DE3544206C2 - - Google Patents
Info
- Publication number
- DE3544206C2 DE3544206C2 DE3544206A DE3544206A DE3544206C2 DE 3544206 C2 DE3544206 C2 DE 3544206C2 DE 3544206 A DE3544206 A DE 3544206A DE 3544206 A DE3544206 A DE 3544206A DE 3544206 C2 DE3544206 C2 DE 3544206C2
- Authority
- DE
- Germany
- Prior art keywords
- chlorotrifluoroethylene
- volume
- percent
- ethylene
- porous membrane
- 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.)
- Expired
Links
- 239000012528 membrane Substances 0.000 claims description 164
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims description 84
- 239000000203 mixture Substances 0.000 claims description 45
- 239000000463 material Substances 0.000 claims description 44
- 239000011148 porous material Substances 0.000 claims description 42
- -1 ethylene-chlorotrifluoroethylene Chemical group 0.000 claims description 41
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 34
- 229920005989 resin Polymers 0.000 claims description 34
- 239000011347 resin Substances 0.000 claims description 34
- 239000000126 substance Substances 0.000 claims description 34
- 238000000605 extraction Methods 0.000 claims description 32
- 229920002313 fluoropolymer Polymers 0.000 claims description 29
- 239000004811 fluoropolymer Substances 0.000 claims description 29
- 239000012510 hollow fiber Substances 0.000 claims description 28
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 claims description 26
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 claims description 26
- 239000010419 fine particle Substances 0.000 claims description 19
- 229920001780 ECTFE Polymers 0.000 claims description 18
- 230000008569 process Effects 0.000 claims description 16
- 238000000137 annealing Methods 0.000 claims description 14
- 230000008018 melting Effects 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 12
- 239000000835 fiber Substances 0.000 claims description 10
- 238000005496 tempering Methods 0.000 claims description 9
- 239000000155 melt Substances 0.000 claims description 7
- 229920002545 silicone oil Polymers 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 6
- CHJAYYWUZLWNSQ-UHFFFAOYSA-N 1-chloro-1,2,2-trifluoroethene;ethene Chemical group C=C.FC(F)=C(F)Cl CHJAYYWUZLWNSQ-UHFFFAOYSA-N 0.000 claims description 4
- 238000000465 moulding Methods 0.000 claims description 3
- VUGHUBKRIVNEJQ-UHFFFAOYSA-N FC=C(F)F.[Cl] Chemical group FC=C(F)F.[Cl] VUGHUBKRIVNEJQ-UHFFFAOYSA-N 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 44
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- 239000000377 silicon dioxide Substances 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 229920001296 polysiloxane Polymers 0.000 description 18
- 229910002012 Aerosil® Inorganic materials 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 17
- 230000009467 reduction Effects 0.000 description 17
- 238000002156 mixing Methods 0.000 description 14
- 235000012239 silicon dioxide Nutrition 0.000 description 14
- 239000002245 particle Substances 0.000 description 13
- 239000000843 powder Substances 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 12
- 230000035699 permeability Effects 0.000 description 12
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 11
- 239000008188 pellet Substances 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 230000008859 change Effects 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000005416 organic matter Substances 0.000 description 7
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 239000002952 polymeric resin Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920004428 Neoflon® PCTFE Polymers 0.000 description 2
- KRADHMIOFJQKEZ-UHFFFAOYSA-N Tri-2-ethylhexyl trimellitate Chemical compound CCCCC(CC)COC(=O)C1=CC=C(C(=O)OCC(CC)CCCC)C(C(=O)OCC(CC)CCCC)=C1 KRADHMIOFJQKEZ-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000000378 calcium silicate Substances 0.000 description 2
- 229910052918 calcium silicate Inorganic materials 0.000 description 2
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 239000010702 perfluoropolyether Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000000992 sputter etching Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 125000005590 trimellitic acid group Chemical class 0.000 description 2
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 description 1
- 229920004435 Aclon® Polymers 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 244000287680 Garcinia dulcis Species 0.000 description 1
- 229920006360 Hostaflon Polymers 0.000 description 1
- 229920004459 Kel-F® PCTFE Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 229920006355 Tefzel Polymers 0.000 description 1
- 229920004463 Voltalef® Polymers 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001278 adipic acid derivatives Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001535 azelaic acid derivatives Chemical class 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- QHSJIZLJUFMIFP-UHFFFAOYSA-N ethene;1,1,2,2-tetrafluoroethene Chemical compound C=C.FC(F)=C(F)F QHSJIZLJUFMIFP-UHFFFAOYSA-N 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 150000003329 sebacic acid derivatives Chemical class 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/26—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a solid phase from a macromolecular composition or article, e.g. leaching out
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
- B01D67/0025—Organic membrane manufacture by inducing porosity into non porous precursor membranes by mechanical treatment, e.g. pore-stretching
- B01D67/0027—Organic membrane manufacture by inducing porosity into non porous precursor membranes by mechanical treatment, e.g. pore-stretching by stretching
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
- B01D67/003—Organic membrane manufacture by inducing porosity into non porous precursor membranes by selective elimination of components, e.g. by leaching
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/30—Polyalkenyl halides
- B01D71/32—Polyalkenyl halides containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2201/00—Foams characterised by the foaming process
- C08J2201/04—Foams characterised by the foaming process characterised by the elimination of a liquid or solid component, e.g. precipitation, leaching out, evaporation
- C08J2201/044—Elimination of an inorganic solid phase
- C08J2201/0442—Elimination of an inorganic solid phase the inorganic phase being a metal, its oxide or hydroxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27392084A JPS61152739A (ja) | 1984-12-27 | 1984-12-27 | エチレン−テトラフルオロエチレン共重合体多孔膜の製造方法 |
| JP7347185A JPS61233026A (ja) | 1985-04-09 | 1985-04-09 | 多孔膜の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3544206A1 DE3544206A1 (de) | 1986-07-10 |
| DE3544206C2 true DE3544206C2 (enExample) | 1988-10-20 |
Family
ID=26414619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19853544206 Granted DE3544206A1 (de) | 1984-12-27 | 1985-12-13 | Poroese membran aus einem fluorpolymerharz und verfahren zu ihrer herstellung |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US4623670A (enExample) |
| DE (1) | DE3544206A1 (enExample) |
| FR (1) | FR2575480B1 (enExample) |
| GB (1) | GB2168981B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3928934C1 (enExample) * | 1989-08-31 | 1990-10-11 | Sartorius Gmbh, 3400 Goettingen, De | |
| WO1993005866A1 (en) * | 1991-09-13 | 1993-04-01 | The Dow Chemical Company | Semi-permeable membranes derived from reactive oligomers |
Families Citing this family (112)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2219589A (en) * | 1988-06-13 | 1989-12-13 | Scimat Ltd | Microporous halopolymer films |
| US5198162A (en) * | 1984-12-19 | 1993-03-30 | Scimat Limited | Microporous films |
| GB2168981B (en) * | 1984-12-27 | 1988-07-06 | Asahi Chemical Ind | Porous fluorine resin membrane and process for preparation thereof |
| US4980060A (en) * | 1987-07-13 | 1990-12-25 | Asahi Kasei Kogyo Kabushiki Kaisha | Hollow fiber membranes with fusion-bonded end portions |
| US4902456A (en) * | 1988-05-04 | 1990-02-20 | Millipore Corporation | Fluorocarbon membranes and process for making fluorocarbon membranes |
| US5032274A (en) * | 1988-05-04 | 1991-07-16 | Millipore Corporation | Process for producing fluorocarbon membranes and membrane product |
| US4906377A (en) * | 1988-05-04 | 1990-03-06 | Millipore Corporation | Fluorocarbon membranes and process for making fluorocarbon membranes |
| US4997603A (en) * | 1988-08-05 | 1991-03-05 | Hoechst Celanese Corp. | Process for formation of halogenated polymeric microporous membranes having improved strength properties |
| US5043113A (en) * | 1988-08-05 | 1991-08-27 | Hoechst Celanese Corp. | Process for formation of halogenated polymeric microporous membranes having improved strength properties |
| US4873037A (en) * | 1988-10-05 | 1989-10-10 | The Dow Chemical Company | Method for preparing an asymmetric semi-permeable membrane |
| US5022990A (en) * | 1989-01-12 | 1991-06-11 | Asahi Kasei Kogyo Kabushiki Kaisha | Polyvinylidene fluoride porous membrane and a method for producing the same |
| GB2232982A (en) * | 1989-06-13 | 1991-01-02 | Scimat Ltd | Microporous films |
| FR2682613B1 (fr) * | 1991-10-22 | 1994-06-03 | Cogia | Procede de deshydratation au moins partielle d'une composition aqueuse et dispositifs pour mettre en óoeuvre le procede. |
| US5358780A (en) * | 1992-04-01 | 1994-10-25 | Hoechst Celanese Corp. | Breathable water-resistant fabrics |
| DE4424466A1 (de) * | 1994-07-12 | 1996-01-18 | Hoechst Ag | Copolymeres vom Typ Tetrafluorethylen-Ethylen mit einer Kern-Hülle-Teilchenstruktur |
| US5614319A (en) * | 1995-05-04 | 1997-03-25 | Commscope, Inc. | Insulating composition, insulated plenum cable and methods for making same |
| EP0750006B1 (en) * | 1995-06-23 | 2002-03-27 | Technische Universiteit Delft | Method of making a foamable film |
| WO1998028066A1 (en) | 1996-12-20 | 1998-07-02 | Usf Filtration And Separations Group, Inc. | Scouring method |
| FR2759087B1 (fr) * | 1997-02-06 | 1999-07-30 | Electricite De France | Produit composite poreux de haute surface specifique, procede de preparation et electrode pour ensemble electrochimique formee d'un film composite poreux |
| AU2001264604A1 (en) * | 2000-05-16 | 2001-11-26 | Watervisions International, Inc. | Filter devices and methods of use |
| AUPR143400A0 (en) | 2000-11-13 | 2000-12-07 | Usf Filtration And Separations Group Inc. | Modified membranes |
| ITMI20010421A1 (it) | 2001-03-01 | 2002-09-02 | Ausimont Spa | Membrane porose semipermeabili di fluoropolimeri semicristallini |
| JP4043364B2 (ja) * | 2001-03-06 | 2008-02-06 | 旭化成ケミカルズ株式会社 | 中空糸膜の製造方法 |
| AUPR421501A0 (en) | 2001-04-04 | 2001-05-03 | U.S. Filter Wastewater Group, Inc. | Potting method |
| AUPR584301A0 (en) * | 2001-06-20 | 2001-07-12 | U.S. Filter Wastewater Group, Inc. | Membrane polymer compositions |
| AUPR692401A0 (en) | 2001-08-09 | 2001-08-30 | U.S. Filter Wastewater Group, Inc. | Method of cleaning membrane modules |
| AUPS046602A0 (en) * | 2002-02-12 | 2002-03-07 | U.S. Filter Wastewater Group, Inc. | Halar membranes |
| US7247238B2 (en) | 2002-02-12 | 2007-07-24 | Siemens Water Technologies Corp. | Poly(ethylene chlorotrifluoroethylene) membranes |
| AUPS300602A0 (en) | 2002-06-18 | 2002-07-11 | U.S. Filter Wastewater Group, Inc. | Methods of minimising the effect of integrity loss in hollow fibre membrane modules |
| KR101002466B1 (ko) | 2002-10-10 | 2010-12-17 | 지멘스 워터 테크놀로지스 코포레이션 | 역세척 방법 |
| DE10257093B4 (de) * | 2002-12-05 | 2005-02-24 | Basf Ag | Aerosolabscheider und Verfahren zur Reinigung von gasförmigem Schwefeltrioxid durch Abscheidung darin dispergierter Flüssigkeiten |
| AU2002953111A0 (en) | 2002-12-05 | 2002-12-19 | U. S. Filter Wastewater Group, Inc. | Mixing chamber |
| US7081208B2 (en) * | 2002-12-16 | 2006-07-25 | International Business Machines Corporation | Method to build a microfilter |
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| US2915483A (en) | 1953-12-30 | 1959-12-01 | Minnesota Mining & Mfg | Plasticized perfluorochloroethylene polymer and process for preparing porous articles therefrom |
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| DE1769595C3 (de) * | 1968-06-12 | 1975-07-17 | Robert Bosch Gmbh, 7000 Stuttgart | Verfahren zur Herstellung von gasdurchlässigen, hydrophoben Folien aus fluorhaltigen Polymeren für elektrochemische Zellen, insbesondere Brennstoffzellen |
| US4181983A (en) | 1977-08-29 | 1980-01-08 | Kulkarni R K | Assimilable hydrophilic prosthesis |
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| JPS56159128A (en) * | 1980-05-15 | 1981-12-08 | Asahi Chem Ind Co Ltd | Thermoplastic resin porous film and production thereof |
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| GB2168981B (en) * | 1984-12-27 | 1988-07-06 | Asahi Chemical Ind | Porous fluorine resin membrane and process for preparation thereof |
-
1985
- 1985-12-05 GB GB08530028A patent/GB2168981B/en not_active Expired
- 1985-12-13 DE DE19853544206 patent/DE3544206A1/de active Granted
- 1985-12-13 US US06/808,491 patent/US4623670A/en not_active Expired - Lifetime
- 1985-12-13 FR FR858518516A patent/FR2575480B1/fr not_active Expired
-
1986
- 1986-07-11 US US06/884,519 patent/US4702836A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3928934C1 (enExample) * | 1989-08-31 | 1990-10-11 | Sartorius Gmbh, 3400 Goettingen, De | |
| DE3928934C2 (de) * | 1989-08-31 | 1999-04-29 | Sartorius Gmbh | Textilverstärktes mikroporöses Membranfilter, Verfahren zu seiner Herstellung und seine Verwendung |
| WO1993005866A1 (en) * | 1991-09-13 | 1993-04-01 | The Dow Chemical Company | Semi-permeable membranes derived from reactive oligomers |
Also Published As
| Publication number | Publication date |
|---|---|
| GB8530028D0 (en) | 1986-01-15 |
| US4702836A (en) | 1987-10-27 |
| GB2168981A (en) | 1986-07-02 |
| FR2575480B1 (fr) | 1989-12-22 |
| GB2168981B (en) | 1988-07-06 |
| US4623670A (en) | 1986-11-18 |
| DE3544206A1 (de) | 1986-07-10 |
| FR2575480A1 (fr) | 1986-07-04 |
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