EP1743955B1 - Pièce en acier avec une excellente résistance à la corrosion et une excellente résistance à la fatigue de corrosion et procédé de traitement de surface pour en obtenir - Google Patents
Pièce en acier avec une excellente résistance à la corrosion et une excellente résistance à la fatigue de corrosion et procédé de traitement de surface pour en obtenir Download PDFInfo
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- EP1743955B1 EP1743955B1 EP06014476A EP06014476A EP1743955B1 EP 1743955 B1 EP1743955 B1 EP 1743955B1 EP 06014476 A EP06014476 A EP 06014476A EP 06014476 A EP06014476 A EP 06014476A EP 1743955 B1 EP1743955 B1 EP 1743955B1
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- steel product
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- ratio
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- 229910000831 Steel Inorganic materials 0.000 title claims description 127
- 239000010959 steel Substances 0.000 title claims description 127
- 230000007797 corrosion Effects 0.000 title claims description 87
- 238000005260 corrosion Methods 0.000 title claims description 87
- 238000004381 surface treatment Methods 0.000 title claims description 39
- 238000000034 method Methods 0.000 title claims description 33
- 125000004429 atom Chemical group 0.000 claims description 53
- 239000011248 coating agent Substances 0.000 claims description 46
- 238000000576 coating method Methods 0.000 claims description 46
- 239000000243 solution Substances 0.000 claims description 37
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 34
- 238000001035 drying Methods 0.000 claims description 31
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims description 27
- 229910019142 PO4 Inorganic materials 0.000 claims description 20
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 19
- 239000007864 aqueous solution Substances 0.000 claims description 16
- 229910052804 chromium Inorganic materials 0.000 claims description 15
- 229910052782 aluminium Inorganic materials 0.000 claims description 14
- 229910052742 iron Inorganic materials 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 13
- 229910052748 manganese Inorganic materials 0.000 claims description 13
- 229910052710 silicon Inorganic materials 0.000 claims description 13
- 229910052698 phosphorus Inorganic materials 0.000 claims description 12
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 10
- 125000004437 phosphorous atom Chemical group 0.000 claims description 10
- 229940001007 aluminium phosphate Drugs 0.000 claims description 8
- 238000011282 treatment Methods 0.000 description 44
- 230000000052 comparative effect Effects 0.000 description 26
- 238000007654 immersion Methods 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000000463 material Substances 0.000 description 11
- 230000007423 decrease Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 238000009713 electroplating Methods 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- -1 aluminium ions Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005524 ceramic coating Methods 0.000 description 2
- 238000007739 conversion coating Methods 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 2
- 230000003628 erosive effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000002203 pretreatment Methods 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229910018125 Al-Si Inorganic materials 0.000 description 1
- 229910018520 Al—Si Inorganic materials 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 241000221535 Pucciniales Species 0.000 description 1
- 229910000639 Spring steel Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000009411 base construction Methods 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- STZCRXQWRGQSJD-UHFFFAOYSA-M sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonate Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- 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
- C23C22/05—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 aqueous solutions
- C23C22/06—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 aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—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 aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
- C23C22/20—Orthophosphates containing aluminium cations
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
Definitions
- the present invention relates to a steel product excellent in corrosion resistance and corrosion fatigue resistance, and a surface treatment method therefor.
- compositions of steel products are adjusted or coating films are formed by a surface treatment or the like in steel products used under corrosive environments.
- the purpose thereof is to prevent deterioration of static strength and fatigue strength characteristics due to corrosive thinning and occurrence of corrosion pits of the steel product from decreasing, and to prevent the appearance from worsening due to generation of rusts.
- a coating film treatment with a zinc-containing phosphate system may be applied relatively easily.
- corrosion resistance of the coating film is insufficient.
- steel products plated with a Zn-Al-Si base molten alloy (trade name Galvanium Steel, manufactured by Nittetsu Steel Sheet Corporation) have been known as backside-treated steel products having both a sacrificial corrosion protective action of Zn and a self-repair action of Al.
- this molten alloy plating requires a plating bath temperature of 400°C or more. For this reason, the method cannot be employed when a decrease of the mechanical strength caused by heating the steel product during immersion in a molten alloy is of problem.
- GB 1 451 145 A discloses a method for forming a corrosion-resistant coating consisting substantially of aluminium phosphate formed on a metal surface.
- the method comprises applying to the surface an aqueous acidic composition which has a pH of from 1.5 to 3.5 and which comprises phosphate ions and aluminium ions.
