Potassium injection

Desulfurize the flue gas. A whole range of processes have been developed to remove SO, from flue gases, such as injection of limestone into the furnace, absorption into wet limestone after the furnace, absorption into aqueous potassium sulfite after the furnace, and many others.However, the byproducts from many of these desulfurization processes cause major disposal problems. 

The first of these reactions takes place at temperatures of about 150°C, the second reaction proceeds at about 550—660°C. Typical furnaces used to carry out the reaction include cast-iron retorts the Mannheim mechanical furnace, which consists of an enclosed stationary circular muffle having a concave bottom pan and a domed cover and the Laury furnace, which employs a horizontal two-chambered rotating cylinder for the reaction vessel. The most recent design is the Cannon fluid-bed reactor in which the sulfuric acid vapor is injected with the combustion gases into a fluidized bed of salts. The Mannaheim furnace has also been used with potassium chloride as the feed. 

Nutrients are usuaUy added at concentrations ranging from 0.005 to 0.02% by weight (16). In a field appHcation using hydrogen peroxide, nutrients were added to the injected water at the foUowing concentrations 380 mg/L ammonium chloride 190 mg/L disodium phosphate, and 190 mg/L potassium phosphate, the latter used primarily to complex with iron in the formation to prevent decomposition of hydrogen peroxide (24). 

Hot corrosion is a rapid form of attack that is generally associated with alkali metal contaminants, such as sodium and potassium, reacting with sulfur in the fuel to form molten sulfates. The presence of only a few parts per million (ppm) of such contaminants in the fuel, or equivalent in the air, is sufficient to cause this corrosion. Sodium can be introduced in a number of ways, such as salt water in liquid fuel, through the turbine air inlet at sites near salt water or other contaminated areas, or as contaminants in water/steam injections. Besides the alkali metals such as sodium and potassium, other chemical elements can influence or cause corrosion on bucketing. Notable in this connection are vanadium, primarily found in crude and residual oils. 

The need for heating, water washing, and the use of additives must be addressed when moving from the distillates toward the residuals. Fuel contaminants such as vanadium, sodium, potassium, and lead must be controlled to achieve acceptable turbine parts life. The same contaminants also can be introduced by the inlet air or by water/steam injection, and the combined effects from all sources must be considered. 

Fig. 7.3.3 Relationship between the concentration of H2O2 and the peak intensity of luminescence, when 0.2 ml of a H2O2 solution was injected into a mixture of 0.575 ml of 0.1 M potassium phosphate (pH 7.5), 0.025 ml of a solution of Diplocardia luciferin, and 0.2 ml of luciferase solution (0.12 mg). 1 LU = 109 quanta/s. From Bellisario et al., 1972, with permission from the American Chemical Society.

Fig. 7.3.4 Kinetic profiles of the Diplocardia bioluminescence reaction, when Diplocardia luciferase, H2O2, or Diplocardia luciferin was injected last. In each case, 0.1 ml of the last component was injected into 0.9 ml of the mixture of other components, to give the final concentrations Diplocardia luciferase, 0.1 unit/ml Diplocardia luciferin, 32 mM and H2O2, 32 mM, in 0.1 M potassium phosphate buffer, pH 7.5. From Rudie et al., 1981, with permission from the American Chemical Society.

Concentrated potassium solutions are for IV mixtures only and should never be used undiluted. Direct IV injection of potassium could result in sudden death. When potassium is given IV, it is always diluted in 500 to 1000 mL of an IV solution. The maximum recommended concentration of potassium is 80 mEq in 1000 mL of IV solution (although in acute emergency situations a higher concentration of potassium maybe required). 

FIGURE 5-17 Flow injection potentiometric determination of potassium in serum. (Reproduced with permission from reference 47.)... 

Ny lon-6 (108 g) carpet backed with calcium-carbonate-filled latex and polypropylene was charged to a 1000-mL three-neck round-bottom flask (equipped with a condenser) with 6 mL of 85% phosphoric acid. Superheated steam was injected continuously during a 45-min period. The vapor temperature of the reaction medium was 250-300°C. The volume of distillate collected was 1065 mL. The distillate contained 1.9% e-caprolactam (as determined by GC), which corresponded to a crude yield of 37.5%. The distillate was fractionated in a distillation column and the nonaqueous phase removed. The remaining aqueous phase was treated with 2% potassium permanganate at 40-50°C for 2 h. Evaporation of... 

Kinetic measurements were performed on a Hitachi 150-20 UV/VIS spectrophotometer. Dehydrobrominations were studied in DMF solution using cyclohexyl amine (CHA) as the base. Applied CHA concentrations were 2, 2.5, 3, 3.5, 4 and 5 10 3 mole.dm-3, initial concentration of 1 was 5 10 5 mole.dm-3 in every case (pseudo-first-order conditions). Ionic strength was adjusted to lO l mole.dm 3 with potassium nitrate. Kinetic curves / D(t) / were recorded at fix wavelength, X = 290 ran and the temperature was maintained at 30, 35.5, 40°C. Stock solutions were made daily for la and freshly for every measurement of Ih. The reaction was started by injection of solution of 1 to the thermostated solution of CHA. 

