US3464844A - Aluminum plating of surfaces - Google Patents
Aluminum plating of surfaces Download PDFInfo
- Publication number
- US3464844A US3464844A US619947A US3464844DA US3464844A US 3464844 A US3464844 A US 3464844A US 619947 A US619947 A US 619947A US 3464844D A US3464844D A US 3464844DA US 3464844 A US3464844 A US 3464844A
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- US
- United States
- Prior art keywords
- aluminum
- temperature
- substrate
- coating
- alkyl
- Prior art date
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- Expired - Lifetime
Links
- 229910052782 aluminium Inorganic materials 0.000 title description 69
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title description 29
- 238000007747 plating Methods 0.000 title description 16
- 235000010210 aluminium Nutrition 0.000 description 69
- 239000000758 substrate Substances 0.000 description 34
- 238000000034 method Methods 0.000 description 31
- 238000000576 coating method Methods 0.000 description 27
- 238000000354 decomposition reaction Methods 0.000 description 22
- 239000011248 coating agent Substances 0.000 description 21
- -1 diphenyl alkanes Chemical class 0.000 description 20
- 238000009835 boiling Methods 0.000 description 17
- 239000002904 solvent Substances 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 229930195733 hydrocarbon Natural products 0.000 description 12
- 150000002430 hydrocarbons Chemical class 0.000 description 12
- 239000004215 Carbon black (E152) Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 238000010438 heat treatment Methods 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000012298 atmosphere Substances 0.000 description 5
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- HJXBDPDUCXORKZ-UHFFFAOYSA-N diethylalumane Chemical compound CC[AlH]CC HJXBDPDUCXORKZ-UHFFFAOYSA-N 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000004678 hydrides Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- AZWXAPCAJCYGIA-UHFFFAOYSA-N bis(2-methylpropyl)alumane Chemical compound CC(C)C[AlH]CC(C)C AZWXAPCAJCYGIA-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- VTZJFPSWNQFPCQ-UHFFFAOYSA-N dibutylaluminum Chemical compound CCCC[Al]CCCC VTZJFPSWNQFPCQ-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 231100000989 no adverse effect Toxicity 0.000 description 2
- UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 2
- CNWZYDSEVLFSMS-UHFFFAOYSA-N tripropylalumane Chemical compound CCC[Al](CCC)CCC CNWZYDSEVLFSMS-UHFFFAOYSA-N 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- URDDUZADOOBXOJ-UHFFFAOYSA-N 1,2-di(tetradecyl)benzene Chemical compound CCCCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCCCC URDDUZADOOBXOJ-UHFFFAOYSA-N 0.000 description 1
- PODLNLIJRFYBJK-UHFFFAOYSA-N 1,2-di(tridecyl)benzene Chemical compound CCCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCCC PODLNLIJRFYBJK-UHFFFAOYSA-N 0.000 description 1
- DZUCNDRXUNGSMM-UHFFFAOYSA-N 1,2-di(undecyl)benzene Chemical compound CCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCC DZUCNDRXUNGSMM-UHFFFAOYSA-N 0.000 description 1
- FVEVOEHPSHPIOH-UHFFFAOYSA-N 1,2-didecylbenzene Chemical compound CCCCCCCCCCC1=CC=CC=C1CCCCCCCCCC FVEVOEHPSHPIOH-UHFFFAOYSA-N 0.000 description 1
- WJECKFZULSWXPN-UHFFFAOYSA-N 1,2-didodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCC WJECKFZULSWXPN-UHFFFAOYSA-N 0.000 description 1
- HSTCJLDQVIIDKF-UHFFFAOYSA-N 1-phenyldecylbenzene Chemical compound C=1C=CC=CC=1C(CCCCCCCCC)C1=CC=CC=C1 HSTCJLDQVIIDKF-UHFFFAOYSA-N 0.000 description 1
- MPUACKZXJBPMHK-UHFFFAOYSA-N 1-phenyldodecylbenzene Chemical compound C=1C=CC=CC=1C(CCCCCCCCCCC)C1=CC=CC=C1 MPUACKZXJBPMHK-UHFFFAOYSA-N 0.000 description 1
- RHISRDQWNQEBBY-UHFFFAOYSA-N 1-phenyltetradecylbenzene Chemical compound C=1C=CC=CC=1C(CCCCCCCCCCCCC)C1=CC=CC=C1 RHISRDQWNQEBBY-UHFFFAOYSA-N 0.000 description 1
- REGVVWIVILJTIW-UHFFFAOYSA-N 1-phenyltridecylbenzene Chemical compound C=1C=CC=CC=1C(CCCCCCCCCCCC)C1=CC=CC=C1 REGVVWIVILJTIW-UHFFFAOYSA-N 0.000 description 1
