Virtual Synthesis of Thermally Cross-Linked Copolymers from a Novel Implementation of Polymatic

被引:32
作者
Abbott, Lauren J. [1 ]
Hughes, Justin E. [1 ]
Colina, Coray M. [1 ]
机构
[1] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
基金
美国国家科学基金会;
关键词
HIGH-SURFACE-AREA; INTRINSIC MICROPOROSITY; MOLECULAR SIMULATIONS; CARBON-DIOXIDE; POLYMER; ADSORPTION; HYDROGEN; POLYSTYRENE; EQUILIBRIA; MEMBRANES;
D O I
10.1021/jp409664d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Because of the complex connectivity of cross-linked polymers, generating structures for molecular simulations is a nontrivial task. In this work, a general methodology is presented for constructing post-cross-linked polymers by a new two-stage implementation of the Polymatic simulated polymerization algorithm, where linear polymers are first polymerized and then cross-linked. It is illustrated here for an example system of thermally cross-linked octene-styrene-divinylbenzene (OS-DVB) copolymers. In the molecular models, the degree of cross-linking is ranged from 0 to 100%, and the resulting structural and thermal properties are examined. The simulations reveal an increase in the free volume with higher cross-linking degrees. Shifts in the peaks of the structure factors, which are assigned to contributions from the backbone and side-chain atoms, correspond to the formation of larger free volume elements. Furthermore, the glass transition temperatures increase with higher degrees of cross-linking, while the thermal expansivity decreases. Comparisons with experimental results for similar systems are made when available. As demonstrated here, the presented methodology will provide an effective route to simulating post-cross-linked polymers for a variety of applications, which will enable an improved understanding of their structure-property relationships.
引用
收藏
页码:1916 / 1924
页数:9
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