WO1999062858A1 - Verfahren zur rückgewinnung von fluorierten alkansäuren aus abwässern - Google Patents
Verfahren zur rückgewinnung von fluorierten alkansäuren aus abwässern Download PDFInfo
- Publication number
- WO1999062858A1 WO1999062858A1 PCT/EP1999/003672 EP9903672W WO9962858A1 WO 1999062858 A1 WO1999062858 A1 WO 1999062858A1 EP 9903672 W EP9903672 W EP 9903672W WO 9962858 A1 WO9962858 A1 WO 9962858A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solids
- acids
- waste water
- fluorinated
- acid
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
- C07C53/16—Halogenated acetic acids
- C07C53/18—Halogenated acetic acids containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
- B01J41/04—Processes using organic exchangers
- B01J41/05—Processes using organic exchangers in the strongly basic form
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
- B01J41/20—Anion exchangers for chromatographic processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J49/00—Regeneration or reactivation of ion-exchangers; Apparatus therefor
- B01J49/50—Regeneration or reactivation of ion-exchangers; Apparatus therefor characterised by the regeneration reagents
- B01J49/57—Regeneration or reactivation of ion-exchangers; Apparatus therefor characterised by the regeneration reagents for anionic exchangers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/12—Halogens or halogen-containing compounds
- C02F2101/14—Fluorine or fluorine-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/36—Organic compounds containing halogen
Definitions
- Fluorinated alkanoic acids are used as emulsifiers for the polymerization of fluorinated monomers in aqueous dispersion, since they have no telogenic properties.
- the salts preferably the alkali or ammonium salts, of perfluorinated or partially fluorinated alkane carboxylic acids or sulfonic acids are used. These compounds are produced by electrofluorination or by the telomerization of fluorinated monomers, which is very expensive. There has been no shortage of attempts to recover these valuable materials from wastewater.
- DE-A-20 44 986 discloses a process for obtaining perfluorocarboxylic acids from dilute solution, the dilute solution of the perfluorocarboxylic acids being brought into adsorption contact with a weakly basic anion exchange resin and thereby adsorbing the perfluorocarboxylic acid contained in the solution onto the anion exchange resin, which
- Another aspect of the invention is to be seen in the fact that not only can existing solids be removed, but also other disruptive constituents that can be converted into solids.
- Such disruptive components can other acids or their
- oxalic acid which is often used as a buffer.
- the oxalic acid can be precipitated in whole or in part as a poorly soluble oxalate, advantageously together with any other disruptive, finely divided substances which may be present.
- the invention thus relates to a process for the recovery of fluorinated emulsifier acids from wastewater, which is characterized in that firstly finely divided solids and / or parts which can be converted into solids are removed from the wastewater, then the fluorinated emulsifier acids are bound to an anion exchange resin and from this the fluorinated emulsifier acids eluted. Further aspects of the invention and its preferred embodiments are explained in more detail below.
- Process wastewater which contains surface-active fluorinated alkanoic acids can be considered as wastewater.
- the process is particularly suitable for waste water from the polymerization of fluorinated monomers by the so-called emulsion process, in which the fluorinated monomer is converted into a finely divided polymer, which is present in finely dispersed, colloidal form, with gentle stirring using a relatively high concentration of fluorinated emulsifier acid the latex obtained in this way being coagulated after the desired solids concentration has been reached, for example by vigorous stirring, as a result of which the polymer separates out as a fine powder.
- metal salts for example aluminum salts such as aluminum chloride and aluminum sulfate, calcium salts such as calcium chloride, magnesium salts such as magnesium chloride and magnesium sulfate, iron salts such as iron (II) or iron (III) chloride and iron sulfate.
- aluminum salts such as aluminum chloride and aluminum sulfate
- calcium salts such as calcium chloride
- magnesium salts such as magnesium chloride and magnesium sulfate
- iron salts such as iron (II) or iron (III) chloride and iron sulfate
- iron salts such as iron (II) or iron (III) chloride and iron sulfate.
- acidic waste water it is also possible to add appropriate metals such as aluminum, iron or magnesium. Small amounts of a flocculant can be added to improve the flocculation.
- electrocoagulation Another possibility of precipitating the interfering colloids is electrocoagulation.
- An electric field is applied to the wastewater to coagulate the colloidal particles.
- inert electrodes for example titanium
- the particles are deposited on the surfaces.
- soluble electrodes for example iron and / or aluminum
- metal cations with a large charge and diameter ratio are introduced into the solution, which cause the coagulation as with the addition of metal salts.
- electrocoagulation it is advantageous to avoid the additional introduction of anions, such as chloride or Sulfate. Small amounts of a flocculant can be added to improve the flocculation.
- Cross-flow filtration for example with membranes, centrifuges
- deep-bed filtration for example sand bed filter
- precoat filtration with the addition of a filter aid (for example cellulose, perlite, diatomaceous earth).
- a filter aid for example cellulose, perlite, diatomaceous earth
- the precipitated solids can be separated off in a manner known per se, for example by filtration, if necessary using a filter aid, by decanting, by flotation or sedimentation.
- ® AMBERLITE IRA-402 ® AMBERJET 4200 (both: Rohm & Haas), ® PUROLITE A845 (Purolite GmbH) or ® LEWATIT MP-500 (Bayer AG) are available.
- the adsorption can be carried out in a manner known per se, the exchange resins being arranged in the customary apparatuses, such as tubes or columns, through which the waste water flows.
- the bound emulsifier acids are also eluted in a manner known per se, the process according to US Pat. No. 4,282,162 being preferred.
- the wastewater remaining after the adsorption of the emulsifier acids is worked up in a known manner or returned to the process. If desired, residual portions of fluorinated emulsifier acids can be removed using conventional adsorbents such as activated carbon.
- the PFOS concentration in the liquor is 1200 mg / 1, the oxalic acid concentration 1600 mg / 1.
- the pretreated liquor is conveyed through the column with an upstream pump and at a linear speed of 1 m / h, the escaping water is collected and the
- PFOS concentration determined for accounting. After loading, the column is rinsed with 100 ml of water.
- the eluate contains 85% of the emulsifier acid and oxalic acid contained in the waste water with a concentration of 3900 mg / 1.
- Example 2 In a stirred vessel, 14 l of the liquor are mixed as in Example 1 with 1.5 g / 1 of a 10% by weight aluminum chloride solution and stirred vigorously. A pH of 7.5 is then set with a 10% by weight lime milk solution. The precipitate that forms is filtered off and the pH of the solution is adjusted to pH 4 using dilute sulfuric acid.
- the construction and test sequence of loading and regeneration of the ion exchanger are carried out analogously to Example 1.
- the eluate contains 95% of the emulsifier acid and oxalic acid contained in the waste water with a concentration of 1 mg / 1.
- 16 l of a waste water from the polymer processing of fluorine-containing polymers are placed in a stirred vessel.
- the ammonium salt of the PFOS is used as an emulsifier
- the PFOS concentration is 1200 mg / 1.
- 2 g of a 10% by weight aluminum chloride solution are added to this solution and stirred vigorously. .
- treated with of a 10% strength Kalkmilchweed is adjusted to a pH value of 7.5 and 3 mg / 1 of a flocculating agent (® PRAEST0L A 3015 L, Stockhausen GmbH & Co. KG; polyacrylamide) was added.
- the precipitate that forms is filtered off and the pH is adjusted to pH 4 using sulfuric acid.
- the ion exchanger is loaded and regenerated as in Example 1.
- the eluate contains 91% of the emulsifier acid contained in the waste water.
- the PFOS concentration is 1200 mg / 1.
- Example 1 About 50 ml of the strongly basic ion exchange resin mentioned in Example 1 are placed in a cylindrical glass column provided with a glass frit (length 25 cm, diameter 16 mm) and rinsed with water. In order to load the ion exchanger, the liquor is conveyed untreated through the bed with a pump. The pressure loss across the ion exchanger bed is measured with a manometer. The loading test had to be stopped after transferring 400 ml of the liquor, since the resin stuck due to polymer failure.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Environmental & Geological Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Treatment Of Water By Ion Exchange (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Removal Of Specific Substances (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
Description
Claims
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/700,636 US6613941B1 (en) | 1998-06-02 | 1999-05-27 | Method for recovering fluorinated alkanoic acids from waste waters |
| AU43701/99A AU4370199A (en) | 1998-06-02 | 1999-05-27 | Method for recovering fluorinated alkanoic acids from waste waters |
| AT99926442T ATE222229T1 (de) | 1998-06-02 | 1999-05-27 | Verfahren zur rückgewinnung von fluorierten alkansäuren aus abwässern |
| JP2000552073A JP3678651B2 (ja) | 1998-06-02 | 1999-05-27 | 廃水からの弗素化アルカン酸の回収方法 |
| PL344576A PL193358B1 (pl) | 1998-06-02 | 1999-05-27 | Sposób regeneracji fluorowanych kwasów emulgatora ze ścieków |
| HU0102469A HUP0102469A2 (hu) | 1998-06-02 | 1999-05-27 | Eljárás fluorozott alkánsavak visszanyerésére szennyvizekből |
| DE59902354T DE59902354D1 (de) | 1998-06-02 | 1999-05-27 | Verfahren zur rückgewinnung von fluorierten alkansäuren aus abwässern |
| EP99926442A EP1084097B1 (de) | 1998-06-02 | 1999-05-27 | Verfahren zur rückgewinnung von fluorierten alkansäuren aus abwässern |
| CA002334105A CA2334105A1 (en) | 1998-06-02 | 1999-05-27 | Process for the recovery of fluorinated alkanoic acids from wastewater |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19824614.5 | 1998-06-02 | ||
| DE19824614A DE19824614A1 (de) | 1998-06-02 | 1998-06-02 | Verfahren zur Rückgewinnung von fluorierten Alkansäuren aus Abwässern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1999062858A1 true WO1999062858A1 (de) | 1999-12-09 |
Family
ID=7869667
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP1999/003672 Ceased WO1999062858A1 (de) | 1998-06-02 | 1999-05-27 | Verfahren zur rückgewinnung von fluorierten alkansäuren aus abwässern |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6613941B1 (de) |
| EP (2) | EP1084097B1 (de) |
| JP (1) | JP3678651B2 (de) |
| KR (1) | KR100518480B1 (de) |
| CN (1) | CN1134403C (de) |
| AT (2) | ATE307793T1 (de) |
| AU (1) | AU4370199A (de) |
| CA (1) | CA2334105A1 (de) |
| DE (3) | DE19824614A1 (de) |
| ES (1) | ES2176137T3 (de) |
| HU (1) | HUP0102469A2 (de) |
| PL (1) | PL193358B1 (de) |
| RU (1) | RU2226186C2 (de) |
| TR (1) | TR200003530T2 (de) |
| WO (1) | WO1999062858A1 (de) |
| ZA (1) | ZA200006907B (de) |
Cited By (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001005710A1 (de) * | 1999-07-17 | 2001-01-25 | Dyneon Gmbh & Co. Kg | Verfahren zur rückgewinnung fluorierter emulgatoren aus wässrigen phasen |
| US6281374B1 (en) * | 2000-08-23 | 2001-08-28 | E. I. Du Pont De Nemours And Company | Fluorinated alkanoic acid purification process |
| US6436244B1 (en) | 1999-07-14 | 2002-08-20 | Dyneon Gmbh | Process for the elution of fluorinated emulsifiers |
| EP1314700A1 (de) * | 2001-11-22 | 2003-05-28 | Asahi Glass Company Ltd. | Verfahren zur Absorption und zur Rückgewinnung von fluorenthaltenden Emulgatoren |
| US6642415B1 (en) | 1999-11-05 | 2003-11-04 | 3M Innovative Properties Company | Method for recovering fluorinated emulsifiers |
| US6737489B2 (en) | 2001-05-21 | 2004-05-18 | 3M Innovative Properties Company | Polymers containing perfluorovinyl ethers and applications for such polymers |
| US6794550B2 (en) | 2000-04-14 | 2004-09-21 | 3M Innovative Properties Company | Method of making an aqueous dispersion of fluoropolymers |
| US6822059B2 (en) | 2002-04-05 | 2004-11-23 | 3M Innovative Properties Company | Dispersions containing bicomponent fluoropolymer particles and use thereof |
