Chemistry:Raney nickel

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Raney nickel
Light-gray powder on a glass dish
Dry activated Raney nickel
Identifiers
UNII
Properties
Appearance Light-gray powder
Hazards
GHS pictograms GHS02: FlammableGHS07: HarmfulGHS08: Health hazard
H250, H317, H351, H372, H412
P210, P273, P280, P302
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Raney nickel /ˈreɪniː ˈnɪkəl/, also called spongy nickel,[1] is a fine-grained solid composed mostly of nickel derived from a nickel–aluminium alloy.[2][3] Several grades are known, of which most are gray solids. Some are pyrophoric, but most are used as air-stable slurries. Raney nickel is used as a reagent and as a catalyst in organic chemistry. It was developed in 1926 by American engineer Murray Raney for the hydrogenation of vegetable oils.[4][5] Raney is a registered trademark of W. R. Grace and Company. Other major producers are Evonik and Johnson Matthey.

Preparation

Alloy preparation

Shiny metal can with hazard labels.
Raney nickel is pyrophoric and must be handled with care. This shipping container is filled with vermiculite to protect the sealed bottle inside.

The Ni–Al alloy is prepared by dissolving nickel in molten aluminium followed by cooling ("quenching"). Depending on the Ni:Al ratio, quenching produces a number of different phases. During the quenching procedure, small amounts of a third metal, such as zinc or chromium, are added to enhance the activity of the resulting catalyst. This third metal is called a "promoter".[6] The promoter changes the mixture from a binary alloy to a ternary alloy, which can lead to different quenching and leaching properties during activation.

Activation

In the activation process, the alloy, usually as a fine powder, is treated with a concentrated solution of sodium hydroxide.[3] The simplified leaching reaction is given by the following chemical equation:

2 Al + 2 NaOH + 6 H2O → 2 Na[Al(OH)4] + 3 H2

The formation of sodium aluminate (Na[Al(OH)4]) requires that solutions of high concentration of sodium hydroxide be used to avoid the formation of aluminium hydroxide, which otherwise would precipitate as bayerite.[6] Hence sodium hydroxide solutions with concentrations of up to 5 M are used.

The temperature used to leach the alloy has a marked effect on the properties of the catalyst. Commonly, leaching is conducted between 70 and 100 °C. The surface area of Raney nickel (and related catalysts in general) tends to decrease with increasing leaching temperature.[7] This is due to structural rearrangements within the alloy that may be considered analogous to sintering, where alloy ligaments would start adhering to each other at higher temperatures, leading to the loss of the porous structure.[citation needed]

During the activation process, Al is leached out of the NiAl3 and Ni2Al3 phases that are present in the alloy, while most of the Ni remains, in the form of NiAl. The removal of Al from some phases but not others is known as "selective leaching". The NiAl phase has been shown to provide the structural and thermal stability of the catalyst. As a result, the catalyst is quite resistant to decomposition ("breaking down", commonly known as "aging").[7] This resistance allows Raney nickel to be stored and reused for an extended period; however, fresh preparations are usually preferred for laboratory use.[8] For this reason, commercial Raney nickel is available in both "active" and "inactive" forms.

Before storage, the catalyst can be washed with distilled water at ambient temperature to remove remaining sodium aluminate. Oxygen-free (degassed) water is preferred for storage to prevent oxidation of the catalyst, which would accelerate its aging process and result in reduced catalytic activity.[6]

Properties

A graph of temperature vs. weight percent of nickel in aluminium, showing stability regions of various AlNi, Al3Ni, AlNi3 and Al3Ni2 phases
Phase diagram of the Ni–Al system, showing relevant phases
SEM of Raney nickel catalyst in which crystals of 1-50µm are seen.
A close-up of Raney nickel. Small cracks of approximately 1-100 nm width are seen within the crystals, causing the increased surface area.

Macroscopically, Raney nickel is a finely divided, grey powder. Microscopically, each particle of this powder is a three-dimensional mesh, with pores of irregular size and shape, the vast majority of which are created during the leaching process. Raney nickel is notable for being thermally and structurally stable, as well as having a large Brunauer-Emmett-Teller (BET ) surface area. These properties are a direct result of the activation process and contribute to a relatively high catalytic activity.[citation needed]

The surface area is typically determined by a BET measurement using a gas that is preferentially adsorbed on metallic surfaces, such as hydrogen. Using this type of measurement, almost all the exposed area in a particle of the catalyst has been shown to have Ni on its surface.[6] Since Ni is the active metal of the catalyst, a large Ni surface area implies a large surface is available for reactions to occur simultaneously, which is reflected in an increased catalyst activity. Commercially available Raney nickel has an average Ni surface area of 100 m2 per gram of catalyst.[6]

A high catalytic activity, coupled with the fact that hydrogen is absorbed within the pores of the catalyst during activation, makes Raney nickel a useful catalyst for many hydrogenation reactions. Its structural and thermal stability (i.e., it does not decompose at high temperatures) allows its use under a wide range of reaction conditions.[9][10] Additionally, the solubility of Raney nickel is negligible in most common laboratory solvents, with the exception of mineral acids such as hydrochloric acid, and its relatively high density (about 6.5 g cm−3)[1] also facilitates its separation from a liquid phase after a reaction is completed.

