Patent Application
20070264491
Additional objects and advantages of the present invention will be more readily apparent from the following detailed description of preferred embodiments when taken together with the accompanying drawings. In the drawings:
As shown in
The coating structure 1 can be used for the metal member 10 made of a various metal-based material. An example material for the metal member 10 is a Fe-based material. When the coating structure 1 is formed on the Fe-based member 10, the coating structure 1 can provide a waterproof property (e.g., water-shedding property) effectively. In the first embodiment, an austenitic stainless steel (SUS304) consisting mainly of Fe is used. A surface roughness Rz(10) of the metal member 10 is about 2 μm, and the surface of the metal member 10 is uneven.
Between the metal member 10 and the composite film 11, two layers for increasing an adhesiveness of the composite film 11 are formed. One layer is a Ni strike film 13 formed directly on the metal member 10, as an adhesion layer. The other layer is a NiP film 14 formed directly on the Ni strike film 13, as a ground layer.
A preferred thickness of each of the Ni strike film 13 and the NiP film 14 is about in a range of 0.5 to 1.5 μm. When the thickness is under 0.5 μm, the adhesiveness of the composite film 11 may be not improved effectively. When the thickness is over 1.5 μm, a production cost of the coating structure 1 becomes high. In the first embodiment, the thickness of the Ni strike film 13 is 1 μm, and the thickness of the NiP film 14 is 1 μm, as an example.
The Ni strike film 13 may be formed by an electroplating, and the NiP film 14 may be formed by an electroless plating, for example. In each case, the Ni strike film 13 and the NiP film 14 are formed with high accuracies.
On the NiP film 14, the composite film 11 is formed. In the composite film 11, the PTFE particles are dispersed in the NiP as a base material. A preferred particle size of the PTFE particles is about in a range of 0.2 to 1 μm. When the particle size is under 0.2 μm, the composite film 11 may not provide the water-shedding property effectively. When the particle size is over 1 μm, it may be difficult to disperse the PTFE particles uniformly. A preferred content rate of the PTFE particles in the composite film is about in a range of 7 to 9 wt %. When the content rate of the PTFE particles in the composite film is under 7 wt %, the water-shedding property of the composite film 11 may be reduced. When the content rate of PTFE particles in the composite film is over 9 wt %, a heat-resistance of the composite film 11 may be reduced.
The composite film 11 may be formed by an electroless plating. In this case, the composite film 11 may be formed with a high accuracy. The composite film 11 may be formed by another method, such as an electroplating.
A preferred thickness of the composite film 11 is about in a range of 5 to 20 μm. When the thickness of the composite film 11 is under 5 μm, the composite film 11 may be difficult to be formed with the high accuracy on the metal member 10 having the large surface roughness. When the thickness of the composite film 11 is over 20 μm, it may be difficult to control the thickness. Therefore, more preferred thickness of the composite film 11 is about in a range of 5 to 15 μm.
In the first embodiment, a particle size of the PTFE particles is about in a range of 0.2 to 1 μm, the content rate of the PTFE particles in the composite film is about in a range of 7 to 9 wt % (i.e., 22 to 26 vol %), and a thickness of the composite film 11 is 10 μm, as an example.
A preferred surface roughness Rz of a surface, on which the composite film 11 is formed, i.e., a surface roughness Rz of a layer under the composite film 11, is not more than about 5 μm. When the surface roughness Rz is over 5 μm, a sick may be occurred in the composite film 11, and the composite film 11 may be not formed with the high accuracy. In the first embodiment, the surface roughness Rz of the surface, on which the composite film 11 is formed, i.e., a surface roughness Rz(14) of the NiP film 14 is 0.03 μm, as an example.
On the composite film 11, the fluorine-based film 12 is formed. The fluorine-based film 12 includes a fluoroalkylsilane. Therefore, the fluorine-based film 12 has a sufficient water-shedding property. A preferred thickness of the fluorine-based film 12 is about in a range of 0.01 to 0.5 μm. When the thickness of the fluorine-based film 12 is under 0.01 μm, a detachment and a deterioration of the fluorine-based film 12 may be occurred easily, and a durability of the fluorine-based film 12 may be reduced. When the thickness of the fluorine-based film 12 is over 0.5 μm, it may be difficult to control the thickness of the fluorine-based film 12. In the first embodiment, the thickness of the fluorine-based film 12 is 0.1 μm, as an example.
A preferred surface roughness Rz(11) of the composite film 11 is not more than about 0.1 μm. When the surface roughness Rz(11) is over 0.1 μm, the fluorine-based film 12 formed on the composite film 11 may have a sink, and may be not formed with a high accuracy. In the first embodiment, the surface roughness Rz(11) is 0.03 μm, as an example.
