This application claims under 35 U.S.C. §119(a) priority to Korean Application No. 10-2008-0070306, filed on Jul. 18, 2008, the disclosure of which is incorporated herein by reference in its entirety.
1. Technical Field
The present invention relates to a valve lifter for an automotive internal combustion engine and a surface treatment method thereof.
2. Background Art
A valve lifter for converting the revolution of a camshaft into a vertical movement is mainly formed of alloy cast iron or carbon steel.
As shown in
However, the mirror surface finishing does not provide satisfactory surface roughness. The DLC or CrN coating shows low-friction characteristics. The DLC or CrN coating thus requires a specially designed oil to exhibit optimal low-friction characteristics, as disclosed in US Patent Application Publication No. 2005/0098134.
The above information disclosed in this the Background section is only for enhancement of understanding of the background of the invention and therefore it may contain information that does not form the prior art that is already known in this country to a person of ordinary skill in the art.
Accordingly, the present invention has been made keeping in mind the above problems occurring in the related art, and the present invention provides a valve lifter having superior low-friction characteristics, without the need to use a specially designed oil, and also provides a surface treatment method used in the manufacture of such a valve lifter.
According to one aspect of the present invention, a valve lifter may comprise a plurality of coating layers formed on the surface thereof to exhibit low-friction characteristics, wherein a top coating layer among the plurality of coating layers is a DLC layer having a SP3 bonding fraction of 60˜70%.
According to another aspect of the present invention, a valve lifter may a buffer layer formed by sputtering a metal target on a surface of the base body, which surface is subjected to carbonitriding treatment; an Me diamond-like carbon layer having a thickness of 0.3˜0.6 μm and formed by sputtering a target selected from the group consisting of W, Cr, Ti, and Mo on the buffer layer; and a diamond-like carbon layer formed on the Me diamond-like carbon layer, having a thickness of 1˜1.5 μm, and having a SP3 bonding fraction of 60˜70%.
Preferably, the base body, which is subjected to carbonitriding treatment, has a surface roughness (Ra) of 0.01˜0.04, and the buffer layer is a Cr coating layer formed by sputtering a Cr target.
Further, the DLC layer may have hydrogen content of 5˜15 wt % and a hardness of 28˜32 Gpa.
According to a further aspect, a method of treating the surface of the valve lifter may comprise: (a) carbonitriding and tempering a surface of a base body; (b) surface finishing the base body to produce a surface roughness (Ra) of 0.01˜0.04; (c) forming a metal buffer layer on the base body and then forming an Me diamond-like carbon layer with a thickness of 0.3˜0.6 μm on the metal buffer layer by sputtering a target selected from the group consisting of W, Cr, Ti, and Mo; and (d) forming a diamond-like carbon layer with a SP3 bonding fraction of 60˜70% and a thickness of 1˜1.5 μm on the Me diamond-like carbon layer.
The DLC layer may be formed by sputtering a graphite target, and the SP3 bonding fraction may be controlled by adjusting an amount of acetylene (C2H2) which is supplied and a magnitude of a bias voltage applied to a jig on which the valve lifter is to be mounted.
Preferably, the buffer layer is formed by sputtering a Cr target. Further, in the step (a), the tempering may be conducted at a temperature of 200˜250° C., and, in the steps (c) and (d), the coating layers are formed at a temperature maintained at 250° C. or lower.
Hereinafter, a detailed description will be given of a valve lifter and a surface treatment method thereof, with reference to the appended drawings.
As shown in
With reference to
First, the valve lifter is subjected to surface pretreatment before the surface thereof is coated.
For hardening and stabilization of the base body on which the coating layers are to be formed, carbonitriding is performed. That is, the surface of the base body is carbonitrided and then tempered at 200∞250° C. The surface of the base body which is carbonitrided is subjected to surface finishing to bring a surface roughness (Ra) to 0.01˜0.04 μm. If the surface roughness of the base body is less than 0.01 μm, the roughness is rather increased by the surface coating of the base body, undesirably resulting in excessive costs relative to produced effects. Conversely, if the surface roughness exceeds 0.04 μm, friction reduction effects are decreased due to the roughness of the coating layers. The surface finishing of the base body may be conducted through buffing, vibration finishing (VF), super finishing (SF), etc.
Next, the thus-obtained surface of the base body is coated.
In order to increase the force of adhesion of the base body to the coating layers formed thereon, a buffer layer is formed on the surface of the base body which is subjected to surface pretreatment. The buffer layer may be formed of Cr, Ti or the like. In particular, the effect of a Cr coating layer formed by sputtering a Cr target is better.
