scispace - formally typeset
Search or ask a question

Showing papers in "Polymer Engineering and Science in 1989"


Journal ArticleDOI
TL;DR: In this paper, the fracture properties of the weld, namely, fracture stress, σ, fracture energy, GIc, fatigue crack propagation rate da/dN, and microscopic aspects of the deformation process are determined using compact tension, wedge cleavage, and double cantilever beam healing experiments.
Abstract: Studies of strength development at polymer-polymer interfaces are examined and applications to welding of similar and dissimilar polymers are considered. The fracture properties of the weld, namely, fracture stress, σ, fracture energy, GIc, fatigue crack propagation rate da/dN, and microscopic aspects of the deformation process are determined using compact tension, wedge cleavage, and double cantilever beam healing experiments. The mechanical properties are related to the structure of the interface via microscopic deformation mechanisms involving disentanglement and bond rupture. The time dependent structure of the welding interface is determined in terms of the molecular dynamics of the polymer chains, the chemical compatibility, and the fractal nature of diffuse interfaces. Several experimental methods are used to probe the weld structure and compare with theoretical scaling laws, Results are given for symmetric amorphous welds, incompatible and compatible asymmetric amorphous welds, incompatible semicrystalline and polymer-metal welds. The relevance of interface healing studies to thermal, friction, solvent and ultrasonic welds is discussed.

305 citations


Journal ArticleDOI
TL;DR: In this paper, the main advantages and disadvantages of different welding techniques, together with their main disadvantages, are briefly described and a selective bibliography, in which the 259 references have been arranged chronologically for each technology type, provides a guide to the literature.
Abstract: Joining of plastics and plastic composites is becoming important because of the emerging structural applications of these materials. While providing an overview of all joining methods, this paper emphasizes the welding of thermoplastic materials. Different welding techniques, together with their main advantages and disadvantages, are briefly described. A selective bibliography, in which the 259 references have been arranged chronologically for each technology type, provides a guide to the literature.

215 citations


Journal ArticleDOI
TL;DR: In this paper, the effect of deformation history on the morphology and properties of liquid crystalline polymers (LCP) blended with polycarbonate resin was assessed and the addition of an immiscible LCP phase was found to improve the melt processability of the host thermoplastic polymer.
Abstract: The effect of deformation history on the morphology and properties of liquid crystalline polymers (LCP) blended with polycarbonate resin was assessed. The addition of an immiscible LCP phase was found to improve the melt processability of the host thermoplastic polymer. In addition, by employing a suitable deformation history, the LCP phase may be elongated and oriented such that a microfibrillar morphology can be retained in the solid state.

157 citations


Journal ArticleDOI
TL;DR: In this paper, the authors used a five part model that includes mechanics and vibration of the parts, viscoelastic heating, heat transfer, flow and wetting, and intermolecular diffusion.
Abstract: The ultrasonic welding process is modeled using a five part model that includes mechanics and vibration of the parts, viscoelastic heating, heat transfer, flow and wetting, and intermolecular diffusion. The model predicts that melting and flow occur in steps, which has been confirmed by experiments. The model also indicates the possibility of monitoring joint quality by measuring the dynamic mechanical impedance of the parts during welding, which has also been verified experimentally by indirectly monitoring the magnitude of the impedance. via measurements of both the power and the acceleration of the base. When the melt fronts of the energy directors meet, at the end of welding, the dynamic impedance of the composites' interface is shown to rise rapidly. This raises the possibility of developing closed loop control procedures for the ultrasonic welding of thermoplastic composites. Ultrasonic welding of polyetheretherketone (PEEK) graphite APC-2 composites produced joints with excellent strengths.

151 citations


Journal ArticleDOI
TL;DR: In this paper, a mixture of polycarbonate (PC) and poly(ethylene terephthalate-co-p-oxybenzoate) (PET/PHB60) was prepared by melt-blending.
Abstract: Blends of polycarbonate (PC) and poly(ethylene terephthalate-co-p-oxybenzoate) (PET/PHB60) were prepared by melt-blending. Physical and/or chemical interactions between the two phases of the system were studied by thermal analysis and infrared spectroscopy. Rheological measurements in shear flow were carried out both in the low and high shear rate regions in the temperature range of the existence of the mesophase. At low liquid crystalline polymer (LCP) content, the blends showed flow curves similar to those of the unfilled PC, while at higher LCP percentages the rheological behavior of the pure LCP was resembled. Moreover, in the whole shear range, the viscosity values of such blends were in between those of the pure polymers. The influence of the addition of 10% LCP on the mechanical properties of the PC was investigated. Fiber-spinning was performed under different experimental conditions, and it was found that opportune drawing conditions are necessary to improve the modulus of the matrix. Morphological analyses of the pure LCP and of the blends were related to the rheological and mechanical behavior of these systems. While the LCP exhibited an elevated dimensional stability, the inclusion of the LCP in PC matrix did not improve the dimensional stability of the blends.