- EP 0 302 465 A2 describes a method for ceramic coating of steel products comprising coating the steel product by a chemical conversion treatment or an electrolytic treatment with an aluminium phosphate coating and applying a ceramic coating to the aluminium phosphate coated metal product.
- the chemical conversion treatment of the electrolytic treatment is conducted in an aqueous phosphoric acid mixture containing from 1.0 to about 10g/l aluminium ions and from about 1.0 to about 100g/l phosphate ions at a pH of from about 1.5 to 5.0.
- Patent document 1 discloses an organic-coated steel sheet excellent in corrosion resistance.
- the organic-coated steel sheet is produced by forming a chemical conversion coating film on a zinc-plated steel sheet followed by forming an organic coating film containing aluminium phosphate.
- the process of the steel sheet disclosed in patent document 1 is complex with high processing cost since the chemical conversion treatment should be applied before forming the organic coating film containing aluminium phosphate.
- Patent document 2 discloses a low iron loss unidirectional electromagnetic steel sheet and a method of producing the same.
- the electromagnetic steel sheet has a coating film comprising a first layer having a Young's modulus of 100 GPa or more and a difference of a linear coefficient of expansion of 2 X 10 -6 or more from that of the steel sheet, and a second layer containing aluminium phosphate.
- the steel sheet is baked at a temperature in the range of 400 to 1000°C after applying a coating liquid and drying the coating film for forming the second layer.
- it has been a problem in patent document 2 that the mechanical strength of the steel product decreases when the steel product is baked at a temperature in the range of 400 to 1000°C.
- an object of the present invention is to provide a steel product excellent in corrosion resistance and corrosion fatigue resistance and a surface treatment method therefore, wherein problems of high production cost, complex production process, hydrogen embrittlement and reduced strength of materials can be solved as a surface treatment method capable of substituting conventional surface treatment methods such as electroplating, chemical conversion coating and molten alloy plating.
- a steel product excellent in corrosion resistance and corrosion fatigue resistance comprising a coating film on the surface of the steel product, wherein a ratio of the number of Al atoms to the total number of Fe, C, A1, P and O atoms and optionally added Si, Mn and Cr atoms is 0.5% or more in an average composition of the coating film, and the number of Al atoms in the average composition of the coating film is higher than the number of Al atoms in an average composition of the steel product before surface treatment obtained by the process consisting of the steps of allowing an aqueous solution of H 3 PO 4 and Al (H 2 PO 4 ) 3 at room temperature for a 1000 seconds or more or at a temperature from 40 to 50°C for 30 seconds or more or at 30°C for 180 seconds or more having an acidity ratio in the range of 3.3 to 5.7 and containing AlPO 4 to contact the surface of the steel product to form a coating film, rinsing the steel product and drying the steel product after r
- the ratio of the number of Al atoms to the total number of Fe, C, Al, P and O atoms and optionally added Si, Mn and Cr atoms is 0.5% or more in an average composition in a region from the surface to a depth of 5 ⁇ m of the steel product.
- the ratio of the number of Al atoms to the total number of Fe, C, Al, P and O atoms and optionally added Si, Mn and Cr atoms is 3% or more.
- a surface treatment method for a steel product comprising allowing an aqueous solution of H 3 PO 4 and Al(H 2 PO 4 ) 3 at room temperature for a 1000 seconds or more at a temperature from 40 to 50°C for 30 seconds or more or at 30°C for 180°C or more having an acidity ratio in the range of 3.3 to 5.7 and containing AlPO 4 to contact the surface of the steel product; rinsing the steel product and drying the steel product after rinsing it or drying the steel product, rinsing the dried steel product and drying the rinsed steel product again.
- the method includes the step of drying at 50°C or less after allowing the steel product to contact the aqueous solution of H 3 PO 4 and Al(H 2 PO 4 ) 3 containing AlPO 4 and before rinsing.
- the acidity ratio of the aqueous solution of H 3 PO 4 and Al(H 2 PO 4 ) 3 containing AlPO 4 is in the range of 3.8 to 5.4.
- the aqueous solution of H 3 PO 4 and Al(H 2 PO 4 ) 3 having a concentration by weight of aluminium phosphate, AlPO 4 , in the range of 1-10%, and having an acidity ratio in the range of 3.8 to 5.4 as used as a surface treatment solution.
- the present inventors have completed the following invention through intensive studies on a mechanism of corrosion of a steel product and a chemical conversion treatment method.
- the acidity ratio is determined to be in the range of 3.3 to 5.7 in the methods cited in the items 3 and 4 of the invention for the following reasons. That is, the coating film is suppressed from being formed due to too severe corrosion of the steel product when the acidity ratio is less than 3.3. On the other hand, the formation of the coating film takes a long period of time since the corroding action of the steel product is too weak when the acidity ratio exceeds 5.7.
