Synthesis of High-Performance Lignin-Based Inverse Thermoplastic Vulcanizates with Tailored Morphology and Properties AITranslate
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We report synthesis of a high-strength renewable phenolic composition with linear large deformation strain without a thermoplastic-like yielding while retaining thermal processability. Small molecule carboxylic acid derivatives with varying molecular architectures act as esterifying crosslinkers in an equal mass mixture of lignin and acrylonitrile–butadiene copolymers in a highly scalable, solvent-free process. These “inverse thermoplastic vulcanizates” (iTPVs)─unique in their approach of crosslinking the rigid lignin phase rather than the soft phase─exhibit ordered self-assembly, tunable nanoscale morphology, and processability. The first of its kind iTPV compositions exhibit engineering stress–strain curves with two- to sixfold linear extensibility, a twofold rise in strength, and an order of magnitude enhanced modulus compared to a simple lignin-rubber blend. Viscoelastic properties correlate well with crosslinker architecture and the resulting morphology, allowing competing properties of toughness and stiffness to be tuned. This research finds a path for identifying the potential of lignin as a sustainable feedstock.
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DOI:https://doi.org/10.1021/acsapm.0c01387
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We report synthesis of a high-strength renewable phenolic composition with linear large deformation strain without a thermoplastic-like yielding while retaining thermal processability. Small molecule carboxylic acid derivatives with varying molecular architectures act as esterifying crosslinkers in an equal mass mixture of lignin and acrylonitrile–butadiene copolymers in a highly scalable, solvent-free process. These “inverse thermoplastic vulcanizates” (iTPVs)─unique in their approach of crosslinking the rigid lignin phase rather than the soft phase─exhibit ordered self-assembly, tunable nanoscale morphology, and processability. The first of its kind iTPV compositions exhibit engineering stress–strain curves with two- to sixfold linear extensibility, a twofold rise in strength, and an order of magnitude enhanced modulus compared to a simple lignin-rubber blend. Viscoelastic properties correlate well with crosslinker architecture and the resulting morphology, allowing competing properties of toughness and stiffness to be tuned. This research finds a path for identifying the potential of lignin as a sustainable feedstock.
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| GB/T 7714-2015 | [1] Nihal Kanbargi, Monojoy Goswami, Liam Collins, et al. ACS Applied Polymer Materials, 2021(3). DOI:10.1021/acsapm.0c01387. |
| MLA | [1] Nihal Kanbargi, et al., ACS Applied Polymer Materials, no. 3, 2021, https://doi.org/10.1021/acsapm.0c01387. |
| APA | [1] Nihal Kanbargi, Monojoy Goswami, Liam Collins, Logan T Kearney, Christopher C Bowland, Keonhee Kim, Kalavathy Rajan, Nicole Labbe, & Amit K Naskar. (2021). ACS Applied Polymer Materials(3). https://doi.org/10.1021/acsapm.0c01387 |
| IEEE | [1] Nihal Kanbargi, Monojoy Goswami, Liam Collins, Logan T Kearney, Christopher C Bowland, Keonhee Kim, Kalavathy Rajan, Nicole Labbe, and Amit K Naskar, ACS Applied Polymer Materials, no. 3, 2021, doi: 10.1021/acsapm.0c01387. keywords: {sustainable thermoplastics;inverse thermoplastic vulcanizate;multiphase polymers;renewable feedstock;lignin valorization} |
