29 research outputs found
From Biomass to Sugar Alcohols: Purification of Wheat Bran Hydrolysates Using Boronic Acid Carriers Followed by Hydrogenation of Sugars over Ru/H-ZSM-5
Wheat bran is a lignocellulosic waste of milling industry. It contains hemicelluloses, which can be valorized into arabitol and xylitol via a few-step approach. It begins with extraction and hydrolysis of hemicelluloses to produce a solution of xylose and arabinose, along with proteins and inorganic salts. This work focuses on the purification of sugars of this hydrolysate and the subsequent catalytic production of sugar alcohols. A purification process based on the recovery of sugars by anionic extraction with a boronic acid, followed by back-extraction and a further refining step with ion exchange resins is described. After this process, a high purity sugars solution (âŒ90%) free of inorganic elements and proteins was obtained. The feasibility of the process was also highlighted by a successful recycling of the organic phase containing the boronic acid. The hydrogenation of purified sugars was then performed over Ru/H-ZSM-5. A high yield into pentitols of âŒ70% with 100% selectivity was achieved. Importantly, the catalytic hydrogenation of sugars in the hydrolysate
prior to purification did not occur. We determined that proteins caused the deactivation of the catalyst, and consequently, the
inhibition of the production of sugar alcohols.Ministerio de EconomĂa, Industria y Competitividad - Fondo Europeo de Desarrollo Regional (project CTQ2015-64892-R
Porous Tin-Organic Frameworks as Selective Epimerization Catalysts in Aqueous Solutions
Epimerization of sugars is a carbon-efficient route not only to produce rare carbohydrates but also to extend the product scope for chemical production in future biorefineries. Industrially available catalysts for epimerization are limited mainly to soluble Mo(VI) species as well as substrate-specific epimerases. Here we report highly active and selective tin-organic frameworks (Sn-OF) as solid catalysts for the epimerization of aldoses at the C-2 position, such as the conversion of glucose to mannose. The reaction proceeds via a carbon skeleton rearrangement, that is, through breaking of a C-2/C-3 carbon bond and formation of a C-1/C-3 bond. Partially hydrolyzed PhâSn-OH sites were found to be the catalytically active centers. Our results suggest that the high catalytic activity of Sn-OFs for the epimerization is determined by (1) Lewis acidity of tin; (2) free Sn-OH groups; and (3) the high hydrophobicity of organic linkers applied in the aqueous solutions
Recommended from our members
Solvent effects on catalytic activity and selectivity in amine-catalyzed D-fructose isomerization
Rational catalyst design and optimal solvent selection are key to advancing biorefining. Here, we explored the organocatalytic isomerization of D-fructose to a valuable rare monosaccharide, D-allulose, as a function of solvent. The isomerization of D-fructose to D-allulose competes with its isomerization to D-glucose and sugar degradation. In both water and DMF, the catalytic activity of amines towards D-fructose is correlated with their basicity. Solvents impact the selectivity significantly by altering the tautomeric distribution of D-fructose. Our results suggest that the furanose tautomer of D-fructose is isomerized to D-allulose, and the fractional abundance of this tautomer increases as follows: water < MeOH < DMF â DMSO. Reaction rates are also higher in aprotic than in protic solvents. The best D-allulose yield, 14 %, was obtained in DMF with 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as the catalyst. The reaction kinetics and mechanism were explored using operando NMR spectroscopy
Alternative Monomers Based on Lignocellulose and Their Use for Polymer Production
Polymeric materials play a key role in modern industry. Owing to outstanding and very versatile properties of polymers, they have rather quickly occupied the great niche of commodities. World plastic production is continuously growing from 1.7 Mton/year in 1950 to 288 Mton/year in 2012. Fossil sources are still required for production of the major part of polymers, as only 5% of chemicals are currently produced from renewable feedstocks. Nevertheless, the application of natural chemicals as feedstocks for the manufacture of polymers is steadily increasing. Different motivations induce such a high interest toward new biobased materials. First of all, the global depletion of petroleum resources and their uneven spread over the world stimulate the rational use of biomass as a renewable and ubiquitous resource. Additionally, overwhelming of dumps with nondegradable plastics causes serious ecological problems, stimulating the developments toward new biodegradable materials. Here we have to point at the distinction between the terms âbiobasedâ and âbiodegradableâ. Biobased products are manufactured from renewable sources, but several examples of biobased and nonbiodegradable products, e.g., biopolyethylene, biopolyamide 11, exist. It should be noted that each new material has to be tested for biodegradability before it can be claimed to be so. For example, linear polymers produced from itaconic acid are biodegradable, but cross-linking of the polymer chains slows down the biodegradatio