The catalytic hydrogenolysis of lignin has been reported as an effective approach for lignin depolymerization owing to its high efficiency for aromatic monomer production. In this study, a series of copper monometallic catalysts over an MIL-101(Cr) support were synthesized and used for the catalytic hydrogenolysis of alkali lignin using supercritical ethanol. First, the optimal copper catalyst for lignin hydrogenolysis was selected. Subsequently, the reaction conditions for catalytic hydrogenolysis were systematically optimized to maximize the total monomer yield. The optimal conditions were determined to be 6 h of reaction time, 20 min of sonication pretreatment, 50% catalyst loading, and 5% lignin loading. Under these conditions, an aromatic monomer yield of 38.5% was obtained; this depolymerized lignin stream, which is mainly composed of G-type monomers, can serve as a promising aromatic feedstock and carbon source for further microbial upgrading and bioconversion to produce various value-added products.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.biortech.2021.125941 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
University of California, Riverside, Chemistry, 501 Big Springs Rd, 92521, Riverside, UNITED STATES OF AMERICA.
Sulfated zirconium oxide (SZO) catalyzes the hydrogenolysis of isotactic polypropylene (iPP, Mn = 13.3 kDa, Đ = 2.4,
Int J Biol Macromol
December 2024
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China. Electronic address:
The conversion of abundant lignin was of great significance for the utilization of biomass resources. In this study, lignin sulfonate (LS) was selected as a carbon-based support, which was successfully introduced into the NiCo-MOF structure. A series of lignin and MOF hybrid catalysts (NiCo-MOF-LS) with varying metal ratios of Ni and Co were synthesized via the hydrothermal method.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China. Electronic address:
Lignin represents a significant source of aromatic hydrocarbons in the natural world. The production of high-value chemicals from lignin has the great potential to effectively address the issue of fossil energy scarcity. In this study, complex sulfides of nickel‑cobalt bimetallic catalysts were prepared via hydrothermal synthesis and subsequently employed in the catalytic hydrogenolysis of CO bonds present in lignin.
View Article and Find Full Text PDFACS Nano
December 2024
School of Environment and Energy, State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control, South China University of Technology, Guangzhou 510006, China.
Bimetallic Pt-based catalysts, for example, PtZn and PtSn catalysts, have gained significant attention for addressing the poor stability and low selectivity of pristine Pt catalysts over propane dehydrogenation (PDH). However, the structures of the active sites and the corresponding catalytic mechanism of PDH are still elusive. Here, we demonstrate a spatially confined Pt-ZnO@RUB-15 catalyst (where "" is the mole ratio of Zn/Pt and RUB-15 is a layered silica), which exhibited high catalytic activity, ultrahigh selectivity (>99%), and resistance to coking at 550 °C for PDH.
View Article and Find Full Text PDFJ Phys Chem B
December 2024
College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065, P.R. China.
The hydrogenolysis of lignin model compounds (MCs) into high-value chemicals has received increasing attention, but their catalytic reaction mechanisms are not yet very clear. Here, we report the reaction mechanisms of the hydrogenolysis of MC into 4-acetylanisole (AAL) and guaiacol (GAL) catalyzed by LRuCl (L = 4'-(4-methoxyphenyl)-2,2':6',2″-terpyridine) with MC, H, and 1-phenylethan-1-ol (PEO) as the H-sources in aqueous solution with the Bro̷nsted base (NaOH), at the M06/def2-TZVP, 6-311++G (d,p) theoretical level, namely, RS-Self, RS-H, and RS-PEO, respectively. After dissociation in NaOH aqueous solution, the LRuCl compound can form a stable complex LRh (OH) as the initial catalytically active species.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!