F-Term-List

C08G59/00-59/72

AA00
COMPOUND HAVING MORE THAN ONE EPOXY GROUPS IN THE MOLECULE, I.E. EPOXY RESIN

AA01

AA02

AA04

AA05

AA06

. Epoxy resins in general i.e. polyvalent epoxy compounds

. . Polyhydric phenol based epoxy resins in general

. using a plurality of epoxy resins

. . two kinds

. . three kinds

AB00
EPOXY RESIN OBTAINED FROM LOW MOLECULAR WEIGHT POLYHYDROXY COMPOUND OTHER THAN PHENOLS AND EPIHALOHYDRINS

AB01

AB02

AB03

AB05

AB06

AB07

AB08

AB09

AB10

. having two hydroxy groups

. having three hydroxy groups

. having four or more hydroxy groups

. containing halogens

. containing carbon-to-carbon double bonds

. containing alicyclic groups

. containing oxygen other than hydroxy groups

. . containing ether groups (-O-)

. . . containing polyether sequences ((-R-O-)n n=2-9)

AB11

AB12

AB13

AB14

AB15

AB16

AB17

AB18

AB19

AB20

. . containing oxygen-containing hetero rings

. containing nitrogen

. . containing nitrogen-containing hetero rings

. . . Imide rings

. . . Hydantoin rings

. . . Triazine rings

. . . . Triglycidylisocyanurates

. containing sulfur

. containing phosphorus

. containing other atoms than carbon hydrogen oxygen nitrogen sulfur phosphorus or halogens

AC00
EPOXY RESIN OBTAINED FROM LOW MOLECULAR WEIGHT POLYPHENOLS OTHER THAN BISPHENOL AND EPIHALOHYDRIN

AC01

AC02

AC03

AC05

AC06

AC07

AC08

AC09

AC10

. having two phenolic OH groups

. having three phenolic OH groups

. having four or more phenolic OH groups

. having a plurality of phenolic OH groups in one nucleus

. containing halogens

. containing carbon-to-carbon double bonds

. containing alicyclic groups

. containing oxygen other than phenolic OH groups

. . containing OH groups

AC11

AC12

AC13

AC14

AC15

AC16

AC17

AC18

AC19

AC20

. . containing ether groups (-O-)

. . . containing polyether sequences ((-R-O-)n n=2-9)

. . containing oxygen-containing hetero rings

. containing nitrogen

. . containing nitrogen-containing hetero rings

. . . Imide rings

. . . Hydantoin rings

. . . Triazine rings

. containing sulfur

. containing phosphorus

AC21

. containing other atoms than carbon hydrogen oxygen nitrogen sulfur phosphorus or halogens

AD00
EPOXY RESIN OBTAINED FROM BISPHENOL AND EPIHALOHYDRINS

AD01

AD03

AD04

AD05

AD07

AD08

AD09

AD10

. Bisphenol glycidyl ether based epoxy resins in general

. having substituents in phenol nucleus

. . Alkyl groups

. . Halogen-containing groups

. (X) being single bonds

. (X) being aliphatic groups e.g. bisphenols A or F

. . containing halogens

. . containing carbon-to-carbon double bonds

AD11

AD12

AD13

AD14

AD15

AD16

AD17

AD18

AD19

AD20

. (X) being alicyclic groups

. (X) being aromatic groups

. (X) being oxygen-containing groups e.g. keto groups or ester groups

. . containing OH groups

. . containing ether groups (-O-)

. . Oxygen-containing hetero rings e.g. spiroacetals

. (X) being nitrogen-containing groups

. . Nitrogen-containing hetero rings

. . . Imide rings

. (X) being sulfur-containing groups

AD21

AD22

AD23

. . containing sulfone groups (-SO2-) e.g. bisphenols S

. (X) being phosphorus-containing groups

. (X) being atoms other than carbon hydrogen oxygen nitrogen sulfur phosphorus or halogens

