ALBERT

Notes: Studies of polypropylene oxyluminescence show the luminous intensity to be dependent upon the degre of oxidation. The length of the low intensity level portion of the luninescence curve, or pseudo induction period, was found to be a measure of the useful stabilizer life, and the intensity of this portion indicative of the effectiveness of stabilization. The effect of peroxide decomposers was studied and results indicate that peroxide reactions are major producers of luminescence. Analysis of the accepted modes of polymer oxidation, in view of our luminescence findings, indicate that the rate of luminescence buildup should depend upon ease of R. formation and the luminous intensity should be dependent on peroxy radical concentration. The effect of tertiary-carbon content on luminescence was also investigated, and luminous intensity was found to be dependent upon the amount of polymer branching. Model Compounds having slight structural variations were examined and were found to produce different intensity-time curves during oxidation, which may be attributed to ease of formation of a reactive site and subsequent peroxy radical reactions.

Notes: Sixteen polymers containing thiazole and aromatic rings in the polymer chain were prepared and investigated for the production of fibers and films that would be useful up to about 500°C. None of these polymers was completely satisfactory. Some of the polymers gave tough fibers and films, but they had relatively low melting points (〈300°C). Other polymers did not melt below 500°C, but they did not have good fiber and film forming properties because of their low molecular weights. Fibers and films of one of the polymers (polytetramethylenephenylenethiazole) were prepared, and their physical properties, hydrolytic stabilites under acid and alkaline conditions, and resistence to ultraviolet and gamma radiations were determined.

Notes: This paper is an account of some studies of the mechanism of degradation of an uncrosslinked polyurethan prepared from poly(propylene oxide) (PPO) and 2,4-tolylene diisocyanate (TDI) at temperatures up to 320°C in a vacuum or inert atmosphere. Fractionation of polymers before and after degradation provides information about the mechanism of degradation since the molecular weight distributions obtained are dependent on the mode and sites of bond scission. A recent publication describes the column elution method of fractionation developed for undergraded and slightly degraded PPG-TDI. PPO-TDI gives essentially most probable molecular weight distributions at an initial intrinsic viscosity [η] of ∼ 0.68 dl/g and also after degradation to [η] ∼ 0.24 dl/g. This invariancy of the distribution strongly suggests a randon scission process. Other types of degradation, e.g., free-radical unzipping initiated at the chain ends, could also give invariant most probable distributions. However, such depolymerizations would be accompanied by much larger extents of volatilization than were observed for these polymers (〈5% volatilization).

Notes: Moisture present in epoxy anhyride composites may hydrolyze the anhydride and cause major changes in the mechanical and chemical properties of the final composite. Heat distortion data and infrared spectroscopy are used to analyze the changes caused by the presence of the moisture. As the concentraton of water is increased, there is a decrease in the heat distortion or gass transition temperature. The decrease is due to a change in the crosslinking network and is caused by the reduction of the functonality of the epoxy group for acid as compared to the anhydride. Where rigid specifications must be met it is essential that the moisture level in the fillers, resins, etc. be kept constant.

Notes: There is considerable literature on the behavior of polyethylene below 200°C and above 400°C. This paper presents results on both high and low density polyethylene between 2000 and 400°C, a range of practical import for various fabrication and processing steps. Practical exposure times may be short and the experimental procedures were designed to give meaningful results for times as low as 1 min. The principal effects are chain-session and oxidation. Session was isolated by applying an atmosphere of pure nitrogen and proved uite shlow at 300°C but rapid at 400°C. The course of scission and produces discoloration, odor, and rising carbonyl content. A brief discussion is given of the role of diffusion in oxidation.

Notes: The application of silane coupling action produces significant improvements in physical properties in various thermpolastic resin systems. Both glass-reinforced thermoplastics and the more conventional filled thermoplastic resin systems were studied. An order of specificity between resin and coupling agent exists for thermoplastic resins similar to that of thermosets. The interaction with thermosets is considered copolymerization, wereas that with thermoplastics is not yet clearly defined. The silanes are incorporated by pre-treatment (best for glass reinforcement) or by addition during normal compounding. Fillers are added for a specific result, often with sacrifice of physical strength. Data presented show that silane addition upgrades filled thermoplastics to the level of clear resins and sometimes above. The effect of silanes on electrical properties of filled thermoplastics are also reported.

Notes: An optical method has been developed to provide quantitative results useful for characterizing the crazing of transparent plastics. The procedure consists of the detection of discontinuities in a beam of light that scans the specimen in a direction perpendicular to the line of crazing. The light is transmitted to a photomultiplier that is connected with an amplifying system and a recorder that provides a diagram of the light energy modulated by the lines of crazing. The specimen is scanner both before and after subjecting it to a treatment that causes crazing, and the crazing index is considered to be the difference between the area below the two curves.

Notes: Many rigid PVC compounds show a sharp transition from tough to brittle fracture with decreasing temperature in impact testing, and this temperature becomes a criterion of compound quality in addition to the impact strength observed at specific temperatures. This BT (brittle fracture) has been investigated individuall in commercial and experimental elastomer modified rigid PVC compounds. Factors affecting the BT include speciman thickness, composition and processing conditions. Apparently the discontinuity in impact behavior is a sudden manifestation of a gradual change, resulting in a near ten-fold decrease in notched impact strength without any obvious change in properties. The BT provides a continuous scale for comparing impact properties of compounds, and is thus more versatile and sensitive than impact tests run at a single temperature.

Notes: The flow of polymer melts is normally laminar, but pseudoplastic in character. That is, flow rate increases in proportion to a power higher then 1, usually between 1.5 and 4, of the applied pressure difference. Viscosities are extremely high - more then a mollion times that of water - so considerable heat is generated in the flowing melt by viscous dissipation of flow energy. This mode of heat generation is put to good practial use in the screw extruder, a device that converts plastic pellets into hot melt for shaping into pipe, sheets, coatings and molded products. Equations are given for computing flow rates and viscous dissipation rates. Heating (except by viscous working) and cooling of polymers are slow processes because all these materials are poor heat conducts nad their extreme viscosities make convection impracticable. The princliples of heat transfer are reviewed, and the solutions are given for some transient-conduction problems frequenlty encountered in processing. Equations are given for judging the operation of extruders.

Notes: Tangential flow of a “power law” model fluid between two concentric cylinders is analyzed. A constant angular pressure gradient is imposed and one of the cylinders is rotating at a constant angular velocity. This type of flow is of interest in screw extrusion theory. The error in the superposition, i.e., linear addition of tangential pressure and drag flows, for a “power law” model fluid, is quantitatively calculated and plotted in the form of a correction factor. Tangential pressure flow is compared to a pressure flow between parallel plates and additional correction factor to account for the curvature is derived and plotted. The applicability of the “power law” model for flow of polymer melts in extruders is also discussed.

