The Hydrothermal Synthesis of KzMnO2 in the Presence of Citric Acid

1998 ◽  
Vol 548 ◽  
Author(s):  
Pramod K. Sharma ◽  
Gregory J. Moore ◽  
M. Stanley Whittingham
Keyword(s):  
Citric Acid ◽  
Hydrothermal Synthesis ◽  
Chemical Analysis ◽  
Cathode Material ◽  
Layered Structure ◽  
X Ray Diffraction ◽  
Hydrothermal Preparation ◽  
X Ray ◽  
Impedance Data ◽  
Li Batteries

ABSTRACTKxMnO2 exhibits a layered structure that provides attractive properties as a cathode material for secondary Li batteries. Therefore, in the present study, our attention was paid to the hydrothermal preparation of highly homogenous KxMnO2 in presence of citric acid. Out X-ray diffraction and SEM studies indicated that the final product markedly change the phase and morphology on vary the concentration of citric acid. The prepared products have also studied with the help of TGA and DTA. EDS and DCP made the chemical analysis of the compounds. The impedance data of the materials were explained in terms of the compounds formed.

Hydrothermal Preparation of B-Doped TiO2 and Photodegradation of Salicylic Acid under Visible Light

2012 ◽  
Vol 557-559 ◽  
pp. 1592-1595 ◽  
Author(s):  
Xiao Lin Liu ◽  
Wen Lu Guo ◽  
Jing Jing Ma
Keyword(s):  
Salicylic Acid ◽  
Electron Microscope ◽  
Hydrothermal Synthesis ◽  
Visible Light ◽  
Degradation Rate ◽  
Diffuse Reflectance ◽  
X Ray Diffraction ◽  
Hydrothermal Preparation ◽  
X Ray ◽  
Scanning Electron

B-doped TiO2 nanoparticles have been successfully prepared using hydrothermal synthesis with tetrabuttyl titanate and boric acid as precursor. The prepared samples were characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectra (UV-vis DRS), scanning electron microscope (SEM). The B-doped TiO2 nanoparticles were red-shifted than P25. And the degradation rate of B-TiO2 is 72.62% in 120 min by degradation of salicylic acid under visible light irradiation.

scholarly journals Физический механизм работы палладий-бариевых катодов СВЧ-приборов

2019 ◽  
Vol 89 (5) ◽  
pp. 771
Author(s):  
В.И. Капустин ◽  
И.П. Ли ◽  
А.В. Шуманов ◽  
С.О. Москаленко ◽  
А.А. Буш ◽  
...  
Keyword(s):  
Phase Composition ◽  
Chemical Analysis ◽  
Cathode Material ◽  
Electron Spectroscopy ◽  
Oxygen Vacancies ◽  
Diffraction Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Chemical States ◽  
Electron Energy Loss

AbstractHigh-resolution X-ray diffraction method (XRD) is used to determine sizes and crystallographic orientation of the nanocrystallites of the Pd and Pd_5Ba phases in palladium–barium cathode. Electron spectroscopy for chemical analysis (ESCA) is used to study Ba and Pd chemical states in cathode material and determine the phase composition including dissolved microimpurities in the phases. The comparison of the XRD and ESCA data makes it possible to reveal effects related to the formation of the BaO crystallites in the cathode material, which are responsible for the emission properties. Electron-energy loss spectroscopy is used to determine the concentration of oxygen vacancies in the BaO crystallites that are formed in the cathode material due to activation. An original crystallite model of the working palladium–barium cathodes that is based on the results of this work may serve as an alternative to the known film model and makes it possible to optimize technology of cathode fabrication and activation.

Microdomains in BaFeO3-y (0.35 < y < 0.50)

1990 ◽  
Vol 48 (4) ◽  
pp. 780-781
Author(s):  
M. Vallet-Regí ◽  
M. Parras ◽  
J.M. González-Calbet ◽  
J.C. Grenier
Keyword(s):  
Electron Diffraction ◽  
Chemical Analysis ◽  
Monoclinic Phase ◽  
Orthorhombic Phase ◽  
Total Iron ◽  
Zone Axis ◽  
Electron Micrograph ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Variations

BaFeO3-y compositions (0.35<y<0.50) have been investigated by means of electron diffraction and microscopy to resolve contradictory results from powder X-ray diffraction data.The samples were obtained by annealing BaFeO2.56 for 48 h. in the temperature range from 980°C to 1050°C . Total iron and barium in the samples were determined using chemical analysis and gravimetric methods, respectively.In the BaFeO3-y system, according to the electron diffraction and microscopy results, the nonstoichiometry is accommodated in different ways as a function of the composition (y):In the domain between BaFeO2.5+δBaFeO2.54, compositional variations are accommodated through the formation of microdomains. Fig. la shows the ED pattern of the BaFeO2.52 material along thezone axis. The corresponding electron micrograph is seen in Fig. 1b. Several domains corresponding to the monoclinic BaFeO2.50 phase, intergrow with domains of the orthorhombic phase. According to that, the ED pattern of Fig. 1a, can be interpreted as formed by the superposition of three types of diffraction maxima : Very strong spots corresponding to a cubic perovskite, a set of maxima due to the superposition of three domains of the monoclinic phase along [100]m and a series of maxima corresponding to three domains corresponding to the orthorhombic phase along the [100]o.

