Functional Polymers From Renewable Resources S. Shang, A. Ro, S. J. Huang and R. A. Weiss Polymer Program University of Connecticut Storrs, CT New England.

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Functional Polymers From Renewable Resources S. Shang, A. Ro, S. J. Huang and R. A. Weiss Polymer Program University of Connecticut Storrs, CT New England Green Chemistry Consortium Annual Meeting University of Maine Orno, ME May 31, 2006

Monomers From Renewable Resources Polymers based on renewable resources crops, grasses, agricultural byproducts Raw materials are sustainable; Polymers can be designed to be biodegradable Lactic AcidItaconic Anhydride Stearyl Methacrylate Fermentation of agricultural by-products (carbohydrates), e.g., corn starch Pyrolysis of citric acid, or Fermentation of carbohydrates to form itaconic acid, followed by dehydration Derived from fatty acid from animal or vegetable fats or oils

Poly(lactic acid), PLA Drumwright, R. E.; Gruber, P. R.; Henton, D. E. Adv. Mater Applications: Fibers, films, moldable thermoplastics (T m ~ 175  C), sutures Deficiencies: Low T g (~ 60  C), Narrow melt processing window, Brittle plastic, hydrophobic; incompatible with other polymers (blends)

Ionomers Predominantly hydrophobic polymers that contain modest amounts of bonded acid or salt groups (~ 15 mol%) Interchain association of salt groups significantly alters thermal properties, mechanical properties and rheology. PS 1.82 NaSPS 3.44 NaSPS 5.81 NaSPS Applications: coatings, fibers, thermoplastics, adhesion promoters, compatibilizers, viscosifiers, permselective membranes, hydrogels…

Research Goals Synthesize and Characterize Ionomers Derived from Lactic Acid, Itaconic Anhydride and Stearyl Methacrylate Random Ionomer - + Telechelic Ionomer - + ITA SM ITA PLA

Radical copolymerizaton of ITA and SM IR evidence for copolymerizaiton: 1862, 1782 cm -1 : ITA (anhydride) 5 member ring shift of C=O in SM from 1720 to 1731 cm -1 indicating reaction of C=C disappearance of peak at 1601 cm -1 : reaction of C=C 1601 Mixture Copolymer

r ITA = r 1 = 0.53 r SM = r 2 = 0.12 Random Copolymers Copolymerization of ITA and SM M n (25k – 60kDa) decreased with increasing f ITA J. Wallach, PhD Dissertation, Univ. Conn., 2000

Thermal behavior of ITA-co-SM copolymers Increasing SM composition f ITA M n (kDa)T m (  C)  H (J/g SM) Crystallinity is due to the SM side chain packing Melting temperature increased with increasing ITA content! Effect of ITA on crystallinity was complicated. No glass transition was observed (T g(ITA) ~ 130  C). DSC: 1 st scan after ppt from soln.

Crystalline structure of ITA-co-SM Composition (mol% ITA)d (nm) Length of alkyl side chain = 2.5 nm SAXS WAXD nm characteristic of n-alkyl hexagonal packing,

27  3.9 nm Zn-Stearate Bilayer Crystal Side-Chain, Stearyl Methacrylate Crystals L L Intercalated Crystal Bilayer Crystal L

(M n =33 kDa; 40 mol% ITA) IR evidence of neutralization Peak ~ cm -1 due to COO - ITA-co-SM Ionomers

Ionomer Structure and Properties Ionic aggregation was observed Long spacing of SM crystals increased upon neutralization Neutralization increased the elasticity of the polymer. TMA (F = 60 mN) SAXS

Chemical Recycling of PLA by Transesterification Transesterification  Uncatalyzed - slow process, reaction temperature  C.  Catalyzed - lower time and temperature (J. Wallach, PhD Dissertation, Univ. Conn., 2000). –SnOct 2. FDA approved. Mechanism

Synthesis of ω-carboxylate functionalized PLA A. Synthesis of methacrylate-terminated PLA B. Functionalization with itaconic anhydride

Broad OH stretch Carboxylic C=O stretch C-O-H in-plane bend and C-O stretch C=C stretch C=O stretch

A symmetric carboxylate anion stretch

1 H-NMR Spectrum of Functionalized PLA Oligomer End group Analysis - M n = 1930, with 25 LLA units c d h d c h

For higher molecular weight (M ~ 15,000 – 900,000), T g was relatively insensitive to functionalization Glass Transition Temperatures of PLA-ITA Telechelic Ionomers Cations = Li +, Na +, K +, Ca 2+, Zn 2+, Y 3+ YZn Ca LiNa K

Acknowledgments Funding by: New England Green Chemistry Consortium NSF/EPA

Petroleum-Based Polymers Hydrophobic and resistant to biodegradation Escalating prices of petroleum (only ~ 2% of petroleum is used for polymers) *Municipal Solid Waste Generation, Recycling, and Disposal in the United States: Facts and Figures for 2003, U.S. Environmental Protection Agency, Tullo, Chem. Eng. News. 2005, 83, 19. *

Environmental Concerns Plastic are the largest volume component in U.S. landfills (~ 25%) Existing petroleum resources are limited. Plastics production has nearly doubled every 10 years for four decades. Environmental Issue Sustainability Issue

Biodegradable Polymers Aliphatic Polyesters from Hydroxyacids Poly(3-hydroxybutyric acid) Poly(lactic acid) NatureWorks LLC

Itaconic Anhydride Ramos – PEG functionalization Biocompatible – citric acid distillation, fermentation of carbohydrates (Aspergillus terreus) Ramos, M. Multi-component Hydrophilic-Hydrophobic Systems From Itaconic Anhydride. Ph.D. Thesis, University of Connecticut, Storrs, CT, 2002.