Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Mechanisms of catalytic cleavage of benzyl phenyl ether in aqueous and apolar phases

Journal Article · · Journal of Catalysis

Catalytic pathways for the cleavage of ether bonds in benzyl phenyl ether (BPE) in liquid phase using Ni- and zeolite-based catalysts are explored. In the absence of catalysts, the C-O bond is selectively cleaved in water by hydrolysis, forming phenol and benzyl alcohol as intermediates, followed by alkylation. The hydronium ions catalyzing the reactions are provided by the dissociation of water at 523 K. Upon addition of HZSM-5, rates of hydrolysis and alkylation are markedly increased in relation to proton concentrations. In the presence of Ni/SiO2, the selective hydrogenolysis dominates for cleaving the Caliphatic-O bond. Catalyzed by the dual-functional Ni/HZSM-5, hydrogenolysis occurs as the major route rather than hydrolysis (minor route). In apolar undecane, the non-catalytic thermal pyrolysis route dominates. Hydrogenolysis of BPE appears to be the major reaction pathway in undecane in the presence of Ni/SiO2 or Ni/HZSM-5, almost completely suppressing radical reactions. Density functional theory (DFT) calculations strongly support the proposed C-O bond cleavage mechanisms on BPE in aqueous and apolar phases. These calculations show that BPE is initially protonated and subsequently hydrolyzed in the aqueous phase. Finally, DFT calculations suggest that the radical reactions in non-polar solvents lead to primary benzyl and phenoxy radicals in undecane, which leads to heavier condensation products as long as metals are absent for providing dissociated hydrogen.

Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
1118103
Report Number(s):
PNNL-SA-97749; 47408; KC0302010
Journal Information:
Journal of Catalysis, Journal Name: Journal of Catalysis Journal Issue: C Vol. 311; ISSN 0021-9517
Publisher:
Elsevier
Country of Publication:
United States
Language:
English

Similar Records

Mechanisms of selective cleavage of C–O bonds in di-aryl ethers in aqueous phase
Journal Article · Tue Dec 31 23:00:00 EST 2013 · Journal of Catalysis · OSTI ID:1118104

Mechanocatalytic Hydrogenolysis of the Lignin Model Dimer Benzyl Phenyl Ether over Supported Palladium Catalysts
Journal Article · Mon Aug 05 00:00:00 EDT 2024 · ACS Sustainable Chemistry & Engineering · OSTI ID:2440574

Synergistic effects of Ni and acid sites for hydrogenation and C–O bond cleavage of substituted phenols
Journal Article · Sat Jan 31 23:00:00 EST 2015 · Green Chemistry · OSTI ID:1643788