Some solvent effects on the solvent extraction of 8-quinolinol

The distribution constants of 8-quinolinol between water and a series of substituted aliphatic hydrocarbons, at 25 degrees , are reported. The results are discussed in terms of dielectric constant and solubility parameter of the solvents. For 8-quinolinol, and possibly for its chelates, bromochloromethane, dibromomethane and chloroform seem to be about the best solvents, in that order. Among the solvents studied, chloroform shows significantly higher values than expected; the deviation may be explained as a specific interaction of the hydrogen- bonding type.     

Effect of solvent type on formation of PVC‐solvent complex

The effect of solvent type on the structural features of PVC gels prepared from the solutions of dibutyl phthalate(DBP) and butyl benzoate(BB) were investigated. The influence of solvent type, i.e., diester solvent or monoester solvent, on the mechanical responses was characterized by dynamic viscoelastic measurements as a function of temperature, aging time, and PVC concentration. In the case of PVC/DBP aged gels, the transition phenomenon appeared close to 50°C, whereas no such transitions were observed for PVC/BB aged gels. This transition is considered to be associated with polymer‐solvent complex which can be accounted for electrostatic interaction between C=O bond of solvent and H‐C‐Cl part of PVC. While BB solvent molecules can not form polymer‐solvent complex due to no capacity to act as a bridge between PVC molecular chains. FT‐IR spectroscopy and DSC investigation on either PVC/DBP gels or PVC/BB gels was reported and discussed together with the mechanical behavior. Electron micrographs of the dried gel prepared from the critical point drying technique reveal that the gel morphology consists of well developed three dimensional fibrous network structure independent of solvent type.     

Studies of solvent effects

The effect of water on the conformational preferences of acetylcholine has been studied within the discrete, the continuum and the combined discrete-continuum models described in parts I and II of this series. All the models lead to the conclusion that the trans-gauche form which is, following refined quantum-mechanical computations, the intrinsically preferred one and the one observed in the crystal of acetylcholine and of a number of analogues should remain also the preferred conformation in water. This result agrees with NMR studies. The results of the empirical discrete model used here compare favorably to those obtained by an ab initio super-molecule treatment. The continuum model utilized here represents a net improvement above such models utilized in other works.     

Implicit nonpolar solvent models

We have systematically analyzed a new nonpolar solvent model that separates nonpolar solvation free energy into repulsive and attractive components. Our analysis shows that either molecular surfaces or volumes can be used to correlate with repulsive free energies of tested molecules in explicit solvent with correlation coefficients higher than 0.99. In addition, the attractive free energies in explicit solvent can also be reproduced with the new model with a correlation coefficient higher than 0.999. Given each component optimized, the new nonpolar solvent model is found to reproduce monomer nonpolar solvation free energies in explicit solvent very well. However, the overall accuracy of the nonpolar solvation free energies is lower than that of each component. In the more challenging dimer test cases, the agreement of the new model with explicit solvent is less impressive. Nevertheless, it is found that the new model works reasonably well for reproducing the relative nonpolar free energy landscapes near the global minimum of the dimer complexes.     

Radical electrophilicities in solvent

A series of Ti-doped SnO₂(110) surfaces with different oxygen vacancies have been investigated by means of first principles DFT calculations combined with a slab model. Three kinds of defective SnO₂(110) surfaces are considered, including the formations of bridging oxygen (O _b ) vacancy, in-plane oxygen (O _i ) vacancy, and the coexistence of O _b and O _i vacancies. Our results indicate that Ti dopant prefers the fivefold-coordinated Sn site on the top layer for the surface with O _b or O _i vacancy, while the replacement of sublayer Sn atom becomes the most energetically favorable structure if the O _b and O _i vacancies are presented simultaneously. Based on analyzing the band structure of the most stable configuration, the presence of Ti leads to the variation of the band gap state, which is different for three defective SnO₂(110) surfaces. For the surface with O _b or O _i vacancy, the component of the defect state is modified, and the reaction activity of the corresponding surface is enhanced. Hence, the sensing performance of SnO₂ may be improved after introducing Ti dopant. However, for the third kind of reduced surface with the coexistence of O _b and O _i vacancies, the sublayer doping has little influence on the defect state, and only in this case, the Ti doping state partly appears in the band gap of SnO₂(110) surface.     

The solvent dimethyl sulfoxide

The dipolar aprotic solvent dimethyl sulfoxide is liquid over a wide range of temperatures, is a strong electron donor, and has a high polarity. It is therefore an excellent and selective solvent for many organic and even polymeric compounds, and can enter into H-bonding and dipole-dipole association. The structure of dimethyl sulfoxide, with a “hard” oxygen atom and a “soft” sulfur atom, leads to good solvation of cations and poor solvation of anions. Mixtures of alkoxides with dimethyl sulfoxide are therefore among the most strongly basic systems in organic chemistry, and are excellently suited for the deprotonation of weakly acidic OH, NH, and CH bonds, for eliminations, and for the initiation of polymerizations.     

Evaluation of free-volume theories for solvent self-diffusion in polymer–solvent systems

An evaluation of free-volume theories for solvent self-diffusion is carried out using recent comprehensive data sets for penetrant self-diffusion in polymer solutions. Different theories are compared, and free-volume theories in the prediction of penetrant self-diffusion coefficients in glassy polymer systems is also evaluated. © 1993 John Wiley & Sons, Inc.     

A model for predicting solvent self-diffusion coefficients in nonglassy polymer/solvent solutions

Cohen-Turnbull diffusion theory is used to develop a model for predicting solvent self-diffusion coefficients D₁ in nonglassy polymer/solvent solutions. Polymer molecules are envisioned as hindering solvent mobility by reducing the average free volume per unit mass in the system and through the lower mobility of polymer segments relative to solvent molecules. The concentration dependence of D₁ predicted by the model is in reasonable agreement with data for the solvents heptane, hexadecane, benzene, cyclohexane, and decalin in polyisobutylene (PIB), and for toluene in polystyrene, poly(methyl mothacrylate), and PIB. Although none of the data is for high concentrations of polymer (volume fractions ?≥0.9) it is anticipated the model will be less representative in this regime where the assumptions in its development are unsure. The model also demonstrates the correct temperature and concentration dependence of the apparent activation energy for diffusion. The only experimental data needed to use the model are the viscosity and critical volume of the pure solvent, and the specific volume of both the solvent and mixture. No binary transport data are required.     

Comparison of solvent mixtures for pressurized solvent extraction of soil fatty acid biomarkers

The extraction and transesterification of soil lipids into fatty acid methyl esters (FAMEs) is a useful technique for studying soil microbial communities. The objective of this study was to find the best solvent mixture to extract soil lipids with a pressurized solvent extractor system. Four solvent mixtures were selected for testing: chloroform:methanol:phosphate buffer (1:2:0.8, v/v/v), chloroform:methanol (1:2, v/v), hexane:2-propanol (3:2, v/v) and acetone. Soils were from agricultural fields and had a wide range of clay, organic matter and microbial biomass contents. Total lipid fatty acid methyl esters (TL-FAMEs) were the extractable soil lipids identified and quantified with gas chromatography and flame ionization detection. Concentrations of TL-FAMEs ranged from 57.3 to 542.2 n mole g⁻¹ soil (dry weight basis). The highest concentrations of TL-FAMEs were extracted with chloroform:methanol:buffer or chloroform:methanol mixtures than with the hexane:2-propanol or acetone solvents. The concentrations of TL-FAMEs in chemical groups, including saturated, branched, mono- and poly-unsaturated and hydroxy fatty acids were assessed, and biological groups (soil bacteria, mycorrhizal fungi, saprophytic fungi and higher plants) was distinguished. The extraction efficiency for the chemical and biological groups followed the general trend of: chloroform:methanol:buffer ≥ chloroform:methanol > hexane:2-propanol = acetone. Discriminant analysis revealed differences in TL-FAME profiles based on the solvent mixture and the soil type. Although solvent mixtures containing chloroform and methanol were the most efficient for extracting lipids from the agricultural soils in this study, soil properties and the lipid groups to be studied should be considered when selecting a solvent mixture. According to our knowledge, this is the first report of soil lipid extraction with hexane:2-propanol or acetone in a pressurized solvent extraction system.     

