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Names | |||
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IUPAC name Nickel(II) sulfate | |||
Other names Nickelous sulfate Nickel (II) sulphate | |||
Identifiers | |||
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3D model (JSmol) | |||
ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.029.186 | ||
EC Number |
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PubChem CID | |||
RTECS number |
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UNII |
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CompTox Dashboard (EPA) | |||
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Properties | |||
NiSO4 | |||
Molar mass | 154.75 g/mol (anhydrous) 262.85 g/mol (hexahydrate) 280.86 g/mol (heptahydrate) | ||
Appearance | yellow solid (anhydrous) blue crystals (hexahydrate) green-blue crystals (heptahydrate) | ||
Odor | odorless | ||
Density | 4.01 g/cm3 (anhydrous) 2.07 g/cm3 (hexahydrate) 1.948 g/cm3 (heptahydrate) | ||
Melting point | 1210 °C (anhydrous, at high pressure) 53 °C (hexahydrate) | ||
Boiling point | > 640 °C (anhydrous, decomposes) 100 °C (hexahydrate, decomposes) | ||
65 g/100 mL (20 °C) 77.5 g/100 mL (30 °C) (heptahydrate) | |||
Solubility | anhydrous insoluble in ethanol, ether, acetone hexahydrate insoluble in ethanol, ammonia heptahydrate soluble in alcohol | ||
Acidity (pKa) | 4.5 (hexahydrate) | ||
+4005.0·10−6 cm3/mol | |||
Refractive index (nD) | 1.511 (hexahydrate) 1.467 (heptahydrate) | ||
Structure | |||
orthorombic (anhydrous) tetragonal (hexahydrate) rhombohedral (heptahydrate) | |||
Hazards | |||
GHS labelling: | |||
Danger | |||
H302+H332, H315, H317, H334, H341, H350, H360D, H372, H410 | |||
P201, P261, P273, P280, P308+P313, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | Non-flammable | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) | 264 mg/kg | ||
Safety data sheet (SDS) | External MSDS | ||
Related compounds | |||
Other cations | Cobalt(II) sulfate Copper(II) sulfate Iron(II) sulfate | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Nickel(II) sulfate, or just nickel sulfate, usually refers to the inorganic compound with the formula NiSO4(H2O)6. This highly soluble blue green coloured salt is a common source of the Ni2+ ion for electroplating.
Approximately 40,000 tonnes were produced in 2005. It is mainly used for electroplating of nickel. [1]
At least seven sulfate salts of nickel(II) are known. These salts differ in terms of their hydration or crystal habit.
The common tetragonal hexahydrate crystallizes from aqueous solution between 30.7 and 53.8 °C. Below these temperatures, a heptahydrate crystallises, and above these temperatures an orthorhombic hexahydrate forms. The yellow anhydrous form, NiSO4, crystallizes in orthorhombic crystal system [2] and in standard pressure decomposes to NiO in temperatures above 640 °C, before reaching the melting point. [3] It melts only at high system pressure, using a constant volume method the melting point was found to be 1210 °C. [4] The anhydrous sulfate is produced by heating the hydrates above 330 °C.
X-ray crystallography measurements show that NiSO4·6H2O consists of the octahedral [Ni(H2O)6]2+ ions. These ions in turn are hydrogen bonded to sulfate ions. [5] Dissolution of the salt in water gives solutions containing the aquo complex [Ni(H2O)6]2+.
All nickel sulfates are paramagnetic.
The salt is usually obtained as a by-product of copper refining. It is also produced by dissolution of nickel metal or nickel oxides in sulfuric acid.
Aqueous solutions of nickel sulfate reacts with sodium carbonate to precipitate nickel carbonate, a precursor to nickel-based catalysts and pigments. [6] Addition of ammonium sulfate to concentrated aqueous solutions of nickel sulfate precipitates Ni(NH4)2(SO4)2·6H2O. This blue-coloured solid is analogous to Mohr's salt, Fe(NH4)2(SO4)2·6H2O. [1]
Nickel sulfate is used in the laboratory. Columns used in polyhistidine-tagging, useful in biochemistry and molecular biology, are regenerated with nickel sulfate. Aqueous solutions of NiSO4·6H2O and related hydrates react with ammonia to give [Ni(NH3)6]SO4 and with ethylenediamine to give [Ni(H2NCH2CH2NH2)3]SO4. The latter is occasionally used as a calibrant for magnetic susceptibility measurements because it has no tendency to hydrate.
Nickel sulfate occurs as the rare mineral retgersite, which is a hexahydrate. The second hexahydrate is known as nickelhexahydrite (Ni,Mg,Fe)SO4·6H2O, which is the monoclinic dimorph of retgersite. The heptahydrate, which is relatively unstable in air, occurs as morenosite. The monohydrate occurs as the very rare mineral dwornikite (Ni,Fe)SO4·H2O.
