Aqueous solution conductivity testing

Aqueous solution conductivity is an IPC test used to determine the removal of dissolved ionic impurities (salt) from filter cakes and extractions of product-rich organic phases.The initial water conductivity ( S/cm) is used as the basis for the criteria for IPC. The end point for washes is usually established at a level when the conductivity of the final aqueous extraction(s) and wet cake wash solutions are close to the initial conductivity of the prewash water. 

The need for temperature cycling should be taken into account when designing or conducting tests. The nature of the test vessel should be considered for tests in aqueous solutions at temperatures above about 60°C since soluble constituents of the test vessel material can inhibit or accelerate the corrosion process. An inhibiting effect of soluble species from glass, notably silica, on the behaviour of steel in hot water has been shown . Pure quartz or polymeric materials are often more appropriate for test vessel construction. 

J.9 You are asked to identify compound X, which was extracted from a plant seized by customs inspectors. You run a number of tests and collect the following data. Compound X is a white, crystalline solid. An aqueous solution of X turns litmus red and conducts electricity poorly, even when X is present at appreciable concentrations. When you add sodium hydroxide to the solution a reaction takes place. A solution of the products of the reaction conducts electricity well. An elemental analysis of X shows that the mass percentage composition of the compound is 26.68% C and 2.239% H, with the remainder being oxygen. A mass spectrum of X yields a molar mass of 90.0 g-moF. (a) Write the empirical formula of X. (b) Write... 

The permeability tests for alkali metal ions in the aqueous solution were also conducted. When an aqueous salt solution moves to cell 2 through the membrane from cell 1, the apparent diffusion coefficient of the salt D can be deduced from a relationship among the cell volumes Vj and V2, the solution concentration cx and c2, the thickness of membrane, and time t6 . In Table 12, permeabilities of potassium chloride and sodium chloride through the 67 membrane prepared by the casting polymerization technique from the monomer solution in THF or DMSO are compared with each other and with that the permeability through Visking dialyzer tubing. The... 

They react with a solution of bromine in carbon tetrachloride by substitution and an equivalent quantity of hydrogen bromide is evolved (compare addition with unsaturated compounds). When the test is conducted with bromine water and a dilute aqueous solution of a phmiol, the sim of reaction is the separation of a sparingly soluble bromine substitution product. ... 

Laboratory test data indicate that if the organic chemical is present in a dilute aqueous solution, the dielectric constant will not be dangerously low. Dielectric constants above 30 will generally not lower the conductivity substantially enough to damage the soil. Two criteria need to be met for a liquid to not attack clay liners (a) the solution must contain at least 50% water and (b) no separate phase or organic chemicals should be present. 

Next, a series of runs was conducted to determine the effect of various alkali metal hydroxide additions along with the sponge nickel catalyst. The 50 wt. % sodium hydroxide and 50 wt. % potassium hydroxide caustic solution used in the initial test was replaced with an aqueous solution of the alkali metal hydroxide at the level indicated in Table 2. After the reaction number of cycles indicated in Table 2, a sample was removed for analysis. The conditions and results are shown in Table 2. The results reported in Table 2 show the level of 2° Amine in the product from the final cycle. The level of NPA in all of the mns was comparable to the level observed in the initial test. No significant levels of other impurities were detected. 

To distinguish between strong electrolytes, weak electrolytes and nonelectrolytes, prepare equimolar aqueous solutions of the compounds and test their electrical conductivity. If a compound s solution conducts electricity well, it is a strong electrolyte if its solution conducts electricity poorly, it is a weak electrolyte. A solution of a nonelectrolyte does not conduct electricity at all. 

