JP3101019B2 - Construction materials - Google Patents
Construction materialsInfo
- Publication number
- JP3101019B2 JP3101019B2 JP03250171A JP25017191A JP3101019B2 JP 3101019 B2 JP3101019 B2 JP 3101019B2 JP 03250171 A JP03250171 A JP 03250171A JP 25017191 A JP25017191 A JP 25017191A JP 3101019 B2 JP3101019 B2 JP 3101019B2
- Authority
- JP
- Japan
- Prior art keywords
- long metal
- component
- mat
- group
- layer
- 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 - Fee Related
Links
- 239000004035 construction material Substances 0.000 title claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 45
- 239000002184 metal Substances 0.000 claims description 45
- 239000000835 fiber Substances 0.000 claims description 40
- 239000003190 viscoelastic substance Substances 0.000 claims description 14
- 229940006076 viscoelastic substance Drugs 0.000 claims description 11
- 239000011888 foil Substances 0.000 claims description 8
- 238000010276 construction Methods 0.000 claims description 7
- 229920001296 polysiloxane Polymers 0.000 description 24
- 125000003342 alkenyl group Chemical group 0.000 description 12
- 238000001723 curing Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 10
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 239000005062 Polybutadiene Substances 0.000 description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
- 229920002857 polybutadiene Polymers 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 238000013016 damping Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 description 3
- -1 polysiloxane Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910004283 SiO 4 Inorganic materials 0.000 description 2
- 229910004738 SiO1 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical group CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 230000003139 buffering effect Effects 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000004005 microsphere Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- QRLSTWVLSWCGBT-UHFFFAOYSA-N 4-((4,6-bis(octylthio)-1,3,5-triazin-2-yl)amino)-2,6-di-tert-butylphenol Chemical compound CCCCCCCCSC1=NC(SCCCCCCCC)=NC(NC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=N1 QRLSTWVLSWCGBT-UHFFFAOYSA-N 0.000 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical group CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- 101100494773 Caenorhabditis elegans ctl-2 gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 244000256297 Euphorbia tirucalli Species 0.000 description 1
- 101100112369 Fasciola hepatica Cat-1 gene Proteins 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 101100005271 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cat-1 gene Proteins 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001336 alkenes 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
- 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
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- 229920005645 diorganopolysiloxane polymer Polymers 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Building Environments (AREA)
- Floor Finish (AREA)
- Laminated Bodies (AREA)
- Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、防振、防音、及び電磁
波遮蔽効果を備える、床板材、壁板材等の構築資材に関
するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a construction material such as a floor plate, a wall plate, etc., having a vibration-proof, sound-proof and electromagnetic wave shielding effect.
【0002】[0002]
【発明の背景】家屋の密集、団地化、高級住宅化するに
伴い、各家屋、各部屋における防振、防音対策が求めら
れるようになり、吸音、緩衝用のフエルト層やハニカム
構造層等を裏張りした高級床板材なども出廻っている。
一方、デジタル回路を応用した電子機器が急速に普及し
てきており、これらは家庭内で用いられるのは勿論、自
動車、飛行機、列車、通信設備等のありとあらゆるとこ
ろで使用されるため、いわゆる電磁波障害が問題となっ
ている。この他、各種測定機器が高精度化するにつれ
て、測定環境下における防振、電磁波遮蔽等が高い次元
で要求されるようにもなってきている。BACKGROUND OF THE INVENTION As houses become denser, more complex, and higher-grade houses, vibration and soundproofing measures are required in each house and each room, and a felt layer and a honeycomb structure layer for sound absorption and buffering are required. There are also high-grade floorboards lined with lining.
On the other hand, electronic devices to which digital circuits are applied are rapidly spreading, and these are used not only in homes but also in various places such as automobiles, airplanes, trains, and communication facilities. It has become. In addition, as various types of measuring equipment have become more accurate, vibration proofing, electromagnetic wave shielding, and the like in a measuring environment have been required at a higher level.
【0003】[0003]
【開発を試みた技術的事項】そこで、本発明は、防振、
防音、電磁波遮蔽効果ある、床板材、壁板材等の構築資
材を得ようとするものである。[Technical matters that we attempted to develop] Therefore, the present invention
An object of the present invention is to obtain building materials such as floorboards and wallboards, which have soundproofing and electromagnetic wave shielding effects.
