Ionic conductivity enhancement of PVA: carboxymethyl cellulose poly-blend electrolyte films through the doping of NaI salt

Cellulose - In this paper, we report the effect of doping sodium iodide (NaI) salt into a polymer blend matrix of sodium carboxymethyl cellulose (NaCMC) and poly(vinyl alcohol) (PVA). Solution...     

The Structures and Physicochemical Properties of Mixtures of Water-Soluble Polymers

Because data on structure, component interaction, physical properties, and compatibility of polymer blends containing native polysaccharides is very sparse, we have used optical and electron microscopy, X-ray diffraction, IR spectroscopy, sorption capacity methods, and estimation of thermodynamic data to investigate the structural, physicochemical, and physicomechanical properties of mixtures of carboxymethylcellulose with poly(vinyl alcohol) and of mixtures of chitosan with poly(vinyl alcohol), to discover relationships between the structures of the systems and their physicochemical characteristics and other properties, to determine the compatibility of components, and to discover methods and conditions for their synthesis. It was found that for some component ratios in these systems there is some interaction and some compatibility, with the result that the structures of the blends are less heterogeneous than those of the individual components. One effect of this is that the physicomechanical properties of the blends can be superior to those of the individual components, particularly for carboxymethylcellulose–poly(vinyl alcohol) mixtures.Presented at: International Symposium on Separation and Characterization of Natural and Synthetic Macromolecules, Amsterdam, The Netherlands, February 5–7, 2003     

Viscoelasticity and surface properties of blends of aqueous solutions of polyvinyl alcohol and carboxymethyl cellulose

Rheological properties of aqueous solutions of carboxymethyl cellulose, polyvinyl alcohol, and of their blends prepared under various conditions (temperature, concentration, time) were studied by viscometry and of ball indenter penetration.     

Thermorheological studies on polymeric blends

Two petroleum-derived aromatic hydrocarbon resins (HRs) were blended (1:1) with expanded polystyrene (EPS) waste and small amounts (up to 10 mass%) of poly(vinyl chloride) (PVC) to increase both the lustrous carbon (LC) yield and softening point of the blends without any deterioration of their rheological characteristics. The blends were prepared and tested for LC content, softening points, shear stress and apparent viscosity to check their applicability as LC precursors under industrial conditions. The properties of polystyrene compositions with bitumen fractions depend primarily on composition and viscosity of oil fraction. Additional modification by poly(vinyl chloride) improves the blends’ properties, like bright coal content, softening point and viscosity, and opens new possibilities of plastics’ wastes utilization.     

氯化聚氯乙烯／环氧树脂共混体的流变性质及形态

氯化聚氯乙烯(CPVC)具有优良的物理性能。但须严格控制加工温度,加工熔体粘度较大。近年,作者曾对CPVC与氯化聚乙烯(CPE)和丙烯酸酯共聚物(ACR)共混体的流变性质进行了研究。本文首次研究CPVC与环氧树脂(EP)共混体的流变性质与形态。     

Influence of fibrous and solid fillers on the rheological and surface properties of polymer compositions

The influence of fibrous and solid granulated fillers on the rheological and surface properties of polymer compositions on the basis of poly(vinyl alcohol) and carboxymethyl cellulose is demonstrated. The effect of the concentration of initial polymer solutions and the time of complex formation on the properties of polymer complexes upon the addition of various fillers is revealed.     

pH effects on the complexation, miscibility and radiation-induced crosslinking in poly(acrylic acid)-poly(vinyl alcohol) blends

The effect of pH on the complexation of poly(acrylic acid) with poly(vinyl alcohol) in aqueous solution, the miscibility of these polymers in the solid state and the possibility for crosslinking the blends using gamma radiation has been studied. It is demonstrated that the complexation ability of poly(vinyl alcohol) with respect to poly(acrylic acid) is relatively low in comparison with some other synthetic non-ionic polymers. The precipitation of interpolymer complexes was observed below the critical pH of complexation (pH(crit1)), which characterizes the transition between a compact hydrophobic polycomplex and an extended hydrophilic interpolymer associate. Films prepared by casting from aqueous solutions at different pH values exhibited a transition from miscibility to immiscibility at a certain critical pH, pH(crit2), above which hydrogen bonding is prevented. It is shown here that gamma radiation crosslinking of solid blends is efficient and only results in the formation of hydrogel films for blends prepared between pH(crit1) and pH(crit2). The yield of the gel fraction and the swelling properties of the films depended on the absorbed radiation dose and the polymer ratio. [Diagram: see text] SEM image of an equimolar PAA-PVA blend cast from a pH 4.6 solution.     