Notes: This article describes a general mathematical model summarized in the form of a computer program for the plasticating extruder. The model combines features of the metering-zone model previously published, the melting-zone model described in paper No. I of this series, and a feed-zone model based on an extension of known theories. It is based on theoretical models for each zone unified and improved by non-linear estimation to accurately describe the extrusion experiments.The mathematical model predicts temperature, pressure, and melt channel width profiles of the plastic being processed in the plasticating extruder as a function of design and operating variables of the machine. It enables for the first time the design of the whole machine based on temperature and pressure profiles, including new combinations of cylindrical and tapered roots.

Notes: The development of a fractional crystallization technique for characterization of polypropylenes with respect to stereoregularity is described. It is a simple technique which is attractive for routine analysis and under suitable conditions yields quantitative data with good reproducibility. Separation by fractional crystallization from hot xylene solution is shown to take place according to polymer crystallizability and is relatively independent of molecular weight. It thus represents an alternative and in some ways superior approach to the more commonly used fractional extraction method. Preliminary work indicates that the fractional crystallization method may prove of value in establishing correlations between the stereoregular nature of polypropylenes and their physical properties.

Notes: The density and tensile property changes in polypropylene resulting from various post-crystallization aging procedures are investigated with the aim of (1) establishing standard procedures for the evaluation of these properties and (2) determining which conditioning treatment will provide optimum tensile properties. The morphology and resultant tensile behavior of polypropylene are particularly sensitive to conditioning treatments in the temperature range 145-160°C. A procedure for compression molding plaques, carrying out isothermal annealing treatment in the 100-170°C range and gradual cooling is described. The dependence on annealing temperature of the density, elongation, tensile modulus and yield stress is given.

Notes: Some earlier observations on the influence of molecular weight, plasticizer, and irradiation on the thermal conductivity of polymers is reviewed. Also some new data on polystyrene and some new calculations based on the theory of Hansen and Ho are presented. These data show almost a two fold increase in the thermal conductivity of polystyrene as the molecular weight goes from 900 to 100,000. Data on the moleculer weight effect on thermal conductivity appear to be consistent with the theoretical calculations.

Notes: Thermal oxidation in linear polyethylene is mainly confined to disordered regions in which scission reactions cause crystallization and eventual deterioration of mechanical properties. Gel formation is negligible at 100°C. As degradation proceeds, comparable changes occur in the intrinsic viscosities of melt and solution-crystallized liner polymers, indicating that chain folds are regularly arranged and are resistant to oxidative scission. Breakdown is much more extensive in branched and crosslinked polymers since crosslinking retards oxidative crystallization and branching increases the volume fraction of substrate ultimately accessible to oxygen.

Notes: For a system of equivalent bonds undergoing random bond scission it is reasonable to assume that the rate of bond breaking (hence the rate of creation of new molecules) reported in the literature and data presented here demonstrate that the number of molecules created is not proportional to the time of thermal treatment hence they seem to belie this reasonable hypothesis. Other authors have adduced the presence of some non-equivalent bonds in order to account for the observed cruvature and still retain the hypothesis. Implicit in these arguments is the assumption of a steady-state concentration of reactive fragments. Our analysis explores the consequences of abandoning the steady-state assumption and shows that a quantitative explanation of the observed degradation behavior may be had by this means wihile still retaining the hypothesis of a constant probability of a bond being broken per unit time.

Notes: Most polymers exhibit a very fluid melt rheology during extrusion and can be distorted, drawn down, and cooled without building excessive residual stresses into the product. In contrast, rigid vinyl is usually extruded as a stiff, almost selfsupporting mass. Care must be taken to prevent the formation ot oriented stresses in the product which will be relieved during long periods of exposure resulting in dimensional instability and related loss of physical properties. A newly developed method of in-line annealing has shown to be an effective means of relieving oriented stresses developed during extrusion. By use of this instrumented technique, rigid vinyl products can be controlled to much tighter shrinkage specifications in a single step process, thereby eliminating post-annealing treatments.

Notes: Residence time distribution (RTD) is a spectral property of contiuous chemical reactors. Batch reactors may be viewed as having “monodisperse” residence time distributions. This article discusses molecular weight distributions (MWDs) of polymeic materials formed in continuous and in semicontinuos process and how they are affected by reaction time distributions. All synthetic high polymers, even those Prepared in batch reaction, possess a MWD which may sometimes, for a given monomer, be altered chemically by a proper choice of catalyst and diluent. An interesting concept suggested by the present work is the prospect of “tailoring” the MWD for a given monomer-catalyst-diluent system physically by selecting appropriate reactor conditions. Hence, althought this work involves analysis the results may provide a guide to synthesis.

Notes: Commercial films, elastomers, and fibers have valuable in-use properties below 300°C. Astronautic requirements, however, may evaentually call for materials that withstand 500 hrs at 300°C or 100 hrs at 500°C while fully retaining their useful properties. The most significant advances in the synthesis and preparation of heat resistant polymer have been made since 1959 with new synthetic methods such as interfacial polymerization, cyclopolymerization, and intramolecular polymer post-cyclopolymerization, and intramolecular olymer post-cyclization reactions. It is the purpose of this paper to discuss the structural relationships among those heat resistant, orgainc polymers that were reported to give strong films and fibers. Those heat resistant polymers, which have not yet been fabricated into films and fibers are not included in this review.

Notes: Monodisperse and polydisperse polystyrenes of equal weight average molecular weight (Mw) are evaluated for melt flow behavior in an Instron capillary rheometer and for injection molding behavior in a 12 ounce in-line reciprocationg screw injection molding machine. The influence of molecular weight distribution on the shape of the flow curves is deconstrated over a wide range of shear rate and temperature. The influence is also reflected in injection molding behavior as defined by pressure to fill or flash the mold at a given melt temperature. Studies of capillary rheometer data for correlation with injection moling beghavior indicate poor agreement when low shear rate viscosity data are used. Good agrement is foun using high shear rate viscosity data in the range 103 to 104 sec-1 Striking crossover points on melt rheology and injection colding area diagram curvs are found with the monodisperse and polydisperse polystyrenes of the same M These crossovers shift with melt temperature and make possible the determination of a “controlling shear rate” for the injection molding process. This is found to be 3500 sec-1 for short shot and 6200 sec-1 for flash with the ASTM test specimen mold used in this study.