AE00
EPOXY RESIN OBTAINED FROM MACROMOLECULAR POLYHYDROXY COMPOUND (HAVING OH GROUP IN MONOMER UNIT) AND EPIHALOHYDRINS

AE01

AE02

AE03

AE05

AE07

. Polymers of phenols containing carbon-to-carbon double bonds

. . Polyvinyl phenols e.g. polyhydroxystyrenes

. . Polyisopropenyl phenols

. Phenol-aralkyl resins

. Other macromolecular polyhydroxy compounds

AF00
EPOXY RESIN OBTAINED FROM EPIHALOHYDRINS WITH PHENOL-ALDEHYDE CONDENSATE

AF01

AF03

AF05

AF06

AF07

AF08

AF09

AF10

. Phenolic resin glycidyl ether in general

. Phenolic components of condensates being specified e.g. trihydric or more phenols

. . Monohydric phenols including. naphthols

. . . Phenols including phenol novolak resins

. . . . Phenols having substituents

. . . . . Alkyl groups

. . . . . Carbon-to-carbon double bonds containing groups

. . . . . Halogen-containing groups

AF11

AF12

AF13

AF15

AF16

AF17

AF19

. . . . . Oxygen-containing groups other than phenolic OH groups

. . . . . . Carboxyl (COOH) containing groups

. . . . . Groups containing atoms other than carbon hydrogen oxygen or halogens

. . Dihydric phenols including dioxynaphthalenes

. . . Mononuclear dihydric phenols

. . . . having substituents

. . . Bisphenols

AF21

AF22

AF23

AF24

AF26

AF27

AF28

AF29

AF30

. . . . having substituents in the phenol nucleus

. . . . . Alkyl groups

. . . . . Halogen-containing groups

. . . . . Oxygen-containing groups other than phenolic OH groups

. . . . (X) being single bonds

. . . . (X) being hydrocarbon groups e.g. bisphenols A or F

. . . . . Halogen-containing groups

. . . . (X) being oxygen-containing groups

. . . . (X) being nitrogen-containing groups

AF31

AF33

AF34

AF35

AF36

AF37

. . . . (X) being atoms other than carbon hydrogen oxygen nitrogen sulfur phosphorus or halogens

. characterised by aldehyde components of condensates

. . Acetaldehydes

. . Aldehydes containing carbon-to-carbon double bonds e.g. crotonaldehydes

. . Aromatic aldehydes e.g. salicylaldehydes

. . . containing carbon-to-carbon double bonds e.g. cinnamaldehydes

AG00
EPOXY RESIN OBTAINED FROM CARBOXYLIC ACID AND EPIHALOHYDRINS, E.G. GLYCIDYL ESTER BASED EPOXY RESIN

AG01

AG03

AG04

AG05

AG06

AG07

AG08

AG09

AG10

. Monocarboxylic acids containing OH groups e.g. oxybenzoic acids

. Dicarboxylic acids

. . aliphatic

. . . containing carbon-to-carbon double bonds

. . alicyclic e.g. tetrahydrophthalic acid diglycidyl esters

. . aromatic e.g. phthalic acid diglycidyl esters

. . containing nitrogen

. . . Nitrogen-containing hetero rings

. . . . Imide rings

AG11

AG13

. . containing other atoms than carbon hydrogen oxygen nitrogen or halogens

. Trivalent or more carboxylic acids

AH00
EPOXY RESIN OBTAINED FROM AMINE AND EPIHALOHYDRINS, E.G. GLYCIDYL AMINE BASED EPOXY RESIN

AH01

AH02

AH04

AH05

AH06

AH07

AH08

AH09

AH10

. Monoamines

. . containing OH groups

. Diamines

. . aliphatic

. . alicyclic

. . aromatic

. . containing oxygen

. . . containing OH groups

. . . . having two amino groups in one phenol nucleus

AH11

AH12

AH13

AH15

AH16

AH17

AH18

AH19

AH20

. . . containing ether groups (-O-)

