Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Potassium localization

This localization phenomenon has also been shown to be important in a case of catalysis by premicellar aggregates. In such a case [ ] premicellar aggregates of cetylpyridinium chloride (CPC) were shown to enhance tire rate of tire Fe(III) catalysed oxidation of sulphanilic acid by potassium periodate in tire presence of 1,10-phenantliroline as activator. This chemistry provides a lowering of tire detection limit for Fe(III) by seven orders of magnitude. It must also be appreciated, however, tliat such premicellar aggregates of CPC actually constitute mixed micelles of CPC and 1,10-phenantliroline tliat are smaller tlian conventional CPC micelles. [Pg.2593]

Potassium Chloride. The principal ore encountered in the U.S. and Canadian mines is sylvinite [12174-64-0] a mechanical mixture of KCl and NaCl. Three beneficiation methods used for producing fertilizer grades of KCl ate thermal dissolution, heavy media separation, and flotation (qv). The choice of method depends on factors such as grade and type of ore, local energy sources, amount of clay present, and local fuel and water availabiUty and costs. [Pg.232]

Naphtha desulfurization is conducted in the vapor phase as described for natural gas. Raw naphtha is preheated and vaporized in a separate furnace. If the sulfur content of the naphtha is very high, after Co—Mo hydrotreating, the naphtha is condensed, H2S is stripped out, and the residual H2S is adsorbed on ZnO. The primary reformer operates at conditions similar to those used with natural gas feed. The nickel catalyst, however, requires a promoter such as potassium in order to avoid carbon deposition at the practical levels of steam-to-carbon ratios of 3.5—5.0. Deposition of carbon from hydrocarbons cracking on the particles of the catalyst reduces the activity of the catalyst for the reforming and results in local uneven heating of the reformer tubes because the firing heat is not removed by the reforming reaction. [Pg.420]

In the United States, aluminum sulfate is usually produced by the reaction of bauxite or clay (qv) with sulfuric acid (see Sulfuric acid and sulfur trioxide). Bauxite is imported and more expensive than local clay, generally kaolin, which is more often used. Clay is first roasted to remove organics and break down the crystalline stmcture in order to make it more reactive. This is an energy intensive process. The purity of the starting clay or bauxite ore, especially the iron and potassium contents, are reflected in the assay of the final product. Thus the selection of the raw material is governed by the overall economics of producing a satisfying product. [Pg.176]

As shovm above, the attachment of the aromatic ring to the carbon chain bearing the basic nitrogen may be accomplished through an ester or an amide configured in either direction. A simple ether linkage fulfills this function in yet another compound that exhibits local anesthetic activity. Thus, alkylation of the mono potassium salt of hydroquinone with butyl bromide affords the ether (77) alkylation of this with w-C3-chloropropyl)morpholine affords pramoxine (78)... [Pg.18]

Besides sodium channels, other ion channels such calcium- and potassium channels as well as certain ligand-gated channels are affected by local anaesthetics. However, this plays only a minor role for nerve block but may have more impact on adverse effects induced by systemical concentrations of these drags. [Pg.701]

Potassium Channels. Table 1 Human K+ channel auxiliary subunits genes, localization, function, and disorders... [Pg.993]

Voltage-gated potassium (Kv) channels are membrane-inserted protein complexes, which form potassium-selective pores that are gated by changes in the potential across the membrane. The potassium current flow through the open channel follows by the electrochemical gradient as defined by the Nernst equation. In general, Kv channels are localized in the plasma membrane. [Pg.1308]

Such an analysis indicates that the zero-sink assumption must be used with extreme caution if accurate flux calculations are required at the local root level. Potassium, for example, is close to the limiting value of A, for the zero sink assumption to be fulfilled, and simulations with larger roots or larger buffer powers could well lead to inaccurate simulation results. Any zero-sink model involving nitrate should be treated with some suspicion. The zero-sink assumption is also widely used in root architecture models (see later). [Pg.347]

M. C. Drew, Comparison of the effects of a localized supply of phosphate, nitrate, ammonium and potassium on the growth of the seminal root system, and the shoot, in barley. New Pliyiol. 75 479 (1975). [Pg.371]

The sensitivity of Magnetic Resonance (MR) to the local concentration, molecular dynamics and molecular environment of these nuclei make it well suited for the study of deterioration processes in concrete materials. Hydrogen (water), lithium, sodium, chlorine and potassium are all MR sensitive nuclei and play an important role in cement chemistry. The ability of MRI to spatially resolve and non-destructively examine test samples as a function of treatment or exposure has the potential to provide new insight to better understand deterioration mechanisms and mass transport properties of concrete materials. [Pg.285]


See other pages where Potassium localization is mentioned: [Pg.1787]    [Pg.2777]    [Pg.149]    [Pg.233]    [Pg.428]    [Pg.324]    [Pg.280]    [Pg.447]    [Pg.516]    [Pg.518]    [Pg.483]    [Pg.280]    [Pg.295]    [Pg.313]    [Pg.359]    [Pg.699]    [Pg.226]    [Pg.81]    [Pg.94]    [Pg.142]    [Pg.596]    [Pg.178]    [Pg.442]    [Pg.117]    [Pg.443]    [Pg.701]    [Pg.992]    [Pg.1026]    [Pg.1166]    [Pg.1052]    [Pg.70]    [Pg.158]    [Pg.18]    [Pg.41]    [Pg.227]    [Pg.391]    [Pg.200]    [Pg.167]    [Pg.1052]    [Pg.42]   
See also in sourсe #XX -- [ Pg.536 ]




SEARCH



Potassium atom, electron localization

Potassium atom, electron localization function

© 2024 chempedia.info