Alcohol‐Treated Nickel‐Aluminium Catalyst for One‐Step Highly‐Selective Butane‐1,4‐Diol Synthesis from 2‐Butyne‐1,4‐Diol

Author:

Zhu Caixia1,He Yingluo1,Kushita Ryotaro1,Peng Xiaobo2,Ma Qingxiang3,Liu Guangbo4,Wu Jinhu4,Yang Guohui1,Tsubaki Noritatsu1ORCID

Affiliation:

1. Department of Applied Chemistry School of Engineering University of Toyama Gofuku 3190 Toyama 930-8555 Japan

2. National Engineering Research Center of Chemical Fertilizer Catalyst College of Chemical Engineering Fuzhou University Fuzhou Fujian 350002 P. R. China

3. State Key Laboratory of High-Efficiency Coal Utilization and Green Chemical Engineering School of Chemistry and Chemical Engineering Ningxia University Yinchuan Ningxia 750021 P. R. China

4. Key Laboratory of Biofuels Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao Shandong 266101 P. R. China

Abstract

AbstractThe development of low‐cost nickel‐based catalysts for direct and selective hydrogenation of 2‐butyne‐1,4‐diol (BYD) to butane‐1,4‐diol (BAD) under mild conditions is an important and attractive target both in fundamental research and industrialization but remains a formidable challenge. The primary industrial production method for BAD synthesis is a two‐step reaction route, which suffers from complicated catalysis conditions and high equipment costs. Herein, we develop a high‐performance catalyst via a facile alcohol‐treated strategy for highly selective BAD synthesis at moderate operation conditions. The as‐synthesized NA‐80E catalyst exhibits outstanding BAD selectivity of 98.82 % and BYD conversion of 100 % at 60 °C and 4 MPa, outperforming most reported results for BAD formation in a one‐step process and even being comparable to those obtained by the two‐step hydrogenation reaction route under much high temperatures and pressures. Crucially, we found that after facile alcohol (ethanol) treatment, an intriguing phenomenon of suppression of adjacent acid‐assisted hydrogenolysis via extra acidic Al species at the NiO‐Al2O3 interface is observed, contributing to the precise enhancement of BAD selectivity by inhibiting the production of butanol (BOL). This facile alcohol‐treated method along with the revealed mechanism of blocked hydrogenolysis opens vast possibilities for designing high‐performance and highly‐selective hydrogenation catalysts.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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