The SPE Library contains thousands of papers, presentations, journal briefs and recorded webinars from the best minds in the Plastics Industry. Spanning almost two decades, this collection of published research and development work in polymer science and plastics technology is a wealth of knowledge and information for anyone involved in plastics.
To investigate the possible formation of polymer/clay nanocomposites halogenated polymers were melt compounded with montmorillonite clays. Natural and organic-treated montmorillonite clays were melt compounded with chlorinated and fluorinated polymers. The formation of polymer nanocomposites was confirmed by X-ray diffraction (WAXS) and transmission electron microscopy (TEM) characterizations. All chlorinated polymers studied including polyvinyl chloride (PVC), chlorinated polyethylene (CPE), polychloroprene (CR), polyvinylidene chloride (PVDC), chlorinated PVC (CPVC), and VDF containing fluoropolymers, polyvinylidene fluoride (PVDF), poly(vinylidene fluoride – hexafluoropropylene) P(VDF-HFP), poly(vinylidene fluoride – hexafluoropropylene – tetrafluoroethylene) P(VDF-HFP-TFE), poly(vinylidene fluoride – tetrafluoroethylene – perfluoromethyl vinyl ether – curesitemonomer) P(VDF-TFE-MVE-CSM) produced polymer/clay nanocomposites with organic-treated montmorillonite clay. Either polyolefin or natural montmorillonite clay did not form nanocomposites. The organophilicity of organoclays and polarity of halogenated polymers seems to contribute to the creation of polymer nanocomposites. The polarity of polymers could be estimated by Debye equation which shows the relationship between dipole moment and dielectric constant. The dielectric constant of polymers could be conveniently used to predict the successful formation of polymer/clay nanocomposites by melt intercalation.
Solution rheological analyses of polyampholyte terpolymers composed of acrylamide (AM), sodium 3- acrylamido-3-methylbutanoate (NaAMB), 3- acrylamidopropyltrimethylammonium chloride (APTAC) were performed at varying polymer concentrations, solution pHs, NaCl concentrations, and molecular weights (MW). Steady-state shear sweeps and dynamic frequency sweeps of semi-dilute solutions were used to measure solution viscosity and viscoelasticity. Results are interpreted in terms of how experimental variables affect the solutions’ electrostatic charges and polymer/solvent interactions, which ultimately affect rheological properties.
Our recent studies have shown that high levels of montmorillonite clay can be added to nylon 12 elastomers to achieve UL-94 rating in 1/8” thickness with minor detrimental effects on physical properties.In the past, in order to achieve this rating we had to use levels of flame retardant systems containing halogen and antimony oxide in excess of fifty percent by weight. This high level of flame retardant had detrimental effects on both the physical properties and the environment.Our goal was to reduce the use of this type of flame retardant system by twenty five percent and still maintain good physical properties. In fact our previous studies show that both impact and flexural modulus increase with increasing levels of nano clay with minimal reduction of elongation.
The major objective of this research was to modify poly(lactic acid) (PLA) film surfaces with an ultimate aim of making a bioactive surface that will show selective protein adsorption and faster degradation. The PLA film was solvent cast and the film surfaces were activated by a plasma treatment procedure or UV irradiation. Poly(acrylic acid) (PAA) was then grafted to the PLA film surface using a UV induced photopolymerization process. The film surface resulting from each reaction step was analyzed using ATR-FTIR spectroscopy and contact angle measurements. The molecular weight of the grafted PAA film was estimated by measuring the molecular weight of the homopolymer formed in the solution during the reaction using GPC. Results showed that PAA (Mw ~ 2000) was grafted from PLA film surfaces in 2 or 3 h depending on the method of activation.
The solid phase graft copolymerization method was used to graft maleic anhydride onto commercial polyethylenes. This process is environmentally friendly since it requires minimal recovery or no use of solvent and the process conditions are mild. NMR analysis confirms the successful grafting of maleic anhydride onto the backbones of both linear low-density polyethylene (LLDPE) and ultra high molecular weight polyethylene (UHMWPE). Graft levels for all the polymers were quantified by FTIR absorbance as well as wet-chemical titration. Significant processing parameters were identified based on statistical design of experiments.
Consideration is given to ongoing developments in the fire performance of formulation variants of EVA copolymer containing zinc hydroxystannate (ZHS), alumina trihydrate (ATH), magnesium hydroxide (MH) and nanoclay mixtures. ZHS/MH combinations are shown to give the best performance in EVA, enabling significant reductions in overall filler levels to achieve an acceptable level of fire performance, however this is dependent on the grade of MH used. The fire resistance of these systems is further improved by small additions of silicate layer nanoclay. The ZHS is shown to function predominantly in the condensed (char) phase.