Applications

Raney nickel is used in a large number of industrial processes and in organic synthesis because of its stability and high catalytic activity at room temperature.[6][11][12]

Industrial applications

In a commercial application, Raney nickel is used as a catalyst for the hydrogenation of benzene to cyclohexane. Other heterogeneous catalysts, such as those using platinum group elements are used in some cases. Platinum metals tend to be more active, requiring milder temperatures, but they are more expensive than Raney nickel.[13] The cyclohexane thus produced may be used in the synthesis of adipic acid, a raw material used in the industrial production of polyamides such as nylon.[14]

Chemical reaction. Benzene converts to cyclohexane under the action of hydrogen and Raney nickel. Cyclohexane then oxidizes to adipic acid.
using Raney nickel catalyzes the hydrogenation benzene to cyclohexane for the production of nylon precursors.

Other industrial applications of Raney nickel include the conversion of:

Applications in organic synthesis

Desulfurization

Raney nickel is used in organic synthesis for desulfurization. For example, thioacetals will be reduced to hydrocarbons in the last step of the Mozingo reduction:[14][15]

Chemical reaction: Thioacetal breaks into ethane, nickel sulfide and a hydrocarbon under the action of hydrogen and Raney nickel.
Example of desulfurization of thioacetals using Raney nickel

Thiols,[16] and sulfides[17] can be removed from aliphatic, aromatic, or heteroaromatic compounds. Likewise, Raney nickel will remove the sulfur of thiophene to give a saturated alkane.[18]

Chemical reaction: Reduction of thiophene under the action of hydrogen, Raney nickel and methanol
Reduction of thiophene by Raney nickel

Reduction of functional groups

It is typically used in the reduction of compounds with multiple bonds, such as alkynes, alkenes,[19] nitriles,[20] dienes, aromatics[21] and carbonyl-containing compounds. Additionally, Raney nickel will reduce heteroatom-heteroatom bonds, such as hydrazines,[22] nitro groups, and nitrosamines.[23] It has also found use in the reductive alkylation of amines[24] and the amination of alcohols.

When reducing a carbon-carbon double bond, Raney nickel will add hydrogen in a syn fashion.[14]

Related catalysts

Raney cobalt has also been described.

In contrast to the pyrophoric nature of some forms of Raney nickel, nickel silicide-based catalysts represent potentially safer alternatives.[25]

Safety

A square orange sticker with a flame picture.
Raney nickel is flammable.
A square orange sticker with a black cross on it.
Nickel metal is classified as "Harmful".

Due to its large surface area and high volume of contained hydrogen gas, dry, activated Raney nickel is a pyrophoric material that requires handling under an inert atmosphere. Raney nickel is typically supplied as a 50% slurry in water. Even after reaction, residual Raney nickel contains significant amounts of hydrogen gas and may spontaneously ignite when exposed to air.[26]

Additionally, acute exposure to Raney nickel may cause irritation of the respiratory tract and nasal cavities, and causes pulmonary fibrosis if inhaled. Ingestion may lead to convulsions and intestinal disorders. It can also cause eye and skin irritation. Chronic exposure may lead to pneumonitis and other signs of sensitization to nickel, such as skin rashes ("nickel itch").[27]

NFPA 704
fire diamond
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineHealth code 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineReactivity code 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no codeNFPA 704 four-colored diamond
3
1
1

Nickel is also rated as being a possible human carcinogen by the IARC (Group 2B, EU category 3) and teratogen, while the inhalation of fine aluminium oxide particles is associated with Shaver's disease.

Development

Murray Raney graduated as a mechanical engineer from the University of Kentucky in 1909. In 1915 he joined the Lookout Oil and Refining Company in Tennessee and was responsible for the installation of electrolytic cells for the production of hydrogen which was used in the hydrogenation of vegetable oils. During that time the industry used a nickel catalyst prepared from nickel(II) oxide. Believing that better catalysts could be produced, around 1921 he started to perform independent research while still working for Lookout Oil. In 1924 a 1:1 ratio Ni/Si alloy was produced, which after treatment with sodium hydroxide, was found to be five times more active than the best catalyst used in the hydrogenation of cottonseed oil. A patent for this discovery was issued in December 1925.[28]

