JP2019537648A5 - - Google Patents
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- JP2019537648A5 JP2019537648A5 JP2019522437A JP2019522437A JP2019537648A5 JP 2019537648 A5 JP2019537648 A5 JP 2019537648A5 JP 2019522437 A JP2019522437 A JP 2019522437A JP 2019522437 A JP2019522437 A JP 2019522437A JP 2019537648 A5 JP2019537648 A5 JP 2019537648A5
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- 239000000203 mixture Substances 0.000 claims description 115
- 239000000178 monomer Substances 0.000 claims description 74
- 229920000642 polymer Polymers 0.000 claims description 57
- 125000000962 organic group Chemical group 0.000 claims description 32
- 150000002148 esters Chemical class 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 26
- 230000002209 hydrophobic effect Effects 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
- 150000001408 amides Chemical class 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 239000004593 Epoxy Substances 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 150000003949 imides Chemical class 0.000 claims description 14
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 14
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 claims description 13
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 12
- 229910052791 calcium Inorganic materials 0.000 claims description 12
- 239000011575 calcium Substances 0.000 claims description 12
- 239000000049 pigment Substances 0.000 claims description 11
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 10
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 10
- 239000011976 maleic acid Substances 0.000 claims description 10
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 10
- 150000007942 carboxylates Chemical class 0.000 claims description 9
- 125000000732 arylene group Chemical group 0.000 claims description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- 125000001072 heteroaryl group Chemical group 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- 125000006588 heterocycloalkylene group Chemical group 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000005549 heteroarylene group Chemical group 0.000 claims description 5
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- -1 ethylene, propylene Chemical group 0.000 claims description 3
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 3
- 150000003568 thioethers Chemical class 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- 150000003009 phosphonic acids Chemical class 0.000 claims description 2
- 150000003460 sulfonic acids Chemical class 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 description 15
- 239000003431 cross linking reagent Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- UJMDYLWCYJJYMO-UHFFFAOYSA-N benzene-1,2,3-tricarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1C(O)=O UJMDYLWCYJJYMO-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 125000003010 ionic group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920005596 polymer binder Polymers 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 229920005603 alternating copolymer Polymers 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662415154P | 2016-10-31 | 2016-10-31 | |
| US62/415,154 | 2016-10-31 | ||
| PCT/US2017/059227 WO2018081780A2 (en) | 2016-10-31 | 2017-10-31 | Polymers for inkjet ink compositions |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020158366A Division JP7114662B2 (ja) | 2016-10-31 | 2020-09-23 | インクジェットインク組成物のためのポリマー |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019537648A JP2019537648A (ja) | 2019-12-26 |
| JP2019537648A5 true JP2019537648A5 (https=) | 2020-11-12 |
| JP7053603B2 JP7053603B2 (ja) | 2022-04-12 |
Family
ID=60543655
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019522437A Active JP7053603B2 (ja) | 2016-10-31 | 2017-10-31 | インクジェットインク組成物のためのポリマー |
| JP2020158366A Active JP7114662B2 (ja) | 2016-10-31 | 2020-09-23 | インクジェットインク組成物のためのポリマー |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020158366A Active JP7114662B2 (ja) | 2016-10-31 | 2020-09-23 | インクジェットインク組成物のためのポリマー |
Country Status (8)
| Country | Link |
|---|---|
| US (4) | US10138388B2 (https=) |
| JP (2) | JP7053603B2 (https=) |
| CN (2) | CN120966314A (https=) |
| DE (2) | DE112017005486B4 (https=) |
| FR (2) | FR3058151B1 (https=) |
| GB (2) | GB2592298B (https=) |
| NL (2) | NL2019837B1 (https=) |
| WO (1) | WO2018081780A2 (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12091560B2 (en) * | 2017-05-30 | 2024-09-17 | Dic Corporation | Ink, printed article, and method of manufacturing printed article |
| JP2021529228A (ja) | 2018-06-27 | 2021-10-28 | インターナショナル イメージング マテリアルズ， インコーポレーテッドＩｎｔｅｒｎａｔｉｏｎａｌ Ｉｍａｇｉｎｇ Ｍａｔｅｒｉａｌｓ， Ｉｎｃ． | 布地インクジェット印刷インク |
| JP7364675B2 (ja) | 2018-11-17 | 2023-10-18 | インターナショナル イメージング マテリアルズ， インコーポレーテッド | 屋外用耐久性インクジェットインク |
| EP3976715A4 (en) * | 2019-05-24 | 2023-10-04 | Coloursmith Labs Inc. | COMPOSITE PARTICLES CONTAINING A HYDROPHOBIC DYE AND AN AMPHIPHILIC BLOCK COPOLYMER AND THEIR USE IN OPTICAL APPLICATIONS |
| KR102196127B1 (ko) * | 2020-03-13 | 2020-12-29 | 한국화학연구원 | 폴리(스티렌-공-말레이미드)계 공중합체 분산제를 포함하는 토너 조성물 및 제조방법 |
| JP7537989B2 (ja) * | 2020-10-26 | 2024-08-21 | 花王株式会社 | インクジェット印刷用水系インク |
| JP7537988B2 (ja) * | 2020-10-26 | 2024-08-21 | 花王株式会社 | インクジェット印刷用水系インク |
| US11413896B2 (en) | 2020-11-18 | 2022-08-16 | International Imaging Materials, Inc. | Digital textile printing inks having zero volatile organic compound solvents therein |
| WO2024069154A1 (en) | 2022-09-26 | 2024-04-04 | Fujifilm Speciality Ink Systems Limited | Printing ink |
| GB202404182D0 (en) | 2024-03-22 | 2024-05-08 | Fujifilm Speciality Ink Systems Ltd | Printing ink |
| GB202404181D0 (en) | 2024-03-22 | 2024-05-08 | Fujifilm Speciality Ink Systems Ltd | Printing ink |
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2017
- 2017-10-31 JP JP2019522437A patent/JP7053603B2/ja active Active
- 2017-10-31 DE DE112017005486.9T patent/DE112017005486B4/de active Active
- 2017-10-31 NL NL2019837A patent/NL2019837B1/en active
- 2017-10-31 CN CN202511183366.1A patent/CN120966314A/zh active Pending
- 2017-10-31 GB GB2020388.1A patent/GB2592298B/en active Active
- 2017-10-31 NL NL2032660A patent/NL2032660B1/en active
- 2017-10-31 GB GB1907585.2A patent/GB2570612B/en active Active
- 2017-10-31 DE DE112017008419.9T patent/DE112017008419B4/de active Active
- 2017-10-31 CN CN201780067698.0A patent/CN109923182A/zh active Pending
- 2017-10-31 FR FR1760269A patent/FR3058151B1/fr active Active
- 2017-10-31 WO PCT/US2017/059227 patent/WO2018081780A2/en not_active Ceased
- 2017-10-31 US US15/798,973 patent/US10138388B2/en active Active
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2018
- 2018-03-21 FR FR1852420A patent/FR3064274B1/fr active Active
- 2018-04-11 US US15/950,718 patent/US10233342B2/en active Active
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2019
- 2019-02-01 US US16/265,139 patent/US20190161631A1/en not_active Abandoned
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2020
- 2020-09-23 JP JP2020158366A patent/JP7114662B2/ja active Active
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2021
- 2021-09-27 US US17/486,153 patent/US20220010152A1/en not_active Abandoned
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