Preparative Photolysis. The preparative photolysis of an aqueous solution (pH=8.5) of AETSAPPE (2.5 M) was conducted in a 1-inch diameter quartz test tube in a Rayonet Reactor (Southern New England Radiation Co.) fitted with 254 nm lamps. Within two hours the solution gelled and the reaction was terminated. Upon acidification the solution cleared, and the product could be re-precipitated by addition of base. This indicates loss of the thiosulfate functionality. The product was dissolved in dilute HC1, precipitated with acetone, and filtered. This process was repeated three times, and the final precipitate was washed with water. The product (20 to 30 mg) was dried in vacuo for 24 hours and stored in a dessicator until use. Comparison of the13 C NMR spectrum of the product with the starting AETSAPPE 13C NMR spectrum clearly shows that the thiosulfate methylene peak shifted upfield, from 39 ppm to 35 ppm. The complete 13 C NMR and IR analysis of the product were consistent with the disulfide product. Further, elemental analysis of the product confirmed that the product was the desired disulfide product 2-amino (2-hydroxy 3-(phenyl ether) propyl) ethyl disulfide (AHPEPED) Expected C 58.39, H 7.08, N 6.20, S 14.18 actual C 58.26, H 7.22, N 6.06, S 14.28. 

The cracking susceptibility of a micro-alloyed HSLA-100 steel was examined and compared to that of a HY-100 steel in the as-received condition and after heat treatment to simulate the thermal history of a single pass weld. Slow strain rate tensile tests were conducted on samples of these alloys with these thermal histories in an inert environment and in an aqueous solution during continuous cathodic charging at different potentials with respect to a reference electrode. Both alloys exhibited reduced ductilities at cathodic potentials indicating susceptibility to hydrogen embrittlement. The results of these experiments will be presented and discussed in relation to the observed microstructures and fractography. 

Subsequently the ion channel activity was tested by single-channel current measurements using planar lipid bilayers. Single-channel conductances of ca. 55 in 500 mM NaCl and 65 pS in KCl were obtained. The weak ion selectivity was claimed to reflect a slightly larger mobility of K compared to that of Na ion in bulk solution. Therefore a large 7.5-A pore structure in lipid bilayers is assumed to resemble the bulk aqueous solution. 

Chromium tetraphenyl iodide in methyl alcohol or moist chloroform is treated with silver oxide, or the iodide is subjected to electrolysis, using an alcohol solution with a platinum or mercury cathode and a rotating silver anode. One molecule of wTater is removed by drying over calcium chloride. The base forms orange-coloured plates, M.pt. 104° to 105° C. when placed in a bath previously heated to 95° C. It dissolves readily in water or alcohols, is sparingly soluble in chloroform, insoluble in benzene or ether. Measurements of its conductivity in aqueous solution show that it is comparable in strength with the alkali hydroxides, whilst comparative tests in methyl alcohol solution show that it is a stronger base than chromium pentaphenyl hydroxide. It may readily be converted into the chloride, bromide and iodide. 

Initial preparative work with oxynitrilases in neutral aqueous solution [517, 518] was hampered by the fact that under these reaction conditions the enzymatic addition has to compete with a spontaneous chemical reaction which limits enantioselectivity. Major improvements in optical purity of cyanohydrins were achieved by conducting the addition under acidic conditions to suppress the uncatalyzed side reaction [519], or by switching to a water immiscible organic solvent as the reaction medium [520], preferably diisopropyl ether. For the latter case, the enzymes are readily immobilized by physical adsorption onto cellulose. A continuous process has been developed for chiral cyanohydrin synthesis using an enzyme membrane reactor [61]. Acetone cyanhydrin can replace the highly toxic hydrocyanic acid as the cyanide source [521], Inexpensive defatted almond meal has been found to be a convenient substitute for the purified (R)-oxynitrilase without sacrificing enantioselectivity [522-524], Similarly, lyophilized and powered Sorghum bicolor shoots have been successfully tested as an alternative source for the purified (S)-oxynitrilase [525],... 

Oliyai R, Lindenbaum S. Stability testing of pharmaceuticals by isothermal heat conduction calorimetry ampicillin in aqueous solution. Int J Pharm 1991 73(1) 33—36. 

Aqueous solutions of acids and bases can be tested using a conductivity tester. The brightness of the bulb is a clue to the concentration of ions in the solution. Which of these solutions have higher concentrations of ions Which have lower concentrations ... 

You isolate a compound with the formula PtCl4 2KC1. From electrical conductance tests of an aqueous solution of the compound, you find that three ions are present, and you also notice that the addition of AgN03 does not cause a precipitate. Give the formula for this compound that shows the complex ion present. Explain your findings, and name this compound. 

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