. . . Oxygen-containing hetero rings

. . containing other atoms than carbon hydrogen oxygen nitrogen or halogens

. Trivalent or more polyamines

. . aliphatic

. . alicyclic

. . aromatic

. . containing oxygen

. . containing other atoms than carbon hydrogen oxygen nitrogen or halogens

AJ00
OTHER POLYVALENT EPOXY COMPOUND, I.E. LOW MOLECULAR WEIGHT POLYVALENT EPOXY COMPOUND

AJ01

AJ02

AJ03

AJ05

AJ06

AJ07

AJ08

AJ09

AJ10

. having two epoxy groups in molecule

. having three epoxy groups in the molecule

. having four or more epoxy groups in the molecule

. Aliphatic polyvalent epoxy compounds

. . containing halogens

. . containing carbon-to-carbon double bonds

. Alicyclic polyvalent epoxy compounds e.g. alicyclic epoxy resins

. . having epoxy groups condensed in rings

. . . containing carbon-to-oxygen double bonds

AJ11

AJ12

AJ13

AJ14

AJ15

AJ16

AJ17

AJ18

AJ19

AJ20

. . having epoxy groups not being condensed in rings

. . . containing carbon-to-oxygen double bonds

. . . having substituents on rings

. Aromatic polyvalent epoxy compounds

. containing oxygen other than epoxy groups (AJ10 and AJ12 take precedence)

. . Oxygen-containing hetero rings

. containing nitrogen

. . Nitrogen-containing hetero rings

. containing sulfur

. containing phosphorus

AJ21

AJ22

AJ24

. containing silicon

. containing other atoms than carbon hydrogen oxygen nitrogen sulfur phosphorus silicon or halogens

. having one epoxy group and carbon-to-carbon double bonds in one molecule (Exceptions)

AK00
OTHER POLYVALENT EPOXY COMPOUND, I.E. MACROMOLECULAR POLYVALENT EPOXY COMPOUND

AK01

AK02

AK03

AK04

AK05

AK06

AK08

AK09

AK10

. Epoxidation of unsaturated polymers e.g. oxidation of bonds (Image 27)

. . Conjugated diene based polymers or copolymers

. . . Polybutadienes

. . Vinyl styrene polymers or copolymers e.g. divinylbenzenes

. . Allyl etherified novolaks

. . Other unsaturated polymers

. Polymers of epoxy group-containing (Image 27) compounds including copolymers or graft copolymers

. . Glycidyl ethers containing carbon-to-carbon double bonds

. . Glycidyl esters containing carbon-to-carbon double bonds

AK11

AK12

AK13

AK14

AK15

AK17

AK19

. . . Glycidyl acrylates or methacrylates

. . . . Comonomers containing sulfur

. . . . Comonomers containing phosphorous

. . . . Comonomers containing silicon

. . Glycidyl amines containing carbon-to-carbon double bonds

. Polyvalent epoxy compounds containing polysiloxane sequences

. Other macromolecular polyvalent epoxy compounds

BA00
MANUFACTURING METHOD OF EPOXY RESIN

BA01

BA02

BA03

BA04

BA05

BA06

BA07

BA08

BA09

. Manufacturing methods (Hardening methods see viewpoint HA)

. . Adjusting epoxy equivalents

. . Adjusting OH group equivalents

. Post-treatment methods of epoxy resins (Chemical modification see viewpoints CA-CD.)

. Refining methods of epoxy resins

. . Removing impurities

. . . Removing halogens e.g. hydrolytic chlorine

. . Removing water

. Other methods

CA00
MODIFICATION OF EPOXY RESIN BY LOW MOLECULAR WEIGHT OXYGEN-CONTAINING COMPOUND

CA01

CA02

CA03

CA04

CA06

CA07

CA08

CA09

CA10

. Alcohols

. . monohydric

. . dihydric

. . trihydric or more

. Phenols

. . monohydric

. . dihydric

. . trihydric or more

. . containing halogens

CA11

CA13

CA15

CA16

CA17

CA18

CA19

CA20

. . containing carbon-to-carbon double bonds

. Aldehydes or ketones

. Carboxylic acids

. . aliphatic

. . . saturated

. . . . monohydric

. . . . dihydric or more

. . . unsaturated

CA21

CA22

CA23

CA24

CA25

CA26

CA28

CA29

CA30

. . . . monohydric e.g. acrylic or methacrylic acids or vinyl ester resins

. . . . divalent or more

. . . . . Polymeric fatty acids

. . alicyclic

. . aromatic

. . . Oxybenzoic acids

. Oxygen-containing hetero rings

. . Lactones

. Other oxygen-containing compounds

CB00
MODIFICATION OF EPOXY RESIN BY LOW MOLECULAR WEIGHT NITROGEN-CONTAINING COMPOUND

CB01

CB03

CB04

CB05

CB07

CB08

CB09

CB10

. Ammonia

. Amines

. . Monoamines

. . Polyamines

. . containing halogens

. . containing carbon-to-carbon double bonds

. . containing oxygen

. . . containing OH groups

CB11

CB12

CB13

CB14

CB15

CB16

CB18

CB19

CB20

. . . . containing hydroxyphenyl groups

. . . containing ether groups (-O-)

