CN107858831B - Preparation method of water-absorbing and breathable fabric - Google Patents

Preparation method of water-absorbing and breathable fabric Download PDF

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CN107858831B
CN107858831B CN201710915817.5A CN201710915817A CN107858831B CN 107858831 B CN107858831 B CN 107858831B CN 201710915817 A CN201710915817 A CN 201710915817A CN 107858831 B CN107858831 B CN 107858831B
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water
cotton yarn
fabric
parts
yarn
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CN107858831A (en
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杨艳
叶力
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NINGBO BOYANG HOME TEXTILE GROUP Co.,Ltd.
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Ningbo Boyang Home Textile Group Co ltd
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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
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/15Proteins or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/37Mixtures of compounds all of which are anionic
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3719Polyamides or polyimides
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    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
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    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D13/00Woven fabrics characterised by the special disposition of the warp or weft threads, e.g. with curved weft threads, with discontinuous warp threads, with diagonal warp or weft
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    • D03WEAVING
    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D15/00Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
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    • 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
    • D06M10/04Physical treatment combined with treatment with chemical compounds or elements
    • D06M10/08Organic compounds
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    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/144Alcohols; Metal alcoholates
    • D06M13/148Polyalcohols, e.g. glycerol or glucose
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    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
    • D06M15/05Cellulose or derivatives thereof
    • D06M15/09Cellulose ethers
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    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
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    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
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    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/10Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
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    • D06M2200/20Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease
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    • D10B2201/02Cotton
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    • D10B2331/00Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
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Abstract

The invention discloses a method for manufacturing a water-absorbing breathable fabric, which comprises the following specific steps: putting the cotton yarn into a detergent solution for treatment, cleaning and airing; putting the pretreated cotton yarn into a plasma treatment tank for plasma treatment, then treating with a post-treatment agent, cleaning and drying to obtain modified cotton yarn; and (3) interweaving modified cotton yarns serving as warps and blended yarns serving as wefts to obtain base cloth, and performing heat setting and finishing to obtain the water-absorbing breathable fabric. The beneficial effects are that: the preparation method improves the additional value of the cotton fiber yarn, has simple preparation method, convenient operation and control, stable quality and high production efficiency, and is easy for large-scale industrial production; the fabric obtained by the preparation method has excellent water absorption and air permeability, and can keep a human body in a constant-temperature, dry and comfortable state all the time; the fabric can form a unique warm-keeping system, the warm-keeping performance is improved, and the fabric has no stimulation to skin, soft hand feeling, good glossiness and strong dyeing property.

Description

Preparation method of water-absorbing and breathable fabric
Technical Field
The invention relates to the field of garment materials, in particular to a preparation method of a water-absorbing breathable fabric.
Background
With the progress of scientific and technological technology and the improvement of life quality of people, the consumption idea of wearing clothes is changed into health and comfort, so that the water absorption and air permeability of the fabric are one of the performances of ideal clothes fabrics, and the fabric becomes a hot point of common attention of consumers and manufacturers. The garment fabric with water absorption and air permeability can absorb moisture and sweat emitted by a human body to the maximum extent, and quickly transmit and diffuse the moisture and sweat, so that the skin is kept clean and dry, and the wearing comfort performance of the garment is improved. Particularly, under the weather conditions of high temperature and high humidity in summer, a large amount of sweat can be produced when people take strenuous exercise, so that the sweat on the surface of the skin is difficult to discharge, and the stuffy feeling is caused; when the human body stops sweating, the fabric is slower in moisture release, and the moisture in the fabric squeezes away the air in the fabric, so that the heat preservation of the fabric is reduced, the skin surface is wet and cold, and the wearing comfort of the fabric is greatly reduced. Therefore, garment materials with good water absorption and air permeability have become a common demand in the garment consumer market. It is well known that cotton fiber is an important natural fiber with a long history and has a place that other products cannot replace. In recent years, although cotton fibers are highly attractive because of their advantages such as good moisture absorption, soft hand, and comfortable wearing, they are significantly weaker than most chemical fibers in moisture permeability, and thus have limited application to high-performance fabrics such as water-absorbent and air-permeable fabrics. At present, most of researches on water-absorbing and air-permeable fabrics at home and abroad are focused on developing functional synthetic fibers and application of the developed functional synthetic fibers, most of the developed new fabrics are focused on synthetic fiber fabrics, and the researches on water-absorbing and air-permeable performances of pure natural fiber fabrics are less touched.
