CH615202A5 - Process for preparing coloured polyurethane foams - Google Patents

Process for preparing coloured polyurethane foams Download PDF

Info

Publication number: CH615202A5
Authority: CH; Switzerland
Prior art keywords: polyurethane foams; foam; water; dye; groups
Prior art date: 1973-11-20

Application number

CH1532474A

Other languages

German (de)

English (en)

Inventor

Konrad Nonn

Reinhold Hoernle

Juergen Koerner

Michael Kressner

Karlheinz Wolf

Original Assignee

Bayer 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.)

1973-11-20

Filing date

1974-11-18

Publication date

1980-01-15

1974-11-18 Application filed by Bayer Ag filed Critical Bayer Ag

1980-01-15 Publication of CH615202A5 publication Critical patent/CH615202A5/de

Links

229920005830 Polyurethane Foam Polymers 0.000 title description 9
239000011496 polyurethane foam Substances 0.000 title description 9
238000004519 manufacturing process Methods 0.000 title description 3
239000000975 dye Substances 0.000 description 15
239000006260 foam Substances 0.000 description 14
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000002904 solvent Substances 0.000 description 10
238000009835 boiling Methods 0.000 description 9
239000011148 porous material Substances 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
235000011037 adipic acid Nutrition 0.000 description 6
239000001361 adipic acid Substances 0.000 description 6
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
150000001298 alcohols Chemical class 0.000 description 5
238000000034 method Methods 0.000 description 5
239000000049 pigment Substances 0.000 description 5
229920000728 polyester Polymers 0.000 description 5
229920000570 polyether Polymers 0.000 description 5
239000004721 Polyphenylene oxide Substances 0.000 description 4
-1 amino, hydroxyl Chemical group 0.000 description 4
239000000203 mixture Substances 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000012190 activator Substances 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
125000003710 aryl alkyl group Chemical group 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
229960002380 dibutyl phthalate Drugs 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
239000012948 isocyanate Substances 0.000 description 3
150000002596 lactones Chemical class 0.000 description 3
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000005907 alkyl ester group Chemical group 0.000 description 2
239000000987 azo dye Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000010924 continuous production Methods 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
238000005187 foaming Methods 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229910052757 nitrogen Chemical group 0.000 description 2
229920001228 polyisocyanate Polymers 0.000 description 2
239000005056 polyisocyanate Substances 0.000 description 2
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
239000000126 substance Substances 0.000 description 2
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
NCKPQOUTAMSEAO-UHFFFAOYSA-N 4-[(4-aminophenyl)diazenyl]phenol Chemical compound Nc1ccc(cc1)N=Nc1ccc(O)cc1 NCKPQOUTAMSEAO-UHFFFAOYSA-N 0.000 description 1
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical class C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
125000006487 butyl benzyl group Chemical group 0.000 description 1
229930188620 butyrolactone Natural products 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
230000001788 irregular Effects 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
IRIAEXORFWYRCZ-UHFFFAOYSA-N n-butyl benzyl phthalate Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Chemical group 0.000 description 1
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
125000005628 tolylene group Chemical group 0.000 description 1
125000006000 trichloroethyl group Chemical group 0.000 description 1
229960001147 triclofos Drugs 0.000 description 1
229940113165 trimethylolpropane Drugs 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- 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
- C08G18/30—Low-molecular-weight compounds

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyurethanes Or Polyureas (AREA)
Coloring (AREA)

CH1532474A 1973-11-20 1974-11-18 Process for preparing coloured polyurethane foams CH615202A5 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19732357933 DE2357933A1 (de)	1973-11-20	1973-11-20	Verfahren zur herstellung gefaerbter polyurethan-schaumstoffe

Publications (1)

Publication Number	Publication Date
CH615202A5 true CH615202A5 (en)	1980-01-15

Family

ID=5898624

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1532474A CH615202A5 (en)	1973-11-20	1974-11-18	Process for preparing coloured polyurethane foams

Country Status (10)

Country	Link
JP (1)	JPS5084696A (it)
BE (1)	BE822279A (it)
BR (1)	BR7409683A (it)
CH (1)	CH615202A5 (it)
DE (1)	DE2357933A1 (it)
ES (1)	ES432072A1 (it)
FR (1)	FR2251586B1 (it)
GB (1)	GB1472905A (it)
IT (1)	IT1025801B (it)
NL (1)	NL7415065A (it)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5354299A (en) *	1976-10-26	1978-05-17	Nippon Soda Co Ltd	Foamed product
DE19620989A1 (de) *	1996-05-24	1997-11-27	Bayer Ag	Pigmentpräparationen
RU2208019C2 (ru) *	2001-08-29	2003-07-10	Федеральное государственное унитарное предприятие "Научно-исследовательский институт полимерных материалов"	Способ получения литьевого полиуретанового эластомера
DE102007046751A1 (de)	2007-09-28	2009-04-02	Dystar Textilfarben Gmbh & Co. Deutschland Kg	Farbstoffe für die Polymerfärbung, Verfahren zu deren Herstellung und deren Verwendung
DE102008039951A1 (de)	2008-08-27	2010-03-04	Dystar Textilfarben Gmbh & Co. Deutschland Kg	Farbstoffe für die Polymerfärbung, Verfahren zu deren Herstellung und deren Verwendung
DE102008054792A1 (de)	2008-12-17	2010-06-24	Dystar Textilfarben Gmbh & Co. Deutschland Kg	Farbstoffe für die Polymerfärbung, Verfahren zu deren Herstellung und deren Verwendung

