IP Library Granted Patent US 10,472,525
Granted Patent B2
US 10,472,525 · App. 15/048,090 · Granted Nov 12, 2019

Use of dithiophosphinic acid and/or its salts for producing anti-corrosion coatings that are devoid of chrome

Inventors: Monica Fernandez Gonzalez (Frankenthal, DE); Markus Hickl (Münster, DE); Cordula Mock-Knoblauch (Lantau Island, CN); Manfred Essig (Otterberg, DE); Wolfgang Schrepp (Heidelberg, DE); Manfred Biehler (Ilbesheim, DE)
Assignee: BASF COATINGS GMBH
C09D5/086C09D133/14C23F11/167
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Quick Facts
Patent No.
US 10,472,525
App. No.
15/048,090
Granted
Nov 12, 2019
Kind
B2
Abstract

Use of dithiophosphinic acids of the general formula HS 2 P(R 1 )(R 2 ) and/or salts thereof for producing chrome-free, polymer-containing corrosion control layers on metallic surfaces, R 1 and R 2 independently of one another each being organic radicals having 1 to 30 C atoms.

Claims (18)

1. A coating in combination with a metallic surface, the coating comprising a radiation-crosslinked polymer positioned on the metallic surface, wherein the crosslinked polymer comprises:

a radiation crosslinked, polymeric binder of a (meth)acrylate monomer, or (meth)acrylate prepolymer selected from the group consisting of polyfunctional (meth)acrylates, urethane (meth)acrylates, polyester (meth)acrylates, epoxy (meth)acrylates, carbonate (meth)acrylates, polyether (meth)acrylates, and any mixture thereof, and

0.25% to 10% by weight of at least one dithiophosphinic acid of formula HS 2 P(R 1 )(R 2 ) and/or a salt thereof, wherein R 1 and R 2 are, independently of one another, organic radicals with 1 to 20 carbon atoms,

wherein the coating is a chrome-free corrosion control coating, and has a thickness of from 3 to 15 μm.

2. The coating of claim 1 , wherein the polymeric binder is a copolymer of (meth)acrylic acid and one or more comonomers that include an ethylenically unsaturated group and an acidic group.

3. The coating of claim 2 , wherein the one or more comonomers is selected from vinyl acetic acid, crotonic acid, isocrotonic acid, maleic acid, fumaric acid, vinylphosphonic acid, allylphosphonic acid, 3-butenylphosphonic acid, monovinyl phosphate, monoallyl phosphate, mono-3-butenyl phosphate, phosphonoxyethyl (meth)acrylate, or styrenesulfonic acid.

4. The coating of claim 1 , wherein R 1 and R 2 , independently of one another, are selected from methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-dodecyl, 2-ethylhexyl, cyclopentyl, cyclohexyl, phenyl or 4-methylphenyl.

5. The coating of claim 1 , wherein the polymeric binder further includes a polymer selected from the group consisting of poly(meth)acrylates, partially hydrolyzed polyvinyl esters, polyesters, alkyd resins, polylactones, polycarbonates, polyethers, epoxy resin-amine adducts, polyureas, polyamides, polyimides or polyurethanes.

6. The coating of claim 1 , wherein the polymeric binder further includes a polymer selected from polyesters or epoxy resin-amine adducts.

7. The coating of claim 1 , wherein the crosslinked polymer comprises a radiation crosslinked, prepolymer of urethane (meth)acrylates a number-average molar mass M n of from 500 g/mol to 10,000 g/mol, and a (meth)acrylic group content of 2 to 4 mole of (meth)acrylate units per kg of prepolymer.

8. The coating of claim 1 , wherein the at least one dithiophosphinic acid is present from 1% to 6% by weight.

9. The coating of claim 1 , wherein the at least one dithiophosphinic acid is present from 2% to 5% by weight.

10. The coating of claim 9 , wherein the at least one dithiophosphinic acid is selected from di-p-tolyldithiophosphinic acid, diisobutylthiophosphinic acid, dicyclohexylthiophosphinic acid, or the corresponding acid salts thereof.

11. The coating of claim 1 , applied as a coil coating to a surface treated steel coil.

12. An aqueous integrated coating in combination with a metallic surface, the coating comprising a styrene-acrylate dispersion, an anticorrosion pigment based on zinc phosphate, and 0.25% to 10% by weight of at least one dithiophosphinic acid of formula HS 2 P(R 1 )(R 2 ) and/or a salt thereof, wherein R 1 and R 2 are, independently of one another, organic radicals with 1 to 20 carbon atoms,

wherein the integrated coating, and has a thickness of from 40 to 100 μm.

13. The integrated, coating of claim 12 , wherein the at least one dithiophosphinic acid is present from 0.25% to 5% by weight.

14. The integrated coating of claim 12 , wherein the at least one dithiophosphinic acid is an ammonium acid salt.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2017
From: FERNANDEZ GONZALEZ, MONICA; HICKL, MARKUS; MOCK-KNOBLAUCH, CORDULA; ESSIG, MANFRED; SCHREPP, WOLFGANG; BIEHLER, MANFRED
To: BASF AKTIENGESELLSCHAFT
Reel/Frame 042954/0016 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2017
From: BASF SE
To: BASF COATINGS GMBH
Reel/Frame 042955/0159 →
CHANGE OF NAME Recorded Jul 10, 2017
From: BASF AKTIENGESELLSCHAFT
To: BASF SE
Reel/Frame 043140/0537 →
Priority Claims (2)
DE 10 2005 006 233 · Feb 10, 2005 · national
DE 10 2005 046 075 · Sep 26, 2005 · national
Continuity (2)
Continuation 11815792
Related Publication 20160168390A1 · Jun 16, 2016