CN101724168A - Preparation method of polyolefin microporous membrane - Google Patents
Preparation method of polyolefin microporous membrane Download PDFInfo
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- CN101724168A CN101724168A CN200910109633A CN200910109633A CN101724168A CN 101724168 A CN101724168 A CN 101724168A CN 200910109633 A CN200910109633 A CN 200910109633A CN 200910109633 A CN200910109633 A CN 200910109633A CN 101724168 A CN101724168 A CN 101724168A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion 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
- B29C48/09—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels
- B29C48/10—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels flexible, e.g. blown foils
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92561—Time, e.g. start, termination, duration or interruption
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92857—Extrusion unit
- B29C2948/92876—Feeding, melting, plasticising or pumping zones, e.g. the melt itself
- B29C2948/92895—Barrel or housing
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92923—Calibration, after-treatment or cooling zone
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92942—Moulded article
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/04—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets uniaxial, e.g. oblique
- B29C55/08—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets uniaxial, e.g. oblique transverse to the direction of feed
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/18—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets by squeezing between surfaces, e.g. rollers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/28—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of blown tubular films, e.g. by inflation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/04—Condition, form or state of moulded material or of the material to be shaped cellular or porous
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/755—Membranes, diaphragms
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
Abstract
The invention provides a preparation method of polyolefin microporous membrane, comprising the following steps of: (1) mixing polyolefin resin and diluent according to the weight percent ratio of 10-60%:40-90%; (2) extruding and molding the mixture in an extrusion-blow molding manner to form bubble and cooling; (3) sizing the superposed and drawn membrane; (4) extracting diluent and drying; (5) performing transverse stretching and sizing treatment; and (6) rolling. By adopting the method of forming the bubble in a blow molding way, the invention avoids uneven structure caused by different cooling on the both surfaces in the casting process of general bidirectional stretching technique as well as uneven structure caused by slippage during longitudinal stretching, solves the problem of slippage of rollers during longitudinal stretching and ensures balanced longitudinal and transverse properties to finally obtain the polyolefin microporous membrane with even structure. Besides, the invention has the advantages of little investment, small occupation area, no slitter edge, easily-controlled production field, and the like.
Description
Technical field
The present invention relates to a kind of preparation method of plastics film, relate in particular to a kind of preparation of microporous polyolefin film.
Background technology
Microporous polyolefin film is the micropore with countless intercommunications, and the aperture is the plastics film of 0.01～10 μ m.Its preparation method mainly contains: high filled plastics membrane process, fusion drawn method, thermally induced phase separation, tubular fibre method, physical mechanical perforation method etc. stretch.Wherein industrialized method mainly contains fusion drawn method and thermally induced phase separation.
The fusion drawn method is earlier with crystalline polymer (as polypropylene) extrusion molding film forming under the condition that improves molten polymer stress, make film under no tension force or low-tension, obtain the necessary crystallization structure then through annealing, after carry out the reticulated structure that longitudinal stretching produces a kind of slit-shaped space.There are shortcomings such as aperture and the difficult control of porosity in this method, and owing to only carry out longitudinal stretching, the film transverse strength is relatively poor.Specifically describe visible U.S.Patent 3558764 (1971), 5385777 (1995).
Thermally induced phase separation (TIPS) is at high temperature as in the twin screw extruder polymkeric substance (as HDPE) to be dissolved in high boiling point, solvent (the thinner of low volatility, as mineral oil), form uniform solution, back through port mould extrusion moulding sheet, quenching cooling on chill roll, causing solution to produce is separated, obtain having the sheet of phase separation structure, the back adopts two-way stretch equipment while or proceed step by step in length and breadth to stretching, acquisition has the film of phase separation structure, wherein before or after two-way stretch, adopt volatile organic solvent (extraction agent) that thinner is extracted, thereby obtain the high molecule micropore of certain structural shape.Asahi-Kasei, the Mitsui Chemical of Japan and relevant patent JP 2004323820 (2004), the U.S.Patent 6245272 (2001) of Tonen company have reported this method.Also introduced technology and the prescription of producing microporous membrane according to thermally induced phase separation in the patent documentations such as Patent Office of the People's Republic of China disclosed 200410051437.4,200510035680.1.
