Woven and nonwoven flax fiber reinforced poly lactic acid (PLA) biocomposites were prepared with amphiphilic additives as accelerator for biodegradation. The prepared composites were buried in farmland soil for biodegradability studies. Loss in weight of the biodegraded composite samples was determined at different time intervals. The surface morphology of the biodegraded composites was studied with scanning electron microscope (SEM). Results indicated that in presence of mandelic acid, the composites showed accelerated biodegradation with 20–25% loss in weight after 50–60 days. On the other hand, in presence of dicumyl peroxide (as additive), biodegradation of the composites was relatively slow as confirmed by only 5–10% loss in weight even after 80–90 days. This was further confirmed by surface morphology of the biodegraded composites. We have attempted to show that depending on the end uses, we can add different amphiphilic additives for delayed or accelerated biodegradability. This work gives us the idea of biodegradation of materials from natural fiber reinforced PLA composites when discarded carelessly in the environment instead of proper waste disposal site

Biodegradable soy protein isolate (SPI), containing 2,2-diphenyl-2-hydroxyethanoic acid, films (SB) were successfully prepared with bis-(2-hydroxyethyl)sulfide as a plasticizer by compression molding at 155 degrees C and 15 MPa. By immersing the SB in distilled water for 26 h, we prepared the films (coded as SB-WM) having good water resistance. The films were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, dynamic mechanical thermal analysis, and tensile testing to evaluate their structure and properties. Moreover, the surface of the SB-WM films was analyzed by X-ray photoelectron spectroscopy and contact angle measurement. SB-WM films exhibited significantly higher contact angle than SB. The results revealed that a lotus-like nanoscale structure was created in SB-WM films, with increased hydrophobicity, through the process of the solvent-induced microphase separation during the immersion in water. More stable compound diphenylhydroxymethane could form from 2,2-diphenyl-2-hydroxyethanoic acid of SB in water, leading to the hydrophobicity of the SB-WM materials. A "green" and easy method for fabricating hydrophobic materials from soy protein has been provided in this work.

Thiodiglycol (TDG) is a relatively nontoxic compound from organic wastes. By using TDG as a plasticizer with weights from 2.5 to 40%, we prepared soy protein isolate (SPI) films by a compression-molding technique at 140 C and 15 MPa. The TDG-plasticized films (SPI-TDG films) were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, dynamic mechanical thermal analysis, thermogravimetric analysis, optical transmittance, and water uptake experiments. The SPI-TDG film plasticized with 25% TDG exhibited good mechanical properties, such as a tensile strength and modulus of 20.3 and 582 MPa, respectively, whereas the SPI-glycerol film with 25% glycerol had a tensile strength and modulus of 16.2 and 436 MPa, respectively. The results from the thermogravimetric analysis and water uptake experiments indicated that the thermal stability and water resistance of the TDG-plasticized SPI materials were higher than that of the glycerol-plasticized one. The improvements in the mechanical properties, water resistance, and thermal stability of the SPI-TDG films could be attributed to the strong intermolecular hydrogen bonding between soy protein and TDG and the presence of fewer hydroxyl groups in TDG, as compared structurally with glycerol. This study provided a new plasticizer for the preparation of soy protein materials.

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