EP0056675B1 - Pretreatment composition for phosphatising ferrous metals, and method of preparing the same - Google Patents
Pretreatment composition for phosphatising ferrous metals, and method of preparing the same Download PDFInfo
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- EP0056675B1 EP0056675B1 EP82200062A EP82200062A EP0056675B1 EP 0056675 B1 EP0056675 B1 EP 0056675B1 EP 82200062 A EP82200062 A EP 82200062A EP 82200062 A EP82200062 A EP 82200062A EP 0056675 B1 EP0056675 B1 EP 0056675B1
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- titanium
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- 239000000203 mixture Substances 0.000 title claims abstract description 53
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 22
- 239000002184 metal Substances 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 title claims description 17
- -1 ferrous metals Chemical class 0.000 title claims description 14
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 14
- 239000010452 phosphate Substances 0.000 claims abstract description 14
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims abstract description 11
- 150000003609 titanium compounds Chemical class 0.000 claims abstract description 10
- 235000011180 diphosphates Nutrition 0.000 claims abstract description 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims abstract description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000010936 titanium Substances 0.000 claims abstract description 5
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 5
- 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 claims description 18
- 229910000165 zinc phosphate Inorganic materials 0.000 claims description 18
- 238000002360 preparation method Methods 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000008247 solid mixture Substances 0.000 claims description 14
- 229910052783 alkali metal Inorganic materials 0.000 claims description 11
- 239000000243 solution Substances 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 238000007746 phosphate conversion coating Methods 0.000 claims description 9
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 229940005654 nitrite ion Drugs 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 4
- 230000002401 inhibitory effect Effects 0.000 claims description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 4
- HDUMBHAAKGUHAR-UHFFFAOYSA-J titanium(4+);disulfate Chemical compound [Ti+4].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O HDUMBHAAKGUHAR-UHFFFAOYSA-J 0.000 claims description 3
- 239000008199 coating composition Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 10
- 238000004381 surface treatment Methods 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 229910052700 potassium Inorganic materials 0.000 description 6
- 229940048084 pyrophosphate Drugs 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 238000007739 conversion coating Methods 0.000 description 3
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 3
- CADNYOZXMIKYPR-UHFFFAOYSA-B ferric pyrophosphate Chemical compound [Fe+3].[Fe+3].[Fe+3].[Fe+3].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O CADNYOZXMIKYPR-UHFFFAOYSA-B 0.000 description 3
- 229940005657 pyrophosphoric acid Drugs 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 239000010960 cold rolled steel Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- JUWGUJSXVOBPHP-UHFFFAOYSA-B titanium(4+);tetraphosphate Chemical compound [Ti+4].[Ti+4].[Ti+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O JUWGUJSXVOBPHP-UHFFFAOYSA-B 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- NFOVOLLZYFKJCK-UHFFFAOYSA-J [Fe+4].[O-]P([O-])(=O)OP([O-])([O-])=O Chemical group [Fe+4].[O-]P([O-])(=O)OP([O-])([O-])=O NFOVOLLZYFKJCK-UHFFFAOYSA-J 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000006174 pH buffer Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 150000003864 primary ammonium salts Chemical class 0.000 description 1
- 150000003865 secondary ammonium salts Chemical class 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 150000003866 tertiary ammonium salts Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- 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
- C23C22/78—Pretreatment of the material to be coated
- C23C22/80—Pretreatment of the material to be coated with solutions containing titanium or zirconium compounds
Definitions
- This invention relates to an aqueous solution for the treatment of ferrous metal surfaces, to the treatment of ferrous metal surfaces with this aqueous solution, to a solid composition suitable for preparing the aqueous solution and to the production of the solid composition.
- the usual treatment steps include the following in order: (1) degreasing; (2) washing with water; (3) surface preparation; (4) conversion coating; (5) washing with water; (6) drying; and (7) siccative coating.
- surface preparation step various proposals have hitherto been made.
- Japanese Patent Publication Number 7125/1964 discloses the use of a surface preparation composition which is produced by dissolving a titanium oxide with an excess quantity of sulphuric acid, adding thereto phosphoric acid or an alkali metal salt thereof, and/or pyrophosphoric acid or its alkali metal salt to form a slurry at pH of 1 or lower, followed by ageing the slurry at a pH of from 6.5 to 8.5.
