WO2006002572A1 - Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci - Google Patents

Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci Download PDF

Info

Publication number
WO2006002572A1
WO2006002572A1 PCT/CN2004/000711 CN2004000711W WO2006002572A1 WO 2006002572 A1 WO2006002572 A1 WO 2006002572A1 CN 2004000711 W CN2004000711 W CN 2004000711W WO 2006002572 A1 WO2006002572 A1 WO 2006002572A1
Authority
WO
WIPO (PCT)
Prior art keywords
protein
spinning
hours
temperature
solution
Prior art date
Application number
PCT/CN2004/000711
Other languages
English (en)
Chinese (zh)
Inventor
Guanqi Li
Original Assignee
Guanqi Li
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Guanqi Li filed Critical Guanqi Li
Priority to PCT/CN2004/000711 priority Critical patent/WO2006002572A1/fr
Publication of WO2006002572A1 publication Critical patent/WO2006002572A1/fr

Links

Classifications

    • 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
    • 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
    • D01F8/04Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/10Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained by reactions only involving carbon-to-carbon unsaturated bonds as constituent

Definitions

  • the present invention relates to the field of textiles, and more particularly to a synthetic fiber containing proteins extracted from animal hair, and a method of producing such a synthetic fiber. Background technique
  • An object of the present invention is to provide a fiber for animal hair protein containing a wider range of uses and to provide a method for producing the same.
  • a synthetic fiber containing animal hair protein consisting of protein and polyvinyl alcohol, the protein is isolated protein extracted from animal hair, and the protein content in the fiber It is from 1% to less than 25% or from more than 40% to 90%.
  • the fiber has a protein content of 3% to 20%.
  • the protein has a protein content of 45% to 90%.
  • the method of making the synthetic fiber is:
  • the isolated protein is dissolved in an aqueous solution containing sodium dodecyl sulfate or triethanolamine, the dissolution temperature is 15 ° C - 95 ° C, and the dissolution time is 1. 5 - 4 hours to prepare a protein solution;
  • the water-washed polyvinyl alcohol is directly added to the protein solution, and they are blended and copolymerized at a temperature of 60 Torr to 98 ° C for a period of 1.5 to 4 hours, and the concentration of the protein-containing and polyvinyl alcohol is 8 %- 14% or 15%-38% spinning solution;
  • Spinning stock solution at a temperature of 50-80 ° (at room temperature, defoaming for 3-8 hours, or at a temperature of 30-40 ° C, vacuum degassing for 3-8 hours, into the spinning process, made into protein Synthetic fiber.
  • the animal hair When extracting protein from animal hair, the animal hair should be degreased and then immersed in an acidic solution at a temperature of 20-90 ° C for 1-8 hours. Separate and purify the waste residue, adjust the isoelectric point of the leachate with alkali, and extract. Protein is separated.
  • the protein synthetic fiber After entering the spinning process, the protein synthetic fiber can be formed by a wet spinning process.
  • the concentration of protein and polyvinyl alcohol in the spinning solution is 15% to 38.
  • the protein synthetic fiber can also be produced by a dry-jet wet spinning process.
  • the concentration of protein and polyethylene glycol in the spinning solution is 20% to 38%. After the spinning process, the dry spinning process can also be used to form the protein synthetic fiber.
  • the present invention not only uses animal hair as a raw material for producing protein, but also uses human broken hair as a raw material for producing protein, which further expands the source of raw materials for fiber production and makes full use of waste.
  • the fiber of the present invention when the content of the protein is low, since the polyvinyl alcohol content is high, and the instability of the SH-based gas-based acid is avoided, the produced fiber is not only elastic, hygroscopic, and gas permeable. Good characteristics, and good strength, can be spun into finer fibers to make the fabric softer.
  • the fiber is made to have better elasticity and skin-friendly properties. This fiber has the natural hemp fiber permeability, is not only comfortable to wear, but also an excellent material for making artificial wigs.
  • Inventions have opened up a broader avenue for the use of resources.
  • the spinning solution is prepared, the separated protein is dissolved in the near-neutral aqueous solution of triethanolamine or sodium dodecylsulfonate, and the polyvinyl alcohol is directly added to the protein solution, so that the produced fiber does not contain no Necessary inorganic chemical composition, and no pollution to the environment during the manufacturing process.
  • Example 1 The animal hair was degreased and then immersed in an aqueous solution having a pH of 1.5, and stirred. After 6 hours at a temperature of 70 Torr, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leaching solution was adjusted with a base to obtain a separation.
