Lead acetate preparation

Cotton wool impregnated with lead acetate. Preparation as in p. 8.2.3. 

Prepare a solution of sodium plumbite by adding 10 per cent, sodium hydroxide solution to a few drops of about N lead acetate solution until the white precipitate of lead hydroxide initially formed just redissolves to a clear solution. Add 1 ml. of the fusion solution the presence of sulphiu- is indicated by a black precipitate of lead sulphide. 

PbF2 is readily prepared by the action of hydrogen fluoride on lead hydroxide, lead carbonate, or a-lead oxide. It can also be obtained by precipitation from lead nitrate or lead acetate solutions using potassium fluoride, ammonium fluoride, or ammonium bifluoride. 

Lead Chloride. Lead dichloride, PbCl2, forms white, orthorhombic needles some physical properties are given in Table 1. Lead chloride is slightly soluble in dilute hydrochloric acid and ammonia and insoluble in alcohol. It is prepared by the reaction of lead monoxide or basic lead carbonate with hydrochloric acid, or by treating a solution of lead acetate with hydrochloric acid and allowing the precipitate to settle. It easily forms basic chlorides, such as PbCl Pb(OH)2 [15887-88 ] which is known as Pattinson s lead white, an artist s pigment. 

Lead Carbonate. Lead carbonate [598-63-0] PbCO, mol wt 267.22, d = 6.6g/cm, forms colorless orthorhombic crystals it decomposes at about 315°C. It is nearly insoluble in cold water (0.00011 g/100 mL at 20°C), but is transformed in hot water to the basic carbonate, 2PbC03 Pb(OH)2. Lead carbonate is soluble in acids and alkalies, but insoluble in alcohol and ammonia. It is prepared by passing CO2 iuto a cold dilute solution of lead acetate, or by shaking a suspension of a lead salt less soluble than the carbonate with ammonium carbonate at a low temperature to avoid formation of basic lead carbonate. 

Lead chromates are prepared by precipitation techniques from soluble salts ia aqueous media. The raw material Hst iacludes a number of different lead compounds, eg, Htharge, lead nitrate, basic lead acetate, basic lead carbonate, as well as acids, alkahes, sodium bichromate, and sodium chromate. The typical reaction can be represented by the foUowiag equation ... 

PZN-PT, and YBa2Cug02 g. For the preparation of PZT thin films, the most frequently used precursors have been lead acetate and 2irconium and titanium alkoxides, especially the propoxides. Short-chain alcohols, such as methanol and propanol, have been used most often as solvents, although there have been several successful investigations of the preparation of PZT films from the methoxyethanol solvent system. The use of acetic acid as a solvent and chemical modifier has also been reported. Whereas PZT thin films with exceUent ferroelectric properties have been prepared by sol-gel deposition, there has been relatively Httle effort directed toward understanding solution chemistry effects on thin-film properties. 

Permanent coloration can also be achieved by exposing hair to certain metals copper, silver, and especially lead salts. Preparations containing aqueous solutions of lead acetate may include a source of sulfur, usually thiosulfate, which may react with cystine in the hair to produce some cysteine or may react directiy with the metal ion to form dark metallic sulfides. Preparations of this type, which darken hair gradually, are not universally considered safe. 

Several improved methods for the preparation of known unsaturated azlactones as well as some interesting new compounds of this type have been reported. Crawford and Little observed that the direct use of 2-phenyl-5-oxazolone (1) in the Erlenmeyer reaction gave much improved yields (35-74%) of unsaturated azlactones with aliphatic aldehydes and with ketones such as acetone and cyclohexanone [Eq, (1)], The usual procedure of mixing a carbonyl compound, hippuric acid, acetic anhydride, and sodium (or lead) acetate affords poor yields in the aliphatic series. 

Lauraldehyde, 46, 36 Lead acetate in preparation of selective palladium catalyst, 46, 90... 

Moore MR, Meredith PA, Watson WS, et al. 1980. The percutaneous absorption of lead-203 in humans from cosmetic preparations containing lead acetate, as assessed by whole-body counting and other techniques. Food Cosmet Toxicol 18 399-405. 

The compound (formulated as the double salt, (fuel + oxidant), rather than the mixed salt) may be formed during the preparation of lead bromate from lead acetate and... 

The lead salt decomposes with explosive violence at 150-160°C and should not be dried by heating. The salt prepared from lead acetate explodes more violently than that from the nitrate. 

