WO2005106074A1 - Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part - Google Patents

Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part Download PDF

Info

Publication number
WO2005106074A1
WO2005106074A1 PCT/EP2005/003911 EP2005003911W WO2005106074A1 WO 2005106074 A1 WO2005106074 A1 WO 2005106074A1 EP 2005003911 W EP2005003911 W EP 2005003911W WO 2005106074 A1 WO2005106074 A1 WO 2005106074A1
Authority
WO
WIPO (PCT)
Prior art keywords
equal
coating
iron
phosphates
crystalline layer
Prior art date
Application number
PCT/EP2005/003911
Other languages
French (fr)
Other versions
WO2005106074A8 (en
Inventor
Francisco Varela Losada
Original Assignee
Delphi Diesel Systems S.L.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Delphi Diesel Systems S.L. filed Critical Delphi Diesel Systems S.L.
Priority to EP05759114A priority Critical patent/EP1660699A1/en
Priority to US10/570,778 priority patent/US20080264523A1/en
Publication of WO2005106074A1 publication Critical patent/WO2005106074A1/en
Publication of WO2005106074A8 publication Critical patent/WO2005106074A8/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C22/00Chemical 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
    • C23C22/05Chemical 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
    • C23C22/06Chemical 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
    • C23C22/07Chemical 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
    • C23C22/08Orthophosphates
    • C23C22/18Orthophosphates containing manganese cations
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C22/00Chemical 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
    • C23C22/73Chemical 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 characterised by the process