  • Protein the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, the dissolution temperature is 15 ° C, the dissolution time is 4 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein.
  • a spinning solution containing protein and polyvinyl alcohol at a concentration of 14%, wherein the protein
  • the weight ratio of dry solid to polyvinyl alcohol is 3:97; the boric acid is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is degassed under vacuum for 8 hours at a temperature of 30 ° C.
  • a protein synthetic fiber is produced by a wet spinning process.
  • Example 2 The animal hair was degreased and then immersed in an aqueous solution of pH 2, and stirred. After 7 hours at a temperature of 40 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base to obtain a separation.
  • Protein the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfonate, the dissolution temperature is 30 ° C, the dissolution time is 2 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein ⁇ In the solution, they were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 3.5 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 27%, wherein The dry weight ratio of protein shield and polyvinyl alcohol is 60: 40; boric acid is added to the spinning solution to adjust the viscosity to make a spinning dope; the spinning dope is allowed to defoam at a temperature of 4 G ° C under vacuum. After 4 hours, the spinning process was carried out, and the protein synthetic fiber was prepared by a wet spinning process.
  • Example 3 The human hair is degreased and then immersed in an aqueous solution having a pH of 2.3, and stirred. After 4 hours at a temperature of 90 ° C, the separation and purification are carried out to remove the waste residue, and the isoelectric point of the leaching solution is adjusted with a base to obtain a protein for human hair separation; the separated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, and the dissolution temperature is 60. 5 ⁇ The temperature is slowly increased to 98 ° C, maintaining 2.
  • the temperature is slowly increased to 98 ° C, the temperature is slowly increased to 98 ° C, kept for 2.5 hours , adding soft water to adjust the concentration, to obtain a spinning solution containing 38% of protein and polyvinyl alcohol, wherein the dry weight ratio of protein to polyvinyl alcohol is 45: 55; adding boric acid to the spinning solution
  • the viscosity is made into a spinning dope; the spinning dope is degassed at a temperature of 35 ° C under vacuum for 3 hours, and enters a spinning process to form a protein shield synthetic fiber by a wet spinning process.
  • Example 4 The animal hair and the human hair were degreased, and then immersed in an aqueous solution having a pH of 2.6 and stirred. After 8 hours at a temperature of 20 ° C, the separation and purification were carried out to remove the residue, and the leaching solution was adjusted with a base. The isoelectric point, the protein is separated; the separated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, the dissolution temperature is 50 ⁇ , the dissolution time is 3.8 hours, and the protein solution is prepared; The polyvinyl alcohol was directly added to the protein solution, and they were blended and copolymerized.
  • the temperature was slowly raised to 98 ° C for 4 hours, and soft water was added thereto to adjust the concentration to obtain a protein-containing and polyvinyl alcohol concentration of 8%.
  • a silk solution wherein the dry weight ratio of protein to polyvinyl alcohol is 1:99; boric acid is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to stand at a temperature of 38 ° C under vacuum After defoaming for 5. 5 hours, the spinning process was carried out, and the protein synthetic fiber was prepared by a wet spinning process.
  • Example 5 The animal hair was degreased and then immersed in an aqueous solution of pH 3, and stirred. After 1 hour at a temperature of 98 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base to obtain a separation.
  • Protein Shield The isolated protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 25 ° C, the dissolution time is 3.5 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein solution.
  • Example 6 The animal hair was degreased and then immersed in an aqueous solution having a pH of 1.1, and stirred. After 5 hours at a temperature of 30 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base.
  • the weight ratio of protein shield and polyvinyl alcohol is 40: 60; Boron solution is added to the spinning solution to form a spinning dope; the spinning dope is at a temperature of 80 ° (:, under normal pressure) The foaming was carried out for 5 hours, and the spinning process was carried out to prepare a protein synthetic fiber by a wet spinning process.
  • Example 7 The animal hair was degreased and then immersed in an aqueous solution of pH 1 and stirred. After 3 hours at a temperature of 80 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leaching solution was used to separate.
  • the protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 85 ° C, the dissolution time is 1.8 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein solution, They were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 2.8 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 15%, wherein protein and polyethylene.
