JPH03137274A - Heat insulating material - Google Patents
Heat insulating materialInfo
- Publication number
- JPH03137274A JPH03137274A JP1276252A JP27625289A JPH03137274A JP H03137274 A JPH03137274 A JP H03137274A JP 1276252 A JP1276252 A JP 1276252A JP 27625289 A JP27625289 A JP 27625289A JP H03137274 A JPH03137274 A JP H03137274A
- Authority
- JP
- Japan
- Prior art keywords
- inorganic compound
- alumina
- core
- magnesia
- sheath
- 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
- 239000011810 insulating material Substances 0.000 title abstract 2
- 239000000835 fiber Substances 0.000 claims abstract description 32
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims abstract description 25
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000002245 particle Substances 0.000 claims abstract description 21
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 17
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 14
- 239000000057 synthetic resin Substances 0.000 claims abstract description 14
- 239000000919 ceramic Substances 0.000 claims abstract description 13
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 13
- 239000000395 magnesium oxide Substances 0.000 claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000010030 laminating Methods 0.000 claims abstract description 4
- 150000004767 nitrides Chemical class 0.000 claims abstract description 4
- 239000002131 composite material Substances 0.000 claims description 19
- 230000000694 effects Effects 0.000 abstract description 12
- 230000035699 permeability Effects 0.000 abstract description 4
- 239000004814 polyurethane Substances 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 229920002647 polyamide Polymers 0.000 abstract description 3
- 229920002635 polyurethane Polymers 0.000 abstract description 3
- 108010020346 Polyglutamic Acid Proteins 0.000 abstract description 2
- 229920000370 gamma-poly(glutamate) polymer Polymers 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract 2
- 229910052576 carbides based ceramic Inorganic materials 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 26
- 239000004744 fabric Substances 0.000 description 17
- 239000000126 substance Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000005871 repellent Substances 0.000 description 6
- 229910026551 ZrC Inorganic materials 0.000 description 5
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- -1 polyethylene Polymers 0.000 description 5
- 230000002940 repellent Effects 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000009991 scouring Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052755 nonmetal Inorganic materials 0.000 description 2
- 150000002843 nonmetals Chemical class 0.000 description 2
- 229910052574 oxide ceramic Inorganic materials 0.000 description 2
- 239000011224 oxide ceramic Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229910000809 Alumel Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229910014813 CaC2 Inorganic materials 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- IAQWMWUKBQPOIY-UHFFFAOYSA-N chromium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Cr+4] IAQWMWUKBQPOIY-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000008821 health effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910000953 kanthal Inorganic materials 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- CNEOGBIICRAWOH-UHFFFAOYSA-N methane;molybdenum Chemical compound C.[Mo] CNEOGBIICRAWOH-UHFFFAOYSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920006264 polyurethane film Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000000191 radiation effect Effects 0.000 description 1
- 239000000941 radioactive substance Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- ZVWKZXLXHLZXLS-UHFFFAOYSA-N zirconium nitride Chemical compound [Zr]#N ZVWKZXLXHLZXLS-UHFFFAOYSA-N 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
- Woven Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は衣料等に用いて好適な保温性素材に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to a heat-retaining material suitable for use in clothing and the like.
(従来の技術)
従来主としてスポー゛ン衣料用に使用されている保温性
布帛としては織物や編物にポリウレタンやアクリル系樹
脂をコーティングしたり、樹脂皮膜をラミネートものが
使用されていた。また昨今では特公昭60−47954
号公報や特公昭6047955号公報で提案されている
湿式多孔膜による透湿防水布も知られている。また特開
昭584873号公報や特開昭59−100775号公
報ではSiO□多孔粒子を含むポリウレタン皮膜を布帛
」−に形成させる方法が開示されている。(Prior Art) Conventionally, heat-retaining fabrics mainly used for sports clothing have been woven or knitted fabrics coated with polyurethane or acrylic resin, or laminated with a resin film. Also, recently, special public service No. 60-47954
Moisture permeable waterproof fabrics using wet porous membranes proposed in Japanese Patent Publication No. 6047955 are also known. Further, JP-A-584-873 and JP-A-59-100775 disclose a method of forming a polyurethane film containing SiO□ porous particles on a fabric.
これらは機能として透湿性と防水性を同時に付与せしめ
たものである。さらにフィブリル化4弗化エチレン皮膜
を布帛上に貼伺した製品も使用されている。これらはい
ずれも透湿防水布としての機能のほかに保′/IA機能
を持っている。しかしこれらは体温が外気中に逃げるの
を防くという言わば消極的な意味での保温性である。These have both moisture permeability and waterproof properties. Furthermore, products in which a fibrillated tetrafluoroethylene film is applied to a fabric are also used. All of these have an insulation/IA function in addition to the function as a moisture-permeable waterproof fabric. However, these are heat retaining properties in the passive sense of preventing body heat from escaping into the outside air.
またアルミ扮をコーティング樹脂中に分散混入せしめて
体温の外気への放射を防ぐ方法や、炭化ジルコニウム等
の遠赤外線放射性物質をコーディング樹脂中に分散せし
めた製品も知られている。Also known are methods in which aluminum is dispersed in coating resin to prevent body heat from radiating into the outside air, and products in which far-infrared radioactive substances such as zirconium carbide are dispersed in coating resin.
(特開昭63−35887号公報、特開昭646857
2号公報、実開昭63−14.5894号公報)
一方、繊維中に遠赤外線放射性物質を含有せしめたもの
が特開昭63−92720号公報等に開示されている。(JP-A-63-35887, JP-A-646857)
(Japanese Unexamined Patent Publication No. 63-14.5894) On the other hand, JP-A No. 63-92720 and the like disclose fibers containing far-infrared emitting substances.
(発明が解決しようとする課題)
しかしながら、種々のコーティングを行う前記従来技術
は、多少の遠赤外線放射効果は認められるものもあるも
のの、実用上保温効果が不足しているのみならず、美観
上も問題のあるものが散見される。又、遠赤外線放射性
繊維は保温効果は認められるものの十分とは言い難いも
のである。(Problems to be Solved by the Invention) However, although the above-mentioned conventional techniques in which various coatings are applied have some degree of far-infrared radiation effect, they not only lack practical heat retention effects, but also have aesthetic problems. Problematic items are also found here and there. Further, although far-infrared emitting fibers have a heat-retaining effect, it is difficult to say that the effect is sufficient.
本発明の目的は着用時に優れた保温性と、熱源から効率
良く熱を吸収する快適な新規防寒衣料用の繊維素材を提
供するにある。An object of the present invention is to provide a new fiber material for cold-weather clothing that has excellent heat retention properties when worn and is comfortable and efficiently absorbs heat from a heat source.
(課題を解決するための手段)
本発明は、アルミナ、ジルコニア、マグネシア、酸化チ
タンの群から選ばれた無機化合物の粒子を含有するポリ
マーを芯部に配した芯鞘型複合繊維を用いた繊維構造物
からなる基材層、アルミナ、ジルコニア、マグネシア、
酸化チタン、炭化系セラミックス、窒化系セラミックス
の群から選ばれた無機化合物の粒子を含有する合成樹脂
皮膜層、及び透湿性を有するトップコート層を順次積層
してなる保温性素材である。(Means for Solving the Problems) The present invention provides a fiber using a core-sheath composite fiber in which a polymer containing particles of an inorganic compound selected from the group of alumina, zirconia, magnesia, and titanium oxide is disposed in the core. Base material layer consisting of a structure, alumina, zirconia, magnesia,
It is a heat-retaining material made by sequentially laminating a synthetic resin film layer containing particles of an inorganic compound selected from the group of titanium oxide, carbide ceramics, and nitride ceramics, and a moisture-permeable top coat layer.
本発明に使用される芯鞘型複合繊維はポリアミド、ポリ
エステル、ポリアクリルニトリル、ポリエチレン等が使
用できるが、耐熱性や合成樹脂皮膜層への染料の移行昇
華性の点から、ポリアミドが好適である。The core-sheath type composite fiber used in the present invention can be made of polyamide, polyester, polyacrylonitrile, polyethylene, etc., but polyamide is preferable from the viewpoint of heat resistance and sublimation property of dye transfer to the synthetic resin film layer. .
