Penetration Parameter for an Adsorbed Layer of Polarizable Ions

1966 ◽  
Vol 37 (9) ◽  
pp. 3471-3482 ◽  
Author(s):  
J. Ross MacDonald ◽  
C. A. Barlow
Keyword(s):  
Adsorbed Layer ◽  
Penetration Parameter

Adsorption and Oxidation of Thiosulfate on the Platinum Electrode in a Slightly Alkaline Medium

2000 ◽  
Vol 65 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Tomáš Loučka
Keyword(s):  
Alkaline Medium ◽  
Oxidation Reaction ◽  
Open Circuit Potential ◽  
Platinum Electrode ◽  
Adsorbed Layer ◽  
Open Circuit ◽  
Adsorbed Hydrogen ◽  
Oxidation Number ◽  
Hydrogen Electrode ◽  
Layer Region

The aim of this research was to study the oxidation and reduction of the adsorbed thiosulfate on the platinum electrode in a slightly alkaline medium. The adsorption was performed at the open circuit conditions. The reduction of the adsorbed layer in the hydrogen region is slower in a slightly alkaline medium than in acid. The mechanism of reduction and oxidation of adsorbed molecules is probably the same. The nonstationary currents measured in presence of thiosulfates showed that the change in the oxidation number does not take place during the adsorption in the double layer region. In the hydrogen region, thiosulfate replaces the adsorbed hydrogen while beeing reduced. Nonstationary currents at higher concentrations of thiosulfate indicate the presence of more layers on the electrode. Upon reaching higher concentrations of thiosulfate the oxidation reaction takes place between thiosulfate in solution and adsorbed product of its reduction. The open circuit potential of the platinum electrode measured in a thiosulfate solution was 0.780 and 0.783 V against the hydrogen electrode in the same solution.

scholarly journals Computer Analysis of the Porous Structure of Activated Carbons Derived from Various Biomass Materials by Chemical Activation

Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4121
Author(s):  
Mirosław Kwiatkowski ◽  
Elżbieta Broniek
Keyword(s):  
Porous Structure ◽  
Adsorption Isotherms ◽  
Computer Analysis ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Adsorbed Layer ◽  
Dry Mass ◽  
Mass Ratio ◽  
Adsorption Volume ◽  
Homogeneous Surface

In this study, the preparation of activated carbons from various materials of biomass origin by activation with potassium hydroxide and a comprehensive computer analysis of their porous structure and adsorption properties based on benzene (C6H6) adsorption isotherms were carried out. In particular, the influence of the mass ratio of the activator’s dry mass to the char mass on the formation of the microporous structure of the obtained activated carbons was analysed. The summary of the analyses carried out based on benzene adsorption isotherms begged the conclusion that activated carbon with a maximum adsorption volume in the first adsorbed layer and homogeneous surface can be obtained from ebony wood at a mass ratio of the activator to the char of R = 3. The obtained results confirmed the superiority of the new numerical-clustering-based adsorption analysis (LBET) method over simple methods of porous structure analysis, such as the Brunauer–Emmett–Teller (BET) and Dubinin–Raduskevich (DR) methods. The LBET method is particularly useful in the evaluation of the influence of the methods and conditions of production of activated carbons on the formation of their porous structure. This method, together with an appropriate economic analysis, can help in the precise selection of methods and conditions for the process of obtaining activated carbons at specific manufacturing costs, and thus makes it possible to obtain materials that can successfully compete with those of other technologies used in industrial practice and everyday life.

Neutron Reflection Study of Phenol Adsorbed at the Surface of Its Aqueous Solutions:  An Unusual Adsorbed Layer

1998 ◽  
Vol 102 (1) ◽  
pp. 185-192 ◽  
Author(s):  
Z. X. Li ◽  
R. K. Thomas ◽  
A. R. Rennie ◽  
J. Penfold
Keyword(s):  
Aqueous Solutions ◽  
Adsorbed Layer ◽  
Neutron Reflection

Flow of Hydrophobically Modified Water-Soluble-Polymer Solutions in Porous Media: New Experimental Insights in the Diluted Regime

