Polymerization kinetics of polyacrylamide gels containing immobilized ph gradients for isoelectric focusing

1984 ◽  
Vol 291 ◽  
pp. 31-42 ◽  
Author(s):  
Pier Giorgio Righetti ◽  
Kristina Ek ◽  
Bengt Bjellqvist
1988 ◽  
Vol 9 (9) ◽  
pp. 497-511 ◽  
Author(s):  
Angelika Kinzkofer-Peresch ◽  
Nikos P. Patestos ◽  
Markus Fauth ◽  
Friedrich Kögel ◽  
Roland Zok ◽  
...  

1973 ◽  
Vol 51 (11) ◽  
pp. 1521-1526 ◽  
Author(s):  
Vera Chlumecka ◽  
P. D'Obrenan ◽  
J. S. Colter

A number of earlier studies of three plaque variants of Mengo virus (designated L-, M-, and S-Mengo), all of which suggested that they differ from one another with respect to surface charge characteristics, prompted an examination of the variants by the technique of isoelectric focusing. Highly purified, radiolabelled virus preparations were subjected to electrofocusing in sucrose-stabilized, pH gradients in the presence of 0.5% Brij 35. The distribution of each variant was found to be bimodal; the average values for the pH's at which the major (75–90% of input virions) and minor peaks were found were as follows: L-Mengo, 8.1 and 4.6; M-Mengo, 4.4 and 6.3; S-Mengo, 4.6 and 6.8 Infectivity assays established that the distributions of plaque-forming units, (p.f.u.) and radioactivity were the same (c.p.m./p.f.u. ratios in the major and minor peaks were essentially identical), and re-electrofocusing of virions from each peak was found to give the same bimodal distribution as did the original preparation. The M- and S- variants were found to migrate more rapidly than L-Mengo during electrophoresis in polyacrylamide gels at pH 8.3. The data arising from the electrofocusing studies are compatible with observations regarding the relative rates of attachment of L-, M-, and S-Mengo to cultured L cells and their relative abilities to hemagglutinate human erythrocytes (type O) at pH 8.0.


1981 ◽  
Vol 2 (5-6) ◽  
pp. 291-295 ◽  
Author(s):  
Pier Giorgio Righetti ◽  
Cecilia Gelfi ◽  
Adriana Bianchi Bosisio

1993 ◽  
Vol 14 (1) ◽  
pp. 583-590 ◽  
Author(s):  
Elisabeth Wenisch ◽  
Patrizia de Besi ◽  
Pier Giorgio Righetti

1981 ◽  
Vol 2 (4) ◽  
pp. 213-219 ◽  
Author(s):  
Cecilia Gelfi ◽  
Pier Giorgio Righetti

1980 ◽  
Vol 45 (9) ◽  
pp. 2391-2399 ◽  
Author(s):  
Miroslav Kašpar ◽  
Jiří Trekoval

The polymerization kinetics of isoprene (2-methyl-1,3-butadiene) in benzene with butyllithium as the initiator was investigated by the gas chromatographic method. After completion of the initial period of the reaction, its order with respect to the initial concentration of initiator is negative at the concentrations of the latter between 0.01 and 0.25 mol/l, and positive at higher concentrations. A reaction scheme has been suggested with respect to the "cross" association of butyllithium and of the "living" oligoisoprene.


1980 ◽  
Vol 45 (12) ◽  
pp. 3338-3346
Author(s):  
Miroslav Kašpar ◽  
Jiří Trekoval

The effect of small additions of 1-octene, butyl ethyl ether and triethylamine on the polymerization kinetics of isoprene (2-methyl-1,3-butadiene) in benzene initiated with butyllithium was investigated by employing the GLC analysis. The addition of 1-octane was reflected only in a shorter induction period of the reaction; the effect on the propagation rate was insignificant. With the increasing amount of butyl ethyl ether, the polymerization rate increases linearly, while the reaction order with respect to the concentration of triethylamine is variable and increases from 0.33 to 0.66 with the increasing concentration of the initiator. For a constant concentration of triethylamine, the reaction order with respect to the initial concentration of the initiator was found to vary considerably, reaching even negative values. A reaction scheme was suggested, taking into account the competition between two different solvates of alkyllithium.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1686
Author(s):  
Andrey Galukhin ◽  
Roman Nosov ◽  
Ilya Nikolaev ◽  
Elena Melnikova ◽  
Daut Islamov ◽  
...  

A new rigid tricyanate ester consisting of seven conjugated aromatic units is synthesized, and its structure is confirmed by X-ray analysis. This ester undergoes thermally stimulated polymerization in a liquid state. Conventional and temperature-modulated differential scanning calorimetry techniques are employed to study the polymerization kinetics. A transition of polymerization from a kinetic- to a diffusion-controlled regime is detected. Kinetic analysis is performed by combining isoconversional and model-based computations. It demonstrates that polymerization in the kinetically controlled regime of the present monomer can be described as a quasi-single-step, auto-catalytic, process. The diffusion contribution is parameterized by the Fournier model. Kinetic analysis is complemented by characterization of thermal properties of the corresponding polymerization product by means of thermogravimetric and thermomechanical analyses. Overall, the obtained experimental results are consistent with our hypothesis about the relation between the rigidity and functionality of the cyanate ester monomer, on the one hand, and its reactivity and glass transition temperature of the corresponding polymer, on the other hand.


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