DE2117575A1 - Verfahren zur Herstellung von flammfesten Urethangruppen aufweisenden Schaumstoffen - Google Patents
Verfahren zur Herstellung von flammfesten Urethangruppen aufweisenden SchaumstoffenInfo
- Publication number
- DE2117575A1 DE2117575A1 DE19712117575 DE2117575A DE2117575A1 DE 2117575 A1 DE2117575 A1 DE 2117575A1 DE 19712117575 DE19712117575 DE 19712117575 DE 2117575 A DE2117575 A DE 2117575A DE 2117575 A1 DE2117575 A1 DE 2117575A1
- Authority
- DE
- Germany
- Prior art keywords
- groups
- weight
- polyisocyanates
- foams
- flame
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
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- 239000003063 flame retardant Substances 0.000 title description 9
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- 239000005056 polyisocyanate Substances 0.000 claims description 43
- 229920000570 polyether Polymers 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 29
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- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 16
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- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 claims description 7
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 claims description 5
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 claims description 5
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- 150000002513 isocyanates Chemical class 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 7
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- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 6
- -1 (hydroxyphenyl) - Chemical class 0.000 description 5
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- 230000002378 acidificating effect Effects 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
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- 238000010438 heat treatment Methods 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
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- 229920005862 polyol Polymers 0.000 description 3
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- 239000002244 precipitate Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,3-triazinane Chemical class C1CNNNC1 OYWRDHBGMCXGFY-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000004443 Ricinus communis Nutrition 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
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- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
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- 229910052698 phosphorus Inorganic materials 0.000 description 2
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- 238000002360 preparation method Methods 0.000 description 2
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- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
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- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 description 1
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- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
- GBMMWPJEWMJGCK-UHFFFAOYSA-N naphthalene-1,6,7-triol Chemical compound C1=CC(O)=C2C=C(O)C(O)=CC2=C1 GBMMWPJEWMJGCK-UHFFFAOYSA-N 0.000 description 1
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- VPRFQZSTJXHBHL-UHFFFAOYSA-N phenanthrene-9,10-diamine Chemical compound C1=CC=C2C(N)=C(N)C3=CC=CC=C3C2=C1 VPRFQZSTJXHBHL-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 238000010626 work up procedure Methods 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/7806—Nitrogen containing -N-C=0 groups
- C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
- C08G18/7831—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing biuret groups
-
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
- C08G18/727—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80 comprising distillation residues or non-distilled raw phosgenation products
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)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712117575 DE2117575A1 (de) | 1971-04-10 | 1971-04-10 | Verfahren zur Herstellung von flammfesten Urethangruppen aufweisenden Schaumstoffen |
| AU40237/72A AU468040B2 (en) | 1971-04-10 | 1972-03-21 | Process forthe production of flameproof foam plastics which contain urethane groups |
| AT301472A AT312941B (de) | 1971-04-10 | 1972-04-07 | Verfahren zur Herstellung von flammfesten, Urethangruppen aufweisenden Schaumstoffen |
| IT4944772A IT954410B (it) | 1971-04-10 | 1972-04-07 | Procedimento per produrre espansi ininfiammabili presentanti gruppi uretanici |
| NL7204703A NL7204703A (https=) | 1971-04-10 | 1972-04-07 | |
| BE781790A BE781790A (fr) | 1971-04-10 | 1972-04-07 | Procede de fabrication de matieres cellulaires ignifuges presentant desgroupes urethane |
| BR206472A BR7202064D0 (pt) | 1971-04-10 | 1972-04-07 | Processo para a fabricacao de substancias espumosas apresentando grupos uretano resistentes as chamas |
| ES401617A ES401617A1 (es) | 1971-04-10 | 1972-04-08 | Procedimiento para la obtencion de materiales espumados congrupos uretano, resistentes a la combustion. |
| ES401618A ES401618A1 (es) | 1971-04-10 | 1972-04-08 | Procedimiento para la obtencion de productos de poliadiciontermoplasticos. |
| GB1633772A GB1365629A (en) | 1971-04-10 | 1972-04-10 | Production of flameproof foam plastics which contain urethane groups |
| FR7212510A FR2132828B1 (https=) | 1971-04-10 | 1972-04-10 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712117575 DE2117575A1 (de) | 1971-04-10 | 1971-04-10 | Verfahren zur Herstellung von flammfesten Urethangruppen aufweisenden Schaumstoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2117575A1 true DE2117575A1 (de) | 1972-10-19 |
Family
ID=5804437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712117575 Pending DE2117575A1 (de) | 1971-04-10 | 1971-04-10 | Verfahren zur Herstellung von flammfesten Urethangruppen aufweisenden Schaumstoffen |
Country Status (10)
| Country | Link |
|---|---|
| AT (1) | AT312941B (https=) |
| AU (1) | AU468040B2 (https=) |
| BE (1) | BE781790A (https=) |
| BR (1) | BR7202064D0 (https=) |
| DE (1) | DE2117575A1 (https=) |
| ES (2) | ES401617A1 (https=) |
| FR (1) | FR2132828B1 (https=) |
| GB (1) | GB1365629A (https=) |
| IT (1) | IT954410B (https=) |
| NL (1) | NL7204703A (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116621263A (zh) * | 2022-08-19 | 2023-08-22 | 广东浪淘砂新型材料有限公司 | 一种搅拌站洗车废水用的消泡剂及其制备方法及其应用 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1484896A (fr) * | 1965-06-21 | 1967-06-16 | Allied Chem | Procédé de production de compositions stables à base de polyisocyanate |
-
1971
- 1971-04-10 DE DE19712117575 patent/DE2117575A1/de active Pending
-
1972
- 1972-03-21 AU AU40237/72A patent/AU468040B2/en not_active Expired
- 1972-04-07 BR BR206472A patent/BR7202064D0/pt unknown
- 1972-04-07 BE BE781790A patent/BE781790A/xx unknown
- 1972-04-07 NL NL7204703A patent/NL7204703A/xx unknown
- 1972-04-07 IT IT4944772A patent/IT954410B/it active
- 1972-04-07 AT AT301472A patent/AT312941B/de not_active IP Right Cessation
- 1972-04-08 ES ES401617A patent/ES401617A1/es not_active Expired
- 1972-04-08 ES ES401618A patent/ES401618A1/es not_active Expired
- 1972-04-10 GB GB1633772A patent/GB1365629A/en not_active Expired
- 1972-04-10 FR FR7212510A patent/FR2132828B1/fr not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116621263A (zh) * | 2022-08-19 | 2023-08-22 | 广东浪淘砂新型材料有限公司 | 一种搅拌站洗车废水用的消泡剂及其制备方法及其应用 |
| CN116621263B (zh) * | 2022-08-19 | 2024-01-05 | 广东浪淘砂新型材料有限公司 | 一种搅拌站洗车废水用的消泡剂及其制备方法及其应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU468040B2 (en) | 1973-09-27 |
| GB1365629A (en) | 1974-09-04 |
| BE781790A (fr) | 1972-10-09 |
| FR2132828A1 (https=) | 1972-11-24 |
| AT312941B (de) | 1974-01-25 |
| ES401618A1 (es) | 1975-02-16 |
| BR7202064D0 (pt) | 1973-05-31 |
| FR2132828B1 (https=) | 1978-06-09 |
| IT954410B (it) | 1973-08-30 |
| AU4023772A (en) | 1973-09-27 |
| ES401617A1 (es) | 1975-02-16 |
| NL7204703A (https=) | 1972-10-12 |
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