scholarly journals Adsorption of lauryl sulphonic acid in the surface of its aqueous solution, and the Gibbs theorem

The absolute amount of adsorption per square centimetre of exposed surface of a solution may be measured with certainty and with moderate accuracy. In the microtome method (McBain and Humphreys 1932; McBain and Swain 1936; McBain, Ford and Mills 1940) the quiescent surface is cut from a solution in complete equilibrium with its vapour, collected, and analysed. In the interferometer method (Ford and McBain 1936; McBain, Mills and Ford 1940) a similar surface in equilibrium is compressed into the bulk of the liquid in the path of an interferometer beam which measures excess coming from the known surface destroyed. Both methods applied to solutions of lauryl sulphonic acid, C 12 H 25 SO 3 H, agree in showing strong positive adsorption over the whole range of concentrations. On the other hand, the curve of surface tension with concentration is of Type III, showing very great lowering in extreme dilution, leading immediately to a minimum, followed by a definite rise to a shallow maximum, with a slight decrease of this already low value with further concentration. The Gibbs theorem demands an initial positive adsorption of the acid, followed by no adsorption at all where the surface tension is most lowered, followed by strong negative adsorption, then zero adsorption, still in dilute solution with very low surface tension, followed by slight positive adsorption.

2012 ◽  
Vol 16 (02) ◽  
pp. 210-217 ◽  
Author(s):  
Jin Matsumoto ◽  
Shin-ichio Tanimura ◽  
Tsutomu Shiragami ◽  
Masahide Yasuda

Water-soluble phosphorus tetraphenylporphyrins (1) were prepared by the introduction of axial polyoxaalkyloxo ligands (–O–(CH2CH2O)m–(CH2)n–H) . Bioaffinity of 1 for Saccharomyces cerevisiae was evaluated on the basis of the concentration (B A ) of 1 absorbed into the cells after they were immersed into an aqueous solution of 1 (10 μM). The behavior of 1 in the concentration range from 1 μM to 0.1 mM were estimated by measuring surface tension and absorption spectra and the behavior at a concentration of 1 mM were estimated by NMR spectroscopy. The 1 (m = 2, n = 4; m = 1, 2 and 3, n = 6) with a high B A of 123–171 mM were solved as monomers at 10 μM and could pass through the cell wall to accumulate inside the cell. Once inside the cell, where they reached a concentration of more than 10 μM, they formed aggregates that were unable to escape to the outside of the cell. On the other hand, it was found that 1 (m = 2 and 3, n = 1; m = 2, n = 2), whose B A values were <24 mM, did not form aggregates in the range from 1 μM to 1 mM; this indicated that they easily passed through the cell wall in both directions. In the case of 1 (m = 2 and 3, n = 12), whose B A values were low, passage through the cell wall was not possible because aggregates formed even at <1 μM.


2017 ◽  
Vol 18 ◽  
pp. 01028
Author(s):  
Tomasz Ratajczak

Flotation data on copper-bearing shale in aqueous solutions of inorganic electrolytes (NaCl, Na2SO4, KPF6, NH4Cl) and organic reagents (ethylamine, propylamine) as frothers were presented and discussed. The relationships between shale flotation, surface tension of aqueous solution and foam height during bubbling with air in the flotation system were presented. It has been found that flotation of shale in the presence of inorganic salts the yield was directly proportional to the surface tension of the aqueous solution of salt and inversely proportional to the height of the foam. On the other hand, for organic reagents solutions (short chain amines), a reverse effect has been observed in relation to the inorganic compounds studied, that is the yield of copper-bearing shale flotation and the foam height were inversely proportional to the surface tension of the amine solution.


Author(s):  
K. T. Tokuyasu

During the past investigations of immunoferritin localization of intracellular antigens in ultrathin frozen sections, we found that the degree of negative staining required to delineate u1trastructural details was often too dense for the recognition of ferritin particles. The quality of positive staining of ultrathin frozen sections, on the other hand, has generally been far inferior to that attainable in conventional plastic embedded sections, particularly in the definition of membranes. As we discussed before, a main cause of this difficulty seemed to be the vulnerability of frozen sections to the damaging effects of air-water surface tension at the time of drying of the sections.Indeed, we found that the quality of positive staining is greatly improved when positively stained frozen sections are protected against the effects of surface tension by embedding them in thin layers of mechanically stable materials at the time of drying (unpublished).


Entropy ◽  
2021 ◽  
Vol 23 (2) ◽  
pp. 242
Author(s):  
Joanna Halun ◽  
Pawel Karbowniczek ◽  
Piotr Kuterba ◽  
Zoriana Danel

The calculations of the dimensionless layer monomer density profiles for a dilute solution of phantom ideal ring polymer chains and star polymers with f=4 arms in a Θ-solvent confined in a slit geometry of two parallel walls with repulsive surfaces and for the mixed case of one repulsive and the other inert surface were performed. Furthermore, taking into account the Derjaguin approximation, the dimensionless layer monomer density profiles for phantom ideal ring polymer chains and star polymers immersed in a solution of big colloidal particles with different adsorbing or repelling properties with respect to polymers were calculated. The density-force relation for the above-mentioned cases was analyzed, and the universal amplitude ratio B was obtained. Taking into account the small sphere expansion allowed obtaining the monomer density profiles for a dilute solution of phantom ideal ring polymers immersed in a solution of small spherical particles, or nano-particles of finite size, which are much smaller than the polymer size and the other characteristic mesoscopic length of the system. We performed molecular dynamics simulations of a dilute solution of linear, ring, and star-shaped polymers with N=300, 300 (360), and 1201 (4 × 300 + 1-star polymer with four arms) beads accordingly. The obtained analytical and numerical results for phantom ring and star polymers are compared with the results for linear polymer chains in confined geometries.


2000 ◽  
Vol 406 ◽  
pp. 337-346 ◽  
Author(s):  
L. ENGEVIK

The instabilities of a free surface shear flow are considered, with special emphasis on the shear flow with the velocity profile U* = U*0sech2 (by*). This velocity profile, which is found to model very well the shear flow in the wake of a hydrofoil, has been focused on in previous studies, for instance by Dimas & Triantyfallou who made a purely numerical investigation of this problem, and by Longuet-Higgins who simplified the problem by approximating the velocity profile with a piecewise-linear profile to make it amenable to an analytical treatment. However, none has so far recognized that this problem in fact has a very simple solution which can be found analytically; that is, the stability boundaries, i.e. the boundaries between the stable and the unstable regions in the wavenumber (k)–Froude number (F)-plane, are given by simple algebraic equations in k and F. This applies also when surface tension is included. With no surface tension present there exist two distinct regimes of unstable waves for all values of the Froude number F > 0. If 0 < F [Lt ] 1, then one of the regimes is given by 0 < k < (1 − F2/6), the other by F−2 < k < 9F−2, which is a very extended region on the k-axis. When F [Gt ] 1 there is one small unstable region close to k = 0, i.e. 0 < k < 9/(4F2), the other unstable region being (3/2)1/2F−1 < k < 2 + 27/(8F2). When surface tension is included there may be one, two or even three distinct regimes of unstable modes depending on the value of the Froude number. For small F there is only one instability region, for intermediate values of F there are two regimes of unstable modes, and when F is large enough there are three distinct instability regions.


2005 ◽  
Vol 47 (2) ◽  
pp. 185-202 ◽  
Author(s):  
T. E. Stokes ◽  
G. C. Hocking ◽  
L. K. Forbes

AbstractThe unsteady axisymmetric withdrawal from a fluid with a free surface through a point sink is considered. Results both with and without surface tension are included and placed in context with previous work. The results indicate that there are two critical values of withdrawal rate at which the surface is drawn directly into the outlet, one after flow initiation and the other after the flow has been established. It is shown that the larger of these values corresponds to the point at which steady solutions no longer exist.