  • the dry weight ratio of alcohol is 75: 25; 'The borax is added to the spinning solution to adjust the viscosity to make the spinning dope; the spinning dope is allowed to defoam at a temperature of 65 °C for 6 hours under normal pressure.
  • Silk process a protein synthetic fiber is produced by a wet spinning process.
  • Example 8 The animal hair was degreased and then immersed in an aqueous solution having a pH of 0.5, and stirred. After 2 hours at a temperature of 60 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base.
  • the protein is separated; the isolated protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 40 ° C, and the dissolution time is 3 hours to prepare a protein solution; a certain amount of washed pure polyvinyl alcohol is directly added to the protein solution, They are blended and copolymerized, and the temperature is slowly raised to 98 °C, keeping 3 small At the same time, adding soft water to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 11%, wherein the dry weight ratio of protein to polyvinyl alcohol is 90: 10; adding borax to the spinning solution The viscosity is adjusted to prepare a spinning dope; the spinning dope is allowed to defoam for 5 hours at a temperature of 75 ° C under normal pressure, and is subjected to a spinning process to form a protein synthetic fiber by a wet spinning process.
  • Example 9 The animal hair was degreased and then immersed in an aqueous solution having a pH of 0.7, and stirred, and after 25 hours at a temperature of 25 Torr, the separation and purification were carried out except that the waste was removed, and the leaching solution was adjusted with alkali.
  • the separation protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfonate, the dissolution temperature is 20 ° C, the dissolution time is 3.5 hours, and the protein solution is prepared; Vinyl alcohol was directly added to the protein solution, and they were blended and copolymerized.
  • the temperature was slowly raised to 98 ° C for 4 hours, and soft water was added thereto to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 15%.
  • the dry weight ratio of protein to polyvinyl alcohol is 15: 85; boric acid is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to defoam at a temperature of 30 ° C under vacuum. 7. 5 hours, into the spinning process, using a dry spray wet spinning process to make protein synthetic fibers.
  • Example 10 The animal hair was degreased and then immersed in an aqueous solution having a pH of 0.9, and stirred. After the temperature was 95 ° C for 1.5 hours, the separation and purification were carried out to remove the waste residue, and the alkali was used to adjust the isoelectricity of the leachate. Point, the protein is separated; the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, the dissolution temperature is 35 ° C, the dissolution time is 4 hours, and the protein solution is prepared; the pure polyethylene is washed with a certain amount of water. The alcohol was directly added to the protein solution, and they were blended and copolymerized.
  • the temperature was slowly raised to 98 ° C for 2 hours, and soft water was added thereto to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 16%.
  • the dry weight ratio of protein to polyvinyl alcohol is 70: 30; boric acid is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to defoam at a temperature of 40 ° C under vacuum conditions. After hours, enter the spinning process and make a protein synthetic fiber by dry-jet wet spinning.
  • Example 11 The human hair was degreased and then immersed in an aqueous solution having a pH of 2.8, and stirred. After 2 hours at a temperature of 98 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leaching solution was adjusted with a base.
  • the human hair is isolated; the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, dissolved The temperature was 70 ° C, the dissolution time was 3 hours, and the protein solution was prepared. A certain amount of washed pure polyethylene glycol was directly added to the protein solution, and they were blended and copolymerized, and the temperature was slowly raised to 98 ° C, and kept at 1.5.
  • Example 12 After the animal hair and the human hair were degreased, they were immersed in an aqueous solution of pH 3 and stirred, and after 3 hours at a temperature of 75 ° C, the separation and purification were carried out to remove the waste residue, and the alkali leaching solution was adjusted. The electric point is obtained by separating the protein shield; the separated protein is dissolved in a soft aqueous solution containing sodium dodecylsulfonate, the dissolution temperature is 80 ° C, the dissolution time is 1.5 hours, and the protein solution is prepared; The polyvinyl alcohol was directly added to the protein solution, and they were blended and copolymerized.
  • the temperature was slowly raised to 98 ° C for 3 hours, and soft water was added thereto to adjust the concentration to obtain a spinning concentration of 25% containing protein and polyvinyl alcohol.
