WO2022100927A1 - Cationic epoxy compositions - Google Patents

Cationic epoxy compositions Download PDF

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Publication number
WO2022100927A1
WO2022100927A1 PCT/EP2021/077223 EP2021077223W WO2022100927A1 WO 2022100927 A1 WO2022100927 A1 WO 2022100927A1 EP 2021077223 W EP2021077223 W EP 2021077223W WO 2022100927 A1 WO2022100927 A1 WO 2022100927A1
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WO
WIPO (PCT)
Prior art keywords
epoxy
composition according
salts
present
epoxy composition
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/EP2021/077223
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English (en)
French (fr)
Inventor
Adrian BRANDT
Horst Beck
Alissa BESLER
Sascha POELLER
Johannes Gerardus De Vries
Sarah KIRCHHECKER
Bernhard M. Stadler
Sergey Tin
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to CN202180076989.2A priority Critical patent/CN116438222A/zh
Priority to JP2023528646A priority patent/JP2023549254A/ja
Priority to KR1020237016051A priority patent/KR20230107244A/ko
Publication of WO2022100927A1 publication Critical patent/WO2022100927A1/en
Priority to US18/198,215 priority patent/US20230287168A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • 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
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22—Di-epoxy compounds
    • C08G59/223—Di-epoxy compounds together with monoepoxy compounds
    • 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
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/32—Epoxy compounds containing three or more epoxy groups
    • C08G59/36—Epoxy compounds containing three or more epoxy groups together with mono-epoxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C08K3/36—Silica
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins

Definitions

  • the present invention relates to an epoxy composition
  • an epoxy composition comprising a) a cycloaliphatic epoxy resin; b) a curing agent; and c) a bio-based epoxy compound having a structure I:
  • Adhesive bonds and polymeric coatings are commonly used in the assembly and finishing of manufactured goods. They are used in place of mechanical fasteners, such as screws, bolts and rivets, to provide bonds with reduced machining costs and greater adaptability in the manufacturing process. Adhesive bonds distribute stresses evenly, reduce the possibility of fatigue and seal the joints from corrosive species.
  • Epoxy adhesives consist primarily of epoxy monomers and oligomers and epoxy based reactive diluents. There is a constant need for new chemicals having new technical properties. For example, low odour and low vapor pressure monomers to improve health and safety of a production line and end users.
  • epoxy monomers and oligomers and epoxy based reactive diluents are traditionally produced using petrol-based raw materials.
  • the end users of the epoxy adhesives are now requesting products with increased bio-based content without compromising performance.
  • the present invention relates to an epoxy composition
  • an epoxy composition comprising a) a cycloaliphatic epoxy resin; b) a curing agent; and c) a bio-based epoxy compound having a structure I:
  • the present invention encompasses a cured product of an epoxy composition according the present invention.
  • the present invention relates to use of an epoxy composition according to the present invention as a structural adhesive, a coating, or a primer.
  • the present invention relates to an epoxy composition
  • an epoxy composition comprising a) a cycloaliphatic epoxy resin; b) a curing agent; and c) a bio-based epoxy compound having a structure I:
  • the bio-based epoxy compound I is preferably a p-isomer.
  • the epoxy compound I is synthetised from levulinic acid (LA) as illustrated in schemes 1 - 3 below.
  • Scheme 1 illustrates synthesis of alpha-angelica lactone (a-AL) from levulinic acid (LA) by reactive distillation.
  • p-angelica lactone p-AL
  • a-AL is isomerized to p-AL by using triethyl-amine as a catalyst at 100°C without the use of a solvent.
  • a mixture of p-AL : a-AL - 80:20 is reached after one hour. It has been found that increasing the reaction time does not yield higher p-AL content, because dimerization of the lactones is a competing side reaction.
  • p-AL can be obtained in a yield of up to 37%.
  • the bio-based epoxy compound having a structure I preferably consists of 100% bio-based carbon atoms according ASTM D6866.
  • the bio-based epoxy compound having a structure I may be present in a composition according to the present invention in a quantity of from 1 to 80% by weight based on the total weight of the composition, preferably from 2 to 65%, more preferably from 3 to 45% and even more preferably from 4 to 30%.
  • bio-based epoxy compound having a structure I into an epoxy-based adhesive will provide low viscosity which is ideal for wetting and easier application by dispensing and pumping.
  • low viscosity provides more flexibility to the formulation in form of possibility of using ingredients such as fillers and high viscous resins.
  • the technical data in the example section indicates that use of bio-based epoxy compound having a structure I provides increased flexibility (tensile test) while maintaining Tg in dynamic mechanical analysis and this is good for impact resistance. Further, bio-based epoxy compound having a structure I enables a fast cure and improves wash-off resistance.
  • An epoxy composition according to the present invention comprises a cycloaliphatic epoxy resin.
  • cycloaliphatic epoxy resin is selected from the group consisting of
  • Non-limiting commercially available examples are Celloxide 2021 from Daicel, Araldite CY 170 BD from Huntsman and CER 4221 from Achiewell.
  • a cycloaliphatic epoxy resin may be present in an epoxy composition according to the present invention in a quantity of from 10 to 98% by weight based on the total weight of the composition, preferably from 12 to 85%, more preferably from 15 to 80% and even more preferably from 15 to 60%.
  • the epoxy composition according to the present invention may comprise an additional resin used in a combination with a cycloaliphatic epoxy resin.
  • Suitable additional resins for use in the present invention are for example aliphatic epoxy resins, aromatic epoxy resins, oxetane resins, vinyl ether resins and mixtures thereof.
  • An additional resin may be present in an epoxy composition according to the present invention in a quantity of from 1 to 60% by weight based on the total weight of the composition, preferably from 10 to 50%, more preferably from 20 to 30%.
  • the composition according to the present invention comprises a curing agent, which is preferably a cationic curing agent.
  • a curing agent is selected from the group consisting of ammonium salts; pyridinium salts; imidazolium salts; guadinium salts; oxazolium salts; thiazolium salts; iodinium salts; sulfonium salts; and, phosphonium salts, and mixtures thereof.
  • a hard cation non-nucleophilic anion curing agent may be used.
  • curing agents include salts of lithium and metals from Group II of the Periodic Table, and non-nucleophilic acid.
  • non-nucleophilic acids have a pH of less than 1.0 when measured as a 10% by weight solution in water.
  • the Group II metal salts include calcium and magnesium.
  • non-nucleophilic acids include perchloric, fluoroboric, fluoroarsenic, fluoroantimonic and fluorophosphoric acids.
