Comparison Characterization of Geopolymer Source Materials for Coating Application

2015 ◽  
Vol 754-755 ◽  
pp. 664-670 ◽  
Author(s):  
Noor Fifinatasha ◽  
Mohd Mustafa Al Bakri Abdullah ◽  
Che Mohd Ruzaidi Ghazali ◽  
Kamarudin Hussin ◽  
Mohammed Binhussain ◽  
...  
Keyword(s):  
Particle Morphology ◽  
Silica Sand ◽  
High Tech ◽  
Material Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Coating Application ◽  
Source Materials ◽  
White Clay

Geopolymer is new binder manufactured from an aluminosilicate source materials synthesized of geopolymer by polycondensation reaction of geopolymeric precursor and alkali polysilicate. Material contains mostly Silicon (Si) and Aluminium (Al) in amorphous form is a possible to be geopolymer source material. Several minerals and industrial by-product materials have been investigated geopolymer materials essentially as a replacement for Ordinary Portland Cement (OPC) and for advanced high-tech composites, ceramic applications, and also as an inorganic polymer coating. This paper reports microstructure properties of various geopolymer properties which are kaolin, white clay and silica sand, from Saudi Arabia by conducting several tests. The characterization and particle morphology of the various geopolymer sources materials was determined using scanning electron microscopy (SEM). X-Ray Fluorescence (XRF) is conducted according to perform elemental analysis and chemical analysis while X-ray Diffraction Analysis (XRD) investigates crystalline material structure, including atomic arrangement, crystalline size, and imperfections.

Sol-Gel Synthesis and Characterization of Nanocrystalline Bi4Ti3O12 Powders

2014 ◽  
Vol 997 ◽  
pp. 359-362 ◽  
Author(s):  
Chun Hong Ma ◽  
Xue Lin ◽  
Liang Wang ◽  
Yong Sheng Yan
Keyword(s):  
Phase Inversion ◽  
Bismuth Titanate ◽  
Sol Gel ◽  
Tetrabutyl Titanate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Synthesis ◽  
Source Materials

Nanocrystalline bismuth titanate (Bi4Ti3O12; BTO) powders were successfully prepared by the sol-gel method, using bismuth nitrate (Bi(NO3)3·5H2O) and tetrabutyl titanate (Ti(OC4H9)4) as source materials, acetic anhydride and ethanediol as solvents. The thermal decomposition and phase inversion process of the gel precursors were studied by using differential thermal analysis (DTA). The crystal structures and microstructures of BTO powders were investigated by using x-ray diffraction (XRD), and transmission electron microscope (TEM). The crystallization of amorphous bismuth titanate has been discussed. The effect of sintering temperature on the structure and morphology of BTO was investigated. At 644 oC and above, BTO powder undergoes a phase transformation from tetragonal to orthorhombic. At 900 oC, the purified orthorhombic BTO nanocrystals were obtained.

Analysis of LiFePO4 Cathodic Active Material Synthesized in Open Environment Conditions through Ionic Medium

2015 ◽  
Vol 1774 ◽  
pp. 1-6
Author(s):  
Darren W. Kwee ◽  
Taehoon Lim ◽  
Alfredo Martinez-Morales
Keyword(s):  
Ionic Liquid ◽  
Active Material ◽  
Particle Morphology ◽  
Time Dependent ◽  
X Ray Diffraction ◽  
X Ray ◽  
Open Environment ◽  
Scanning Electron ◽  
Ionic Liquid Medium

ABSTRACTIn this work, LiFePO4 (LFP) particles were synthesized through an ionic liquid medium. Through the fabrication of LFP particles, we observed the formation of quasi-1−dimensional (1D) structures. The characterization of phases found in the reaction, through time-dependent studies, have led us to propose a possible scheme for particle formation.Synthesized material was characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and x-ray diffraction (XRD). We also report our analysis on particle morphology and crystallinity of LFP particles synthesized through an ionic liquid−mediated process.

scholarly journals Synthesis and characterization of four new halloysite–TiO2 nanocomposites.

2013 ◽  
Vol 47 (1) ◽  
pp. 407
Author(s):  
D. Papoulis ◽  
S. Komarneni ◽  
D. Toli ◽  
D. Panagiotaras ◽  
S. Bakalis
Keyword(s):  
Sol Gel ◽  
Particle Morphology ◽  
Anatase Tio2 ◽  
Total Reflection ◽  
Attenuated Total Reflection ◽  
Published Data ◽  
X Ray Diffraction ◽  
X Ray ◽  
Tio2 Particles

The synthesis as well as the characterization of small-sized TiO2 particles supported on Halloysite are presented. Hallloysite from Utah, USA as well as from Limnos, island Greece, were used to synthesize two nanocomposites for each halloysite with TiO2 to halloysite weight ratios of 80: 20 and 60:40 and compare with published data of well formed nanocomposites of intermediate proportion (70-30) that were previously studied. All nanocomposites were prepared by deposition of anatase (TiO2) on the halloysite tubes using a sol–gel method under hydrothermal treatment at 180 °C. Phase composition, particle morphology and physical properties of these samples were characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Attenuated Total Reflection using Fourier Transform Infrared spectroscopy (ATR-FTIR) and N2 surface area analysis by BET. Preparation of all halloysite–TiO2 nanocomposites led to the anticipated good dispersion of anatase particles on halloysite surfaces. ATR-FTIR results revealed the formation of hydrogen bonding between anatase and the outer surfaces of halloysite tubes. All halloysite-TiO2 nanocomposites largely showed interparticle mesopores of about 5.7nm and high SSAs.

Quality Characterization of Iron Dust Exhaust Thermal as Alternative Ceramic Coating Raw Materials in a Brazilian Company

2014 ◽  
Vol 1077 ◽  
pp. 135-138
Author(s):  
Luiz Oliveira Veriano dalla Valentina ◽  
Marilena Valadares Folgueras ◽  
Wanessa Rejane Knop ◽  
Maria Cristina Pacheco do Nascimento ◽  
Glaucia Aparecida Prates
Keyword(s):  
Ceramic Coating ◽  
Raw Materials ◽  
Ceramic Materials ◽  
Raw Material ◽  
Silica Sand ◽  
Commercial Application ◽  
X Ray Diffraction ◽  
X Ray ◽  
Materials Used

As the raw materials used in the ceramic materials manufacturing are natural, it is important to use them as a alternative materials, thus decreasing the elements demand taken from nature. This paper aims the characterization of foundry solid powder exhaust from a brazilian company located in Joinville - SC as an alternative raw material for ceramic coating by X-ray diffraction (XRD), thermal analysis (DSC) and thermogravimetric (TG). The dust depletion is caused in the manufacturing mold sand process, when the bentonita (clay), silica sand and coal during the metal parts production are mixed in green sand production. The raw materials were characterized through X-ray diffraction (XRD), thermal (DSC) and thermogravimetric analisys (TG). The atomized powder thermogravimetric analysis curve shows three intervals associated with the mass loss and it is typical of clay commercial application.

Determination of Crystal Structure and Cation Distribution in Thin Films

1991 ◽  
Vol 35 (A) ◽  
pp. 151-157
Author(s):  
G. Will ◽  
T. C. Huang ◽  
F. Sequeda
Keyword(s):  
Crystal Structure ◽  
Thin Films ◽  
Grazing Incidence ◽  
High Tech ◽  
X Ray Diffraction ◽  
X Ray ◽  
Depth Profiles ◽  
Scanning Geometry

The structural characterization of thin films is important for research development and manufacturing of electronic, magnetic, optical, and other high-tech materials. The grazing incidence X-ray diffraction technique has bean used successfully for the determination of crystalline phases, structural-depth profiles, crystallite size, and strain, etc. of thin films with thickness's down to a few tens of Å, If the crystal structure, e.g. the distribution of atoms in the unit cell, or the crystallinity and texture (or preferred orientation) of a film is of interest, the conventional Bragg-Brentano diffractometer technique with the θ-2θ scanning geometry has been found to be appropriate.

