scholarly journals The law of distribution in the case in which one of the phases possesses mechanical rigidity: Adsorption and occlusion

The term “occlusion” has been applied somewhat indiscriminately to denote the state in which a gas exists in a solid, by which it has been absorbed, or from which it is evolved on heating, and no doubt the term includes phenomena of a totally different character. Similarly, the term “adsorption” is commonly used to differentiate between simple cases of solution and the removal of substances from solutions by solids in contact with them. It is the object of this paper to point out similarities which exist between certain cases, which may be included in these two groups, and to make some suggestions as to the classification of the phenomena. In the first place we may dispose of certain instances in which solids evolve gases when they are heated, the change being irreversible. In 1898 I succeeded in showing that the evolution of such gases as hydrogen and carbon monoxide from minerals on heating did not require the assumption of their previous existence in the minerals at all; hence, there was no need to introduce the term occlusion to explain it. I proved that the gases were produced by the interaction of water vapour and carbon dioxide with such substances as ferrous oxide, the change being followed quantitatively. Later, I put forward an explanation of the evolution of helium from minerals, in which it cannot be supposed to be present in a state of chemical combination. Ramsay and Soddy had shown that helium was one of the products of radio-active change, and had suggested that its presence in the minerals was due to the decay of some radio-active substance which they had formerly contained. This explanation did not, however, account for the retention of the gas in the mineral, and the clue to the solution of this part of the problem was given by Jaquerod’s discovery that helium would pass through the walls of a quartz bulb at a comparatively low temperature, though this material is quite impermeable to it in the cold. It follows that the gas may be present in the mineral in a state of supersaturation, and may remain in that state for an indefinite time, if the temperature is moderately low. When, however, the mineral is heated, the gas can diffuse freely through it, and there is a tendency to establish equilibrium between the two phases.

Author(s):  
R. R. Baker

AbstractFlue-cured Virginia tobacco has been heated in nitrogen and nitrogen/oxygen mixtures under flow conditions, and the rate of formation of carbon monoxide and carbon dioxide has been determined as a function of temperature, heating rate, and proportion of oxygen in the gas. When the tobacco is heated in nitrogen at heating rates comparable to those in a smouldering cigarette, 27 % of the carbon content of the tobacco is converted to carbon oxides. Both carbon oxides show two distinct formation regions: a low-temperature region (about 100°-450°C), and a high-temperature region (about 550°-900°C). These temperature limits are almost identical to those predicted from studies on the combustion coal of a cigarette burning in air. When tobacco, or the carbonaceous residue remaining after the pyrolysis experiments, is heated in nitrogen / oxygen mixtures, the total amount of carbon converted to carbon monoxide and carbon dioxide is independent of heating rate, but the relative proportions of the two oxides are strongly dependent on heating rate. At the lower heating rate, proportionally less carbon monoxide, and more carbon dioxide, is produced. Under oxidation conditions, about 70 % of both carbon oxides formed in the low-temperature region (100°-450°C) are produced by tobacco decomposition reactions, whereas in the high-temperature region about 10-20 % of the carbon monoxide, and 2-9 % of the carbon dioxide, are produced by tobacco decomposition.


1971 ◽  
Vol 49 (2) ◽  
pp. 303-306 ◽  
Author(s):  
Pierre Michaud ◽  
Cyrias Oueixet

The slow combustion of ketene was investigated in the low-temperature range 280–350 °C. It differs from the reaction at higher temperatures chiefly by the presence of peroxides (mostly hydroperoxides) and the absence of methane. The main products: formaldehyde, carbon monoxide, water, and carbon dioxide are the same in both cases. A reaction scheme is proposed, which involves degenerate branching through the decomposition of methyl hydroperoxide: CH3OOH = CH3O• + •OH.


2008 ◽  
Vol 254 (2) ◽  
pp. 218-225 ◽  
Author(s):  
M POLLARD ◽  
B WEINSTOCK ◽  
T BITTERWOLF ◽  
P GRIFFITHS ◽  
A PIERSNEWBERY ◽  
...  

1996 ◽  
Vol 15 (12) ◽  
pp. 2829-2832 ◽  
Author(s):  
Matthew S. Sigman ◽  
Bruce E. Eaton ◽  
Jerald D. Heise ◽  
Clifford P. Kubiak

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