CN103232730B - 一种混拼型分散黄染料 - Google Patents
一种混拼型分散黄染料 Download PDFInfo
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- CN103232730B CN103232730B CN201310010108.4A CN201310010108A CN103232730B CN 103232730 B CN103232730 B CN 103232730B CN 201310010108 A CN201310010108 A CN 201310010108A CN 103232730 B CN103232730 B CN 103232730B
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- Prior art keywords
- dye
- disperse yellow
- chromatid
- mass percent
- compound
- 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.)
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- VGKYEIFFSOPYEW-UHFFFAOYSA-N 2-methyl-4-[(4-phenyldiazenylphenyl)diazenyl]phenol Chemical compound Cc1cc(ccc1O)N=Nc1ccc(cc1)N=Nc1ccccc1 VGKYEIFFSOPYEW-UHFFFAOYSA-N 0.000 title claims abstract description 32
- 239000001043 yellow dye Substances 0.000 title claims abstract description 20
- 150000001875 compounds Chemical class 0.000 title claims abstract description 19
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 239000000126 substance Substances 0.000 claims abstract description 10
- 108091060290 Chromatid Proteins 0.000 claims description 43
- 210000004756 chromatid Anatomy 0.000 claims description 43
- 239000000975 dye Substances 0.000 abstract description 23
- 239000000178 monomer Substances 0.000 abstract description 11
- 238000004043 dyeing Methods 0.000 abstract description 7
- 238000002156 mixing Methods 0.000 abstract description 7
- 239000004576 sand Substances 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000986 disperse dye Substances 0.000 abstract description 2
- 239000012752 auxiliary agent Substances 0.000 description 6
- 239000000835 fiber Substances 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920004933 Terylene® Polymers 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- KTHUKEZOIFYPEH-UHFFFAOYSA-N 1-benzylnaphthalene Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=CC=CC=C1 KTHUKEZOIFYPEH-UHFFFAOYSA-N 0.000 description 1
- WODGMMJHSAKKNF-UHFFFAOYSA-N 2-methylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(C)=CC=C21 WODGMMJHSAKKNF-UHFFFAOYSA-N 0.000 description 1
- RTZYVAQWQXPIAC-UHFFFAOYSA-N 4-[(4-phenyldiazenylphenyl)diazenyl]phenol Chemical compound C1=CC(O)=CC=C1N=NC1=CC=C(N=NC=2C=CC=CC=2)C=C1 RTZYVAQWQXPIAC-UHFFFAOYSA-N 0.000 description 1
- 0 C*c(cc1)ccc1N=N[C@@](C1O)C(*)=NN1C1C=CC=CC1 Chemical compound C*c(cc1)ccc1N=N[C@@](C1O)C(*)=NN1C1C=CC=CC1 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000012932 acetate dye Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
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Abstract
Description
Claims (4)
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CN201310010108.4A CN103232730B (zh) | 2013-01-10 | 2013-01-10 | 一种混拼型分散黄染料 |
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CN201310010108.4A CN103232730B (zh) | 2013-01-10 | 2013-01-10 | 一种混拼型分散黄染料 |
Publications (2)
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CN103232730A CN103232730A (zh) | 2013-08-07 |
CN103232730B true CN103232730B (zh) | 2015-01-14 |
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CN201310010108.4A Active CN103232730B (zh) | 2013-01-10 | 2013-01-10 | 一种混拼型分散黄染料 |
Country Status (1)
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CN (1) | CN103232730B (zh) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN107603273B (zh) * | 2017-09-08 | 2019-05-03 | 浙江龙盛集团股份有限公司 | 一种分散黄染料组合物及其制品 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4062645A (en) * | 1975-05-21 | 1977-12-13 | Montedison S.P.A. | Acid dyes useful for dyeing streaked nylon |
JPH0593044A (ja) * | 1991-08-02 | 1993-04-16 | Sumitomo Chem Co Ltd | 硬化性樹脂組成物 |
CN1125240A (zh) * | 1995-12-20 | 1996-06-26 | 大连理工大学化工学院 | 单偶氮型吡啶酮系复合染料 |
EP0978544A1 (de) * | 1994-02-19 | 2000-02-09 | DyStar Textilfarben GmbH & Co. Deutschland KG | Reaktivfarbstoffmischungen und deren Verwendung zum Färben und Bedrucken von hydroxy- und/oder carbonamidgruppenhaltigen Fasermaterialien |
WO2001017349A1 (en) * | 1999-09-10 | 2001-03-15 | Smithkline Beckman Corporation | Thrombopoietin mimetics |
US6203581B1 (en) * | 1999-11-12 | 2001-03-20 | Everlight Usa, Inc. | Yellow reactive dye composition |
-
2013
- 2013-01-10 CN CN201310010108.4A patent/CN103232730B/zh active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4062645A (en) * | 1975-05-21 | 1977-12-13 | Montedison S.P.A. | Acid dyes useful for dyeing streaked nylon |
JPH0593044A (ja) * | 1991-08-02 | 1993-04-16 | Sumitomo Chem Co Ltd | 硬化性樹脂組成物 |
EP0978544A1 (de) * | 1994-02-19 | 2000-02-09 | DyStar Textilfarben GmbH & Co. Deutschland KG | Reaktivfarbstoffmischungen und deren Verwendung zum Färben und Bedrucken von hydroxy- und/oder carbonamidgruppenhaltigen Fasermaterialien |
CN1125240A (zh) * | 1995-12-20 | 1996-06-26 | 大连理工大学化工学院 | 单偶氮型吡啶酮系复合染料 |
WO2001017349A1 (en) * | 1999-09-10 | 2001-03-15 | Smithkline Beckman Corporation | Thrombopoietin mimetics |
US6203581B1 (en) * | 1999-11-12 | 2001-03-20 | Everlight Usa, Inc. | Yellow reactive dye composition |
Non-Patent Citations (1)
Title |
---|
Synthesis and properties of some novel pyrazolone-based heterocyclic azo disperse dyes containing a fluorosulfonyl group;Ajay Singh,等;《Dyes and Pigments》;20121231;第95卷(第3期);580-586 * |
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CN103232730A (zh) | 2013-08-07 |
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Address after: 318000 three mountain village, Jiaojiang District, Taizhou, Zhejiang Patentee after: Zhejiang Shanyu Group Co.,Ltd. Address before: 318000 three mountain village, Jiaojiang District, Taizhou, Zhejiang Patentee before: ZHEJIANG SHANYU TECHNOLOGY Co.,Ltd. |
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PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A mixed type dispersed yellow dye Effective date of registration: 20231202 Granted publication date: 20150114 Pledgee: Guangfa Bank Co.,Ltd. Taizhou Branch Pledgor: Zhejiang Shanyu Group Co.,Ltd. Registration number: Y2023330002923 |
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