CN106351001A - Method for manufacturing ultraviolet-proof textile fabric based on moxa - Google Patents
Method for manufacturing ultraviolet-proof textile fabric based on moxa Download PDFInfo
- Publication number
- CN106351001A CN106351001A CN201610725716.7A CN201610725716A CN106351001A CN 106351001 A CN106351001 A CN 106351001A CN 201610725716 A CN201610725716 A CN 201610725716A CN 106351001 A CN106351001 A CN 106351001A
- Authority
- CN
- China
- Prior art keywords
- artemisiae argyi
- weight portion
- folium artemisiae
- folium
- weight
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 239000004753 textile Substances 0.000 title claims abstract description 13
- 239000000835 fiber Substances 0.000 claims abstract description 30
- 229920000297 Rayon Polymers 0.000 claims abstract description 25
- 241000222336 Ganoderma Species 0.000 claims abstract description 18
- 239000000243 solution Substances 0.000 claims description 24
- 239000008187 granular material Substances 0.000 claims description 13
- 239000000706 filtrate Substances 0.000 claims description 10
- 239000011259 mixed solution Substances 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 5
- 238000005098 hot rolling Methods 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 5
- 238000002137 ultrasound extraction Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 3
- 239000001508 potassium citrate Substances 0.000 claims description 3
- 229960002635 potassium citrate Drugs 0.000 claims description 3
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 claims description 3
- 235000011082 potassium citrates Nutrition 0.000 claims description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- 239000001509 sodium citrate Substances 0.000 claims description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 3
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 claims description 2
- 235000018341 sodium sesquicarbonate Nutrition 0.000 claims description 2
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 claims description 2
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 4
- 230000003266 anti-allergic effect Effects 0.000 abstract description 3
- 230000000843 anti-fungal effect Effects 0.000 abstract description 3
- 230000017531 blood circulation Effects 0.000 abstract description 3
- 230000001737 promoting effect Effects 0.000 abstract description 3
- 238000005406 washing Methods 0.000 abstract description 3
- 230000003110 anti-inflammatory effect Effects 0.000 abstract description 2
- 230000009286 beneficial effect Effects 0.000 abstract description 2
- 235000004347 Perilla Nutrition 0.000 abstract 2
- 241000229722 Perilla <angiosperm> Species 0.000 abstract 2
- 239000004615 ingredient Substances 0.000 abstract 2
- 241000725145 Homalomena Species 0.000 abstract 1
- 230000006750 UV protection Effects 0.000 abstract 1
- 230000002500 effect on skin Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 239000012965 benzophenone Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000002835 absorbance Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- -1 phenyl ester Chemical class 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 235000011181 potassium carbonates Nutrition 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 235000011083 sodium citrates Nutrition 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 1
- 241000040710 Chela Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 231100000215 acute (single dose) toxicity testing Toxicity 0.000 description 1
- 238000011047 acute toxicity test Methods 0.000 description 1
- 230000002052 anaphylactic effect Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- SODJJEXAWOSSON-UHFFFAOYSA-N bis(2-hydroxy-4-methoxyphenyl)methanone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(OC)C=C1O SODJJEXAWOSSON-UHFFFAOYSA-N 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 230000000857 drug effect Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
- D06M16/006—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic with wool-protecting agents; with anti-moth agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
Abstract
The invention provides a method for manufacturing an anti-ultraviolet textile fabric based on moxa, which is characterized by comprising the following steps of: the method comprises the following steps: step S1, selecting ingredients, wherein the ingredients comprise 30-50 parts by weight of moxa, 5-8 parts by weight of viscose fiber, 3-5 parts by weight of obscured homalomena rhizome, 5-8 parts by weight of purple perilla, 2-3 parts by weight of lucid ganoderma and 4-6 parts by weight of perilla leaves; step S2, preparing an extracting solution; step S3, processing the textile; compared with the prior art, the invention has the following beneficial effects: the product prepared by the method makes full use of the antibacterial and antifungal effects of moxa, has antibacterial, anti-inflammatory, antiallergic and blood circulation promoting effects, and has health promotion effect on skin. Moreover, the moxa is tightly combined with the textile, is not easy to volatilize, resists washing, has long efficacy and simultaneously endows the textile with ultraviolet resistance.