Preparation and Characterization of Spherical Metal Particles by Spray Pyrolysis

2009 ◽  
Vol 421-422 ◽  
pp. 558-561
Author(s):  
Takayuki Kodera ◽  
Kenichi Myoujin ◽  
Takashi Ogihara
Keyword(s):  
Particle Morphology ◽  
Metal Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fine Powders ◽  
Aerosol Process ◽  
Crystal Phases ◽  
Xrd Patterns ◽  
Production Apparatus

Ag and Ni spherical fine powders were continuously produced by carrying out an aerosol process in a mass nanopowder production apparatus. The particles size, particle morphology, crystal phases and crystallinity of the as-prepared powders were characterized by a scanning electron microscope (SEM) and X-ray diffraction (XRD). The particles were nonaggregated and they exhibited a spherical morphology with a narrow size distribution. The average sizes of Ag and Ni particles were 500 nm and 700 nm, respectively. The crystallinity of the as-prepared powders was high. The XRD patterns showed that the crystal phases of the as-prepared powders were the same as those of their respective metals.

Synthesis and Characterization of Zero-Valent Iron Nanoparticles

2015 ◽  
Vol 1112 ◽  
pp. 62-65 ◽  
Author(s):  
Eka Sri Yusmartini ◽  
Dedi Setiabudidaya ◽  
Ridwan ◽  
Marsi ◽  
Faizal
Keyword(s):  
Electron Microscopy ◽  
Surface Area ◽  
Bet Surface Area ◽  
Material Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Process Characterization ◽  
Transmission Electron ◽  
Zero Valent Iron Nanoparticles

Nanoparticles, particles of size 10-9have a high potential as water, waste water and air pollution treatment. In this research, nanoscale iron particles were synthesized by reduction of Fe2SO47 H2O by NaBH4at low temperature to avoid oxidation during the process. Characterization of the particles based on particle size, material structure, surface morphology and the composition of forming element was done by transmission electron microscopy (TEM), X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectometry (EDS), respectively. Surface area and magnetic character was measured by BET surface area and vibrating sample magnetometry (VSM), respectively. Morfological observation showed that structured core-shell of size < 44 nm and shell of size ~ 3 nm with saturated magnetization value ~ 132 emu g‾¹ has been formed.

scholarly journals Preparation of Silica Gel Obtained From Early Cretaceous Sidi Aich Sands (Central Tunisia)

2021 ◽  
Author(s):  
Khalil Lazaar ◽  
Robert Pullar ◽  
Walid Hajjaji ◽  
Fakher Jamoussi
Keyword(s):  
Silica Gel ◽  
Physical Adsorption ◽  
Silica Gels ◽  
Silica Sand ◽  
X Ray Diffraction ◽  
Mineralogical Characterization ◽  
X Ray ◽  
Central Tunisia ◽  
Surface Areas

Abstract The study describes the chemical–mineralogical characterization of Barremian sand deposits. These Sidi Aich sands were collected in central Tunisia. The collected raw silica sand from the Jebel Meloussi (central Tunisia) was characterised by different techniques, such as X-ray diffraction (XRD), X-ray fluorescence (XRF) and scanning electron microscopy (SEM). X-ray diffraction showed a predominance of quartz and potassic feldspars and lower amounts of kaolinite and calcite. The obtained silica gels had pore diameters over 20 Å and specific surface areas up to 183 m2/g, close to those reported for commercial silica gel materials. The N2 adsorption isotherms have shown that new materials synthesised from Tunisian silica sands are mesoporous materials with high chemi-physical adsorption capabilities.

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.

High Resolution Replication of Organoclay Surfaces

1982 ◽  
Vol 40 ◽  
pp. 576-577
Author(s):  
W. W. Barker ◽  
W. E. Rigsby ◽  
V. J. Hurst ◽  
W. J. Humphreys
Keyword(s):  
Clay Mineral ◽  
Organic Molecule ◽  
Organic Molecules ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Naturally Occurring ◽  
Silicate Layers ◽  
Mineral Identification

Experimental clay mineral-organic molecule complexes long have been known and some of them have been extensively studied by X-ray diffraction methods. The organic molecules are adsorbed onto the surfaces of the clay minerals, or intercalated between the silicate layers. Natural organo-clays also are widely recognized but generally have not been well characterized. Widely used techniques for clay mineral identification involve treatment of the sample with H2 O2 or other oxidant to destroy any associated organics. This generally simplifies and intensifies the XRD pattern of the clay residue, but helps little with the characterization of the original organoclay. Adequate techniques for the direct observation of synthetic and naturally occurring organoclays are yet to be developed.

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