芯部には遠赤外線放射性を有する粒子を配置する。この
理由は一般に遠赤外線放射性を有する物質は硬度が高く
、この粒子が繊維表面に露出していると繊維の製造工程
で糸が接触する紡糸機、延伸機、編機、織機、等の金属
部分やガイド類を著しく損傷し安定した生産を得ること
が事実上困難であるためこれらの粒子を芯部に配置し鞘
部には粒子を含まない部分を配置し製造工程中のトラブ
ルを回避するためである。Particles that emit far infrared rays are placed in the core. The reason for this is that substances that emit far-infrared rays generally have high hardness, and if these particles are exposed on the fiber surface, metal parts of spinning machines, drawing machines, knitting machines, looms, etc. that come into contact with the thread during the fiber manufacturing process In order to avoid problems during the manufacturing process, these particles are placed in the core and a part that does not contain particles is placed in the sheath. It is.
遠赤外線放射性のある粒子としては、一般に、酸化物系
セラミックス、非酸化系セラミックス、非金属、金属、
合金、結晶等が挙げられる。例えば、酸化物系セラミッ
クスとしてはアルミナ(An203)系、マグネシア(
MgO>系、ジルコニア(ZrO7)系、の他、酸化チ
タン(T i 02 ) 、二酸化ケイ素(Sing)
、酸化クロム(Cr20.) フェライト(FeO2F
e304) スピネル(MgO−A7!203)セリ
ウム(CaC2) バリウム(B a C)等があり、
炭化物系セラミックスとしては、炭化ホウ素(B4 C
)、炭化チタン(T i C) 、炭化ケイ素(S i
C) 、炭化モリブデン(MoC)、炭化タングステ
ン(WC) 、等があり、窒化系セラミックスとしては
、窒化ホウ素(BN)、窒化アルミニウム(AnN)、
窒化ゲイ素(S13N4)窒化ジルコン(ZrN)、等
があり、非金属としては炭素(C) グラファイトが
あり、金属としてはタングステン(W> モリブデン
(M o )バナジウム(V) 白金(Pt) タ
ンタル(Ta)、マンガン(M n ) ニッケル(
Ni)酸化銅(Cu20)、酸化鉄(Fe20.l)が
あり、合金としてはニクロム、カンタル、ステンレスス
チール、アルメルがあり、結晶としては雲母、蛍石、方
解石、名ばん、水晶等がある。Particles that emit far infrared rays generally include oxide ceramics, non-oxidation ceramics, nonmetals, metals,
Examples include alloys and crystals. For example, oxide ceramics include alumina (An203), magnesia (
MgO> type, zirconia (ZrO7) type, titanium oxide (T i 02 ), silicon dioxide (Sing)
, chromium oxide (Cr20.) ferrite (FeO2F
e304) Spinel (MgO-A7!203) Cerium (CaC2) Barium (B a C), etc.
As carbide ceramics, boron carbide (B4C
), titanium carbide (T i C), silicon carbide (S i
C), molybdenum carbide (MoC), tungsten carbide (WC), etc., and nitride ceramics include boron nitride (BN), aluminum nitride (AnN),
There are silicon nitride (S13N4), zirconium nitride (ZrN), etc. Nonmetals include carbon (C), graphite, and metals include tungsten (W> molybdenum (Mo), vanadium (V), platinum (Pt), tantalum ( Ta), manganese (M n ), nickel (
Ni) Copper oxide (Cu20) and iron oxide (Fe20.l) are available; alloys include nichrome, kanthal, stainless steel, and alumel; crystals include mica, fluorite, calcite, nameplate, and quartz.
これらの内で特に有用な特性を有する無機物質としては
、アルミナ系、ジルコニア系、マグネシア系、酸化チタ
ン系が挙げられ、本発明で用いる芯鞘型複合繊維にはこ
れらを用いる。アルミナ系ではアルミナ、ムライト、ジ
ルコニア系ではジルコンサイド(ZrOz ・5iO
z) ジルコン(Zi()z)等が特に有効であり、
これらは混合使用することも有用である。例えばジルコ
ニア(ZiO□)と酸化クロム(CrO2)の併用やア
ルミナ(Aβ203)とマグネシア(MgO)の併用も
有用である。Among these, inorganic substances having particularly useful properties include alumina-based, zirconia-based, magnesia-based, and titanium oxide-based inorganic substances, and these are used in the core-sheath type composite fiber used in the present invention. Alumina-based products include alumina and mullite, and zirconia-based products include zirconside (ZrOz ・5iO
z) Zircon (Zi()z) etc. are particularly effective,
It is also useful to use a mixture of these. For example, a combination of zirconia (ZiO□) and chromium oxide (CrO2) or a combination of alumina (Aβ203) and magnesia (MgO) is also useful.
