Chemical and Rheological Characteristics of Thermally Stable Kraft Lignin Polycondensates Analyzed by Dielectric Properties
- Authors
- Le Dai Duong; Nguyen Dang Luong; Nguyen Thi Thanh Binh; Park, In Kyung; Lee, Seong Hoon; Kim, Dea Sik; Lee, Yong Sang; Lee, Young Kwan; Kim, Byung Woo; Kim, Kwang Ho; KyuYoon, Ho; Yun, Ju Ho; Do Nam, Jae
- Issue Date
- 2013
- Publisher
- NORTH CAROLINA STATE UNIV DEPT WOOD & PAPER SCI
- Keywords
- Lignin; Polycondensate; Polycaprolactone; Biodegradable polymer; Eco-friendly
- Citation
- BIORESOURCES, v.8, no.3, pp.4518 - 4532
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIORESOURCES
- Volume
- 8
- Number
- 3
- Start Page
- 4518
- End Page
- 4532
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/106445
- ISSN
- 1930-2126
- Abstract
- In light of the difficulties and disagreements in determining the property-processing structure relations of lignin-based polymers, dielectric analysis was used to identify the thermal and rheological characteristics of a lignin-based polycondensate and the pristine lignin. Using dielectric analysis, the pristine lignin with M-w=6000 g/mol, was clearly identified as giving the wet glass transition temperature (T-g,T-wet) and the evolution of gases (i.e., burning) at around 80 degrees C to 125 degrees C followed by subsequent cross-linking reactions over 150 degrees C to give the dry glass transition temperature (T-g,T-dry) of lignin at around 130 degrees C to 140 degrees C. Connecting the lignin macromers using sequential condensation reactions with caprolactone and sebacoyl chloride, the lignin based polycaprolactone (LigPCL) polycondensates were synthesized as a thermoplastic polymer composed of lignin macromers and aliphatic polyester chains with M-w=10500 g/mol. The synthesized LigPCL presented good thermal stability and rheological melting behavior without evolving odor or fumes. In particular, the T-2% (defined at 2% of weight loss) of the LigPCL and pristine lignin were 200 degrees C and 80 degrees C, respectively. The melt viscosity was measured at 10(3)Pa.s at 120 degrees C, ensuring facile melt-blending processing with various commodity polymers to be used in eco-friendly polymer composite development.
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