CN104862514A - Surface modifying method of AB3 type hydrogen storage alloy - Google Patents
Surface modifying method of AB3 type hydrogen storage alloy Download PDFInfo
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- CN104862514A CN104862514A CN201510249890.4A CN201510249890A CN104862514A CN 104862514 A CN104862514 A CN 104862514A CN 201510249890 A CN201510249890 A CN 201510249890A CN 104862514 A CN104862514 A CN 104862514A
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- hydrogen storage
- alloy
- storage alloy
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Abstract
The invention discloses a surface modifying method of AB3 type hydrogen storage alloy. AB3 type Mm0.78Mg0.22Ni2.48Mn0.09Al0.23Co0.47 parent alloy is prepared through a vacuum induction melting method, and after an alloy ingot is mechanically smashed, particle powder of 200-300 meshes is screened out through ball milling; 95-99% of Mm0.78Mg0.22Ni2.48Mn0.09Al0.23Co0.47 and 1-5% of grapheme are mixed evenly, then ball milling is carried out, and accordingly the AB3 type hydrogen storage alloy with the surface modified is prepared. The method is easy to operate and popularize on a large scale, and the modified AB3 type hydrogen storage alloy can be used for manufacturing hydrogen storage alloy electrodes with good electrochemistry performance.
Description
Technical field
The invention belongs to materials chemistry and electrochemical research field, particularly Graphene is to AB
3type Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47(Mm is mishmetal, and the weight percent of composition is: 82.3% La and 17.7% Nd) hydrogen storage alloy carries out the method for surface modification.
Background technology
Current business-like Ni/MH cell negative electrode material mainly uses AB
5type hydrogen storage alloy, but its specific storage is close to theoretical value, be difficult to improve its capacity again, and electric bicycle, electromobile and hybrid electric vehicle on market etc. need high specific storage, high-power, are therefore badly in need of exploitation new heavy body, more powerful Ni/MH cell negative electrode material.AB
3type hydrogen storage alloy has relatively high loading capacity, and thus application prospect is good, but its surface is oxidizable, perishable, cyclical stability is poor, makes it be restricted in practical application.Relevant Graphene is to AB at present
3the research of type alloy surface modifying is less.
Summary of the invention
The object of this invention is to provide a kind of AB
3the surface modifying method of type hydrogen storage alloy.
Thinking of the present invention: using conductive graphene as properties-correcting agent, with AB
3type alloy prepares Mm by ball milling
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47/ Graphene modified alloy, forms the protective membrane of one deck densification at alloy surface, slow down the corrosion oxidation of alkali lye alloy, simultaneously by the fixed action of Graphene alloy powder, suppresses the efflorescence speed of alloy, reaches and improve AB
3the object of type alloy electrode chemical property.
Concrete steps are:
(1) AB is prepared by vacuum induction melting method
3type Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47precursor alloy, after alloy pig mechanical disintegration, with rotating speed 250 ~ 300 revs/min of ball millings 60 ~ 90 minutes, sieves out 200 ~ 300 object Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder; Described Mm is mishmetal, and the weight percent of its composition is: 82.3% La and 17.7% Nd.
(2) by Mm obtained for step (1)
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder and Graphene mix according to following weight percent: Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder is 95 ~ 99%, and Graphene is 1 ~ 5%, and sum of the two is 100%; Carry out ball milling after mixing, drum's speed of rotation is 200 ~ 250 revs/min, and Ball-milling Time is 30 ~ 60 minutes, i.e. the AB of obtained surface modification
3type hydrogen storage alloy.
The inventive method is simple to operate, is easy to large-scale promotion, and modified AB
3type hydrogen storage alloy can prepare the hydrogen-bearing alloy electrode having good electrical chemical property.
Embodiment
embodiment 1:
(1) AB is prepared by vacuum induction melting method
3type Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47precursor alloy, after alloy pig mechanical disintegration, with rotating speed 300 revs/min of ball millings 60 minutes, sieves out 300 object Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder; Described Mm is mishmetal, and the weight percent of its composition is: 82.3% La and 17.7% Nd.
