Water testing alkalinity

The four samples from each location were (1) nonfiltered, nonstabilized water for alkalinity testing, (2) field-filtered, nonstabilized water for nitrate and chloride testing, (3) field-filtered water stabilized with nitric acid for calcium, magnesium, and sodium testing, and (4) field-filtered water stabilized with sulfuric acid for ammonia and phosphate testing. 

Bicarbonate and carbonate ions are common OH scavengers that exist in equilibrium in natural waters and react with OH with second-order rate constants of 8.5 x 106 and 3.9 x 108 Mr1 s respectively. Of the waters tested, potable water had a pH of about 7 and secondary wastewater a pH of about 9. As the pH increased, OH scavenging increased due to the presence of increased alkalinity species, bicarbonate and carbonate ions, thereby reducing removal efficiency. The effect of these ions on OH can be predicted according to the reactions ... 

If the water is first concentrated to one-fiftieth of its bulk, tests may be carried out for magnesia and phosphates. The former is precipitated as magnesium ammonium phosphate on standing for some twenty-four hours after addition of sodium phosphate solution to the water rendered alkaline with ammonium hydroxide in the presence of chloride. It is assumed that any lime has previously been removed with ammonium oxalate. Phosphates are precipitated as yellow phosphomolybdate on adding excess of ammonium molybdate solution to the water acidified with nitric acid, and warming. 

Use may be made of the intermediate formation of acetone dicarboxylic acid and of the interaction of the latter with sodium nitroprusside solution to yield a red colouration as a test for citrates. When about 0-5 g of a citrate or of citric acid is treated with 1 ml concentrated sulphuric acid for 1 minute, the mixture cooled, cautiously diluted with water, rendered alkaline with sodium hydroxide solution and then a few millilitres of a freshly prepared solution of sodium nitroprusside added, an intense red colouration results. 

Ba, Sr, and B. Consistency between programs was evaluated by comparing the log of the molal concentrations of free ions and complexes for two test solutions a hypothetical seawater analysis and a hypothetical river water analysis. Comparison of the free major ion concentrations in the river water test case shows excellent agreement for the major species. In the seawater test case there is less agreement and for both test cases the minor species commonly show orders of magnitude differences in concentrations. These differences primarily reflect differences in the thermodynamic data base of each chemical model although other factors such as activity coefficient calculations, redox assumptions, temperature corrections, alkalinity corrections and the number of complexes used all have an affect on the output. 

Place in an eight-inch tube 5 ml of the unsaturated hydrocarbon and 5 ml of cold 70 per cent sulfuric acid. Cool the mixture in tap water, place a solid rubber stopper in the mouth of the tube, and shake with cooling until the hydrocarbon dissolves and a clear liquid results. Add 6 g of ammonium sulfate dissolved in 8 ml of water. Insert the separatory stopper, and remove the aqueous acid layer. The liquid which is left in the reaction tube can be tested with bromine water or alkaline permanganate to show that it is not an olefin. If it is desired to purify the alcohol, add 1 g of anhydrous calcium sulfate and shake from time to time over a period of fifteen minutes. Pour the crude alcohol into a distilling tube. Heat with a small flame and collect the proper fraction. If amylene is used, and the water is not completely removed by the drying agent, a constant boiling mixture will be formed which boils at 87°. 

Nitrc Iycerine should form a clear, or very slightly turbid, pale yellow liquid. The moisture is estimated by allowing to stand over calcium chloride (not sulphuric acid) in the cold. Nitroglycerine should be practically free from acidity and alkalinity to test for these, 20 g. is shaken with 0 c.c. of water and the water tested with litmus and if necessary titrated, using methyl orange as indicator. 

Methods of analysis (ASTM D-128, IP 37) are available for the measurement of excessive acidity derived from oxidation. These methods cover conventional grease that consists essentially of petroleum oil and soap. Thus these test methods are applicable to many types but not all grease. The constituents covered by the test series are soap, unsaponifiable matter (base oil), water, free alkalinity, free fatty acid, fat, glycerin, and insoluble. A supplementary test method is also provided and is intended for application to grease that contains thickeners that are essentially insoluble in n-hexane and to grease that cannot be analyzed by conventional methods because of the presence of such constituents as nonpetroleum fluids or nonsoap-type thickeners, or both. These methods may not be applicable to grease analysis when lead, zinc, or aluminum soaps are present or in the presence of some additives such as sodium nitrite. 

Cement, of course, is by far the most common and best-recognised cause of chromate allergy. Cement contains varying amounts of chromate for instance, Ellis and Freeman (1986) found water-soluble cement in Australia to vary from less than 1 ppm to 124 ppm, with the majority tested showing less than 10 ppm. Cement, on the addition of water, becomes alkaline and is probably a factor in facilitating sensitization to the chromate in cement. This may be the reason why cases of contact dermatitis due to allergy to chromate... 

When determining the amount of the water-soluble alkaline constituents of ashes, it is advisable to shake the ash from about 0.1 g of coal or charcoal for several minutes with 10 ml water allow to stand for 24 hours and then centrifuge. A drop of the solution is then evaporated on a frosted slide and spotted with the reagent. Hard coal and brown coal were found to contain very little soluble alkali, while wood charcoal had a high alkali content. The test may be applied to the rapid examination of small samples of ash... 

