Porous aluminum sintered compact and method of producing porous aluminum sintered compact

Abstract

A high-quality porous aluminum sintered compact, which can be produced efficiently at a low cost; has an excellent dimensional accuracy with a low shrinkage ratio during sintering; and has sufficient strength, and a method of producing the porous aluminum sintered compact are provided. The porous aluminum sintered compact is the porous aluminum sintered compact (10) that includes aluminum substrates (11) sintered to each other. The junction (15), in which the aluminum substrates (11) are bonded to each other, includes the Ti—Al compound (16) and the Mg oxide (17). It is preferable that the pillar-shaped protrusions projecting toward the outside are formed on outer surfaces of the aluminum substrates (11), and the pillar-shaped protrusions include the junction (15).

Claims

1. A porous aluminum sintered compact comprising a plurality of aluminum substrates sintered to each other, wherein a junction, in which the plurality of aluminum substrates are bonded to each other, includes a Ti—Al compound and a Mg oxide, the plurality of aluminum substrates are made of aluminum fibers or both of aluminum fibers and an aluminum powder, a ratio of the aluminum powder in the plurality of aluminum substrates is 15 mass % or less, a plurality of pillar-shaped protrusions projecting toward an outside are formed on outer surfaces of the plurality of aluminum substrates, the pillar-shaped protrusions include the junction, a porosity of the porous aluminum sintered compact is in a range of 56.5% or more and less than 90%, and the aluminum fibers are subjected to a shape-added processing which is a torsion processing.

2. A method of producing the porous aluminum sintered compact according to claim 1, the method comprising the steps of: forming an aluminum raw material for sintering by adhering a titanium powder, which is made of any one of or both of a titanium metal powder and a titanium hydride powder, and a magnesium powder on outer surfaces of the plurality of aluminum substrates; spreading the aluminum raw material for sintering on a holder; and sintering the aluminum raw material held on the holder by heating, wherein the plurality of aluminum substrates are bonded through a junction including a Ti—Al compound and the a Mg oxide.

3. The method of producing the porous aluminum sintered compact according to claim 2, wherein the junction is formed on a plurality of pillar-shaped protrusions projecting toward an outside from outer surfaces of the plurality of aluminum substrates.

4. The method of producing the porous aluminum sintered compact according to claim 2, wherein a content amount of the titanium powder in the aluminum raw material for sintering is set in a range of 0.01 mass % or more and 20 mass % or less, and a content amount of the magnesium powder in the aluminum raw material for sintering is set in a range of 0.01 mass % or more and 5 mass % or less in the step of forming an aluminum raw material for sintering.

5. The method of producing the porous aluminum sintered compact according to claim 2, wherein the step of forming an aluminum raw material for sintering comprises the steps of: mixing the plurality of aluminum substrates; and the titanium powder and the magnesium powder in a presence of a binder; and drying a mixture obtained in the step of mixing.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is an enlarged schematic view of the porous aluminum sintered compact of an embodiment related to the present invention.

(2) FIG. 2 is a diagram showing an SEM observation and composition analysis results of the junction between the aluminum substrate of the porous aluminum sintered compact shown in FIG. 1.

(3) FIG. 3 is a flow diagram showing an example of the method of producing the porous aluminum sintered compact shown in FIG. 1.

(4) FIG. 4 is an explanatory diagram of the aluminum raw material for sintering in which the titanium powder and the magnesium powder are adhered on the surfaces of the aluminum substrates.

(5) FIG. 5 is a schematic illustration of the continuous sintering apparatus for producing the porous aluminum sintered compact in a sheet shape.

(6) FIG. 6 is an explanatory diagram showing the state where the pillar-shaped protrusions are formed on the outer surfaces of the aluminum substrates in the step of sintering.

(7) FIG. 7 is an explanatory diagram showing the production process for producing the porous aluminum sintered compact in a bulk-shape.

DESCRIPTION OF EMBODIMENTS

(8) The porous aluminum sintered compact 10, which is an embodiment of the present invention, is explained below in reference to the attached drawings.

(9) The porous aluminum sintered compact 10, which is an embodiment of the present invention, is shown in FIG. 1. As shown in FIG. 1, the porous aluminum sintered compact 10 of the present embodiment is what the aluminum substrates 11 are integrally combined by sintering; and the porosity of the porous aluminum sintered compact 10 is set to the range of 10% or more and 90% or less.

(10) In the present embodiment, the aluminum fibers 11a and the aluminum powder 11b are used as the aluminum substrates 11 as shown in FIG. 1.

