The composite alpaca/acrylic fibers were auspiciously produced through a wet spinning technique to reduce the consumption of petroleum-based polyacrylonitrile (PAN) and to enhance the thermal stability and moisture properties of the fibers. The waste alpaca fibers were converted into powder using a mechanical milling method without applying any chemicals. Alpaca powders were then blended with the PAN dope solution in different weight ratios of alpaca: PAN (10:90, 20:80, and 30:70) to wet spin the composite fibers. The Fourier transform infrared spectroscopy showed that all the composite fibers possess the functional groups of both alpaca and PAN. The nuclear magnetic resonance spectroscopy confirmed the presence of typical carbonyl carbon (C O) and nitrile carbon (C≡N) peaks of protein and PAN, respectively. The differential scanning calorimetry and thermogravimetric analysis revealed the enhanced thermal stability of alpaca/PAN composite fibers. The moisture properties of the composite fibers were subsequently found to increase with the incorporation of alpaca, more than three times that of pure PAN fibers. These results revealed a potential green pathway to producing composite acrylic fibers with improved thermal and moisture properties by applying textile waste materials.

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This work proposes a new approach to fabricate highly transparent and flexible composite films that exhibit enhanced UV-shielding properties. Lignin has innate UV-shielding properties. However, when purified lignin, which is conventionally extracted through chemical treatment, is mixed with polymeric materials, its presence negatively influences the transparency of the resulting composite. High transparency and UV-shielding are desirable properties for many applications. In this study, composites were made by mixing lignocellulose particles and polyvinyl alcohol (PVA), where lignocellulose particles were obtained from ball-milled waste hemp hurd without chemical treatments. The UV-shielding properties of the resulting composite film, as a function of hemp/PVA weight ratios, were investigated. The intermolecular interactions between the hemp particles and the PVA were characterized using infrared spectroscopy with the presence of –C=O group at 1655 cm−1, providing evidence that the chemical structure of lignin was preserved. The fabricated hemp/PVA films exhibit stronger UV-shielding, in the UVA-I range (340–400 nm) than TiO2/PVA films. The composite films also showed comparable water vapor permeability (WVP) with commercial packaging plastic film made of HDPE (high-density polyethylene). The optimization experiments were reported, with aim at understanding the balance between the UV-shielding and mechanical properties of the hemp/PVA films. The findings of this work can be applicable to the packaging, food and cosmetic industries where UV shielding is of utmost importance, hence adding value to hemp hurd waste.

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The study examined the effect of different wet spinning parameters (e.g., total solid content, coagulation bath concentration, drawing, and stretching) on the morphology and mechanical properties of the wet spun alpaca/polyacrylonitrile (PAN) composite fibers. The alpaca/PAN composite fibers were wet spun using 10, 20, and 30% of alpaca particles along with the PAN polymer. The shear‐thinning or non‐Newtonian flow behavior was observed among the dope solutions with different solid content. The cross‐sectional fiber morphology showed the bean‐shaped characteristic for the control PAN fibers, whereas the alpaca/PAN composite fibers exhibited almost circular shape. “Cavity healing” was observed, where noticeable voids and porous areas were demolished in the cross section of the composite fibers, by changing the total solid content and coagulation bath concentration. Although the control PAN fibers exhibited the highest tenacity with lower fiber diameter, the alpaca/PAN composite fibers showed a gradual deterioration in tenacity while adding alpaca particles into the PAN polymeric matrix. Nevertheless, due to the increment in the total solid content, higher draw ratio, and stretching of the fibers, the tenacity, molecular orientation, and the crystallinity of the composite fibers were increased.

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This work aims to evaluate the potential of using textile waste in smart textile applications in the form of a hybrid fibre with electrical properties. The bio-based electrically conductive fibres were fabricated from waste wool and polyacrylonitrile (PAN) via wet spinning with different wool content. The control PAN and hybrid fibre produced with the highest amount of wool content (25% w/v) were coated with graphene oxide (GO) using the "brushing and drying" technique. The GO nanosheets coated control PAN and wool/PAN hybrid fibres were chemically reduced through hydrazine vapour exposure. The Fourier transform infrared spectroscopy showed the presence of both protein and nitrile peaks in the wool/PAN hybrid fibres, although the amide I and amide A groups had disappeared, due to the dissolution of wool. The morphological and structural analysis revealed effective coating and reduction of the fibres through GO nanosheets and hydrazine, respectively. The hybrid fibre showed higher electrical conductivity (~ 180 S/cm) compared to the control PAN fibres (~ 95 S/cm), confirming an effective bonding between the hydroxyl and carboxylic groups of the GO sheets and the amino groups of wool evidenced by chemical analysis. Hence, the graphene oxide incorporated wool/PAN hybrid fibres may provide a promising solution for eco-friendly smart textile applications.