ABSTRACT
The viability of single-step microwave-induced pressurized hot water conditions for co-production of xylan-based biopolymers and bioethanol from aspenwood sawdust and sugarcane trash was investigated. Extraction of hemicelluloses was conducted using microwave-assisted pressurized hot water system. The effects of temperature and time on extraction yield and enzymatic digestibility of resulting solids were determined. Temperatures between 170-200°C for aspenwood and 165-195°C for sugarcane trash; retention times between 8-22min for both feedstocks, were selected for optimization purpose. Maximum xylan extraction yields of 66 and 50%, and highest cellulose digestibilities of 78 and 74%, were attained for aspenwood and sugarcane trash respectively. Monomeric xylose yields for both feedstocks were below 7%, showing that the xylan extracts were predominantly in non-monomeric form. Thus, single-step microwave-assisted hot water method is viable biorefinery approach to extract xylan from lignocelluloses while rendering the solid residues sufficiently digestible for ethanol production.
Subject(s)
Microwaves , Polysaccharides , Cellulose , Hot Temperature , Hydrolysis , WaterABSTRACT
Wood fibres have been utilized by our society as an important component of paper products and are presently gaining more interest as reinforcement in composite materials. During the last decades biochemical treatments have also found applications in the processing of wood fibres. The chemical, mechanical and biochemical treatments affect the morphology of the fibre wall structure at the micro- and nano-level. In this study, we present a modern approach where field-emission SEM (FE-SEM) and relevant computerized image analysis are applied to quantify the fibre wall characteristics. Details such as surface roughness and texture of the fibre walls are quantified objectively. Global polar plots are generated, which are considered to represent the fingerprint of a given pulp. The approach offers a novel perspective in the characterisation of surface structures, moving forward from performing subjective evaluations to performing objective quantifications of wood pulp fibre surfaces.
Subject(s)
Enzymes/metabolism , Wood/metabolism , Wood/ultrastructure , Image Processing, Computer-Assisted , Microscopy, Electron, Scanning , Surface PropertiesABSTRACT
The content and distribution of stilbenes and resin acids in Scots pine (Pinus sylvestris) and spruce (Picea abies), sampled in central Norway, have been examined. The contents of pinosylvin stilbenes in pine heartwood/living knots were 0.2-2/2-8 %(w/w). No stilbenes could be detected in spruce (Picea abies). The resin acid contents of pine sapwood/heartwood and knots were 1-4 and 5-10 % (w/w), respectively. Minor amounts of resin acids (<0.2/<0.04 %w/w) were identified in spruce wood/knots. The lignan content in knots of Norwegian spruce was 6.5 % (w/w). Diastereomerically pure hydroxymatairesinol (HMR, 84 % of total lignans) was readily isolated from this source since only minor quantities (2.6 % of total lignans) of the allo-HMR diastereomer was detected. Insignificant amounts of lignans were present in the sapwood. Lignans could not be detected in the sapwood or knots of Norwegian sallow (Salix caprea), birch(Betula pendula) or juniper (Juniperus communis).