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Microspheres particles

Two-phase suspension systems produce beaded products with broader particle-size distribution (e.g., 1-50 /rm). The microspherical particles usually need to be classified repeatedly to reduce the particle-size distribution in order to improve the resolution and efficiency in the separation for use in chromatography. The actual classification process depends on the size range involved, the nature of the beaded product, and its intended applications. Relatively large (>50 /rm) and mechanically stable particles can be sieved easily in the dry state, whereas small particles are processed more conveniently in the wet state. For very fine particles (<20 /rm), classification is accomplished by wet sedimentation, countflow setting, countflow centrifugation, or air classification. [Pg.6]

Inada et al. succeeded in combining an enzyme with synthesized magnetic particles, which made reuse of enzymes easy (61). Furthermore, magnetic polymeric microsphere particles are employed for labeling and separation of biocells (62). Recently many magnetic particles modified with specific proteins have been employed for extraction and cleaning of DNA (63). [Pg.675]

Microsphere volnme fraction is 0.60 b> Values calculated using microsphere particle density of 237 kg/m3 and resin density of 1400 kg/m3... [Pg.82]

Inada et al. succeeded in combining enzyme on synthesized magnetic particles. Thermosensitive magnetic particles that are useful for separation of enzyme and biomaterials have been reported. Furthermore, since magnetic polymeric microsphere particles were developed for labeling and separation of biocells, " studies into the applications of magnetic particles in the biology and medical fields are under way. ... [Pg.695]

Microspherical particles of MCM-41 have been synthesized.1284 All the properties of the spherical MCM-41 particles are essentially the same as those of the MCM-41 materials synthesized by well established methods. [Pg.579]

Figure 3. Microfluidic Device. (A) Time lapse illustrating repulsion the ejection of 1.9 pm fluorescent polystyrene microsphere particles from an electroactive microwell. After dissolution of the membrane, the fluorescent particles can be seen in the well. White hnes outline the gold electrodes features. Images are taken every 2 s (total of 10 s). (B) Schematic of the electroactive microwell drug delivery system developed here. Scale bar represents 2 mm. (C) Micro fluidic device with electrical leads connected to thin copper wires. Inset Magnified view of microchip from above looking at the region near the membrane. (D) To illustrate the electrokinetic transport processes involved in the ejection stage, a finite element analysis of time-dependent species transport of the system is shown. Images show cut view of species concentration every 60 s up to 300 s after the ejection process. Figure 3. Microfluidic Device. (A) Time lapse illustrating repulsion the ejection of 1.9 pm fluorescent polystyrene microsphere particles from an electroactive microwell. After dissolution of the membrane, the fluorescent particles can be seen in the well. White hnes outline the gold electrodes features. Images are taken every 2 s (total of 10 s). (B) Schematic of the electroactive microwell drug delivery system developed here. Scale bar represents 2 mm. (C) Micro fluidic device with electrical leads connected to thin copper wires. Inset Magnified view of microchip from above looking at the region near the membrane. (D) To illustrate the electrokinetic transport processes involved in the ejection stage, a finite element analysis of time-dependent species transport of the system is shown. Images show cut view of species concentration every 60 s up to 300 s after the ejection process.
FI9. 31.6. (a) Zorbax porous silica microsphere particle, 50% porosity, 100-A pores, (b) Xerogel silica particle, 70% porosity, 100-A pores. (Courtesy of Agilent Technologies.)... [Pg.608]

Rigidity and mechanical stability of the substrate under conditions of high-performance liquid chromatography are important and microspherical particles of macroporous highly crosslinked PS-DVB or poly(metacrylate) and silica are well suited for CIC. There are three main methods of producing a chelating ion-exchange surface. [Pg.2309]

Applications abrasive products, adhesives, binder, electrodes, membranes, microspheres, particle boards, thermal Insulation ... [Pg.409]

One of the fascinating application of macromonomers is in the field of dispersion polymerization. The dispersion polymerization in the presence of suitable stabilizers affords mostly monodisperse submicron- and micron-sized microspheres (particles). The macromonomers are graft-copolymerizaed during copolymerization in the continuous phase and so accumulate on the particle surface, so that the resulting particles are effectively sterically stabilized against flocculation. Amphiphilic copolymers s mthesized by copolymerization of a hydrophobic conventional monomer with a hydrophilic macromonomer and vice verse present all the typical properties of conventional surfactants. They aggregate between themselves and form a micelle in the aqueous or non-aqueous media. The conformation of a micelle formed by PEO-g-PSt polymer in the aqueous medium consists of a hydrophobic PSt core and a hydrophilic PEO shell (Fig. 10). [Pg.107]

Liu and co-workers prepared high-flux microflltration Alters made of PVA electrospun nanoflbers [25]. The Alters were fabricated by electrospinning of PVA onto a nonwoven support and followed by chemical cross-linking with glutaraldehyde in acetone. Due to the high porosity and hydrophilicity, the Alters outperformed Millipore GSWP 0.22-p,m Alters with 3-7 times pure water flux and had an ability to reject 98 % of 0.2-p,m-sized polycarboxylate microsphere particles. The PVA ENMs should be a good candidate as microflltration Alters for water purification. [Pg.339]

Figure 22 Schematic representation of the situation at the contact line where microsphere particles segregate at different positions. Reprinted with permission from Perelaer, J. Smith, P. J. Hendriks, C. E. etal. Soft Matter2006,4,1072. Copyright 2010 the Royal Society of Chemistry. Figure 22 Schematic representation of the situation at the contact line where microsphere particles segregate at different positions. Reprinted with permission from Perelaer, J. Smith, P. J. Hendriks, C. E. etal. Soft Matter2006,4,1072. Copyright 2010 the Royal Society of Chemistry.

See other pages where Microspheres particles is mentioned: [Pg.209]    [Pg.34]    [Pg.3590]    [Pg.363]    [Pg.428]    [Pg.49]    [Pg.382]    [Pg.439]    [Pg.264]    [Pg.981]    [Pg.1000]    [Pg.1001]    [Pg.1002]    [Pg.1004]    [Pg.199]    [Pg.371]    [Pg.139]    [Pg.143]    [Pg.143]    [Pg.164]    [Pg.165]   
See also in sourсe #XX -- [ Pg.139 , Pg.143 , Pg.150 , Pg.165 ]




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