EP0638661B1 - Procédé pour améliorer la résistance à l'usure et à la corrosion de pièces en métaux ferreux - Google Patents
Procédé pour améliorer la résistance à l'usure et à la corrosion de pièces en métaux ferreux Download PDFInfo
- Publication number
- EP0638661B1 EP0638661B1 EP94401716A EP94401716A EP0638661B1 EP 0638661 B1 EP0638661 B1 EP 0638661B1 EP 94401716 A EP94401716 A EP 94401716A EP 94401716 A EP94401716 A EP 94401716A EP 0638661 B1 EP0638661 B1 EP 0638661B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bath
- parts
- salts
- oxygenated
- corrosion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 22
- 230000007797 corrosion Effects 0.000 title claims description 31
- 238000005260 corrosion Methods 0.000 title claims description 31
- 229910052751 metal Inorganic materials 0.000 title claims description 11
- 239000002184 metal Substances 0.000 title claims description 11
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 title claims description 8
- 230000008569 process Effects 0.000 title abstract description 14
- 150000003839 salts Chemical class 0.000 claims abstract description 35
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims abstract description 11
- 150000002823 nitrates Chemical class 0.000 claims abstract description 11
- 238000005121 nitriding Methods 0.000 claims abstract description 10
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 9
- 238000009792 diffusion process Methods 0.000 claims abstract description 9
- 150000004679 hydroxides Chemical class 0.000 claims abstract description 7
- 159000000000 sodium salts Chemical class 0.000 claims abstract description 5
- 238000005256 carbonitriding Methods 0.000 claims abstract description 4
- 125000000129 anionic group Chemical group 0.000 claims abstract description 3
- 239000007788 liquid Substances 0.000 claims abstract description 3
- 150000001450 anions Chemical class 0.000 claims abstract 2
- -1 alkali metal salts Chemical class 0.000 claims description 11
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 claims description 4
- 238000007654 immersion Methods 0.000 claims description 4
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 claims description 3
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 claims description 3
- 150000004978 peroxycarbonates Chemical class 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 abstract description 5
- 229910000288 alkali metal carbonate Inorganic materials 0.000 abstract 1
- 150000008041 alkali metal carbonates Chemical class 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 21
- 230000001590 oxidative effect Effects 0.000 description 21
- 239000000203 mixture Substances 0.000 description 17
- 238000012360 testing method Methods 0.000 description 17
- 238000007254 oxidation reaction Methods 0.000 description 11
- 230000003647 oxidation Effects 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 6
- 230000006872 improvement Effects 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 5
- 150000004767 nitrides Chemical class 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910000851 Alloy steel Inorganic materials 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 230000003313 weakening effect Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000001594 aberrant effect Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 150000001913 cyanates Chemical class 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical class Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 229940082150 encore Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/40—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions
- C23C8/42—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions only one element being applied
- C23C8/48—Nitriding
- C23C8/50—Nitriding of ferrous surfaces
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/70—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using melts
- C23C22/72—Treatment of iron or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/80—After-treatment
Definitions
- the present invention relates to a method for improving the resistance to wear and corrosion of ferrous metal parts, making it possible to guarantee a high degree of reproducibility of the results whatever the type of parts treated.
- thermochemical diffusion treatments and in particular those designated by nitriding, is known for improving the wear resistance of ferrous metal parts.
- Patent FR 2 306 268 from 1976 describes an oxidizing salt bath composed of alkali hydroxides, optionally with an alkali nitrate in an amount of 2 to 20% by weight.
- This salt bath at preferred operating temperatures of 200 to 300 ° C, is essentially intended to simultaneously achieve controlled cooling of ferrous metal parts nitrides, leaving a cyanate / cyanide nitriding bath, and the destruction by oxidation of the cyanides entrained by the parts.
- Patent FR 2,525,637 of 1982 describes a process for treating ferrous metal parts in an oxidizing salt bath to improve their resistance to corrosion, parts containing sulfur.
- This document teaches to immerse the parts in an oxidizing bath, comprising alkali hydroxides, nitrates and / or alkali nitrites and possibly alkali carbonates, with in addition from 0.5 to 15% by weight of a strong oxidant, in the species of oxygenated alkali metal salts whose normal redox potential compared to the hydrogen reference electrode is less than or equal to - 1 volt.
- Bichromates, permanganates, peroxycarbonates, iodates and periodates are cited as oxygenated salts, the alkali metals being sodium and potassium.
