journal article Open Access Jan 01, 2023

Lignin-derivable alternatives to petroleum-derived non-isocyanate polyurethane thermosets with enhanced toughness

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Abstract
Lignin-derivable non-isocyanate polyurethane thermosets are highlighted as potential alternatives to petroleum-derived analogues with significant enhancement in toughness without compromising other application-specific thermomechanical properties.
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References
54
[1]
Carre ChemSusChem (2019) 10.1002/cssc.201900737
[2]
Gomez-Lopez Chem. Commun. (2021) 10.1039/d1cc05009e
[3]
Kathalewar RSC Adv. (2013) 10.1039/c2ra21938g
[4]
Liang Environ. Sci. Technol. (2021) 10.1021/acs.est.1c03654
[5]
M.Szycher , Szycher's handbook of polyurethanes , CRC Press , Boca Raton, FL , 2nd edn, 2013
[6]
Cornille Eur. Polym. J. (2017) 10.1016/j.eurpolymj.2016.11.027
[7]
Market volume of polyurethane worldwide from 2015 to 2025, with a forecast for 2022 to 2029 (in million metric tons), https://www.chemintel360.com/reportdetails/Global-Polyurethane-Market/25 , accessed September 3, 2022
[8]
Bio-based Building Blocks and Polymers – Global Capacities, Production and Trends 2020 – 2025, https://renewable-carbon.eu/publications/product/bio-based-building-blocks-and-polymers-global-capacities-production-and-trends-2020-2025-graphics-figure-6/ , accessed September 3, 2022
[9]
Besse React. Funct. Polym. (2013) 10.1016/j.reactfunctpolym.2013.01.002
[10]
Meng Ind. Crops Prod. (2022) 10.1016/j.indcrop.2022.114579
[11]
Al Meselmani Nat. Rev. Earth Environ. (2020) 10.1038/s43017-020-0081-7
[12]
Chen ACS Appl. Mater. Interfaces (2019) 10.1021/acsami.8b19100
[13]
Fortman J. Am. Chem. Soc. (2015) 10.1021/jacs.5b08084
[14]
Chen Polym. Chem. (2017) 10.1039/c7py01160a
[15]
Chen Green Chem. (2015) 10.1039/c5gc01340b
[16]
Janvier ACS Sustainable Chem. Eng. (2017) 10.1021/acssuschemeng.7b01271
[17]
Mahajan ACS Sustainable Chem. Eng. (2020) 10.1021/acssuschemeng.0c04817
[18]
Mhd Haniffa Chem. – Asian J. (2021) 10.1002/asia.202100226
[19]
Ghasemlou Eur. Polym. J. (2019) 10.1016/j.eurpolymj.2019.06.032
[20]
Salanti RSC Adv. (2017) 10.1039/c7ra03416d
[21]
Hu ACS Sustainable Chem. Eng. (2019) 10.1021/acssuschemeng.9b01239
[22]
Dong Polym. Chem. (2020) 10.1039/d0py01249a
[23]
Bähr Green Chem. (2012) 10.1039/c2gc16230j
[24]
Fleischer Green Chem. (2013) 10.1039/c3gc00078h
[25]
Tamami J. Appl. Polym. Sci. (2004) 10.1002/app.20049
[26]
Webster Prog. Org. Coat. (2003) 10.1016/s0300-9440(03)00074-2
[27]
Koelewijn Green Chem. (2017) 10.1039/c7gc00776k
[28]
Yang ACS Sustainable Chem. Eng. (2016) 10.1021/acssuschemeng.6b01343
[29]
Defining the Macromolecules of Tomorrow through Synergistic Sustainable Polymer Research

Farihah M. Haque, Jacob S. A. Ishibashi, Claire A. L. Lidston et al.

Chemical Reviews 2022 10.1021/acs.chemrev.1c00173
[30]
Potential Lignin-Derived Alternatives to Bisphenol A in Diamine-Hardened Epoxy Resins

Kaleigh H. Nicastro, Christopher J. Kloxin, Thomas H. Epps, III

ACS Sustainable Chemistry & Engineering 2018 10.1021/acssuschemeng.8b03340
[31]
Zhao ACS Sustainable Chem. Eng. (2016) 10.1021/acssuschemeng.6b01446
[32]
Lignin Valorization: Improving Lignin Processing in the Biorefinery

Arthur J. Ragauskas, Gregg T. Beckham, Mary J. Biddy et al.

Science 2014 10.1126/science.1246843
[33]
Jawerth RSC Adv. (2016) 10.1039/c6ra21447a
[34]
Gioia J. Am. Chem. Soc. (2018) 10.1021/jacs.7b13620
[35]
Bass Polym. Chem. (2021) 10.1039/d1py00694k
[36]
Gillet Green Chem. (2017) 10.1039/c7gc01479a
[37]
Chemicals from lignin: an interplay of lignocellulose fractionation, depolymerisation, and upgrading

W. Schutyser, T. Renders, S. Van den Bosch et al.

Chemical Society Reviews 2018 10.1039/c7cs00566k
[38]
Rafiee J. Am. Chem. Soc. (2019) 10.1021/jacs.9b07243
[39]
Bright Side of Lignin Depolymerization: Toward New Platform Chemicals

Zhuohua Sun, Bálint Fridrich, Alessandra de Santi et al.

Chemical Reviews 2018 10.1021/acs.chemrev.7b00588
[40]
100th Anniversary of Macromolecular Science Viewpoint: Polymers from Lignocellulosic Biomass. Current Challenges and Future Opportunities

Robert M. O’Dea, Jordan A. Willie, Thomas H. Epps

ACS Macro Letters 2020 10.1021/acsmacrolett.0c00024
[41]
Peng Food Chem. (2021) 10.1016/j.foodchem.2020.127656
[42]
Estrogenic activity of lignin-derivable alternatives to bisphenol A assessed via molecular docking simulations

Alice Amitrano, Jignesh S. Mahajan, LaShanda T. J. Korley et al.

RSC Advances 2021 10.1039/d1ra02170b
[43]
Hernandez ACS Sustainable Chem. Eng. (2016) 10.1021/acssuschemeng.6b00835
[44]
Llevot Macromol. Rapid Commun. (2016) 10.1002/marc.201500474
[45]
Zhao ACS Sustainable Chem. Eng. (2018) 10.1021/acssuschemeng.8b00443
[46]
Yamamoto RSC Adv. (2020) 10.1039/d0ra05671e
[47]
Harvey Macromolecules (2015) 10.1021/acs.macromol.5b00496
[48]
Farhadian Polym. Degrad. Stab. (2018) 10.1016/j.polymdegradstab.2018.07.010
[49]
Delebecq Chem. Rev. (2013) 10.1021/cr300195n
[50]
A. J.Kinloch and R. J.Young , in Fracture Behaviour of Polymers , ed. A. J. Kinloch and R. J. Young , Springer Netherlands , Dordrecht , 1995 10.1007/978-94-017-1594-2

Showing 50 of 54 references

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