CN103265757A - Novel alloy - Google Patents
Novel alloy Download PDFInfo
- Publication number
- CN103265757A CN103265757A CN2013102125030A CN201310212503A CN103265757A CN 103265757 A CN103265757 A CN 103265757A CN 2013102125030 A CN2013102125030 A CN 2013102125030A CN 201310212503 A CN201310212503 A CN 201310212503A CN 103265757 A CN103265757 A CN 103265757A
- Authority
- CN
- China
- Prior art keywords
- alloy
- polypropylene
- magnesium
- following components
- wear resistant
- 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.)
- Granted
Links
Landscapes
- Lubricants (AREA)
Abstract
The invention relates to novel alloy. The novel alloy consists of main components and auxiliary components, wherein the main components consist of the following components in percentage by weight: 15%-25% of magnesium, 8%-16% of aluminum, 5%-10% of lithium, 1%-3% of cobalt, 5%-10% of nickel, 1%-5% of vanadium, 1%-2% of boron, 5%-8% of silicon and 0.5%-1% of titanium; the auxiliary components consist of the following components in percentage by weight: 25%-35% of polypropylene, 15%-25% of a lubricating agent, 10%-15% of inorganic minerals, wherein the melt flow rate of the polypropylene is 50g/minute. Compared with the prior art, the novel alloy has the advantages that (1), the magnesium alloy is not only lower in cost, but also simple in production process, easy to operate and control; (2), the magnetic alloy has better corrosion resistance, higher strength and certain flame resistance, and is relatively stable and capable of satisfying the requirements of electronic products, mechanical products and the like to a certain extent; and (3), the novel alloy has yield strength of 500MPa-600MPa, tensile strength of 1000MPa-1100MPa, HR30T70-HR30T78, and is suitable for rolling and forming of a building and electronic and mechanical machining and manufacturing with high hardness requirements, and good in bending performance.
Description
Technical field
The present invention relates to the alloy field, be specifically related to a kind of novel alloy and preparation method thereof.
Background technology
Magnesium is the lightest structured material, meets environmental protection, energy-conservation requirements such as less energy-consumption, thereby often is used to prepare alloy at industrial circles such as automobile, electronics, aviations.But the magnesium fusing point is low, easy firing, thereby the alloy that is prepared by magnesium self burning easily when temperature is near its burning-point, presence of fire danger.At present the material supply section that meets of preparation anti-flaming function commonly used is divided into compound, coating type and sandwich type three classes, above-mentioned three classes are respectively to add fire retardant in alloy, plate and on the alloy therebetween at alloy surface, but fire retardant mostly is toxic substance, and its use range of alloy that is prepared by this method is subjected to serious restriction.Although magnesium alloy is pursued well with the light ductility of its quality, owing to magnesium itself can react with water, air, so the magnesium alloy majority is not corrosion-resistant, and it can not use in harsh environment; Secondly, magnesium alloy can not satisfy the requirement of each side such as metallurgy, electronics, aviation in the prior art aspect wear-resisting, intensity and tension, therefore, limited the promotion and application of magnesium alloy to a certain extent.
Summary of the invention
The defective of the present invention in order to solve that magnesium alloy is inflammable and perishable, not wear-resisting, intensity is low etc. the invention provides a kind of novel alloy.Added boron and titanium in the technical program, the boron of trace forms BN in alloy, and poly-partially at austenite grain boundary, is conducive to reduce the alloy phase height.Ti is very strong solid N element, utilize the Ti fixing N below 0.006% in the steel just about 0.5%, form the TiN precipitated phase of tiny high-temperature stable, austenite crystal when this tiny TiN particle can hinder high temperature is effectively grown up, also help to improve the solid solubility of Nb in austenite, thus the strengthening effect that has improved alloy indirectly.
To achieve these goals, technical scheme of the present invention is achieved in that
A kind of novel alloy, it is characterized in that, described alloy is made up of main component and ancillary component, described main component is composed of the following components according to mass percent: magnesium 15-25%, aluminium 8-16%, lithium 5-10%, cobalt 1-3%, nickel 5-10%, vanadium 1-5%, boron 1-2, silicon 5-8%, titanium 0.5-1%, ancillary component is composed of the following components according to mass percent: polipropene 25-35%, lubricant 15-25%, inorganic mineral 10-15%, described polyacrylic melt flow rate (MFR) is 50g/min.
As a kind of improvement of the present invention, described lubricant is a kind of in silicon ester, the phosphoric acid ester.
