Visualization of on-surface ethylene polymerization through ethylene insertion

Author:

Guo Weijun12ORCID,Yin Junqing3ORCID,Xu Zhen2ORCID,Li Wentao2ORCID,Peng Zhantao2ORCID,Weststrate C. J.4,Yu Xin1ORCID,He Yurong3,Cao Zhi13ORCID,Wen Xiaodong13ORCID,Yang Yong3,Wu Kai2ORCID,Li Yongwang13,Niemantsverdriet J. W.14ORCID,Zhou Xiong12ORCID

Affiliation:

1. SynCat@Beijing, Synfuels China Technology Co., Ltd., Beijing 101407, China.

2. Beijing National Laboratory for Molecular Sciences (BNLMS), College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.

3. State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.

4. SynCat@DIFFER, Syngaschem BV, 5600 HH Eindhoven, Netherlands.

Abstract

Polyethylene production through catalytic ethylene polymerization is one of the most common processes in the chemical industry. The popular Cossee-Arlman mechanism hypothesizes that the ethylene be directly inserted into the metal–carbon bond during chain growth, which has been awaiting microscopic and spatiotemporal experimental confirmation. Here, we report an in situ visualization of ethylene polymerization by scanning tunneling microscopy on a carburized iron single-crystal surface. We observed that ethylene polymerization proceeds on a specific triangular iron site at the boundary between two carbide domains. Without an activator, an intermediate, attributed to surface-anchored ethylidene (CHCH 3 ), serves as the chain initiator (self-initiation), which subsequently grows by ethylene insertion. Our finding provides direct experimental evidence of the ethylene polymerization pathway at the molecular level.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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