Counting Secondary Loops Is Required for Accurate Prediction of End-Linked Polymer Network Elasticity

被引:56
|
作者
Wang, Junpeng [1 ]
Lin, Tzyy-Shyang [2 ]
Gu, Yuwei [1 ]
Wang, Rui [2 ]
Olsen, Bradley D. [2 ]
Johnson, Jeremiah A. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
来源
ACS MACRO LETTERS | 2018年 / 7卷 / 02期
基金
美国国家科学基金会;
关键词
AZIDE-ALKYNE CYCLOADDITION; CLICK CHEMISTRY; PRIMARY CYCLIZATION; WATER-PURIFICATION; MOLECULAR DEFECTS; ADHESIVE POLYMERS; MODEL NETWORKS; CROSS-LINKING; HYDROGELS; GELS;
D O I
10.1021/acsmacrolett.8b00008
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
To predict and understand the properties of polymer networks, it is necessary to quantify network defects. Of the various possible network defects, loops are perhaps the most pervasive and yet difficult to directly measure. Network disassembly spectrometry (NDS) has previously enabled counting of the simplest loops primary loops but higher order loops, e.g., secondary loops, have remained elusive. Here, we report that the introduction of a nondegradable tracer within the NDS framework enables the primary and secondary loops in end-linked polymer networks for the first time. With this new "NDS2.0" method, the concentration dependences of the primary and secondary loop fractions are measured; the results agree well with a purely topological theory for network formation from phantom chains. In addition, semibatch monomer addition is shown to decrease both primary and secondary loops, though the latter to a much smaller extent. Finally, using the measured primary and secondary loop fractions, we were able to predict the shear storage modulus of end-linked polymer gels via real elastic network theory (RENT).
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页码:244 / 249
页数:11
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