共查询到20条相似文献,搜索用时 3 毫秒
1.
G. M. Pavlov G. F. Kolbina I. I. Gavrilova E. F. Panarin 《Polymer Science Series A》2010,52(2):115-118
For samples of various molecular masses, the flow birefringence of poly(styrene-4-sulfonate sodium) macromolecules in aqueous
solutions at various ionic strengths is studied in relation to the concentration of NaCl. It is shown that the sign of birefringence
changes from negative to positive with an increase in the ionic strength of a solution. Application of the macroform theory
to the Maxwell effect makes it possible to estimate the intrinsic optical anisotropy of the repeating unit of poly(styrene-4-sulfonate
sodium) (a||- a⊥) = −17 × 10-25 cm3), which nearly coincides with similar values known for atactic polystyrene and poly(κ-methylstyrene). 相似文献
2.
Ling-Xin Wang Xiao-Man Yu Qing Xia Feng-Bao Zhang Guo-Liang Zhang 《The Journal of chemical thermodynamics》2012,44(1):128-132
The solubility data of sodium 4-nitrotoluene-2-sulfonate (NTSNa) in aqueous organic solutions (propanol + water) and (ethylene glycol + water) were measured at temperatures ranging from (290 to 351) K using a dynamic method. The mole fraction of water in solvent mixtures ranged from 0 to 0.8. The solubility values are correlated with the electrolyte non-random two-liquid (E-NRTL) model. From the results obtained, the E-NRTL model provides a satisfactory mathematical representation of the experimental results for the (NTSNa + propanol + water) system and an unsatisfactory result for the (NTSNa + ethylene glycol + water) system. Thus, the modified Apelblat model is applied to describe the (NTSNa + ethylene glycol + water) system also. The calculated (solid + liquid) equilibrium temperatures with the modified Apelblat model are in good agreement with the experimental results. The root-mean-square deviations of solubility temperature varied from (0.08 to 0.94) K for two models. The effect of different aqueous organic solutions on the reaction of oxidation 4-nitrotoluene-2-sulfonic acid (NTS) to 4,4′-dinitrostilbene-2,2′-disulfonic acid (DNS) was discussed. 相似文献
3.
N. M. Panich B. G. Ershov A. F. Seliverstov A. G. Basiev 《Russian Journal of Applied Chemistry》2007,80(11):1812-1815
The effect exerted by the concentration of salts (NaCl, Na2SO4, and NaNO3) on the ozone solubility in aqueous solution at 20, 30, and 40°C was studied. The solubility coefficients of ozone were calculated. The Henry constants and the Sechenov coefficients were determined. 相似文献
4.
The solubility of toluene has been measured in distilled water, and in various inorganic salt solutions. Values of the Setschenow constant, K(S), which quantify toluene solubility versus salt concentration, have been determined for each salt. Values of K(S) are compared to the activity of water for the salt solutions. Data from this study, consistent with earlier data, suggests that the effects of salts upon toluene solubility are non-additive. This contrasts the additive behavior of inorganic salts upon the solubility of nonpolar organic compounds, such as benzene and naphthalene, reported in the literature. Specific interaction between slightly polar toluene and ions in solution is suggested as a possible explanation for the non-additive effect of salts on the solubility of toluene. 相似文献
5.
G. M. Pavlov A. S. Gubarev I. I. Gavrilova E. F. Panarin 《Polymer Science Series A》2011,53(11):1003-1011
Translational friction and viscosity of dilute solutions of sodium poly(styrene-4-sulfonate) with molecular masses of M = (5 × 104)−(85 × 104) are studied at different concentrations of low-molecular-mass salts. Molecular masses of the polymer are determined from
the sedimentation-diffusion data. The study of the correlation between molecular masses and hydrodynamic characteristics resulted
in ascertainment of the Kuhn-Mark-Houwink-Sakurada relationships for salt-free aqueous solutions of the polymer and solutions
of the polymer in 0.2 M NaCl, 4.17 M NaCl, and 1.0 M KCl. It is shown that, as the ionic strengths of solutions are varied
from minimum (H2O) to maximum (4.17 M), macromolecules of the strong polyelectrolyte sodium poly(styrene-4-sulfonate) change their conformations
from rigid rods to coils and, then, approach a globular conformation. In terms of the Gray-Bloomfield-Hearst and Yamakawa-Fujii
theories and within the framework of the weakly bent cylinder model, the statistical Kuhn segment length and the hydrodynamic
diameter of sodium poly(styrene sulfonate) chains are estimated in 0.2 and 4.17 M NaCl, 1.0 M KCl, and salt-free aqueous solutions.
