Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

Reversible CO2 adsorption by an activated nitrogen doped graphene/polyaniline material.

Nanotechnology 2013 June 15
For effective adsorption of carbon dioxide (CO2), we investigate a porous N functionalized graphene adsorbent produced by the chemical activation of a reduced graphene oxide/polyaniline composite. The N-doped graphene composite is microporous with a maximum BET surface area of 1336 m(2) g(-1). It shows a highly reversible maximum CO2 storage capacity of 2.7 mmol g(-1) at 298 K and 1 atm (5.8 mmol g(-1) at 273 K and 1 atm). The N-doped graphene shows good stability during recycling with only an initial decrease of 10% (3-2.7 mmol g(-1)) in adsorption capacity before attaining a cycling equilibrium. The adsorbance capacity is correlated with N content × pore volume or N content × surface area. Given that there is no proper correlation parameter, these factors can be used to increase the CO2 adsorption capacity of N-doped graphene materials for practical utility. The as synthesized material also displays selectivity towards CO2 adsorption compared to H2, N2, Ar or CH4. The as formed material shows that graphene can be uniformly N-doped using the presented synthetic method.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app