JPS63306036A - Heat-resistant refractory sheet - Google Patents
Heat-resistant refractory sheetInfo
- Publication number
- JPS63306036A JPS63306036A JP14171087A JP14171087A JPS63306036A JP S63306036 A JPS63306036 A JP S63306036A JP 14171087 A JP14171087 A JP 14171087A JP 14171087 A JP14171087 A JP 14171087A JP S63306036 A JPS63306036 A JP S63306036A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- layer
- sheet
- resistant
- water
- 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
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 20
- 239000000126 substance Substances 0.000 claims abstract description 15
- 239000000017 hydrogel Substances 0.000 claims description 23
- 230000009970 fire resistant effect Effects 0.000 claims description 19
- 230000002265 prevention Effects 0.000 claims description 5
- 239000010410 layer Substances 0.000 abstract description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 30
- 239000002893 slag Substances 0.000 abstract description 19
- 238000003466 welding Methods 0.000 abstract description 17
- 238000001704 evaporation Methods 0.000 abstract description 7
- 230000008020 evaporation Effects 0.000 abstract description 5
- 230000000717 retained effect Effects 0.000 abstract description 5
- 238000007789 sealing Methods 0.000 abstract description 5
- 239000000155 melt Substances 0.000 abstract description 3
- 238000002844 melting Methods 0.000 abstract description 3
- 230000008018 melting Effects 0.000 abstract description 3
- 239000002344 surface layer Substances 0.000 abstract description 2
- 230000002093 peripheral effect Effects 0.000 abstract 1
- 238000009834 vaporization Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 description 20
- 239000004744 fabric Substances 0.000 description 16
- 239000000835 fiber Substances 0.000 description 16
- 239000000499 gel Substances 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 11
- 239000011888 foil Substances 0.000 description 11
- 239000003365 glass fiber Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 229920000578 graft copolymer Polymers 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- -1 Locust Bingham Chemical compound 0.000 description 4
- 229920000049 Carbon (fiber) Polymers 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000004917 carbon fiber Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000035515 penetration Effects 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 230000009471 action Effects 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000010425 asbestos Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229920006037 cross link polymer Polymers 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- 229920000247 superabsorbent polymer Polymers 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- 239000005001 laminate film Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 229940014259 gelatin Drugs 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012210 heat-resistant fiber Substances 0.000 description 1
- 229910001385 heavy metal Chemical class 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、たとえば溶接・溶断作業中に飛散するスパッ
タ類から、床面あるいは当該作業現場近傍に存在する可
燃物や機材・機器等を保護し、あるいはバーナ類使用中
の火炎等による焼損や延焼等を防止するための防燃シー
トや防火カーテン、更には防音を兼ねた不燃シート等と
して使用される耐熱耐火シートに関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention protects combustible materials, materials, equipment, etc. existing on the floor or near the work site from spatter that is scattered during welding and fusing operations, for example. The present invention also relates to heat-resistant and fire-resistant sheets that are used as fire-proof sheets and fire-proof curtains to prevent burnout and spread of fire caused by flames during use of burners, and also as non-combustible sheets that also serve as soundproofing.
[従来の技術]
ガス溶接やシールドガス溶接等の溶接作業あるいは溶断
作業等においては、溶融金属(いわゆるノロ)の一部が
自重で下方に垂れ落ち、あるいはガス圧やアーク力等に
よりスパッタ等として溶接作業の周辺に飛散し、床面や
各種機器に焼損や熱損を及ぼすことがある。[Prior art] During welding work such as gas welding and shielding gas welding, or cutting work, a portion of molten metal (so-called slag) drips downward due to its own weight, or is spattered by gas pressure, arc force, etc. It may scatter around welding work and cause burnout and heat loss to the floor and various equipment.
こうした問題を防止する為、溶接作業現場の床面あるい
はその周辺に配置された各種材料や機器を耐熱耐火シー
トで保護する方法がとられており、かかる耐熱耐火シー
トとしてはガラス繊維布帛やカーボン繊維布帛等の耐熱
性布帛やアスベスト板あるいはこれらの耐熱性布帛の表
面にアルミニウム箔の如き金属箔や耐熱性合成樹脂層を
積層した複合シートや耐熱性合成樹脂を含浸した含浸シ
ート等が知られている。In order to prevent these problems, methods are used to protect various materials and equipment placed on or around the floor of welding work sites with heat-resistant and fire-resistant sheets. Such heat-resistant and fire-resistant sheets include glass fiber cloth and carbon fiber. Heat-resistant fabrics such as cloth, asbestos boards, composite sheets in which metal foil such as aluminum foil or heat-resistant synthetic resin layers are laminated on the surface of these heat-resistant fabrics, and impregnated sheets impregnated with heat-resistant synthetic resins are known. There is.
ところがこれら公知の耐熱耐火シートには次の様な難点
がある。However, these known heat-resistant and fire-resistant sheets have the following drawbacks.
■ガラス繊維やカーボン繊維単独では、1000℃を超
えることのあるノロが直接々触した場合に溶融若しくは
分解して貫通することがある。■Glass fibers or carbon fibers alone may melt or decompose and penetrate if they come into direct contact with slag, which can reach temperatures exceeding 1000°C.
■一般の有機質高分子を含浸させたものでは簡単に熱分
解を起こして発煙し、ときには有害ガスを発生すること
もあり、耐熱耐火シートとしての機能が発揮されていな
い。■Those impregnated with general organic polymers easily thermally decompose and emit smoke, sometimes emitting harmful gases, and do not function as heat-resistant and fire-resistant sheets.