The electrostatic component of the equilibrium rigidity is taken into account within the framework of the Odijk-Fixman-Skolnick
and Dobrynin theories. 相似文献
6.
A platinum-lined, flowing autoclave facility is used to investigate the solubility behavior of copper(II) oxide (CuO) in aqueous sodium phosphate solutions at temperatures between 19 and 262°C. Copper solubilities are observed to increase continuously with temperature and phosphate concentration. The measured solubility behavior is examined via a Cu(II) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reactions are obtained from a leastsquares analysis of the data. Altogether, thermochemical properties are established for five anionic complexes: Cu(OH)
3
–
, Cu(OH)
4
2–
, Cu(OH)
2
(HPO
4
)
2–
, Cu(OH)
3
(H
2
PO
4
)
2–
, and Cu(OH)
2
(PO
4
)
3–
. Precise thermochemical parameters are also derived for the Cu(OH)+ hydroxocomplex based on CuO solubility behavior previously observed (Ref. 3) for pure water at elevated temperatures. The relative ease of Cu(II) ion hydrolysis is such that Cu(OH)
3
–
species become the preferred hydroxocomplex for pH9.4.Prepared for presentation at the Fourth International Symposium on solubility Phenomena, Rensselaer Polytechnic Institute, August 1990. 相似文献
7.
The kinetic features of potassium persulfate-initiated homogeneous radical copolymerization of sodium 2-acrylamido-2-methylpropanesulfonate (M1) with sodium acrylate (M2) in concentrated aqueous solutions and NaCl aqueous solutions at pH 9 and T = 60°C have been studied. The initial rate of copolymerization increases with the concentration of each monomer, the total concentration of comonomers (M1 + M2), the concentration of initiator, and the concentration of NaCl and shows an extreme change with an increase in the content of M2 in the initial monomer mixture. The molecular mass of the copolymer shows an extreme dependence on the content of M2 in the initial monomer mixture; it drops with an increase in the concentration of NaCl and remains unchanged with conversion. For copolymerization in water and 2 M NaCl, r 2 > r 1. The number of M2 units in the copolymer does not change with conversion and increases on addition of NaCl owing to a gain in r 2. 相似文献
8.
A. V. Levanov I. V. Kuskov E. E. Antipenko V. V. Lunin 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2008,82(12):2045-2050
The solubility of ozone and the kinetics of its decomposition and interaction with chloride ions in a 1 M aqueous solution of NaCl at 20°C and pH 8.4–10.8 were studied. The ratio between the concentration of O3 in solution and the gas phase was found to be 0.16 at pH 8.4–9.8. The concentration of dissolved ozone decreased sharply as pH increased to 10.8 because of a substantial increase in the rate of its decomposition. It was observed for the first time that the interaction of O3 with Cl? in alkaline media resulted in the formation of ClO 3 ? chlorate ions. The dependence of the rate of formation of ClO 3 ? on pH was determined; its maximum value was found to be 9.6 × 10?6 mol l?1 min?1 at pH 10.0 and the concentration of ozone at the entrance of the reactor 30.0 g/m3. A spectrophotometric method for the determination of chlorate ions (concentrations 1 × 10?5?3 × 10?4 M) in aqueous solutions was suggested. 相似文献
9.
The influence of sodium dodecyl sulfate on the dissociation of protonated 8-hydroxyquinoline in aqueous solutions is investigated by potentiometric titration at 293 K. The constants of direct binding of 8-hydroxyquinoline with the monomers and micelles of sodium dodecyl sulfate are determined by the computer simulation of the most probable processes. The role of electrostatic and hydrophobic interactions in the studied system is discussed.__________Translated from Kolloidnyi Zhurnal, Vol. 67, No. 2, 2005, pp. 231–234.Original Russian Text Copyright © 2005 by Ramenskaya, Vladimirova. 相似文献
10.
