Acid tests

While it is believed that color and smell are good indicative factors in assessment of MIC, relying only on these factors could be very misleading. 

FIGURE 4.35 Bubbling sample (right) containing iron sulfide will produce HjS. The nonbubbling sample (left) is normal rust (iron hydroxide). 

As mentioned earlier, while this test may be useful in assessing the existence of iron sulfide in the corrosion products, it cannot guarantee the existence of SRB. 

---

Sulphuric acid test. Heat 0-5 g, of oxamide with cone. HjSO. CO and COj are evolved. 

Both succinic and phthalic anhydride respond to the hydroxamic acid test (see 5 above). 

Chloroform and iodoform give also sodium formate in this reaction CHCI3 -h 4NaOH = HCOONa -h 3NaCl -f zH O. A portion of the solution, before the addition of the HNO3, should therefore be tested for formic acid (Tests, p. 350) ensure however that the solution is neutralised where necessary during these tests. 

Absolute diethyl ether. The chief impurities in commercial ether (sp. gr. 0- 720) are water, ethyl alcohol, and, in samples which have been exposed to the air and light for some time, ethyl peroxide. The presence of peroxides may be detected either by the liberation of iodine (brown colouration or blue colouration with starch solution) when a small sample is shaken with an equal volume of 2 per cent, potassium iodide solution and a few drops of dilute hydrochloric acid, or by carrying out the perchromio acid test of inorganic analysis with potassium dichromate solution acidified with dilute sulphuric acid. The peroxides may be removed by shaking with a concentrated solution of a ferrous salt, say, 6-10 g. of ferrous salt (s 10-20 ml. of the prepared concentrated solution) to 1 litre of ether. The concentrated solution of ferrous salt is prepared either from 60 g. of crystallised ferrous sulphate, 6 ml. of concentrated sulphuric acid and 110 ml. of water or from 100 g. of crystallised ferrous chloride, 42 ml. of concentrated hydiochloric acid and 85 ml. of water. Peroxides may also be removed by shaking with an aqueous solution of sodium sulphite (for the removal with stannous chloride, see Section VI,12). 

CAUTION. Ethers that have been stored for long periods, particularly in partly-filled bottles, frequently contain small quantities of highly explosive peroxides. The presence of peroxides may be detected either by the per-chromic acid test of qualitative inorganic analysis (addition of an acidified solution of potassium dichromate) or by the liberation of iodine from acidified potassium iodide solution (compare Section 11,47,7). The peroxides are nonvolatile and may accumulate in the flask during the distillation of the ether the residue is explosive and may detonate, when distilled, with sufficient violence to shatter the apparatus and cause serious personal injury. If peroxides are found, they must first be removed by treatment with acidified ferrous sulphate solution (Section 11,47,7) or with sodium sulphite solution or with stannous chloride solution (Section VI, 12). The common extraction solvents diethyl ether and di-tso-propyl ether are particularly prone to the formation of peroxides. 

Add 25 g. of finely-powdered, dry acetanilide to 25 ml. of glacial acetic acid contained in a 500 ml. beaker introduce into the well-stirred mixture 92 g. (50 ml.) of concentrated sulphuric acid. The mixture becomes warm and a clear solution results. Surround the beaker with a freezing mixture of ice and salt, and stir the solution mechanically. Support a separatory funnel, containing a cold mixture of 15 -5 g. (11 ml.) of concentrated nitric acid and 12 -5 g. (7 ml.) of concentrated sulphuric acid, over the beaker. When the temperature of the solution falls to 0-2°, run in the acid mixture gradually while the temperature is maintained below 10°. After all the mixed acid has been added, remove the beaker from the freezing mixture, and allow it to stand at room temperature for 1 hour. Pour the reaction mixture on to 250 g. of crushed ice (or into 500 ml. of cold water), whereby the crude nitroacetanilide is at once precipitated. Allow to stand for 15 minutes, filter with suction on a Buchner funnel, wash it thoroughly with cold water until free from acids (test the wash water), and drain well. Recrystallise the pale yellow product from alcohol or methylated spirit (see Section IV,12 for experimental details), filter at the pump, wash with a httle cold alcohol, and dry in the air upon filter paper. [The yellow o-nitroacetanihde remains in the filtrate.] The yield of p-nitroacetanihde, a colourless crystalline sohd of m.p. 214°, is 20 g. 

