量條件下,鉑的實際負載量和有效負載率均略大于鈀。CO催化氧化試驗結果錶明,相對于負載前,負載後催化劑的催化活性明顯增加,且其催化活性隨著鉑、鈀負載量的增加而不斷增彊。在相同溫度和負載量條件下,鈀負載型催化劑的催化活性明顯高于鉑負載型催化劑。
용침지법분별장박、파부재재려주탱몽탈석재체상,제비료박、파부재려주탱몽탈석최화제。운용X사선연사(XRD)、원자흡수광보(AAS)、투사전경(TEM)등분석방법대양품적성능화결구진행료표정,병고찰료불동박、파부재량적최화제대일양화탄적최화양화성능。결과표명,박、파균이고도분산적납미입자상태균균분포재재체표면,병표현출량호적CO최화양화활성。박、파재려주탱몽탈석재체표면적유효부재솔재70%~76%지간,재상동적설계부재량조건하,박적실제부재량화유효부재솔균략대우파。CO최화양화시험결과표명,상대우부재전,부재후최화제적최화활성명현증가,차기최화활성수착박、파부재량적증가이불단증강。재상동온도화부재량조건하,파부재형최화제적최화활성명현고우박부재형최화제。
Pt-supported Al Pillared Montmorillonite and Pd-supported Al Pillared Montmorillonite were prepared by impregnation method. By using X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), and transmission electron microscopy (TEM), properties and structure of samples were characterized. CO catalytic oxidation performance of different deposition of Pt or Pd were investigated. The results showed that Pt or Pd showed good catalytic activity on CO oxidation in a highly dispersed state of uniform distribution on Al Pillared Montmorillonite carrier. Platinum or palladium on Al Pillared Montmorillonite carrier had effective load rate of 70%-76%. Under the same amount of design load conditions, the actual load amount and effective load rate of platinum was slightly more than that of palladium. By experimental results of CO catalytic oxidation compared with that before-loading, catalytic activity of the after-loading catalysts was significantly inproved and increased. Under the condition of same temperature and deposition, catalytic activity of Pd-supported catalyst was significantly higher than that of Pt-supported catalyst.