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WO2008133269A1 - Liquide ionique et agent de traitement de polymère comprenant le liquide ionique - Google Patents

Liquide ionique et agent de traitement de polymère comprenant le liquide ionique Download PDF

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Publication number
WO2008133269A1
WO2008133269A1 PCT/JP2008/057836 JP2008057836W WO2008133269A1 WO 2008133269 A1 WO2008133269 A1 WO 2008133269A1 JP 2008057836 W JP2008057836 W JP 2008057836W WO 2008133269 A1 WO2008133269 A1 WO 2008133269A1
Authority
WO
WIPO (PCT)
Prior art keywords
ionic liquid
group
formula
nitrogen atom
represented
Prior art date
Application number
PCT/JP2008/057836
Other languages
English (en)
Japanese (ja)
Inventor
Hiroyuki Ohno
Yukinobu Fukaya
Gen Masuda
Yuji Kubota
Original Assignee
Tokyo University Of Agriculture And Technology
Nisshinbo Industries, Inc.
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.)
Filing date
Publication date
Application filed by Tokyo University Of Agriculture And Technology, Nisshinbo Industries, Inc. filed Critical Tokyo University Of Agriculture And Technology
Priority to JP2009511883A priority Critical patent/JP5339452B2/ja
Publication of WO2008133269A1 publication Critical patent/WO2008133269A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
    • C07C217/08—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom
    • 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
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/60—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to ring nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • 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
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
    • C—CHEMISTRY; METALLURGY
    • 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
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/141—Esters of phosphorous acids
    • C07F9/1411—Esters of phosphorous acids with hydroxyalkyl compounds with further substituents on alkyl
    • C—CHEMISTRY; METALLURGY
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

L'invention porte sur un liquide ionique comprenant un cation ayant un atome d'azote quaternaire et un groupe alcoxyalkyle sur l'atome d'azote (à savoir le cation représenté par la formule (1)) et un ion représenté par la formule : (CH3O)(R)PO2- [où R représente un atome d'hydrogène, un groupe méthyle ou un groupe méthoxy]. Le liquide ionique peut dissoudre différents polymères comprenant des polymères naturels à une température se situant aux alentours de la température ambiante, il présente une viscosité relativement faible, a une bonne propriété de manipulation comme liquide et peut traiter une matière d'intérêt de façon satisfaisante. R1R2R3R4N+ (1) dans laquelle R1 à R4 représentent indépendamment un groupe alkyle linéaire ou ramifié ayant 1 à 12 atomes de carbone, un groupe alcoxyalkyle représenté par la formule: -(CH2)n-OR5 [dans laquelle R5 représente un groupe méthyle ou un groupe éthyle; et n représente un nombre de 1 ou 2], ou similaire, à la condition qu'au moins l'un parmi R1 à R4 représente le groupe alcoxyalkyle mentionné ci-dessus, et n'importe quels deux groupes parmi R1 à R4 et un atome d'azote peuvent ensemble former un cycle.
PCT/JP2008/057836 2007-04-24 2008-04-23 Liquide ionique et agent de traitement de polymère comprenant le liquide ionique WO2008133269A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009511883A JP5339452B2 (ja) 2007-04-24 2008-04-23 イオン液体およびこのイオン液体からなるポリマー処理剤

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007-114018 2007-04-24
JP2007114018 2007-04-24

Publications (1)

Publication Number Publication Date
WO2008133269A1 true WO2008133269A1 (fr) 2008-11-06

Family

ID=39925718

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/057836 WO2008133269A1 (fr) 2007-04-24 2008-04-23 Liquide ionique et agent de traitement de polymère comprenant le liquide ionique

Country Status (2)

Country Link
JP (1) JP5339452B2 (fr)
WO (1) WO2008133269A1 (fr)

