JP3279529B2 - Split type composite yarn with excellent antistatic performance - Google Patents
Split type composite yarn with excellent antistatic performanceInfo
- Publication number
- JP3279529B2 JP3279529B2 JP27850598A JP27850598A JP3279529B2 JP 3279529 B2 JP3279529 B2 JP 3279529B2 JP 27850598 A JP27850598 A JP 27850598A JP 27850598 A JP27850598 A JP 27850598A JP 3279529 B2 JP3279529 B2 JP 3279529B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- polyester
- formula
- antistatic agent
- composite yarn
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000002131 composite material Substances 0.000 title claims description 26
- 229920000728 polyester Polymers 0.000 claims description 34
- 239000002216 antistatic agent Substances 0.000 claims description 27
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 6
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000013256 coordination polymer Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 230000003068 static effect Effects 0.000 description 7
- 125000002091 cationic group Chemical group 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 230000005611 electricity Effects 0.000 description 6
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 229920001410 Microfiber Polymers 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- QPKOBORKPHRBPS-UHFFFAOYSA-N bis(2-hydroxyethyl) terephthalate Chemical compound OCCOC(=O)C1=CC=C(C(=O)OCCO)C=C1 QPKOBORKPHRBPS-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- IBBQVGDGTMTZRA-UHFFFAOYSA-N sodium;2-sulfobenzene-1,3-dicarboxylic acid Chemical compound [Na].OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O IBBQVGDGTMTZRA-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Multicomponent Fibers (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、静電気の発生が抑制さ
れた、扱い易い極細繊維製造用の割繊型複合糸に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a split type composite yarn for producing ultrafine fibers which is easy to handle and suppresses generation of static electricity.
【0002】[0002]
【従来の技術】極細繊維製造用の割繊型複合糸は、単一
フィラメント内で第一成分が第二成分によって少なくと
も3個以上のセグメントに分離されているマルチセグメ
ントフィラメントであって、二成分間の親和性、溶解
性、分解性尚の違いによって、第二成分Bを化学的に溶
解又は分解除去したり、又は機械的に二成分間を分離し
て、セグメントを分割し、極細繊維に形成できるもので
ある。2. Description of the Related Art Split-split composite yarns for producing ultrafine fibers are multi-segment filaments in which a first component is separated into at least three or more segments by a second component in a single filament. The affinity, solubility, and degradability of the second component B are chemically dissolved or decomposed and removed, or the two components are mechanically separated from each other depending on the difference between the two components. It can be formed.
【0003】その製法は、種々検討されており、例え
ば、特公昭48−28005号公報、特公昭61−34
278号公報、特開平6−306734号公報等に開示
されており、ナイロンとポリエステルからなる割繊型複
合糸も知られているが、割繊型複合糸は、割繊して極細
繊維となるため、静電気の発生が大きく、扱い難く、ま
た、染色後の発色性や堅牢度にも問題があった。Various methods have been studied for the production method, for example, JP-B-48-28005 and JP-B-61-34.
No. 278, Japanese Unexamined Patent Publication No. 6-306734 and the like, split type composite yarns made of nylon and polyester are also known, but split type composite yarns split into ultrafine fibers. As a result, the generation of static electricity is large and it is difficult to handle, and there are also problems in the color developability and fastness after dyeing.
【0004】そこで、ポリエステル成分に制電剤を入れ
て使用する試みもあるが、通常のポリエステル成分に市
販の制電剤を混入しても、十分な制電効果は得られず、
また、染色後の発色性等の問題は解決されなかった。There is an attempt to use an antistatic agent in the polyester component. However, even if a commercially available antistatic agent is mixed in the ordinary polyester component, a sufficient antistatic effect cannot be obtained.
In addition, problems such as color development after dyeing were not solved.
【0005】[0005]
【発明が解決しようとする課題】本発明は、ナイロンと
ポリエステルからなる割繊型複合糸を、より制電性に富
んだ扱い易いものとし、かつ染色後の発色性も改善する
ことを課題とする。SUMMARY OF THE INVENTION It is an object of the present invention to make split-split composite yarns made of nylon and polyester more antistatic and easy to handle, and to improve the coloring properties after dyeing. I do.