  • suitable curing agents to be used in the present invention are metal fluoro bo rates; bis(perfluoroalkyl sulfonyl)methane metal salts; aryl diazonium compounds; aromatic iodonium complex salts; aryl iodonium salts; aromatic onium salts of Group la elements; aromatic onium salts of Group Va elements; dicarbonyl chelates of Group Illa-Va elements; onium salts of Group Vlb elements in an MF6 anion where M is selected from phosphorous, antimony and arsenic arylsulfonium salts; aromatic sulfonium complex salts; bis(4- (diphenylsulfonio)-phenyl)sulfide-bis- hexafluorometallic salts such as the phosphate, arsenate, and antimonate salts; aryl sulfonium complex salts of Group II, V and VI elements; aromatic sulf
  • the cationic curing agent may comprise one, mixture of two or mixture of two or more above mentioned salts.
  • Non-limiting commercially available examples of curing agents are K-Pure CXC-1612 and CXC 1821 from King Industries, SP-150, SP-170 and SP-171 from Adeka, Irgacure 250, 270 and PAG 290 from BASF.
  • a curing agent may be present in an epoxy composition according to the present invention in a quantity of from 0.01 to 15% by weight based on the total weight of the composition, preferably from 0.1 to 10%, more preferably from 0.2 to 10% and even more preferably from 0.25 to 5%.
  • An epoxy composition according to the present invention may further comprise an inorganic filler.
  • said inorganic filler is selected from the group consisting of silica, fumed silica, diatomaceous earth, alumina, zinc oxide, iron oxide, magnesium oxide, tin oxide, titanium oxide, magnesium hydroxide, aluminium hydroxide, magnesium carbonate, barium sulphate, gypsum, calcium silicate, talc, glass bead, sericite activated white earth, bentonite, aluminium nitride, silicon nitride, magnesia dihydroxide, alumina trihydroxide, bariumsulfat, chalk, wollastonites and mixtures thereof.
  • Non-limiting commercially available examples are HDK H13L from Wacker and TS720, Ultrabond 5760 and Ultrabond 5780 from Cabot.
  • An inorganic filler may be present in an epoxy composition according to the present invention in a quantity of from 0.1 to 80% by weight based on the total weight of the composition, preferably from 5 to 65%, more preferably from 10 to 55% and even more preferably from 20 to 40%.
  • An epoxy composition according to the present invention may further comprise a toughener.
  • a toughener In general, any toughener can be used in the composition according to the present invention.
  • Suitable tougheners to be used in the present invention are for examples (non-limiting examples)
  • polystyrene resin • OH or acid terminated polyols such as polyethers (PEG, PPG, PTHF and Velvetol) and polyesters (polyester polyols, polyester diols, fatty acid modified bisphenol A diglycidyl ether);
  • core shell particles such as PMMA shell and styrene-polybutadiene core or polybutadiene core or polysiloxane core
  • non-reactive toughener rubbery materials and fillers such as capped elastomeric urethanes, block copolymer rubbers such as styrene-butadiene-isoprene based block copolymers, styrene-isoprene-styrene block copolymers and other rubbery block-copolymers;
  • reactive-toughener rubbery materials such as liquid rubbers with two or more epoxy-reactive groups (e.g. amine-, OH- and acid-terminated) such as butadiene-acrylonitrile-based rubbers, carboxyl-terminated butadiene-acrylonitrile (CTBN) with different contents of acrylonitrile (AN), amino-terminated butadiene-acrylonitrile (ATBN), epoxy-terminated butadiene-acrylonitrile (ETBN), and vinyl-terminated butadiene-acrylonitrile (VTBN); OH- terminated polyether polyols (PEG, PPG, PTHF type, 1.3-propane diol-based), OH- terminated polyethers based on cashew nut shell liquid, OH- or acid-terminated polyesters, OH-terminated thermoplastic polyurethanes, HTPB (hydroxyl-terminated polybutadiene), epoxidized HTPB, polyfarnesene based polyols,
  • inorganic fillers and reinforcing agents that can also act as toughener such as calcium carbonate, barium sulfate, calcium oxide, talc, carbon black, textile fibers, glass particles or fibers, aramid pulp, boron fibers, carbon fibers, mineral silicates, mica, powdered quartz, hydrated aluminum oxide, bentonite, various alumina-silicates including clays such as wollastonite and kaolin, fumed silica, silica aerogel, polyurea compounds, polyamide compounds and metal powders such as aluminum powder or iron powder;
  • toughener such as calcium carbonate, barium sulfate, calcium oxide, talc, carbon black, textile fibers, glass particles or fibers, aramid pulp, boron fibers, carbon fibers, mineral silicates, mica, powdered quartz, hydrated aluminum oxide, bentonite, various alumina-silicates including clays such as wollastonite and kaolin, fumed silica, silic
  • bio-based tougheners that reduce Tg and increase flexibility
  • cardanol based tougheners OH-terminated and epoxy terminated
  • bio-based polyether polyol OH-terminated and epoxy terminated
  • polyfarnesene polyol OH-terminated and epoxy terminated
  • TPUs made from bio-based polyols
  • croda-B toughener polyyester with epoxy termination
  • said toughener is selected from the group consisting of core shell rubber particles, liquid rubbers with two or more epoxy-reactive groups, OH- terminated polyether polyols, OH-terminated thermoplastic polyurethanes, OH-terminated polyethers, polyether urethanes, polyether rubber modified epoxy resins, fatty acid modified epoxy resins, polyether amine epoxy resins, rubber particles, styrene-butadiene-isoprene based block copolymers, polytetrahydrofuran-based toughener, cardolite toughener (PEG or EO modified Cardanol or glycidyl modified cardanol dimer (two epoxies)), polyfarnesene polyol, capped elastomeric urethanes, block copolymer rubbers, epoxy-capped elastomeric polyethers, epoxy-capped elastomeric polyesters, inorganic fillers, reinforcing agents and mixtures thereof.
  • core shell rubber particles
  • Example of commercially available toughener include but is not limited to Kane Ace MX153 from Kaneka.
  • a toughener may be present in an epoxy composition according to the present invention in a quantity of from 0.1 to 50% by weight based on the total weight of the composition, preferably from 5 to 45%, more preferably from 10 to 40% and even more preferably from 20 to 40%.
  • the applicant has found the above ranges suitable for the composition according to the present invention. Too high toughener quantities may lead to poor adhesion properties, poor Tg value and undesired viscosity, whereas too low quantity may lead to a brittle system which is no longer applicable.
  • An epoxy composition according to the present invention may further comprise a reactive diluent.
  • Suitable diluents for use in the present invention are for example methyl ethyl ketone (MEK), dimethylformamide (DMF), ethyl alcohol, propylene glycol methyl ether, propylene glycol methyl ether acetate, dibutyl phthalate, dioctyl phthalate, styrene, low molecular weight polystyrene, styrene oxide, allyl glycidyl ether, phenyl glycidyl ether, butyl glycidyl ether, vinylcyclohexene oxide, neopentylglycol diglycidyl ether, butanediol diglycidyl ether, hexanediol diglycidyl ether, diethylene glycol diglycidyl ether, dipropylene glycol diglycidy
  • Examples of commercially available reactive diluents include but are not limited to DER 732, DER 736 from Palmer Holland, Cardura E10P from Exion and Efka 5381 from BASF.
  • a reactive diluent may be present in an epoxy composition according to the present invention in a quantity of from 0.2 to 15% by weight based on the total weight of the composition, preferably from 0.1 to 7.5%.
  • An adhesion promoter may be added to an epoxy composition according to the present invention to improve the adhesion of the epoxy resin to a substrate.
  • Adhesion promoters may function by forming a new layer at the interface which binds strongly to both the substrate and the coating.
  • the resultant interfacial region may also be more resistant to chemical attack from the environment.
  • adhesion promoter may be determined by the type of surface to which the composition will be applied. That said, the most common commercial adhesion promoters are organosilanes of which certain epoxy functional organosilanes types have been mentioned hereinbefore. Further types of adhesion promoter which may find utility herein include: organometallic compounds such as titanates and zirconates, of which specific examples include isopropyl tri(N-ethylaminoethylamino)titanate, tetraisopropyl di(dioctylphosphito)titanate, neoalkoxytrisneodecanoyl zirconate and zirconium propionate; dihydric phenolic compounds such as catechol and thiodiphenol; polyhydric phenols such as pyrogallol, gallic acid, or tannic acid; phosphoric acid esters such as tricresylphosphate and, plastisols, which are
  • adhesion promoters examples include but are not limited to Glymo from Evonik and Silquest from Momentive.
  • An adhesion promoter may be present in an epoxy composition according to the present invention in a quantity of from 0.01 to 5% by weight based on the total weight of the composition, preferably from 0.1 to 2.5%.
  • An epoxy composition according to the present invention may further comprise an electrically conductive filler.
  • electrically conductive filler is selected from the group consisting of silver, nickel, carbon, carbon black, graphite, graphene, copper, gold, platinum, aluminium, iron, zinc, cobalt, lead, tin alloys, silver coated copper, silver coated graphite, silver coated polymers, silver coated aluminium, silver coated glass, silver coated carbon, silver coated boron nitride, silver coated aluminium oxide, silver coated aluminium hydroxide and mixtures thereof.
  • An electrically conductive filler may be present in an epoxy composition according to the present invention in a quantity of from 20 to 90% by weight based on the total weight of the composition, preferably from 30 to 70% and more preferably from 40 to 60%.
  • An epoxy composition according to the present invention may further comprise a thermal conductor.
  • thermal conductor is selected from the group consisting of alumina, alumina trihydroxide, boron nitride, aluminium nitride, and mixtures thereof. Equally some of the above mentioned electrically conductive fillers may be also used as thermal conductors.
  • Example of commercially available thermal conductor include but is not limited to Polartherm PT110 from Momentive.
  • a thermal conductor may be present in an epoxy composition according to the present invention in a quantity of from 0.01 to 5% by weight based on the total weight of the composition, preferably from 0.2 to 2.5%.
  • An epoxy composition according to the present invention may further comprise a wetting agent.
  • a wetting agent Any wetting agent compatible with epoxy resins may be used.
  • wetting agent is siloxane based wetting agent.
  • examples of commercially available wetting agent include but are not limited to Dynol 980 from Evonik and BYK W 9010, BYK W 940 from BYK.
  • a wetting agent may be present in an epoxy composition according to the present invention in a quantity of from 0.01 to 10% by weight based on the total weight of the composition, preferably from 0.1 to 5%, more preferably from 0.1 to 1.0%.
  • the present invention relates to a cured product of an epoxy composition according to the present invention.
  • the epoxy composition according to the present invention is preferably cured under following conditions two days at 23°C and 50% rh or 30 minutes at 80°C.
  • the present invention encompasses use of an epoxy composition according to the present invention as a structural adhesive, a coating or a primer.
  • the epoxy composition according to the present invention is especially useful for applications where low viscosity is required for easy dispensing and wetting.
  • Lap shear adhesion on steel is measured according to DIN EN ISO 527-1/-2.
  • Pretreatment specimen cleaning with ethyl acetate
  • Pretreatment forms drying for 30min at 80°C