Producing in the microporous membrane process at the foundation thermally induced phase separation in above-mentioned all patents all is to adopt vertically horizontal substep two-way stretch or the synchro-draw in back earlier.In the step drawing process, because the existence of Macrodilution agent in the prescription, after thermal induction is separated, there is Macrodilution agent liquid on casting sheet surface, enter behind the longitudinal stretching roller between roller in the drawing process and to cause owing to skidding that final microporous membrane structure is inhomogeneous, thickness deviation is big; And be pulled through in the journey horizontal afterwards, because the horizontal inherent tensile properties that draws, the thick intermediate thin in the horizontal both sides of film causes structure inhomogeneous equally.And in the synchro-draw process, though solved the problem of skidding of longitudinal stretching, the same with step drawing on the one hand, need the excision slitter edge, the product recovery rate is low, and equipment is invested greatly comparatively speaking on the other hand.
Summary of the invention
The purpose of the embodiment of the invention be to provide a kind of invest little, easy to control, membrane structure evenly, the method for producing microporous polyolefin film of slitter edge free.
The embodiment of the invention is achieved in that a kind of method for preparing polyolefin microporous membrane, comprises the steps:
1), with polymer matrix material---polyolefin resin and mixing diluents, described polyolefin resin and thinner weight ratio are 1-6: 4-9.Amount of diluent is too little, and the film porosity that obtains is not enough, and content is too many, one side forming process difficulty, and film bubble homogeneity and stability are not enough, and film strength is not enough on the other hand.
2), the molten resin extruded from forcing machine makes pipe through the circular clearance head, adopts the extrusion-blown modling mode by the forcing machine annular die said mixture extrusion-blown modling to be formed film bubble postcooling, forms tubular film.Blow molding is one of common film-forming method, has been widely used in thermoplastic films' such as PP, PE, PVC, PVDC, PET, PBT, PA the commercial process.
3), the film after the superimposed traction is done typing after the cooling and handles, this also is the common technology of field of thin film fabrication.
4), thinner and carry out drying treatment in the spe membrane;
5), cross directional stretch typing is handled: with film at softening temperature to a certain temperature condition between the melt temperature, stretch along horizontal direction, and keeping under the tension force situation, be lower than being higher than its draft temperature in the temperature range of fusing point and keep several seconds under certain suitable temperature, be cooled to room temperature at last.
6), rolling.
In the technical scheme of the invention described above, described polyolefin resin is a kind of in high density polyethylene(HDPE), medium-density polyethylene, new LDPE (film grade), linear low density polyethylene, ultrahigh molecular weight polyethylene(UHMWPE), polypropylene, ethene and propylene or butylene, octene, the hexene copolymer, or the mixture of above-mentioned substance.The preferred high density polyethylene(HDPE) of said polyolefins resin material (HDPE), this is a kind of degree of crystallinity height, nonpolar thermoplastic resin, and is non-hygroscopic and have good steam-preventing, and has good electrical property.
Thinner of the present invention is selected for use at high temperature has the high boiling point of excellent compatibility, difficult evaporable solvent with polyolefin resin, can be hydrocarbon polymer: nonane, how alkane, whiteruss, solid paraffin; Or be ester compound: dioctyl phthalate (DOP), dibutyl phthalate, stearate; Or the mixture of above-claimed cpd.Preferred liquid paraffin in the above-mentioned thinner, between the viscosity 70～120cst of whiteruss, viscosity is too high, is difficult for being extracted the agent extraction, and viscosity is too low, and the blow-moulding process bubble stability is not enough.
Particularly, described step 1) needs to mix by high mixer earlier when adopting multiple polyolefin resin to mix, or in Banbury mixer or forcing machine, carry out, the preferred twin screw extruder of forcing machine, further carry out with being blended under 180～240 ℃ of thinner afterwards, the mixing temperature of described polyolefin resin and thinner is 180～240 ℃.
Particularly, described step 2) 180～240 ℃ of the die temperatures during by forcing machine annular die extrusion moulding film bubble with the polymkeric substance that mixes and diluent solution, annular die gap 0.6～2mm, the film bubble that leaves mouthful mould adopts air ring or water cooling, and bubbling air propels the price of, propel the price of than 1～5 times 1～5 times of draw ratio.
