US2528787A - Protection of metals from corrosion - Google Patents
Protection of metals from corrosion Download PDFInfo
- Publication number
- US2528787A US2528787A US772894A US77289447A US2528787A US 2528787 A US2528787 A US 2528787A US 772894 A US772894 A US 772894A US 77289447 A US77289447 A US 77289447A US 2528787 A US2528787 A US 2528787A
- Authority
- US
- United States
- Prior art keywords
- calcium
- phosphate
- metal
- articles
- film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 229910052751 metal Inorganic materials 0.000 title claims description 61
- 239000002184 metal Substances 0.000 title claims description 61
- 238000005260 corrosion Methods 0.000 title claims description 23
- 230000007797 corrosion Effects 0.000 title claims description 23
- 150000002739 metals Chemical class 0.000 title description 15
- 239000000243 solution Substances 0.000 claims description 54
- 239000011575 calcium Substances 0.000 claims description 50
- 239000011248 coating agent Substances 0.000 claims description 50
- 238000000576 coating method Methods 0.000 claims description 50
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 49
- 229910052791 calcium Inorganic materials 0.000 claims description 49
- 239000010953 base metal Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 18
- 239000011701 zinc Substances 0.000 claims description 18
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 16
- 229910052725 zinc Inorganic materials 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 12
- 229910045601 alloy Inorganic materials 0.000 claims description 10
- 239000000956 alloy Substances 0.000 claims description 10
- 229910052788 barium Inorganic materials 0.000 claims description 10
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052712 strontium Inorganic materials 0.000 claims description 10
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 10
- 229910052793 cadmium Inorganic materials 0.000 claims description 9
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
- 229910017052 cobalt Inorganic materials 0.000 claims description 8
- 239000010941 cobalt Substances 0.000 claims description 8
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 8
- 229910001463 metal phosphate Inorganic materials 0.000 claims description 8
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 6
- 239000010949 copper Substances 0.000 claims description 6
- 229910052802 copper Inorganic materials 0.000 claims description 6
- -1 FERROUS METALS Chemical class 0.000 claims description 5
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 34
- 239000005365 phosphate glass Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 230000001681 protective effect Effects 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 7
- ROPDWRCJTIRLTR-UHFFFAOYSA-L calcium metaphosphate Chemical compound [Ca+2].[O-]P(=O)=O.[O-]P(=O)=O ROPDWRCJTIRLTR-UHFFFAOYSA-L 0.000 description 7
- 239000001506 calcium phosphate Substances 0.000 description 7
- 229910000389 calcium phosphate Inorganic materials 0.000 description 7
- 235000011010 calcium phosphates Nutrition 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 7
- 229940108928 copper Drugs 0.000 description 5
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 150000002736 metal compounds Chemical class 0.000 description 4
- 235000019832 sodium triphosphate Nutrition 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000005341 metaphosphate group Chemical group 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 3
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 3
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 3
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 3
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000010962 carbon steel Substances 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 101100348017 Drosophila melanogaster Nazo gene Proteins 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
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- QUQFTIVBFKLPCL-UHFFFAOYSA-L copper;2-amino-3-[(2-amino-2-carboxylatoethyl)disulfanyl]propanoate Chemical compound [Cu+2].[O-]C(=O)C(N)CSSCC(N)C([O-])=O QUQFTIVBFKLPCL-UHFFFAOYSA-L 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 235000021110 pickles Nutrition 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001467 sodium calcium phosphate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- UGTZMIPZNRIWHX-UHFFFAOYSA-K sodium trimetaphosphate Chemical compound [Na+].[Na+].[Na+].[O-]P1(=O)OP([O-])(=O)OP([O-])(=O)O1 UGTZMIPZNRIWHX-UHFFFAOYSA-K 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000002699 waste material Substances 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
- C23C22/05—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
- C23C22/68—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 solutions with pH between 6 and 8
-
- 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
- C23C22/23—Condensed phosphates
Definitions
- This invention relates to a process of making metallic articles corrosion-resistant by depositing on the article from an aqueous solution an amorphous film or coating formed by the interaction of one or more coating metal ions with one or more molecularly dehydrated phosphate radicals, the solution being of such character that the film is deposited without visible attack on the surface of the article.
- the amorphous films characteristic of my invention are substantially even in thickness, continuous and flexible as contrasted with the hard granular crystalline deposits obtained from orthophosphoric acid metal-treating solutions. They are superior to the crystalline deposits, particularly for those uses where the metal is first treated to improve its corrosion-resistance and then is formed to shape, as by bending or drawing, since the flexible amorphous films have less tendency to crack when bent or drawn.
- the invention is applicable to preventing or retarding corrosion of the steel sheet by the atmosphere, irrespective of the particular use to which the steel is to be put; but the above have been given merely by way of example of certain applications of the invention.
- the invention will be described as applied to improving the corrosion-resistance of steel sheets, it being understood that other metals or their alloys may be treated according to my process to improve their resistance to corrosion.
- the steel sheet is first cleaned by any suitable method and is then treated with an aqueous solution which forms an amorphous protective film orcoating on the sheet.
- the aqueous treating solution may be applied to the sheet by any suitable method, for example, immersion of the sheet in the treating solution or by spraying the treating solution on the sheet.
- the treating solu- 2 tion is of such character that there is formed on the sheet an amorphous protective film of material produced by the interaction of one or more molecularly dehydrated phosphate radicals and one or more coating metals of the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt and manganese.
- the calcium metaphosphate film is formed on the sheet by providing in the treating solution calcium ion and metaphosphate radical in the proper concentrations and ratios and treating the sheet with the solution under the proper conditions of pH and temperature all as will be explained more fully hereinafter.