とくに複合繊維の芯部に配合する無機物質は無色または
白色或はそれに近い色相のセラミックスが染色の発色性
や美的効果の上からは望ましい。In particular, as the inorganic substance blended into the core of the composite fiber, colorless or white ceramics or ceramics with a hue close to white are desirable from the viewpoint of color development and aesthetic effects of dyeing.
よって、保温効果及び美的効果の」二からはアルミナが
最も好適である。Therefore, alumina is most suitable from the viewpoint of heat retention effect and aesthetic effect.
これら複合繊維の芯部に含有する無機物質の平均粒径は
0.2〜1.5μmが好適である。1.5μm以」−の
場合は分散性が不良となり生産に支障があり逆に0.2
μm以下の場合は粒子の凝集が起こりやすく不都合なこ
とが多い。該無機物質の含有量は、複合繊維の芯成分ポ
リマーに対して10〜80重量%が好ましく、20〜7
0重量%が特に好ましい。無機物質は芯部に配するが、
少量、例えば10重■%以下であれば鞘部に添加しても
よい。The average particle diameter of the inorganic substance contained in the core of these composite fibers is preferably 0.2 to 1.5 μm. If it is 1.5 μm or more, the dispersibility will be poor and production will be hindered;
When the particle size is less than μm, particles tend to aggregate, which is often inconvenient. The content of the inorganic substance is preferably 10 to 80% by weight, and 20 to 7% by weight based on the core component polymer of the composite fiber.
Particularly preferred is 0% by weight. Inorganic substances are placed in the core,
A small amount, for example, 10% by weight or less, may be added to the sheath.
又、鞘部を易溶解ポリマーで形成し、複合繊維を繊維構
造物となした後に、該鞘部の一部又は全部を熔解除去す
ると、芯部の無機物質が露出してより表面に近づくため
好ましい。In addition, if a part or all of the sheath is melted and removed after the sheath is formed from an easily soluble polymer and the composite fiber is made into a fiber structure, the inorganic substance in the core is exposed and gets closer to the surface. preferable.
複合繊維の鞘部の厚みは10μ以下、好ましくは7μ以
下が好ましい。The thickness of the sheath portion of the composite fiber is preferably 10 μm or less, preferably 7 μm or less.
第5図〜第11図は本発明複合繊維の横断面の具体例を
示す説明図である。図において、1は遠赤外線放射層の
芯部を示し、2は鞘部を示ず。鞘部2のポリマーは遠赤
外線を吸収するから、鞘部2の厚みをできるだけ薄くす
ることが好ましく、通常は10μ以下、好まり、 <は
5μ以下、特に2μ以下にすることが望ましい。第7図
、第8図、第11図は、遠赤外線放射層の芯部1が複数
個の例であり、鞘部2の厚みが薄く、且つ鞘部2によっ
て、繊維全体の強度も保たれやすいので好ましいことが
多い。第9図〜第11図は中空部3を有している本発明
複合繊維の例であり、セラミックス層をできるだけ外層
に近づ&−する目的で好ましいことが多い。FIGS. 5 to 11 are explanatory diagrams showing specific examples of cross sections of the composite fiber of the present invention. In the figure, 1 indicates the core of the far-infrared emitting layer, and 2 does not indicate the sheath. Since the polymer of the sheath part 2 absorbs far infrared rays, it is preferable to make the thickness of the sheath part 2 as thin as possible, usually less than 10μ, preferably less than 5μ, especially preferably less than 2μ. Figures 7, 8, and 11 show examples in which the far-infrared emitting layer has a plurality of core parts 1, and the thickness of the sheath part 2 is thin, and the strength of the entire fiber is maintained by the sheath part 2. It is often preferred because it is easy. 9 to 11 show examples of composite fibers of the present invention having hollow portions 3, which are often preferred for the purpose of bringing the ceramic layer as close to the outer layer as possible.
本保温性素材は第1図にその横断面図を示した如く、三
層からなるが、その機材層(4)は、前記複合繊維を用
いた繊維構造物である。該繊維構造物は、シート状のも
のであれば織物、編物、不織布等特に限定されない。又
、複合線♀[:1、繊維構造物の全面に亘って均一に用
いられればよく、他繊維と混紡、交編織、交撚、混繊等
を行ってもよい。但し、複合繊維の比率は繊維構造物の
少なくとも50重量%程度あることが好ましい。As shown in the cross-sectional view of FIG. 1, this heat-retaining material consists of three layers, and the material layer (4) is a fibrous structure using the composite fibers described above. The fiber structure is not particularly limited as long as it is in the form of a sheet, such as woven fabric, knitted fabric, or nonwoven fabric. Further, the composite wire ♀[:1] may be used uniformly over the entire surface of the fiber structure, and may be blended with other fibers, mixed knitted and woven, mixed twisted, mixed fibers, etc. However, it is preferable that the proportion of composite fibers is at least about 50% by weight of the fiber structure.
かかる基材層(4)には、合成樹脂皮膜層(5)が積層
されている。合成樹脂皮膜層(5)に用いるポリマーと
しては、ポリウレタン、アクリレート化合物が好ましく
、これらを多孔質皮膜となすことが望ましい。A synthetic resin film layer (5) is laminated on the base material layer (4). As the polymer used for the synthetic resin film layer (5), polyurethane and acrylate compounds are preferred, and it is desirable to form a porous film using these.
合成樹脂皮膜層(5)に添加される無機化合物(6)ト
シては、前記の如き、アルミナ、ジルコニア、マグネシ
ア、酸化チタンに加えて炭化系セラミックス、窒化系セ
ラミックスが用い得る。これは、一般に合成樹脂皮膜層
(5)を有する面は、衣服の内側に使用される場合が多
いので、無機化合物(6)は、炭化ジルコニウム等の有
色化合物も好適に使用できるからである。As the inorganic compound (6) added to the synthetic resin film layer (5), in addition to alumina, zirconia, magnesia, and titanium oxide as described above, carbonized ceramics and nitrided ceramics can be used. This is because the surface having the synthetic resin film layer (5) is often used on the inside of clothing, and colored compounds such as zirconium carbide can also be suitably used as the inorganic compound (6).
これら無機化合物(6)は通常樹脂固形分に対して5〜
70重量%用いるとよい。These inorganic compounds (6) usually contain 5 to 50% of the solid content of the resin.
It is preferable to use 70% by weight.
無機化合物(6)粒子を含有する合成樹脂皮膜層(5)
の厚さは5〜1100pさらに望ましくは10〜50μ
mが良い。5μm以下では十分な保温効果が得られず、
100μm以上では風合が硬化したり透湿性が低下する
ため実用上不適当である。Synthetic resin film layer (5) containing inorganic compound (6) particles
The thickness is 5 to 1100p, more preferably 10 to 50μ
m is good. If it is less than 5μm, sufficient heat retention effect cannot be obtained,
If the thickness is 100 μm or more, the texture becomes hard and the moisture permeability decreases, so it is not suitable for practical use.
更に、無機化合物(6)の粒子を含有する合成樹脂皮膜
層(5)が直接表層に露出している場合は摩擦堅牢度に
支障があるためその」一部に透湿性を有するトップコー
ト層(7)例えば、ポリウレタンおよび又はポリグルタ
メート化合物からなる皮膜を設ける必要がある。またト
ップコート層(7)にはさらに美的効果を向上させるた
めにバール顔料やメタリック光沢を有する顔料等の粒子
(8)を配合することも可能である。Furthermore, if the synthetic resin film layer (5) containing particles of the inorganic compound (6) is directly exposed to the surface layer, the abrasion fastness will be affected. 7) For example, it is necessary to provide a coating consisting of polyurethane and/or polyglutamate compounds. Furthermore, particles (8) of a Burl pigment or a pigment with metallic luster can also be blended into the top coat layer (7) in order to further improve the aesthetic effect.