King AD 《Journal of colloid and interface science》2004,273(1):313-319
Measurements have been made to determine the solubilities of ethane, C2H6, propane, C3H8, and carbon dioxide, CO2, in aqueous solutions of sodium cumene sulfonate (NaCS) at 25 degrees C. The solubilities measured for each gas satisfy Henry's law at all concentrations of NaCS. The solubilities of C2H6 and C3H8 exhibit quite similar behavior with respect to added NaCS. The solubilities of these two gases are very low in pure water and are found to be nearly independent of NaCS concentration over a concentration range of 0-0.4 mol NaCS/kg H2O. At intermediate concentrations of NaCS, the solubilities of C2H6 and C3H8 exhibit a gradual increase with added NaCS concentrations ranging from 0.4 to 2.0 mol NaCS/kg H2O. At NaCS concentrations greater than 2.0 mol NaCS/kg H2O, the solubilities of these two gases increase with added NaCS in an approximately linear manner, with the solubility of C3H8 increasing more rapidly than that for C2H6 (by a factor of approximately 2.5). CO2 is much more soluble in pure water than the hydrocarbon gases and exhibits markedly different behavior with respect to added NaCS. The solubility of CO2 decreases with added NaCS over a concentration range of 0-0.9 mol NaCS/kg H2O, passes through a minimum at a concentration of approximately 1.0 mol NaCS/kg H2O, and then increases with added NaCS at higher NaCS concentrations in a manner similar to that observed with C2H6 and C3H8. The trends in solubility observed for these three gases dissolved in aqueous solutions of NaCS resemble those found previously with aqueous solutions of ordinary surfactants. The solubility data measured for these three gases can be interpreted surprisingly well in terms of the mass-action model for micellization, in which salting-out effects due to monomer salt ions suppress gas solubility at low NaCS concentrations and gas solubilization by small micelles of NaCS acts to enhance gas solubility at the higher NaCS concentrations. 相似文献
11.
The effect of the concentration of the initial monomer mixture, the comonomer ratio, and temperature on the kinetic parameters of the process and the characteristics of the resulting copolymers in the homogeneous copolymerization of sodium 2-acrylamido-2-methylpropanesulfonate with sodium acrylate in aqueous solutions at 50–80°C in the presence of potassium persulfate is studied. The initial rate of copolymerization and the molecular mass of copolymers increase with the total initial concentration of the monomer mixture and the content of sodium 2-acrylamido-2-methylpropanesulfonate. As temperature increases, the initial rate of copolymerization increases and the molecular mass of the copolymer diminishes. When copolymerization is performed in 10, 30, and 40% aqueous solutions of the monomers, the resulting copolymers are enriched in sodium acrylate units. The content of sodium 2-acrylamido-2-methylpropane-sulfonate units in the copolymer slightly increases with an increase in the total initial concentration of the monomer mixture. 相似文献
12.
13.
14.
S. E. Ziemniak 《Journal of solution chemistry》1992,21(8):745-760
The solubility behavior of metal oxides in sub- and super-critical aqueous solutions is quantified using thermodynamic concepts. Three physicochemical phenomena are discussed: (1) metal oxide solid phase stability; (2) metal oxide dissolution reaction equilibria; and (3) metal ion hydroxocomplex formation. Thermochemical properties of metal oxides/ions representative of the most common constituents of construction metal alloys, i.e., elements having atomic numbers between 22 (Ti) and 30 (Zn), are summarized on the basis of metal oxide solubility studies conducted at General Electric and elsewhere.Presented at the Second International Symposium on Chemistry in High Temperature Water, Provo, UT, August 1991. 相似文献
15.
A platinum-lined, flowing autoclave facility is used to investigate the solubility/phase behavior of zinc(II) oxide in aqueous sodium phosphate solutions at temperatures between 17 and 287°C. ZnO solubilities are observed to increase continuously with temperature and phosphate concentration. At higher phosphate concentrations, a solid phase transformation to NaZnPO4 is observed. NaZnPO4 solubilities are retrograde with temperature. The measured solubility behavior is examined via a Zn(II) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reaction equilibria are obtained from a least-squares analysis of the data. The existence of two new zinc(II) ion complexes, Zn(OH)2(HPO4)2– and Zn(OH)3(H2PO4)2–, is reported for the first time. A summary of thermochemical properties for species in the systems ZnO–H2O and ZnO–Na2O–P2O5–H2O is also provided. 相似文献
16.