■シリコーン樹脂の様な耐熱性樹脂を含浸させたもので
も完全不燃シートになる訳ではなく、着火、発煙を確実
に阻止することはできない。しかも素材的に見て非常に
高価であるので汎用性に欠ける。■Even sheets impregnated with heat-resistant resin such as silicone resin are not completely non-combustible and cannot reliably prevent ignition and smoke generation. Moreover, it is very expensive in terms of materials and lacks versatility.
■表面に金属箔を積層したシートの場合、輻射熱に対す
る若干の遮熱効果が得られる程度であって耐熱性向上効
果は殆ど期待できず、例えばノロ防護シートとして用い
た場合、ノロの保有熱で金属箔が簡単に溶融してシート
に貫通孔ができる。この場合金属自体による耐熱・耐火
性を得ようとすると相当厚肉の金属薄板を使用しなけれ
ばならず、そうなると金属薄板の柔軟性が乏しくなるの
で、各種機材・機器の防護シートとして使用する場合の
取り扱い示面倒であるばかりでなく、作業現場でのカッ
ティング等も困難である。■In the case of a sheet with metal foil laminated on its surface, it can only provide a slight heat shielding effect against radiant heat, and hardly any improvement in heat resistance can be expected.For example, when used as a slag protection sheet, the retained heat of slag The metal foil easily melts and creates through holes in the sheet. In this case, in order to obtain the heat resistance and fire resistance of the metal itself, it is necessary to use a fairly thick thin metal sheet, which makes the thin metal sheet less flexible, so when used as a protective sheet for various materials and equipment. Not only is it troublesome to handle, but it is also difficult to cut at the work site.
このほか、例えば特開昭49−39998号、同58−
97372号、同58−121970号などの公開公報
には、厨房火災の防止に用いる初期消火布として、繊維
基材に高吸水性高分子物質を含む含水ゲル(いわゆる水
ゲル)を含浸させたものが記載されている。この消火布
は、水ゲルの保有する水分の吸熱作用及び水分の蒸発に
よる吸熱作用を活用して耐熱性を高めたものであり、素
材自身の耐熱性を利用した従来の耐火シートとは若干異
質のものであると言える。In addition, for example, JP-A-49-39998, JP-A No. 58-
Publications such as No. 97372 and No. 58-121970 describe a fiber base material impregnated with a hydrogel (so-called water gel) containing a superabsorbent polymer substance as an initial fire extinguishing cloth used to prevent kitchen fires. is listed. This fire-fighting cloth has improved heat resistance by utilizing the heat-absorbing effect of water contained in water gel and the heat-absorbing effect of water evaporation, and is slightly different from conventional fire-resistant sheets that utilize the heat resistance of the material itself. It can be said that it belongs to
ところがこれらの水ゲル含浸消火布では、繊維基材にお
ける編目の比較的小さな隙間に水ゲルが含浸されただけ
のものであるから、全体としての保水量は必ずしも十分
であるとは言えず、たとえば天ぷら鍋等を火元とする比
較的低温の出火源に対してはそれなりの消火効果を発揮
し得るものの、これを溶接ノロの如< 1500℃以上
にも及ぶ高温物体からの断熱保護用として使用すると、
保水量の不足が直ちに吸熱作用(冷却作用)の不足とな
って現われ、高温物体の熱により水分が蒸発し、更に繊
維基材が焼失もしくは溶融して高温物体が貫通し断熱保
護効果を喪失する。However, in these water gel-impregnated fire extinguishing cloths, the water gel is only impregnated into relatively small gaps between the stitches in the fiber base material, so the overall water retention capacity cannot necessarily be said to be sufficient. Although it can exhibit a certain degree of extinguishing effect against relatively low-temperature fire sources such as deep fryers, it is not used for insulation protection from high-temperature objects such as welding slag that can reach temperatures exceeding 1500℃. When you use
Insufficient water retention immediately manifests as a lack of endothermic action (cooling action), and the water evaporates due to the heat of the high-temperature object, and the fiber base material is further burnt out or melted, allowing the high-temperature object to penetrate and lose its insulation protection effect. .
[発明が解決しようとする問題点]
本発明はこの様な事情に着目してなされたものであって
、その目的は、溶接ノロの様な高温の物体と接触した場
合でもその保有熱をすみやかに吸収して降温せしめ、高
温物体の貫通を生ずることなく優れた断熱保護効果を発
揮し得る様な耐熱耐火シートを提供しようとするもので
ある。[Problems to be Solved by the Invention] The present invention has been made with attention to these circumstances, and its purpose is to quickly dissipate retained heat even when it comes into contact with a high-temperature object such as welding slag. The object of the present invention is to provide a heat-resistant and fire-resistant sheet that absorbs heat and lowers the temperature of the object and exhibits an excellent heat-insulating protection effect without causing penetration of high-temperature objects.
[問題点を解決するための手段]
上記の目的を達成することのできた本発明シートの構成
は、高吸水性高分子物質を含む含水ゲル層の両面に、湿
潤した無機質繊維層が上記含水ゲル層と直接々触する様
に積層され、更に該積層物の両面は水分揮発防止フィル
ムで被覆されると共に、該水分揮発防止フィルムの周縁
がシールされたものであるところに要旨を有するもので
ある。[Means for Solving the Problems] The structure of the sheet of the present invention that has achieved the above object is that a wet inorganic fiber layer is formed on both sides of a hydrous gel layer containing a superabsorbent polymer substance. The gist is that the laminate is laminated so as to be in direct contact with the other layers, and both sides of the laminate are coated with a film to prevent moisture volatilization, and the periphery of the film to prevent moisture volatilization is sealed. .
