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.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Characterization of chitin preparations using powder and film X-ray diffraction methods

2013 ◽  
Vol 28 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Jeffrey R. Deschamps
Keyword(s):  
Diffraction Pattern ◽  
Purification Procedure ◽  
Limited Extent ◽  
X Ray Diffraction ◽  
X Ray ◽  
Naturally Occurring ◽  
Natural Polysaccharide ◽  
Different Sources

Chitin is a natural polysaccharide found in many diverse phyla and almost always occurs in association with protein. In this study the chitin polymer is characterized by X-ray diffraction from its naturally occurring unprocessed state through various steps used in the purification procedure. In addition, the effect of different treatments on the final product is examined. These studies show that native chitin has a characteristic diffraction pattern that is not altered by the mild treatments used to isolate relatively pure chitin. Chitins prepared from different sources exhibit the same characteristic diffraction pattern. In addition, chitin films prepared using non-degrading solvents retain most of the characteristic patterns. De-acylation of chitin to produce chitosan results in large changes to the diffraction pattern. To a very limited extent features present in the diffraction pattern of native chitin can be recovered by re-acylation of chitosan.

Mechanochemical Synthesis of Magnesium Doped Hydroxyapatite: Powder Characterization

2013 ◽  
Vol 372 ◽  
pp. 62-65 ◽  
Author(s):  
Sharifah Adzila ◽  
Singh Ramesh ◽  
Iis Sopyan ◽  
C.Y. Tan ◽  
Mohd. Hamdi ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Present Method ◽  
X Ray Diffraction ◽  
Mechanochemical Method ◽  
Xrd Pattern ◽  
X Ray ◽  
Hydroxyapatite Powder ◽  
Powder Properties ◽  
Mg Doped

In this study, the mechanochemical method was employed to synthesize hydroxyapatite (HA) and magnesium (Mg) doped hydroxyapatite (HA) powders. The effect of Mg2+ into the synthesized HA powder properties were investigated. Characterization of the synthesized HA and Mg doped HA at various concentrations (1% - 5% MgHA) were accomplished through X-ray diffraction (XRD) and Fourier transform infrared (FTIR) analyses. nanosize of HA and Mg doped HA powders were successfully synthesized through the present method as indicated from the different peaks intensity and adsorption bands obtained in XRD pattern and FTIR respectively.

Preparation and Characterization of Clays from Different Areas in Ban Bo Suak, Nan Province, Thailand

2015 ◽  
Vol 659 ◽  
pp. 127-131
Author(s):  
Usanee Malee ◽  
Sakdiphon Thiansem
Keyword(s):  
Clay Sample ◽  
X Ray Diffraction ◽  
Scientific Process ◽  
Quartz Content ◽  
Xrd Pattern ◽  
X Ray ◽  
Kiln Site ◽  
Before And After ◽  
Tone Color

The scientific process was used to explain characterization and physical properties of the clay sample close to the ancient Nan kiln site. These samples were obtained from JQA, FQB, PQC and NQD. X-ray diffraction (XRD) and X-ray fluorescence (XRF) technique were used to determine the chemical composition and phase transformation before and after fired at 800-1250 °C. XRF result was confirmed that all clay samples mainly contained SiO2(>80 wt. %) XRD pattern indicated that quartz was the majority of phase in the all of them. High amount of Fe2O3(>1.6 wt. %) was related to the red-brown tone color. The clay sample could be fired up to 1280 °C without wrapping behavior; it was found that FQB clay had the highest firing resistance due to the maximum quartz content.

Physical and Chemical Properties of Mineral in Soils of Cassava Cropping Area: A Case Study in Chonburi Province

2014 ◽  
Vol 979 ◽  
pp. 440-443
Author(s):  
W. Siriprom ◽  
K. Teanchai ◽  
S. Kongsriprapan ◽  
J. Kaewkhao ◽  
N. Sangwaranatee
Keyword(s):  
Thermo Gravimetric Analysis ◽  
Chemical Properties ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Physical And Chemical ◽  
And Chemical Properties

The chemical and physical properties of topsoil and subsoil which collected from the cassava cropping area in Chonburi Province have been investigated. The characterization of both soil sample were used X-Ray Diffraction (XRD), Energy Dispersive X-Ray Fluorescence (EDXRF) while FTIR used to confirmed the formation of intermolecular bonding and Thermo-Gravimetric Analysis (TGA) used for investigated the crystalline. It was found that, the XRD pattern indicated quartz phase. The chemical composition by XRF reported that the soils samples consist of Si, Al, Ca, Fe, K, Mn, Ti, Cr, Zn, Ag and Cu. and TGA results, noticed that the removal of moisture and organics material.

