KR102545786B1 - Interior fiber, manufacturing method thereof, and blind including thereof - Google Patents

Abstract

The present invention provides textiles for interior use, methods for manufacturing the same, and blinds including the same. In the interior fiber containing the polyester resin of the present invention, the polyester resin includes an acid component including 70 to 80 mol% of terephthalic acid and 20 to 30 mol% of isophthalic acid; diol component; is a P-based compound; And metal sulfonate; including, but, the metal sulfonate and the P-based compound 1: 2 ~ 6 molar ratio as included in flame retardancy, low melting point characteristics, and excellent dyeability effect.

Description

Interior fiber, manufacturing method thereof, and blind including the same {Interior fiber, manufacturing method thereof, and blind including thereof}

The present invention relates to textiles, and more particularly, to interior textiles, manufacturing methods thereof, and blinds including the same.

In general, curtains, wallpaper, carpets, flame retardant non-woven fabrics, and other ornaments are made of flame retardant treated fabrics and non-woven fabrics for safety in places where people are densely populated, places with many electrical facilities, and places with many enclosed spaces. Therefore, conventional flame retardant yarns are prepared by melt-stretching chemical fiber yarn materials, and then the surface of each chemical fiber yarn is treated with a flame retardant to prevent burning due to a flame or the like. In addition, in the conventional flame retardant treatment method, the synthetic fiber yarn is woven or knitted using a loom or knitting machine to make a fabric, and then the surface of the fabric is treated with a flame retardant to prevent ignition by fire. However, conventionally, since flame retardant treatment is performed after manufacturing synthetic fiber yarns or fabrics, flame retardants are attached to the surface of synthetic fiber yarns or fabrics, so the flame retardant is likely to fall off depending on the time of use, and the flame retardant ability is improved by dropping the flame retardant. It had a downside.

Accordingly, a technology for preparing a flame retardant yarn by mixing a flame retardant component during manufacture of the flame retardant yarn has been researched and developed. However, in the polyester polymer composition having flame retardancy, the flame retardant must be evenly dispersed and distributed in the polyester resin, but the flame retardant having limited fluidity is not easily dispersed evenly inside the polyester resin, so that the desired flame retardant function cannot be obtained.

In addition, in the case of flame retardant fibers, they tend to be used for indoor interior products, and in the case of products using high-quality fabrics, high color depth is required. / or make fibers.

However, in the case of existing flame retardant fibers and/or resins for producing them, there is a problem in that physical properties of flame retardant fibers and/or fabrics prepared by additive compositions and processes for increasing color clarity are reduced. For example, Korean Patent Publication No. 2005-0103617 mentions a flame retardant polyester having excellent color development during dyeing by adding a complementary agent, but hydrolysis of the flame retardant by high-temperature hot water occurs during dyeing. There is Korean Patent Publication No. 2003-0028022 describes a method for producing polyester using cationic dyes, which requires pretreatment of metal sulfonate salts to maintain spinning processability when preparing a polyester polymer composition dyeable with cationic dyes. As a result, the process cost increases, and when the content of the modifier is increased to improve color clarity, there is a problem that causes yarn properties to deteriorate and pack pressure to increase during the process.

On the other hand, in general, synthetic fibers have a high melting point and are often limited in their use. In particular, when used as an adhesive for adhesives such as interlining or inserting between tape-shaped fabrics for bonding applications such as fibers, the textile fabric itself may be thermally deteriorated by heating, and special equipment such as a high-frequency sewing machine may be used. Because of the inconvenience of having to use it, it is desired to easily bond by a simple ordinary heat press without using such special equipment.

Conventional low-melting polyester short fibers have been widely used as hot-melt binder fibers for the purpose of bonding heterogeneous fibers in mutual fiber structures used in the manufacture of mattresses, interior materials for automobiles, or various nonwoven fabric patting applications. .

