Composites XRD

Our view of the catalyst surface is schematically depicted in Figure 4. The indirect and direct characterization data for Pt indicates that it is present in a zero valence state. The Pt will therefore be distributed among Pt atoms, Pt clusters that are larger than one atom and Pt present as a Pt/Sn alloy. Thus, a description of the state of Pt in the Pt-Sn-alumina catalyst involves determining the fraction present in each of the three states. Furthermore, both of the direct methods for determining the Pt/Sn alloy composition, XRD and TEM, indicates that only the PtSn =1 1 alloy is formed. Thus,... 

The above sections describe the occurrence of green clay minerals giving compositions, XRD characteristics, and general situations of formation. This information can be used to establish a general geochemical framework for the formation of green (iron-bearing) clay minerals. 

The bed material samples were collected from bottom ash collector of the boiler. The selected samples were studied with SEM-EDS to determinate the chemical compositions. XRD was used to study the amount of amorphous material present in the samples. 

Hunite MgjCalCOj) from Egirdir Lake, Turkey Properties elemental composition, XRD pattern available [325]. 

For the quantitative determination of ash phase composition XRD or XRD and ash extraction with hydrofluoric acid are used [113,114,123]. 

Figure 7.4 Effect of order of addition on alumina composition XRD patterns of alumina obtained by (a) 2-jet precipitation at constant pH, (b) acid to base addition, and (c) base to acid addition [18].

Aso H, Matsuoka K, Sharma A, Tomita A. Structural analysis of PVC and PEA carbons prepared at 500-1000 °C based on elemental composition, XRD and HRTEM. Carbon 2004 42(14) 2963-2973. 

Phase composition XRD studies revealed that modification of cordierite with manganese oxide results in formation of mainly cordierite-like phase at calcination temperature about 1150°C, magnesium silicate, quartz and Mn203 being the minor phases (Figure 1). It should be mentioned that the usual ceramic preparation procedure does not lead to cordierite crystallization at this temperature. The preliminary mechanical treatment of the raw materials considerably reduces the temperature and time of... 

Ogata et al. first prepared PLA/OMLS blends by dissolving the polymer in hot chloroform in the presence of dimethyl distearyl ammonium modified MMT (2C18MMT). In the case of PLA/MMT composites, XRD and SAXS results showed that the silicate layers forming the clay could not be intercalated in the... 

Characterization. Ceramic bodies are characterized by density, mass, and physical dimensions. Other common techniques employed in characterizing include x-ray diffraction (XRD) and electron or petrographic microscopy to determine crystal species, stmcture, and size (100). Microscopy (qv) can be used to determine chemical constitution, crystal morphology, and pore size and morphology as well. Mercury porosknetry and gas adsorption are used to characterize pore size, pore size distribution, and surface area (100). A variety of techniques can be employed to characterize bulk chemical composition and the physical characteristics of a powder (100,101). 

X-ray Diffraction (XRD) is a powerful technique used to uniquely identify the crystalline phases present in materials and to measure the structural properties (strain state, grain size, epitaxy, phase composition, preferred orientation, and defect structure) of these phases. XRD is also used to determine the thickness of thin films and multilayers, and atomic arrangements in amorphous materials (including polymers) and at inter ces. 

Thin-film XRD is important in many technological applications, because of its abilities to accurately determine strains and to uniquely identify the presence and composition of phases. In semiconduaor and optical materials applications, XRD is used to measure the strain state, orientation, and defects in epitaxial thin films, which affect the film s electronic and optical properties. For magnetic thin films, it is used to identify phases and to determine preferred orientations, since these can determine magnetic properties. In metallurgical applications, it is used to determine strains in surfiice layers and thin films, which influence their mechanical properties. For packaging materials, XRD can be used to investigate diffusion and phase formation at interfaces... 

Interdiffusion of bilayered thin films also can be measured with XRD. The diffraction pattern initially consists of two peaks from the pure layers and after annealing, the diffracted intensity between these peaks grows because of interdiffusion of the layers. An analysis of this intensity yields the concentration profile, which enables a calculation of diffusion coefficients, and diffusion coefficients cm /s are readily measured. With the use of multilayered specimens, extremely small diffusion coefficients (-10 cm /s) can be measured with XRD. Alternative methods of measuring concentration profiles and diffusion coefficients include depth profiling (which suffers from artifacts), RBS (which can not resolve adjacent elements in the periodic table), and radiotracer methods (which are difficult). For XRD (except for multilayered specimens), there must be a unique relationship between composition and the d-spacings in the initial films and any solid solutions or compounds that form this permits calculation of the compo-... 

