CN111925547A - Polyethylene film with fluorine-containing polymer composite coating and preparation method thereof - Google Patents

Polyethylene film with fluorine-containing polymer composite coating and preparation method thereof Download PDF

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Publication number
CN111925547A
CN111925547A CN202011108449.1A CN202011108449A CN111925547A CN 111925547 A CN111925547 A CN 111925547A CN 202011108449 A CN202011108449 A CN 202011108449A CN 111925547 A CN111925547 A CN 111925547A
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film
coating
wiping
roller
area
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CN111925547B (en
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闫银凤
周宏涛
杨连新
杨武涛
朱亚凯
郝自娟
阮德谦
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Henan Functional Polymer Membrane Material Innovation Center Co ltd
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Henan Functional Polymer Membrane Material Innovation Center Co ltd
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    • 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
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/042Coating with two or more layers, where at least one layer of a composition contains a polymer binder
    • C08J7/0423Coating with two or more layers, where at least one layer of a composition contains a polymer binder with at least one layer of inorganic material and at least one layer of a composition containing a polymer binder
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/02Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber
    • B05D7/04Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber to surfaces of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/24Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials for applying particular liquids or other fluent materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C55/00Shaping by stretching, e.g. drawing through a die; Apparatus therefor
    • B29C55/02Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
    • B29C55/10Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial
    • B29C55/12Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial biaxial
    • 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
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • 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
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/06Coating with compositions not containing macromolecular substances
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D127/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C09D127/16Homopolymers or copolymers of vinylidene fluoride
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2506/00Halogenated polymers
    • B05D2506/10Fluorinated polymers
    • 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
    • C08J2391/00Characterised by the use of oils, fats or waxes; Derivatives thereof
    • C08J2391/06Waxes
    • 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
    • C08J2423/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2423/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2423/04Homopolymers or copolymers of ethene
    • C08J2423/06Polyethene
    • 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
    • C08J2427/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2427/02Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2427/12Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08J2427/16Homopolymers or copolymers of vinylidene fluoride
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/37Thiols
    • C08K5/375Thiols containing six-membered aromatic rings
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

A preparation method of a polyethylene film with a fluorine-containing polymer composite coating comprises the steps of preparing a polyethylene film; performing two-dimensional stretching after conventional stretching; and coating a first layer of coating on the film, sputtering a second layer of coating on the film, and forming the film after coating falling inspection and feedback treatment. The film thus produced has high safety, excellent mechanical and electrical properties.

Description

Polyethylene film with fluorine-containing polymer composite coating and preparation method thereof
Technical Field
The invention relates to the technical field of lithium battery diaphragms and preparation thereof.
Background
The diaphragm is an important component in the lithium battery, and directly determines the service performance and safety of the lithium battery. Typically the separator is an insulating material having a porous structure. Lithium dendrite is inevitably generated during the use of the lithium battery, and it continuously grows and pierces the separator, thereby causing a safety accident. In the prior art, a ceramic coating is used to prevent lithium dendrite from growing and puncturing a diaphragm, but the reaction of Si element in the ceramic and metallic lithium causes excessive loss of effective lithium in the battery, thereby affecting the electrical performance of the lithium battery.
In addition, the protection of the coating on the diaphragm is more theoretically realized, and the falling fragments of the coating can pierce the film during actual use to directly cause safety hazards. In addition, the uneven thin film coating caused by the falling of the coating can also cause the local burden of the diaphragm to be intensified under the working condition environment with large current and high temperature, thereby greatly causing the deterioration of electrical performance and the hidden danger of safety.
Typical coating tests are destructive, taking a portion of the film as a sample. This method is not suitable for production line, and can not perform feedback control on the production process in real time, but only be used for subsequent quality inspection. And the existing inspection uses special friction blocks, which are not exactly the same as the friction actually encountered by the film. The friction is dry grinding, which restores the partial scene of the film coating falling off, but the film is mostly in a dry environment during production, transportation, storage and installation, but needs to be in contact with electrolyte during actual use, and is in a wet environment, and the condition of the coating falling off is greatly different. In conclusion, the prior art can not accurately simulate the real situation.
Therefore, a preparation process which can accurately simulate real conditions and is directly applied to a production line is urgently needed, and the preparation process can increase the firmness of a lithium battery diaphragm coating, avoid mechanical falling and chemical reaction, enhance the electrical performance of a lithium battery diaphragm and reduce potential safety hazards.
Disclosure of Invention
In view of the above problems, the present invention has been made to provide a lithium battery separator and a method for preparing the same, which overcome or at least partially solve the above problems.
