Iodide nitrate

Merkuri-jodid, n. mer curic iodide, mercury (II) iodide, -nitrat, n. mercuric nitrate, mercury-(II) nitrate. -oxyd, n. mercuric oxide, mercury (II) oxide, -rhodanid, n. mercuric thiocyanate, mercury(II) thiocyanate, -salz, n. mercuric salt, mercury (II) salt, -sulfati n. mercuric sulfate, mercury (II) sulfate, -sulfidt ti. mercuric sulfide, mercury (II) sulfide. -sulfozyamd, n. mercuric thiocyanate. 

Merkuro-. mercurous, mercury (I), -azetat, n. mercurous acetate. mercury(I) acetate, -chlorld, n. mercurous chloride, mercury(I) choride. -chrom, n. (Pharm.) mercuro chrome, -jodid, n. n ercurous iodide, mer-cury(I) iodide. -nitrat, n. mercurous nitrate, mercury(I) nitrste. -oxyd, n. mercurous oxide, mercury(I) oxide, -salz, n. mercurous salt, mercury (I) salt, -sulfat, n. mercurouasulfate, mercury(I) sulfate, -sulfid, n. mercurous sulfide, mercury(I) sulfide, -verbindung, /. mercurous compound, mercury (I) compound. 

Stathakis and Cassidy, on his part, used a-, y- (0—40mM/L), or -cyclodextrin (0—lOmM/L) to separate a mix containing iodide, nitrate, perchlorate, thiocyanate, bromate, iodate, ethanesulfonate, pentanesulfonate, and octanesulfonate. The separation of nitrate and nitrite can be improved by the addition of 3% a-cyclodextrin in a 30mM PDC buffer at pH 5.4 (Figure 15). 

In aqueous media lutetium occurs as tripositive Lu3+ ion. All its compounds are in +3 valence state. Aqueous solutions of all its salts are colorless, while in dry form they are white crystalline solids. The soluble salts such as chloride, bromide, iodide, nitrate, sulfate and acetate form hydrates upon crystallization. The oxide, hydroxide, fluoride, carbonate, phosphate, and oxalate of the metal are insoluble in water. The metal dissolves in acids forming the corresponding salts upon evaporation of the solution and crystallization. 

Bromide > chloride > thiocyanate > iodide > nitrate > perchlorate... 

The solubility of potassium chlorate is depressed by the addition of other potassium salts, or by the addition of other chlorates F. Winteler, and T. Schlosing have measured the solubility of potassium chlorate in potassium chloride soln. and of sodium chlorate in soln. of sodium chloride. In accord with the general rule, the solubility is diminished by the addition of a salt with a common ion. S. Arrhenius measured the solubility of potassium chlorate in aq. soln. of potassium nitrate and C. Blarez in aq. soln. of potassium bromide, chloride, iodide, nitrate, sulphate, oxalate, and hydroxide H. T. Calvert, and J. N. Bronsted in an aq. soln. of the last-named compound. H. T. Calvert also measured the solubility of potassium... 

Chloride, bromide, iodide, nitrate, nitrite and thiocyanate... 

Tannic acid Potassium bisulfate, chlorate, cyanide, dichromate, ferricyanide, ferritartrate, iodide, nitrate, oxalate, permanganate... 

Bromate, bromide, chromate, iodate, iodide, nitrate, nitrite, thiocyanate 3-pm SAX or OT-Dionex AS5A particles electrostatically bound to the wall [170]... 

Chlorhexidine salts of low aqueous solubility are formed and may precipitate from chlorhexidine solutions of concentration greater than 0.05% w/v, when in the presence of inorganic acids, certain organic acids, and salts (e.g. benzoates, bicarbonates, borates, carbonates, chlorides, citrates, iodides, nitrates, phosphates, and sulfates). At chlorhexidine concentrations below 0.01% w/v precipitation is less likely to occur. 

In addition to DMAC, the solvents DMF, DMSO and UMP can be used for casting aromatic polyamide membranes. Lyotropic salts that give good polyamide membranes are those with lithium, calcium and magnesium as the cation and chloride, bromide, iodide, nitrate, thiocyanate and perchlorate as the anion. 

An alternative route to the occlusion of salts in zeolite systems is by means of high temperature reactions involving previously imbibed salts. This procedure has been successfully employed to fill the zeolite cages of X, Y and A zeolites with anions such as chloride, bromide, iodide, nitrate and chlorate (refs. 4,7). It offered a possible means of occluding the oxyanions of transition metals such as Cr, Mo and W in the sodalite cages of hydroxy-sodalite and zeolites. 

The construction of these electrodes is shown in Figure 13.12. The most successful example is the fluoride electrode. The membrane consists of a single crystal of lanthanum fluoride doped with some europium(II) to increase the conductivity of the crystal. Lanthanum fluoride is very insoluble, and this electrode exhibits Nerstian response to fluoride down to 10 M and non-Nerstian response down to 10 M (19 ppb ). This electrode has at least a 1000-fold selectivity for fluoride ion over chloride, bromide, iodide, nitrate, sulfate, monohydrogen phosphate, and bicarbonate anions and a 10-fold selectivity over hydroxide ion. Hydroxide ion appears to be the only serious interference. The pH range is limited by the formation of hydrofluoric acid at the acid end and by hydroxide ion response at the alkaline end a pH range of 4 to 9 is claimed... 

Neodymium oxide was first isolated from a mixture of oxides called didymia. The elemeut ueodymium is the secoud most abuudaut lanthanide elemeut in the igneous rocks of Earth s crust. Hydrated neodymium(III) salts are reddish and anhydrous neodymium compounds are blue. The compounds neodymium(III) chloride, bromide, iodide, nitrate, perchlorate, and acetate are very soluble neodymium sulfate is somewhat soluble the fluoride, hydroxide, oxide, carbonate, oxalate, and phosphate compoimds are insoluble. 

Inorganic, Water-soluble Nickel Compounds Nickel is present as Ni " " in common, water-soluble nickel compounds, such as the acetate, bromide, chloride, fluoride, iodide, nitrate, sulfamate, and sulfate salts. Nickel exists in aqueous solutions primarily as the green hexaquonickel ion, Ni(H20)g, which is poorly absorbed by most living organisms. 

Chloride plays an essential role in the ox) en-evolving process. Chloride depletion of PSII samples results in the inactivation of the OEC. Addition of certain anions restores the oxygen evolution activity. The eflFecriveness of the anions follows the order chloride bromide iodide - nitrate. The loss of the two polypeptides, 17 kDa and 23 kDa, induces an increased demand for Cl in order to retain optimal function of the water-oxidizing reaction, suggesting a role for Cl in maintaining the protein organization needed for 02-evolution. ... 

Stepwise anion coordination equilibria are also observed in the Cu(ll) complexes of ligands 113 and 114 [76]. UV/vis titrations in acetonitrile solution show that each Cu(II) complex binds two anions (chloride, bromide, iodide, nitrate or thiocyanate), the first at the Cu(ll) centre and the second in the bis-imidazoHum compartment. The Cu(I) complexes of these ligands are able to host only one nitrate anion (in the bis-imidazolium cavity), while other anions induce demetallation. Cyclic voltammetry and spectroelectro-chemical experiments showed that in the presence of one equivalent of nitrate the Cu(II)/Cu(I) redox change causes the anion to translocate quickly and reversibly from the metal-based binding site in the Cu(II) complex to the im-idazolium binding site in the Cu(I) system. 

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