FI65268C - Foerfarande foer framstaellning av organiska polymerer genom ultraviolettbestraolning av en vattenloesning av monomerer - Google Patents
Foerfarande foer framstaellning av organiska polymerer genom ultraviolettbestraolning av en vattenloesning av monomerer Download PDFInfo
- Publication number
- FI65268C FI65268C FI791814A FI791814A FI65268C FI 65268 C FI65268 C FI 65268C FI 791814 A FI791814 A FI 791814A FI 791814 A FI791814 A FI 791814A FI 65268 C FI65268 C FI 65268C
- Authority
- FI
- Finland
- Prior art keywords
- solution
- photopolymerization
- irradiation
- process according
- monomers
- Prior art date
Links
- 239000000178 monomer Substances 0.000 claims description 36
- 239000000243 solution Substances 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- 230000005855 radiation Effects 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 3
- 229920000620 organic polymer Polymers 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 10
- 239000011521 glass Substances 0.000 description 9
- 238000001914 filtration Methods 0.000 description 8
- 239000008394 flocculating agent Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- -1 acyl amide ester Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 241000234282 Allium Species 0.000 description 4
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 4
- 238000007922 dissolution test Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000003311 flocculating effect Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000005587 bubbling Effects 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 229920003169 water-soluble polymer Polymers 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 2
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical group [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical class CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S522/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S522/903—Removal of residual monomer
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7817857 | 1978-06-09 | ||
| FR7817857A FR2428053A2 (fr) | 1978-06-09 | 1978-06-09 | Procede de photopolymerisation pour polymeres floculants |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI791814A FI791814A (fi) | 1979-12-10 |
| FI65268B FI65268B (fi) | 1983-12-30 |
| FI65268C true FI65268C (fi) | 1984-04-10 |
Family
ID=9209528
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI791814A FI65268C (fi) | 1978-06-09 | 1979-06-06 | Foerfarande foer framstaellning av organiska polymerer genom ultraviolettbestraolning av en vattenloesning av monomerer |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4252625A (hu) |
| EP (1) | EP0006777B1 (hu) |
| JP (1) | JPS608681B2 (hu) |
| AT (1) | AT369390B (hu) |
| AU (1) | AU525520B2 (hu) |
| BR (1) | BR7903567A (hu) |
| CA (1) | CA1122920A (hu) |
| DE (1) | DE2960983D1 (hu) |
| DK (1) | DK154506C (hu) |
| ES (1) | ES481385A1 (hu) |
| FI (1) | FI65268C (hu) |
| FR (1) | FR2428053A2 (hu) |
| HU (1) | HU181491B (hu) |
| NO (1) | NO153733C (hu) |
| RO (1) | RO78267A (hu) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2489336B1 (fr) * | 1980-09-04 | 1985-09-13 | Rhone Poulenc Spec Chim | Procede de preparation de polymeres ou copolymeres hydrosolubles a poids moleculaire eleve et a faible teneur en monomere(s) residuel(s), a partir de monomeres olefiniquement insatures |
| JPS60152504A (ja) * | 1984-01-19 | 1985-08-10 | Dai Ichi Kogyo Seiyaku Co Ltd | 粘着性重合体の製法 |
| CA1268732C (en) * | 1984-12-27 | 1990-05-08 | POLYMERIZATION BY RADIATION AND OBTAINING PARTICLES BY CASTING A LAYER OF WATER-SOLUBLE VINYL MONOMER | |
