Melt fracture,melt viscosities,and die swell of polypropylene resin in capillary flow

The melt fracture, shear viscosity, extensional viscosity, and die swell of a polypropylene resin were studied using a capillary rheometer and dies with a 0.05‐cm diameter and length/radius ratios of 10, 40, and 60. A temperature of 190°C and shear rates between 1 and 5000 s^?1 were used. A modified Bagley plot was used with consideration of pressure effects on both the melt viscosity and end effect. The shear viscosity was calculated from the true wall shear stress. When the true wall shear stress increased, the end effect increased and showed critical stresses at around 0.1 and 0.17 MPa. The extensional viscosity was calculated from the end effect and it showed a decreasing trend when the strain rate increased. Both the shear and extensional viscosities correlated well with another polypropylene reported previously. The die swell was higher for shorter dies and increased when shear stress increased. When the shear rates increased, the extrudate changed from smooth to gross melt fracture with regular patterns (spurt) and then turned into an irregular shape. In the regular stage the wavelength of the extrudates increased when the shear rate increased. The frequency of melt fracture was almost independent of the shear rate, but it decreased slightly when the die length increased. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1587–1594, 2003     

Shear viscosity,extensional viscosity,and die swell of polypropylene in capillary flow with pressure dependency

The shear and extensional viscosities of a polypropylene resin were studied using a capillary rheometer and capillary dies of 1‐mm diameter and length of 10, 20, and 30 mm. Melt temperatures at 190, 205, and 220°C and shear rates between 100 and 5000 s^?1 were used. At the highest shear rate a visible melt fracture was observed. An equation relating the pressure drop and die length was derived with consideration of pressure effects on melt viscosities and the end effect. After the correction for pressure effects the true wall shear stress and end effect at zero pressure were calculated. The end effect showed a critical stress of melt fracture around 10⁵ Pa, and increased rapidly when shear stress increased above the critical stress. From shear stress the shear viscosity was calculated, and a power law behavior was observed. Extensional viscosity was calculated from the end effect and showed a decreasing trend when strain rate increased. After time–temperature superposition shift shear viscosity data correlated well, but an upward trend was observed in extensional viscosity when melt fracture occurred. Die swell ratio at different temperatures can be plotted as a function of wall shear stress and was higher for shorter dies. © 2002 Wiley Perioodicals, Inc. J Appl Polym Sci 84: 1269–1276, 2002; DOI 10.1002/app.10466     

Rheological properties of poly(trimethylene terephthalate) in capillary flow

The shear viscosity, extensional viscosity, and die swell of the PTT melt were investigated using a capillary rheometer. The results showed that the PTT melt was a typical pseudoplastic fluid exhibiting shear thinning and extensional thinning phenomena in capillary flow. There existed no melt fracture phenomenon in the PTT melt through a capillary die even though the shear rate was 20,000 s^?1. Increasing the shear rate would decrease the flow activation energy and decline the sensitivity of the shear viscosity to the melt temperature. The molecular weight had a significant influence on the flow curve. The flow behavior of the PTT melt approached that of Newtonian fluid even though the weight‐molecular weight was below 43,000 s^?1 at 260°C. The extensional viscosity decreased with the increase of the extensional stress, which became more obvious with increasing the molecular weight. The sensitiveness of the extensional viscosity to the melt temperature decreased promptly along with increasing the extensional strain rate. The die swell ratio and end effect would increase along with increasing the shear rate and with decreasing the temperature, which represented that the increase of the shear rate and the decrease of temperature would increase the extruding elasticity of the PTT melt in the capillary die. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 705–709, 2005     

Study on the melt fracture of metallocene poly(ethylene‐octene) in capillary flow