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010120268A1 (fr) * 2009-04-15 2010-10-21 Eastman Chemical Company Esters de cellulose à substitution régiosélective produits au moyen d'un procédé faisant appel à un liquide ionique à base d'alkylphosphate de tétraalkylammonium, et produits obtenus à partir de ceux-ci
US7919631B2 (en) 2007-02-14 2011-04-05 Eastman Chemical Company Production of ionic liquids
WO2011048608A2 (fr) 2009-10-07 2011-04-28 Grasim Industries Limited Procédé de fabrication de fibres cellulosiques de faible fibrillation
WO2011048609A2 (fr) 2009-10-07 2011-04-28 Grasim Industries Limited Procédé de fabrication de fibres cellulosiques de faible fibrillation
JP2011214003A (ja) * 2010-03-19 2011-10-27 Kaneka Corp セルロース多孔質粒子の製造方法
JP2012001459A (ja) * 2010-06-15 2012-01-05 Sanyo Chem Ind Ltd リン酸ジエステル塩の製造方法
WO2012008401A1 (fr) * 2010-07-12 2012-01-19 株式会社ブリヂストン Procédé pour la production de fibres de cellulose purifiée
US8158777B2 (en) 2008-02-13 2012-04-17 Eastman Chemical Company Cellulose esters and their production in halogenated ionic liquids
JP2012087202A (ja) * 2010-10-19 2012-05-10 Jsr Corp セルロース粒子の製造方法、及び、セルロース粒子
JP2012086154A (ja) * 2010-10-20 2012-05-10 Kanazawa Univ バイオマスの前処理方法
US8188267B2 (en) 2008-02-13 2012-05-29 Eastman Chemical Company Treatment of cellulose esters
WO2012081616A1 (fr) * 2010-12-14 2012-06-21 Jsr株式会社 Procédé de production de particules de polymère, et particules de polymère
JP2012126797A (ja) * 2010-12-14 2012-07-05 Jsr Corp 多糖複合粒子の製造方法、及び、多糖複合粒子
JP2012126796A (ja) * 2010-12-14 2012-07-05 Jsr Corp 架橋高分子粒子の製造方法、及び、架橋高分子粒子
JP2012144441A (ja) * 2011-01-06 2012-08-02 Idemitsu Kosan Co Ltd イオン液体、イオン液体の精製方法、およびセルロース系バイオマスの処理方法
US8354525B2 (en) 2008-02-13 2013-01-15 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom
US8729253B2 (en) 2011-04-13 2014-05-20 Eastman Chemical Company Cellulose ester optical films
US9777074B2 (en) 2008-02-13 2017-10-03 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom
US9834516B2 (en) 2007-02-14 2017-12-05 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom
US10174129B2 (en) 2007-02-14 2019-01-08 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom
WO2022181381A1 (fr) * 2021-02-25 2022-09-01 ミヨシ油脂株式会社 Sel d'ammonium organique ayant un anion phosphonate ou phosphinate, et composition qui est capable de former ledit sel

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8431319B2 (en) * 2011-03-22 2013-04-30 Xerox Corporation Toner wash comprising ionic liquid

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JP4011830B2 (ja) * 2000-06-20 2007-11-21 独立行政法人科学技術振興機構 Ｎ−アルコキシアルキルイミダゾリウム塩、該イミダゾリウム塩からなるイオン液体ならびにイオン性ゲル
CA2598156C (fr) * 2002-08-16 2011-02-08 Cytec Canada Inc. Sels de phosphonium et sels d'imidazolium et methodes pour leur preparation
WO2007049485A1 (fr) * 2005-10-25 2007-05-03 Nisshinbo Industries, Inc. Procede de production d’une solution de cellulose, solution de cellulose et procede de production de cellulose regeneree
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Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2486079A1 (fr) * 1980-07-07 1982-01-08 Rhone Poulenc Agrochimie Sels quaternaires d'alcoyl-1-imidazolium de l'acide phosphoreux ou ses monoesters, procedes pour les preparer et compositions fongicides les contenant
JP2005506401A (ja) * 2001-10-03 2005-03-03 ザ ユニヴァーシティー オブ アラバマ イオン性液体を用いたセルロースの溶解及びプロセッシング
JP2005530910A (ja) * 2002-06-28 2005-10-13 ザ プロクター アンド ギャンブル カンパニー イオン性液体系製品及びその使用方法

Non-Patent Citations (1)

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Title
KUHLMANN E. ET AL.: "Imidazolium Dialkylphosphates - a Class of Versatile, Halogen-Free and Hydrolytically Stable Ionic Liquids", GREEN CHEMISTRY, vol. 9, March 2007 (2007-03-01), pages 233 - 242, XP009123190, DOI: doi:10.1039/b611974c *

Cited By (46)

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US8148518B2 (en) 2007-02-14 2012-04-03 Eastman Chemical Company Cellulose esters and their production in carboxylated ionic liquids
US10174129B2 (en) 2007-02-14 2019-01-08 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom
US7919631B2 (en) 2007-02-14 2011-04-05 Eastman Chemical Company Production of ionic liquids
US9834516B2 (en) 2007-02-14 2017-12-05 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom
US8153782B2 (en) 2007-02-14 2012-04-10 Eastman Chemical Company Reformation of ionic liquids
US8273872B2 (en) 2008-02-13 2012-09-25 Eastman Chemical Company Cellulose esters and their production in halogenated ionic liquids
US8158777B2 (en) 2008-02-13 2012-04-17 Eastman Chemical Company Cellulose esters and their production in halogenated ionic liquids
US9777074B2 (en) 2008-02-13 2017-10-03 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom
US9175096B2 (en) 2008-02-13 2015-11-03 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom
US9156918B2 (en) 2008-02-13 2015-10-13 Eastman Chemical Company Treatment of cellulose esters
US8354525B2 (en) 2008-02-13 2013-01-15 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom
US8188267B2 (en) 2008-02-13 2012-05-29 Eastman Chemical Company Treatment of cellulose esters
CN102459350A (zh) * 2009-04-15 2012-05-16 伊士曼化工公司 包含烷基磷酸四烷基铵的纤维素溶液和由其制成的产品
US9926384B2 (en) 2009-04-15 2018-03-27 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a tetraalkylammonium alkylphosphate ionic liquid process and products produced therefrom
US8871924B2 (en) 2009-04-15 2014-10-28 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a tetraalkylammonium alkylphosphate ionic liquid process and products produced therefrom
EP3216806A1 (fr) * 2009-04-15 2017-09-13 Eastman Chemical Company Esters de cellulose à substitution régiosélective produits au moyen d'un procédé faisant appel à un liquide ionique à base d'alkylphosphate de tétraalkylammonium et produits ainsi obtenus
US8067488B2 (en) 2009-04-15 2011-11-29 Eastman Chemical Company Cellulose solutions comprising tetraalkylammonium alkylphosphate and products produced therefrom
WO2010120269A1 (fr) * 2009-04-15 2010-10-21 Eastman Chemical Company Solutions de cellulose comprenant un alkylphosphate de tétraalkylammonium et produits obtenus à partir de celles-ci
KR101673640B1 (ko) * 2009-04-15 2016-11-07 이스트만 케미칼 컴파니 테트라알킬암모늄 알킬포스페이트 이온성 액체 공정으로 생산된 위치선택적으로 치환된 셀룰로스 에스테르, 및 이로부터 생산된 제품
KR20120005032A (ko) * 2009-04-15 2012-01-13 이스트만 케미칼 컴파니 테트라알킬암모늄 알킬포스페이트 이온성 액체 공정으로 생산된 위치선택적으로 치환된 셀룰로스 에스테르, 및 이로부터 생산된 제품
CN102459349B (zh) * 2009-04-15 2014-05-14 伊士曼化工公司 在烷基磷酸四烷基铵离子液体法中制成的区域选择性取代的纤维素酯和由其制成的产品