  • Solution wherein the dry weight ratio of protein to polyethylene glycol is 12: 88; adding boric acid to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to stand at a temperature of 33 ° C under vacuum After defoaming for 3.5 hours, the spinning process was carried out, and the protein synthetic fiber was prepared by a dry-jet wet spinning process.
  • Example 13 The animal hair was degreased and then immersed in an aqueous solution of pH 1.3, and stirred. After 2.5 hours at a temperature of 85 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base to obtain a separation.
  • Protein the isolated protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 55 ° C, the dissolution time is 2 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein solution, so that They were blended and copolymerized, and the temperature was slowly raised to 98 Torr for 2.5 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 29%, wherein the dry weight of protein and polyvinyl alcohol The weight ratio is 80: 20; borax is added to the spinning solution to adjust the viscosity to make a spinning dope; the spinning dope is allowed to defoam for 8 hours at a temperature of 5 G ° (at normal pressure, into the spinning process, with dry spray) The wet spinning process produces protein synthetic fibers.
  • Example 14 The animal hair was degreased and then immersed in an aqueous solution having a pH of 1.8, and stirred, and after 5 hours at a temperature of 55 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectricity of the reduced leaching solution was used.
  • the protein is separated; the isolated protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 45 ° C, the dissolution time is 3.2 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added In the protein solution, they were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 1.8 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing 32% of protein and polyvinyl alcohol.
  • the dry weight ratio of protein to polyvinyl alcohol is 55: 45; borax is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to defoam at a temperature of 80 ° C under normal pressure. After 5 hours, enter the spinning process and make a protein synthetic fiber by dry-jet wet spinning.
  • Example 15 The animal hair was degreased and then immersed in an aqueous solution having a pH of 2.1, and stirred, and after 6 hours at a temperature of 35 ° C, the separation and purification were carried out to remove the waste residue, and the alkali was used to adjust the isoelectricity of the leachate.
  • the protein is separated; the isolated protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 65 ° C, the dissolution time is 2.5 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added In the protein solution, they were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 3 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 35%, in which protein and The sufficiency of the sulphide is 5. 5 hours.
  • the spinning solution is placed at a temperature of 65 ° C. , into the spinning process, using dry-jet wet spinning process to make protein synthetic fibers.
  • Example 17 The animal hair was degreased and then immersed in an aqueous solution having a pH of 1.5, and stirred. After 6 hours at a temperature of 70 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base. The protein is separated; the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulphate, the dissolution temperature is 15 ° C, the dissolution time is 4 hours, and a protein solution is prepared; a certain amount of water is washed directly with the pure polyvinyl alcohol.
  • the temperature is slowly raised to 98 ° C, and kept for 3.5 hours, during which soft water is added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 20%.
  • the dry weight ratio of protein to polyvinyl alcohol is 85: 15; boric acid is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to defoam at a temperature of 40 ° C under vacuum conditions. 5 hours, into the spinning process, using the dry spinning process to make protein synthetic fibers.
  • Example 18 Degrease the animal hair, and then immersed in an aqueous solution of pH 2, and stirred. After 7 hours at a temperature of 40 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base to obtain a separation.
  • Protein the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, the dissolution temperature is 30 ° C, the dissolution time is 2 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein In the solution, they were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 4 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing 38% of protein and polyvinyl alcohol, in which protein and poly 5 ⁇ ,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,
  • Example 19 The human hair was degreased and then immersed in an aqueous solution having a pH of 2.3, and stirred. After 4 hours at a temperature of 90 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base.
  • the human protein is separated into a protein; the isolated protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, the dissolution temperature is 60 ° C, the dissolution time is 1.5 hours, and the protein solution is prepared; Polyvinyl alcohol is directly added to the protein solution, and they are blended and copolymerized, and the temperature is slowly raised to 98 ° C.