(11) The porous aluminum sintered compact 10 has the structure, in which the pillar-shaped protrusions 12 projecting toward the outside are formed on the outer surfaces of the aluminum substrates 11 (the aluminum fibers 11a and the aluminum powder 11b); and the aluminum substrates 11 (the aluminum fibers 11a and the aluminum powder 11b) are bonded to each other through the pillar-shaped protrusions 12. As shown in FIG. 1, the junctions 15 between the aluminum substrates 11, 11 include: a part in which the pillar-shaped protrusions 12, 12 are bonded to each other; a part in which the pillar-shaped protrusion 12 and the side surface of the aluminum substrate 11 are bonded to each other; and a part in which the side surfaces of the aluminum substrates 11, 11 are bonded to each other.

(12) The junction 15 of the aluminum substrates 11, 11 bonded to each other through the pillar-shaped protrusion 12, includes the Ti—Al compound 16 and the Mg oxide 17 as shown FIG. 2. The Ti—Al compound 16 is a compound of Ti and Al in the present embodiment as shown in the analysis results of FIG. 2. More specifically, it is Al.sub.3Ti intermetallic compound. In addition, the Mg oxide 17 locates at the surface layer of the junction 15 and the aluminum substrate 11. In other words, the aluminum substrates 11, 11 are bonded to each other in the part where the Ti—Al compound 16 and the Mg oxide 17 exist in the present embodiment.

(13) Next, the aluminum raw material for sintering 20, which is the raw material of the porous aluminum sintered compact 10 of the present embodiment, is explained. The aluminum raw material for sintering 20 includes: the aluminum substrate 11; and the titanium powder grains 22 and the magnesium powder grains 23, both of which are adhered on the outer surface of the aluminum substrate 11, as shown in FIG. 4. As the titanium powder grains 22, any one or both of the metal titanium powder grains and the titanium hydride powder grains can be used. As the magnesium oxide grain 23, the metal magnesium powder grains are used.

(14) In the aluminum raw material for sintering 20, the content amount of the titanium powder grains 22 is set to the range of 0.01 mass % or more and 20 mass % or less. In the present embodiment, it is set to 5 mass %.

(15) The grain size of the titanium powder grains 22 is set to the range of 1 μm or more and 50 μm or less. Preferably, it is set to 5 μm or more and 30 μm or less. The titanium hydride powder grains can be set to a value finer than that of the metal titanium powder grains. Thus, in the case where the grain size of the titanium powder grains 22 adhered on the outer surface of the aluminum substrate 11 is set to a fine value, it is preferable that the titanium hydride powder grains are used.

(16) Moreover, it is preferable that the distance between the titanium powder grains 22, 22 adhered on the outer surface of the aluminum substrate 11 is set to the range of 5 μm or more and 100 μm or less.

(17) In addition, in the aluminum raw material for sintering 20, the content amount of the magnesium powder grains 23 is set to the range of 0.01 mass % or more and 5 mass % or less. In the present embodiment, it is set to 1.0 mass %.

(18) The grain size of the magnesium powder grains 23 is set to the range of 20 μm or more and 200 μm or less. Preferably, it is set to the range of 20 μm or more and 80 μm or less.

(19) As the aluminum substrate 11, the aluminum fibers 11a and the aluminum powder 11b are used as described above. As the aluminum powder 11b, an atomized powder can be used.

(20) The fiber diameter of the aluminum fiber 11a is set to the range of 40 μm or more and 1000 μm or less. Preferably, it is set to the range of 50 μm or more and 500 μm or less. The fiber length of the aluminum fiber 11a is set to the range of 0.2 mm or more and 100 mm or less. Preferably, it is set to the range of 1 mm or more and 50 mm or less.

(21) The aluminum fiber 11a is made of pure aluminum or an aluminum alloy, for example; and the ratio L/R of the length L to the fiber diameter R may be set to the range of 4 or more and 2500 or less. The aluminum fiber 11a can be obtained by the step of forming the aluminum raw material for sintering, in which any one or both of the Mg powder and the Mg alloy powder are adhered on its outer surface and the aluminum raw material for sintering is formed, for example. In the step of sintering, the aluminum raw material for sintering can be sintered at the temperature range of 590° C. to 665° C. under an inert gas atmosphere.

(22) In the case where the fiber diameter R of the aluminum fiber 11a is less than 20 μm, sufficient sintered strength might not be obtained due to too small junction area of the aluminum fibers. On the other hand, in the case where the fiber diameter R of the aluminum fiber 11a is more than 1000 μm, sufficient sintered strength might not be obtained due to lack of contact points of the aluminum fibers.

