SU459893A3 - Способ получени отвержденных полимеров,содержащих свободные и/или этерифицированные метилольные группы - Google Patents
Способ получени отвержденных полимеров,содержащих свободные и/или этерифицированные метилольные группыInfo
- Publication number
- SU459893A3 SU459893A3 SU1746440A SU1746440A SU459893A3 SU 459893 A3 SU459893 A3 SU 459893A3 SU 1746440 A SU1746440 A SU 1746440A SU 1746440 A SU1746440 A SU 1746440A SU 459893 A3 SU459893 A3 SU 459893A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- parts
- polymers containing
- containing free
- methylol groups
- esterified methylol
- Prior art date
Links
- -1 methylol groups Chemical group 0.000 title description 6
- 229920000642 polymer Polymers 0.000 title description 6
- 238000000034 method Methods 0.000 title description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 239000004922 lacquer Substances 0.000 description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-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
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
- UUAGPGQUHZVJBQ-UHFFFAOYSA-N Bisphenol A bis(2-hydroxyethyl)ether Chemical compound C=1C=C(OCCO)C=CC=1C(C)(C)C1=CC=C(OCCO)C=C1 UUAGPGQUHZVJBQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920003270 Cymel® Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- JOVMFYYOLSEUML-UHFFFAOYSA-N butan-1-ol;1,3,5-triazine-2,4,6-triamine Chemical compound CCCCO.NC1=NC(N)=NC(N)=N1 JOVMFYYOLSEUML-UHFFFAOYSA-N 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
- VFGRALUHHHDIQI-UHFFFAOYSA-N butyl 2-hydroxyacetate Chemical compound CCCCOC(=O)CO VFGRALUHHHDIQI-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000021384 green leafy vegetables Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- LDHBWEYLDHLIBQ-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide;hydrate Chemical compound O.[OH-].[O-2].[Fe+3] LDHBWEYLDHLIBQ-UHFFFAOYSA-M 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000001038 titanium pigment Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712107239 DE2107239B2 (de) | 1971-02-16 | 1971-02-16 | Schnell vernetzende einbrennsysteme |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU459893A3 true SU459893A3 (ru) | 1975-02-05 |
Family
ID=5798869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1746440A SU459893A3 (ru) | 1971-02-16 | 1972-02-14 | Способ получени отвержденных полимеров,содержащих свободные и/или этерифицированные метилольные группы |
Country Status (12)
| Country | Link |
|---|---|
| AT (1) | AT312126B (enExample) |
| AU (1) | AU3835472A (enExample) |
| BE (1) | BE779428A (enExample) |
| CA (1) | CA1008585A (enExample) |
| DD (1) | DD96243A5 (enExample) |
| DE (1) | DE2107239B2 (enExample) |
| FR (1) | FR2125962A5 (enExample) |
| GB (1) | GB1361929A (enExample) |
| IT (1) | IT950642B (enExample) |
| NL (1) | NL7202036A (enExample) |
| SU (1) | SU459893A3 (enExample) |
| ZA (1) | ZA72962B (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4163005A (en) * | 1977-08-11 | 1979-07-31 | Velsicol Chemical Corporation | Halobenzene sulfonate flame retardants |
| US4200729A (en) * | 1978-05-22 | 1980-04-29 | King Industries, Inc | Curing amino resins with aromatic sulfonic acid oxa-azacyclopentane adducts |
| DE3166592D1 (en) * | 1980-07-14 | 1984-11-15 | Akzo Nv | Thermosetting coating composition containing a blocked acid catalyst |
| DE3265701D1 (en) * | 1981-02-13 | 1985-10-03 | Ciba Geigy Ag | Curable compositions containing an acid-curable resin, and process for curing them |
| US4504372A (en) * | 1982-03-12 | 1985-03-12 | Ciba-Geigy Corporation | Acid-curable composition containing a masked curing catalyst, and a process for its preparation |
| US4477618A (en) * | 1982-09-29 | 1984-10-16 | Ppg Industries, Inc. | Aminoplast curable coating compositions containing sulfonic acid esters as latent acid catalysts |
| US4469832A (en) * | 1982-09-29 | 1984-09-04 | Ppg Industries, Inc. | Aminoplast curable coating compositions containing polycyclic esters of sulfonic acids as latent acid catalysts |
| US4454274A (en) * | 1982-09-29 | 1984-06-12 | Ppg Industries, Inc. | Aminoplast curable coating compositions containing cycloaliphatic sulfonic acid esters as latent acid catalysts |
| FR2538402B1 (fr) * | 1982-12-24 | 1985-10-25 | Charbonnages Ste Chimique | Procede de durcissement de resines phenoliques |
| US4550137A (en) * | 1983-03-28 | 1985-10-29 | Ppg Industries, Inc. | Lactam derived salts of sulfonic acids as latent acid catalysts |
| US4501854A (en) * | 1983-11-14 | 1985-02-26 | Ppg Industries, Inc. | Aminoplast curable compositions containing disulfonic acid esters as latent acid catalysts |
| US4500680A (en) * | 1983-11-14 | 1985-02-19 | Ppg Industries, Inc. | Aromatic acid catalysts providing improved humidity resistance |
| EP0206588B1 (en) * | 1985-06-04 | 1990-09-12 | Sumitomo Chemical Company, Limited | Copolymer binder composition and fabrics and papers treated therewith |
| WO2009045466A1 (en) | 2007-10-02 | 2009-04-09 | King Industries | Sulfonate esters as latent acid catalysts |
-
1971
- 1971-02-16 DE DE19712107239 patent/DE2107239B2/de not_active Withdrawn
-
1972
- 1972-01-26 AU AU38354/72A patent/AU3835472A/en not_active Expired
- 1972-02-14 IT IT48307/72A patent/IT950642B/it active
- 1972-02-14 SU SU1746440A patent/SU459893A3/ru active
- 1972-02-14 CA CA134,593A patent/CA1008585A/en not_active Expired
- 1972-02-14 AT AT116572A patent/AT312126B/de not_active IP Right Cessation
- 1972-02-15 DD DD160884A patent/DD96243A5/xx unknown
- 1972-02-15 GB GB696072A patent/GB1361929A/en not_active Expired
- 1972-02-15 ZA ZA720962A patent/ZA72962B/xx unknown
- 1972-02-16 BE BE779428A patent/BE779428A/xx unknown
- 1972-02-16 NL NL7202036A patent/NL7202036A/xx unknown
- 1972-02-16 FR FR7205240A patent/FR2125962A5/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL7202036A (enExample) | 1972-08-18 |
| FR2125962A5 (enExample) | 1972-09-29 |
| GB1361929A (en) | 1974-07-30 |
| ZA72962B (en) | 1973-08-29 |
| DE2107239A1 (de) | 1972-09-07 |
| IT950642B (it) | 1973-06-20 |
| CA1008585A (en) | 1977-04-12 |
| AU3835472A (en) | 1973-08-02 |
| AT312126B (de) | 1973-12-27 |
| DE2107239B2 (de) | 1977-09-22 |
| DD96243A5 (enExample) | 1973-03-12 |
| BE779428A (fr) | 1972-08-16 |
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