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Mercury iodate

Mercury cyanide, 5, 1062 Mercury electrodes potential range aqueous solution, 1, 480 Mercury fluoride, 5. 1059 Mercury fulminate, 2, 7, 12 5, 1063 Mercury halides, 5, 1049 Mercury iodate, 5,1068 Mercury iodide, 5. 1059 Mercury ions Hgf... [Pg.162]

The reaction between micromolar amounts of EDTA and solid mercury iodate is an example of the transportation process based on alternative precipitation. EDTA provides the solubilization of an equivalent amount of iodate and the formation of an Hg(II)-EDTA complex. The filtrate is treated with Ag2S and the EDTA liberated is added to the original sample and brought back into the cycle. [Pg.104]

Iodine occurs to a minute extent (less than 0.001 %) in sea water, but is found in greater concentration, combined in organic form, in certain seaweeds, in oysters and in cod livers. Crude Chile saltpetre, or caliche contains small amounts of sodium iodate, NalOj. from which iodine can be obtained (see below). Some insoluble iodides, for example liiose of silver and mercury(II), occur in Mexico. Iodine is found in the human body in the compound thyroxin in the thyroid gland deficiency of iodine in diet causes enlargement of this gland (goitre). [Pg.319]

Discussion. The mercury is precipitated as mercury(I) chloride and the latter is reacted with standard potassium iodate solution ... [Pg.403]

Procedure. Weigh out accurately about 2.5 g of finely powdered mercury(II) chloride, and dissolve it in 100 mL of water in a graduated flask. Shake well. Transfer 25.0 mL of the solution to a conical flask, add 25 mL water, 2mL 1M hydrochloric acid, and excess of 50 per cent phosphorous(III) acid solution. Stir thoroughly and allow to stand for 12 hours or more. Filter the precipitated mercury(I) chloride through a quantitative filter paper and wash the precipitate moderately with cold water. Transfer the precipitate with the filter paper quantitatively to a 250 mL reagent bottle, add 30 mL concentrated hydrochloric acid, 20 mL water, and 5 mL carbon tetrachloride or chloroform. Titrate the mixture with standard 0.025M potassium iodate in the usual manner (Section 11.127). [Pg.403]

The amount of reddish-purple acid-chloranilate ion liberated is proportional to the chloride ion concentration. Methyl cellosolve (2-methoxyethanol) is added to lower the solubility of mercury(II) chloranilate and to suppress the dissociation of the mercury(II) chloride nitric acid is added (concentration 0.05M) to give the maximum absorption. Measurements are made at 530nm in the visible or 305 nm in the ultraviolet region. Bromide, iodide, iodate, thiocyanate, fluoride, and phosphate interfere, but sulphate, acetate, oxalate, and citrate have little effect at the 25 mg L 1 level. The limit of detection is 0.2 mg L 1 of chloride ion the upper limit is about 120 mg L . Most cations, but not ammonium ion, interfere and must be removed. [Pg.700]

Unexpected uniformities observed in the impact-sensitivities of a group of 22 amminecobalt oxosalts are related to kinetic factors during the initiation process [6], A series of ammine derivatives of cadmium, cobalt, copper, mercury, nickel, platinum and zinc with (mainly) iodate anions was prepared and evaluated as explosives [7], Earlier, ammine and hydrazine derivatives of cadmium, cobalt, copper and nickel with chlorate or perchlorate anions had been evaluated as detonators. Dihydrazinecopper(II) chlorate had exploded when dried at ambient temperature [8],... [Pg.58]

Mercury(I) bromate, 0271 Potassium iodate, 4619 Silver iodate, 0020 Sodium iodate, 4624 Zinc bromate, 0279 See Other METAL OXOHALOGENATES... [Pg.239]

Several explosive salts including the acetylide, azide, borate, bromate, chlorate, chromate, iodate (and ammonium iodate double salt), nitrite, perchlorate (and ammonium perchlorate double salt), periodate, permanganate, picrate and trinitrobenzoate were prepared. The 3 latter salts and the acetylide, azide and bromate are impact-sensitive detonators [1], It appears probable that many of the explosively unstable compounds [2], formed in various ways from interaction of mercury or its compounds with ammonia or its salts, may have the common polymeric structure now recognised for Millon s base [3], This is a silica-like network of N+ and Hg in 4- and 2-coordination, respectively, with OH and water in the interstitial spaces. Individually indexed compounds are Poly(dimercuryimmonium acetylide)... [Pg.342]

Sulphates of the alkali and alkaline earth metals, when heated with sulphur, are converted into sulphide, polysulphide and thiosulphate, with simultaneous formation of sulphur dioxide many other sulphates, e.g. those of copper, mercury, silver and lead, yield only sulphide.7 Other salts of the metals behave in a similar- manner, undergoing transformation into sulphides, the change being effected more readily with the salts of the heavy metals, many of which indeed react slowly with sulphur even at 100° C. in the presence of water.8 At 150° to 200° C. mercuric, stannic and ferric salts in aqueous solution are quantitatively reduced by sulphur mercurous, cupric, bismuth and lead salts arc slowly but quantitatively precipitated as sulphides. Nitrates, permanganates and iodates cause oxidation of the sulphur to sulphuric acid. [Pg.38]

Mercury (II) nitrate White precipitate of mercury (II) iodate... [Pg.532]

Mercury(II) nitrate solution white precipitate of mercury(II) iodate (difference from chlorate and bromate). Lead acetate solution similarly gives a precipitate of lead iodate. Mercury(II) chloride solution, which is practically un-ionized (as mercuric chloride is covalent) gives no precipitate. [Pg.341]

Numerous salts containing oxoanions see Oxoanion), including the nitrate, perchlorate, chlorate, bromate, iodate, and sulfate, are known. Of these, only the nitrate, chlorate, and perchlorate demonstrate a fair degree of water solubility and these serve as a source of insoluble mercury(l) salts through metathesis reactions in water. The nitrate crystallizes as a dUiydrate, Hg2(N03)2-2H20 see Hydrates), which contains linear O-Hg-Hg-0 linkages. The nitrate is stable in acid solution at higher pH it precipitates as Hg(0H)(N03). [Pg.2589]

Explosive reaction with chlorosulfuric acid, hydroiodic acid, magnesium perchlorate, chromyl chloride. Forms sensitive explosive mixtures with metal halogenates (e.g., chlorates, bromates, or iodates of barium, calcium, magnesium, potassium, sodium, zinc), ammonium nitrate, mercury(1) nitrate, silver nitrate, sodium nitrate, potassium permanganate. Violent reaction or ignition with alkalies + heat, fluorine, chlorine, liquid bromine, antimony pentachloride. Reacts with hot alkalies or hydroiodic acid to form... [Pg.1118]


See other pages where Mercury iodate is mentioned: [Pg.333]    [Pg.333]    [Pg.230]    [Pg.259]    [Pg.868]    [Pg.114]    [Pg.119]    [Pg.134]    [Pg.246]    [Pg.309]    [Pg.313]    [Pg.316]    [Pg.317]    [Pg.324]    [Pg.351]    [Pg.352]    [Pg.393]    [Pg.532]    [Pg.598]    [Pg.397]    [Pg.982]    [Pg.1068]    [Pg.979]    [Pg.217]    [Pg.323]    [Pg.458]    [Pg.27]    [Pg.114]    [Pg.119]    [Pg.246]    [Pg.309]   
See also in sourсe #XX -- [ Pg.1068 ]

See also in sourсe #XX -- [ Pg.5 , Pg.1068 ]




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