The effect of high pressure on the ion pair equilibrium constant of alkali metal fluorides: A spectrophotometric study

Bromophenol blue indicator was used in UV-visible spectrophotometric measurements to study ion association constants of alkali metal fluorides. The equilibrium constants for the ion pair formation of the alkali metal fluorides were determined as a function of ionic strength at one atmosphere pressure and 25°C. The effect of pressure on these association constants was measured at a constant total ionic strength of 1.0 mol-kg^–1 over a pressure range of 1 to 2000 atmospheres at 25°C. The pressure dependences of the stoichiometric association constants of the alkali metal fluorides are given by: lnK _LiF ^* =0.77–2.47×10^–4P–2.12×10^–8P²; lnK _NaF ^* =0.53–1.08×10^–4P–1.66×10^–8P²; lnK _KF ^* =0.24–4.41×10^–5P–7.15×10^–8P²; lnK _RbF ^* =–0.17–8.65×10^–5P–4.51×10^–8P²; and lnK _CsF ^* = –0.37–1.14×10^–4P–6.82×10^–8P², where P is the pressure in atmospheres. The stoichiometric molar volume and compressibility changes for ion pair formation of the alkali metal fluorides were evaluated from the pressure dependence of K _MF ^* data. The thermodynamic association constants were also calculated making use of activity coefficient data from the Pitzer equations. The partial molal volume and compressibility changes for ion pair formation of each alkali metal fluoride are reported.     

Fluorine-Stabilized Sulfur–Carbon Multiple Bonds

Alkylidene and alkylidyne sulfur fluorides contain sulfur–carbon multiple bonds. In contrast to the sulfur ylides, alkylidene sulfur fluorides fulfill all the criteria for double bonds, i.e. they have short bond lengths, strong anisotropic distribution of electron density, and rotation about the C? S bond is restricted. Alkylidyne sulfur fluorides have especially short bond distances and, due to a high amplitude bending motion, appear to be more or less linear, depending on the physical state. The advantage of the C? S multiple bond systems in contrast with numerous others, e.g. those of phosphorus and silicon, is that they exist without steric stabilization. Moreover, the limits of the triple-bond principle are outlined: the prognosis for triple bonds between two elements of higher periods is poor, because carbene-like or fully bridged structures win in terms of stability.     

Conductometric study of Bu4NClO4 in propylene carbonate-acetonitrile and propylene carbonate-toluene mixtures at 25°C

Conductometric measurements of tetrabutylammonium perchlorate in propylene carbonate-acetonitrile and propylene carbonate-toluene mixtures at 25°C are reported. Limiting molar conductances, association constants and distance of closest approach of ions are calculated. The experimental data were analyzed by means of the Lee-Wheaton equation. The Gilkerson's solvent-solute interaction energy term was calculated from a plot of association constant logarithmvs. reciprocal dielectric constant.     

Group contributions to the infinite dilution partial molar volumes of alkanes, alcohols, and glycols in polar organic solvents

Densities of binary mixtures of polar organic solvents with alcohols were measured at 25‡C. The solvents studied were N,N-dimethylformamide, dimethylsulfoxide, and formamide while alcohols were butanol, pentanol, hexanol, and 1,4-butanediol. Density measurements of hydrocarbons (from pentane to dodecane and some heptane isomers) + N,N-dimethylformamide were also performed. From these data the apparent molar volumes of alcohols and hydrocarbons as functions of concentration were calculated. The standard partial molar volumes were obtained by extrapolation to infinite dilution and are discussed in terms of group contributions.     

Influence of hydrophobe content on the solution rheology of hydrophobically modified terpolymer of SO2, N,N-diallyl-N-carboethoxymethylammonium chloride

Rheological properties of hydrophobically modified copolymer of SO₂, N,N-diallyl-N-carboethoxymethylammonium chloride and the hydrophobic monomer N,N-diallyl-N-octadecylammonium chloride were studied. The influence of hydrophobe content (HP) and polymer concentration was investigated. Polymers with HP content in the range 1.5-5% were examined and the concentration was varied in the range 2-5 wt%. Both dynamic and steady-shear experiments were performed in ARES rheometer. Copolymers were observed to exhibit typical viscoelastic behavior even with low HP content. Both the dynamic viscosity, η′ and storage modulus, G′, increase with the increase of both the polymer concentration and the HP content of the system. The viscosity of the high HP content polymer showed a strong shear dependency, while G′ was a weak function of frequency and gel-like behavior was observed. The zero-shear viscosity, η₀, showed a strong concentration dependency (η₀ ∼ ?^α; 1.1 < α < 5.9). The concentration dependency of η₀ suggests that intermolecular association is dominant in the high HP content polymer. Control of the HP content and polymer concentration of this class of polymers can lead to a wide range of interesting rheological properties.     

