EP1171663A1

EP1171663A1 - Treatment agents for textiles, method of producing same and their use

Info

Publication number: EP1171663A1
Application number: EP00910847A
Authority: EP
Inventors: Helmut-Martin Meier; Ferdinand Kümmeler; Detlev Kierspe; Peter Selinger; Jacob-Cornelis Dijks; Winfried Guth
Original assignee: Bayer AG
Current assignee: Bayer AG
Priority date: 1999-03-29
Filing date: 2000-03-16
Publication date: 2002-01-16
Also published as: US6528576B1; TR200102760T2; CA2365686A1; JP2002541339A; WO2000058547A1; AU3290200A

Abstract

The invention relates to treatment agents for textiles which contain bisulfite-blocked polyisocyanate prepolymers and special softening formulations. The treatment agents can be applied to textile materials by means of all known finishing methods, notably by exhaustion. The finished textile materials are characterized by their very good hydrophily, soft handle and excellent anti-electrostatic properties.

Description

Textile treatment agents. Process for their preparation and their use

The invention relates to textile treatment agents containing bisulfite-blocked polyisocyanate

Contain prepolymers and special plasticizer formulations, a process for the preparation of these textile treatment agents and their use.

The modification of the handle of textile materials is of great importance. The shrink-free finish to prevent shrinking, shrinking and shrinking of textile goods under the influence of moisture is an important part of the textile finishing. DE-PS 24 14 470 describes, for example, the finishing of textile materials with bisulfite-blocked polyisocyanate prepolymers. These bisulfite-blocked polyisocyanate prepolymers are prepared by reacting polyisocyanates with polyhydroxy compounds and then blocking the isocyanate end groups with bisulfite. Since the bisulfite-blocked polyisocyanate prepolymers are self-crosslinking compounds, no catalysts need to be added in the finishing step. However, it is disadvantageous that the bisulfite-blocked polyisocyanate prepolymers are not the same in all known textile finishing processes

Success can be used.

From US-A-3,898,197 and GB-A-1,062,564 bisulfite-blocked polyisocyanate prepolymers are known, which can be used to modify keratin fibers.

However, the freedom from pumping that can be achieved by finishing with the bisulfite-blocked polyisocyanate prepolymers and influencing the grip of the textile materials generally lead to a significantly reduced softness of the finished materials. For this reason, plasticizers are usually added to the equipment to compensate for this disadvantage. An overview of the various known types of plasticizers and their properties are contained in the publication by P. Hardt, Melliand Textilberichte 9/1990, p. 699.

From JP 09195167 A2, in particular, cationic plasticizer compositions with polyhydric alcohols are known. DE-OS 19 629 666 also describes the use of alkyl polyglycosides for the hydrophilic adjustment of polypropylene and polyester fibers. DE-OS 31 38 181 describes plasticizer mixtures which contain fatty acid amides.

The use of these substances in the finish leads to a very soft one

Handle of textile materials. However, all known plasticizers have the common disadvantage that they usually contain a long hydrophobic residue. This hydrophobic residue in turn means that the treated textiles absorb water poorly. This hydrophobicity is particularly disturbing for towels, bathrobes and terry towels.

The object of the present invention was therefore to provide a self-crosslinking textile treatment agent which at the same time gives the textile material good hydrophilicity, a good soft feel and a high surface smoothness. In addition, the textile treatment agent should be able to be used as widely as possible in all known textile finishing processes and, in particular, should have such a liquor stability that it can be applied to textiles by means of nozzle dyeing apparatus.

The invention relates to textile treatment agents which are characterized in that they contain two components K1 and K2 in a weight ratio of (0.1-5): 1, where

Kl represents a mixture that (A) 0-30% by weight of polyalcohols which can be obtained by reacting formaldehyde with ketones which carry at least 4 replaceable hydrogens adjacent to the carbonyl group in the presence of alkaline catalysts,

(B) 0-30% by weight of polyalcohols which have at least two OH groups and do not fall under the definition of A),

(C) 0.1-10 wt .-% adducts of C ₁₂ -C ₂ fatty acids or C ₈ -C ₁₈ fatty alcohols or -C ₂ -C36 alkyl or Di ^ C ^ -C _ß g ^ alkylamines or C9-C ₂ 4-alkyl phenols with 2- 100 mol ethylene oxide, and

(D) 70-99.9% by weight of an aqueous plasticizer formulation, the 10-90% by weight of plasticizer compounds, based on the aqueous plasticizer formulation,

contains, where (A) + (B) is> 0.1% by weight, based on the sum of the individual components (A) to (D),

and component K2 is a polyisocyanate prepolymer, the isocyanate groups of which are in bisulfite-blocked form.

The polyalcohols (A) of component Kl can be obtained by reacting formaldehyde with ketones which carry at least 4 replaceable hydrogen atoms adjacent to the carbonyl group, the reaction being carried out in the presence of alkaline catalysts.

The ketones preferably have the general formula (1)

in which

R and R 'independently of one another represent straight-chain or branched C ₁ -C 2 ₄ alkyl, C ₁ -C ₂₄ alkenyl, phenyl or naphthyl

or both R and R 'together can also form an alkylene - (- CH ₂ -) - _p with p = 2-6, it being possible for one or two CH ₂ groups to be replaced by a hetero atom, preferably oxygen,

m 0 or 1 and

n is 0, 1, 2, 3 or 4.

R and R 'are preferably independently of one another -CH3, -C ₂ H ₅ , -C3H7, -i-C3H ₇ , -C4H9, -CH = C (CH ₃ ) ₂ or together form an alkylene radical

-CH: with p = 2 or 3.

The straight-chain or branched C _j -C ₂₄ alkyl or -CC ₂₄ alkenyl groups of the radicals R and R 'are optionally substituted by OH, COOH or SO3H. The phenyl or naphthyl radical can also be substituted by OH, COOH or SO3H.

Preferred radicals R and R 'are those of the formulas -CH ₂ -COOH and -CH ₂ -C (CH ₃ ) ₂ (OH).

