Modeling of Deformation Processes in Vacuum Thermoforming of a Pre-stretched Sheet

Modeling of deformation processes in vacuum thermoforming for a preliminary stretched thermoplastic sheet (plug-assist vacuum thermoforming) is investigated in this paper. The model can be used for production of polymeric articles with minor wall-thickness variation. A nonlinear rheological model is implemented for developing the process model. It describes deformation process of a prestretched sheet at any phase of vacuum thermoforming process. This process is described by a set of deformation processes, each specified by appropriate boundary conditions. For model validation, a comparative analysis of the theoretical and experimental data is presented. The wall-thickness distributions obtained from modeling results corresponded well with experiments. A method for prediction and enhancement of the quality of the final products on the basis of wall-thickness distribution criterion has been established.     

Rheological modeling of fracture in plug‐assisted vacuum thermoforming

The fracture of polymeric sheets is one of the practical problems occurring during plug‐assisted vacuum thermoforming. This defect can occur during both the plug‐assist and vacuum‐forming stages. This article focuses on two issues: (1) the origins of fracture creation and (2) the determination of the process parameters needed for removal of the defect. The results of our work not only lead to an understanding of the cause of this problem but also enable us to calculate the parameters that affect the fracture of polymeric sheets during plug‐assisted vacuum thermoforming. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Wall thickness distribution in plug-assist vacuum formed strawberry containers

An experimental study on the influence of processing parameters namely film temperature, plug velocity, and temperature on wall thickness distribution in plug-assist vacuum thermoformed fresh strawberry container using high-impact polystyrene is presented. Film temperatures of 118, 125, 136, 150, and 165°C, plug velocities of 0.15, 0.20, and 0.27 m/s, and plug temperatures of 25, 60, 100, 123, and 135°C were used in the thermoforming. Increasing the plug velocity resulted in improved wall thickness distribution due to elastic deformation of the plastic sheet during thermoforming. Decreasing the stretching time and the temperature difference between the plastic film and plug was important for good wall thickness distribution. Better wall thickness was obtained at the plug velocity of 0.27 m/s and the plug temperature of 123°C.     

Derivation of optimal processing parameters of polypropylene foam thermoforming by an artificial neural network

The effects of processing parameters on the thermoforming of polymeric foam sheets are highly nonlinear and fully coupled. The complex interconnection of these dominant processing parameters makes the process design a difficult task. In this study, the optimal processing parameters of polypropylene foam thermoforming are obtained by the use of an artificial neural network. Data from tests carried out on a lab‐scale thermoforming machine were used to train an artificial neural network, which serves as an inverse model of the process. The inverse model has the desired product dimensions as inputs and the corresponding processing parameters as outputs. The structure, together with the training methods, of the artificial neural network is also investigated. The feasibility of the proposed method is demonstrated by experimental manufacturing of cups with optimal geometry derived from the finite element method. Except the dimension deviation at one location, which amounts to 17.14%, deviations of the other locations are all below 3.5%. POLYM. ENG. SCI., 45:375–384, 2005. © 2005 Society of Plastics Engineers     

Investigation into thermoformability of hot compacted polypropylene sheet

Abstract

This paper describes an investigation into the thermoformability of a new class of oriented polymeric material recently developed, namely hot compacted polypropylene sheet. Exploitation of any new material requires an intimate understanding of a whole range of factors, amongst which thermoformability is pre-eminent. This is particularly true for oriented polymeric materials, for while the preferred molecular alignment gives enhanced properties such as stiffness, strength, and resistance to impact, the downside is that the stretched molecular chains tend to limit further flow under stress, making thermoforming difficult. The aim of the present study was to establish the critical parameters for successful thermoforming of hot compacted polypropylene sheet.

Elevated temperature tensile tests were used to investigate the stress–strain behaviour of the compacted materials. The crucial parameters were found to be the post-yield modulus, which gives a measure of the resistance of the material to large scale deformation, and the strain to failure, which gives the upper limit on deformation. The post-yield modulus was found to be significantly affected by the test temperature and the high strain hardening behaviour of the material confirmed that significant force is required to thermoform the compacted polypropylene sheets. A hemispherical mould, with built-in gripping plate, was used to carry out a study of the thermoforming behaviour of the compacted sheets, and the results were found broadly to confirm the conclusions of the tensile tests. A linear relationship was found between the tensile force and the postforming force, reinforcing the synergy between the two tests. In addition the forming tests showed that the best temperatures to use were either side of the melting point of the melted and recrystallised phase, depending on the amount of postforming deformation required. Different gripping arrangements were investigated both in which the sheet was fully gripped and in which the sheet was allowed to flow into the mould during forming. The different schemes were found to control whether a successful component could be produced under different conditions and at different ultimate strains. Finally, the tests with the hemispherical mould showed that thermoforming this shape requires significant interlaminar shear deformation, and above 15% strain this resulted in destruction of the interlayer bond. For strains greater than this, successful thermoforming could only be achieved by allowing the material to flow into the mould.     

Thermoforming of liquid crystalline polymer sheets

Liquid crystalline polymer (LCP) extruded sheets were further processed by the conventional thermoforming method. The available processing temperature range was defined through the structural, thermal, and elevated temperature mechanical characterization of the extruded sheet. This temperature range was found for LCP to be quite narrow, in the proximity of the crystal-mesophase transition. The structural changes imposed on the LCP sheet during forming and its thermal stability were investigated using wide angle X-ray diffraction, mainly for the determination of the chain orientation distribution, DSC, and dynamic mechanical analysis. Thermoforming onto a symmetrical male mold was found to enhance the orientation in the extrusion machine direction and even change the preferred orientation in the extrusion transverse direction to orientation along the thermoforming direction. Annealing at the thermoforming temperature range results in a more ordered and thermally stable structure accompanied by just a slight orientation loss.     

Rheological modeling of plug‐assist thermoforming

Solving problems for thermoforming processes in the production of axisymmetric thin walled plastics is investigated in this research work. A nonlinear viscoelastic rheological model with a new strain energy function is suggested for improvement of physical properties of final product. For model validation, a quantitative relation between stress and technical parameters of plug‐assist thermoforming is determined by comparison of theoretical and experimental results. This process with the proposed rheological model could be suggested for prevention from some technical defects such as wall thickness variations, physical instability during inflation‐shrinkage, and warpage exhibited in the final part of a polymeric sheet thermoforming. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4148–4152, 2006     

Uni- and biaxial stretching of chlorinated pvc sheets. A fundamental study of thermoformability

Chlorinated PVC is superior to unmodified PVC as a thermoplastic for use in thermoforming, especially if improved heat resistance and dimensional stability are required. In the present report, results tire given of a fundamental experimental study on the thermoformability of CPVC sheets obtained by calendering various formulations based on CPVC resins with at least 65 percent chlorine content. Extensibility as well as the relationship between stress and strain in uni- and biaxial stretching have been determined as a function of temperature and rate of stretching by means of specially devised, highly instrumented laboratory equipment. Stress-strain relations under isothermal conditions and at constant strain rate are compared for the two modes of stretching, and the difference in behavior between PVC and CPVC, particularly with regard to the effect of temperature, is emphasized. Internal stresses frozen in during cooling, following rapid stretching at appropriate thermoforming temperatures, have been determined by means of a detailed analysis of retractive force measurements. The relationship between internal stress and molecular orientation is discussed as well as the effect of the latter parameters on various properties of technological interest: dimensional stability, impact resistance, and gas permeability.     

Uniaxial tensile behavior and thermoforming characteristics of high barrier EVOH‐based blends of interest in food packaging

The uniaxial tensile characteristics of blends of an ethylene‐vinyl alcohol copolymer (EVOH‐32 mol% ethylene) with an amorphous PA and/or a nylon‐containing ionomer, used as barrier layer in multilayer food packaging structures, was assessed in this paper. The stress‐strain behavior of these materials at elevated temperatures and at different strain rates was examined. The stress‐strain curves obtained were used to understand the influence of temperature and strain rate on the uniaxial deformation process of the materials, these being of general importance during typical processing steps including thermoforming. A male mold for deep‐draw was used to assess the thermoforming (biaxial deformation in nature) behavior of extruded sheets at 100, 120, 140 and 150°C, and the results were broadly found to be in agreement with results from simple uniaxial tensile tests. From the preliminary thermoforming results, it was found that EVOH/aPA extruded blends did not improve the poor formability of EVOH alone. In contrast, significant improvement in thermoformability was achieved by blending EVOH with a compatibilized ionomer. Optimum forming capacity was achieved in a ternary blend by addition of a compatibilized ionomer to an EVOH/aPA blend in the range of 140°C–150°C. The ternary blend showed a lower reduction of thickness in the sidewalls, as well as a higher dimensional uniformity in the thermoformed part. Polym. Eng. Sci. 44:598–608, 2004. © 2004 Society of Plastics Engineers.     

Improved mathematical modeling for the sheet reheat phase during thermoforming

In any thermoforming process, plastic sheet heating is the most important phase as it is responsible for final part quality as well as overall process efficiency and productivity. The goal of the study reported here was to improve existing mathematical models to accurately predict the temperature profile inside a heated sheet, where the model could be used to better control the overall thermoforming process. A mathematical model with temperature dependent, variable sheet material properties including density, thermal diffusivity, specific heat, and thermal conductivity was developed and validated against experimental data. Models with constant and variable plastic sheet properties were created, simulated, and compared in Matlab. The models were validated by experiments which obtained temperature profiles at different depths within a plastic sheet by inserting thermocouples and recording temperatures. Further, the effect of sheet color on heating was investigated by considering two extreme cases: white (transparent) and black (opaque) colored sheets, and the effect of oven air temperature and velocity on sheet heating was also investigated. Results indicated that a variable properties model was needed to control sheet reheating especially with narrow forming windows, and that the heating profiles required for colored and noncolored sheets were very different. POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers     

Advance on processing of compostable and thermally stable biodegradable polyester blends

Flexible and semiflexible packagings can be manufactured by cast extrusion of plastic sheet and thermoforming of containers. Thermal stability is often required as packaging items after being thermoformed can come in contact with hot food/beverage, especially during hot filling operations. In this framework, the present study deals with the design and manufacturing by thermoforming of plastic containers that are, at the same time, compostable and suitable for high-temperature applications (~100 °C). First, extrusion compounding of Poly(l -lactic acid) (PLLA)-based biodegradable polyester blends was performed. In particular, the effect on the material properties of different types of nucleating agents was investigated. Combinations of micro-lamellar talc, poly(d -lactic acid) (PDLA), ethylene bisstearamide (EBS), and titanium dioxide (TiO₂) were studied. The formulations involving EBS boast the highest crystallinity and the fastest onset of the crystalline phase on sheets produced by cast extrusion. Conversely, the formulations involving TiO₂ feature the lowest degree of crystallinity and the slowest onset of the crystalline phase. Combinations of talc and PDLA exhibit an intermediate behavior. Second, thermoforming of the plastic foils was performed. A very different trend of the crystallization after thermoforming is shown. Indeed, crystallinity is the highest for the formulations involving talc and PDLA, the lowest for the ones containing EBS. In conclusion, the biodegradable polyester blends are found to be suitable for the manufacturing of compostable and thermostable packaging items by cast extrusion and thermoforming. Final crystallization of the material and the resulting thermal stability can be fine-tuned by modulating type and amount of nucleating agents. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48722.     

Dynamic characteristics of plug‐assist thermoforming process

Plug‐assist thermoforming is a well‐known technique in polymer processing because of its interesting features. The dynamic value of driving‐force for the stretching process is determined based on equilibrium equation. This amount of force is required for applying to a plug to stretch a sheet. It is used for calculation of the required theoretical work and power of a plug‐assist thermoforming process. By using a nonlinear viscoelastic rheological model in the proposed mathematical model, its validity was examined by performing experimental tests on ABS sheets. POLYM. ENG. SCI., 2009. © 2008 Society of Plastics Engineers     

A Robust Experimental Methodology for Polymer Bubble Inflation

In thermoforming technique thermoplastic sheets are heated up well above their glass transition temperature and formed to the required shape by using an appropriate mold. Characterization of thermoplastic materials for thermoforming can be accomplished by employing polymer bubble inflation and rheology tests instead of undertaking expensive biaxial tensile testing. Polymer bubble inflation technique is very sensitive to process condition variations, so a robust experimental methodology is essential. Design and development of one such experimental system was undertaken by carrying out a variety of preliminary tests. This paper presents the experimental methodology developed for polymer bubble inflation. The developed experimental system demonstrates highly repeatable polymer bubble inflations. Bubble inflations were conducted at different temperatures and different diameter circular clamping using acrylonitrile butadiene styrene (ABS) thermoplastic. Polymer sheet initial sag due to heating and its influence on bubble inflation have been captured by using the experimental system.     

Oxidation of alcohols mediated by a polymer supported potassium ferrate as an effective mild oxidant

The use of polymeric oxidizing agents simplifies routine oxidation of reactions because it eliminates the traditional purification. In this article, the use of the cross‐linked poly (4‐vinylpyridine)‐supported potassium ferrate as an effective mild polymeric oxidizing agent is described. This reagent is capable of oxidizing organic compounds and can be used as a versatile reagent in organic synthesis. Primary and secondary benzylic and allylic alcohols are converted selectively to their carbonyl compounds, and hydroquinone to the 1, 4‐benzoquinone. This polymeric reagent seems to be nontoxic and nonpollutant. Based on our observation during the study, the polymeric reagent is stable and can be stored for months without losing its activity. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Investigation of polymerization parameters affecting dopamine selectivity of a polymeric membrane

Summary By means of electrochemical oxidative polymerization, poly (1,3-phenylenediamine) films on a gold electrode were prepared at a potential of 0.8 V. The permeation properties of polymeric films at the different thickness were investigated by cyclic and differential pulse voltammetry techniques. Voltammetric studies showed that polymeric film at the 1.2 mC thickness exhibited selective permeation for dopamine while rejecting ascorbic acid. Then, all the polymerization parameters affecting the permselective characteristics were systematically investigated and the optimal values were determined. Moreover, stability of polymeric membrane was examined. The results showed that polymeric membrane, owing to permselective character, could be used as a dopamine selective membrane. Received: 10 December 1999/Revised version: 12 March 2000/Accepted: 27 March 2000     

Electron Paramagnetic Resonance Studies of the Effect of Temperature on Polymeric Radiation Dosimeters

Abstract

Electron Paramagnetic Resonance (EPR) and infrared spectroscopy were employed to study the effect of the temperature at which a polymeric radiation detector operates during electron irradiation process. The results demonstrate that the rate at which the free radicals created in the polymer by the irradiation recombine, changes with the temperature applied during the actual irradiation.     

Development of a multivariable online monitoring system for the thermoforming process

The thermoforming industry has been relatively slow to embrace modern measurement technologies. As a result researchers have struggled to develop accurate thermoforming simulations as some of the key aspects of the process remain poorly understood. For the first time, this work reports the development of a prototype multivariable instrumentation system for use in thermoforming. The system contains sensors for plug force, plug displacement, air pressure and temperature, plug temperature, and sheet temperature. Initially, it was developed to fit the tooling on a laboratory thermoforming machine, but later its performance was validated by installing it on a similar industrial tool. Throughout its development, providing access for the various sensors and their cabling was the most challenging task. In testing, all of the sensors performed well and the data collected has given a powerful insight into the operation of the process. In particular, it has shown that both the air and plug temperatures stabilize at more than 80°C during the continuous thermoforming of amorphous polyethylene terephthalate (aPET) sheet at 110°C. The work also highlighted significant differences in the timing and magnitude of the cavity pressures reached in the two thermoforming machines. The prototype system has considerable potential for further development. POLYM. ENG. SCI., 54:2815–2823, 2014. © 2014 Society of Plastics Engineers     

Production of thin graphite sheets for a high electrical conductivity film by the mechanical delamination of ternary graphite intercalation compounds

Herein we propose a production scheme for conductive films composed of thin graphite sheets with high crystallinity and polymeric resin. The crystalline graphite sheets were successfully produced from natural graphite powder by solution-phase synthesis of graphite intercalation compounds (GICs), following a wet planetary-ball milling under mild conditions. The shear forces in the milling pot lead to a peeling of graphite flakes. Taking into consideration the interlayer bonding force, the delamination should be preferentially done from the expanded GICs interlayer rather than intrinsic graphite one. Some composite films derived from the phenolic resin and flaky graphite sheets displayed much higher electrical conductivities compared to the film from the feed graphite particles. We also demonstrate the stage structure of synthetic GICs affected the film conductivity. The composite films made from exfoliated products of ground (around stage IV) GICs exhibited high electrical conductivity with a small amount of the graphite sheets.     

Synthesis and characterization of polystyrene initiated using polymeric peroxide

Polymer peroxides were synthesized by copolymerizing tert‐butyl‐3‐isopropenylcumylperoxide (D‐120) with styrene (St). Exothermic peak at 192.7°C in DSC thermogram indicated that peroxy bonds in D‐120 remained intact during the copolymerizing process. The polymeric peroxide was used to initiate polymerization of St. GPC results showed that polystyrene (PS) initiated by the polymeric peroxides was composed of both linear and branched molecules. In addition, the rheology test showed that PS samples initiated by polymeric peroxide contained branched structure and had lower shear viscosities. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 197–202, 2006