- the desired amorphous protective film of calcium metaphosphate for example, there must be a sufflcient concentration of calcium and 01' metaphosphate radical to form the film by subjecting the sheet to the treating solution for a reasonable period of time.
- the weight ratio of metaphosphate to calcium must be within certain limits. If the ratio of metaphosphate to calcium is too low, the solution does not provide sufiicient metaphosphate radical for uniting with the calcium to form the protective film of calcium metaphosphate. On the other hand, if the ratio of metaphosphate to calcium is too high, the effect is to prevent the formation of the calcium metaphosphate film.
- the minimum efiective concentration of calcium is about 100 P. P. M. (parts per million by weight).
- the amount of sodium phosphate glass having a molar ratio of NazO to P205 of 1.1:1, often referred to as technical grade Graham's salt or sodium hexametaphosphate should be in the range of about 200 to 1000 P. P. M. but preferably about 500 P. P. M.
- this sodium phosphate glass contains about 67% P205, this means that the P205 content, said P20 5 being derived from the aforementioned sodium phosphate glass, should amount to about 134-670 P. P. M.
- the pH value of this particular treating solution should be in the range of 4.120 '7, preferably about pH 5.
- the treatment may be given by immersion of clean ferrous metal in the solution for ten minutes at room temperature.
- the optimum weight ratio of this phosphate glass to calcium in the stated concentration of 100 P. P. M. is about 5:1, the optimum weight ratio of the P205 to calcium being about 3.4:1.
- the effective weight ratio of this phosphate glass to calcium is about 2:1 to :1.
- the range of effective ratios of this phosphate glass to calcium is widened downwardly, so that a con centration of 5000 P. P. M. calcium the'eflective weight ratio of this phosphate glass to calcium is between about 0.05:1 and 10:1, which means a weight ratio of P205 to calcium between about 0.03:1 and 7:1.
- a steel sheet was treated in a solution having a pH of 5 for one minute at 65 C., the solution containing '300 P. P. M. calcium and 1500 P. P. M. phosphate glass having a molar ratio of Na2O to P205 of 1.1:1.
- the sheet was then rinsed with water and allowed to dry at room temperature. No rust spots could be found on this sheet after drying, while an untreated sheet similarly rinsed with water and allowed to dry at room temperature showed many rust spots.
- a one-minute exposure at 65 C is roughly equivalent to 10 minutes exposure at room temperature.
- an amorphous film can be produced in less than one minute, but since high temperature causes decomposition of the phosphate glass, the use of such high temperature is uneconomical.
- the invention has been described thus far principally in connection with the formation of a film of calcium metaphosphate.
- other coating metals may be substituted in whole or in part for the calcium, and other molecularly dehydrated phosphate radicals, for example, tripolyphosphate radical P3010 or pyrophosphate radical P207 may be substituted in whole or in part for the metaphosphate radical P05.
- I may use as coating metals strontium, barium, zinc, cadmium, nickel, co-
- balt and manganese All of these coating metals have the common. property of reacting in solution with molecularly dehydrated phosphate radicals when in proper concentrations and ratios and at proper pH values to form amorphous protective films on base metals without visible attack on the base metal.
- the nature of the anions in compounds of the coating metals does not appear to be critical.
- any compound of these metals can be used which provides one or more of the coating metals in solution in the treating bath. I may, for example, use the soluble chlorides, sulphates, acetates, chromates, nitrates or hydroxides of the metals for supplying the metal ions to the solution.
- Certain compounds of the metals are especially eiiective due to their pH value or neutralizing or bufier value.
- calcium chloride is a ver effective compound for use with a phosphate glass having a molar ratio of 113.20 to P205 of 1.1:1, because the pH values of aqueous solutions containing effective amounts of calcium chloride and such phosphate glass are about 5, which has been found to be the optimum pH value of the treating solution when the solution contains about -300 P. P. M of calcium]
- desirable coating metal compounds are the carbonates or hydroxides. Such compounds not only supply part or all of the necessary coating metal which is to react with the molecularly dehydrated phosphate radical to form the protective film but act as neutralizing agents as Well.
- molecularly dehydrated phospha any phosphate or phosphoric acid which can be considered as derived from monobasic or dibasic orthophosphate or orthophosphoric acid or mixtures thereof by removal of water of constitution. Included in this term are the sodium phosphate glass commonly referred to as technical grade Graham's salt, which has a.
- the preferred molecularly dehydrated phosphates for use according to the invention are the glasses which extend from P205 at the acid end of the materials through the phosphate glasses made by rapidly chilling a melt of the proper composition including the acid phosphate glasses, the neutral phosphate glasses and the alkaline phosphate glasses up to a composition at the alkaline end of the range of materials in the vicinity of sodium tripolyphosphate Na5Pz0m, which has a molar ratio of Na2O to P205 of 5:3.
- the sodium phosphate glass with a molar ratio of Na2O to P205 of 5:3 is more eflective than crystalline sodium tripolyphosphate NasPsOm.
- column 1 shows the molecularly dehydrated phosphate used in the treating solution.
- Column 2 shows the molar ratio of No.20 :P205 of the molecuiarly dehydrated phosphate.
- Column 3 shows the concentration in parts per million or the molecularly dehydrated phosphate.
- Column 4 shows the coating metal compound employed in the treating solution and column 5 the concentration in parts per million of the coating metal.
- Column 6 shows the weight ratio of P205 content of the molecularly dehydrated phosphate to the coating metalemployed.
- Column 7 shows the pH value of the treating solution and columns 8 and 9'show respectively the temperature of the treatment of mild car on .steel.
- a 'pH of 3 can the concentration of the coating metal
- the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating the effective range of this ratio for each of the re i u n d the t e of atm nt in employed in the treating solution, the concentration of the 15 molecularly dehydrated phosphate in the treating solution and the P20: content or the molecularly dehydrated phosphate.
- lower 'pI-I values can be employed with higher concentrations of coating metal.
- the pH should be 4 or higher.
- the pH of the solution should not be above about 8 or 9 because with a higher pH than this no substantial amount of coating is formed. In general, the pH should not be above 7 and I prefer to employ a pH of about 4 or 5.
- I may dissolve a material containing both coating metal and molecularly dehydrated phosphate radical in water. I may, for example, form the treating solution by dissolving a calcium phosphate glass in water or I may maintain the strength of the treating solution by adding calcium phosphate glass to a bath previously formed by dissolving a calcium compound and a sodium phosphate glass in water.
- the calcium phosphate glass is quite slowly soluble and this is advantageous because it provides an efiectlve means for continuously supplying calcimn and molecularly dehydrated phosphate to replace that which is removed in the formation of the film on the metal being treated to render it corrosion resistant.
- a glass with a molar ratio of CaO to P205 of 1:1, corresponding to calcium metaphosphate is dissolved in water, it provides molecularly dehydrated phosphate radical and calcium in substantially the optimum ratio for preventing corrosion.
- I may use a sodium calcium phosphate glass, for example, that having the formula and the pH values of the treatin solution are preferably maintained within the ranges given in connection with the formation of the treating solution by the separate use of calcium or other metal compound and molecularly dehydrated phosphate not containing coating met/a1.
- Any of the molecularly dehydrated phosphates may contain potassium or ammonium in place of sodium whether they do or do not contain coating metal.
- the following method is one which may be employed in forming the corrosion resistant amorphous film on a mild carbon steel strip.
- the strip is cleaned with an alkaline detergent, followed by a 15-second pickle in 5 to 10% sulphuric acid.
- the pickling is not an essential step and it is to be understood that any method which provides a clean grease-free surface is a satisfactory preparation of the metal for the corrosion resisting treatment.
- the strip is immersed in the treating solution at a temperature and for a time dependent upon the particular corrosion conditions to which the strip is to be subjected. Where the treating solution contains 300 P. P. M. calcium, 1500 P. P. M. phosphate glass having a molar ratio of Na20 to P205 of 1.1:1 and has a pH of 5, the strip may be immersed in-the solution maintained at a temperature of about 65 C.
- the strip may be allowed to dry without rinsing or it may be rinsed incold or hot water.
- Such treatment provides an amorphous film on the strip which renders the strip corrosion-resistant when exposed to air during the time and under conditions normally encoun-' tered between the end of the rolling of the strip and the time that it is given an enamellin or lithographing treatment.
- Zinc, and their alloys for improving ther resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially greasefree an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being'present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially amorphous film thereover, the film being characterized by a good quality
- the process of treating ferrous metal articles for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality
- the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7: 1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
- the process of treating articles of zinc and its alloys for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of calcium, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the calcium being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous calcium phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
- the process of treating base metal articles of the group consisting of ferrous metals, copper, zinc, and their alloys, for improving their resistance to atmospheric corrosion which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt and manganese, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7:1, the pH value-of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the article so as to provide a dry exterior surface having a substantially continuous amorphous film thereover.
- at least one coating metal selected from the group consisting of calcium, stront
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Description
Patented Nov. 7, 1950 UNITED STATES PATENT OFFICE PROTECTION OF METALS FROM CORROSION No Drawing. Application September 8, 1947, Serial No. 772,894
10 Claims. 1
This invention relates to a process of making metallic articles corrosion-resistant by depositing on the article from an aqueous solution an amorphous film or coating formed by the interaction of one or more coating metal ions with one or more molecularly dehydrated phosphate radicals, the solution being of such character that the film is deposited without visible attack on the surface of the article. The amorphous films characteristic of my invention are substantially even in thickness, continuous and flexible as contrasted with the hard granular crystalline deposits obtained from orthophosphoric acid metal-treating solutions. They are superior to the crystalline deposits, particularly for those uses where the metal is first treated to improve its corrosion-resistance and then is formed to shape, as by bending or drawing, since the flexible amorphous films have less tendency to crack when bent or drawn.
This application is a continuation-in-part of process whereby mild carbon steel sheets can be :7
protected from corrosion by the atmosphere during the period of time after the rolling is completed until the sheet is subjected to a further treatment such as lithographing, in case the sheet is to be made into containers or until enamelling, in case it is to be enamelled. The invention is applicable to preventing or retarding corrosion of the steel sheet by the atmosphere, irrespective of the particular use to which the steel is to be put; but the above have been given merely by way of example of certain applications of the invention.
The invention will be described as applied to improving the corrosion-resistance of steel sheets, it being understood that other metals or their alloys may be treated according to my process to improve their resistance to corrosion.
The steel sheet is first cleaned by any suitable method and is then treated with an aqueous solution which forms an amorphous protective film orcoating on the sheet. The aqueous treating solution may be applied to the sheet by any suitable method, for example, immersion of the sheet in the treating solution or by spraying the treating solution on the sheet. The treating solu- 2 tion is of such character that there is formed on the sheet an amorphous protective film of material produced by the interaction of one or more molecularly dehydrated phosphate radicals and one or more coating metals of the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt and manganese. As an example of the material which can be deposited to form the amorphous protective coating, I mention calcium metaphosphate Ca(POa) 2. The calcium metaphosphate film is formed on the sheet by providing in the treating solution calcium ion and metaphosphate radical in the proper concentrations and ratios and treating the sheet with the solution under the proper conditions of pH and temperature all as will be explained more fully hereinafter.
In order to form the desired amorphous protective film of calcium metaphosphate, for example, there must be a sufflcient concentration of calcium and 01' metaphosphate radical to form the film by subjecting the sheet to the treating solution for a reasonable period of time. Also the weight ratio of metaphosphate to calcium must be within certain limits. If the ratio of metaphosphate to calcium is too low, the solution does not provide sufiicient metaphosphate radical for uniting with the calcium to form the protective film of calcium metaphosphate. On the other hand, if the ratio of metaphosphate to calcium is too high, the effect is to prevent the formation of the calcium metaphosphate film.
For purposes of practical short-time treatment of iron and steel, to render them corrosion-resistant when they are exposed to the atmosphere for relatively short periods of time, the minimum efiective concentration of calcium is about 100 P. P. M. (parts per million by weight). For a calcium concentration of 100 P. P. M., the amount of sodium phosphate glass having a molar ratio of NazO to P205 of 1.1:1, often referred to as technical grade Graham's salt or sodium hexametaphosphate, should be in the range of about 200 to 1000 P. P. M. but preferably about 500 P. P. M. Since this sodium phosphate glass contains about 67% P205, this means that the P205 content, said P20 5 being derived from the aforementioned sodium phosphate glass, should amount to about 134-670 P. P. M. The pH value of this particular treating solution should be in the range of 4.120 '7, preferably about pH 5. The treatment may be given by immersion of clean ferrous metal in the solution for ten minutes at room temperature.
0 or one minute at 65 C. The optimum weight ratio of this phosphate glass to calcium in the stated concentration of 100 P. P. M. is about 5:1, the optimum weight ratio of the P205 to calcium being about 3.4:1. In the case-of low concentrations such as 100 P. P. M. of calcium, the effective weight ratio of this phosphate glass to calcium is about 2:1 to :1. However, as the calcium concentration level is increased, the range of effective ratios of this phosphate glass to calcium is widened downwardly, so that a con centration of 5000 P. P. M. calcium the'eflective weight ratio of this phosphate glass to calcium is between about 0.05:1 and 10:1, which means a weight ratio of P205 to calcium between about 0.03:1 and 7:1. Thus there appears to be a minimum effective concentration of this phosphate glass at about 200 P. P. M. whereas the maximum effective concentration bears a constant relation to the calcium concentration, 1. e., about 10:1. The 5:1 ratio of this phosphate glass to calcium is the optimum ratio and gives satisfactory results over the whole range or calcium concentrations from 100 P. P. M. up to 5000 P. P. M. or even higher.
There appears to be no real upper limit to the concentrations 01. calcium and phosphate glass in solution so long as the proper ratio between them is maintained. However, due to the bulk of undissolved or precipitated material present, it probably is neither practical nor economical to operate above the 1000 P. P. M. calcium level if the pH of the solution is 5 or above. Since the amount of calcium which can be held in solution in a solution having a pH of 5 is around 300 P. P. M. calcium at room temperature and is lower at elevated temperatures, the optimum concentration of calcium in a solution having this pH value appears to be about 300 P. P. M. Lower concentrations than this are spent more rapidly whereas higher concentrations lead to waste of treating material. However, higher concentrations of calcium can be employed if the v pH of the solution is lowered.
In one example of the process, a steel sheet was treated in a solution having a pH of 5 for one minute at 65 C., the solution containing '300 P. P. M. calcium and 1500 P. P. M. phosphate glass having a molar ratio of Na2O to P205 of 1.1:1. The sheet was then rinsed with water and allowed to dry at room temperature. No rust spots could be found on this sheet after drying, while an untreated sheet similarly rinsed with water and allowed to dry at room temperature showed many rust spots.
Within practical limits, the higher the temperature and the longer the time of exposure to the solution, themore effective the treatment becomes. A one-minute exposure at 65 C, is roughly equivalent to 10 minutes exposure at room temperature. At 100 C., an amorphous film can be produced in less than one minute, but since high temperature causes decomposition of the phosphate glass, the use of such high temperature is uneconomical.
The invention has been described thus far principally in connection with the formation of a film of calcium metaphosphate. However, other coating metals may be substituted in whole or in part for the calcium, and other molecularly dehydrated phosphate radicals, for example, tripolyphosphate radical P3010 or pyrophosphate radical P207 may be substituted in whole or in part for the metaphosphate radical P05.
In place of calcium, I may use as coating metals strontium, barium, zinc, cadmium, nickel, co-
balt and manganese. All of these coating metals have the common. property of reacting in solution with molecularly dehydrated phosphate radicals when in proper concentrations and ratios and at proper pH values to form amorphous protective films on base metals without visible attack on the base metal. The nature of the anions in compounds of the coating metals does not appear to be critical. Apparently any compound of these metals can be used which provides one or more of the coating metals in solution in the treating bath. I may, for example, use the soluble chlorides, sulphates, acetates, chromates, nitrates or hydroxides of the metals for supplying the metal ions to the solution. Certain compounds of the metals are especially eiiective due to their pH value or neutralizing or bufier value. For example, calcium chloride is a ver effective compound for use with a phosphate glass having a molar ratio of 113.20 to P205 of 1.1:1, because the pH values of aqueous solutions containing effective amounts of calcium chloride and such phosphate glass are about 5, which has been found to be the optimum pH value of the treating solution when the solution contains about -300 P. P. M of calcium] If a. more acid phosphate glass, for example, one having a ratio of Na2O to P205 of 0.7:1 is employed in the treating solution, desirable coating metal compounds are the carbonates or hydroxides. Such compounds not only supply part or all of the necessary coating metal which is to react with the molecularly dehydrated phosphate radical to form the protective film but act as neutralizing agents as Well.
The whole range of molecularly dehydrated phosphates, starting with tetrasodium pyrophosphate and extending to metaphosphoric acid (fresh P205 solution) appears to be efiective in forming the protective fiim when the pH value is adjusted to the proper level. By molecularly dehydrated phospha is meant any phosphate or phosphoric acid which can be considered as derived from monobasic or dibasic orthophosphate or orthophosphoric acid or mixtures thereof by removal of water of constitution. Included in this term are the sodium phosphate glass commonly referred to as technical grade Graham's salt, which has a. molar ratio of Na2O to P205 of 1.1:1, pentasodium tripolyphosphate Na5Pa0m, which has a molar ratio of Na2O to P205 of 5:3, and tetrasodium pyrophosphate Na4P20'1 having a molar ratio of Na2O to P205 of 2:1. These are given merely by way ofexample, as illustrating the more common alkali-metal molecularly dehydrated phosphates which are either substantially neutral or alkaline in reaction. The preferred molecularly dehydrated phosphates for use according to the invention are the glasses which extend from P205 at the acid end of the materials through the phosphate glasses made by rapidly chilling a melt of the proper composition including the acid phosphate glasses, the neutral phosphate glasses and the alkaline phosphate glasses up to a composition at the alkaline end of the range of materials in the vicinity of sodium tripolyphosphate Na5Pz0m, which has a molar ratio of Na2O to P205 of 5:3. The sodium phosphate glass with a molar ratio of Na2O to P205 of 5:3 is more eflective than crystalline sodium tripolyphosphate NasPsOm. Acid sodium phosphate glass with a molar ratio of Na2O to P205 of 0.87:1 (pH 2.8) and freshly dissolved P205 both give good results when the pH value of the solution is adjusted to the proper level, The water soluble crystalline pentasodium tripoly- R eoi Raios Time of Minutes 45007147 &LLL 0 L0 Treatment,
. l 5 5 5 1 0010 mmm mmwmmm mmmww mm mm m an a m mm 1 In this table Coating Metal womb ho; content of moleculariy dehydrated phosphate Metal phosphate and the tetrasodium pyrophosphate and sodium trimetaphosphate are not nearly as eflective in producing the amorphous protective film as are the glassy molecularly dehydrated phosphates. 5
As has been pointed out previously herein, where calcium is employed as the coating metal and is used in the minimum concentration of about 100 P. P. M., the optimum pH value of the Caicium. Strontium.
Barium.
7lnr' Cadmium-- solution is about 5 and the eiiective pH range is from 4 to "I. The optimum pH value of the solution, according to my invention, will vary depending upon such factors as the coating metal tlon Treating SolupH Temp,
000005000000000000000000000022555557000000 5 mewiflxmdifii a wixwixmd mi w wiizwzwomamswla momiamoaiti.azmG-L Weight Ratio-- P105 in Phosphate: Coating Metal wwwmwmmwmommmwmmnmmmmmmwmamwwmawmammmmmufim Table H which follows, gives numerous .ex-
mmaanaamaammmmmmmmmmaaaaamwaammmmmmam amples embodying widely varying conditions under which my process can be carried out in the column 1 shows the molecularly dehydrated phosphate used in the treating solution. Column 2 shows the molar ratio of No.20 :P205 of the molecuiarly dehydrated phosphate. Column 3 shows the concentration in parts per million or the molecularly dehydrated phosphate. Column 4 shows the coating metal compound employed in the treating solution and column 5 the concentration in parts per million of the coating metal. Column 6 shows the weight ratio of P205 content of the molecularly dehydrated phosphate to the coating metalemployed. Column 7 shows the pH value of the treating solution and columns 8 and 9'show respectively the temperature of the treatment of mild car on .steel.
minutes.
Table II Thus, a 'pH of 3 can the concentration of the coating metal The weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating the effective range of this ratio for each of the re i u n d the t e of atm nt in employed in the treating solution, the concentration of the 15 molecularly dehydrated phosphate in the treating solution and the P20: content or the molecularly dehydrated phosphate. In general, lower 'pI-I values can be employed with higher concentrations of coating metal.
be used if the calcium concentration is, say, 1500 P. P. M. or higher, whereas if the calcium concentration is of the order of 300 P. P. M. or lower, the pH should be 4 or higher. The pH of the solution should not be above about 8 or 9 because with a higher pH than this no substantial amount of coating is formed. In general, the pH should not be above 7 and I prefer to employ a pH of about 4 or 5.
metal varies over a fairly wide range for some coating metals and over a narrower range for other coating metals. The optimum ratio and coating metals is given in Table I.
Table IL-Continued Molwularly Ddiydntad Phoqxhato Coating Metal 1 115 11 We ht Ratio- No. P, 1 in Phos- .333;; Concentra- Couoentrafizg Tam Minutes Compound Nico tion. Compound tion, pH s P. r. M. P. P. M. P1):
Sodium Phosphate o1m 1. 1 1, 500 Zn(N01)a- 5, 000 1. 01 a. 40
44 do 1.1 4,500 m 5,500 0.55 3.5 48
45 an 1.1 4,500 m 5,500 0.55 4.0 48 10 45 do 1. 1 4, 500 n 5,500 0. 55 5. 0 4s 10 1. 1 3, 150 Z1150 a, 150 0. 0s 5. 0 49 10 1. 1 500 Zn 500 0. 5s 5. 0 10 1. 1 2, 500 500 a. as 5. 0 25 10 1. 1 1,500 5, 000 1. 00 4. 0 4s 10 1. 1 1, 500 a, 300 1. s0 3. 0 4s 10 1. 1 1, 500 a, 300 1. s0 4. 5 4s 10 1. 1 500 1, 000 0. a4 5 0 25 10 1.1 2,000 0...--. 1,000 1.35 5.0 25 10 1. 1 21s N1so1. 2, 222 0. 0a 4. 0 10 1. 1 21a 0.- 2, 222 0. 0s 5. 0 40 10 1.1 ,250 do 1,250 0.58 5.0 49 10 1. 1 500 500 0. 5a 5. 0 25 10 1. 1 500 a. as 5. 0 25 10 1. 1 500 2. 0a 5. 0 1 1. 1 500 2. 0a 4. 0 25 10 1. 1 500 2. 0a 5. 0 25 10 1. 1 500 2. 03 5. 0 25 10 l. 1 500 2. 03 1. 0 25 10 1. 1 500 0. 5s 5. 0 25 10 1. 1 500 3. 3s 5. 0 25 10 1. 1 250 0. 5s 5. 0 25 10 1. 1 250 2. 03 5. 0 25 10 1. 1 00-- 250 3.38 5. 0 25 10 1.1 500 M11801 4, 500 0.68 2. 5 4s 10 1.1 4,500 -d 4,500 0. 0a 4.0 48 10 1. 1 500 do 8,200 0. 01 4. 0 4s 10 1. 1 800 do 8,200 0. 01 5. 0 4s 10 1. 1 4, 500 do 4, 500 0. 5s 5. 0 4s 10 1. 1 1,500 -do 1,500 2. 31 5. 0 4s 10 Instead of making up the treating solution by dissolving a coating metal compound and a molecularly dehydrated phosphate in water, I may dissolve a material containing both coating metal and molecularly dehydrated phosphate radical in water. I may, for example, form the treating solution by dissolving a calcium phosphate glass in water or I may maintain the strength of the treating solution by adding calcium phosphate glass to a bath previously formed by dissolving a calcium compound and a sodium phosphate glass in water. The calcium phosphate glass is quite slowly soluble and this is advantageous because it provides an efiectlve means for continuously supplying calcimn and molecularly dehydrated phosphate to replace that which is removed in the formation of the film on the metal being treated to render it corrosion resistant. When a glass with a molar ratio of CaO to P205 of 1:1, corresponding to calcium metaphosphate, is dissolved in water, it provides molecularly dehydrated phosphate radical and calcium in substantially the optimum ratio for preventing corrosion.
I may use a sodium calcium phosphate glass, for example, that having the formula and the pH values of the treatin solution are preferably maintained within the ranges given in connection with the formation of the treating solution by the separate use of calcium or other metal compound and molecularly dehydrated phosphate not containing coating met/a1.
Any of the molecularly dehydrated phosphates may contain potassium or ammonium in place of sodium whether they do or do not contain coating metal.
The following method is one which may be employed in forming the corrosion resistant amorphous film on a mild carbon steel strip. The strip is cleaned with an alkaline detergent, followed by a 15-second pickle in 5 to 10% sulphuric acid. The pickling is not an essential step and it is to be understood that any method which provides a clean grease-free surface is a satisfactory preparation of the metal for the corrosion resisting treatment. The strip is immersed in the treating solution at a temperature and for a time dependent upon the particular corrosion conditions to which the strip is to be subjected. Where the treating solution contains 300 P. P. M. calcium, 1500 P. P. M. phosphate glass having a molar ratio of Na20 to P205 of 1.1:1 and has a pH of 5, the strip may be immersed in-the solution maintained at a temperature of about 65 C.
for a period of the order of one minute. After this treatment, the strip may be allowed to dry without rinsing or it may be rinsed incold or hot water. Such treatment provides an amorphous film on the strip which renders the strip corrosion-resistant when exposed to air during the time and under conditions normally encoun-' tered between the end of the rolling of the strip and the time that it is given an enamellin or lithographing treatment.
The invention is not limited to the preferred materials or practice, which have been given merely for illustrative purposes, but may be' otherwise embodied or practiced within the scope of the following claims.
1. The process of treating base metal articles of the group consisting of ferrous metals, copper,
Zinc, and their alloys, for improving ther resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially greasefree an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being'present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially amorphous film thereover, the film being characterized by a good quality,of bondability with nonferrous finishes.
2. The process of treating base metal articles of the group consisting of ferrous metals, cop per, zinc, and their alloys for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of calcium, the metal being present in the form of a water-soluble salt, and at least one'molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the calcium being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous calcium phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
3. The process of treating ferrous metal articles for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
3 and 9 and such that an amorphous calcium phosphate film is deposited on the base metal, without visible attack on the base metal surface,
and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
5. The process of treating articles of zinc and its alloys for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of at least one coating metal selected from the group consisting of calcium, strontium,
barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7: 1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
6. The process of treating articles of zinc and its alloys for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of calcium, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the calcium being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous calcium phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
7. The process of treating articles of copper and its alloys for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the 4- Th Process f reating ferrous metal articles articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being present in the form of a water-solublesalt, and at least one molecularly dehydrated phosphate, the weight ratio of P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03: 1 and '7 1 the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and
thereafter drying the articles so as to provide a dry finish-receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
8. The process of treating articles of copper and its alloys for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts per million by weight of calcium, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the calcium being between 0.03 1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous calcium phosphate film is deposited on the base metal without visible attack on the basemetal surface, and thereafter drying the articles so as to provide a dry finish receptive exterior surface having a substantially continuous amorphous film thereover, the film being characterized by a good quality of bondability with nonferrous finishes.
9. The process of treating base metal articles of the group consisting of ferrous metals, copper, zinc, and their alloys, for improving their resistance to atmospheric corrosion, preparatory to applying a nonferrous finish which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one hundred parts l2 per million by weight of at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt, and manganese, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate glass, the weight ratio of the P205 content of the molecularly dehydrated phosphate glass to the coating metal being between 0.03:1 and 7:1, the pH value of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the articles-so as to provide a dry finish-receptive exterior surface having a substantially amorphous film thereover, the film being characterized by a good quality of bondability with non-ferrous finishes.
10. The process of treating base metal articles of the group consisting of ferrous metals, copper, zinc, and their alloys, for improving their resistance to atmospheric corrosion, which comprises treating the articles to render substantially grease-free an exterior surface to be protected, applying to the grease-free surface an aqueous solution containing at least one coating metal selected from the group consisting of calcium, strontium, barium, zinc, cadmium, nickel, cobalt and manganese, the metal being present in the form of a water-soluble salt, and at least one molecularly dehydrated phosphate, the weight ratio of the P205 content of the molecularly dehydrated phosphate to the coating metal being between 0.03:1 and 7:1, the pH value-of the solution being between 3 and 9 and such that an amorphous coating metal phosphate film is deposited on the base metal without visible attack on the base metal surface, and thereafter drying the article so as to provide a dry exterior surface having a substantially continuous amorphous film thereover.
CHARLES T. ROLAND.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS
Claims (1)
1. THE PROCESS OF TREATING BASE METAL ARTICLES OF THE GROUP CONSISTING OF FERROUS METALS, COPPER, ZINC, AND THEIR ALLOYS, FOR IMPROVING THEIR RESISTANCE TO ATMOSPHERIC CORROSION, PREPARATORY TO APPLYING A NONFERROUS FINISH WHICH COMPRISES TREATING THE ARTICLES TO RENDER SUBSTANTIALLY GREASEFREE AN EXTERIOR SURFACE TO BE PROTECTED, APPLYING TO THE GREASE-FREE SURFACE AN AQUEOUS SOLUTION CONTAINING AT LEAST ONE HUNDRED PARTS PER MILLION BY WEIGHT OF AT LEAST ONE COATING METAL SELECTED FROM THR GROUP CONSISTING OF CALCIUM, STRONTIUM, BARIUM, ZINC, CADMIUM, NICKEL, COBALT, AND MANGANESE, THE METAL BEING PRESENT IN THE FORM OF A WATER-SOLUBLE SALT, AND AT LEAST ONE MOLEUCULARLY DEHYDRATED PHOSPHATE, THE WEIGHT RATIO OF THE P2O5 CONTENT OF THE MOLECULARLY DEHYDRATED PHOSPHATE TO THE COATING METAL BEING BETWEEN 0.03:1 AND 7:1, THE PH VALUE OF THE SOLUTION BEING BETWEEN 3 AND 9 AND SUCH THAT AN AMORPHOUS COATING METAL PHOSPHATE FILM IS DEPOSITED ON THE BASE METAL WITHOUT VISIBLE ATTACK ON THE BASE METAL SURFACE, AND THEREAFTER DRYING THE ARTICLES SO AS TO PROVIDE A DRY FINISH-RECEPTIVE EXTERIOR SURFACE HAVING A SUBSTANTIALLY AMORPHOUS FILM THEREOVER, THE FILM BEING CHARACTERIZED BY A GOOD QUALITY OF BONDABILITY WITH NONFERROUS FINISHES.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US772894A US2528787A (en) | 1947-09-08 | 1947-09-08 | Protection of metals from corrosion |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US772894A US2528787A (en) | 1947-09-08 | 1947-09-08 | Protection of metals from corrosion |
Publications (1)
Publication Number | Publication Date |
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US2528787A true US2528787A (en) | 1950-11-07 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US772894A Expired - Lifetime US2528787A (en) | 1947-09-08 | 1947-09-08 | Protection of metals from corrosion |
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US (1) | US2528787A (en) |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2715059A (en) * | 1951-08-06 | 1955-08-09 | Kelite Products Inc | Phosphatizing composition |
US2758949A (en) * | 1951-06-28 | 1956-08-14 | Parker Rust Proof Co | Alkali metal phosphate coating solutions and the method of forming coatings therewith |
US2874081A (en) * | 1956-08-02 | 1959-02-17 | Parker Rust Proof Co | Pretreatment solution for phosphate coating, method of preparing the same and process of treating metal surfaces |
DE1057846B (en) * | 1954-09-02 | 1959-05-21 | Metallgesellschaft Ag | Process for the production of coatings from alkaline earth phosphate |
DE973195C (en) * | 1951-01-18 | 1959-12-17 | Metallgesellschaft Ag | Process for coating metal surfaces with a phosphate layer |
US2930723A (en) * | 1954-12-07 | 1960-03-29 | Walterisation Company Ltd | Surface treatment of metals |
US2935423A (en) * | 1956-09-25 | 1960-05-03 | William H Kapfer | Process for applying a protective coating to a magnesium surface |
US2939809A (en) * | 1956-12-07 | 1960-06-07 | Douglas Aircraft Co Inc | Dry film lubrication |
DE1090048B (en) * | 1955-02-02 | 1960-09-29 | Metallgesellschaft Ag | Process for the preparation of metallic workpieces for cold forming |
US2975082A (en) * | 1957-01-22 | 1961-03-14 | John A Henricks | Method of providing ferrous articles with phosphate coatings and compositions therefor |
US2980553A (en) * | 1958-06-23 | 1961-04-18 | Smith Corp A O | Glass coated steel article and method of making the same |
US2984592A (en) * | 1958-03-19 | 1961-05-16 | Chem Metals Inc | Protective coatings for galvanized members |
DE1111480B (en) * | 1956-01-07 | 1961-07-20 | Metallgesellschaft Ag | Process to facilitate the cold deformation of heat-treated iron or steel workpieces |
US3015593A (en) * | 1960-10-04 | 1962-01-02 | Jayne John Phillip | Methods and composition for producing a phosphate coating on zinc metal |
US3152018A (en) * | 1961-11-01 | 1964-10-06 | Wyandotte Chemicals Corp | Room temperature phosphate coating composition |
DE1192489B (en) * | 1951-11-19 | 1965-05-06 | Metallgesellschaft Ag | Phosphating process |
US3218200A (en) * | 1953-08-10 | 1965-11-16 | Lubrizol Corp | Phosphate coating of metals |
US3904346A (en) * | 1971-12-23 | 1975-09-09 | Leslie Earl Shaw | Electrostatic powder coating process |
FR2492413A1 (en) * | 1980-10-22 | 1982-04-23 | Chaffoteaux Et Maury | Pyrophosphate conversion coating of zinc surface - using pyrophosphate- and nitrate-contg. soln. of controlled pH |
FR2531457A1 (en) * | 1982-08-03 | 1984-02-10 | Roquette Freres | SOLUTION AND PROCESS FOR THE CHEMICAL CONVERSION OF METAL SUBSTRATES |
EP0946786A1 (en) * | 1996-11-27 | 1999-10-06 | Henkel Corporation | Aqueous composition and process for preparing metal substrate for cold forming |
US20150340138A1 (en) * | 2009-02-24 | 2015-11-26 | Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) | Iron-based soft magnetic powder for dust core, method for manufacturing the same, and dust core |
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US2299748A (en) * | 1939-05-13 | 1942-10-27 | Hall Lab Inc | Control of calcium carbonate deposition for corrosion inhibition |
US2337856A (en) * | 1942-10-27 | 1943-12-28 | Hall Lab Inc | Process of retarding the corrosion of metal by water |
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1947
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US2299748A (en) * | 1939-05-13 | 1942-10-27 | Hall Lab Inc | Control of calcium carbonate deposition for corrosion inhibition |
US2337856A (en) * | 1942-10-27 | 1943-12-28 | Hall Lab Inc | Process of retarding the corrosion of metal by water |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE973195C (en) * | 1951-01-18 | 1959-12-17 | Metallgesellschaft Ag | Process for coating metal surfaces with a phosphate layer |
US2758949A (en) * | 1951-06-28 | 1956-08-14 | Parker Rust Proof Co | Alkali metal phosphate coating solutions and the method of forming coatings therewith |
DE970846C (en) * | 1951-06-28 | 1958-11-06 | Metallgesellschaft Ag | Process to prevent sludge formation in phosphating baths with non-layer-forming metal ions |
US2715059A (en) * | 1951-08-06 | 1955-08-09 | Kelite Products Inc | Phosphatizing composition |
DE1192489B (en) * | 1951-11-19 | 1965-05-06 | Metallgesellschaft Ag | Phosphating process |
US3218200A (en) * | 1953-08-10 | 1965-11-16 | Lubrizol Corp | Phosphate coating of metals |
DE1057846B (en) * | 1954-09-02 | 1959-05-21 | Metallgesellschaft Ag | Process for the production of coatings from alkaline earth phosphate |
US2930723A (en) * | 1954-12-07 | 1960-03-29 | Walterisation Company Ltd | Surface treatment of metals |
DE1090048B (en) * | 1955-02-02 | 1960-09-29 | Metallgesellschaft Ag | Process for the preparation of metallic workpieces for cold forming |
DE1111480B (en) * | 1956-01-07 | 1961-07-20 | Metallgesellschaft Ag | Process to facilitate the cold deformation of heat-treated iron or steel workpieces |
US2874081A (en) * | 1956-08-02 | 1959-02-17 | Parker Rust Proof Co | Pretreatment solution for phosphate coating, method of preparing the same and process of treating metal surfaces |
US2935423A (en) * | 1956-09-25 | 1960-05-03 | William H Kapfer | Process for applying a protective coating to a magnesium surface |
US2939809A (en) * | 1956-12-07 | 1960-06-07 | Douglas Aircraft Co Inc | Dry film lubrication |
US2975082A (en) * | 1957-01-22 | 1961-03-14 | John A Henricks | Method of providing ferrous articles with phosphate coatings and compositions therefor |
US2984592A (en) * | 1958-03-19 | 1961-05-16 | Chem Metals Inc | Protective coatings for galvanized members |
US2980553A (en) * | 1958-06-23 | 1961-04-18 | Smith Corp A O | Glass coated steel article and method of making the same |
US3015593A (en) * | 1960-10-04 | 1962-01-02 | Jayne John Phillip | Methods and composition for producing a phosphate coating on zinc metal |
US3152018A (en) * | 1961-11-01 | 1964-10-06 | Wyandotte Chemicals Corp | Room temperature phosphate coating composition |
US3904346A (en) * | 1971-12-23 | 1975-09-09 | Leslie Earl Shaw | Electrostatic powder coating process |
FR2492413A1 (en) * | 1980-10-22 | 1982-04-23 | Chaffoteaux Et Maury | Pyrophosphate conversion coating of zinc surface - using pyrophosphate- and nitrate-contg. soln. of controlled pH |
FR2531457A1 (en) * | 1982-08-03 | 1984-02-10 | Roquette Freres | SOLUTION AND PROCESS FOR THE CHEMICAL CONVERSION OF METAL SUBSTRATES |
EP0946786A1 (en) * | 1996-11-27 | 1999-10-06 | Henkel Corporation | Aqueous composition and process for preparing metal substrate for cold forming |
EP0946786A4 (en) * | 1996-11-27 | 1999-10-06 | ||
US6068710A (en) * | 1996-11-27 | 2000-05-30 | Henkel Corporation | Aqueous composition and process for preparing metal substrate for cold forming |
US20150340138A1 (en) * | 2009-02-24 | 2015-11-26 | Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) | Iron-based soft magnetic powder for dust core, method for manufacturing the same, and dust core |
US10256019B2 (en) * | 2009-02-24 | 2019-04-09 | Kobe Steel, Ltd. | Iron-based soft magnetic powder for dust core, method for manufacturing the same, and dust core |
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