Notes: The stress-strain characteristic of polymeric binders and solid propellants are dependent on the crosslink density, molecular weight between crosslinks, molecular weight distribution in the binder formulation, volume fraction of filler, and the interaction between the binder and filler particles. This investigation is directed toward elucidation of solid propellant microscopic response and failure mechanisms through characterization of the constitutive effects of crosslink density, molecular weight distribution and curing agent ratio in the binder formulation, and filler fraction. This was accomplished on the ERLA/PBAA propellant system through investigation of three binder formulations with the same curing agent ratio but different crosslink densities; five binder formulations with different curing agent ratios; and four formulations with up to 69.9% by volume of filler.Uniaxial stress-strain characteristics were determined on each formulation at displacement rates of 0.2 to 20.0 in/min at isothermal test conditions ranging from 75 to -90°F. The failure characteristics of a viscoelastic material represent a curve in the three-dimensional space of stress, strain, and time. The ultimate property data on each formulation are presented as projections of this failure curve on the stress-strain, stress-time, and strain-time planes, respectively. Relationships are developed for the dependence of the stress-time, strain-time, and stress-strain failure envelopes on the volume fraction of bound rubber, crosslink density, molecular weight distribution and curing agent ration in the binder component, and the volume fraction of filler.

Notes: Two independent methods for predicting the deformation of free openings of arbitrary shape in a viscoelastic plate are illustrated.The first method is experimental and is based on the interference of two systems of lines representing the initial and final positions of the material. To demonstrate the moire method, the creep compliance function for polymethylmethacrylate is determined as preliminary information. This function is used as input data in the ensuing theoretical analysis to insure realistic viscoelastic behavior.The second method involves techniques to approximate viscoelastic displacements from known elasticity solutions and known material properties.The methods are applied to two examples: (1) The square hole - to determine the motion of an opening of complicated shape; and (2) an ellipse loaded at 45° - to indicate qualitative agreement with an existing prediction of the motion of cracks in a viscous plate.

Notes: A simple, versatile biconical rehemoter has been developed. This device provides shear creep and creep recovery data for polymer melts over a temperature range of 200-500°F. and a range of applied shear stresses from 2 × 103 to 9 × 105 dynes/cm2.Extensive reheological data have been obtained for two samples each of polyisobutylene and high-density polyethylene. These illustrate the value of the device in obtaining data useful for predicting and understanding the processing properties of polymer melts.

Notes: Considerable progress has been made in the past 20 years in the synthesis, characterization and fabrication of plastics. Previous SPE Award winners, such as Mark, Natta, and Marvel dealt largely with synthesis; Flory with characterization; Alfrey and Du Bois with fabrication. One of the still unsolved problems lies in the realm of relating mechanical properties, such as impact strenght and creep to molecular structure.The design enginner who wishes to use a plastic part is concerned primarily with how some property such as impact strenght varies with temperature, speed of test, test method, etc. The polymer scientist must know why. Through knowing why, he may be able to design better plastics.This paper attempts to survey some of the world-wide progress made in this area in the past 10 years. The ultimate goal is to understand these mechanical properties in terms of internal molecular motions which occur in solid polymers. Internal motion can be detected by electrical, electromagnetic and dynamic mechanical measurements. When these three methods are applied on a given polymer over a range of temperatures, insights can be gained as to the variation of impact strength and other properties with temperature and frequency for that same polymer. These three fundamental methods, which require very small samples (less than 50 grams), can provide insight into the practical behavior of plastic materials over the wide range of temperatures and frequencies encountered in the real world.

Notes: A knowledge of the variation of melt viscosity of thermoplastic polymers with both shear rate and temperature is of considerable importance to plastics engineers as well as to polymer rheologists. The actual measurement of melt viscosity at a large number of temperatures and shear rates is frequently a tedious and time-consuming task. A technique has been developed, based upon the applicability of shear rate-temperature superposition, for predicting the flow curves of a number of olefin polymers and copolymers at various temperatures from experimental data obtained at one temperature for the material in question. The experimental validity for superimposing log shear stress - log shear rate curves at different temperatures along the log shear rate axis has been established for both high and low density polyethylenes, polypropylene, polybutene-1, and poly (ethylene vinyl acetate) copolymers. The temperature dependence of the resultant shift factors has been determined for each system, and the method of utilizing this information to predict viscosities as a function of temperature and shear rate is discussed.

Notes: A dynamic mechanical study has been made of an ethylenemethacrylic acid copolymer containing 4.1 mole per cent of methacrylic acid units and its sodium, lithium and calcium salts. On the basis of the results and related physical chemical studies it is proposed that the structures of the ionized copolymers consist of three distinct phases - a crystalline polyethylene phase, an amorphous polyethylene phase, and an ionic phase consisting of ionic domains. It is further proposed that the unionized acid copolymer consists of two phases - a crystalline polyethylene phase and an amorphous phase consisting of polyethylene crosslined with hydrogen bonded, carboxylic acid dimers.

Notes: The true stress-true strain behavior of polyoxymethylene, n(-CH2O), as an example of a bulk semi-crystalline polymer, has been investigated for constant hydrostatic environmental pressures from 1 atmosphere to 8 kilobars with the principal objectives of elucidating the factors controlling flow and fracture. Experiments were conducted in uniaxial tension at room temperature and constant strain rate. The tensile observations were supplemented by measurements of bulk compressibility and stress relaxation behavior at pressure.In contrast with metals and inorganic compounds, the modulus, yield stress and fracture stress of POM increase strongly with pressure by a factor of approximately three at 8 kilobars. The modulus increase is shown from the stress relaxation measurements to be associated with a pressure-induced increase in the β-transition temperature which points to the potential usefulness of the concept of pressure-temperature super-position of mechanical behavior. The characteristics of the pressure dependence of the yield stress demonstrate that yield criteria based on continum mechanics considerations, including the Mohr or Coulomb-Navier criterion, are not valid for general deformation (non-plane strain) conditions in this polymer. The concept of a critical volume change determining the initiation of yielding is suggested to be applicable to semi-crystalline polymers. Comparison with analogous changes in yield stress with temperature points to an increasing contribution to the control of yielding by the initially disordered regions with increasing pressure or decreasing temperature. The fracture behavior observed at pressure eliminates the concepts of a critical stress as a fracture criterion for POM and of a simple reduction in normal stress at points of stress concentration as the principal effect of the applied pressure on fracture.

Notes: This investigation considers a hypothetical three-phase ordered composite to permit the design of a new material both stiffer and tougher than the matrix phase alone. The required elastic solution is greatly simplified and was based on a single layered inclusion in an otherwise infinite matrix under uniaxial tension. The solution presented is exact and generalized to accommodate any number of concentric layers of different thickness and composition.

