Trisiloxane ethoxylates (TSEOn) have been found in multiple agro-environmental media due to their pervasive application in agricultural production. While some studies suggested that the differences in the toxicological effects of TSEOn were closely related to their end-capping groups, the environmental behaviors and fate of TSEOn congeners with varying end-capping groups in agroecosystems remain underexplored. This study investigated the dissipation patterns of 39 oligomers across three TSEOn congeners in cucumber, leaves, and soils through field trials, including TSEOn-H (hydroxy, n = 2-14), TSEOn-CH (methoxy, n = 2-14), and TSEOn-COCH (acetoxy, n = 3-15). All TSEOn oligomers dissipated following pseudo-first-order kinetics in cucumber, leaves, and soils with half-lives were 2.08-3.92 d, 1.77-4.44 d, and 5.06-19.80 d, respectively. TSEOn congeners in agro-environmental media presented different dissipation patterns affected by their end-capping groups. The interfacial behaviors of TSEOn-COCH in the leaves differed from those of TSEOn-H and TSEOn-CH. The half-lives of TSEOn-H and TSEOn-CH congeners in soils were significantly positively correlated with log K, indicating that long-chain congeners preferentially partition to soil solid phases, leading to slower dissipation rates than short-chain congeners. Furthermore, long-chain TSEOn congeners may dissipate to short-chain congeners. The dietary risks of ΣTSEOn-CH intake through cucumber fruits were deemed safe for different Chinese populations based on the margin of exposure (MOE) assessment. This study alerts us to the environmental behaviors and fate of organosilicone surfactants and provides a baseline reference to the dietary exposure risks of TSEOn.
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http://dx.doi.org/10.1016/j.jhazmat.2025.137167 | DOI Listing |
J Hazard Mater
January 2025
Key Laboratory of Agro-product Quality and Safety, Institute of Quality Standards & Testing Technology for Agro-products, Chinese Academy of Agricultural Sciences, Beijing 100081, China. Electronic address:
Trisiloxane ethoxylates (TSEOn) have been found in multiple agro-environmental media due to their pervasive application in agricultural production. While some studies suggested that the differences in the toxicological effects of TSEOn were closely related to their end-capping groups, the environmental behaviors and fate of TSEOn congeners with varying end-capping groups in agroecosystems remain underexplored. This study investigated the dissipation patterns of 39 oligomers across three TSEOn congeners in cucumber, leaves, and soils through field trials, including TSEOn-H (hydroxy, n = 2-14), TSEOn-CH (methoxy, n = 2-14), and TSEOn-COCH (acetoxy, n = 3-15).
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November 2024
Department of Mechanical and Aerospace Engineering, Politecnico di Torino, 10129 Turin, Italy.
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College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
Transfus Med Hemother
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Department of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Angew Chem Int Ed Engl
December 2024
School of Chemistry, Beihang University, Beijing, 100191, P. R. China.
The strategy of isomerization is known for its simple yet effective role in optimizing molecular configuration and enhancing the power conversion efficiency (PCE) of organic solar cells (OSCs). However, the impact of isomerization on the design of dimer acceptors has been rarely investigated, and the relationship between the chemical structure and optoelectronic property remains unclear. In this study, we designed and synthesized two dimer acceptor isomers named D-TPh and D-TN, which differ in the positional arrangement of their end capping groups.
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