scholarly journals STRUCTURAL, MORPHOLOGICAL AND VIBRATIONAL STUDIES OF MAGNESIUM DOPED LITHIUM TITANATE ANODE MATERIALS FOR LI-ION BATTERIES

2020 ◽  
Vol 8 (11) ◽  
pp. 386-394
Author(s):  
D. Vijaya Lakshmi ◽  
◽  
B. Vikram Babu ◽  
M. Sushma Reddi ◽  
M. K. Raju ◽  
...  
Keyword(s):  
Thermal Analysis ◽  
Anode Materials ◽  
Lithium Titanate ◽  
Wide Distribution ◽  
X Ray Diffraction ◽  
Spinel Type ◽  
Ft Ir ◽  
Vibrational Studies ◽  
Ir Spectroscopic ◽  
Li4ti5o12 Anode

In the present paper, we study the results of the substitution of Mg2+ in Li4Ti5O12 anode materials with the chemical composition of Li4-xMgxTi5O12 with x = 0, 0.1 and 0.3. Spinel structured Li4-xMgxTi5O12 materials are prepared by conventional ceramic method. The structural, morphological, chemical compostion and vibrational studies of the prepared anode samples are systematically characterized by thermal analysis, XRD, SEM, EDS and FT-IR. Phase formation is confirmed by thermal analysis followed by the XRD and FT-IR spectroscopic results. The X-ray diffraction (XRD) technique exposed that the materials belonged to spinel type having the space group as Fd-3m. Synthesized samples are quite large upto 0.98 to 1.3 ?m in diameter and the grain size had a wide distribution range. EDS is used to identify the elements. The FT-IR spectra show tetrahedral and octahedral sites to be inhabited by the MO6 oxide lattice.

Luminescent Properties of Zn2SiO4:Eu3+,Dy3+ Phosphors via Sol-Gel Process

2012 ◽  
Vol 217-219 ◽  
pp. 733-736
Author(s):  
Xiu Mei Han ◽  
Shu Ai Hao ◽  
Ying Ling Wang ◽  
Gui Fang Sun ◽  
Xi Wei Qi
Keyword(s):  
Thermal Analysis ◽  
Ir Spectra ◽  
Sol Gel ◽  
Luminescent Properties ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sol Gel Process ◽  
Ft Ir

Zn2SiO4:Eu3+, Dy3+ phosphors have been prepared through the sol-gel process. X-ray diffraction (XRD), thermogravimetric and ddifferential thermal analysis (TG-DTA), FT-IR spectra and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicated that the phosphors crystallized completely at 1000oC. In Zn2SiO4:Eu3+,Dy3+ phosphors, the Eu3+ and Dy3+ show their characteristic red(613nm, 5D0-7F2), blue (481nm, 4F9/2–6H15/2) and yellow (577nm, 4F9/2–6H13/2) emissions.

Preparation and Characterization the Cheap Mineral (Calcium Compound): The Preliminary Survey in the Natural Material

2013 ◽  
Vol 770 ◽  
pp. 303-306
Author(s):  
A. Montree ◽  
K. Teanchai ◽  
Wichian Siriprom
Keyword(s):  
Molecular Composition ◽  
Natural Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Conventional Analysis ◽  
Calcium Compound ◽  
Egg Shells ◽  
Ft Ir ◽  
Ir Study ◽  
Ir Spectroscopic

The present work reports the production of biomaterial, while the potential in bio mineralization were studied with three conventional analysis techniques, X-Ray Diffraction (XRD) were confirm the crystal structure, Energy Dispersive X-Ray Fluorescence (EDXRF) and Fourier Transform Infrared Spectroscopy (FT-IR) study trace element and molecular composition, respectively. The results of XRD reveal that, the egg shells have a crystalline of calcium carbonate in phase calcite and fishbone have a crystalline of calcium phosphate in phase hydroxyapatite, respectively. The composition of both mineral and the level of metals element were investigated by EDXRF. The major composition was identified as Calcium (Ca) and other element are Potassium (K), Phosphorus (P) Sulfur (Al), Zinc (Zn), Ferrum (Fe), Copper (Cu) and Strontium (Sr). In addition, the deeply investigate molecular composition both mineral used using FT-IR spectroscopic analysis.

scholarly journals Investigation on optical, electrical and etching properties of 2-aminopyridinium 4-aminobenzoate: A phase matchable organic single crystal for optoelectronic device applications