- the acidity ratio is more preferably in the range of 3.8 to 5.4.
- aqueous solution containing Al ions it is preferable in the methods cited in the items 3 and 4 of the invention to allow the aqueous solution containing Al ions to contact the surface of the steel product for 30 seconds or more at a temperature in the range of 40 to 50°C.
- the contact period is less than 30 seconds, the corroding action of the steel product is insufficient to fail in obtaining a coating film excellent in corrosion resistance and corrosion fatigue resistance.
- the contact period is less than 180 seconds, the corroding action of the steel product is insufficient to fail in obtaining a coating film excellent in corrosion resistance and corrosion fatigue resistance.
- the drying temperature is prescribed to be 50°C or less because, when the temperature exceeds 50°C, denseness of the coating film decreases due to too rapid evaporation of water to result in a decrease of the strength of the coating film.
- the treatment work is easy with a low processing cost in the steel product subjected to surface treatment in the invention, and excellent corrosion resistance and corrosion fatigue resistance are manifested without causing hydrogen embrittlement and decreased strength of the material.
- FIG. 1A shows an example of the surface treatment according to the invention, which is a first example of the surface treatment in which a drying step 2 as a post treatment is carried out after a rinsing step 1.
- FIG. 1B shows another example of the surface treatment according to the invention, which is a second example of the surface treatment in which the rinsing step 1 and a second drying step 2b as post treatments are sequentially carried out after a first drying step 2a.
- the surface of the steel product is preferably washed with an aqueous cleaning solution containing an organic solvent or a surfactant in advance for degreasing as in the pre-treatments in FIGS. 1A and 1B , or subjected to descaling with an acid solution.
- aqueous cleaning solution containing an organic solvent or a surfactant in advance for degreasing as in the pre-treatments in FIGS. 1A and 1B , or subjected to descaling with an acid solution.
- Water to be used for rinsing in FIGS. 1A and 1B desirably contains C1 as small as possible.
- the solution for use in the treatment in FIGS. 1A and 1B (referred to the treatment solution hereinafter) is obtained by adding aluminum phosphate (AlPO 4 ) in water, and further adding phosphoric acid (H 3 PO 4 ) for dissolving AlPO 4 .
- the concentration by weight of AlPO 4 is favorably in the range of 1 to 10%.
- the concentration of AlPO 4 exceeds 10%, the steel product may be eroded with the acid because the concentration of H 3 PO 4 added for dissolving AlPO 4 increases.
- concentration of AlPO 4 is below 1%, processability decreases since AlPO 4 is frequently replenished.
- industrial water, city water and distilled water may be used as water used for the solvent.
- Cl is preferably removed as much as possible.
- any methods such as immersion, air spray and brush coating may be used for allowing the treatment solution to contact the steel product. While the mechanism for forming the coating film has not been fully elucidated, it is conjectured as follows.
- Aluminum primary phosphate (Al(H 2 PO 4 ) 3 ), H 3 PO 4 and AlPO 4 are in an equilibrium state represented by the following formula (1) in the treatment solution.
- H 3 PO 4 interacts with Fe as shown in the following formula (2), and the concentration of H 3 PO 4 decreases in the solution near the surface of the steel product as shown in the formula (1). Accordingly, the equilibrium shown in the formula (1) shifts to the right side, and hardly soluble AlPO 4 seems to precipitate on the surface of the steel product to form a coating film.
- the coating film is considered to be formed based on the steel product corroding action of H 3 PO 4 and deposition of hardly soluble AlPO 4 formed by decomposition of Al(H 2 PO 4 ) 3 . It may be also considered that dissolved Fe is contained in AlPO 4 formed as described above, and a film comprising Al, Fe, P and O is formed. Accordingly, the molar ratio between H 3 PO 4 and Al(H 2 PO 4 ) 3 is important in the treatment condition by the treatment solution of the invention, and specifically, control of the acidity ratio is important.
- the term "acidity ratio" as used herein refers to a ratio of a point of acidity of total phosphoric acid (H 3 PO 4 and Al(H 2 PO 4 ) 3 ) to a point of acidity of free phosphoric acid (H 3 PO 4 ) in the treatment solution.
- the "point” is as described below.
- a treatment solution (10 cc) is neutralized with 0.1 N sodium hydroxide (NaOH) by adding 2 to 3 drops of methyl orange solution as an indicator at room temperature.
- the point of acidity of free phosphoric acid is the volume of the aqueous NaOH solution represented by a cc unit when the color of the solution changes to orange.