(23) Because of the reasons described above, in the porous aluminum sintered compact 10 of the present embodiment, the fiber diameter R of the aluminum fiber 11a is set to the range of 20 μm or more and 1000 μm or less. In the case where more improved sintered strength is needed, it is preferable that the fiber diameter of the aluminum fiber ha is set to 50 μm or more; and the fiber diameter of the aluminum fiber 11a is set to 500 μm or less.

(24) In the case where the ratio L/R of the length L of the aluminum fiber 11a to the fiber diameter R is less than 4, it becomes harder to keep the bulk density DP in a stacking arrangement at 50% of the true density DT of the aluminum fiber or less in the method of producing the porous aluminum sintered compact. Thus, obtaining the porous aluminum sintered compact 10 having high porosity could be difficult. On the other hand, in the case where the ratio L/R of the length L of the aluminum fiber 11a to the fiber diameter R is more than 2500, it becomes impossible to disperse the aluminum fibers 11a evenly. Thus, obtaining the porous aluminum sintered compact 10 having uniform porosity could be difficult.

(25) Because of the reasons described above, in the porous aluminum sintered compact 10 of the present embodiment, the ratio L/R of the length L of the aluminum fiber 11a to the fiber diameter R is set to the range of 4 or more and 2500 or less. In the case where more improved porosity is needed, it is preferable that the ratio L/R of the length L to the fiber diameter R is set to 10 or more. In addition, in order to obtain the porous aluminum sintered compact 10 having more uniform porosity, it is preferable that the ratio L/R of the length L to the fiber diameter R is set to 500 or more.

(26) The grain size of the aluminum powder 11b is set to the range of 20 mm or more and 300 μm or less. Preferably, it is set to the range of 20 μm or more and 100 μm or less.

(27) As the aluminum fiber 11a, any one of the pure aluminum and the general aluminum alloys can be suitably used.

(28) In the case where an aluminum alloy is used as the aluminum fiber 11a, the A3003 alloy (Al—0.6 mass % Si—0.7 mass % Fe—0.1 mass % Cu—1.5 mass % Mn—0.1 mass % Zn alloy), the A5052 alloy

(29) (Al—0.25 mass % Si—0.40 mass % Fe—0.10 mass % Cu—0.10 mass % Mn—2.5 mass % Mg—0.2 mass % Cr—0.1 mass % Zn alloy) as defined in JIS, and the like can be named for example.

(30) As the aluminum powder 11b, the pure aluminum powder and/or an aluminum alloy powder may be used. For example, the powder made of JIS A3003 alloy or the like can be used.

(31) The shape of the aluminum fiber 11a can be selected arbitrary, such as a liner shape, a curved shape, and the like. However, if ones subjected to a predetermined shape-added processing, such as torsion processing, bending processing, and like, on at least a part of the aluminum fibers 11a were used, the shapes of void between the aluminum fibers 11a would be formed three-dimensionally and isotopically. As a result, isotropy of various characteristics of the porous aluminum sintered compact, such as the heat-transfer property and the like, is improved. Thus, it is preferable.

(32) In addition, the porosity can be controlled by adjusting the mixing rate of the aluminum fibers 11a and the aluminum powder 11b. More specifically, the porosity of the porous aluminum sintered compact can be improved by increasing the ratio of the aluminum fiber 11a. Because of this, it is preferable that the aluminum fibers 11a are used as the aluminum substrates 11. In the case where the aluminum powder 11b is mixed in, it is preferable that the ratio of the aluminum powder 11b in the aluminum substrates is set to 15 mass % or less.

(33) Next, the method of producing the porous aluminum sintered compact 10 of the present embodiment is explained in reference to the flow diagram in FIG. 3 and the like.

(34) First, the aluminum raw material for sintering 20, which is the raw material of the porous aluminum sintered compact 10 of the present embodiment, is produced as shown in FIG. 3.

(35) The above-described aluminum substrates 11, the titanium powder, and the magnesium powder are mixed at room temperature (the mixing step S01). At this time, the binder solution is sprayed on. As the binder, what is burned and decomposed during heating at 500° C. in the air is preferable. More specifically, using an acrylic resin or a cellulose-based polymer material is preferable. In addition, various solvents such as the water-based, alcohol-based, and organic-based solvents can be used as the solvent of the binder.

(36) In the mixing step S01, the aluminum substrates 11, the titanium powder, and the magnesium powder are mixed by various mixing machine, such as an automatic mortar, a pan type rolling granulator, a shaker mixer, a pot mill, a high-speed mixer, a V-shaped mixer, and the like, while they are fluidized.

