WO2006013643A1 - Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein - Google Patents
Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein Download PDFInfo
- Publication number
- WO2006013643A1 WO2006013643A1 PCT/JP2004/011659 JP2004011659W WO2006013643A1 WO 2006013643 A1 WO2006013643 A1 WO 2006013643A1 JP 2004011659 W JP2004011659 W JP 2004011659W WO 2006013643 A1 WO2006013643 A1 WO 2006013643A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- magnesium
- layer
- substituent
- acid
- forming
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21J—FORGING; HAMMERING; PRESSING METAL; RIVETING; FORGE FURNACES
- B21J1/00—Preparing metal stock or similar ancillary operations prior, during or post forging, e.g. heating or cooling
- B21J1/06—Heating or cooling methods or arrangements specially adapted for performing forging or pressing operations
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21J—FORGING; HAMMERING; PRESSING METAL; RIVETING; FORGE FURNACES
- B21J3/00—Lubricating during forging or pressing
Definitions
- the present invention relates to a method of warm plastic working of a magnesium alloy and a magnesium alloy (hereinafter abbreviated as “magnesium alloy”) and an intermediate used in the process.
- Gnesi ⁇ material is the lightest of all practical metals, its thin mouth
- ⁇ ⁇ has excellent specific strength, electromagnetic sealing, heat dissipation, vibration damping, etc., and has the advantage that less recycling energy is required for recycling.
- Magnesium bran is not cold-worked, but 20 ° C ⁇
- Warm plastic working is possible by heating to about 400 ° C and pressing. Usually, this is a place where the rolled material (stretched material) of magnetic brazing material is squeezed or bent. Then, mold with a press or a vender using a die.
- the processing temperature is 200 ° C or higher
- the lubricant may scorch the mold, the viscosity becomes high, and the processing such as squeezing is performed.
- progressive equipment since the processing temperature is 200 ° C or higher, the lubricant may scorch the mold, the viscosity becomes high, and the processing such as squeezing is performed. ⁇ Also, it is necessary to polish the mold in order to remove the lubricant and scorched carbide adhering every several to several tens of units, which is cumbersome and the production efficiency is poor.
- progressive equipment is 200 ° C or higher
- the purpose of the present invention is to eliminate such drawbacks of the prior art and to prevent the burning of the lubricant on the mold, and to reduce the number of times of the final cleaning of the mold.
- the first means of the present invention is to form a magnesium hydroxide layer on the surface of a magnetic layer made of magnesium or a magnetic alloy. In the process of forming a magnetic layer and an ink layer in the magnesium hydroxide layer, and forming the magnetic layer in a predetermined shape.
- the second means of the present invention is characterized in that, in the second means, the formation process of the magnesium hydroxide layer is a sub-phase.
- the magnesium hydroxide layer is formed by contacting an alkaline solution containing nitrate and the above-mentioned salt to form a magnesium hydroxide layer on the surface of the flake.
- the process of formation of an aliphatic strength ionic acid, including an aromatic strength or an aromatic strength rubonic acid It is characterized in that the S-hydroxylized hydroxide layer is brought into contact with the liquid and the magnesium hydroxide layer on the surface of the fork is reformed into a magnetic layer. Is a thing
- the aliphatic strength rubonic acid has no substituent or has a substituent, and the aliphatic group having 6 24 4 carbon atoms.
- the aromatic force rubonic acid is an organic compound selected from aromatic rubonic acid having no substituent or having a substituent and having a prime number of 7 20 It is characterized by and
- the organic compound is stearic acid.
- a fifth means of the present invention is characterized in that in the first means, an anodizing treatment step is provided after the inter-B plastic addition step.
- the sixth means of the present invention is a magnetic fork or a magnesium A
- the organic compound forming the magnesium-sodium soap layer has no substituent or has 6 to 6 carbon atoms having a substituent.
- Organization selected from 2 aliphatic rubonic acids of 4 or non-substituted or substituted aromatic rubonic acids having 7 20 carbon atoms 1 1 It is characterized by being a thing
- the eighth means of the present invention is characterized in that, in the seventh means, the oxide is a stearate salt.
- FIG. 1 is a diagram ⁇ ⁇ Cha ⁇ for clarifying the method of adding warm plasticity of magnesium bran according to the first embodiment of the present invention.
- Figure 2 is an enlarged cross-sectional view of a monolith with a magnesium hydroxide layer formed on the surface.
- Fig. 3 is an enlarged cross-sectional view of a steel plate with a magnesium soap layer formed on the surface.
- FIG. 4 is a schematic configuration diagram of a continuous press heating apparatus used in the embodiment of the present invention.
