Nitrated paper Nitrates

The blackening of filter paper, moistened with a soluble lead(II) salt (e.g. the ethanoate or nitrate), by the formation of lead(II) sulphide. 

Filling and sealing the Carius tube. Introduce 100-150 mg. of powdered silver nitrate into the Carius tube, either through a spill of filter -paper rolled and inserted as described on p.418, or through a small funnel, so that the powder falls freely to the bottom of the tube and does not touch or adhere to the walls. 

Method 1. From ammonium chloroplatinate. Place 3 0 g. of ammonium chloroplatinate and 30 g. of A.R. sodium nitrate (1) in Pyrex beaker or porcelain casserole and heat gently at first until the rapid evolution of gas slackens, and then more strongly until a temperature of about 300° is reached. This operation occupies about 15 minutes, and there is no spattering. Maintain the fluid mass at 500-530° for 30 minutes, and allow the mixture to cool. Treat the sohd mass with 50 ml. of water. The brown precipitate of platinum oxide (PtOj.HjO) settles to the bottom. Wash it once or twice by decantation, filter througha hardened filter paper on a Gooch crucible, and wash on the filter until practically free from nitrates. Stop the washing process immediately the precipitate tends to become colloidal (2) traces of sodium nitrate do not affect the efficiency of the catalyst. Dry the oxide in a desiccator, and weigh out portions of the dried material as required. 

Must of the ammonia is evolved in about I hour. The vapour should be tested periodically for the presence of ammonia with mercurous nitrate paper. If traces are still present after 3-4 hours, the solution should be steam distilled for 30 minutes. 

Cautiously add 250 g. (136 ml.) of concentrated sulphuric acid in a thin stream and with stirring to 400 ml. of water contained in a 1 litre bolt-head or three-necked flask, and then dissolve 150 g. of sodium nitrate in the diluted acid. Cool in a bath of ice or iced water. Melt 94 g. of phenol with 20 ml. of water, and add this from a separatory funnel to the stirred mixture in the flask at such a rate that the temperature does not rise above 20°. Continue the stirring for a further 2 hours after all the phenol has been added. Pour oflF the mother liquid from the resinous mixture of nitro compounds. Melt the residue with 500 ml. of water, shake and allow the contents of the flask to settle. Pour oflF the wash liquor and repeat the washing at least two or three times to ensure the complete removal of any residual acid. Steam distil the mixture (Fig. II, 40, 1 or Fig. II, 41, 1) until no more o-nitrophenol passes over if the latter tends to solidify in the condenser, turn oflF the cooling water temporarily. Collect the distillate in cold water, filter at the pump, and drain thoroughly. Dry upon filter paper in the air. The yield of o-nitrophenol, m.p. 46° (1), is 50 g. 

Primary aromatic amides are crystaUine sohds with definite melting points. Upon boiling with 10-20 per cent, sodium or potassium hydroxide solution, they are hydrolysed with the evolution of ammonia (vapour turns red htmus paper blue and mercurous nitrate paper black) and the formation of the alkah metal salt of the acid ... 

It has been necessary to comment upon these various studies because Olah and his co-workers have suggested that whilst nitrations, like those with nitronium salts, which give a relative rate of reaction of toluene with respect to benzene not much greater than unity involve the nitronium ion as the electrophile, this is not so in other cases. It is important to consider these opinions closely. In the earlier of the two relevant papers it is agreed that since nitrations of toluene with nitronium tetrafluoroborate in sulpholan show no abnormal o -ratio there... 

In a later paper Knowles and Norman compared more fully nitrations of benzylic compounds in acetyl nitrate and in mixed acid (table 5.9), and interpreted the results in terms of three factors nitronium ion nitration in both media some degree of protonation of the oxygen... 

It is the purpose of this and the following chapter to report the quantitative data concerning the relationship of structure to orientation and reactivity in aromatic nitration. Where data obtained by modern analytical methods are available they are usually quoted in preference to the results of older work. Many of the papers containing the latter are, however, noted in the brief discussion which is given of interpretations of the results. 

The first three of a series of papers by Ridd and co-workers on Inductive and Field effects in Aromatic Substitution have appeared. Results of studies of the nitration of 4-phenylp5nidine and of 4-benzylpyridine in aqueous sulphuric acid were reported and use of the usual criteria (para 8.2) showed that in each case the conjugate acid was the species undergoing nitration. The values of where fm refers to the corresponding homocyclic compound (biphenyl or diphenylmethane) when plotted against r, the distance between the... 

So what can be done about the mercuric nitrate problem The authors in the original paper from which this recipe came from, clearly call for an amount of mercuric nitrate that is exactly equal... 

O. Skauh, "Pan Granulation of Ammonium Nitrate and Urea," paper presented at the 168th National Meeting of the Mmerican Chemical Society, Adantic City, N.J., 1974. 

MiscelUneous. Mahc acid is used in pharmaceuticals (qv), cosmetics (qv), dentifrices (qv), metal cleaning, electroless plating (46), wash-and-wear textile finishing (47—49), for stabilization of heat-sensitive copying paper (50), as an inhibitor of gelation, livering, and agglomeration in cellulose nitrate Hqueurs, and in many other appHcations. 

G. E. Ericksen, Geology and Origin of the Chilean Nitrate Deposits, U.S. Geological Survey, Professional Paper 1188, U.S. Government Printing Office, Washington, D.C., 1981, 37 pp. 

The principal chemical iadustry based on wood is pulp and paper. In 1995, 114.5 x 10 metric tons of wood were converted iato - 60 x 10 metric tons of fiber products ranging from newsptint to pure cellulose ia the United States (1,76). Pure cellulose is the raw material for a number of products, eg, rayon, cellulose acetate film base, cellulose nitrate explosives, cellophane, celluloid, carboxymethylceUulose, and chemically modified ceUulosic material. 

Sulfide content is determined by titration with standard lead nitrate solution (1 g/L). The titration is continued until a drop of the test solution on a filter paper ceases to produce a stain with a drop of lead nitrate solution. 

Acetone and ammonia are condensed in the presence of various promoters. A 45 per cent yield of diacetonamine isolated as the hydrogen oxalate is claimed when acetone saturated with ammonia at o" is allowed to stand twenty-four hours with 8.5 per cent of ammonium nitrate. Suzuki and Horie, Bull. Inst. Phys.-Chem. Research (Tokyo) ii, 383 (1932). Abstract 30 (in English) published with Sci. Papers Inst. Phys.-Chem. Research (Tokyo) 18, Nos. 350-4 [C. A. 26, 4302 (1932)]. 

Ruthenium (IV) oxide [12036-10-1] M 133.1, d 6.97. Freed from nitrates by boiling in distilled water and filtering. A more complete purification is based on fusion in a KOH-KNO3 mix to form the soluble ruthenate and perruthenate salts. The melt is dissolved in water, and filtered, then acetone is added to reduce the ruthenates to the insoluble hydrate oxide which, after making a slurry with paper pulp, is filtered and ignited in air to form the anhydrous oxide [Campbell, Ortner and Anderson Anal Chem 33 58 1961]. 

Acetylene, fulminic acid (produced in ethanol - nitric acid mixtures), ammonia Acetic acid, acetone, alcohol, aniline, chromic acid, hydrocyanic acid, hydrogen sulphide, flammable liquids, flammable gases, or nitratable substances, paper, cardboard or rags Inorganic bases, amines Silver, mercury... 

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