CN102978503B - Inflammable sparking alloy and preparation method thereof - Google Patents

Inflammable sparking alloy and preparation method thereof Download PDF

Info

Publication number
CN102978503B
CN102978503B CN201210546855.5A CN201210546855A CN102978503B CN 102978503 B CN102978503 B CN 102978503B CN 201210546855 A CN201210546855 A CN 201210546855A CN 102978503 B CN102978503 B CN 102978503B
Authority
CN
China
Prior art keywords
inflammable
sparking alloy
alloy
sparking
magnesium
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 - Fee Related
Application number
CN201210546855.5A
Other languages
Chinese (zh)
Other versions
CN102978503A (en
Inventor
韦建松
徐国华
卢兰
卢颖
谢美萱
李宏伟
何沂桂
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Li Hongwei
Wei Jiansong
Xu Guohua
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201210546855.5A priority Critical patent/CN102978503B/en
Publication of CN102978503A publication Critical patent/CN102978503A/en
Application granted granted Critical
Publication of CN102978503B publication Critical patent/CN102978503B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention discloses an inflammable sparking alloy and a preparation method thereof. The inflammable sparking alloy contains 20 to 25 percent of lanthanum, 15 to 20 percent of cerium, 5 to 15 percent of tin, 35 to 45 percent of zinc, 1 to 5 percent of magnesium and 5 to 10 percent of iron. The preparation method sequentially comprises the following steps of: (1) weighing magnesium, cerium, tin, zinc, iron and magnesium serving as raw materials according to the mass percentage of each component in the inflammable sparking alloy, and cutting each component into small blocks; (2) putting the components into a smelting furnace together, and performing high-temperature smelting in a state of isolated oxygen; and (3) performing electromagnetic stirring and uniform mixing after the components are smelted, discharging, cooling ingots in the state of isolated oxygen, and thus obtaining the finished inflammable sparking alloy product. The inflammable sparking alloy product is stable in performance, low in ignition point and strong in abrasion resistance.