【0004】[0004]
【目的達成の手段】即ち本出願に係る第一の発明たる構
築資材は、金属長繊維のマット状の繊維に対し、粘弾性
物質を含浸することにより、粘弾性物質の粘着性により
構築用ボードと粘接着して成ることを特徴とする。[Means of Achieving the Object] That is, the construction material according to the first invention of the present application is a viscoelastic material for matting fibers of long metal fibers.
By being impregnated with the substance, it is characterized in that it is adhered to the construction board by virtue of the tackiness of the viscoelastic substance.
【0005】また、本出願に係る第二の発明たる構築資
材は、これに加え、金属長繊維は、長尺な金属箔をコイ
ル状に巻いた円筒体の端面から旋削されたものであるこ
とを特徴とする。[0005] In addition, the construction material according to the second invention of the present application is such that, in addition to the above, the long metal fiber is obtained by turning a long metal foil from an end face of a cylindrical body wound in a coil shape. It is characterized by.
【0006】[0006]
【発明の作用】本発明の構築資材は、構築用ボードと金
属長繊維のマット状の層との積層を基本として成るた
め、金属長繊維をマット状としたものの、緩衝、防振
性、吸音、防音性、電磁波遮蔽性等が、構築資材におい
ても奏される。すなわち、構築用ボードに張り巡らされ
るように積層された金属長繊維の導電性が、電磁波を外
部へ漏洩、あるいは外部からの侵入を防ぐとともに、そ
の嵩高性と歪、変形により、防振、防音等し、さらに、
粘弾性物質を含浸して繊維を絡みついた状態とすれば、
その振動減衰性により、より高い防振効果をも発揮する
ものが得られる。また、金属長繊維に長尺な金属箔をコ
イル状に巻いた円筒体の端面から旋削されたものを用い
れば、これが容易かつ安価に製造されるため、本構築資
材も比較的安価に高性能のものが得られる。Since the construction material of the present invention is basically formed by laminating a construction board and a mat-like layer of long metal fibers, the long metal fibers are formed in a mat shape. In addition, soundproofing properties, electromagnetic wave shielding properties, and the like are also exhibited in construction materials. In other words, the conductivity of the long metal fiber laminated so as to be stretched around the construction board prevents electromagnetic waves from leaking out or entering from the outside, and its bulkiness, distortion and deformation cause vibration and sound insulation. Equal, and
By impregnating the viscoelastic substance to make the fibers entangled ,
Due to the vibration damping property, a material that also exhibits a higher vibration damping effect can be obtained. In addition, if a long metal foil wound around a long metal foil in a coil shape and turned from the end face is used, this can be easily and inexpensively manufactured. Is obtained.
【0007】[0007]
【実施例】以下、本発明を構成する要素たる金属長繊
維、粘弾性物質等について説明した後、図示実施例につ
いて説明する。先ず、金属長繊維について具体的に説明
すると、その一種としては一本の長繊維の形態であるモ
ノフィラメントがあり、またフィラメントを集束したト
ウの他、短繊維の形態のものを撚糸して長繊維としたも
のでもよく、その繊維長は数cmから数十cm程度、あ
るいはそれ以上であるのが望ましい。また、その材質
は、鉄、ステンレス、銅、黄銅、真鍮、アルミニュウ
ム、鉛等、適宜な金属を選択できるが、導電性が高く、
腐食に強いものがより望ましい。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a perspective view of a viscoelastic material according to an embodiment of the present invention. First, the metal filaments will be specifically described. As one type, there is a monofilament in the form of a single filament, and in addition to a tow in which filaments are bundled, a filament in the form of a short fiber is twisted into a filament. The fiber length is desirably about several cm to several tens cm, or more. In addition, the material can be selected from appropriate metals such as iron, stainless steel, copper, brass, brass, aluminum, and lead, but the conductivity is high,
Those that are resistant to corrosion are more desirable.
【0008】また、金属長繊維の製法としては次のよう
なものが挙げられる。すなわち、先ずその一つとして、
薄肉帯状の金属箔をロール状に巻いた円筒体の端面に横
幅のある刃先を押し当てて、この状態で円筒体を軸を中
心に回転させることで端面から金属箔を連続的に切削し
ていく方法がある。ちなみにこの方法は特開平1−15
3231号公報に詳しく記載されている方法であり、こ
の方法によれば、金属長繊維を効率よく生成し、また柔
軟性に富み、バリの少ない金属長繊維を安価に製造する
ことができる。なお、この場合の金属箔の厚さは、その
材質、硬さ等にもよるが、数μ〜数100μ、望ましく
は、数10μ程度が適当である。勿論、切削速度、送り
速度、切削幅、バイトのすくい角等の諸条件を金属箔に
合わせ調節することにより、最適な金属長繊維が得られ
る。勿論、この方法に限られる必要はなく、要は細く
て、長い、繊維状の状態で得られたものであればよく、
この他の製造方法として、溶融した金属を口金から押し
出してこれを冷却することによりモノフィラメント状の
金属長繊維として得てもよい。[0008] The following method is used as a method for producing long metal fibers. That is, first of all,
By pressing a blade with a wide width against the end face of a cylindrical body in which a thin band-shaped metal foil is rolled into a roll, the metal foil is continuously cut from the end face by rotating the cylindrical body around the axis in this state There are ways to go. Incidentally, this method is disclosed in
This method is described in detail in Japanese Unexamined Patent Publication No. 3231. According to this method, it is possible to efficiently produce long metal fibers, and to produce long metal fibers with high flexibility and less burrs at low cost. The thickness of the metal foil in this case depends on the material, hardness, etc., but is suitably several μm to several hundreds μm, preferably about several tens μm. Of course, by adjusting various conditions such as a cutting speed, a feed speed, a cutting width, and a rake angle of a cutting tool according to the metal foil, an optimum long metal fiber can be obtained. Of course, it is not necessary to be limited to this method, and it is only necessary that the method is obtained in a thin, long, fibrous state.
As another manufacturing method, a molten metal may be extruded from a die and cooled to obtain a monofilament long metal fiber.
【0009】そして、本発明では、これら金属長繊維を
マット状に絡み合わせたものを使用する。マット状の層
とするには、金属長繊維が整列されたものとして得られ
るなら、例えば、一旦これをほぐすなどした後、再度各
繊維をランダムに配置し直し、ニードルパンチして絡み
合わせる等、合成繊維における不織布製造とほぼ同様な
手法がとれる。なお、ほぐし、再配置するにあたって
は、例えば、熊手状の引っ掛け部材や、ロール間、堰の
間等を通過させる。また、マット状の層としては、厚さ
数mmから数cm程度、あるいはそれ以上とし、また、
その分散程度は、求められる構築資材としての性能、つ
まり必要とする防振、防音、電磁波遮蔽の度合いにより
定める。In the present invention, a metal long fiber entangled in a mat shape is used. In order to obtain a mat-like layer, if long metal fibers are obtained as aligned, for example, after loosening this once, each fiber is re-arranged again, needle-punched and entangled, etc. Almost the same method can be adopted as in the production of non-woven fabric using synthetic fibers. When loosening and rearranging, for example, a rake-shaped hooking member, between rolls, between weirs, or the like is passed. In addition, the thickness of the mat-like layer is about several mm to several cm, or more,
The degree of dispersion is determined by the required performance as a construction material, that is, the required degree of vibration proofing, soundproofing, and electromagnetic wave shielding.
【0010】なお、本願に言う構築用ボードとは、建築
用資材における内装材としての木質で化粧面を有する床
板材や壁板材は勿論、外装材としての木質、石膏、その
他の不燃材、合成樹脂のボード、断熱ボード等を含み、
さらにはスピーカーボックス、キャビネット等を作成す
るのに用いる工作用の資材をも含むものである。[0010] The construction board referred to in the present application is not only a wooden floorboard or a wallboard having a decorative surface as an interior material in a building material, but also a wooden material, a plaster, other non-combustible materials, a synthetic material, or an exterior material. Including resin boards, insulation boards, etc.
Further, it also includes materials for working used for making speaker boxes, cabinets and the like.
【0011】本発明では上記金属長繊維のマット状の層
を構築用ボードと積層して用いるのであるが、この金属
長繊維のマット状の層に粘弾性物質を含浸させて繊維を
絡みついた状態として用いるので、次にこの粘弾性物質
について説明する。In the present invention, the above-mentioned mat-like layer of long metal fibers is used by being laminated on a construction board. The mat-like layer of long metal fibers is impregnated with a viscoelastic substance so that the fibers are impregnated.
This viscoelastic substance will be described below because it is used as an entangled state .
【0012】まず、この粘弾性物質として好適なものに
シリコーンゲルがある。シリコーンゲルは、例えば次式
[1]で示されるシリコーンゲルの原液たるジオルガノ
ポリシロキサン(以下A成分という): RR1 2SiO−(R2 2SiO)nSiR1 2R…[1] [ただし、Rはアルケニル基であり、R1は脂肪族不飽
和結合を有しない一価の炭化水素基であり、R2は一価
の脂肪族炭化水素基(R2のうち少なくとも50モル%
はメチル基であり、アルケニル基を有する場合にはその
含有率は10モル%以下である)であり、nはこの成分
の25℃における粘度が100〜100,000cSt
になるような数である]と、25℃における粘度が50
00cSt以下であり、1分子中に少なくとも2個のS
i原子に直接結合した水素原子を有するシリコーンゲル
の原液たるオルガノハイドロジェンポリシロキサン(B
成分)とからなり、且つこのB成分中のSi原子に直接
結合している水素原子の合計量に対するA成分中に含ま
れるアルケニル基の合計量の比(モル比)が0.1〜2.
0になるように調整された混合物を硬化させることによ
り得られる付加反応型シリコーンポリマーである。First, a silicone gel suitable as the viscoelastic substance is silicone gel. Silicone gel, for example undiluted serving diorganopolysiloxane silicone gel represented by the following formula [1] (hereinafter referred to as component A): RR 1 2 SiO- (R 2 2 SiO) n SiR 1 2 R ... [1] [ Here, R is an alkenyl group, R 1 is a monovalent hydrocarbon group having no aliphatic unsaturated bond, and R 2 is a monovalent aliphatic hydrocarbon group (at least 50 mol% of R 2 ).
Is a methyl group, and when it has an alkenyl group, its content is 10 mol% or less), and n is a viscosity of the component at 25 ° C. of 100 to 100,000 cSt.
And a viscosity at 25 ° C. of 50
00 cSt or less, and at least two S
Organohydrogenpolysiloxane (B) which is a stock solution of a silicone gel having a hydrogen atom directly bonded to an i atom
Component), and the ratio (molar ratio) of the total amount of alkenyl groups contained in component A to the total amount of hydrogen atoms directly bonded to Si atoms in component B is 0.1 to 2.2.
An addition reaction type silicone polymer obtained by curing a mixture adjusted to be zero.
【0013】このシリコーンゲルについてさらに詳しく
説明すると、上記A成分は直鎖状の分子構造を有し、分
子の両末端にあるアルケニル基RがB成分中のSi原子
に直接結合した水素原子と付加して架橋構造を形成する
ことができる化合物である。この分子末端に存在するア
ルケニル基は、低級アルケニル基であることが好まし
く、反応性を考慮するとビニル基が特に好ましい。また
分子末端に存在するR1は、脂肪族不飽和結合を有しな
い一価の炭化水素基であり、このような基の具体例とし
てはメチル基、プロピル基及びヘキシル基等のようなア
ルキル基、フェニル基並びにフロロアルキル基を挙げる
ことができる。上記[1]式においてR2は一価の脂肪
族炭化水素であり、このような基の具体的な例として
は、メチル基、プロピル基及びヘキシル基等のようなア
ルキル基並びにビニル基のような低級アルケニル基を挙
げることができる。ただし、R2のうち少なくとも50
モル%はメチル基であり、R2がアルケニル基である場
合には、アルケニル基は10モル%以下の量であること
が好ましい。アルケニル基の量が10モル%を超えると
架橋密度が高くなり過ぎて高粘度になりやすい。またn
は、このA成分の25℃における粘度が通常は100〜
100,000cSt、好ましくは200〜20,000
cStの範囲内になるように設定される。The silicone gel will be described in more detail. The component A has a linear molecular structure, and alkenyl groups R at both ends of the molecule are added to hydrogen atoms directly bonded to Si atoms in the component B. Is a compound capable of forming a cross-linked structure. The alkenyl group present at the molecular terminal is preferably a lower alkenyl group, and a vinyl group is particularly preferable in consideration of reactivity. R 1 present at the molecular terminal is a monovalent hydrocarbon group having no aliphatic unsaturated bond, and specific examples of such a group include alkyl groups such as a methyl group, a propyl group, and a hexyl group. , A phenyl group and a fluoroalkyl group. In the above formula [1], R 2 is a monovalent aliphatic hydrocarbon, and specific examples of such a group include alkyl groups such as methyl group, propyl group and hexyl group, and vinyl groups. Lower alkenyl groups. Provided that at least 50 of R 2
The mol% is a methyl group, and when R 2 is an alkenyl group, the alkenyl group is preferably in an amount of 10 mol% or less. When the amount of the alkenyl group exceeds 10 mol%, the crosslinking density becomes too high and the viscosity tends to be high. And n
The viscosity of the component A at 25 ° C. is usually 100 to
100,000 cSt, preferably 200-20,000
It is set to be within the range of cSt.
【0014】上記のB成分は、A成分の架橋剤でありS
i原子に直接結合した水素原子がA成分中のアルケニル
基と付加してA成分を硬化させる。B成分は上記のよう
な作用を有していればよく、B成分としては直鎖状、分
岐した鎖状、環状、あるいは網目状などの種々の分子構
造のものが使用できる。また、B成分中のSi原子には
水素原子の他、有機基が結合しており、この有機基は通
常はメチル基のような低級アルキル基である。さらに、
B成分の25℃における粘度は通常は5000cSt以
下、好ましくは500cSt以下である。このようなB
成分の例として、分子両末端がトリオルガノシロキシ基
で封鎖されたオルガノハイドロジェンポリシロキサン、
ジオルガノシロキサンとオルガノハイドロジェンポリシ
ロキサンとの共重合体、テトラオルガノテトラハイドロ
ジェンシクロテトラシロキサン、HR1 2SiO1/2単
位とSiO 4/2単位とからなる共重合体ポリシロキサ
ン、及びHR1 2SiO 1/2単位とR1 3SiO1/2単
位とSiO 4/2単位とからなる共重合体ポリシロキサン
を挙げることができる。ただし上記式においてR1は前
記と同じ意味である。そして上記のB成分中のSiに直
接結合している水素原子の合計モル量に対するA成分中
のアルケニル基の合計モル量との比率が通常は0.1〜
2.0、好ましくは0.1〜1.0の範囲内になるように
A成分とB成分とを混合して硬化させることにより製造
される。The component B is a crosslinking agent for the component A,
The hydrogen atom directly bonded to the i atom is added to the alkenyl group in the component A to cure the component A. The B component may have any of the above-mentioned effects, and may have various molecular structures such as a linear, branched chain, cyclic, or network structure. In addition, a hydrogen atom and an organic group are bonded to the Si atom in the B component, and this organic group is usually a lower alkyl group such as a methyl group. further,
The viscosity of the component B at 25 ° C. is usually 5,000 cSt or less, preferably 500 cSt or less. Such B
Examples of the component include an organohydrogenpolysiloxane in which both molecular terminals are blocked with a triorganosiloxy group,
Copolymers of diorganosiloxane and organohydrogen polysiloxane, copolymer polysiloxane consisting of tetra organo tetra hydrogen cyclotetrasiloxane, HR 1 2 SiO1 / 2 units and SiO 4/2 units, and HR 1 2 can be mentioned copolymers polysiloxane SiO 1/2 units and R 1 3 SiO1 / 2 units and SiO 4/2 units. However, in the above formula, R 1 has the same meaning as described above. The ratio of the total molar amount of alkenyl groups in component A to the total molar amount of hydrogen atoms directly bonded to Si in component B is usually 0.1 to 0.1.
It is manufactured by mixing and curing the A component and the B component so as to be in the range of 2.0, preferably in the range of 0.1 to 1.0.
【0015】この場合の硬化反応は、通常は触媒を用い
て行なわれる。ここで使用される触媒としては、白金系
触媒が好適であり、この例としては微粉砕元素状白金、
塩化白金酸、酸化白金、白金とオレフィンとの錯塩、白
金アルコラート及び塩化白金酸とビニルシロキ酸との錯
塩を挙げることができる。このような錯塩はA成分とB
成分との合計重量に対して通常は0.1ppm(白金換
算量、以下同様)以上、好ましくは0.5ppm以上の
量で使用される。このような触媒の量の上限については
特に制限はないが、例えば触媒が液状である場合、ある
いは溶液として使用することができる場合には200p
pm以下の量で十分である。The curing reaction in this case is usually performed using a catalyst. As the catalyst used herein, a platinum-based catalyst is preferable, and examples thereof include finely pulverized elemental platinum,
Examples thereof include chloroplatinic acid, platinum oxide, complex salts of platinum and olefins, platinum alcoholates, and complex salts of chloroplatinic acid and vinyl siloxane acid. Such a complex salt is composed of A component and B component.
It is used in an amount of usually at least 0.1 ppm (amount in terms of platinum, the same applies hereinafter), preferably at least 0.5 ppm, based on the total weight of the components. The upper limit of the amount of such a catalyst is not particularly limited. For example, when the catalyst is in a liquid state or when it can be used as a solution, 200 p.
pm or less is sufficient.
【0016】そして上記のようなA成分、B成分及び触
媒を混合し、室温に放置するか、あるいは加熱すること
により硬化して本発明で使用されるシリコーンゲルが生
成する。加熱して硬化させる場合、加熱温度は通常50
〜160℃である。このようにして得られたシリコーン
ゲルは、JIS(K2207−1980、50g荷重)
で測定した針入度が通常5〜250を有する。このよう
なシリコーンゲルの硬度は、上記A成分とB成分とによ
り形成された架橋構造によって変動する。シリコーンゲ
ルの硬化前の粘度及び硬化後の針入度は、両末端がメチ
ル基であるシリコーンオイルを、得られるシリコーンゲ
ルに対して5〜75重量%の範囲内の量であらかじめ添
加することにより調整することができる。シリコーンゲ
ルは上記のようにして調整することもできるし、また市
販されているものを使用することもできる。本発明で使
用することができる市販品の例としては、CF502
7、TOUGH−3、TOUGH−4、TOUGH−
5、TOUGH−6、TOUGH−7(トーレ・ダウコ
ーニングシリコーン社製)やX32−902/cat1
300、KE1308/cat1300−L4(信越化
学工業株式会社製)、F250−121(日本ユニカ株
式会社製)等を挙げることができる。Then, the above-mentioned A component, B component and the catalyst are mixed and cured at room temperature or by heating to form the silicone gel used in the present invention. When curing by heating, the heating temperature is usually 50
160160 ° C. The silicone gel thus obtained is JIS (K2207-1980, 50 g load)
Has a penetration of usually from 5 to 250. The hardness of such a silicone gel varies depending on the crosslinked structure formed by the above-mentioned component A and component B. The viscosity before curing and the penetration after curing of the silicone gel can be determined by previously adding a silicone oil having methyl groups at both ends in an amount within the range of 5 to 75% by weight based on the obtained silicone gel. Can be adjusted. The silicone gel can be adjusted as described above, or a commercially available silicone gel can be used. Examples of commercially available products that can be used in the present invention include CF502
7, TOUGH-3, TOUGH-4, TOUGH-
5, TOUGH-6, TOUGH-7 (manufactured by Toray Dow Corning Silicone) or X32-902 / cat1
300, KE1308 / cat1300-L4 (manufactured by Shin-Etsu Chemical Co., Ltd.), F250-121 (manufactured by Nippon Yunika Co., Ltd.) and the like.
【0017】また、上記のA成分、B成分及び触媒の他
に、顔料、硬化遅延剤、難燃剤、充填剤等をシリコーン
ゲルの特性を損なわない範囲内で配合することもでき、
さらに、防振、緩衝性等を高める為に、微小中空球体の
フィラーを混入してなるシリコーンゲルを用いてもよ
く、このようなフィラー材料に日本フィライト株式会社
製造のフィライト(登録商標)や同社販売のエクスパン
セル(登録商標)、マツモトマイクロスフェアー(松本
油脂製薬株式会社製造販売)等が例示できる。Further, in addition to the above-mentioned components A, B and the catalyst, a pigment, a curing retarder, a flame retardant, a filler and the like can be blended within a range that does not impair the properties of the silicone gel.
