Thermal forming of chemically modified wood to make high-performance plastic-like wood composites
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Abstract
Chemically modified wood composites were obtained via the compression moulding of thermoplasticised Aspen (Populus tremula) sawdust. This sawdust was previously prepared by esterification with maleic anhydride (MA) and subsequent oligoesterification with maleic anhydride and glycidyl methacrylate (GMA). The thermoplastic properties of the chemically modified wood resulting from different modification procedures were confirmed and compared by compression-moulding experiments leading to preliminary and final products. An SEM study of the resulting products clearly showed that the oligoesterified wood had partially melted under pressure and temperature, such that the overlapping and surface melting of particles ensured adhesive bonding between those particles. A new type of wood/thermoplastic-wood composite was obtained. In these composites, the melted part of the modified wood plays the role of the cohesive matrix whilst none-melted wood remains as a fibrous reinforcing material. FTIR spectra suggested that changes in the chemical structure of the modified wood are possible during the thermal forming process (e.g. polymerisation of C=C double bonds).
The final composites were yellowish-brown, glossy, plastic-like products that showed interesting physical, mechanical and biological properties. They are water-resistant and dimensionally stable and display good electrical insulating behaviour. Their mechanical properties (bending strength of ca. 64 MPa and tensile strength of ca. 36 MPa) are in the typical range for plastics and conventional wood-fibre/plastic composites, and are superior to common wood products such as fibreboards and particleboards. Furthermore, the outstandingly high internal bond (ca. 3.0 MPa) highlights the totally different adhesion mechanism operating in these new types of composites. Although the novel composites are much more resistant to decay than the original unmodified wood, they remain ultimately biodegradable plastic-like composites.
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© Walter de Gruyter
Articles in the same Issue
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Articles in the same Issue
- The effects of initial spacing on wood density, fibre and pulp properties in jack pine (Pinus banksiana Lamb.)
- An improved procedure for isolation of residual lignins from hardwood kraft pulps
- Small angle scattering in the Porod region from hydrated paper sheets at varying humidities
- Application of confocal Raman spectroscopy for the topochemical distribution of lignin and cellulose in plant cell walls of beech wood (Fagus sylvatica L.) compared to UV microspectrophotometry
- UV-microscopic analysis of acetylated spruce and birch cell walls
- On-line study of lignin behaviour in dilute alkaline solution by the SEC-UV method
- Extracellular diffusion pathway for heartwood substances in Albizia julibrissin Durazz.
- New glucosides from Eucalyptus globulus wood, bark and kraft pulps
- Nondestructive characterization of wood by monitoring of local elastic anisotropy and dynamic nonlinearity
- Chemical reaction of maritime pine sapwood (Pinus pinaster Soland) with alkoxysilane molecules: A study of chemical pathways
- Thermal forming of chemically modified wood to make high-performance plastic-like wood composites
- Eco-composite from poly(lactic acid) and bamboo fiber
- Bamboo fiber (BF)-filled poly(butylenes succinate) bio-composite – Effect of BF-e-MA on the properties and crystallization kinetics
- Dimensional changes in Corsican pine (Pinus nigra Arnold) modified with acetic anhydride measured using a helium pycnometer
- Microwave-enhanced release of formaldehyde from plywood
- Artificial weathering of tropical woods. Part 1: Changes in wettability
- Artificial weathering of tropical woods. Part 2: Color change
- Inhibition of fungal degradation of wood by 2-hydroxypyridine-N-oxide
- Microwave treatment to accelerate fixation of copper-ethanolamine (Cu-EA) treated wood