WO1997036934A1 - Procede de fluoration de matieres cellulosiques et matieres cellulosiques fluorees - Google Patents
Procede de fluoration de matieres cellulosiques et matieres cellulosiques fluorees Download PDFInfo
- Publication number
- WO1997036934A1 WO1997036934A1 PCT/JP1997/001061 JP9701061W WO9736934A1 WO 1997036934 A1 WO1997036934 A1 WO 1997036934A1 JP 9701061 W JP9701061 W JP 9701061W WO 9736934 A1 WO9736934 A1 WO 9736934A1
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- WIPO (PCT)
- Prior art keywords
- fluorine
- group
- compound
- cellulosic material
- catalyst
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H8/00—Macromolecular compounds derived from lignocellulosic materials
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
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- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/02—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin
- D06M14/04—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin of vegetal origin, e.g. cellulose or derivatives thereof
-
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
- D06M15/256—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing fluorine
-
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
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- 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
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/10—Processes in which the treating agent is dissolved or dispersed in organic solvents; Processes for the recovery of organic solvents thereof
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
- D21C9/001—Modification of pulp properties
- D21C9/002—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives
- D21C9/005—Modification of pulp properties by chemical means; preparation of dewatered pulp, e.g. in sheet or bulk form, containing special additives organic compounds
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- 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
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/11—Oleophobic properties
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/12—Hydrophobic properties
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/45—Shrinking resistance, anti-felting properties
Definitions
- the present invention relates to a method for fluorinating a cellulose-based material and a fluorinated cellulose-based material.
- a method for obtaining a fluorinated cellulose derivative using a solvent-soluble cellulose derivative is known (see Japanese Patent Application Laid-Open No. 61-171702). This method is not practical because it cannot be applied to the treatment of ordinary wood, cotton cloth, paper, etc., and it is difficult to remove HF produced as a by-product during the reaction. It is also known that a cellulose derivative is obtained by directly reacting cellulose with a fluorine-containing compound such as trifluoroacetic acid (see Cellulose Chemistry and Technology, 16 (6). 615. (1982)). According to the reaction, despite the fact that a derivative with a high degree of substitution is obtained, the functions expected by the introduction of fluorine are not sufficiently exhibited.
- Wood is a typical lignocellulosic material, but as a method of imparting water repellency to the wood and increasing its stain resistance, fluorine-containing monomers such as heptadecafluorodecyl acrylate are incorporated into the wood. After impregnation, heating to polymerize the monomer (see Japanese Patent Application Laid-Open No. 61-86972, etc.), impregnating wood with a compound having a high fluorine-containing organic group, and heating (See Japanese Patent Application Laid-Open No. 61-1200705, etc.).
- fluorine-containing monomers such as heptadecafluorodecyl acrylate are incorporated into the wood. After impregnation, heating to polymerize the monomer (see Japanese Patent Application Laid-Open No. 61-86972, etc.), impregnating wood with a compound having a high fluorine-containing organic group, and heating (See Japanese Patent Application Laid-Open No.
- the fluorine-containing compound was expensive and uneconomical, and because it was also a polymer, it was only the surface of the wood, and the interior was not modified.
- Surface treatment method using fluorine-containing gas plasma such as tetrafluoromethane (see Journal of the Wood Society of Japan, Vol. 38, No. 1, pages 73-80, January 1992)
- fluorine-containing gas plasma such as tetrafluoromethane
- Cotton and paper which are typical cellulose and / or lignocellulosic materials, are also made of a polymer of a compound such as acrylic acid or methacrylic acid ester containing a perfluoroalkyl group, or a polymer of acrylic acid or methacrylic acid.
- Attempts to modify the surface by applying a water and oil repellent made of a copolymer with other polymerizable compounds such as esters, maleic anhydride, chlorobrene, butadiene, and methyl vinyl ketone to cotton cloth, paper, etc. are well known. However, there is no internal reforming.
