4.6 Article

Hydrodeoxygenation of non-edible bio-lipids to renewable hydrocarbons over mesoporous SiO2-TiO2 supported NiMo bimetallic catalyst

Journal

APPLIED CATALYSIS A-GENERAL
Volume 633, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcata.2021.118475

Keywords

Bio-lipids; Hydrodeoxygenation; Ni-Mo/SiO2-TiO2 catalysts; eta(2)(CO)-aldehyde configuration; Bronsted acidic sites

Funding

  1. National Natural Science Foundation of China [21878255, 21676629]
  2. Scientific Research Fund of Hunan Provincial Education Department [21A0084]
  3. Hunan Provincial Innovation Foundation for Postgraduate [CX2018B043]
  4. Innovation Platform Open Founds of Hunan Provincial [16K086]
  5. Key R & D Project of Hunan Science and Technology Department [2017GK2020]
  6. Hunan Provincial Natural Science Foundation of China [2018JJ2385]

Ask authors/readers for more resources

A mesoporous Ni-Mo/SiO2-TiO2 catalyst was prepared and used for fatty acid hydrodeoxygenation with high yield and selectivity. Experimental results showed that Mo-addition and adjusting Ti/Si molar ratio significantly influenced HDO selectivity.
Ni-catalysts are promising candidate for fatty acid hydrodeoxygenation (HDO), but are limited by their quite poor HDO selectivity. Herein, a mesoporous Ni-Mo/SiO2-TiO2 catalyst was prepared by precipitation and impregnation method and used for methyl laurate HDO, yielding 96.3% n-dodecane yield at full methyl laurate conversion. Non-edible bio-lipids such as jatropha oil and waste cooking oil also converted to n-C14+16+18 hy-drocarbons with yields of 94.3% and 92.4%, respectively. Besides, Ni-Mo/SiO2TiO2 shows strong chemo-selectivity towards the HDO of ester groups. Experimental results showed that Mo-addition and Ti/Si molar ratio strongly influenced HDO selectivity. Oxygen vacancies formed on partial reduced TiO2 surface securely bond Ni NPs and activate C=O/C-O bonds, improving Ni NPs dispersion and promoting R-COOCH3 R-CHO reduction. Additional, Mo-addition switches reactant adsorption configuration from eta(1)(C)-acyl to eta(2)(C,O)-aldehyde, pro-moting the formation of R-CH2OH intermediate. Moreover, abundant Bronsted acidic sites (Mo4+-OH, Mo6+-OH, hydroxy groups) facilitate the HDO of R-CH2OH to R-CH3.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available