- the point of total acidity is the volume of the aqueous NaOH solution represented by the cc unit when the same solution is neutralized as described above by adding 2 to 3 drops of phenolphthalein solution and the color of the solution changes to pale pink.
- the acidity ratio of the treatment solution can be controlled by adding a basic aqueous solution such as an aqueous NaOH solution.
- a treatment solution ready for forming the coating film may be obtained for maintaining the equilibrium in formula (1) by increasing the acidity ratio, or by decreasing the amount of H 3 PO 4 .
- the acidity ratio is in the range of 3.3 to 5.7, particularly of 3.8 to 5.4.
- the acidity ratio is less than 3.3 (too much H 3 PO 4 )
- the coating film is suppressed from being formed due to too vigorous corrosion of the steel product.
- the acidity ratio exceeds 5.7 (to little H 3 PO 4 )
- a long period of time is necessary for forming the coating film since the corrosion action for the steel product is weak.
- the required contact periods of the steel product with the treatment solution are 1000 seconds or more, 180 seconds or more and 30 seconds or more when the temperatures of the treatment solution are room temperature, 30°C and in the range of 40 to 50°C, respectively.
- the upper limit temperature of the treatment solution is desirably 50°C or less since temperature control is difficult at a higher temperature while the cost for maintaining the temperature is high.
- the steel product may be immediately rinsed (first example of surface treatment: A) after the above-mentioned treatment as shown in FIG. 1A , or may be rinsed after drying (second example of surface treatment: B) after the above-mentioned treatment as shown in FIG. 1B . Since drying is applied for removing adhered water, the steel product may be left at room temperature or in a heated atmosphere. Otherwise, a conventional drying furnace may be used.
- the temperature of the first drying step in the second example of the surface treatment is desirably 50°C or less. A temperature exceeding 50°C is not preferable since water is so rapidly evaporated that denseness of the coating film decreases to reduce the strength of the coating film.
- the steel product treated as described above is expected to have a sacrificial corrosion protective action by the Al component in the coating film formed on the surface and an action for forming a passive film by oxidation of the Al component.
- the concentration of Al atoms in the coating film at the surface of the steel product is quantitatively analyzed by elementary analysis in the region from the surface to a depth of 5 ⁇ m using an EDX (Energy Dispersive X-ray spectroscopy) device, and is corrected by ZAF correction (Z: difference of emitted X-ray intensity depending on difference of sample compositions; A: absorption X-ray in sample; F: fluorescence excitation by emitted X-rays in sample).
- the ratio of A (the ratio of the number of Al atoms) to B should be 0.5% or more, particularly desirably 3% or more.
- the ratio of the number of Al atoms is less than 0.5%, both the above-mentioned sacrificial corrosion protective action and action for forming a passive film are so weak that sufficient corrosion resistance and corrosion fatigue resistance cannot be obtained.
- a surface treatment with a low cost is possible since aluminum phosphate, phosphoric acid and distilled water are cheaply and readily available and the treatment is simple. Since the treatment solution is weakly acidic and the amount of hydrogen generated from the steel product is very small, the steel product is substantially free from hydrogen embrittlement. Further, all the treatments are performed at 50°C or less, so that the strength of the materials is hardly reduced.
- the surface of a steel product SAE9254 (Fe-0.56%C-1.42%Si-0.75%Mn-0.68% Cr) with a diameter of 4 mm and a length of 20 to 80 mm was treated under the conditions shown in Table 1.
- the steel product was a material obtained by removing in advance solid and thick oxidized scales by blast treatment.
- the pre-treatment procedure comprises washing the steel product with distilled water, degreasing with acetone, and then removing the scale again by immersing the steel product in dilute aqueous hydrochloric acid.
- the steel product to be treated was immersed in the treatment solution under the conditions shown in Table 1, washed with distilled water, and allowed to spontaneously dry (the condition in which the column of drying at 50°C in Table 1 is represented by "none (-)").
- the acidity ratio was controlled by adding an aqueous sodium hydroxide solution in the treatment solution.
- the steel product was dried after immersion, if necessary, by leaving it in an oven maintained at 50°C in air (the condition in which the column of drying at 50°C in Table 1 is represented by "yes").
- the ratio of the number of Al atoms on the surface of the steel product, corrosion resistance and corrosion fatigue resistance were evaluated by using the surface-treated product as a test material.
- the ratio of the number of Al atoms in the region from the surface to a depth of 5 ⁇ m was quantitatively analyzed through elementary analysis by using the EXD device, and the measured value was corrected by ZAF.
