KR20000062381A - 알킬화 메틸올화 4,5-디히드록시-이미다졸리딘-2-온의 혼합물 - Google Patents
알킬화 메틸올화 4,5-디히드록시-이미다졸리딘-2-온의 혼합물 Download PDFInfo
- Publication number
- KR20000062381A KR20000062381A KR1019997005937A KR19997005937A KR20000062381A KR 20000062381 A KR20000062381 A KR 20000062381A KR 1019997005937 A KR1019997005937 A KR 1019997005937A KR 19997005937 A KR19997005937 A KR 19997005937A KR 20000062381 A KR20000062381 A KR 20000062381A
- Authority
- KR
- South Korea
- Prior art keywords
- glycol
- monovalent
- dmdheu
- reaction
- alcohol
- 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.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- NNTWKXKLHMTGBU-UHFFFAOYSA-N 4,5-dihydroxyimidazolidin-2-one Chemical class OC1NC(=O)NC1O NNTWKXKLHMTGBU-UHFFFAOYSA-N 0.000 title claims abstract description 16
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims abstract description 48
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 claims abstract description 22
- 238000006243 chemical reaction Methods 0.000 claims abstract description 21
- 229920005862 polyol Polymers 0.000 claims abstract description 20
- 150000003077 polyols Chemical class 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 15
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 10
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims abstract description 10
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims abstract description 8
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 claims abstract description 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 5
- 229940058015 1,3-butylene glycol Drugs 0.000 claims abstract description 4
- 235000019437 butane-1,3-diol Nutrition 0.000 claims abstract description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 44
- 239000000835 fiber Substances 0.000 claims description 16
- 229920003043 Cellulose fiber Polymers 0.000 claims description 6
- -1 C 5 alcohols Chemical class 0.000 claims description 5
- 239000004971 Cross linker Substances 0.000 claims description 5
- 239000002657 fibrous material Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 21
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 12
- 239000007787 solid Substances 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 238000006266 etherification reaction Methods 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 1
- 125000002632 imidazolidinyl group Chemical group 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000007039 two-step reaction Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/432—Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
- C07D233/40—Two or more oxygen atoms
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polyethers (AREA)
Abstract
Description
| 실시예 | LAW112ppm | 몬산토 등급md | 파단 손실% | 방출 인자 gC/kg 생성물** |
| 실시예 4 | 48 | 3 | 19 | 2 |
| 실시예 3 | 87 | 2.5 | 16 | 2 |
| 실시예 2 | 31 | 3 | 25 | 3 |
| 실시예 1 | 36 | 2.8 | 22 | 4 |
| 비교예 1 | 73 | 3.3 | 33 | 15 |
| 비교예 2 | 46 | 3 | 28 | 11 |
| 비교예 3 | 48 | 2 | 20 | 1 |
Claims (10)
- 메틸올화 4,5-디히드록시이미다졸리딘-2-온(DMDHEU)을 1가의 C1-5알코올과, 에틸렌 글리콜, 디에틸렌 글리콜, 1,2-프로필렌 글리콜, 1,3-프로필렌 글리콜, 1,2-부틸렌 글리콜, 1,3-부틸렌 글리콜, 1,4-부틸렌 글리콜, 글리세롤 및 식 HO(CH2CH2O)nH(식중, 3 ≤n ≤20)의 폴리에틸렌 글리콜로 구성된 군으로부터 선택되는 폴리올과 반응시키며, 상기 1가의 C1-5알코올 및 폴리올은 각각 DMDHEU에 대하여 0.1 내지 2.0 mol 당량의 양으로 사용하고, 상기 반응은 20℃ 내지 70℃의 온도와 1 내지 2.5의 pH에서 실행하며, 반응후 pH는 4 내지 8의 값으로 설정하는 것을 특징으로 하는 혼합된 알킬화 메틸올화 4,5-디히드록시이미다졸리딘-2-온의 혼합물의 제조 방법.
- 제1항에 있어서, 1가의 C1내지 C5알코올 및 폴리올과의 반응은 일단계 또는 이단계로 실행하는 것을 특징으로 하는 제조 방법.
- 제1항 또는 제2항에 있어서, 사용되는 1가의 C1내지 C5알코올은 메탄올이고 사용되는 폴리올은 디에틸렌 글리콜인 것을 특징으로 하는 제조 방법.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 온도는 20 내지 50℃인 것을 특징으로 하는 제조 방법.
- 제1항 내지 제4항 중 어느 한 항에 있어서, DMDHEU에 대하여, 1가의 C1내지 C5알코올은 0.7 내지 2.0 mol 당량의 양으로, 그리고 폴리올은 0.8 내지 1.4 mol 당량의 양으로 각기 사용하는 것을 특징으로 하는 제조 방법.
- 제1항 내지 제5항 중 어느 한 항에 있어서, DMDHEU에 대하여, 1가의 C1-5알코올과 폴리올을 1.7 내지 2.9 mol 당량의 양으로 함께 사용하는 것을 특징으로 하는 방법.
- 제1항 내지 제6항 중 어느 한 항에 의한 방법에 의하여 제조 가능한 혼합물.
- 제7항에 의한 혼합물을 포함하는 섬유 셀룰로스 물질을 위한 수성 가공욕.
- 셀룰로스 섬유 물질을 가공하는 데, 제7항에 의한 혼합물 또는 제8항에 의한 수성 가공욕을 사용하는 방법.