. . . Oxygen-containing hetero rings

. . . . Spiroacetals

. . . containing carboxyl groups (COOH) e.g. amino acids

. . . containing ester groups (COOR)

. Acid amides

. Compounds containing carbon-to-nitrogen double bonds e.g. ketimines or keto-imines

. . Isocyanates

CB21

CB22

CB23

CB24

CB26

. Compounds containing carbon-to-nitrogen triple bonds e.g. cyano compounds

. Nitrogen-containing hetero rings

. . Imidazoles

. . Lactams

. Compounds containing other nitrogen

CC00
MODIFICATION OF EPOXY RESIN BY LOW MOLECULAR WEIGHT COMPOUND OTHER THAN VIEWPOINTS CA AND CB

CC01

CC02

CC03

CC04

CC05

. Sulfur-containing compounds

. Phosphorus-containing compounds

. Silicon-containing compounds

. Compounds containing metal atoms

. by other compounds

CD00
MODIFICATION OF EPOXY RESIN BY MACROMOLECULAR COMPOUND

CD01

CD02

CD03

CD04

CD06

CD07

CD08

CD09

CD10

. Polymers obtained from reactions involving only (Image 28) including modification by graft polymerisation

. . Olefins

. . Acrylics

. . Dienes e.g. acrylonitrile-butadiene copolymers

. Polymers obtained from reactions other than reactions involving only carbon-to-carbon double bonds

. . Phenolic resins

. . Amino resins

. . Polyurethanes

. . Epoxy resins e.g. reaction products of two kinds or more epoxy resin

CD11

CD12

CD13

CD14

CD15

CD16

CD18

. . Polyesters

. . Polyethers e.g. phenoxy resins

. . Polyamides e.g. polyamide amines

. . Polyamines polyimides or polyamide acids

. . Sulfur-containing polymers e.g. polythioethers or polysulfones

. . Silicon-containing polymers e.g. polysiloxanes

. . Polymers obtained from reactions involving carbon-to-carbon triple bonds e.g. polyacetylenes

CD21

CD22

CD23

CD24

. Natural macromolecules

. . Natural rubber

. . Fats

. . Bituminous materials e.g. asphalt

DA00
HARDENER OR HARDENING ACCELERATOR OF EPOXY RESIN

DA01

DA02

DA04

DA05

DA06

DA07

DA09

DA10

. Epoxy hardeners in general

. Epoxy hardening accelerators in general

. using in combination with hardeners or hardening accelerators

. . two kinds

. . three kinds

. . four or more kinds

. using reaction products of a plurality of hardeners or hardening accelerators

. Latent hardeners e.g. one-liquid types

DB00
ACTIVE HYDROGEN COMPOUNDS, E.G. OXYGEN-CONTAINING COMPOUNDS

DB01

DB02

DB03

DB05

DB06

DB07

DB08

DB09

DB10

. Alcohols

. . Polyhydric alcohols

. Metal alkoxides

. Phenols (Phenolic resins see FB08)

. . Phenol based hardeners in general (Phenolic resins see FB07)

. . containing halogens

. . containing carbon-to-carbon double bonds

. . containing ester groups (COOR)

. . having substituents on rings

DB11

DB12

DB14

DB15

DB16

DB17

DB18

DB19

DB20

. . Naphthols

. . Reaction products with epoxy resins

. Carboxylic acids

. . Polybasic acids or acid anhydride based hardeners in general

. . Monocarboxylic acids

. . Polycarboxylic acids

. . . aliphatic

. . . . containing halogens

. . . . containing carbon-to-carbon double bonds

DB21

DB22

DB23

DB24

DB25

DB27

DB28

DB29

DB30

. . . alicyclic e.g. tetrahydrophthalic acids hexahydrophthalic acids or hymic acids

. . . aromatic e.g. phthalic acids trimellitic acids. or pyromellitic acids

. . . containing ester groups (COOR)

. . . . Modified polyhydric alcohols

. . . Reaction products with epoxy resins

. Aldehydes

. Ketones

. Peroxides

. Other oxygen-containing compounds

DC00
ACTIVE HYDROGEN COMPOUND, E.G. NITROGEN-CONTAINING COMPOUND

DC01

DC02

DC03

DC04

DC05

DC06

DC07

DC08

DC09

DC10

. Amines (Ammonium salts see viewpoint GA) (Cyclic amines see DC38 or subdivisions)

. . Amine based hardeners in general

. . primary

. . secondary

. . tertiary

. . aliphatic

. . . containing halogens

. . . containing carbon-to-carbon double bonds

. . Alicyclic

. . aromatic

DC11

DC12

DC13

DC14

DC15

DC16

DC17

DC18

DC19

. . containing oxygen

. . . containing OH groups e.g. amino alcohols

. . . . containing hydroxyphenyl groups

. . . containing ether groups (-O-)

. . . containing carboxyl groups (COOH) e.g. amino acids

. . . containing ester groups (COOR)

. . . Oxygen-containing hetero rings

. . Reaction products with epoxy reins e.g. epoxy amine adducts

. . Boron trifluoride-amine complexes

DC21

DC22

DC23

DC25

DC26

DC27

DC28

DC30

. Acid amides

. . Amide amines (Polyamide amines see FB13)

. . containing hydroxyphenyl groups

. Urea compounds

. Compounds containing carbon-to-nitrogen double bonds e.g. guanidine biguanides

. . Isocyanates

. . Ketimines e.g. keto-imines

. Compounds containing carbon-to-nitrogen triple bonds e.g. diaminomaleonitriles

DC31

DC32

DC34

DC35

DC36

DC38

DC39

DC40

. . Dicyandiamides

. . Cyanic acid esters

. Compounds containing nitrogen-to-nitrogen bonds

. . Hydrazines or hydrazides

. . Amine imides

. Nitrogen-containing hetero rings

. . Saturated cyclic amines

. . Imidazole compounds

DC41

DC42

DC43

DC44

DC45

DC46

DC48

. . . Imidazole compounds in general

. . Compounds containing imide rings

. . . containing hydroxyphenyl groups

. . . containing amino groups

. . containing triazine rings e.g. cyanuric acids

. . Diazabicycloalkenes e.g. diazabicycloundecenes

. Other nitrogen-containing compounds

DD00
ACTIVE HYDROGEN COMPOUND, I.E. COMPOUND CONTAINING OTHER ATOMS THAN CARBON, HYDROGEN, OXYGEN, NITROGEN, OR HALOGEN

DD01

DD02

DD03

DD04

DD05

DD07

DD08

DD09

. Sulfur-containing compounds

. . Mercaptans or sulfides

. . containing sulfur-to-carbon double bonds e.g. thiocarboxylic acids or thioureas

. . containing sulfur-to-oxygen double bonds e.g. sulfonyl compounds

. . containing amino groups

. Phosphorus-containing compounds e.g. phosphines or phosphites

. Silicon-containing compounds (for substances containing OH groups or hydrolytic groups GA28 takes precedence)

. Other compounds

EA00
HARDENING OF EPOXY COMPOUND IN THE PRESENCE OF POLYMERIC GROUP (IMAGE 29) CONTAINING COMPOUND

EA01

EA02

EA03

EA04

EA05

EA06

EA07

EA09

EA10

. One carbon-to-carbon double bonds

. Two or more carbon-to-carbon double bonds

. Acrylic compounds e.g. acrylic or methacrylic acids or salts or acrylonitriles

. . Acrylates or methacrylates

. Diallylphthalates

. Maleimide compounds

. . Bismaleimides

. Macromolecular compounds containing carbon-to-carbon double bonds e.g. urethane acrylates or polyethylene glycol acrylates

. . Unsaturated polyesters

FA00
COMPOUNDING INGREDIENT OF EPOXY RESIN, E.G. LOW MOLECULAR WEIGHT COMPOUND

FA01

FA02

FA03

FA04

FA05

FA06

FA08

FA09

FA10

. Inorganic compounds e.g. inorganic fillers in general

. . Elements or metal compounds e.g. hydrides or carbides

. . Compounds containing halogens or oxygen

. . Compounds containing nitrogen sulfur or phosphorus

. . Silicon-containing compounds e.g. silica

. . Other inorganic compounds

. Organic compounds

. . Hydrocarbons or halogenated hydrocarbons

. . Oxygen-containing compounds

FA11

FA12

FA13

FA14

. . . Mono-epoxy compounds e.g. reactive diluents

. . Compounds containing nitrogen sulfur or phosphorus

. . Silicon-containing compounds (for substances containing OH groups or hydrolytic groups GA28 takes precedence)

