CN106012495B - A kind of linen and preparation method thereof with safeguard function - Google Patents

A kind of linen and preparation method thereof with safeguard function Download PDF

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CN106012495B
CN106012495B CN201610528511.XA CN201610528511A CN106012495B CN 106012495 B CN106012495 B CN 106012495B CN 201610528511 A CN201610528511 A CN 201610528511A CN 106012495 B CN106012495 B CN 106012495B
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linen
preparation
chitosan
acid solution
washing
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CN106012495A (en
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王浩
张晓丽
杜兆芳
刘陶
刘娜
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Anhui Agricultural University AHAU
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Anhui Agricultural University AHAU
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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
    • D06M11/32Treating 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
    • D06M11/38Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
    • 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
    • D06M11/07Treating 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 halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof
    • D06M11/30Treating 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 halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof with oxides of halogens, oxyacids of halogens or their salts, e.g. with perchlorates
    • 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
    • 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
    • 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
    • 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
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/188Monocarboxylic acids; Anhydrides, halides or salts thereof
    • 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
    • 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
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • 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
    • D06M15/03Polysaccharides or derivatives thereof
    • 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
    • D06M16/00Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
    • 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
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/20Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease
    • 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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
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  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

The invention discloses a kind of linen and preparation method thereof with safeguard function,It include the pretreatment of linen,Oxidation processes,The preparation of chitosan acetic acid solution,The preparation of chitin modified oxidation linen and tea polyphenols are to preparation processes such as the composite finishings of chitin modified linen,The present invention uses periodic acid or periodate to be selectively oxidized linen first,Imidization can be occurred with the chitosan containing NH2 by generating active group aldehyde radical CHO,Under conditions of without using any crosslinking agent or other chemical addition agents,The two produces chemical bonding,Fabric is enhanced during postorder arranges to the adsorption capacities of tea polyphenols,Promote the combination of tea polyphenols and linen,Tea polyphenols finishing functions process is avoided to use other reagents,The product of the present invention has good antibacterial,Crease-resistant and uvioresistant etc. is multi-functional;The preparation process of the product is simple, easy to operate, and cleanly production is also achieved in preparation process, meets the requirement of ecological textile.

Description

A kind of linen and preparation method thereof with safeguard function
Technical field
The present invention relates to a kind of method of modifying of linen, more particularly to one kind to have antibacterial, crease-resistant, uvioresistant etc. more The processing method of functional linen.
Background technology
Flaxen fiber is native cellulose fibre, has the characteristics that recyclability, biodegradability and nontoxic and pollution-free. Flaxen fiber is widely used in clothes, household and industry with its graceful gloss, good humidity absorption and release and natural antibacterial With etc. textile fields.But there is the shortcomings of creasing easily, size is unstable in flaxen fiber;And when wearing summer, linen Ultraviolet resistance also needs to further increase.As new varieties, high-performance and multi-functional textile fiber material continuously emerge, Requirement objectively to flaxen fiber and its product is also higher and higher.The multifunction of exploitation flaxen fiber and its product is modified and carries Its high added value and performance have become a general orientation of people's research.
Since the functional finishing agent developed at present is attached to flaxen fiber and its product surface by physical absorption mostly, still The two combines insecure.Therefore it during flaxen fiber tradition is modified, needs using chemical cross-linking agent (resin, glyoxal, organosilicon and more First carboxylic acid etc.) or coupling agent " bridging " effect its functional finishing agent is grafted on flaxen fiber, to reach improvement flaxen fiber Performance and the purpose for assigning its function durability.However, flaxen fiber product tradition is modified, there are certain drawbacks, such as resin or second two Aldehyde can make to remain and release formaldehyde on linen after arranging, and larger harm is generated to human body;And crosslinking agent or coupling agent grafting Modified flaxen fiber surface has inevitably been crosslinked one layer of chemical substance, affects the good characteristic of natural ramie fiber, and right Health has a negative impact.Therefore, traditional modification technology is while assigning flaxen fiber cellulose fiber product function, to life The harm of state environmental and human health impacts is serious, it is difficult to meet ecological, multi-functional and persistent multiple requesting.
Tealeaves is the abundant natural plant resource in China, and tea polyphenols are more than the 30 kinds of phenol separated and extracted from tealeaves again The complex of class compound, predominantly flavanols (catechin) class, accounts for the 60~80% of total amount.Tea polyphenols are special due to its Ingredient and structure have many unique physiological activity, such as excellent oxidation resistance, radioresistance, anti-inflammation and sterilization, uvioresistant Etc. functions, be widely used in the fields such as medicines and health protection, food processing, daily-use chemical industry, fine chemistry industry at present.Recent year Outer researcher has carried out certain research using tea polyphenols as natural dye for textile dyeing and functional treatment, and tea is more The modification of phenol can not only make fabric have unique color and luster, can also impart to many natural healthcare functions of fabric.But The binding strength using chemical cross-linking agent or mordant enhancing tea polyphenols and fiber, meeting are usually needed in tea polyphenols dyeing and finishing process It has a negative impact to environment or health, thus limits the application of tea polyphenols on the textile.
Chitosan is the deacetylated product of chitin, is unique alkaline polysaccharide in nature.Chitosan have it is nontoxic, The excellent performances such as tasteless and good biological degradability, recyclability, Antimicrobial preservative, film forming.In order to realize chitosan and Application of the two kinds of natural macromolecular materials of tea polyphenols in the modification of flaxen fiber multifunction, the present invention is using linen through periodic acid Or after periodate selective oxidation, then through chitosan and tea polyphenols ecology composite finishing technology, its product is set to have good The multifunctionalities such as antibacterial, wrinkle resistant, antiultraviolet, and there is good function durability.The finishing functions process is without using any Crosslinking agent or metal salt mordant, and the finishing agent asepsis environment-protecting used, realize cleanly production, meet wanting for ecological textile It asks.The present invention prepares the method for function linen there is not yet appointing jointly using Adsorption of Tea Polyphenols after chitin modified oxidation linen What is reported.The purpose of the present invention is to provide one kind having the multi-functional linen such as durable antibiotic, wrinkle resistant and antiultraviolet, Include the hemp fabrics such as ramie, flax, jute.With general linen it is function modified compared with, using chitin modified oxygen The method of Adsorption of Tea Polyphenols carries out linen function modified after change linen, meets ecological, multi-functional and lasting Property multiple requesting, and method is simple, safety.
Invention content
It is an object of the invention to overcome the deficiencies of the prior art and provide provide it is a kind of have durable antibiotic, it is wrinkle resistant with And the multi-functional linen such as antiultraviolet, it is had a single function with solving linen in the prior art, function modified product harm The larger technical problem of property.
The present invention is achieved by the following technical solutions:The invention discloses a kind of systems with safeguard function linen Preparation Method, including following preparation process:
1) pretreatment of linen:Linen is added in alkaline solution, after stirring at room temperature, washing, then by hemp Object, which is put into acid solution, to be impregnated, then is washed, and alkalization linen is obtained after drying;
2) oxidation processes of linen:By the alkalization linen obtained in prepared periodic acid and step 1) by bath raio 50:1 is mixed, and is protected from light under 40~60 DEG C of water bath conditions, after reaction, linen is taken out and is washed, first Linen after washing is placed in glycerin solution and is impregnated, then puts it into deionized water and impregnates again, after washing is dried It is spare up to oxidation linen;
3) preparation of chitosan acetic acid solution:It adds chitosan into acetic acid solution and is dissolved, prepare chitosan second Acid solution, wherein the mass concentration of chitosan is 0.5~4% in the chitosan acetic acid solution;
4) preparation of chitin modified oxidation linen:It will be in the chitosan acetic acid solution and step 2) prepared in step 3) Obtained oxidation linen is by bath raio 50:1 is mixed, and after infiltration, 1~2h is persistently stirred under water bath condition, then by hemp Object washing, which is placed in baking oven, is dried, and is finally washed up to chitin modified oxidation linen after drying, spare;
5) composite finishing of the tea polyphenols to chitin modified linen:The chitin modified oxidation fiber crops that will be prepared in step 4) Fabric presses bath raio 1:50 put into tea polyphenols solution, and 1~1.5h is persistently stirred under heating, are then placed on linen washing It is dried in baking oven, the rear linen up to composite finishing finally is dried into linen washing.
Further, since flaxen fiber has higher crystallinity, alkali pre-activate reaction is carried out before carrying out oxidation reaction, Be conducive to the raising of postorder efficiency, so step 1) neutral and alkali solution is the sodium hydroxide solution of 15~25wt%, Acid solution is the acetic acid solution that mass concentration is 5~10%, and the time stirred at room temperature is 20~60min.
Further, the present invention is selectively oxidized linen using periodic acid, generates new active group aldehyde radical- CHO makes cellulose imidization can occur with the chitosan containing-NH2.A concentration of 2 of periodic acid described in step 2)~ 10g/L, the 0.5~3h of time being protected from light can also be selectively oxidized using a concentration of 2~10g/L periodates;Step It is rapid 2) in also first the linen after washing can be placed in acetone soln impregnate, then put it into deionized water and impregnate again.
Further, in order to dissolve completely chitosan, acetic acid solution described in step 3) is volumetric concentration For 1~4% acetic acid solution.
Further, in order not to the surface texture for destroying linen and preferably modified, the temperature of water-bath in step 4) Be 40~60 DEG C, the linen after washing be placed in baking oven first 5~10min of preliminary drying under the conditions of 80 DEG C, then 140~ 160 DEG C bake 3min, then again dry linen washing.
Further, in order to preferably carry out composite finishing to modified linen, the concentration of tea polyphenols solution in step 5) Temperature for 6~20g/L, heating is 60~90 DEG C, and the linen after washing is placed in baking oven the first preliminary drying 5 under the conditions of 80 DEG C Then~10min bakes 3min at 140~160 DEG C, the rear linen up to composite finishing finally is dried in linen washing.
Further, in order to be suitable for more linens, the type of linen can be in ramie, flax or jute It is any.
Further, it since the present invention first uses periodic acid or periodate to be selectively oxidized linen, generates New active group aldehyde radical-CHO makes cellulose imidization can occur with the chitosan containing-NH2, without using any friendship Under conditions of joining agent or other chemical addition agents, chemical bonding is produced between the two, chitosan is made to anchor at hemp securely Object surface.And fabric is more to tea during the hydroxyl contained in chitosan molecule and free amino are conducive to enhancing postorder arrangement The adsorption capacity of phenol promotes the binding strength of tea polyphenols and linen, and to avoid, tea polyphenols dye or finishing functions process makes With any crosslinking agent or metal salt mordant, in order to preferably carry out composite finishing, the deacetylation of the chitosan is 80 ~95%.
The present invention uses resourceful chitosan and natural plant extracts tea polyphenols as finishing agent, whole with ecology Reason technology improves the multifunctionality of ramie product, increases its added value.The present invention uses periodic acid or periodate to fiber crops first Fabric is selectively oxidized, and generates new active group aldehyde radical-CHO, makes cellulose that can occur with the chitosan containing-NH2 sub- Aminating reaction produces chemical bonding, makes between the two under conditions of without using any crosslinking agent or other chemical addition agents Chitosan anchors at linen surface securely.And after the hydroxyl contained in chitosan molecule and free amino are conducive to enhancing Fabric promotes the binding strength of tea polyphenols and linen, to avoid tea more to the adsorption capacity of tea polyphenols during sequence arranges Phenol dyes or finishing functions process uses any crosslinking agent or metal salt mordant.The present invention has durable antibiotic, wrinkle resistant and anti-purple The multi-functionals such as outside line, including hemp fabrics such as ramie, flax, jutes.With general linen it is function modified compared with, Linen is carried out function modified using the method for Adsorption of Tea Polyphenols after chitin modified oxidation linen, meets ecology Property, multifunctionality and persistent multiple requesting, and method is simple, safety.
Description of the drawings
Fig. 1 is the infrared spectrum analysis spectrogram of ramie fabric before and after the processing.
Specific implementation mode
It elaborates below to the embodiment of the present invention, the present embodiment is carried out lower based on the technical solution of the present invention Implement, gives detailed embodiment and specific operating process, but protection scope of the present invention is not limited to following implementation Example.
Embodiment 1
Ramie fabric is added in the sodium hydroxide solution of 15wt%, 20min is stirred at room temperature, is washed 3 times, then 30min is impregnated in the glacial acetic acid that mass concentration is 5%, finally washing obtains alkalization ramie fabric after drying;
Compound concentration is that the sodium periodate solution of 2g/L is placed in brown conical flask, by 50:Above-mentioned be made is added in 1 bath raio Alkalization ramie fabric, be protected from light 0.5h in 40 DEG C of water-baths, obtain oxidation ramie fabric;Oxidation ramie fabric is taken out and is rinsed It is placed in glycerin solution and impregnates 2h, place into deionized water and impregnate for 24 hours.Finally washing obtains oxidation ramie and knits after drying Object;
The chitosan that the deacetylation weighed is 80% is added in the dilute acetic acid solutions that volumetric concentration is 1%, makes shell Glycan is dissolved completely in acetic acid solution, and the mass concentration of chitosan is 4% wherein in chitosan acetic acid solution;
The chitosan finishing liquid that the mass concentration of configuration is 4% is pressed into bath raio 50:1 is added oxidation ramie fabric, after infiltration 1h is persistently stirred at 40 DEG C, obtains modified ramie fabric;It is washed and is placed on 80 DEG C of preliminary drying 5min of baking oven, 140 DEG C bake 3min, finally washing obtain chitin modified oxidation ramie fabric after drying;
By bath raio 1:50 put into chitin modified oxidation ramie fabric in the tea polyphenols solution of a concentration of 6g/L, 60 1h is persistently stirred at DEG C, the ramie fabric that obtains that treated;It is washed and is placed on 80 DEG C of preliminary drying 5min of baking oven, 140 DEG C bake 3min, finally washing obtain the ramie fabric of composite finishing after drying.
Using GB/T 18830-2002《The evaluation of ultraviolet resistance of fabric》It is detected, measures the ultraviolet of fabric Line protection index (UPF values) is 42.4;Using GB/T 3819-1997《The measurement of textile fabric wrinkle recovery property》Into Row detection, the wrinkle angle recovery angle (warp-wise+broadwise) for measuring fabric reach 168 °;It is measured and is knitted by oscillation flask method quantitative experiment Object reaches 96.5% to the antibiotic rate of Escherichia coli, and the antibiotic rate of staphylococcus aureus reaches 98.6%.
Embodiment 2:
Sodolin is added in the sodium hydroxide solution of 25wt%, 60min is stirred at room temperature, is washed 5 times, then 30min is impregnated in the glacial acetic acid that mass concentration is 5%, finally washing obtains alkalization sodolin after drying;
Compound concentration is that the periodic acid solution of 10g/L is placed in brown conical flask, by 50:Above-mentioned be made is added in 1 bath raio Alkalization sodolin, be protected from light 3h in 60 DEG C of water-baths, obtain oxidation sodolin;Oxidation sodolin is taken out after rinsing It is placed in acetone soln and impregnates 2h, place into deionized water and impregnate for 24 hours.Finally washing obtains oxidation sodolin after drying;
It is that 95% chitosan is added in the dilute acetic acid solutions that volumetric concentration is 4% by the deacetylation weighed, keeps shell poly- Sugar is dissolved completely in acetic acid solution, and the mass concentration of chitosan is 0.5% wherein in chitosan acetic acid solution;
The chitosan finishing liquid that the mass concentration of configuration is 0.5% is pressed into bath raio 50:1 is added oxidation sodolin, infiltration 2h is persistently stirred at 60 DEG C afterwards, obtains modified sodolin;It is washed and is placed on 80 DEG C of preliminary drying 10min of baking oven, 150 DEG C of roastings 3min is dried, finally washing obtains chitin modified oxidation sodolin after drying;
By bath raio 1:50 put into chitin modified oxidation sodolin in the tea polyphenols solution of a concentration of 20g/L, 1.5h is persistently stirred at 90 DEG C, the sodolin that obtains that treated;It is washed and is placed on 80 DEG C of baking oven preliminary drying 5min, 150 DEG C 3min is baked, finally washing obtains the sodolin of composite finishing after drying.
Using GB/T 18830-2002《The evaluation of ultraviolet resistance of fabric》It is detected, measures the ultraviolet of fabric Line protection index (UPF values) is 45.6;Using GB/T 3819-1997《The measurement of textile fabric wrinkle recovery property》Into Row detection, the wrinkle angle recovery angle (warp-wise+broadwise) for measuring fabric reach 186.5 °;It is measured by vibrating flask method quantitative experiment Fabric reaches 97.9% to the antibiotic rate of Escherichia coli, and the antibiotic rate of staphylococcus aureus reaches 99.5%.
Embodiment 3:
Megila is added in the sodium hydroxide solution of 20wt%, 40min is stirred at room temperature, is washed 3 times, then 30min is impregnated in the glacial acetic acid that mass concentration is 5%, finally washing obtains alkalization megila after drying;
Compound concentration is that the sodium periodate solution of 8g/L is placed in brown conical flask, by 50:Above-mentioned be made is added in 1 bath raio Alkalization megila, be protected from light 2h in 50 DEG C of water-baths, obtain oxidation megila;Oxidation megila is taken out after rinsing It is placed in acetone soln and impregnates 2h, place into deionized water and impregnate for 24 hours.Finally washing obtains oxidation megila after drying;
It is that 85% chitosan is added in the dilute acetic acid solutions that volumetric concentration is 1% by the deacetylation weighed, keeps shell poly- Sugar is dissolved completely in acetic acid solution, and the mass concentration of chitosan is 4% wherein in chitosan acetic acid solution;
It is that 4% chitosan finishing liquid presses bath raio 50 by the mass concentration of configuration:1 be added oxidation megila, after infiltration 1h is persistently stirred at 60 DEG C, obtains modified megila;It is washed and is placed on 80 DEG C of preliminary drying 10min of baking oven, 160 DEG C bake 3min, finally washing obtain chitin modified oxidation megila after drying;
By bath raio 1:50 put into chitin modified oxidation megila in the tea polyphenols solution of a concentration of 15g/L, 1h is persistently stirred at 70 DEG C, the megila that obtains that treated;It is washed and is placed on 80 DEG C of preliminary drying 5min of baking oven, 150 DEG C of roastings 3min is dried, finally washing obtains the megila of composite finishing after drying.
Using GB/T 18830-2002《The evaluation of ultraviolet resistance of fabric》It is detected, measures the ultraviolet of fabric Line protection index (UPF values) is 50.4;Using GB/T 3819-1997《The measurement of textile fabric wrinkle recovery property》Into Row detection, the wrinkle angle recovery angle (warp-wise+broadwise) for measuring fabric reach 177.5 °;It is measured by vibrating flask method quantitative experiment Fabric reaches 98.5% to the antibiotic rate of Escherichia coli, and the antibiotic rate of staphylococcus aureus reaches 99.4%.
Embodiment 4
As shown in Figure 1, a is the infrared spectrum of ramie fabric in figure;B is that the ramie after sodium periodate solution aoxidizes is knitted The infrared spectrum of object;C is the infrared spectrum curve of chitin modified oxidation ramie;Correlation curve a and b can be seen that oxidized Ramie fabric afterwards is in 1730cm- 1Nearby there is the characteristic absorption peak of C=O in aldehyde radical.And it is handled through chitosan finishing liquid Afterwards, C=O stretching vibration peak intensities are all weakened in aldehyde radical in curve c, and in 1660cm-1And 1545cm-1Nearby occur respectively C=N and C-N absorption peaks.This phenomenon illustrates the active aldehyde radical that ramee generates after selective oxidation, can be poly- with shell Amino in sugar subchain combines, and forms imine structure.It can be seen that chitosan is chemically crosslinked with oxidation ramie fabric Reaction, forms firm chemical bonds between the two.

Claims (4)

1. a kind of preparation method with safeguard function linen, which is characterized in that including following preparation process:
1) pretreatment of linen:Linen is added in alkaline solution, after stirring at room temperature, washing, then linen is put Enter in acid solution and impregnate, then wash, alkalization linen is obtained after drying;
2) oxidation processes of linen:By the alkalization linen obtained in prepared periodic acid and step 1) by bath raio 50:1 It is mixed, is protected from light under 40~60 DEG C of water bath conditions, after reaction, linen taken out and washed, first by water Linen after washing, which is placed in glycerin solution, to be impregnated, and is then put it into deionized water and is impregnated again, is washed after drying to obtain the final product Linen is aoxidized, it is spare;
3) preparation of chitosan acetic acid solution:It adds chitosan into acetic acid solution and is dissolved, it is molten to prepare chitosan acetic acid Liquid, wherein the mass concentration of chitosan is 0.5~4% in the chitosan acetic acid solution;
4) preparation of chitin modified oxidation linen:The chitosan acetic acid solution prepared in step 3) is obtained with step 2) Oxidation linen press bath raio 50:1 is mixed, and after infiltration, 1~2h is persistently stirred under water bath condition, then by linen water It washes to be placed in baking oven and be dried, finally washed up to chitin modified oxidation linen after drying, it is spare;
5) composite finishing of the tea polyphenols to chitin modified linen:The chitin modified oxidation hemp that will be prepared in step 4) Object presses bath raio 1:50 put into tea polyphenols solution, and 1~1.5h is persistently stirred under heating, and linen washing is then placed on baking It is dried in case, the rear linen up to composite finishing finally is dried into linen washing;Wherein:
Alkaline solution described in step 1) is the sodium hydroxide solution of 15 ~ 25wt%, the acid solution be mass concentration be 5 ~ 10% acetic acid solution, the time stirred at room temperature are 20 ~ 60min;
A concentration of 2 ~ 10g/L of periodic acid described in step 2), the 0.5 ~ 3h of time being protected from light;Second described in step 3) Acid solution is the acetic acid solution that volumetric concentration is 1 ~ 4%;
The temperature of water-bath is 40 ~ 60 DEG C in step 4), and the linen after washing is placed in baking oven the first preliminary drying 5 under the conditions of 80 DEG C Then ~ 10min bakes 3 min at 140 ~ 160 DEG C, then again dry linen washing;
The temperature of a concentration of 6 ~ 20g/L of tea polyphenols solution described in step 5), the heating are 60 ~ 90 DEG C, after washing Linen is placed in baking oven first 5 ~ 10min of preliminary drying under the conditions of 80 DEG C, then 3 min is baked at 140 ~ 160 DEG C, finally by hemp The rear linen up to composite finishing is dried in object washing.
2. a kind of preparation method with safeguard function linen as described in claim 1, which is characterized in that the linen For any one of ramie, flax or jute.
3. a kind of preparation method with safeguard function linen as described in claim 1, which is characterized in that the chitosan Deacetylation be 80 ~ 95%.
4. one kind have safeguard function linen, which is characterized in that it is described have safeguard function linen be by claim 1 Prepared by a kind of any one of preparation method with safeguard function linen described in ~ 3.
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