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Catalyst beads interface

Substrate-catalyst interaction is also essential for micellar catalysis, the principles of which have long been established and consistently described in detail [63-66]. The main feature of micellar catalysis is the ability of reacting species to concentrate inside micelles, which leads to a considerable acceleration of the reaction. The same principle may apply for polymer systems. An interesting way to concentrate the substrate inside polymer catalysts is the use of cross-linked amphiphilic polymer latexes [67-69]. Liu et al. [67] synthesized a histidine-containing resin which was active in hydrolysis of p-nitrophenyl acetate (NPA). The kinetics curve of NPA decomposition in the presence of the resin was of Michaelis-Menten type, indicating that the catalytic act was accompanied by sorption of the substrate. However, no discussion of the possible sorption mechanisms (i.e., sorption by the interfaces or by the core of the resin beads) was presented. [Pg.196]


See other pages where Catalyst beads interface is mentioned: [Pg.287]    [Pg.212]    [Pg.8]    [Pg.68]    [Pg.95]    [Pg.127]    [Pg.5]    [Pg.160]    [Pg.5]    [Pg.614]    [Pg.27]    [Pg.189]    [Pg.719]    [Pg.486]    [Pg.43]    [Pg.877]    [Pg.193]    [Pg.200]    [Pg.57]   
See also in sourсe #XX -- [ Pg.7 ]




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Catalyst beads

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