SU651708A3 - Способ крашени в массе высокомолекул рного органического материала - Google Patents
Способ крашени в массе высокомолекул рного органического материалаInfo
- Publication number
- SU651708A3 SU651708A3 SU752134152A SU2134152A SU651708A3 SU 651708 A3 SU651708 A3 SU 651708A3 SU 752134152 A SU752134152 A SU 752134152A SU 2134152 A SU2134152 A SU 2134152A SU 651708 A3 SU651708 A3 SU 651708A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- artwork
- dye
- weight
- write
- formula
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 12
- 238000004043 dyeing Methods 0.000 title claims description 6
- 239000011368 organic material Substances 0.000 title claims description 5
- 239000000975 dye Substances 0.000 claims description 18
- 239000000463 material Substances 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 11
- -1 polyethylene terephthalate Polymers 0.000 claims description 9
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 5
- 239000004800 polyvinyl chloride Substances 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 4
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 2
- 239000008187 granular material Substances 0.000 claims 2
- 238000009987 spinning Methods 0.000 claims 2
- 238000000862 absorption spectrum Methods 0.000 claims 1
- 230000008033 biological extinction Effects 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- 239000011105 molded pulp Substances 0.000 claims 1
- 239000002674 ointment Substances 0.000 claims 1
- 235000015927 pasta Nutrition 0.000 claims 1
- 239000004952 Polyamide Substances 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 5
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 229950011260 betanaphthol Drugs 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 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
- UJPSWZBACSJRBS-UHFFFAOYSA-N 4-naphthalen-1-yl-2H-triazin-5-one Chemical class OC=1C(=NN=NC=1)C1=CC=CC2=C1C=CC=C2 UJPSWZBACSJRBS-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000049 pigment Substances 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
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH139866A CH476748A (de) | 1966-02-01 | 1966-02-01 | Verfahren zur Herstellung von Di-(hydroxynaphthyl)-triazinen |
| CH1812666 | 1966-12-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU651708A3 true SU651708A3 (ru) | 1979-03-05 |
Family
ID=25687534
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752134152A SU651708A3 (ru) | 1966-02-01 | 1975-05-12 | Способ крашени в массе высокомолекул рного органического материала |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3478024A (enExample) |
| BE (1) | BE693399A (enExample) |
| CH (1) | CH476748A (enExample) |
| ES (1) | ES336269A1 (enExample) |
| FR (1) | FR1513657A (enExample) |
| GB (1) | GB1107143A (enExample) |
| NL (1) | NL153261B (enExample) |
| SU (1) | SU651708A3 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3632288A (en) * | 1969-05-08 | 1972-01-04 | Foster Grant Co Inc | Process for dyeing styrene polymers |
| US3846422A (en) * | 1972-05-01 | 1974-11-05 | Ciba Geigy Corp | 4,6-bis(alkaryl)-s-triazines |
| US6800757B2 (en) * | 2001-09-27 | 2004-10-05 | Cytec Technology Corp. | Red-shifted triazine ultravioletlight absorbers |
| CN1298775C (zh) * | 2001-10-18 | 2007-02-07 | 西巴特殊化学品控股有限公司 | 作为有机材料稳定剂的萘基三嗪 |
| KR101187002B1 (ko) * | 2003-03-24 | 2012-09-28 | 시바 홀딩 인코포레이티드 | 대칭 트리아진 유도체 |
| PL1888539T3 (pl) * | 2005-06-10 | 2014-03-31 | Basf Se | Hydroksyfenylotriazyny z układem skondensowanych aromatycznych pierścieni karbocyklicznych |
| KR102127963B1 (ko) * | 2007-08-30 | 2020-06-29 | 바스프 에스이 | 미용 조성물의 안정화 |
| JP7147827B2 (ja) * | 2019-12-24 | 2022-10-05 | 東洋インキＳｃホールディングス株式会社 | 紫外線吸収剤、組成物、成形体および積層体 |
| KR20220121794A (ko) * | 2019-12-24 | 2022-09-01 | 토요잉크Sc홀딩스주식회사 | 수지 조성물, 및 성형체 |
| JP7673384B2 (ja) * | 2020-11-13 | 2025-05-09 | ａｒｔｉｅｎｃｅ株式会社 | 樹脂組成物、および成形体 |
| KR20240033216A (ko) | 2021-07-14 | 2024-03-12 | 아티엔스 가부시키가이샤 | 자외선 흡수제 및 그 제조 방법, 조성물, 성형체, 도막 |
| JP7753700B2 (ja) * | 2021-07-15 | 2025-10-15 | ａｒｔｉｅｎｃｅ株式会社 | 組成物、成形体および塗膜 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1566742A (en) * | 1925-12-22 | Heemanjst feitzsche | ||
| US3111518A (en) * | 1960-02-29 | 1963-11-19 | Ciba Ltd | Process for the manufacture of new triazine derivatives and of dyestuffs obtained therefrom |
-
1966
- 1966-02-01 CH CH139866A patent/CH476748A/de not_active IP Right Cessation
-
1967
- 1967-01-25 US US611568A patent/US3478024A/en not_active Expired - Lifetime
- 1967-01-26 FR FR92637A patent/FR1513657A/fr not_active Expired
- 1967-01-27 GB GB4249/67A patent/GB1107143A/en not_active Expired
- 1967-01-31 ES ES336269A patent/ES336269A1/es not_active Expired
- 1967-01-31 NL NL676701494A patent/NL153261B/xx unknown
- 1967-01-31 BE BE693399D patent/BE693399A/xx unknown
-
1975
- 1975-05-12 SU SU752134152A patent/SU651708A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| NL153261B (nl) | 1977-05-16 |
| NL6701494A (enExample) | 1967-08-02 |
| BE693399A (enExample) | 1967-07-03 |
| ES336269A1 (es) | 1968-04-01 |
| CH476748A (de) | 1969-08-15 |
| DE1670423B2 (de) | 1976-01-15 |
| FR1513657A (fr) | 1968-02-16 |
| GB1107143A (en) | 1968-03-20 |
| US3478024A (en) | 1969-11-11 |
| DE1670423A1 (de) | 1971-01-28 |
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