Dissolve 36 g. of p-toluidine in 85 ml. of concentrated hydrochloric acid and 85 ml. of water contained in a 750 ml. conical flask or beaker. Cool the mixture to 0° in an ice-salt bath with vigorous stirring or shaking and the addition of a httle crushed ice. The salt, p-toluidine hydrochloride, will separate as a finely-divided crystalline precipitate. Add during 10-15 minutes a solution of 24 g. of sodium nitrite in 50 ml. of water (1) shake or stir the solution well during the diazotisation, and keep the mixture at a temperature of 0-5° by the addition of a httle crushed ice from time to time. The hydrochloride wUl dissolve as the very soluble diazonium salt is formed when ah the nitrite solution has been introduced, the solution should contain a trace of free nitrous acid. Test with potassium iodide - starch paper (see Section IV,60). 

Fuming sulphuric acid test. Place 2 ml. of 20 per cent, fuming sulphuric acid in a dry test-tube, add 0 -5 ml. of the hydrocarbon and shake vigorously. Only the aromatic hydrocarbon dissolves completely heat is evolved, but excessive charring should be absent. 

A. Carry out the following preliminary test. Dissolve a drop or a few small crystals of the compound in 1 ml. of rectified spirit (95 per cent, ethanol) and add 1 ml. of iV hydrochloric acid. Note the colour produced when 1 drop of 5 per cent, ferric chloride solution is added to the solution. If a pronounced violet, blue, red or orange colour is produced, the hydrox amic acid test described below is not applicable and should not be used. 

The polyhydric alcohols of Solubility Group II are liquids of relatively high boiling point and may be detected inter alia by the reactions already described for Alcohols (see 6). Compounds containing two hydroxyl groups attached to adjacent carbon atoms (1 2-glyeols), a-hydroxy aldehydes and ketones, and 1 2-diketones may be identified by the periodic acid test, given in reaction 9. 

Working-Capital Ratios Financial analysts make extensive use of ratios in assessing the economic health of a company. For evaluating the ability of a company to successfully maintain and develop its immediate business activities, analysts apply a current ratio and a quick (or acid-test) ratio, as given by... 

Saure-lostmg,/. solution of an acid, -maschine, /. souring machine, -menge, /. amount of acid, -messer, m. acidimeter hydrometer, -messkunst, /. acidimetry. -messtmg, /. acidimetry. -probe, /. acid test acid sample, -pumpe,/. acid pump, -radikal, n. acid radical, -regenerat, n. Rubber) acid reclaim. 

Testing should include a dielectric strength test to confirm the oil s insulation capability and an acidity test, which indicates oil oxidation. While acid formation does not usually develop until the oil has been in service for some time when it does occur the process can be rapid. If acidity is below 0.5 mg KOH/g no action would seem necessary. Between 0.5 and 1 mg KOH/g, increased care and testing is essential. Above 1 the oil should be removed and either reconditioned or discarded. Before the unit is filled with a fresh charge of oil it should be flushed. 

Ratios well below 1 may indicate financial problems ahead while those substantially greater than 1 may point to poor credit control or under-utilization of cash. This ratio is sometimes known as the acid test . The principal profitability ratio in use is the net profit before interest and tax (NPBIT) to net assets or return on capital employed. 

The acid resistance called for on domestic appliances varies with the particular component, e.g. the oven interior of a gas cooker necessitates a higher resistance than the outside sides —the former being at least Class A using 2% sulphuric acid while the latter can have a lower grading based on the less aggressive citric acid tests. These tests are detailed in BS 1344 Part 3 (ISO 8290) and BS 1344 Part 2 (ISO 2722), respectively. 

The evaluation of heat treatments or the effectiveness of stabilisation by limiting carbon content of these stainless steels can be determined by subjecting specimens to the ASTM standardised acid copper sulphate test or boiling nitric acid test (ASTM A262 1986 see also Sections 9.5 and 1.3). 

This test has been developed and used by Streicher as a screening test to be used in conjunction with the tedious boiling nitric acid test for assessing the susceptibility of stainless steels to intergranular attack as specified in ASTM A262 1986, and will be considered subsequently in the section concerned with intergranular attack of Cr-Ni-Fe alloys. 

Nitric acid test t 65 wt.% HNOj Five 48 h exposures to boiling solution refreshed after period Average mass loss per unit area of five testing periods -1- 0-99 to -1- 1-20 1. Chromium-depleted areas 2. <7-phase 3. Chromium carbide... 

Nitric-hydrofluoric acid test 1 10% HNO3 -1- 3% HF 4 h exptosure to 70° C solution Comparison of ratio of mass loss of laboratory annealed and as-received samples of same material Corrosion potential of 304 steel = -l-O-14 to -I-0-54 1. Chromium-depleted areas 2. Not for 0-phase 3. Used only for Mo-bearing steels... 

Hydrochloric acid test 1 10% HCl 24 h in boiling solution 1. Appearance of sample after bending around mandril 2. Mass loss per unit area (a) Redox pxjtential = -I-0-32 (b) Corrosion potential = -0-2 0-1 1. Alloy-depleted area 2. Not for 0-phase... 

It is, however, more likely that the discrepancies observed in the periodate oxidation of malonaldehyde concern mainly the hydroxylation step. In the mechanism proposed (5) for this reaction, it is the enol form of malonaldehyde which is hydroxylated. However, titrations of a solution of malonaldehyde, prepared by hydrolysis of an aqueous solution (33) of carefully distilled 1, 3, 3-tri-ethoxypropene (46, 47), both with strong base and with iodine, indicate that only about 80% of the enol form is present in the equilibrium solution. On the other hand, the thio-barbituric acid test (58, 59) gave consistently higher values for the malonaldehyde content of the solution. The fact that only about 80% of the enol form is present in the equilibrium solution is all the more important as it can be shown (56) by titration with strong base that the enolization is slow, and moreover does not seem to go to completion. 

The aqueous layer should be acidic to litmus paper. If it is basic, indicating that the ammonia was not completely removed from the reaction mixture, more hydrochloric acid should be added until an acidic test is obtained... 

Recovery 93% from amino acid test mixture. b Recovery 100.6% from amino acid test mixture. e Recovery 99.2% from amino acid test mixture. d Decarboxylase-CO method (108, 106). 

The test soln is prepd by dissolving about 5g of Ag nitrate in one liter of distd w. A black coloration is immediately produced on Mg or Mg alloy, the coloration being essentially reduced Ag. No coloration is noted on Al or its alloys, or most other metals. Zn and Cd will show a similar black coloration, but are much heavier (b) Vinegar or acetic acid test Ordinary vinegar or a weak soln of acet ac will give a bubbling reaction in contact with Mg, while other com-... 

When a deposit is tested with concentrated HC1, then made alkaline to precipitate iron, and finally the solution is filtered, the presence of copper is indicated by a clear blue color in the filtrate. Also, if a lightly sanded nail is inserted into the acid test solution, any copper present will plate out on the nail. 

The recovered resin can be reconverted to the hydroxide form by eluting a column of the material with aqueous 10% sodium hydroxide until it is free of halide ion (silver nitrate-nitric acid test) and then with water until the eluent is no longer alkaline to pH paper. 

Brown, DA (2000) The acid test for resting potassium channels. Curr. Biol. 10 R456-R459. Dolphin, AC (1998) Mechanisms of modulation of voltage-dependent calcium channels by G proteins. J. Physiol. 506 3-11. 

In liquid medium, the thiobarbuturic acid test was used to determine polygalacturonase and pectate lyase activity (Sherwood, 1965). 1 ml of the crude enzyme preparation was added to 2 ml of 0.5 N HCl in a test tube. 4 ml of 0.01 M thiobarbuturic acid, dissolved in distilled water, were added. The tubes were heated in a boiling water for Ih and centrifuged. The absorption of the supernatant was determined in the spectrophotometer over the range 480-580 nm. Reaction mixtures without enzyme, which showed no reaction with thiobarbuturic acid, were used as controls. 

Preparation of the alcohol insoluble solids (AIS) The content of the can was drained and the carrot cubes were immediately frozen in hquid nitrogen, freeze-dried and milled. Carrot powder (ca. 10 g) was mixed with 200 ml 80% ethanol previously heated to 60°C. After filtration the residue was extracted with ethanol until the filtrate was colorless (5 times) and gave negative reaction with phenol-sulfuric acid test (Dubois et al., 1956). 

---