Because of the increasing awareness of the environment and energy issues, as well as advances in technology, the areas of application for annual plant fiber functional materials are expanding. In this work, two chemical treatments, alkalization (2 h agitation with 5% NaOH) and furfurylation (graft furfuryl alcohol followed by oxidation with (1N) NaClO 2 solution), were conducted on Luffa cylindrica fiber surfaces. The grafting of furfuryl alcohol followed by oxidation-generated quinines showed better results than alkaline treatment with respect to enhancement of surface area and hydrophobicity as well as wax, lignin, and hemicellulose extraction. The efficiency of chemical treatments was verified by elemental analysis and FTIR spectroscopy. Differential scanning calorimetry, thermo-gravimetric analysis, scanning electron microscopy, water absorption, and mechanical tests were performed to determine the thermal, mechanical, and morphological properties of untreated and chemically treated luffa fiber reinforced epoxy composites. Microstructures of the composites were examined to determine the mechanisms for the fiber-matrix interaction, which affects the thermal stability, water absorption, and mechanical behavior of the composites. The data from the water absorption process of composites at various temperatures were analyzed using a diffusion model based on Fick's law.

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In this study, the effects of fiber surface modification and hybrid fiber composition on the properties of the composites is presented. Jute fibers are cellulose rich (>65%) modified by alkali treatment, while the lignin rich (>40%) coconut coir fibers consist in creating quinones by oxidation with sodium chlorite in the lignin portions of fiber and react them with furfuryl alcohol (FA) to create a coating around the fiber more compatible with the epoxy resins used to prepare polymer composites. The maximum improvement on the properties was achieved for the hybrid composite containing the jute-coir content of 50 : 50. The tensile and flexural strength are recorded as 25 and 63 MPa at modified coir fiber content of 50 vol %, respectively, which are 78% and 61% higher than those obtained for unmodified fiber reinforced composites, i.e., tensile and flex-ural strength are 14 and 39 MPa, respectively. The reinforcement of the modified fiber was significantly enhanced the thermal stability of the composites. SEM features correlated satisfactorily with the mechanical properties of modified fiber reinforced hybrid composites. SEM analysis and water absorption measurements have confirmed the FA-grafting and shown a better compatibility at the interface between chemically modified fiber bundles and epoxy novolac resin. Hailwood-Horrobin model was used to predict the moisture sorption behavior of the hybrid composite systems.

In this study, randomly oriented short jute/bagasse hybrid fiber‐reinforced epoxy novolac composites were prepared by keeping the relative volume ratio of jute and bagasse of 1:3 and the total fiber loading 0.40 volume fractions. The effect of jute fiber hybridization and different layering pattern on the physical, mechanical, and thermal properties of jute/bagasse hybrid fiber‐reinforced epoxy novolac composites was investigated. The hybrid fiber‐reinforced composites exhibited fair water absorption and thickness swelling properties. To investigate the effect of layering pattern on thermomechanical behavior of hybrid composites, the storage modulus and loss factor were determined using dynamic mechanical analyzer from 30 to 200°C at a frequency of 1 Hz. The fracture surface morphology of the tensile samples of the hybrid composites was performed by using scanning electron microscopy. The morphological features of the composites were well corroborated with the mechanical properties. Thermogravimetric analysis indicated an increase in thermal stability of pure bagasse composites with the incorporation of jute fibers. The incorporation of hybrid fibers results better improvement in both thermal and dimensional stable compared with the pure bagasse fiber composites. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers

Vectra | liquid crystalline polymers (LCP's) were introduced as commercial products in the mid-1980's. The first of these (Vectra A130) was a wholly aromatic thermotropic copolyester of p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid. Vectra A130 is a thermotropic LCP that can be melt spun into filaments that on heat treatment are characterized by high strength and high modulus. Vectra resin can also be extruded into films. In the fiber or film form this material is commercially known as Vectran | Heat treatment enhances the tensile strength of Vectran fiber variants. Because of this, the elucidation of the physical transformations taking place in the internal structure of the material during heating has always been an important subject. Several thermal techniques are used to indicate clearly that what is observed as a "glass transition" is unlike the conventional glass transition in typical semicrystalline polymers. There is also an indication of the presence of multiple states of mesophase aggregation that collapse into a single state when taken to high enough temperatures.