The nature of color of gem-quality diaspore (“zultanites”) from Turkey

IF 1.6 4区 地球科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY
Michail Taran, Oleksii Vyshnevskyi, Ievgen Naumenko
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引用次数: 0

Abstract

Two samples of natural gem-quality diaspore (“zultanite”) from Turkey and, for comparison, one sample of high-chromium diaspore from Saranovskoye chromite deposit in northern Urals, were studied by optical absorption spectroscopy. In the polarized spectra of “zultanites” there are two broad bands of Cr3+, caused by electronic spin-allowed transitions 4A2g4T2g and 4A2g4T1g, split by a low-symmetry crystal field of Cr3+ in the distorted octahedral structural position of Al3+. The spectral positions of the bands, especially of the former one, are close to that in Cr3+-bearing chrysoberyl (alexandrite), that causes a weak alexandrite-effect in “zultanites”. A few much weaker bands may be assigned to the spin-forbidden electronic transitions of Fe3+, also substituting Al3+ ions in the octahedral positions of the diaspore structure. The origin of a series of relatively narrow absorption bands in near UV-range, appearing on the background of a strong high-energy absorption edge, is not quite clear. A strong pleochroic absorption edge in the IR range is undoubtedly caused by O–H vibrations of hydroxyl groups in the structure of diaspore (α-AlOOH).

来自土耳其的宝石级一水硬石(“祖坦石”)的颜色性质
采用光学吸收光谱法研究了来自土耳其的两种天然宝石级一水硬铝石(“祖钽石”)样品和来自乌拉尔北部Saranovskoye铬铁矿床的一种高铬一水硬铝石样品。在“zultanites”的极化光谱中,Cr3+的两个宽频带是由电子自旋允许跃迁4A2g→4T2g和4A2g→4T1g引起的,由Cr3+在Al3+扭曲的八面体结构位置上的低对称性晶体场分裂而成。这些条带的光谱位置,特别是前者与含Cr3+的绿绿宝石(亚历山大变石)的光谱位置接近,这导致“绿绿石”具有弱的亚历山大变石效应。一些较弱的能带可以分配给Fe3+的自旋禁止电子跃迁,也取代了Al3+离子在一水硬铝石结构的八面体位置。在近紫外范围内出现的一系列相对狭窄的吸收带,出现在强高能吸收边缘的背景上,其起源并不十分清楚。一水硬铝石(α-AlOOH)结构中羟基的O-H振动无疑是其在红外光谱范围内强多时性吸收的原因。
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来源期刊
Physics and Chemistry of Minerals
Physics and Chemistry of Minerals 地学-材料科学:综合
CiteScore
2.90
自引率
14.30%
发文量
43
审稿时长
3 months
期刊介绍: Physics and Chemistry of Minerals is an international journal devoted to publishing articles and short communications of physical or chemical studies on minerals or solids related to minerals. The aim of the journal is to support competent interdisciplinary work in mineralogy and physics or chemistry. Particular emphasis is placed on applications of modern techniques or new theories and models to interpret atomic structures and physical or chemical properties of minerals. Some subjects of interest are: -Relationships between atomic structure and crystalline state (structures of various states, crystal energies, crystal growth, thermodynamic studies, phase transformations, solid solution, exsolution phenomena, etc.) -General solid state spectroscopy (ultraviolet, visible, infrared, Raman, ESCA, luminescence, X-ray, electron paramagnetic resonance, nuclear magnetic resonance, gamma ray resonance, etc.) -Experimental and theoretical analysis of chemical bonding in minerals (application of crystal field, molecular orbital, band theories, etc.) -Physical properties (magnetic, mechanical, electric, optical, thermodynamic, etc.) -Relations between thermal expansion, compressibility, elastic constants, and fundamental properties of atomic structure, particularly as applied to geophysical problems -Electron microscopy in support of physical and chemical studies -Computational methods in the study of the structure and properties of minerals -Mineral surfaces (experimental methods, structure and properties)
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