Hydrotalcite-Based Bimetallic PdNi Catalysts with High Sulfur Tolerance for the Hydrogenation of Dicyclopentadiene Resin

被引:5
作者
Bai, Zongxuan [1 ,2 ]
Chen, Xiao [1 ]
Liang, Changhai [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Lab Adv Mat & Catalyt Engn, Dalian 116024, Peoples R China
[2] Bohai Univ, Coll Chem & Mat Engn, Jinzhou 121013, Peoples R China
基金
中国国家自然科学基金;
关键词
LAYERED DOUBLE HYDROXIDES; SELECTIVE HYDROGENATION; PETROLEUM RESINS; EFFICIENT; ALLOY; RESISTANCE; PERFORMANCE; REACTIVITY; PALLADIUM; MONOMER;
D O I
10.1021/acs.iecr.2c04663
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The catalytic hydrogenation of unsaturated bonds in petroleum resin is a promising way to enhance the properties of petroleum resin in terms of weather resistance, stability, and compatibility. However, the presence of sulfur compounds in petroleum resin poses a high challenge to hydrogenation catalysts. Herein, based on the cation-tunability of hydrotalcite-like compounds, a series of PdNi bimetallic catalysts are prepared by calcination-reduction of their hydrotalcite-like precursors and applied in the hydrogenation of dicyclopentadiene (DCPD) petroleum resin. By tuning the molar ratios of Pd/Ni and optimizing the reaction conditions, the optimal Pd1Ni1-MgAlO- HT catalyst can obtain the hydrogenated DCPD petroleum resin with saturation up to 91.5% at 255 degrees C, 10 MPa H2 pressure, and 3 h reaction time with the presence of 50 ppm sulfur compound. As compared with the monometallic catalyst, the PdNi bimetallic catalyst presents higher sulfur tolerance in the hydrogenation of DCPD petroleum resin. Combined with the analysis results of XRD, XPS, TEM, and H2-TPR, the enhanced catalytic performance of the Pd1Ni1-MgAlO-HT catalyst can be attributed to the small particle size, high dispersion of metal particles, and the synergy effect between Pd and Ni species. This work will guide to design a highly efficient sulfur tolerance catalyst derived from the hydrotalcite-like precursor for the hydrogenation of polymers.
引用
收藏
页码:6069 / 6080
页数:12
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