摘要
通过(NH4)Mo7O24·4H2O和(NH4)2HPO4水溶液沉淀、焙烧在923K用H2还原制得磷化钼催化剂.XRD检测表明,用H2还原后有纯的磷化钼生成.在3.0MPa的高压连续微反系统中测定催化剂的加氢活性.以制备的磷化钼为活性组分、γ-Al2O3为稀释剂,考察了空速、反应温度和反应时间对模型化合物的HDN、HDS和HDY性能的影响,结果表明:在合适的条件下,其脱硫脱氮率可达到90%以上.模型化合物为吡啶、噻吩和环己烯,吡啶含量以N计(为0.2%)、噻吩含量以S计(为0.3%),环己烯含量为20%,以环己烷作溶剂.
A molybdenum phosphide catalyst was prepared from an aqueous solution of (NH4)6Mo7O\{24\}·4H2O and (NH4)2HPO4 by precipitation, calcination, and subsequent reduction in H2 at 923 K. XRD measurements revealed that pure molybdenum phosphide had formed after the reduction in H2. The reactivity study was carried out using 3 g catalyst in a high pressure system at 3.0 MPa. A sample of molybdenum phosphide catalyst diluted with γ\|Al2O3 was used for simultaneous HDN? HDS and HDY. The influences of space velocity, reaction temperature, reaction time on hydrotreating performance were researched. Pyridine, thiophene and cyclohexene were used as model compounds, their contents were 0.2%(N)? 0.3%(S) and 20% respectively. Cyclohexane was used as solvent.
出处
《分子催化》
EI
CAS
CSCD
北大核心
2003年第1期52-55,共4页
Journal of Molecular Catalysis(China)
基金
国家自然科学基金资助课题(20173005).
关键词
磷化钼
催化剂
加氢脱氮
加氢脱硫
加氢精制
石油工业
Molybdenum phosphide
Catalyst
Hydrodenitrogenation
Hydrodesulfurization
Hydrorefining