• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    PURPOSE: A surface treatment process for mechanical parts subject to wear and corrosion is provided to obtain high wear and corrosion resistance and a roughness propitious to lubrication by carrying out the nitriding and oxidation operations in particular baths. CONSTITUTION: In a surface treatment process for mechanical parts, for conferring on said parts a high resistance to wear and corrosion and a roughness propitious to lubrication, in which process nitriding of said part is followed consecutively by oxidation of said part, said nitriding is applied by immersing said part in a molten salt nitriding bath free of sulfur-containing species at a temperature from approximately 500 deg.C. to approximately 700 deg.C., and said oxidation is carried out in an oxidizing aqueous solution at a temperature less than approximately 200 deg.C.
    公开号:KR20020013797A
    申请号:KR1020010048641
    申请日:2001-08-13
    公开日:2002-02-21
    发明作者:쵸머스테판；테일스테판
    申请人:쥐. 엘 뽈띠；쌍트르 스테파느와 드 르쉑슈 메까니끄 이드로메까니끄 에 프로뜨망；
    IPC主号:
    专利说明:

    A SURFACE TREATMENT PROCESS FOR MECHANICAL PARTS SUBJECT TO WEAR AND CORROSION
    [1] The present invention relates to a method for treating a surface of a mechanical part that is susceptible to wear and corrosion. More specifically, the present invention relates to a method for surface treatment of a mechanical part susceptible to wear and corrosion, which gives the mechanical part a high resistance to wear and corrosion and a good roughness to lubricate. More precisely, the present invention relates to a method for treating a surface of a machine part in which lubrication must be precisely controlled and, as a result, the roughness must be controlled within a narrow range.
    [2] As is well known in the art, the thickness of the oil film on the surface of a part depends largely on the roughness of its surface. That is, a fully polished part will not be wetted by oil, while conversely, a very rough part will be covered with a film whose thickness is less than the height of the micro relief, thus increasing the risk of bonding.
    [3] Parts that can be advantageously treated according to the invention include, for example, piston rods and internal combustion engine valves. As for the piston rod, the thickness of the oil film on its surface must be fully controlled; If it is too thin, the rod-seal contact is no longer lubricated and wear occurs; If it is too thick, the resulting leakage of lubricant will degrade performance.
    [4] As for the internal combustion engine valve, the oil film performs lubrication and dynamic sealing function at the contact surface between the valve stem and the valve guide; Too highly polished parts will produce a thin oil film, lubrication will be random, while high roughness will result in high oil consumption and loss of engine efficiency.
    [5] When facing members that must withstand wear and corrosion, there will be many solutions to those skilled in the art. Therefore, it is standard to use a thick coating of "hard chromium" with microcracks It is customary. However, these coatings have drawbacks. From a technical point of view, the presence of an interface between steel and chromium can cause dramatic scaling in the intended function; Moreover, in the case of intermittent working parts such as certain piston-and-cylinder arrangements, there is a risk of removal of residual lubricant film due to severe weather and the resulting corrosion. From an economic point of view, the method requires metal coating and then machining to make it an expensive solution. Finally, from an environmental point of view, chromium plating is very widely carried out using a bath containing chromium VI as the main pollutant.
    [6] Another widely used solution is to nitrate the part and then to oxidize it; These two operations often lead to the impregnation of the surface holes with a product which further improves the corrosion resistance. The operation is carried out continuously, for example in a salt bath as disclosed in French patent FR-A-2 672 059 or FR-A-2 679 258, or in a gas atmosphere as disclosed, for example, in European patent 0217420.
    [7] The combination of nitriding and oxidation generally confers high resistance to wear and corrosion, but systematically increases the surface roughness of the part to a degree not consistent with that required for the application to which the present invention relates.
    [8] This increase in roughness allows a person skilled in the art to apply the process a rather extensive polishing of one or more steps resulting in a sequence such as nitriding-oxidation-polishing or even nitriding-oxidation-polishing-oxidation. These types of methods perform lubrication efficiently, but are difficult to use industrially because they require a combination of different techniques (thermochemical and mechanical) that make them very expensive and of limited use; It is difficult to control the roughness of a complicated part by polishing.
    [9] Surprisingly, the applicant has shown that it is possible to achieve high wear resistance and corrosion resistance and good roughness by lubricating by performing nitriding and oxidation in a particular bath.
    [10] The above stated purpose is high resistance to wear and corrosion on mechanical parts And a method of treating a surface of a mechanical component following oxidation of the component subsequent to nitriding of the component, which gives a good roughness for lubrication, wherein the nitriding is a sulfur-free paper-free molten salt at a temperature of about 500 ° C. to about 700 ° C. By immersing the component in a nitriding bath, and the oxidation is satisfied by the present invention, which is carried out in an oxidizing aqueous solution at a temperature of less than approximately 200 ° C.
    [11] In order to be in accordance with the invention, the process must also be subject to a continuous combination of nitriding and oxidation, with both operations carried out in the liquid phase under the conditions specified above.
    [12] However, it is not a matter of a continuous combination of specific nitriding processes and specific oxidation processes, but rather of an inseparable combination of nitriding and oxidation processes because there is a very high level of interaction between them in the process according to the invention.
    [13] Two steps of the process, the nitriding step and the oxidation step, should be subject to the following conditions:
    [14] (1) The first step (nitriding operation) should be carried out in a molten bath without sulfur containing species.
    [15] The temperature of the bath is about 500 ° C to about 700 ° C, such as about 590 ° C to about 650 ° C.
    [16] Advantageously, the bath comprises alkali carbonate and alkali cyanate and has the following composition:
    [17] Li + = 0.2-10 wt%
    [18] Na + = 10-30 wt%
    [19] K + = 10-30 wt%
    [20] CO 3 2- = 25-45 wt%
    [21] CNO - = 10 - 40 wt%
    [22] CN - <0.5% by weight
    [23] For example, the molten salt nitridation bath contains the following ions with ions of CN − in an amount of up to 0.5% by weight:
    [24] Li + = 2.8-4.2 wt%
    [25] Na + = 16.0-19.0 wt%
    [26] K + = 20.0-23.0 wt%
    [27] CO 3 2- = 38.0-43.0 wt%
    [28] CNO - = 12.0 - 17.0 wt%
    [29] Agitation with compressed air is advantageously provided.
    [30] Advantageously, the time of immersion of the part is at least about 10 minutes; Extended to several hours as required. Immersion times of the parts are usually from about 30 minutes to about 60 minutes.
    [31] (2) After nitriding, the second step (oxidation operation) should be carried out at a temperature of less than approximately 200 ° C. Preferably, the temperature of the oxidation bath is about 110 ° C to about 160 ° C. More preferably, the temperature of the oxidation bath is from about 125 ° C to about 135 ° C.
    [32] Advantageously, the composition of the bath is as follows:
    [33] OH - = 10.0 - 22% by weight
    [34] NO 3 - = 1.8 - 11.8% by weight
    [35] NO 2 - = 0 - 5.3 wt%
    [36] S 2 O 3 2- = 0.1-1.9 wt%
    [37] Cl - = 0 - 1.0 wt%
    [38] Na + = 1.0-38 wt%
    [39] For example, the oxidizing aqueous solution contains the following ions:
    [40] OH - = 17 - 18.5% by weight
    [41] NO 3- = 4.0-5.5 wt%
    [42] NO 2 - = 1.0 - 2.5% by weight
    [43] Cl - = 0.25 - 0.35% by weight
    [44] Na + = 25-29 wt%
    [45] For example, the aqueous oxidation solution further contains 0.6 to 1.0 wt% of thiosulfate ion S 2 O 3 2- .
    [46] Advantageously, the immersion time of the part in the oxidation bath is from about 5 minutes to about 45 minutes.
    [47] It is noteworthy that after nitriding and subsequent oxidation according to the present invention, the parts treated afterwards can be effectively impregnated as in the prior art. Although the final roughness is much lowered, the affinity of the layer for the impregnation product is, however, high . This amazing fact has not yet been scientifically explained.
    [48] The present invention also provides a component treated by the above method of causing surface deformation. The part according to the invention is characterized in that its roughness R a has a value of less than approximately 0.5 μm and its surface is free of “tables”.
    [49] The invention is described in more detail below by the following non-limiting examples.
