Pore size scanning electron

Fig. 18. Cross-sectional scanning electron micrograph of a three-layered alumina membrane/support (pore sizes 0.2, 0.8, and 12 p.m, respectively).

Figure 20 A typical scanning electron micrograph of the macroporous uniform poly(styrene-divinylbenzene) late> particles. Magnification 1200 x, (particle size = 16.0/rm average pore diameter = 200 nm).

Nitrogen adsorption isotherms were measured with a sorbtometer Micromeretics Asap 2010 after water desorption at 130°C. The distribution of pore radius was obtained from the adsorption isotherms by the density functional theory. Electron microscopy study was carried out with a scanning electron microscope (SEM) HitachiS800, to image the texture of the fibers and with a transmission electron microscope (TEM) JEOL 2010 to detect and measure metal particle size. The distribution of particles inside the carbon fibers was determined from TEM views taken through ultramicrotome sections across the carbon fiber. 

Scanning electron microscopy and other experimental methods indicate that the void spaces in a typical catalyst particle are not uniform in size, shape, or length. Moreover, they are often highly interconnected. Because of the complexities of most common pore structures, detailed mathematical descriptions of the void structure are not available. Moreover, because of other uncertainties involved in the design of catalytic reactors, the use of elaborate quantitative models of catalyst pore structures is not warranted. What is required, however, is a model that allows one to take into account the rates of diffusion of reactant and product species through the void spaces. Many of the models in common use simulate the void regions as cylindrical pores for such models a knowledge of the distribution of pore radii and the volumes associated therewith is required. 

For efficient separation, porous inorganic membranes need to be crack-free and uniform in pore size. An important reason for the increasing acceptance of ceramic membranes introduced in recent years is the consistent quality as exemplified in a scanning electron micrograph of the surface of a 0.2 micron pore diameter alumina membrane (Figure 3.3). 

Image analysis has been used to characterize the pore structure of synthetic membrane materials. The Celgard films have also been characterized by scanning tunneling microscopy, atomic force microscopy, and field emission scanning electron microscopy. The pore size of the Celgard membranes can also be calculated from eq 5, once the MacMullin number and gurley values are known. 

Fig. 4a, b. Scanning electron photomicrographs of amorphous poly(L-lactic acid) foams a 92% porosity and 30 pm median pore diameter b and 91% porosity and 94 pm median pore diameter. Prepared by a solvent-casting and particulate-leaching method [32] using 90 wt% sieved sodium chloride particles of size range between 0-53 pm and 106-150 pm, respectively... 

Fig. 7a, b. Scanning electron photomicrographs of PLLA foams of pore size 250-500 pm a cross-section at low magnification after 30 days of chondrocyte culture b and on the surface at high magnification after 28 days of chondrocyte culture (Reproduced with permission from [39])... 

For the detailed study of reaction-transport interactions in the porous catalytic layer, the spatially 3D model computer-reconstructed washcoat section can be employed (Koci et al., 2006, 2007a). The structure of porous catalyst support is controlled in the course of washcoat preparation on two levels (i) the level of macropores, influenced by mixing of wet supporting material particles with different sizes followed by specific thermal treatment and (ii) the level of meso-/ micropores, determined by the internal nanostructure of the used materials (e.g. alumina, zeolites) and sizes of noble metal crystallites. Information about the porous structure (pore size distribution, typical sizes of particles, etc.) on the micro- and nanoscale levels can be obtained from scanning electron microscopy (SEM), transmission electron microscopy ( ), or other high-resolution imaging techniques in combination with mercury porosimetry and BET adsorption isotherm data. This information can be used in computer reconstruction of porous catalytic medium. In the reconstructed catalyst, transport (diffusion, permeation, heat conduction) and combined reaction-transport processes can be simulated on detailed level (Kosek et al., 2005). 

Figure 25-5 Scanning electron micrographs of silica chromatography particles, (a) Aggregate of spherical particles with 50% porosity and a surface area of 150 m2/g. (b) Spongelike structure with 70% porosity and a surface area of 300 m2/g. Pores are the entryways into the interior of the particles. In both cases, the nominal pore size is 10 nm, but the distribution of pore sizes is greater in the spongelike structure. The spongelike structure also dissolves more readily in base. [From Hewlett-Packard Co. and R. Majors, LCGC May 1997, p. S8.J...

Powdered, particulate MCM-41 molecular sieves (Si/Al = 37) with varied pore diameters (1.80, 2.18, 2.54 and 3.04 nm) were synthesized following the conventional procedure using sodium silicate, sodium aluminate and C TMAB (n = 12, 14, 16 and 18) as the source materials for Si, A1 and quaternary ammonium surfactants, respectively [13]. Each sample was subjected to calcination in air at 560 °C for 6 h to remove the organic templates. The structure of the synthesized material was confirmed by powder X-ray diffraction (XRD) and by scanning/transmission electron microscopy. Their average pore sizes were deduced from the adsorption curve of the N2 adsorption-desorption isotherm obtained at 77 K by means of the BJH method (Table 1). 

The new composite (SC-155) and some of its precursors and derivatives were characterized by LOI (loss on ignition), XRD ( X ray diffraction), 1R (infrared spectra), BET specific surface area, nitrogen adsorption desorption isotherms, pore size distribution (mercury porosimetry), dynamic methylene blue adsorption and SEM (Scanning Electron... 

---