F and Cl diffusion in phonolitic melts: Influence of the Na/K ratio
Fluorine and chlorine diffusion were measured in two natural phonolitic melts, from Vesuvius (Italy) and from Laacher See (Germany), at 0.5 and 1.0 GPa, between 1250 and 1450 °C at anhydrous conditions and with about 2 and 5 wt.% of dissolved water. The two different starting materials allow us to i...
Saved in:
Published in | Chemical geology Vol. 263; no. 1; pp. 89 - 98 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
15.06.2009
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Fluorine and chlorine diffusion were measured in two natural phonolitic melts, from Vesuvius (Italy) and from Laacher See (Germany), at 0.5 and 1.0 GPa, between 1250 and 1450 °C at anhydrous conditions and with about 2 and 5 wt.% of dissolved water. The two different starting materials allow us to investigate the alkali effect, Na vs. K, on halogen diffusion. One composition was a K-rich (~
10 wt.%) phonolitic melt corresponding to the white pumice phase of the 79 AD eruption of Vesuvius, and the other a Na-rich (~
10 wt.%) phonolitic melt corresponding to most differentiated melt of the 12,000 BC eruption of Laacher See. The diffusion-couple technique in a piston cylinder was used for the experiments. Experiments were performed with only one halogen diffusing and with the simultaneous diffusion of a halogen mixture (F, Cl, Br) in order to evaluate the interactions between the halogens during diffusion. Diffusion coefficients for F range between 2
×
10
−
11
m
2/s at 1250 °C and 7
×
10
−
11
m
2/s at 1450 °C for the Na-rich melt and between 1
×
10
−
11
m
2/s at 1250 °C and 8
×
10
−
11
m
2/s at 1450 °C for the K-rich melt at anhydrous conditions. Diffusion coefficients for Cl range between 2
×
10
−
12
m
2/s at 1250 °C and 1
×
10
−
11
m
2/s at 1450 °C for the Na-rich melt and between 7
×
10
−
12
m
2/s at 1250 °C and 2
×
10
−
11
m
2/s at 1450 °C for the K-rich melt at anhydrous conditions. Fluorine diffusivity is higher than Cl in the Na-rich-phonolitic melt by one order of magnitude, whereas in the K-rich-phonolitic melt F and Cl diffusivities are similar. The effect of water is significant for Cl in both Na-rich and K-rich melts: the addition of water enhances Cl diffusivity by up to one order of magnitude, but water does not significantly affect F diffusion. F and Cl diffusivities always differ from one another in the same phonolitic melt composition. F diffusivities are similar in both compositions. Conversely, Cl diffusion depends upon the dominant alkali. These results evidence that halogen diffusivity may represent a limiting factor for their degassing during rapid syneruptive decompression and vesiculation of H
2O-rich-phonolitic melts. The contrasting volatile diffusivities of F and Cl in silicate melts during magma vesiculation may be a key, controlling factor of the composition of the vapour phase (bubbles) produced. Such diffusion controlled degassing model may explain the absence of F and Cl degassing observed during the 79AD eruption of Vesuvius. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0009-2541 1872-6836 |
DOI: | 10.1016/j.chemgeo.2008.08.018 |