Equilibrium partition

The elution order for neutral species in MEKC depends on the extent to which they partition into the micelles. Hydrophilic neutrals are insoluble in the micelle s hydrophobic inner environment and elute as a single band as they would in CZE. Neutral solutes that are extremely hydrophobic are completely soluble in the micelle, eluting with the micelles as a single band. Those neutral species that exist in a partition equilibrium between the buffer solution and the micelles elute between the completely hydrophilic and completely hydrophobic neutrals. Those neutral species favoring the buffer solution elute before those favoring the micelles. Micellar electrokinetic chromatography has been used to separate a wide variety of samples, including mixtures of pharmaceutical compounds, vitamins, and explosives. [Pg.606]

Partition coefficient Quantitative expression of the partition equilibrium of... [Pg.238]

The relations (pA)a = (fijdp 5 (Fb) = (Pb)p would only by the merest chance form the solution of (2), hence there will not in general be a partition equilibrium between the ions when one is established between the neutral.molecules, but one solvent, say a, will contain more A ions than corresponds with ionic partition equilibrium. These will pass through the surface of contact into /3, and similarly B ions from /3 to a. The separation of the two kinds of ions will however set up an electrostatic field across the boundary, and the two kinds of ions collect there in two sheets very close together—in fact, we have an electrical... [Pg.470]

If there were a simple partition equilibrium, without an electrical potential difference ... [Pg.472]

A recent method, still in development, for determining total 4-nitrophenol in the urine of persons exposed to methyl parathion is based on solid phase microextraction (SPME) and GC/MS previously, the method has been used in the analysis of food and environmental samples (Guidotti et al. 1999). The method uses a solid phase microextraction fiber, is inserted into the urine sample that has been hydrolyzed with HCl at 50° C prior to mixing with distilled water and NaCl and then stirred (1,000 rpm). The fiber is left in the liquid for 30 minutes until a partitioning equilibrium is achieved, and then placed into the GC injector port to desorb. The method shows promise for use in determining exposures at low doses, as it is very sensitive. There is a need for additional development of this method, as the measurement of acetylcholinesterase, the enzyme inhibited by exposure to organophosphates such as methyl parathion, is not an effective indicator of low-dose exposures. [Pg.177]

Other modes of LC operation include liquid-liquid partition chromatography (LLC) and bonded phase chromatography. In the former, a stationary liquid phase which is immiscible with the mobile phase is coated on a porous support, with separation based on partition equilibrium differences of components between the two liquid phases. This mode offers an alternative to ion exchange in the fractionation of polar, water soluble substances. While quite useful, the danger exists in LLC that the stationary phase can be stripped from the column, if proper precautions are not taken. Hence, it is typical to pre-equil-ibrate carefully the mobile and stationary phases and to use a forecolimn, heavily loaded with stationary phase 9). [Pg.227]

The basic principle of every measurement of the Volta potential and generally of the investigations of voltaic cells too, in contrast to galvanic cells, may thus be presented for systems containing metal/solution (Fig. 2) and liquid/liquid interfaces (Fig. 3), respectively. This interface is created at the contact of aqueous and organic solutions (w and s, respectively) of electrolyte MX in the partition equilibrium. Of course, electrolyte MX, shown in Fig. 2 and other figures of this chapter, may be different in organic (s) and aqueous (w) phases. [Pg.17]

According to Eq. (32.10), the distribution potential corresponding to the equilibrium partition of the electrolyte RX is independent of the electrolyte concentration. On the other hand, when more than two ions are involved in the partition equilibrium, there always exists a thermodynamic relationship between the potential difference and the concentrations of ions present. More specifically, let us consider an ITIES with a different electrolyte in each phase. [Pg.612]

Another proposed procedure of finding the ionic data is the application of a special salt bridge, which provides practically constant or negligible liquid junction potentials. The water-nitrobenzene system, containing tetraethylammonium picrate (TEAPi) in the partition equilibrium state, has been proposed as a convenient liquid junction bridge for the liquid voltaic and galvanic cells. [Pg.30]

Using the equation, very strong concentration effects in small systems have been calculated. For instance, if the macroaqueous phase contains 1 M NaCl and 1 /rM NaTPB, the concentration of this electrolyte in the micro-organic phase at partition equilibrium is 1390/rM [14] This approach is valid if the phases in small systems are thick enough (> 1 /rm), in comparison to the Debye screening length, to fulfill the electroneutrality conditions. [Pg.36]

Potential step voltammetry (chronoamperometry) or normal pulse voltammetry (NPV) and potential sweep or cyclic voltammetry (CV) were employed for investigating drugs at the NB/W or DCE/W interface. A thin O-layer cell [15,16,23] was used to realize the partition equilibrium of neutral species (that is, B) at the O/W interface initially at t = 0 within a reasonably short time. All measurements were carried out at 25°C. Experimental details should be consulted in the references cited. [Pg.687]

Having successfully described the variation in DulDj with crystal composition, pressure and temperature, Landwehr et al. (2001) went on to parameterize U-m from their own and published studies in terms of a simple partitioning equilibrium ... [Pg.86]

In order to avoid experiments which are very long, the sampling time was fixed at 60 min. In these conditions, the partition equilibrium for diterpenes extraction is not achieved and SPME does not have maximum sensitivity. However, peak intensities are sufficiently high to detect the presence of diterpenes in a sample. Moreover, a proportional relationship exists between the amount of analyte adsorbed by the SPME fibre and its initial concentration in the sample matrix before reaching partition equilibrium [5, 59]. SPME quantifications are then feasible if necessary, by rigorously reproducing the experimental conditions. [Pg.273]

J. Ai, Headspace solid phase microextraction. Dynamics and quantitative analysis before reaching a partition equilibrium, Anal. Chem., 69, 3260 (1997). [Pg.302]

One aspect to be addressed in order to obtain a realistic vision of the toxicity of these kinds of compounds is their environmental behaviour. Surfactants tend to be adsorbed on particulate matter and thus subsequently to sediment. Consequently, the highest surfactant concentrations are found in sediments, although their distribution is dependent on the partitioning equilibrium between the substrate and interstitial water. This results in two possible routes for uptake (bioaccumulation) and effect. The relative importance of each of these routes depends on the special habits of each benthic organism. [Pg.889]

If a solution of this type is now brought into contact with an organic phase, a partition equilibrium is set up in which, for practical purposes, only the pure aromatic hydrocarbon dissolves in the organic phase. If the organic phase is denoted by a prime, one then finds the partition coefficient to be ... [Pg.233]

Case 4 The interfacial partition between the two phases of unchanged species is fast. The rate is controlled by the diffusion to and away from the interface of the partitioning species. In the absence of an interfacial resistance, the partition equilibrium of A between the aqueous and organic phase, occurring at the interface, can be always considered as an instantaneous process. Here, A is any species, neutral or charged, organic or inorganic. This instantaneous partition process (interfacial equilibrium) is characterized by a value of the partition coefficient equal to that measured when the two phases are at equilibrium. [Pg.241]

If the hetaeron is a detergent or another amphiphile, we also may assume that at sufficiently high concentrations micelles are formed by agglomeration of Hi hetaeron molecules and the solute can be distributed between the mobile phase proper and the micelles in the eluent. The corresponding partition equilibrium can be expressed by... [Pg.121]

MA Schwarz, K Raith, G Dongowski, R Neubert. Effect on the partition equilibrium of various drugs by the formation of mixed bile salt/phosphatidylcho-line/fatty acid micelles. A characterization by micellar affinity capillary electrophoresis. Part IV. J Chromatogr A 809 219-229, 1998. [Pg.139]

An electrolyte, e.g. HCl is shaken up with the two immiscible solvents, water and oil, until the partition equilibrium is arrived at. [Pg.244]

The eoneentration in the water eolumn ean be derived from the eorresponding concentration in the sediment, assuming thermo-dynamie partitioning equilibrium. This ean only be done for the loeations were the fraction organic carbon was measured. For the harmonisation of exposure data to water eoneentrations the formulas 1 and 2 taken from the European Commission Techni-eal Guidanee Doeument on Risk Assessment (EC, 2003) were applied. [Pg.83]

We have determined the ion-pair formation-partition equilibrium constant with picrate anion for a number of primary, secondary, tertiary and quaternary ammonium ions 23>. In aqueous media of pH 5-6, the ammonium ions and picrate are considered to exist almost completely as unpaired counter ions. When the aqueous solution is mixed with an immiscible organic solvent, the ions are partitioned into the organic phase as the ion pair. We expected that the steric effect of N-substituents in the ion-pair formation-partition equilibrium could be analyzed by a procedure similar to Eq. 24, and derived Eq. 27 for the set of quaternary ions 23). [Pg.132]

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