Subsequently, Raney produced a 1:1 Ni/Al alloy following a procedure similar to the one used for the nickel-silicon catalyst. He found that the resulting catalyst was even more active and filed a patent application in 1926.[29] This is now a common alloy composition for modern Raney nickel catalysts.[2] Other common alloy compositions include 21:29 Ni/Al and 3:7 Ni/Al. Both the activity and preparation protocols for these catalysts vary.[2][30]

Following the development of Raney nickel, other alloy systems with aluminium were considered, of which the most notable include copper, ruthenium and cobalt.[31] Further research showed that adding a small amount of a third metal to the binary alloy would promote the activity of the catalyst. Some widely used promoters are zinc, molybdenum and chromium. An alternative way of preparing enantioselective Raney nickel has been devised by surface adsorption of tartaric acid.[32]

See also

References

  1. ↑ 1.0 1.1 "Spongy Nickel". European Space Agency. http://www.spaceflight.esa.int/impress/text/education/Catalysis/Spongy.html. 
  2. ↑ 2.0 2.1 2.2 2.3 Nishimura, Shigeo (2001). Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis (1st ed.). New York: Wiley-Interscience. pp. 7–19. ISBN 9780471396987. https://books.google.com/books?id=RjZRAAAAMAAJ. 
  3. ↑ 3.0 3.1 Billica, Harry; Adkins, Homer (1949). "Cataylst, Raney Nickel, W6 (with high contents of aluminum and adsorbed hydrogen)". Organic Syntheses 29: 24. doi:10.15227/orgsyn.029.0024. http://www.orgsyn.org/demo.aspx?prep=CV3P0176. ; Collective Volume, 3, pp. 176 
  4. ↑ See:
    • Raney, Murray, "Method of producing finely-divided nickel," U.S. patent 1,628,190 (filed: 14 May 1926 ; issued: 10 May 1927).
    • M. S. Wainwright, "3.2 Skeletal metal catalysts" in: Gerhard Ertl, Helmut Knözinger, and Jens Weitkamp, ed.s, Preparaton of Solid Catalysts (Weinheim, Federal Republic of Germany: Wiley-VCH Verlag, 1999), pages 28–29.
  5. ↑ Yang, Teng-Kuei; Lee, Dong-Sheng; Haas, Julia (2005). "Raney Nickel". Encyclopedia of Reagents for Organic Synthesis. New York: John Wiley & Sons. doi:10.1002/047084289X.rr001.pub2. ISBN 0471936235. 
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 Ertl, Gerhard; Knözinger, Helmut (1997). Preparation of Solid Catalysts. Wiley. pp. 30–34. ISBN 3-527-29826-6. https://books.google.com/books?id=Yb38DM1IoAsC&pg=PA30. 
  7. ↑ 7.0 7.1 Smith, A.J.; Trimm, D.L. (2005). "The preparation of skeletal catalysts". Annu. Rev. Mater. Res. 35: 127. doi:10.1146/annurev.matsci.35.102303.140758. 
  8. ↑ M. Guisnet, ed (1993). Heterogeneous catalysis and fine chemicals III: proceedings of the 3rd international symposium. Elsevier. p. 69. ISBN 0-444-89063-7. https://books.google.com/books?id=AwyJ6IEtaBsC&pg=PA69. 
  9. ↑ Crawford, Gerald (April 2003). "Exotic Alloy Finds Niche". Nickel magazine. http://www.nidi.org/index.cfm/ci_id/12317.htm. 
  10. ↑ Carruthers, W (1986). Some modern methods of organic synthesis. Cambridge University Press. pp. 413–414. ISBN 0-521-31117-9. https://books.google.com/books?id=ti7yMYYW7CMC&pg=PA413. 
  11. ↑ Hauptmann, Heinrich; Walter, Wolfgang Ferdinand (1962). "The Action of Raney Nickel on Organic Sulfur Compounds.". Chem. Rev. 62 (5): 347. doi:10.1021/cr60219a001. 
  12. ↑ "Raney nickel usage in Organic Syntheses". 2005. http://www.orgsyn.org/orgsyn/chemname.asp?nameID=33759. 
  13. ↑ Campbell, M. Larry (2011). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_209.pub2. 
  14. ↑ 14.0 14.1 14.2 Solomons, T.W. Graham; Fryhle, Craig B. (2004). Organic Chemistry. Wiley. ISBN 0-471-41799-8. https://archive.org/details/organicchemistry00solo_0. 