- This surface preparation composition is reported to contribute to the precipitation of the zinc phosphate coating in the conversion coating step which follows.
- this composition does not provide the desired microcrystalline coating in the zinc phosphate conversion coating treatment.
- the present invention relates to surface preparation compositions for the treatment of ferrous metal surfaces that do not suffer from the disadvantages of the prior art composition discussed above.
- the surface preparation compositions of the present invention can be used for long periods of time and such use results in a uniform and dense zinc phosphate coating when a zinc phosphate conversion coating composition is applied to the surface so treated.
- the surface preparation compositions of the invention can be used to pretreat any ferrous metal surface, such as steel or other alloys of iron where the alloy consists predominantly of iron.
- composition for the treatment of ferrous metal surfaces which composition is an aqueous solution comprising:
- a rust-inhibiting quantity of nitrite ion e.g. in the form of its alkali metal salt, such as the sodium or potassium salt, may be added to the solution, provided the quantity added is not so large as to interfere with the effectiveness of the compositions.
- various compounds may be employed. Examples of such compounds include titanium sulphate or titanium oxide as a source of (a); phosphoric acid, a primary alkali metal salt (e.g. Na or K salt) or primary ammonium salt of phosphoric acid, a secondary alkali metal salt (e.g. Na or K salt) or secondary ammonium salt of phosphoric acid, or a tertiary alkali metal salt (e.g. Na or K salt) or tertiary ammonium salt of phosphoric acid as a source of (b); pyrophosphoric acid or an alkali metal salt (e.g.
- Na or K salt or ammonium salt of pyrophosphoric acid as a source of (c); and carbonic acid, an alkali metal salt (e.g. Na or K salt) or ammonium salt of carbonic acid, alkali metal hydrogen carbonate (e.g. Na or K salt) or ammonium hydrogen carbonate as a source of (d).
- an alkali metal salt e.g. Na or K salt
- ammonium salt of carbonic acid e.g. Na or K salt
- alkali metal hydrogen carbonate e.g. Na or K salt
- ammonium hydrogen carbonate e.g. Na or K salt
- the present invention also relates to solid compositions (conveniently in powder form) that can be added to water to form the aqueous pretreatment compositions of the invention.
- solid compositions comprise:
- a small quanity of nitrite ion can also be present to provide a rust-inhibiting quantity of nitrite ion when the solid compositions are diluted with a sufficient quantity of water to give the aqueous pretreatment compositions of the invention.
- the solid compositions can be prepared by (A) mixing the sources of titanium compound, phosphate and/or acid phosphate, and pyrophosphate together with water in the above proportions; (B) heating the resulting mixture, e.g. at a temperature in the range of from 100° to 120°C until the water content is substantially removed, e.g. to a level of 1.5% by weight or less; and (C) mixing, which should be even mixing, the resulting solid residue with the source of carbonate and/or acid carbonate added in the above proportion.
- a titanium phosphate colloid adheres thereto, which serves to accelerate the formation of a zinc phosphate conversion coating by providing crystal nuclei around which the zinc phosphate coating can form.
- the resulting zinc phosphate coating has excellent characteristics as a base for siccative coatings such as paint.
- the titanium compound concentration is lower than the amount specified, the colloid which becomes the crystal nuclei for the zinc phosphate coating is formed in too small a quantity.
- the titanium compound concentration is higher than the amount specified, no enhanced effect is obtained.
- the phosphate and/or acid phosphate concentration specified is also present for the same purpose, i.e. to provide an adequate quantity of titanium phosphate colloid on the ferrous metal surface.
- the pyrophosphate has the beneficial effect of micronizing the zinc phosphate conversion coating.
- concentration of pyrophosphate is below the range specified, adequate micronizing is not achieved.
- concentration is above the range specified, the pyrophosphate tends to react with the iron in the ferrous metal surface, resulting in the inhibition of formation of a zinc phosphate conversion coating.