- An object of the present invention is to improve the functionality of a cellulose and / or lignocellulose material by modifying not only the surface but also the inside of the cellulose and / or lignocellulose material.
- the present invention relates to a cellulose-based material selected from the group consisting of a cellulose material and a lignocellulose material, a fluorine-containing olefin compound, a fluorine-containing acrylate compound, and a fluorine-containing methacrylate compound in an organic solvent in the presence of a catalyst. From :! Provided is a method for saturating a cellulosic material by reaction with at least one type of fluorine-containing compound.
- the present invention also provides a fluorinated cellulose-based material obtained by the fluorination method.
- the reaction between the cellulose material and / or the lignocellulose material and the fluorine-containing compound is preferably an ionic reaction.
- —Crotch cellulo The ⁇ H group of the cellulose material or lignocellulose material reacts with the fluorine-containing compound.
- the cellulosic material has a fluorocarbon group (R i group or R i ′ group in the following formula).
- the cellulosic material examples include natural cellulose such as cotton and hemp, and regenerated cellulose such as pisco-rayon and copper-ammonium-rayon. Other examples include cellulose acetate and cellulose petrate. An organic acid ester having 1 to 20 carbon atoms, an alkyl ether which may have a substituent having 1 to 6 carbon atoms, such as methylcellulose, ethylcellulose, and quinprovir cellulose. Alternatively, a cellulose derivative such as an inexpensive and easily available nitrocell mouth may be used.
- lignocellulosic materials include wood, pulp, and paper, and any of these materials can be used as a raw material regardless of shape and tree type.
- wood veneer wood thin plate, ground plate, columnar body, block-like body, and plywood, laminated material, fiber board, fiber mat, chip board (wood chip) formed from these.
- wood flour particles
- any of mechanical pulp, chemical pulp and semi-chemical pulp can be used as raw materials.
- chemical pulp either salash or unsalash is acceptable.
- shape of the pulp such as chips, flakes, sheets, pulp moldings, and lumps.
- processing can be performed even in a sheet shape.
- cellulosic and / or lignocellulosic materials can also be used as raw materials in cotton blended fabrics (woven and nonwoven) or clothing.
- the organic solvent is preferably a non-protonic polar organic solvent.
- solvents are acetonitrile, dimethylformamide, dimethylacetamide, dimethylsulfoxide, hexamethylenephosphamide, monoglyme, diglyme, triglyme, tetraglyme and the like. Particularly preferred are acetonitrile, dimethylformamide and dimethylsulfoxide.
- the amount of the organic solvent may be 1 to 500 times, for example, 5 to 200 times the weight of the cellulosic material.
- the catalyst is preferably a basic catalyst, and particularly preferably one having no nucleophilicity. Electrophilic catalysts are preferred.
- the catalyst is an alkali metal or alkaline earth metal fluoride salt. Among them, KF, NaF and CsF are mentioned from the viewpoint of not decomposing and coloring the cellulose and / or lignocellulose material, and it is particularly preferable to use KF.
- the catalyst is preferably a dried one having a high activity.
- the amount of the catalyst to be added is preferably 0.5 to 20 equivalents, particularly preferably 1 to 5 equivalents, per equivalent of the ⁇ H group of the cellulose material and / or lignocellulose material.
- RfCF CF 2
- RfCF C C1F
- RfCF CH 2
- RfCH CH 2
- Rf 2 C CF 2
- Rf 2 C CH 2
- RfOCOCH CH 2
- RfOCOC (CH 3 ) CH 2
- Rf is F, Cl, polyfurfuryl O b alkyl group d-so, C physician 30 polyphenylene Ruoroarukeniru group, C, -30 of Helsingborg full O b alkoxy group or,
- R can be, for example, a perfluoroalkyl group, a perfluoroalkenyl group, a perfluoroalkoxy group, or a perfluoropolyether group.
- R f include the following.