[作用コ
本発明の耐熱耐火シートは、たとえば第1図(横断面拡
大模式図)に示す如く高吸水性高分子物質を含む含水ゲ
ル層1の両面に、湿潤した無機質繊維l1I2.2が含
水ゲル層1と直接々触する様に積層され、更に該積層物
の両面は水分揮発防止フィルム3.3で被覆されると共
に、該フィルム3.3の周縁をシールしてシート状の積
層物全体を密封したものであり、高熱の物体と接触した
ときの耐熱耐火機能は次の様にして発揮される。[Function] The heat-resistant and fire-resistant sheet of the present invention, for example, as shown in FIG. The laminate is laminated so as to be in direct contact with the gel layer 1, and both sides of the laminate are coated with a moisture volatilization prevention film 3.3, and the periphery of the film 3.3 is sealed to form the entire sheet-like laminate. The heat-resistant and fire-resistant function is demonstrated as follows when it comes into contact with a high-temperature object.
即ちたとえば第2図に示す如く、本発明のシートS上に
溶接ノロの様な高温物体Hが接触すると、表層部の水分
揮発防止フィルム3は直ちに焼失もしくは溶融し、高温
物体Hは耐熱性無機質繊維層2に接触することとなる。That is, as shown in FIG. 2, for example, when a high-temperature object H such as welding slag comes into contact with the sheet S of the present invention, the moisture volatilization prevention film 3 on the surface layer immediately burns out or melts, and the high-temperature object H is made of heat-resistant inorganic material. It will come into contact with the fiber layer 2.
この場合、無機質繊維のみからなる従来の耐火シートで
は、たとえガラス繊維やカーボン繊維等の耐熱性繊維か
らなるものであっても高温物体の熱で焼失もしくは溶融
して高温物体Hがシートの裏面側へ貫通し、また水ゲル
含浸シートを使用した場合でも、水分の保有量が十分で
ないため高温物体Hに対する玲却・降温効果は不十分で
あり、保有水分が蒸発した後も大量の熱が残ってその熱
が直接繊維基材に与えられて焼失もしくは溶融し、高温
物体Hはやはりシートの裏面側へ貫通してしまう。In this case, with conventional fire-resistant sheets made only of inorganic fibers, even if they are made of heat-resistant fibers such as glass fibers or carbon fibers, they are burned out or melted by the heat of the high-temperature object, and the high-temperature object H is exposed to the back side of the sheet. Even if a water gel-impregnated sheet is used, the cooling and cooling effect on the high-temperature object H is insufficient because it does not retain enough moisture, and a large amount of heat remains even after the retained moisture evaporates. The heat is applied directly to the fiber base material, burning it out or melting it, and the high-temperature object H also penetrates to the back side of the sheet.
これに対し本発明の耐熱耐火シートにおける無機質繊維
層2は湿潤状態に保たれているので、最初は高温物体H
の熱を受けて該繊維層2中の水分のみが蒸発するが、該
繊維層2の背面には大量の水分を保有する含水ゲル層2
が直接々触しているので、該繊維層2に存在している水
分が蒸発しても第2図に矢印で示す如く含水ゲル層2か
ら直ちに水分が補給されることになり、無機質繊維層2
は常時湿潤状態に保たれる。従って高温物体Hが相当の
熱量を保有するものであっても、含水ゲル層から補給さ
れる水分の蒸発熱によって確実に冷却される。その結果
、無機質繊維層2が保水量不足により昇温しで焼失した
り溶融する様な恐れはなくなる。On the other hand, since the inorganic fiber layer 2 in the heat-resistant and fire-resistant sheet of the present invention is kept in a moist state, the high-temperature object H
Only the moisture in the fiber layer 2 evaporates under the heat of
Since the fiber layer 2 is in direct contact with the inorganic fiber layer 2, even if the water present in the fiber layer 2 evaporates, water is immediately replenished from the hydrous gel layer 2 as shown by the arrow in FIG. 2
is kept constantly moist. Therefore, even if the high-temperature object H has a considerable amount of heat, it is reliably cooled by the heat of evaporation of the water replenished from the hydrous gel layer. As a result, there is no fear that the inorganic fiber layer 2 will burn out or melt due to an increase in temperature due to insufficient water retention.
即ち本発明では、高温物体の支持は湿潤状態の耐熱性無
機質繊維層2によって行なうこととし、高温物体Hの熱
により蒸発する水分の補給源として含水ゲルN1を組合
せることによって十分な保水量を確保し、高温物体Hを
急冷してその貫通を阻止するものである。That is, in the present invention, the high-temperature object is supported by the heat-resistant inorganic fiber layer 2 in a wet state, and a sufficient amount of water can be retained by combining the hydrogel N1 as a replenishment source for water that evaporates due to the heat of the high-temperature object H. This is to secure the high temperature object H and rapidly cool it to prevent it from penetrating.
また水分揮発防止フィルム3は保存時における水分の蒸
発を防止する機能を果たすものであり、積層物Sの周縁
部からの水分の揮発も防止するため、積層物Sの両面側
に被覆される該フィルム3は周縁で相互に接着しシール
されている。In addition, the moisture volatilization prevention film 3 has the function of preventing moisture from evaporating during storage, and also prevents moisture from evaporating from the periphery of the laminate S. The films 3 are glued and sealed together at their peripheries.
