Bio-oil
is a mixture of organics produced from pyrolysis of biomass.
The organics in bio-oil serve as the feedstock for the production
of hydrogen, chemicals, biofuels, and carbon materials. In many processes
for conversion of bio-oil, heating is required. The thermal treatment
of bio-oil induces the polymerization/cracking of the organics in
bio-oil, producing coke. Coke could lower the carbon conversion efficiency
of bio-oil, clog the reactor chamber, and deactivate the catalyst,
imposing the main challenge for the utilization of bio-oil involving
the heating of bio-oil. This review investigates the coking issues
in the processes for bio-oil upgrading including esterification, hydrotreatment,
catalytic pyrolysis, pyrolysis, steam reforming, and the process for
the conversion of bio-oil to carbon materials. The properties of coke
formed from thermal treatment of bio-oil, the mechanism for coking
of bio-oil, and the methods developed for tackling the coking of bio-oil
are the focus.
Selectively hydrogenating
the carbonyl of furfural and opening
of the furan ring is challenging but crucial for efficient conversion
of furfural to pentanediols, the valuable chemicals. In this study,
CuMgAl catalysts with highly dispersed Cu particles and tunable basic
sites were synthesized with layered double hydroxides as precursors
for hydrogenation of furfural to furfuryl alcohol (FA) and the subsequent
hydrogenolysis of FA to 1,2-pentanediol and 1,5-pentanediol. The presence
of varied content of Mg in the catalyst promoted dispersion of copper
oxide and exposure of metallic copper species, weakened interaction
between copper oxides and the carrier, suppressed sintering of metallic
copper species, and increased abundance of the basic sites, promoting
the catalytic activity/selectivity/stability. Strong chemical adsorption
of the furan ring in FA on basic sites of the catalyst suppressed
hydrogenation of the furan ring and facilitated opening of the furan
ring in FA, the rate-determining step for formation of the diols.
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