Definitions

  • This invention relates to a method for applying a phosphate coating on a steel or iron part.
  • the invention also relates to a steel or iron part obtained by said method.
  • the invention aims to overcome this disadvantage.
  • This purpose is achieved by a method for applying a phosphate coating on an iron or steel part, characterised in that it comprises:
  • a first coating step comprising a first phosphating, through which on the base metal of said part a first crystalline layer of iron and manganese phosphates is obtained; - an intermediate step of partial pickling of said first crystalline layer of phosphates, leaving said base metal partially uncovered, and
  • a second coating step comprising a second phosphating through which, on said partially pickled first crystalline layer of phosphates and on said partially uncovered base metal, a second crystalline layer of iron and manganese phosphates is obtained.
  • a coating with a particularly small thickness is achieved, having a particularly fine crystallisation with a high density of crystals by surface unit in the part surface. This leads, on the one hand, to a coefficient of friction much lower than the one that can be obtained by the known coating methods and, on the other hand, to a higher adherence of the coating on the part surface.
  • a known coating method can be applied to carry out these first and second coating steps each one comprising a phosphating; in particular, said coating steps can comprise, typically, subsequent steps of treatment by immersing the part in a series of bathes, being these steps typically as follows : cleaning, degreasing, surface activating, phosphating, rinsing, drying and, optionally, greasing.
  • the special feature of the method according to the invention is, therefore, the fact of having introduced a partial pickling step applied to the crystalline layer of phosphates which has been obtained by means of a coating method that may be one of the already known, as it has been said, and after that carrying out a new phosphating on said pickled layer.
  • This intermediate pickling stage confers to the surface of the part a particular state that allows the second crystalline layer to be formed with better crystallographic features than the first one. Indeed, after the pickling the surface of the part has such a microstructure and activity that, when applying the second phosphating crystal, grains of phosphates are formed on the nucleation sites of said microstructure, growing with particularly reduced size and in an especially homogeneous form.
  • This advantageous features of the part surface after the intermediate pickling step are precisely due to the fact that said pickling is partial, that is to say that on said surface the rest of the first crystalline layer and the base metal coexist.
  • an iron or steel part with an iron and manganese phosphate coating characterised in that said coating has an homogeneous morphology with crystalline formations shaped as needles or columns of a size equal or lower than 2 ⁇ m, having said coating a thickness equal or less than 2 ⁇ m.
  • said coating has an apparent density higher or equal to 3 g/cm 3 and lower or equal to 10 g/cm 3 and, preferably, said coating has an specific weight higher or equal to 1.5 g/m 2 and lower or equal to 7 g/m 2 .
  • the specific weight of coating expressed in g/m 2 , refers to the total mass of the coating deposited by surface unit.
  • the apparent density of coating is defined as a ratio between the specific weight of the coating and the coating thickness.
  • said intermediate step of partial pickling consists in a mechanical pickling by erosion in an abrasive medium, by which it is obtained a surface finish suitable for growing the second layer of phosphates with the wished features of a lower grain size and a higher homogeneity.
  • mechanical pickling in an abrasive medium has the advantage of providing a partial pickling with a surface finish wherein the completely pickled surface of the base metal, that is, the surface completely free of phosphate crystals of the first layer, coexists with microcavities coated by phosphate crystals of the first layer which are firmly adhered to the metal substrate.
  • This state is particularly advantageous for the growth of the second layer of phosphates with the wished features.
  • said mechanical pickling by erosion in an abrasive medium lasts until at least 15% of the total surface of said first crystalline layer of phosphates had been completely pickled. In this way, a particularly fine and well adhered second layer of phosphates is obtained.
  • said mechanical pickling by erosion in an abrasive medium consists in a rotofinishing using ceramic abrasive with a continuous inflow of an aqueous solution comprising a surfactant and a chemical flocculation agent, having said aqueous solution a pH higher or equal to 6 and lower or equal to 10.
  • the intermediate step of pickling provides a surface finish suitable for the grain growth during the second phosphating.
  • said first and second phosphatings consist in an immersion of said part in an acid solution comprising at least phosphoric acid, metallic acid phosphates, manganese, nickel, iron 2+ and nitrates, having said acid solution a total acid value higher or equal to 58 and lower or equal to 100 and a ratio between total acid and free acid higher or equal to 5 and lower or equal to 7, and being the content of iron 2+ in said acid solution lower or equal to 2.5 g/l.
  • the free acid is defined as the concentration of hydrogen ions corresponding to the first constant of dissociation of phosphoric acid not replaced by metallic ions, being expressed as millilitres or points of solution of NaOH 0.1 N which are necessary in order to achieve the neutralisation of said free acid from a sample of 10 ml of bath.
