JP3458924B2 - Nonwoven fabric and method for producing the same - Google Patents

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a non-woven fabric having good dimensional stability at high temperature and good heat-sealing property, and a production method for efficiently producing such non-woven fabric.

[0002]

2. Description of the Related Art Generally, a polymer having a slow crystallization rate is
There is a problem in productivity because it is difficult to perform oriented crystallization when manufacturing a nonwoven fabric by spinning and drawing processes, and it is difficult to increase the single hole discharge rate to secure dimensional stability at high temperature. It has been known. On the other hand, a polymer having a crystallization rate that is too fast has little problem in dimensional stability, but on the contrary, the heat fusion property is likely to be impaired because the crystallization progresses too much, and it is necessary to heat the polymer to the vicinity of the melting point. If the polymer having a high melting point or the polymer resin itself has a high hardness, there is a problem that the fusion processability such as calendering is not good.

Polyethylene terephthalate (hereinafter "PE
"T". ) Or polybutylene terephthalate (hereinafter referred to as “PBT”), etc., is used in various fields due to its excellent heat resistance and strength characteristics. However, in the case of PET, since the crystallization speed is slow, if the discharge amount per single hole during spinning is increased, the oriented crystallization becomes insufficient and the dry heat shrinkage ratio becomes high, resulting in a problem of dimensional stability. . In particular,
In the melt blow method, which is a means for obtaining an ultrafine fiber nonwoven fabric, it is necessary to spin the polymer in a low viscosity state at high temperature in order to make the fiber fine, and therefore it is difficult for oriented crystallization to proceed and a high temperature of 110 ° C or higher is required. It was difficult to obtain the dimensional stability at 1, and it was necessary to perform the dimensional stabilization treatment by heat treatment under tension or post-crystallization treatment by immersion in acetone. On the other hand, in the case of PBT, since the crystallization speed is fast, there is almost no problem in dimensional stability at high temperatures, and it is suitable for a spinning method such as a melt blow method, but on the contrary, crystallization proceeds too much, so that calendar processing is performed. Even if the heat-sealing treatment is carried out by the above method, there is a problem that the adhesion is not so good because the fibers are difficult to melt.

Particularly, it is difficult to bond a PET material non-woven fabric and a PBT material non-woven fabric, and it is necessary to heat the non-woven fabric to a considerably high temperature for sufficient adhesion, and there is a problem that wrinkles are generated due to shrinkage during processing. It was Further, in order to obtain a sufficient adhesive strength, the bonding processing temperature has to be raised, and there is a problem that a part is melted to form a transparent film.

As means for solving these problems, JP-A-59-223312 and JP-A-6-11648 are known.
It is conceivable to blend two or more types of polymers as disclosed in US Pat. However, in the method for producing a binder fiber disclosed in JP-A-59-223312, the process is complicated because a pre-shrinkage treatment is required, and the application to the ordinary nonwoven fabric production process is not preferable. Moreover, the purpose of the fiber is to bond, and the property is different from that of the nonwoven fabric itself as a simple structure. Further, although the adhesion is improved in the range of the mass fraction of PBT applied in the patent between 20 and 50%, increasing the single hole discharge amount causes a remarkable problem in dimensional stability at high temperature. There was a problem. Also, PBT
When the mass fraction is in the range of 50 to 60%, under normal spinning conditions, yarn breakage easily occurs, causing a problem in operability.

Further, in the method disclosed in Japanese Patent Laid-Open No. 6-116484, there is a problem that the random copolymerized polyester is used, the problem that the strength is lowered, and that the operability is lowered due to the attachment of the oligomer orifice portion or the yarn breakage. Occurred. Therefore, in the system using the random copolyester, it was necessary to carry out the two-component composite spinning as described in Examples of the patent in order to stably carry out the spinning.

Further, in Japanese Patent Laid-Open No. 4-2850, a fiber web made of PBT is disclosed, and a meltblown web having good thermal dimensional stability is also disclosed. There was a problem with the heat-sealing property (for example, calender processability, adhesiveness with other nonwoven fabrics, etc.).

In addition, recently, regarding polypropylene terephthalate (hereinafter referred to as "PPT"), spunbonded nonwoven fabrics having an average fiber diameter of 10 to 40 μm and meltblown nonwoven fabrics having an average fiber diameter of 0.5 to 10 μm are almost equivalent to PBT. It has come to be obtained under spinning conditions. However, although the elongation property is excellent, there is a problem that the strength property is insufficient.

[0009]

DISCLOSURE OF THE INVENTION According to the present invention, a non-woven fabric having good dimensional stability and adhesiveness, and particularly preferably a non-woven fabric of polyester fiber excellent in heat resistance and strength / elongation property, and the non-woven fabric are produced with high productivity. The challenge is to provide a method.

[0010]

The present invention adopts the following means in order to solve the above problems. That is, the present invention is: The first component composed of polybutylene terephthalate having a crystallization rate of 50 (1 / sec) or more in the state of supercooling degree 0.15 defined by the following formula, and the crystallization rate of 2
A second component composed of polyethylene terephthalate or polypropylene terephthalate of (1 / sec) or less,
A non-woven fabric made of long fibers having an average fiber diameter of 0.5 to 20 μm, which is made of a polymer mixed in a mixing mass ratio of 80 to 60:20 to 40, and the filling factor of the non-woven fabric is 0.05 to
A non-woven fabric having a dry heat shrinkage of 0.3 or less at a temperature corresponding to an average value of the melting point and glass transition temperature of the first component polymer of 10% or less. Supercooling degree = (equilibrium melting point−crystallization temperature) / equilibrium melting point 2. The non-woven fabric according to the first aspect, wherein the filling rate is adjusted to a range of 0.2 to 0.9 by calendar processing. 3. The nonwoven fabric according to the first or second aspect, and a crystallization rate of 2
(1 / sec) or less of polyethylene terephthalate or polypropylene terephthalate is bonded to a non-woven fabric made of fibers as a main component, and the adhesive strength is 250 g /
A laminated non-woven fabric having a length of 2 cm or more. 4. A first component composed of polybutylene terephthalate having an intrinsic viscosity of 0.4 to 1.2 and an intrinsic viscosity of 0.4 to 0.7.
Polyethylene terephthalate or intrinsic viscosity of 0.
The second component consisting of 4 to 1.0 of polypropylene terephthalate was mixed at a mixing weight ratio of 80 to 60:20 to 40, and the temperature was adjusted to 230 to 285 ° C by an extruder screw.
It is characterized in that the mixture extruded after being mixed for 0.5 to 10 minutes at a rotation speed of 5 to 30 RPM and extruded at 0.1 g / min to 3 g / min per single hole in a temperature range of 230 to 275 ° C., and then made fine. The method for producing long-fiber non-woven fabric.

[0011]

[0012]

[0013]

[0014]

[0015]

The present invention will be described in detail below. The nonwoven fabric of the present invention is preferably a long fiber nonwoven fabric produced by a spunbond method or a melt blow method, but may be a nonwoven fabric composed of short fibers. The polymer constituting the nonwoven fabric of the present invention has a first component composed of a polymer having a crystallization rate dQHv / dt of 50 (1 / sec) or more and a crystallization rate of 2 / Sec.) Or less) and a second component composed of a polymer of This aims to achieve both excellent thermal dimensional stability of a polymer having a high crystallization rate and excellent heat sealability and mutual adhesiveness of a polymer having a low crystallization rate. It is not preferable to use only a polymer having a crystallization rate of more than 2 and less than 50 from the viewpoint of stably and efficiently producing a nonwoven fabric having a good balance between dimensional stability and adhesiveness.

Since the crystallization rate depends on the polymer molecular species and molecular weight, the degree of supercooling defined by (equilibrium melting point-crystallization temperature) / equilibrium melting point is 1. Measure in the state of 5. The equilibrium melting point is
It is an extrapolated value obtained by a Hoffman-Weeks plot, and the melting point (Tm) of a sample crystallized at each isothermal crystallization temperature (Tc) was measured by DSC (differential scanning calorimeter) to find the relationship between Tc and Tm. Was plotted on a graph and the intersection of the regression line of those points and the line of Tm = Tc was taken as the equilibrium melting point. The crystallization temperature means a hot plate temperature for performing isothermal crystallization.

The crystallization rate dQHV / dt was determined by irradiating a sample with a helium-neon laser (wavelength 6328 angstrom) by means of a small angle scattering measuring device as shown in FIG. 1 when the polymer was isothermally crystallized on a hot plate. The time dependence of the scattered light intensity IHV (q) and the scattering angle θ was measured, and the scattered light intensity IHV (q) was used to investigate the time dependence of the integrated QHV by The dQHV / dt was calculated from the slope. In addition, λ is a wavelength (angstrom) and q is a conversion parameter. In FIG. 1, 1 is He-Ne.
Laser, 2 is a pinhole, 3 is a sample, 4 is an analyzer, 5 is a photodiode light receiving unit, 6 is a converter / adjuster, 7 is a processing device, and 8 is a screen.

The polymer used in the present invention is preferably polyester because of its excellent properties such as heat resistance and high elongation property. Particularly preferred polymer components include PB
It is a polymer composed of a mixed polymer of a first component composed of T and a second component composed of either PET or PPT or a mixture thereof. Here, PBT is a polyester having terephthalic acid as a main acid component and tetramethylene glycol as a main glycol component, and having a tetramethylene terephthalate unit as a main repeating unit. Further, PPT is a polyester having terephthalic acid as a main acid component and trimethylene glycol as a main glycol component, and having a trimethylene terephthalate unit as a main repeating unit. Further, PET is a polyester having terephthalic acid as a main acid component and dimethylene glycol as a main glycol component, and having a dimethylene terephthalate unit as a main repeating unit.
According to the measurement by the inventors, the crystallization rate dQHv / dt in the state where the degree of supercooling is 0.15 is PET, PPT, P
The BT was 0.4, 1.6, and 75, respectively.

The viscosity of these mixed polymers is preferably such that the difference in melt viscosity at the same temperature and the same shear rate is 50% or less of the higher viscosity value. Within the scope of the study of the present inventors, the dimensional stability of the nonwoven fabric tended to be better when the viscosity of PBT was preferably slightly higher than that of PET, but the reason is not clear.

The mixing mass ratio of the first component and the second component is 90-.
It must be between 40:10 and 60. Preferably, the mixing ratio of the first component and the second component is 80-60: 20-4.
It is desirable if it is in the range of 0, and it is more preferable that the mixing ratio is in the range of 80 to 65:20 to 35. First
When the mixing ratio of the components is more than 90%, the properties of the bulk become close to those of PBT alone, and the degree of improvement in adhesiveness is not preferable. On the other hand, when the mixing ratio is less than 40%, the state becomes close to that in which no blending is carried out, and the crystallization rate becomes too low, which is unfavorable because the thermal dimensional stability deteriorates. When the mixing ratio of the first component became less than 50%, the yarn breakage during spinning tended to start increasing,
By strictly specifying the mixing and kneading conditions in the extruder, spinning was possible to some extent. However, when the mixing ratio of the first component is less than 40%, spinning becomes difficult due to yarn breakage, and a problem occurs in operability.

The average fiber diameter is preferably between 0.5 and 20 μm. When the fiber diameter is smaller than 0.5 μm, the strength of the nonwoven fabric is reduced, which is not preferable. When the average fiber diameter is larger than 20 μm, problems such as hard texture and reduced operability occur, which is not preferable. In particular, when used as a filter, it is preferably 15 μm or less, more preferably 6 μm or less. Also,
The variation coefficient CV% of the fiber diameter is preferably 50% or less from the viewpoint of sheet uniformity, and more preferably 30.
% Or less.

The filling factor of the nonwoven fabric of the present invention is preferably in the range of 0.05 to 0.3 when used without any post-processing. When the filling rate is less than 0.05,
Probably because the number of entangled points of the fibers is reduced, there is a problem that the strength of the sheet is significantly reduced. When spinning is carried out under conditions such that a non-woven fabric having a filling factor of more than 0.3 can be obtained without post-processing, an unstable phenomenon may occur during spinning when the average fiber diameter is set between 0.5 and 20 μm. The yarn breakage is likely to occur, and particularly in the melt-blowing method, there is a problem that a fiber cut end called a shot causes a hole in the sheet to form a pinhole or a transparent film is formed, which is not preferable.

