Issue 34, 2024, Issue in Progress

Development of an assay for colorimetric and fluorometric detection of H2S

Abstract

Hydrogen sulfide is a highly toxic gas that can produce extremely rapid CNS and respiratory depression and sometimes becomes fatal at high concentrations. There is no proven antidote for hydrogen sulfide poisoning. Hence, it is important to reduce the production of H2S in several industries, such as oil and gas refining and mining industries. As a consequence, researchers are always inquisitive about inventing different sensing devices or useful tools to detect H2S selectively in a cost-effective manner. Colorimetric and fluorometric detection methods are the most attractive owing to their simplicity, profitability, ease of understanding, and “on-spot” detection convenience. In this research, we developed some colorimetric and fluorometric chemosensors and established an assay for the easy detection of H2S following a specific mechanism. The sensing mechanisms were well established through exhaustive spectroscopic studies and theoretical calculations. We first synthesized a series of chemosensors using 2-hydroxy naphthaldehyde as a primary fluorophore. The chemosensors were developed by incorporating various electron-releasing and donating groups while keeping the binding site unchanged. Subsequently, we compared their efficiency and binding ability towards H2S with a possible mechanism. The chemosensor was employed through a paper strip for demonstration as an “in-field” device by changing the naked-eye and fluorescence color both in liquid and gas phases.

Graphical abstract: Development of an assay for colorimetric and fluorometric detection of H2S

Supplementary files

Article information

Article type
Paper
Submitted
13 Jun 2024
Accepted
27 Jul 2024
First published
12 Aug 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 25071-25076

Development of an assay for colorimetric and fluorometric detection of H2S

P. Ghosh, D. De and P. Sahoo, RSC Adv., 2024, 14, 25071 DOI: 10.1039/D4RA04339A

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