US1667524A - Process for dyeing artificial silk - Google Patents

Process for dyeing artificial silk Download PDF

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Publication number
US1667524A
US1667524A US180610A US18061027A US1667524A US 1667524 A US1667524 A US 1667524A US 180610 A US180610 A US 180610A US 18061027 A US18061027 A US 18061027A US 1667524 A US1667524 A US 1667524A
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US
United States
Prior art keywords
acid
dyeing
artificial silk
amino
combining
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 - Lifetime
Application number
US180610A
Inventor
Baddiley James
Chorley Percy
Butler Carlton
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
British Dyestuffs Corp Ltd
Priority date (The priority date 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 date listed.)
Filing date
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Application filed by British Dyestuffs Corp Ltd filed Critical British Dyestuffs Corp Ltd
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Publication of US1667524A publication Critical patent/US1667524A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/02Disazo dyes
    • C09B31/025Disazo dyes containing acid groups, e.g. -COOH, -SO3H, -PO3H2, -OSO3H, -OPO2H2; Salts thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/916Natural fiber dyeing
    • Y10S8/918Cellulose textile

Definitions

  • the said components are 1-: 8-dihydro'xy naphthalene sulphonie acids, 1:8-amino naphthol-sulphonic acids and N-substituted derivatives of the latter.
  • Secondary disazo v compounds are thoseobtained by the action ofia diazoazo compound on an amine or a phenol.
  • the dyestuffs have a good afiinity for regenerated cellulose silks and possess thevaluable property of giving level dyeings' on these fibres.
  • the regenerated cellulose silk fibres have hitherto given considerable diiiiculty in dyeing owing to the fact that they are liable to possess an uneven aflinity for dyestufi's, which causes the dyeings obtained to be unlevel. This difliculty is encountered particularly when it is desired to' dye the fibre in blue and green shades. The shades which we obtain are blue, reen and black and are very level, and our iscovery is therefore of v considerable technical value.
  • ' 40 or its 1: 2:3 isomer, or the technical mixture of these two isomers, and the homologues of any of these may be used.
  • middle components there may be used anaphthylamine, l-amino-Q-naphthol others.
  • a dyebath is made up from 3000 parts of water, 20 parts of Glaubers salt, 2 'parts of soap and one part of the secondary disazo dye obtained by combining 5-aminosalic lie acid with I-amino-Q-naphthol ethyl et er,
  • naphthoi-3z6-disulg gonic acid Ditto Cloves acid 1: ihydroxynaph- Groenish.
  • sotinic acid amine. thalehedzmiii- 0 mi am i ii ir n o b -a no-p-cre- 0..-. or a i sotinic acid. twain-3:04a ii]- my u.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

Patented Apr. 24, 1928.
. UNITED STATES, PATENT OFFICE.
1mm nanmnnr, PERCY CHOBLEY, Ann cnnn'ron nu'rnnn, or mucnns'rnn, Enenann assrenons. ro :emrrsn n n s'rorrs conrona'rron Lmnnn, or m. cnns'rnn, nnemn, a company 02- GREAT nnnram AND mum).
raocnss non nYnme ARTIFICIAL srnx No Drawing. Application flied April '2, 1927, Serial No. 180,610, and in Great Britain June 4, 19M.
Accordin to this invention, regenerated- .10 naphthalene derivatives asend components.
The said components are 1-: 8-dihydro'xy naphthalene sulphonie acids, 1:8-amino naphthol-sulphonic acids and N-substituted derivatives of the latter. Secondary disazo v compounds are thoseobtained by the action ofia diazoazo compound on an amine or a phenol. The use oi dyestuffs of the present type for dyeing chrome mordanted wool and for chrome printinghaslon been known,
but we'havenow' made the entlrely unexpected discovery that the dyestuffs have a good afiinity for regenerated cellulose silks and possess thevaluable property of giving level dyeings' on these fibres.
The regenerated cellulose silk fibres have hitherto given considerable diiiiculty in dyeing owing to the fact that they are liable to possess an uneven aflinity for dyestufi's, which causes the dyeings obtained to be unlevel. This difliculty is encountered particularly when it is desired to' dye the fibre in blue and green shades. The shades which we obtain are blue, reen and black and are very level, and our iscovery is therefore of v considerable technical value.
The aminosalicyhc aclds we use may be either 5-aminosalicylic acid (COOH; OH: NH .=1:2: 5)
' 40 or its 1: 2:3 isomer, or the technical mixture of these two isomers, and the homologues of any of these may be used. As middle components, there may be used anaphthylamine, l-amino-Q-naphthol others.
l-naphthylamine-G- or 7-sulphonic acids, 1-
A dyebath is made up from 3000 parts of water, 20 parts of Glaubers salt, 2 'parts of soap and one part of the secondary disazo dye obtained by combining 5-aminosalic lie acid with I-amino-Q-naphthol ethyl et er,
rediazotizing and combining with 1:8-dihydroxynaphthalene 4 sulphonic acid. 100 parts of the regenerated cellulose silk are entered into the bath at about 30'. C., the bath is then heated to about C. and dyemg allowed to proceed for about one hour. The silk is then removed, rinsed and dried. The resulting dyeing is a level bright green shade.
The following table contains other examples of the shades which can be obtained by our invention Secondary disuo dies from-- shadeal l First eorn- Middle component pone, End component flaminosaiicyiic a-naphthyi- 1:8-aminonaphthoi- 'Groeniahacid. I amine. 3:6-disulphonie black.
mm .-ditto. 1:8-diliydtox a a- B! b thalene-3zfia in ilu.- not phonic acid. Ditto ditto.. 1:8-aminonaphthoi- Blue-black.
2:4 3iisuiphonic sci Aminosaiicyiic m-amino-p- 1:8-dihydroxyna h- Blue.
acid. Tech- I cresoi. thaienwsuipiionnical mixture. ic acid. Aminosaiicyiic n-naphthyl- 1:8-dihydroxyna h- Blue.
acid. Techamine. thalene-t-suip onnicai mixture ic acid.
itto ...ditto.... l-wetyiamino-8- Blue-black.
naphthoi-3z6-disulg gonic acid. Ditto Cloves acid 1: ihydroxynaph- Groenish.
(mixed). lthaiuge-i-suiphonblue. cac p-amino-ocrea-naphthyl- 1:8-dih drox h- Biue.
sotinic acid. amine. thalehedzmiii- 0 mi am i ii iir n o b -a no-p-cre- 0..-. or a i sotinic acid. twain-3:04a ii]- my u.
, phonic acid.
. What we claim and desire to secure by Letters Patent is 1.The process of dyeing which com rises dyeing regenerated cellulose silks wit the secondary disazo dyestuifs which can be made by combining amino-oydroxg carbox acids of the benzene series witht e usual iddle components, further diazomade by combining amino-o-hydrox carboxy acids of the benzene series with t e usual middle components further diazotizing and combining with a sulphonated 5 1:8-dihydroxynaphthalene.
3. The process of dyeing which comprises dyeing regenerated cellulose silks with the secon ary disazo dyestufis which can be made by combining amino-o-hydroxy- 10 carboxy acids of the benzene series with the usual middle components, further diazotizing and combining with a ,1 B-dihydroxynaphthalene-et-sul honic acid.
4. As new in ustrial products, regenerated cellulose silks dyed by the process of claim 1.
In, testimony whereof we aflix our signatures. y
' JAMES BADDILEY. I PERCY CHORLEY.
CARLTON BUTLER.
US180610A 1926-06-04 1927-04-02 Process for dyeing artificial silk Expired - Lifetime US1667524A (en)

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GB1667524X 1926-06-04

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