CN114381103A - Environment-friendly antibacterial foreign language translator material and preparation method thereof - Google Patents

Environment-friendly antibacterial foreign language translator material and preparation method thereof Download PDF

Info

Publication number
CN114381103A
CN114381103A CN202210133655.0A CN202210133655A CN114381103A CN 114381103 A CN114381103 A CN 114381103A CN 202210133655 A CN202210133655 A CN 202210133655A CN 114381103 A CN114381103 A CN 114381103A
Authority
CN
China
Prior art keywords
foreign language
language translator
antibacterial
polylactic acid
melting
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
Application number
CN202210133655.0A
Other languages
Chinese (zh)
Inventor
张晓雯
谈鑫
王雨静
殷嘉澳
孙建光
李梓
夏木建
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Huaiyin Institute of Technology
Original Assignee
Huaiyin Institute of Technology
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 Huaiyin Institute of Technology filed Critical Huaiyin Institute of Technology
Priority to CN202210133655.0A priority Critical patent/CN114381103A/en
Publication of CN114381103A publication Critical patent/CN114381103A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/12Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
    • C08J9/122Hydrogen, oxygen, CO2, nitrogen or noble gases
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0061Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/009Use of pretreated compounding ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00Foams characterized by the expanding agent
    • C08J2203/06CO2, N2 or noble gases
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00Foams characterized by the expanding agent
    • C08J2203/08Supercritical fluid
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/04Polyesters derived from hydroxy carboxylic acids, e.g. lactones
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2405/00Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2401/00 or C08J2403/00
    • C08J2405/08Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0806Silver
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/12Adsorbed ingredients, e.g. ingredients on carriers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Biological Depolymerization Polymers (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

The invention discloses an environment-friendly antibacterial foreign language translator material and a preparation method thereof. The preparation method comprises the following steps: mixing the chitosan solution with the silver nitrate solution, and obtaining the chitosan antibacterial fiber loaded with the nano Ag particles through visible light irradiation and electrostatic spinning processes; heating and melting polylactic acid to extrude a hollow polylactic acid wire; guiding the three-dimensional model of the foreign language translator into a fused deposition modeling device for layering and slicing; and (2) putting the chitosan antibacterial fiber into a hollow polylactic acid wire hole, heating and melting to form a melt, introducing critical inert gas, maintaining the pressure to dissolve the inert gas into the melt, forming a foreign language translator structure by melting and depositing the melt, and performing in-situ micropore foaming to form a micropore structure in the processes of cooling and solidification at room temperature and pressure release to obtain the chitosan antibacterial fiber. The invention realizes the preparation of the foreign language translator material with dual functions of environmental protection, degradability and long-acting antibiosis, and has wide application prospect.

Description

Environment-friendly antibacterial foreign language translator material and preparation method thereof
Technical Field
The invention relates to a functional environment-friendly material and a preparation method thereof, in particular to an environment-friendly antibacterial foreign language translator material and a preparation method thereof.
Background
The language is an important tool for expressing emotion and demand, and with the acceleration of the globalization process, the communication and communication demands among people in different countries are increased rapidly, but due to the difference of languages in different countries, the difficulty in mastering various languages by individuals is high, and the communication among people in different countries is limited. The foreign language translator can realize a translation tool for translating multiple languages, and the generation of the translation tool can solve the problems.
At present, most foreign language translator shells in the market are made of light non-degradable plastics such as ABS, PC and the like, and upgrading and elimination of the foreign language translator shells inevitably bring more environmental pollution, for example, the foreign language translator shells are buried in soil to influence crops to absorb nutrients and moisture, so that the yield of the crops is reduced, underground water sources are polluted, and harmful gas, polluted air and the like are generated by burning; on the other hand, because the foreign language translator is used in different public places for a long time, even if the foreign language translator is disinfected before being used every time, the foreign language translator cannot avoid adhesion and proliferation of bacteria and even can become a carrier for pathogen transmission, and the foreign language translator is required to be kept close to the nose and the mouth of a person in the using process, so that the health of the user is harmed.
Disclosure of Invention
The purpose of the invention is as follows: the invention aims to provide an environment-friendly antibacterial foreign language translator material with dual functions of environment protection, degradability and long-acting antibiosis;
the second purpose of the invention is to provide a preparation method of the environment-friendly antibacterial foreign language translator material.
The technical scheme is as follows: the environment-friendly antibacterial foreign language translator material comprises chitosan/polylactic acid with a microporous structure loaded with antibacterial nano Ag particles.
Wherein the nano Ag particles have the particle size of 3-10 nm and the content of 0.1-0.3 wt.%.
Wherein the pore diameter of the microporous structure is 10-80 μm.
The preparation method of the environment-friendly antibacterial foreign language translator material comprises the following steps:
(1) mixing chitosan solution with silver nitrate solution, and irradiating with visible light to promote Ag in spinning process+Reducing the nano Ag in situ to obtain the chitosan antibacterial fiber loaded with nano Ag particles;
(2) heating and melting biodegradable polylactic acid, and extruding a hollow polylactic acid wire;
(3) guiding the three-dimensional model of the foreign language translator into a fused deposition forming device, and slicing in layers;
(4) putting the chitosan antibacterial fiber loaded with the nano Ag particles into a hollow polylactic acid wire hole, heating and melting the chitosan antibacterial fiber in a melting deposition forming device to form a melt, introducing critical inert gas, maintaining the pressure to promote the inert gas to be dissolved in the melt, forming the foreign language translator structure by melting deposition of the melt, and performing in-situ micropore foaming to form a micropore structure in the processes of cooling solidification and pressure release to prepare the environment-friendly antibacterial foreign language translator material.
The environment-friendly antibacterial foreign language translator material is a microporous structure chitosan/polylactic acid antibacterial foreign language translator material loaded with antibacterial nano Ag particles.
Wherein, in the step (1), the silver nitrate solution is added into the chitosan solution and then stirred, the visible light irradiation is adopted to assist the electrostatic spinning process, and the visible light irradiation promotes Ag in the spinning process+In situ reduction to nanoAg; extruding the hollow polylactic acid wire material by an extrusion molding process in the step (2); and (4) heating the hollow polylactic acid wire material in a melting cavity of a fused deposition forming device until the hollow polylactic acid wire material is melted into a melt, introducing critical inert gas into the melting cavity, maintaining the pressure, promoting the inert gas to be dissolved in the melt, forming the foreign language translator structure by fused deposition, and performing in-situ micropore foaming to form a micropore structure in the processes of cooling solidification at room temperature and pressure release to obtain the environment-friendly antibacterial foreign language translator material.
Wherein, in the step (4), the critical inert gas is one or more of carbon dioxide, nitrogen, argon, helium and ethane.
In the step (4), the pressure of the melting cavity is maintained at 3-12 MPa for 5-20 s. Under the pressure and time, the critical inert gas is fully dissolved in the melt.
In the step (4), the concentration of the critical inert gas introduced into the melting cavity is 0.5-1.5 mol/L. At this concentration, the critical inert gas can be uniformly dissolved in the melt.
In the step (4), the volume ratio of the critical inert gas introduced into the melting cavity to the hollow polylactic acid wire is 1: 3-1: 10. At this ratio, the pore size of the micropores can be effectively controlled after the inert gas is released.
Wherein in the step (1), the voltage of the electrostatic spinning process is 15-18 kV.
In the step (1), chitosan is dissolved in a mixed aqueous solution of 3.5-4 wt.% of acetic acid and 0.5-1 wt.% of ethylenediamine, and the mixture is stirred to obtain a chitosan solution.
Wherein in the step (2), the spinning aperture of the hollow polylactic acid filament is 0.1-0.2 mm.
The invention principle is as follows: according to the requirements of environmental protection and antibacterial function of foreign language translator materials, based on the biodegradation characteristic of polylactic acid and the antibacterial function of Ag/chitosan, a visible light irradiation auxiliary electrostatic spinning process is designed, the irradiation of visible light in the electrostatic spinning process promotes the in-situ synthesis of nano Ag particles, and the chitosan antibacterial fiber loaded with nano Ag particles is obtained; the biodegradable polylactic acid is heated and melted and then extruded out of a hollow wire material, a critical inert gas-based auxiliary melting deposition process is designed, chitosan antibacterial fiber loaded with nano Ag particles is placed into the hollow polylactic acid wire material, the hollow polylactic acid wire material is melted into a melt by a melting deposition forming machine and then is pressurized, critical carbon dioxide is introduced to promote the critical inert gas to be dissolved into the melt, after the hollow polylactic acid wire material is formed by the melting deposition process, in-situ micropore foaming is carried out in the processes of room temperature cooling solidification and pressure release to form a micropore structure, the antibacterial nano Ag particles loaded in the micropore structure are continuously released, the lasting antibacterial function can be realized, and the polylactic acid is biodegradable and is convenient to recover and environment-friendly.
Has the advantages that: compared with the prior art, the invention has the following remarkable advantages:
(1) based on the electrostatic spinning principle and the illumination radiation reduction mechanism, the visible light radiation-assisted electrostatic spinning process is designed, namely, the silver nitrate-doped polylactic acid solution applies visible light radiation in the electrostatic spinning process to promote Ag+Is reduced into nano Ag particles and is loaded in the polylactic acid antibacterial fiber in situ, so that the interface bonding strength between the nano antibacterial particles and the polylactic acid fiber can be obviously enhanced, and the antibacterial long-acting property is favorably improved.
(2) Based on a fused deposition forming principle and the characteristics of critical inert gas, a critical inert gas-assisted fused deposition process is designed, chitosan antibacterial fiber/polylactic acid loaded with nano Ag particles is heated and melted into a melt by a fused deposition forming machine, pressure is maintained, the critical inert gas is introduced to promote the inert gas to be dissolved in the melt, and after the forming is carried out according to a foreign language translator model, in-situ foaming is induced in the processes of room temperature cooling solidification and pressure release to form micropores, so that the integrated manufacturing of a micropore structure/antibacterial function is realized.
(3) The chitosan/polylactic acid foreign language translator material with the microporous structure loaded with antibacterial nano Ag particles is newly designed for the requirements of environmental protection and antibacterial function of foreign language translator materials, and the antibacterial function and the recovery environmental protection effect of the chitosan/polylactic acid foreign language translator material are realized.
(4) According to the physical properties of carbon dioxide and other inert gases, the mixed gas of carbon dioxide and other inert gases is innovatively designed to be used as an auxiliary gas source so as to reduce the critical pressure, reduce the required critical pressure, effectively reduce the energy consumption, reduce the requirement on critical inert gas auxiliary fused deposition process equipment, and have good economic value.
(5) The size of micron pores is reasonably regulated and controlled by controlling the concentration of the inert gas, and the porosity is regulated and controlled by the volume ratio of the inert gas to the hollow polylactic acid wire material, so that the hollow polylactic acid wire material has the advantages of large volume ratio, large porosity and low density.
Drawings
Fig. 1 is a partial porous morphology diagram of the environmentally-friendly antibacterial foreign language translator material prepared in example 1.
Detailed Description
The present invention is described in further detail below.
Example 1
(1) Dissolving chitosan in a mixed aqueous solution of 4 wt.% acetic acid and 1 wt.% ethylenediamine, stirring, adding 0.2g/L diluted silver nitrate solution, stirring, and performing visible light irradiation assisted electrostatic spinning with spinning pore diameter of 0.1mm and voltage of 15kV to promote Ag in the spinning process+Reducing the nano Ag in situ to obtain the chitosan antibacterial fiber loaded with nano Ag particles;
(2) heating the biodegradable polylactic acid to 180 ℃ for melting, and extruding a hollow wire material by an extrusion molding process;
(3) introducing the three-dimensional model of the foreign language translator into a fused deposition forming machine, and carrying out layered slicing treatment;
(4) putting the chitosan antibacterial fiber loaded with the nano Ag particles in the step (1) into the holes of the hollow polylactic acid wire in the step (2), feeding the wire material into a melting cavity through a wire feeding device of a fused deposition forming machine, heating the wire material until the wire material is completely melted into a melt, setting the pressure in the melting cavity to be 3MPa, introducing 0.5mol/L critical carbon dioxide gas, and the volume ratio of the gas to the hollow polylactic acid wire is 1:3, and the melt is subjected to pressure maintaining for 5s to promote the carbon dioxide to be dissolved in the melt, then the melt is melted and deposited layer by track through an extrusion head of a melting and depositing forming machine to form a foreign language translator structure, and carrying out in-situ micropore foaming to form a micropore structure in the processes of cooling solidification at room temperature and pressure release to obtain the chitosan/polylactic acid material foreign language translator with the micropore structure loaded with the antibacterial nano Ag particles.
Fig. 1 is a pore morphology diagram of the material for the environmentally-friendly antibacterial foreign language translator prepared in example 1, and it can be found that the size of pores is in the micrometer/nanometer dual-scale range, the specific surface area is large, the action area of antibacterial particles is favorably enhanced, and the pores are in a nearly circular shape.
The in vitro antibacterial performance test is carried out on the environment-friendly antibacterial foreign language translator material formed in the embodiment, staphylococcus aureus is selected as a test object, the antibacterial performance of the foreign language translator material is detected according to QB/T2591-2003 'antibacterial plastic-antibacterial performance test method and antibacterial effect', the result shows that after the test is carried out for 24 hours, the antibacterial rate of the environment-friendly antibacterial foreign language translator material to staphylococcus aureus reaches 99.9%, the antibacterial rate after the test is carried out for 72 hours still reaches 99.8%, and the environment-friendly antibacterial foreign language translator material has good lasting antibacterial performance.
Example 2
(1) Dissolving chitosan in a mixed aqueous solution of 3.5 wt.% acetic acid and 0.5 wt.% ethylenediamine, stirring, adding 0.8g/L dilute silver nitrate solution, stirring, and performing visible light irradiation assisted electrostatic spinning with spinning pore diameter of 0.2mm and voltage of 16kV to promote Ag in the spinning process+Reducing the nano Ag in situ to obtain the chitosan antibacterial fiber loaded with nano Ag particles;
(2) heating the biodegradable polylactic acid to 180 ℃ for melting, and extruding a hollow wire material by an extrusion molding process;
(3) introducing the three-dimensional model of the foreign language translator into a fused deposition forming machine, and carrying out layered slicing treatment;
(4) putting the chitosan antibacterial fiber loaded with the nano Ag particles in the step (1) into the holes of the hollow polylactic acid wire in the step (2), feeding the wire material into a melting cavity through a wire feeding device of a fused deposition forming machine, heating the wire material until the wire material is completely melted into a melt, setting the pressure in the melting cavity to be 10MPa, introducing 1.0mol/L of mixed inert gas of critical carbon dioxide and argon, and the volume ratio of the gas to the hollow polylactic acid wire is 1:5, and the melt is subjected to pressure maintaining for 5s to promote the carbon dioxide to be dissolved in the melt, then the melt is melted and deposited layer by track through an extrusion head of a melting and depositing forming machine to form a foreign language translator structure, and carrying out in-situ micropore foaming to form a micropore structure in the processes of cooling solidification at room temperature and pressure release to obtain the chitosan/polylactic acid material foreign language translator with the micropore structure loaded with the antibacterial nano Ag particles.
The in vitro antibacterial performance test is carried out on the environment-friendly antibacterial foreign language translator material formed in the embodiment, staphylococcus aureus is selected as a test object, the antibacterial performance of the foreign language translator material is detected according to QB/T2591-2003 'antibacterial plastic-antibacterial performance test method and antibacterial effect', the result shows that after the test is carried out for 24 hours, the antibacterial rate of the environment-friendly antibacterial foreign language translator material to staphylococcus aureus reaches 99.98%, the antibacterial rate after the test is carried out for 72 hours still reaches 99.9%, and the environment-friendly antibacterial foreign language translator material has good lasting antibacterial performance.
Example 3
(1) Dissolving chitosan in a mixed aqueous solution of 3.5 wt.% acetic acid and 0.5 wt.% ethylenediamine, stirring, adding 0.8g/L dilute silver nitrate solution, stirring, and performing visible light irradiation assisted electrostatic spinning with spinning pore diameter of 0.2mm and voltage of 18kV to promote Ag in the spinning process+Reducing the nano Ag in situ to obtain the chitosan antibacterial fiber loaded with nano Ag particles;
(2) heating biodegradable polylactic acid to 190 ℃ for melting, and extruding a hollow wire material by an extrusion molding process;
(3) introducing the three-dimensional model of the foreign language translator into a fused deposition forming machine, and carrying out layered slicing treatment;
(4) putting the chitosan antibacterial fiber loaded with the nano Ag particles in the step (1) into the hollow polylactic acid wire hole in the step (2), feeding the wire into a melting cavity through a wire feeding device of a fused deposition forming machine, heating until the wire is completely melted into a melt, setting the pressure in the melting cavity to be 12MPa, introducing 1.5mol/L of inert gas mixed with critical carbon dioxide and helium, wherein the volume ratio of the gas to the hollow polylactic acid wire is 1:10, then gradually melting and depositing the melt layer by layer through an extrusion head of the fused deposition forming machine to form a foreign language translator structure, and carrying out in-situ micropore foaming to form a micropore structure in the processes of room temperature cooling solidification and pressure release to obtain the chitosan/polylactic acid material translator with the micropore structure loaded with the antibacterial nano Ag particles.
The in vitro antibacterial performance test is carried out on the environment-friendly antibacterial foreign language translator material formed in the embodiment, staphylococcus aureus is selected as a test object, the antibacterial performance of the foreign language translator material is detected according to QB/T2591-2003 'antibacterial plastic-antibacterial performance test method and antibacterial effect', the result shows that after the test is carried out for 24 hours, the antibacterial rate of the environment-friendly antibacterial foreign language translator material to staphylococcus aureus reaches 99.99%, and the antibacterial rate after the test is carried out for 72 hours still reaches 99.8%, so that the environment-friendly antibacterial foreign language translator material has good lasting antibacterial performance.
Example 4
The basic procedure was the same as in example 1, except that in the step (4), 0.8mol/L of critical carbon dioxide gas was introduced.
In example 4, the critical inert carbon dioxide gas has a high concentration and a high dispersion degree, the size of generated micropores is small, the action area of the antibacterial Ag particles is increased, and the bacteriostasis rate is increased to 99.95%.
Example 5
The basic procedure was the same as in example 1, except that in the step (4), the ratio of the volume of the critical carbon dioxide introduced into the melting chamber to the volume of the hollow polylactic acid wire was 1: 8.
In example 5, the ratio of the volume of carbon dioxide to the volume of the hollow polylactic acid wire material is increased, so that the porosity is increased, the content of the antibacterial Ag particles is reduced, and the antibacterial rate is slightly reduced to 99.91 percent.
Example 6
The basic procedure was the same as in example 1, except that in the step (4), 0.5mol/L of a mixed inert gas of critical carbon dioxide and argon was introduced.
In the embodiment 6, the critical carbon dioxide and the argon are used as the mixed inert gas, the pressure is reduced to 1.1MPa, the energy consumption is effectively reduced, and the service life of the equipment is prolonged.
Comparative example 1
The basic procedure was the same as in example 1, except that in step (4), the pressure of the melt chamber was maintained at 2MPa for 2 s.
Comparative example 2
The basic procedure was as in example 1, except that in the step (4), the critical inert carbon dioxide gas was introduced at a concentration of 0.1 mol/L.
Comparative example 3
The basic procedure was the same as in example 1, except that in the step (4), the ratio of the volume of the critical carbon dioxide introduced into the melting chamber to the volume of the hollow polylactic acid wire was 1: 2.
The in-vitro antibacterial performance test of the environment-friendly antibacterial foreign language translator material formed in the comparative examples 1-3 shows that the antibacterial rate of the environment-friendly antibacterial foreign language translator material to staphylococcus aureus is lower than 99% after the test is carried out for 24 hours. The pressure in the comparative example 1 is low, the inert carbon dioxide gas is difficult to reach a critical state, so that the inert carbon dioxide gas is difficult to dissolve in the melt, a microporous structure cannot be generated, the action area of the antibacterial Ag particles is reduced, and the bacteriostasis rate is reduced; in the comparative example 2, the concentration of the critical inert carbon dioxide gas is too low, and most of generated micropores are closed pores, so that the action area of the antibacterial Ag particles is sharply reduced, and the bacteriostasis rate is reduced; in comparative example 3, the volume ratio of the critical carbon dioxide is large, so that the pore size is increased, the mechanical strength is low, and the requirement on the use mechanical property is difficult to meet.

Claims (10)

1. An environment-friendly antibacterial foreign language translator material is characterized by comprising chitosan/polylactic acid with a microporous structure loaded with antibacterial nano Ag particles.
2. The environmentally friendly antibacterial foreign language translator material of claim 1, wherein the nano Ag particles have a particle size of 3 to 10nm and a content of 0.1 to 0.3 wt.%.
3. The environmentally friendly antibacterial foreign language translator material of claim 1, wherein the pore size of the microporous structure is 10 to 80 μm.
4. The method for preparing the environmentally friendly antibacterial foreign language translator material of claim 1, comprising the steps of:
(1) mixing chitosan solution with silver nitrate solution, and irradiating with visible light to promote Ag in spinning process+Reducing the nano Ag in situ to obtain the chitosan antibacterial fiber loaded with nano Ag particles;
(2) heating and melting biodegradable polylactic acid, and extruding a hollow polylactic acid wire;
(3) guiding the three-dimensional model of the foreign language translator into a fused deposition forming device, and slicing in layers;
(4) putting the chitosan antibacterial fiber loaded with the nano Ag particles into a hollow polylactic acid wire hole, heating and melting the chitosan antibacterial fiber in a melting deposition forming device to form a melt, introducing critical inert gas, maintaining the pressure to promote the inert gas to be dissolved in the melt, forming the foreign language translator structure by melting deposition of the melt, and performing in-situ micropore foaming to form a micropore structure in the processes of cooling solidification and pressure release to prepare the environment-friendly antibacterial foreign language translator material.
5. The method for manufacturing environmentally friendly antibacterial foreign language translator material according to claim 4, wherein in the step (4), the pressure of the melting chamber is maintained at 3 to 12MPa for 5 to 20 s.
6. The method for preparing environmentally friendly antibacterial foreign language translator material according to claim 4, wherein the critical inert gas in step (4) is at least one of carbon dioxide, nitrogen, argon, helium, and ethane.
7. The method for preparing environment-friendly antibacterial foreign language translator material according to claim 4, wherein in the step (4), the concentration of the critical inert gas introduced into the melting chamber is 0.5-1.5 mol/L.
8. The method for preparing environment-friendly antibacterial foreign language translator material according to claim 4, wherein in the step (4), the ratio of the volume of the critical inert gas introduced into the melting cavity to the volume of the hollow polylactic acid wire is 1: 3-1: 10.
9. The method for preparing environment-friendly antibacterial foreign language translator material according to claim 4, wherein in the step (1), the voltage of the electrostatic spinning process is 15-18 kV.
10. The method for preparing environment-friendly antibacterial foreign language translator material according to claim 4, wherein in the step (2), the spinning pore diameter of the hollow polylactic acid filament is 0.1-0.2 mm.
CN202210133655.0A 2022-02-14 2022-02-14 Environment-friendly antibacterial foreign language translator material and preparation method thereof Pending CN114381103A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202210133655.0A CN114381103A (en) 2022-02-14 2022-02-14 Environment-friendly antibacterial foreign language translator material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210133655.0A CN114381103A (en) 2022-02-14 2022-02-14 Environment-friendly antibacterial foreign language translator material and preparation method thereof

Publications (1)

Publication Number Publication Date
CN114381103A true CN114381103A (en) 2022-04-22

Family

ID=81206284

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202210133655.0A Pending CN114381103A (en) 2022-02-14 2022-02-14 Environment-friendly antibacterial foreign language translator material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN114381103A (en)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007277733A (en) * 2006-04-03 2007-10-25 Yyl:Kk Method for producing antibacterial/antiviral fiber and device for producing the same
CN101187111A (en) * 2007-11-29 2008-05-28 东华大学 Composite nanometer fiber felt containing nano silver gelatin/chitosan for medical dressing and its preparation
CN101297976A (en) * 2008-06-18 2008-11-05 天津大学 Preparation of antibacterial silver/chitosan nano fiber membrane
CN103320967A (en) * 2013-06-28 2013-09-25 陕西煤业化工技术研究院有限责任公司 Composite electrostatic spinning material containing fullerene and nano-silver for medical dressings and method for manufacturing composite electrostatic spinning material
CN103705969A (en) * 2014-01-02 2014-04-09 东华大学 Method for preparing chitosan-based silver-loaded composite antimicrobial superfine fiber membrane
CN106493968A (en) * 2016-12-15 2017-03-15 北京化工大学 A kind of method and device of the production foaming product that combines with 3D printing
CN106620813A (en) * 2016-12-26 2017-05-10 苏州大学 Preparation method of medical antibacterial nano dressing
CN109763185A (en) * 2018-12-14 2019-05-17 王惟正 One kind is for cigarette cooling filter hollow acid fiber by polylactic of section and preparation method thereof
US20190282968A1 (en) * 2016-05-11 2019-09-19 Guizhou Material Industrial Technology Institute Preparation method of high-strength anti-pollution antibacterial hollow fiber nanofiltration membrane and product
CN113235186A (en) * 2021-04-27 2021-08-10 河南银金达新材料股份有限公司 Preparation method of antibacterial polylactic acid nanofiber

