Dmg Chemical Formula
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- Dimethylglyoxime
- Dmg Chemical Formula
Names | |
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Systematic IUPAC name | |
Identifiers | |
3D model (JSmol) |
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ECHA InfoCard | 100.006.147 |
EC Number | |
PubChemCID | |
CompTox Dashboard(EPA) | |
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Properties | |
C4H6NiO4 | |
Molar mass | 176.781 g·mol−1 |
Appearance | Green Solid |
Odor | slight acetic acid |
Density | 1.798 g/cm3 (anhydrous) 1.744 g/cm3 (tetrahydrate) |
Melting point | decomposes when heated [1][2] |
Easily soluble in cold water, hot water | |
Solubility | Soluble in methanol insoluble in diethyl ether, n-octanol |
+4,690.0·10−6 cm3/mol | |
Structure | |
monoclinic | |
P21/c | |
α = 90°, β = 93.6°, γ = 90°[3] | |
Lattice volume (V) | 471.5 |
2 | |
distorted octahedral | |
Hazards | |
NFPA 704 (fire diamond) | |
Lethal dose or concentration (LD, LC): | |
350 mg/kg (rat, oral) 410 mg/kg (mouse, oral)[4] | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references |
Material Safety Data Sheet Dimethylglyoxime, 1% Alcoholic - 2 - Ingestion: May cause irritation of the digestive tract. Symptoms may include headache, excitement, fatigue. Enter a chemical formula to calculate its molar mass and elemental composition: Molar mass of Ni(dmg)2 is 288.9146 g/mol Formula in Hill system is C8H14N4NiO4.
Nickel(II) acetate is the name for the coordination compounds with the formula Ni(CH3CO2)2·x H2O where x can be 0, 2, and 4. The green tetrahydrate Ni(CH3CO2)2·4 H2O is most common. It is used for electroplating.
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Synthesis and structure[edit]
The compound can be prepared by treating nickel or nickel(II) carbonate with acetic acid:
- NiCO3 + 2 CH3CO2H + 3 H2O → Ni(CH3CO2)2·4 H2O + CO2
The green tetrahydrate has been shown by X-ray crystallography to adopt an octahedral structure, the central nickel centre being coordinated by four water molecules and two acetate ligands.[5] It may be dehydrated in vacuo, by reaction with acetic anhydride,[6] or by heat.[7]
Dmg Chemical Formula Calculator
Safety[edit]
Nickel salts are carcinogenic and irritate the skin.
References[edit]
- ^M. A. Mohamed, S. A. Halawy, M. M. Ebrahim: 'Non-isothermal decomposition of nickel acetate tetrahydrate', in: Journal of Analytical and Applied Pyrolysis, 1993, 27 (2), S. 109–110. doi:10.1016/0165-2370(93)80002-H.
- ^G. A. M. Hussein, A. K. H. Nohman, K. M. A. Attyia: 'Characterization of the decomposition course of nickel acetate tetrahydrate in air', in: Journal of Thermal Analysis and Calorimetry, 1994, 42, S. 1155–1165; doi:10.1007/BF02546925.
- ^Downie, T. C.; Harrison, W.; Raper, E. S.; Hepworth, M. A. (15 March 1971). 'A three-dimensional study of the crystal structure of nickel acetate tetrahydrate'. Acta Crystallographica Section B. 27 (3): 706–712. doi:10.1107/S0567740871002802.
- ^'Nickel metal and other compounds (as Ni)'. Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- ^Van Niekerk, J. N.; Schoening, F. R. L. (1953). 'The crystal structures of nickel acetate, Ni(CH3COO)2·4H2O, and cobalt acetate, Co(CH3COO)2·4H2O'. Acta Crystallogr.6 (7): 609–612. doi:10.1107/S0365110X5300171X.
- ^Lascelles, Keith; Morgan, Lindsay G.; Nicholls, David; Beyersmann, Detmar (2005). 'Nickel Compounds'. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_235.pub2.
- ^Tappmeyer, W. P.; Davidson, Arthur W. (1963). 'Cobalt and Nickel Acetates in Anhydrous Acetic Acid'. Inorg. Chem.2 (4): 823–825. doi:10.1021/ic50008a039.
