CA2336186A1 - Method for inhibiting stains on aluminum product surfaces - Google Patents
Method for inhibiting stains on aluminum product surfaces Download PDFInfo
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- CA2336186A1 CA2336186A1 CA002336186A CA2336186A CA2336186A1 CA 2336186 A1 CA2336186 A1 CA 2336186A1 CA 002336186 A CA002336186 A CA 002336186A CA 2336186 A CA2336186 A CA 2336186A CA 2336186 A1 CA2336186 A1 CA 2336186A1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/18—Processes for applying liquids or other fluent materials performed by dipping
- B05D1/185—Processes for applying liquids or other fluent materials performed by dipping applying monomolecular layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- 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
- C23C22/02—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 non-aqueous solutions
- C23C22/03—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 non-aqueous solutions containing phosphorus compounds
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
- C23C22/20—Orthophosphates containing aluminium cations
-
- C—CHEMISTRY; METALLURGY
- 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
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/167—Phosphorus-containing compounds
- C23F11/1676—Phosphonic acids
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Nanotechnology (AREA)
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- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Composite Materials (AREA)
- Manufacturing & Machinery (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Chemical Treatment Of Metals (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
A method for inhibiting the formation of stains, especially water stains, on the exterior surfaces of aluminum alloy products. The method entails contacting the exterior surfaces of these products, particularly sheet or plate products, extrusions and/or forgings made from 5000 or 6000 Series aluminum alloys, with an organophosphonic or organophosphinic acid-derived material. Preferably, liquid forms of this material are added to an alcohol or water-based carrier solution, then sprayed, dipped, painted or rolled onto the surfaces of flat sheet or plate products to enhance their brightness. Other more complex shapes may be dipped into material baths.
Description
METHOA FOR INHIB~G STAINS
ON ALUMIrIUNX PRODUCT SURFACES
Water stains do not generally present problems for the structural properties and/or corrosion performance of an aluminum product. Aluminum surface discolorations that accompany water staining may discomfort some customers who are unfamiliar with the surface and corrosion properties of aluminum. Customers already aware of the properties of cold rolled steel may mistakenly believe that water stains on aluminum are the onset of "rusting", similar to that found on steel. For bright aluminum products, such as buffed trailer plate, rail cars, tool boxes, running boards, and tread plate on fire trucks, stain inhibition would preserve the buffed finish and enhance customer satisfaction. A
simple, low-cost solution to inlu'bit water stain on aluminum could result in a higher degree of customer confidence in replacing stool with alu~oainum for their products. In addition, arsthelics of these products is important to the end customer. Waxer star are aesthetically unattractive and their elimination or reduction would be valuable to the owner whether it be an aluminum trailer, rail car, tool box or other aluminum product.
Numerous uses for organophosphonic acids in conjunction with aluminum arc iaaown. These include U.S. Patent Nos. 4,957,890, 5,032,237, 5,059,258, 5,103,550, 5,124,022, 5,124,289, 5,126,210, 5,132,181, 5,238,715, 5,277,788 and 5,463,804. None of these, however, mention organophasphonic acids for the inhibition of stains, especially water stains, on aluminum surfaces. Most of the aforementioned patents describe aluminum surface pretreatments that enhance the durability of organic coatings or adhesively bonded joints. They do not describe the use of organophosphonics without a topcoat Other methods for inhibiting coaosion with respect to aluminum and other metals are disclosed in U.S. Patent Nos. 3,433,577, 3,672,822 and 4,427,448_ This invention addresses a low cost method for inhibiting water staining on 5000 Series, or SXXX, aluminum. alloys, most notably 5083-H321 and 5454-H32 aluminum (Aluminum Association dcsigaations). Such alloys are used to make rail hopper cars and buffed trailer tanks. Similar surprising and unexpected results have been observed when this method was practiced on 6000 Series aluminum alloys, like the 6061-T6 alloys used to make various products including vehicle wheels. According to this method, it was determined that spraying a solution consisting of about 0.25 w~/o oct~decylphosphonic acid (or "ODPA") in an isopropanol solvent (or other medium) onto these aluminum alloy products, then allowing the alcohol to evaporate, is effective for inhibiting water staining. Similar effects were subsequently observed with a carrier composition containing octylphospbonic acid (or "OPA"). Suitable liquid carriers include alcohols, ketoses, ethers, aldchydcs, alkanes, and other organic solvents witb sufficient solubility for the organophosphonic acids. These organophosphonic acid-derived solutions can be applied to the metal surface by spraying, dipping, painting, or roll coating. It is also recognized that the stain inhibitor component can be delivered to the aluminum surfaces from various compositions used in the manufacture of alumiunum parts, including but not limited to: aqueous suspensions or solutions; metal forming lubricants, and metal cleaning andlor rinsing formulations; a buffing compound or wax that incorporates the stain inhibitor, metal heat treatment quench waters, and/or post-rinsing polisherslseal,ants or the like_ For certain stain inb,ibitor compounds, it is possible to buff a paste-like stain inhibitor directly onto the aluminum product surface.
Farther features, objectives and advantages of the present invention will be made clearer from the following detailed description made with reference to the drawing in which:
The FIGURE shows the schematic formation and orientation of hydrolytically .stable Al-O-P bonds of the stain inhibitor, octylphosphonic acid (OPA), as a reaction product with an oxidized aluminum surface for effecting the stain inbz'bition obseivcd according to this invention.
Preliminary indications of the effectiveness of this invention, for inhibiting stains, were observed in an accelerated corrosion test that involved outgassing products of cthylvinylacetate plastic pellets (obtained from Millennium Petrochemicals), high humidity and temperature cycling. After 12 temperature cycles, no water stains were observed on 5000 Series alloy samples initially etched in caustic, then sprayed with an ODPA containing solution. Water staining was also inlu.'bited for "mill finish" metal sprayed with ODPA; though some spots were interspersed with unstained surface in the latter case. By cont<~ast, mill-finish and etched-only samples were completely covered with water stains. It is believed that the difference in performance as a result of pre-etching were most likely due to the removal of residual rolling lubricants via etching. In that manner, the stain inhibiting molecules of this invention would be allowed to chemically bond with surface aluminum oxides. .