A method for preparing a polyethylene film with a fluorine-containing polymer composite coating,
the raw material A is polyethylene and comprises the following two parts
A1: molecular weight 6.5X 106-8.5×106The polyethylene particles of (a);
a2: the density is 0.966-0.983g/cm3The polyethylene particles of (a);
the raw material B is paraffin oil; the raw material D is 4, 4' -thiobis (6-tert-butyl-m-cresol);
step 1: heating and mixing the raw materials in batches; injecting the mixed slurry into an extruder to extrude into a thick film;
step 2: sequentially carrying out longitudinal stretching and transverse stretching on the thick film;
and step 3: the film is transmitted to a two-dimensional stretching device, light transmittance abnormal points on the film are obtained, a stretching area is determined according to the distribution of the abnormal points, and a film two-dimensional stretching process is carried out;
and 4, step 4: performing first layer coating on the film: mixing 4.4 parts by mass of deionized water, 1 part by mass of polyvinylidene fluoride, 0.15 part by mass of sodium polyacrylate and 1.3 parts by mass of silicon dioxide powder, and performing ball milling to obtain coating slurry; coating the prepared coating slurry on one side of the diaphragm; then, drying step by step to finally obtain a film with a first coating;
and 5: and (3) sputtering a second coating layer on the film: putting the film with the first coating into a drying box for fully drying; after drying, sputtering aluminum particles on the surface of the film by a magnetron sputtering method, and forming a second coating on the surface of the first coating after sputtering;
step 6: the film with two layers of coatings was subjected to the following treatment process:
(1) curling treatment: feeding the film into a plurality of curling rollers which are arranged in a vertical crossed way, and repeatedly curling the film;
(2) dry wiping treatment: during the curling process, the dry wiping roller transmits the dry wiping material to the curling part above the curling roller, and when the area to be wiped is transmitted to the roller, the dry wiping roller moves downwards quickly, so that the dry wiping material is separated after rapidly contacting the area to be wiped of the film, the dry wiping of the surface of the film is realized, and a dry wiping area is formed;
(3) wet wiping treatment: during the curling treatment, the wet wiping roller transmits wet wiping materials to the curling part above the curling roller, and when the area to be wiped is transmitted to the roller, the wet wiping roller moves downwards quickly, so that the wet wiping materials are separated after rapidly contacting the area to be wiped of the film, the wet wiping on the surface of the film is realized, and a wet wiping area is formed;
(4) heating treatment: when the curling treatment, the dry wiping treatment and the wet wiping treatment are carried out, a temperature control device is utilized to control the environment temperature to respectively reach the starting temperature, the normal working temperature and the limit working temperature of the conventional lithium battery;
and 7: the coating was examined and analyzed:
(1) after the dry wiping is finished, shooting an image of the dry wiping material by using a first inspection camera, and comparing the image with a standard image so as to judge the dry wiping stability of the coating of the film;
(2) after wet wiping is finished, shooting an image of the wet wiping material by using a second inspection camera, and comparing the image with a standard image so as to judge the wet wiping stability of the coating of the film;
(3) after the curling treatment, the dry wiping treatment and the wet wiping treatment are finished, a dry wiping area, a wet wiping area and a non-wiping area of the film are irradiated by structured light, corresponding images are shot by a third camera and are compared with standard images of three areas stored in advance, and therefore the comprehensive stability of the film coating is determined;
and (4) integrating dry wiping stability, wet wiping stability and integrated stability to obtain the falling risk condition of the film coating.
Wherein the thickness of the first coating layer is controlled to be 2-3 μm.
Wherein the thickness of the second coating layer is controlled to be 0.5-0.8 μm.
The step-by-step drying comprises drying at 45 deg.C, 50 deg.C, 60 deg.C, and 65 deg.C
A lithium battery diaphragm and a preparation device thereof are prepared by the method.
Invention and technical effects
1. The component structure and the preparation process of the polyethylene film coating are optimized, the lithium battery diaphragm is prevented from being broken under severe working conditions to the maximum extent, and the electrical performance of the lithium battery diaphragm is not influenced.
2. The coating falling simulation inspection process which is more in line with the practical use condition is set, and the coating process is controlled by utilizing the feedback of the detection result, so that the safety and the electrical property of the film finished product are ensured.
3. The dry contact and wet contact type film falling simulation is respectively carried out at different temperatures, so that the actual use working conditions are better met, more accurate detection results can be obtained, the production process can be accurately fed back and controlled, and the quality of finished products is ensured.
Drawings
Various other advantages and benefits will become apparent to those of ordinary skill in the art upon reading the following detailed description of the preferred embodiments. The drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the invention. Also, like reference numerals are used to refer to like parts throughout the drawings. In the drawings:
FIG. 1 is a flow chart of a process for making a separator with a composite coating
FIG. 2 is a top view of a two-dimensional stretching process of a separator
FIG. 3 is a rear view of a two-dimensional stretching process of a separator
FIG. 4 is a front view of a process for stretching a separator in two dimensions
FIG. 5 is a schematic diagram of a two-dimensional stretching process of a separator
FIG. 6 is a schematic view of a diaphragm coating inspection control process
FIG. 7 is a schematic view of a dry erase region and a wet erase region of a diaphragm
Detailed Description
Exemplary embodiments of the present disclosure will be described in more detail below with reference to the accompanying drawings. While exemplary embodiments of the present disclosure are shown in the drawings, it should be understood that the present disclosure may be embodied in various forms and should not be limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the disclosure to those skilled in the art.
