Patent Application
20210199158
The present invention relates to a sliding spline shaft device, and more specifically relates to a sliding spline shaft device unlikely to cause stick-slip.
A propeller shaft transmits output of an automobile engine to driving wheels. A propeller shaft is, for example, coupled to a transmission at one end and is also coupled to a differential gear at the other end, to transmit engine output to driving wheels.
In general, an engine and a differential gear are suspended to a vehicle body by elastic bodies, such as springs, and a distance between the engine and the differential gear varies due to acceleration and deceleration of an automobile. In view of this, the propeller shaft is provided with a sliding spline shaft device for absorbing the variation in the distance by sliding in an axial direction.
This sliding spline shaft device is required to smoothly slide in the axial direction and thus has a sliding surface that generates low friction force.
However, in the condition in which a dynamic friction force of the sliding surface is low, fast sliding occurs at the moment when stress acting on the sliding surface exceeds a static friction force, and the sliding ceases when the stress becomes low. As a result, the static friction force and the dynamic friction force alternately appear, that is, the so-called “stick-slip” occurs.
Japanese Unexamined Patent Application Publication No. 2013-189569 of Patent Document 1 discloses providing a coating film that contains solid lubricant, to suppress increase in static friction coefficient as well as suppress decrease in dynamic friction coefficient, whereby stick-slip is reduced.
Patent Document 1: JP2013-189569A
However, when torque acting on the sliding spline shaft device increases, the static friction force increases, whereby the difference between the static friction force and the dynamic friction force increases, resulting in generation of large vibration due to stick-slip.
The present invention has been made in view of such a problem of conventional art, and an object of the present invention is to provide a sliding spline shaft device that suppresses generation of vibration due to stick-slip even when a large torque is applied.
The inventors of the present invention have made an intensive research to achieve the above object and have found the following findings. That is, the above object can be achieved by increasing hardness of a surface of a base material to reduce microscopic deformation of a sliding surface and thereby suppressing increase in real contact area. Thus, the present invention has been completed.
Specifically, a sliding spline shaft device of the present invention includes a male spline and a female spline that is fitted to the male spline in an axially slidable manner, and at least one of the splines has a surface processed layer.
The surface processed layer includes an undercoat layer, an intermediate layer containing phosphate, and a topcoat layer containing solid lubricant, in this order. The undercoat layer contains iron nitride and/or iron carbide.
In the present invention, the surface hardness of the base material of the spline is increased to reduce microscopic deformation of the sliding surface. Thus, the present invention provides a sliding spline shaft device that is unlikely to cause stick-slip even when a large torque is applied.
A sliding spline shaft device of the present invention will be described in detail. As illustrated in
As illustrated in
Undercoat Layer
The undercoat layer contains iron nitride and/or iron carbide and hardens the surface of the base material.
The undercoat layer preferably has Vickers hardness (HV) of 500 HV0.1 or greater. The undercoat layer, which has Vickers hardness of 500 HV0.1 or greater, suppresses microscopic deformation of the sliding surface and thereby prevents increase in static friction coefficient due to stress.
The upper limit of Vickers hardness (HV) is not specifically limited, but the practical upper limit of hardness is 900 HV0.1 or less in a case of hardening the base material to be used in the sliding spline shaft device.
Note that Vickers hardness (HV) can be measured in accordance with JIS Z 2244. In addition, the numerical value that is suffixed to “HV” represents a load in measurement of Vickers hardness, in unit of kg. That is, “HV0.1” represents a measurement under a load of 0.1 kg.
The undercoat layer can be formed by nitriding or carburizing, but is preferably formed by nitriding. An undercoat layer that is formed by nitriding has high tempering resistance and is thereby not prone to cause decrease in surface hardness in forming the intermediate layer, which will be described later.
Examples of a method of the nitriding include a salt-bath nitrocarburizing method, a gas nitrocarburizing method, and an ion nitriding method. These nitriding treatments enable forming an undercoat layer at a temperature of an A1 transformation point of the base material or less, whereby strain deformation of the base material is suppressed.
The undercoat layer that is formed by nitriding has a diffusion layer and a compound layer, in this order, from the base material side. The diffusion layer is a layer, in which nitrogen is diffused in the base material. The compound layer is columnar crystals containing Fe2-3N and Fe4N.
Among them, a compound layer that is formed by a salt-bath nitrocarburizing method is porous and improves peeling resistance of the intermediate layer (described later) by an anchoring effect, more than a compound layer that is formed by an ion nitriding method or a gas nitrocarburizing method. Moreover, this compound layer is well lubricated with lubricating oil even when lubricating layers, e.g., the intermediate layer and the topcoat layer, are worn out, and thus, this compound layer improves wear resistance.