- HUMMQDLHLVLHCE-UHFFFAOYSA-N 1-phenylundecylbenzene Chemical compound C=1C=CC=CC=1C(CCCCCCCCCC)C1=CC=CC=C1 HUMMQDLHLVLHCE-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000005234 alkyl aluminium group Chemical group 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- CDHICTNQMQYRSM-UHFFFAOYSA-N di(propan-2-yl)alumane Chemical compound CC(C)[AlH]C(C)C CDHICTNQMQYRSM-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical group C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
Definitions
- This invention relates to a method of coating a surface with aluminum. In one of its more specific aspects this invention relates to a method of protecting a surface against oxidation prior to contacting said surface With a plating batch. In another aspect this invention relates to liquid bath plating with aluminum.
- a heat decomposable aluminum compound in a liquid or solid solution or dispersion said liquid or solid being stable and having a boiling point above the decomposition temperature of the aluminum compound, is put into contact with a substrate heated to a temperature above the decomposition temperature causing formation of aluminum on the .substrate.
- Other materials can be present, for example reducers or oxidizers.
- the substrate can be of any desirable material so long as said substrate can be heated to a temperature above the decomposition temperature of the aluminum compound.
- the deposited aluminum film can be anodized by conventional procedures.
- Such substrates are first cleaned of surface oxidation material and are heated to a temperature above the decomposition temperature of the aluminum compound and subsequently coated by the solution. It is necessary to heat the substrate in a dry box which has been flushed with a inert gas.
- these extremely hot surfaces are very active and are readily oxidized by even trace amounts of oxygen.
- the surface to be coated should be prefectly clean and free of any oxides.
- This cleaning can be mechanical such as by abrasion with steel wool, sandblasting, sandpaper, and the like.
- the cleaning can also be by chemical means such as ammonia solution of citric acid, dilute hydrochloric acid, dilute phosphoric acid and the like.
- the chemical cleaning agent can be washed off with water and dried with suitable drying agents such as acetone or methanol.
- the solvents suitable in the practice of this invention are fully disclosed by Berger and the copending application supra. They include alkanes, aromatics and paraflins, ethers and substituted compounds of this type. These include n-dodecane, 1,2,3,4 tetramethylbenzene, tetralin, naphthalene, diphenyl, anthracene, parafiin distillate, toluene, ethyl benzene, xylene, kerosene and the like. However, hydrocarbons are generally preferred.
- Suitable bath temperature will depend upon the solvent used and the aluminum compound. The temperature should be below the boiling point of the solvent and also below the decomposition temperature of the aluminum compound. In general, the solution temperature will be between 50 C. and about C. We prefer a solvent that has a boiling temperature below that of the decomposition temperature of the aluminum compound and prefer to maintain the bath at a temperature between 50 and 150 C.
- any aluminum-containing organic compound capable of decomposing under heat to liberate aluminum and which can be dissolved or suspended in a solvent medium, can be utilized to product an aluminum film on a substrate in the practice of this invention.
- the aluminum alkyls are generally preferred. Examples of such aluminum compounds include aluminum trimethyl, aluminum tri ethyl, tripropyl aluminum, aluminum tributyl, aluminum tri-isobutyl, aluminum tri-isopentyl, aluminum tri-isooctyl and aluminum tridodecyl. Also operable are substituted alkyls, preferably wherein the substituent is a saturated aliphatic radical.
- monoand dialkyl aluminums can be used. Examples include ethyl aluminum dihydride and diethylaluminum hydride, di-isopropylaluminum hydride, aluminum dibutyl hydride, aluminum di-isobutyl hydride and the like.
