NL8100793A - Monoazokleurstoffen voor het verven en bedrukken van synthetische vezels. - Google Patents
Monoazokleurstoffen voor het verven en bedrukken van synthetische vezels. Download PDFInfo
- Publication number
- NL8100793A NL8100793A NL8100793A NL8100793A NL8100793A NL 8100793 A NL8100793 A NL 8100793A NL 8100793 A NL8100793 A NL 8100793A NL 8100793 A NL8100793 A NL 8100793A NL 8100793 A NL8100793 A NL 8100793A
- Authority
- NL
- Netherlands
- Prior art keywords
- dyes
- dyeing
- printing
- parts
- dyed
- Prior art date
Links
- 238000004043 dyeing Methods 0.000 title claims description 24
- 238000007639 printing Methods 0.000 title claims description 12
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 title claims description 4
- 229920002994 synthetic fiber Polymers 0.000 title description 3
- 239000012209 synthetic fiber Substances 0.000 title description 3
- 239000000975 dye Substances 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 18
- 239000004744 fabric Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- 229920000728 polyester Polymers 0.000 claims description 12
- 239000004952 Polyamide Substances 0.000 claims description 8
- 229920002647 polyamide Polymers 0.000 claims description 8
- 239000000987 azo dye Substances 0.000 claims description 6
- 229920002301 cellulose acetate Polymers 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims description 3
- 229920006304 triacetate fiber Polymers 0.000 claims description 3
- 239000004753 textile Substances 0.000 claims 3
- 238000010018 discharge printing Methods 0.000 claims 2
- 239000006185 dispersion Substances 0.000 claims 2
- 238000009967 direct dyeing Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 13
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 13
- 235000011150 stannous chloride Nutrition 0.000 description 13
- 239000001119 stannous chloride Substances 0.000 description 13
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- 229920002239 polyacrylonitrile Polymers 0.000 description 3
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 3
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- 241001584775 Tunga penetrans Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 208000016253 exhaustion Diseases 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 238000000859 sublimation Methods 0.000 description 2
- 230000008022 sublimation Effects 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- MHXFWEJMQVIWDH-UHFFFAOYSA-N 1-amino-4-hydroxy-2-phenoxyanthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1 MHXFWEJMQVIWDH-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
- RXQNKKRGJJRMKD-UHFFFAOYSA-N 5-bromo-2-methylaniline Chemical compound CC1=CC=C(Br)C=C1N RXQNKKRGJJRMKD-UHFFFAOYSA-N 0.000 description 1
- VDBJCDWTNCKRTF-UHFFFAOYSA-N 6'-hydroxyspiro[2-benzofuran-3,9'-9ah-xanthene]-1,3'-dione Chemical compound O1C(=O)C2=CC=CC=C2C21C1C=CC(=O)C=C1OC1=CC(O)=CC=C21 VDBJCDWTNCKRTF-UHFFFAOYSA-N 0.000 description 1
- ZYHNHJAMVNINSY-UHFFFAOYSA-N 6-methylsulfonyl-1,3-benzothiazol-2-amine Chemical compound CS(=O)(=O)C1=CC=C2N=C(N)SC2=C1 ZYHNHJAMVNINSY-UHFFFAOYSA-N 0.000 description 1
- 101100534229 Caenorhabditis elegans src-2 gene Proteins 0.000 description 1
- 0 Cc1cc(N(C)C)ccc1N=NC(S)=* Chemical compound Cc1cc(N(C)C)ccc1N=NC(S)=* 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- JSFUMBWFPQSADC-UHFFFAOYSA-N Disperse Blue 1 Chemical compound O=C1C2=C(N)C=CC(N)=C2C(=O)C2=C1C(N)=CC=C2N JSFUMBWFPQSADC-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 238000010017 direct printing Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical class OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000003828 vacuum filtration Methods 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0074—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
- C09B29/0077—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms containing a five-membered heterocyclic ring with one nitrogen and one sulfur as heteroatoms
- C09B29/0085—Thiazoles or condensed thiazoles
- C09B29/0088—Benzothiazoles
-
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
- C09B29/0805—Amino benzenes free of acid groups
- C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
- C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
- C09B29/081—Amino benzenes free of acid groups characterised by the amino group substituted amino group unsubstituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino, aralkylamino or arylamino
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT20069/80A IT1147323B (it) | 1980-02-21 | 1980-02-21 | Monoazocoloranti per la tintura e stampa di fibre sintetiche |
| IT2006980 | 1980-02-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8100793A true NL8100793A (nl) | 1981-09-16 |
Family
ID=11163556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8100793A NL8100793A (nl) | 1980-02-21 | 1981-02-18 | Monoazokleurstoffen voor het verven en bedrukken van synthetische vezels. |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS56139560A (fr) |
| BE (1) | BE887619A (fr) |
| CA (1) | CA1168228A (fr) |
| CH (1) | CH647794A5 (fr) |
| DE (1) | DE3106126A1 (fr) |
| ES (1) | ES499612A0 (fr) |
| FR (1) | FR2476664A1 (fr) |
| GB (1) | GB2070051A (fr) |
| IT (1) | IT1147323B (fr) |
| NL (1) | NL8100793A (fr) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4935676A (fr) * | 1972-08-15 | 1974-04-02 | ||
| JPS6022112B2 (ja) * | 1978-12-25 | 1985-05-31 | 住友化学工業株式会社 | 疎水性繊維を染色または捺染する方法 |
-
1980
- 1980-02-21 IT IT20069/80A patent/IT1147323B/it active
-
1981
- 1981-02-18 NL NL8100793A patent/NL8100793A/nl not_active Application Discontinuation
- 1981-02-19 FR FR8103286A patent/FR2476664A1/fr active Pending
- 1981-02-19 DE DE19813106126 patent/DE3106126A1/de not_active Withdrawn
- 1981-02-19 GB GB8105270A patent/GB2070051A/en not_active Withdrawn
- 1981-02-20 CH CH1138/81A patent/CH647794A5/it not_active IP Right Cessation
- 1981-02-20 ES ES499612A patent/ES499612A0/es active Granted
- 1981-02-20 CA CA000371431A patent/CA1168228A/fr not_active Expired
- 1981-02-20 JP JP2324881A patent/JPS56139560A/ja active Pending
- 1981-02-20 BE BE0/203870A patent/BE887619A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB2070051A (en) | 1981-09-03 |
| ES8300360A1 (es) | 1982-11-01 |
| IT8020069A0 (it) | 1980-02-21 |
| BE887619A (fr) | 1981-08-20 |
| CH647794A5 (it) | 1985-02-15 |
| ES499612A0 (es) | 1982-11-01 |
| DE3106126A1 (de) | 1981-12-24 |
| JPS56139560A (en) | 1981-10-31 |
| IT1147323B (it) | 1986-11-19 |
| FR2476664A1 (fr) | 1981-08-28 |
| CA1168228A (fr) | 1984-05-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BV | The patent application has lapsed |