KR930003368B1 - Polyphenylene sulfide conjugated fiber - Google Patents
Polyphenylene sulfide conjugated fiber Download PDFInfo
- Publication number
- KR930003368B1 KR930003368B1 KR1019900019962A KR900019962A KR930003368B1 KR 930003368 B1 KR930003368 B1 KR 930003368B1 KR 1019900019962 A KR1019900019962 A KR 1019900019962A KR 900019962 A KR900019962 A KR 900019962A KR 930003368 B1 KR930003368 B1 KR 930003368B1
- Authority
- KR
- South Korea
- Prior art keywords
- pps
- core
- component
- polyphenylene sulfide
- fiber
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/28—Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
- D01D5/30—Conjugate filaments; Spinnerette packs therefor
- D01D5/34—Core-skin structure; Spinnerette packs therefor
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
제1도는 본 발명 섬유의 횡단면 구성도.1 is a cross-sectional configuration of the present invention fiber.
* 도면의 주요부분에 대한 부호의 설명* Explanation of symbols for main parts of the drawings
C : 코아성분 S : 시스성분C: Core component S: Sheath component
J : 복합섬유J: Composite Fiber
본 발명은 내열성 및 내약품성이 우수한 폴리페닐렌 설파이드(이하 PPS라 칭함) 복합섬유에 관한 것으로, 특히, 시스-코아 복합방사법을 사용하여 PPS와 다른 중합체를 복합방사함으로써 PPS 섬유의 우수한 특성을 그대로 유지토록 하려는 것이다. 일반적으로 PPS 섬유는 내열성, 내약품성 등 우수한 특성으로 인하여 산업용 섬유로서 사용이 급속히 신장되고 있으나, 중합체의 가격이 비싸 이로인한 제조경비가 높아 사용상 많은 제약이 따르게 되었다.The present invention relates to a polyphenylene sulfide (hereinafter referred to as PPS) composite fiber having excellent heat resistance and chemical resistance, and in particular, the excellent properties of PPS fibers are maintained as they are by splicing PPS and other polymers by using a cis-core composite spinning method. It is to be maintained. In general, PPS fiber is rapidly being used as an industrial fiber due to its excellent properties such as heat resistance and chemical resistance, but due to the high production cost due to the high cost of the polymer, many constraints have been placed on use.
이러한 단점을 해결하기 위해 종래에는 다른 고분자와 블렌딩하여 혼합방사하거나 또는 PPS를 커버링사(絲)로서 사용하였으나 이는 모두 PPS 섬유의 특성인 내열성 또는 내약품성을 유지하는데 한계가 따르거나 상기의 제조경비를 크게 절감시키지 못하는 문제점이 있었다.In order to solve this disadvantage, conventionally, blended spinning with other polymers or mixed spinning or PPS was used as a covering yarn, but all of them have limitations in maintaining heat resistance or chemical resistance, which are characteristics of PPS fibers, There was a problem that can not greatly reduce.
따라서 본 발명에서는 PPS 중합체와 다른 중합체를 시스-코아 복합방사법에 의해 복합섬유로 제조함으로써, PPS 섬유의 우수한 특성은 그대로 유지함과 아울러 제조경비 또한 절감시키려 함에 그 목적이 있는 것이다.Therefore, in the present invention, the PPS polymer and other polymers are prepared by the composite fiber by the cis-core composite spinning method, to maintain the excellent properties of the PPS fibers as well as to reduce the manufacturing cost.
이하 첨부된 도면과 관련하여 상세히 설명하면 다음과 같다.Hereinafter will be described in detail with reference to the accompanying drawings.
제1도는 본 발명에 의해 제조된 복함섬유의 횡단면 구성도로서, 본 발명에서 언급하고 있는 시스성분과 코아성분은 제1도에서와 같이 복합섬유(J) 횡단면도의 중심부를 코아성분(C)이라 하고, 외곽부는 시스성분(S)이라 한다.1 is a cross-sectional configuration of the composite fiber produced by the present invention, the cis component and the core component referred to in the present invention is the core of the cross-sectional view of the composite fiber (J) as in FIG. The outer portion is referred to as the sheath component (S).
상기 코아성분(C)에는 플레에스터, 폴리아마이드, 폴리올레핀 등 용융방사 가능한 중합체를 사용하고 시스성분(S)에는 멜트플로인댁스(Melt Flow Index : 이하 MI라 칭함)가 5∼300g/10min(ASTM-D-1238-70)인 PPS 중합체를 사용하되, 시스성분인 PPS는 하기의 일반식과 같은 구조를 가지며,The core component (C) is a melt-spun polymer such as polyester, polyamide, polyolefin, etc., and the sheath component (S) has a melt flow index (hereinafter referred to as MI) of 5 to 300 g / 10 min ( PPS polymer of ASTM-D-1238-70) is used, but the cis component PPS has a structure as shown in the following general formula,
단, m : n=100 : 0-50 : 50(몰비)However, m: n = 100: 0-50: 50 (molar ratio)
상기한 바에서 MI가 5이하 또는 300을 초과시에는 제사가 곤란하며, 바람직하게는 MI 50∼200인 중합체를 사용하여 통상의 시스-코아 복합방사법으로 섬유를 제조한다. 이때 시스성분은 전체 면적비율로 30∼70%이고, 나머지는 면적비율은 코아성분일때 공정성은 양호하면서 PPS의 특성인 내약품성을 그대로 유지하는 섬유를 제조할수 있다.As described above, when the MI is less than 5 or more than 300, it is difficult to make a yarn, and fibers are prepared by conventional cis-core composite spinning using a polymer having a MI of 50 to 200. At this time, the sheath component is 30 to 70% in the total area ratio, and the remainder in the core ratio is the core component can be produced a fiber that has good processability while maintaining the chemical resistance characteristics of the PPS.
그러나 시스성분이 전체 면적비율의 30% 이하일 경우 즉, 코아성분이 70% 이상이 되면 코아성분이 섬유상에서 한쪽으로 치우치거나 섬유표면으로 돌출되는 현상이 발생하여 결과적으로 전체 섬유의 내약품성이 저하된다.However, if the sheath component is 30% or less of the total area ratio, that is, the core component is 70% or more, the core component may be biased to one side or protrude to the fiber surface, resulting in a decrease in chemical resistance of the entire fiber. do.
또 시스성분이 전체 면적비율의 70% 이상일 경우 즉, 코아성분이 30% 이하로 되면 방사시 코아성분이 섬유 중심축에 자리잡기가 어려우며 제조경비의 절감효과도 크지 못하게 된다.In addition, when the sheath component is 70% or more of the total area ratio, that is, the core component is less than 30%, the core component is difficult to settle on the fiber central axis during spinning, and the effect of reducing the manufacturing cost is not great.
따라서 상기와 같은 본 발명의 적용조건으로 복합방사에 의해 PPS 섬유를 제조할 경우 단독방사로 제조한 PPS 섬유에 비해 제조경비가 크게 절감되면서 PPS의 특성인 우수한 내열성, 내약품성 등을 그대로 유지할 수 있으므로 요구되는 산업용 섬유분야에서 경제적으로 사용할 수 있는 효과를 갖게 되는 것이다.Therefore, when manufacturing PPS fiber by the composite spinning according to the application conditions of the present invention as described above, it is possible to maintain the excellent heat resistance, chemical resistance, etc. of the characteristics of the PPS while significantly reducing the manufacturing cost compared to the PPS fiber produced by single spinning It will have an effect that can be used economically in the field of industrial textiles required.
이하 본 발명을 실시예 및 비교예를 통하여 보다 구체적으로 설명하면 다음과 같다.Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples.
[실시예 1∼2 비교예 1∼4]EXAMPLES 1-2 Comparative Examples 1-4
[방사 및 연신][Spinning and Drawing]
본 실시예에서 사용한 방사기는 통상의 시스-코아 복합방사기를 사용하고, 헤드의 온도 300℃에서 통상의 시스-코아 복합 방사구금으로 방사하여 800m/min의 속도로 권취하였다.The spinning machine used in this example was wound at a speed of 800 m / min using a conventional cis-core composite spinning machine and spinning with a typical cis-core composite spinneret at a head temperature of 300 ° C.
이렇게 얻은 미연신사를 역시 통상의 연신기를 사용하여 히트롤러(Heat Roller) 90℃, 히트프레이트(Heat Plate) 190℃, 400m/min의 속도로 2.5배 연신하였다.The undrawn yarn thus obtained was stretched 2.5 times at a speed of Heat Roller 90 ° C., Heat Plate 190 ° C. and 400 m / min using a conventional drawing machine.
내열성 테스트 :Heat resistance test:
230℃ 오븐에 시료를 24시간 방치한 후 강도 유지율을 측정하였다.After leaving the sample in the oven at 230 ° C. for 24 hours, the strength retention was measured.
내약품성 테스트 :Chemical resistance test:
50% 황산 및 10% 수산화나트륨에 93℃에서 24시간 방치한 후 강도 유지율을 측정하였다.The strength retention was measured after standing in 50% sulfuric acid and 10% sodium hydroxide for 24 hours at 93 ° C.
[실시예 1]Example 1
시스성분에는 MI 100(315℃, 하중 5,000g, ASTM-D-1238-70)인 PPS를, 코아성분에는 고유점도 0.64인 PET를 사용하여 시스성분과 코아성분의 면적비가 50 : 50이고 75D/24F인 복합섬유를 제조한 후 이 복합섬유를 내열성 및 내약품성 테스트를 실시하여 그 결과를 표 1,2에 나타내었다.The sheath component is MI 100 (315 ℃, 5,000g load, ASTM-D-1238-70) PPS, and the core component is PET with intrinsic viscosity 0.64, and the area ratio of the sheath component and the core component is 50:50 and 75D / After manufacturing the composite fiber of 24F, the composite fiber was subjected to heat resistance and chemical resistance test, and the results are shown in Table 1,2.
[실시예 2]Example 2
시스성분에는 MI 100인 PPS를, 코아성분에는 개미산중 상대점도 45인 나일론 66을 사용하여 시스성분과 코아성분의 면적비가 50 : 50이고 75D/24F인 복합섬유를 제조한 후, 내열성 및 내약품성 테스트를 실시하여 그 결과를 표 1,2에 나타내었다.PPS of MI 100 for the sheath component and nylon 66 having a relative viscosity of 45 formic acid were used for the core component to produce a composite fiber having an area ratio of 50:50 and 75D / 24F, and then heat and chemical resistance. The test was carried out and the results are shown in Table 1,2.
[비교예 1]Comparative Example 1
고유점도 0.64인 폴리에스터를 통상의 방사구금을 사용하여 75D/24F인 섬유를 제조한 후 내열성 및 내약품성 테스트를 실시하여 그 결과를 표 1,2에 나타내었다.A polyester having an intrinsic viscosity of 0.64 was used to prepare a fiber having 75D / 24F using a conventional spinneret, and then subjected to a heat resistance and chemical resistance test. The results are shown in Tables 1 and 2 below.
[비교예 2]Comparative Example 2
개미산중 상대점도 45인 나일론 66을 통상의 단독 방사구금을 사용하여 75D/24F인 섬유를 제조한 후 내열성 및 내약품성 테스트를 실시하여 그 결과를 표 1,2에 나타내었다.Nylon 66 having a relative viscosity of 45 in formic acid was prepared using 75 D / 24F fiber using a conventional single spinneret, and then subjected to heat and chemical resistance tests. The results are shown in Tables 1 and 2 below.
[비교예 3]Comparative Example 3
실시예 1과 같은 시스-코아 방사구금을 사용하고 시스성분에는 MI 100인 PPS를, 코아성분에는 고유점도 0.64인 PET를 사용하여 시스성분과 코아성분의 면적비가 20 : 80이고 75D/24F인 복합섬유를 제조하되, 내열성 및 내약품성 테스트를 실시한 후 강도 유지율을 측정하여 표 1,2에 나타내었다.Using the same cis-core spinneret as in Example 1 and PPS with MI 100 for the sheath component and PET with an intrinsic viscosity of 0.64 for the core component, the area ratio of the cis component to the core component is 20:80 and 75D / 24F. Fibers were prepared, but the strength retention was measured after heat resistance and chemical resistance tests.
[비교예 4][Comparative Example 4]
실시예 1과 같은 시스-코아 방사구금을 사용하여 시스성분에는 MI 100인 PPS를, 코아성분에는 상대점도 45인 나일론 66을 사용하여 시스성분과 코아성분의 면적비가 20 : 80이고 75D/24F인 복합섬유를 제조하되, 내열성 및 내약품성 테스트를 실시한 후, 그 결과를 측정하여 표 1,2에 나타내었다.Using the same cis-core spinneret as in Example 1, PPS having a MI 100 in the sheath component and nylon 66 having a relative viscosity of 45 in the core component were used, and the area ratio of the cis component to the core component was 20:80 and 75D / 24F. To prepare a composite fiber, after performing a heat resistance and chemical resistance test, the results are measured and shown in Table 1,2.
[표 1]TABLE 1
내열성 테스트Heat resistance test
[표 2]TABLE 2
내약품성 테스트Chemical resistance test
표 1,2의 강도 유지율은 내열성 및 내약품성 테스트전의 원사강도가 3∼4g/D'e, 신도가 30% 내외인 것을 사용하였을 때의 수치를 나타내며, 강도 유지율은 하기와 같은 식에 의해 구하였다.The strength retention of Table 1,2 shows the numerical value when the yarn strength of 3-4g / D'e and the elongation is about 30% before heat resistance and chemical-resistance test were used, and the strength retention is calculated by the following formula. It was.
강도 유지율(%)= Strength retention rate (%)
상기 표 1,2의 검토결과 시스성분인 PPS를 단독으로 사용하였을때의 강도 유지율을 100%로 기준하였을때 본 발명의 적용조건인 시스성분이 면적비율 30∼70%에서는 단독방사로 제조한 PPS 섬유에 비해 제조경비가 크게 절감되면서 PPS의 특성인 우수한 내열성, 내약품성을 유지할 수 있었다.As a result of the examination of Tables 1 and 2, when the strength retention rate when the PPS as the sheath component was used alone was 100%, the sheath component as the application condition of the present invention had an area ratio of 30 to 70%. The manufacturing cost was significantly reduced compared to the fiber, and the excellent heat resistance and chemical resistance of PPS were maintained.
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019900019962A KR930003368B1 (en) | 1990-12-05 | 1990-12-05 | Polyphenylene sulfide conjugated fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019900019962A KR930003368B1 (en) | 1990-12-05 | 1990-12-05 | Polyphenylene sulfide conjugated fiber |
Publications (2)
Publication Number | Publication Date |
---|---|
KR920012561A KR920012561A (en) | 1992-07-27 |
KR930003368B1 true KR930003368B1 (en) | 1993-04-26 |
Family
ID=19307086
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900019962A KR930003368B1 (en) | 1990-12-05 | 1990-12-05 | Polyphenylene sulfide conjugated fiber |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR930003368B1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011115320A1 (en) * | 2010-03-15 | 2011-09-22 | 코오롱글로텍 주식회사 | Outstandingly flame retardant and sunlight fast conjugate fibre and an interior fabric using the same |
KR101243613B1 (en) * | 2010-07-30 | 2013-03-14 | (주)우노 앤 컴퍼니 | Polyphenylene Sulfide Synthetic Hair Filament and Process for Preparing the Same |
WO2014134020A1 (en) * | 2013-02-27 | 2014-09-04 | Bha Altair, Llc | Bi-component fiber and filter media including bi-component fibers |
KR20190005021A (en) * | 2017-07-05 | 2019-01-15 | 주식회사 휴비스 | Rubber Composite Containing Polyphenylene Sulfide Conjugated Fiber |
KR20190023414A (en) * | 2017-08-29 | 2019-03-08 | 주식회사 휴비스 | Insulating Paper Containing Polyphenylene Sulfide Conjugated Fiber |
-
1990
- 1990-12-05 KR KR1019900019962A patent/KR930003368B1/en not_active IP Right Cessation
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011115320A1 (en) * | 2010-03-15 | 2011-09-22 | 코오롱글로텍 주식회사 | Outstandingly flame retardant and sunlight fast conjugate fibre and an interior fabric using the same |
