JPH0631439B2 - Method for producing natural leather having far infrared radiation characteristics - Google Patents
Method for producing natural leather having far infrared radiation characteristicsInfo
- Publication number
- JPH0631439B2 JPH0631439B2 JP5939388A JP5939388A JPH0631439B2 JP H0631439 B2 JPH0631439 B2 JP H0631439B2 JP 5939388 A JP5939388 A JP 5939388A JP 5939388 A JP5939388 A JP 5939388A JP H0631439 B2 JPH0631439 B2 JP H0631439B2
- Authority
- JP
- Japan
- Prior art keywords
- far
- natural leather
- infrared radiation
- emissivity
- ceramics
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000010985 leather Substances 0.000 title claims description 43
- 230000005855 radiation Effects 0.000 title claims description 29
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000000919 ceramic Substances 0.000 claims description 44
- 239000002245 particle Substances 0.000 claims description 17
- 239000002270 dispersing agent Substances 0.000 claims description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 15
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 12
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 238000005470 impregnation Methods 0.000 description 8
- 238000009826 distribution Methods 0.000 description 7
- 239000000395 magnesium oxide Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 210000004209 hair Anatomy 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910052845 zircon Inorganic materials 0.000 description 4
- -1 zircon nitride nitride Chemical class 0.000 description 4
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 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 3
- 238000000295 emission spectrum Methods 0.000 description 3
- 229910052863 mullite Inorganic materials 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000017531 blood circulation Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 230000007721 medicinal effect Effects 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 229910052755 nonmetal Inorganic materials 0.000 description 2
- 150000002843 nonmetals Chemical class 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 229910000809 Alumel Inorganic materials 0.000 description 1
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 102000016942 Elastin Human genes 0.000 description 1
- 108010014258 Elastin Proteins 0.000 description 1
- 206010020565 Hyperaemia Diseases 0.000 description 1
- 206010020649 Hyperkeratosis Diseases 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
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- 229940037003 alum Drugs 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
- 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
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 description 1
- LBJNMUFDOHXDFG-UHFFFAOYSA-N copper;hydrate Chemical compound O.[Cu].[Cu] LBJNMUFDOHXDFG-UHFFFAOYSA-N 0.000 description 1
- 229910052878 cordierite Inorganic materials 0.000 description 1
- 230000035617 depilation Effects 0.000 description 1
- JSKIRARMQDRGJZ-UHFFFAOYSA-N dimagnesium dioxido-bis[(1-oxido-3-oxo-2,4,6,8,9-pentaoxa-1,3-disila-5,7-dialuminabicyclo[3.3.1]nonan-7-yl)oxy]silane Chemical compound [Mg++].[Mg++].[O-][Si]([O-])(O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2)O[Al]1O[Al]2O[Si](=O)O[Si]([O-])(O1)O2 JSKIRARMQDRGJZ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920002549 elastin Polymers 0.000 description 1
- 230000002708 enhancing effect Effects 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
- 230000000544 hyperemic effect Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- CNEOGBIICRAWOH-UHFFFAOYSA-N methane;molybdenum Chemical compound C.[Mo] CNEOGBIICRAWOH-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin 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
- 238000001931 thermography Methods 0.000 description 1
- 238000004861 thermometry Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 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
- 238000005406 washing Methods 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、人間が身に着ける靴、手袋、衣服や帽子等の
素材である天然皮革に遠赤外線放射エネルギーを放射せ
しめるようにした遠赤外線放射特性を有する天然皮革の
製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention relates to a far-infrared ray that radiates far-infrared ray radiant energy to natural leather which is a material for shoes, gloves, clothes, hats and the like worn by humans. The present invention relates to a method for producing natural leather having radiation characteristics.
[従来の技術] 従来、遠赤外線放射エネルギーを放射する天然皮革は全
く存在していなかった。[Prior Art] Conventionally, there has been no natural leather that radiates far infrared radiation energy.