【0006】[0006]
【課題を解決するための手段】本発明では、ポリエステ
ル成分にカチオン型ポリエステルを使用し、制電剤に特
殊なポリエステル系制電剤を使用することにより、上記
課題を解決した。即ち、本発明の割繊型複合糸は、ポリ
アミド成分Aと、ポリエステル中に含有する酸成分に対
し、0.5〜2.0モル%の金属スルホネート基含有イソフ
タル酸を含有する繊維形成性ポリエステル成分Bからな
る複合糸で、一方の成分A又はBが、他方の成分B又は
Aを少なくとも2分割するように、前記複合糸の横断面
に放射状に位置するものであって、上記成分B中に、ポ
リアルキレングリコール及びイオン性制電剤からなるポ
リエステル系制電剤が、前記複合糸の長手方向に、筋状
に前記成分Bの重量に対して0.1〜3.0重量%の割合で
含有されていることを特徴とする。In the present invention, the above-mentioned problems have been solved by using a cationic polyester as a polyester component and using a special polyester-based antistatic agent as an antistatic agent. That is, the splitting type composite yarn of the present invention is a fiber-forming polyester containing 0.5 to 2.0 mol% of a metal sulfonate group-containing isophthalic acid with respect to a polyamide component A and an acid component contained in the polyester. In the composite yarn comprising the component B, one component A or B is located radially on the cross section of the composite yarn so that the other component B or A divides the other component B or A into at least two. A polyester-based antistatic agent comprising a polyalkylene glycol and an ionic antistatic agent, in a longitudinal direction of the composite yarn, in a ratio of 0.1 to 3.0% by weight with respect to the weight of the component B in the form of a stripe. It is characterized by being contained in.
【0007】ここに「長手方向に、筋状に」とは、必ず
しも長手方向に一本の筋となっていなくてもよく、ポリ
エステル系制電剤が0.1〜3.0重量%の添加率で十分な
効果が得られるように長手方向に連続して存在すればよ
い。ポリエステル系制電剤がポリマー全体に均一に混合
されてしまうと上記添加率では、十分な効果を得ること
ができないので、例えば、当該制電剤をポリエステル成
分Bに圧入した後に、L/D=1.5のスタティックミキ
サーを5から11ケ通過させて混合するのが好ましい。[0007] Here, "in the longitudinal direction, in the form of a streak" means that it is not always necessary to form one streak in the longitudinal direction, and the polyester-based antistatic agent is added in an amount of 0.1 to 3.0% by weight. It suffices if it exists continuously in the longitudinal direction so that a sufficient effect can be obtained at a rate. If the polyester-based antistatic agent is uniformly mixed into the entire polymer, the above addition rate cannot provide a sufficient effect. For example, after the antistatic agent is pressed into the polyester component B, L / D = Preferably, the mixture is passed through 5 to 11 static mixers and mixed.
【0008】上記制電剤としては、例えば式1で示され
るイオン性制電剤を15〜40重量%含有し、平均分子
量が1000〜10000の範囲にある式2のポリアル
キレングリコールとテレフタル酸からなるポリエステル
化合物を使用するのが好ましい。 〔式1〕 RSO3 - M+ 〔式2〕 HO−(Cn H2nO)m −OH (但し、式1のRはアルキル基、アリール基、アルアル
キル基又はアルキルアリール基を、MはLi、Na又は
Kを示し、式2のnは1〜4の整数を、mは式2のポリ
アルキレングリコールの平均分子量が1000〜100
00になる数を示す。)As the above-mentioned antistatic agent, for example, a polyalkylene glycol of the formula 2 containing 15 to 40% by weight of an ionic antistatic agent represented by the formula 1 and having an average molecular weight in the range of 1,000 to 10,000, and terephthalic acid are used. It is preferable to use a polyester compound represented by the following formula: [Equation 1] RSO 3 - M + [Formula 2] HO- (C n H 2n O) m -OH ( where, R represents an alkyl group of formula 1, an aryl group, an aralkyl group or alkylaryl group, M is Represents Li, Na or K, n in Formula 2 is an integer of 1 to 4, and m is an average molecular weight of the polyalkylene glycol of Formula 2 of 1000 to 100.
Indicates a number that becomes 00. )
【0009】なお、式1の制電剤としては、通常、Rと
して、例えば炭素数10〜20のアルキル基、アリール
基、アルアルキル基又はアルキルアリール基を有するも
のを使用するのが好ましい。As the antistatic agent of the formula 1, it is usually preferable to use, for example, R having an alkyl group, an aryl group, an aralkyl group or an alkylaryl group having 10 to 20 carbon atoms.
