石油化工高等学校学报
石油化工高等學校學報
석유화공고등학교학보
JOURNAL OF PETROCHEMICAL UNIVERSITIES
2001年
1期
6-9
,共4页
牛玉舒%李保山%全明秀%胡壮麒
牛玉舒%李保山%全明秀%鬍壯麒
우옥서%리보산%전명수%호장기
发泡金属%非晶态合金%苯加氢%催化剂
髮泡金屬%非晶態閤金%苯加氫%催化劑
발포금속%비정태합금%분가경%최화제
采用新型发泡非晶态Ni-P合金催化剂,在微型固定床连续反应器上进行了苯加氢制 备环己烷的实验研究。结果表明:这种新型发泡非晶态合金催化剂具有较好的加氢催化活性 和很好的选择性,在体系氢压为2.0 MPa、反应温度为300 ℃,苯的进料速率为3 mL/h的条 件下 ,环己烷的单程收率为33.28%。试验考察了该催化剂的稳定性,结果表明,在360 h内,其 催化 活性没有显著变化。另外,该催化剂具有很好的通透性,催化剂层前、后几乎无压差。试验 还发现,该催化剂没有明显的诱导期,无需经过预处理就有很好的加氢催化活性。因此,发 泡非晶态Ni-P催化剂有希望成为工业催化剂。
採用新型髮泡非晶態Ni-P閤金催化劑,在微型固定床連續反應器上進行瞭苯加氫製 備環己烷的實驗研究。結果錶明:這種新型髮泡非晶態閤金催化劑具有較好的加氫催化活性 和很好的選擇性,在體繫氫壓為2.0 MPa、反應溫度為300 ℃,苯的進料速率為3 mL/h的條 件下 ,環己烷的單程收率為33.28%。試驗攷察瞭該催化劑的穩定性,結果錶明,在360 h內,其 催化 活性沒有顯著變化。另外,該催化劑具有很好的通透性,催化劑層前、後幾乎無壓差。試驗 還髮現,該催化劑沒有明顯的誘導期,無需經過預處理就有很好的加氫催化活性。因此,髮 泡非晶態Ni-P催化劑有希望成為工業催化劑。
채용신형발포비정태Ni-P합금최화제,재미형고정상련속반응기상진행료분가경제 비배기완적실험연구。결과표명:저충신형발포비정태합금최화제구유교호적가경최화활성 화흔호적선택성,재체계경압위2.0 MPa、반응온도위300 ℃,분적진료속솔위3 mL/h적조 건하 ,배기완적단정수솔위33.28%。시험고찰료해최화제적은정성,결과표명,재360 h내,기 최화 활성몰유현저변화。령외,해최화제구유흔호적통투성,최화제층전、후궤호무압차。시험 환발현,해최화제몰유명현적유도기,무수경과예처리취유흔호적가경최화활성。인차,발 포비정태Ni-P최화제유희망성위공업최화제。
Using the novel foamed amorphous alloy-fo amed Ni-P alloy-as catal yst, the hydrogenation of benzene to cyclohexane was carried out in a minisize c atena fix-bed reactor. The products were analyzed by gas chromatograph. Through t he experiments, the suitable processing conditions were obtained as the followi ng:the re action temperature 300 ℃, the feed rate 3 mL/h and the pressure of the system 2 .0 MPa. Under these conditions, the selectivity of hexamethylene alkyl was nearl y 1 00 % and the yield was about 33.28%. The results of the research on the stability indicated that the activity didn't change much in 360 h. In addition, the catal y st has no obvious inducement time. It has a good hydrogenation activity dispense with pretreatment. So the foamed Ni-P amorphous alloy can be used as industry cata lyst.