Journal
POLYMER CHEMISTRY
Volume 7, Issue 33, Pages 5233-5240Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6py00700g
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Funding
- Wayland E. Noland Fellowship of the chemistry department at the University of Minnesota
- National Science Foundation under the Center for Sustainable Polymers [CHE-1413862]
- NSF through the UMN MRSEC program under Award [DMR-1420013]
- E. I. DuPont de Nemours Co.
- Dow Chemical Company
- Northwestern University
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1413862] Funding Source: National Science Foundation
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Herein, we present the direct modification of glucose, an abundant and inexpensive sugar molecule, to produce new sustainable and functional polymers. Glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) has been synthesized and shown to provide a useful glassy component for developing an innovative family of elastomeric and adhesive materials. A series of diblock and triblock copolymers of GATA and n-butyl acrylate (n-BA) were created via Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization. Initially, poly(GATA)-b-poly(n-BA) copolymers were prepared using 4-cyano-4-[(ethylsulfanylthiocarbonyl) sulfanyl] pentanoic acid (CEP) as a chain transfer agent (CTA). These diblock copolymers demonstrated decomposition temperatures of 275 degrees C or greater and two glass transition temperatures (T-g) around -45 degrees C and 100 degrees C corresponding to the PnBA and PGATA domains, respectively, as measured by differential scanning calorimetry (DSC). Triblock copolymers of GATA and n-BA, with moderate dispersities (D = 1.15-1.29), were successfully synthesized when S, S-dibenzyl trithiocarbonate (DTC) was employed as the CTA. Poly(GATA)-b-poly(nBA)-b-poly(GATA) copolymers with 14-58 wt% GATA were prepared and demonstrated excellent thermomechanical properties (T-d >= 279 degrees C). Two well-separated glass transitions near the values for homopolymers of n-BA and GATA (similar to-45 degrees C and similar to 100 degrees C, respectively) were measured by DSC. The triblock with 14% GATA exhibited peel adhesion of 2.31 N cm(-1) (when mixed with 30 wt% tackifier) that is superior to many commercial pressure sensitive adhesives (PSAs). Use of 3,5-bis(2-dodecylthiocarbonothioylthio-1oxopropoxy) benzoic acid (BTCBA) as the CTA provided a more efficient route to copolymerize GATA and n-BA. Using BTCBA, poly(GATA)-b-poly(nBA)-b-poly (GATA) triblock copolymers containing 12-25 wt% GATA, with very narrow molar mass distributions (D = 1.08), were prepared. The latter series of triblock copolymers showed excellent thermal stability with Td = 275 degrees C. Only the Tg for the PnBA block was observed by DSC (similar to-45 degrees C), however, phase-separation was confirmed by small-angle X-ray scattering (SAXS) for all of these triblock copolymers. The mechanical behavior of the polymers was investigated by tensile experiments and the triblock with 25% GATA content demonstrated moderate elastomeric properties, 573 kPa stress at break and 171% elongation. This study introduces a new family of glucose-based ABA-type copolymers and demonstrates functionality of a glucose-based feedstock for developing green polymeric materials.
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