Properties of aqueous solutions of blends of polyvinyl alcohol with carboxymethyl cellulose ionized to various extents

Russian Journal of Applied Chemistry - The rheological properties of dilute and moderately concentrated aqueous solutions of blends of polyvinyl alcohol with carboxymethyl cellulose ionized to...     

Preparation and Characterization of Blend Films of Poly(Vinyl Alcohol) and Sodium Alginate

Blend films of poly(vinyl alcohol) (PVA) and sodium alginate (NaAlg) were prepared by casting from aqueous solutions. This blend films were characterized by tensile strength test, Fourier transform infrared spectroscopy (FT‐IR), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The miscibility in the blends of PVA and NaAlg was established on the basis of the thermal analysis results. DSC showed that the blends possessed single, composition‐dependent glass transition temperatures (T_gs), indicating that the blends are miscible. FT‐IR studies indicate that there is the intermolecular hydrogen bonding interactions, i.e. –OH…^?OOC– in PVA/NaAlg blends. The blend films also exhibited the higher thermal stability and their mechanical properties improved compared to those of homopolymers.     

Biodegradable systems: Thermodynamics, rheological properties, and biocorrosion

Systems based on starch and chitosan blends with synthetic polymers and cellulose derivatives (poly(ethylene oxide) and methyl cellulose of various molecular masses, PA, and ethylene-vinyl acetate copolymers containing different amounts of vinyl acetate groups) have been studied. The thermodynamic characteristics of the formation of blends have been determined. The rheological properties characterizing formation of blends from melts have been investigated. The biocorrosion ability of the blends after their use has been estimated by various methods. The concentration dependences of the thermodynamic functions of mixing of components (change in the Gibbs energy, enthalpy, and entropy) change sign in a wide composition range, indicating the complexity of mixing of rigid-chain natural polysaccharides with synthetic polymers. The rheological study of blends in which starch or chitosan plays the role of a biodegradation modifier shows that they are non-Newtonian fluids. The absolute values of viscosity and the activation parameters of melts increase with the content of polysaccharide in the system. The values of viscosity correspond to those typical for commercially processable polymers. The blends under study are biodegradable in a wet and water-soil medium with the content of the natural component being in the range 15–30 wt %.     

Morphology,mechanical, and water transport properties of melt blended EVOH/PVOH films

Herein, we report for the first time the successful preparation of ethylene–vinyl alcohol (EVOH)/poly(vinyl alcohol) (PVOH) blends by a melt blending process for PVOH volume content ranging from 0 to 30%. Thermal stability up to 270 °C was maintained for all blends. The blends morphology consisted in spherical low size PVOH domains homogeneously dispersed in the EVOH matrix with good interfacial properties. An increase of the mean size of the PVOH domains (from 0.3 to 1.2 μm) and of the size distribution was evidenced as the PVOH content increased. The contribution of each phase to the water sorption and diffusion was clearly demonstrated. The impact of water uptake was investigated on the chains mobility by using Gordon–Taylor law and on the mechanical properties of the blends with respect to the reference polymers. It was pointed out that the reinforcing effect of PVOH phase decreased as the water activity increased. However, a significant elongation at break was maintained, underlining the major role played by the EVOH continuous phase at high water activity. Finally, it was shown that adding PVOH to EVOH up to 15 vol % allowed strengthening the material at low water activity and keeping interesting elongation at break and barrier properties at high water activity. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 838–850     

Effects of Electron Beam Irradiation on the Structural Properties of PVA/PAM/CMC Ternary Polymer Blends

Ternary miscible blends based on various ratios of poly(vinyl alcohol) (PVA), poly(acrylamide) (PAM) and carboxymethyl cellulose (CMC) were prepared by solution casting in the form of thin films. The structure‐property behavior of the ternary PVA/PAM/CMC blends, before and after they had been exposed to various doses of electron beam irradiation, was investigated by FT‐IR spectroscopy, SEM, XRD and stress‐strain curves. The visual observation showed that the cast films of the individual polymers PVA, PAM, and CMC and their blends over a wide range of composition are clear and transparent indicating the miscibility of PVA/PAM/CMC ternary blends. The FT‐IR analysis of pure polymers or their ternary blends before or after electron beam irradiation proved the formation of hydrogen bonding. In addition, it was found that the intensity of the different absorption bands depends on the ratio of PAM and CMC in the ternary blend. The XRD patterns showed that the peak position for the ternary blends decreases with increasing the ratio of CMC in the blend. However, the peak position for the ternary blend based on equal ratios of pure polymers was not affected by blending and was found in the same position as in the XRD pattern of pure PVA. The SEM micrographs give support to the visual observation indicating the complete miscibility of PVA/PAM/CMC ternary blends. The improvement in morphology leads to improvement in the tensile mechanical properties of the ternary polymer blends.     

Polypeptide-synthetic polymer hybrids, 1. Miscibility of poly(vinyl alcohol) with poly(sodium α,β-D,L-aspartate)

The present paper describes materials of polypeptide-commodity polymer hybrids from poly(vinyl alcohol) (PVA) and poly(sodium α,β-D ,L -aspartate) ( 1 ). Miscible blend films of polypeptide 1 and PVA were prepared by the solvent-cast method from a homogeneous aqueous solution. Differential scanning calorimetry. Fourier transform infrared, and scanning electron microscopy combined with energy dispersive X-ray spectroscopy (EDX) were used to investigate the blends. It was revealed that 1 and PVA are miscible in a wide range of compositions.     

Effect of temperature on the intrinsic viscosity of poly(ethylene glycol)/poly(vinyl pyrrolidone) blends in aqueous solutions

In this work the intrinsic viscosity of poly(ethylene glycol)/poly(vinyl pyrrolidone) blends in aqueous solutions were measured at 283.1–313.1 K. The expansion factor of polymer chain was calculated by use of the intrinsic viscosities data. The thermodynamic parameters of polymer solution (the entropy of dilution parameter, the heat of dilution parameter, theta temperature, polymer–solvent interaction parameter and second osmotic virial coefficient) were evaluated by temperature dependence of polymer chain expansion factor. The obtained thermodynamic parameters indicate that quality of water was decreased for solutions of poly(ethylene oxide), poly(vinyl pyrrolidone) and poly(ethylene oxide)/poly(vinyl pyrrolidone) blends by increasing temperature. Compatibility of poly(ethylene oxide)/poly(vinyl pyrrolidone) blends were explained in terms of difference between experimental and ideal intrinsic viscosity and solvent–polymer interaction parameter. The results indicate that the poly(ethylene glycol)/poly(vinyl pyrrolidone) blends were incompatible.     

Synthesis,UV-curing behavior and surface properties of fluorine-containing vinyl ether polymers

Five fluorine-containing vinyl ether monomers were prepared by the reaction between 2-vinyloxy ethanol, a fluorinated alcohol and hexafluorobenzene in the presence of sodium hydride in dimethylformamide. Two representative properties of these monomers, UV-curing behavior initiated by a cationic photo-initiator PAG 201 and surface free energy of coating films, were investigated. Photo-polymerization proceeded both rapidly and completely with a high double-bond conversion （〉 90%） and a fast curing rate （maximum curing time 〈 21 s） for three monomers. The surface energies of the monomers and the resulting polymer films were then investigated. The minimum surface free energy of the UV-cured homopolymer films reaches 7.1 mJ/m2. X-ray photoelectron spectroscopy data show that the low surthce tension is influenced by fluorine content in the soft segments and fluorinated chains＇ migration to the surface. The five monomers exhibit low viscosity, low surface energy, good thermal stability and good photo-polymerization properties, which make them great candidates for UV coating and photoresist applications.     

Acrylic Terpolymer-Based Blends with Improved Properties

Blending of acrylic terpolymer (AT) with vinyl acetate-vinyl chloride (VAc-VC) copolymer, polyvinyl alcohol (PVA) polymer, and polyvinyl acetate (PVAc) polymer, respectively, resulted in sealant compositions with improved properties and enhanced outdoor weathering resistance. The morphology of these blends was studied by SEM, energy-dispersive x-ray analysis (EDXA), and DSC. The blends are heterogeneous and consist of a continuous phase which is either pure or mixed AT and a particulate phase having the morphology of the added component. The particulate phase of AT and AT-(VAc-VC) copolymer blends contains mixed AT, whereas that of AT-PVA and AT-PVAc does not. The AT-based blends have generally improved mechanical properties (e.g., ultimate tensile strength, adhesive strength). The improvement in mechanical properties is particularly strong in mixtures of AT with (VAc-VC) copolymer, probably because the added component has greater specific interaction capabilities with AT than the polymers incorporated in the other blends. Whereas the unblended AT has very low outdoor durability, the AT-based blends display enhanced resistance to weathering, as evidenced by substantially higher ultimate tensile strength of weathered specimens than those of the controls (unweathered).     

