FI62547C - Vattenbaserad loesning av eteriserat melamin-formaldehydharts med laong haollbarhetstid och laog halt fri formaldehyd foerfarande foer dess framstaellning och dess anvaendning foer impregnering av fiberprodukter - Google Patents
Vattenbaserad loesning av eteriserat melamin-formaldehydharts med laong haollbarhetstid och laog halt fri formaldehyd foerfarande foer dess framstaellning och dess anvaendning foer impregnering av fiberprodukter Download PDFInfo
- Publication number
- FI62547C FI62547C FI761168A FI761168A FI62547C FI 62547 C FI62547 C FI 62547C FI 761168 A FI761168 A FI 761168A FI 761168 A FI761168 A FI 761168A FI 62547 C FI62547 C FI 62547C
- Authority
- FI
- Finland
- Prior art keywords
- melamine
- formaldehyde
- resin
- temperature
- solution
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title claims description 131
- 230000004044 response Effects 0.000 title 1
- 229920000877 Melamine resin Polymers 0.000 claims description 55
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 48
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 37
- 239000000243 solution Substances 0.000 claims description 37
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 36
- 229920005862 polyol Polymers 0.000 claims description 30
- 150000003077 polyols Chemical class 0.000 claims description 29
- 238000009833 condensation Methods 0.000 claims description 24
- 230000005494 condensation Effects 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 23
- 239000011541 reaction mixture Substances 0.000 claims description 20
- 239000007864 aqueous solution Substances 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 15
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 14
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 11
- 229930006000 Sucrose Natural products 0.000 claims description 11
- 239000005720 sucrose Substances 0.000 claims description 11
- 230000035800 maturation Effects 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 230000007423 decrease Effects 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 4
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 claims description 3
- 230000003472 neutralizing effect Effects 0.000 claims description 3
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 claims 2
- 230000020477 pH reduction Effects 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 114
- 239000011347 resin Substances 0.000 description 114
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 42
- 238000006266 etherification reaction Methods 0.000 description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 40
- 238000002360 preparation method Methods 0.000 description 30
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 21
- 239000000853 adhesive Substances 0.000 description 18
- 230000001070 adhesive effect Effects 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 16
- 238000003860 storage Methods 0.000 description 14
- 239000004202 carbamide Substances 0.000 description 13
- 239000003365 glass fiber Substances 0.000 description 13
- 238000006386 neutralization reaction Methods 0.000 description 9
- 239000011152 fibreglass Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 230000005070 ripening Effects 0.000 description 4
- 229930040373 Paraformaldehyde Natural products 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 230000001627 detrimental effect Effects 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920002866 paraformaldehyde Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- -1 tetramethylene melamines Chemical class 0.000 description 3
- 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 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical class NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 238000010411 cooking Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- 230000010198 maturation time Effects 0.000 description 2
- VIJMMQUAJQEELS-UHFFFAOYSA-N n,n-bis(ethenyl)ethenamine Chemical compound C=CN(C=C)C=C VIJMMQUAJQEELS-UHFFFAOYSA-N 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- OFQCQIGMURIECL-UHFFFAOYSA-N 2-[2-(diethylamino)ethyl]-2',6'-dimethylspiro[isoquinoline-4,4'-oxane]-1,3-dione;phosphoric acid Chemical compound OP(O)(O)=O.O=C1N(CCN(CC)CC)C(=O)C2=CC=CC=C2C21CC(C)OC(C)C2 OFQCQIGMURIECL-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- LGJPPMCUGGWHTN-UHFFFAOYSA-N ethane-1,2-diol methanamine Chemical compound C(CO)O.CN LGJPPMCUGGWHTN-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 239000006060 molten glass Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C03C25/34—Condensation polymers of aldehydes, e.g. with phenols, ureas, melamines, amides or amines
-
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/40—Chemically modified polycondensates
- C08G12/42—Chemically modified polycondensates by etherifying
- C08G12/424—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
- C08G12/425—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines
- C08G12/427—Melamine
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
- D06M15/427—Amino-aldehyde resins modified by alkoxylated compounds or alkylene oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Textile Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7513569 | 1975-04-30 | ||
FR7513569A FR2309575A1 (fr) | 1975-04-30 | 1975-04-30 | Solutions aqueuses de resines melamine-formaldehyde etherifiees a longue duree de conservation et a faible teneur en formaldehyde libre |
Publications (3)
Publication Number | Publication Date |
---|---|
FI761168A7 FI761168A7 (enrdf_load_stackoverflow) | 1976-10-31 |
FI62547B FI62547B (fi) | 1982-09-30 |
FI62547C true FI62547C (fi) | 1983-01-10 |
Family
ID=9154670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI761168A FI62547C (fi) | 1975-04-30 | 1976-04-27 | Vattenbaserad loesning av eteriserat melamin-formaldehydharts med laong haollbarhetstid och laog halt fri formaldehyd foerfarande foer dess framstaellning och dess anvaendning foer impregnering av fiberprodukter |
Country Status (28)
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2715020C2 (de) * | 1977-04-04 | 1983-04-28 | Cassella Ag, 6000 Frankfurt | Verfahren zur Herstellung wäßriger Melamin/Harnstoff-Harzlösungen |
NZ206859A (en) * | 1983-02-07 | 1986-09-10 | Enigma Nv | Formaldehyde binder for boards prepared from lignocellulosic materials |
GB2170208B (en) * | 1985-01-29 | 1988-06-22 | Enigma Nv | A formaldehyde binder |
DE19633625A1 (de) * | 1996-08-21 | 1998-02-26 | Basf Ag | Verfahren zur Herstellung von für die Ausrüstung von cellulosehaltigen textilen Materialien geeigneten wäßrigen konzentrierten Lösungen von N-Methylolethern |
CN110042701B (zh) * | 2019-03-29 | 2023-09-15 | 广东福美新材料科技有限公司 | 一种防潮阻燃浸渍纸及其制备方法 |
RU2019134226A (ru) * | 2019-10-25 | 2021-04-26 | Общество с ограниченной ответственностью "Комберри" | Прозрачные гель-полимерные электролиты повышенной проводимости на основе триазиновых сополимеров |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1012319A (en) * | 1962-06-01 | 1965-12-08 | British Industrial Plastics | Water-soluble modified melamine-formaldehyde resins |
DE2005166C3 (de) * | 1970-02-05 | 1975-05-15 | Chemische Fabrik Pfersee Gmbh, 8900 Augsburg | Verfahren zur Herstellung wasserlöslicher, verätherter Methylolmelamine |
GB1317774A (en) * | 1970-06-02 | 1973-05-23 | British Industrial Plastics | Melamine formaldehyde condensation products |
-
1975
- 1975-04-30 FR FR7513569A patent/FR2309575A1/fr active Granted
-
1976
- 1976-04-06 GB GB13897/76A patent/GB1501534A/en not_active Expired
- 1976-04-12 IE IE777/76A patent/IE43271B1/en unknown
- 1976-04-20 DE DE2617232A patent/DE2617232C2/de not_active Expired
- 1976-04-23 SE SE7604717A patent/SE419229B/xx not_active IP Right Cessation
- 1976-04-26 CA CA251,045A patent/CA1091836A/en not_active Expired
- 1976-04-27 TR TR19067A patent/TR19067A/xx unknown
- 1976-04-27 FI FI761168A patent/FI62547C/fi not_active IP Right Cessation
- 1976-04-28 RO RO7685931A patent/RO70306A/ro unknown
- 1976-04-28 NZ NZ180713A patent/NZ180713A/xx unknown
- 1976-04-29 CH CH540376A patent/CH603737A5/xx not_active IP Right Cessation
- 1976-04-29 BE BE166595A patent/BE841304A/xx not_active IP Right Cessation
- 1976-04-29 AU AU13464/76A patent/AU501880B2/en not_active Expired
- 1976-04-29 DD DD7600192595A patent/DD128380A5/xx unknown
- 1976-04-29 YU YU1084/76A patent/YU37352B/xx unknown
- 1976-04-29 AT AT316676A patent/AT344993B/de not_active IP Right Cessation
- 1976-04-29 LU LU74857A patent/LU74857A1/xx unknown
- 1976-04-29 IT IT68046/76A patent/IT1059948B/it active
- 1976-04-29 MX MX000201U patent/MX3319E/es unknown
- 1976-04-29 BR BR2672/76A patent/BR7602672A/pt unknown
- 1976-04-29 ZA ZA762575A patent/ZA762575B/xx unknown
- 1976-04-29 NL NLAANVRAGE7604581,A patent/NL190286C/xx not_active IP Right Cessation
- 1976-04-29 ES ES447465A patent/ES447465A1/es not_active Expired
- 1976-04-29 HU HU76SA2917A patent/HU177034B/hu unknown
- 1976-04-30 CS CS762877A patent/CS191304B2/cs unknown
- 1976-04-30 NO NO761499A patent/NO142444C/no unknown
- 1976-04-30 JP JP51048690A patent/JPS5853648B2/ja not_active Expired
- 1976-04-30 PL PL1976189203A patent/PL105541B1/pl unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2411468B1 (en) | Binder for fibrous materials | |
JP3594624B2 (ja) | メラミン・ホルムアルデヒト重縮合組成物 | |
CA2634327C (en) | Low emission formaldehyde resin and binder for mineral fiber insulation | |
US4183832A (en) | Aqueous solutions of etherified melamine-formaldehyde resins with long shelf life and low free formaldehyde content | |
US4285848A (en) | Wood adhesive from phenol, formaldehyde, melamine and urea | |
FI62547C (fi) | Vattenbaserad loesning av eteriserat melamin-formaldehydharts med laong haollbarhetstid och laog halt fri formaldehyd foerfarande foer dess framstaellning och dess anvaendning foer impregnering av fiberprodukter | |
PL167251B1 (pl) | Sposób wytwarzania zywicy fenolowej PL PL PL PL | |
SK136095A3 (en) | Soaking resin for foils and borders | |
EP1930361A1 (en) | Random copolymer of oxazoline | |
US3830783A (en) | Process for the preparation of resins from urea,formaldehyde,methanol and formic acid using three stages | |
EP1266917B1 (de) | Wasserverdünnbare verätherte Melamin-Formaldehyd-Harze | |
JP2002511506A (ja) | 改良された加工安定性および低い放出傾向を備えた成形用ポリオキシメチレン組成物 | |
JPH02300209A (ja) | 新規のポリビニルアセタールおよびその用途 | |
HU203777B (en) | Process for producing aquous aminoplast resine composition adhesive composition utilizable for claming mineral fibres and process for producing isolating materials | |
RU2142966C1 (ru) | Способ получения карбамидомеламиноформальдегидных смол | |
CA1163632A (en) | Process for the manufacture of partially etherified methylolmelamines | |
EP0778299B1 (fr) | Procédé de préparation de résines thermodurcissables urée-formol dopées à la mélamine et utilisation de ces résines en tant que résines d'imprégnation | |
KR810000140B1 (ko) | 멜라민-포름알데히드 수지의 제조방법 | |
US6174957B1 (en) | Adhesive composition based on novolac | |
JPH02123103A (ja) | ポリビニルブチラール樹脂 | |
RU2169739C1 (ru) | Способ получения карбамидоформальдегидных смол | |
JPS5830410B2 (ja) | アルコ−ルヘンセイニヨウソジユシセンイ | |
RU2139381C1 (ru) | Состав для изготовления пленочных материалов на основе бумаг | |
JP3035121B2 (ja) | 強化木用淡色フェノール樹脂の製造方法 | |
JP2000290367A (ja) | 耐熱性尿素樹脂の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM | Patent lapsed | ||
MM | Patent lapsed |
Owner name: SAINT-GOBAIN INDUSTRIES |