Cement-based materials are widely used in the civil infrastructure. Polymers as admixtures can improve the properties, particularly in relation to water absorption reduction, toughness enhancement, vibration damping and increase of the bond strength of cement to reinforcements. Polymeric admixtures include particles, short fibers and organic liquids. Latex in the form of an aqueous particle dispersion is most common. Other than being used as admixtures, polymers are used as partial replacement of fine aggregate, for coating, sealing and repairing concrete and for coating steel reinforcing bars for corrosion protection.
This work is part of a study aimed at creating tunable surface modifying layers. Polymer molecules were grafted at the polymer surface and the pendant groups of these grafted polymers were subsequently substituted. The polymer layer of interest in this study was poly(tert-butyl acrylate) (PtBuA) because it is relatively easy to substitute the tert-butyl ester groups with other functional groups to create a chemically tailored layer. The PtBuA was grown from the surface of ethylene-acrylic acid copolymer via atom transfer radical polymerization and was also grafted to the surface using end-functionalized PtBuA. The progression of the reactions and properties of the modified surfaces were studied using ATR-FTIR spectroscopy and static contact angle.
A design is not finished until parts hit the store shelf. There are a number of steps between the first sketches on a napkin and commercial sales, any one of which could lead to delays and cost overruns. One of the most important design considerations is material selection. Plastic parts are unique in that the material is infinitely variable. Designers working off of raw material specifications can set themselves up for some counterproductive surprises. Colorants, flame retardants, mold releases, ultraviolet light stabilizers and regrind affect melt viscosity and physical properties. By looking at final resin formulations early in the design process, manufacturing and performance issues can be addressed when changes are least costly. ColorWorks is an integrated solutions tool to help designers get to the final material properties quickly.
Finite Element Method (FEM) calculations are suitable for predicting the mechanical behavior of plastic products with complex geometries. The problem is to obtain to the relevant material data in particular for thin walled sections. Results from laboratory tensile specimens are not very reliable, because they are relatively thick and have little orientation.To determine the influence of thickness and orientation, creep and recovery experiments have been carried out. The specimens had different thicknesses and different flow directions. The results from tests have been used for FEM-calculations to determine the influence of thickness and orientation on the mechanical behavior of a beam shaped product.
Many industries, such as the automotive industry, are faced with a high volume of plastics scrap associated with painted plastic parts. Ideally, the paint is removed prior to reuse of the painted regrind. Paint removal methods include differential thermal expansion, chemical attack and abrasion. If not removed, paint flakes in the regrind material influence the mechanical properties and aesthetics of the product molded from the painted regrind. The size of the paint flakes will likely have an influence on the mechanical properties of the molded part.A reground painted thermoplastic olefin (TPO) will be extruded using a general purpose and a “grater” screw being developed at UML. The grater section design will then be modified to implement a progressive grating technique. The effect of the design change on paint flake size, output, melt temperature and mechanical properties will be monitored.
Gate location is an important aspect of thermoplastic part design, and injection mold design. A proper gate location will facilitate high quality parts, whereas poor gate location may cause the quality of the part to suffer. There are many different factors that affect the gate location. These factors that may affect gate location include: flow properties of the plastic, gating into the approximate center of the part, wall thickness, gating into an obstacle, style of the gate, separation of the runner system from the part, aesthetic properties, and ease of manufacturing. Computer simulations may help to facilitate the proper gate location and decrease the lead-time in producing a mold.The focus of this research project is to determine the ideal gate location given the previously mentioned factors for a single gated thermoplastic part, comparing both the experience of previous engineers through research of current materials, and the analysis of computer simulation software. The first portion of this project consists of research compiled from accredited individuals within the plastics industry; their perspectives and experiences have been combined to discuss the various possibilities in placing an ideal gate location. Following the research, these ideas were tested through the use of Mold Flow (Mold Flow Inc.) in various part designs. The last portion of this project compares and contrasts the industry experience to the results of the simulation software.
Formulators are constantly being asked to lower cost, improve performance, or both. This paper addresses this problem by reporting on the evaluation of an old standard calcium stearate paraffin lube system and one micron filler, vs. sub-micron fillers with ester modified lube systems.In the past this approach has been successful in allowing the use of lower modifier levels, or higher filler levels, without loss of properties, with modifier levels lowered from 4.5 to 3.0phr. This paper answers the question, “Is there any merit to using this approach when the modifier ranges from 2 to 0phr?” with the goal of eliminating the modifier altogether.
In this study, a novel reactive blending technique was used to produce poly (vinyl chloride) (PVC)/thermoplastic polyurethane (TPU) blends that are otherwise difficult to produce by a conventional melt blending techniques due to degradation at elevated processing temperatures. Morphological and spectral characterization studies revealed that reactive blending process generated better mixing relative to melt blending process. The miscibility of the PVC with the polyols of the TPU and with the TPU was studied by changing in the chemical structure of the polyol.
