Chemical modification and plasma-induced grafting of pyrolitic lignin. Evaluation of the reinforcing effect on lignin/poly(l-lactide) composites

Pyrolitic lignin was modified through two methods. First, it was grafted with polylactide chains via a solvent-free process by ring-opening polymerization of l-lactide using calcium hydride as a catalyst. The efficiency of grafting was determined by infra-red, nuclear magnetic resonance and time-of-...

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Veröffentlicht in:Polymer (Guilford) 2017-06, Vol.118, p.280-296
Hauptverfasser: Atz Dick, Teo, Couve, Joël, Gimello, Olinda, Mas, André, Robin, Jean-Jacques
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Sprache:eng
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Zusammenfassung:Pyrolitic lignin was modified through two methods. First, it was grafted with polylactide chains via a solvent-free process by ring-opening polymerization of l-lactide using calcium hydride as a catalyst. The efficiency of grafting was determined by infra-red, nuclear magnetic resonance and time-of-flight secondary ion mass spectrometry analyses. Then, lignin particles were oxygen plasma-treated and immersed in l-lactide solution. Infra-red and X-ray photoelectron spectroscopy revealed that chains bearing ester groups similar to that of lactide were covalently grafted onto the lignin. Composite cast films based on poly(l-lactide) matrix containing ungrafted lignin (lignin/PLLA), chemically-grafted lignin copolymer (PLA-g-lignin/PLLA) and plasma-treated lignin (plasma-treated lignin/PLLA) were investigated. Differential scanning calorimetry and dynamical mechanical analyses revealed that plasma-treated lignin preserved the crystalline structure of PLLA matrix and had a significant reinforcing effect compared with lignin and PLA-g-lignin. Results were compared with literature data. [Display omitted] •Pyrolitic lignin particle grafted with polylactide chains.•Plasma treated lignin does not disturb the crystallinity of polylactide matrix.•Storage modulus of lignin/polylactide nanocomposite significantly enhanced.•Reinforcing effect compared with reports.
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2017.04.036