New Coordination Compounds of Fe(III) with Organic Ligands

2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Mihaela Flondor ◽  
Ioan Rosca ◽  
Doina Sibiescu ◽  
Mihaela-Aurelia Vizitiu ◽  
Daniel-Mircea Sutiman ◽  
...  
Keyword(s):  
Chemical Analysis ◽  
Complex Compounds ◽  
Organic Ligands ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Chemical Analysis ◽  
Structural Formulae ◽  
Paramagnetic Properties

In this paper the synthesis and the study of some complex compounds of Fe(III) with ligands derived from: 2-(4-chloro-phenylsulfanyl)-1-(2-hydroxy-3,5-diiodo-phenyl)-ethanone (HL1), 1-(3,5-dibromo-2-hydroxy-phenyl)-2-phenylsulfanyl-ethanone(HL2), and 2-(4-chloro-phenylsulfanyl)-1-(3,5-dibromo-2-hydroxy-phenyl)-ethanone (HL3) is presented. The characterization of these complexes is based on method as: the elemental chemical analysis, IR and ESR spectroscopy, M�ssbauer, the thermogravimetric analysis and X-ray diffraction. Study of the IR and chemical analysis has evidenced that the precipitates form are a complexes and the combination ratio of M:L is 1:2. The central atoms of Fe(III) presented paramagnetic properties and a octaedric hybridization. Starting from this precipitation reactions, a method for the gravimetric determination of Fe(III) with this organic ligands has been possible. Based on the experimental data on literature indications, the structural formulae of the complex compounds are assigned.

Hydrolytic products of Fe(III) after oxidation of Fe(II) by chlorate

1982 ◽  
Vol 47 (4) ◽  
pp. 1069-1077 ◽  
Author(s):  
Karel Mádlo ◽  
František Hanousek ◽  
Antonín Petřina ◽  
Jaroslav Tláskal
Keyword(s):  
Electron Microscopy ◽  
Ir Spectroscopy ◽  
Chemical Analysis ◽  
Ferrous Sulphate ◽  
Reaction Medium ◽  
Potassium Chlorate ◽  
X Ray Diffraction ◽  
X Ray

Ferrous sulphate was oxidized by potassium chlorate in the pH region 2-7 and at temperatures ranging from 298.1 to 323.1 K and various hydrolytic products of Fe(III) were separated and indentified. The separated solid ferric products were analyzed using a combination of the chemical analysis, IR spectroscopy, X-ray diffraction, and electron microscopy. The following substances were found as major components of the products: Fe2O3.n H2O ("ferric gel"), Fe2O3.n H2O with bound SO2-4 ions ("sulphogel"), α-FeO(OH), γ-FeO(OH) and Fe3O4. Their amount depends particularly on the pH temperature of the reaction medium.

scholarly journals Hydrothermal Synthesis, Characterization and Exploration of Photocatalytic Activities of Polyoxometalate: Ni-CoWO4 Nanoparticles

Crystals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 456
Author(s):  
Fahad A. Alharthi ◽  
Hamdah S. Alanazi ◽  
Amjad Abdullah Alsyahi ◽  
Naushad Ahmad
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Structure Morphology ◽  
Photocatalytic Activities ◽  
Ft Ir ◽  
Photocatalytic Reactions ◽  
Cobalt Tungstate

This study demonstrated the hydrothermal synthesis of bimetallic nickel-cobalt tungstate nanostructures, Ni-CoWO4 (NCW-NPs), and their phase structure, morphology, porosity, and optical properties were examined using X-ray Diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Scanning electron microscopy- energy dispersive X-ray spectroscopy (SEM-EDS), high resolution Transmission electron microscopy (HR-TEM), Brunauer-Emmett-Teller (BET) and Raman instruments. It was found that as-calcined NCW-NPs have a monoclinic phase with crystal size ~50–60 nm and is mesoporous. It possessed smooth, spherical, and cubic shape microstructures with defined fringe distance (~0.342 nm). The photocatalytic degradation of methylene blue (MB) and rose bengal (RB) dye in the presence of NCW-NPs was evaluated, and about 49.85% of MB in 150 min and 92.28% of RB in 90 min degraded under visible light. In addition, based on the scavenger’s study, the mechanism for photocatalytic reactions is proposed.