【0010】また、成分Bとしては、特に0.5〜2.0モ
ル%の金属スルホネート基含有イソフタル酸を含有する
繊維形成性ポリエステルを使用するのが好ましい。金属
スルホネート基含有イソフタル酸の量が0.5モル%未満
では、制電性、染色性共に十分な効果が得られず、2.0
モル%を越えると、ポリアミド成分のカチオン基との電
気的な親和性が増加するために、割繊し難くなってしま
う。また、上記繊維形成性ポリエステルとは、具体的に
は、ポリエチレンテレフタレート、ポリブチレンテレフ
タレート、ポリエチレンナフタレート等、ポリアミドと
の複合形態で繊維形成能あるポリエステルポリマーを示
す。As the component B, it is particularly preferable to use a fiber-forming polyester containing 0.5 to 2.0 mol% of a metal sulfonate group-containing isophthalic acid. If the amount of isophthalic acid containing a metal sulfonate group is less than 0.5 mol%, sufficient antistatic and dyeing effects cannot be obtained, and 2.0
If it exceeds mol%, the electric affinity with the cationic group of the polyamide component increases, so that the splitting becomes difficult. Further, the fiber-forming polyester specifically refers to a polyester polymer having a fiber-forming ability in a composite form with a polyamide, such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate.
【0011】なお、これに混入する上記制電剤の量は、
成分Bの重量に対して0.1〜3.0重量%であるのが好ま
しく、0.5〜1.5重量%であるのが特に好ましい。[0011] The amount of the antistatic agent to be mixed therein is as follows:
It is preferably from 0.1 to 3.0% by weight, particularly preferably from 0.5 to 1.5% by weight, based on the weight of component B.
【0012】かかる本発明の複合糸は、成分A─ポリア
ミド─のカチオン基及び成分B─カチオン性ポリエステ
ル─のアニオン基により、静電気の発生が抑制され、ま
た、イオン性制電剤を含む特殊なポリエステル系制電剤
が、繊維の長手方向に筋状に存在するため、発生した静
電気が直に消失される(電圧の半減期が短い)という効
果を有するものであり、複合糸を構成するポリマー全体
に電荷を有しているため、静電気の繊維表面からの消失
も早く、非常に扱い易いものとなる。In the composite yarn of the present invention, the generation of static electricity is suppressed by the cationic group of component A (polyamide) and the anionic group of component B (cationic polyester), and the special yarn containing an ionic antistatic agent is used. Since the polyester-based antistatic agent is present in a streak shape in the longitudinal direction of the fiber, the generated static electricity is immediately eliminated (the half-life of the voltage is short). Since it has an electric charge as a whole, static electricity quickly disappears from the fiber surface, and it is very easy to handle.
【0013】[0013]
【発明の実施の形態】次に、本発明の実施例を示すが、
実施例において部及び%とあるのは、特に断らない限
り、重量部及び重量%を示す 実施例1(ポリエステル系制電剤の製造方法) 平均分子量8000のポリエチレングリコール73.6
部、酸化防止剤(日本チバガイギー社製のイルガノック
ス1010)0.1部、重縮合触媒(三酸化アンチモン)
0.037部、ビスヒドロキシエチルテレフタレート(以
下BHETと称す)8.8部及びドデシルベンゼンスルホ
ン酸ナトリムの65%水混合物30.8部を、それぞれ重
縮合反応器に投入して、窒素気流中、常圧下、攪拌混合
しつつ昇温した。160℃で6時間、その後240℃×
6時間かけて、十分に水分を除去した後に、240℃に
維持したまま、2時間かけて760mmHgから1mmHgまで
減圧した。更に、250℃まで昇温して、3時間1mmHg
以下を保持し、溶融粘度を上昇させて相対粘度3.00の
ポリエステル系制電剤100部を得た。Next, an embodiment of the present invention will be described.
