Flocculation by very high molecular weight polymers

1996 ◽  
Vol 274 (2) ◽  
pp. 172-177 ◽  
Author(s):  
J. -P. Hsu ◽  
D. -P. Lin
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
High Molecular Weight Polymers ◽  
Very High

Highly Stereospecific Polymerizations of 1,3-Butadiene with Cobalt(II) Pyridyl Bis(imine) Complexes

e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Jae Sung Kim ◽  
Chang-Sik Ha ◽  
Il Kim
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Regular Structure ◽  
Aryl Group ◽  
High Molecular Weight Polymers ◽  
Imine Ligands ◽  
Very High

AbstractA series of prototypical Co(II)-based pyridyl bis(imine) complexes {[2- (ArN=C(Me))2C5H3N]CoCl2} (Ar = 2,6-C6H3Me2, 2,5-C6H3Me2, 2,4-C6H3Me2, 2,3- C6H3Me2) bearing two methyl substituents on each imine aryl group are studied as precatalysts for the homopolymerization of 1,3-butadiene. They showed very high polymerization activities associated with ethylaluminum sesquichloride (EAS) as a cocatalyst. The Co(II) catalysts containing less hindered pyridyl bis(imine) ligands, say [2-(2,3-C6H3Me2N=C(Me))2C5H3N]CoCl2 complex, showed highest activity to give high molecular weight polymers. All catalysts yielded cis-1,4-polybutadienes up to 96.4% with cis-1,4 regular structure.

Determination of Peroxides in Synthetic Rubbers

1945 ◽  
Vol 18 (4) ◽  
pp. 874-876
Author(s):  
Richard F. Robey ◽  
Herbert K. Wiese
Keyword(s):  
Molecular Weight ◽  
Natural Rubber ◽  
Quantitative Determination ◽  
High Molecular Weight ◽  
Active Oxygen ◽  
Lower Molecular Weight ◽  
Synthetic Rubber ◽  
High Molecular Weight Polymers ◽  
Methanol Solutions

Abstract Peroxides are found in synthetic rubbers either as the result of attack by oxygen, usually from the air, or as a residue from polymerization operations employing peroxide catalysts. Because of possible detrimental effects of active oxygen on the properties of the rubber, a method of quantitative determination is needed. The concentration of peroxides in substances of lower molecular weight may be determined with ferrous thiocyanate reagent, either titrimetrically as recommended by Yule and Wilson or colorimetrically as by Young, Vogt, and Nieuwland. Unfortunately, many highly polymeric substances are not soluble in the acetone and methanol solutions employed in these procedures. This is also the case with hydrocarbon monomers, such as butadiene, containing appreciable concentrations of soluble high molecular weight polymers. Bolland, Sundralingam, Sutton and Tristram recommended benzene as a solvent for natural rubber samples and the reagent made up in methanol. However, most synthetic rubbers are not readily soluble even in this combination. The following procedure employs the ferrous thiocyanate reagent in combination with a solvent capable of maintaining considerable concentrations of synthetic rubber in solution. The solvent comprises essentially 20 per cent ethanol in chloroform.

scholarly journals The multiple complexes formed by the interaction of platelet factor 4 with heparin

1980 ◽  
Vol 191 (3) ◽  
pp. 769-776 ◽  
Author(s):  
P E Bock ◽  
M Luscombe ◽  
S E Marshall ◽  
D S Pepper ◽  
J J Holbrook
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Chain Length ◽  
Salt Concentration ◽  
Human Platelet ◽  
Platelet Factor 4 ◽  
High Protein ◽  
Platelet Factor ◽  
The Stability ◽  
Very High

The anisotropy of the fluorescence of dansyl (5-dimethylaminonaphthalene-1- sulphonyl) groups covalently attached to human platelet factor 4 was used to detect the macromolecular compounds formed when the factor was mixed with heparin. At low heparin/protein ratios a very-high-molecular-weight compound (1) was formed that dissociated to give a smaller compound (2) when excess heparin was added. 2. A large complex was also detected as a precipitate that formed at high protein concentrations in chloride buffer. It contained 15.7% (w/w) polysaccharide, equivalent to four or five heparin tetrasaccharide units per protein tetramer. In this complex, more than one molecule of protein binds to each heparin molecule of molecular weight greater than about 6 × 10(3).3. The stability of these complexes varied with pH, salt concentration and the chain length of the heparin. The limit complexes found in excess of the larger heparins consisted of only one heparin molecule per protein tetramer, and the failure to observe complexes with four heparin molecules/protein tetramer is discussed.

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