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Polyethylene with Reverse Co‐monomer Incorporation: From an Industrial Serendipitous Discovery to Fundamental Understanding
Authors:Dimitrije Cicmil  Dr Jurjen Meeuwissen  Dr Aurélien Vantomme  Dr Jian Wang  Ilse K van?Ravenhorst  Dr Hendrik E van?der?Bij  Dr Ara Muñoz‐Murillo  Prof?Dr Bert M Weckhuysen
Institution:1. Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht (The Netherlands);2. Refining & Chemicals, Total Research and Technology Feluy, Zone Industrielle C, 7181 Seneffe (Belgium);3. Soft X‐ray Spectromicroscopy, Canadian Light Source Inc., 44 Innovation Boulevard, SK S7N 2V3 Saskatoon (Canada)
Abstract:A triethylaluminium(TEAl)‐modified Phillips ethylene polymerisation Cr/Ti/SiO2 catalyst has been developed with two distinct active regions positioned respectively in the inner core and outer shell of the catalyst particle. DRIFTS, EPR, UV‐Vis‐NIR DRS, STXM, SEM‐EDX and GPC‐IR studies revealed that the catalyst produces simultaneously two different polymers, i.e., low molecular weight linear‐chain polyethylene in the Ti‐abundant catalyst particle shell and high molecular weight short‐chain branched polyethylene in the Ti‐scarce catalyst particle core. Co‐monomers for the short‐chain branched polymer were generated in situ within the TEAl‐impregnated confined space of the Ti‐scarce catalyst particle core in close proximity to the active sites that produced the high molecular weight polymer. These results demonstrate that the catalyst particle architecture directly affects polymer composition, offering the perspective of making high‐performance polyethylene from a single reactor system using this modified Phillips catalyst.
Keywords:heterogeneous catalysis  in   situ oligomerisation  Phillips catalyst  polyethylene  scanning transmission x‐ray microscopy
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