Modification of nanocellulose filler via amination and subsequent grafting of gallic acid for enhancing the performance of biodegradable soy protein films in banana packaging
Abstract
The excessive use of petroleum-based packaging necessitates the need for sustainable, biodegradable alternatives. This study developed a high-performance active packaging film by incorporating chemically modified cellulose nanocrystals (CNCs) into a soy protein isolate (SPI) matrix. CNCs were functionalized via silanization with 3-aminopropyltriethoxysilane (APTES) followed by covalent gallic acid grafting. Compared to glycerol-plasticized SPI, the composite films showed significantly enhanced mechanical strength (237.3% increase in tensile strength, from 2.17 to 7.32 MPa), improved water vapor barrier (30.16% reduction in permeability), nearly 100% UV blocking at 200–350 nm, antioxidant activity (12.4% DPPH scavenging), and antibacterial properties. In a 7-day banana preservation test, the optimized film effectively delayed weight loss, softening, and browning while remaining biodegradable, showing visible degradation within 20 days in soil. This work demonstrates a feasible interfacial design strategy for developing multifunctional SPI-based nanocomposite films with high potential for fresh-keeping packaging of perishable fruits such as bananas. • A biodegradable film based on soy protein with enhanced performance was prepared. • Silanized bamboo CNCs-GA boosted SPI film strength by 237% (from 2.17 to 7.32 MPa). • SPI/CNCs composite film shows visible degradation after 20 days of soil burial. • It provided nearly 100% UV absorption at 200–350 nm. • SPI/CNCs composite film significantly inhibits the browning process of bananas during the 7-day storage period.
Fields of Study & Subjects
Nanocomposite Films for Food Packaging
Advanced Cellulose Research Studies
Natural Fiber Reinforced Composites
Publication details
- Journal / source
- Food Chemistry X
- Publisher
- Elsevier BV
- Volume
- 35
- Pages
- 103705–103705
- Publication date
- 25 February 2026
- Language
- EN