AcOH | He | ||||||||||||||||
LiOAc | Be(OAc)2 BeAcOH | B(OAc)3 | AcOAc ROAc | NH4OAc | AcOOH | FAc | Ne | ||||||||||
NaOAc | Mg(OAc)2 | Al(OAc)3 ALSOL Al(OAc)2OH Al2SO4(OAc)4 | Si | P | S | ClAc | Ar | ||||||||||
KOAc | Ca(OAc)2 | Sc(OAc)3 | Ti(OAc)4 | VO(OAc)3 | Cr(OAc)2 Cr(OAc)3 | Mn(OAc)2 Mn(OAc)3 | Fe(OAc)2 Fe(OAc)3 | Co(OAc)2, Co(OAc)3 | Ni(OAc)2 | Cu(OAc)2 | Zn(OAc)2 | Ga(OAc)3 | Ge | As(OAc)3 | Se | BrAc | Kr |
RbOAc | Sr(OAc)2 | Y(OAc)3 | Zr(OAc)4 | Nb | Mo(OAc)2 | Tc | Ru(OAc)2 Ru(OAc)3 Ru(OAc)4 | Rh2(OAc)4 | Pd(OAc)2 | AgOAc | Cd(OAc)2 | In | Sn(OAc)2 Sn(OAc)4 | Sb(OAc)3 | Te | IAc | Xe |
CsOAc | Ba(OAc)2 | Hf | Ta | W | Re | Os | Ir | Pt(OAc)2 | Au | Hg2(OAc)2, Hg(OAc)2 | TlOAc Tl(OAc)3 | Pb(OAc)2 Pb(OAc)4 | Bi(OAc)3 | Po | At | Rn | |
Fr | Ra | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Nh | Fl | Mc | Lv | Ts | Og | |
↓ | |||||||||||||||||
La(OAc)3 | Ce(OAc)x | Pr | Nd | Pm | Sm(OAc)3 | Eu(OAc)3 | Gd(OAc)3 | Tb | Dy(OAc)3 | Ho(OAc)3 | Er | Tm | Yb(OAc)3 | Lu(OAc)3 | |||
Ac | Th | Pa | UO2(OAc)2 | Np | Pu | Am | Cm | Bk | Cf | Es | Fm | Md | No | Lr |
Names | |
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IUPAC name | |
Other names Nickel hydroxide, Theophrastite | |
Identifiers | |
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ChemSpider | |
ECHA InfoCard | 100.031.813 |
EC Number |
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RTECS number | |
CompTox Dashboard(EPA) | |
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Properties | |
Ni(OH)2 | |
Molar mass | 92.724 g/mol (anhydrous) 110.72 g/mol (monohydrate) |
Appearance | green crystals |
Density | 4.10 g/cm3 |
Melting point | 230 °C (446 °F; 503 K) (anhydrous, decomposes) |
0.13 g/L | |
+4500.0·10−6 cm3/mol | |
Structure[1] | |
hexagonal, hP3 | |
P3m1, No. 164 | |
α = 90°, β = 90°, γ = 120° | |
Thermochemistry | |
79 J·mol−1·K−1[2] | |
Std enthalpy of formation(ΔfH⦵298) | −538 kJ·mol−1[2] |
Hazards | |
Safety data sheet | External SDS |
GHS pictograms | [3] |
GHS Signal word | Danger[3] |
H302, H332, H315, H334, H317, H341, H350, H360, H372[3] | |
P260, P284, P201, P280, P405, P501[3] | |
Lethal dose or concentration (LD, LC): | |
1515 mg/kg (oral, rat) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references |
Nickel(II) hydroxide is the inorganic compound with the formula Ni(OH)2. It is an apple-green solid that dissolves with decomposition in ammonia and amines and is attacked by acids. It is electroactive, being converted to the Ni(III) oxy-hydroxide, leading to widespread applications in rechargeable batteries.[4]
Properties[edit]
Nickel(II) hydroxide has two well-characterized polymorphs, α and β. The α structure consists of Ni(OH)2 layers with intercalated anions or water.[5][6] The β form adopts a hexagonal close-packed structure of Ni2+ and OH− ions.[5][6] In the presence of water, the α polymorph typically recrystallizes to the β form.[5][7] In addition to the α and β polymorphs, several γ nickel hydroxides have been described, distinguished by crystal structures with much larger inter-sheet distances.[5]