One must be sure of the purity of the model compound. It may have deteriorated (for example, by reaction or water absorption), its surface may not have the same composition as the bulk, or it may not be of the correct crystallographic phase. It is tempting to use single crystals to be sure of the geometric structure, but noncubic crystals give angle-dependent spectra. The crystallography of any compound should be checked with XRD. 

For Sm, Eu, and Yb, on the other hand, nanocapsules containing carbides were not found in the cathode deposit by either TEM or XRD. To see where these elements went, the soot particles deposited on the walls of the reaction chamber was investigated for Sm. XRD of the soot produced from Sm203/C composite anodes showed the presence of oxide (Sm203) and a small amount of carbide (SmC2). TEM, on the other hand, revealed that Sm oxides were naked, while Sm carbides were embedded in flocks of amorphous carbon[12J. The size of these compound particles was in a range from 10 to 50 nm. However, no polyhedral nanocapsules encaging Sm carbides were found so far. 

Film-forming chemical reactions and the chemical composition of the film formed on lithium in nonaqueous aprotic liquid electrolytes are reviewed by Dominey [7], SEI formation on carbon and graphite anodes in liquid electrolytes has been reviewed by Dahn et al. [8], In addition to the evolution of new systems, new techniques have recently been adapted to the study of the electrode surface and the chemical and physical properties of the SEI. The most important of these are X-ray photoelectron spectroscopy (XPS), SEM, X-ray diffraction (XRD), Raman spectroscopy, scanning tunneling microscopy (STM), energy-dispersive X-ray spectroscopy (EDS), FTIR, NMR, EPR, calorimetry, DSC, TGA, use of quartz-crystal microbalance (QCMB) and atomic force microscopy (AFM). 

The nano-scale structures in polymer layered-silicate nano-composites can be thoroughly characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). XRD is used to identify intercalated structures. XRD allows quantification of changes in layer spacing and the most commonly used to probe the nano-composite structure and... 

PLA/PCL-OMMT nano-composites were prepared effectively using fatty amides as clay modifier. The nano-composites shows increasing mechanical properties and thermal stability (Hoidy et al, 2010c). New biopolymer nano-composites were prepared by treatment of epoxidized soybean oil and palm oil, respectively plasticized PLA modified MMT with fatty nitrogen compounds. The XRD and TEM results confirmed the production of nanocomposites. The novelty of these studies is use of fatty nitrogen compoimds which reduces the dependence on petroleum-based surfactants (Al-Mulla et al., 2011 Al-Mulla et ah, 2011 Al- Mulla et ah, 2010c). 

This is a nonpolar rubber with very little unsamration. Nanoclays as well as nanotubes have been used to prepare nanocomposites of ethylene-propylene-diene monomer (EPDM) rubber. The work mostly covers the preparation and characterization of these nanocomposites. Different processing conditions, morphology, and mechanical properties have been smdied [61-64]. Acharya et al. [61] have prepared and characterized the EPDM-based organo-nanoclay composites by X-ray diffracto-gram (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy... 

The properties of titania particles were investigated using X-ray diffraction (XRD, Model D/MAX-RB, Rigaku Ltd.), scanning electron microscopy (SEM, Model 535M, Philips Ltd.), transmission electron microscopy (TEM, Model 2000EX, JEOL Ltd.). The crystallite sizes were estimated by Scherrer s equation and the composition of rutile phase in titania were estimated from the respective integrated XRD peak intensities. 

As illustrated by Eig. 4.13, an electron microscope offers additional possibilities for analyzing the sample. Diffraction patterns (spots from a single-crystal particle and rings from a collection of randomly oriented particles) enable one to identify crystallographic phases as in XRD. Emitted X-rays are characteristic for an element and allow for a determination of the chemical composition of a selected part of the sample. This technique is referred to as energy-dispersive X-ray analysis (EDX). 

The second approach is to study real catalysts with in situ techniques such as infrared and Mossbauer spectroscopy, EXAFS and XRD, under reaction conditions, or, as is more often done, under a controlled environment after quenching of the reaction. The in situ techniques, however, are not sufficiently surface specific to yield the desired atom-by-atom characterization of the surface. At best they determine the composition of the particles. 

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