- the preferred material is a trialkylaluminum or a dialkylaluminum hydride wherein each alkyl radical contains one to four carbon atoms, and, in particular, we prefer aluminum triethyl and diethyl aluminum hydride.
- the aluminum alkyl in solvent can vary from to 90 weight percent, and most generally will be present in the range 30 to 70 weight percent.
- solvent medium can be employed to cause modification of the physical and chemical properties of the film deposited.
- materials as wetting agents to promote adhesion, oxidizing and reducing compounds can be employed.
- the precoating of the substrate by the practice of this invention protects the substrate from such compounds and permits it to modify only the coating.
- the substrate treatment coating material of thi invention is a heavy hydrocarbon having a boiling point in excess of the decomposition temperature of the aluminum alkyl.
- They include the well known mineral oils and waxes, diphenyl alkanes which contain two phenyl groups distributed randomly along a normal paraffin, preferably of a C to C backbone and dialkylbenzenes, preferably with each alkyl containing 10 to 14 carbon atoms and mainly meta and para isomers prepared by alkylation of benzene with chloroalkanes.
- These materials are obtained from petroleu m, generally by fractionation in various temperature range cuts and have no fixed chemical makeup. Such compounds generally have a boiling range from 250 to 350C.
- the coating material would be completely evaporated under the temperature conditions of the furnace (400-550" C.). At these": temperatures one would expect to find decomposition of the mineral oil and fouling of the substrate; however, it has been found that no decomposition occurs, and the substrate is substantially free of oxides.
- the resulting aluminum plate i far superior to plate prepared under identical conditions except for the coating.
- suitable coating materials include, but are not limited to, mineral oils, paraflin waxes, diphenyl decane, diphenyl undecane, diphenyl dodecane, diphenyl tridecane, diphenyl tetradecane, didecyl benzene, diundecyl benzene, didodecyl benzene, ditridecyl benzene and ditetradecylbenzene.
- the aluminum plate produced by the process of this invention is flexible, the coated material, e.g. iron strip, can be bent and twisted repeatedly without breakingthe coating-The coating is more resistant to tape-pull-test than are other coatings. This test comprises pressing tape on the coating and pulling it off. Bright, shiny, lustrous aluminum coatings are obtained.
- the substrates to be treated by the method of this invention are ones that can be oxidized. In general this includes metal substrates and particularly metal strips. Most frequently, the metal to be treated will be in iron alloy such as mild steel. However, other metals such as copper strips or articles can be advantageously treated by the method of this invention.
- the plating can be done by any suitable method.
- the plating bath (aluminum compound in solvent) will be maintained at a temperature below the boiling point of the solvent and below the decomposition temperature of the aluminum compound and generally above ambient temperature, however, the initial bath temperature can be at room temperature.
- the bath temperature will be determined largely by the nature of the solvent, the aluminum compound and the temperature differential of bath and substrate desired. As a general rule a temperature in the range 50 to C. will be employed; however, any temperature up to the boiling point of the solvent can be employed.
- the substrate after cleaning and removal of oxides will be coated with the heavy hydrocarbon and then heated to a temperature above the decomposition temperature of the aluminum compound.
- This temperature will, of course, depend upon the particular aluminum compound and will be sufficiently high to offset the cooling effect of the bath.
- the temperature ordinarily employed ranges from about 400 to 550 C.
- the coating is tough and resist flexing, however, such coatings are unusually thin.
- Several treatments can improve the thickness.
- the temperature exceeds about 550 C., the coatings tend to flake or crack on flexing. Where these limitations are not important, we can use temperatures from about 300' to 1000 C.
- the article to be plated is then contacted by the plating bath while at this high heat.
- the contacting can be done by dipping the article in the bath, passing it through the bath, spraying with the bath or any other suitable means. Since frequently these solvents are flammable, it is preferred that the bath be in an oxygen-free atmosphere. It is also within the scope of the invention to heat the substrate in the oxygen-free atmosphere. However, with the coating treatment of this invention, the operation can be performed in the natural atmosphere and in small amounts of oxygen in the oxygen-free atmosphere can be tolerated. That is, the system would not require the taking of extensive precautions to exclude all oxygen. However, even in oxygen-free atmosphere, more uniform and stronger coatings have been obtained than when the coating was not applied. When the coating material has sutficiently high boiling point, the coating material can be held at the desired temperature and the article heated in the coating bath and then contacted with the plating bath.