含水ゲル層1を構成する材料は、前述の説明からも明ら
かな様に大量の水を層状に保持し得るものでなければな
らず、高吸水性(本明細書では大量の水分を吸収して膨
潤し高粘性を与えるものを総称し、水分散性物質を含む
ものは含水ペースト状となるが、これも含水ゲルに包含
される)の高分子物質が用いられる。この様な高分子物
質としてはたとえば次の様なものが代表例として挙げら
れる。As is clear from the above description, the material constituting the hydrogel layer 1 must be capable of retaining a large amount of water in a layered manner, and must be highly absorbent (in this specification, it must be capable of absorbing a large amount of water). It is a general term for substances that swell and give high viscosity, and those containing water-dispersible substances become a water-containing paste, which is also included in the hydrogel). Representative examples of such polymeric substances include the following.
(天然高分子)
アルギン酸ソーダ、ゼラチン、大豆蛋白、植物蛋白、澱
粉、グアガム、アラビアゴム、トラガントゴム、寒天、
ローカストビンガム、カラギーナン、ペクチン、キチン
など、
(合成高分子)
ポリアクリル酸塩、ポリアクリルアミド、ポリ酢酸ビニ
ル加水分解物、ポリビニルピロリドン、メチルセルロー
ズ、カルボキシメチルセルローズ、ヒドロキシプロピル
メチルセルローズ、ポリエチレンオキサイド、あるいは
其他各種の高吸水性樹脂、たとえば澱粉系では、澱粉−
アクリロニトリルグラフト重合体、澱粉−アクリル酸グ
ラフト重合体、澱粉−スチレンスルホン酸グラフト重合
体、澱粉−ビニルスルホン酸グラフト重合体など:セル
ロース系では、セルロース−アクリロニトリルグラフト
重合体、セルロース−スチレンスルホン酸グラフト重合
体、カルボキシメチルセルロースの架橋重合体など:ポ
リビニルアルコール系では、ポリビニルアルコール架橋
重合体、アクリル−酢酸ビニルケン化物などニアクリル
系では、ポリアクリル酸塩架橋体、ポリアクリロニトリ
ル系重合体ケン化物など:ポリエチレンオキサイド系で
は、ポリエチレングリコールジアクリレート架橋重合体
など、
あるいはこあれらを基本ポリマーとする各種共重合体や
各種変性高分子等。(Natural polymers) Sodium alginate, gelatin, soy protein, vegetable protein, starch, guar gum, gum arabic, gum tragacanth, agar,
Locust Bingham, carrageenan, pectin, chitin, etc. (Synthetic polymers) Polyacrylate, polyacrylamide, polyvinyl acetate hydrolyzate, polyvinylpyrrolidone, methylcellulose, carboxymethylcellulose, hydroxypropylmethylcellulose, polyethylene oxide, or others For various super absorbent resins, such as starch-based resins, starch-
Acrylonitrile graft polymer, starch-acrylic acid graft polymer, starch-styrene sulfonic acid graft polymer, starch-vinyl sulfonic acid graft polymer, etc.: For cellulose, cellulose-acrylonitrile graft polymer, cellulose-styrene sulfonic acid graft polymer, etc. cross-linked polymers of carboxymethyl cellulose, etc.: Polyvinyl alcohol-based products include polyvinyl alcohol cross-linked polymers, acrylic-vinyl acetate saponified products, etc. Niacrylic-based products include polyacrylate cross-linked products, saponified polyacrylonitrile-based polymers, etc.: polyethylene oxide-based products Then, there are polyethylene glycol diacrylate cross-linked polymers, various copolymers and various modified polymers that use these as basic polymers, etc.
これらの高分子物質は単独で用いたり2 fi以上を混
合して使用し得る他、必要によってはキレート化剤、や
架橋性モノマー、天然もしくは合成の含水顆粒物等を併
用して粘性や形状保持性を更に高めることが可能である
。更に例えばベントナイトの如く水膨潤性の無機物質等
を加えて含水率や保形性等を高めたり、無機フィラー(
たとえば炭酸カルシウム、タルク、シリカ、アルミナ、
クレー、水酸化アルミニウム等)を少量加えることによ
ってゲル強度を高めたり、少量の高沸点溶剤を加えて水
分の蒸発を抑制し、更には防腐剤や紫外線吸収剤、凍結
防止剤等を微量混入して含水ゲル層の劣化や腐敗(殊に
粘度低下)を防止することも可能である。These polymeric substances can be used alone or in a mixture of 2 fi or more, and if necessary, they can be used in combination with chelating agents, crosslinking monomers, natural or synthetic water-containing granules, etc. to improve viscosity and shape retention. It is possible to further increase the Furthermore, water-swellable inorganic substances such as bentonite may be added to increase water content and shape retention, or inorganic fillers (
For example, calcium carbonate, talc, silica, alumina,
The strength of the gel is increased by adding a small amount of clay, aluminum hydroxide, etc., the evaporation of water is suppressed by adding a small amount of a high-boiling point solvent, and even small amounts of preservatives, ultraviolet absorbers, antifreeze agents, etc. are mixed in. It is also possible to prevent deterioration and putrefaction (particularly viscosity reduction) of the hydrogel layer.
尚これらの高分子物質によって構成される含水ゲル層は
、前述の如く無機繊維層へ水分を補給するための含水層
としての機能を果たすものであり、含水ゲル自体によっ
て層を構成するのが原則であるが、場合によっては繊維
密度の低い比較的厚肉の不織布マット等に含水ゲルを含
浸して保形性を高めることも可能である。The hydrogel layer composed of these polymeric substances functions as a hydrous layer for replenishing moisture to the inorganic fiber layer as described above, and in principle, the layer is composed of the hydrogel itself. However, in some cases, it is also possible to improve shape retention by impregnating a relatively thick nonwoven fabric mat with a low fiber density with a hydrogel.
