Direct determination of physical properties from continuous orientation distributions

1988 ◽  
Vol 63 (8) ◽  
pp. 2876-2879 ◽  
Author(s):  
H. R. Wenk ◽  
G. C. Johnson ◽  
S. Matthies
1939 ◽  
Vol 12 (2) ◽  
pp. 269-282 ◽  
Author(s):  
H. I. Cramer ◽  
I. J. Sjothun ◽  
L. E. Oneacre

Abstract The ter Meulen method for the direct determination of oxygen has been adapted, with modifications, to the analysis of raw and vulcanized rubbers. Raney nickel has been found to be quite effective as the reducing catalyst and to be satisfactorily resistant to sulfur poisoning. The method has been applied to the study of the aging of vulcanized rubber in the Geer oven and oxygen bomb. From this study the following conclusions may be drawn: (1) The increase in combined oxygen is greater in the oxygen bomb than in the Geer oven. (2) Deterioration of rubber in the oxygen bomb involves oxidation primarily, whereas that occurring in the Geer oven involves not only oxidation but also thermal decomposition followed by volatilization of oxidation products. (3) The effectiveness of an antioxidant in retarding the absorption of oxygen in oxygen-bomb aging agrees well with its ability to maintain the physical properties of the stock in which it is present. (4) The deterioration in physical properties of a rubber stock in the oxygen bomb during the early stages of aging is a linear function of the increase in combined oxygen. For stocks containing antioxidants and diphenylguanidine as the accelerator, an increase in combined oxygen of approximately 1.2% corresponds to a decrease in tensile strength of 50%. (5) The relationship of increase in combined oxygen to decrease in tensile strength seems to be affected not only by antioxidants, but also by accelerators of vulcanization.


1947 ◽  
Vol 20 (1) ◽  
pp. 320-328 ◽  
Author(s):  
C. O. Willits ◽  
M. L. Swain ◽  
C. L. Ogg

Abstract Direct determination of rubber hydrocarbon in crude rubbers and in latices has been generally considered so inaccurate and unreliable that determination of rubber hydrocarbon by difference has been a common practice. The difference method usually suffices in the analysis of products derived from Hevea rubber, in which the nonrubber components have been well characterized or occur in low concentration. In the analysis of natural rubber products obtained from sources other than Hevea, such as guayule, kok-saghyz, and Cryptostegia, the situation is different. The chemical and physical properties of the nonrubber components of such products are largely unknown, and in many cases the nonrubber contaminants are present in excessive amounts, sometimes more than 50 per cent of the total. Since the rubber hydrocarbon analysis usually affords the most reliable means for estimating the rubber content of plants and for following the concentration and purification of rubber by mechanical and chemical processes, it appeared desirable to devise or adapt a method which would permit direct determination of this constituent in the presence of relatively large amounts of natural and added contaminants.


1961 ◽  
Vol 41 (4) ◽  
pp. 380-384 ◽  
Author(s):  
Arthur F. Dratz ◽  
James C. Coberly
Keyword(s):  

2002 ◽  
Vol 721 ◽  
Author(s):  
Monica Sorescu

AbstractWe propose a two-lattice method for direct determination of the recoilless fraction using a single room-temperature transmission Mössbauer measurement. The method is first demonstrated for the case of iron and metallic glass two-foil system and is next generalized for the case of physical mixtures of two powders. We further apply this method to determine the recoilless fraction of hematite and magnetite particles. Finally, we provide direct measurement of the recoilless fraction in nanohematite and nanomagnetite with an average particle size of 19 nm.


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