Notes: Attempts to use low-cycle fatigue techniques derived from the work of Coffin and Manson to predict the fatigue performance of six diverse structural plastics are discussed. Through an analysis of dynamic property and thermal behavior studies of polymer samples in reversed-tension fatigue, an improved model for the polymer fatigue process has been proposed. Laboratory test data are presented illustrating the relationship between the various models.

Notes: It is postulated that property gradients exist at the interface forming an “interphase” between the insert and the matrix. Such gradients might be caused by partial solubility and diffusivity of the two phases comprising a composite. For simplicity, the “interphase” is replaced by a shell exhibiting averaged properties (Eshell = 1/2 Einsert + 1/2 Ematrix, etc.). An exact linear elastic solution was employed to evaluate stress fields throughout all regions. The possible effect of the “interphase” and its thickness on several physical properties of the composite are evaluated in terms of the particular stress fields.

Notes: An investigation of the dynamic mechanical properties of several molten polymers was performed using the Maxwell Orthogonal Rheometer. Relaxation spectra derived from experimental data for the terminal region of viscoelastic response indicate that as molecular weight distribution broadens, terminal relaxation phenomena associated with molecular disentanglement and translation extend over a corresponding wider frequency range. The same data indicate that a true maximum relaxation time beyond which no elastic response is observed exists for the materials studied. Moreover, the maximum relaxation time corresponds to the reciprocal of the frequency where the dynamic viscosity deviates from its zero-shear value. Thus an estimate of the time necessary for complete elastic recovery in polymer melts is readily obtained experimentally.

Notes: Tensile creep measurements were carried out on a commercial ABS polymer over a temperature range from 40 to 100°C at stress levels from 0.6 to 1.8 × 108 dynes/cm2. Experiments were conducted in a prototype of an apparatus designed to be compatible with digital acquisition systems. Analysis of the data indicated that application of the time-temperature super-position principle was of limited value due to the use of test temperatures near and below the effective glass transition temperature of the acrylonitrile-styrene component of the polymer. A strong stress dependence of the compliance was observed, even at relatively short times after loading. This was analyzed in terms of a model in which the height of the potential energy barrier to motion of the molecular flow unit is lowered by the application of stress. Analysis of the temperature dependence of the compliance at low stress levels indicated that the effective Tg of the acrylonitrile-styrene phase is about 85°C. The temperature dependence of the magnitude of the activation energy is considered as is the stress dependence of the glass transition temperature. Implications of short-time response in creep with regard to response under impact loading are pointed out. Practical application of results to the prediction of dimensional stability of molded parts is discussed as well as the limitations involved in extrapolation of experimental data to long times and high stress levels.

Notes: Fine structures of several plastic/rubber two -phase polymer systems were studied by means of direct observations of ultrathin sections under the electron microscope using osmium tetroxide staining and a hardening procedure developed recently by Kato. Samples used are several types of both ABS polymers and high -impact polystyrenes, and several PVC/rubber blends and the results were discussed in relation to their dynamic viscoelastic properties. It is suggested that these studies may fruitfully be extended to clarify the structure -to property relationships by use of this method.

Notes: The purpose of this paper is to describe a new deformation calorimeter, which is based on differential thermometry and uses a flowing gas stream as a heat transfer medium which allows it to operate under near-isothermal conditions. Also presented are some preliminary test measurements with a crosslinked polyurethane elastomer and crystalline polybutene-1.

Notes: Antiplasticizers are considered to be diluents which when added to polymers result in mechanical property behavior opposite to that of plasticization. The addition of antiplasticizers to certain polymers such as Bisphenol A polycarbonate, polysulfone, and polyvinyl chloride results in the elimination of the secondary loss transitions of these polymers. As a drop in modulus accompanies these transitions, their elimination results in higher tensile strength and tensile modulus. As secondary transitions are commonly associated with ductility and impact strength, their elimination also results in the observed embrittlement characteristics. The addition of anti-plasticizers to polymers also restricts the diffusion of penetrants resulting from the decrease of molecular flexibility in the polymer matrix.

Notes: A useful concept in polymer science is the degree of crystallinity - the fraction of the polymer that exists in a relatively ordered state. Methods of determination of the degree of crystallinity using density, infrared, thermal, N.M.R. and X-ray measurements are examined in light of modern notions of the structure of semi-crystalline polymers.

Notes: The changes occurring when polythene melts are subjected to shear, have been investigated using a rotating bob fitted into a ram extruder. In addition to chain scission, low density polythene exhibits reversible changes in mechanical and viscoelastic properties. The magnitude of the changes is controlled by total shear strain, and is related to molecular weight and long chain branching. The mechanism appears to be one of reversible disentanglement operating mainly on the large highly branched molecules. The work is relevant to various extrusion processes and to other long-branched polymers.

Notes: This investigation deals with the fatigue behavior of a group of thermoplastics fortified with discontinuous glass fibers dispersed by an injection molding process. The thermoplastics included nylon, polystyrene and polyethylene reinforced with short (1/8 in.) and long (1/2 in.) glass fibers.Several aspects of the fatigue behavior are included in the study. First, classical S-N curves were generated under fluctuating tension with R = 0.05 to show the loss of strength due to cyclic load application. Next, the extent of progressive fatigue damage was established by measuring the residual strength after cyclic loading. Finally, hypotheses pertaining to the fatigue mechanisms operative in all four materials were made based on microscopic examinations of sections removed from fatiguedamaged specimens.

Notes: More than seventy materials were examined for their ability to improve the performance of DTDP plasticized PVC wire formulation in a modified 105°C wire oven aging test. Twenty of these were as effective as the widely used Bisphenol A, four of which were effective at a lower concentration.

Notes: Extrapolation from data on low molecular weight n-alkanes indicates that the surface tension of polyethylene at 150°C is 26 dynes/cm. The total surface energy, γ  -  Tdγ/dT, is 51 dynes/cm and is much less dependent on chain length. The surface tension of polyethylene extrapolated to 20°C is 34 dynes/cm, consistent with the critical surface tension below which liquids will wet the polymer. The total surface energy is in reasonable accord with the incremental energy of vaporization, 1.029 kcal/mole of CH2 groups. The surface entropy is less than that of low molecular substances. This is attributed to a reduction in the opportunities for rotational isomerism at the surface.

