Bond Strength–Disbonding Behavior and Dimensional Stability of Walnut and Poplar Impregnated with Some Chemicals and Bonded with PVAc,VTKA and Urea Formaldehyde

The aim of this study, is to describe the effects of adhesives (PVAc-Desmodur VTKA and Urea formaldehyde) on wooden materials (walnut and poplar) cut tangentially and radially impregnated with Protim Solignum, CCA and Celcure AC 500 and exposed to: humid–water–heat resistance; heating; and cooling tests. All these tests show a decreased in bonding strength. The conclusion is that poplar wood cut tangentially and impregnated with CCA, bonded with D-VTKA adhesive can be used as a material in damp conditions where good bond strength is required.     

Evaluation of the Effect of Nanosilica on Thermal and Mechanical Properties of Metal–Metal and Metal–Glass Canola-Based Polyurethane/Nanosilica Adhesives

Nanocomposites with different concentration of nanofiller were prepared by adding nanosilica to the canola-based polyurethane matrix via in situ polymerization. The effect of nanosilica on the mechanical properties of adhesives was evaluated by tensile tests. Adhesive characteristics on metal–metal and metal–glass bondings were also evaluated by lap shear strength tests. Incorporation of nanosilica into the canola-based polyurethane enhanced both tensile and lap shear strength of synthesized adhesives. Also the effect of nanoparticles on glass transition temperature and thermal stability was investigated by differential scanning calorimetry and thermogravimetric analysis, respectively. The increase of nanosilica content in the polyurethane adhesives, thermal property of the nanocomposites improved.     

Effect of γ-Irradiation on the Dielectric Properties of Poly(methyl methacrylate) Doped with Some Luminescent Materials

A systematic dielectric study over the frequency range from 0.1 to 10 MHz has been carried out on pure and doped poly(methyl methacrylate) (PMMA) with tetracyanoquinodimethane (TCNQ) as an acceptor and rhodamine-6G (Rh-6G) and rhodamine-B (Rh-B) as donors before and after being exposed to γ-irradiation. The results indicate that the addition of TCNQ to PMMA increases its ability to withstand γ-irradiation and improves its insulation properties.     

Effect of γ-Irradiation on the Electrical Properties of Poly (Methyl Methacrylate) Doped with Some Transition Metal Complexes

Abstract

The electrical resistivity (p) of pure and doped poly(methyl methacrylate), PMMA, with dithizone (HDZ) and its metal complexes, Zn(HDZ)₂, Cd(HDZ)₂ and Hg(HDZ)₂ has been investigated before and after γ-irradiation. The results show a phase transition at nearly 323°K. The activation energy of the conduction process has been calculated below and above the transition temperature. Further information concerning the electrical behaviour is obtained by considering the type and mechanism of the conduction process. This has been achieved by studying the effect of temperature and γ-irradiation on the mobility and the number of charge carriers which take part in the conduction process.     

Rheological behaviors and foaming behaviors of crosslinked ethylene–vinyl acetate with polyfunctional monomers

To produce ethylene–vinyl acetate (EVA) foams with a higher foaming ratio and stable cell size, the efficiency of the crosslinking reaction is required to conduct simultaneously with the blowing reaction. Hence, the multifunctional monomer trimethylolpropane trimethacrylate (TMP) as a crosslinking promoter and a crosslinking agent dicumyl peroxide are used together as a crosslinking system to EVA foaming, when chemical blowing agent azodicarbonamide (ADC) is used. The TMP concentration of approximately 1.0 phr (per hundred resin) is most effective for balancing the expansion ratio and fine cell size. In the SEM diagram and expansion ratio results, it can be found that when the concentration of TMP ranges from 0 to 1.0 phr, the cell mean size is reduced from 360.3 to 140.5 μm and the expansion ratio is reduced from 13.6 to 9.1 at 170°C. The results of time-sweep experiment of thermogravimetric analysis (TGA) show that the foaming time of ADC in the melt increases with the addition of TMP. Capillary rheometer and rotational rheometer tests show that the viscosity and the crosslinking efficiency of the melt are improved with the TMP addition. The curing time has been reduced from 2.93 to 2.22 min for 170°C.     

Synthesis and Characterization of Some Poly(1,2-Phenylenedithiocarbamate)–Metal Complexes

Poly(1,2-phenylenedithiocarbamate) (PPDTC) was prepared by the reaction of 2-aminothiophenol with carbon disulfide followed by condensation through the removal of H₂S gas. PPDTC was used as a ligand to prepare four poly(1,2-phenylenedithiocarbamate)–metal complexes of iron(II), cobalt(II), copper(II), and lead(II), by refluxing with the metal salts. The polymer and its metal complexes were investigated by elemental analyses, UV–visible and IR spectroscopy, inherent viscosity, and magnetic susceptibility. The DC electrical conductivity variation with the temperature in the range 298–498 K of PPDTC and its polymeric copper complex was measured. Both polymer and polymer metal complexes showed an increase in electrical conductivity with an increase in temperature: typical semiconductor behavior. The proposed structure of the complexes is (MLX₂·mH₂O) _n .     

