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Composite beads

Fig. 8 Schematic representation of the so-called sacrificial silica approach to porous MIP beads and examples of SEM micrographs of the resulting beads (a) silica beads (b) composite beads (silica + MIP) (c) MIP beads after silica etching (d) ground bulk MIP employed as control. Reproduced with permission from [107]... Fig. 8 Schematic representation of the so-called sacrificial silica approach to porous MIP beads and examples of SEM micrographs of the resulting beads (a) silica beads (b) composite beads (silica + MIP) (c) MIP beads after silica etching (d) ground bulk MIP employed as control. Reproduced with permission from [107]...
Molecularly imprinted composite membranes have been developed based on the functionalisation of a commercial membrane with an MIP in order to improve the mechanical stability of the imprinted polymer phase, similarly to the preparation of MIP composite beads, discussed in Sect. 2.2.2. [Pg.73]

Table 8 and 9). In both instances the rates slacken as the matrix content is increased suggesting that the difTusion of ions through the matrix is the rate-determining step. For a fixed level and type of matrix, the adsorption rate increases with the decrease in the size of the composite bead (Table 10). The faster reaction of the smaller bead is the confirmation that the matrix is providing the main diffusion barrier. [Pg.103]

To prepare PAN-KCoFC and PAN-4A composite beads in which the inorganic powder content is 80 percent, the given amounts of inorganic powders were dispersed in DMSO(dimethylsulfuroxide) solvent and then mixed with PAN(polyacrylonitrile) polymer and a few c ops of TWEEN-80... [Pg.375]

The structural stability of the PAN-KCoFC and PAN-zeolite 4A composite beads in acid solution was proven by observing no weight loss for 3 day contact with the nitric acid solution of pH = 2. Also the results of ion exchange performance tests confirmed that the composite ion exchanger does not deteriorate by contacting with the acid solutions of pH = 2 for 3 days. [Pg.376]

Figure 1. Effect of air pressure on the PAN-KCoFC composite bead sizes, (a) Atmospheric pressure (b) 2 psi (c) 4 psi (d) 6 psi... Figure 1. Effect of air pressure on the PAN-KCoFC composite bead sizes, (a) Atmospheric pressure (b) 2 psi (c) 4 psi (d) 6 psi...
Matsunaga T, Maeda Y, Yoshino T et al (2007) FuUy automated immunoassay for detection of prostate-specific antigen using nano-magnetic beads and micro-polystyrene bead composites, Beads on Beads . Anal Chim Acta 597 331-339... [Pg.165]

Spherical beads possess better hydrodynamic and diffusion properties than irregularly shaped particles. It is, hence, desirable to apply MIPs in a spherical bead format, especially for flow-through applications. Methods to synthesize spherical polymer beads are often classified according to the initial state of the polymerization mixture (i) homogeneous (i.e. precipitation polymerization and dispersion polymerization) or (ii) heterogeneous (i.e. emulsion polymerization and suspension polymerization). In addition, several other techniques have been applied for the preparation of spherical MIP beads. The techniques of two-step swelling polymerization, core-shell polymerization, and synthesis of composite beads will be detailed here. [Pg.22]

The silica can be removed from a MIP-silica composite bead by dissolution with hydrofluoric acid, leaving a MIP bead that is a replica of the pore structure of the original silica bead [108, 109], MIP composites have also been made using, for example, chitosan as the support [110, 111],... [Pg.24]

Hasell T, Yang J, Wang W, Li J, Brown PD, Poliakoff M, Lester E, Howdle SM (2007) Preparation of polymer-nanoparticle composite beads by a nanoparticle-stabilised suspension polymerisation. J Mater Chem 17 4382-4386... [Pg.50]

No structure formation was observed by Vancaeyzeele et al. [54] after the encapsulation of unsymmetrical lanthanide-P-diketonato [lanthanide tris(4,4,4-trifluoro-1-(2-naphthyl-1,3-butanedione)] complexes (where the lanthanide is Pr, Ho, La, Tb, or Eu) in crosslinked PS nanoparticles. Single-element as well as multi-element particles of different sizes could be prepared. The lanthanide content of the particles was investigated using inductively coupled plasma mass spectrometry (ICP-MS) and optical emission spectrometry (ICP-OES) and determined as 1000 complexes per particle. By evaluating the lanthanide content in the continuous phase after removal of the particles, they found that no complex leaks from the composite beads. With exact determination of the element combination and their relative amounts, an elemental signature can be attributed to one specific particle batch. Exploiting this feature, Vancaeyzeele and coworkers could monitor the amount of internalization of differently sized element-encoded particles in different, clinically relevant cell lines. [Pg.195]

Figure 7 Molecular imprinting using porous silica beads as support. Scanning electron micrographs for (a) porous silica bead support (b) silica-MIP composite beads and (c) MIP beads after removal of the support. Figure 7 Molecular imprinting using porous silica beads as support. Scanning electron micrographs for (a) porous silica bead support (b) silica-MIP composite beads and (c) MIP beads after removal of the support.
The effects of % cofibre in composite beads and bead dosage on the Pb adsorption are shown in Figure 13.26. The data showed that the Pb ... [Pg.402]


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See also in sourсe #XX -- [ Pg.102 , Pg.103 ]

See also in sourсe #XX -- [ Pg.102 , Pg.103 ]




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