Control of zeolite pore interior for chemoselective alkyne/olefin separations

Author:

Chai Yuchao1ORCID,Han Xue2ORCID,Li Weiyao2ORCID,Liu Shanshan1,Yao Sikai1,Wang Chong3,Shi Wei4ORCID,da-Silva Ivan5ORCID,Manuel Pascal5ORCID,Cheng Yongqiang6ORCID,Daemen Luke D.6,Ramirez-Cuesta Anibal J.6ORCID,Tang Chiu C.7,Jiang Ling3ORCID,Yang Sihai2ORCID,Guan Naijia14,Li Landong14ORCID

Affiliation:

1. School of Materials Science and Engineering and National Institute for Advanced Materials, Nankai University, Tianjin 300350, China.

2. Department of Chemistry, The University of Manchester, Manchester, M13 9PL, UK.

3. State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

4. Key Laboratory of Advanced Energy Materials Chemistry of Ministry of Education, Nankai University, Tianjin 300071, China.

5. ISIS Facility, Science and Technology Facilities Council (STFC), Rutherford Appleton Laboratory, Chilton, Oxfordshire, OX11 0QX, UK.

6. Neutron Scattering Division, Neutron Sciences Directorate, Oak Ridge National Laboratory (ORNL), Oak Ridge, TN 37831, USA.

7. Diamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire, OX11 0DE, UK.

Abstract

Zeolites that prefer alkynes Alkenes such as ethylene and propene must be separated from alkynes before they can be converted in polymers. Drawbacks in current methods, such as hydrogenation of alkynes producing unwanted alkanes, has spurred interest in sorption separation methods. Zeolites have generally been inefficient, given the similar sizes and volatilities of the molecules. Chai et al. incorporated atomically dispersed divalent transition metal cations into faujasite zeolite and found that the nickel-containing analog efficiently removed alkynes from olefins through chemoselective binding at open nickel(II) sites. At ambient conditions in the presence of water and carbon dioxide, the zeolites retained separation selectivities of 100 and 92, respectively, for acetylene over ethylene and propyne over propylene for 10 adsorption-desorption cycles. Science , this issue p. 1002

Funder

Royal Society

EPSRC

111 Project

National Natural Science Fund of China

Municipal Natural Science Fund of Tianjin

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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