  • total acid it is understood the millilitres or points of NaOH 0.1N which are necessary in order to achieve the neutralisation corresponding to the equivalence point of secondary phosphates, phosphoric acid and primary phosphates present in a sample of 10 ml of bath, being also this value influenced by the precipitation of different metallic cations present in the bath.
  • This method is able to advantageously generate a mixed crystalline phase of manganese and iron phosphates of hurealite type, which constitutes said first and second crystalline layers (although the second crystalline layer, as it has been said, has different crystallographic properties regarding the distribution and the grain size).
  • the immersion of said part in said acid solution is carried out by keeping said acid solution at a temperature higher or equal to 95°C and lower or equal to 98°C and it lasts while gas is released from the metallic surface of said part, whereby the formation of said step mixed crystalline phase is optimised and a well developed crystalline layer of phosphates is obtained.
  • the invention further refers to a steel or iron part with a coating obtained according to the method of the invention, having said part the particular features described above.
  • Fig 1a 10 minutes Fig 1 b: 20 minutes Fig 1c: 30 minutes Fig 1d: 40 minutes Fig 1e: 50 minutes Fig 1f: 60 minutes
  • Figs. 2a, 2b, 2c, 2d, 2e and 2f images of electronic microscope showing with a x5000 enlargement the morphology of the second crystalline layer after the second phosphating; the different images are surface views corresponding to the results obtained by rotofinishing durations in the intermediate step of partial pickling;
  • Fig. 2a 10 minutes Fig. 2b: 20 minutes Fig. 2c: 30 minutes Fig. 2d: 40 minutes Fig. 2e: 50 minutes Fig. 2f: 60 minutes;
  • Figs. 3a and 3b images of electronic microscope showing with a x5000 enlargement, in surface views, the morphology of the crystalline layer of phosphates;
  • Fig. 3a corresponds to the results obtained after the first phosphating, while
  • Fig. 3b corresponds to the results obtained after the second phosphating;
  • Figs. 4a and 4b images of electronic microscope similar to the ones of Figs. 3a and 3b, respectively, but in cross-sectional view; in this case, the image of Fig. 4a has a x ⁇ OOO enlargement and Fig. 4b has a x13000 enlargement;
  • Fig. 5 a comparative graphic of the thickness of the crystalline layer of phosphates, after the first phosphating and after the second phosphating; the total thickness of the coating e, expressed in ⁇ m, is represented in the axis of ordinates; the different points correspond to different measure points in the part surface; the points represented by a triangle correspond to the situation after the first phosphating, whereas the points represented by a filled circle correspond to the situation after the second phosphating;
  • Fig. 6a a comparative graphic of the roughness Rk of the part surface, after the first phosphating and after the second phosphating; the roughness Rk, expressed in ⁇ m, is represented in the axis of ordinates; the different points correspond to different measure points in the part surface; the points represented by a triangle correspond to the situation after the first phosphating, whereas the points represented by a filled circle correspond to the situation after the second phosphating.
  • the method according to the invention is applied, as a non-limiting example, on a soft mechanised steel part subjected to a thermal treatment consisting in quenching and tempering.
  • said part is a recess for a roller used in pumps for injecting gas-oil at very high pressures and the applied method comprise the following steps:
  • Second coating step comprising a second phosphating and being identical to the first coating step, obtaining on said first crystalline layer of phosphates partially pickled a second crystalline layer of iron and manganese phosphates.
  • the morphological features of the second crystalline layer of phosphates mainly depends on the time of mechanical pickling of the first crystalline layer of phosphates, that is, the percentage of surface which is completely pickled, as it can be seen in Figs. 1a-1f and 2a-2f. In the case of the part treated in this example, this percentage amounts to 60%. However, depending on the type of part to be treated and on the wished results, a lower or higher time for pickling can be applied in order to obtain a higher or lower percentage of completely pickled surface. It has been observed, nevertheless, that a particularly good result is obtained when this percentage is higher or equal to 15%, even though with a lower percentage satisfactory results, in any case higher than the ones of the methods of the prior art, can be obtained.
  • the first coating step corresponds per se to a method for obtaining a coating by phosphating according to the state of the prior art.
  • Figs. 3a, 3b, 4a, 4b, 5 and 6 show that the method according to the invention provides a coating of a much higher quality than the one that can be obtained by a method of the prior art, that is applying simply a first coating step.
  • Figs. 3a, 3b and 4a, 4b can be observed that the crystallographic features of the coating layer after the second phosphating are completely different from the ones observed after the first phosphating.
  • the coating layer obtained after the second coating step has a remarkably lower thickness and a much lower roughness than the layer obtained after the first coating step.
  • the decrease of the crystal size as well as its higher density imply a higher adherence of the coating layer on the part, and at the same time lead to a lower coefficient of friction.
  • the coefficient of friction measured in the surface of the treated part after the second coating step is 50% lower to the one measured in the part after the first coating step and before the pickling.

