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Exchangeable Bases

More substitution takes place than shown Na 33 or 33 refers to the exchangeable base (cation) of which 0.33 equivalent is a typical value. [Pg.197]

SEPARATION OF HEAVY METALS IN AQUEOUS SOLUTIONS BY A NEW ION EXCHANGER BASED ON CELLULOSE... [Pg.289]

Typical Transfer Coefficients For Air-Cooied Exchangers Based on Outside Bare Tube Surface... [Pg.37]

Ratnam and Patwardhan present graphs to aid in analyzing multipass exchangers, based on equations developed. Turton, et al. also presents performance and design charts based on TEMA charts (Figure 10-34J) and combining these with Temperature Efficiency Charts from TEMA (Figures 10-35A-C). [Pg.72]

Hardness breakthrough with ion-exchange (base exchange, BX) softening NOTE Caused by Fe/Mn fouling, resin breakdown/loss, or inadequate regeneration. Increased risk of carbonate scale or phosphate sludge Loss of alkalinity and hence an increased silica deposition risk... [Pg.202]

Chironomus parvae salivary eland cells Na liquid membrane micropipet [ion-exchanger based on tetra(-p-chloro-phenyl)borate] Na 16 mM 149 ... [Pg.13]

Ionic solutes can be separated by ion-exchange chromatography using microparticulate resins or bonded ion-exchangers based on microparticulate silica. Such separations are often achieved more easily by ion-suppression or ion-pairing techniques, which use bonded phase columns in the reverse phase mode. [Pg.122]

Dynamic parameters for heterogeneous systems have been explored in the liquid, liquid like, solid like, and solid states, based on analyses of the longitudinal or transverse relaxation times, chemical exchange based on line-shape analysis and separated local field (SLF), time domain 1H NMR, etc., as summarized in Figure 3. It is therefore possible to utilize these most appropriate dynamic parameters, to explore the dynamic features of our concern, depending upon the systems we study. [Pg.8]

Micro heat exchangers based on microchannel architecture. Top left and bottom Reprinted with permission from W. Ehrfeld et al., Microreactors New Technology for Modern Chemistry. Wiley-VCH Weinheim, Germany, 2000. Top right Courtesy of the Institut fuer Mikrotechnik Mainz, GmbH. [Pg.38]

Ion-exchange chromatography (both cation and anion) can also be undertaken in HPLC format. Though not as extensively employed as reverse-phase or size-exclusion systems, ion-exchange-based systems are of use in analysing for impurities unrelated to the product, as well as detecting and quantifying deamidated forms. [Pg.184]

The line-broadening data as a function of pH, typically shown for the W(IV) in Figs. 13 and 14, incorporating the known pKa values (Table II), were fitted in 5 X 5 Kubo-Sack matrices describing the exchange based on the above schemes (6, 57). The experimentally determined chemical shift and linewidth data in the absence of exchange for the aqua oxo, hydroxo oxo, and dioxo species and the pH-dependent species distribution as calculated from the acid dissociation constants for the four systems were all introduced in the different matrices and the spectra were computer simulated. For each set of chosen rate con-... [Pg.85]

US stock exchanges based on the probabilistic approach, requiring the report of only proved reserves they, nonetheless, also allow scope for some discretion. In conclusion, it can be said that, so far, there are no international requirements or standards in place regarding reserve classification and reporting, and the methodologies used for reserve estimates seem to vary according to their purpose as a result, reserve data are often referred to as political data . The consequences are inconsistency and controversy about the future supply of oil and gas. [Pg.56]

Brasuel M, Kopelman R, Miller TJ, Tjalkens R, Philbert MA (2001) Fluorescent nanosensors for intracellular chemical analysis decyl methacrylate liquid polymer matrix and ion-exchange-based potassium PEBBLE sensors with real-time application to viable rat C6 glioma cells. Anal Chem 73 2221-2228... [Pg.224]

Fig. 12.6 Identification of the residues undergoing conformational exchange based on the field dependence of relaxation parameters a the comparison of 2R 2-R ] values measured at three fields, 9.4, 11.7, and 14.1 T (shown as grey, white, and black bars, respectively) b the values of Rex + 2czJ(0) at 500 MHz directly derived from the difference between the 2R 2-R values (Eq. (17)) at 600 and 500 MHz (as described in Ref. [16]). This analysis does not require structural information. A strong increase in 2R 2—R] with the field in panel a could be indicative of the conformational exchange, as further quantified in b. Although the contributions from CSA and R cannot be sepa-... Fig. 12.6 Identification of the residues undergoing conformational exchange based on the field dependence of relaxation parameters a the comparison of 2R 2-R ] values measured at three fields, 9.4, 11.7, and 14.1 T (shown as grey, white, and black bars, respectively) b the values of Rex + 2czJ(0) at 500 MHz directly derived from the difference between the 2R 2-R values (Eq. (17)) at 600 and 500 MHz (as described in Ref. [16]). This analysis does not require structural information. A strong increase in 2R 2—R] with the field in panel a could be indicative of the conformational exchange, as further quantified in b. Although the contributions from CSA and R cannot be sepa-...
The design of fixed-bed ion exchangers shares a common theory with fixed-bed adsorbers, which are discussed in Chapter 17. In addition, Thomas(14) has developed a theory of fixed-bed ion exchange based on equation 18.21. It assumed that diffusional resistances are negligible. Though this is now known to be unlikely, the general form of the solutions proposed by Thomas may be used for film- and pellet-diffusion control. [Pg.1069]

