EP1208065A1 - Method for recovering fluorinated emulsifiers from aqueous phases - Google Patents
Method for recovering fluorinated emulsifiers from aqueous phasesInfo
- Publication number
- EP1208065A1 EP1208065A1 EP00954467A EP00954467A EP1208065A1 EP 1208065 A1 EP1208065 A1 EP 1208065A1 EP 00954467 A EP00954467 A EP 00954467A EP 00954467 A EP00954467 A EP 00954467A EP 1208065 A1 EP1208065 A1 EP 1208065A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aqueous phase
- emulsifier
- concentration
- exchange resin
- nonionic surfactant
- 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
- 238000000034 method Methods 0.000 title claims abstract description 32
- 239000003995 emulsifying agent Substances 0.000 title claims abstract description 29
- 239000008346 aqueous phase Substances 0.000 title claims abstract description 19
- 239000002245 particle Substances 0.000 claims abstract description 24
- 239000004811 fluoropolymer Substances 0.000 claims abstract description 14
- 229920002313 fluoropolymer Polymers 0.000 claims abstract description 13
- 239000004094 surface-active agent Substances 0.000 claims abstract description 12
- 239000011347 resin Substances 0.000 claims abstract description 11
- 229920005989 resin Polymers 0.000 claims abstract description 11
- 239000002736 nonionic surfactant Substances 0.000 claims description 11
- 239000003957 anion exchange resin Substances 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 8
- 238000005345 coagulation Methods 0.000 claims description 6
- 230000015271 coagulation Effects 0.000 claims description 6
- 238000011084 recovery Methods 0.000 claims description 6
- 150000001450 anions Chemical group 0.000 claims description 5
- 238000001179 sorption measurement Methods 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 238000003795 desorption Methods 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 125000000373 fatty alcohol group Chemical group 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 239000010419 fine particle Substances 0.000 abstract 1
- 239000002351 wastewater Substances 0.000 description 32
- 239000004816 latex Substances 0.000 description 13
- 229920000126 latex Polymers 0.000 description 13
- 238000006116 polymerization reaction Methods 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 7
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- ABDBNWQRPYOPDF-UHFFFAOYSA-N carbonofluoridic acid Chemical class OC(F)=O ABDBNWQRPYOPDF-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- -1 alkane carboxylic acids Chemical class 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 239000008394 flocculating agent Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- FOKCKXCUQFKNLD-UHFFFAOYSA-N pent-1-enyl hypofluorite Chemical compound C(CC)C=COF FOKCKXCUQFKNLD-UHFFFAOYSA-N 0.000 description 2
- YFSUTJLHUFNCNZ-UHFFFAOYSA-N perfluorooctane-1-sulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YFSUTJLHUFNCNZ-UHFFFAOYSA-N 0.000 description 2
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229960004670 didecyldimethylammonium chloride Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- ONJQDTZCDSESIW-UHFFFAOYSA-N polidocanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO ONJQDTZCDSESIW-UHFFFAOYSA-N 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- 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
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
- C02F1/547—Tensides
-
- 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
-
- 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
-
- 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
Definitions
- the invention relates to the treatment of waste water, especially weakly contaminated waste water, which contain fluorinated emulsifiers, such as are used in the polymerization of fluorinated monomers, 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 waste water.
- a process for the recovery of fluorinated carboxylic acids in usable form from contaminated starting materials is known from US Pat. No. 5,442,097, where necessary the fluorinated carboxylic acid is released from these materials in an aqueous medium with a sufficiently strong acid, and these are reacted with a suitable alcohol and distilled off the ester formed.
- a polymerization liquor can be used as the starting material, in particular from so-called emulsion polymerization, in which the fluoropolymer is produced in the form of colloidal particles with the aid of relatively high amounts of emulsifier.
- Polymerization liquor is the wastewater that is obtained when the fluoropolymer is isolated by coagulation (without further process steps such as washing). This The process has proven itself very well, but requires a certain concentration of fluorinated carboxylic acid in the starting material.
- Carboxylic acids can also be carried out in the absence of alcohols.
- the fluorocarboxylic acid is distilled off in the form of a highly concentrated azeotrope.
- this method variant is not technically advantageous for energy reasons.
- the resulting wastewater is also more polluted than before treatment.
- 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 based anion exchange resin and thereby the perfluorocarboxylic acid contained in the solution to the anions - Exchange resin adsorbed, the anion exchange resin eluted with an aqueous ammonia solution and thus the adsorbed perfluorocarboxylic acid is converted into the eluent and finally the acid from the eluate is recovered.
- relatively large amounts of dilute ammonia solution are required for complete elution and, moreover, this process is very time consuming.
- fluorinated emulsifier acids which is characterized in that the solids finely divided in the waste water are stabilized with a surfactant or a surface-active substance and then the fluorinated emulsifier acids are bound to an anion exchange resin and the fluorinated emulsifier acids are eluted from this (WO -A-99/62830).
- nonionic surfactants are used in a concentration of 100 to 400 mg / 1.
- a process has now been found for recovering fluorinated emulsifiers from an aqueous phase, this aqueous phase containing small amounts of fluoropolymer particles and optionally further substances in addition to the emulsifier, an upper concentration value of a nonionic surface-active substance being determined, below which no further decrease in the Desorption of the emulsifier bound to an anion exchanger occurs, - the aqueous phase is adjusted to a concentration of nonionic surfactant between the upper concentration value determined in this way or a lower concentration which is still effective to avoid coagulation of the polymer particles, brings the aqueous phase thus adjusted into contact with an anionic exchange resin in order to effect adsorption of the emulsifier on the exchange resin and to release the emulsifier from the exchange resin.
- the suitable concentration of nonionic surface-active agent depends on the type of polymer, on the surface-active agent and optionally on other substances contained in the aqueous phase. It is therefore advisable to determine the appropriate concentration limits on the nonionic surfactant for each wastewater to be treated. Usually a concentration of at most 10 ppm is sufficient, mostly a concentration in the range of 5 to 0.1 ppm.
- fluoropolymers such as polytetrafluoroethylene, fluorothermoplastics and fluoroelastomers
- the polymers are separated by coagulation, these being mechanically subject to high shear ratios or chemically by means of coagulation
- the coagulated fluoropolymers are usually agglomerated and washed with water. This results in relatively high amounts of process waste water, namely usually about 5 to 10 t of waste water per 1 t
- Fluoropolymer Fluoropolymer.
- the fluorinated emulsifier is largely washed out and is thus found in the waste water.
- the concentration is usually a few millimoles per liter, corresponding to about 1000 ppm.
- the wastewater also contains chemicals from the polymerization, such as initiators and buffers, which are approximately of the same order of magnitude as the emulsifier, and very small amounts of fluoropolymer latex particles which have not been coagulated.
- the proportion of these latex particles in the wastewater is usually less than 0.5% by weight.
- Another advantage of the low concentrations of nonionic surfactant is the more effective separation of the latex particles from the anion-exchanged wastewater. These particles are advantageously coagulated with small amounts of organic flocculant, it being found that the amount of flocculant required increases with increasing concentration of nonionic surface-active agent.
- the fluoropolymers obtained in this way, now loaded with small amounts of surface-active agent and flocculant, can be used in building materials and therefore do not have to be worked up or deposited in a complex manner.
- oxethylates and oxpropylates of organic hydroxy compounds are suitable as nonionic surface-active agents, non-aromatic oxalkylates being preferred for reasons of environmental protection. Oxethylates of long-chain alcohols are therefore preferably used.
- the organic flocculants are advantageously cationic products, for example polydiallyldimethylammonium chloride.
- Cationic surfactants such as didecyldimethylammonium chloride can also be used to precipitate the nonionic stabilized latex particles.
- their use on an industrial scale is problematic because, when the precipitation is carried out improperly, the particles are reloaded into cationically stabilized latex particles. This significantly reduces the degree of felling.
- the invention is explained in more detail in the following examples.
- wastewater from mechanically coagulated polymer dispersions which contained approximately 90% by weight of the perfluorooctanoic acid used in the polymerization and latex particles. They are not diluted with washing water from the agglomerated resins.
- the dimensions of the anion exchange column were: height 5 cm, diameter 4 cm, filling quantity 500 ml, flow rate 0.5 to 1 l / h, procedure: from top to bottom.
- a commercially available, strongly basic ion exchanger ® AMPERLITE IRA 402 was used, capacity: 1.2 mmol / ml.
- Polymerization liquor from the polymerization of the terpolymer from tetrafluoroethylene, hexafluoropropene and vinylidene fluoride with 0.3% by weight polymer-latex particles and 0.1% by weight perfluorooctanoic acid.
- a commercial p-octylphenol oxyethylate ® TRITON X 100 was used
- Example 1 is repeated with the modification that a commercially available fatty alcohol polyglycol ether ® GENAPOL X 080 (Hoechst AG) was used as the nonionic surface-active agent.
- Example 2 was repeated, but using a process wastewater ("polymerization liquor") from the polymerization of a copolymer of tetrafluoroethylene with perfluoro (n-propyl-vinyl) ether containing 0.1% by weight of perfluorooctanoic acid and 0.4% by weight. % Polymer latex particles was used.
- Example 2 was repeated, but using a process wastewater ("polymerization liquor”) from the polymerization of a copolymer of tetrafluoroethylene with ethylene with 0.2% by weight of perfluorooctanoic acid and 0.6% by weight of polymer latex particles.
- polymerization liquor a process wastewater from the polymerization of a copolymer of tetrafluoroethylene with ethylene with 0.2% by weight of perfluorooctanoic acid and 0.6% by weight of polymer latex particles.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Removal Of Specific Substances (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
- Treatment Of Water By Ion Exchange (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19933696A DE19933696A1 (en) | 1999-07-17 | 1999-07-17 | Process for the recovery of fluorinated emulsifiers from aqueous phases |
DE19933696 | 1999-07-17 | ||
PCT/EP2000/006556 WO2001005710A1 (en) | 1999-07-17 | 2000-07-11 | Method for recovering fluorinated emulsifiers from aqueous phases |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1208065A1 true EP1208065A1 (en) | 2002-05-29 |
Family
ID=7915221
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00954467A Ceased EP1208065A1 (en) | 1999-07-17 | 2000-07-11 | Method for recovering fluorinated emulsifiers from aqueous phases |
Country Status (21)
Country | Link |
---|---|
US (1) | US6706193B1 (en) |
EP (1) | EP1208065A1 (en) |
JP (1) | JP3820369B2 (en) |
KR (1) | KR100447479B1 (en) |
CN (1) | CN1145587C (en) |
AR (1) | AR024730A1 (en) |
AU (1) | AU767303B2 (en) |
BR (1) | BR0012520A (en) |
CA (1) | CA2379931A1 (en) |
CZ (1) | CZ2002128A3 (en) |
DE (1) | DE19933696A1 (en) |
ES (1) | ES2173825T1 (en) |
HU (1) | HUP0201949A3 (en) |
MX (1) | MXPA02000597A (en) |
PL (1) | PL364027A1 (en) |
RU (1) | RU2248328C2 (en) |
SA (1) | SA00210609B1 (en) |
TR (1) | TR200200135T2 (en) |
TW (1) | TW574151B (en) |
WO (1) | WO2001005710A1 (en) |
ZA (1) | ZA200200397B (en) |
Families Citing this family (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19857111A1 (en) * | 1998-12-11 | 2000-06-15 | Dyneon Gmbh | Aqueous dispersions of fluoropolymers |
US6794457B2 (en) | 2001-04-30 | 2004-09-21 | 3M Innovative Properties Company | Fluoropolymer curing system containing a nitrogen cure site monomer |
US7279522B2 (en) * | 2001-09-05 | 2007-10-09 | 3M Innovative Properties Company | Fluoropolymer dispersions containing no or little low molecular weight fluorinated surfactant |
JP2003094052A (en) * | 2001-09-21 | 2003-04-02 | Asahi Glass Co Ltd | Method for adsorbing and recovering emulsifier containing fluorine |
WO2004050719A1 (en) * | 2002-11-29 | 2004-06-17 | Daikin Industries, Ltd. | Method for purification of aqueous fluoropolymer emulsions, purified emulsions, and fluorine-containing finished articles |
EP1441014A1 (en) * | 2003-01-22 | 2004-07-28 | 3M Innovative Properties Company | Aqueous fluoropolymer dispersion comprising a melt processible fluoropolymer and having a reduced amount of fluorinated surfactant |
US6991732B2 (en) | 2003-07-02 | 2006-01-31 | Arkema | Process for the recovery of fluorosurfactants by active charcoal |
FR2856934B1 (en) * | 2003-07-02 | 2005-08-19 | Atofina | PROCESS FOR RECOVERING FLUORINATED SURFACTANTS WITH ACTIVE COAL |
EP1529785B1 (en) * | 2003-10-24 | 2011-03-16 | 3M Innovative Properties Company | Aqueous dispersions of polytetrafluoroethylene particles |
EP1533325B1 (en) * | 2003-11-17 | 2011-10-19 | 3M Innovative Properties Company | Aqueous dispersions of polytetrafluoroethylene having a low amount of fluorinated surfactant |
WO2005066218A1 (en) * | 2003-12-30 | 2005-07-21 | 3M Innovative Properties Company | Fluoropolymer coagulation method and composition |
ATE433350T1 (en) * | 2004-03-01 | 2009-06-15 | 3M Innovative Properties Co | METHOD FOR COATING AN OBJECT WITH A PLASTIC DISPERSION CONTAINING FLUORINE |
US20060014887A1 (en) * | 2004-07-19 | 2006-01-19 | 3M Innovative Properties Company | Method of hydrolyzing a dispersion of ionic fluoropolymer |
US7304101B2 (en) * | 2004-07-19 | 2007-12-04 | 3M Innovative Properties Company | Method of purifying a dispersion of ionic fluoropolymer |
EP1799722B1 (en) * | 2004-08-11 | 2008-12-17 | E.I. Du Pont De Nemours And Company | Removing fluorosurfactant from aqueous fluoropolymer dispersion using sorbent pouches |
US7790041B2 (en) * | 2004-08-11 | 2010-09-07 | E.I. Du Pont De Nemours And Company | Removing fluorosurfactant from aqueous fluoropolymer dispersions |
US20070023360A1 (en) * | 2005-08-01 | 2007-02-01 | Noelke Charles J | Removing fluorosurfactant from aqueous fluoropolymer dispersion using sorbent pouches |
US7402630B2 (en) | 2004-12-16 | 2008-07-22 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
US7619018B2 (en) * | 2004-12-22 | 2009-11-17 | E.I. Du Pont De Nemours And Company | Process for removing fluorosurfactant from aqueous fluoropolymer dispersions and reducing scum formation |
US20060135681A1 (en) * | 2004-12-22 | 2006-06-22 | Cavanaugh Robert J | Viscosity control for reduced fluorosurfactant aqueous fluoropolymer dispersions by the addition of cationic surfactant |
US20060178472A1 (en) * | 2005-02-10 | 2006-08-10 | Johnson David W | Process for producing low fluorosurfactant-containing aqueous fluoropolymer dispersions with controlled pH |
US7671111B2 (en) * | 2005-02-10 | 2010-03-02 | E.I. Du Pont De Nemours And Company | Monitoring column breakthrough in a process for removing fluorosurfactant from aqueous fluoropolymer dispersions |
GB2427170A (en) * | 2005-06-17 | 2006-12-20 | 3M Innovative Properties Co | Fluoropolymer film having glass microspheres |
JP4977970B2 (en) * | 2005-06-22 | 2012-07-18 | ダイキン工業株式会社 | Method for producing nonionic surfactant aqueous composition |
GB0514398D0 (en) | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a fluorinated surfactant |
GB0525978D0 (en) * | 2005-12-21 | 2006-02-01 | 3M Innovative Properties Co | Fluorinated Surfactants For Making Fluoropolymers |
GB0514387D0 (en) * | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a perfluoropolyether surfactant |
GB0523853D0 (en) | 2005-11-24 | 2006-01-04 | 3M Innovative Properties Co | Fluorinated surfactants for use in making a fluoropolymer |
US7671112B2 (en) | 2005-07-15 | 2010-03-02 | 3M Innovative Properties Company | Method of making fluoropolymer dispersion |
US20080015304A1 (en) | 2006-07-13 | 2008-01-17 | Klaus Hintzer | Aqueous emulsion polymerization process for producing fluoropolymers |
US7294677B2 (en) | 2005-08-25 | 2007-11-13 | 3M Innovative Properties Company | Catalyst for making fluoroelastomer compositions and methods of using the same |
GB2430437A (en) * | 2005-09-27 | 2007-03-28 | 3M Innovative Properties Co | Method of making a fluoropolymer |
RU2388537C2 (en) * | 2005-10-14 | 2010-05-10 | Асахи Гласс Компани, Лимитед | Method of regenerating basic ion exchange resin |
US7728087B2 (en) | 2005-12-23 | 2010-06-01 | 3M Innovative Properties Company | Fluoropolymer dispersion and method for making the same |
US7754795B2 (en) | 2006-05-25 | 2010-07-13 | 3M Innovative Properties Company | Coating composition |
US20070276103A1 (en) * | 2006-05-25 | 2007-11-29 | 3M Innovative Properties Company | Fluorinated Surfactants |
US8119750B2 (en) | 2006-07-13 | 2012-02-21 | 3M Innovative Properties Company | Explosion taming surfactants for the production of perfluoropolymers |
BRPI0807109A2 (en) * | 2007-02-16 | 2014-05-06 | 3M Innovative Properties Co | Water Fluorochemical Removal System and Process |
WO2008109219A1 (en) * | 2007-03-06 | 2008-09-12 | 3M Innovative Properties Company | System and process for ultrasonically induced cavitation of fluorochemicals |
US20080264864A1 (en) * | 2007-04-27 | 2008-10-30 | 3M Innovative Properties Company | PROCESS FOR REMOVING FLUORINATED EMULSIFIER FROM FLUOROPOLMER DISPERSIONS USING AN ANION-EXCHANGE RESIN AND A pH-DEPENDENT SURFACTANT AND FLUOROPOLYMER DISPERSIONS CONTAINING A pH-DEPENDENT SURFACTANT |
GB0712191D0 (en) † | 2007-06-25 | 2007-08-01 | 3M Innovative Properties Co | Process for removing fluorinated compounds for an aqueous phase originating from the preparation of fluoropolymers |
JP5584123B2 (en) * | 2007-09-14 | 2014-09-03 | スリーエム イノベイティブ プロパティズ カンパニー | Ultra low viscosity iodine-containing amorphous fluoropolymer |
JP5452508B2 (en) * | 2008-02-29 | 2014-03-26 | スリーエム イノベイティブ プロパティズ カンパニー | Perfluoroelastomers with low carbonyl end groups |
KR101684719B1 (en) | 2009-06-25 | 2016-12-08 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | Curing compositions for fluoropolymers |
US20130168319A1 (en) * | 2010-02-18 | 2013-07-04 | Lanxess Deutschland Gmbh | Treatment of waste water containing fluorinated acids or the salts thereof |
CN103717624B (en) * | 2011-07-28 | 2016-10-19 | 阿科玛股份有限公司 | Use the method that alkyl sulfate surfactant produces fluoropolymer |
EP2557109B1 (en) | 2011-08-11 | 2019-01-23 | 3M Innovative Properties Company | Method of bonding a fluoroelastomer compound to a metal substrate using low molecular weight functional hydrocarbons as bonding promoter |
US20150299356A1 (en) | 2012-11-05 | 2015-10-22 | 3M Innovative Properties Company | Peroxide-curable fluoropolymer composition including solvent and method of using the same |
EP2935443B1 (en) | 2012-12-20 | 2017-02-01 | 3M Innovative Properties Company | Composite particles including a fluoropolymer, methods of making, and articles including the same |
CN103395860B (en) * | 2013-08-07 | 2014-12-31 | 邱峰 | Method and device for clarifying fluorine-containing wastewater |
CA2924818A1 (en) | 2013-09-20 | 2015-03-26 | 3M Innovative Properties Company | Polymer processing additive, compositions, and methods |
EP3056275B1 (en) * | 2013-10-10 | 2020-04-29 | AGC Inc. | Method for recovering fluorinated emulsifier |
CN104529031B (en) * | 2014-12-08 | 2016-05-04 | 北京师范大学 | From sewage, reclaim the method for perfluorochemical |
CN107108983B (en) | 2014-12-19 | 2020-11-03 | 3M创新有限公司 | Poly (oxyalkylene) polymer processing additives, compositions and methods |
WO2016130911A1 (en) | 2015-02-12 | 2016-08-18 | 3M Innovative Properties Company | Tetrafluoroethylene/hexafluoropropylene copolymers including perfluoroalkoxyalkyl pendant groups and methods of making and using the same |
US10730980B2 (en) | 2015-02-12 | 2020-08-04 | 3M Innovative Properties Company | Tetrafluoroethylene/hexafluoropropylene copolymers including perfluoroalkoxyalkyl pendant groups |
EP3256499B1 (en) | 2015-02-12 | 2018-12-05 | 3M Innovative Properties Company | Tetrafluoroethylene copolymers having sulfonyl groups |
CN108137750A (en) | 2015-09-23 | 2018-06-08 | 3M创新有限公司 | The method for preparing the TFE copolymer with sulfonyl side group |
CN108137880A (en) | 2015-10-13 | 2018-06-08 | 3M创新有限公司 | Fluoropolymer processing additives, composition and method |
US20200255646A1 (en) | 2015-11-13 | 2020-08-13 | 3M Innovative Properties Company | Compositions including amorphous fluoropolymers and methods of using the same |
KR20180104305A (en) | 2016-01-21 | 2018-09-20 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | Lamination of Fluoropolymers |
TW201815845A (en) | 2016-05-17 | 2018-05-01 | 3M新設資產公司 | Compositions including copolymers of vinylidene fluoride and tetrafluoroethylene and methods of using the same |
CN109563206A (en) | 2016-08-17 | 2019-04-02 | 3M创新有限公司 | Tetrafluoroethene and perfluorinated allyl ethers copolymer |
US20190344496A1 (en) | 2016-12-20 | 2019-11-14 | 3M Innovative Properties Company | Composition including fluoropolymer and inorganic filler and method of making a three-dimensional article |
CN110770200B (en) | 2017-05-19 | 2022-10-04 | 3M创新有限公司 | Process for preparing polyfluorinated allyl ethers and compounds related thereto |
EP3681949A4 (en) | 2017-09-14 | 2021-07-14 | 3M Innovative Properties Company | Fluorinated copolymer and compositions and articles including the same |
CN111278578A (en) * | 2017-11-10 | 2020-06-12 | 日本瑞翁株式会社 | Method and apparatus for regenerating cleaning solvent composition, and method and system for cleaning object to be cleaned |
TW202033573A (en) | 2018-12-17 | 2020-09-16 | 美商3M新設資產公司 | Composition including curable fluoropolymer and curative and methods of making and using them |
WO2020183306A1 (en) | 2019-03-12 | 2020-09-17 | 3M Innovative Properties Company | Dispersible perfluorosulfonic acid ionomer compositions |
US20220227696A1 (en) | 2019-06-04 | 2022-07-21 | 3M Innovative Properties Company | Multifunctional Fluorinated Compound, Fluorinated Polymers Made from the Compound, and Related Methods |
JP2023504273A (en) | 2019-12-02 | 2023-02-02 | スリーエム イノベイティブ プロパティズ カンパニー | Dispersible particles of perfluorosulfonic acid ionomer |
CN114901710B (en) | 2019-12-20 | 2024-01-30 | 3M创新有限公司 | Fluorinated copolymers and compositions and articles comprising the same |
US20230357172A1 (en) | 2020-03-19 | 2023-11-09 | 3M Innovative Properties Company | Perfluorinated Allyl Ethers and Perfluorinated Allyl Amines and Methods of Making and Using the Same |
EP4133542A1 (en) | 2020-04-09 | 2023-02-15 | 3M Innovative Properties Company | Composite including fluorinated polymer and salt nanoparticles and articles including the same |
WO2021214664A1 (en) | 2020-04-21 | 2021-10-28 | 3M Innovative Properties Company | Particles including polytetrafluoroethylene and process for making a three-dimensional article |
CN112591840B (en) * | 2020-11-26 | 2022-04-29 | 南京大学 | A kind of precipitation adsorption deep fluorine removal process of fluorine-containing water |
WO2022180547A1 (en) | 2021-02-26 | 2022-09-01 | 3M Innovative Properties Company | Process for making a fluoropolymer and fluoropolymer made therefrom |
WO2023057926A1 (en) | 2021-10-07 | 2023-04-13 | 3M Innovative Properties Company | Composite including fluorinated polymer and lithium fluoride nanoparticles and articles including the same |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3882153A (en) | 1969-09-12 | 1975-05-06 | Kureha Chemical Ind Co Ltd | Method for recovering fluorinated carboxylic acid |
GB1314607A (en) | 1969-09-12 | 1973-04-26 | Kureha Chemical Ind Co Ltd | Method for recovering perfluorinated emulsifiers |
DE2903981A1 (en) | 1979-02-02 | 1980-08-07 | Hoechst Ag | RECOVERY OF FLUORINATED EMULGATOR ACIDS FROM BASIC ANION EXCHANGERS |
DE2908001C2 (en) | 1979-03-01 | 1981-02-19 | Hoechst Ag, 6000 Frankfurt | Process for the preparation of concentrated dispersions of fluoropolymers |
US5017480A (en) * | 1987-08-10 | 1991-05-21 | Ajimomoto Co., Inc. | Process for recovering L-amino acid from fermentation liquors |
DE4213154C1 (en) * | 1992-04-22 | 1993-06-17 | Hoechst Ag, 6230 Frankfurt, De | |
DE4402694A1 (en) | 1993-06-02 | 1995-08-03 | Hoechst Ag | Process for the recovery of fluorinated carboxylic acids |
DE19824615A1 (en) * | 1998-06-02 | 1999-12-09 | Dyneon Gmbh | Process for the recovery of fluorinated alkanoic acids from waste water |
DE19824614A1 (en) * | 1998-06-02 | 1999-12-09 | Dyneon Gmbh | Process for the recovery of fluorinated alkanoic acids from waste water |
-
1999
- 1999-07-17 DE DE19933696A patent/DE19933696A1/en not_active Withdrawn
-
2000
- 2000-07-11 US US10/009,757 patent/US6706193B1/en not_active Expired - Fee Related
- 2000-07-11 TR TR2002/00135T patent/TR200200135T2/en unknown
- 2000-07-11 JP JP2001511374A patent/JP3820369B2/en not_active Expired - Fee Related
- 2000-07-11 KR KR10-2002-7000664A patent/KR100447479B1/en not_active IP Right Cessation
- 2000-07-11 ES ES00954467T patent/ES2173825T1/en active Pending
- 2000-07-11 AU AU66915/00A patent/AU767303B2/en not_active Ceased
- 2000-07-11 MX MXPA02000597A patent/MXPA02000597A/en not_active Application Discontinuation
- 2000-07-11 BR BR0012520-2A patent/BR0012520A/en not_active Application Discontinuation
- 2000-07-11 HU HU0201949A patent/HUP0201949A3/en unknown
- 2000-07-11 RU RU2002100912/15A patent/RU2248328C2/en not_active IP Right Cessation
- 2000-07-11 CN CNB00810428XA patent/CN1145587C/en not_active Expired - Fee Related
- 2000-07-11 EP EP00954467A patent/EP1208065A1/en not_active Ceased
- 2000-07-11 CZ CZ2002128A patent/CZ2002128A3/en unknown
- 2000-07-11 CA CA002379931A patent/CA2379931A1/en not_active Abandoned
- 2000-07-11 WO PCT/EP2000/006556 patent/WO2001005710A1/en active Search and Examination
- 2000-07-11 PL PL00364027A patent/PL364027A1/en unknown
- 2000-07-13 AR ARP000103601A patent/AR024730A1/en not_active Application Discontinuation
- 2000-07-13 TW TW089113945A patent/TW574151B/en not_active IP Right Cessation
- 2000-12-11 SA SA00210609A patent/SA00210609B1/en unknown
-
2002
- 2002-01-16 ZA ZA200200397A patent/ZA200200397B/en unknown
Non-Patent Citations (1)
Title |
---|
See references of WO0105710A1 * |
Also Published As
Publication number | Publication date |
---|---|
CN1145587C (en) | 2004-04-14 |
TW574151B (en) | 2004-02-01 |
AU767303B2 (en) | 2003-11-06 |
CZ2002128A3 (en) | 2002-10-16 |
RU2248328C2 (en) | 2005-03-20 |
PL364027A1 (en) | 2004-11-29 |
JP2003505223A (en) | 2003-02-12 |
CA2379931A1 (en) | 2001-01-25 |
JP3820369B2 (en) | 2006-09-13 |
US6706193B1 (en) | 2004-03-16 |
DE19933696A1 (en) | 2001-01-18 |
HUP0201949A3 (en) | 2003-01-28 |
KR100447479B1 (en) | 2004-09-07 |
AU6691500A (en) | 2001-02-05 |
ES2173825T1 (en) | 2002-11-01 |
MXPA02000597A (en) | 2003-07-21 |
BR0012520A (en) | 2002-04-02 |
SA00210609B1 (en) | 2006-08-22 |
CN1361751A (en) | 2002-07-31 |
WO2001005710A1 (en) | 2001-01-25 |
TR200200135T2 (en) | 2002-06-21 |
KR20020039322A (en) | 2002-05-25 |
AR024730A1 (en) | 2002-10-23 |
HUP0201949A2 (en) | 2002-11-28 |
ZA200200397B (en) | 2003-06-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2001005710A1 (en) | Method for recovering fluorinated emulsifiers from aqueous phases | |
EP1093441B1 (en) | Method for recovering fluorinated alkanoic acids from waste waters | |
DE60214343T2 (en) | Process for reducing the content of fluorinated emulsifiers in aqueous fluoropolymer dispersions | |
EP1155055B2 (en) | Aqueous dispersions of fluoropolymers | |
DE2908001C2 (en) | Process for the preparation of concentrated dispersions of fluoropolymers | |
DE60304469T2 (en) | METHOD FOR OBTAINING FLUOR-CONTAINING EMULSIFICATORS | |
DE602006000254T2 (en) | Process for the preparation of fluoropolymer dispersions | |
EP1353975B2 (en) | Method for the production of water-in-water polymer dispersions | |
DE602004004615T2 (en) | Process for the preparation of fluoropolymer dispersions | |
WO1995011269A1 (en) | Method of producing water-soluble polymer dispersions containing a high concentration of polymer | |
DE69407731T2 (en) | Removal of monomer residues | |
DE2044986C3 (en) | Process for the production of perfluorocarboxylic acids | |
DE19650316A1 (en) | Process for modifying the flow resistance of diaphragms | |
DE4309655C2 (en) | Process for the production of polyvinyl chloride resin for paste or plastisol production | |
DE69019342T2 (en) | Coagulation with thermal energy and washing of the latex particles. | |
EP0073296B2 (en) | Process for preparing dispersions of synthetic acrylic resins | |
DE60109119T2 (en) | Process for producing paraffin wax | |
DE69401714T2 (en) | METHOD FOR REMOVING ASH-FORMING RESIDUES FROM VINYL ALCOHOL POLYMERS | |
DE2203465C2 (en) | Process for the preparation of aqueous dispersions of polytetrafluoroethylene | |
DE4118526A1 (en) | Removing residual monomers etc. from aq. polymer dispersions - by passing through the dispersion a stream of inert gas contg. specified vol. of water to gas | |
DE2733272A1 (en) | PROCESS FOR SEPARATING A LOW MOLECULAR POLYMERIZED WITH A VISCOSITY OF 5 TO 100,000 CP AT 30 DEGREE CELSIUS FROM A SOLUTION CONTAINING THIS POLYMERIZED AND AN INACTIVATED CATALYST | |
DE1454874A1 (en) | Process for the preparation of strongly basic anion exchange resin particles | |
DE69406318T2 (en) | Process for the electrolysis of an alkali metal chloride | |
DE1254592B (en) | Process to improve the filterability of aqueous organic slimes | |
EP2239276A1 (en) | Use of anionic tensides as emulgators for emulsion polymerisation III |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20011211 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
TCNL | Nl: translation of patent claims filed | ||
17Q | First examination report despatched |
Effective date: 20020625 |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: PP Ref document number: 20020300021 Country of ref document: GR |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: BA2A Ref document number: 2173825 Country of ref document: ES Kind code of ref document: T1 |
|
APBN | Date of receipt of notice of appeal recorded |
Free format text: ORIGINAL CODE: EPIDOSNNOA2E |
|
APBR | Date of receipt of statement of grounds of appeal recorded |
Free format text: ORIGINAL CODE: EPIDOSNNOA3E |
|
APAA | Appeal reference recorded |
Free format text: ORIGINAL CODE: EPIDOS REFN |
|
APAF | Appeal reference modified |
Free format text: ORIGINAL CODE: EPIDOSCREFNE |
|
APAM | Information on closure of appeal procedure modified |
Free format text: ORIGINAL CODE: EPIDOSCNOA9E |
|
APBT | Appeal procedure closed |
Free format text: ORIGINAL CODE: EPIDOSNNOA9E |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED |
|
18R | Application refused |
Effective date: 20060817 |