Hydrogen storage magnesium alloy and preparation method thereof

文档序号：389241 发布日期：2021-12-14 浏览：10次中文

阅读说明：本技术 一种储氢镁合金及其制备方法 (Hydrogen storage magnesium alloy and preparation method thereof ) 是由付彭怀徐雯钰朱荣玉肖刚彭立明丁文江于 2021-08-24 设计创作，主要内容包括：本发明公开了一种储氢镁合金及其制备方法,所述镁合金的组分及其质量百分比为：10.0～20.0％Ni,0.02～0.3％Cu,常规杂质元素含量小于0.2％,余量为Mg；所述制备方法包括大气环境下镁合金熔配和铸造成型两个工序。本发明通过微量Cu元素的添加改变了镁镍合金Mg-(2)Ni相的形貌、提高了镁镍合金的储氢能力,与现有Mg-Ni-Na储氢镁合金相比,本发明中提供的Mg-Ni-Cu储氢镁合金能够在大气环境下批量生产,更有利于镁镍基储氢合金的推广应用。(The invention discloses a hydrogen storage magnesium alloy and a preparation method thereof, wherein the magnesium alloy comprises the following components in percentage by mass: 10.0-20.0% of Ni, 0.02-0.3% of Cu, less than 0.2% of conventional impurity elements and the balance of Mg; the preparation method comprises two working procedures of magnesium alloy melting and matching and casting forming in atmospheric environment. The invention changes Mg-Ni alloy Mg by adding trace Cu element 2 The shape of the Ni phase improves the hydrogen storage capacity of the magnesium-nickel alloy, and compared with the existing Mg-Ni-Na hydrogen storage magnesium alloy, the Mg-Ni-Cu hydrogen storage magnesium alloy provided by the invention can be produced in batches in the atmospheric environment, thereby being more beneficial to popularization and application of the magnesium-nickel base hydrogen storage alloy.)

1. The hydrogen storage magnesium alloy is characterized by comprising the following components in percentage by mass: 10.0-20.0% of Ni, 0.02-0.3% of Cu, and the balance of magnesium and inevitable impurities, wherein the sum of the mass percentages of the impurities is not more than 0.2%.

2. A method for producing a hydrogen occluding magnesium alloy as recited in claim 1, comprising the steps of:

A. melting and preparing the magnesium alloy: melting preheated pure magnesium in a protective atmosphere, and adding preheated pure nickel and pure copper when a melt is heated to 700-740 ℃ after the pure magnesium is melted; after the pure nickel and the pure copper are melted, stirring and cleaning the surface of the melt, and then standing the magnesium alloy melt at 720-740 ℃;

B. casting and forming: and standing the magnesium alloy melt for 10-30 minutes, and then pouring to obtain the hydrogen storage magnesium alloy ingot.

3. The method for producing a hydrogen-storing magnesium alloy as recited in claim 2, wherein in the step A, the atmosphere for protection is SF₆And CO₂Of mixed gas of (1), wherein SF₆The volume content is 0.1-1%.

4. The method for producing a hydrogen occluding magnesium alloy as recited in claim 2, wherein in the step A, the preheating conditions of pure magnesium, pure nickel and pure copper are as follows: preheating at 200 deg.C for more than 3 hr.

5. The method for producing a hydrogen occluding magnesium alloy as recited in claim 2, wherein the casting in the step B is performed by using a magnesium alloy transfer pump and the casting is completed within 2 hours.

6. The method for producing a hydrogen occluding magnesium alloy as recited in claim 5, wherein the casting temperature of the magnesium alloy melt in the step B is controlled to 660 to 680 ℃.

7. The method for producing a hydrogen occluding magnesium alloy as recited in claim 2, wherein the step A further comprises a sodium salt modification step.

8. The method for producing a hydrogen-storing magnesium alloy according to claim 7, wherein the sodium salt modification step is: after the pure nickel and the pure copper are melted, the obtained Mg-Ni-Cu alloy melt is stirred and uniformly sprinkled with low-melting-point sodium salt on the surface of the magnesium alloy melt under the protective atmosphere, and the sodium salt melt is fully reacted with the magnesium alloy melt through stirring.

9. The method for producing a hydrogen-storing magnesium alloy as recited in claim 8, wherein the low-melting-point sodium salt is composed of NaF, NaCl, KCl in a mass ratio of 30%, 40% and 30%, respectively.

10. The method for producing a hydrogen-storing magnesium alloy as claimed in claim 9, wherein the amount of the low-melting-point sodium salt added is 1.0 to 2.0% by mass of the melt of the Mg-Ni-Cu alloy.

Technical Field

The invention belongs to the field of metal material processing, and particularly relates to a hydrogen storage magnesium alloy and a preparation method thereof.

Background

Energy sources are the material basis for human existence and continued development. Because traditional energy sources such as coal, petroleum, natural gas and the like can not be regenerated, alternative energy sources such as solar energy, wind energy, geothermal energy, hydrogen energy and the like are continuously developed under the attention of human beings, wherein the hydrogen energy is one of the well-known future energy sources with the optimal prospect. The hydrogen storage in the form of metal compound is one of the best hydrogen storage schemes so far, and has the characteristics of large hydrogen storage capacity, good hydrogen absorption and desorption thermodynamics, high hydrogen desorption purity, high safety and the like. When hydrogen absorption is required, the metal reacts with hydrogen to form a hydride, thereby storing the hydrogen; when hydrogen release is needed, the metal hydride releases hydrogen by controlling the temperature and/or the pressure; both hydrogen absorption and hydrogen desorption are simple and easy reversible processes. Among many metals, pure magnesium has a hydrogen storage amount of up to 7.6 wt%, and is the metal material with the highest energy storage among practical reversible hydrogen storage materials, and meanwhile, magnesium resources are abundant, so that magnesium-based hydrogen storage materials become research hotspots of hydrogen storage materials and have great development potential.

Mg-Ni alloys having a large amount of Mg/Mg₂Ni phase boundary, phase boundary conversion of Mg to MgH₂Has good catalysis, so that the Mg-Ni alloy shows good hydrogen absorption and desorption effects and becomes a hotspot of research and application. CN101120111A magnesium alloy for hydrogen storage discloses a magnesium alloy for hydrogen storage and a manufacturing method thereof, the magnesium alloy for hydrogen storage is formed by introducing one or more of refining elements Zr, Na, K, Ba, Ca, Sr, La, Y, Yb, Rb and Cs on the basis of Mg-Ni alloy, wherein the Mg-Ni-Na alloy has very good hydrogen storage effect: large hydrogen storage capacity and high hydrogen charging and discharging speed. However, since Na is extremely active and is easily burnt out when it is melted in the atmosphere, the melting can be carried out only in a non-oxidizing atmosphere such as vacuum melting, as disclosed in CN101120111AA method for manufacturing the same. Because the quantity of the hydrogen storage magnesium alloy which can be prepared at one time by vacuum melting is limited, usually less than 50Kg, the production efficiency of the hydrogen storage magnesium alloy is low, the production cost is higher, and the large-scale application of the hydrogen storage magnesium alloy is limited.

Disclosure of Invention

In order to break through the industrial problems that the existing high-capacity Mg-Ni-Na hydrogen storage magnesium alloy cannot be manufactured in large scale at low cost, the invention provides the hydrogen storage magnesium alloy and the preparation method thereof, and the hydrogen storage magnesium alloy can be produced in large scale in the atmospheric environment.

The purpose of the invention is realized by the following technical scheme:

in a first aspect, the invention provides a hydrogen storage magnesium alloy, comprising the following components by mass percent: 10.0-20.0% of Ni, 0.02-0.3% of Cu, and the balance of magnesium and inevitable impurities, wherein the sum of the mass percentages of the impurities is not more than 0.2%.

The invention adopts Ni (nickel) as a first component: the existing research shows that when the Ni content in the Mg-Ni alloy is between 10.0 and 20.0 percent, the alloy has good hydrogen absorption and desorption effects.

The invention adopts Cu (copper) as a second component: the research shows that the addition of trace Cu element can obviously change Mg₂The morphology of the Ni phase improves the hydrogen absorption and desorption kinetics of the Mg-Ni alloy, and the Cu element can promote the decomposition of hydrogen into hydrogen atoms and promote the formation of metal hydride.

In a second aspect, the present invention provides a method for preparing a hydrogen storage magnesium alloy, comprising the steps of:

B. casting and forming: and standing the magnesium alloy melt for 10-30 minutes, and then pouring to obtain the hydrogen storage magnesium alloy ingot.

Preferably, in step A, the protective atmosphere is SF₆And CO₂Of mixed gas of (1), wherein SF₆The volume content is 0.1-1%.

Preferably, in step a, the preheating conditions of pure magnesium, pure nickel and pure copper are as follows: preheating at 200 deg.C for more than 3 hr.

Preferably, the magnesium alloy liquid transfer pump is adopted for pouring in the step B, and the pouring is completed within 2 hours.

Preferably, the casting temperature of the magnesium alloy melt in the step B is controlled to be 660-680 ℃.

According to the invention, the magnesium alloy liquid transfer pump is used for melt pouring, so that the pouring efficiency is improved, and compared with the conventional pouring ladle pouring, the specific gravity segregation of nickel elements can be effectively reduced: the magnesium alloy liquid transfer pump can effectively stir the melt in the melt when the magnesium alloy melt is poured, and the stirring can effectively reduce the specific gravity segregation caused by the large specific gravity of the nickel element in the casting process.

Preferably, step a further comprises a sodium salt modification step.

Preferably, the sodium salt modification step is: after the pure nickel and the pure copper are melted, the obtained Mg-Ni-Cu alloy melt is stirred and uniformly sprinkled with low-melting-point sodium salt on the surface of the magnesium alloy melt under the protective atmosphere, and the sodium salt melt is fully reacted with the magnesium alloy melt through stirring.

Preferably, the low-melting-point sodium salt consists of NaF, NaCl and KCl in a mass percentage of 30%, 40% and 30% respectively.

Preferably, the addition amount of the low-melting-point sodium salt is 1.0-2.0% of the mass of the Mg-Ni-Cu alloy melt.

Compared with the prior art, the invention has the following beneficial effects:

(1) the main alloy elements of the hydrogen storage magnesium alloy are Ni and Cu, both elements are inert metals, and the hydrogen storage magnesium alloy is not easy to burn when smelted in the atmosphere, and is more convenient for the alloy to be smelted in the atmosphere environment compared with the prior high-capacity Mg-Ni-Na hydrogen storage magnesium alloy patent technology; meanwhile, the prepared Mg-Ni-Cu alloy has higher hydrogen storage capacity.

(2) In the invention, the addition of trace Cu element obviously changes Mg₂The morphology of the Ni phase obviously enhances the hydrogen absorption and desorption capacity of the Mg-Ni alloy: compared with Mg-15Ni alloy, the hydrogen absorption capacity of the alloy after 8 hours of hydrogen filling is increased by 7.5 percent by adding trace Cu element.

(3) When sodium salt is adopted for modification, sodium ions and pure magnesium are subjected to chemical reaction in the modification process to generate sodium atoms, the sodium atoms are uniformly distributed in the alloy melt, and the sodium atoms are uniformly distributed in Mg and Mg in the solidification process of the alloy melt₂At the interface of Ni phase, refining Mg₂And meanwhile, the Ni phase can effectively improve the response rate of the subsequent hydrogen charging and discharging of the alloy, and the hydrogen absorption and discharge dynamics of the Mg-Ni alloy are improved. Compared with the mode of obtaining the sodium element by adding the metallic sodium in the prior Mg-Ni-Na hydrogen storage magnesium alloy technology, the method for adding the sodium element by the low-melting-point sodium salt is simple and easy to implement, can obviously reduce the potential safety hazard of the metallic sodium in purchasing, using and storing, and simultaneously obviously reduces the production cost.

(4) The Mg-Ni-Cu hydrogen storage alloy ingot prepared by the invention can obtain fine powder through processes of cutting, crushing and the like, and the powder can store hydrogen after being pressed and formed, and has good hydrogen charging and discharging effects, thereby greatly simplifying the preparation process of the high-capacity Mg-Ni-Na hydrogen storage material, remarkably reducing the manufacturing cost of the hydrogen storage magnesium alloy, being convenient for mass production of the hydrogen storage magnesium alloy with low cost, and promoting the application of the hydrogen storage magnesium alloy.