In the prior art, as a chinese patent with an issued publication number of CN 104118162B, a water-absorbing breathable fabric is disclosed, which comprises a fabric body woven by warps and wefts to form a plain weave structure, wherein the warps are hollow PET polyester filaments, the surface of the PET polyester filaments is provided with a plurality of through holes communicated to the hollow cavities inside the PET polyester filaments, zeolite particles are embedded in the wall body of the PET polyester filaments, the wefts are bamboo fiber filaments, and the side portions of the bamboo fiber filaments are provided with a plurality of grooves extending along the extending direction of the bamboo fiber filaments. The fabric has good water absorption and air permeability, can ensure that water attached to the surface of warp threads is quickly absorbed into the fibers to keep the human body fresh and comfortable, but the fabric has insufficient softness and insufficient wearing comfort.
Disclosure of Invention
The invention aims to provide the preparation method of the water-absorbing and breathable fabric, which is simple in preparation method, convenient to operate and control, stable in quality, excellent in water-absorbing and breathability, free of stimulation to skin, soft in hand feeling and good in warmth retention, and can improve the additional value of cotton fiber yarns.
Aiming at the problems mentioned in the technology, the invention adopts the technical scheme that:
the manufacturing method of the water-absorbing breathable fabric comprises the steps of cotton yarn pretreatment, modified cotton yarn preparation and water-absorbing breathable fabric preparation, and comprises the following specific steps:
pretreatment of cotton yarn: putting cotton yarn into a detergent solution with a bath ratio of L:48-53 and a concentration of 0.9-1.1g/L, treating for 20-40min at 90-100 ℃, then cleaning with clear water, airing for later use, wherein the detergent is a mixture of sodium dodecyl benzene sulfonate, ramibane A and antibacterial protein with a weight ratio of 1:0.33-0.36:0.02-0.022, the amino acid sequence of the antibacterial protein is TDHKLCVYLCRVLHPGKLCVCVNCSKQDNAYASAICHGGKTCEGICADATATMDRYSDTGGPLSTARCVNAFHFYKGCSLYEENVSYKPFVVSWKYGVAGFYTHCGPNFCCCIS, the antibacterial protein can be adsorbed on the surface of bacteria through the action of electric charges, the osmotic pressure of the bacteria is changed, active substances in the bacteria are released, the bacteria are killed, bacterial substances in the cotton fiber are killed, meanwhile, the antibacterial protein has hydrophilic groups, can destroy cell walls in the cotton fiber, enter the cotton fiber, kill the bacteria in the cotton fiber, and release impurities in the cotton fiber at the same time, the components of the detergent can cooperate with each other, so that the surface tension and wetting, penetrating and emulsifying properties of water are greatly reduced, the detergent has better degreasing, decontamination and sterilization capabilities, and impurities such as dirt, grease and the like on cotton yarns can be thoroughly removed;
preparing modified cotton yarns: putting the pretreated cotton yarn into a low-temperature plasma processor, performing plasma treatment for 80-100s under the power of 130-160w, immersing the cotton yarn into a post-treatment agent with the bath ratio of 1:50-70, wherein the post-treatment agent comprises methyltriethoxysilane and dimethyldiethoxysilane with the weight ratio of 1:0.021-0.025, performing post-treatment for 20-40min at 95-105 ℃, taking out the yarn, cleaning the yarn with absolute ethyl alcohol and distilled water, and drying to obtain the modified cotton yarn, wherein charged energy particles in the plasma can impact the surface of the cotton yarn to cause etching, so that the surface of the cotton yarn generates etching effect and a large number of free radicals, and a methyltriethoxysilane hydrophobic group can be grafted to the surface of the cotton yarn fiber to form a Si-O-Si or Si-C structure, so that the surface of the cotton yarn fiber has hydrophobicity, the interior of the cotton yarn fiber still keeps the hydrophilic state of the original cotton yarn, and the modified veil fiber has good mechanical strength, thermal stability and chemical stability;