By treating Nafion (NR-50), a perfluorinated acidic ion exchanger based on sulfonic acid groups, with scandium(III) chloride hexahydrate Kobayashi et al. generated a solid scandium-derived catalyst (29) (Nafion-Sc) that proved to be effective in al-lylation reactions of carbonyl compounds with tetraallyltin (Scheme 4.15). Since the catalyst is stable in both organic solvents and water, even unprotected carbohydrates could be transformed directly in aqueous solvents. The resulting homo-allylic alcohols were separated by simple filtration [97]. [Pg.219]

Higher rates of horizontal gene exchange, based on the abundant presence of plasmid transfer (Tra), plasmid mobilization (Mob), transposons (Tn), insertion seqnences (IS), and similar fnnctions or elements, seem to be a rule in these variable gene pools. [Pg.20]

Development of methods related to DFT that can treat this situation accurately is an active area of research where considerable progress is being made. Two representative examples of this kind of work are P. Rinke, A. Qteish, J. Neugebauer, and M. Scheffler, Exciting Prospects for Solids Exact Exchange Based Functional Meet Quasiparticle Energy Calculations, Phys. Stat. Sol. 245 (2008), 929, and J. Uddin, J. E. Peralta, and G. E. Scuseria, Density Functional Theory Study of Bulk Platinum Monoxide, Phys. Rev. B, 71 (2005), 155112. [Pg.29]

The TEB value may be obtained by either the sum of the individually measured cations or by evaporating and igniting a portion of the ammonium ethanoate leachate to convert the metallic cations to oxides and carbonates, followed by addition of excess acid (to convert carbonates to chlorides) and back-titration with alkali. The latter method is difficult if the soil is insufficiently base-rich to provide an adequate amount of bases for the titration. On the other hand, the calcium carbonate in calcareous soils may be partially leached by the ammonium ethanoate at pH 7.0 in addition to the exchangeable bases and thus give an exaggerated TEB value and a percentage base saturation in excess of 100%. The TEB by ignition/titration can serve as a check on the values from the summation method. [Pg.60]


See other pages where Exchangeable Bases is mentioned: [Pg.418]    [Pg.35]    [Pg.489]    [Pg.421]    [Pg.421]    [Pg.550]    [Pg.289]    [Pg.257]    [Pg.161]    [Pg.274]    [Pg.13]    [Pg.730]    [Pg.908]    [Pg.889]    [Pg.104]    [Pg.110]    [Pg.64]    [Pg.183]    [Pg.81]    [Pg.190]    [Pg.191]    [Pg.235]    [Pg.124]    [Pg.59]    [Pg.62]   


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1.2.3- Thiadiazoles, base-catalyzed exchange

1.3.4- Thiadiazole, base-catalyzed exchange

Acid-Base Properties of Cation-Exchanged Montmorillonites

Acid-base exchange

Anion exchange membrane-based direct

Anion exchanger silica-based

Anion exchangers polymer-based

Anion-exchange reactions Lewis-acid-based

Base exchange

Base exchange enzyme

Base exchange process

Base exchange reaction

Base exchange synthetic

Base exchanging capacity

Base hydrolysis proton exchange

Base-Catalyzed Exchange

Base-catalysed H-D exchange

Base-catalysed hydrogen exchange

Base-catalysed mechanisms exchange

Base-catalyzed H-D exchange

Base-catalyzed hydrogen exchange

Base-catalyzed hydrogen exchange rates

Base-catalyzed hydrogen isotope exchange

Base-exchange materials

Base-exchange softening

Boundary based exchange symmetry theory

Catalysis base-catalyzed exchange

Cation exchange capacity, exchangeable bases and base saturation

Cation exchange polymer-based materials

Cation exchange silica-based materials

Commercial cation exchanger based

Cracking catalysts base exchanging properties

Exchange reactions, base catalyzed

Exchange reactions, base catalyzed mechanism

Exchange without Added Acid or Base

Exchange-based options

Faujasite base exchanged

Genetic single base exchange

Hard soft acid-base exchange reactions

Hard soft acid-base exchange reactions principle

Hard soft acid-base exchange reactions reaction hardness

Heat Exchanger Network Design Based on the Optimization of Reducible Structure

High-temperature proton exchange acid-base polymer membrane

Homogeneous catalysis base-catalyzed exchange

Hydrocarbon polymers proton exchange membranes based

Hydrogen exchange base catalysis

Hydrogen exchange base-catalyzed, stereochemistry

Hydrogen exchange, base-catalyzed 1,2,4-triazines

Hydrogen exchange, base-catalyzed azoles

Hydrogen exchange, base-catalyzed azolium ions

Hydrogen-deuterium exchange, base

Hydrogen-deuterium exchange, base catalyzed

Ion-exchanger-based ISEs

Kinetic treatment based on exchange current

Ligation of zeolite exchanged transition ions with Schiff base-type ligands

Mannich bases amine exchange reactions

Phospholipid base-exchange reaction

Polymer-Based Cation Exchangers

Proton exchange membrane -based

Proton exchange membrane -based direct methanol fuel cell

Proton exchange, acid- base

Pyridazine 1-oxides base-catalyzed hydrogen-exchange

Pyridazines base-catalyzed hydrogen exchange

Pyrimidines base-catalyzed hydrogen exchange

Reactions catalysed by organic polymer-based cation exchangers

Serine base-exchange

Silica-Based Cation Exchangers

Solid polymer electrolytes cation exchange membrane-based

Strong base anion-exchange resins

Strong-base anion exchangers

Strong-base ion exchange

Turbidity base exchange

Water treatment base exchange

Weak base anion-exchangers

Weak base ion exchange

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