CN101613082A - A kind of manufacture method of producing the aluminium alloy of hydrogen - Google Patents
A kind of manufacture method of producing the aluminium alloy of hydrogen Download PDFInfo
- Publication number
- CN101613082A CN101613082A CN200810115694A CN200810115694A CN101613082A CN 101613082 A CN101613082 A CN 101613082A CN 200810115694 A CN200810115694 A CN 200810115694A CN 200810115694 A CN200810115694 A CN 200810115694A CN 101613082 A CN101613082 A CN 101613082A
- Authority
- CN
- China
- Prior art keywords
- aluminium
- gallium
- powder
- alloy
- aluminum
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
Landscapes
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
Abstract
The present invention relates to a kind of manufacture method of aluminium alloy, make a kind of aluminium alloy that can produce hydrogen with the technology of powder metallurgy, this aluminium alloy is stable in the air, meets water generates hydrogen.The aluminium alloy main component is a metallic aluminium, and submember is a gallium, and metallic aluminium can total overall reaction produce hydrogen.
Description
Technical field
The present invention relates to a kind of gallium aluminium metal of using and make aluminium alloy a kind of and water reaction generation hydrogen by powder metallurgy technology.This aluminium alloy and water reaction can produce hydrogen efficiently, rapidly, completely, can be used in the automobile of combustion hydrogen engine or all kinds of automobiles of hydrogen fuel cell, also can give emergent portable power generation machine hydrogen supply to drive wheelchair, golf cart, small agricultural machinery, battlefield robot etc., also can provide hydrogen source to keep the health of environment for the combustion hydrogen engine at enclosed space (as submarine), in a word, as long as water filling just can produce the extraordinary aluminium alloy of hydrogen and have broad application prospects, be the essential product of social life in the future.
Technical background
Along with exhausting day by day of oil and coal resource and growing to even greater heights of price, the requirement that urban environment is administered, the alternative energy of environmental protection is extremely urgent demand.In the face of the recoverable amount of nearly 1,000,000,000 cars in the whole world, automobile accounts for more than 50% the consumption of fuel oil, also is the primary pollution source of urban air, and acting as a fuel with hydrogen is a selection, thereby the solution on-board hydrogen source has more urgency.The advantage of aluminium alloy hydrogen manufacturing mainly is to improve the level of safety with hydrogen with avoiding the obstacle of hydrogen storage and transportation.Can certainly provide hydrogen source to hydrogen fuel cell, to obtain needed electric energy.The essence that aluminium alloy produces hydrogen is that the form of electric energy with metallic aluminium stored, and the effect of rechargeable battery is played in the use of portable convenient.Along with the raising of oil and coal price lattice with exhaust and environmental protection requirement, the advantage of nuclear power shows gradually, and utilizing nuclear power can be the thing of an economic environmental protection with producing the alumina eltrolysis regeneration that obtains behind the hydrogen.
The China's Aluminum ore reserves is very abundant, compares with various non-ferrous metals, and the content of aluminium in aluminum ore is much higher, has bigger advantage on resource.And the aluminium hydroxide that generates easily is converted into aluminum oxide, produces aluminium than from alum clay mineral products aluminium considerably cheaper by aluminum oxide, compares with gasoline to have very strong price competitiveness, and as the gallium of dissipated metal, China is rich in minerals, has possessed resources supplIes well.In bauxite and zink sulphide, generally all be rich in gallium element, and with common chemical process, just reach 3N purity (99.9%) easily, satisfy the requirement of gallium purity in the alloy, more much lower than used gallium purity in photoelectron and the semiconductor material, also considerably cheaper; Fusing point is 29.78 ℃, and boiling point is 2070 ℃, and gallium is an inert metal, and is stable in the air under the normal temperature, does not react with water, and this provides convenience for the practical application of gallium.
The present domestic similar techniques of still not having.
