BLBinlong Liu

Binlong Liu

*This is an algorithmically generated author record based on publicly available information.

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Binlong Liu has a total of 4 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Passive sampling of polycyclic aromatic hydrocarbons with low-density polyethylene: Equilibration limitations in aqueous suspensions

    by Jialin Liu, Binlong Liu, Shuya Xie, Peter Grathwohl

    Polyethylene (PE) and other polymers are widely and successfully used as passive samplers for organic pollutants in the environment. This study provides high-resolution experimental data from batch shaking tests on the uptake, reversibility, and linear equilibrium partitioning of polycyclic aromatic hydrocarbons (PAHs) using two different PE sheets of 30 µm and 80 µm thickness. Kinetics for phenanthrene are well described by a mechanistic first-order model with mass transfer limited by an aqueous boundary layer (with a mean thickness of 170 µm). Equilibration in laboratory batch systems during uptake and desorption is very rapid with characteristic times of 1–2 h but this depends on the boundary condition, e.g., the ratio of PE mass to water volume. Therefore, equilibration of PE in other setups, e.g., in soil slurries or sediment suspensions, may take orders of magnitude longer because the boundary condition for PE changes from finite to infinite bath conditions (soil or sediment particles may keep the concentration in water almost constant). Solid precipitates for high molecular weight PAHs explain partition coefficients below expected values because of kinetic limitations in such a system. Nevertheless, passive sampling can be employed safely if such limitations are considered; furthermore, partition coefficients can be estimated accurately by empirical relationships (e.g., within 0.1 log unit) based on molecular weight, octanol/water partition coefficients, or subcooled liquid solubilities.


  • Open Access

    Mass Transfer Principles in Column Percolation Tests: Initial Conditions and Tailing in Heterogeneous Materials

    by Binlong Liu, Michael Finkel, Peter Grathwohl

    Initial conditions (pre-equilibrium or after the first flooding of the column), mass transfer mechanisms and sample composition (heterogeneity) have a strong impact on leaching of less and strongly sorbing compounds in column percolation tests. Mechanistic models as used in this study provide the necessary insight to understand the complexity of column leaching tests especially when heterogeneous samples are concerned. By means of numerical experiments, we illustrate the initial concentration distribution inside the column after the first flooding and how this impacts leaching concentrations. Steep concentration gradients close to the outlet of the column have to be expected for small distribution coefficients (Kd<1 L kg−1) and longitudinal dispersion leads to smaller initial concentrations than expected under equilibrium conditions. In order to elucidate the impact of different mass transfer mechanisms, film diffusion across an external aqueous boundary layer (first order kinetics, FD) and intraparticle pore diffusion (IPD) are considered. The results show that IPD results in slow desorption kinetics due to retarded transport within the tortuous intragranular pores. Non-linear sorption has not much of an effect if compared to Kd values calculated for the appropriate concentration range (e.g., the initial equilibrium concentration). Sample heterogeneity in terms of grain size and different fractions of sorptive particles in the sample have a strong impact on leaching curves. A small fraction (<1%) of strongly sorbing particles (high Kd) carrying the contaminant may lead to very slow desorption rates (because of less surface area)—especially if mass release is limited by IPD—and thus non-equilibrium. In contrast, mixtures of less sorbing fine material (“labile” contamination with low Kd), with a small fraction of coarse particles carrying the contaminant leads to leaching close to or at equilibrium showing a step-wise concentration decline in the column effluent.