  • Example 20 After the animal hair and the human hair were degreased, they were immersed in an aqueous solution having a pH of 2.6 and stirred. After 8 hours at a temperature of 20 Torr, the separation and purification were carried out to remove the waste residue, and the leaching solution was adjusted with a base. The protein is separated into a protein; the dissolved protein is dissolved in a soft aqueous solution containing sodium dodecyl sulfate, the dissolution temperature is 50 ° C, the dissolution time is 3.8 hours, and the protein solution is prepared; The polyvinyl alcohol was directly added to the protein solution, and they were blended and copolymerized.
  • the temperature was slowly raised to 98 ° C for 1.5 hours, and soft water was added thereto to adjust the concentration to obtain a protein-containing and polyvinyl alcohol concentration of 31%.
  • the spinning solution wherein the dry weight ratio of protein to polyvinyl alcohol is 65: 35; adding boric acid to the spinning solution to adjust the viscosity to prepare a spinning dope; spinning dope at a temperature of 30 ° C under vacuum After standing defoaming for 5. 5 hours, the spinning process was carried out, and the protein shield synthetic fiber was prepared by a dry spinning process.
  • Example 21 The animal hair was degreased and then immersed in an aqueous solution of pH 3, and stirred. After 1 hour at a temperature of 98 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the immersion liquid was separated.
  • the protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 25 ° C, the dissolution time is 3.5 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein solution, They were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 2 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 36%, wherein protein and polyvinyl alcohol were used.
  • the dry weight ratio is 17: 83; borax is added to the spinning solution to adjust the viscosity to make a spinning dope; the spinning dope is allowed to defoam for 5 hours at a temperature of 80 ° C under normal pressure, and enters the spinning process.
  • the protein synthetic fiber is made by a dry spinning process.
  • Example 22 The animal hair was degreased and then immersed in an aqueous solution having a pH of 1.1, and stirred. After 5 hours at a temperature of 30 ° C, the separation and purification were carried out to remove the waste sputum, and the isoelectric point of the leaching solution was adjusted with alkali. , The protein is separated; the isolated protein is dissolved in a soft aqueous solution containing triethanolamine, and the dissolution temperature is
  • Example 23 Degrease the animal hair, and then immersed in an aqueous solution of pH 1 and stirred. After 3 hours at a temperature of 80 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leachate was adjusted with a base to obtain a separation.
  • Protein the isolated protein is dissolved in a soft aqueous solution containing triethanolamine, the dissolution temperature is 85 ° C, the dissolution time is 1, 8 hours, and the protein solution is prepared; a certain amount of washed pure polyvinyl alcohol is directly added to the protein solution , they were blended and copolymerized, the temperature was slowly raised to 98 ° C, and maintained for 2.5 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 26%, in which protein and poly The dry weight ratio of vinyl alcohol is 38: 62; boron is added to the spinning solution to adjust the viscosity to prepare a spinning dope; the spinning dope is allowed to defoam for 8 hours at a temperature of 60 ° C under normal pressure. Spinning process, using a dry spinning process to make protein synthetic fibers.
  • Example 24 The animal hair was degreased and then immersed in an aqueous solution having a pH of 0.5, and stirred. After 2 hours at a temperature of 60 ° C, the separation and purification were carried out to remove the waste residue, and the isoelectric point of the leaching solution was adjusted with a base.
  • Separating the protein shield dissolving the isolated protein in a soft aqueous solution containing triethanolamine, dissolving at a temperature of 40 ° C, and dissolving for 3 hours to form a protein solution; adding a certain amount of washed pure polyvinyl alcohol directly to the protein solution , they were blended and copolymerized, and the temperature was slowly raised to 98 ° C for 3 hours, during which soft water was added to adjust the concentration to obtain a spinning solution containing protein and polyvinyl alcohol at a concentration of 34%, wherein protein and polyvinyl alcohol The dry weight ratio is 28: 72; borax is added to the spinning solution to adjust the viscosity to make a spinning dope; the spinning dope is allowed to defoam at a temperature of 50 ° C under normal pressure for 6 hours, and enters the spinning process.
  • a protein spinning synthetic fiber is produced by a dry spinning process.
  • the spinning process in the spinning process mentioned in the present invention is a prior art, and the inventors of the present invention are disclosed in the patent application file of the Chinese Patent No. 99116636.1 or 03111181.4 or 03111737. The process flow and parameters are not described in detail here.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Artificial Filaments (AREA)

Abstract

La présente invention concerne une fibre contenant une protéine dpoil animal. Cette fibre est composée d'une protéine séparéepoil d'un animal et d'un PVA. Dans cette fibre, la concentration de protéine est comprise entre 1 % et 25 % au maximum, u entre 40 % et 90 %. Cette invention concerne aussi le processus de production de cette fibre. Cette invention ne prend pas seulement un poil animal comme matières premières de protéine, mais égent un poil humain, ce qui permet d'étendre la ressource en atières premières pour la fabrication de cette fibre. En même tem la fibre obtenue ne contient pas de composants chimiques inorganiques inutiles et sa production n'apporte pas de pollution.
PCT/CN2004/000711 2004-06-30 2004-06-30 Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci WO2006002572A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/CN2004/000711 WO2006002572A1 (fr) 2004-06-30 2004-06-30 Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2004/000711 WO2006002572A1 (fr) 2004-06-30 2004-06-30 Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci

Publications (1)

Publication Number Publication Date
WO2006002572A1 true WO2006002572A1 (fr) 2006-01-12

Family

ID=35782457

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2004/000711 WO2006002572A1 (fr) 2004-06-30 2004-06-30 Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci

Country Status (1)

Country Link
WO (1) WO2006002572A1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008071062A1 (fr) 2006-12-12 2008-06-19 Hiking Group Co., Ltd Fibre de polyacrylonitrile modifiée, son procédé de préparation et son utilisation
WO2008071063A1 (fr) 2006-12-12 2008-06-19 Hiking Group Co., Ltd Fibre de polyacrylonitrile modifiée, son procédé de préparation et son utilisation
CN102154731A (zh) * 2011-01-26 2011-08-17 尹兆明 动物血液蛋白纤维及其制造方法
CN114737273A (zh) * 2021-01-07 2022-07-12 洛阳常龙新材料科技有限公司 一种离子液体溶解动物毛发及维尼纶的纺丝制胶方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10280278A (ja) * 1997-04-03 1998-10-20 Kuraray Co Ltd エチレン−ビニルアルコ−ル系共重合体繊維およびその製造方法
CN1376816A (zh) * 2002-04-15 2002-10-30 胡宗善 动物毛蛋白质再生纤维纺丝原液及其生产方法
CN1403643A (zh) * 2001-08-30 2003-03-19 陈福库 角蛋白复合纤维及其制造方法
CN1425813A (zh) * 2001-12-12 2003-06-25 中国科学院化学研究所 含动物蛋白质的合成纤维及其制备方法
CN1524980A (zh) * 2003-02-28 2004-09-01 李官奇 一种含有动物毛发蛋白质的合成纤维及其制造方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10280278A (ja) * 1997-04-03 1998-10-20 Kuraray Co Ltd エチレン−ビニルアルコ−ル系共重合体繊維およびその製造方法
CN1403643A (zh) * 2001-08-30 2003-03-19 陈福库 角蛋白复合纤维及其制造方法
CN1425813A (zh) * 2001-12-12 2003-06-25 中国科学院化学研究所 含动物蛋白质的合成纤维及其制备方法
CN1376816A (zh) * 2002-04-15 2002-10-30 胡宗善 动物毛蛋白质再生纤维纺丝原液及其生产方法
CN1524980A (zh) * 2003-02-28 2004-09-01 李官奇 一种含有动物毛发蛋白质的合成纤维及其制造方法

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008071062A1 (fr) 2006-12-12 2008-06-19 Hiking Group Co., Ltd Fibre de polyacrylonitrile modifiée, son procédé de préparation et son utilisation
WO2008071063A1 (fr) 2006-12-12 2008-06-19 Hiking Group Co., Ltd Fibre de polyacrylonitrile modifiée, son procédé de préparation et son utilisation
CN102154731A (zh) * 2011-01-26 2011-08-17 尹兆明 动物血液蛋白纤维及其制造方法
CN114737273A (zh) * 2021-01-07 2022-07-12 洛阳常龙新材料科技有限公司 一种离子液体溶解动物毛发及维尼纶的纺丝制胶方法

Similar Documents

Publication Publication Date Title
CN102733001B (zh) 一种羽毛蛋白纤维及其制备方法
CN103173892B (zh) 一种纳米竹纤维复合材料的制备方法
CN101654813A (zh) 蛋白质与海藻酸盐复合纤维及其制造方法
CN110952159B (zh) 一种蚕丝丝素蛋白溶液在再生纤维素纤维制备中的应用
CN109181451B (zh) 一种聚丙烯酸酯/MOFs复合皮革涂饰剂的制备方法
WO2006002572A1 (fr) Fibre synthetique contenant une proteine de poil animal et preparation de celle-ci
CN103835023B (zh) 一种甲醇蛋白改性再生纤维素纤维及其生产工艺
CN114318572A (zh) 一种蛋白纤维及其制备方法
CN104353372A (zh) 一种芳香族聚酰胺中空纤维多孔膜的制备方法
CN103816817A (zh) 一种耐碱纤维素膜及其制备方法
CN1425813A (zh) 含动物蛋白质的合成纤维及其制备方法
CN104928792A (zh) 一种防静电的羽绒复合纤维
CN108624974B (zh) 一种珍珠纤维的制备方法
CN110283349A (zh) 一种木质素磺酸盐纤维素复合膜的制备方法
CN102534859B (zh) 一种大豆蛋白质与聚乙烯醇聚合纤维的制造方法
CN107502982B (zh) 一种羽毛角蛋白粘胶纤维的制备方法
CN102839441B (zh) 一种高弹角蛋白再生纤维及其制备方法
CN106948027A (zh) 一种小麦蛋白纤维的制备方法
CN1217041C (zh) 一种蛋白质合成纤维及其制造方法
CN105951212A (zh) 一种含孔雀毛的空气感人造假发纤维
CN108816062A (zh) 聚酰胺-海藻纤维透析膜及其制备方法
CN1245542C (zh) 一种含有动物毛发蛋白质的合成纤维及其制造方法
CN105002591B (zh) 一种用鹌鹑羽毛制备发用复合纤维的方法
CN105133056A (zh) 一种隔音保暖性好的新型复合纤维纺织材料
CN112876711B (zh) 一种高强度丝蛋白纳米纤维膜及其制备方法

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

32PN Ep: public notification in the ep bulletin as address of the adressee cannot be established

Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 69(1) EPC, 1205A DATED 16.03.2007.

122 Ep: pct application non-entry in european phase