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US4065316A Expired / Lapsed US ⏱️ 0.0 years remaining

Printing ink

Assignee: AT&T Inc
•
Filing: 1976-11-17
•
Granted: 1977-12-27
•
Expires: 1996-11-17
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Abstract

Abstract A printing ink is disclosed. The ink comprises (a) a reactive resin combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28% and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in the resin to the methoxyl substituents is such that in the absence of organic solvent the resin at 25 DEG C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of the resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in the resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: }Molar ratio }Ranges Urea :CH2O :CH3OH CH2O :CH3OH }Lower 1 2.2 1.3 1 1.10 }Upper 1 2.8 2.0 1 2.15 } AND THE RESIN CONSISTING ESSENTIALLY OF <IMAGE> units, -CH2 bridges between the units, and -H, -CH2OH, and -CH2OCH3 substituents; and (b) a pigment.

Inventors

  • 👤 William James Baron
  • 👤 Patrick John Capano

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 12:13
CPC Classifications
C; C09; C09D; C09D11/00; C09D11/02; C09D11/10; C09D11/102

Claims Analysis

Total Claims: 37
Claim 1
Independent Claim 197 words
A printing ink which comprises: a. a resin mixture consisting essentially of an epoxy resin, combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin consisting essentially of ##STR10## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents; and b. a pigment.
Claim 2
Dependent Claim 197 words
A printing ink which comprises: a. a resin mixture consisting essentially of an epoxy resin, combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin consisting essentially of ##STR10## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents; and b. a pigment.
Claim 3
Dependent Claim 57 words
The printing ink as defined in claim 1 wherein in said second resin the molar content of reacted urea, formaldehyde and methanol and the molar ratio of reacted formaldehyde to methanol in the resin is within the range: ______________________________________ Urea mol 1 CH.sub.2 O mols 2.4 CH.sub.3 OH mols 1.5 CH.sub.2 O:CH.sub.3 OH molar ratio 1.60. ______________________________________
Claim 4
Dependent Claim 18 words
The printing ink as defined in claim 1 wherein said second resin is substantially in the dimerictetrameric range.
Claim 5
Dependent Claim 29 words
The printing ink as defined in claim 1 wherein said second resin contains up to about 0.5 mol of C 2 -C 6 alkoxy substituents per urea residue therein.
Claim 6
Dependent Claim 19 words
The printing ink as defined in claim 1 wherein the alkoxy substituents of said second resin comprise n-butoxy substituents.
Claim 7
Dependent Claim 30 words
The printing ink as defined in claim 1 wherein said epoxy resin is selected from the group consisting of a glycidyl polyether of a dihydric phenol and an epoxy novolac.
Claim 8
Dependent Claim 53 words
The printing ink as defined in claim 1 wherein: said epoxy resin is present in said resin mixture in an amount ranging from about 50 to about 90 weight percent, and said pigment is present in the ink in an amount ranging from about 1 to about 35 weight percent of the ink.
Claim 9
Independent Claim 214 words
A method of printing on a surface which comprises: a. applying on the surface an ink comprising (a) a resin mixture consisting essentially of an epoxy resin combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl subtituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin comprising essentially of ##STR11## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents; and (b) a pigment, to form an inked surface.
Claim 10
Independent Claim 214 words
A method of printing on a surface which comprises: a. applying on the surface an ink comprising (a) a resin mixture consisting essentially of an epoxy resin combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl subtituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin comprising essentially of ##STR11## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents; and (b) a pigment, to form an inked surface.
Claim 11
Dependent Claim 20 words
The method as defined in claim 8 which further comprises heat treating said applied ink to cure said applied ink.
Claim 12
Dependent Claim 56 words
The method as defined in claim 8 wherein in said second resin the molar content of reacted urea, formaldehyde and methanol and the molar ratio of reacted formaldehyde to methanol in the resin is within the range: ______________________________________ Urea mol 1 CH.sub.2 O mols 2.4 CH.sub.3 OH mols 1.5 CH.sub.2 O:CH.sub.3 OH molar ratio 1.60. ______________________________________
Claim 13
Dependent Claim 17 words
The method as defined in claim 8 wherein said second resin is substantially in the dimerictetrameric range.
Claim 14
Dependent Claim 28 words
The method as defined in claim 8 wherein said second resin contains up to about 0.5 mol of C 2 -C 6 alkoxy substituents per urea residue therein.
Claim 15
Dependent Claim 18 words
The method as defined in claim 8 wherein the alkoxy substituents of said second resin comprise n-butoxy substituents.
Claim 16
Dependent Claim 29 words
The method as defined in claim 8 wherein said epoxy resin is selected from the group consisting of a glycidyl polyether of a dihydric phenol and an epoxy novolac.
Claim 17
Dependent Claim 52 words
The method as defined in claim 8 wherein: said epoxy resin is present in said resin mixture in an amount ranging from about 50 to about 90 weight percent, and said pigment is present in said ink in an amount ranging from about 1 to about 35 weight percent of said ink.
Claim 18
Independent Claim 213 words
A method of forming a solvent-free printing ink, which comprises: a. forming a liquid resin mixture consisting essentially of an epoxy resin and a second resin, comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin consisting essentially of ##STR12## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents; and b. combining said liquid resin mixture with a pigment to form the ink.
Claim 19
Independent Claim 213 words
A method of forming a solvent-free printing ink, which comprises: a. forming a liquid resin mixture consisting essentially of an epoxy resin and a second resin, comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin consisting essentially of ##STR12## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents; and b. combining said liquid resin mixture with a pigment to form the ink.
Claim 20
Dependent Claim 56 words
The method as defined in claim 16 wherein in said second resin the molar content of reacted urea, formaldehyde and methanol and the molar ratio of reacted formaldehyde to methanol in the resin is within the range: ______________________________________ Urea mol 1 CH.sub.2 O mols 2.4 CH.sub.3 OH mols 1.5 CH.sub.2 O:CH.sub.3 OH molar ratio 1.60. ______________________________________
Claim 21
Dependent Claim 17 words
The method as defined in claim 16 wherein said second resin is substantially in the dimerictetrameric range.
Claim 22
Dependent Claim 28 words
The method as defined in claim 16 wherin said secnd resin contains up to about 0.5 mol of C 2 -C 6 alkoxy substituents per urea residue therein.
Claim 23
Dependent Claim 18 words
The method as defined in claim 16 wherein the alkoxy substituents of said second resin comprise n-butoxy substituents.
Claim 24
Dependent Claim 29 words
The method as defined in claim 16 wherein said epoxy resin is selected from the group consisting of a glycidyl polyether of a dihydric phenol and an epoxy novolac.
Claim 25
Dependent Claim 52 words
The method as defined in claim 16 wherein: said epoxy resin is present in said resin mixture in an amount ranging from about 50 to about 90 weight percent, and said pigment is present in the ink in an amount ranging from about 1 to about 35 weight percent of the ink.
Claim 26
Independent Claim 254 words
A method of selectively depositing a metal on a surface, which comprises: a. sensitizing the surface with a sensitizing species capable of catalyzing a metal deposition from an electroless metal deposition solution; b. selectively coating said sensitized surface with at least a resin coat comprising a reactive resin combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin consisting essentially of ##STR13## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents to delineate an exposed sensitized surface pattern; and c. treating said selectively coated surface with a desensitizing agent to desensitize said exposed pattern and sensitize said resin coat.
Claim 27
Independent Claim 254 words
A method of selectively depositing a metal on a surface, which comprises: a. sensitizing the surface with a sensitizing species capable of catalyzing a metal deposition from an electroless metal deposition solution; b. selectively coating said sensitized surface with at least a resin coat comprising a reactive resin combined with a second resin comprising a substantially anhydrous water-soluble thermosetting stable methylated urea-formaldehyde resin wherein the weight of the methoxyl substituents therein is between 28 and 40% of the weight of the resin and the molar ratio of the reacted formaldehyde in said resin to said methoxyl substituents is such that in the absence of organic solvent the resin at 25° C. is soluble to the extent of at least 50% by weight in water and dissolves at least 50% of its weight of toluene, the polymeric form of said resin being not substantially in excess of tetrameric, the molar ratio of reacted urea to reacted formaldehyde in said resin and the molar ratio of reacted formaldehyde to reacted methanol therein being within the ranges: ______________________________________ Molar ratio Ranges Urea :CH.sub.2 O :CH.sub.3 OH CH.sub.2 O :CH.sub.3 OH ______________________________________ Lower 1 2.2 1.3 1 1.10 Upper 1 2.8 2.0 1 2.15 ______________________________________ and said resin consisting essentially of ##STR13## units, --CH 2 bridges between said units, and --H, --CH 2 OH and --CH 2 OCH 3 substituents to delineate an exposed sensitized surface pattern; and c. treating said selectively coated surface with a desensitizing agent to desensitize said exposed pattern and sensitize said resin coat.
Claim 28
Dependent Claim 33 words
The method as defined in claim 23 which further comprises treating said desensitizing agent treated surface with an electroless metal deposition soluton to selectively deposit an electroless metal on said sensitized resin coat.
Claim 29
Dependent Claim 23 words
The method as defined in claim 23 wherein said desensitizing agent comprises a mixture comprising a phosphate containing compound combined with a base.
Claim 30
Dependent Claim 56 words
The method as defined in claim 23 wherein in said second resin the molar content of reacted urea, formaldehyde and methanol and the molar ratio of reacted formaldehyde to methanol in the resin is within the range: ______________________________________ Urea mol 1 CH.sub.2 O mols 2.4 CH.sub.3 OH mols 1.5 CH.sub.2 O:CH.sub.3 OH molar ratio 1.60. ______________________________________
Claim 31
Dependent Claim 17 words
The method as defined in claim 23 wherein said second resin is substantially in the dimerictetrameric range.
Claim 32
Dependent Claim 28 words
The method as defined in claim 23 wherein said second resin contains up to about 0.5 mol of C 2 -C 6 alkoxy substituents per urea residue therein.
Claim 33
Dependent Claim 18 words
The method as defined in claim 23 wherein the alkoxy substituents of said second resin comprise n-butoxy substituents.
Claim 34
Dependent Claim 15 words
The method as defined in claim 23 wherein said reactive resin comprises an epoxy resin.
Claim 35
Dependent Claim 29 words
The method as defined in claim 30 wherein: said epoxy resin is selected from the group consisting of a glycidyl polyether of a dihydric phenol and an epoxy novolac.
Claim 36
Dependent Claim 21 words
The method as defined in claim 31 wherein: said desensitizing agent comprises a phosphate compound combined with an alkali metal base.
Claim 37
Dependent Claim 29 words
The method as defined in claim 23 wherein said reactive resin is present in said resin mixture in an amount ranging from about 50 to about 90 weight percent.

References Cited (Backward Citations)

US2498454A Cited
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US3532518A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-12-26 1981-06-27 1981-12-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-12-26 1985-06-27 1985-12-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-12-26 1989-06-27 1989-12-27 $7700.00 Window Closed / Lapsed

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