PL94105B2 - - Google Patents

Info

Publication number

PL94105B2

PL94105B2 PL181639A PL18163975A PL94105B2 PL 94105 B2 PL94105 B2 PL 94105B2 PL 181639 A PL181639 A PL 181639A PL 18163975 A PL18163975 A PL 18163975A PL 94105 B2 PL94105 B2 PL 94105B2

Authority

PL

Poland

Prior art keywords

parts

fabric

minutes

weight

subjected

Prior art date

1975-06-27

Links

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• 238000000034 method Methods 0.000 claims description 58
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 45
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 33
• 238000001035 drying Methods 0.000 claims description 32
• 239000000835 fiber Substances 0.000 claims description 15
• 239000000987 azo dye Substances 0.000 claims description 14
• 239000007864 aqueous solution Substances 0.000 claims description 13
• 238000005406 washing Methods 0.000 claims description 13
• 238000010438 heat treatment Methods 0.000 claims description 11
• 229920003043 Cellulose fiber Polymers 0.000 claims description 10
• UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 10
• 238000004043 dyeing Methods 0.000 claims description 10
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
• 150000001875 compounds Chemical class 0.000 claims description 9
• MYKQKWIPLZEVOW-UHFFFAOYSA-N 11h-benzo[a]carbazole Chemical compound C1=CC2=CC=CC=C2C2=C1C1=CC=CC=C1N2 MYKQKWIPLZEVOW-UHFFFAOYSA-N 0.000 claims description 4
• 239000012954 diazonium Substances 0.000 claims description 4
• 150000001989 diazonium salts Chemical class 0.000 claims description 4
• USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 4
• DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 4
• 125000000565 sulfonamide group Chemical group 0.000 claims description 4
• 239000004094 surface-active agent Substances 0.000 claims description 4
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
• DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 claims description 2
• 229940124530 sulfonamide Drugs 0.000 claims description 2
• UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims 2
• MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims 2
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 2
• GDJPWWULUNHAAJ-UHFFFAOYSA-N anthracene-9,10-dione naphthalene Chemical compound C1=CC=CC2=CC=CC=C12.C1=CC=CC=2C(C3=CC=CC=C3C(C12)=O)=O GDJPWWULUNHAAJ-UHFFFAOYSA-N 0.000 claims 1
• 229910000027 potassium carbonate Inorganic materials 0.000 claims 1
• 239000004744 fabric Substances 0.000 description 60
• 229920002678 cellulose Polymers 0.000 description 15
• 239000001913 cellulose Substances 0.000 description 15
• 238000003303 reheating Methods 0.000 description 14
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
• 238000005562 fading Methods 0.000 description 10
• 239000000243 solution Substances 0.000 description 9
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
• 239000004202 carbamide Substances 0.000 description 8
• 239000000203 mixture Substances 0.000 description 7
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
• 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 4
• ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 3
• 230000002378 acidificating effect Effects 0.000 description 3
• 239000012670 alkaline solution Substances 0.000 description 3
• 230000000694 effects Effects 0.000 description 3
• PHQKCVOZVPSTAF-UHFFFAOYSA-N 3-hydroxyanthracene-2-carboxylic acid Chemical compound C1=CC=C2C=C(C=C(C(C(=O)O)=C3)O)C3=CC2=C1 PHQKCVOZVPSTAF-UHFFFAOYSA-N 0.000 description 2
• 239000000975 dye Substances 0.000 description 2
• 239000000376 reactant Substances 0.000 description 2
• 210000002700 urine Anatomy 0.000 description 2
• 230000003313 weakening effect Effects 0.000 description 2
• KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
• MPHSORCNUGSJAA-UHFFFAOYSA-N 2,5-dichlorobenzenediazonium Chemical compound ClC1=CC=C(Cl)C([N+]#N)=C1 MPHSORCNUGSJAA-UHFFFAOYSA-N 0.000 description 1
• SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
• NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
• QCONCWPZAHEPSP-UHFFFAOYSA-N 2-methoxy-4-nitrobenzenediazonium Chemical compound COC1=CC([N+]([O-])=O)=CC=C1[N+]#N QCONCWPZAHEPSP-UHFFFAOYSA-N 0.000 description 1
• -1 2-methyl-5-chlorophenyldiazonium compound Chemical class 0.000 description 1
• MVZMXDJRQFGXSM-UHFFFAOYSA-N 3-hydroxynaphthalene-2,7-disulfonamide Chemical compound C1=C(O)C(S(N)(=O)=O)=CC2=CC(S(=O)(=O)N)=CC=C21 MVZMXDJRQFGXSM-UHFFFAOYSA-N 0.000 description 1
• NJSPBZNGNRRLKD-UHFFFAOYSA-N 6-hydroxynaphthalene-2-sulfonamide Chemical compound C1=C(O)C=CC2=CC(S(=O)(=O)N)=CC=C21 NJSPBZNGNRRLKD-UHFFFAOYSA-N 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
• SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
• 239000000980 acid dye Substances 0.000 description 1
• XLXWAFSNXPPDAB-UHFFFAOYSA-N anthracene;9h-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1.C1=CC=CC2=CC3=CC=CC=C3C=C21 XLXWAFSNXPPDAB-UHFFFAOYSA-N 0.000 description 1
• PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
• 150000004056 anthraquinones Chemical class 0.000 description 1
• 230000003254 anti-foaming effect Effects 0.000 description 1
• 230000002180 anti-stress Effects 0.000 description 1
• 238000010168 coupling process Methods 0.000 description 1
• 239000003431 cross linking reagent Substances 0.000 description 1
• 238000007730 finishing process Methods 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
• 125000005487 naphthalate group Chemical group 0.000 description 1
• 239000003960 organic solvent Substances 0.000 description 1
• 239000000985 reactive dye Substances 0.000 description 1
• 238000007670 refining Methods 0.000 description 1
• 238000002791 soaking Methods 0.000 description 1
• 150000003456 sulfonamides Chemical group 0.000 description 1
• 239000004753 textile Substances 0.000 description 1