Shear viscosity and melt fracture of a metallocene poly(ethylene‐octene) were studied using a capillary rheometer and dies with different lengths. The true wall shear stresses determined at zero die length showed a dip at high shear rates. The shear viscosity was derived from the true wall shear stress. With increasing shear rates, the extrudate staged from smooth to three types of melt fracture with regular patterns, and then turned into irregular shapes. Three types of regular melt fractures—sharkskin, helix, and spiral (in sequence)—were observed with an increase of the shear rates. The wavelength of the regular melt fracture was measured from extrudates, and the corresponding frequency was calculated. The frequency increased at elevated melt temperatures. Both shear viscosity and frequency at different temperatures correlated well by using the time–temperature Williams–Landel–Ferry (WLF) superposition. Additionally, it was found that the frequency decreased slightly for a longer die but it increased when the shear rate went up. Three frequency functions were associated with three melt fracture patterns, respectively. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 903–911, 2005     

Capillary extrusion behavior of phenolphthalein poly(ether-ether-sulphone) (PES-C)

The capillary extrusion flow properties of novel engineering thermoplastic phenolphthalein poly(ether-ether-sulphone) (PES-C) have been investigated using capillary rheometer. The dependence of viscosity on the wall shear rate and temperatures were obtained. The flow activation energy was found to decrease with shear rate but to be constant with shear stress. The entrance effect was calculated and from which the extensional behavior was estimated using Cogswell's method. From the extrudate swell ratio the principal normal stress was evaluated and a temperature-independent correlation was observed when they were plotted against shear stress. The melt fracture phenomena were checked and discussed also. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65:951–958, 1997     

Melt Flow Properties During Capillary Extrusion of Linear Low-Density Polyethylene

Abstract

The melt flow properties of a linear low-density polyethylene (LLDPE) were measured by means of a capillary rheometer under the experimental conditions of temperatures from 220° to 260°C and apparent shear rates varying from 12 to 120 s^?1. The end pressure drop (ΔP _end) was determined by employing the Bagley's plotting method. The results showed that ΔP _end increased nonlinearly with increasing shear stress. The end pressure fluctuation phenomenon was observed at lower shear stress level, and several plateau regions were generated in the end pressure drop-shear stress curves, suggesting onset of the wall-slip phenomenon during die extrusion of the resin melt. The critical shear stress with onset end pressure fluctuation phenomenon increased with a rise of temperature. Furthermore, the melt shear flow did not strictly obey the power law. The melt shear viscosity decreased nonlinearly with increasing shear stress and with a rise of temperature, whereas the dependence of the melt shear viscosity on the test temperature accorded with a formula similar to the Arrhenius expression.     

The rheology of polysulfone

The viscosity-shear rate functions for polysulfone (PSF) condensates ranging from 0.4RV to 0.95RV were determined using capillary rheometry, The most probable distribution of molecular weights of these resins allowed facile comparison with the polydisperse Bueche theory for viscosity, The agreement in shape of the viscosity function with theory was good but the data were displaced by a factor of 3 to 4 to higher reduced shear rate, a fairly common occurrence for melts. The high absolute value of PSF viscosity was explained with existing empirical correlations as a combination of low critical molecular weight and strong intermolecular interactions. The temperature dependence of viscosity was found to be close to that for polystyrene in the temperature range, T_g + 90 to T_g + 190°C. The die swell, end corrections, and melt fracture characteristics were also determined. The latter was found to occur at a constant wall shear stress of about 6 × 10⁶ dynes/cm² while the die swell and end corrections were found to be small.     

Melt Rheology and Morphology of Nitrile Rubber and Ethylene-Vinyl Acetate Copolymer Blends