The thickness of the compound layer is preferably 5 μm or greater and 15 μm or less. When the compound layer is very thin, deformation of the sliding surface may not be sufficiently suppressed. When the compound layer is very thick, the compound layer is embrittled, and a static friction force may increase.
The diffusion layer is a layer in which nitrogen is diffused in a sorbite structure of the base material to generate nitrides, such as Al—N, Cr—N, and Mo—N. The nitrides generate strain in the crystal lattice of Fe and hardens the surface of the base material.
The diffusion layer has high affinities with the base material and the compound layer and prevents peeling off of the compound layer as well as improves fatigue strength of the base material.
In a case in which the surface hardness of the base material is sufficiently high, it is not necessary to form the undercoat layer to each of the male spline and the female spline, and the undercoat layer may be formed only to the spline that has a base material with a lower surface hardness.
Intermediate Layer
The intermediate layer contains phosphate and improves wear resistance as well as adhesion of the topcoat layer, which will be described later.
The intermediate layer can be formed by phosphating. Examples of the phosphating include a zinc phosphate treatment, a manganese phosphate treatment, and a calcium phosphate treatment. Among them, the manganese phosphate treatment is preferable for forming the intermediate layer.
A manganese phosphate crystal that is formed by a manganese phosphate treatment tends to be larger than crystals that are formed by other phosphate treatments, and the manganese phosphate crystal forms an intermediate layer having a high maximum height (Ry). Thus, the manganese phosphate crystal improves peeling resistance of the topcoat layer by an anchoring effect. The topcoat layer will be described later.
Moreover, manganese phosphate makes the sliding surface smooth due to self-sacrificial wear and reduces surface pressure, thereby improving wear resistance.
The film thickness of the intermediate layer is preferably 1 μm or greater and 5 μm or less.
When the film thickness is less than 1 μm, wear resistance may not be sufficiently improved. On the other hand, when the film thickness exceeds 5 μm, due to the intermediate layer that is softer than the undercoat layer, a real contact area may increase to cause increase in static friction force when a large torque is applied to the sliding surface.
Topcoat Layer
The topcoat layer contains solid lubricant and binder resin and reduces a dynamic friction force even when a large torque is applied to the sliding surface and breaks an oil film, and a mixed lubrication state or a boundary lubrication state occurs.
The solid lubricant may use inorganic fine particles or organic fine particles. Examples of the inorganic fine particles include inorganic fine particles of metal sulfides, e.g., molybdenum disulfide, graphite, carbon black, boron nitride, and metal oxides. On the other hand, examples of the organic fine particles include organic fine particles of fluororesin, polyolefin, and polyamide. These materials may be used alone or in combination.
Among them, the molybdenum disulfide particles and the graphene particles have lamellar structures in which thin pieces are laminated on one after another, and therefore, they have high load bearing performances and decrease a dynamic friction force by being dislocated in a certain direction when receiving a load. Thus, molybdenum disulfide particles and graphene particles are preferably used.
An average particle size (Fisher method) of the solid lubricant is preferably 0.3 μm or greater and 3 μm or less. In the condition in which the solid lubricant has particle sizes in the above range, a topcoat layer with a thin film thickness can be formed.
The amount of the solid lubricant in the topcoat layer is preferably 15 mass % or greater and 45 mass % or less.
Examples of the binder resin include polyamide-imide resin, polyphenylene sulfide resin, epoxy resin, phenol resin, and modified resins thereof. Among them, the polyamide-imide resin and the modified resin thereof have superior wear resistance and are thus preferably used.
The topcoat layer can be formed, for example, by applying polyamic acid solution that contains solid lubricant, drying it to remove solvent, and performing imidization reaction.
Any solvent in which polyimide dissolves without generating a gel product and a precipitate, can be used as the solvent of the polyimide solution. For example, organic polar solvent, such as formamide solvent, acetamide solvent, and pyrrolidone solvent, may be used. These solvents may be used alone or several types of the solvents may be used as a mixed solvent.
The polyamic acid solution may further contain an additive, such as surface active agent or anti-settling additive. Surface active agent that is added, uniformly disperses the solid lubricant in the polyamic acid solution and maintains the dispersed state.
The film thickness of the topcoat layer is preferably 1 μm or greater and 15 μm or less and more preferably 1 μm or greater and 9 μm or less.
When the film thickness is less than 1 μm, a dynamic friction force may not be sufficiently reduced. On the other hand, when the film thickness exceeds 15 μm, due to the topcoat layer that is softer than the undercoat layer, a real contact area may increase to cause increase in static friction force when a large torque is applied to the sliding surface.
Moreover, an average of the total film thickness of the intermediate layer and the topcoat layer is preferably 20 μm or less, more preferably, 15 μm or less, and further preferably, 10 μm or less.