(2) by Mm obtained for step (1)
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder and Graphene mix according to following weight percent: Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder is 99%, and Graphene is 1%, and sum of the two is 100%; Carry out ball milling after mixing, drum's speed of rotation is 200 revs/min, and Ball-milling Time is 30 minutes, i.e. the AB of obtained surface modification
3type hydrogen storage alloy.
embodiment 2:
In step (2), raw material weight per-cent changes into: Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder be 98% and Graphene be 2%, all the other are with embodiment 1.
embodiment 3:
In step (2), raw material weight per-cent changes into: Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder be 95% and Graphene be 5%, all the other are with embodiment 1.
Measure with LAND 5.3B battery test system and CHI 660E electrochemical workstation cyclical stability and the dynamic performance that the present embodiment obtains modified alloy respectively, result is as follows:
1) alloy electrode is at interpolation Graphene after milled processed, along with the increase of Graphene consumption, maximum discharge capacity is first increased to 364.9 mAh/g (Graphene consumption is 2%) from 292.0 m Ah/g (not graphene-containing), then drops to again 364.9 mAh/g (Graphene consumption is 5%).
2), after adding Graphene, exchange current density, the limit current density of electrode all present the trend first increasing and reduce afterwards.In studied electrode, when Graphene consumption is 2%, electrode has best comprehensive electrochemical.
Above-mentioned result of study confirms, ball milling does not change the structure of precursor alloy, and modified alloy is by LaNi
5phase and La
2ni
7phase composite, and Graphene is as surface-modifying agent, can not only improve AB
3type Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47the loading capacity of alloy electrode, can also improve the kinetic property of electrode.
Claims (1)
1. an AB
3the surface modifying method of type hydrogen storage alloy, is characterized in that concrete steps are:
(1) AB is prepared by vacuum induction melting method
3type Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47precursor alloy, after alloy pig mechanical disintegration, with rotating speed 250 ~ 300 revs/min of ball millings 60 ~ 90 minutes, sieves out 200 ~ 300 object Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder; Described Mm is mishmetal, and the weight percent of its composition is: 82.3% La and 17.7% Nd;
(2) by Mm obtained for step (1)
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder and Graphene mix according to following weight percent: Mm
0.78mg
0.22ni
2.48mn
0.09al
0.23co
0.47alloying pellet powder is 95 ~ 99%, and Graphene is 1 ~ 5%, and sum of the two is 100%; Carry out ball milling after mixing, drum's speed of rotation is 200 ~ 250 revs/min, and Ball-milling Time is 30 ~ 60 minutes, i.e. the AB of obtained surface modification
3type hydrogen storage alloy.
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CN201510249890.4A CN104862514A (en) | 2015-05-17 | 2015-05-17 | Surface modifying method of AB3 type hydrogen storage alloy |
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Publication Number | Publication Date |
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Family
ID=53908677
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106001543A (en) * | 2016-06-09 | 2016-10-12 | 桂林理工大学 | Method for modifying La-Mg-Ni based hydrogen storage alloy by utilizing Ni-B-C alloy |
CN106041048A (en) * | 2016-07-21 | 2016-10-26 | 桂林理工大学 | Method for carrying out surface modification on an AB3-type hydrogen storage alloy by utilizing cobalt phthalocyanine |
CN106784705A (en) * | 2016-12-27 | 2017-05-31 | 中科泰能高铭科技发展有限公司 | A kind of hydrogen storing alloy powder and its surface treatment method |
CN108456794A (en) * | 2018-03-31 | 2018-08-28 | 桂林理工大学 | It is a kind of to be modified AB using polypyrrole3The method of type hydrogen storage alloy |