2017 ◽  
Vol 35 (1) ◽  
pp. 126-134 ◽  
Author(s):  
L. Chandra ◽  
J. Chandrasekaran ◽  
K. Perumal ◽  
B. Babu ◽  
V. Jayaramakrishnan
Keyword(s):  
Optoelectronic Device ◽  
Spectroscopic Studies ◽  
Average Particle ◽  
Dielectric Study ◽  
X Ray Diffraction ◽  
Device Applications ◽  
Evaporation Technique ◽  
Ft Ir ◽  
Ir Spectroscopic ◽  
Homo Lumo

AbstractNLO active 2-aminopyridinium 4-aminobenzoate (APAB) single crystals were successfully grown by the standard slow evaporation technique. The crystallinity of the grown crystals was analyzed through X-ray diffraction (XRD) measurements. Fourier transform infrared (FT-IR) spectroscopic studies were also performed for the identification of different modes present in the compound. The UV-Vis absorption and transmittance spectra were recorded for the grown crystal and the optical band gap was calculated. Birefringence and etching studies were also carried out. The dielectric study showed that the dielectric constant decreased with an increase in frequency. The photoconductivity study revealed its positive photoconducting nature. Theoretical HOMO LUMO investigations were also made for the crystal. The relative SHG efficiency of the material was investigated by the Kurtz and Perry powder technique. The phase matching property of the crystal was studied through the SHG dependence of average particle sizes.

Synthesis, Characterization and Magnetism of Nanosized Copper Ferrite

2008 ◽  
Vol 368-372 ◽  
pp. 604-606 ◽  
Author(s):  
Wei Zhong Lv ◽  
Zhong Kuang Luo ◽  
Bo Liu ◽  
Xiang Zhong Ren ◽  
Hong Hua Cai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Copper Ferrite ◽  
Sonochemical Method ◽  
Thermal Gravimetric ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ft Ir ◽  
Scanning Electron

Copper ferrite powders were successfully synthesized by sonochemical method. The resultant powders were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), FT-IR, differential thermal analysis-thermal gravimetric (DTA-TG), differential scanning calorimetry (DSC) and VSM. The particle saturation magnetization (Ms) is 66 emu/g and an intrinsic coercive force (iHc) is 2100 Oe when the precursor calcined at 950 °C for 15 h.

Comparison of FT-IR, Thermal Analysis and XRD for Determination of Products of Cement Hydration

2010 ◽  
Vol 168-170 ◽  
pp. 518-522 ◽  
Author(s):  
Zhi Hua Ou ◽  
Bao Guo Ma ◽  
Shou Wei Jian
Keyword(s):  
Thermal Analysis ◽  
Fourier Transform ◽  
Cement Hydration ◽  
Hydration Products ◽  
X Ray Diffraction ◽  
Cement Pastes ◽  
X Ray ◽  
Degree Of Hydration ◽  
Ft Ir

Fourier Transform Infrared Spectroscopy (FT-IR), thermal analysis and X-Ray Diffraction (XRD) are commonly performed to study the hydration products in cement pastes. The three methods were compared in this frame to detect products of cement hydration at different ages, especially at early ages (before 24h ages). The results indicate from the present experiment that CH (Calcium hydroxide) can be detected by three methods at all ages; C-S-H can be distinguished by FT-IR at all ages; ettringite may be detected by FT-IR before 24h ages and by XRD at all ages; and monosulphate can be detected by FT-IR before 24h ages. The process of cement hydration, characterized by formation and development of some hydration products, can be clearly observed by three methods. FT-IR is suggested for detecting the major hydration products before 24h ages, FT-IR and XRD are suggested for detecting the major hydration products after 24h ages, and thermal analysis is suggested for analyzing the degree of hydration quantitatively.

Syntheses and crystal structures of new aurate salts of adenine or guanine nucleobases

2020 ◽  
Vol 76 (2) ◽  
pp. 139-147
Author(s):  
Anton Savchenkov ◽  
Ludmila Demina ◽  
Alexey Safonov ◽  
Mikhail Grigoriev ◽  
Roman Solovov ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Noncovalent Interactions ◽  
Spectroscopic Techniques ◽  
Stacking Interactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Nitrogenous Base ◽  
Ir Spectroscopic ◽  
Chloride Monohydrate

