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Polymer composites from polylactic acid (PLA) and two types of cellulose fibers obtained either by acid hydrolysis of microcrystalline cellulose (HMCC) or by mechanical disintegration of regenerated wood fibers (MF) were prepared and characterized. To enhance the compatibility of the cellulose fibers with PLA matrix, a surface treatment based on 3‐aminopropyltriethoxysilane (APS) was performed. The Fourier Transform Infrared (FTIR) spectroscopy was used to determine the chemical groups involved in the surface modification reaction. The silanization treatment resulted in different modifications on both types of cellulose fibers because of their different structural and morphological characteristics. The composites were prepared by incorporating 2.5% of the treated or untreated HMCC and MF into a PLA matrix using a melt‐compounding technique. An improved adhesion between the two phases of the composite materials was observed by scanning electron microscopy thanks to treatment. The dynamic mechanical thermal analyses showed that both untreated and silane treated fibers led to an improvement of the storage modulus of PLA in the glassy state. A higher enhancement of the storage modulus in the case of PLA/HMCC composites than the composites containing MF was obtained as a result of the high aspect ratio of these fibers which allows better matrix‐to‐filler stress transfer. Furthermore, the storage modulus of PLA composites was enhanced by silanization even at higher temperatures especially after thermal treatment. The cellulose fibers addition in PLA matrix modified significantly the relaxation phenomenon as observed in tan δ curves, emphasizing strongly modified molecular mobility of PLA macromolecules and crystallization changes. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers.

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a b s t r a c tThe mechanical properties of sulfonated aromatic polymers (SAPs: SPEEK and SPPSU) are studied by tensile stress-strain tests and dynamic mechanical analysis (DMA). The elastic moduli are generally above 1 GPa with tensile strength between 25 and 80 MPa and elongation at rupture between 7 and 50%. These properties are consistent with polymers below their glass transition temperature. The glass transition and elastic moduli are strongly increased by thermal treatments of the SAP membranes, due to formation of cross-links between macromolecules. The cross-linking is observed "in situ" during DMA experiments on thermally untreated SPPSU. These data show that previously neglected SAPs might become very interesting PEM fuel cell membranes, if previously thermally treated.