US8524887B2 (en) 2009-04-15 2013-09-03 Eastman Chemical Company Regioselectively substituted cellulose esters produced in a tetraalkylammonium alkylphosphate ionic liquid process and products produced therefrom
WO2010120268A1 (fr) * 2009-04-15 2010-10-21 Eastman Chemical Company Esters de cellulose à substitution régiosélective produits au moyen d'un procédé faisant appel à un liquide ionique à base d'alkylphosphate de tétraalkylammonium, et produits obtenus à partir de ceux-ci
JP2012524145A (ja) * 2009-04-15 2012-10-11 イーストマン ケミカル カンパニー テトラアルキルアンモニウムアルキルホスフェートを含むセルロース溶液およびそれから製造される製品
WO2011048609A2 (fr) 2009-10-07 2011-04-28 Grasim Industries Limited Procédé de fabrication de fibres cellulosiques de faible fibrillation
US8952146B2 (en) 2009-10-07 2015-02-10 Grasim Industries Limited Process for manufacturing low-fibrillating cellulosic fiber
WO2011048608A2 (fr) 2009-10-07 2011-04-28 Grasim Industries Limited Procédé de fabrication de fibres cellulosiques de faible fibrillation
JP2011214003A (ja) * 2010-03-19 2011-10-27 Kaneka Corp セルロース多孔質粒子の製造方法
JP2012001459A (ja) * 2010-06-15 2012-01-05 Sanyo Chem Ind Ltd リン酸ジエステル塩の製造方法
WO2012008401A1 (fr) * 2010-07-12 2012-01-19 株式会社ブリヂストン Procédé pour la production de fibres de cellulose purifiée
JP2012021048A (ja) * 2010-07-12 2012-02-02 Bridgestone Corp 精製セルロース繊維の製造方法
JP2012087202A (ja) * 2010-10-19 2012-05-10 Jsr Corp セルロース粒子の製造方法、及び、セルロース粒子
JP2012086154A (ja) * 2010-10-20 2012-05-10 Kanazawa Univ バイオマスの前処理方法
JP2012126796A (ja) * 2010-12-14 2012-07-05 Jsr Corp 架橋高分子粒子の製造方法、及び、架橋高分子粒子
JP2012126797A (ja) * 2010-12-14 2012-07-05 Jsr Corp 多糖複合粒子の製造方法、及び、多糖複合粒子
US9352298B2 (en) 2010-12-14 2016-05-31 Jsr Corporation Method for producing polymer particles, and polymer particles
WO2012081616A1 (fr) * 2010-12-14 2012-06-21 Jsr株式会社 Procédé de production de particules de polymère, et particules de polymère
JP2012144441A (ja) * 2011-01-06 2012-08-02 Idemitsu Kosan Co Ltd イオン液体、イオン液体の精製方法、およびセルロース系バイオマスの処理方法
US9796791B2 (en) 2011-04-13 2017-10-24 Eastman Chemical Company Cellulose ester optical films
US9096691B2 (en) 2011-04-13 2015-08-04 Eastman Chemical Company Cellulose ester optical films
US9975967B2 (en) 2011-04-13 2018-05-22 Eastman Chemical Company Cellulose ester optical films
US8729253B2 (en) 2011-04-13 2014-05-20 Eastman Chemical Company Cellulose ester optical films
US10494447B2 (en) 2011-04-13 2019-12-03 Eastman Chemical Company Cellulose ester optical films
US10836835B2 (en) 2011-04-13 2020-11-17 Eastman Chemical Company Cellulose ester optical films
WO2022181381A1 (fr) * 2021-02-25 2022-09-01 ミヨシ油脂株式会社 Sel d'ammonium organique ayant un anion phosphonate ou phosphinate, et composition qui est capable de former ledit sel
JP2022129896A (ja) * 2021-02-25 2022-09-06 ミヨシ油脂株式会社 ホスホン酸又はホスフィン酸アニオンを有する有機アンモニウム塩並びに当該塩を形成し得る配合物

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JP5339452B2 (ja) 2013-11-13
JPWO2008133269A1 (ja) 2010-07-29

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