TY - JOUR
T1 - Investigation on fluorinated alumina catalysts prepared by the fluorination of γ-Al2O3 with CHF3 for the isomerization of E-1-chloro-3,3,3-trifluoropropene
AU - Feng, Shiwei
AU - Zhang, Chengping
AU - Quan, Hengdao
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/2/1
Y1 - 2023/2/1
N2 - As an environmentally friendly cleaning agent, Z-1-chloro-3,3,3-trifluoropropene (HCFO-1233zd(Z)) can realize industrial production by the isomerization of HCFO-1233zd(E). Herein, various isomerization catalysts with different structures, compositions and acid properties were prepared through the fluorination of γ-Al2O3 with CHF3 by controlling the activation conditions. For the first time, the catalysts for HCFO-1233zd(E) isomerization were systematically studied by XRD, N2 physisorption, XPS, SEM, MAS NMR spectroscopy, NH3-TPD and py-IR. The active site of this reaction was revealed and the catalyst deactivation mechanism was proposed. It turned out that HCFO-1233zd(E) isomerization prefers to occur at Lewis acid sites with moderate density and strength. The amorphous particles composed of γ-Al2O3, Al2O3(F) and α-AlF3 (R3¯c) at 450 °C exhibit highly catalytic activity for HCFO-1233zd(E) isomerization. After 100 h evaluation, it was found that residual γ-Al2O3 can be fluorinated by HCFO-1233zd(E) to form needle-like structures which could induce the amorphous Al2O3(F) particles to reorganize and give cubic structures, where the Lewis acid properties were enhanced, leading to catalyst deactivation.
AB - As an environmentally friendly cleaning agent, Z-1-chloro-3,3,3-trifluoropropene (HCFO-1233zd(Z)) can realize industrial production by the isomerization of HCFO-1233zd(E). Herein, various isomerization catalysts with different structures, compositions and acid properties were prepared through the fluorination of γ-Al2O3 with CHF3 by controlling the activation conditions. For the first time, the catalysts for HCFO-1233zd(E) isomerization were systematically studied by XRD, N2 physisorption, XPS, SEM, MAS NMR spectroscopy, NH3-TPD and py-IR. The active site of this reaction was revealed and the catalyst deactivation mechanism was proposed. It turned out that HCFO-1233zd(E) isomerization prefers to occur at Lewis acid sites with moderate density and strength. The amorphous particles composed of γ-Al2O3, Al2O3(F) and α-AlF3 (R3¯c) at 450 °C exhibit highly catalytic activity for HCFO-1233zd(E) isomerization. After 100 h evaluation, it was found that residual γ-Al2O3 can be fluorinated by HCFO-1233zd(E) to form needle-like structures which could induce the amorphous Al2O3(F) particles to reorganize and give cubic structures, where the Lewis acid properties were enhanced, leading to catalyst deactivation.
KW - Acid strength
KW - E-1-chloro-3,3,3-fluoropropene
KW - Fluorinated alumina
KW - Lewis acid sites
KW - Z-1-chloro-3,3,3-fluoropropene
UR - http://www.scopus.com/inward/record.url?scp=85146013816&partnerID=8YFLogxK
U2 - 10.1016/j.mcat.2023.112917
DO - 10.1016/j.mcat.2023.112917
M3 - Article
AN - SCOPUS:85146013816
SN - 2468-8231
VL - 536
JO - Molecular Catalysis
JF - Molecular Catalysis
M1 - 112917
ER -