KR100426588B1 - A method of preparing for a sea-island typed composit fiber used in warp knitting - Google Patents
A method of preparing for a sea-island typed composit fiber used in warp knitting Download PDFInfo
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- KR100426588B1 KR100426588B1 KR10-2001-0020100A KR20010020100A KR100426588B1 KR 100426588 B1 KR100426588 B1 KR 100426588B1 KR 20010020100 A KR20010020100 A KR 20010020100A KR 100426588 B1 KR100426588 B1 KR 100426588B1
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- 239000000835 fiber Substances 0.000 title claims abstract description 39
- 238000009940 knitting Methods 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 title claims description 34
- 239000002131 composite material Substances 0.000 claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 claims abstract description 21
- 238000010828 elution Methods 0.000 claims abstract description 16
- 229920000728 polyester Polymers 0.000 claims abstract description 16
- 229920001634 Copolyester Polymers 0.000 claims abstract description 4
- 239000013078 crystal Substances 0.000 claims description 13
- 238000004090 dissolution Methods 0.000 claims description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 12
- 238000009987 spinning Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 239000012670 alkaline solution Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 229920001410 Microfiber Polymers 0.000 description 4
- 230000001680 brushing effect Effects 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- -1 dimethylisophthalate sulfonate salt Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000009966 trimming Methods 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010036 direct spinning Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229940068917 polyethylene glycols Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
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
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
-
- 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)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Multicomponent Fibers (AREA)
Abstract
본 발명은 경편용 해도형 복합섬유의 제조방법에 관한 것으로서, 알칼리 이용해성의 공중합 폴리에스테르를 해성분으로 사용하고 통상의 폴리에스테르를 도성분으로 사용하여 방사 직접 연신 방식으로 50∼90데니어의 경편용 해도형 복합섬유를 제조할때, 아래 조건을 동시에 충족시킴을 특징으로 한다.The present invention relates to a method for producing a warp island-in-the-sea composite fiber, and using 50-90 denier for warp knitting using an alkali-soluble copolyester as a sea component and a conventional polyester as a sea component. When manufacturing island-in-the-sea composite fiber, the following conditions are simultaneously satisfied.
- 아 래 --Below-
·제1고뎃로울러의 속도(V1) : 1,000m/분∼3,000m/분Speed of the first high roller (V 1 ): 1,000 m / min to 3,000 m / min
·제2고뎃로울러의 속도(V2) : 4,000m/분∼6,000m/분Speed of the second high roller (V 2 ): 4,000m / min to 6,000m / min
·제1고뎃로울러 상의 원사모듈러스 ≤ 20g/dYarn modulus on the first high roller ≤ 20 g / d
·제2고뎃로울러 상의 원사결정화도 : 25∼45%Yarn crystallinity on the second high roller: 25 to 45%
본 발명으로 제조한 해도형 복합섬유는 해성분 용출후 원사 모듈러스가 우수하여 기모시 원사 손상이 최소화되어 경편지의 촉감 및 외관을 향상 시킨다.The island-in-the-sea composite fiber prepared by the present invention has excellent yarn modulus after elution of sea component, thereby minimizing yarn damage during raising, thereby improving the feel and appearance of warp knitted paper.
Description
본 발명은 경편용 해도형 복합섬유에 관한 것이다.The present invention relates to a island-in-the-sea composite fiber for warp knitting.
해도형 복합섬유는 알칼리 이용해성(易容解性) 폴리머를 해성분으로 사용하고 섬유형성성 폴리머를 도성분으로 사용하여 이들을 해도형으로 복합 방사하여 제조되며, 주로 극세섬유를 제조하기 위한 목적으로 생산되고 있다. 다시 말해 해도형 복합섬유 제조후 이를 알칼리 용액으로 처리하여 알칼리 이용해성 폴리머인 해성분을 용출하므로서 도성분만으로 구성되는 극세섬유를 제조하게 된다.The island-in-the-sea composite fiber is manufactured by using an alkali-soluble polymer as a sea component and a fiber-forming polymer as a island component, and composite spinning them into an island-in-the-sea type, mainly for the purpose of producing ultrafine fibers. Is being produced. In other words, after preparing the island-in-the-sea composite fiber, it is treated with an alkaline solution to elute the sea component which is an alkali-soluble polymer, thereby producing an ultrafine fiber composed only of the island component.
