CN113756126B - Aramid nanofiber, preparation method and application thereof, and preparation method of aramid paper - Google Patents
Aramid nanofiber, preparation method and application thereof, and preparation method of aramid paper Download PDFInfo
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- CN113756126B CN113756126B CN202111086169.XA CN202111086169A CN113756126B CN 113756126 B CN113756126 B CN 113756126B CN 202111086169 A CN202111086169 A CN 202111086169A CN 113756126 B CN113756126 B CN 113756126B
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H13/00—Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
- D21H13/10—Organic non-cellulose fibres
- D21H13/20—Organic non-cellulose fibres from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H13/26—Polyamides; Polyimides
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
- D01F6/605—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides from aromatic polyamides
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H15/00—Pulp or paper, comprising fibres or web-forming material characterised by features other than their chemical constitution
- D21H15/02—Pulp or paper, comprising fibres or web-forming material characterised by features other than their chemical constitution characterised by configuration
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Abstract
The invention provides aramid nano-fiber, a preparation method and application thereof, and a preparation method of aramid paper, wherein the preparation method of the aramid nano-fiber comprises the following steps: dispersing an aramid polymer into a first solvent to obtain an aramid polymer dispersion liquid; spraying the mixture into a second solvent after gas spray atomization treatment to obtain a dispersion liquid; then the superfine grain pulp is grinded. According to the preparation method, the aramid fiber polymer dispersion liquid is disordered and dispersed by using high-speed flowing compressed gas to obtain the aramid fiber micro-nanofiber dispersion liquid, the aramid fiber polymer arrangement structure is regulated and controlled by adjusting the concentration of the aramid fiber polymer dispersion liquid and the working pressure of the compressed gas, the atomized micro-nano aramid polymer molecular chains are disturbed and dispersed by receiving airflow in a turbulent flow zone and are stretched and arranged under the action of an airflow field, and the aramid fiber micro-nanofiber dispersion liquid is obtained after solidification; and then through further ultramicron defibrination treatment, longitudinal separation of aramid fibers is realized, and the controllability and adjustability of the size of the micro-nanofiber are realized.
Description
Technical Field
The invention relates to the technical field of polymer materials, in particular to aramid nano-fibers, a preparation method and application thereof, and a preparation method of aramid paper.
Background
In recent years, high-performance fiber materials have excellent mechanical properties, dielectric strength, chemical and thermal stability, and play an important role in high-tech development fields such as aerospace, transportation, electric power communication, national defense industry and the like, and have become one of the hot spots for new material research in the 21 st century. The nano-scale aramid fiber has the advantages of both high-performance aramid fiber and polymer nanofiber, and can effectively solve the problems of smooth surface and unsatisfactory composite effect of the conventional aramid fiber to a certain extent. However, as an important member of a high-performance aromatic polyester fiber family, the characteristics of high strength, high modulus, high temperature resistance, corrosion resistance and the like of the aramid fiber bring certain difficulties for realizing controllable nano-preparation, which also results in less technologies available for preparing the aramid nanofiber at present.
The currently disclosed preparation methods of the aramid nanofibers comprise electrostatic spinning, rotary jet spinning, alkali-synergistic mechanical milling and hydrolysis, an alkali dissolution method, a polymerization and dispersion method and the like; wherein, the electrostatic spinning method has low production efficiency and difficult size regulation; the alkali fusion method needs to dissolve aramid fiber and then disperse, and is complex in process; the mechanical method has high energy consumption and large power consumption; the existing jet spinning technology adopts an inner liquid inlet pipe and an outer air inlet pipe, and the prepared aramid fiber has the advantages of large diameter, uncontrollable length and wide size distribution range.
The technical defects limit the industrialization process and the application range of the aramid nano-fiber. Therefore, there is a need for an improvement in the existing methods for producing aramid nanofibers.
Disclosure of Invention
In view of the above, the invention provides a preparation method of aramid nanofiber, and a preparation method and application thereof, so as to solve or partially solve the technical problems in the prior art.
In a first aspect, the invention provides a preparation method of aramid nano-fibers, which comprises the following steps:
dispersing an aramid polymer into a first solvent to prepare an aramid polymer dispersion liquid;
spraying the aramid polymer dispersion liquid into a second solvent with a curing effect after air-jet atomization treatment to obtain an aramid micro-nanofiber dispersion liquid;
and then carrying out ultramicro-grain grinding treatment on the aramid fiber micro-nano fiber dispersion liquid to obtain the aramid fiber nano fibers.
Preferably, in the preparation method of the aramid nanofiber, the first solvent comprises one or more of dimethylacetamide, dimethylformamide, dimethyl sulfoxide and acetone; the second solvent comprises one or more of dimethylacetamide, dimethylformamide, dimethyl sulfoxide, acetone, a dimethylacetamide aqueous solution, a dimethylformamide aqueous solution, a dimethylsulfoxide aqueous solution and an acetone aqueous solution.
Preferably, the aramid polymer comprises one or more of poly (m-phenylene isophthalamide), poly (p-phenylene terephthalamide) and polyamide polymer containing a heterocyclic ring structure.
Preferably, in the preparation method of the aramid nanofiber, the specific process of the air-jet atomization treatment is as follows: the aperture of the atomization hole is 0.1-8.0 mm, and the pressure of compressed gas is 0.1-1.0 MPa.
Preferably, the preparation method of the aramid nanofiber comprises the following steps of dispersing the aramid polymer into the first solvent to prepare the aramid polymer dispersion liquid: dispersing the aramid polymer into a first solvent, and stirring for 1-60 min at 50-1000 rpm to obtain an aramid polymer dispersion liquid.
Preferably, the preparation method of the aramid nanofiber comprises the following specific process of ultrafine particle grinding treatment: the gap between the grinding discs is-100 mu m to 100 mu m, and the grinding times is 1 to 100.
Preferably, in the preparation method of the aramid nanofiber, the mass concentration of the aramid polymer dispersion liquid is 0.01-20%.
Preferably, in the method for preparing the aramid nanofibers, the mass concentrations of the dimethylacetamide aqueous solution, the dimethylformamide aqueous solution, the dimethyl sulfoxide aqueous solution and the acetone aqueous solution are all 0-60%.
In a second aspect, the invention also provides aramid nano-fibers prepared by the preparation method.
In a third aspect, the invention also provides application of the aramid nano-fiber in preparation of composite reinforced materials, battery diaphragms, electric insulation nano-paper, flexible electronic devices and adsorption filter media.
In a third aspect, the invention also provides a preparation method of the aramid paper, which is characterized by comprising the following steps:
mixing the aramid nano-fiber, the aramid chopped fiber and the aramid pulp to obtain a fiber dispersion liquid;
defibering the fiber dispersion liquid, making sheets by a Kaiser method to prepare base paper, and carrying out hot pressing to obtain the aramid paper.
The aramid nanofiber and the preparation method and application thereof in the prior art have the following beneficial effects:
(1) According to the preparation method of the aramid nano-fiber, the aramid polymer dispersion liquid is disordered and dispersed by using high-speed flowing compressed gas, the atomized aramid polymer dispersion liquid is fully mixed with the second solvent with a solidification effect to obtain the aramid micro-nanofiber dispersion liquid, the aramid polymer arrangement structure can be regulated and controlled by adjusting the concentration of the aramid polymer dispersion liquid and the working pressure of the compressed gas, the atomized micro-nano aramid polymer molecular chains are subjected to airflow disturbance and dispersion in a turbulent flow zone and are stretched and arranged under the action of an airflow field, and the aramid micro-nanofiber dispersion liquid is obtained after solidification; then, longitudinal separation of aramid fibers is realized through further ultrafine grain grinding treatment, and the size of the micro-nano fibers is controllable and adjustable;
(2) According to the preparation method of the aramid nanofiber, the prepared micro-nanofiber has a unique fibrillating structure and a larger specific surface area, the bonding strength of the fiber interface in the aramid paper can be obviously improved, the mechanical strength and the dielectric property of the aramid paper can be effectively improved, and the method can be widely applied to the field of new high-end insulating materials.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the embodiments or the prior art descriptions will be briefly described below. It is obvious that the drawings in the following description are only some embodiments of the invention, and that for a person skilled in the art, other drawings can be derived from them without inventive effort.
Fig. 1 is a schematic flow diagram of a preparation method of aramid nanofibers according to the present invention;
FIG. 2 is an SEM image of the surface morphology of the aramid nanofibers prepared in example 4 of the present invention;
fig. 3 is a diameter frequency histogram of the aramid nanofibers prepared in example 4 of the present invention.
