scholarly journals Welcome to Raman Spectroscopy: Successes, Challenges, and Pitfalls

Elements ◽  
2020 ◽  
Vol 16 (2) ◽  
pp. 87-92 ◽  
Author(s):  
Jill D. Pasteris ◽  
Olivier Beyssac

Geoscientists quickly recognized the broad applicability of Raman micro-probe spectroscopy to the Earth and planetary sciences, especially after commercially built microprobe instruments became available in the early 1980s. Raman spectra are sensitive to even minor (chemical or structural) perturbations within chemical bonds in (even amorphous) solids, liquids, and gases and can, thus, help identify, characterize, and differentiate between individual minerals, fluid inclusions, glasses, carbonaceous materials, solid solution phases, strain in minerals, and dissolved species in multi-component solutions. The articles in this issue explore how Raman spectroscopy has deepened and broadened our understanding of geological and extraterrestrial materials and processes.

2009 ◽  
Vol 2009 ◽  
pp. 1-4 ◽  
Author(s):  
L. Bourja ◽  
B. Bakiz ◽  
A. Benlhachemi ◽  
M. Ezahri ◽  
J. C. Valmalette ◽  
...  

A series of ceramics samples belonging to theCeO2-Bi2O3phase system have been prepared via a coprecipitation route. The crystallized phases were obtained by heating the solid precursors at600∘Cfor 6 hours, then quenching the samples. X-ray diffraction analyses show that forx<0.20a solid solutionCe1−xBixO2−x/2with fluorine structure is formed. For x ranging between 0.25 and 0.7, a tetragonalβ′phase coexisting with the FCC solid solution is observed. For x ranging between 0.8 and 0.9, a new tetragonalβphase appears. Theβ′phase is postulated to be a superstructure of theβphase. Finally, close tox=1, the classical monoclinicα Bi2O3structure is observed. Raman spectroscopy confirms the existence of the phase changes as x varies between 0 and 1.


Author(s):  
E. López-Honorato ◽  
P. J. Meadows ◽  
J. Tan ◽  
Y. Xiang ◽  
P. Xiao

In this work we have deposited silicon carbide (SiC) at 1300°C with the addition of small amounts of propylene. The use of propylene and high concentrations of methyltrichlorosilane (9 vol %) allowed the deposition of superhard SiC coatings (42 GPa). The superhard SiC could result from the presence of a SiC–C solid solution, undetectable by X-ray diffraction but visible by Raman spectroscopy. Another sample obtained by the use of 50 vol % Argon, also showed the formation of SiC with good properties. The use of a flat substrate together with the particles showed the importance of carrying out the analysis on actual particles rather than in flat substrates. We show that it is possible to characterize the anisotropy of pyrolytic carbon by Raman spectroscopy.


2018 ◽  
Vol 56 (1A) ◽  
pp. 197
Author(s):  
Nguyen Hoang Tuan

In this study, we present some results on the structure and properties of the solid solution of Bi0.5K0.5TiO3– BiFeCoO3 (BKT – BFCO) by Sol-gel method. Crystal structures of BKT – BFCO solid solutions were studies by XRD and Raman spectroscopy. The results were in good agreement with the previous reports of Bi0.5K0.5TiO3– BiFeO3 (BKT – BFO) and Bi0.5K0.5TiO3 – BiCoO3 (BKT – BCO) solid solutions. The magnetic properties were investigated via unsaturated M-H loop, which showed the competition of paramagnetic and antiferromagnetic ordering in BKT – BFCO. However, differing from the BKT – BFO and BKT – BCO solid solutions, the unclear values of saturated magnetism in BKT – BFCO raised the unexplained question, which needed further studies.


Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 878 ◽  
Author(s):  
Abdallah Zedan ◽  
Amina AlJaber

In this study, xCuO-CeO2 mixed oxide catalysts (Cu weight ratio x = 1.5, 3, 4.5, 6 and 15 wt.%) were prepared using solution combustion synthesis (SCS) and their catalytic activities towards the methane (CH4) oxidation reaction were studied. The combustion synthesis of the pure CeO2 and the CuO-CeO2 solid solution catalysts was performed using copper and/or cerium nitrate salt as an oxidizer and citric acid as a fuel. A variety of standard techniques, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), thermo-gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were employed to reveal the microstructural, crystal, thermal and electronic properties that may affect the performance of CH4 oxidation. The CuO subphase was detected in the prepared solid solution and confirmed with XRD and Raman spectroscopy, as indicated by the XRD peaks at diffraction angles of 35.3° and 38.5° and the Ag Raman mode at 289 cm−1, which are characteristics of tenorite CuO. A profound influence of Cu content was evident, not only affecting the structural and electronic properties of the catalysts, but also the performance of catalysts in the CH4 oxidation. The presence of Cu in the CeO2 lattice obviously promoted its catalytic activity for CH4 catalytic oxidation. Among the prepared catalysts, the 6% CuO-CeO2 catalyst demonstrated the highest performance, with T50 = 502 °C and T80 = 556 °C, an activity that is associated with the availability of a fine porous structure and the enhanced surface area of this catalyst. The results demonstrate that nanocrystalline copper-ceria mixed oxide catalysts could serve as an inexpensive and active material for CH4 combustion.