126 citations


Journal ArticleDOI
TL;DR: A review of the literature dealing with adhesive bonding of polymer matrix composite structures can be found in this paper, where the authors present a review of adhesive bonding for thermoplastic polymer matrix composites.
Abstract: In structures composed of polymer matrix composite materials, components must be joined such that the overall structure retains its structural integrity while it is performing its, intended function which can include both mechanical loads (static and dynamic) and environmental loads (temperature and humidity). The use of composite materials in complex structures almost always reduces the number of components in the structures compared to the use of metallic alloys for the same structure. Thus, using composite materials not only results in great savings in weight, but also through a reduced number of joining operations, results in significant savings in assembly, inspection, parts storage, and movement, resulting in increased reliability and lower cost. Yet joining is still required. Joining metallic structures is a mature technology involving riveting, bolting, welding, glueing, brazing, soldering, and other methods. However, for most polymer matrix composites only adhesive bonding and mechanical fastening can be utilized. Attention has been given recently, however, to localized welding of thermoplastic polymer matrix composites, and this will be discussed briefly later. Inherently, adhesive bonding is preferable to mechanical fastening because of the continuous connection, whereas in drilling holes for bolts or rivets, fibers or other reinforcements are cut, and large stress concentrations occar at each discrete fastener hole. The following is a review of much of the literature dealing with adhesive bonding of polymer matrix composite structures. It is Intended not only to be a review, but also a background for detailed study of the referenced and other documents, and a catalyst for future research.

120 citations


Journal ArticleDOI
TL;DR: In this paper, the thermomechanical stability of a number of organosilane surface treatments for glass fibers was evaluated for use in a fiber reinforced epoxy resins.
Abstract: The thermomechanical stability of a number of organosilane surface treatments for glass fibers was evaluated for use in a fiber reinforced epoxy resin. All of the silane coatings were found to improve the tensile strength of E-glass filaments, particularly at large gauge lengths. A phenylamino silane and an amino silane were particularly effective in this regard. The fiber/matrix interface was evaluated as a function of temperature and after exposure to boiling water using a single-fiber composite test. All silane coatings transmitted a higher interfacial shear stress than obtained in composites with no coatings, and in all cases the shear stress transmission was considerably higher than would be expected from the yield properties of the resin. Measurements of the glass transition temperature of the epoxy resin, as well as Fourier-Transform Infra-Red analysis, indicated modification of resin properties in a zone around the glass fibers. Each of the silane coatings provided more stable thermomechanical properties than those obtained with uncoated glass, at least until the silanes were irreversibly degraded by boiling water. A phenylamino silane provided the most thermally stable properties. Finally, unidirectional E-glass fiber reinforced laminae were fabricated and the measured values of longitudinal strength were compared favorably to theoretical predictions.

109 citations


Journal ArticleDOI
TL;DR: In this paper, the mechanical and rheological properties of blends of a thermotropic liquid crystalline polyester with a polycarbonate have been investigated by performing solid state relaxation measurements and the relaxation modulus was also found to increase by the addition of LCP.
Abstract: Mechanical and rheological properties of blends of a thermotropic liquid crystalline polyester with a polycarbonate have been investigated. The blends are fibrillar in character and exhibit great hardness and toughness due to high degree of molecular orientation which develops during the melt blending and processing steps. Increases of the Young modulus by 100 percent are observed for blends containing only 10 percent of liquid crystalline polymer, LCP. Time-dependent behavior of the blends was investigated by performing solid state relaxation measurements and the relaxation modulus was also found to increase by the addition of LCP. The effect is relatively small in the glassy zone of viscoelastic response, but increases through the transition and viscous flow regions. The melt viscosity of the polycarbonate is slightly shear thinning whereas that of the unblended LCP increases rapidly with decreasing shear rate at low shear rate. This suggests the presence of yield stresses as confirmed by measurements on the Rheometics RSR in the stress sweep mode. The melt viscosity of the blends was found to be similar to that of the unblended polycarbonate, but more shear-thinning and less viscous. Preliminary results of scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) are also presented.

