Fast pyrolysis of lignocellulosic biomass produces a renewable liquid fuel called pyrolysis oil that is the cheapest liquid fuel produced from biomass today. Here we show that pyrolysis oils can be converted into industrial commodity chemical feedstocks using an integrated catalytic approach that combines hydroprocessing with zeolite catalysis. The hydroprocessing increases the intrinsic hydrogen content of the pyrolysis oil, producing polyols and alcohols. The zeolite catalyst then converts these hydrogenated products into light olefins and aromatic hydrocarbons in a yield as much as three times higher than that produced with the pure pyrolysis oil. The yield of aromatic hydrocarbons and light olefins from the biomass conversion over zeolite is proportional to the intrinsic amount of hydrogen added to the biomass feedstock during hydroprocessing. The total product yield can be adjusted depending on market values of the chemical feedstocks and the relative prices of the hydrogen and biomass.
Catalytic conversion of ten biomass-derived feedstocks, i.e. glucose, sorbitol, glycerol, tetrahydrofuran, methanol and different hydrogenated bio-oil fractions, with different hydrogen to carbon effective (H/C eff ) ratios was conducted in a gas-phase flow fixed-bed reactor with a ZSM-5 catalyst. The aromatic + olefin yield increases and the coke yield decreases with increasing H/C eff ratio of the feed. There is an inflection point at a H/C eff ratio ¼ 1.2, where the aromatic + olefin yield does not increase as rapidly as it does prior to this point. The ratio of olefins to aromatics also increases with increasing H/ C eff ratio. CO and CO 2 yields go through a maximum with increasing H/C eff ratio. The deactivation rate of the catalyst decreases significantly with increasing H/C eff ratio. Coke was formed from both homogeneous and heterogeneous reactions. Thermogravimetric analysis (TGA) for the ten feedstocks showed that the formation of coke from homogeneous reactions decreases with increasing H/C eff ratio. Feedstocks with a H/C eff ratio less than 0.15 produce large amounts of undesired coke (more than 12 wt %) from homogeneous decomposition reactions. This paper shows that the conversion of biomassderived feedstocks into aromatics and olefins using zeolite catalysts can be explained by the H/C eff ratio of the feed.
Chemical-looping combustion of biomass was carried out in a 10 kW th reactor with iron oxide as an oxygen carrier. A total 30 h of test was achieved with the same batch of iron oxide oxygen carrier. The effect of the fuel reactor temperature on gas composition of the fuel reactor and the air reactor, the proportion of biomass carbon reacting in the fuel reactor, and the conversion of biomass carbon to CO 2 in the fuel reactor was experimentally investigated. The results showed that the CO production from biomass gasification with CO 2 was more temperature dependent than the CO oxidation with iron oxide in the fuel reactor, and an increase in the fuel reactor temperature produced a higher increase for the CO production from biomass gasification than for the oxidation of CO by iron oxide. Although the conversion of biomass carbon to CO 2 in the fuel reactor decreased with the increase of the fuel reactor temperature, there was a substantial increase in the proportion of biomass carbon reacting in the fuel reactor. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were utilized to characterize fresh and reacted oxygen carrier particles. The results showed that the transformation of Fe 2 O 3 to Fe 3 O 4 is the favored step in the process of iron oxide reduction with biomass syngas. The low reactivity of reacted oxygen carrier was mainly ascribed to the sintering grains on the particle surface. To restrain the surface sintering of oxygen carrier particles, an intensive oxidization of reduced oxygen carrier with air in the air reactor should be avoided in the process of oxygen carrier regeneration, and air staging should be adopted for the oxidization of reduced oxygen carrier with air in the air reactor.
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