Summary of the invention
The present invention relates to a kind of preparation of particular aluminum alloy, the metal that plays active function may also extend into other metal except gallium metal, and as zinc, indium, germanium, boron etc., their preparation method is similar.With superfine metal aluminium powder and gallium metal is raw material, and the foam metallurgical method by easy economy by technology such as high pressure, sintering, moulding, has obtained a kind of alloy that can produce hydrogen rapidly, efficiently, completely.Generally in inert atmosphere or nitrogen atmosphere, carry out rare gas element such as argon gas, nitrogen, helium etc. when preparing this class alloy.
Metallic aluminium forms fine and close sull in air, can form aluminum hydroxide precipitation and continue and the water reaction to stop aluminium attached to the aluminum metal surface in water, and principle of the present invention avoids both of these case to occur exactly.Thereby the surface coverage gallium at metallic aluminium makes it and the isolated reactive behavior that keeps metallic aluminium of air; Eliminate aluminum hydroxide precipitation and realize by two measures, the one, aluminium hydroxide is dissolved in the solution of gallium hydroxide, and the 2nd, in water, add sequestrant dissolved hydrogen aluminum oxide, make metallic aluminium continue to generate hydrogen thereby make it not form aluminum hydroxide precipitation with the water reaction.
The acquisition of metal-powder is generally undertaken by efficient ball mill under inert atmosphere or nitrogen atmosphere, the granularity of metal-powder generally at 50 orders between 3000 orders, definite by sieving; The metal-powder of determining granularity is mixed with gallium by certain weight ratio, casting knot under certain pressure is perhaps tied metal-powder casting earlier or sintering, is dipped in the liquid metal gallium again, make gallium can cover the metallic aluminium surface fully, thereby obtain the powder metallurgy solid piece with secluding air.These powder metallurgy solids can be determined microtexture by X-ray diffraction.
The powder metallurgy solid that obtains is placed the device of similar kipp gas generator, add the entry or the aqueous solution, reaction produces hydrogen.The process of reaction can freely be controlled with the pressure of hydrogen, and is complete up to the metallic aluminium total overall reaction.Containing in the aqueous solution can aluminium chelate ionic sequestrant, as deferoxamine mesylate, and oxysuccinic acid etc.Gallium and water reaction at a certain temperature produces gallium hydroxide, and gallium hydroxide solution is alkalescence, can the dissolved hydrogen aluminum oxide, make it to be not attached to the metallic aluminium surface, thus make metallic aluminium can with the water sustained reaction.
After metal aluminium plus gallium and water react completely, with resultant heating, obtain metal oxide, chemical purification can the secondary metal gallium, and aluminum oxide can electrolytic regeneration aluminium.In a word, essence of the present invention is a kind of energy storage equipment, and is easy to use as the energy of mobile equipment, economic environmental protection.
Example 1 obtains the aluminium powder 50g of 200--400 order granularity by ball mill in inert atmosphere, stirs to join in the 15g Gallium solution, and congruent melting (molten), cooling reaches the blend of crystallite phase gradually, obtains alloy body 65g.In kipp gas generator, alloy body and 30 ℃ of water react, and produce hydrogen.The reacting weight that metering gas is converted to aluminium is 98.7.
Example 2 joins the stirring of 10g Gallium solution among the aluminium powder 50g of 50-100 order granularity in inert atmosphere, and Gallium solution is covered aluminium powder fully, and cooling forms alloy body 60g.In kipp gas generator, alloy body and 30 ℃ of water react, and produce hydrogen.The reacting weight that metering gas is converted to aluminium is 96.7.
Example 3 with the aluminium powder 50g oxyhydrogen flame sinter molding of 100--200 order granularity, covers the aluminium powder piece surface of moulding with the 10g Gallium solution in inert atmosphere, accomplish to cover fully, and cooling obtains solid alloy.In kipp gas generator, the alloy body and the aqueous solution react, and produce hydrogen, contain the chelate aluminum ion mixture in the aqueous solution, and concentration is 20% (molar percentage), and sequestrant is deferoxamine mesylate or oxysuccinic acid.The reacting weight that metering gas is converted to aluminium is 97.8.
