Lead salts, solubility

Lead(Il) chromate VI) is precipitated when a soluble chromate(VI) or dichromatelVl) is added to a solution of a lead salt in neutral or slightly acid solution ... 

Lead oxide is used in producing fine "crystal glass" and "flint glass" of a high index of refraction for achromatic lenses. The nitrate and the acetate are soluble salts. Lead salts such as lead arsenate have been used as insecticides, but their use in recent years has been practically eliminated in favor of less harmful organic compounds. 

Triiodoacetic acid [594-68-3] (I CCOOH), mol wt 437.74, C2HO2I3, mp 150°C (decomposition), is soluble in water, ethyl alcohol, and ethyl ether. It has been prepared by heating iodic acid and malonic acid in boiling water (63). Solutions of triiodoacetic acid are unstable as evidenced by the formation of iodine. Triiodoacetic acid decomposes when heated above room temperature to give iodine, iodoform, and carbon dioxide. The sodium and lead salts have been prepared. 

The carbonates, sulfates, nitrates, and haUdes of lead (except the yeUow iodide) are colodess. Bivalent lead forms a soluble nitrate, chlorate, and acetate a slightly soluble chloride and an insoluble sulfate, carbonate, chromate, phosphate, molybdate, and sulfide. Highly crystalline basic lead salts of both anhydrous and hydrated types are readily formed. Tetrabasic lead sulfate [52732-72-6] 4PbO PbSO, and the hydrated tribasic salt [12397-06-7] ... 

Lead Sesquioxide. Lead sesquioxide (lead trioxide), Pb202, is an amorphous, orange-yeUow powder soluble ia cold water. It decomposes ia hot water and ia acids to lead salts plus Pb02. Lead sesquioxide can be prepared from lead dioxide by hydrothermal dissociation (43). 

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. 

The anodic behaviour of Pb varies depending upon the electrolyte composition and the electrode potential and has been the subject of a number of reviews . In NO,", CHjCOO and BF4" solutions, lead will form highly soluble lead salts whilst in Cl" and 804 solutions, insoluble lead salts are formed when Pb is anodically polarised. 

Since the early days of using PVC separators in stationary batteries, there has been a discussion about the generation of harmful substances caused by elevated temperatures or other catalytic influences, a release of chloride ions could occur which, oxidized to perchlorate ions, form soluble lead salts resulting in enhanced positive grid corrosion. Since this effect proceeds by self-acceleration, the surrounding conditions such as temperature and the proneness of alloys to corrosion as well as the quality of the PVC have to be taken carefully into account. 

Both solubilities are low, as we would expect for a salt with a small value of. S sp. Notice that PbCl2 is about 350 times less soluble in the NaCl solution. This makes sense in terms of the common-ion effect. The excess chloride ion suppresses the solubility of Pb by Le Chatelier s principle. The actual concentration of lead in seawater is much less than 4.0 X 10 M. This is because other lead salts are much less soluble than lead(II) chloride. The ocean contains carbonate, for example, and. STsp for lead(II) carbonate is quite small, 7.4 X lO ". ... 

The stabilizer or stabilization system used depends on the heat and shear likely to be experienced by the polymer during processing, the end use application requirements, such as clarity or color, and the health concerns. A major health issue has been identified with the lead salts and soaps, because of their relative solubility and their corresponding potential to leach into water. For this reason, lead stabilizers currently find use only when other stabilizer systems do not provide the necessary stabilization or end use properties. Wire and cable sheathing is the only remaining application where the use of the lead stabilizer systems is widespread. Since most humans do not chew on wires (though mice, rats, and squirrels do) and lead-based stabilizers provide superior electrical properties, lead salts persist in this application. 

The sonochemical studies of lead in aqueous solutions are limited due to many insoluble or sparingly soluble lead salts in water, yet few attempts to prepare... 

Soy proteins are used extensively in meat and meat products by the military, the school lunch program and consumers to save money. Their ultimate acceptability is equally dependent upon the nutritional, chemical, sensory and shelf life changes which occur when they are added. Soy proteins in meat products such as ground beef inhibit rancidity, improve tenderness, increase moisture retention, decrease cooking shrink, fat dispersion during cooking and have no important effect on microbiological condition. Concomittantly, inordinate amounts of added soy protein may cause the meat product to be too soft, exhibit an undesirable flavor and may lead to a decreased PER and a deficiency in B-vitamins and trace minerals. In emulsified meat products, soy protein effectively binds water but does not emulsify fat as well as salt soluble muscle protein. Prudent incorporation of plant proteins can result in an improvement of the quality of the meat product with inconsequential adverse effects. 

Note The solution must be prepared and stored in polyethylene or glass containers free from soluble lead salts. 

