Numerical description of shear viscosity functions of long-chain branched metallocene-catalyzed polyethylenes

2008 ◽  
Vol 151 (1-3) ◽  
pp. 129-135 ◽  
Author(s):  
Florian J. Stadler ◽  
Helmut Münstedt
Keyword(s):  
Shear Viscosity ◽  
Viscosity Functions ◽  
Long Chain

scholarly journals Phenomenological Modelling of Non-Monotonous Shear Viscosity Functions

2004 ◽  
Vol 14 (2) ◽  
pp. 82-88 ◽  
Author(s):  
J. David ◽  
P. Filip
Keyword(s):  
Experimental Data ◽  
Shear Rate ◽  
Phenomenological Models ◽  
Shear Viscosity ◽  
Wide Class ◽  
Extreme Points ◽  
Rheological Behaviour ◽  
Viscosity Functions ◽  
Materials Used ◽  
The Individual

AbstractThe aim of this paper is to present a new phenomenological rheological model suitable for the description of a wide class of viscoelastic fluids. Classical phenomenological models predict the relation shear viscosity vs. shear rate (or shear stress) for shear-thinning (or thickening) materials exhibiting smooth monotonous passage from the first - upper (lower) - Newtonian plateau to the second - lower (upper) - one. However, present state of non-Newtonian materials used in practice (ranging from aqueous surfactant solutions, bituminous materials, associative polymers, polymer thickeners, lacquers and gels, to some special disperse systems, etc.) evokes the need to describe this - for many materials non-monotonous - relation in the corresponding way, i.e. through the sufficiently simple phenomenological model with a moderate number of parameters. A six-parameter model enabling description of not only monotonous but also non-monotonous course of shear viscosity function against shear rate (stress) is proposed including physical characterisation of the parameters. This model describes not only extreme points (maximum or minimum) but also a possible appearance of intermediate Newtonian plateau or its indication. The meaning and influence of the individual six parameters is documented on the experimental data published in the literature. There is a good agreement of the model proposed with many different experimental data representing different rheological behaviour. The applicability of this model for a wide class of viscoelastic materials is its principal advantage over the hitherto published phenomenological models.

A Comparative Rheological Investigation of Natural and Synthetic Cis-1,4 Polyisoprenes and Their Carbon Black Compounds

1982 ◽  
Vol 55 (5) ◽  
pp. 1354-1369 ◽  
Author(s):  
S. Montes ◽  
J. L. White
Keyword(s):  
Carbon Black ◽  
Shear Viscosity ◽  
Capillary Rheometer ◽  
Long Chain Branching ◽  
Rheological Measurements ◽  
Naturally Occurring ◽  
Yield Values ◽  
Constant Shear Rate ◽  
Long Chain ◽  
Transient And Steady State

Abstract A comparative experimental study of the rheological properties of four cis-1,4 polyisoprenes, two naturally occurring and two synthetic, is reported. The two naturally occurring elastomers are from the hevea tree and guayule bush, and the synthetics are produced by alkyl lithium and Ziegler catalysts. Transient and steady state shear viscosity, stress relaxation and elongational stretching experiments were carried out at 100°C. Shear viscosity was measured using creep and constant shear rate modes in a sandwich viscometer as well as with a capillary rheometer. The hevea based elastomer has the highest viscosity and maximum relaxation time. The likeliest reasons for the higher viscosity and memory of the hevea is the presence of large amounts of gel and higher levels of long chain branching than in the other cis-1,4 polyisoprenes. Rheological measurements are also reported for compounds with 0.1 and 0.2 volume loadings of carbon black. Yield values are observed for the 0.2 loading compounds.

