Search results for "Viscosity."
showing 10 items of 537 documents
Effect of over the counter mouthwashes with and without alcohol on sorption and solubility of bulk fill resins
2020
Background Composites sorption and solubility can be precursors of several chemical and physical processes, which lead to deleterious effects on the polymer structure. This study evaluated the effect of mouthwashes with and without alcohol on the sorption and solubility of conventional and low viscosity bulk fill resins. Material and Methods Four types of Bulk Fill resins (Filtek™ Bulk Fill, X-tra Fil, Filtek™ Bulk Fill Flow and X-tra Base) were submitted to the following mouthwashes: Listerine Cool Mint and Periogard (containing alcohol) and Listerine Zero and Periogard (alcohol-free). The specimens were stored in the mouthwashes for seven days. Solubility and sorption tests were performed…
Processing and properties of blends with liquid crystal polymers
1990
Experimental data on the processing behavior and on the rheological and mechanical properties of blends with a liquid crystal polymer as one component are presented. The blends with low amounts of LCP show easier processability and lower viscosity than the thermoplastic matrix. The elastic modulus is also improved. The reduction of viscosity has been attributed to the lower pressure entry, due to the formation of fibrils and to the immiscibility of the two phases.
A simplified description of viscoelastic behavior of polymers as illustrated with biaxially-oriented poly(ethylene terephthalate)
1978
A rheological model of solid polymers is proposed. Its mechanical analog is a parallel of a linear spring and a Maxwell element with variable viscosity. The viscosity of the dashpot is allowed to change with stress both directly, by an Eyring-type mechanism, and through free volume changes according to the Doolittle equation. Predictions of the model reproduce many of the features shown, especially after yielding, by constant velocity stress-strain, stress-relaxation and creep data taken at room temperature on biaxially-oriented poly(ethylene terephthalate) over a wide range of loading rates.
Characterization of monopolymer blend of virgin and recycled polyamide 6
2002
It is a common industrial practice to blend virgin polymer with the same recycled polymer coming from plastic scraps that, in general, has not undergone relevant degradation. In this work, the characteristics of blends of virgin and recycled polyamide have been considered by changing the amount of recycled polymer and the presence of humidity and a stabilizer. Neither dry nor wet stabilized recycled polyamide samples show significant variations of the molecular weight, but the melt Newtonian viscosity of the blends are slightly different from that predicted by an additive rule, despite the same chemical nature of the two components. This holds true even more for the humid unstabilized sampl…
Extension of the Concept of Intrinsic Viscosities to Arbitrary Polymer Concentration: From [η] via {η} to Intrinsic Bulkiness
2019
The capabilities of an alternative definition of intrinsic viscosities [η] published some years ago is being studied by means of comprehensive viscometric data reported in the early days of polymer science. It introduces the generalized intrinsic viscosity {η} as the specific hydrodynamic volume at arbitrary polymer concentration c. {η} quantifies the size of the flow unit and decreases monotonously for T ≫ Tg (glass transition temperature) as a function of c but passes a pronounced minimum as T approaches Tg. In the limit of the pure polymer melt, {η} becomes ; this newly introduced property is termed intrinsic bulkiness, by analogy to the intrinsic viscosity, and provides noncalorimetric …
Excess viscosity and glass transition
2001
Abstract Literature data on the viscosity of solutions of poly(butyl methacrylate) (PBMA) and poly(methyl methacrylate) (PMMA) in diethyl phthalate (DEP) for different temperatures, including the range around and below T g , the glass transition temperatures of the pure polymers, were evaluated by means of an approach that uses surface fractions as composition variables. The discussion of these results together with information on solutions of the isomeric polymers, poly(vinyl acetate) (PVAc) and poly(methyl acrylate) (PM(A)), in the same solvent testifies that the previously published relations remain valid for T T g . They enable the determination of viscosities of the pure polymers below…
Interpolymer complexes and polymer compatibility.
2012
A reliable method to decide whether two polymers A and B are miscible or incompatible would be very helpful in many ways. In this contribution we demonstrate why traditional procedures cannot work. We propose to use the intrinsic viscosities [η] of the polymer blends instead of the composition dependence of the viscosities as a criterion for polymer miscibility. Two macromolecules A and B are miscible because of sufficiently favorable interactions between the two types of polymer segments. For solutions of these polymers in a joint solvent, this Gibbs energetic preference of dissimilar intersegmental contacts should prevail upon dilution and lead to the formation of interpolymer complexes, …
Rheological behavior and thermal stability of poly(phenylene sulfide)/vectra-B950 blends
1994
Blends of polyphenylene sulfide (PPS) with a commercial, wholly aromatic, liquid crystalline polymer (LCP), Vectra-B950, have been prepared by melt-blending. Their rheological behavior has been studied in order to determine if the LCP displays a processing aid ability, and under what conditions it gives rise to potentially reinforcing fibrils dispersed in the PPS matrix. The problem of the thermal stability of PPS/LCP blends, which has been considered by some authors as the main obstacle to the production of usable materials due to the evolution of gaseous substances during processing, has been discussed. © 1994 John Wiley & Sons, Inc.
Rheological behavior of a semirigid liquid crystal polymer
1993
The rheological behavior of liquid crystal polymers is still far from completely clarified from both experimental and theoretical points of view. In this paper, the shear flow and the non-isothermal elongation flow behavior of a semi-rigid liquid crystal copolyester is discussed. The viscosity strongly decreases when the test temperature is increased above the crystal-nematic transition temperature; below this temperature the viscosity is very high. The thermal history strongly affects the shear viscosity. The elongational flow behavior depends also on temperature. Above the crystal-nematic transition temperature and the mesophase is easily spinnable, whereas below this temperature, the spi…
Prediction of the flow curves of thermoplastic polymer/clay systems from torque data
2014
Abstract The aim of this work was to determine some relevant rheological parameters of polymer/clay systems using mixing torque and mixing speed data obtained during processing in an internal mixer. The method used was originally proposed by Marquez et al. for monophase polymers, and is here applied to polymer/clay systems for the first time. Several clay-containing composites based on different polymer matrices (i.e., LDPE, HDPE, PA6, EVA) were used to verify the effectiveness of the method for measuring the flow curves of these polymer/clay systems. The results indicated that, for all the systems at low clay level, the rheological curves calculated with the Marquez method fit quite well t…