(37) Next, the mixture obtained in the mixing step S01 is dried (the drying step S02). By the mixing step S01 and the drying step S02, the titanium powder grains 22 and the magnesium powder grain 23 are dispersedly adhered on the surfaces of the aluminum substrates 11 as shown in FIG. 4; and the aluminum raw material for sintering 20 in the present embodiment is produced. It is preferable that the titanium powder grains 22 are dispersed in such a way that the distance between the titanium powder grains 22, 22 adhered on the outer surfaces of the aluminum substrates 11 is set to the range of 5 μm or more and 100 μm or less.

(38) Next, the porous aluminum sintered compact 10 is produced by using the aluminum raw material for sintering 20 obtained as described above.

(39) In the present embodiment, the porous aluminum sintered compact 10 in the long sheet shape of 300 mm of width; 1-5 mm of thickness; and 20 m of length, is produced, for example, by using the continuous sintering apparatus 30 shown in FIG. 5.

(40) This continuous sintering apparatus 30 has: the powder spreading device 31 spreading the aluminum raw material for sintering 20 evenly; the carbon sheet 32 holding the aluminum raw material for sintering 20 supplied from the powder spreading device 31; the transport roller 33 driving the carbon sheet 32; the degreasing furnace 34 removing the binder by heating the aluminum raw material for sintering 20 transported with the carbon sheet 32; and the sintering furnace 35 sintering the binder-free aluminum raw material for sintering 20 by heating.

(41) First, the aluminum raw material for sintering 20 is spread toward the upper surface of the carbon sheet 32 from the powder spreading device 31 (the raw material spreading step S03).

(42) The aluminum raw material for sintering 20 spread on the carbon sheet 32 spreads in the width direction of the carbon sheet 32 during moving toward the traveling direction F to be uniformed and formed into a sheet shape. At this time, load is not placed upon. Thus, voids are formed between the aluminum substrates 11 in the aluminum raw material for sintering 20. In the present embodiment, a shape-added processing, such as torsion processing, bending processing, and like, is performed on the aluminum fibers 11 in the aluminum substrates 11 used for the aluminum raw material for sintering 20. Thus, three dimensional and isotropic voids are maintained between the stacked aluminum raw materials for sintering 20.

(43) Next, the aluminum raw material for sintering 20, which is shaped into a sheet-shape on the carbon sheet 32, is inserted in the degreasing furnace 34 with the carbon sheet 32; and the binder is removed by being heated at a predetermined temperature (the binder removing step S04).

(44) In the binder removing step S04, the aluminum raw material for sintering 20 is maintained at 350° C. to 500° C. for 0.5 to 5 minutes in the air atmosphere; and the binder in the aluminum raw material for sintering 20 is removed. In the present embodiment, the binder is used only for adhering the titanium powder grains 22 and the magnesium powder grains 23 on the outer surfaces of the aluminum substrates 11 as described above. Thus, the content amount of the binder is extremely low compared to the viscous compositions; and the binder can be removed sufficiently in a short time.

(45) Next, the aluminum raw material for sintering 20 free of the binder is inserted in the sintering furnace 35 with the carbon sheet 32 and sintered by being heated at a predetermined temperature (the sintering step S05).

(46) The sintering step S05 is performed by maintaining the aluminum raw material for sintering 20 at 590° C. to 665° C. for 0.5 to 60 minutes in an inert gas atmosphere. Depending on the content amount of Mg in the aluminum raw material for sintering 20, the optimum sintering temperature differs. However, in order to permit high-strength and uniform sintering, the sintering temperature is set to 590° C., which is the liquidus-line temperature of Al—10 mass % Mg, or more. In addition, it is set to 665° C. or less in order to prevent rapid progression of sintering shrinkage due to combining of melts in the formed liquid phases. Preferably, the retention time is set to 1 to 20 minutes.

(47) In the sintering step S05, the optimum temperature differs depending on the content amount of Mg in the aluminum raw material for sintering 20 as described above. However, sintering is performed by heating at the temperature of 590° C. to 665° C., which is close to the melting point of the aluminum substrate 11, in any case. Thus, the aluminum substrates 11 in the aluminum raw material for sintering 20 are melted. Since the oxide films are formed on the surfaces of the aluminum substrates 11, the melted aluminum is held by the oxide film; and the shapes of the aluminum substrates 11 are maintained.

(48) In addition, by being heated at 590° C. to 665° C., in the part where the titanium powder grains 22 are adhered among the outer surfaces of the aluminum substrates 11, the oxide files are destroyed by the reaction with titanium; and the melted aluminum inside spouts out. The spouted out melted aluminum forms a high-melting point compound by reacting with titanium to be solidified. Because of this, the pillar-shaped protrusions 12 projecting toward the outside are formed on the outer surfaces of the aluminum substrates 11 as shown in FIG. 6. On the tip of the pillar-shaped protrusion 12, the Ti—Al compound 16 exists. Growth of the pillar-shaped protrusion 12 is suppressed by the Ti—Al compound 16.

