Coloured random graphs explain the structure and dynamics of cross-linked polymer networks

被引:7
作者
Schamboeck, Verena [1 ]
Iedema, Piet D. [1 ]
Kryven, Ivan [2 ,3 ]
机构
[1] Univ Amsterdam, Vant Hoff Inst Mol Sci, Sci Pk 904, NL-1098 XH Amsterdam, Netherlands
[2] Univ Utrecht, Math Inst, POB 80010, NL-3508 TA Utrecht, Netherlands
[3] Ctr Complex Syst Studies, NL-3584 CE Utrecht, Netherlands
关键词
GEL REGIME; LINKING; KINETICS; TRANSITION; GELATION;
D O I
10.1038/s41598-020-71417-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Step-growth and chain-growth are two major families of chemical reactions that result in polymer networks with drastically different physical properties, often referred to as hyper-branched and cross-linked networks. In contrast to step-growth polymerisation, chain-growth forms networks that are history-dependent. Such networks are defined not just by the degree distribution, but also by their entire formation history, which entails a modelling and conceptual challenges. We show that the structure of chain-growth polymer networks corresponds to an edge-coloured random graph with a defined multivariate degree distribution, where the colour labels represent the formation times of chemical bonds. The theory quantifies and explains the gelation in free-radical polymerisation of cross-linked polymers and predicts conditions when history dependance has the most significant effect on the global properties of a polymer network. As such, the edge colouring is identified as the key driver behind the difference in the physical properties of step-growth and chain-growth networks. We expect that this findings will stimulate usage of network science tools for discovery and design of cross-linked polymers.
引用
收藏
页数:18
相关论文
共 43 条
[1]   Relative contributions of chain density and topology to the elasticity of two-dimensional polymer networks [J].
Alame, Ghadeer ;
Brassart, Laurence .
SOFT MATTER, 2019, 15 (28) :5703-5713
[2]  
[Anonymous], 2019, NATURE COMMUN, DOI DOI 10.1038/s41467-018-07882-8
[3]   Volumetric Bioprinting of Complex Living-Tissue Constructs within Seconds [J].
Bernal, Paulina Nunez ;
Delrot, Paul ;
Loterie, Damien ;
Li, Yang ;
Malda, Jos ;
Moser, Christophe ;
Levato, Riccardo .
ADVANCED MATERIALS, 2019, 31 (42)
[4]   Percolation on branching simplicial and cell complexes and its relation to interdependent percolation [J].
Bianconi, Ginestra ;
Kryven, Ivan ;
Ziff, Robert M. .
PHYSICAL REVIEW E, 2019, 100 (06)
[5]   Langevin approach for the dynamics of the contact process on annealed scale-free networks [J].
Boguna, Marian ;
Castellano, Claudio ;
Pastor-Satorras, Romualdo .
PHYSICAL REVIEW E, 2009, 79 (03)
[6]   Prediction of sol fraction and average molecular weights after gelation for non-linear free radical polymerizations using a kinetic approach [J].
Costa, MRPFN ;
Dias, RCS .
MACROMOLECULAR THEORY AND SIMULATIONS, 2003, 12 (08) :560-572
[7]   Rapid, continuous additive manufacturing by volumetric polymerization inhibition patterning [J].
de Beer, Martin P. ;
van der Laan, Harry L. ;
Cole, Megan A. ;
Whelan, Riley J. ;
Burns, Mark A. ;
Scott, Timothy F. .
SCIENCE ADVANCES, 2019, 5 (01)
[8]  
Dotson N.A., 1995, POLYM PROCESS MODELI
[9]   Constitution of three-dimensional polymers and the theory of gelation [J].
Flory, PJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1942, 46 (01) :132-140
[10]  
George O., 2004, PRINCIPLES POLYM, V4th