- the ratio of A to B was calculated and evaluated based on the result of the quantitative analysis, where A denotes the number of Al atoms and B denotes the total number of Fe, C, Al, P and O atoms, and of Si, Mn, Cr atoms that are optionally added.
- the material with a ratio of 3% or more was represented by "3 or more"
- the product with a ratio in the range of 0.5% or more and less than 3% was represented by "0.5 to 3”
- the product with a ratio of less than 0.5% was represented by "less than 0.5".
- the corrosion resistance was evaluated by leaving the test material in a constant temperature-constant humidity chamber (26°C, 95% RH) for 200 hours. The proportion of the rusted area to the total area after leaving for 200 hours was visually evaluated.
- the products with a surface ratio of the rusted surface of less than 80%, in the range of 80% or more and less than 90%, and 90% or more were evaluated as "best (a level having quite excellent corrosion resistance)", “good (a level having excellent corrosion resistance)” and “poor (a level having poor corrosion resistance)", respectively, by using the proportion of the rusted area C in Comparative Example 1 as a standard.
- the corrosion fatigue resistance was evaluated by repeating the steps of vibrating a test material left under salt water spray (35°C, 5% NaCl) for 30 minutes at a shear stress ⁇ of 733 ⁇ 441 MPa for 3,000 times (1.5 Hz, for about 33 minutes), and leaving the test material in a constant temperature-constant humidity chamber (26°C, 95% RH) until the test material was broken.
- the corrosion fatigue resistance was evaluated as “best (a level quite excellent in corrosion fatigue resistance)" when the duration count was 120% or more, as “good (a level excellent in corrosion fatigue resistance)” when the duration count was in the range of 10% or more and less than 120%, and as “poor (a level poor in corrosion fatigue resistance” when the duration count was less than 110% on the basis of the duration count D in Comparative Example 1 as a standard.
- the results are shown in Table 1.
- the steel product in Comparative Example 1 is a non-treated product, and serves as a standard for evaluating corrosion resistance and corrosion fatigue resistance.
- Table 1 Surface treatment condition Evaluation of ratio of Al atoms Evaluation of corrosion resistance Evaluation of corrosion fatigue resistance Surface treatment example Acidity ratio Bath temperature (°C) Immersion period (seconds) Temperature of drying step (°C) Comparative example 1 - - - - - Less than 0.5 Poor Poor Comparative example 2 B 2.0 Room temperature 180 50 Less than 0.5 Poor Poor Comparative example 3 B 2.5 Room temperature 180 50 Less than 0.5 Poor Poor Example 1 B 3.3 Room temperature 180 50 0.5 to 3 Good Good Example 2 B 3.8 Room temperature 180 50 3 or more Best Best Example 3 B 4.7 Room temperature 180 50 3 or more Best Best Example 4 B 5.0 Room temperature 180 50 3 or more Best Best Example 5 B 5.4 Room temperature 180 50 3 or more Best Best Example 6 B 5.7 Room temperature 180 50 0.5 to 3 Good Good Example 7 B 4.7 Room temperature 5 50 0.5 to 3 Good Good Example 8 B 4.7
- Steel products in Comparative Examples 2 and 3 and in Examples 1 to 6 are in accordance with the second examples of the surface treatment in FIG. 1B . That is, the products were dried in air by heating at 50°C (first drying step) after immersing in the treatment solution at room temperature for 180 seconds, and then spontaneously dried again (second drying step) after rinsing, where the acidity ratio of the treatment solution was changed in the range of 2.0 to 5.7.
- the ratio of the number of Al atoms is "0.5 to 3" or "3 or more" in the products in Examples 1 to 6 in which the acidity ratio is in the range of 3.3 to 5.7.
- Corrosion resistance and corrosion fatigue resistance are "good (excellent level)” or “best (quite excellent level)” in the products in Examples 1 to 6 in which the acidity ratio is in the range of 3.3 to 5.7.
- both the corrosion resistance and corrosion fatigue resistance are “best (quite excellent level)” in the products in Examples 2 to 5 in which the acidity ratio is in the range of 3.8 to 5.4.
- both the corrosion resistance and corrosion fatigue resistance are “poor (poor level)” in the products in Comparable Examples 2 and 3 in which the activity ratio is 2.5 or less.
- the steel products in Examples 7 to 10 are in accordance with the second example of the surface treatment in FIG. 1B . That is, the products were dried by heating at 50°C in air after immersing in the treatment solution with an acidity ratio of 4.7 at room temperature, and then spontaneously dried after rinsing, where the immersion period was changed in the range form 5 to 1000 seconds.
