Sorption and desorption behaviors of triphenyl phosphate (TPhP) and its degradation intermediates on aquatic sediments.

As triphenyl phosphate (TPhP) can biodegrade extensively in sediments, researches should further the understanding of the fate and transport of TPhP and its degradation intermediates in the environment. Therefore, the sorption/desorption behaviors of TPhP, diphenyl phosphate (DPhP) and phenyl phosphate (PhP) on sediments were investigated. The kinetic process was well-fitted by pseudo-second-order model, suggesting that chemisorption was involved. And the Langmuir model could describe the sorption isotherms of TPhP and DPhP well except for PhP. The redundancy analysis revealed that the sorption amount had a positive correlation with sediment organic matter, zeta potential and C/H of sediments. Besides the sorption/desorption behaviors were greatly influenced by the physicochemical properties of the sorbates. PhP with high molecular electrostatic potential (0.132 e0) was prone to protonation and formed hydrogen bonds, leading to higher sorption. Furthermore, hydrophobicity, π-π interactions, Lewis acid-base interaction and hydrogen bonding were involved in the sorption process and resulted in nonlinear sorption isotherms. TPhP, DPhP and PhP exhibited apparent desorption hysteresis on the sediments. Sediments with organic matter removed, which have complex pore distributions, exhibited more hysteresis. These results may contribute to the risk assessment and fate modeling of TPhP and its degradation products in sediments.