OA10667A - Procédé de fabrication de nouveaux polymères à base d'huile de coquille de noix de cajou et les produits qui en résultent - Google Patents

Procédé de fabrication de nouveaux polymères à base d'huile de coquille de noix de cajou et les produits qui en résultent Download PDF

Info

Publication number: OA10667A
Authority: OA; OAPI
Prior art keywords: hcnc; component; small amount; polyisocyanate; manufacturing
Prior art date: 1995-08-21

Application number

OA9800024A

Other languages

English (en)

French (fr)

Inventor

Martin Ernst Stielau

Original Assignee

Martin Ernst Stielau

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.)

1995-08-21

Filing date

1998-02-23

Publication date

2002-09-25

1995-08-21 Priority claimed from PT10176195A external-priority patent/PT101761B/pt

1996-04-04 Priority claimed from PT10186396A external-priority patent/PT101863A/pt

1998-02-23 Application filed by Martin Ernst Stielau filed Critical Martin Ernst Stielau

2002-09-25 Publication of OA10667A publication Critical patent/OA10667A/fr

Links

238000000034 method Methods 0.000 title claims abstract description 11
229920000642 polymer Polymers 0.000 title claims description 5
244000226021 Anacardium occidentale Species 0.000 title abstract description 4
235000020226 cashew nut Nutrition 0.000 title abstract description 4
239000010466 nut oil Substances 0.000 title 1
229920001228 polyisocyanate Polymers 0.000 claims abstract description 12
239000005056 polyisocyanate Substances 0.000 claims abstract description 12
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 11
239000012948 isocyanate Substances 0.000 claims abstract description 6
150000002513 isocyanates Chemical class 0.000 claims abstract description 6
HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 claims description 18
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
238000004519 manufacturing process Methods 0.000 claims description 8
238000010438 heat treatment Methods 0.000 claims description 7
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
239000006260 foam Substances 0.000 claims description 6
150000001299 aldehydes Chemical class 0.000 claims description 4
230000000903 blocking effect Effects 0.000 claims description 2
239000000126 substance Substances 0.000 claims description 2
239000004033 plastic Substances 0.000 claims 2
230000005494 condensation Effects 0.000 claims 1
238000009833 condensation Methods 0.000 claims 1
238000006114 decarboxylation reaction Methods 0.000 claims 1
239000000463 material Substances 0.000 claims 1
238000013021 overheating Methods 0.000 claims 1
238000010792 warming Methods 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 13
235000014113 dietary fatty acids Nutrition 0.000 abstract description 4
229930195729 fatty acid Natural products 0.000 abstract description 4
239000000194 fatty acid Substances 0.000 abstract description 4
150000004665 fatty acids Chemical class 0.000 abstract description 4
239000002253 acid Substances 0.000 abstract 1
125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
239000000047 product Substances 0.000 description 12
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KVVSCMOUFCNCGX-UHFFFAOYSA-N cardol Chemical compound CCCCCCCCCCCCCCCC1=CC(O)=CC(O)=C1 KVVSCMOUFCNCGX-UHFFFAOYSA-N 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
239000003292 glue Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
235000014571 nuts Nutrition 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
KAOMOVYHGLSFHQ-UTOQUPLUSA-N anacardic acid Chemical compound CCC\C=C/C\C=C/CCCCCCCC1=CC=CC(O)=C1C(O)=O KAOMOVYHGLSFHQ-UTOQUPLUSA-N 0.000 description 1
235000014398 anacardic acid Nutrition 0.000 description 1
ADFWQBGTDJIESE-UHFFFAOYSA-N anacardic acid 15:0 Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1C(O)=O ADFWQBGTDJIESE-UHFFFAOYSA-N 0.000 description 1
229920005601 base polymer Polymers 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
UFMJCOLGRWKUKO-UHFFFAOYSA-N cardol diene Natural products CCCC=CCC=CCCCCCCCC1=CC(O)=CC(O)=C1 UFMJCOLGRWKUKO-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
230000000911 decarboxylating effect Effects 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
238000005530 etching Methods 0.000 description 1
235000013305 food Nutrition 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
238000011002 quantification Methods 0.000 description 1
238000009877 rendering Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
229920002725 thermoplastic elastomer Polymers 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
- C08G18/80—Masked polyisocyanates
- 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
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3215—Polyhydroxy compounds containing aromatic groups or benzoquinone 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
- C08G18/28—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
- C08G18/36—Hydroxylated esters of higher fatty acids
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/54—Polycondensates of aldehydes
- C08G18/542—Polycondensates of aldehydes with phenols

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Compounds Of Unknown Constitution (AREA)

OA9800024A 1995-08-21 1998-02-23 Procédé de fabrication de nouveaux polymères à base d'huile de coquille de noix de cajou et les produits qui en résultent OA10667A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
PT10176195A PT101761B (pt)	1995-08-21	1995-08-21	Processo de fabrico de novos polimeros a base de oleo da casca de castanha de caju
PT10186396A PT101863A (pt)	1996-04-04	1996-04-04	Processo de fabrico de uma espuma rigida a base de oleo da casca da castanha de caju

Publications (1)

Publication Number	Publication Date
OA10667A true OA10667A (fr)	2002-09-25

Family

ID=26653454

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
OA9800024A OA10667A (fr)	1995-08-21	1998-02-23	Procédé de fabrication de nouveaux polymères à base d'huile de coquille de noix de cajou et les produits qui en résultent

Country Status (10)

Country	Link
US (1)	US6051623A (de)
EP (1)	EP0846136B1 (de)
JP (1)	JPH11512122A (de)
AP (1)	AP9801213A0 (de)
AT (1)	ATE198899T1 (de)
AU (1)	AU704532B2 (de)
BR (1)	BR9610395A (de)
DE (1)	DE69611679D1 (de)
OA (1)	OA10667A (de)
WO (1)	WO1997007150A1 (de)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6962636B2 (en)	1998-09-17	2005-11-08	Urethane Soy Systems Company, Inc.	Method of producing a bio-based carpet material
US7595094B2 (en)	1998-09-17	2009-09-29	Urethane Soy Systems, Co.	Vegetable oil-based coating and method for application
US6979477B2 (en)	2000-09-06	2005-12-27	Urethane Soy Systems Company	Vegetable oil-based coating and method for application
US7063877B2 (en)	1998-09-17	2006-06-20	Urethane Soy Systems Company, Inc.	Bio-based carpet material
US20020058774A1 (en)	2000-09-06	2002-05-16	Kurth Thomas M.	Transesterified polyol having selectable and increased functionality and urethane material products formed using the polyol
US20030191274A1 (en)	2001-10-10	2003-10-09	Kurth Thomas M.	Oxylated vegetable-based polyol having increased functionality and urethane material formed using the polyol
US6180686B1 (en)	1998-09-17	2001-01-30	Thomas M. Kurth	Cellular plastic material
DE10004427A1 (de) *	2000-02-02	2001-10-04	Martin Stielau	Verfahren zur Herstellung von Polyurethan
WO2001070842A2 (en) *	2000-03-20	2001-09-27	Kt Holdings, Llc	Polyurethane foams
US7244772B2 (en) *	2004-06-30	2007-07-17	Council Of Scientific And Industrial Research	Process for preparing polyurethane polyol and rigid foams therefrom
DE602004020122D1 (de) *	2004-06-30	2009-04-30	Council Scient Ind Res	Verfahren zur herstellung von polyurethanpolyol und hartschaumstoffen daraus aus cardanol
CN101218272A (zh)	2005-03-03	2008-07-09	南达科他大豆处理机有限公司	采用氧化方法从植物油衍生的新型多元醇
WO2007077564A1 (en) *	2005-12-30	2007-07-12	Council Of Scientific And Industrial Research	Process for synthesis of telechelic urethane acrylate uv curable pre-polymeric materials
US7828991B2 (en) *	2006-12-08	2010-11-09	Bayer Materialscience Llc	Polyether polyols based on cashew nutshell liquid and flexible foams
TR201903021T4 (tr) *	2013-06-25	2019-03-21	Covestro Llc	Geliştirilmiş kaplama yapışmasına sahip ürünlerin üretimine yönelik poliüretan pultruzyon formülasyonları ve bunlardan üretilen ürünler.
US10308833B2 (en)	2013-11-27	2019-06-04	Dow Global Technologies Llc	Curable polyurethane coating composition and method of preparing the same
JP2015117275A (ja) *	2013-12-17	2015-06-25	住化バイエルウレタン株式会社	ポリウレタン樹脂用原料としてのカシューナッツ殻液の使用
JP6656796B2 (ja) *	2014-08-27	2020-03-04	コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏＤｅｕｔｓｃｈｌａｎｄＡｇ	ポリイソシアヌレートフォーム原料としてのカシューナッツ殻液の使用
JP6683696B2 (ja)	2014-11-05	2020-04-22	ダウグローバルテクノロジーズエルエルシー	難燃性ポリオール
JP2023092020A (ja) *	2021-12-21	2023-07-03	株式会社イノアックコーポレーション	ポリウレタンフォームとその製造方法及びシール材

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4301254A (en) *	1980-03-14	1981-11-17	Blount David H	Process for the production of poly(aldehyde aminosilicon acid) resinous products and foams
JPS604840A (ja) *	1983-06-22	1985-01-11	Agency Of Ind Science & Technol	流体検出装置
JPS60212453A (ja) *	1984-04-09	1985-10-24	Kanegafuchi Chem Ind Co Ltd	硬化性樹脂組成物
JPH06102770B2 (ja) *	1988-02-10	1994-12-14	斎藤株式会社	カシュー樹脂変性ポリウレタン樹脂塗料の製造方法

1996
- 1996-08-20 JP JP9509189A patent/JPH11512122A/ja active Pending
- 1996-08-20 AP APAP/P/1998/001213A patent/AP9801213A0/en unknown
- 1996-08-20 EP EP96927951A patent/EP0846136B1/de not_active Expired - Lifetime
- 1996-08-20 AT AT96927951T patent/ATE198899T1/de not_active IP Right Cessation
- 1996-08-20 WO PCT/PT1996/000007 patent/WO1997007150A1/fr not_active Ceased
- 1996-08-20 AU AU67583/96A patent/AU704532B2/en not_active Ceased
- 1996-08-20 BR BR9610395-7A patent/BR9610395A/pt not_active Application Discontinuation
- 1996-08-20 DE DE69611679T patent/DE69611679D1/de not_active Expired - Lifetime
- 1996-08-20 US US09/011,894 patent/US6051623A/en not_active Expired - Fee Related
1998
- 1998-02-23 OA OA9800024A patent/OA10667A/fr unknown

Also Published As

Publication number	Publication date
WO1997007150A1 (fr)	1997-02-27
US6051623A (en)	2000-04-18
EP0846136A1 (de)	1998-06-10
AU6758396A (en)	1997-03-12
JPH11512122A (ja)	1999-10-19
ATE198899T1 (de)	2001-02-15
AU704532B2 (en)	1999-04-29
AP9801213A0 (en)	1998-03-31
BR9610395A (pt)	2000-05-09
EP0846136B1 (de)	2001-01-24
DE69611679D1 (de)	2001-03-01

Publication	Publication Date	Title
OA10667A (fr)	2002-09-25	Procédé de fabrication de nouveaux polymères à base d'huile de coquille de noix de cajou et les produits qui en résultent
EP0219399B1 (de)	1990-05-30	Verfahren zur Herstellung von wässrigen Bitumen-Polyurethan-Dispersionsmassen
FR2650288A1 (fr)	1991-02-01	Adhesif thermofusible durcissant a l'humidite
FR2459808A1 (fr)	1981-01-16	Polyoxypropylene-urethanes, leur preparation et leurs utilisations
FR2516090A1 (fr)	1983-05-13	Composition de resine thermodurcissable comportant un polyester oligomere couple a un polyisocyanate organique
EP0259233B1 (de)	1991-09-25	Verfahren zur Herstellung von Polyisocyanaten mit Biuretstruktur
FR2518555A1 (fr)	1983-06-24	Compositions de resines de polyurethanes a durcisseurs latents
FR2629088A1 (fr)	1989-09-29	Polyamide-imides aromatiques fonctionnalises par des groupes maleimido, un procede pour leur preparation et leur emploi pour notamment preparer des polymeres reticules
EP0156665B1 (de)	1988-05-18	Verfahren zur Verbesserung der Hydrolysebeständigkeit von gesättigten Urethan-Elastomeren, Zusammensetzungen zur Erledigung dieses Verfahrens sowieso hergestellte Produkte
EP0922068A1 (de)	1999-06-16	Verwendung von cashewnussschalenöl im recycling von kautschuk und wärmehärtbaren kunststoffen
CH398978A (fr)	1966-03-15	Procédé de préparation de substances polymérisées
EP0135443B1 (de)	1987-11-11	Hitzehärtbare Polymere und Prepolymere, erhältlich durch Polykondensation von alkyliertem Pyridin und aromatische hydroxylierte Monoaldehyden
FR2610938A1 (fr)	1988-08-19	Compositions de polybenzhydrolimides terminees par des groupements a insaturation ethylenique, les polyimides reticules obtenus par leur polymerisation thermique et l'utilisation de ces compositions
FR2596053A1 (fr)	1987-09-25	Procede pour la preparation de copolymeres sequences polyurethanne/polyamide pouvant subir une mise en oeuvre pour thermoplastique, et leur utilisation
BE637609A (de)
FR2583416A1 (fr)	1986-12-19	Composition d'aminobenzylamines.
BE539823A (de)
BE346189A (de)
BE876912A (fr)	1979-12-11	Resines phenoliques a stabilite amelioree au traitement a basse temperature
BE405311A (de)
BE581530A (de)
BE638290A (de)
CH340727A (fr)	1959-08-31	Article abrasif et procédé de fabrication de cet article
BE542230A (de)
BE829670A (fr)	1975-12-01	Polymere durci par catalyse par une amine et son procede de preparation