- the process described in this patent is further characterized in that an oxygen-containing gas is injected into the salt bath and in that the weight content of the bath in insoluble particles is kept at less than 3%.
- This process provides even better performance. It not only improves the corrosion resistance of the parts this time by a factor of almost 4, but also does not alter their resistance to wear and fatigue and even improve their anti-seizure properties in dry friction.
- EP-A-0 497 663 describes a process aimed at improving the corrosion resistance of ferrous metal parts which have undergone nitriding and oxidation in a bath corresponding to the teaching of FR-A-2 525 637, by depositing on the surface of the treated parts, a coating of a polymer, for example FEP (fluoroethylene-propylene), having a thickness of 3 to 20 ⁇ m.
- FEP fluoroethylene-propylene
- the subject of the present invention is a process, associating thermochemical diffusion and passivation by oxidation, making it possible to substantially improve the wear and corrosion resistance of parts made of ferrous metals, while guaranteeing a high degree of reproducibility , therefore a minimum dispersion.
- the invention covers any composition containing other alkali metal salts than sodium, taken alone or in mixtures, and the percentages of which are converted into sodium salts are those indicated above.
- concentrations will be expressed in% by weight corresponding to the sodium salts and designated by the expression “sodium unit”, which will serve to "normalize” the different mixtures, regardless of the associated metal cation (for example Na + , K + , Li + ).
- the temperature of the bath is between 350 and 550 ° C. and preferably between 450 and 530 ° C., and the duration of immersion of the parts in the bath is greater than 10 minutes.
- composition according to the invention is, from a qualitative point of view, of the same type as that cited in the patent FR 2 525 637 previously mentioned. In quantitative terms, however, it stands out in a very significant way. This can be explained as follows.
- the improvement in the wear resistance is due to the nitrided layer essentially while the improvement in the corrosion resistance depends on both the nitrided layer and the oxidized layer: both providing anodic protection.
- the effectiveness of this protection depends directly on the integrity of the barrier layer: it is sought to have an oxidized, continuous and waterproof surface layer.
- the nature of the layer forming in the oxidizing bath is known and consists essentially of iron oxide type Fe 3 O 4 , which is perfectly inert. It was therefore not a question of doing better in terms of the nature of the layer but of finding a solution to guarantee its sealing.
- the oxidizing bath composition which is the subject of the present application differs from known baths by the fact that it combines a percentage of powerful oxidizing salt which is clearly lower than that cited in patent FR 2 525 637, in combination with nitrates and also different hydroxides.
- the cationic species of the bath are only defined by the nature of the corresponding metals, namely the alkali metals. It is indeed of little importance that one or more cations are present and in the case where at least two cations are present simultaneously, the relationships between them have only a slight influence.
- composition according to the invention makes it possible to reconcile all of the criteria listed above.
- thermochemical treatment prior to oxidation produces on the surface of the parts a layer mainly composed of nitrides and / or carbonitrides, with also free iron in a minority proportion essentially present at the level of the defects of the layer. previous. It is probably this free iron which is responsible for the poor resistance to corrosion of parts that are simply nitrided, or carbonitrided.
- Nitrates are, however, oxidizing agents of medium activity and if they are capable of oxidizing the free iron present in the layer, they would not however be powerful enough to destabilize the nitrides or carbonitrides.
- Too much oxidizing agent on the other hand would lead to a weakening of the layer by the effect of the residual stresses of which it is the seat with the appearance of cracks, corrosion and scaling, detrimental to its tribological properties.
- the presence of carbonates would go in the direction of a moderation of these oxidation reactions.
- the temperature of the bath below a certain threshold, fixed by the carbonate content of the bath, it does not make it possible to achieve sufficient fluidity of the molten salts, which on the practical level leads to significant consumption. of salts by removal with the charges of parts, as well as a significant decantation at the bottom of the crucible. Too high a temperature leads to premature degeneration of the bath, with a concomitant decrease in its effectiveness.
- the oxidation operation which is carried out according to reactions in heterogeneous liquid / solid phase, acts primarily and preferentially on the outer part of the nitrided, sulfonitrided or carbonitrided layer. It is therefore understandable that the morphology and the degree of porosity of this layer can have a significant influence on the intensity levels and on the kinetics of the reactions.
- Parts made of non-alloy steel with 0.38% carbon were used, which were first subjected to a sulfonitriding treatment according to the teachings of the patents FR 2 171 993 and FR 2 271 307, by immersion for 90 minutes in a salt bath containing by weight 37% of cyanate ions and 17% of carbonate ions, the rest being alkaline cations K + , Na + and Li + , with in addition 10 to 15 ppm of S 2- ions.
- the temperature of the molten salts was 570 ° C.
- Friction tests the test pieces in this case were rings with a diameter of 35 mm and parallelepipedic plates with dimensions 30 x 18 x 8 mm. The friction test is carried out dry, pressing the ring against the large face of the plate, with a regularly increasing load from the initial value of 10 daN and with a sliding speed of 0.55 m / s. The results obtained are summarized in the following table:
- Example 1 The other operating conditions, as regards the prior nitriding, the duration of immersion of the parts in the oxidizing bath, and the final washing / drying operations, were the same as in Example 1.
- results obtained were qualified according to two reproducibility criteria, taking into account one of the color of the parts, the other of their resistance to corrosion in standardized salt spray.
- the color it can go from dark black (which is the optimum sought, for reasons of presentation of the treated parts), to reddish brown (which one seeks to avoid).
- Example 2 The procedure was as in Example 1, but varying from 0 to 1% the content of the oxidizing bath in Cr 2 O 7 2- anions.
- the introduction into the dichromate bath makes it possible to find a regular black color of the parts and there is concomitantly an increase in the corrosion potential above 1000 mV / DHW.
- the effect begins with 0.05% Cr 2 O 7 2- anion in the bath.
- the optimal influence is obtained with 0.2% Cr 2 O 7 2- ; beyond 0.2%, no further improvement is observed up to 0.5%; more than 0.5% of Cr 2 O 7 2- leads to a weakening of the layer which tends to flake.
- Example 2 As in Example 2, the results obtained were qualified, on the one hand by the color regularity of the treated parts, on the other hand by their resistance to corrosion with standardized salt spray:
- the carbonate content of the bath increases. This is due to the fact that when leaving the preliminary nitriding bath, the parts carry with them salts of said bath, which are composed essentially of carbonates and alkaline cyanates. These in turn transform into carbonates by reaction with the oxidizing salts.
- thermochemical diffusion is carried out by ionic or gas route it is the same, except that the conduct of the oxidizing bath is modified compared to what was described in Example 5: in this case in fact it there is no longer the entrainment of the nitriding salts; the carbonation of the oxidizing bath, as well as its drop in level, are slower.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Treatment Of Metals (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Powder Metallurgy (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
- Coating With Molten Metal (AREA)
- Luminescent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Electroplating Methods And Accessories (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9309814A FR2708941B1 (fr) | 1993-08-10 | 1993-08-10 | Procédé pour améliorer la résistance à l'usure et à la corrosion de pièces en métaux ferreux. |
FR9309814 | 1993-08-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0638661A1 EP0638661A1 (fr) | 1995-02-15 |
EP0638661B1 true EP0638661B1 (fr) | 1997-01-22 |
Family
ID=9450082
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP94401716A Expired - Lifetime EP0638661B1 (fr) | 1993-08-10 | 1994-07-26 | Procédé pour améliorer la résistance à l'usure et à la corrosion de pièces en métaux ferreux |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0638661B1 (zh) |
