IP Library › Granted Patent US 12,473,449
Granted Patent B2
US 12,473,449 · App. 17/852,351 · Granted Nov 18, 2025

Ink set, image recording method, image recorded article, and three-dimensional article and method for producing the same

Inventors: Kohei Takeshita (Kanagawa, JP); Kazuo Kamohara (Kanagawa, JP)
Assignee: FUJIFILM Corporation
C09D11/38B29C43/10B41M5/0023B41M7/0081C09D11/037C09D11/101C09D11/107C09D11/322C09D11/40C08F2/50C08K3/013
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Quick Facts
Patent No.
US 12,473,449
App. No.
17/852,351
Granted
Nov 18, 2025
Kind
B2
Abstract

Provided are an ink set including a first ink including an ethylenic unsaturated compound and a photopolymerization initiator, the first ink not including a colorant or including a white colorant, and a second ink including an ethylenic unsaturated compound, a photopolymerization initiator, and a colorant, wherein the proportion of the amount of a monofunctional monomer to the total amount of the ethylenic unsaturated compound included in the first ink is 95.0% by mass or more, the proportion of the amount of a monofunctional monomer to the total amount of the ethylenic unsaturated compound included in the second ink is 95.0% by mass or more, and, when the static surface tension of the first ink at 25° C. is defined as T1 and the static surface tension of the second ink at 25° C. is defined as T2, the value calculated by subtracting T1 from T2 is 1 mN/m or more, and applications of the ink set.

Claims (43)

1 . An ink set comprising:

a first ink including an ethylenic unsaturated compound and a photopolymerization initiator, the first ink not including a colorant or including a white colorant; and

a second ink including an ethylenic unsaturated compound, a photopolymerization initiator, and a colorant,

wherein the ethylenic unsaturated compound included in the first ink includes:

a monofunctional monomer that is a compound including one ethylenic unsaturated group, and a proportion of an amount of the monofunctional monomer to a total amount of the ethylenic unsaturated compound included in the first ink is 95.0% by mass or more; and

a silicone compound having an ethylenic unsaturated group,

wherein the ethylenic unsaturated compound included in the second ink includes:

a monofunctional monomer that is a compound including one ethylenic unsaturated group, and a proportion of an amount of the monofunctional monomer to a total amount of the ethylenic unsaturated compound included in the second ink is 95.0% by mass or more; and

a silicone compound having an ethylenic unsaturated group, and

wherein, when a static surface tension of the first ink at 25° C. is defined as T1 and a static surface tension of the second ink at 25° C. is defined as T2, a value calculated by subtracting T1 from T2 is 1 mN/m or more.

2 . The ink set according to claim 1 ,

wherein the value calculated by subtracting T1 from T2 is 1 to 15 mN/m.

3 . The ink set according to claim 1 ,

wherein the value calculated by subtracting T1 from T2 is 2 to 10 mN/m.

4 . The ink set according to claim 1 ,

wherein the monofunctional monomer included in the first ink includes a compound represented by Formula (A) below, and a proportion of an amount of the compound represented by Formula (A) to the total amount of the ethylenic unsaturated compound included in the first ink is 5.0% by mass or more,

wherein the monofunctional monomer included in the second ink includes a compound represented by Formula (A) below, and a proportion of an amount of the compound represented by Formula (A) to the total amount of the ethylenic unsaturated compound included in the second ink is 5.0% by mass or more, and

wherein, in Formula (A), n represents an integer of 2 to 6.

5 . The ink set according to claim 1 ,

wherein, when a viscosity of the first ink at 25° C. is defined as V1 and a viscosity of the second ink at 25° C. is defined as V2, a ratio of V1 to V2 is 2.0 to 20.0.

6 . The ink set according to claim 1 ,

wherein a content of a thioxanthone compound in the first ink is 0.8% by mass or less of a total amount of the first ink.

7 . An image recording method in which the ink set according to claim 1 is used, the method comprising:

a first application step of applying the first ink to an impermeable substrate;

a first irradiation step of irradiating the first ink deposited on the impermeable substrate with a first active energy ray at an irradiation dose of 1 to 50 mJ/cm 2 ;

a second application step of applying the second ink to the first ink irradiated with the first active energy ray; and

a second irradiation step of irradiating the second ink deposited on the impermeable substrate and the first ink irradiated with the first active energy ray with a second active energy ray at an irradiation dose of 100 mJ/cm 2 or more.

8 . A method for producing a three-dimensional article, the method comprising:

a step of producing an image recorded article including the impermeable substrate and an image by the image recording method according to claim 7 ; and

a step of subjecting the image recorded article to vacuum forming to produce a three-dimensional article.

9 . An image recorded article comprising:

an impermeable substrate; and

an image recorded using the ink set according to claim 1 ,

wherein the image includes a first layer that is a cured product of the first ink and a second layer that is a cured product of the second ink, and

wherein the impermeable substrate, the first layer, and the second layer are arranged in this order.

10 . A three-dimensional article that is an article produced by subjecting the image recorded article according to claim 9 to vacuum forming.

11 . An ink set comprising:

a first ink including an ethylenic unsaturated compound and a photopolymerization initiator, the first ink not including a colorant or including a white colorant; and

a second ink including an ethylenic unsaturated compound, a photopolymerization initiator, and a colorant,

wherein the ethylenic unsaturated compound included in the first ink includes a monofunctional monomer that is a compound including one ethylenic unsaturated group, and a proportion of an amount of the monofunctional monomer to a total amount of the ethylenic unsaturated compound included in the first ink is 95.0% by mass or more,

wherein the ethylenic unsaturated compound included in the second ink includes a monofunctional monomer that is a compound including one ethylenic unsaturated group, and a proportion of an amount of the monofunctional monomer to a total amount of the ethylenic unsaturated compound included in the second ink is 95.0% by mass or more,

wherein, when a static surface tension of the first ink at 25° C. is defined as T1 and a static surface tension of the second ink at 25° C. is defined as T2, a value calculated by subtracting T1 from T2 is 1 mN/m or more, and

wherein, when a viscosity of the first ink at 25° C. is defined as V1 and a viscosity of the second ink at 25° C. is defined as V2, a ratio of V1 to V2 is 2.0 to 20.0.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2022
From: TAKESHITA, KOHEI; KAMOHARA, KAZUO
To: FUJIFILM CORPORATION
Reel/Frame 060360/0827 →
Priority Claims (1)
JP 2020-003887 · Jan 14, 2020 · national
Continuity (2)
Continuation PCTJP2020043092 · Nov 18, 2020
Related Publication 20220348779A1 · Nov 3, 2022
References Cited (64)
US 7713462B2 · Hayata · 2010 [cited by examiner]
US 8518169B2 · Oyanagi · 2013 [cited by examiner]
US 8562123B2 · Hayata · 2013 [cited by examiner]
US 8608305B2 · Hayata · 2013 [cited by examiner]
US 8664297B2 · Fujii · 2014 [cited by applicant]
US 8752950B2 · Hayata · 2014 [cited by examiner]
US 8807728B2 · Hayata · 2014 [cited by examiner]
US 8940813B2 · Araki · 2015 [cited by examiner]
US 9010914B2 · Hayata · 2015 [cited by examiner]
US 9139748B2 · Mizutani · 2015 [cited by examiner]
US 9243154B2 · Nakano · 2016 [cited by examiner]
US 9598591B2 · Mizutani · 2017 [cited by examiner]
US 9713926B2 · Nakano · 2017 [cited by examiner]
US 9783696B2 · Steert · 2017 [cited by examiner]
US 10245852B2 · Nakano · 2019 [cited by examiner]
US 10472532B2 · Okamoto · 2019 [cited by examiner]
US 10550275B2 · Hirose · 2020 [cited by examiner]
US 10780717B2 · Nakano · 2020 [cited by examiner]
US 11034165B2 · Sato · 2021 [cited by examiner]
US 11059304B2 · Nakano · 2021 [cited by examiner]
US 11247481B2 · Matsumoto et al. · 2022 [cited by applicant]
US 11332629B2 · Kobayashi · 2022 [cited by examiner]
US 11549028B2 · Matsumoto et al. · 2023 [cited by applicant]
US 11884079B2 · Nakano · 2024 [cited by examiner]
US 20060189712A1 · Kondo · 2006 [cited by applicant]
US 20090155484A1 · Nakamura et al. · 2009 [cited by applicant]
US 20090202795A1 · Hayata et al. · 2009 [cited by applicant]
US 20130260092A1 · Araki et al. · 2013 [cited by applicant]
US 20130295342A1 · Araki et al. · 2013 [cited by applicant]
US 20140370214A1 · Araki et al. · 2014 [cited by applicant]
US 20150353751A1 · Umebayashi · 2015 [cited by applicant]
CN 102993827 · 2013 [cited by applicant]
CN 104228382 · 2014 [cited by applicant]
CN 104937049 · 2015 [cited by applicant]
CN 109328142 · 2019 [cited by applicant]
EP 1911817 · 2008 [cited by applicant]
EP 1967556 · 2008 [cited by applicant]
EP 2230285 · 2010 [cited by applicant]
EP 2484729 · 2012 [cited by applicant]
EP 2650338A2 · 2013 [cited by examiner]
EP 2853367 · 2015 [cited by applicant]
EP 2966133 · 2016 [cited by applicant]
EP 3608373 · 2020 [cited by applicant]
JP 2004285217 · 2004 [cited by applicant]
JP 2008100501 · 2008 [cited by applicant]
JP 2009144057 · 2009 [cited by applicant]
JP 2009185186 · 2009 [cited by applicant]
JP 2010137445 · 2010 [cited by applicant]
JP 2010137445A · 2010 [cited by examiner]
JP 2012177072 · 2012 [cited by applicant]
JP 2013227515 · 2013 [cited by applicant]
JP 5606567 · 2014 [cited by applicant]
JP 2019044174A · 2019 [cited by examiner]
JP 6735011B1 · 2020 [cited by examiner]
WO 2006087930 · 2006 [cited by applicant]
WO 2015049873 · 2015 [cited by applicant]
WO 2019131215 · 2019 [cited by applicant]
Office Action of China Counterpart Application, with English translation thereof, issued on Dec. 26, 2022, pp. 1-28. [cited by applicant]
“International Search Report (Form PCT/ISA/210) of PCT/JP2020/043092,” mailed on Jan. 26, 2021, with English translation thereof, pp. 1-5. [cited by applicant]
“Written Opinion of the International Searching Authority (Form PCT/ISA/237)” of PCT/JP2020/043092, mailed on Jan. 26, 2021, with English translation thereof, pp. 1-8. [cited by applicant]
Office Action of Japan Counterpart Application, with English translation thereof, issued on Apr. 18, 2023, pp. 1-5. [cited by applicant]
“Notice of Reasons for Rejection of China Counterpart Application”, issued on Jul. 18, 2023, with English translation thereof, p. 1-p. 28. [cited by applicant]
“Search Report of Europe Counterpart Application”, issued on May 22, 2023, p. 1-p. 8. [cited by applicant]
“Final Office Action of China Counterpart Application”, issued on Oct. 24, 2023, with English translation thereof, pp. 1-20. [cited by applicant]