Claims (6)
- The preparation method of 1 one kinds of aluminum gallium alloys, this aluminum gallium alloy can react with water, and the aluminium total overall reaction produces hydrogen.
- The preparation method of 2 one kinds of described compounds of claim 1 is characterized in that powder metallurgy, and this method comprises following each step:1) in inert atmosphere, be generally argon gas or nitrogen,, sieve metallic aluminium mechanical disintegration powdered with ball mill or other instruments, determine powder size, between the 500-10 order;2) in inert atmosphere, be generally argon gas or nitrogen; Temperature is below the fusing point of aluminium, with 1) powder hot-cast moulding, obtain the floury texture metallic aluminium, and this metal aluminum blocks be soaked in the liquid metal gallium, temperature is between 2000--30 ℃, the cooling, obtain aluminum gallium alloy;3) in inert atmosphere, be generally argon gas or nitrogen; With 1) powder join in the hot liquid gallium, temperature is between 2000--30 ℃, stir, die casting, cooling obtains gallium aluminium and closes powder metallurgy;4) in inert atmosphere, be generally argon gas or nitrogen; With 1) powder and the powder of gallium heat altogether, temperature is between 2000--30 ℃, obtains aluminum gallium alloy after the cooling.
- 3 in right 2 in the preparation of aluminum gallium alloy, and aluminium: the weight ratio scope of gallium was at 95: 5 to 50: 50, and the purity of gallium aluminium metal can be electronic-grade purity, also can be general industry product purity.
- 4 in right 2 in the preparation of aluminum gallium alloy, and inert atmosphere refers to a kind of or two kinds and the above mixture in nitrogen, helium, the argon gas.
- 5 in the process that produces hydrogen, and the water that reacts with aluminium alloy comprises common daily water consumption, also comprises the aqueous solution that contains extraordinary sequestrant.
- 6 sequestrants of mentioning in right 5 comprise chelate aluminum ion mixture such as deferoxamine mesylate or oxysuccinic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200810115694A CN101613082A (en) | 2008-06-27 | 2008-06-27 | A kind of manufacture method of producing the aluminium alloy of hydrogen |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200810115694A CN101613082A (en) | 2008-06-27 | 2008-06-27 | A kind of manufacture method of producing the aluminium alloy of hydrogen |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101613082A true CN101613082A (en) | 2009-12-30 |
Family
ID=41492994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200810115694A Pending CN101613082A (en) | 2008-06-27 | 2008-06-27 | A kind of manufacture method of producing the aluminium alloy of hydrogen |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101613082A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103233145A (en) * | 2013-03-21 | 2013-08-07 | 燕山大学 | Aluminum-gallium alloy and preparation method thereof |
CN105112945A (en) * | 2015-09-18 | 2015-12-02 | 安徽工业大学 | Method for preparing hydrogen production aluminum-gallium alloy by utilizing molten salt electrolysis codeposition |
CN105600748A (en) * | 2015-12-29 | 2016-05-25 | 杜善骥 | Working method of submersible type aluminum-gallium alloy hydrogen manufacturing unit |
CN106698338A (en) * | 2015-11-12 | 2017-05-24 | 中国科学院理化技术研究所 | Liquid metal assisted aluminum block direct hydrogen production device and application thereof |
CN106788376A (en) * | 2015-11-19 | 2017-05-31 | 中国科学院理化技术研究所 | Self-excited oscillation device, Fluid valve, contactor and light path switch |
WO2022160390A1 (en) * | 2021-01-27 | 2022-08-04 | 苏州大学 | Method for preparing deuterium gas and deuteration reaction using same as deuterium source |
-
2008
- 2008-06-27 CN CN200810115694A patent/CN101613082A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103233145A (en) * | 2013-03-21 | 2013-08-07 | 燕山大学 | Aluminum-gallium alloy and preparation method thereof |