Accurate modeling of the solubility behavior of CO2 in the aqueous alkanolamine solutions is important to design and optimization of equipment and process. In this work, the thermodynamics of CO2 in aqueous solution of N-methyldiethanolamine (MDEA) and piperazine (PZ) is studied by the electrolyte non-random two liquids (NRTL) model. The chemical equilibrium constants are calculated from the free Gibbs energy of formation, and the Henry’s constants of CO2 in MDEA and PZ are regressed to revise the value in the pure water. New experimental data from literatures are added to the regression process. Therefore, this model should provide a comprehensive thermodynamic representation for the quaternary system with broader ranges and more accurate predictions than previous work. Model results are compared to the experimental vapor-liquid equilibrium (VLE), speciation and heat of absorption data, which show that the model can predict the experimental data with reasonable accuracy. 相似文献
17.
Salt solutions have been the object of study of many scientists through history, but one of the most important findings came along when the Hofmeister series were discovered. Their importance arises from the fact that they influence the relative solubility of proteins, and solubility is directly related to one of today's holy grails: protein folding. In this work we characterize one of the more-destabilizing salts in the series, sodium perchlorate, by studying it as an aqueous solution at various concentrations ranging from 0.08 to 1.60 mol/L. Molecular dynamics simulations at room temperature permitted a detailed study of the organization of solvent and cosolvent, in terms of its radial distribution functions, along with the study of the structure of hydrogen bonds in the ions' solvation shells. We found that the distribution functions have some variations in their shape as concentration changes, but the position of their peaks is mostly unaffected. Regarding water, the most salient fact is the noticeable (although small) change in the second hydration shell and even beyond, especially for g(O(w)***O(w)), showing that the locality of salt effects should not be restricted to considerations of only the first solvation shell. The perturbation of the second shell also appears in the study of the HB network, where the difference between the number of HBs around a water molecule and around the Na(+) cation gets much smaller as one goes from the first to the second solvation shell, yet the difference is not negligible. Nevertheless, the effect of the ions past their first hydration shell is not enough to make a noticeable change in the global HB network. The Kirkwood-Buff theory of liquids was applied to our system, in order to calculate the activity derivative of the cosolvent. This coefficient, along with a previously calculated preferential binding, allowed us to establish that if a folded AP peptide is immersed in the studied solution, becoming the solute, then increasing the salt concentration will make the helix more stable. 相似文献
18.
《Fluid Phase Equilibria》2006,244(2):117-127
The electrolyte–NRTL model used in a previous work (B. Messnaoui, T. Bounahmidi, Fluid Phase Equilibr. 237(1–2) (2005) 77–85), was extended for modeling of α-hemihydrate and gypsum solubilities in the complex system Ca2+–H+–SO42−–HSO4−–H2PO4−–H3PO4–H2O, at wide range of temperature and P2O5 concentration. The chemical equilibrium constant was evaluated as function of temperature according to the Gibbs–Helmholtz equation. The temperature dependence was taken into account in the expression of the standard state heat capacity of ionic, molecular and cristalline salts species. The standard-state heat capacity of Ca2+at 298.15 K is calculated to be 27.30 J mol−1 K−1. It is also shown that the experimental data agree with the predicted values of gypsum and anhydrite solubilities in water, at high temperature, by using only the values of parameters , which were calculated, at 298.15 K from data of gypsum solubilities in phosphoric acid solutions. 相似文献
19.
Solubility measurements over the pH range 2.6–7.6 for tetracycline, chlortetracycline, dimethylchlortetracycline and oxytetracycline are used to determine thermodynamic values for the solubility constant and the first and second acidity constants of these compounds. 相似文献
20.
A cost‐effective and environmentally friendly method to dissolve microcrystalline cellulose (MCC) has been utilized. A detailed investigation of the effects of cellulose amount and solvent (aqueous NaOH) concentration on MCC solubility has been presented. In the experiments, NaOH solutions with concentrations ranging from 3.7 to 18.6 wt% have been employed to dissolve MCC with various weights. The results show that an optimal NaOH concentration range can always be found to give the best solubility of MCC having a certain weight. The solubility monotonically decreases with either the decreasing or increasing of NaOH concentration away from the optimal concentration range. In addition, the optimal concentration range of NaOH for dissolving cellulose has been shown to shrink as the amount of MCC increases. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献