이와 같이 해도형 복합섬유로부터 극세섬유를 제조하는 방법은 직접방사로 극세섬유를 제조하는 방법에 비해 방사 및 연신조업성이 우수하고 보다 세섬도인 극세섬유를 얻을 수 있는 장점이 있는 한편, 제직 또는 편직후 가공공정에서 해성분 폴리머를 유기용제 등으로 용출, 제거하는 공정이 필요하다. 따라서 해성분 폴리머는 유기용제 또는 용액에서 쉽게 용해되는 특성과 해성분 용출후의 원사 모듈러스가 매우 중요하다.As described above, the method of manufacturing the ultrafine fibers from the island-in-the-sea composite fiber has the advantages of superior spinning and stretching operations and more fineness of fine fibers compared to the method of manufacturing the ultrafine fibers by direct spinning. After knitting, the process of eluting and removing the sea component polymer with an organic solvent in a processing step is required. Therefore, the sea component polymer is very important to be easily dissolved in an organic solvent or a solution, and yarn modulus after sea component elution.
일반적으로 해도형 복합섬유에 사용되는 해성분 폴리머로는 알칼리 이용해성 공중합 폴리에스테르가 주로 사용된다. 그 이유는 특수 장치 및 회수 처리 비용이 많이 드는 유기용제를 사용하지 않고도 일반 폴리에스테르 직물의 감량 가공에 널리 적용되는 알칼리 용액 및 감량 설비에서 해성분의 용출이 가능하기 때문이다.In general, alkali-soluble copolyester is mainly used as the sea component polymer used in the island-in-the-sea composite fiber. The reason for this is that the dissolution of the sea component is possible in alkaline solutions and weight reduction facilities which are widely applied in weight reduction processing of general polyester fabrics without the use of special equipment and costly organic solvents.
도성분 폴리머가 나일론인 경우 해성분 용출시 나일론이 알칼리 용액에 의해 침해되는 정도가 매우 낮기 때문에 해성분의 용출 속도는 크게 중요하지 않으나, 도성분이 폴리에스테르인 경우는 알칼리에 취약하므로 해성분의 용출 속도가 낮은 경우 해성분이 완전히 용출되기 전에 도성분이 침해되어 용출후 원사강도가 급격히 저하된다. 이로 인해 기모성이 불량하게 되며 목표하는 최종 제품의 외관,촉감이 발현되기 곤란하다.When the water-based polymer is nylon, the dissolution rate of the sea component is not very important because the degree of nylon invasion by the alkaline solution is very low when the sea component is eluted. If the speed is low, the island component is violated before the sea component is completely eluted, and the yarn strength is drastically lowered after the dissolution. As a result, the raising properties are poor and it is difficult to express the appearance and feel of the target final product.
반면 해성분의 용출속도가 빠르면 상기 문제들의 발생을 억제할 수 있을 뿐만 아니라 알칼리 농도,용출온도 및 시간을 감소시킬 수 있기 때문에 용출 비용의 절감과 함께 생산성을 증대시킬 수 있는 장점도 있다. 그러나 해성분의 용출 속도를 높이기 위해서는 공중합 화합물의 함량을 증가시켜야 하나, 과다하게 공중합 화합물의 함량이 증가하면 용출성은 향상되는 반면 폴리머의 융점이 없어지고 연화점만이 존재하는 무정형 폴리머가 되어 제사하는 것이 곤란하게 된다. 또한 원사의 용출전 강도가 저하되어 기모시 기모가 서로 엉키는 불량이 발생하며 공중합 화합물의 투입 증가로 폴리머 제조원가가 상승하는 단점이 발생한다.On the other hand, if the dissolution rate of the sea component is fast, not only the occurrence of the above problems can be suppressed, but also the alkali concentration, elution temperature and time can be reduced, thereby reducing the elution cost and increasing productivity. However, in order to increase the dissolution rate of the sea component, the content of the copolymer compound should be increased. However, when the content of the copolymer compound is excessively increased, the elution property is improved, but the melting point of the polymer is eliminated and it is an amorphous polymer having only a softening point. It becomes difficult. In addition, the yarn before the eluting strength is lowered, the brushing occurs when the brush is entangled with each other, and the polymer manufacturing cost increases due to the increased input of the copolymer compound.
해도형 복합섬유 제조에 사용되는 알칼리 이용출성 폴리에스테르를 제조하는 종래 기술로서는, 첫째 폴리에스테르 중합공정 중에 디메틸이소프탈레이트 술포네이트 솔트(이하 "DMIS"라고 한다) 또는 저분자량의 폴리알킬렌글리콜(이하 "PAG"라고 한다)을 공중합 시키는 방법과, 둘째 폴리에스테르와 고분자량의 PAG를 블랜딩 하는 방법과 셋째 폴리에스테르 중합체와 고분자량의 PAG를 블랜딩 하는 방법들이 알려져 있다.Conventional techniques for producing alkali-soluble polyesters used in the preparation of island-in-the-sea composite fibers include, firstly, dimethylisophthalate sulfonate salt (hereinafter referred to as "DMIS") or low molecular weight polyalkylene glycols (hereinafter referred to as "polyester") during the polyester polymerization process. The method of copolymerizing "PAG", the method of blending the second polyester and the high molecular weight PAG, and the method of blending the third polyester polymer and the high molecular weight PAG are known.
이상에서 설명한 알칼리 이용출성 폴리에스테르를 해성분으로 사용하고 폴리에스테르를 도성분으로 사용하여 통상의 방사 직접 연신 방법으로 제조한 종래의 해도형 복합섬유들은 해성분 용출과정에서 도성분이 알칼리 용액에 의해 많이 손상되어 해성분 용출후의 원사 결정배향도가 불량한 문제가 있다. 그 결과 경편후 계속되는 기모공정에서 원사가 심하게 손상, 탈락되어 기모성이 저하되고 경편지의 외관 및 품질이 나빠지는 문제가 있었다.Conventional islands-in-the-sea composite fibers prepared by the conventional spinning direct stretching method using the alkali-soluble leaching polyester described above as the sea component and the polyester as the island component have a high degree of the island component by the alkaline solution during the sea component elution process. There is a problem in that the yarn crystal orientation after damage is eluted. As a result, in the subsequent raising process after warp knitting, the yarn was severely damaged and dropped, resulting in a deterioration in brushing and deteriorating the appearance and quality of the warp knit.
본 발명의 목적은 이와 같은 문제점을 해결하기 위하여 해성분 용출후의 원사 결정배향도가 우수하여 경편용 원사로 특히 유용한 해도형 복합섬유의 제조방법을 제공하기 위한 것이다.It is an object of the present invention to provide a method for producing island-in-the-sea composite fibers which are particularly useful as warp yarns because of excellent yarn crystal orientation after sea component elution to solve such problems.
본 발명은 해성분 용출 및 기모공정에서 원사 결정배향도의 저하를 최소화 하기 위하여 제1고뎃로울러 및 제2고뎃로울러의 속도, 제사공정중의 원사물성을 적절하게 조절하는 방법을 제공하고자 한다. 구체적으로 제사공정의 각 단계별 원사 모듈러스, 결정화도 및 복굴절률을 적정 범위로 콘드롤 하므로서, 해성분 용출 또는 기모시 원사의 물성저하를 최소화 시키는 방법을 제공하고자 한다. 또한 본 발명은 경편용 원사로 특히 적합한 해도형 복합섬유를 제조하는 방법을 제공하고자 한다.The present invention is to provide a method for appropriately controlling the speed of the first high roller and the second high roller, the yarn physical properties during the weaving process in order to minimize the degradation of the yarn crystal orientation in the sea component dissolution and raising process. Specifically, by controlling the yarn modulus, crystallinity, and birefringence of each step of the weaving process to an appropriate range, it is intended to provide a method of minimizing the physical property degradation of the yarn during dissolution or raising the sea component. In another aspect, the present invention is to provide a method for producing an island-in-the-sea composite fiber particularly suitable as warp yarn.
도 1은 본 발명의 공정 개략도1 is a process schematic diagram of the present invention
※도면중 주요부분에 대한 부호 설명※ Explanation of main parts in drawings
1 : 방사구금 2 : 제1고뎃로울러 3 : 제2고뎃로울러 4 : 와인더DESCRIPTION OF SYMBOLS 1 Spinner detention 2: The 1st high roller 3: The 2nd high roller 4: Winder
이와 같은 과제들을 달성하기 위한 본 발명의 경편용 해도형 복합섬유의 제조방법은 알칼리 이용해성의 공중합 폴리에스테르를 해성분으로 사용하고 통상의 폴리에스테르를 도성분으로 사용하여 방사 직접 연신 방식으로 50∼90데니어의 경편용 해도형 복합섬유를 제조함에 있어서, 아래 조건을 동시에 충족시킴을 특징으로 한다.The method for producing warp island-in-the-sea composite fiber of the present invention for achieving the above problems is 50 ~ 90 by the direct stretching method using an alkali-soluble copolyester as a sea component and a conventional polyester as a island component In manufacturing the denier warp island-like composite fiber, it is characterized by satisfying the following conditions simultaneously.