Diaphragm preparation method
The feedstock a is polyethylene, and in particular, may comprise the following two fractions, and the preferred weight ratio of the two is 1:1.53, according to a number of experiments.
A1: molecular weight 6.5X 106-8.5×106The polyethylene particles of (a);
a2: the density is 0.966-0.983g/cm3The polyethylene particles of (a);
the raw material B is paraffin oil; the raw material D is 4, 4' -thiobis (6-tert-butyl-m-cresol);
wherein the weight ratio of the raw material A to the raw material B is 27: 43, the weight ratio of the raw material D to the raw material A is 0.7: 100.
step 1: mixing the raw material A1, the raw material D and half of the raw material B by weight, heating to 70-110 ℃, stirring for 25 minutes, and keeping the stirring speed at 340 r/min.
Step 2: adding the raw material A2 and the other half of the raw material B by weight into the stirred material obtained in the step 1, mixing, heating to 90-130 ℃, stirring for 5 minutes, keeping the stirring speed at 340 r/min, and finally obtaining slurry.
And step 3: and injecting the mixed slurry into an extruder for extrusion, and keeping the temperature of the extruder at 170-230 ℃ and the extrusion rate at 1100 g/min.
And 4, step 4: cooling and solidifying the extrudate on a cooling roller to form a thick film with the thickness of 400-2500 mu m, wherein the cooling temperature is 20-70 ℃, and solid-liquid phase separation or liquid-liquid phase separation occurs in the cooling and solidifying process, so that a microporous structure is formed in the extrudate.
And 5: setting the temperature of a preheating roller, a longitudinal stretching roller and a cooling roller to be 90 ℃, 120 ℃ and 20 ℃, and longitudinally stretching the thick film through the preheating roller, the longitudinal stretching roller and the cooling roller in sequence to obtain a thin film with the extension ratio of 6-7;
step 6: setting the temperature of a preheating roller, a transverse stretching roller and a cooling roller to be 100 ℃, 125 ℃ and 90 ℃, and transversely stretching the thick film by the preheating roller, the transverse stretching roller and the cooling roller in sequence to obtain a thin film with the elongation ratio of 6-7;
and 7: and (3) conveying the film into a dichloromethane extraction box for extraction, wherein the temperature in the extraction box is 20-35 ℃, and the extraction time is 4 hours. Drying after extraction;
and 8: the film is conveyed to a two-dimensional stretching device for stretching in both transverse and longitudinal directions, and the stretching temperature is kept at 130-150 ℃. Meanwhile, the light transmittance distribution of the film is monitored in the stretching process, so that the force of the stretching device at different stretching positions is controlled, the light transmittance consistency of the film at different positions is adjusted, and the film with better consistency is finally obtained.
And step 9: and cooling to form the film after the two-dimensional stretching is finished.
Step 10: and carrying out first coating on the film.
(1) Coating paste preparation
Mixing 4.4 parts of deionized water and 1 part of polyvinylidene fluoride, and uniformly stirring at the rotating speed of 100 rpm;
then adding 0.15 part of sodium polyacrylate, mixing, uniformly stirring at the rotating speed of 100rpm, and then ball-milling for 15 minutes at the rotating speed of 500 rpm;
then adding 1.3 parts of silicon dioxide powder, mixing, and uniformly stirring at the temperature of 45-65 ℃ and the rotating speed of 300rpm to prepare a uniform solution;
and performing ball milling for 45 minutes at the rotating speed of 800rpm to obtain coating slurry. The above are all parts by mass.
(2) Coating of
Coating the prepared coating slurry on one side of the diaphragm at a coating speed of 6 m/min; then, four drying devices which are arranged in sequence at 45 ℃, 50 ℃, 60 ℃ and 65 ℃ are respectively used for step-by-step drying. Finally, a film with a first coating layer is obtained, wherein the thickness of the first coating layer is controlled to be 2-3 mu m.
The obtained coating can enhance the mechanical strength of the diaphragm, reduce the thermal shrinkage of the diaphragm and avoid safety accidents caused by the fact that lithium dendrites puncture the film.
Step 11: and sputtering a second coating layer on the film.
Putting the film into a drying oven for full drying, wherein the drying temperature is 60-70 ℃, and the drying time is 6 hours;
and after drying, sputtering the nano aluminum particles by a magnetron sputtering method. Firstly, cleaning an aluminum target material by using acetone, drying by using a drying box, carrying out magnetron sputtering on the surface of a film, and controlling the vacuum degree to be 10-4Pa, target distance of 10cm, sputtering power of 110w, sputtering temperature of 30 ℃, sputtering time of 2-5 minutes, and reaction gas of high-purity argon.
And forming a second coating on the surface of the first coating after the sputtering is finished, wherein the thickness of the second coating is controlled to be 0.5-0.8 mu m.
