WO2021198398A1 - Elastic materials prepared from energy-curable liquid compositions - Google Patents

Elastic materials prepared from energy-curable liquid compositions Download PDF

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Publication number
WO2021198398A1
WO2021198398A1 PCT/EP2021/058550 EP2021058550W WO2021198398A1 WO 2021198398 A1 WO2021198398 A1 WO 2021198398A1 EP 2021058550 W EP2021058550 W EP 2021058550W WO 2021198398 A1 WO2021198398 A1 WO 2021198398A1
Authority
WO
WIPO (PCT)
Prior art keywords
meth
acrylate
acrylates
elastic material
component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2021/058550
Other languages
English (en)
French (fr)
Inventor
Zackariah Weinert
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arkema France SA
Original Assignee
Arkema France SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Arkema France SA filed Critical Arkema France SA
Priority to KR1020227037938A priority Critical patent/KR20220162759A/ko
Priority to US17/915,178 priority patent/US20230124643A1/en
Priority to JP2022560098A priority patent/JP2023520232A/ja
Priority to IL296891A priority patent/IL296891A/en
Priority to CN202180039373.8A priority patent/CN115768807A/zh
Priority to EP21714917.8A priority patent/EP4127004A1/en
Publication of WO2021198398A1 publication Critical patent/WO2021198398A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
    • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
    • C08F290/06—Polymers provided for in subclass C08G
    • C08F290/067—Polyurethanes; Polyureas
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/12—Esters of monohydric alcohols or phenols
    • C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
    • C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
    • C08F220/281—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
    • C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
    • C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
    • C08F220/286—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety and containing polyethylene oxide in the alcohol moiety, e.g. methoxy polyethylene glycol (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
    • C08F220/343—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4825—Polyethers containing two hydroxy groups

Definitions

  • a material In order to achieve the resiliency desired in an elastomer, a material must 1) deform under stress and 2) quickly return to its original shape after the stress is removed. In a polymeric material, crosslinking between the polymer chains decreases its ability to deform. Thus, too much crosslinking will preclude any resiliency. On the other hand, crosslinking is required for the material to return to its original shape after the stress is removed. For a given composition, there is a crosslink density that provides optimal resiliency. A material’s elongation is also highly dependent on the crosslink density; crosslinking decreases elongation. The crosslink density required for rebound is enough to severely limit the elongation. For this reason, the defining challenge in formulating an energy-curable composition that is capable of providing an elastic material once cured is simultaneously obtaining high elongation and high resiliency.
  • diol » means a compound bearing two hydroxyl groups.
  • hydroxyl-functionalized (meth)acrylate means a compound comprising one hydroxyl group and at least one (meth)acrylate functional group.
  • amino group » means a -NR ai R bi group, wherein R ai and RM are independently H or an optionally substituted alkyl.
  • aryl » means an aromatic hydrocarbon group.
  • unsaturated compound/group/linker » means a compound/group/linker that comprises a double or triple carbon-carbon bond, in particular a double carbon-carbon bond.
  • the oligomer may contain regions where the structure is similar to that of common elastomeric materials (e.g., polyurethane, polyisoprene, polybutadiene, polyisobutylene) or may contain no structural similarities to conventional elastomers.
  • common elastomeric materials e.g., polyurethane, polyisoprene, polybutadiene, polyisobutylene
  • the polyether polyol may have a number average molecular weight of at least 2,000 Daltons, at least 3,000 Daltons, at least 4,000 Daltons or at least 5,000 Daltons.
  • the ethylenically unsaturated nitrogen-containing monomer may comprise an

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
PCT/EP2021/058550 2020-04-01 2021-04-01 Elastic materials prepared from energy-curable liquid compositions Ceased WO2021198398A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
KR1020227037938A KR20220162759A (ko) 2020-04-01 2021-04-01 에너지-경화 가능한 액체 조성물로부터 제조된 탄성 물질
US17/915,178 US20230124643A1 (en) 2020-04-01 2021-04-01 Elastic materials prepared from energy-curable liquid compositions
JP2022560098A JP2023520232A (ja) 2020-04-01 2021-04-01 エネルギー硬化性液体組成物から調製された弾性材料
IL296891A IL296891A (en) 2020-04-01 2021-04-01 Elastic materials prepared from energy curable liquid compositions
CN202180039373.8A CN115768807A (zh) 2020-04-01 2021-04-01 由能量固化性液体组合物制备的弹性材料
EP21714917.8A EP4127004A1 (en) 2020-04-01 2021-04-01 Elastic materials prepared from energy-curable liquid compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR2003255A FR3108907B1 (fr) 2020-04-01 2020-04-01 Matériaux élastiques préparés à partir de compositions liquides durcissables par énergie
FRFR2003255 2020-04-01