Next, a method for forming the coating structure 1 will be described. Before forming the various layers, a sample piece as the metal member 10 is preliminary cleaned with following four cleaning processes.
At first, the sample piece 10 is soaked in an alkaline cleaner (PAKUNA200TA made by Yuken Industry Co., Ltd.) at 60° C. for 10 min, and is rinsed by water. Then, the sample piece 10 is soaked in a hydrochloric acid aqueous solution at room temperature for 10 min, and is rinsed by water. Next, the sample piece 10 is soaked in an electrolytic cleaner (ASAHI CLEANER C-4000 made by C. Uyemura & Co., Ltd.), is electrolytic cleaned at 60° C. and at 2 A/dm2 of current density for 10 min, and is rinsed by water. Additionally, the sample piece 10 is soaked in the hydrochloric acid aqueous solution at room temperature for 5 min, and is rinsed by water.
Next, as shown in
Next, the fluorine-based film 12 is formed on the composite film 11 of the sample piece 10, by using a coating apparatus 4. As shown in
The sample piece 10 is set to the holding part 41 of the filming apparatus 4. The holding part 41 is moved downward, and the sample piece 10 is soaked in a fluorine-containing solution 120 (e.g., fluoroalkylsilane: 1 to 20 wt %, alkylsilane: 1 to 10 wt %, a surfactant, and a deformer) such that a surface on which the fluorine-based film 12 should be formed is perpendicular to the liquid surface of the fluorine-containing solution 120. Then, the holding part 41 is moved upward, and the sample piece 10 is pulled-out from the fluorine-containing solution 120 at the predetermined rate, e.g., 30 mm/min. After that, the sample piece 10 is dried at 280° C. for 10 min for forming the fluorine-based film 12. In this way, the coating structure 1 in
In the coating structure 1, the fluorine-based film 12 is not formed directly on the metal member 10, but formed on the composite film 11 as the surface-smoothing layer which is formed on the metal member 10. Therefore, the coating structure 1 can be used for the metal member 10 having the large surface roughness, and has the sufficient water-shedding property which is not reduced by heating.
In other words, in the coating structure 1, the composite film 11 including NiP as the base material is formed on the metal member 10. The composite film 11 can be formed to be thicker than the fluorine-based film 12, and a thickness accuracy (uniform thickness accuracy) of the composite film 11 is higher than that of the fluorine-based film 12. Therefore, even when the surface roughness of the metal member 10 is large in the first embodiment, by forming the thick composite film 11 on the metal member 10, the uneven surface of the metal member 10 is filled and smoothed with the composite film 11. Thus, the composite film 11 becomes a layer with a small surface roughness and the high thickness accuracy.
On the composite film 11, the fluorine-based film 12 is formed. The thickness of the fluorine-based film 12 can be made very thin, e.g., a few dozens nm. Therefore, the fluorine-based film 12 is easily affected by a surface roughness of the layer under the fluorine-based film 12. However, in the coating structure 1, the fluorine-based film 12 is formed on the composite film 11 with the small-surface roughness formed on the metal member 10. Therefore, even when the surface roughness of the metal member 10 is large in the first embodiment, the fluorine-based film 12 can be formed at a high accuracy without an effect due to the large surface roughness of the metal member 10. As a result, the fluorine-based film 12 becomes a uniform and high accuracy film without a sink.
As described above, in the coating structure 1 according to the first embodiment, the composite film 11, which can be formed to be thick, is formed on the metal member 10 as a first layer, and the thin fluorine-based film 12 is formed on the composite film 11 as a second layer. Therefore, the coating structure 1 can be used for the metal member 10 without being affect by the surface roughness of the metal member 10, even when the surface roughness of the metal member 10 is large. Thus, the metal member 10 is not required to be smoothed in advance until the surface roughness becomes an applicable surface roughness. Additionally, the coating structure 1 has the fluorine-based film 12 which is formed with the high accuracy on the metal member 10. Because the fluorine-based film 12 has the sufficient water-shedding property while having a uniform thickness, the coating structure 1 provides the sufficient water-shedding property and an antifouling property on the surface of the metal member 10.