2019 ◽  
Vol 481 (1) ◽  
pp. 211-230 ◽  
Author(s):  
Dinesh S. Chauhan ◽  
Rajesh Sharma ◽  
D. R. Rao

AbstractThe present study reports and investigates ‘lazulite’ occurring in the vicinity of a highly tectonized zone of the Main Central Thrust (MCT) in the Himalaya. The azure blue lazulite, hosted in quartz veins, occurs in fractured Berinag quartzite, which forms the footwall of the MCT near Sobla village in NE Kumaun Himalaya, India. Lazulite was investigated using SEM-EDX, micro Raman spectroscopy, fluid inclusion microthermometry and electron probe microanalysis (EPMA). Lazulite contains inclusions of rutile and hematite and has Mg/(Mg+Fe) ratios of 0.86 to 0.90. The phosphorus in lazulite shows a negative trend with Mg+Al contents. This lazulite is an intermediate solid solution near the lazulite end-member with a cationic composition in the structural formula: Mg0.81–0.89Fe0.10–0.13 Al1.88–1.98P2.00–2.07. Its composition in the lazulite–scorzalite stability field points to a higher temperature of its formation. Fluids trapped as inclusions in lazulite and the associated quartz are generally C–O–H fluid. The fluid inclusion isochors for lazulite, together with the temperature calculated for metamorphism of the equivalent structural level in the adjacent area suggest 500–600°C and 7.25 to 9.25 kbar, which match the peak metamorphic temperature–pressure derived elsewhere for the Higher Himalayan Crystallines. Moderately enriched δD‰ values and H2O–CO2–low NaCl fluid suggest that water from a deep reservoir, more likely a metamorphic fluid, participated in lazulite formation. Classic sigmoidal fluid inclusions in lazulite reveal their development during MCT shearing, whereas the overpressured fluid inclusions suggest a post-lazulite uplift. The MCT lazulite is interpreted to have formed during Himalayan shearing and concurrent metamorphism. The present study also implies that this refractory mineral can sustain fluid inclusions within it against intense deformation conditions, such as in the MCT.


Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1124
Author(s):  
Galina Palyanova ◽  
Evgeny Sidorov ◽  
Andrey Borovikov ◽  
Yurii Seryotkin

The copper-containing agates of the Avacha Bay (Eastern Kamchatka, Russia) have been investigated in this study. Optical microscopy, scanning electron microscopy, electron microprobe analysis, X-ray powder diffraction, Raman spectroscopy, and fluid inclusions were used to investigate the samples. It was found that copper mineralization in agates is represented by native copper, copper sulphides (chalcocite, djurleite, digenite, anilite, yarrowite, rarely chalcopyrite) and cuprite. In addition to copper minerals, sphalerite and native silver were also found in the agates. Native copper is localized in a siliceous matrix in the form of inclusions usually less than 100 microns in size—rarely up to 1 mm—forming dendrites and crystals of a cubic system. Copper sulphides are found in the interstices of chalcedony often cementing the marginal parts of spherule aggregates of silica. In addition, they fill the micro veins, which occupy a cross-cutting position with respect to the concentric bands of chalcedony. The idiomorphic appearance of native copper crystals and clear boundaries with the silica matrix suggest their simultaneous crystallization. Copper sulphides, cuprite, and barite micro veins indicate a later deposition. Raman spectroscopy and X-ray powder diffraction results demonstrated that the Avacha Bay agates contained cristobalite in addition to quartz and moganite. The fluid inclusions study shows that the crystalline quartz in the center of the nodule in agates was formed with the participation of solutions containing a very low salt concentration (<0.3 wt.% NaCl equivalent) at the temperature range 110–50 °C and below. The main salt components were CaCl2 and NaCl, with a probable admixture of MgCl2. The copper mineralization in the agates of the Avacha Bay established in the volcanic strata can serve as a direct sign of their metallogenic specialization.


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