- 아 래 --Below-
·제1고뎃로울러의 속도(V1) : 1,000m/분∼3,000m/분Speed of the first high roller (V 1 ): 1,000 m / min to 3,000 m / min
·제2고뎃로울러의 속도(V2) : 4,000m/분∼6,000m/분Speed of the second high roller (V 2 ): 4,000m / min to 6,000m / min
·제1고뎃로울러 상의 원사모듈러스 : 5~35g/dYarn modulus on the first high roller: 5 ~ 35g / d
·제2고뎃로울러 상의 원사결정화도 : 25∼45%Yarn crystallinity on the second high roller: 25 to 45%
이하 본 발명을 상세하게 설명한다.Hereinafter, the present invention will be described in detail.
먼저, 본 발명에서는 알칼리 이용해성인 공중합 폴리에스테르를 해성분으로 사용하고, 통상의 폴리에스테르를 도성분으로 사용하여, 이들을 통상의 해도형 복합방사구금(1)으로 복합방사한다. 이때 해성분으로는 폴리에틸렌테레프탈레이트에 DMIS를 3∼15몰% 공중합 하고, 여기에 다시 수평균 분자량이 8,000 이상인 폴리에틸렌글리콜 4∼20중량%를 첨가한 공중합 폴리에스테르 등을 사용한다.First, in the present invention, alkali-soluble co-polyester is used as a sea component, and ordinary polyester is used as a island component, and these are combined-spun into a conventional island-in-the-sea composite spinneret 1. At this time, 3-15 mol% of DMIS is copolymerized with polyethylene terephthalate, and copolymerized polyester etc. which added 4-20 weight% of polyethyleneglycols whose number average molecular weight is 8,000 or more are used here.
계속해서 본 발명은 방사된 원사를 제1고뎃로울러(2) 및 제2고뎃로울러(3)를 통과시키면서 연신하고, 와인더(4)로 권취하여 해도형 복합섬유를 제조한다. 다시말해 본 발명은 방사와 연신을 동일공정에서 실시하는 방사 직접 연신 공법으로 제조한다. 이때 제1고뎃로울러의 속도(V1)는 1,000∼3,000m/분으로, 제2고뎃로울러의 속도(V2)를 4,000m/분∼6,000m/분으로 설정한다. 제1고뎃로울러(2) 및 제2고뎃로울러(3)의 속도가 상기 범위보다 낮은 경우에는 원사의 충분한 배향결정이 이루어지지 않아 강도는 낮고 신도는 높은 원사가 제조된다. 그 결과 기모시 균일성이 저하되고 감량시 감량편차가 심해 경편용 원사로 사용이 곤란하게 되는 문제가 발생된다. 반면에 상기 범위보다 높은 경우에는 원사의 복굴절율 및 밀도가 급격하게 저하되어 경편작업성 및 후가공 공정성이 저하되는 문제가 발생된다.Subsequently, the present invention draws the spun yarn while passing through the first go roller 2 and the second go roller 3, and winds it up with a winder 4 to produce an island-in-the-sea composite fiber. In other words, the present invention is produced by the spinning direct stretching method in which spinning and stretching are performed in the same process. At this time, the speed V 1 of the first high roller is set at 1,000 to 3,000 m / min, and the speed V 2 of the second high roller is set at 4,000 m / min to 6,000 m / min. When the speeds of the first high roller 2 and the second high roller 3 are lower than the above ranges, sufficient alignment of the yarn is not achieved, so that a yarn of low strength and high elongation is produced. As a result, there is a problem that the uniformity at the time of raising and the weight loss during the loss are severe, making it difficult to use as a warp knitting yarn. On the other hand, if it is higher than the above range, the birefringence and density of the yarn are sharply lowered, which causes a problem that warp knitting workability and post processing fairness are lowered.
또한 제사공정의 각 단계(위치)에서의 원사물성을 아래와 같이 조절하는 것을 특징으로 한다.In addition, it is characterized in that the yarn physical properties at each step (position) of the spinning process is adjusted as follows.