Preparation and characterization of ternary composite films of polyvinyl alcohol/sodium alginate/TiO<Subscript>2</Subscript>

Nano-TiO₂ with anionic surface active agent sodium dodecylsulfate (SDS) modified, the poly(vinyl alcohol)/sodium alginate/TiO₂ composite films were prepared by method of solution blending representing. The structure of the films was analyzed by XRD and SEM. In addition, air permeability rate, swelling ratio, light transmittance, mechanical properties, and antibacterial properties were tested. The results showed that in compound membrane there was a strong force between poly(vinyl alcohol)/sodium alginate and TiO₂ particles, indicating that there was good compatibility between the sodium alginate and the poly(vinyl alcohol). The mixed membranes were of good water resistance, tensile strength, and closure. When the titanium dioxide content increased appropriately, they had very good mechanical properties. In addition, the antibacterial properties of composite membrane gradually increased with the increase in the TiO₂content.     

Oxygen permeability in blends of a vinyl alcohol/ethylene copolymer and a metallocenic ethylene/1‐octene copolymer

This work describes the preparation, characterization, and evaluation of the oxygen permeability of blends based on a polyolefin synthesized with a metallocene catalyst (ethylene/1‐octene copolymer) and a vinyl alcohol/ethylene copolymer in an attempt to establish the corresponding relationships between the composition, morphology, and transport properties to design materials with optimized and enhanced agricultural and food packaging performances. Moreover, microhardness measurements have been used to analyze the mechanical response of these blends and to obtain information about the dispersion of the two immiscible components within the blends. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3766–3774, 2004     

Mechanical, morphological and biodegradation studies of microwave processed nanostructured blends of some bio-based oil epoxies with poly (vinyl alcohol)

Bioresource based blends exploit the synergy between polymers derived from renewable resource and commercial polymers to obtain desirable physical, mechanical, and biodegradable properties. With the aim to develop a sustainable resource based biodegradable mulch films, nanostructured blends of epoxies of linseed oil (LOE) and dehydrated castor oil (DCOE) with poly (vinyl alcohol) (PVA) were prepared in the weight ratios of 20/80, 50/50 and 80/20. Microwave-assisted blending was used for the synthesis of DCOE/LOE blends with PVA and the results were compared with conventional solution blending using FT-IR, TGA-DTA and optical measurements. The results revealed that microwave-assisted blending proved to be an efficient method for the formation of compatible blends in a short span of time as compared to conventional solution blending. Transmission electron microscopy (TEM) analysis of DCOE/PVA and LOE/PVA blends synthesized by microwave-assisted method confirmed the formation of a nanostructured blend. Scanning electron microscopy (SEM), respirometry and mechanical measurements were carried out to compare the morphology, biodegradability, and the mechanical strength of DCOE/PVA and LOE/PVA blends. It was observed that DCOE/PVA blends exhibited higher biodegradability, better mechanical properties, and lower moisture absorption characteristics as compared to LOE/PVA blends. The mechanical strength, moisture absorption, and biodegradability of these blends were also compared with blends of other bioresource based polymers such as sugarcane bagasse (SCB), waste gelation (WG), apple peal (AP), and starch/glycerol with PVA, as available from the cited literature in the text.     

Synthesis and characterization of a flame retardant hyperbranched polyether

<正>A brominated hyperbranched polyether has been synthesized from cyanuric chloride and sodium salt of tetrabromobisphenol-A by an A_2+B_3 approach.The synthesized polyether was characterized by ~1H-NMR,~(13)C-NMR,UV, FTIR spectroscopy and X-ray diffraction studies,measurements of solution viscosity,molecular weight and solubility and elemental and thermogravimetric analyses.The flame retardancy of the synthesized polyether and its blends with commercially available plasticized poly(vinyl chloride)(PVC) and low density polyethylene(LDPE) was investigated by measurements of limiting oxygen index(LOI) value and thermogravimetric analysis.The properties are compared with a non-halogenated similar type of bisphenol-A based aromatic polyether after blending at different dose levels with the same base polymers.The LOI values of these blends indicated that these hyperbranched polyethers acted as flame retardant additives,and antimony trioxide had prominent synergistic effect with the bromo hyperbranched polyether for the above base polymers,and an increment of 4 to 6 units in LOI values was observed.