Notes: A first order transition was observed in the temperature range of about 210°C by dilatometric studies on both isotactic and atactic polypropylene and for isotactic poly (butene-1) and poly (pentene-1). No such transition was observed for polyethylene. It was found that the transition is not due to the measurements per se, to polymer treatment, to catalyst residues, or to polymer degradation. It is suggested that the transition could be due to the disappearance of liquid crystals.

Notes: The melt viscosities of three low density polyethylenes of widely varying melt indices were studied as a function of temperature over a broad range of shear rates and shear stresses. Apparent viscosities at constant shear stress could be fitted adequately to a simple Arrhenius equation over the entire temperature range studied. However, pronounced curvature of the log ηa-1/T curves was observed for apparent viscosities at constant shear rate. The apparent activation energies for viscous flow at constant shear stress were found to decrease slowly with increasing shear stress and also to decrease with decreasing molecular weight. A temperature-shear rate superposition was demonstrated to hold, and the shift factor dependence on temperature was determined.

Notes: Thermal conductivity curves for the 0°C to 170°C temperature region are presented for six irradiated low density polyethylene samples (radiation doses from 0 to 3100 megarads) and one irradiated high density sample (120 megarad dose). In agreement with data in the literature for unirradiated polyethylene, the thermal conductivity values for lightly irradiated polyethylene are found to decrease with increasing temperature in the elevated temperature region where the crystallites begin to melt. Beyond the crystalline melting point, test results for lightly irradiated and crosslinked samples indicate that the thermal conductivity is almost independent of temperature. Although radiation doses of less than 250 megarads produce only small changes in the thermal conductivity, higher radiation doses result in a significant lowering of the conductivity in the room temperature region and an increase of the conductivity at temperatures above the melting point. The decrease in conductivity at low temperatures is considered to be a result of disordering of the crystallites by the radiation, and the increase above the melting point is attributed primarily to radiation induced crosslinking.

Notes: Unsaturated polymers thermally degrade by a number of different mechanisms depending on the structure of the polymer and the experimental conditions. By use of deuterium tagging it was shown that polyisobutylene degrades stepwise from the end by a cyclic unimolecular mechanism. Volatile products from isotactic polypropylene contained 75% propane at 340°, 64% n-pentane at 375° and 49% propylene plus 12% isobutylene at 495°. Polyethylene was shown to give mostly propylene at lower temperatures but gave a 60% yield of ethylene at 600°.

Notes: Recent studies of the morphology of semicrystalline polymers have demonstrated the inadequacy of the familiar fringed micelle concept. It is now generally recognized that polyolefins crystallize in a spherulitic form having a skeletal structure of coherent crystals with a fibrous habit. Crystallization occurs in two stages: (1) spherulitic growth of crystalline lamellae, and (2) partial crystallization of residual melt in regions between lamellae. The dependence of modulus on degree of crystallinity in polyethylene indicates that the crystalline network carries much of the elastic energy acquired when the plastic is subjected to stress. Two of the mechanical transitions are also related to morphological structure. The high temperature or α transition is attributed to motion within lamellae while the intermediate or β transition is attributed to motion in disordered regions between lamellae.

Notes: Many plastic articles when exposed outdoors deteriorate first at points of highest stress. Consequently, weathering of polyolefins under stress speeds the deterioration and hence the evaluation of ultraviolet stabilizers used to retard it. Cracking of the stressed polyolefin specimens denotes failure and is a direct measure of the minimum useful outdoor lifetime of the materials, whereas in other methods the change in some property, such as elongation, is used to predict the useful lifetime. In this work, the results of nine years of natural and artificial weathering illustrate the usefulness of the stresscracking method for evaluating polyethylene and polypropylene compositions. The evaluation of compositions by this method was found to correlate with that made by measuring the loss of elongation during outdoor weathering.

Notes: Fracture surfaces record the kinetics of failure at two levels in the structure of polymeric solids. The first is evidenced by the formation of geometric markings resulting from the interaction of the primary fracture front with secondary fractures developing radially just ahead of the primary fracture. These markings are often visible to the unaided eye and have minimal dimensions in the micron range. The second fracture phenomenon appears to involve the orientation of molecular chains or bundles. Such orientation manifests itself in the interference-color producing film found on the fracture surfaces of poly (methylmethacrylate) and polystyrene. It is also apparent in the free or adherent film found on the surfaces of large fractured crazes. Some evidence is presented for the existence in these films of chain bundles 30A or less in diameter. It would seem that similar mechanisms are operating in the production of “craze matter” and of fracture surface films.

Notes: This article presents data on outdoor weathering of unfilled epoxy resins. The data have been accumulated after five years of weathering. The anhydride cured epoxy resin system was least affected by outdoor exposure. In addition, systems with higher deflection temperatures were more resistant to attack by outdoor exposure than those of lower deflection temperatures. It was also evident that heat curing is better than curing at room temperature. Hardness, for all systems, decreased with exposure time. Microscopic examination of the exposed systems showed that surface change closely correlated with changes obtained in the mechanical and electrical properties tested in this program. Systems showing the greatest change also had the worst surface appearance.

Notes: There has been a marked increase in the interest shown in the field of characterization of polymeric materials via dynamic techniques, so much so that symposia devoted exclusively to “dynamic” properties of materials are now commonplace (1, 2). This article provides both a frame of reference with regard to the wide variety of “dynamic” test techniques now in use, and…as well…dynamic test data for a wide range of polymers. Particular emphasis will be placed upon the difference in function of varying test techniques and the applicability of data obtained for specific R & D vs engineering applications. For the purposes of the presentation an arbitrary distinction will be made between “dynamic” tests of the cyclic type and “dynamic” tests of the unidirectional type.

Notes: The balance of engineering properties of rubber-modified polystyrene make it attractive for many applications, but it is difficult for the design engineer to relate laboratory data to service requirements because of differences in strain rates, temperatures, etc. Data are presented which show how the toughness and stiffness of an appliance-grade, impact polystyrene vary with impact velocity (or loading rate), temperature, fabrication method, and pigment level. The ability to survive multi-axial impact loads is strongly dependent on loading rate; a maximum in energy-absorbing ability was observed in the range 500-2000 in./in./min, where the failure mechanism changed from ductile to brittle.

Notes: The authors previously reported work on the kinetics and mechanism of the uncatalyzed thermal oxidation of isotactic polypropylene. The data, obtained form infrared absorption spectra of the carbonyl region, was utilized in developing the theoretical expressions presented. This paper summarizes this work and presents further evidence which substantiates the derived expressions. The additional evidence is obtained from infrared absorption spectra involving the apparent hydroperoxy region and from measurements on the rate of formation of volatile products. Some recent pertinent literature is also discussed.