The composite film 11 includes the NiP as the base material, and the NiP has a sufficient heat resistance. In the coating structure 1, the composite film 11 is formed between the metal member and the fluorine-based film 12. Therefore, even when the metal member 10 is heated, the water-shedding property of the fluorine-based film 12 is not reduced. Additionally, in the composite film 11, the water-shedding PTFE particles are dispersed in the NiP as the base material. Thus, the composite film 11 has the water-shedding property although the water-shedding effect is less than that of the fluorine-based film 12. Therefore, even when the fluorine-based film 12 is detached or deteriorated by heating or/and other reason, the composite film 11 prevents a substantial reduction of the water-shedding property of the coating structure 1.
The Ni strike film 13 is formed directly on the metal member 10. Therefore, the adhesiveness of the various films formed on the Ni strike film 13 can be improved. The composite film 11 is formed on the NiP film 14 that is applied on the Ni strike film 13. Therefore, the adhesiveness of the composite film 11 can be improved. Additionally, the composite film 11 is formed by the electroless plating. Therefore, the thickness accuracy of the composite film 11 can be improved.
The surface roughness of the surface, on which the composite film 11 is formed, i.e., the surface roughness Rz(14) of the NiP film 14 is as very small as about 0.03 μm. Therefore, the composite film 11 can be formed with the high accuracy. Additionally, the surface roughness Rz(11) of the composite film 11 is also as very small as about 0.03 μm. Therefore, the fluorine-based film 12 can be formed directly on the composite film 11 with the high accuracy. The fluorine-based film 12 includes the fluoroalkylsilane. Therefore, the fluorine-based film 12 has the sufficient water-shedding property.
In this way, the coating structure 1 according to the first embodiment can be used for the metal member 10 having the large surface roughness. The coating structure 1 has the sufficient water-shedding property which is not reduced by heating.
In the first embodiment, both the Ni strike film 13 and the NiP film 14 are formed between the metal member 10 and the composite film 11. However, according to a kind or a surface state of the metal member 10, the coating structure 1 may have both of the films 13 and 14, either of the films 13 or 14, or neither of the films 13 nor 14. For example, when a SCM420 is used as the metal member 10, both the Ni strike film 13 and the NiP film 14 are generally required. On the other hand, when a SPCC is used as the metal member 10, only the Ni strike film 13 is generally required. In each case, the coating structure 1 can be formed on the metal member 10 without being affected by the surface roughness of the metal member 10.
In the first embodiment, as a surface-smoothing layer for smoothing the surface of the metal member 10, the NiP/PTFE composite film 11 is used. However, a DLC (diamond-like carbon) can be used instead of the NiP/PTFE composite film 11. Because the DLC is a nonpolar material, the DLC film 11 may reduce an ion bonding with the foreign material. When the fluorine-based film 12 is formed on the DLC film 11, the surface of the fluorine-based film 12 becomes smooth, and an anchor effect based on the surface roughness is reduced. Therefore, the fluorine-based film 12 can prevent the adherence of the foreign material.
The DLC film 11 may be formed by a method selected from a plasma CVD, a sputtering, and an ion plating. In each case, the DLC film 11 can be formed with a high thickness accuracy.
A preferred thickness of the DLC film 11 is about in a range of 0.5 to 5 μm. When the thickness of the DLC film 11 is under 0.5 μm, the DLC film 11 may be not formed with the high accuracy on the metal member 10 having the large surface roughness, and a durability of the DLC film 11 may be reduced. When the thickness of the DLC film 11 is over 5 μm, it may be difficult to control the thickness of the DLC film 11.
A preferred surface roughness Rz of a surface, on which the DLC film 11 is formed, i.e., a surface roughness Rz of a layer under the DLC film 11, is not more than about 10 μm. When the surface roughness Rz is over 10 μm, the durability of the DLC film 11 may be reduced.
A preferred surface roughness Rz(11) of the DLC film 11 is not more than 10 μm. When the surface roughness Rz(11) is over 10 μm, the fluorine-based film 12 formed on the DLC film 11 may have a sink and may be not formed with the high accuracy.
The surface roughness Rz (11) of the DLC film 11 is smaller than the surface roughness Rz of the surface, on which the DLC film 11 is formed, because the surface is smoothed by forming the DLC film 11.
In a coating structure E according to a second embodiment of the invention, the NiP/PTFE composite film 11 is formed directly on the metal member 10, and the fluorine-based film 12 is formed on the composite film 11. The Ni strike film 13 and NiP film 14 described in the first embodiment are not formed in the second embodiment. In a coating structure C1 according to a first comparative example, only the fluorine-based film 12 is formed directly on the metal member 10. In a coating structure C2 according to a second comparative example, only the NiP/PTFE composite film 11 is formed directly on the metal member 10.
