JPH03174071A - Low-abrasion and far infrared ray-radiating conjugated fiber - Google Patents
Low-abrasion and far infrared ray-radiating conjugated fiberInfo
- Publication number
- JPH03174071A JPH03174071A JP1308893A JP30889389A JPH03174071A JP H03174071 A JPH03174071 A JP H03174071A JP 1308893 A JP1308893 A JP 1308893A JP 30889389 A JP30889389 A JP 30889389A JP H03174071 A JPH03174071 A JP H03174071A
- Authority
- JP
- Japan
- Prior art keywords
- sheath
- component
- abrasion
- conjugated fiber
- core
- 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.)
- Pending
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 28
- 238000005299 abrasion Methods 0.000 title claims abstract description 7
- 239000000306 component Substances 0.000 claims abstract description 19
- 239000000919 ceramic Substances 0.000 claims abstract description 17
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- 230000005855 radiation Effects 0.000 claims abstract description 10
- 239000008358 core component Substances 0.000 claims abstract description 8
- 229920000728 polyester Polymers 0.000 claims abstract description 7
- 239000002131 composite material Substances 0.000 claims description 17
- -1 polysiloxane Polymers 0.000 abstract description 17
- 229920001296 polysiloxane Polymers 0.000 abstract description 12
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract description 6
- 125000003700 epoxy group Chemical group 0.000 abstract description 2
- 229920002647 polyamide Polymers 0.000 abstract description 2
- 239000000314 lubricant Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 10
- 229910052574 oxide ceramic Inorganic materials 0.000 description 10
- 239000011224 oxide ceramic Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000002216 antistatic agent Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 238000004080 punching Methods 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- LTPBRCUWZOMYOC-UHFFFAOYSA-N Beryllium oxide Chemical compound O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000009960 carding Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 1
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000009830 intercalation Methods 0.000 description 1
- 230000002687 intercalation Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野〉
本発明は遠赤外線を効率よく放射する合成繊維に関する
ものである。さらに詳しくは、摩擦係数が低く、低摩耗
性の遠赤外線放射性複合IINに関する。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a synthetic fiber that efficiently emits far infrared rays.More specifically, it relates to a far infrared emitting composite IIN that has a low coefficient of friction and low abrasion. .
〈従来の技術〉
従来より、アルミナ系、ジルコニア系、マグネシア系或
いはこれらの複合体よりなる酸化物系セラミックスは、
遠赤外線を効率よく放射することが知られている。また
、遠赤外線を用いて物体を加熱する場合、被加熱物体は
直接輻射加熱され、表面と内部との熱伝達時間の差が少
なく、全体がほとんど同時に加熱されること、および有
機高分子化合物に対する加熱効率も高く、人体に対する
暖房感覚もやわらかであることも知られている。<Conventional technology> Conventionally, oxide ceramics made of alumina, zirconia, magnesia, or a composite thereof are
It is known to efficiently radiate far-infrared rays. In addition, when heating an object using far infrared rays, the object to be heated is directly radiant heated, there is little difference in heat transfer time between the surface and the inside, and the entire object is heated almost simultaneously. It is also known that the heating efficiency is high and the heating sensation on the human body is gentle.
近年、上記遠赤外線効果を有する繊維製品をつくるため
に、上記遠赤外線放射能を有する酸化物系セラミックス
を合成繊維に付与する方法が多数提案されている。しか
しながら、セラミックスを含有する処理剤を繊維に付着
せしめる方法は、接着性が乏しく摩擦等による脱落があ
り耐久性に欠ける。また、特開昭63−196710号
公報にて提案されているセラミックスを合成繊維内部に
含有せしめる方法は、十分な遠赤外線効果を得るために
は、セラミックスを含有率を高める必要があるが、その
場合紡糸性が悪くなり、また繊維表面にセラミックスが
露出するため、後加工工程(紡績、力一ド工程等)で繊
維が接触する各種糸導等の装置の摩耗・損傷が著しく工
業生産上問題がある。In recent years, in order to produce textile products having the far-infrared effect, many methods have been proposed for adding oxide ceramics having the far-infrared radiation to synthetic fibers. However, the method of attaching a treatment agent containing ceramics to fibers has poor adhesion and may fall off due to friction, resulting in a lack of durability. Furthermore, the method of incorporating ceramics into synthetic fibers proposed in JP-A No. 63-196710 requires increasing the content of ceramics in order to obtain a sufficient far-infrared effect. In this case, spinnability deteriorates and ceramics are exposed on the fiber surface, causing wear and damage to various yarn guiding devices and other devices that come into contact with the fibers during post-processing processes (spinning, force-pulling processes, etc.), which is a serious problem in industrial production. There is.
かかる後工程での問題を解消するために、セラミックス
を含有するポリマーを芯部に配置する芯鞘型複合繊維が
特開昭63−92720号公報に提案されているが、鞘
部のポリマーが遠赤外線を吸収するために十分な遠赤外
線効果が得られない。また、時開0((63−1269
71M公報には、セラミックスを含有するポリマーを芯
部に配置する芯鞘型複合繊維を使用して!!雑構造物と
した後、該被覆層の少なくとも一部を除去する方法が提
案されているが、製造方法が複雑であり常用には適さな
いといった欠点があった。In order to solve this problem in the post-process, a core-sheath type composite fiber in which a ceramic-containing polymer is disposed in the core has been proposed in JP-A-63-92720; A sufficient far-infrared effect cannot be obtained to absorb infrared rays. Also, time opening 0 ((63-1269
Publication 71M uses a core-sheath type composite fiber in which a polymer containing ceramics is placed in the core! ! A method has been proposed in which at least a portion of the coating layer is removed after forming the structure, but this method has the disadvantage that the manufacturing method is complicated and is not suitable for regular use.
(発明の目的)
本発明は、上記従来技術の有する問題点を背頻になされ
たもので、その目的は、紡糸性が良好であり、取り扱う
際の設備の摩耗・損傷がなく、かつ遠赤外線放射能に優
れた複合muを提供することにある。(Objective of the Invention) The present invention solves the problems of the above-mentioned prior art, and aims to provide good spinnability, no wear or damage to equipment during handling, and far-infrared rays. The object of the present invention is to provide a composite mu with excellent radioactivity.
(発明の構成)
本発明者等は、上記目的−を達成するため鋭意検討した
結果、驚くべきことに、鞘部に遠赤外線放射能を有する
セラミックスを含有する芯鞘複合繊維の表面に特定の処
理剤を付与することによって、遠赤外線放射能を維持し
ながら設備の摩耗を極めて減少させ得ることを見出し本
発明に到達した。(Structure of the Invention) As a result of intensive studies to achieve the above-mentioned object, the present inventors surprisingly found that a specific material is formed on the surface of a core-sheath composite fiber whose sheath portion contains ceramics having far-infrared radiation. The present invention was achieved by discovering that by applying a treatment agent, it is possible to significantly reduce equipment wear while maintaining far-infrared radiation.
すなわち、本発明によれば、遠赤外線放射能を有するセ
ラミックス酸化物を3〜30重量%含有するポリマーを
鞘成分とし、ポリエステルを芯成分とする芯鞘型複合1
!維であって、該複合繊維の表面にはシリコン成分を主
体とする平滑性処理剤が有効成分として4111重量に
対して0.2〜5重量%付着していることを特徴とする
低摩耗性遠赤外線放射性複合繊維が提供される。That is, according to the present invention, a core-sheath type composite 1 having a polymer containing 3 to 30% by weight of a ceramic oxide having far-infrared radiation as a sheath component and a polyester as a core component
! A low abrasion fiber, characterized in that a smoothing agent mainly composed of silicone is attached to the surface of the composite fiber in an amount of 0.2 to 5% by weight based on the weight of 4111 as an active ingredient. A far-infrared emissive composite fiber is provided.
本発明において使用される酸化物セラくツクスとしては
、例えば、アルミナ(Auz Oa )系。The oxide ceramics used in the present invention include, for example, alumina (AuzOa)-based ceramics.
マグネシア(IvloO)系、ジルコニア(Zr 02
)系、チタニア(T! 02 )系の外、二酸化ケイ
素(SfOz)、酸化クロム(Cr 202 )、 7
エライト(「eOz ・Fe a 04 ) 、 スピ
ネル(MgO−A1203〉、セリア(Ce 02 )
。Magnesia (IvloO) series, zirconia (Zr 02
) series, titania (T! 02 ) series, silicon dioxide (SfOz), chromium oxide (Cr 202 ), 7
Elite ("eOz ・Fe a 04), Spinel (MgO-A1203>, Ceria (Ce 02)
.
ベリリア(Be O)等があげられる。かかるセラミッ
クスのうち、30℃における遠赤外線放射率が4.5〜
30μ卯の領域で65%以上を有することが好ましく、
特に75%以上が望ましい。また、酸化物セラミックス
は微粉砕して粒径5μ卯以下、好ましくは1μ班以下に
して使用するのが望ましい。Examples include beryllia (Be O). Among such ceramics, far infrared emissivity at 30°C is 4.5 to
It is preferable to have 65% or more in an area of 30 μm,
In particular, 75% or more is desirable. Further, it is desirable to use the oxide ceramics by finely pulverizing the particles to a particle size of 5 μm or less, preferably 1 μm or less.
酸化物セラミックスを繊維形成性ポリマー中に含有せし
める方法としては、該ポリマーの重合工程で加える方法
、マスターチップとして紡糸工程にてペースチップと混
練する方法等いずれの方法を採用してもよいが、酸化物
セラミックスの分散状態が均一となって紡糸性が向上す
る点から、2軸ルーダ−を用いマスターチップとペース
チップとを混合溶融紡糸するのが好ましい。As a method for incorporating oxide ceramics into the fiber-forming polymer, any method may be adopted, such as adding it in the polymerization process of the polymer, or kneading it as a master chip with a pace chip in the spinning process. It is preferable to mix and melt-spun the master chip and the pace chip using a twin-screw router, since the dispersion state of the oxide ceramic becomes uniform and the spinning properties are improved.
本発明の複合I維製造に用いられる鞘成分用のポリマー
は特に限定する必要はないが、熱可塑性ポリマー、例え
ばポリエチレン、ポリプロピレン等のポリオレフィン、
ポリエチレンテレフタレート、ポリブチレンテレフタレ
ート等のポリエステル、ナイロン−6、ナイロン−6,
6等のポリアミド等が好ましく用いられる。The polymer for the sheath component used in the production of the composite I fiber of the present invention does not need to be particularly limited, but includes thermoplastic polymers, such as polyolefins such as polyethylene and polypropylene,
Polyesters such as polyethylene terephthalate and polybutylene terephthalate, nylon-6, nylon-6,
Polyamide such as No. 6 is preferably used.
一方、芯成分用のポリマーとしては、Il維形成能が優
れている必要があるので、例えばポリエチレンテレフタ
ート、ポリブチレンテレフタレート等のポリエステルが
用いられる。すなわち本発明においては、鞘成分として
セラくツクス酸化物を含有するポリマーを使用するため
、鞘成分のみでは曳糸性が悪くかつIll動物性劣った
ものしか得られないので、芯成分により紡糸性を良好に
すると共に!III物性を優れたものとする必要がある
のである。On the other hand, as the polymer for the core component, polyesters such as polyethylene terephthalate and polybutylene terephthalate are used, since it is necessary to have excellent Il fiber-forming ability. In other words, in the present invention, since a polymer containing serrax oxide is used as a sheath component, the sheath component alone provides poor spinnability and poor quality. Along with making it better! III. It is necessary to have excellent physical properties.
鞘成分中のセラミックス酸化物の含有量は3〜30重量
%、好ましくは5〜15重量%とする必要がある。含有
量が3重量%未満では遠赤外線放射性能が不十分で満足
すべき性能は得られない。一方30重量%を超えると、
複合繊維の紡糸性が低下して繊維化が困難になるだけで
なく、繊維物性も劣ったものとなるため好ましくない。The content of ceramic oxide in the sheath component should be 3 to 30% by weight, preferably 5 to 15% by weight. If the content is less than 3% by weight, far-infrared radiation performance is insufficient and satisfactory performance cannot be obtained. On the other hand, if it exceeds 30% by weight,
This is undesirable because not only the spinnability of the composite fiber decreases and fiberization becomes difficult, but also the physical properties of the fiber deteriorate.
鞘成分と芯成分の比率(重量)は70/ 30〜40/
60の範囲であることが好ましい。芯成分の比率が少な
くなると、紡糸性が悪くなり、−5鞘成分の比率が少な
くなると、十分な遠赤外線放射性能を得るためには、鞘
成分中のセラミックス酸化物の含有量を多くする必要が
あり、紡糸性が悪くなる。The ratio (weight) of sheath component and core component is 70/30-40/
A range of 60 is preferred. When the ratio of the core component decreases, spinnability deteriorates, and when the ratio of the -5 sheath component decreases, it is necessary to increase the content of ceramic oxide in the sheath component in order to obtain sufficient far-infrared radiation performance. This results in poor spinnability.
本発明においては、以上に述べた酸化物セラミックスを
含有する複合繊維の表面に、シリコン成分を主体とする
平滑性処理剤を0.2〜5重量%(m維重量に対して)
付与することが肝要である。In the present invention, 0.2 to 5% by weight (based on the weight of m fibers) of a smoothing agent mainly containing a silicon component is applied to the surface of the composite fiber containing the above-mentioned oxide ceramics.
It is important to provide this.
なおここでいう「主体とする」とは、処理剤中のシリコ
ン成分の含有量が60重量%以上であることを言い、シ
リコン成分の含有量がこれ未満にあっては、得られる繊
維のIliwAを低下せしめる効果が小さくなる傾向が
ある。Note that "containing mainly" here means that the content of the silicon component in the treatment agent is 60% by weight or more, and if the content of the silicon component is less than this, the IliwA of the obtained fibers will be reduced. There is a tendency for the effect of reducing the
シリコン成分としては、ジメチルポリシロキサン、ジフ
ェニルポリシロキサン等非反応性ポリシロキサンを単独
で使用しても良いが、m粒表面で反応硬化した皮膜を形
成する成分、例えば、メチルハイドロジエンポリシロキ
サン、エポキシ基含有ポリシロキサン、アミノ基含有ポ
リシロキサン。As the silicone component, non-reactive polysiloxanes such as dimethylpolysiloxane and diphenylpolysiloxane may be used alone, but components that form a reaction-cured film on the m-grain surface, such as methylhydrodienepolysiloxane, epoxy Group-containing polysiloxane, amino group-containing polysiloxane.
オキシアルキレン基含有ポリシロキサン、メチルごニル
ポリシロキサン、アルコキシポリシロキサン等の反応性
ポリシロキサンを、単独もしくは混合して用いる、ある
いは前記非反応性ポリシロキサンと混合して用いること
は、処理剤自体の機械的特性が向上して摩擦を低下せし
める効果の耐久性が向上するとともに、遠赤外線放射能
を低減せしめることがないため特に好ましい。さらには
、アミノシラン等の低分子架橋剤を添加して架橋性を改
善せしめた処理剤であってもよい。なお、シリコン成分
は一般に帯電防止性が小さいので、少量の帯電防止剤を
併用するのが好ましい。カチオン系、アニオン系いずれ
の系統の帯電防止剤でもよいが、通常用いられているも
のをそのまま利用すればよい。The use of reactive polysiloxanes such as oxyalkylene group-containing polysiloxanes, methylpolysiloxanes, and alkoxypolysiloxanes alone or in combination with the above-mentioned non-reactive polysiloxanes may result in It is particularly preferable because the mechanical properties are improved and the durability of the effect of reducing friction is improved, and far-infrared radiation is not reduced. Furthermore, it may be a processing agent whose crosslinking properties are improved by adding a low-molecular crosslinking agent such as aminosilane. In addition, since silicon components generally have low antistatic properties, it is preferable to use a small amount of antistatic agent in combination. Any type of antistatic agent, cationic or anionic, may be used, and commonly used antistatic agents may be used as they are.
かかる処理剤をmr4に付与するには、溶液状態。In order to apply such a treatment agent to mr4, it is in a solution state.
エマルジョン状態、いずれの状態で付与してもよいが、
その付着量を有効成分として0.2〜5重量%(繊維重
量に対して〉、好ましくは0.5〜3重置%とする必要
がある。0.2重量%未満の場合には、平滑性が不十分
となって酸化物セラミックスによる設備の摩耗を解消す
ることはできなくなる。It can be applied in either emulsion state or
It is necessary to adjust the amount of the active ingredient to 0.2 to 5% by weight (relative to the weight of the fiber), preferably 0.5 to 3% by weight. As a result, the wear of equipment caused by oxide ceramics cannot be eliminated.
一方、5重量%を越えると平滑性が高くなりすぎて、カ
ード工程等でのlllI間格合性が低下し均一なウェブ
及び紡績糸が得られなくなる。On the other hand, if it exceeds 5% by weight, the smoothness becomes too high, the IllI intercalation property in the carding process etc. deteriorates, and a uniform web and spun yarn cannot be obtained.
なお、処理剤をエマルジョンとして使用する場合には、
通常用いられる乳化剤を併用するのがよい。In addition, when using the processing agent as an emulsion,
It is preferable to use commonly used emulsifiers.
(発明の効果)
本発明の遠赤外線放射性複合IIIは、表面にポリシロ
キサン処理剤が付与せしめられているので、従来多発し
ていた設備の摩耗・損傷がなく、かつ良好な遠赤外線放
射能を有する品質に優れた紡績系、不織布等を効率よく
生産することが可能となる。(Effects of the Invention) The far-infrared emissive composite III of the present invention has a polysiloxane treatment agent applied to its surface, so there is no wear and tear on equipment, which has occurred frequently in the past, and it has good far-infrared radiation. It becomes possible to efficiently produce spinning systems, nonwoven fabrics, etc. with excellent quality.
(実施例) 以下、実施例により本発明をさらに具体的に説明する。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例1〜4.比較例1〜3
波長4.5〜30μ風の範囲内の放射率が、30℃にお
いて70%以上で平均放射率が75%、平均粒径0.9
μ卯のセラミックス酸化物(zrOz/S!Oz /
Fe 203−64/35/ 1)と、230℃におけ
るメルトインデックス50のポリプロピレン微粉末とを
混合した後、溶融してセラミックス酸化物を40重量%
含有したマスターチップを作成した。Examples 1-4. Comparative Examples 1 to 3 The emissivity within the wavelength range of 4.5 to 30μ wind is 70% or more at 30°C, the average emissivity is 75%, and the average particle size is 0.9
μU ceramic oxide (zrOz/S!Oz/
Fe 203-64/35/1) and polypropylene fine powder with a melt index of 50 at 230°C are mixed and then melted to form a ceramic oxide of 40% by weight.
A master chip containing the following was created.
次いでこのマスターチップと230℃におけるメルトイ
ンデックス50のポリプロピレンを1:3の割合でチッ
プブレンドし、2軸ルーダ−を用いて、230℃で溶融
し鞘成分とし、極限粘度0.64のポリエチレンテレフ
タレートを芯成分とし吐出重量比50:50になるよう
に芯鞘型複合紡糸装置に供給し、孔径0.5Mφの口金
より紡出して紡速700m/ winで捲取った。Next, this master chip and polypropylene with a melt index of 50 at 230°C were blended at a ratio of 1:3, and melted at 230°C using a twin-screw router to form a sheath component, and polyethylene terephthalate with an intrinsic viscosity of 0.64 was mixed. The core component was supplied to a core/sheath type composite spinning device at a discharge weight ratio of 50:50, spun through a nozzle with a hole diameter of 0.5 Mφ, and wound up at a spinning speed of 700 m/win.
得られた未延伸糸を集束して400万デニールとし、温
水中70℃で3倍に延伸し、表1記載の処理剤を種々の
有効成分付着量となるよう付与し、次いで捲縮を付与し
た後140℃で熱処理して繊維長51、にカットした。The obtained undrawn yarn was bundled to 4 million denier, stretched 3 times in hot water at 70°C, treated with the treatment agents listed in Table 1 to give various amounts of active ingredients, and then crimped. After that, it was heat-treated at 140°C and cut into fibers with a length of 51.
得られた繊維は単繊度6デニールで酸化物セラミックス
の複合II雑鞘層内の分散は均一であった( 3000
倍の電子顕微鏡でIl察)。The obtained fibers had a single denier of 6 denier and were uniformly dispersed in the composite II miscellaneous sheath layer of oxide ceramics (3000
(Illustrated under a magnified electron microscope).
得られた繊維をローラーカードに通して100g/TI
tのウェブを作成した後、繊維間交絡性向上のためフエ
ラー社製ニードルパンチ機にてバーブ#36レギユラー
パンチ密度30F/cd両面打ち、n入深19m+の条
件にてニードルリングした。The obtained fiber was passed through a roller card at 100g/TI.
After creating a web of T, needle punching was performed using a needle punch machine manufactured by Feller under the conditions of barb #36 regular punch density 30F/cd double-sided punching and n depth of 19m+ in order to improve the entanglement between fibers.
カード工程及びニードルパンチ工程での設備の摩耗、針
落ち等の結果を表−1に示す。Table 1 shows the results of equipment wear, needle drops, etc. in the carding process and needle punching process.
また、得られた不織布を腕に付着させ、皮膚温の変化を
測定した。結果を表−1にあわせて示す。In addition, the obtained nonwoven fabric was attached to the arm, and changes in skin temperature were measured. The results are also shown in Table-1.
実施例5〜8.比較例4〜5
酸化物セラミックスの種類及び配合量を表2に記載の如
く変更した外は全て実施例1と同様にして不織布を得た
。この結果を表−2に示す。Examples 5-8. Comparative Examples 4 to 5 Nonwoven fabrics were obtained in the same manner as in Example 1, except that the type and amount of oxide ceramics were changed as shown in Table 2. The results are shown in Table-2.
Claims (1)
0重量%含有するポリマーを鞘成分とし、ポリエステル
を芯成分とする芯鞘型複合繊維であって、該複合繊維の
表面にはシリコン成分を主体とする平滑性処理剤が有効
成分として、繊維重量に対して0.2〜5重量%付着し
ていることを特徴とする低摩耗性遠赤外線放射性複合繊
維。3 to 3 ceramic oxides with far-infrared radiation
It is a core-sheath type composite fiber having a polymer containing 0% by weight as a sheath component and a polyester as a core component. A low abrasion far-infrared emissive composite fiber characterized in that it has an adhesion of 0.2 to 5% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1308893A JPH03174071A (en) | 1989-11-30 | 1989-11-30 | Low-abrasion and far infrared ray-radiating conjugated fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1308893A JPH03174071A (en) | 1989-11-30 | 1989-11-30 | Low-abrasion and far infrared ray-radiating conjugated fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03174071A true JPH03174071A (en) | 1991-07-29 |
Family
ID=17986534
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1308893A Pending JPH03174071A (en) | 1989-11-30 | 1989-11-30 | Low-abrasion and far infrared ray-radiating conjugated fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03174071A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014189937A (en) * | 2013-03-28 | 2014-10-06 | Unitika Trading Co Ltd | Functional fiber |
JP2017125293A (en) * | 2017-03-06 | 2017-07-20 | ユニチカトレーディング株式会社 | Functional fiber |
-
1989
- 1989-11-30 JP JP1308893A patent/JPH03174071A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014189937A (en) * | 2013-03-28 | 2014-10-06 | Unitika Trading Co Ltd | Functional fiber |
JP2017125293A (en) * | 2017-03-06 | 2017-07-20 | ユニチカトレーディング株式会社 | Functional fiber |
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