scholarly journals Surface Active Properties and Micellar Features of Copper Soaps Derived from Various Edible Oils

2018 ◽  
Vol 5 (1) ◽  
pp. 119-133 ◽  
Author(s):  
Arun Kumar Sharma ◽  
Meenakshi Saxena ◽  
Rashmi Sharma

Introduction:The molar volume, viscosity, specific viscosity, and fluidity of copper surfactant derived from various edible oils in methanol -benzene solvent have been determined at a constant temperature 303 K.Methods / Results:The results were used to calculate (CMC), soap complex-solvent interactions and the effect of chain length of the surfactant molecule on various parameters.The conclusions with regard to soap-soap and soap- methanol -benzene interaction have been discussed in terms of well-known Moulik’s and Jones- Dole equations. The effect of surfactant concentration on viscosity of the solution in solvent mixture has been discussed.Conclusion:The observations suggested that the structure breaking effect by the solute on the solvent molecules is more prominent above CMC as compared to below CMC after the formation of the micelles. The vital information plays an important role in various industrial process as well as biological applications.

2019 ◽  
Vol 9 (2) ◽  
pp. 123-137
Author(s):  
Arun Kumar Sharma ◽  
Meenakshi Saxena ◽  
Rashmi Sharma

Background: Of-late researches in colloid chemistry are becoming increasingly important in various branches of chemistry, industry, medicine and allied fields. Copper surfactants derived from various edible oils provide an interesting area of investigation pertaining to its fundamental information regarding their colloid-chemical behaviour. Copper (II) soaps and their urea complexes in polar and non-polar solvents have gained considerable popularity due to their immense use and widespread applications such as wood preservation, foaming, wetting, biocidal, pesticidal activities, fungicidal, detergency, emulsification, paints, lubrication etc. Objective: Present work has been initiated with a view to obtain a profile due to the nature and structure of copper soap and their urea complexes with long chain fatty acids in polar and non-polar solvent, which have great significance in explaining their characteristics under different conditions. The objective of the present work is study of micellar characterizations of copper soap and their urea complexes in polar (methanol) and non-polar (benzene) solvents of varying composition and subsequent determinations of CMC using physical properties such as, viscosity. This will provide fundamental information regarding their colloid chemical behavior. Methods: The density, molar volume, viscosity, specific viscosity, and fluidity of Cu (II) soap- urea complexes derived from various edible oils in a benzene-methanol solvent system have been determined at a constant temperature of 303.15 K. Results: Results: The results were used to determine the critical micelle concentration (CMC), soap complex-solvent interactions and the effect of chain length of the surfactant molecules on various parameters. The values of the CMC in the higher volume percent of methanol are higher than those of the lower volume percent of methanol. The values of CMC for these complexes are following the order: CSoU>CSeU> CGU > CMU : This shows that there is a decrease in the CMC values with an increase of the average molecular weight of the complex. The conclusions with regard to solute-solute and solutesolvent interactions have been discussed in terms of the well-known Moulik’s and Jones- Dole equations. The effect of surfactant concentration on the viscosity of the solution in the solvent mixtures has been discussed. The observations suggested that the solvent structure breaking effect by the solute on the solvent molecules is more prominent above the CMC as compared to below the CMC. Conclusion: The vital information about the micellar behavior of synthesized molecules as a solute and their interactions with different solvents will plays an important role in various industrial and biological applications.


1992 ◽  
Vol 57 (11) ◽  
pp. 2227-2234 ◽  
Author(s):  
Ján Benko ◽  
Oľga Vollárová

The enthalpies of solution ∆Hs0 were determined for NaSCN, KSCN, NaBrO3, KBrO3, NaClO3, KClO3, NaIO4, KMnO4, KNO2 and NaNO2 in water-methanol mixtures. The transfer functions ∆Ht0 of the salts and anions were calculated based on the extrathermodynamic TPTB assumption. The ∆Ht0 values of the anion obtained from the sodium and potassium salts were compared. The differences observed, particularly at higher concentrations of the cosolvent, are discussed with respect to the interactions between the solvent molecules and the solute-solvent interactions.


2020 ◽  
Vol 22 (3) ◽  
pp. 1525-1533 ◽  
Author(s):  
Luisa Weirich ◽  
Juliana Magalhães de Oliveira ◽  
Christian Merten

A VCD spectroscopic analysis of selected model systems for solute–solvent interactions of chiral diols with hydrogen bonding solvents DMSO and ACN.


2016 ◽  
Vol 22 (3) ◽  
pp. 598-602
Author(s):  
Daniela Babuşca ◽  
Cezarina Ana Moroşanu ◽  
Dana Ortansa Dorohoi

Abstract The wavenumbers in the maximum of intramolecular charge transfer (ICT) visibile band of two pyridazinium ylids binary solutions were analized using Kamlet and Taft empirical parameters and the Hildebrand’s solubility parameter. The Hildebrand’s solubility parameter values, δH2, measures the energy needed to separate the solvent molecules. A linear solvation energy relationship (LSER) allows separating the contributions of different types of interactions to the total spectral shift. The supply of universal and specific interactions as well as the supply of solvent-solvent interactions to the total spectral shifts was calculated.


