JP5650969B2 - Electrode material, spark plug electrode, and spark plug - Google Patents

Description

  The present invention relates to an electrode material used for an electrode of an ignition plug of an internal combustion engine included in an automobile or the like, an electrode made of the electrode material, and an ignition plug including the electrode. In particular, the present invention relates to an electrode material from which an electrode for a spark plug is obtained that is excellent in oxidation resistance at high temperature, is not easily consumed by a spark, and is difficult to form compound particles on the electrode surface.

  Conventionally, an ignition plug (spark plug) is used for ignition of an internal combustion engine such as an automobile gasoline engine. The spark plug typically includes a rod-shaped center electrode and a ground electrode disposed so as to face the end surface of the center electrode. A spark discharge is performed between the center electrode and the ground electrode, and this discharge ignites the fuel gas mixture flowing between the electrodes.

  As the electrode material, Patent Document 1 discloses a nickel alloy containing Al, Si, Cr, Mn, and Y.

Japanese Patent No. 4295501

  The characteristics required of an electrode of a spark plug are difficult to oxidize (oxidation resistance, particularly excellent oxidation resistance at high temperatures), hardly consumed by sparks (excellent resistance to spark consumption), and contains nickel on the electrode surface. It is desired that compound grains (described later) are difficult to be formed. The electrode material described in Patent Document 1 satisfies these requirements by containing a specific element.

  In recent years, it has been desired to improve the fuel efficiency of automobiles for environmental conservation measures. For example, fuel efficiency can be improved by increasing the combustion temperature in the internal combustion engine. However, by further increasing the combustion temperature, the spark plug electrode is used in a higher temperature environment than before. For example, the maximum temperature reached when using a conventional general gasoline engine of an automobile is about 900 ° C. to 1000 ° C., and when the combustion temperature is increased, a high temperature environment of about + 100 ° C. can be obtained.

  As described above, in recent years, the use environment of the spark plug has become much higher than before and can be said to be an environment that is more easily oxidized. Therefore, it is desired that the high-temperature oxidation resistance is superior among the above-mentioned various required characteristics.

  In order to enhance the oxidation suppression effect, it is effective to increase the content of Al or Si described in Patent Document 1. However, an increase in the additive element causes an increase in specific resistance, and as a result, it is easily consumed by a spark. Therefore, considering the spark wear resistance, there is a limit to improving the oxidation resistance against a further high temperature environment by increasing the content of additive elements such as Al and Si. Also, Al reacts with nitrogen in the atmosphere when using the spark plug to form nitride (AlN). Here, when an electrode made of a nickel alloy is used, an oxide layer is formed on the surface, and the oxidation on the surface is suppressed to some extent by the oxide layer on the surface. However, when the nitride is formed, the oxide layer is cracked due to thermal expansion or the oxide layer is peeled off, so that the oxidation tends to proceed easily. For this reason as well, even if Al is simply increased, there is a limit to improving the high-temperature oxidation resistance.

  Moreover, in the further high temperature environment as described above, the crystal grains constituting the electrode are likely to grow and become coarse. When the crystal grain boundary becomes shorter due to the coarsening, oxygen easily enters the electrode through the crystal grain boundary from the outside of the electrode, and the degree of penetration (depth) becomes deep, and it is easy to oxidize inside the electrode. Therefore, when used in a higher temperature environment, it is also desired to improve oxidation resistance by suppressing grain growth.

  On the other hand, when a spark plug is used, the electrode surface nickel reacts with elements in the atmosphere derived from gasoline, engine oil, etc. (alkali metal elements, alkaline earth metal elements, phosphorus, etc.), and the electrode surface In particular, a granular compound containing nickel (hereinafter referred to as a compound grain) is formed around the portion of the electrode where spark discharge is performed (mainly the surfaces facing each other in the center electrode and the ground electrode). This causes a phenomenon that the melting point of the adhering portion is partially lowered, the matrix phase is melted, and the compound particles are further enlarged. If the compound particles continue to be formed and grown, the ignition state of the engine may become unstable, or in the worst case, the compound particles may drop and damage the engine.

  Accordingly, an object of the present invention is to provide an electrode material that is excellent in high-temperature oxidation resistance and is not easily consumed by a spark and is difficult to form compound particles. Another object of the present invention is to provide a spark plug electrode made of the above electrode material, and a spark plug including the electrode.

