NO128138B - - Google Patents

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Info

Publication number: NO128138B
Authority: NO; Norway
Prior art keywords: reaction; catalyst; triethylenediamine; polyester; isocyanate
Prior art date: 1967-06-16

Application number

NO232668A

Other languages

English (en)

Norwegian (no)

Inventor

D Bridges

Original Assignee

Decca Ltd

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.)

1967-06-16

Filing date

1968-06-14

Publication date

1973-10-01

1968-06-14 Application filed by Decca Ltd filed Critical Decca Ltd

1973-10-01 Publication of NO128138B publication Critical patent/NO128138B/no

Links

IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical group C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims description 54
238000006243 chemical reaction Methods 0.000 claims description 53
239000003054 catalyst Substances 0.000 claims description 51
229920000728 polyester Polymers 0.000 claims description 27
239000012948 isocyanate Substances 0.000 claims description 21
-1 aryl isocyanate Chemical class 0.000 claims description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
150000002513 isocyanates Chemical class 0.000 claims description 15
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
229920002635 polyurethane Polymers 0.000 claims description 13
239000004814 polyurethane Substances 0.000 claims description 13
238000000034 method Methods 0.000 claims description 11
150000002440 hydroxy compounds Chemical class 0.000 claims description 10
229920005830 Polyurethane Foam Polymers 0.000 claims description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 7
238000004519 manufacturing process Methods 0.000 claims description 7
239000011496 polyurethane foam Substances 0.000 claims description 7
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
150000003673 urethanes Chemical class 0.000 claims description 4
230000008569 process Effects 0.000 claims description 3
150000005846 sugar alcohols Polymers 0.000 claims description 3
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical group CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000000047 product Substances 0.000 description 25
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
239000000126 substance Substances 0.000 description 11
125000005442 diisocyanate group Chemical group 0.000 description 10
239000006260 foam Substances 0.000 description 10
229920000642 polymer Polymers 0.000 description 10
150000001412 amines Chemical class 0.000 description 9
150000001875 compounds Chemical class 0.000 description 8
238000004132 cross linking Methods 0.000 description 8
239000011541 reaction mixture Substances 0.000 description 8
239000002253 acid Substances 0.000 description 7
230000015572 biosynthetic process Effects 0.000 description 7
239000003995 emulsifying agent Substances 0.000 description 6
239000000203 mixture Substances 0.000 description 6
HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 5
239000007795 chemical reaction product Substances 0.000 description 5
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 4
230000008901 benefit Effects 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
239000000787 lecithin Substances 0.000 description 4
229940067606 lecithin Drugs 0.000 description 4
235000010445 lecithin Nutrition 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
238000003756 stirring Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
YAIQCYZCSGLAAN-UHFFFAOYSA-N [Si+4].[O-2].[Al+3] Chemical compound [Si+4].[O-2].[Al+3] YAIQCYZCSGLAAN-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
230000003197 catalytic effect Effects 0.000 description 2
239000000539 dimer Substances 0.000 description 2
238000010494 dissociation reaction Methods 0.000 description 2
230000005593 dissociations Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
LBKPGNUOUPTQKA-UHFFFAOYSA-N ethyl n-phenylcarbamate Chemical compound CCOC(=O)NC1=CC=CC=C1 LBKPGNUOUPTQKA-UHFFFAOYSA-N 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
235000020778 linoleic acid Nutrition 0.000 description 2
239000000463 material Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 2
229920001228 polyisocyanate Polymers 0.000 description 2
239000005056 polyisocyanate Substances 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
150000003333 secondary alcohols Chemical class 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
125000005270 trialkylamine group Chemical group 0.000 description 2
XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
SKYZYDSNJIOXRL-BTQNPOSSSA-N (6ar)-6-methyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinoline-10,11-diol;hydrochloride Chemical compound Cl.C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 SKYZYDSNJIOXRL-BTQNPOSSSA-N 0.000 description 1
ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 description 1
QZWKEPYTBWZJJA-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine-4,4'-diisocyanate Chemical compound C1=C(N=C=O)C(OC)=CC(C=2C=C(OC)C(N=C=O)=CC=2)=C1 QZWKEPYTBWZJJA-UHFFFAOYSA-N 0.000 description 1
WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
235000001674 Agaricus brunnescens Nutrition 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
206010019233 Headaches Diseases 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
229920002347 Polypropylene succinate Polymers 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
230000001754 anti-pyretic effect Effects 0.000 description 1
239000002221 antipyretic Substances 0.000 description 1
229940067597 azelate Drugs 0.000 description 1
239000002585 base Substances 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
238000005266 casting Methods 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
230000001413 cellular effect Effects 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
HQPMKSGTIOYHJT-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2-diol Chemical compound OCCO.CC(O)CO HQPMKSGTIOYHJT-UHFFFAOYSA-N 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
231100000869 headache Toxicity 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
230000006698 induction Effects 0.000 description 1
238000009413 insulation Methods 0.000 description 1
239000010985 leather Substances 0.000 description 1
230000035800 maturation Effects 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
150000002780 morpholines Chemical class 0.000 description 1
VIJMMQUAJQEELS-UHFFFAOYSA-N n,n-bis(ethenyl)ethenamine Chemical compound C=CN(C=C)C=C VIJMMQUAJQEELS-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
235000019645 odor Nutrition 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000012071 phase Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
150000004885 piperazines Chemical class 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920003225 polyurethane elastomer Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
238000011417 postcuring Methods 0.000 description 1
238000003825 pressing Methods 0.000 description 1
VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
239000013014 purified material Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000007363 ring formation reaction Methods 0.000 description 1
238000010517 secondary reaction Methods 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003509 tertiary alcohols Chemical class 0.000 description 1
229920002725 thermoplastic elastomer Polymers 0.000 description 1
239000013638 trimer Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
239000012808 vapor phase Substances 0.000 description 1