(実施例)
(実施例1)
6ナイロンボリマ一粉末60重量部に平均粒径が0.6
μmで純度99%以上のγ−アルミナ20重量部と、ポ
リエチレンワックス20重量部を混練りした混合物を加
え、混練り機を使用して混合ポリマーを得た。(Example) (Example 1) 60 parts by weight of nylon bolymer powder has an average particle size of 0.6
A mixture obtained by kneading 20 parts by weight of γ-alumina with a purity of 99% or more in μm and 20 parts by weight of polyethylene wax was added, and a mixed polymer was obtained using a kneader.
ついで溶融複合紡糸機により、混合ポリマーが芯に、6
ナイロンボリマーが鞘になる様な同心円状断面(体積比
1:1)の複合体とし、270℃でノズルから紡出し冷
却、オイリングを行ない0
800m/minで巻き取り、更に3.2倍に延伸した
。而して、70デニールで18フイラメントのマルチフ
ィラメント(単糸:約3.9デニール)とし、公知の方
法でサテン織物(目付90g/m2 )を得た。Then, using a melt composite spinning machine, the mixed polymer is made into a core with 6
A composite with a concentric cross section (volume ratio 1:1) made of nylon polymer as a sheath, spun from a nozzle at 270°C, cooled, oiled, wound at 0.800 m/min, and further increased by 3.2 times. Stretched. A multifilament (single yarn: approximately 3.9 denier) of 18 filaments with a 70 denier was obtained, and a satin fabric (basis weight: 90 g/m2) was obtained by a known method.
このサテン織物を精練ヒートセット後、酸性染料を用い
て染色し、乾燥後、弗素系撥水剤にて撥水加工を施した
。更にクツションナイフコータを使用して、
架橋剤 X0LTEX CL−15(同上)
3 〃水
40 〃の組成からなる樹脂をアンダ
ーコート層として形成せしめた。After scouring and heat setting, this satin fabric was dyed with an acid dye, dried, and then treated with a fluorine-based water repellent to make it water repellent. Furthermore, using a cushion knife coater, crosslinking agent X0LTEX CL-15 (same as above)
3 Water
A resin having a composition of 40 was formed as an undercoat layer.
メインコート層としてるよ
炭化ジルコニウム粉末
0
水
4011からなる混合樹脂をパイプドクターにて
固形分で30g/m”、厚さ35μに塗布した。Main coat layer: Zirconium carbide powder 0 Water
A mixed resin consisting of 4011 was applied using a pipe doctor to a solid content of 30 g/m'' and a thickness of 35 μm.
更に
雲母系パール化顔料(日本光研製) 2 〃を固形分
で10μmの厚さに塗布しトップコート層を形成せしめ
た後、160℃にて1分間ピンテンターを用いて熱処理
を行なった。Furthermore, a solid content of mica-based pearlized pigment (manufactured by Nihon Koken) 2 was applied to a thickness of 10 μm to form a top coat layer, followed by heat treatment at 160° C. for 1 minute using a pin tenter.
(比較例1)
実施例1に於ける同心円状断面の芯鞘構造糸をレギュラ
ー6ナイロン糸に換え70デニールで18フイラメント
のマルチフィラメントとし公知の方法でタフタ織物(目
付70g/m”)を得た。(Comparative Example 1) The core-sheath structure yarn with a concentric circular cross section in Example 1 was replaced with a regular 6 nylon yarn, and a 70 denier 18 filament multifilament was used to obtain a taffeta fabric (basis weight 70 g/m") using a known method. Ta.
このタフタ織物を実施例1と同様の方法で精練、ヒート
セント、染色、撥水加工、アンダーコートを行ない、実
施例1のメインコートの処方から炭化ジルコニウム粉末
を除いた混合樹脂にて同様に塗布し、トップコート層も
実施例1と同様の方法で行なった。This taffeta fabric was scoured, heat-scented, dyed, water-repellent treated, and undercoated in the same manner as in Example 1, and then coated in the same manner as in Example 1 with a mixed resin obtained by excluding the zirconium carbide powder from the main coat formulation. However, the top coat layer was also formed in the same manner as in Example 1.
(比較例2)
比較例1にて使用した6ナイロンのマルチフィラメント
を用いた他は、実施例1と同様のサテン織物を作り、精
練、ヒートセット、染色、撥水加工を実施した。(Comparative Example 2) A satin fabric similar to that of Example 1 was made except that the nylon 6 multifilament used in Comparative Example 1 was used, and scouring, heat setting, dyeing, and water repellent treatment were performed.
(実施例2)
ポリエチレンテレフタレートに、マグネシアとポリエチ
レンワックスを体積混合比1/1に混合したものを混練
り機で混練りしマグネシア混合比が15重量%の混合ポ
リマーを得た。(Example 2) A mixture of polyethylene terephthalate and magnesia and polyethylene wax at a volume mixing ratio of 1/1 was kneaded using a kneading machine to obtain a mixed polymer having a magnesia mixing ratio of 15% by weight.
この混合ポリマーを芯にソディウムソルホイソフタル酸
2.5 m o 1%を共重合したカチオン可染型ポリ
エステルを鞘にした体積I:1の同心円状複合糸(10
0d/24f)を得た。この複合糸を使用してフィルを
製織し精練、ヒートセント後苛;−1−ソーダを使用し
て10重量%の減量加工を実施した1、その後カチオン
染料と分散染料を用いて紺色に染色し乾燥後、実施例1
と同様の方法で撥水加工、アンダーコート、メインコー
ト、トップコート、熱処理を実施した。A concentric composite yarn with a volume of I:1 (10
0d/24f) was obtained. This composite yarn was used to weave and scouring the fill, and after heat-scenting, it was processed to reduce the weight by 10% by weight using soda. After drying, Example 1
Water repellent finishing, undercoat, main coat, top coat, and heat treatment were performed in the same manner as above.
各々の加工布を18℃の室内で15cm平方の枠にセン
トし5Qcmの距離から500ワツトの白熱電球で布の
裏面(コーテイング品は塗布面)に照射し測温センサー
で非照射面の温度を1分毎に測定した。Place each piece of fabric in a 15cm square frame in a room at 18℃, illuminate the back side of the fabric (coated side for coated items) with a 500 watt incandescent light bulb from a distance of 5Qcm, and measure the temperature of the non-irradiated side using a temperature sensor. Measurements were taken every minute.
結果は第1表の通りである。The results are shown in Table 1.
(比較例3)
実施例1で得られたサテン織物に公知の方法でヒートセ
ット、染色、撥水加工、アンダーコートを行い、実施例
1のメインコートの処方から、炭化ジルコニウム粉末を
除いた(残部は水)混合樹脂にて同様に塗布し、トップ
コート層も実施例1と同様の方法で塗布した。かかる加
工布を比較例1〜2と同様に温度を測定した。結果を第
1表に3
4
(発明の結果)
」二連の如く本発明は保温効果を有する芯鞘型繊維と布
帛の加工工程で更に特定の無機化合物の粒子を含有する
合成樹脂を塗布することによりその吸熱効果が更に高ま
りスポーツ衣料や、防寒衣料として機能性の高い好適な
素材を提供するものである。(Comparative Example 3) The satin fabric obtained in Example 1 was heat set, dyed, water repellent, and undercoated by a known method, and the zirconium carbide powder was removed from the main coat formulation of Example 1 ( The remaining part was water) A mixed resin was applied in the same manner, and a top coat layer was also applied in the same manner as in Example 1. The temperature of the processed cloth was measured in the same manner as in Comparative Examples 1 and 2. The results are shown in Table 1. 3 4 (Results of the Invention) As stated above, the present invention further coats a synthetic resin containing particles of a specific inorganic compound in the process of processing core-sheath type fibers and fabrics that have a heat-retaining effect. This further enhances the heat absorbing effect and provides a highly functional material suitable for sports clothing and cold weather clothing.
本発明において特にトツブコ−1・層を配するのは合成
樹脂の塗布面の摩擦堅牢性をせしめる効果があり、更に
透湿性をイ1与せしめるごとにより着用中のムレ感が解
消できる。Particularly in the present invention, the provision of the Totsubuko-1 layer has the effect of increasing the abrasion fastness of the synthetic resin coated surface, and further improves moisture permeability, thereby eliminating the feeling of stuffiness during wear.
本発明による素材は寒冷地に於ける使用に最適であり、
血流を促進し健康増進効果を得ることができる。The material according to the invention is ideal for use in cold regions,
It can promote blood flow and have health-promoting effects.
第1図は本保温性素材の横断面の説明図であり第2図は
本発明に用い得る芯鞘型複合繊維の横断面を示す説明図
である。
4・・・基材層、
5・・・合成樹脂皮膜層、
6
トソプコート。FIG. 1 is an explanatory view of a cross section of the present heat-retaining material, and FIG. 2 is an explanatory view of a cross section of a core-sheath type composite fiber that can be used in the present invention. 4... Base material layer, 5... Synthetic resin film layer, 6 Tosop coat.
Claims (1)
の群から選ばれた無機化合物の粒子を含有するポリマー
を芯部に配した芯鞘型複合繊維を用いた繊維構造物から
なる基材層、アルミナ、ジルコニア、マグネシア、酸化
チタン、炭化系セラミックス、窒化系セラミックスの群
から選ばれた無機化合物の粒子を含有する合成樹脂皮膜
層、及び透湿性を有するトップコート層を順次積層して
なる保温性素材。(1) A base material layer consisting of a fiber structure using a core-sheath type composite fiber in which a polymer containing particles of an inorganic compound selected from the group of alumina, zirconia, magnesia, and titanium oxide is arranged in the core, alumina, A heat-retaining material made by sequentially laminating a synthetic resin film layer containing particles of an inorganic compound selected from the group of zirconia, magnesia, titanium oxide, carbide ceramics, and nitride ceramics, and a moisture-permeable top coat layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1276252A JPH03137274A (en) | 1989-10-23 | 1989-10-23 | Heat insulating material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1276252A JPH03137274A (en) | 1989-10-23 | 1989-10-23 | Heat insulating material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03137274A true JPH03137274A (en) | 1991-06-11 |
Family
ID=17566833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1276252A Pending JPH03137274A (en) | 1989-10-23 | 1989-10-23 | Heat insulating material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03137274A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0519089U (en) * | 1991-02-28 | 1993-03-09 | 株式会社ビツグマリン | Wet suit |
JPH10168615A (en) * | 1996-12-02 | 1998-06-23 | Komine Auto Center:Kk | Cold-protective and wind-breaking clothing |
KR100782223B1 (en) * | 2006-02-06 | 2007-12-05 | 엘에스전선 주식회사 | Insulated electric wire with partial discharge resistance and composition for manufacturing the same |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62104974A (en) * | 1985-10-31 | 1987-05-15 | 帝人株式会社 | Production of heat insulating moisture permeable waterproof fabric |
JPS63203873A (en) * | 1987-02-16 | 1988-08-23 | 前田 信秀 | Far infrared ray radiant composite fiber |
JPS6468572A (en) * | 1987-09-08 | 1989-03-14 | Unitika Ltd | Heat insulating moisture pervious waterproof cloth |
-
1989
- 1989-10-23 JP JP1276252A patent/JPH03137274A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62104974A (en) * | 1985-10-31 | 1987-05-15 | 帝人株式会社 | Production of heat insulating moisture permeable waterproof fabric |
JPS63203873A (en) * | 1987-02-16 | 1988-08-23 | 前田 信秀 | Far infrared ray radiant composite fiber |
JPS6468572A (en) * | 1987-09-08 | 1989-03-14 | Unitika Ltd | Heat insulating moisture pervious waterproof cloth |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0519089U (en) * | 1991-02-28 | 1993-03-09 | 株式会社ビツグマリン | Wet suit |
JPH10168615A (en) * | 1996-12-02 | 1998-06-23 | Komine Auto Center:Kk | Cold-protective and wind-breaking clothing |
KR100782223B1 (en) * | 2006-02-06 | 2007-12-05 | 엘에스전선 주식회사 | Insulated electric wire with partial discharge resistance and composition for manufacturing the same |
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