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007277733A (en) * 2006-04-03 2007-10-25 Yyl:Kk Method for producing antibacterial/antiviral fiber and device for producing the same
CN101187111A (en) * 2007-11-29 2008-05-28 东华大学 Composite nanometer fiber felt containing nano silver gelatin/chitosan for medical dressing and its preparation
CN101297976A (en) * 2008-06-18 2008-11-05 天津大学 Preparation of antibacterial silver/chitosan nano fiber membrane
CN103320967A (en) * 2013-06-28 2013-09-25 陕西煤业化工技术研究院有限责任公司 Composite electrostatic spinning material containing fullerene and nano-silver for medical dressings and method for manufacturing composite electrostatic spinning material
CN103705969A (en) * 2014-01-02 2014-04-09 东华大学 Method for preparing chitosan-based silver-loaded composite antimicrobial superfine fiber membrane
US20190282968A1 (en) * 2016-05-11 2019-09-19 Guizhou Material Industrial Technology Institute Preparation method of high-strength anti-pollution antibacterial hollow fiber nanofiltration membrane and product
CN106493968A (en) * 2016-12-15 2017-03-15 北京化工大学 A kind of method and device of the production foaming product that combines with 3D printing
CN106620813A (en) * 2016-12-26 2017-05-10 苏州大学 Preparation method of medical antibacterial nano dressing
CN109763185A (en) * 2018-12-14 2019-05-17 王惟正 One kind is for cigarette cooling filter hollow acid fiber by polylactic of section and preparation method thereof
CN113235186A (en) * 2021-04-27 2021-08-10 河南银金达新材料股份有限公司 Preparation method of antibacterial polylactic acid nanofiber

Similar Documents

Publication Publication Date Title
US9656900B2 (en) Methods to fabricate nano-macro porous glass using a water soluble pore former
CN109825046B (en) Biodegradable polylactic acid foaming particle and preparation method thereof
CN107744601B (en) Three-dimensional printing wound coating material based on silk microsphere biological ink and preparation method thereof
CN102174717B (en) Microporous foaming polypropylene fiber and preparation method thereof
CN107041971A (en) A kind of fibroin based on 3 D-printing/gelatin timbering material and preparation method thereof
KR102012709B1 (en) Method for preparation of dual-pore scaffold for medical use by using FDM 3D printing
CN108727793B (en) Modified shaving board, reinforced polylactic acid 3D printing material and preparation method thereof
CN105566755A (en) Surface layer-core layer synchronous co-extrusion flame-retardant wood-plastic composite material and manufacturing method thereof
CN114381103A (en) Environment-friendly antibacterial foreign language translator material and preparation method thereof
KR20180089029A (en) The method of preparing wound dressing by 3-D printing and electro spinning technology
CN113599575A (en) Gradient density scaffold material and preparation method and application thereof
CN106752007B (en) Poly (propylene carbonate)/agriculture and forestry biomass composite material, preparation method and application
CN106552286B (en) The preparation method of artificial cartilage
KR101542919B1 (en) Eco-friendly composite polymer pellet having improved mechanical property, manufacturing method thereof, and fabric yarn using the same
CN104624128A (en) Special light microsphere for stone paper and preparation method of light microsphere
CN107353523A (en) A kind of water-soluble poval foam and preparation method thereof
CN107244058A (en) A kind of preparation method of waste material extrusion-blown modling
AU2001237404A1 (en) Method and device for extrusion-moulding of a hollow body made of thermoplastic material
KR102166991B1 (en) Method for controling pores in preparation of porous scaffold by FDM 3D printing
CN102442813A (en) Cotton stalk bark fiber reinforced gypsum composite material and preparation method thereof
CN105421042A (en) Light high-strength and high-toughness single green composite fiber and preparation method thereof
CN113735599A (en) Porous ceramic body, preparation method thereof and electronic cigarette applying porous ceramic body
JP4951761B2 (en) Biodegradable polymer film and method for producing the same
CN111334002B (en) Earplug manufacturing material and preparation method thereof
CN108513844B (en) Production and use method of one-way water seepage self-crushing mulching film

Legal Events

Date Code Title Description
PB01 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: 20220422

RJ01 Rejection of invention patent application after publication