scholarly journals Inverse Emulsion Polymerization for the Synthesis of High Molecular Weight Polyacrylamide and Its Application as Sand Stabilizer

2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
Mahmoud A. Mohsin ◽  
Nuha F. Attia
Keyword(s):  
Molecular Weight ◽  
Emulsion Polymerization ◽  
High Molecular Weight ◽  
Solution Viscosity ◽  
Experimental Conditions ◽  
High Molecular Weight Polymer ◽  
Molecular Weight Polymer ◽  
Inverse Emulsion Polymerization ◽  
Inverse Emulsion ◽  
Molecular Weights

Polyacrylamides constitute a class of polymers that can entirely dissolve or swell in water to form a solution or hydrogel, respectively. Free radical polymerization of acrylamide monomer, using both solution and inverse emulsion polymerization, was applied to produce polyacrylamide with various molecular weights. This investigation was focused on the production of polymers with varying molecular weight, depending on monomer to initiator ratio. Experimental conditions were designed to produce high molecular weight polymers that can be used in stabilization of sand dunes in the arid regions. Synthesized polyacrylamide samples were characterized using Gel Permeation Chromatography and solution viscosity in order to determine the molecular weights and molecular weights distribution. The rheological behavior was also investigated in different polymer concentrations and at various temperatures using Brookfield Rheometer. Lab-scale wind tunnel was used to determine the stability of the sand before and after treatment with the polymer. Compressive stress-strain test was also used to establish the mechanical behavior of the polymer-sand composite under controlled compressive load up to failure. The results showed that the use of high molecular weight polymer gave excellent mechanical and thermal stability.

Experimental Study on Flow-Front Fingering Instabilities in Injection Molding of Polymer Solutions and Melts

2004 ◽  
Author(s):  
Kalonji K. Kabanemi ◽  
Jean-Franc¸ois He´tu ◽  
Samira H. Sammoun
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Polymer Solutions ◽  
Low Molecular Weight ◽  
Flow Front ◽  
High Molecular Weight Polymer ◽  
Molecular Weight Polymer ◽  
Polymer Molecules ◽  
Molecular Weights ◽  
Solvent Molecules

An experimental investigation of the flow behavior of dilute, semi-dilute and concentrated polymer solutions has been carried out to gain a better understanding of the underlying mechanisms leading to the occurrence of instabilities at the advancing flow front during the filling of a mold cavity. Experiments were performed using various mass concentrations of low and high molecular weight polyacrylamide polymers in corn syrup and water. This paper reports a new type of elastic fingering instabilities at the advancing flow front that has been observed only in semi-dilute polymer solutions of high molecular weight polymers. These flow front elastic instabilities seem to arise as a result of a mixture of widely separated high molecular weight polymer molecules and low molecular weight solvent molecules, which gives rise to a largely non-uniform polydisperse solution, with respect to all the kinds of molecules in the resulting mixture (solvent molecules and polymer molecules). The occurrence of these instabilities appears to be independent of the injection flow rate and the cavity thickness. Moreover, these instabilities do not manifest themselves in dilute or concentrated regimes, where respectively, polymer molecules and solvent molecules are minor perturbation of the resulting solution. In those regimes, smooth flow fronts are confirmed from our experiments. Based on these findings, the experimental investigations have been extended to polymer melts. Different mixtures of polycarbonate melts of widely separated molecular weights (low and high molecular weights) were first prepared. The effect of the large polydispersity of the resulting mixtures on the flow front behavior was subsequently studied. The same instabilities at the flow front were observed only in the experiments where a very small amount of high molecular weight polycarbonate polymer has been mixed to a low molecular weight polycarbonate melt (oligomers).

Intrinsic viscoelasticity in thin high-molecular-weight polymer films

2014 ◽  
Vol 89 (6) ◽  
Author(s):  
Xiaoyuan Sheng ◽  
Frédéric Wintzenrieth ◽  
Katherine R. Thomas ◽  
Ullrich Steiner
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Polymer Films ◽  
High Molecular Weight Polymer ◽  
Molecular Weight Polymer

Structural studies of the capsular polysaccharide from Haemophilus pleuropneumoniae serotype 2

1987 ◽  
Vol 65 (5) ◽  
pp. 414-422 ◽  
Author(s):  
Eleonora Altman ◽  
Jean-Robert Brisson ◽  
Malcolm B. Perry
Keyword(s):  
Molecular Weight ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
High Molecular Weight ◽  
Capsular Polysaccharide ◽  
Structural Studies ◽  
High Molecular Weight Polymer ◽  
Molecular Weight Polymer ◽  
Structure Formula ◽  
Nuclear Magnetic

The capsular polysaccharide of Haemophilus pleuropneumoniae serotype 2 (ATCC 27089) is composed of D-glucose (two parts), D-galactose (one part), glycerol (one part), and phosphate (one part). Hydrolysis, dephosphorylation, methylation, enzymic studies, and 1H and 13C nuclear magnetic resonance experiments showed that the polysaccharide is a high molecular weight polymer of a tetrasaccharide repeating units, linked by monophosphate diester and having the following structure:[Formula: see text]

scholarly journals Antigen valence determines the binding of nominal antigen to cytolytic T cell clones.

1985 ◽  
Vol 162 (2) ◽  
pp. 768-773 ◽  
Author(s):  
R F Siliciano ◽  
R M Colello ◽  
A D Keegan ◽  
R Z Dintzis ◽  
H M Dintzis ◽  
...  
Keyword(s):  
Molecular Weight ◽  
T Cell ◽  
High Molecular Weight ◽  
Cytotoxic T Cell ◽  
High Molecular Weight Polymer ◽  
Molecular Weight Polymer ◽  
T Cell Clones ◽  
Cell Clones ◽  
Nominal Antigen ◽  
Epitope Density

We have shown that cytotoxic T cell clones specific for the nominal antigen FL will bind high molecular weight (600,000 to 2,000,000) polyacrylamide and Ficoll polymers conjugated with 200-600 FL groups per molecule. Low molecular weight polymers (40,000) with the same epitope density did not give stable binding. A high molecular weight polymer with a lower epitope density also failed to bind. Taken together, these results suggest that a substantial degree of multivalence is a necessary factor in the stable binding of nominal antigen to T cell clones.

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