次に上記含水ゲル層の両面に積層される耐熱性無機X*
維は、溶接ノロの様な高温物体を支持する主体となるば
か冷却用水の担持層としての機能を果たし、更には含水
ゲル層を背面側から支持する支持層としての効果も兼備
するものであり、繊維素材の具体例としては、ガラス繊
維、カーボン繊維、ロックウール繊維、アスベスト繊維
、金属繊維、セラミックス繊維等が挙げられ、これらは
混紡したものであフても、不織布状であっても勿論かま
わない。Next, heat-resistant inorganic X* is laminated on both sides of the hydrogel layer.
The fibers function as a support layer for cooling water, which is the main support for high-temperature objects such as welding slag, and also serve as a support layer to support the hydrous gel layer from the back side. Specific examples of fiber materials include glass fibers, carbon fibers, rock wool fibers, asbestos fibers, metal fibers, ceramic fibers, etc. These may be blended or non-woven. I don't mind.
また水分揮発防止用フィルムは、水分非透過性フィルム
である限り素材の種類は全く制限されないが、最も一般
的なものとしては、ポリエチレン、ポリプロピレン等の
ポリオレフィンの他、ポリ塩化ビニリデン、ポリエステ
ル、ナイロン等の合成樹脂あるいはアルミニウムやステ
ンレス等の金属箔、更にはそれらのラミネートフィルム
等が例示される。There are no restrictions on the type of material used for the film to prevent moisture volatilization, as long as it is moisture-impermeable, but the most common ones include polyolefins such as polyethylene and polypropylene, as well as polyvinylidene chloride, polyester, and nylon. Examples include synthetic resins, metal foils such as aluminum and stainless steel, and laminate films thereof.
尚金属箔や金属箔ラミネートフィルムを使用した場合は
、シートの外面が美麗な金属色を呈しているため外観が
良く、しかも輻射熱反射効果により断熱効果を更に高め
るといフた効果も発揮するので好ましい、但し溶接部近
辺で使用する場合は、輻射熱反射効果が災いして溶接作
業員へのいわゆる照り返しという障害をもたらすことも
あるので、この様な場合は金属箔の表面に粗面加工を施
したり艶消し塗料を塗布する等の処理を施しておくこと
が望まれる。When metal foil or metal foil laminate film is used, it is preferable because the outer surface of the sheet has a beautiful metallic color, which gives it a good appearance, and it also has the additional effect of further increasing the heat insulation effect by reflecting radiant heat. However, if it is used near a welding area, the radiant heat reflection effect may cause problems such as reflections on welding workers, so in such cases, the surface of the metal foil should be roughened or It is desirable to apply a treatment such as applying matte paint.
次に耐熱耐火シートの代表的な製法について説明する。Next, a typical manufacturing method for heat-resistant and fire-resistant sheets will be explained.
まず無機質繊維布2を構成する布状物の片面に水分揮発
防止用フィルム3を貼り合わせたものを2枚準備すると
共に、高吸水性高分子物質を大量(10〜200倍量程
度)の水に溶解・分散させて含水ゲルを調製する。そし
て上記貼り合わせ物の1枚を、布状物を上面にして平板
上に敷延し両側縁を若干持ち上げぎみにしておき、この
上に前述の含水ゲルを流延しあるいはロールコート法や
リバースコート法等により所定の厚さとなる様に塗布す
る。尚この塗布工程では、含水ゲルを50〜80℃にし
て粘度を低下せしめた状態で塗布し、その後冷却してゲ
ル状に固める方法を採用すれば、円滑な塗布作業性のも
とで均一な厚さの含水ゲル層1が得られる。また比較的
低粘度の水性高分子液として塗布した後、その上面にゲ
ル化剤をスプレー法等により供給してゲル化させる方法
を採用すれば、含水ゲル層形成−を比較的低粘度の状態
で塗布することができるので、含水ゲル層1の形成作業
性が良く且つ均一な厚さの含水ゲル層が得られ易い。First, two sheets of cloth-like material constituting the inorganic fiber cloth 2 are laminated with the film 3 for preventing moisture volatilization on one side, and a large amount of water (approximately 10 to 200 times the amount) of a super absorbent polymer material is prepared. Prepare a hydrogel by dissolving and dispersing it in Then, one sheet of the above-mentioned bonded material is spread on a flat plate with the cloth-like material facing upward, both edges of which are slightly raised, and the above-mentioned hydrogel is cast on top of this, or by roll coating or reverse coating. Apply to a predetermined thickness using a coating method or the like. In addition, in this application process, if a method is adopted in which the water-containing gel is applied after being heated to 50 to 80°C to reduce its viscosity, and then cooled and solidified into a gel-like state, uniform application can be achieved with smooth application workability. A thick hydrogel layer 1 is obtained. In addition, if a method is adopted in which a relatively low-viscosity aqueous polymer liquid is applied and then a gelling agent is applied to the top surface by a spray method or the like to gel it, a hydrogel layer can be formed in a relatively low-viscosity state. Since the hydrogel layer 1 can be coated with the same coating method, the formation workability of the hydrogel layer 1 is good and the hydrogel layer with a uniform thickness can be easily obtained.
ゲル化剤の種類は用いる高分子物質の種類に応じて選定
すべきであり、たとえば硼砂や硼酸カリウム等の硼酸塩
、アンチモン化合物、クロム酸塩、アルカリ金属、アル
カリ土類金属、銅族、鉄族等の各種金属塩や重金属塩、
各種の有機酸や無機酸、金属水酸化物や炭酸塩、アンモ
ニア、アミン等の各種アルカリ等が例示され、これらは
必要に応じ1種又は2種以上を組合せて使用される。The type of gelling agent should be selected depending on the type of polymer substance used, such as borates such as borax and potassium borate, antimony compounds, chromates, alkali metals, alkaline earth metals, copper group, iron. various metal salts and heavy metal salts such as
Examples include various organic acids and inorganic acids, metal hydroxides and carbonates, and various alkalis such as ammonia and amines, and these may be used alone or in combination of two or more as necessary.
