Bio-based non-isocyanate poly(hydroxy urethane)s (PHU) derived from vanillin and CO2

被引:10
作者
Fanjul-Mosteirin, Noe [1 ,2 ,3 ]
Fonseca, Lucas Polo [3 ]
Dove, Andrew P. P. [2 ]
Sardon, Haritz [3 ]
机构
[1] Univ Warwick, Dept Chem, Gibbet Hill Rd, Coventry CV4 7AL, England
[2] Univ Birmingham, Sch Chem, Birmingham B15 2TT, England
[3] Univ Basque Country UPV EHU, Joxe Mari Korta Ctr, POLYMAT, Avda Tolosa 72, Donostia San Sebastian 20018, Spain
来源
MATERIALS ADVANCES | 2023年 / 4卷 / 11期
关键词
CYCLIC CARBONATES; FREE ROUTES; POLYURETHANES; EPOXIDES; AMINES; CHEMISTRY; DIOXIDE; LIGNIN;
D O I
10.1039/d3ma00111c
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
As an alternative to the use of hazardous phosgene-based isocyanates for polyurethane preparation, non-isocyanate poly(hydroxy urethanes) (PHU) based on 5-membered cyclic carbonates have been developed. However, to date, most aromatic PHUs are oil-based or based on toxic precursors such as bisphenol-A. In this work, bio-based non-isocyanate poly(hydroxy urethanes) (PHUs) prepared from vanillin are reported for the first time. First, three different vanillin-derived bis-cyclic carbonates were synthesized. Subsequently, each monomer was reacted with two different bis-amines to yield six different PHUs, which were characterized in depth by H-1 and C-13 NMR spectroscopy, FTIR, SEC and DSC. PHUs based on vanillic acid were found to exhibit thermal properties superior to bisphenol A-based PHUs, with a T-g of around 66 degrees C. It is envisioned that vanillin-based PHUs could potentially be a safer alternative to harmful bisphenol A-based PHUs and provide a useful strategy for CO2 revalorization, especially considering that vanillin is an abundant byproduct of Kraft lignin production.
引用
收藏
页码:2437 / 2448
页数:12
相关论文
共 65 条
[1]   PU foam derived from renewable sources: Perspective on properties enhancement: An overview [J].
Agrawal, Anuja ;
Kaur, Raminder ;
Walia, R. S. .
EUROPEAN POLYMER JOURNAL, 2017, 95 :255-274
[2]   Polyurethane types, synthesis and applications - a review [J].
Akindoyo, John O. ;
Beg, M. D. H. ;
Ghazali, Suriati ;
Islam, M. R. ;
Jeyaratnam, Nitthiyah ;
Yuvaraj, A. R. .
RSC ADVANCES, 2016, 6 (115) :114453-114482
[3]   Organocatalyzed coupling of carbon dioxide with epoxides for the synthesis of cyclic carbonates: catalyst design and mechanistic studies [J].
Alves, M. ;
Grignard, B. ;
Mereau, R. ;
Jerome, C. ;
Tassaing, T. ;
Detrembleur, C. .
CATALYSIS SCIENCE & TECHNOLOGY, 2017, 7 (13) :2651-2684
[4]   Optimizing conductivity and cationic transport in crosslinked solid polymer electrolytes [J].
Baroncini, Elyse A. ;
Rousseau, Dominique M. ;
Strekis, Christopher A. ;
Stanzione, Joseph F., III .
SOLID STATE IONICS, 2020, 345 (345)
[5]   *DAS DI-ISOCYANAT-POLYADDITIONSVERFAHREN (POLYURETHANE) [J].
BAYER, O .
ANGEWANDTE CHEMIE, 1947, 59 (09) :257-272
[6]   Barriers to Rotation in ortho-Substituted Tertiary Aromatic Amides: Effect of Chloro-Substitution on Resonance and Distortion [J].
Bisz, Elwira ;
Piontek, Aleksandara ;
Dziuk, Blazej ;
Szostak, Roman ;
Szostak, Michal .
JOURNAL OF ORGANIC CHEMISTRY, 2018, 83 (06) :3159-3163
[7]   Water-based non-isocyanate polyurethane-ureas (NIPUUs) [J].
Bizet, Boris ;
Grau, Etienne ;
Cramail, Henri ;
Asua, Jose M. .
POLYMER CHEMISTRY, 2020, 11 (23) :3786-3799
[8]   Isocyanate- and Phosgene-Free Routes to Polyfunctional Cyclic Carbonates and Green Polyurethanes by Fixation of Carbon Dioxide [J].
Blattmann, Hannes ;
Fleischer, Maria ;
Baehr, Moritz ;
Muelhaupt, Rolf .
MACROMOLECULAR RAPID COMMUNICATIONS, 2014, 35 (14) :1238-1254
[9]   ORGANOMETALLIC REACTIONS .I. ADDITION OF TIN ALKOXIDES TO ISOCYANATES [J].
BLOODWORTH, AJ ;
DAVIES, AG .
JOURNAL OF THE CHEMICAL SOCIETY, 1965, (OCT) :5238-+
[10]   Non-Isocyanate Polyurethane Soft Nanoparticles Obtained by Surfactant-Assisted Interfacial Polymerization [J].
Bossion, Amaury ;
Jones, Gavin O. ;
Taton, Daniel ;
Mecerreyes, David ;
Hedrick, James L. ;
Ong, Zhan Yuin ;
Yang, Yi Yan ;
Sardon, Haritz .
LANGMUIR, 2017, 33 (08) :1959-1968