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CN108221081A - High intensity carboxymethyl cellulose/sodium alginate blended fiber and preparation method thereof - Google Patents

High intensity carboxymethyl cellulose/sodium alginate blended fiber and preparation method thereof Download PDF

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Publication number
CN108221081A
CN108221081A CN201711329415.3A CN201711329415A CN108221081A CN 108221081 A CN108221081 A CN 108221081A CN 201711329415 A CN201711329415 A CN 201711329415A CN 108221081 A CN108221081 A CN 108221081A
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sodium alginate
carboxymethyl cellulose
blended fiber
high intensity
preparation
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CN108221081B (en
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郝继海
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New Qingdao Mstar Technology Ltd
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New Qingdao Mstar Technology Ltd
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/02Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from cellulose, cellulose derivatives, or proteins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/28Polysaccharides or their derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/06Wet spinning methods
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/12Stretch-spinning methods
    • D01D5/14Stretch-spinning methods with flowing liquid or gaseous stretching media, e.g. solution-blowing
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/28Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
    • D01D5/30Conjugate filaments; Spinnerette packs therefor
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • D01F1/103Agents inhibiting growth of microorganisms
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/18Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from other substances
    • 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
    • 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
    • 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
    • D06M2101/08Esters or ethers of cellulose

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  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Textile Engineering (AREA)
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  • Artificial Filaments (AREA)
  • Materials For Medical Uses (AREA)

Abstract

The present invention relates to a kind of high intensity carboxymethyl cellulose/sodium alginate blended fibers, further relate to a kind of preparation method of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber.The preparation method of the high intensity carboxymethyl cellulose/sodium alginate blended fiber includes the following steps:(1) preparation of co-blended spinning solution;(2) it adds in lauryl sodium sulfate and mixes;(3) deaeration is filtered, is solidified by three coagulating baths;(4) the 4th drawing-off is carried out after water washing bath washing;(5) blended fiber after the washing obtained by step (4) is impregnated 10 15 minutes with mass concentration for 20% 30% glucose solution;(6) dry, winding.The present invention improves alginate fibre intensity and spinnability by improving preparation process, expands the application range of carboxymethyl cellulose/sodium alginate blended fiber.

Description

High intensity carboxymethyl cellulose/sodium alginate blended fiber and preparation method thereof
Technical field
The present invention relates to fibre manufacturing technology fields, and in particular to a kind of high intensity carboxymethyl cellulose/sodium alginate is common Combined filament further relates to a kind of preparation method of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber.
Background technology
Carboxymethyl cellulose and sodium alginate are polysaccharide compounds cheap and easy to get, have renewable, source is wide etc. Advantage.Alginic acid (Alginic acid) be with extracted in natural seaweed formed by monosaccharide aldehydic acid linear polymerization it is more Sugar, seaweed acid monomers are β-Isosorbide-5-Nitrae-D-MANNOSE aldehydic acid (M) and α-Isosorbide-5-Nitrae-L- guluronic acids (G), and alginic acid leads in the application It is often utilized in the form of alginate, such as sodium alginate, calcium alginate.Due to the good biological degradability of alginic acid fibre and Biocompatibility and high-hygroscopicity and gelation have been widely used in the fields such as chemistry, biology, medicine, food, and It is prepared by the membrane material for being widely used in multiple use with its good film forming.Carboxymethyl cellulose is also known as " carboxymethyl fibre The plain sodium of dimension ", " sanlose ", " CMC ", are after the hydrogen atom of light base on cellulose glucose ring is replaced by carboxymethyl A kind of water-soluble cellulose ether, carboxymethyl cellulose is that use scope is most wide in the world today, cellulose kind of dosage maximum Class.Sodium carboxymethylcellulose has nontoxic, good biocompatibility, degradability, recyclability and hygroscopic characteristic.
However, sodium alginate film quality is crisp, fibre strength is not high, spinnability is poor, and water resistance is very poor, is limited on System.Relatively low with the most of intensity of fiber that sodium carboxymethylcellulose raw material obtains, obtained product aft-loaded airfoil performance is very undesirable. The blended fiber of obtained shuttle sodium carboxymethylcellulose pyce domestic at present and sodium alginate, technique is generally by wet spinning technology Spinning solution from spinning head is squeezed out, into calcium chloride coagulation bath, then blending fibre is obtained after drawing-off, washing, drying, winding Dimension.It is primarily present following deficiency:Large viscosity between fiber, spinnability is poor, and fibre strength is not high.