- a 50% solution of diethylalminum hydride in a hydrocarbon wash oil was heated in an oil bath to about 150 C.
- Two clean mild steel coupons (1 x 3 x 0.03 inch) were coated with a thin film of mineral oil. They were then placed in a muffle furnace and heated to 500 C. The coupons were then removed from the furnace and dipped into the plating bath, i.e. the alkyl aluminum solution.
- the plated coupons were repeatedly bent and twisted with no adverse effect.
- the plating was uniform but failed when bent or twisted.
- a process for plating aluminum on a metal substrate which comprises preparing a solution of an aluminum capable of decomposing under heat in an organic solvent having a boiling point below the decomposition temperature of the aluminum alkyl, coating said substrate with a heavy hydrocarbon having a boiling point above the decomposition temperature of said aluminum alkyl, heating the coated substrate to a temperature above the boiling point of said heavy hydrocarbon and contacting the heated substrate with said solution.
- a process for plating aluminum on a metal substrate comprising preparing a solution of an aluminum alkyl in a hydrocarbon solvent having a boiling point below the decomposition temperature of said aluminum alkyl, said aluminum alkyl being present in the range of 10 to weight percent; coating said substrate with a film of a heavy hydrocarbon having a boiling point above the decomposition temperature of said aluminum alkyl, heating the coated substrate to a temperature above the decomposition temperature of the aluminum alkyl and above the boiling point of said heavy hydrocarbon; and thereafter contacting the hot substrate with said solution.
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- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemically Coating (AREA)
Description
United States Patent O US. 'Cl. 11746 18 Claims ABSTRACT OF THE DISCLOSURE Where an object is to be plated with aluminum alkyl decomposition in liquid phase aluminum by heating said object to a temperature above the decomposition temperature of the aluminum alkyl and thereafter contacting the heated article with a solution of aluminum alkyl, the article to be plated is first coated with a heavy hydrocarbon to protect the article from oxidation.
CROSS REFERENCE This is a continuation-in-part of my application having Ser. No. 444,392, filed Mar. 31, 1965, now abandoned.
FIELD OF INVENTION This invention relates to a method of coating a surface with aluminum. In one of its more specific aspects this invention relates to a method of protecting a surface against oxidation prior to contacting said surface With a plating batch. In another aspect this invention relates to liquid bath plating with aluminum.
BACKGROUND In the earlier filed application, I disclosed coating the article to be treated with high boiling waxes and mineral oils. Subsequent to-filing the parent application, I have found that certain diphenyl alkanes and certain dialkyl benzenes are especially suited as coating materials. While I was not restricted to separate heating in the earlier application, I wish to specifically disclosed heating the article to be plated in the coating oil in this application.
Various systems have been used to coat an oxidizable surface such as mild steel with aluminum. Cladding techniques have been employed wherein an aluminum sheet is bonded to the desired substrate or surface by extensive surface treatment of the article followed by a combination of heat and pressure. High operating pressures are necessary, thus limiting the type of articles which could be covered. Also, serious corrosion and operating problems are encountered.
The various well known vacuum techniques produce quite thin films and are subject to low production levels, batch operations and severe size limitations.
The heat decomposition of aluminum compounds is recorded in the literature. Aluminum hydride has been decomposed into aluminum and hydrogen. Vapor phase plating by decomposition of such aluminum compounds has been disclosed.
With gasor vapor phase plating, a number of practical problems are encountered. The systems must be tightly sealed against atmospheric contamination, constant pressure conditions maintained and gas flow rates controlled with narrow limits. Also, many problems exist in vaporizing decomposable materials, and in almost all cases a carrier gas must be provided to give direction to the fiow of the decomposable gas. All additives to the gas stream, such as modifiers, must also be volatile at the operating temperature and the rates of addition care- 3,464,844 Patented Sept. 2, 1969 sive process equipment (see Berger, US. Patent 3,041,-
Berger, in the US. patent supra, makes a major break through in aluminum plating by use of solution plating. In his system a heat decomposable aluminum compound in a liquid or solid solution or dispersion, said liquid or solid being stable and having a boiling point above the decomposition temperature of the aluminum compound, is put into contact with a substrate heated to a temperature above the decomposition temperature causing formation of aluminum on the .substrate. Other materials can be present, for example reducers or oxidizers. The substrate can be of any desirable material so long as said substrate can be heated to a temperature above the decomposition temperature of the aluminum compound. The deposited aluminum film can be anodized by conventional procedures.
