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The effects of plasticizers on the mechanical properties and chemical composition of a gelatin biopolymer
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This study examined the distribution and characteristics of microplastics in beach sediments along a coastal area, finding widespread contamination with fibers and fragments of various polymer types. Polyethylene and polypropylene were the dominant polymers detected, suggesting land-based sources and ocean currents as primary transport pathways.
Every day, oil-based plastics are manufactured, consumed, and discarded without a second thought. To combat plastic pollution, we decided to investigate gelatin bioplastics. We analysed the effects of the increasing concentration of polyethylene glycol (PEG) and glycerol plasticizers on the mechanical properties and chemical composition of the gelatin bioplastic matrix through a series of experiments. In the first experiment, we determined their tensile strength (TS) and the elongation at break (EAB) through tensile testing. We hypothesised that increasing concentrations of the plasticizers would decrease TS and increase EAB. In the second experiment, we studied their O–H bonds by Fourier-transform infrared spectroscopy analysis (FTIR). Our second hypothesis maintained that the number of O–H bonds would increase because plasticizers disrupt polymer-polymer and polymer-water hydrogen bonds. For the mechanical properties, we observed that when the concentration of PEG and glycerol plasticizers increased so too did EAB. The rising concentrations of glycerol led to a decreasing trend with TS, whereas PEG showed an increasing trend. The FTIR spectrum revealed that a high abundance of O–H bonds was present at the strong and broad absorption peak of 3400 cm-1, with the pure gelatin films having the highest absorption, followed by glycerol-plasticized films and PEG-plasticized films having the least absorption. We concluded that 3% w/v PEG film outperformed other PEG films and 3% w/v glycerol films. The cytotoxicity results showed that all films had a cell viability above the threshold of 75% and hence food-safe.
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Researchers developed a gelatin-agar bioplastic film using glycerol as a plasticizer, finding that approximately 72% of the material degraded naturally within 18 days, with tensile strength up to 0.32 MPa and good water resistance, demonstrating potential as a biodegradable alternative to petroleum-based plastics.
Biodegradable Food Packaging Films Using a Combination of Hemicellulose and Cellulose Derivatives
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Researchers developed biodegradable food packaging films by combining hemicellulose with methylcellulose or carboxymethyl cellulose, testing how biobased plasticizers like glycerol and polyethylene glycol affected their properties. Films containing hemicellulose and methylcellulose showed the best oxygen and water vapor barrier performance, suggesting agricultural waste-derived biopolymers could serve as sustainable alternatives to conventional plastic packaging.
Does the Hydrogel: Oleogel Ratio Affect the Physicochemical Properties of Gelatin–Beeswax Bioplastic Films?
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This study found that varying the ratio of hydrogel to oleogel in gelatin-beeswax bioplastic films significantly affects their thickness, solubility, tensile strength, and water vapor transmission. The optimized formulations offer a biodegradable alternative to conventional plastic food packaging, which contributes to microplastic pollution as it degrades.
Does the Hydrogel: Oleogel Ratio Affect the Physicochemical Properties of Gelatin–Beeswax Bioplastic Films?
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This study found that varying the ratio of hydrogel to oleogel in gelatin-beeswax bioplastic films significantly affects their thickness, solubility, tensile strength, and water vapor transmission. The optimized formulations offer a biodegradable alternative to conventional plastic food packaging, which contributes to microplastic pollution as it degrades.
A Basic Characterisation Study of Bioplastics via Gelatinization of Corn Starch
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Researchers synthesized bioplastics from corn starch via gelatinization at varying starch-to-glycerol ratios, finding that all formulations produced polyester-like functional groups by FTIR and that glycerol content controlled mechanical flexibility, with higher glycerol ratios yielding more pliable materials.
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When a large batch of papers lands in the Atlas, we read through it and send a short write-up of what stood out.