Self-diffusion of iron and sulfur in ferrous sulfide.

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Title: Self-diffusion of iron and sulfur in ferrous sulfide.
Authors: Condit, R.1, Hobbins, R.2, Birchenall, C.3
Source: Oxidation of Metals. Dec1974, Vol. 8 Issue 6, p409-455. 47p.
Abstract: By use of radiotracer techniques, the iron self-diffusion coefficient in ferrous sulfide single crystals above 620 K was found to be D = Dδ exp {−[(81±4) + (84±20)δ]/RT} where the exponential units are kJ/mole, D is 1.7± 0.1×10 and 3.0±0.2 × 10 cm sec for diffusion in the a- and c-directions, respectively, and δ is the deviation from stoichiometry as given in the formula, FeS. This is a vacancy diffusion mechanism and is discussed in detail. Below 570 K the coefficient is lower than the values given by this equation because of vacancy ordering. The diffusion coefficient for sulfur is many orders of magnitude smaller than for iron. The significance of the data for the Fe−S reaction and other examples of iron diffusion is discussed. [ABSTRACT FROM AUTHOR]
Copyright of Oxidation of Metals is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Self-diffusion of iron and sulfur in ferrous sulfide.
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  Data: By use of radiotracer techniques, the iron self-diffusion coefficient in ferrous sulfide single crystals above 620 K was found to be D = Dδ exp {−[(81±4) + (84±20)δ]/RT} where the exponential units are kJ/mole, D is 1.7± 0.1×10 and 3.0±0.2 × 10 cm sec for diffusion in the a- and c-directions, respectively, and δ is the deviation from stoichiometry as given in the formula, FeS. This is a vacancy diffusion mechanism and is discussed in detail. Below 570 K the coefficient is lower than the values given by this equation because of vacancy ordering. The diffusion coefficient for sulfur is many orders of magnitude smaller than for iron. The significance of the data for the Fe−S reaction and other examples of iron diffusion is discussed. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Oxidation of Metals is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1007/BF00603390
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        Text: English
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      – TitleFull: Self-diffusion of iron and sulfur in ferrous sulfide.
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              Text: Dec1974
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              Y: 1974
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