[発明が解決しようとする課題] 前記の如く、従来は遠赤外線放射エネルギーを放射する
天然皮革は存在していなかったので、今迄のすべての天
然皮革は、遠赤外線放射特性を有していないために、遠
赤外線放射エネルギーが放射されず、従って遠赤外線の
照射によって得られる充血作用による血行の促進、保温
効果、新陳代謝の促進、その他医療効果や健康増進効果
を全く期待することができないという問題点があった。[Problems to be Solved by the Invention] As described above, since no natural leather that radiates far-infrared radiant energy has ever existed, all natural leathers up to now do not have far-infrared radiation characteristics. Therefore, far-infrared radiation energy is not radiated, so that it is not possible to expect any blood circulation promotion, heat retention effect, metabolism promotion, and other medical effects and health promotion effects due to the hyperemic action obtained by irradiation of far infrared rays. There was a point.
本発明は上記問題点を解決しようとする遠赤外線放射特
性を有する天然皮革の製造方法を提供せんとするもので
ある。The present invention is intended to provide a method for manufacturing natural leather having far-infrared radiation characteristics, which is intended to solve the above problems.
[課題を解決するための手段] 本発明は、30℃における遠赤外線放射率が波長4.5
〜30μmの領域で、平均65%以上である遠赤外線放
射特性を有するセラミックス粒子を、分散剤を用いて原
皮に含浸せしめるという製造方法を採用することによ
り、上記問題点を解決した。[Means for Solving the Problem] In the present invention, the far-infrared emissivity at 30 ° C. has a wavelength of 4.5.
The above problems were solved by adopting a manufacturing method of impregnating the raw leather with ceramic particles having a far infrared radiation property of which the average is 65% or more in the region of up to 30 μm.
[作用] 上記製造方法により製造された天然皮革に含浸したセラ
ミックスから常温でも遠赤外線放射エネルギーが放射さ
れるが、例えば前記天然皮革を靴に採用した場合、これ
を覆いて足の熱により靴内部が昇温すると更に放射率の
よい遠赤外線放射エネルギーがセラミックスから放射さ
れる。[Function] Far-infrared radiation energy is radiated from the ceramics impregnated in the natural leather manufactured by the above-described manufacturing method even at room temperature. For example, when the natural leather is applied to a shoe, it is covered with the heat of the foot inside the shoe. When the temperature rises, far-infrared radiation energy with better emissivity is emitted from the ceramics.
[実施例] 本発明製造方法に就いて説明するに、本発明は遠赤外線
放射特性を有するセラミックス粒子を天然皮革に分散剤
を用いて含浸せしめることを要旨とする。[Examples] To explain the production method of the present invention, the gist of the present invention is to impregnate ceramic particles having far-infrared radiation characteristics into natural leather with a dispersant.
すなわち、本発明は遠赤外線放射特性を有するセラミッ
クス粒子を天然皮革に含浸せしめることが必須の構成要
件であるので、最初に遠赤外線放射特性を有する物質に
ついて述べる。That is, in the present invention, it is essential that the natural leather is impregnated with the ceramic particles having the far-infrared radiation characteristic. Therefore, the substance having the far-infrared radiation characteristic will be described first.
遠赤外線放射特性を有する物質は種々あるが、本発明に
使用できる遠赤外線放射特性を有する物質は、30℃に
おける遠赤外線放射率が波長4.5〜30μmの領域で
平均65%以上であることが必要であり、好ましくは7
5%以上、特に好ましくは90%以上のものである。Although there are various substances having far-infrared emission characteristics, the substance having far-infrared emission characteristics that can be used in the present invention has a far-infrared emissivity at 30 ° C. of 65% or more on average in the wavelength range of 4.5 to 30 μm. Is required, preferably 7
It is 5% or more, and particularly preferably 90% or more.
遠赤外線放射特性を有する物質としては、酸化物系セラ
ミックス、非酸化物系セラミックス、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(Al2O3)系、マグネシア(M
gO)系、ジルコニア(ZrO2)系の外、酸化チタン
(TiO2)、二酸化ケイ素(SiO2)、酸化クロム
(Cr2O3)、フェライト(FeO2,Fe
3O4)、スピネル(MgO・Al2O3)、セリウム
(CaO2)、バリウム(BaO)等があり、炭化物系
セラミックスとしては、炭化ホウ素(B4C)、炭化ケ
イ素(SiC)、炭化チタン(TiC)、炭化モリブデ
ン(MoC)、炭化タングステン(WC)等があり、窒
化物系セラミックスとしては、窒化ホウ素(BN)、窒
化アルミ(AlN)、窒化ケイ素(Si3N4)、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(Mo)、バナジウム(V)、白
金(Pt)、タンタル(Ta)、マンガン(Mn)、ニ
ッケル(Ni)、酸化銅(Cu2O)、酸化鉄(Fe2
O3)があり、合金としてはニクロム、カンタル、ステ
ンレス、アルメルがあり、また結晶としては雲母、蛍
石、方解石、明ばん、水晶等がある。Examples of the substance having far-infrared radiation characteristics include oxide-based ceramics, non-oxide-based ceramics, non-metals, metals, alloys and crystals. For example, as oxide-based ceramics, alumina (Al 2 O 3 ) -based, magnesia (M
gO) type, zirconia (ZrO 2 ) type, titanium oxide (TiO 2 ), silicon dioxide (SiO 2 ), chromium oxide (Cr 2 O 3 ), ferrite (FeO 2 , Fe)
3 O 4 ), spinel (MgO · Al 2 O 3 ), cerium (CaO 2 ), barium (BaO), and the like, and the carbide ceramics include boron carbide (B 4 C), silicon carbide (SiC), and carbon carbide. Titanium (TiC), molybdenum carbide (MoC), tungsten carbide (WC), etc. are available, and nitride ceramics include boron nitride (BN), aluminum nitride (AlN), silicon nitride (Si 3 N 4 ), and zircon nitride nitride. (ZrN) and the like, non-metals include carbon (C) and graphite, and metals include tungsten (W), molybdenum (Mo), vanadium (V), platinum (Pt), tantalum (Ta), manganese ( Mn), nickel (Ni), copper oxide (Cu 2 O), iron oxide (Fe 2
O 3 ), alloys include nichrome, canthal, stainless steel, and alumel, and crystals include mica, fluorite, calcite, alum, quartz, and the like.
第1図は遠赤外線放射率分布図である。曲線Aはアルミ
ナ系、曲線Bはマグネシア系、曲線Cはジルコニア系の
放射スペクトルであり、波長4.5〜30μmの領域で
平均放射率はいずれも75%以上で本発明に採用でき
る。また曲線Dは非酸化物である炭化物系セラミックス
の炭化ジルコン(ZrC)の放射スペクトルであり、ま
た曲線Eは同じく非酸化物である窒化系セラミックスの
窒化チタン(TiN)の放射スペクトルである。その平
均放射率は60%以下であり、本発明には単独では採用
できない。曲線Fは透明な石英セラミックスの放射スペ
クトルである。その平均放射率は40%以下であり本発
明に単独では採用できない。FIG. 1 is a far-infrared emissivity distribution map. Curve A is an alumina-based spectrum, curve B is a magnesia-based spectrum, and curve C is a zirconia-based radiation spectrum. The average emissivity is 75% or more in the wavelength region of 4.5 to 30 μm, which can be adopted in the present invention. Curve D is the emission spectrum of zircon carbide (ZrC) of non-oxide carbide ceramics, and curve E is the emission spectrum of titanium nitride (TiN) of non-oxide nitride ceramics. It has an average emissivity of 60% or less and cannot be used alone in the present invention. Curve F is the emission spectrum of transparent quartz ceramics. Its average emissivity is 40% or less and cannot be used alone in the present invention.
遠赤外線放射率は上記の如くスペクトルを測定すること
によって求めることができるが、放射率は物質及びその
純度、粒子粒径または結晶体系、正方、六方、単方、立
方、三方、斜方等により決まるものである。Far-infrared emissivity can be obtained by measuring the spectrum as described above, but emissivity depends on the substance and its purity, particle size or crystal system, tetragonal, hexagonal, unilateral, cubic, trigonal, orthogonal, etc. It is decided.
特に有用な遠赤外線放射特性を有するセラミックスとし
ては、アルミナ系、マグネシア系、ジルコニア系があ
る。これを更に細かく分類するとアルミナ系ではアルミ
ナ、ムライト、マグネシア系ではマグネシア、コージラ
イト、ジルコニア系ではジルコンサンド(ZrO2・S
iO2)、ジルコン(ZiO2)等が挙げられる。また
上記の群から選ばれた1種または2種以上のものを混合
使用することも有効であり、上記の群から選ばれた1種
または2種以上のものを混合使用することも有効であ
り、上記の群から選ばれた1種または2種以上のものと
他のセラミックス(例えば炭化物系セラミックス)とを
混合使用することも有効である。Alumina-based, magnesia-based, and zirconia-based ceramics are particularly useful ceramics having far-infrared radiation characteristics. If this is further subdivided, alumina and mullite are used for alumina, magnesia and cordierite for magnesia, and zircon sand (ZrO 2 · S for zirconia).
iO 2 ), zircon (ZiO 2 ) and the like. It is also effective to mix and use one kind or two or more kinds selected from the above group, and it is also effective to mix and use one kind or two or more kinds selected from the above group. It is also effective to use a mixture of one or more selected from the above groups and other ceramics (for example, a carbide-based ceramic).
複合セラミックスを併用した場合の放射率の例を第2図
に示す。第2図の曲線Gはジルコニア(ZrO2)と酸
化クロム(Cr2O3)を1/1で混合した複合セラミ
ックスの放射率を示し、また第2図の曲線Hはアルミナ
(Al2O3)とマグネシア(MgO)を1/1で混合
した複合セラミックスの放射率を示すが、いずれも本発
明に有用である。Fig. 2 shows an example of the emissivity when the composite ceramics are used together. A curve G in FIG. 2 shows the emissivity of the composite ceramic in which zirconia (ZrO 2 ) and chromium oxide (Cr 2 O 3 ) are mixed at 1/1, and a curve H in FIG. 2 shows alumina (Al 2 O 3). ) And magnesia (MgO) at a ratio of 1/1, the emissivity of the composite ceramics is shown, and both are useful in the present invention.
上記の如き遠赤外線放射特性を有する粒子の純度は高い
程好ましいことが多く、純度95%以上で高放射率が得
られることが多い。例えば第3図はアルミナの純度を夫
々95%(曲線I)と85%(曲線J)にした場合の放
射率を示し、また第4図はムライトの純度を夫々95%
(曲線K)と85%(曲線L)にした場合の放射率を示
し、いずれも純度の高い程放射率が高いことを示してい
る。The higher the purity of the particles having the far-infrared radiation characteristics as described above, the more preferable it is, and a high emissivity is often obtained when the purity is 95% or more. For example, FIG. 3 shows the emissivity when the purity of alumina is 95% (curve I) and 85% (curve J), and FIG. 4 shows the purity of mullite of 95%, respectively.
(Curve K) and 85% (curve L) show the emissivity, and the higher the purity, the higher the emissivity.
而して、前記したように特に本発明に採用できる遠赤外
線放射特性を有するセラミックス粒子としては、酸化物
系セラミックス中のアルミナ系、マグネシア系、ジルコ
ニア系であり、これらを単独で、或いは混合して使用す
ることが好ましい。Thus, as described above, the ceramic particles having far-infrared radiation characteristics that can be particularly adopted in the present invention are alumina-based, magnesia-based, and zirconia-based oxide-based ceramics, which may be used alone or in combination. It is preferable to use.
次に、これら好ましい遠赤外線放射特性を有するセラミ
ックス粒子を天然皮革に含浸させる工程について詳細に
説明する。Next, the step of impregnating the natural leather with the ceramic particles having the preferable far-infrared radiation characteristics will be described in detail.