Particularly, 100～150 ℃ of the treatment temps when described step 3) is finalized the design processing through the superimposed laggard row of the film that propels the price of traction, treatment time 1～100s.
Particularly, extraction agent in the described step 4) is selected for use with thinner has good consistency, and and a kind of in inconsistent hydro carbons, hydrochloric ether, fluorinated hydrocarbons or the ketones solvent between the polyolefin resin, or adopt non-inflammable and explosive and not halogen-containing organic solvent with height Environmental Safety.Wherein, described varsol is pentane, hexane, heptane, decane, hydrochloric ether is trichloromethane or tetracol phenixin, and ketones solvent is acetone or butanone, and described organic solvent is diethylene glycol dimethyl ether, dihydroxy ethyl butyl ether, diethylene glycol monoethyl ether or diethylene glycol diethyl ether.At first extract microporous polyolefin film during extraction and produce raw materials used high boiling point thinner, after adopt again that volatile and non-inflammable and explosive solvent cleans film under the normal temperature, this kind solvent down after the volatilization, stays microvoid structure in normal temperature or heated condition in film.
For further improving microvoid structure in the film, described step 5) is carried out the cross directional stretch typing and is handled 100～150 ℃ of wherein heat setting type treatment temps, 1～100 second treatment time, 1～1.5 times of stretching ratio.
As of the present invention further, in the described step 1), also can be added with and to improve wear resistance, improve the filler of the follow-up use properties of microporous membrane, described filler proportion is 5～15% of a gross weight, described filler can be selected a kind of in silicon-dioxide, titanium dioxide, the lime carbonate or their mixture, the excellent silicon-dioxide of preferred surface treated dispersiveness for use.
As further of the present invention, in the described step 1), also nucleator can be added or/and oxidation inhibitor, described nucleator proportion is 1～5% of a gross weight, described oxidation inhibitor proportion be gross weight 0.1～0.5%), described nucleator is selected a kind of or mixture in aliphatic carboxylic acid metal compound, sorbyl alcohol benzal derivative, aromatic carboxylic acid metallic compound, organophosphate and xylonic acid and derivatives class, Sodium Benzoate and two (p-tert-butyl benzoic acid) carboxyl aluminium etc. for use, and oxidation inhibitor selects for use in the polyolefine commonly used 1010 or 1076 and 168 to be used.Wherein said nucleator can promote the crystallisation process of molecule and accelerate crystallization velocity, improve crystallinity of polymer, thereby improve hardness, Young's modulus, tensile strength, the yield strength of plastics, also can prevent plastics post crystallization phenomenon, thereby improve the dimensional stability of goods.Described oxidation inhibitor can suppress or delay the oxidative degradation of plastics and prolong its work-ing life, can improve the plastics film quality.
To sum up, the present invention is according to the thermal induction mechanism that is separated, in the process of making microporous polyolefin film, adopt the method for blow molding film bubble, avoided casting sheet process because the structure non-uniform phenomenon that two surface cool differences cause, the structure non-uniform phenomenon of also having avoided the longitudinal stretching process to skid and cause finally can obtain the microporous polyolefin film of even structure.And, compare vertical earlier horizontal step drawing in back or synchro-draw process, blow molding has advantages such as investment is little, floor space is little, slitter edge free, the easy control in production scene, be applied in the microporous polyolefin film preparation process, solved the longitudinal stretching process roller problem of skidding, to balancing performance, therefore more show its advantage in length and breadth.
Embodiment
In order to make purpose of the present invention, technical scheme and advantage clearer,, the present invention is further elaborated below in conjunction with embodiment.Should be appreciated that specific embodiment described herein only in order to explanation the present invention, and be not used in qualification the present invention.