(49) In the case where titanium hydride is used as the titanium powder grains 22, titanium hydride is decomposed near the temperature of 300° C. to 400° C.; and the produced titanium reacts with the oxide films on the surfaces of the aluminum substrates 11.

(50) In addition, in the present embodiment, a part of the oxide films formed on the surfaces of the aluminum substrates is reduced by the magnesium powder grains 23 adhered on the outer surfaces of the aluminum substrates 11; and a large number of the pillar-shaped protrusions 12 are formed. More specifically, it is understood that it is because of thinning of the oxide films by: the magnesium powder grains 23 being sublimed to be dispersed in the oxide films; and reducing the oxide films

(51) At this time, the adjacent the aluminum substrates 11, 11 are bonded to each other by being combined integrally in a molten state or being sintered in a solid state through the pillar-shaped protrusions 12 of each. Accordingly, the porous aluminum sintered compact 10, in which the aluminum substrates 11, 11 are bonded to each other through the pillar-shaped protrusions 12 as shown in FIG. 1, is produced. In addition, the junction 15, in which the aluminum substrates 11, 11 are bonded to each other through the pillar-shaped protrusion 12, includes the Ti—Al compound 16 (Al.sub.3Ti intermetallic compound in the present embodiment) and the Mg oxide 17.

(52) In the porous aluminum sintered compact 10 of the present embodiment configured as described above, the junction 15 of the aluminum substrates 11, 11 includes the Ti—Al compound 16. Thus, the oxide films formed on the surfaces of the aluminum substrates 11 are removed by the Ti—Al compound 16; and the aluminum substrates 11, 11 are bonded properly to each other. Therefore, the high-quality porous aluminum sintered compact 10 having sufficient strength can be obtained.

(53) In addition, since the growth of the pillar-shaped protrusions 12 is suppressed by the Ti—Al compound 16, spouting out of the melted aluminum into the voids between the aluminum substrates 11, 11 can be suppressed; and the porous aluminum sintered compact 10 having high porosity can be obtained.

(54) Especially, Al.sub.3Ti exists as the Ti—Al compound 16 in the junction 15 of the aluminum substrates 11, 11 in the present embodiment. Thus, the oxide films formed on the surfaces of the aluminum substrates 11 are removed reliably; and the aluminum substrates 11, 11 are bonded properly to each other. Therefore, strength of the porous aluminum sintered compact 10 can be ensured.

(55) In addition, in the present embodiment, the junction 15 includes the Mg oxide 17. Thus, a part of the oxide films formed on the surfaces of the aluminum substrates 11 is reduced; and a large number of the junctions 15 of the aluminum substrates 11, 11 each other can be formed. Accordingly, strength of the porous aluminum sintered compact 10 can be improved significantly.

(56) In addition, the porous aluminum sintered compact 10 has the structure in which the aluminum substrates 11, 11 are bonded to each other through the pillar-shaped protrusions 12 formed on the outer surfaces of the aluminum substrates 11. Thus, the porous aluminum sintered compact 10 having high porosity can be obtained without performing the step of foaming or the like separately. Therefore, the porous aluminum sintered compact 10 of the present embodiment can be produced efficiently at low cost.

(57) Especially, the continuous sintering apparatus 30 is used in the present embodiment. Thus, the sheet-shaped porous aluminum sintered compact 10 can be produced continuously; and the production efficiency can be improved significantly.

(58) Moreover, the content amount of the binder is extremely low compared to the viscous compositions in the present embodiment. Thus, the binder removing step S04 can be performed in a short time. In addition, the shrinkage rate during sintering becomes about 1%, for example; and the porous aluminum sintered compact 10 having excellent dimensional accuracy can be obtained.

(59) In addition, the aluminum fibers 11a and the aluminum powder 11b are used as the aluminum substrates 11 in the present embodiment. Thus, the porosity of the porous aluminum sintered compact 10 can be controlled by adjusting the mixing rates.

(60) In addition, the porosity is set to the range of 30% or more and 90% or less in the porous aluminum sintered compact 10 of the present embodiment. Thus, it is possible to provide the porous aluminum sintered compact 10 having an optimal porosity depending on the application.

(61) In addition, the content amount of the titanium powder grains 22 in the aluminum raw material for sintering 20 is set to 0.01 mass % or more and 20 mass % or less in the present embodiment. Thus, the pillar-shaped protrusions 12 can be formed with an appropriate distance therebetween on the outer surfaces of the aluminum substrates 11. Accordingly, the porous aluminum sintered compact 10 having sufficient strength and high porosity can be obtained.

(62) In addition, the distance between the titanium powder grains 22, 22 each other adhered on the outer surfaces of the aluminum substrates 11 is set to the range of 5 μm or more and 100 μm or less in the present embodiment. Thus, the distance between the pillar-shaped protrusions 12 is set appropriately. Accordingly, the porous aluminum sintered compact 10 having sufficient strength and high porosity can be obtained.

(63) In addition, the content amount of the magnesium powder grains 23 in the aluminum raw material for sintering 20 is set to 0.01 mass % or more and 5 mass % or less in the present embodiment. Thus, by reducing the oxide films on the surfaces of the aluminum substrates 11 at an appropriate extent, a large number of the pillar-shaped protrusions 12 can be formed with an appropriate distance therebetween. Accordingly, the porous aluminum sintered compact 10 having sufficient strength and high porosity can be obtained.

(64) In addition, the fiber diameter of the aluminum fiber 11a, which is the aluminum substrate 11, is set to the range of 40 μm or more and 500 μm or less; and the grain size of the aluminum powder 11b is set to the range of 20 μm or more and 300 μm or less in the present embodiment. In addition, the grain size of the titanium powder grains 22 is set to the range of 1 μm or more and 50 μm or less; and the grain size of the magnesium powder grains 23 is set to the range of 20 μm or more and 150 μm or less. Therefore, the titanium powder grains 22 and the magnesium powder grains 23 are dispersedly adhered on the outer surfaces of the aluminum substrates 11 (the aluminum fibers 11a and the aluminum powder 11b) reliably.

(65) In addition, the aluminum fibers 11a and the aluminum powder 11b are used as the aluminum substrates 11; and the ratio of the aluminum powder 11b relative to the aluminum substrates 11 is set to 15 mass % or less in the present embodiment. Thus, the porous aluminum sintered compact 10 with high porosity can be obtained.

(66) Another method of producing the porous aluminum sintered compact is described below.

(67) For example, the aluminum fibers 11a; and any one or both of the Mg powder and Mg alloy powder 23, are mixed at room temperature. During mixing, a binder solution is sprayed on. As the binder, what is burned and decomposed during heating at 500° C. in the air is preferable. More specifically, using an acrylic resin or a cellulose-based polymer material is preferable. In addition, various solvents such as the water-based, alcohol-based, and organic-based solvents can be used as the solvent of the binder.

(68) During mixing, the aluminum fibers 11a and the Mg powder 23 are mixed by various mixing machine, such as an automatic mortar, a pan type rolling granulator, a shaker mixer, a pot mill, a high-speed mixer, a V-shaped mixer, and the like, while they are fluidized.

(69) Next, by drying the mixture obtained by mixing, the Mg powder and the Mg alloy powder 23 are dispersedly adhered on the outer surfaces of the aluminum fibers 11a; and the aluminum raw material for sintering 20 in the present embodiment is produced.

(70) Next, during producing the porous aluminum sintered compact 10 by using the aluminum raw material for sintering 20 obtained as described above, the porous aluminum sintered compact 10 in the long sheet shape of: 300 mm of width; 1-5 mm of thickness; and 20 m of length, is produced, for example, by using a continuous sintering apparatus or the like for example.

(71) For example, the aluminum raw material for sintering 20 is spread toward the upper surface of the carbon sheet from a raw material spreading apparatus; the aluminum raw material for sintering 20 is stacked; and the aluminum raw material for sintering 20 stacked on the carbon sheet is shaped into a sheet-shape. At this time, voids are formed between the aluminum fibers 11a in the aluminum raw material for sintering 20.

(72) At this time, for example, the aluminum fibers 11a are stacked in such a way that the bulk density after filling becomes 50% of the true density of the aluminum fibers to maintain three-dimensional and isotropic voids between the aluminum fibers 11a in stacking.

(73) Next, the aluminum raw material for sintering 20, which is shaped into the sheet-shape on the carbon sheet, is inserted in the degreasing furnace; and the binder is removed by being heated at a predetermined temperature. At this time, the aluminum raw material for sintering is maintained at 350° C. to 500° C. for 0.5 to 5 minutes in the air atmosphere; and the binder in the aluminum raw material for sintering is removed. In the present embodiment, the binder is used only for adhering the Mg powder and the Mg alloy powder 23 on the outer surfaces of the aluminum fibers 11a. Thus, the content amount of the binder is extremely low compared to the viscous compositions; and the binder can be removed sufficiently in a short time.

(74) Next, the aluminum raw material for sintering 20 free of the binder is inserted in the sintering furnace with the carbon sheet and sintered by being heated at a predetermined temperature.

(75) The sintering is performed by maintaining the aluminum raw material for sintering at 590° C. to 665° C. for 0.5 to 60 minutes in an inert gas atmosphere, for example. Depending on the content amount of Mg in the aluminum raw material for sintering 20, the optimum sintering temperature differs. However, in order to permit high-strength and uniform sintering, the sintering temperature is set to 590° C., which is the liquidus-line temperature of Al—10 mass % Mg, or more. In addition, it is set to 665° C. or less in order to prevent rapid progression of sintering shrinkage due to combining of melts in the formed liquid phases. Preferably, the retention time is set to 1 to 20 minutes.

(76) In the sintering, a part of the aluminum fibers 11a in the aluminum raw material for sintering 20 is melted. However, since the oxide films are formed on the surfaces of the aluminum fibers 11a, the melted aluminum is held by the oxide film; and the shapes of the aluminum fibers 11a are maintained.

(77) In the part where the Mg powder grains, the Mg alloy powder grains 23 are adhered among the outer surfaces of the aluminum fibers 11a, Mg functions as a reducing agent for the oxide films of Al.sub.2O.sub.3; the oxide films are destroyed; and formation of sintered bonding is stimulated. In addition, by Mg, which is adhered on the surfaces of the aluminum fibers, reacting locally with the aluminum fibers, the melting point lowering effect is obtained locally in the vicinity of the adhering parts. As a result, the liquid phase is formed at an even lower temperature than the melting point of the pure aluminum fibers or the aluminum alloy fibers; and sintering is stimulated to improve strength compared to the case free of Mg addition.

(78) Since Mg diffuses into the aluminum fibers gradually with progression of sintering, Mg exists in solid solution or in the form of Mg oxide in the finally obtained porous aluminum sintered compact.

(79) Embodiments of the present invention are explained above. However, the present invention is not particularly limited by the description of the embodiments; and the present invention can be modified as need in the range that does not depart from the technical concept of the present invention as defined in the scope of the present invention.

(80) For example, it is explained that the porous aluminum sintered compact is continuously produced by using the continuous sintering apparatus shown in FIG. 5.

(81) However, the present invention is not limited by the description, and the porous aluminum sintered compact may be produced by using other producing apparatus

(82) In addition, the sheet-shaped porous aluminum sintered compacts are explained in the present embodiment. However, the present invention is not particularly limited by the description, and it may be the bulk-shaped porous aluminum sintered compact produced by the production process shown in FIG. 7, for example.

(83) As shown in FIG. 7, the aluminum raw material for sintering 20 is spread to bulk fill (the raw material spreading step) on the carbon-made container 132 from the powder spreader 131 spreading the aluminum raw material for sintering 20. Then, the container 132 is inserted in the degreasing furnace 134; and the binder is removed by heating under air atmosphere (the binder removing step). Then, the container is inserted in the sintering furnace 135; and heated to and retained at 590° C. to 665° C. under an Ar atmosphere to obtain the bulk-shaped porous aluminum sintered compact 110. The bulk-shaped porous aluminum sintered compact 110 can be taken out from the carbon-made container 132 relatively easily, since a carbon-made container having excellent mold releasing characteristics is used as the carbon-made container 132; and the content is shrunk in the shrinkage rate about 1% during sintering.

EXAMPLES

(84) Results of confirmatory experiments performed to confirm the technical effect of the present invention are explained below.

(85) By the methods shown in the above-described embodiments and using the raw materials shown in Table 1, the aluminum raw materials for sintering were prepared. The aluminum fibers, the fiber diameter of which was 40 μm or more and 500 μm or less; and the aluminum powder, the grain size of which was 20 μm or more and 300 μm or less, were used as the aluminum substrates

(86) By the production methods shown in the above-described embodiments and using these aluminum raw materials for sintering, the porous aluminum sintered compacts having the dimension of: 30 mm of width; 200 mm of length; and 5 mm of thickness, were produced. More specifically, the sintering step was performed in the condition of: in the highly-pure argon atmosphere; at a sintering temperature appropriately selected based on each of aluminum raw materials between 590° C. to 655° C.; and the retention time of 15 minutes for each.

(87) With respect to the obtained porous aluminum sintered compacts, the apparent porosity and the tensile strength were evaluated. The evaluation results are shown in Table 1. The evaluation methods are shown below.

(88) [Apparent Porosity]

(89) The mass m (g), the volume V (cm.sup.3), and the true density d (g/cm.sup.3) were measured in the obtained porous aluminum sintered compacts; and the apparent porosity was calculated by suing the formula shown below.
Apparent Porosity (%)=(1−(m/(V×d)))×100

(90) The true density (g/cm.sup.3) was measured by the water method with the precision balance.