有机质子溶剂和有机-水溶液中质子浓度的精确测定

用水标准溶液标定的玻璃电极可用来测定有机质子溶剂和有机-水溶液中质子的水标准活度pHm质子的浓度可用-og[H2S^ ]=pHm-(-logγ-D)来精确测定。(-logγ-D)是一个常数，可以通过对有机质子溶剂和有机-水溶液中强酸-强碱滴定曲线的数学模拟后求得。因此避免了玻璃电极在有机溶剂中标定的困难。     

Solvent dependent reactivity: solvent activation vs. solvent coordination in alkylphosphane iron complexes

The pyridine-derived tetrapodal tetraphosphane C5H3N[CMe(CH2PMe2)2]2 is susceptible to selective protonolysis of a phosphorus-carbon bond in the presence of iron(II) salts. Water produces dimethylphosphinic acid, Me2POH, and protonates the anionic remainder of the tetraphosphane. The resulting iron(II) complexes and (tetrafluoroborate and perchlorate salts, respectively) contain the residual chelate ligand in which a methyl group, derived from the ligand skeleton, is in agostic interaction with the metal centre, and in which Me2POH, unavailable in the free state owing to rapid tautomerisation, is metal-coordinated and thus stabilised. Full NMR details are presented, including 31P simulations. The reactivity towards alcohols is similar (compounds), and has been studied using deuterium labels (NMR). P-C bond cleavage may be suppressed only if all protic agents are rigorously excluded, as in the reaction of with Fe(SO3CF3)2.2CH3CN in acetonitrile solution, which produces the complex [Fe(NCMe)](SO3CF3)2. In it, the ligand acts as an NP4 coordination cap but is severely distorted from square-pyramidal geometry. The reaction of with anhydrous ferrous bromide, FeBr2, in methanol again produces a dimethylphosphinic acid ester ligand, but the complex now contains ferric iron coordinated by a carbanionic residual chelate ligand, implicating H+ as the oxidising agent under these conditions. Full spectroscopic and X-ray structural details are presented for all compounds.     

T2 relaxation measurement with solvent suppression and implications to solvent suppression in general

A number of suppression pulse sequences including Excitation Sculpting and WATERGATE were incorporated into the standard Carr‐Purcell‐Meiboom‐Gill (CPMG) program for T₂ measurement and experimentally evaluated. The chosen suppression schemes were of varying complexity encompassing pulse program elements, such as presaturation, gradients, and selective pulses, which are typically utilized for solvent suppression. The quality of the spectral data and the accuracy of T₂ measurements of the investigated suppression schemes were evaluated using three aqueous samples with increasing proton content in the water solvent, i.e. by volume 100% D₂O, 80/20% D₂O/H₂O, and 20/80% D₂O/H₂O. For signals removed from the water signal, the T₂ values were generally very consistent between all pulse sequences tested. T₂ measurements can be unreliable for signals too close to the water signal such that they are significantly suppressed as well. Their intensity may actually grow initially through cross relaxation that transfers magnetization back to the solute signal. In turn, this relaxation phenomenon can be exploited to improve the spectral quality of conventional solvent suppression schemes. In favorable cases, even signals that are completely masked by the water signal can be recovered by adding a carefully chosen number of spin echoes with optimized evolution time to conventional water suppression pulse programs, such as Excitation Sculpting or WATERGATE. Copyright © 2009 John Wiley & Sons, Ltd.     

