Renewable, Degradable, and Chemically Recyclable Cross-Linked Elastomers

被引:81
作者
Brutman, Jacob P. [1 ]
De Hoe, Guilhem X. [1 ]
Schneiderman, Deborah K. [1 ]
Le, Truyen N. [1 ]
Hillmyer, Marc A. [1 ]
机构
[1] Univ Minnesota, Dept Chem, 207 Pleasant St SE, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
EPOXIDIZED SOYBEAN OIL; EPSILON-DECALACTONE; MECHANICAL-PROPERTIES; BLOCK POLYMERS; L-LACTIDE; LINKING; POLYLACTIDE; NETWORKS; CAPROLACTONE; POLY(L-LACTIDE);
D O I
10.1021/acs.iecr.6b02931
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Most commercial elastomers, typified by vulcanized natural rubber, are cross-linked polymers and as such cannot easily be reprocessed or recycled. While some are derived from renewable resources, the majority are produced from petroleum feedstocks and do not easily degrade. In this study, renewable elastomers based on beta-methyl-delta-valerolactone were produced using two different methodologies: (1) tandem copolymerization/cross-linking with a bis(six-membered cyclic carbonate); (2) cross-linking of a linear poly(beta-methyl-delta-valerolactone) homopolymer with a free-radical generator. The mechanical properties of these materials were investigated; tensile strengths of up to 12 MPa and elongations of up to 2000% were observed. Inclusion of a filler (fumed silica) was used to enhance the performance of the elastomers without significant loss of elasticity, with some composites exhibiting tensile strengths nearly double that of the neat elastomer. Aqueous degradation studies indicated that the materials were capable of degradation in acidic and basic conditions at 60 degrees C. Moreover, these cross-linked elastomers can also be chemically recycled, yielding monomer in high purity and yield (>91% and 93%, respectively).
引用
收藏
页码:11097 / 11106
页数:10
相关论文
共 56 条
[1]  
Albertsson AC, 2002, ADV POLYM SCI, V157, P1
[2]   Self-healable polymer networks based on the cross-linking of epoxidised soybean oil by an aqueous citric acid solution [J].
Altuna, Facundo I. ;
Pettarin, Valeria ;
Williams, Roberto J. J. .
GREEN CHEMISTRY, 2013, 15 (12) :3360-3366
[3]  
[Anonymous], 2016, The new plastics economy - rethinking the future of plastics
[4]   Polylactide Vitrimers [J].
Brutman, Jacob P. ;
Delgado, Paula A. ;
Hillmyer, Marc A. .
ACS MACRO LETTERS, 2014, 3 (07) :607-610
[5]   Development of thermal and photochemical strategies for thiol-ene click polymer functionalization [J].
Campos, Luis M. ;
Killops, Kato L. ;
Sakai, Ryosuke ;
Paulusse, Jos M. J. ;
Damiron, Denis ;
Drockenmuller, Eric ;
Messmore, Benjamin W. ;
Hawker, Craig J. .
MACROMOLECULES, 2008, 41 (19) :7063-7070
[6]  
Chen DZ, 2014, RSC POLYM CHEM SER, V8, P112
[7]   Photoinduced Thiol-Ene Crosslinking of Globalide/ε-Caprolactone Copolymers: Curing Performance and Resulting Thermoset Properties [J].
Claudino, Mauro ;
van der Meulen, Inge ;
Trey, Stacy ;
Jonsson, Mats ;
Heise, Andreas ;
Johansson, Mats .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2012, 50 (01) :16-24
[8]   Catalytic insights into acid/base conjugates: highly selective bifunctional catalysts for the ring-opening polymerization of lactide [J].
Coady, Daniel J. ;
Fukushima, Kazuki ;
Horn, Hans W. ;
Rice, Julia E. ;
Hedrick, James L. .
CHEMICAL COMMUNICATIONS, 2011, 47 (11) :3105-3107
[9]   Vitrimers: permanent organic networks with glass-like fluidity [J].
Denissen, Wim ;
Winne, Johan M. ;
Du Prez, Filip E. .
CHEMICAL SCIENCE, 2016, 7 (01) :30-38
[10]   Mechanically Activated, Catalyst-Free Polyhydroxyurethane Vitrimers [J].
Fortman, David J. ;
Brutman, Jacob P. ;
Cramer, Christopher J. ;
Hillmyer, Marc A. ;
Dichtel, William R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (44) :14019-14022