The melt Theological behavior of nitrile rubber (NBR)/ethylene-vinyl acetate (EVA) copolymer blends was studied with special reference to the effect of the blend ratio, cross-linking systems, and shear rate using a capillary rheometer. At a given shear stress at 90°C, the viscosities of the blends vary slightly with composition. The effect of cross-linking systems [viz., sulfur (S), peroxide (DCP) and mixed (S+DCP) systems] on the viscosity of NBR/EVA blends is negligible. The melt viscosity of the blends decreases with increasing shear rate, showing pseudoplastic behavior. The flow behavior index values also support the pseudoplastic nature of these blends. Various theoretical models were used to predict the melt viscosity of the blends. Parameters such as die swell, principal normal stress difference, recoverable shear strain, and shear modulus were calculated to characterize the melt elasticity of these blends. The melt elasticity of the system was increased by the addition of NBR to EVA. The extrudate deformation at different shear rates was also studied. It was observed that as the shear rate increases, the extrudate surface exhibits a higher degree of deformation. The morphology of the extrudates of the blends at different shear rates has been examined by a scanning electron microscope. The morphology was found to be dependent on the blend ratio and shear rate.     

Effect of molecular structure on polyethylene melt rheology. III. Effects of long-chain branching and of temperature on melt elasticity in shear

The effects of long-chain branching and of temperature on the melt elasticity in shear of polyethylene were investigated using die swell measurements and relating them to recoverable shear strain, normal stress, and shear modulus. Die swell measurements, as a function of shear rate, were obtained for high- and low-density polyethylenes at temperatures ranging from 130° to 225°C. The samples were characterized by GPC and intrinsic viscosity for molecular weight distributions and degrees of long-chain branching. The importance of annealing the extrudates at temperatures above the polymer melting temperature to achieve equilibrium, or strain-free, values of die swell was demonstrated. The effect of long-chain branch was to decrease elastic deformation. At constant shear stress, the melt elasticity of both high- and low-density polyethylene was found to be essentially independent of temperature. Thus, at constant shear rate, elastic deformation decreased with increasing temperature, and it was demonstrated that this decrease could be quantitatively defined in terms of previously determined shear rate–temperature viscosity superposition shift factors.     

Melt rheological properties of ETFE: an attempt to illuminate the fluorine-substitution effect

Flow behaviors and rheological properties of ethylene tetrafluoroethylene alternating copolymer (ETFE) under high-shear conditions were first reported. Flow instabilities, shear and extensional viscosities, and die swell of ETFE were investigated. Rheological behaviors of perfluorinated ethylene propylene copolymers (FEP), partially fluorinated ETFE, and non-fluorinated polyethylenes (PE) were compared for understanding the role of fluorine incursion on materials properties. It is found that (1) ETFE does not have sharkskin region or second smooth region which frequently occurs in FEP and linear PE; (2) critical shear stresses at which surface melt fracture occurs for the three polymers follow the order: FEP?<?ETFE?<?PE; (3) stable flow region narrows, die swell weakens, and flow activation energy increases when fluorine content of polymer increases. After time?Ctemperature superposition, shifted shear viscosity, extensional viscosity, and elastic data (die swell) present universal scaling characteristic and superpose well in term of the same shift factors.     

Flame retardation of polypropylene: Effect of organoantimony compounds on the melt flow behavior

The melt flow behaviour of polypropylene filled with organoantimony compounds, triphenylstibinedibromide and its derivatives with tribromo-, trichloro-, and pentachloro-phenols, as flame retardants has been studied in the temperature range of 180 to 220°C, and at shear rates of 29.5 to 588.8's^?1, using a capillary rheometer. A decrease in the melt viscosity at all shear rates and temperatures was noticed on addition of these flame retardants, The melt viscosity further decreased upon increasing the concentration (from 5 to 20 phr) of the flame retardants. The die swell was measured in order to determine the melt elasticity of the filled systems. The minimum melt viscosity of filled propylene was observed approximately where the maximum die swell (melt elasticity) occurred.     

