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Flower-like nickel phosphide catalyst for petroleum resin hydrogenation with enhanced catalytic activity, hydrodesulfurization ability and stability.

Authors :
Wang, Rong
Sun, Hongming
Liang, Mengxin
Zhang, Hongwei
Cui, Qingyan
Wang, Tinghai
Yuan, Pei
Source :
Chemical Engineering Science. Dec2022, Vol. 264, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

[Display omitted] • The flower-like nickel phosphide catalysts were prepared by a hydrotalcite strategy. • Ni 2 P/Al 2 O 3 catalyst showed excellent catalytic activity and desulfurization ability. • The outstanding performance ascribed to the rich active Niδ+ species. • The enhanced stability was due to strong interaction between active sites and support. The catalytic hydrogenation of petroleum resin (PR) to high value-added hydrogenated PR (HPR) represents a forward-looking technology for upgrading the pyrolysis petroleum by-product. Herein, flower-like and pure-phase supported nickel phosphide catalysts were controllably fabricated through a hydrotalcite strategy with red phosphorous as the P source. The PR hydrogenation activity of the catalysts followed the order of Ni 2 P/Al 2 O 3 > NiP 2 /Al 2 O 3 > Ni/Al 2 O 3 > imp-Ni 2 P/Al 2 O 3 catalysts (prepared by the impregnation method). Such enhanced performance of Ni 2 P/Al 2 O 3 could be ascribed to small nickel phosphide particle size and rich active Niδ+ species. Notably, the sulfur contents of PR were effectively reduced from 55.4 (C 5 PR) and 72.3 ppm (C 9 PR) to 3.8 and 7.9 ppm after hydrogenation by Ni 2 P/Al 2 O 3. Meanwhile, Ni 2 P/Al 2 O 3 also exhibited good stability with the hydrogenation degree of HC 5 PR maintaining at 94.39 % after 100 h. Our work provides a promising nickel phosphide catalyst with outstanding hydrogenation activity, hydrodesulfurization ability, and stability toward PR hydrogenation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00092509
Volume :
264
Database :
Academic Search Index
Journal :
Chemical Engineering Science
Publication Type :
Academic Journal
Accession number :
159994530
Full Text :
https://doi.org/10.1016/j.ces.2022.118180