Thermal Stabilities and the Thermal Degradation Kinetics of Poly(ε-Caprolactone)

The thermal degradation behavior of poly(ε-caprolactone) (PCL) in nitrogen atmosphere was investigated by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) techniques and Fourier Transform Infrared (FTIR) spectroscopy. TGA/DTG/DSC curves display only one main degradation step. TGA/FTIR results indicate PCL decomposes into CO₂ and hexanoic acid before 500°C. The activation energies were estimated by iterative isoconversional procedure. Friedman plot indicates a change in degradation mechanism. The differential method and integral method were used to confirm the exact kinetic mechanism. The best models are Dn (n = 1, 2, 3, and 4) when 0.08≤a≤0.2 and R2 when 0.25≤a≤0.8.     

Lipase Catalyzed Synthesis and Thermal Properties of Poly(dimethylsiloxane)–Poly(ethylene glycol) Amphiphilic Block Copolymers

Resin immobilized lipase B from Candida antarctica (CALB) was used to catalyze the condensation polymerization of two difuctional siloxane and poly(ethylene glycol) systems. In the first system, 1,3-bis(3-carboxypropyl)tetramethyldisiloxane was reacted with poly(ethylene glycol) (PEG having a number-average molecular weight, M_n = 400, 1000 and 3400 g mol⁻¹, respectively). In the second system, α,ω-(dihydroxy alkyl) terminated poly(dimethylsiloxane) (HAT-PDMS, M_n = 2500 g mol⁻¹) was reacted with α,ω-(diacid) terminated poly(ethylene glycol) (PEG, M_n = 600 g mol⁻¹). All the reactions were carried out in the bulk (without use of solvent) at 80 °C and under reduced pressure (500 mmHg vacuum gauge). The progress of the polyesterification reactions was monitored by analyzing the samples collected at various time intervals using FTIR and GPC. The thermal properties of the copolymers were characterized by DSC and TGA. In particular, the effect of the chain length of the PEG block on the molar mass build up and on the thermal stability of the copolymers was also studied. The thermal stability of the enzymatically synthesized copolymers was found to increase with increased dimethylsiloxane content in the copolymers.     

Surface Energy and Thermal Stability Studies of Poly(dimethyl siloxane)–Poly(alkyl(meth)acrylate) Copolymers

The correlation between the surface energy and thermal stability of polymers plays an important role in engineering of plastic materials. In this work, microstructural characteristics of copolymers of poly(dimethyl siloxane) with benzyl methacrylate, ethyl methacrylate, and methyl acrylate are correlated with their surface energy and thermal stability. The poly(dimethyl siloxane) segments in the copolymer chains affected the hydrophobic behavior. The surface energy of the synthesized copolymers decreased by increasing segments of alkyl methacrylates. The thermal stability of copolymers suggesting that heat resistance of poly(dimethyl siloxane) copolymers used in this correlation can be improved by adjusting the units of alkyl methacrylates in copolymers.     

Composites of Poly(Keto-Sulfide)–Epoxy Resin Systems and Their Thermal and Mechanical Properties

A novel matrix resin system, poly(keto-sulfide)–epoxy resin, has been developed. The poly(keto-sulfide)s (PKS), based on various ketones, formaldehyde, and sodium hydrogen sulfide (NaSH), were prepared by the reported process. These (PKS) having terminal thiol (–SH) groups were used for curing commercial epoxy resin (i.e., diglycidyl ether of bisphenol A – DGEBA), to fabricate crosslinked epoxy-poly(keto-sulfide) resin glass fiber-reinforced composites (GRC). Various epoxy/hardener (PKS) mixing ratios were used, and the curing of epoxy-PKS has been monitored using differential scanning calorimetry (DSC) in dynamic mode. Based on DSC parameters the GRC of epoxy-PKS were prepared and characterized by thermal and mechanical methods. The variation in resin/hardener ratio led to variations in thermal and mechanical properties.     

Effect of γ-Radiation on the Electronic Spectra of Poly(Methyl Methacrylate) Doped with Some Divalent Nd10 Cation Dithizones

The electronic absorption spectra of dithizone (H₂DZ) and its metal complexes of Hg. Cd, and Zn doped in poly(methyl methacrylate), PMMA has been investigated before and after γ-irradiation. It is found that the complex formation resulted in significant changes in both the position and the intensity of the electronic bands of H₂DZ. γ-Radiation causes remarkable decrease in the intensity of the most absorption bands of the metal complexes. The rate of decrease depends on the nature of the metal ions.     

