JPH02160921A - Far infrared ray emitting polyester staple fiber - Google Patents
Far infrared ray emitting polyester staple fiberInfo
- Publication number
- JPH02160921A JPH02160921A JP63314325A JP31432588A JPH02160921A JP H02160921 A JPH02160921 A JP H02160921A JP 63314325 A JP63314325 A JP 63314325A JP 31432588 A JP31432588 A JP 31432588A JP H02160921 A JPH02160921 A JP H02160921A
- Authority
- JP
- Japan
- Prior art keywords
- ceramic particles
- infrared ray
- far infrared
- fiber
- ray emitting
- 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 35
- 229920000728 polyester Polymers 0.000 title claims abstract description 25
- 239000002245 particle Substances 0.000 claims abstract description 28
- 229920000642 polymer Polymers 0.000 claims abstract description 26
- 239000000919 ceramic Substances 0.000 claims abstract description 23
- -1 polyethylene terephthalate Polymers 0.000 abstract description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 7
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000395 magnesium oxide Substances 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 9
- 239000002131 composite material Substances 0.000 description 8
- 238000009987 spinning Methods 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000009960 carding Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000191 radiation effect Effects 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- HIJLKWFRGYZKKL-UHFFFAOYSA-N [O-2].[Ti+4].[Au+3] Chemical compound [O-2].[Ti+4].[Au+3] HIJLKWFRGYZKKL-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- SXQXMCWCWVCFPC-UHFFFAOYSA-N aluminum;potassium;dioxido(oxo)silane Chemical compound [Al+3].[K+].[O-][Si]([O-])=O.[O-][Si]([O-])=O SXQXMCWCWVCFPC-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Nonwoven Fabrics (AREA)
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、遠赤外線放射性を有する中空断面形状のポリ
エステルステープμ繊維に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a polyester staple μ fiber having a hollow cross-sectional shape and having far-infrared radiation.
遠赤外線の繊維素材への利用法については数多(提案さ
れ、その一つは後加工によるものであり、特開昭60−
239543号公報には繊維の表面に遠赤外線放射性セ
ラミック粉末をコーティングすることが示されておシ、
また実開昭62−197552号公報には布に遠赤外線
放射性のセラミックス粉末を塗布することが示されてい
るが、これらの方法では加工コストがかさみ、繊維表面
のセラミックスが脱落し易い等の欠点を有していた。Many methods have been proposed for using far infrared rays on textile materials, one of which is post-processing;
Publication No. 239543 discloses coating the surface of fibers with far-infrared emissive ceramic powder.
Furthermore, Japanese Utility Model Application No. 62-197552 discloses applying far-infrared emissive ceramic powder to cloth, but these methods have drawbacks such as high processing costs and the tendency for ceramics on the fiber surface to fall off. It had
また他の一つは複合紡糸によるものであり、特開昭62
−238823号公報には芯鞘複合繊維の芯部の素材に
セラミック粉末、鞘部の素材にナイロン等のポリマーを
用いること、また特開昭63−92720号公報には芯
鞘複合繊維の芯部に遠赤外線放射性の粒子を含むポリマ
ーを配置することがそれぞれ示されているが、いずれも
練シ込みタイプであるので粒子の脱落がなく、効果が半
永久的であり耐洗濯性にも優れている。しかしステープ
μとしての用途はインテリアの寝装分野が主体であり、
こたつ布団の例を挙げるまでもな(、嵩高性がとりわけ
重視されるが、芯鞘複合繊維では嵩高性を発揮出来ない
という致命的な欠点があった。The other method is based on composite spinning, which was disclosed in Japanese Patent Application Laid-open No. 62
JP-A-238823 discloses that ceramic powder is used as the material for the core of the core-sheath composite fiber, and a polymer such as nylon is used as the material for the sheath. It has been shown that polymers containing particles that emit far-infrared rays are placed in each type, but since they are all kneaded type, the particles do not fall off, the effect is semi-permanent, and they have excellent washing resistance. . However, the main use of Staple μ is in the interior bedding field.
There is no need to take the example of a kotatsu futon (bulkness is particularly important, but core-sheath composite fibers have a fatal drawback of not being able to exhibit bulkiness).
本発明は上記の如き従来の問題点を解消し、セラミック
粒子の脱落がなく、また嵩高性を奏しうる遠赤外線放射
性を有するポリエステルステープル繊維を提供するもの
である。The present invention solves the above-mentioned conventional problems and provides a polyester staple fiber that does not cause shedding of ceramic particles and has far-infrared radiation and is bulky.
本発明はアルミナ、マグネシア及びジルコニアの群から
選ばれる少なくとも1種の遠赤外線放射性を有するセラ
ミック粒子を1〜15wt%含有するポリエステルポリ
マーからなυ中空断面形状を有する遠赤外線放射性ポリ
エステルステープル繊維にある。The present invention is directed to a far-infrared emitting polyester staple fiber having a hollow cross-sectional shape and made of a polyester polymer containing 1 to 15 wt % of at least one far-infrared emitting ceramic particle selected from the group of alumina, magnesia, and zirconia.
本発明において使用する遠赤外線放射性セラミック粒子
としては例えばセリサイトが好ましく挙げられる。セリ
サイトは塩基性ケイ酸アルミニウム・カリウム(K、0
−3A40s−ilo、−2H,0)で白色粉末状であ
って、その粒径は0.1〜1.5μmが好ましい。粒径
が0,1μm未満であると粒子の凝集が発生し易くなシ
、紡糸時にフィルター目詰シが発生し紡糸不調となる。As the far-infrared emitting ceramic particles used in the present invention, for example, sericite is preferably mentioned. Sericite is basic potassium aluminum silicate (K, 0
-3A40s-ilo, -2H,0) and is in the form of a white powder, and its particle size is preferably 0.1 to 1.5 μm. If the particle size is less than 0.1 μm, particle aggregation is not likely to occur, and filter clogging occurs during spinning, resulting in poor spinning performance.
逆に粒径が1.5μmを超えると粒径の大きさ自体が障
害となり紡糸時にフィルター目詰りを惹起し、圧力上昇
等の問題を誘発する。On the other hand, if the particle size exceeds 1.5 μm, the particle size itself becomes an obstacle, causing filter clogging during spinning and causing problems such as pressure increase.
次ニセラミック粒子のポリエステルポリマー中の含有率
については1〜15 wt%が好ましい。The content of secondary ceramic particles in the polyester polymer is preferably 1 to 15 wt%.
含有率が1 wtチ未満であると繊維製造上は特に問題
ないが、遠赤外線放射効果が小さくなり、特徴とする機
能を発揮し得ない。If the content is less than 1 wt, there is no particular problem in fiber production, but the far-infrared radiation effect becomes small and the characteristic functions cannot be exhibited.
逆に含有率が15 wt%を超えると、遠赤外線放射効
果は大きくなることが期待されるが、紡糸時の曳糸性が
不良となり安定して紡糸することが不可能となる。On the other hand, if the content exceeds 15 wt%, the far-infrared radiation effect is expected to increase, but the spinnability during spinning becomes poor and stable spinning becomes impossible.
本発明におけるポリエステルポリマーとしては通常の繊
維形成性ポリエステルのことで、特に限定されないが、
例えばテレフタル酸或いはそのエステルを主たるジカル
ボン酸成分とし、グリコール成分としてエチVングリコ
ーμを主たるグリコール成分とするポリエチレンテレフ
タレートが好ましい。The polyester polymer used in the present invention refers to ordinary fiber-forming polyesters, and is not particularly limited.
For example, polyethylene terephthalate containing terephthalic acid or its ester as the main dicarboxylic acid component and ethyl V glycol μ as the main glycol component is preferred.
このジカルボン酸成分の一部を、例えばアジピン酸、セ
パシン酸等のジカルボン酸またはそのエステル、p−オ
キシ安息香酸、p−β−オキシエトキシ安息香酸等のオ
キシカμボン酸またはそのエステルで置き換えてもよく
、またグリコ−μ成分の一部を例えばテトヲメチVング
リコール、1,4−ビス(β−オキシエトキシ)ベンゼ
ン、ビスフェノ−/L’Aのビスグリコールエーテル、
ポリアルキレングリコール等のグリコ−μで置き換える
こともできる。A part of this dicarboxylic acid component may be replaced with a dicarboxylic acid such as adipic acid or sepacic acid or an ester thereof, or an oxycarboxylic acid such as p-oxybenzoic acid or p-β-oxyethoxybenzoic acid or an ester thereof. Often, a part of the glyco-μ component may be substituted with, for example, tetramethylene glycol, 1,4-bis(β-oxyethoxy)benzene, bisphenol/L'A bisglycol ether,
Glyco-μ such as polyalkylene glycol can also be substituted.
本発明における遠赤外線放射性を有するセラミック粒子
のポリエステルポリマーへの練込み方法としてはセラミ
ック粒子をポリエステルポリマーの重合工程で添加する
方法、マスターバッチ化したのちポリエステルポリマー
と混錬する方法、粒子を予めポリエステルポリマーと溶
融スるかポリエステルポリマーと相溶性のある分散剤、
可塑剤等と混合してスラリー状とした組成物を押出機前
のポリエステル繊維ツFに加えるか又は紡糸直前の溶融
ポリマーに加えて混錬分散を行なう方法等がある。In the present invention, methods for kneading ceramic particles with far-infrared radiation into a polyester polymer include adding the ceramic particles during the polymerization process of the polyester polymer, forming a masterbatch and then kneading it with the polyester polymer, and adding the ceramic particles to the polyester polymer in advance. a dispersant that is compatible with the polyester polymer that melts with the polymer;
There are methods of kneading and dispersing the composition by mixing it with a plasticizer and the like and adding it to the polyester fiber F before the extruder, or adding it to the molten polymer just before spinning.
ポリエステルステープル繊維は保温性に優れた特徴を発
揮するため、こたつ布団等の用途にとシわけ有用であっ
て、更に他の特性として嵩高性の要求もあることから、
繊維の断面形状は中空断面形状であるのが好ましい。Polyester staple fibers exhibit excellent heat retention properties, making them particularly useful for applications such as kotatsu futons, and they are also required to have bulk as another characteristic.
Preferably, the cross-sectional shape of the fiber is a hollow cross-sectional shape.
第1図(イ)、(ロ)に本発明のステーブル繊維の例の
断面図でAはセラミック粒子含有ポリマーBは中空部、
Cはセラミック粒子を含有しないポリマーを示す。Figures 1 (a) and (b) are cross-sectional views of examples of stable fibers of the present invention, where A is a ceramic particle-containing polymer B is a hollow part,
C indicates a polymer containing no ceramic particles.
また、第2図(イ)、(ロ)、(ハ)は本発明の第1図
に)の中空複合ポリエステルステープル繊維を製造する
ために用いられる複合紡糸口金装置の例の縦断面図であ
る。ここで第2図(イ)の3は分配板、4は前板、5は
ノズル板を示す。更に第2図(ロ)は前板吐出孔のX
−X’断面図、第2図(ハ)はノズル板吐出孔のy−y
’断面図である。ポリエステル繊維には任意の手段で捲
縮を付与でき、例えば繊維の中空複合化による捲縮、機
械的外手段による捲縮等により任意の巻縮を付与手段を
適用しうる。FIGS. 2(a), 2(b), and 2(c) are longitudinal cross-sectional views of an example of a composite spinneret device used for producing the hollow composite polyester staple fiber shown in FIG. 1 of the present invention. . Here, 3 in FIG. 2(A) indicates a distribution plate, 4 indicates a front plate, and 5 indicates a nozzle plate. Furthermore, Fig. 2 (b) shows the X of the front plate discharge hole.
-X' sectional view, Figure 2 (c) is y-y of the nozzle plate discharge hole
'This is a cross-sectional view. The polyester fibers can be crimped by any means, such as crimping by forming hollow fibers into composite fibers, crimping by external mechanical means, or the like.
また本発明のポリエステル繊維のステーブルとしての繊
維長は32〜128mが適当である。Further, the suitable fiber length of the polyester fiber of the present invention as a stable fiber is 32 to 128 m.
繊維長が32−未満ではカーデイングにおける繊維の絡
みが小さくなシ綿切れの問題が発生し易くなり、逆に1
28wmを超えるとカーデイング時のプロセス性が悪く
なる。If the fiber length is less than 32mm, the problem of fiber tangles being small during carding and cotton breakage is likely to occur;
If it exceeds 28wm, processability during carding will deteriorate.
本発明のポリエステル繊維にはセラミック粒子の他、酸
化防止剤、安定剤、分散助剤、抗菌剤、消臭剤、難燃剤
、着色剤、紫外線吸収剤等の改質剤や機能付与剤が含有
されていてもよい。In addition to ceramic particles, the polyester fiber of the present invention contains modifiers and functional agents such as antioxidants, stabilizers, dispersion aids, antibacterial agents, deodorants, flame retardants, colorants, and ultraviolet absorbers. may have been done.
以下、実施例を用いて本発明を更に詳細に説明する。 Hereinafter, the present invention will be explained in more detail using Examples.
実施例中の中空率(2))は次式によって算出した。The hollow ratio (2) in Examples was calculated by the following formula.
嵩高性は、原綿をカードで開繊して得たウェブ80t(
サイズ20倒×20譚)に荷重(サイズ20αX20副
、重さ170F)をかけた時の比容積(QC/f)とし
て求めた。The bulkiness was determined by a web of 80t (80t) obtained by opening raw cotton with a card.
It was calculated as a proportion volume (QC / F) when the load (size 20αx20 vendor, weight 170F) was applied to the size 20 defeat x 20 tan).
実施例1
セリサイト系セラミック(斐川砿業製斐川マイカz−2
0、平均粒径0.2μm)を15 wt%含むポリエチ
レンテレフタレートポリマー(相対粘度t 63.25
℃メタクレゾール中で測定)のマスターバッチと酸化チ
タンをCL 5 wt%含むポリエチレンテレフタV−
)ポリマー(相対粘度1.6 り )とを重量比でi:
2.75に均一にブレンドして、ポリマーに対しセラミ
ック粒子を4 wt%含むチップを片側成分とし、他方
成分として酸化チタンを[L 50 wt%含むポリエ
チレンテレフタレートポリマー(相対粘度1.63 )
のチップをそれぞれ別個の押出機に供給し、第1表に示
す温度で溶融したあと、ギヤポンプで比率1:1で第2
図に示す複合紡糸口金装置に導き283℃で複合紡糸し
た。前板は吐出孔を直径0.5 wm 、前板とノズル
板との間隔を0,2瓢とした。ノズル板の吐出孔は第2
図(ハ)に示す形状(W=α3+alI、 t=0.1
5w、R: 1. a m )のものを用いた。Example 1 Sericite ceramic (Hikawa Mica Z-2 manufactured by Hikawa Togyo Co., Ltd.)
Polyethylene terephthalate polymer (relative viscosity t 63.25) containing 15 wt% of
Polyethylene terephtha V- containing a masterbatch of 5 wt % of titanium oxide (measured in metacresol) and titanium oxide.
) polymer (relative viscosity 1.6) and weight ratio i:
A polyethylene terephthalate polymer (relative viscosity 1.63) containing titanium oxide [L 50 wt%] was homogeneously blended with 2.75 and a chip containing 4 wt% ceramic particles based on the polymer as one component, and titanium oxide as the other component.
After feeding the chips into separate extruders and melting them at the temperatures shown in Table 1, a second
The mixture was introduced into the composite spinneret device shown in the figure and composite spun at 283°C. The discharge hole of the front plate had a diameter of 0.5 wm, and the distance between the front plate and the nozzle plate was 0.2 mm. The discharge hole of the nozzle plate is the second
The shape shown in figure (c) (W=α3+alI, t=0.1
5w, R: 1. am) was used.
紡出した糸条は、常法に従って空冷し油剤を付与したあ
と680m/分で引き取り集束した。The spun yarn was air-cooled and coated with an oil agent according to a conventional method, and then taken up and bundled at 680 m/min.
この未延伸糸を25℃、65%R,Lの条件下で20時
間シーズニングし、延伸機にて90m/分で4倍に延伸
し、押込捲縮装置にて捲縮を賦与した後、長さ64+w
aに切断し、150℃でヒートセラFした。This undrawn yarn was seasoned for 20 hours at 25°C and 65% R and L, stretched four times at 90 m/min using a drawing machine, and crimped using a push-crimping device. Sa64+w
It was cut into pieces a and subjected to heat cera F at 150°C.
この様にして得られた繊維の糸質、不織布ウェブの嵩高
性等を第1表に示した。Table 1 shows the yarn quality of the fibers thus obtained, the bulkiness of the nonwoven web, etc.
実施例2
押出機の溶融温度を共通の285℃に設定した以外は実
施例1と同様に行った。Example 2 The same procedure as in Example 1 was carried out except that the melting temperature of the extruder was set at a common 285°C.
この様にして得られた繊維の糸質、不織布ウェブの嵩高
性等を第1表に示した。Table 1 shows the yarn quality of the fibers thus obtained, the bulkiness of the nonwoven web, etc.
実施例3
セリサイト系セラミック(斐川砿業製斐川マイカz−2
0、平均粒径α2μm)を15wtチ含むポリエチレン
テレフタレートポリマー(相対粘度t 63 )のマス
ターパッチと酸化チタン金o、 s wtチ含むポリエ
チレンテレフタレートポリマー(相対粘度1.63 )
とを重量比で1=6.5に均一にブレンドして、ポリマ
ーに対しセラミック粒子を2 vt%含むチップとし、
これを押出機に供給して第1表に示す温度で溶融した以
外は実施例1と同様に行い、得られた繊維の糸質、不織
布ウェブの嵩高性等を第1表に示した。Example 3 Sericite-based ceramic (Hikawa Mica Z-2 manufactured by Hikawa Togyo Co., Ltd.
A master patch of polyethylene terephthalate polymer (relative viscosity t 63 ) containing 15 wt of titanium oxide (0, average particle size α2 μm) and a polyethylene terephthalate polymer (relative viscosity 1.63) containing titanium oxide gold (o, s wt).
and are uniformly blended at a weight ratio of 1=6.5 to make a chip containing 2 vt% of ceramic particles to the polymer,
The same procedure as in Example 1 was carried out except that this was fed to an extruder and melted at the temperature shown in Table 1, and Table 1 shows the yarn quality of the obtained fibers, the bulkiness of the nonwoven web, etc.
実施例4
押出機の溶融温度を共通の285℃に設定した以外は、
実施例3と同様に行い、得られた繊維の糸質、不織布ウ
ェブの嵩高性等を第1表に示した。Example 4 Except that the melt temperature of the extruder was set at a common 285°C,
It was carried out in the same manner as in Example 3, and the yarn quality of the obtained fibers, the bulkiness of the nonwoven web, etc. are shown in Table 1.
比較例1
繊維の断面を通常の円形断面とした以外は、実施例2と
同様に行い、得られた繊維の糸質、不織布ウェブの嵩高
性等を第1表に示した。Comparative Example 1 The same procedure as in Example 2 was carried out except that the cross section of the fiber was changed to a normal circular cross section, and the yarn quality of the obtained fiber, the bulkiness of the nonwoven web, etc. are shown in Table 1.
比較例2
酸化チタンQ、 5 vt%のみを含むポリエチレンテ
レフタレートポリマー(相対粘度t 63 )チップを
別個の押出機に供給して第1表に示す温度で溶融した以
外は実施例1と同様に行い、得られた繊維の糸質、不織
布ウェブの嵩高性等を第1表に示した。Comparative Example 2 Same as Example 1 except that polyethylene terephthalate polymer (relative viscosity t 63 ) chips containing only 5 vt% titanium oxide Q were fed into a separate extruder and melted at the temperatures shown in Table 1. Table 1 shows the yarn quality of the obtained fibers, the bulkiness of the nonwoven web, etc.
比較例3
押出機の溶融温度を共通の285℃に設定した以外は比
較例1と同様に行い、得られた繊維の糸質、不織布ウェ
ブの嵩高性等を第1表に示した。Comparative Example 3 The same procedure as Comparative Example 1 was carried out except that the melting temperature of the extruder was set at a common 285° C., and the yarn quality of the obtained fibers, the bulkiness of the nonwoven web, etc. are shown in Table 1.
本発明の遠赤外線放射性ポリエステルステープル繊維は
耐久性のある遠赤外放射特性を有し、且つ嵩高性に特に
優れているので、こたつ布団等のインテリア寝装分野に
好適に使用される。The far-infrared emitting polyester staple fiber of the present invention has durable far-infrared radiation characteristics and is particularly excellent in bulk, so it is suitably used in the field of interior bedding such as kotatsu futons.
第1図(梢、(ロ)は本発明の繊維の例の横断面図、第
2図(イ)、(ロ)、(ハ)は本発明の繊維を製造する
紡糸口金装置の例の縦断面図及びその部分断面図である
。
A・・・セラミック粒子含有ポリマー
r・・・中空部
代理人 弁理士 吉 沢 敏 夫
氷1
国
(イ2
r′0)
(四)
(ハンFigure 1 (treetops), (b) is a cross-sectional view of an example of the fiber of the present invention, and Figures 2 (a), (b), and (c) are longitudinal cross-sections of an example of a spinneret device for producing the fiber of the present invention. They are a top view and a partial cross-sectional view thereof.
Claims (1)
少なくとも1種の遠赤外線放射性を有する平均粒径0.
1〜1.5μmのセラミツク粒子を1〜15wt%含有
するポリエステルポリマーからなり中空断面形状を有す
る遠赤外線放射性ポリエステルステープル繊維。An average particle diameter of 0.000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 time days
A far-infrared emitting polyester staple fiber having a hollow cross-sectional shape and made of a polyester polymer containing 1 to 15 wt% of ceramic particles of 1 to 1.5 μm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63314325A JPH02160921A (en) | 1988-12-13 | 1988-12-13 | Far infrared ray emitting polyester staple fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63314325A JPH02160921A (en) | 1988-12-13 | 1988-12-13 | Far infrared ray emitting polyester staple fiber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02160921A true JPH02160921A (en) | 1990-06-20 |
Family
ID=18051978
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63314325A Pending JPH02160921A (en) | 1988-12-13 | 1988-12-13 | Far infrared ray emitting polyester staple fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02160921A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1197588A1 (en) * | 2000-10-16 | 2002-04-17 | Degussa AG | The kinds of glycols starting material containing dispersed superfine ceramic powders coagulates capable of forming polyester molded body having high mechanical strength and transparency |
| EP1199389A1 (en) * | 2000-10-16 | 2002-04-24 | Degussa AG | Ethylene glycol dispersion containing ceramic nanoparticle agglomerates suitable for production of high-strength and high-transparence polyester molded article |
| JP2002180333A (en) * | 2000-12-11 | 2002-06-26 | Toray Ind Inc | Polyester staple fiber having latent crimp development and method for producing the same |
| KR100450530B1 (en) * | 2001-11-15 | 2004-09-30 | 주식회사 휴비스 | Method for producing functional polyester fiber |
| KR100467101B1 (en) * | 2001-08-13 | 2005-01-24 | 김희삼 | A manufacturing method of man made fiber and nonwoven fabric to use illite |
| CN100344804C (en) * | 2003-12-25 | 2007-10-24 | 纳米科技国际集团有限公司 | Bioactive nanofibers and their products |
| CN102560732A (en) * | 2011-12-16 | 2012-07-11 | 杭州贝斯特化纤有限公司 | Manufacturing technology for far-infrared polyester short fibers |
| US20210277592A1 (en) * | 2020-03-03 | 2021-09-09 | David HORINEK | Methods and compositions for manufacturing low thermal conductivity textiles |
-
1988
- 1988-12-13 JP JP63314325A patent/JPH02160921A/en active Pending
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1197588A1 (en) * | 2000-10-16 | 2002-04-17 | Degussa AG | The kinds of glycols starting material containing dispersed superfine ceramic powders coagulates capable of forming polyester molded body having high mechanical strength and transparency |
| EP1199389A1 (en) * | 2000-10-16 | 2002-04-24 | Degussa AG | Ethylene glycol dispersion containing ceramic nanoparticle agglomerates suitable for production of high-strength and high-transparence polyester molded article |
| JP2002180333A (en) * | 2000-12-11 | 2002-06-26 | Toray Ind Inc | Polyester staple fiber having latent crimp development and method for producing the same |
| KR100467101B1 (en) * | 2001-08-13 | 2005-01-24 | 김희삼 | A manufacturing method of man made fiber and nonwoven fabric to use illite |
| KR100450530B1 (en) * | 2001-11-15 | 2004-09-30 | 주식회사 휴비스 | Method for producing functional polyester fiber |
| CN100344804C (en) * | 2003-12-25 | 2007-10-24 | 纳米科技国际集团有限公司 | Bioactive nanofibers and their products |
| CN102560732A (en) * | 2011-12-16 | 2012-07-11 | 杭州贝斯特化纤有限公司 | Manufacturing technology for far-infrared polyester short fibers |
| US20210277592A1 (en) * | 2020-03-03 | 2021-09-09 | David HORINEK | Methods and compositions for manufacturing low thermal conductivity textiles |
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