Potassium limitation

Tilman, E.A., Tilman, D., Crawley, M.J. and Johnston, A.E. 1999. Biological weed control via nutrient competition. Potassium limitation of dandelions. Ecological Applications 9(1) 103-111. 

Kim BS (2002) Production of medium chain length polyhydroxyalkanoates by fed-batch culture of Pseudomonas oleovorans. Biotechnol Lett 24 125-130 Kim YB, Lenz RW, Fuller RC (1992) Poly(b-hydroxyalkanoate) copolymers containing bromi-nated repeating units produced by Pseudomonas oleovorans. Macromolecules 25 1852-1857 Kim SW, Kim P, Lee HS, Kim IH (1996) High production of poly-beta-hydroxybutyrate (PHB) from Methylobacterium organophilum under potassium limitation. Biotechnol Lett 18 25-30 Kim DY, Kim YB, Rhee YH (1998) Bacterial poly(3-hydroxyalkanoates) bearing carbon-carbon triple bonds. Macromolecules 31 4760-4763... 

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. 

Graphite reacts with alkali metals, for example potassium, to form compounds which are non-stoichiometric but which all have limiting compositions (for example K C) in these, the alkaU metal atoms are intercalated between the layers of carbon atoms. In the preparation of fluorine by electrolysis of a molten fluoride with graphite electrodes the solid compound (CF) polycarbon fluoride is formed, with fluorine on each carbon atom, causing puckering of the rings. 

Sodium and potassium hydroxides. The use of these efficient reagents is generally confined to the drying of amines (soda lime, barium oxide and quicklime may also be employed) potassium hydroxide is somewhat superior to the sodium compound. Much of the water may be first removed by shaking with a concentrated solution of the alkali hydroxide. They react with many organic compounds (e.g., acids, phenols, esters and amides) in the presence of water, and are also soluble in certain organic liquids so that their use as desiccants is very limited... 

Examples of typical packaging labels from reagent grade chemicals. Label (a) provides the actual lot assay for the reagent as determined by the manufacturer. Note that potassium has been flagged with an asterisk ( ) because its assay exceeds the maximum limit established by the American Chemical Society (ACS). Label (b) does not provide assayed values, but indicates that the reagent meets the specifications of the ACS for the listed impurities. An assay for the reagent also is provided. 

Potassium nitrate is being used increasingly on intensive crops such as tomatoes, potatoes, tobacco, leafy vegetables, citms, and peaches. The properties that make it particularly desirable for these crops are low salt index, nitrate nitrogen, favorable N K20 ratio, negligible CU content, and alkaline residual reaction in the soil. The low hygroscopicity of KNO (Table 9) leads to its use in direct appHcation and in mixtures. It is an excellent fertilizer but the high cost of production limits its use to specialty fertilizers. 

Because of the special stabiHty of the hexafluoroarsenate ion, there are a number of appHcations of hexafluoroarsenates. For example, onium hexafluoroarsenates (33) have been described as photoinitiators in the hardening of epoxy resins (qv). Lithium hexafluoroarsenate [29935-35-1] has been used as an electrolyte in lithium batteries (qv). Hexafluoroarsenates, especially alkaH and alkaline-earth metal salts or substituted ammonium salts, have been reported (34) to be effective as herbicides (qv). Potassium hexafluoroarsenate [17029-22-0] has been reported (35) to be particularly effective against prickly pear. However, environmental and regulatory concerns have severely limited these appHcations. 

The degree of duorination can be limited by the thermal stabiUty of the solvent or by its reaction with basic potassium duoride through proton abstraction. Such solvent-derived by-products can subsequentiy react with the starting material and/or main product. 

Bleaches of the simple ammoniacal peroxide type give limited lightening, which can be increased with bleach accelerators or boosters, including one or more per salts such as ammonium, potassium, or sodium persulfate or their combinations. These salts, which are susceptible to decomposition in aqueous solution, are packaged as dry powders and added just before use. In the absence of hydrogen peroxide, however, persulfates do not have any bleaching effect (41). 

A iridine traces in aqueous solution can be determined by reaction with 4-(p-nitroben25l)pyridine [1083-48-3] and potassium carbonate [584-08-7]. Quantitative determination is carried out by photometric measurement of the absorption of the blue dye formed (367,368). Alkylating reagents interfere in the determination. A iridine traces in the air can be detected discontinuously by absorption in Folin s reagent (l,2-naphthoquinone-4-sulfonate) [2066-93-5] (369,370) with subsequent chloroform extraction and hplc analysis of the red dye formed (371,372). The detection limit is ca 0.1 ppm. Nitrogen-specific thermal ionisation detectors can be used for continuous monitoring of the ambient air. 

Iodine is only slightly soluble in water and no hydrates form upon dissolution. The solubiHty increases with temperature, as shown in Table 2 (36). Iodine is soluble in aqueous iodide solutions owing to the formation of polyiodide ions. For example, an equiHbrium solution of soHd iodine and KI H2O at 25°C is highly concentrated and contains 67.8% iodine, 25.6% potassium iodide, and 6.6% water. However, if large cations such as cesium, substituted ammonium, and iodonium are present, the increased solubiHty may be limited, owing to precipitation of sparingly soluble polyiodides. Iodine is also more... 

