Manganese oxide accumulations associated with some soil structural pores .I. Morphology, composition and genesis

Soil Research ◽  
1992 ◽  
Vol 30 (4) ◽  
pp. 409 ◽  
Author(s):  
LA Sullivan ◽  
AJ Koppi
Keyword(s):  
Manganese Oxide ◽  
Analytical Techniques ◽  
Oxide Phase ◽  
Significant Negative Correlation ◽  
X Ray Diffraction ◽  
Microbial Oxidation ◽  
X Ray ◽  
Positive Correlations ◽  
Typic Pellustert ◽  
Iron And Manganese

The morphology and composition of manganese oxide accumulations associated with the structural pores in a black earth (Typic Pellustert) subsoil layer were examined using light microscopy, electron microscopy, X-ray diffraction and electron micro-analytical techniques. Birnessite was identified as the crystalline manganese oxide phase. There were significant positive correlations between cobalt, calcium and manganese and a significant negative correlation between iron and manganese. It was most probable that both microbial oxidation and auto-oxidation of Mn2+ contributed to the formation of the manganese oxide accumulations in this soil.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

scholarly journals Analytical study of Buddha sculptures in Jingyin temple of Taiyuan, China

2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Xiaojian Bai ◽  
Chen Jia ◽  
Zhigen Chen ◽  
Yuxuan Gong ◽  
Huwei Cheng ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Analytical Study ◽  
Energy Dispersive Spectrometry ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Ancient China ◽  
X Ray ◽  
Unique Style ◽  
Scanning Electron

AbstractWith exquisite design and unique style, the painted sculptures of Tutang Buddha and two attendants Buddha in Jingyin Temple are precious cultural heritages of China. The sculpture of Tutang Buddha, which was carved from a mound and painted by ancient craftsmen, was rarely found in ancient China. However, due to natural and human factors, the sculptures were severely damaged. Obviously, they require urgent and appropriate protection and restoration. In this study, samples taken from the sculptures were analysed through multiple analytical techniques, including scanning electron microscopy with energy dispersive spectrometry (SEM–EDS), Raman spectroscopy, X-ray diffraction (XRD), optical microscopy (OM) and granulometry. The analysis results enable us to infer the techniques used by the craftsmen in making the sculptures and provide a reliable evidence for the conservation and future protection of these and similar sculptures.

Characterization of Silver Binding in Cryptomelane by X-ray Absorption Spectroscopy

1998 ◽  
Vol 524 ◽  
Author(s):  
R. Ravikumar ◽  
D. W. Fuerstenau ◽  
G. A. Waychunas
Keyword(s):  
Manganese Oxide ◽  
Silver Ions ◽  
Oxide Phase ◽  
Synthetic Sample ◽  
Temperature Spectrum ◽  
X Ray ◽  
Room Temperature Sample ◽  
X Ray Absorption ◽  
Temperature Sample

ABSTRACTUsing silver K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy, two different samples of silver-containing manganese oxide were analyzed in the fluorescence mode. For the first sample, silver ions from solution were sorbed onto one synthetic manganese oxide phase, namely cryptomelane (KxMn8O16, where l<x<2). The second sample was a silvermanganese oxide from Colorado. From the EXAFS analysis, silver was found to occupy two different sites in the synthetic sample. The natural samples from Colorado also exhibited a very similar coordination distances as the synthetic samples. In the low temperature spectrum of the synthetic sample at 10 K, the Ag-O peak was found to be missing and the amplitude of the Ag- Ag peak was approximately three times larger than the corresponding room temperature sample.

LiMn2-xCuxO4 Spineis - 5 V Cathode Materials

1997 ◽  
Vol 496 ◽  
Author(s):  
Yair Ein-Eli ◽  
W. F. Howard ◽  
Sharon H. Lu ◽  
Sanjeev Mukerjee ◽  
James McBreen ◽  
...  
Keyword(s):  
Copper Ions ◽  
Oxide Phase ◽  
Electrochemical Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Spinel Compounds ◽  
Composition And Structure ◽  
Phase Spinel ◽  
Lithium Copper Oxide ◽  
X Ray Absorption

ABSTRACTA series of electroactive spinel compounds, LiMn2-xCuxO4 (0.1 ≤ x ≤ 0.5) has been studied by crystallographic, spectroscopie and electrochemical methods and by electron-microscopy. These LiMn2-xCuxO4 spinels are nearly identical in structure to cubic LiMn2O4 and successfully undergo reversible Li intercalation. The electrochemical data show slight shifts to higher voltage for the delithiation reaction that normally occurs at 4.1 V in standard Li1−xMn2O4 electrodes (1 ≥ x ≥ 0) corresponding to the oxidation of Mn3+ to Mn4+. The data also show a remarkable reversible electrochemical process at 4.9 V which is attributed to the oxidation of Cu2+ to Cu3+. The inclusion of Cu in the spinel structure enhances the electrochemical stability of these materials upon cycling. The initial capacity of LiMn2-xCuxO4 spinels decreases with increasing x from 130 mAh/g in LiMn2O4 (x=0) to 70 mAh/g in “LiMn1.5Cu0.5O4”(x=0.5). Although the powder X-ray diffraction pattern of “LiMn1.5Cu0.5 O4” shows a single-phase spinel product, neutron diffraction data show a small, but significant quantity of an impurity phase, the composition and structure of which could not be identified. X-ray absorption spectroscopy was used to gather information about the oxidation states of the manganese and copper ions. The composition of the spinel component in the LiMn1.5Cu0.5O4 was determined from X-ray diffraction and XANES data to be Li1.01Mn1.67Cu0.32O4 suggesting, to a best approximation, that the impurity in the sample was a lithium-copper-oxide phase.

scholarly journals Assay and physicochemical characterization of the antiparasitic albendazole

2012 ◽  
Vol 48 (2) ◽  
pp. 281-290 ◽  
Author(s):  
Noely Camila Tavares Cavalcanti ◽  
Giovana Damasceno Sousa ◽  
Maria Alice Maciel Tabosa ◽  
José Lamartine Soares Sobrinho ◽  
Leila Bastos Leal ◽  
...  
Keyword(s):  
Physicochemical Characterization ◽  
Analytical Techniques ◽  
Assay Method ◽  
Active Pharmaceutical Ingredients ◽  
X Ray Diffraction ◽  
Melting Points ◽  
X Ray ◽  
Pharmaceutical Ingredients ◽  
Complementary Techniques

The aim of this study was to characterize three batches of albendazole by pharmacopeial and complementary analytical techniques in order to establish more detailed specifications for the development of pharmaceutical forms. The ABZ01, ABZ02, and ABZ03 batches had melting points of 208 ºC, 208 ºC, and 209 ºC, respectively. X-ray diffraction revealed that all three batches showed crystalline behavior and the absence of polymorphism. Scanning electron microscopy showed that all the samples were crystals of different sizes with a strong tendency to aggregate. The samples were insoluble in water (5.07, 4.27, and 4.52 mg mL-1, respectively) and very slightly soluble in 0.1 M HCl (55.10, 56.90, and 61.70 mg mL-1, respectively) and additionally showed purities within the range specified by the Brazilian Pharmacopoeia 5th edition (F. Bras. V; 98% to 102%). The pharmacopeial assay method was not reproducible and some changes were necessary. The method was validated and showed to be selective, specific, linear, robust, precise, and accurate. From this characterization, we concluded that pharmacopeial techniques alone are not able to detect subtle differences in active pharmaceutical ingredients; therefore, the use of other complementary techniques is required to ensure strict quality control in the pharmaceutical industry.

scholarly journals Synthesis and characterization of apatite silicated powders with wet precipitation method

2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Analytical Techniques ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wet Precipitation ◽  
Scanning Electron

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.

scholarly journals Structural and Electrochemical Properties of Lithium Nickel Oxide Thin Films

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Gyu-bong Cho ◽  
Tae-hoon Kwon ◽  
Tae-hyun Nam ◽  
Sun-chul Huh ◽  
Byeong-keun Choi ◽  
...  
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Electrochemical Properties ◽  
Discharge Capacity ◽  
Oxygen Deficiency ◽  
Oxide Phase ◽  
Rf Magnetron Sputtering ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lithium Nickel Oxide

LiNiO2thin films were fabricated by RF magnetron sputtering. The microstructure of the films was determined by X-ray diffraction and field-emission scanning electron microscopy. The electrochemical properties were investigated with a battery cycler using coin-type half-cells. The LiNiO2thin films annealed below 500°C had the surface carbonate. The results suggest that surface carbonate interrupted the Li intercalation and deintercalation during charge/discharge. Although the annealing process enhanced the crystallization of LiNiO2, the capacity did not increase. When the annealing temperature was increased to 600°C, the FeCrNiO4oxide phase was generated and the discharge capacity decreased due to an oxygen deficiency in the LiNiO2thin film. The ZrO2-coated LiNiO2thin film provided an improved discharge capacity compared to bare LiNiO2thin film suggesting that the improved electrochemical characteristic may be attributed to the inhibition of surface carbonate by ZrO2coating layer.

scholarly journals Characterising the Microstructure of an Additively Built Al-Cu-Li Alloy

