TY - JOUR
T1 - MOF-199 and Ni-BTC
T2 - Synthesis, Physicochemical Properties, and Catalytic Activity in Oxidation of 5-Hydroxymethylfurfural
AU - Herlina, Idra
AU - Krisnandi, Yuni Krisyuningsih
AU - Ridwan, Muhammad
N1 - Publisher Copyright:
Copyright © 2023 by Authors, Published by BCREC Group.
PY - 2023
Y1 - 2023
N2 - Platform chemical 2,5-furandicarboxylic acid (FDCA) has potential applications to replace petroleum-based chemicals. Metal Organic Framework (MOF) can be used as a catalyst to oxidize 5-hydroxymethylfurfural (HMF), producing FDCA. MOF-199 and Ni-BTC were synthesized using solvothermal method with trimesic acid (benzene 1,3,5-tricarboxylic acid/H3BTC) as a linker and Cu or Ni as a metal nod. The physical and chemical properties of catalysts were discovered through characterization using X-ray Diffraction (XRD), Fourier Transform Infra Red (FT-IR), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy - Energy Dispersive X-ray (SEM-EDX), and Ammonia Temperature-programmed Desorption (NH3-TPD). FDCA and its intermediate compounds were produced by converting HMF to FDCA in a small glass batch reactor. The yields of products were then determined by High-Performance Liquid Chromatography (HPLC). HPLC results indicated that there was no DFF (2,5-diformylfuran) signal, indicating that FDCA was formed by FFCA (5-formylfuroic acid) and HMFCA (5-hydroxymethylfuroic acid) formation reaction pathway. The maximum conversion (71%) was obtained using Ni-BTC as a catalyst at 130 °C for 5 h, with FDCA yield of 61.8%.
AB - Platform chemical 2,5-furandicarboxylic acid (FDCA) has potential applications to replace petroleum-based chemicals. Metal Organic Framework (MOF) can be used as a catalyst to oxidize 5-hydroxymethylfurfural (HMF), producing FDCA. MOF-199 and Ni-BTC were synthesized using solvothermal method with trimesic acid (benzene 1,3,5-tricarboxylic acid/H3BTC) as a linker and Cu or Ni as a metal nod. The physical and chemical properties of catalysts were discovered through characterization using X-ray Diffraction (XRD), Fourier Transform Infra Red (FT-IR), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy - Energy Dispersive X-ray (SEM-EDX), and Ammonia Temperature-programmed Desorption (NH3-TPD). FDCA and its intermediate compounds were produced by converting HMF to FDCA in a small glass batch reactor. The yields of products were then determined by High-Performance Liquid Chromatography (HPLC). HPLC results indicated that there was no DFF (2,5-diformylfuran) signal, indicating that FDCA was formed by FFCA (5-formylfuroic acid) and HMFCA (5-hydroxymethylfuroic acid) formation reaction pathway. The maximum conversion (71%) was obtained using Ni-BTC as a catalyst at 130 °C for 5 h, with FDCA yield of 61.8%.
KW - 2,5-furandicarboxylic acid
KW - 5-hydroxymethylfurfural
KW - MOF-199
KW - Ni-BTC
UR - http://www.scopus.com/inward/record.url?scp=85181172952&partnerID=8YFLogxK
U2 - 10.9767/bcrec.20060
DO - 10.9767/bcrec.20060
M3 - Article
AN - SCOPUS:85181172952
SN - 1978-2993
VL - 18
SP - 724
EP - 735
JO - Bulletin of Chemical Reaction Engineering and Catalysis
JF - Bulletin of Chemical Reaction Engineering and Catalysis
IS - 4
ER -