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Laminated Bodies (AREA)

Abstract

Method for applying a phosphate coating on an iron or steel part, and corresponding iron or steel part. The method according to the invention consists in a first coating step with a first phosphating, through which a first crystalline layer of iron and manganese phosphates is obtained, an intermediate step of partial pickling of said first crystalline layer of phosphates, leaving the base metal partially uncovered, and a second coating step comprising a second phosphating through which a second crystalline layer of iron and manganese phosphates is obtained, covering the partially pickled first layer of phosphates and the base metal. The method provides a coating with a lower thickness, a finer crystallisation and a lower rugosity Rk than the one that can be obtained by a simple phosphating.

Description

METHOD FOR APPLYING A PHOSPHATE COATING ON A STEEL OR IRON PART, AND CORRESPONDING STEEL OR IRON PART
DESCRIPTION
Field of the invention
This invention relates to a method for applying a phosphate coating on a steel or iron part. The invention also relates to a steel or iron part obtained by said method.
State of the art Precision parts intended to undergo a sliding friction with high contact stress must be provided with an anti-friction coating which guarantees a high mechanical resistance and a low coefficient of friction. Manganese phosphate coatings, due to their high mechanical resistance, provide good results and thus they are commonly used in the finishing of steel or iron parts. Several methods for forming such coatings are known, being of special interest those consisting in immersing the part to be treated in an aqueous solution of manganese phosphate. It is known that by adding oxidation agents to the aqueous solution, finer coatings are obtained. On the other hand, it is known that using manganese phosphate solutions containing nitrate, and wherein the amount of nitrate in the form of NO3 " exceeds the quantity of phosphate in the form of PO4 3' , high density coatings having fine granulation and a thickness lower or equal to 5 μm are obtained. Furthermore, it is known that on iron surfaces, operating with low-density solutions, zinc or manganese phosphate coatings containing at least 1 % of nitrate and practically without ferrous iron can be obtained. When the aim is to obtain an anti-friction layer, generally it resorts to combined phospating processes, in particular of the type zinc- manganese, attempting to increase the ratio of manganese in the obtained deposits.
The mechanical industry requires to precision parts manufacturers a more and more perfect finishing, so that the anti-friction properties of the parts must be increasingly higher. However, in many cases the coatings obtained through the known methods described above do no reach such a finishing quality.
Summary of the invention
The invention aims to overcome this disadvantage. This purpose is achieved by a method for applying a phosphate coating on an iron or steel part, characterised in that it comprises:
- a first coating step comprising a first phosphating, through which on the base metal of said part a first crystalline layer of iron and manganese phosphates is obtained; - an intermediate step of partial pickling of said first crystalline layer of phosphates, leaving said base metal partially uncovered, and
- a second coating step comprising a second phosphating through which, on said partially pickled first crystalline layer of phosphates and on said partially uncovered base metal, a second crystalline layer of iron and manganese phosphates is obtained.
By means of this method according to the invention a coating with a particularly small thickness is achieved, having a particularly fine crystallisation with a high density of crystals by surface unit in the part surface. This leads, on the one hand, to a coefficient of friction much lower than the one that can be obtained by the known coating methods and, on the other hand, to a higher adherence of the coating on the part surface. In the method according to the invention, advantageously, a known coating method can be applied to carry out these first and second coating steps each one comprising a phosphating; in particular, said coating steps can comprise, typically, subsequent steps of treatment by immersing the part in a series of bathes, being these steps typically as follows : cleaning, degreasing, surface activating, phosphating, rinsing, drying and, optionally, greasing. The special feature of the method according to the invention is, therefore, the fact of having introduced a partial pickling step applied to the crystalline layer of phosphates which has been obtained by means of a coating method that may be one of the already known, as it has been said, and after that carrying out a new phosphating on said pickled layer. This intermediate pickling stage confers to the surface of the part a particular state that allows the second crystalline layer to be formed with better crystallographic features than the first one. Indeed, after the pickling the surface of the part has such a microstructure and activity that, when applying the second phosphating crystal, grains of phosphates are formed on the nucleation sites of said microstructure, growing with particularly reduced size and in an especially homogeneous form. This advantageous features of the part surface after the intermediate pickling step are precisely due to the fact that said pickling is partial, that is to say that on said surface the rest of the first crystalline layer and the base metal coexist. By applying the method according to the invention, it is obtained an iron or steel part with an iron and manganese phosphate coating characterised in that said coating has an homogeneous morphology with crystalline formations shaped as needles or columns of a size equal or lower than 2μm, having said coating a thickness equal or less than 2μm. Preferably, said coating has an apparent density higher or equal to 3 g/cm3 and lower or equal to 10 g/cm3 and, preferably, said coating