Notes: The time-dependent mechanical behavior of solid polymers can be classified into linear viscoelastic, nonlinear viscoelastic and rheological types. The linear viscoelastic theory has now been worked out in detail, and applies with particular success to amorphous polymers above their glass transition temperature. Examples of systems falling outside this category are principally discussed, including glassy, composite, and crystalline materials. These systems are characterized by the fact that structure and structural changes are playing a major role in the mechanical behavior. Specific theories must be developed in the future which adequately treat this type of behavior.

Notes: The thermal degradation of polytetrafluoroethylene has been investigated in a closed system as a function of the nature of the surface of the reaction vessel wall. Reproducible results cannot be obtained in a stainless steel vessel as metal fluoride is continuously formed and a stable fluoride is not formed on the wall. Quartz spoon reaction vessels coated with calcium fluoride give a few reproducible runs, before the coating has to be renewed. If the dimerization of the monomer, which takes place very rapidly around 600°C, is considered, first order rates are obtained up to about 75% monomer formation. The kinetics is briefly discussed on the basis of random initiation followed by depropagation with a relatively short kinetic chain length and disproportionation as termination reaction.

Notes: There are essentially two ways to arrive at high softening polymers: crystallization and cross linking. The first approach leads to thermoplastic materials which have a more or less sharp and reversible melting point; the second produces three dimensional unmeltable networks which are thermosetting and can support very high temperatures without degradation. Factors which affect the mechanical behavior of a polymer exposed to high temperatures are degradation and cross linking. The first process is caused by scission of the chain molecules. The second process, cross linking, ties individual polymer chains into a rigid network, increases the molecular weight and leads to a very hard, brittle product which can neither be melted nor dissolved. The stability of a polymer against oxidation is always improved by the addition of an oxygen scavenger which reacts with oxygen in preference to the polymer and also by the addition of a UV absorber.

Notes: Creep experiments under combined tension and torsion loading are reported for tubular specimens of polyvinyl chloride copolymer. Experiments include a sequence of several combinations of tension and torsion on each specimen with abrupt changes between combinations, including reversal of sense of torsion, recovery and reloading after recovery.Results show a strong path and time dependence for the strain and for the direction of the strain-rate vector at constant state of stress following a change in state of biaxial stress.The character of the results is described reasonably well by the Boltzmann superposition principle of linear viscoelasticity using a constitutive equation of the form: Examples are given of the use of this equation for common states of stress.Better agreement with the data is obtained from a similar but non-linear equation employing hyperbolic sine functions of stress.

Notes: Liquid SO2 sealed into tubes made of a fluorocarbon copolymer permeates the walls of the tube at a temperature-dependent but accurately reproducible rate. Sulfur dioxide dispensers made in this way are called permeation tubes and are useful for calibrating instruments that measure SO2 concentrations in air. The National Bureau of Standards calibrates SO2 permeation tubes and makes them available as Standard Reference Materials. The permeation rate in a batch of nominally identical tubes varies enough that each Standard Reference Material tube must be individually calibrated. Changes in the length or radial dimensions of the tubes are much too small to explain most of this variation. An excellent (negative) correlation is found between the measured permeation rate and the density of the polymer (or weight per unit length). Since both the measured density and the permeation rate for this semi-crystalline polymer depend upon morphological factors, but in different ways, x-ray diffraction measurements of the thickness and orientation of the lamellar crystals were made and a mathematical model was set up to identify the morphological factors which can cause variations in the permeation rate.

Notes: A theory for roll coating of a fluid onto a moving sheet is developed utilizing the usual “lubrication approximations.” The effects of fluid and operating parameters on coating thickness and pressure distribution are determined for a Newtonian fluid, and for a purely viscous non-Newtonian fluid obeying the Power Law. The results for these cases are obtained analytically, and are rather straightforward.A viscoelastic fluid is considered, of a type which shows typical non-Newtonian shear behavior observed in polymer melts and solutions and which also exhibits normal stress behavior. Analytical solutions are not possible, but a perturbation method, using a viscoelastic perturbation parameter related to a Deborah number, yields an approximate solution. Only terms to first order in the perturbation parameter are given. Subject to that degree of approximation, the following conclusions are drawn: 1Non-Newtonian shear behavior reduces the pressure distribution, and increases the coating thickness.1Elasticity of the type usually observed in polymer solutions makes only a minor contribution to the roll-separating (load-carrying) force. The contribution is positive, but smaller than the corresponding negative contribution due to the non-Newtonian shear effects.1An increase in load-carrying capacity would require a different viscoelastic fluid than the type considered here - one that is essentially Newtonian in shear but, independently, capable of developing significant normal stresses.

Notes: There are two distinct solid conveying theories that can be applied to plasticating screw extruders. One is Darnell and Mol's theory based on a solid-to-solid friction model and the other is Chung's theory based on a viscous shearing model. The two theories predict very different solid conveying performances for a same set of conditions. In this paper, the maximum pressures that can be developed inside plasticating screw extruders by the solid conveying force are calculated using each of the two theories. Comparison of the results may shed some light on the applicability of each theory for a particular extrusion operation.

Notes: The mechanical properties of a propylene-ethylene copolymer resin depend strongly on the mold temperature employed during injection molding. Average spherulite size correlates well with most physical properties; good impact properties are related to small average size, and high heat distortion temperatures to large average size. Tensile specimens have three distinct regions when viewed through crossed polars. The outer region (Region 1) does not contain spherulites, but Regions 2 and 3 do. The largest spherulites are found in Region 3, the center of the specimen. Region 1 has a molecular weight higher than that of the other two regions.

Notes: During the last several years there has been considerable interest in the occurrence of structure in certain bulk polymers normally thought to be structurally homogeneous. Specifically, it has been proposed that polymers produced by emulsion polymerization may retain a particle structure in the bulk state. This has been demonstrated by both rheological measurements and by electron microscopy. In this work we show conclusively that at least part of the particle structure observed by electron microscopy for polystyrene is an intrinsic feature of the fracture surface and is in no way related to the history of the sample.

Notes: Twelve polymers and copolymers reinforced with random short glass fibers are used for the study of the strength -composition relationship. Six of these reinforced systems are new and have not been reported elsewhere. The effect of fiber volume fraction on tensile and flexural strengths is related to the Kelly and Tyson equation. For each composition the strengthening factor, F, is calculated and discussed with respect to the structure of the polymer. One factor pertaining to the actual performance of fiber glass, fiber efficiency, K, has been extrapolated for the fiber glass used for this study. The effects of fibers on toughness and the Izod notched impact strength are discussed. It is the impact strength ratio and not the toughness which is used to describe the net result of reinforcement.The deviations between the wet and the dry strengths are used to illustrate the effect of the fiber -matrix interfacial bond. A new parameter, Δθ, is introduced to describe the effect of structure on the fiber -matrix interface. The effect of water at the fiber -matrix interface is further demonstrated through the determination of dielectric constant and dissipation factor of the composite before and after water immersion. The rule of mixtures was found to apply to dry electrical properties of composites.