- the pH buffer effect is not obtained, i.e. when the pH of the present aqueous pretreatment composition is lower than the required values, the pyrophosphate ion tends to react with the ferrous metal surface, resulting in the inhibition of the subsequent zinc phosphate conversion coating formation.
- too high a pH value does not give a preferred conversion coating for pretreatments of electro coating.
- aqueous surface preparation compositions When the present aqueous surface preparation compositions are used in the pretreatment of ferrous metal surfaces, such compositions can be used for long periods of time, and provide a base for uniform, dense zinc phosphate conversion coatings.
- the surface preparation compositions of the present invention are especially effective for preparing ferrous metal surfaces for zinc phosphate treatment for electro coating.
- the long-term stability of the instant surface preparation compositions is particularly advantageous in the dipping type treatment of metals in which a large quantity of surface preparation composition is employed.
- An aqueous surface treatment composition was prepared using the following quantities of ingredients:
- An aqueous surface treatment composition was prepared using the following quantities of ingredients:
- a solid mixture was formed in accordance with the process of Example I, and the mixture was added to sufficient water to give a solution of 0.1% concentration.
- aqueous surface treatment composition was prepared from the following ingredients using the procedure of Example I, except that the solid mixture formed was diluted with water to form a 0.05% aqueous solution:
- Each of three degreased commercial cold rolled steel plates was treated with one of the new aqueous compositions of Examples I, II and III, i.e. one plate was treated with the composition of Example I, a second plate with the composition of Example II, etc.
- the plates were treated by dipping them for 1 minute in the aqueous composition, allowing excess liquid to drip off, and immediately dipping them into a zinc phosphate conversion coating bath (Nippon Paint Co. "GRANODINE SD 2000”) for 2 minutes at a bath temperature of 50°C.
- the plates were then washed with water, dried, and evaluated; in addition, the above procedure was repeated with an additional three steel plates after the aqueous compositions of Examples I, II and III had stood for 10 days.
- the results obtained are given in the Table below Example VIII, together with the pH values of the pretreatment compositions.
- An aqueous surface treatment composition was prepared from the following ingredients:
- Example II A solid mixture was formed from the above ingredients in accordance with the procedure of Example I (except that all of the above ingredients were mixed together and heated to form the solid mixture). A 0.05% aqueous solution was formed according to the procedure of Example I.
- An aqueous surface treatment composition was prepared from the following ingredients in accordance with the procedure of Example V except that the solid mixture was diluted with water to form a 0.1% aqueous solution.
- An aqueous surface treatment composition was prepared from the following ingredients in accordance with the procedure of Example V except that the solid mixture was diluted with water to form a 0.07% aqueous solution.
- Example IV Six degreased commercial cold rolled steel plates of the type used in Example IV were treated according to the procedure of Example IV. The results obtained are given in the Table below for comparison purposes.
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- 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)
Abstract
Description
- This invention relates to an aqueous solution for the treatment of ferrous metal surfaces, to the treatment of ferrous metal surfaces with this aqueous solution, to a solid composition suitable for preparing the aqueous solution and to the production of the solid composition.
- In the surface treatment of ferrous metals such as steel and other alloys of iron, the usual treatment steps include the following in order: (1) degreasing; (2) washing with water; (3) surface preparation; (4) conversion coating; (5) washing with water; (6) drying; and (7) siccative coating. With respect to the surface preparation step, various proposals have hitherto been made. For example, Japanese Patent Publication Number 7125/1964 discloses the use of a surface preparation composition which is produced by dissolving a titanium oxide with an excess quantity of sulphuric acid, adding thereto phosphoric acid or an alkali metal salt thereof, and/or pyrophosphoric acid or its alkali metal salt to form a slurry at pH of 1 or lower, followed by ageing the slurry at a pH of from 6.5 to 8.5. This surface preparation composition is reported to contribute to the precipitation of the zinc phosphate coating in the conversion coating step which follows. However, when the pH of said composition is about 8.5 or lower, pyrophosphate ion in the composition reacts with the ferrous metal surface to form an iron pyrophosphate coating on the surface thereof, which inhibits the formation of the zinc phosphate coating, this causing unevenness in treatment. Also, the pH of the surface preparation composition decreases with the passage of time for some unknown reason, and as a result, iron pyrophosphate forms on the surface of the ferrous metals treated with the composition. Furthermore even where the pH of the composition is adjusted to a pH, e.g. about 9, where iron pyrophosphate does not precipitate, such as by the addition of caustic soda, caustic potash, etc., the pH still decreases after a short period of time, causing the problem of iron pyrophosphate coating on the surface of the metals being treated. Accordingly, pH control of this prior art composition is difficult, and satisfactory surface preparations cannot be carried out with the compositions over long periods of time. Frequent replacements of the compositions must be made, with attendant expense and down time, particularly since the usual dipping process involves the use of large quantities of the surface preparation compositions.
- In addition to the above problem with the prior art surface preparation composition, this composition does not provide the desired microcrystalline coating in the zinc phosphate conversion coating treatment.
- The present invention relates to surface preparation compositions for the treatment of ferrous metal surfaces that do not suffer from the disadvantages of the prior art composition discussed above. The surface preparation compositions of the present invention can be used for long periods of time and such use results in a uniform and dense zinc phosphate coating when a zinc phosphate conversion coating composition is applied to the surface so treated.
- The surface preparation compositions of the invention can be used to pretreat any ferrous metal surface, such as steel or other alloys of iron where the alloy consists predominantly of iron.
- The invention provides a composition for the treatment of ferrous metal surfaces, which composition is an aqueous solution comprising:
- (a) titanium compound in amount from 1 to 100 parts per million by weight, measured as titanium;
- (b) phosphate and/or acid phosphate in amount totalling from 50 to 1500 parts per million by weight, measured as P04;
- (c) pyrophosphate in amount from 10 to 300 parts per million by weight, measured as P 2°7; and
- (d) carbonate and/or acid carbonate in amount totalling 20 to 1500 parts per million by weight, measured as C03;
- Optionally, a rust-inhibiting quantity of nitrite ion, e.g. in the form of its alkali metal salt, such as the sodium or potassium salt, may be added to the solution, provided the quantity added is not so large as to interfere with the effectiveness of the compositions.
- As sources for the essential ingredients, various compounds may be employed. Examples of such compounds include titanium sulphate or titanium oxide as a source of (a); phosphoric acid, a primary alkali metal salt (e.g. Na or K salt) or primary ammonium salt of phosphoric acid, a secondary alkali metal salt (e.g. Na or K salt) or secondary ammonium salt of phosphoric acid, or a tertiary alkali metal salt (e.g. Na or K salt) or tertiary ammonium salt of phosphoric acid as a source of (b); pyrophosphoric acid or an alkali metal salt (e.g. Na or K salt) or ammonium salt of pyrophosphoric acid as a source of (c); and carbonic acid, an alkali metal salt (e.g. Na or K salt) or ammonium salt of carbonic acid, alkali metal hydrogen carbonate (e.g. Na or K salt) or ammonium hydrogen carbonate as a source of (d).
- The present invention also relates to solid compositions (conveniently in powder form) that can be added to water to form the aqueous pretreatment compositions of the invention. Such solid compositions comprise:
- (a) titanium compound in amount from 1 to 100 parts by weight, measured as titanium;
- (b) phosphate and/or acid phosphate in amount totalling from 50 to 1500 parts by weight, measured as P0 4 ;
- (c) pyrophosphate in amount from 10 to 300 parts by weight, measured as P207; and
- (d) carbonate and/or acid carbonate in amount totalling 20 to 1500 parts by weight, measured as C03.
- Optionally, a small quanity of nitrite ion can also be present to provide a rust-inhibiting quantity of nitrite ion when the solid compositions are diluted with a sufficient quantity of water to give the aqueous pretreatment compositions of the invention.
- The solid compositions can be prepared by (A) mixing the sources of titanium compound, phosphate and/or acid phosphate, and pyrophosphate together with water in the above proportions; (B) heating the resulting mixture, e.g. at a temperature in the range of from 100° to 120°C until the water content is substantially removed, e.g. to a level of 1.5% by weight or less; and (C) mixing, which should be even mixing, the resulting solid residue with the source of carbonate and/or acid carbonate added in the above proportion.
