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Particle size analysis distribution types

The final product was elastic and self-tacking white solid. Upon dissolution in THF and drying, the solid was ttanslucent, indicating a block copolymer structure. Particle size analysis of the latex is shown in Fig. 3.2.4 to have a multimodal distribution, ranging from submicron to 10 p,m or greater, but still a stable enough emulsion. In fact, all of our latex products made from this type of emulsion FRRPP... [Pg.194]

Particle size analysis and measurement is an important operation in many industries. The stability, chemical reactivity, opacity, flowability, material strength, and some other properties of many materials are affected by the size distribution and characteristics of the particles within them. There are numerous techniques and instrumentation for all types of particle size analysis and characterization available. Some primary properties of particulate materials, mainly shape, will determine the way the particles are detected or... [Pg.89]

Before a technique can be selected for particle size analysis, two important decisions have to be made about the variables we measure i.e. the measure of particle size x and the type of size distribution required. [Pg.31]

The results of the particle size analysis obtained from the SAXS are summarized in Table 6.1, which shows the sizes corresponding to the particle size distribution maxima, R (Figure 6.5), and the two types of mean radii those obtained from the distribution curves and those calculated using the Hosemann approach [52] and respectively. [Pg.233]

Although the symbol PSA stands for Particle Size Analysis, there has always been included in each PSA Conference a scientific session on surface area estimation. At PSA 91, two main thrusts were to be found one being on the measurement on porosity of powders in terms of meso- and micro-porosity [Sing Buczek Cowan and Wenman] and the other, because of the global need to have traceability and mandatory powder product specifications, on the characterisation and conparability of reference materials [Stanley-Wbod, Osborne and Till] and the need for Standards [Lines]. The particle size distributions reported by several types of measuring instruments for the same materials were presented [Jimbo, Tsubaki and Yamamoto],... [Pg.551]

The preceding sections have focused on the properties of distributions in general without considering any particular type of distribution. In this section, we describe the characteristics and applications of the lognormal distribution for aerosol particle size analysis. As discussed below, the normal distribution, although widely used elsewhere, is not suitable for most aerosol particle size distributions. [Pg.47]

However, in most cases the AW(D) dependencies are distinctly nonlinear (Fig. 9), which gives impulse to further speculations. Clearly, dependencies of this type can result only from mutual suppression of the hydrogel particles because of their nonuniform distribution over the pores as well as from the presence of a distribution with respect to pore size which does not coincide with the size distribution of the SAH swollen particles. A considerable loss in swelling followed from the W(D) dependencies, as shown in Fig. 9, need a serious analysis which most probably would lead to the necessity of correlating the hydrogel particle sizes with those of the soil pores as well as choice of the technique of the SAH mixing with the soil. Attempts to create the appropriate mathematical model have failed, for they do not give adequate results. [Pg.129]

The extraction of more complex particle size distributions from PCS data (which is not part of the commonly performed particle size characterization of solid lipid nanoparticles) remains a challenging task, even though several corresponding mathematical models and software for commercial instruments are available. This type of analysis requires the user to have a high degree of experience and the data to have high statistical accuracy. In many cases, data obtained in routine measurements, as are often performed for particle size characterization, are not an adequate basis for a reliable particle size distribution analysis. [Pg.4]

Sieve analysis using standard mesh screens is commonly used to determine particle size and size distribution of pellets and the reader is referred to standard texts for further information (61). Several types of densities have been defined for pellets based on interparticulate (void fraction) and intraparticulate pore volumes and include true, apparent, effective, bulk and tapped. The bulk and tapped densities may be obtained using simple devices, such as that used to evaluate granulations in tableting, while the true and apparent densities need more complex techniques based on mercury intrusion, gas flow, powder displacement, imaging or minimum fluidization velocity (62). [Pg.353]

The analysis of the autocorrelation function data by the Coulter Model N4 is carried out by the Size Distribution Program (SDP), which gives the particle size distribution in the form of various output displays (see Section 10.4). The SDP analysis utilizes the computer program CONTIN developed by S.W. Provencher (ref. 467-470 see also Section 10.2). (This program has been tested on computer-generated data, monomodal polystyrene samples, and a vesicle system (ref. 466-468,471).) Since the SDP does not fit to any specific distribution type, it offers the ability to detect multimodal and very broad distributions. [Pg.163]

Species distribution studies have shown that trace element (e.g. metals) concentrations in soils and sediments vary with physical location (e.g. depth below bed surface) and with particle size. In these speciation studies the total element content of each fraction was determined using a suitable trace element procedure, for example, solid sample analysis by X-ray emission spectroscopy or neutron activation analysis, or alternatively by dissolution of sample and analysis by ICPOES, AAS or ASV. The type of sample fraction analysed can vary, and a few... [Pg.13]

The results reported herein indicate that hydrodynamic chromatography is an accurate, reproducible technique for latex particle size distribution analysis. Typical analysis requires 15-20 minutes to complete and reproducibility is generally better than 5% for both reported particle size and mass percent. Latex particle size distributions found using HDC provide useful information about end use performance of many types of material (see Table V). [Pg.268]

Hatch extended his method of analysis to size-distribution curves ranging from coarse-screen analysis through fine particles measured microscopically. While excellent results were obtained by using this technique on laboratory samples, the method cannot be generalized to cover all types of distributions encountered in practice. As already explained in Chapter 3, size-frequency distributions may assume a variety of shapes. The Hatch development applies only to distributions which follow the normal or log-probability law. When size-distributions are hyperbolic in the lower extremes and follow normal log-probability laws in the upper extremes, the Hatch analysis must necessarily fail. Nevertheless, the relationships developed by Hatch have a far-reaching practical importance... [Pg.118]


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