  15. ↑ Jonathan Clayden; Nick Greeves; Stuart Warren (2012). Organic Chemistry (2 ed.). Oxford University Press. ISBN 9780199270293. 
  16. ↑ Graham, A. R.; Millidge, A. F.; Young, D. P. (1954). "Oxidation products of diisobutylene. Part III. Products from ring-opening of 1,2-epoxy-2,4,4-trimethylpentane". Journal of the Chemical Society (Resumed): 2180. doi:10.1039/JR9540002180. 
  17. ↑ Gassman, P. G.; van Bergen, T. J. (1988). "Indoles from anilines: Ethyl 2-methylindole-5-carboxylate". Organic Syntheses. doi:10.15227/orgsyn.056.0072. ; Collective Volume, 6, pp. 601 
  18. ↑ Hoegberg, Hans Erik; Hedenstroem, Erik; Faegerhag, Jonas; Servi, Stefano (1992). "Enantioselective synthesis of (S)-2-methyl-1-alkanols via bakers' yeast mediated reduction of 2-methyl-3-(2-thiophene)propenals". J. Org. Chem. 57 (7): 2052–2059. doi:10.1021/jo00033a028. 
  19. ↑ Page, G. A.; Tarbell, D. S. (1963). "β-(o-Carboxyphenyl)propionic acid". Organic Syntheses 34: 8. doi:10.15227/orgsyn.034.0008. http://www.orgsyn.org/demo.aspx?prep=CV4P0136. ; Collective Volume, 4, pp. 136 
  20. ↑ Robinson, H. C.; Snyder, H. R. (1955). "β-Phenylethylamine". Organic Syntheses 23: 71. doi:10.15227/orgsyn.023.0071. http://www.orgsyn.org/demo.aspx?prep=CV3P0720. ; Collective Volume, 3, pp. 720 
  21. ↑ Schwenk, E.; Papa, D.; Hankin, H.; Ginsberg, H. (1955). "γ-n-Propylbutyrolactone and β-(Tetrahydrofuryl)propionic acid". Organic Syntheses 27: 68. doi:10.15227/orgsyn.027.0068. http://www.orgsyn.org/demo.aspx?prep=CV3P0742. ; Collective Volume, 3, pp. 742 
  22. ↑ Alexakis, Alex; Lensen, Nathalie; Mangeney, Pierre (1991). "Ultrasound-Assisted Cleavage of N-N Bonds in Hydrazines by Raney Nickel". Synlett 1991 (9): 625–626. doi:10.1055/s-1991-20818. 
  23. ↑ Enders, D.; Pieter, R.; Renger, B.; Seebach, D. (1988). "Nucleophilic α-sec-aminoalkylation: 2-(diphenylhydroxymethyl)pyrrolidene". Organic Syntheses 58: 113. doi:10.15227/orgsyn.058.0113. http://www.orgsyn.org/demo.aspx?prep=CV6P0542. ; Collective Volume, 6, pp. 542 
  24. ↑ Rice, R. G.; Kohn, E. J. (1963). "N,N'-Diethylbenzidene". Organic Syntheses 36: 21. doi:10.15227/orgsyn.036.0021. http://www.orgsyn.org/demo.aspx?prep=CV4P0283. ; Collective Volume, 4, pp. 283 
  25. ↑ P. Ryabchuk, G. Agostini, M.-M. Pohl, H. Lund, A. Agapova, H. Junge, K. Junge and M. Beller, Sci. Adv., 2018, 4, eaat0761, https://www.science.org/doi/10.1126/sciadv.aat0761
  26. ↑ Armour, M.-A (2003). Hazardous laboratory chemicals disposal guide. CRC Press. p. 331. ISBN 1-56670-567-3. https://books.google.com/books?id=geK5gjEn3hkC&pg=PA331. 
  27. ↑ "Nickel aluminide MSDS". Electronic Space Products International. 1994. http://www.msdshazcom.com/MSDS/E/espi/Nickel%20Aluminide%20NiAl.pdf. [yes|permanent dead link|dead link}}]
  28. ↑ Murray Raney, "Method of Preparing Catalytic Material", US patent 1563587, issued 1925-12-01 (Raney's original nickel-silicon catalyst)
  29. ↑ Murray Raney, "Method of Producing Finely-Divided Nickel", US patent 1628190, issued 1927-05-10
  30. ↑ Urushibara, Yoshiyuki; Nishimura, Shigeo (1957). "A Method for the Preparation of the Raney Nickel Catalyst with a Greater Activity". Bull. Chem. Soc. Jpn. 30 (2): 199. doi:10.1246/bcsj.30.199. 
  31. ↑ Augustine, Robert L. (1996). Heterogeneous catalysis for the synthetic chemist. CRC Press. pp. 248–249. ISBN 0-8247-9021-9. https://books.google.com/books?id=Nam8OVqKaXIC&pg=PA250. 
  32. ↑ Bakker, M. L.; Young, D. J.; Wainwright, M. S. (1988). "Selective leaching of NiAl3 and Ni2Al3 intermetallics to form Raney nickels". J. Mater. Sci. 23 (11): 3921–3926. doi:10.1007/BF01106814. 

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