Anthraquinone dyes containing a fluorosulphonyl group and use th

Bleaching and dyeing; fluid treatment and chemical modification – Treatment of hides – skins – feathers and animal tissues – Tanning

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

8532, 8533, 8922, 552242, D06P 326, D06P 354, C09B 6280, C09B 120

Patent

active

057592110

DESCRIPTION:

BRIEF SUMMARY
This application claims benefit of international application PCT/GB95/00097, filed Jan. 23, 1995, published as WO95/21958 Aug. 17, 1995.
The present invention relates to a process for colouring synthetic textile materials, to synthetic textiles when coloured, to a process for the mass coloration of plastics, to plastics when coloured to certain novel anthraquinone dyes and to compositions containing anthraquinone dyes.
According to the present invention there is provided a process for colouring a synthetic textile material or fibre blend thereof which comprises applying to the synthetic textile material a compound of Formula (1): ##STR2## wherein: Ring A and Ring D are optionally substituted and at least one of Ring A or Ring D carries at least one --SO.sub.2 F group sulphonylfluoride, sulphonylfluoride, bisethanesulphonylfluoride, honylfluoride, sulphonylfluoride.
Different compounds of Formula (1) may be mixed or the compounds of Formula (1) may be mixed with dyes which do not contain an --SO.sub.2 F group, such mixtures are a feature of the present invention.
The mixtures may be simple physical mixtures or may be mixed crystals formed for example by co-crystallisation. Such mixtures generally show improvement in dyeing properties. Crystalline modifications of compounds of Formula (1) exist and it is intended that the present definition includes such crystalline modifications which may for example be formed by heat treatment.
According to a further feature of the present invention there is provided a process for colouring a polyester textile material or fibre blend thereof which comprises applying to the polyester textile material sulphonylfluoride, sulphonylfluoride, bisethanesulphonylfluoride, honylfluoride, sulphonylfluoride.
The presence of one or more --SO.sub.2 F groups in a dye molecule generally improves the properties of that dye and confers surprisingly good wet-fastness and light-fastness properties.
The synthetic textile material may be selected from secondary cellulose acetate, cellulose triacetate, polyamide, polyacrylonitrile and aromatic polyester. The synthetic textile material is preferably polyamide or aromatic polyester, such as polyhexamethylene adipamide or polyethylene terephthalate more preferably aromatic polyester and especially polyethlene terephthalate. Fibre blends may comprise mixtures of different synthetic textile materials or mixtures of synthetic and natural textile materials. Preferred fibre blends are those of polyester-cellulose such as polyester-cotton. The textile materials or blends thereof may be in the form of filaments, loose fibres, yarn, woven or knitted fibres.
The dyes of Formula (1) preferably have low solubility in water, typically less than 1% preferably less than 0.5% and especially less than 0.2% solubility in water. The dyes of Formula (1) are thus free from water solubilising groups such as --SO.sub.3 H, --CO.sub.2 H, --PO.sub.3 H and quaternary amino.
The dyes of Formula (1), optionally in conjunction with other disperse dyes may be applied to the synthetic textile materials or fibre blends thereof by methods which are conventionally employed in dyeing disperse dyes to such materials and fibre blends. For example, the dyes of Formula (1) in the form of an aqueous dispersion may be applied by dyeing, padding or printing processes using the conditions and additives conventionally used in carrying out such processes.
The process conditions may be selected from the following: 125.degree. C. to 140.degree. C. for from 10 to 120 minutes and under a pressure of from 1 to 2 bar, a sequestrant may be optionally be added; 190.degree. C. to 225.degree. C. for from 15 seconds to 5 minutes, a migration inhibitor may optionally be added; 160.degree. C. to 185.degree. C. for 4 to 15 minutes for high temperature steaming, or at a temperature of from 190.degree. C. to 225.degree. C. for 15 seconds to 5 minutes for bake fixation with dry heat or at a temperature of from 120.degree. C. to 140.degree. C. and 1 to 2 bar for 10 to 45 minutes for pressure steaming, wetting

REFERENCES:
patent: 2576037 (1951-11-01), Parker et al.
patent: 3952029 (1976-04-01), Krutak, Sr. et al.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Anthraquinone dyes containing a fluorosulphonyl group and use th does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Anthraquinone dyes containing a fluorosulphonyl group and use th, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Anthraquinone dyes containing a fluorosulphonyl group and use th will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-1454160

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.