Synthesis and Characterization of Superparamagnetic NiFe2O4 Nanoparticles

2010 ◽  
Vol 663-665 ◽  
pp. 1325-1328 ◽  
Author(s):  
De Hui Sun ◽  
De Xin Sun ◽  
Yu Hao
Keyword(s):  
Room Temperature ◽  
Size Range ◽  
X Ray Diffraction ◽  
Inverse Spinel ◽  
Cubic Crystal ◽  
Xrd Pattern ◽  
X Ray ◽  
Nife2o4 Nanoparticles ◽  
Average Size

The superparamagnetic NiFe2O4 nanoparticles were synthesized using a hydrothermal technology through P123 sphere micelles as ‘nanoreactor’ in this work. Their morphologies, structures, surface properties and magnetism were characterized by FE-SEM, XRD, FTIR, and VSM, respectively. The nickel ferrite samples are nearly spherical and homogeneous nanoparticles with average size range of about 50-120 nm. They possess superparamagnetism at room temperature and higher saturation magnetization. X-ray diffraction (XRD) pattern confirms that the samples belong to the cubic crystal system with an inverse-spinel structure. Fourier transform infrared (FTIR) absorption spectrum indicates that the NiFe2O4 nanoparticles are stabilized by the P123 adsorbed on the surface of nanoparticles.

Synthesis and characterization of a silylated Brazilian clay mineral surface

2014 ◽  
Vol 68 (7) ◽  
Author(s):  
Márcia Silva ◽  
Saloana Gomes ◽  
Maria Fonseca ◽  
Kaline Sousa ◽  
José Espínola ◽  
...  
Keyword(s):  
Clay Mineral ◽  
Solid State Nmr ◽  
Textural Properties ◽  
Hydroxyl Groups ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Diffraction Patterns ◽  
Trimethoxy Silane

AbstractClay mineral containing kaolinite, illite and montmorillonite was organofunctionalized with silylating agents: (3-aminopropyl)triethoxysilane, 3-[2-(2-aminoethylamino)ethylamino]propyl-trimethoxysilane and (3-mercaptopropyl)trimethoxy-silane, to yield three hybrids labelled Clay1, Clay2 and Clay3, respectively. These solids were characterized using elemental analysis, thermogravimetry, X-ray diffractometry, infrared spectroscopy, scanning electron micrograph, and 29Si and 27Al solid state NMR. Immobilized quantities of the organic groups were 0.66 mmol g−1, 0.48 mmol g−1 and 0.88 mmol g−1 for Clayx (x = 1–3), respectively. X-ray diffraction patterns confirmed the immobilization of silanes onto the surface without changes in the textural properties of the clay mineral as noted from the SEM images. Spectroscopic measurements were in agreement with the covalent bonding between the silanes and the hydroxyl groups deposited on the surface. The new hybrids were utilized as adsorbents of cobalt in aqueous solution, with retention values of 0.78 mmol g−1, 1.1 mmol g−1 and 0.70 mmol g−1 for Clayx (x = 1–3), respectively.

Surface Modification of Multi-Walled Carbon Nanotube Using Double-Chained Quartenary Ammonium Bromide

2016 ◽  
Vol 701 ◽  
pp. 18-22 ◽  
Author(s):  
Mohd Junaedy Osman ◽  
Wan Md Zin Wan Yunus ◽  
Keat Khim Ong ◽  
Noor Azilah Mohd Kasim ◽  
Siti Hasnawati Jamal ◽  
...  
Keyword(s):  
Carbon Nanotube ◽  
Functional Group ◽  
Ammonium Bromide ◽  
New Materials ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Weight Losses ◽  
Multi Walled Carbon Nanotube

Modification of multi-walled carbon nanotube (MWCNT) plays an important role to produce MWCNT crossbreeds that may be useful for exploration of new materials. In this report, characterization of dimethyl dioctadecylammonium bromide (DDOAB) modified multi-walled carbon nanotube (Mo-MWCNT) using Fourier Transform Infrared (FTIR) spectroscopy and Thermogravimetric analysis (TGA) and X-ray diffraction (XRD) is described. FTIR shows the presence of both aliphatic (CH stretching and CH bending) and ammonium (CN stretching) groups from DDOAB and the existence of C=C aromatic functional group from the structure of MWCNT in Mo-MWCNT spectra. This result was supported by TGA result which suggests that there are weight losses due to the degradation of DDOAB (between 250 °C to 500 °C) in the product. In addition, XRD pattern remain after modification suggesting attachment of MWCNT and DDOAB occurs at the surface of MWCNT.

Microstructural Investigation and Characterization of Bulk Brass Melted by Conventional and Microwave Processing Methods

2017 ◽  
Vol 890 ◽  
pp. 356-361 ◽  
Author(s):  
Lingappa M. Shashank ◽  
M.S. Srinath ◽  
Hassan Jayaraj Amarendra
Keyword(s):  
Microwave Processing ◽  
Microwave Oven ◽  
Conventional Heating ◽  
Metallic Materials ◽  
X Ray Diffraction ◽  
Microstructural Investigation ◽  
Xrd Pattern ◽  
X Ray ◽  
Domestic Microwave Oven

Microwave processing of bulk metallic materials is an emerging area. In the present work, brass in bulk form is melted in a modified domestic microwave oven operating at 2.45 GHz frequency. As-received and the as-cast brass are subjected to metallurgical and mechanical characterization. Specimens’ surface morphology is studied under Scanning Electron Microscope (SEM). X-Ray Diffraction (XRD) pattern shows the presence of copper oxides phase in both cast brass. Average tensile strength of brass melted using microwave oven is found higher when compared with brass melted in muffle furnace. Hardness of the as-cast brass is found to be higher than the as-received brass. However, brass cast by microwave irradiation exhibits around 2 % higher hardness than the brass cast by conventional heating. Microwave melting of brass consumed nearly six times less time compared to conventional melting.

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