US 4,242,379 AGrant
Acid Inhibitor Treatment of Substrate Prior to Autodeposition
Issue Date:1980-12-30
•10 Claims
Abstract
A metallic substrate is pretreated with a composition containing an acid corrosion inhibitor prior to subjecting the substrate to an acidic aqueous autodepositing coating composition of the type which contains dissolved fluoride and ferric ions in order to improve the quality of the coating formed from said autodepositing composition by reducing or preventing the tendency of the composition to form coatings which contain pinholes or blisters on worked or roughened areas of the metallic surface.
Metadata
Assignee
- Amchem Products, Inc.
Inventors
- Wilbur S. Hall
- Harry M. Leister
Application Information
Application Number:US 0559741
Filing Date:1979-07-10
Priority Date:1976-12-30
Art Unit:162
Classifications
IPC:
A23F 334
Field of Search:
1484271342526.2;6.15 R435;3272156;135
Patent Drawings
This patent does not have any drawings.
Description
Examples
Unless stated otherwise, the following autodepositing composition was used in the examples reported below.
The resin of the latex used in the above composition comprised about 62% styrene, about 30% butadiene, about 5% vinylider chloride and about 3% methacrylic acid. A film formed from the resin is soluble in refluxing chlorobenzene to the extent of about 13%. That the resin is cross-linked is indicated by its insolubility in Soxhlet extraction with chlorobenzene. The water soluble content of the latex is about 2% based on the weight of dried resin, with the water soluble content comprising about 10% sodium phosphate, about 13% sodium oleoyl isopropanolamide sulfosuccinate and about 75% sodium dodecylbenzene sulfonate, the first mentioned ingredient being a buffering agent used in preparing the latex, and the last two mentioned ingredients being emulsifiers. The pH of the latex was about 7.8 and the surface tension thereof about 45-50 dynes/cm. The average particle size of the resin was about 2,000 A.
The metal parts that were treated in the procedure described in the examples were sections of cold rolled steel mounting rings for automobile headlamps that were formed by a stamping operation. Each of the sections contained surface portions that were galled.
The pretreating solutions used in the first group of examples contained mercaptobenzothiazole (acid inhibitor) in the amounts indicated in Table 1 below and about 45 g/l of an alkaline cleaning material sold under the trademark Ridoline 1027 by Amchem Products, Inc. (The alkaline cleaning material comprised mainly sodium hydroxide and sodium tripolyphosphate.)
Sections of the mounting rings were immersed in the pretreating solutions identified in Table 1 below for 5 minutes at a temperature of 160.degree. F. and thereafter were rinsed with tap water. The sections were then immersed in the autodepositing composition described above for 75 seconds. After withdrawal from the composition, the coated sections were allowed to partially dry in air for about 1 minute and then were rinsed by immersion in tap water. The coated parts were then baked in an oven having a temperature of 120.degree. C. for 10 minutes. For comparative purposes, a section was pretreated with a pretreating solution that contained no acid inhibitor. Descriptions of the autodeposited coatings that were obtained are set forth in Table 1 below.
From Table 1 above, it can be seen that as the concentration of the acid inhibitor was increased, improvements in the qualities of the coatings were realized. The pinholes and craters that were present in the coatings were present in those portions that overlay the portions of the sections that were galled.
Example 5
The pretreating solution used in this example comprised an aqueous solution of alkaline cleaning materials and a mixture of inhibitors, namely sodium dichromate and sodium nitrite. The aqueous solution comprised:
A section of the aforementioned mounting ring was immersed in the pretreating solution for 30 seconds at a temperature of 160.degree. F. The pretreated section was then coated in the manner described above in connection with Examples 1 to 4. The autodeposited coating that was formed contained very few blisters and quite a few craters. This was an improvement over a section that was not so pretreated, but coated in the same way, which section had many pinholes in the coating overlying the gall marks of the section.
Example 6
Another section of mounting ring was treated in the same manner as the section of Example 5 except that the pretreating solution contained 10 g/l of sodium nitrite and 45 g/l of the alkaline cleaning solution described in Examples 1 to 4. The autodeposited coating that was formed was similar in appearance to the coating of the pretreated section described in Example 5.
Example 7
The pretreating solution used in this example contained 5 g/l of sodium dichromate dihydrate and 45 g/l of the alkaline cleaning material described in Examples 1 to 4. A section of mounting ring was immersed for 5 minutes in the pretreating solution at a temperature of 160.degree. F. The pretreated part was then rinsed with water and immersed for 75 seconds in an autodepositing coating composition like that used in the previous examples, except that the amount of latex was about 185 g/l and the composition contained 5 g/l of a black pigment dispersion having a total solids content of about 36%. Carbon black comprised about 30% of the dispersion which had a pH of about 10-11.5 and a specific gravity of about 1.17. The aqueous dispersion contained a nonionic dispersing agent for the solids, and is sold under the trademark Aquablak 115.
After withdrawing the coated section from the autodepositing composition, it was partially dried in air for about 1 minute, rinsed with water and baked for 10 minutes at a temperature of 220.degree. F. The coating contained no blisters, craters or pinholes. Another section of mounting ring was treated in exactly the same way, except that the pretreatment solution contained no sodium dichromate. Its coating contained pinholes and blisters in the portions that overlay the gall marks of the section.
Whereas the improvement in autodeposition described herein relies upon treating the metal surface with an acid corrosion inhibitor prior to contacting the metal surface with an autodepositing composition, it has also been found that a similar improvement can be obtained by adding an acid corrosion inhibitor to the autodepositing composition. The latter method is the subject of co-pending application Ser. No. 755,921 filed Dec. 30, 1976 and assigned to the same assignee:
Claims
We claim:
1. In a coating process wherein an autodeposited coating is formed on a worked or roughened metal surface by contacting said surface with an autodepositing composition comprising an acidic aqueous solution containing dissolved fluoride and ferric ions and having resin solids dispersed therein and wherein the coatings formed from said composition tend to contain defects, the improvement comprising treating said metal surface with an anodic acid inhibitor in an amount sufficient to passivate the anodic sites in the worked or roughened areas of said metal surface, said inhibitor not forming a detectable coating on said surface, prior to contacting said surface with said acidic coating composition.
2. In a coating process wherein an autodeposited resinous coating is formed on a worked metal surface or an unworked roughened metal surface by immersing said surface in an autodepositing composition comprising an acidic aqueous solution containing dissolved fluoride and ferric iron and having dispersed therein resin solids and wherein said composition tends to form on said surface coatings having defects, including blisters, craters, pinholes or uncoated portions of the metal surface, the improvement comprising contacting said metal surface with an aqueous alkaline cleaning solution having an acid corrosion inhibitor dissolved therein in an amount sufficient to passivate the anodic sites in the worked or roughened areas of said metal surface, said inhibitor not forming a detectable coating on said surface, prior to immersing said surface in said coating composition.
3. In a coating process wherein an autodeposited resinous coating is formed on a worked metal surface or an unworked roughened metal surface by immersing said surface in an autodepositing composition comprising an acidic aqueous solution containing dissolved fluoride and ferric iron and having dispersed therein resin solids wherein said composition tends to form on said surface coatings having defects, including blisters, craters, pinholes or uncoated portions of the metal surface, the improvement comprising contacting said metal surface with an aqueous alkaline cleaning solution having dissolved therein about 0.3 to about 5 wt. % of an organic acid inhibitor, said inhibitor not forming a detectable coating on said surface, prior to immersing said surface in said composition.
4. The process of claim 3 wherein the aqueous alkaline cleaning solution comprises an aqueous solution of sodium hydroxide and sodium tripolyphosphate.
5. The process of claim 4 wherein the organic acid inhibitor is mercaptobenzothiazole.
6. The process of claim 4 wherein the organic acid inhibitor is the product of a Mannich reaction of an amine derived from pine resin acids, acetone and formaldehyde and reacted in the presence of hydroxyacetic acid.
7. In a coating process wherein an autodeposited resinous coating is formed on a worked metal surface or an unworked roughened metal surface by immersing said surface in an autodepositing composition comprising an acidic aqueous solution containing dissolved fluoride and ferric iron and having dispersed therein resin solids and wherein said composition tends to form on said surface coatings having defects, including blisters, craters, pinholes or uncoated portions of the metal surface, the improvement which comprises contacting said metal surface which is free of acid removable soils with an aqueous alkaline cleaning solution having dissolved therein about 0.3 to about 5 wt. % of an acid inhibitor selected from the group consisting of chromates and dichromates, and mixtures thereof, to form a clean metal surface free of any detectable surface coating which is thereafter immersed in said coating composition to form a resinous coating thereon.
8. The process of claim 7 wherein the alkaline cleaning solution comprises a solution of sodium hydroxide and sodium phosphate.
9. A coating process comprising: (A) contacting a clean metal surface, wherein at least a portion of said surface is worked or roughened, with an acid corrosion inhibitor selected from the group consisting of organic acid inhibitors, chromates and dichromates and mixtures thereof said inhibitor not forming a detectable coating on said surface; and thereafter, (B) forming on said surface an autodeposited coating by contacting said surface with an autodepositing composition comprising an acidic aqueous solution containing fluoride and ferric iron and having resin solids dispersed therein.
10. A process according to claim 9 wherein said acid corrosion inhibitor is combined with an alkaline cleaning solution and is present in an amount between about 0.1% and about 1.0% by weight of said cleaning solution.
Patent Citations (6)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US1279101 | 1918-09-01 | Gravell | |
| US2304299 | 1942-12-01 | Boyle et al. | |
| US3585084 | 1971-06-01 | Steinbrecher et al. | |
| US3900601 | 1975-08-01 | Franz et al. | |
| US3973998 | 1976-08-01 | Datta et al. | |
| ZAX741124 | 1974-02-01 |
Non-Patent Literature (1)
- Kirk-Othmer, Encycl. of Chem. Tech., 2nd Ed., vol. 6, pp. 324, 343, vol. 13, pp. 286, 287 (1965).