Notes: The effects of shear stress on the crystallization kinetics and morphology of linear polyethylene and polybutene-1 were studied with the aid of a specially designed apparatus. With this equipment, it was possible to heat a thin polymer sample between glass slides to a melt temperature, quench the sample to a crystallization temperature, and then deform the sample in shear by applying a constant load to one of the glass slides. During the deformation, the crystallization process was observed and photographed under a polarizing microscope. Also, the displacement of the glass slide was simultaneously recorded which made possible a determination of the shear strain as a function of time.The results demonstrate that two phenomena may occur in the initially supercooled polymer samples in response to the applied shear stress. In one case, the sample deformed until it fractured, generally exhibiting no evidene of crystallization; in the other, the sample deformed until an inflection point was reached after which the sample became rigid. This latter phenomenon was attributed to crystallization.At low shear stresses, the inflection point was associated with the growth of spherulites which simply became large enough to bridge the glass slides and prevent further deformation of the sample. This generally occurred prior to the completion of the radial growth of the lamellae.At high shear stresses, however, no evidence of crystallization was seen in the microscope until the inflection point was reached. At this point, birefringence was observed in the sample. The resulting structure generally could not be resolved in the microscope, thereby indicating very profuse nucleation.The results obtained clearly demonstrate that the application of a sufficiently high shear stress to an initially supercooled melt has a substantial effect on the rates of crystallization of both polyethylene and polybutene-1. This was shown most dramatically at temperatures close to the melting point, e.g., both polyethylene at 130°C and polybutene-1 at 113°C, which require over 104 sec to crystallize under quiescent conditions, crystallized at approximately 0.05 seconds.The application of a shear stress to a polymer melt is envisaged as resulting in molecular orientation. In accord with the theories of Flory, and Krigbaum and Roe, the associated decrease in entropy of the melt may be considered to increase the supercooling. Under high stresses at which large increases in supercooling result, crystallization occurs more rapidy at the high temperatures and with polymers of lower molecular weight. At low shear stresses, the influence of temperature and molecular weight on the crystallization kinetics is essentially the same as that obseved under quiescent conditions.Observations through the microscope have shown that the application of a shear stress to a polymer melt leads to large increases in the number of crystalline structures formed and to the formation of oriented morphologies. This latter phenomenon arises due to nucleation lines formed by impurities and spherulites in the deforming melt. The impurities and spherulites apparently cause a disturbance which is thought to result in a local increase in stress of the melt and, hence, a local increase in supercooling. Lamellae then nucleate on these lines and grow out radially.

Notes: Mold flows and melt viscosities of an incompatible bi-component EPDM and “Viton” fluoroelastormer system were examined. A marked reduction in the melt viscosities of either component was observed when a small amount of the other component was present. It was speculated that the phenomenon was a result of a slippage between the polymer and the coated capillary surface due to the presence of a minor amount of the incompatible polymer. Evidence is given to indicate that this effect cannot be accounted for using the “melt structural heterogeneity” mechanism proposed for a different system by Andtrianova.

Notes: The Part I paper described the mechanochemical basis for achieving high adhesive strength in bonds between polymeric surfaces such as polyethylene, polypropylene, and Teflon, using the SABRA method (Surface Activation Beneath Reactive Adhesives). This paper gives a brief survey of bonding techniques as well as results of shear tests of simple lap joints and scarfed tube joints. They compared favorably with other methods such as CASING, Peeling test results are also presented. Mixed systems were examined such as glass fiber reinforced polyester bonded to polypropylene and aluminum with thin films of polymeric material sandwiched between. A start was made towards of optimization and exploration of primer specificity for different materials, The implications and further applications of the SABRA method are discussed.

Notes: Various blends over extended compositional ranges have beer, prepared for combinations of a thermoplastic urethane elastomer with polystyrene, a styrene-acrylonitrile copolymer, a polyhydroxyether (Phenoxy A), and poly(vinyl ethyl ether). The thermoplastic urethane elastomer was based on a polycaprolactone diol of approximately 2100 number average molecular weight, 4,4′-diphenylmethane diisocyanate and 1,4-butanediol at a molar ratio of 1/2/1, respectively. At ambient temperature, the tensile properties of the blends typically are intermediate between the values of the two separate components. Characterizations of the dynamic mechanical properties of the blends show the relative degree of compatibility for the thermoplastic urethane elastomer and the respective polymers. Two separate glass transitions are obtained for blends of polystyrene and the styrene-acrylonitrile copolymer with the thermoplastic urethane elastomer. This behavior demonstrates that these blend systems are incompatible. The blends of Phenoxy A and the thermoplastic urethane elastomer exhibit a single glass transition for which the temperature is dependent on the respective concentration of the components. These mixtures are considered to be compatible in nature.

Notes: A new type of extrusion rheometer has been designed which employs dual slit geometry with a double valve. The double valve concept allows a change in flow rates through the slits, while the total extruder flow rate remains constant thus leaving extruder operating conditions unchanged. Electronic pressure transducers are mounted along the slit to record axial pressure distribution. Flow rates are measured by weighing polymer output and wall shear stresses are calculated from the axial pressure profiles. Exit pressures are derived from extrapolating the pressure profile to the slit exit and from this information the normal stresses can be determined.

Notes: Trifunctional poly-ε-caprolactone polyol was polymerized with a chain-extended 1,6-hexane diisocyanate, and the rheology followed by cone and plate flow. Viscosity was found to be independent of shear rate up to at least 102 N.s/m2 (103 poise) and 30s-1. Extent of reaction was monitored by a periodic titration for isocyanate groups. Using branching theory, viscosity was related to extent of reaction and temperature. Such relations should be useful for process models. Normal force data for the curing system are also reported.

Notes: Melt How data has been determined for a series of fractionated and whole low density polyethylenes which has been characterized in terms of their molecular weights and degree of long-chain branching, (LCB). The resulting data indicate that low LCB influences melt flow both through a reduction in molecular size and an increased level of intermolecular interaction. Die swell measurements on whole polymers indicate an increase in melt elasticity with increase in degree of LCB for samples of similar melt flow (MI). Comparison of GPC data with observed die swell characteristics indicates that die swell is a molecular size dependent property and independent of intermolecular entanglement effects, suggesting that the measurement of elastic properties of LDPE melts will provide a means of determining relative degrees of LCB for commercial resins.