Experimental analysis and thermodynamic modelling of Nitroxynil solubility in pure solvent and binary solvent

Nitroxynil(NIT) is a commonly used anti-liver fluke drug for cattle and sheep, Its solubility is closely related to its preparation. In this work, the molar solubility of NIT in nine pure solvents (methanol, ethanol, 1,2-propanediolethyl, isopropanol, ethyl acetate, acetonitrile, n-butanol, phemethylol) and two kinds of binary mixtures with different ratio(ethanol + phemethylol; ethanol + acetonitrile) was determined by shake flask method over the temperature from 278.15 ～ 323.15 K at atmosphere pressure. Results show that the solubility of NIT in all tested solvents was increased with raised temperature. In mono-solvents, the mole fraction solubility of NIT was highest in phemethylol and the solubility order is: phemethylol > acetonitrile > ethyl acetate > methanol > n-butanol > ethanol > 1,2-propanediolethyl > isopropanol > water. In binary solvents, the mole fraction solubility increased with increasing ratio of phemethylol/acetonitrile. In mono-solvents, the modified Apelblat equation, λh equation, Van't Hoff model were applied to correlate the solubility data. In binary solvents, the modified Apelblat equation, λh equation, GSM model and Jouyban-Acree model were to correlate the solubility data. Solubility order of NIT in nine pure solvent and two binary solvent systems were analysed by using the Hansen solubility parameter (HSP). Activity coefficient was to access the solute–solvent molecular interactions. In addition, the dissolution of NIT is an endothermic and entropy-friendly process, since thermodynamic parameters such as enthalpy, entropy, and apparent standard Gibbs free energy are all greater than zero. The results will supply some essential data on recrystallization process, purification and formulation development of NIT in pharmaceutical applications.     

Water-organic solvent systems in countercurrent chromatography: Liquid stationary phase retention and solvent polarity

Countercurrent chromatography (CCC) is a separation technique in which the stationary phase is a liquid. The liquid stationary phase retention is a critical problem in CCC. The retention of 18 organic solvents in a hydrodynamic CCC apparatus was measured with an aqueous mobile phase, the centrifuge spin rate and the mobile phase flow rate being constant, 800 rpm and 2 ml/min, respectively. Conversely, water retention was measured when the 18 solvents were the mobile phases. A direct relationship between the liquid stationary phase retention and the phase density difference was found. The liquid phase density difference is the most important parameter for stationary phase retention in a hydrodynamic CCC apparatus with coiled tubes. The chromatographic retention of formanilide was measured in biphasic systems and expressed as the formanilide partition coefficient. It is shown that the partition coefficient correlates with the Reichardt polarity index of the organic solvent when the liquid stationary phase retention volume does not.     

Anion-exchange in mixed solvent systems

A quantitative separation scheme for 15 radionuclides is presented. The scheme is based on group separation by means of anion-exchange resins using mixed solvent systems and subsequent separation of the groups into individual components by means of change of both eluting agent and resin type. The optimum working conditions for separation are established. Separation procedures are of good reproducibility and practically quantitative.     

Catalytic effects in solvent extraction

Catalytic phenomena in solvent extraction of metals with hydrophobic chelating extractants are reviewed. Interface modification by adsorption of additives, phase transfer catalysis, formation of micelles, reversed micelles and microemuslions are discussed and examples are given.     

Supercritical water as a solvent

Water is not restricted to moderate temperatures and low pressures, but can exist up to very high temperatures, far above its critical point at 647 K. In this supercritical regime, water can be gradually compressed from gas-like to liquid-like densities. The resulting dense supercritical states have extraordinary properties which can be tuned by temperature and pressure, and form the basis for innovative technologies. This Review covers the current knowledge of the major properties of supercritical water and its solutions with nonpolar, polar, and ionic compounds, and of the underlying molecular processes.