Alicyclic ketones such as cyclopentanone and cyclohexanone have proven particularly useful; aliphatic ketones such as acetone, methyl ethyl ketone, methyl propyl ketone, methyl isopropyl ketone, methyl butyl ketone, methyl isobutyl ketone, methyl sec-butyl ketone, mesityl oxide, diacetone alcohol, levulinic acid, diethyl ketone, diacetyl, acetyl acetone, acetyl ketone or methylbenzene are particularly suitable. Formaldehyde can be used in the form of paraformaldehyde, trioxymethylene or a formaldehyde polymer that releases formaldehyde under the reaction conditions.

Polyalcohols (A) according to formulas 2 (1) to 2 (8) which can be obtained via the above-mentioned reaction are particularly preferred in component C1.

Suitable alkaline catalysts are e.g. Oxides or hydroxides of alkali or

Alkaline earth metals. Alkaline earth metal hydroxides, in particular calcium hydroxide, are preferably used. The preparation of the polyalcohols (A) is generally described in US Pat. No. 2,462,031, to which express reference is hereby made.

The polyalcohols (B) of component Kl have at least two OH groups and do not fall under the definition of the polyalcohols (A).

Suitable polyalcohols (B) are e.g. Pentaerythritol, neopentyl glycol, ethylene glycol, diethylene glycol, triethylene glycol, trimethylolpropane, glycerol, polyglycerol, dipentaerythritol, diglycerol, glucose and carbohydrates with more than 2 OH groups.

The ethylene oxide adducts (C) of component Kl are adducts of C1 ₂ -C ₂₂ fatty acids or Cg-Cig fatty alcohols or C ^^ g-alkyl- or di- (C ₁₂ -C36) alkylamines or C ₉ -C24 alkylphenols with 2-100 mol ethylene oxide (see, for example, Tensid-Taschenbuch by W. Stache, 2nd edition, 1981, pp. 617-662).

Particularly preferred ethylene oxide adducts (C) are e.g. Adducts of stearyl alcohol with 19, 56 or 95 mol ethylene oxide, from oleyl alcohol with 19, 56 or 95 mol ethylene oxide, from stearic acid with 6.5, 8.5 or 10 mol ethylene oxide, from oleic acid with 6.5, 8.5 or 10 mol ethylene oxide, or adducts from tallow fatty amine with 2, 4.5, 10, 22 or 25 moles of ethylene oxide.

The components contained in the aqueous plasticizer formulation (D) are described in detail, for example, in DE-OS 31 38 181, to which reference is hereby expressly made. These are, for example, aqueous mixtures containing Ml

50-80% by weight of component (I), which are acylated alkanolamines which can be obtained by reacting saturated or unsaturated C ₂ -C _{2 2} -carboxylic acids with alkanolamines which have 1 or 2 nitrogen atoms, 1 - 3 OH groups and 2 - 6 carbon atoms contain, in a molar ratio

(1-3): 1, 10 - 30% by weight of component (II), which is water-soluble, quaternary ammonium salts of the general formula (3)

is what

R ^{1 is} a C ₄ -C ₂ 5 -alkyl or alkenyl radical which is interrupted by an amide and / or ester group,

R ^{2 is} a radical with the meaning of R ¹ or a C ₁ -C ₄ alkyl radical,

R ³ and R ⁴ independently of one another are a C _j -C ₄ alkyl radical, a hydroxyethyl, a hydroxypropyl or a benzyl radical and

X ^{t_ is} a t-fold negatively charged anion, where t is 1, 2 or 3,

2 - 20 wt .-% of component (III), which are fatty acid esters from saturated or unsaturated Ci ₂ -C22 fatty acids or saturated or unsaturated C ^ -C _j o-dicarboxylic acids and mono- to tetravalent C3-C _2Q -Alcohols,

2 - 20 wt .-% of component (IV), which are ethylene oxide adducts of Ci ₂ "C ₂₂ fatty acids or Cg-C _j g fatty alcohols or C ^ -C g alkyl or Di ^ C ^^^ - alkylamines or C ₉ -C ₂₄ - alkylphenols with 2-100 mol ethylene oxide, and 0 - 25% by weight of component (V), which are diorganopolysiloxanes with a viscosity of 1,000 to 100,000 mm ² / s,

where all of the above weight percentages are based on the entire mixture Ml and the sum of components (I) to (V) in the mixture Ml 10-

90 wt .-% results.

The acylated alkanolamines (I), which are described, for example, by K. Lindner, "Tenside-Textilhilfsmittel-Waschrohstoffe", 2nd edition, volume 1, pages 904 and 993, and by Schwartz-Perry "Surface Active Agents" 1949, vol. 1, p. 173, contain amide and / or ester groups, depending on the alkanolamines used.

Carboxylic acids of natural or synthetic origin are used in their production, e.g. Lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid or their mixtures, as described e.g. made from coconut oil, palm kernel oil or tallow, or branched chain acids from oxosynthesis, e.g. Isostearic acid, or the acid chlorides of these carboxylic acids. Technical quality stearic acid and behenic acid are preferably used.

Suitable alkanolamines containing 1-3 OH groups and having 2-6 C atoms include monoethanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, N- (2-aminoethyl) ethanolamine, 1-aminopropanol and bis- (2-hydroxy- propyl) - amine. N- (2-Aminoethyl) ethanolamine, monoethanolamine and diethanolamine are preferably used.

The water-soluble quaternary ammonium salts (II) contain as hydrophobic residue at least one C _j4 -C ₂₅ alkyl or alkenyl chain which is interrupted by an amide and / or ester group. For their preparation, mono-, according to known methods, which are described for example in Schwartz-Perry "Surface Active Agents", 1949, Vol. 1, p. 118 and in E. Jungermann "Cationic Surfactants" 1970, p. 29.

Di- or triamines, which have a tertiary amino group and one or two primary ones Contain amino groups and / or one or two OH groups, acylated with the acids mentioned under I) and then suitably quaternized.

In formula (3), R ¹ preferably represents the radical R ⁵ -CO-YR ⁶ -, where R ^{5 is} an alkyl or alkenyl radical having 12 to 22 carbon atoms, R ^{6 is} an ethylene or propylene radical and Y is NH or O. .

In formula (3) the anion X ^{t_ is} preferably chloride, bromide, sulfate, phosphate, methosulfate or dimethyl phosphite.

Suitable amines for the preparation of (II) are e.g. 3-amino-1-dimethylamino-propane, 3-amino-1-diethylamino-propane, methyl-bis- (3-amino-propyl) -amine, bis- (2-methylamino-ethyl) -methylamine, 2-dimethylamino- ethanol, methyl bis (2-hydroxyethyl) amine or 3-dimethylamino-l-propanol.

Preferred compounds (II) are reaction products of technical stearic acid or behenic acid with 3-amino-1-dimethylamino-propane or 3-amino-1-diethylamino-propane, which are quaternized with dimethyl sulfate or dimethyl phosphite.

The quaternization is carried out by customary methods without a solvent or in a solvent, and in addition to water or ethanol, the acylated alkanolamines (I) can also serve as solvents in molten form, provided that they do not contain a tertiary nitrogen atom.

Suitable quaternizing agents are, for example, methyl chloride, dimethyl sulfate, dimethyl phosphite or ethylene oxide, the reaction in the latter case being carried out in sulfuric acid or phosphoric acid solution.

The substances of the two substance groups (I) and (II) can also be combined in one

Prepare one-pot process by mixing mixtures for both groups the amines mentioned are reacted with fatty acids and the proportion of tertiary amino groups is then quaternized accordingly.

Mono- to tetravalent C3-C20 alcohols are used to prepare the carboxylic acid esters (III). The alkyl chain of these alcohols can also be interrupted by oxygen.

Examples of the carboxylic acid esters (III) are butyl stearate, 2-ethylhexyl stearate, octa-decyl stearate, isotridecyl stearate, 2-ethylhexyl oleate, di-2-ethylhexyl sebacate, pentaethylene glycol dilaurate, trimethylolpropane trilaurate and pentaerythritol tetrapelargonate.

Components (I), (II) and (III) are plasticizer compounds.

To improve the solubility of the mixtures of softener compounds are used as component (IV) ethylene oxide adducts of _Cj2-C22 fatty acids, Cg-Cjg- fatty alcohols, C ^ -C g _ß-alkyl- or di- _(C1 -C36) -alkylamines or C9-C ₂₄ - used alkylphenols. These components (IV) also have plasticizer properties due to the long alkyl residues. The optimal degree of alkoxylation differs from case to case and can be from 2-100 mol ethylene oxide per mol starting substance.

If required, diorganopolysiloxanes (V) with viscosities of 1000 to 100,000 ramVs can be added to the mixtures of the plasticizer compounds by emulsion polymerization. These diorganopolysiloxanes are usually used as aqueous emulsions and also have plasticizer properties. Polydimethylsiloxanes are preferred.

In a further embodiment, the aqueous mixture also contains Ml 1-30% by weight of a component (VI), which is an oxidized polyethylene wax emulsion,

this weight percent of component (VI) also being based on the total mixture Ml and the sum of components (I) to (VI) in the mixture Ml

Is 10-90% by weight.

These oxidized polyethylene wax emulsions (VI) usually have an acid number of 10 to 60 mg KOH / g and are described, for example, in DE-OS 30 03 851 and DE-OS 28 30 173, to which reference is hereby expressly made.

A mixture M2 can also be used as the aqueous plasticizer formulation (D)

2-20% by weight of component (IV) already defined for the mixture Ml,

0 - 25% by weight of the component (V) and

1 - 30% by weight of component (VI) already defined for the mixture Ml

contains, wherein all of the above-mentioned% by weight data are based in each case on the entire mixture M2 and the sum of components (IV), (V) and (VI) in the mixture M2 is 10-90% by weight.

As an aqueous plasticizer formulation (D), a mixture M3 for

Use that

50-80% by weight of component (I) already defined for the mixture Ml,

10-30% by weight of component (II) already defined for the mixture Ml, 2-20% by weight of component (III) already defined for the mixture Ml,

1-20% by weight of component (IV) already defined for the mixture Ml,

1-30% by weight of component (VI) and already defined for the mixture Ml

1-20% by weight of a component (VII), which is a cationic

Emulsifier acts by the addition of 2-20 mol

Ethylene oxide and / or propylene oxide is obtained on a C ₀ -C ₂ alkylamine in the presence of an organic or inorganic acid,

contains, with all the above wt .-% - each based on the entire mixture M3 and the sum of components (I), (II), (III), (IV), (VI) and (VII) in the mixture M3 gives 10-90% by weight.

The cationic emulsifier (VII) contained in the mixture M3 is obtained by adding 2-20 mol of ethylene oxide and / or propylene oxide to a C 1 -C ₂₂ -alkylamine in the presence of an organic or inorganic acid. For example, formic acid, acetic acid,

Phosphoric acid, phosphorous acid, hydrochloric acid, sulfuric acid or sulfurous acid can be used.

A mixture M4 can also be used as the aqueous plasticizer formulation (D)

1 - 20% by weight of component (IV) already defined for the mixture Ml,

1 - 30% by weight of component (VI) and already defined for the mixture Ml

1 - 20% by weight of component (VII) already defined for the mixture M3 contains, with all of the above wt .-% - each based on the entire mixture M4 and the sum of components (IV), (VI) and (VII) results in 10 - 90 wt .-%.

A mixture M5 can also be used as the aqueous plasticizer formulation (D)

0.1-5% by weight of component (IV) already defined for the mixture Ml,

60-90% by weight of component (VI) already defined for the mixture Ml,

1-10% by weight of a component (VIII), which is a branched polysiloxane / polyether copolymer,

0.5-5% by weight of a component (IX), which is an organic phosphoric acid salt, and

0-1% by weight of fragrances (X)

contains, with all of the above-mentioned% by weight data being based in each case on the entire mixture M5 and the sum of components (IV), (VI) and (VIII) in the mixture M5 being 10-90% by weight.

Component (VIII) is a branched polysiloxane / polyether copolymer. For example, a branched polysiloxane / polyether copolymer is suitable, which is obtainable by reacting octamethyltetrasiloxane, methyltrichlorosilane and polyglycols started from ethylene oxide and / or propylene oxide with a hydroxyl number of 20-40 mg KOH / g on alkanols, preferably butanol . Component (IX) is, for example, organic phosphoric acid salts from mono- or di- (C] -C ₁₈ -alkyl) phosphates and hydroxy- (C ₁ - C ₄ ) -alkylamines. Alkali or alkaline earth phosphates can also be used.

A mixture M6 can also be used as the aqueous plasticizer formulation (D)

50-80% by weight of component (I) already defined for the mixture Ml,

10 - 30% by weight of component (II) already defined for the mixture Ml,

2 - 20% by weight of component (III) already defined for the mixture Ml,

1 - 20% by weight of the component (IV) and component already defined for the mixture Ml

1-80% by weight of a component (XI), which is polydimethylsiloxane with a viscosity of less than 40 mPas at 23 ° C,

contains, with all of the above wt .-% given to the entire

Mix M6 are related and the sum of components (I), (II), (III), (IV) and (XI) in the mixture M6 is 10 - 90 wt .-%.

A mixture M7 can also be used as the aqueous plasticizer formulation (D)

1 - 80% by weight of the component (XI) already defined for the mixture M5 contains, with all of the above-mentioned percentages by weight being based in each case on the entire mixture M7 and the sum of components (IV) and (XI) in the mixture M7 being 10-90% by weight.

A mixture M8 for. Can also be used as the aqueous plasticizer formulation (D)

Use that

0.1-20% by weight of component (IV) already defined for the mixture Ml

0 - 25% by weight of the component (V) and

5-40% by weight of a component (XII) which is an amino silicone,

contains, with all of the above wt .-% given to the entire

Mix M8 are related, as well as

1-40% by weight based on component (XII), an amphoteric surfactant (XIII) and 0-50% by weight based on component (XII), a straight-chain or branched monohydric C 1 -C ₈ alcohol (XIV)

the sum of the wt .-% of components (IV), (V) and (XII) in the mixture M8 gives 10-90 wt .-%.

All usual and commercially available aminosilicones which are liquid at room temperature can be used as aminosilicones (XII), preference being given to N-modified, particularly preferably N-acylated and in particular N-formylated aminosilicones. N-acylation means the introduction of the radical -COR or -CONHR (R = H or Ci-Cig-alkyl). Such aminosilicones are described in detail, for example, in EP-A-0 417 559. All known and commercially available surfactants can be used as amphoteric surfactants (XIV). Those from the class of the C ₈ -C ₄ alkylamine oxides are preferably used.

The straight-chain or branched monohydric C 1 -C ₁₈ alcohols (XIV) can be, for example, aliphatic, cycloaliphatic, araliphatic alcohols or ether alcohols. For example, ethanol, propanol, butanol, isobutanol, cyclohexanol, butyl diglycol or benzyl alcohol are suitable.

A mixture M9 can also be used in the aqueous plasticizer formulation (D)

0 - 80% by weight, preferably 50-80% by weight, of component (I) already defined for the mixture Ml,

0-30% by weight, preferably 10-30% by weight, of component (II) already defined for the mixture Ml,

0-20% by weight, preferably 2-20% by weight, of those already defined for the mixture M1

Component (III),

0-20% by weight of component (IV) already defined for the mixture Ml,

0 - 50% by weight of component (VI) already defined for the mixture Ml,

0 - 80 wt .-% of a component (XV), which is the reaction product of a saturated or unsaturated C ₈ -C ₂₂ carboxylic acid with amines selected from the group consisting of diethylenetriamine, triethylenetetramine and dimethylamino-propylamine, 0 - 50 wt .-% of a component (XVI), which is a paraffin with a melting point of 50-120 ° C,

0 - 50% by weight of a component (XVII), which is a vegetable oil, preferably refined rapeseed oil,

0 - 30% by weight stearoyl sarcoside (XVIII),

0 - 80% by weight of a component (XIX) which is sulfonated beef tallow,

0 - 50% by weight of a component (XX) which is paraffin sulfonic acid or its alkali metal or alkaline earth metal salts,

contains, with all of the above wt .-% given to the entire

Mixture M9 and the sum of components (I), (II), (III), (IV), (VI), (XV), (XVI), (XVII), (XVIII), (XIX) and ( XX) results in the mixture M9 10 - 90 wt .-%.

In the mixture M9, the acylated alkanolamines (I), can, as already described, by reaction of saturated or unsaturated C ₁₂ -C 2 ₂ -carboxylic acids with alkanolamines containing 1 or 2 nitrogen atoms, 1 - 3 OH groups and 2 - Contain 6 carbon atoms, are available in a molar ratio (1-3): 1, also be quaternized or protonated. Suitable quaternizing agents are, for example, methyl chloride, dimethyl sulfate, dimethyl phosphite or ethylene oxide, in the latter

If the reaction is carried out in sulfuric or phosphoric acid solution.

In the mixture M9, component (XV) can also be quaternized, protonated or with C -C ₈ -diisocyanates, preferably hexamethylene diisocyanate (HDI), 4-methyl-m- phenylene diisocyanate (TDI) or 4,4'-methylene bis (phenyl isocyanate) (MDI).

Component (XVII) is a vegetable oil; refined rapeseed oil, which consists essentially of emcasic acid, is preferably used as

Triglyceride with oleic, linoleic and linolenic acid.

Component (XVIII) is the reaction product of stearic acid chloride and sarcosine, optionally also in the form of an alkali metal, in particular sodium, salt.

The component (XIX) is based on beef tallow as animal fat, which contains various proportions of myristic acid, palmitic acid, stearic acid, oleic acid and linoleic acid in the form of the respective triglycerides. This beef tallow is e.g. sulfonated using oleum and neutralized with alkali.

Component (XX) is a paraffin sulfonic acid or its salts. Suitable paraffin sulfonic acids or salts include straight-chain, branched, saturated or unsaturated hydrocarbons with 12-20 C atoms which have sulfonic acid groups and / or sulfonate groups. Component (XX) has a surface-active effect.

The above-described aqueous mixtures M1 to M9 are prepared by heating the respective components of these mixtures above the melting point, if necessary, and with stirring after adding a corresponding one

Amount of preferably warm water stirred homogeneously. After cooling to room temperature, aqueous plasticizer formulations (D) are obtained in the form of stable liquid solutions or emulsions which contain 10-90% by weight, preferably 10-80% by weight, of plasticizer compounds, based on the aqueous plasticizer formulation. The aqueous mixtures Ml to M9 obtained in this way become component K1 of the textile treatment agent according to the invention added. Component K1 of the textile treatment agents according to the invention is produced by mixing the respective components (A) - (D) in any order.

Preferred components are those which contain 0-20% by weight of polyalcohols (A),

0-20% by weight of polyalcohols (B), 0.1-8% by weight of ethylene oxide adducts (C) and 80-95% by weight of the plasticizer formulation (D), the sum of (A) and (B) is> 0.1% by weight, based on the sum of the individual components (A) to (D).

Also preferred are components K1

(A) 0.1-30% by weight of the compound of the formula 2 (5),

but do not contain component (B).

Also particularly preferred are components K1

(A) 0.1-30% by weight of the compound of the formula 2 (5),

no component (B), (C) 0.1-10% by weight adducts of C ₁₂ -C ₂₂ fatty acids or Cg-C _j g fatty alcohols or Ci ₂ -C3g alkyl or di- (C _j2 -C ₃ 6) - alkylamines or C9-C2 ₄ alkyl phenols with 2-100 mol ethylene oxide, and

(D) 70-99.9% by weight of an aqueous plasticizer formulation containing 10-

90% by weight of plasticizer compounds, based on the aqueous plasticizer formulation,

contain, with all of the above wt .-% - each based on the component Kl and used as the aqueous plasticizer formulation (D) one or more of the mixtures Ml to M9 described above.

Also preferred are components K1

(B) 0.1-30% by weight of a polyalcohol which has more than two OH groups and does not fall under the definition of (A),

but do not contain component (A).

Here, as component (B) in particular trimethylolpropane, pentaerythritol,

Glucose or mixtures of these compounds are used.

Also particularly preferred are components K1

no component (A), (C) 0.1-10 wt .-% adducts of C ₁₂ -C ₂ 2-fatty acids or Cg-C ₁₈ - fatty alcohols or alkylamines C ₁₂ "36" alkyl or di (C ₁₂ -C 3 ₆₎ or C9-C ₂₄ alkyl phenols containing from 2-100 moles of ethylene oxide, and

(D) 70-99.9% by weight of an aqueous plasticizer formulation containing 10-

contain, with all of the above-mentioned% by weight in each case based on the components K1 and one or more of the mixtures Ml to M9 described above being used as the aqueous plasticizer formulation (D).

The polyisocyanate prepolymers used as component K2, the isocyanate groups of which are in a form blocked with bisulfite, are known in principle. Their manufacture is described, for example, in US-A-3,898,197, GB-A-1,062,564 and DE-PS-

24 14 470, to which express reference is hereby made. The polyisocyanate prepolymers have an average of at least two isocyanate groups blocked with bisulfite and have no free isocyanate groups. The bisulfite-blocked polyisocyanate prepolymers preferably have a functionality of 2-4.

The bisulfite-blocked polyisocyanate prepolymers are usually prepared by first reacting excess amounts of polyisocyanates with polyhydroxy compounds. The use of the excess polyisocyanate ensures that all the hydroxy groups react and the reaction product, the so-called polyisocyanate prepolymer, contains free isocyanate groups. These free isocyanate groups are then blocked with bisulfite, especially sodium or potassium bisulfite.

The polyhydroxy compounds to be used to prepare the polyisocyanate prepolymers have at least two hydroxyl groups. It is preferred di- or trifunctional polyhydroxy polyethers in the molecular weight range 500-10000, in particular 1000-5000, which are obtained by alkoxylation of di- or trifunctional starter molecules, such as water, ethylene glycol, 1,2-propanediol, 1,3-propanediol, triethanolamine , 1,2,6-hexanetriol, trimethylolpropane or glycerol are accessible in a known manner. Amines such as primary or secondary alkyl and aryl amines, diamines or polyamines are also suitable as starter molecules for the polyhydroxy polyethers. Ethylene diamine, propylene diamine or hexamethylene diamine is preferably used as the starter. Preference is given to those polyethers in the production of which either exclusively propylene oxide or else propylene oxide together with up to 50 mol% of ethylene oxide, based on the total amount

Ethylene oxide and propylene oxide have been used. The latter "mixed" polyethers can be both those which have the propylene oxide and ethylene oxide units in a random distribution and the known block polyethers which have polypropylene oxide and polyethylene oxide blocks. A block copolymer with 55% propylene oxide and 45% ethylene oxide units started on ethylenediamine, which naturally has a functionality of approximately 4, has proven particularly useful.

The polyisocyanates to be used for the production of the polyisocyanate prepolymers are preferably aliphatic, cycloaliphatic or aromatic polyisocyanates. Diisocyanates of the formula OCN- (CH ₂ ) _n -NCO, in which n is an integer from 2-16, in particular 4-6, have proven suitable as aliphatic polyisocyanates. For example, hexamethylene diisocyanate and tetramethylene diisocyanate are preferred. Suitable cycloaliphatic polyisocyanates are, for example, the diisocyanates l-isocyanato-3,3,5-trimethyl-5-isocyanato-methylcyclohexane, 4,4'-

Diisocyanatodicyclohexylmethane, 1,4-diisocyanatocyclohexane and 2,4-diisocyanatohexahydrotoluene. Such aliphatic and cycloaliphatic polyisocyanates can be used either individually or in a mixture. As aromatic polyisocyanates e.g. 2,4-toluenediisocyanate, 2,6-toluenediisocyanate, commercially available mixtures of 2,4-toluenediisocyanate and 2,6-toluenediisocyanate,

4,4'-diphenylmethane diisocyanate or the isomeric xylene, benzene or naphthalene diisocyanates, preferably p-xylylene diisocyanate. These aromatic polyisocyanates can also be used individually or in a mixture, mixtures of aliphatic, cycloaliphatic and / or aromatic polyisocyanates also being usable.

The polyisocyanate prepolymers are prepared by reacting an excess of the polyisocyanate (e.g. a 2-10 times molar excess) with the polyhydroxy polyether. If necessary, unreacted amounts of the polyisocyanate are subsequently removed.

The blocking of the polyisocyanate prepolymer obtained with the sodium or potassium bisulfite can be carried out in such a way that the prepolymer is dissolved in an organic water-compatible solvent and an aqueous solution of the bisulfite is then added to this solution. However, it is also possible to work without an organic solvent. It is also possible to work with the addition of organic or inorganic acids. If an organic solvent is used, this can, if desired, be removed by distillation from the aqueous solution obtained after the blocking reaction. Even when using hydrophobic polyethers, which mainly contain polypropylene oxide units, the hydrophilic bisulfite-blocked isocyanate groups generally ensure sufficient solubility of the product in water. If necessary, however, complete removal of the organic solvent is dispensed with or additional organic solvent is added to the system. In general, the proportions of bisulfite-blocked polyisocyanate prepolymer and organic solvent are such that 20-80% by weight of prepolymer and 80-20% by weight of solvent are present in the aqueous solution, which is either pure water or a mixture from water with up to 80 vol.% of organic solvent. Particularly suitable water-compatible solvents are those which have a boiling point below 150 ° C. Ethyl acetate, acetone, ethanol or isopropanol are preferably used. Components K1 and K2 are present in the textile treatment agents according to the invention in a weight ratio of (0.1-5): 1 and preferably of (0.4-2.5): 1.

Apart from the above-mentioned components K1 and K2, the textile treatment agent according to the invention can also contain other constituents which are customary for textile auxiliaries. These include protective colloids, perfumes, fungicides or bactericides, foam suppressants and UN protective agents.

For easier handling, it has proven useful to prepare aqueous preparations from the textile treatment agents according to the invention. These aqueous preparations contain 10-90% by weight, preferably 30-70% by weight, of the textile treatment agents according to the invention.

The invention further relates to a process for finishing natural and synthetic textile materials, in which these textile materials are treated with the text treatment agents according to the invention or their aqueous preparations.

In particular, this process is carried out by treating the textile materials with the textile treatment agents or their aqueous preparations in the exhaust process (reel runners, nozzle-dyeing unit) or in the dipping, spraying or padding process. For these methods of applying the textile treatment agents according to the invention to the textiles, US Pat. No. 3,898,197,

GB-A-1,062,564 and DE-PS-24 14 470.

The textile treatment agents according to the invention are preferably used in an amount of 0.5-5% by weight, preferably 1-4% by weight in the exhaust process or with 5-50 g / 1 liquor, preferably 10-40 g / 1 liquor in the padding process, based on a 100% fleet intake. The liquor ratios can vary between 1: 1 and 1: 30 depending on the type of application.

It has proven to be particularly advantageous to apply the textile treatment agents according to the invention in the exhaust process from a short liquor with nozzle dyeing systems

To apply textiles.

The invention further relates to natural and / or synthetic textile materials which have been finished with the textile treatment agents according to the invention or their aqueous preparations.

The textile materials that can be used can be natural and / or synthetic

Fiber materials exist. Suitable natural fiber materials are, for example, cellulose fibers such as cotton, viscose or rayon wool, as well as wool or silk. As synthetic fibers e.g. Polyamide, polyester or polyacrylonitrile can be used.

The textile treatment agents according to the invention considerably improve the hydrophilicity of the treated textile materials, while maintaining the soft feel and the high surface smoothness.

Another advantage of the textile treatment agents according to the invention is their excellent absorption behavior. While the component K2 (bisulfite-blocked polyisocyanate prepolymer) known in principle is very difficult to apply to textiles alone in the exhaust process, the combination of components K1 and K2 in the textile treatment agent according to the invention enables the exhaust process to be carried out while maintaining a permanently finished, hydrophilic textile material. This result is unexpected, since a combination of component K2 with a plasticizer of the prior art (for example that described in DE-OS-31 38 181), like component K2 alone, leads only to an insufficient liquor extraction when used in the exhaust process . An additional advantage of the textile treatment agents according to the invention is that textile materials which have been equipped with these textile treatment agents have a considerably reduced surface resistance and thus anti-electrostatic properties. What is particularly surprising here is the permanence of these anti-electrostatic properties: the reduced surface resistance is still present even after several washes of the textile material.

The textile treatment agents according to the invention also have advantageous behavior when stored at low temperatures. In the case of textile treatment agents which contain customary plasticizer compositions of the prior art with, for example, paraffins and waxes, the active substances precipitate out in solid form under the influence of low temperatures and cannot be emulsified even by heating. In the case of the textile treatment agents according to the invention, on the other hand, it is possible at any time without any problems to obtain reusable emulsions.

Examples 1-18:

Polyester Helanca Interlock is used as the textile substrate.

The application of the inventive and the comparative textile treatment agents described below is carried out by the exhaust process. The tests are carried out on an AHIB A device with a liquor ratio of 1:20. The inventive and comparative textile treatment agents are used in an amount of 5-50 g / l of liquor.

The handle and hydrophilicity of the treated materials are assessed and the transparency of the liquor is assessed. If the fleet is clear, this means that the textile treatment agent is extracted. If, on the other hand, the fleet appears cloudy, the textile treatment agent has not been completely removed.

Hydrophilicity: the water drop test is used to check the time within which a water drop is absorbed by the substrate.

Handle assessment: carried out on terry goods by 6 people each by awarding a ranking, the mean value of which is given. A grip of 3 is still acceptable.

Component Kl:

The following aqueous mixture Ml is first prepared for component K1:

The following plasticizer formulations 1-8 are produced as component D for component Kl:

Component K2:

To produce component K2, 1.55 mol of polyether P1 are reacted with 4.65 mol of hexamethylene diisocyanate at 80-85 ° C. After reaching a viscosity of 3500-4000 mPas, the reaction product obtained is added to 3.88 mol NaHSO ₃ (used as a 40% aqueous solution) and 0.62 mol acetic acid is added. The solids content of the solution is adjusted to 30% by adding water.

The polyether P1 is produced by reacting 1 mol of ethylenediamine with 13 mol of propylene oxide and 14 mol of ethylene oxide at 130-140 ° C.

The following textile treatment agents are used:

Textile treatment agent V 1: (comparison 1)

Textile treatment agent 1: (according to the invention)

Textile treatment agent 2: (according to the invention)

Textile treatment agent V 2: (comparison 2)

Textile treatment agent V 3: (comparison 3)

Textile treatment agent V 4: (comparison 4)

Textile treatment agent V5: (comparison 5)

Textile treatment agent 3: (according to the invention)

Textile treatment agent 4: (according to the invention)

Textile treatment agent 5: (according to the invention)

Textile treatment agent 6: (according to the invention)

Textile treatment agent 7: (according to the invention)

Textile treatment agent 8: (according to the invention)

Textile treatment agent 9: (according to the invention)

Table 1 below shows the properties of the polyester samples treated in each case.

Examples 12 and 13: (antistatic finish)

The material used is 100% polyester fine satin and equipped with textile treatment agents 1 and V3 as described above. The amount of textile treatment agent used is 40 g / 1 liquor.

The finished material is washed 5 x 25 minutes at 40 ° C in a roller bath, then dried for 10 minutes at 40 ° C and kept in a dry climate for 48 hours.

Before and after the washing described above, the surface resistance of the finished textile material is measured with a ring electrode according to the DIN 54345 method. The results are summarized in Table 2 below and are compared with the corresponding surface resistances which are measured on the unfinished polyester fine satin.

Claims

claims

1. Textile treatment agent, characterized in that it contains two components Kl and K2 in a weight ratio of (0.1-5): 1, Kl being a mixture which

(A) 0-30% by weight of polyalcohols which can be obtained by reacting formaldehyde with ketones which carry at least 4 replaceable hydrogens adjacent to the carbonyl group in the presence of alkaline catalysts,

(B) 0-30% by weight of polyalcohols which have at least two OH groups and do not fall under the definition of (A),

(C) 0.1-10% by weight adducts of C ₁₂ -C ₂₂ fatty acids or C ₈ -C ₁₈ fatty alcohols or C ₁ 2-C ₃₆ alkyl or di (C ₁₂ -C 36) - alkylamines or C ₉ -C ₂₄ alkylphenols with 2-100 mol ethylene oxide, and

(D) 70-99.9% by weight of an aqueous plasticizer formulation, the 10-90% by weight of plasticizer compounds, based on the aqueous

Plasticizer formulation,

contains, where (A) + (B)> 0.1 wt .-%, based on the sum of the individual components (A) to (D), and component K2 is a polyisocyanate prepolymer whose isocyanate Groups are present in a form blocked with bisulfite.

2. Textile treatment composition according to claim 1, characterized in that the polyisocyanate prepolymer in the form of an aqueous preparation with a content of 10-70% by weight, preferably 20-50% by weight, of the polyisocyanate

Prepolymers is used. Textile treatment agent according to Claim 1 or 2, characterized in that the polyalcohols (A) in component Kl are compounds of the formulas 2 (1) to 2 (8).

Textile treatment agent according to one or more of claims 1-3, characterized in that the polyalcohols (B) of component Kl are pentaerythritol, neopentylglycol, ethylene glycol, ethylene glycol, triethylene glycol, trimethylolpropane, glycerol, polyglycerol, dipentaerythritol, diglycerol, glucose or carbohydrates with more than 2 OH groups.

Textile treatment agent according to one or more of claims 1-4, characterized in that in the case of ethylene oxide adducts (C) the components nente Kl adducts of stearyl alcohol with 19, 56 or 95 mol ethylene oxide, from oleyl alcohol with 19, 56 or 95 mol ethylene oxide, from stearic acid with 6.5, 8.5 and 10 mol ethylene oxide, from oleic acid with 6.5, 8.5 or 10 mol ethylene oxide, or from Tallow fatty amine with 2, 4.5, 10, 22 or 25 moles of ethylene oxide.

6. Textile treatment composition according to one or more of claims 1-5, characterized in that it is an aqueous solution of a mixture Ml in the aqueous plasticizer formulation (D) of component Kl

(I) 50-80 wt .-% acylated alkanolamines of saturated or unsaturated C _j2 -C2 _2-carboxylic acids and alkanolamines containing 1 or 2 nitrogen atoms, 1 - 3 OH Gmppen and 2 - 6 C-atoms, in a molar ratio ( 1-3): 1,

(II) 10-30% by weight of water-soluble, quaternary ammonium salts of the general formula (3)

wonn

R ^{1 is} a C ^ -C ^ alkyl or alkenyl radical which is interrupted by an amide and / or ester group,

R ^{2 is} a radical with the meaning of R ¹ or a C _j -C ^ alkyl radical, R ³ and R ⁴ independently of one another are a C _j -C ₄ alkyl radical, a hydroxyethyl, a hydroxypropyl or a benzyl radical and

X ^{t_ is} a t-negatively charged anion, where t is 1,

Is 2 or 3.

(III) 2 - 20 wt .-% fatty acid ester of saturated or unsaturated C ₂ -C 22 fatty acids or saturated or unsaturated C ₄ -C 1 ₀ - dicarboxylic acid and monohydric to tetrahydric _{_C3-2} 0- alcohols,

(IV) 2-20% by weight of ethylene oxide adducts of C ₁₂ -C ₂ fatty acids or C ₈ -C ₁₈ fatty alcohols or C ₁₂ -C ₃₆ alkyl or di (C ₁₂ -C ₃₆ ) - alkyl amines or C9-C2 ₄ alkylphenols with 2-100 mol ethylene oxide and

(V) 0 to 25% by weight of diorganopolysiloxanes with a viscosity of 1,000 to 100,000 mm ² / s,

is.

Textile treatment agent according to Anspmch 6, characterized in that the aqueous mixture Ml additionally

1-30% by weight of a component (VI), which is an oxidized polyethylene wax emulsion,

contains, whereby this weight% indication of component (VI) is based on the entire mixture Ml and the sum of components (I) to (VI) in the mixture Ml is 10-90% by weight.

8. Textile treatment agent according to one or more of claims 1-5, characterized in that it is an aqueous solution of a mixture M2 containing in the aqueous plasticizer formulation (D) of component Kl

2-20% by weight of component (IV) already defined for the mixture Ml,

0 - 25% by weight of the component (V) and

1 - 30% by weight of component (VI) already defined for the mixture Ml

acts, with all of the above-mentioned% by weight data being based in each case on the entire mixture M2 and the sum of components (IV), (V) and (VI) in the mixture M2 being 10 to 90% by weight.

9. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formulation (D) of component Kl containing an aqueous solution of a mixture M3

50-80% by weight of component (I) already defined for the mixture Ml,

10-30% by weight of component (II) already defined for the mixture Ml,

2-20% by weight of component (III) already defined for the mixture Ml,

1-20% by weight of component (IV) already defined for the mixture Ml,

1-30% by weight of component (VI) and already defined for the mixture Ml 1-20 wt .-% of a component (VII), which is a cationic

Emulsifier acts by the addition of 2-20 mol

Ethylene oxide and / or propylene oxide is obtained over a C ₁ oC ₂₂ alkylamine in the presence of an organic or inorganic acid,

acts, with all the above wt .-% - each based on the entire mixture M3 and the sum of components (I), (II), (III), (IV), (VI) and (VII) in the mixture M3 yields 10 - 90% by weight.

10. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formulation (D) of component Kl containing an aqueous solution of a mixture M4

1 - 20% by weight of component (IV) already defined for the mixture Ml,

1 - 30% by weight of component (VI) and already defined for the mixture Ml

1 - 20% by weight of the component (NU) already defined for the mixture M3

acts, with all of the above wt .-% given to the entire

Mixture M4 are related and the sum of components (IN), (VI) and (VII) results in 10 - 90 wt.%.

11. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formu- lation (D) of component Kl containing an aqueous solution of a mixture M5

0.1-5% by weight of component (IV) already defined for the mixture Ml,

60-90% by weight of component (VI) already defined for the mixture Ml,

0-1% by weight of fragrances (X)

acts, with all the above-mentioned% by weight data being based in each case on the entire mixture M5 and the sum of components (IV), (VI) and (VIII) in the mixture M5 being 10-90% by weight.

12. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formulation (D) of component Kl containing an aqueous solution of a mixture M6

50-80% by weight of component (I) already defined for the mixture Ml,

10-30% by weight of component (II) already defined for the mixture Ml,

2 - 20% by weight of component (III) already defined for the mixture Ml, 1 - 20% by weight of the component (IV) and component already defined for the mixture Ml

1-80% by weight of a component (XI), which is polydimethylsiloxane with a viscosity of less than 40 mPas at 23 ° C

, with all of the above-mentioned percentages by weight being based in each case on the entire mixture M6 and the sum of components (I), (II), (III), (IV) and (XI) in the mixture M6 10-90 % By weight results.

13. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formulation (D) of component Kl containing an aqueous solution of a mixture M7

1 - 80% by weight of the component (XI) already defined for the mixture M5

acts, with all of the above weight percentages being based in each case on the entire mixture M7 and the sum of components (IV) and (XI) in the mixture M7 being 10-90% by weight.

14. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formulation (D) of component Kl containing an aqueous solution of a mixture M8

0.1-20% by weight of component (IV) already defined for the mixture Ml 0 - 25% by weight of the component (V) and

5-40% by weight of a component (XII) which is an amino silicone,

acts, with all the above wt .-% - each based on the entire mixture M8, and further

1-40 wt .-% based on component (XII), an amphoteric surfactant

(XIII) and 0-50% by weight, based on component (XII), of a straight-chain or branched monohydric cis alcohol (XIV)

the sum of the% by weight of components (IV), (V) and (XII) in the mixture M8 gives 10-90% by weight.

15. Textile treatment agent according to one or more of claims 1-5, characterized in that it is in the aqueous plasticizer formulation (D) of component Kl containing an aqueous solution of a mixture M9

0-20% by weight, preferably 2-20% by weight, of component (III) already defined for the mixture Ml, 0-20% by weight of component (IV) already defined for the mixture Ml,

0 - 50% by weight of component (VI) already defined for the mixture Ml,

0 - 80 wt .-% of a component (XV), which is the

Reaction product from a saturated or unsaturated C ₁₈ -

C ₂ carboxylic acid with amines selected from the group

Diethylenetriamine, triethylenetetramine and dimethylaminopropylamine,

0 - 50 wt .-% of a component (XVI), which is a paraffin with a melting point of 50-120 ° C,

0 - 50 wt .-% of a component (XVII), which is a vegetable

Oil, preferably refined rapeseed oil,

0 - 30% by weight stearoyl sarcoside (XVIII),

0 - 80 wt .-% of a component (XIX), which are sulfonated

Beef tallow

acts, with all the above wt .-% - each based on the entire mixture M9 and the sum of components (I), (II), (III), (IV), (VI), (XV), (XVI ), (XVII), (XVIII), (XIX) and (XX) in the mixture M9 gives 10-90% by weight.

16. Textile treatment agent according to Anspmch 1, characterized in that the component Kl

(A) 0.1-30% by weight of a compound of the formula 2 (5),

but does not contain component (B).

17. Textile treatment agent according to Anspmch 1, characterized in that component K 1

but does not contain component (A).

18. Textile treatment agent according to Anspmch 8, characterized in that trimethylolpropane, pentaerythritol, glucose or mixtures thereof is used as component (B).

19. Aqueous preparations, characterized in that they contain 10-90% by weight, preferably 30-70% by weight, of the textile treatment agent according to one or more of claims 1-18.

20. A method for finishing natural and synthetic textile materials, characterized in that they are treated with the textile treatment agent according to one or more of claims 1-18 or the aqueous preparations according to Anspmch 19.

21. The method according to Anspmch 11, characterized in that the equipment takes place in the exhaust, immersion, spray or foulard process.

22. The method according to Anspmch 11, characterized in that the equipment takes place in the exhaust process from a short liquor with nozzle dyeing systems.

23. Natural or synthetic textile materials, characterized in that they have been equipped with the textile treatment agent according to one or more of claims 1 to 18 or the aqueous preparations according to Anspmch 19.