Notes: The results of wide angle X-ray diffraction and, ATR polarization measurements are reported in order to characterize the anisotropy in poly(m-phenyleneisophthalamide) and poly(p-phenyleneterephthalamide) (Fiber B) fibers. Additional information on the state of order of the investigated fibers is derived from ATR spectroscopic accessibility measurements by deuterium exchange.

Notes: The theory of deep drawing, which has been developed for metals, is examined critically for thermoplastics. Two special characteristics of thermoplastics, the strong orientation hardening after initial yielding and the ease of crack formation and growth, are shown to vitiate the usual correlation between the drawability of the sheet and the low strain plastic behavior of the material. Attempts to improve the limiting draw ratio of thermoplastics, by biaxially rolling sheet prior to forming, are shown to be effective only if the polymer does not craze easily under tensile stresses.

Notes: This new coupling agent shows promise for use in reinforcing hydrocarbon type polymers, such as polyolefins and polystyrene, with glass fibers and inexpensive mineral fillers. Sulfonyl azide derivatives readily form durable bonds to many thermoplastics at normal extrusion and molding temperatures, without the use of peroxide or sulfur-type curing agents. Alkoxy silanes, attached to the sulfonyl azide, hydrolyze in the known manner forming bonds to inorganic fillers. Using commercial compounding and injection molding procedures, 40 wt percent of mineral fillers containing 1 percentofan azidosilane coupling agent were incorporated in polypropylene. Very substantial improvements in tensile, flexural and heat distortion properties were obtained with little loss in impact strength. An initial evaluation in a filled polystyrene showed significant, but less dramatic, improvements.

Notes: Processing of polymers is greatly affected by the presence of dissolved gases. Analysis of the effect of dissolved gases requires two types of information: equilibrium thermodynamic data and predictive correlations as well as diffusion rate data and analyses. We review here the state-of-the-art knowledge of the equilibrium thermodynamics of gases dissolved in polymers. The published data are presented and analyzed. Also, we review the latcst theories and predictive correlations for gas solubility in polymers.

Notes: A significant advance in ion exchange resin and adsorbent technology has been the development of the macroreticular pore structure. Synthetic rotes have been developed for preparing both ion exchange resins and polymeric adsorbents of high surface area and pore volume. Syntheses have been developed to the degree that the surface area and pore.parameters can be widely varied. Several of these macroreticular polymers based upon the crosslinked styrene and acrylate systems are now available commercially. These polymeric adsorbents are hard, durable, insoluble spheres of high surface area and porosity. They are available in a variety of polarities. The nonpolar adsorbents are particularly effective for adsorbing nonpolar solutes from polar solvents. Conversely, the polar adsorbents are very effective for adsorbing polar solutes from nonpolar solvents. Of particular interest is the use of these polymeric adsorbents for the treatment of effluent wastes. In some cases it has been demonstrated that one can recover significant quantities of re-usable chemicals that more than pay for the waste, treatment. The use of the polymeric adsorbents for the treatment of phenolicwastes is an example. Other related applications include the removal of chlorinated pesticides, TNT residues, and other noxious compounds from waste effluents and water supplies.

Notes: Prior studies of two series of segmented polyurethanes based on 2, 4 toluene cliisocyanate (2, 4 TDI) or 2, 8 TDI, butanediol, and a 1000 molecular weight polytetramethyleneoxide (PTMO-1000) soft segment revealed a rapid increase in soft segment glass transition temperature (Tg) with increasing urethane content in the 2, 4 TDI series. The change in Tg couldbe correlated with estimates of hard segment-soft segment phase mixing obtained by infrared analysis of the urethane NH and carbonyl bands. In the present paper, the infrared data have been reevaluated using improved procedures for resolving the carbonyl band into H-bonded and nonbonded components, and the relation between the estimated extent of phase mixing and Tg has been reexamined. The transition behavior in an extensive series of related polymers has also been determined, including 2, 4 TDI arid 2, 6 TDI samples with PTMO2000 as well as polybutyleneadipate (PBA-1000 and PBA-2000) soft segments. The results indicate the effectiveness, of increased soft segment molecular weight in promoting phase segregation, imply that much greater phase mixing occurs in polyester than polyether samples, suggest that anchoring the ends of the soft segments has only a small effect on Tg, and provide some evidence that H-bonding not only increases Tg but can also impede soft segment crystallization.

Notes: During the injection molding process, moldings undergo shear and elongational stresses. They are also exposed to thermal gradients of varying intensity. Invariably, molded parts, or at least some sections thereof, freeze before the polymer chains can relax to a random, non-oriented configuration. As a result, injection molded parts contain frozen strains and exhibit anisotropic physical properties. In the present work, a variety of experimental techniques have been employed to determine the three-dimensional variation of the following properties of injection-molded, thermoplastic, rectangular parts: density, heat shrinkage, birefringence, and tensile strength.

Notes: Chemorheological changes in epoxy resins subjected to large strains while heated were observed earlier, but the subject was not treated quantitatively. This paper describes the investigation of an epoxy resin - Epon 826, of known chemical, structure, crosslinked with two different amines. By means of a simple calibrated apparatus, the epoxide samples were subjected to large strains in a non-oxidizing atmosphere and in air. They were heated to different temperatures for various times; the results were compared with data obtained from unstrained samples kept in otherwise the same conditions. The results show a linear-logarithmic relation between the torsion modulus, G(10) and the time of applied strain at a certain temperature and also a linear relation between G(10), and 1/T°K, both above T(10). The results obtained in swelling experiments support the data from 10 sec torsional modulus vs temperature measurements. An increase in the amount of solubles and in Mc is observed on extending the time of heating. A clear difference in properties between the strained and unstrained samples, kept in otherwise the sane conditions, is observed and the contribution of the applied strain to chemorheology has been shown. Both systems of crosslinked Epon 826 showed the same general behavior, although the specific data were different.

Notes: The rate of vapor-development of poly(olefin sulfones) subjected to electron beam irradiation is markedly, dependent upon the olefin structure. At room temperature, poly(butene-1sulfone) and poly(cyclopentene sulfone) vapor-develop at rates several orders of magnitude lower than, for example, poly(2-methyl pentene-1 sulfone). Differences in vapor development rate for the various sulfones are shown to be related to differing rates of depolymerization which, in turn, are related to differences in ceiling temperatures for polymer formation. Kinetic analysis indicates that the mechanism involves random scission followed by depropagation and bimolecular termination.