2008
DOI: 10.1002/masy.200850116
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Radical Homo‐ and Copolymerization of Acrylamide and Ionic Monomers in Weak Magnetic Field

Abstract: The synergy between magnetic field (MF) and electrostatic interactions on the kinetics of radical homopolymerization of acrylamide (AM), acrylic acid (AA), its ionized form acrylate (A À ) and diallyldimethylammonium chloride (DADMAC), as well as AM/AA, AM/A À , DADMAC/AA, and DADMAC/AM copolymerizations was investigated. The application of MF during the polymerizations significantly increased the monomer consumption rate (Rp) of all monomers in homo and copolymerizations and the molar masses of polyAA and pol… Show more

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Cited by 6 publications
(4 citation statements)
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“…As pointed out by the authors, k p was considered to be constant in their system because of the absence of radical–radical interaction; nevertheless, magnetic field induced molecular orientation that improved the k p could not be ruled out in other systems. In addition to previous work, efforts to the effect of magnetic field on the copolymerization of AM with ionic monomers (e.g., AA and DADMAC) have also been done by Rintoul et al , Results showed that the use of a magnetic field accelerated the monomer-consuming rate; however, the composition of the resulting copolymers did not respond to the external magnetic field. This resulted from the negligible difference in reactivity ratio calculated from the kinetic data obtained with and without applied magnetic field.…”
Section: Magneto-regulated Systemsmentioning
confidence: 99%
“…As pointed out by the authors, k p was considered to be constant in their system because of the absence of radical–radical interaction; nevertheless, magnetic field induced molecular orientation that improved the k p could not be ruled out in other systems. In addition to previous work, efforts to the effect of magnetic field on the copolymerization of AM with ionic monomers (e.g., AA and DADMAC) have also been done by Rintoul et al , Results showed that the use of a magnetic field accelerated the monomer-consuming rate; however, the composition of the resulting copolymers did not respond to the external magnetic field. This resulted from the negligible difference in reactivity ratio calculated from the kinetic data obtained with and without applied magnetic field.…”
Section: Magneto-regulated Systemsmentioning
confidence: 99%
“…Increase of molar mass of polyAA. No effect in the molar mass of polyAM and copolymer compositions [20,21] AA: acrylic acid, AC: vinyl acetate, AHC: 1,1 -azobis(cyclohexane-1-carbonitrile); AIBN: 2,2 -azobisisobutyronitrile; AM: acrylamide, AMP: 2,2 -azobis(2-methylpropionitrile); AN: acrylonitrile; APA: 4,4 -azobis(4-cyanopentanoic acid); BK: benzyl ketone; BMA: butylmethacrylate; BP: benzoyl peroxide, C 26 The aim of this work is to establish some criteria for recipe preparation and reaction conditions needed to study the MF effects on the kinetics of radical polymerization of acrylamide (AM) [22] and to conclude the consequences for the overall rate expression expressed as Equation (1) and the kinetic chain length expressed as Equation (2) [23]:…”
Section: An Aibn Bulkmentioning
confidence: 99%
“…Magnetite nanoparticles (MNPs) and gold nanoparticles (CNPs) have been tried as catalysts to enhance the GOx activity during the oxidation of glucose in blood samples [32][33][34][35]. Moreover, magnetic fields can accelerate organic reactions by interacting with unpaired electrons [36][37][38]. Carbon nanotubes (CNTs) were successfully used to bind GOx to the electrode substrates of several glucose skin sensors [20,[39][40][41][42]].…”
Section: Introductionmentioning
confidence: 99%