- CF 2 C (CF 3 ) C (F) (CF 2 CF 3 )-
- (CF 3) 2 C C [CF (CF 3) 2] C (F) (CF 3) - HCF 2 CF 2 0 -,
- R 1 (CF (CF 3 ) CF20) f (CF 2 CF20) g (CF20) hR 2- (where a.b, c.d, e, f.g, h do not simultaneously become 0 0 to 10
- R and R 1 are hydrogen, halogen, or an alkoxy group having 1 to 3 carbon atoms, which may be partially or entirely fluorinated;
- R 2 is a divalent organic group having 1 to 5 carbon atoms, for example, a divalent alkyl group, a divalent alkenyl group, It is an alkyl ether group, a dihydric alkyl alcohol group, or the like, and may be partially or entirely fluorinated.
- Rf ' may be, for example, a perfluoro group.
- R 5 and RR 7 are a divalent organic group having 1 to 5 carbon atoms, for example, a divalent alkyl group, a divalent alkenyl group, a divalent alkyl ether group, a divalent alkyl alcohol group, and the like, partially or All may be fluorinated.
- the amount of the fluorine-containing compound may be 0.1 to 50 equivalents, for example, 5 to 20 equivalents, per equivalent of the 0H group of the cellulosic material.
- the reaction pressure is preferably 0 to 100 kgZcm 2 G
- the reaction temperature is preferably 0 ° C to 150 ° C.
- the reaction time is usually 1 to 120 hours. Since the reaction of the present invention can be performed in a heterogeneous system, it is not necessary to perform chemical modification (eg, esterification) of cellulose and / or lignocellulose material for dissolving in a solvent.
- the cellulosic material thus obtained is excellent in water repellency, oil repellency, antifouling property, antiseptic property, insect repellency, weather resistance, chemical resistance, oil resistance, heat resistance, dimensional stability, strength, etc. It is a new cellulosic material that has been fluorinated not only inside but also newly enhanced.
- test was performed as follows.
- the measurement sample was left in the kitchen for one month, and evaluated visually.
- the measurement sample was left outdoors for one month and evaluated visually.
- the measurement was performed using Tensilon 50 Okgf (manufactured by Orientic Co., Ltd.).
- Example 1 10 Oml autoclave in a cotton fabric (woven fabric formed from yarn of size 40) (2cm x 2cm): 0.59 g (3.64 10 "1 ⁇ 2ol), dried KF (Kurokatto F, Morita) 0.845 g (1.3 equivalents per 1 equivalent of ⁇ H group of cellulose material), 50 ml of acetonitrile, cooled to 0 ° C under nitrogen atmosphere, hexafluoropropene 16g (cellulose material (10 equivalents per 1 equivalent of H group) After the introduction of the hexafluorolob pen was completed, heat to 50 ° C once and confirm that there was no sudden heat generation. The mixture was heated to C and reacted for about 1 hour After the reaction, the sample was washed six times each with pure water and HCFC-141b, and air-dried overnight.
- KF Koreanto F, Morita
- the obtained sample was evaluated for the contact angle, the water content, and the antifouling property. The results are shown in Tables 1 and 3.
- Example 4 The same procedure as in Example 1 was repeated except that 50 ml of dimethyl sulfokind (Example 2) and 50 ml of dimethylformamide (Example 3) were used instead of acetonitrile as the solvent. The results are shown in Tables 1 and 3.
- Example 4 The same procedure as in Example 1 was repeated except that 50 ml of dimethyl sulfokind (Example 2) and 50 ml of dimethylformamide (Example 3) were used instead of acetonitrile as the solvent. The results are shown in Tables 1 and 3.
- Example 4 The same procedure as in Example 1 was repeated except that 50 ml of dimethyl sulfokind (Example 2) and 50 ml of dimethylformamide (Example 3) were used instead of acetonitrile as the solvent. The results are shown in Tables 1 and 3.
- Example 4 The same procedure as in Example 1 was repeated except that 50 ml of dimethyl sulfokind (Example 2) and 50 m
- the obtained sample was evaluated for the contact angle, the water content, and the antifouling property. The results are shown in Tables 1 and 3.
- Onil monoclave is made of lignocellulosic material, wood chips (Bematsu, size 2x1x0.6 cm): 0.59 g (3.64x10'1 ⁇ 2 ⁇ 1), dried KF (Kurokatto F, Morita Chemical Co., Ltd.) ): 0.845 g (1.3 equivalents to 1 equivalent of OH group in cellulose material), 5 acetate 5 OID 1, and cooled to 0 ° C under nitrogen atmosphere to obtain hexafluoropropene 16 g (10 equivalents per 1 equivalent of OH group of the cellulose material) were gradually introduced.
- the mixture was heated to 50 ° C once to confirm that there was no sudden heat generation, and then heated to 80 ° C and reacted for about 1 hour. After the reaction, the sample was washed six times each with pure water and HCF C-141b, and air-dried all day and night.
- the obtained sample was evaluated for contact angle, water content, antifouling property, weather resistance, and anti-vibration property. The results are shown in Tables 2-5.
- Example 5 The same procedure as in Example 5 was repeated except that 11 g of tetrafluoroethylene was used instead of hexafluoropropene as the fluorine-containing compound. The results are shown in Tables 2-5.
- Example 5 The same procedure as in Example 5 was repeated, except that NaF (0.612 g) was used instead of KF as the catalyst. The results are shown in Tables 2-5.
- Example 4 0.10 g of the same wood chip as used in Example 4 was immersed in a water / oil repellent, Unidyne TG-410 (manufactured by Daikin Industries, Ltd.) at 20 ° C for 30 minutes, and then removed (Ettsu Pickup) : 168 weight, 100, dried for 3 minutes.
- Unidyne TG-410 manufactured by Daikin Industries, Ltd.
- the obtained sample was evaluated for contact angle, water content, antifouling property, weather resistance, and anti-vibration property. The results are shown in Tables 2-5.
- a cellulose and / or lignocellulose material is reacted with at least one fluorine-containing compound selected from a fluorine-containing olefin compound, a fluorine-containing acrylate compound, and a fluorine-containing methacrylate compound to obtain cellulose and / or lignocellulose.
- fluorine-containing compound selected from a fluorine-containing olefin compound, a fluorine-containing acrylate compound, and a fluorine-containing methacrylate compound to obtain cellulose and / or lignocellulose.
- fluorine-containing compound selected from a fluorine-containing olefin compound, a fluorine-containing acrylate compound, and a fluorine-containing methacrylate compound
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU20437/97A AU722728B2 (en) | 1996-03-29 | 1997-03-28 | Process for fluorinating cellulosic materials and fluorinated cellulosic materials |
EP97908532A EP0890579A4 (en) | 1996-03-29 | 1997-03-28 | METHOD FOR FLUORINATING CELLULOSE-CONTAINING MATERIALS AND THE FLUORINATED CELLULOSE-CONTAINING MATERIALS |
US09/155,436 US6293972B1 (en) | 1996-03-29 | 1997-03-28 | Process for fluorinating cellulosic materials and fluorinated cellulosic materials |
BR9708374A BR9708374A (pt) | 1996-03-29 | 1997-03-28 | Método para fluoretação de material celulósico e material celulósico fluoretado |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8/77041 | 1996-03-29 | ||
JP7704196 | 1996-03-29 |
Publications (1)
Publication Number | Publication Date |
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WO1997036934A1 true WO1997036934A1 (fr) | 1997-10-09 |
Family
ID=13622698
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1997/000426 WO1997036933A1 (fr) | 1996-03-29 | 1997-02-18 | Procede de fluoration de materiaux cellulosiques et materiaux cellulosiques fluores |
PCT/JP1997/001061 WO1997036934A1 (fr) | 1996-03-29 | 1997-03-28 | Procede de fluoration de matieres cellulosiques et matieres cellulosiques fluorees |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1997/000426 WO1997036933A1 (fr) | 1996-03-29 | 1997-02-18 | Procede de fluoration de materiaux cellulosiques et materiaux cellulosiques fluores |
Country Status (7)
Country | Link |
---|---|
US (1) | US6293972B1 (ja) |
EP (1) | EP0890579A4 (ja) |
CN (1) | CN1214696A (ja) |
AU (2) | AU1673597A (ja) |
BR (1) | BR9708374A (ja) |
CA (1) | CA2250122A1 (ja) |
WO (2) | WO1997036933A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000024528A1 (en) * | 1998-10-27 | 2000-05-04 | E.I. Du Pont De Nemours And Company | In situ fluoropolymer polymerization into porous substrates |
JP2005531647A (ja) * | 2002-04-11 | 2005-10-20 | カルボマー インク | 新規なイメージングプローブ |
JP2005531648A (ja) * | 2002-04-11 | 2005-10-20 | カルボマー インク | 生体適合性物質およびプローブ類 |
EP1754547A2 (en) * | 1998-10-27 | 2007-02-21 | E. I. du Pont de Nemours and Company | In situ fluoropolymer polymerization into porous substrates |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6306989B1 (en) | 1999-09-30 | 2001-10-23 | E. I. Du Pont De Nemours And Company | Situ fluoropolymer polymerization into porous substrates |
US6558743B1 (en) | 1998-10-27 | 2003-05-06 | E. I. Du Pont De Nemours And Company | In situ fluoropolymer polymerization into porous substrates |
US20030226648A1 (en) * | 2002-06-06 | 2003-12-11 | Mcdonnell William T. | Multiple ply paperboard material having improved oil and grease resistance and stain masking properties and method for forming same |
CA2410213C (en) * | 2002-10-30 | 2011-03-08 | James E. Guillet | Water soluble biodegradable polymeric photocatalysts |
US20070160850A1 (en) * | 2005-12-06 | 2007-07-12 | Osmose, Inc. | Fluoro-compound water repellent composition for wood product dimensional stability |
US8617002B2 (en) * | 2009-06-24 | 2013-12-31 | Acushnet Company | Wedge type golf club head with improved performance |
JP6063135B2 (ja) * | 2012-03-19 | 2017-01-18 | 東洋紡Stc株式会社 | 撥水撥油性を持つ繊維構造物の製造方法 |
CN104294594B (zh) * | 2014-09-19 | 2016-05-18 | 苏州大学 | 一种拒水拒油超疏织物表面的制备方法 |
WO2017144180A1 (de) | 2016-02-25 | 2017-08-31 | Universität Innsbruck | Vernetzbare zusammensetzung und verfahren zur herstellung eines beschichteten artikels |
CN108727506B (zh) * | 2018-06-22 | 2020-08-04 | 四川大学 | 氟化改性纤维素材料及其制备方法 |
CN110804105B (zh) * | 2019-11-05 | 2021-06-04 | 浙江恒川新材料有限公司 | 一种用于食品包装纸的含氟疏水抗油改性纳米纤维素及其制备方法 |
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JPS61171702A (ja) * | 1985-01-24 | 1986-08-02 | Daicel Chem Ind Ltd | 弗素含有セルロ−スエ−テル誘導体 |
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US3489504A (en) * | 1965-02-15 | 1970-01-13 | Koratron Co Inc | Etherification of cellulosic materials and starch with fluorinated monoolefins alone or in conjunction with fluorinated polyolefins |
US3799992A (en) * | 1965-02-18 | 1974-03-26 | Us Agriculture | Fluorinated vinyl ethers and use thereof |
JPS60112829A (ja) | 1983-11-22 | 1985-06-19 | Nippon Mektron Ltd | パ−フルオロエ−テルスルホン酸重合体およびその製造法 |
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JPS625936A (ja) | 1985-06-24 | 1987-01-12 | S D S Baiotetsuku:Kk | フツ素含有芳香族化合物および防菌防黴剤 |
JP2717122B2 (ja) | 1988-11-07 | 1998-02-18 | 株式会社ネオス | 固体潤滑剤 |
JPH02212501A (ja) * | 1989-02-10 | 1990-08-23 | Daikin Ind Ltd | 含フッ素セルロース誘導体 |
JPH02227401A (ja) * | 1989-02-28 | 1990-09-10 | Daikin Ind Ltd | 含フッ素セルロースエステル誘導体 |
US5254774A (en) * | 1992-12-28 | 1993-10-19 | Minnesota Mining And Manufacturing Company | Preparation of hexafluoropropene oligomers |
DE69306578T2 (de) * | 1993-10-19 | 1997-04-10 | Minnesota Mining & Mfg | Hochleistungszusammensetzungen mit wasser- und ölabweisenden Eigenschaften |
-
1997
- 1997-02-18 AU AU16735/97A patent/AU1673597A/en not_active Withdrawn
- 1997-02-18 WO PCT/JP1997/000426 patent/WO1997036933A1/ja active Application Filing
- 1997-03-28 WO PCT/JP1997/001061 patent/WO1997036934A1/ja not_active Application Discontinuation
- 1997-03-28 BR BR9708374A patent/BR9708374A/pt not_active Application Discontinuation
- 1997-03-28 AU AU20437/97A patent/AU722728B2/en not_active Ceased
- 1997-03-28 US US09/155,436 patent/US6293972B1/en not_active Expired - Fee Related
- 1997-03-28 EP EP97908532A patent/EP0890579A4/en not_active Withdrawn
- 1997-03-28 CN CN97193457.6A patent/CN1214696A/zh active Pending
- 1997-03-28 CA CA002250122A patent/CA2250122A1/en not_active Abandoned
Patent Citations (2)
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JPS6186972A (ja) * | 1984-10-05 | 1986-05-02 | Matsushita Electric Works Ltd | 木材の表面処理法 |
JPS61171702A (ja) * | 1985-01-24 | 1986-08-02 | Daicel Chem Ind Ltd | 弗素含有セルロ−スエ−テル誘導体 |
Non-Patent Citations (1)
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See also references of EP0890579A4 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000024528A1 (en) * | 1998-10-27 | 2000-05-04 | E.I. Du Pont De Nemours And Company | In situ fluoropolymer polymerization into porous substrates |
JP2002528569A (ja) * | 1998-10-27 | 2002-09-03 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 多孔質基質に入り込ませた状態のフルオロポリマーのインサイチュー重合 |
EP1754547A2 (en) * | 1998-10-27 | 2007-02-21 | E. I. du Pont de Nemours and Company | In situ fluoropolymer polymerization into porous substrates |
EP1754547A3 (en) * | 1998-10-27 | 2007-05-30 | E. I. du Pont de Nemours and Company | In situ fluoropolymer polymerization into porous substrates |
JP2005531647A (ja) * | 2002-04-11 | 2005-10-20 | カルボマー インク | 新規なイメージングプローブ |
JP2005531648A (ja) * | 2002-04-11 | 2005-10-20 | カルボマー インク | 生体適合性物質およびプローブ類 |
Also Published As
Publication number | Publication date |
---|---|
CN1214696A (zh) | 1999-04-21 |
AU2043797A (en) | 1997-10-22 |
BR9708374A (pt) | 1999-08-03 |
WO1997036933A1 (fr) | 1997-10-09 |
AU1673597A (en) | 1997-10-22 |
CA2250122A1 (en) | 1997-10-09 |
AU722728B2 (en) | 2000-08-10 |
EP0890579A1 (en) | 1999-01-13 |
EP0890579A4 (en) | 2000-03-22 |
US6293972B1 (en) | 2001-09-25 |
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