含水ゲル層1の厚さは要求される耐熱耐火性の程度に応
じて調整し得るものであって格別の制限が課せられる訳
ではなく、例えば0.1〜10mm程度の範囲で任意に
変更することができる。The thickness of the hydrous gel layer 1 can be adjusted according to the required degree of heat and fire resistance, and there are no particular restrictions imposed on it, and it can be changed arbitrarily within the range of, for example, about 0.1 to 10 mm. be able to.
この様にして含水ゲル層1を形成した後は、先に準備し
ておいたもう1枚の貼り合わせ物(無機室繊維布2+水
分揮発防止フィルム3)を、無機質繊維布2を下にして
上記含水ゲル層1の上面に積層し、次いで該貼り合わせ
物の周縁をシールすることによって本発明の耐熱耐火シ
ートが得られる0周縁シールの方法も一切制限がなく、
ヒートシール性フィルムを用いたヒートシール法、粘着
剤やホットメルト接着剤等の接着剤を用いた接着シール
法等が、適宜採用される。尚無機質繊維布2は、上記製
造工程で含水ゲルFilから移行してくる水分によって
自然に潤滑状態となるが、必要によっては上記積層工程
に先立って水槽への浸漬、ロール付着、スプレー付着等
により無機質繊維布2を湿潤させておくこともできる。After forming the hydrogel layer 1 in this way, place the other bonded material prepared earlier (inorganic fiber cloth 2 + moisture volatilization prevention film 3) with the inorganic fiber cloth 2 facing down. The method of zero-periphery sealing, in which the heat-resistant and fire-resistant sheet of the present invention is obtained by laminating the above hydrogel layer 1 on the upper surface and then sealing the periphery of the bonded product, is not limited at all.
A heat-sealing method using a heat-sealable film, an adhesive sealing method using an adhesive such as an adhesive or a hot-melt adhesive, etc. are employed as appropriate. The inorganic fiber cloth 2 is naturally lubricated by the moisture transferred from the hydrous gel Fi in the above manufacturing process, but if necessary, it may be lubricated by immersion in a water tank, roll adhesion, spray adhesion, etc. prior to the above lamination process. The inorganic fiber cloth 2 can also be kept moist.
本発明の耐熱耐火シートは所定寸法の板状物として製品
化することも勿論可能であるが、生産工程の連続化及び
輸送、保存、使用時の便宜等を考えると最も好ましいの
は、適当な幅(例えば30Co1〜150cm程度)の
巻回可能な帯状物として製品化したものである。この場
合、たとえば第3図に示す如く長尺帯状シートの幅方向
及び/又は長手方向に適当な間隔で切断可能な分断用シ
ール部shを設けておけば、断熱保護面積に応じた広さ
のものに切断して使用することができるので極めて便利
である。It is of course possible to commercialize the heat-resistant and fire-resistant sheet of the present invention as a plate-like product of a predetermined size, but considering the continuity of the production process and the convenience of transportation, storage, and use, it is most preferable to use a suitable sheet. It is commercialized as a rollable band with a width (for example, about 30Co1 to 150cm). In this case, for example, as shown in Fig. 3, if a dividing seal part sh that can be cut at appropriate intervals in the width direction and/or length direction of the long strip sheet is provided, the width can be adjusted according to the heat insulation protection area. It is extremely convenient because it can be cut into pieces and used.
[実施例]
実施例1
ガラスisl維クロス(平織シート:厚さ0.2 +u
+)の裏面にアルミニウム箔をラミネートしてなる貼り
合わせシートを2枚準備し、該貼り合わせシートの1枚
をガラス繊維クロスを上面にして平板上に広げ、この上
に、ローカストビンガム5重量%を含む高粘性の高分子
水溶液を80′℃に加温した状態で厚さ2■となる様に
ナイフコート法により塗布する1次いで冷却し、プリン
状に固まった含水ゲルの上面に、先に準備上たもう1枚
の貼り合わせシートをガラス繊維クロスを下面にして重
ね合わせ、次いで上下の貼り合わせシートの周縁を、ア
ルミニウム箔にポリエチレンをラミネートしたフィルム
によってシールし、本発明の耐熱耐火シートを得た。[Example] Example 1 Glass ISL fiber cloth (plain weave sheet: thickness 0.2 +u
Prepare two laminated sheets made by laminating aluminum foil on the back side of +), spread one of the laminated sheets on a flat plate with the glass fiber cloth on top, and add 5% by weight of locust Bingham on top of this. A highly viscous polymeric aqueous solution containing 100% polyester is heated to 80'°C and coated using the knife coating method to a thickness of 2 cm.1st, it is cooled and the top surface of the hydrous gel, which has hardened into a pudding-like shape, is coated. In preparation, another laminated sheet is placed on top of the other with the glass fiber cloth facing down, and then the periphery of the upper and lower laminated sheets is sealed with a film made of aluminum foil laminated with polyethylene to form the heat-resistant and fire-resistant sheet of the present invention. Obtained.
この耐熱耐火シートを溶接試験台の下面(高さ10cm
)に敷延し、炭酸ガスアーク溶接(30cm幅で3往復
)を行ない、落下するノロを耐熱耐火シート上に受けた
ところ、ノロは水蒸気の蒸発と共に急冷され耐熱耐火シ
ートの燃焼及び貫通焼損は全く認められなかった。This heat-resistant fireproof sheet was placed on the underside of the welding test stand (height 10 cm).
