Nitrite, small amounts

This solution may also be employed in the test for bromine. If iodine has been found, add small amounts of sodium nitrite solution, warm shghtly and shake with fresh 1 ml. portions of carbon tetrachloride until the last extract is colourless boil the acid solution until no more nitrous fumes are evolved and cool. If iodine is absent, use 1 ml. of the fusion solution which has been strongly acidified with glacial acetic acid. Add a small amount of lead dioxide, place a strip of fluorescein paper across the mouth of the tube, and warm the solution. If bromine is present, it will colour the test paper rose-pink (eosin). 

Quality of Product. Ammonium nitrate, commonly made from pure synthetic raw materials, is itself of high purity. If the product is intended for use in explosives, it should be at least 99% ammonium nitrate and contain no more than 0.15% water. It should contain only small amounts of water-insoluble and ether-soluble material, sulfates and chlorides, and should not contain nitrites. The soHd product ought to be free from alkalinity, but be only slightly acidic. 

The nitrites aie most conveniently prepared from the corresponding alcohols by treatment with nitrosyl chloride in pyridine. The crude nitrites can be precipitated by addition of water and recrystallized from appropriate solvents. However nitrites prepared from carbinols in which the adjacent carbon is substituted by halogen, free or esterified hydroxyl or a carbonyl function are very readily hydrolyzed and must be recrystallized with great care. In general the photolysis gives higher yields if purified and dried nitrites are used which do not contain acids or pyridine, although occasionally the addition of small amounts of pyridine is recommended in order to prevent hydrolysis of the nitrite. Traces of acids do in fact catalyze the thermal decomposition of secondary nitrites to equimolar amounts of alcohol and ketone. ... 

Hot aqueous solutions of ammonium nitrite also decompose to give nitrogen though small amounts of NO and HNO3 are also formed (p. 434) and must be removed by suitable absorbents such as dichromate in aqueous sulfuric acid ... 

The reactivity of the 5-position of 2-aminothiophene in diazo coupling, which is present also in the acylated derivatives, complicates the formation of a diazonium salt from 2-aminothiophene. Thus Steinkopf and Miiller obtained only an azo dyestuff, although they proved, through the isolation of small amounts of 2-thienyl diazonium chloride, the diazotizability of 2-aminothiophene which had earlier been denied. However, recent Russian work claims the preparation of 2-thienyldiazonium chloride by treating the double salt in 10% hydrochloric acid with sodium nitrite. Amazingly high yields (over 90%) of azo compounds were then achieved by coupling the diazonium salt solution with y9-naphtol, w-toluidine or with the 2-aminothiophene double salt. These authors have also studied the... 

It is not usual for unopened drums of nitrite-based chemical to degrade, and the product should remain in good condition for several years. However, it is possible for tannin-based corrosion inhibitors to degrade, even in unopened drums. Under warm conditions (such as storage in a boil-erhouse) and in the absence of a small amount of suitable microbiocide in the formulation, plastic drums containing tannin products may swell considerably because of microbiological degradation and gas formation. Care is needed to avoid accidents. 

In this context two observations reported by Rondestvedt (1960, p. 214) should be mentioned (i) Meerwein reactions proceed faster in the presence of small amounts of nitrite ion. Meerwein reactions in which N2 evolution ceased before completion of the reaction can be reinitiated by addition of some NaN02. (ii) Optimal acidity for Meerwein reactions is usually between pH 3 and 4, but lower (pH — 1) with very active diazonium compounds such as the 4-nitrobenzenediazonium ion or the diphenyl-4,4 -bisdiazonium ion. At higher acidities more chloro-de-diazoniation products are formed (Sandmeyer reaction) and in less acidic solutions (pH 6) more diazo tars are formed. 

If an aliphatic amino group is to a COOR, CN, CHO, COR, and so on, and has an a hydrogen, treatment with nitrous acid gives not a diazonium salt, but a diazo compound Such diazo compounds can also be prepared, often more conveniently, by treatment of the substrate with isoamyl nitrite and a small amount of acid. Certain heterocyclic amines also give diazo compounds rather than diazonium salts. ... 

In recent years greater attention has been given to nitrogen containing pesticides and the possibility of their nitrosation in soil. The N-nitrosamines that form may arise from the parent pesticide or from a pesticide metabolite. The reaction calls for favourable pH conditions (pH 3-4) and excess nitrite. Under field conditions, the nitrosable residues are usually present in traces and only small quantities of these will actually be nitrosated in soils. However, the possibility exists that the small amounts of N-nitrosamines could be assimilated by plants. 

In a variation of this procedure [19], a small amount of acid is added to a suspension of a sulphonated amine in sodium nitrite solution the sulphonic acid group on the amine generates nitrous acid and diazotisation proceeds to completion. 

Several members of this (often endothermic) group of compounds which contain heavy metals tend to explosive instability, and most are capable of violent oxidation under appropriate circumstances. Fusion of mixtures of metal cyanides with metal chlorates, perchlorates, nitrates or nitrites causes a violent explosion [1], Addition of one solid component (even as a residue in small amount) to another molten component is also highly dangerous [2], Individually indexed compounds are ... 

Biodegradation of fuel oils in sediments is inhibited under anaerobic conditions (Bartha and Atlas 1977). Under anaerobic conditions, some soil microorganisms are capable of nitrate reduction using fuel oils as the carbon source, although nitrite may be an unwanted by-product. However, the addition of a small amount of oxygen (0.2 volume percent oxygen) to the medium can accelerate the degradation of the oil without the concomitant production of nitrite (Riss and Schweisfurth 1987). 

On Ba/y-AhOj, the NO adsorption proceeded as illustrated in Figure 13.12a, with small quantities of NO species adsorbed on the catalyst surface. The FT-IR spectra [inset (b) in Figure 13.12] showed the progressive formation of nitrite species (band at 1220cm ) up to a 10min exposure time, along vdth small amounts of nitrate... 

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