Polyolefins,
the largest used commodity plastics in the world,
find extensive application in many fields. However, most end up in
landfills or incineration, leading to severe ecological crises, environmental
pollution, and serious resource waste problems. As representatives
on chemical upcycling of polyolefin plastics polyolefin waste to fuels
and bulk/fine chemicals, polyolefin catalytic cracking and hydrocracking
based on zeolite or metal/zeolite composite catalysts are considered
the most effective paths due to their large capacity and strong adaptability
to existing petrochemical equipment. After an overview of the reaction
mechanisms of pyrolysis and catalytic cracking, this review aims to
comprehensively discuss the influence of zeolite catalyst structure
(acidity, pore structure, and morphology) on the catalytic activity,
selectivity, and stability of polyolefin cracking, particularly emphasizing
the importance for matching acidity and pore structure for target
product formation. Subsequently, the structure–activity relationship
between the metal site and zeolite’s acid site in polyolefin
hydrocracking is also discussed. In the end, emerging opportunities
and challenges are proposed to promote a more efficient way for polyolefin
chemical upcycling.