NO772904L - Xylenformaldehydharpikskomposisjoner og fremgangsmaate ved fremstilling av disse - Google Patents
Xylenformaldehydharpikskomposisjoner og fremgangsmaate ved fremstilling av disseInfo
- Publication number
- NO772904L NO772904L NO772904A NO772904A NO772904L NO 772904 L NO772904 L NO 772904L NO 772904 A NO772904 A NO 772904A NO 772904 A NO772904 A NO 772904A NO 772904 L NO772904 L NO 772904L
- Authority
- NO
- Norway
- Prior art keywords
- xylene
- formaldehyde
- acid
- weight
- acidic catalyst
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 14
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 title claims description 12
- 239000008096 xylene Substances 0.000 title claims description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 56
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 claims description 41
- 238000006243 chemical reaction Methods 0.000 claims description 28
- 229920000642 polymer Polymers 0.000 claims description 21
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 229930040373 Paraformaldehyde Natural products 0.000 claims description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 229920002866 paraformaldehyde Polymers 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- UIFVCPMLQXKEEU-UHFFFAOYSA-N 2,3-dimethylbenzaldehyde Chemical compound CC1=CC=CC(C=O)=C1C UIFVCPMLQXKEEU-UHFFFAOYSA-N 0.000 claims description 7
- 239000004793 Polystyrene Substances 0.000 claims description 6
- 239000003377 acid catalyst Substances 0.000 claims description 6
- 229920002223 polystyrene Polymers 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 6
- -1 polyindene Polymers 0.000 claims description 5
- 229920001169 thermoplastic Polymers 0.000 claims description 5
- 239000004416 thermosoftening plastic Substances 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 4
- 229920002319 Poly(methyl acrylate) Polymers 0.000 claims description 2
- 230000009477 glass transition Effects 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 2
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 2
- 239000004800 polyvinyl chloride Substances 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 33
- 239000011347 resin Substances 0.000 description 26
- 229920005989 resin Polymers 0.000 description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- QOJQBWSZHCKOLL-UHFFFAOYSA-N 2,6-dimethylbenzaldehyde Chemical compound CC1=CC=CC(C)=C1C=O QOJQBWSZHCKOLL-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- OIAUFEASXQPCFE-UHFFFAOYSA-N formaldehyde;1,3-xylene Chemical compound O=C.CC1=CC=CC(C)=C1 OIAUFEASXQPCFE-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229940058172 ethylbenzene Drugs 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 150000003738 xylenes Chemical class 0.000 description 2
- ZQHJVIHCDHJVII-OWOJBTEDSA-N (e)-2-chlorobut-2-enedioic acid Chemical compound OC(=O)\C=C(\Cl)C(O)=O ZQHJVIHCDHJVII-OWOJBTEDSA-N 0.000 description 1
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-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
- 229910015900 BF3 Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229940063656 aluminum chloride Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000002991 molded plastic Substances 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000004376 petroleum reforming Methods 0.000 description 1
- 229960004838 phosphoric acid Drugs 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 230000026676 system process Effects 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 238000007039 two-step reaction Methods 0.000 description 1
- 238000000214 vapour pressure osmometry Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G10/00—Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or halogenated aromatic hydrocarbons only
- C08G10/02—Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or halogenated aromatic hydrocarbons only of aldehydes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/18—Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or their halogen derivatives only
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/716,545 US4082728A (en) | 1976-08-23 | 1976-08-23 | Xylene-formaldehyde resin compositions and process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO772904L true NO772904L (no) | 1978-02-24 |
Family
ID=24878434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO772904A NO772904L (no) | 1976-08-23 | 1977-08-22 | Xylenformaldehydharpikskomposisjoner og fremgangsmaate ved fremstilling av disse |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4082728A (it) |
| JP (1) | JPS5326891A (it) |
| AR (1) | AR215645A1 (it) |
| AT (1) | AT356896B (it) |
| AU (1) | AU508354B2 (it) |
| BE (1) | BE857996A (it) |
| BR (1) | BR7705398A (it) |
| CA (1) | CA1114091A (it) |
| CH (1) | CH630650A5 (it) |
| DE (1) | DE2736761A1 (it) |
| DK (1) | DK372277A (it) |
| ES (1) | ES461813A1 (it) |
| FR (1) | FR2362873A1 (it) |
| GB (1) | GB1558640A (it) |
| IT (1) | IT1198302B (it) |
| LU (1) | LU77998A1 (it) |
| MX (1) | MX146732A (it) |
| NL (1) | NL7709044A (it) |
| NO (1) | NO772904L (it) |
| SE (1) | SE7709434L (it) |
| SU (1) | SU755204A3 (it) |
| ZA (1) | ZA774751B (it) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54119595A (en) * | 1978-03-09 | 1979-09-17 | Agency Of Ind Science & Technol | Biodegradable copolymer and its preparation |
| US4176095A (en) * | 1978-07-19 | 1979-11-27 | Standard Oil Company | Reinforced xylene-formaldehyde resin compositions |
| GB2054610B (en) * | 1979-07-07 | 1983-03-09 | Idemitsu Kosan Co | Flame-retardant resin compositions |
| JPH0611780B2 (ja) * | 1985-03-20 | 1994-02-16 | 三菱石油株式会社 | 芳香族メチレン樹脂の製造法 |
| US4689392A (en) * | 1985-04-01 | 1987-08-25 | Mitsubishi Gas Chemical Company, Inc. | Highly reactive aromatic hydrocarbon-formaldehyde resin and process for preparing the same |
| DE3677407D1 (de) * | 1985-04-18 | 1991-03-14 | Mitsubishi Oil Co | Pech fuer die herstellung von kohlenstoffasern. |
| CN113045720B (zh) * | 2019-12-26 | 2022-09-13 | 山东圣泉新材料股份有限公司 | 间二甲苯树脂、其制备方法及绝缘漆 |
| CN111185240B (zh) * | 2020-02-24 | 2022-08-05 | 万华化学集团股份有限公司 | 一种含苯二胺有机多孔聚合物负载型催化剂及制备方法和一种加氢制备间苯二甲胺的方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2597159A (en) * | 1950-04-27 | 1952-05-20 | Pan American Refining Corp | Condensation of aromatic hydrocarbons with formaldehyde catalyzed by formic acid |
| GB942223A (en) * | 1961-07-24 | 1963-11-20 | Exxon Research Engineering Co | Preparation of resins from aromatics and aldehydes |
| GB1015891A (en) * | 1963-08-12 | 1966-01-05 | British Industrial Plastics | Hydrocarbon-formaldehyde resins |
| US3372147A (en) * | 1964-12-21 | 1968-03-05 | Exxon Research Engineering Co | Production of thermosetting aromaticformaldehyde resins |
| DE1570320A1 (de) * | 1965-12-07 | 1970-03-05 | Basf Ag | Verfahren zur Herstellung oelloeslicher Kondensationsprodukte |
| US3723371A (en) * | 1966-04-01 | 1973-03-27 | Sun Oil Co Pennsylvania | Hot melt adhesive having improved creep properties |
| US3378466A (en) * | 1966-06-14 | 1968-04-16 | Exxon Research Engineering Co | Recovery of aromatic formaldehyde resins by steam sparging with an alkali and vacuumdistillation |
| US3700640A (en) * | 1970-12-09 | 1972-10-24 | Exxon Research Engineering Co | Manufacture of aromatic formaldehyde resins |
-
1976
- 1976-08-23 US US05/716,545 patent/US4082728A/en not_active Expired - Lifetime
-
1977
- 1977-08-03 MX MX170098A patent/MX146732A/es unknown
- 1977-08-05 ZA ZA00774751A patent/ZA774751B/xx unknown
- 1977-08-05 CA CA284,169A patent/CA1114091A/en not_active Expired
- 1977-08-10 AU AU27776/77A patent/AU508354B2/en not_active Expired
- 1977-08-12 JP JP9685977A patent/JPS5326891A/ja active Pending
- 1977-08-15 BR BR7705398A patent/BR7705398A/pt unknown
- 1977-08-16 NL NL7709044A patent/NL7709044A/xx not_active Application Discontinuation
- 1977-08-16 AR AR268815A patent/AR215645A1/es active
- 1977-08-16 DE DE19772736761 patent/DE2736761A1/de not_active Withdrawn
- 1977-08-17 FR FR7725095A patent/FR2362873A1/fr active Pending
- 1977-08-18 AT AT598477A patent/AT356896B/de not_active IP Right Cessation
- 1977-08-19 IT IT26820/77A patent/IT1198302B/it active
- 1977-08-19 GB GB34880/77A patent/GB1558640A/en not_active Expired
- 1977-08-22 LU LU77998A patent/LU77998A1/xx unknown
- 1977-08-22 DK DK372277A patent/DK372277A/da not_active Application Discontinuation
- 1977-08-22 SE SE7709434A patent/SE7709434L/xx not_active Application Discontinuation
- 1977-08-22 NO NO772904A patent/NO772904L/no unknown
- 1977-08-22 BE BE180338A patent/BE857996A/xx not_active IP Right Cessation
- 1977-08-22 SU SU772517654A patent/SU755204A3/ru active
- 1977-08-22 ES ES461813A patent/ES461813A1/es not_active Expired
- 1977-08-22 CH CH1028977A patent/CH630650A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB1558640A (en) | 1980-01-09 |
| NL7709044A (nl) | 1978-02-27 |
| AT356896B (de) | 1980-05-27 |
| SE7709434L (sv) | 1978-02-24 |
| ES461813A1 (es) | 1978-05-01 |
| AU2777677A (en) | 1979-02-15 |
| AU508354B2 (en) | 1980-03-20 |
| BR7705398A (pt) | 1978-05-23 |
| ZA774751B (en) | 1978-06-28 |
| DK372277A (da) | 1978-02-24 |
| DE2736761A1 (de) | 1978-03-02 |
| AR215645A1 (es) | 1979-10-31 |
| CH630650A5 (de) | 1982-06-30 |
| MX146732A (es) | 1982-08-04 |
| SU755204A3 (en) | 1980-08-07 |
| IT1198302B (it) | 1988-12-21 |
| JPS5326891A (en) | 1978-03-13 |
| CA1114091A (en) | 1981-12-08 |
| BE857996A (fr) | 1977-12-16 |
| ATA598477A (de) | 1979-10-15 |
| FR2362873A1 (fr) | 1978-03-24 |
| LU77998A1 (fr) | 1979-05-23 |
| US4082728A (en) | 1978-04-04 |
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