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Performance and mechanism of the separation of C8 α-olefin from F-T synthesis products using novel Ag-DES
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  • Hu Li,
  • Zisheng Zhang,
  • Guanlun Sun,
  • Suli Liu,
  • Liangcheng An,
  • Xingang Li,
  • Hong Li,
  • Xin Gao
Hu Li
Tianjin University

Corresponding Author:[email protected]

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Zisheng Zhang
University of Ottawa
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Guanlun Sun
Tianjin university
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Liangcheng An
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Xingang Li
Tianjin University
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Hong Li
National Engineering Research Ceter of Distillation Technology
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Xin Gao
Tianjin university
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Abstract

As an attractive alternative technology for the separation of long chain olefin and paraffin, a novel silver-based deep eutectic solvent (Ag-DES) was prepared and utilized for 1-octene/n-octane separation. Comprehensive reactive extraction separation experiments were performed to highlight the Ag-DES concentration and operating temperature discriminations using compounds with different ratio of 1-octene/n-octane. The novel Ag-DES showed optimal separation performance regarding 1-octene/n-octane and possessed the highest levels separation selectivity in the range 3.75-16.74 with excellent circulation stability in our best knowledge. Furthermore, FT-Raman measurements and quantum chemistry calculation were conducted to elucidate the interaction mechanism of Ag-DES in the separation of 1-octene and n-octane, which revealed that both chemical complexation and strong physical attraction existed in the complex of Ag-DES with 1-octene rather than n-octane. This study lends important insight for the development of Ag-DES reactive extraction separation process for the energy-efficient long chain α-olefin purification from F-T synthesis products.
25 Oct 2020Submitted to AIChE Journal
27 Oct 2020Submission Checks Completed
27 Oct 2020Assigned to Editor
04 Nov 2020Reviewer(s) Assigned
12 Jan 2021Editorial Decision: Revise Major
26 Jan 20211st Revision Received
29 Jan 2021Submission Checks Completed
29 Jan 2021Assigned to Editor
01 Feb 2021Reviewer(s) Assigned
18 Feb 2021Editorial Decision: Accept
16 Mar 2021Published in AIChE Journal. 10.1002/aic.17252