- the atomic ratio of the number of Al atoms is "0.5 to 3" or "3 or more” in all these examples. In particular, the ratio of the number of Al atoms is "3 or more" in the products in all Examples 8 to 10 in which the immersion period is 30 seconds or more.
- Corrosion resistance and corrosion fatigue resistance are "good (excellent level)” or “best (quite excellent level)” in the products in all the examples. In particular, corrosion resistance and corrosion fatigue resistance are "best (quite excellent level)" in the products in Examples 9 and 10 in which the immersion period is 360 seconds or more.
- the steel products in Comparative Examples 4 to 7 and Example 11 are in accordance with the first example of the surface treatment in FIG. 1A . That is, the products were rinsed and spontaneously dried after immersing in the treatment solution with an acidity ratio of 4.7 at room temperature, where the immersion period was changed in the range of 5 to 1000 seconds.
- the atomic ratio of the number of Al atoms is "3 or more" in the product in Example 11 with an immersion period of 1000 seconds. However, the ratio of the number of Al atoms is "less than 0.5" in the products in Comparative Examples 4 to 7 with an immersion period of 360 seconds or more.
- Corrosion resistance and corrosion fatigue resistance are "best (quite excellent level)" in the product in Example 11 with an immersion period of 1000 seconds. However, corrosion resistance and corrosion fatigue resistance are "poor” (poor level) in the products in Comparative Examples 4 to 7 with an immersion period of 360 seconds or less.
- the steel products in Comparative Examples 8 and 9 and Examples 12 to 14 are in accordance with the first example of the surface treatment in FIG. 1A . That is, the products were rinsed and spontaneously dried after immersing in the treatment solution with an acidity ratio of 4.7 at 30°C, where the immersion period was changed in the range form 5 to 1000 seconds.
- the atomic ratio of the number of A1 atoms is "0.5 to 3" or "3 or more" in the products in Examples 12 to 14 with an immersion period of 180 seconds or more.
- the ratio of the number of Al atoms in the product in Example 14 with an immersion period of 1000 seconds is "3 or more".
- the ratio of the number of Al atoms is "less than 0.5" in the products in Comparative examples 8 and 9 with an immersion period of 30 seconds or less.
- Corrosion resistance and corrosion fatigue resistance are "good (excellent level)” or “best (quite excellent level)” in the products in Examples 12 to 14 with an immersion period of 180 seconds or more.
- corrosion resistance and corrosion fatigue resistance are “best (quite excellent level)” in the product in Example 14 with an immersion period of 1000 seconds.
- Corrosion resistance and corrosion fatigue resistance are “poor (poor level)” in the products in Comparative Examples 8 and 9 with an immersion period of 30 seconds or less.
- the steel products in Comparative Examples 10 and 11 and Examples 15 to 22 are in accordance with the first example of the surface treatment in FIG. 1A . That is the products were rinsed and spontaneously dried after immersing in the treatment solution with an acidity ratio of 4.7 at 40°C or 50°C, where the immersion period was changed in the range of 5 to 1000 seconds.
- the ratio of the number of Al atoms is "3 or more" in the products in Examples 15 to 22 with an immersion period of 30 seconds or more. However, the ratio of the number of Al atoms is "less than 0.5" in the products in Comparative Examples 10 and 11 with an immersion period of 5 seconds.
- Corrosion resistance and corrosion fatigue resistance are "good (excellent level)” or “best (quite excellent level)” in the products in Examples 15 to 22 with an immersion period of 30 or more.
- corrosion resistance and corrosion fatigue resistance are “best (quite excellent level)” in the products in Examples 16 to 18 and Examples 20 to 22 with an immersion period of 180 seconds.
- corrosion resistance and corrosion fatigue resistance are "poor (poor level)” in the products in Comparative Examples 10 and 11 with an immersion period of 5 seconds.
- the invention is not restricted to a steel product SAE9254 having the above-mentioned diameter and length, instead the invention is applicable to other steel products at a practical stage in the range not departing from the spirit of the invention. Specifically, the invention is applicable to all the steel products containing at least Fe and C with optionally added at least one of Si, Mn and Cr.
- the surface treatment conditions for example, bath temperature, immersion period and the like
- the surface treatment conditions are not restricted to those as set forth in the examples, but an appropriate combination is possible in the range not modifying the spirit of the invention.
