4.7 Article

Chemoselective decarboxylation of higher aliphatic esters to diesel-range alkanes over the NiCu/Al2O3 bifunctional catalyst under mild reaction conditions

期刊

RENEWABLE ENERGY
卷 180, 期 -, 页码 1-13

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2021.08.004

关键词

Selective decarboxylation; Bifunctional catalyst; Synergistic catalysis; Diesel-range alkanes

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A highly efficient NiCu/Al2O3 bifunctional catalyst has been developed for the production of diesel-range alkanes from higher aliphatic esters under mild reaction conditions. The catalyst showed excellent catalytic performance in model substrate, soybean oil, and waste cooking oil conversions, mainly due to the synergistic effect between the metal active sites and Lewis acid sites. The introduction of Cu species in the bimetallic catalyst greatly reduced the activation energy of the conversion reaction, leading to high decarboxylation performance under mild conditions.
An efficient and highly selective decarboxylation catalyst has been developed for the production of diesel-range alkanes from the conversion of higher aliphatic esters under mild reaction conditions. Using methyl stearate as a model substrate, the NiCu/Al2O3 bifunctional catalysts derived from layer double hydroxide (LDHs) precursors showed excellent catalytic performance with 100% conversion and 97.5% selectivity to heptadecane at 260 degrees C and 3.0 MPa H-2. On the other hand, the catalytic performance of NiCu/Al2O3 catalyst was also tested in the conversion of soybean and waste cooking oils under the mild conditions. The results showed that a high yields of diesel-range alkanes (>80 wt%) were obtained from the conversion of soybean oil and waste cooking oil, respectively. Detailed characterization (XRD, H-2-TPR, HRTEM, XPS, and NH3-TPD) indicates, after reduction at 500 degrees C in H-2 atmosphere, the NiCu alloy phase is the predominant phase and the Ni, Cu, Al species exhibited homogeneous distribution in the NiCu/Al2O3 catalyst. The remarkable decarboxylation performance mainly results from the synergistic effect between the metal active sites of NiCu alloy and Lewis acid sites of support Al2O3. The Lewis acid sites (Al3+) of support serve as active sites for the activation of carbonyl group of higher aliphatic esters, while H-2 dissociation and decarbonylation of intermediate fatty alde-hyde are achieved on the NiCu alloy sites. Compared with the monometallic Ni/Al2O3 catalyst (183.8 kJ/ mol), the introduction of Cu species in the bimetallic NiCu/Al2O3 catalyst greatly reduced the activation energy (138.1 kJ/mol) of fatty acid ester conversion via promoting the dispersion of Ni species, reducing the dissociation energy of hydrogen on Ni, and increasing the electron density of Ni, which results in high decarboxylation performance of NiCu/Al2O3 under mild reaction conditions. (c) 2021 Elsevier Ltd. All rights reserved.

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