- Fig. 5 is a diagram ⁇ ⁇ ⁇ ⁇ for demonstrating the method of warm plastic addition of the magnetic slag according to the second embodiment of the present invention.
- Mg-A I 1 Zn system 1 1 3L
- Mg-A 1 system port SL has AM 100 A and so on physically.
- M g ⁇ As a rare earth element-based die, it is physically EZ 3 3 A, z E 4 1 A,
- the shape of the magnesium material is a plate, a tube, a rod, or a pellet.
- processing such as squeezing, bending, compression, tension, shearing, etc.
- it has no substituent, or has a substituent having a carbon number of 6 24, an aliphatic carboxylate, a non-substituent or a substituent. 7 to 2 carbon atoms
- a group of 0 aromatic strength rubonic acid salts can be used.
- the aliphatic chain may be a straight chain or a branched chain. It may be saturated or unsaturated.
- the number of carbons in the molecule is preferably ⁇ is 10 2 4, more preferably 8
- aliphatic strength rubonic acid of aliphatic strength rubonic acid salt examples include hexanoic acid 4-methylvaleric acid, 2-ethylbutyric acid, 2,2-dimethylbutyric acid, heptanoic acid Nanoic acid, repulsive acid, Riverside force acid,
- ⁇ -phosphate Li cystine acid, Pal Chin acid, hepta Ding force phosphate, steer-phosphate concentrated acid acid, base pair two phosphate, force 1 ⁇ Mel such as I Sosutea-phosphate.
- salts of aliphatic strength rubonic acid salts include, for example, alkali strength ⁇ s., Alkaline strength earth metal 1 ⁇ 2 & J salt, and ammonium salt.
- examples of the substituent of the aliphatic strength rubonic acid salt include a hydroxyl group, a strong ruxoxy group, an amino group, an alkoxy group, a acetyl group, and an octagonal atom.
- the number of substitutions is preferably 5 or less. ⁇ Is 3 or less, more preferably
- the number of carbons in the aromatic rubonic acid salt is preferably 7 to 20 and more preferably ⁇ 7 to 14.
- benzoic acid for example, benzoic acid, phthalic acid, isofartic acid, terephthalic acid, disulfuric acid, benzoic acid rubobo
- aromatic strength rubonic acid salts include gal strength metal 1 ⁇ 2 m, gal strength earth metal salt, amine salt, and ammonia salt.
- Metal strength, metal strength ⁇ SL ' ⁇ 1 ⁇ 2 ⁇ is preferred
- substituent of the aromatic power rubonate examples include a hydroxyl group, a strong ruboxy group, an amino group, a alkoxy group, a acetyl group, a non-gen atom, and an alkyl group having 16 carbon atoms. Number of substitutions is 5 or less, preferably
- exemplary preferred physical sensitizers for aromatic rubonic acid salts include sodium benzoate, sodium benzoate, lithium phthalate, sodium phthalate, and so on. There are, for example, sodium phthalate, sodium phthalate, etc.
- the lubricant of the present invention includes, for example, an anti-foaming agent, a viscosity adjusting agent, an antioxidant, an antifoaming agent, and an adjustment of the viscosity.
- Fig. 1 is a flow chart for explaining the method of plasticity between plates / magnesium according to the first embodiment.
- the concentration of the sodium nitrite solution is 50 g / l, 100 g / L, and the amount of sodium hydroxide added is 39 5 S.
- Fig. 2 is an enlarged cross-sectional view of ⁇ -k (alumi material) 2 in which a magnesium hydroxide layer 1 is formed on the entire surface. is there.
- the formation of the magnesium ⁇ soap layer is performed.
- the stearic acid sodium salt which is one of the above-mentioned aliphatic sulfonic acids, is added to the water.
- SC1 stearin that is heated to a temperature of 80 ° C to 100 ° C when the dissolved lubricant solution is added with water and hydroxylated water
- the concentration of the acid sodium solution is
- the magnesium hydroxide layer on the surface causes a chemical reaction in the lubricant solution when the H-treated pre-treated cake is immersed in the lubricant solution. ⁇ Form a number layer.
- the soaking time of the cake is 1 to 5 minutes.
- Fig. 3 shows a modification of the hydrogenated magnesium layer 1 and a magnetic layer V-ken layer on the entire surface.
- FIG. 3 is an enlarged cross-sectional view of a steel plate (aluminum material) 2 in which 3 is formed.
- This anodizing treatment consists of three steps of pretreatment, oxidation treatment and posttreatment.