- 제9항에 있어서, 저 방출 섬유 가교결합제로서 사용하는 방법.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19654739.3 | 1996-12-30 | ||
| DE19654739A DE19654739A1 (de) | 1996-12-30 | 1996-12-30 | Gemischt-alkylierte bzw. -hydroxyalkoxyalkylierte methylolierte 4,5-Dihydroxy-imidazolidin-2-one |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20000062381A true KR20000062381A (ko) | 2000-10-25 |
Family
ID=7816415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019997005937A Ceased KR20000062381A (ko) | 1996-12-30 | 1997-12-30 | 알킬화 메틸올화 4,5-디히드록시-이미다졸리딘-2-온의 혼합물 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6265589B1 (ko) |
| EP (1) | EP0948488A1 (ko) |
| JP (1) | JP2001507355A (ko) |
| KR (1) | KR20000062381A (ko) |
| CA (1) | CA2276391A1 (ko) |
| DE (1) | DE19654739A1 (ko) |
| WO (1) | WO1998029393A1 (ko) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2324949A1 (en) * | 1998-03-24 | 1999-09-30 | Avantgarb, Llc | Modified textile and other materials and methods for their preparation |
| DE19860204A1 (de) * | 1998-12-24 | 2000-06-29 | Basf Ag | Verfahren zur Herstellung von cellulosehaltigen textilen Materialien |
| DE10246401A1 (de) | 2002-10-04 | 2004-08-05 | Georg-August-Universität Göttingen | Verfahren zur Verbesserung der Dauerhaftigkeit, Dimensionsstabilität und Oberflächenhärte eines Holzkörpers |
| DE10246400A1 (de) * | 2002-10-04 | 2004-08-05 | Georg-August-Universität Göttingen | Verfahren zur Verbesserung der Oberflächenhärte eines Holzkörpers mit einer wässrigen Lösung eines Imprägniermittels |
| DE10335673B4 (de) | 2003-08-04 | 2007-01-18 | Celanese Emulsions Gmbh | Wässrige Dispersionsklebstoffe, Verfahren zu deren Herstellung und deren Verwendung |
| DE102004031530A1 (de) * | 2004-06-29 | 2006-02-09 | Basf Ag | Verfahren zum Kolorieren von textilen Substraten, wässrige Vorbehandlungsflotten und ihre Verwendung zur Vorbehandlung von textilen Substraten |
| DE102005050658A1 (de) * | 2005-10-20 | 2007-04-26 | Basf Ag | Verfahren zur Verminderung der Absorption von Wasser und Wasserdampf und zur Erhöhung der Dimensionsstabilität von Papier und Papierprodukten und Verwendung von beschichteten Papierprodukten |
| EP2239322A1 (en) | 2009-04-07 | 2010-10-13 | Basf Se | Use of enzymes to reduce formaldehyde from formaldehyde-containing products |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3091617A (en) * | 1961-02-03 | 1963-05-28 | American Cyanamid Co | Process for preparing 4, 5-dialkoxy-1, 3-dialkyl-2-imidazolidinones |
| BE615426A (ko) * | 1961-02-03 | 1900-01-01 | ||
| CH507950A (de) * | 1968-03-14 | 1971-05-31 | Sumitomo Chemical Co | Verfahren zur Herstellung eines Kondensationsproduktes |
| US4295846A (en) * | 1980-03-18 | 1981-10-20 | Basf Aktiengesellschaft | Process for the production of formaldehyde-free finishing agents for cellulosic textiles and the use of such agents |
| US4396391B2 (en) * | 1982-06-30 | 1993-03-16 | Treating cellulose textile fabrics with dimenthylol dihydroyethyleneuree-polyol | |
| NL8701308A (nl) * | 1987-06-04 | 1989-01-02 | Dsm Resins Bv | Ureumderivaat en een harssamenstelling op basis van dit ureumderivaat. |
| US5160503A (en) * | 1989-11-13 | 1992-11-03 | West Point Pepperell | Water-soluble blends of active methylene compounds and polyhydric alcohols as formaldehyde scavengers |
| US5352372A (en) * | 1993-02-02 | 1994-10-04 | Sequa Chemicals, Inc. | Textile resins with reduced free formaldehyde |
-
1996
- 1996-12-30 DE DE19654739A patent/DE19654739A1/de not_active Withdrawn
-
1997
- 1997-12-30 KR KR1019997005937A patent/KR20000062381A/ko not_active Ceased
- 1997-12-30 JP JP52962198A patent/JP2001507355A/ja active Pending
- 1997-12-30 US US09/331,583 patent/US6265589B1/en not_active Expired - Fee Related
- 1997-12-30 CA CA002276391A patent/CA2276391A1/en not_active Abandoned
- 1997-12-30 WO PCT/EP1997/007318 patent/WO1998029393A1/de not_active Ceased
- 1997-12-30 EP EP97954477A patent/EP0948488A1/de not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| DE19654739A1 (de) | 1998-07-02 |
| WO1998029393A1 (de) | 1998-07-09 |
| JP2001507355A (ja) | 2001-06-05 |
| CA2276391A1 (en) | 1998-07-09 |
| US6265589B1 (en) | 2001-07-24 |
| EP0948488A1 (de) | 1999-10-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 19990629 Patent event code: PA01051R01D Comment text: International Patent Application |
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| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20020614 Comment text: Request for Examination of Application |
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| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20040804 Patent event code: PE09021S01D |
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| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20041020 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20040804 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |