Quantification of Bulk Solution Limits for Liquid and Interfacial Transport in Nanoconfinements

Langmuir ◽  
2015 ◽  
Vol 31 (7) ◽  
pp. 2167-2179 ◽  
Author(s):  
Shaina Kelly ◽  
Matthew T. Balhoff ◽  
Carlos Torres-Verdín
Keyword(s):  
Bulk Solution ◽  
Interfacial Transport

Theoretical analysis of counter-current absorption of a poorly soluble gas based on the PDE-AD model

1986 ◽  
Vol 51 (6) ◽  
pp. 1222-1239 ◽  
Author(s):  
Pavel Moravec ◽  
Vladimír Staněk
Keyword(s):  
Experimental Data ◽  
Liquid Phase ◽  
Gas Phase ◽  
Transfer Functions ◽  
Packed Bed ◽  
Packed Bed Column ◽  
Interfacial Transport ◽  
Gaseous Component ◽  
Poorly Soluble ◽  
Counter Current

Expression have been derived in the paper for all four possible transfer functions between the inlet and the outlet gas and liquid steams under the counter-current absorption of a poorly soluble gas in a packed bed column. The transfer functions have been derived for the axially dispersed model with stagnant zone in the liquid phase and the axially dispersed model for the gas phase with interfacial transport of a gaseous component (PDE - AD). calculations with practical values of parameters suggest that only two of these transfer functions are applicable for experimental data evaluation.

Analysis of observability of model parameters for physical absorption of poorly soluble gases in packed beds

1982 ◽  
Vol 47 (10) ◽  
pp. 2639-2653 ◽  
Author(s):  
Pavel Moravec ◽  
Vladimír Staněk
Keyword(s):  
Transfer Functions ◽  
Plug Flow ◽  
Packed Bed ◽  
Model Parameters ◽  
Packed Bed Column ◽  
Interfacial Transport ◽  
Complex Arithmetic ◽  
Physical Absorption ◽  
Poorly Soluble ◽  
Phase Lags

Expressions have been derived for four possible transfer functions of a model of physical absorption of a poorly soluble gas in a packed bed column. The model has been based on axially dispersed flow of gas, plug flow of liquid through stagnant and dynamic regions and interfacial transport of the absorbed component. The obtained transfer functions have been transformed into the frequency domain and their amplitude ratios and phase lags have been evaluated using the complex arithmetic feature of the EC-1033 computer. Two of the derived transfer functions have been found directly applicable for processing of experimental data. Of the remaining two one is useable with the limitations to absorption on a shallow layer of packing, the other is entirely worthless for the case of poorly soluble gases.

scholarly journals Efficacy of a Phosphate-Charged Soil Material in Supplying Phosphate for Plant Growth in Soilless Root Media

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Young-Mi Oh ◽  
Paul V. Nelson ◽  
Dean L. Hesterberg ◽  
Carl E. Niedziela
Keyword(s):  
Plant Growth ◽  
Solution Concentration ◽  
Bulk Solution ◽  
P Deficiency ◽  
Soil Material ◽  
Hydrous Oxides ◽  
Acceptable Range ◽  
Root Media ◽  
Phosphate Fertilization ◽  
Phosphate Leaching

A soil material high in crystalline Fe hydrous oxides and noncrystalline Al hydrous oxides collected from the Bw horizon of a Hemcross soil containing allophane from the state of Oregon was charged with phosphate-P at rates of 0, 2.2, and 6.5 mg·g−1, added to a soilless root medium at 5% and 10% by volume, and evaluated for its potential to supply phosphate at a low, stable concentration during 14 weeks of tomato (Solanum esculentumL.) seedling growth. Incorporation of the soil material improved pH stability, whether it was charged with phosphate or not. Bulk solution phosphate-P concentrations in the range of 0.13 to 0.34 mg·dm−3were associated with P deficiency. The only treatment that sustained an adequate bulk solution concentration of phosphate-P above 0.34 mg·dm−3for the 14 weeks of testing contained 10% soil material charged with 6.5 mg·g−1P, but initial dissolved P concentrations were too high (>5 mg·g−1phosphate-P) from the standpoint of phosphate leaching. The treatment amended with 10% soil material charged with 2.2 mg·g−1P maintained phosphate-P within an acceptable range of 0.4 to 2.3 mg·dm−3for 48 d in a medium receiving no postplant phosphate fertilization.

