US4822464A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Water-compatible coating resin
Assignee: 3M Co
•
Filing: 1986-09-12
•
Granted: 1989-04-18
•
Expires: 2006-09-12
Abstract
Abstract Water-compatible resins containing a residue of an aryl or cycloalkyl compound having a sufficiently bulky structure to raise the T g of a specified cured epoxy resin by more than 20° C. The resins preferably are used in cathodic electrophoretically-depositable coating compositions.
Inventors
- 👤 Alphonsus V. Pocius
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-04 22:23
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/18; C08G59/40; C08G59/14; C08G59/1433; C08G59/20; C08G59/22; C08G59/32; C08G59/3218; C08G59/50; C08G59/5033; C08G59/62; C08G59/621; C09; C09D; C09D163/00; C09D5/00; C09D5/44; C09D5/4419; C09D5/443; Y; Y10; Y10S; Y10S524/00; Y10S524/901
Claims Analysis
Total Claims: 3
Claim 1
Independent Claim
308 words
A process for coating a metallic substrate with a cathodic electrophoretically depositable structural adhesive bonding primer, comprising the steps of: (A) placing said substrate in fluid contact with an anode and a coating composition comprising (i) water-compatible resin having a substantially linear structure of the formula: A.sup.- + C--E--(L--E).sub.y --C.sup.+ A.sup.- wherein: each E is independently a residue of a diepoxide; each L is independently a residue of an aryl or cycloalkyl linking compound having an average of two epoxide-reactive groups and bulky structure that is sufficiently T g -enhancing to raise by more than 20° C. the T g of a first cured epoxy resin that has been (a) made from the reaction product obtained by combining DGEBA and said linking compound at a 2.1:1 ratio of moles of said DGEBA to moles of said linking compound, (b) cured using piperidine at a 9.08:1 ratio of moles of epoxy groups in said reaction product to moles of said piperidine, and (c) analyzed using dynamic mechanical analysis, when compared to the T g of a second cured epoxy resin made and cured similarly but using bisphenol A in place of said linking compound; each C is independently a cationic water-compatible ammonium, sulfonium or phosphonium group; each A is independently the conjugate base of a water-soluble acid HA having a pK a for use under cathodic electrodeposition conditions; and y has an average value of about 1 to about 20; (ii) crosslinking agent; (iii) water; and (v) resin solvent or coalescing solvent; (B) passing electrical current between said substrata and said anode for a time period sufficiently long to attain a continuous coating of said primer on said substrate; (C) removing excess primer from said substrate; and (D) heating said primer at a curing temperature and for a curing time sufficient to crosslink said primer to a solvent-resistant state.
Claim 2
Dependent Claim
308 words
A process for coating a metallic substrate with a cathodic electrophoretically depositable structural adhesive bonding primer, comprising the steps of: (A) placing said substrate in fluid contact with an anode and a coating composition comprising (i) water-compatible resin having a substantially linear structure of the formula: A.sup.- + C--E--(L--E).sub.y --C.sup.+ A.sup.- wherein: each E is independently a residue of a diepoxide; each L is independently a residue of an aryl or cycloalkyl linking compound having an average of two epoxide-reactive groups and bulky structure that is sufficiently T g -enhancing to raise by more than 20° C. the T g of a first cured epoxy resin that has been (a) made from the reaction product obtained by combining DGEBA and said linking compound at a 2.1:1 ratio of moles of said DGEBA to moles of said linking compound, (b) cured using piperidine at a 9.08:1 ratio of moles of epoxy groups in said reaction product to moles of said piperidine, and (c) analyzed using dynamic mechanical analysis, when compared to the T g of a second cured epoxy resin made and cured similarly but using bisphenol A in place of said linking compound; each C is independently a cationic water-compatible ammonium, sulfonium or phosphonium group; each A is independently the conjugate base of a water-soluble acid HA having a pK a for use under cathodic electrodeposition conditions; and y has an average value of about 1 to about 20; (ii) crosslinking agent; (iii) water; and (v) resin solvent or coalescing solvent; (B) passing electrical current between said substrata and said anode for a time period sufficiently long to attain a continuous coating of said primer on said substrate; (C) removing excess primer from said substrate; and (D) heating said primer at a curing temperature and for a curing time sufficient to crosslink said primer to a solvent-resistant state.
Claim 3
Dependent Claim
46 words
A process according to claim 1, wherein said substrate comprises aluminum, said resin contains nitrogen, said crosslinking agent comprises a bis-maleimide crosslinking film-former or a crosslinking pigment, said curing temperature is about 176° C. or less, and said curing time is about 2 hours or less.
References Cited (Backward Citations)
US2444536A
Cited
US3477990A
Cited
US3663389A
Cited
US3962165A
Cited
US3894922A
Cited
US3935087A
Cited
US4064090A
Cited
US3975250A
Cited
US3959106A
Cited
US4035272A
Cited
US3925181A
Cited
US4110287A
Cited
US4037018A
Cited
US4025409A
Cited
US4130469A
Cited
US4148772A
Cited
US4104147A
Cited
US4029561A
Cited
US4066523A
Cited
US4094843A
Cited
US4134864A
Cited
US4069210A
Cited
US4140816A
Cited
US4246151A
Cited
US4159233A
Cited
US4198331A
Cited
US4248753A
Cited
US4256560A
Cited
US4503266A
Cited
US4274989A
Cited
US4260720A
Cited
US4376848A
Cited
US4315044A
Cited
US4467122A
Cited
US4339369A
Cited
US4396732A
Cited
US4420574A
Cited
US4405427A
Cited
US4593078A
Cited
US4566963A
Cited
US4695508A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1992-04-17 | 1992-10-17 | 1993-04-18 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1996-04-17 | 1996-10-17 | 1997-04-18 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2000-04-17 | 2000-10-17 | 2001-04-18 | $7700.00 | Window Closed / Lapsed |