US3749618A - Process and solution for removing titanium and refractory metals and their alloys from tools - Google Patents
Process and solution for removing titanium and refractory metals and their alloys from tools Download PDFInfo
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- US3749618A US3749618A US00182209A US3749618DA US3749618A US 3749618 A US3749618 A US 3749618A US 00182209 A US00182209 A US 00182209A US 3749618D A US3749618D A US 3749618DA US 3749618 A US3749618 A US 3749618A
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- titanium
- tool
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- steel
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Classifications
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- 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
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F1/00—Etching metallic material by chemical means
- C23F1/10—Etching compositions
- C23F1/14—Aqueous compositions
- C23F1/16—Acidic compositions
- C23F1/26—Acidic compositions for etching refractory metals
-
- 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
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
- C23G1/04—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
- C23G1/06—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
Definitions
- titanium diflicult to machine
- the effect is cumulative with the deposit of a thin coat compounding the coating tendency and leading to complete seizing and galling of that portion of the tool which engages the workpiece.
- the tools are either discarded or the coated portion is mechanically cut ofi. and a suitable cutting edge is ground onto the end of the remaining portion.
- drill bits often as much as one inch must be removed to rid the bit of the titanium fused to it.
- the cost of tool bits for machining titanium is, accordingly, a significant factor in the cost of the machined product.
- One of the principal objects of the present invention is to provide a novel process and composition for removing titanium, refractory metals, and their alloys from tools without affecting the surface or other physical characteristics of the tool. Another object is to provide a process and composition for removing titanium fused to tool bits made of steel or carbides without destroying portions of the bits. A further object is to provide a process of the type stated Which consumes little time and does not require continued surveillance.
- the present invention comprises a solution for removing refractory metals and titanium and their alloys from tools made from ferrous metals and carbides and a process employing said solution.
- the solution is acidic and includes a source of fluoride ions, preferably hydrofluoric acid; water; a source of the COOH radical, preferably formic, oxalic, or tartaric acid, or mixtures thereof; and a corrosion inhibitor, preferably triethanolamine, ethylene glycol, or potassium iodide, or mixtures thereof.
- titanium covered tools are immersed in a hydrofluoric acid solution containing constituents which prevent the acid from attacking the tools metal and otherwise adversely affecting its sur- 3,749,618 Patented July 31, 1973 face, as well as other constituents for accelerating the dissolution of the titanium by the acid.
- hydrofluoric acid is a well known etchant for titanium and titanium alloys, it alone is not suitable for removing titanium from steel inasmuch as it also attacks the steel, leaving a pitted surface thereon.
- hydrofluoric acid alone requires considerable time to remove the last traces of titanium which are in intimate contact with the steel and, in addition, leaves a heavy black deposit, often called smut, on the steel.
- hydrofluoric acid is rendered suitable for removing titanium in intimate contact with steel by the addition of formic acid and triethanolamine to the hydrofluoric acid.
- the composition contains a source of fluoride ions, preferably hydrofluoric acid.
- a source of fluoride ions preferably hydrofluoric acid.
- suitable sources include fluoride salts, such as sodium or potassium fluoride.
- the weight percent of fluoride calculated as hydrofluoric acid is at least about 1%.
- the Weight percent of hydrofluoric acid may be increased up to about 10%, but extremely high concentrations may attack the tool, and the upper limit is dependent on the type of material from which the tool is made, the temperature of the reaction, and the nature of the other constituents of the solution, in addition to the concentration of the fluoride ions.
- hydrofluoric acid For removing titanium from tool steel, a concentration of hydrofluoric acid of 3.5% by weight (corresponding to 10% by volume of 70% hydrofluoric acid) is preferred and can be used safely without danger of pitting or otherwise disturbing the surface of the tool. This concentration is also satisfactory for other tool material.
- the tool materials to which this invention is applicable include: carbon steels, alloy steels, stainless steels, tool steels and tool materials known as carbides.
- carbides covers iron carbides, chromium carbides, tungsten carbides, and any other types of carbides.
- the source of the COOH radical preferably is formic acid, but oxalic acid and tartaric acid and a mixture thereof can be substituted in whole or in part for formic acid.
- Oxalic and tartaric acids are somewhat less effective than formic acid and other sources of COOH radical such as succinic, adipic, malonic, etc., can be used.
- Mono and dicarboxylic acids of 1-6 carbon atoms are suitable for use in this invention.
- the formic acid accelerates the dissolution of the titanium and, furthermore, effects removal of the last traces of titanium in intimate contact with the steel. To a limited extent, the formic acid also prevents the solution from attacking the steel. At least about 1% by weight formic acid is used in the composition. The preferred concentration is 2% formic acid by weight. The same weight percentages apply to oxalic and tartaric acids and other sources of COOH radical. Higher concentrations of formic acid can be used without any deleterious effects, but such higher concentrations produce no beneficial results and the excess is, therefore, merely superfluous. A practical upper limit of the COOH producing material is about 10% by weight (calculated as COOH radical).
- a metallic corrosion inhibitor in the amount of at least about 1% by weight and preferably about 2% by weight is included in the composition.
- This ingredient suitably may be triethanolamine, sodium nitrite, or potassium iodide or mixtures thereof, or other suitable corrosion inhibitors.
- the preferred ingredient is triethanolamine.
- the triethanolamine inhibits the hydrofluoric acid from attacking the steel and, in addition, prevents the formation of smut on the steel. Again, concentrations greater than 2% have no harmful effects nor does the excess produce any beneficial results. At least about 1% is necessary. Again, a practical upper limit is about 10% by weight.
- the temperature of the solution is not particularly critical with highly satisfactory results being obtained in the neighborhood of about 21 C.
- a practical temperature range is about 10 C. to about 33 C. Higher temperatures than indicated tend to produce some attack on steel and at lower temperatures the titanium removal rate becomes too slow to be practical.
- the titanium covered steel should remain in the solution until all of the titanium has dissolved.
- the duration of the immersion is dependent on the amount of titanium in contact with the steel. For conventional twist drills having moderate amounts of titanium seized and galled on their working surfaces, an immersion of from to 25 minutes in the solution is sufficient.
- dilute chromic solution less than about 1% chromic acid.
- Dilute chromic acid solution is used to prevent rusting of the chemically cleaned tool. If the steel forms part of a cutting tool, the cutting edges thereon can be resharpened at this point, and the tool is then in condition for use again with only a nominal amount of metal having been removed during the sharpening operation.
- the refractory metals include columbium, molybdenum, tungsten, and tantalum, and alloys thereof.
- this invention provides a process and composition for removing titanium and refractory metals and their alloys from a tool which achieves all of the objectives and advantages sought therefor.
- a composition for removing refractory metals and their alloys from a ferrous metal or carbide based tool without attacking the tool itself said composition being acidic and consisting essentially of from about 1% to about by weight of a source of fluoride ions calculated as hydrofluoric acid, from about 1% to about 10% 4 by weight of COOH radical provided by a COOH supplying material selected from the group consisting of mono and dicarboxylic acids of 1-6 carbon atoms, at least about 1% by weight of a metal corrosion inhibitor, and water.
- composition of claim 1 wherein the source of fluoride ions is hydrofluoric acid.
- composition of claim 1 wherein the corrosion inhibitor is selected from the group consisting of triethanolarnine, sodium nitrite, potassium iodide and mixtures thereof.
- composition of claim 1 including hydrofluoric acid as a source of fluoride ions, wherein the source of COOH radical is selected from the group consisting of formic acid, oxalic acid and tartaric acid, and mixtures thereof, and the corrosion inhibitor is selected from the group consisting'of triethanolamine, sodium nitrite, potassium iodide, and mixtures thereof.
- a process for removing titanium, refractory metals, and their alloys from ferrous metal or carbide based tools comprising the steps of: positioning a ferrous metal or carbide based tool having titanium, a refractory metal, or their alloys adhered to the working surface thereof into a solution containing from about 1% to about 10% by weight of a source of fluoride ions calculated as hydrofluoric acid, from about 1% to about 10% by weight of COOH radical provided by a COOH supplying material selected from the group consisting of mono and dicarboxylic acids of 1-6 carbon atoms, at least about 1% by weight of a metal corrosion inhibitor, and water; maintaining the tool in the solution until the adhered material has been removed by the composition; and removing the tool from the solution with the Working surface of the tool unaffected by the solution.
- hydrofluoric acid is the source of fluoride ions
- the source of COOH radical is selected from the group consisting of formic acid, oxalic acid, tartaric acid, and mixtures thereof
- the corrosion inhibitor is selected from the group consisting of triethanolamine, sodium nitrite, potassium iodide, and mixtures thereof.
- temperatures of the solution is from about 10 C. to about 33 C. during removal of material from the tool.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- ing And Chemical Polishing (AREA)
Abstract
TITANIUM AND REFRACTORY METALS AND THEIR ALLOYS ARE REMOVED FROM TOOLS, USUALLY MADE FROM STEEL OR CARBIDES, WITHOUT DELECTERIOUS EFFECTS ON THE TOOL BY IMMERSING THE COATED TOOL IN AN ACIDIC SOLUTION INCLUDING FLUORIDE IONS, WATER, A SOURCE OF COOH RADICAL, SUCH AS FORMIC, OXALIC, OR TARTARIC ACID, AND A CORROSION INHIBITOR, SUCH AS TRIETHANOLAMINE, POTASSIUM IODIDE, OR SODIUM NITRITE.
Description
United States Patent US. Cl. 156-3 8 Claims ABSTRACT OF THE DISCLOSURE Titanium and refractory metals and their alloys are removed from tools, usually made from steel or carbides, without deleterious effects on the tool by immersing the coated tool in an acidic solution including fluoride ions, Water, a source of COOH radical, such as formic, oxalic, or tartaric acid, and a corrosion inhibitor, such as triethanolamine, potassium iodide, or sodium nitrite.
REFERENCE TO OTHER APPLICATIONS This application is a continuation-in-part of our copending application Ser. No. 803,118, filed Feb. 27, 1969 now abandoned.
BACKGROUND OF THE INVENTION One of the primary reasons titanium is diflicult to machine is that it tends to fuse to and coat the tools used to machine it, thereby rendering their cutting edges ineffective. Furthermore, the effect is cumulative with the deposit of a thin coat compounding the coating tendency and leading to complete seizing and galling of that portion of the tool which engages the workpiece. Once coated, the tools are either discarded or the coated portion is mechanically cut ofi. and a suitable cutting edge is ground onto the end of the remaining portion. In the case of drill bits, often as much as one inch must be removed to rid the bit of the titanium fused to it. The cost of tool bits for machining titanium is, accordingly, a significant factor in the cost of the machined product.
One of the principal objects of the present invention is to provide a novel process and composition for removing titanium, refractory metals, and their alloys from tools without affecting the surface or other physical characteristics of the tool. Another object is to provide a process and composition for removing titanium fused to tool bits made of steel or carbides without destroying portions of the bits. A further object is to provide a process of the type stated Which consumes little time and does not require continued surveillance.
SUMMARY OF THE INVENTION The present invention comprises a solution for removing refractory metals and titanium and their alloys from tools made from ferrous metals and carbides and a process employing said solution. The solution is acidic and includes a source of fluoride ions, preferably hydrofluoric acid; water; a source of the COOH radical, preferably formic, oxalic, or tartaric acid, or mixtures thereof; and a corrosion inhibitor, preferably triethanolamine, ethylene glycol, or potassium iodide, or mixtures thereof.
DETAILED DESCRIPTION In practicing the present invention, titanium covered tools are immersed in a hydrofluoric acid solution containing constituents which prevent the acid from attacking the tools metal and otherwise adversely affecting its sur- 3,749,618 Patented July 31, 1973 face, as well as other constituents for accelerating the dissolution of the titanium by the acid. While hydrofluoric acid is a well known etchant for titanium and titanium alloys, it alone is not suitable for removing titanium from steel inasmuch as it also attacks the steel, leaving a pitted surface thereon. Moreover, hydrofluoric acid alone requires considerable time to remove the last traces of titanium which are in intimate contact with the steel and, in addition, leaves a heavy black deposit, often called smut, on the steel.
The foregoing disadvantages are eliminated and hydrofluoric acid is rendered suitable for removing titanium in intimate contact with steel by the addition of formic acid and triethanolamine to the hydrofluoric acid.
The composition contains a source of fluoride ions, preferably hydrofluoric acid. Other suitable sources include fluoride salts, such as sodium or potassium fluoride. The weight percent of fluoride calculated as hydrofluoric acid is at least about 1%. The Weight percent of hydrofluoric acid may be increased up to about 10%, but extremely high concentrations may attack the tool, and the upper limit is dependent on the type of material from which the tool is made, the temperature of the reaction, and the nature of the other constituents of the solution, in addition to the concentration of the fluoride ions.
For removing titanium from tool steel, a concentration of hydrofluoric acid of 3.5% by weight (corresponding to 10% by volume of 70% hydrofluoric acid) is preferred and can be used safely without danger of pitting or otherwise disturbing the surface of the tool. This concentration is also satisfactory for other tool material.
The tool materials to which this invention is applicable include: carbon steels, alloy steels, stainless steels, tool steels and tool materials known as carbides. The term carbides, as used here, covers iron carbides, chromium carbides, tungsten carbides, and any other types of carbides.
The source of the COOH radical preferably is formic acid, but oxalic acid and tartaric acid and a mixture thereof can be substituted in whole or in part for formic acid. Oxalic and tartaric acids are somewhat less effective than formic acid and other sources of COOH radical such as succinic, adipic, malonic, etc., can be used. Mono and dicarboxylic acids of 1-6 carbon atoms are suitable for use in this invention.
The formic acid accelerates the dissolution of the titanium and, furthermore, effects removal of the last traces of titanium in intimate contact with the steel. To a limited extent, the formic acid also prevents the solution from attacking the steel. At least about 1% by weight formic acid is used in the composition. The preferred concentration is 2% formic acid by weight. The same weight percentages apply to oxalic and tartaric acids and other sources of COOH radical. Higher concentrations of formic acid can be used without any deleterious effects, but such higher concentrations produce no beneficial results and the excess is, therefore, merely superfluous. A practical upper limit of the COOH producing material is about 10% by weight (calculated as COOH radical).
A metallic corrosion inhibitor in the amount of at least about 1% by weight and preferably about 2% by weight is included in the composition. This ingredient suitably may be triethanolamine, sodium nitrite, or potassium iodide or mixtures thereof, or other suitable corrosion inhibitors. The preferred ingredient is triethanolamine.
The triethanolamine inhibits the hydrofluoric acid from attacking the steel and, in addition, prevents the formation of smut on the steel. Again, concentrations greater than 2% have no harmful effects nor does the excess produce any beneficial results. At least about 1% is necessary. Again, a practical upper limit is about 10% by weight.
The temperature of the solution is not particularly critical with highly satisfactory results being obtained in the neighborhood of about 21 C. A practical temperature range is about 10 C. to about 33 C. Higher temperatures than indicated tend to produce some attack on steel and at lower temperatures the titanium removal rate becomes too slow to be practical.
Once immersed, the titanium covered steel should remain in the solution until all of the titanium has dissolved. Thus, the duration of the immersion is dependent on the amount of titanium in contact with the steel. For conventional twist drills having moderate amounts of titanium seized and galled on their working surfaces, an immersion of from to 25 minutes in the solution is sufficient.
After the steel is removed from the solution, it is rinsed clean in dilute chromic solution (less than about 1% chromic acid). Dilute chromic acid solution is used to prevent rusting of the chemically cleaned tool. If the steel forms part of a cutting tool, the cutting edges thereon can be resharpened at this point, and the tool is then in condition for use again with only a nominal amount of metal having been removed during the sharpening operation.
While the foregoing solution readily dissolves the titanium including even that titanium in intimate contact with the steel, it does not pit or otherwise adversely affect the surface of the steel, nor does it alter the steels mechanical properties.
SPECIFIC EXAMPLE Formic acid 2 Triethanolamine 2 Water 86 The refractory metals include columbium, molybdenum, tungsten, and tantalum, and alloys thereof.
Thus, it is seen that this invention provides a process and composition for removing titanium and refractory metals and their alloys from a tool which achieves all of the objectives and advantages sought therefor.
This invention is intended to cover all changes and modifications of the example of the invention herein chosen for purposes of the disclosure which do not constitute departures from the spirit and scope of the invention.
What is claimed is:
1. A composition for removing refractory metals and their alloys from a ferrous metal or carbide based tool without attacking the tool itself, said composition being acidic and consisting essentially of from about 1% to about by weight of a source of fluoride ions calculated as hydrofluoric acid, from about 1% to about 10% 4 by weight of COOH radical provided by a COOH supplying material selected from the group consisting of mono and dicarboxylic acids of 1-6 carbon atoms, at least about 1% by weight of a metal corrosion inhibitor, and water.
2. The composition of claim 1 wherein the source of fluoride ions is hydrofluoric acid.
3. The composition of claim 1 wherein the corrosion inhibitor is selected from the group consisting of triethanolarnine, sodium nitrite, potassium iodide and mixtures thereof.
