Related Experiment Video
Updated: Feb 8, 2026

Aqueous Droplets Used as Enzymatic Microreactors and Their Electromagnetic Actuation
Published on: August 28, 2017
Analysis of Carbonyl Compounds in Ambient Air by a Microreactor Approach
Mingxiao Li1, Qi Li1, Michael H Nantz1
1Department of Chemical Engineering and Department of Chemistry, University of Louisville, 216 Eastern Parkway, Louisville, Kentucky 40208, United States.
Abstract:
Aldehydes including formaldehyde, acetaldehyde, and acrolein are toxic organic components of air pollution that cause lung cancer and cardiovascular disease with chronic exposure. The commonly used method for determining the levels of carbonyl compounds based on the derivatizing agent 2,4-dinitrophenylhydrazine is of limited use for ketones and unsaturated aldehydes because of issues such as low capture efficiencies, unstable derivatives, and long sample collection times. This work details the analysis of carbonyls in ambient air by a microreactor approach. The microreactor is fabricated on a silicon wafer and has thousands of micropillars in a microfluidic channel for uniformly distributing the air flow through the channel. The surfaces of the micropillars are coated with a quaternary ammonium aminooxy reagent, 2-(aminooxy)ethyl-N,N,N-trimethylammonium iodide (ATM), for chemoselective capture of carbonyl compounds by means of oximation reactions. ATM-carbonyl adducts are eluted from the microreactor and directly analyzed by Fourier transform ion cyclotron resonance mass spectrometry and ultrahigh-performance liquid chromatography-mass spectrometry. More than 20 carbonyls were detected in ambient air samples. Acetone, 2-butanone, acetaldehyde, and formaldehyde were the most abundant carbonyls in ambient air of the studied urban areas.
Related Concept Videos
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Alcohols from Carbonyl Compounds: Grignard Reaction
Magnesium from the reagent coordinates with carbonyl oxygen, further reducing the carbonyl carbon's electron density. Thus, the...
Conjugate Addition to α,β-Unsaturated Carbonyl Compounds
Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
Nucleophilic Addition to the Carbonyl Group: General Mechanism
A stronger nucleophile can directly attack the electrophilic center, the carbonyl carbon. The HOMO orbital of the nucleophile interacts with the LUMO (π* antibonding) orbital present on the carbonyl carbon. This interaction breaks the π bond and shifts the π...
Molecules and Compounds