has an specific weight higher or equal to 1.5 g/m2 and lower or equal to 7 g/m2 . The specific weight of coating, expressed in g/m2 , refers to the total mass of the coating deposited by surface unit. The apparent density of coating, expressed in g/cm3 , is defined as a ratio between the specific weight of the coating and the coating thickness. Preferably, said intermediate step of partial pickling consists in a mechanical pickling by erosion in an abrasive medium, by which it is obtained a surface finish suitable for growing the second layer of phosphates with the wished features of a lower grain size and a higher homogeneity. In particular, compared to other forms of pickling such as chemical pickling, mechanical pickling in an abrasive medium has the advantage of providing a partial pickling with a surface finish wherein the completely pickled surface of the base metal, that is, the surface completely free of phosphate crystals of the first layer, coexists with microcavities coated by phosphate crystals of the first layer which are firmly adhered to the metal substrate. This state is particularly advantageous for the growth of the second layer of phosphates with the wished features. Advantageously, said mechanical pickling by erosion in an abrasive medium lasts until at least 15% of the total surface of said first crystalline layer of phosphates had been completely pickled. In this way, a particularly fine and well adhered second layer of phosphates is obtained. Preferably, said mechanical pickling by erosion in an abrasive medium consists in a rotofinishing using ceramic abrasive with a continuous inflow of an aqueous solution comprising a surfactant and a chemical flocculation agent, having said aqueous solution a pH higher or equal to 6 and lower or equal to 10. By means of this particular method, the intermediate step of pickling provides a surface finish suitable for the grain growth during the second phosphating.
Advantageously, said first and second phosphatings consist in an immersion of said part in an acid solution comprising at least phosphoric acid, metallic acid phosphates, manganese, nickel, iron 2+ and nitrates, having said acid solution a total acid value higher or equal to 58 and lower or equal to 100 and a ratio between total acid and free acid higher or equal to 5 and lower or equal to 7, and being the content of iron 2+ in said acid solution lower or equal to 2.5 g/l. Regarding the concentrations indicated for the phosphating bath, the free acid is defined as the concentration of hydrogen ions corresponding to the first constant of dissociation of phosphoric acid not replaced by metallic ions, being expressed as millilitres or points of solution of NaOH 0.1 N which are necessary in order to achieve the neutralisation of said free acid from a sample of 10 ml of bath. By total acid it is understood the millilitres or points of NaOH 0.1N which are necessary in order to achieve the neutralisation corresponding to the equivalence point of secondary phosphates, phosphoric acid and primary phosphates present in a sample of 10 ml of bath, being also this value influenced by the precipitation of different metallic cations present in the bath. This method is able to advantageously generate a mixed crystalline phase of manganese and iron phosphates of hurealite type, which constitutes said first and second crystalline layers (although the second crystalline layer, as it has been said, has different crystallographic properties regarding the distribution and the grain size). Preferably, the immersion of said part in said acid solution is carried out by keeping said acid solution at a temperature higher or equal to 95°C and lower or equal to 98°C and it lasts while gas is released from the metallic surface of said part, whereby the formation of said step mixed crystalline phase is optimised and a well developed crystalline layer of phosphates is obtained. The invention further refers to a steel or iron part with a coating obtained according to the method of the invention, having said part the particular features described above.
Brief description of the drawings Other advantages and features of the invention are observed from the following description, wherein, without a limiting character, a preferred embodiment is presented, referring to the enclosed figures. The figures showing: Figs. 1a, 1b, 1c, 1d, 1e and 1f, images of electronic microscope showing, with a x1000 enlargement, the part surface after the intermediate step of partial pickling, which in this embodiment example consists in a rotofinishing; the different views correspond to different rotofinishing duration :
Fig 1a: 10 minutes Fig 1 b: 20 minutes Fig 1c: 30 minutes Fig 1d: 40 minutes Fig 1e: 50 minutes Fig 1f: 60 minutes
Figs. 2a, 2b, 2c, 2d, 2e and 2f, images of electronic microscope showing with a x5000 enlargement the morphology of the second crystalline layer after the second phosphating; the different images are surface views corresponding to the results obtained by rotofinishing durations in the intermediate step of partial pickling;
Fig. 2a: 10 minutes Fig. 2b: 20 minutes Fig. 2c: 30 minutes Fig. 2d: 40 minutes Fig. 2e: 50 minutes Fig. 2f: 60 minutes;
Figs. 3a and 3b, images of electronic microscope showing with a x5000 enlargement, in surface views, the morphology of the crystalline layer of phosphates; Fig. 3a corresponds to the results obtained after the first phosphating, while Fig. 3b corresponds to the results obtained after the second phosphating; Figs. 4a and 4b, images of electronic microscope similar to the ones of Figs. 3a and 3b, respectively, but in cross-sectional view; in this case, the image of Fig. 4a has a xδOOO enlargement and Fig. 4b has a x13000 enlargement;
Fig. 5, a comparative graphic of the thickness of the crystalline layer of phosphates, after the first phosphating and after the second phosphating; the total thickness of the coating e, expressed in μm, is represented in the axis of ordinates; the different points correspond to different measure points in the part surface; the points represented by a triangle correspond to the situation after the first phosphating, whereas the points represented by a filled circle correspond to the situation after the second phosphating;
