Interfacial Mass Transfer in Trichloroethylene/Surfactants/ Water Systems: Implications for Remediation Strategies

The fate of dense non-aqueous phase liquids (DNAPLs) in the environment and the consequential remediation problems have been intensively studied over the last 50 years. However, a scarce literature is present about the mass transfer at the DNAPL/water interface. In this paper, we present a fast method for the evaluation of the mass transfer performance of a surfactant that can easily be employed to support an effective choice for the so-called enhanced remediation strategies. We developed a lab-scale experimental system modelled by means of simple ordinary differential equations to calculate the mass transfer coefficient (K) of trichloroethylene, chosen as representative DNAPL, in the presence and in the absence of two ethoxylated alcohols belonging to the general class of Synperonic surfactants. Our findings revealed that it exists an optimal surfactant concentration range, where K increases up to 40% with respect to pure water.

In-situ plasmonic tracking oxygen evolution reveals multistage oxygen diffusion and accumulating inhibition

Understanding mass transfer processes concomitant with electrochemical conversion for gas evolution reactions at the electrode-electrolyte interface plays a key role in advancing renewable energy storage and conversion. However, due to the complicated diffusion behavior of gas at the dynamic catalytic interfaces, it is still a great challenge to accurately portray mass transfer of gas during electrocatalysis process. Here, we track the diffusion of dissolved oxygen on Cu nanostructured plasmonic interface, which reveals multistage oxygen diffusion behaviors, including premature oxygen accumulation, spontaneous diffusion and accelerated oxygen dissipation. This work uncovers an accumulating inhibition effect on oxygen evolution arising from interfacial dissolved oxygen. With these knowledges, we develop a programmable potential scan strategy to eliminate interfacial gas products, which alleviates the concentration polarization, releases accessible actives sites and promotes electrocatalytic performance. Our findings provide a direct observation of the interfacial mass transfer processes that governs the kinetics of gas-involved multiphases catalysis.