In each of the coating structures E, C1 and C2, the austenitic stainless steel (SUS304) is used as the material of the metal member 10 similarly to the first embodiment, and the surface roughness Rz(10) of the metal member 10 is 2 μm. Thicknesses and forming methods of the composite film 11 and the fluorine-based film 12 are similar to those of the first embodiment.
Next, water-shedding properties of the coating structures E, C1 and C2 are evaluated with a surface-free-energy measuring device (CA-VE type made by Kyowa Interface Science Co., Ltd) by measuring water contact angles in the conditions of φ0.7 mm of a syringe diameter, 3 to 4 μl of a measuring solution amount, θ/2 method, and a parallel contact angle.
The coating structure E according to the second embodiment includes both the fluorine-based film 12 having the sufficient water-shedding property, and the NiP/PTFE composite film 11 having the sufficient thermal resistance and the water-shedding property. Therefore, the coating structure E has the sufficient water-shedding property which is not reduced by heating.
In a third embodiment, a coating structure 1 similar to that of the first embodiment is used for a fuel injection nozzle 7. As shown in
The nozzle body 71 includes a guide hole 710 in which the needle 72 is inserted, a sliding hole part 711 adjacent to an opening end part 719 of the guide hole 710, a fuel storing part 712 provided in the guide hole 710, a fuel introducing passage 713 connected to the fuel storing part 712, a cone-shaped valve seat 715 located at a leading end part of the guide hole 710, and a plurality of injection holes 714 provided to penetrate through the valve seat 715.
The guide hole 710 is provided in the nozzle body 71 to extend in an axial direction. The fuel storing part 712 is provided by expanding an inside diameter of the guide hole 710 for all circumstances, and has a circular space on an outer peripheral side of the needle 72 inserted in the guide hole 710. The fuel introducing passage 713 is provided in the nozzle body 71 for introducing the high-pressure fuel, which has been supplied to the nozzle holder, to the fuel storing part 712.
The needle 72 includes a sliding part 723 inserted in the sliding hole part 711 so that the sliding part 723 is slidable, a cone-shaped valve part 721 for opening and closing the injection holes 714 by seating on and separating from the valve seat 715, a shaft part 722 for connecting the sliding part 723 and the valve part 721, and a journal part 724 on an axial end side of the sliding part 723.
An outside diameter of the shaft part 722 is smaller than that of the sliding part 723. The shaft part 722 is inserted in the guide hole 710 for forming a fuel passage 716 with the guide hole 710. In a part of the shaft part 722 against the fuel storing part 712, a pressure-receiving surface 725 and a small diameter part 726 are formed. The pressure-receiving surface 725 is formed to be taper-shaped in which a diameter becomes small from the side of the sliding part 723 to the small diameter part 726. A diameter of the small diameter part 726 is the smallest in the shaft part 722. The pressure-receiving surface 725 and the small diameter part 726 form the fuel storing part 712 with the nozzle body 71.
The nozzle body 71 is operated as described bellow. The high-pressure fuel is pumped by a fuel pump (not shown) through the fuel introducing passage 713, and is stored in the fuel storing part 712. When a fuel pressure of the fuel storing part 712 which is applied to the pressure-receiving surface 725 becomes higher than a pressure in a direction that the needle 72 closes a valve, the needle 72 is lifted-up by a predetermined amount in the guide hole 710. Thus, the valve part 721 is separated from the valve seat 715, the fuel passage 716 and the injection holes 714 are connected, and the high-pressure fuel is injected from the plurality of injection holes 714 into the cylinders of the engine. After that, when the fuel pressure applied to the pressure-receiving surface 725 becomes lower than a pressure in the direction that the needle 72 closes the valve, the needle 72 falls in the guide hole 710, the valve part 721 seats on the valve seat 715, the communication between the fuel passage 716 and the injection holes 716 is cut off, and the fuel injection is stopped.
In the fuel injection nozzle 7, the coating structure 1 according to the third embodiment of the invention is formed on a part of the needle 72. As shown in
As the surface-smoothing layer 11, the DLC film 11 is used. In the third embodiment, the DLC film 11 is formed on the area A1 of the needle 72, i.e., including the valve part 721, the shaft part 722, and the sliding part 723. The fluorine-based film 12 is formed on the area B1 of the needle 72, i.e., including the valve part 721 and the shaft part 722.
Therefore, the coating structure 1 is formed in an overlapped part in which the area A1 and the area B1 are overlapped. Here, on the area A1, the DLC film 11 is formed, and on the area B1, the fluorine-based film 12 is formed. On the sliding part 723 of the needle 72, only the DLC film 11 is formed. An abrasion resistance of the sliding part 723 is improved by a high-hardness and a high-solid lubrication property of the DLC film 11.