Invention content
An object of the present invention is the above-mentioned deficiency for the prior art, provide a kind of high intensity carboxymethyl cellulose/ The preparation method of sodium alginate blended fiber improves alginate fibre intensity and spinnability by improving preparation process.
In order to solve the above-mentioned technical problem, the present invention is using following technical scheme, a kind of high intensity carboxymethyl cellulose/sea The preparation method of mosanom blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:The weight ratio of 2-10 is dissolved in In deionized water, stir 2-3 hours, obtain spinning solution;
(2) spinning solution is put to 0-4 DEG C and stands preservation 6-10 hours, taken out, is put into water-bath concussion pot, 40-50 DEG C, Concussion processing 20-30 minutes, then add in lauryl sodium sulfate under conditions of 200-300r/min, continue to be placed on water-bath concussion 40-50 DEG C in pot, processing 50-60 minutes is shaken under conditions of 200-300r/min, the additive amount of lauryl sodium sulfate is sea The 1% of mosanom quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixer ultrasonic mixing 20-30 minutes, will mixed Good spinning solution, which is poured into dissolution kettle, is filtered deaeration, is then squeezed out after metering pump from spinneret to first of coagulating bath In, through first time drawing-off, first of coagulating bath is the calcium chloride water that mass fraction is 1-2%, and first of coagulating bath is coagulated Solid temperature degree is 50-55 DEG C, and setting time is 2-3 minutes;It is water-soluble with the sodium hydroxide that mass fraction is 10% after first time drawing-off Liquid washs, and is re-introduced into second coagulating bath, and through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water With 3-4:1:2 ratio is prepared, and the setting temperature of second coagulating bath is 20-30 DEG C, and setting time is 1-3 minutes;The It is washed with deionized and then is introduced into the coagulating bath of third road after secondary drawing-off, third time drawing-off, third road coagulating bath is matter Amount score is 8-10% calcium chloride waters, and the temperature of third road coagulating bath is 25-30 DEG C, and setting time is 3-4 minutes;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing;
(5) glucose solution for being 20%-30% with mass concentration by the blended fiber after the washing obtained by step (4) It impregnates 10-15 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through drying, rolling step up to the present invention high intensity carboxylic Methylcellulose/sodium alginate blended fiber.
Pass through high intensity carboxymethyl cellulose/sodium alginate blended fiber hygroscopicity obtained by the preparation method of the present invention More preferably, it is 22-25g/g fibers, therefore can preferably absorb wound penetrating fluid to the liquid absorption amount of distilled water.The blending of the present invention The postoperative use of fiber can mitigate oedema and surface of a wound stimulation, the increase of bacterium wrapping property, and wound degree of being adhered smaller, wound more holds Easily healing is not easy to be adhered wound when removing and causes secondary damage to wound.In addition, the high intensity carboxymethyl obtained by the present invention Cellulose/sodium alginate blended fiber fracture strength is high, and dimension fracture strength is 2.6~3.1cN/dtex.In addition, pass through the present invention Preparation process reduce viscosity between fiber, it is poor to solve carboxymethyl cellulose of the prior art/sodium alginate spinnability The problem of.Wherein, the viscosity of spinning solution can be advantageously reduced by the processing of step (2), increases its spinnability, and can improve Dispersibility increases carboxymethyl cellulose and the mutual compatibility of sodium alginate.In step (4), fibre can be washed away by water washing bath Ion in the presence of the coagulating bath of dimension table face.Further blended fiber can be modified by the processing of step (5), can be reduced Viscosity between fiber solves the problems, such as that carboxymethyl cellulose of the prior art/sodium alginate spinnability is poor.As it can be seen that this hair Bright not only hygroscopicity significantly increases, but also obtained blended fiber intensity is high, and viscosity is low between fiber, and spinnability is high.
Further, in step (1), in carboxymethyl cellulose/sodium alginate co-blended spinning solution, the quality of sodium alginate Score is 6%-15%, preferably 8%-10%.
