Crystallinity of silica gel revealed on the heat capacity curve at moderately higher temperature

1958 ◽  
Vol 157 (1) ◽  
pp. 11-16 ◽  
Author(s):  
Tsutomu Takamura
2004 ◽  
Vol 68 (3) ◽  
pp. 515-522 ◽  
Author(s):  
S. Klemme ◽  
J. C. van Miltenburg

AbstractThe low-temperature heat capacity of zinc chromite (ZnCr2O4) was measured between 6.5 K and 400 K using adiabatic calorimetry, and some thermochemical functions (CP(T),S(T), S°298,H(T)-H(0)) were derived from the results. The standard entropy (S°298= 128.6±0.3 J mol-1K-1) for zinc chromite was calculated from the results. Our calorimetric measurements indicate one extremely large anomaly in the heat capacity curve at ∼12.3 K which is related to the cubic-tetragonal transition in ZnCr2O4.


1932 ◽  
Vol 7 (6) ◽  
pp. 677-679 ◽  
Author(s):  
W. F. Hampton ◽  
J. H. Mennie

The heat capacity of Monel metal over the range − 183° to 25 °C. has been measured in an adiabatic calorimeter. By differentiation of the equation representing the heat capacity curve, an equation for the specific heat over this range is obtained and values at various temperatures calculated. The specific heat at 20 °C. is found to be 0.0997.


2020 ◽  
Vol 22 (19) ◽  
pp. 10882-10892
Author(s):  
M. N. Guimarães ◽  
M. M. de Almeida ◽  
J. M. C. Marques ◽  
F. V. Prudente

Parallel tempering Monte Carlo calculations on the Li+Arn microsolvation clusters have shown that the two peaks appearing in the heat capacity curve as a function of temperature correspond to the melting of the second and first solvation shells.


The original object of the present research was to investigate the sorption of methyl alcohol by silica gel, in order to compare the isothermals with those of water and ethyl alcohol, which had been determined by Lambert and Foster. Owing to the fact that the supply of gel used for this earlier work had been exhausted, it as necessary to examine a number of other specimens. One of these, which like the original gel, was a commercial product, was found to take up a larger amount at saturation, and also to exhibit hysteresis phenomena which were not observed with the original gel. Unfortunately it was impossible to find a sample giving exactly the same shape of isothermal as the original gel, although some specimens known to belong to the same batch gave very similar curves. One of these was selected for the present work, and an examination has been made of the isothermals of methyl and ethyl alcohols on these two types of silica gel at 25° C. The fact that one specimen showed hysteresis provided a suitable occasion further to confirm the view, always maintained by Lambert and the author, that these phenomena are in no way due to incomplete removal of permanent gases or other impurities from the systems. In previous work with silica and ferric oxide gels, evacuation was carried out at 150° C, which is actually the optimum temperatures of activation for the latter gel, the adsorptive capacity of which decreases rapidly when higher temperatures are employed. Silica gels, however, will withstand a much higher temperature with comparatively little diminution in capacity, and in the present work it has been shown that the hysteresis phenomena are not affected by raising the temperature of the initial evacuation to 250° C or even to 350° C. It has also been shown that the phenomena persist after continued "flushing out" of the gel with methyl or ethyl alcohol vapour. (McBain suggested that the hysteresis observed by Lambert and Clark with benzene on ferric oxide gel would not have ocucrred if the gel had been flushed out with benzene before the isothermals were determined.)


1984 ◽  
Vol 32 ◽  
Author(s):  
R. K. Brow ◽  
C. G. Pantano

ABSTRACTSol/gel derived silica thin films were thermally treated in NH3 for four hours at temperatures up to 1300C. The films were analyzed by ellipsometry, X-ray photoelectron spectroscopy (XPS) and infrared spectroscopy (IR). Over 30 mol% nitrogen was incorporated in the film treated at 1300C. Using IR and XPS analyses, -NHx groups were found to be present after low temperature treatments, while nitrogen was incorporated in an oxynitride structure after the higher temperature treatments.


1987 ◽  
Vol 26 (S3-1) ◽  
pp. 283 ◽  
Author(s):  
D. Finotello ◽  
A. Wong ◽  
K. A. Gillis ◽  
D. D. Awschalom ◽  
M. H. W. Chan

1959 ◽  
Vol 32 (4) ◽  
pp. 1020-1026
Author(s):  
M. P. Votinov ◽  
L. L. Sulzhenko ◽  
E. V. Kuvshinskiĭ

Abstract 1. The initial stages of stretching of natural rubber gum compounds ((λ≦4.5)) and of filled compounds ((λ=1.8−4)) are characterized by liberation of heat equivalent to the work of deformation according to Equation (lb). Further deformation takes place with liberation of surplus heat caused by- crystallization of the rubber. The relation between the work of deformation and the heat effect is given by Equation (1a) 2. The beginning of crystallization and its degree at a given elongation depend on the degree of vulcanization and on the nature of the dispersed fillers. The rubbers with the highest modulus crystallize the poorest. Active fillers such as channel black promote crystallization to a greater degree than silica gel and chalk. 3. A rate of deformation of 100% per second assures adiabatic conditions without taking special measures. 4. It was determined that errors in the quantitative analysis of the process of adiabatic stretching of rubbers result from lack of knowledge of the true heat capacity of the compound and especially from inaccuracy of measurement of elongation during the relaxation cycle.


1953 ◽  
Vol 1 (4) ◽  
pp. 164-169 ◽  
Author(s):  
S. Paterson

AbstractAn infinite or semi-infinite medium, in which heat is generated or absorbed at a rate proportional to the temperature, is placed at temperature zero in contact with a perfect conductor of finite heat capacity at a higher temperature. Expressions are derived for the subsequent behaviour in linear and spherical cases, and applications suggested.


2017 ◽  
Vol 20 (9) ◽  
pp. 859-863
Author(s):  
Joselma A. Amorim ◽  
I. C. A. Brito ◽  
H. M. Vieira ◽  
P. J. Vodianitskaia ◽  
Jose Mauricio Gurgel

2010 ◽  
Vol 103 (2) ◽  
pp. 773-778 ◽  
Author(s):  
Yuri I. Aristov ◽  
Yulia A. Kovalevskaya ◽  
Michael M. Tokarev ◽  
Igor E. Paukov

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