Seawater—A test of multicomponent electrolyte solution theories. I. The apparent equivalent volume,expansibility, and compressibility of artificial seawater

The apparent equivalent volume _V, expansibility _E, and compressibility _K of an artificial seawater solution containing10 ionic components (Na⁺, Mg²⁺, Ca²⁺, K⁺, Sr²⁺, Cl^–, SO ₄ ^2– , HCO ₃ ^– , Br^–, and F^–) and one nonionic component (H₃BO₃) has been determined from0 to40°C (in5° intervals) and from0.1 to0.8 m ionic strength at1 atm. The concentration dependence (I_v=volume ionic strength) of the _V's, _E's, and _K's have been examined by using a Masson-type equation, = ^° +S'I _V ^1/2, and a Redlich-type equation, = ^° +SI _V ^1/2 +BI _V, where ^° is the infinite-dilution value, S is the empirical Masson slope, S is the theoretical Debye-Hückel slope, and B is an empirical deviation constant. By using Young's rule, = E_i(i), the apparent equivalent volumes, expansibilities, and compressibilities for sea salt have been estimated from the ionic and nonionic components making up the mixture. The estimated apparent molal quantities agree very well with the directly measured values providing the concentration terms, S _i and B_i, are weighted according to the methods of Wood and Reilly.Contribution Number 1599 from the University of Miami.     

The effect of pressure on the dissociation constant of hydrofluoric acid and the association constant of the NaF ion pair at 25°C

The effect of pressure on the dissociation constant of hydrofluoric acid was determined by using the indicator technique at 25°C at an ionic strength of 0.1m over a pressure range of 1 to 2000 atm. A value of 3.14 for pK _a ^* at I =0 was obtained by extrapolation to zero ionic strength at 1 atm. The pressure dependence yielded a partial molar volume change of –9.6 cm³-mol^–1 and a compressibility change of — 35×10^–3 cm³-mol^–1 –atm^–1 for the dissociation. The dependence of ionic strength on the association constant K _A ^* of NaF was studied at 25°C and 1 atm. Extrapolation to I=0 yielded a pK _A ^* of –0.78. The pressure dependence of K _A ^* gave a change of volume of 3.26 cm³-mol^–1 and a change in compressibility of 6×10^–3 cm³-mol^–1-atm^–1 for the formation of the ion pair.     

Interactions between Adsorbed Layers of a Low Charge Density Cationic Polyelectrolyte on Mica in the Absence and Presence of Anionic Surfactant

Interactions between two negatively charged mica surfaces across aqueous solutions containing various amounts of a 10% charged cationic polyelectrolyte have been studied. It is found that the mica surface charge is neutralized when the polyelectrolyte is adsorbed from a 10–50 ppm aqueous solution. Consequently no electrostatic double-layer force is observed. Instead an attractive force acts between the surfaces in the distance regime 250–100 Å. We suggest that this attraction is caused by bridging. Additional adsorption takes place when the polyelectrolyte concentration is increased to 100 and 300 ppm, and a long-range repulsion develops. This repulsive force is both of electrostatic and steric origin. The polyelectrolyte layer adsorbed from a 50 ppm solution does not desorb when the polyelectrolyte solution is replaced with an aqueous polyelectrolyte-free solution. Injection of sodium dodecyl sulfate (SDS) into the measuring chamber to a concentration of about 0.01 CMC (8.3 × 10⁻⁵M) does not affect the adsorbed layers or the interaction forces. However, when the SDS concentration is increased to 0.02 CMC (0.166 mM) the adsorbed layer expands dramatically due to adsorption of SDS to the polyelectrolyte chains. The sudden swelling suggests a cooperative adsorption of SDS to the preadsorbed polyelectrolyte layer and that the critical aggregation concentration between the polyelectrolyte and SDS at the surface is about 0.02 CMC. The flocculation behavior of the polyelectrolyte in solution upon addition of SDS was also examined. It was found that 0.16–0.32 mol SDS/mol charged segments on the polyelectrolyte is enough to make the solution slightly turbid.     

Electroconductivity of the calcium oxide-ethylene glycol-water system

The electroconductivity of calcium oxide-ethylene glycol (EG) and calcium oxide-EG-water systems is measured in wide ranges of temperatures and compositions. With increasing temperature, the conductivity of the former system passes through a maximum, which shifts to lower temperatures with increasing electrolyte concentration. Thermodynamic characteristics of the calcium hydroxy glycolate association in EG are estimated using the Lee-Wheaton equation. The conductivity of the latter system decreases with increasing EG content. Its dependence on the limiting high-frequency conductivity of the mixed solvent is analyzed. The activation energy for conduction in both systems decreases with increasing temperature and electrolyte concentration.     

计量置换参数Z值分量的测定(英文)

 以计量置换吸附理论(SDT A)为基础,从理论上推导出计量吸附模型中表征溶质对固定相亲合势大小的参数βa值与流动相中强置换剂浓度的对数呈线性关系。计量置换模型中的参数n和q(n和q分别代表1摩尔溶剂化溶质被吸附时,从吸附剂表面和从溶质分子表面所释放出的溶剂的物质的量)是计量置换参数Z值的分量,是两个非常有用的参数,可以从这个定量关系中直接获得。推导出的方程用苯的衍生物进行了实验验证,获得了较满意的结果。将这种方法计算得到的分量值与SDT A与计量置换保留模型(SDT R)相结合的方法得到的分量值进行了比较。