GB708488A - Improvements in or relating to aluminium and/or aluminium oxide coated metals - Google Patents
Improvements in or relating to aluminium and/or aluminium oxide coated metalsInfo
- Publication number
- GB708488A GB708488A GB1432952A GB1432952A GB708488A GB 708488 A GB708488 A GB 708488A GB 1432952 A GB1432952 A GB 1432952A GB 1432952 A GB1432952 A GB 1432952A GB 708488 A GB708488 A GB 708488A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aluminium
- prepared
- cresol
- alcoholates
- hydric
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
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
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/02—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using non-aqueous solutions
Landscapes
- Chemical & Material 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)
- Lubricants (AREA)
Abstract
Aluminium alcoholates may be prepared from methanol, ethanol, isopropanol, butanol, tert.-butanol, hexanol, isohexanol, heptanol, tert.-octanol, 2-ethyl-hexanol, 2 : 5-dimethyl heptanol, dodecanol, tetradecanol, penta-decanol, octadecanol, cyclohexanol, methylcyclohexanol, furfuryl alcohol, benzyl alcohol, ethylene glycol, diethylene glycol, propylene glycol, glycerol, sorbitol and mannitol. Aluminium phenates may be prepared from phenol, o-cresol, m-cresol, p-cresol, commercial cresol mixtures, the xylenols a - and b -naphthols, resorcinol and pyrogallol. Alcoholates may also be prepared from mixtures of alcohols obtained by hydration of mixtures of olefins obtained in cracking petroleum fractions, or by reaction of such olefins with carbon monoxide and hydrogen in the Oxo process. Alcoholates may be prepared from aluminium powder or turnings heated under reflux with excess of the alcohol. Or the calculated amount of alcohol may be used with an inert solvent such as benzene, toluene or xylene. The aluminium may be activated by the addition of iodine or mercuric chloride. The alcoholates (excepting the methoxide) may be purified by distillation under reduced pressure. Aluminium ethoxide may be prepared using aluminium powder, xylene and absolute alcohol with mercuric chloride and iodine. Aluminium phenates may be prepared similarly by reacting aluminium with a phenol in a solvent.ALSO:A process for the protection of aluminium and/or aluminium oxide coated metals comprises applying to the surface thereof a p fluid consisting of, or containing, an aluminium alcoholate or phenate. The alcoholates may be prepared from mono-hydric, di-hydric or poly-hydric alcohols, which may be saturated or unsaturated, aliphatic, cyclic, alicyclic, heterocyclic or aromatic, such as methanol, ethanol, isopropanol, butanol, tert-butanol, hexanol, isohexanol, heptanol, tert.-octanol, 2-ethyl-hexanol, 2 : 5- dimethyl heptanol, dodecanol, tetradecanol, pentadecanol, octadecanol, cyclohexanol, methylcyclohexanol, furfuryl alcohol, benzyl alcohol, ethylene glycol, diethylene glycol, propylene glycol, glycerol, sorbitol, or mannitol. The preferred alcohols are saturated aliphatic alcohols containing not more than 4 carbon atoms. The phenate may be prepared from mono-hydric, dihydric or poly-hydric phenols which may be mono-cyclic or poly-cyclic, such as phenol, o-cresol, m-cresol, pcresol, xylenols alpha and b naphthols, resorcinol or pyrogallol. The alumminium alcoholate may, if sufficiently volatile, be applied as a vapour by vacuum evaporation, or the undiluted liquid compound may be brushed or sprayed on the surface. Preferably the compound is applied in solution in a volatile solvent of low surface tension, such as benzene toluene, xylenes, methanol, ethanol, isopropanol, acetone, methyl ethyl ketone, diethyl ether or di-isopropyl ether. The solution may be brushed or sprayed on. The aluminium compound decomposes in pores in the coating to form aluminium hydroxide or alumina, which acts as a barrier and enhances the protection afforded by the coating.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1432952A GB708488A (en) | 1952-06-06 | 1952-06-06 | Improvements in or relating to aluminium and/or aluminium oxide coated metals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1432952A GB708488A (en) | 1952-06-06 | 1952-06-06 | Improvements in or relating to aluminium and/or aluminium oxide coated metals |
Publications (1)
Publication Number | Publication Date |
---|---|
