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Adsorption surface charge

The effect of adsorption surface charging on electrophysical characteristics of polycrystalline semiconductor adsorbents... [Pg.51]

In addition to these chemical reactions described above, many physical parameters need to be considered as well in terms of post-CMP cleaning. Extensive investigations have been conducted on the correlations between post-CMP cleaning efficiency and relevant physical forces such as the van der Waals force, electrostatic force, particle adhesion, chemical adsorption, surface charge modification, and wettability. It is expected that these factors strongly influence the particle-removal capability of post-CMP cleaning solution. [Pg.478]

Molecular structure/biospecific adsorption Surface charge/ionic binding Metals complex formation/coordination complex Molecular size and shape/size exclusion Hydrophobicity/hydrophobic complex formation... [Pg.53]

Figure V-8 illustrates that there can be a pH of zero potential interpreted as the point of zero charge at the shear plane this is called the isoelectric point (iep). Because of specific ion and Stem layer adsorption, the iep is not necessarily the point of zero surface charge (pzc) at the particle surface. An example of this occurs in a recent study of zircon (ZrSi04), where the pzc measured by titration of natural zircon is 5.9 0.1... Figure V-8 illustrates that there can be a pH of zero potential interpreted as the point of zero charge at the shear plane this is called the isoelectric point (iep). Because of specific ion and Stem layer adsorption, the iep is not necessarily the point of zero surface charge (pzc) at the particle surface. An example of this occurs in a recent study of zircon (ZrSi04), where the pzc measured by titration of natural zircon is 5.9 0.1...
A quantitative treatment for the depletive adsorption of iogenic species on semiconductors is that known as the boundary layer theory [84,184], in which it is assumed that, as a result of adsorption, a charged layer is formed. Doublelayer theory is applied, and it turns out that the change in surface potential due to adsorption of such a species is proportional to the square of the amount adsorbed. The important point is that very little adsorption, e.g., a 0 of about 0.003, can produce a volt or more potential change. See Ref. 185 for a review. [Pg.718]

An additional method for increasing particle size deserves mention. When a precipitate s particles are electrically neutral, they tend to coagulate into larger particles. Surface adsorption of excess lattice ions, however, provides the precipitate s particles with a net positive or negative surface charge. Electrostatic repulsion between the particles prevents them from coagulating into larger particles. [Pg.242]

In adsorptive stripping voltammetry the deposition step occurs without electrolysis. Instead, the analyte adsorbs to the electrode s surface. During deposition the electrode is maintained at a potential that enhances adsorption. For example, adsorption of a neutral molecule on a Hg drop is enhanced if the electrode is held at -0.4 V versus the SCE, a potential at which the surface charge of mercury is approximately zero. When deposition is complete the potential is scanned in an anodic or cathodic direction depending on whether we wish to oxidize or reduce the analyte. Examples of compounds that have been analyzed by absorptive stripping voltammetry also are listed in Table 11.11. [Pg.519]

Soluble Salt Flotation. KCl separation from NaCl and media containing other soluble salts such as MgCl (eg, The Dead Sea works in Israel and Jordan) or insoluble materials such as clays is accompHshed by the flotation of crystals using amines as coUectors. The mechanism of adsorption of amines on soluble salts such as KCl has been shown to be due to the matching of coUector ion size and lattice vacancies (in KCl flotation) as well as surface charges carried by the soflds floated (22). Although cation-type coUectors (eg, amines) are commonly used, the utUity of sulfonates and carboxylates has also been demonstrated in laboratory experiments. [Pg.51]

Electrostatic Interaction. Similarly charged particles repel one another. The charges on a particle surface may be due to hydrolysis of surface groups or adsorption of ions from solution. The surface charge density can be converted to an effective surface potential, /, when the potential is <30 mV, using the foUowing equation, where -Np represents the Faraday constant and Ai the gas law constant. [Pg.544]

Surface Modification. Reaction or adsorption at the soHd surface can alter its properties and lead to a surface charge or steric stabilization... [Pg.546]

The size of particles removed by such filters is less than the size of the passages. The mechanism of removal includes adsorption (qv) of the impurities at the interface between the media and the water either by specific chemical or van der Waals attractions or by electrostatic interaction when the medium particles have surface charges opposite to those on the impurities to be removed. [Pg.276]

A good example of a surface-modified lens is the Sola/Bames-Hind Hydrocurve Flite lens, introduced in 1986. The material for the commercial Hydrocurve lens, bufilcon A [56030-52-5] contains methacrylic acid and has a high affinity for protein and subsequent deposition. The surface of the Flite lens was chemically modified with the addition of diazomethane (190) to reduce the surface charge. In vitro testing demonstrated a decrease in protein adsorption (191). [Pg.107]

At positive surface charge density, the CP density exhibits a large maximum at a very short distance from the electrode. The position of this maximum is closer to the electrode than that of the first water layer, thus giving a,clear indication of contact adsorption of this anion. The Na" ... [Pg.366]

The capacitance is a readily measured interfacial property and it gives qualitative information on the adsorption of species at the electrode surface. Since the surface charge density, q, is a function of the potential and of coverage, the measured capacitance may be expressed as the sum of a true (high frequency) capacitance and an adsorption pseudocapacitance, i.e. q f(E,6) and hence... [Pg.167]

A question of practical interest is the amount of electrolyte adsorbed into nanostructures and how this depends on various surface and solution parameters. The equilibrium concentration of ions inside porous structures will affect the applications, such as ion exchange resins and membranes, containment of nuclear wastes [67], and battery materials [68]. Experimental studies of electrosorption studies on a single planar electrode were reported [69]. Studies on porous structures are difficult, since most structures are ill defined with a wide distribution of pore sizes and surface charges. Only rough estimates of the average number of fixed charges and pore sizes were reported [70-73]. Molecular simulations of nonelectrolyte adsorption into nanopores were widely reported [58]. The confinement effect can lead to abnormalities of lowered critical points and compressed two-phase envelope [74]. [Pg.632]


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See also in sourсe #XX -- [ Pg.394 ]




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