JPS595150B2 - ハンノウセイセンリヨウノエキジヨウセンリヨウチヨウセイブツ - Google Patents
ハンノウセイセンリヨウノエキジヨウセンリヨウチヨウセイブツInfo
- Publication number
- JPS595150B2 JPS595150B2 JP50138272A JP13827275A JPS595150B2 JP S595150 B2 JPS595150 B2 JP S595150B2 JP 50138272 A JP50138272 A JP 50138272A JP 13827275 A JP13827275 A JP 13827275A JP S595150 B2 JPS595150 B2 JP S595150B2
- Authority
- JP
- Japan
- Prior art keywords
- dye
- weight
- dyes
- parts
- solution
- 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.)
- Expired
Links
- 239000000975 dye Substances 0.000 claims description 130
- 238000002360 preparation method Methods 0.000 claims description 24
- 239000007788 liquid Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 2
- 239000012928 buffer substance Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 33
- 238000004043 dyeing Methods 0.000 description 25
- 239000000843 powder Substances 0.000 description 18
- 239000000985 reactive dye Substances 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 13
- 230000015572 biosynthetic process Effects 0.000 description 11
- 150000003839 salts Chemical class 0.000 description 11
- 238000003786 synthesis reaction Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 238000007796 conventional method Methods 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- -1 β-hydroxyethylsulfonyl group Chemical group 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000001694 spray drying Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 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 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 229910021538 borax Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 235000010339 sodium tetraborate Nutrition 0.000 description 3
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000000872 buffer 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
- 238000001035 drying Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000010014 continuous dyeing Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001599 direct drying Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000004313 glare Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 1
- JMTCDHVHZSGGJA-UHFFFAOYSA-M potassium hydrogenoxalate Chemical class [K+].OC(=O)C([O-])=O JMTCDHVHZSGGJA-UHFFFAOYSA-M 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000002562 thickening agent 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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0072—Preparations with anionic dyes or reactive dyes
- C09B67/0073—Preparations of acid or reactive dyes in liquid form
-
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/503—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
- C09B62/507—Azo dyes
- C09B62/51—Monoazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19742454908 DE2454908C3 (de) | 1974-11-20 | Flüssige Farbstoffzubereitungen von Reaktivfarbstoffen und deren Verwendung |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5173529A JPS5173529A (en) | 1976-06-25 |
JPS595150B2 true JPS595150B2 (ja) | 1984-02-02 |
Family
ID=5931278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP50138272A Expired JPS595150B2 (ja) | 1974-11-20 | 1975-11-19 | ハンノウセイセンリヨウノエキジヨウセンリヨウチヨウセイブツ |
Country Status (13)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0216172U (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1988-07-13 | 1990-02-01 |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4149850A (en) * | 1974-04-09 | 1979-04-17 | Hoechst Aktiengesellschaft | Liquid preparations of reactive dyestuffs |
DE3027546A1 (de) * | 1980-07-21 | 1982-02-18 | Bayer Ag, 5090 Leverkusen | Reaktivfaerbeverfahren |
JPS57105459A (en) * | 1980-12-22 | 1982-06-30 | Sumitomo Chem Co Ltd | Liquid composition of reactive dye |
JPS57153054A (en) * | 1981-03-17 | 1982-09-21 | Sumitomo Chem Co Ltd | Reactive dye composition and method for dyeing by using the same |
DE3126081A1 (de) * | 1981-07-02 | 1983-01-20 | Hoechst Ag, 6000 Frankfurt | Fluessige reaktivfarbstoffzubereitungen und ihre verwendung |
US4448583A (en) * | 1983-02-22 | 1984-05-15 | American Hoechst Corporation | Stable aqueous liquid composition of reactive dyes containing β-sulfatoethylsulfonyl groups |
DE3342432A1 (de) * | 1983-11-24 | 1985-06-05 | Hoechst Ag, 6230 Frankfurt | Fluessige reaktivfarbstoffzubereitungen und ihre verwendung |
DE3413315A1 (de) * | 1984-04-09 | 1985-10-17 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung fluessiger, salzarmer, waessriger reaktivfarbstoffzubereitungen |
DE3426931A1 (de) * | 1984-07-21 | 1986-01-23 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung fluessiger, salzarmer, waessriger reaktivfarbstoffzubereitungen |
JPH0745635B2 (ja) * | 1987-03-26 | 1995-05-17 | 住友化学工業株式会社 | 反応染料の液状水性組成物 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB885547A (en) * | 1959-07-08 | 1961-12-28 | Ici Ltd | New dyestuffs containing triazinylamino and pyrimidylamino radicals |
ZA72558B (en) | 1971-01-30 | 1972-10-25 | Hoechst Ag | Process for dyeing polyamide fibres with reactive dyestuffs |
DE2143750C2 (de) * | 1971-09-01 | 1982-08-05 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung echter Färbungen und Drucke auf hydroxygruppenhaltigem oder stickstoffhaltigem Fasermaterial |
DE2340045B2 (de) * | 1973-08-08 | 1978-02-09 | Hoechst Ag, 6000 Frankfurt | Verfahren zum kontinuierlichen faerben und bedrucken von stueckwaren aus mischungen von synthetischen polyamidfasern mit cellulosefasern mit reaktivfarbstoffen nach der thermofixiermethode |
-
1975
- 1975-01-01 AR AR261248A patent/AR207270A1/es active
- 1975-11-13 CS CS757699A patent/CS187490B2/cs unknown
- 1975-11-17 CH CH1486975A patent/CH576511A5/xx not_active IP Right Cessation
- 1975-11-17 IN IN2195/CAL/75A patent/IN143982B/en unknown
- 1975-11-18 US US05/632,919 patent/US4078884A/en not_active Expired - Lifetime
- 1975-11-18 IT IT29403/75A patent/IT1054400B/it active
- 1975-11-19 JP JP50138272A patent/JPS595150B2/ja not_active Expired
- 1975-11-19 CA CA240,027A patent/CA1061958A/en not_active Expired
- 1975-11-19 BR BR7507665*A patent/BR7507665A/pt unknown
- 1975-11-19 AU AU86749/75A patent/AU497805B2/en not_active Expired
- 1975-11-20 BE BE162046A patent/BE835779A/xx not_active IP Right Cessation
- 1975-11-20 FR FR7535457A patent/FR2292021A1/fr active Granted
- 1975-11-20 GB GB47855/75A patent/GB1512736A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0216172U (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1988-07-13 | 1990-02-01 |
Also Published As
Publication number | Publication date |
---|---|
AR207270A1 (es) | 1976-09-22 |
JPS5173529A (en) | 1976-06-25 |
CS187490B2 (en) | 1979-01-31 |
GB1512736A (en) | 1978-06-01 |
IT1054400B (it) | 1981-11-10 |
DE2454908B2 (de) | 1977-04-28 |
AU497805B2 (en) | 1979-01-11 |
US4078884A (en) | 1978-03-14 |
CH576511A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-06-15 |
FR2292021B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1980-06-27 |
CA1061958A (en) | 1979-09-11 |
IN143982B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-03-04 |
FR2292021A1 (fr) | 1976-06-18 |
DE2454908A1 (de) | 1976-09-23 |
BE835779A (fr) | 1976-05-20 |
BR7507665A (pt) | 1976-08-10 |
AU8674975A (en) | 1977-05-26 |
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