CN103233145B (en) * | 2013-03-21 | 2015-07-22 | 燕山大学 | Aluminum-gallium alloy and preparation method thereof |
CN105112945A (en) * | 2015-09-18 | 2015-12-02 | 安徽工业大学 | Method for preparing hydrogen production aluminum-gallium alloy by utilizing molten salt electrolysis codeposition |
CN106698338A (en) * | 2015-11-12 | 2017-05-24 | 中国科学院理化技术研究所 | Liquid metal assisted aluminum block direct hydrogen production device and application thereof |
CN106698338B (en) * | 2015-11-12 | 2018-11-02 | 中国科学院理化技术研究所 | A kind of liquid metal auxiliary aluminium block direct hydrogen production device and its application |
CN106788376A (en) * | 2015-11-19 | 2017-05-31 | 中国科学院理化技术研究所 | Self-excited oscillation device, Fluid valve, contactor and light path switch |
CN106788376B (en) * | 2015-11-19 | 2019-09-17 | 中国科学院理化技术研究所 | Self-excited oscillation device, Fluid valve, circuit switch and light path switch |
CN105600748A (en) * | 2015-12-29 | 2016-05-25 | 杜善骥 | Working method of submersible type aluminum-gallium alloy hydrogen manufacturing unit |
WO2022160390A1 (en) * | 2021-01-27 | 2022-08-04 | 苏州大学 | Method for preparing deuterium gas and deuteration reaction using same as deuterium source |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Liu et al. | Issues and opportunities facing hydrolytic hydrogen production materials | |
Tan et al. | Hydrogen generation via hydrolysis of Mg2Si | |
CN101597048B (en) | Method for preparing anode material lithium iron phosphate | |
CN101613082A (en) | A kind of manufacture method of producing the aluminium alloy of hydrogen | |
CN102409202A (en) | Al-Ga-In-Sn-Zn alloy as well as preparation method and application thereof | |
US20120275981A1 (en) | Preparation Of Silicon For Fast Generation Of Hydrogen Through Reaction With Water | |
Chen et al. | Hydrogen generation from splitting water with Al–Bi (OH) 3 composite promoted by NaCl | |
CN108193107B (en) | Preparation method of organic coated core-shell nano composite hydrogen storage material | |
CN102277508A (en) | Preparation method of magnesium-based hydrogen storage alloy | |
CN102390805A (en) | Hydrogen production composition and preparation method thereof, and method for preparing hydrogen | |
CN101891151A (en) | Magnesium-aluminum based hydride composite material for hydrolytic hydrogen production | |
US8808663B2 (en) | Hydrogen generation using compositions including magnesium and silicon | |
Li et al. | Hydrogen generation performance of novel Al–LiH–metal oxides | |
Chang et al. | Lithium‐ion battery: A comprehensive research progress of high nickel ternary cathode material | |
CN110184517B (en) | Porous ternary magnesium-rich hydrogen production hydrolysis alloy and preparation method thereof | |
CN109346766A (en) | A kind of NASICON type lithium ion solid electrolyte, preparation method and applications | |
CN106702191B (en) | A kind of ferrotianium yttrium base hydrogen storage material and intermediate alloy and preparation method | |
Yin et al. | A comparative study of NbF5 catalytic effects on hydrogenation/dehydrogenation kinetics of Mg-Zn-Ni and Mg-Cu-Ni systems | |
CN107523735A (en) | Add Co and Y TiFe hydrogen bearing alloys and preparation method thereof | |
CN102583241A (en) | Sodium borohydride matrix composite used for generating hydrogen by hydrolysis | |
Yin et al. | Ni-based catalyst assisted by MnO to boost the hydrogen storage performance of magnesium hydride | |
Hou et al. | Outstanding hydrogen production properties of surface catalysts promoted Mg–Ni–Ce composites at room temperature in simulated seawater | |
CN109852847A (en) | Al-Ga-In-Sn-Cu alloy of hydrogen manufacturing and preparation method thereof, application in a fuel cell | |
CN103879959B (en) | The aluminum-based composite hydrogen manufacturing material of a kind of high unit hydrogen output and Synthesis and applications thereof | |
CN102618761A (en) | Magnesium-based hydrogen storage alloy material and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Open date: 20091230 |