In 2005–2006, nickel sulfate was the top allergen in patch tests (19.0%). [7] Nickel sulfate is classified as a human carcinogen [8] [9] [10] [11] based on increased respiratory cancer risks observed in epidemiological studies of sulfidic ore refinery workers. [12] In a 2-year inhalation study in F344 rats and B6C3F1 mice, there was no evidence of carcinogenic activity, although increased lung inflammations and bronchial lymph node hyperplasia were observed. [13] These results strongly suggest that there is a threshold for the carcinogenicity of nickel sulfate via inhalation. In a 2-year study with daily oral administration of nickel sulfate hexahydrate to F344 rats, no evidence for increased carcinogenic activity was observed. [14] The human and animal data consistently indicate a lack of carcinogenicity via the oral route of exposure and limit the carcinogenicity of nickel compounds to respiratory tumours after inhalation. [15] Whether these effects are relevant to humans is unclear as epidemiological studies of highly exposed female workers have not shown adverse developmental toxicity effects. [16]
Magnesium sulfate or magnesium sulphate (in English-speaking countries other than the US) is a chemical compound, a salt with the formula MgSO4, consisting of magnesium cations Mg2+ (20.19% by mass) and sulfate anions SO2−4. It is a white crystalline solid, soluble in water but not in ethanol.
Zinc sulfate describes a family of inorganic compounds with the formula ZnSO4(H2O)x. All are colorless solids. The most common form includes water of crystallization as the heptahydrate, with the formula ZnSO4·7H2O. It was historically known as "white vitriol". Zinc sulfate and its hydrates are colourless solids.
In chemistry, water(s) of crystallization or water(s) of hydration are water molecules that are present inside crystals. Water is often incorporated in the formation of crystals from aqueous solutions. In some contexts, water of crystallization is the total mass of water in a substance at a given temperature and is mostly present in a definite (stoichiometric) ratio. Classically, "water of crystallization" refers to water that is found in the crystalline framework of a metal complex or a salt, which is not directly bonded to the metal cation.
Dysprosium(III) chloride (DyCl3), also known as dysprosium trichloride, is a compound of dysprosium and chlorine. It is a white to yellow solid which rapidly absorbs water on exposure to moist air to form a hexahydrate, DyCl3·6H2O. Simple rapid heating of the hydrate causes partial hydrolysis to an oxychloride, DyOCl.
Chromium(III) chloride (also called chromic chloride) is an inorganic chemical compound with the chemical formula CrCl3. It forms several hydrates with the formula CrCl3·nH2O, among which are hydrates where n can be 5 (chromium(III) chloride pentahydrate CrCl3·5H2O) or 6 (chromium(III) chloride hexahydrate CrCl3·6H2O). The anhydrous compound with the formula CrCl3 are violet crystals, while the most common form of the chromium(III) chloride are the dark green crystals of hexahydrate, CrCl3·6H2O. Chromium chlorides find use as catalysts and as precursors to dyes for wool.
Nickel(II) chloride (or just nickel chloride) is the chemical compound NiCl2. The anhydrous salt is yellow, but the more familiar hydrate NiCl2·6H2O is green. Nickel(II) chloride, in various forms, is the most important source of nickel for chemical synthesis. The nickel chlorides are deliquescent, absorbing moisture from the air to form a solution. Nickel salts have been shown to be carcinogenic to the lungs and nasal passages in cases of long-term inhalation exposure.
Vanadyl(IV) sulfate describes a collection of inorganic compounds of vanadium with the formula, VOSO4(H2O)x where 0 ≤ x ≤ 6. The pentahydrate is common. This hygroscopic blue solid is one of the most common sources of vanadium in the laboratory, reflecting its high stability. It features the vanadyl ion, VO2+, which has been called the "most stable diatomic ion".
Nickel(II) oxide is the chemical compound with the formula NiO. It is the principal oxide of nickel. It is classified as a basic metal oxide. Several million kilograms are produced annually of varying quality, mainly as an intermediate in the production of nickel alloys. The mineralogical form of NiO, bunsenite, is very rare. Other nickel(III) oxides have been claimed, for example: Ni
2O
3 and NiO
2, but they have yet to be proven by X-ray crystallography.
Nickel nitrate is the inorganic compound Ni(NO3)2 or any hydrate thereof. The anhydrous form is not commonly encountered, thus "nickel nitrate" usually refers to nickel(II) nitrate hexahydrate. The formula for this species is written in two ways: Ni(NO3)2.6H2O and, more descriptively [Ni(H2O)6](NO3)2. The latter formula indicates that the nickel(II) center is surrounded by six water molecules in this hydrated salt. In the hexahydrate, the nitrate anions are not bonded to nickel. Also known are three other hydrates: Ni(NO3)2.9H2O, Ni(NO3)2.4H2O, and Ni(NO3)2.2H2O. Anhydrous Ni(NO3)2 is also known.
