KR20150114031A - Anionic copolyesters/sodiumdodecylbenzensulfonate blend films, nanofilament and method for preparing of the same - Google Patents

Abstract

The present invention relates to a blend film which provides improved caustic reductivity by comprising anionic copolyester and sodium dodecylbenzenesulfonate, a nanofilament, and a manufacturing method thereof.

Description

TECHNICAL FIELD The present invention relates to an anionic copolymerized polyester / sodium dodecylbenzenesulfonate blend film, an anionic copolymerized polyester / sodium dodecylbenzenesulfonate blend film, a nanofilament and a method for producing the same,

The present invention relates to blend films, nanofilaments comprising anionic copolymerized polyester and sodium dodecylbenzenesulfonate and a process for their preparation.

The nanofilaments are ultrafine filaments having a cross-sectional diameter ranging from several hundreds to several tens of nanometers. In general, the sea-island hybrid radiation method is most advantageous in producing nanofilaments having uniform thickness and sufficient strength.

The production of nanofilament of sea-island complex radial type is also important for the design of hardware and process control such as spinning and detaching, but also the rapid dissolution of marine polymer and the uniform division of isoelectric fiber is one of important process factors. Particularly, when nanofilaments having a nanometer-scale diameter are manufactured using sea-island composite radiation, as the final single-filament fineness decreases, the number of degrees of insertion per unit area and thus the specific surface area increase sharply, The penetration of the alkali becomes difficult and the leaching of the sea component polymer is adversely affected.

In addition, when the alkaline hydrolysis or reduction is proceeded under more severe conditions for the rapid elution of the sea component polymer, the conductive fiber bundle is also invaded at the same time, which makes it difficult to produce a uniform fiber.

Therefore, in the production of nanofilaments, it is necessary to design and manufacture a marine polymer having faster dissolution characteristics.

Conventionally, marine polymeric polymers used in sea-island composite spinning and microfiber fabrication generally include dimethyl 5-sodiumsulfo isophthalate (DMS), poly (ethylene glycol), PEG, Is an anionic copolyester introduced into the main chain of the polyester. However, the method of increasing the content of these copolymers in order to improve the elution properties causes a decrease in the molecular weight due to high melt viscosity, a drop in the melting point, a decrease in the crystallization rate, or a phenomenon in which the melting point disappears and only the softening point is present. The fiber formation becomes difficult and the physical properties of the spun yarn become weak, which may cause various problems in the post-treatment process.

Therefore, it is not preferable to use an excess amount of a comonomer for improving the dissolution rate of anionic copolymerized polyester. A new approach that can selectively improve only the alkali reduction characteristic while maintaining the thermal properties of these materials, Method is needed.

On the other hand, it is well known that fibers melt-spun at high speed have molecular orientation degree and crystallinity higher than a certain level. The anionic copolyester, which is a marine polymer used for producing nanofilaments, is no exception, and the degree of molecular orientation is determined and the degree of crystallization is determined in the spinning and post-drawing processes. However, it is very difficult to evaluate or predict various microstructures of the anionic copolyester in the radiated state, since it is practically very difficult to physically separate the radiating and segregating components. In addition, since the radiated raw yarn is produced in the form of a fabric such as a woven / knitted fabric, a nonwoven fabric and the like, and most of these copolyesters are removed through alkali reduction treatment, evaluation of the microstructure of the copolymerized polyester after spinning gives a great meaning no. However, since the crystallinity determined in the spinning step may affect the alkali reduction characteristics in the final yarn and fabric state, the interpretation of the correlation between the crystallinity and the alkali reduction characteristic of the conventionally used anionic copolymer polyester It is very important. When the nanofilaments are produced by using the anionic copolymer polyester having the same composition as the sea component, the degree of crystallization of the copolymerized polyester is determined by the spinning temperature condition, the post-drawing process and the subsequent change in thermal history, Can be affected.

In addition, since most of the literature including the above-mentioned prior art studies evaluates the alkali loss characteristics of anionic copolymerized polyester mainly by using an amorphous film or a dried chip, these results show that in the state of actual yarn in which a certain degree of crystallinity is expressed Of the dissolution profile of the drug. In particular, when the low-molecular weight compound such as DBS is present in the fiber matrix, the alkali-reducing property can be directly influenced by the crystallinity of the matrix. Therefore, the effect of introducing DBS in an amorphous film or a simple- It does not systematically compare or identify phenomena.

 Do Sung Joon, Baek Doo Hyun, "Nanofilament Manufacturing Technology", Textile Technology and Industry, 2010, 14, 47-54.  KJ Hsiao, JL Kuo, JW Tang, and LT Chen "Physicochemical and Kinetic Properties of Alkaline Hydrolysis of Cationic Dyeable Poly (ethylene terephthalate) and Polyethylene Glycol (PEG) -Modified CDPET Polymers: Effects of Dimethyl 5-Sulfoisophthalate Sodium Salt / PEG Content and the Number-Average Molecular Weight of the PEG ", Polymer Science, 2005, 98, 550-556.  ZY Oian, S. Li, Y. He and XB Liu, "Synthesis and in vitro degradation study of poly (ethylene terephthalate) / poly (ethylene glycol) (PET / PEG) multiblock copolymer", Polymer Degradation and Stability, 83, 93-100.  O. Gaona, D. P. R. Kint, A. M. de Ilarduya, A. Alla, J. Bou, S. Munoz-Guerra "Preparation and hydrolytic degradation of sulfonated poly (ethylene terephthalate) copolymers", Polymer. 2003, 44, 7281-7289.  Y. J. Kim, M. H. Jee, E. H. Lee, J. U. Choi, D.H. Noh, H.K. Rho, and D.H. Baik, "Effects on Molecular Weight of Poly (ethylene glycol) on the Thermal Properties and Alkaline Hydrolysis of Copolyesters", Tex. Sci. Eng., 2012, 49 (1), 1-8. H. I. Kim, C. H. Jeong, and M. H. Min, "Accelerating Effects of Organic Acid Treatment on Weight Reduction Characteristics of Sea-Island Type PET Supermicrofiber (1)", Tex. Col. Finsh., 2012, 24 (1), 45-53.  E. S. Shin, H. S. Kim, and J. J. Lee, "Weight Reduction Behavior and Dyeing Properties of Sea-island PET Ultra-microfiber Knitted Fabrics ", Tex. Sci. Eng., 2012, 49 (1), 18-25.  S. J. Choi, N. K. Ye, M. H. Min, and H. S. Kim, "Optical Properties of Nanofilament Fabrics", Tex. Sci. Eng., 2013, 50 (2), 96-101.  Y. Li, and C. W. Joo, "Structural Factors and Physical Properties of Needle-punched Nonwovens Based on Co-PET / PA Bicomponent Fibers via Alkali Treatment", Fibers and Polymers, 2012, 13 (4), 456-465.  W. Zhang, D. Shen, "The Effects of Thermal Histories on Crystallization of Poly (ethylene terephthalate) ", Polymer Journal, 1998, 30 (4), 311-314.  Z. Chen, J. N. Hay, M.J. Jenkins, "Thermal Analysis of Poly (ethylene terephthalate) by FTIR Spectroscopy", Thermochimica Acta, 2013, 552, 123-130.  M. Bertoldo, M. Labardi, C. Rotella, S. Capaccioli, "Enhanced Crystallization Kinetics in Poly (ethylene terephthalate) Thin Films Evidenced by Infrared Spectroscopy", Polymer, 2010, 51, 3660-3668.  J. S. Jang, J. H. Oh, and S. I. Moon, "Crystallization Behavior of Poly (ethylene terephthalate) Blends with Hyperbranched Polymers: The Effect of Terminal Groups and Composition of Hyperbranched Polymers", Macromolecules, 2000, 33, 1864-1870.  Y. Zhang, Y. Lu, Y. Duan, J. Zhang, S. Yan, and D. Shen, "Reflection-Absorption Infrared Spectroscopy Investigation of Crystallization Kinetics of Poly (ethylene terephthalate) Ultrathin Films", J. Pol. Sci: Part B: Pol. Phys., 2004, 42, 4440-4447.  Y. Zhang, J. Zhang, Y. Lu, Y. Duan, S. Yan, and D. Shen, "Glass Transition Temperature Determination of Poly (ethylene terephthalate) Thin Films Using Reflection-Absorption FTIR", Macromolecules, 2004, 37 , 2532-2537.  J. R. Atkinson, F. Biddlestone, J. N. Hay, "An Investigation of Glass Formation and Physical Aging in Poly (ethylene terephthalate) by FT-IR Spectroscopy", Polymer, 2000, 41, 6965-6968.

An object of the present invention is to provide a blend film, a nanofilament and a method for producing the same, which are excellent in alkali weight loss property by mixing an anionic copolymer polyester and sodium dodecylbenzenesulfonate.

In order to accomplish the above object, the present invention provides a blend film comprising an anionic copolymerized polyester and sodium dodecylbenzenesulfonate.

The content of the sodium dodecylbenzenesulfonate is preferably 1 to 10% by weight based on 100% by weight of the total blend film.

The thickness of the blend film is preferably from 10 탆 to 100 탆.

The blend film is characterized in that the time required for 100% reduction of alkali in an aqueous solution of 1.0 wt% of NaOH at 98 캜 is 20 minutes or less.

The present invention also provides a nanofilament comprising an anionic copolymerized polyester and sodium dodecylbenzenesulfonate.

Here, the nano filament is a sea type.

In addition, the present invention provides a method for producing a thermoplastic resin composition, which comprises melt-extruding an anionic copolymerized polyester and sodium dodecylbenzenesulfonate by mixing; Quenching the extruded mixture, cutting into chips and vacuum drying; And pressing the dried chip with a hot press. The present invention also provides a method for producing a blend film.

The blend film and the nano filament according to the present invention include sodium dodecylbenzenesulfonate based on anionic copolymerized polyester, so that the alkali loss-reducing property can be improved while maintaining the thermal property as much as possible. Therefore, such a blend film has an improved dissolution rate of the anionic copolymerized polyester, so that it is easy to produce sea-island nano filaments.

Fig. 1 is a graph showing the evaluation results of a film according to Example 1 at 98 占 폚, a 1.0 wt% NaOH aqueous solution, a chip according to Comparative Example 1, and a 100% weight loss time of an alkali yarn according to Comparative Example 2;
FIG. 2 is a graph showing the evaluation of a 100% reduction in alkali time according to the heat treatment time of the film according to Example 1. FIG.
FIG. 3 shows the FT-IR spectrum of the film of Example 1 which was heat-treated at 15 ° C and 140 ° C for 30 minutes, respectively.
4 shows the results of evaluation of the glass transition temperature of the film according to Example 1 by FT-IR.
5 is a graph showing a change in fraction of Trans according to Examples 1 to 6 over time at a temperature condition of 100 캜.
6 is a graph showing the 100% alkali reduction time and trans fraction of the film according to Examples 1 to 6. Fig.
7 is a graph showing a 100% reduction in alkali time of the film according to Examples 1 to 6;

Hereinafter, the present invention will be described in detail.

The present invention provides a blend film comprising an anionic copolymerized polyester and sodium dodecylbenzenesulfonate (DBS).

Here, the content of the sodium dodecylbenzenesulfonate is preferably 1 to 10% by weight based on the total weight of the blend film, but is not limited thereto.

When the content of sodium dodecylbenzenesulfonate is in the above range, excellent alkali reducing properties can be obtained.

Since such a blend film has the dissolution characteristics of a rapid anionic copolymerized polyester, it can be easily applied to the production of nano-scale nano filaments.

Accordingly, the present invention also provides nanofilaments comprising anionic copolymerized polyester and sodium decylbenzenesulfonate. At this time, the content of sodium dodecylbenzenesulfonate is preferably 1 to 10% by weight based on the total weight of the nano filament.

Further, the nano filament is characterized by being a sea type.

The method for preparing the blend film comprising the anionic copolymer polyester and the sodium dodecylbenzenesulfonate according to the present invention is not particularly limited, but can be produced through the following process.

First, the anionic copolymerized polyester and sodium dodecylbenzenesulfonate are mixed and melt-extruded. In this case, a twin-screw extruder is preferably used, and the melting temperature is not particularly limited, but is preferably 220 to 250 ° C.

Thereafter, the extruded stranded mixture is quenched in ice water, cut into chips and vacuum dried. Vacuum drying is preferably performed at a temperature of 80 DEG C for 24 hours, but is not limited thereto.

The dried chips are compressed by using a hot press, and then quenched into ice water to obtain a blend film. Here, the temperature of the pressing process is not particularly limited, but it is preferable that the temperature is 250 to 300 캜.

The thickness of the blend film produced by the above method is preferably 10 탆 to 100 탆, but is not limited thereto.

Further, the blend film of the present invention is characterized in that the time required for 100% reduction of alkali in an aqueous solution of 1.0 wt% of NaOH at 98 占 폚 is 20 minutes or less, thereby improving the alkali reducing property.

In the present invention, the anion type copolymerized polyester and DBS were melted and mixed in various concentration ranges to prepare an amorphous film, and the thermal properties and the alkali reduction characteristics of these films were systematically analyzed. In order to confirm the correlation between the crystallinity of the anionic copolymerized polyester and the alkali reduction characteristic, the alkali anion reduction was carried out after the stepwise heat treatment of the pure anionic copolymer polyester without DBS. Based on the result, DBS The samples were also heat treated to have similar crystallinity above a certain level, not amorphous films, and the alkali loss characteristics were evaluated. In addition, relative comparison of the degree of crystallization according to the heat treatment of all the samples was carried out by using an infrared spectroscopy (Fourier transform infrared spectroscopy).

On the other hand, in order to effectively evaluate the alkali-reduction characteristics by introducing DBS, it is necessary to exclude the parameter due to the crystallization difference between the samples, unless it is in the state of an amorphous film. However, in general, the crystallization behavior of polymer in DBS is likely to be regarded as an external foreign substance. Therefore, the crystallization degree of DBS in all samples subjected to the same heat treatment condition may be influenced by the DBS content. Therefore, it is most preferable to present the heat treatment conditions for each sample so that the degree of crystallization of all the samples may show a similar level.

In general, thermal properties such as melting point and crystallinity of a polymer material can be evaluated by using differential scanning calorimetry (DSC) or FT-IR. Among them, spectroscopic analysis of a polymer using FT-IR can be carried out by measuring the stereostructure of a polymer, It is well known that it provides relatively fast and accurate information about interaction. Particularly, in the case of polyethyleneterephthalate (PET), the characteristic bands of 1340 and 1370 cm ^-1 , which correspond to the wagging modes of the ethylene glycol repeating units, are represented by the trans- and asymmetric (Gauche) , And various studies have been made on the glass transition temperature, crystallization degree and crystallization kinetics of PET using these two characteristic bands. In the case of the anionic copolymer polyester used in the present invention, since the formation of crystals is closely related to these two characteristic bands, the evaluation of the crystallinity and the presentation of the heat treatment conditions for each sample are made by comparing the relative crystallinity with FT-IR . However, unlike pure PET, the copolymerized polyester used in the present invention has a structure in which PEG is copolymerized in the main chain. Therefore, the result obtained through FT-IR does not reflect actual crystallinity, And the relative comparison between the samples is possible.

Hereinafter, the present invention will be described in detail with reference to examples. However, these examples are for illustrating the present invention specifically, and the scope of the present invention is not limited to these examples.

[material]

Sodium dodecylbenzenesulfonate (DBS, technical grade) and NaOH (98.0%) were purchased from Sigma-Aldrich and Samchun Chemical, Korea, respectively, and used without further purification .

Anionic copolymerized polyesters are based on poly (ethylene terephthalate) (poly (ethylene terephthalate)) and include dimethyl 5-sodumsulfo isophthalate (DMS) and poly (ethylene glycol) , PEG) as a comonomer was used as a chip. The content of the dimethyl 5-sodium sulfoisophthalate was 1 to 10 mol% based on the total molar amount, and the poly (ethylene glycol) But it is not limited thereto.

[Example 1] Production of an anion type copolymerized polyester amorphous film

An anionic copolymerized polyester was melt-extruded at a temperature of 220 to 250 DEG C by using an extruder. The extruded stranded mixture was quenched in ice water, cut into chips and vacuum dried at a temperature of 80 DEG C for 24 hours. Thereafter, the dried chips were compressed at a temperature of 260 ° C for 5 minutes using a hot-press, and then quenched into ice water to prepare an amorphous film having a thickness of about 100 μm.

[Example 2] Preparation of an anion-type copolymerized polyester / Dodecylbenzenesulfonate blend amorphous film

Anion type copolymerized polyester and 1 wt% of dodecylbenzenesulfonate (DBS) were melt-extruded at a temperature of 220 to 250 ° C using a twin-screw extruder (BK-11, Bautek, Korea). The extruded stranded mixture was quenched in ice water, cut into chips and vacuum dried at a temperature of 80 DEG C for 24 hours. Thereafter, the dried chips were compressed at a temperature of 260 ° C for 5 minutes using a hot-press, and then quenched into ice water to prepare an amorphous film having a thickness of about 100 μm.

[Examples 3 to 6] Preparation of an anion type copolymerized polyester / sodium dodecylbenzenesulfonate blend amorphous film

An amorphous film was prepared in the same manner as in Example 1, except that the sodium dodecylbenzenesulfonate (DBS) content was 3 wt%, 5 wt%, 7 wt%, and 10 wt%, respectively.

[Comparative Example 1] Anionic copolymerized polyester chips

Anionic copolymerized polyesters are based on poly (ethylene terephthalate) (poly (ethylene terephthalate)) and include dimethyl 5-sodumsulfo isophthalate (DMS) and poly (ethylene glycol) , PEG) was introduced as a comonomer was used as a chip state.

[Comparative Example 2] A 600 nm-grade nano filament yarn

The 600 nm-grade nano filament yarn was prepared by using the chip used in Comparative Example 1 as a sea component in a sea-island composite spinning (sea water ratio 4: 6).

[Experimental Example]

The alkali reduction was carried out in an aqueous solution of 1.0 wt% of NaOH at 98 ° C, and the time point at which the transparent solution state began to be visible to the naked eye was regarded as 100% reduction, and the time was recorded to evaluate the weight loss characteristics. Further, in order to reduce the deviation of the alkali weight loss characteristic due to the difference in the surface area of the film, all the samples were cut into a uniform size of 5 mm in width and 5 mm in length. Finally, relative comparisons of crystallizations due to heat treatment were analyzed using an infrared spectrometer (Fourier transform infrared spectroscopy, Nicolet iS500 FT-IR, Thermo Scientific).

[Experimental Example 1] Evaluation of alkali weight loss characteristics

The anion type copolymerized polyester may have an influence on the elution characteristics in the final yarn or fabric state depending on the degree of crystallization. In order to confirm this, the alkali weight loss characteristics of the amorphous film prepared in Example 1, the chip prepared in Comparative Example 1 and the 600 nm nano filament yarn prepared in Comparative Example 2 were evaluated.

The weight loss of alkali was measured at 98 ° C in aqueous solution of 1.0 wt% of NaOH. The time point at which the sample began to become transparent to the extent that the sample could not be seen visually was regarded as 100% The results are shown in Fig. At this time, in order to reduce the deviation of the alkali weight loss characteristic due to the difference in the surface area of the film, all the samples were cut into a uniform size of 5 mm in width and 5 mm in length.

As can be seen from FIG. 1, the amorphous film (Example 1) had a time of 18 minutes only in the case of 600 nm nano-filament yarn (Comparative Example 2) It was confirmed that the 100% reduction was completed. In addition, it was observed that the time taken for the dried chip (Comparative Example 1) to attain a 100% reduction amounted to 242 minutes. As a result, it was confirmed that there was a large difference in the behavior of alkali reduction according to the state of the sample.

In the case of the amorphous film (Example 1), since the crystallization degree is expected to be lower than that in the yarn state, the time for reaching the 100% loss can be short. However, in the case of chips, the surface crystallization and the increase in total crystallinity, It is judged that the weight loss is delayed. Therefore, it is considered that it is most preferable to evaluate the alkali weight loss property of the anionic copolymerized polyester by inducing crystallization through an appropriate heat treatment of the amorphous film and evaluating the alkali loss weight property accordingly.

[Experimental Example 2] Alkali weight loss characteristics according to heat treatment time

The alkali reduction characteristics of the amorphous film prepared in Example 1 according to the heat treatment time at a temperature of 100 캜 were evaluated in the same manner as in Experimental Example 1. The results are shown in Fig.

As can be seen from FIG. 2, the time required for 100% reduction rapidly increases with the increase of the time in the initial stage of the heat treatment, and it is observed that the slope of the curve becomes gentle while the heat treatment time exceeds 80 minutes. These results indicate that the crystallization degree of the amorphous film is increased by the heat treatment, and the alkali reduction characteristic of the copolymer polyester is remarkably lowered due to the increased crystallinity.

[Experimental Example 3] Thermal characteristic analysis

The amorphous film prepared in Example 1 was subjected to a heat treatment for 30 minutes at a temperature of 15 ° C (dotted line) and 140 ° C (solid line), and then FT-IR (Fourier transform) was performed using Nicolet iS500 FT-IR (Thermo Scientific) infrared spectroscopy analysis. The results are shown in FIG.

As can be seen in Figure 3, the spectrum commonly Trans and Gauche and shows a characteristic band of 1340 and 1370cm ^-1 corresponding to the three-dimensional shape, according to the heat treatment whether or not the strength of 1340 cm ^-1 is increased significantly, and 1370 cm ^{- 1} was relatively decreased. In other words, the characteristic band of 1340 and 1370 cm ^-1 can be considered to be very sensitive to heat treatment and conformational change of the molecular chain. By using the intensity or area of the two characteristic bands, as shown in FIG. 4, Is also possible.

FIG. 4 shows the result of FT-IR evaluation of the glass transition temperature of the amorphous film prepared in Example 1. For comparative comparison, DSC analysis results of the same sample were inserted.

As can be seen from FIG. 4, the glass transition temperature of the copolymerized polyester analyzed by FT-IR was about 71.7 ° C, which was slightly different from that measured by DSC at 66.8 ° C, but comparable results were obtained .

[Experimental Example 4] Trans fractional change evaluation

For comparison of the isothermal crystallization behavior of the amorphous films prepared in Examples 1 to 6, the trans fractional change with time was evaluated at a temperature of 100 ° C, .

At this time, the fraction of Trans is generally used to predict information on the crystal phase of PET, and A and k represent the area value and the absorption coefficient in the respective characteristic bands, respectively. As can be seen from FIG. 4, the change of the trans fraction according to the heat treatment time is very similar to the DSC isothermal crystallization curve of a general crystalline or semi-crystalline polymer, and the behavior of the Trans fraction changes with increasing DBS content . In addition, in the case of the films in which 1 wt% and 3 wt% of DBS were added (Examples 2 and 3), the rate of increase of the Trans fraction was slower than that of the pure copolymer (Example 1) In the films (Examples 4 to 6) added with 5 wt%, 7 wt% and 10 wt%, respectively, the rate of increase of the trans fraction at the initial stage of the heat treatment was considerably slow and the value at the final time was also lowered in accordance with the increase of DBS content there was. That is, based on the results shown in FIG. 5, it can be expected that the introduction and content of DBS significantly affect the crystallization behavior of the copolymerized polyester and delay the crystallization and crystallization rate.

[Experimental Example 5] Assessment of alkali loss by introduction of DBS

Based on the results of FIGS. 2 and 5, the treatment time of each amorphous film prepared in each of Examples 1 to 6 at a temperature of 100 ° C. was measured in order to investigate the effect of DBS introduction on the alkali reduction of anionic copolymerized polyester The heat treatment was carried out differently and the weight loss characteristics of the film were evaluated.

At this time, since the influence of the difference in crystallinity should be excluded regardless of whether or not DBS is introduced, the heat treatment conditions of each amorphous film should be carefully selected and the method is as follows. First, in the case of the 600 nm class yarn (Comparative Example 2), about 45 minutes to 100% of the weight loss was obtained. From the result of the heat treatment time and the loss time of FIG. 2, the appropriate heat treatment time of the copolymerized polyester was derived. The heat treatment time was substituted into the result of FIG. 5, and information about the heat treatment conditions (100 ° C., 28 minutes) and the crystallinity (14,2%, Trans) were obtained at about 45 minutes. Thereafter, based on the results of FIG. 5, heat treatment time was obtained in which the Trans content of the DBS-containing films was 14.2%.

As a result, the heat treatment time of each film at 100 ° C was from 24 minutes to 73 minutes at the minimum, and the Trans fraction, which is a characteristic related to crystallization of each film due to the heat treatment, is shown in FIG.

In addition, the films prepared in Examples 1 to 6 were subjected to heat treatment at a temperature of 15 ° C, and the alkali loss-reducing characteristics of the films were evaluated. The results are shown in FIG. At this time, the alkali reduction was carried out in an aqueous solution of 98 wt% NaOH and 1.0 wt% of NaOH. The time point when the transparent solution state became visually invisible to the naked eye was regarded as 100% reduction, and the time was recorded to evaluate the weight loss characteristics .

As can be seen from Fig. 6, the film shows a very close to the reference point of 14.2%, which means that the degree of crystallinity of all the films is maintained at a similar level. Therefore, the alkali- It is possible to evaluate it.

Further, as shown in FIG. 6, it can be seen that the alkali-reducing property of the heat-treated anionic copolymer polyester is drastically improved by only a small amount (1-3 wt%) of DBS addition, and after 5 wt% .

It can also be seen that the results in FIG. 6 are significantly different from the results and trends in FIG. 7, which shows that the introduction and content of DBS have a linear effect on the alkali loss characteristics of the amorphous film. This phenomenon means that the effect of DBS on the weight loss characteristics of the copolymer, the proper concentration and the interpretation of the kinetic considerations can be completely changed depending on the state of the sample.

Thus, although not at a level close to 100% of the actual irradiated yarn state, an assessment of the alkali loss and DBS effects in the presence of appropriate crystallinity may provide more accurate information than results obtained from the amorphous film state .

Claims (9)

An anionic copolymerized polyester, and sodium dodecylbenzene sulfonate. The method according to claim 1,
Wherein the content of sodium dodecylbenzenesulfonate is 1 to 10% by weight based on the total 100% by weight of the blend film. The method according to claim 1,
Wherein the thickness of the blend film is 10 占 퐉 to 100 占 퐉. The method according to claim 1,
Wherein the blend film has a time of less than 20 minutes for a 100% reduction in alkali in an aqueous solution of 1.0 wt% NaOH at 98 占 폚. Anionic copolymerized polyester, and sodium dodecylbenzene sulfonate. 6. The method of claim 5,
Wherein the nano filament is a sea-island type. Mixing an anionic copolymerized polyester and sodium dodecylbenzenesulfonate and melt-extruding the mixture;
Quenching the extruded mixture, cutting into chips and vacuum drying; And
And pressing the dried chip with a hot press. 8. The method of claim 7,
Wherein the content of sodium dodecylbenzenesulfonate is 1 to 10 wt% based on the total 100 wt% of the blend film. 8. The method of claim 7,
Wherein the blend film has a time required for 100% reduction in alkali in an aqueous solution of 98% C, 1.0% by weight NaOH of 20 minutes or less.

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