Practical designs of non-aqueous phase liquids (NAPLs) remediation strategies require reliable modeling of interphase mass transfer to predict the retraction of NAPL during processes such as dissolution. In this work, the dissolution process of NAPL during two-phase flow in heterogeneous porous media is studied using pore-network modeling and micromodel experiments. A new physical-experimental approach is proposed to enhance the prediction of the dissolution process during modeling of interphase mass transfer. In this regard, the normalized average resident solute concentration is evaluated for describing the dissolution process at pore-level. To incorporate the effect of medium heterogeneities, a new experimental factor is considered for enhancing corner diffusion modeling. In addition, capillary desaturation curves (CDCs) are predicted during hydraulic flow modeling to estimate initial residual NAPL saturation. The developed network model can predict residual NAPL saturations and mass transfer rate coefficient for a NAPL-water system at different injection rates and fluid saturations. The evaluated mass transfer rate coefficients using the proposed physical-experimental approach show a significant improvement compared to either mechanistic or empirical methods. The proposed approach in this study can be attractive for possible applications in commercial simulators of contaminant transport in porous media.
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http://dx.doi.org/10.1016/j.jconhyd.2019.103565 | DOI Listing |
Nano Lett
January 2025
Institut Charles Sadron, Université de Strasbourg and CNRS, 67034 Strasbourg, France.
Anisometric plasmonic nanoparticles find applications in various fields, from photocatalysis to biosensing. However, exposure to heat or to specific chemical environments can induce their reshaping, leading to loss of function. Understanding this process is therefore relevant both for the fundamental understanding of such nano-objects and for their practical applications.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Zhejiang University, College of Chemical and Biological Engineering, CHINA.
Electrochemical water splitting is a pivotal technology for storing intermittent electricity from renewable sources into hydrogen fuel. However, its overall energy efficiency is impeded by the sluggish oxygen evolution reaction (OER) at the anode. In the quest to design high-performance anode catalysts for driving the OER under non-acidic conditions, iron (Fe) has emerged as a crucial element.
View Article and Find Full Text PDFChemistry
January 2025
Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospekt 47, 119991, Moscow, RUSSIAN FEDERATION.
Palladium catalysts form a cornerstone of modern chemistry with upmost scientific and industrial impact. Bulk palladium metal itself is chemically inert, and a sequence of chemical transformations has to be utilized to convert the metal into Pd pre-catalyst covered by ligands. However, the "cocktail" of catalysis concept discovered recently has shown that Pd systems can efficiently operate in catalysis without the necessity of a complicated and expensive pre-installed ligand environment.
View Article and Find Full Text PDFRecent Pat Nanotechnol
January 2025
Raj Kumar Goel Institute of Technology (Pharmacy), 5-Km. Stone, Delhi-Meerut Road, Ghaziabad, Uttar Pradesh, India.
Background: Nanosuspension has emerged as an effective, lucrative, and unequalled approach for efficiently elevating the dissolution and bioavailability of aqueous soluble drugs. Diverse challenges persist within this domain, demanding further comprehensive investigation and exploration.
Objective: This study aims to design, develop, optimise formulation and process variables, and characterise the stabilised aqueous dissolvable nanosuspension using chlorthalidone as a BCS class- IV drug.
Chem Commun (Camb)
January 2025
State Key Laboratory of Electronic Thin Film and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054, China.
Metallic vanadium is innovatively introduced for a superior aqueous zinc-ion battery cathode material, which is activated through dissolution-deposition transition to amorphous VO·3HO and delivers an excellent capacity of 610 mA h g at 0.1 A g and remarkable capacity retention rate of 80.3% after 1000 cycles at 1 A g.
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