As a kind of improvement of the present invention, described inorganic mineral is wollastonite.
As a kind of improvement of the present invention, described main component is composed of the following components according to mass percent: magnesium 18%, aluminium 13%, lithium 8%, cobalt 2%, nickel 8%, vanadium 3%, boron 1, silicon 6%, titanium 1%, ancillary component is composed of the following components according to mass percent: polypropylene 20%, lubricant 10%, inorganic mineral 10%, described polyacrylic melt flow rate (MFR) is 50g/min.
A kind of novel alloy, its preparation method comprises the steps:
(1) with described raw material, magnesium, aluminium, lithium, cobalt, nickel, vanadium, boron, silicon, titanium add even the stirring 10 minutes in the stirrer successively, carry out the melting of vacuum Medium frequency induction after stirring again, pour into a mould ingot casting, be milled into the Nanoalloy powder;
(2) with the Nanoalloy powder for preparing, with polypropylene, lubricant, inorganic mineral mixes, wherein earlier with 1/2nd polypropylene, a lubricant of/2nd, an inorganic mineral of/3rd mixes stirring 10 minutes, be heated to 150-180 °, again with remaining 1/2nd polypropylene, 1/2nd lubricant, 2/3rds inorganic mineral adds successively, use agitator to stir with 50 rev/mins speed, continue to be heated to 180-190 °, obtained Nanoalloy powder-polypropylene-inorganic mineral mixed solution in 30 minutes;
(3) with after the above-mentioned mixed solution homogenizing cast ingot, be that melting mixing is disperseed in the duplex bar forcing machine of 40:1 in length-to-diameter ratio, extrude difform alloy according to demand, described melt mix temperature is 190 ℃.
With respect to prior art, advantage of the present invention is as follows, 1) not only cost is lower for this magnesium alloy, and production technique simple, be easy to operate and control; 2) this magnesium alloy is corrosion-resistant better, intensity is higher, and has certain flame retardant resistance, more stable, satisfied the requirement of electronic product, engineering goods etc. to a certain extent, 3) this novel alloy yield strength is 500-600 MPa, tensile strength 1000-1100 MPa, HR30T 70-78, be applicable to electronics, mechanical workout making that building roll forming and high rigidity require, buckling performance is good.
Embodiment
Describe in further detail below in conjunction with the present invention of embodiment.Each components contents is weight percentage among the following embodiment except indicating especially
Embodiment 1
1.1 the preparation of novel alloy
(1) takes by weighing according to mass percent: magnesium 15%, aluminium 10%, lithium 5%, cobalt 3%, nickel 10%, vanadium 1%, boron 1%, silicon 5%, titanium 1%, add successively in the stirrer and evenly stirred 10 minutes, carry out the melting of vacuum Medium frequency induction after stirring again, pour into a mould ingot casting, be milled into the Nanoalloy powder;
(2) with the Nanoalloy powder for preparing, with polypropylene 24%, lubricant 16%, inorganic mineral 9% mixes, wherein earlier with 1/2nd polypropylene, a lubricant of/2nd, an inorganic mineral of/3rd mixes stirring 10 minutes, be heated to 150-180 °, again with remaining 1/2nd polypropylene, 1/2nd lubricant, 2/3rds inorganic mineral adds successively, use agitator to stir with 50 rev/mins speed, continue to be heated to 180-190 °, obtained Nanoalloy powder-polypropylene-inorganic mineral mixed solution in 30 minutes;
(3) with after the above-mentioned mixed solution homogenizing cast ingot, be that melting mixing is disperseed in the duplex bar forcing machine of 40:1 in length-to-diameter ratio, extrude difform alloy according to demand, described melt mix temperature is 190 ℃.
1.2 the erosion resistance of novel alloy
1.2.1 experimental group and control group are set:
The novel alloy that experimental group: embodiment 1 prepares
Control group 1:AS41B magnesium alloy
1.2.2 configuration solution and measuring method
Method according to ISO10271 is prepared pickling solution, namely adds (10.0 ± 0.1) g 90%C3H6O3(analytical pure in 300 mL distilled water) and (5.85 ± 0.005) g NaCl, then solution dilution to (1 000 ± 10) mL, pH is 2.3.
According to the standard of the corresponding 1 mL pickling solution of every square centimeter of alloy, add 6.5 mL pickling solutions in each Glass Containers; Tried in the vial that alloy is positioned over liquid feeding sealing with above-mentioned three groups; Take out censorship after in 37 ℃ constant water bath box, placing 7 d; (inductively coupled plasma atomicemission spectroscopy ICP-AES) measures magnesium ion concentration in each test tube to adopt inductive coupling plasma emission spectrograph.
