4.6 Article

Thermal and Mechanical Properties of Esterified Lignin in Various Polymer Blends

Journal

MOLECULES
Volume 26, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26113219

Keywords

Kraft lignin; biopolymer; bioplastics

Funding

  1. Swedish Energy Agency

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The study successfully prepared lignin esters by modifying lignin with fatty acids, and incorporated them into different thermoplastic polymers to improve dispersibility while maintaining tensile properties. The results demonstrate significant impacts of lignin esters on the thermal and mechanical behavior of the blends.
Lignin is an abundant polymeric renewable material and thus a promising candidate for incorporation in various commercial thermoplastic polymers. One challenge is to increase the dispersibility of amphiphilic lignin in lipophilic thermoplastic polymers We altered Kraft lignin using widely available and renewable fatty acids, such as oleic acid, yielding more than 8 kg of lignin ester as a light brown powder. SEC showed a molecular weight of 5.8 kDa with a PDI = 3.80, while the T-g of the lignin ester was concluded to 70 degrees C. Furthermore, the lignin ester was incorporated (20%) into PLA, HDPE, and PP to establish the thermal and mechanical behavior of the blends. DSC and rheological measurements suggest that the lignin ester blends consist of a phase-separated system. The results demonstrate how esterification of lignin allows dispersion in all the evaluated thermoplastic polymers maintaining, to a large extent, the tensile properties of the original material. The impact strength of HDPE and PLA blends show substantial loss upon the addition of the lignin ester. Reconverting the acetic acid side stream into acetic anhydride and reusing the catalyst, the presented methodology can be scaled up to produce a lignin-based substitute to fossil materials.

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