The effect of alkali ionic radius, temperature, and pressure on the solubility of water in MAlSi3O8 melts (M = Li, Na, K, Rb)

Citation
H. Behrens et al., The effect of alkali ionic radius, temperature, and pressure on the solubility of water in MAlSi3O8 melts (M = Li, Na, K, Rb), CHEM GEOL, 174(1-3), 2001, pp. 275-289
Citations number
49
Categorie Soggetti
Earth Sciences
Journal title
CHEMICAL GEOLOGY
ISSN journal
00092541 → ACNP
Volume
174
Issue
1-3
Year of publication
2001
Pages
275 - 289
Database
ISI
SICI code
0009-2541(20010401)174:1-3<275:TEOAIR>2.0.ZU;2-2
Abstract
The solubility of water in melts of alkali feldspar endmember compositions (MAlSi3O8, M = Li, Na, K, Rb) was investigated at temperatures 825-1420 deg reesC and pressures 50-800 MPa. Water contents of isobarically quenched gla sses were determined by Karl-Fischer titration (KFT) and/or by near-infrare d (NIR) spectroscopy. At given P and T conditions, the mole fraction of dissolved water decreases with increasing alkali radius from Li to K. The water solubility differenc es between Li-, Na- and K-feldspar compositions are more pronounced at low than at high temperature, For instance, at 500 MPa, the solubility ratio is 1:0.84:0.71 at 900 degreesC and 1:0.87:0.82 at 1200 degreesC. The trend of a decreasing water solubility with increasing alkali radius, however, does not hold for Rb. Ar 1200 degreesC and 400 and 500 MPa, we found a minimum water solubility for K compared to the other alkali (Li, Na, Rb). This result contrasts with the effect of excess alkali oxide on increasing the water solubility in haplogranitic melts which is according to Dingwell et al. [Dingwell, D.B., Holtz, F., Behrens, H., 1997. The solubility of wat er in peralkaline and peraluminous granitic melts. Am. Mineral. 82, 434-437 ] on a molar equivalent basis the same for Cs, Rb, K, and Na whereas it is smaller for Li. With increasing pressure, the water solubility turns over from a retrograde to a prograde T-dependence at constant pressure. Normalizing the solubilit y by the fugacity of H2O a negative dependence on temperature is observed i n the whole PT range of our experiments indicating regardless of whether OH groups or molecular H2O are the dominating water species in the melt the d issolution enthalpy of water in the melt is positive. The pressure, P-neutral, at which water solubility is independent on T decr eases from 700 +/- 100 MPa for LiAlSi3O8 (water content approximate to 16.5 wt.%) to 500 +/- 50 MPa for Na (water content 11.5 wt.%) to 200 +/- 50 MPa for K (water content 5.2 wt.%). For Rb, quench bubbles indicate P-neutral << 300 MPa. P-neutral might be related to the critical behavior of the sili cate-water system. From the observed trend, we infer that the critical curv es of the MAlSi3O8-H2O system in the investigated pressure range progressiv ely shift towards higher T with decreasing ionic radius of the alkali. (C) 2001 Elsevier Science B.V. All rights reserved.