Therefore, a protective film is formed on the surface of the first coating, so that the silicon dioxide in the first coating is not easy to react with the lithium metal, the lithium is prevented from passing, and the first coating is prevented from falling off due to chemical corrosion.
The diaphragm prepared according to the raw material proportion and the process can timely close the open pore when the temperature of the battery is abnormally increased, and can be kept at a higher temperature without the problem of membrane rupture. Meanwhile, the coating material can be prevented from being chemically corroded by the metal lithium while the lithium dendrite is prevented from puncturing the film.
Two-dimensional stretching process in diaphragm manufacturing
In the stretching process, only the thickness of the film is generally monitored to ensure thickness consistency and thus improve the performance of the film. In practice, a number of parameters of the film affect its performance. For example: porosity, pore size, film density, breathability, etc. These properties are usually measured only after the film has been produced, using a number of different devices, to determine whether the film is acceptable. First, doing so requires more equipment; secondly, the detection is post detection, and the produced inferior products cannot be avoided.
The invention provides the detection of the film parameters in the film stretching process and controls the stretching action at the same time, thereby ensuring that the film with higher quality is stretched. However, if a plurality of devices are used for parameter detection, the devices are abnormally complicated, and it is difficult for the control algorithm to balance a plurality of parameters. However, it has been found that, over many years, the above-mentioned non-uniformities in various parameters are ultimately reflected in non-uniformities in the light transmission of the film. Therefore, in order to rapidly control the stretching device in production practice, the invention proposes to use the light transmittance to perform the control of the film stretching, thereby comprehensively controlling the above parameters and obtaining a higher quality diaphragm. Therefore, this is also one of the points of the present invention, and the process thereof will be set forth in detail below.
The two-dimensional stretching equipment comprises a left moving roller 1, a right moving roller 2, an upper left clamping roller 3-1, a lower left clamping roller 3-2, an upper right clamping roller 4-1, a lower right clamping roller 4-2, a rear side edge clamping part 5-1, a rear side edge lower clamping part 5-2, a front side edge clamping part 6-1, a front side edge lower clamping part 6-2, a rear side edge driving part 5-3, a front side edge driving part 6-3, a camera 7 and a surface light source 9.
The left moving roller 1 and the right moving roller 2 are respectively positioned at two ends of the device and used for transmitting the film M, and are simultaneously used for generating left or right pulling force on the film M positioned on the left moving roller and the right moving roller when the film M is respectively translated leftwards or rightwards, and when the other end of the film M is relatively fixed, the longitudinal stretching of the diaphragm is realized.
The upper left clamping roller 3-1 and the lower left clamping roller 3-2 are arranged oppositely up and down and used for clamping the left side of the film M. Wherein the left lower clamping roller 3-2 is fixedly arranged, and the left upper clamping roller 3-1 can move up and down. The upper left pinch roller 3-1 moves downward when the pinching is required, thereby forming the pinching of the left side edge of the film M with the lower left pinch roller 3-2. The upper left clamping roller 3-1 is a plurality of short rollers which can move up and down independently, and the up-and-down movement distance is accurate and controllable. The lower left pinch roll 3-2 is a long roll.
The upper right clamping roller 4-1 and the lower right clamping roller 4-2 are arranged oppositely up and down and used for clamping the right side of the film M. Wherein the right lower clamping roller 4-2 is fixedly arranged, and the right upper clamping roller 4-1 can move up and down. The upper right pinch roller 4-1 moves downward when the pinching is required, thereby forming the pinching of the right side edge of the film M with the lower right pinch roller 4-2. The upper right pinch roll 4-1 is a single long roll, the distance of which up and down moves is precisely controllable. The lower right pinch roll 4-2 is a long roll.
When the upper left pinch roller 3-1 at different positions moves downward by different distances, different intervals are formed at different positions from the lower left pinch roller 3-2, thereby generating different pinching forces to the film M at the corresponding positions. At this time, if the right moving roller 2 moves rightwards, the film M is driven to move rightwards, and at this time, the clamping forces at different positions on the left side of the film M are different, so that for the driving force fixed by the right moving roller 2, the stretching degrees of the longitudinal strip regions of the film M at different positions in the transverse direction are different, and thus different stretching ratios can be generated for the longitudinal strip regions at different positions. Therefore, by controlling the different pitches formed by the upper left pinch roller 3-1 and the lower left pinch roller 3-2 at different positions, the draw ratio of the corresponding sliver region can be controlled. For more precise control, a denser, greater number of upper left pinch rollers may be provided, typically 10, but for higher control resolution, 20-30 may be provided.
When the upper right pinch roller 4-1 moves downwards to form a pinch on the right side edge of the film M together with the lower right pinch roller 4-2, if the left moving roller 1 moves leftwards, the film M is driven to move leftwards, and the film M is uniformly and longitudinally stretched.