2014 ◽  
Vol 70 (11) ◽  
pp. 1054-1056 ◽  
Author(s):  
Qiang Li ◽  
Hui-Ting Wang

A new cadmium dicyanamide complex, poly[tetramethylphosphonium [μ-chlorido-di-μ-dicyanamido-κ4N1:N5-cadmium(II)]], [(CH3)4P][Cd(NCNCN)2Cl], was synthesized by the reaction of tetramethylphosphonium chloride, cadmium nitrate tetrahydrate and sodium dicyanamide in aqueous solution. In the crystal structure, each CdIIatom is octahedrally coordinated by four terminal N atoms from four anionic dicyanamide (dca) ligands and by two chloride ligands. The dicyanamide ligands play two different roles in the building up of the structure; one role results in the formation of [Cd(dca)Cl]2building blocks, while the other links the building blocks into a three-dimensional structure. The anionic framework exhibits a solvent-accessible void of 673.8 Å3, amounting to 47.44% of the total unit-cell volume. The cavities in the network are occupied by pairs of tetramethylphosphonium cations.


2009 ◽  
Vol 6 (s1) ◽  
pp. S153-S158 ◽  
Author(s):  
Tariq S. Najim ◽  
Suhad A. Yassin

Modified pomegranate peel (MPGP) and formaldehyde modified pomegranate peel (FMPGP) were prepared and used as adsorbent for removal of Cr(VI) ions from aqueous solution using batch process. The temperature variation study of adsorption on both adsorbents revealed that the adsorption process is endothermic, from the positive values of ∆H˚. These values lie in the range of physisorption. The negative values of ∆G˚ show the adsorption is favorable and spontaneous. On the other hand, these negative values increases with increase in temperature on both adsorbents, which indicate that the adsorption is preferable at higher temperatures. ∆S˚ values showed that the process is accompanied by increase in disorder and randomness at the solid solution interface due to the reorientation of water molecules and Cr(VI) ions around the adsorbent surface. The endothermic nature of the adsorption was also confirmed from the positive values of activation energy, Ea, the low values of Ea confirm the physisorption mechanism of adsorption. The sticking probability, S*, of Cr(VI) ion on surface of both adsorbents showed that the adsorption is preferable due to low values of S*(0< S*< 1 ), but S*values are lower for FMPGP indicating that the adsorption on FMPGP is more preferable .


1860 ◽  
Vol 150 ◽  
pp. 379-408

When my paper on the Conductivity of various Substances was presented to the Society, it was intimated to me on the part of the Council of the Society, that it might be advisable to determine absolute instead of relative conductivities, the latter being alone attempted in my previous experiments. It has been partly in consequence of this intimation, as well as from the desire to make my investigations the more complete, that I have given my attention to the construction of a calorimeter which might serve for this purpose. The present communication contains a description of this instrument, with the results which it has enabled me to obtain respecting the absolute quantities of heat which emanate from the surfaces of certain substances under given conditions. 1. When a body is placed in atmospheric air (or any gas), the quantity of heat which is lost from its surface in a given time, when its temperature is higher than that of the surrounding medium, will be greater than if it were placed in a vacuum, other conditions remaining unaltered. In the latter case the heat escapes by simple radiation; in the other case a portion of the heat also escapes in consequence of the contact of the air with the surface of the heated body. Dulong and Petit ascertained by a careful series of experiments, the laws according to which the mercury contained in the bulb of a thermometer cools, or those which govern the quantity of heat which escapes from the surface of the containing bulb, when placed in a vacuum, in air, or in several kinds of gases. These experiments were made with the glass bulb naked, and also when it was silvered, so that the laws of radiation which they established were strictly in reference only to surfaces of glass and those of silver. Certain laws were identical in both these cases, and hence it was concluded, though by a limited induction, that the same laws were applicable to all other surfaces. They did not, however, give the absolute quantity of heat which, under given circumstances, and in a given time, emanates from the surfaces of the glass or silver with which they experimented. The instrument which I have constructed gives very easily this absolute amount of heat, as I believe, with very approximate accuracy.


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