Reflectance spectra of carbonate minerals in the shortwave infrared (SWIR) and thermal infrared (TIR) wavelength regions contain a number of diagnostic absorption features. The shape of these features depends on various physical and chemical parameters. To accurately identify carbonate minerals or rocks in pure and mixed form, it is necessary to analyze the effects of the parameters on spectral characteristics. In this study, we analyzed spectral absorption feature characteristics of calcite and dolomite in the SWIR (features at 2.3 and 2.5 μm) and TIR (features at 11.5 and 14 μm) wavelength regions, as a function of grain size and carbonate mineral mixtures. Results showed that varying grain sizes and mineral contents in the sample, influence reflectance values and absorption feature characteristics. Absorption band positions of pure and mixed calcite and dolomite in the SWIR and TIR regions for both features were displaced slightly as observed in previous studies. The band positions of calcite and dolomite varied relative to grain size only in the TIR region. These positions shifted to longer wavelengths for the feature at 11.5 μm and to shorter wavelengths for the feature at 14 μm from fine to coarse grain size. The band positions of calcite-dolomite mixtures in the SWIR and TIR regions were determined by the quantity of calcite and dolomite in the sample. These results can be applied for the identification of pure and mixed calcite and dolomite, as well as estimating the relative abundance of both minerals with different grain size and mineral mixtures in a OPEN ACCESS Remote Sens. 2012, 4 988 synthetic sample or rock. They can also be used as a preliminary proxy for assessing dolomitization patterns in carbonate rocks.

The development of advanced laboratory-based imaging hyperspectral sensors, such as SisuCHEMA, has created an opportunity to extract compositional information of mineral mixtures from spectral images. Determining proportions of minerals on rock surfaces based on spectral signature is a challenging approach due to naturally-occurring minerals that exist in the form of intimate mixtures, and grain size variations. This study demonstrates the application of SisuCHEMA hyperspectral data to determine mineral components in hand specimens of carbonate rocks. Here, we applied wavelength position, spectral angle mapper (SAM) and linear spectral unmixing (LSU) approaches to estimate the chemical composition and the relative abundance of carbonate minerals on the rock surfaces. The accuracy of these classification methods and correlation between mineral chemistry and mineral spectral characteristics in determining mineral constituents of rocks are also analyzed. Results showed that chemical composition (Ca-Mg ratio) of carbonate minerals at a pixel (e.g., sub-grain) level can be extracted from the image pixel spectra using these spectral analysis methods. The results also indicated that the spatial distribution and the proportions of calcite-dolomite mixtures on the rock surfaces vary between the spectral methods. For the image shortwave infrared (SWIR) spectra, the wavelength position approach was found to be sensitive to all compositional variations of carbonate mineral mixtures when compared to the SAM and LSU approaches. The correlation between geochemical elements and spectroscopic parameters also revealed the presence of

Shortwave infrared (SWIR) spectroscopy can be applied directly to analyze the mineral chemistry of raw or geologic materials. It provides diagnostic spectral characteristics of the chemical composition of minerals, information that is invaluable for the identification and quality control of such materials. The present study aims to investigate the potential of SWIR spectroscopy as an alternative quality control technique for the mineral chemistry analysis of Portland cement-grade limestone. We used the spectroscopic (wavelength position and depth of absorption feature) and geochemical characteristics of limestone samples to estimate the abundance and composition of carbonate and clay minerals on rock surfaces. The depth of the carbonate (CO 3 ) and Al-OH absorption features are linearly correlated with the contents of CaO and Al 2 O 3 in the samples, respectively, as determined by portable X-ray fluorescence (PXRF) measurements. Variations in the wavelength position of CO 3 and Al-OH absorption features are related to changes in the chemical compositions of the samples. The results showed that the dark gray and light gray limestone samples are better suited for manufacturing Portland cement clinker than the dolomitic limestone samples. This finding is based on the CaO, MgO, Al 2 O 3 , and SiO 2 concentrations and compositions. The results indicate that SWIR spectroscopy is an appropriate approach for the chemical quality control of cement raw materials.