Patent Application
20180036933
This disclosure relates to a method for producing a microporous plastic film.
Microporous plastic films have been broadly used as a substance separation membrane, permselective membrane, separator material of electrochemical element such as alkali rechargeable battery, lithium rechargeable battery, fuel cell and capacitor or the like. A separator for lithium ion battery is a particularly suitable application.
JP 2009-249480-A and JP 2013-530261-A disclose a wet process for producing a microporous film made of plastic like polyolefin. In the wet process, a diluent such as liquid paraffin is added to a resin, and is kneaded and dispersed, and then discharged through a die lip onto a cooling drum to be cooled and solidified to form a gel sheet, which is oriented uniaxially or biaxially by a roller method or tenter method to improve strength to produce a film having micropores by extracting the diluent.
Particularly by the roller method drawing the sheet in the travelling direction by a plurality of rollers, the lengthwise draw ratio can be changed freely by only changing a roller speed. By the other tenter method, the microporous plastic film can be improved in mechanical property because polyolefin molecules can be oriented with strong orientation in the drawing direction. As disclosed in JP 2009-249480-A, the roller method applied to the wet process might make the diluent bleed out from a gel sheet surface under a pressure caused by heat or tension while the conveying and drawing are performed in the presence of the diluent between film and roller. To draw such a gel sheet, the sheet is sufficiently cooled below the crystallization ending temperature of the resin and is heated again below the melting point as disclosed in JP 2013-530261-A where it is heated above the crystallization dispersion temperature.
The wet roller method disclosed in JP 2009-249480-A might have a problem that the diluent intervening between the roller and film lubricates to meander or fail a desirable draw ratio because of slip.
According to JP 2009-249480-A, the above-described slip can be prevented when a tension over the lengthwise draw tension is given between the lengthwise drawing machine and the lateral drawing machine (tenter), wherein the tension should preferably be greater than the draw tension by 20%. However, we found that such a great tension over the draw tension drew the sheet downstream of the lateral drawing machine to cause an undesirable slip adversely and therefore the slip couldn't be prevented.
According to JP 2013-530261-A, a predetermined range of contact time, contact angle and contact length between the lengthwise drawing roller and the sheet can prevent the slip and the sheet surface from being damaged. However, we found even such measures couldn't fully prevent the slip when we had an increased draw speed, a decreased draw temperature or an increased draw ratio in order to improve physical properties and mechanical properties of the microporous plastic film.
Accordingly, it could be helpful to provide a method of producing a microporous plastic film excellent in physical properties and mechanical properties by a high-speed drawing without slip under a high productivity.
Our method of producing a microporous plastic film comprises: kneading a diluent and a polyolefin resin with an extruder; discharging the polyolefin resin kneaded with the diluent from a die lip in a sheet shape; cooling and solidifying the sheet discharged from the die lip on a drum; reheating and drawing the solidified sheet with a plurality of rollers in a sheet conveying direction; cooling the sheet drawn in the sheet conveying direction; gripping both ends of the sheet with clips; introducing the sheet into a tenter; and washing the diluent out to prepare a uniaxially or biaxially oriented microporous plastic film, wherein the method, wherein the method further comprises pressing the sheet interposing between a nip roller having a surface coated with a rubber and a driving roller driven by a motor upstream from a roller at the most downstream side among the rollers, wherein number N of pairs of the driving roller and the nip roller satisfies the following formula:
N>T/(μ·P), where
T [N]: drawing tension required for drawing sheet in sheet conveying direction,
μ: coefficient of friction between driving roller sheet, and
P [N]: nip pressure between driving roller and nip roller.
Another of our methods of producing a microporous plastic film comprises: kneading a diluent and a polyolefin resin with an extruder; discharging the polyolefin resin kneaded with the diluent from a die lip in a sheet shape; cooling and solidifying the sheet discharged from the die lip on a drum; reheating and drawing the solidified sheet with a plurality of rollers in a sheet conveying direction; cooling the sheet drawn in the sheet conveying direction; gripping both ends of the sheet with clips; introducing the sheet into a tenter; and washing the diluent out to prepare a uniaxially or biaxially oriented microporous plastic film, wherein the method, wherein the method further comprises pressing the sheet interposing between a nip roller having a surface coated with a rubber and a driving roller driven by a motor upstream from a roller at the most downstream side among the rollers, wherein 5 or more pairs of the driving roller and the nip roller are provided.