Materials ◽  
2020 ◽  
Vol 13 (22) ◽  
pp. 5188
Author(s):  
Iris Raffeis ◽  
Frank Adjei-Kyeremeh ◽  
Uwe Vroomen ◽  
Silvia Richter ◽  
Andreas Bührig-Polaczek
Keyword(s):  
Volume Fraction ◽  
Analytical Techniques ◽  
High Strength ◽  
High Energy ◽  
Phase System ◽  
X Ray Diffraction ◽  
Powder Bed ◽  
X Ray ◽  
Conventional View ◽  
Multi Phase

Al-Cu-Li alloys are famous for their high strength, ductility and weight-saving properties, and have for many years been the aerospace alloy of choice. Depending on the alloy composition, this multi-phase system may give rise to several phases, including the major strengthening T1 (Al2CuLi) phase. Microstructure investigations have extensively been reported for conventionally processed alloys with little focus on their Additive Manufacturing (AM) characterised microstructures. In this work, the Laser Powder Bed Fusion (LPBF) built microstructures of an AA2099 Al-Cu-Li alloy are characterised in the as-built (no preheating) and preheat-treated (320 °C, 500 °C) conditions using various analytical techniques, including Synchrotron High-Energy X-ray Diffraction (S-HEXRD). The observed dislocations in the AM as-built condition with no detected T1 precipitates confirm the conventional view of the difficulty of T1 to nucleate on dislocations without appropriate heat treatments. Two main phases, T1 (Al2CuLi) and TB (Al7.5Cu4Li), were detected using S-HEXRD at both preheat-treated temperatures. Higher volume fraction of T1 measured in the 500 °C (75.2 HV0.1) sample resulted in a higher microhardness compared to the 320 °C (58.7 HV0.1) sample. Higher TB volume fraction measured in the 320 °C sample had a minimal strength effect.

scholarly journals Natural and Activated Allophane Catalytic Activity Based on the Microactivity Test in Astm Norm 3907/D3907M-2019

2020 ◽  
Vol 10 (9) ◽  
pp. 3035
Author(s):  
Edward Henry Jiménez Calderón ◽  
Ana Emperatriz Paucar Tipantuña ◽  
Paulina Fernanda Herrera Mullo ◽  
Daniel Alejandro Hidalgo Cháfuel ◽  
Washington Ruiz ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Bet Surface Area ◽  
Navier Stokes ◽  
Maximum Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Catalytic Activation ◽  
Atomic Force ◽  
Activating Agent

The optimal conditions of the catalytic activation of allophane were evaluated for possible use as a catalyst within a fluidized bed catalytic cracking unit (FCC). The physicochemical properties of natural allophane and activated allophane were studied by using an alkaline activating agent, followed by a hydrothermal treatment. For the characterization, analytical techniques were used: Fourier transform infrared spectroscopy, particle size, (BET) surface area, thermogravimetry (TGA), X-ray diffraction (XRD), chemisorption, X-ray fluorescence (XRF), atomic force microscopy (AFM), and chromatography. The catalytic evaluation was determined by the (MAT) micro activity test equipment constructed according to ASTM D-3907/D3907M-2019. In addition, the Navier–Stokes 3D equations (nonlinear partial derivatives) were studied, which allow studying molecular dynamics contributing substantively to chemical kinetics describing the process of decomposition of crude oil in thermal cracking, determining the maximum temperature at which it retains its properties through the action of heat.

scholarly journals Synthesis of calcium-phosphate and chitosan bioceramics for bone regeneration

2001 ◽  
Vol 73 (4) ◽  
pp. 525-532 ◽  
Author(s):  
MELLATIE R. FINISIE ◽  
ATCHE JOSUÉ ◽  
VALFREDO T. FÁVERE ◽  
MAURO C. M. LARANJEIRA
Keyword(s):  
Bone Regeneration ◽  
Solid Phase ◽  
Thermo Gravimetric Analysis ◽  
Analytical Techniques ◽  
Bone Substitutes ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Beneficial Effects ◽  
Fourier Transformed Infrared Spectroscopy

Bioceramic composites were obtained from chitosan and hydroxyapatite pastes synthesized at physiological temperature according to two different syntheses approaches. Usual analytical techniques (X-ray diffraction analysis, Fourier transformed infrared spectroscopy, Thermo gravimetric analysis, Scanning electron microscopy, X-ray dispersive energy analysis and Porosimetry) were employed to characterize the resulting material. The aim of this investigation was to study the bioceramic properties of the pastes with non-decaying behavior from chitosan-hydroxyapatite composites. Chitosan, which also forms a water-insoluble gel in the presence of calcium ions, and has been reported to have pharmacologically beneficial effects on osteoconductivity, was added to the solid phase of the hydroxyapatite powder. The properties exhibited by the chitosan-hydroxyapatite composites were characteristic of bioceramics applied as bone substitutes. Hydroxyapatite contents ranging from 85 to 98% (w/w) resulted in suitable bioceramic composites for bone regeneration, since they showed a non-decaying behavior, good mechanical properties and suitable pore sizes.

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