Bio‐based nanocomposites composed of photo‐cured epoxidized soybean oil and supramolecular hydroxystearic acid nanofibers

A mixture of epoxidized soybean oil (ESO), (R)-12-hydroxystrearic acid (HSA) and a photoinitiator for cationic polymerization in the ESO/HSA weight ratio 10/1 was heated to 100 °C and gradually cooled to room temperature to give bio-based gelatinous material. The photo-curing of the gel afforded a nanocomposite composed of crosslinked ESO and supramolecular HSA nanofibers. The transmission electron microscopy observation of the photo-cured ESO/HSA revealed that dendritic clusters of HSA nanofibers are formed in the crosslinked ESO matrix. In the differential scanning calorimetry chart of the ESO/HSA, a thermal transition from the mesophase composed of supramolecular nanofibers to isotropic state was observed at 67 °C (ΔH = 22.6 J/g-HSA), while the T m of crystalline HSA is 77.7 °C (ΔH m = 159 J/g-HSA). Tensile strength at 20 °C of the ESO-HSA was ∼80% higher than that of photo-cured ESO without HSA.

[1]  R. Narayan,et al.  Biocomposites synthesized from chemically modified soy oil and biofibers , 2006 .

[2]  F. E. Barton,et al.  "Green" composites from renewable resources: preparation of epoxidized soybean oil and flax fiber composites. , 2006, Journal of agricultural and food chemistry.

[3]  Soo-Jin Park,et al.  Synthesis and Thermal Properties of Epoxidized Vegetable Oil , 2004 .

[4]  M. Misra,et al.  Sustainable Bio-Composites from Renewable Resources: Opportunities and Challenges in the Green Materials World , 2002, Renewable Energy.

[5]  M. Misra,et al.  Biofibres, biodegradable polymers and biocomposites: An overview , 2000 .

[6]  J. Jog,et al.  Natural fiber polymer composites: A review , 1999 .

[7]  A. Błędzki,et al.  Composites reinforced with cellulose based fibres , 1999 .

[8]  K. Hanabusa,et al.  Easy preparation and useful character of organogel electrolytes based on low molecular weight gelator , 1999 .

[9]  R. Mülhaupt,et al.  Polyester networks based upon epoxidized and maleinated natural oils , 1997 .

[10]  B. Dahlke,et al.  Polyhydroxy fatty acids and their derivatives from plant oils , 1995 .

[11]  T. Tamura,et al.  Effect of alkali metal ions on gel formation in the 12-hydroxystearic acid/soybean oil system , 1994 .

[12]  P. Terech,et al.  Magnetic orientational effects during the aggregation kinetics of a steroid/cyclohexane gelling system , 1988 .

[13]  P. Terech Kinetics of aggregation in a steroid derivative/cyclohexane gelifying system , 1985 .

[14]  Tomoko Mori,et al.  Chiral Mesophases of 12-Hydroxyoctadecanoic Acid in Jelly and in the Solid State. I. A New Type of Lyotropic Mesophase in Jelly with Organic Solvents , 1980 .

[15]  Tomoko Mori,et al.  New type of twisted mesophase in jellies and solid films of chiral 12-hydroxyoctadecanoic acid , 1979, Nature.

[16]  K. Sakamoto,et al.  Liquid crystals composed of N-acylamino acids. I. Circular dichroism and selective light transmission in cholesteric liquid crystals composed of N-acylamino acids and organic solvents , 1978 .

[17]  D. Swern,et al.  Hydroxylation of Monounsaturated Fatty Materials with Hydrogen Peroxide , 1945 .

[18]  J. K. Wolfe,et al.  1,2,3,4-Dibenzylidene-D-sorbitol , 1942 .