Organized by examination | Experimental group | Control group 1 |
Magnesium density g/l | 0 | (158.1±48.6)×10 -6 |
1.3 the flame retardant effect of novel alloy.
Method with embodiment 1 prepares the novel alloy of sheet as experimental group, the AS41B magnesium alloy is organized 2 in contrast, above-mentioned two kinds of alloys are melted respectively at crucible, utilize EVOC PCI DAS temperature acquisition card collecting temperature, utilize computer to determine combustion initiation temperature.
Organized by examination | Experimental group | Control group 2 |
Combustion initiation temperature | 930℃ | 420℃ |
1.4 the hardness of novel alloy
As experimental group, the AS41B magnesium alloy is organized 2 in contrast with the wear resistant alloy of the method for embodiment 1 preparation, surveys two groups of hardness of alloy respectively and stretch slightly, contrast as follows:
Organized by examination | Experimental group | Control group 2 |
Hardness | 30HRC | 18HRC |
Tensile strength | 1000—1100MPa | 600 MPa |
Yield strength | 500—600 MPa | 400 MPa |
1.5 result
As can be seen, the novel alloy of embodiment 1 preparation have good anti-corrosion and flame retardant effect, and its wear resistance is better, and hardness is higher, and range of application is more extensive.
Embodiment 2
Preparation method is identical with disclosed mode among the embodiment 1, but the main component of the alloy in the present embodiment is composed of the following components according to mass percent: magnesium 22%, aluminium 8%, lithium 5%, cobalt 1%, nickel 6%, vanadium 1%, boron 1%, silicon 5.5%, titanium 0.5%, ancillary component is composed of the following components according to mass percent: polipropene 25 %, phosphoric acid ester 15%, wollastonite 10%.
Embodiment 3
Preparation method is identical with disclosed mode among the embodiment 1, but the main component of the alloy in the present embodiment is composed of the following components according to mass percent: magnesium 18%, aluminium 13%, lithium 8%, cobalt 2%, nickel 8%, vanadium 3%, boron 1, silicon 6%, titanium 1%, ancillary component is composed of the following components according to mass percent: polypropylene 20%, phosphoric acid ester 10%, wollastonite 10%.
The above; only be to preferred embodiment of the present invention; be not that the present invention is done other forms of restriction; any those skilled in the art may utilize the technology contents of above-mentioned announcement to be changed or be modified as the equivalent embodiment of equal variation; every disengaging the present invention program content; according to any simple modification that technical spirit of the present invention is done above embodiment, equivalent variations and remodeling all drop in protection scope of the present invention.
Claims (6)
1. wear resistant alloy, it is characterized in that, described alloy is made up of main component and ancillary component, described main component is composed of the following components according to mass percent: magnesium 15-25%, titanium 8-13%, lithium 10-15%, cobalt 1-5%, nickel 10-25%, manganese 3-5%, yttrium 0.5-2%, tungsten 5-10%, vanadium 1-5%; Ancillary component is composed of the following components according to mass percent: polypropylene 10%-20%, and lubricant 1-10%, inorganic mineral 1-10%, described polyacrylic melt flow rate (MFR) is 70g/min.
2. wear resistant alloy according to claim 1 is characterized in that, described lubricant is a kind of in silicon ester, the phosphoric acid ester.
3. wear resistant alloy according to claim 1 is characterized in that, described mineral substance is wollastonite.
4. according to the described wear resistant alloy of claim 1-3, it is characterized in that described main component is composed of the following components according to mass percent: magnesium 20%, titanium 10%, lithium 12%, cobalt 3%, nickel 15%, manganese 4%, yttrium 1%, tungsten 8%, vanadium 3%; Ancillary component is composed of the following components according to mass percent: polypropylene 15%, lubricant 5%, inorganic mineral are 4%.