Fig. 6a, a comparative graphic of the roughness Rk of the part surface, after the first phosphating and after the second phosphating; the roughness Rk, expressed in μm, is represented in the axis of ordinates; the different points correspond to different measure points in the part surface; the points represented by a triangle correspond to the situation after the first phosphating, whereas the points represented by a filled circle correspond to the situation after the second phosphating.
Detailed description of an embodiment of the invention
The method according to the invention is applied, as a non-limiting example, on a soft mechanised steel part subjected to a thermal treatment consisting in quenching and tempering. In this embodiment, said part is a recess for a roller used in pumps for injecting gas-oil at very high pressures and the applied method comprise the following steps:
1 ) First coating step, consisting in the following operations:
- Alkaline degreasing by immersion in a bath of deionized water with an additive of trade name "Ardrox 6514" commercialised by the firm Chemetall, at a temperature regulated between 65°C and 75°C and during a minimum period of time ranging from 5 to 6 minutes;
- Washing by a bath in water, without shaking, with a continuos renovation, at a temperature regulated between 35°C and 45°C and during a period of time ranging from 3 to 6 minutes;
- Activating the surface in order to facilitate the nucleation of phosphate crystals in the subsequent phosphating step, by means of a bath in a solution with additives of trade names "Gardolene V6560A" and "Gardolene V6561 B" commercialised by the firm Chemetall, containing sodium polyphosphates and insoluble crystals of manganese phosphate, applying an air flow ranging from 5 to 20 m3/h, at a temperature regulated between 20°C and 30°C and during a period of time ranging from 2 to 5 minutes;
- First phosphating by immersion in an acid solution formed by deionized water and an additive of trade name "Gardobond G4060" commercialised by the firm Chemetall, this solution comprising phosphoric acid, metallic acid phosphates, manganese, nickel, iron 2+ in a content lower than 2.5 g/l and nitrates, with a total acid value higher or equal to 58 and lower or equal to 100 and a ratio between total acid and free acid ranging from 95°C to 98°C and during a period of time ranging from 3 to 5 minutes;
-Washing by a bath in water, without shaking, at a temperature regulated between 35°C and 45°C and during a period of time ranging from 3 to 6 minutes;
- Drying by immersion in a bath of hydrofuging oil;
obtaining, after this first coating step, a first crystalline layer of iron and manganese phosphates.
2) Intermediate step of partial pickling of said first crystalline layer of phosphates, consisting in a mechanical pickling by erosion in an abrasive medium by means of rotofinishing using ceramic abrasive, with a continuos inflow of aqueous solution comprising a surfactant and a chemical flocculation agent, having said aqueous solution a pH higher or equal to 6 and lower or equal to 10, and carrying out said mechanical pickling operation at room temperature and during a period of time of 30 minutes, being completely pickled, that is, leaving the base metal uncovered, 60% of the total initial surface of the first crystalline layer of phosphates.
3) Second coating step, comprising a second phosphating and being identical to the first coating step, obtaining on said first crystalline layer of phosphates partially pickled a second crystalline layer of iron and manganese phosphates.
The morphological features of the second crystalline layer of phosphates mainly depends on the time of mechanical pickling of the first crystalline layer of phosphates, that is, the percentage of surface which is completely pickled, as it can be seen in Figs. 1a-1f and 2a-2f. In the case of the part treated in this example, this percentage amounts to 60%. However, depending on the type of part to be treated and on the wished results, a lower or higher time for pickling can be applied in order to obtain a higher or lower percentage of completely pickled surface. It has been observed, nevertheless, that a particularly good result is obtained when this percentage is higher or equal to 15%, even though with a lower percentage satisfactory results, in any case higher than the ones of the methods of the prior art, can be obtained.
The first coating step, as described above, corresponds per se to a method for obtaining a coating by phosphating according to the state of the prior art. Figs. 3a, 3b, 4a, 4b, 5 and 6 show that the method according to the invention provides a coating of a much higher quality than the one that can be obtained by a method of the prior art, that is applying simply a first coating step. In particular, in Figs. 3a, 3b and 4a, 4b can be observed that the crystallographic features of the coating layer after the second phosphating are completely different from the ones observed after the first phosphating. In fact, after the second phosphating the size of the grain is much lower, crystals are more homogeneous and have a crystalline structure with a morphology shaped as fine needles with a size lower or equal to 2 μm, whereas after the first phosphating crystals had a crystalline structure with a typically polyhedral morphology and a size reaching until 10 μm. In Figs. 5 and 6 can also be observed that the coating layer obtained after the second coating step has a remarkably lower thickness and a much lower roughness than the layer obtained after the first coating step. The decrease of the crystal size as well as its higher density imply a higher adherence of the coating layer on the part, and at the same time lead to a lower coefficient of friction. In fact, in this example, the coefficient of friction measured in the surface of the treated part after the second coating step is 50% lower to the one measured in the part after the first coating step and before the pickling.

