A Raman spectroscopic study of the natural carbonophosphates Na3MCO3PO4 (M = Mn, Fe, and Mg)

Author(s):  
Ekaterina Fomina ◽  
Evgeniy Kozlov ◽  
Mikhail Sidorov ◽  
Vladimir Bocharov

<p>Along with some other Na-minerals, carbonophosphates indicate a high initial Na activity in carbonatite and kimberlite melts, which is beneficial for petrological reconstructions. Because carbonophosphates are capable of incorporating large-ion lithophile and rare earth elements (REEs) in their structure, they can participate in the transport of these elements. Moreover, due to the presence of both [PO<sub>4</sub>]<sup>3−</sup> and [CO<sub>3</sub>]<sup>2− </sup>groups in carbonophosphates, these mineral phases play an important role in the Earth's global carbon and phosphate cycles. With all these properties, carbonophosphates have long attracted the attention of geologists. Raman spectroscopy appears to be one of the most suitable tools for their diagnosis, since they commonly present in rocks as small inclusions in other mineral grains. Despite this profit, only a few publications contain Raman characteristics of either natural or synthetic carbonophosphates.</p><p>We studied and compared Raman spectra of three natural carbonophosphate phases (sidorenkite, bonshtedtite, and bradleyite) with the general formula Na<sub>3</sub>MCO<sub>3</sub>PO<sub>4</sub> (M = Mn, Fe, and Mg, correspondingly). These spectra showed from 21 to 24 vibrational bands, of which the two most intense (963±5 cm<sup>-1</sup> и 1074±3 cm<sup>-1</sup>) correspond to the ν1(P–O) and ν1(C–O) modes. These two bands split due to the occurrence of isomorphic impurities. It was found that the crystallographic orientation of the sample influences the intensity of most bands. A natural increase in the Raman shift was observed for most bands assigned to the same vibrations (the smallest shift in the spectrum is characteristic of sidorenkite, an intermediate - of bonshtedtite, and the largest - of bradleyite).</p><p>We propose the following algorithm for the diagnosis of carbonophosphates:</p><ul><li>Checking minerals for belonging to the group of carbonophosphates by the main bands and the characteristic profile of the spectrum;</li> <li>Testing the hypothesis that the mineral of question is bradleyite based on the analysis of the estimated shift of the main bands;</li> <li>Diagnosis of a mineral species by peaks located between the main bands;</li> <li>Validation of the diagnostics by considering the position of the bands at 185±9 cm<sup>-1</sup>, 208±7 cm<sup>-1</sup>, 255±5 cm<sup>-1</sup>, and 725±6 cm<sup>-1</sup>.</li> </ul><p>The proposed algorithm allows one to perform Raman diagnostics of carbonophosphates in inclusions even in the absence of EPMA data. In the study of carbonatites, kimberlites, and other rocks, the diagnostics of the mineral species of the carbonophosphate group can be important in the petrological aspect.</p><p>This research was funded by the Russian Science Foundation, grant number 19-77-10039.</p>

2021 ◽  
Vol 33 (3) ◽  
pp. 283-297
Author(s):  
Evgeniy Nikolaevich Kozlov ◽  
Ekaterina Nikolaevna Fomina ◽  
Vladimir Nikolaevich Bocharov ◽  
Mikhail Yurievich Sidorov ◽  
Natalia Sergeevna Vlasenko ◽  
...  

Abstract. Raman spectra of three natural carbonophosphates (sidorenkite, bonshtedtite, and bradleyite) with the general formula Na3MCO3PO4 (M is Mn, Fe, and Mg) were studied and compared. These spectra showed from 21 to 24 vibrational bands, of which the two most intense (964±5 and 1074±3 cm−1) correspond to the υ1(P–O) and υ1(C–O) modes. These two bands split into doublet peaks due to the occurrence of isomorphic impurities. It was found that the crystallographic orientation of the sample influences the intensity of most bands. Most bands assigned to the same vibrations showed a regular shift (the smallest in sidorenkite spectra, an intermediate in bonshtedtite, and the largest in bradleyite). We propose an algorithm that allows for diagnostics of carbonophosphates in inclusions by their Raman spectra, providing a reliable result even in the absence of energy-dispersive X-ray spectroscopy (EDX) data.


