Potassium® ion

Leigh D A, Moody A E, Wade F A, King T A, West D and Bahra G S 1995 Second harmonic generation from Langmuir-Blodgett films of fullerene-aza-crown ethers and their potassium ion complexes Langmuir 11 2334-6... 

The ability of living organisms to differentiate between the chemically similar sodium and potassium ions must depend upon some difference between these two ions in aqueous solution. Essentially, this difference is one of size of the hydrated ions, which in turn means a difference in the force of electrostatic (coulombic) attraction between the hydrated cation and a negatively-charged site in the cell membrane thus a site may be able to accept the smaller ion Na (aq) and reject the larger K (aq). This same mechanism of selectivity operates in other ion-selection processes, notably in ion-exchange resins. 

The metal-ion complexmg properties of crown ethers are clearly evident m their effects on the solubility and reactivity of ionic compounds m nonpolar media Potassium fluoride (KF) is ionic and practically insoluble m benzene alone but dissolves m it when 18 crown 6 is present This happens because of the electron distribution of 18 crown 6 as shown m Figure 16 2a The electrostatic potential surface consists of essentially two regions an electron rich interior associated with the oxygens and a hydrocarbon like exterior associated with the CH2 groups When KF is added to a solution of 18 crown 6 m benzene potassium ion (K ) interacts with the oxygens of the crown ether to form a Lewis acid Lewis base complex As can be seen m the space filling model of this... 

The partitioning of the potassium ion between the resin and solution phases is described by the concentration distribution ratio, D ... 

Prussian Blue. Reaction of [Fe(CN)3] with an excess of aqueous h on(Ill) produces the finely divided, intensely blue precipitate Pmssian Blue [1403843-8] (tetrairon(Ill) tris(hexakiscyanoferrate)), Fe4[Fe(CN)3]. Pmssian Blue is identical to Turnbull s Blue, the name which originally was given to the material produced by reaction of [Fe(CN)3] with excess aqueous h on(Il). The soHd contains or has absorbed on its surface a large and variable number of water molecules, potassium ions (if present in the reaction), and h on(Ill) oxide. The h on(Il) centers are low spin and diamagnetic h on(Ill) centers are high spin. Variations of composition and properties result from variations in reaction conditions. Rapid precipitation in the presence of potassium ion affords a colloidal suspension of Pmssian Blue [25869-98-1] which has the approximate composition KFe[Fe(CN)3]. Pmssian Blue compounds are used as pigments in inks and paints and its formation on sensitized paper is utilized in the production of blueprints. 

Sodium and Potassium. Whereas sodium ion is the most abundant cation in the extracellular fluid, potassium ion is the most abundant in the intracellular fluid. Small amounts of K" are requited in the extracellular fluid to maintain normal muscle activity. Some sodium ion is also present in intracellular fluid (see Fig. 5). Common food sources rich in potassium may be found in Table 7. Those rich in sodium are Hsted in Table 8. 

Sodium and potassium ions are actively absorbed from the intestine. As a consequence of the electrical potential caused by transport of these ions, an equivalent quantity of Cf is absorbed. The resulting osmotic effect causes absorption of water (56). 

A variety of shale-protective muds are available which contain high levels of potassium ions (10). The reaction of potassium ions with clay, well known to soil scientists, results in potassium fixation and formation of a less water-sensitive clay. Potassium chloride, potassium hydroxide, potassium carbonate [584-08-7] (99), tetrapotassium pyrophosphate [7320-34-5] (100), and possibly the potassium salts of organic acids, such as potassium acetate [127-08-2] (101) and formate, have all been used as the potassium source. Potassium chloride is generally preferred because of its low cost and availabihty. 

Ammonium chloride [12125-02-9], ammonium sulfate [7783-20-2], and diammonium phosphate [7708-28-0] have also been used for shale stabilization (102,103). Ammonium ions have essentially the same effect on shales as potassium ions but use of ammonium salts is often objectionable because of the alkaline nature of the mud. In the North Sea and northern Europe, where magnesium-bearing salt formations ate encountered, magnesium chloride [7786-30-3] is used, but in the United States it is used only on a small scale. 

Potassium Phosphates. The K2O—P20 —H2O system parallels the sodium system in many respects. In addition to the three simple phosphate salts obtained by successive replacement of the protons of phosphoric acid by potassium ions, the system contains a number of crystalline hydrates and double salts (Table 7). Monopotassium phosphate (MKP), known only as the anhydrous salt, is the least soluble of the potassium orthophosphates. Monopotassium phosphate has been studied extensively owing to its piezoelectric and ferroelectric properties (see Ferroelectrics). At ordinary temperatures, KH2PO4 is so far above its Curie point as to give piezoelectric effects in which the emf is proportional to the distorting force. There is virtually no hysteresis. 

Potassium [7440-09-7] K, is the third, element ia the aLkaU metal series. The name designation for the element is derived from potash, a potassium mineral the symbol from the German name kalium, which comes from the Arabic qili, a plant. The ashes of these plants al qili) were the historical source of potash for preparing fertilisers (qv) or gun powder. Potassium ions, essential to plants and animals, play a key role in carbohydrate metaboHsm in plants. In animals, potassium ions promote glycolysis, Hpolysis, tissue respiration, and the synthesis of proteins (qv) and acetylcholine. Potassium ions are also beheved to function in regulating blood pressure. 