4. The composition of claim 1 including hydrofluoric acid as a source of fluoride ions, wherein the source of COOH radical is selected from the group consisting of formic acid, oxalic acid and tartaric acid, and mixtures thereof, and the corrosion inhibitor is selected from the group consisting'of triethanolamine, sodium nitrite, potassium iodide, and mixtures thereof.
5. A process according to claim 4 and further characterized by rinsing the tool with dilute chromic acid solution after it is removed from the composition.
6. A process for removing titanium, refractory metals, and their alloys from ferrous metal or carbide based tools, comprising the steps of: positioning a ferrous metal or carbide based tool having titanium, a refractory metal, or their alloys adhered to the working surface thereof into a solution containing from about 1% to about 10% by weight of a source of fluoride ions calculated as hydrofluoric acid, from about 1% to about 10% by weight of COOH radical provided by a COOH supplying material selected from the group consisting of mono and dicarboxylic acids of 1-6 carbon atoms, at least about 1% by weight of a metal corrosion inhibitor, and water; maintaining the tool in the solution until the adhered material has been removed by the composition; and removing the tool from the solution with the Working surface of the tool unaffected by the solution.
7. The process of claim 6 wherein hydrofluoric acid is the source of fluoride ions, the source of COOH radical is selected from the group consisting of formic acid, oxalic acid, tartaric acid, and mixtures thereof, and the corrosion inhibitor is selected from the group consisting of triethanolamine, sodium nitrite, potassium iodide, and mixtures thereof.
8. The process of claim 6 wherein the temperatures of the solution is from about 10 C. to about 33 C. during removal of material from the tool.
References Cited UNITED STATES PATENTS 2,793,191 5/1957 Streicher 252-147 3,007,780 11/1961 Beigay et al 15620 3,108,919 10/1963 Bowman et a1. 156-18 3,413,205 11/1968 Hardman 204-441 JACOB H. STEINBERG, Primary Examiner 7 US. Cl. X.R.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US18220971A | 1971-09-20 | 1971-09-20 |
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US3749618A true US3749618A (en) | 1973-07-31 |
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US00182209A Expired - Lifetime US3749618A (en) | 1971-09-20 | 1971-09-20 | Process and solution for removing titanium and refractory metals and their alloys from tools |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3887403A (en) * | 1972-07-05 | 1975-06-03 | Mc Donnell Douglas Corp | Process and solution for removing titanium and refractory metals and their alloys from tools |
US3960741A (en) * | 1974-08-28 | 1976-06-01 | General Electric Company | Etchant for removing metals from glass substrates |
US4116755A (en) * | 1977-09-06 | 1978-09-26 | Mcdonnell Douglas Corporation | Chem-milling of titanium and refractory metals |
US4704126A (en) * | 1985-04-15 | 1987-11-03 | Richards Medical Company | Chemical polishing process for titanium and titanium alloy surgical implants |
US20060112972A1 (en) * | 2004-11-30 | 2006-06-01 | Ecolab Inc. | Methods and compositions for removing metal oxides |
WO2007140193A1 (en) * | 2006-05-25 | 2007-12-06 | Honeywell International Inc. | Selective tantalum carbide etchant, methods of production and uses thereof |
-
1971
- 1971-09-20 US US00182209A patent/US3749618A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3887403A (en) * | 1972-07-05 | 1975-06-03 | Mc Donnell Douglas Corp | Process and solution for removing titanium and refractory metals and their alloys from tools |
US3960741A (en) * | 1974-08-28 | 1976-06-01 | General Electric Company | Etchant for removing metals from glass substrates |
US4116755A (en) * | 1977-09-06 | 1978-09-26 | Mcdonnell Douglas Corporation | Chem-milling of titanium and refractory metals |
US4704126A (en) * | 1985-04-15 | 1987-11-03 | Richards Medical Company | Chemical polishing process for titanium and titanium alloy surgical implants |
US20060112972A1 (en) * | 2004-11-30 | 2006-06-01 | Ecolab Inc. | Methods and compositions for removing metal oxides |
US7611588B2 (en) | 2004-11-30 | 2009-11-03 | Ecolab Inc. | Methods and compositions for removing metal oxides |
WO2007140193A1 (en) * | 2006-05-25 | 2007-12-06 | Honeywell International Inc. | Selective tantalum carbide etchant, methods of production and uses thereof |
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