1970
DOI: 10.1080/0002889708506215
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Infrared Spectra for Mineral Identification

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Cited by 39 publications
(35 citation statements)
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“…VNIR-SWIR and IR spectroscopy has been used for qualitative and quantitative analysis for several decades (Taylor et al 1970;Stark et al 1986). Both are based on characteristic vibrations of chemical bonds in molecules, as well as electronic processes (the latter affects only radiation at 400 to 1,000 nm) (Ben-Dor et al 1999).…”
Section: Spectroscopymentioning
confidence: 99%
“…VNIR-SWIR and IR spectroscopy has been used for qualitative and quantitative analysis for several decades (Taylor et al 1970;Stark et al 1986). Both are based on characteristic vibrations of chemical bonds in molecules, as well as electronic processes (the latter affects only radiation at 400 to 1,000 nm) (Ben-Dor et al 1999).…”
Section: Spectroscopymentioning
confidence: 99%
“…In this study, six minerals in Table 1, Kaolinite, Mulite, Muscovite, Pyrophyllite, Montmorillonite and Amorphous silica, were selected as typical interference minerals for investigation. Among the fourteen minerals in the Table, these six minerals are most often quoted as the interference minerals for quartz determination in past IR studies 5,11,13,16,17,[20][21][22][23] . They are commonly used as industrial materials and therefore thought to come into existence in many working environments.…”
Section: Spectrum Measurement Of Interference Mineralsmentioning
confidence: 99%
“…The interference minerals which are known to have a band close to 800 cm -1 are listed in Table 1 5,11,[13][14][15][16][17][18][19][20][21][22][23] . In this study, six minerals in Table 1, Kaolinite, Mulite, Muscovite, Pyrophyllite, Montmorillonite and Amorphous silica, were selected as typical interference minerals for investigation.…”
Section: Spectrum Measurement Of Interference Mineralsmentioning
confidence: 99%
“…IR bands at 3420 and 1640 cm -1 are characteristic for OH molecules (Yamagishi et al, 1997). In addition, all bands under 1080 cm -1 represent chalcedonic quartz components (Taylor et al, 1970;Stockton and Fritsch, 1978). In some published papers (Mc Creery, 2005;Colomban and Prinsloo, 2009), relationship between main bands and vibrational modes of [SiO4] 4-tetrahedron in Raman and IR spectra have been interpreted as follows: Raman active symmetric stretching modes occur between 800 and 1050 cm-1 ; asymmetric IR active stretching between 900 and 1200 cm -1 ; symmetric Raman and IR active bending modes between 400 and 600 cm -1 ; asymmetric IR active bending modes between 500 and 700 cm -1 ; Raman and IR active rotational libration modes about 300 cm -1 ; and Raman and IR active transitional libration modes between 100 and 200 cm -1 (McCreery, 2005;Colomban and Prinsloo, 2009).…”
Section: Discussionmentioning
confidence: 97%