Description
Technical field
The present invention is a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi, belongs to textile and manufactures field.
Background technology
In known technology, ultraviolet (ultraviolet rays abbreviation uv) is divided into long wave ultraviolet (uv-
A, 320~400nm), ultraviolet B radiation (uv-b, 280~320nm) and short wave ultraviolet (uv-c, 200~
280nm).Ultraviolet accounts for 6% in daylight, the wherein large percentage of uv-a, and uv-b ratio is less, and ultraviolet is to weaving
Product have harmful effect, and it can not only make textile fade, and also can make the tendering of fibers such as silkworm silk, nylon and cellulose, and strength declines.
Ultraviolet radiation, on fabric, is partly reflected on surface, is partly absorbed by fabric, and remaining then passes through fabric.Ordinary circumstance
Under, transmitance+reflectance+absorbance=100% of ultraviolet, therefore, improves fabric to the absorbance of ultraviolet and anti-
Penetrate the transmitance that rate just can reduce ultraviolet.The ultra-violet absorption that ultraviolet can be absorbed is added on fiber, yarn or fabric
Agent, can reach the purpose of ultraviolet radiation preventing.Because anti-uv finishing fabric is many to make summer clothing, therefore can be straight
Connect and contact human skin.
For this, uvioresistant finishing agent must be carried out with skin anaphylactic test, acute toxicity test and tertogenicity test etc.
Series of security detects, to guarantee product to human security, environmentally friendly.
On textile, the anti-ultraviolet radiation agent of application, except inorganic oxide beyond the region of objective existence, mainly has: (1) metal ion chela at present
Compound, is inorganic compound it is impossible to react with fiber, is only applicable to form the coloured fibre of chelate, mainly carries
The fastness to light of high dyeing;(2) salicylic acid ester type compound, such as phenyl salicylate, salicylic acid -4- tertiary base phenyl ester etc., energy
Absorb the ultraviolet of 280~330nm wavelength, but this kind of compound be relatively low due to fusing point, easily distil, absorptance is relatively low,
And can cause colour-change phenomena under strong illumination, therefore application is less;(3) benzophenone compound, such as 2,4- dihydroxy
Benzophenone, 2,2 '-dihydroxy -4,4 '-dimethoxy-benzophenone, 2- hydroxyl -4- methoxyl group -5- sulfo group
Benzophenone, 2- hydroxyl -4- oxy-octyl benzophenone etc..Because this kind of compound has conjugated structure and hydrogen bond, absorb
Heat energy, fluorescence, phosphorescence can be changed into after ultraviolet, produce hydrogen bond simultaneously and become tautomerism, this structure can accept luminous energy and not
Leading to chain break, and luminous energy can be made to be transformed into heat energy, thus consuming the energy of absorption, being very stable to a certain extent,
There are multiple hydroxyls again, have preferable absorbability to fiber, be the good uvioresistant finishing agent of cotton fiber, but price.
Content of the invention
In view of the shortcomings of the prior art, it is an object of the present invention to provide a kind of anti-ultraviolet yarn fabric system based on Folium Artemisiae Argyi
Make method, to solve the problems, such as to propose in above-mentioned background technology.