Each back side edge clamping part 5-1 and each back side edge lower clamping part 5-2 are arranged oppositely up and down to form a back side edge clamping part together. A plurality of which are arranged along the rear side of the film M for clamping the rear side of the film M. The front side edge clamping part 6-1 and the front side edge lower clamping part 6-2 are arranged oppositely up and down and are a section of a whole, and the front side edge clamping part and the front side edge lower clamping part jointly form a front side edge clamping part used for clamping the front side edge of the film M. The main bodies of the rear side edge clamping part 5-1, the rear side edge lower clamping part 5-2, the front side edge clamping part 6-1 and the front side edge lower clamping part 6-2 are all made of rubber, and the film is prevented from being damaged during clamping. Meanwhile, the rubber is doped with fine iron particles during molding, thereby enhancing the strength of the rubber on the one hand and simultaneously being used for being attracted by the driving part.
The rear side driving part 5-3 is composed of electromagnets and is positioned at the rear side of the rear side edge clamping part 5-1 and the rear side edge lower clamping part 5-2, and the number of the rear side driving parts 5-3 is also a plurality and respectively corresponds to the rear side edge clamping parts which are arranged. The transverse strip-shaped area is used for attracting the corresponding rear side clamping part after being electrified, so that the transverse strip-shaped area corresponding to the position of the film clamped by the rear side clamping part is stretched. Therefore, by controlling the current magnitude of the different rear side driving portions 5-3, the backward stretching force of the rear side clamping portions corresponding to different positions can be controlled, thereby controlling the stretching ratio of the transverse strip-shaped area corresponding to the film. Of course, the front side holding part should fixedly hold the front side of the film while controlling the rear side driving part 5-3 to stretch.
The front side driving portion 6-3 is composed of electromagnets and is located on the front side of the front side clamping portion 6-1 and the front side of the front side lower clamping portion 6-2, and a plurality of rear side driving portions 6-3 are evenly distributed on the front side of the front side clamping portion and used for attracting the corresponding front side clamping portion after being electrified, so that the film clamped by the front side clamping portion is stretched. Although the front side upper holding part 6-1 and the front side lower holding part 6-2 are both single, the main body thereof is made of rubber, and has a certain flexibility. Therefore, by controlling the current of a certain front side driving portion 6-3, the relatively largest pulling force can be generated at the position of the front side clamping portion directly opposite to the front side driving portion 6-3, and the next largest pulling force can be generated at the position adjacent to the position of the front side clamping portion directly opposite to the front side driving portion 6-3. That is, even if only one of the front side driving portions 6-3 is energized, the entire front side of the film can be stretched, but the position corresponding to the front side driving portion 6-3 is stretched most, and the other positions are successively decreased in accordance with the stretch ratio at a distance therefrom. However, since the entire front-side holding portion is an integral whole along the front side of the film, the variation in the stretch ratio at such different positions is actually very small. Therefore, it is very suitable for the case where the stretching ratio at a certain position needs to be finely adjusted. Therefore, the method does not cause drastic change of consistency with an adjacent area due to control of micro stretching of a certain area, thereby ensuring accuracy and high efficiency of process control, and is also one of the invention points. Of course, in the two-dimensional stretching apparatus, only a fine stretching operation is performed, defects at individual positions are adjusted, and a large stretching ratio operation is not performed.
A surface light source 9 is provided above the film M, and a plurality of surface light sources 9 may be provided since the film may be large. However, if the multi-surface light source combination is carried out, the light intensity of any position of the film is the same. The surface light source 9 is used to provide uniform illumination to the film.
The camera 7 is arranged below the film M, and since the film may be large and the field of view of the camera is limited, a plurality of cameras 7 may be arranged to splice the field of view. The camera 7 is for emitting light transmitted through the film from the light source 9 on the receiving surface, and taking an image of the film.
The image obtained above was sent to a processor for analysis as follows:
(1) each pixel point in the image is positionally mapped to an actual point on the film.
(2) Obtaining the gray value P of each pixel point in the imagei
(3) Determining the mean gray-scale value P of the image0
(4) If Pi-P0|/ P0>Q, then P isiThe corresponding film position point is marked as an abnormal point, wherein Q is a set threshold range, which can be selected according to the level of the film consistency requirement, and usually can be selected from 0.01 to 0.1. In this way, it is possible to locate the singular point very simply and conveniently, and thus it is also one of the points of the invention.
(5) And determining a distribution area of the abnormal points, and selecting a rectangular frame with the smallest area to cover the abnormal points, wherein the rectangular frame is used as an area to be stretched in two dimensions. Individual outliers that are isolated can be discarded from consideration.
(6) And controlling corresponding longitudinal stretching mechanisms (a left moving roller 1, a right moving roller 2, a left upper clamping roller 3-1, a left lower clamping roller 3-2, a right upper clamping roller 4-1 and a right lower clamping roller 4-2) and transverse stretching mechanisms (a rear side edge clamping part 5-1, a rear side edge lower clamping part 5-2, a front side edge clamping part 6-1, a front side edge lower clamping part 6-2, a rear side edge driving part 5-3 and a front side edge driving part 6-3) to perform two-dimensional stretching according to the determined stretching area until the area can not cover the distribution area of the abnormal points by using a rectangular frame.
The control method for longitudinal stretching and transverse stretching comprises the following steps:
firstly, when the stretching areas are uniformly distributed at all positions of the film, the upper right clamping roller 4-1 and the lower right clamping roller 4-2 are controlled to approach to clamp the right side of the film, and the left moving roller 1 moves leftwards.
When the stretching areas are distributed in a longitudinal strip shape, controlling the upper left clamping roller 3-1 at the corresponding position to gradually approach the lower left clamping roller 3-2, and generating the maximum clamping force on the position of the film with the minimum distance; the left upper nip roll 3-1 in the remaining positions is also close to the left lower nip roll 3-2, but at a larger pitch, producing less or even no nip force for that position of the film. And controlling the right moving roller 2 to translate to the right, so that the area corresponding to the maximum clamping force is intensively longitudinally stretched, and the rest area is slightly stretched or even not longitudinally stretched.
Thirdly, when the stretching areas are distributed in a transverse strip shape,
if the abnormal condition in the area is serious, inputting larger current to the rear side driving part 5-3 at the corresponding position so as to generate larger pulling force; and the rear side driving part 5-3 at the other positions inputs smaller current, thereby generating smaller tension or even no tension. Such that the respective regions are laterally stretched and the remaining regions are slightly or not laterally stretched.
If there is only a slight abnormal condition in the area, the difference from the peripheral light transmission condition is small. A large current is inputted to the front side driving part 6-3 of the corresponding position, so that a large pulling force is generated and the area corresponding to the position is laterally stretched. However, since the front side edge holding portion 6-1 and the front side edge lower holding portion 6-2 are single, a transverse tension is generated in other positions in the longitudinal direction of the film. But because the main body of the front side clamping part is made of rubber, the front side clamping part has certain flexibility. Therefore, the transverse tension generated at other positions is not greatly different from the transverse tension generated at the abnormal position. Thereby it is avoided that a certain position is stretched in the transverse direction, resulting in excessive stretching.
Those skilled in the art will appreciate that the above stretching process is best suited for use in conjunction with the preparation of the films proposed by the present invention. This does not mean that the stretching process cannot be used for the manufacture of other films. The conventional lithium battery separator may be manufactured using the above-described stretching process.
Through the raw material proportion and the preparation process, the T1 temperature of the finally obtained film is 100 ℃, the T2 temperature is 220 ℃, and the safety of the battery can be effectively ensured. Meanwhile, the service life of the film is prolonged by 15% under a severe working condition, the film breaking probability is reduced by 24%, and the attenuation speed of the lithium battery is basically kept unchanged.
Coating falling inspection control process
Although the mechanical firmness and the chemical firmness of the film coating are ensured through the process design, the yield can be ensured only through strict tests as a production line. In general, coating detection is destructive, and a part of the film is taken as a sample for detection. This approach is not suitable for use on production lines, but only for subsequent quality checks. And the existing inspection uses special friction blocks, which are not exactly the same as the friction actually encountered by the film. The friction is dry grinding, which restores the partial scene of the film coating falling off, but the film is mostly in a dry environment during production, transportation, storage and installation, but needs to be in contact with electrolyte during actual use, and is in a wet environment, and the condition of the coating falling off is greatly different. In conclusion, the prior art can not accurately simulate the real situation, and therefore the invention provides the following coating falling-off inspection control process.
(1) Crimping process
The film M which has been processed is fed by the left transport roller 8-2 of the peeling inspection device, and the film is subjected to a curl inspection through the film curl processing section, simulating a rolling process in production and storage, to judge the peeling of the film in this case. The film curling process section includes a plurality of curling rollers 8-1 arranged to cross up and down for repeatedly curling the film M. Typically 3 for the upper crimping roll and 2 for the lower crimping roll. Preferably, the diameter of each of the crimping rollers is different in order to simulate different degrees of film bending at different locations when the film is rolled.
(2) Dry rub treatment
The dry wiping device and the wet wiping device were subjected to contact drop simulation simultaneously with the curling process. The dry wiping device comprises a dry wiping roller 8-3-1, the dry wiping roller conveys dry wiping materials 8-3-3 to the position above the curling roller on the curling processing part, when the area to be dry wiped is conveyed to the roller, the dry wiping roller 8-3-1 moves downwards quickly to enable the dry wiping materials 8-3-3 to contact the area to be dry wiped of the film M, and then the dry wiping roller 8-3-1 moves upwards quickly to enable the dry wiping materials 8-3-3 to be separated from the film M quickly. Thus, with the movement of the crimping roller 8-1, the area to be dry-wiped of the film M is separated after being rapidly contacted with the dry-wiped material 8-3-3, so that the dry wiping of the surface of the film M is realized, and the dry wiping range is a narrow strip-shaped area along the transverse direction of the film, which is called a dry wiping area 8-8. Thus, the film can be prevented from being damaged in a large range. The dry-cleaning material can be a conventional friction material and can also be a high polymer material. And may preferably be a polyethylene film.
After the dry wiping is finished, the dry wiping roller 8-3-1 conveys the used area of the dry wiping material to the field range of the inspection camera 8-3-2, the inspection camera is used for shooting the image of the dry wiping material and comparing the image with the standard image collected in advance, so that whether the coating fragments are adhered to the dry wiping material or not and the quantity of the coating fragments are judged, and the dry wiping stability of the coating of the film is judged.
(3) Wet scrubbing process
In addition to the dry rub inspection, a wet rub inspection was also performed at the same time as the curling process. The wet wiping device comprises a wet wiping roller 8-4-1, the wet wiping roller conveys wet wiping materials 8-4-3 to the position above the curling roller on the curling processing part, when the area to be wiped is conveyed to the roller, the wet wiping roller 8-4-1 moves downwards quickly to enable the wet wiping materials 8-4-3 to contact the area to be wiped of the film M, and then the wet wiping roller 8-4-1 moves upwards quickly to enable the wet wiping materials 8-4-3 to be separated from the film M quickly. Thus, with the movement of the curling roller 8-1, the area to be wet-wiped of the film M is quickly separated from the wet wiping material 8-4-3 after contacting, so that the wet wiping of the surface of the film M is realized, and the wet wiping range is a narrow strip-shaped area along the transverse direction of the film, which is called a wet wiping area 8-8. Thus, the film can be prevented from being damaged in a large range. The wet wiping material can be a conventional friction material stained with water or electrolyte, and preferably can be a porous polymer material capable of adsorbing water or electrolyte.
After the wet wiping is finished, the wet wiping roller 8-4-1 transmits the used area of the wet wiping material to the field of view of the inspection camera 8-4-2, the inspection camera is used for shooting the image of the wet wiping material, and the image is compared with the standard image collected in advance, so that whether the coating fragments are adhered to the wet wiping material or not and the quantity of the coating fragments are judged, and the wet wiping stability of the coating of the film is judged.
(4) High temperature treatment
In order to simulate more realistically the possible coating detachment of the membrane during the use of the cell. Preferably, the temperature control device 8-7 is used for controlling the ambient temperature when the curling process, the dry wiping process and the wet wiping process are performed. And controlling the environmental temperature to respectively reach the starting temperature, the normal working temperature and the limit working temperature of the conventional lithium battery. At these three temperatures, the curling treatment, the dry wiping treatment and the wet wiping treatment were performed, respectively.
(5) Exfoliation analysis
Shedding analysis was divided into three parts:
firstly, in dry wiping inspection, a dry wiping area inspection camera 8-3-2 inspects coating fragments adsorbed on a dry wiping material. The foregoing has been detailed and will not be repeated.
Secondly, when the wet wiping is detected, the wet wiping area detection camera 8-4-2 detects the coating fragments adsorbed on the wet wiping material. The foregoing has been detailed and will not be repeated.
And thirdly, after the curling treatment, the dry wiping treatment and the wet wiping treatment are finished, the transmission roller 8-2 transmits the film to the inspection area. The inspection area is provided with a laser light source 8-5, a structured light generating device 8-7, and an inspection camera 8-6.
When the dry-wiping area and the wet-wiping area of the film enter the structured light irradiation range, images of the dry-wiping area and the wet-wiping area of the film are collected by the camera 8-6 and are compared with the pre-stored images of the standard dry-wiping area and the standard wet-wiping area, so that the dry-wiping falling-off condition and the wet-wiping falling-off condition of the film are determined. The invention can obtain more accurate detection result by using the structured light. If a uniform light source is used, the intensity variation due to coating fallout is not significant and the spatial resolution is low.
When the non-dry-erasing area and the wet-erasing area (called as non-erasing areas) of the film enter the structured light irradiation range, the image of the non-erasing area of the film is collected by the camera 8-6 and is compared with the pre-stored image of the standard non-erasing area, so that the comprehensive stability of the film coating is determined.
And finally, integrating the contents of the three parts to obtain a film coating falling risk analysis conclusion. And the reverse control of the preparation process is carried out according to the analysis conclusion, and the film coating finally meets the requirements by adjusting the preparation process steps, so that the finished product quality is excellent, and the yield is improved. For example, the composition, heating time, and stretching ratio of the film and/or coating material can be adjusted.
Through the process, the falling probability of the finished coating is reduced by 23.4%, and the safety and the electrical property of the diaphragm are effectively improved.
It is understood that the coating inspection process is used in conjunction with the thin film and coating preparation process of the present invention, but may also be used in other production lines for preparing coated lithium battery thin films.
