Rubber Elasticity Study of Polyurethane Networks Prepared by Cyclotrimerisation Crosslinking Reaction of Isocyanate Groups

2007 ◽  
Vol 555 ◽  
pp. 491-496 ◽  
Author(s):  
J. Budinski-Simendić ◽  
M. Ilavsky ◽  
Jan Šomvarsky ◽  
M. Špírková ◽  
Lj. Korugić-Karasz ◽  
...  

The aim of this contribution was to study the rubber elasticity of dry and swollen networks obtained by cyclotrimerization crosslinking reaction of isocyanate groups located at a linear telechelic network precursor. Telechelic diisocyanates were prepared in the undiluted state from 2,4-tolylene diisocyanate, α,ω,dihydroxypoly(oxypropylenes) and different contents of the monool component 2-(2-metoxyetoxy) ethanol. The network synthesis proceeded in a bulk. Detailed network topology was calculated by the theory of branching processes. The equilibrium swelling degree of prepared samples was related to the parameters, which are experimentally accessible for a network arising from an end-linking process using the Flory-Rehner theory. The experimental data for network modulus were compared with those arising from the "affine" model, "phantom’ model" and the model of constrained junctions.

1966 ◽  
Vol 39 (5) ◽  
pp. 1472-1488 ◽  
Author(s):  
G. R. Dobson ◽  
M. Gordon

Abstract Recent efforts to reformulate statistical theories of polymeric systems in terms of the theory of branching (“cascade”) processes, are here extended to calculations of statistical parameters for the theory of rubber elasticity, viz., the number and mean length of various forms of active network chains. New simple results are given for random ƒ-functional polycondensation; it is shown that such systems are of interest in rubber elasticity studies in the region just after the gel point, where the concentration of active network chains varies rapidly with conversion, while the mean length of these chains diverges at the gel point. General exact formulas are derived for random crosslinking of arbitrary primary distributions, without assuming that the mean primary chain length is necessarily large; examples are worked out for uniform (homodisperse) chains, random, self-convoluted random, or Poisson primary distributions. Calculations are extended also to the cross-polymerization type of vulcanization reaction attributed to the cure of polybutadiene with peroxides. The results suggest reasons for differences in technical performance observed with such rubbers.


1958 ◽  
Vol 31 (1) ◽  
pp. 117-131 ◽  
Author(s):  
O. Lorenz ◽  
Elisabeth Echte

Abstract The vulcanization of natural rubber with sulfur, using mercaptobenzothiazole as accelerator in the presence of zinc stearate, was investigated. The results were as follows: 1) When natural rubber is cured with sulfur in the presence of zinc oxide and mercaptobenzothiazole, as well as zinc stearate, one observes, with the first order diminution of sulfur concentration, an induction period that grows longer as the cure temperature falls. 2) For the disappearance of sulfur there is calculated, from the temperature dependence of the rate constants, an activation energy of 19.5 kcal/mole. This value is considerably smaller than that found for the mercaptobenzothiazole-accelerated sulfur cure when no zinc stearate is present. 3) The percentage loss in mercaptobenzothiazole during vulcanization is, in the presence of zinc stearate, independent of the temperature; there is a reaction, independent of the amount of stearate added of 5 molecules of S8 for each molecule of mercaptobenzothiazole. 4) The diminution in accelerator can also be explained as a first order reaction, and it becomes evident that disappearance of accelerator and sulfur are equivalent-rate processes. 5) The crosslinking, measured by the reciprocal equilibrium swelling, goes according to the first order, yet sulfur disappearance and the crosslinking reaction are not equal rate processes, which was always true in the absence of zinc stearate. In each case the crosslinking rate constants are greater than those for the decrease in sulfur. 6) For the activation energy of network formation, we calculated, from the temperature dependence of the rate constants of the reciprocal equilibrium swelling, 20.5 kcal/mole. 7) When the stearate content is constant, there is a linear relationship between kSI, the rate constant for sulfur diminution, and the given amount of mercaptobenzothiazole, up to an initial molar ratio of mercaptobenzothiazole: stearate = 4:1. Increases in accelerator proportion beyond this initial ratio cause no further rise in the rate constants. 8) The rate constants of the crosslinking reaction also increase with increasing proportion of mercaptobenzothiazole (stearate portion remaining constant), until the initial molar ratio of mercaptobenzothiazole:zinc stearate = 4:1 is reached. Nevertheless, the relationship is not linear. 9) There is a linear relationship between the amount of zinc stearate in the vulcanizate and the maximum sulfur-loss rate constants kSI (max). 10) The maximum rate constants of the network forming reaction kQI (max) are proportional to the square root of the stearate content. 11) The number of crosslinkage points formed is independent of the quantity of mercaptobenzothiazole, when the stearate content is constant. 12) The number of crosslinking points formed increases, however, along with increasing stearate content, and is proportional to the square root of the stearate content. The investigations will be continued.