The surface of the base body having the buffer layer formed thereon is subjected to PACVD (Plasma Assisted Chemical Vapor Deposition) using acetylene as a carbon source, thus forming an Me-DLC layer. Specifically, the Me-DLC layer is formed by sputtering a metal target while supplying acetylene (C2H2) as a reactive gas to the surface of the base body. Examples of the metal target include W, Cr, Ti, and Mo. Particularly useful is W or Cr. The Me-DLC layer, functioning to increase impact resistance and the force of adhesion between the base body and the top DLC layer which exhibits low-friction characteristics, is deposited to a thickness of 0.3˜0.6 μm. If the thickness of the Me-DLC layer is less than 0.3 μm, impact resistance and force of adhesion are not adequately obtained. Conversely, if the thickness of the Me-DLC layer exceeds 0.6 μm, residual stress of the Me-DLC layer itself is increased, undesirably decreasing the effect of the Me-DLC layer.
On the Me-DLC layer, a DLC layer which actually exhibits low-friction characteristics is formed to a thickness of 1.0˜1.5 μm. If the thickness of the DLC layer is less than 1.0 μm, the DLC layer wears and disappears in the course of initial operation of an internal combustion engine. Conversely, if the thickness exceeds 1.5 μm, residual stress of the DLC layer itself is increased and thus the DLC layer peels off.
The DLC layer is formed by sputtering a graphite target while supplying acetylene. As shown in
The SP3 bonding fraction is controlled by precisely supplying acetylene and adjusting a bias voltage which is applied to a jig on which the valve lifter is mounted. The SP3 bonding fraction of the DLC layer is in proportion to an amount of hydrogen that is supplied and is in inverse proportion to a magnitude of a bias voltage. In consideration of only low-friction characteristics of the DLC layer, acetylene should be supplied in a small amount and a high bias voltage should be applied. However, the hardness of the DLC layer also depends on the bias voltage and is maximized at a specific bias voltage. Experimentally, only when the optimal value is obtained in joint consideration of the hardness and the SP3 bonding fraction, the DLC layer which is superior in both wear resistance and low-friction characteristics can be formed.
With reference to
In order to check the low-friction characteristics of the valve lifter coated by the above surface treatment method, six valve lifters formed of the same material were manufactured, each of which was subjected to surface treatment as shown in Table 1 below and then subjected to a friction torque test.
In Comparative Examples 1 and 2, only surface pretreatment was conducted, and in Comparative Examples 3 to 5 and Example of the present invention, surface pretreatment and multi-coating (buffer layer, Me-DLC layer, DLC layer) were conducted. The surface roughness of the base body and the SP3 bonding fraction of the DLC layer as a top coating layer, in Comparative Example 3, and the SP3 bonding fraction of the DLC layer in Comparative Examples 4 and 5, fell outside of the ranges according to the present invention. In the Example of the present invention, the valve lifter was manufactured within the ranges according to the present invention, and the SP3 bonding fraction of the DLC layer was 64%.
Each of the valve lifters of Comparative Examples 1 to 5 and the example was subjected to a rig test using an engine head system. The test conditions are shown in Table 2 below, and the test results are graphed in
In the graph of
Further, the valve lifter of the example was mounted to an actual engine, and a 500 hour durability test was conducted, after which wear scars of the surface of the valve lifter were observed. As is apparent from
As described above, the present invention provides a valve lifter and a surface treatment method thereof. According to the present invention, the valve lifter can exhibit superior low-friction characteristics, without the conventional need to use oil under specific conditions. Further, the valve lifter according to the present invention can manifest superior wear resistance.
Although the preferred embodiment of the present invention has been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.
Number | Date | Country | Kind |
---|---|---|---|
10-2008-0070306 | Jul 2008 | KR | national |
Number | Name | Date | Kind |
---|---|---|---|
6571865 | Shi et al. | Jun 2003 | B1 |
6844068 | Miyake et al. | Jan 2005 | B1 |
7255084 | Savale et al. | Aug 2007 | B2 |
20050098134 | Nishimura et al. | May 2005 | A1 |
20060207540 | Matsui et al. | Sep 2006 | A1 |
Number | Date | Country |
---|---|---|
2005-090489 | Apr 2005 | JP |
2007-0016818 | Feb 2007 | KR |
Number | Date | Country | |
---|---|---|---|
20100012064 A1 | Jan 2010 | US |