CN100391589C - Composite hydrogen storage material contg. magnesium-transition metals oxides, prepn. method and application thereof - Google Patents
Composite hydrogen storage material contg. magnesium-transition metals oxides, prepn. method and application thereof Download PDFInfo
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Abstract
A composite hydrogen-bearing material used for the hydrogen fuel battery is prepared from Mg or magnesium hydride powder and the powdered oxide of transition metal through proportional mixing and high-energy ball grinding in H2 or Ar gas for 10-50 hr.
Description
Technical field
The present invention relates to hydrogen storage material, particularly a kind of magnesium-transition metals oxides composite hydrogen storage material and its production and application.
Technical background
Energy development and environmental protection have become the strategic core of human social, and petering out of fossil energy forces people to seek reproducible clean energy resource.Hydrogen Energy is because cleaning, efficient, renewable is acknowledged as the most potential secondary energy sources of 21 century.At present, progressively applying, but its extensive use need solve three subject matters such as practical fields such as automobiles with the fuel cell that hydrogen acts as a fuel, promptly the economy of hydrogen produce, safety in transportation and storage and efficient the use.Wherein the safe and efficient accumulating of hydrogen is a bottleneck of hydrogen energy system development.At present, people still adopt with high-pressure cylinder hydrogen gas storage and the liquid hydrogen hydrogen source as hydrogen fuel cell.These two kinds of methods all exist potential safety hazard, and store the hydrogen of same amount, and required volume ratio metal hydride is much bigger.Hydride hydrogen-storing because of being fine and close solid, is the storage hydrogen means of comparison safety, for the safety in transportation and storage and the application of hydrogen opens up a new way.
Up to now, the many metal hydrogen storage materials of research mainly contain: 1. with LaNi
5For the representative rare earth be AB
5The type alloy; 2. with TiFe the AB type hydrogen storage alloy of representative, 3. with ZrV
2Be the AB of representative
2Type Laves phase hydrogen storage alloy; 4. with LaNi
3New A B for representative
3Type hydrogen storage alloy; 5. with Mg
2Ni is the A of representative
2The Type B hydrogen bearing alloy.Although LaNi
5Type and LaNi
3The type alloy has splendid suction hydrogen desorption kinetics performance and lower suction hydrogen discharging temperature, but it inhales hydrogen weight ratio lower (having only about 1.5%); That TiFe is is 1.8-2.2wt%, and activation process is relatively more difficult; Laves is that the alloy activity cycle is long, hydrogen storage content is low mutually, costs an arm and a leg.Mg
2Ni base magnesium base alloy suction hydrogen weight ratio also only be 3.6%.By index (operating pressure 1～10 atmospheric pressure that proposes in recent years about automobile usefulness hydrogen storage material; Reversible hydrogen storage amount 4～5wt.%; Operating temperature 273～373K), hydrogen storage material will satisfy above-mentioned three indexs simultaneously, particularly store up hydrogen weight ratio 4～5% these indexs, remain further to study and explore the novel metal hydrogen storage material.And magnesium becomes a kind of most promising candidate metals hydrogen storage material with high weight of hydrogen (the weight hydrogen storage content is 7.6%), aboundresources, advantage such as cheap, pollution-free.But magnesium is used so far yet in practice owing to suction hydrogen discharging temperature height, dynamic performance are poor.The higher material of a kind of hydrogen storage content is disclosed among the Chinese patent CN1204282C, though improved to a certain extent pure magnesium hydrogen storage material charge and discharge hydrogen dynamics and thermodynamic property, but owing to added the nickel of not inhaling hydrogen, cause its hydrogen to decrease, because nickel is relatively expensive, increased the cost of material simultaneously.
