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Anionic Polymerization of Methylene Malonate for High-Performance Coatings AITranslate

University of Massachusetts Amherst; University of Massachusetts Amherst; University of Massachusetts Amherst; University of Massachusetts Amherst; University of Massachusetts Amherst
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Publisher: ACS
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Abstract AITranslate

Here, we demonstrate the anionic polymerization and the high reactivity of the novel monomer diethyl methylene malonate (DEMM). At room temperature and under atmospheric conditions, water and anionic functional groups (i.e., carboxyl, boronic, and phenol) quickly initiate DEMM. The polymerization of DEMM in water and the final molecular weight of the polymer were both demonstrated to be pH-dependent. Systematically, investigations were conducted to study the conversion rate of DEMM with various functional groups, and the polymerization was verified to occur with anionic groups using a carboxylate-initiated DEMM system. For coating applications, we also investigated a multifunctional derivative monomer called (DEMM)6 that is an oligomeric polyester of DEMM esterified with butanediol that contains on average six repeat units of reactive DEMM (commercially known as Forza B3000 XP). The incorporation of 15 wt % (DEMM)6 into latex containing methacrylate acid as a functional monomer yielded cross-linked coatings with a gel content of 76.25 wt % that had a 289% improvement in rub-resistance performance compared to controls (without (DEMM)6). This study provides a facile methodology to synthesize cross-linked latex coatings at room temperature.

KeyWords AITranslate

anionic polymerization methylene malonate reactivity initiation coatings polymerization
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.8b00135

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Citation Information:

Here, we demonstrate the anionic polymerization and the high reactivity of the novel monomer diethyl methylene malonate (DEMM). At room temperature and under atmospheric conditions, water and anionic functional groups (i.e., carboxyl, boronic, and phenol) quickly initiate DEMM. The polymerization of DEMM in water and the final molecular weight of the polymer were both demonstrated to be pH-dependent. Systematically, investigations were conducted to study the conversion rate of DEMM with various functional groups, and the polymerization was verified to occur with anionic groups using a carboxylate-initiated DEMM system. For coating applications, we also investigated a multifunctional derivative monomer called (DEMM)6 that is an oligomeric polyester of DEMM esterified with butanediol that contains on average six repeat units of reactive DEMM (commercially known as Forza B3000 XP). The incorporation of 15 wt % (DEMM)6 into latex containing methacrylate acid as a functional monomer yielded cross-linked coatings with a gel content of 76.25 wt % that had a 289% improvement in rub-resistance performance compared to controls (without (DEMM)6). This study provides a facile methodology to synthesize cross-linked latex coatings at room temperature.

quote

GB/T 7714-2015 [1] Mengfei Huang, Yuan Liu, Guozhen Yang, et al. ACS Applied Polymer Materials, 2019(1). DOI:10.1021/acsapm.8b00135.
MLA [1] Mengfei Huang, et al., ACS Applied Polymer Materials, no. 1, 2019, https://doi.org/10.1021/acsapm.8b00135.
APA [1] Mengfei Huang, Yuan Liu, Guozhen Yang, John Klier, & Jessica D. Schiffman. (2019). ACS Applied Polymer Materials(1). https://doi.org/10.1021/acsapm.8b00135
IEEE [1] Mengfei Huang, Yuan Liu, Guozhen Yang, John Klier, and Jessica D. Schiffman, ACS Applied Polymer Materials, no. 1, 2019, doi: 10.1021/acsapm.8b00135. keywords: {anionic polymerization;methylene malonate;reactivity;initiation;coatings;polymerization}