Embodiment 1:
The high density polyethylene(HDPE) (133 ℃ of fusing points) of 10% (weight) is dropped into twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type) in, the whiteruss (kinematic viscosity 90cst/40 ℃) that adds 90% (weight) with volume pump by the side direction spout, at 200 ℃, melting mixing is modulated into solution under 150 rev/mins the condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 200 ℃ of die head temperatures), the blow molding film steeps and cools off by air ring, propel the price of than 1, draw ratio 1, the typing of superimposed back is handled, 100 ℃ of treatment temps, treatment time 10s; The whiteruss in the butanone extraction film is adopted in the back, and dry back is 100 ℃ of processing of finalizing the design, and 1.0 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment 2:
The polypropylene (167 ℃ of fusing points) of 60% (weight) is dropped in the twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type), the solid paraffin that adds 40% (weight) with volume pump by the side direction spout, melting mixing is modulated into solution under 200 ℃, 150 rev/mins condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 180 ℃ of die head temperatures), the blow molding film steeps and cools off by air ring, propel the price of than 5, draw ratio 5, the typing of superimposed back is handled, 150 ℃ of treatment temps, treatment time 100s; The whiteruss in the butanone extraction film is adopted in the back, and dry back is 150 ℃ of processing of finalizing the design, and 1.5 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment 3:
The high density polyethylene(HDPE) (133 ℃ of fusing points) of 20% (weight) is dropped in the twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type), the dioctyl phthalate (DOP) that adds 80% (weight) with volume pump by the side direction spout, melting mixing is modulated into solution under 200 ℃, 150 rev/mins condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 240 ℃ of die head temperatures), the blow molding film steeps and cools off by air ring, propel the price of than 3, draw ratio 3, the typing of superimposed back is handled, 125 ℃ of treatment temps, treatment time 10s; The dioctyl phthalate (DOP) in the butanone extraction film is adopted in the back, and dry back is 125 ℃ of processing of finalizing the design, and 1.4 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment 4:
The polypropylene (167 ℃ of fusing points) of 30% (weight) is dropped in the twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type), the stearate that adds 70% (weight) with volume pump by the side direction spout, melting mixing is modulated into solution under 200 ℃, 150 rev/mins condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 200 ℃ of die head temperatures), the blow molding film steeps and cools off by air ring, propel the price of than 2, draw ratio 2, the typing of superimposed back is handled, 140 ℃ of treatment temps, treatment time 50s; The stearate in the dichloromethane extraction film is adopted in the back, and dry back is 140 ℃ of processing of finalizing the design, and 1.3 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment 5:
Medium-density polyethylene with 15% (weight), the linear low density polyethylene of 15% (weight) (115 ℃ of fusing points) is put into high mixer and is mixed back input twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type) in, the whiteruss (kinematic viscosity 90cst/40 ℃) that adds 70% (weight) with volume pump by the side direction spout, at 200 ℃, melting mixing is modulated into solution under 150 rev/mins the condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 200 ℃ of die head temperatures), the blow molding film steeps and cools off by air ring, propel the price of than 3, draw ratio 1, the typing of superimposed back is handled, 120 ℃ of treatment temps, treatment time 70s; The whiteruss in the diethylene glycol dimethyl ether extraction film is adopted in the back, and dry back is 120 ℃ of processing of finalizing the design, and 1.2 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment 6:
The high density polyethylene(HDPE) (133 ℃ of fusing points) of 30% (weight) is dropped into twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type) in, the whiteruss (kinematic viscosity 90cst/40 ℃) that adds 65% (weight) with volume pump by the side direction spout, add 5% silica filler simultaneously, at 200 ℃, melting mixing is modulated into solution under 150 rev/mins the condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 200 ℃ of die head temperatures), blow molding film bubble also adopts water-cooled, propel the price of than 3, draw ratio 3,125 ℃ of treatment temps, treatment time 10s are handled in the typing of superimposed back; The whiteruss in the butanone extraction film is adopted in the back, and dry back is 125 ℃ of processing of finalizing the design, and 1.4 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment 7:
