Fabrication of Woven Jute Fiber Epoxy Bio-Composites through the Epoxy/Thiol-Ene Photopolymerization Technique.

An eco-friendly epoxy/thiol-ene photopolymerization (ETEP) process was employed to prepare epoxy bio-composites using a commercial biobased epoxy resin and a woven jute fabric as reinforcement. In this process the components of the thiol-ene system, an allyl-functionalized ditertiary amine curing agent, a multifunctional thiol and a radical photoinitiator, were added to the epoxy resin to produce a polyether-polythioether crosslinked co-network. Moreover, the jute fibers were functionalized with thiol groups using the 3-mercaptopropyl (trimethoxysilane) with the purpose of creating a chemically bonded polymeric matrix/fiber system. The obtained bio-composites prepared with the thiol-functionalized cellulose fibers exhibited an increase up to 52% and 40% in flexural modulus and strength with respect to the non-functionalized counterparts. Under the three-point bending loadings, the composites displayed higher deformation at break and toughness due to the presence of polythioethers in the co-network. The prepared bio-composites developed in this work are excellent candidates to extend the use of cellulose fibers for structural applications.

Synthesis of glycerol-derived diallyl spiroorthocarbonates and the study of their antishrinking properties in acrylic dental resins.

In this work was evaluated the efficiency of an antishrinkage additive in a dental resin. This additive was a mixture 1:1 of five and six-membered ring spiroorthocarbonates functionalized with allylic groups (SOC DA). The aim of this study was to reduce the shrinkage of a typical dental resin composed of a blend of the dimethacrylates, Glycerolate bisphenol A dimethacrylate (Bis-GMA)/2-[(3,5,5-trimethyl-6-[2-(2-methyl prop-2-enoyloxy) ethoxycarbonylamino] hexyl) carbamoyloxy] ethyl, 2-methyl prop-2-enoate, (UDMA)/triethyleneglycol dimethacrylate (TEGDMA) in a 50:30.20 molar ratio, and silicon dioxide as filler. SOC DA was added at 5, 10 and 20 mol% to the already mentioned formulation. It was found that the addition of 20 mol% of SOC DA decreased 53 % the shrinkage of the cured composite material, in comparison with a formulation where it was not added the antishrinkage additive. Besides, the kinetics of photopolymerization determined by Real-Time infrared spectroscopy, demonstrated that the addition of increasing concentration of SOC DA improved the conversion of double bonds of dimethacrylates. Additionally, the presence of SOC DA at 10 % mol, helped to increase the flexural strength and the compressive strength of the composite, as a consequence of the augment of the crosslink density, induced by the ring opening polymerization of SOC DA.