Diketene is a flammable Hquid with a flash point of 33°C and an autoignition temperature of 275°C. It decomposes rapidly above 98°C with slow decomposition occurring even at RT. The vapors are denser than air (relative density 2.9, air air = 1). The explosive limits in air are 2—11.7 vol % (135). In case of fire, water mist, light and stabilized foam, as well as powder of the potassium or ammonium sulfate-type should be used. Do not use basic extinguisher powders and do not add water to a closed container. 

Several methods have received considerable research attention as alternatives to salt curing. These include use of sodium bisulfite as a disinfectant to allow preservation with or without decreased salt in a brine cure use of disinfectants such as quatenary amines for temporary preservation in direct shipping to the taimery from the packing plant (see Disinfectants and antiseptics) preservation of hides by radiation sterilization (see Sterilization techniques) and substitution of materials such as potassium chloride for sodium chloride. These methods have found only limited commercial success. 

Liquid Metals. If operating temperatures rise above 250—300°C, where many organic fluids decompose and water exerts high vapor pressure, hquid metals have found some use, eg, mercury for limited appHcation in turbines sodium, especially its low melting eutectic with 23 wt % potassium, as a hydrauhc fluid and coolant in nuclear reactors and potassium, mbidium, cesium, and gallium in some special uses. 

O ne. Air pollution (qv) levels are commonly estimated by determining ozone through its chemiluminescent reaction with ethylene. A relatively simple photoelectric device is used for rapid routine measurements. The device is caHbrated with ozone from an ozone generator, which in turn is caHbrated by the reaction of ozone with potassium iodide (308). Detection limits are 6—9 ppb with commercially available instmmentation (309). 

Fig. 10. Effect of potassium on SO2 removal where (—) represents the NSPS limit, and (V) represents LMF4-T, ( ) LMF4-U, and ( ) LMF4-V.

Maleic Anhydride. The ACGIH threshold limit value in air for maleic anhydride is 0.25 ppm and the OSHA permissible exposure level (PEL) is also 0.25 ppm (181). Maleic anhydride is a corrosive irritant to eyes, skin, and mucous membranes. Pulmonary edema (collection of fluid in the lungs) can result from airborne exposure. Skin contact should be avoided by the use of mbber gloves. Dust respirators should be used when maleic anhydride dust is present. Maleic anhydride is combustible when exposed to heat or flame and can react vigorously on contact with oxidizers. The material reacts exothermically with water or steam. Violent decompositions of maleic anhydride can be catalyzed at high temperature by strong bases (sodium hydroxide, potassium hydroxide, calcium hydroxide, alkaU metals, and amines). Precaution should be taken during the manufacture and use of maleic anhydride to minimize the presence of basic materials. 

In the other market areas, lead naphthenates are used on a limited basis in extreme pressure additives for lubricating oils and greases. Sodium and potassium naphthenates are used in emulsiftable oils, where they have the advantage over fatty acid soaps of having improved disinfectant properties. Catalyst uses include cobalt naphthenate as a cross-linking catalyst in adhesives (52) and manganese naphthenate as an oxidation catalyst (35). Metal naphthenates are also being used in the hydroconversion of heavy petroleum fractions (53,54) and bitumens (55). 

NiSO (NH 2 04-6H20, and nickel potassium sulfate [10294-65-2], NiSO -K2S04-6H20, are prepared by crystallizing the individual salts from a water solution. These have limited use as dye mordants and are used in metal-finishing compositions (59). 

Nitroethane. The principal use of nitroethane is as a raw material for synthesis in two appHcations. It is used to manufacture a-methyl dopa, a hypertensive agent. Also, the insecticide 3 -methyl-A/-[(methylcarbamoyl)oxy]thioacetimidate [16752-77-5] can be produced by a synthesis route using nitroethane as a raw material. The first step of this process involves the reaction of the potassium salt of nitroethane, methyl mercaptan, and methanol to form methyl methylacetohydroxamate. Solvent use of nitroethane is limited but significant. Generally, it is used in a blend with 1-nitropropane. 

The second important component is the cooling agent or reactor coolant which extracts the heat of fission for some usefiil purpose and prevents melting of the reactor materials. The most common coolant is ordinary water at high temperature and high pressure to limit the extent of boiling. Other coolants that have been used are Hquid sodium, sodium—potassium alloy, helium, air, and carbon dioxide (qv). Surface cooling by air is limited to unreflected test reactors or experimental reactors operated at very low power. 

Chemical additives for gas-based drilling fluids are limited to surfactants (qv), certain polymers, and occasionally salts such as sodium or potassium chloride. An aqueous solution of the additives is iajected iato the air or gas flow to generate a mist or foam. No additives are used ia dry air or gas drilling operations. Gas-based fluids are not recirculated and materials are added continuously. As the fluid exits the well, air or water vapor escapes to the atmosphere, gas and oil are burned, and water and formation soflds are collected into a pit for later disposal. Stable foams must be destabili2ed to separate the air from the Hquid phase for disposal. 

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