IP Library Granted Patent US 8,816,012
Granted Patent B2
US 8,816,012 · App. 12/858,623 · Granted Aug 26, 2014

Curable acrylate based printing medium

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Quick Facts
Patent No.
US 8,816,012
App. No.
12/858,623
Granted
Aug 26, 2014
Kind
B2
Abstract

An acrylate-based curable printing medium is disclosed. Acrylates, in the form of monomers, dimers, trimers and oligomers, as well as resins, form an interpenetrating polymer network by crosslinking, which is effected by heat, and optionally peroxide curing agents. Formulations can be tailored to achieve desired properties of the cured polymer including film hardness, burnout properties, and adhesion to glass. Such properties are adjusted by manipulating the relative proportions of the acrylic monomers, oligomers and resins that are used as a ceramic medium or vehicle.

Claims (27)

1. A low VOC, heat-curable medium comprising:

a. 20-95 wt % of heat curable mono-functional acrylate monomers, di-functional acrylate monomers and tri-functional acrylate monomers selected from the group consisting of

i. monofunctional acrylate monomers selected from the group consisting of 2(2-ethoxyethoxy) ethyl acrylate; 2-phenoxyethyl acrylate; isodecyl acrylate; lauryl acrylate; and stearyl acrylate;

ii. difunctional acrylate monomers including at least one of a C 2 -C 22 aliphatic group and a C 6 -C 30 aromatic group, and

iii. trifunctional acrylate monomers including at least one of a C 2 -C 24 aliphatic group and a C 6 -C 36 aromatic group

with the proviso that the heat-curable medium includes at least one monofunctional acrylate monomer;

b. 0.1-20 wt % of a solvent having a boiling point above 150° C. at STP,

c. 0.1-20 wt % of an acrylic resin, and

d. 0.1-18 wt % of an oligomer including a polyester residue and a urethane residue wherein the medium has a viscosity of 40,000 to 150,000 cps when measured at a shear rate of 0.125/second.

2. The medium of claim 1 wherein the oligomer is present in an amount of 0.1-15 wt % of the medium, and wherein the oligomer has a molecular weight of 600 to 1800.

3. The medium of claim 1 , wherein the oligomer is selected from the group consisting of acrylated polyester-urethane copolymers; polyester-urethane copolymers; and combinations thereof.

4. The medium of claim 1 , wherein the curing agent includes a peroxide selected from the group consisting of hydrogen peroxide, sodium peroxide, potassium peroxide, p-anisoyl peroxide, benzoyl peroxide, dibenzoyl peroxide; t-butyl hydroperoxide, t-amyl hydroperoxide, 2,4,-dicumyl α,α′ di(t-butylperoxy)-diisopropyl benzene; 2,5-dimethyl, 2,5-di-(t-butylperoxy) hexane; 2,5-dimethyl, 2,5-di-(t-butylperoxy) hexyne; n-butyl, 4,4-di-(t-butylperoxy)valerate; 1,1-bis-(t-butylperoxy)-3,3,5-trimethyl-cyclohexane; t-butyl perbenzoate, methyl-ethyl ketone peroxide, lauroyl peroxide, and combinations thereof.

5. The medium of claim 1 , further comprising a metal drier.

6. The medium of claim 5 , wherein the metal drier comprises an organometallic compound including a metal selected from the group consisting of iron, copper, manganese, silver, platinum, vanadium, nickel, chromium, palladium, or cobalt, and combinations thereof.

7. The medium of claim 1 , wherein the medium is devoid of photoinitiators.

8. The medium of claim 1 , wherein the medium releases no greater than 140 grams of volatile organic compounds per liter of the medium.

9. The medium of claim 1 , wherein the difunctional acrylate monomers are selected from the group consisting of dipropylene glycol diacrylate; triethylene glycol diacrylate; tripropylene glycol diacrylate; propoxylated neopentyl glycol diacrylate; alkoxylated aliphatic diacrylate and combinations thereof.

10. The medium of claim 1 , wherein the trifunctional acrylate monomers are selected from the group consisting of pentaerythritol triacrylate; ethoxylated 3 trimethylolpropane triacrylate; ethoxylated 20 trimethylolpropane triacrylate; propoxylated 3 trimethylolpropane triacrylate, and combinations thereof.

11. The medium of claim 9 , wherein the trifunctional acrylate monomers are selected from the group consisting of pentaerythritol triacrylate; ethoxylated 3 trimethylolpropane triacrylate; ethoxylated 20 trimethylolpropane triacrylate; propoxylated 3 trimethylolpropane triacrylate, and combinations thereof.

12. The medium of claim 9 , wherein the oligomer is present in an amount of 0.1-15 wt % of the medium, and wherein the oligomer has a molecular weight of 600 to 1800.

13. The medium of claim 9 , wherein the oligomer is an acrylated polyester-urethane copolymer.

14. The medium of claim 9 , wherein the curing agent includes a peroxide selected from the group consisting of hydrogen peroxide, sodium peroxide, potassium peroxide, p-anisoyl peroxide, benzoyl peroxide, dibenzoyl peroxide; t-butyl hydroperoxide, t-amyl hydroperoxide, 2,4,-dicumyl α,α′di(t-butylperoxy)-diisopropyl benzene; 2,5-dimethyl, 2,5-di-(t-butylperoxy) hexane; 2,5-dimethyl, 2,5-di-(t-butylperoxy) hexyne; n-butyl, 4,4-di-(t-butylperoxy)valerate; 1,1-bis-(t-butylperoxy)-3,3,5-trimethyl-cyclohexane; t-butyl perbenzoate, methyl-ethyl ketone peroxide, lauroyl peroxide, and combinations thereof.

15. The medium of claim 9 , further comprising a metal drier.

16. The medium of claim 15 , wherein the metal drier comprises an organometallic compound including a metal selected from the group consisting of iron, copper, manganese, silver, platinum, vanadium, nickel, chromium, palladium, or cobalt, and combinations thereof.

17. The medium of claim 10 , wherein the difunctional acrylate monomers are selected from the group consisting of dipropylene glycol diacrylate; triethylene glycol diacrylate; tripropylene glycol diacrylate; propoxylated neopentyl glycol diacrylate; alkoxylated aliphatic diacrylate and combinations thereof.

18. The medium of claim 2 , wherein the trifunctional acrylate monomers are selected from the group consisting of pentaerythritol triacrylate; ethoxylated 3 trimethylolpropane triacrylate; ethoxylated 20 trimethylolpropane triacrylate; propoxylated 3 trimethylolpropane triacrylate, and combinations thereof.

19. The medium of claim 10 , wherein the oligomer is present in an amount of 0.1-15 wt % of the medium, and wherein the oligomer has a molecular weight of 600 to 1800.

Assignments (5)
SECURITY INTEREST Recorded May 2, 2022
From: CHROMAFLO TECHNOLOGIES CORPORATION; FERRO CORPORATION; FERRO ELECTRONIC MATERIALS INC.; PRINCE ENERGY LLC; PRINCE MINERALS LLC; PRINCE SPECIALTY PRODUCTS LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 059845/0082 →
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT R/F 041736/0178 Recorded Apr 21, 2022
From: PNC BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: FERRO CORPORATION
Reel/Frame 059747/0129 →
SECURITY INTEREST Recorded Feb 16, 2017
From: FERRO CORPORATION
To: PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 041736/0178 →
RELEASE OF SECURITY INTEREST Recorded Feb 15, 2017
From: PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: FERRO CORPORATION
Reel/Frame 041718/0307 →
PATENT SECURITY AGREEMENT Recorded Aug 12, 2014
From: FERRO CORPORATION
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 033522/0966 →