Biomass‐Based H <sub>2</sub> S Scavengers: Michael Acceptors

Michael acceptors derived from biomass resources, such as carbohydrates, have been synthesized and their H 2 S scavenging properties studied. The most promising candidates were compared with the commercial H 2 S scavenger MEA‐triazine by studying the aqueous phase scavenging reactions using in situ Raman spectroscopy and the gas–liquid reactions were evaluated in a flow setup. Based on cost and scavenging efficiency considerations, the industrially most promising candidates were submitted to ecotoxicity studies. We have found three families of Michael acceptors, which are readily available and can be tailor‐made to serve as sulfide scavengers under different conditions.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-01-27
DOI
https://doi.org/10.1002/ejoc.202501122
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Biomass‐Based H 2 S Scavengers: Michael Acceptors

Jesper Bendix, Victor Friis, Asger Munk Koue, Lars Skjolding et al.
European Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
article

Biomass‐Based H 2 S Scavengers: Michael Acceptors

Jesper Bendix, Victor Friis, Asger Munk Koue, Lars Skjolding, Xifu Liang, Karolina Agata Szlek, Christian Marcus Pedersen, Sergey Kucheryavskiy, Marco Maschietti
article en

Abstract

Michael acceptors derived from biomass resources, such as carbohydrates, have been synthesized and their H 2 S scavenging properties studied. The most promising candidates were compared with the commercial H 2 S scavenger MEA‐triazine by studying the aqueous phase scavenging reactions using in situ Raman spectroscopy and the gas–liquid reactions were evaluated in a flow setup. Based on cost and scavenging efficiency considerations, the industrially most promising candidates were submitted to ecotoxicity studies. We have found three families of Michael acceptors, which are readily available and can be tailor‐made to serve as sulfide scavengers under different conditions.

European Journal of Organic ChemistryVol. 29(8)
University of Copenhagen (DK), Novo Nordisk (Denmark) (DK), Aalborg University (DK), Technical University of Denmark (DK)
Openalex Percentile: Top 77%
Sulfur-Based Synthesis Techniques
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