It is preferable that the driving roller has a surface made of a metal or a ceramic and has a surface roughness less than 1 S.
“Nip” means to press a sheet as being interposed with rollers. “Nip roller” means one of the two rollers used to press the sheet interposing therebetween, the one being pressed onto the other one facing to the one by moving to press the sheet interposing therebetween.
We can produce, with high productivity, a microporous plastic film having excellent physical properties and mechanical properties by preventing slip even in wet roller drawing.
Hereinafter, desirable examples of our microporous plastic film will be explained with reference to figures.
To desirably produce microporous plastic film 11, polyolefin resin is mixed with diluent and heated to melt and prepare a polyolefin solution. The diluent creates a structure forming micropores of the microporous plastic film and contributes to improvement of drawability (for example, improvement as reduction of unevenness at a draw ratio for exhibiting a strength) at the time of drawing film.
The diluent is not limited particularly, as far as it can be mixed or dissolved with polyolefin resin. The diluent may be mixed with polyolefin in a melt-kneading state. Alternatively, it may be mixed with solid solvent at room temperature. Such prepared solid diluent may be stearyl alcohol, ceryl alcohol, paraffin wax or the like. It is preferable that the diluent is a liquid at room temperature from the viewpoints of prevention of uneven drawing and coating convenience at a later stage. The liquid diluent may be a fatty series such as nonane, decane, decalin, paraxylene, undecane, dodecane and liquid paraffin; a cyclic fatty series or an aromatic hydrocarbon; a mineral oil fraction having a boiling point of the same range as the compounds thereof; or a phthalate ester such as dibutyl phthalate and dioctylphthalate which are liquids at room temperature. To obtain a gelled sheet stably containing liquid diluent, it is preferable to employ a nonvolatile diluent such as liquid paraffin. For example, it is preferable that the liquid diluent has a viscosity of 20 to 200 cSt at 40° C.
It is preferable that the polyolefin resin of 10 to 50 mass % is mixed with the diluent in total 100 mass % of polyolefin resin and diluent, from a view point of good formability of extruded product. The polyolefin resin solution may be melt-kneaded uniformly by a calendar, mixer or extruder 21 having a screw as shown in
It is preferable that the polyolefin resin solution in extruder has a predetermined temperature of 140 to 250° C. for a polyethylene composition and 190 to 270° C. for a polypropylene-containing composition, as depending on resin kind. A thermometer is provided inside the extruder or in a cylinder section to indirectly monitor temperature and properly adjust the heater temperature, rotation speed and discharge rate of the cylinder section to control the temperature in a target range.
The polyolefin resin solution which has been melt-kneaded by extruder 21 is discharged through a slit section of die lip 23 into a sheet while it is measured with gear pump 22 as needed. Such discharged gelled sheet 12 is solidified as contacting first cooling drum 31. Gelled sheet 12 becomes a pillar part with a crystal structure made of the polyolefin supporting pores of macroporous plastic film 11. Gelled sheet 12 becomes in a gel state since it includes the diluent melt-kneaded in extruder 21. A part of the diluent bleeds out from sheet surface by cooling gelled sheet 12 so that the sheet with a wet surface made by the diluent is conveyed on first cooling drum 31.
The thickness of gelled sheet 12 can be adjusted by adjusting the cooling drum speed relative to the flow rate from the die lip slit section according to discharge rate.
