JP2018168518A5 - - Google Patents
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- JP2018168518A5 JP2018168518A5 JP2017069379A JP2017069379A JP2018168518A5 JP 2018168518 A5 JP2018168518 A5 JP 2018168518A5 JP 2017069379 A JP2017069379 A JP 2017069379A JP 2017069379 A JP2017069379 A JP 2017069379A JP 2018168518 A5 JP2018168518 A5 JP 2018168518A5
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- heat
- mass
- fiber
- less
- retaining
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- 239000000835 fiber Substances 0.000 description 7
- -1 polyethylene terephthalate Polymers 0.000 description 7
- 229920001155 polypropylene Polymers 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- XOLBLPGZBRYERU-UHFFFAOYSA-N Tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 4
- 238000005338 heat storage Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000006096 absorbing agent 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
- 238000009987 spinning Methods 0.000 description 3
- 230000005484 gravity Effects 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- PJXISJQVUVHSOJ-UHFFFAOYSA-N Indium(III) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 230000002087 whitening Effects 0.000 description 1
Description
しかしながら、十分な保温性を得るために特許文献1、2のように、酸化アンチモンをドーピングした酸化第二スズなどの無機微粒子を配合すると、繊維の比重が大きくなり、防寒衣料等が重量感のある衣料となり易い。
また、特許文献3の実施例記載のようなポリエチレンテレフタレートの中空繊維はポリエチレンテレフタレートの比重が1.38と高く、軽量性を向上させるために中空率を高くしているが、中空率が高い場合には、仮撚加工や撚糸等の工程で中空部の割れや潰れが生じるため、軽量性の付与には限界があった。
したがって、防寒衣料として十分な保温性を有し、かつ軽量である染色可能な蓄熱保温性繊維を得ることを目的としたものである。
However, when inorganic fine particles such as stannic oxide doped with antimony oxide are blended as in Patent Documents 1 and 2 in order to obtain sufficient heat retention, the specific gravity of the fiber increases, and the cold clothing and the like feel heavy. it easily becomes a certain clothing.
Further, the hollow fiber of polyethylene terephthalate as described in the examples of Patent Document 3 has a high specific gravity of 1.38 for polyethylene terephthalate, and the hollow ratio is increased in order to improve lightness, but the hollow ratio is high. However, since the hollow portion is cracked or crushed in a process such as false twisting or twisting, there is a limit to the provision of light weight.
Accordingly, the object is to obtain a dyeable heat-retaining heat-retaining fiber that has sufficient heat-retaining properties as a cold clothing and is lightweight.
赤外線吸収剤としては、例えば、アンチモンドープ酸化スズ(ATO)やスズドープ酸化インジウム(ITO)等が挙げられる。ATOの場合、ポリプロピレン樹脂に対し、2質量%以上、15質量%以下含有することが好ましい。含有量が2質量%未満であると十分な蓄熱保温性を得ることができず、15質量%を超えると紡糸時の曳糸性が極端に悪化する。あるいは、紡糸できても延伸工程での糸切れが生じ、さらには、延伸後の品質も満足できないものとなり易い。より好ましくは、3質量%以上、12質量%以下である。ITOの場合も、ATOと同様の割合で、ポリプロピレン樹脂に含有することが好ましい。 Examples of the infrared absorber include antimony-doped tin oxide (ATO) and tin-doped indium oxide (ITO). In the case of ATO , it is preferable to contain 2 mass% or more and 15 mass% or less with respect to polypropylene resin. Can not content to obtain sufficient heat storage insulation is less than 2 mass%, 15 mass% of spinnability at the time is exceeded and the spinning to extremely deteriorate. Alternatively, even if possible spinning occurs yarn breakage in the stretching step, further, it has easily become shall not be able to satisfy quality after stretching. More preferably, it is 3 mass% or more and 12 mass% or less. Also in the case of ITO , it is preferable to contain in a polypropylene resin in the same ratio as ATO .
赤外線吸収剤の粒子径としては、例えば、平均粒子径10μm以下であることが好ましい。平均粒子径が10μmを超えると紡糸フィルターの目詰まり、断糸等が生じ易くなる。より好ましくは、10nm以上、5μm以下であり、さらに好ましくは、10nm以上、3μm以下である。 The particle size of the infrared absorber is preferably, for example, an average particle size of 10 μm or less. Average the particle diameter exceeds 10μm clogging of the spinning filter, yarn breakage or the like occurs easily Kunar. More preferably, they are 10 nm or more and 5 micrometers or less, More preferably, they are 10 nm or more and 3 micrometers or less.