    [50] (Example 1)
    [51] Both parallelepiped samples with dimensions of 30 × 18 × 8 mm of non-alloy steels containing 0.35% carbon and having an initial roughness R max = 0.6 μm, followed by a 19 mm by weight of cyanate ion, 37 with a 35 mm diameter ring, 37 It contained a wt% carbonate ion and 3.5 wt% lithium ions, the remainder being treated in a nitriding salt bath consisting of sodium and potassium ions. The part was immersed at 630 ° C. for 40 minutes.
    [52] When removed from the bath, the parts were cooled in a water tank and then washed to soak for 15 minutes in 135 ° C. oxidized saline consisting of 85 kg of the next salt mixture (see Table 1) per 75 liters of water.
    [53]
    [54] The parts are then washed in water at 80 ° C. and then soluble in 40 ° C. Neutralize in solution and dry.
    [55] Samples were characterized by measuring their roughness and by friction test.
    [56] The measured roughness of the components treated as above is shown in Table 2, which corresponds to the standard methods N1, N2, Ox1 and Ox2, N1 corresponding to nitriding according to FR 72 05 498, N2 corresponding to nitriding according to (TF1). , Ox1 corresponding to oxidation by FR 93 09814 and Ox2 corresponding to oxidation by FR 76 07858. The shape parameters of the roughness pattern used to define the surface condition are denoted by R a (length arithmetic mean) and R (depth axle average).
    [57]
    [58] Note that the method according to the invention obtains roughness equivalent to that of the conventional method followed by grinding.
    [59] For the friction test, the rings were pressed against the large face of the plate at a regularly increasing load from an initial value of 5 daN and at a constant sliding speed of 0.55 m / s. The abrasive surface of the plate was greased before testing. The results are shown in Table 3.
    [60]
    [61] (Example 2)
    [62] A cylinder of high alloy steel containing 0.45% carbon, 9% chromium and 3% silicon was treated in a nitriding bath having exactly the same composition as that of Example 1.
    [63] The part was immersed in a bath maintained at a temperature of 590 ° C. for 30 minutes and then quenched with cold water. After washing them, they were oxidized at 130 ° C. for 10 minutes in the brine described in Example 1 and then washed again with hot water.
    [64] With this type of steel, the roughness obtained by the standard carburization + oxidation or sulfocarburization + oxidation process was relatively high due to the poor quality (many porous layers and poor adhesive oxide powder) of the surface layer obtained. For example, RzThe value of is usually similar to 10 μm and roughness R around 2 μm by grinding operation or even micro shot blasting.zTo reduce Often needed
    [65] Samples treated under the conditions specified for this example had a roughness R z of 2 to 2.5 μm without requiring any polishing or microshot blasting.
    [66] Note: R z is the average roughness depth according to the French standard NF ISO 4287 of 1997 corrected in 1 998.
    [67] (Example 3)
    [68] The test was carried out to show the extent to which the method according to the invention constitutes an inseparable combination. Cylindrical samples of non-alloy steels containing 0.35% by weight carbon were treated by combining conventional oxidation methods with various nitriding methods, including those quoted in Examples 1 and 2.
    [69] The nitriding step consists of 37% by weight of cyanate ions and 17% by weight of carbonate ions, the remainder being alkaline K + , Na + and Li + cations, further in a salt bath having 10 to 15 ppm of S 2- ions It was carried out at 570 ° C. according to FR 72 05498 or under the same conditions as those in Example 1.
    [70] The oxidation step is based on 13.1% by weight carbonate ions, 36.5% by weight nitrate ions, 11.3% by weight hydroxide ions and 0.1% by weight dichromate ions and in a salt bath with alkali K + , Na + and Li + cations, 475 In accordance with FR 9309814 or under the conditions described in Examples 1 and 2.
    [71] The roughness results obtained are shown in Table 4 below; Initial roughness R a of all the samples was 0.3 micrometer.
    [72]
    [73] The surface treatment method of the present invention imparts high wear resistance and corrosion resistance and good roughness to lubrication of mechanical parts that are susceptible to wear and corrosion.
    权利要求:
    Claims (15)
    [1" claim-type="Currently amended] High resistance to wear and corrosion on mechanical parts And a method of treating a surface of a mechanical component following oxidation of the component subsequent to nitriding of the component, which gives a good roughness for lubrication, wherein the nitriding is a sulfur-free paper-free molten salt at a temperature of about 500 ° C. to about 700 ° C. Performing by immersing the component in a nitriding bath, and the oxidation is carried out in an oxidizing aqueous solution at a temperature of less than approximately 200 ° C.
    [2" claim-type="Currently amended] The method according to claim 1, wherein the molten salt nitridation bath contains the following ions together with ions of CN − in an amount of 0.5% by weight or less.
    Li + = 0.2-10 wt%
    Na + = 10-30 wt%
    K + = 10-30 wt%
    CO 3 2- = 25-45 wt%
    CNO - = 10 - 40 wt%
    [3" claim-type="Currently amended] The method according to claim 2, wherein the molten salt nitridation bath contains the following ions together with ions of CN − in an amount of 0.5% by weight or less.
    Li + = 2.8-4.2 wt%
    Na + = 16.0-19.0 wt%
    K + = 20.0-23.0 wt%
    CO 3 2- = 38.0-43.0 wt%
    CNO - = 12.0 - 17.0 wt%
    [4" claim-type="Currently amended] The method of claim 1, wherein the machine part is immersed in a nitriding bath for at least about 10 minutes.
    [5" claim-type="Currently amended] 5. The method of claim 4 wherein the machine part is immersed in a nitriding bath for about 30 to about 60 minutes.
    [6" claim-type="Currently amended] The method according to any one of claims 1 to 5, wherein the nitriding bath is stirred with compressed air.
    [7" claim-type="Currently amended] The method according to any one of claims 1 to 6, wherein the aqueous oxidation solution contains the following ions.
    OH - = 10.0 - 22% by weight
    NO 3 - = 1.8 - 11.8% by weight
    NO 2 - = 0 - 5.3 wt%
    Cl - = 0 - 1.0 wt%
    Na + = 1.0-38 wt%
    [8" claim-type="Currently amended] 8. The method according to claim 7, wherein the aqueous oxidation solution contains the following ions.
    OH - = 17 - 18.5% by weight
    NO 3- = 4.0-5.5 wt%
    NO 2 - = 1.0 - 2.5% by weight
    Cl - = 0.25 - 0.35% by weight
    Na + = 25-29 wt%
    [9" claim-type="Currently amended] The method according to any one of claims 1 to 8, wherein the aqueous oxidation solution further contains 0.1 to 1.9 wt% of thiosulfate ion S 2 O 3 2- .
    [10" claim-type="Currently amended] The method according to claim 9, wherein the aqueous oxidation solution further contains 0.6 to 1.0 wt% of thiosulfate ion S 2 O 3 2- .
    [11" claim-type="Currently amended] The process according to claim 1, wherein nitriding is carried out at a temperature of about 590 ° C. to about 650 ° C. 12.
    [12" claim-type="Currently amended] The process according to claim 1, wherein the oxidation is carried out at a temperature of about 110 ° C. to about 160 ° C. 12.
    [13" claim-type="Currently amended] 13. The method of claim 12, wherein the oxidation is carried out at a temperature of about 125 ° C to about 135 ° C.
    [14" claim-type="Currently amended] The method of claim 1, wherein the part is immersed in the oxidation bath for about 5 minutes to about 45 minutes.
    [15" claim-type="Currently amended] The method according to any one of claims 1 to 14, which induces surface deformation, characterized in that the roughness R a has a value of less than approximately 0.5 μm and its surface is free of “tables”. Processed parts.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-08-14|Priority to FR0010633A
    2000-08-14|Priority to FR0010633
    2001-08-13|Application filed by 쥐. 엘 뽈띠, 쌍트르 스테파느와 드 르쉑슈 메까니끄 이드로메까니끄 에 프로뜨망
    2002-02-21|Publication of KR20020013797A
    2004-12-03|Application granted
    2004-12-03|Publication of KR100458663B1
    优先权:
    申请号 | 申请日 | 专利标题
    FR0010633A|FR2812888B1|2000-08-14|2000-08-14|Process for the surface treatment of mechanical parts subject to both wear and corrosion|
    FR0010633|2000-08-14|
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