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Immobilization colloids

Deposition of Cold Nanoparticles and Clusters onto Carbons and Polymers 3.2.2.1 Cold Colloid Immobilization (Cl)... [Pg.59]

Figure 3.5 Schematic representation of colloid immobilization (Cl) method. Figure 3.5 Schematic representation of colloid immobilization (Cl) method.
Y. Xiao, H.X. Ju, and H.Y. Chen, Hydrogen peroxide sensor based on horseradish peroxidase-labeled Au colloids immobilized on gold electrode surface by cysteamine monolayer. Anal. Chim. Acta. 391,... [Pg.601]

Figure C 1.5.6. Single Ag nanoparticles imaged with evanescent-wave excitation. (A) Unfiltered photograph showing scattered laser light (514.5 nm) from Ag particles immobilized on a polylysine-coated surface. (B) Bandpass filtered (540-580 nm) photograph taken from a blank Ag colloid sample incubated witli 1 mM NaCl and... Figure C 1.5.6. Single Ag nanoparticles imaged with evanescent-wave excitation. (A) Unfiltered photograph showing scattered laser light (514.5 nm) from Ag particles immobilized on a polylysine-coated surface. (B) Bandpass filtered (540-580 nm) photograph taken from a blank Ag colloid sample incubated witli 1 mM NaCl and...
A unique feature of such DNA-directed self-assemblies is their site-selective immobilization, which makes it possible to construct well-defined nanostructures. On the other hand, the possibility of the introduction of a vast number of substitutes (like peptidic sequences, nucleoproteins, of hydrophobic hydrocarbon chains) to an adamantane core (adamantyl) makes such a process capable of designing steric colloidal and supramolecular conformations by setting hydrophobic/hydrophilic and other interactions. In addition, the rigidity of the adamantane structure can provide strength and rigidity to such self-assemblies [150]. [Pg.239]

Systems that contain the photocatalyst as a suspended powder or colloid are not convenient in continuous flow or circulation arrangements in which the photoactive system is held in place and can readily be removed for regeneration. CdS can be produced or immobilized in a Nafion membrane together with finely dispersed platinum... [Pg.136]

All soil metabolic proce.sses are driven by enzymes. The main sources of enzymes in soil are roots, animals, and microorganisms the last are considered to be the most important (49). Once enzymes are produced and excreted from microbial cells or from root cells, they face harsh conditions most may be rapidly decomposed by organisms (50), part may be adsorbed onto soil organomineral colloids and possibly protected against microbial degradation (51), and a minor portion may stand active in soil solution (52). The fraction of extracellular enzyme activity of soil, which is not denaturated and/or inactivated through interactions with soil fabric (51), is called naturally stabilized or immobilized. Moreover, it has been hypothesized that immobilized enzymes have a peculiar behavior, for they might not require cofactors for their catalysis. [Pg.171]

Thorium generally exists as a neutral hydroxide species in the oceans and is highly insoluble. Its behavior is dominated by a tendency to become incorporated in colloids and/or adhere to the surfaces of existing particles (Cochran 1992). Because ocean particles settle from the water column on the timescale of years, Th isotopes are removed rapidly and have an average residence time of = 20 years (Fig. 1). This insoluble behavior has led to the common assertion that Th is always immobile in aqueous conditions. While this is generally true in seawater, there are examples of Th being complexed as a carbonate (e.g.. Mono Lake waters, Anderson et al. 1982 Simpson et al. 1982) in which form it is soluble. [Pg.497]

Polymer-supported catalysts often have lower activities than the soluble catalysts because of the intraparticle diffusion resistance. In this case the immobilization of the complexes on colloidal polymers can increase the catalytic activity. Catalysts bound to polymer latexes were used in oxidation reactions, such as the Cu-catalyzed oxidation of ascorbic acid,12 the Co-catalyzed oxidation of tetralin,13 and the CoPc-catalyzed oxidation of butylphenol14 and thiols.1516 Mn(III)-porphyrin bound to colloidal anion exchange resin was... [Pg.248]

Olson LG, Lo YS, Beebe TP Jr, Harris JM (2001) Characterization of silane-modified immobilized gold colloids as a substrate for surface-enhanced Raman spectroscopy. Anal Chem 73 4268-4276... [Pg.165]

The first belief in the possibility of enzyme stabilization on a silica matrix was stated by Dickey in 1955, but he did not give experimental evidence, only mentioning that his experiments were unsuccessful [65]. A sol-gel procedure for enzyme immobilization in silica was first developed by Johnson and Whateley in 1971 [66]. The entrapped trypsin retained about 34 % of its tryptic activity observed in solution before the encapsulation. Furthermore, the enzyme was not released from the silica matrix by washing, demonstrating the increased stability and working pH range. Unfortunately, the article did not attract attention, although their method contained all the details that may be found in the present-day common approach. This was probably due to its publication in a colloid journal that was not read by biochemists. [Pg.82]

Layered materials are of special interest for bio-immobilization due to the accessibility of large internal and external surface areas, potential to confine biomolecules within regularly organized interlayer spaces, and processing of colloidal dispersions for the fabrication of protein-clay films for electrochemical catalysis [83-90], These studies indicate that layered materials can serve as efficient support matrices to maintain the native structure and function of the immobilized biomolecules. Current trends in the synthesis of functional biopolymer nano composites based on layered materials (specifically layered double hydroxides) have been discussed in excellent reviews by Ruiz-Hitzky [5] and Duan [6] herein we focus specifically on the fabrication of bio-inorganic lamellar nanocomposites based on the exfoliation and ordered restacking of aminopropyl-functionalized magnesium phyllosilicate (AMP) in the presence of various biomolecules [91]. [Pg.248]


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See also in sourсe #XX -- [ Pg.58 ]




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