Non-crystalline hydrous feldspathoids in Late Permian carbonate rock

Clay Minerals ◽  
1991 ◽  
Vol 26 (4) ◽  
pp. 527-534 ◽  
Author(s):  
C. Bender Koch
Keyword(s):  
Electron Microscopy ◽  
Carbonate Rock ◽  
Crystalline Material ◽  
Molar Ratio ◽  
Late Permian ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selective Area ◽  
Transmission Electron ◽  
Oolitic Shoal

AbstractThe EDTA-insoluble residues from five samples (two from the oolitic shoal facies and three from the lagoonal facies) of the Late Permian Ca-2 unit (Zechstein) have been investigated by X-ray diffraction, infrared spectroscopy, and scanning and transmission electron microscopy with energy dispersive X-ray analysis (EDXA). The results show that spheres of non-crystalline hydrous feldspathoids (with Al/Si molar ratio between 1·5 and 2·2) dominate the residues of samples from the oolitic shoal facies. Samples from the lagoonal facies are dominated by crystalline material (muscovite and quartz), but two of the samples contain a small number of spheres. Analyses of these samples by selective area diffraction and EDXA revealed the presence of small amounts of non-crystalline hydrous feldspathoids with Al/Si molar ratio between 0·1 and 1·9.

scholarly journals Oxalic Acid-Assisted Hydrothermal Synthesis and Luminescent of Hexagonal NaYF4:Ln3+ (Ln = Sm, Eu, Yb/Er) Micro/Nanoplates

2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Feng Tao ◽  
Zhishun Shen ◽  
Zhijun Wang ◽  
Da Shu ◽  
Qi Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Oxalic Acid ◽  
Molar Ratio ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ph Values ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Display Systems

Hexagonal NaYF4:Ln3+ micro/nanoplates were successfully synthesized via a hydrothermal method using oxalic acid as a shape modifier. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) have been used to study the morphologies and crystal structure of the products. The effects of the pH values and the molar ratio of oxalic acid to NaOH on the crystal growth have been investigated in detail. The time-dependent experiments have been conducted to investigate the morphology evolution process, and based on the results, a possible growth mechanism was proposed. The photoluminescence properties of 5 mol% Eu3+ and 3 mol% Sm3+ doped NaYF4 and 20 mol% Yb3+/2 mol% Er3+ codoped NaYF4 micro/nanoplates were investigated. The experimental results showed that NaYF4:Ln3+ micro/nanoplates have excellent luminescence and can be potential application in the field of light display systems, lasers, and optoelectronic devices.

Convenient Route to Cu-Ag Bimetallic Nanoleaflets with High Content of Cu and their Electrochemical Properties

2017 ◽  
Vol 727 ◽  
pp. 395-402
Author(s):  
Zi Run Wang ◽  
Xin Liu ◽  
Gui Qi Xie ◽  
Yi Wu ◽  
Ming Nie ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Reduction Method ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Phase Reduction ◽  
Transmission Electron ◽  
Convenient Route

Cu-Ag alloy nanoparticles were synthesized by a liquid phase reduction method. Using sodium formaldehyde sulfoxylate (SFS) as reducing agents, copper-silver bimetallic nanoleaflets with high content of Cu were prepared. The obtained Cu-Ag bimetallic nanocrystal were characterized by powder X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), field emission scanning electron microscope (FESEM), high resolution transmission electron microscopy (HRTEM) and transmission electron microscopy (TEM). Different molar ratio of Cu-Ag bimetallic nanomaterials could produce different morphologies. The surfactant β-CD plays a crucial role on the structure of the products. The different molar ratios of Cu-Ag were also investigated. The electrochemical activity was evaluated using cyclic voltammetry (CV), electrochemical hydrogen evolution reaction (HER) in a 0.5M Na2SO4 electrolyte.

