CN107938326A - The preparation method of binary compound coated fabric - Google Patents

The preparation method of binary compound coated fabric Download PDF

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Publication number
CN107938326A
CN107938326A CN201711227681.5A CN201711227681A CN107938326A CN 107938326 A CN107938326 A CN 107938326A CN 201711227681 A CN201711227681 A CN 201711227681A CN 107938326 A CN107938326 A CN 107938326A
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China
Prior art keywords
fabric
preparation
binary compound
compound coated
coated fabric
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Application number
CN201711227681.5A
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Chinese (zh)
Inventor
刘秋丽
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Shaanxi Gaohua Zhiben Chemical Technology Co Ltd
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Shaanxi Gaohua Zhiben Chemical Technology Co Ltd
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Priority to CN201711227681.5A priority Critical patent/CN107938326A/en
Publication of CN107938326A publication Critical patent/CN107938326A/en
Withdrawn legal-status Critical Current

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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/77Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
    • D06M11/79Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M10/00Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
    • D06M10/02Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements ultrasonic or sonic; Corona discharge
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/46Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/30Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/32Polyesters
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/01Stain or soil resistance
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/25Resistance to light or sun, i.e. protection of the textile itself as well as UV shielding materials or treatment compositions therefor; Anti-yellowing treatments

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

A kind of preparation method of binary compound coated fabric, belongs to field of material preparation, it is characterised in that:Deionized water and absolute ethyl alcohol are mixed, are uniformly mixed under magnetic stirring apparatus;Polyester-cotton fabric after processing is cut, is put into above-mentioned solution, continues ultrasound;At room temperature, butyl titanate is at the uniform velocity instilled in the above-mentioned solution containing fabric, keeps heating up under ultrasonic state;Fabric drying is taken out, obtains the fabric after titanium dioxide arranges;Silicon dioxide gel is added in above-mentioned solution with uniform speed slow, it is lower to continue to be ultrasonically treated, obtain the fabric after titania/silica arranges.Titania/silica binary compound coated fabric is prepared with ultrasonic in situ, significantly improves collection and anchoring capability of the fabric loose structure to disperse particles, the function persistence and washing fastness for making fabric are significantly improved.Meanwhile assign medical function and the persistence such as antibacterial fabric, automatically cleaning, uvioresistant.

Description

The preparation method of binary compound coated fabric
Technical field
The invention belongs to field of material preparation, more particularly to a kind of preparation method of binary compound coated fabric.
Background technology
It is more next with the continuous improvement of living standards of the people, requirement of the people to medical textile with the development of science and technology It is higher, to environmentally friendly and functional requirement also pay attention to day by day.In order to cater to the change of the market demand, medical textile has been assigned New intension, the science and technology in medical textile field are developed rapidly.Develop Durable antibacterial, self-cleaning function it is medical Textile, undoubtedly will create huge social and economic benefit for textile industry.Medical textile is after use inevitably Attachment dirt, the textile including medical sheet, operation dress, medical drapes etc., mainly using cotton and polyester fiber as raw material, Easily polluted by oily dirt, and textile fabric genus polyporus material, mushroom is easily adsorbed, the sweat of human body discharge, come off Sebum etc. all provide abundant nutrition for mushroom breeding.The growth of bacterium easily causes cross-infection and spreads the disease, and produces Peculiar smell, damages fiber, so developing has the function of that automatically cleaning, Durable antibacterial become very necessary requirement.
World's medical textile is continued to increase with annual 5% speed, and at home hospital with every 3 years of cloth with about 10 myriametres Speed increase.Medical textile inevitably adheres to dirt after use, and particularly medical sheet is mainly with cotton and terylene Fiber is raw material, is easily polluted by oily dirt, and textile fabric genus polyporus material, easily adsorbs mushroom, human body discharge Sweat, exuviae fat etc. all provide abundant nutrition for mushroom breeding.The growth of bacterium easily causes cross-infection and passes Disease is broadcast, produces peculiar smell, damages fiber.
The content of the invention
A kind of the present invention is intended to provide preparation method of binary compound coated fabric.
The preparation method of binary compound coated fabric of the present invention, includes the following steps:
(1)45ml deionized waters and 55ml absolute ethyl alcohols are mixed, it is 2.5 to add 0.5mLHCl and adjust pH value, magnetic stirring apparatus It is lower to be uniformly mixed;(2)Polyester-cotton fabric after processing is cut, is put into above-mentioned solution, continues ultrasound 5min;(3)At room temperature, 5mL butyl titanates are at the uniform velocity instilled in the above-mentioned solution containing fabric, keep being warming up to 65 DEG C under ultrasonic state, ultrasonic time 2h;(4)Fabric is taken out, 5min is dried at 80 DEG C, cures 3min at 120 DEG C, obtains the fabric after titanium dioxide arranges;(5) Silicon dioxide gel is added in above-mentioned solution with uniform speed slow, continues to be ultrasonically treated at 65 DEG C, obtains titanium dioxide/titanium dioxide Fabric after silicon arrangement.
The preparation method of binary compound coated fabric of the present invention, step(1)The mass fraction of the HCl is 36%.
The preparation method of binary compound coated fabric of the present invention, step(1)The rotating speed of the magnetic stirring apparatus is 250rpm;Mixing time is 5min.
The preparation method of binary compound coated fabric of the present invention, step(2)Ruler after the polyester-cotton fabric cutting Very little is 10 × 10cm.
The preparation method of binary compound coated fabric of the present invention, step(3)The instillation speed of the butyl titanate Spend for 50 μ L/s.
The preparation method of binary compound coated fabric of the present invention, step(5)The speed of the silicon dioxide gel For 100 μ L/s.
The preparation method of binary compound coated fabric of the present invention, step(5)The sonication treatment time is 2h.
The preparation method of binary compound coated fabric of the present invention, titanium dioxide/dioxy is prepared with ultrasonic in situ SiClx binary compound coated fabric, while solving nano-particle dispersion problem, significantly improves fabric loose structure to dividing The collection and anchoring capability, the function persistence and washing fastness for making fabric for dissipating particulate are significantly improved.Meanwhile assign fabric The medical functions such as antibacterial, automatically cleaning, uvioresistant and persistence.
Embodiment
The preparation method of binary compound coated fabric of the present invention, includes the following steps:(1)By 45ml deionized waters and 55ml absolute ethyl alcohols mix, and it is 2.5 to add 0.5mL and adjust pH value, is uniformly mixed under magnetic stirring apparatus;(2)By washing after processing Cotton fabric is cut, and is put into above-mentioned solution, continues ultrasound 5min;(3)At room temperature, 5mL butyl titanates are at the uniform velocity instilled State in the solution containing fabric, keep being warming up to 65 DEG C under ultrasonic state, ultrasonic time 2h;(4)Fabric is taken out, is dried at 80 DEG C 5min is done, cures 3min at 120 DEG C, obtains the fabric after titanium dioxide arranges;(5)Silicon dioxide gel is added with uniform speed slow Enter in above-mentioned solution, continue to be ultrasonically treated at 65 DEG C, obtain the fabric after titania/silica arranges.
The preparation method of binary compound coated fabric of the present invention, step(1)The mass fraction of the HCl is 36%. Step(1)The rotating speed of the magnetic stirring apparatus is 250rpm;Mixing time is 5min.Step(2)After the polyester-cotton fabric is cut Size be 10 × 10cm.Step(3)The instillation speed of the butyl titanate is 50 μ L/s.Step(5)The silica The speed of colloidal sol is 100 μ L/s.Step(5)The sonication treatment time is 2h.The particle diameter of TiO 2 particles is smaller, unit matter The population of amount is more, and specific surface area is bigger, is more carried out on the surface beneficial to light-catalyzed reaction, light-catalyzed reaction speed and effect Rate is also higher.When the size of particle is in 1~10nm, quantum effect just occurs, becomes quantization particle, cause significantly to prohibit Band broadens, so that hole-electronics is to will be with dimensional quantum degree with stronger oxidation-reduction ability, catalytic activity Raising and increase.The quantization of size also makes semiconductor obtain the charge migration speed of bigger, hole and compound several of electronics Rate greatly reduces, and is conducive to improve the speed of light-catalyzed reaction.Titanium dioxide can only be absorbed and be less than due to the limitation of energy gap The ultraviolet light of 387nm, in visible light part almost without absorption, this greatly reduces its utilization rate to sunlight.And multiple After closing graphene oxide, the absorption in visible region is remarkably reinforced.Moreover, the characteristic absorption for comparing titanium dioxide have it is bright Aobvious red shift, can significantly improve utilization rate of the titanium dioxide to sunlight, so as to improve it after illustrating combined oxidation graphene Photocatalytic activity.After this result can be attributed to combined oxidation graphene, the energy gap of titanium dioxide narrows, that is, The formation of Ti-O-C keys, causes it to absorb the sunlight of more low energy.
In addition, after composite silicon dioxide, Titanium dioxide absorption solar energy slightly strengthens, but changes no composite graphite Alkene is obvious.Analysis reason is probably silica as insulator, to a certain extent titanium dioxide energy gap can be made to broaden, but Si4+Ion enters titanium dioxide lattice, and part substitutes Ti4+Position, so as to form Ti-O-Si network structures, and network knot The formation of structure has the separation beneficial to semiconductor photoproduction electron-hole pair and the raising of quantum efficiency, improves light to a certain extent Catalytic activity.Since absorbance curve of the low concentration aqueous solution of methylene blue in ultraviolet-visible light area is relatively simple, especially can , only there is an absorption maximum in Jian Guang areas at 665nm, and the maximum excitation wavelength of anatase crystal is in 390nm or so, methylene blue Do not absorbed in this wave-length coverage, can to avoid the overlapping phenomenon of absworption peak, and methylene blue many material surfaces have compared with Good absorption property, anti-light degradation capability are stronger, it is easy to it is reacted and is detected, so molten using light degradation methylene blue Liquid evaluates titanium dioxide, the photocatalytic activity of polyester-cotton fabric after coating.Knitted with methylene blue solution percent of decolourization to assess polyester-cotton blend Thing automatically cleaning effect, specific method are:The methylene blue solution that 50mL concentration is 20mg/L is fitted into culture dish, respectively 4 Be put into a culture dish the polyester-cotton fabric, coating of titanium dioxide fabric, titania/silica coated fabric of the non-coatings of 1g with And titanium dioxide/graphene oxide coated fabric.Be placed on illumination under the fluorescent lamp of 20W, liquid level apart from light source center 25cm, Different time samples, and measures the absorbance change of methylene blue solution at wavelength 650nm with ultraviolet-visible spectrophotometer, Mapped with the relation of the variable quantity of methylene blue solution absorbance and light application time, and photocatalytic activity is represented with this.Do not having In the presence of having photochemical catalyst, methylene blue solution concentration under ultraviolet irradiation varies less;Titanium dioxide/oxidation The photocatalytic activity of graphene and titania/silica is strong compared with pure titinium dioxide, to Asia in the case of radiation of visible light 12h The degradation rate of methyl blue is respectively 40% and 31%.Being shown by granularmetric analysis, prepared photocatalytic particle reaches nanoscale, Nano particle diameter is minimum after wherein titanium dioxide/graphene oxide is compound, is 9.07nm.

Claims (7)

1. a kind of preparation method of binary compound coated fabric, it is characterised in that include the following steps:(1)By 45ml deionized waters Mixed with 55ml absolute ethyl alcohols, it is 2.5 to add 0.5mLHCl and adjust pH value, is uniformly mixed under magnetic stirring apparatus;(2)After handling Polyester-cotton fabric cut, be put into above-mentioned solution, continue ultrasound 5min;(3)At room temperature, 5mL butyl titanates are at the uniform velocity dripped Enter in the above-mentioned solution containing fabric, keep being warming up to 65 DEG C under ultrasonic state, ultrasonic time 2h;(4)Fabric is taken out, at 80 DEG C Lower drying 5min, cures 3min at 120 DEG C, obtains the fabric after titanium dioxide arranges;(5)By silicon dioxide gel with the uniform velocity slow Slowly add in above-mentioned solution, continue to be ultrasonically treated at 65 DEG C, obtain the fabric after titania/silica arranges.
2. the preparation method of binary compound coated fabric according to claim 1, it is characterised in that:Step(1)The HCl Mass fraction be 36%.
3. the preparation method of binary compound coated fabric according to claim 2, it is characterised in that:Step(1)The magnetic The rotating speed of power blender is 250rpm;Mixing time is 5min.
4. the preparation method of binary compound coated fabric according to claim 3, it is characterised in that:Step(2)It is described to wash Size after cotton fabric is cut is 10 × 10cm.
5. the preparation method of binary compound coated fabric according to claim 4, it is characterised in that:Step(3)The titanium The instillation speed of sour four butyl esters is 50 μ L/s.
6. the preparation method of binary compound coated fabric according to claim 5, it is characterised in that:Step(5)Described two The speed of silica sol is 100 μ L/s.
7. the preparation method of binary compound coated fabric according to claim 6, it is characterised in that:Step(5)It is described super The sonication time is 2h.
CN201711227681.5A 2017-11-29 2017-11-29 The preparation method of binary compound coated fabric Withdrawn CN107938326A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109537265A (en) * 2018-11-07 2019-03-29 温州格蕾斯服饰有限公司 A kind of antibacterial garment and its manufacture craft
CN109736075A (en) * 2018-12-28 2019-05-10 杭州蓝色倾情服饰有限公司 Uvioresistant fabrics and preparation method thereof
CN111567956A (en) * 2020-05-29 2020-08-25 邦威防护科技股份有限公司 Medical protective clothing
CN112878066A (en) * 2021-01-19 2021-06-01 绍兴佳卓新材料科技有限公司 Antibacterial corrosion-resistant anti-scaling food-grade nano composite coating and preparation method thereof
CN113174749A (en) * 2021-04-20 2021-07-27 红豆集团无锡红豆童装有限公司 Ultra-light organic cotton textile fabric and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109537265A (en) * 2018-11-07 2019-03-29 温州格蕾斯服饰有限公司 A kind of antibacterial garment and its manufacture craft
CN109736075A (en) * 2018-12-28 2019-05-10 杭州蓝色倾情服饰有限公司 Uvioresistant fabrics and preparation method thereof
CN111567956A (en) * 2020-05-29 2020-08-25 邦威防护科技股份有限公司 Medical protective clothing
CN112878066A (en) * 2021-01-19 2021-06-01 绍兴佳卓新材料科技有限公司 Antibacterial corrosion-resistant anti-scaling food-grade nano composite coating and preparation method thereof
CN113174749A (en) * 2021-04-20 2021-07-27 红豆集团无锡红豆童装有限公司 Ultra-light organic cotton textile fabric and preparation method thereof

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Application publication date: 20180420