脱氢
化学
催化作用
聚烯烃
开裂
烯烃纤维
沸石
氢
石油化工
化学工程
有机化学
聚乙烯
铂金
金属
杂质
废物管理
除氧
磷化物
精细化工
废物流
贵金属
贵金属
催化裂化
催化加氢
氢气储存
化学反应
水分
烷烃
微型多孔材料
原材料
作者
L Y H Sun,Xiaomei Wang,Jing Xu,Meng Zhao,Shuyan Song,Hongjie Zhang,Xiao Wang
摘要
Hydrocracking is a significant chemical route for recycling waste plastic. Utilizing inexpensive crude hydrogen to drive this reaction offers substantial economic benefits. However, CO, the primary impurity in crude hydrogen, readily poisons the metal sites, leading to catalyst deactivation. Herein, we report a CO-tolerant catalytic system constructed by blending silicalite-1 zeolite (S1)-encapsulated Pt-Ni binary metals with Ce-modified HY zeolite, which possesses exceptional capability for converting polyethylene into C3-C5 products. For comparison, the monometallic counterparts based on either Pt or Ni manifest pronounced deactivation under the same conditions. Sequential investigations reveal that this catalytic system follows a "two-way compensation" mechanism. In the presence of CO, Pt experiences a loss of hydrogenation activity while retaining its dehydrogenation capability. Conversely, Ni loses its dehydrogenation ability but maintains its hydrogenation capacity. The synergistic combination of Ni and Pt effectively compensates for each other's functional shortcomings, ensuring the seamless progression of the hydrogenation reaction.
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