Description

A kind of inflammable sparking alloy and preparation method thereof
Technical field
The invention belongs to alloy preparation field, be specifically related to a kind of inflammable sparking alloy and preparation method thereof can be used in industry and daily life.
Background technology
The inflammable sparking alloy of rare earth is because its inflammable characteristic is widely used in industry and daily life, and in daily life, the inflammable sparking alloy of rare earth is mainly used in flint stone, is the important sources of lighter ignition.In defence and military, inflammable rare earth sparking alloy is processed into different elements, be respectively charged on different weapons, can obtain satisfied munitions effect.As in weapon for tracer bullet, bullet and shell draw core, portfire and other military applications etc.Other industrial aspect are processed into sparking alloy after element, can be used for industrial gas lamp, geordie, welding gun lighter for ignition and torch ignitor etc.
The inflammable sparking alloy of traditional rare earth is generally synthetic by rare earth or mishmetal, iron, magnesium, copper etc., because the content of alloy rare earth elements is often more than 70%, makes the cost of alloy very expensive; And rare earth element is very easily oxidized, the content in alloy is larger, because its oxidation is larger on the impact of quality product, reduces rare earth element and can not only reduce costs at the middle content of sparking alloy, also can improve the quality of products simultaneously; And rare earth resources is nonrenewable resources, deposit is in the world limited, even if China is the more country of content of rare earth, is also unable to undergo a large amount of Development patternss that use rare earth resources now; Therefore, seek the inflammable sparking alloy of a new generation that a kind of content of rare earth is lower and become development certainty.
Summary of the invention
The object of the invention is to for the deficiencies in the prior art, provide a kind of and reduced production costs ensureing, under the prerequisite of its performance, to reduce the usage quantity of rare earth, can be applicable to inflammable sparking alloy in industry and daily life and preparation method thereof.
To achieve these goals, the present invention has adopted following technical scheme:
A kind of inflammable sparking alloy, wherein: taking the quality of this inflammable sparking alloy as benchmark, described inflammable sparking alloy contains 20~25% lanthanum, 15~20% cerium, 5~15% tin, 35~45% zinc, 5~10% iron and 1~5% magnesium.
As each component concentration of inflammable sparking alloy of the present invention further preferably, taking the quality of this inflammable sparking alloy as benchmark, described inflammable sparking alloy contains 22~25% lanthanum, 15~18% cerium, 7~13% tin, 38~42% zinc, 5~8% iron and 1~5% magnesium.
As each component concentration of inflammable sparking alloy of the present invention further preferably, taking the quality of this inflammable sparking alloy as benchmark, described inflammable sparking alloy contains 23% lanthanum, 17% cerium, 10% tin, 40% zinc, 7% iron and 3% magnesium.
A method of preparing above-mentioned inflammable sparking alloy, comprises the following steps successively:
(1) according to each component of inflammable sparking alloy, the mass percent in inflammable sparking alloy takes raw material lanthanum, cerium, tin, zinc, iron and magnesium, then each component is cut into fritter;
(2) each component is dropped in smelting furnace together, then, under the state of isolation oxygen, carry out high melt; (furnace temperature in smelting furnace is up to more than 900 DEG C.)
(3) after the fusing of each component, adopt induction stirring to mix, to come out of the stove, the ingot casting of lowering the temperature under the state of isolation oxygen, can obtain the inflammable sparking alloy of finished product.
As the further illustrating of method of preparing inflammable sparking alloy in the present invention, the inflammable sparking alloy of above-described finished product is taking its quality as benchmark, contains 20~25% lanthanum, 15~20% cerium, 5~15% tin, 35~45% zinc, 5~10% iron and 1~5% magnesium.
As the further illustrating of method of preparing inflammable sparking alloy in the present invention, the inflammable sparking alloy of above-described finished product is taking its quality as benchmark, contains 23% lanthanum, 17% cerium, 10% tin, 40% zinc, 7% iron and 3% magnesium.
As the further illustrating of method of preparing inflammable sparking alloy in the present invention, above-described raw material lanthanum, cerium, tin, zinc, iron, magnesium all adopt simple substance as melting raw material.
As the further illustrating of method of preparing inflammable sparking alloy in the present invention, the state of above-described isolation oxygen is vacuum state, or the state in protection of inert gas.
Lanthanum (La), the content of lanthanum in the earth's crust is 0.00183%, is the abundantest one of content in rare earth element; , there is ductility argenteous soft metal; Heating energy burning, generates oxide compound and nitride; Can alloyage, also can make catalyzer.
