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The adsorption process of deionized water droplets on the parallel flow interface between ionic liquid [BMIM][PF6] and mineral oil is investigated in U-shaped microchannels. Three flow patterns of the efficient adsorption, moderate adsorption, and inefficient adsorption based on the adsorption efficiency were observed. The dimensionless droplet length D / W > 0.72 is conducive to efficient adsorption of droplets. When droplet shape factor β > 1, the lubrication pressure generated within the curved liquid film has a more significant hindrance on the adsorption process, and the reverse lubrication pressure at the outlet of the liquid film is the main reason for the rupture of the liquid film. An increase in the velocity of phase interface A-B movement can lead to an increase in lubrication pressure. A correlation model is established between the dimensionless adsorption length L * and the dimensionless adsorption time t *, and the influence of Laplace pressure is analyzed. [Display omitted] [ABSTRACT FROM AUTHOR]

2,4,6-trinitrophenol (TNP) has various industrial applications and is also extremely used by militaries and terrorists to make various explosives. Owing to their extensive industrial and military use and higher water solubility, their huge quantity is released into the environment and thus become a momentous environmental pollutant. TNP is highly toxic, poorly biodegradable, and a vigorous poison, strongly carcinogenic, and could cause severe diseases in humans and other animals. Thus, TNP present in the industrial wastewater and landfill leachate must be removed due to its detrimental effects on natural ecosystems. In the present review, the nature of TNP and its decontamination approaches are discussed, as well as their detailed mechanisms. The challenges that arise while applying TNP decontamination approaches were discussed and some future directions are highlighted for enhancing the efficiency of these approaches in a sustainable and friendly manner. [Display omitted] • Trinitrophenol (TNP) is a highly explosive and toxic pollutant, causing severe threats to human health and the environment. • Biodegradation, adsorption, photocatalytic degradation, and electrocatalytic degradation were employed to decontaminate TNP. • Incomplete biodegradation and secondary pollution generation in adsorption are the major challenges. • Photodegradation is a suitable treatment for complete remediation compared to conventional treatments. • Mechanistic understanding of the photodegradation of TNP via experimental and theoretical studies needs further exploration. [ABSTRACT FROM AUTHOR]

Various magnetic carbon materials have been employed for nuclide adsorption, yet there exists a research gap concerning their application in electro-adsorption for nuclide removal. In this study, a magnetic carbon nanotube nanocomposite (Fe 3 O 4 /CNT) was successfully synthesized as an electrode material through the hydrothermal method, involving the modification of minute Fe 3 O 4 nanoparticles onto the surface of carbon nanotubes (CNT). Electrochemical assessments revealed that the Fe 3 O 4 /CNT nanocomposite exhibited a higher specific capacitance compared to Fe 3 O 4 and CNT individually. The HRTEM image reveals a heterojunction structure formed directly between Fe 3 O 4 and CNT, which facilitates electron transmission. The Fe 3 O 4 /CNT nanocomposite was utilized as an electrode in a capacitive deionization (CDI) device for U (VI)-contaminated wastewater purification. Experimental results demonstrated that the maximum U (VI) adsorption capacity of the Fe 3 O 4 /CNT electrode reached 287.53 mg/g at 298 K, and the adsorption process conformed to the Langmuir isotherm model. Kinetic analysis further indicated that the adsorption of U (VI) by Fe 3 O 4 /CNT followed a pseudo-second-order kinetic model. Additionally, the Fe 3 O 4 /CNT nanocomposite was transformed into a flowable electrode liquid and applied in a flow-electrode capacitive deionization (FCDI) system for U (VI) removal from aqueous solutions. Leveraging its superparamagnetic properties, the Fe 3 O 4 /CNT flow-electrode within the FCDI system could be rapidly recovered via a straightforward magnetic separation procedure. Notably, after nine consecutive runs of the FCDI device, the Fe 3 O 4 /CNT flow-electrode successfully concentrated a low-concentration U (VI) solution of 120 mg/L into a high-concentration solution of 1230 mg/L, thereby achieving the goal of water resource conservation and reduced storage requirements. [Display omitted] • The high-performance Fe 3 O 4 /CNT nanocomposite was prepared through a one-pot method. • The Fe 3 O 4 /CNT has a higher specific capacitance because of the synergistic effect. • The Fe 3 O 4 /CNT can be used as an electrode for CDI and FCDI devices to remove U (VI). • The Fe 3 O 4 /CNT flow-electrode can be quickly recovered by magnetic separation. [ABSTRACT FROM AUTHOR]

• The continuous adsorptive removal of phenol using low-cost activated carbon was studied. • Effects of electromagnetic field (EMF), and electric potential (EP) in the phenol removal were studied. • EMF enhanced the removal performance of activated carbon electrodes on the aluminum substrate. In this study, we introduce an electrode configuration setup to study the effect of an electromagnetic field (EMF) and electric potential (EP) on phenol removal in a continuous adsorption process. Feed water contaminated with dissolved phenol was exposed to EMF and passed through charged activated carbon electrodes prepared from Phoenix dactylifera (palm tree) biowaste. This study investigated the effects of magnetic field exposure, electric potential, feed salinity, and electrode substrate type. The results revealed that the highest adsorption uptake capacity of 47.2 mg/g was achieved using an aluminum substrate (AS) with EMF at zero salinity. The phenol adsorption kinetics followed a pseudo-second-order adsorption rate and diffusion model, indicating that intraparticle diffusion was the primary rate-limiting mechanism. The increased phenol adsorption uptake capacity brought on by the EMF may result from the improved mass transfer and mobility of the adsorbate and, consequently, the increased effectiveness of the internal diffusion of the pollutants. Finally, a regeneration efficiency of 99 % was achieved using NaOH at a salinity of 5,000 ppm. [ABSTRACT FROM AUTHOR]