Effects of wood fiber surface chemistry on strength of wood–plastic composites
- 1. University of Quebec in Abitibi-Temiscamingue (UQAT), 445 boulevard de l'Université, Rouyn-Noranda, Québec J9X 5E4 (Canada)
- 2. UQAT (Canada)
- 3. École centrale de Paris, Grande Voie des Vignes, F-92 295 Chatenay-Malabry Cedex (France)
- 4. Université Laval, 2425 rue de la Terrasse, Québec City, Québec G1V 0A6 (Canada)
Description
Highlights: • Infrared spectroscopy and X-ray photoelectron spectroscopy analyses showed variations of surface chemical characteristics according to fiber origin. • Surface chemical characteristics of fibers could partly explain the differences in mechanical properties of the wood–plastic composites. • Fibers with carbohydrate rich surface led to stronger wood–plastic composites because the coupling between the matrix and fibers using coupling agent is achieved with polar sites mostly available on carbohydrates. • Conversely, lignin or extractives rich surface do not have oxidized functions for the esterification reaction with coupling agent and thus led to wood–plastic composites with lower mechanical properties. • Other factors such as mechanical interlocking and fiber morphology interfere with the effects of fiber surface chemistry. - Abstract: Because wood–plastic composites (WPC) strength relies on fiber-matrix interaction at fiber surface, it is likely that fiber surface chemistry plays an important role in WPC strength development. The objective of the present study is to investigate the relationships between fiber surface chemical characteristics and WPC mechanical properties. Different fibers were selected and characterized for surface chemical characteristics using X-ray photoelectron spectroscopy (XPS) and infrared spectroscopy (FTIR). WPC samples were manufactured at 40% fiber content and with six different fibers. High density polyethylene was used as matrix and maleated polyethylene (MAPE) was used as compatibility agent. WPC samples were tested for mechanical properties and fiber-matrix interface was observed with scanning electron microscope. It was found WPC strength decreases as the amount of unoxidized carbon (assigned to lignin and extractives) measured with XPS on fiber surface increases. In the opposite case, WPC strength increases with increasing level of oxidized carbon (assigned to carbohydrates) on fiber surface. The same conclusions were found with FTIR where WPC strength decreases as lignin peaks intensity increases. Esterification reaction of fibers with MAPE occurs on polar sites of carbohydrates, such as hydroxyls (O−H). Thus, fibers with carbohydrates-rich surface, such as cellulose pulp, produced stronger WPC samples. Other factors such as mechanical interlocking and fiber morphology interfered with the effects of fiber surface chemistry
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2015.03.010Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2015.03.010;
- PII
- S0169-4332(15)00546-2;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 343
- Journal Page Range
- p. 11-18
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47037800
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; ADHESION; CARBON; CELLULOSE; COUPLING; DENSITY; FIBERS; FOURIER TRANSFORMATION; HYDROXIDES; INFRARED SPECTRA; INTERACTIONS; INTERFACES; LIGNIN; PLASTICS; POLYETHYLENES; SCANNING ELECTRON MICROSCOPY; SURFACES; WOOD; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CARBOHYDRATES; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; HYDROGEN COMPOUNDS; INTEGRAL TRANSFORMATIONS; MATERIALS; MICROSCOPY; NONMETALS; ORGANIC COMPOUNDS; ORGANIC POLYMERS; OXYGEN COMPOUNDS; PETROCHEMICALS; PETROLEUM PRODUCTS; PHOTOELECTRON SPECTROSCOPY; PHYSICAL PROPERTIES; POLYMERS; POLYOLEFINS; POLYSACCHARIDES; SACCHARIDES; SPECTRA; SPECTROSCOPY; SYNTHETIC MATERIALS; TRANSFORMATIONS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.