Abstract

Waste cooking oil (WCO) hydrotreating to produce green diesel is good for both the environmental protection and energy recovery problems. The roles of catalyst support and reaction temperature on reactions during WCO hydrotreating process were evaluated over an unsupported and a commercial sulfided cobalt and molybdenum (CoMoS) catalyst supported by a mixture of Al2O3, TiO2, and SiO2. The presence of catalyst support helped to improve the dispersion and enlarge the surface area of CoMoS, and was found to be a key factor in reducing reaction temperature, in enhancing the hydrodeoxygenation (HDO) and hydrogenation capabilities, and in decreasing polymerization capability. The increase of reaction temperature strongly improved the deoxygenation, hydrogenation, and cracking reaction activities. Compared to the unsupported CoMoS, the supported one exhibited good deoxygenation and hydrogenation capabilities at 340 °C in WCO hydrotreating to produce diesel fraction; however, high temperature operation needs to be carefully controlled because it may cause overcracking and dehydrogenation.

Highlights

  • Renewable biofuels can reduce greenhouse gas emissions because of the carbon fixation that occurs during plant growth through the process of photosynthesis [1]

  • The Si/(Si+Al) ratio of catalyst support significantly affected the total acidic sites of catalyst, further changed the deoxygenation reaction rates and pathways [21]. Due to these conflicting results and the lack of studies to discuss non-deoxygenation reactions took place at the same time during waste cooking oil (WCO) hydrotreatment, it is necessary to investigate the roles of catalyst support on triglyceride hydrotreating

  • This present work investigated the roles of catalyst support on WCO hydrotreating process by three categories reactions: deoxygenation, hydrogenation/dehydrogenation, and cracking/polymerization by comparing an unsupported CoMoS

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Summary

Introduction

Renewable biofuels can reduce greenhouse gas emissions because of the carbon fixation that occurs during plant growth through the process of photosynthesis [1]. The Si/(Si+Al) ratio of catalyst support significantly affected the total acidic sites of catalyst, further changed the deoxygenation reaction rates and pathways [21] Due to these conflicting results and the lack of studies to discuss non-deoxygenation reactions took place at the same time during WCO hydrotreatment, it is necessary to investigate the roles of catalyst support on triglyceride hydrotreating. CoMoS catalysts are widely used in petroleum or its fraction hydrotreatment processes; they are more applied in industrial plant This present work investigated the roles of catalyst support on WCO hydrotreating process by three categories reactions: deoxygenation, hydrogenation/dehydrogenation, and cracking/polymerization by comparing an unsupported CoMoS catalyst and a supported (Al2 O3 -TiO2 -SiO2 ) CoMoS catalyst at different reaction temperatures. The main objectives were to explore the reaction routes, to identify the effects of support/temperature on product distributions and compositions, and to provide a basis for industrial production using the triglyceride hydrotreating process

Catalyst Morphology and Basic Properties
Regarding
Active Site Distribution
Reaction Route
Types of Oxygen
This suggests that HDO was the main main reaction thesupported supported
Catalyst Preparation and Evaluation
Catalyst Characterization
Product Analysis
Calculations
Conclusions
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