Efficient Conversion of Biomass‐Derived Furfural to Tetrahydrofurfuryl Alcohol over Co3O4−C Nanocomposite Catalyst at Mild Conditions

Author:

Van Nguyen Chi12ORCID,Le Giau M.34,Nguyen Tung T.34,Van Tran Thuan5,Vu Thanh Dien To67,Nguyen Phuong‐Tung12,Ngoc Tran Quyen12,Phan Nam T. S.34

Affiliation:

1. Graduate University of Science and Technology Vietnam Academy of Science and Technology 18 Hoang Quoc Viet, Cau Giay District 122300 Ha Noi Vietnam

2. Institute of Applied Materials Science Vietnam Academy of Science and Technology 1D Thanh Loc 29 Street, Thanh Loc, District 12 122300 Ho Chi Minh City Vietnam

3. Department of Chemical Engineering Ho Chi Minh City University of Technology (HCMUT) 268 Ly Thuong Kiet, District 10 72560 Ho Chi Minh City Vietnam

4. Vietnam National University Ho Chi Minh City Linh Trung Ward, Thu Duc District 72560 Ho Chi Minh City Vietnam

5. Institute of Applied Technology and Sustainable Development Nguyen Tat Thanh University 300A Nguyen Tat Thanh, District 4 Ho Chi Minh City 755414 Vietnam

6. Institute for Advanced Material Technology Van Lang University 69/68 Dang Thuy Tram 72311 Ho Chi Minh City Vietnam

7. Faculty of Applied Technology School of Technology, Van Lang University 72311 Ho Chi Minh City Vietnam

Abstract

AbstractDue to the depletion of fossil fuel resources, catalytic conversion of biomass into liquid fuels and valuable compounds has become an attractive field of research. Tetrahydrofurfuryl alcohol (THFAL) is an important platform molecule in both industrial and pharmacological fields, and catalytic hydrogenation of furfural (FA) to THFAL is a sustainable process. However, an active and stable catalyst for the direct hydrogenation of FA to THFAL under milder conditions is still a challenge. Accordingly, herein, we investigated a high‐valence metal catalyst (Co3O4−C) for the hydrogenation of FA to THFAL using sodium borohydride (NaBH4) as the H source. Under optimal reaction conditions (that is, 0.05 g Co3O4−C‐700 in an aqueous solution, 5 mmol NaBH4, 60 °C, and 3 h), 88.5 % THFAL was produced over Co3O4−C‐700. The kinetic study revealed that furfuryl alcohol was generated as an intermediate during the hydrogenation of FA. Additionally, the reaction followed pseudo‐first order kinetics, and the reaction rate constant (k) values were .80, 3.41, 3.45, and 5.55 h−1 at 30, 40, 45, 50, and 60 °C, respectively. From the slopes of the Arrhenius plot, the activation energy was determined to be 22.02 kJ mol−1, indicating high activity of the catalyst for the reaction. Moreover, Co3+ and smaller sizes of Co3O4 nanoparticles contributed to the activity of Co3O4−C‐700. We believe that the metal oxide catalyst developed herein can be used for various biomass conversions.

Funder

Graduate University of Science and Technology, Vietnam Academy of Science and Technology

Vietnam Academy of Science and Technology

Publisher

Wiley

Subject

General Chemistry

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