Direct valorization of cellulose and glucose to glycolic acid through green catalytic process

The current work reports the catalytic conversion of α-cellulose to glycolic acid using molecular oxygen as an oxidant. A series of copper and cobalt molybdophosphoric acid catalysts (Cu-H3PMo12O40 and Co-H3PMo12O40) were synthesized via impregnation and ion-exchange techniques. Then the synthesized...

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Bibliographic Details
Main Authors: Madduluri, Venkata Rao, Lim, Mei Ying, Anisah Sajidah, Haji Saud, Maniam, Gaanty Pragas, Mohd Hasbi, Ab Rahim
Format: Article
Language:English
English
Published: Springer 2024
Subjects:
Online Access:http://umpir.ump.edu.my/id/eprint/40418/1/Direct%20valorization%20of%20cellulose%20and%20glucose%20to%20glycolic.pdf
http://umpir.ump.edu.my/id/eprint/40418/2/Direct%20valorization%20of%20cellulose%20and%20glucose%20to%20glycolic%20acid%20through%20green%20catalytic%20process_ABS.pdf
http://umpir.ump.edu.my/id/eprint/40418/
https://doi.org/10.1007/s10562-023-04360-9
https://doi.org/10.1007/s10562-023-04360-9
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Institution: Universiti Malaysia Pahang Al-Sultan Abdullah
Language: English
English
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Summary:The current work reports the catalytic conversion of α-cellulose to glycolic acid using molecular oxygen as an oxidant. A series of copper and cobalt molybdophosphoric acid catalysts (Cu-H3PMo12O40 and Co-H3PMo12O40) were synthesized via impregnation and ion-exchange techniques. Then the synthesized catalysts are thoroughly tested for effective conversion of α-cellulose and glucose into glycolic acid and value-added chemicals. The physicochemical characterization of as prepared catalysts was carried out using X-ray diffraction (XRD) and a scanning electron microscope-energy dispersive spectrometer (SEM–EDS). Fourier-transform infrared spectroscopy (FT-IR), N2-Physisorption and the Hammett test, on the other hand, were used to determine the quantitative relationship between catalyst structure and catalyst activity. Under mild reaction conditions, glycolic acid was discovered to be the primary product with 99.8% selectivity and 99% yield over a Cu-impregnated H3PMo12O40 catalyst. It was also revealed that the catalytic activity was directly related to the catalyst surface area, degree of crystallization, and surface acidic strength. Moreover, synergic interactions of active metals with support materials, Bronsted and Lewis acid properties possessed by catalysts are major determinants of better catalytic activity. Graphic Abstract: (Figure presented.).