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重新审视描述多种化学物质在聚乙烯水被动采样器中分配行为的线性自由能关系。

Relook on the Linear Free Energy Relationships Describing the Partitioning Behavior of Diverse Chemicals for Polyethylene Water Passive Samplers.

作者信息

Khawar Muhammad Irfan, Nabi Deedar

机构信息

Institute of Environmental Sciences and Engineering (IESE), National University of Sciences and Technology (NUST), H-12, Islamabad 48000, Pakistan.

Bigelow Laboratory for Ocean Sciences, 60 Bigelow Dr, East Boothbay, Maine 04544, United States.

出版信息

ACS Omega. 2021 Feb 12;6(8):5221-5232. doi: 10.1021/acsomega.0c05179. eCollection 2021 Mar 2.

Abstract

Over the past 3 decades, low-density polyethylene (PE) passive sampling devices have been widely used to scout organic chemicals in air, water, sediments, and biotic phases. Experimental partition coefficient data, required to calculate the concentrations in environmental compartments, are not widely available. In this study, we developed and rigorously evaluated linear free energy relationships (LFERs) to predict the partition coefficient between the PE and the water phase (log ). Poly-parameter (pp) LFERs based on Abraham solute parameters performed better (root-mean-square error, rmse = 0.333-0.350 log unit) in predicting log compared to the two one-parameter (op) LFERs built on -hexadecane-water and octanol-water partition coefficients (rmse = 0.41-0.42 log unit), indicating that one parameter is not able to account for all types of interactions experienced by a chemical during PE-water exchange. Dimensionality analyses show that the calibration dataset used to train pp-LFERs fulfills all the requirements to obtain a robust model for log . Van der Waals interactions of the molecule tend to favor the PE phase, and polar interactions of the molecule favor the water phase. The PE phase is the most sensitive to polarizable chemicals compared to other commonly used passive sampling polymeric phases such as polydimethylsiloxane, polyoxymethylene, and polyacrylate. For op-LFERs, the PE phase is better represented by the hexadecane phase than by the octanol phase. A computational method based on the conductor-like screening model for real solvents theory did good job in estimating log for chemicals that were neither very hydrophobic nor very hydrophilic in nature. Our models can be used to reliably predict the log values of simple neutral organic chemicals. This study provides insights into the partitioning behavior of PE samplers compared to other commonly used passive samplers.

摘要

在过去30年中,低密度聚乙烯(PE)被动采样装置已被广泛用于探测空气、水、沉积物和生物相中 的有机化学品。计算环境介质中浓度所需的实验分配系数数据并不广泛可得。在本研究中,我们开发并严格评估了线性自由能关系(LFERs),以预测PE与水相之间的分配系数(log )。与基于正十六烷 - 水和辛醇 - 水分配系数建立的两个单参数(op)LFERs(均方根误差,rmse = 0.41 - 0.42对数单位)相比,基于亚伯拉罕溶质参数的多参数(pp)LFERs在预测log 方面表现更好(rmse = 0.333 - 0.350对数单位),这表明单一参数无法解释化学品在PE - 水交换过程中经历的所有类型的相互作用。维度分析表明,用于训练pp - LFERs的校准数据集满足获得log 稳健模型的所有要求。分子的范德华相互作用倾向于有利于PE相,而分子的极性相互作用有利于水相。与其他常用的被动采样聚合物相(如聚二甲基硅氧烷、聚甲醛和聚丙烯酸酯)相比,PE相对可极化化学品最为敏感。对于op - LFERs,用正十六烷相比用辛醇相能更好地代表PE相。基于导体类筛选模型的真实溶剂理论的计算方法在估算性质既不太疏水也不太亲水的化学品的log 方面表现良好。我们的模型可用于可靠地预测简单中性有机化学品的log 值。本研究深入探讨了PE采样器与其他常用被动采样器相比的分配行为。

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