2018
DOI: 10.22606/adap.2018.34004
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Raman and Infrared Spectroscopic Tentative Identification of Organic Traces in Sadiya (LL5) Ordinary Chondrite

Abstract: We report here for the first time the possible presence of organic compounds in Sadiya (LL5) ordinary chondrite using micro-Raman and infrared spectroscopic technique. The micro-Raman spectrum exhibits the diamond and graphite peaks correspondingly at 1331 cm-1 , 1349 cm-1 and 1588-1618 cm-1. The full wave at half maximum value of about 18 cm-1 for Sadiya indicating the nature of disordered phase involved shock metamorphism in the meteorite samples. The diamond and graphite peaks intensity ratio (~0.53) indica… Show more

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Cited by 4 publications
(3 citation statements)
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References 37 publications
(43 reference statements)
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“…The distinctive peak doublets at 820–822 and 853–854 cm −1 are indicative of Mg‐rich olivine (forsterite) and are mainly due to coupling between the symmetric and asymmetric stretching modes of non‐bridging Si‐O bonds in SiO 4 tetrahedra of olivine (Lam et al, 1990; Pittarello et al, 2015; Saikia et al, 2009). However, the relative height and position of these Raman peaks depend upon the crystal orientation and the compositional ratio of olivine end members (e.g., Chopelas, 1991; Iishi, 1978; Saikia et al, 2016, 2017). The peak at 917.55 cm −1 in olivine indicates polymerization of SiO 4 tetrahedra and closely matches wadsleyite (a high‐pressure polymorph of Mg‐olivine) whose strongest Raman peak appears at 918 cm −1 (Acosta‐Maeda et al, 2013; McMillan & Akaogi, 1987; Ray et al, 2017).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The distinctive peak doublets at 820–822 and 853–854 cm −1 are indicative of Mg‐rich olivine (forsterite) and are mainly due to coupling between the symmetric and asymmetric stretching modes of non‐bridging Si‐O bonds in SiO 4 tetrahedra of olivine (Lam et al, 1990; Pittarello et al, 2015; Saikia et al, 2009). However, the relative height and position of these Raman peaks depend upon the crystal orientation and the compositional ratio of olivine end members (e.g., Chopelas, 1991; Iishi, 1978; Saikia et al, 2016, 2017). The peak at 917.55 cm −1 in olivine indicates polymerization of SiO 4 tetrahedra and closely matches wadsleyite (a high‐pressure polymorph of Mg‐olivine) whose strongest Raman peak appears at 918 cm −1 (Acosta‐Maeda et al, 2013; McMillan & Akaogi, 1987; Ray et al, 2017).…”
Section: Resultsmentioning
confidence: 99%
“…The olivine spectra are dominated by the SiO 4 tetrahedra internal stretching and bending modes (Voropaev et al, 2021). The distinctive peak doublets at 820-822 and 853-854 cm À1 are indicative of Mg-rich olivine (forsterite) and are mainly due to coupling between the symmetric and asymmetric stretching modes of non-bridging Si-O bonds in SiO 4 tetrahedra of olivine (Lam et al, 1990;Pittarello et al, 2015;Saikia et al, 2009). However, the relative height and position of these Raman peaks depend upon the crystal orientation and the compositional ratio of olivine end members (e.g., Chopelas, 1991;Iishi, 1978;Saikia et al, 2016Saikia et al, , 2017.…”
Section: Raman Spectroscopymentioning
confidence: 99%
“…In the FTIR spectrum of ZnO, the broad peak at around 3450 depicts O-H stretching vibrations, that could have been absorbed by the photocatalyst from the solvent (water). A sharp peak at 1620 cm -1 indicates carbonyl acetate group (-COO -), from zinc acetate, stretching frequency (Saikia et al, 2018). The band ranging from 800-500 cm -1 indicates Zn-O stretching vibrations (El-Kemary et al, 2010;Lavand and Malghe, 2016).…”
Section: Ftir Studiesmentioning
confidence: 99%