沈阳化工大学学报
瀋暘化工大學學報
침양화공대학학보
JOURNAL OF SHENYANG INSTITUTE OF CHEMICAL TECHNOLOGY
2012年
1期
26-30
,共5页
姬生菲%申延明%刘东斌%徐世博
姬生菲%申延明%劉東斌%徐世博
희생비%신연명%류동빈%서세박
碳纳米管%Pd/CNTs催化剂%苯酚%环己酮%加氢反应
碳納米管%Pd/CNTs催化劑%苯酚%環己酮%加氫反應
탄납미관%Pd/CNTs최화제%분분%배기동%가경반응
carbon nanotube%Pd/CNTs catalyst%phenol%cyclohexanone%hydrogenation
通过对纳米碳管进行纯化、表面修饰处理,浸渍PdCl2溶液制得Pd/CNTs催化剂,进行化学组成及XRD表征,测试Pd/CNTs催化剂对苯酚气相加氢制环己酮的催化性能.实验结果表明:Pd负载到CNTs上,负载量为0.97%(质量分数),负载后的碳纳米管仍然保留碳纳米管的结构.Pd/CNTs催化性能测试结果表明:反应温度为150℃,氢酚摩尔比4∶1,液体进料速率0.42 mL/g.h的条件下催化剂活性较好,此时苯酚转化率43.17%,环己酮选择性达68.36%.
通過對納米碳管進行純化、錶麵脩飾處理,浸漬PdCl2溶液製得Pd/CNTs催化劑,進行化學組成及XRD錶徵,測試Pd/CNTs催化劑對苯酚氣相加氫製環己酮的催化性能.實驗結果錶明:Pd負載到CNTs上,負載量為0.97%(質量分數),負載後的碳納米管仍然保留碳納米管的結構.Pd/CNTs催化性能測試結果錶明:反應溫度為150℃,氫酚摩爾比4∶1,液體進料速率0.42 mL/g.h的條件下催化劑活性較好,此時苯酚轉化率43.17%,環己酮選擇性達68.36%.
통과대납미탄관진행순화、표면수식처리,침지PdCl2용액제득Pd/CNTs최화제,진행화학조성급XRD표정,측시Pd/CNTs최화제대분분기상가경제배기동적최화성능.실험결과표명:Pd부재도CNTs상,부재량위0.97%(질량분수),부재후적탄납미관잉연보류탄납미관적결구.Pd/CNTs최화성능측시결과표명:반응온도위150℃,경분마이비4∶1,액체진료속솔0.42 mL/g.h적조건하최화제활성교호,차시분분전화솔43.17%,배기동선택성체68.36%.
Pd/CNTs was prepared by impregnation with PdCl2 and carbon nanotubes (CNTs).Before impregnation,CNTs were purified and modified using H2SO4 and HNO3.The resulted Pd/CNTs was characterized by ultraviolet spectrophotometry and XRD.It was showed that Pd was loaded on the CNTs and its content was 0.97 %.The structure of CNTs was kept its original structure.It was indicated that the better catalytic performance of Pd/CNTs was obtained under the following conditions:reaction temperature was 150 ℃,the molar ratio of H2 to phenol was 4 and the feed rate was 0.42 mL/g·h.The phenol conversion of 43.17 % and cyclohexanone selectivity of 68.36 % was obtained under the above condition.