Effects of Isosorbide Incorporation into Flexible Polyurethane Foams: Reversible Urethane Linkages and Antioxidant Activity

Isosorbide (ISB), a nontoxic bio-based bicyclic diol composed from two fuzed furans, was incorporated into the preparation of flexible polyurethane foams (FPUFs) for use as a cell opener and to impart antioxidant properties to the resulting foam. A novel method for cell opening was designed based on the anticipated reversibility of the urethane linkages formed by ISB with isocyanate. FPUFs containing various amounts of ISB (up to 5 wt%) were successfully prepared without any noticeable deterioration in the appearance and physical properties of the resulting foams. The air permeability of these resulting FPUFs was increased and this could be further improved by thermal treatment at 160 °C. The urethane units based on ISB enabled cell window opening, as anticipated, through the reversible urethane linkage. The ISB-containing FPUFs also demonstrated better antioxidant activity by impeding discoloration. Thus, ISB, a nontoxic, bio-based diol, can be a valuable raw material (or additive) for eco-friendly FPUFs without seriously compromising the physical properties of these FPUFs.

Vegetable Tannin as a Sustainable UV Stabilizer for Polyurethane Foams

A vegetable tannin, a flavonoid-type natural polyphenolic compound, was used to promote the stabilization of polyurethane foams against UV radiation. Several polyurethane foams were synthesized by using an isocyanate, and a mixture of ethoxylated cocoalkyl amine and vegetable tannin. The content of vegetable tannin was varied from 0 to 40 wt %. The effects of tannin and water (used as a blowing agent) on the foaming kinetics and cellular morphology of foams were investigated. Samples were subjected to accelerated weathering under UV radiation for 3 to 24 h, and FTIR and DMA analyses were conducted to assess the performance change. The former analysis revealed a strong inhibiting effect of tannin on urethane linkage degradation during the UV treatment. The mechanical properties were significantly affected by the addition of tannin. The capability of the foams to withstand UV radiation was dependent on the amount of tannin. At tannin contents higher than 20%, the decrease in mechanical properties under UV irradiation was almost avoided.

Study on the effect of silica–graphite filler on the rheometric, mechanical, and abrasion loss properties of styrene–butadiene rubber vulcanizates

Silica–graphite filler was prepared via two-step grafting procedure by grafting silica particles onto the expanded graphite. In the first step, isocyanatopropyltriethoxysilane was chemically introduced onto the silica aggregates, which was followed by grafting onto the expanded graphite via urethane linkage in the second step. Successful grafting of silica aggregates onto the graphite was corroborated using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The presence of a thin graphene layer on silica aggregates corroborated using transmission electron microscopy confirmed the grafting of silica aggregates onto the graphite surface. Styrene–butadiene rubber (SBR) composites with various silica–graphite loadings were prepared by melt processing technique to generate pristine silica and silica–graphite-filled elastomeric composites. Rheometric cure studies revealed that the torque difference (Δ S) increased with pristine silica loading, when compared to the unfilled SBR system, and this effect is more pronounced on loading silica–graphite filler. Improvements in mechanical properties such as modulus and tensile strength were observed with increasing loading of silica particles and this effect is more pronounced on loading silica–graphite fillers, indicating that this is due to the rise in the elastomer–filler interactions in the silica–graphite-loaded SBR systems. This fact was further corroborated using bound rubber content and equilibrium swelling ratios of the unvulcanized and vulcanized SBR composites.

Preparation and Characterization of Polyurethane Nanocomposites Using Vietnamese Montmorillonite Modified by Polyol Surfactants

This study focuses on the preparation of thermoplastic polyurethane (TPU) nanocomposite using Vietnamese montmorillonite (MMT) as the reinforced phase. The MMT was previously modified by intercalating polyethylene oxide (PEO) and polyvinyl alcohol (PVA) molecules between the clay layers. X-ray diffraction (XRD) results of organoclays revealed that galleries of MMT were increased to 18.2 Å and 27 Å after their intercalation with PEO and PVA, respectively. Thermoplastic polyurethane (TPU) nanocomposites composed of 1, 3, 5, and 7%wt organoclays were synthesized. The result of XRD and transmission electron microscopic (TEM) analyses implied that the PEO modified MMT was well dispersed, at 3%wt, in polyurethane matrix. Fourier Transform Infrared Spectroscopic (FTIR) has confirmed this result by showing the hydrogenous interaction between the urethane linkage and OH group on the surface of silicate layer. Thermogravimetric (TG) showed that the organoclay samples also presented improved thermal stabilities. In addition, the effects of the organoclays on mechanical performance and water absorption of the PU nanocomposite were also investigated.