Therefore, in polyester-based resins, there is a high demand for low-melting resins, and they are used in binder fibers, adhesives, and the like. For such applications, copolymerized polyester is generally used.

For example, US Patent No. 4,129,675 introduces a low-melting polyester copolymerized using terephthalic acid (TPA) and isophthalic acid (IPA), but isophthalic acid (IPA) is expensive. Low melting point polyester using a large amount of isophthalic acid as a material has a problem of low competitiveness due to high production cost.

In addition, Japanese Patent Laid-Open Publication No. 10-298271 uses adipic acid instead of terephthalic acid in the polymerization process to increase crystallinity and heat resistance, and uses 1,4-butanediol as a diol component instead of ethylene glycol ( BD) is used to provide a fiber that increases adhesiveness and reduces the strength of the fiber even at high temperatures, but low melting point polyester manufactured using adipic acid has a melting point of 150 or less. There was a problem that it was difficult to manufacture and could not produce a lower melting point polyester.

Japanese Unexamined Patent Publication No. 10-298271

The present invention has been made to solve the above problems, it is possible to prevent the deterioration of physical properties of polyester flame retardant fibers by improving the dyeing ability of polyester resin and alleviating processing conditions such as processing temperature, excellent flame retardancy, and low An object of the present invention is to provide interior textiles that are melted at a temperature and have excellent thermal bonding strength, a method for manufacturing the same, and a blind including the same.

In the interior fiber containing a polyester resin provided in one aspect of the present invention, the polyester resin contains 70 to 80 mol% of terephthalic acid and 20 to 30 mol % of isophthalic acid an acidic component; diol component; A P-based compound represented by Formula 1 below; and a metal sulfonate; but, the metal sulfonate and the P-based compound are included in a molar ratio of 1: 2 to 6.

[Formula 1]

In Formula 1, R ¹ is -OH, -COOH, -CH ₂ COOH, -CH ₂ CH ₂ COOH, -CH ₂ CH ₂ CH ₂ COOH, or -CH ₂ CH 2 CH _{2 CH 2 COOH} .

As a preferred embodiment of the present invention, the diol component may include an aliphatic diol having 2 to 20 carbon atoms.

As a preferred embodiment of the present invention, the aliphatic diol is ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, trimethyl glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, heptamethylene glycol, octamethylene glycol , nonamethylene glycol, decamethylene glycol, undecamethylene glycol, dodecamethylene glycol and tridecamethylene glycol may include one or more selected from the group consisting of.

As a preferred embodiment of the present invention, one or more additives selected from a metal catalyst, a heat stabilizer, a chain extender, a light stabilizer, and potassium hydroxide represented by Formula 2 may be further included.

[Formula 2]

In Formula 2, R ² is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a cycloalkyl group having 5 to 6 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, or a phenyl group.

As a preferred embodiment of the present invention, the additive may include 100 to 500 ppm of the polyester resin.

As a preferred embodiment of the present invention, the acid component and the diol component may be polymerized at a molar ratio of 1:1.2 to 1.5.

As a preferred embodiment of the present invention, the compound represented by Formula 1 may be included in the polyester resin in an amount of 5,000 to 7,000 ppm (based on the P content of the compound).

As a preferred embodiment of the present invention, the melting temperature of the polyester resin is 110 to 130 ° C, and the limiting oxygen index (LOI) is 27% to 37% according to KSM ISO 4589-2. .

Another aspect of the present invention provides a method for manufacturing interior textiles. The manufacturing method includes a first step of pre-crystallizing a polyester resin at a temperature of 40 to 80 ° C. for 2 to 8 hours; a second step of removing moisture and crystallizing the pre-crystallized polyester resin at a temperature of 60 to 100 °C; and a third step of spinning the crystallized polyester resin at a temperature of 260 to 290° C. at a speed of 4,000 to 5,000 mpm, wherein the polyester resin contains 70 to 80 mol% of terephthalic acid and isophthalic acid. (isophthalic acid) acid component containing 20 to 30 mol%; diol component; A P-based compound represented by Formula 1 below; and a metal sulfonate; but, the metal sulfonate and the P-based compound are included in a molar ratio of 1:2 to 6.

