A dye scavenger.
Abstract
A process for preventing discoloration of a textile material comprising washing one or more dyed textile materials (herein defined as "the wash") that contain free dye or liberatable dye (i.e dye that can be washed out of the material) in the presence of a dye scavenger (for taking up any free dye or any dye that is liberated in the wash) the scavenger comprising a substrate to which a polymeric material (hereinafter referred to as the polymeric material) selected from any one of Products A to D is applied, where Products A to D, are as follows: (A) a polymeric reaction product of a monofunctional or polyfunctional amine having one or more primary and/or secondary tertiary amino groups with cyanamide , dicyandiamide (DCDA), guanidine or bisguanide where up to 50% of cyanamide, dicyandiamide, guanidine or bisguanide may be replaced by a dicarboxylic acid or a mono- or di-ester thereof, said product (A) containing at least one free hydrogen atom linked to a nitrogen atom (hereinafter referred to as Product A); or(B) a water soluble polymeric reaction product of (A) with an epihalohydrin or a precursor thereof,(hereinafter referred to as Product B); or(C) a water soluble homopolymer of a mono- or di-allyl amine, or a copolymer of mono-and di-allylamine, in which at least one N atom is capable of forming an acid addition salt and/or at least one N atom is an ammonium group (hereinafter referred to as Product C); or(D) a water soluble copolymer, of a mono- and/or di- and/or triallylamine with a copolymerisable monomer, in which at least one N atom is capable of forming an acid addition salt and/or at least one N atom is a quaternary ammonium group (hereinafter referred to as Product D); or a mixture of one or more of Products A to D.
Term
Term ended
Projected expiry passed 25 April 2009, 17.4 years ago.
- Priority
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- Published
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- Today
10 claims: 6 independent, 4 dependent
- 1A process for reducing or preventing discoloration of a textile material in a wash bath comprising washing one or more dyed textile materials (herein defined as "the wash") that contain free dye or liberatable dye (i.e dye that can be washed out of the material) together with a textile material that can be discolored in the presence of a dye scavenger (for taking up any free dye or any dye that is liberated in the wash) the scavenger comprising a substrate to which a polymeric material (hereinafter referred to as the polymeric material) selected from any one of Products A to D, is applied where Products A to D are as follows:(A) a polymeric reaction product of a monofunctional or polyfunctional amine having one or more primary and/or secondary tertiary amino groups with cyanamide , dicyandiamide (DCDA), guanidine or bisguanide where up to 50% of cyanamide, dicyandiamide, guanidine or bisguanide may be replaced by a dicarboxylic acid or a mono- or di-ester thereof, said product (A) containing at least one free hydrogen atom linked to a nitrogen atom (hereinafter referred to as Product A);or (B) a water soluble polymeric reaction product of (A) with an epihalohydrin or a precursor thereof,(hereinafter referred to as Product B);or (C) a water soluble homopolymer of a mono- or di-allyl amine, or a copolymer of mono-and di-allylamine, in which at least one N atom is capable of forming an acid addition salt and/or at least one N atom is an ammonium group (hereinafter referred to as Product C);or (D) a water soluble copolymer, of a mono- and/or di- and/or triallylamine with a copolymerisable monomer in which at least one N atom is capable of forming an acid addition salt and/or at least one N atom is a quaternary ammonium group (hereinafter referred to as Product D);or a mixture of one or more of Products A to D.
- 2A process according to Claim 1 in which the dye scavenger is undyed.
- 4A process according to any one of the preceding claims in which the polymeric material is Product A.
- 5A process according to any one of the preceding claims in which the polymeric product is the reaction product of diethylene triamine or triethylene tetraamine with DCDA reacted at an elevated temperature in the presence of a catalyst selected from metals, metal salts and heterocyclic nitrogen - containing organic bases.
- 6A process according to Claim 5 in which the catalyst is zinc chloride.
- 7A process according to any one of the preceding claims in which the polymeric material is a synergistic mixture containing as active ingredient a textile auxiliary (T) and the polymeric compound (P) in which T is the product of a 2-step reaction comprising the steps of 1) reacting an epihalohydrin with aqueous ammonia at 50-90°C in an initial mole ratio of 4 moles epihalohydrin to 8 to 10 moles of ammonia and 2) reacting the product of step 1, after removal of excess ammonia, with a further 0.1 to 0.5 moles of epihalohydrin and P is a water soluble homopolymer of a mono-or di-allylamine, or a water soluble copolymer comprising mono-, di- or tri-allylamine units.
- 8A process according to Claim 7 in which the polymeric material also contains 3) the reaction product of epichlorohydrin or a precursor thereof with polyalkylene polyamine.
- 9A process substantially as herein defined with reference to any one of the Examples.
- 10The use of a scavenger defined in any one of the preceding claims for reducing or preventing discoloration of a textile material in a wash bath.
Independent claims10
41 paragraphs, as filed
0001One problem that arises with dyed material that contains either free dye or dye that is not sufficiently well bound to the material is that it is not retained in the material during a conventional household washing procedure, that is to say the free or insufficiently well bound dye is liberated and can therefore be taken up by other substrates, (which may be dyed or undyed) thereby affecting the colour or indeed causing colouring of these other substrates.
0002To alleviate this problem, there is provided according to the invention, a process for reducing or preventing discoloration of a textile material in a wash bath, comprising
0003washing one or more dyed textile materials (herein defined as "the wash") that contain free dye or liberatable dye (i.e dye that can be washed out of the material) in the presence of a dye scavenger capable of taking up any free dye or any dye that is liberated in the wash, the scavenger comprising a substrate to which a polymeric material, (hereinafter referred to as the polymeric material) selected from any one of Products A to D, is fixed where Products A to D are as follows: <ul id="ul0001" list-style="none"><li>(A) a polymeric reaction product of a monofunctional or polyfunctional amine having one or more primary and/or secondary tertiary amino groups with cyanamide , dicyandiamide (DCDA), guanidine or bisguanide where up to 50% of cyanamide, dicyandiamide, guanidine or bisguanide may be replaced by a dicarboxylic acid or a mono- or di-ester thereof, said product (A) containing at least one free hydrogen atom linked to a nitrogen atom (hereinafter referred to as Product A); or</li><li>(B) a water soluble polymeric reaction product of (A) with an epihalohydrin or a precursor thereof, (hereinafter referred to as Product B); or</li><li>(C) a water soluble homopolymer of a mono- or di-allyl amine, or a copolymer of mono-and di-allylamine, in which at least one N atom is capable of forming an acid addition salt and/or at least one N atom is an ammonium group (hereinafter referred to as Product C); or</li><li>(D) a water soluble copolymer, of a mono- and/or di- and/or triallylamine with a copolymerisable monomer ,in which at least one N atom is capable of forming an acid addition salt and/or at least one N atom is a quaternary ammonium group (hereinafter referred to as Product D);</li></ul> or a mixture of one or more of Products A to D.
0004The dye scavenger may be dyed or undyed. Preferably the scavenger is undyed.
0005Preferably the polymeric material of the dye scavenger has a molecular weight of over 4000, more preferably over 5000.
0006Product A is known, and is described for example in British Published Patent Application No 2 142 642, US Patent 4 764 585 and US Patent 4 410 652, and may be prepared by methods described in said patents,the contents of which are incorporated herein by reference.
0007Suitably the amine, in free base or salt form, is reacted with the other starting material in the absence of water at elevated temperatures optionally in the presence of a non-aqueous solvent. Preferably the reaction is carried out in the absence of solvent at a temperature of 140-160°C, and for most combinations of reagents, ammonia is evolved. The reagents are preferably reacted in a molar ratio of 0.1 to 1 mole of cyanamide, DCDA, guanidine or biguanide per mole of reactive -NH- or -NH₂ group, and when DCDA is reacted with a polyalkylene polyamine, the molar ratio of the reactants is more preferably from 2:1 to 1:2, particularly about 1:1. Preferably the reactants are reacted in the presence of a catalyst selected from metals, metal salts and heterocyclic nitrogen-containing compounds (defined as catalyst K in USP 4 764 585).
0008The Products A are near-colourless viscous liquids or solids which are basic in character, water-soluble either in the free base or salt form, and contain reative hydrogen atoms bonded to nitrogen.
0009Up to 50 mole % preferably up to 20 mole % of the DCDA or other reagent to be reacted with the amine may be replaced by a dicarboxylic acid or a mono- or di-ester thereof. Suitable acids include adipic acid, oxalic acid and terephthalic acid, for example in the form of their dimethyl esters.
0010Particularly preferred Products A are the reaction products of DCDA with diethylenetriamine or triethylenetetramine, preferably in the presence of a catalyst selected from metals, metal salts and heterocyclic nitrogen containing compounds (especially zinc chloride) defined as catalyst K in USP 4 764 585.
0011Product B is described in USP 4,439,203 the contents of which are incorporated herein by reference.
0012Products C and D are described in Japanese Kokai:- 51-57 793 ; 56-9999 ; 56-53 292 ; 56-134 284 ; 57-11 288 ; 57-591 ; 57-92 012 ; 60-7079 ; 45-1457 and 49-31 631 ; the contents of which are incorporated herein by reference.
0013Further products of Product C and D are described in EP 280,655, the contents of which are incorporated herein by reference as well as D.O.S. 37 205 08.
0014Preferably the polymeric material is Product A, C, or D.
0015More preferably the polymeric material of the scavenger is Product A or Product C′; where Product C′ is a synergistic mixture containing as active ingredient a textile auxiliary (T) and the polymeric compound (P) in which T is the product of a 2-step reaction comprising the steps of <ul id="ul0002" list-style="none"><li>1) reacting an epihalohydrin with aqueous ammonia at 50-90°C in an initial mole ratio of 4 moles epihalohydrin to 8 to 10 moles of ammonia and</li><li>2) reacting the product of step 1, after removal of excess ammonia, with a further 0.1 to 0.5 moles of epihalohydrin; and</li></ul>
0016P is a water soluble homopolymer of a mono-or di-allylamine, or a water soluble copolymer comprising (preferably consisting of) mono-, di- or tri-allylamine units.
0017Such a product is described in EP 280,655 (= US Serial No. 07/151,032)
0018The synergistic mixture may also contain 3) the reaction product of epichlorohydrin or a precursor thereof with a polyalkylene polyamine.
0019Most preferably the polymeric Product is Product A (especially Product of Example 1 as described in USP 4 764 585).
0020The amount of polymeric material to substrate of scavenger is to 20 %, more preferably 2 to 6 %, by weight of substrate.
0021The scavenger can be in any form. The polymeric material can be applied to the whole substrate or to just a surface. Preferred substrates including fabrics, garments, films, non-woven material or paper.
0022The substrates can be natural or synthetic, preferably undyed cotton, undyed regenerated cellulose or undyed natural or synthetic polyamide.
0023The substrates can be treated with any one of Products A to D by known methods, for example by immersion, padding, spraying, printing, exhaustion. The amount used is preferably from 2 to 200 g/l, more preferably 10 to 80 g/l (based on the activates of components A to D) preferably in a goods to liquor ratio of 1:1 to 1:30.
0024The scavenger that is so produced can be used in standard washing procedures, merely by being added to the wash. The scavenger takes up any free or liberated dyestuff, in particular anionic dyestuff, free in the bath. In this way, the scavenger assists in preventing staining of the washing by free dye being taken up undesirably on other pieces in the wash. The scavenger is optimally effective with dyeings, preferably of not more than 1/1 standard depth, especially in light shades.
0025The amount of scavenger should be sufficient to prevent as reduce staining and/or discoloration. This amount will vary depending on the total amount of wash and also on the properties of wash that contains free or liberatable dye.
0026The amount of scavenger to the wash is preferably 5 to 80 g to 1 kg of the wash; more preferably 10 to 30 g to 1 kg of wash.
0027Preferably the substrate of scavenger is a textile material.
0028In this specification, unless indicated to the contrary reference to Products A to D includes reference to mixtures thereof.
0029The invention will now be illustrated by the following Examples in which all parts of percentages are by weight and all temperatures are in °C unless indicated to the contrary.
Example 1.
0030A fabric of 100 % cotton is impregnated by padding (squeezed to 80 % dry weight) with 60 g/l of the product of Example 1 of US Patent 4,764,585 (= D.O.S 35,25,104) - calculated on 100 % active substance- and this is dried at 100°C. The textile material (hereinafter referred to as the "scavenger") is then added to a household coloured wash made up of cotton textile fabric dyed with C.I. Reactive Violet 23 and undyed cotton textile fabric. The weight of the wash is 3 kg and the wash to bath ratio is 1:4. The washing powder used was "0mo", a commercially available product, for a 60°C wash and was used in an amount of 6 g/l.
0031The amount (by weight) of scavenger to washing is about 1 that is to say 30 g of scavenger is used.
0032The wash and scavenger is then washed in a Bauknecht washing machine, a commercially available household machine, at 60 °C and is then dried.
0033After drying it can be seen that the dye scavenger has taken up dye from the insufficiently fast dyeing.
Example 2
0034Example 1 is repeated, using instead of the C.I. Reactive Violet 23, C.I. Direct Blue 251. The resulting scavenger is soiled with free dye.
Example 3
0035A dye scavenger is prepared using the polymeric product of Example 1 of GB 2,192,893 A (= D.O.S. 3′720′508)
0036Example 1 is repeated using the following wash. 60-70 % cotton dyed with C.I. Direct Blue 251 ; 10 % nylon dyed with the dye of Example 1 of D.O.S. 2,400,654 ; 15 % Dacron T56, dyed with C.I. Disperse Yellow 23 ; and 5 % Orlon dyed with C.I. Basic Blue 45.
0037The wash is then washed with the scavenger at 60°C. The scavenger picks up the free dye available (primarily of C.I. Direct Blue 251) whereas the fabrics of the wash retain their clear colours.
0038In all the Examples there is substantially no or very little soiling of the other fabrics of the wash than the scavenger by free or liberated dye.
Every citation, both ways
| Document | Relation | Office | Category | Cited during |
|---|---|---|---|---|
| US6255271B1 | Cited by | United States of America | – | Applicant |
| US5843192A | Cited by | United States of America | – | Search report |
| EP1239025A2 | Cited by | European Patent Office (EPO) | – | Search report |
| US7544652B2 | Cited by | United States of America | – | Applicant |
| EP1236793A2 | Cited by | European Patent Office (EPO) | – | Search report |
| US7091167B2 | Cited by | United States of America | – | Applicant |
| US6180593B1 | Cited by | United States of America | – | Applicant |
| US6858570B2 | Cited by | United States of America | – | Applicant |
| EP1239025A3 | Cited by | European Patent Office (EPO) | – | Search report |
| WO2006027203A1 | Cited by | World Intellectual Property Organization (WIPO) | – | International search |
| US5730760A | Cited by | United States of America | – | Search report |
| US7256166B2 | Cited by | United States of America | – | Applicant |
| US5380447A | Cited by | United States of America | – | Search report |
| US6277810B2 | Cited by | United States of America | – | Applicant |
| EP1236793A3 | Cited by | European Patent Office (EPO) | – | Search report |
| US6887524B2 | Cited by | United States of America | – | Applicant |
| US6833336B2 | Cited by | United States of America | – | Applicant |
| US6830593B1 | Cited by | United States of America | – | Applicant |
| US7585831B2 | Cited by | United States of America | – | Applicant |
| US7541326B2 | Cited by | United States of America | – | Applicant |
| US5534182A | Cited by | United States of America | – | Search report |
| WO0015755A1 | Cited by | World Intellectual Property Organization (WIPO) | – | International search |
| EP0142337A1 | Cites | European Patent Office (EPO) | Y | Search report |
| GB2099007A | Cites | United Kingdom | XD | Search report |
4 priority claims, no other members on record
Priority claims4
| Document | Office | Kind | Date |
|---|---|---|---|
| 3814208 | Germany | A | |
| 3814208 | Germany | – | |
| DE19883814208 | – | – | – |
| 3814208 | – | – | – |
8 legal events, as the office reported them to INPADOC
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| Event | Code | |
|---|---|---|
| Application withdrawn (corrected)WithdrawnR18W | R18W | |
| Application withdrawnWithdrawn18W | 18W | |
| Designated contracting statesAK | AK | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: THE APPLICATION HAS BEEN WITHDRAWNSTAA | STAA | |
| Search report despatchedORIGINAL CODE: 0009013PUAL | PUAL | |
| Request for examination filed17P | 17P | |
| Designated contracting statesAK | AK | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI |
Numbers
- Publication
- 0341205
- Publication, DOCDB
- 0341205
- Publication, EPODOC
- EP0341205
- Application
- 89810306
- Application, DOCDB
- 89810306
- Application, EPODOC
- EP19890810306
Titles6
- German
- Farbstoffauffänger.
- English
- A dye scavenger.
- French
- Un produit captant les colorants.
- German
- Farbstoffauffänger
- English
- A dye scavenger
- French
- Un produit captant les colorants
Classification
- CPC, 6
- D06P5/08
- C11D3/0021
- C11D3/3703
- D06P1/5242
- D06P1/5278
- D06P1/5285
- IPC, 5
- D06L1 12
- C11D3 00
- C11D3 37
- D06P1 52
- D06P5 08
Designated states9
- Contracting states, 9
- Belgium
- Switzerland
- Germany
- Spain
- France
- United Kingdom
- Italy
- Liechtenstein
- Netherlands (Kingdom of the)