Synergistic binding sites in a hybrid ultramicroporous material for one-step ethylene purification from ternary C2hydrocarbon mixtures

Author:

Zhang Peixin12ORCID,Zhong Yao1ORCID,Zhang Yan3ORCID,Zhu Zhenliang1,Liu Yuan1,Su Yun1,Chen Jingwen1,Chen Shixia1ORCID,Zeng Zheling1ORCID,Xing Huabin2ORCID,Deng Shuguang4,Wang Jun1ORCID

Affiliation:

1. Chemistry and Chemical Engineering School, Nanchang University, Nanchang 330031, P.R. China.

2. Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, P.R. China.

3. Jiangxi University of Chinese Medicine, Nanchang, 330031, Jiangxi, P.R. China.

4. School for Engineering of Matter, Transport and Energy, Arizona State University, 551 E. Tyler Mall, Tempe, AZ 85287, USA.

Abstract

One-step separation of C2H4from ternary C2H2/C2H4/C2H6hydrocarbon mixtures is of great significance in the industry but is challenging due to the similar sizes and physical properties of C2H2, C2H4, and C2H6. Here, we report an anion-pillared hybrid ultramicroporous material, CuTiF6-TPPY, that has the ability of selective recognition of C2H4over C2H2and C2H6. The 4,6-connectedfscframework of CuTiF6-TPPY exhibits semi–cage-like one-dimensional channels sustained by porphyrin rings and TiF62−pillars, which demonstrates the noticeably enhanced adsorption of C2H2and C2H6over C2H4. Dynamic breakthrough experiments confirm the direct and facile high-purity C2H4(>99.9%) production from a ternary gas mixture of C2H2/C2H6/C2H4(1/9/90, v/v/v) under ambient conditions. Computational studies and in situ infrared reveal that the porphyrin moieties with large π-surfaces form multiple van der Waals interactions with C2H6; meanwhile, the polar TiF62−pillars form C–H•••F hydrogen bonding with C2H2. In contrast, the recognition sites for C2H4in the framework are less marked.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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