## Molecular basis of polymer networks: proceedings of the 5th IFF-Ill Workshop, Jülich, Fed. Rep. of Germany, October 5-7, 1988The contributors to this volume appraise our knowledge of the molecular physics of polymer networks and pinpoint areas of research where significant advances can be made using new theories and techniques. They describe both theoretical approaches, based on new theoretical concepts and original network models, and recent experimental investigations using SANS, 2H NMR or QELS. These new techniques provide precise information about network behaviour at the molecular level. Reported results of the application of these and more traditional techniques include the microscopic conformation and properties of permanent networks or gels formed by specific interchain interactions, the behaviour of elastomer liquid crystals, and the static and dynamic properties of star-branched polymers. |

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Page 128

... in the analysis we use here, one can write without loss of generality6,9 that w'(l

)=0 and then the results of equation (4) can be used to obtain the V-L function w'(

A) which appears in the term for the elastic contribution to the

...

... in the analysis we use here, one can write without loss of generality6,9 that w'(l

)=0 and then the results of equation (4) can be used to obtain the V-L function w'(

A) which appears in the term for the elastic contribution to the

**chemical potential**...

Page 148

THERMODYNAMICS OF NETWORKS The

component "i" is given by Hi = + ApVi + kbTfriai , (2) where fif is the standard

increase in ...

THERMODYNAMICS OF NETWORKS The

**chemical potential**of a non-networkcomponent "i" is given by Hi = + ApVi + kbTfriai , (2) where fif is the standard

**chemical potential**at an ambient pressure p and temperature T, Ap is theincrease in ...

Page 149

Changes in chemical potentials are not independent in a system in internal

equilibrium and the Gibbs-Duhem equation E ^jd/ij = 0 ... NETWORKS Material

components will tend to move if they are placed in gradients of their

Changes in chemical potentials are not independent in a system in internal

equilibrium and the Gibbs-Duhem equation E ^jd/ij = 0 ... NETWORKS Material

components will tend to move if they are placed in gradients of their

**chemical****potential**.### What people are saying - Write a review

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### Contents

Remarks | 2 |

The BaumgartnerMuthukumar Effect in Networks | 11 |

Statistical Mechanics of dDimensional Polymer Networks and Exact | 17 |

Copyright | |

13 other sections not shown

### Other editions - View all

Molecular Basis of Polymer Networks: Proceedings of the 5th IFF-ILL Workshop ... Artur Baumgärtner,Claude E. Picot No preview available - 2011 |

### Common terms and phrases

42 Molecular Basis anisotropy Basis of Polymer Bastide behaviour blends calculated carrageenan chain segments Chem chemical chemical potential configuration conformation constant constraints corresponding crosslinking curves deformation density dependence deswelling deuterated deviatoric distribution dynamics effect elastic free energy elementary strand elongation entanglements entropy equation equilibrium excluded volume experimental experiments exponent Flory Flory-Huggins Flory-Huggins theory fluctuations fractal dimension free chains free energy Gaussian gelation Gennes helix increases interaction parameter isotropic labelled paths layer length linear Macromolecules macroscopic measurements melt micronetworks modulus molecular weight monomers network chains neutron scattering observed obtained PDMS chains phantom network Phys polybutadiene polyelectrolyte Polymer Networks polymeric fractals polystyrene Proceedings in Physics properties radius of gyration ratio rod network Rouse model rubber elasticity S.F. Edwards sample scaling solution solvent Springer Proceedings star molecules star polymers swelling swollen temperature theory topological uniaxial values vector viscoelastic viscosity volume fraction