Acid Hydrochloric Nitric

Aqueous solutions of many salts, of the common strong acids (hydrochloric, nitric and sulphuric), and of bases such as sodium hydroxide and potassium hydroxide are good conductors of electricity, whereas pure water shows only a very poor conducting capability. The above solutes are therefore termed electrolytes. On the other hand, certain solutes, for example ethane-1,2-diol (ethylene glycol) which is used as antifreeze , produce solutions which show a conducting capability only little different from that of water such solutes are referred to as non-electrolytes. Most reactions of analytical importance occurring in aqueous solution involve electrolytes, and it is necessary to consider the nature of such solutions. 

Inorganic and organic acids (hydrochloric, nitric, sulfuric, and trichloroacetic) and bases (hot caustic soda)... 

Corrosives damage by chemical destruction of the tissue they contact. Strong acids (hydrochloric, nitric and sulfuric) or alkalis (sodium hydroxide and potassium hydroxide) can cause corrosive bums. Alkalis can cause progressive bums, meaning the injury increases as the alkali moves through the damaged tissue. This is especially critical in injuries to the eye, where delicate tissues can be damaged little by little until vision is destroyed. The severity of a corrosive bum depends on ... 

Tin slowly dissolves in dilute hydrochloric, nitric and sulphuric acids, and is in fact the only Group IV element to do so. The reactions with more concentrated acid are rapid. With hydrochloric acid. 

Acids such as sulfuric, hydrochloric, nitric, and especially hydrofluoric as well as strong alkaUes such as caustic soda and caustic potash are extremely corrosive to animal and vegetable tissue. Extreme caution must be taken to prevent skin contact, inhalation, or ingestion. Violent reactions may occur when dissolving or diluting many of these chemicals with water. 

Acid Treatment. The treatment of petroleum products with acids has been in use for a considerable time in the petroleum industry. Various acids such as hydrofluoric acid, hydrochloric acid, nitric acid, and phosphoric acid have been used in addition to the most commonly used sulfuric acid, but in most instances there is Httie advantage in using any acid other than sulfuric. 

In the tributyl phosphate extraction process developed at the Ames Laboratory, Iowa State University (46—48), a solution of tributyl phosphate (TBP) in heptane is used to extract zirconium preferentially from an acid solution (mixed hydrochloric—nitric or nitric acid) of zirconium and hafnium (45). Most other impurity elements remain with the hafnium in the aqueous acid layer. Zirconium recovered from the organic phase can be precipitated by neutralization without need for further purification. 

Precipitated or synthetic barium carbonate is the most commercially important of all the barium chemicals except for barite. Barium carbonate is an unusually dense material, that is almost kisoluble ki water and only slightly soluble ki carbonated water. It does dissolve ki dilute hydrochloric, nitric, and acetic acids and is also soluble ki ammonium nitrate and ammonium chloride solutions. 

BeryUium reacts readUy with sulfuric, hydrochloric, and hydrofluoric acids. DUute nitric acid attacks the metal slowly, whereas concentrated nitric acid has Httle effect. Hot concentrated alkaUes give hydrogen and the amphoteric beryUium hydroxide [13327-32-7] Be(OH)2. Unlike the aluminates, the beryUates are hydrolyzed at the boU. 

MetaUic impurities in beryUium metal were formerly determined by d-c arc emission spectrography, foUowing dissolution of the sample in sulfuric acid and calcination to the oxide (16) and this technique is stUl used to determine less common trace elements in nuclear-grade beryUium. However, the common metallic impurities are more conveniently and accurately determined by d-c plasma emission spectrometry, foUowing dissolution of the sample in a hydrochloric—nitric—hydrofluoric acid mixture. Thermal neutron activation analysis has been used to complement d-c plasma and d-c arc emission spectrometry in the analysis of nuclear-grade beryUium. 

The cmde product containing aminotria ines can be purified by digestion with acids (eg, hydrochloric, nitric, or sulfuric) this hydroly2es the acycHc impurities to carbon dioxide and ammonia and the aminotria ines to CA and ammonia. 

Inorga.nicNIa.teria.ls. These include acids (sulfuric, nitric, hydrochloric, and phosphoric), bases (caustic soda, caustic potash, soda ash, sodium carbonate, ammonia, and lime), salts (sodium chloride, sodium nitrite, and sodium sulfide) and other substances such as chlorine, bromine, phosphoms chlorides, and sulfur chlorides. The important point is that there is a significant usage of at least one inorganic material in all processes, and the overall toimage used by, and therefore the cost to, the dye industry is high. 

Mineral acid Hydrobromic acid Hydrochloric acid Hydrofluoric acid Nitric acid Sulphuric acid... 

Perchloric acid Sulfuric acid Hydrochloric acid Nitric acid... 

The furnace scales which form on alloy steels are thin, adherent, complex in composition, and more difficult to remove than scale from non-alloy steels. Several mixed acid pickles have been recommended for stainless steel, the type of pickle depending on the composition and thickness of the scale For lightly-scaled stainless steel, a nitric/hydrofluoric acid mixture is suitable, the ratio of the acids being varied to suit the type of scale. An increase in the ratio of hydrofluoric acid to nitric acid increases the whitening effect, but also increases the metal loss. Strict chemical control of this mixture is necessary, since it tends to pit the steel when the acid is nearing exhaustion. For heavy scale, two separate pickles are often used. The first conditions the scale and the second removes it. For example, a sulphuric/hydrochloric mixture is recommended as a scale conditioner on heavily scaled chromium steels, and a nitric/hydrochloric mixture for scale removal. A ferric sulphate/ hydrofluoric acid mixture has advantages over a nitric/hydrofluoric acid mixture in that the loss of metal is reduced and the pickling time is shorter, but strict chemical control of the bath is necessary. 

The most commonly used chromate passivation process is the Cronak process developed by the New Jersey Zinc Co. in 1936, in which the parts are immersed for 5-10 s in a solution containing 182 g/1 sodium dichromate and 6ml/l sulphuric acid. A golden irridescent film is formed on the zinc or cadmium surface. Many variants (all fairly acidic) have been developed subsequently all are based on dichromate (or chromic acid) with one or more of the following sulphuric acid, hydrochloric acid (or sodium chloride), nitric acid (or nitrate), phosphoric acid, formic acid and acetic acid. A survey by Biestek shows that several of these variants are as good as the Cronak process, although none is superior. 

The cobalt complex is usually formed in a hot acetate-acetic acid medium. After the formation of the cobalt colour, hydrochloric acid or nitric acid is added to decompose the complexes of most of the other heavy metals present. Iron, copper, cerium(IV), chromium(III and VI), nickel, vanadyl vanadium, and copper interfere when present in appreciable quantities. Excess of the reagent minimises the interference of iron(II) iron(III) can be removed by diethyl ether extraction from a hydrochloric acid solution. Most of the interferences can be eliminated by treatment with potassium bromate, followed by the addition of an alkali fluoride. Cobalt may also be isolated by dithizone extraction from a basic medium after copper has been removed (if necessary) from acidic solution. An alumina column may also be used to adsorb the cobalt nitroso-R-chelate anion in the presence of perchloric acid, the other elements are eluted with warm 1M nitric acid, and finally the cobalt complex with 1M sulphuric acid, and the absorbance measured at 500 nm. 

D.9 (a) hydrochloric acid (b) sulfuric acid (c) nitric acid ... 

Name Nitric acidPerchloric acidSulfuric acid Hydrochloric acidHydrobromic acidHydriodic acid Structure... 

Am(V), Am02, undergoes disproportionation and redox reactions in aqueous acidic media, which can be followed by spectrophotometry at wavelengths of 812 m/ii for Am(III), 715 m t for Am(V) and 992 mpt for Am(VI). The earlier work " on solutions of Am(V) in hydrochloric, nitric , sulphuric , and perchloric acid media, which were hindered by a-radiation reactions ( Am), led to the conclusion that the rate law... 

In the presence of potassium chlorate/nitric acid/hydrochloric acid mixture, ruthenium oxidises expiosively. Ruthenium is chemically inert like any noble metal and maybe more than any other metal. Indeed, it is inactive vis- -vis aqua regia , but on this occasion potassium chlorate was combined with aqua regia. 

Formic acid, 100-8° Hydrofluoric acid, 19-4° Hydrochloric acid, — 84-0° Hydrobromic acid, — 73° Hydriodic acid, — 35° Nitric acid, 86-0°... 

---