DE2340558C2 - Resolharz - Google Patents
ResolharzInfo
- Publication number
- DE2340558C2 DE2340558C2 DE2340558A DE2340558A DE2340558C2 DE 2340558 C2 DE2340558 C2 DE 2340558C2 DE 2340558 A DE2340558 A DE 2340558A DE 2340558 A DE2340558 A DE 2340558A DE 2340558 C2 DE2340558 C2 DE 2340558C2
- Authority
- DE
- Germany
- Prior art keywords
- formaldehyde
- aqueous
- addition
- cresol
- condensation resin
- 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
- 229920005989 resin Polymers 0.000 title claims description 9
- 239000011347 resin Substances 0.000 title claims description 9
- 229920003987 resole Polymers 0.000 title claims description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 34
- 238000009833 condensation Methods 0.000 claims description 7
- 230000005494 condensation Effects 0.000 claims description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 229930003836 cresol Natural products 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000010626 work up procedure Methods 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
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/20—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with polyhydric phenols
-
- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/24—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with mixtures of two or more phenols which are not covered by only one of the groups C08G8/10 - C08G8/20
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/36—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes condensation products of phenols with aldehydes or ketones
-
- 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
- C08J2361/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
-
- 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
- C08J2361/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
- C08J2361/04—Condensation polymers of aldehydes or ketones with phenols only
-
- 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
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/905—Polyphenylene oxide
Landscapes
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2340558A DE2340558C2 (de) | 1973-04-19 | 1973-08-10 | Resolharz |
| US461216A US3909495A (en) | 1973-04-19 | 1974-04-15 | Resol resins prepared from dihydroxydiisopropylbenzene |
| NL7405122A NL7405122A (OSRAM) | 1973-04-19 | 1974-04-16 | |
| CH533074A CH586241A5 (OSRAM) | 1973-04-19 | 1974-04-17 | |
| IT50432/74A IT1005979B (it) | 1973-04-19 | 1974-04-17 | Procedimento per produrre resine fenol formaldeidiche del tipo resolo |
| AT317774A AT335176B (de) | 1973-04-19 | 1974-04-17 | Verfahren zur herstellung von resolen |
| JP4278974A JPS576442B2 (OSRAM) | 1973-04-19 | 1974-04-18 | |
| BE143335A BE813873A (fr) | 1973-04-19 | 1974-04-18 | Resines resols |
| FR7413797A FR2226421B1 (OSRAM) | 1973-04-19 | 1974-04-19 | |
| ES425502A ES425502A1 (es) | 1973-04-19 | 1974-04-19 | Procedimiento para la obtencion de resoles. |
| GB1725474A GB1431874A (en) | 1973-04-19 | 1974-04-19 | Resol resins |
| AT986675A AT335179B (de) | 1973-04-19 | 1975-12-29 | Farblose, tiefzieh- und sterilisierfahige resite |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732320009 DE2320009C3 (de) | 1973-04-19 | 1973-04-19 | Resolharze |
| DE2340558A DE2340558C2 (de) | 1973-04-19 | 1973-08-10 | Resolharz |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2340558A1 DE2340558A1 (de) | 1975-02-27 |
| DE2340558C2 true DE2340558C2 (de) | 1983-05-19 |
Family
ID=25765015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2340558A Expired DE2340558C2 (de) | 1973-04-19 | 1973-08-10 | Resolharz |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3909495A (OSRAM) |
| JP (1) | JPS576442B2 (OSRAM) |
| AT (1) | AT335176B (OSRAM) |
| BE (1) | BE813873A (OSRAM) |
| CH (1) | CH586241A5 (OSRAM) |
| DE (1) | DE2340558C2 (OSRAM) |
| ES (1) | ES425502A1 (OSRAM) |
| FR (1) | FR2226421B1 (OSRAM) |
| GB (1) | GB1431874A (OSRAM) |
| IT (1) | IT1005979B (OSRAM) |
| NL (1) | NL7405122A (OSRAM) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57143316A (en) * | 1981-03-02 | 1982-09-04 | Sumitomo Chem Co Ltd | Preparation of resorcin-formaldehyde resin |
| US7196156B2 (en) * | 2002-12-13 | 2007-03-27 | Indspec Chemical Corporation | Flexibilized resorcinolic novolak resins and method of making same |
| RU2463315C1 (ru) * | 2011-04-05 | 2012-10-10 | Федеральное государственное бюджетное учреждение науки Институт элементоорганических соединений им. А.Н. Несмеянова Российской академии наук (ИНЭОС РАН) | Фталидсодержащие соолигомеры для получения сшитых фталидсодержащих сополимеров, способ их получения (варианты), фталидсодержащие сшитые сополимеры на их основе в качестве конструкционных полимеров |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE604516A (OSRAM) * | 1960-06-02 | |||
| US3393244A (en) * | 1961-09-25 | 1968-07-16 | Allied Chem | Bis(p-hydroxycumyl)benzene |
| US3422067A (en) * | 1966-01-03 | 1969-01-14 | Allied Chem | Novel phenolic resins employing bis(p-hydroxycumyl benzene) |
| US3758597A (en) * | 1969-10-09 | 1973-09-11 | Bayer Ag | 2-(hydroxyphenyl)-2-(isopropenylphenyl)-propanes, process for their manufacture |
| DE2027986A1 (de) * | 1970-06-06 | 1971-12-16 | Farbenfabriken Bayer AG 5090 Lever kusen | Verfahren zur Herstellung von alpha, alpha Bis (hydroxyphenyl) diisopropylben zolen |
| DE2107915A1 (de) * | 1971-02-19 | 1972-08-31 | Bayer | Kristalline Resole und Resolharze sowie deren Verwendung für farblose, tiefzieh- und sterilisierfähige Resite |
-
1973
- 1973-08-10 DE DE2340558A patent/DE2340558C2/de not_active Expired
-
1974
- 1974-04-15 US US461216A patent/US3909495A/en not_active Expired - Lifetime
- 1974-04-16 NL NL7405122A patent/NL7405122A/xx not_active Application Discontinuation
- 1974-04-17 AT AT317774A patent/AT335176B/de not_active IP Right Cessation
- 1974-04-17 CH CH533074A patent/CH586241A5/xx not_active IP Right Cessation
- 1974-04-17 IT IT50432/74A patent/IT1005979B/it active
- 1974-04-18 JP JP4278974A patent/JPS576442B2/ja not_active Expired
- 1974-04-18 BE BE143335A patent/BE813873A/xx unknown
- 1974-04-19 FR FR7413797A patent/FR2226421B1/fr not_active Expired
- 1974-04-19 GB GB1725474A patent/GB1431874A/en not_active Expired
- 1974-04-19 ES ES425502A patent/ES425502A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS576442B2 (OSRAM) | 1982-02-04 |
| CH586241A5 (OSRAM) | 1977-03-31 |
| IT1005979B (it) | 1976-09-30 |
| AT335176B (de) | 1977-02-25 |
| DE2340558A1 (de) | 1975-02-27 |
| GB1431874A (en) | 1976-04-14 |
| ES425502A1 (es) | 1976-09-01 |
| BE813873A (fr) | 1974-10-18 |
| JPS5010391A (OSRAM) | 1975-02-03 |
| ATA317774A (de) | 1976-06-15 |
| US3909495A (en) | 1975-09-30 |
| FR2226421B1 (OSRAM) | 1978-01-20 |
| FR2226421A1 (OSRAM) | 1974-11-15 |
| NL7405122A (OSRAM) | 1974-10-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AF | Is addition to no. |
Ref country code: DE Ref document number: 2320009 Format of ref document f/p: P |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8340 | Patent of addition ceased/non-payment of fee of main patent |