In the examples, parts and% indicate parts by weight and% by weight, respectively, unless otherwise specified. Example 1 (Method for producing polyester-based antistatic agent) Polyethylene glycol 73.6 having an average molecular weight of 8000
Parts, 0.1 part of antioxidant (Irganox 1010 manufactured by Ciba-Geigy Japan), polycondensation catalyst (antimony trioxide)
0.037 parts, 8.8 parts of bishydroxyethyl terephthalate (hereinafter referred to as BHET) and 30.8 parts of a 65% aqueous mixture of sodium dodecylbenzenesulfonate were each charged into a polycondensation reactor, and charged in a nitrogen stream. The temperature was raised while stirring and mixing under normal pressure. 6 hours at 160 ° C, then 240 ° C
After sufficiently removing water over 6 hours, the pressure was reduced from 760 mmHg to 1 mmHg over 2 hours while maintaining the temperature at 240 ° C. Further, the temperature was raised to 250 ° C. and 1 mmHg for 3 hours.
While maintaining the following conditions, the melt viscosity was increased to obtain 100 parts of a polyester-based antistatic agent having a relative viscosity of 3.00.
【0014】実施例2 常法に従い、全酸成分に対して1.5モル%のソジウムス
ルホイソフタル酸成分を含有する、固有粘度が0.57の
共重合ポリエチレンテレフタレート(以下、CPと称
す)─成分B─を得た。CPと相対粘度が2.70の6−
ナイロン(以下、NPと称す)─成分A−を用いて、図
1に示される断面形状の糸に、従来公知の複合紡糸方法
に従い、CPとNPの複合比(重合比)が2:1の複合
マルチフィラメント(50デニール25フィラメント)
を紡糸温度290℃、捲取速度1000m/分で紡糸し
た。その際、CP中に、CP成分に対して0.9重量%の
割合で実施例1のポリエステル系制電剤を、フィラメン
トの長手方向に筋状となるように圧入した。得られた未
延伸糸を、速度800m/分、85℃のローラーヒータ
ー及び150℃のプレートヒーターで熱処理をしつつ延
伸倍率3.232で延伸して、50デニール25フィラメ
ントの複合マルチフィラメントを得た。Example 2 A copolymerized polyethylene terephthalate (hereinafter referred to as CP) having an intrinsic viscosity of 0.57 and containing 1.5 mol% of sodium sulfoisophthalic acid component based on the total acid component, according to a conventional method. {Component B} was obtained. 6 having a relative viscosity of 2.70 with CP
Using nylon (hereinafter referred to as NP) {component A-}, a yarn having the cross-sectional shape shown in FIG. 1 was mixed with a yarn having a composite ratio (polymerization ratio) of CP and NP of 2: 1 according to a conventionally known composite spinning method. Composite multifilament (50 denier 25 filament)
Was spun at a spinning temperature of 290 ° C. and a winding speed of 1000 m / min. At that time, the polyester-based antistatic agent of Example 1 was pressed into the CP at a ratio of 0.9% by weight with respect to the CP component so as to form a streak in the longitudinal direction of the filament. The obtained undrawn yarn was drawn at a draw ratio of 3.232 while being heat-treated with a roller heater at 85 ° C. and a plate heater at 150 ° C. at a speed of 800 m / min to obtain a composite multifilament of 50 denier and 25 filaments. .
【0015】比較例3 CPとNPを用いて、実施例2と同様に複合マルチフィ
ラメントを紡糸した。ただし、ポリエステル系制電剤は
圧入しなかった。Comparative Example 3 Using CP and NP, a composite multifilament was spun in the same manner as in Example 2. However, the polyester antistatic agent was not injected.
【0016】比較例4 CPの代わりに固有粘度0.64のポリエチレンテレフタ
レート(以下、PETと称する)を用いて、実施例2と
同様に、ポリエステル系制電剤を圧入して複合マルチフ
ィラメントを得た。Comparative Example 4 Polyethylene terephthalate (hereinafter referred to as PET) having an intrinsic viscosity of 0.64 was used in place of CP, and a polyester-based antistatic agent was pressed into it to obtain a composite multifilament as in Example 2. Was.
【0017】比較例5 比較例4と同様の方法を、ポリエステル系制電剤を圧入
せずに実施した。Comparative Example 5 The same method as in Comparative Example 4 was carried out without injecting the polyester antistatic agent.
【0018】制電性能評価方法 1.複合マルチフィラメントの開繊処理 実施例2、比較例3、4で得られた複合マルチフィラメ
ントをそれぞれ、2本合糸にて、筒編み機にて布帛と
し、各布帛を、室温にて、15%のベンジルアルコール
水溶液に10分間浸漬し、NP成分を十分に膨潤させた
後、60℃の温水で、10分間湯洗処理して、室温にて
風乾した。処理後の筒編み布帛は、全て完全にNP成分
とポリエステル成分が分割され割繊されていた。 2.制電性能の評価 上記1で得られた割繊された筒編み布帛を、JIS L
−1094に記載された測定方法の内、帯電圧はB法、
半減期はA法にて、それぞれ測定した。測定結果を表1
に示す。Evaluation method of antistatic performance Opening treatment of composite multifilament The composite multifilaments obtained in Example 2 and Comparative Examples 3 and 4 were each made into a fabric with a double knitting yarn by using a tubular knitting machine. Was immersed in an aqueous benzyl alcohol solution for 10 minutes to sufficiently swell the NP component, then washed with hot water at 60 ° C. for 10 minutes, and air-dried at room temperature. In the tubular knitted fabric after the treatment, the NP component and the polyester component were completely divided and split. 2. Evaluation of antistatic performance The split tubular knitted fabric obtained in 1 above was subjected to JIS L
Of the measurement methods described in -1094, the charged voltage is the B method,
The half-life was measured by the method A, respectively. Table 1 shows the measurement results.
Shown in
【0019】 表1─測定条件:温度20℃、湿度40RH%─ . 実施例2 比較例3 比較例4 比較例5 糸構成 ・ポリアミド成分 NP NP NP NP ・PET成分 CP CP PET PET ・制電剤 0.9w% 無 0.9w% 無 帯電圧(V) 1050 5434 2201 6352 半減期(秒) 9.0 120以上 9.5 120以上Table 1 {Measurement conditions: temperature 20 ° C., humidity 40 RH%}. Example 2 Comparative Example 3 Comparative Example 4 Comparative Example 5 Yarn Configuration • Polyamide component NP NP NP NP • PET component CP CP PET PET • Antistatic agent 0.9 w% no 0.9 w% no charged voltage (V) 1050 5434 2201 6352 Half-life (sec) 9.0 120 or more 9.5 120 or more
【0020】[0020]
【発明の効果】本発明の割繊型複合糸は、カチオン型ポ
リエステルの使用により、染色後の発色性等にも優れ、
しかも、ナイロンとカチオン型ポリエステルの相反する
イオン性、及びポリエステル成分が特殊なポリエステル
系制電剤を繊維の長手方向に筋状に含有することによ
り、非常に制電性に富み、また静電気が発生しても直に
消失するという効果を有する。EFFECT OF THE INVENTION The split type composite yarn of the present invention is excellent in color development after dyeing by using a cationic polyester,
In addition, the opposite ionicity of nylon and cationic polyester, and the polyester component contains a special polyester-based antistatic agent in the form of stripes in the longitudinal direction of the fiber, so it is extremely rich in antistatic properties and generates static electricity. This has the effect of disappearing immediately.
【図1】本発明の実施例における複合糸の断面図であ
る。FIG. 1 is a cross-sectional view of a composite yarn according to an embodiment of the present invention.
A ナイロン B 共重合ポリエチレンテレフタレート A nylon B copolymerized polyethylene terephthalate
フロントページの続き (72)発明者 本田 繁喜 山口県防府市鐘紡町4番1号 カネボウ 合繊株式会社内 (72)発明者 吉田 伸治 福井県鯖江市水落町47字三反田35番1 カネボウ合繊株式会社内 (72)発明者 高瀬 清 大阪府大阪市北区梅田1丁目2番2号 カネボウ合繊株式会社内 (56)参考文献 特開 平9−241927(JP,A) 特開 昭50−107215(JP,A) 特開 平6−341033(JP,A) 特開 昭56−20615(JP,A) 特開 平6−158429(JP,A) (58)調査した分野(Int.Cl.7,DB名) D01F 8/12 D01F 8/14 D01F 6/92 301 - 309 Continued on the front page (72) Inventor Shigeki Honda 4-1 Kanebocho, Hofu City, Yamaguchi Prefecture Kanebo Synthetic Fibers Co., Ltd. (72) Inventor Kiyoshi Takase 1-2-2 Umeda, Kita-ku, Osaka-shi, Osaka Kanebo Synthetic Fiber Co., Ltd. (56) References JP-A-9-241927 (JP, A) JP-A-50-107215 (JP, A) JP-A-6-343033 (JP, A) JP-A-56-20615 (JP, A) JP-A-6-158429 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) ) D01F 8/12 D01F 8/14 D01F 6/92 301-309
Claims (2)
含有する酸成分に対し、0.5〜2.0モル%の金属スルホ
ネート基含有イソフタル酸を含有する繊維形成性ポリエ
ステル成分Bからなる複合糸で、一方の成分A又はB
が、他方の成分B又はAを少なくとも2分割するよう
に、前記複合糸の横断面に放射状に位置するものであっ
て、上記成分B中に、イオン性制電剤とポリアルキレン
グリコールを使用したポリエステル系制電剤が、前記複
合糸の長手方向に、筋状に前記成分Bの重量に対して0.