The polypropylene (167 ℃ of fusing points) of 30% (weight) is dropped into twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type) in, the whiteruss (kinematic viscosity 90cst/40 ℃) that adds 65% (weight) with volume pump by the side direction spout, add 3% silicon-dioxide simultaneously, 1.8% Sodium Benzoate nucleator, 0.2% 1010/168 oxidation inhibitor, at 230 ℃, melting mixing is modulated into solution under 150 rev/mins the condition, this solution is passed through annular die head (die lip opening degree 0.8mm, 230 ℃ of die head temperatures), the blow molding film steeps and cools off by air ring, propel the price of than 3, draw ratio 3,145 ℃ of treatment temps, treatment time 10s are handled in the typing of superimposed back; The whiteruss in the butanone extraction film is adopted in the back, and dry back is 145 ℃ of processing of finalizing the design, and 1.4 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Comparative example 1:
The high density polyethylene(HDPE) (133 ℃ of fusing points) of 30% (weight) is dropped in the twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type), the whiteruss (kinematic viscosity 90cst/40 ℃) that adds 70% (weight) with volume pump by the side direction spout, melting mixing is modulated into solution under 200 ℃, 150 rev/mins condition, by T shape die head (die lip opening degree 0.8mm), chilling casting sheet obtains sheet with this solution.Sheet is carried out preheating, and 120 ℃ of preheating temperatures are carried out respectively in length and breadth to stretching, stretch ratio 3 * 3, and typing is handled, 125 ℃ of treatment temps, treatment time 10s; The whiteruss in the butanone extraction film is adopted in the back, and dry back is 125 ℃ of processing of finalizing the design, and 1.4 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Comparative example 2:
The polypropylene (167 ℃ of fusing points) of 30% (weight) is dropped in the twin screw extruder (diameter 78mm, L/D=50, strong mixed milling type), the whiteruss (kinematic viscosity 90cst/40 ℃) that adds 70% (weight) with volume pump by the side direction spout, melting mixing is modulated into solution under 200 ℃, 150 rev/mins condition, by T shape die head (die lip opening degree 0.8mm), chilling casting sheet obtains sheet with this solution.Sheet is carried out preheating, and 140 ℃ of preheating temperatures are carried out respectively in length and breadth to stretching, stretch ratio 3 * 3, and typing is handled, 145 ℃ of treatment temps, treatment time 10s; The whiteruss in the butanone extraction film is adopted in the back, and dry back is 145 ℃ of processing of finalizing the design, and 1.4 times of stretching ratios make rolling behind the microporous polyolefin film finished product.
Embodiment and comparative example comparative result see Table 1.
Table 1
| Example 1 | Example 2 | Example 3 | Example 4 | Example 5 | Example 6 | Example 7 | Comparative example 1 | Comparative example 2 | |
| Thickness um | ??20 | ??20 | ??20 | ??20 | ??20 | ??20 | ??20 | ??20 | ??20 |
| Porosity % | ??40 | ??35 | ??45 | ??40 | ??40 | ??42 | ??42 | ??45 | ??45 |
| Gas permeability sec/100ml | ??450 | ??650 | ??380 | ??480 | ??490 | ??450 | ??460 | ??550 | ??530 |
The embodiment of the invention is compared as can be seen with comparative example 1,2, it in the comparative example 1 and 2 conventional elder generation's horizontal biaxial orientation process in vertical back, owing to vertical be pulled through skidding and casting the inhomogeneous of sheet process two surface tissues of journey, the Gas permeability of final microporous membrane is high slightly, to cast the blow molding technology that sheet and two-way stretch combine and adopt, under technology, prescription synergy, the structure non-uniform phenomenon of having avoided the problems referred to above to cause, Gas permeability has certain improvement.
The above only is preferred embodiment of the present invention, not in order to restriction the present invention, all any modifications of being done within the spirit and principles in the present invention, is equal to and replaces and improvement etc., all should be included within protection scope of the present invention.
Claims (11)
1. a method for preparing polyolefin microporous membrane is characterized in that, comprises the steps:
1), with polyolefin resin and mixing diluents, described polyolefin resin and thinner weight ratio are 1-6: 4-9;
2), adopt the extrusion-blown modling mode that said mixture extrusion-blown modling is formed film bubble postcooling;
3), the film after the superimposed traction being done typing handles;
4), extraction thinner and dry;
5), the cross directional stretch typing is handled;
6), rolling.
2. a kind of method for preparing polyolefin microporous membrane according to claim 1, it is characterized in that, described polyolefin resin is a kind of in high density polyethylene(HDPE), medium-density polyethylene, new LDPE (film grade), linear low density polyethylene, ultrahigh molecular weight polyethylene(UHMWPE), polypropylene, ethene and propylene or butylene, octene, the hexene copolymer, or the mixture of above-mentioned substance.