In the process of Williams and Kostas in copending application filed Mar. 31, 1965, and having Ser. No. 444,- 431, it is disclosed that the Berger process has certain disadvantages such as excessive smoking, splattering and decomposition of the aluminum compound in the solvent. In this copending application it is shown that much superior coatings are obtained if the solvent for the aluminum compound has a boiling point below the decomposition temperature of the aluminum compound.
It is frequently desired to plate an oxidizable substrate. Such substrates are first cleaned of surface oxidation material and are heated to a temperature above the decomposition temperature of the aluminum compound and subsequently coated by the solution. It is necessary to heat the substrate in a dry box which has been flushed with a inert gas. However, these extremely hot surfaces are very active and are readily oxidized by even trace amounts of oxygen.
It is, therefore, an object of this invention to provide a method of protecting a substrate to be plated at high temperatures against oxidation at said high temperatures. Other objects and advantages of this invention will be apparent from the specification and the claims.
These and other objects of the invention are obtained by coating a substrate prior to heating With a high boiling liquid hydrocarbon.
The surface to be coated should be prefectly clean and free of any oxides. This cleaning can be mechanical such as by abrasion with steel wool, sandblasting, sandpaper, and the like. The cleaning can also be by chemical means such as ammonia solution of citric acid, dilute hydrochloric acid, dilute phosphoric acid and the like. The chemical cleaning agent can be washed off with water and dried with suitable drying agents such as acetone or methanol.
The solvents suitable in the practice of this invention are fully disclosed by Berger and the copending application supra. They include alkanes, aromatics and paraflins, ethers and substituted compounds of this type. These include n-dodecane, 1,2,3,4 tetramethylbenzene, tetralin, naphthalene, diphenyl, anthracene, parafiin distillate, toluene, ethyl benzene, xylene, kerosene and the like. However, hydrocarbons are generally preferred. Suitable bath temperature will depend upon the solvent used and the aluminum compound. The temperature should be below the boiling point of the solvent and also below the decomposition temperature of the aluminum compound. In general, the solution temperature will be between 50 C. and about C. We prefer a solvent that has a boiling temperature below that of the decomposition temperature of the aluminum compound and prefer to maintain the bath at a temperature between 50 and 150 C.
Any aluminum-containing organic compound, capable of decomposing under heat to liberate aluminum and which can be dissolved or suspended in a solvent medium, can be utilized to product an aluminum film on a substrate in the practice of this invention. As a practical matter, due to cost, availability, safety, and the temperature to which the Substrate may be heated, the aluminum alkyls are generally preferred. Examples of such aluminum compounds include aluminum trimethyl, aluminum tri ethyl, tripropyl aluminum, aluminum tributyl, aluminum tri-isobutyl, aluminum tri-isopentyl, aluminum tri-isooctyl and aluminum tridodecyl. Also operable are substituted alkyls, preferably wherein the substituent is a saturated aliphatic radical. Substituents tending to react with the newly deposited aluminum coating would ordinarily be avoided. Also monoand dialkyl aluminums can be used. Examples include ethyl aluminum dihydride and diethylaluminum hydride, di-isopropylaluminum hydride, aluminum dibutyl hydride, aluminum di-isobutyl hydride and the like. In general, the preferred material is a trialkylaluminum or a dialkylaluminum hydride wherein each alkyl radical contains one to four carbon atoms, and, in particular, we prefer aluminum triethyl and diethyl aluminum hydride.
The aluminum alkyl in solvent can vary from to 90 weight percent, and most generally will be present in the range 30 to 70 weight percent.
As has been indicated, the use of various minor components in solvent medium can be employed to cause modification of the physical and chemical properties of the film deposited. Such materials as wetting agents to promote adhesion, oxidizing and reducing compounds can be employed. The precoating of the substrate by the practice of this invention protects the substrate from such compounds and permits it to modify only the coating.
