SK51899A3 - Method for volume dyeing partially crystalline plastics and pigment compositions based on diaryldiketopyrrolo[3,4-c]pyrroles not inducing deformities - Google Patents

Method for volume dyeing partially crystalline plastics and pigment compositions based on diaryldiketopyrrolo[3,4-c]pyrroles not inducing deformities Download PDF

Info

Publication number: SK51899A3
Authority: SK; Slovakia
Prior art keywords: formula; group; pigment; hydrogen; halogen
Prior art date: 1998-04-22

Application number

SK518-99A

Other languages

English (en)

Slovak (sk)

Inventor

Franck R Flandrin

Guo-Hua Hu

Philippe Bugnon

Zhimin Hao

Original Assignee

Ciba Sc Holding Ag

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.)

1998-04-22

Filing date

1999-04-20

Publication date

2000-03-13

1999-04-20 Application filed by Ciba Sc Holding Ag filed Critical Ciba Sc Holding Ag

2000-03-13 Publication of SK51899A3 publication Critical patent/SK51899A3/sk

Links

239000000049 pigment Substances 0.000 title claims abstract description 75
239000000203 mixture Substances 0.000 title claims abstract description 28
238000000034 method Methods 0.000 title claims abstract description 27
229920001887 crystalline plastic Polymers 0.000 title claims abstract description 18
238000004043 dyeing Methods 0.000 title claims description 5
150000003233 pyrroles Chemical class 0.000 title description 5
230000001939 inductive effect Effects 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 29
125000000217 alkyl group Chemical group 0.000 claims abstract description 23
229910052736 halogen Inorganic materials 0.000 claims abstract description 14
239000003086 colorant Substances 0.000 claims abstract description 13
-1 cyano, carbamoyl Chemical group 0.000 claims abstract description 13
150000002367 halogens Chemical class 0.000 claims abstract description 13
125000005843 halogen group Chemical group 0.000 claims abstract description 11
239000000126 substance Substances 0.000 claims abstract description 8
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
230000008569 process Effects 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 28
239000001257 hydrogen Substances 0.000 claims description 26
239000000975 dye Substances 0.000 claims description 19
150000002431 hydrogen Chemical class 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 8
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 7
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 4
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 4
239000004952 Polyamide Substances 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
229920002647 polyamide Polymers 0.000 claims description 3
229920000728 polyester Polymers 0.000 claims description 3
229920001169 thermoplastic Polymers 0.000 claims description 3
239000004416 thermosoftening plastic Substances 0.000 claims description 3
229920001400 block copolymer Polymers 0.000 claims description 2
229920001519 homopolymer Polymers 0.000 claims description 2
229920000554 ionomer Polymers 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
229920005604 random copolymer Polymers 0.000 claims description 2
229920001897 terpolymer Polymers 0.000 claims description 2
238000001746 injection moulding Methods 0.000 abstract description 5
230000004075 alteration Effects 0.000 abstract 1
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
229920003023 plastic Polymers 0.000 description 9
239000004033 plastic Substances 0.000 description 9
239000000654 additive Substances 0.000 description 8
238000002347 injection Methods 0.000 description 8
239000007924 injection Substances 0.000 description 8
239000002245 particle Substances 0.000 description 7
239000011324 bead Substances 0.000 description 5
JNNHVXMCVRYTTN-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-3,6-dione Chemical compound C1=CC(Cl)=CC=C1C(NC1=O)=C2C1=C(C=1C=CC(Cl)=CC=1)NC2=O JNNHVXMCVRYTTN-UHFFFAOYSA-N 0.000 description 4
KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
125000003342 alkenyl group Chemical group 0.000 description 4
230000008859 change Effects 0.000 description 4
125000004433 nitrogen atom Chemical group N* 0.000 description 4
239000011368 organic material Substances 0.000 description 4
239000012860 organic pigment Substances 0.000 description 4
229920000098 polyolefin Polymers 0.000 description 4
NKHUXLDXYURVLX-UHFFFAOYSA-N 2h-pyrrolo[3,4-c]pyrrole-4,6-dione Chemical class N1C=C2C(=O)NC(=O)C2=C1 NKHUXLDXYURVLX-UHFFFAOYSA-N 0.000 description 3
239000004594 Masterbatch (MB) Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
238000004040 coloring Methods 0.000 description 3
238000002425 crystallisation Methods 0.000 description 3
230000008025 crystallization Effects 0.000 description 3
229920001903 high density polyethylene Polymers 0.000 description 3
239000004700 high-density polyethylene Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000003973 paint Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
230000029936 alkylation Effects 0.000 description 2
238000005804 alkylation reaction Methods 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
239000000976 ink Substances 0.000 description 2
229920000092 linear low density polyethylene Polymers 0.000 description 2
239000004707 linear low-density polyethylene Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
239000012744 reinforcing agent Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
125000000923 (C1-C30) alkyl group Chemical group 0.000 description 1
GSKQJYLCJVSPFR-UHFFFAOYSA-N 1,3-diphenyl-2h-pyrrolo[3,4-c]pyrrole-4,6-dione Chemical class C=12C(=O)NC(=O)C2=C(C=2C=CC=CC=2)NC=1C1=CC=CC=C1 GSKQJYLCJVSPFR-UHFFFAOYSA-N 0.000 description 1
AVNIQJJNAPFAFV-UHFFFAOYSA-N 6-(4-chlorophenyl)pyrrolo[3,4-c]pyrrole Chemical compound C1=CC(Cl)=CC=C1C1=NC=C2C1=CN=C2 AVNIQJJNAPFAFV-UHFFFAOYSA-N 0.000 description 1
JMBADVIVSPCVHP-UHFFFAOYSA-N 6-(4-tert-butylphenyl)pyrrolo[3,4-c]pyrrole Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NC=C2C1=CN=C2 JMBADVIVSPCVHP-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
229920002302 Nylon 6,6 Polymers 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001408 amides Chemical group 0.000 description 1
229920001871 amorphous plastic Polymers 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000008901 benefit Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
230000021615 conjugation Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000010408 film Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000013020 final formulation Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000002463 lignoceryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920001684 low density polyethylene Polymers 0.000 description 1
239000004702 low-density polyethylene Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
125000001802 myricyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
238000010534 nucleophilic substitution reaction Methods 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000019612 pigmentation Effects 0.000 description 1
230000000485 pigmenting effect Effects 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000001749 primary amide group Chemical group 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000003156 secondary amide group Chemical group 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/004—Diketopyrrolopyrrole dyes
- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0034—Mixtures of two or more pigments or dyes of the same type
- C09B67/0039—Mixtures of diketopyrrolopyrroles

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Coloring (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)

SK518-99A 1998-04-22 1999-04-20 Method for volume dyeing partially crystalline plastics and pigment compositions based on diaryldiketopyrrolo[3,4-c]pyrroles not inducing deformities SK51899A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH91598		1998-04-22
CH38099		1999-03-02

Publications (1)

Publication Number	Publication Date
SK51899A3 true SK51899A3 (en)	2000-03-13

Family

ID=25684402

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK518-99A SK51899A3 (en)	1998-04-22	1999-04-20	Method for volume dyeing partially crystalline plastics and pigment compositions based on diaryldiketopyrrolo[3,4-c]pyrroles not inducing deformities

Country Status (13)

Country	Link
US (3)	US6409956B1 (fr)
EP (1)	EP0952183B1 (fr)
JP (1)	JP4489867B2 (fr)
KR (1)	KR100607835B1 (fr)
CN (1)	CN1172979C (fr)
AT (1)	ATE289618T1 (fr)
AU (1)	AU766047B2 (fr)
CA (1)	CA2269587A1 (fr)
CZ (1)	CZ295621B6 (fr)
DE (1)	DE59911647D1 (fr)
ES (1)	ES2236981T3 (fr)
SK (1)	SK51899A3 (fr)
TW (1)	TW499464B (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP4019414B2 (ja)	2002-05-09	2007-12-12	ソニー株式会社	樹脂組成物及びその製造方法、並びにその成形品
BR0311950A (pt) *	2002-06-19	2005-03-29	Ciba Sc Holding Ag	Composições de pigmento que não produzem empenamento contendo pigmentos ftalocianinas
EP1523528B1 (fr) *	2002-07-22	2012-02-22	Basf Se	Dicetopyrrolopyrroles polymerisables, utilisation de ces composes dans des filtres couleurs et polymeres prepares a base de ces composes
DE10235573A1 (de) *	2002-08-03	2004-02-12	Clariant Gmbh	Pigmentzubereitungen auf Basis von Diketopyrrolopyrrolpigmenten zum verzugsfreien Pigmentieren von teilkristallinen Kunststoffen
EP1591487A4 (fr) *	2003-02-04	2006-04-05	Sony Corp	Composition de resine et procede de production d' un moulage en resine
US7417154B2 (en) *	2003-10-23	2008-08-26	Ciba Specialty Chemicals Corporation	Heat-stable diketopyrrolopyrrole pigment mixtures
DE102004039954A1 (de) *	2004-08-18	2006-02-23	Clariant Gmbh	Verfahren zum verzugsfreien Pigmentieren von teilkristallinen Kunststoffen
CN104892979B (zh) *	2014-12-31	2019-01-15	先尼科化工（上海）有限公司	在塑料中具有抗翘曲性能的颜料组合物
CN110791118A (zh) *	2018-08-01	2020-02-14	浙江浩川科技有限公司	吡咯并吡咯二酮类颜料衍生物合成方法及其制成产品用途

