Natural fiber composites are known to absorb more water than glass fiber reinforced composites. In this study, hybrid natural fiber composites were prepared by combining different fiber reinforcements, and both the water absorption and the mechanical properties were studied. Compression molding technique was used to manufacture composite laminates from a bio-based resin (acrylated epoxidized soybean oil) and natural fibers: non-woven and woven jute, non-woven regenerated cellulose mat (Lyocell and viscose), and woven glass fiber. The composite laminates were cured at 160–170 C and 40 bar, with a fiber content of 40 wt%. We investigated effect of pretreatment of regenerated cellulose fiber using 4% NaOH solution. The gravimetric water absorption was tested by exposure to water for 10 days. Specimens were cut from composites with laser-cutting technique according to ISO standards, and tested for tensile, flexural, and impact strength. To determine the influence of water absorption on the mechanical properties, specimens were immersed in distilled water for 10 days before testing. As a reference, dry specimens were tested. The results showed that water absorption was reduced by producing hybrid composites with jute fibers, glass fiber, and Lyocell fiber. The tensile, flexural, and impact properties were improved by inclusion of glass fiber and Lyocell in the composite. The tensile and flexural properties of natural fiber reinforced composites were mostly affected by the influence of water, but this was improved considerably by hybridization with glass and Lyocell fibers. The viscoelastic properties of the manufactured composites and hybrid composites were studied using dynamic mechanical thermal analysis.

The effect of surface treatments, silane and alkali, on regenerated cellulose fibers was studied by using the treated fibers as reinforcement in lactic acid thermoset bioresin. The surface treatments were performed to improve the physico–chemical interactions at the fiber–matrix interface. Tensile, flexural and impact tests were used as indicator of the improvement of the interfacial strength. Furthermore, thermal conductivity, viscoelasticity measurements as well as microscopy images were made to characterize the fiber surface treatments and the effect on adhesion to the matrix. The results showed that silane treatment improved the mechanical properties of the composites as the silane molecule acts as link between the cellulose fiber and the resin (the fiber bonds with siloxane bridge while the resin bonds with organofunctional group of the bi-functional silane molecule) which gives molecular continuity in the interphase of the composite. Porosity volume decreased significantly on silane treatment due to improved interface and interlocking between fiber and matrix. Decrease in water absorption and increase in contact angle confirmed the change in the hydrophilicity of the composites. The storage modulus increased when the reinforcements were treated with silane whereas the damping intensity decreased for the same composites indicating a better adhesion between fiber and matrix on silane treatment. Thermogravimetric analysis indicated that the thermal stability of the reinforcement altered after treatments. The resin curing was followed using differential scanning calorimetry and the necessity for post-curing was recommended. Finite element analysis was used to predict the thermal behavior of the composites and a non-destructive resonance analysis was performed to ratify the modulus obtained from tensile testing. The changes were also seen on composites reinforced with alkali treated fiber. Microscopy images confirmed the good adhesion between the silane treated fibers and the resin at the interface.

Composites were developed by reinforcing available non-woven Lyocell and viscose in acrylated epoxidized soybean oil (AESO). Compression molding was used to make composites with 40–60 wt% fiber content. The fiber content comprises only Lyocell or viscose fiber, or mixture of these fibers in known ratio. Hybrid composites were made by a mixture of both the fibers in known ratio and it affects the properties. The effect of hybridization was evident in most tests which gives us an opportunity to tailor the properties according to requirement. Lyocell fiber reinforced composites with 60 wt% fiber content had a tensile strength and modulus of about 135 MPa and 17 GPa, respectively. Dynamic mechanical analysis showed that the Lyocell fiber reinforced composites had good viscoelastic properties. The viscose fiber reinforced composites had the high percentage elongation and also showed relatively good impact strength and flexural modulus. Good fiber-matrix adhesion reflected in mechanical properties. SEM images were made to see the fiber-matrix compatibility.

Polyester (PET) has wide applications in textile industries as textile fiber and its share continues to grow. Substantial quantities of cotton/polyester blend fabrics are disposed every year due to technical challenges, which pose a big environmental and waste-dumping problem. The aim of this study is to evaluate the potential of discarded cotton/PET fabrics as raw materials for composites. If their inherent reinforcement properties can be used in composites, an ecological footprint issue can be solved. In this study, we investigate three concepts for reuse of cotton/PET fabrics for composites: compression molding above the Tm of PETs, use of a matrix derived from renewable soybean oil, use of thermoplastic copolyester/polyester bi-component fibers as matrix. All three concepts have been explored to make them available for wider applications. The effects of processing parameters such as compression temperature, time and pressure are considered in all three cases. The third concept gives the most appealing properties, which combine good tensile properties with toughness; more than four times better tensile strength than the first concept; and 2.2 times better than the second concept.

Cellulose fibres have significant importance and potential for polymer reinforcement. It is essential to modify the surface of the fibre to obtain good fibre-matrix interface. Surface treatments can increase surface roughness of the fibre, change its chemical composition and introduce new moieties that can effectively interlock with the matrix, resulting in good mechanical properties in the composites. This is mainly due to improved fibre-matrix adhesion. The treatments may also reduce the water absorption rate by converting part of the hydroxyl groups on the fibre surface into other functional groups. Chemical modification of the surface of a regenerated cellulose fibre of the Lyocell type was carried out by alkali and silane treatments, which significantly changed the properties of the Lyocell fibres. Three parameters were considered when the fibre surface treatment was done: concentration (2–15 wt%), temperature (25 and 50 C) and time (30 min–72 h). Fourier transform infrared spectroscopy and Raman spectroscopy were used for chemical analysis and qualitative analysis of the cellulose crystallinity due to the surface treatments; subsequently, mechanical strength of the fibres was tested by tensile testing. Weight loss, moisture regain and swelling measurements were taken before and after treatments, which showed the obvious changes in fibre properties on treatment. Heat capacity of the fibres was measured for untreated and treated fibres, and thermal degradation of fibres was examined to see the stability of fibres at elevated temperatures. Wettability and surface energies were measured using dynamic contact angle method in three wetting mediums. Scanning electron microscopy was used to study the morphological properties of the fibres.