Further, the molecular weight of the sodium alginate is 300000-400000, and M/G values are 2-2.5.
Further, the drafting multiple of the first time drawing-off of the fiber is 1-2 times, and the drafting multiple of second of drawing-off is 1-1.5 times, the drafting multiple of third time drawing-off is 2-3 times, and the drafting multiple of the 4th drawing-off is 1-1.5 times.
Preferably, plants essential oil is further included in the spinning mixed solution of step (1), the dosage of plants essential oil is sodium alginate The 0.5-1.0% of quality, the plants essential oil can be Rosa Damascana.
Preferably, antiseptic is further included in the spinning mixed solution of step (1), the dosage of antiseptic is sodium alginate quality 0.5-1.0%, the antiseptic can be Flos Lonicerae extractive solution or root bark of tree peony decoction liquor.
Further, the drying means of step (6) is 60 DEG C of drying.
Further, the drying means of step (6) is vacuum freeze drying.Its advantage is conducive to improve alginate fibre Mechanical performance and three-dimensional porous structure.
The invention also discloses a kind of high intensity carboxymethyl cellulose/sodium alginates by obtained by above-mentioned preparation method Blended fiber.
The invention also discloses a kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fibers to make medical defend The application of raw dressing.
Compared with prior art, the beneficial effects of the invention are as follows:
(1) present invention is improved and right by the proportioning to carboxymethyl cellulose and sodium alginate and mixed method The preparation processes such as the setting time of the ingredient of coagulating bath, temperature and fiber are improved, not only increase alginate fibre intensity and Spinnability reduces viscosity between fiber, reduces the difficulty of processing of blended fiber, also improve blended fiber hygroscopicity, expands The application range of carboxymethyl cellulose/sodium alginate blended fiber.
(2) high intensity carboxymethyl cellulose/sodium alginate blended fiber hygroscopicity obtained by preparation method of the invention More preferably, therefore wound penetrating fluid can preferably be absorbed.The postoperative use of blended fiber of the present invention can mitigate oedema and the surface of a wound Stimulation, the increase of bacterium wrapping property, wound degree of being adhered smaller, wound are easier to heal, are not easy to be adhered wound pair when removing Wound causes secondary damage.
Specific embodiment
Following embodiment facilitates a better understanding of the present invention, but does not limit the present invention.Experiment in following embodiments Method is conventional method unless otherwise specified.
Embodiment 1
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:2 weight ratio dissolve in from It in sub- water, stirs 3 hours, obtains spinning solution, in spinning solution, the mass fraction of sodium alginate is 12%;
(2) spinning solution is put to 0 DEG C and stands preservation 8 hours, taken out, is put into water-bath concussion pot, 40 DEG C, 300r/min Under conditions of concussion processing 30 minutes, then add in lauryl sodium sulfate, continue water-bath shake pot in 40 DEG C, 300r/min Under conditions of concussion processing 50 minutes, the additive amount of lauryl sodium sulfate is the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 25 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 2%, and the setting temperature of first of coagulating bath is 50 DEG C, setting time is 2 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 3:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 25 DEG C, and setting time is 2 minutes;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is that 8% calcium chloride is water-soluble Liquid, the temperature of third road coagulating bath is 28 DEG C, and setting time is 4 minutes;
The drafting multiple of the first time drawing-off of the fiber is 1 times, and the drafting multiple of second of drawing-off is 1.5 times, third The drafting multiple of secondary drawing-off is 2 times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1.5 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 24% is impregnated 15 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through vacuum freeze drying, rolling step up to the present invention High intensity carboxymethyl cellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Embodiment 2
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:4 weight ratio dissolve in from It in sub- water, stirs 2 hours, obtains spinning solution, in spinning solution, the mass fraction of sodium alginate is 10%;
(2) spinning solution is put to 0 DEG C and stands preservation 6 hours, taken out, is put into water-bath concussion pot, 45 DEG C, 200r/min Under conditions of concussion processing 20 minutes, then add in lauryl sodium sulfate, continue water-bath shake pot in 45 DEG C, 200r/min Under conditions of concussion processing 60 minutes, the additive amount of lauryl sodium sulfate is the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 20 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 1%, and the setting temperature of first of coagulating bath is 55 DEG C, setting time is 3 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 4:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 20 DEG C, and setting time is 2 minutes;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is that 9% calcium chloride is water-soluble Liquid, the temperature of third road coagulating bath is 25 DEG C, and setting time is 4 minutes;
The drafting multiple of the first time drawing-off of the fiber is 1.5 times, and the drafting multiple of second of drawing-off is 1 times, third The drafting multiple of secondary drawing-off is 3 times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1.2 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 30% is impregnated 12 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through vacuum freeze drying, rolling step up to the present invention High intensity carboxymethyl cellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Embodiment 3
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:5 weight ratio dissolve in from It in sub- water, stirs 3 hours, obtains in spinning solution spinning solution, the mass fraction of sodium alginate is 10%;
(2) spinning solution is put to 2 DEG C and stands preservation 8 hours, taken out, is put into water-bath concussion pot, 48 DEG C, 300r/min Under conditions of concussion processing 20 minutes, then add in lauryl sodium sulfate, continue water-bath shake pot in 45 DEG C, 300r/min Under conditions of concussion processing 60 minutes, the additive amount of lauryl sodium sulfate is the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 25 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 2%, and the setting temperature of first of coagulating bath is 55 DEG C, setting time is 2 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 3:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 30 DEG C, and setting time is 2 minutes;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is that 9% calcium chloride is water-soluble Liquid, the temperature of third road coagulating bath is 28 DEG C, and setting time is 3 minutes;
The drafting multiple of the first time drawing-off of the fiber is 2 times, and the drafting multiple of second of drawing-off is 1 times, third time The drafting multiple of drawing-off is 2.5 times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 30% is impregnated 12 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through vacuum freeze drying, rolling step up to the present invention High intensity carboxymethyl cellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Embodiment 4
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:5 weight ratio dissolve in from In sub- water, stir 2 hours, obtain spinning solution, in spinning solution, the mass fraction 8% of sodium alginate;
(2) spinning solution is put to 4 DEG C and stands preservation 10 hours, taken out, is put into water-bath concussion pot, 45 DEG C, 250r/ Concussion processing 30 minutes, then add in lauryl sodium sulfate under conditions of min, continue 45 DEG C, 250r/ in pot is shaken in water-bath Concussion processing 50 minutes under conditions of min, the additive amount of lauryl sodium sulfate are the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 30 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 1%, and the setting temperature of first of coagulating bath is 50 DEG C, setting time is 3 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 3:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 28 DEG C, and setting time is 2 minutes;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is 10% calcium chloride water Solution, the temperature of third road coagulating bath is 30 DEG C, and setting time is 3 minutes;
The drafting multiple of the first time drawing-off of the fiber is 1.5 times, and the drafting multiple of second of drawing-off is 1.2 times, the The drafting multiple of drawing-off is 2 times three times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1.2 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 30% is impregnated 10 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through vacuum freeze drying, rolling step up to the present invention High intensity carboxymethyl cellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Embodiment 5
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:6 weight ratio dissolve in from It in sub- water, stirs 3 hours, obtains spinning solution, in spinning solution, the mass fraction of sodium alginate is 9%;
(2) spinning solution is put to 4 DEG C and stands preservation 6 hours, taken out, is put into water-bath concussion pot, 48 DEG C, 200r/min Under conditions of concussion processing 30 minutes, then add in lauryl sodium sulfate, continue water-bath shake pot in 50 DEG C, 300r/min Under conditions of concussion processing 50 minutes, the additive amount of lauryl sodium sulfate is the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 25 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 2%, and the setting temperature of first of coagulating bath is 55 DEG C, setting time is 3 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 3:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 20 DEG C, and setting time is 1 minute;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is that 8% calcium chloride is water-soluble Liquid, the temperature of third road coagulating bath is 30 DEG C, and setting time is 4 minutes;
The drafting multiple of the first time drawing-off of the fiber is 1.5 times, and the drafting multiple of second of drawing-off is 1.5 times, the The drafting multiple of drawing-off is 2.5 times three times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1.5 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 25% is impregnated 15 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through vacuum freeze drying, rolling step up to the present invention High intensity carboxymethyl cellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Embodiment 6
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:8 weight ratio dissolve in from It in sub- water, stirs 2 hours, obtains spinning solution, in spinning solution, the mass fraction of sodium alginate is 6%;
(2) spinning solution is put to 3 DEG C and stands preservation 7 hours, taken out, is put into water-bath concussion pot, 50 DEG C, 200r/min Under conditions of concussion processing 25 minutes, then add in lauryl sodium sulfate, continue water-bath shake pot in 45 DEG C, 240r/min Under conditions of concussion processing 50 minutes, the additive amount of lauryl sodium sulfate is the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 20 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 2%, and the setting temperature of first of coagulating bath is 50 DEG C, setting time is 2 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 4:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 30 DEG C, and setting time is 3 minutes;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is 10% calcium chloride water Solution, the temperature of third road coagulating bath is 30 DEG C, and setting time is 3 minutes;
The drafting multiple of the first time drawing-off of the fiber is 2 times, and the drafting multiple of second of drawing-off is 1 times, third time The drafting multiple of drawing-off is 2 times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1.2 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 20% is impregnated 15 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through vacuum freeze drying, rolling step up to the present invention High intensity carboxymethyl cellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Embodiment 7
A kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, includes the following steps:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:10 weight ratio is dissolved in It in ionized water, stirs 3 hours, obtains spinning solution, in spinning solution, the mass fraction of sodium alginate is 15%;
(2) spinning solution is put to 2 DEG C and stands preservation 8 hours, taken out, is put into water-bath concussion pot, 40 DEG C, 300r/min Under conditions of concussion processing 20 minutes, then add in lauryl sodium sulfate, continue water-bath shake pot in 50 DEG C, 200r/min Under conditions of concussion processing 60 minutes, the additive amount of lauryl sodium sulfate is the 1% of sodium alginate quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixing 30 minutes in ultrasonic mixer, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 1%, and the setting temperature of first of coagulating bath is 55 DEG C, setting time is 2 minutes;It is washed, is re-introduced into the sodium hydrate aqueous solution that mass fraction is 10% after first time drawing-off Into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 4:1:2 ratio It is prepared, the setting temperature of second coagulating bath is 25 DEG C, and setting time is 1 minute;Deionized water is used after second of drawing-off It washs and then is introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is that 8% calcium chloride is water-soluble Liquid, the temperature of third road coagulating bath is 30 DEG C, and setting time is 4 minutes;
The drafting multiple of the first time drawing-off of the fiber is 1 times, and the drafting multiple of second of drawing-off is 1.2 times, third The drafting multiple of secondary drawing-off is 3 times;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing, the 4th drawing-off Drafting multiple is 1 times;
(5) glucose solution that the blended fiber mass concentration after the washing obtained by step (4) is 30% is impregnated 10 minutes;
(6) by after the immersion obtained by step (5) blended fiber drying, rolling step up to the present invention high intensity carboxylic Methylcellulose/sodium alginate blended fiber.
A kind of high intensity carboxymethyl cellulose/sodium alginate blended fiber by obtained by above-mentioned preparation method.
A kind of above-mentioned high intensity carboxymethyl cellulose/sodium alginate blended fiber is in the application for making medical sanitary dressing.
Performance measurement is carried out to the high intensity carboxymethyl cellulose obtained by embodiment 1-7/sodium alginate blended fiber.
The measure of liquid absorption amount:0.1g blended fiber samples are weighed, is placed in the distilled water of 50mL and impregnates 30min;It will inhale Fiber centrifugal dehydration 15min after water, centrifuge speed 2000r/min weigh, and quality is denoted as M1;Then fiber is placed in It dries to constant weight, weighs, quality is denoted as M2 in 105 DEG C of baking ovens.Liquid absorption amount N=(M1-M2)/M2 of fiber.The results show that embodiment High intensity carboxymethyl cellulose/sodium alginate blended fiber obtained by 1-7 is 22-25g/g fibers to the liquid absorption amount of distilled water. As it can be seen that the liquid absorption amount of the present invention significantly improves, wound penetrating fluid can be preferably absorbed.
Fracture strength measures:Reference《GB/T 14337-2008 man-made staple fibres Wellas stretch method for testing performance》To reality It applies high intensity carboxymethyl cellulose/sodium alginate blended fiber obtained by a 1-7 and carries out fracture strength measure, the results show that The fracture strength of high intensity carboxymethyl cellulose/sodium alginate blended fiber obtained by embodiment 1-7 is 2.6~3.1cN/ dtex。
The above is only the preferred embodiment of the present invention, it should be pointed out that:For the ordinary skill people of the art For member, without departing from the principle of the present invention, several improvement can also be made, these improvement should be regarded as the guarantor of the present invention Protect range.

Claims (10)

1. a kind of preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber, it is characterised in that:Including following step Suddenly:
(1) preparation of co-blended spinning solution:By carboxymethyl cellulose and sodium alginate according to 1:The weight ratio of 2-10 dissolve in from In sub- water, stir 2-3 hours, obtain spinning solution;
(2) spinning solution is put to 0-4 DEG C and stands preservation 6-10 hours, taken out, is put into water-bath concussion pot, 40-50 DEG C, 200- Concussion processing 20-30 minutes, then add in lauryl sodium sulfate under conditions of 300r/min, continue to be placed in water-bath concussion pot 40-50 DEG C, concussion processing 50-60 minute under conditions of 200-300r/min, the additive amount of lauryl sodium sulfate is alginic acid The 1% of sodium quality;
(3) mixed solution obtained by step (2) is put into ultrasonic mixer ultrasonic mixing 20-30 minutes, by what is mixed Spinning solution pours into and deaeration is filtered in dissolution kettle, is then squeezed out after metering pump from spinneret into first of coagulating bath, warp First time drawing-off, first of coagulating bath are the calcium chloride water that mass fraction is 1-2%, the setting temperature of first of coagulating bath It it is 50-55 DEG C, setting time is 2-3 minutes;It is washed after first time drawing-off with the sodium hydrate aqueous solution that mass fraction is 10%, It is re-introduced into second coagulating bath, through second of drawing-off, second coagulating bath is ethyl alcohol, methanol and deionized water with 3-4:1: 2 ratio is prepared, and the setting temperature of second coagulating bath is 20-30 DEG C, and setting time is 1-3 minutes;Second of drawing-off After be washed with deionized and then be introduced into the coagulating bath of third road, third time drawing-off, third road coagulating bath is that mass fraction is 8-10% calcium chloride waters, the temperature of third road coagulating bath is 25-30 DEG C, and setting time is 3-4 minutes;
(4) fiber after three coagulating baths is subjected to the 4th drawing-off after water washing bath washing;
(5) blended fiber after the washing obtained by step (4) is impregnated with the glucose solution that mass concentration is 20%-30% 10-15 minutes;
(6) by the blended fiber after the immersion obtained by step (5) through drying, rolling step up to the present invention high intensity carboxymethyl Cellulose/sodium alginate blended fiber.
2. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:In step (1), in carboxymethyl cellulose/sodium alginate co-blended spinning solution, the mass fraction of sodium alginate is 6%- 15%.
3. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:In step (1), in carboxymethyl cellulose/sodium alginate co-blended spinning solution, the mass fraction of sodium alginate is 8%- 10%.
4. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:The molecular weight of the sodium alginate is 300000-400000, and M/G values are 2-2.5.
5. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:The drafting multiple of the first time drawing-off of the fiber is 1-2 times, and the drafting multiple of second of drawing-off is 1-1.5 times, third The drafting multiple of secondary drawing-off is 2-3 times, and the drafting multiple of the 4th drawing-off is 1-1.5 times.
6. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:Plants essential oil is further included in the spinning mixed solution of step (1), the dosage of plants essential oil is the 0.5- of sodium alginate quality 1.0%.
7. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:Antiseptic is further included in the spinning mixed solution of step (1), the dosage of antiseptic is the 0.5- of sodium alginate quality 1.0%.
8. the preparation method of high intensity carboxymethyl cellulose/sodium alginate blended fiber according to claim 1, feature It is:The drying means of step (6) is vacuum freeze drying.
9. the preparation of high intensity carboxymethyl cellulose/sodium alginate blended fiber described in a kind of any one of claim 1-8 Blended fiber obtained by method.
10. the blended fiber described in a kind of claim 9 is in the application for making medical sanitary dressing.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108914389A (en) * 2018-07-11 2018-11-30 高昕文 A kind of preparation method of composite fiber spunlace mask base cloth
CN109137502A (en) * 2018-08-07 2019-01-04 苏州市天翱特种织绣有限公司 A kind of preparation method of moisture absorbing and sweat releasing knitting fabric
CN109627498A (en) * 2018-11-27 2019-04-16 青岛大学 A kind of sodium alginate-cellulose derivative blended membrane/fiber and preparation method thereof
CN109868525A (en) * 2019-02-19 2019-06-11 青岛海赛尔新材料科技有限公司 A kind of preparation method of high intensity seaweed and polyvinyl alcohol blending fiber
CN109972233A (en) * 2019-02-19 2019-07-05 青岛大学 Preparation method of biodegradable alginate fiber with high strength and high toughness
CN110241481A (en) * 2019-05-28 2019-09-17 福建美可纸业有限公司 A kind of superabsorbent water composite fibre and preparation method thereof
CN112127009A (en) * 2020-09-11 2020-12-25 嘉兴学院 Cellulose/calcium alginate blend fiber with skin-core structure and preparation method thereof
CN116730691A (en) * 2023-05-25 2023-09-12 东莞市欧丽亚环保材料有限公司 Ceramic tile adhesive and preparation method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103060946A (en) * 2012-12-21 2013-04-24 稳健实业(深圳)有限公司 Blend fibers of alginate and sodium carboxymethyl cellulose and preparation method and application thereof
CN105544002A (en) * 2015-12-18 2016-05-04 厦门百美特生物材料科技有限公司 Superabsorbent composite fiber and preparation method thereof
CN106702533A (en) * 2015-07-27 2017-05-24 吴玉松 High-strength alginate composite fiber, and preparation method and use thereof
WO2017085436A1 (en) * 2015-11-18 2017-05-26 Advanced Medical Solutions Limited Gelling fibres
CN106894111A (en) * 2017-03-30 2017-06-27 广东泰宝医疗科技股份有限公司 A kind of preparation method of the compound alginate dressing of soft moisture absorption

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103060946A (en) * 2012-12-21 2013-04-24 稳健实业(深圳)有限公司 Blend fibers of alginate and sodium carboxymethyl cellulose and preparation method and application thereof
CN106702533A (en) * 2015-07-27 2017-05-24 吴玉松 High-strength alginate composite fiber, and preparation method and use thereof
WO2017085436A1 (en) * 2015-11-18 2017-05-26 Advanced Medical Solutions Limited Gelling fibres
CN105544002A (en) * 2015-12-18 2016-05-04 厦门百美特生物材料科技有限公司 Superabsorbent composite fiber and preparation method thereof
CN106894111A (en) * 2017-03-30 2017-06-27 广东泰宝医疗科技股份有限公司 A kind of preparation method of the compound alginate dressing of soft moisture absorption

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108914389A (en) * 2018-07-11 2018-11-30 高昕文 A kind of preparation method of composite fiber spunlace mask base cloth
CN109137502A (en) * 2018-08-07 2019-01-04 苏州市天翱特种织绣有限公司 A kind of preparation method of moisture absorbing and sweat releasing knitting fabric
CN109627498A (en) * 2018-11-27 2019-04-16 青岛大学 A kind of sodium alginate-cellulose derivative blended membrane/fiber and preparation method thereof
CN109868525A (en) * 2019-02-19 2019-06-11 青岛海赛尔新材料科技有限公司 A kind of preparation method of high intensity seaweed and polyvinyl alcohol blending fiber
CN109972233A (en) * 2019-02-19 2019-07-05 青岛大学 Preparation method of biodegradable alginate fiber with high strength and high toughness
CN110241481A (en) * 2019-05-28 2019-09-17 福建美可纸业有限公司 A kind of superabsorbent water composite fibre and preparation method thereof
CN112127009A (en) * 2020-09-11 2020-12-25 嘉兴学院 Cellulose/calcium alginate blend fiber with skin-core structure and preparation method thereof
CN112127009B (en) * 2020-09-11 2022-10-14 嘉兴学院 Cellulose/calcium alginate blend fiber with skin-core structure and preparation method thereof
CN116730691A (en) * 2023-05-25 2023-09-12 东莞市欧丽亚环保材料有限公司 Ceramic tile adhesive and preparation method

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