102 citations


Journal ArticleDOI
TL;DR: In this article, the effect of molecular weight distribution on the rheological and mechanical properties of a series of polypropylenes was evaluated, which were produced by controlled chemical degradation in a single-screw extruder.
Abstract: The effect of molecular weight distribution on the rheological and mechanical properties of a series of polypropylenes is evaluated. The polypropylenes tested were produced by controlled chemical degradation in a single-screw plasticating extruder. Measured properties include shear, extensional and intrinsic viscosity, melt flow index, extrudate swell, melting and crystallization temperatures, impact strength, flexural modulus, and tensile stress.

96 citations


Journal ArticleDOI
TL;DR: In this article, the authors investigated the near-field ultrasonic welding of amorphous (acrylonitrile-butadiene-styrene and polystyrene) and semicrystalline (polyethylene and polypropylene) polymers.
Abstract: Ultrasonic welding is one of the most popular techniques for joining thermoplastics because it is fast, economical, and easily automated. In near-field ultrasonic welding, the distance between the horn and the joint interface is 6 mm or less. This study investigated the near-field ultrasonic welding of amorphous (acrylonitrile-butadiene-styrene and polystyrene) and semicrystalline (polyethylene and polypropylene) polymers. High frequency ultrasonic wave propagation and attenuation measurements were made in order to estimate the dynamic mechanical moduli of the polymers. The estimated moduli were entered into a lumped parameter model in order to predict heating rates and energy dissipation. Experimental results showed that variations in the welding pressure had little effect on energy dissipation or joint strength; Increasing the amplitude of vibration increased the energy dissipation and the weld strength. For the semicrystalline polymers, increasing the weld time improved strength up to weld times greater than 1.5 s, where strength leveled off. For the amorphous polymers, the weld strength increased with Increasing weld time up to times of 0.8 s; for longer weld times, the power required was too high, causing overloading of the welder. Monitoring of the energy dissipation and static displacement or collapse provided valuable information on weld quality.

95 citations


Journal ArticleDOI
TL;DR: A sliding plate rheometer has been developed that is suitable for use with molten plastics, concentrated polymer solutions, raw elastomers, and other viscoelastic or thixotropic materials.
Abstract: A novel sliding plate rheometer has been developed that is suitable for use with molten plastics, concentrated polymer solutions, raw elastomers, and other viscoelastic or thixotropic materials. It can generate steady shear rates from 0.05 to 500 s−1 and can also be used to measure linear viscoelastic properties. In addition, it can be used to measure a broad spectrum of nonlinear viscoelastic properties such as the nonlinear relaxation modulus and the shear stress growth coefficient. In order to measure these nonlinear properties it is necessary to generate large, uniform, transient deformations Involving high strain rates. Rotational and capillary melt rheometers are not capable of generating this type of deformation, and until now it was not convenient to use sliding plate rheometers for this type of application. However, the recent development of a reliable and robust shear stress transducer makes it very convenient to use the sliding plate geometry to carry out all of these tests. The new rheometer is described, and examples of the types of data it can generate are shown.

Journal ArticleDOI
TL;DR: A methodological survey of preparation of microspheres and microcapsules by suspension cross-linking is presented in this paper, where the formation of small droplets of a polymer solution (or melt) in an immiscible liquid followed by hardening of these droplets by covalent crosslinking, are discussed.
Abstract: A methodological survey of preparation of microspheres and microcapsules by suspension cross-linking is presented. Thus, basic features of suspension cross-linking, i.e., the formation of small droplets of a polymer solution (or melt) in an immiscible liquid followed by hardening of these droplets by covalent cross-linking, are discussed. Typical microspherical and microcapsular products manufactured by suspension cross-linking of naturally occurring and preformed synthetic polymers, including agarose and cellulose beads, albumin microspheres and microcapsules, polystyrene beads and epoxy resin microcapsules, are described. Manufacturing parameters controlling microsphere/microcapsule characteristics are also briefly outlined.