Sulphuric add test. Heat 0 5 g. of citric acid or a citrate with 1 ml. of H2SO4 CO and COg are evolved and the mixture turns yellow, but does not char. Acetone dicarboxylic acid, OC(CH2COOH)g, is also formed, and is tested for after heating the mixture for 1 minute cool, add a few ml. of water and make alkaline with NaOH solution. Add a few ml. of a freshly prepared solution of sodium nitroprusside and note the intense red coloration (see Test 4 a) for ketones, p. 346). 

Phthalein reaction. Fuse together carefully in a dry test-tube a few crystals of phthalic acid or of a phthalate and an equal quantity of ph tol moistened with 2 drops of cone. H2SO4. Cool, dissolve in water and add NaOH solution in excess the bright red colour of phenolphthalein in alkaline solution is produced. 

Ltease test. The enzyme uretwe hydrolyses urea to ammonium carbonate (p. 519). The reaction is sp ific and is frequently used for solu tions of urea to which the biuret test cannot be applied. Add about 5 drops of phenohred to o 2 g. of urea dissolved in 5 ml. of water. To this yellow solution, add 0 2 g. of jack bean meal suspended in 2 ml. of water containing. also 5 drops of phenol-red. The colour changes to red as the solution becomes alkaline. 

Hydrolysis of benzanilide. Place 5 g. of benzanilide and 50 ml. of 70 per cent, sulphuric acid in a small flask fitted with a reflux condenser, and boU gently for 30 minutes. Some of the benzoio acid will vapourise in the steam and solidify in the condenser. Pour 60 ml. of hot water down the condenser this will dislodge and partially dissolve the benzoic acid. Cool the flask in ice water filter off the benzoic acid (anifine sulphate does not separate at this dilution), wash well with water, drain, dry upon filter paper, and identify by m.p. (121°) and other tests. Render the filtrate alkaline by cautiously adding 10 per cent, sodium hydroxide solution, cool and isolate the aniline by ether extraction. Recover the ether and test the residue for anifine (Section IV,100). 

Methyl p-toluenesulphonate. This, and other alkyl esters, may be prepared in a somewhat similar manner to the n-butyl ester with good results. Use 500 g. (632 ml.) of methyl alcohol contained in a 1 litre three-necked or bolt-head flask. Add 500 g. of powdered pure p-toluene-sulphonyl chloride with mechanical stirring. Add from a separatory funnel 420 g. of 25 per cent, sodium hydroxide solution drop by drop maintain the temperature of the mixture at 23-27°. When all the alkali has been introduced, test the mixture with litmus if it is not alkaline, add more alkali until the mixture is neutral. Allow to stand for several hours the lower layer is the eater and the upper one consists of alcohol. Separate the ester, wash it with water, then with 4 per cent, sodium carbonate solution and finally with water. Dry over a little anhydrous magnesium sulphate, and distil under reduced pressure. Collect the methyl p-toluenesulphonate at 161°/10 mm. this solidifies on cooling and melts at 28°. The yield is 440 g. 

Benzenesulphonyl chloride test. Proceed as in the benzoyl chloride test, but use 15-20 ml. of 5 per cent, sodium hydroxide solution. Examine the product when the odour of the sulphonyl chloride has disappeared. (If no reaction has occurred, the substance is probably a tertiary amine.) If a precipitate appears in the alkaline solution, dilute with about 10 ml. of water and shake if the precipitate does not dissolve, a secondary amine is indicated. If the solution is clear, acidify it cautioiosly to Congo red with dilute hydrochloric acid a precipitate is indicative of a primary amine. 

Hydrolysis of a sulphonamide. Mix 2 g. of the sulphonamide with 3-5 ml. of 80 per cent, sulphuric acid in a test-tube and place a thermometer in the mixture. Heat the test-tube, with frequent stirring by means of the thermometer, at 155-165° until the solid passes into solution (2-5 minutes). Allow the acid solution to cool and pour it into 25-30 ml. of water. Render the resulting solution alkaline with 20 per cent, sodium hydroxide solution in order to liberate the free amine. Two methods may be used for isolating the base. If the amine is volatile in steam, distil the alkaline solution and collect about 20 ml. of distillate extract the amine with ether, dry the ethereal solution with anhydrous potassium carbonate and distil off the solvent. If the amine is not appreciably steam-volatile, extract it from the alkaline solution with ether. The sulphonic acid (as sodium salt) in the residual solution may be identified as detailed under 13. 

The preferred method of determining water in glycerol is by the Kad Fischer volumetric method (18). Water can also be determined by a special quantitative distillation in which the distilled water is absorbed by anhydrous magnesium perchlorate (19). Other tests such as ash, alkalinity or acidity, sodium chloride, and total organic residue are included in AOCS methods (13,16,18). 

Alkali or alkaline-earth salts of both complexes are soluble in water (except for Ba2[Fe(CN)g]) but are insoluble in alcohol. The salts of hexakiscyanoferrate(4—) are yellow and those of hexakiscyanoferrate(3—) are mby red. A large variety of complexes arise when one or more cations of the alkah or alkaline-earth salts is replaced by a complex cation, a representative metal, or a transition metal. Many salts have commercial appHcations, although the majority of industrial production of iron cyanide complexes is of iron blues such as Pmssian Blue, used as pigments (see Pigments, inorganic). Many transition-metal salts of [Fe(CN)g] have characteristic colors. Addition of [Fe(CN)g] to an unknown metal salt solution has been used as a quaUtative test for those transition metals. 

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