Polyvinyl Acetate and Vinyl Acetate-Ethylene Hybrid Adhesive: Synthesis, Characterization, and Properties

The goal is to develop a hybrid IPN network of polyvinyl acetate (PVAc) and ethylene-vinyl acetate (VAE). In this research work, the vinyl acetate (VAc)/ VAE hybrid emulsion and polyvinyl acetate emulsion (PVAc) were effectively synthesized. Emulsions with various characteristics have been developed by adjusting the weight ratios between the vinyl acetate monomer and the VAE component. The impacts on the mechanical, thermal, and physical properties of the films were investigated using tests for pencil hardness, tensile shear strength, pH, contact angle measurement, differential scanning calorimetry (DSC), and viscosity. When 5.0 weight percent VAE was added, the tensile shear strength in dry conditions decreased by 18.75% after a 24-hour bonding period, the heat resistance decreased by 26.29% (as per WATT 91) and the tensile shear strength decreased by approximately 36.52% in wet conditions (per EN 204). The pristine sample’s results were also confirmed by the contact angle test. The interpenetrating network (IPN) formation in hybrid PVAc emulsion as primary bonds does not directly attach to PVAc and VAE chains. The addition of VAE reduced the mechanical properties (at dry conditions) and heat resistance as per WATT 91. Contact angle analysis demonstrated that PVAc adhesives containing VAE had increased water resistance when compared to conventional PVA stabilised PVAc homopolymer-based adhesives. When compared to virgin PVAc Homo, the water resistance of the PVAc emulsion polymerization was enhanced by the addition of VAE.

Effects of Nano-Filler on the Thermal and Fire-Resistant Properties of Ethylene-Vinyl Acetate Copolymer

Sepiolite （S9, B10, B20, B40） and boehmite have been added to an intumecent flame retardant （IFR） system to produce the halogen-free and fire-resistant ethylene-vinyl acetate copolymer （EVM） rubber. The rubber contains ammonium polyphosphate （APP） as acid source, double pentaerythritol （D-PER） as carbon source and melamine （MN） as gas source. The effects of nano-filler sepiolite and boehmite on the fire-resistant property of EVM rubber based on IFR system were investigated. The test results show that the system with nano-filler of sepiolite B10 has the best fire-resistant property. The process of smoke emission and thermal decomposition, the element composition of char surface and the micro morphology of intumecent char layer of the EVM IFR system with nano-filler were also studied by NBS chamber, thermogravimetric （TG） analysis, X- ray photoelectron spectroscopy （XPS） and scanning electron microscope （SEM）.

NON-ISOTHERMAL CRYSTALLIZATION OF ETHYLENE-VINYL ACETATE COPOLYMER CONTAINING A HIGH WEIGHT FRACTION OF GRAPHENE NANOSHEETS AND CARBON NANOTUBES

The effect of the different geometrical dimensionality of two dimensional graphene nanosheets （2D GNSs） and one dimensional carbon nanotubes （1D CNTs） on the non-isothermal crystallization of an ethylene-vinyl acetate （EVA） copolymer at high loading （5 wt%） was studied. Transmission electron microscopy indicated a homogeneous dispersion of GNSs and CNTs in EVA obtained by a solution dispersion process. Fourier-transform infrared spectroscopy and differential scanning calorimetry measurements showed that 1D CNTs and 2D GNSs acted as effective nucleating agents, with a noticeably increased onset crystallization temperature of EVA. A high weight fraction of nano-fillers slowed the overall crystallization rate of composites. At the same crystallization temperatute, the crystallization behavior of GNS/EVA composites was slowed compared to that of the CNT/EVA ones owing to larger nucleus barrier and activation energy of diffusion. Dynamic mechanical relaxation and rheology behavior of CNT/EVA and GNS/EVA composites demonstrated that the planar structure of the GNSs had an intensively negative effect on EVA chain mobility due to interactions between nano- fillers and polymer chains, as well as spatial restriction.

