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Kenaf fiber‐reinforced copolyester biocomposites
Author(s) -
Mokhothu T.H.,
Guduri B.R.,
Luyt A.S.
Publication year - 2011
Publication title -
polymer composites
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.577
H-Index - 82
eISSN - 1548-0569
pISSN - 0272-8397
DOI - 10.1002/pc.21233
Subject(s) - materials science , copolyester , thermogravimetric analysis , composite material , kenaf , fiber , differential scanning calorimetry , biocomposite , ultimate tensile strength , dynamic mechanical analysis , silane , environmental scanning electron microscope , natural fiber , compatibilization , scanning electron microscope , composite number , polymer , polymer blend , chemical engineering , copolymer , polyester , physics , engineering , thermodynamics
Abstract In this study the morphology and properties of a biodegradable aliphatic–aromatic copolyester mixed with kenaf fiber were investigated. Untreated kenaf fiber, as well as kenaf fiber treated with NaOH, and with NaOH followed by silane coupling agent treatment at various concentrations, were used as fillers in the composites. The biocomposites were prepared by melt‐mixing and a 10 wt% fiber loading was used for all the composites. The properties of the biocomposites were characterized using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), tensile properties, environmental scanning electron microscopy (ESEM), and biodegradability. The extent of silane initiated grafting was followed by gel content determination. The presence of fiber and fiber treatment influenced the determined properties in a variety of ways, but the best balance of properties were found for the copolyester mixed with alkali‐treated fiber. This composite showed improved thermal, thermomechanical, and mechanical properties. The introduction of alkali treatment caused increased surface roughness in the fiber, which resulted in mechanical interlocking between the filler and the matrix, while silane treatment slightly reduced the properties. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers