KR970021120A - 정형외과용 경질 폴리우레탄 폼 및 이의 제조방법 - Google Patents
정형외과용 경질 폴리우레탄 폼 및 이의 제조방법 Download PDFInfo
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- KR970021120A KR970021120A KR1019960047929A KR19960047929A KR970021120A KR 970021120 A KR970021120 A KR 970021120A KR 1019960047929 A KR1019960047929 A KR 1019960047929A KR 19960047929 A KR19960047929 A KR 19960047929A KR 970021120 A KR970021120 A KR 970021120A
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- Prior art keywords
- polyol
- polyurethane foam
- orthopedic
- parts
- rigid polyurethane
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- 229920005830 Polyurethane Foam Polymers 0.000 title claims abstract 12
- 239000011496 polyurethane foam Substances 0.000 title claims abstract 12
- 230000000399 orthopedic effect Effects 0.000 title claims abstract 9
- 238000004519 manufacturing process Methods 0.000 title claims abstract 6
- 238000001356 surgical procedure Methods 0.000 title 1
- 229920005862 polyol Polymers 0.000 claims abstract 16
- 150000003077 polyols Chemical class 0.000 claims abstract 16
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 claims abstract 6
- 239000004604 Blowing Agent Substances 0.000 claims abstract 5
- 150000001412 amines Chemical class 0.000 claims abstract 5
- 239000003054 catalyst Substances 0.000 claims abstract 5
- 239000000945 filler Substances 0.000 claims abstract 4
- 238000000034 method Methods 0.000 claims abstract 4
- 239000000796 flavoring agent Substances 0.000 claims abstract 2
- 235000013355 food flavoring agent Nutrition 0.000 claims abstract 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical group C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims 4
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 2
- 239000003242 anti bacterial agent Substances 0.000 claims 2
- 229960002887 deanol Drugs 0.000 claims 2
- 239000012972 dimethylethanolamine Substances 0.000 claims 2
- 229910004298 SiO 2 Inorganic materials 0.000 claims 1
- 229910010413 TiO 2 Inorganic materials 0.000 claims 1
- 239000003205 fragrance Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 230000000845 anti-microbial effect Effects 0.000 abstract 1
- 239000004599 antimicrobial Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
- 238000002834 transmittance Methods 0.000 abstract 1
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- C—CHEMISTRY; METALLURGY
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- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
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- 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
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
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- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/32—Esters thereof
- C07F9/3205—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3211—Esters of acyclic saturated acids which can have further substituents on alkyl
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- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/42—Halides thereof
- C07F9/425—Acid or estermonohalides thereof, e.g. RP(=X)(YR)(Hal) (X, Y = O, S; R = H, or hydrocarbon group)
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
- C07F9/4403—Amides thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4407—Amides of acyclic saturated acids which can have further substituents on alkyl
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/53—Organo-phosphine oxides; Organo-phosphine thioxides
- C07F9/5304—Acyclic saturated phosphine oxides or thioxides
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/60—Quinoline or hydrogenated quinoline ring systems
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/65031—Five-membered rings having the nitrogen atoms in the positions 1 and 2
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6518—Five-membered rings
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/653—Five-membered rings
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6536—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and sulfur atoms with or without oxygen atoms, as the only ring hetero atoms
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
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- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
- C07F9/657181—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative
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- 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
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
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Abstract
Description
Claims (7)
- (가) 메틸렌디이소시아네이트 또는 변성-메틸렌디이소시아네이트에 3∼8의 다관능성의 폴리올을 40∼80℃의 온도범위에서 반응시켜 NCO기 함량이 11∼25%인 부분적 프레폴리머를 제조하는 단계 ; (나) 폴리올에 발포제, 아민계 촉매, 충진제, 및 항균처리제 및/또는 향료를 첨가하여 혼합 폴리올을 제조하는 단계 ; 및 (다) 상기 (가)단계의 프레폴리머와 상기 (나)단계의 혼합 폴리올을 1 : 1∼2의 무게비로 혼합시키는 단계로 이루어 지는 것을 특징으로 하는 정형외과용 경질 폴리우레탄 폼의 제조방법.
- 제1항에 있어서, 상기 발포제가 물이며, 그 사용량이 상기 (가)단계의 폴리올과 (나)단계의 폴리올 100중량부에 대하여 0.1∼1.5중량부임을 특징으로 하는 정형외과용 경질 폴리우레탄 폼의 제조방법.
- 제1항에 있어서, 상기 아민계 촉매가 트리에틸렌디아민(TEDA), 디메틸에탄올아민(DMEA), 및/또는 트리에탄올아민(TEOA)이며, 그 사용량이 상기 (가)단계의 폴리올과 (나)단계의 폴리올 100중량부에 대하여 0.1∼2중량부임을 특징으로 하는 정형외과용 경질 폴리우레탄 폼의 제조방법.
- 제1항에 있어서, 상기 (다)단계 혼합물의 혼합점도가 5,000∼20,000cps임을 특징으로 하는 정형외과용 경질 폴리우레탄 폼의 제조방법.
- 제1항에 있어서, 상기 충진제가 TiO2, CaO, CaCO3, 또는 SiO2이며, 그 사용량이 상기 (가)단계의 폴리올과 (나)단계의 폴리올 100중량부에 대하여 1∼60중량부임을 특징으로 하는 정형외과용 경질 폴리우레탄 폼의 제조방법.
- 메틸렌디이소시아네이트 또는 변성-메틸렌디이소시아네이트에 3∼8의 다관능성의 폴리올을 40∼80℃의 온도범위에서 반응시켜 제조된 NCO기 함량이 11∼25%인 부분적 프레폴리머와 폴리올에 발포제, 아민계 촉매, 충진제, 및 항균처리제 및/또는 향료를 첨가하여 제조된 혼합 폴리올을 1 : 1∼2의 무게비로 혼합시켜 제조된 폴리우레탄 폼의 경도(C-type)가 90∼95%이고, 밀도가 0.20∼0.35kg/㎥이며, 압축강도가 7kg/㎠이상이고, 흡습성이 1±0.1%이며, 및 96%이상의 치수안정성을 갖는 것을 특징으로 하는 정형외과용 경질 폴리우레탄 폼.
- 제6항에 있어서, 상기 폴리우레탄 폼이 5,000-20,000cps의 혼합점도, 3∼5분의 반응경화시간 및 15∼30분의 작업경화시간을 갖는 것을 특징으로 하는 정형외과용 경질 폴리우레탄 폼.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/862,008 US5272128A (en) | 1992-04-01 | 1992-04-01 | Phosphosulfonate herbicides |
US862,008 | 1992-04-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR970021120A true KR970021120A (ko) | 1997-05-28 |
KR100219421B1 KR100219421B1 (ko) | 1999-10-01 |
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Application Number | Title | Priority Date | Filing Date |
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KR1019960047929A KR100219421B1 (ko) | 1992-04-01 | 1996-10-24 | 정형외과용 경질 폴리우레탄 폼 및 이의 제조방법 |
Country Status (3)
Country | Link |
---|---|
US (2) | US5272128A (ko) |
KR (1) | KR100219421B1 (ko) |
TW (1) | TW215092B (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100448091B1 (ko) * | 2001-09-13 | 2004-09-08 | 백철균 | 항균 폴리우레탄 폼의 제조방법 |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5731299A (en) * | 1992-05-29 | 1998-03-24 | The Procter & Gamble Company | Phosphonosulfonate compounds, pharmaceutical compositions, and methods for treating abnormal calcium and phosphate metabolism |
US5470845A (en) * | 1992-10-28 | 1995-11-28 | Bristol-Myers Squibb Company | Methods of using α-phosphonosulfonate squalene synthetase inhibitors including the treatment of atherosclerosis and hypercholesterolemia |
US5693590A (en) * | 1994-08-30 | 1997-12-02 | Rohm And Haas Company | Compositions containing phosphosulfonate herbicides and dichloroacetamide safeners |
DE69505216T2 (de) | 1994-08-30 | 1999-06-17 | Rohm And Haas Co., Philadelphia, Pa. | Zusammensetzungen aus Phosphosulphonat-Herbizide und Dichloracetamide-Safener und Verwendungsmethoden |
IL115499A (en) * | 1994-10-18 | 1999-12-22 | Rohm & Haas | Preparation of 2,6-disubstituted benzensulfonate and certain derivatives thereof |
DK0877745T3 (da) * | 1996-09-24 | 2001-11-05 | Dow Agrosciences Llc | N-([1,2,4]triazoloazinyl)benzensulfonamid- og pyridinsulfonamidforbindelser og deres anvendelse som herbicider |
KR20010001279A (ko) * | 1999-06-03 | 2001-01-05 | 김형순 | 정형외과용 캐스팅 테이프 및 그 제조방법 |
TWI287547B (en) * | 2000-06-14 | 2007-10-01 | Dow Agrosciences Llc | Process for the selective deprotonation and functionalization of 3-substituted benzotrifluorides |
US6441229B1 (en) | 2000-06-23 | 2002-08-27 | Phillips Petroleum Company | Process for the preparation of higher-alkane sulfonyl halides |
KR100785232B1 (ko) | 2006-06-15 | 2007-12-11 | 남두석 | 치과용 항균 석고 조성물 및 그 제조방법 |
US8198341B2 (en) | 2008-12-18 | 2012-06-12 | Icl-Ip America Inc. | Method of making hydroxymethylphosphonate, polyurethane foam-forming compositions, polyurethane foam and articles made therefrom |
WO2011157663A1 (de) | 2010-06-15 | 2011-12-22 | Bayer Cropscience Ag | Neue ortho-substituierte arylamid-derivate |
WO2014062313A1 (en) | 2012-10-17 | 2014-04-24 | Icl-Ip America Inc. | Method of making hydroxymethylphosphonate, polyurethane foam-forming compositions, polyurethane foam and articles made therefrom |
CN103848866A (zh) * | 2012-12-04 | 2014-06-11 | 上海医药工业研究院 | 制备磺酰氧甲基膦酸二乙酯类化合物的方法 |
CN104341326A (zh) * | 2013-08-08 | 2015-02-11 | 天津诺维康生物技术有限公司 | 2-取代基-6-三氟甲基苯磺酰氯的制备方法 |
US9815256B2 (en) | 2014-06-09 | 2017-11-14 | Johns Manville | Foam boards including non-halogenated fire retardants |
US9528269B2 (en) | 2014-06-09 | 2016-12-27 | Johns Manville | Roofing systems and roofing boards with non-halogenated fire retardant |
US9523195B2 (en) | 2014-06-09 | 2016-12-20 | Johns Manville | Wall insulation boards with non-halogenated fire retardant and insulated wall systems |
US9815966B2 (en) | 2014-07-18 | 2017-11-14 | Johns Manville | Spray foams containing non-halogenated fire retardants |
CN109053799B (zh) * | 2018-08-31 | 2021-01-08 | 乐平市赛复乐医药化工有限公司 | 一种对甲苯磺酰氧甲基膦酸二乙酯的合成方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1509068A (en) * | 1974-05-27 | 1978-04-26 | Mitsubishi Petrochemical Co | Phosphonic and thiophosphonic acid derivatives and their use as plant growth regulants |
US4740608A (en) * | 1985-10-09 | 1988-04-26 | Monsanto Company | (Phosphonomethyl)trifluoromethyl sulfonates |
-
1992
- 1992-04-01 US US07/862,008 patent/US5272128A/en not_active Expired - Fee Related
- 1992-05-14 TW TW081103719A patent/TW215092B/zh active
-
1993
- 1993-09-22 US US08/125,379 patent/US5500405A/en not_active Expired - Fee Related
-
1996
- 1996-10-24 KR KR1019960047929A patent/KR100219421B1/ko not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100448091B1 (ko) * | 2001-09-13 | 2004-09-08 | 백철균 | 항균 폴리우레탄 폼의 제조방법 |
Also Published As
Publication number | Publication date |
---|---|
US5272128A (en) | 1993-12-21 |
US5500405A (en) | 1996-03-19 |
KR100219421B1 (ko) | 1999-10-01 |
TW215092B (ko) | 1993-10-21 |
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