CH392878A - Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen - Google Patents

Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen

Info

Publication number: CH392878A
Authority: CH; Switzerland
Prior art keywords: weight; parts; siloxane; block polymer; mixed
Prior art date: 1958-09-04

Application number

CH7751559A

Other languages

German (de)

English (en)

Inventor

Henry Saunders James

George Gemeinhardt Paul

Original Assignee

Mobay Chemical Corp

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.)

1958-09-04

Filing date

1959-08-28

Publication date

1965-05-31

1959-08-28 Application filed by Mobay Chemical Corp filed Critical Mobay Chemical Corp

1965-05-31 Publication of CH392878A publication Critical patent/CH392878A/de

Links

239000006260 foam Substances 0.000 title claims description 29
238000000034 method Methods 0.000 title claims description 15
238000004519 manufacturing process Methods 0.000 title claims description 6
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 title claims description 5
229920000642 polymer Polymers 0.000 claims description 27
229920000570 polyether Polymers 0.000 claims description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
238000006243 chemical reaction Methods 0.000 claims description 10
229920001228 polyisocyanate Polymers 0.000 claims description 6
239000005056 polyisocyanate Substances 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 4
238000005187 foaming Methods 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003368 amide group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
125000005702 oxyalkylene group Chemical group 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims 1
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 21
239000004721 Polyphenylene oxide Substances 0.000 description 14
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 13
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 11
229920001451 polypropylene glycol Polymers 0.000 description 10
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 10
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
239000000203 mixture Substances 0.000 description 9
JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 8
125000005442 diisocyanate group Chemical group 0.000 description 7
-1 B. OH Chemical group 0.000 description 6
235000011187 glycerol Nutrition 0.000 description 6
HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 5
239000012948 isocyanate Substances 0.000 description 5
150000002513 isocyanates Chemical class 0.000 description 5
229920002545 silicone oil Polymers 0.000 description 5
150000001875 compounds Chemical class 0.000 description 4
238000009833 condensation Methods 0.000 description 4
230000005494 condensation Effects 0.000 description 4
125000000524 functional group Chemical group 0.000 description 4
239000000047 product Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
125000006353 oxyethylene group Chemical group 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
AXFVIWBTKYFOCY-UHFFFAOYSA-N 1-n,1-n,3-n,3-n-tetramethylbutane-1,3-diamine Chemical compound CN(C)C(C)CCN(C)C AXFVIWBTKYFOCY-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
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 2
TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical class O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
VFDYEMVVNIPATA-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;propane-1,2,3-triol Chemical compound OCC(O)CO.CCC(CO)(CO)CO VFDYEMVVNIPATA-UHFFFAOYSA-N 0.000 description 1
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
125000005263 alkylenediamine group Chemical group 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
150000005840 aryl radicals Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
230000001788 irregular Effects 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
238000011031 large-scale manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229940068917 polyethylene glycols Drugs 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/08—Polyurethanes from polyethers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2483/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyurethanes Or Polyureas (AREA)

CH7751559A 1958-09-04 1959-08-28 Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen CH392878A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US75889058A	1958-09-04	1958-09-04

Publications (1)

Publication Number	Publication Date
CH392878A true CH392878A (de)	1965-05-31

Family

ID=25053508

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH7751559A CH392878A (de)	1958-09-04	1959-08-28	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen

Country Status (3)

Country	Link
CH (1)	CH392878A (da)
DK (1)	DK110075C (da)
GB (1)	GB923403A (da)

1959
- 1959-08-28 CH CH7751559A patent/CH392878A/de unknown
- 1959-09-03 DK DK313559A patent/DK110075C/da active
- 1959-09-04 GB GB3029159A patent/GB923403A/en not_active Expired

Also Published As

Publication number	Publication date
DK110075C (da)	1968-09-16
GB923403A (en)	1963-04-10

Publication	Publication Date	Title
DE69624206T2 (de)	2003-04-17	Ein Verfahren zur Herstellung von weichen Polyurethanschäumen
DE1170628B (de)	1964-05-21	Verfahren zur Herstellung von, gegebenenfalls verschaeumten, Polyurethanen
DE2034171A1 (de)	1971-01-14	Verfahren zur Herstellung von ge schäumten Polyurethanen
DE1544634A1 (de)	1969-07-17	Verfahren zur Herstellung von flexiblem Polyurethanschaum
DE2129988A1 (de)	1972-02-03	Polyurethanschaeume
DE3928867C1 (da)	1990-10-11
DE69127500T2 (de)	1998-01-08	Allein mit Wasser verschäumte Polyurethanschaumstoffe
DE69213498T2 (de)	1997-02-06	Zellöffnende Verbindungen für Polyurethanschaumstoff Tenside
DE2711735A1 (de)	1977-09-22	Verfahren zur herstellung von weichen und superweichen polyurethanschaeumen
DE1213988B (de)	1966-04-07	Verfahren zur gegebenenfalls einstufigen Herstellung von Polyurethanschaumstoffen
DE1122698B (de)	1962-01-25	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE69010982T2 (de)	1994-11-17	Polyurethan-Weichschaumstoffe sowie Verfahren zu deren Herstellung.
DE1078322B (de)	1960-03-24	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE1282949B (de)	1968-11-14	Verfahren zur Herstellung biegsamer Polyesterurethanschaumstoffe
DE2509478A1 (de)	1975-09-11	Verfahren zur herstellung von polyaetherurethanschaeumen mit hoher rueckprallelastizitaet
DE1215921B (de)	1966-05-05	Verfahren zur einstufigen Herstellung von flexiblen Polyurethanschaumstoffen
DE3215317C1 (de)	1983-06-09	Verfahren zur Herstellung hochelastischer kalthaertender Polyurethanschaumstoffe
AT244061B (de)	1965-12-10	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE1769187A1 (de)	1971-10-21	Weicher und hydrophiler Polyurethanschaumstoff und Verfahren zu seiner Herstellung
CH392878A (de)	1965-05-31	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE1226297B (de)	1966-10-06	Verwendung von Siloxan-Oxyalkylen-Blockmischpolymeren als Schaumstabilisatoren bei der Herstellung von Polyurethanschaumstoffen
DE2162371C2 (de)	1982-12-16	Organopolysiloxan-Block-Copolymere, Verfahren und Zwischenprodukte zu deren Herstellung und Verwendung der Blockcopolymeren
AT243520B (de)	1965-11-10	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE1104690B (de)	1961-04-13	Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen
DE1291613B (de)	1969-03-27	Biegsame Polyurethanschaumverbindung fuer Polsterungen