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首页> 外文期刊>The American mineralogist >Accurate determination of Fe3+/Sigma Fe of andesitic glass by Mossbauer spectroscopy
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Accurate determination of Fe3+/Sigma Fe of andesitic glass by Mossbauer spectroscopy

机译:Mossbauer光谱法准确测定安山玻璃中Fe3 + / Sigma Fe

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To evaluate the accuracy of Fe3+ and Fe2+ ratios in silicate glasses determined by Mossbauer spectroscopy, we examine in detail the temperature (47-293 K) of Mossbauer spectra for two andesitic glasses, one quenched at 1 atm, 1400 degrees C (VF3) and the other at 3.5 GPa, 1600 degrees C (M544). Variable-temperature Mossbauer spectra of these two glasses are used to characterize the recoilless fraction, f, by two different methods a relative method (RM) based on the temperature dependence of the ratios of Fe3+ and Fe2+ Mossbauer doublets and the second based on the temperature dependence of the center shift (CS) of the doublets. The ratio of the recoilless fractions for Fe3+ and Fe2+, CT, can then be used to adjust the observed area of the Mossbauer doublets into the Fe3+/Sigma Fe ratio in the sample. We also evaluated the contributions of non-paramagnetic components to the Fe in the glasses by determining the influence of applied magnetic field on sample magnetization. Finally, for the VF3 glass, we determined the Fe3+/Sigma Fe independently by wet chemical determination of the FeO content combined with careful electron microprobe analyses of total Fe. Recoilless fractions determined with the CS method (CSM) are significantly smaller than those determined with the relative method and suggest larger corrections to room-temperature Fe3+/Sigma Fe ratios. However, the RM determinations are believed to be more accurate because they depend less on the assumption of the Debye harmonic model and because they produce more nearly temperature-independent estimates of Fe3+/Sigma Fe ratios. Non-linear responses of sample magnetizations to applied magnetic fields indicate that the glasses contain a small (0.4-1.1% for VF3) superparamagnetic component that is most likely to be nanophase precipitates of (Fe,Mg)Fe2O4 oxide, but corrections for this component have negligible influence on the total Fe3+/Sigma Fe determined for the glass. For the VF3 glass, the Fe3+/Sigma Fe produced by uncorrected room-temperature Mossbauer spectroscopy [0.685 +/- 0.014 in two standard deviation (2 sigma)] agrees within 3% of that determined by wet chemistry (0.666 +/- 0.030 in 2 sigma). The Fe3+/Sigma Fe corrected for recoilless fraction contributions is 0.634 +/- 0.078(2 sigma), which is 7.5% lower than the uncorrected room-temperature ratio, but also agrees within 5% of wet chemical ratio. At least for this andesitic glass, the room-temperature determination of Fe3+/Sigma Fe is accurate within analytical uncertainty, but room-temperature Mossbauer determinations of Fe3+/Sigma Fe are always systematically higher compared to recoilless-fraction corrected ratios.
机译:为了评估由Mossbauer光谱法测定的硅酸盐玻璃中Fe3 +和Fe2 +比率的准确性,我们详细检查了两块安山药玻璃的Mossbauer光谱温度(47-293 K),其中一玻璃在1 atm淬火,1400℃(VF3)和另一个温度为1600摄氏度(3.5 GPa)(M544)。这两种玻璃的可变温度Mossbauer光谱用于表征无反冲分数f,通过两种不同的方法,根据Fe3 +和Fe2 + Mossbauer的二重物比率的温度依赖性,使用相对方法(RM),第二种方法基于温度双峰的中心偏移(CS)的依赖性。 Fe3 +和Fe2 +的无反冲组分的比值CT可用于将Mossbauer双重峰的观察面积调整为样品中Fe3 + / Sigma Fe的比例。我们还通过确定施加磁场对样品磁化强度的影响,评估了非顺磁性成分对玻璃中Fe的贡献。最后,对于VF3玻璃,我们通过湿化学法测定FeO含量并结合仔细的总Fe的电子探针分析,独立测定了Fe3 + / Sigma Fe。用CS方法(CSM)测定的无后坐力分数明显小于用相对方法测定的无后坐力分数,并建议对室温Fe3 + / Sigma Fe比值进行较大的校正。但是,RM测定被认为是更准确的,因为它们较少依赖Debye谐波模型的假设,并且它们产生的Fe3 + / Sigma Fe比值几乎与温度无关。样品磁化强度对施加磁场的非线性响应表明,玻璃中含有少量(对于VF3为0.4-1.1%)超顺磁性成分,最有可能是(Fe,Mg)Fe2O4氧化物的纳米相沉淀,但对此成分进行了校正对玻璃中总Fe3 + / Sigma Fe的影响可忽略不计。对于VF3玻璃,未经校正的室温Mossbauer光谱法生成的Fe3 + / Sigma Fe [两个标准偏差(2 sigma)为0.685 +/- 0.014]符合湿化学法测定的Fe3 + / Sigma Fe(0.666 +/- 0.030 in 2 sigma)。经过校正的无反冲组分贡献的Fe3 + / Sigma Fe为0.634 +/- 0.078(2 sigma),比未经校正的室温比率低7.5%,但也与湿化学比率的5%相符。至少对于这种安山玻璃而言,室温Fe3 + / Sigma Fe的测定在分析不确定性范围内是准确的,但与无反冲分数校正后的比值相比,室温Mossbauer测定Fe3 + / Sigma Fe的系统性始终更高。

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