The substrate treatment coating material of thi invention is a heavy hydrocarbon having a boiling point in excess of the decomposition temperature of the aluminum alkyl. They include the well known mineral oils and waxes, diphenyl alkanes which contain two phenyl groups distributed randomly along a normal paraffin, preferably of a C to C backbone and dialkylbenzenes, preferably with each alkyl containing 10 to 14 carbon atoms and mainly meta and para isomers prepared by alkylation of benzene with chloroalkanes. These materials are obtained from petroleu m, generally by fractionation in various temperature range cuts and have no fixed chemical makeup. Such compounds generally have a boiling range from 250 to 350C. It would be expected, therefore, that the coating material would be completely evaporated under the temperature conditions of the furnace (400-550" C.). At these": temperatures one would expect to find decomposition of the mineral oil and fouling of the substrate; however, it has been found that no decomposition occurs, and the substrate is substantially free of oxides. The resulting aluminum plate i far superior to plate prepared under identical conditions except for the coating. Examples of suitable coating materials then include, but are not limited to, mineral oils, paraflin waxes, diphenyl decane, diphenyl undecane, diphenyl dodecane, diphenyl tridecane, diphenyl tetradecane, didecyl benzene, diundecyl benzene, didodecyl benzene, ditridecyl benzene and ditetradecylbenzene.
The aluminum plate produced by the process of this invention is flexible, the coated material, e.g. iron strip, can be bent and twisted repeatedly without breakingthe coating-The coating is more resistant to tape-pull-test than are other coatings. This test comprises pressing tape on the coating and pulling it off. Bright, shiny, lustrous aluminum coatings are obtained.
The substrates to be treated by the method of this invention are ones that can be oxidized. In general this includes metal substrates and particularly metal strips. Most frequently, the metal to be treated will be in iron alloy such as mild steel. However, other metals such as copper strips or articles can be advantageously treated by the method of this invention.
The plating can be done by any suitable method. The plating bath (aluminum compound in solvent) will be maintained at a temperature below the boiling point of the solvent and below the decomposition temperature of the aluminum compound and generally above ambient temperature, however, the initial bath temperature can be at room temperature. The bath temperature will be determined largely by the nature of the solvent, the aluminum compound and the temperature differential of bath and substrate desired. As a general rule a temperature in the range 50 to C. will be employed; however, any temperature up to the boiling point of the solvent can be employed.
The substrate, after cleaning and removal of oxides will be coated with the heavy hydrocarbon and then heated to a temperature above the decomposition temperature of the aluminum compound. This temperature will, of course, depend upon the particular aluminum compound and will be sufficiently high to offset the cooling effect of the bath. The temperature ordinarily employed ranges from about 400 to 550 C. When the substrate is heated to much below 400 C., the coating is tough and resist flexing, however, such coatings are unusually thin. Several treatments can improve the thickness. When the temperature exceeds about 550 C., the coatings tend to flake or crack on flexing. Where these limitations are not important, we can use temperatures from about 300' to 1000 C.
The article to be plated is then contacted by the plating bath while at this high heat. The contacting can be done by dipping the article in the bath, passing it through the bath, spraying with the bath or any other suitable means. Since frequently these solvents are flammable, it is preferred that the bath be in an oxygen-free atmosphere. It is also within the scope of the invention to heat the substrate in the oxygen-free atmosphere. However, with the coating treatment of this invention, the operation can be performed in the natural atmosphere and in small amounts of oxygen in the oxygen-free atmosphere can be tolerated. That is, the system would not require the taking of extensive precautions to exclude all oxygen. However, even in oxygen-free atmosphere, more uniform and stronger coatings have been obtained than when the coating was not applied. When the coating material has sutficiently high boiling point, the coating material can be held at the desired temperature and the article heated in the coating bath and then contacted with the plating bath.
To further illustrate the invention, the following examples are given. It is to be understood that these serve to illustrate the invention and are not to be considered limiting.
EXAMPLE I Several runs were made wherein thin strips of mild steel were plated. The plating operation was carried out in a nitrogen purged dry box. The heating furnace was also in the dry box.
