Development of novel experimental and modelled low density polyethylene (LDPE)-water partition coefficients for a range of hydrophobic organic compounds

Knowledge about partitioning constants of hydrophobic organic compounds (HOCs) between the polymer and aqueous phases is critical for assessing chemical environmental fate and transport. The conventional experimental method is characterized by large discrepancies in the measured values due to the limited water solubility of HOCs and other associated issues. In the current work, a novel three-phase partitioning system was evaluated to determine accurate low-density polyethylene (LDPE)-water partition coefficients (KPE-w). By adding sufficient surfactant (Brij 30) to form the micellar pseudo-phase within the polymer/water system, the KPE-w values were obtained from a combination of two experimentally measured values, that is, the micelle-water partition coefficient (Kmic-w) and the LDPE-micelle partition coefficient (KPE-mic). The method presented here is capable of shortening the equilibration time to half a month, and avoiding defects of the traditional method with respect to directly measured aqueous phase concentrations. Herein, the KPE-w values were determined for HOCs with little errors. Meanwhile, based on the 120 experimental KPE-w data, several in silico models were also developed as valid extrapolation tools to estimate missing or uncertain values. Analysis of the underlying solubility interactions in the nonionic surfactant micelles were investigated, providing additional support for the reliability of the proposed method.

Automated summary

The novel three-phase partitioning system using surfactant to form micellar pseudo-phase successfully determined the partition coefficient between LDPE and water, avoiding the limitations of direct measurement of aqueous phase concentrations. Through 120 experimental data and in silico models, estimation of missing or uncertain values was achieved, enhancing the accuracy of KPE-w values.