Although the dry wiping and the wet wiping may cause some damage to a part of the film, the dry wiping and the wet wiping are both separated after being rapidly contacted, so that only a narrow dry wiping/wet wiping area along the width direction is left on the film. This area can then be used for the cutting area of the film. That is, the dry-erase, wet-erase regions may be controlled so as to be located right at the cut portions of the film. Thus, the normal use of the film is not affected.
Those skilled in the art will appreciate that while some embodiments herein include some features included in other embodiments, rather than others, combinations of features of different embodiments are meant to be within the scope of the invention and form different embodiments. For example, in the claims, any of the claimed embodiments may be used in any combination.
Thus, it should be appreciated by those skilled in the art that while a number of exemplary embodiments of the invention have been illustrated and described in detail herein, many other variations or modifications consistent with the principles of the invention may be directly determined or derived from the disclosure of the present invention without departing from the spirit and scope of the invention. Accordingly, the scope of the invention should be understood and interpreted to cover all such other variations or modifications.

Claims (5)

1. A preparation method of a polyethylene film with a fluorine-containing polymer composite coating is characterized by comprising the following steps:
step 1: heating and mixing polyethylene particles, paraffin oil and 4, 4' -thiobis (6-tert-butyl-m-cresol); injecting the mixed slurry into an extruder to extrude into a thick film;
step 2: sequentially carrying out longitudinal stretching and transverse stretching on the thick film;
and step 3: the film is transmitted to a two-dimensional stretching device, light transmittance abnormal points on the film are obtained, a stretching area is determined according to the distribution of the abnormal points, and a film two-dimensional stretching process is carried out;
and 4, step 4: performing first layer coating on the film: mixing 4.4 parts by mass of deionized water, 1 part by mass of polyvinylidene fluoride, 0.15 part by mass of sodium polyacrylate and 1.3 parts by mass of silicon dioxide powder, and performing ball milling to obtain coating slurry; coating the prepared coating slurry on one side of the diaphragm; then, drying step by step to finally obtain a film with a first coating;
and 5: and (3) sputtering a second coating layer on the film: putting the film with the first coating into a drying box for fully drying; after drying, sputtering aluminum particles on the surface of the film by a magnetron sputtering method, and forming a second coating on the surface of the first coating after sputtering;
step 6: the film with two layers of coatings was subjected to the following treatment process:
(1) curling treatment: feeding the film into a plurality of curling rollers which are arranged in a vertical crossed way, and repeatedly curling the film;
(2) dry wiping treatment: during the curling process, the dry wiping roller transmits the dry wiping material to the curling part above the curling roller, and when the area to be wiped is transmitted to the roller, the dry wiping roller moves downwards quickly, so that the dry wiping material is separated after rapidly contacting the area to be wiped of the film, the dry wiping of the surface of the film is realized, and a dry wiping area is formed;
(3) wet wiping treatment: during the curling treatment, the wet wiping roller transmits wet wiping materials to the curling part above the curling roller, and when the area to be wiped is transmitted to the roller, the wet wiping roller moves downwards quickly, so that the wet wiping materials are separated after rapidly contacting the area to be wiped of the film, the wet wiping on the surface of the film is realized, and a wet wiping area is formed;
(4) heating treatment: when the curling treatment, the dry wiping treatment and the wet wiping treatment are carried out, a temperature control device is utilized to control the environment temperature to respectively reach the starting temperature, the normal working temperature and the limit working temperature of the conventional lithium battery;
and 7: the coating was examined and analyzed:
(1) after the dry wiping is finished, shooting an image of the dry wiping material by using a first inspection camera, and comparing the image with a standard image so as to judge the dry wiping stability of the coating of the film;
(2) after wet wiping is finished, shooting an image of the wet wiping material by using a second inspection camera, and comparing the image with a standard image so as to judge the wet wiping stability of the coating of the film;
(3) after the curling treatment, the dry wiping treatment and the wet wiping treatment are finished, a dry wiping area, a wet wiping area and a non-wiping area of the film are irradiated by structured light, corresponding images are shot by a third camera and are compared with standard images of three areas stored in advance, and therefore the comprehensive stability of the film coating is determined;
and (4) integrating dry wiping stability, wet wiping stability and integrated stability to obtain the falling risk condition of the film coating.
2. The method of claim 1, wherein: wherein the thickness of the first coating layer is controlled to be 2-3 μm.
3. The method of claim 1, wherein: wherein the thickness of the second coating layer is controlled to be 0.5-0.8 μm.
4. The method of claim 1, wherein: the step-by-step drying comprises 45 ℃, 50 ℃, 60 ℃ and 65 ℃.
5. A fluoropolymer composite coated polyethylene film characterized by: prepared using a process as claimed in any preceding claim.
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Denomination of invention: Polyethylene film with fluoropolymer composite coating and its preparation method

Effective date of registration: 20220607

Granted publication date: 20201229

Pledgee: Weihui Investment Group Ltd.

Pledgor: Henan functional polymer membrane material innovation center Co.,Ltd.

Registration number: Y2022980007174