Summary of the invention
The present invention aims to provide a kind of magnesium-transition metals oxides composite hydrogen storage material and its production and application.The present invention is nanometer/amorphous state magnesium-transition metals oxides composite hydrogen storage material, can obviously improve the storage hydrogen dynamic performance of magnesium hydrogen storage material when keeping its high weight of hydrogen, also obviously reduces its hydrogen storage temperature simultaneously.Material of the present invention is suitable for safe, the efficient accumulating, the particularly application on hydrogen fuel cell of hydrogen, is expected to be used for the storage hydrogen carrier of hydrogen fuel cell.
The adding of transition metal oxide can improve the hydrogen storage property of magnesium hydrogen storage material among the present invention.In general the thermodynamic stability of transition metal oxide generally will be lower than MgO, and the oxygen atom of a small amount of transition metal oxide generates MgO with the Mg reaction in mechanical milling process, introduce fault of construction, provides the activated centre for inhaling hydrogen discharge reaction; Secondly, the metal ion of transition metal oxide generally all has a plurality of valence states can be H
2Generation and decomposition provide a part of unoccupied orbital, the generation that helps reacting.These character that transition metal oxide had can obviously be improved the storage hydrogen dynamic performance of magnesium hydrogen storage material, simultaneously because the catalytic performance of transition metal oxide is relatively good, the adding of a small amount of transition metal oxide can obviously improve the performance of magnesium, so its maximum storage hydrogen quantity also is significantly increased.Adopt ball-milling method that transition metal oxide is uniformly distributed on the magnesium surface in addition, and make the microstructure of material enter nano-scale, can significantly improve catalytic performance.
The expression formula of nanometer of the present invention/amorphous state magnesium-transition metals oxides composite hydrogen storage material is:
Mg (or MgH
2)+x at.%M
yO
z, M is a transition metal, 0.05≤x≤5, y=2 or 3, z=3,4 or 5; Or
Mg (or MgH
2)+x at.%M
aO
b+ y at.%M
cO
d(M and M are transition metal, 0.05≤x+y≤5, a and c=2 or 3, b and d=3,4 or 5).
Transition metal oxide in nanometer of the present invention/amorphous state magnesium-transition metals oxides composite hydrogen storage material is Nb
2O
5, Fe
3O
4, V
2O
5And Cr
2O
3
Described transition metal oxide is chosen to be: Nb
2O
5Or Nb
2O
5With Cr
2O
3
The mol ratio of magnesium or magnesium hydride and transition metal oxide is 95-99.95%: 0.05-5% in nanometer of the present invention/amorphous state magnesium-transition metals oxides composite hydrogen storage material.
The granular size of nanometer of the present invention/amorphous state magnesium-transition metals oxides composite hydrogen storage material is between 10-500nm.
The preparation method of nanometer of the present invention/amorphous state magnesium-transition metals oxides composite hydrogen storage material comprises the steps:
(1) metal magnesium powder or magnesium hydride powder are measured than evenly mixing in ball grinder by mole with one or both transition metal oxide powder;
(2) under the protection of the nitrogen atmosphere (or argon atmospher) of 0.1-2MPa, be 150～500 rev/mins at rotating speed, ratio of grinding media to material is that ball milling got final product after 10～50 hours under 10～50: 1 the condition.
The equipment that the present invention uses is disclosed identical in Chinese patent CN1595688A with the applicant, employing be Germany product Fritsch P-6 planetary ball mill, important technological parameters is:
(1) ball grinder: material is a stainless steel, 250ml.
(2) ball: material is a stainless steel, and two kinds of specifications are arranged: φ 10mm (4g/) and φ 20mm (32g/).
(3) rotating speed: 100-600r/min.
(4) other: jar covered two passages, can feed the atmosphere of all gases with the control ball milling.
The present invention adopts the nanometer/amorphous state magnesium-transition metals oxides composite hydrogen storage material of high-energy ball milling method preparation can obviously improve the storage hydrogen dynamic performance of magnesium hydrogen storage material when keeping its high weight of hydrogen, also obviously reduces its hydrogen storage temperature simultaneously.Material of the present invention is suitable for the storage hydrogen carrier on the hydrogen fuel cell.