1973
- 1973-11-20 DE DE19732357933 patent/DE2357933A1/de not_active Withdrawn
1974
- 1974-11-18 CH CH1532474A patent/CH615202A5/de not_active IP Right Cessation
- 1974-11-18 IT IT2956374A patent/IT1025801B/it active
- 1974-11-18 JP JP49132127A patent/JPS5084696A/ja active Pending
- 1974-11-18 BE BE150579A patent/BE822279A/xx unknown
- 1974-11-19 NL NL7415065A patent/NL7415065A/xx not_active Application Discontinuation
- 1974-11-19 ES ES432072A patent/ES432072A1/es not_active Expired
- 1974-11-19 BR BR968374A patent/BR7409683A/pt unknown
- 1974-11-19 GB GB5002674A patent/GB1472905A/en not_active Expired
- 1974-11-20 FR FR7438141A patent/FR2251586B1/fr not_active Expired

Also Published As

Publication number	Publication date
JPS5084696A (it)	1975-07-08
IT1025801B (it)	1978-08-30
BE822279A (fr)	1975-05-20
DE2357933A1 (de)	1975-05-22
NL7415065A (nl)	1975-05-22
ES432072A1 (es)	1976-11-01
GB1472905A (en)	1977-05-11
FR2251586A1 (it)	1975-06-13
FR2251586B1 (it)	1978-06-16
BR7409683A (pt)	1976-05-25

Legal Events

Date	Code	Title	Description
1982-07-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2259435C3 (de)	1975-06-19	Verfahren zur Herstellung gefärbter Polyurethanschaumstoffe
DE2557619C3 (de)	1978-03-23	Stabilisierte Polyätherpolyole
DE2120921A1 (de)	1972-06-15	Verfahren zur Herstellung von eine ohge Flüssigkeit enthaltenden Mikro kapseln
DE2530809A1 (de)	1977-02-03	Verfahren zur faerbung von polyurethankunststoffen
DE2723657C3 (de)	1979-07-19	Zubereitung mit hohem Feststoff gehalt
EP0735109A2 (de)	1996-10-02	Wässrige Pigmentpräparationen
DE1812997A1 (de)	1969-07-10	Modifizierte Polyester
DE60105021T2 (de)	2005-08-11	Farbstarke polymerische farbstoffe mit einer niedrigen viskosität
DE2451646A1 (de)	1975-05-07	Haertbare harzmassen
CH615202A5 (en)	1980-01-15	Process for preparing coloured polyurethane foams
DE1028773B (de)	1958-04-24	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE19737184A1 (de)	1999-03-04	Verfahren zur Verringerung des Amingehalts von Recyclatpolyolen
DE3209676A1 (de)	1982-11-18	Katalysator-system und verfahren zur herstellung von polyurethan
DE1669611A1 (de)	1971-03-18	Zellulare Polyurethane und Verfahren zu ihrer Herstellung
DE3803810A1 (de)	1989-08-17	Pigment- und russpraeparationen
DE2444432A1 (de)	1975-03-20	Verfahren zur waermestabilisierung von polyurethanen
EP0065283A1 (de)	1982-11-24	Verdickungsmischungen, Verfahren zur Herstellung von Transferdruckpapieren unter Verwendung dieser Mischungen und die so erhaltenen Papiere
EP0764701A2 (de)	1997-03-26	Pigmentpräparationen
DE2100412B2 (de)	1975-05-22	Nitrocellulosegranulat und Verfahren zu seiner Herstellung
DE3115651C2 (it)	1992-04-23
DE1900759B2 (de)	1976-12-02	Verfahren zur kontinuierlichen herstellung von gefaerbten polyurethan- schaumstoffen
DE1028771B (de)	1958-04-24	Verfahren zur kontinuierlichen Herstellung gefaerbter Polyurethan-Schaumstoffe
DE2402839B2 (de)	1978-06-22	Pigmentpräparationen
DE1900759C3 (de)	1977-07-28	Verfahren zur kontinuierlichen Herstellung von gefärbten Polyurethan-Schaumstoffen
DE2933777A1 (de)	1980-02-28	Verfahren zur verhinderung der farbwanderung in formteilen aus polyoxymethylenharzen