Drawings

Other features, objects and advantages of the invention will become more apparent upon reading of the detailed description of non-limiting embodiments with reference to the following drawings:

FIG. 1 shows the difference of microstructure of Mg-15Ni alloy with or without trace Cu element addition: FIG. 1(a) is a Mg-15Ni alloy of comparative example 1, in which Mg₂The Ni phase is in a short rod shape and a strip shape; FIG. 1(b) is an alloy of Mg-15Ni-0.1Cu in example 1, in which Mg₂The Ni phase is in a lamellar shape; FIG. 1(a) and FIG. 1(b) are the same magnification of the microstructure;

FIG. 2 is a graph showing hydrogen absorption curves of the Mg-15Ni alloy in comparative example 1 and the Mg-15Ni-0.1Cu alloy in example 1: the addition of a small amount of Cu element obviously increases the hydrogen absorption amount of the alloy;

FIG. 3 is a graph of hydrogen absorption curves for a low melting point sodium salt deteriorated and non-deteriorated Mg-15Ni-0.1Cu alloy, wherein the sample without sodium salt deterioration is from example 1 and the sample with sodium salt deterioration is from example 6; the hydrogen absorption kinetics of the Mg-15Ni-0.1Cu alloy after the sodium salt is modified is remarkably improved: the hydrogen absorption time is 2h, the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy prepared by the conventional method in the example 1 is 4.47 percent, and the hydrogen absorption amount of the alloy modified by the sodium salt in the example 6 is 4.98 percent and is increased by 11.4 percent; and hydrogen is absorbed for 4 hours, the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy prepared by the conventional method is 5.39%, and the hydrogen absorption amount of the alloy after the sodium salt is modified is 5.63%, which is improved by 4.5%.

Detailed Description

The present invention will be described in detail with reference to specific examples. The following examples will assist those skilled in the art in further understanding the invention, but are not intended to limit the invention in any way. It should be noted that variations and modifications can be made by persons skilled in the art without departing from the spirit of the invention. All falling within the scope of the present invention.

Example 1

In this example, 300kg of Mg-15Ni-0.1Cu hydrogen storage magnesium alloy was prepared in a single step by using the hydrogen storage magnesium alloy and the preparation method thereof. The specific method comprises the following steps:

step A: and (4) melting and matching the magnesium alloy.

Preheating 45Kg of pure nickel sheet (15 wt%) and 0.3Kg of pure copper sheet (0.1 wt%) at 200 ℃ for 3h respectively in an atmospheric environment; 255Kg of pure magnesium was placed in a 300Kg crucible with 0.1% SF₆And 99.9% CO₂Melting the mixture in the atmosphere of the mixed gas, and adding preheated pure nickel sheets and pure copper sheets when the melt is heated to 700-740 ℃ after the pure magnesium is melted; after the pure nickel and the pure copper are melted, stirring the magnesium alloy melt to enable nickel and copper elements to be uniformly distributed, then cleaning the surface of the melt, and standing the magnesium alloy melt at 720-740 ℃.

And B: and (5) casting and forming.

Standing the Mg-Ni-Cu alloy melt for 20 minutes, and then using a magnesium alloy liquid transfer pump for 60 minutesCasting the magnesium alloy melt into an ingot (the casting temperature is 660-670 ℃) in a clock, positioning a material taking port of a liquid transfer pump at the middle lower part of a crucible, and adopting 0.1% SF in the casting process₆And 99.9% CO₂The mixed gas is used for protection, and a plurality of hydrogen storage magnesium alloy ingots with single ingots of 5.0Kg are obtained. The ingot is cut and crushed subsequently to obtain the hydrogen storage magnesium alloy powder. The microstructure of the Mg-15Ni-0.1Cu alloy obtained in this example is shown in FIG. 1(b), in which Mg is present₂The Ni phase is lamellar.

Example 2

In the embodiment, 800kg of Mg-15Ni-0.1Cu hydrogen storage magnesium alloy is prepared by adopting the hydrogen storage magnesium alloy and the preparation method thereof. The specific method comprises the following steps:

step A: and (4) melting and matching the magnesium alloy.

Preheating 120Kg of pure nickel sheet (15 wt%) and 0.8Kg of pure copper sheet (0.1%) at 200 ℃ for 3h respectively in an atmospheric environment; 680Kg of pure magnesium was placed in a 800Kg crucible with 0.1% SF₆And 99.9% CO₂Melting the mixture in the atmosphere of the mixed gas, and adding preheated pure nickel sheets and pure copper sheets when the melt is heated to 700-740 ℃ after the pure magnesium is melted; after the pure nickel and the pure copper are melted, stirring the magnesium alloy melt to enable nickel and copper elements to be uniformly distributed, then cleaning the surface of the melt, and standing the magnesium alloy melt at 720-740 ℃.

And B: and (5) casting and forming.

