Surface thermal analysis

Fig. 7.10. The solid state reactivity of shock-modified zirconia with lead oxide as studied with differential thermal analysis (DTA) shows both a reduction in onset temperature and apparent increase in reaction rate. The shock-modified material has a behavior much like the much higher specific surface powder shown in B (after Hankey et al. [82H01]).

Thermal analysis techniques reveal that water is bound in opal in more than one manner. Most of the water is physically held in inclusions or microscopic pores within the opal, that is, in spaces between the microspheres. Water held in this manner can escape through complex systems of microscopic fissures or cracks, induced by temperatures even below 100°C. Some water is held within the opal via chemical bonding ( adsorption ) to the surfaces of the silica microspheres and is retained to temperatures approaching 1000°CJ7J Furthermore, since the microspheres themselves are composed of much smaller silica particles, water is additionally coated on the surfaces of these minute particles. The porous nature of opal and its thermal sensitivity require special care, for dehydration may result in cracking that greatly diminishes the value of this gemstone. 

An instrument designed to follow hysteresis losses in polymers by measuring the resistance to the rolling of small balls over the surface of the test piece it can investigate transitions in polymers to as low a temperature as -120 °C. Superseded by modem dynamic mechanical thermal analysis equipment. 

Infrared spectra, of fats and oils, 10 823 Infrared spectral region, 19 564 Infrared spectroscopy, 14 224-243 23 136-143. See also Chromatography-infrared spectroscopy Far- infrared spectroscopy ir-selective surfaces Ir (infrared) spectroscopy Near- infrared spectroscopy Thermal analysis-infrared spectroscopy applications of, 14 239-240 23 140-141 in composition measurements, 20 682 in fiber optic fabrication, 11 138 industrial applications of, 14 240 instrumentation in, 14 225-228 23 137-138... 

Another thermal analysis method available for catalyst characterization is microcalorimetiy, which is based on the measurement of the heat generated or consumed when a gas adsorbs and reacts on the surface of a solid [66-68], This information can be used, for instance, to determine the relative stability among different phases of a solid [69], Microcalorimetiy is also applicable in the measurement of the strengths and distribution of acidic or basic sites as well as for the characterization of metal-based catalysts [66-68], For instance, Figure 1.10 presents microcalorimetry data for ammonia adsorption on H-ZSM-5 and H-mordenite zeolites [70], clearly illustrating the differences in both acid strength (indicated by the different initial adsorption heats) and total number of acidic sites (measured by the total ammonia uptake) between the two catalysts. 

The elemental composition of CuCr204 Cu 27.44%, Cr 44.92%, O 27.64%. The catalyst is analysed by measurement of surface area and pore volume also by differential thermal analysis, thermogravimetric analysis and x-ray studies. 

Figure 1.1.20 shows the differential thermal analysis (DTA) data for the cores, of chromium hydrous oxides particles prepared in the absence of hematite, and of coated particles. It is obvious that the latter behave as the coating material, when alone. This example clearly indicates the possibility of having the surface site characteristics of chromium hydrous oxide induced onto ellipsoidal iron oxide particles. The latter morphology cannot be achieved by diiecl precipitation of the same chromium compound. 

R.Sh. Mikhail and E. Robens(eds.), Microstructure and Thermal Analysis of Solid Surface, Wiley Heyden Ltd., 1983. 

Thermal analysis on the materials shows that all three catalysts exhibit weight losses at about 400°C indicating that the Cr complex is chemically attached to the surface of the support. Both the imprinted catalysts exhibit similar weight losses of ... 

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