Oxidation and Antioxidant Action in Rubber Vulcanizates

1954 ◽  
Vol 27 (3) ◽  
pp. 671-687 ◽  
Author(s):  
J. Reid Shelton ◽  
William L. Cox

Abstract The variation of rate of oxygen absorption in the constant rate stage with oxygen concentration involves both a square-root and a first-power term for most rubber vulcanizates, although the latter term may be negligible in some cases. A mechanism of oxidation and antioxidant action has been postulated which is consistent with the observed behavior, and which indicates that the antioxidant may function in at least four ways, some beneficial and some harmful. Direct oxygen attack on the antioxidant may produce radicals capable of initiating oxidation chains. Initiation by this mechanism appears to be more important with amine antioxidants than with phenols. The antioxidant may participate in the propagation stage by a chain-transfer mechanism. While this effect alone for a typical antioxidant would probably have only a small effect on the over-all rate of oxidation, it might also affect in a favorable way the secondary reactions which determine changes in physical properties. Amines also appear to be more inclined to chain transfer than are phenols. Termination by a chain-stopping mechanism is one way in which antioxidants retard oxidation. Phenols appear to be more efficient than amines in this connection. Destruction of peroxide by antioxidant-induced decomposition to stable products reduces initiation by peroxide decomposition, and is thus another important mechanism of antioxidant action. The amines are more efficient than the phenols in this regard, and the presence of carbon black is essential for the amines to exhibit their maximum effectiveness. Carbon black is known to promote the decomposition of peroxide to free radicals, but in the presence of amine antioxidants it also promotes the decomposition to stable products. This dual effect of carbon black results in a reversal of effectiveness of amines and phenols in gum and black stocks. The phenols (which function best as chain stoppers) are more effective in the gum stocks; the amines (which function best by reducing peroxide initiation by directing the decomposition to stable products) are more effective in the black stocks.

1977 ◽  
Vol 9 (1-2) ◽  
pp. 26-32 ◽  
Author(s):  
R. E. Beard

In reference [1] Dr. G. C. Taylor has described a useful advance in the techniques available for verification of outstanding claims estimates when the data provided is the cohort development of numbers and amounts of claims. In this note it is assumed that the numbers relate to settled claims and that the amounts relate to claim payments, so there is an implicit assumption that the pattern of partial payments is constant. If the amounts of settled claims were to be used, there would be a one/one relationship between the numbers and amounts, but the effect of the exogeneous factor would be blurred because the settlements in a year other than the first include partial payments made some time previously, and, by hypothesis, based on different factors. If information relating to partial payments is available the data can be examined for any major fluctuation in the pattern and allowance made accordingly.In paragraph (2) of reference [1] a brief description is given of a standard routine calculation in which the average distribution function of claim payments in time is estimated from the triangle of payments by a chain ladder technique. This distribution function is then used to estimate the expected development of the incomplete cohorts, the implicit assumption being made that the function was stable in time. With a constant rate of inflation the results obtained by this technique were found to be satisfactory but with a rapid increase in the rate of inflation the distribution function changed so that projection led to underestimates of the future claims payments. Various methods of adjusting the projections to allow for the change in the rate of inflation have been investigated, but they all involve an important element of subjective judgment and so far no generally suitable basis for “automatic” verification by this particular technique has been discovered. See however reference [2].


1999 ◽  
Vol 64 (25) ◽  
pp. 9189-9193 ◽  
Author(s):  
Michèle P. Bertrand ◽  
Laurence Feray ◽  
Robert Nouguier ◽  
P. Perfetti

2019 ◽  
Vol 10 (7) ◽  
pp. 885-890 ◽  
Author(s):  
Haiyang Yong ◽  
Yongpeng Miao ◽  
Sigen A ◽  
Dong Quan ◽  
Alojz Ivankovic ◽  
...  

Branched polymers exhibit a unique three-dimensional (3D) molecular architecture and distinctive physical/chemical properties, and thus have been applied in a wide variety of fields.


2019 ◽  
Vol 31 (3) ◽  
pp. 407-414
Author(s):  
Hongxin Wang ◽  
Baijun Liu ◽  
Mingyao Zhang ◽  
Shuai Du ◽  
Gaocheng Wu ◽  
...  

e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Ekaterina R. Gasilova ◽  
Olga G. Zakharova ◽  
Sergey D. Zaitsev ◽  
Yury D. Semchikov

AbstractSelf-assembly of poly(methyl methacrylates) end-capped with -Ge(C6F5)3 groups (PMMA-F) has been studied in a selective solvent (acetone) by means of photon correlation spectroscopy and static light scattering. PMMA-F’s of different molecular weights (MW), were obtained by radical polymerization in the presence of a chain transfer agent, HGe(C6F5)3. At MW>130 000 conformational and hydrodynamic properties of PMMA-F’s is shown to be the same as of PMMA. At MW less than130 000 an aggregation starts: additional fraction of large scatterers appears in PCS. Large aggregates of Rh=200 - 300 nm are likely to be formed by bridged micellar clusters. Presence of large aggregates indicates a super strong segregation limit predicted in the work of Semenov et al.


1977 ◽  
Vol 50 (4) ◽  
pp. 641-649 ◽  
Author(s):  
A. H. Weinstein

Abstract A number of substituted symmetrical dithiodiphenols and related monothio-and trithiodiphenols were prepared and characterized. Some of these dithiodiphenols showed chain transfer activity either in bulk styrene or in emulsion diene polymerizations. The fact that phenolic sulfide units were incorporated into polyisoprene and polybutadiene by use of one of these compounds, 2,2′-dithiobis(6-t-butyl-p-cresol), as chain transfer agent was confirmed by ultraviolet analysis. It was demonstrated that selfresistance to oxidation was incorporated into various diene homo- or copolymers, to varying degree, by use of some of these dithiodiphenols as chain transfer agents, on the basis of oxygen absorption tests on preextracted polymers.


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