| US6833418B2 (en) | 2002-04-05 | 2004-12-21 | 3M Innovative Properties Company | Dispersions containing perfluorovinyl ether homopolymers and use thereof |
| EP1561742A1 (de) * | 2004-02-05 | 2005-08-10 | 3M Innovative Properties Company | Verfahren zur Rückgewinnung von fluorierten, Säuregruppen enthaltenden Tensiden von damit beladenen Adsorptionsmitteln |
| US7045571B2 (en) | 2001-05-21 | 2006-05-16 | 3M Innovative Properties Company | Emulsion polymerization of fluorinated monomers |
| EP1700869A1 (de) | 2005-03-11 | 2006-09-13 | 3M Innovative Properties Company | Rückgewinnung fluorierter Tenside aus basischen Anionenaustauscherharzen enthaltend quartäre Ammoniumgruppen |
| US8404790B2 (en) | 2005-07-15 | 2013-03-26 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for producing fluoropolymers |
| US9212693B2 (en) | 2007-04-27 | 2015-12-15 | 3M Innovative Properties Company | Fluoropolymer coated articles |
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|---|---|---|---|---|
| DE19824615A1 (de) * | 1998-06-02 | 1999-12-09 | Dyneon Gmbh | Verfahren zur Rückgewinnung von fluorierten Alkansäuren aus Abwässern |
| DE19857111A1 (de) * | 1998-12-11 | 2000-06-15 | Dyneon Gmbh | Wäßrige Dispersionen von Fluorpolymeren |
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- 1999-05-27 KR KR10-2000-7013634A patent/KR100518480B1/ko not_active Expired - Fee Related
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- 1999-05-27 HU HU0102469A patent/HUP0102469A2/hu unknown
- 1999-05-27 TR TR2000/03530T patent/TR200003530T2/xx unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6436244B1 (en) | 1999-07-14 | 2002-08-20 | Dyneon Gmbh | Process for the elution of fluorinated emulsifiers |
| WO2001005710A1 (de) * | 1999-07-17 | 2001-01-25 | Dyneon Gmbh & Co. Kg | Verfahren zur rückgewinnung fluorierter emulgatoren aus wässrigen phasen |
| US6706193B1 (en) | 1999-07-17 | 2004-03-16 | 3M Innovative Properties Company | Method for recovering fluorinated emulsifiers from aqueous phases |
| US6642415B1 (en) | 1999-11-05 | 2003-11-04 | 3M Innovative Properties Company | Method for recovering fluorinated emulsifiers |
| US6794550B2 (en) | 2000-04-14 | 2004-09-21 | 3M Innovative Properties Company | Method of making an aqueous dispersion of fluoropolymers |
| US6281374B1 (en) * | 2000-08-23 | 2001-08-28 | E. I. Du Pont De Nemours And Company | Fluorinated alkanoic acid purification process |
| US7045571B2 (en) | 2001-05-21 | 2006-05-16 | 3M Innovative Properties Company | Emulsion polymerization of fluorinated monomers |
| US6737489B2 (en) | 2001-05-21 | 2004-05-18 | 3M Innovative Properties Company | Polymers containing perfluorovinyl ethers and applications for such polymers |
| US7262246B2 (en) | 2001-05-21 | 2007-08-28 | 3M Innovative Properties Company | Emulsion polymerization of fluorinated monomers |
| EP1314700A1 (de) * | 2001-11-22 | 2003-05-28 | Asahi Glass Company Ltd. | Verfahren zur Absorption und zur Rückgewinnung von fluorenthaltenden Emulgatoren |
| US6822059B2 (en) | 2002-04-05 | 2004-11-23 | 3M Innovative Properties Company | Dispersions containing bicomponent fluoropolymer particles and use thereof |
| US6833418B2 (en) | 2002-04-05 | 2004-12-21 | 3M Innovative Properties Company | Dispersions containing perfluorovinyl ether homopolymers and use thereof |
| US7199196B2 (en) | 2002-04-05 | 2007-04-03 | 3M Innovative Properties Company | Dispersions containing perfluorovinyl ether homopolymers and use thereof |
| US7300989B2 (en) | 2002-04-05 | 2007-11-27 | 3M Innovative Properties Company | Dispersions containing bicomponent fluoropolymer particles and use thereof |