After the Mg-Ni-Cu alloy melt is kept stand for 20 minutes, the magnesium alloy melt is cast into an ingot within 120 minutes by a magnesium alloy liquid transfer pump (the casting temperature is670-680 ℃), wherein a material taking port of the liquid transferring pump is positioned at the middle lower part of the crucible, and 0.1% SF is adopted in the pouring process₆And 99.9% CO₂The mixed gas is used for protection, and a plurality of hydrogen storage magnesium alloy ingots with single ingots of 5.0Kg are obtained. The ingot is cut and crushed subsequently to obtain the hydrogen storage magnesium alloy powder.

Example 3

This example is essentially the same as example 1, except that: the Cu element content adopted in this example was 0.05 wt%, and a Mg-15Ni-0.05Cu alloy ingot was obtained.

Example 4

This example is essentially the same as example 1, but differs therefrom only in that: the content of the Cu element used in this example was 0.2 wt%, and a Mg-15Ni-0.2Cu alloy ingot was obtained.

Example 5

This example is essentially the same as example 1, but differs therefrom only in that: the content of the Cu element used in this example was 0.3 wt%, and a Mg-15Ni-0.3Cu alloy ingot was obtained.

Example 6

This example is essentially the same as example 1, but differs therefrom only in that: a sodium salt modification procedure is added in the step A: after pure nickel and pure copper are melted, uniformly spraying low-melting-point sodium salt on the surface of the magnesium alloy melt under the protective atmosphere by stirring, wherein the low-melting-point sodium salt consists of 30 wt% of NaF, 40 wt% of NaCl and 30 wt% of KCl, and the addition amount is 1.0 wt% of the mass of the melt, namely 3.0 Kg. The low-melting-point sodium salt is changed into liquid under the action of the magnesium alloy melt at high temperature, and the sodium salt melt and the magnesium alloy melt are fully reacted by stirring. And casting to obtain the Mg-15Ni-0.1Cu-Na alloy cast ingot with the modified sodium salt.

Selecting the magnesium alloy hydrogen storage ingot cast finally to be cut, crushed and granulated by the conventional methodDiameter of a pipe<80-mesh fine powder, and pressing the fine powderThe cylinder sample was subjected to a hydrogen storage capacity test. After charging hydrogen for 8 hours at 340 ℃ under the initial pressure of 3.1MPa, the average hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by the sodium salt reaches 6.29 wt%, compared with the Mg-15Ni-0.1Cu alloy not modified by the sodium salt (the average hydrogen absorption amount is 6.29 wt%, example 1), the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by the sodium salt after charging hydrogen for 8 hours is equivalent, but the hydrogen absorption response rate is obviously improved: as shown in FIG. 3, the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy (i.e., the result of the conventional casting in FIG. 3, example 1) was 4.47% for 2 hours, while the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified with sodium salt (i.e., the result of the modification of sodium salt in FIG. 3) was 4.98%, which was increased by 11.4%; the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy is 5.39 percent after absorbing hydrogen for 4 hours, and the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by sodium salt is 5.63 percent, which is improved by 4.5 percent.

Example 7

This example is essentially the same as example 6, but differs therefrom only in that: the addition of the low-melting-point sodium salt adopted in the embodiment is 2.0 wt% of the melt mass, namely 6.0Kg, and the Mg-15Ni-0.1Cu-Na alloy ingot is obtained.

Selecting the magnesium alloy hydrogen storage ingot cast last to be cast, and crushing the magnesium alloy hydrogen storage ingot into particle size by conventional cutting<80-mesh fine powder, and pressing the fine powderThe cylinder sample was subjected to a hydrogen storage capacity test. Under the initial pressure of 3.1MPa and after being charged with hydrogen for 8 hours at the temperature of 340 ℃, the average hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy reaches 6.25 wt%, compared with the Mg-15Ni-0.1Cu alloy which is not modified by sodium salt (the average hydrogen absorption amount is 6.29 wt%), the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by sodium salt after being charged with hydrogen for 8 hours is slightly reduced, but the hydrogen absorption response rate is obviously improved: the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy is 4.47 percent after absorbing hydrogen for 2 hours, and the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by sodium salt is 4.94 percent, which is improved by 10.5 percent; absorbing hydrogenThe hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy is 5.39% in 4 hours, while the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by sodium salt is 5.61%, which is improved by 4.1%.

Comparative example 1

This comparative example was prepared essentially the same as example 1, except that: the comparative example does not add Cu element, and only obtains Mg-15Ni alloy cast ingot. The microstructure of the Mg-15Ni alloy obtained in this comparative example is shown in FIG. 1(a), in which Mg is present₂The Ni phase is in the shape of short rod and long strip.