Journal ArticleDOI
TL;DR: In this paper, the rheological and thermokinetic aspects of the cure of epoxy based composite laminates are analyzed by means of a computer program developed using the heat transfer and heat generating characteristics of a polymerizable system.
Abstract: The rheological and thermokinetic aspects of the cure of epoxy based composite laminates are analyzed by means of a computer program developed using the heat transfer and heat generating characteristics of a polymerizable system. In particular, the temperature and degree of cure influence on the resin viscosity have been first considered, then the temperature profiles, calculated according to an appropriate kinetic and heat transfer modeling, have been used to predict the corresponding viscosity profiles. Molecular and thermocalorimetric parameters are used for the prediction of the theoretical chemorheological behavior. Commercial epoxy systems commonly used in the preparation of carbon fiber laminates have been characterized by Differential Scanning Calorimetry (DSC) and dynamic viscosity measurements and the results are compared with the theoretically predicted values.

Journal ArticleDOI
TL;DR: In this paper, a two-phase structure was formed, consisting of spherical rubber particles dispersed in an epoxy matrix, and a broad distribution of rubber particles was observed in all the materials with most of the particles ranging in size from 1 to 4 μm, but some particles exceeding 20 μm.
Abstract: Epoxies toughened with two reactive liquid rubbers, an epoxy-terminated butadiene acrylonitrile rubber (ETBN) and an amino-terminated butadiene acrylonitrile rubber (ATBN), were prepared and studied in terms of their structure property relationships. A two-phase structure was formed, consisting of spherical rubber particles dispersed in an epoxy matrix. A broad distribution of rubber particles was observed in all the materials with most of the particles ranging in size from 1 to 4 μm, but some particles exceeding 20 μm were also found. Impact strength, plane strain fracture toughness (KIC), and fracture energy (GIC) were increased, while Young's modulus and yield strength decreased slightly with increasing rubber content and volume fraction of the dispersed phase. Both GIC and KIC were found to increase with increasing apparent molecular weight between crosslinks and decreasing yield strength. The increased size of the plastic zone at the crack tip associated with decreasing yield strength could be the cause of the increased toughness. An ATBN-toughened system containing the greatest amount of epoxy sub-inclusion in the rubbery phase demonstrated the best fracture toughness in this series. In the present systems, rubber-enhanced shear deformation of the matrix is considered to be the major toughening mechanism. Curing conditions and the miscibility between the liquid rubber and the epoxy resin determine the phase morphology of the resulting two-phase systems. Kerner's equation successfully describes the modulus dependence on volume fraction for the two-phase epoxy materials.

Journal ArticleDOI
TL;DR: In this paper, the authors show that flow-induced phase separation occurs in both shear flow and extensional flow in polystyrene with poly(vinyl methyl ether) blends.
Abstract: Shear and extensional flows can have a significant effect on the miscibility for a blend of polystyrene with poly(vinyl methyl ether). The cloud point temperature in a planar stagnation flow is elevated by as much as 12 K; the magnitude depends on the extension rate, the strain, and the blend composition. Flow-induced miscibility is also observed in the shear flow between parallel plates which has been used to test smaller samples and to prepare solid samples for further characterization. At lower temperatures, as much as 30 K below the coexistence temperature, flow-induced phase separation occurs in both shear flow and extensional flows. The stress, rather than deformation rate, appears to be the most important parameter in flow-induced phase separation.

Journal ArticleDOI
TL;DR: In this paper, a phenomenological model for the reaction rate expression and differential scanning calorimetry (DSC) data from isothermal and non-isothermal experiments is presented. But the authors do not consider the effect of vitrification.
Abstract: Differential Scanning Calorimetry (DSC) is a popular method for the characterization of the cure kinetics of thermosetting materials. The experiments may be carried out under isothermal or temperature program modes. Several authors have pointed out the fact that the kinetic rate expressions for non-isothermal experiments must be different from the isothermal ones; however, this fact has been neglected in practice. In this work, we present a kinetic characterization of a thermosetting system using a phenomenological model for the reaction rate expression and DSC data from isothermal and non-isothermal experiments. In general, thermosetting materials exhibit the vitrification phenomenon which stops the reaction before complete conversion is achieved. Vitrification is taken into account in both Isothermal and temperature programmed experiments.