Effect of degree of polymerization on gelation and flow processability of poly(vinyl chloride)

The effect of degree of polymerization (DP) on the gelation and flow processability of poly(vinyl chloride) (PVC) was studied. Sheets with adjusted degree of gelation were prepared by rolling rigid pipe formulation suspension PVC compounds with DPs of 800, 1050 and 1300 by changing the milling temperature. Their degrees of gelation were measured with DSC and their capillary flow properties were measured with a capillary rheometer at 150, 170 and 190°C and the effect of DP on the relation between gelation and flow processabilities was studied. Because of the higher shearing heat during milling, the sample with the higher DP had a higher history temperature and thus tended to show a higher degree of gelation. The viscosity increased as the gelation increased. The dependency of viscosity on DP was higher at higher milling and extrusion temperatures and thus at a higher degree of gelation and a lower shear rate. This was assumed to be attributed to the more prominent uniform molecular flow as against the particle flow. The die swell increased with increasing the milling and extrusion temperatures and hence with increasing the gelation. A sample with a lower DP tended to show a larger die swell and this tendency was even more pronounced at the higher extrusion temperature. The melt fracture easily occurred when a sample with advanced gelation was extruded at low temperature. Whereas at low milling temperatures a sample with the lower DP showed a lower critical shear rate at onset of melt fracture, and thus easily generating melt fracture, at high milling temperatures it showed a higher critical shear rate and hence scarcely generated melt fracture. These experimental results were explained by the fact and concept that a sample with a lower DP shows a higher increase in the gelation during extrusion and/or the slighter feature of particle flow as against the uniform molecular flow at the same gelation level. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1915–1938, 2004     

Experimental studies on radial extrudate swell and velocity profiles of flowing PS melt in an electro‐magnetized die of an extrusion rheometer

This article investigates the radial extrudate swell and velocity profiles of polystyrene melt in a capillary die of a constant shear‐rate extrusion rheometer, using a parallel coextrusion technique. An electro‐magnetized capillary die was used to monitor the changes in the radial extrudate swell profiles of the melt, which is relatively novel in polymer processing. The magnetic flux density applied to the capillary die was varied in a parallel direction to the melt flow, and all tests were performed under the critical condition at which sharkskin and melt fracture did not occur in the normal die. The experimental results suggest that the overall extrudate swell for all shear rates increased with increasing magnetic flux density to a maximum value and then decreased at higher densities. The maximum swelling peak of the melt appeared to shift to higher magnetic flux density, and the value of the maximum swell decreased with increasing wall shear rate and die temperature. The effect of magnetic torque on the extrudate swell ratio of PS melt was more pronounced when extruding the melt at low shear rates and low die temperatures. For radial extrudate swell and velocity profiles, the radial swell ratio for a given shear rate decreased with increasing r/R position. There were two regions where the changes in the extrudate swell ratio across the die diameter were obvious with changing magnetic torque and shear rate, one around the duct center and the other around r/R of 0.65–0.85. The changes in the extrudate swell profiles across the die diameter were associated with, and can be explained using, the melt velocity profiles generated during the flow. In summary, the changes in the overall extrudate swell ratio of PS melt in a capillary die were influenced more by the swelling of the melt around the center of the die. Polym. Eng. Sci. 44:2298–2307, 2004. © 2004 Society of Plastics Engineers.     

Effect of molecular weight distribution on the rheological and mechanical properties of polypropylene

The effect of molecular weight distribution on the Theological and mechanical properties of a series of polypropylenes is evaluated. The polypropylenes tested were produced by controlled chemical degradation in a single-screw plasticating extruder. Measured properties include shear, extensional and intrinsic viscosity, melt flow index, extrudate swell, melting and crystallization temperatures, impact strength, flexural modulus, and tensile stress.     

Effects of Extrusion Rate,Temperature, and Die Diameter on Melt Flow Properties During Capillary Flow of Low-Density-Polyethylene

The melt flow properties of a low-density polyethylene were measured at test temperatures varying from 140 to 170°C and in a wide range of extrusion rates by means of a capillary rheometer, to identify the influence of extrusion conditions (such as temperature, shear rate, and die diameter) on the melt flow behavior in the present paper. The results showed that the entry pressure drop increased nonlinearly with an increase of the piston speeds, and it decreased with an addition of the die diameter. The melt shear flow obeyed roughly the power law and the melt shear viscosity decreased approximately linearly with an increase of the true shear rates in a bi-logarithmic coordinate system. The dependence of the melt shear viscosity on temperature accorded approximately the Arrhenius expression. Under these experimental conditions, the entrance pressure drop increases as an exponential function with an addition of the channel contraction ratio.     