It is preferable that first cooling drum 31 has a temperature of 15 to 40° C., which may affect on the crystal structure of gelled sheet 12. It is because the final cooling temperature should be below the crystallization ending temperature. The molecular orientation tends to advance in a later drawing process when the higher-order structure is fine. To make up for cooling time, it is possible, that the diameter of first cooling drum 31 is enlarged, second cooling drum 32 is added to first cooling drum 31 or a plurality of cooling drums are further added. To make the crystal structure precise and uniform in gelled sheet 12, it is preferable that a parameter such as conveyance speed, drum temperature, drum size and the number of drums, is designed in view of the cooling speed. For example, even when a target sheet temperature is 30° C., first cooling drum 31 may be around 20° C. because too high a speed might cause insufficient heat conduction. It is preferable that humidity is lowered by air conditioning when the temperature is below 25° C. First cooling drum 31 may have a shape of a roller or belt. It is preferable that a surface of first cooling drum 31 is made of metal, ceramic or fiber composite material, which is excellent in shape stability and working accuracy to keep the roller speed constant. It is particularly preferable that the surface is made of a metal which is excellent in heat conduction to a film. It is possible to perform non-adhesion coating or rubber coating on it to the extent that conduction is not obstructed. It is preferable that the surface of sheet and roller are made of metal including metal plating which is excellent in scratch resistance and heat conductivity and is not swelled by the bled-out diluent making wet state on the surface.
It is preferable that cooling drums 31 and 32 are provided with a conventional heat pump or cooling device in addition to an internal flow path for refrigerant to control the surface temperature. The roller is driven to rotate by a rotation driving means such as a motor at a predetermined speed while a speed-changing mechanism may be provided between rollers to apply draw tension or relaxation according to expansion and shrinkage of the sheet. Alternatively, each roller may be provided with a motor to achieve a function like the speed-changing mechanism by accurately adjusting the speed by inverter or servo.
In
To prevent wet gelled sheet 12 from meandering or degrading cooling efficiency by lubrication, it is possible that the sheet is pushed onto first cooling drum 31 with a contacting means such as nip roller, jet nozzle, suction chamber and electrostatic application. Such a contacting means can improve the travelling property and cooling efficiency of gelled sheet 12 to enable easy setting of the cooling speed and the final cooling temperature.
Other than cooling drum 31, it is preferable that gelled sheet 12 is depressed with a nip roller onto second cooling drum 32 or other conveying roller to increase coefficient of friction which has been decreased on the mirror surface. It is preferable that the surface of nip roller is made of rubber-like elastic material which can depress gelled sheet 12 uniformly onto uneven thickness of gelled sheet 12, deflection of roller and slight surface unevenness. The rubber-like elastic material is preferably a general vulcanized rubber such as Nitrile isoButylene-isoprene Rubber (NBR), Chloroprene Rubber (CR), Ethylene Propylene Rubber (EPDM) and Hypalon rubber (CSM). When gelled sheet 12 or conveying roller has a high temperature like 80° C. or higher, it is particularly preferable to employ the EPDM or CSM. Under a higher temperature, it is preferable to employ a silicone rubber or a fluorine rubber as well as the vulcanized rubber. It is preferable to employ a rubber which is little swelled by diluent to prevent the roller from having a distorted shape over time.
Next, gelled sheet 12 is oriented in a sheet-conveying direction with a plurality of roller groups in lengthwise drawing process 4, and then both ends of uniaxially oriented sheet 13 are gripped by a conventional clip to be oriented in a sheet width direction (direction orthogonal to the conveying direction) while the sheet is conveyed in the travelling direction while being heated and kept warm in an oven. In
Alternatively, like cooling drum 31, it is preferable that heating roller group 41 or drawing roller group 42 has an internal structure in which the roller is provided with a flow path for heat medium such as vapor and pressured hot water. It is possible that the roller is supported as rotatable with bearings and a shaft end connects to a heat-medium supply pipe with a rotary joint to supply heat medium without obstructing rotation of the roller to supply heat medium to the inside.
It is preferable that drawing is performed at a draw ratio of 5 to 12 in a sheet conveying direction although depending on the gelled sheet thickness. To improve strength and productivity, it is preferable that drawing is performed at an area ratio of 30 or more in a sheet width direction together with the sheet conveying-directional drawing. It is preferable that the area ratio is 40 or more, preferably 60 or more.