Chemical reaction of the inhibitor to the surface can also be achieved by changing the means of application or using a different solvent. The surface ODPA
inhibits access of water to the aluminum oxide and forms hydrolytically stable bonds with the oxide, thus inhibiting water staining. ODPA is a commercial compound manufactured and sold by Albright & Wilson Ltd. Working solation concentrations and surface coverages of this invention are relatively low, which results in low gent costs of cents per square foot of A1 plate or sheet product. The same would be true for other aluminum product forms, including castings, forgings and extensions.
Another potential stain inhibitor, octylphosphonic acid (OPA), was evaluated. It showed even better performance results than the ODPA samplings above.
OPA has the following chemical sflructure: CH3(CH2)~P(O)(OH)z. It can be applied with a water and surfactant carrier as effectively as with an isopropanol carrier.
OPA is more soluble than ODPA in isopropanol thus allowing for increased solution concentrations.
And while OPA is not water soluble, it fo:ms a suspension of solids with water. In either case, no volatile organic carbons (ar VOC's) result therefrom.
Preliminary humidity test results show that OPA is highly effective for inhibiting stains on mill finish or buffed aluminum products without cleaning, pic~g or pre-etching. After three hours at 50°C (125°F~ and 100% relative humidity, the OPA
treated surface was unstained, where ~~-bnged'~, untreated surfaces were considerably stained.
It may also be possible to apply certain foimuIations by the methods of this invention with no carrier solution. For example, one may directly buff a more solid form of OPA onto an aluminum product surface. It is also possible, actually even more practical depending on the aluminum surface to be treated, to incorporate the stain inhibiting compounds of this invention into mill lubricants for providing an in situ type of stain inhibition and cIinninating subsequent processing steps. it may also be possible to similarly add such stain inhibitors to bung, sealing and/or polishing compound formulations.
When the aluminum to be treated is mill finish or "as buffed", a preferred carrier/solvent is an alcohol, more preferably 2-propanol or isopropaaol.
Isopropanol is also beneficial in that its solvent action is betievcd to displace residual mill lubricants or buffing compounds and wet the surface aluminum resulting in the formation of Al-O P
bonds with the oxidized aluminum surface. Isopropanol is also non toxic. When the aluminum surface has been pro-cleaned or etched, the choice of solvent is not as critical.
In many instances, water may be used to transport (or apply) such stain inln'bitors.
In addition to forming hydrolytically stable Al-O-P bonds, organophosphonic acids may provide yet another mechanism for stain inhibition.
For example, when OPA or ODPA reacts on the A1 surface, the reaction end product is believed to orient or align so that its hydrocarbon chains extend away from said surface.
A schematic representation of the bonding tliat is believed to take place is shown in the accompanying FIGURE. The latter surface takes on a "hydrophobic" or non-wetting quality thereby further inhibiting the conversion of oxides to hydroxides (or effecting a water stain thereon). Under the latter scenario, longer chained organophosphonic acids become the preferred stain inhibitors for this invention.
In some embodiments of this invention, a foil (and not partial or non-uniform) haze on the aluminum product surface may form. It is preferred that such haze be wiped away with a dry cloth to further enhance stain inhibition. On a less preferred basis, this haze may removed by rinsing the aluminum product's outer surface.
Certain classes of phosphorus oxo acids, acid esters, aiid acid salts arc effective to various degrees in preventing water stains according to this invention.
Phosphate salts, phosphate esters, and phosphoric acids cacti impart some stain inhibition. In comparative tests, however, octadecylphosphonic (C-18} acid (01~PA) and several fluoro phosphoric acids were not as effective as OPA (C-8) in inhibiting stains.
Poly(vinylphosphonic acid), and copoiymcrs thereof, may work even better than OPA, but it is currently cost prohibitive to use in commercial quantities. Some of the representative stain inhibitors can be grouped by the following "families":
a) acidic aluminum phosphate salts ~o I
(NHJi ~' QO ~ P - OH
O
dibasic ammonium phosphate b) inorganic phosphorus oxo acids OH OH H
HO-P-OH H-P-OH H-P-OH
Ip 1I IO
O
phosphoric acid phosphorous acid hypophosphorous acid c) organophosphonic and organophosphinic acids H OH
CH3 - (CH~,~ - P - OH CH3 - (CH~j~ - P - OH
II 'O
O
oc~adecylphosphonic and (ODPA) octylphosphonic acid (OPA) OH
I
CFs - (CF~s - P - OH CFs - (CF~S - P - OH
II
II O
O
perfluorohexylphosphonic acid perfluorohexylphosphinic acid (a component of the FluowetPP~ product sold by Hoechst-Celanese) d) phosphate acid esters_ op(o)(ot~z oP(O)(OH)~ ~ myo-inositolhexakis(dihydrogenphosphate) . ~ °r~~°~cvH~z "phytic acid'.
oP(o)(OH)~
OP(O)(OH)2 e) organo phosphoric acid polymers and copolymers; and for example, polyvinyl phosphoric-co-acrylic acid) ~ phosphate ester polymers for example, polyvinyl phosphoric acid) This invention can be used to improve the stain inhibition of numerous aluminum alloy surfaces, including various sheet or plate products, extrusions and forgings, regardless of whether such products have welded joints or other connections. It is best snitcd for any aluminum product that its purchaser, the end user/consumer, would prefer that said pmduct "look good" (i.e. brighter, less stained, etc.) longer! This includes a a whole family of building/architecwral products, appliances, lighting supplies, and other household cosmetics like vertical blind stock. On a preferred basis, the method of this invention works well with 5000 and 6000 Series alloys (Aluminum Association designation). It should also enhance the stain inhibiting performance of products made from other aluminum alloys,.including but not limited to 1000 and 3000 Series alloys.
t Stud - Several sections of buffed trailer tank plate product (made from 5454 aluminum alloy) were sprayed with two comparative stain inhibiting compositions:
Set 1: 0.2 wt% octyiphosphonic acid (OPA) in isopropanol; and Set 2: 0.2 wt% octadecylphosphonic acid (ODPA) in isopropanol.
Haze on both sets of sprayed plates was rinsed away with water, then gently buffed with dry cheesecloth. These treated plates, along with an "as-buffed" control, were then placed in a humidity cabinet at 50°C (I25°F) with 100% relative humidity for 3 hours.
After exposure, the plates were removed from the cabinet, dried with a towel, and visually examinrcd for staining.
No noticeable loss of specularity was observed with either of the above stain inhibition treatments. All surfaces had the same visual appearance as the "as-buffed" sample. After humidity exposure, however, brownish colored, water stains were evident over a majority of the "as-buged" and ODPA-treated surfaces. The OPA
treated surface did not exhibit any water stains and appeared the same as unexposed specimens.
While ODPA specimens did not fare as well as OPA in this particular study, as compared with its earlier positive results, different application techniques arc believed to have caused its reduced stain inhibiting performance here.
Second Studv - Tanker Trial results A covered hopper trailer, made from 5454 aluminum Bulk Transportation Sheet ('BTS") was treated with various applications according to the invention before being exposed to harsh, in-service conditions: From an aggressive environment of salt air due to seacoast proximity, and harsh winter conditions with numerous road salt applications. Subsections of this hopper/tanker were treated as follows: (a) 1 wt.%
solution of OPA, in isopropanol, was sprayed on the first section of tanker, dried to a filru, water rinsed and air deed thereafter, (b) the same solution as above was sprayed onto another adjoining section of the same hopper/tanker, then dried to a film and wiped to an initial shine using cheesecloth; (c) for this section of hopper/tanker, the treatment material was 1 wt% OPA, suspended in water. After spraying, this water-based solution was allowed to sit on the product surface for about 10 minutes before being dried and wiped to a shine with cheesecloth. The last comparative section of hopper/tanker was sprayed with a S wt.% solution of OPA, in water, before being allowed to sit for 10 minutes, then water rinsed and air dried.
After three months of service along the U.S. East Coast, this hopper/trailcr was brought back for inspection. While OPA treatments were observed to provide a substantial degree of water stain inhibition over that 3 month trial period, one of the first io conclusions drawn from that inspcckioa was that monthly reapplications could ensure a pristine, polished surface on such trailer stock.
Following a wash with non etching alkaline cleaner, various sides and subsections of this hoppcr/tanker were photographed and closely compared by visual inspection. From that inspection, it was noted that the water-based sections of treated hopper fared better than their alcohol-based counterparts (in terms of water staining inhibition). In. addition, wiping to a shine after application of the OPA, as per example (a) above, was most effective, even more than merely applying, rinsing and air drying, the latter trea~m~ent resulting in a noticeable, residual haze at first Third Stuliy - Coil Line Trial A coil of 5182-H19 aluminum sheet was roll coated with a 5% aqueous suspension of OPA. Phosphorus surface concentrations were measured on the treated surface using X-ray fluorescence spectroscopy (X~. From previous bench scale tests, it was observed that phosphorus surface levels of about 2 Kcps were sufficient for inhibiting water staining. Phosphorus surface levels on the aforementioned sheet product were measured at about 10 Kcps, however.
Fourth Studv - Forged Truck Wheels Forged and polished truck wheels made from aluminum alloy 6061-T6 were treated with comparative solutions of 0.5 and 1 wt% OPA in isopropanol. For testing, the treated wheels were placed into a cabinet with condensing humidity set at 100°F. The wheels were examined every hour for water stains. The tests were stopped after 120 hours of m humidity exposure. Untreated wheels (as-polished) were substantially stained within I 1 hours of humidity exposure. The wheels that were treated with OPA, then buffed to shine lasted the longest without substantial water staining. On certain OPA-treated wheels, only a few small, widely dispersed spots were observed after 120 hours of exposure testing, but that level of staining was insi~ificant compared to the gross quantities of water sting observed on the untreated wheels after only 11 hours of humidity exposure.
fifth Study - Lighting Sheet Aluminum alloy 5657-H18, used for making bright lighting sheet, was treated with a 5 wt.% solution of OPA stain inhibitor in isopropanol. Specular reflectance measurements showed that after buffing the resultant haze from said sheet surfaces, the OPA treatment did not reduce reflectivity. Furthermore, such OPA
treated panels lasted up to 13 days in condensing humidity at 100°F without staining, as compared to their untreated sheet equivalents that were significantly stained within 24 hours of such humidity exposure.
ixth Studv - Quench Water Additions Phosphorus compounds, like those described above, were added to the quench waters used for making extruded tubes and rolled sheet from 6061-T6 alloy. In this comparison, the aluminum product forms were heated to about 1U00°F
before being cold water quenched, said quenching solution containing various phosphorus compounds.
Thereafter, those products were allowed to remain in the quench water for 24 hours. By visually examining these aluminum product forms, and by further measuring the amount of hydroxides formed thereon using Fouricr-transform infrared spectroscopy (FT-TR), it was determined separately that 10 g/L solutions of dibasic ammonium phosphate -(NH~~HP04 - and 10 g/L phytic acid best prevented the formation of water stains on these products. ~TUcy also prevented the formation of bayetite powders on the interior aluminmn surfaces of these ext<vded tubes.
ON ALUMIrIUNX PRODUCT SURFACES
Water stains do not generally present problems for the structural properties and/or corrosion performance of an aluminum product. Aluminum surface discolorations that accompany water staining may discomfort some customers who are unfamiliar with the surface and corrosion properties of aluminum. Customers already aware of the properties of cold rolled steel may mistakenly believe that water stains on aluminum are the onset of "rusting", similar to that found on steel. For bright aluminum products, such as buffed trailer plate, rail cars, tool boxes, running boards, and tread plate on fire trucks, stain inhibition would preserve the buffed finish and enhance customer satisfaction. A
simple, low-cost solution to inlu'bit water stain on aluminum could result in a higher degree of customer confidence in replacing stool with alu~oainum for their products. In addition, arsthelics of these products is important to the end customer. Waxer star are aesthetically unattractive and their elimination or reduction would be valuable to the owner whether it be an aluminum trailer, rail car, tool box or other aluminum product.
Numerous uses for organophosphonic acids in conjunction with aluminum arc iaaown. These include U.S. Patent Nos. 4,957,890, 5,032,237, 5,059,258, 5,103,550, 5,124,022, 5,124,289, 5,126,210, 5,132,181, 5,238,715, 5,277,788 and 5,463,804. None of these, however, mention organophasphonic acids for the inhibition of stains, especially water stains, on aluminum surfaces. Most of the aforementioned patents describe aluminum surface pretreatments that enhance the durability of organic coatings or adhesively bonded joints. They do not describe the use of organophosphonics without a topcoat Other methods for inhibiting coaosion with respect to aluminum and other metals are disclosed in U.S. Patent Nos. 3,433,577, 3,672,822 and 4,427,448_ This invention addresses a low cost method for inhibiting water staining on 5000 Series, or SXXX, aluminum. alloys, most notably 5083-H321 and 5454-H32 aluminum (Aluminum Association dcsigaations). Such alloys are used to make rail hopper cars and buffed trailer tanks. Similar surprising and unexpected results have been observed when this method was practiced on 6000 Series aluminum alloys, like the 6061-T6 alloys used to make various products including vehicle wheels. According to this method, it was determined that spraying a solution consisting of about 0.25 w~/o oct~decylphosphonic acid (or "ODPA") in an isopropanol solvent (or other medium) onto these aluminum alloy products, then allowing the alcohol to evaporate, is effective for inhibiting water staining. Similar effects were subsequently observed with a carrier composition containing octylphospbonic acid (or "OPA"). Suitable liquid carriers include alcohols, ketoses, ethers, aldchydcs, alkanes, and other organic solvents witb sufficient solubility for the organophosphonic acids. These organophosphonic acid-derived solutions can be applied to the metal surface by spraying, dipping, painting, or roll coating. It is also recognized that the stain inhibitor component can be delivered to the aluminum surfaces from various compositions used in the manufacture of alumiunum parts, including but not limited to: aqueous suspensions or solutions; metal forming lubricants, and metal cleaning andlor rinsing formulations; a buffing compound or wax that incorporates the stain inhibitor, metal heat treatment quench waters, and/or post-rinsing polisherslseal,ants or the like_ For certain stain inb,ibitor compounds, it is possible to buff a paste-like stain inhibitor directly onto the aluminum product surface.
Farther features, objectives and advantages of the present invention will be made clearer from the following detailed description made with reference to the drawing in which:
The FIGURE shows the schematic formation and orientation of hydrolytically .stable Al-O-P bonds of the stain inhibitor, octylphosphonic acid (OPA), as a reaction product with an oxidized aluminum surface for effecting the stain inbz'bition obseivcd according to this invention.
Preliminary indications of the effectiveness of this invention, for inhibiting stains, were observed in an accelerated corrosion test that involved outgassing products of cthylvinylacetate plastic pellets (obtained from Millennium Petrochemicals), high humidity and temperature cycling. After 12 temperature cycles, no water stains were observed on 5000 Series alloy samples initially etched in caustic, then sprayed with an ODPA containing solution. Water staining was also inlu.'bited for "mill finish" metal sprayed with ODPA; though some spots were interspersed with unstained surface in the latter case. By cont<~ast, mill-finish and etched-only samples were completely covered with water stains. It is believed that the difference in performance as a result of pre-etching were most likely due to the removal of residual rolling lubricants via etching. In that manner, the stain inhibiting molecules of this invention would be allowed to chemically bond with surface aluminum oxides. .
Chemical reaction of the inhibitor to the surface can also be achieved by changing the means of application or using a different solvent. The surface ODPA
inhibits access of water to the aluminum oxide and forms hydrolytically stable bonds with the oxide, thus inhibiting water staining. ODPA is a commercial compound manufactured and sold by Albright & Wilson Ltd. Working solation concentrations and surface coverages of this invention are relatively low, which results in low gent costs of cents per square foot of A1 plate or sheet product. The same would be true for other aluminum product forms, including castings, forgings and extensions.
Another potential stain inhibitor, octylphosphonic acid (OPA), was evaluated. It showed even better performance results than the ODPA samplings above.
OPA has the following chemical sflructure: CH3(CH2)~P(O)(OH)z. It can be applied with a water and surfactant carrier as effectively as with an isopropanol carrier.
OPA is more soluble than ODPA in isopropanol thus allowing for increased solution concentrations.
And while OPA is not water soluble, it fo:ms a suspension of solids with water. In either case, no volatile organic carbons (ar VOC's) result therefrom.
Preliminary humidity test results show that OPA is highly effective for inhibiting stains on mill finish or buffed aluminum products without cleaning, pic~g or pre-etching. After three hours at 50°C (125°F~ and 100% relative humidity, the OPA
treated surface was unstained, where ~~-bnged'~, untreated surfaces were considerably stained.
It may also be possible to apply certain foimuIations by the methods of this invention with no carrier solution. For example, one may directly buff a more solid form of OPA onto an aluminum product surface. It is also possible, actually even more practical depending on the aluminum surface to be treated, to incorporate the stain inhibiting compounds of this invention into mill lubricants for providing an in situ type of stain inhibition and cIinninating subsequent processing steps. it may also be possible to similarly add such stain inhibitors to bung, sealing and/or polishing compound formulations.
When the aluminum to be treated is mill finish or "as buffed", a preferred carrier/solvent is an alcohol, more preferably 2-propanol or isopropaaol.
Isopropanol is also beneficial in that its solvent action is betievcd to displace residual mill lubricants or buffing compounds and wet the surface aluminum resulting in the formation of Al-O P
bonds with the oxidized aluminum surface. Isopropanol is also non toxic. When the aluminum surface has been pro-cleaned or etched, the choice of solvent is not as critical.
In many instances, water may be used to transport (or apply) such stain inln'bitors.
In addition to forming hydrolytically stable Al-O-P bonds, organophosphonic acids may provide yet another mechanism for stain inhibition.
For example, when OPA or ODPA reacts on the A1 surface, the reaction end product is believed to orient or align so that its hydrocarbon chains extend away from said surface.
A schematic representation of the bonding tliat is believed to take place is shown in the accompanying FIGURE. The latter surface takes on a "hydrophobic" or non-wetting quality thereby further inhibiting the conversion of oxides to hydroxides (or effecting a water stain thereon). Under the latter scenario, longer chained organophosphonic acids become the preferred stain inhibitors for this invention.
In some embodiments of this invention, a foil (and not partial or non-uniform) haze on the aluminum product surface may form. It is preferred that such haze be wiped away with a dry cloth to further enhance stain inhibition. On a less preferred basis, this haze may removed by rinsing the aluminum product's outer surface.
Certain classes of phosphorus oxo acids, acid esters, aiid acid salts arc effective to various degrees in preventing water stains according to this invention.
Phosphate salts, phosphate esters, and phosphoric acids cacti impart some stain inhibition. In comparative tests, however, octadecylphosphonic (C-18} acid (01~PA) and several fluoro phosphoric acids were not as effective as OPA (C-8) in inhibiting stains.
Poly(vinylphosphonic acid), and copoiymcrs thereof, may work even better than OPA, but it is currently cost prohibitive to use in commercial quantities. Some of the representative stain inhibitors can be grouped by the following "families":
a) acidic aluminum phosphate salts ~o I
(NHJi ~' QO ~ P - OH
O
dibasic ammonium phosphate b) inorganic phosphorus oxo acids OH OH H
HO-P-OH H-P-OH H-P-OH
Ip 1I IO
O
phosphoric acid phosphorous acid hypophosphorous acid c) organophosphonic and organophosphinic acids H OH
CH3 - (CH~,~ - P - OH CH3 - (CH~j~ - P - OH
II 'O
O
oc~adecylphosphonic and (ODPA) octylphosphonic acid (OPA) OH
I
CFs - (CF~s - P - OH CFs - (CF~S - P - OH
II
II O
O
perfluorohexylphosphonic acid perfluorohexylphosphinic acid (a component of the FluowetPP~ product sold by Hoechst-Celanese) d) phosphate acid esters_ op(o)(ot~z oP(O)(OH)~ ~ myo-inositolhexakis(dihydrogenphosphate) . ~ °r~~°~cvH~z "phytic acid'.
oP(o)(OH)~
OP(O)(OH)2 e) organo phosphoric acid polymers and copolymers; and for example, polyvinyl phosphoric-co-acrylic acid) ~ phosphate ester polymers for example, polyvinyl phosphoric acid) This invention can be used to improve the stain inhibition of numerous aluminum alloy surfaces, including various sheet or plate products, extrusions and forgings, regardless of whether such products have welded joints or other connections. It is best snitcd for any aluminum product that its purchaser, the end user/consumer, would prefer that said pmduct "look good" (i.e. brighter, less stained, etc.) longer! This includes a a whole family of building/architecwral products, appliances, lighting supplies, and other household cosmetics like vertical blind stock. On a preferred basis, the method of this invention works well with 5000 and 6000 Series alloys (Aluminum Association designation). It should also enhance the stain inhibiting performance of products made from other aluminum alloys,.including but not limited to 1000 and 3000 Series alloys.
t Stud - Several sections of buffed trailer tank plate product (made from 5454 aluminum alloy) were sprayed with two comparative stain inhibiting compositions:
Set 1: 0.2 wt% octyiphosphonic acid (OPA) in isopropanol; and Set 2: 0.2 wt% octadecylphosphonic acid (ODPA) in isopropanol.
Haze on both sets of sprayed plates was rinsed away with water, then gently buffed with dry cheesecloth. These treated plates, along with an "as-buffed" control, were then placed in a humidity cabinet at 50°C (I25°F) with 100% relative humidity for 3 hours.
After exposure, the plates were removed from the cabinet, dried with a towel, and visually examinrcd for staining.
No noticeable loss of specularity was observed with either of the above stain inhibition treatments. All surfaces had the same visual appearance as the "as-buffed" sample. After humidity exposure, however, brownish colored, water stains were evident over a majority of the "as-buged" and ODPA-treated surfaces. The OPA
treated surface did not exhibit any water stains and appeared the same as unexposed specimens.
While ODPA specimens did not fare as well as OPA in this particular study, as compared with its earlier positive results, different application techniques arc believed to have caused its reduced stain inhibiting performance here.
Second Studv - Tanker Trial results A covered hopper trailer, made from 5454 aluminum Bulk Transportation Sheet ('BTS") was treated with various applications according to the invention before being exposed to harsh, in-service conditions: From an aggressive environment of salt air due to seacoast proximity, and harsh winter conditions with numerous road salt applications. Subsections of this hopper/tanker were treated as follows: (a) 1 wt.%
solution of OPA, in isopropanol, was sprayed on the first section of tanker, dried to a filru, water rinsed and air deed thereafter, (b) the same solution as above was sprayed onto another adjoining section of the same hopper/tanker, then dried to a film and wiped to an initial shine using cheesecloth; (c) for this section of hopper/tanker, the treatment material was 1 wt% OPA, suspended in water. After spraying, this water-based solution was allowed to sit on the product surface for about 10 minutes before being dried and wiped to a shine with cheesecloth. The last comparative section of hopper/tanker was sprayed with a S wt.% solution of OPA, in water, before being allowed to sit for 10 minutes, then water rinsed and air dried.
After three months of service along the U.S. East Coast, this hopper/trailcr was brought back for inspection. While OPA treatments were observed to provide a substantial degree of water stain inhibition over that 3 month trial period, one of the first io conclusions drawn from that inspcckioa was that monthly reapplications could ensure a pristine, polished surface on such trailer stock.
Following a wash with non etching alkaline cleaner, various sides and subsections of this hoppcr/tanker were photographed and closely compared by visual inspection. From that inspection, it was noted that the water-based sections of treated hopper fared better than their alcohol-based counterparts (in terms of water staining inhibition). In. addition, wiping to a shine after application of the OPA, as per example (a) above, was most effective, even more than merely applying, rinsing and air drying, the latter trea~m~ent resulting in a noticeable, residual haze at first Third Stuliy - Coil Line Trial A coil of 5182-H19 aluminum sheet was roll coated with a 5% aqueous suspension of OPA. Phosphorus surface concentrations were measured on the treated surface using X-ray fluorescence spectroscopy (X~. From previous bench scale tests, it was observed that phosphorus surface levels of about 2 Kcps were sufficient for inhibiting water staining. Phosphorus surface levels on the aforementioned sheet product were measured at about 10 Kcps, however.
Fourth Studv - Forged Truck Wheels Forged and polished truck wheels made from aluminum alloy 6061-T6 were treated with comparative solutions of 0.5 and 1 wt% OPA in isopropanol. For testing, the treated wheels were placed into a cabinet with condensing humidity set at 100°F. The wheels were examined every hour for water stains. The tests were stopped after 120 hours of m humidity exposure. Untreated wheels (as-polished) were substantially stained within I 1 hours of humidity exposure. The wheels that were treated with OPA, then buffed to shine lasted the longest without substantial water staining. On certain OPA-treated wheels, only a few small, widely dispersed spots were observed after 120 hours of exposure testing, but that level of staining was insi~ificant compared to the gross quantities of water sting observed on the untreated wheels after only 11 hours of humidity exposure.
fifth Study - Lighting Sheet Aluminum alloy 5657-H18, used for making bright lighting sheet, was treated with a 5 wt.% solution of OPA stain inhibitor in isopropanol. Specular reflectance measurements showed that after buffing the resultant haze from said sheet surfaces, the OPA treatment did not reduce reflectivity. Furthermore, such OPA
treated panels lasted up to 13 days in condensing humidity at 100°F without staining, as compared to their untreated sheet equivalents that were significantly stained within 24 hours of such humidity exposure.
ixth Studv - Quench Water Additions Phosphorus compounds, like those described above, were added to the quench waters used for making extruded tubes and rolled sheet from 6061-T6 alloy. In this comparison, the aluminum product forms were heated to about 1U00°F
before being cold water quenched, said quenching solution containing various phosphorus compounds.
Thereafter, those products were allowed to remain in the quench water for 24 hours. By visually examining these aluminum product forms, and by further measuring the amount of hydroxides formed thereon using Fouricr-transform infrared spectroscopy (FT-TR), it was determined separately that 10 g/L solutions of dibasic ammonium phosphate -(NH~~HP04 - and 10 g/L phytic acid best prevented the formation of water stains on these products. ~TUcy also prevented the formation of bayetite powders on the interior aluminmn surfaces of these ext<vded tubes.
Claims (44)
1. A method for inhibiting formation of stains on an exposed exterior of an aluminum alloy product, said method comprising:
(a) contacting the exposed exterior with a material that is capable of forming a hydrolytically stable Al-O-P bond therewith, said material selected from the group consisting of an acidic aluminum phosphate salt; an inorganic phosphorus oxo acid; an organophosphonic or organophosphinic acid; a phosphate acid ester, an organophosphonic acid polymer or copolymer; and an organophosphate acid ester polymer or copolymer.
(a) contacting the exposed exterior with a material that is capable of forming a hydrolytically stable Al-O-P bond therewith, said material selected from the group consisting of an acidic aluminum phosphate salt; an inorganic phosphorus oxo acid; an organophosphonic or organophosphinic acid; a phosphate acid ester, an organophosphonic acid polymer or copolymer; and an organophosphate acid ester polymer or copolymer.
2. The method of claim 1 wherein the material consists essentially of an organophosphonic or organophosphinic acid.
3. The method of claim 2 wherein the material is a solid or semi-solid at room temperature and manually applied to the exposed exterior of the aluminum alloy product.
4. The method of claim 2 wherein the material is a liquid at room temperature and combined with a carrier selected from the group consisting of an alcohol, a ketone, as ether, an aldehyde, an alkane, water and mixtures thereof.
5. The method of claim 4 wherein the material consists essentially of octadecylphosphonic acid and the carrier includes isopropanol.
6. The method of claim 4 wherein the material consists essentially of octylphosphonic acid and the carrier is selected from the group consisting of isopropanol, water and mixtures thereof.
7. The method of claim 4 wherein said exposed exterior is contacted with an aqueous solution containing up to about 10 wt% octadecylphosphonic acid, about 5 -90 wtf% isopropanol, a balance of water and impurities.
8. The method of claim 4 wherein said exposed exterior is contacted with an aqueous solution containing up to about 10 wt.% octylphosphonic acid, about wt% isopropanol, a balance of water and impurities.
9. The method of claim 4 wherein said exposed exterior is contacted with an aqueous solution containing abort 0.5 -10 wt.% octylphosphonic acid, a balance of water and impurities.
10. The method of claim 4 wherein said contacting includes: spraying, dipping, painting or rolling material on said exposed exterior of said alloy product
11. The method of claim 10 wherein said material is incorporated into a composition for surface treating said alloy product.
12. The method of claim 11 wherein said composition is selected from the group consisting of a mill lubricant, a quenching solution, an intermediate rinse, an etching solution, a solvent, a surfactant, a cleaner, a polish, a post-rinse, a sealant and mixtures thereof.
13. The method of claim 2 wherein said alloy product is selected from the group consisting of sheet product, plate product, an extrusion and a forging.
14. The method of claim 13 wherein said sheet or plate product has at least one bright exterior surface and is suitable for making transportation goods therefrom, said goods selected from the group consisting of: trailer plate, rail car skin, tool boxes, vehicle running boards and tread plate.
15. The method of claim 13 wherein said sheet product is used to make reflective lighting sheet.
16. The method of claim 13 wherein said treated extrusions can be used to make transportation or household goods therefrom, said goods selected from the group consisting of truckbed rails, hydraulic tubing, window frames, tab and shower frames, and greenhouse structural supports.
17. The method of claim 13 wherein said alloy product is a vehicle wheel.
18. The method of claim 1 which further includes: (b) rinsing material from the exposed exterior.
19. The method of claim 18 which further includes:
(c) wiping said exposed exterior.
(c) wiping said exposed exterior.
20. The method of claim 1 which further includes: (b) wiping material from the exposed exterior.
21. The method of claim 1 wherein said alloy product is made from a 1000, 3000, 5000 or 6000 Series aluminum alloy (Aluminum Association designations).
22. The method of claim 21 wherein said 5000 Series aluminum alloy is selected from the group consisting of 5083, 5086, 5454, 5657, 5182, and 5454 aluminum (Aluminum.Association designations).
23. The method of claim 21 wherein said 6000 Series aluminum alloy is selected from the group consisting of: 6061, 6111 and 6022 aluminum (Aluminum Association designations).
24. A method for inhibiting the formation of water stains on the exterior surfaces of a 5000 or 6000 Series aluminum alloy product, said method comprising:
(a) contacting the exterior surfaces with an organophosphonic or organophosphinic acid-derived material.
(a) contacting the exterior surfaces with an organophosphonic or organophosphinic acid-derived material.
25. The method of claim 24 wherein said acid-derived material is a solid or semi-solid at room temperature and manually applied to said exterior surfaces.
26. The method of claim 24 wherein said acid-derived material is a liquid at room temperature and combined with a carrier selected from the group consisting of an alcohol, a ketone, an ether, an aldehyde, an alkane, water and mixtures thereof.
27. The method of claim 26 wherein said acid-derived material consists essentially of octadecylphosphonic acid and said carrier includes isopropanol.
28. The method of claim 26 wherein said acid-derived material consists essentially of octylphosphonic acid and said easier is selected from the group consisting of: isopropanol, water and mixtures thereof.
29. The method of claim 26 wherein said exterior surfaces are contacted with an aqueous solution containing up to about 10 wt% octadecylphosphonic acid, about 5 - 90 wt% isopropanol, the balance water and impurities.
30. The method of claim 26 wherein said exterior surfaces are contacted with an aqueous solution containing up to about 10 wt.% octylphosphonic acid, about 5 -90 wt% isopropanol, the balance water and impurities.
31. The method of claim 26 wherein said exterior surfaces are contacted with an aqueous solution containing about 0.5 -10 wt.% octylphosphonic acid, the balance water and impurities.
32. The method of claim 24 wherein said contacting includes: spraying, dipping, painting or rolling material onto said exterior surfaces.
33. The method of claim 24 wherein said acid-derived material is incorporated into a composition used to manufacture said aluminum alloy product.
34. The method of claim 33 wherein said composition is selected from the group consisting of a mill lubricant, a quenching solution, as intermediate rinse, an etching solution, a solvent, a surfactant, a cleaner, a polish, a post-rinse, a sealant and mixtures thereof.
35. The method of claim 24 wherein said alloy product is selected from the group consisting of sheet product, plate product, an extrusion and a forging.
36. The method of claim 35 wherein said sheet or plate product has at least one bright exterior surface and is suitable for making transportation goods therefrom, said goods selected from the group consisting of trailer plate, rail car skin, tool boxes, vehicle running boards and tread plate.
37. The method of claim 35 wherein said sheet product is used to make reflective lighting sheet.
38. The method of claim 35 wherein said extrusion is subsequently into a transportation or household flood selected from the group consisting of truckbed rails, hydraulic cubing, window frames, tub and shower frames, and greenhouse structural supports.
39. The method of claim 35 wherein said alloy product is a vehicle wheel.
40. The method of claim 24 which further includes: (b) rinsing material from the exposed exterior.
41. The method of claim 40 which further includes:
(c) wiping said exposed exterior.
(c) wiping said exposed exterior.
42. The method of claim 24 which further includes: (b) wipe material from the exposed exterior.
43. The method of claim 24 wherein said 5000 Series aluminum alloy is selected from the group consisting of: 5083, 5086, 5454, 5657, 5182, and 5454 aluminum (Aluminum Association designations).
44. The method of claim 24 wherein said 6000 Series aluminum alloy is selected from the group consisting of 6061, 6111 and 6022 aluminum (Aluminum Association designations).
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9001798P | 1998-06-19 | 1998-06-19 | |
US33567699A | 1999-06-18 | 1999-06-18 | |
US60/090,017 | 1999-06-18 | ||
PCT/US1999/013827 WO1999066104A2 (en) | 1998-06-19 | 1999-06-18 | Method for inhibiting stains on aluminum product surfaces |
US09/335,676 | 1999-06-18 |
Publications (1)
Publication Number | Publication Date |
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CA2336186A1 true CA2336186A1 (en) | 1999-12-23 |
Family
ID=26781347
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002336186A Abandoned CA2336186A1 (en) | 1998-06-19 | 1999-06-18 | Method for inhibiting stains on aluminum product surfaces |
Country Status (7)
Country | Link |
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US (1) | US20020011280A1 (en) |
EP (1) | EP1088119A2 (en) |
JP (1) | JP2002518594A (en) |
AU (1) | AU4695799A (en) |
BR (1) | BR9912174A (en) |
CA (1) | CA2336186A1 (en) |
WO (1) | WO1999066104A2 (en) |
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US7018486B2 (en) † | 2002-05-13 | 2006-03-28 | United Technologies Corporation | Corrosion resistant trivalent chromium phosphated chemical conversion coatings |
US20050268991A1 (en) * | 2004-06-03 | 2005-12-08 | Enthone Inc. | Corrosion resistance enhancement of tin surfaces |
FR2904241B1 (en) | 2006-07-31 | 2008-10-03 | Inst Francais Du Petrole | PROCESS FOR THE PREPARATION OF MATERIALS BY GRATING HALOGEN PHOSPHORUS GROUPS ON AN INORGANIC SURFACE |
US7883738B2 (en) * | 2007-04-18 | 2011-02-08 | Enthone Inc. | Metallic surface enhancement |
US10017863B2 (en) * | 2007-06-21 | 2018-07-10 | Joseph A. Abys | Corrosion protection of bronzes |
TWI453301B (en) * | 2007-11-08 | 2014-09-21 | Enthone | Self assembled molecules on immersion silver coatings |
US7972655B2 (en) * | 2007-11-21 | 2011-07-05 | Enthone Inc. | Anti-tarnish coatings |
FR3026412B1 (en) * | 2014-09-26 | 2019-03-29 | Aperam | SURFACE TREATMENT OF METAL SUBSTRATES |
US10645959B2 (en) * | 2016-09-19 | 2020-05-12 | Red Bull Gmbh | Method and device for treating and monitoring the quality of objects comprising metal materials |
CN106884165B (en) * | 2017-01-13 | 2019-03-22 | 清华大学 | A method of based on the modified raising material against oxidative ablation property of surface micro-structure |
TWI714285B (en) * | 2018-09-27 | 2020-12-21 | 日商Toto股份有限公司 | Sanitary equipment parts |
JP6763463B1 (en) * | 2018-09-27 | 2020-09-30 | Toto株式会社 | Faucet fitting |
EP4140304A1 (en) * | 2019-05-31 | 2023-03-01 | Rolex S.A. | Composition for impregnating a substrate, in particular a watchstrap |
JP7331592B2 (en) * | 2019-09-27 | 2023-08-23 | Toto株式会社 | Method for manufacturing sanitary equipment member having organic layer formed on surface |
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US2901821A (en) * | 1955-11-18 | 1959-09-01 | Detrex Chem Ind | Aluminum coated with aluminum benzoate, and method and composition for making same |
US3985584A (en) * | 1972-10-25 | 1976-10-12 | Oakite Products, Inc. | Metal protective coating compositions, their preparation and use |
JPS5315687B2 (en) * | 1973-10-04 | 1978-05-26 | ||
DE2519132C3 (en) * | 1974-05-02 | 1982-03-04 | Fuji Sashi Industries Ldt., Kawasaki, Kanagawa | Process for the continuous production of surface-protected extruded fittings made of aluminum or aluminum alloys |
CA1083756A (en) * | 1975-08-07 | 1980-08-19 | George P. Koch | Prevention of water staining of aluminum |
JPS5273139A (en) * | 1975-12-16 | 1977-06-18 | Nippon Steel Corp | Chemical conversion process for metallic material |
ATE4465T1 (en) * | 1979-01-22 | 1983-09-15 | Ball Corporation | A SOLUTION TO PREVENT TARNISHING OF ALUMINUM SURFACES AND HOW TO APPLY IT. |
JPS5839232B2 (en) * | 1980-05-12 | 1983-08-29 | 日本パ−カライジング株式会社 | Film chemical conversion treatment solution for aluminum and aluminum alloy surfaces |
US4846898A (en) * | 1988-05-05 | 1989-07-11 | Amax Inc. | Method of rendering aluminum base metal resistant to water staining |
JPH0778280B2 (en) * | 1988-07-28 | 1995-08-23 | 株式会社日立製作所 | Metal anti-corrosion surface treatment method |
JPH0266177A (en) * | 1988-08-31 | 1990-03-06 | Kobe Steel Ltd | Treatment of aluminum or aluminum alloy with hot water |
BR9106572A (en) * | 1990-06-19 | 1993-06-01 | Henkel Corp | LIQUID COMPOSITION AND PROCESS FOR TREATING TIN OR ALUMINUM COATED STEEL SURFACES TO CONFER MOBILITY AND CORROSION RESISTANCE |
US5279677A (en) * | 1991-06-17 | 1994-01-18 | Coral International, Inc. | Rinse aid for metal surfaces |
GB2259920A (en) * | 1991-09-10 | 1993-03-31 | Gibson Chem Ltd | Surface conversion coating solution based on molybdenum and phosphate compounds |
DE4443032A1 (en) * | 1994-12-02 | 1996-06-05 | Haca Gmbh Verschleisteil Techn | Solid surface treatment agent containing a solvent and a fluorine-containing substance as an active agent |
JP3544761B2 (en) * | 1995-10-13 | 2004-07-21 | 日本パーカライジング株式会社 | Surface treatment composition for aluminum-containing metal material and surface treatment method |
US5601663A (en) * | 1996-02-22 | 1997-02-11 | General Motors Corporation | Process for forming a black oxide on aluminum alloys and a solution therefor |
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1999
- 1999-06-18 BR BR9912174-3A patent/BR9912174A/en not_active IP Right Cessation
- 1999-06-18 AU AU46957/99A patent/AU4695799A/en not_active Abandoned
- 1999-06-18 EP EP99930410A patent/EP1088119A2/en not_active Ceased
- 1999-06-18 WO PCT/US1999/013827 patent/WO1999066104A2/en not_active Application Discontinuation
- 1999-06-18 JP JP2000554905A patent/JP2002518594A/en not_active Withdrawn
- 1999-06-18 CA CA002336186A patent/CA2336186A1/en not_active Abandoned
-
2001
- 2001-05-29 US US09/866,953 patent/US20020011280A1/en not_active Abandoned
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BR9912174A (en) | 2001-04-10 |
WO1999066104A3 (en) | 2000-03-30 |
US20020011280A1 (en) | 2002-01-31 |
WO1999066104A2 (en) | 1999-12-23 |
JP2002518594A (en) | 2002-06-25 |
AU4695799A (en) | 2000-01-05 |
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