Capturing carbon dioxide as a polymer from natural gas

Chih-Chau Hwang; Josiah J Tour; Carter Kittrell; Laura Espinal; Lawrence B Alemany; James M Tour

doi:10.1038/ncomms4961

Capturing carbon dioxide as a polymer from natural gas

Nat Commun. 2014 Jun 3:5:3961. doi: 10.1038/ncomms4961.

Authors

Chih-Chau Hwang¹, Josiah J Tour¹, Carter Kittrell², Laura Espinal³, Lawrence B Alemany⁴, James M Tour⁵

Affiliations

¹ Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, USA.
² The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, 6100 Main Street, Houston, Texas 77005, USA.
³ Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA.
⁴ 1] Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, USA [2] The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, 6100 Main Street, Houston, Texas 77005, USA [3] Shared Equipment Authority, Rice University, 6100 Main Street, Houston, Texas 77005, USA.
⁵ 1] Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, USA [2] The Richard E. Smalley Institute for Nanoscale Science and Technology, Rice University, 6100 Main Street, Houston, Texas 77005, USA [3] The Department of Materials Science and NanoEngineering, Rice University, 6100 Main Street, Houston, Texas 77005, USA.

Abstract

Natural gas is considered the cleanest and recently the most abundant fossil fuel source, yet when it is extracted from wells, it often contains 10-20 mol% carbon dioxide (20-40 wt%), which is generally vented to the atmosphere. Efforts are underway to contain this carbon dioxide at the well-head using inexpensive and non-corrosive methods. Here we report nucleophilic porous carbons are synthesized from simple and inexpensive carbon-sulphur and carbon-nitrogen precursors. Infrared, Raman and (13)C nuclear magnetic resonance signatures substantiate carbon dioxide fixation by polymerization in the carbon channels to form poly(CO2) under much lower pressures than previously required. This growing chemisorbed sulphur- or nitrogen-atom-initiated poly(CO2) chain further displaces physisorbed hydrocarbon, providing a continuous carbon dioxide selectivity. Once returned to ambient conditions, the poly(CO2) spontaneously depolymerizes, leading to a sorbent that can be easily regenerated without the thermal energy input that is required for traditional sorbents.

Publication types

Research Support, Non-U.S. Gov't
Retracted Publication