Chlorine solubility in silicate melts has been investigated at 830-850 +/- 5-degrees-C and at pressures ranging from 50 to 200 MPa, using both natural (pantellerite, rhyolite, phonolite) and synthetic (SiO2-Al2O3-K2O-Na2O) compositions and a stated H2O-NaCl-KCl fluid phase near 4 molal. At 100 MPa, Cl contents in pantelleritic melts reach a solubility plateau at initial aqueous phase molality near 2. This plateau coincides with a large immiscibility gap between aqueous and chloride-rich fluids. With the coexisting Cl-saturated aqueous phase, Cl ranges from 2720 +/- 120 ppm in rhyolite to 8960 +/- 85 ppm in pantellerite and reaches 6270 +/- 170 ppm in phonolite, at 100 MPa. Between 50 and 200 MPa, the Cl content in pantelleritic melt decreases from 9640 +/- 200 ppm to 5040 +/- 150 ppm. Although Cl solubility increases with increasing FeO* in high SiO2 melts, it is mainly controlled by the Al/Si and (Na + K)/Al molar ratios of the melt with a minimum at Na + K/Al = 1 in a series of synthetic rhyolitic to pantelleritic melts. The experimental results suggest that chlorine occurs as alkali-chloride complexes in high SiO2 melts. They also indicate that Cl is concentrated in the aqueous fluids in equilibrium with SiO2-rich melts, the exact value of D depending on melt composition and melt chlorine concentration. Volcanic degassing will create chlorine-rich hydrothermal fluids and decrease chlorine melt content.
机构:
State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
CAS Center for Excellence in Deep Earth Science, Guangdong, Guangzhou
College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, BeijingState Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
Liu X.
Xu T.
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机构:
State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
CAS Center for Excellence in Deep Earth Science, Guangdong, Guangzhou
College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, BeijingState Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
Xu T.
Xiong X.
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机构:
State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
CAS Center for Excellence in Deep Earth Science, Guangdong, Guangzhou
College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, BeijingState Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
Xiong X.
Li L.
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机构:
State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
CAS Center for Excellence in Deep Earth Science, Guangdong, GuangzhouState Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
Li L.
Wang Y.
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机构:
State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
CAS Center for Excellence in Deep Earth Science, Guangdong, GuangzhouState Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
Wang Y.
Xing C.
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机构:
State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou
CAS Center for Excellence in Deep Earth Science, Guangdong, GuangzhouState Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangdong, Guangzhou