Apparatus for the Direct Determination of the Dynamic Bulk Modulus

1956 ◽  
Vol 27 (5) ◽  
pp. 425-430 ◽  
Author(s):  
John E. McKinney ◽  
Seymour Edelman ◽  
Robert S. Marvin
1957 ◽  
Vol 30 (2) ◽  
pp. 449-459
Author(s):  
J. E. McKinney ◽  
S. Edelman ◽  
R. S. Marvin

Abstract An apparatus has been developed for the direct measurement of the real and imaginary parts of the dynamic bulk modulus of solid and liquid materials over the frequency range of 50 to 10,000 cps. Piezoelectric crystals serving as driver and detector, together with the sample and a confining liquid, are contained in a cavity small compared with the wavelength of sound at these frequencies. Static pressure is superposed to eliminate the effect of small air bubbles. The complex compliances of the sample, confining liquid, and the cavity, are additive in this region, where the compliance is pure dilatation. The dynamic compliances of several natural rubber-sulfur mixtures were obtained in a preliminary evaluation of the behavior of the apparatus.


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.


1996 ◽  
Vol 61 (3) ◽  
pp. 333-341
Author(s):  
Jiří Barek ◽  
Roman Hrnčíř ◽  
Josino C. Moreira ◽  
Jiří Zima

The polarographic behaviour was studied for 6-β-D-glucopyranosyloxy-7-hydroxycoumarin, a natural compound serving as an optical whitening agent. The substance can be quantitated by tast polarography, differential pulse polarography using a conventional dropping mercury electrode, and differential pulse polarography using a static mercury drop electrode over the regions of 20-1 000, 2-1 000, and 0.2-1 000 μmol l-1, respectively. The methods developed for the quantitation of the compound were applied to its direct determination in a raw product.


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