GB708488A true GB708488A (en) | 1954-05-05 |
Family
ID=10039224
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1432952A Expired GB708488A (en) | 1952-06-06 | 1952-06-06 | Improvements in or relating to aluminium and/or aluminium oxide coated metals |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB708488A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1122171B (en) * | 1955-11-10 | 1962-01-18 | Robert Mueller | Process for the production of electrical capacitors, which consist of an insulation material with thin aluminum layers adhering to it |
DE1206697B (en) * | 1958-06-09 | 1965-12-09 | Union Carbide Corp | Process for applying an aluminum coating to surfaces of objects made of different materials |
DE1235106B (en) * | 1960-02-29 | 1967-02-23 | Union Carbide Corp | Process for the gas plating of aluminum on heated objects |
DE1267054B (en) * | 1958-09-10 | 1968-04-25 | Union Carbide Corp | Gas plating process for the production of aluminum coatings |
DE1267053B (en) * | 1958-09-01 | 1968-04-25 | Union Carbide Corp | Coating of metal objects with magnesium |
-
1952
- 1952-06-06 GB GB1432952A patent/GB708488A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1122171B (en) * | 1955-11-10 | 1962-01-18 | Robert Mueller | Process for the production of electrical capacitors, which consist of an insulation material with thin aluminum layers adhering to it |
DE1206697B (en) * | 1958-06-09 | 1965-12-09 | Union Carbide Corp | Process for applying an aluminum coating to surfaces of objects made of different materials |
DE1267053B (en) * | 1958-09-01 | 1968-04-25 | Union Carbide Corp | Coating of metal objects with magnesium |
DE1267054B (en) * | 1958-09-10 | 1968-04-25 | Union Carbide Corp | Gas plating process for the production of aluminum coatings |
DE1235106B (en) * | 1960-02-29 | 1967-02-23 | Union Carbide Corp | Process for the gas plating of aluminum on heated objects |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Johnson et al. | Sodium borohydride reduction of conjugated aldehydes and ketones | |
US2448942A (en) | Alkylation of phenolic compounds | |
McKillop et al. | Thallium in organic synthesis. XXXIII. One-step synthesis of methyl arylacetates from acetophenones using thallium (III) nitrate (TTN) | |
Kuwajima et al. | Fluoride catalyzed reaction of silylacetylenes with carbonyl compounds | |
GB708488A (en) | Improvements in or relating to aluminium and/or aluminium oxide coated metals | |
SEARLES Jr et al. | Oxetanes. IX. Structural and Solvent Effects in the Reaction of γ-Bromoalcohols with Base1, 2 | |
Lorette et al. | The cracking and rearrangement of diallyl ketals to α-allyl ketones | |
Royals et al. | Hydroxymethylene Ketones. I. The Preparation of β-Ketodimethylacetals and Methoxymethylene Ketones | |
Mayo et al. | PHOTOCHEMICAL SYNTHESES: I. THE REACTION OF ALDEHYDES AND KETONES WITH CYCLOALKENES | |
Smith et al. | Kinetic Study of the Pyrolysis of 1, 2-Diarylethyl Acetates. IV1, 2 | |
Consiglio et al. | Nickel‐catalyzed Asymmetric Alkylation of Some Chiral and Achiral Allylic Alcohols. Preliminary communication | |
Meisters et al. | Exhaustive C-methylation of carboxylic acids by trimethylaluminium: A new route to t-butyl compounds | |
Klemm et al. | Alumina-catalyzed rreactions of hydroxyarenes and hydroaromatic ketones. I. Reactions of 1-naphthol with methanol | |
Erman | The condensation of camphene and phenol. Product formation via a direct 2, 6-hydride transfer | |
NISHIYAMA et al. | Anodic oxidation of some propenylphenols: synthesis of physiologically active neolignans | |
Adams et al. | 3-(Methylthio) propylborane, a distillable monoalkylborane | |
Baggaley et al. | Anodic oxidation. Part V. Some reactions with cyclohexa-1, 3-diene and cyclohexene | |
Howard et al. | Ketals of Monohydric Secondary Alcohols1 | |
GB1031221A (en) | Process for the production of trimethyl phosphite | |
Hampton et al. | Tetrasodio Bis-β-diketones. Dicondensations with Electrophilic Compounds1 | |
US2524778A (en) | butadiene-methylal addition | |
US2591239A (en) | 3-methoxy-4-methoxymethyl tetrahydropyran | |
Shabtai et al. | Alumina-catalyzed reactions of hydroxyarenes and hydroaromatic ketones. V. Mechanism of reduction of 1-tetralones to 1, 2-dihydronaphthalenes by means of methanol | |
Zakharkin et al. | Dimerization of isoprene in methanol using palladium complexes | |
US2883425A (en) | Method for preparing bicyclooctenones |