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3978036A (en) *	1972-11-28	1976-08-31	Pms Consolidated	Method of coloring and molding a shaped thermoplastic resin article
JPS5650741B2 (fr)	1974-11-20	1981-12-01
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1999
- 1999-04-14 ES ES99106256T patent/ES2236981T3/es not_active Expired - Lifetime
- 1999-04-14 AT AT99106256T patent/ATE289618T1/de not_active IP Right Cessation
- 1999-04-14 DE DE59911647T patent/DE59911647D1/de not_active Expired - Lifetime
- 1999-04-14 EP EP99106256A patent/EP0952183B1/fr not_active Expired - Lifetime
- 1999-04-20 SK SK518-99A patent/SK51899A3/sk unknown
- 1999-04-20 JP JP11212199A patent/JP4489867B2/ja not_active Expired - Lifetime
- 1999-04-20 US US09/294,484 patent/US6409956B1/en not_active Expired - Lifetime
- 1999-04-20 CA CA002269587A patent/CA2269587A1/fr not_active Abandoned
- 1999-04-20 CZ CZ19991405A patent/CZ295621B6/cs not_active IP Right Cessation
- 1999-04-21 TW TW088106381A patent/TW499464B/zh not_active IP Right Cessation
- 1999-04-21 KR KR1019990014194A patent/KR100607835B1/ko not_active Expired - Lifetime
- 1999-04-21 CN CNB991052196A patent/CN1172979C/zh not_active Expired - Lifetime
- 1999-04-22 AU AU23936/99A patent/AU766047B2/en not_active Ceased
2002
- 2002-03-18 US US10/100,602 patent/US6790884B2/en not_active Expired - Lifetime
2003
- 2003-10-29 US US10/696,012 patent/US6890977B2/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
ES2236981T3 (es)	2005-07-16
US20040092627A1 (en)	2004-05-13
CZ295621B6 (cs)	2005-09-14
DE59911647D1 (de)	2005-03-31
KR100607835B1 (ko)	2006-08-04
CN1172979C (zh)	2004-10-27
US6890977B2 (en)	2005-05-10
KR19990083373A (ko)	1999-11-25
TW499464B (en)	2002-08-21
EP0952183B1 (fr)	2005-02-23
JP4489867B2 (ja)	2010-06-23
US6790884B2 (en)	2004-09-14
CZ140599A3 (cs)	1999-11-17
CA2269587A1 (fr)	1999-10-22
JPH11349844A (ja)	1999-12-21
CN1236784A (zh)	1999-12-01
ATE289618T1 (de)	2005-03-15
AU2393699A (en)	1999-11-04
AU766047B2 (en)	2003-10-09
US20020178516A1 (en)	2002-12-05
EP0952183A1 (fr)	1999-10-27
US6409956B1 (en)	2002-06-25

Publication	Publication Date	Title
US20080194742A1 (en)	2008-08-14	Method for Undistorted Pigmentation of Partially Crystalline Plastics
AU700599B2 (en)	1999-01-07	Colorant preparation for producing masterbatches
US6790884B2 (en)	2004-09-14	Warp-free pigment compositions comprising diaryldiketopyrrolo[3,4-c]pyrroles
CA2199094A1 (fr)	1997-09-06	Solutions solides ternaires de dicetopyrrolopyrroles et de quinacridones - 1,4
JPH0718198A (ja)	1995-01-20	２、９−ジクロロキナクリドン顔料をベースとした組成物
JP4832437B2 (ja)	2011-12-07	部分結晶性プラスチックの歪みのない着色のための方法
EP1486537B1 (fr)	2007-09-05	Compositions pigmentaires et leur utilisation dans des matières plastiques.
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EP1513899B1 (fr)	2006-11-29	Compositions pigmentaires exemptes de deformations, comprenant des pigments de phtalocyanine
US5527922A (en)	1996-06-18	Pyrrolo[3,4-c]pyrroles containing cyanimino groups
GB2279078A (en)	1994-12-21	Dyes in salt form
JP4374837B2 (ja)	2009-12-02	プラスチック用着色剤およびその使用
JP2004083672A (ja)	2004-03-18	プラスチック用着色剤およびその使用
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