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Claims (7)
- Procédé de traitement de surface pour un produit en acier, caractérisé en ce que comprenant les étapes de :mise en contact d'une solution aqueuse de H3PO4 et Al(H2PO4)3 à la température ambiante pendant 1 000 secondes ou plus, ou à une température de 40 à 50°C pendant 30 secondes ou plus, ou à 30°C pendant 180 secondes ou plus, ayant un rapport d'acidité dans la plage de 3,3 à 5,7 et contenant AlPO4, avec la surface du produit en acier pour former un film de revêtement ;rinçage (1) du produit en acier et séchage (2) du produit en acier après rinçage (1) de celui-ci, ouséchage (2a) du produit en acier, rinçage (1) du produit en acier séché et séchage à nouveau (2b) du produit en acier rincé.
- Procédé de traitement de surface pour un produit en acier selon la revendication 1, caractérisé en ce qu'il comprend l'étape (2a) de séchage à 50°C ou moins après avoir laissé le produit en acier au contact de la solution aqueuse de H3PO4 et Al(H2PO4)3 contenant AlPO4 et avant rinçage.
- Procédé de traitement de surface pour un produit en acier selon l'une quelconque des revendications 1 ou 2, caractérisé en ce que le rapport d'acidité de la solution aqueuse de H3PO4 et Al(H2PO4)3 contenant AlPO4 est dans la plage de 3,8 à 5,4.
- Procédé de traitement de surface pour un produit en acier selon l'une quelconque des revendications 1 ou 2, caractérisé en ce qu'une solution aqueuse de H3PO4 et Al(H2PO4)3 ayant une concentration en poids de phosphate d'aluminium, AlPO4, dans la plage de 1 à 10%, et ayant un rapport d'acidité dans la plage de 3,8 à 5,4, est utilisée comme solution de traitement de surface.
- Produit en acier excellent en termes de résistance à la corrosion et de résistance à la fatigue à la corrosion, caractérisé en ce que comprenant un film de revêtement sur la surface du produit en acier, dans lequel un rapport du nombre d'atomes d'Al sur le nombre total d'atomes Fe, C, Al, P et O, et optionnellement d'atomes Si, Mn et Cr est 0,5% ou plus dans une composition moyenne du film de revêtement, et le nombre d'atomes d'Al dans la composition moyenne du film de revêtement est supérieur au nombre d'atomes d'Al dans une composition moyenne du produit en acier avant le traitement de surface, obtenu par le procédé consistant en les étapes de :mise en contact d'une solution aqueuse de H3PO4 et Al(H2PO4)3 à la température ambiante pendant 1 000 secondes ou plus, ou à une température de 40 à 50°C pendant 30 secondes ou plus, ou à 30°C pendant 180 secondes ou plus, ayant un rapport d'acidité dans la plage de 3,3 à 5,7 et contenant AlPO4, avec la surface du produit en acier pour former un film de revêtement ;rinçage (1) du produit en acier et séchage (2) du produit en acier après rinçage (1) de celui-ci, ouséchage (2a) du produit en acier, rinçage (1) du produit en acier séché et séchage à nouveau (2b) du produit en acier rincé.
- Produit en acier excellent en termes de résistance à la corrosion et de résistance à la fatigue à la corrosion selon la revendication 5, caractérisé en ce que le rapport du nombre d'atomes d'Al sur le nombre total d'atomes Fe, C, Al, P et 0 et optionnellement d'atomes Si, Mn et Cr est 0,5% ou plus dans une composition moyenne dans une région de la surface jusqu'à une profondeur de 5 µm du produit en acier.
- Produit en acier excellent en termes de résistance à la corrosion et de résistance à la fatigue à la corrosion selon la revendication 5 ou 6, caractérisé en ce que le rapport du nombre d'atomes d'Al sur le nombre total d'atomes Fe, C, Al, P et 0 et optionnellement d'atomes Si, Mn et Cr est 3% ou plus.