The nonwoven fabric of the present invention needs to have a dry heat shrinkage ratio of 10% or less at the average temperature of the melting point and glass transition temperature of the constituent first component polymer. In the case of polyester, it is necessary that the dry heat shrinkage ratio at around 160 ° C. is 10% or less. If the dry heat shrinkage rate is more than 10%, the sheet shrinks when the nonwoven fabric is treated with a heating flat (plain) calender or a heating embossing calender for the purpose of stacking or adjusting the filling rate, and uniform treatment becomes difficult. There are wrinkles. The dry heat shrinkage is preferably 6% or less, more preferably 3% or less. The inventor has found that as the PET content increases, the dry heat shrinkage tends to increase. Furthermore, it is also one of the preferable modes to further reduce the shrinkage rate by performing heat setting treatment by post-processing.

The non-woven fabric of the present invention (referred to as non-woven fabric A),
Nonwoven fabric B containing 50 to 100% of the second component of the nonwoven fabric
The adhesive strength was 250 when heat-bonded by an embossing roll engraved so that the fused area was 8% of the total area of the nonwoven fabric at a temperature between 70 and 220 ° C.
It is preferably g / 2 cm or more, more preferably 500 g / 2 cm or more, and particularly preferably 750 g / 2.
cm or more. The adhesive strength depends on the engraving form of the emboss, but the area of each fusion-bonded part that is pressed down is 0.1 to the diameter of a circle having the same area as the area of the pressed engraving surface (dot size). It is preferably in the range of 0.5 mm. The bonding area ratio of embossing can be variously changed, but at least 250 g / 2c with a bonding area of 8% or less.
If the adhesive strength of m can be obtained, there is no problem in use. The bonding conditions are
The appropriate value changes depending on the composition ratio of the first component and the second component of the polymer forming the nonwoven fabric A. Therefore, usually 70-2
Appropriate adhesion conditions can be determined by screening in the range of 20 ° C at intervals of 10 ° C. The fusion area ratio is preferably 3 to 40% for the purpose of stacking, and 5 to 25%.
Is more preferable.

When calendering the nonwoven fabric for the purpose of adjusting the filling rate, the filling rate is preferably between 0.2 and 0.9. Regarding the calendar treatment, from the viewpoint of the morphological stability (setting property) of the treated sheet, it is preferable that the filling rate is at least 50% or more, and more preferably 100% or more, based on the filling rate of the non-woven fabric. It is preferable to do. In the case of polyester-based non-woven fabric, the calendering temperature is 50 ° C or higher and 220
℃ or less, more preferably 80 ℃ or more 200
It is below ℃.

As a method for obtaining the nonwoven fabric of the present invention, PB having an intrinsic viscosity of 0.4 to 1.2 is used as the first component.
PE having an intrinsic viscosity of 0.4 to 0.7 as T and the second component
It is preferable to use T or PPT having an intrinsic viscosity of 0.4 to 1.0 or less.

In the present invention, the method of mixing the first component and the second component is such that the temperature of the polymer mixture is 230 ° C. or higher and 28
At a temperature of 5 ° C or less, the rotation speed of the extruder screw is 5 to
It is necessary to mix for 0.5 to 10 minutes at 30 RPM and then extrude. Extrusion temperature, rotation speed and residence time are in a range of conditions in which polymer viscosity does not fluctuate significantly due to molecular cleavage due to shearing or exchange reaction of ester bond, etc. Within the range of the present invention, the higher rotation speed and the shorter residence time are particularly preferable. With respect to the screw rotation speed, if the rotation speed is higher than 30 RPM, a decrease in viscosity, which is considered to be caused by a transesterification reaction or molecular chain breakage due to shearing, becomes remarkable, and spinning becomes unstable. Rotation speed is 5R
If it is smaller than PM, the mixing becomes insufficient, and the viewpoint of stabilizing the spinning and the unevenness of thermal dimensional stabilization occur, which is not preferable. The melt residence time of the polymer is preferably set to 0.5 to 10 minutes, and preferably 0.5 to 5 minutes. As one of the most preferable forms of the mixing method, it is also preferable that the mixing is carried out uniformly by a twin-screw extruder in the shortest possible time.
Alternatively, the mixture may be kneaded in advance with a twin-screw extruder or the like and then pelletized, and the pellets may be extruded with a normal single-screw extruder. Depending on the case, you may use the polymer which copolymerized the polymer of the said composition previously.

As one of the desirable modes of the method for producing the nonwoven fabric of the present invention, in a spunbond method or melt blow method extruder, the extrusion temperature of the mixture extruded by the extruder is set to a temperature range of 230 ° C. to 275 ° C. It is preferable to set the pore size, extrude at a rate of 0.1 g / min or more and 3.0 g / min or less per single hole, and then make it thin. If the discharge rate is less than 0.1 g / min per single hole, the residence time in the heating pipe becomes longer and the heat deterioration or the transesterification reaction is likely to proceed. Operability deteriorates. On the other hand, even with a discharge rate of more than 3.0 g / min, spinning becomes unstable and yarn breakage easily occurs, and there is a problem in dimensional stability of the nonwoven fabric at high temperatures.
Particularly, in the melt-blowing method which is advantageous for the production of ultrafine fibers, the air temperature after melt extrusion is 0.1 g / min or more and 1.0 g / min or less per single hole. It is preferable to pull and elongate the polymer. If the polymer discharge temperature exceeds 275 ° C., the dry heat shrinkage ratio becomes high, and if it is less than 230 ° C., yarn breakage is likely to occur, which is not preferable.

[0030]

BEST MODE FOR CARRYING OUT THE INVENTION As one of the most preferable embodiments of the present invention, there is a case where the material of the non-woven fabric or laminated sheet is a polyester polymer. For example, a sheet material such as a spunbonded non-woven fabric or a film made of PET and the non-woven fabric of the present invention are laminated 70 to 2
It is one of the preferable forms to be fused and integrated by an embossing calender roll in a temperature range between 20 ° C.
In particular, when the nonwoven fabric of the present invention is a nonwoven fabric obtained by the melt blow method, the strength tends to be small,
Reinforcement by lamination with a spunbond nonwoven fabric or a film is particularly preferable.

[0031]

EXAMPLES The following examples are intended to clarify the present invention, but the present invention is not limited thereto.
Each physical property value in the examples was measured by the following methods. I. Temperature at 4 to 5 points from the equilibrium melting point of 190 ° C to the melting point of each polymer (T
The sample crystallized isothermally in c) was subjected to melting point (Tm) measurement by DSC, and the intersection of the regression line and the Tc = Tm line was taken as the equilibrium melting point.

B. Crystallization rate The crystallization rate at a supercooling degree of 1.5 was determined by the small-angle light scattering apparatus shown in FIG. That is, He-N
An e (helium-neon) laser was irradiated to measure the time dependence of the scattered light intensity IHV (q) and the scattering angle θ of the scattered light, and the integrated value QHV of the scattered light intensity with respect to q was obtained. The crystallization rate dQHV / dt was determined on the assumption that this QHV is proportional to the volume fraction of the crystal. When the absolute value varies depending on the measuring device, the crystallization rate of PBT resin (N-1500 manufactured by Mitsubishi Rayon Co., Ltd.) having an intrinsic viscosity of 0.58 is used as a reference,
It suffices to determine the proportional constant so that the value becomes 75 and perform proportional conversion. Here, q is a conversion parameter and is calculated by the following formula. q = (4π / λ) sin (θ / 2) In addition, t represents time and λ represents wavelength.

C. Into 25 ml of a solution in which the intrinsic viscosity of parachlorophenol and tetrachloroethane were mixed in a mass ratio of 3: 1, the dry polymer was added to 0.2 ml.
It melt | dissolved 1g, it put into the Ubbelose viscous tube, the fall velocity in the temperature of 30 degreeC was measured, and it determined using the Huggins formula. For simplification, also for PPT and PBT, the conversion formula of the intrinsic viscosity from the relative viscosity was calculated using the same formula as that of PET.

D. From the enlarged photograph of the average fiber diameter 2000 times (scanning electron microscope), 50
The fiber diameter of 0 fibers was read with a caliper, and the arithmetic average was taken as the average fiber diameter. E. The thickness of the non-woven fabric was measured under a load of 7 g / cm ² , and the volume filling rate, which is a value obtained by dividing the basis weight by the product of the thickness and the polymer density, was adopted.

F. Dry heat shrinkage A square sheet having a side of 16 cm was cut out, heat-treated in an oven at an average temperature of the melting point of the first component polymer and the glass transition temperature for 15 minutes, and then calculated from the rate of change of the sum of the four sides. .

G. Adhesive strength A laminated sheet was cut into a rectangle with a sample length of 10 cm and a width of 2 cm, the adhesive surface was manually peeled off by a length of 5 cm, and the peeled portion was placed either above or below so that the gripping length would be 5 cm. The maximum tension until the two non-woven fabrics are completely peeled off by finding the relationship between the tension and strain when sandwiched in a chuck and set in a tensile strength measuring machine and conducting a tensile test at 5 cm / min. Was defined as the adhesive strength.

H. A sheet with liquid filter performance of 40 g / m ² was hollowed out to a diameter of 47 mm, and 5
After stacking the sheets and placing them in a holder, a filtration test was performed at a linear velocity of 5 cm / min and an effective filtration area of 13.8 cm ² by using ion-exchanged water in which 100 PPM of 0.6 μm alumina particles were dispersed. The initial filtration accuracy was calculated from [(inlet concentration-outlet concentration) / inlet concentration] × 100 using the inlet concentration and the outlet concentration at the time when the outlet concentration became the maximum. The concentration was measured using a Mitsubishi Kasei Poic densitometer.

Examples 1 and 2, Reference Example 1 PBT manufactured by Mitsubishi Rayon Co., Ltd. (product name: N-1500,
By changing the mixing mass of the limiting viscosity 0.58) and the PET manufactured by Toyobo Co., Ltd. (product name: RE530, limiting viscosity 0.62), the temperature of the polymer mixture is 275 ° C., and the rotation speed of the extruder screw is 25 RPM. The mixture extruded after mixing for 3 minutes between
0.5g / per hole in the temperature range from 0 to 270 ℃
Melt blown spinning was performed by extrusion in minutes. The spinning conditions were adjusted so that the average fiber diameter was between 2 and 3 μm. The obtained non-woven fabric had a small dry heat shrinkage, and even when heat was applied in the post-processing, the dimensional change was small and there was no problem. Also, in order to check the laminating processability of nonwoven fabric, PE manufactured by Toyobo Co., Ltd.
T-spun bond nonwoven fabric (Product name: 6601A) and 160 ° C
Embossing was carried out. All adhesive strengths were sufficient and no peeling occurred. Details are shown in Table 1.

Comparative Examples 1 to 3 PBT manufactured by Mitsubishi Rayon Co., Ltd. (product name: N-1500,
The blending mass ratio of the limiting viscosity 0.58) and PET manufactured by Toyobo Co., Ltd. (product name: RE530, limiting viscosity 0.62) was changed as shown in the attached table, and the temperature of the polymer mixture was adjusted to 280.
The mixture was extruded after mixing for 3 minutes at a rotation speed of the extruder screw of 25 RPM at 0 ° C., and the temperature of the polymer mixture was 0.5 g / min per hole in the temperature range of 250 ° C. to 285 ° C. Melt blown spinning was carried out by extrusion. The spinning conditions were adjusted so that the average fiber diameter was between 2 and 3 μm. The non-woven fabrics of Comparative Examples 2 and 3 had a high dry heat shrinkage rate, and when heat was applied in the post-processing, non-uniform wrinkles were generated, and there was a problem in the post-processing passability. On the other hand, the non-woven fabric of Comparative Example 1 was attempted to adhere to the PET spunbonded non-woven fabric, but it was not adhered at 160 ° C. at all. 225 ° C
Although the calendar roller was heated up to, the adhesive strength was low, and the joint surface could be easily peeled off by hand, and the adhesion was insufficient. At this time, there also occurred a problem that a part of the laminated sheet was melted and made transparent. Details are shown in Table 1.

Example 3 PBT having an intrinsic viscosity of 0.58 and PBT having an intrinsic viscosity of 0.75
PT was mixed at a mixing mass ratio of 60:40, the temperature of the polymer mixture was 275 ° C., and the mixture was extruded for 3 minutes while the extruder screw rotation speed was 25 RPM. Was extruded at 260 ° C. at a rate of 0.5 g / min per single hole to perform melt blown spinning. The dry heat shrinkage was 3.2%, and the lamination adhesiveness with PET spunbond was also good. Details are shown in Table 1.

[0041]

[Table 1]

Reference Example 2 The non-woven fabric of Reference Example 1 was smoothed with a plain resin calender at a roll temperature of 160 ° C., a linear pressure of 25 Kg / cm and a flow rate of 20 m / min. The sheet was good with little fuzz.

Comparative Example 4 The non-woven fabric of Comparative Example 1 was smoothed with a plain resin calender at a roll temperature of 160 ° C., a linear pressure of 25 kg / cm and a flow rate of 20 m / min. Rubbing the sheet with fingers caused fuzz. When the sheet was bent, the thickness of that portion returned and became thick, and the calendering workability was insufficient.

[0044]

The non-woven fabric satisfying the requirements of the present invention has good dimensional stability and adhesiveness and is therefore suitable as a non-woven fabric to be used as a filter material or laminated. Especially when the non-woven fabric of the present invention is composed of polyester, the non-woven fabric and its laminate having particularly excellent properties such as hydrophilicity, heat resistance, and strength / elongation properties can be produced at relatively low cost. It becomes possible to supply well, and it is possible to supply a non-woven fabric suitable for a filter, a non-woven fabric for clothing, a non-woven fabric for medical use and the like. Further, the post-processability is remarkably suitable due to the excellent dimensional stability and adhesiveness of the nonwoven fabric.

By applying the production method of the present invention, it becomes possible to efficiently produce a non-woven fabric having good dimensional stability and good heat-sealing property and heat-bonding property.

[Brief description of drawings]

FIG. 1 is a block diagram of a scattered light intensity measuring device.

[Explanation of symbols]

1 He-Ne laser 2 pinholes 3 samples 4 analyzer 5 Photodiode receiving unit 6 Conversion / adjustment unit 7 processor 8 display screen

Claims (4)

(57) [Claims] 1. A degree of supercooling defined by the following formula: 0.15
Poly crystallization rate in the state of more than 50 (1 / sec)
First component consisting of butylene terephthalate and polyethylene terephthalate having a crystallization rate of 2 (1 / sec) or less
Or polypropylene terephthalate - and a second component consisting of bets, weight ratio 80 to 60: - long average fiber diameter consisting of 0.5~20μm mixed polymer with 20 to 40
A non-woven fabric made of fibers and having a filling factor of 0.
In 05 to 0.3, the first component polymer - nonwoven dry heat shrinkage at a temperature corresponding to the average value of the melting point and glass transition temperature, characterized in Oh Rukoto 10% or less. Supercooling degree = (equilibrium melting point-crystallization temperature) / equilibrium melting point 2. A filling rate of 0.2 to 10 by calendering.
The non-woven fabric according to claim 1, adjusted to a range of 0.9. 3. The non-woven fabric according to claim 1 or 2, and a crystallization speed.
Polyethylene terephthalate less than 2 (1 / sec)
Fibers mainly composed of polypropylene terephthalate
Adhesive strength of 25
A laminated non-woven fabric characterized by having a weight of 0 g / 2 cm or more. 4. A first component comprising polybutylene terephthalate having an intrinsic viscosity of 0.4 to 1.2 and an intrinsic viscosity of 0.4.
0.7 Polyethylene terephthalate of - DOO or intrinsic viscosity 0.4 to 1.0 polypropylene terephthalate - or bets
Ranaru the second component, the mixing weight ratio 80 to 60: 20 to 40
And the temperature is adjusted to 230 to 2 by an extruder screw.
The mixture extruded after mixing for 0.5 to 10 minutes at 85 ° C. and a rotation speed of 5 to 30 RPM was extruded in the temperature range of 230 to 275 ° C. at 0.1 g / min to 3 g / min per single hole, and then finely divided. A method for producing a long fiber non-woven fabric, which is characterized by the following.