Testing for Sulphur.—The qualitative test for sulphur is carried out in the same way as that for nitrogen. Ignite the substance in a small tube with sodium, dissolve the product in water, and add to one half of the cooled solution a few drops of sodium nitroprusside solution freshly prepared by shaking a few particles of the solid salt with cold water. A violet colour indicates the presence of sulphur. Since the nitroprusside reaction is extremely sensitive and does not allow any estimate of the amount of sulphur to be made, filter the second half of the liquid, add lead acetate solution to the filtrate, and acidify with acetic acid. According as the amount of sulphur is small or large, a dark turbidity or a more or less heavy precipitate will form. 

Materials Required Arsenic limit test apparatus HgCl2—paper smooth white filter paper (having thickness in mm of 400 paper = weight in g per Sq. M.), soaked in a saturated solution of HgCl2, pressed to get rid of excess of soln. and dried at about 60°C in the dark lead acetate solution 10.0% w/v soln. of PbAc2 in C02 free water KI (AsT), 1.0 g Zn (AsT) 10.0 g Dilute Arsenic solution (AST) Standard stains, Test Solutions—are prepared according to the Indian Pharmacopoeia 1996. 

In analysing the caffeine of energy drinks, an accurately weighed amount of 15 mL of sample to 50 mL volumetric flask containing 25 mL water. Two milliliters of basic lead acetate solution was added to this solution and diluted the mark with distilled water. After filtering, 25 mL of filtrate was taken and 0.25 g of NaHCOj was added to this solution. Then, the solution was filtered. Five milliliters of filtrate was transferred to a 25 mL volumetric flask and adjusted to volume with distilled water. The peak amplitudes of the first-derivative spectra was measured at 287 and 260 nm. The sample preparation procedure was also used for PLS-1 method and the absorbances of this solution were recorded between 240-320 mn. 

Palladium catalysts are more often modified for special selectivities than platinum catalysts. Palladium prepared by reduction of palladium chloride with sodium borohydride Procedure 4, p. 205) is suitable for the reduction of unsaturated aldehydes to saturated aldehydes [i7]. Palladimn on barium sulfate deactivated with sulfur compounds, most frequently the so-called quinoline-5 obtained by boiling quinoline with sulfur [34], is suitable for the Rosenmund reduction [i5] (p. 144). Palladium on calcium carbonate deactivated by lead acetate Lindlar s catalyst) is used for partial hydrogenation of acetylenes to cw-alkenes [36] (p. 44). 

Lead acetate is prepared by dissolving lead monoxide in strong acetic acid ... 

Basic lead acetates are prepared by dissolving lead monoxide in hot dilute acetic acid, or by dissolving the oxide in dilute acetic acid at alkaline pH. They may be made by dissolving lead monoxide in a solution of lead acetate. Crystalline products are obtained upon cooling the solutions. 

Lead carbonate is prepared by passing carbon dioxide into a cold dilute solution of lead acetate ... 

Lead chromate is found naturally in minerals crocoite and phoenicochroite. It also is readily prepared by adding a soluble chromate such as sodium or potassium chromate to a solution of lead nitrate, lead acetate or other soluble lead(II) salt in neutral or slightly acidic solution ... 

Lead diiodide is prepared by mixing aqueous solutions of lead nitrate or lead acetate with an aqueous solution of potassium or sodium iodide or hydri-odic acid, followed hy crystallization. The product is purified hy recrystalliza-tion. 

Lead sulfide occurs naturally as the mineral galena. It can be prepared in the laboratory as a black precipitate by passing hydrogen sulfide through a dilute acid solution of inorganic lead salt, such as lead nitrate or lead acetate ... 

Lead tetraacetate is prepared by dissolving lead tetroxide in warm glacial acetic acid followed by cooling. On cooling, the tetraacetate crystallizes out while lead acetate remains in the solution ... 

Lead azide [Pb(N3)2] (LA) is a salt of hydrazoic acid (N3H, highly poisonous) and is prepared by reacting solutions of sodium azide and lead acetate or nitrate. This exists in two forms the a form (orthorhombic and stable) and P form (monoclinic) which has a tendency to revert back to the a form. The P form is much more sensitive. The two forms differ in their rate of decomposition when heated. Crystalline LA is stored in dry conditions because it becomes more sensitive when... 

Service lead azide (SLA) SLA is prepared by double decomposition of lead acetate and sodium azide in the presence of sodium carbonate and acetic acid. 

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