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By increasing the environmental concerns and depletion of petroleum resources, bio-based resins have gained interest. Recently, lignin, vanillin (4-hydroxy-3-methoxybenzaldehyde), and divanillin (6,6′-dihydroxy-5,5′-dimethoxybiphenyl-3,3′-dicarbaldehyde)-based resins have attracted attention due to the low cost, environmental benefits, good thermal stability, excellent mechanical properties, and suitability for high-performance natural fiber composite applications. This review highlights the recent use of lignin, vanillin, and divanillin-based resins with natural fiber composites and their synthesized processes. Finally, discussions are made on the curing kinetics, mechanical properties, flame retardancy, and bio-based resins’ adhesion property.

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Recycled bamboo fiber-reinforced chemically functionalized ethylene propylene rubber (R-BMBF/CF-EPR) composites have been developed by extrusion and injection molding by Palsule process without any fiber treatment and without compatibilizer. Scanning electron microscopy (SEM) shows good R-BMBF/CF-EPR interfacial adhesion in the composites, and Fourier transform infrared (FTIR) confirms that esterification and the hydrogen bonding between functional groups of CF-EPR and of R-BMBF impart this interfacial adhesion. Mechanical, dynamic mechanical, and thermal properties and the effect of water absorption on tensile properties of the composites have been evaluated. Tensile properties of the 15/85, 25/75, and 35/65 R-BMBF/CF-EPR composites are higher than those of CF-EPR and increase with increasing R-BMBF in the composites. Storage modulus and loss modulus of the composites increase with increasing fiber contents in them but decrease with increasing temperature. Water-absorbed wet composites show thickness swelling and reduced tensile properties relative to the respective dry composites but higher tensile properties than the dry CF-EPR. Thermal stability and degradation of the composites is also reported.

The synthesis, X-ray structure and role of intermolecular interactions have been studied in case of 1,3-diphenyl-urea, owing to its medicinal importance. The compound crystallizes in orthorhombic crystal system (space group, Pna2 1) with unit cell parameters, a = 9⋅ ⋅118(3), b = 10⋅ ⋅558(2), c = 11⋅ ⋅780(3) Å and Z = 4. The structure has been solved by direct methods and refined to a final R-value of 0⋅ ⋅0316. The oxygen atom of the carbonyl group is responsible for the existence of two N-H…O intermolecular interactions.