US3563787A - Aluminum plating process - Google Patents

Aluminum plating process Download PDF

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Publication number
US3563787A
US3563787A US765636A US3563787DA US3563787A US 3563787 A US3563787 A US 3563787A US 765636 A US765636 A US 765636A US 3563787D A US3563787D A US 3563787DA US 3563787 A US3563787 A US 3563787A
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United States
Prior art keywords
aluminum
substrate
catalyst
aluminum hydride
coating
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US765636A
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English (en)
Inventor
Roger G Schneggenburger
Reinhold Hellmann
Kenneth O Groves
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Dow Chemical Co
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Dow Chemical Co
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    • G—PHYSICS
    • G04—HOROLOGY
    • G04B—MECHANICALLY-DRIVEN CLOCKS OR WATCHES; MECHANICAL PARTS OF CLOCKS OR WATCHES IN GENERAL; TIME PIECES USING THE POSITION OF THE SUN, MOON OR STARS
    • G04B37/00—Cases
    • G04B37/14—Suspending devices, supports or stands for time-pieces insofar as they form part of the case

Definitions

  • the process comprises depositing an aluminum hydride decomposition metal catalyst on said substrate; depositing an aluminum hydride material on said substrate in contact with said catalyst; immersing the substrate in a heated inert liquid bath containing a dissolved resin overcoating material thereby decomposing said aluminum hydride material and providing a metallic aluminum coating on said substrate; removing said aluminum coated substrate from said bath and removing the inert liquid to provide a resin overcoat on said metallic aluminum coating.
  • a substrate which has been coated with a thin aluminum film is usually also coated with a resin overcoating, e.g., lacquer, to protect the soft aluminum from scratches, tarnishing and to preserve the mirror-like surface.
  • a resin overcoating e.g., lacquer
  • the present invention allows for the deposition of both an aluminum and a protection overcoat at lower temperatures, with more precise control over the reaction conditions than heretofore possible and also decreases the number of operational steps usually required.
  • the present invention comprises depositing on a substrate a transition metal catalyst capable of decomposing aluminum hydrides to form metallic aluminum coatings at a relatively low temperature; depositing on said substrate in the presence of the catalyst an aluminum hydride compound; immersing said catalyst and aluminum hydride coated substrate in a heated inert liquid bath containing a dissolved overcoating substance; maintaining the substrate in the bath to decompose the aluminum hydride compound, thereby forming a metallic aluminum coating on the substrate; removing the aluminum coated substrate from the bath and removing the inert liquid to deposit an overcoat consisting of the resin overcoating substance.
  • substantially any solid material is suitable as a substrate.
  • metals such as iron, magnesium, brass and copper, polymers such as polyolefins, polyamides, polyesters and polymeric fiuorocarbons, glass, paper, cloth, carbon and graphite, wood, ceramics and the like can all be plated with aluminum and overcoated by the process of this invention.
  • the nature of the surface being plated determines to a large extent the brightness of the aluminum plate.
  • the use of a smooth, nonporous surface such as found on most metals and some polymer films produces a brighter plate than a relatively porous surface such as those encountered with paper or cloth.
  • aluminum hydride is used herein in its broad sense and is meant to include any hydride compound which contains at least one aluminum atom to which at least one hydrogen atom is directly bonded and includes both the solvated and non-solvated forms of those aluminum hydrides occurring in both forms. Included, therefore, are aluminum trihydride, the substituted aluminum hydrides such as those having the empirical formula AlH X wherein X is a halogen, an OR group or an R group (wherein R is an alkyl, substituted alkyl, aryl or substituted aryl group) and n has a numerical value equal to or less than 3.
  • complex aluminum hydrides such as LiAlH NaAlH Mg(AlH and the like and complex substituted aluminum hydrides such as those having the empirical formula M(All-I,,,X wherein X has the definition given above, In has a numerical value equal to or less than 4 and M is a metal or mixture of metals, preferably an alkali or alkaline earth metal and a has a numerical value equal to the valence of M.
  • M is a metal or mixture of metals, preferably an alkali or alkaline earth metal and a has a numerical value equal to the valence of M.
  • the relatively simple aluminum hydrides containing at least two hydrogen atoms attached to the aluminum e.g., AlH AlH Br, LiAlH and the like. Mixtures of the various aluminum hydrides may also be employed.
  • the aluminum hydride in solvated form.