| EP1561742A1 (de) * | 2004-02-05 | 2005-08-10 | 3M Innovative Properties Company | Verfahren zur Rückgewinnung von fluorierten, Säuregruppen enthaltenden Tensiden von damit beladenen Adsorptionsmitteln |
| WO2005077880A1 (en) * | 2004-02-05 | 2005-08-25 | 3M Innovative Properties Company | Method of recovering fluorinated acid surfactants from adsorbent particles loaded therewith |
| EP1700869A1 (de) | 2005-03-11 | 2006-09-13 | 3M Innovative Properties Company | Rückgewinnung fluorierter Tenside aus basischen Anionenaustauscherharzen enthaltend quartäre Ammoniumgruppen |
| US8404790B2 (en) | 2005-07-15 | 2013-03-26 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for producing fluoropolymers |
| US9212693B2 (en) | 2007-04-27 | 2015-12-15 | 3M Innovative Properties Company | Fluoropolymer coated articles |
| WO2019156175A1 (ja) | 2018-02-08 | 2019-08-15 | ダイキン工業株式会社 | フルオロポリマーの製造方法、重合用界面活性剤、界面活性剤の使用及び組成物 |
| WO2019168183A1 (ja) | 2018-03-01 | 2019-09-06 | ダイキン工業株式会社 | フルオロポリマーの製造方法 |
| EP4317214A2 (de) | 2018-03-01 | 2024-02-07 | Daikin Industries, Ltd. | Verfahren zur herstellung von fluorpolymer |
| WO2019172382A1 (ja) | 2018-03-07 | 2019-09-12 | ダイキン工業株式会社 | フルオロポリマーの製造方法 |
| WO2020158940A1 (ja) | 2019-02-01 | 2020-08-06 | ダイキン工業株式会社 | ポリテトラフルオロエチレンの製造方法 |
| WO2020162623A1 (ja) | 2019-02-07 | 2020-08-13 | ダイキン工業株式会社 | 組成物、延伸体及びその製造方法 |
| WO2020213691A1 (ja) | 2019-04-16 | 2020-10-22 | ダイキン工業株式会社 | フルオロポリマー粉末の製造方法 |
| WO2021015291A1 (ja) | 2019-07-23 | 2021-01-28 | ダイキン工業株式会社 | フルオロポリマーの製造方法、ポリテトラフルオロエチレン組成物及びポリテトラフルオロエチレン粉末 |
| WO2021045228A1 (ja) | 2019-09-05 | 2021-03-11 | ダイキン工業株式会社 | ポリテトラフルオロエチレン水性分散液 |
| WO2021045227A1 (ja) | 2019-09-05 | 2021-03-11 | ダイキン工業株式会社 | 組成物およびその製造方法 |
| EP4685166A2 (de) | 2019-09-05 | 2026-01-28 | Daikin Industries, Ltd. | Zusammensetzung und verfahren zu ihrer herstellung |
| EP4707314A2 (de) | 2019-09-05 | 2026-03-11 | Daikin Industries, Ltd. | Zusammensetzung und verfahren zu ihrer herstellung |
| WO2021066189A1 (ja) | 2019-10-03 | 2021-04-08 | ダイキン工業株式会社 | ポリテトラフルオロエチレンおよびその製造方法 |
| WO2021100834A1 (ja) | 2019-11-19 | 2021-05-27 | ダイキン工業株式会社 | ポリテトラフルオロエチレンの製造方法 |
| WO2022050430A1 (ja) | 2020-09-07 | 2022-03-10 | ダイキン工業株式会社 | 変性ポリテトラフルオロエチレン水性分散液 |
| US12410071B1 (en) | 2020-10-19 | 2025-09-09 | Wm Intellectual Property Holdings, L.L.C. | System and method for removal of PFAS and other emerging contaminant micro-constituents from landfill leachate and other impacted liquids |
| WO2022107894A1 (ja) | 2020-11-19 | 2022-05-27 | ダイキン工業株式会社 | ポリテトラフルオロエチレンの製造方法およびポリテトラフルオロエチレンを含有する組成物 |
| WO2023208919A1 (en) | 2022-04-28 | 2023-11-02 | Röhm Gmbh | Poly(meth)acrylat impact modifier with reduced metal ion content and method for its production |
Also Published As
| Publication number | Publication date |
|---|---|
| PL344576A1 (en) | 2001-11-05 |
| ATE307793T1 (de) | 2005-11-15 |
| HUP0102469A2 (hu) | 2001-10-28 |
| AU4370199A (en) | 1999-12-20 |
| CN1303363A (zh) | 2001-07-11 |
| ZA200006907B (en) | 2001-08-07 |
| EP1084097B1 (de) | 2002-08-14 |
| CN1134403C (zh) | 2001-07-11 |
| ES2176137T3 (es) | 2003-03-01 |
| EP1193242A1 (de) | 2002-04-03 |
| ATE222229T1 (de) | 2002-08-15 |
| TR200003530T2 (tr) | 2001-03-21 |
| US6613941B1 (en) | 2003-09-02 |
| JP3678651B2 (ja) | 2005-08-03 |
| DE59912723D1 (de) | 2005-12-01 |
| DE19824614A1 (de) | 1999-12-09 |
| RU2226186C2 (ru) | 2004-03-27 |
| ES2176137T1 (es) | 2002-12-01 |
| KR20010071377A (ko) | 2001-07-28 |
| DE59902354D1 (de) | 2002-09-19 |
| KR100518480B1 (ko) | 2005-10-05 |
| PL193358B1 (pl) | 2007-02-28 |
| EP1193242B1 (de) | 2005-10-26 |
| CA2334105A1 (en) | 1999-12-09 |
| EP1084097A1 (de) | 2001-03-21 |
| JP2002516892A (ja) | 2002-06-11 |
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