Effects of internal hydrophilic groups of a newly developed sustainable anionic surfactant on biodegradability and ecotoxicity.
Biodegradation
Ecotoxicity
Internal hydrophilic group
Internal olefin sulfonate
Risk assessment
Sustainable surfactant
Journal
Chemosphere
ISSN: 1879-1298
Titre abrégé: Chemosphere
Pays: England
ID NLM: 0320657
Informations de publication
Date de publication:
Jan 2022
Jan 2022
Historique:
received:
01
04
2021
revised:
11
07
2021
accepted:
23
07
2021
pubmed:
5
8
2021
medline:
11
11
2021
entrez:
4
8
2021
Statut:
ppublish
Résumé
Recently, a new sustainable anionic surfactant called bio-based internal olefin sulfonate (Bio IOS) has been developed. This surfactant enables excellent water solubility and high surface activity. It has a unique structure of long hydrophobic alkyl chains (C16 to C18) with two types of hydrophilic groups in its midsection, which distinguish it from other conventional anionic surfactants. However, the effects of the specific structural features of the surfactant on its environmental properties and the consequent effects on the environment remain unclear. In this study, we investigated the environmental fate and ecotoxicity of Bio IOS and the effects of the types and positions of hydrophilic groups on biodegradability and ecotoxicity. Biodegradation studies demonstrated that Bio IOS was readily biodegradable with >99.5% removal in wastewater treatment activated sludge (test concentration: 1 mg/L) and a fast half-life of 5.8 h in river water (test concentration: 10 μg/L); the excellent biodegradability was likely due to the high water solubility attributed to the internal hydrophilic groups. Meanwhile, moderately toxic effects were observed, whereby the 50% lethal and effect concentrations of the three freshwater species were above 1 mg/L. Ecotoxicity studies with different types and positions of hydrophilic groups revealed that hydroxyalkane sulfonate was less toxic and that toxicity was reduced in the presence of more internally located hydrophilic groups. These findings suggest that the hydroxyl group and the internal positions of hydrophilic groups that constitute the molecular configuration resembling two separate shorter alkyl chains may reduce the adverse effects on organisms despite the long alkyl chains.
Identifiants
pubmed: 34346340
pii: S0045-6535(21)02148-2
doi: 10.1016/j.chemosphere.2021.131676
pii:
doi:
Substances chimiques
Alkanesulfonates
0
Surface-Active Agents
0
Water Pollutants, Chemical
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
131676Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.