  • Compounds known to solvate or form complexes With the aluminum hydrides include ethers and other oxygen-containing organic compounds, and compounds containing a functional group such as divalent sulfur atom, or trivalent nitrogen or trivalent phosphorous atom which is capable of allowing the solvation of an aluminum hydride with such compound. It is usually preferred that the solvate be an etherate and a wide variety of ethers containing from about 2 to about 20 carbon atoms are suitable.
  • the lower aliphatic ethers such as ethyl, propyl, or butyl ethers are employed but those containing an aromatic group such as methylphenyl ether, ethylphenyl ethers, propylphenyl ether or the alicyclic ethers such as tetrahydrofuran and the like may be employed.
  • any solvent or mixture of solvents or suspending agents for the aluminum hydride may be employed which will not react with the aluminum hydride beyond the formation of a complex or solvate.
  • Suitable solvents include aromatic hydrocarbons such as benzene, toluene and xylene, aliphatic hydrocarbons such as hexane, ethers, tertiary amines and the like.
  • such aluminum hydrides may be prepared in situ simultaneously with the plating step by employing aluminum hydride-forming reactants such as mixtures of lithium aluminum hydride and aluminum chloride, or sodium aluminum hydride and aluminum bromide, or the like.
  • aluminum hydride-forming reactants such as mixtures of lithium aluminum hydride and aluminum chloride, or sodium aluminum hydride and aluminum bromide, or the like.
  • a metal halide such as LiCl, MgCl or AlCl together with the aluminum hydride is not detrimental to the plating reaction.
  • Transition metal decomposition catalysts useful herein are compounds of the metals occurring in Groups Nb and Vb of the periodic table. In instances where the catalyst is applied to the substrate in a solvent, is preferable that the metal be in the form of a compound which is soluble to the extent of at least 1X10" weight percent of the solvent employed.
  • the transition metal decomposition catalyst is preferably applied to the substrate prior to contact with the aluminum hydride.
  • Such decomposition catalyst may be applied to the substrate directly as a finely divided solid, as a liquid solution or suspension or, where the nature of the catalyst and the substrate permit, deposited by vapor deposition.
  • the substrate is contacted with a sufficient quantity of a relatively dilute solution of the catalyst to Wet the surface of the substrate.
  • the solvent for the catalyst is then removed, e.g., by evaporation, leaving the catalyst substantially uniformly dispersed over the surface to be plated.
  • Catalyst solutions at least about l l0 weight percent in decomposition catalyst, and preferably in concentrations of from about 5X10 to about weight percent of catalyst when applied to the substrate provide sufficient catalyst to achieve plating of aluminum from an aluminum hydride at a significantly lower temperature than is possible where no catalyst is employed. It has been found that uniformity of distribution of the catalyst on the substrate has a significant effect on both the uniformity and thickness of the aluminum plate. It is, therefore, desirable to apply the catalyst to the substrate in a manner which will assure relatively uniform distribution.
  • Suitable wetting agents include, for example, stearates such as sodium or aluminum stearate or aluminum alkoxides such as aluminum isopropoxide.
  • Solvents for the transition metal decomposition catalysts are those normally liquid materials in which the catalyst is soluble to at least the extent of l 10 weight percent, which will not adversely effect the substrate and which will not change the anion of the catalyst sufficiently to render it insoluble.
  • Suitable solvents include non-reactive solvents such as benzene, hexane, and halogenated hydrocarbons, reactive solvents such as alcohols, aldehydes, ketones, mercaptans, carboxylic acids and mineral acids, and coordinating solvents such as ethers, nitriles, amides and amines.
  • transition metal decomposition catalyst By application of the transition metal decomposition catalyst to only selected areas of the substrate, it is possible to form an aluminum plate only on such selected areas. In this manner, ornamental designs, outlines, printed circuits and the like may be produced. Likewise, all or a portion of a selected substrate may be coated or plated with aluminum to enhance the ability of such surface to adhere to other materials. Of particular utility is the aluminum coating of glass, ceramic, metal or polymer surfaces to enhance their bonding to adhesive polymers and copolymers such as the copolymers of ethylene and acrylic acid.
  • the catalyzed substrate surface is contacted with a suitable form of aluminum hydried.
  • a suitable form of aluminum hydried In general, it is desirable to apply the aluminum hydried as a solution or suspension from 0.1 molar to 1.0 molar or more in aluminum hydride which may be applied by dipping, spraying or other suitable means.
  • good results are also achieved by contacting the catalyzed substrate surface with a finely divided solid aluminum hydride.
