Chaffin KA, Knutsen JS, Brant P, Bates FS
Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN 55455, USA. Exxon Chemical Company, Baytown Polymers Center, Baytown, TX 77522, USA.
Science. 2000 Jun 23;288(5474):2187-90. doi: 10.1126/science.288.5474.2187.
Spectacular advances in organometallic chemistry over the past two decades have resulted in single-site catalysts that are revolutionizing production of polyethylene (PE) and isotactic polypropylene (iPP). This report describes an unanticipated benefit of metallocene-catalyzed semicrystalline polyolefins, namely welded joint strengths in PE/iPP laminates that can exceed the cohesive strength of the constituents. We propose that interfacial polymer entanglements, established in the molten state and subsequently anchored in chain-folded lamellae upon crystallization, are responsible for this intrinsic property. The poor adhesion exhibited by traditional Ziegler-Natta-catalyzed polyolefins is shown to derive from the accumulation of amorphous polymer, a by-product of the polymerization reactions, at the interface. These results should facilitate fabrication and improve the properties of composites based on materials that dominate the plastics industry.
在过去二十年中,有机金属化学取得了惊人的进展,催生出了单中心催化剂,这些催化剂正在彻底改变聚乙烯(PE)和全同立构聚丙烯(iPP)的生产方式。本报告描述了茂金属催化的半结晶聚烯烃一个意想不到的优点,即在PE/iPP层压板中的焊接接头强度可以超过组分的内聚强度。我们认为,在熔融状态下形成并在结晶时随后锚定在链折叠片晶中的界面聚合物缠结是造成这种固有特性的原因。传统齐格勒-纳塔催化的聚烯烃表现出的较差粘附性被证明是由于聚合反应的副产物无定形聚合物在界面处的积累所致。这些结果应有助于基于主导塑料行业的材料制造复合材料并改善其性能。