A 50% solution of diethylalminum hydride in a hydrocarbon wash oil was heated in an oil bath to about 150 C. Two clean mild steel coupons (1 x 3 x 0.03 inch) were coated with a thin film of mineral oil. They were then placed in a muffle furnace and heated to 500 C. The coupons were then removed from the furnace and dipped into the plating bath, i.e. the alkyl aluminum solution.
The plated coupons were repeatedly bent and twisted with no adverse effect.
EXAMPLE II The above run was repeated except the two coupons were coated by dipping into a 20% solution of mineral oil in toluene.
Again the strips showed no adverse effect from twisting and bending.
EXAMPLE III This run was the same as run 1 except the coupons were not first coated.
The plating was uniform but failed when bent or twisted.
EXAMPLE IV Oven Conditions Flex Time Temp., 0. Tape pull test test Run:
1 1min... 500 Good Good. 2 1min 500 Having thus described the invention, what is claimed 1. A process for plating aluminum on a metal substrate which comprises preparing a solution of an aluminum capable of decomposing under heat in an organic solvent having a boiling point below the decomposition temperature of the aluminum alkyl, coating said substrate with a heavy hydrocarbon having a boiling point above the decomposition temperature of said aluminum alkyl, heating the coated substrate to a temperature above the boiling point of said heavy hydrocarbon and contacting the heated substrate with said solution.
2. The process of claim 1 wherein said heavy hydrocarbon is a mineral oil.
3. The process of claim 2 wherein the aluminum alkyl is diethylaluminum hydride.
4. The process of claim 2 wherein the aluminum alkyl is triethylaluminum.
5. The process of claim 2 wherein the aluminum alkyl is tri-isobutylaluminum.
6. The process of claim 2 wherein the aluminum alkyl is di-isobutylaluminum hydride.
7. The process of claim 2 wherein the aluminum alkyl is triethylaluminum.
8. The process of claim 2 wherein the aluminum alkyl is di-n-butylaluminum hydride.
9. A process for plating aluminum on a metal substrate comprising preparing a solution of an aluminum alkyl in a hydrocarbon solvent having a boiling point below the decomposition temperature of said aluminum alkyl, said aluminum alkyl being present in the range of 10 to weight percent; coating said substrate with a film of a heavy hydrocarbon having a boiling point above the decomposition temperature of said aluminum alkyl, heating the coated substrate to a temperature above the decomposition temperature of the aluminum alkyl and above the boiling point of said heavy hydrocarbon; and thereafter contacting the hot substrate with said solution.
10. The process of claim 9 wherein the substrate is heated to a temperature in the range 300-1000 C.
11. The process of claim 4 wherein the substrate is heated to a temperature within the range 450550 C.
12. The process of claim 10 wherein the aluminum alkyl is diethylaluminum hydride.
13. The process of claim 12 wherein said substrate is contacted by spraying.
14. The process of claim 10 wherein the aluminum alkyl is triethylaluminum.
15. The process of claim 10 wherein the aluminum alkyl is tri-isobutylaluminum.
16. The process of claim 10 wherein the aluminum alkyl is di-isobutylaluminum hydride.
17. The process of claim 10 wherein the aluminum alkyl is tripropylaluminum.
18. The process of claim 10 wherein the aluminum alkyl is di-n-butylaluminum hydride.
References Cited UNITED STATES PATENTS 2,523,461 9/1950 Young et a1. 11747 2,619,433 12/1952 Davis et al 117-107.2 X 2,698,811 1/1955 Legg 11746 3,041,197 6/1962 Berger 11747 3,075,858 1/1963 Breining 117107 3,155,532 11/1964 Basile 117 47 3,198,167 8/1965 Bakish et a1. 117-l07.2 X 3,305,386 2/1967 Hafiver et al. 117107.2 X
ALFRED L. LEAVITT, Primary Examiner A. GOLIAN, Assistant Examiner US. Cl. X.R. 1l7-50, 105,
iii/ 1f UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent 3, 464,544 Dated September 2, 1969 Inventofls) Billv J. Williams It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 1, line +3, "disclosed" should be --disclose-.-. Column 2, line 55, "a" should be --an--. Column 3, line 4, "product" should be --produce--. Column 5, line 13, before "alkyls" insert --aluminuJn--. Claim 1, line 3, before "capable" insert --alkyl--. Claim 7, line 2, "triethylaluminum" should be --tripropylaluminum--.