SPE Journal ◽  
2010 ◽  
Vol 16 (01) ◽  
pp. 43-54 ◽  
Author(s):  
Guillaume Dupuis ◽  
David Rousseau ◽  
René Tabary ◽  
Bruno Grassl
Keyword(s):  
Oil Recovery ◽  
Polymer Concentration ◽  
Adsorbed Layer ◽  
Water Soluble ◽  
Water Soluble Polymer ◽  
Improved Oil Recovery ◽  
Water Soluble Polymers ◽  
Resistance Factors ◽  
Soluble Polymers ◽  
Hydrophobically Modified

Summary The specific molecular structure of hydrophobically modified water-soluble polymers (HMWSPs), also called hydrophobically associative polymers, gives them interesting thickening and surface-adsorption abilities compared with classical water-soluble polymers (WSPs), which could be useful in polymer-flooding and well-treatment operations. However, their strong adsorption obviously can impair their injectivity, and, conversely, the shear sensitivity of their gels can be detrimental to well treatments. Determining for which improved-oil-recovery (IOR) application HMWSPs are best suited, therefore, remains difficult. The aim of this work is to bring new insight regarding the interaction mechanisms between HMWSPs and rock matrix and the consequences concerning their propagation in reservoirs. A consistent set of HMWSPs with sulfonated polyacrylamide backbones and alkyl hydrophobic side chains together with an equivalent WSP was synthesized and fully characterized. HMWSP and WSP solutions were then injected in model granular packs. As expected, with HMWSPs, high resistance factors (or mobility reductions, Rm) were observed. Yet, within the limit of the injected volumes, the effluent showed the same viscosity and polymer concentration as the injected solutions. A first significant outcome concerns the specificities of the Rm curves during HMWSP injections. Rm increases took place in two steps. The first corresponded to the propagation of the viscous front, as observed with WSP, whereas the second was markedly delayed, occurring several pore volumes (PV) after the breakthrough. This result is not compatible with the classical picture of multilayer adsorption of HMWSPs but suggests that injectivity is controlled solely by the adsorption of minor polymeric species. This hypothesis was confirmed by reinjecting the collected effluents into fresh cores; no second-step Rm increases were observed. Brine injections in HMWSP-treated cores revealed high residual resistance factors (or irreversible permeability reductions, Rk), which can be attributed to the presence of thick polymer-adsorbed layers on the pore surface. Nevertheless, Rk values strongly decreased when increasing the brine-flow rate. This second significant outcome shows that the adsorbed-layer thickness is shear-controlled. These new results should lead to proposing new adapted filtration and injection procedures for HMWSPs, aimed, in particular, at improving their injectivity.

Mobility Gradient of Poly(ethylene terephthalate) Chains near a Substrate Scaled by the Thickness of the Adsorbed Layer

2017 ◽  
Vol 50 (17) ◽  
pp. 6804-6812 ◽  
Author(s):  
Jianquan Xu ◽  
Zhenshan Liu ◽  
Yang Lan ◽  
Biao Zuo ◽  
Xinping Wang ◽  
...  
Keyword(s):  
Ethylene Terephthalate ◽  
Adsorbed Layer ◽  
Poly Ethylene Terephthalate ◽  
Poly Ethylene

Manipulating Solid-Surface Properties with Polymeric Agents

1991 ◽  
Vol 249 ◽  
Author(s):  
H. Watanabe ◽  
S.S. Patel ◽  
J.F. Argillier ◽  
E.E. Parsonage ◽  
J. Mays ◽  
...  
Keyword(s):  
Surface Density ◽  
Stable State ◽  
Adsorbed Layer ◽  
Water Soluble ◽  
Interaction Forces ◽  
Interaction Range ◽  
Interparticle Potential ◽  
Copolymer Structure ◽  
The Relationship ◽  
Characteristic Measure

ABSTRACTColloidal processing offers a way to minimize undesired heterogeneities in the fabrication of advanced ceramics. Stable dispersions can be created by manipulation of interparticle potential. Adsorption of diblock copolymer amphiphiles provides a way to obtain long range repulsive interactions between particles, at comparatively low polymer coverage, thereby enabling suspension stabilization. In this study we investigate the relationship between copolymer structure and adsorbed layer characteristics, and specifically, the nature and range of interactions. We find that the surface density and interaction range are governed by a characteristic measure of the copolymer asymmetry. In the case of copolymers where one of the blocks is ionic, and therefore water soluble, we find a hysteresis in the interaction forces, indicating a meta-stable state of the polymer layer.

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