首页> 外文期刊>Contributions to Mineralogy and Petrology >Solubility of niobium in the system CaCO3–CaF2–NaNbO3 at 0.1 GPa pressure: implications for the crystallization of pyrochlore from carbonatite magma
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Solubility of niobium in the system CaCO3–CaF2–NaNbO3 at 0.1 GPa pressure: implications for the crystallization of pyrochlore from carbonatite magma

机译:铌在0.1 GPa压力下在CaCO3 –CaF2 –NaNbO3 系统中的溶解度:对碳酸盐岩浆中烧绿石结晶的影响

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摘要

Experimental data are presented for the solubility of NaNbO3 in the ternary system CaCO3–CaF2–NaNbO3 (or calcite–fluorite–lueshite) over the temperature range 500–1,000°C at 0.1 GPa pressure. Liquidus to solidus phase relationships are given for the pseudo-binary join ([CaCO3]60[CaF2]40)100-x –(NaNbO3) x (0 in these liquids is about 17 wt% (or 13.8 wt% Nb2O5) at approximately 930°C, and is represented by the appearance of pyrochlore as the primary liquidus phase. The sub-liquidus assemblages with decreasing temperature for NaNbO3 contents of 20–50 wt% are: pyrochlore + liquid; pyrochlore + CaF2 + liquid; pyrochlore + CaF2 + CaCO3 + liquid. The solidus assemblage is pyrochlore + CaF2 + CaCO3 at temperatures of approximately 700°C (20 wt% NaNbO3) and 600°C (40 wt% NaNbO3). NaNbO3 is present only in sub-solidus assemblages. These data show that in this fluorine-bearing anhydrous system pyrochlore is the principal Nb-hosting supra-solidus phase, in contrast to fluorine-free hydrous melts from which perovskite-structured compounds crystallize. The crystallization of pyrochlore and/or perovskite-structured compounds from haplocarbonatite liquids is thus considered to be dependent upon the F/OH ratio of the melt.
机译:实验数据显示了NaNbO3 在三元体系CaCO3–CaF2 –NaNbO3 (或方解石–萤石–褐铁矿)在500–1,000°的温度范围内的溶解度C在0.1 GPa压力下。给出了伪二元连接([CaCO3 ] 60 [CaF2 ] 40 )100-x –(NaNbO3 < / sub>)x (0 在这些液体中的最大溶解度在大约930°C时约为17 wt%(或13.8 wt%Nb2 O5 ),并以烧绿石为主要液相线。 NaNbO3 含量为20-50 wt%时,温度降低的亚液相线组合为:烧绿石+液体;烧绿石+ CaF2 +液体;烧绿石+ CaF2 + CaCO3 +液体。在约700°C(20 wt%NaNbO3 )和600°C(40 wt%NaNbO3 )的温度下,固相线组合为烧绿石+ CaF2 + CaCO3 。 NaNbO3 仅以亚固相线形式存在。这些数据表明,在该含氟无水体系中,烧绿石是主要的Nb承载超固相,这与钙钛矿结构化合物从中结晶出来的无氟含水熔体相反。因此认为从单碳沸石液体中烧绿石和/或钙钛矿结构的化合物的结晶取决于熔体的F / OH比。

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