Composites based on phenolic matrices and unmodified and chemically modified sugar cane bagasse and curaua fibers were prepared. The fibers were oxidized by chlorine dioxide, mainly phenolic syringyl and guaiacyl units of the lignin polymer, followed by grafting furfuryl alcohol (FA), which is a chemical obtained from a renewable source. The fibers were widely characterized by chemical composition analysis, crystallinity, UV-vis diffuse reflectance spectroscopy, SEM, DSC, TG, tensile strength, and 13C CP-MAS NMR. The composites were analyzed by SEM, impact strength, and DMA. The SEM images and DMA results showed that the oxidation of sugar cane bagasse fibers followed by reaction with FA favored the fiber/matrix interaction at the interface. The same chemical modification was less effective for curaua fibers, probably due to its lower lignin content, since the reaction considered touches mainly the lignin moiety. The tensile strength results obtained showed that the fibers were partially degraded by the chemical treatment, decreasing then the impact strength of the composites reinforced with them. In the continuity of the present project, efforts has been addressed to the optimization of fiber surface modification, looking for reagents preferably obtained from renewable resources and for chemical modifications that intensify the fiber/matrix interaction without loss of mechanical properties.

ABSTRACT:Composites based on phenolic matrices and both untreated and alkali and ionized air-treated jute fibers were prepared. Different fiber lengths and fiber content were used to reinforce the phenolic matrices. The jute fibers were characterized with respect to lignin, holocellulose, ash, and humidity contents and also to the crystallinity index. The mechanical properties of fibers were investigated by means of tensile analysis and the morphology by SEM. The untreated and treated jute fiber-reinforced composites were characterized as to water absorption. The mechanical property and morphological aspects of the composites were evaluated by impact strength and photomicrographs obtained from SEM. Among the jute fiber treatments considered in the present work, the treatment with a solution of 5% NaOH presented the best results because: (1) the fiber presented a higher tensile strength, and a larger percentage of elongation at break; (2) the composite reinforced with this fiber presented the highest impact strength results when this was the unique treatment (20% of fiber), as well as when it was combined with ionized air (30% of fiber); and (3) the composite that presented the lowest water uptake was that reinforced with this fiber.

Summary: A new chemical modification of sugar cane bagasse fibers for phenolic thermoset composites is presented. It consists in creating quinones in the lignin portions of fiber and react them with furfuryl alcohol to create a coating around the fiber more compatible with the phenolic resins used to prepare polymeric matrix. Sodium periodate was used in suitable conditions to oxidize mainly phenolic syringyl and guaiacyl units of the lignin polymer to create quinones, which were characterized by UV‐visible diffuse reflectance spectroscopy by comparison with model compounds. The reactivity of furfuryl alcohol (FA) with fibers was greatly enhanced after they were oxidized: 13% weight percent gain compared to 2% without oxidation. Chemical analysis of unmodified and FA‐modified fibers have shown an important degradation of hemicelluloses and a slight one of cellulose which almost maintains its crystallinity. A 25% decrease of strength and length properties of the fibers after FA chemical treatment was measured by dynamic mechanical analysis. The lignin‐like proportion of the fiber was greatly enhanced after the FA‐treatment. This was confirmed by thermal analysis, DSC, and TGA experiments, on unmodified and FA‐modified fibers. SEM analysis of the fibers and of phenolic composites with modified fibers have confirmed the FA grafting and shown a better compatibility at the interface between the chemically modified fibers and the phenolic matrix. Nevertheless, the chemical treatment of the fibers decreased the impact strength of the composite, which could be caused by the fiber damage suffered during the chemical modification and for the more intense adhesion at the interface, which in some cases decrease somewhat the impact strength.Cross photomicrography of FA‐modified sugar cane bagasse fiber (600×).magnified imageCross photomicrography of FA‐modified sugar cane bagasse fiber (600×).

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