The mineral form of Ni(OH)2, theophrastite, was first identified in the Vermion region of northern Greece, in 1980. It is found naturally as a translucent emerald-green crystal formed in thin sheets near the boundaries of idocrase or chlorite crystals.[8] A nickel-magnesium variant of the mineral, (Ni,Mg)(OH)2 had been previously discovered at Hagdale on the island of Unst in Scotland.[9]
Dmg Chemical Formula Chart
Reactions[edit]
Nickel(II) hydroxide is frequently used in electrical car batteries.[6] Specifically, Ni(OH)2 readily oxidizes to nickel oxyhydroxide, NiOOH, in combination with a reduction reaction, often of a metal hydride (reaction 1 and 2).[10]
Dmg Chemical Formula 2
Reaction 1 Ni(OH)2 + OH− → NiO(OH) + H2O + e−
Reaction 2 M + H2O + e− → MH + OH−
Net Reaction (in H2O)Ni(OH)2 + M → NiOOH + MH
Of the two polymorphs, α-Ni(OH)2 has a higher theoretical capacity and thus is generally considered to be preferable in electrochemical applications. However, it transforms to β-Ni(OH)2 in alkaline solutions, leading to many investigations into the possibility of stabilized α-Ni(OH)2 electrodes for industrial applications.[7]
Synthesis[edit]
The synthesis entails treating aqueous solutions of nickel(II) salts with potassium hydroxide.[11]
Toxicity[edit]
The Ni2+ ion is a known carcinogen. Toxicity and related safety concerns have driven research into increasing the energy density of Ni(OH)2 electrodes, such as the addition of calcium or cobalt hydroxides.[4]
See also[edit]
Dimethylglyoxime
References[edit]
- ^Enoki, Toshiaki; Tsujikawa, Ikuji (1975). 'Magnetic Behaviours of a Random Magnet, NipMg(1-p)(OH2)'. Journal of the Physical Society of Japan. 39 (2): 317. doi:10.1143/JPSJ.39.317.
- ^ abZumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22. ISBN978-0-618-94690-7.
- ^ abcd'Nickel Hydroxide'. American Elements. Retrieved 2018-08-30.
- ^ abChen, J.; Bradhurst, D.H.; Dou, S.X.; Liu, H.K. (1999). 'Nickel Hydroxide as an Active Material for the Positive Electrode in Rechargeable Alkaline Batteries'. J. Electrochem. Soc. 146 (10): 3606–3612. doi:10.1149/1.1392522.
- ^ abcdOliva, P.; Leonardi, J.; Laurent, J.F. (1982). 'Review of the structure and the electrochemistry of nickel hydroxides and oxy-hydroxides'. Journal of Power Sources. 8 (2): 229–255. doi:10.1016/0378-7753(82)80057-8.
- ^ abcJeevanandam, P.; Koltypin, Y.; Gedanken, A. (2001). 'Synthesis of Nanosized α-Nickel Hydroxide by a Sonochemical Method'. Nano Letters. 1 (5): 263–266. doi:10.1021/nl010003p.
- ^ abShukla, A.K.; Kumar, V.G.; Munichandriah, N. (1994). 'Stabilized α-Ni(OH)2 as Electrode Material for Alkaline Secondary Cells'. J. Electrochem. Soc. 141 (11): 2956–2959. doi:10.1149/1.2059264.
- ^Marcopoulos, T.; Economou, M. (1980). 'Theophrastite, Ni(OH)2, a new mineral from northern Greece'(PDF). American Mineralogist. 66: 1020–1021.
- ^Livingston, A.; Bish, D. L. (1982). 'On the new mineral theophrastite, a nickel hydroxide, from Unst, Shetland, Scotland'(PDF). Mineralogical Magazine. 46 (338): 1. doi:10.1180/minmag.1982.046.338.01.
- ^Ovshinsky, S.R.; Fetcenko, M.A.; Ross, J. (1993). 'A nickel metal hydride battery for electric vehicles'. Science. 260 (5105): 176–181. doi:10.1126/science.260.5105.176. PMID17807176.
- ^Glemser, O. (1963) 'Nickel(II) Hydroxide' in 'Handbook of Preparative Inorganic Chemistry, 2nd ed. G. Brauer (ed.), Academic Press, NY. Vol. 1. p. 1549.