Effect of thermal oxidative ageing on the morphology of natural rubber networks as viewed by ESR

The change of network morphology of unfilled sulfur crosslinked natural rubber exposed to thermal oxidative ageing has been studied. Three model networks with different sulfur contents (efficient network, semi‐efficient and conventional vulcanizate) have been analysed by applying spin probe ESR, equilibrium swelling measurements and mechanical measurements. By combining the density distribution deduced from the complex ESR spectra and the equilibrium swelling density, it is shown that the major network changes occur in the networks with predominantly polysulfidic bonds (conventional network) after 96 h of ageing at 373 K. The effect of ageing on the network with predominantly monosulfidic bonds is much less pronounced. Both effects (main chain scission and additional local crosslinking) have been analysed in the course of prolonged ageing up to 240 h. A correlation between network structure and its mechanical performance is established. © 2000 Society of Chemical Industry     

Influence of γ-irradiation on proton spin–lattice relaxation of SBR used as antirads and its ESR investigation

Proton spin–lattice relaxation time t₁ was measured on SBR samples with carbon black or kaolin filler using modified linseed oil. The NMR pulse technique at 90MHz was used in the temperature range from 180 to 400 K. The temperature dependence of t₁ indicates that samples filled with carbon black have similar molecular dynamics to the standard unfilled SBR samples. The activation energy for the motion of the main chain for these samples amounts to 16.4kJ/mol. Samples containing linseed oil modified with para-toluidine showed an activation energy of about 14.6kJ/mol and were not affected by γ-irradiation. Values of the minimum relaxation time t^min₁ were increased by γ-irradiation in comparison with a standard SBR sample. ESR measurements carried out at room temperature by means of an X-band spectrometer indicated that unidentified radicals within the rubber were formed during its mastication with vulcanizing additives. The ESR spectra did not change during the vulcanization process. Samples filled with carbon black showed a broadening of the ESR line; this is consistent with the increase in the electrical conductivity.     

Synthesis and characterization of the two novel liquid crystalline epoxy resins based on bisphenol‐s mesogen

Two novel liquid crystalline epoxy resins (LCER) based on bisphenol‐S mesogen, 4,4′‐Bis‐(2,3‐epoxypropyloxy)‐sulfonyl bis(1,4‐phenylene) (p‐BEPSBP) and sulfonyl bis(4,1‐phenylene) bis[4‐(2,3‐epoxypropyloxy)benzoate] (p‐SBPEPB), were synthesized. Their liquid crystalline behavior and structure were characterized by Fourier transmittance infrared ray (FTIR), differential scanning calorimetry (DSC), ¹HNMR, polarized optical microscopy (POM) and X‐ray diffraction (XRD). The results show that p‐BEPSBP is a kind of thermotropic liquid crystal and has a smectic mesophase with a melting point (T_m) at 165°C; the p‐SBPEPB is a kind of nematic mesophase with the temperature range of 155–302°C from the T_m to the clearing point T_i. The curing behaviors and texture of the liquid crystalline epoxy resins with 4,4′‐diaminodiphenyl ether (DDE) were also studied by DSC and some kinetic parameters were evaluated according to the Ozawa's method. The dynamic mechanical properties of curing products were also investigated by torsional braid analysis (TBA), and the results suggest that the dynamic mechanical loss peak temperature (T_p) of p‐BEPSBP/DDE and p‐SBPEPB/DDE is 120 and 130°C, respectively. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Spin probe study of semi‐interpenetrating polymer networks based on polyurethane and polymethacrylate functional prepolymers

The motional transition and heterogeneity of semi‐interpenetrating networks (SIPNs) based on polyurethane (PU) with carboxylic groups and methacrylic copolymer (PM) with tertiary amine groups were studied by the electron spin resonance (ESR) spin probe method. The concentration of functional groups in both prepolymers varied from 0 to 0.45 mmol g^?1. Spin‐probed SIPNs show that the temperature‐dependent spectra are sensitive to polymer interactions imposed by functional groups. These interactions determine the free volume distribution in the matrix and temperature at which motional transition takes place. The fraction of free volume increases with functional group concentration and reaches its maximum at 0.25 mmol g^?1. Further increases in the functional group concentration reduce the free volume. The results of the networks with strong interactions are discussed in terms of the interference of the plasticizing effect of the PU component and the formation of possible cluster cross‐links, which restricts segmental motions. Copyright © 2003 Society of Chemical Industry     

High‐solids mar resistant clearcoats prepared from an isophthalate‐based oligoester and a melamine resin. Study and characterization of mar resistance with scanning probe microscopy method

A new series of high‐solids [low‐VOC (volatile organic compound)content] mar resistant clearcoats (CL‐series) were prepared upon crosslinking of a new‐synthesized hydroxyl‐terminated isophthalate‐based liquid oligoester (L‐311) with an hexakis(methoxymethylol)melamine (HMMM) resin, via an acid‐catalyzed etherification reaction. The chemical, physical, and mechanical properties of the CL‐clearcoats were compared to those of a reference clearcoat (CRO). An attempt was made to investigate the effect that the amounts of catalyst and melamine resin had on the clearcoats' physical, chemical, and mechanical properties, and moreover, to correlate these properties to the films chemical structures. The new‐formulated high‐solids clearcoats (CL‐series) presented enhanced processability and higher NVW values (lower VOC content) than the reference clearcoat CRO, and their properties (pencil hardness, knoop hardness, adhesion, impact resistance, solvent and gasoline resistance, mar resistance, and flexibility) were better or comparable to those of the CRO. More specifically, the mar resistance of the CL‐clearcoats series was investigated by applying both the crockmeter test and a novel method that employed a modified scanning probe microscope. In addition, we identified and characterized the different responses of the CRO and certain CL‐clearcoats to marring stress. The experimental data regarding the mar resistance of the new‐formulated clearcoats fully justified our polymer design strategy, verifying our expectations for the possibility of preparing glossy, high‐solids mar‐resistant clearcoats that could present enhanced processability and solvent resistance, relatively high pencil hardness, and at the same time very good elastic recovery to marring stress. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1317–1333, 2002     

Itaconic acid used as a versatile building block for the synthesis of renewable resource‐based resins and polyesters for future prospective: a review

Itaconic acid, a carbohydrate‐derived aliphatic dicarboxylic acid, is a potential chemical for the synthesis of renewable resource‐based resins and polyesters. Owing to environmental reasons, there is a gradual demand for renewable resources in the chemical industry. Conversely, as a rather underappreciated side effect of this growth, novel chemical building blocks are obtained, which are not commercially derived from petrochemical sources. In this respect, itaconic acid has attracted much attention and its trifunctional structure leads to the synthesis of novel polymeric materials. This review discusses the most relevant information for bio‐based resins and polyesters resulting from itaconic acid and distinctive properties for various commercial applications. © 2017 Society of Chemical Industry     

Influence of electron donors on the initial stage of cyclopolymerization of 1,5‐hexadiene with MgCl2‐supported Ziegler catalysts analyzed by temperature rising elution fractionation

Additive effects of donors on the initial polymerization of 1,5‐hexadiene with the MgCl₂‐supported Ziegler catalysts were investigated by using the stopped‐flow method, temperature rising elution fractionation (TREF) analysis, and kinetic study. The cyclopolymerization of 1,5‐hexadiene proceeded within an extremely short period (≤ 0.2 s) and yielded a unique poly(methylene‐1,3‐cyclopentane). cis ring content and cis–cis unit in meso dyad of the resulting polymer were increased by the addition of electron donors. The influence of internal and external donors was examined by the estimation of kinetic parameters and TREF analysis. Because the addition of the internal donor caused an obvious change in one of the kinetic parameters and the microstructure, an isospecific active site was considered to be formed by the addition of the internal donor. In the case of the external donor, the additive effects on the stereospecificity were weaker than those of the internal donor. It was expected from TREF measurements that the external donor modified an aspecific active site into a lower isospecific active site. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2976–2983, 2002; DOI 10.1002/app.2326     

Sorption of binary liquid mixtures in methacrylate‐based biomaterials; Simultaneous determination of the diffusion coefficients and the uptake fraction at equilibrium of the components of ethanol‐water mixtures by a new iterative method

The present investigation is concerned with the development of a new iterative method permitting, for a Fickian sorption of a binary liquid mixture in thin polymer sheets, the simultaneous determination of the self‐diffusion coefficients of the components of the mixture, and their uptake fractions at equilibrium. The approach is based on a new equation describing a parallel Fickian sorption of the components of the mixture into thin polymer sheets. The procedure was tested with ideal and Monte Carlo simulated data. The method, applied to ideal simulated data that corresponded to various values of D₁, D₂ and f, perfectly extracted the desired parameters. The application of the method to Monte Carlo simulated data revealed that this method is fairly applicable even when the simulated data are considerably obscured by “noise”. Finally, the proposed method was successfully applied to the experimental data concerning the sorption kinetics of ethanol–water mixture (75 vol % in EtOH) at 37°C in thin polymeric sheets of triethyleneglycol dimethacrylate (TEGDMA). © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008