Classifications

- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03H—IMPEDANCE NETWORKS, e.g. RESONANT CIRCUITS; RESONATORS
- H03H3/00—Apparatus or processes specially adapted for the manufacture of impedance networks, resonating circuits, resonators
- H03H3/007—Apparatus or processes specially adapted for the manufacture of impedance networks, resonating circuits, resonators for the manufacture of electromechanical resonators or networks
- H03H3/02—Apparatus or processes specially adapted for the manufacture of impedance networks, resonating circuits, resonators for the manufacture of electromechanical resonators or networks for the manufacture of piezoelectric or electrostrictive resonators or networks
- H03H3/04—Apparatus or processes specially adapted for the manufacture of impedance networks, resonating circuits, resonators for the manufacture of electromechanical resonators or networks for the manufacture of piezoelectric or electrostrictive resonators or networks for obtaining desired frequency or temperature coefficient
- G—PHYSICS
- G01—MEASURING; TESTING
- G01H—MEASUREMENT OF MECHANICAL VIBRATIONS OR ULTRASONIC, SONIC OR INFRASONIC WAVES
- G01H13/00—Measuring resonant frequency
- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03B—GENERATION OF OSCILLATIONS, DIRECTLY OR BY FREQUENCY-CHANGING, BY CIRCUITS EMPLOYING ACTIVE ELEMENTS WHICH OPERATE IN A NON-SWITCHING MANNER; GENERATION OF NOISE BY SUCH CIRCUITS
- H03B5/00—Generation of oscillations using amplifier with regenerative feedback from output to input
- H03B5/30—Generation of oscillations using amplifier with regenerative feedback from output to input with frequency-determining element being electromechanical resonator
- H03B5/32—Generation of oscillations using amplifier with regenerative feedback from output to input with frequency-determining element being electromechanical resonator being a piezoelectric resonator
- H03B5/36—Generation of oscillations using amplifier with regenerative feedback from output to input with frequency-determining element being electromechanical resonator being a piezoelectric resonator active element in amplifier being semiconductor device
- H03B5/366—Generation of oscillations using amplifier with regenerative feedback from output to input with frequency-determining element being electromechanical resonator being a piezoelectric resonator active element in amplifier being semiconductor device and comprising means for varying the frequency by a variable voltage or current
- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03L—AUTOMATIC CONTROL, STARTING, SYNCHRONISATION OR STABILISATION OF GENERATORS OF ELECTRONIC OSCILLATIONS OR PULSES
- H03L1/00—Stabilisation of generator output against variations of physical values, e.g. power supply
- H03L1/02—Stabilisation of generator output against variations of physical values, e.g. power supply against variations of temperature only
- H03L1/022—Stabilisation of generator output against variations of physical values, e.g. power supply against variations of temperature only by indirect stabilisation, i.e. by generating an electrical correction signal which is a function of the temperature
- H03L1/023—Stabilisation of generator output against variations of physical values, e.g. power supply against variations of temperature only by indirect stabilisation, i.e. by generating an electrical correction signal which is a function of the temperature by using voltage variable capacitance diodes
- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03L—AUTOMATIC CONTROL, STARTING, SYNCHRONISATION OR STABILISATION OF GENERATORS OF ELECTRONIC OSCILLATIONS OR PULSES
- H03L1/00—Stabilisation of generator output against variations of physical values, e.g. power supply
- H03L1/02—Stabilisation of generator output against variations of physical values, e.g. power supply against variations of temperature only
- H03L1/028—Stabilisation of generator output against variations of physical values, e.g. power supply against variations of temperature only of generators comprising piezoelectric resonators

Landscapes

Engineering & Computer Science (AREA)
Manufacturing & Machinery (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Oscillators With Electromechanical Resonators (AREA)
Piezo-Electric Or Mechanical Vibrators, Or Delay Or Filter Circuits (AREA)
Position Fixing By Use Of Radio Waves (AREA)
Polyurethanes Or Polyureas (AREA)

NO232668A 1967-06-16 1968-06-14 NO128138B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB2784467A GB1163064A (en)	1967-06-16	1967-06-16	Circuits for Controlling the Resonant Frequency of a Piezo-Electric Crystal or the like.

Publications (1)

Publication Number	Publication Date
NO128138B true NO128138B (de)	1973-10-01

Family

ID=10266224

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO232668A NO128138B (de)	1967-06-16	1968-06-14

Country Status (6)

Country	Link
JP (1)	JPS4842751B1 (de)
DK (1)	DK119618B (de)
FR (1)	FR1568658A (de)
GB (1)	GB1163064A (de)
NL (1)	NL150969B (de)
NO (1)	NO128138B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2233513A (en) *	1989-06-09	1991-01-09	Philips Electronic Associated	Oscillators

1967
- 1967-06-16 GB GB2784467A patent/GB1163064A/en not_active Expired
1968
- 1968-06-14 NO NO232668A patent/NO128138B/no unknown
- 1968-06-14 NL NL6808392A patent/NL150969B/xx unknown
- 1968-06-14 JP JP4061368A patent/JPS4842751B1/ja active Pending
- 1968-06-14 DK DK278768A patent/DK119618B/da unknown
- 1968-06-14 FR FR1568658D patent/FR1568658A/fr not_active Expired

Also Published As

Publication number	Publication date
DK119618B (da)	1971-02-01
NL150969B (nl)	1976-09-15
GB1163064A (en)	1969-09-04
NL6808392A (de)	1968-12-17
FR1568658A (de)	1969-05-23
JPS4842751B1 (de)	1973-12-14

Publication	Publication Date	Title
US2939851A (en)	1960-06-07	Preparation of urethanes wherein triethylene diamine is used as the catalyst
US4007140A (en)	1977-02-08	Tertiary amines as catalysts in polyurethane manufacture
US3124605A (en)	1964-03-10	Biuret polyisocyanates
US4031026A (en)	1977-06-21	Diphenylmethane diisocyanate compositions
US3336242A (en)	1967-08-15	Polyurethanes produced from ethylene oxide capped polyhydric alcohol-propylene oxide adducts
US5925781A (en)	1999-07-20	Prepolymers with low monomeric TDI content
US4450246A (en)	1984-05-22	Novel polyurethane catalysts in polyurethane foam process
NO822378L (no)	1983-01-10	Skum-fremstilling.
GB1537007A (en)	1978-12-29	Crosslinked polymers based on cyanic acid esters
DE69033885D1 (de)	2002-01-31	Isocyanatzusammensetzung und Verfahren für die Herstellung von Weichschaumstoffen daraus
GB889050A (en)	1962-02-07	Process for the manufacture of polyurethanes
KR960005794B1 (ko)	1996-05-01	폴리우레탄 발포체의 제조방법
US3544524A (en)	1970-12-01	Polyurethane polymers prepared from a chain extender and the transesterification product of 1,6-hexanediol with a diarylcarbonate
US3794621A (en)	1974-02-26	Polyurethane elastomers prepared from diamino-benzoic acid esters
US4709002A (en)	1987-11-24	Method for the preparation of rigid non-cellular reaction injection molded thermoset polyisocyanurate compositions
NO165076B (no)	1990-09-10	Termoplastisk, varmtsmeltende material og fremgangsmaate for fremstilling derav.
KR930008001A (ko)	1993-05-20	자유-유동성 폴리우레탄 분말 및 이의 제조방법
GB1034851A (en)	1966-07-06	Polyurethanes
US4071505A (en)	1978-01-31	Molecular weight control of polyurethane elastomers
US3037947A (en)	1962-06-05	Foamed polyurethane polymer and method of making same
JPH03152111A (ja)	1991-06-28	新規化学発泡剤
JPH0238583B2 (de)	1990-08-31
JP7330890B2 (ja)	2023-08-22	ポリウレタン製造用触媒
US3054757A (en)	1962-09-18	Polyurethane production with imines as catalysts
US3226368A (en)	1965-12-28	Process of preparing polyesterurethanes containing carbodiimide groups