Thursday, 5 October 2006
South Ballroom (Binghamton Regency Hotel and Conference Center)
129

Synthesis of Nanostructured Activated Carbons from Lignin and Their Application in Hydrogen Storage

Suoding Li, Xinwei Wang, Youxin Yuan, and Israel Cabasso. State University of New York-ESF, Syracuse, NY

Onboard hydrogen storage is one of the major hurdles in developing hydrogen fuel cell-powered vehicles. Cryogenic physisorption on nanostructured carbons exhibits the potential to meet the DOE 2010 hydrogen storage capacity target (~ 7 wt%). This research is focused on tailoring the pore structure of lignin-derived activated carbons for hydrogen storage.

A series of nanostructured activated carbons have been synthesized from lignin, a pulp industry waste, by carbonization and activation. Thermogravimetric analysis and pyrolysis-MS studies revealed that CO, CO2 and H2O are the primary thermodegradation products during the carbonization process, leading to a high yield of lignin carbon (> 50 wt%). Nanoporous structure is formed and tuned by activating lignin carbon matrix with activating agents CO2, K2CO3 and KOH at a temperature range of 600 to 850 °C. Nitrogen sorption results revealed that activated lignin carbons are highly porous, with the majority of pores having a pore diameter less than 2 nm. Hydrogen uptake at 1 bar and 77 K indicates that high surface area and small pore size facilitate hydrogen uptake. A hydrogen storage capacity of ~ 2.4 wt% (77 K, 1 bar) has been recorded for an activated lignin carbon with a surface area of ~ 2000 m2/g and an average pore diameter of dDR ~ 1.4 nm.

 


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