  • the solvent for the aluminum hydride compound is usually evaporated and the so-treated substrate is then immersed in a hot inert liquid bath containing a dissolved over-coating material.
  • the inert liquid bath can consist of any substance which is a liquid at elevated temperatures, usually at temperatures of from 50 to about 200 C. and which is substantially inert to a aluminum hydride and the particular substrate employed.
  • the bath should be substantially anhydrous i.e., usually containing less than about 20 parts per million of water, due to the sensitivity of most aluminum hydried to moisture.
  • the application of the aluminum hydride compound to the substrate material should be conducted in a substantially anhydrous inert atmosphere for best results.
  • Suitable materials for preparing the bath consist of, for example, naphtha, ethylbutylbenzene,
  • ethylbenzene diphenyl ether, octadecane, xylene and other like materials.
  • Other inert aliphatic, aromatic and ether compounds which are liquid at the indicated temperature range can be employed.
  • the bath should not be prepared from compounds which contain active species such as alcohols, ketones, aldehydes, esters, acids and unsaturated aliphatics since the aluminum plate which develops will be dark, uneven and the substrate will contain unplated areas. It has also been found convenient, although not essential to employ materials which boil in the range of about 100 to about 140 C. Such a bath will allow the application of adequate heat for producing the aluminum plate, yet will evaporate quickly to provide an even overcoat having a minimum of run marks. Higher boiling inert liquids can be removed after the overcoat has been deposited for example, by wiping or draining the coated substrate material.
  • the overcoating material can be any substance which is substantially unreactive with aluminum hydride compounds, which Will provide a clear, flexible and adherent film and which will dissolve or form a liquid dispersion in a heated inert liquid as defined hereinbefore.
  • Coating materials usually consists of an organic material and include for example, insoluble resins such as polyethylene, polypropylene, polyvinylidene fluoride, hexafluoroacetone, polyformaldehyde, polyparaxylene, polyethers, e.g., poly ethylene oxide and polypropylene oxide, copolymers of epoxide and other like materials which dry to a non-tacky finish.
  • the actual overcoating material chosen will depend on the desired toughness and other characteristics of the coating to be formed.
  • the concentration of the overcoating material in the liquid dispersion will depend to some extent on the thickness of the final overcoating desired.
  • the bath should usually be maintained at a temperature of about 50 to about 200 C. A temperature of from about 100 to about 150 C. is usually preferred.
  • the actual deposition temperature of aluminum hydried compounds catalyzed by the transition metal catalysts defined herein will vary depending on the particular aluminum hydride employed, upon the catalyst used and to some extent, upon the catalyst concentration. ISuch deposition temperatures will, however, be substantially lower than those required where no catalyst is present.
  • the present process can be run as a continuous opera tion for the coating of various shaped objects such as films, webs, paper and the like. Also it may be employed to coat various other objects such as whisker materials, beads, powders, various irregularly shaped forms of reflectors for lights, piping and the like.
  • EXAMPLE 1 A sample of a Mylar brand polyester film was first coated with a metal catalyst consisting of TiCL; dissolved in an inert solvent consisting of ethyl ether and the solvent evaporated. Next an AlH solution consisting of 0.25 molar AlH in diethyl ether was applied to the sample and the solvent again evaporated.
  • the solvent bath was heated to about 130 C., and the sample film was submerged in the bath for about 5 seconds, whereupon an aluminum plate formed on the film.
  • the sample was removed from the bath and the xylene allowed to evaporate from the surface thereof.
  • a polystyrene overcoat was deposited onto the metallic aluminum coating. The overcoat was very adherent, lending a good degree of toughness to the coated film.
  • said aluminum hydride decomposition catalyst comprising a compound selected from the group consisting of compounds of the metals selected from the group consisting of V, Nb, Ta, Ti, Zr and Hf;
  • said decomposition catalyst comprises a member selected from the group consisting of bromide, chloride, oxychloride and oxybromide compounds of the metals selected from the group consisting of V, Nb, Ta, Ti, Zr, and Hf.
  • said solvent consists of a substantially anhydrous material which is a liquid at a temperature of from about 50 to 200 C.
  • said substrate is a shaped object of a material selected from organic polymers, glasses, ceramics, metals and cellulose fibers.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Catalysts (AREA)
  • Paints Or Removers (AREA)
  • Chemically Coating (AREA)
US765636A 1968-10-07 1968-10-07 Aluminum plating process Expired - Lifetime US3563787A (en)

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US76563668A 1968-10-07 1968-10-07

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US (1) US3563787A (enrdf_load_stackoverflow)
BE (1) BE739931A (enrdf_load_stackoverflow)
DE (1) DE1949683A1 (enrdf_load_stackoverflow)
FR (1) FR2020025A1 (enrdf_load_stackoverflow)
GB (1) GB1258290A (enrdf_load_stackoverflow)
NL (1) NL6912682A (enrdf_load_stackoverflow)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4262037A (en) * 1976-04-05 1981-04-14 Hitachi, Ltd. Method of producing ferromagnetic metal powder
US4923717A (en) * 1989-03-17 1990-05-08 Regents Of The University Of Minnesota Process for the chemical vapor deposition of aluminum
US5191099A (en) * 1991-09-05 1993-03-02 Regents Of The University Of Minnesota Chemical vapor deposition of aluminum films using dimethylethylamine alane

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2635798C3 (de) * 1976-08-09 1980-10-16 Siemens Ag, 1000 Berlin Und 8000 Muenchen Verfahren zum stromlosen katalytischen Abscheiden von Aluminium, Katalysierbad und Aluminierbad

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4262037A (en) * 1976-04-05 1981-04-14 Hitachi, Ltd. Method of producing ferromagnetic metal powder
US4923717A (en) * 1989-03-17 1990-05-08 Regents Of The University Of Minnesota Process for the chemical vapor deposition of aluminum
WO1990011387A1 (en) * 1989-03-17 1990-10-04 Regents Of The University Of Minnesota Process for chemical vapor deposition of aluminum
US5191099A (en) * 1991-09-05 1993-03-02 Regents Of The University Of Minnesota Chemical vapor deposition of aluminum films using dimethylethylamine alane

Also Published As

Publication number Publication date
FR2020025A1 (enrdf_load_stackoverflow) 1970-07-10
NL6912682A (enrdf_load_stackoverflow) 1970-04-09
BE739931A (enrdf_load_stackoverflow) 1970-04-07
GB1258290A (enrdf_load_stackoverflow) 1971-12-30
DE1949683A1 (de) 1970-04-30

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