[Formula 1]

In Formula 1, R ¹ is -OH, -COOH, -CH ₂ COOH, -CH ₂ CH ₂ COOH, -CH ₂ CH ₂ CH ₂ COOH, or -CH ₂ CH 2 CH _{2 CH 2 COOH} .

Another aspect of the invention provides blinds. The blind includes the interior textile according to the present invention.

The textile for interior use according to the present invention, the manufacturing method thereof, and the blind including the same are melted at a low temperature and have excellent thermal bonding strength, excellent flame retardancy, and excellent dyeability.

1 is a cross-sectional view of a blind according to an embodiment of the present invention.

Hereinafter, in order to explain the present invention in more detail, preferred embodiments according to the present invention will be described in more detail with reference to the accompanying drawings. However, the present invention is not limited to the embodiments described herein and may be embodied in other forms. Like reference numbers indicate like elements throughout the specification.

로 표현된 화학식에서, R₁은 독립적으로 수소원자, 메틸기 또는 에틸기이며, a는 1 ~ 3이다"라고 치환기에 대해 표현되어 있을 때, a가 3인 경우, 복수의 R¹, 즉 R¹ 치환기가 3개가 있고, 이들 복수 개의 R¹들 각각은 서로 같거나 다른 것으로서, R¹들 각각은 모두 수소원자, 메틸기 또는 에틸기일 수 있으며, 또는 R¹들 각각은 다른 것으로서, R¹ 중 하나는 수소원자, 다른 하나는 메틸기 및 또 다른 하나는 에틸기일 수 있음을 의미하는 것이다. 그리고, 상기 내용은 본 발명에서 표현된 치환기를 해석하는 일례로서, 다른 형태의 유사 치환기도 동일한 방법으로 해석되어야 할 것이다.In the present invention "

In the formula represented by R ₁ is independently a hydrogen atom, a methyl group or an ethyl group, and a is 1 to 3” when expressed for substituents, when a is 3, a plurality of R ¹ , that is, three R ¹ substituents, these Each of a plurality of R ¹ is the same as or different from each other, each of R ¹ may be a hydrogen atom, a methyl group or an ethyl group, or each of R ¹ is different, and one of R ¹ is It means that a hydrogen atom, the other may be a methyl group, and the other may be an ethyl group. In addition, the above information is an example of interpreting the substituents expressed in the present invention, and similar substituents of other types should be interpreted in the same way.

An interior fiber according to an embodiment of the present invention contains an acid component containing 70 to 80 mol% of terephthalic acid and 20 to 30 mol% of isophthalic acid, a diol component, and P represented by Formula 1 below. -based compound, and a metal sulfonate; but, the P-based compound and the metal sulfonate salt in a molar ratio of 1: 2 to 6.

[Formula 1]

In Formula 1, R ¹ is -OH, -COOH, -CH ₂ COOH, -CH ₂ CH ₂ COOH, -CH ₂ CH ₂ CH ₂ COOH, or -CH ₂ CH 2 CH _{2 CH 2 COOH} .

The acid component includes 70 to 80 mol% of terephthalic acid and 20 to 30 mol% of isophthalic acid. At this time, the low melting point flame retardant polyester polymer composition having excellent dyeability according to an embodiment of the present invention exhibits low melting point characteristics as it includes an acid component including the terephthalic acid and isophthalic acid. At this time, despite having a lower isophthalic acid content than the prior art according to the inclusion of the P-based compound to be described later, it can exhibit excellent low melting point characteristics.

When the content of the terephthalic acid in the acid component is less than 70 mol%, the content of isophthalic acid increases accordingly, which is uneconomical in terms of cost, and when it exceeds 80 mol%, the melting point lowering effect may be limited, resulting in adhesive properties This may be reduced, and radiation characteristics may be deteriorated during spinning.

In addition, when the content of the isophthalic acid in the acid component is less than 20 mol%, the effect of lowering the melting point may be limited, and thus adhesive properties may be deteriorated, and spinning properties may be deteriorated during spinning. When it exceeds 30 mol%, the expensive isophthalic acid content increases, so there is a disadvantage in that it is not economical in terms of cost.

The aliphatic diol may include an aliphatic diol having 2 to 20 carbon atoms. The aliphatic diol is ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, trimethyl glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, heptamethylene glycol, octamethylene glycol, nonamethylene glycol, decamethylene glycol, At least one selected from undecamethylene glycol, dodecamethylene glycol and tridecamethylene glycol may be mixed and used, more preferably at least one selected from ethylene glycol, diethylene glycol, propylene glycol and butylene glycol.

The acid component and the diol component may be reacted at a molar ratio of 1:1.2 to 1.5, more preferably at a molar ratio of 1:1.25 to 1.35. At this time, if the molar ratio of the aliphatic diol is less than 1.2, the yield of the polyester resin may be low, and if the aliphatic diol is used in a molar ratio exceeding 1.5, there is a problem in that the cost of treating the aliphatic diol increases due to unreacted aliphatic diol, which is uneconomical.

In the present invention, the compound represented by Formula 1 serves to increase the flame retardancy of the polyester resin. At the same time, as the compound represented by Formula 1 is included, the melting point lowering effect by isophthalic acid in the acid component is improved. That is, as the compound represented by Formula 1 is included in the polyester polymer composition according to an embodiment of the present invention, even if the content of isophthalic acid is low in the acid component, it can exhibit low melting point characteristics and at the same time increase flame retardancy. There is an effect that can be made.

At this time, the amount of the compound represented by Formula 1 is 5,000 to 7,000 ppm (based on the P content of the compound), preferably 5,200 to 6,500 ppm (based on the P content of the compound), based on the total weight of the mixture before polymerization. It is good to add so as to be, more preferably 5,500 ~ 6,300 ppm (based on the P content of the compound). At this time, if the input amount of the compound represented by Formula 1 is less than 5,000 ppm (based on the P content of the compound), sufficient flame retardancy may not be secured, and the melting point lowering effect may be insignificant, resulting in poor adhesion with the adherend. In addition, if it exceeds 7,000 ppm (based on the P content of the compound), poor reactivity may occur during the polymerization reaction due to the excessive P content, and problems such as decrease in heat resistance and decrease in viscosity due to weakened reactivity of the polymerization chip may occur. In the final product, deterioration of physical properties may occur, which may cause a problem of process passability due to yarn cutting during weaving and circular knitting, so it is recommended to use it within the above range.

[Formula 1]

In Formula 1, R ¹ is -OH, -COOH, -CH ₂ COOH, -CH ₂ CH ₂ COOH, -CH ₂ CH ₂ CH ₂ COOH or -CH ₂ CH ₂ CH ₂ CH ₂ COOH, preferably Wherein R ¹ is -CH ₂ COOH, -CH ₂ CH ₂ COOH, or -CH ₂ CH ₂ CH ₂ COOH.

The metal sulfonate serves to improve dyeing ability so that vivid colors can be exhibited through ionic bonding with ions in dyes, particularly cations in cationic dyes, and the amount used is 3.0 to 5.0 molar ratio with respect to 1 molar ratio of the acid component. , preferably in a molar ratio of 3.225 to 4.515, more preferably in a molar ratio of 3.5 to 4.2. At this time, if the amount of the metal sulfonate is less than 3.0 molar ratio, sufficient dyeing ability improvement effect may not be seen, and if the amount exceeds 5.0 molar ratio, the amount of the metal sulfonate is too large, so the limiting oxygen index of the polyester resin is lowered, and the flame retardant fiber There may be a problem that the mechanical properties of the lowered. In addition, the metal sulfonate may include at least one selected from the group consisting of dimethyl 5-sodiosulfo isophthalate, sodium 3,5-dicarbomethoxybenzenesulfonate and dicarbomethoxybenzenesulfonate.