CN108539155A (en) * | 2018-03-31 | 2018-09-14 | 桂林理工大学 | It is a kind of to be modified AB using polyparaphenylene3The method of type hydrogen storage alloy |
CN110788329A (en) * | 2019-11-07 | 2020-02-14 | 江苏集萃安泰创明先进能源材料研究院有限公司 | Carbon-containing composite hydrogen storage alloy and preparation method thereof, composite solid hydrogen storage tank and hydrogen storage performance testing method |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070144063A1 (en) * | 2005-12-21 | 2007-06-28 | The Penn State Research Foundation | Synthesis of hydrogen-carbon clathrate material and hydrogen evolution therefrom at moderate temperatures and pressures |
JP2012087011A (en) * | 2010-10-20 | 2012-05-10 | Kri Inc | Graphite nano-ribbon, and method for manufacturing the same |
CN102618754A (en) * | 2012-03-22 | 2012-08-01 | 桂林理工大学 | Preparation method of AB3-AB5 composite alloy |
CN103611930A (en) * | 2013-12-19 | 2014-03-05 | 桂林理工大学 | Method for surface modification of AB3 type hydrogen storage alloy |
CN104226985A (en) * | 2014-06-29 | 2014-12-24 | 桂林理工大学 | Nickel plating modification method for AB3 type hydrogen storage alloy |
-
2015
- 2015-05-17 CN CN201510249890.4A patent/CN104862514A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070144063A1 (en) * | 2005-12-21 | 2007-06-28 | The Penn State Research Foundation | Synthesis of hydrogen-carbon clathrate material and hydrogen evolution therefrom at moderate temperatures and pressures |
JP2012087011A (en) * | 2010-10-20 | 2012-05-10 | Kri Inc | Graphite nano-ribbon, and method for manufacturing the same |
CN102618754A (en) * | 2012-03-22 | 2012-08-01 | 桂林理工大学 | Preparation method of AB3-AB5 composite alloy |
CN103611930A (en) * | 2013-12-19 | 2014-03-05 | 桂林理工大学 | Method for surface modification of AB3 type hydrogen storage alloy |
CN104226985A (en) * | 2014-06-29 | 2014-12-24 | 桂林理工大学 | Nickel plating modification method for AB3 type hydrogen storage alloy |
Non-Patent Citations (4)
Title |
---|
ANBAO YUAN,ET,AL: "A study on the effect of nickel,cobalt or graphite addition on the electrochemical properties of an AB5 hydrogen storage alloy and the mechanism of the effects", 《JOURNAL OF ALLOYS AND COMPOUNDS》 * |
XIAOFENG LI,ET,AL: "Electrochemical hydrogen absorbing properties of graphite/AB5 alloy", 《JOURNAL OF ALLOYS AND COMPOUNDS》 * |
孙宝龙等: "MgH2-graphene复合储氢材料吸放氢性能", 《安徽工业大学学报》 * |
李玲玲: "镍氢电池负极材料介质阻挡放电等离子球磨制备及改性", 《中国优秀硕士学位论文全文数据库》 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106001543A (en) * | 2016-06-09 | 2016-10-12 | 桂林理工大学 | Method for modifying La-Mg-Ni based hydrogen storage alloy by utilizing Ni-B-C alloy |
CN106041048A (en) * | 2016-07-21 | 2016-10-26 | 桂林理工大学 | Method for carrying out surface modification on an AB3-type hydrogen storage alloy by utilizing cobalt phthalocyanine |
CN106784705A (en) * | 2016-12-27 | 2017-05-31 | 中科泰能高铭科技发展有限公司 | A kind of hydrogen storing alloy powder and its surface treatment method |
CN106784705B (en) * | 2016-12-27 | 2017-10-31 | 中科泰能高铭科技发展有限公司 | A kind of hydrogen storing alloy powder and its surface treatment method |
CN108456794A (en) * | 2018-03-31 | 2018-08-28 | 桂林理工大学 | It is a kind of to be modified AB using polypyrrole3The method of type hydrogen storage alloy |
CN108539155A (en) * | 2018-03-31 | 2018-09-14 | 桂林理工大学 | It is a kind of to be modified AB using polyparaphenylene3The method of type hydrogen storage alloy |
CN110788329A (en) * | 2019-11-07 | 2020-02-14 | 江苏集萃安泰创明先进能源材料研究院有限公司 | Carbon-containing composite hydrogen storage alloy and preparation method thereof, composite solid hydrogen storage tank and hydrogen storage performance testing method |
CN110788329B (en) * | 2019-11-07 | 2022-11-04 | 江苏集萃安泰创明先进能源材料研究院有限公司 | Carbon-containing composite hydrogen storage alloy and preparation method thereof, composite solid hydrogen storage tank and hydrogen storage performance testing method |
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Application publication date: 20150826 |