1〜3.0重量%の割合で含有されていることを特徴とす
る優れた制電性能を有する割繊型複合糸。A composite yarn comprising a polyamide component A and a fiber-forming polyester component B containing isophthalic acid containing a metal sulfonate group in an amount of 0.5 to 2.0 mol% based on an acid component contained in the polyester. , One component A or B
Is located radially on the cross section of the composite yarn so as to divide the other component B or A into at least two. In the component B, an ionic antistatic agent and polyalkylene glycol are used. A polyester-based antistatic agent is streaked in the longitudinal direction of the composite yarn in an amount of 0.2 to the weight of the component B.
Split split type composite yarn having excellent antistatic performance, characterized in that it is contained at a ratio of 1 to 3.0% by weight.
電剤を15〜40重量%含有し、平均分子量が1000
〜10000の範囲にある式2のポリアルキレングリコ
ールとテレフタル酸からなるポリエステル化合物である
ことを特徴とする請求項1記載の割繊型複合糸。 〔式1〕 RSO3 - M+ 〔式2〕 HO−(Cn H2nO)m −OH (但し、式1のRはアルキル基、アリール基、アルアル
キル基又はアルキルアリール基を、MはLi、Na又は
Kを示し、式2のnは1〜4の整数を、mは式2のポリ
アルキレングリコールの平均分子量が1000〜100
00になる数を示す。)2. The antistatic agent contains 15 to 40% by weight of an ionic antistatic agent represented by the formula 1, and has an average molecular weight of 1,000.
2. The split yarn according to claim 1, wherein the split yarn is a polyester compound comprising a polyalkylene glycol of the formula 2 and terephthalic acid in a range of from 1 to 10,000. 3. [Equation 1] RSO 3 - M + [Formula 2] HO- (C n H 2n O) m -OH ( where, R represents an alkyl group of formula 1, an aryl group, an aralkyl group or alkylaryl group, M is Represents Li, Na or K, n in Formula 2 is an integer of 1 to 4, and m is an average molecular weight of the polyalkylene glycol of Formula 2 of 1000 to 100.
Indicates a number that becomes 00. )
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27850598A JP3279529B2 (en) | 1998-09-30 | 1998-09-30 | Split type composite yarn with excellent antistatic performance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27850598A JP3279529B2 (en) | 1998-09-30 | 1998-09-30 | Split type composite yarn with excellent antistatic performance |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000110029A JP2000110029A (en) | 2000-04-18 |
| JP3279529B2 true JP3279529B2 (en) | 2002-04-30 |
Family
ID=17598257
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27850598A Expired - Lifetime JP3279529B2 (en) | 1998-09-30 | 1998-09-30 | Split type composite yarn with excellent antistatic performance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3279529B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008088592A (en) * | 2006-09-29 | 2008-04-17 | Kb Seiren Ltd | Core-sheath type conjugated polyester fiber |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008202194A (en) * | 2007-02-22 | 2008-09-04 | Teijin Cordley Ltd | Ultra fine filament nonwoven fabric and method for producing ultra fine filament nonwoven fabric |
| JP6693562B2 (en) * | 2017-07-13 | 2020-05-13 | 東レ株式会社 | Core-sheath composite fiber for shrink splitting and woven or knitted fabric containing the same |
-
1998
- 1998-09-30 JP JP27850598A patent/JP3279529B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008088592A (en) * | 2006-09-29 | 2008-04-17 | Kb Seiren Ltd | Core-sheath type conjugated polyester fiber |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2000110029A (en) | 2000-04-18 |
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