KR101156193B1 (en) * | 2010-03-15 | 2012-06-18 | 코오롱글로텍주식회사 | Conjugated fiber having excellent flame resistance and light fastness and interior fabric using the same |
US9181638B2 (en) | 2010-03-15 | 2015-11-10 | Kolon Glotech, Inc. | Conjugated fiber having excellent flame retardancy and color fastness and interior fabric using the same |
KR101243613B1 (en) * | 2010-07-30 | 2013-03-14 | (주)우노 앤 컴퍼니 | Polyphenylene Sulfide Synthetic Hair Filament and Process for Preparing the Same |
WO2014134020A1 (en) * | 2013-02-27 | 2014-09-04 | Bha Altair, Llc | Bi-component fiber and filter media including bi-component fibers |
US8951325B2 (en) | 2013-02-27 | 2015-02-10 | Bha Altair, Llc | Bi-component fiber and filter media including bi-component fibers |
KR20190005021A (en) * | 2017-07-05 | 2019-01-15 | 주식회사 휴비스 | Rubber Composite Containing Polyphenylene Sulfide Conjugated Fiber |
KR20190023414A (en) * | 2017-08-29 | 2019-03-08 | 주식회사 휴비스 | Insulating Paper Containing Polyphenylene Sulfide Conjugated Fiber |
Also Published As
Publication number | Publication date |
---|---|
KR920012561A (en) | 1992-07-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0453100B1 (en) | Poly(phenylene sulfide) fibers and production process thereof | |
US5911930A (en) | Solvent spinning of fibers containing an intrinsically conductive polymer | |
US3397107A (en) | Composite polyamide filaments with improved potential crimpability and method of making the same | |
US5788897A (en) | Electrically conductive fibers | |
KR930003368B1 (en) | Polyphenylene sulfide conjugated fiber | |
JP4374409B2 (en) | Cable protection sleeve | |
US4970038A (en) | Process of preparing polyester yarn | |
US5882566A (en) | Method for preparing a high strength, high modulus electrically conductive fiber | |
JPH0299614A (en) | Heat-resistant, chemical resistant conjugated fiber of improved releasability | |
JPS62299513A (en) | Production of polyphenylene sulfide monofilament | |
JP2878470B2 (en) | Polyphenylene sulfide fiber and method for producing the same | |
KR100356674B1 (en) | Method for producing two-color polyester conjugated filament | |
US6093319A (en) | Poly (arylene sulfide) compositions and manufactures | |
EP0870080B1 (en) | Electrically conductive fibers | |
KR950001653B1 (en) | Manufacturing process for polyester composite fiber having crimp tendency | |
KR101110105B1 (en) | A technical polyester fiber with high toughness and a method for manufacturing the same | |
JP2009030205A (en) | Polyphenylene sulfide monofilament for cable-protecting sleeve and cable-protecting sleeve produced from polyphenylene sulfide | |
JPH04327214A (en) | Conjugate fiber | |
KR870000592B1 (en) | Method of making anti-static polyester fiber | |
JPH11323661A (en) | Polyester filament and its production | |
JP2023051860A (en) | Polyether sulfone fiber, fiber package, nonwoven fabric, and manufacturing method of polyether sulfone fiber | |
DE69024811T2 (en) | High strength fibers or films made from aromatic copolyamides with free carboxyl groups | |
JPH0345711A (en) | Polyphenylene sulphide-made monofilament for wire of paper-making machine | |
KR980009557A (en) | Method for producing polyester-based composite fiber | |
JPS591719A (en) | Machine sewing thread |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
G160 | Decision to publish patent application | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20040409 Year of fee payment: 12 |
|
LAPS | Lapse due to unpaid annual fee |