- When ferrous metal surfaces are treated with the aqueous compositions of the invention, a titanium phosphate colloid adheres thereto, which serves to accelerate the formation of a zinc phosphate conversion coating by providing crystal nuclei around which the zinc phosphate coating can form. The resulting zinc phosphate coating has excellent characteristics as a base for siccative coatings such as paint. When the titanium compound concentration is lower than the amount specified, the colloid which becomes the crystal nuclei for the zinc phosphate coating is formed in too small a quantity. When the titanium compound concentration is higher than the amount specified, no enhanced effect is obtained. The phosphate and/or acid phosphate concentration specified is also present for the same purpose, i.e. to provide an adequate quantity of titanium phosphate colloid on the ferrous metal surface.
- The pyrophosphate has the beneficial effect of micronizing the zinc phosphate conversion coating. When the concentration of pyrophosphate is below the range specified, adequate micronizing is not achieved. When its concentration is above the range specified, the pyrophosphate tends to react with the iron in the ferrous metal surface, resulting in the inhibition of formation of a zinc phosphate conversion coating.
- When the carbonate and/or acid carbonate is employed in a quantity lower than that specified, the pH buffer effect is not obtained, i.e. when the pH of the present aqueous pretreatment composition is lower than the required values, the pyrophosphate ion tends to react with the ferrous metal surface, resulting in the inhibition of the subsequent zinc phosphate conversion coating formation. On the other hand, too high a pH value does not give a preferred conversion coating for pretreatments of electro coating.
- When the present aqueous surface preparation compositions are used in the pretreatment of ferrous metal surfaces, such compositions can be used for long periods of time, and provide a base for uniform, dense zinc phosphate conversion coatings. The surface preparation compositions of the present invention are especially effective for preparing ferrous metal surfaces for zinc phosphate treatment for electro coating. The long-term stability of the instant surface preparation compositions is particularly advantageous in the dipping type treatment of metals in which a large quantity of surface preparation composition is employed.
- The invention is illustrated by the following Examples, in which the term "%" refers to percent by weight.
-
- The above ingredients, except for the sodium bicarbonate, were heated at a temperature maintained in the range of 100° to 120°C with stirring until the water content was reduced to 1.5% or lower (about 2 hours). To the powder so obtained, the sodium bicarbonate was added and evenly mixed together.
- The above solid mixture was then diluted with sufficient water to give a solution having a concentration of 0.07% of the mixture.
-
- A solid mixture was formed in accordance with the process of Example I, and the mixture was added to sufficient water to give a solution of 0.1% concentration.
-
- Each of three degreased commercial cold rolled steel plates was treated with one of the new aqueous compositions of Examples I, II and III, i.e. one plate was treated with the composition of Example I, a second plate with the composition of Example II, etc. The plates were treated by dipping them for 1 minute in the aqueous composition, allowing excess liquid to drip off, and immediately dipping them into a zinc phosphate conversion coating bath (Nippon Paint Co. "GRANODINE SD 2000") for 2 minutes at a bath temperature of 50°C. The plates were then washed with water, dried, and evaluated; in addition, the above procedure was repeated with an additional three steel plates after the aqueous compositions of Examples I, II and III had stood for 10 days. The results obtained are given in the Table below Example VIII, together with the pH values of the pretreatment compositions.
- The following Examples are given for comparison purposes, using aqueous surface treatment compositions in accordance with the teachings of the prior art.
-
- A solid mixture was formed from the above ingredients in accordance with the procedure of Example I (except that all of the above ingredients were mixed together and heated to form the solid mixture). A 0.05% aqueous solution was formed according to the procedure of Example I.
-
-
-
- Evaluation criteria used in the above Table for the appearance of treated surfaces:
- 0: Formation of uniform and dense zinc phosphate coating.
- A: Unevenness in zinc phosphate coating.
- X: Yellow rust; tempering observed.
the solution having a pH from 8.5 to 9.5.