| JP2545951B2 (ja) * | 1988-09-26 | 1996-10-23 | 東亞合成株式会社 | 光硬化性組成物 |
| US5244934A (en) * | 1991-06-07 | 1993-09-14 | Takai Rubber Industries, Ltd. | Irradiation or thermal treatment of water-impregnated cross-linked poly-acrylic acid metal salt resin particles |
| US6262141B1 (en) | 1999-10-06 | 2001-07-17 | Cytec Technology Corporation | Process for the preparation of polymers having low residual monomer content |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB654026A (en) * | 1948-10-22 | 1951-05-30 | John Patrick Cavanagh | Polymeric compositions intended for moulding or extrusion |
| US2937163A (en) * | 1955-03-07 | 1960-05-17 | Dow Chemical Co | Water-soluble polymerization products and processes for producing the same |
| NL130574C (hu) * | 1966-06-25 | |||
| US3912607A (en) * | 1969-10-22 | 1975-10-14 | Rhone Progil | Process for obtaining high molecular weight water-soluble acrylic polymers and copolymers using radiation |
| DE2009748A1 (de) * | 1970-03-03 | 1971-09-16 | Basf Ag | Verfahren zur Herstellung von wasser löslichen Polymerisaten |
| JPS5141160B2 (hu) * | 1974-08-13 | 1976-11-08 | ||
| DE2545290A1 (de) * | 1975-10-09 | 1977-04-21 | Roehm Gmbh | Verfahren zum polymerisieren mittels uv-licht |
| DE2546279A1 (de) * | 1975-10-16 | 1977-04-21 | Bayer Ag | Verfahren und vorrichtung zum loesen von feststoffen in loesungsmitteln |
| FR2348227A1 (fr) * | 1976-04-14 | 1977-11-10 | Rhone Poulenc Ind | Perfectionnement aux procedes de preparation de polymeres acryliques hydrosolubles par photopolymerisation |
| JPS54155296A (en) * | 1978-05-29 | 1979-12-07 | Sanyo Chem Ind Ltd | Preparation of water-soluble polymer |
-
1978
- 1978-06-09 FR FR7817857A patent/FR2428053A2/fr active Granted
-
1979
- 1979-05-30 EP EP79400341A patent/EP0006777B1/fr not_active Expired
- 1979-05-30 DE DE7979400341T patent/DE2960983D1/de not_active Expired
- 1979-06-06 BR BR7903567A patent/BR7903567A/pt not_active IP Right Cessation
- 1979-06-06 FI FI791814A patent/FI65268C/fi not_active IP Right Cessation
- 1979-06-06 HU HU79RO1024A patent/HU181491B/hu unknown
- 1979-06-07 NO NO791906A patent/NO153733C/no unknown
- 1979-06-07 AU AU47843/79A patent/AU525520B2/en not_active Ceased
- 1979-06-07 US US06/046,489 patent/US4252625A/en not_active Expired - Lifetime
- 1979-06-08 CA CA329,387A patent/CA1122920A/fr not_active Expired
- 1979-06-08 DK DK239479A patent/DK154506C/da not_active IP Right Cessation
- 1979-06-08 AT AT0414079A patent/AT369390B/de not_active IP Right Cessation
- 1979-06-08 JP JP54071332A patent/JPS608681B2/ja not_active Expired
- 1979-06-08 ES ES481385A patent/ES481385A1/es not_active Expired
- 1979-06-09 RO RO7997786A patent/RO78267A/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA1122920A (fr) | 1982-05-04 |
| RO78267A (ro) | 1982-04-12 |
| BR7903567A (pt) | 1980-01-22 |
| NO153733C (no) | 1986-05-14 |
| FR2428053A2 (fr) | 1980-01-04 |
| EP0006777B1 (fr) | 1981-10-14 |
| DE2960983D1 (en) | 1981-12-24 |
| FR2428053B2 (hu) | 1984-07-20 |
| DK154506B (da) | 1988-11-21 |
| ATA414079A (de) | 1982-05-15 |
| NO791906L (no) | 1979-12-11 |
| DK154506C (da) | 1989-04-10 |
| AU525520B2 (en) | 1982-11-11 |
| HU181491B (en) | 1983-07-28 |
| JPS608681B2 (ja) | 1985-03-05 |
| JPS559687A (en) | 1980-01-23 |
| FI791814A (fi) | 1979-12-10 |
| AU4784379A (en) | 1979-12-13 |
| NO153733B (no) | 1986-02-03 |
| AT369390B (de) | 1982-12-27 |
| US4252625A (en) | 1981-02-24 |
| DK239479A (da) | 1979-12-10 |
| FI65268B (fi) | 1983-12-30 |
| EP0006777A1 (fr) | 1980-01-09 |
| ES481385A1 (es) | 1979-11-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: RHONE- POULENC INDUSTRIES |