2019 ◽  
Vol 9 (3) ◽  
pp. 232-246
Author(s):  
Neha Mathur ◽  
Biplab Manna ◽  
Arun Kumar Sharma

Background: Phenothiazines and Triphenodithiazines are included in the class of nitrogen and sulphur donating ligands. They have a wide spectrum of biological activities and form important class of heterocyclic compounds. Both drugs are being used as, antitumors, anti-inflammatory, antiviral, anaesthetics, anticancer agents, antimalarials, antimicrobials, anti-cholinergics, growth inhibitors, and many other pharmacological agents. Objective: Present work has been initiated with a view to obtain a profile regarding structural insight of complexes of Cobalt (II), Ni (II) and Zinc (II) soaps derived from substituted phenothiazines 15 and triphenodithiazines using latest technique. It also gives an account of micelle formation in the mixed non aqueous solvents. Methods: The viscosity, specific viscosity, and fluidity of complexes of Co, Ni, and Zn Oleate with substituted phenothiazine and triphenodithiazine in methanol + benzene solvents was determined at a constant temperature of 303.15 K to study the micellar features and critical micelle concentration (CMC). In the present work benzene+ methanol have selected as co solvents due to these interact with complex molecules and thus affected aggregation of complex molecules. Results: The results were used to determine the CMC, soap complex-solvent interactions and the effect of chain length of the surfactant molecule on various parameters. The conclusions concerning solute-solute and solute-solvent interaction were discussed regarding the well-known Moulik’s and Jones-Dole equations. Conclusion: From above results it may be concluded that the micelle formation take place earlier in the case of triphenodithiazine complexes due to larger molecular structure, so a smaller number of molecules are needed to form micelle. Micellization also confirms the existence of complex aggregation in the non-aqueous mixed solvents. To conclude, it can be unveiled on the basis of the result acquired that above study of complexes conforms the presence of complex aggregation in the non - aqueous mixed solvents.


2008 ◽  
Vol 63 (7-8) ◽  
pp. 493-504 ◽  
Author(s):  
Durvas S. Bhuvaneshwari ◽  
Kuppanagounder P. Elango

Substitution reactions of some para-substituted anilines with 2-bromo-5-nitropyridine are carried out conductometrically in binary acetonitrile/dimethylformamide mixtures. The second-order rate constants correlate well with Hammett’s substituent constants yielding a negative value of ρ. The multiparameter correlation with Kamlet-Taft’s solvatochromic parameters is excellent (100R2 ~ 98%), and the computed percentage contributions of these parameters (Pα = 58%, Pβ = 4%, Pπ∗ = 38%) suggest that both specific and non-specific solute-solvent-solvent interactions influence the reactivity. The solvation model proposed is well supported by the solvatochromism exhibited by the anilines in the solvent mixture under investigation. The molar extinction coefficient (εmax) of aniline varies appreciably up to ~ 25% with a change in the mole fraction of the mixture. The multivariate correlation analysis of εmax (with α, β , π∗) suggests that the solvation around the NH2 moiety of aniline through the solvent’s hydrogen-bond donor (HBD) property is found to be dominant in the solvation process and consequently in altering the rate. The dominance of the solvent’s HBD property in solvation is further confirmed by the cyclic voltammetric oxidation of aniline in the solvent mixture.


Author(s):  
MA Yousuf ◽  
KM Salim Reza ◽  
Md Moniruzzaman ◽  
MA Aziz ◽  
MA Salam

The densities, ρ and viscosities, η of NH4Cl, NiCl2 and FeCl3 in dimethylsulfoxide were studied as a function of concentration. The partial molal volume, (φ0v) of these electrolytes were evaluated. The viscosity and viscosity-coefficients (A and B) were also determined by Jones-Dole equation. B-coefficient for NiCl2 and FeCl3 are positive that show structure making behavior in all the solutions while those of NH4Cl are negative indicating structure breaking properties. The coefficient A represents the solute-solute interactions coupled with size and shape effect of the solute and to some extent solute-solvent interactions. The behaviors of three solutes in binary systems were discussed in terms of the charge, size and hydrogen bonding effect. Keywords: Density, Apparent and partial molal volume, viscosity coefficient. DOI: 10.3329/diujst.v4i2.4360 Daffodil International University Journal of Science and Technology Vol.4(2) 2009 pp.15-18


1972 ◽  
Vol 50 (6) ◽  
pp. 834-838 ◽  
Author(s):  
Avijit Purkayastha ◽  
John Walkley

Data are presented for the saturation solubility and partial molal volume of iodine in a mixed benzene–cyclohexane solvent and for the saturation solubility of stannic iodide in the same solvent mixture. A successful interpretation of these data in terms of solubility parameter theory is possible if we define an effective volume fraction term. This term reflects the immediate solvent environment of the solute molecule with the preferential solvation of the solute by one of the solvent molecules. Data for iodine in a mixed carbon tetrachloride–benzene solvent mixture and for iodine in a carbon tetrachloride–perfluoroheptane mixture are also interpreted in terms of the proposed theory.


2016 ◽  
Vol 12 (2) ◽  
Author(s):  
Debasmita Dash ◽  
C. Mallika ◽  
U. Kamachi Mudali

Abstract Viscosities of binary mixtures of polyethylene glycol-1000 (PEG-1000) and water were measured precisely in the temperature range 293.15–343.15 K at atmospheric pressure using a high precision viscometer. Viscosity data were used to calculate the activation energy of viscous flow. The activation energy was observed to increase with increase in the concentration of aqueous solutions of PEG which indicated that more energy is required to move the molecule inside the structure with increase in concentration. The measured data provided better understanding to explain the behaviour of macromolecules with respect to change in concentration and temperature. The results were discussed in the light of polymer-solvent interactions. At lower concentration range, the molecules exhibit weak interaction due to dominant repulsive force and at higher concentration the entanglement of polymer chain increases. In view of greater force of interaction between solute and solvent molecules forming hydrogen bonding, there will be an increase in interaction with temperature and concentration.


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