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Application Number | Priority Date | Filing Date | Title |
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JP2005206977A JP5153063B2 (ja) | 2005-07-15 | 2005-07-15 | 鋼材の表面処理方法 |
Publications (3)
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EP1743955A2 EP1743955A2 (fr) | 2007-01-17 |
EP1743955A3 EP1743955A3 (fr) | 2007-01-24 |
EP1743955B1 true EP1743955B1 (fr) | 2012-05-02 |
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EP06014476A Not-in-force EP1743955B1 (fr) | 2005-07-15 | 2006-07-12 | Pièce en acier avec une excellente résistance à la corrosion et une excellente résistance à la fatigue de corrosion et procédé de traitement de surface pour en obtenir |
Country Status (6)
Country | Link |
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US (1) | US20070012382A1 (fr) |
EP (1) | EP1743955B1 (fr) |
JP (1) | JP5153063B2 (fr) |
KR (1) | KR101285969B1 (fr) |
CN (1) | CN1924097B (fr) |
ES (1) | ES2387395T3 (fr) |
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CN101634022B (zh) * | 2008-07-24 | 2013-03-27 | 中国第一汽车股份有限公司 | 车载scr封装用铁素体不锈钢的耐腐蚀钝化处理工艺 |
CN111187965B (zh) * | 2019-12-31 | 2021-08-31 | 中南大学湘雅二医院 | 一种FeMn生物可降解合金及其制备方法 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
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GB1084017A (en) * | 1963-09-30 | 1967-09-20 | Jawata Iron & Steel Co Ltd | Pretreating process for phosphate-treating steel sheets or plated steel sheets |
JPS536945B2 (fr) * | 1973-02-27 | 1978-03-13 | ||
US3922396A (en) * | 1974-04-23 | 1975-11-25 | Chromalloy American Corp | Corrosion resistant coating system for ferrous metal articles having brazed joints |
IN158643B (fr) * | 1982-05-12 | 1986-12-27 | Westinghouse Electric Corp | |
DE3337794A1 (de) * | 1982-11-02 | 1984-05-03 | Metallgesellschaft Ag, 6000 Frankfurt | Verfahren zur vorbereitung von metalloberflaechen fuer die elektrotauchlackierung |
JPH0730459B2 (ja) * | 1987-08-03 | 1995-04-05 | 日本パ−カライジング株式会社 | 金属へのセラミックコ−ティング法 |
DE3800835A1 (de) * | 1988-01-14 | 1989-07-27 | Henkel Kgaa | Verfahren zur phosphatierung von metalloberflaechen |
CN1019822B (zh) * | 1989-09-28 | 1992-12-30 | 本钢建筑材料金属加工厂 | 在铜基体上涂、渗金属的方法 |
JPH04124282A (ja) * | 1990-09-14 | 1992-04-24 | Babcock Hitachi Kk | 方向性珪素鋼板への絶縁被膜の形成方法 |
JPH05230547A (ja) * | 1992-02-19 | 1993-09-07 | Kanai Hiroyuki | バネ用オイルテンパー線の製造方法 |
JPH06228721A (ja) * | 1992-12-02 | 1994-08-16 | Praxair St Technol Inc | 耐溶融金属侵食性シール材およびその製造方法 |
JP3324633B2 (ja) | 1996-04-09 | 2002-09-17 | 新日本製鐵株式会社 | 低鉄損一方向性電磁鋼板およびその製造方法 |
JP3381647B2 (ja) | 1998-11-20 | 2003-03-04 | 日本鋼管株式会社 | 耐食性に優れた有機被覆鋼板 |
US6465114B1 (en) * | 1999-05-24 | 2002-10-15 | Nippon Steel Corporation | -Zn coated steel material, ZN coated steel sheet and painted steel sheet excellent in corrosion resistance, and method of producing the same |
JP4234872B2 (ja) * | 2000-02-01 | 2009-03-04 | 新日本製鐵株式会社 | 樹脂密着性と樹脂積層後の耐食性に優れた樹脂被覆容器用表面処理鋼板の製造方法 |
JP2001335956A (ja) * | 2000-05-23 | 2001-12-07 | Nippon Steel Corp | Cr含有鋼製油井管継ぎ手のりん酸マンガン系化成処理方法 |
CN1236104C (zh) * | 2002-08-16 | 2006-01-11 | 中国科学院金属研究所 | 镁合金无铬化学转化膜成膜溶液 |
-
2005
- 2005-07-15 JP JP2005206977A patent/JP5153063B2/ja not_active Expired - Fee Related
-
2006
- 2006-07-11 US US11/484,988 patent/US20070012382A1/en not_active Abandoned
- 2006-07-12 ES ES06014476T patent/ES2387395T3/es active Active
- 2006-07-12 EP EP06014476A patent/EP1743955B1/fr not_active Not-in-force
- 2006-07-13 KR KR1020060065909A patent/KR101285969B1/ko not_active IP Right Cessation
- 2006-07-14 CN CN2006101059205A patent/CN1924097B/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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KR20070009446A (ko) | 2007-01-18 |
JP2007023337A (ja) | 2007-02-01 |
EP1743955A3 (fr) | 2007-01-24 |
US20070012382A1 (en) | 2007-01-18 |
JP5153063B2 (ja) | 2013-02-27 |
CN1924097B (zh) | 2011-02-23 |
CN1924097A (zh) | 2007-03-07 |
EP1743955A2 (fr) | 2007-01-17 |
KR101285969B1 (ko) | 2013-07-12 |
ES2387395T3 (es) | 2012-09-21 |
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