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Powders degassing

In the dynamic method the powder is flushed with an inert gas during degassing, nitrogen is then adsorbed on the powder in a carrier of helium gas at known relative pressure while the powder is in a container surrounded by hquid nitrogen. The changing concentration of nitrogen is measured by a cahbrated conductivity cell so that the amount adsorbed can be determined. [Pg.1828]

The method uses the adsorption isotherm and the expt details of determining this may be summarized as follows (1) the powder under investigation is thoroughly degassed in a vacuum ... [Pg.529]

For routine studies with the ESR spectrometer, it is most convenient to work at X-band frequencies ( 9.5 MHz or 3 cm). The sample is usually contained in a 4 or 5 mm diameter quartz tube having a sensitive region about 2 cm in length. An alternative frequency is at Q-band ( 35,000 MHz or 1 cm). Here, the cavity dimensions are much smaller and the diameter of the sample tube is less than 2 mm. This creates some problems in handling and degassing powder samples. By varying the frequency it is possible to determine which features in a spectrum are due to Zeeman interactions... [Pg.283]

The chemical compositions of the samples were obtained by ICP in a Varian 715-ES ICP-Optical Emission Spectrometer. Powder X-ray diffraction was performed in a Philips X pert diffractometer using monochromatized CuKa. The crystallinity of the zeolites was obtained from the intensity of the most intense reflection at 23° 20 considering the parent HZ5 sample as 100% crystalline. Textural properties were obtained by nitrogen physisorption at -196°C in a Micromeritics ASAP 2000 equipment. Surface areas were calculated by the B.E.T. approach and the micropore volumes were derived from the corresponding /-plots. Prior to the adsorption measurements the samples were degassed at 400°C and vacuum overnight. [Pg.322]

After the reaction is completed, the suspension is transferred to a degassing tank, where steam is used to strip out the unreacted VCM. The PVC, now in a slurry with PVA, is separated by centrifuging and drying. The PVC powder or granules are then ready for additives and plasticizers for fabrication into one of the three mediums in which its used calendered products, extrusion, and molded products. [Pg.351]

A powder coating is the result of the application of a powder binder system, which generally consists of a resin, a crosslinker, flow additives, degassing agents, pigments or dyes, charge control agents, etc. Such a binder system is ap-pHed to the substrate as a fine, extruded powder (Fig. 20, step A), then melted at... [Pg.63]

The densities of polymers can be determined by the pyknometer technique or by the flotation method. In the pyknometer technique the liquid volume displaced by the polymer sample is determined by weighing. Most polymers have a density larger than that of water, which can, therefore, be used as the liquid. Polymers in the form of powders or pressed discs tend to adsorb or occlude air bubbles, which can lead to serious errors. This can be largely prevented by careful degassing of the pyknometer and polymer sample under vacuum before filling with liquid, and/or by addition of a small amount (0.1%) of commercial detergent to lower the surface tension of the water. [Pg.118]

The recovered Inij can be used without further purification to generate additional Ini. Procedure B was repeated with recovered Inij (14.4 g, 29.1 mmol), indium powder (1.7 g, 14.8 mmol) and degassed xylenes (320 ml) to yield 5.0 g (95%) of indium(l) iodide and 10.0 g (93%) of recovered indium(lll) iodide. [Pg.33]

Soxhlet Extraction Analysis. Powdered samples of GMC were degassed and sealed under vacuum into pyrex tubes, and irradiated at room temperature (25-30 °C) in a Cobalt-60 Gammacell. The dose rate determined by Fricke dosimetry was 0.24 Mrad/hr. Doses up to 20 Mrad were utilized. After irradiation, the tubes were opened and the samples placed in cellulose thimbles. A Soxhlet extraction was performed with methylethyl ketone at 76 1°C for 18-20 hrs. The insoluble material was dried to constant weight and the gel fraction calculated from initial weight. [Pg.243]


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