1965 ◽  
Vol 38 (2) ◽  
pp. 374-378
Author(s):  
L. J. Maisey ◽  
J. Scanlan

Abstract The effect of antioxidant on the crosslinking reaction occurring during the oxidation of sulphur vulcanizates of natural rubber was investigated by using both continuous and intermittent stress relaxation measurements. Similarly, by means of continuous stress relaxation and equilibrium swelling measurements the cross-linking reaction in vacuum was followed. The presence of antioxidant or removal of air reduced considerably both continuous and intermittent relaxation and also the difference between them, which measures the crosslinking. The crosslink formation must therefore form part of the sequence of oxidative reactions.


2006 ◽  
Vol 518 ◽  
pp. 399-404 ◽  
Author(s):  
J. Budinski-Simendić ◽  
M. Špírková ◽  
K. Dušek ◽  
T. Dikić ◽  
R. Radičević ◽  
...  

Here, as part of our experimental investigations dealing with poly(urethane-isocyanurate) networks, we investigate model irregular networks with increasing amount of dangling chains. In our study such an irregular network topology was obtained by partial substitution of a diol for a monohydroxy component during the preparation of isocyanate terminated precursors. Telechelic diisocyanates were synthesized from aromatic diisocyanate (2,4-TDI), α,ω-dihidroxypoly (oxypropylene) (PPG 2000), and diethyleneglycolmonomethylether (an aliphatic low-molecularweight monool component). The networks in undiluted state were prepared by cyclotrimerisation, in the presence of a catalyst. The network properties were estimated by multiple extraction in solvent, differential scanning calorimetry and photoelastical measurements. Independently of mechanical testing, the fraction and concentration of dangling and elastically active network chains were evaluated by the theory of branching processes (cascade theory). The influence of dangling chains on the mechanical properties was analyzed.


2007 ◽  
Vol 44 (02) ◽  
pp. 492-505
Author(s):  
M. Molina ◽  
M. Mota ◽  
A. Ramos

We investigate the probabilistic evolution of a near-critical bisexual branching process with mating depending on the number of couples in the population. We determine sufficient conditions which guarantee either the almost sure extinction of such a process or its survival with positive probability. We also establish some limiting results concerning the sequences of couples, females, and males, suitably normalized. In particular, gamma, normal, and degenerate distributions are proved to be limit laws. The results also hold for bisexual Bienaymé–Galton–Watson processes, and can be adapted to other classes of near-critical bisexual branching processes.


Author(s):  
C. N. Sun

Myoepithelial cells have been observed in the prostate, harderian, apocrine, exocrine sweat and mammary glands. Such cells and their numerous branching processes form basket-like structures around the glandular acini. Their shapes are quite different from structures seen either in spindleshaped smooth muscle cells or skeletal muscle cells. These myoepithelial cells lie on the epithelial side of the basement membrane in the glands. This presentation describes the ultrastructure of such myoepithelial cells which have been found also in the parotid gland carcinoma from a 45-year old patient.Specimens were cut into small pieces about 1 mm3 and immediately fixed in 4 percent glutaraldehyde in phosphate buffer for two hours, then post-fixed in 1 percent buffered osmium tetroxide for 1 hour. After dehydration, tissues were embedded in Epon 812. Thin sections were stained with uranyl acetate and lead citrate. Ultrastructurally, the pattern of each individual cell showed wide variations.


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