4.7 Article

Bio-Based Polymer Developments from Tall Oil Fatty Acids by Exploiting Michael Addition

期刊

POLYMERS
卷 14, 期 19, 页码 -

出版社

MDPI
DOI: 10.3390/polym14194068

关键词

fatty acid-based Michael donor; Michael addition; bio-based polymer; tall oil

资金

  1. Latvian Council of Science [lzp-2020/1-0385]
  2. Riga Technical University's Doctoral Grant programme (DOK.OK) [TI/21]

向作者/读者索取更多资源

In this study, new polymer materials were obtained by using previously developed acetoacetates and different bio-based monomers. These polymers have comparable qualities to polyurethanes without the need for hazardous materials or reactions under harsh conditions.
In this study, previously developed acetoacetates of two tall-oil-based and two commercial polyols were used to obtain polymers by the Michael reaction. The development of polymer formulations with varying cross-link density was enabled by different bio-based monomers in combination with different acrylates-bisphenol A ethoxylate diacrylate, trimethylolpropane triacrylate, and pentaerythritol tetraacrylate. New polymer materials are based on the same polyols that are suitable for polyurethanes. The new polymers have qualities comparable to polyurethanes and are obtained without the drawbacks that come with polyurethane extractions, such as the use of hazardous isocyanates or reactions under harsh conditions in the case of non-isocyanate polyurethanes. Dynamic mechanical analysis, differential scanning calorimetry, thermal gravimetric analysis, and universal strength testing equipment were used to investigate the physical and thermal characteristics of the created polymers. Polymers with a wide range of thermal and mechanical properties were obtained (glass transition temperature from 21 to 63 degrees C; tensile modulus (Young's) from 8 MPa to 2710 MPa and tensile strength from 4 to 52 MPa). The synthesized polymers are thermally stable up to 300 degrees C. The suggested method may be used to make two-component polymer foams, coatings, resins, and composite matrices.

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