先ず、第1工程は原皮の水漬け工程である。これは原皮
をドラム(パドル)を用いて15〜20℃の洗滌水中に
浸漬して、原皮に付着している汚物、剥皮された原皮を
保存するため食塩水槽中に浸漬されて原皮に含浸してい
る塩分および皮中の可水溶性蛋白質等を洗滌、除去、溶
出させ、吸水軟化させて生皮の状態にするのである。First, the first step is the step of soaking the raw hide in water. This is to immerse the hide in a washing water of 15 to 20 ° C. using a drum (paddle), and to soak dirt and peeled hide in the saline solution tank to preserve the hide and impregnate the hide. The salt content and water-soluble proteins in the skin are washed, removed, and eluted to absorb and soften the water to form a rawhide.
そして、前記第1工程で軟らかくなった原皮を裏うち機
にかけて、皮下結締組織、脂肪、肉片等を取り除き、遠
赤外線放射特性を有するセラミックス粒子の含浸を容易
にする第2工程である裏うち(フレッシング)工程に入
る。Then, the raw leather softened in the first step is applied to a backlining machine to remove the subcutaneous tightening tissue, fat, meat pieces and the like, which is a second step of facilitating the impregnation of the ceramic particles having the far-infrared radiation characteristics (backlining ( Enter the freshening process.
次に第2工程を経た原皮を前記遠赤外線放射特性を有す
るセラミックス粒子を混入した水溶液中に、獣毛を脱毛
する脱毛促進剤および前記セラミックス粒子の分散効果
を高める分散剤、特に限定する必要はないが好ましくは
アルキルベンゼンスルホン酸塩より成る分散剤を夫々混
入した溶液中に浸漬せしめて、遠赤外線放射特性を有す
るセラミックス粒子を原皮に含浸させるというセラミッ
クス粒子の第1次含浸工程である第3工程に入る。な
お、この第3工程に於けるセラミックス水溶液に於ける
セラミックスと分散剤の濃度は表1の第1次含浸工程の
濃度にすることが好ましい。Next, the raw leather that has undergone the second step is added to an aqueous solution in which the ceramic particles having the far-infrared radiation characteristics are mixed, and a hair removal accelerator for removing animal hair and a dispersant for enhancing the dispersion effect of the ceramic particles, which are not particularly limited. The third step, which is a primary impregnation step of ceramic particles, is to impregnate the raw leather with ceramic particles having far-infrared radiation characteristics by immersing in a solution in which dispersants each consisting of an alkylbenzene sulfonate are mixed. to go into. The concentrations of the ceramics and the dispersant in the aqueous ceramic solution in the third step are preferably the concentrations in the first impregnation step in Table 1.
そして、更に第3工程によって遠赤外線放射特性を有す
るセラミックス粒子を含浸せしめた原皮に残留付着した
細毛、根毛、肉片や油性分を除去する手作業の第4工程
であるあかだし工程を経た後、遠赤外線放射効率を良く
するため再び原皮を前記第3工程に於けると略同様の工
程であるセラミックス粒子の第2次含浸工程である第5
工程に入る。すなわち、この第2次含浸工程では前記第
1次含浸工程の溶液中に混入した脱毛促進剤は不要であ
り、その他のセラミックス粒子水溶液に於けるセラミッ
クスと分散剤の濃度は、前記表1の第2次含浸工程の濃
度にすることが推奨される。 Then, after further passing through a squeezing step which is a fourth step of manual work for removing fine hairs, root hairs, pieces of meat and oily matter remaining on the raw leather impregnated with the ceramic particles having the far-infrared radiation characteristics by the third step, In order to improve the far-infrared radiation efficiency, the second step is the second step of impregnating the raw leather again with the ceramic particles, which is substantially the same step as the third step.
Enter the process. That is, in this second impregnation step, the depilation promoter mixed in the solution of the first impregnation step is unnecessary, and the concentrations of the ceramics and the dispersant in the other aqueous solution of the ceramic particles are as shown in Table 1 above. It is recommended to use the concentration of the secondary impregnation step.
