DE2040094C3 - Verfahren zur Herstellung von Bis-maleinimiden - Google Patents
Verfahren zur Herstellung von Bis-maleinimidenInfo
- Publication number
- DE2040094C3 DE2040094C3 DE2040094A DE2040094A DE2040094C3 DE 2040094 C3 DE2040094 C3 DE 2040094C3 DE 2040094 A DE2040094 A DE 2040094A DE 2040094 A DE2040094 A DE 2040094A DE 2040094 C3 DE2040094 C3 DE 2040094C3
- Authority
- DE
- Germany
- Prior art keywords
- bis
- acid
- maleamic
- maleamic acid
- per mole
- 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
- 238000000034 method Methods 0.000 title claims description 10
- 238000002360 preparation method Methods 0.000 title claims description 4
- 239000002253 acid Substances 0.000 claims description 17
- 150000007513 acids Chemical class 0.000 claims description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 8
- 150000003512 tertiary amines Chemical class 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- 150000002576 ketones Chemical class 0.000 claims description 5
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000006227 byproduct Substances 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- -1 cycloaliphatic Chemical group 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000003756 stirring Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- 239000011976 maleic acid Substances 0.000 description 5
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical class O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 229940078487 nickel acetate tetrahydrate Drugs 0.000 description 3
- OINIXPNQKAZCRL-UHFFFAOYSA-L nickel(2+);diacetate;tetrahydrate Chemical compound O.O.O.O.[Ni+2].CC([O-])=O.CC([O-])=O OINIXPNQKAZCRL-UHFFFAOYSA-L 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- FSQQTNAZHBEJLS-UPHRSURJSA-N maleamic acid Chemical compound NC(=O)\C=C/C(O)=O FSQQTNAZHBEJLS-UPHRSURJSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002815 nickel Chemical class 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 241000218195 Lauraceae Species 0.000 description 1
- 235000017858 Laurus nobilis Nutrition 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000005212 Terminalia tomentosa Nutrition 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000006210 cyclodehydration reaction Methods 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- BMGNSKKZFQMGDH-FDGPNNRMSA-L nickel(2+);(z)-4-oxopent-2-en-2-olate Chemical compound [Ni+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O BMGNSKKZFQMGDH-FDGPNNRMSA-L 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
- C07D207/448—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyrrole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR6927717A FR2055969A5 (enExample) | 1969-08-12 | 1969-08-12 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2040094A1 DE2040094A1 (de) | 1971-03-11 |
| DE2040094B2 DE2040094B2 (de) | 1974-05-02 |
| DE2040094C3 true DE2040094C3 (de) | 1974-12-12 |
Family
ID=9038968
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2040094A Expired DE2040094C3 (de) | 1969-08-12 | 1970-08-12 | Verfahren zur Herstellung von Bis-maleinimiden |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3839358A (enExample) |
| JP (1) | JPS4940231B1 (enExample) |
| AT (1) | AT294065B (enExample) |
| BE (1) | BE754723A (enExample) |
| CH (1) | CH514585A (enExample) |
| DE (1) | DE2040094C3 (enExample) |
| FR (1) | FR2055969A5 (enExample) |
| GB (1) | GB1276446A (enExample) |
| LU (1) | LU61500A1 (enExample) |
| NL (1) | NL149163B (enExample) |
| SE (1) | SE368200B (enExample) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2153331B1 (enExample) * | 1971-09-21 | 1975-03-14 | Union Carbide Corp | |
| FR2201289B1 (enExample) * | 1972-10-02 | 1975-03-14 | Rhone Poulenc Ind | |
| FR2206316B1 (enExample) * | 1972-11-16 | 1976-08-27 | Rhone Poulenc Ind | |
| GB1441704A (en) * | 1973-03-28 | 1976-07-07 | Hitachi Ltd | Thermosetting resin composition |
| US4138406A (en) * | 1973-11-22 | 1979-02-06 | Ciba-Geigy Corporation | Manufacture of maleimides via cyclizing dehydration |
| FR2260567B1 (enExample) | 1974-02-07 | 1976-11-26 | Rhone Poulenc Ind | |
| JPS51117337U (enExample) * | 1975-03-07 | 1976-09-22 | ||
| US4179444A (en) * | 1976-02-11 | 1979-12-18 | Ciba-Geigy Corporation | Process for the manufacture of iso-imides or mixtures of iso-imides and imides |
| CH597184A5 (enExample) * | 1976-04-09 | 1978-03-31 | Ciba Geigy Ag | |
| US4154737A (en) * | 1976-05-05 | 1979-05-15 | E. I. Du Pont De Nemours And Company | Preparation of maleimides and dimaleimides |
| CH634558A5 (de) * | 1978-04-06 | 1983-02-15 | Ciba Geigy Ag | Verfahren zur herstellung von aliphatischen n-substituierten maleinimiden. |
| FR2469421A1 (fr) | 1979-11-09 | 1981-05-22 | Rhone Poulenc Ind | Procede d'encapsulation de composants electroniques a l'aide d'une matiere moulable a base d'un prepolymere thermodurcissable |
| US4351932A (en) * | 1980-03-27 | 1982-09-28 | Hitco | Bis-maleimide/divinyl aryl crosslinking agent resin system |
| US4454283A (en) * | 1981-03-30 | 1984-06-12 | Hitco | Bis-maleimide resin with inhibitor |
| US4468497A (en) * | 1981-03-30 | 1984-08-28 | Hitco | Elastomer modified bis-maleimide resin |
| US4515962A (en) * | 1982-08-05 | 1985-05-07 | Ciba Geigy Corporation | Allyl or methallyl-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid imides and bisimides |
| US4604437A (en) * | 1984-01-31 | 1986-08-05 | Ciba-Geigy Corporation | Polymer from substituted, unsaturated, bicyclic imide |
| DE3604872A1 (de) * | 1986-02-15 | 1987-08-20 | Basf Ag | Verfahren zur herstellung von hitzehaertbaren prepregs aus bismaleinimid-harzen |
| US4808646A (en) * | 1986-12-18 | 1989-02-28 | Monsanto Company | Maleimide-maleamic acid resin solution |
| US4826929A (en) * | 1987-09-24 | 1989-05-02 | Basf Corporation | Toughened bismaleimide resin systems |
| US4945169A (en) * | 1988-07-06 | 1990-07-31 | Indspec Chemical Corporation | Novel bis-maleimide compounds containing sulfonate linkages |
| GB8825790D0 (en) * | 1988-11-03 | 1988-12-07 | Bp Chem Int Ltd | Synthesis of bisimides |
| US5932635A (en) * | 1991-07-30 | 1999-08-03 | Cytec Technology Corp. | Tackified prepreg systems |
| JP3821870B2 (ja) | 1994-10-07 | 2006-09-13 | スリーエム カンパニー | 難燃性熱硬化性樹脂組成物 |
| US5648407A (en) * | 1995-05-16 | 1997-07-15 | Minnesota Mining And Manufacturing Company | Curable resin sols and fiber-reinforced composites derived therefrom |
| JP3085185B2 (ja) * | 1996-03-14 | 2000-09-04 | 日本メクトロン株式会社 | ビスマレイミド化合物およびその製造法 |
| JPH1095898A (ja) * | 1996-09-25 | 1998-04-14 | Sumitomo Bakelite Co Ltd | 難燃性樹脂組成物およびこれを用いた積層板 |
| WO2004096919A1 (ja) * | 1997-04-07 | 2004-11-11 | Masahiro Suzuki | 樹脂組成物及び接着フィルム |
| US5994561A (en) * | 1998-07-28 | 1999-11-30 | Rhein Chemie Rheinau Gmbh | Process for the preparation of aromatic maleimides |
| US7018496B1 (en) | 1999-04-26 | 2006-03-28 | 3M Innovative Properties Company | Curable mechanical fasteners |
| US6565969B1 (en) | 1999-10-21 | 2003-05-20 | 3M Innovative Properties Company | Adhesive article |
| CN100575397C (zh) | 2000-08-22 | 2009-12-30 | Cytec技术有限公司 | 在预浸渍制品中用作增韧剂的柔软聚合物部件 |
| US20030221770A1 (en) * | 2002-05-28 | 2003-12-04 | 3M Innovative Properties Company | Segmented curable transfer tapes |
| US7713604B2 (en) * | 2002-06-17 | 2010-05-11 | 3M Innovative Properties Company | Curable adhesive articles having topographical features therein |
| EP1557449A1 (en) * | 2004-01-22 | 2005-07-27 | 3M Innovative Properties Company | Adhesive tape for structural bonding |
| EP1650279B1 (en) * | 2004-10-19 | 2009-05-27 | 3M Innovative Properties Company | Adhesive article having core/sheath structure |
| US20060116492A1 (en) * | 2004-12-01 | 2006-06-01 | 3M Innovative Properties Company | Branched polymer |
| US20060116476A1 (en) * | 2004-12-01 | 2006-06-01 | 3M Innovative Properties Company | Hybrid thermosetting composition |
| EP1710286A1 (en) * | 2005-04-04 | 2006-10-11 | 3M Innovative Properties Company | Reinforcement Pad |
| CA2607652C (en) | 2005-05-09 | 2013-06-18 | Cytec Technology Corp. | Resin-soluble thermoplastic veil for composite materials |
| GB0717507D0 (en) * | 2007-09-07 | 2007-10-17 | Cytec Tech Corp | Composite materials and their use |
| CN102037083B (zh) * | 2008-03-28 | 2014-02-05 | 3M创新有限公司 | 用于粒子表面改性的方法 |
| EP2265669B1 (en) * | 2008-03-28 | 2018-02-21 | 3M Innovative Properties Company | Filled resins and method for making filled resins |
| BRPI0910662A2 (pt) * | 2008-04-25 | 2015-09-29 | 3M Innovative Properties Co | processo para modificação de superfície de partículas |
| US8541485B2 (en) | 2009-05-26 | 2013-09-24 | 3M Innovative Properties Company | Process for making filled resins |
| US20110160341A1 (en) | 2009-12-30 | 2011-06-30 | E. I. Du Pont De Nemours And Company | Composition for fixing wound items |
| US8871853B2 (en) | 2010-02-11 | 2014-10-28 | 3M Innovative Properties Company | Resin system comprising dispersed multimodal surface-modified nanoparticles |
| JP5809241B2 (ja) | 2010-04-20 | 2015-11-10 | スリーエム イノベイティブ プロパティズ カンパニー | ポリマー表面修飾ナノ粒子を含有する感圧接着剤 |
| CA2853461A1 (en) | 2011-10-24 | 2013-05-02 | 3M Innovative Properties Company | Nanosilica containing bismaleimide compositions |
| EP2780413B1 (en) | 2011-11-16 | 2019-09-25 | 3M Innovative Properties Company | Nanosilica containing polycyanate ester resin compositions |
| CN104870543A (zh) | 2012-12-21 | 2015-08-26 | 3M创新有限公司 | 包含粒子流动助剂的组合物 |
| US10131811B2 (en) | 2013-01-25 | 2018-11-20 | Axalta Coating Systems Ip Co., Llc | Composition for fixing wound items |
| PT2978794T (pt) | 2013-03-28 | 2017-07-05 | Evonik Degussa Gmbh | Misturas curáveis com base em xilileno bismaleimida |
| KR102247428B1 (ko) | 2013-08-13 | 2021-05-03 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 비구형 실리카 나노입자를 함유하는 나노복합재, 복합재, 물품, 및 이의 제조 방법 |
| US10011699B2 (en) | 2014-08-29 | 2018-07-03 | 3M Innovative Properties Company | Inductively curable composition |
-
0
- BE BE754723D patent/BE754723A/xx not_active IP Right Cessation
-
1969
- 1969-08-12 FR FR6927717A patent/FR2055969A5/fr not_active Expired
-
1970
- 1970-08-04 NL NL707011517A patent/NL149163B/xx not_active IP Right Cessation
- 1970-08-10 US US00062623A patent/US3839358A/en not_active Expired - Lifetime
- 1970-08-10 JP JP45069340A patent/JPS4940231B1/ja active Pending
- 1970-08-11 CH CH1204370A patent/CH514585A/fr not_active IP Right Cessation
- 1970-08-11 SE SE10968/70A patent/SE368200B/xx unknown
- 1970-08-11 LU LU61500D patent/LU61500A1/xx unknown
- 1970-08-12 DE DE2040094A patent/DE2040094C3/de not_active Expired
- 1970-08-12 AT AT733770A patent/AT294065B/de not_active IP Right Cessation
- 1970-08-12 GB GB38881/70A patent/GB1276446A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2040094A1 (de) | 1971-03-11 |
| JPS4940231B1 (enExample) | 1974-10-31 |
| LU61500A1 (enExample) | 1971-07-15 |
| US3839358A (en) | 1974-10-01 |
| SE368200B (enExample) | 1974-06-24 |
| NL149163B (nl) | 1976-04-15 |
| FR2055969A5 (enExample) | 1971-05-14 |
| BE754723A (fr) | 1971-02-11 |
| AT294065B (de) | 1971-11-10 |
| DE2040094B2 (de) | 1974-05-02 |
| NL7011517A (enExample) | 1971-02-16 |
| CH514585A (fr) | 1971-10-31 |
| GB1276446A (en) | 1972-06-01 |
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