SIGNED AND SEALED MAY 5 1970 (SEAL) Attest:
d d M. Fletcher, 11-
mum: E. *saaumm, m. Attefl g Comisaioner o1 Patents
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61994767A | 1967-03-02 | 1967-03-02 |
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| Publication Number | Publication Date |
|---|---|
| US3464844A true US3464844A (en) | 1969-09-02 |
Family
ID=24483959
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US619947A Expired - Lifetime US3464844A (en) | 1967-03-02 | 1967-03-02 | Aluminum plating of surfaces |
Country Status (1)
| Country | Link |
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| US (1) | US3464844A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3772058A (en) * | 1969-10-01 | 1973-11-13 | Texas Instruments Inc | Formation of refractory coatings on steel without loss of temper of steel |
| US3836385A (en) * | 1972-02-02 | 1974-09-17 | Dow Chemical Co | Cyclic sulfonium zwitterion-titanium catalysts for aluminum plating process |
| US20050064211A1 (en) * | 2003-09-19 | 2005-03-24 | Deavenport Dennis Leon | Metallization of substrate(s) by a liquid/vapor deposition process |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US2523461A (en) * | 1946-03-15 | 1950-09-26 | John T Young | Plating with metal carbonyl |
| US2619433A (en) * | 1949-07-14 | 1952-11-25 | Ohio Commw Eng Co | Method of gas plating |
| US2698811A (en) * | 1952-03-03 | 1955-01-04 | Kaiser Aluminium Chem Corp | Articles and process of fabricating |
| US3041197A (en) * | 1959-06-01 | 1962-06-26 | Berger Carl | Coating surfaces with aluminum |
| US3075858A (en) * | 1958-01-21 | 1963-01-29 | Union Carbide Corp | Deposition of composite coatings by vapor phase plating method |
| US3155532A (en) * | 1960-11-10 | 1964-11-03 | Union Carbide Corp | Metal plating process |
| US3198167A (en) * | 1961-03-10 | 1965-08-03 | Alloyd Corp | Vapor deposition device |
| US3305386A (en) * | 1955-10-05 | 1967-02-21 | Union Carbide Corp | Metal plating process utilizing bis (arene) metal compounds |
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Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2523461A (en) * | 1946-03-15 | 1950-09-26 | John T Young | Plating with metal carbonyl |
| US2619433A (en) * | 1949-07-14 | 1952-11-25 | Ohio Commw Eng Co | Method of gas plating |
| US2698811A (en) * | 1952-03-03 | 1955-01-04 | Kaiser Aluminium Chem Corp | Articles and process of fabricating |
| US3305386A (en) * | 1955-10-05 | 1967-02-21 | Union Carbide Corp | Metal plating process utilizing bis (arene) metal compounds |
| US3075858A (en) * | 1958-01-21 | 1963-01-29 | Union Carbide Corp | Deposition of composite coatings by vapor phase plating method |
| US3041197A (en) * | 1959-06-01 | 1962-06-26 | Berger Carl | Coating surfaces with aluminum |
| US3155532A (en) * | 1960-11-10 | 1964-11-03 | Union Carbide Corp | Metal plating process |
| US3198167A (en) * | 1961-03-10 | 1965-08-03 | Alloyd Corp | Vapor deposition device |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3772058A (en) * | 1969-10-01 | 1973-11-13 | Texas Instruments Inc | Formation of refractory coatings on steel without loss of temper of steel |
| US3836385A (en) * | 1972-02-02 | 1974-09-17 | Dow Chemical Co | Cyclic sulfonium zwitterion-titanium catalysts for aluminum plating process |
| US20050064211A1 (en) * | 2003-09-19 | 2005-03-24 | Deavenport Dennis Leon | Metallization of substrate(s) by a liquid/vapor deposition process |
| US7387815B2 (en) | 2003-09-19 | 2008-06-17 | Akzo Nobel N.V. | Metallization of substrate(s) by a liquid/vapor deposition process |
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