Effect of the molecular weight between crosslinks of thermally cured epoxy resins on the CO2‐bubble nucleation in a batch physical foaming process. Issue 12 (27th January 2014)

• Record Type: Journal Article
• Authors: Ito, Akihiro; Semba, Takeshi; Taki, Kentaro; Ohshima, Masahiro
• Is Part Of: Journal of applied polymer science. Volume 131:Issue 12(2014:Jun. 15)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2014-01-27
• Subjects: Polymers -- Periodicals; Polymerization -- Periodicals; 668.9
• DOI: 10.1002/app.40407
• Languages: English
• ISSNs: 0021-8995

Abstract

<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Epoxy resins (bisphenol A type epoxy resins/2‐ethyl‐4‐methylimidazole) consisting of oligomers with different molecular weights were foamed using a temperature‐quench physical foaming method with CO<sub>2</sub>. The resulting cell morphologies could be classified into four types: non‐foamed structure, cracked structure, star‐shaped structure, and sphere‐shaped structure. The effects of the gel fraction and molecular weight between crosslinks (<italic>M<sub>C</sub></italic>) on the cell morphology were investigated for the preparation of microcellular epoxy foams. <italic>M<sub>C</sub></italic> was calculated by measuring the plateau rubber modulus of the rheological properties and the weight uptake of acetone. By varying the molecular weight of the epoxy oligomers and the cure time, the <italic>M<sub>C</sub></italic> of the epoxy was controlled to modulate the cell morphology. The experiments elucidated the threshold <italic>M<sub>C</sub></italic> value that permits CO<sub>2</sub>‐bubble nucleation: CO<sub>2</sub>‐bubble nucleation in the epoxy resin could be induced when the distance between the crosslinking points exceeded the critical size of bubble nucleus. Based on this information, the microcellular epoxy foam was prepared by maintaining M<sub>C</sub> above 10<sup>4</sup>g mol<sup>−1</sup> and the complex modulus above 6 × 10<sup>8</sup> Pa. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. <bold>2014</bold>, <italic>131</italic>, 40407.</p> </abstract>