5. according to the described wear resistant alloy of claim 1-3, its preparation method comprises the steps:
(1) according to the quality proportioning of mentioned component, earlier with magnesium, titanium, lithium, cobalt, nickel, manganese, yttrium, tungsten, vanadium mix the back and stir, after stirring in a vacuum frequently induction melting, pour into a mould ingot casting, be milled into the Nanoalloy powder;
(2) with the Nanoalloy powder for preparing, with 1/2nd polypropylene, 1/3rd lubricants, 1/2nd inorganic mineral, mix, use agitator to stir with 30-50 rev/mins speed,
(3) stir after 20 minutes, add 1/2nd polypropylene successively, 2/3rds lubricants, 1/2nd inorganic mineral, Heating temperature to 150-200 a ° stirring obtained Nanoalloy powder-polypropylene-inorganic mineral mixed solution in 15-25 minutes;
(4) with after the above-mentioned mixed solution homogenizing cast ingot, be that melting mixing is disperseed in the duplex bar forcing machine of 50:1 in length-to-diameter ratio, extrude difform alloy according to demand, described melt mix temperature is 180 ℃.
6. according to the purposes of the described wear resistant alloy of claim 1-3, it is characterized in that, for the preparation of wear-resisting container.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310212503.0A CN103265757B (en) | 2013-05-31 | 2013-05-31 | Novel alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310212503.0A CN103265757B (en) | 2013-05-31 | 2013-05-31 | Novel alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
CN103265757A true CN103265757A (en) | 2013-08-28 |
CN103265757B CN103265757B (en) | 2015-04-29 |
Family
ID=49009427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201310212503.0A Expired - Fee Related CN103265757B (en) | 2013-05-31 | 2013-05-31 | Novel alloy |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103265757B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107178316A (en) * | 2017-07-14 | 2017-09-19 | 郭甜甜 | A kind of high agriculture grinding drill of hardness |
CN107366508A (en) * | 2017-07-14 | 2017-11-21 | 郭甜甜 | A kind of wear-resisting grinding drill |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101235173A (en) * | 2008-02-22 | 2008-08-06 | 南京信息工程大学 | Magnesium particle macromolecule composite material and preparation method thereof |
-
2013
- 2013-05-31 CN CN201310212503.0A patent/CN103265757B/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101235173A (en) * | 2008-02-22 | 2008-08-06 | 南京信息工程大学 | Magnesium particle macromolecule composite material and preparation method thereof |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107178316A (en) * | 2017-07-14 | 2017-09-19 | 郭甜甜 | A kind of high agriculture grinding drill of hardness |
CN107366508A (en) * | 2017-07-14 | 2017-11-21 | 郭甜甜 | A kind of wear-resisting grinding drill |
Also Published As
Publication number | Publication date |
---|---|
CN103265757B (en) | 2015-04-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103266254A (en) | Wear-resistant alloy | |
CN102127658B (en) | Method for preparing high-purity aluminum-vanadium intermediate alloy | |
CN104043821B (en) | Resistant corrosion-resistant spray-coating powder and preparation method thereof | |
CN103266255B (en) | High-temperature-resistant oxidation-resistant alloy | |
CN102634718A (en) | Preparation process for organically-combined fluorite ball | |
CN103265757B (en) | Novel alloy | |
CN101135021A (en) | Aluminium magnesium ferroalloy for molten steel deoxidization desulfuration and alloying and preparation method thereof | |
CN101831104B (en) | Plastic welding rod | |
CN103266253B (en) | High-temperature-resistant alloy | |
CN102418094A (en) | Low-temperature phosphating concentrate and low-temperature phosphating technology for cold forming processing | |
CN103571996B (en) | Smelt Vanadium Microalloyed Plate Steels and increase vanadium barium oxide cored-wire and preparation method thereof | |
CN103266256A (en) | High-toughness and anticorrosive plastic alloy | |
CN103233151A (en) | High creep resistance quasicrystal-containing double phase magnesium-lithium alloy and preparation method thereof | |
CN103266250B (en) | Flame retardant corrosion-resisting alloy | |
CN101974703A (en) | Copper alloy and copper alloy product | |
CN104726640A (en) | Composite vanadium-nitrogen additive for deformed steel bar production | |
CN101787414B (en) | Composite deoxidizer for steelmaking and preparation method thereof | |
CN105734337A (en) | Wearing-resistant cooper alloy mold material | |
CN102839309A (en) | Mixing method for preparing high-strength high-tenacity molybdenum alloy | |
CN111496245B (en) | High-corrosion-resistance powder material and preparation method and application thereof | |
CN109401366A (en) | A kind of Cu-Zn alloy powder resistant to high temperature | |
CN101333061B (en) | Conveying process for liquid crystal glass primary materials | |
CN101265528B (en) | Dispersing agent for aluminum titanium boron production and preparation method thereof | |
CN105970024A (en) | Abrasion-resistant composite material for automobile brake pads | |
CN103265751B (en) | Corrosion-resistant alloy |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20150429 |