Comparative example 2

This example is essentially the same as example 1, but differs therefrom only in that: the comparative example added Cu element content was 0.4 wt%, and Mg-15Ni-0.4Cu alloy ingot was obtained.

Comparative example 3

This comparative example was prepared essentially the same as example 6, except that: the comparative example does not add Cu element, and only obtains Mg-15Ni-Na alloy cast ingot.

Comparative example 4

This comparative example was prepared essentially the same as example 1, except that: in the comparative example, the Mg-15Ni-0.1Zn alloy cast ingot is obtained by adding 0.1Zn element instead of Cu element.

Comparative example 5

This comparative example was prepared essentially the same as example 6, except that: the addition of the low-melting-point sodium salt adopted in the embodiment is 0.5 wt% of the mass of the melt, namely 1.5Kg, and the Mg-15Ni-0.1Cu-Na alloy ingot is obtained.

Selecting the magnesium alloy hydrogen storage ingot cast last to be cast, and crushing the magnesium alloy hydrogen storage ingot into particle size by conventional cutting<80-mesh fine powder, and pressing the fine powderPerforming hydrogen storage on the cylindrical sampleAnd (5) testing the capability. The average hydrogen absorption of the Mg-15Ni-0.1Cu-Na alloy prepared in this comparative example was 5.96 wt% after charging hydrogen at 340 ℃ for 8 hours under an initial pressure of 3.1MPa, which is significantly lower than that of the Mg-15Ni-0.1Cu alloy that had not undergone sodium salt deterioration (average hydrogen absorption was 6.29 wt%, example 1). The alloy hydrogen absorption response rate is obviously improved: the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy is 4.47 percent after absorbing hydrogen for 2 hours, while the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by sodium salt in the comparative example is 4.92 percent, which is improved by 10.1 percent; the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy after hydrogen absorption for 4 hours was 5.39%, while the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy subjected to sodium salt modification of the present comparative example was 5.56%, which was improved by 3.2%.

Comparative example 6

This comparative example was prepared essentially the same as example 6, except that: the addition of the low-melting-point sodium salt adopted in the embodiment is 2.5 wt% of the melt mass, namely 7.5Kg, and the Mg-15Ni-0.1Cu-Na alloy ingot is obtained.

Selecting the magnesium alloy hydrogen storage ingot cast last to be cast, and crushing the magnesium alloy hydrogen storage ingot into particle size by conventional cutting<80-mesh fine powder, and pressing the fine powderThe cylinder sample was subjected to a hydrogen storage capacity test. The average hydrogen absorption of the Mg-15Ni-0.1Cu-Na alloy prepared in this comparative example was 5.99 wt% after charging hydrogen at 340 ℃ for 8 hours under an initial pressure of 3.1MPa, which is significantly lower than that of the Mg-15Ni-0.1Cu alloy that had not undergone sodium salt deterioration (average hydrogen absorption was 6.29 wt%, example 1). The alloy hydrogen absorption response rate is obviously improved: the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy is 4.47 percent after absorbing hydrogen for 2 hours, while the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy modified by the sodium salt of the comparative example is 4.90 percent, which is improved by 9.6 percent; the hydrogen absorption amount of the Mg-15Ni-0.1Cu alloy after absorbing hydrogen for 4 hours was 5.39%, while the hydrogen absorption amount of the Mg-15Ni-0.1Cu-Na alloy subjected to the modification of the sodium salt of this comparative example was 5.54%, which was improved by 2.8%.

In conclusion, the invention changes Mg-Ni alloy Mg by introducing trace Cu element₂The shape of Ni phase improves the hydrogen storage capacity of the magnesium-nickel alloy, and compared with the existing Mg-Ni-Na hydrogen storage magnesium alloy, the magnesium-nickel alloy has the advantages thatThe Mg-Ni-Cu hydrogen storage magnesium alloy provided by the invention can be produced in batches in the atmospheric environment, and is more beneficial to popularization and application of the magnesium-nickel base hydrogen storage alloy.

The invention has many applications, and the above description is only a preferred embodiment of the invention. It should be noted that the above examples are only for illustrating the present invention, and are not intended to limit the scope of the present invention. It will be apparent to those skilled in the art that various modifications can be made without departing from the principles of the invention and these modifications are to be considered within the scope of the invention.

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