Description of drawings
Fig. 1 Mg+xmol.%Nb
2O
5X-ray diffractogram behind (x=0.2 and 1) ball milling 30h.
Fig. 2 Mg+1mol.%Nb
2O
5Sem photograph behind the ball milling 30h.
Fig. 3 Mg+1mol.%Nb
2O
5High-resolution transmission electron microscope behind the ball milling 30h and SEAD figure.
Fig. 4 Mg+1mol.%Nb
2O
5Behind the ball milling 30h in different temperatures, under the 2.5MPa hydrogen pressure storage hydrogen kinetic curve.
Fig. 5 Mg and Mg+2mol.%Cr
2O
3Behind the ball milling 30h at 523K, the storage hydrogen kinetic curve under the 2.5MPa hydrogen pressure.
Fig. 6 Mg+2mol.%Fe
3O
4Storage hydrogen kinetic curve behind the ball milling 30h under different temperatures, 2.5MPa hydrogen pressure.
Fig. 7 Mg+2mol.%V
2O
5Storage hydrogen kinetic curve behind the ball milling 30h under different temperatures, 2.5MPa hydrogen pressure.
Fig. 8 Mg and MgH
2+ 0.1mol.%Cr
2O
3+ 0.1mol.%Nb
2O
5Behind the ball milling 50h at 523K, the storage hydrogen kinetic curve under the 2.5MPa hydrogen pressure.
The specific embodiment
The present invention is described further below by example:
Embodiment 1:Mg+xmol.%Nb
2O
5The preparation of composite hydrogen storage material and storage hydrogen dynamic performance
With magnesium powder (purity, 99%, 100-200 order) and Nb
2O
5(purity, 99%, 100-200 order) presses Mg+xmol.%Nb
2O
5The stoichiometry of (x=0.05,0.1,0.2,0.5,1,2) is carried out proportioning.The preparation of employing high-energy ball milling method, ratio of grinding media to material is 20: 1, and sample jar is vacuumized, and fills hydrogen again, repeats 3 times to remove the air in the jar, charges into the high-purity hydrogen of 0.2MPa at last.The control rotating speed is 500r/min, behind the revolution 15min, leaves standstill 5min, and every ball milling 30min fills hydrogen one time, is 0.2MPa to guarantee hydrogen pressure, promptly gets required sample behind the ball milling 30h.Above all operations is all operated in vacuum glove box.Fig. 1 is Mg+xmol.%Nb
2O
5The X-ray diffractogram (XRD) of composite hydrogen storage material behind (x=0.2,1) ball milling 30h has only provided the collection of illustrative plates of x=0.1 and 1 here.Find out from this figure, along with Nb
2O
5The increase of content, the obvious broadening of all diffraction maximums shows that composite enters amorphous state.Rein in formula calculating, Mg+0.2mol.%Nb according to thanking
2O
5The grain size of middle Mg is 40nm.Fig. 2 is Mg+1mol.%Nb
2O
5The sem photograph of composite hydrogen storage material (SEM).As can be seen from this figure, the surface of much little particle attached to larger particles arranged, surface irregularity, and have a lot of fine cracks, this structure to be beneficial to the absorption and the diffusion of hydrogen.Fig. 3 is Mg+1mol.%Nb
2O
5The high-resolution transmission electron microscope (HRTEM) of composite hydrogen storage material and SEAD figure (SAED).As can be seen from this figure, have the existence of the diffraction pattern of the halo pattern of amorphous structure feature and polycrystalline attitude structure, illustrate that composite is nanometer/amorphous mixture.
Fig. 4 is Mg+1mol.%Nb
2O
5Composite hydrogen storage material is in different temperatures, under the 2.5MPa hydrogen pressure storage hydrogen kinetic curve.As can be seen from this figure, Mg+1mol.%Nb
2O
5Composite hydrogen storage material has just begun to store up hydrogen at 423K, and similar at the storage hydrogen curve shape of 423K during with 473K, maximum storage hydrogen percentage by weight is respectively 0.23% and 1.48%.When temperature surpassed 523K, storage hydrogen speed was obviously accelerated.When 523K, can finish 80% of maximum storage hydrogen quantity (5.3wt.%) in the 200s, Mean Speed is 2.2 * 10
-2Wt.%/s can finish 90% of maximum storage hydrogen quantity (5.9wt.%) in the 200s when 573K, Mean Speed is 3.0 * 10
-2Wt.%/s.
Embodiment 2:Mg+xmol.%Cr
2O
3The preparation of composite hydrogen storage material and storage hydrogen dynamic performance
The preparation method of this composite is identical with embodiment 1.With magnesium powder (purity, 99%, 100-200 order) and Cr
2O
3(purity, 99%, 100-200 order) presses x=0.05, and 0.1,0.2,0.5,1,2 stoichiometry is carried out proportioning.The preparation of employing high-energy ball milling method, ratio of grinding media to material is 30: 1, and sample jar is vacuumized, and fills hydrogen again, repeats 3 times to remove the air in the jar, charges into the high-purity hydrogen of 0.2MPa at last.The control rotating speed is 450r/min, behind the revolution 15min, leaves standstill 5min, and every ball milling 30min fills hydrogen one time, is 0.2MPa to guarantee hydrogen pressure, promptly gets required sample behind the ball milling 30h.The structure of composite is also similar to embodiment 1 with surface appearance feature, and promptly XRD, SEM, HRTEM and SAED scheme similar.Fig. 5 is pure Mg and Mg+2mol.%Cr
2O
3Composite hydrogen storage material is at 523K, the storage hydrogen kinetic curve under the hydrogen pressure of 2.5MPa.For the pure Mg hydrogen storage material through ball milling, storage hydrogen percentage by weight is 4.0% during 523K 400s, can finish more than 60% of maximum storage hydrogen quantity in the 100s, and Mean Speed is 2.3 * 10
-2Wt.%/s.And Mg+2mol.%Cr
2O
3Hydrogen storage content significantly increases when 523K, and storage hydrogen speed is also obviously accelerated, and hydrogen storage content reaches 5.2wt.% during 400s, finishes 90% of maximum storage hydrogen quantity in the 100s, and Mean Speed is 4.7 * 10
-2Wt.%/s.
Embodiment 3:Mg+xmol.%Fe
3O
4The preparation of composite hydrogen storage material and storage hydrogen dynamic performance
The preparation method of this composite is identical with embodiment 1.With magnesium powder (purity, 99%, 100-200 order) and Fe
3O
4(purity, 99%, 100-200 order) presses x=0.05, and 0.1,0.2,0.5,1,2 stoichiometry is carried out proportioning.The preparation of employing high-energy ball milling method, ratio of grinding media to material is 40: 1, and sample jar is vacuumized, and fills hydrogen again, repeats 3 times to remove the air in the jar, charges into the high-purity hydrogen of 0.2MPa at last.The control rotating speed is 400r/min, behind the revolution 15min, leaves standstill 5min, and every ball milling 30min fills hydrogen one time, is 0.2MPa to guarantee hydrogen pressure, promptly gets required sample behind the ball milling 30h.The structure of composite is also similar to embodiment 1 with surface appearance feature, and promptly XRD, SEM, HRTEM and SAED scheme similar.Fig. 6 is Mg+2mol.%Fe
3O
4The storage hydrogen kinetic curve of composite hydrogen storage material under different temperatures, 2.5MPa hydrogen pressure.As can be seen from this figure, this composite has begun to store up hydrogen at 423K, and it stores up hydrogen curve substantially linearly, and maximum storage hydrogen quantity is 0.6wt.%.During 473K, its storage hydrogen speed is accelerated to some extent, can finish more than 60% of maximum storage hydrogen quantity (2.8wt.%) in the 200s.Temperature surpasses 523K, and its hydrogen storage content significantly increases, and its storage hydrogen speed is obviously accelerated.The interior hydrogen storage content of 200s is 4.4wt.% during 523K, is 96% of maximum storage hydrogen quantity 4.6wt.%, and Mean Speed is 2.2 * 10
-2Wt.%/s; The interior hydrogen storage content of 200s is 4.6wt.% during 573K, is 96% of maximum storage hydrogen quantity 4.8wt.%, and Mean Speed is 2.3 * 10
-2Wt.%/s.
Embodiment 4:Mg+xmol.%V
2O
5The preparation of composite hydrogen storage material and storage hydrogen dynamic performance
The preparation method of this composite is identical with embodiment 1.With magnesium powder (purity, 99%, 100-200 order) and V
2O
5(purity, 99%, 100-200 order) presses x=0.05, and 0.1,0.2,0.5,1,2 stoichiometry is carried out proportioning.The preparation of employing high-energy ball milling method, ratio of grinding media to material is 50: 1, and sample jar is vacuumized, and fills hydrogen again, repeats 3 times to remove the air in the jar, charges into the high-purity hydrogen of 0.2MPa at last.The control rotating speed is 350r/min, behind the revolution 15min, leaves standstill 5min, and every ball milling 30min fills hydrogen one time, is 0.2MPa to guarantee hydrogen pressure, promptly gets required sample behind the ball milling 30h.The structure of composite is also similar to embodiment 1 with surface appearance feature, and promptly XRD, SEM, HRTEM and SAED scheme similar.Fig. 7 is Mg+2mol.%V
2O
5The storage hydrogen kinetic curve of composite hydrogen storage material under different temperatures, 2.5MPa hydrogen pressure.As can be seen from this figure, under the 2.5MPa hydrogen pressure, when temperature is 423K, this composite has begun to store up hydrogen, and its storage hydrogen curve is a straight line substantially, and hydrogen storage content is 0.9wt.% during 400s; Temperature is during greater than 473K, and its hydrogen storage content significantly increases, and storage hydrogen speed is obviously accelerated, and all can finish maximum storage hydrogen quantity (473K:3.4wt.% in the 100s; 523K:3.7wt.%; 573K:4.2wt.%) more than 90%, Mean Speed is respectively 3.0 * 10
-2Wt.%/s, 3.4 * 10
-2Wt.%/s and 4.0 * 10
-2Wt.%/s.
Embodiment 5:MgH
2+ xmol.%Cr
2O
3+ ymol.%Nb
2O
5The preparation of composite hydrogen storage material and storage hydrogen dynamic performance
At adding Cr
2O
3The storage hydrogen cycle performance of magnesium-base hydrogen storage material relatively good, and add Nb
2O
5The storage hydrogen dynamic performance of magnesium-base hydrogen storage material relatively good, attempt adopting at MgH
2In add two kinds of catalytic performances simultaneously and can improve its hydrogen storage property by complementary transition metal oxide.The preparation method of this composite is identical with embodiment 1.With magnesium hydride powder (MgH
2, purity 95%, 100-200 order), Cr
2O
3(purity, 99%, 100-200 order) presses x=0.05, and 0.1,0.2,0.5,1,2 and Nb
2O
5(purity, 99%, 100-200 order) presses x=0.05, and 0.1,0.2,0.5,1,2 stoichiometry is carried out proportioning.The preparation of employing high-energy ball milling method, ratio of grinding media to material is 20: 1, and sample jar is vacuumized, applying argon gas repeats 3 times to remove the air in the jar again, charges into the high-purity argon gas of 0.2MPa at last.The control rotating speed is 500r/min, behind the revolution 60min, leaves standstill 10min, and every ball milling 30min fills argon gas one time, to guarantee that gas pressure maintains 0.2MPa in the jar, promptly gets required sample behind the ball milling 50h.The structure of composite is also similar to embodiment 1 with surface appearance feature, and promptly XRD, SEM, HRTEM and SAED scheme similar.Fig. 8 is pure Mg and MgH
2+ 0.1mol.%Cr
2O
3+ 0.1mol.%Nb
2O
5Behind the ball milling 30h at 523K, the storage hydrogen kinetic curve under the 2.5MPa hydrogen pressure.For the pure Mg hydrogen storage material behind the ball milling, the interior hydrogen storage content of 250s is 3.6wt.% during 523K, can finish more than 25% of maximum storage hydrogen quantity in the 50s, and Mean Speed is 1.9 * 10
-2Wt.%/s; And MgH
2+ 0.1mol.%Cr
2O
3+ 0.1mol.%Nb
2O
5Hydrogen storage content significantly increases when 523K, and storage hydrogen speed is obviously accelerated, and the 250s hydrogen storage content reaches 5.9wt.%, and hydrogen storage content is finished more than 90% of maximum storage hydrogen quantity near 5.5wt.% in the 50s, and Mean Speed is 1.1 * 10
-1Wt.%/s.This composite hydrogen storage material is after the circulation suction of 400 weeks, putting hydrogen, and its hydrogen storage content does not have to change substantially, and its hydrogen desorption capacity has reduced 0.5wt.%.
Claims (7)
1. magnesium one transition metal oxide composite hydrogen storage material is characterized in that it is to form with magnesium metal or magnesium hydride and one or both transition metal oxides, and its expression formula is:
Mg or MgH
2+ x at.%M
yO
z, M is a transition metal, 0.05≤x≤5, y=2 or 3, z=3,4 or 5; Or
Mg or MgH
2+ x at.%M
aO
b+ y at.%M '
cO
d, M and M ' are transition metal, 0.05≤x+y≤5, a and c=2 or 3, b and d=3,4 or 5.
2. according to the described magnesium-transition metals oxides composite hydrogen storage material of claim 1, it is characterized in that described transition metal oxide is Nb
2O
5, Fe
3O
4, V
2O
5Or Cr
2O
3
3. according to claim 1 or 2 described magnesium-transition metals oxides composite hydrogen storage materials, it is characterized in that described transition metal oxide is Nb
2O
5Or Nb
2O
5With Cr
2O
3
4. according to claim 1,2 or 3 described magnesium-transition metals oxides composite hydrogen storage materials, it is characterized in that the mol ratio 95-99.95% of described magnesium or magnesium hydride and transition metal oxide: 0.05-5%.
5. according to each described magnesium-transition metals oxides composite hydrogen storage material of claim 1-4, the granular size that it is characterized in that it is between 10-500nm.
6. the preparation method of the described magnesium-transition metals oxides composite hydrogen storage material of claim 1 is characterized in that the concrete steps that it comprises:
(1) with metal magnesium powder or magnesium hydride powder and one or both transition metal oxide powder 95-99.95% in molar ratio: 0.05-5% evenly mixes in ball grinder;
(2) under the protection of the nitrogen atmosphere of 0.1-2MPa or argon atmospher, be 150～500 rev/mins at rotating speed, ratio of grinding media to material is a ball milling 10～50 hours under 10～50: 1 the condition.
7. the application of the described magnesium-transition metals oxides composite hydrogen storage material of claim 1 is characterized in that it is applicable to the accumulating or the hydrogen fuel cell of hydrogen.
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| CN110980635A (en) * | 2019-12-31 | 2020-04-10 | 世能氢电科技有限公司 | Preparation method of metal oxide composite magnesium hydride hydrogen storage material |
| CN111940719B (en) * | 2020-08-11 | 2022-07-19 | 江苏集萃安泰创明先进能源材料研究院有限公司 | Nano magnesium-based hydrogen storage material and preparation method thereof |
| CN113856670B (en) * | 2021-08-16 | 2023-11-24 | 广东省科学院资源利用与稀土开发研究所 | Catalytic MgH 2 Composite oxide for rapid hydrogen release and application thereof |
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