It is preferable that a drawing temperature is the melting point of polyolefin resin or less. It is preferable that the temperature is [crystal dispersion temperature Ted of polyolefin resin] to [melting point of polyolefin resin]. For example, it is preferable that the temperature is 80 to 130° C. for polyethylene resin, preferably 100 to 125° C. After drawing, a cooling process is performed down to these temperatures.
Thus performed drawing cleaves a higher order structure formed on the gelled sheet to miniaturize the crystal phase and form many fibrils. The fibrils are three-dimensionally connected irregularly to form a web structure. It is suitable for a battery separator because drawing improves mechanical strength and enlarges fine pores.
Thus obtained uniaxially oriented sheet 13 or biaxially oriented sheet 14 can be washed to remove diluent and dried up to make microporous plastic film 11 by a conventional technology as disclosed in WO2008/016174. To make microporous plastic film 11, it is possible that dry drawing process 7 is performed to reheat and re-draw the sheet after washing process 6. Re-drawing process 7 may be performed with a roller or a tenter. Also, heat treatment may be performed to adjust physical properties and remove residual distortion through the process. Depending on intended purposes, it is possible that the surface of microporous plastic film 11 is subject to a surface treatment such as corona discharge or functional coating with heat-resistant particles.
In
Although heating roller group 41 and drawing roller group 42 are common to each other in terms of heating and heat-keeping function of gelled sheet 12 and variable roller rotation speed, drawing roller group 42 comprises a roller to substantively draw gelled sheet 12 and generates a peripheral speed difference to permanently deform gelled sheet in the travelling direction. More particularly, drawing roller group 42 is defined as rollers which substantively draw it as generating 3% or more of peripheral speed difference relative to the upstream roller.
Gripping force (frictional force) is necessary between the roller and gelled sheet 12 to convey gelled sheet 12 without meandering in a travelling direction. Particularly in drawing roller group 42 where a high tension is generated by drawing, a high gripping force balancing the thawing tension is required to achieve a necessary draw ratio. The diluent having bled out as described above interposes between the roller and gelled sheet 12 in lubrication state to cause a deterioration of the gripping force required for conveyance and drawing.
When the drawing is performed between upstream drawing roller 421 and downstream drawing roller 422 in lengthwise drawing process 4, the drawing tension at the downstream side is balanced by receiving with the clip which grips the end of uniaxially oriented sheet 13 mainly in lateral drawing process 5. Although cooling roller group 43 may bear the drawing tension, it may not have a gripping force required to prevent the slip. Therefor; it is preferable that the roller group doesn't receive the tension to equal the speeds of lateral drawing process 5, downstream drawing roller 422 and uniaxially oriented sheet 13. It is preferable that the drawing roller such as drawing roller 422 in
On the other hand, the upstream drawing tension should be received by heating roller group 41 as well as upstream drawing roller 421 so that the total force thereof balances to the drawing tension. The upstream drawing tension should be balanced to these roller gripping forces. Otherwise, because there is no speed regulation section which is nonslip like tenter clip provided at the downstream side, the tension might be transmitted to molten gel sheet 12 between die lip 23 and first cooling drum 31 to cause problems such as varying thickness.
Accordingly, we obtain a gripping force balancing to the upstream drawing tension by pressing gelled sheet 12 interposing between a nip roller having a surface coated with rubber and a driving roller driven by a motor upstream from drawing roller 422 as the most downstream roller among drawing roller group 42 in
According to Coulomb's law, the nip pressure of nip roller generates friction force of each driving roller calculated by product μi·Pi, where μi is a coefficient of friction between each driving roller and sheet and Pi [N] is a nip pressure of nip roller provided on each driving roller. Not to transmit the tension to gelled sheet 12 discharged from the die lip, it is possible that the total of gripping force generated by the friction force is more than drawing tension T [N]. Because the friction force is generated only as a reactive force against the tension, gelled sheet 12 cannot be drawn upstream even with a force greater than the tension. This fact makes the following formula:
μ1·P1+μ2·P2+ . . . +μN·PN=Σμi·Pi>T
wherein i indicates a numbering ordinal to identify each driving roller like i=1 to N, wherein N pieces of driving rollers are necessary for the gripping. When the above-described inequality is satisfied, reactive force against the friction can be balanced to the drawing tension at the upstream side while reactive force against the friction of tenter clip can be balanced at the downstream side so that lengthwise drawing process 4 has no slip and no trouble such as meandering and insufficient drawing.
