SU468931A1 - Способ получени модифицированных кетоноформальдегидных смол - Google Patents
Способ получени модифицированных кетоноформальдегидных смолInfo
- Publication number
- SU468931A1 SU468931A1 SU1479669A SU1479669A SU468931A1 SU 468931 A1 SU468931 A1 SU 468931A1 SU 1479669 A SU1479669 A SU 1479669A SU 1479669 A SU1479669 A SU 1479669A SU 468931 A1 SU468931 A1 SU 468931A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dye
- formaldehyde resins
- preparing modified
- formaldehyde
- ketone formaldehyde
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title description 30
- 150000002576 ketones Chemical class 0.000 title description 5
- 229920005989 resin Polymers 0.000 title description 4
- 239000011347 resin Substances 0.000 title description 4
- 238000000034 method Methods 0.000 title description 2
- 239000000975 dye Substances 0.000 description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000000049 pigment Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- -1 cyclohexanop Chemical compound 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical class O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- RCFKEIREOSXLET-UHFFFAOYSA-N disulfamide Chemical compound CC1=CC(Cl)=C(S(N)(=O)=O)C=C1S(N)(=O)=O RCFKEIREOSXLET-UHFFFAOYSA-N 0.000 description 1
- 229950008177 disulfamide Drugs 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD14720570 | 1970-04-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU468931A1 true SU468931A1 (ru) | 1975-04-30 |
Family
ID=5482451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1479669A SU468931A1 (ru) | 1970-04-30 | 1970-09-16 | Способ получени модифицированных кетоноформальдегидных смол |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT304722B (enExample) |
| CH (1) | CH571028A5 (enExample) |
| CS (1) | CS153405B2 (enExample) |
| DE (1) | DE2038410A1 (enExample) |
| FR (1) | FR2060999A5 (enExample) |
| HU (1) | HU164392B (enExample) |
| SU (1) | SU468931A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2613493A1 (de) | 1976-03-30 | 1977-10-06 | Hoechst Ag | Gefaerbte polyester, verfahren zu ihrer herstellung und ihre verwendung zum faerben von kunststoffen |
| GB2305928A (en) * | 1995-10-06 | 1997-04-23 | Coates Brothers Plc | Coloured hot melt ink jet vehicle |
-
1970
- 1970-08-01 DE DE19702038410 patent/DE2038410A1/de active Pending
- 1970-08-19 CH CH1237770A patent/CH571028A5/xx not_active IP Right Cessation
- 1970-08-27 AT AT779870A patent/AT304722B/de not_active IP Right Cessation
- 1970-09-04 FR FR7032302A patent/FR2060999A5/fr not_active Expired
- 1970-09-16 SU SU1479669A patent/SU468931A1/ru active
-
1971
- 1971-04-29 CS CS311171A patent/CS153405B2/cs unknown
- 1971-04-30 HU HUCE000830 patent/HU164392B/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH571028A5 (enExample) | 1975-12-31 |
| CS153405B2 (enExample) | 1974-02-25 |
| DE2038410A1 (de) | 1971-11-11 |
| HU164392B (enExample) | 1974-02-28 |
| AT304722B (de) | 1972-12-15 |
| FR2060999A5 (en) | 1971-06-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HU188164B (en) | Process for colouring thermoplastic and thermosetting polymers, modificated natural resines and linseed oil varnish, and process for producing new 1,4-diketo-pyrrolo /3,4 c/ pyrroles | |
| KR20020007190A (ko) | 미분된 불투명 입자의 제조방법 | |
| SU468931A1 (ru) | Способ получени модифицированных кетоноформальдегидных смол | |
| US2265127A (en) | Pigment composition | |
| DK157303B (da) | Daekkende krystalmodifikation af c.i. pigmentroedt 53:1 i beta-fasen, dens fremstilling og anvendelse | |
| GB770889A (en) | Improvements relating to fluorescent pigments | |
| JPS60161459A (ja) | アジン顔料、その製造方法及びその使用 | |
| TW411359B (en) | Process for the preparation of highly coloured diazo pigment mixtures and solid solutions of diazo pigments | |
| US3316205A (en) | Colored plastic compositions and colors therefor | |
| US4259488A (en) | Bis-isoindoline pigments | |
| US3752686A (en) | Process for the conversion of perylene-3,4,9,10 - tetracarboxylic acid diimide into a form suitable as pigment dyestuff | |
| US3404119A (en) | Polyamides containing a pigment and a basic product obtained from a condensate of napthalene sulphonic acid and formaldehyde | |
| US4028322A (en) | 6-Methylbenzimidazolonylazobarbituric acid pigment | |
| US3137688A (en) | Azo-dyestuffs | |
| DE2361433C2 (de) | Schwer lösliche Disazoverbindungen, ihre Herstellung und Verwendung | |
| DE2739041A1 (de) | Verfahren zum pigmentieren von hochmolekularem organischem material | |
| US3449425A (en) | N,n'-bis(beta-benzophenone)-arylenediamines | |
| DE1928437A1 (de) | Neue Azoverbindungen und Verfahren zu deren Herstellung | |
| DE2420941A1 (de) | Neue monoazopigmente, verfahren zu deren herstellung und verwendung | |
| DE2305071C2 (de) | Wasserunlösliche Disazomethinfarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| JPH0768459B2 (ja) | 染 料 | |
| SU417455A1 (enExample) | ||
| GB487835A (en) | Manufacture of improved pigments | |
| RU1816787C (ru) | N-карбоксиметилимид 4-карбоксиметиламинонафталевой кислоты в качестве люминофора зеленого свечени и способ его получени | |
| JPS63156791A (ja) | 複素環式化合物類、それらの製造方法およびそれらの用途 |