Cerium (Ce), the metal that grey is active, is the highest one of natural abundance in lanthanide series metal, character is active; Can be used for manufacturing flint stone, pottery and alloy etc.
Tin (Sn), argenteous soft metal, proportion is 7.3, fusing point is low, only has 232 DEG C; Chemical property is very stable, is difficult for being at normal temperatures oxidized by oxygen, and is rich in malleability; Mainly for the manufacture of alloy, strengthen the wear resistance of alloy.
Zinc (Zn) is a kind of pearl opal metal.Density is 7.14 grams/cc, and fusing point is 419.5 DEG C.At room temperature, property is more crisp; 100~150 DEG C time, deliquescing; Exceed after 200 DEG C, become fragile again.The chemical property of zinc is active, and in air at normal temperatures, the zinc subcarbonate film that Surface Creation one deck is thin and fine and close, can stop further oxidation.When temperature reaches after 225 DEG C, zinc oxidation is fierce; Be mainly used in iron and steel, metallurgy, machinery, electric, chemical industry, light industry, military affairs and medicine and other fields.
Magnesium (Mg), argenteous metal, 1.738 grams/cc of density, 648.9 DEG C of fusing points, 1090 DEG C of boiling points; Be ductile, MAGNESIUM METAL is nonmagnetic, and has good heat dissipation; Can be for tobacco curing fire, flashlight powder, magnesium salts, vent fan, star shell etc.
The component lanthanum of inflammable sparking alloy, cerium are mainly to have played effect that alloy is got angry in the present invention, and rare-earth elements of lanthanum, cerium can generate with tin, zinc, iron, magnesium etc. the intermetallic compound of low ignition point; Add tin can fall the wear resistance of low-alloyed fusing point and increase alloy; Add a small amount of magnesium can strengthen the ignition quality of alloy; Part iron and zinc can also generate hard crisp FeZn compound, play the effect of putting forward heavy alloyed intensity, hardness; Zinc, as the matrix of alloy, has good ductility, can obviously put forward heavy alloyed erosion resistance, can also increase the density of alloy, has improved the extrusion processing performance of alloy.
Advantage of the present invention:
1. rare earth usage quantity is few, is only the half of traditional content, and production cost is low, and quality product is high.
2. product performance are stable, and according to detection, using the alloy density (ρ) that formula of the present invention and preparation method produce is 7.0g/cm 3~7.9g/cm 3, 170~180 DEG C of burning-points (T), hardness (HV) 140~160, sparking rate>=98%.
3. burning-point is low, wear resistance is strong; Due to the increase of tin, magnesium, zinc content, the fusing point of alloy, burning-point reduce, and ductility is good, and the corrosion resistance nature of alloy is obviously better than the inflammable sparking alloy of traditional rare earth.
Embodiment
Below in conjunction with embodiment, the present invention is further described, but do not limit the scope of the invention.
The content of each composition in inflammable sparking alloy (finished product), unit: %(weight percent):
? Lanthanum Cerium Tin Zinc Magnesium Iron
Embodiment 1 20 15 10 45 1 9
Embodiment 2 25 20 5 35 5 10
Embodiment 3 23 17 10 40 3 7
Embodiment 4 22 15 15 40 3 5
Embodiment 5 22 18 13 38 4 5
Embodiment 6 25 18 7 42 2 6
Embodiment 7 25 18 7 39 3 8
Embodiment 8 23 16 10 40 4 7
Embodiment 9 24 18 10 38 3 7
The preparation method of the inflammable sparking alloy of embodiment 1-5 comprises the following steps:
(1) according to each component of inflammable sparking alloy, the mass percent in inflammable sparking alloy takes the raw material simple substance of the components such as lanthanum, cerium, tin, zinc, iron and magnesium, then each component is cut into fritter;
(2) each component is dropped in smelting furnace together, then, under vacuum state, carry out high melt;
(3) after the fusing of each component, adopt induction stirring to mix, to come out of the stove, the ingot casting of lowering the temperature under vacuum state, can obtain the inflammable sparking alloy of finished product.
The preparation method of the inflammable sparking alloy of embodiment 6-9 comprises the following steps:
(1) according to each component of inflammable sparking alloy, the mass percent in inflammable sparking alloy takes the raw material simple substance of the components such as lanthanum, cerium, tin, zinc, iron and magnesium, then each component is cut into fritter;
(2) each component is dropped in smelting furnace together, then, under the state in protection of inert gas, carry out high melt;
(3) after the fusing of each component, adopt induction stirring to mix, to come out of the stove, the ingot casting of lowering the temperature under the state in protection of inert gas, can obtain the inflammable sparking alloy of finished product.
The inflammable sparking alloy finished product product performance of embodiment 1-9 are stablized, burning-point is low, wear resistance is strong.

