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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >A model for silicate melt viscosity in the system CaMgSi2O6-CaAl2Si2O8-NaAlSi3O8
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A model for silicate melt viscosity in the system CaMgSi2O6-CaAl2Si2O8-NaAlSi3O8

机译:CaMgSi2O6-CaAl2Si2O8-NaAlSi3O8系统中硅酸盐熔体粘度的模型

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摘要

Five hundred eighty-five viscosity measurements on 40 melt compositions from the ternary system CaMgSi2O6 (Di)-CaAl2Si2O8 (An)-NaAlSi3O8 (Ab) have been compiled to create an experimental database spanning a wide range of temperatures (660-2175 degrees C). The melts within this ternary system show near-Arrhenian to strongly non-Arrhenian properties, and in this regard are comparable to natural melts. The database is used to produce a chemical model for the compositional and temperature dependence of melt viscosity in the Di-An-Ab system. We use the Vogel-Fulcher-Tammann equation (VFT: log eta = A + B/(T - C)) to account for the temperature dependence of melt viscosity. We also assume that all silicate melts converge to a common viscosity at high temperature. Thus, A is independent of composition, and all compositional dependence resides in the parameters B and C. The best estimate for A is -5.06, which implies a high-temperature limit to Viscosity Of 10(-5.06) Pa s. The compositional dependence of B and C is expressed by 12 coefficients (b(i=1,2.6,) C-j=1,C-2..6) representing linear (e.g., b(i=1:3)) and higher order, nonlinear (e.g., b(i=4:6)) contributions. Our results suggest a near-linear compositional dependence for B (< 10% nonlinear) and C (< 7% nonlinear). We use the model to predict model VFT functions and to demonstrate the systematic variations in viscosity due to changes in melt composition. Despite the near linear compositional dependence of B and C, the model reproduces the pronounced nonlinearities shown by the original data, including the crossing of VFT functions for different melt compositions. We also calculate values of T-g for melts across the Di-An-Ab ternary system and show that intermediate melt compositions have T-g values that are depressed by up to 100 degrees C relative to the end-members Di-An-Ab. Our non-Arrhenian viscosity model accurately reproduces the original database, allows for continuous variations in theological properties, and has a demonstrated capacity for extrapolation beyond the original data. Copyright (c) 2005 Elsevier Ltd.
机译:对来自三元系统CaMgSi2O6(Di)-CaAl2Si2O8(An)-NaAlSi3O8(Ab)的40种熔体成分进行的858粘度测量已被创建,以创建一个涵盖广泛温度范围(660-2175摄氏度)的实验数据库。该三元体系中的熔体显示出接近阿累尼至极强的非阿勒尼性质,在这方面与天然熔体相当。该数据库用于为Di-An-Ab系统中熔体粘度的成分和温度相关性生成化学模型。我们使用Vogel-Fulcher-Tammann方程(VFT:log eta = A + B /(T-C))来说明熔体粘度对温度的依赖性。我们还假设所有硅酸盐熔体在高温下会聚到相同的粘度。因此,A与成分无关,并且所有成分相关性都位于参数B和C中。A的最佳估计值为-5.06,这意味着粘度的高温极限为10(-5.06)Pa s。 B和C的成分依赖性由代表线性(例如b(i = 1:3))和更高阶的12个系数(b(i = 1,2.6,)Cj = 1,C-2..6)表示。 ,非线性(例如b(i = 4:6))贡献。我们的结果表明,B(<10%非线性)和C(<7%非线性)具有近乎线性的成分依赖性。我们使用该模型预测模型的VFT功能,并证明由于熔体成分变化而引起的系统粘度变化。尽管B和C的成分组成几乎呈线性关系,但该模型仍能再现原始数据所显示的明显非线性,包括不同熔体成分的VFT函数交叉。我们还计算了整个Di-An-Ab三元体系中熔体的T-g值,表明中间熔体成分的T-g值相对于端基Di-An-Ab降低了100摄氏度。我们的非阿伦尼粘度模型可以精确地复制原始数据库,允许其流变学特性连续变化,并具有超出原始数据的推断能力。版权所有(c)2005 Elsevier Ltd.

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