The inventors of the present invention have obtained the following findings as a result of various investigations on more preferable compositions as the constituent material of the spark plug electrode particularly suitable for use in a high temperature environment.
(1) Ti has a high oxidation suppressing effect (particularly, an internal oxidation suppressing effect).
(2) By containing Ti in a specific range, an increase in specific resistance due to the Ti content can be suppressed, and the contents of Al and Si can be reduced.
(3) Ti can suppress nitriding of Al.
(4) Y is particularly effective in suppressing oxidation by effectively suppressing the growth of crystal grains at high temperatures and maintaining the fine crystal grains.
(5) Si tends to have a higher effect of suppressing oxidation than Al, and can suppress the formation of compound grains.
(6) Cr is effective in suppressing oxidation and suppressing the formation of compound grains.

  From the above findings, it is specified that Ti is contained in a specific range in addition to containing Al, Si, Cr, Y as the electrode material of the spark plug. In addition, it is defined that the contents of Al and Si are relatively reduced with the Ti content, that Si is contained more than Al, and the Y content is relatively increased.

  The electrode material of the present invention is an electrode material used for an electrode of a spark plug, and in mass%, Al is 0.005% to 0.2%, Si is 0.3% to 0.5%, Cr is 0.6% to 1.2%, It contains 0.05% to 0.5% Ti, 0.3% to 1.0% Y, and the balance consists of Ni and inevitable impurities.

  The electrode material of the present invention composed of a nickel alloy having the above specific composition includes (1) In addition to Al, Si, Cr, Y, Ti is contained in a specific range, so that the oxidation suppressing effect, particularly the internal oxidation can be achieved. The suppression effect is high, (2) By containing Ti, it is possible to suppress the nitridation of Al and suppress the occurrence of expansion, cracking, peeling, etc. of the oxide layer. (3) By containing Y in a specific range, It is excellent in oxidation resistance even when used in a high temperature environment because it can suppress the growth of crystal grains at high temperatures, and (4) it contains more Si than Al, so that it has a high oxidation suppression effect.

  In addition, the electrode material of the present invention (1) has a relatively low content of Al and Si, has a small specific resistance and is not easily consumed by a spark, and (2) contains Al, Si, Cr in a specific range. In particular, by containing more Cr than Al and Si, the formation and growth of the above-described compound grains can be effectively suppressed during use, and the specific resistance can be increased more than when containing a large amount of Al or Si. It is difficult to invite and has the effect of being excellent in spark wear resistance.

  Another form of the present invention includes a form further containing Mn. Specifically, Al is 0.005% to 0.2%, Si is 0.3% to 0.5%, Cr is 0.6% to 1.2%, Mn is 0.05% to 0.2%, and Ti is 0.05% or more by mass%. Examples include 0.5% or less, Y containing 0.3% or more and 1.0% or less, with the balance being Ni and inevitable impurities.

  Mn, like Cr, has the effect of suppressing the generation of the above compound grains, so Mn can be added together with Cr. In order to obtain the above effect, the content of Mn is preferably 0.05% by mass or more, and if it is 0.2% by mass or less, it is difficult to increase specific resistance.

  As one form of this invention, the form whose content of Al is 0.05 mass% or more and 0.2 mass% or less is mentioned.

  According to the said form, the oxidation suppression effect by containing Al can fully be acquired by containing 0.05 mass% or more of Al.

  As one form of the present invention, a form containing B more than 0 mass% and 0.05 mass% or less can be mentioned.

  According to the said form, by containing B, hot workability can be improved and productivity of an electrode material can be improved.

  As an embodiment of the present invention, an embodiment in which the electrode material has a specific resistance at room temperature of 20 μΩ · cm or less can be given.

  According to the said form, it is excellent also in spark wear resistance by a small specific resistance.

  As one form of the present invention, there is a form in which, when the electrode material is heated at 1000 ° C. for 72 hours, the average crystal grain size of the electrode material after heating is 300 μm or less.

  According to the above form, even when used in a very high temperature environment such as 1000 ° C. by being composed of a specific composition, the crystal grains are difficult to grow (not easily coarse), and the average crystal grain size is small. Can be maintained. Therefore, according to the said form, it is excellent in the oxidation resistance in high temperature.

  The spark plug electrode of the present invention or the spark plug electrode of the present invention composed of the above-mentioned electrode material of the present invention can be used even in a very high temperature environment of about 1000 ° C. or higher. Excellent in high temperature oxidation resistance. Furthermore, since the above-described spark wear resistance is excellent and the above-described compound particles are less likely to be produced, it is expected that the present spark plug electrode and the present spark plug can be used well over a long period of time.

  The electrode of the present invention composed of the electrode material of the present invention and the spark plug of the present invention including the electrode are excellent in high-temperature oxidation resistance.

FIG. 1 is an optical micrograph of an electrode material for explaining an oxidation state.

Hereinafter, the present invention will be described in more detail. In addition, unless otherwise indicated, content of an element shall be mass%.
[Electrode material]
(composition)
The electrode material of the present invention comprises Al, Si, Cr, Y and Ti as additive elements, with the balance being Ni and a nickel alloy with inevitable impurities. Ni is the main component (97 mass% or more (more preferably 98 mass% or more)). In addition to being excellent in plastic workability, it has low specific resistance (high conductivity) and is used for spark plug electrodes. If this happens, the consumption of sparks can be reduced.

《Al, Si》
Al and Si are elements that have a high effect of suppressing oxidation, and by containing both elements, an oxide of Al or Si is formed on the surface of the electrode material, reducing oxygen from entering the electrode material. In addition, oxidation, particularly internal oxidation can be suppressed. Further, by containing Al and Si together with Cr and Mn described later, there is an effect of suppressing the generation of the above-described compound grains. The more Al and Si, the easier the oxides are formed on the surface of the electrode material, which can suppress internal oxidation and suppress the generation / growth of compound grains, but if too much, the oxide formed on the surface of the electrode material The layer expands and cracks, cracks, or peels off. Oxidation progresses over time due to cracking or peeling of the oxide layer. In addition, the more Al and Si, the greater the specific resistance, which leads to a reduction in spark resistance. Therefore, the electrode material of the present invention contains both Al and Si, and the content thereof is relatively reduced. Instead, Ti is contained as an element having a high effect of suppressing internal oxidation. The specific contents are Al: 0.005% to 0.2%, Si: 0.3% to 0.5%. The Al content is more preferably 0.05% or more and 0.2% or less. Further, since Si tends to have a higher oxidation suppressing effect than Al, the electrode material of the present invention contains Si more than Al as described above.

《Y》
Y mainly forms an intermetallic compound with Ni of the parent phase and exists as an intermetallic compound, and a very small part thereof exists as a solid solution in Ni. Due to the so-called pinning effect of this intermetallic compound, the electrode material of the present invention can effectively suppress crystal grain growth even in a very high temperature environment such as 900 ° C. or higher, further 1000 ° C. or higher. Therefore, the electrode of the present invention made of the electrode material of the present invention is effective in internal oxidation because the crystal grains can be maintained in a fine state and oxygen intrusion can be reduced even when used in a very high temperature environment as described above. Can be suppressed. In order to have such excellent oxidation resistance, particularly high temperature oxidation resistance, it is preferable to contain 0.3% or more of Y. The more Y, the finer the crystal grains can be maintained and the higher the high temperature oxidation resistance tends to be It is in. In addition, by making the Y content 1.0% or less, the thermal deterioration of the electrode due to an increase in the specific resistance is suppressed, and the spark wear resistance is excellent. It is easy to process into an electrode and is excellent in electrode manufacturability. Furthermore, since Y is less likely to occlude hydrogen than other rare earth elements, the electrode material of the present invention hardly causes hydrogen embrittlement even when heat treatment is performed in an atmosphere containing hydrogen in the manufacturing process. A more preferable content of Y is 0.3% or more and 0.75% or less.

《Cr, Mn》
As described above, by containing Cr and Mn as appropriate together with Al and Si, the above-described compound particles are hardly generated. The reason for this is that Cr and Mn, together with Al and Si, react with elements in the atmosphere such as P contained in gasoline and engine oil to suppress the reaction between Ni and P in the parent phase, and Ni and P This is thought to be because it is possible to reduce the adhesion of compounds such as to the electrode material. In particular, Cr tends to have a higher effect of suppressing the generation of compound grains than Mn. Cr and Mn are also effective in suppressing internal oxidation, and Cr is less likely to increase the specific resistance than Al or Si. Therefore, the electrode material of the present invention contains Cr with less Al and Si as described above. The electrode material of the present invention appropriately contains Mn. As the content of Cr and Mn increases, the generation / growth and internal oxidation of the compound grains are more easily suppressed. However, when the content is too large, the specific resistance becomes too large. Therefore, the Cr content should be 0.6% or more and 1.2% or less. In particular, the Cr content is preferably 1.0% or less. When Mn is contained, the content of Mn is preferably 0.05% or more and 0.2% or less.

《Ti》
The electrode material of the present invention is characterized by containing Ti. Ti can effectively suppress internal oxidation as described above, and this effect becomes more prominent as the Ti content increases. However, if the Ti content is too large, the specific resistance increases. In addition, Ti suppresses the formation of Al nitride (AlN) as described above, and it is effective for the oxidation to proceed due to cracks in the oxide layer due to thermal expansion due to the formation of Al nitride. Can be suppressed. In order to sufficiently obtain the above effects, the Ti content is set to 0.05% to 0.5%. In particular, the Ti content is more preferably 0.1% or more and 0.3% or less.

《B》
By containing B in a range of 0.05% or less, preferably 0.001% or more and 0.02% or less, the hot workability is excellent, and the productivity of the electrode material of the present invention and the electrode of the present invention can be enhanced.

  The content of the additive element in the electrode material can be adjusted to the specific range by adjusting the amount of the element added as a raw material. In addition to the above additive elements, if high temperature strength is desired, it is allowed to contain a trace amount of C. However, if the amount of C is too large, the workability tends to deteriorate, so the C content is preferably 0.05% by mass or less.

(Oxidation resistance)
The electrode material of the present invention is excellent in high temperature oxidation resistance even when exposed to a high temperature environment such as 900 ° C. or higher, and further 1000 ° C. or higher, for example, to maintain a fine structure of crystal grains Can do. Specifically, when the electrode material is heated at 1000 ° C. for 72 hours, the average crystal grain size of the electrode material after heating can satisfy 300 μm or less. The condition of “1000 ° C x 72 hours” is very severe because it is the same temperature as or higher than the maximum temperature achieved when using a conventional general gasoline engine and the heating time is long. It mimics the conditions. Even when heating under such severe conditions, it is evaluated that the smaller the crystal grains constituting the electrode material, the more the oxygen can penetrate into the electrode material as described above, and the higher the resistance to high-temperature oxidation. can do. Therefore, in the present invention, “average crystal grain size after heating at 1000 ° C. × 72 hours” is adopted as an index for evaluating oxidation resistance. The average crystal grain size can be changed depending on the content of the additive element. For example, an electrode material satisfying 200 μm or less, further 150 μm or less, and particularly 100 μm or less can be obtained. As described above, the smaller the average grain size, the longer the crystal grain boundary, thereby making it easier to prevent oxygen from entering the electrode material, and there is no particular lower limit. “Average crystal grain size after heating at 1000 ° C. for 72 hours” tends to be smaller as the Y content increases.

(Resistivity)
The electrode material of the present invention has a small specific resistance, for example, a specific resistance at room temperature (typically about 20 ° C.) can satisfy 20 μΩ · cm or less. The specific resistance changes mainly depending on the content of the additive element, and the specific resistance tends to decrease as the content of the additional element decreases. The specific resistance is preferably as small as possible, and there is no particular lower limit.

(shape)
The electrode material of the present invention typically includes a wire formed by wire drawing. The cross-sectional shape can be various shapes such as a rectangular shape and a circular shape.

[Production method]
The electrode material of the present invention is typically obtained by a process of melting → casting → hot rolling → cold drawing and heat treatment. Further, in order for the intermetallic compound containing Y to be sufficiently present in the electrode material, for example, the atmosphere during melting or casting is controlled so that the oxygen concentration becomes low. Since Y is easy to form an oxide, it is easy to form an intermetallic compound by suppressing the formation of the oxide of Y by casting or the like in a low oxygen atmosphere.

  When performing the final heat treatment (softening treatment) after cold drawing, 700 ° C to 1000 ° C in a non-oxidizing atmosphere (e.g., an oxygen atmosphere such as a hydrogen atmosphere, a nitrogen atmosphere, or an oxygen-free atmosphere). In particular, it is preferable to carry out at about 800 ° C to 950 ° C. By performing such a softening process, it is easy to process the electrode material into a predetermined electrode shape, or the processing distortion due to the process before the softening process can be removed, and the specific resistance of the electrode material can be reduced.

[Spark plug electrode]
The electrode material of the present invention can be suitably used for any constituent material of the center electrode and the ground electrode provided in the spark plug. In many cases, the ground electrode is disposed closer to the center of the combustion chamber in an internal combustion engine such as an automobile engine than the center electrode. Since the electrode material of the present invention is excellent in characteristics at a high temperature as described above, it can be suitably used particularly as a constituent material of the ground electrode. The electrode of the present invention can be produced by cutting the electrode material into an appropriate length or further forming it into a predetermined shape.

[Ignition plug]
The electrode of the present invention can be suitably used as a constituent member of a spark plug used for ignition in an internal combustion engine such as an automobile engine. The spark plug of the present invention typically includes an insulator, a metal shell that holds the insulator, a center electrode that is held in the insulator and partially protrudes from the tip of the insulator, and the above One having one end welded to the front end surface of the metal shell and the other end facing the end surface of the center electrode and a terminal metal fitting provided at the rear end of the insulator. Can be mentioned. The electrode of the present invention can be used in place of a known spark plug electrode.

Hereinafter, more specific embodiments of the present invention will be described.
A plurality of nickel alloy wires (electrode materials) were prepared as materials for spark plug electrodes used for ignition of general automobile gasoline engines, and their characteristics were evaluated.

  Each wire was produced as follows. Using an ordinary vacuum melting furnace, a nickel alloy melt having the composition shown in Table 1 (unit: mass%) was produced. Commercially available pure Ni (99.0 mass% or more Ni) and grains of each additive element were used as the raw material for the molten metal. In addition, the molten metal was refined to reduce and remove impurities and inclusions. The above refining condition was adjusted so that any sample did not substantially contain C. Then, the atmosphere was controlled so as to reduce the oxygen concentration, the above melting was performed, the molten metal temperature was appropriately adjusted, and vacuum casting was performed to obtain an ingot (2 tons).

  The obtained ingot was reheated and forged to obtain a billet of about 150 mm square. This billet was hot-rolled to obtain a rolled wire having a wire diameter of 5.5 mmφ. The rolled wire rod was subjected to a combination of cold wire drawing and heat treatment to obtain each cold wire rod having a wire diameter of 2.5 mmφ and a wire diameter of 4.2 mmφ. The cold-drawn wire with a wire diameter of 2.5 mmφ was rolled and deformed into a 1.5 mm × 2.8 mm rectangular wire, thereby obtaining a rectangular wire. Final flat heat treatment (softening treatment, temperature: 800 ° C to 1000 ° C, non-oxidizing atmosphere (nitrogen atmosphere or hydrogen atmosphere), using continuous softening furnace) is applied to the obtained rectangular wire and cold drawn wire with a wire diameter of 4.2 mmφ. Thus, a soft material (electrode material) was obtained. Each soft material obtained was cut into an appropriate length and then molded into a predetermined shape as appropriate, and a spark plug ground electrode (1.5 mm x 2.8 mm rectangular wire) used in general ordinary passenger cars. Use), a spark plug center electrode (using a wire diameter of 4.2 mmφ) was prepared and used as a sample.

  When the composition of each sample obtained (here, the soft material) was examined using an ICP emission spectroscopic analyzer, it was the same as the composition shown in Table 1, with the balance being Ni and inevitable impurities. In addition, the Ni content in each sample was 90% by mass or more (sample Nos. 1 to 8 were 98% by mass or more Ni). The composition can be analyzed by the atomic absorption spectrophotometry method as well as the above ICP emission spectroscopic analysis method. In Table 1, “-(hyphen)” is less than the detection limit and indicates that it is not substantially contained. Furthermore, when each sample containing Y was examined using elemental analysis by SEM and EDX, or EPMA, it was confirmed that an intermetallic compound of Y and Ni was present.

《Specific resistance》
The specific resistance of each prepared sample (soft material) was measured. The results are shown in Table 2. The specific resistance (room temperature) was measured by a DC four-terminal method using an electrical resistance measuring apparatus (distance between grades GL = 100 mm).

<Oxidation resistance>
Each manufactured sample (soft material) was evaluated for high-temperature oxidation resistance. The results are shown in Table 2. High-temperature oxidation resistance is achieved by inserting the ground electrode made of the above-mentioned 1.5 mm x 2.8 mm flat soft material and the center electrode made of soft material with a wire diameter of 4.2 mmφ into an atmospheric furnace heated to 1000 ° C. Then, after heating for 1 hour, the sample was taken out of the furnace, air-cooled for 30 minutes, and then heated again for 1 hour. A high-temperature oxidation test was repeated until the heating time reached a total of 72 hours.

  After the high temperature oxidation test, the cross section of the ground electrode was observed with an optical microscope (magnification: 50 to 200 times), and the thickness of the oxidized region (oxide layer) of the electrode using this microscopic observation image (photograph) Was measured. Here, when an oxide layer is formed on an electrode made of a Ni alloy, a two-layer structure is formed as shown in FIG. Specifically, the surface oxide layer is formed on the outermost surface of the electrode and in the vicinity thereof, the content of the additive element is high, the content of Ni is low, and the surface oxide layer is formed inside the surface oxide layer. With many internal oxide layers. The electrode shown in FIG. 1 is a conventional electrode, which is an explanatory sample in which the high temperature oxidation test was performed under the condition of 900 ° C. × 72 hours. In this test, the thicknesses of the inner oxide layer and the surface oxide layer were measured. Specifically, the thickness of the internal oxide layer is the average thickness from the boundary between the parent phase region composed of Ni alloy and the internal oxide layer to the boundary between the internal oxide layer and the surface oxide layer, For the surface oxide layer, the average thickness from the boundary between the two oxide layers to the outermost surface of the electrode was measured. The average thickness can be easily obtained by performing image processing or the like on the observed image. It can be said that the lower the degree of oxygen intrusion into the electrode, the thinner the internal oxide layer and the less internal oxidation occurs. In addition, about the center electrode, since it was the tendency similar to a ground electrode, the result is not described.

  And, when the total thickness of the surface oxide layer and the internal oxide layer is 200 μm or more, the high-temperature oxidation resistance is X, and the total thickness is 200 μm. Those with less than were evaluated as ◯, and those with the above expansion, cracks, and peeling were described as such. A case where the total thickness was less than 190 μm and there was almost no expansion or cracking was evaluated as “Excellent” as being particularly good.

<Average crystal grain size>
For each sample after the above high-temperature oxidation test, the cross section of the ground electrode was observed with an optical microscope (magnification: 50 to 200 times), and the cross line method (line method) was used for this microscope observation image (photograph). The average crystal grain size was calculated. The results are shown in Table 2. In addition, a sample having an average crystal grain size of 300 μm or less was evaluated as ◯, and a sample having a mean crystal grain size of more than 300 μm was evaluated as ×.

《Sparkproof wear resistance》
The spark wear resistance correlates with the specific resistance of the electrode material. Accordingly, for each of the above prepared samples, those having a specific resistance at room temperature of more than 20 μΩ · cm are marked as poor in spark wear resistance, and those having a specific resistance of 20 μΩ · cm or less are marked as good in terms of spark wear resistance. The results are shown in Table 2.

<< Formation of compound grains >>
About each produced said sample, the generation | occurrence | production state of the compound grain was investigated as follows. The results are shown in Table 2. The engine oil is applied to the 1.5 mm × 2.8 mm flat soft material described above, and the soft material is set in an annular heating furnace capable of controlling the atmosphere. Here, the heating furnace is heated to 1100 ° C so that the combustion temperature is about 100 ° C higher than the combustion temperature (about 900 ° C to 1000 ° C) in a general automobile gasoline engine, and a test gasoline engine (displacement volume) The sample is held for 60 hours in an atmosphere simulating the inside of the engine while exhaust gas discharged from 2000 cc, 6 cylinders) flows into the furnace. The surface state of each sample after this heating test was observed with a magnifying glass.

  As a result of the above observations, the case where large compound particles are present and the sample is greatly swollen or the compound particles are generated over the entire surface is x. When the compound particles are generated and the surface of the sample is large, the conventional material As a rule, Δ was evaluated as ◯, when the generation of compound particles was slight, and ◯ when the generation of compound particles was hardly observed. The results are shown in Table 2.

  As shown in Table 2, sample Nos. 1 to 8 containing Al, Si, Cr, Y, and Ti in a specific range are excellent in oxidation resistance even at a high temperature of 1000 ° C. or higher. I understand. Specifically, in all of sample Nos. 1 to 8, the difference between the thickness of the surface oxide layer and the thickness of the internal oxide layer is small, and the internal oxide layer is not extremely thick. One reason for this is thought to be that internal oxidation could be suppressed by containing a small amount of Al or Si and containing appropriate amounts of Cr and Ti. Further, in any of the sample Nos. 1 to 8, the oxide layer is not substantially expanded, cracked or peeled off. One reason for this is thought to be that a small amount of Al or Si was contained. Further, all of the sample Nos. 1 to 8 have fine crystal grains even when exposed to the high temperature as described above. One reason for this is considered to be that an appropriate amount of Y was contained. From this, it is considered that all of sample Nos. 1 to 8 could have excellent high-temperature oxidation resistance.

  In addition, it can be seen that all of Sample Nos. 1 to 8 have a small specific resistance of 20 μΩ · cm or less. One reason for this is thought to be because Al and Si are not excessively contained. Moreover, since the specific resistance is small, when using sample No. 1-8 for an electrode for spark plugs, it is thought that it is excellent in spark wear resistance. Further, it can be seen that all of the sample Nos. 1 to 8 hardly generate compound grains. One reason for this is that by containing Al, Si, and Cr, and optionally Mn, it was possible to suppress the formation of low melting point compounds between the elements in the atmosphere and the parent phase Ni. It is believed that there is.

  In contrast, Sample Nos. 100 and 120 to 127 that do not contain the specific element in a specific range are particularly thick in the internal oxide layer, expanded, cracked, or peeled off in the oxide layer. It can be seen that grains are generated and crystal grains are coarse. That is, when an electrode for a spark plug is formed from a wire that does not contain the specific element in a specific range, and this electrode is used in a higher temperature environment than before, sufficient resistance to high-temperature oxidation and resistance to sparks is sufficient. It can be said that compound grains are also likely to be generated.

  As described above, an electrode material containing Al, Si, Cr, Y, and Ti, and optionally Mn in a specific range is excellent in high-temperature oxidation resistance, has a low specific resistance, and does not easily generate compound grains. . Therefore, the electrode for a spark plug made from this electrode material is expected to be used well even in an environment where the temperature is higher than before (for example, an ultra-high temperature environment of the conventional temperature + 100 ° C.). . Further, the above-mentioned electrode is difficult to form an oxide layer excessively, the oxide layer hardly expands, cracks, and peels off, has a small specific resistance and is less consumed by sparks, and the above-mentioned compound particles are formed. It is expected to have a long life because it is difficult to grow.

  The above-described embodiment can be appropriately changed without departing from the gist of the present invention, and is not limited to the above-described configuration. For example, the composition, shape, size, etc. of the electrode material can be changed as appropriate. Further, the composition can be made different between the ground electrode and the center electrode.

  The electrode material of the present invention can be suitably used as a constituent material for spark plug electrodes of various internal combustion engines such as automobile engines. The electrode of the present invention can be suitably used for the components of the spark plug. The spark plug of the present invention can be suitably used as an ignition member for the internal combustion engine.

Claims (4)

An electrode material used for an electrode of a spark plug,
% By mass
Al is 0.005% or more and 0.2% or less,
Si is 0.3% to 0.5%,
Cr is 0.6% or more and 1.2% or less,
Ti 0.05% or more and 0.5% or less,
Containing Y 0.3% or more and 1.0% or less, with the balance being Ni and inevitable impurities,
An electrode material having an average crystal grain size of 100 μm or less when the electrode material is heated at 1000 ° C. for 72 hours.   2. The electrode material according to claim 1, further comprising 0.05% by mass to 0.2% by mass of Mn. An ignition plug electrode comprising the electrode material according to claim 1 or 2 . A spark plug comprising the spark plug electrode according to claim 3 .