Claims (8)

1. an inflammable sparking alloy, is characterized in that: taking the quality of this inflammable sparking alloy as benchmark, described inflammable sparking alloy contains 20~25% lanthanum, 15~20% cerium, 5~15% tin, 35~45% zinc, 1~5% magnesium and 5~10% iron.
2. inflammable sparking alloy according to claim 1, it is characterized in that: taking the quality of this inflammable sparking alloy as benchmark, described inflammable sparking alloy contains 22~25% lanthanum, 15~18% cerium, 7~13% tin, 38~42% zinc, 1~5% magnesium and 5~8% iron.
3. inflammable sparking alloy according to claim 1, is characterized in that: taking the quality of this inflammable sparking alloy as benchmark, described inflammable sparking alloy contains 23% lanthanum, 17% cerium, 10% tin, 40% zinc, 3% magnesium and 7% iron.
4. a method of preparing inflammable sparking alloy as claimed in claim 1, is characterized in that: the method comprises the following steps successively:
(1) according to each component of inflammable sparking alloy, the mass percent in inflammable sparking alloy takes raw material lanthanum, cerium, tin, zinc, iron and magnesium, then each component is cut into fritter;
(2) each component is dropped in smelting furnace together, then, under the state of isolation oxygen, carry out high melt;
(3) after the fusing of each component, adopt induction stirring to mix, to come out of the stove, the ingot casting of lowering the temperature under the state of isolation oxygen, can obtain the inflammable sparking alloy of finished product.
5. the method for the inflammable sparking alloy of preparation according to claim 4, it is characterized in that: the inflammable sparking alloy of described finished product is taking its quality as benchmark, contain 20~25% lanthanum, 15~20% cerium, 5~15% tin, 35~45% zinc, 1~5% magnesium and 5~10% iron.
6. the method for the inflammable sparking alloy of preparation according to claim 5, is characterized in that: the inflammable sparking alloy of described finished product is taking its quality as benchmark, contains 23% lanthanum, 17% cerium, 10% tin, 40% zinc, 3% magnesium and 7% iron.
7. the method for the inflammable sparking alloy of preparation according to claim 4, is characterized in that: described raw material lanthanum, cerium, tin, zinc, iron, magnesium all adopt simple substance as melting raw material.
8. the method for the inflammable sparking alloy of preparation according to claim 4, is characterized in that: the state of described isolation oxygen is vacuum state, or the state in protection of inert gas.
CN201210546855.5A 2012-12-17 2012-12-17 Inflammable sparking alloy and preparation method thereof Expired - Fee Related CN102978503B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210546855.5A CN102978503B (en) 2012-12-17 2012-12-17 Inflammable sparking alloy and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210546855.5A CN102978503B (en) 2012-12-17 2012-12-17 Inflammable sparking alloy and preparation method thereof

Publications (2)

Publication Number Publication Date
CN102978503A CN102978503A (en) 2013-03-20
CN102978503B true CN102978503B (en) 2014-08-13

Family

ID=47852837

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210546855.5A Expired - Fee Related CN102978503B (en) 2012-12-17 2012-12-17 Inflammable sparking alloy and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102978503B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104131244A (en) * 2014-07-08 2014-11-05 太原科技大学 Low burning point alloy ribbon and manufacturing method thereof
CN106834879A (en) * 2015-12-03 2017-06-13 黄波 A kind of pyrophoric alloy of element containing praseodymium and preparation method thereof
CN106834861A (en) * 2015-12-03 2017-06-13 黄波 A kind of lanthanum base firestone and preparation method thereof
CN106834862A (en) * 2015-12-03 2017-06-13 黄波 A kind of firestone of stable performance and preparation method thereof
CN106834859A (en) * 2015-12-03 2017-06-13 黄波 A kind of cerium base firestone and preparation method thereof
CN106834860A (en) * 2015-12-03 2017-06-13 黄波 A kind of pyrophoric alloy of neodymium element containing cerium and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB190908163A (en) * 1909-04-05 1910-03-17 Arthur George Bloxam Improved Manufacture of Pyrophoric Masses.
US3894867A (en) * 1974-01-09 1975-07-15 Us Navy Incendiary alloys existing as a dispersion of incendiary particles in a non-incendiary atmospheric attack-resistant matrix
CN102787257A (en) * 2012-08-20 2012-11-21 梁建烈 Novel mixed rare earth pyrophoric alloy and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB190908163A (en) * 1909-04-05 1910-03-17 Arthur George Bloxam Improved Manufacture of Pyrophoric Masses.
US3894867A (en) * 1974-01-09 1975-07-15 Us Navy Incendiary alloys existing as a dispersion of incendiary particles in a non-incendiary atmospheric attack-resistant matrix
CN102787257A (en) * 2012-08-20 2012-11-21 梁建烈 Novel mixed rare earth pyrophoric alloy and preparation method thereof