. . Other compounds

FB00
COMPOUNDING INGREDIENT OF EPOXY RESIN, E.G. MACROMOLECULAR COMPOUND

FB01

FB02

FB03

FB04

FB05

FB06

FB07

FB08

FB09

FB10

. Polymers obtained from reactions involving only carbon-to-carbon double bonds

. . Olefins

. . Acrylics e.g. acrylates or methacrylates acrylamides or acrylonitrile polymers

. . Maleic acids

. . Dienes

. Polymers obtained by reactions other than reactions involving only carbon-to-carbon double bonds

. . Phenolic resins in general

. . . Specific phenolic resins i.e. having features

. . Amino resins

. . Polyurethanes

FB11

FB12

FB13

FB14

FB15

FB16

FB18

FB19

FB20

. . Polyesters

. . Polyethers e.g. phenoxy resins

. . Polyamides e.g. polyamide amines

. . Polyamines polyimides or polyamide acids

. . Sulfur-containing polymers e.g. polythioethers or polysulfones

. . Silicon-containing polymers e.g. polysiloxanes or silicone oil

. Natural macromolecules

. . Natural rubber

. . Fats

FB21

. . Bituminous materials e.g. asphalt

GA00
EPOXY RESIN HARDENING CATALYST

GA01

GA02

GA03

GA04

GA06

GA07

GA08

GA09

GA10

. Onium salts

. . Ammonium salts

. . Sulfonium salts

. . Phosphonium salts

. Boron-containing compounds (Boron trifluoride-amine complexes see DC19)

. Organometallic compounds

. . Aluminium compounds

. . Tin compounds

. . Titanium compounds

GA11

GA12

GA13

GA14

GA15

GA16

GA17

GA19

GA20

. . Carboxylic acid metal salts

. . . Octanoic acid salts

. . . Naphthenic acid salts

. . Dithiocarbamic acid salts

. . Metal chelate compounds

. . . Aluminium chelates

. . Metal acetylacetonates

. Lewis acids e.g. boron trifluoride (BF3) zinc chloride (ZnCl2) stannic chloride (SnCl4) iron chloride (FeCl3) or aluminium chloride (AlCl3)

. . Lewis acid salts

GA21

GA22

GA23

GA24

GA25

GA26

GA28

GA29

. . . Ammonium salts

. . . Sulfonium slats

. . . Phosphonium salts

. . . Iodonium salts

. . . Diazonium salts

. . . generating Lewis acids by irradiation of energy beams or light

. Compounds containing OH groups or hydrolytic groups bonded to silicon

. Other catalysts

HA00
HARDENING METHOD

HA01

HA02

HA03

HA05

HA06

HA07

HA08

HA09

. by energy beams

. . Photohardening

. . Electron beam hardening

. using treated hardeners

. . Surface treatment

. . Micro-encapsulation

. . Inclusion by cyclodextrins

. . Controlling diameters or shapes of particles

HA11

HA12

HA13

. Methods of mixing hardener compositions

. Controlling hardening temperature

. Methods having other features

JA00
USE

JA01

JA02

JA03

JA04

JA05

JA06

JA07

JA08

JA09

JA10

. Paint

. . for inner surfaces of cans or for retort

. . Powdery paint

. . Electrodeposition paint

. Varnishes e.g. insulating varnishes

. Adhesives

. Sealing agents e.g. semiconductor sealing agents

. Laminates e.g. multilayer wiring boards

. Resists e.g. photoresists

. . Solder resists

JA11

JA12

JA13

JA14

JA15

. Prepregs e.g. fibre-reinforced plastics (FRP)

. Tools

. Concrete repair

. Paving materials

. Other special applications e.g. toner or coagulants

KA00
FORM OF HARDENING COMPOSITION

KA01

KA02

KA03

KA04

KA05

KA06

KA07

. Solutions

. . Aqueous solutions

. Dispersions

. . Aqueous dispersions

. Powders

. Granular bodies

. having other features

4J036	EPOXY RESINS
	C08G59/00 -59/72