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Constraints on F vs. OH incorporation in synthetic [6]Al-bearing monoclinic amphiboles
被引:17
|作者:
Della Ventura, G
[1
]
Robert, JL
Sergent, J
Hawthorne, FC
Delbove, F
机构:
[1] Univ Calabria, Dipartimento Sci Terra, I-87036 Arcavacata Di Rende, CS, Italy
[2] Univ Orleans, CNRS, ISTO, F-45071 Orleans 2, France
[3] Univ Manitoba, Dept Geol Sci, Winnipeg, MB R3T 2N2, Canada
关键词:
richterite;
pargasite;
EMPA;
cell parameters;
infrared spectroscopy;
OH-F incorporation;
D O I:
10.1127/0935-1221/2001/0013/0841
中图分类号:
P57 [矿物学];
学科分类号:
070901 ;
摘要:
In this work we have systematically replaced OH with F in an amphibole composition intermediate between richterite and pargasite [60% richterite and 40% pargasite in molar proportion; nominal composition Na(Na0.6Ca1.4)(Mg4.6Al0.4)(Si7.2Al0.8)O-22(OH,F)(2)]. Syntheses have been done at 3 kbar P-H2O and 900 degreesC, and for all compositions an assemblage of amphibole plus minor Na-phlogopite has been obtained. Crystal-chemical variations in the amphibole as a function of F have been characterized by a combination of EMPA, X-ray powder diffraction, and infrared spectroscopy. EMPA analyses show that for increasing F in the system (i) the Al-[6] content decreases to 0.13 apfu for the nominal fluorine end-member whereas the Al-[4] content is virtually constant and close to the nominal value; (ii) the fluorine content is systematically lower than expected. The infrared OH-stretching spectra show that those OH-groups locally bonded to (MgMgMg)-Mg-M1-Mg-M1-Mg-M3 configurations are preferentially replaced by F whereas those OH-groups locally bonded to (MgMgAl)-Mg-M1-Mg-M1-Al-M3 configurations are not replaced by F.
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页码:841 / 847
页数:7
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