), carbon dioxide gas arc welding (30cm width, 3 reciprocations) was carried out, and when the falling slag was caught on the heat-resistant fire-resistant sheet, the slag was rapidly cooled as the water vapor evaporated, and there was no burning or penetration burnout of the heat-resistant fire-resistant sheet. I was not able to admit.
実施例2
実施例1のローカストビンガム含有含水ゲルに代えて、
厚さ2mmの低密度のガラス繊維不織布にローカストビ
ンガム3重量%を含む高粘性高分子水溶液を含浸してな
る含水ゲル層構成材を使用した他は実施例1と同様にし
て耐熱耐火シートを得た。Example 2 Instead of the locust Bingham-containing hydrogel of Example 1,
A heat-resistant and fire-resistant sheet was obtained in the same manner as in Example 1, except that a hydrogel layer constituent material formed by impregnating a 2-mm-thick low-density glass fiber nonwoven fabric with a highly viscous polymer aqueous solution containing 3% by weight of locust Bingham was used. Ta.
このシートを実施例1と同様の耐火試験に付したところ
、燃焼及びノロの貫通は全く認められなかフた。When this sheet was subjected to the same fire resistance test as in Example 1, no combustion or slag penetration was observed.
比較例1
実施例1で使用したガラス繊維クロスのみを2枚積層し
て実施例1と同様の耐火試験に付したところ、大粒のノ
ロはもとより比較的小粒のノロが落下した部分でもガラ
ス繊維が溶融して貫通孔ができ、ノロは裏面側まで貫通
した。Comparative Example 1 When two sheets of only the glass fiber cloth used in Example 1 were laminated and subjected to the same fire resistance test as in Example 1, the glass fibers were found not only in large particles of slag but also in areas where relatively small particles had fallen. It melted, creating a through hole, and the slag penetrated all the way to the back side.
比較例2
上記と同じガラス繊維クロスに、ローカストビンガム3
重量%を含む粘性水溶液を含浸付着させ、両面に付着し
た粘稠物を除去した後、両面に実施例1で用いたのと同
じアルミニウム箔を貼合して耐火シートを得た。Comparative Example 2 Locust Bingham 3 was added to the same glass fiber cloth as above.
After impregnating and adhering a viscous aqueous solution containing % by weight and removing the viscous substance adhering to both sides, the same aluminum foil as used in Example 1 was laminated on both sides to obtain a fireproof sheet.
このシートを実施例1と同様に耐火試験に付したところ
、極く小さなノロの小粒やスパッターの貫通は阻止し得
るものの、中〜大粒のノロが落下した部分では瞬時に水
分が揮発すると共にガラス繊維が溶融して貫通孔ができ
、満足のいく保護効果は得られなかった。When this sheet was subjected to a fire resistance test in the same manner as in Example 1, it was found that although it was able to prevent the penetration of extremely small particles of slag and spatter, moisture instantly evaporated in areas where medium to large particles of slag had fallen, and the glass The fibers melted, creating through-holes, and a satisfactory protective effect could not be obtained.
【発明の効果]
本発明は以上の様に構成されており、その効果を要約す
ると次の通りである。[Effects of the Invention] The present invention is configured as described above, and its effects are summarized as follows.
■ノロ等の高温物質の保有する熱や火炎等による熱は、
無機質繊維層の保有する水分及び含水ゲル層から補給さ
れる水分の吸熱作用及び蒸発熱により奪われて急冷され
るので、無機質繊維層が過度に昇温して溶融する様な恐
れがなく、裏面側の床材や被保護材等を確実に保護する
ことができる。■The heat possessed by high-temperature substances such as slag and the heat caused by flames, etc.
Since the water contained in the inorganic fiber layer and the water replenished from the hydrous gel layer are taken away by the endothermic action and heat of evaporation and rapidly cooled, there is no risk of the inorganic fiber layer heating up excessively and melting. Side flooring and protected materials can be reliably protected.
■無機質繊維層への給水源となる含水ゲル層は、極めて
吸水率の高い高分子物質からなるものであって、極く少
量の高分子物質でその目的を果たすので、極めて安価に
提供することができる。■The water-containing gel layer, which serves as the water supply source to the inorganic fiber layer, is made of a polymeric material with extremely high water absorption, and since it can achieve its purpose with a very small amount of polymeric material, it can be provided at an extremely low cost. Can be done.
−■上・下対称の積層構造であるから、表裏面の区別な
く使用することができ、また表面側のフィルムが焼損し
て外観が悪くなったときには裏返して再使用することも
できるので経済的である。-Since the laminated structure is symmetrical from top to bottom, it can be used without distinction between the front and back sides, and if the film on the front side is burnt out and its appearance deteriorates, it can be turned over and reused, making it economical. It is.
■柔軟で取扱いが容易であり、且つ従来のアスベスト板
等で指摘される様な健康障害もなく安全である。また全
体として保形性が優れ適切な固さを保有しているので、
該シート上を歩行する場合の安定性にも問題はない。■It is flexible and easy to handle, and it is safe and does not pose any health hazards like those associated with conventional asbestos boards. In addition, it has excellent shape retention and appropriate hardness as a whole, so
There is no problem with stability when walking on the sheet.
