Photochemical transformation of liquid crystal monomers in simulated environmental media: Kinetics, mechanism, toxicity variation and QSAR modeling

• Published in: Water research (Oxford) 2024-09, Vol.261, p.122062, Article 122062
• Main Authors: Yang, Yandong, Jiang, Xiangkun, Yang, Yi, Wang, Jia, Zhao, Yahui, Lin, Shanshan, Qu, Jiao, Martyniuk, Christopher J., Zhao, Yuanhui, Li, Chao
• Format: Article
• Language: English
• Subjects: Computational simulation; LCMs; Leaf wax model; Photodegradation; QSAR; Toxicity assessment
• ISSN: 0043-1354; 1879-2448; 1879-2448
• DOI: 10.1016/j.watres.2024.122062

•The photolysis rate order is biphenylethynes > phenylbenzoates > di/terphenyl LCMs.•The phenylbenzoate and biphenylethyne LCMs mainly undergo direct photolysis.•The di/terphenyl LCMs mainly undergo self-sensitized photolysis.•Most photolysis products remain toxic to aquatic organisms to some degree.•Two QSAR models for predicting kobs of LCMs on leaf wax models are developed. Liquid crystal monomers (LCMs) are a new class of emerging pollutants with high octanol-water partition coefficients; however, their transformation behavior and associated risk to environments with high organic matter content has rarely been reported. In this study, we investigated the photodegradation kinetics, mechanism, and toxicity variation of 23 LCMs on leaf wax models (e.g., organic solvents methanol and n-hexane). The order of the photolysis rates of these LCMs were biphenylethyne LCMs > phenylbenzoate LCMs > diphenyl/terphenyl LCMs under simulated sunlight, while the phenylcyclohexane LCMs were resistant to photodegradation. The phenylbenzoate and biphenylethyne LCMs mainly undergo direct photolysis, while the diphenyl/terphenyl LCMs mainly undergo self-sensitized photolysis. The main photolysis pathways are the cleavage of ester bonds for phenylbenzoate LCMs, the addition, oxidation and cleavage of alkynyl groups for biphenylethyne LCMs, and the cleavage/oxidation of chains attached to phenyls and the benzene ring opening for diphenyl/terphenyls LCMs. Most photolysis products remained toxic to aquatic organisms to some degree. Additionally, two quantitative structure-activity relationship models for predicting kobs of LCMs in methanol and n-hexane were developed, and employed to predict kobs of 93 LCMs to fill the kobs data gap in systems mimicking leaf surfaces. These results can be helpful for evaluating the fate and risk of LCMs in environments with high content of organic phase. [Display omitted]