Publications (1)

Publication Number Publication Date
WO2021198398A1 true WO2021198398A1 (en) 2021-10-07

Family

ID=72088215

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2021/058550 Ceased WO2021198398A1 (en) 2020-04-01 2021-04-01 Elastic materials prepared from energy-curable liquid compositions

Country Status (9)

Country Link
US (1) US20230124643A1 (https=)
EP (1) EP4127004A1 (https=)
JP (1) JP2023520232A (https=)
KR (1) KR20220162759A (https=)
CN (1) CN115768807A (https=)
FR (1) FR3108907B1 (https=)
IL (1) IL296891A (https=)
TW (1) TWI832041B (https=)
WO (1) WO2021198398A1 (https=)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2024027876A (ja) * 2022-08-19 2024-03-01 住友ゴム工業株式会社 光硬化性組成物およびこれからなる成形体
WO2024201476A1 (en) * 2023-03-31 2024-10-03 Stratasys Ltd. Formulations usable in additive manufacturing of 3d objects that feature an elastomeric material

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116482943B (zh) * 2023-04-25 2025-10-24 华东师范大学 一种基于对比学习的光刻工艺窗口检测方法
WO2025145319A1 (en) * 2024-01-03 2025-07-10 Henkel Ag & Co. Kgaa Anti-static photocurable adhesive composition

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US5268396A (en) 1990-11-02 1993-12-07 Lai Juey H Organosilicon soft denture liners
EP0982629A1 (en) * 1998-08-28 2000-03-01 Macdermid Incorporated Photosensitive resin composition useful in fabricating printing plates
US6265476B1 (en) 1997-04-08 2001-07-24 Dsm N.V. Radiation-curable binder compositions having high elongation and toughness after cure
US7198576B2 (en) 2003-06-17 2007-04-03 Acushnet Company Golf ball comprising UV-cured non-surface layer
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US20120157564A1 (en) 2009-08-25 2012-06-21 Bridgestone Corporation Energy ray-curable elastomer composition
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KR101892775B1 (ko) * 2011-04-27 2018-08-28 에이지씨 가부시키가이샤 발수발유제 조성물, 그 제조 방법 및 물품
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JP6831333B2 (ja) * 2015-04-02 2021-02-17 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーＥ．Ｉ．Ｄｕ Ｐｏｎｔ Ｄｅ Ｎｅｍｏｕｒｓ Ａｎｄ Ｃｏｍｐａｎｙ ポリマー系グラビア印刷版及び多官能性ウレタンを有する硬化性組成物を用いてそれを製造する方法
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US6265476B1 (en) 1997-04-08 2001-07-24 Dsm N.V. Radiation-curable binder compositions having high elongation and toughness after cure
EP0982629A1 (en) * 1998-08-28 2000-03-01 Macdermid Incorporated Photosensitive resin composition useful in fabricating printing plates
US7198576B2 (en) 2003-06-17 2007-04-03 Acushnet Company Golf ball comprising UV-cured non-surface layer
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2024027876A (ja) * 2022-08-19 2024-03-01 住友ゴム工業株式会社 光硬化性組成物およびこれからなる成形体
WO2024201476A1 (en) * 2023-03-31 2024-10-03 Stratasys Ltd. Formulations usable in additive manufacturing of 3d objects that feature an elastomeric material

Also Published As

Publication number Publication date
CN115768807A (zh) 2023-03-07
FR3108907B1 (fr) 2022-07-08
KR20220162759A (ko) 2022-12-08
EP4127004A1 (en) 2023-02-08
FR3108907A1 (fr) 2021-10-08
TWI832041B (zh) 2024-02-11
US20230124643A1 (en) 2023-04-20
IL296891A (en) 2022-12-01
JP2023520232A (ja) 2023-05-16
TW202146565A (zh) 2021-12-16

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