When the total film thickness of the intermediate layer and the topcoat layer is 20 μm or less, minute deformation of the sliding surface is suppressed in conjunction with the undercoat layer, whereby increase in static friction force is suppressed even when a large torque is applied to the sliding surface.
The film thicknesses of the topcoat layer, the intermediate layer, and the undercoat layer can be measured by analyzing a cross-sectional SEM image of the surface processed layer.
In the present invention, a film thickness at an intermediate point on a waveform-shaped inclined surface of the spline is measured at ten positions, and the results are averaged to obtain an average film thickness.
Base Material
The base material may use a steel material that is conventionally used for a sliding spline.
Specifically, it is possible to use a carbon steel containing 0.18 mass % or greater and 0.48 mass % or less of carbon (C), 0.15 mass % or greater and 0.35 mass % or less of silicon (Si), and 0.60 mass % or greater and 0.90 mass % or less of manganese (Mn).
The present invention will be detailed with reference to Examples hereinafter, but the present invention is not limited to Examples described below.
An S45C flat test piece (female spline, hardness: 260 HV0.1) and an Scr420H columnar test (male spline, 6 mm in diameter and 12 mm in height, hardness: 650 HV0.1) were degreased and washed by alkali solution and were dried, and they were preheated to approximately 350° C. and were then immersed in a molten salt bath at 570° C. for 90 minutes to be subjected to salt-bath nitrocarburizing (ISONITE (registered trademark) treatment, manufactured by Nihon Parkerizing Co., Ltd.).
Each of these test pieces was then taken out of the bath, cooled at a room temperature, and washed by water. Thus, an undercoat layer including a compound layer that had a film thickness of 9 μm, was formed.
The surface hardness (HV) of the S45C female spline test piece was 650 HV0.1, and the surface hardness (HV) of the Scr420H male spline test piece was 800 HV0.1.
(Formation of Intermediate Layer)
Each of the test pieces that were formed with the undercoat layer was immersed in a manganese phosphate treatment liquid (“PALFOS MiA”, manufactured by Nihon Parkerizing Co., Ltd.) at approximately 100° C. for 10 minutes, washed, and then dried, whereby an intermediate layer with a film thickness of 2 μm was formed.
(Formation of Topcoat Layer)
Each of the test pieces that were formed with the intermediate layer was coated with a molybdenum disulfide solid lubricant coating material (“Defric Coat”, HMB-2H2, manufactured by Kawamura Research Lab., Inc.) by spraying and was dried at 180° C. for 30 minutes under nitrogen atmosphere, whereby solvent was removed. Thereafter, each of the test pieces was heated at 250° C. for 2 hours, whereby polyamide-imide resin containing molybdenum disulfide formed a topcoat layer having a thickness of 7 μm. Thus, test pieces of a sliding spline device were prepared. A cross-sectional SEM image of the test piece is illustrated in
A test piece of the sliding spline device was prepared in the same manner as in Example 1, except for forming a topcoat layer having a film thickness of 13.5 μm.
A test piece of the sliding spline device was prepared in the same manner as in Example 2, except for not forming an undercoat layer.
Evaluation
Static friction force and dynamic friction force were measured with respect to each varied load in the condition in which a reciprocation frequency of 3 Hz and an amplitude of 2.2 mm, by using a high-speed reciprocating friction test apparatus (PLINT TE77).
Measurement results of dynamic sliding force, measurement results of static sliding force, and a difference between the static sliding force and the dynamic sliding force, are illustrated in
As illustrated in
Moreover, as illustrated by the graph of the difference between the static sliding force and the dynamic sliding force in
Furthermore, static friction coefficient and dynamic friction coefficient of each of Examples 1 and 2 were measured.
The measurement results are illustrated in Table 1.
The result of Table 1 shows that Example 1, which had the topcoat layer with the film thickness of 7 μm, had smaller static friction coefficient than Example 2, which had the topcoat layer with the film thickness of 13.5 μm, and stick-slip can be prevented, because the ratio of the static sliding force and the dynamic sliding force is small.
(Durability Test)
Durability test was performed by sliding repeatedly under a fixed load of 100 N in the condition in which a reciprocation frequency of 3 Hz and an amplitude of 2.2 mm, by is using the high-speed reciprocating friction test apparatus (PLINT TE77).
The test result of Example 1 is illustrated in
A comparison between the graph in
The reason for this is that minute deformation of the sliding surface is suppressed, the topcoat layer and the intermediate layer are not prone to wear, and furthermore, the undercoat layer is hard such that the base metal in the base material is unlikely to be exposed even when the topcoat layer and the intermediate layer are worn out.
Table 1 and
| Number | Date | Country | Kind |
|---|---|---|---|
| 2018-098939 | May 2018 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2019/015959 | 4/12/2019 | WO | 00 |