scholarly journals The Additive Influence of Propane-1,2-Diol on SDS Micellar Structure and Properties

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3773
Author(s):  
Martina Gudelj ◽  
Paola Šurina ◽  
Lucija Jurko ◽  
Ante Prkić ◽  
Perica Bošković
Keyword(s):  
Mixed Solvents ◽  
Sodium Dodecyl ◽  
Shielding Effect ◽  
Bulk Solution ◽  
Structure And Properties ◽  
Micellar Structure ◽  
Related Substances ◽  
Micellar Systems ◽  
Small Change ◽  
Additive Influence

Micellar systems are colloids with significant properties for pharmaceutical and food applications. They can be used to formulate thermodynamically stable mixtures to solubilize hydrophobic food-related substances. Furthermore, micellar formation is a complex process in which a variety of intermolecular interactions determine the course of formation and most important are the hydrophobic and hydrophilic interactions between surfactant–solvent and solvent–solvent. Glycols are organic compounds that belong to the group of alcohols. Among them, propane-1,2-diol (PG) is a substance commonly used as a food additive or ingredient in many cosmetic and hygiene products. The nature of the additive influences the micellar structure and properties of sodium dodecyl sulfate (SDS). When increasing the mass fraction of propane-1,2-diol in binary mixtures, the c.m.c. values decrease because propane-1,2-diol is a polar solvent, which gives it the ability to form hydrogen bonds, decreasing the cohesivity of water and reducing the dielectric constant of the aqueous phase. The values of ΔGm0 are negative in all mixed solvents according to the reduction in solvophobic interactions and increase in electrostatic interaction. With the rising concentration of cosolvent, the equilibrium between cosolvent in bulk solution and in the formed micelles is on the side of micelles, leading to the formation of micelles at a lower concentration with a small change in micellar size. According to the 1H NMR, with the addition of propylene glycol, there is a slight shift of SDS peaks towards lower ppm regions in comparison to the D2O peak. The shift is more evident with the increase in the amount of added propane-1,2-diol in comparison to the NMR spectra of pure SDS. Addition of propane-1,2-diol causes the upfield shift of the protons associated with hydrophilic groups, causing the shielding effect. This signifies that the alcohol is linked with the polar head groups of SDS due to its proximity to the SDS molecules.

scholarly journals The influence of active carbon contaminants on the ozonation mechanism interpretation

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lilla Fijołek ◽  
Joanna Świetlik ◽  
Marcin Frankowski
Keyword(s):  
Activated Carbon ◽  
Active Carbon ◽  
Alkali Metals ◽  
Activated Carbons ◽  
Carbon Surface ◽  
Bulk Solution ◽  
Ozone Decomposition ◽  
Reaction Products ◽  
Treatment Technology ◽  
Carbon Impurities