먼저 제1고뎃로울러 상의 원사모듈러스, 다시말해 제1고뎃로울러를 통과하는 원사의 모듈러스는 5~35g/d가 되도록 제조조건을 설정한다. 만약 상기 범위를 벗어나는 경우에는 연신구간 내에서 원사의 모듈러스, 밀도 및 배향도가 급격하게저하되어 연신공정이 매우 곤란하게 되거나, 경편용 원사로는 부적합한 문제가 발생된다.First, the manufacturing conditions are set such that the yarn modulus on the first high roller, that is, the yarn modulus passing through the first high roller, is 5 to 35 g / d. If it is out of the above range, the modulus, density and orientation of the yarn are drastically lowered in the drawing section, so that the drawing process becomes very difficult, or is unsuitable as warp yarn.
또한 제2고뎃로울러 상의 원사결정화도는 25∼45%가 되도록 제조조건을 설정한다. 만약 상기 범위보다 낮은 경우에는 연신구간 내에서 너무 과도한 응력이 걸려 사절 등으로 연신공정이 곤란해지며 원사물성이 저하되고, 상기 범위보다 높은 경우에는 필라멘트가 스티프(Stiff)해져 경편용 원사로 부적합한 문제가 발생된다.In addition, the manufacturing conditions are set so that the degree of yarn crystallization on the second high roller phase is 25 to 45%. If it is lower than the above range, too much stress is applied in the drawing section, so that the drawing process is difficult due to trimming, etc., and the yarn physical property is lowered. If it is higher than the above range, the filament is stiff and is not suitable as a warp yarn. Is generated.
또한 구금직하에서의 원사 복굴절율(Δn)은 0.001 이하가 되도록 하는 것이 더욱 바람직 하다. 구금직하에서의 원사 복굴절율이 상기 범위를 초과하는 경우에는 필라멘트가 고화결정화되는 위치가 구금면과 점차 가까워져 필라멘트에 가해지는 응력이 너무 증가하게 된다. 그 결과 사절 등의 문제가 발생된다.Further, it is more preferable that the yarn birefringence Δn under the detention becomes 0.001 or less. If the yarn birefringence under the crest exceeds the above range, the position at which the filament solidifies crystallizes closer to the surface and the stress applied to the filament increases too much. As a result, problems such as trimming occur.
제1고뎃로울러 상의 원사 모듈러스는 캡쳐를 사용하여 방사중인 사도상 원사를 제1고뎃로울러 후단부에서 절단하는 것과 거의 동시에 제1고뎃로울러 선단부에서 절단한 다음, 제1고뎃로울러 표면상에 권사된 필라멘트를 절단 즉시 샘플로 채취하여 후술하는 방법으로 원사 모듈러스를 측정한 값이다. 더욱 구체적으로 샘플 채취시에는 제1고뎃로울러에 권사된 필라멘트층 중에서 표면에 위치하는 필라멘트를 채취하며, 제1고뎃로울러 온도에 의해 원사물성이 변하는 것을 방지하기 위해 절단 즉시 채취 한다.The yarn modulus on the first roller is cut at the front end of the first roller and then wound on the surface of the first roller, almost simultaneously with the capture of the spinning aspirated yarn at the rear end using capture. It is a value obtained by taking a sample immediately after cutting and measuring the yarn modulus by the method described below. More specifically, during sampling, the filament located on the surface of the filament layer wound on the first roller is collected, and immediately cut to prevent the change of yarn properties by the temperature of the first roller.
제2고뎃로울러 상의 원사 결정화도는 캡쳐를 사용하여 방사중인 사도상 원사를 제2고뎃로울러의 선단부와 후단부에서 동시에 절단하고, 제2고뎃로울러 표면상에 권사된 필라멘트를 절단 즉시 샘플로 채취하여 후술하는 방법으로 원사 결정화도를 측정한 값이다. 원사 절단 즉시 샘플을 채취하지 않으면, 제2고뎃로울러 온도에 의해 원사물성이 변하게 될 수 있다.The degree of crystallinity of the yarn on the second roller is cut at the same time as the yarns of the yarns being spun at the front and rear of the second roller by using a capture, and the sample of the filament wound on the surface of the second roller is immediately cut. It is the value which measured the degree of crystallinity of yarn by the method. If the sample is not taken immediately after the yarn is cut, the yarn properties may change with the temperature of the second roller.
구금직하에서 원사 복굴절율은 방사중인 원사의 고화점에서부터 길이가 1m인 캡쳐를 사용하여 시료를 채취한 다음 후술하는 방법으로 복굴절율을 측정한다. 상기 복굴절율은 채취한 해도형 복합섬유(샘플)을 1% NaOH 용액에서 30분간 처리하여 이들중 해성분을 용출한 후 후술하는 방법과 같이 편광현미경으로 측정한 값이다.Yarn birefringence under detention is measured using a capture of 1 m in length from the spinning point of the spinning yarn, and then the birefringence is measured by the method described below. The birefringence is a value obtained by treating the sampled island-in-the-sea composite fiber (sample) in a 1% NaOH solution for 30 minutes to elute the sea component among them and measuring it with a polarizing microscope as described below.
본 발명에서는 상기와 같은 방법으로 해성분 용출전의 단사섬도가 2∼4데니어, 해성분 용출후의 단사섬도가 0.001∼0.3데니어인 총섬도 50∼90데니어의 경편용 해도형 복합섬유를 제조한다. 본 발명의 방법으로 제조한 해도형 복합섬유는 해성분 용출후의 원사 모듈러스가 25∼60g/d, 신도가 40∼60%, 강도가 2.0∼4.0g/d, 결정배향도(Fc)가 0.80∼0.95이다. 본 발명의 방법으로 제조한 해도형 복합섬유로 경편지를 제편한 다음, 알칼리 용액으로 해성분을 용출하고, 기모하여 기모 경편지를 제조한다. 해성분의 용출은 해도형 복합섬유를 1% 농도의 수산화나트륨 용액(욕비 = 10:1)에서 95℃로 30분간 처리하여 실시한다.In the present invention, a warp island-like composite fiber having a total fineness of 50 to 90 denier having a single yarn fineness of 2 to 4 deniers prior to sea component elution and a 0.001 to 0.3 denier single yarn fineness after sea component elution is produced. The island-in-the-sea composite fiber produced by the method of the present invention has a yarn modulus of 25 to 60 g / d, an elongation of 40 to 60%, an intensity of 2.0 to 4.0 g / d, and a crystal orientation (Fc) of 0.80 to 0.95 after sea component elution. to be. After knitting the warp knitted paper with the island-in-the-sea composite fiber prepared by the method of the present invention, the sea component is eluted with an alkaline solution and brushed to prepare a brushed warp knit. The dissolution of the sea component is carried out by treating the island-in-sea composite fiber with 95 ° C. for 30 minutes in a 1% sodium hydroxide solution (bath ratio = 10: 1).
본 발명의 방법으로 제조한 해도형 복합섬유는 해성분의 용출성 및 원사물성 특성 등에 기인하여 상기 해성분 용출공정이나 기모공정에서 원사 물성 저하가 최소화 된다. 그 결과 기모성이 향상되며, 최종제품인 경편지의 외관 및 촉감이 우수하게 된다.The island-in-the-sea composite fiber produced by the method of the present invention is minimized in yarn property degradation during the sea component elution process or brushing process due to the elution property and yarn property characteristics of the sea component. As a result, the raising property is improved, and the appearance and feel of the warp knitted fabric as the final product are excellent.
본 발명에 있어서, 원사물성은 아래와 같이 평가 하였다.In the present invention, the yarn physical properties were evaluated as follows.
·강도/신도/모듈러스: 인스트롱 회사의 인장시험기로 50회 측정(시료길이 : 5cm, 인장속도 : 30cm/분)하여 평균값을 구한다. 여기서 모듈러스는 초기 모듈러스를 의미한다. Strength / Elongation / Modulus : The average value is obtained by measuring 50 times (Instrument Length: 5cm, Tensile Speed: 30cm / min) with Instron Company's tensile tester. Here modulus means initial modulus.
·밀도(ρ): 해도형 복합섬유를 노말헵탄과 카본테트라클로라이드 혼합용매로 구성된 밀도계(일본 시바야마 회사제품, 모델명 : Model SS)에 투입하여 해성분과 도성분이 통합된 벌크한 상태의 밀도를 측정한다. Density (ρ) : The island-in-the-sea composite fiber is introduced into a density meter composed of a mixed solvent of normal heptane and carbon tetrachloride (Shibayama, Japan, Model SS). Measure
·결정화도[Xc(%)]: 상기의 밀도(ρ)값을 바탕으로 이론적인 폴리에스테르의 완전 결정영역의 밀도값(ρc=1.457g/㎤)과 완전 비결정영역의 밀도값(1.336g/㎤)을 이용하여 아래 공식으로 구한다. Crystallinity [Xc (%)] : Based on the above density (ρ) value, the theoretical density of the complete crystal region of polyester (ρ c = 1.457 g / cm 3) and the density value of the complete amorphous region (1.336 g / Using cm 3)
·복굴절율(Δn): 간섭현미경(독일 칼 자이스 회사제품, 모델명 : JENAPOL -U INTERPHAKO)으로 측정 하였다. 복굴절율은 아래 공식으로 구한다.It was measured by: (JENAPOL -U INTERPHAKO German company Carl Zeiss product, model), birefringence (Δn) interference microscope. The birefringence is calculated by the formula below.
여기서, R은 보상지연 값(Compensator retardation) 이고, S는 석영플레이트의 지연값(Retardation of quartz shim) 이고, D는 파이버 직경(Fiber Diameter) 이다. 또한 R과 S의 단위는 nm이고 D의 단위는 ㎛ 이다.Where R is the compensator retardation, S is the retardation of quartz shim, and D is the fiber diameter. In addition, the units of R and S are nm and the units of D are μm.
·결정배향도(Fc): X-선 회절분석기로 결정의 (010)면과 (100)면에 대해 방위각 주사(azimuthal scanning)를 행하여 결정배향의 특성을 나타내는 피크(peak)의 반가폭(FWHM, Full width at half-maximum intensity)을 측정하여 도성분의 결정배향도(Fc)를 계산하였다. 단, 해성분은 완전 무정형 상태이므로 방위각 주사에 의하여 나타난 피크를 전부 도성분의 결정면에 의한 피크로 간주한다. 반가폭(FWHM)으로부터 결정배향도(Fc)를 계산한 식은 다음과 같다. Crystal orientation (Fc) : The half width of the peak (FWHM, which shows the characteristics of crystal orientation by performing azimuthal scanning on the (010) and (100) planes of the crystal by using an X-ray diffractometer) The crystal orientation (Fc) of the island components was calculated by measuring the full width at half-maximum intensity. However, since the sea component is completely amorphous, all peaks resulting from the azimuth scan are regarded as peaks due to the crystal plane of the island component. The equation for calculating the crystal orientation (Fc) from the full width (FWHM) is as follows.
이하 실시예 및 비교실시예를 통하여 본 발명을 더욱 구체적으로 살펴 본다. 그러나 본 발명이 하기 실시예에만 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples. However, the present invention is not limited only to the following examples.
실시예 1Example 1
디메틸이소프탈레이트술포네이트 나트륨이 4몰% 공중합 되어 있는 공중합 폴리에스테르에 수평균 분자량이 8,500인 폴리에틸렌글리콜 8중량%를 블랜딩하여 알칼리 이용해성 폴리머를 제조한다. 제조된 상기 알칼리 이용해성 폴리머를 해성분으로 사용하고, 고유점도가 0.65인 폴리에틸렌테레프탈레이트를 도성분으로 사용하여, 이들을 288℃에서 도성분 수가 36개인 해도형 복합방사 구금을 통해 방사한다. 계속해서 방사된 원사를 속도가 1,500m/분인 80℃의 제1고뎃로울러와 속도가 4,200m/분인 125℃의 제2고뎃로울러 사이에서 연신하고, 계속해서 4,300m/분의 권취속도로 권취하여 75데니어 24필라멘트의 해도형 복합섬유를 제조한다. 이때 구금직하에서의 원사복굴절율은 0.0009, 제1고뎃로울러 상의 원사모듈러스는 18.1g/d, 제2고뎃로울러 상의 원사결정화도는 33.24%가 되도록 제조조건을 설정 하였다. 이와 같이 제조한 해도형 복합섬유를 95℃의 1% NaOH 용액에서 해도형복합섬유를 30분 동안 처리하여 해성분을 용출한 다음, 해성분 용출후의 원사물성을 앞에서 설명한 방법으로 평가한 결과는 표 2와 같다.An alkali-soluble polymer is prepared by blending 8% by weight of polyethylene glycol having a number average molecular weight of 8,500 to a copolymerized polyester having 4 mol% of dimethylisophthalatesulfonate sodium copolymerized. Using the prepared alkali-soluble polymer as a sea component, and polyethylene terephthalate having an intrinsic viscosity of 0.65 as a island component, they are spun through a island-in-the-sea composite spinneret having 36 island components at 288 ° C. The spun yarn was then drawn between a first high roller at 80 ° C. with a speed of 1,500 m / min and a second high roller at 125 ° C. with a speed of 4,200 m / min, and then wound at a winding speed of 4,300 m / min. A sea island type composite fiber of 75 denier 24 filaments is prepared. At this time, the manufacturing conditions were set such that the birefringence of the yarn under detention was 0.0009, the yarn modulus on the first high roller was 18.1 g / d, and the crystallinity on the second high roller was 33.24%. The islands-in-sea composite fiber prepared in this way was treated with island-in-sea composite fiber for 30 minutes in a 1% NaOH solution at 95 ° C. to elute the sea component, and then the raw material properties after sea component elution were evaluated by the method described above. Same as 2.