Manganese(II) sulfate usually refers to the inorganic compound with the formula MnSO4·H2O. This pale pink deliquescent solid is a commercially significant manganese(II) salt. Approximately 260,000 tonnes of manganese(II) sulfate were produced worldwide in 2005. It is the precursor to manganese metal and many other chemical compounds. Manganese-deficient soil is remediated with this salt.
Iron(III) sulfate (or ferric sulfate), is a family of inorganic compounds with the formula Fe2(SO4)3(H2O)n. A variety of hydrates are known, including the most commonly encountered form of "ferric sulfate". Solutions are used in dyeing as a mordant, and as a coagulant for industrial wastes. Solutions of ferric sulfate are also used in the processing of aluminum and steel.
Chromium(III) sulfate usually refers to the inorganic compounds with the formula Cr2(SO4)3.x(H2O), where x can range from 0 to 18. Additionally, ill-defined but commercially important "basic chromium sulfates" are known. These salts are usually either violet or green solids that are soluble in water. It is commonly used in tanning leather.
Tutton's salts are a family of salts with the formula M2M'(SO4)2(H2O)6 (sulfates) or M2M'(SeO4)2(H2O)6 (selenates). These materials are double salts, which means that they contain two different cations, M+ and M'2+ crystallized in the same regular ionic lattice. The univalent cation can be potassium, rubidium, cesium, ammonium (NH4), deuterated ammonium (ND4) or thallium. Sodium or lithium ions are too small. The divalent cation can be magnesium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc or cadmium. In addition to sulfate and selenate, the divalent anion can be chromate (CrO42−), tetrafluoroberyllate (BeF42−), hydrogenphosphate (HPO42−) or monofluorophosphate (PO3F2−). Tutton's salts crystallize in the monoclinic space group P21/a. The robustness is the result of the complementary hydrogen-bonding between the tetrahedral anions and cations as well their interactions with the metal aquo complex [M(H2O)6]2+.
Cobalt(II) sulfate is any of the inorganic compounds with the formula CoSO4(H2O)x. Usually cobalt sulfate refers to the hexa- or heptahydrates CoSO4.6H2O or CoSO4.7H2O, respectively. The heptahydrate is a red solid that is soluble in water and methanol. Since cobalt(II) has an odd number of electrons, its salts are paramagnetic.
Nickel(II) bromide is the name for the inorganic compounds with the chemical formula NiBr2(H2O)x. The value of x can be 0 for the anhydrous material, as well as 2, 3, or 6 for the three known hydrate forms. The anhydrous material is a yellow-brown solid which dissolves in water to give blue-green hexahydrate (see picture).
Beryllium sulfate normally encountered as the tetrahydrate, [Be(H2O)4]SO4 is a white crystalline solid. It was first isolated in 1815 by Jons Jakob Berzelius. Beryllium sulfate may be prepared by treating an aqueous solution of many beryllium salts with sulfuric acid, followed by evaporation of the solution and crystallization. The hydrated product may be converted to anhydrous salt by heating at 400 °C.
Nickel compounds are chemical compounds containing the element nickel which is a member of the group 10 of the periodic table. Most compounds in the group have an oxidation state of +2. Nickel is classified as a transition metal with nickel(II) having much chemical behaviour in common with iron(II) and cobalt(II). Many salts of nickel(II) are isomorphous with salts of magnesium due to the ionic radii of the cations being almost the same. Nickel forms many coordination complexes. Nickel tetracarbonyl was the first pure metal carbonyl produced, and is unusual in its volatility. Metalloproteins containing nickel are found in biological systems.
Vanadium(II) sulfate describes a family of inorganic compounds with the formula VSO4(H2O)x where 0 ≤ x ≤ 7. The hexahydrate is most commonly encountered. It is a violet solid that dissolves in water to give air-sensitive solutions of the aquo complex. The salt is isomorphous with [Mg(H2O)6]SO4. Compared to the V–O bond length of 191 pm in [V(H2O)6]3+, the V–O distance is 212 pm in the [V(H2O)6]SO4. This nearly 10% elongation reflects the effect of the lower charge, hence weakened electrostatic attraction.
The Nickel oxyacid salts are a class of chemical compounds of nickel with an oxyacid. The compounds include a number of minerals and industrially important nickel compounds.
Gallium(III) sulfate refers to the chemical compound, a salt, with the formula Ga2(SO4)3, or its hydrates Ga2(SO4)3·xH2O. Gallium metal dissolves in sulfuric acid to form solutions containing [Ga(OH2)6]3+ and SO42− ions. The octadecahydrate Ga2(SO4)3·18H2O crystallises from these solutions at room temperature. This hydrate loses water in stages when heated, forming the anhydrate Ga2(SO4)3 above 150 °C and completely above 310 °C. Anhydrous Ga2(SO4)3 is isostructural with iron(III) sulfate, crystallizing in the rhombohedral space group R3.