1987 ◽  
Vol 65 (3) ◽  
pp. 491-496 ◽  
Author(s):  
Serge Alex ◽  
Rodrigue Savoie

A systematic Raman spectroscopic investigation of the complexation of CH3Hg+ by the standard amino acids is reported. It is shown that the vibrational bands due to the ligand—Hg and Hg—CH3 stretching modes and to the symmetric —CH3 bending mode of the —HgCH3 unit are well suited to characterize the extent of complexation and the sites of attachment of the cation. Coordination, which occurs mostly on sulfur and nitrogen atoms by substitution of a proton on the thiol group of cysteine or on amino groups in general, is best identified by the frequency of the ligand—Hg stretching vibration in the 250–550 cm−1 region of the spectrum.


2021 ◽  
Author(s):  
Muhammad Azeem

Abstract Raman spectra are collated from the cement paste matrices of CNTs, ZnO, Gd2O3, and SiO2. The spectra show that CNTs do not take part in hydration process and therefore concentration of calcium silicate hydrate (CSH) is unchanged in CNT-OPC matrix. The metal oxides, on the other hand, have shown significant effects on the CSH concentration. The CSH concentration increases with the increase of ZnO weight percent in the matrix whereas spectra collected from Gd2O3 matrix shows the strongest CSH vibrational bands. Moreover, vibrational bands of CaCO3 also become weak in the matrices with Gd2O3. The addition of SiO2 however had opposite effects that is by increasing the weight percent of SiO2 in the matrix, the CSH concentration is decreased. Since CSH acts a glue in a binder, the study shows that its concentration can be controlled by adding foreign elements. Such binders are expected to show improved strength and durability.


2021 ◽  
Vol 118 (13) ◽  
pp. 133101
Author(s):  
Sanghyun Kim ◽  
Donghyeon Lee ◽  
Binbin Wang ◽  
Shang-Jie Yu ◽  
Kenji Watanabe ◽  
...  

2021 ◽  
Vol 22 (10) ◽  
pp. 5380
Author(s):  
Boris A. Kolesov

The work outlines general ideas on how the frequency and the intensity of proton vibrations of X–H×××Y hydrogen bonding are formed as the bond evolves from weak to maximally strong bonding. For this purpose, the Raman spectra of different chemical compounds with moderate, strong, and extremely strong hydrogen bonds were obtained in the temperature region of 5 K–300 K. The dependence of the proton vibrational frequency is schematically presented as a function of the rigidity of O-H×××O bonding. The problems of proton dynamics on tautomeric O–H···O bonds are considered. A brief description of the N–H···O and C–H···Y hydrogen bonds is given.


1978 ◽  
Vol 9 (40) ◽  
Author(s):  
J. MEDEMA ◽  
C. VAN STAM ◽  
V. H. J. DE BEER ◽  
A. J. A. KONINGS ◽  
D. C. KONINGSBERGER

Heritage ◽  
2021 ◽  
Vol 4 (1) ◽  
pp. 524-540
Author(s):  
Philippe Colomban ◽  
Gulsu Simsek Franci ◽  
Farahnaz Koleini

In the late 19th century, ancient tombs were discovered near the village of Vohemar at the northeastern point of Madagascar, and subsequent excavations during the French period (1896–1945) revealed the presence of a major necropolis active from ~13th to 18th centuries. Some artefacts (Chinese ceramic shards and glass trade beads) recovered from these excavations was sent to France and now in part belong to the collection of the Musée d’Histoire Naturelle, Nimes. Carnelian and glass trade beads were analyzed with a mobile Raman spectrometer, which identified different materials (soda-lime glass, quartz/moganite, carnelian/citrine, chalcedony) and coloring agents (Naples yellow, cassiterite, amber chromophore, transition metal ions, etc.). The results are compared with those obtained on beads excavated at different sites of Southern Africa and at Mayotte Island, and it appears that (most of) the beads come from southern Asia and Europe. The results confirmed the role that northern Madagascar played within the maritime networks of the Western Indian Ocean during the 15th–16th century.


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