Also Published As

Publication number Publication date
CN102978503A (en) 2013-03-20

Similar Documents

Publication Publication Date Title
CN102978503B (en) Inflammable sparking alloy and preparation method thereof
CN102978504B (en) Inflammable alloy and preparation method thereof
CN102978502B (en) Rare-earth lanthanide series sparking alloy and preparation method thereof
CN102294485B (en) Composite electric contact material and preparation method thereof
CN104178673B (en) A kind of magnesium alloy and preparation method thereof
CN109332695B (en) Selective laser melting preparation method of molybdenum-based alloy with enhanced oxidation resistance
CN105385934A (en) Enamel pan and manufacturing process thereof
CN102321830A (en) Low-smelting point high-strength lead-bismuth rare earth alloy and preparation method thereof
AU2014202539A1 (en) Low-lead bismuth-free silicon-free brass
WO2015053820A1 (en) Ballistic zinc alloys, firearm projectiles, and firearm ammunition containing the same
CN102433489A (en) Aluminium-vanadium-tin-copper-iron intermediate alloy and preparation method thereof
EP2719785A1 (en) Ecological ammunition
CN105399328A (en) High-strength enamel pan and production technology thereof
WO2008091210A1 (en) A diffussion alloyed iron powder
CN102787257A (en) Novel mixed rare earth pyrophoric alloy and preparation method thereof
CN106541225B (en) Self-protection flux-cored wire and preparation method thereof suitable for oil-gas pipeline
CN103789569B (en) Bearing holder material and manufacture method thereof
WO2014062267A2 (en) Frangible projectile
CN103103425A (en) Heat resisting magnesium alloy
EP2913415A1 (en) Lead-free bismuth-free silicone-free brass
CN104789907A (en) Antifriction coating for metal surface and preparation method of antifriction coating
CN103911537A (en) Al-V-Cr-Fe-Ti intermediate alloy and preparation method thereof
CN106834860A (en) A kind of pyrophoric alloy of neodymium element containing cerium and preparation method thereof
CN106834861A (en) A kind of lanthanum base firestone and preparation method thereof
CN106834859A (en) A kind of cerium base firestone and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
ASS Succession or assignment of patent right

Owner name: WEI JIANSONG XU GUOHUA

Effective date: 20140627

C41 Transfer of patent application or patent right or utility model
C53 Correction of patent for invention or patent application
CB03 Change of inventor or designer information

Inventor after: Wei Jiansong

Inventor after: Xu Guohua

Inventor after: Lu Lan

Inventor after: Lu Ying

Inventor after: Xie Meixuan

Inventor after: Li Hongwei

Inventor after: He Yigui

Inventor before: Wei Jiansong

Inventor before: Xu Guohua

Inventor before: Lu Lan

Inventor before: Lu Ying

Inventor before: Xie Meixuan

Inventor before: Li Hongwei

COR Change of bibliographic data

Free format text: CORRECT: INVENTOR; FROM: WEI JIANSONG XU GUOHUA LU LAN LU YING XIE MEIXUAN LI HONGWEI TO: WEI JIANSONG XU GUOHUA LU LAN LU YING XIE MEIXUAN LI HONGWEI HE YIGUI

TA01 Transfer of patent application right

Effective date of registration: 20140627

Address after: 530006 Nanning East Road, the Guangxi Zhuang Autonomous Region, No. 188

Applicant after: Li Hongwei

Applicant after: Wei Jiansong

Applicant after: Xu Guohua

Address before: 530006 Nanning East Road, the Guangxi Zhuang Autonomous Region, No. 188

Applicant before: Li Hongwei

C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20140813

Termination date: 20141217

EXPY Termination of patent right or utility model