RESUMO
This article reports a safe, low-cost, and industrially applicable magnetite supported on activated carbon catalyst that can be magnetically retrieved from the solid and reused multiple times without the need of a regeneration step. The FeOx/C catalyst improved the bio-oil yield by 19.7 ± 0.96 % when compared to the uncatalysed reaction at 320 °C for the HTL of draff (brewer's spent grains). The use of homogeneous Na2CO3 base as a catalyst and co-catalyst, improved carbon extraction into the aqueous phase. The exceptional catalytic activity can be attributed to the Fe3O4 phase which can produce in-situ H2 that improves the biomass decomposition and oil property with an energy recovery of â¼84 %. The FeOx/C catalyst was separated using magnetic retrieval and maintained its catalytic activity even up to 5 reaction cycles showing potential as a cheap catalyst for HTL reactions and can be scaled-up for industrial applications.
Assuntos
Biocombustíveis , Óleos de Plantas , Temperatura , Biomassa , ÁguaRESUMO
NiMoS2 nanoparticles supported on carbon, synthesized by a microemulsion method were used as a nanocatalyst for hydrodeoxygenation (HDO) of a lignin model compound - guaiacol. Two types of carbon supports - mesoporous carbon (CMK-3) and activated carbon (AC) with a predominantly microporous structure, were studied to investigate the role of porosity and nature of the porous structure in catalyst activity. The activity of NiMoS2/AC resulted in the complete guaiacol conversion at 13 h of reaction time to produce phenol (31.5 mol%) and cyclohexane (35.7 mol%) as the two main products. Contrastingly, NiMoS2/CMK-3 needed a much lesser reaction time (6 h) to attain a similar conversion of guaiacol but gave different selectivities of phenol (25 mol%) and cyclohexane (55.5 mol%). Increased cyclohexane production with NiMoS2/CMK-3 implied better deoxygenation of MoS2 and enhanced hydrogenation capacity of Ni since phenol is a partially deoxygenated product of guaiacol while cyclohexane is a completely deoxygenated and hydrogenated product. The superior catalytic activity and deoxygenating behavior of NiMoS2/CMK-3 catalysts could be attributed to the organized mesoporosity of the CMK-3 support in relation to the improved active phase distribution and access to active sites that facilitate the conversion of the reaction's product. Recyclability study implied NiMoS2/CMK-3 was more stable without significant changes in the catalytic activity even after three reaction cycles.
RESUMO
A water-THF biphasic system containing N-methyl-2-pyrrolidone (NMP) was found to enable the efficient synthesis of 5-hydroxymethylfurfural (HMF) from a variety of sugars (simple to complex) using phosphated TiO2 as a catalyst. Fructose and glucose were selectively converted to HMF resulting in 98 % and 90 % yield, respectively, at 175 °C. Cellobiose and sucrose also gave rise to high HMF yields of 94 % and 98 %, respectively, at 180 °C. Other sugar variants such as starch (potato and rice) and cellulose were also investigated. The yields of HMF from starch (80-85 %) were high, whereas cellulose resulted in a modest yield of 33 %. Direct transformation of cellulose to HMF in significant yield (86 %) was assisted by mechanocatalytic depolymerization-ball milling of acid-impregnated cellulose. This effectively reduced cellulose crystallinity and particle size, forming soluble cello-oligomers; this is responsible for the enhanced substrate-catalytic sites contact and subsequent rate of HMF formation. During catalyst recyclability, P-TiO2 was observed to be reusable for four cycles without any loss in activity. We also investigated the conversion of the cello-oligomers to HMF in a continuous flow reactor. Good HMF yield (53 %) was achieved using a water-methyl isobutyl ketone+NMP biphasic system.