EP4143378A1 - Verfahren zum nachführen der färbung von fasern, garnen, geweben und kleidungsstücken - Google Patents
Verfahren zum nachführen der färbung von fasern, garnen, geweben und kleidungsstückenInfo
- Publication number
- EP4143378A1 EP4143378A1 EP20735032.3A EP20735032A EP4143378A1 EP 4143378 A1 EP4143378 A1 EP 4143378A1 EP 20735032 A EP20735032 A EP 20735032A EP 4143378 A1 EP4143378 A1 EP 4143378A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pigment
- tracking
- dyeing method
- fibre
- treated
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 79
- 238000004043 dyeing Methods 0.000 title claims abstract description 73
- 239000004744 fabric Substances 0.000 title description 18
- 239000000049 pigment Substances 0.000 claims abstract description 100
- 239000000835 fiber Substances 0.000 claims abstract description 53
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 31
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000011159 matrix material Substances 0.000 claims abstract description 17
- 230000008859 change Effects 0.000 claims abstract description 16
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- 239000012766 organic filler Substances 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims abstract description 6
- 238000011049 filling Methods 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 239000000975 dye Substances 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 239000007850 fluorescent dye Substances 0.000 claims description 6
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical class [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 5
- 239000008213 purified water Substances 0.000 claims description 4
- 229910000166 zirconium phosphate Inorganic materials 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 150000001412 amines Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- PMPJQLCPEQFEJW-HPKCLRQXSA-L disodium;2-[(e)-2-[4-[4-[(e)-2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC=C1\C=C\C1=CC=C(C=2C=CC(\C=C\C=3C(=CC=CC=3)S([O-])(=O)=O)=CC=2)C=C1 PMPJQLCPEQFEJW-HPKCLRQXSA-L 0.000 claims description 3
- 230000003287 optical effect Effects 0.000 claims description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims description 2
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 claims description 2
- 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 claims description 2
- 239000000980 acid dye Substances 0.000 claims description 2
- 239000000987 azo dye Substances 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 230000004044 response Effects 0.000 abstract description 5
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- 102000004169 proteins and genes Human genes 0.000 description 6
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- 238000011282 treatment Methods 0.000 description 6
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- -1 siloxanes Chemical class 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 238000012512 characterization method Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 229910001701 hydrotalcite Inorganic materials 0.000 description 3
- 229960001545 hydrotalcite Drugs 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000003550 marker Substances 0.000 description 3
- 239000001117 sulphuric acid Substances 0.000 description 3
- 235000011149 sulphuric acid Nutrition 0.000 description 3
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 2
- 239000005695 Ammonium acetate Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- RJZNFXWQRHAVBP-UHFFFAOYSA-I aluminum;magnesium;pentahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Al+3] RJZNFXWQRHAVBP-UHFFFAOYSA-I 0.000 description 2
- 235000019257 ammonium acetate Nutrition 0.000 description 2
- 229940043376 ammonium acetate Drugs 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 239000007767 bonding agent Substances 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
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- 150000003335 secondary amines Chemical class 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 210000000085 cashmere Anatomy 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
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- 238000013461 design Methods 0.000 description 1
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- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
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- 230000007613 environmental effect Effects 0.000 description 1
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- 238000009776 industrial production Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
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- 230000001404 mediated effect Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000002103 nanocoating Substances 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
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Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5264—Macromolecular compounds obtained otherwise than by reactions involving only unsaturated carbon-to-carbon bonds
- D06P1/5292—Macromolecular compounds obtained otherwise than by reactions involving only unsaturated carbon-to-carbon bonds containing Si-atoms
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/004—Dyeing with phototropic dyes; Obtaining camouflage effects
Definitions
- This invention relates to a tracking and imperceptible dyeing method for fibres, yarns, fabrics and garments.
- the invention relates to a cold dyeing method characterised by temperatures of below 70 °C with an overall treatment time of less than two hours and which does not use strong mineral acids.
- This method uses as trackers multi- responsive hybrid pigments, subsequently referred to as ‘smart pigments', and uses organo-functionalised siloxanes previously hydrolysed as binding agents for dyeing said fibres, yarns, fabrics and garments, with the aim of producing textile products with special characteristics of traceability and imperceptibility.
