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Xyloglucan films from tamarind kernels reinforced with chemically modified cellulose nanospheres

International Journal of Biological Macromolecules 2025 1 citation ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 53 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Rahul Thakur, G Sravanthi, Rahul Thakur, G Sravanthi, Tizazu H. Mekonnen, Tizazu H. Mekonnen, Tizazu H. Mekonnen, Rahul Thakur, Srinivas Janaswamy, Srinivas Janaswamy, Rahul Thakur, Sib Sankar Giri Srinivas Janaswamy, Preetam Sarkar, Thilini Dissanayake, Tizazu H. Mekonnen, Srinivas Janaswamy, Tizazu H. Mekonnen, Nandika Bandara, Kunal Pal, Sib Sankar Giri Preetam Sarkar, Sib Sankar Giri

Summary

Researchers developed biodegradable films from tamarind kernel xyloglucan reinforced with chemically modified cellulose nanospheres as an alternative to conventional plastic food packaging. The bio-based films showed improved mechanical and barrier properties, offering a renewable approach to reducing microplastic and nanoplastic generation from the food packaging sector.

Polymers
Body Systems

Globally, over 0.3 billion tons of plastic are produced each year, most of which are non-biodegradable and derived from non-renewable resources. The food packaging sector alone consumes approximately 37.3 million tons annually, contributing significantly to the proliferation of microplastics and nanoplastics, which pose serious risks to both environmental and human health. Agricultural byproducts, such as tamarind kernels, which contain approximately 70 % xyloglucan (TXG), are promising renewable feedstocks for bioplastic production. In this study, TXG was extracted and used to create biopolymer films reinforced with unmodified cellulose nanospheres (U-CNS) and TEMPO-modified cellulose nanospheres (TM-CNS). Rheological analysis of the film-forming solution showed shear-thinning behavior, while FTIR and XRD confirmed successful incorporation of U-CNS and TM-CNS into the TXG matrix. FE-SEM imaging revealed reduced nanoparticle aggregation in TM-CNS films compared with U-CNS films. Adding nanoparticles significantly improved the functional properties of TXG films. Hydrophobicity increased, with the contact angle rising from 31.7° to 81.6°, and moisture content dropped from 19.90 % to 13.69 %. Both U-CNS and TM-CNS increased the tensile strength (TS) of TXG films, raising it from 10.22 MPa to 28.31 MPa, similar to low-density polyethylene (LDPE) films (8-31 MPa). However, U-CNS reduced elongation-at-break (EAB), while TM-CNS maintained flexibility with an EAB of 53.29 % and enhanced strength. Notably, TXG films with 5 % TM-CNS achieved the lowest water vapor permeability (WVP: 2.745 g·mm/day·m·kPa). Overall, the integration of TM-CNS into TXG films significantly improved mechanical, barrier, and surface properties, demonstrating strong potential for use as sustainable, biodegradable alternatives to conventional plastic packaging.

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