〔実施例1〕
ポリプロピレン樹脂(日本ポリプロ製「SA01A」、MFR9g/10min、融点164℃)に対して、赤外線吸収剤のアンチモンドープ酸化スズ(ATO)を4質量%添加したポリプロピレン樹脂を島成分に、ポリエチレンテレフタレート(融点258℃)を海成分に用い、海部:島部の面積比率が40:60となるように供給し、図1のように19個の島成分が繊維中央に配置される口金から288℃で紡出し、延伸倍率2.7倍で延伸し、3000m/minの速度で巻取り、67dtex/24fの蓄熱保温性繊維を得た。得られた蓄熱保温性繊維の繊維横断面における海部の最小厚みは1.2μmであり、海部と島部の界面での剥離は認められず、製糸安定性は良好であった。170℃で1分間の乾熱処理後も融着および溶断はなく耐熱性に優れたものであった。染色性は白化現象の発生がなく、密度も1.115g/cm3と軽量性に優れていた。また、蓄熱保温性評価ではATOを添加していないポリプロピレン樹脂を島成分に用いた以外は実施例1と同様の方法で作製した複合繊維を用いて得られた基準生地と比較して、照射10分後に+5.5℃、消灯1分後に+5.2℃と蓄熱保温性に優れていた。得られた結果を表1に示す。
[Example 1]
Polypropylene resin (“SA01A” manufactured by Nippon Polypro Co., Ltd., MFR 9 g / 10 min, melting point 164 ° C.) with 4 mass% of antimony-doped tin oxide (ATO) as an infrared absorber added to the island component, polyethylene terephthalate (melting point) 258 ° C) is used as a sea component, and the sea area: island area ratio is 40:60. As shown in FIG. 1, 19 island components are spun at 288 ° C. from a base disposed at the center of the fiber. It was taken out and drawn at a draw ratio of 2.7 times, and wound at a speed of 3000 m / min to obtain 67 dtex / 24 f of heat storage and heat retaining fiber. The minimum thickness of the sea part in the fiber cross section of the obtained heat-retaining and heat-retaining fiber was 1.2 μm, and no peeling at the interface between the sea part and the island part was observed, and the yarn production stability was good. Even after a dry heat treatment at 170 ° C. for 1 minute, there was no fusion and fusing, and the heat resistance was excellent. The dyeability was excellent in lightness with no whitening phenomenon and density of 1.115 g / cm 3 . Further, in the heat storage thermal insulation evaluated in comparison with a reference dough obtained by using the composite fibers prepared by the same method as in Example 1 except for using a polypropylene resin without added ATO to the island component, irradiated 10 The heat storage heat retention was excellent at + 5.5 ° C. after 1 minute and + 5.2 ° C. after 1 minute from extinction. The obtained results are shown in Table 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2017069379A JP7038481B2 (en) | 2017-03-30 | 2017-03-30 | Heat storage and heat retention fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2017069379A JP7038481B2 (en) | 2017-03-30 | 2017-03-30 | Heat storage and heat retention fiber |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2018168518A JP2018168518A (en) | 2018-11-01 |
JP2018168518A5 true JP2018168518A5 (en) | 2019-03-07 |
JP7038481B2 JP7038481B2 (en) | 2022-03-18 |
Family
ID=64019313
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2017069379A Active JP7038481B2 (en) | 2017-03-30 | 2017-03-30 | Heat storage and heat retention fiber |
Country Status (1)
Country | Link |
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JP (1) | JP7038481B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020054286A1 (en) | 2018-09-10 | 2020-03-19 | Agc株式会社 | Glass and laminated glass |
EP4212655A1 (en) * | 2020-09-07 | 2023-07-19 | Toray Industries, Inc. | Sea-island-type composite fiber, and fiber product including sea-island-type composite fiber |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60110920A (en) * | 1983-11-14 | 1985-06-17 | Kanebo Ltd | Electrically conductive composite fiber |
JPH01314716A (en) * | 1988-06-10 | 1989-12-19 | Unitika Ltd | White fabric having heat insulating property |
JP2824130B2 (en) * | 1989-07-25 | 1998-11-11 | 株式会社クラレ | Thermochromic composite fiber |
JPH03234819A (en) * | 1990-02-02 | 1991-10-18 | Toray Ind Inc | Lightweight sea-island conjugate type polyester yarn |
JP2002294520A (en) * | 2001-03-29 | 2002-10-09 | Kanebo Ltd | Luminous conjugated fiber |
JP2003027337A (en) * | 2001-07-18 | 2003-01-29 | Nippon Ester Co Ltd | Conjugate fiber having heat-storing and heat-retaining property |
JP2008240182A (en) * | 2007-03-27 | 2008-10-09 | Toray Ind Inc | Pile fabric and method for producing the same |
JP5661314B2 (en) * | 2010-03-30 | 2015-01-28 | 日本エステル株式会社 | Woven knitted fabric using core-sheath composite fiber yarn |
JP2014043659A (en) * | 2012-08-27 | 2014-03-13 | Toray Ind Inc | Sea-island type composite cross-section fiber and method for manufacturing the same |
JP2016069785A (en) * | 2014-09-30 | 2016-05-09 | Kbセーレン株式会社 | Core and sheath type composite fiber |
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2017
- 2017-03-30 JP JP2017069379A patent/JP7038481B2/en active Active
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