前記第5工程が終了すると、革製造に不必要なケラトー
ス、エラスチン、脂肪等を溶脱させるために、蛋白分解
酵素によって処理を行ない皮に柔軟性を与える第6工程
であるベーティング工程を経て、用途、目的に応じて夫
々クロムなめし、タンニンなめし等のなめし工程で処理
して皮革とするのである。Upon completion of the fifth step, the keratose, elastin, fat, etc., which are unnecessary for leather production, are treated with proteolytic enzymes in order to leach them, and then undergo a sixth step of imparting flexibility to the skin. Depending on the use and purpose, it is treated with a tanning process such as chrome tanning and tannin tanning to obtain leather.
[実験例] 本発明の実験例を下記に示す。Experimental Example An experimental example of the present invention is shown below.
厚さ1mmの豚皮を使用して下記の表2のテスト条件によ
り遠赤外線放射特性を有するセラミックスを含浸させ
た。なお、含浸時に於ける温度は常温で、用水の温度は
15℃であり、また豚皮は含浸液中に静置状態で含浸さ
せた。A pig skin having a thickness of 1 mm was used to impregnate a ceramic having far infrared radiation characteristics under the test conditions shown in Table 2 below. The temperature at the time of impregnation was room temperature, the temperature of the water used was 15 ° C., and the pork skin was impregnated in the impregnating solution in a stationary state.
上記テスト条件によってセラミックスを豚皮に含浸させ
た結果、1mm厚みの豚皮全部にセラミックスが含浸され
た。 As a result of impregnating the pig skin with the above-mentioned test conditions, the whole pig skin having a thickness of 1 mm was impregnated with the ceramic.
そして、上記豚皮(天然皮革)にセラミックスを含浸し
た皮革と、セラミックスを含浸していない普通の天然皮
革との重量変化と、サーモ計測での遠赤外線効果を比較
した処、下記の表3、表4の結果を得た。Then, the weight change between the leather in which the pig skin (natural leather) is impregnated with ceramics and the ordinary natural leather not impregnated with ceramics and the far-infrared effect in thermometry are compared. The results shown in Table 4 were obtained.
前記表3による本発明に係る天然皮革の重量変化は、セ
ラミックスの含浸による増分であり、また表4によるサ
ーモ計測はホットプレートの表温を33℃とし、その表
面に皮革をセットし、遠赤外線効果をサーモグラフィで
計測すると、温度差が1℃であった。これが遠赤外線効
果である。 The weight change of the natural leather according to the present invention according to the above Table 3 is an increment due to the impregnation of the ceramics, and the thermo measurement according to Table 4 is that the surface temperature of the hot plate is 33 ° C. and the leather is set on the surface of the far infrared ray. When the effect was measured by thermography, the temperature difference was 1 ° C. This is the far infrared effect.
更に、本発明に係る天然皮革と汎用の天然皮革の保温状
態をテストした保温状態比較図を第5図に示すが、図
中、Mが本発明に係る天然皮革、Nが汎用の天然皮革で
ある。なお、ここで「1クロー」とは、気温21℃で人
間が快適である保温力を表示するものである。そして、
第5図により本発明に係る天然皮革が汎用の天然皮革よ
り保温力が優れていることが判る。Furthermore, FIG. 5 shows a heat retention state comparison diagram in which the heat retention states of the natural leather according to the present invention and general-purpose natural leather were tested. In the figure, M is the natural leather according to the present invention and N is a general-purpose natural leather. is there. In addition, "1 claw" is here what displays the heat retention power which a person is comfortable at the temperature of 21 degreeC. And
It can be seen from FIG. 5 that the natural leather according to the present invention has a higher heat retention than general-purpose natural leather.
また、第6図は本発明に係る天然皮革と汎用の天然皮革
の放射率を示す分布図であり、図中Oが本発明の天然皮
革の放射率を示し、Pが汎用の天然皮革の放射率を示
し、本発明の天然皮革が遠赤外線放射率が優れているこ
とが判る。Further, FIG. 6 is a distribution chart showing the emissivity of the natural leather according to the present invention and general-purpose natural leather, in which O indicates the emissivity of the natural leather of the present invention, and P indicates the emissivity of general-purpose natural leather. The results show that the natural leather of the present invention has an excellent far-infrared emissivity.
[発明の効果] 本発明は上述のようであるから、本発明製造方法によっ
て得られた天然皮革は、遠赤外線放射特性を有するセラ
ミックス粒子が含浸されているので常温でも遠赤外線が
放射されるが、例えばこれを靴に採用した場合、これを
履くと足の熱により靴の内部が昇温すると更に放射率の
よい遠赤外線放射エネルギーがセラミックスから放射さ
れ、その結果充血作用による血行の促進、保温効果、新
陳代謝の促進、その他医療効果や健康増進効果を期待す
ることができ、特に本発明に係る天然皮革は人間が身に
着ける前記靴の外、手袋、衣服や帽子に採用することに
より、その遠赤外線放射エネルギー効果を充分に利用す
ることができる。[Advantages of the Invention] Since the present invention is as described above, since the natural leather obtained by the production method of the present invention is impregnated with the ceramic particles having far-infrared radiation characteristics, far-infrared radiation is emitted even at room temperature. For example, when this is applied to shoes, if the temperature of the inside of the shoes rises when the shoes are worn, far infrared radiant energy with better emissivity is radiated from the ceramics, and as a result, blood circulation is promoted and heat retention due to hyperemia. Effects, promotion of metabolism, other medical effects and health promotion effects can be expected, and in particular, the natural leather according to the present invention is applied to the outside of the shoes worn by humans, gloves, clothes and hats, The far infrared radiation energy effect can be fully utilized.
【図面の簡単な説明】 第1図はセラミックスの遠赤外線放射率を示す分布図、
第2図は複合セラミックスの放射率を示す分布図、第3
図はアルミナの放射率を示す分布図、第4図はムライト
の放射率を示す分布図、第5図は本発明に係る天然皮革
と汎用の天然皮革との保温状態比較図、第6図は本発明
に係る天然皮革と汎用の天然皮革の放射率を示す分布図
である。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a distribution chart showing the far infrared emissivity of ceramics,
Fig. 2 is a distribution chart showing the emissivity of composite ceramics, and Fig. 3
FIG. 4 is a distribution chart showing the emissivity of alumina, FIG. 4 is a distribution chart showing the emissivity of mullite, FIG. 5 is a heat retention state comparison diagram of the natural leather according to the present invention and general-purpose natural leather, and FIG. 6 is It is a distribution diagram which shows the emissivity of the natural leather which concerns on this invention, and a general-purpose natural leather.
Claims (1)
5〜30μmの領域で、平均65%以上である遠赤外線
放射特性を有するセラミックス粒子を、分散剤を用いて
原皮に含浸せしめることを特徴とする遠赤外線放射特性
を有する天然皮革の製造方法。1. The far infrared emissivity at 30 ° C. has a wavelength of 4.
A method for producing a natural leather having far-infrared radiation characteristics, which comprises impregnating a raw leather with ceramic particles having a far-infrared radiation characteristic of 65% or more in an area of 5 to 30 μm using a dispersant.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5939388A JPH0631439B2 (en) | 1988-03-15 | 1988-03-15 | Method for producing natural leather having far infrared radiation characteristics |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5939388A JPH0631439B2 (en) | 1988-03-15 | 1988-03-15 | Method for producing natural leather having far infrared radiation characteristics |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01234500A JPH01234500A (en) | 1989-09-19 |
| JPH0631439B2 true JPH0631439B2 (en) | 1994-04-27 |
Family
ID=13111997
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5939388A Expired - Lifetime JPH0631439B2 (en) | 1988-03-15 | 1988-03-15 | Method for producing natural leather having far infrared radiation characteristics |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0631439B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01259100A (en) * | 1988-04-07 | 1989-10-16 | Toray Ind Inc | Composite leather |
| KR100390621B1 (en) * | 2001-04-06 | 2003-07-07 | 조광피혁 주식회사 | method for producting the leather emitting far infrared ray |
| KR100489725B1 (en) * | 2002-06-24 | 2005-05-16 | 박주민 | The processing method of natural leather |
-
1988
- 1988-03-15 JP JP5939388A patent/JPH0631439B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01234500A (en) | 1989-09-19 |
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