NO753931L - - Google Patents
Info
- Publication number
- NO753931L NO753931L NO753931A NO753931A NO753931L NO 753931 L NO753931 L NO 753931L NO 753931 A NO753931 A NO 753931A NO 753931 A NO753931 A NO 753931A NO 753931 L NO753931 L NO 753931L
- Authority
- NO
- Norway
- Prior art keywords
- acrylonitrile
- temperature
- stated
- polymer particles
- raised
- Prior art date
Links
- 238000000034 method Methods 0.000 claims abstract description 51
- 239000000178 monomer Substances 0.000 claims abstract description 35
- 229920002239 polyacrylonitrile Polymers 0.000 claims abstract description 12
- 230000008569 process Effects 0.000 claims abstract description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 45
- 229920000642 polymer Polymers 0.000 claims description 43
- 229920001577 copolymer Polymers 0.000 claims description 22
- 239000002245 particle Substances 0.000 claims description 21
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 15
- 230000009477 glass transition Effects 0.000 claims description 14
- 238000006116 polymerization reaction Methods 0.000 claims description 11
- 239000006185 dispersion Substances 0.000 claims description 9
- 125000005396 acrylic acid ester group Chemical group 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 4
- 230000008018 melting Effects 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 150000008360 acrylonitriles Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 235000013361 beverage Nutrition 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920006301 statistical copolymer Polymers 0.000 description 2
- 150000003440 styrenes Chemical class 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- XHAFIUUYXQFJEW-UHFFFAOYSA-N 1-chloroethenylbenzene Chemical compound ClC(=C)C1=CC=CC=C1 XHAFIUUYXQFJEW-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920001198 elastomeric copolymer Polymers 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000012685 gas phase polymerization Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- -1 maleic acid Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- C08F6/00—Post-polymerisation treatments
- C08F6/001—Removal of residual monomers by physical means
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7438780A FR2291987A1 (fr) | 1974-11-25 | 1974-11-25 | Procede pour l'elimination des residus de monomere dans les polymeres de l'acrylonitrile |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO753931L true NO753931L (he) | 1976-05-26 |
Family
ID=9145270
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO753931A NO753931L (he) | 1974-11-25 | 1975-11-21 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4197400A (he) |
| JP (1) | JPS5176380A (he) |
| AT (1) | AT343901B (he) |
| BE (1) | BE835673A (he) |
| BR (1) | BR7507322A (he) |
| CA (1) | CA1067248A (he) |
| CH (1) | CH596247A5 (he) |
| DE (1) | DE2547140A1 (he) |
| DK (1) | DK527875A (he) |
| ES (1) | ES442025A1 (he) |
| FI (1) | FI59604C (he) |
| FR (1) | FR2291987A1 (he) |
| GB (1) | GB1480555A (he) |
| IE (1) | IE42104B1 (he) |
| IT (1) | IT1043187B (he) |
| LU (1) | LU73823A1 (he) |
| NL (1) | NL7512913A (he) |
| NO (1) | NO753931L (he) |
| SE (1) | SE7513165L (he) |
| SU (1) | SU646917A3 (he) |
| ZA (1) | ZA756434B (he) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4174043A (en) * | 1977-11-10 | 1979-11-13 | Monsanto Company | Nitrile preforms and containers and process improvements for forming same |
| DE2804533C2 (de) * | 1978-02-03 | 1985-05-23 | Röhm GmbH, 6100 Darmstadt | Verfahren zur Herstellung restmonomerarmer Mischpolymerisate des Acrylnitrils und ihre Verwendung zur Herstellung orthopädischer Formkörper |
| US4206300A (en) * | 1978-06-12 | 1980-06-03 | Standand Oil Company | Method for improving color and impact strength of nitrile polymers |
| IT1198338B (it) * | 1980-07-02 | 1988-12-21 | Montedison Spa | Processo per produrre copolimeri di monomeri vinil-aromatici con nitrili etilenicamente insaturi |
| US4396740A (en) * | 1982-05-03 | 1983-08-02 | Borg-Warner Chemicals, Inc. | Scavenging of residual acrylonitrile monomer in ABS latex |
| JPS59191704A (ja) * | 1983-04-13 | 1984-10-30 | Japan Exlan Co Ltd | 高分子量アクリロニトリル系重合体の製造法 |
| US4517347A (en) * | 1984-07-25 | 1985-05-14 | Westvaco Corporation | Method for copolymerization of styrene and acrylonitrile |
| NL8403488A (nl) * | 1984-11-15 | 1986-06-02 | Stamicarbon | Werkwijze voor de zuivering van een acrylonitrilgroepen bevattend copolymeer. |
| JP3650975B2 (ja) * | 1995-07-28 | 2005-05-25 | 日本エクスラン工業株式会社 | 改善されたアクリロニトリル系重合体溶融物の 製造方法 |
| DE60015672T2 (de) * | 1999-08-27 | 2005-12-01 | Rohm And Haas Co. | Verfahren zum Abstrippen von Polymerdispersionen oder Polymerlösungen |
| DE10031766A1 (de) * | 2000-06-29 | 2002-01-10 | Bayer Ag | Kautschukfreie Copolymerisate mit niedrigen Monomerrestgehalten und Verfahren und Vorrichtung zu ihrer Herstellung |
| DE10357160A1 (de) * | 2003-12-06 | 2005-07-07 | Bayer Materialscience Ag | Verfahren zur Aufarbeitung von Polymerdispersionen in Polyesterpolyolen |
| JP4867234B2 (ja) * | 2005-08-24 | 2012-02-01 | 東亞合成株式会社 | 高粘度低臭気エマルションの製造方法 |
| JP5002930B2 (ja) * | 2005-09-13 | 2012-08-15 | 東亞合成株式会社 | 低臭気エマルションの製造方法 |
| ES2685302T3 (es) * | 2014-04-30 | 2018-10-08 | Ineos Styrolution Group Gmbh | Masas moldeadas termoplásticas con contenido optimizado de monómeros residuales |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE532139A (he) * | 1953-09-29 | |||
| NL211766A (he) * | 1955-10-31 | |||
| GB1048013A (en) * | 1962-07-11 | 1966-11-09 | Asahi Chemical Ind | Method of recovering acrylonitrile monomer |
| NL147157B (nl) * | 1963-10-17 | 1975-09-15 | Edison Soc | Werkwijze om terpolymeren te bereiden. |
| NL129660C (he) * | 1964-08-24 | |||
| FR1445145A (fr) * | 1964-08-24 | 1966-07-08 | Monsanto Co | Récupération des monomères non polymérisés d'une bouillie polymère |
| US3325457A (en) * | 1965-08-26 | 1967-06-13 | Foster Grant Co Inc | Method of preparing acrylonitrile polymers |
| US3663631A (en) * | 1970-04-24 | 1972-05-16 | American Cyanamid Co | Method of recovering unreacted monomers |
| US3663632A (en) * | 1970-05-13 | 1972-05-16 | American Cyanamid Co | Method of recovering unreacted monomers |
-
1974
- 1974-11-25 FR FR7438780A patent/FR2291987A1/fr active Granted
-
1975
- 1975-10-07 IT IT28051/75A patent/IT1043187B/it active
- 1975-10-13 ZA ZA00756434A patent/ZA756434B/xx unknown
- 1975-10-21 DE DE19752547140 patent/DE2547140A1/de not_active Withdrawn
- 1975-10-23 ES ES442025A patent/ES442025A1/es not_active Expired
- 1975-10-24 FI FI752975A patent/FI59604C/fi not_active IP Right Cessation
- 1975-10-28 GB GB44295/75A patent/GB1480555A/en not_active Expired
- 1975-11-04 NL NL7512913A patent/NL7512913A/xx not_active Application Discontinuation
- 1975-11-06 US US05/629,540 patent/US4197400A/en not_active Expired - Lifetime
- 1975-11-06 BR BR7507322*A patent/BR7507322A/pt unknown
- 1975-11-11 CH CH1460575A patent/CH596247A5/xx not_active IP Right Cessation
- 1975-11-14 IE IE2491/75A patent/IE42104B1/en unknown
- 1975-11-18 BE BE161952A patent/BE835673A/xx unknown
- 1975-11-18 LU LU73823A patent/LU73823A1/xx unknown
- 1975-11-21 NO NO753931A patent/NO753931L/no unknown
- 1975-11-24 SE SE7513165A patent/SE7513165L/ not_active Application Discontinuation
- 1975-11-24 SU SU752193149A patent/SU646917A3/ru active
- 1975-11-24 CA CA240,324A patent/CA1067248A/fr not_active Expired
- 1975-11-24 DK DK527875A patent/DK527875A/da not_active Application Discontinuation
- 1975-11-24 AT AT891575A patent/AT343901B/de not_active IP Right Cessation
- 1975-11-25 JP JP50140357A patent/JPS5176380A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA1067248A (fr) | 1979-11-27 |
| DE2547140A1 (de) | 1976-08-12 |
| FI59604B (fi) | 1981-05-29 |
| SE7513165L (sv) | 1976-05-26 |
| AT343901B (de) | 1978-06-26 |
| FI59604C (fi) | 1981-09-10 |
| LU73823A1 (he) | 1976-09-06 |
| GB1480555A (en) | 1977-07-20 |
| JPS5176380A (he) | 1976-07-01 |
| ZA756434B (en) | 1976-09-29 |
| US4197400A (en) | 1980-04-08 |
| CH596247A5 (he) | 1978-03-15 |
| FR2291987A1 (fr) | 1976-06-18 |
| BE835673A (fr) | 1976-05-18 |
| IE42104L (en) | 1976-05-25 |
| FR2291987B1 (he) | 1977-03-25 |
| ATA891575A (de) | 1977-10-15 |
| BR7507322A (pt) | 1976-08-10 |
| NL7512913A (nl) | 1976-05-28 |
| FI752975A (he) | 1976-05-26 |
| DK527875A (da) | 1976-05-26 |
| SU646917A3 (ru) | 1979-02-05 |
| IT1043187B (it) | 1980-02-20 |
| ES442025A1 (es) | 1977-03-16 |
| AU8607075A (en) | 1977-05-05 |
| IE42104B1 (en) | 1980-06-04 |
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