Synthetic Versus Biological Networks, Volume 2, Volume 2B. T. Stokke, A. Elgsaeter The Wiley Polymer Networks Group Review Series Volume 2 Synthetic versus Biological Networks Edited by B. T. Stokke and A. Elgsaeter The Norwegian University of Science and Technology, Trondheim, Norway This, the second volume in the series, presents articles from the 14th Polymer Networks Group conference which took place in Norway in July 1998 The focus of the conference was 'Synthetic versus Biological Networks' with papers highlighting the different ideas emerging from investigations into synthetic polymer networks as opposed to, and in comparison with, polymer networks of biological origins. The papers published in this volume have been divided into six sections: Network Formation Network Characterization Polymer Networks and Precursor Architectures Biopolymer Networks and Gels Biomedical Applications of Polymer Networks Polymer Networks in Restricted Geometries |
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Page 22
... cyclization parameter . The rate constants are in all cases the same ( functional groups reacting at random , without substitution effect ) . In the system without cyclization ( λ = 0 ) , the average size of molecules tend to zero soon ...
... cyclization parameter . The rate constants are in all cases the same ( functional groups reacting at random , without substitution effect ) . In the system without cyclization ( λ = 0 ) , the average size of molecules tend to zero soon ...
Page 27
... cyclization reactions which occur during free radical photopolymeriza- tions of multifunctional vinyl monomers are difficult to characterize because of the varying pendant double bond reactivities and inhomogeneities in the system . To ...
... cyclization reactions which occur during free radical photopolymeriza- tions of multifunctional vinyl monomers are difficult to characterize because of the varying pendant double bond reactivities and inhomogeneities in the system . To ...
Page 37
... cyclization is approxi- mately 35 % until 80 % monomer conversion . At the end of the reaction ( above 80 % monomer conversion ) the consumption of pendants increases relative to the consumption of pendants because the pendant ...
... cyclization is approxi- mately 35 % until 80 % monomer conversion . At the end of the reaction ( above 80 % monomer conversion ) the consumption of pendants increases relative to the consumption of pendants because the pendant ...
Contents
80 | 6 |
CONCLUSION | 12 |
Modelling of Network Polymerization with Intramolecular | 15 |
Copyright | |
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1999 John Wiley amphiphilic APCNs B.T. Stokke behavior birefringence blends calculated Chem chemical concentration conetworks copolymers counter ions critical conversion cross-polymerization crosslinking curing curves cyclization decrease deformation dendrimers dependence diacetylene diacetylene-containing diffusion diol distribution double bond dynamic light scattering Edited by B.T. effect Eichinger elastic Elgsaeter end-groups equation experimental formation formed functional groups gel point gelation Group Review Series hydrogel hydrophilic hyperbranched increase inhomogeneities isocyanate kinetic light scattering linear loop structures Macromolecules macromonomer materials measurements method modulus molecular weight molecules monomer Networks Group Review NIPAAm osmotic parameters particles pendant double bond phase separation Phys PNIPA poly(ethylene glycol polyelectrolyte polyester Polymer Networks Group polymerization polyurethane prepared properties QSPR radical ratio react reactivity Review Series Vol Sakyo-ku sample shear rate shown in Figure solution solvent swollen synthesis temperature transition values viscoelastic viscosity weight fraction Wiley Polymer Networks