Two new gold(III) complexes with adenine or guanine nitrogenous bases as counter-cations were synthesized. These are 6-amino-7H-purine-1,9-diium tetrachloridogold(III) chloride monohydrate, (C5H7N5)[AuCl4]Cl·H2O, 1, and 2-amino-6-oxo-6,7-dihydro-1H-purin-9-ium tetrachloridogold(III) hemihydrate, (C5H6N5O)[AuCl4]·0.5H2O, 2. Their crystal structures were studied using single-crystal X-ray diffraction and FT–IR spectroscopic techniques. The arrangement of species in the studied crystal structures implies π-stacking interactions, as well as concomitant C—H...π interactions, hydrogen bonds and other types of noncovalent interactions, which were studied qualitatively and quantitatively using the method of molecular Voronoi–Dirichlet polyhedra. The variation of the nitrogenous base from adenine to guanine results in evident differences in the packing of the species in the crystals of 1 and 2. The splitting and shifting of bands in the FT–IR spectra of the title compounds reveals several features representative of noncovalent interactions in their crystal structures.

Synthesis, crystal structures and characterizations of three new copper(II) complexes including anti-inflammatory diclofenac

2019 ◽  
Vol 75 (4) ◽  
pp. 388-397 ◽  
Author(s):  
Sevim Hamamci Alisir ◽  
Necmi Dege ◽  
Recep Tapramaz
Keyword(s):  
Thermal Analysis ◽  
Ir Spectroscopy ◽  
Magnetic Data ◽  
X Ray Diffraction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Ft Ir ◽  
Fourier Transform Ir ◽  
Electron Paramagnetic ◽  
Ft Ir Spectroscopy

Three new diclofenac-based copper(II) complexes, namely tetrakis{μ-2-[2-(2,6-dichloroanilino)phenyl]acetato-κ2 O:O′}bis(methanol-κO)copper(II), [Cu2(μ-dicl)4(CH3OH)2] (1), bis{2-[2-(2,6-dichloroanilino)phenyl]acetato-κ2 O,O′}bis(1-vinyl-1H-imidazole-κN 3)copper(II), [Cu(dicl)2(vim)2] (2), and bis{2-[2-(2,6-dichloroanilino)phenyl]acetato-κ2 O,O′}bis(1H-imidazole-κN 3)copper(II), [Cu(dicl)2(im)2] (3) [dicl is diclofenac (C14H10Cl2NO2), vim is 1-vinylimidazole (C5H6N2) and im is imidazole (C3H4N2)], have been synthesized and characterized by elemental analysis, FT–IR spectroscopy, thermal analysis and single-crystal X-ray diffraction. X-ray diffraction analysis shows that complex 1 consists of dimeric units in which the dicl ligand exhibits a bidentate syn,syn-μ2 coordination mode linking two copper(II) centres. Complexes 2 and 3 have mononuclear units with the general formula [Cu(dicl)2 L 2] (L is vim or im) in which the CuII ions are octahedrally coordinated by two L and two dicl chelating ligands. The L and dicl ligands both occupy the trans positions of the coordination octahedron. The different coordination modes of dicl in the title complexes were revealed by Fourier transform IR (FT–IR) spectroscopy. The spin matching between the copper(II) centres in the dimeric [Cu2(μ-dicl)4(CH3OH)2] units was also confirmed by magnetic data to be lower than the spin-only value and electron paramagnetic resonance (EPR) spectra. The thermal properties of the complexes were investigated by thermogravimetric (TG) and differential thermal analysis (DTA) techniques.

Preparation and Analysis of Kaolinite Intercalated by Potassium Acetate

2010 ◽  
Vol 150-151 ◽  
pp. 1220-1224
Author(s):  
Xiao Man Du ◽  
Qin Fu Liu ◽  
Hong Fei Cheng
Keyword(s):  
Thermal Analysis ◽  
Electron Microscope ◽  
Fourier Transformation ◽  
Potassium Acetate ◽  
Basal Spacing ◽  
X Ray Diffraction ◽  
Immersion Method ◽  
X Ray ◽  
Ft Ir ◽  
Scanning Electron

The kaolinite-potassium acetate composite was prepared by the immersion method. The intercalation composites were characterized by means of Scanning Electron Microscope (SEM), X-ray diffraction (XRD), Fourier transformation infrared (FT-IR) and High-resolution thermogravimetric analysis (HRTG). The results of XRD show that the intercalation of kaolinite by potassium acetate causes an increase of the basal spacing from 0.718 to 1.42nm. Thermal analysis shows the dehydroxylation of kaolinite decreased from 464 °C to 459.5 °C after intercalation of potassium acetate and three endotherms at 280, 323 and 459.5 °C attributed to the loss of water in the composite, potassium acetate and hydroxyl in the composite.

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