Colourants inorganic

A recent survey of the technical and environmental aspects of inorganic pigments by Schwarz and Endriss [33] has put the importance of these products into numerical perspective. Of a total worldwide production of some 5M tonnes of pigments, 96% are inorganic. Of this 4.8M tonnes, carbon black and various whites account for 84%, that is just over 4M tonnes. This means that world production of coloured inorganic pigments is approximately 0.8M tonnes. 

The major use (60%) for coloured inorganic pigments, such as iron oxides, is in the construction materials industry. Here they are used to colour roof and flooring tiles, fibrous cement and mortar. Many inorganic pigments are used in coloured baking enamels for metal appliances. Chromium oxide is used in the refractory industry, not for its colour but because of its ability to improve the properties of bricks used in furnace linings. 

The most important coloured inorganic pigments are iron oxides, which provide shades ranging from yellow and red to brown and black. These pigments are manufactured either from natural deposits or by synthetic routes. However, the S3mthetic products, which offer the advantages over their natural counterparts of higher chemical purity and better... 

We begin our discussion of nanocrystals in diis chapter widi die most challenging problem faced in die field die preparation and characterization of nanocrystals. These systems present challenging problems for inorganic and analytical chemists alike, and die success of any nanocrystal syndiesis plays a major role in die furdier quantitative study of nanocrystal properties. Next, we will address die unique size-dependent optical properties of bodi metal and semiconductor nanocrystals. Indeed, it is die striking size-dependent colours of nanocrystals diat first attracted... 

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). 

If the filtrate has a faint p>ermanganate colour, add a few drops of sodium bisulphite solution until the solution is colourless. In this case (compare o-chlorobenzoic acid) concentration of the solution before precipitation only increases the yield by about 1 g. and may cause occlusion of inorganic salts. 

If an appreciable amount of residue remains, note its colour. Add a few drops of water and test the solution (or suspension) with htmus or with Universal indicator paper. Then add a httle dilute hydrochloric acid and observe whether efiervesceiice occurs and the residue dissolves. Apply a flame test with a platinum wire on the hydrochloric acid solution to determine the metal present. (In rare cases, it may be necessary to subject a solution of the residue to the methods of qualitative inorganic analysis to identify the metal or metals present.) If the flame test indicates sodium, repeat the ignition of the substance on platinum foil. 

Dimethyl-l,10-phenanthrolinedisulfonic acid, di-Na salt (H2O) (bathocuproine-disulfonic acid di-Na salt) [52698-84-7] M 564.5, pKEst 0 (for free acid). Inorganic salts and some coloured species can be removed by dissolving the crude material in the minimum volume of water and precipitating by adding EtOH. Purified reagent can be obtained by careful evapn of the filtrate. 

Frit may be milled dry or wet. The long established dry process is used for cast iron baths and for chemical plant. Vitreous enamel application by a dry electrostatic method is being used on an increasing scale. In these cases, the frit is milled alone, or with inorganic colouring or refractory additives. This is achieved in cylinders using balls of porcelain, steatite or more dense alumina, or with pebbles of flint, to produce a fine powder of predetermined size. 

Phenol-formaldehyde (phenolic) plastics The chemical resistance is affected by the phenol used, cresols giving the best acid resistance whilst xylenols are often used to obtain the best alkali resistance. For chemical-resistant applications the fillers used in moulding powder and reinforcing material in laminates should be inorganic, e.g. asbestos or glass. The resins are usually dark in colour. 

In cases where it proves impossible to find a suitable indicator (and this will occur when dealing with strongly coloured solutions) then titration may be possible by an electrometric method such as conductimetric, potentiometric or amperometric titration see Chapters 13-16. In some instances, spectrophotometric titration (Chapter 17) may be feasible. It should also be noted that ifit is possible to work in a non-aqueous solution rather than in water, then acidic and basic properties may be altered according to the solvent chosen, and titrations which are difficult in aqueous solution may then become easy to perform. This procedure is widely used for the analysis of organic materials but is of very limited application with inorganic substances and is discussed in Sections 10.19-10.21. 

In view of the selective character of many colorimetric reactions, it is important to control the operational procedure so that the colour is specific for the component being determined. This may be achieved by isolating the substance by the ordinary methods of inorganic analysis double precipitation is frequently necessary to avoid errors due to occlusion and co-precipitation. Such methods of chemical separation may be tedious and lengthy and if minute quantities are under consideration, appreciable loss may occur owing to solubility, supersaturation, and peptisation effects. Use may be made of any of the following processes in order to render colour reactions specific and/or to separate the individual substances. 

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