Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Particle size microscopic

In general, it appears that the Micromerograph, provided that frequent calibration checks are performed, is a good, reproducible instrument for size measurement. The operator time involved is less than with most other methods, and the calcns are not complicated. As in all sedimentation methods, only when the sample particles are spherical does the Stokes diameter that is measured become a measure of absolute particle size. Microscopic examination should be used to check on particle shape and the effect of deagglomeration... [Pg.520]

One of the most important uses of specific surface determination is for the estimation of the particles size of finely divided solids the inverse relationship between these two properties has already been dealt with at some length. The adsorption method is particularly relevant to powders having particle sizes below about 1 pm, where methods based on the optical microscope are inapplicable. If, as is usually the case, the powder has a raiige of particle sizes, the specific surface will lead to a mean particle size directly, whereas in any microscopic method, whether optical or electron-optical, a large number of particles, constituting a representative sample, would have to be examined and the mean size then calculated. [Pg.37]

Most tests of the validity of the BET area have been carried out with finely divided solids, where independent evaluation of the surface area can be made from optical microscopic or, more often, electron microscopic observations of particle size, provided the size distribution is fairly narrow. As already explained (Section 1.10) the specific surface obtained in this way is related to the mean projected diameter through the equation... [Pg.63]

Mercuric Oxide. Mercuric oxide[21908-53-2] HgO, is a red or yellow water-insoluble powder, rhombic in shape when viewed microscopically. The color and shade depend on particle size. The finer particles (< 5 -lm) appear yellow the coarser particles (> 8 -lm) appear redder. The product is soluble in most acids, organic and inorganic, but the yellow form, which has greater surface area, is more reactive and dissolves more readily. Mercuric oxide decomposes at 332°C and has a high (11.1) specific gravity. [Pg.113]

Microscopic identification models ate similar to the CMB methods except that additional information is used to distinguish the source of the aerosol. Such chemical or morphological data include particle size and individual particle composition and are often obtained by electron or optical microscopy. [Pg.379]

Comparison of Microscopic Method of Particle Size Analysis — Tungsten M-10. ... [Pg.14]

Comparison of microscopic particle size distribution with the average distribution of four identical runs made with the Coulter Counter... [Pg.14]

A procedure for proplnts is presented by J.W. French (Ref 27), who used both OM and EM (electron microscope) to study plastisol NC curing. He found that the cure time of plastisol NC is a logarithmic function of temp, and direct functions of chemical compn and total available surface area, as well as of particle size distribution. It should be noted that extensive use of statistics is required as a time-saving means of interpreting particle size distribution data. The current state-of-the-art utilizes computer techniques to perform this function, and in addition, to obtain crystal morphology data (Ref 62)... [Pg.144]

Kaye, An Electron Microscope Method for the Determination of the Particle Size Distribution and Particle Shape of Colloidal and Ball-Milled Lead Azide , PATR 2133 (1955) 25a) A.T. [Pg.147]

Before beginning a size determination, it is customary to look at the material, preferably under a microscope. This examination reveals the approx size range and distribution of the particles, and especially the shapes of the particles and the degree of aggregation. If microscopic examination reveals that the ratios between max and min diameters of individual particles do not exceed 4, and indirect technique for particle size distribution based on sedimentation or elutria-tion may be used. Sedimentation techniques for particle size determination were first used by Hall (Ref 2) in 1904, He showed that the rate of fall of individual particles in a fluid was directly related to the particle size by the hydrodynamic... [Pg.497]

The-results of the microscopic particle size determination are shown in Fig 22... [Pg.524]

Johnson, Christian, and Tiedemann (Ref 27) evaluated the Sorptometer vs the Micromero-graph and the microscope for particle size and surface area determinations to characterize powdered materials used in solid propints. Table 12 compares the surface area of A1 powder samples calculated from Micromerograph and microscopic data with that measured using a Sorptometer... [Pg.530]

If the phases present can be unambiguously identified, microscopy can be used to determine the geometry of interface initiation and advance, and to provide information about particle sizes of components of mixed reactants in a powder. Problems of interpretation arise where materials are poorly crystallized and where crystallites are small, opaque, porous or form solid solutions. With the hot-stage microscope, the progress of reactions can be followed in some instances and the occurrence of sintering and/or melting detected. [Pg.38]

K2C03 3 H202 contains hydrogen peroxide of crystallization and the solid phase decomposition involves the production of the free radicals OH and HOi, detected by EPR measurements [661]. a—Time curves were sigmoid and E = 138 kJ mole-1 for reactions in the range 333—348 K. The reaction rate was more rapid in vacuum than in nitrogen, possibly through an effect on rate of escape of product water, and was also determined by particle size. From microscopic observations, it was concluded that centres of decomposition were related to the distribution of dislocations in the reactant particles. [Pg.151]

The Fe-B nanocomposite was synthesized by the so-called pillaring technique using layered bentonite clay as the starting material. The detailed procedures were described in our previous study [4]. X-ray diffraction (XRD) analysis revealed that the Fe-B nanocomposite mainly consists of Fc203 (hematite) and Si02 (quartz). The bulk Fe concentration of the Fe-B nanocomposite measured by a JOEL X-ray Reflective Fluorescence spectrometer (Model JSX 3201Z) is 31.8%. The Fe surface atomic concentration of Fe-B nanocomposite determined by an X-ray photoelectron spectrometer (Model PHI5600) is 12.25 (at%). The BET specific surface area is 280 m /g. The particle size determined by a transmission electron microscope (JOEL 2010) is from 20 to 200 nm. [Pg.389]


See other pages where Particle size microscopic is mentioned: [Pg.580]    [Pg.65]    [Pg.401]    [Pg.171]    [Pg.367]    [Pg.28]    [Pg.270]    [Pg.417]    [Pg.459]    [Pg.160]    [Pg.131]    [Pg.505]    [Pg.547]    [Pg.548]    [Pg.395]    [Pg.530]    [Pg.195]    [Pg.41]    [Pg.419]    [Pg.496]    [Pg.510]    [Pg.532]    [Pg.533]    [Pg.251]    [Pg.310]    [Pg.274]    [Pg.448]    [Pg.45]    [Pg.47]    [Pg.49]    [Pg.322]    [Pg.415]    [Pg.598]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.19 , Pg.20 , Pg.22 , Pg.26 , Pg.50 , Pg.53 , Pg.87 , Pg.105 , Pg.106 , Pg.107 , Pg.109 , Pg.112 , Pg.117 , Pg.176 , Pg.180 , Pg.185 ]




SEARCH



Microscopic Measurement of Particle Size

Particle size determination scanning electron microscop

Particle size determination transmission electron microscop

Particle size measurement microscope methods

Particle size, measurement light microscope

Particle sizing with confocal microscope

© 2024 chempedia.info