Structure and Performance of Poly(vinyl alcohol)/Poly(γ-benzyl L-glutamate) Blend Membranes

Poly(vinyl alcohol) (PVA)/poly(γ-benzyl L-glutamate) (PBLG) blend membranes with different PBLG wt contents were prepared by pervaporation. Structure and surface morphologies of PVA/PBLG blend membranes were investigated by Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). Thermal, mechanical, and chemical properties of PVA/PBLG blend membrane were studied by differential scanning calorimeter (DSC), tensile strength tests, and other physical methods. It was revealed that the introduction of PBLG homopolymer into PVA could exert an outstanding effect on the properties of PVA membrane.     

Synergistic effect of organically modified layered double hydroxide on thermal and flame-retardant properties of poly(butyl acrylate–vinyl acetate)

Organically modified layered double hydroxide (O-LDH) was successfully synthesized by coprecipitation and characterized through Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). O-LDH/poly(butyl acrylate–vinyl acetate) (P(BA-VAc) emulsion was prepared via in situ polymerization, then ammonium polyphosphate (APP) was introduced to obtain the O-LDH/APP/P(BA-VAc) flame-retardant latex. The flame retardancy and thermal behavior of the latexes after evaporation of water were investigated by the limiting oxygen index (LOI) test, vertical burning test (UL-94), and thermal gravimetric analysis (TGA). Compared with the APP/P(BA-VAc) composite, the LOI value of O-LDH/APP/P(BA-VAc) containing 0.5 wt.% O-LDH at the same total additive loading increased to over 30.0%, and its UL-94 increased from no rating to V-0. TG data show that the amount of residues increases obviously when O-LDH is added. The LOI values increased with increasing amounts of char residues. The morphology and microstructure of residues generated during the LOI test were investigated by scanning electron microscopy (SEM). FTIR and X-ray photoelectron spectroscopy (XPS) were used to determine the composition of the residues formed after combustion at 450 °C for 5 min to support a fundamental analysis of the mechanism of char formation.     

Effect of boric acid treatment on the crystallinity and drawability of poly(vinyl alcohol)–iodine complex films

A film iodinated at solution state before casting (BIBC film) and a film iodinated after casting (BIAC film) were prepared by casting an aqueous solution of poly(vinyl alcohol) (PVA) including I₂/KI and boric acid, and by successively soaking the PVA film in aqueous solutions of boric acid and I₂/KI, respectively. The boric acid-induced and I₂/KI-induced weight gains relative to the PVA were 3, 5, 7, and 10%, and 3, 5, 10, and 20%, respectively. The effects of boric acid and iodine on the crystallinity and drawability of the films were investigated. Although the crystalline structure of the BIAC films was not affected by boric acid, the boric acids in the PVA solution containing I₂/KI may have formed intra-molecular cross-links on the PVA chain to accelerate the formation of the PVA–iodine complex evenly, and subsequently interrupt the PVA crystallization through the BIBC film formation to render the resultant film slightly crystalline or practically amorphous. This occurred even at a much lower I₂/KI-induced weight gain (20%) than the minimum weight gain (125%) at which the iodinated at solution state before casting film without boric acid indicated a practically amorphous state. The maximum draw ratio of the films generally decreased with increasing boric acid content, which was mainly attributed to the increase of the extended segments of the PVA chains in the amorphous region due to the cross-links formed with the boric acids. The maximum draw ratios of the BIBC films tended to decrease more severely than those of the BIAC films.     

Modeling of interdiffusion in poly(vinyl acetate)–poly(methyl methacrylate)–toluene multicomponent systems

Work on interdiffusion has been mainly carried out in binary systems in the past, and this work has focused on polymer–solvent (S) systems and polymer blends. To understand and predict the interdiffusion of two solids in the presence of one S, we present a new mathematical model based on the Onsager approach. Within our model, interdiffusion kinetics are described with a modification of the reptation model for long polymer chains, and the chemical potential gradient is used as the driving force behind mass transfer. The chemical potential is calculated with a Flory–Huggins approach. The model was validated with 29 Raman spectroscopy experiments in poly(vinyl acetate)–poly(methyl methacrylate)–toluene systems at 20 °C. Monomer mobilities (L _i,0s) were determined for both polymers to show the independence of L _i,0 from the chain length. The L _i,0s were found to be strongly dependent on the S content. With the knowledge of phase equilibria and L _i,0s, interdiffusion in the ternary polymer–polymer–S system could be predicted by the introduced model. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47092.     

