Particles size, determination

The specific surface estimated from particle size determined by electron microscopy was I lOm g . 

Besides phase identification XRD is also widely used for strain and particle size determination in thin films. Both produce peak broadenings, but they are distinguishable. Compared to TEM, XRD has poor area resolution capability, although by using synchrotron radiation beam diameters of a few pm can be obtained. Defect topography in epitaxial films can be determined at this resolution. 

Inhaled gaseous compounds are absorbed in all parts of the respiratory system whereas particle size determines how deep into the airways the parti cles will he transported in the airstrearn. Shortness of breath is a typical sign of a chemical exposure that has affected the lungs, and it may be evoked through iminunological mechanisms (e.g., formaldehyde, ethyleneoxide), or through toxic irritation (formaldehyde, isocyanates, sulfur dioxide, nitrogen dioxide, Frequently the mechanism depends on the concentration ol the com... 

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... 

The-results of the microscopic particle size determination are shown in Fig 22... 

H.L. Stalcup (Ref 28) evaluated the instru- -ment for the particle size determination of HMX used in rocket formulations. He found that Coulter Counter distribution was similar to that obtained with the Micromerograph except at the large particle end, where the Micromerograph indicated particles over lOOp compared to 32 p for the Coulter Counter. Median values were 13.5p by Micromerograph and 16 p for the Coulter Counter. The samples for the Coulter Counter were run on an as received basis, ie, while still water-isopropanol wet ... 

FIGURE 1 Effect of (sequential) extrusion of MLV dispersions through polycarbonate membrane filters (Unipore) with pore sizes of 1.0, 0.6, 0.4, 0.2, and 0.1 ym on the mean liposome diameter. DXR-containing MLV (phosphatidylcholine/phosphatidylserine/ cholesterol 10 1 4) mean diameter of nonextruded dispersion about 2 ym pH 4. Mean particle size determined by dynamic Light scattering (Nanosizer, Coulter Electronics). (From Crommelin and Storm, 1987.)... 

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. 

Because XPS is a surface sensitive technique, it recognizes how well particles are dispersed over a support. Figure 4.9 schematically shows two catalysts with the same quantity of supported particles but with different dispersions. When the particles are small, almost all atoms are at the surface, and the support is largely covered. In this case, XPS measures a high intensity Ip from the particles, but a relatively low intensity Is for the support. Consequently, the ratio Ip/Is is high. For poorly dispersed particles, Ip/Is is low. Thus, the XPS intensity ratio Ip/Is reflects the dispersion of a catalyst on the support. Several models have been reported that derive particle dispersions from XPS intensity ratios, frequently with success. Hence, XPS offers an alternative determination of dispersion for catalysts that are not accessible to investigation by the usual techniques used for particle size determination, such as electron microscopy and hydrogen chemisorption. 

Table III. Particle Size Determined Using Both MOssbauer...

The ideal packing should be relatively large in diameter, 80-100 nm, and be available with a pore size range from 500 to 10,000 A. The ores should be uniform in size distribution and shallow to reduce diffusion times. Improvements of this type will lead to the use of size exclusion chromatography for particle size determinations in the routine manner in which it is now employed for molecular weight determinations. 

The classical approach for particle size determination, or more correctly for particle size selection - which is still used for solids like soils, sediments and other technical materials like coal, and also for biological materials - is sieving analysis. The raw material is milled, generally after drying, see Section 2.1, and if the required particle size is obtained, typically ranging from <0.1 to a few mm, it is allowed to pass sieves with different apertures to discard coarse particles and remaining materials. For materials consisting of numerous different particles microscopical inspection is used. 

Fajgelj a and Zeisler R (1998) Particle size determination of some IAEA and NIST environmental and biological reference materials. Fresenius J Anal Chem 360 442-445. 

The methods by which particle size determination is carried out have been presented in Figure 2.3. The methods are observed to be broadly classified into two groups static meth-... 

The size of particles is of great importance, and particle size determinations should be carried out in preformulation as well in formulation functions. For small particle sizes, simple microscopy [41] may be used, but again imaging techniques, particularly with motorized stages, are more representative and much easier to carry out [42],... 

SM Milosovich. Particle-size determination via cascade impaction. Pharm Technol 16 82-86, 1992. 

WG Gorman, FA Carroll. Aerosol particle-size determination using laser holography. Pharm Technol 17 34-37, 1993. 

Particle shape plays an important role in particle size determination. The simplest definition of particle size diameter is based on a sphere, which has a unique diameter. In reality, however, many particles are not well represented by this model. Figure 1 illustrates the variety of shapes that may be found in particle samples [1]. As the size of a particle increases, so does its tendency to have an irregular shape [2], complicating statistical analysis. Particle shape coefficients have been derived for different geometries [3], and various equivalent diame-... 

With such a definition, it was found that vfc at 445 K did not change within experimental error as the average Pd particle size, determined by transmission electron microscopy (TEM), was varied between 1.5 and 8.0 nm (Figure 1). Besides, this value of v was also the same as that reported for the ill face of a single crystal of Pd (2), the latter value being itself very much the same on other planes of Pd or on a polycrystalline wire (3). 

In comparison with the neutralization methods previously described, lower sursat-urations are obtained with thermohydrolysis because the solubility of Pd(H20)2(0H)2 increases with temperature. Thermohydrolysis is then more favorable to particle growth. Figures 16a and b present the influence of temperature and the initial pH of the solution on the average PdO particle size determined by X-ray diffraction on the solid phase after precipitation. 

Steere, R. E., and G. K. Ackers Restricted diffusion chromatography through calibrated columns of granulated agar gel a simple method for particle-size determination. Nature /9d, 475 76 (1962). 

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