AbstractIn water treatment technology, activated carbons are used primarily as sorbents to remove organic impurities, mainly natural organic matter, but also as catalysts in the ozonation process. Commercially available activated carbons are usually contaminated with mineral substances, classified into two main groups: alkali metals (Ca, Na, K, Li, Mg) and multivalent metals (Al, Fe, Ti, Si). The presence of impurities on the carbon surface significantly affects the pHpzc values determined for raw and ozonated carbon as well as their acidity and alkalinity. The scale of the observed changes strongly depends on the pH of the ozonated system, which is related to the diffusion of impurities from the carbon to the solution. In an acidic environment (pH 2.5 in this work), the ozone molecule is relatively stable, yet active carbon causes its decomposition. This is the first report that indirectly indicates that contaminants on the surface of activated carbon (multivalent elements) contribute to the breakdown of ozone towards radicals, while the process of ozone decomposition by purified carbons does not follow the radical path in bulk solution. Carbon impurities also change the distribution of the reaction products formed by organic pollutants ozonation, which additionally confirms the radical process. The study showed that the use of unpurified activated carbon in the ozonation of succinic acid (SA) leads to the formation of a relatively large amount of oxalic acid (OA), which is a product of radical SA degradation. On the other hand, in solutions with purified carbon, the amount of OA generated is negligible.

Living polymerizations of propylene sulfide initiated with potassium xanthates characterized by unprecedentedly high propagation rates

2021 ◽  
Author(s):  
Misha Rumyantsev
Keyword(s):  
Bulk Solution ◽  
Living Polymerizations

In this paper we describe the original thiol-free approach towards the polymerization of propylene sulfide (PS) under various conditions (bulk, solution, and emulsion) initiated with potassium xanthates.

scholarly journals A Review on Recent Progress of Glycan-Based Surfactant Micelles as Nanoreactor Systems for Chemical Synthesis Applications

2021 ◽  
Vol 2 (1) ◽  
pp. 168-186
Author(s):  
Bahareh Vafakish ◽  
Lee D. Wilson
Keyword(s):  
Chemical Synthesis ◽  
Chemical Reactions ◽  
Recent Progress ◽  
Chemical Species ◽  
Reaction Rates ◽  
Bulk Solution ◽  
Surfactant Micelles ◽  
Conventional Surfactant ◽  
Recent Developments ◽  
To Receive

The nanoreactor concept and its application as a modality to carry out chemical reactions in confined and compartmentalized structures continues to receive increasing attention. Micelle-based nanoreactors derived from various classes of surfactant demonstrate outstanding potential for chemical synthesis. Polysaccharide (glycan-based) surfactants are an emerging class of biodegradable, non-toxic, and sustainable alternatives over conventional surfactant systems. The unique structure of glycan-based surfactants and their micellar structures provide a nanoenvironment that differs from that of the bulk solution, and supported by chemical reactions with uniquely different reaction rates and mechanisms. In this review, the aggregation of glycan-based surfactants to afford micelles and their utility for the synthesis of selected classes of reactions by the nanoreactor technique is discussed. Glycan-based surfactants are ecofriendly and promising surfactants over conventional synthetic analogues. This contribution aims to highlight recent developments in the field of glycan-based surfactants that are relevant to nanoreactors, along with future opportunities for research. In turn, coverage of research for glycan-based surfactants in nanoreactor assemblies with tailored volume and functionality is anticipated to motivate advanced research for the synthesis of diverse chemical species.

scholarly journals Single entity electrochemistry and the electron transfer kinetics of hydrazine oxidation

Nano Research ◽  
2021 ◽  
Author(s):  
Ruiyang Miao ◽  
Lidong Shao ◽  
Richard G. Compton
Keyword(s):  
Electron Transfer ◽  
Bulk Solution ◽  
Relative Contribution ◽  
Rate Determining Step ◽  
Multistep Process ◽  
Ph Range ◽  
Electro Catalytic Oxidation ◽  
Single Particle Impact ◽  
The Impact ◽  
Kinetics Of

AbstractThe mechanism and kinetics of the electro-catalytic oxidation of hydrazine by graphene oxide platelets randomly decorated with palladium nanoparticles are deduced using single particle impact electrochemical measurements in buffered aqueous solutions across the pH range 2–11. Both hydrazine, N2H4, and protonated hydrazine N2H5+ are shown to be electroactive following Butler-Volmer kinetics, of which the relative contribution is strongly pH-dependent. The negligible interconversion between N2H4 and N2H5+ due to the sufficiently short timescale of the impact voltammetry, allows the analysis of the two electron transfer rates from impact signals thus reflecting the composition of the bulk solution at the pH in question. In this way the rate determining step in the oxidation of each specie is deduced to be a one electron step in which no protons are released and so likely corresponds to the initial formation of a very short-lived radical cation either in solution or adsorbed on the platelet. Overall the work establishes a generic method for the elucidation of the rate determining electron transfer in a multistep process free from any complexity imposed by preceding or following chemical reactions which occur on the timescale of conventional voltammetry.

scholarly journals A Two-Scale Computational Model of pH-Sensitive Expansive Porous Media

2013 ◽  
Vol 80 (2) ◽  
Author(s):  
Ranena V. Ponce F. ◽  
Márcio A. Murad ◽  
Sidarta A. Lima
Keyword(s):  
Electrolyte Solution ◽  
Solid Phase ◽  
Scale Model ◽  
Bulk Solution ◽  
Neumann Condition ◽  
Pore Scale ◽  
Exchange Reactions ◽  
Layer Potential ◽  
Bulk Fluid ◽  
Monovalent Ions

We propose a new two-scale model to compute the swelling pressure in colloidal systems with microstructure sensitive to pH changes from an outer bulk fluid in thermodynamic equilibrium with the electrolyte solution in the nanopores. The model is based on establishing the microscopic pore scale governing equations for a biphasic porous medium composed of surface charged macromolecules saturated by the aqueous electrolyte solution containing four monovalent ions (Na+,Cl-,H+,OH-). Ion exchange reactions occur at the surface of the particles leading to a pH-dependent surface charge density, giving rise to a nonlinear Neumann condition for the Poisson–Boltzmann problem for the electric double layer potential. The homogenization procedure, based on formal matched asymptotic expansions, is applied to up-scale the pore-scale model to the macroscale. Modified forms of Terzaghi's effective stress principle and mass balance of the solid phase, including a disjoining stress tensor and electrochemical compressibility, are rigorously derived from the upscaling procedure. New constitutive laws are constructed for these quantities incorporating the pH-dependency. The two-scale model is discretized by the finite element method and applied to numerically simulate a free swelling experiment induced by chemical stimulation of the external bulk solution.

Aggregation Behaviours of Surface-Active Ionic Liquids 1-Alkyl-3-methylimidazolium Bis(2-ethylhexyl)sulfosuccinate

2016 ◽  
Vol 69 (11) ◽  
pp. 1254 ◽  
Author(s):  
Jiequn Wu ◽  
Tianxiang Yin ◽  
Shaoxiong Shi ◽  
Weiguo Shen
Keyword(s):  
Ionic Liquids ◽  
Self Assembly ◽  
Alkyl Chain ◽  
Systematic Investigation ◽  
Bulk Solution ◽  
Free Energies ◽  
Imidazolium Cation ◽  
Structure Transition ◽  
Surface Active ◽  
Counter Ion Binding

The systematic investigation of the aggregation behaviours of newly synthesised surface-active ionic liquids 1-alkyl-3-methylimidazolium bis(2-ethylhexyl)sulfosuccinate ([Cnmim][AOT], n = 2, 3, 5, 6, 7) by various techniques is reported. The critical aggregation concentrations (CACs) and the standard Gibbs free energies of aggregation () were determined from measurements on conductivity, fluorescence, and surface tension, which suggested a stronger self-assembly ability in the bulk solution for [Cnmim][AOT] surfactants with longer alkyl chain cations. An interesting structure transition driven by the penetration of the imidazolium cation into the aggregate when n > 4 was found by analysis of the variations of the values of CAC, , the degree of counter ion binding (β), and the micropolarity (I1/I3) immediately after the CAC with changing alkyl chain length of the imidazolium cation, which was further confirmed by 1H NMR measurements.

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