Polymers from Cellulose Waste Products

Overview:
James A. Moore launched innovative research in 1997 representing recycling at a fundamentally efficient level: using waste cellulose such as by-products left over in the paper-making process as a source of intermediates to make polymers, copolymers and blends. Other cellulose-rich sources include wood, sewage sludge, and food processing waste. This research is funded in part by the NYS Energy Research and Development Administration and by Biofine, a bioengineering firm headquartered in Massachusetts.

Moore’s utilization of recycled materials normally routed to the nearest landfill won a Presidential Green Chemistry Challenge Award, presented last year by then-Vice President Al Gore. The annual awards recognize outstanding chemical technologies that incorporate green chemistry principles into chemical design, manufacture, and use.

“Our research is economically driven in that we’re finding use for a waste source, and right now paper plants pay a fee to have it carted away to the dump, so they’re willing to give it away for research,” said Moore. “Our original project was to identify a niche market for the DPA, and we’ve done that and gone beyond. Our research is an open door from here on out.”

Technical Description:
During Moore’s research, materials derived from the monomer such as polycarbonate homo- and co-polymers (with bis-phenol A, BPA) are prepared and their properties studied. The influence of copolymer composition on the thermal properties of these materials has been determined, and the blends of polycarbonates from BPA and from DPA appear to be compatible with each other. Soluble but highly branched polyester can be prepared from bis-acetoxy DPA by a thermally induced polycondensation interchange reaction with the elimination of acetic acid. Extremely high apparent molecular weights are attainable in this way.

The preparation of the t-butyl ester of DPA enables the formation of homo- and co-polycarbonates in which the blocking group can be removed to give free carboxyl groups along the polymer backbone. Such materials exhibit classic polyelectrolyte behavior. The sodium salt of the homo-polycarbonate carboxylate is surprisingly stable to hydrolysis in alkaline solutions. Neutralization of the carboxyl groups with polyvalent counter ions leads to cross-linked gels. The carboxyl groups can also serve as the locus for grafting reactions leading to materials with unusual properties.

Contact Information:

Prof. James A. Moore
Professor, Department of Chemistry
Rensselaer Polytechnic Institute
110 8th Street
Troy, NY 12180-3590
(518) 276-8481
moorej@rpi.edu

 

 

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