A different application of visible microscopy was pioneered by Gomori. In 1941 he showed that alkaline phosphatase could be specifically located by its hydrolysis of soluble phosphate esters (initially glycerophosphate). If calcium ions were present in the medium in which the sections were incubated, insoluble calcium phosphate precipitated as a result of the action of the hydrolase. The site of the precipitate could be visualized if cobalt or lead salts were subsequently added to replace calcium and the sections exposed to hydrogen sulfide. In principle many hydrolases and other enzymes could be studied using the appropriate substrates and precipitants. It was important to ensure that the products of the enzyme reactions did not diffuse from the sites where the enzymes were located. It was also essential that the reagents could reach the enzyme site. 

The toxic effects are greater than other lead salts because lead nitrate is more soluble. Moderately toxic by ingestion and other routes of exposure. The compound also is an irritant to eye, skin, and mucous membranes. 

The extremely low solubility of lead phosphate in water (about 6 x 10 15m) again suggests potentiometric analysis. Selig57,59 determined micro amounts of phosphate by precipitation with lead perchlorate in aqueous medium. The sample was buffered at pH 8.25-8.75 and a lead-selective electrode was used to establish the end-point. The detection limit is about 10 pg of phosphorus. Anions which form insoluble lead salts, such as molybdate, tungstate or chromate, interfere with the procedure. Similar direct potentiometric titrations of phosphate by precipitation as insoluble salts of lanthanum(III), copper(II) or cadmium(II) are suggested, the corresponding ion-selective electrodes being used to detect the end-point. 

Extraction efficiency is not the only factor to be examined in the choice of solvent or reagent for a particular application. Environmental, as well as economic considerations must be taken into account. Solvents such as benzene and chloroform (which have solubilities of 0.07 and 0.82 parts per 100 parts of water) might be preferred for extractive efficiency, but their use would result in large losses to the aqueous phase. Not only would this be expensive, but it would be undesirable for reasons of health the toxic organo lead salts would be removed, but an equally toxic organic solvent would be added to the effluent. Addition of a solvent recovery unit subsequent to the extraction step might render the technique uneconomic (relative to alternative effluent treatment techniques). 

Prepare about 30 g. of normal lead chromate, PbCr04 (Exercise 23), by the double decomposition of lead acetate and potassium dichromate and wash the precipitate until it is free from soluble lead salts. Suspend the yellow chromate in a dilute solution of sodium hydroxide (1 20) and boil until the color has changed to a bright brick red. This material is a basic chromate known as chrome red, having the composition represented by the formula PbCr04-PbO ... 

Antidotes.—Two classes of agents axe known, which lessen or destroy the poisonous effects of lead thess are sulphide of hydrogen and the soluble metallic sulphides, snd sulphuric aeid and the soluble sulphates. With the first class, black sulphide of lead is immediately formed, and as this body is almost inert, if not imm cuoue, the further deleterious action of the lead salt is... 

Lead salts similarly yield a precipitate of thiosulphate, soluble in excess of alkali thiosulphate, which also blackens on warming, but the decomposition of the lead thiosulphate is less straightforward, a considerable quantity of sulphur being present in the greyish product.7 Barium chloride with a concentrated solution of an alkali thiosulphate forms a crystalline precipitate of sparingly soluble barium thiosulphate, of which one part dissolves in 480 of water at 18° C.8... 

Cyanamide pigments are produced from industrial-grade calcium cyanamide which is first dissolved. Sulfide and phosphide impurities are precipitated as iron or lead salts [5.127]—[5.132] or oxidized [5.133] [5.135] and filtered off together with graphite impurities. The pure calcium cyanamide is reacted in an aqueous medium with soluble lead or zinc salts or with a slurry of lead oxide or zinc oxide [5.127], [5.129], [5.133], [5.136]—[5.138]. The pigments are filtered, washed, dried, and ground. Zinc cyanamide [5.139] and pure lead cyanamide are not explosive. An explosion reported during the production of lead cyanamide was caused by contamination with small amounts of acid or nitrates [5.140],... 

Arsenate. Lead arsenate. CAS 10031-13-71 nrsenaieoflead Pirn A 04).. while precipitate, formed by reaction of soluble lead salt solution and sodium arsenate solution L scd as an insecticide. Banned or tightly controlled in some countries. 

Carbonates. Lead carbonate PbCOo white precipitate, formed by-reaction of soluble lead sail solution and sodium carbonate solution in ihe cold basic lead carbonate, formed hv reaction nl (II soluble lead salt solution and hoi sodium carbonate solution, and (2i lead sheets, carbon dioxide and aeccic acid, and pigment, the quality depending largely upon the conditions of the reaction. 

Chromates. Lead eliminate, "chrome yellow" PhCrOj. yellow precipitate. by reaction of soluble lead salt solution and sodium dieltromaie or chromate solution, inching point ol lead chromate S44 C. Used as a pigment basic lead chromate, red solid, insoluble, formed by healing lead chromate and sodium hydroxide solution. 

---