JP (1) | JP3083453B2 (zh) |
KR (1) | KR100273924B1 (zh) |
CN (1) | CN1054891C (zh) |
AT (1) | ATE148178T1 (zh) |
BR (1) | BR9403101A (zh) |
CA (1) | CA2129162C (zh) |
DE (1) | DE69401551T2 (zh) |
ES (1) | ES2097012T3 (zh) |
FR (1) | FR2708941B1 (zh) |
MY (1) | MY111901A (zh) |
PL (1) | PL177228B1 (zh) |
TW (1) | TW259815B (zh) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2731232B1 (fr) * | 1995-03-01 | 1997-05-16 | Stephanois Rech | Procede de traitement de surfaces ferreuses soumises a des sollicitations elevees de frottement |
JP4487340B2 (ja) | 1999-07-21 | 2010-06-23 | 日本精工株式会社 | 転がり軸受用保持器の製造方法 |
TW557330B (en) | 2000-11-29 | 2003-10-11 | Parker Netsushori Kogyo Kk | Improved salt bath nitrogenating method for corrosion-resistant iron material and iron units |
DE10124933A1 (de) * | 2001-05-21 | 2002-11-28 | Endress & Hauser Gmbh & Co Kg | Anordnung aus einem metallischen Deckel und einem metallischem Gehäuse eines Meßgerätes und Verfahren zu deren Herstellung |
EP2757423B1 (fr) * | 2013-01-17 | 2018-07-11 | Omega SA | Pièce pour mouvement d'horlogerie |
CN103451595B (zh) * | 2013-09-02 | 2015-09-23 | 中国科学院金属研究所 | 镁合金表面熔盐氧碳硫共渗耐腐蚀陶瓷涂层及制备和应用 |
CN113897579A (zh) * | 2021-09-30 | 2022-01-07 | 成都工具研究所有限公司 | 一种316l不锈钢工件低温qpq处理工艺 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2639244A (en) * | 1950-07-15 | 1953-05-19 | Remington Arms Co Inc | Metal finishing method |
DE2934113C2 (de) * | 1979-08-23 | 1985-05-09 | Degussa Ag, 6000 Frankfurt | Verfahren zur Erhöhung der Korrosionsbeständigkeit nitrierter Bauteile aus Eisenwerkstoffen |
FR2525637B1 (fr) * | 1982-04-23 | 1986-05-09 | Stephanois Rech Mec | Procede de traitement de pieces en metal ferreux en bain de sels oxydant, pour ameliorer leur resistance a la corrosion, les pieces contenant du soufre |
JPH0234793A (ja) * | 1988-07-26 | 1990-02-05 | Kobe Steel Ltd | スケール密着性の優れた加工用高強度熱延鋼板の製造方法 |
FR2672059B1 (fr) * | 1991-01-30 | 1995-04-28 | Stephanois Rech Mec | Procede pour conferer a des pieces en metal ferreux, nitrurees puis oxydees, une excellente resistance a la corrosion tout en conservant les proprietes acquises de friction. |
-
1993
- 1993-08-10 FR FR9309814A patent/FR2708941B1/fr not_active Expired - Lifetime
-
1994
- 1994-07-15 TW TW083106467A patent/TW259815B/zh not_active IP Right Cessation
- 1994-07-26 EP EP94401716A patent/EP0638661B1/fr not_active Expired - Lifetime
- 1994-07-26 AT AT94401716T patent/ATE148178T1/de active
- 1994-07-26 DE DE69401551T patent/DE69401551T2/de not_active Expired - Lifetime
- 1994-07-26 ES ES94401716T patent/ES2097012T3/es not_active Expired - Lifetime
- 1994-07-29 CA CA002129162A patent/CA2129162C/fr not_active Expired - Lifetime
- 1994-07-29 BR BR9403101A patent/BR9403101A/pt not_active IP Right Cessation
- 1994-08-08 PL PL94304595A patent/PL177228B1/pl unknown
- 1994-08-09 CN CN94109024A patent/CN1054891C/zh not_active Expired - Lifetime
- 1994-08-09 JP JP06187243A patent/JP3083453B2/ja not_active Expired - Lifetime
- 1994-08-10 MY MYPI94002091A patent/MY111901A/en unknown
- 1994-08-10 KR KR1019940019722A patent/KR100273924B1/ko active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
TW259815B (zh) | 1995-10-11 |
CN1101684A (zh) | 1995-04-19 |
PL177228B1 (pl) | 1999-10-29 |
FR2708941B1 (fr) | 1995-10-27 |
ATE148178T1 (de) | 1997-02-15 |
KR950006020A (ko) | 1995-03-20 |
FR2708941A1 (fr) | 1995-02-17 |
PL304595A1 (en) | 1995-02-20 |
JPH0776766A (ja) | 1995-03-20 |
KR100273924B1 (ko) | 2000-12-15 |
CA2129162A1 (fr) | 1995-02-11 |
ES2097012T3 (es) | 1997-03-16 |
DE69401551D1 (de) | 1997-03-06 |
DE69401551T2 (de) | 1997-07-03 |
MY111901A (en) | 2001-02-28 |
CN1054891C (zh) | 2000-07-26 |
BR9403101A (pt) | 1995-04-11 |
CA2129162C (fr) | 2000-12-12 |
JP3083453B2 (ja) | 2000-09-04 |
EP0638661A1 (fr) | 1995-02-15 |
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