실시예 2 ∼ 실시예 3 및 비교실시예 1 ∼ 비교실시예 2Example 2-Example 3 and Comparative Example 1-Comparative Example 2
제1고뎃로울러 속도 등의 제조조건을 표 1과 같이 변경한 것을 제외하고는 실시예 1과 동일한 공정 및 조건으로 75데니어 24필라멘트의 해도형 복합섬유를 제조한다. 이와 같이 제조한 해도형 복합섬유를 95℃의 1% NaOH 용액에서 해도형 복합섬유를 30분 동안 처리하여 해성분을 용출한 다음, 해성분 용출후 원사물성을 앞에서 설명한 방법으로 평가한 결과는 표 2와 같다.The island-like composite fibers of 75 denier 24 filaments were manufactured under the same process and conditions as in Example 1 except that the manufacturing conditions such as the first high roller speed were changed as shown in Table 1. The islands-in-sea composite fiber prepared in this way was treated with island-in-sea composite fiber in 95% 1% NaOH solution for 30 minutes to elute the sea component, and then the raw material properties were evaluated by the method described above. Same as 2.
본 발명의 방법으로 제조된 경편용 해도형 복합섬유는 해성분 용출 및 기모공정에서 원사 물성 손상이 최소화 된다. 그 결과 경편지 제조시 기모성이 우수하게 되어 촉감 및 외관이 우수한 경편지를 제조 할 수 있다. 이와 같은 효과로 인해 본 발명의 방법으로 제조된 해도형 복합섬유는 기모 경편지 제조에 특히 유용하다.The island-in-the-sea island composite fiber for warp knitting produced by the method of the present invention minimizes damage to yarn physical properties in seawater dissolution and raising processes. As a result, it is excellent in brushing when manufacturing the warp knitted paper, it is possible to manufacture a warp knitted paper with excellent feel and appearance. Due to this effect, the island-in-the-sea composite fiber produced by the method of the present invention is particularly useful for producing brushed warp knits.
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KR900004975A (en) * | 1988-09-05 | 1990-04-13 | 김상응 | Method of manufacturing island-in-the-sea composite fiber |
JPH0359111A (en) * | 1989-07-25 | 1991-03-14 | Unitika Ltd | Polyester fiber and production thereof |
JPH03124878A (en) * | 1989-10-09 | 1991-05-28 | Toray Ind Inc | Production of fabric made of polyamide-polyester conjugated fiber |
KR910020207A (en) * | 1990-05-31 | 1991-12-19 | 이승동 | Manufacturing method of island-in-the-sea composite fiber |
JPH07292516A (en) * | 1994-04-15 | 1995-11-07 | Mitsubishi Rayon Co Ltd | Polyester sheath core composite fiber and method for producing the same |
KR19980050087A (en) * | 1996-12-20 | 1998-09-15 | 이명환 | Manufacturing method of polyester islands-in-the-sea composite fiber |
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KR900004975A (en) * | 1988-09-05 | 1990-04-13 | 김상응 | Method of manufacturing island-in-the-sea composite fiber |
JPH0359111A (en) * | 1989-07-25 | 1991-03-14 | Unitika Ltd | Polyester fiber and production thereof |
JPH03124878A (en) * | 1989-10-09 | 1991-05-28 | Toray Ind Inc | Production of fabric made of polyamide-polyester conjugated fiber |
KR910020207A (en) * | 1990-05-31 | 1991-12-19 | 이승동 | Manufacturing method of island-in-the-sea composite fiber |
JPH07292516A (en) * | 1994-04-15 | 1995-11-07 | Mitsubishi Rayon Co Ltd | Polyester sheath core composite fiber and method for producing the same |
KR19980050087A (en) * | 1996-12-20 | 1998-09-15 | 이명환 | Manufacturing method of polyester islands-in-the-sea composite fiber |
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