■上記■〜■に示す様な特徴を有しているところから、
溶接作業におけるノロ受は等に限らず種々の高温物質が
飛散してくる恐れのある部分の防護シートや防炎幕(カ
ーテン)等として幅広く実用化することができ、更には
一時的に高温にさらされる機材・機器や人体の防護シー
トとして活用することもできる。■Since it has the characteristics shown in ■~■ above,
Slag catchers in welding work can be used in a wide range of practical applications, such as protective sheets and flameproof curtains for areas where various high-temperature substances may be scattered. It can also be used as a protective sheet for exposed equipment, equipment, and the human body.
第1図は本発明シートの基本的な構造を示す断面拡大模
式図、第2図は高温物質を受けたときの状態を説明する
ための要部拡大模式図、第3図は本発明の他の実施例を
示す一部破断斜視図である。
1・・・含水ゲル層 2・・・無機質繊維層3・
・・水分揮発防止用フィルム
sh・・・分断用シール部Fig. 1 is an enlarged cross-sectional schematic diagram showing the basic structure of the sheet of the present invention, Fig. 2 is an enlarged schematic diagram of the main part to explain the state when exposed to high-temperature substances, and Fig. 3 is a schematic enlarged cross-sectional diagram showing the basic structure of the sheet of the present invention. FIG. 2 is a partially cutaway perspective view showing an embodiment of the present invention. 1... Hydrogel layer 2... Inorganic fiber layer 3.
・・Film for preventing moisture volatilization sh ・・Seal part for separation
Claims (1)
た無機質繊維層が上記含水ゲル層と直接々触する様に積
層され、更に該積層物の両面は水分揮発防止フィルムで
被覆されると共に、該水分揮発防止フィルムの周縁がシ
ールされたものであることを特徴とする耐熱耐火シート
。A wet inorganic fiber layer is laminated on both sides of a hydrogel layer containing a superabsorbent polymeric substance so as to be in direct contact with the hydrogel layer, and both sides of the laminate are further covered with a film to prevent moisture volatilization. Additionally, a heat-resistant and fire-resistant sheet characterized in that the periphery of the moisture volatilization prevention film is sealed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14171087A JPS63306036A (en) | 1987-06-06 | 1987-06-06 | Heat-resistant refractory sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14171087A JPS63306036A (en) | 1987-06-06 | 1987-06-06 | Heat-resistant refractory sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63306036A true JPS63306036A (en) | 1988-12-14 |
Family
ID=15298400
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14171087A Pending JPS63306036A (en) | 1987-06-06 | 1987-06-06 | Heat-resistant refractory sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63306036A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017022241A1 (en) * | 2015-08-04 | 2017-02-09 | パナソニックIpマネジメント株式会社 | Insulating sheet, and seatback-equipped seat and cold weather garment employing same |
JP6355790B1 (en) * | 2017-04-03 | 2018-07-11 | 井前工業株式会社 | Fireproof insulation sheet |
CN112252628A (en) * | 2020-10-16 | 2021-01-22 | 江苏海美新材料有限公司 | Sticking process of anti-warping PVC architectural decoration film |
-
1987
- 1987-06-06 JP JP14171087A patent/JPS63306036A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017022241A1 (en) * | 2015-08-04 | 2017-02-09 | パナソニックIpマネジメント株式会社 | Insulating sheet, and seatback-equipped seat and cold weather garment employing same |
JPWO2017022241A1 (en) * | 2015-08-04 | 2018-05-24 | パナソニックIpマネジメント株式会社 | Insulation sheet, seat with backrest using the same, and winter clothes |
JP6355790B1 (en) * | 2017-04-03 | 2018-07-11 | 井前工業株式会社 | Fireproof insulation sheet |
JP2018179010A (en) * | 2017-04-03 | 2018-11-15 | 井前工業株式会社 | Fireproof heat insulation sheet |
CN112252628A (en) * | 2020-10-16 | 2021-01-22 | 江苏海美新材料有限公司 | Sticking process of anti-warping PVC architectural decoration film |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5849210A (en) | Method of preventing combustion by applying an aqueous superabsorbent polymer composition | |
US3782475A (en) | Fire extinguisher | |
EP1959883B1 (en) | Therapeutic kit employing a thermal insert | |
RU2011148325A (en) | BURNING PROTECTIVE MATERIALS | |
JPS6391237A (en) | Fabric for improved bridgewall and method of giving said fabric fire resistance | |
US4058643A (en) | Fire retardant laminates having intumescent adhesive layer comprising shellac | |
NL7909214A (en) | MULTILAYER COMPOSITE MATERIAL. | |
JPH0534921Y2 (en) | ||
JPS63306036A (en) | Heat-resistant refractory sheet | |
JP2000007416A (en) | Production of flame retardant porous product and product produced by the same | |
WO2008007158A1 (en) | Multifunction safety foil, especially fire-prevention foil | |
JP2918296B2 (en) | Self-extinguishing laminated film | |
JP4351220B2 (en) | Rugous gas rug and its manufacturing method | |
JP2024113170A (en) | Fire extinction body | |
EP1095193B1 (en) | Complex material in particular for heat insulation | |
JPS5824441A (en) | Layer structure as fireproof material and heat insulating material | |
JPS63107550A (en) | Heat-resistant refractory sheet | |
GB2028390A (en) | Fire Blanket Material | |
JP2004008564A (en) | Steam generation body | |
AU752252B2 (en) | Microwave-activated latent heat accumulator bodies | |
JPH11221872A (en) | Heat insulating fiber material | |
JP2519394Y2 (en) | Fireproof coating | |
CN220053118U (en) | Single aluminium ground emitting film | |
RU2801658C1 (en) | Fire extinguishing cloth based on basalt mesh | |
RU55605U1 (en) | FIRE PROTECTION DEVICE |