Journal ArticleDOI
TL;DR: In this paper, nonisothermal differential scanning calorimetry (DSC) measurements were used to estimate the kinetic parameters for the curing reaction of a commercial unsaturated polyester resin.
Abstract: Nonisothermal differential scanning calorimetry (DSC) measurements were used to estimate the kinetic parameters for the curing reaction of a commercial unsaturated polyester resin. The reaction rate expression was derived from a mechanistic kinetic model based on the concept of free radical polymerization, accounting also for the diffusion controlled reaction. The total heat of reaction was evaluated in experiments run at very low scan speeds and using high amount of initiator. The kinetic parameters were found to show no dependency on the heating rate nor on the initiator concentration. Dynamic DSC measurements provide reliable kinetic data over a broad range of temperatures that is mostly significant for process simulations.

Journal ArticleDOI
TL;DR: In this article, fracture toughness characterization of four impact-modified polymers based on the J-integral concept was studied, and it was found that the use of the blunting line fails to specify properly the critical Jintegral value for crack initiation.
Abstract: The fracture toughness characterization of four impact-modified polymers based on the J-integral concept was studied. We have discovered that the use of the “crack blunting line” concept needs revision. Direct measurements of the crack growth can be made (as opposed to indirect readings from the fracture surface) that test the applicability of the crack blunting concept. Our results indicate that for rubber-toughened polymers the use of the blunting line fails to specify properly the critical J-integral value for crack initiation.

Journal ArticleDOI
TL;DR: In this paper, the properties of linear polyesters have been investigated in crystalline, liquid crystalline and amorphous phases and the conditions for transreaction have been determined and the properties measured for the resultant new copolymers.
Abstract: Thermal and mechanical studies on many linear polyesters have revealed their behavior in crystalline, liquid crystalline, and amorphous phases. Their phase behavior in binary compositions has also been studied by a range of additional techniques and in combinations including the polycarbonate of bisphenol-A. Regions of amorphous compatibility and incompatibility have been identified and measures made of transition temperature changes with composition. The conditions for transreaction have also been determined and the properties measured for the resultant new copolymers.

Journal ArticleDOI
TL;DR: In this paper, the authors describe the synthesis, characterization, and lithographic evaluations of novel positive photoresists based on hydroxy polyimides and polyamides containing 6-F linking groups.
Abstract: In this paper we describe the synthesis, characterization, and lithographic evaluations of novel positive photoresists based on hydroxy polyimides and polyamides containing 6-F linking groups. The polymers were synthesized using solution condensation techniques and characterized using solution viscosity, GPC, FTIR, NMR, UV, TGA, and DSC. Tg's of these polymers range from 250 to 300°C. Both polyimides and polyamides are soluble in a variety of solvents commonly utilized for photoresist applications. When formulated with diazonaphthoquinone sensitizers, these polymers provide an improved high-temperature resistant, aqueous base developable positive photoresist system with good photospeed, contrast, and resolution characteristics. High resolution relief images were obtained which are comparable to 1300 Series AZ type photoresists. No thermal deformation, loss in resolution or defects were noticed when relief patterns were annealed to 250°C. Additionally, the hydroxy polyamide based resists, when thermally annealed to 300°C, provide a photoresist system with even higher thermal stability (400 to 450°C) and excellent resistance to solvents. Also, the photoresist formulations have excellent storage stability at room temperature and can be processed like conventional positive photoresists using broad band UV radiation sources.

Journal ArticleDOI
Chul Rim Choe1, Kwang Hee Lee1
TL;DR: In this paper, a new kinetic model for nonisothermal crystallization of poly(etheretherketone) was derived and the possibility of its application was investigated by evaluating the parameters in the model, the crystallization behavior of PEEK was analyzed.
Abstract: Analysis of the crystallization kinetics of poly(etheretherketone) (PEEK) was achieved with dynamic differential scanning calorimetry results. A new kinetic model for the nonisothermal crystallization was derived and the possibility of its application was investigated. By evaluating the parameters in the model, the crystallization behavior of PEEK was analyzed. The experimental and predicted crystallinity change showed good agreement, which indicated that the model equation was appropriate to describe the nonisothermal crystallization kinetics of PEEK. As the melt temperature was increased the number of heterogeneous nuclei decreased, hence the crystallization was delayed.

Journal ArticleDOI
TL;DR: The long term stability of PTMSP has been determined by a combination of thermal gravimetric analysis (TGA) and permeability test procedures under a number of different isothermal aging conditions.
Abstract: Poly[1-(trimethylsilyl)propyne] (PTMSP) is an unusual polyyne material which is optically clear, exhibits high solubility in nonpolar organic solvents, and good oxygen compatibility. By contrast, polyacetylene is black, insoluble, and is unstable in oxygen. The long term stability of PTMSP has been determined by a combination of thermal gravimetric analysis (TGA) and permeability test procedures under a number of different isothermal aging conditions. The use of commercial antioxidants at up to 2 weight percent improves the long term stability of PTMSP. The presence of the antioxidant has no effect on the surface fluorination of PTMSP. Testing of PTMSP films for over eight months shows no change in either permeability or selectivity in contrast to previously reported data.

Journal ArticleDOI
TL;DR: In this article, a mathematical relationship between the experimentally obtained signals and the physical state of the polymer was developed to account for the dielectric response during both isothermal and dynamic cure experiments.
Abstract: Using dielectric techniques to monitor thermoset properties on-line during processing requires a mathematical relationship between the experimentally obtained signals and the physical state of the polymer. Such a relationship accounting for the dielectric response during both isothermal and dynamic cure experiments is developed in this study. Ionic conductivity changes with cure were described using the Keinle-Race expression, while an approach taken by Lane, Bachmann, and Seferis for modeling dipolar relaxation during isothermal cure was extended to nonisothermal cure conditions. Both of these approaches were combined in this study, providing a complete description of the dielectric changes occurring in thermosetting systems resulting from cure. Experimental results for a model epoxy/amine system were predicted with the developed methodology for isothermal cure at 140°C, 150°C, 160°C, and 170°C and cure under dynamic heating conditions at 1°C per minute.

Journal ArticleDOI
TL;DR: In this paper, the effect of physical aging on viscoelastic properties was studied for several cross-linked epoxies in the glassy state, and the dependence of to on the aging time was determined.
Abstract: The effect of physical aging on viscoelastic properties was studied for several cross-linked epoxies in the glassy state. Tensile creep and tensile stress relaxation were measured during isothermal physical aging, following rapid quenching of samples annealed above the glass-transition temperature (Tg). The momentary creep curves measured at 21°C, 45°C, and 61°C below Tg for different epoxies could be fitted to an empirical equation for the creep compliance D(t): Values for β and to were obtained, and the dependence of to on the aging time was determined. Shift factors were calculated to investigate changes in molecular mobility during physical aging. The momentary stress relaxation was measured on the same epoxy materials as used for the creep studies. The stress relaxation curves were fitted to the following equation for the tensile modulus E(t): Values for α and to were obtained. The influence of physical aging on-to was again studied by calculating shift factors as a function of the aging time. The results are compared with the results of the creep tests and discussed in the context of current molecular theories of physical aging of glassy polymers.

Journal ArticleDOI
TL;DR: In this paper, rubber incorporation improves both impact and FCP resistance, but results in slightly lower Young's modulus and Tg As Tg increases, the degree of toughening decreases.
Abstract: Epoxies containing epoxy-terminated butadiene acrylonitrile rubber (ETBN) or amino-terminated butadiene acrylonitrile rubber (ATBN) were prepared and studied in terms of fatigue crack propagation (FCP) resistance and toughening mechanisms. Rubber incorporation improves both impact and FCP resistance, but results in slightly lower Young's modulus and Tg As Tg increases, the degree of toughening decreases. Rubber-induced shear yielding of the epoxy matrix is believed to be the dominant toughening mechanism. Decreasing fatigue resistance with increasing cyclic frequency is observed for both neat and rubber-toughened epoxies. This result may be explained by the inability of these materials to undergo possible beneficial effects of hysteretic heating. FCP resistance is linearly proportional to Mc1/2, where Mc is the apparent molecular weight between crosslinks determined on the rubber-toughened material. FCP resistance also increases with increasing static fracture toughness KIC. ATBN-toughened epoxies demonstrated better fatigue resistance than ETBN-toughened systems.

Journal ArticleDOI
TL;DR: In this paper, the impact fracture energy (Gc) for polypropylene homopolymer and a copolymer with and without calcium carbonate fillers was measured over a range of temperatures between −40°C and 40°C using fracture mechanics principles.
Abstract: The impact fracture energy (Gc) for a polypropylene homopolymer and a copolymer with and without calcium carbonate fillers was measured over a range of temperatures between −40°C and 40°C using fracture mechanics principles. The fillers studied were Omyacarb (∼2.7 μm) and Winnofil (∼75 nm) and 10% by weight was added to the matrix material. These fillers did not have any appreciable effect on Gc of the copolymer-based composites. However, the Omyacarb fillers improved Gc of the homopolymer at low temperatures (⩽20°C) due to enhanced microplastic flow as observed on the fracture surfaces. The fillers increased the stiffness of both the homopolymer and copolymer. It would appear that up to 10% of cheap calcium carbonate fillers could be added to the more expensive polypropylene to reduce the production cost without any significant loss of impact fracture energy.

Journal ArticleDOI
TL;DR: In this article, the authors applied transparent dimethyl siloxane network polymers with refractive indices near 1.40 to fused silica fibers to produce plastic-clad silica optical fibers.
Abstract: Transparent dimethyl siloxane network polymers with refractive indices near 1.40 may be applied to fused silica fibers (n = 1.458) as they are drawn to produce plastic-clad silica (PCS) optical fibers. The evanescent tail of the light energy propagating in the core of such fibers extends into the silicone cladding, where it interacts with chemical species present in the polymer. If the silicone is doped with a dye, the absorption spectrum or fluorescence spectrum of the dye is reflected in the transmission spectrum of the fiber. Further, if the dye changes its absorption spectrum or fluorescence spectrum as a result of diffusion of a chemical species into the silicone, the change is detectable in the fiber output. The polymer material properties which determine the performance of these sensors are described, along with examples of sensors for ammonia and oxygen which utilize either color changing or fluorescent dyes.

Journal ArticleDOI
TL;DR: In this paper, the prevailing mixing mechanisms of various screw elements employed in co-rotating twin screw extrusion process, including regular flighted, and reverse and forward kneading disc elements, were experimentally investigated.
Abstract: Co-rotating twin screw extruders are widely used for various mixing and reactive extrusion tasks in polymer processing operations In this study, the prevailing mixing mechanisms of various screw elements employed in co-rotating twin screw extrusion process, including regular flighted, and reverse and forward kneading disc elements, were experimentally investigated A direct goodness of mixing technique based on pigmented thermoplastic elastomers and computerized image analysis was used The results were elucidated in conjunction with mixing indices suitable for image analysis and the continuous mixing process Significant differences in the distributive mixing characteristics of various screw elements were revealed

Journal ArticleDOI
TL;DR: In this article, the authors used an isothermal weight-loss method to obtain the Arrhenius parameters of the thermal decomposition of poly(aryl-ether,ether-ketone) (PEEK) in a nitrogen atmosphere.
Abstract: The kinetic parameters of the thermal decomposition of poly(aryl-ether-ether-ketone) (PEEK) in a nitrogen atmosphere have been obtained using an isothermal weight-loss method. Several mathematical approaches have been used to obtain the Arrhenius parameters based upon the use of different reaction models. The values obtained for the activation energy (E = 198.4 to 219.7 kJ/mol) and preexponential factor (log A = 11.1 to 12.3 min−1) fall within a narrow range, irrespective of the method of calculation. Although the kinetic data most closely fits an Avrami two-dimensional nucleating model, the data can be just as easily described by a first-order rate law.

Journal ArticleDOI
TL;DR: Preparation de copolymeres segmentes siloxane/imide par reaction d'α,ω bis-propylamino oligo(dimethylsiloxane) avec un dianhydride organique (pyromellitique, phtalique, chloroformyl ph talique) in presence d'une diamine as mentioned in this paper.
Abstract: Preparation de copolymeres segmentes siloxane/imide par reaction d'α,ω bis-propylamino oligo(dimethylsiloxane) avec un dianhydride organique (pyromellitique, phtalique, chloroformyl phtalique) en presence d'une diamine. Les polymeres obtenus presentent, selon leur composition, des proprietes de caoutchouc thermoplastique, un caractere hydrophobe, une permeabilite elevee aux gaz, une bonne stabilite aux UV et une resistance a un plasma a oxygene