- the pretreatment is a treatment to remove the lubricant adhering to the surface of the processed product. Since Magnesium ⁇ , which is an alkaline cleaning or acid cleaning, is resistant to alkalis, it can be effectively cleaned using a cleaning agent with a high degree of alkalinity. In the case of acid cleaning, it is better to use a cleaning agent with low acidity that does not damage the substrate. Consists of a mixed aqueous solution of length oil and sodium succinate, 75 ° C 8 0. Soak in a bathing bath maintained at c, and carry out 7 prescribed energizations in A. Aqueous solution of sodium oxalate and acid fluoride and sodium hydrate for a specified time.
- the post-treatment of the product is washed, dried and dried.
- ⁇ Oxide film functions as an anti-corrosion film for internal metal, and also serves as a base film for coating Therefore, after finishing the anodizing treatment, the coating finish of S6 is completed.
- FIG. 4 is a schematic configuration diagram of a continuous machining apparatus used in the present embodiment.
- a lower basin 5 is fixed on a base 4, and the lower basin 5 is gradually moved along the conveying direction X of the first step.
- a plurality of fixed-side molds 6 a 6 e with a recessed cross-section shape are attached.
- the movable side mold 10 0 a 1 has a cross-sectional shape with a gradually longer projecting dimension than the fixed side molds 26 & 6 e. 0 e is installed multiple times,
- nn degrees are controlled at 2100 ° C 3500 ° C / mi 1st.
- FIG. 6 is a diagram for explaining a work warm plastic working method according to the second embodiment of the present invention.
- the condition of formation of the magnesium hydroxide layer is as follows: R1 si washes the wet workpiece added with S 1, and formed a hydroxylated magnesium layer on the entire surface of S 1 with S 2 Same as the embodiment
- a lubricant solution in which stearic acid sodium hydroxide and hydroxide power lithium are dissolved is applied to the heated mold, and in S 4, the mold is pressed with the mold.
- the lubricant solution is separated from the magnesium hydroxide layer on the surface by the press pressure and the heat from the mold, and the magnetic layer is separated from the magnetic layer. Is formed.
- This magnesium-sodium soap layer functions as a lubricant in a process in which the press is pressed to form a flake into a predetermined shape.
- the process is anodized to form a dense oxide film on the surface (S 5), and then a paint finish is performed (S 6).
- a paint finish is performed (S 6).
- the hydroxide hydroxide layer or the magnesium alloy is used.
- the fork is submerged in the solution, but the solution can also be applied by applying the solution to the workpiece using a spine.
- the method of inter-plastic processing of a magnesium brazing material according to the present invention is, for example, a spine.
- -Power devices such as power cones and TV frames-Personal computers
- computers-Computer devices such as personal computers
- devices such as portable alpha-frames
- dental cameras Applicable to a variety of products such as optical equipment such as a lens, whirling steering force, and other white-wheeled vehicle parts.
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2004/011659 WO2006013643A1 (en) | 2004-08-06 | 2004-08-06 | Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein |
JP2006519264A JP4510819B2 (en) | 2004-08-06 | 2004-08-06 | Warm plastic working method of magnesium and magnesium alloy and intermediate used in the processing method |
CN2004800432724A CN1997472B (en) | 2004-08-06 | 2004-08-06 | Method of warm plastic forming of magnesium and magnesium alloy |
TW094123099A TWI281954B (en) | 2004-08-06 | 2005-07-08 | Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2004/011659 WO2006013643A1 (en) | 2004-08-06 | 2004-08-06 | Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006013643A1 true WO2006013643A1 (en) | 2006-02-09 |
Family
ID=35786944
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2004/011659 WO2006013643A1 (en) | 2004-08-06 | 2004-08-06 | Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP4510819B2 (en) |
CN (1) | CN1997472B (en) |
TW (1) | TWI281954B (en) |
WO (1) | WO2006013643A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015125737A1 (en) * | 2014-02-21 | 2015-08-27 | 日本パーカライジング株式会社 | Composition for direct-current cathodic electrolysis, lubrication-film-equipped metal material, and production method therefor |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5072861A (en) * | 1973-10-31 | 1975-06-16 | ||
JPS50104168A (en) * | 1974-01-25 | 1975-08-16 | ||
JPH03269092A (en) * | 1990-03-16 | 1991-11-29 | Daido Steel Co Ltd | Lubricant for cold and hot plastic processing |
JP2000144167A (en) * | 1998-11-05 | 2000-05-26 | Asahi Denka Kogyo Kk | Aqueous lubricating composition |
