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Assessment and Selection of Dispersants

These are by far the most quantitative methods for the assessment of dispersing power. Known amounts of solids (in grams) with a surface area A (m g ) are equilibrated at a constant temperature with dispersant solutions of various concentrations, Cj. The bottles containing the various dispersions are rotated for several hours until equilibrium is reached, after which the particles are removed from the dispersant solution by centrifugation and/or filtration through Millipore filters. The dispersant concentration in the supernatant liquid, C2, is analytically determined by a suitable technique that can measure low concentrations. [Pg.391]

In both cases a plateau adsorption value F is reached at a given value of C2. In general, the value of F is reached at a lower C2 for polymeric surfactant adsorption when compared to small molecules. The high-affinity isotherm obtained with polymeric surfactants implies that the first added molecules are virtually [Pg.391]


Although there are many biocide alternatives available on the market, for example enzyme technology or bio-dispersants, there appears to be a continued requirement for the use of biocides in order to reduce the levels of microbiological contamination entering the paper making process. The increased awareness of environmental and safety aspects will continue to play an important role on the selection of biocides for paper making processes. The use of legislation to select biocides must be done in parallel with each plants internal risk assessment. No one biocide active will meet all the criteria set out by different European countries and hence the use of these actives must be carefully assessed on a plant by plant basis. [Pg.22]

St and divinylbenzene (DVB) were polymerized in a dispersion of acryl-amide-methacrylic acid-methylenebisacrylamide terpolymer particles (25). Fine polystyrene particles were formed in/on each seed terpolymer particle. The former was smaller by about one-twentieth than the latter. The distribution of polystyrene particles depended on the cross-link density. Different amounts of St and DVB were charged in the seeded polymerization, and the resulting composite particles were used for protein adsorption measurement to assess the hydrophobicity of the particle surface. The adsorbed amount was almost proportional to the amount of St and DVB charged. In contrast, cells were less stimulated by the 5% St-containing particle than by the 0% St-containing one, that is, the seed particle. This phenomenon is attributed to selective protein adsorption on the 5% St-containing particle (26). [Pg.655]

To identify comparable non-critical areas, N02 and PM levels and the trend of these pollutants were analysed in cities across the EU. Taking the criteria for non-critical areas into account, Berlin was selected as a comparable non-critical area.7 Other cities or areas which fit the criteria for non-critical areas either have a special emission structure (which eases abatement measures), or they are comparably small, or largely comparable to Berlin with respect to their dispersion conditions or modal split of traffic in several cases the available information about air quality assessment and management is not enough. Therefore, Berlin is the only non-critical area which is discussed here in detail. [Pg.8]

Table 1 summarizes the information required for a detailed characterization of a supported metal catalyst for supported bimetallics there are additional questions, e.g., the distribution of atoms in bimetallic clusters and the surface composition of larger alloy crystallites. For the support and the prepared catalyst, the total surface area, pore size distribution, and surface acidity are routinely measured, if required, while other characteristics, e.g., thermal and chemical stability, will have been assessed when selecting the support. The surface structure of alumina, silica, charcoal, and other adsorbents used as catalyst supports has been reviewed. Undoubtedly, the most commonly measured property is the metal dispersion, often expressed in terms of the specific metal area and determined by selective chemisorption or titration but, as discussed (Section 2), there is the recurring problem of deciding the correct adsorption stoicheiometry. [Pg.31]

To date, theoretical studies of the thermodynamic behavior of water clusters have been limited to model potentials [41-45,47,84], although there have been studies that examined the temperature dependence of selected isomers [67,73] and others that have used DFT-based MD simulations to optimize structures and to calculate vibrational spectra [7]. In the absence of either experimental or ab initio data on the thermodynamic properties of small water clusters, it is difficult to assess the reliability of the simulations carried out with various model potentials. Although simulations of the thermodynamic properties of small water clusters are feasible with DFT methods, it has been found that DFT calculations with commonly employed functionals such as Becke3LYP [86,87] incorrectly order various isomers of small water clusters [88]. This appears to be due to the inability of current density functionals to describe long-range dispersion interactions [89,90]. For this reason, it is preferable that finite temperature simulations of water clusters be carried out using an appropriate wavefunction-based electronic stmcture method. [Pg.997]

The polymer serves as a carrier in which API is dispersed in an ASD. Polymer selection is very important as it influences manufacturing, bioavailability, and stability of the ASD. Initial assessment of potentially useful excipients should be based on basic physicochemical properties of the polymers such as glass transition temperature (Tg), hygroscopicity, solid solution capacity and solubilization capacity to name a few. [Pg.123]

Process technology selection for the manufacture of amorphous solid dispersions requires consideration of the particular complexities of the drug and excipients. HME offers the possibility to manufacture drug products in a continuous, cost-effective manner, yet it presents unique challenges that must be tackled. Noting the significant interplay between formulation and process, a risk-based classification system has been developed to aid in the early assessment of dispersion success using melt extrusion. [Pg.204]


See other pages where Assessment and Selection of Dispersants is mentioned: [Pg.391]    [Pg.85]    [Pg.314]    [Pg.315]    [Pg.317]    [Pg.319]    [Pg.391]    [Pg.85]    [Pg.314]    [Pg.315]    [Pg.317]    [Pg.319]    [Pg.84]    [Pg.48]    [Pg.502]    [Pg.9]    [Pg.872]    [Pg.431]    [Pg.281]    [Pg.26]    [Pg.172]    [Pg.242]    [Pg.172]    [Pg.218]    [Pg.209]    [Pg.221]    [Pg.373]    [Pg.3080]    [Pg.133]    [Pg.368]    [Pg.31]    [Pg.297]    [Pg.544]    [Pg.79]    [Pg.255]    [Pg.474]    [Pg.218]    [Pg.229]    [Pg.124]    [Pg.659]    [Pg.219]    [Pg.146]    [Pg.213]    [Pg.634]    [Pg.155]    [Pg.217]    [Pg.488]   


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Dispersion assessment

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