Effect of ultrasound on the viscoelasticity and rheology of polystyrene extruded through a slit die

The rheological and processing behavior (melt fracture performance) of polystyrene extruded through a slit die is studied as a function of the ultrasound vibration intensity. The apparent viscosity reduces 29% and die pressure reduces 22% compared with that without ultrasound vibration. The viscosity of the melt decreases exponentially as ultrasound intensity increases and an Arrhenius equation fits the data well. Ultrasound vibration also leads to a decrease of the die swell ratio and a postponement of melts fracture. Characteristic relaxation times at the onset of melt fracture are calculated according to the hypothesis that the melt fracture behavior of a polymer is affected by a balance between its viscous (viscosity) and elastic properties (recoverable shear). Ultrasound vibration shortens the relaxation time of polystyrene molecular chains. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2907–2911, 2006     

A study of extrudate distortion in controlled-rheology polypropylenes

The melt fracture characteristics of controlled-rheology polypropylenes (CRPP) were studied by means of capillary rheometry experiments. CRPPs were produced through reactive extrusion of a commodity polypropylene resin using various peroxide concentrations. These materials exhibited lower molecular weights and narrower molecular weight distributions than those of the starting commodity resin. The CRPP materials studied were found to exhibit only gross melt fracture. At extremely high shear rates and relatively low temperatures, a sigmoidal flexure was observed in the flow curve of certain CRPPs. Generally, it was found that the severity of melt fracture decreased with increasing shear rate for a given material and temperature and in some cases, the extrudates exhibited completely smooth surfaces. Also, the severity of surface distortions was reduced when high L/D dies were employed at a given shear rate. The critical shear stress for the melt fracture onset was found to increase with decreasing molecular weight and polydispersity, and correlations have been developed between the critical stress values and the polymer polydispersity and shear compliance.     

高分子材料动态成型过程中熔体非线性行为的研究

借助流变测量和连续介质理论,不依赖已有的本构关系,对平行叠加正弦振动条件下高分子熔体经毛细管的动态挤出过程进行了理论分析。以低密度聚乙烯(LDPE)为原材料,实验测量LDPE熔体在一定振动频率和振幅下毛细管入口压力、体积流量和挤出胀大的瞬态值,即可得到动态成型过程中高分子熔体剪切应力、剪切速率和表观粘度的变化规律:随振幅和频率的变化,LDPE熔体的表观粘度呈非线性变化趋势;在不同的振幅和频率下动态挤出LDPE熔体,跟稳态挤出时一样,壁面剪切应力与壁面剪切速率也成非线性比例关系。     

Effects of ultrasonic oscillations on rheological behavior and mechanical properties of novel propylene‐based plastomers

The effects of ultrasonic oscillations on the die pressure, productivity of extrusion, melt apparent viscosity, melt surface appearance, and die swell of novel propylene‐based plastomers were studied in a specially designed ultrasonic oscillations extrusion system developed in our laboratory. The effects of ultrasonic oscillations on molecular weights, tensile strength, and dynamic mechanical properties of extrudates were also studied. The experimental results showed that the presence of ultrasonic oscillations during extrusion could significantly increase the productivity of plastomers at the same die pressure, and reduce die swell and melt fracture such as sharkskin at a given screw rotation speed. The die pressure and apparent viscosity of plastomers remarkably decreased with increasing ultrasonic intensity. Introduction of ultrasonic oscillations into plastomer melts can improve their processibility. The possible mechanism for ultrasonic improvement of rheological behavior was also proposed in this article. Under certain conditions, ultrasound‐assisted extrusion could slightly decrease the glass transition temperature (T_g) and storage modulus of plastomers due to the minor reduction in molecular weights, but showed no significant impact on yield strength and strength at break. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007