Sometimes it may become necessary to shut-in a gas well when the demand for gas is low. In such instances, the well is shut-in for an indefinite period, after which it is reopened and production is resumed. It often has been found that the production rate of gas from the reopened well is substantially less than it was before the well was shut-in. During production, the inner wall of the production tubing will be coated with a film of condensed freshwater because of the geothermal gradient. This water flows down when production is interrupted and can cause formation damage. This may occur because clays are normally saturated with brine water and not with freshwater. This swelling can be prevented with the injection of some additive, for example, sodium chloride, potassium chloride, calcium chloride, or an alcohol or a similar organic material [1853]. 

The concentration of chlorine dioxide, chlorite and total oxidants was determined on site using a portable colorimeter (Palintest Photometer 5000) and a modification of the DPD test in which any chlorine species are complexed with glycine to ensure only chlorine dioxide reacts with DPD. The chlorite and total oxidants are then determined on a fresh sample by acidification and neutralisation in the presence of potassium iodide. The initial dose level was set at 0.3ppm chlorine dioxide injected in the water feed to the cold... 

It is important that injectable solutions that are to be given intravenously are isotonic, or nearly so. Because of osmotic pressure changes and the resultant exchange of ionic species across red blood cell membranes, nonisotonic solutions, particularly if given in quantities larger than 100 mL, can cause hemolysis or cre-nation of red blood cells (owing to hypotonic or hypertonic solutions, respectively). Dextrose, sodium chloride, or potassium chloride is commonly used to achieve isotonicity in a parenteral formula. 

Earlier corrosion inhibitors limited the maximum strength of the acid to 15% by weight. Improved corrosion inhibitors (see below) have made the use of higher acid concentrations, such as 28% HCl more common. More dilute solutions may initially be injected in sandstone acidizing to reduce the formation of insoluble sodium and potassium fluorosilicates by displacing saline formation water before injection of hydrochloric acid. 

The addition of potassium hydroxide to injection waters has been used to stabilize clays and maintain injectivity (158). Some degree of permanence appears to result from this treatment since injectivity appeared to be substantially maintained during subse-quent injection of low salinity water. 

Gotti et al. [42] reported an analytical study of penicillamine in pharmaceuticals by capillary zone electrophoresis. Dispersions of the drug (0.4 mg/mL for the determination of (/q-penicillaminc in water containing 0.03% of the internal standard, S -met hy I - r-cystei ne, were injected at 5 kPa for 10 seconds into the capillary (48.5 cm x 50 pm i.d., 40 cm to detector). Electrophoresis was carried out at 15 °C and 30 kV, with a pH 2.5 buffer of 50 mM potassium phosphate and detection at 200 rnn. Calibration graphs were linear for 0.2-0.6 pg/mL (detection limit = 90 pM). For a more sensitive determination of penicillamine, or for the separation of its enantiomers, a derivative was prepared. Solutions (0.5 mL, final concentration 20 pg/mL) in 10 mM phosphate buffer (pH 8) were mixed with 1 mL of methanolic 0.015% 1,1 -[ethylidenebis-(sulfonyl)]bis-benzene and, after 2 min, with 0.5 mL of pH 2.5 phosphate buffer. An internal standard (0.03% tryptophan, 0.15 mL) was added and aliquots were injected. With the same pH 2.5 buffer and detection at 220 nm, calibration graphs were linear for 9.3-37.2 pg/mL, with a detection limit of 2.5 pM. For the determination of small amounts of (L)-penicillamine impurity, the final analyte concentration was 75 pg/mL, the pH 2.5 buffer contained 5 mM beta-cyclodextrin and 30 mM (+)-camphor-10-sulfonic acid, with a voltage of 20 kV, and detection at 220 nm. Calibration graphs were linear for 0.5-2% of the toxic (L)-enantiomer, with a detection limit of 0.3%. 

MWNTs favored the detection of insecticide from 1.5 to 80 nM with a detection limit of InM at an inhibition of 10% (Fig. 2.7). Bucur et al. [58] employed two kinds of AChE, wild type Drosophila melanogaster and a mutant E69W, for the pesticide detection using flow injection analysis. Mutant AChE showed lower detection limit (1 X 10-7 M) than the wild type (1 X 10 6 M) for omethoate. An amperometric FIA biosensor was reported by immobilizing OPH on aminopropyl control pore glass beads [27], The amperometric response of the biosensor was linear up to 120 and 140 pM for paraoxon and methyl-parathion, respectively, with a detection limit of 20 nM (for both the pesticides). Neufeld et al. [59] reported a sensitive, rapid, small, and inexpensive amperometric microflow injection electrochemical biosensor for the identification and quantification of dimethyl 2,2 -dichlorovinyl phosphate (DDVP) on the spot. The electrochemical cell was made up of a screen-printed electrode covered with an enzymatic membrane and combined with a flow cell and computer-controlled potentiostat. Potassium hexacyanoferrate (III) was used as mediator to generate very sharp, rapid, and reproducible electric signals. Other reports on pesticide biosensors could be found in review [17],... 

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