Metal treatment – Stock – Magnesium base
Reexamination Certificate
1999-03-17
2004-01-27
Ip, Sikyin (Department: 1742)
Metal treatment
Stock
Magnesium base
C420S543000, C420S544000, C420S545000, C420S536000, C429S218200
Reexamination Certificate
active
06682609
ABSTRACT:
BACKGROUND OF THE INVENTION
This invention relates to a hydrogen-absorbing alloy, a method of modifying the surface of the hydrogen-absorbing alloy, negative electrode for battery and an alkaline secondary battery.
Hydrogen-absorbing alloy is known as being capable of stably absorbing and storing hydrogen several ten thousands times (calculated as a gas under normal temperature and pressure) as much as of its own volume. Therefore, hydrogen-absorbing alloy is noticed as a promising material for safely and easily storing, keeping and transporting hydrogen as an energy source. Hydrogen-absorbing alloy is also studied for utilization in a chemical heat pump or compressor by making most of a difference in property between hydrogen-absorbing alloys, some of them being developed for actual use. Recently, the application of hydrogen-absorbing alloys to a metal hydride secondary battery (for example, nickel-hydrogen secondary battery) as an energy source by making use of hydrogen stored in a hydrogen-absorbing alloy, as well as an electrode material by making use of its high catalytic activity in the absorption and desorption reaction of the hydrogen-absorbing alloys has been extensively developed.
As evident from these facts, the hydrogen-absorbing alloy has many possibilities for various applications in view of its physical and chemical characteristics, so that the hydrogen-absorbing alloy is now considered as being one of important raw materials in future industrial.
The metal capable of absorbing hydrogen and constituting the hydrogen-absorbing alloy may be in the form of single substance which reacts exothermically with hydrogen, i.e., a metal element capable of forming a stable compound together with hydrogen (for example, platinum group elements, lanthanum group elements and alkaline earth elements); or in the form of an alloy comprising such a metal, as mentioned above, alloyed with another kind of metals. One of the advantages of the alloy resides in that the bonding strength between a metal and hydrogen can be suitably weakened so that not only the absorption reaction but also the desorption reaction can be performed comparatively easily. Second advantage of the alloy resides in that the absorption and desorption characteristics of the alloy with respect to the magnitude of hydrogen gas pressure required for the reaction (equilibrium pressure; plateau pressure), the extent of equilibrium region (plateau region), the change (flatness) of equilibrium pressure during the process of absorbing hydrogen and the like can be improved. Third advantage of the alloy resides in the improvement in chemical and physical stability.
The composition of the conventional hydrogen-absorbing alloy may be classified into the following types; i.e., (1) an AB
5
type (for example, LaNi
5
, CaNi
5
); (2) an AB
2
type (for example, MgZn
2
, ZrNi
2
); (3) an AB type (for example, TiNi, TiFe); (4) an A
2
B type (for example, Mg
2
Ni, Ca
2
Fe); and other types (for example, cluster), wherein A represents a metal element which is capable of exothermically reacting with hydrogen, and B, another kind of metal. Among them, LaNi
5
of (1), a laves phase alloy belonging to (2) and some kinds of alloy belonging to (3) are capable of reacting with hydrogen at the normal temperature, and chemically stable so that they are extensively studied as a candidate for an electrode material of a secondary battery.
Whereas, the hydrogen-absorbing alloy belonging to (4) A
2
B type is accompanied with the following problems. Namely, the alloy strongly attract hydrogen so that hydrogen once absorbed therein can be hardly released. The absorption and desorption reaction thereof occurs only when the temperature thereof is raised up to a relatively high degree (about 200 to 300° C.), and the rate of the reaction, if occurred, is slow. The chemical stability, in particular the stability in an aqueous solution, of the alloy is comparatively low. The alloy is generally very viscous and hard so that the working such as pulverization of it is very difficult. In view of these facts, the hydrogen-absorbing alloy of A
2
B type is rarely utilized except for the storage and transport of hydrogen in spite of its excellent capacity of absorbing hydrogen which is comparable to other types of hydrogen-absorbing alloy on the basis of volume and, if calculated on the basis of weight, two to several times as high as that of other types of hydrogen-absorbing alloy. Therefore, of these problems inherent to the hydrogen-absorbing alloy of A
2
B type as explained above are solved, it would be possible to expand the application of the alloy not only to the same fields as those of other types of hydrogen-absorbing alloy but also to a new field of utilization.
By the way, there have been reported a number of academic papers on the hydrogen-absorbing alloy of this (5) type. However, up to date, the report of practical use or testing for practical use is almost none.
Meanwhile, there is disclosed in Jpn. Pat. KOKAI Publication No. 6-76817 a magnesium-based hydrogen-absorbing alloy represented by a composition formula of Mg
2−x
Ni
1−y
A
y
B
x
(wherein x is 0.1 to 1.5; y is 0.1 to 0.5; A represents an element selected from Sn, Sb and Bi; B represents an element selected from Li, Na, K and Al) such for example as Mg
1.5
Al
0.5
Ni
0.7
Sn
0.3
; or Mg
1.8
Al
0.2
Ni
0.8
Sn
0.2
. There is also disclosed in this publication that the hydrogen-absorbing alloy can be utilized as a negative electrode material of an alkali secondary battery. However, since this hydrogen-absorbing alloy disclosed in the publication is fundamentally of A
2
B type, the hydrogen-absorbing and desorbing property thereof in the normal temperature region is poor. Therefore, in order to make it possible to absorb and desorb hydrogen under normal temperature and pressure, the hydrogen-absorbing alloy is covered on the surface thereof with a nickel metal compound or a phosphorous compound as disclosed in the publication.
As explained above, the A
2
B type hydrogen-absorbing alloy has a feature distinct from other types of hydrogen-absorbing alloy in that it is light in weight, large in capacity and low in raw material cost since its composition is mainly consisted of alkaline earth metals and iron group elements. However, the A
2
B type hydrogen-absorbing alloy is accompanied with various problems as explained above.
BRIEF SUMMARY OF THE INVENTION
Accordingly, an object of the present invention is to provide a hydrogen-absorbing alloy which is chemically stable, in particular in an aqueous solution, and can be easily pulverized by way of mechanical means.
Another object of this invention is to provide a hydrogen-absorbing alloy which is improved of its hydrogen-absorbing property, in particular the hydrogen-absorbing at room temperature.
Another object of this invention is to provide a method of modifying the surface activity of the hydrogen-absorbing alloy so that hydrogen can be easily and sufficiently absorbed by the hydrogen-absorbing alloy.
A further object of this invention is to provide a negative electrode for a secondary battery, which is excellent in stability during the electrode reaction, and to provide an alkali secondary battery having an improved charge/discharge cycle property.
A still further object of this invention is to develop a means to evaluate the deteriorating rate of a hydrogen-absorbing alloy containing magnesium, and, on the basis of this means, to provide a negative electrode suited for practical use, which is excellent in the reversibility and stability in the electrode reaction and an alkali secondary battery provided with such a negative electrode.
Namely, according to the present invention, there is provided a hydrogen-absorbing alloy containing an alloy represented by the following general formula (I):
Mg
2
M1
y
(I)
wherein M1 is at least one element selected (excluding Mg, elements which are capable of causing an exothermic reaction with hydrogen, Al and B) from elements which are incapable of causing an exothermic reaction with hyd
Kanda Motoya
Kohno Tatsuoki
Tsuruta Shinji
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