To achieve these goals, the present invention is to realize by the following technical solutions: a kind of anti-purple based on Folium Artemisiae Argyi
Outside line yarn fabric manufacture method, comprises the following steps:
Step s1, chooses dispensing, and dispensing includes Folium Artemisiae Argyi 30-50 weight portion, viscose fiber 5-8 weight portion, Rhizoma Homalomenae 3-5 weight
Part, Folium Perillae 5-8 weight portion, Ganoderma 2-3 weight portion, Folium Perillae 4-6 weight portion;
Step s2, makes extracting solution, by Folium Artemisiae Argyi in the environment of ambient temperature is for 26-30 °, naturally dries 60-80min, pick up
Impurity, puts in extruder, extrude 30-50min, by extruding after Folium Artemisiae Argyi granule by weight between ratio add weight be
The water that 2 times of Folium Artemisiae Argyi granule, filters after ultrasonic extraction, forms filtrate, then puts into viscose fiber in extruder, extrudes 30-
50min, the water of viscose fiber 2 times of viscose fiber weight portions of addition after extrusion, in the environment for 26-30 ° for the ambient temperature
Under, stir 20-30min, be subsequently adding Folium Artemisiae Argyi filtrate, form mixed solution, Rhizoma Homalomenae, Folium Perillae, Ganoderma and Folium Perillae are smashed,
Ball grinds, add in mixed solution, in the environment of ambient temperature is for 26-30 °, stir 1-2h, form preliminary extracting solution,
Ph regulator is added, adjustment ph value, between 4-5, forms extracting solution in preliminary extracting solution;
Step s3, processes textile, extracting solution is poured in dye vat, yarn fabric is immersed in dye vat, is 50- in ambient temperature
In the environment of 60 °, stand 30-50min, then yarn fabric is taken out, transport to warehouse for drying, in the ring for 50-70 ° for the ambient temperature
Under border, dry 1-2h, finally by hot-rolling mill by yarn fabric hot-roll forming.
Further, in step s1, described Folium Artemisiae Argyi is a kind of coarse granule Folium Artemisiae Argyi.
Further, in step s2, the Folium Artemisiae Argyi particle diameter after extruding is less than 0.5 millimeter.
Further, described ph regulator be sodium hydroxide, potassium carbonate, sodium carbonate, sodium citrate, potassium citrate, with
And one or more of sodium sesquicarbonate mixture.
Further, in step s2, the fineness after Rhizoma Homalomenae grinds is 85-110 mesh, the fineness after Folium Perillae grinds
For 70-80 mesh, the fineness after Folium Perillae grinds is 80-100 mesh, and the fineness after Ganoderma grinds is 90-120 mesh.
Further, dispensing includes Folium Artemisiae Argyi 30 weight portion, viscose fiber 8 weight portion, Rhizoma Homalomenae 3 weight portion, Folium Perillae 8 weight
Part, Ganoderma 2 weight portion, Folium Perillae 6 weight portion.
Further, dispensing includes Folium Artemisiae Argyi 50 weight portion, viscose fiber 8 weight portion, Rhizoma Homalomenae 5 weight portion, Folium Perillae 8 weight
Part, Ganoderma 3 weight portion, Folium Perillae 6 weight portion.
Beneficial effects of the present invention: a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi of the present invention, using this
The product that method is formed, takes full advantage of the effect of the medicines such as antibacterial, the antifungal of Folium Artemisiae Argyi, and product has anti-inflammation, antiallergic
And blood circulation promoting, there is health-care effect to skin.And, Folium Artemisiae Argyi is tightly combined with yarn fabric, not volatile, anti-washing, medicine
Effect is permanent, gives fabric anti-ultraviolet property simultaneously.
Specific embodiment
Technological means, creation characteristic, reached purpose and effect for making the present invention realize are easy to understand, with reference to
Specific embodiment, is expanded on further the present invention.
The present invention provides a kind of a kind of technical scheme: anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi, including following
Step:
Step s1, chooses dispensing, and dispensing includes Folium Artemisiae Argyi 30-50 weight portion, viscose fiber 5-8 weight portion, Rhizoma Homalomenae 3-5 weight
Part, Folium Perillae 5-8 weight portion, Ganoderma 2-3 weight portion, Folium Perillae 4-6 weight portion;
Step s2, makes extracting solution, by Folium Artemisiae Argyi in the environment of ambient temperature is for 26-30 °, naturally dries 60-80min, pick up
Impurity, puts in extruder, extrude 30-50min, by extruding after Folium Artemisiae Argyi granule by weight between ratio add weight be
The water that 2 times of Folium Artemisiae Argyi granule, filters after ultrasonic extraction, forms filtrate, then puts into viscose fiber in extruder, extrudes 30-
50min, the water of viscose fiber 2 times of viscose fiber weight portions of addition after extrusion, in the environment for 26-30 ° for the ambient temperature
Under, stir 20-30min, be subsequently adding Folium Artemisiae Argyi filtrate, form mixed solution, Rhizoma Homalomenae, Folium Perillae, Ganoderma and Folium Perillae are smashed,
Ball grinds, add in mixed solution, in the environment of ambient temperature is for 26-30 °, stir 1-2h, form preliminary extracting solution,
Ph regulator is added, adjustment ph value, between 4-5, forms extracting solution in preliminary extracting solution;
Step s3, processes textile, extracting solution is poured in dye vat, yarn fabric is immersed in dye vat, is 50- in ambient temperature
In the environment of 60 °, stand 30-50min, then yarn fabric is taken out, transport to warehouse for drying, in the ring for 50-70 ° for the ambient temperature
Under border, dry 1-2h, finally by hot-rolling mill by yarn fabric hot-roll forming.
In step s1, described Folium Artemisiae Argyi is a kind of coarse granule Folium Artemisiae Argyi.
In step s2, the Folium Artemisiae Argyi particle diameter after extruding is less than 0.5 millimeter.
Described ph regulator is sodium hydroxide, potassium carbonate, sodium carbonate, sodium citrate, potassium citrate and bicarbonate
One or more of trisodium mixture.
In step s2, the fineness after Rhizoma Homalomenae grinds is 85-110 mesh, and the fineness after Folium Perillae grinds is 70-80
Mesh, the fineness after Folium Perillae grinds is 80-100 mesh, and the fineness after Ganoderma grinds is 90-120 mesh.
As one embodiment of the present of invention: comprise the following steps:
Step s1, chooses dispensing, and dispensing includes Folium Artemisiae Argyi 30 weight portion, viscose fiber 8 weight portion, Rhizoma Homalomenae 3 weight portion, Folium Perillae 8
Weight portion, Ganoderma 2 weight portion, Folium Perillae 6 weight portion.
Step s2, makes extracting solution, by Folium Artemisiae Argyi in the environment of ambient temperature is for 26-30 °, naturally dries 60-80min,
Pick up impurity, put in extruder, extrude 30-50min, by extruding after Folium Artemisiae Argyi granule by weight between ratio add weight
Measure the water for 2 times of Folium Artemisiae Argyi granule, filter after ultrasonic extraction, form filtrate, then put into viscose fiber in extruder, extruding
30-50min, the water of viscose fiber 2 times of viscose fiber weight portions of addition after extrusion, in the ring for 26-30 ° for the ambient temperature
Under border, stir 20-30min, be subsequently adding Folium Artemisiae Argyi filtrate, form mixed solution, Rhizoma Homalomenae, Folium Perillae, Ganoderma and Folium Perillae are beaten
Broken, ball grinds, add in mixed solution, in the environment of ambient temperature is for 26-30 °, stir 1-2h, form preliminary extraction
Liquid, adds ph regulator in preliminary extracting solution, and adjustment ph value, between 4-5, forms extracting solution;
Step s3, processes textile, extracting solution is poured in dye vat, yarn fabric is immersed in dye vat, is 50- in ambient temperature
In the environment of 60 °, stand 30-50min, then yarn fabric is taken out, transport to warehouse for drying, in the ring for 50-70 ° for the ambient temperature
Under border, dry 1-2h, finally by hot-rolling mill by yarn fabric hot-roll forming.
As one embodiment of the present of invention: comprise the following steps:
Step s1, chooses dispensing, and dispensing includes Folium Artemisiae Argyi 50 weight portion, viscose fiber 8 weight portion, Rhizoma Homalomenae 5 weight portion, Folium Perillae 8
Weight portion, Ganoderma 3 weight portion, Folium Perillae 6 weight portion.
Step s2, makes extracting solution, by Folium Artemisiae Argyi in the environment of ambient temperature is for 26-30 °, naturally dries 60-80min,
Pick up impurity, put in extruder, extrude 30-50min, by extruding after Folium Artemisiae Argyi granule by weight between ratio add weight
Measure the water for 2 times of Folium Artemisiae Argyi granule, filter after ultrasonic extraction, form filtrate, then put into viscose fiber in extruder, extruding
30-50min, the water of viscose fiber 2 times of viscose fiber weight portions of addition after extrusion, in the ring for 26-30 ° for the ambient temperature
Under border, stir 20-30min, be subsequently adding Folium Artemisiae Argyi filtrate, form mixed solution, Rhizoma Homalomenae, Folium Perillae, Ganoderma and Folium Perillae are beaten
Broken, ball grinds, add in mixed solution, in the environment of ambient temperature is for 26-30 °, stir 1-2h, form preliminary extraction
Liquid, adds ph regulator in preliminary extracting solution, and adjustment ph value, between 4-5, forms extracting solution;
Step s3, processes textile, extracting solution is poured in dye vat, yarn fabric is immersed in dye vat, is 50- in ambient temperature
In the environment of 60 °, stand 30-50min, then yarn fabric is taken out, transport to warehouse for drying, in the ring for 50-70 ° for the ambient temperature
Under border, dry 1-2h, finally by hot-rolling mill by yarn fabric hot-roll forming.
The product being formed using this method, takes full advantage of the effect of the medicines such as antibacterial, the antifungal of Folium Artemisiae Argyi, product has anti-
Bacterium antiinflammatory, antiallergic and blood circulation promoting, have health-care effect to skin.And, Folium Artemisiae Argyi is tightly combined with yarn fabric, is difficult to wave
Send out, anti-washing, drug effect is permanent, give fabric anti-ultraviolet property simultaneously.
Ultimate principle and principal character and the advantages of the present invention of the present invention have been shown and described above, for this area skill
It is clear that the invention is not restricted to the details of above-mentioned one exemplary embodiment for art personnel, and in the spirit without departing substantially from the present invention or
In the case of basic feature, the present invention can be realized in other specific forms.Therefore, no matter from the point of view of which point, all should be by
Embodiment regards exemplary as, and is nonrestrictive, the scope of the present invention by claims rather than on state
Bright restriction, it is intended that all changes in the implication and scope of the equivalency of claim that fall are included in the present invention
Interior.
Moreover, it will be appreciated that although this specification is been described by according to embodiment, not each embodiment only wraps
Containing an independent technical scheme, only for clarity, those skilled in the art should for this narrating mode of description
Using description as an entirety, the technical scheme in each embodiment can also form those skilled in the art through appropriately combined
Understandable other embodiment.
Claims (7)
1. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi it is characterised in that: comprise the following steps:
Step s1, chooses dispensing, and dispensing includes Folium Artemisiae Argyi 30-50 weight portion, viscose fiber 5-8 weight portion, Rhizoma Homalomenae 3-5 weight
Part, Folium Perillae 5-8 weight portion, Ganoderma 2-3 weight portion, Folium Perillae 4-6 weight portion;
Step s2, makes extracting solution, by Folium Artemisiae Argyi in the environment of ambient temperature is for 26-30 °, naturally dries 60-80min, pick up
Impurity, puts in extruder, extrude 30-50min, by extruding after Folium Artemisiae Argyi granule by weight between ratio add weight be
The water that 2 times of Folium Artemisiae Argyi granule, filters after ultrasonic extraction, forms filtrate, then puts into viscose fiber in extruder, extrudes 30-
50min, the water of viscose fiber 2 times of viscose fiber weight portions of addition after extrusion, in the environment for 26-30 ° for the ambient temperature
Under, stir 20-30min, be subsequently adding Folium Artemisiae Argyi filtrate, form mixed solution, Rhizoma Homalomenae, Folium Perillae, Ganoderma and Folium Perillae are smashed,
Ball grinds, add in mixed solution, in the environment of ambient temperature is for 26-30 °, stir 1-2h, form preliminary extracting solution,
Ph regulator is added, adjustment ph value, between 4-5, forms extracting solution in preliminary extracting solution;
Step s3, processes textile, extracting solution is poured in dye vat, yarn fabric is immersed in dye vat, is 50- in ambient temperature
In the environment of 60 °, stand 30-50min, then yarn fabric is taken out, transport to warehouse for drying, in the ring for 50-70 ° for the ambient temperature
Under border, dry 1-2h, finally by hot-rolling mill by yarn fabric hot-roll forming.
2. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi according to claim 1 it is characterised in that: in step
In rapid s1, described Folium Artemisiae Argyi is a kind of coarse granule Folium Artemisiae Argyi.
3. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi according to claim 1 it is characterised in that: in step
In rapid s2, the Folium Artemisiae Argyi particle diameter after extruding is less than 0.5 millimeter.
4. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi according to claim 1 it is characterised in that: described
Ph regulator is one of sodium hydroxide, potassium carbonate, sodium carbonate, sodium citrate, potassium citrate and sodium sesquicarbonate
Or multiple mixture.
5. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi according to claim 1 it is characterised in that: in step
In rapid s2, the fineness after Rhizoma Homalomenae grinds is 85-110 mesh, and the fineness after Folium Perillae grinds is 70-80 mesh, Folium Perillae grinds
Fineness afterwards is 80-100 mesh, and the fineness after Ganoderma grinds is 90-120 mesh.
6. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi according to claim 1 it is characterised in that: dispensing
Including Folium Artemisiae Argyi 30 weight portion, viscose fiber 8 weight portion, Rhizoma Homalomenae 3 weight portion, Folium Perillae 8 weight portion, Ganoderma 2 weight portion, Folium Perillae 6
Weight portion.
7. a kind of anti-ultraviolet yarn fabric manufacture method based on Folium Artemisiae Argyi according to claim 1 it is characterised in that: dispensing
Including Folium Artemisiae Argyi 50 weight portion, viscose fiber 8 weight portion, Rhizoma Homalomenae 5 weight portion, Folium Perillae 8 weight portion, Ganoderma 3 weight portion, Folium Perillae 6
Weight portion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610725716.7A CN106351001A (en) | 2016-08-26 | 2016-08-26 | Method for manufacturing ultraviolet-proof textile fabric based on moxa |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610725716.7A CN106351001A (en) | 2016-08-26 | 2016-08-26 | Method for manufacturing ultraviolet-proof textile fabric based on moxa |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106351001A true CN106351001A (en) | 2017-01-25 |
Family
ID=57854906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610725716.7A Pending CN106351001A (en) | 2016-08-26 | 2016-08-26 | Method for manufacturing ultraviolet-proof textile fabric based on moxa |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106351001A (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101736605A (en) * | 2009-12-24 | 2010-06-16 | 江南大学 | Single bath finishing technology for antibacterium and dyeing of textile by natural products |
CN102162187A (en) * | 2011-04-13 | 2011-08-24 | 姜开明 | Ultraviolet ray resistant textile containing moxa water extracts and production method thereof |
CN102357161A (en) * | 2011-10-26 | 2012-02-22 | 宋溪岩 | Moxa composition, and preparation method and application thereof |
CN102677458A (en) * | 2012-05-05 | 2012-09-19 | 南通市鸿基织造有限公司 | Healthcare fabric manufacturing process |
CN103835138A (en) * | 2014-01-28 | 2014-06-04 | 张铁末 | Traditional Chinese medicine gray cloth used for healthcare shoes and preparation method thereof |
CN103835126A (en) * | 2013-12-12 | 2014-06-04 | 青岛无为保温材料有限公司 | Novel mildew preventive for textile, and preparation method thereof |
-
2016
- 2016-08-26 CN CN201610725716.7A patent/CN106351001A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101736605A (en) * | 2009-12-24 | 2010-06-16 | 江南大学 | Single bath finishing technology for antibacterium and dyeing of textile by natural products |
CN102162187A (en) * | 2011-04-13 | 2011-08-24 | 姜开明 | Ultraviolet ray resistant textile containing moxa water extracts and production method thereof |
CN102357161A (en) * | 2011-10-26 | 2012-02-22 | 宋溪岩 | Moxa composition, and preparation method and application thereof |
CN102677458A (en) * | 2012-05-05 | 2012-09-19 | 南通市鸿基织造有限公司 | Healthcare fabric manufacturing process |
CN103835126A (en) * | 2013-12-12 | 2014-06-04 | 青岛无为保温材料有限公司 | Novel mildew preventive for textile, and preparation method thereof |
CN103835138A (en) * | 2014-01-28 | 2014-06-04 | 张铁末 | Traditional Chinese medicine gray cloth used for healthcare shoes and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101525777B (en) | Viscose fiber with mint antibacterial function and preparation method thereof | |
CN100462486C (en) | Viscose fibre with tea anti-bacterial anti-foul function and its preparing method | |
CN105603557B (en) | Traditional Chinese medicine health-care regenerated cellulose fiber and preparation method thereof | |
CN102220648B (en) | Preparation method of traditional Chinese medicine velvet viscose fiber | |
US8361167B2 (en) | Natural hair dyes | |
CN102644125B (en) | Method for preparing polychromatic viscose fibers | |
CN104514040B (en) | A kind of preparation method of plant source coloured antibiotic viscose fiber | |
CN101195714A (en) | Method for producing giant knotweed rhizome natural dye and uses thereof | |
CN101857977A (en) | Tea fiber capable of releasing anion and preparation method thereof | |
CN101165232A (en) | Luminescent core-skin composite fiber and preparation method thereof | |
CN107385597B (en) | Copper ion antibacterial nylon yarn for mesh fabric production | |
CN102174719A (en) | Microporous photocatalyst bamboo charcoal polyester modified short fiber and preparation method thereof | |
CN102477601A (en) | Skin whitening sunscreen yarn | |
CN102704143B (en) | Nanometer ZrO2 compound function fabric and manufacturing method and applications | |
CN104047099A (en) | Manufacturing technology of health-care type blended knitted fabric | |
CN104389100A (en) | Fluorescent sunscreen fabric production method | |
Baseri | Ecological dyeing of cotton fabric with Matricaria recutita L. in the presence of human hair keratins as an alternative copartner to metallic mordants | |
CN102162187A (en) | Ultraviolet ray resistant textile containing moxa water extracts and production method thereof | |
CN108978282A (en) | A kind of preparation method of Uvr Protective Fabric | |
CN109505028B (en) | Long-acting broad-spectrum antibacterial Tiancha fiber and preparation method thereof | |
CN108691063B (en) | Blended and interwoven fabric of mint fibers, soybean fibers and polyester fibers and manufacturing method thereof | |
CN110438578A (en) | A kind of color-changing face fabric and its production method | |
CN106351001A (en) | Method for manufacturing ultraviolet-proof textile fabric based on moxa | |
CN102704142B (en) | Zirconium nano composite functional tencel fabric and weaving, dyeing and finishing process and application thereof | |
CN102677227B (en) | Composite tea carbon polyster fiber of continuous high-strength core sheath |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170125 |
|
RJ01 | Rejection of invention patent application after publication |