scholarly journals The Fourier transform infrared spectroscopy (FTIR) analysis for the clay mineralogy studies in a clastic reservoir

Author(s):  
Golnaz Jozanikohan ◽  
Mohsen Nosrati Abarghooei

AbstractThe complete characteristics knowledge of clay minerals is necessary in the evaluation studies of hydrocarbon reservoirs. Ten samples taken from two wells in a heterogeneous clastic gas reservoir formation in NE Iran were selected to conduct the transmission Fourier transform infrared spectroscopy (FTIR) tests for the clay mineralogy studies. The FTIR analysis showed that there were clear signs of clay minerals in all samples. The wavenumber region of the clay minerals in FTIR tests was detected to be 3621, 3432, 1034, and 515 cm−1 for illite, 3567, 3432, 1613, 1088, 990, 687, 651, and 515 cm−1 for magnesium-rich chlorite, 3700, 3621, 3432, 1034, 687, and 463 cm−1 for kaolinite, and 3567, 1088, 990, and 463 cm−1 for glauconite. After screening of samples by the FTIR method, the samples were then analyzed by powder X-ray diffraction (PXRD), wavelength dispersive X-ray fluorescence (WDXRF), and scanning electron microscopy (SEM). The PXRD and SEM result showed illite was by far the most common clay present. Kaolinite, magnesium-rich chlorite, and traces of smectite and the mixed-layer clays of both the illite–smectite and chlorite-smectite types were also recognized. The combination of PXRD and WDXRF results could quantify the clay abundances in the each well too. It was concluded that the FTIR analysis successfully could show the absorption bonds of all constituent clays. However, the infrared absorption spectra of mixed-layer clays overlapped those of the respective constituents of each mixed-layer minerals. This can be considered as the evidence of the usefulness of FTIR technique in the screening of the samples for the clay mineralogy studies.

2019 ◽  
Vol 70 (8) ◽  
pp. 2747-2752
Author(s):  
Constantin Marutoiu ◽  
Ioan Bratu ◽  
Mircea Gelu Buta ◽  
Olivia Florena Nemes ◽  
Sergiu Petru Timbus(Monk Siluan) ◽  
...  

A two-sided wooden icon from a monastery in Transylvania was submitted for multidisciplinary investigations involving X-Ray Fluorescence, Radiographic Photographyand Fourier Transform Infrared Spectroscopy. The most important part of the icon is St. Nicholas wooden icon, painted over forty years ago. The spectroscopic methods used revealed the painting materials composition, the status of the wooden stage, and the presence of resins as varnish (Fourier Transform Infrared Spectroscopy). On one side, the St Nicholasicon was painted over an old icon, St. Arch. Michael, which was evidenced by X-Ray Photography. The obtained data can serve for the preservation and the restoration of these wooden icons.


2021 ◽  
pp. 152808372110592
Author(s):  
Vahid Shakeri Siavashani ◽  
Gursoy Nevin ◽  
Majid Montazer ◽  
Pelin Altay

Flexible sensors and wearable electronics have become important in recent years. A good conductive and flexible textile is needed to develop a commercial wearable device. Conductive polymers have generally been used with limitation in reducing the surface resistance to a certain amount. In this research, a method for fabricating a stretchable highly conductive cotton/lycra knitted fabric is introduced by treating the fabric with polypyrrole (PPy), silver nanoparticles (SNPs) composites, and post-treating with poly (3,4-ethylenedioxythiophene) poly (styrenesulfonate) (PEDOT:PSS). Polypyrrole and SNPs were in situ fabricated on the cotton/lycra fabric by consecutive redox reaction of silver nitrate and pyrrole and finally covered by PEDOT:PSS solution through dip-coating. The coated textile was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), X-ray mapping, and energy dispersive X-ray spectroscopy (EDX). Fourier transform infrared spectroscopy confirmed PPy-SNPs (P-S) composites on the fabric surface. Fourier transform infrared spectroscopy results, X-ray mapping, EDAX, and XRD analysis also confirmed the P-S composites and PEDOT:PSS polymeric layer on the fabric. Morphological observation showed a layer of PEDOT:PSS on the P-S caused the higher connection of coating on textiles which resulted in the higher electrical conductivity (43 s/m). Also morphological observations showed penetration of the silver particles inside fibers which represented improving in attachment and stability of the coating on the fibers. Further, the electrical conductivity of PPy-SNPs-PEDOT:PSS coated textile increased under the tension. Hence, the stretchable and highly conductive knitted cotton/lycra fabric has potentiality to be used for fabricating the flexible sensors or wearable electronics.


Author(s):  
S. J. Pradeeba ◽  
K. Sampath

This research was carried out based on the significance of protecting the environment by preventing the contamination of water caused from effluents discharge from dyeing industries, effective nanocomposite were prepared to solve this problem. The poly(azomethine), ZnO, and poly(azomethine)/ZnO nanocomposites were prepared and characterized by Fourier transform-infrared spectroscopy, ultraviolet (UV)–visible spectroscopy, powder X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDAX), scanning electron Microscope (SEM), and transmission electron microscopy (TEM) techniques. Methylene blue (MB), Malachite green (MG), and Bismarck brown (BB) were degraded from water using poly(azomethine) (PAZ), zinc oxide (ZnO), PAZ/ZnO (PNZ) nanocomposites as photocatalyst in the presence of natural sunlight. The degradation efficiency and reaction kinetics were calculated, and the outcome of the photocatalytic experiments proved that the PAZ/ZnO nanocomposites reveals excellent photocatalytic activity and effective for decolorization of dye containing waste water than PAZ and ZnO in the presence of natural sunlight. The maximum degradation efficiency 97%, 96%, and 95% was obtained for PNZ nanocomposites at optimum dosage of catalyst as 500 mg and 50 ppm of MB, MG, and BB dye concentration, respectively. The maximum degradation time was 5 h. After photocatalytic study, the samples were characterized by Fourier-transform infrared spectroscopy (FT-IR) and UV–visible spectroscopy.


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