In addition, the polyester polymer composition according to an embodiment of the present invention contains at least one selected from a metal catalyst represented by Formula 3, magnesium acetate, germanium acetate, and zinc acetate. A catalyst including, preferably, a metal catalyst represented by Chemical Formula 2 may be further included. In addition, when using the metal catalyst, the amount of the metal catalyst is preferably 100 to 500 ppm, preferably 150 to 400 ppm, based on the total weight of the mixture.

[Formula 2]

In Formula 3, R ² is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a cycloalkyl group having 5 to 6 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, or a phenyl group, preferably a hydrogen atom or an alkyl group having 1 to 5 carbon atoms or a cycloalkyl group of 5 to 6 carbon atoms, more preferably an alkyl group of 1 to 2 carbon atoms.

In addition, the flame retardant polyester polymer composition is a heat stabilizer, an antifoaming agent, an antioxidant, a lubricant, a light stabilizer, a hydrolysis stabilizer, a release agent, a pigment, an antistatic agent, a conductivity imparting agent, an EMI shielding agent, a magnetic imparting agent, a mineral filler, a crosslinking agent, and an antibacterial agent. , It can be prepared by further adding one or two or more additives selected from processing aids, metal deactivators, retardants, fluorine-based anti-drip agents, anti-friction agents, anti-wear agents, and coupling agents.

In the present invention, the heat stabilizer may use a general heat stabilizer used in the art, preferably trimethylphosphate, triethyl phosphate, tributyl phosphate, tributoxy 1 selected from ethyl phosphate, tricresyl phosphate, triaryl phosphate isopropylated, and hydroquinone bis-(diphenyl phosphate) A species or a mixture of two or more species may be used.

On the other hand, the method for manufacturing interior textiles according to an embodiment of the present invention includes a first step of pre-crystallizing the above-described polyester resin at a temperature of 40 to 80 ° C. for 4 to 8 hours; a second step of removing moisture and crystallizing the pre-crystallized polyester resin at a temperature of 60 to 100 °C; and a third step of spinning the crystallized polyester resin at a spinning speed of 4,000 to 5,000 mpm at a temperature of 260 to 280 °C.

In the first step, the above-mentioned polyester resin is pre-crystallized at a temperature of 40 to 80 ° C. for 4 to 8 hours. When the primary drying temperature is less than 40 ° C, pre-crystallization of the polyester resin is insignificant, and fusion may occur between the polyester resins during the second-stage drying process, and side reactions may occur when the temperature exceeds 80 ° C.

In the second step, a water removal and crystallization process is performed at a temperature of 60 to 100 ° C. At this time, when the temperature of the water removal and crystallization process is less than 60 ° C., water removal is insignificant, and fiber formation may be difficult due to hydrolysis during spinning process. can

In the third step, the water removal and crystallized polyester resin is spun at a temperature of 260 to 290 at a spinning speed of 4,000 to 5,000 mpm. At this time, when the spinning temperature condition is less than 250 ° C., fiber formation may be difficult, and when the spinning temperature condition exceeds 300 ° C., the strength characteristics of the fiber may be deteriorated.

1 is a cross-sectional view of a blind according to an embodiment of the present invention.

Referring to FIG. 1 , the blind of the present invention can be manufactured by bonding a first fabric 100 woven using interior fibers according to the present invention and a second fabric 200 that can be used for conventional blinds. At this time, the first fabric 100 and the second fabric 200 may be bonded by heat-sealing a portion of the first fabric 100 to the second fabric 200.