- the reactivity is guaranteed by a rapid diffusion of the acid substances, with a low molecular weight, towards the carboxylic groups of the fibre which are protonated in this way.
- a high level of protonation characterised by the presence of functional groups such as COOH, and taking advantage of the amphoteric nature of the protein fibres, several reactive points are obtained, characterised by the formation of NH3 + type groups.
- This cationic form interacts with the ionic dye (X-), dissolved in the aqueous bath, thus forming an anionic complex with strong electrostatic interaction between the protein-based fibre and the colour.
- the times and temperatures of the various dyeing baths vary according to the type of dye chosen.
- the legal infringement is not only related to the quality and safety of counterfeit products, but also to the circumvention of entire production systems and supply chains, where the companies that are legally designated to produce yarns, fabrics, garments and clothing accessories are suffering a substantial reduction in sales due to the introduction of counterfeit products into their distribution channels. Some of these counterfeit products have high quality standards.
- the competition between two production systems, one legal and one illegal, which operate in parallel and in a synchronized way to produce objects of the same quality and design, pushes legal companies to adopt sophisticated security systems and tracing elements.
- These safety systems must be such as to guarantee and certify the originality of the products and to be able to trace the textile elements and/or components at each production stage.
- the state of the art highlights systems for marking and tracing yarns, for example with fluorescent, phosphorescent or photochromic compounds, or labels fitted with electronic chips.
- the reactions to bind the marker are complex, or the preparation of the system containing the marker is not simple.
- the preparation of the system containing the marker is not simple.
- the prior art methods for tracking fabrics are mostly represented by labels to be applied to the garments before they are sold in order to certify the originality of the finished product to the final consumer.
- the technical problem raised and resolved by the invention is that of providing a method for marking and tracking textile yarns which allows the above-mentioned drawbacks of the prior art to be overcome.
- the aim of the invention is to provide an innovative tracking dyeing method, consisting of an imperceptible tracking yarn made of natural coloured and/or raw fibre, dyed with a smart pigment.
- This pigment is a 2D nano-structuring pigment, capable of piezochromic, piezo-photochromic and optionally fluorescent activity.
- the possible fluorescent activity of the pigment can be advantageously detected when the textile product is subjected to UV radiation at any stage of production, distribution and sales.
- the application of the tracking dyeing method according to the invention avoids the counterfeiting of the textile product, as the tracking element, that is, the textile fibre marked with the smart pigment, has particular properties upstream and downstream of the dyeing treatment which can only be traced by the owner of the technology.
- the response of the smart 2D nano-structuring pigment, when fluorescent is very similar to other systems with fluorescent activity already available on the market, it differs in that it can be multi-responsive, that is, it can also present piezochromic and photochromic activity and have a higher light fastness than current fluorescent-based security systems.
- the dyeing method according to the invention which uses the above mentioned pigment type, makes it possible to obtain a nano-coating or surface coating of pigment on the fibre in a single step and under bland conditions (below 60 °C), through the formation of a covalent bond between the fibre and the pigment, regardless of the type of fibre or textile clothing product.
- This makes it advantageously possible to transfer the starter characteristics of the pigment, such as the fluorescence, to the natural fibre, making the pigment imperceptible when fixed to the textile structure and therefore not easy to detect and counterfeit.
- the result of the dyeing method according to the invention is a clothing textile product preferably fluorescent with high fastness to light, photo-oxidative degradation, washing and all subsequent processes to which the fabric is subjected, such as overdyeing and bleaching.
- Textile products dyed with the dyeing method according to the invention are advantageously used as tracers to uniquely mark or identify fibres and/or yarns and/or fabrics and/or garments, also hereinafter meaning textile clothing accessories and to make a marked textile clothing accessory imperceptible to the naked eye, but visible when subjected to pressure and/or when irradiated under UV light and characterised by high light fastness.
- the textile products marked at the various processing stages by the method according to the invention are compatible with any subsequent processing of the textile process.
- the fabrics obtained with the method according to the invention not only attest to the originality of the product but are also able to trace the fabric itself, which is advantageous, for example, for Huawei fashion houses which commission the production lines of certain garments.
- the tracking dyeing method according to the invention uses a smart piezochromic pigment which preferably also has a photochromic and fluorescent activity and which, when fixed to a textile product, transfers these activities to the textile substrate providing a traceable textile product.
- the method of dyeing the textile product according to the invention advantageously allows the substrate to be dyed in such a way as to fix the pigment without producing a significant change of colour in the starter product, but making it optically active under UV radiation.
- the smart pigment applied to the textile substrate is such that it remains imperceptible to mere observation and thus maintains the original colour, quality and coat of the substrate even after the finishing treatments usually carried out on the textile products into which the treated textile substrate has been woven, including dyeing or over-dyeing operations.
- the dyeing method according to the invention is able to increase the compatibility between the textile product and the smart pigment, as it allows the formation of a thermally stable covalent bond between the fabric and the smart pigment.
- the fibre, yarn, fabric and/or garment obtained with this dyeing method are in fact covalently bound to the marker, that is, to the pigment, show piezochromic activity and, preferably, are also optically active under UV radiation.
- the fibre, yarn, fabric, treated and/or marked garment is uniquely identified as genuine, that is, by simple observation under conventional UV sources if the pigment is fluorescent.
- the method according to the invention is advantageously applicable to all categories of protein fibres and does not use aggressive substances such as strong mineral acids.
- the method according to the invention produces a fabric with excellent properties from the point of view of guaranteeing security and authenticity, thanks to the unique characteristics of the smart pigment.
- the multi-responsive, and in particular fluorescent, response of the smart pigment is, in fact, a guarantee of the originality of the textile products as well as the originality of the tracking system used.
- the dyeing method according to the invention also makes it possible to preserve the noble characteristics of the natural fibres, such as softness and brilliance, as the dyeing operations are carried out at temperatures not exceeding 60 °C and in less than 2 hours.
- the temperature ramp is fast and fully compatible with the normal operations of adding the yarn to be treated, dispersing the pigment or dye and adding the siloxane bonding agent, all in a time not exceeding 15 - 25 mins.
- Figure 11 which shows a diagram of the method according to the invention wherein a wool yarn is used and a siloxane bonding agent Flydrosyl 2926 of between 5 and 10% by weight with respect to the weight of the fibre and a smart pigment of between 0.25 and 2% by weight with respect to the weight of the fibre
- the maximum dyeing temperature applied in the method according to the invention represents the minimum temperature used in the traditional methods shown in Figures 1 , 2, and 3.
- a further advantage of the dyeing method according to the invention is that it does not discriminate the type of pigment, so the same procedure can be applied for the smart pigments based on lamellar solids type LDH and Zr phosphates.
- this invention provides an imperceptible yarn, obtained with a multi-responsive pigment, covalently bound to the yarn or textile product by a bland dyeing method and in a single industrial production step, with UV activity and high light fastness.
- Figure 1 shows a known dyeing process of wool in a strongly acidic bath
- Figure 2 shows a known dyeing process of wool in a weakly acidic bath
- Figure 3 shows a known dyeing process of wool in a neutral bath
- Figure 4 shows a yarn of treated (a) and untreated (b) wool according to example 1 , subjected to UV radiation;
- Figure 5 shows a yarn of treated (a) and untreated (b) wool according to example 1 , seen with the naked eye;
- Figure 6 shows a white treated (a) and untreated (b) yarn according to example 1 , subjected to UV radiation;
- Figure 7 shows the image obtained under the scanning electron microscope (SEM) of the white treated (a) and untreated (b) yarn of Figure 6;
- Figure 8 shows a graph obtained with EDX (Energy Dispersive X- ray Analysis) for the white treated (a) and untreated (b) yarn of Figure 6;
- Figure 9 shows a yarn of treated (a) and untreated (b) wool according to example 2, seen with the naked eye;
- Figure 10 shows a white treated (a) and untreated (b) yarn according to example 2, subjected to UV radiation.
- FIG 11 shows a schematic view of an application example of the tracking dyeing process according to the invention.
- A immersion of the wool yarn in purified water and addition of the siloxane agent;
- B addition of the smart pigment.
- a tracking dyeing method for the colouring or dyeing of a natural fibre to be marked or identified comprising the steps of: a) preparing a natural fibre in a dye tank; b) adding a siloxane agent in said tank; subsequently c) dispersing a liquid colouring solution comprising a pigment in said tank; d) heating the dye tank comprising the natural fibre, the siloxane agent and the colouring solution at a temperature comprised between 50 °C and 70 °C, preferably at 60 °C; e) keeping the temperature constant for a time comprised between 1 and 3 hours; wherein the pigment is a piezochromic pigment, comprising:
- the pigment has a first configuration, at a first pressure value P1 , wherein the inorganic matrix lamellae are spaced apart and at least one organic filling layer is positioned between two of the lamellae, and a second configuration, at a second pressure value P2, the value of the second pressure P2 being higher than the value of the first pressure P1 , wherein the above-mentioned inorganic matrix lamellae are close together allowing a molecular aggregation of said organic filler.
- the molecular aggregation generates a change in pigment coloration such that, in a configuration of use of the pigment applied to the support surface, when compression is applied to a portion of the treated support surface, the pigment changes from the first to the second configuration, resulting in a change in coloration of the portion of the treated surface that has been subjected to compression with respect to the remaining treated surface not subjected to compression allowing a marking or identification of authenticity of the treated support surface.
- said molecular aggregation generates a change in pigment coloration so that, in a second configuration of use of the pigment once activated (piezochromic) and applied on the support surface, when UV irradiation is applied on a portion of the treated support surface, the pigment changes from a first coloration to a second coloration (photochromic), resulting in a change in colour and a fluorescent response of the portion of the treated surface which has undergone UV irradiation with respect to the remaining treated surface that has not undergone irradiation, allowing marking or identification of authenticity of the treated support surface.
- the above-mentioned pigments, or smart pigments consist of said organic filler comprising organic molecules, optionally fluorescent, intercalated and/or adsorbed in said inorganic matrix, or inorganic substrate, the latter consisting of a lamellar solid, preferably of the layered double hydroxide type - LDH.
- the pigments are characterised by a nano-structuring 2D structure, and can have multi- responsive activity, that is, piezochromic (colour change with pressure), piezophotochromic (colour change with pressure and further colour change after radiation with LED and/or UV light and/or solar radiation), and fluorescent.
- the tracking dyeing process comprises the immersion of the fibres, yarns, fabrics and/or garments previously wetted in a solution containing the organo-functionalised siloxane agent and, subsequently, the smart tracer pigment, preferably fluorescent, is added to the dyeing bath.
- the method according to the invention confers to the fabric the above-mentioned characteristics thanks to the mode and the stage of application of said siloxane agent, preferably made up of organo- functionalised siloxanes.
- the siloxane agent, or binder agent, based on previously hydrolysed organo-functionalized siloxanes is used to create a coating to the support, meaning yarn, fibre, fabric or garment, and then the smart pigment without organic coating is added. Therefore, the fibre is firstly made reactive with respect to the smart pigments thanks to the appropriate chemical modification, or functionalization of the support, with the organo-functionalised siloxane agent, inserted at an earlier stage with respect to the smart pigment.
- the application of the method according to the invention leads to the formation of covalent bonds between the inorganic matrix of the smart pigment and the functional groups of the fibre or natural textile substrate, such as primary and secondary amine, hydroxyl and carboxylic groups.
- the covalent bond is formed by the reaction between reactive organo-functional siloxane agents (adhesion promoters), the natural fibres, such as wool, silk, linen, cotton, hemp, cashmere and their mixtures and the pigments, in water and under mild thermal conditions.
- reactive organo-functional siloxane agents adheresion promoters
- the natural fibres such as wool, silk, linen, cotton, hemp, cashmere and their mixtures and the pigments
- the siloxane agent reactive in an aqueous medium, is in fact preferably activated at a temperature below 60 °C.
- the mild heat treatment promotes the formation of a rapid condensation reaction between the hydroxyl groups (-OH) of the inorganic matrix and the residual functional groups present in the natural fibres (hydroxyl, carboxyl and primary and secondary amines), mediated by the presence of the siloxane agent, which promotes the adhesion.
- the various organic functions (amine, epoxy, alkoxide) contained in the adhesion promoter additive are able to react in the medium, producing by-products such as diols and alcohols, and covalently bind the textile fibres with the pigments used.
- the dyed product thus obtained is highly resistant to further hydrolysis, bleaching and washing reactions.
- the textile product dyed by the method according to the invention is characterised by imperceptibility of the tracking element, that is, of the pigment.
- imperceptibility means, on a visual level, the fact of not being able to perceive a substantial difference in colour that may originate in the textile product to be tracked according to the presence, within it, of the treated textile substrates, that is, a difference DE not greater than 0.5 when calculated according to the criteria of ISO 105 Part J03 "Calculation of colour differences" on the basis of the CMC formula (2:1).
- the treated textile substrates that is, the tracker yarns
- the treated textile substrates are preferably used in a very dispersed manner within the warp or weft yarns making up the textile product to be tracked. More specifically, it is preferable to use a percentage of tracker yarn not exceeding 1%, distributed randomly within an article on the basis of technical calculations, which gives rise to a "warp note” and/or “weaving note” and/or “weave”.
- the liquid colouring solution can comprise a mixture of purified water and pigment wherein said pigment has a concentration by weight of between 0.85% and 5%.
- the liquid colouring solution can comprise a percentage by weight of pigment comprised between 0.1% and 5%, optionally 2%, with respect to the weight of the natural fibre.
- the siloxane agent is added in the tank in a percentage by weight of less than or equal to 20%, optionally comprised between 5% and 10%, with respect to the weight of the natural fibre.
- the tracking dyeing method according to the invention may further comprise a step for homogenising a dye bath comprising the fibre and the siloxane agent or may comprise a step for homogenising a dye bath comprising the fibre, the siloxane agent and the colouring solution. More specifically, the homogenising step is preferably carried out for a time comprised between 10 and 20 minutes.
- the natural fibre is placed in water and the ratio between the fibre and the water can be comprised between 1 mg/ml and 20 mg/ml.
- the pH is kept equal to the isoelectric point of the natural fibre. Even more preferably, the pH is kept in a range of values comprised between 4 and 7.
- the fibre can be in a configuration wound on a spool, or reel, or skein.
- the inorganic matrix of the piezochromic pigment may include components belonging to the hydrotalcites group. More specifically, components belonging to the hydrotalcites group are preferably layered double hydroxides (LDH), optionally MgAI and ZnAI, or lamellar solids such as zirconium phosphates, for example alpha zirconium phosphate type B or zirconium phosphate.
- LDH layered double hydroxides
- MgAI and ZnAI optionally MgAI and ZnAI
- lamellar solids such as zirconium phosphates, for example alpha zirconium phosphate type B or zirconium phosphate.
- the organic filling of the piezochromic pigment may include aggregation-induced emission compounds (AIEs), and/or water-soluble dyes, and/or optical brighteners, and/or fluorescent dyes, and/or azo dyes, and/or liquid crystals, and/or carboxylic acids, and/or anthroquinone dyes, and/or acid dyes.
- the fluorescent dyes preferably comprise Fluorescent Brightener, optionally Fluorescent Brightener 351 , or acid fluorescent dyes of group I.
- the siloxane agent can be selected among amine / epoxy / octyl / methoxy / ethoxy functionalised hydrolysed siloxane agents, optionally Dynasylan Hydrosil 1153, Dynasylan Hydrosil 2627, Dynasylan Hydrosil 2926, Dynasylan Hydrosil 2776, Dynasylan Hydrosil 2909.
- Example 1 Tracking dyeing method according to the invention for the application of a smart piezophotochromic pigment with fluorescent properties on wool yarns and characterisation of the yarn obtained.
- a spool of natural yarn such as wool, silk, cotton, linen and natural fibre blends was placed in the dyeing tank and distilled water was added at a ratio of 10/1 mg of fibre per ml of water.
- LDH_FB351 which has fluorescent piezophotochromic properties composed of an inorganic lamellar solid type component belonging to the family of layered double hydroxide (LDH) known as hydrotalcite, with the formula [M 2+ i-xM 3+ x(0H)2][An ]x/ n -zH20 (3:1 Mg/AI ratio, co-intercalated with counterion nitrate and/or water and/or carbonate molecules - MgAI-LDH CAS 148884-57-5) intercalated with the organic molecule belonging to the family of optical brighteners or fluorescent brighteners named Fluorescent Brightener 351 (CAS 54351 - 85-8) was dispersed in water (10 mg/ml), considering the pigment at 2% with respect to the fibre weight.
- LDH_FB351 which has fluorescent piezophotochromic properties composed of an inorganic lamellar solid type component belonging to the family of layered double hydroxide (LDH) known as hydrotalcite, with the
- a siloxane organic binder agent Dynasylan ® Hydrosil 2926 (Evonik) was added to the tank with the yarn (5 times the weight of the pigment), left in circulation for 10 mins and then the pigment dispersion was added.
- the mixture was heated at 60 °C for 2 hours, preferably 1 hour.
- the bath water was then removed from the skein/spool by discharging the dyeing water and the resulting yarn was rinsed two to three times.
- Table 1 shows the colorimetric characteristics of the pigment used.
- images of UV radiation ( Figure 6) and an SEM image ( Figure 7) are shown with an EDX graph ( Figure 8) on a white treated yarn and a white untreated yarn. More specifically, the white treated yarn appears more expanded to the naked eye, with the fibres further apart, whilst the white untreated yarn appears more compact to the naked eye, with the fibres closer together.
- the colour fastness to light, washing and over-dyeing on the treated wool yarn was verified, obtaining the fluorescent response degradation results shown below, visually evaluated in light boxes, based on the grayscale for degradation ISO 105 A02, using the light source of a Blacklight-Blue BLB-T8 fluorescent tube.
- the grayscale for degradation assigns values ranging from grade 5: no colour change to grade 1 : maximum colour change, also comprising intermediate grades. Test results
- Example 2 Method of tracking dyeing, according to the invention, natural yarns made of protein fibre - wool, with fluorescent piezochromic smart pigments named LDH_AIE, consisting of the organic molecule 4,4'- (1 ,2-Diphenylethene-1 ,2-diyi)dibenzoic acid (cas n° 1002339-79-8) co intercalated in a precursor hydrotalcite type Aluminium Magnesium Hydroxide Nitrate- LDH_N03 (cas 148884-57-5).
- LDH_AIE fluorescent piezochromic smart pigments
- LDH_AIE consisting of the organic molecule 4.4'-(1.2-Diphenylethene-1.2-diyl) dibenzoic acid co-intercalated in an inorganic component consisting of precursor hydrotalcite type Aluminium Magnesium Hydroxide Nitrate- LDH_N03 (CAS 148884-57-5) was dispersed in water (10 mg/ml), considering the pigment at 2% with respect to the fibre weight.
- Table 2 shows the colorimetric characteristics of the pigment used.
- Figures 9 and 10 show the treated and untreated wool yarn, respectively observed with the naked eye and under UV radiation.
- Example 3 Example of the tracking dyeing method according to the invention.
- the method for dyeing yarns by means of smart pigments according to the invention described below is a spool dyeing process compatible with an industrial process (Process A) and comprises the following steps: 1. Inserting the spool into the dyeing tank;
- Bath ratio 1 :17 (The bath ratio specifies how much water must be present depending on the weight of the yarn). More specifically, a range of between 1 :15 - 1 :17 indicates narrow baths, while a value of 1 :20 may indicate long baths);
- Example 4 Example of the tracking dyeing method according to the invention.
- the method for dyeing yarns by means of smart pigments according to the invention described below is a skein functionalisation and dyeing process compatible with an industrial process (Process B-1) and comprises the following steps: (a) placing the yarn in water (1-20 mg/ 1 ml);
- step (b) checking the pH of the water of step (a).
- the best conditions for dyeing are in the range of 4-12, preferably 4-7;
- c) preparing the dispersion of the smart pigment in water (1-20 mg/ml), with a percentage of smart pigment in the range of 0.1-5% according to the fibre weight;
- d) adding a siloxane agent to the water obtained in step (b) with a siloxane/fibre ratio by weight in the range of 1/4 to 1/10 (that is, between 0.1 and 0.25);
- step (e) adding the dispersion of smart pigment in water obtained in step (c) to the water with the yarn and siloxane obtained in step (d);
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ITPG20120006A1 (it) * | 2012-02-15 | 2013-08-16 | Ferrini S R L | Metodo per tinteggiare fibre tessili naturali e relative sostanze |
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