Major factors affecting short term and longterm performance of plastics in engineering applications include a) chemical makeup and molecular architecture, additives etc; b) material and parts manufacturing conditions; c) installation and service conditions that include load, loading rate, temperature and other environmental conditions. Successful design of plastic components for intended application requires an understanding of the role of the above factors together with economic considerations that account for a cost of fabrication as well as for a price of failure. Material characterization and ranking with respect to strength, toughness and durability provide a basis for rational design with plastics. There are industrial standards and regulations develop to assist in product selection. Advantages and limitations of widely publicized standards and methods for durability and lifetime of engineering thermoplastics will be illustrated by examples of field failure analysis. Methodology of material durability and structural reliability assessment will be discussed.
The physical and mechanical behavior of nano-scale reinforced polymers is currently receiving a significant amount of interest in the scientific arena. One of the more controversial aspects discussed is associated with the role the interface has on the physical state and bulk properties of the resulting composite. Another aspect is that associated with length scale effects necessary for energy dissipation in polymer matrix composites and the role of nanocomposites in this arena. These issues are discussed in contrast to reinforcements evaluated over a range of length scales ranging between micron and molecular length scases.
The traditional method to compare different types and grades of plastics as to their performance potential for pressurised plastics pipes consists of stress rupture experiments with pipes under constant internal pressure. Based upon the observation that long-term pipe failure generally is governed by a two stage process consisting of a crack initiation stage and a period of stable, slow crack growth (SCG), various methods of fracture mechanics have been applied in the last two decades to study and characterise the SCG resistance of PE pipe grade materials.The paper will provide an overview of the various approaches including concepts of linear elastic fracture mechanics (LEFM) and elastic-plastic fracture mechanics (EPFM), with a particular focus on their applicability and limitations in terms of lifetime prediction, on the one hand, and their potential for quick material comparisons and material rankings, on the other. From an experimental point of view the characterisation methods include monotonic fracture tests over a wide loading rate range, creep crack growth and fatigue crack growth tests, and full notch creep tests (FNCT) with square and round bar specimens in air and liquid surfactant environments.
Tear resistance is a critical requirement for polymeric film for applications such as packaging and imaging. Tear resistance is measured using the Elmendorf tear, trouser tear, and single edge notch tests. It was observed that in many cases the increase of tear resistance was results of crack curving. The mechanism of crack curving and the effect of process zone on crack curving are investigated in this paper. Crack curving during tear process is attributed to the process zone geometry, material orientation or damage orientation inside the process zone, and the large stretching or crack bluntness that create a mix mode fracture process. The effect of film orientation on process zone formation, crack curving, and the tear resistance is also investigated.
The Stress Corrosion Cracking (also called Environmental Stress Cracking) process in Polybutylene (PB) tubing consists of three stages: 1) Crack initiation, 2) Slow crack growth, and 3) Dynamic crack propagation. The first two stages primarily determine the useful lifetime of PB tubing, since the third stage occurs in a relatively short time interval. In this paper, an examination of PB field failures, observation of crack initiation mechanisms, and evidences of chemical degradation as a primary cause of failure are presented. To evaluate crack initiation time in mechno-chemical conditions, a modification of ASTM standard environmental stress cracking technique is employed to accelerate the crack initiation process in PB and a simple extrapolation technique is proposed to estimate the time of crack initiation in service conditions.
Polyphthalamide (PPA) with fiber reinforcement is widely used in electronics as connector housing materials. In high temperature applications, the material undergoes creep. Creep deformation is further amplified when the material is under mechanical loading. This paper addresses PPA creep under temperature and compression loading. A modified time hardening model is shown to fit the experimental data very well. All parameters for the modified time hardening model are provided in the paper. Creep strain as a function of temperature, stress and time is discussed in details. Finite element model is presented to analyze creep strain for application conditions. For a screw tightening mechanism where PPA is under compression, clamping retention is analyzed as a result of material creep. Final discussions also include interactions between creep and pressure relaxation caused by creep, and its effect on clamping retention.
Any article that is cited in another manuscript or other work is required to use the correct reference style. Below is an example of the reference style for SPE articles:
Brown, H. L. and Jones, D. H. 2016, May.
"Insert title of paper here in quotes,"
ANTEC 2016 - Indianapolis, Indiana, USA May 23-25, 2016. [On-line].
Society of Plastics Engineers
Note: if there are more than three authors you may use the first author's name and et al. EG Brown, H. L. et al.
If you need help with citations, visit www.citationmachine.net