It is possible that drawing tension T is calculated from a sheet cross-section area sampled from a stress-distortion diagram made by a tension tester capable of displacing and measuring load after heating gelled sheet 12 which has been formed and cooled to a supposed drawing temperature in advance. The tension meter can be provided at any part from drawing roller group 42 to lateral drawing process 5.
Although nip pressure Pi can naturally be adjusted for each driving roller, it is conventionally known that the nip pressure is preferably 300 to 2,000 [N/m] per unit width to prevent meandering caused by excessively pressing with a pair of rollers. To calculate the number of nip rollers required for the gripping, the pressure can be assumed as constant at averaged value of pressure P. The above-described formula can be changed as follows:
μ1·P1+μ2·P2+ . . . +μN·PN=Σμi·Pi=P·Σμi>T.
Of course, coefficient of friction μi between each driving roller and gelled sheet 12 can have different values for each sheet and driving rollers. However, the measurement cannot be performed as conveying the sheet. So, gelled sheet 12 is sampled before drawing after forming and cooling in advance so that the measurement can be performed between gelled sheet 12 and a driving roller, plate or the like made of the same material as driving roller. The coefficient of friction may be measured by a conventional method disclosed by formula 2 and FIG. 5 of WO 2012/133097 pamphlet. The measurement of coefficient of friction is performed by hanging 2 kg weight on a sheet which has been cut into 100 mm width and wound by contact angle of 90° on the lengthwise drawing roller (of which surface is coated with hard chrome plating at 0.4 μm at the maximum height) not in operation at normal temperature of 25° C. The roller under suspension is monitored to be prevented from rotating by the suspended motor resistance in the measurement. Assuming that obtained measured value μ=constant, the formula becomes:
P·Σμi=P·μ·N>T.
Therefore, if number N of pairs of driving roller and nip roller, or the number of nip rollers is as follows, the gripping force at the upstream side to balance to the drawing tension can be ensured while lengthwise drawing process 4 under lubrication with diluent is prevented from having slip and meandering:
N>T/(μ·P).
For example, when the measured value range of μ is represented by the lower limit, N should be greater to increase the safety grade against slip but facility cost increases. When the range of μ is represented by the upper limit, N can be smaller to reduce facility cost but the slip might be caused by slight change of μ or increase of tension.
We found that it is possible that a polyethylene-based microporous plastic film is formed at a drawing tension per unit width T of 1000 to 4000 N/m and a coefficient of friction p around 0.05 to 0.4.
From a viewpoint of facility cost saving, when nip pressure P is set to 2,000 N/m which is the maximum in the desirable pressure range and when the coefficient of friction p is set to 0.4 in a case of relatively high friction, number N of nip roller pairs required to grip relatively high drawing tension of 4,000 N/m should be more than five pairs according to:
N>4,000/(0.4×2,000)=5 pairs.
It is more preferable that nip roller number N is normally 10 pairs or more, by assuming drawing tension T of 2,000 N/m, nip roller pressure of 1,000 N/m and μ of around 0.2. Because too many rollers may increase facility cost, it is preferable that N is 5 to 25 pairs, preferably 10 to 20 pairs.
With such a configuration, it is possible that the gripping force is exhibited by friction force from the heating roller to the upstream drawing roller as shown in
It is preferable that the surface of the nip roller is made of soft rubber-like elastic material that can depress gelled sheet 12 uniformly onto uneven thickness of gelled sheet 12, deflection of roller and slight surface unevenness. Because lengthwise drawing process 4 accompanies conveyance above the heat dispersion temperature in particular, the material is preferably a heat-resistant rubber such as EPDM and Hypalon rubber. It is preferably silicone rubber or fluoro-rubber. It is preferable to employ a rubber which is little swelled by diluent to prevent the roller from having a distorted shape over time.
