Contribution of Entanglements to Polymer Network Elasticity

被引:45
作者
Campise, F. [1 ]
Agudelo, D. C. [2 ]
Acosta, R. H. [1 ]
Villar, M. A. [2 ]
Valles, E. M. [2 ]
Monti, G. A. [1 ]
Vega, D. A. [3 ]
机构
[1] Univ Nacl Cordoba, FAMAF, CONICET, IFEG, Cordoba, Argentina
[2] Univ Nacl Sur, CONICET, Planta Piloto Ingn Quim, Deparment Chem Engn, Bahia Blanca, Buenos Aires, Argentina
[3] Univ Nacl Sur, CONICET, Inst Fis Sur IFISUR, Dept Phys, Bahia Blanca, Buenos Aires, Argentina
关键词
MODEL POLY(DIMETHYLSILOXANE) NETWORKS; CROSS-LINK DENSITY; RUBBER ELASTICITY; PENDANT CHAINS; VISCOELASTIC PROPERTIES; TRAPPED ENTANGLEMENTS; MECHANICAL-PROPERTIES; DYNAMICS; DEFECTS; MELTS;
D O I
10.1021/acs.macromol.6b02784
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Trapped entanglements, cross-linker functionality, and elastically effective chains are the sources of elasticity of polymer networks and gels. However, despite more than 80 years of theoretical and experimental research in this field, still little is known about their relative contribution to network elasticity. In this work, we use double quantum nuclear magnetic resonance (DQNMR) experiments to characterize the elasticity of model polymer networks prepared with cross-linkers of mixed functionality and control of structural defects. An order parameter that condensates the elastic response within the theoretical framework of the entangled phantom theory for rubber elasticity was identified. Standard lore dictates that low molecular weight precursors for the elastically active chains leads to a negligible contribution of trapped entanglements. Here we show that the contribution of trapped entanglements may equal the contribution coming from elastically active material and that it is independent of network topology.
引用
收藏
页码:2964 / 2972
页数:9
相关论文
共 39 条
[1]   Transiently Trapped Entanglements in Model Polymer Networks [J].
Acosta, Rodolfo H. ;
Monti, Gustavo A. ;
Villar, Marcelo A. ;
Valles, Enrique M. ;
Vega, Daniel A. .
MACROMOLECULES, 2009, 42 (13) :4674-4680
[2]   ELASTICITY OF ENTANGLED NETWORKS [J].
BALL, RC ;
DOI, M ;
EDWARDS, SF ;
WARNER, M .
POLYMER, 1981, 22 (08) :1010-1018
[3]   NMR-STUDIES OF CLUSTERING IN SOLIDS [J].
BAUM, J ;
PINES, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (24) :7447-7454
[4]   Contribution of Linear Guest and Structural Pendant Chains to Relaxational Dynamics in Model Polymer Networks Probed by Time-Domain 1H NMR [J].
Campise, F. ;
Roth, L. E. ;
Acosta, R. H. ;
Villiar, M. A. ;
Valles, E. M. ;
Monti, G. A. ;
Vega, D. A. .
MACROMOLECULES, 2016, 49 (01) :387-394
[5]   Cross-Link Density Estimation of PDMS Networks with Precise Consideration of Networks Defects (vol 45, pg 899, 2012) [J].
Chasse, Walter ;
Lang, Michael ;
Sommer, Jens-Uwe ;
Saalwaechter, Kay .
MACROMOLECULES, 2015, 48 (04) :1267-1268
[6]   Thermodynamics of Swollen Networks As Reflected in Segmental Orientation Correlations [J].
Chasse, Walter ;
Saalwaechter, Kay ;
Sommer, Jens-Uwe .
MACROMOLECULES, 2012, 45 (13) :5513-5523
[7]   Cross-Link Density Estimation of PDMS Networks with Precise Consideration of Networks Defects [J].
Chasse, Walter ;
Lang, Michael ;
Sommer, Jens-Uwe ;
Saalwaechter, Kay .
MACROMOLECULES, 2012, 45 (02) :899-912
[8]   Time-Domain NMR Observation of Entangled Polymer Dynamics: Analytical Theory of Signal Functions [J].
Chavez, Fabian Vaca ;
Saalwaechter, Kay .
MACROMOLECULES, 2011, 44 (06) :1560-1569
[9]  
DOI M, 1980, J POLYM SCI POL LETT, V18, P775, DOI 10.1002/pol.1980.130181205
[10]   THE TUBE MODEL-THEORY OF RUBBER ELASTICITY [J].
EDWARDS, SF ;
VILGIS, TA .
REPORTS ON PROGRESS IN PHYSICS, 1988, 51 (02) :243-297