Polymer Morphology Revealed by Staining Techniques

1981 ◽  
Vol 39 ◽  
pp. 340-341
Author(s):  
A. C. Reimschuessel ◽  
V. Kramer
Keyword(s):  
Polymer Melt ◽  
Nylon 6 ◽  
Morphological Features ◽  
Negative Staining ◽  
Polymer Morphology ◽  
Crystallizable Polymer ◽  
Staining Techniques ◽  
Long Chain

Staining techniques can be used for either the identification of different polymers or for the differentiation of specific morphological domains within a given polymer. To reveal morphological features in nylon 6, we choose a technique based upon diffusion of the staining agent into accessible regions of the polymer.When a crystallizable polymer - such as nylon 6 - is cooled from the melt, lamellae form by chainfolding of the crystallizing long chain macromolecules. The regions between adjacent lamellae represent the less ordered amorphous domains into which stain can diffuse. In this process the lamellae will be “outlined” by the dense stain, giving rise to contrast comparable to that obtained by “negative” staining techniques.If the cooling of the polymer melt proceeds relatively slowly - as in molding operations - the lamellae are usually arranged in a radial manner. This morphology is referred to as spherulitic.

A theory of contamination in electron microscopes by surface diffusion

1978 ◽  
Vol 36 (1) ◽  
pp. 116-117
Author(s):  
J.T. Fourie
Keyword(s):  
Electron Beam ◽  
Surface Diffusion ◽  
High Vacuum ◽  
Ultra High Vacuum ◽  
Physical Parameters ◽  
Carbon Compounds ◽  
Hydrocarbon Molecules ◽  
Electron Microscopes ◽  
Primary Electrons ◽  
Long Chain

Contamination in electron microscopes can be a serious problem in STEM or in situations where a number of high resolution micrographs are required of the same area in TEM. In modern instruments the environment around the specimen can be made free of the hydrocarbon molecules, which are responsible for contamination, by means of either ultra-high vacuum or cryo-pumping techniques. However, these techniques are not effective against hydrocarbon molecules adsorbed on the specimen surface before or during its introduction into the microscope. The present paper is concerned with a theory of how certain physical parameters can influence the surface diffusion of these adsorbed molecules into the electron beam where they are deposited in the form of long chain carbon compounds by interaction with the primary electrons.

The effects of low-ratio n-6/n-3 PUFA on biomarkers of inflammation: a systematic review and meta-analysis

2021 ◽  
Author(s):  
Yali Wei ◽  
Yan Meng ◽  
Na Li ◽  
Qian Wang ◽  
Liyong Chen
Keyword(s):  
Systematic Review ◽  
Fatty Acid ◽  
Polyunsaturated Fatty Acid ◽  
Meta Analysis ◽  
Chain Polyunsaturated Fatty Acid ◽  
Inflammation Markers ◽  
Pufa Supplementation ◽  
Long Chain

The purpose of the systematic review and meta-analysis was to determine if low-ratio n-6/n-3 long-chain polyunsaturated fatty acid (PUFA) supplementation affects serum inflammation markers based on current studies.

Biophysics (and sociology) of ceramides.

2005 ◽  
Vol 72 ◽  
pp. 177-188 ◽  
Author(s):  
Félix M. Goñi ◽  
F-Xabier Contreras ◽  
L-Ruth Montes ◽  
Jesús Sot ◽  
Alicia Alonso
Keyword(s):  
Cell Biology ◽  
Positive Curvature ◽  
Acyl Chain ◽  
Cell Signalling ◽  
Hexagonal Structure ◽  
Lipid Monolayer ◽  
Flip Flop ◽  
Long Chain ◽  
Bilayer Permeability

In the past decade, the long-neglected ceramides (N-acylsphingosines) have become one of the most attractive lipid molecules in molecular cell biology, because of their involvement in essential structures (stratum corneum) and processes (cell signalling). Most natural ceramides have a long (16-24 C atoms) N-acyl chain, but short N-acyl chain ceramides (two to six C atoms) also exist in Nature, apart from being extensively used in experimentation, because they can be dispersed easily in water. Long-chain ceramides are among the most hydrophobic molecules in Nature, they are totally insoluble in water and they hardly mix with phospholipids in membranes, giving rise to ceramide-enriched domains. In situ enzymic generation, or external addition, of long-chain ceramides in membranes has at least three important effects: (i) the lipid monolayer tendency to adopt a negative curvature, e.g. through a transition to an inverted hexagonal structure, is increased, (ii) bilayer permeability to aqueous solutes is notoriously enhanced, and (iii) transbilayer (flip-flop) lipid motion is promoted. Short-chain ceramides mix much better with phospholipids, promote a positive curvature in lipid monolayers, and their capacities to increase bilayer permeability or transbilayer motion are very low or non-existent.

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