It is possible that a nip is performed along a tangent line substantively with a nip roller to introduce gelled sheet 12 into heating roller or drawing roller as shown in
It is preferable that the roller has a surface roughness of 0.2 to 40 μm at the maximum height. To make a mirror surface, the surface roughness is preferably 0.2 to 0.8 μm. To make a sufficiently rough surface, the surface roughness is preferably 20 to 40 μm. Because the surface of the roller is wet with the diluent, the mirror surface has a low coefficient of friction caused by lubrication. The rough surface has an increased coefficient of friction caused by less or no lubrication because the diluent discharges from the unevenness. Although the mirror surface and the rough surface may be combined as needed, it is basically preferable that the mirror surface is provided from viewpoints of maintenance such as cleaning and speed control precision, preferably with a certain lubricant with diluent to prevent the sheet from having uneven appearance.
To prevent the surface of gelled sheet from being roughed by nipping when gripping force of nip roller is ensured, it is particularly preferable that the driving roller has a mirror surface of which maximum height is 1 S, or 1 μm or less, preferably 0.2 to 0.8 μm. To make such a mirror surface, the nip roller surface may be made of metal or ceramic as described above.
Hereinafter, our methods will be explained with reference to Examples although it is not limited to these Examples in particular.
A mixture is prepared by dry-blending of 0.375 parts by weight of tetrakis[methylene-3-(3,5-ditertiary butyl-4-hydroxyphenyl)-propionate]methane together with 100 parts by weight of polyethylene (PE) composition which comprises 40 mass % of ultrahigh molecular weight polyethylene having mass average molecular weight (Mw) of 2.5×106 and 60 mass % of high-density polyethylene having Mw of 2.8×105.
Thus obtained mixture is fed to twin-screw extruder 21 at flow rate of 97 kg/hr by a film forming method shown in
Thus obtained polyethylene solution is supplied into die lip 23 as being measured by a gear pump and the polyethylene solution at 210° C. is discharged on first cooling drum 31 adjusted to 35° C. by waterflow to form gelled sheet 12. First cooling drum 31 is driven to rotate at 10 m/min.
Gelled sheet 12 is subject to sampling with 10 mm square before introduction to lengthwise drawing process 4 to find that the thickness is 1.5 mm in 10 times average of contact-type thickness meter. Since bled-out diluent adheres to the surface, the above-described thickness measurement includes ±0.1 mm variation at the maximum.
Gelled sheet 12 is heated to 110° C. on the sheet surface with heating roller group 41 and a metal waterflow roller at the first roller of drawing roller group 42. Between heating roller group 41 and the first roller of each drawing roller group 42, the rotation speed of motor directly connected to the roller is controlled to make the downstream side faster by 1% of speed difference according to thermal expansion of the sheet. Drawing roller group 42 consists of 2 rollers shown in
Oriented film 13 is cooled on four rollers of cooling roller group 43 including last roller 422 of drawing roller group 42 to adjust the waterflow roller temperature to make the sheet temperature 50° C. Each clip speed difference between the last drawing roller, cooling roller group 43 and lateral drawing process is 0 to make the speed same.
From first cooling drum 31, surfaces of all rollers in lengthwise drawing process 4 are made of steel coated with hard chromic plating of which surface roughness is 10 μm (10 S) at the maximum height.
A preliminary sample has drawing tension T of 1,500N, nip roller pressure P of 2,000N and coefficient of friction μ of 0.15. Therefore, it becomes T/(μ×P)=1500/(0.15×20,000)=5. Therefore as shown in
Both ends of oriented film 13 are gripped with a clip to perform lateral drawing at draw ratio of 6 times at 115° C. in an oven, and then biaxially oriented film 14 cooled down to 30° C. is washed in a washing bath of methylene chloride kept at 25° C. to remove liquid paraffin. The washed film is dried up in a dry kiln kept at 60° C. and then is drawn again in redrawing process 7 at areal ratio of 1.2 times in lengthwise and lateral directions. The heat treatment is performed for 20 seconds by 90 m/min at 125° C. to prepare microporous plastic film 11 having thickness of 16 μm and width of 2,000 mm.
From first cooling drum 31, surfaces of all rollers in lengthwise drawing process 4 are made of steel coated with hard chromic plating of which surface roughness is 0.4 μm (0.8 S) at the maximum height. The other conditions are the same as Example 1.
As shown in
As shown in
The speeds of sheet and roller are measured by 1% accuracy including installation accuracy with a non-contact Doppler velocimeter (made by ACT Electronics Corp., model 1522). For all Examples and Comparative Examples, slip of film 11 before drawing is evaluated according to the following standards.
No good: The speed difference between roller and sheet is 10% or more of roller rotation speed.
Acceptable: The speed difference between roller and sheet is 5% or more and less than 10% of roller rotation speed.
Good: The speed difference between roller and sheet is less than 5% of roller rotation speed.
The amount of meandering in lengthwise drawing process 4 is evaluated according to the following standards.
No good: Meandering amount is 10 mm or more.
Acceptable: Meandering amount is 5 mm or more and less than 10 mm.
Good: Meandering amount is less than 5 mm.
The Gurley impermeability is determined according to JIS P8117 with Oken type Impermeability Tester (made by Asahi Seiko Co., Ltd., EGO-1T). The thrust strength is determined from the maximum load, applied when a needle having 1 mm diameter and spherical tip (Radius of curvature R=0.5 mm) is pricked at 2 mm/sec into a microporous membrane having membrane thickness T1. The measured maximum load La is converted to Lb which would be the maximum load when membrane thickness is 16 μm according to the following formula: Lb=(La×16)/T1 to calculate the thrust strength [N/16 μm].
Good: The Gurley impermeability is 250 sec±20 sec while the thrust strength is 6N or more.
No good: Outside the range for the above-described Good
The appearance quality of biaxially oriented sheet 14 is evaluated. To inspect appearance, LED light source having 150 lumen is employed. The upper surface of travelling biaxially oriented sheet 14 is inspected to evaluate the appearance quality. The LED light source is irradiated orthogonally to the sheet travelling direction from distance of 1 m to the film to evaluate it according to the following standards.
No good: Appearance of biaxially oriented sheet 14 travelling at the exit of lateral drawing process 5 is visually observed to distinguish light and dark.
Acceptable: Appearance of biaxially oriented sheet 14 exited from lateral drawing process 5 is cut and visually observed in a resting state to distinguish light and dark although light and dark cannot be distinguished on the travelling biaxially oriented sheet 14.
Good: Light and dark on biaxially oriented sheet 14 cannot be distinguished even in a resting state.
By comparing the Examples and Comparative Examples, we found that all Examples set the number of nip roller pairs to obtain friction force and gripping force beyond the drawing tension continuously provide microporous plastic film 11 stably with no slip and no meandering. On the other hand, all the Comparative Examples result in unacceptable slip and meandering. Accordingly, the Comparative Examples don't achieve target physical properties and mechanical properties for microporous plastic film.
Compared to Example 2, appearance quality is relatively poor in Example 1 because lubrication amount of diluent is less and dirt tends to deposit on irregularity of rough surface. Nevertheless travelling ability is stable as described above.
Compared to Comparative Example 2, the lubrication amount of diluent is less and meandering is less in Comparative Example 1. However, the gripping force in travelling direction is not enough to prevent meandering completely.
As described above, our methods make it possible to provide a microporous plastic film excellent in strength and physical properties as maintaining a travelling stability in a drawing condition where the drawing is performed to give the microporous film desirable properties.
Our microporous plastic film is applicable, but not limited in particular, to a separator used for electrochemical reaction device such as rechargeable battery, fuel cell and capacitor as well as a functional web such as filtration membrane, print film and clothing material.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2015-031389 | Feb 2015 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2016/051777 | 1/22/2016 | WO | 00 |