JP2001511423A (en) * | 1997-07-22 | 2001-08-14 | ゼネラル・モーターズ・コーポレーション | Lubrication system for thermoforming |
JP2002102986A (en) * | 2000-07-27 | 2002-04-09 | Hitachi Metals Ltd | Forming method for light metal material |
-
2004
- 2004-08-06 WO PCT/JP2004/011659 patent/WO2006013643A1/en active Application Filing
- 2004-08-06 JP JP2006519264A patent/JP4510819B2/en not_active Expired - Fee Related
- 2004-08-06 CN CN2004800432724A patent/CN1997472B/en not_active Expired - Fee Related
-
2005
- 2005-07-08 TW TW094123099A patent/TWI281954B/en not_active IP Right Cessation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5072861A (en) * | 1973-10-31 | 1975-06-16 | ||
JPS50104168A (en) * | 1974-01-25 | 1975-08-16 | ||
JPH03269092A (en) * | 1990-03-16 | 1991-11-29 | Daido Steel Co Ltd | Lubricant for cold and hot plastic processing |
JP2001511423A (en) * | 1997-07-22 | 2001-08-14 | ゼネラル・モーターズ・コーポレーション | Lubrication system for thermoforming |
JP2000144167A (en) * | 1998-11-05 | 2000-05-26 | Asahi Denka Kogyo Kk | Aqueous lubricating composition |
JP2002102986A (en) * | 2000-07-27 | 2002-04-09 | Hitachi Metals Ltd | Forming method for light metal material |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015125737A1 (en) * | 2014-02-21 | 2015-08-27 | 日本パーカライジング株式会社 | Composition for direct-current cathodic electrolysis, lubrication-film-equipped metal material, and production method therefor |
JPWO2015125737A1 (en) * | 2014-02-21 | 2017-03-30 | 日本パーカライジング株式会社 | Composition for direct current cathode electrolysis, metal material with lubricating film and method for producing the same |
Also Published As
Publication number | Publication date |
---|---|
TWI281954B (en) | 2007-06-01 |
CN1997472A (en) | 2007-07-11 |
CN1997472B (en) | 2010-05-26 |
JP4510819B2 (en) | 2010-07-28 |
TW200610839A (en) | 2006-04-01 |
JPWO2006013643A1 (en) | 2008-05-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101412245B1 (en) | Magnesium alloy member and method of manufacturing the same | |
JP4271573B2 (en) | Manufacturing method of metal wire for header processing | |
WO2015180500A1 (en) | Method for producing hot-plated product by hot rolling, direct cold rolling without pickling, and reduction annealing | |
CN101692382B (en) | Hydrogen removing method for radiator for transformer | |
JP2007284731A (en) | Method for manufacturing cold-forged article of aluminum alloy | |
WO2006013643A1 (en) | Method of warm plastic forming of magnesium and magnesium alloy, and intermediate for use therein | |
JP2006051801A (en) | Magnesium alloy plate for forming work, magnesium alloy case, and method for manufacturing magnesium alloy case | |
JP4932176B2 (en) | Machining method of magnesium or magnesium-based alloy | |
JP2013522466A (en) | Method for producing a coated metal strip | |
JP4734035B2 (en) | Intermediate of magnesium or magnesium-based alloy and method for producing the same | |
CN112126831A (en) | Bright anticorrosive aluminum profile and preparation method thereof | |
KR20220071291A (en) | Methods of preparing aluminum alloy products for bonding | |
WO2007023967A1 (en) | Method for production of magnesium alloy molding-processed article, and magnesium alloy molding-processed article | |
JP5237525B2 (en) | Treatment liquid for improving moldability of magnesium alloy plate, method for producing magnesium alloy plate using the same, and method for warm working | |
CN109689241A (en) | The molding roof rail of thermometal gas and its manufacturing method | |
KR100852452B1 (en) | Method of warm plastic forming of magnesium and magnesium alloy | |
CN107891248B (en) | Processing technology of battery pack magnesium alloy tray for new energy automobile | |
JP2007182633A (en) | Method of manufacturing anodized magnesium material, pretreatment composition for anodizing magnesium material and agent used for manufacturing the same | |
KR100688361B1 (en) | Apparatus for forming lubricant film in cold forging | |
JP3607832B2 (en) | Method for producing rolled copper foil with excellent wettability | |
JP2003055795A (en) | Method for producing thin product made of magnesium alloy | |
JPS5810973B2 (en) | Manufacturing method of plated steel wire | |
TW201037183A (en) | Method of manufacturing non-grinding type profile rail for use in linear motion guide unit | |
JP2006183089A (en) | Method for producing vibrator | |
CN108468049B (en) | Plastic deformation magnesium alloy surface sand surface treatment fluid and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200480043272.4 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006519264 Country of ref document: JP |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 1020067024890 Country of ref document: KR |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWP | Wipo information: published in national office |
Ref document number: 1020067024890 Country of ref document: KR |
|
122 | Ep: pct application non-entry in european phase |