Next, a forming method of the DLC film 11 in the needle 72 will be described. In the third embodiment, the DLC film 11 is formed on a predetermined area of the needle 72 by a sputtering method. As shown in
After vacuating the coating apparatus 5 by the vacuum pump 52, argon gas 531 is introduced. The arc power source 57 supplies electricity to the filament electron source 59, so that the argon gas 531 becomes cations. When the bias power source 56 supplies a negative potential to the needle 72, the argon cations 531 hit against the needle 72, and a surface of the needle 72 is activated. When the sputter power source 51 supplies a negative voltage to the target 55, the argon cations 531 hit against the target 55 for taking out atoms 551. The atoms 551 pile-up on the needle 72 for forming the film. In this process, the needle 72 is located to be constantly rotated.
When a middle layer is formed, Cr (chrome), WC (tungsten carbide), Ti (titan), and Si (silicon) are used as the target 55, for example. When the DLC film 11 is formed, hydrocarbon gas is also introduced, and C (carbon) is used as the target 55, for example.
In the third embodiment, the sputtering is performed on the predetermined area of the needle 72 with three different targets 55, i.e., Cr (chrome), W (tungsten), and C (carbon), in this order. Eventually, the DLC film 11 including a Cr layer 111, a W/C layer 112, and a C layer 113 is formed as shown in
In the fuel injection nozzle 7, the coating structure 1 is formed on a part of the needle 72 (in the third embodiment, the valve part 721 and the shaft part 722, for example), on which the foreign material such as a product generated from fuel may adhere. The coating structure 1 has the sufficient water-shedding property which is not reduced by heating. Therefore, the coating structure 1 can prevent the foreign material from adhering and piling-up on the surface of the needle 72. Thus, the coating structure 1 can keep a good sliding condition of the needle 72, and the fuel injection nozzle 7 can inject fuel for long time.
In the third embodiment, the DLC film 11 is not formed on the journal part 724 of the needle 72. The journal part 724 is required to perform a gliding process for a dimensional coordination of the needle 72 after forming the DLC film 11. When the DLC film 11 is formed, the gliding process becomes difficult. Therefore, the DLC film 11 is not formed on the journal part 724. When the dimensional coordination is not required and the gliding process is not performed, the DLC film 11 may be formed on the journal part 724.
As shown in
As shown in FIGS. 6 and 9-11, the DLC film 11 may be formed on the area A1 or A2 in the needle 72 based on the situation. For example, in a new-development product, the DLC film 11 may be formed on the area A1 of the needle 72 because the DLC film 11 can be formed easily. However, in a conventional product which already has been used practically, the DLC film 11 is preferred to be formed on the area A2 of the needle 72, which excludes the valve part 721. In the conventional product, the valve part 721 may deteriorate with time because a friction is generated when the valve part 721 seats on and separates from the valve seat 715. Therefore, when the valve part 721 is checked, the valve part 721 may be optimized in accordance with a prediction of the deterioration. When the DLC film 11 is formed on the valve part 721, a pattern of the deterioration may be changed. Thus, when the valve part 721 is optimized similarly to the conventional case, a problem may be occurred. Therefore, in the conventional product, the DLC film 11 is formed on the area A2 in which the valve part 72 is excluded from the area A1.
In other words, in the third embodiment, the surface-smoothing layer 11 may be formed on the shaft part 722 and a part of the sliding part 723. Alternatively, the surface-smoothing layer 11 may be formed on the valve part 721, the shaft part 722, and a part of the sliding part 723. In each case, the surface of the needle 72 can be smoothed. Therefore, the fluorine-based film 12 formed on the surface-smoothing layer 11 becomes uniform without a sink, and can provide the sufficient water-shedding property which is not reduced by heating.
The fluorine-based film 12 may be formed on a part of the shaft part 722. Alternatively, the fluorine-based film 12 may be formed on the valve part 721 and a part of the shaft part 722. In each case, the fluorine-based film 12 can provide the sufficient water-shedding property on the predetermined portion of the needle 72.
The fluorine-based film 12 may be formed on an area which is not less than 80% of the shaft part 722. In this case, the fluorine-based film 12 can sufficiently prevent the needle 72 from adhering and piling-up of the foreign material such as the product generated from fuel.
Although the present invention has been fully described in connection with the preferred embodiments thereof with reference to the accompanying drawings, it is to be noted that various changes and modifications will become apparent to those skilled in the art.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-133845 | May 2006 | JP | national |
| 2007-050745 | Feb 2007 | JP | national |
