Related Experiment Video
Updated: Nov 1, 2025

Author Spotlight: Standardizing the Development of Amine-Based Silica Composites as CO2 Adsorbents for Direct Air Capture
Published on: September 29, 2023
New chemistry for enhanced carbon capture: beyond ammonium carbamates
Alexander C Forse1, Phillip J Milner2
1Department of Chemistry, University of Cambridge Cambridge CB2 1EW UK acf50@cam.ac.uk.
Abstract:
Carbon capture and sequestration is necessary to tackle one of the biggest problems facing society: global climate change resulting from anthropogenic carbon dioxide (CO2) emissions. Despite this pressing need, we still rely on century-old technology-aqueous amine scrubbers-to selectively remove CO2 from emission streams. Amine scrubbers are effective due to their exquisite chemoselectivity towards CO2 to form ammonium carbamates and (bi)carbonates, but suffer from several unavoidable limitations. In this perspective, we highlight the need for CO2 capture via new chemistry that goes beyond the traditional formation of ammonium carbamates. In particular, we demonstrate how ionic liquid and metal-organic framework sorbents can give rise to capture products that are not favourable for aqueous amines, including carbamic acids, carbamate-carbamic acid adducts, metal bicarbonates, alkyl carbonates, and carbonic acids. These new CO2 binding modes may offer advantages including higher sorption capacities and lower regeneration energies, though additional research is needed to fully explore their utility for practical applications. Overall, we outline the unique challenges and opportunities involved in engineering new CO2 capture chemistry into next-generation technologies.
More Related Videos
Related Concept Videos
Metabolism of Chemolithotrophs
Carbocations
¹³C NMR: ¹H–¹³C Decoupling
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
2° Amines to N-Nitrosamines: Reaction with NaNO2