Microorganisms requite several minerals such as ferrous and potassium ions which play important roles in glutamic acid fermentation. Other important culture conditions include regulating aeration stirring. The biosynthesis of L-glutamic acid is performed under regulated aerobic conditions. 

The nickel oxide modification obtained electrochemicaHy in KOH electrolyte contained potassium ion and its nickel oxidation level are higher than that of NiO 5. Conclusions regarding the transitions between the reduced and oxidized products within the two series are that the redox process was not reversible and although the oxidized phases of the P- and the y-nickel hydroxides differ in energy contents, differences in analyses and x-ray patterns are not significant. 

Fig. 4. Schematic of a multisequence biosensor in which the target glucose is first converted to glucose-6-phosphate, G6P, in the test solution by hexokinase. G6P then reacts selectively with glucose-6-phosphate dehydrogenase immobilized on the quartz crystal surface. Electrons released in the reaction then chemically reduce the Pmssian blue film (see Fig. 3), forcing an uptake of potassium ions. The resulting mass increase is manifested as a...

CP has been used as an ion-exchange material to remove radioisotopes, such as Sr, Cs (43) and U (VI) (44) from solution. CP ion-exchange resins have been used to remove calcium ions from blood (45) and calcium, magnesium, and potassium ions from wine (46). A commercial product made using CP, Calci-Bind, has been used for the treatment of kidney stones (47). 

The composition of the Hquid phase during the early hydration of Portiand cements is controlled mainly by the solution of calcium, sulfate, sodium, and potassium ions. Very Httie alumina, siHca, or iron are present in solution. Calcium hydroxide, as calcium oxide, and gypsum, as calcium sulfate, alone have solubihties of about 1.1 and 2.1 g/L at 25°C, respectively. In the presence of alkaHes released in the first 7 min, the composition tends to be governed by the equiHbrium ... 

Continuous polymerization in a staged series of reactors is a variation of this process (82). In one example, a mixture of chloroprene, 2,3-dichloro-l,3-butadiene, dodecyl mercaptan, and phenothiazine (15 ppm) is fed to the first of a cascade of 7 reactors together with a water solution containing disproportionated potassium abietate, potassium hydroxide, and formamidine sulfinic acid catalyst. Residence time in each reactor is 25 min at 45°C for a total conversion of 66%. Potassium ion is used in place of sodium to minimize coagulum formation. In other examples, it was judged best to feed catalyst to each reactor in the cascade (83). 

Figure 12.11 Schematic diagram of the ion pore of the K+ channel. From the cytosolic side the pore begins as a water-filled channel that opens up into a water-filled cavity near the middle of the membrane. A narrow passage, the selectivity filter, links this cavity to the external solution. Three potassium ions (purple spheres) bind in the pore. The pore helices (red) are oriented such that their carboxyl end (with a negative dipole moment) is oriented towards the center of the cavity to provide a compensating dipole charge to the K ions. (Adapted from D.A. Doyle et al.. Science 280 69-77, 1998.)...

Fully hydrated potassium ion coordinates about 10-11 molecules of water, whereas sodium coordinates about 16-17 molecules [115]. The ionic mobility of potassium is about 50% greater than that of sodium. In simple terms, this means that more of the water in a potassium-catalyzed resin will be available as free water for viscosity reduction and that movement of water from a glue line into the wood will have less effect in moving the adhesive off of the glue line with it. 

There is probably no better evidence for a template effect than its application directly in the solution of a synthetic problem. Rastetter and PhiUion have utilized a substituted 19-crown-6 compound (shown below in Eq. 2.9) in the formation of macrocyclic lactones. Although there were certain experimental variations and the the possibility of intermolecular potassium ion complexation, the overall formation of lactone was favorable. 

Frensch and Vdgtle have recently appended three crown ether units to the cyclo-triveratrylene unit . Note that Hyatt had previously prepared the open-chained relatives of this structure (see Sect. 7.3 and Eq. 7.6). Whereas Hyatt prepared the cyclo-triveratrylene skeleton and then appended polyethyleneoxy arms to it, Frensch and Vogtle conducted the condensation reaction (formaldehyde/HCl) on the preformed benzocrown. Thus benzo-15-crown-5 was converted into the corresponding tris-crown (IS) (mp 203.5—205.5°) in 4% yield. The yield was somewhat higher for the condensation of benzo-18-crown-6, but in both cases, yield ranges were observed. These species formed 1 3 (ligand/salt) complexes with sodium and potassium ions. 

Various other observations of Krapcho and Bothner-By are accommodated by the radical-anion reduction mechanism. Thus, the position of the initial equilibrium [Eq. (3g)] would be expected to be determined by the reduction potential of the metal and the oxidation potential of the aromatic compound. In spite of small differences in their reduction potentials, lithium, sodium, potassium and calcium afford sufficiently high concentrations of the radical-anion so that all four metals can effect Birch reductions. The few compounds for which comparative data are available are reduced in nearly identical yields by the four metals. However, lithium ion can coordinate strongly with the radical-anion, unlike sodium and potassium ions, and consequently equilibrium (3g) for lithium is shifted considerably... 

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