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Development of cross-linked, soft polymeric materials from biomass has been a focus of research. The aqueous phase of biomass pyrolysis oil (bio-oil) has been used as a precursor for monomer synthe...

The sorption/desorption of gallic acid, a simple phenolic compound, was studied experimentally in a batch system. The motivation for this project was to provide insight into the recovery of phenolic compounds from switchgrass. Recovery of phenolic compounds could enhance the sustainability and economics of biorefining facilities. The sorption/desorption of gallic acid was shown to be qualitatively similar to that of phenolics extracted from switchgrass; so more extensive studies were made using gallic acid as a surrogate for the complex mixtures of phenolic compounds leached from switchgrass. The kinetics indicate that an approximation of equilibrium was reached within 48 h. Activated carbon was demonstrated to sorb gallic acid and phenolics from water and aqueous switchgrass leachate. The loading capacity of activated carbon for the gallic acid–water-activated carbon system increased with temperature for 20 to 60 °C. Ethanol was shown to be a preferable elution agent for desorbing gallic acid from activa...

A two-step thermochemical process combining a thermal desorption at 250–300 °C and a pyrolysis at 500 °C of used creosote-treated wooden railroad ties was carried out to recover preservative and produce a high quality bio-oil and biochar. Under optimal temperature between 280 and 300 °C, high preservative removal efficiency (70–74%) was achieved with a high proportion of polycyclic aromatic hydrocarbons (PAHs, 80–82%) and a large portion of the original wood mass (67–70%) was retained. This thermally treated biomass had higher heating value (HHV; 19.9–20 MJ/kg) than the starting material. The physical properties of the preservative, such as viscosity and density, and its toxic threshold against a common decay basidiomycete fungus were similar to those of commercially available P2-creosote. Pyrolysis of the thermally treated ties produced bio-oils with lower water content and total acid numbers, and a higher amount of lignin-derived compounds than that of untreated ties. Biochars derived from the thermally...

Reforming whole lignocellulosic biomass into value-added materials has yet to be achieved mainly due to the infusible nature of biomass and its recalcitrance to dissolve in common organic solvents. Recently, the solubility of biomass in ionic liquids (ILs) has been explored to develop all-lignocellulosic materials; however, efficient dissolution and therefore production of value-added materials with desired mechanical properties remain a challenge. This article presents an approach to producing high-performance lignocellulosic films from hybrid poplar wood. An autohydrolysis step that removes ≤50% of the hemicellulose fraction is performed to enhance biomass solvation in 1-ethyl-3-methyl imidazolium acetate ([C2mim][OAc]). The resulting biomass–IL solution is then cast into free-standing films using different coagulating solvents, yet preserving the polymeric nature of the biomass constituents. Methanol coagulated films exhibit a cocontinuous 3D-network structure with dispersed domains of less than 100 nm...

© 2017 American Chemical Society. We have prepared composite materials of hexagonal nickel phosphide and molybdenum carbide (Mo2C) utilizing a simple and scalable two-stage synthesis method composed of carbothermic reduction followed by hydrothermal incubation. We observe the monophasic hexagonal phosphide Ni2P in the composite at low phosphide-to-carbide (P:C) ratios. Upon an increase in the proportion of P:C, the carbide surface becomes saturated, and we detect the emergence of a second hexagonal nickel phosphide phase (Ni5P4) upon annealing. We demonstrate that vapor-phase upgrading (VPU) of whole biomass via catalytic fast pyrolysis is achievable using the composite material as a catalyst, and we monitor the resulting product slates using pyrolysis-gas chromatography/mass spectrometry. Our analysis of the product vapors indicates that variation of the P:C molar ratio in the composite material affords product slates of varying complexity and composition, which is indicated by the number of products and their relative proportions in the product slate. Our results demonstrate that targeted vapor product composition can be obtained, which can potentially be utilized for tuning of the composition of the bio-oil downstream.