(91) [Tensile Strength]

(92) The tensile strength of the obtained porous aluminum sintered compacts was measured by the pulling method.

(93) [Metal Structure of the Junction]

(94) Identification and distribution state of the Ti—Al compound and the Mg oxide in the junction were obtained by the energy dispersive X-ray spectroscopy (EDX method) or the electron micro analyzer (EPMA method).

(95) TABLE-US-00001 TABLE 1 Titanium powder Magnesium powder Aluminum substrate Grain Content Grain Content Sintering Apparent Tensile Fiber Powder size amount size amount temperature porosity strength Material (%) (%) Material (μm) (mass %) (μm) (mass %) (° C.) (%) (N/mm.sup.2) Examples 1 A1070 94.0 — Titanium 1.0 5.0 30.0 1.0 630 74.2 3.5 of the hydride present 2 A1070 94.0 — Titanium 5.0 5.0 30.0 1.0 645 72.0 3.1 invention hydride 3 A1070 94.0 — Metal 30.0 5.0 30.0 1.0 645 73.2 2.8 titanium 4 A1070 94.0 — Metal 50.0 5.0 30.0 1.0 630 75.0 2.5 titanium 5 A1070 98.99 — Titanium 5.0 0.01 30.0 1.0 635 74.0 1.5 hydride 6 A1070 79.0 — Titanium 5.0 20.0 30.0 1.0 640 70.6 2.8 hydride 7 A1070 94.0 — Titanium 5.0 5.0 20.0 1.0 640 74.3 3.4 hydride 8 A1070 94.0 — Titanium 5.0 5.0 75.0 1.0 640 74.0 3.0 hydride 9 A1070 94.99 — Titanium 5.0 5.0 30.0 0.01 655 73.0 2.5 hydride 10 A1070 90.0 — Titanium 5.0 5.0 30.0 5.0 645 71.5 3.6 hydride 11 A1070 89.0 5.0 Titanium 5.0 5.0 30.0 1.0 650 69.2 2.9 hydride 12 A1070 84.0 10.0 Titanium 5.0 5.0 30.0 1.0 655 68.5 3.2 hydride 13 A1050 96.0 — Titanium 5.0 0.5 30.0 3.5 655 56.5 7.0 hydride 14 A1050 96.0 — Titanium 5.0 2.0 50.0 2.0 645 60.1 4.9 hydride 15 A1050 97.3 — Titanium 5.0 2.0 30.0 0.7 650 65.5 4.1 hydride 16 A1050 93.5 — Titanium 5.0 5.0 30.0 1.5 640 69.3 3.7 hydride 17 A1050 94.0 — Titanium 5.0 5.0 30.0 1.0 630 74.6 2.1 hydride 18 A1050 85.5 — Titanium 5.0 10.0 20.0 4.5 600 83.7 1.3 hydride 19 A3003 98.5 — Titanium 10.0 1.0 30.0 0.5 620 60.3 4.4 hydride 20 A3003 94.0 — Titanium 5.0 5.0 30.0 1.0 605 70.4 2.4 hydride 21 A3003 84.0 — Titanium 5.0 12.0 20.0 4.0 595 82.6 1.5 hydride 22 A5052 98.7 — Titanium 10.0 1.0 30.0 0.3 630 59.0 6.4 hydride 23 A5052 93.5 — Titanium 5.0 5.0 30.0 1.5 600 68.8 4.2 hydride 24 A5052 84.5 — Titanium 5.0 12.0 20.0 3.5 590 80.5 1.7 hydride Comparative A1070 80.0 — Titanium 5.0 20.0 — — 660 70.2 0.5 Example 1 hydride Comparative A1070 100.0 — — — — — — 662 75.0 0.1 Example 2

(96) In Examples 1 to 24 of the present invention, in which the aluminum raw materials including the magnesium powders were used, it was confirmed that strength was improved sufficiently even though they had apparent porosities equivalent to Comparative Examples 1 and 2, in which the aluminum raw materials free of the magnesium powder were used as shown in Table 1.

(97) Based on the observation, it was confirmed that the high-quality porous aluminum sintered compact having high porosity and sufficient strength could be provided according to the present invention.

REFERENCE SIGNS LIST

(98) 10, 110: Porous aluminum sintered compact 11: Aluminum substrate 11a: Aluminum fiber 11b: Aluminum powder 12: Pillar-shaped protrusion 15: Junction 16: Ti—Al compound 17: Mg oxide 20: Aluminum raw material for sintering 22: Titanium powder grain (Titanium powder) 23: Magnesium powder grain (Magnesium powder)