HIGH TEMPERATURE CALORIMETRY: II. ATOMIC HEATS OF CHROMIUM, MANGANESE, AND COBALT BETWEEN 0° AND 800 °C.

1950 ◽  
Vol 28a (1) ◽  
pp. 51-59 ◽  
Author(s):  
L. D. Armstrong ◽  
H. Grayson-Smith

The atomic heats of chromium, manganese, and cobalt have been measured up to 800 °C. by the adiabatic method described in Part I of this series. The specific heat of chromium is regular from 0° to 800 °C. The measurements with manganese show the sharp α−β transition at 717 °C., with a latent heat of 450 cal. per mole. Typical supercooling occurs on the reverse transition. Cobalt shows an anomaly due to a gradual transition, which is known to be a change in crystal form. The new data obtained permit a comparative discussion of the atomic heats of the transition metals, chromium to nickel. All these have values Cv > 3R at high temperatures. After allowing for the effects of ferromagnetism, the excess specific heats of cobalt and nickel are accounted for by the conduction electrons. This is not true for chromium and manganese, for which metals there must be some additional source of internal energy. It is tentatively suggested that these two metals may have antiferromagnetic transitions at temperatures above 800 °C.

The experiments recorded in the following pages were begun nearly five years ago, at a time when opinion was still much divided as to the atomic weight of cobalt and nickel. It seemed to me that it would be a step in advance if it could be settled which of the two is the greater, for while perhaps the majority of chemists represented the atomic weight of cobalt as greater than that of nickel, some still assigned to them both the same value, while Mendeleeff did not hesitate to invert the order by making Co = 58·5 and Ni = 59. After taking into account all the best evidence on the subject, it appears certain that the atomic weight of cobalt is greater than that of nickel, but the fact remains that the values differ from each other by an amount which is less than the difference between any other two well established atomic weights, the respective numbers being variously represented by different authorities as follows :— The object of my experiments, however, soon developed into a wider field, for it appeared that the results obtained with these two metals might be made the means of further testing the validity of the law of Dulong and Petit, inasmuch as temperatures at which the specific heats would he determined are not only very remote, hut about equally remote, from the melting points of these two metals. Both metals are now obtainable in a pure state, and after melting and solidification under the same conditions are presumably in the same state of aggregation. Their atomic weights, though not known exactly, are undoubtedly very near together, as are also the densities of the metals and other of their physical properties.


In the Bakerian Lecture for 1900 (‘Phil. Trans.,' A, vol. 194, p. 233) it was shown that the specific heats of very pure cobalt and nickel, when compared at temperatures from 100°C. down to the boiling-point of liquid oxygen, — 182°.5 C., steadily approach each other and together tend towards a least value which is at present unknown. It was thought desirable to increase the number of determinations at successive points on the thermometric scale, and to extend the total range of the experiments so as to afford better data for calculation of the form of the curves. The following is an account of the results obtained.


1971 ◽  
Vol 5 (1) ◽  
pp. 115-121 ◽  
Author(s):  
M. Capitelli ◽  
E. Ficocelli

It is shown that the reported absence of a contribution of electronic excitation on to the total specific heats of helium and nitrogen (10,000–35,000°K, 10−1−10 atm) should be attributed to the presence of compensation effects among the various terms into which the total specific heat can be separated and that these terms are influenced by the electronic contribution.


1950 ◽  
Vol 28a (1) ◽  
pp. 44-50 ◽  
Author(s):  
L. D. Armstrong

In this paper is described a new calorimeter for the measurement of specific heats at high temperatures, by the adiabatic method. The advantage is that the specific heat at a definite temperature can be determined by a measurement taken over a small temperature interval, with a precision of 1% or better, throughout the range 400 °C. to 800 °C. This permits a study of specific heat anomalies in this range.