Claims

1.- Method for applying a phosphate coating on an iron or steel part, being characterised said method in that it comprises: - a first coating step comprising a first phosphating, through which on the base metal of said part a first crystalline layer of iron and manganese phosphates is obtained; - an intermediate step of partial pickling of said first crystalline layer of phosphates, leaving said base metal partially uncovered, and - a second coating step comprising a second phosphating through which, on said partially pickled first crystalline layer of phosphates and on said partially uncovered base metal, a second crystalline layer of iron and manganese phosphates is obtained .
2.- Method according to claim 1 , characterised in that said intermediate step of partial pickling consists in a mechanical pickling by erosion in an abrasive medium.
3.- Method according to claim 2, characterised in that said mechanical pickling by erosion in an abrasive medium lasts until at least 15% of the total surface of said first crystalline layer of phosphates had been completely pickled.
4.- Method according to claim 3, characterised in that said mechanical pickling by erosion in an abrasive medium consists in a rotofinishing using ceramic abrasive with a continuos inflow of an aqueous solution comprising a surfactant and a chemical flocculation agent, having said aqueous solution a pH higher or equal to 6 and lower or equal to 10. 5. Method according to any of claims 1 to 4, characterised in that said first and second phosphatings consist in an immersion of said part in an acid solution comprising at least phosphoric acid, metallic acid phosphates, manganese, nickel, iron 2+ and nitrates, having said acid solution a total acid value higher or equal to 58 and lower or equal to 100 and a ratio between total acid and free acid higher or equal to 5 and lower or equal to 7, and being the content of iron 2+ in said acid solution lower or equal to 2.
5 g/l.
6.- Method according to claim 5, characterised in that the immersion of said part in said acid solution is carried out by keeping said acid solution at a temperature higher or equal to 95°C and lower or equal to 98°C and it lasts while gas is released from the metallic surface of said part.
7.- Iron or steel part with an iron and manganese phosphate coating, characterised in that said coating has an homogeneous morphology with crystalline forms shaped as needles or columns of a size lower or equal to 2μm, having said coating a thickness lower or equal to
2μm.
8. Part according to claim 7, characterised in that said coating has an apparent density higher or equal to 3 g/cm3 and lower or equal to 10 g/cm3 .
9. Part according to claim 8, characterised in that said coating has an specific weight higher or equal to 1.5 g/m2 and lower or equal to 7 g/ m2
PCT/EP2005/003911 2004-05-04 2005-04-11 Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part WO2005106074A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP05759114A EP1660699A1 (en) 2004-05-04 2005-04-11 Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part
US10/570,778 US20080264523A1 (en) 2004-05-04 2005-04-11 Method for Applying a Phosphate Coating on a Steel or Iron Part, and Corresponding Steel or Iron Part

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200401059A ES2213500B1 (en) 2004-05-04 2004-05-04 PROCEDURE FOR OBTAINING A COATING BY PHOSPHATED IN AN IRON OR STEEL PIECE, AND CORRESPONDING IRON OR STEEL PIECE.
ES200401059 2004-05-04

Publications (2)

Publication Number Publication Date
WO2005106074A1 true WO2005106074A1 (en) 2005-11-10
WO2005106074A8 WO2005106074A8 (en) 2006-03-09

Family

ID=32921836

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2005/003911 WO2005106074A1 (en) 2004-05-04 2005-04-11 Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part

Country Status (4)

Country Link
US (1) US20080264523A1 (en)
EP (1) EP1660699A1 (en)
ES (1) ES2213500B1 (en)
WO (1) WO2005106074A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2213500B1 (en) * 2004-05-04 2005-05-01 Delphi Diesel Systems S.L. PROCEDURE FOR OBTAINING A COATING BY PHOSPHATED IN AN IRON OR STEEL PIECE, AND CORRESPONDING IRON OR STEEL PIECE.
CN106521466B (en) * 2016-09-18 2019-06-04 山东大学 The preparation method of titanium or titanium alloy surface chemical composition coating is induced using electric coupling

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1390957A (en) * 1971-05-10 1975-04-16 Craig Investments Pty Ltd S Rust proofing process
GB1408604A (en) * 1972-09-29 1975-10-01 Vaq Fos Ltd Method of phosphating metal surfaces
JPS5528332A (en) * 1978-08-17 1980-02-28 Masaji Hojo Simultaneous surface finishing and compound coating method for metallic work piece by barreling
WO2002062528A2 (en) * 2001-02-08 2002-08-15 Rem Technologies, Inc. Chemical mechanical machining and surface finishing
ES2213500A1 (en) * 2004-05-04 2004-08-16 Delphi Diesel Systems S.L. Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3071456A (en) * 1956-02-08 1963-01-01 William D Cheesman Barrel finishing
DE3800834A1 (en) * 1988-01-14 1989-07-27 Henkel Kgaa METHOD AND MEANS FOR SIMULTANEOUS SLICING, CLEANING AND PASSIVATING OF METALLIC WORKSTUFFS
JPH02173274A (en) * 1988-12-24 1990-07-04 Kobe Steel Ltd Method for phosphating galvanized steel sheet
US5588989A (en) * 1994-11-23 1996-12-31 Ppg Industries, Inc. Zinc phosphate coating compositions containing oxime accelerators
US6039891A (en) * 1996-09-24 2000-03-21 Cabot Corporation Multi-oxidizer precursor for chemical mechanical polishing