preparing the water-absorbing and air-permeable fabric: modified cotton yarn is used as warp, blended yarn is used as weft, the warp and the weft are interwoven by adopting a top-to-bottom plain weave to obtain base cloth, the base cloth is subjected to heat setting, and finally the base cloth is put into finishing liquid for finishing to obtain the water-absorbing and air-permeable fabric, the preparation method of the water-absorbing and air-permeable fabric is characterized in that the weight ratio of modified hollow polyester fiber to hollow viscose fiber in the mixed yarn is 1:0.35-0.38, hydrophilic groups are introduced into molecules of the modified hollow polyester fiber, the hydrophilic state of the surface of the fiber can be automatically adjusted, so that the wetting and diffusion speed of water on the surface of the fiber is accelerated, and multiple capillaries are formed between the hollow structure of the fiber and a fiber aggregate in the fabric to form an excellent moisture-conducting system, the moisture-conducting performance of the fabric is remarkably improved, the moisture and the sweat on the skin are rapidly transported away, and the: 2-3 parts of water-soluble polyurethane, 19-22 parts of propylene glycol, 2-3 parts of silk fibroin, 2-3 parts of fatty alcohol-polyoxyethylene ether, 0.5-1 part of fatty alcohol-polyethylene glycol ester, 1-2 parts of hydroxypropyl methyl cellulose, 1-2 parts of emulsifier and 120 parts of 100 parts of water, wherein the finishing liquid has good synergistic interaction effect, can be subjected to crosslinking reaction with groups in fibers, effectively keeps the molecules of fiber polymer chains connected with each other, enables the molecules on the chains to be kept at opposite positions, improves the crease resistance of the fabric, can improve the dyeing property, whiteness, strength, luster and softness of the fabric, has excellent water absorption and air permeability, can enable a human body to be in a heat-moisture balance state all the time, further enables the human body to be kept in a constant-temperature, dry and comfortable state all the time, and contains more still air, a unique warm-keeping system is formed, the warm-keeping performance of the fabric is improved, and in addition, the fabric has no stimulation effect on skin, soft hand feeling, good glossiness and strong dyeing property.
Compared with the prior art, the invention has the advantages that: the preparation method improves the additional value of the cotton fiber yarn, has simple preparation method, convenient operation and control, stable quality and high production efficiency, and is easy for large-scale industrial production; the fabric obtained by the preparation method has excellent water absorption and air permeability, and the clothes prepared by the fabric can enable the human body to be in a heat-humidity balance state all the time, so that the human body is kept in a constant-temperature, dry and comfortable state all the time; the fabric contains more static air, forms a unique warm-keeping system, increases the warm-keeping performance of the fabric, and has no stimulation to skin, soft hand feeling, good glossiness and strong dyeability; the fabric can effectively keep the molecules of fiber polymer chains connected with each other, so that the molecules on the chains can be kept at opposite positions, and the crease resistance of the fabric is improved; the surface of the cotton yarn fiber has hydrophobicity, the interior of the cotton yarn fiber still keeps the hydrophilic state of the original cotton yarn, and the modified veil fiber has good mechanical strength, thermal stability and chemical stability.
Detailed Description
The scheme of the invention is further illustrated by the following examples:
example 1:
the manufacturing method of the water-absorbing breathable fabric comprises the steps of cotton yarn pretreatment, modified cotton yarn preparation and water-absorbing breathable fabric preparation, and comprises the following specific steps:
1) pretreatment of cotton yarn: putting cotton yarn into a detergent solution with a bath ratio of L:48 and a concentration of 1.1g/L, treating for 36min at 92 ℃, then cleaning with clear water, and airing for later use, wherein the detergent is a mixture of sodium dodecyl benzene sulfonate, ramibanum A and antibacterial protein with a weight ratio of 1:0.33:0.022, the amino acid sequence of the antibacterial protein is TDHKLCVYLCRVLHPGKLCVCVNCSKQDNAYASAICHGGKTCEGICADATATMDRYSDTGGPLSTARCVNAFHFYKGCSLYEENVSYKPFVVSWKYGVAGFYTHCGPNFCCCIS, the antibacterial protein can be adsorbed on the surface of bacteria through charge action to change the osmotic pressure of the bacteria, so that active substances in the bacteria are released to finally cause the death of the bacteria and kill bacterial substances in the cotton fibers, meanwhile, the antibacterial protein has hydrophilic groups which can damage cell walls in the cotton fibers, enter the cotton fibers, kill the bacteria in the cotton fibers and release impurities in the cotton fibers, and the components of the detergent can cooperate with one another to greatly reduce the surface tension and wetting of water, The cotton yarn has the advantages of good penetrating and emulsifying properties, good degreasing, decontamination and sterilization capabilities, and capability of thoroughly removing impurities such as dirt, grease and the like on cotton yarns;
2) preparing modified cotton yarns: putting the pretreated cotton yarn into a low-temperature plasma processor, performing plasma processing for 100s under the power of 135w, immersing the cotton yarn into a post-processing agent with the bath ratio of 1:52, wherein the post-processing agent comprises methyltriethoxysilane and dimethyldiethoxysilane with the weight ratio of 1:0.025, performing post-processing for 40min at the temperature of 95 ℃, taking out the yarn, cleaning the yarn with absolute ethyl alcohol and distilled water, and drying to obtain the modified cotton yarn, wherein charged particles in the plasma can impact the surface of the cotton yarn to cause etching, then the surface of the cotton yarn generates etching effect and generates a large number of free radicals, and a methyltriethoxysilane hydrophobic group can be grafted to the surface of the cotton yarn fiber to form a Si-O-Si or Si-C structure, so that the surface of the cotton yarn fiber has hydrophobicity, and the interior of the cotton yarn fiber still keeps the hydrophilic state of the original cotton yarn, in addition, the modified veil fiber has good mechanical strength, thermal stability and chemical stability;
3) preparing the water-absorbing and air-permeable fabric: modified cotton yarn is used as warp, blended yarn is used as weft, the warp and the weft are interwoven by adopting a top-to-bottom plain weave to obtain base cloth, the base cloth is subjected to heat setting, and finally the base cloth is put into finishing liquid for finishing to obtain the water-absorbing and air-permeable fabric, the weight ratio of modified hollow polyester fiber to hollow viscose fiber in the blended yarn is 1:0.38, hydrophilic groups are introduced into molecules of the modified hollow polyester fiber, the hydrophilic state of the fiber surface can be automatically adjusted, the wetting and diffusion speed of water on the fiber surface is accelerated, multiple capillaries are formed between the hollow structure of the fiber and a fiber aggregate in the fabric to form an excellent moisture-conducting system, the moisture-conducting property of the fabric is remarkably improved, moisture and sweat on the skin are rapidly transported away, and the finishing liquid comprises the following components in parts by weight: 2 parts of water-soluble polyurethane, 22 parts of propylene glycol, 2 parts of silk fibroin, 3 parts of fatty alcohol-polyoxyethylene ether, 0.5 part of fatty alcohol-polyethylene glycol ester, 2 parts of hydroxypropyl methyl cellulose, 1.1 parts of emulsifier and 120 parts of water, wherein the finishing liquid has good synergy among the components, can perform cross-linking reaction with groups in fibers, effectively keeps the molecules of fiber polymer chains connected with each other, enables the molecules on the chains to be kept at opposite positions, improves the crease resistance of the fabric, can improve the dyeing property, whiteness, strength, luster and softness of the fabric, has excellent water absorption and air permeability, can enable a human body to be always in a heat-moisture balance state by the clothing prepared from the fabric, further enables the human body to be always kept in a constant-temperature, dry and comfortable state, and simultaneously contains more static air, forms a unique heat preservation system, and increases the heat preservation performance of the fabric, in addition, the fabric has no stimulation to skin, soft hand feeling, good glossiness and strong dyeability.