Influence of Curing Condition on the Adhesive Strength of EVA Modified Mortar to Tile

The reducing water effectiveness of EVA latex and powder was observed. Adhesive strength of EVA modified mortar to tile under different curing condition was studied. And the adhesive strengths of mortars modified by EVA latex and by EVA powder were compared. The results show that the reducing water effectiveness is improved by 36.12% and 21.55%, respectively, when the content of EVA latex and powder are 8% and 4%. EVA latex and powder can improve the adhesive strength of modified mortar to tile under the standard curing, high temperature curing, and freeze-thaw circle curing. EVA latex can improve the water resistance obviously, besides improve the adhesive strengths of standard curing and high temperature curing, comparing with EVA powder.

Effect of Different Organic Modifiers on the Tensile Properties of PVC/EVA/Montmorillonite Composites

Poly (vinyl chloride)/ethylene-vinyl acetate/montmorillonite (PVC/EVA/OMMT) composites were prepared by melt blending method. Two kinds of montmorillonites were organically modified by trimethyloctadecyl ammonium and dimethyl bis (hydrogenated tallow) ammonium, respectively. The morphology and tensile properties of the resultant composites were discussed in terms of the modifier type and OMMT content. The PVC/EVA/OMMT composites have intercalated structure, which is independent of the polarity of the modifiers, while the tensile properties show strong dependence on the modifier type. The OMMT modified by polar modifier gives higher tensile ductile and strength of PVC/EVA/OMMT composites.

Preparation and Characterization of Flame Retardant and Low Smoke Releasing Oil-resistant EVA/NBR Blends

Nano-SiO2 and/or MoO3 were introduced to ethylene-vinyl acetate/nitrile butadiene rubber （EVA/NBR） blends containing magnesium hydroxide （MH） and red phosphorus （RP） to further improve the mechanical properties, oil resistance, smoke suppression and flame retardancy. The results indicated that the tensile strength and oil resistance were significantly improved by incorporating nano-SiO2. Smoke suppression tests for EVA/NBR blend samples showed that both nano-SiO2 and MoO3 can significantly reduce smoke release amount. The flammability characterization indicated that the blended sample with an LOI value of 33.0 could achieve V-0 level in the UL-94 test. Cone calorimetry test data showed the peak heat release rate was 67% lower than that for pure EVA/NBR. Thermal analysis showed that the presence of both nano-SiO2 and MoO3 was beneficial to promoting char formation of the EVA/NBR blends. Char residual analysis suggested that MoO3 aggregated in solid phase during combustion.

Supercritical Fluid Media in Challenges of Substance and Material Dispersion

The paper deals with the problem of material dispersion using supercritical fluid media. At the same time, emphasis is made on modifications(SAS, GAS, SEDS and ASES) of the supercritical fluid anti-solvent method of dispersion. The results of SAS method implementation for dispersion of pure polycarbonate and polycarbonate doped with "CdSe/CdS-core/shell" quantum dots(carried out in the pressure range of 8.0-25.0 MPa at temperatures of 313.15 K and 358.15 K) are submitted. The range of the operating parameters has been established through the example of pure polycarbonate dispersion, which provides the production of nanoparticles with the size range of 10-100 nm. Encapsulation of Cd Se/Cd S quantum dots into polycarbonate using the SAS method has no effect on optical properties of the encapsulated quantum dots. The results of paracetamol dispersion using the SEDS method are presented. The effect of operating conditions of the paracetamol dispersion process on morphology of the obtained product is described. Co-dispersion of ethylene–vinyl acetate copolymers and low-density polyethylene mixtures by SEDS method has been carried out under pressures of 8.0-25.0 MPa at temperatures of 313 K, 323 K, and 333 K. The comparison of melting and crystallization between the resulting copolymer mixtures and mixtures with the same composition obtained by mixing in the liquid melt, has shown that implementation of SEDS results in an increase of crystallinity degree of the polymer mixtures.