The specific heats of three paramagnetic salts, neodymium magnesium nitrate, manganous ammonium sulphate and ferric ammonium alum, have been measured at temperatures below 1°K using the method of γ -ray heating. The temperature measurements were made in the first instance in terms of the magnetic susceptibilities of the salts, the relation of the susceptibility to the absolute temperature having been determined for each salt in earlier experiments. The γ -ray heatings gave the specific heat in arbitrary units. The absolute values of the specific heats were found by extrapolating the results of paramagnetic relaxation measurements at higher temperatures. The measured specific heat of neodymium magnesium nitrate is compared with the value calculated from paramagnetic resonance data, and good agreement is found.


1979 ◽  
Vol 20 (10) ◽  
pp. 4012-4017 ◽  
Author(s):  
Rosemary A. MacDonald ◽  
Raymond D. Mountain ◽  
Ramesh C. Shukla

The electrical resistivities of lithium -6 and lithium of natural isotopic composition have been studied between 4°K and room temperature. In addition, their absolute resistivities have been carefully compared at room temperature. These measurements show that the effect of ionic mass on electrical resistivity agrees with simple theoretical predictions, namely, that the properties of the conduction electrons in lithium do not depend on the mass of the ions, and that the characteristic lattice frequencies for the two pure isotopes are in the inverse ratio of the square roots of their ionic masses. A comparison with the specific heat results of Martin (1959, 1960), where the simple theory is found not to hold, indicates the possibility that anharmonic effects are present which affect the specific heat but not the electrical resistivity.


1865 ◽  
Vol 155 ◽  
pp. 71-202 ◽  

I. About the year 1780 it was distinctly proved that the same weights of different bodies require unequal quantities of heat to raise them through the same temperature, or on cooling through the same number of thermometric degrees, give out unequal quantities of heat. It was recognized that for different bodies the unequal quantities of heat, by which the same weights of different bodies are heated through the same range, must be determined as special constants, and considered as characteristic of the individual bodies. This newly discovered property of bodies Wilke designated as their specific heat , while Crawford described it as the comparative heat, or as the capacity of bodies for heat . I will not enter upon the earliest investigations of Black, Irvine, Crawford, and Wilke, with reference to which it may merely be mentioned that they depend essentially on the thermal action produced when bodies of different temperatures are mixed, and that Irvine appears to have been the first to state definitely and correctly in what manner this thermal action (that is, the temperature resulting from the mixture) depends on the original temperature, the weights, and the specific heats of the bodies used for the mixture. Lavoisier and Laplace soon introduced the use of the ice-calorimeter as a method for determining the specific heat of bodies; and J. T. Mayer showed subsequently that this determination can be based on the observation of the times in which different bodies placed under comparable conditions cool to the same extent by radiation. The knowledge of the specific heats of solid and liquid bodies gained during the last century, and in the first sixteen years of the present one, by these various methods, may be left unmentioned. The individual determinations then made were not so accurate that they could be compared with the present ones, nor was any general conclusion drawn in reference to the specific heats of the various bodies. 2. Dulong and Petit’s investigations, the publication of which commenced in 1818, brought into the field more accurate determinations, and a general law. The investigations of the relations between the specific heats of the elements and their atomic weights date from this time, and were afterwards followed by similar investigations into the relations of the specific heats of compound bodies to their composition. In order to give a general view of the results of these investigations, it is desirable to present, for the elements mentioned in the sequel, a synopsis of the atomic weights assumed at different times, and of certain numbers which stand in the closest connexion with these atomic weights.


1982 ◽  
Vol 60 (14) ◽  
pp. 1853-1856 ◽  
Author(s):  
Eva I. Vargha-Butler ◽  
A. Wilhelm Neumann ◽  
Hassan A. Hamza

The specific heats of five polymers were determined by differential scanning calorimetry (DSC) in the temperature range of 300 to 360 K. The measurements were performed with polymers in the form of films, powders, and granules to clarify whether or not DSC specific heat values are dependent on the diminution of the sample. It was found that the specific heats for the bulk and powdered form of the polymer samples are indistinguishable within the error limits, justifying the determination of specific heats of powders by means of DSC.


Sign in / Sign up

Export Citation Format

Share Document