Example 2:
the manufacturing method of the water-absorbing breathable fabric comprises the following specific steps:
1) pretreatment of cotton yarn: putting the cotton yarn into a detergent solution with a bath ratio of L:53 and a concentration of 0.9g/L, treating for 20min at 100 ℃, then cleaning with clear water, and airing for later use, wherein the detergent is a mixture of sodium dodecyl benzene sulfonate, ramination A and antibacterial protein in a weight ratio of 1:0.36:0.02, and the amino acid sequence of the antibacterial protein is TDHKLCVYLCRVLHPGKLCVCVNCSKQDNAYASAICHGGKTCEGICADATATMDRYSDTGGPLSTARCVNAFHFYKGCSLYEENVSYKPFVVSWKYGVAGFYTHCGPNFCCCIS;
2) preparing modified cotton yarns: putting the pretreated cotton yarn into a low-temperature plasma processor, performing plasma processing for 80s at the power of 160w, immersing the cotton yarn into a post-processing agent with the bath ratio of 1:70, performing post-processing for 20min at the temperature of 105 ℃, taking out the yarn, cleaning the yarn with absolute ethyl alcohol and distilled water, and drying to obtain the modified cotton yarn;
3) the modified cotton yarn is used as warp, the blended yarn is used as weft, the warp and the weft are interwoven by adopting a one-over-one-under plain weave to obtain base cloth, the base cloth is subjected to heat setting, and finally the base cloth is put into finishing liquid for finishing to obtain the water-absorbing and air-permeable fabric, the preparation method of the water-absorbing and air-permeable fabric comprises the steps of putting 3 parts of water-soluble polyurethane, 20 parts of propylene glycol, 3 parts of silk fibroin, 2.2 parts of fatty alcohol polyoxyethylene ether, 1 part of fatty alcohol polyglycol ester, 1.1 parts of hydroxypropyl methyl cellulose, 1.7 parts of emulsifier and 105 parts of water for finishing to obtain the water-absorbing and air-permeable fabric, wherein the weight ratio of the modified hollow polyester fiber to the hollow viscose fiber in the blended yarn is 1: 0.35.
Example 3:
the manufacturing method of the water-absorbing breathable fabric comprises the following steps:
putting the cotton yarn into a detergent solution with a bath ratio of L:50 and a concentration of 1g/L, treating for 30min at 96 ℃, then cleaning with clear water, and airing for later use, wherein the detergent is a mixture of sodium dodecyl benzene sulfonate, ramination A and antibacterial protein in a weight ratio of 1:0.35:0.021, and the amino acid sequence of the antibacterial protein is TDHKLCVYLCRVLHPGKLCVCVNCSKQDNAYASAICHGGKTCEGICADATATMDRYSDTGGPLSTARCVNAFHFYKGCSLYEENVSYKPFVVSWKYGVAGFYTHCGPNFCCCIS;
putting the pretreated cotton yarn into a low-temperature plasma processor, performing plasma processing for 90s under the power of 150w, immersing the cotton yarn into a post-processing agent with the bath ratio of 1:60, performing post-processing on the cotton yarn for 30min at the temperature of 100 ℃, taking out the cotton yarn, cleaning the cotton yarn with absolute ethyl alcohol and distilled water, and drying to obtain the modified cotton yarn;
the modified cotton yarn is used as warp, the blended yarn is used as weft, the warp and the weft are interwoven by adopting a one-over-one-under plain weave to obtain base cloth, the base cloth is subjected to heat setting, and finally the base cloth is put into finishing liquid containing 2.5 parts of water-soluble polyurethane, 20 parts of propylene glycol, 2.5 parts of silk fibroin, 2.5 parts of fatty alcohol-polyoxyethylene ether, 0.7 part of fatty alcohol-polyethylene glycol ester, 1.6 parts of hydroxypropyl methyl cellulose, 1.4 parts of emulsifier and 110 parts of water for finishing to obtain the water-absorbing and air-permeable fabric, wherein the weight ratio of the modified hollow polyester fiber to the hollow viscose fiber in the blended yarn is 1: 0.36.
Example 4:
and (3) testing the performance of the water-absorbing breathable fabric:
the cooling sensation test was performed on the fabrics of example 1, example 2 and example 3 as a test group, a normal commercially available cotton-containing fabric as a control group 1, and a normal commercially available water-absorbent and breathable fabric as a control group 2.
Sweat absorption test: preparing sweat according to GB/T14576 + 2009 color fastness test light and sweat composite color fastness, putting the fabric to be tested in the sweat, completely wetting for 5min, taking out and naturally hanging, when the time interval of two drops of water falling exceeds 30s, considering that the sample does not drip any more, immediately weighing the sample, and calculating the sweat absorption rate of the fabric, wherein the result is shown in Table 1.
And (3) testing air permeability: the test was carried out with reference to GB/T5453-1997 determination of the air permeability of textile fabrics.
Table 1: sweat absorption and air permeability test results
Figure DEST_PATH_IMAGE002
As can be seen from Table 1, the fabrics of example 1, example 2 and example 3 of the present invention have higher values of sweat absorption and air permeability than those of control group 1 and control group 2, which shows that the water-absorbing and air-permeable fabrics prepared by the preparation method of the present invention have better sweat absorption and air permeability.
Conventional operations in the operation steps of the present invention are well known to those skilled in the art and will not be described herein.
The embodiments described above are intended to illustrate the technical solutions of the present invention in detail, and it should be understood that the above-mentioned embodiments are only specific embodiments of the present invention, and are not intended to limit the present invention, and any modification, supplement or similar substitution made within the scope of the principles of the present invention should be included in the protection scope of the present invention.
Sequence listing
<110> Chuanda general electronic science and technology Co., Ltd in Ningbo northern Lang
Preparation method of <120> water-absorbing and air-permeable fabric
<160> 1
<170> SIPOSequenceListing 1.0
<210> 1
<211> 114
<212> PRT
<213> Artificial Synthesis (Mytilus corescuus)
<400> 1
Thr Asp His Lys Leu Cys Val Tyr Leu Cys Arg Val Leu His Pro Gly
1 5 10 15
Lys Leu Cys Val Cys Val Asn Cys Ser Lys Gln Asp Asn Ala Tyr Ala
20 25 30
Ser Ala Ile Cys His Gly Gly Lys Thr Cys Glu Gly Ile Cys Ala Asp
35 40 45
Ala Thr Ala Thr Met Asp Arg Tyr Ser Asp Thr Gly Gly Pro Leu Ser
50 55 60
Thr Ala Arg Cys Val Asn Ala Phe His Phe Tyr Lys Gly Cys Ser Leu
65 70 75 80
Tyr Glu Glu Asn Val Ser Tyr Lys Pro Phe Val Val Ser Trp Lys Tyr
85 90 95
Gly Val Ala Gly Phe Tyr Thr His Cys Gly Pro Asn Phe Cys Cys Cys
100 105 110
Ile Ser

Claims (2)

1. The preparation method of the water-absorbing breathable fabric comprises the following steps:
pretreatment of cotton yarn: putting the cotton yarn into a detergent solution with a bath ratio of L:48-53 and a concentration of 0.9-1.1g/L, treating at 90-100 ℃ for 20-40min, then washing with clear water, and airing for later use, wherein the detergent concentration in the step of pretreating the cotton yarn is 0.9-1.1g/L, and the detergent is a mixture of sodium dodecyl benzene sulfonate, ramination A and bacteriostatic protein in a weight ratio of 1:0.33-0.36: 0.02-0.022;
preparing modified cotton yarns: putting the pretreated cotton yarn into a low-temperature plasma processor, performing plasma treatment for 80-100s under the power of 130-160W, immersing the cotton yarn into a post-treatment agent with the bath ratio of 1:50-70, performing post-treatment for 20-40min at the temperature of 95-105 ℃, taking out the yarn, cleaning the yarn with absolute ethyl alcohol and distilled water, and drying to obtain the modified cotton yarn, wherein the post-treatment agent comprises methyltriethoxysilane and dimethyldiethoxysilane with the weight ratio of 1: 0.021-0.025;
preparing the water-absorbing and air-permeable fabric: the modified cotton yarn is used as warp, the mixed yarn of the modified hollow polyester fiber and the hollow viscose fiber with the weight ratio of 1:0.35-0.38 is used as weft, hydrophilic groups are introduced into molecules of the modified hollow polyester fiber, the warp and the weft are interwoven by adopting an upper plain weave and a lower plain weave to obtain base cloth, the base cloth is subjected to heat setting, and finally the base cloth is put into finishing liquid for finishing, so that the water-absorbing and breathable fabric is obtained.
2. The method for preparing the water-absorbing breathable fabric according to claim 1, characterized in that: the finishing liquid in the preparation step of the water-absorbing breathable fabric comprises the following components in parts by weight: 2-3 parts of water-soluble polyurethane, 19-22 parts of propylene glycol, 2-3 parts of silk fibroin, 2-3 parts of fatty alcohol-polyoxyethylene ether, 0.5-1 part of fatty alcohol-polyethylene glycol ester, 1-2 parts of hydroxypropyl methyl cellulose, 1-2 parts of an emulsifier and 120 parts of 100-fold water.
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