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Affected Anions

A further problem that may cause contamination of the treated MU water is anion leakage as a result of organic fouling. This significantly affects anion resins, preventing ion removal by ion exchange and thus reducing bed capacity. [Pg.200]

Cimetidine is a non-specific cytochrome P450 isoenzyme inhibitor, but it would seem that in most cases, with the exception of loratadine, these enzyme inhibitory effects do not significantly affect the metabolism of antihistamines. More recent evidence has shown cimetidine can also affect drug transporter proteins, in particular it may inhibit organic cation transporters. However, it probably does not affect anion transporter proteins since it does not affect the plasma pharmacokinetics of fexofenadine, which is a substrate of these transporters. ... [Pg.589]

At potentials positive to the bulk metal deposition, a metal monolayer-or in some cases a bilayer-of one metal can be electrodeposited on another metal surface this phenomenon is referred to as underiDotential deposition (upd) in the literature. Many investigations of several different metal adsorbate/substrate systems have been published to date. In general, two different classes of surface stmetures can be classified (a) simple superstmetures with small packing densities and (b) close-packed (bulklike) or even compressed stmetures, which are observed for deposition of the heavy metal ions Tl, Hg and Pb on Ag, Au, Cu or Pt (see, e.g., [63, 64, 65, 66, 62, 68, 69 and 70]). In case (a), the metal adsorbate is very often stabilized by coadsorbed anions typical representatives of this type are Cu/Au (111) (e.g. [44, 45, 21, 22 and 25]) or Cu/Pt(l 11) (e.g. [46, 74, 75, and 26 ]) It has to be mentioned that the two dimensional ordering of the Cu adatoms is significantly affected by the presence of coadsorbed anions, for example, for the upd of Cu on Au(l 11), the onset of underiDotential deposition shifts to more positive potentials from 80"to Br and CE [72]. [Pg.2753]

As we shall see later, the limitations imposed by most solvents may prevent us from being able to utilise the very strong basic characteristics of some anions. However, at this point it is more useful to consider other factors affecting the strengths of acids. [Pg.87]

Flotation reagents are used in the froth flotation process to (/) enhance hydrophobicity, (2) control selectivity, (J) enhance recovery and grade, and (4) affect the velocity (kinetics) of the separation process. These chemicals are classified based on utili2ation collector, frother, auxiUary reagent, or based on reagent chemistry polar, nonpolar, and anionic, cationic, nonionic, and amphoteric. The active groups of the reagent molecules are typically carboxylates, xanthates, sulfates or sulfonates, and ammonium salts. [Pg.46]

Solvent variation can gready affect the acidity of hydantoins. Although two different standard states are employed for the piC scale and therefore care must be exercised when comparing absolute acidity constants measured in water and other solvents like dimethyl sulfoxide (DMSO), the huge difference in piC values, eg, 9.0 in water and 15.0 in DMSO (12) in the case of hydantoin itself, indicates that water provides a better stabilization for the hydantoin anion and hence an increased acidity when compared to DMSO. [Pg.250]

Eig. 5. Pressure drop as affected by resin type, flow rate, and temperature, where A, B, and C, correspond respectively to acryUc strong base anion exchanger (Amberlite IRA-458), styrenic strong base anion exchanger (Amberlite IRA-402), and styrenic strong acid cation exchanger (Amberlite IR-120), all at 4°C. D represents styrenic strong acid cation resin (Amberlite IR-120) at 50°C (14). To convert kg/(cm -m) to lb/(in. -ft), multiply by 4.33 to convert... [Pg.379]

The efficiency of the weathering of rocks in using carbonic acid produced in the carbon cycle is affected by various hydrologic, environmental, and cultural controls. The fact that the principal anion in fresh surface water worldwide almost always is bicarbonate attests to the overriding importance of this process. Exceptions are systems in which evaporite minerals are available for dissolution by groundwater or where human activities are major sources of sulfate or chloride inflow. [Pg.200]

Polymeric coagulants do not affect pH therefore, the need for supplemental alkalinity, such as lime, caustic, or soda ash, is reduced or eliminated. Polymeric coagulants do not add to the total dissolved soHds concentration, eg, 1 ppm of alum adds 0.45 ppm of sulfate ion (expressed as CaCO ) the reduction ia sulfate can significantly extend the capacity of anion-exchange systems. [Pg.259]

The azo coupling reaction proceeds by the electrophilic aromatic substitution mechanism. In the case of 4-chlorobenzenediazonium compound with l-naphthol-4-sulfonic acid [84-87-7] the reaction is not base-catalyzed, but that with l-naphthol-3-sulfonic acid and 2-naphthol-8-sulfonic acid [92-40-0] is moderately and strongly base-catalyzed, respectively. The different rates of reaction agree with kinetic studies of hydrogen isotope effects in coupling components. The magnitude of the isotope effect increases with increased steric hindrance at the coupler reaction site. The addition of bases, even if pH is not changed, can affect the reaction rate. In polar aprotic media, reaction rate is different with alkyl-ammonium ions. Cationic, anionic, and nonionic surfactants can also influence the reaction rate (27). [Pg.428]

Hplc techniques are used to routinely separate and quantify less volatile compounds. The hplc columns used to affect this separation are selected based on the constituents of interest. They are typically reverse phase or anion exchange in nature. The constituents routinely assayed in this type of analysis are those high in molecular weight or low in volatility. Specific compounds of interest include wood sugars, vanillin, and tannin complexes. The most common types of hplc detectors employed in the analysis of distilled spirits are the refractive index detector and the ultraviolet detector. Additionally, the recent introduction of the photodiode array detector is making a significant impact in the analysis of distilled spirits. [Pg.89]


See other pages where Affected Anions is mentioned: [Pg.272]    [Pg.247]    [Pg.709]    [Pg.247]    [Pg.238]    [Pg.242]    [Pg.242]    [Pg.709]    [Pg.122]    [Pg.246]    [Pg.247]    [Pg.55]    [Pg.57]    [Pg.272]    [Pg.247]    [Pg.709]    [Pg.247]    [Pg.238]    [Pg.242]    [Pg.242]    [Pg.709]    [Pg.122]    [Pg.246]    [Pg.247]    [Pg.55]    [Pg.57]    [Pg.243]    [Pg.193]    [Pg.2751]    [Pg.188]    [Pg.445]    [Pg.925]    [Pg.172]    [Pg.241]    [Pg.775]    [Pg.143]    [Pg.231]    [Pg.34]    [Pg.37]    [Pg.195]    [Pg.207]    [Pg.47]    [Pg.236]    [Pg.61]    [Pg.193]    [Pg.403]    [Pg.498]    [Pg.245]    [Pg.75]    [Pg.317]    [Pg.162]    [Pg.261]   


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