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Nickel nitrate is the inorganic compound Ni(NO 3) 2 or any hydrate thereof. In the hexahydrate, the nitrate anions are not bonded to nickel. Other hydrates have also been reported: Ni(NO 3) 2. 9H 2 O, Ni(NO 3) 2. 4H 2 O, and Ni(NO 3) 2. 2H 2 O. [3] It is prepared by the reaction of nickel oxide with nitric acid: NiO + 2 HNO 3 + 5 H 2 O → Ni ...
n.o.s. = not otherwise specified meaning a collective entry to which substances, mixtures, solutions or articles may be assigned if a) they are not mentioned by name in 3.2 Dangerous Goods List AND b) they exhibit chemical, physical and/or dangerous properties corresponding to the Class, classification code, packing group and the name and description of the n.o.s. entry [4]
The heptahydrate crystallises from water below 31.5 above this blue hexhydrate forms, and above 53.3 the green form. [20] Heating nickel sulfate dehydrates it, and then 700° it loses sulfur trioxide, sulfur dioxide and oxygen. Other important nickel compounds in this class are nickel carbonate, nickel nitrate, and nickel phosphate
The geometry of the nickel(II) ion is square planar. [2] It is surrounded by two equivalents of the conjugate base (dmgH −) of dimethylglyoxime (dmgH 2). The pair of organic ligands are joined through hydrogen bonds to give a macrocyclic ligand.
Nickel nitrate commonly crystallises with six water molecules, [1] but can also be anhydrous, or with two, four or nine waters. [11] triphenylphosphine oxide nickel nitrate [(C 6 H 6) 3 PO] 2 Ni(NO 3) 2 is non ionic, with nitrato as a ligand. It can be made from nickel perchlorate. It is yellow and melts at 266 °C. [12]
Nickel electroplating was developed in the first half of the 19th century, with notable experiments made by Golding Bird (1837) and nickel nitrate patent by Joseph Shore (1840). The first practical recipe, an aqueous solution of nickel and ammonium sulfates, was invented by Böttger in 1843 and was in use for 70 years. [ 8 ]
Nickel hydrazine nitrate (NHN), (chemical formula: [Ni(N 2 H 4) 3](NO 3) 2 is an energetic material having explosive properties in between that of primary explosive and a secondary explosive. [2] It is a salt of a coordination compound of nickel with a reaction equation of 3N 2 H 4 ·H 2 O + Ni(NO 3) 2 →〔Ni(N 2 H 4) 3 〕(NO 3) 2 + 3H 2 O [3]
The blue isomer is prepared by treating hydrated nickel chloride with triphenylphosphine in alcohols or glacial acetic acid: [1] NiCl 2 •6H 2 O + 2 PPh 3 → NiCl 2 (PPh 3) 2 + 6 H 2 O. When allowed to crystallise from chlorinated solvents, the tetrahedral isomer converts to the square planar isomer. The square planar form is red and