Microstructural evolution of mullites produced from single-phase gels

2007 ◽  
Vol 40 (2) ◽  
pp. 260-276 ◽  
Author(s):  
Marek Andrzej Kojdecki ◽  
Esther Ruiz de Sola ◽  
Francisco Javier Serrano ◽  
Estefanía Delgado-Pinar ◽  
María Mercedes Reventós ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Unit Cell ◽  
Molar Ratio ◽  
Model Parameters ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
X Ray ◽  
Cell Parameters ◽  
Transmission Electron ◽  
Diffraction Patterns

The crystalline microstructure of mullites obtained by heating monophasic gels has been investigated. Gels with alumina to silica molar ratio of 3:2 (as in secondary mullite) and 2:1 (as in primary mullite) were prepared by gelling mixtures of aluminium nitrate and tetraethylorthosilicate. Phase transformations were induced by heating the gel precursors, with different final treatment temperatures between 1173 and 1873 K. The mullites formed as a result of thermal treatment were studied by means of X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The crystalline structure (unit-cell parameters) and microstructure were determined from X-ray diffraction patterns. The formation of mullites of homogeneous chemical composition and with unit-cell parameters depending almost linearly on the treatment temperature was found. Their compositions, expressed as alumina to silica molar ratio, were determined from the unit-cell parameters and were in the range of those characterizing primary and secondary mullites. Mullites processed at lower temperatures were accompanied by small amounts of vitreous phase. The crystalline microstructure of the obtained mullites was interpreted by means of a mathematical model of polycrystalline material, involving prevalent crystallite shape, volume-weighted crystallite size distribution and second-order crystalline lattice strain distribution as model parameters. The model parameters were determined for each sample by modelling its X-ray diffraction pattern and fitting it to a measured pattern. Bimodality of the size distribution was observed and explained as a consequence of two crystallite nucleation and growth processes, which started from small alumina-rich and alumina-poor domains, spontaneously formed in a precursor gel at early stages of heating. Images produced by scanning and transmission electron microscopy agreed well with the characteristics obtained from the analysis of the X-ray diffraction patterns.

scholarly journals Catalytic Dry Reforming and Cracking of Ethylene for Carbon Nanofilaments and Hydrogen Production Using a Catalyst Derived from a Mining Residue

Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1069 ◽  
Author(s):  
Abir Azara ◽  
El-Hadi Benyoussef ◽  
Faroudja Mohellebi ◽  
Mostafa Chamoumi ◽  
François Gitzhofer ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Fixed Bed ◽  
Dry Reforming ◽  
Fixed Bed Reactor ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Spent Catalysts ◽  
Temperature Programmed

In this study, iron-rich mining residue (UGSO) was used as a support to prepare a new Ni-based catalyst via a solid-state reaction protocol. Ni-UGSO with different Ni weight percentages wt.% (5, 10, and 13) were tested for C2H4 dry reforming (DR) and catalytic cracking (CC) after activation with H2. The reactions were conducted in a differential fixed-bed reactor at 550–750 °C and standard atmospheric pressure, using 0.5 g of catalyst. Pure gases were fed at a molar ratio of C2H4/CO2 = 3 for the DR reaction and C2H4/Ar = 3 for the CC reaction. The flow rate is defined by a GHSV = 4800 mLSTP/h.gcat. The catalyst performance is evaluated by calculating the C2H4 conversion as well as carbon and H2 yields. All fresh, activated, and spent catalysts, as well as deposited carbon, were characterized by Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDX), transmission electron microscopy (TEM), temperature programmed reduction (TPR), and thermogravimetric analysis (TGA). The results so far show that the highest carbon and H2 yields are obtained with Ni-UGSO 13% at 750 °C for the CC reaction and at 650 °C for the DR reaction. The deposited carbon was found to be filamentous and of various sizes (i.e., diameters and lengths). The analyses of the results show that iron is responsible for the growth of carbon nanofilaments (CNF) and nickel is responsible for the split of C–C bonds. In terms of conversion and yield efficiencies, the performance of the catalytic formulations tested is proven at least equivalent to other Ni-based catalyst performances described by the literature.