Detailed Description
In the following, the technical solutions in the embodiments of the present invention will be clearly and completely described in conjunction with the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be obtained by a person skilled in the art without making any creative effort based on the embodiments of the present invention, belong to the protection scope of the present invention.
The embodiment of the application provides a preparation method of aramid nanofibers, as shown in fig. 1, comprising the following steps:
s1, dispersing an aramid polymer into a first solvent to prepare an aramid polymer dispersion liquid;
s2, spraying the aramid polymer dispersion liquid into a second solvent with a curing effect after air-jet atomization treatment to obtain an aramid micro-nanofiber dispersion liquid;
and S3, carrying out ultramicro-grinding treatment on the aramid fiber micro-nano fiber dispersion liquid to obtain the aramid fiber nano fibers.
The preparation method of the aramid nanofiber has the following principle of air-jet atomization treatment: by utilizing a compression type atomizer (also called a jet atomizer), according to a Venturi injection principle, high-speed airflow is formed by utilizing compressed gas through a fine pipe orifice, the generated negative pressure drives aramid polymer dispersion liquid to be injected onto an obstacle together, and the aramid polymer dispersion liquid splashes around under high-speed impact to change liquid drops into vaporous particles to be injected out of an atomizing hole; the aramid fiber micro-nano fiber dispersion liquid is disordered and dispersed by using high-speed flowing compressed gas, the atomized aramid fiber polymer dispersion liquid is fully mixed with a second solvent with a solidification effect to obtain the aramid fiber micro-nano fiber dispersion liquid, the aramid fiber polymer arrangement structure can be regulated and controlled by adjusting the concentration of the aramid fiber polymer dispersion liquid and the working pressure of the compressed gas, the atomized micro-nano aramid fiber polymer molecular chains are disturbed and dispersed by airflow in a turbulent flow zone and are stretched and arranged under the action of an airflow field, and the aramid fiber micro-nano fiber dispersion liquid is obtained after solidification; and then, longitudinal separation of aramid fibers is realized through further optimized ultramicron pulping treatment, and the size of the micro-nanofiber is controllable and adjustable. The micro-nanofiber prepared by the preparation method of the aramid nanofiber has a unique fibrillating structure and a larger specific surface area, can obviously improve the bonding strength of a fiber interface in aramid paper, effectively improves the mechanical strength and the dielectric property of the aramid paper, and can be widely applied to the field of new high-end insulating materials. The preparation method of the aramid nano-fiber is simple in preparation operation, convenient and easy to implement, high in production efficiency compared with the conventional preparation method at present, and suitable for industrial continuous production. The preparation method of the aramid nano-fiber can also add functional groups into the aramid polymer to increase the functionalization and high performance of the aramid polymer, and has important significance for the cross diversified application of the aramid nano-fiber in various fields such as reinforced materials, battery diaphragms, electric insulation nano-paper, flexible electronic devices, adsorption and filtration media and the like.
In some embodiments, the first solvent comprises one or more of dimethylacetamide, dimethylformamide, dimethylsulfoxide, acetone;
the second solvent comprises one or more of dimethylacetamide, dimethylformamide, dimethyl sulfoxide, acetone, an aqueous solution of dimethylacetamide, an aqueous solution of dimethylformamide, an aqueous solution of dimethyl sulfoxide and an aqueous solution of acetone.
In the above embodiments, the second solvent may be other solvents that can be cured with the aramid polymer dispersion liquid, besides dimethylacetamide, dimethylformamide, dimethylsulfoxide, acetone, dimethylacetamide, and the like, and their corresponding aqueous solutions.
In some embodiments, the aramid polymer includes one or more of poly (m-phenylene isophthalamide), poly (p-phenylene terephthalamide), and polyamide polymers containing heterocyclic structures. Specifically, poly (m-phenylene isophthalamide) (PMIA) is a polymer prepared by polycondensation of m-phenylene diamine and isophthaloyl dichloride, and is also called aramid 1313; poly (p-phenylene terephthalamide) (PPTA) is a fully para-polyaramid prepared by condensation polymerization of p-phenylene diamine and paraphthaloyl chloride, also known as aramid 1414. As the polyamide polymer having a heterocyclic structure in the examples of the present application, piperazine aromatic polyamide, piperazine aromatic nylon, and polyquine can be used
And (3) a quinoline dione amide.
In some embodiments, the specific process of the gas-spray atomization treatment is: the aperture of the atomization hole is 0.1-8.0 mm, and the pressure of compressed gas is 0.1-1.0 MPa. The compressed atomizer adopted in the gas spraying atomization treatment in the embodiment of the application is the conventional compressed atomizer, the aperture of an atomization hole is 0.1-8.0 mm, the working pressure of compressed gas during atomization is 0.1-1.0 MPa, and the adopted compressed gas comprises one or more of air, nitrogen and argon.
In some embodiments, the preparation of the aramid polymer dispersion by dispersing the aramid polymer into the first solvent is specifically: dispersing the aramid polymer into a first solvent, and stirring for 1-60 min at 50-1000 rpm to obtain an aramid polymer dispersion liquid.
In some embodiments, the specific process of the superfine particle grinding treatment is as follows: the gap between the grinding discs is-100 mu m to 100 mu m, and the grinding times is 1 to 100. In the examples of the present application, the ultrafine grain grinding treatment was carried out by using an existing ultrafine grain refiner.
In some embodiments, the aramid polymer dispersion liquid is sprayed into the second solvent after being subjected to air-jet atomization treatment, and then is stirred at 50-1000 rpm for 1-60 min to obtain the aramid micro-nanofiber dispersion liquid.
In some embodiments, the mass concentration of the aramid polymer dispersion is 0.01 to 20%.
In some embodiments, the mass concentration of the aqueous dimethylacetamide solution, the aqueous dimethylformamide solution, the aqueous dimethylsulfoxide solution and the aqueous acetone solution is 0 to 60%. In the examples of the present application, the mass concentration of the aqueous solution of dimethylacetamide or the like means the mass fraction of dimethylacetamide or the like in the whole solution, and the mass concentration is 0, means that the second solvent used is water.
Based on the same inventive concept, the embodiment of the application also provides the aramid nano-fiber prepared by the preparation method. The aramid nano-fiber prepared by the method is in a highly fibrillated hairiness shape, and the average diameter is less than 100nm.
Based on the same inventive concept, the embodiment of the application also provides application of the aramid nanofiber in preparation of composite reinforced materials, battery diaphragms, electric insulation nano paper, flexible electronic devices and adsorption filter media.
Based on the same inventive concept, the embodiment of the present application further provides a method comprising the following steps:
mixing the prepared aramid nano-fiber, aramid chopped fiber and aramid pulp to obtain a fiber dispersion liquid;
defibering the fiber dispersion liquid, making sheets by a Kaiser method to prepare base paper, and carrying out hot pressing to obtain the aramid paper.
Specifically, the aramid chopped fibers used in the present application may be meta-polyamide fibers (aramid 1313) and para-polyamide fibers (aramid 1414); the mass ratio of the aramid nano-fiber to the aramid chopped fiber to the aramid pulp is 1 (4-5) to 4-5; the fluffing is carried out by a fluffer for fluffing 15000-25000 r; the hot pressing process specifically comprises the following steps: hot pressing at 180-220 deg.c and 3-6 MPa for 1-2 min; before defibering, the fiber dispersion is diluted by water to the mass concentration of 0.1-0.3%.
The following further describes, in a specific example, a method for producing the aramid nanofibers and the aramid paper of the present invention.
Example 1
The embodiment of the application provides a preparation method of aramid nano-fiber, which comprises the following steps:
s1, dispersing polyisophthaloyl metaphenylene diamine in a dimethylacetamide solvent at room temperature, and stirring for 10min at a rotating speed of 500rpm to obtain an aramid polymer dispersion liquid with a mass fraction of 10%;
s2, spraying the aramid polymer dispersion liquid obtained in the step S1 into water after air spray atomization treatment, and stirring at the rotating speed of 500rpm for 60min to obtain an aramid micro-nanofiber dispersion liquid;
s3, carrying out ultramicro-grinding treatment on the aramid fiber micro-nano fiber dispersion liquid to obtain aramid fiber nano fibers;
wherein, the gas-spray atomization treatment process comprises the following steps: the aperture of the atomization hole is 0.1mm, the working pressure of compressed gas during atomization is 0.1MPa, and the adopted compressed gas is air;
the specific process of the superfine particle grinding treatment comprises the following steps: the gap between the grinding discs is 100 μm, and the grinding times are 100 times.
Example 2
The embodiment of the application provides a preparation method of aramid nano-fiber, which comprises the following steps:
s1, dispersing polyisophthaloyl metaphenylene diamine in a dimethylacetamide solvent at room temperature, and stirring for 10min at a rotating speed of 500rpm to obtain an aramid polymer dispersion liquid with a mass fraction of 10%;
s2, spraying the aramid polymer dispersion liquid obtained in the S1 into a dimethylacetamide aqueous solution after air spray atomization treatment, and stirring at the rotating speed of 1000rpm for 20min to obtain an aramid micro-nanofiber dispersion liquid;
s3, carrying out ultramicro-grinding treatment on the aramid fiber micro-nano fiber dispersion liquid to obtain aramid fiber nano fibers;
wherein, the gas-spray atomization treatment process comprises the following steps: the aperture of the atomization hole is 2mm, the working pressure of compressed gas during atomization is 0.6MPa, and the adopted compressed gas is air;
the specific process of the superfine particle grinding treatment comprises the following steps: the gap between the millstones is 10 mu m, and the grinding times are 10 times; the mass concentration of the dimethylacetamide aqueous solution was 50%.
Example 3
The embodiment of the application provides a preparation method of aramid nano-fiber, which comprises the following steps:
s1, dispersing polyisophthaloyl metaphenylene diamine in a dimethylacetamide solvent at room temperature, and stirring for 20min at a rotating speed of 500rpm to obtain an aramid polymer dispersion liquid with the mass fraction of 20%;
s2, spraying the aramid polymer dispersion liquid obtained in the S1 into a dimethylacetamide aqueous solution after air spray atomization treatment, and stirring for 60min at the rotating speed of 500rpm to obtain an aramid micro-nanofiber dispersion liquid;
s3, carrying out ultramicro-grinding treatment on the aramid fiber micro-nano fiber dispersion liquid to obtain aramid fiber nano fibers;
wherein, the gas-spray atomization treatment process comprises the following steps: the aperture of the atomization hole is 8mm, the working pressure of compressed gas during atomization is 1.0MPa, and the adopted compressed gas is air;
the specific process of the ultrafine particle grinding treatment comprises the following steps: the gap between the millstones is-20 mu m, and the grinding times are 10 times; the mass concentration of the dimethylacetamide aqueous solution is 60%.
Example 4
The embodiment of the application provides a preparation method of aramid nano-fibers, which comprises the following steps:
s1, dispersing polyisophthaloyl metaphenylene diamine in a dimethylacetamide solvent at room temperature, and stirring at the rotating speed of 1000rpm for 1min to obtain an aramid polymer dispersion liquid with the mass fraction of 12%;
s2, spraying the aramid polymer dispersion liquid obtained in the S1 into a dimethylacetamide aqueous solution after air spray atomization treatment, and stirring for 60min at the rotating speed of 100rpm to obtain an aramid micro-nanofiber dispersion liquid;
s3, performing ultramicro-grain pulping treatment on the aramid micro-nanofiber dispersion liquid to obtain aramid nanofibers;
wherein, the gas-spray atomization treatment process comprises the following steps: the aperture of the atomization hole is 5mm, the working pressure of compressed gas during atomization is 0.7MPa, and the adopted compressed gas is air;
the specific process of the superfine particle grinding treatment comprises the following steps: the gap between the millstones is-100 mu m, and the grinding times are 20 times; the mass concentration of the dimethylacetamide aqueous solution is 60%.
Performance testing
The surface topography SEM image of the aramid nanofibers prepared in example 4 is shown in fig. 2. As can be seen from figure 2, the aramid nanofiber prepared by the method is in a hairiness shape and has a unique high-degree fibrillating structure.
The diameter frequency histogram of the aramid nanofibers prepared in example 4 is shown in fig. 3.
The results of testing the average diameter and the specific surface area of the aramid nanofibers prepared in examples 1 to 4 are shown in table 1 below.
Table 1-mean diameter and specific surface area of the aramid nanofibers prepared in different examples
| Examples | Average diameter (nm) | Specific surface area (m) 2 /g) |
| Example 1 | 112.7 | 194.6 |
| Example 2 | 72.7 | 274.3 |
| Example 3 | 52.4 | 369.1 |
| Example 4 | 28.9 | 558.2 |
As can be seen from Table 1, the aramid nanofibers prepared in examples 1 to 4 of the present application have an average diameter of 28.9 to 112.7nm and a specific surface area of 194.6 to 558.2m 2 The size distribution range of the aramid nano-fiber is wide, and the size of the aramid nano-fiber can be controlled and adjusted by adjusting the concentration of the aramid polymer dispersion liquid, different air-jet atomization treatment processes and ultrafine particle grinding treatment.
Example 5
The embodiment of the application provides a preparation method of aramid paper, which comprises the following steps:
mixing the aramid nano-fiber, the meta-aramid chopped fiber and the aramid pulp prepared in the embodiment 1 to obtain a fiber dispersion liquid;
diluting the fiber dispersion liquid with water to a mass concentration of 0.1%;
defibering the diluted fiber dispersion liquid with a defibering machine at 20000r, and making into sheet with Kaiser method to obtain the final product with a quantitative of 40g/m 2 Carrying out hot pressing on the base paper at 200 ℃ and 5MPa for 1min to obtain aramid paper;
the mass ratio of the aramid nano-fiber to the aramid chopped fiber to the aramid pulp is 1.5.
Example 6
The embodiment of the application provides a preparation method of aramid paper, which is the same as embodiment 5 except that the used aramid nanofibers are the aramid nanofibers prepared in embodiment 2.
Example 7
The embodiment of the application provides a preparation method of aramid paper, which is the same as the embodiment 5 except that the used aramid nanofibers are the aramid nanofibers prepared in the embodiment 3.
Example 8
The embodiment of the application provides a preparation method of aramid paper, which is the same as embodiment 5 except that the used aramid nanofibers are the aramid nanofibers prepared in embodiment 4.
Comparative example 1
The comparative example provides a preparation method of aramid paper, which comprises the following steps:
mixing the meta-aramid chopped fibers and the aramid pulp to obtain a fiber dispersion liquid;
diluting the fiber dispersion liquid with water to a mass concentration of 0.1%;
defibering the diluted fiber dispersion with a defibering machine 20000r, and making into sheet with Kaiser method to obtain a quantitative of 40g/m 2 Carrying out hot pressing on the base paper at 200 ℃ and 5MPa for 1min to obtain aramid paper;
wherein the mass ratio of the aramid chopped fibers to the aramid pulp is 5.
The aramid papers prepared in examples 5 to 8 and comparative example 1 were tested for tensile strength, tear strength, electrical strength, and dielectric constant, and the results are shown in table 2 below.
The performance detection standard of the aramid paper provided by the embodiment of the invention is as follows:
testing the tensile strength of the aramid paper by GB/T453-2002; the tearing strength is tested by GB/T455-2002; the electrical strength is tested by GB/T1408.1-2016; the dielectric constant was tested using GB/T1409-2006.
Testing the thermal shrinkage rate: the paper pattern was cut into 40X 40mm paper patterns, treated in an oven at 300 ℃ for 1 hour, and the heat shrinkage was calculated from the measured change in length according to the following formula: r = (1-L/L) 0 )*100％
R is thermal shrinkage, L is the side length of the square after heat treatment, L 0 Is the original square side length.
Table 2-properties of aramid papers prepared in different examples
As can be seen from Table 2, the aramid nanofiber prepared by the invention has obvious application effect and wide application prospect in the field of high-strength high-temperature-resistant aramid paper.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and should not be taken as limiting the scope of the present invention, which is intended to cover any modifications, equivalents, improvements, etc. within the spirit and scope of the present invention.
Claims (7)
1. The preparation method of the aramid nanofiber is characterized by comprising the following steps of:
dispersing an aramid polymer into a first solvent to prepare an aramid polymer dispersion liquid;
spraying the aramid polymer dispersion liquid into a second solvent with a curing effect after air-jet atomization treatment to obtain an aramid micro-nanofiber dispersion liquid;
then carrying out ultramicro grinding treatment on the aramid fiber micro-nano fiber dispersion liquid to obtain aramid fiber nano fibers;
the specific process of the superfine particle grinding treatment comprises the following steps: the gap between the millstones is-100 mu m to 100 mu m, and the grinding times is 1 to 100;
the mass concentration of the aramid polymer dispersion liquid is 0.01-20%;
the first solvent comprises one or more of dimethylacetamide, dimethylformamide, dimethyl sulfoxide and acetone; the second solvent comprises one or more of dimethylacetamide, dimethylformamide, dimethyl sulfoxide, acetone, a dimethylacetamide aqueous solution, a dimethylformamide aqueous solution, a dimethylsulfoxide aqueous solution and an acetone aqueous solution;
the mass concentrations of the dimethylacetamide aqueous solution, the dimethylformamide aqueous solution, the dimethyl sulfoxide aqueous solution and the acetone aqueous solution are all 0-60%.
2. The method for preparing the aramid nanofiber as claimed in claim 1, wherein the aramid polymer comprises one or more of poly (m-phenylene isophthalamide), poly (p-phenylene terephthalamide), and polyamide polymer containing a heterocyclic structure.
3. The preparation method of the aramid nanofiber as claimed in claim 1, wherein the specific process of the air-jet atomization treatment is as follows: the aperture of the atomization hole is 0.1-8.0 mm, and the pressure of compressed gas is 0.1-1.0 MPa.
4. The preparation method of the aramid nanofiber as claimed in claim 1, wherein the preparation of the aramid polymer dispersion by dispersing the aramid polymer into the first solvent is specifically: dispersing the aramid polymer into a first solvent, and stirring for 1-60 min at 50-1000 rpm to obtain an aramid polymer dispersion liquid.
5. An aramid nanofiber characterized by being prepared by the preparation method of any one of claims 1 to 4.
6. Use of the aramid nanofibers according to claim 5 in the preparation of composite reinforcement materials, battery separators, electrically insulating nanopapers, flexible electronic devices, adsorption filtration media.
7. The preparation method of the aramid paper is characterized by comprising the following steps of:
mixing the aramid nanofibers, the aramid chopped fibers and the aramid pulp of claim 6 to obtain a fiber dispersion liquid;
defibering the fiber dispersion liquid, making sheets by a Kaiser method to prepare base paper, and carrying out hot pressing to obtain the aramid paper.
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5874029A (en) * | 1996-10-09 | 1999-02-23 | The University Of Kansas | Methods for particle micronization and nanonization by recrystallization from organic solutions sprayed into a compressed antisolvent |
| CN103835133A (en) * | 2014-03-18 | 2014-06-04 | 浙江理工大学 | Method for preparing fluorine-free super-hydrophobic textile surface |
| CN103846784A (en) * | 2012-11-30 | 2014-06-11 | 大连金成盛世重工有限公司 | Grinding disc |
| CN106512873A (en) * | 2015-09-09 | 2017-03-22 | 中国科学院理化技术研究所 | Method for encapsulating large quantity of nano particles and obtained micro nano composite microsphere and application of micro nano composite microsphere |
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| BRPI0903844B1 (en) * | 2009-06-15 | 2021-03-02 | Empresa Brasileira De Pesquisa Agropecuária - Embrapa | method and apparatus for producing micro and / or nanofiber blankets from polymers |
| WO2015016450A1 (en) * | 2013-08-01 | 2015-02-05 | (주)에프티이앤이 | Multi-layered nanofiber filter medium using electro-blowing, melt-blowing or electrospinning, and method for manufacturing same |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5874029A (en) * | 1996-10-09 | 1999-02-23 | The University Of Kansas | Methods for particle micronization and nanonization by recrystallization from organic solutions sprayed into a compressed antisolvent |
| CN103846784A (en) * | 2012-11-30 | 2014-06-11 | 大连金成盛世重工有限公司 | Grinding disc |
| CN103835133A (en) * | 2014-03-18 | 2014-06-04 | 浙江理工大学 | Method for preparing fluorine-free super-hydrophobic textile surface |
| CN106512873A (en) * | 2015-09-09 | 2017-03-22 | 中国科学院理化技术研究所 | Method for encapsulating large quantity of nano particles and obtained micro nano composite microsphere and application of micro nano composite microsphere |
Non-Patent Citations (1)
| Title |
|---|
| 喷雾干燥法制备水分散聚酰亚胺;井晶等;《高等学校化学学报》;20091010(第10期);第2086-2087页1.2实验过程 * |
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