Hereinafter, a preferred embodiment (example) is presented to help the understanding of the present invention. However, the following examples are only for helping understanding of the present invention, and the present invention is not limited by the following experimental examples.

[ Example ]

Example 1: flame retardant polyester polymer preparation of the composition

An acid component containing 75 mol% of terephthalic acid (TPA) and 25 mol% of isophthalic acid (IPA) and ethylene glycol, which is a diol component, were added at a molar ratio of 1: 1.4, and a P system represented by the following formula (1) compound (4 mol% based on P content); and dimethyl 5-sodio sulfoisophthalate, which is a metal sulfonate, wherein the metal sulfonate and the P-based compound were mixed in a molar ratio of 1:4 to prepare a copolymerized flame retardant polyester resin.

Thereafter, after drying the polyester resin at a pre-drying temperature of 60° C. for 6 hr and a main drying temperature of 80° C., LM CD FRS-DSD 140/48 fibers were prepared at a spinning temperature of 260° C. and a spinning speed of 4,500 mpm. At this time, in order to improve the color depth, spinning is performed using a Y-type nozzle. Thereafter, weaving was performed with weft yarns (140/48) and warp yarns (280/96) using the finished interior fibers to manufacture interior fabrics.

[Formula 1]

In Formula 1, R ¹ is -CH ₂ CH ₂ COOH.

Example 2

It was prepared in the same manner as in Example 1, but lithium acetate was further added at a concentration of 300 ppm as a metal catalyst during copolymerization to prepare a polyester resin.

Example 3 to 5

It was prepared in the same manner as in Example 1, but as shown in Table 1 below, a polyester resin was prepared by changing the conditions of the terephthalate, isophthalate, diol component, P-based compound, and metal sulfonate.

comparative example 1 to 2

It was prepared in the same manner as in Example 1, but as shown in Table 1 below, a polyester resin was prepared by changing the conditions of the terephthalate, isophthalate, diol component, P-based compound, and metal sulfonate.

< Experimental example 1- Determination of melting point>

The melting point of the flame-retardant polyester compositions prepared in Examples 1 to 5 and Comparative Examples 1 to 2 was measured at room temperature through a temperature raising process.

< Experimental example 2 - Radiation Characteristics Evaluation>

The flame retardant polyester compositions prepared in Examples 1 to 5 and Comparative Examples 1 to 2 were evaluated for spinning characteristics when spinning at a spinning speed of 1350 mpm at a temperature of 280 ° C.

< Experimental example 3 - Measurement of flame retardancy>

Flame retardancy of polyester fibers was measured using a UL 94-AVH chamber according to the KS M 3305 method.

Example 1 Example 2 Example 3 Example 4 Example 5 Comparative Example 1 Comparative Example 2 acid component TPA content (mol %) 75 75 71 78 75 75 90 IPA content (mol%) 25 25 29 22 25 25 10 Acid component: diol component molar ratio 1:1.4 1:1.4 1:1.4 1:1.4 1:1.4 1:1.4 1:1.4 Inclusion of metal catalyst × ○ × × × × × P-based compound content (mol% based on P content) 4 4 4 4 6 × 4
Metal sulfonate: P-based compound molar ratio 1:4 1:4 1:4 1:4 1:4 - 1:4 melting point (℃) 112 110 114 116 110 158 150 Limiting Oxygen Index (%) 33 35 32 33 36 25.6 24 Flame retardant ¹⁾ V1 V1 V1 V1 V1 V2 V2 Radiation characteristics ²⁾ ◎ ○ ○ ◎ ◎ × △ 1) V1: Excellent V2: Fair
2) ◎: Excellent, ○: Excellent, △: Normal, ×: Poor

In the above, the present invention has been described in detail with preferred embodiments and experimental examples, but the present invention is not limited by the above embodiments and experimental examples, and those skilled in the art within the technical spirit and scope of the present invention Various modifications and changes are possible by the person.

Claims (10)

In the interior fiber containing a polyester resin having a melting temperature of 110 ~ 130 ℃,
The polyester resin,
An acid component containing 70 to 80 mol% of terephthalic acid and 20 to 30 mol% of isophthalic acid;
diol component;
A P-based compound represented by Formula 1 below; and
A metal sulfonate salt containing at least one selected from the group consisting of dimethyl 5-sodiosulfoisophthalate and sodium 3,5-dicarbomethoxybenzenesulfonate;
A polyester resin copolymerized with the metal sulfonate and the P-based compound in a molar ratio of 1: 2 to 6,
The acid component and the diol component are included in a molar ratio of 1:1.2 to 1.4,
The diol is a non-polyol diol, ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, trimethyl glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, heptamethylene glycol, octamethylene glycol, nonamethylene An interior textile characterized by comprising an aliphatic diol containing at least one selected from the group consisting of glycol, decamethylene glycol, undecamethylene glycol, dodecamethylene glycol and tridecamethylene glycol.
[Formula 1]

In Formula 1, R ¹ is -OH, -COOH, -CH ₂ COOH, -CH ₂ CH ₂ COOH, -CH ₂ CH ₂ CH ₂ COOH, or -CH ₂ CH 2 CH _{2 CH 2 COOH} . delete delete The interior textile according to claim 1, further comprising at least one additive selected from a metal catalyst, a heat stabilizer, a chain extender, a light stabilizer, and potassium hydroxide represented by Formula 2 below.
[Formula 2]

In Formula 2, R ² is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a cycloalkyl group having 5 to 6 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, or a phenyl group. According to claim 4,
The additive is an interior fiber comprising 100 to 500 ppm of the polyester resin. delete According to claim 1,
Interior textiles containing the compound represented by Formula 1 in an amount of 5,000 to 7,000 ppm (based on the P content of the compound) in the polyester resin. According to claim 1,
An interior textile with a limiting oxygen index (LOI) of 27% to 37% in accordance with KSM ISO 4589-2. Step 1 of pre-crystallizing the polyester resin composition at a temperature of 40 to 80 ° C. for 2 to 8 hours;
Step 2 of preparing a crystallized polyester resin by removing moisture and crystallizing the pre-crystallized polyester resin composition at a temperature of 60 to 100 ° C; and
A third step of spinning the crystallized polyester resin at a spinning speed of 4,000 to 5,000 mpm at a temperature of 260 to 290 ° C; including,
The polyester resin composition of step 1,
An acid component containing 70 to 80 mol% of terephthalic acid and 20 to 30 mol% of isophthalic acid;
diol component;
A P-based compound represented by Formula 1 below; and
A metal sulfonate salt containing at least one selected from the group consisting of dimethyl 5-sodiosulfoisophthalate and sodium 3,5-dicarbomethoxybenzenesulfonate; metal sulfonate; including,
The metal sulfonate and the P-based compound are included in a molar ratio of 1: 2 to 6,
The crystallized polyester resin in step 3 has a melting temperature of 110 to 130 ° C,
The acid component and the diol component are included in a molar ratio of 1:1.2 to 1.4,
The diol is a non-polyol diol, ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, trimethyl glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, heptamethylene glycol, octamethylene glycol, nonamethylene A method for producing an interior textile, characterized in that it comprises an aliphatic diol containing at least one selected from the group consisting of glycol, decamethylene glycol, undecamethylene glycol, dodecamethylene glycol and tridecamethylene glycol.
[Formula 1]

In Formula 1, R ¹ is -OH, -COOH, -CH ₂ COOH, -CH ₂ CH ₂ COOH, -CH ₂ CH ₂ CH ₂ COOH, or -CH ₂ CH 2 CH _{2 CH 2 COOH} . Claims 1, 4, 5, 7 and 8 selected from any one of the interior textiles for blinds comprising a textile.

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