TY - JOUR
T1 - Solvent-mediated electrochemical acetylene semihydrogenation for continuous production of polymer-grade ethylene
AU - Wang, Xuxu
AU - Chen, Wenqian
AU - Lei, Xiaojia
AU - Wang, Xin
AU - Lei, Chao
AU - Xie, Qianqian
AU - Hu, Yongyou
AU - Zhou, Yi Ge
AU - Wang, Tiefeng
AU - Zhang, Jian
AU - Huang, Binbin
N1 - Publisher Copyright:
© 2026 Elsevier Inc.
PY - 2026
Y1 - 2026
N2 - The purification of crude ethylene is an energy-intensive process facing the challenges of high temperature, poor stability, and low ethylene selectivity. Here, we report a solvent-mediated electrochemical acetylene semihydrogenation approach that operates under mild conditions by exploiting differences in solvent absorption between acetylene and ethylene without solvent loss. This strategy significantly enhances the selective dissolution and diffusion of acetylene impurities to the cathode surface and drives their rapid hydrogenation to ethylene at the electron- and proton-rich liquid-solid interface. Over a 200-h continuous-flow stability test, the conversion of acetylene to ethylene remained at ∼100% with an ethylene selectivity of >99% and residual acetylene of <5 ppm under a crude ethylene stream. Theoretical, physical, and operando spectroscopic investigations revealed that solvent-mediated electrochemical acetylene semihydrogenation is thermodynamically favorable and follows a proton-coupled electron-transfer mechanism with water as the hydrogen source and that the solvent regulates catalytic activity and the hydrogenation mechanism.
AB - The purification of crude ethylene is an energy-intensive process facing the challenges of high temperature, poor stability, and low ethylene selectivity. Here, we report a solvent-mediated electrochemical acetylene semihydrogenation approach that operates under mild conditions by exploiting differences in solvent absorption between acetylene and ethylene without solvent loss. This strategy significantly enhances the selective dissolution and diffusion of acetylene impurities to the cathode surface and drives their rapid hydrogenation to ethylene at the electron- and proton-rich liquid-solid interface. Over a 200-h continuous-flow stability test, the conversion of acetylene to ethylene remained at ∼100% with an ethylene selectivity of >99% and residual acetylene of <5 ppm under a crude ethylene stream. Theoretical, physical, and operando spectroscopic investigations revealed that solvent-mediated electrochemical acetylene semihydrogenation is thermodynamically favorable and follows a proton-coupled electron-transfer mechanism with water as the hydrogen source and that the solvent regulates catalytic activity and the hydrogenation mechanism.
KW - carbon emission
KW - carbon neutrality technology
KW - electrochemical acetylene hydrogenation
KW - ethylene production
KW - ethylene purification
KW - liquid-phase hydrogenation
KW - polymer-grade ethylene
KW - proton-coupled electron transfer
KW - solvent absorption
KW - solvent-mediated hydrogenation
UR - https://www.scopus.com/pages/publications/105037751381
U2 - 10.1016/j.chempr.2026.103063
DO - 10.1016/j.chempr.2026.103063
M3 - 文章
AN - SCOPUS:105037751381
SN - 2451-9308
JO - Chem
JF - Chem
M1 - 103063
ER -