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Epoxy Resins (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Paints Or Removers (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
PCT/EP2021/077223 2020-11-16 2021-10-04 Cationic epoxy compositions Ceased WO2022100927A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CN202180076989.2A CN116438222A (zh) 2020-11-16 2021-10-04 阳离子环氧组合物
JP2023528646A JP2023549254A (ja) 2020-11-16 2021-10-04 カチオン性エポキシ組成物
KR1020237016051A KR20230107244A (ko) 2020-11-16 2021-10-04 양이온성 에폭시 조성물
US18/198,215 US20230287168A1 (en) 2020-11-16 2023-05-16 Cationic epoxy compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP20207701.2 2020-11-16
EP20207701.2A EP4001338B1 (en) 2020-11-16 2020-11-16 Cationic epoxy compositions

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US18/198,215 Continuation US20230287168A1 (en) 2020-11-16 2023-05-16 Cationic epoxy compositions

Publications (1)

Publication Number Publication Date
WO2022100927A1 true WO2022100927A1 (en) 2022-05-19

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Application Number Title Priority Date Filing Date
PCT/EP2021/077223 Ceased WO2022100927A1 (en) 2020-11-16 2021-10-04 Cationic epoxy compositions

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US (1) US20230287168A1 (https=)
EP (1) EP4001338B1 (https=)
JP (1) JP2023549254A (https=)
KR (1) KR20230107244A (https=)
CN (1) CN116438222A (https=)
ES (1) ES2973297T3 (https=)
TW (1) TW202227579A (https=)
WO (1) WO2022100927A1 (https=)

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KR20250026050A (ko) 2023-08-16 2025-02-25 주식회사 케이엠더블유 필터 구조체

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020212149A1 (en) * 2019-04-16 2020-10-22 Henkel Ag & Co. Kgaa Use of functionalized alpha-angelica lactones

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JP4276407B2 (ja) * 2002-05-08 2009-06-10 ヘンケル コーポレイション 光カチオン硬化型エポキシ樹脂組成物
DE102013018088B4 (de) * 2013-02-10 2017-01-26 Karim El Kudsi Beschichtungen auf Epoxydharzbasis und ein Verfahren zu ihrer Herstellung und ihre Verwendungen
ES2736398T3 (es) * 2015-07-02 2019-12-30 Huntsman Adv Mat Licensing Switzerland Gmbh Una composición de resina epoxi termoendurecible para la preparación de artículos de exterior y artículos obtenidos a partir de los mismos
AT521316A1 (de) * 2018-06-07 2019-12-15 All Bones Gmbh Polymermischung sowie deren Verwendung im 3D-Druck
CN110804161B (zh) * 2019-11-20 2022-03-08 长春工业大学 低粘度生物基环氧树脂组合物及碳纤维复合材料

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WO2020212149A1 (en) * 2019-04-16 2020-10-22 Henkel Ag & Co. Kgaa Use of functionalized alpha-angelica lactones

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Title
MIYAGAWA H ET AL: "FRACTURE TOUGHNESS AND IMPACT STRENGTH OF ANHYDRIDE-CURED BIOBASED EPOXY", POLYMER ENGINEERING AND SCIENCE, BROOKFIELD CENTER, US, vol. 45, no. 4, 1 April 2005 (2005-04-01), pages 487 - 495, XP001227904, ISSN: 0032-3888, DOI: 10.1002/PEN.20290 *
ORTUNO R M ET AL: "Beta- Angelica Lactone Epoxide: Chemical Behaviour and some synthetic applications", JOURNAL OF HETEROCYCLIC CHEMISTRY,, vol. 24, 1 January 1987 (1987-01-01), pages 79 - 84, XP002802610 *
ORTUNO R M ET AL: "Enantiomeric @b-angelica lactone epoxides: their syntheses from suitable chiral precursors and their use in the preparation of blastmycinone", TETRAHEDRON, ELSEVIER SIENCE PUBLISHERS, AMSTERDAM, NL, vol. 43, no. 9, 1 January 1987 (1987-01-01), pages 2191 - 2198, XP026596471, ISSN: 0040-4020, [retrieved on 19870101], DOI: 10.1016/S0040-4020(01)86801-0 *

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JP2023549254A (ja) 2023-11-22
ES2973297T3 (es) 2024-06-19
EP4001338B1 (en) 2024-01-31
TW202227579A (zh) 2022-07-16
US20230287168A1 (en) 2023-09-14
EP4001338A1 (en) 2022-05-25
KR20230107244A (ko) 2023-07-14
CN116438222A (zh) 2023-07-14

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