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坦桑石的矿物学及谱学特征研究
引用本文:赖萌,廖宗廷,杨如增,周征宇,钟倩.坦桑石的矿物学及谱学特征研究[J].光谱学与光谱分析,2018,38(9):2872-2876.
作者姓名:赖萌  廖宗廷  杨如增  周征宇  钟倩
作者单位:1. 同济大学海洋地质国家重点实验室,上海 200092
2. 上海宝石及材料工艺工程技术研究中心,上海 200092
3. 同济大学海洋与地球科学学院,宝石及工艺材料实验室,上海 200092
基金项目:国家自然科学基金项目(41272049), 上海市科委专项基金项目(15DZ2283200, 12DZ2251100)资助
摘    要:对来自坦桑尼亚Merelani地区的坦桑石样品,分别采用电子探针、EMXPLUS型ESR谱仪、同步热分析仪、紫外可见光谱仪以及傅里叶变换红外光谱仪进行了测试与分析。结果表明:坦桑石样品的主要成分为SiO2,Al2O3和CaO,微量成分中V2O5含量相对最多,平均含量为0.36%;坦桑石样品本身不含吸附水,结晶水, 加热至780 ℃附近时,脱失结构水,样品中结构水大约占总质量的2%;ESR实验结果中显示出明显Fe3+和Mn2+的电子顺磁信号;紫外-可见光谱显示,样品在385 nm处出现吸收窄带,575和750 nm处分别出现较为宽缓的吸收;红外光谱测试表明,样品在6 500~9 000 cm-1波段的倍频振动区,基本没有吸收。在4 000~6 500 cm-1波段主要为和频振动,5 956 cm-1附近呈较宽缓的吸收峰,5 413,5 184,4 336和4 046 cm-1处出现较尖锐的吸收峰,主要可能由O-H,矿物内的Si-O,以及空气里面的H2O分子和CO2振动所引起。综合EPMA以及ESR分析结果,蓝-紫色坦桑石颜色可能主要由V3+和V5+共同引起,Fe3+晶体场的d-d电子跃迁、Fe2+→Ti4+的电荷转移辅助致色。

关 键 词:坦桑石  谱学特征  颜色成因  矿物学特征  
收稿时间:2017-04-12

Mineralogical and Spectral Characteristics of Tanzanite
LAI Meng,LIAO Zong-ting,YANG Ru-zeng,ZHOU Zheng-yu,ZHONG Qian.Mineralogical and Spectral Characteristics of Tanzanite[J].Spectroscopy and Spectral Analysis,2018,38(9):2872-2876.
Authors:LAI Meng  LIAO Zong-ting  YANG Ru-zeng  ZHOU Zheng-yu  ZHONG Qian
Institution:1. State Key Laboratory of Marine Geology, Tongji University, Shanghai 200092, China 2. Shanghai Engineering & Technology Research Center for Gem and Materials Technics, Shanghai 200092, China 3. Ocean and Earth Science School, Tongji University, Lab of Gem and Technological Materials, Shanghai 200092, China
Abstract:In this paper, the Tanzanite samples from Merelani Tanzania have been respectively tested and analyzed by electron probe, EMXPLUS ESR spectrometer; SDT, UV VIS spectrometer and Fu Liye transform infrared spectrometer. The results show that: the Tanzanite samples are mainly composed of SiO2, Al2O3 and CaO, V2O5 has the content of 0.36%, which is the most trace components; TG-DTA curves show that there is no absorption water and crystal water in Tanzanite samples, when being heated to 780 ℃, the structural water is lost, the water in the samples is about 2% of the total mass; ESR results shows obvious Fe3+ and Mn2+ electron paramagnetic signal; UV Vis spectra shows that an narrow- band absorption appears at 385 nm while a wide- band absorption appears respectively at 575 and 750 nm; infrared spectra shows that there is no absorption in 6 500~9 000 cm-1 of the Tanzanite samples. The 5 956 cm-1 is a wide absorption peak, and there is a sharp absorption peak respectively at 5 413, 5 184, 4 336, and 4 046 cm-1, which are mainly caused by the O-H, the Si-O within in the minerals as well as H2O and CO2 inside the air environment. Based on the results of EPMA and ESR analysis, the color of blue-violet Tanzanite may be mainly caused by V3+ and V5+, d-d electron transition of the crystal field of Fe3+ and charge transfer of Fe2+ to Ti4+ to assist coloration.
Keywords:Tanzanite  Spectroscopic characteristics  Color genesis  Mineralogical characteristics  
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