Enhancement of the mechanical properties and water barrier properties of thermoplastic starch nanocomposite films by chitin nanofibers: Biodegradable coating for extending banana shelf life

Starch-based films have limited applications due to their hydrophilicity and poor mechanical performance. Herein, thermoplastic starch (TPS) nanocomposite films with chitin nanofibers (ChNFs) extracted from shrimp-shell waste were successfully fabricated using a solvent casting method. We investigated the effects of the ChNF loadings on the physical, mechanical, and water vapor barrier properties of the nanocomposite films. The well-dispersed ChNFs within the soft matrix associated with the formation of interfacial bonding between ChNFs and starch facilitated the efficient stress transfer from the soft matrix to the stiff ChNFs. Additionally, the presence of ChNFs created tortuous pathways within the films, which could impede the diffusion of water molecules. This resulted in a significant improvement in the mechanical properties, wettability, water resistance, and water vapor barrier properties of the nanocomposites. Compared to the results obtained from the neat TPS films, the TPS nanocomposites reinforced with ChNFs exhibited a 300% higher tensile stress, a 603% Young's modulus, and a considerable increase in the water contact angle, shifting from 86.2° to 98.6°. Furthermore, the ChNF-reinforced nanocomposite films showed no fragmentation after being soaked in water for 12 h under vigorous stirring, whereas the neat TPS films disintegrated under the same conditions. Interestingly, we found that coating a suspension of TPS and ChNFs on bananas effectively delayed their aging, preventing the color change from green to yellow. This promising result demonstrates the potential of the developed coating to extend the shelf life of fresh food produce, reducing food waste and the reliance on single-use petroleum-based packaging

Preparation of Chitin Nanofibers from Shrimp Shell Waste by Partial Deacetylation and Mechanical Treatment

Chitin is one of the most abundant biopolymers in nature. Herein, we report the successful preparation of chitin nanofibers (ChNFs) from shrimp shell waste using a partial deacetylation process with NaOH and high-speed blending. The effects of the deacetylation reaction with NaOH concentrations (0–40 wt%) on the degree of acetylation (DA), crystallinity, zeta potential, thermal stability, and morphology of the ChNFs were investigated. With the more aggressive deacetylation reaction (higher NaOH concentration), ChNFs had the lower DA, crystallinity degree, and thermal stability, and their widths and lengths became smaller and shorter. The presence of amino groups in the chitin molecule caused by deacetylation generated repulsive forces with aids of acetic acid, efficiently leading to the individualization of ChNFs using high-speed blending. The individualized ChNFs deacetylated with 30 wt% NaOH had an average width of 8.07 ± 1.80 nm and length of less than 500 nm, whereas bundles of aggregated fibers with widths in the range of 30–100 nm and lengths of up to several μm were extracted from chitin without deacetylation. Additionally, the deacetylation with 40 wt% NaOH completely converted chitin to chitosan. The ChNFs could be efficiently used for composites, biomaterials, and packaging applications

Use of TBzTD as Noncarcinogenic Accelerator for ENR/SiO2 Nanocomposites: Cured Characteristics, Mechanical Properties, Thermal Behaviors, and Oil Resistance

This study reported the use of tetrabenzylthiuram disulphide (TBzTD) as a noncarcinogenic accelerator in a traditional sulfur curing system of epoxidized natural rubber (ENR)/nanosilica (nSiO2) composites. ENR used in this work was synthesized via in situ epoxidation of natural rubber (NR) in the presence of performic acid generated from the reaction of formic acid and hydrogen peroxide at 50°C for 8 h to acquire the epoxide content of about 40 mol%. Accordingly, the resulting ENR was referred to as ENR 40. The curing characteristics, mechanical properties, thermal behaviors, dynamic mechanical properties, and oil resistance of ENR 40/nSiO2 nanocomposites filled with three loadings of nSiO2 (1, 2, and 3 parts per hundred parts of rubber) were investigated and compared with NR and neat ENR 40. The results revealed that the scorch and cure times of ENR 40/nSiO2 nanocomposites were slightly longer than those of NR but slightly shorter than those of ENR 40. The tensile properties and tear strength for both before and after aging of all ENR 40/nSiO2 nanocomposites were higher than those of ENR 40, while the glass transition temperature, storage modulus at −65°C, thermal stability, and oil resistance of ENR 40/nSiO2 nanocomposites were higher than those of NR and ENR 40

Nanocomposites of NR/SBR Blend Prepared by Latex Casting Method: Effects of Nano-TiO2 and Polystyrene-Encapsulated Nano-TiO2 on the Cure Characteristics, Physical Properties, and Morphology

Nanocomposites of 80/20 (w/w) natural rubber (NR)/styrene butadiene rubber (SBR) blend with four loadings of either nanosized titanium dioxide (nTiO2) or polystyrene-encapsulated nTiO2 (PS-nTiO2), ranging from 3 to 9 parts by weight per hundred of rubber (phr), were prepared by latex casting method. The PS-nTiO2 synthesized via in situ differential microemulsion polymerization displayed a core-shell morphology (nTiO2 core and PS shell) with an average diameter of 42 nm. The cure characteristics (scorch time, cure time, and cure rate index), mechanical properties (tensile properties, tear strength, and hardness), thermal stability, glass transition temperature, and morphology of the prepared nanocomposites were quantified and compared. The results showed that the cure characteristics of all the nanocomposites were not significantly changed compared to those of the neat NR/SBR blend. The inclusion of an appropriate amount of either nTiO2 or PS-nTiO2 into the NR/SBR blend apparently improved the tensile strength, modulus at 300% strain, tear strength, hardness, and thermal stability but deteriorated the elongation at break of the nanocomposites. Based on differential scanning calorimetry, the glass transition temperature of all the nanocomposites was similar to that of the neat NR/SBR blend. Moreover, the morphology of the PS-nTiO2-filled rubber nanocomposites fractured surface analyzed by scanning electron microscopy showed an improvement in the interfacial adhesion between the rubber phase and the nanoparticles