Thermal decomposition of cerium(III) acetate studied with sample-controlled thermogravimetric–mass spectrometry (SCTG—MS)

Thermal decomposition of cerium(III) acetate hydrate, Ce(CH₃CO₂)₃·1.5H₂O, to cerium(IV) oxide, CeO₂, in helium has been successfully investigated by sample-controlled thermogravimetry combined with evolved gas analysis by mass-spectrometry (SCTG–MS). Cerium(III) anhydrous acetate decomposed to cerium (IV) oxide through four decomposition steps in the temperature range of 250–800 °C. SCTG–MS was very useful to distinguish the successive decomposition accompanying the formation of the intermediate products to identify simultaneous gas evolution during the mass losses. The decomposition intermediates quenched from SCTG were characterized by X-ray diffraction (XRD) and X-ray absorption near-edge structure (XANES). The XANES revealed clearly the coexistence of Ce(III) and Ce(IV) and the valence change from cerium(III) to cerium(IV). The three decomposition intermediate products were presumed to be Ce₂O(CH₃CO₂)₄, Ce₂O₂(CH₃CO₂)₂ and Ce₂O₂CO₃. A detailed thermal decomposition mechanism of Ce(CH₃CO₂)₃·1.5H₂O is discussed.     

Synthesis,Characterization of Fulvic Acid–Poly(Methylmethacrylate) Graft Copolymers Based on Surface-Initiated Atom Transfer Radical Polymerization and its Effect on Performance of Poly(Lactic Acid)

Fulvic acid–poly(methylmethacrylate) graft copolymers were synthesized by surface-initiated atom transfer radical polymerization with fulvic acid. The result demonstrated that the hydrophobicity of fulvic acid–poly(methylmethacrylate) was improved after modification by surface-initiated atom transfer radical polymerization. Furthermore, poly(lactic acid)/fulvic acid–poly(methylmethacrylate) composites were prepared to improve the performances of poly(lactic acid) by blend melting. Compared to poly(lactic acid) with X_c of 5.38%, the X_c of poly(lactic acid)/fulvic acid–poly(methylmethacrylate) composites was 19.94%. Moreover, the impact strength of poly(lactic acid)/fulvic acid–poly(methylmethacrylate) composites was increased by 5.19% compared to poly(lactic acid). In all, this study provided an effective and feasible method for optimizing interface performance and enhancing the thermal stability of poly(lactic acid).     

Preparation of Poly(Vinyl Alcohol) Nanocomposite Films Reinforced with Poly(Amide–Imide)/CuO Having N-trimellitylimido-L-valine Linkages for the Improvement of Mechanical and Thermal Properties

In this investigation, nanocomposite films were fabricated by dispersion of poly(amide–imide)/CuO nanocomposites as nanofiller in the poly(vinyl alcohol) matrix via an ultrasonic process. The nanofiller was prepared and mixed with PVA matrix. After dispersion of nanofiller into the poly(vinyl alcohol), the mechanical properties of the nanocomposites were improved. For example, the addition of 6 wt% nanofiller into the poly(vinyl alcohol) matrix enhanced the tensile modulus by 39%. The residual weight at 800°C was 7% for pure poly(vinyl alcohol) while the nanocomposites illustrated 12–19% residue at this temperature.     

Effect of Polysaccharides on the Properties of the Mucoadhesive Poly(Vinyl Alcohol) Multicore–Shell Microparticles

This study discusses about the effect of polysaccharides (agar, gum tragacanth, and guar gum) on the properties of the core (organogel)–shell [poly(vinyl alcohol)] microparticles. The size, swelling, and mucoadhesive properties of the poly(vinyl alcohol) microparticles were altered in the presence of the polysaccharides. Thermal analysis confirmed the presence of organogels within the microparticles. Fourier transform infrared spectroscopy confirmed the presence of the polysaccharides within the microparticles. The microparticles were biocompatible in nature. Drug release indicated that an alteration in the shell composition can be used for altering drug release. Ciprofloxacin-loaded microparticles showed sufficient antimicrobial efficiency.     

A Hybrid Membrane of Poly(vinyl alcohol) and Phosphotungstic Acid for Fuel Cells

Proton conducting membranes composed of phosphotungstic acid (PWA) and poly(vinyl alcohol) (PVA) were prepared. Conductivity and Fourier transform infrared spectrometer(FTIR) measurements show that most of the acid embedded are stable in the PVA matrix when the membrane is immerged in water or methanol solution at room temperature. Conductivity of the composite membranes scatters around 10-3S·cm-1 at room temperature. The methanol crossover through the membranes is about an order of magnitude lower than that through Nafion 117 membrane.