Catalytic Activity of Ag-Co-MCM-41 for Liquid-Phase Selective Oxidation of Styrene to Benzaldehyde

2020 ◽  
Vol 20 (3) ◽  
pp. 1670-1677 ◽  
Author(s):  
Tingshun Jiang ◽  
Guofang Gao ◽  
Cheng Yang ◽  
YuLin Mao ◽  
Minglan Fang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Liquid Phase ◽  
Molar Ratio ◽  
Oxidizing Agent ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Adsorption Desorption ◽  
Temperature Time ◽  
Mcm 41

A series of Ag-Co-MCM-41 with different metal loadings have been synthesized through the hydrothermal method. All the prepared catalysts were characterized by N2 adsorption–desorption, X-ray diffraction analysis, transmission electron microscopy. The results revealed that the structure of MCM-41 was well preserved and Ag and Co have been introduced successfully into the mesoporous channels of MCM-41. The liquid-phase catalytic oxidation of styrene on these catalysts was investigated using H2O2 as an oxidizing agent and acetone as a solvent in thermostatic water bath. The influence of metal loading, the catalyst dose, temperature, time and styrene/oxidant molar ratio on the conversion of styrene and yield and selectivity of benzaldehyde was investigated. Also, the reusability of the catalysts was evaluated.

Size-Controllable Synthesis of Worm-Like SiO2 Microspheres Using Dodecylamine as Direct Agent in Ethanol/Water Solvent System

2013 ◽  
Vol 448-453 ◽  
pp. 154-159
Author(s):  
Xue Ling Zhang ◽  
Wei Yao Zhu ◽  
Meng Jing Cao ◽  
Qiang Cai ◽  
Xiao Feng Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Nitrogen Adsorption ◽  
Solvent System ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Controllable Synthesis ◽  
Silica Microspheres ◽  
X Ray ◽  
Water Solvent ◽  
Transmission Electron

Size-controllable synthesis of worm-like microporous monodispersed SiO2microspheres using dodecylamine (DDA) as direct agent in ethanol-water solvent system was firstly developed by varying the proportion of reactants. The products were characterized with scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), small angle X-ray diffraction (SAXRD) and nitrogen adsorption. The results showed that the SiO2microspheres with size of 50nm~1um could be prepared by varying the molar ratio of water/ethanol when the molar ratio of (DDA)/tetraethyl orthosilicate (TEOS) is 0.4 and the concentration of TEOS varied from 0.138 to 0.248mol/L. This method is simple and convenient, the prepared SiO2microspheres are monodispersed and uniform, the worm-like pore size is about 1.4nm. The size controllable silica microspheres could be used as an excellent additional medium to alter rheological behavior of fluid after surface modification..

Synthesis of ZnO at Different Atomic Proportion Produced by Chemical Precipitation

2012 ◽  
Vol 1481 ◽  
pp. 127-133
Author(s):  
A. Medina ◽  
L. Béjar ◽  
G. Herrera-Pérez
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Chemical Composition ◽  
Chemical Precipitation ◽  
Growth Direction ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wurtzite Crystal Structure ◽  
Transmission Electron

ABSTRACTZinc oxide (ZnO) nanoparticles were produced using chemical precipitation synthesis with a molar ratio of 1:1, 1:2 and 1:3. The structure, chemical composition and morphology were investigated by X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM). XRD and EDS demonstrated that the all particles formed at different atomic proportion were of wurtzite crystal structure with the same chemical composition. SEM and TEM showed the formation of hexagonal particles with a molar ratio of 1:1 while the samples synthesized with a molar ratio 1:2 and 1:3 showed a circular shape. HRTEM and Fast Fourier Transform (FFT) demonstrated that the all particles were formed with a preferable [0001] growth direction.