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1390957A (en) * 1971-05-10 1975-04-16 Craig Investments Pty Ltd S Rust proofing process
GB1408604A (en) * 1972-09-29 1975-10-01 Vaq Fos Ltd Method of phosphating metal surfaces
JPS5528332A (en) * 1978-08-17 1980-02-28 Masaji Hojo Simultaneous surface finishing and compound coating method for metallic work piece by barreling
WO2002062528A2 (en) * 2001-02-08 2002-08-15 Rem Technologies, Inc. Chemical mechanical machining and surface finishing
ES2213500A1 (en) * 2004-05-04 2004-08-16 Delphi Diesel Systems S.L. Method for applying a phosphate coating on a steel or iron part, and corresponding steel or iron part

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
NITTEL K-D: "MANGANPHOSPHATIERUNG QUALITAETSVERBESSERUNG UND KOSTENEINSPARUNG MIT MODERNEN VERFAHREN", MO METALLOBERFLACHE, HANSER, MUNCHEN, DE, vol. 53, no. 9, September 1999 (1999-09-01), pages 23 - 24,26, XP000854002, ISSN: 0026-0797 *
PATENT ABSTRACTS OF JAPAN vol. 004, no. 061 (C - 009) 8 May 1980 (1980-05-08) *

Also Published As

Publication number Publication date
ES2213500B1 (en) 2005-05-01
EP1660699A1 (en) 2006-05-31
US20080264523A1 (en) 2008-10-30
WO2005106074A8 (en) 2006-03-09
ES2213500A1 (en) 2004-08-16

Similar Documents

Publication Publication Date Title
Kouisni et al. Phosphate coatings on magnesium alloy AM60: Part 2: Electrochemical behaviour in borate buffer solution
US4419199A (en) Process for phosphatizing metals
Takács et al. Effects of pre-treatments on the corrosion properties of electroless Ni–P layers deposited on AlMg2 alloy
JPH01123080A (en) Zinc phosphate type film treatment method and solution, and replenishing agent
JP2019510886A (en) Improved method for phosphating metal surfaces without nickel
US20160376690A1 (en) Phosphating or anodizing for improved bonding of thermal spray coating on engine cylinder bores
JPH04506233A (en) Method for forming zinc phosphate film containing manganese and magnesium
JP2002294466A (en) Conversion coating solution for magnesium alloy, surface treatment method, and magnesium-alloy base material
US4681641A (en) Alkaline resistant phosphate conversion coatings
EP0452638B1 (en) Method for phosphating metal surfaces
Moradi et al. Electroless plating of Sn/Cu/Zn triple layer on AA6082 aluminum alloy
US20080264523A1 (en) Method for Applying a Phosphate Coating on a Steel or Iron Part, and Corresponding Steel or Iron Part
Burokas et al. The influence of hexametaphosphate on formation of zinc phosphate coatings for deep drawing of steel tubes
WO2010092579A1 (en) A process for electroplating of copper
US6179934B1 (en) Aqueous phosphating composition and process for metal surfaces
EP0102284B1 (en) Composition and process for the chemical conversion of metallic substrates
Bogi et al. Phosphate conversion coatings on steel
DE4032232A1 (en) METHOD FOR PRODUCING ALUMINUM DISK STORAGE WITH SMOOTH, METAL-PLATED SURFACES
JPH10204649A (en) Aqueous phosphate treating solution for metallic surface and its treatment
US5045130A (en) Solution and process for combined phosphatization
US5954892A (en) Method and composition for producing zinc phosphate coatings on metal surfaces
JPH08319557A (en) Method for modifying surface of steel utilizing diffusing dilution of aluminum
US3547711A (en) Process for coating ferrous surfaces
JP2003277959A (en) Hot rolled steel sheet having excellent chemical conversion treatability and method for manufacturing the same
US4722753A (en) Alkaline resistant phosphate conversion coatings

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2005759114

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 10570778

Country of ref document: US

CFP Corrected version of a pamphlet front page
CR1 Correction of entry in section i

Free format text: IN PCT GAZETTE 45/2005 UNDER (71) THE ADDRESS SHOULD READ "CTRA. DE CERDANYOLA 97-101, E-08190 SANTCUGAT DEL VALLèS (BARCELONA) (ES)."; UNDER (72, 75) THE NAME SHOULD READ "VARELA LOSADA, FRANCISCO"

WWP Wipo information: published in national office

Ref document number: 2005759114

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE