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Model formulations aqueous

Solution chemistry. Note that C, in the surface complexation model formulation is the free ion concentration, while in the Langmuir isotherm it is the total analytical concentration. In reality, the formation of aqueous complexes will change the surface adsorption (affecting the term C,). The speciation of i may also change with time. [Pg.204]

A typical pharmaceutical formulation will serve as model, frozen aqueous solutions that are contained in loosely stoppered glass vials. They stand directly on the freeze-drier shelves. Such a model appears deceptively simple but is in fact subject to considerable complexities that bedevil the modelling of optimum processing conditions and the estimation of a realistic drying cycle time. As emphasised in earlier chapters, for the case where the product does not display eutectic behaviour, it is imperative to freeze the solution to below Tg, in order to ensure maximal freeze-concentration and minimise deleterious chemical reactions that have been shown to occur at high rates in part frozen, supersaturated mixtures.By the same token, the temperature during the removal of ice by sublimation must on no account be allowed to rise above T at... [Pg.105]

The ultimate objective of this handbook is to enable the practicing engineer to effectively formulate and solve mathematical models for aqueous electrolyte systems. In this chapter, several electrolyte systems of practical interest are examined and the formulation and solution of the attendant simulation models are reviewed. [Pg.577]

Figure 4.50. Cumulative dissolution results. Two experimental tablet formulations were tested against each other in a dissolution test in which tablets are immersed in a stirred aqueous medium (number of tablets, constructional details and operation of apparatus, and amount of medium are givens). Eighty or more percent of the drug in either formulation is set free within 10 minutes. The slow terminal release displayed by formulation B could point towards an unwanted drug/excipient interaction. The vertical bars indicate ymean - with Sy 3%. A simple linear/exponential model was used to approximate the data for the strength 2 formulation. Strengths I and 3 are not depicted but look very similar. Figure 4.50. Cumulative dissolution results. Two experimental tablet formulations were tested against each other in a dissolution test in which tablets are immersed in a stirred aqueous medium (number of tablets, constructional details and operation of apparatus, and amount of medium are givens). Eighty or more percent of the drug in either formulation is set free within 10 minutes. The slow terminal release displayed by formulation B could point towards an unwanted drug/excipient interaction. The vertical bars indicate ymean - with Sy 3%. A simple linear/exponential model was used to approximate the data for the strength 2 formulation. Strengths I and 3 are not depicted but look very similar.
The aggregation and surface properties of Cardax, 3.19, in various aqueous formulations were comprehensively evaluated in 2005 (Foss et al. 2005c), as well as the potential plasma protein binding in mammalian applications with molecular modeling (Zsila et al. 2003). Cardax, 3.19, proved... [Pg.51]

An aqueous dope of forms gel with protonic acid, alkali, oxidizing and reducing agents as formulated below. The crosslinking of S-S type would be suggested since the formation of -SH or -S was confirmed for the model compound under the similar condition. [Pg.55]

Most research on aroma recovery by organophilic pervaporation has been conducted using aqueous aroma model solutions [25-28], although in recent years significant interest has been devoted to the recovery of aroma compounds from natural complex streams, such as fruit juices [29-31], food industry effluents [32] and other natural matrixes [33]. The increasing demand for natural aroma compounds for food use, and their market value, opens a world of possibilities for a technique that allows for a benign recovery of these compounds without addition of any chemicals or temperature increase. However, in most situations, dedicated requests by industrialists are formulated in cooperation with marketing departments, which translate into the need for a correct public perception. [Pg.436]

Generalized local Darcy s model of Teorell s oscillations (PDEs) [12]. In this section we formulate and study a local analogue of Teorell s model discussed previously. The main difference between the model to be discussed and the original one is the replacement of the ad hoc resistance relaxation equation (6.1.5) or (6.2.5) by a set of one-dimensional Nernst-Planck equations for locally electro-neutral convective electro-diffusion of ions across the filter (membrane). This filter is viewed as a homogenized aqueous porous medium, lacking any fixed charge and characterized... [Pg.220]

Clinical use Parecoxib (Cheer and Goa, 2001 Gotta, 2001 Sorbera et al., 2001b) is a third generation COX-2 inhibitor. Parecoxib is a prodrug of valdecoxib with aqueous solubility sufficient for the use of the substance in parenteral formulations. Valdecoxib shows about 30-fold selectivity for COX-2 in whole blood assays (see Valdecoxib Talley et al., 2000a Riendeau et al., 2001). Parecoxib shows efficacy in a variety of animal models of inflammation (Talley et al., 2000b). [Pg.96]

It is assumed that treated water cannot be reinjected. The aqueous concentration at thirteen observation wells must be less than or equal to the water quality goal (0.5 mg/L) by the end of a 5-year remediation period. The locations of these potential extraction wells and observation wells are indicated in Figure 1. Thus, to complete the formulation of this problem, the following three constraints must be added to the management model described in Equations 4 to 11 ... [Pg.8]

Extension of the equilibrium model to column or field conditions requires coupling the ion-exchange equations with the transport equations for the 5 aqueous species (Eq. 1). To accomplish this coupling, we have adopted the split-operator approach (e.g., Miller and Rabideau, 1993), which provides considerable flexibility in adjusting the sorption submodel. In addition to the above conceptual model, we are pursuing more complex formulations that couple cation exchange with pore diffusion, surface diffusion, or combined pore/surface diffusion (e.g., Robinson et al., 1994 DePaoli and Perona, 1996 Ma et al., 1996). However, the currently available data are inadequate to parameterize such models, and the need for a kinetic formulation for the low-flow conditions expected for sorbing barriers has not been established. These issues will be addressed in a future publication. [Pg.130]

The species concentrations are formulated in activities using the Pitzer model (207) for the aqueous phase and the Hildebrand-Scott solubility parameter (208) for the organic phase. [Pg.387]

The model was formulated on the basis of a set of material balances, for each of the species involved in the aqueous phase ... [Pg.284]

Not unexpectedly, the widespread and continuing interest in water has prompted many molecular models for water (Perram and Levine, 1974 Ives and Lemon, 1968 Frank, 1973). We will not review all the attempts at formulating a structure for water. This brief account will reflect the opinions of the author and recognize that in chemists terms we are interested in providing a basis for a discussion of the properties of aqueous solutions. The overiding difficulty is that an account of water structure also reflects the general problems involved in describing the liquid state (Powles, 1974). [Pg.236]


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