Claims (13)
the solution having a pH from 8.5 to 9.5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT82200062T ATE10513T1 (en) | 1981-01-19 | 1982-01-19 | PRETREATMENT COMPOSITION FOR THE PHOSPHATION OF FERROUS METALS AND PROCESS FOR THE PRODUCTION THEREOF. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7028/81 | 1981-01-19 | ||
JP56007028A JPS5855229B2 (en) | 1981-01-19 | 1981-01-19 | Surface conditioner for zinc phosphate treatment |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0056675A2 EP0056675A2 (en) | 1982-07-28 |
EP0056675A3 EP0056675A3 (en) | 1982-08-04 |
EP0056675B1 true EP0056675B1 (en) | 1984-11-28 |
Family
ID=11654577
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82200062A Expired EP0056675B1 (en) | 1981-01-19 | 1982-01-19 | Pretreatment composition for phosphatising ferrous metals, and method of preparing the same |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0056675B1 (en) |
JP (1) | JPS5855229B2 (en) |
AT (1) | ATE10513T1 (en) |
DE (1) | DE3261311D1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61257481A (en) * | 1985-05-10 | 1986-11-14 | Nippon Parkerizing Co Ltd | Aqueous solution for surface conditioning for forming phosphate film by chemical conversion treatment |
JPS6343039U (en) * | 1986-09-06 | 1988-03-22 | ||
CA1309315C (en) * | 1987-07-14 | 1992-10-27 | Toan Manh Ngo | Compositions and process for metal treatment |
DE3814363A1 (en) * | 1988-04-28 | 1989-11-09 | Henkel Kgaa | TITANIUM-FREE ACTIVATING AGENTS, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR ACTIVATING METAL SURFACES BEFORE ZINC PHOSPHATING |
US5112395A (en) * | 1989-02-22 | 1992-05-12 | Monsanto Company | Compositions and process for metal treatment |
US5026423A (en) * | 1989-02-22 | 1991-06-25 | Monsanto Chemical Company | Compositions and process for metal treatment |
JPH0394075A (en) * | 1989-09-04 | 1991-04-18 | Nippon Parkerizing Co Ltd | Surface conditioning treatment |
TWI224629B (en) * | 2002-07-31 | 2004-12-01 | Nippon Steel Corp | Resin-lined steel pipe and method for manufacturing same |
EP3371345B1 (en) | 2015-11-04 | 2020-05-20 | Illinois Tool Works Inc. | Corrosion inhibitor and water conditioning agent |
MX2019001874A (en) | 2016-08-24 | 2019-06-06 | Ppg Ind Ohio Inc | Alkaline composition for treating metal substartes. |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE885638C (en) * | 1945-02-27 | 1953-08-06 | Metallgesellschaft Ag | Process for the production of a pre-wash solution for phosphating |
US2490062A (en) * | 1949-01-21 | 1949-12-06 | Westinghouse Electric Corp | Cleaning and activating compositions and use thereof in producing protective phosphate coatings on metal surfaces |
GB774667A (en) * | 1955-12-01 | 1957-05-15 | John Arthur Kemp | Improvements in or relating to the phosphate coating of metal surfaces |
FR1291347A (en) * | 1961-06-06 | 1962-04-20 | Parker Ste Continentale | Iron and steel spray phosphating process |
US3728163A (en) * | 1970-05-25 | 1973-04-17 | Balm Paints Ltd | Alkaline liquids for cleaning metals |
BE789347A (en) * | 1971-09-30 | 1973-01-15 | Amchem Prod | Methods and compositions for the treatment of ferrous and zinc surfaces |
-
1981
- 1981-01-19 JP JP56007028A patent/JPS5855229B2/en not_active Expired
-
1982
- 1982-01-19 AT AT82200062T patent/ATE10513T1/en not_active IP Right Cessation
- 1982-01-19 EP EP82200062A patent/EP0056675B1/en not_active Expired
- 1982-01-19 DE DE8282200062T patent/DE3261311D1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
ATE10513T1 (en) | 1984-12-15 |
EP0056675A2 (en) | 1982-07-28 |
JPS5855229B2 (en) | 1983-12-08 |
JPS57120678A (en) | 1982-07-27 |
EP0056675A3 (en) | 1982-08-04 |
DE3261311D1 (en) | 1985-01-10 |
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