Preparation and characterization of high‐performance poly(ether ether ketone) fibers with improved spinnability based on thermotropic liquid crystalline poly(aryl ether ketone) copolymer

High‐performance poly(ether ether ketone) (PEEK) fibers were prepared by melt‐spinning in the presence of thermotropic liquid crystalline poly(aryl ether ketone) copolymer (FPAEKLCP). The rheological and mechanical properties, birefringence, orientation, and crystallization of the resulting PEEK/FPAEKLCP fibers were characterized by using a melt flow indexer, capillary rheometer, single fiber electronic tensile strength tester, polarized light microscopy (PLM), and wide‐angle X‐ray diffraction (WAXD), respectively. The results indicate that the melt viscosity of PEEK significantly reduced by introducing FPAEKLCP, followed by the improvements in the spinnability and the quality of as‐spun fibers. The tensile properties of PEEK/FPAEKLCP fibers mainly depend on the content of FPAEKLCP, drawing temperature, drawing ratio, and annealing processes. Moreover, the tensile strength and modulus of PEEK/FPAEKLCP fibers are obviously higher than those of neat PEEK fibers under the same processing conditions. This should be attributed to an enhancement in the orientation and crystallization of PEEK compounded with FPAEKLCP. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1406‐1414, 2013     

Enhancing resistance of poly(ether ketone ketone) to high-temperature steam through crosslinking and crystallization control

Poly(aryl ether ketone)s (PAEKs) are promising materials for harsh environments, such as in high-temperature steam applications. Here, the effect of high-temperature steam on the crystallinity and mechanical properties of existing poly(ether ether ketone) (PEEK) and PEKK(T/I) polymers is investigated. Differential scanning calorimetry (DSC), wide-angle X-ray scattering or diffraction (WAXD), and dynamic mechanical analysis experiments show these materials undergo significant crystallization and reorganization after prolonged exposure to steam and suffer from embrittlement. In addition, we show that xanthydrol-based crosslinks can provide the dimensional stability and stabilize the PEKK crystal structure. Mechanical tests demonstrate that the ductility is preserved for longer exposures to steam compared to neat PEKK, whereas DSC and WAXD data indicate xanthydrol crosslinks effectively stabilize the crystal structure against steam-assisted crystallization. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47727.     

Rheological properties in blends of poly(aryl ether ether ketone) and liquid crystalline poly(aryl ether ketone)

Rheological properties of the blends of poly(aryl ether ether ketone) (PEEK) with liquid crystalline poly(aryl ether ketone) containing substituted 3‐trifluoromethylbenzene side group (F‐PAEK), prepared by solution precipitation, have been investigated by rheometer. Dynamic rheological behaviors of the blends under the oscillatory shear mode are strongly dependent on blend composition. For PEEK‐rich blends, the systems show flow curves similar to those of the pure PEEK, i.e., dynamic storage modulus G′ is larger than dynamic loss modulus G″, showing the feature of elastic fluid. For F‐PAEK‐rich systems, the rheological behavior of the blends has a resemblance to pure F‐PAEK, i.e., G″ is greater than G′, showing the characteristic of viscous fluid. When the PEEK content is in the range of 50–70%, the blends exhibit an unusual rheological behavior, which is the result of phase inversion between the two components. Moreover, as a whole, the complex viscosity values of the blends are between those of two pure polymers and decrease with increasing F‐PAEK content. However, at 50% weight fraction of PEEK, the viscosity‐composition curves exhibit a local maximum, which may be mainly attributed to the phase separation of two components at such a composition. The changes of G′ and G″ with composition show a trend similar to that of complex viscosity. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4040–4044, 2006     

Rheology of concentrated sulfonated poly(ether ether ketone) solutions

Sulfonated polyether ether ketone (SPEEK), an ionic polymer, has been shown to be a potential candidate for fuel cell electrolyte as a proton exchange membrane. Rheological behavior of SPEEK solutions is of great interest to understand the molecular associations as well as due to implications in membrane processing. In this work, SPEEK of various degrees of sulfonation (58–80) was prepared and rheology of concentrated solutions of SPEEK was studied. The rheological properties were evaluated using steady and oscillatory shear. It was found that steady shear viscosity and storage modulus at any given concentration, is the highest for the lowest degree of sulfonation SPEEK solutions in N‐methyl‐2‐pyrrolidone. The low frequency plateau in storage modulus was observed at some combinations of degrees of sulfonation and concentrations, indicating gel‐like behavior in these SPEEK solutions. No significant change in rheological behavior was observed with different polar solvents. Increase of several orders of magnitude in viscosity, storage and loss moduli were observed with increasing concentrations. The role of hydrophobic aggregation and inter‐chain associations in determining rheology of SPEEK solutions is argued based on comparisons with other material systems. The rheological behavior of SPEEK solutions with 70 as the degree of sulfonation, suggests crossover from hydrophobic‐hydrophilic balance. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40044.     

Developing critical extrusion parameters for nylon 6, nylon 66, and nylon 46 polyamide from the rheology data

This paper describes a new approach to the rheological characterization of engineering plastics such as nylon 6, 66, and 46 polyamides using a capillary rheometer. The melt viscosity data as a function of temperature, shear rate, and residence time were measured and evaluated to demonstrate how to accurately predict critical extrusion parameters, such as barrel temperature profile, stock temperature window, and the screw design requirements, for extruding strip, tubing, and profiles. The results of this work provide a practical and simple quality control tool to select a polyamide resin for optimum processing, and to develop critical processing parameters for extrusion.     

Studies of molecular weight distribution,particle morphology,and rheological behavior of ultra-high molecular weight suspension PVC

In this paper, the particle characteristics and rheological behavior of ultra-high molecular weight PVC (UHMWPVC) produced in both Japan and mainland China were studied. The molecular weight and its distribution of UHMWPVC were measured by GPC. By means of a series of techniques such as SEM, the measurement of surface pore size, plasticizer absorption, and photographic analysis, the morphology and general characteristics of UHMWPVC particles were investigated. A model of particle structure was proposed. It was found that compared to general PVC, UHMWPVC resins are more porous, having better plasticizer absorption properties. Similarly, compared to UHMWPVC made in mainland China, UHMWPVC made in Japan possesses particle characteristics preferred in PVC processing. In the studies of rheological behavior, the programmed temperature Brabender torque rheometer was used to study and compare the melting process of UHMWPVC resins and their plasticized systems under the same shear stress. The capillary rheometer and Brabender extrusion-rheometer were applied to investigate the rheological and extrusion properties of the plasticized systems mentioned above. The results showed that in melting and extrusion process, the particle characteristics of UHMWPVC result in the easy breakage of particles and the formation of “molecular flow,” On the other hand, the high molecular weight is unfavorable to processing. Generally speaking, much more research work is needed to improve the flow properties of UHMWPVC.     

Effect of boron nitride on melt fracture phenomena and processability of lldpe during extrusion

Melt fractures related to processing instabilities limit processing rates in many commercially important polymer processing operations, such as fiber spinning, film blowing, extrusion, and various coating flows. Therefore, melt fracture is responsible for deteriorating the quality and the mechanical properties of final products for rates greater than a critical processing one at which melt fracture occurs. In this study, a commercial linear low-density polyethylene (LLDPE) was modified by adding a small amount of boron nitride (BN) during extrusion in order to improve processability. Capillary rheometry was used to assess processability at various temperatures, levels of applied shear rate, and the length-to-diameter (L/D) ratio for both the pure resin and resins containing boron nitride. Also, parallel-plate rheometry was used to evaluate the dynamic rheological properties of these resins. The relationship between the characteristic relaxation time and the critical shear rate for the onset of melt fracture and slip is discussed.     

Improving rheological property of polymer melt via low frequency melt vibration

A pulse pressure was superimposed on the melt flow in extrusion, called vibration extrusion. A die (L/D = 17.5) was attached to this device to study the rheological properties of an amorphous polymer (ABS) and semicrystalline polymer (PP, HDPE), prepared in the vibration field, and the conventional extrusion were studied for comparison. Results show that the melt vibration technique is an effective processing tool for improving the polymer melt flow behavior for both crystalline and amorphous polymers. The enhanced melt rheological property is also explained in terms of shear thinning criteria. Increasing with vibration frequency, extruded at constant vibration pressure amplitude, the viscosity decreases sharply, and so does when increasing vibration pressure amplitude at a constant vibrational frequency. The effect of vibrational field on melt rheological behavior depends greatly on the melt temperature, and the great decrease in viscosity is obtained at low temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5292–5296, 2006     

Synthesis and properties of novel poly(phthalazinone ether ketone ketone)

A novel poly(phthalazinone ether ketone ketone) was prepared via the nucleophilic substitution polycondensation of bis-1,4-(4-chlorobenzoyl)benzene and 4-(4-hydroxyphenyl)-2,3-phthalazin-1-one. The synthesized polymer exhibited high glass-transition temperature, excellent thermooxidative properties, and fair rheological properties. The polymer was soluble in some polar solvents. Electronic friction and membrane properties are also discussed. The results indicate that the polymer falls in the class of high temperature resistance engineering plastics. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 823–826, 2001     

Blown film extrusion of poly(lactic acid) without melt strength enhancers

Processing strategies were developed to manufacture poly(lactic acid) (PLA) blown films without melt strength enhancers (MSEs). The effects of processing temperature on PLA's melt properties (shear and elongational viscosities), PLA grades, and other processing conditions [ratio of take‐up roller to extruder's rotational screw speeds or processing speed ratio (PSR) and internal air pressures] on film's blow‐up ratio were examined. Experimental results indicate that extrusion‐blown amorphous and semicrystalline PLA films can be successfully manufactured without MSEs by controlling melt rheology through processing temperature and other extrusion processing conditions. PLA processed at lower extrusion temperature had higher melt viscosities, which favored the formation of stable films depending on the PSR and internal air pressure used. Inappropriate control of PSR and internal air pressure led to unstable films with various processing defects such as melt sag, bubble dancing, or draw resonance, irrespective of the lower extrusion processing temperature. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45212.     

EPDM橡胶的流变特性实验研究

为了研究橡胶熔体流变性能对其加工成型的影响，利用毛细管流变仪对三元乙丙橡胶（EPDM）的流变特性进行了实验研究。实验结果表明：EPDM橡胶在毛细管挤出时，剪切速率对剪切应力、剪切粘度和挤出胀大的影响最大；挤出温度对三者有一定的影响；在长径比相同时，毛细管半径对剪切应力和剪切粘度几乎没有影响，但对挤出胀大影响较大。     

Rheological behavior of ethylene–octene copolymer vulcanizates: Effect of blowing agent and precipitated silica filler

An experimental study of the rheological behavior of ethylene–octene copolymer vulcanizates in extrusion containing blowing agent has been carried out. The cell morphology development has been studied through a scanning electron microscope. Rheological properties of unfilled and precipitated silica‐filled systems with variations of blowing agent, extrusion temperature, and shear rate have been studied by using a Monsanto processibility tester (MPT). The total extrusion pressure (P_T), apparent shear stress (τ_wa), apparent viscosity (η_a), and die swell (%) of the unfilled and silica‐filled compounds have been determined by using MPT. The effect of blowing agent (ADC) on the rheological properties of the vulcanizates has also been investigated. There is a reduction of stress and viscosity with blowing agent loading. It was observed that the incorporation of a blowing agent led to decreased shear thinning behavior resulting in an increase in power law index. The viscosity reduction factor (VRF) of unfilled vulcanizates is found to be dependent on the concentration of the blowing agent, shear rate, and temperature, whereas VRF of silica‐filled vulcanizates is found to be dependent on shear rate, temperature, and blowing agent concentration. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1132–1138, 2003     

Rheological properties of phenophthalein poly(ether ether ketone)

The rheological properties of the novel engineering thermoplastic phenophthalein poly(ether ether ketone) (PEK-C) have been investigated using both a rotational and a capillary rheometer. The dependence of the viscosity on the shear rate and temperature was obtained. The activation energy was evaluated both from the Arrhenius and the Williams-Landel-Ferry (WLF) equation. An estimate for the proper E_η (dependent only on the chemical structure of the polymer) has been found from the WLF equation at temperatures about T_g + 200°C. Measurements of the die swell have been performed. The first normal stress differences were evaluated from the die swell results and compared with the values obtained from the rotational rheometer at low shear rates.     

Rheological behaviour of copoly(ethylene/octene) elastomer compunds: Effect of blowing agent and precipitated CaCO3 filler

Abstract

An experimental study of the rheological behaviour of ethylene/octene copolymer compounds in extrusion containing blowing agent has been carried out. The cell morphology development was studied using scanning electron microscopy. Rheological properties of unfilled and precipitated CaCO₃ filled systems with various blowing agents, extrusion temperatures, and shear rates were studied using a capillary rheometer. The total extrusion pressure, apparent shear stress, apparent viscosity, and die swell of the unfilled and CaCO₃ filled compounds were also determined and the effect of blowing agent on the rheological properties of the compounds studied. It was observed that there is reduction of stress and viscosity with blowing agent loading. Incorporation of blowing agent led to decreased shear thinning behaviour resulting in an increase in the power law index. The viscosity reduction factor of the unfilled compound was found to be dependent on the concentration of blowing agent, the shear rate, and the temperature.     

The effect of extrusion processing conditions on EVOH/clay nanocomposites at low organo‐clay contents

Ethylene vinyl alcohol (EVOH) copolymer is studied as a host for low concentrations, up to 1 wt%, of organically treated clay. The clay develops a high interaction level with EVOH and thus high torque levels accompany the structuring process leading to the formation of nanocomposites. Extrusion residence time, successive extrusion passes, screw rotational speed, and processing temperature were all found to affect the morphology and the thermal and mechanical properties of the resulting composites. The extrusion compounded composites were subsequently injection molded. A subtle balance of processing parameters is required to achieve improved properties. Long extrusion residence times were found important for good clay dispersion in some cases, whereas in other cases an exfoliated structure was obtained already after the first extrusion pass. Two organically treated clay types processed at the same conditions were examined, and found to result in different morphology and mechanical behavior. Compression molding of extrusion compounded materials, under several extrusion conditions, was studied to illustrate the effect of shear level on the resulting morphology. The delamination level was higher after compression molding compared to that after injection molding. EVOH thermal properties and thermal stability of the related composites were also examined using differential scanning calorimetry and thermal gravimetric analysis. Higher extrusion processing temperature (220 compared to 200°C) was found to change the crystallization process of EVOH in the presence of clay, leading to significant decrease in T_m and T_c compared to that of the neat EVOH. POLYM. COMPOS., 26:343–351, 2005. © 2005 Society of Plastics Engineers     

Effect of dynamic cross‐linking on melt rheological properties of polypropylene/ethylene‐propylene‐diene rubber blends

Study of melts rheological properties of unvulcanized and dynamically vulcanized polypropylene (PP)/ethylene‐propylene‐diene rubber (EPDM) blends, at blending ratios 10–40 wt %, EPDM, are reported. Blends were prepared by melt mixing in an internal mixer at 190°C and rheological parameters have been evaluated at 220°C by single screw capillary rheometer. Vulcanization was performed with dimethylol phenolic resin. The effects of (i) blend composition; (ii) shear rate or shear stress on melt viscosity; (iii) shear sensitivity and flow characteristics at processing shear; (iv) melt elasticity of the extrudate; and (v) dynamic cross‐linking effect on the processing characteristics of the blends were studied. The melt viscosity increases with increasing EPDM concentration and decreased with increasing intensity of the shear mixing for all compositions. In comparison to the unvulcanized blends, dynamically vulcanized blends display highly pseudoplastic behavior provides unique processing characteristics that enable to perform well in both injection molding and extusion. The high viscosity at low shear rate provides the integrity of the extrudate during extrusion, and the low viscosity at high shear rate enables low injection pressure and less injection time. The low die‐swell characteristics of vulcanizate blends also give high precision for dimensional control during extrusion. The property differences for vulcanizate blends have also been explained in the light of differences in the morphology developed. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 1488–1505, 2000     

Rheological study of copovidone and solid dispersion blend used for hot melt extrusion

The focus of this work is to generate rheological parameters using AR 2000EX rheometer for PVP VA64 and Compound A – PVP VA64 blend at different temperatures, which can then be subsequently used to identify hot melt extrusion process conditions. Addition of Compound A to the neat PVP VA64 shows a drop in storage modulus and loss modulus as compared to the neat PVP VA64. It appears that Compound A is acting as a plasticizer by increasing the separation of the polymer chains and thus results in reduction of viscosity of Compound A blends compared to polymer only samples. For both systems, based on low standard error of fit, Cross model was chosen as the best fit for the rheological data and temperature dependency of viscosity was assessed by Williams–Landel–Ferry (WLF) model. This approach can be applied to screen formulations with new chemical entities (NCEs) and generate rheological information with various extruding polymers at fixed/variable drug loading in polymer matrix to determine suitability for hot melt extrusion process and appropriate temperature for conducting hot melt extrusion. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43278.     

Rheological behavior of highly filled ethylene propylene diene rubber compounds

The rheological behavior of highly filled ethylene propylene diene rubber (EPDM) compounds was studied with respect to the effect of curative system, grafted rubber, shear rate, temperature and die swell using a Monsanto Processability Tester (MPT) to gain an understanding of the molecular parameters that control the surface finish. All systems show pseudoplastic behavior. At a particular shear rate, shear viscosity increases with blend ratio. The dependence of flow behavior on extrusion velocity indicates a surface effect. The extrudate die swell and maximum recoverable deformation are related by a linear relationship, which is independent of sulfur/accelerator ratio, extrusion temperature and shear rates and blend ratio. The principal normal stress difference increases nonlinearly with shear stress. Activation energy decreases with shear rate in most cases. The faster relaxing system produces extrudate of better surface quality.     

Synthesis of poly(ether ether ketone)-block-polyimide copolymer and its compatibilization for poly(ether ether ketone)/thermoplastic polyimide blends

Novel poly(ether ether ketone)-block-polyimide copolymers (PEEK-b-PI) with different block length were prepared by the polycondensation of amino-terminated poly(ether ether ketone) oligomer and anhydride-terminated polyamic acid oligomer. As the compatibility agent, PEEK-b-PI was added to the poly(ether ether ketone)/thermoplastic polyimide (PEEK/TPI) blend, and blends of PEEK/TPI/PEEK-b-PI were prepared by melt extrusion. Morphology observation showed the domain size of the dispersed phase was significantly reduced with the addition of PEEK-b-PI having optimized block length, which suggested reduced interfacial tension and enhanced interfacial adhesion. The compatibilizing effect was further proven by the change of the glass transition temperature of PEEK and TPI, which shifted closer to each other. As a result, the mechanical properties of PEEK/TPI blends were significantly improved with the addition of the PEEK-b-PI. In particular, 5 wt% content of PEEK-b-PI can increase the elongation at break of the blend by about 200%.     

Effect of powders and binders on material properties and molding parameters in iron and stainless steel powder injection molding process

It is essential to study and optimize multiple objective functions such as binder system design, feedstock, part geometry, mold design, and processing conditions in order to develop a successful powder injection molding process. A powder with different combinations of binder systems and a binder system with different combinations of powder systems were investigated with a combined experimental and simulation study. First, an experimental rheological study was performed to evaluate the influence of the powder/binder combinations on the rheological behavior and thermal stability of carbonyl iron and stainless steel powder injection molding (PIM) feedstocks. Second, based on the characterization of the feedstock, the simulation study revealed that the pressure-related parameters such as wall shear stress, injection pressure, and clamping force were mainly dependent on the binder system and not much on the powder characteristics, in the range of particle attributes studied. Third, to the temperature-related parameters such as melt front temperature difference and cooling time, binder selection is more critical than powder selection. Fourth, for the velocity-related parameter, maximum shear rate, the selection of both powder and binder system is critical in control. It is demonstrated that the simulation study is essential in the development stage for successful PIM.