Synthesis of Hollow Sphere CdSe from CdCl2 Aqueous Solution Containing Ethylenediamine

2007 ◽  
Vol 336-338 ◽  
pp. 2037-2040
Author(s):  
Moon Hee Choi ◽  
Yoon Bok Lee ◽  
In Bae Kim ◽  
Young Seok Kim ◽  
Young Mok Rhyim ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Hollow Sphere ◽  
Morphological Difference ◽  
Molar Ratio ◽  
Mixed Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Sodium Selenosulfate

Cadmium selenide (CdSe) of hollow sphere with 30-50nm in diameter have been prepared form the mixed solution of cadmium chloride (CdCl2), sodium selenosulfate(Na2SeSO3) and ethylenediamine (H2NCH2CH2NH2) at room temperature. The hollow sphere of CdSe was characterized by transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD). The molar ratio of EDA to Cd2+ ions in this system was important factor on controlled synthesis in the self-encapsulated morphology. Based on the observation on morphological difference with molar ratio of EDA to Cd2+ ion, the possible mechanism for the formation of CdSe hollow sphere was discussed.

scholarly journals Synthesis of an optical catalyst for cracking contaminating dyes in the wastewater of factories using indium oxide in nanometer and usage in agriculture

2019 ◽  
Vol 21 (4) ◽  
pp. 98-105 ◽  
Author(s):  
Ishaq F. E. Ahmed ◽  
Ahmed I. El-Shenawy ◽  
Moamen S. Refat
Keyword(s):  
Electron Microscopy ◽  
Indium Oxide ◽  
Organic Dyes ◽  
Low Cost ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir ◽  
20 Nm

Abstract Herein, the photocatalytic degradation of the Congo Red (CR) and Crystal Violet (CV) dyes in an aqueous solution were discussed in the presence of an indium(III) oxide (In2O3) as optical catalyst efficiency. The caproate bidentate indium(III) precursor complex has been synthesized and well interpreted by elemental analysis, molar conductivity, Fourier transform infrared (FT-IR), UV-Vis, and thermogravimetric (TGA) with its differential thermogravimetric (DTG) studies. The microanalytical and spectroscopic assignments suggested that the associated of mononuclear complex with 1:3 molar ratio (M3+:ligand). Octahedral structure is speculated for this parent complex of the caproate anion, CH3(CH2)4COO− ligand. The In2O3 NPs with nanoscale range within 10–20 nm was synthesized by a simple, low cost and eco-friendly method using indium(III) caproate complex. Indium oxide nanoparticles were formed after calcination of precursor in static air at 600°C for 3 hrs. The structural, grain size, morphological and decolorization efficiency of the synthesized NPs were characterized using the FT-IR, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and transmission electron microscopy (TEM) analyses. It was worthy mentioned that the prepared In2O3 NPs showed a good photodegradation properties against CR and CV organic dyes during 90 min.

scholarly journals Direct Fabrication of Cobalt Oxide Nanoparticles Employing Sucrose as a Combustion Fuel

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
M. Th. Makhlouf ◽  
B. M. Abu-Zied ◽  
T. H. Mansoure
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Crystallite Size ◽  
Thermal Analyses ◽  
Combustion Method ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cobalt Oxide Nanoparticles ◽  
Transmission Electron

Combustion method has been used as a fast and facile method to prepare nanocrystalline Co3O4 spinel employing sucrose as a combustion fuel. The products were characterized by thermal analyses (TGA and DTA), X-ray diffraction technique (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) techniques. Experimental results revealed that the molar ratio of fuel/oxidizer (F/O) plays an important role in controlling the crystallite size of Co3O4 nanoparticles. Transmission electron microscopy indicated that the crystallite size of Co3O4 nanocrystals was in the range of 13–32 nm. X-ray diffraction confirmed the formation of CoO phase with spinel Co3O4. The effect of calcination temperature on crystallite size and morphology has been, also, discussed.

Sign in / Sign up

Export Citation Format

Share Document