The first proof of protonated anion tetrahedra in the tsumcorite-type compounds

2004 ◽  
Vol 68 (5) ◽  
pp. 757-767 ◽  
Author(s):  
T. Mihajlović ◽  
H. Effenberger
Keyword(s):  
Crystal Structure ◽  
Hydrothermal Synthesis ◽  
Single Crystal ◽  
Diffraction Data ◽  
Title Compound ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Hydrogen Atoms ◽  
Synthetic Compounds ◽  
X Ray

AbstractHydrothermal synthesis produced the new compound SrCo2(AsO4)(AsO3OH)(OH)(H2O). The compound belongs to the tsumcorite group (natural and synthetic compounds with the general formula M(1)M(2)2(XO4)2(H2O,OH)2; M(1)1+,2+,3+ = Na, K, Rb, Ag, NH4, Ca, Pb, Bi, Tl; M(2)2+,3+ = Al, Mn3+, Fe3+, Co, Ni, Cu, Zn; and X5+,6+ = P, As, V, S, Se, Mo). It represents (1) the first Sr member, (2) the until now unknown [7]-coordination for the M(1) position, (3) the first proof of (partially) protonated arsenate groups in this group of compounds, and (4) a new structure variant.The crystal structure of the title compound was determined using single-crystal X-ray diffraction data. The compound is monoclinic, space group P21/a, with a = 9.139(2), b = 12.829(3), c = 7.522(2) Å, β = 114.33(3)°, V = 803.6(3) Å3, Z = 4 [wR2 = 0.065 for 3530 unique reflections]. The hydrogen atoms were located experimentally.

Geochemistry of halloysite-7Å formation from plagioclase in trachyandesite rocks from Limnos Island, Greece

Clay Minerals ◽  
2014 ◽  
Vol 49 (1) ◽  
pp. 75-89 ◽  
Author(s):  
D. Papoulis ◽  
S. Komarneni ◽  
D. Panagiotaras
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Chemical Analysis ◽  
Geochemical Data ◽  
X Ray Diffraction ◽  
Polarizing Microscopy ◽  
X Ray ◽  
Geochemical Evaluation ◽  
Scanning Electron ◽  
Southwest Part

AbstractTrachyandesite rocks, occurring over an area of about 1 km2in the southwest part of Limnos Island, Greece, are altered mainly to halloysite. The samples were collected and analysed by polarizing microscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and chemical analysis. The alteration of plagioclase to halloysite follows seven discrete stages that are described in detail. The geochemical evaluation of the data shows enrichment of the lightREE(LREE) over heavyREE(HREE) as expressed by the (La/Yb)n ratio. TheΣLREErange from 206.44 to 272.30, while the sum ofHREEvaries from 11.01 to 26.26. The (La/Yb)n ratio ranges from 9.72 to 27.64. Fractionation amongLREEexpressed as (La/Sm)n and between middleREE(MREE) andHREEis shown as (Tb/Yb)n ratios. The most altered rocks close to the fault zone have high (Tb/Yb)n ratios and low (La/Sm)n and Eu/Eu* ratios. Although mineralogy and clay mineral textures indicate hydrothermal genesis of halloysite, the geochemical data are not conclusive due to a secondary weathering effect.

scholarly journals SEDIMENTOLOGIA DE LAGUNAS COSTERAS: CIENAGA GRANDE DE SANTA MARTA Y CIENAGA DE PAJARALES

2016 ◽  
Vol 25 ◽  
Author(s):  
Gladys Bernal ◽  
Julliet Betancur
Keyword(s):  
Grain Size ◽  
Organic Matter ◽  
Chemical Analysis ◽  
X Ray Diffraction ◽  
Caribbean Coast ◽  
X Ray ◽  
Deltaic Plain ◽  
Magdalena River

Ciénaga Grande de Santa Marta and Ciénaga de Pajarales are the two main lagoons of the marginal lagunar system at the deltaic floodplain of Magdalena river, Caribbean coast of Colombia. A systematic surficial sampling was carried out in such lagoons and Salamanca coast. A sporadic sampling was done in other places of the deltaic plain. This paper presents results about grain size, mineralogy, organic matter contents, CaCOa contents, X ray diffraction and chemical analysis of salts for sediments. Sedimentologic charts, distribution schemes and provenience notes are presented.

scholarly journals COMPOSITION, STRUCTURE AND TEXTURAL CHARACTERISTICS OF DOMESTIC ACID ACTIVATED BENTONITE

2014 ◽  
Vol 5 (1) ◽  
Author(s):  
Zоrаn Pеtrоvić ◽  
Pеrо Dugić ◽  
Vојislаv Аlеksić ◽  
Sаbinа Bеgić ◽  
Vlаdаn Мićić ◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Low Temperature ◽  
Layered Structure ◽  
Nitrogen Adsorption ◽  
X Ray Diffraction ◽  
Textural Characteristics ◽  
X Ray ◽  
Before And After ◽  
Activated Bentonite ◽  
Composition Structure

Bentonites are aluminosilicate minerals which, due to their porosity, layered structure and composition have a wide application. Structural and textural characteristics of bentonite may be improved by different modification procedures. The aim of this study was to investigate compositional, structural and textural characteristics of domestic bentonite in place Gerzovo, before and after the activation with sulfuric acid. These characteristics were investigated by analytical methods, X-ray diffraction (XRD) and the method of low-temperature nitrogen adsorption (BET). Characteristics of acid-activated bentonite were compared with the characteristics of commercial active clay. The obtained results showed that the activation of bentonite with sulfuric acid leads to a significant improvement in structural and textural characteristics. Using these results it can be assumed that this bentonite will have good adsorption characteristics and can serve as an alternative in comparison with imported commercial aluminosilicate-based adsorbents.

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