3. a kind of method for preparing polyolefin microporous membrane according to claim 1 is characterized in that, described thinner is a hydrocarbon polymer: nonane, how alkane, whiteruss, solid paraffin; Or be ester compound: dioctyl phthalate (DOP), dibutyl phthalate, stearate; Or the mixture of above-claimed cpd.
4. a kind of method for preparing polyolefin microporous membrane according to claim 2, it is characterized in that, in the described step 1), need when adopting multiple polyolefin resin mix by high mixer earlier, or in Banbury mixer or forcing machine, carry out, further carry out with being blended under 180～240 ℃ of thinner afterwards, the mixing temperature of described polyolefin resin and thinner is 180～240 ℃.
5. a kind of method for preparing polyolefin microporous membrane according to claim 1, it is characterized in that, described step 2) in, the polymkeric substance and the diluent solution that mix are steeped by forcing machine annular die extrusion moulding film, and wherein die temperature is 180～240 ℃, annular die gap 0.6～2mm, the film bubble that leaves mouthful mould adopts air ring or water cooling, and bubbling air propels the price of, and propels the price of than 1～5 times 1～5 times of draw ratio.
6. a kind of method for preparing polyolefin microporous membrane according to claim 1 is characterized in that, in the described step 3), 100～150 ℃ of treatment temps, treatment time 1～100s are handled in superimposed laggard row typing through the film that propels the price of traction.
7. a kind of method for preparing polyolefin microporous membrane according to claim 1, it is characterized in that, extraction agent in the described step 4) is a kind of in hydro carbons, hydrochloric ether, fluorinated hydrocarbons or the ketones solvent, or adopts non-inflammable and explosive and not halogen-containing organic solvent with height Environmental Safety.
8. a kind of method for preparing polyolefin microporous membrane according to claim 7, it is characterized in that, described varsol is pentane, hexane, heptane, decane, hydrochloric ether is trichloromethane or tetracol phenixin, ketones solvent is acetone or butanone, and described organic solvent is diethylene glycol dimethyl ether, dihydroxy ethyl butyl ether, diethylene glycol monoethyl ether or diethylene glycol diethyl ether.
9. a kind of method for preparing polyolefin microporous membrane according to claim 1, it is characterized in that described step 5) is also carried out the cross directional stretch typing and handled 100～150 ℃ of wherein heat setting type treatment temps after above-mentioned extraction, 1～100 second treatment time, 1～1.5 times of stretching ratio.
10. a kind of method for preparing polyolefin microporous membrane according to claim 1 is characterized in that, in the described step 1), also is added with 5～15% fillers, and described filler is a kind of in silicon-dioxide, titanium dioxide, the lime carbonate or their mixture.
11. according to claim 1 or 9 described a kind of method for preparing polyolefin microporous membrane, it is characterized in that, in the described step 1), also be added with 1～5% nucleator or/and 0.1～0.5% oxidation inhibitor, described nucleator is selected a kind of in aliphatic carboxylic acid metal compound, sorbyl alcohol benzal derivative, aromatic carboxylic acid metallic compound, organophosphate and xylonic acid and derivatives class, Sodium Benzoate and the two carboxyl aluminium etc. or their mixture for use, and described oxidation inhibitor selects for use in the polyolefine commonly used 1010 or 1076 and 168 to be used.
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| PCT/CN2010/078752 WO2011057587A1 (en) | 2009-11-16 | 2010-11-15 | Preparation method of polyolefin microporous membrane |
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| WO2011057587A1 (en) * | 2009-11-16 | 2011-05-19 | 深圳市星源材质科技股份有限公司 | Preparation method of polyolefin microporous membrane |
| CN102241832A (en) * | 2011-05-14 | 2011-11-16 | 中材科技股份有限公司 | Polyolefin film and preparation method thereof |
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| CN101724168B (en) * | 2009-11-16 | 2011-09-21 | 深圳市星源材质科技股份有限公司 | Preparation method of polyolefin microporous membrane |
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2009
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| CN101724168B (en) | 2011-09-21 |
| WO2011057587A1 (en) | 2011-05-19 |
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