Furthermore, in order to enhance vibration proofing, cushioning, etc., a silicone gel mixed with a fine hollow sphere filler may be used. For such a filler material, Philite (registered trademark) manufactured by Nippon Philite Co., Ltd. Examples include Expancel (registered trademark) and Matsumoto Microsphere (manufactured and sold by Matsumoto Yushi Seiyaku Co., Ltd.).
【0018】また、導電性を有するフィラーを混入して
もよく、これにはカーボンブラック、カーボンファイバ
ー、グラファイト、金属粉末、金属酸化物、金属フレー
ク、金属繊維等、そのものが導電物質の他、絶縁性の有
機、無機の微粒子にニッケル、コバルト、金、銀等の導
電物質をメッキ、コート等したものがある。このような
導電性フィラーを混入してなるシリコーンゲルを、金属
長繊維のマット状の層に含浸させて硬化させれば、電磁
波遮蔽効果は格段に向上する。In addition, a filler having conductivity may be mixed therein, such as carbon black, carbon fiber, graphite, metal powder, metal oxide, metal flake, metal fiber, etc. Organic and inorganic fine particles are plated or coated with a conductive substance such as nickel, cobalt, gold, or silver. If a silicone gel containing such a conductive filler is impregnated into a mat-like layer of long metal fibers and cured, the electromagnetic wave shielding effect is significantly improved.
【0019】上記シリコーンゲルの他、粘弾性物質とし
て好適なものにポリブタジエンゲルがある。この具体例
としては、出光アーコ株式会社製造販売のPoly b
dR−45HTがある。これは、分子末端に反応性の高
い水酸基を備えたポリブタジエンタイプの液状ポリマー
で、通常のポリウレタンと同様にイソシアネート類によ
り容易に硬化して良好な粘弾性体となるものである。そ
して、このポリブタジエンゲルは、主鎖が炭化水素のみ
からなるため、優れた耐水性、耐薬品性、電気特性をも
備え、しかも骨格が1,4結合のため、良好な低温特性
も備えている。また、液状のため加工が容易で、連続化
が行ない易い利点もある。そして、適宜の各種配合剤を
加え一次混合した後、硬化剤を加え二次混合して、含
浸、シート成形等して用いることとなる。In addition to the above-mentioned silicone gel, a polybutadiene gel is also suitable as a viscoelastic substance. As a specific example, Poly b manufactured and sold by Idemitsu Arco Co., Ltd.
There is dR-45HT. This is a polybutadiene-type liquid polymer having a highly reactive hydroxyl group at the molecular end, and is easily cured by isocyanates to form a good viscoelastic body like ordinary polyurethane. The polybutadiene gel has excellent water resistance, chemical resistance, and electrical properties because the main chain is composed of only hydrocarbons, and also has good low-temperature properties because the skeleton has 1,4 bonds. . In addition, there is an advantage that processing is easy because of the liquid state, and continuity can be easily performed. Then, after appropriately adding various compounding agents and performing primary mixing, a curing agent is added and secondary mixing is performed, and impregnation, sheet molding and the like are used.
【0020】なお、配合剤には、強度、硬さ、耐熱性の
ための充填剤としてカーボンブラック、シリカ、アルミ
ナ、炭酸カルシウムがあり、粘度調整の伸展剤としてプ
ロセスオイル、アスファルトがあり、硬化速度の調整の
ための触媒としてジブチル錫ジラウレートがあり、耐熱
性向上、酸化防止剤としてチバガイギ株式会社製のイル
ガノックス565、大内新興化学株式会社製のノックラ
ックNS−6、耐オゾン性のための紫外線吸収剤として
チバガイギ株式会社製のチヌビン327があり、難燃化
剤として水酸化アルミニウム、ホウ砂、塩素化パラフィ
ン、酸化アンチモンがあり、また、硬化剤としてはリレ
ンジイソシアネート、メチレンジイソシアネートがあ
る。その他、前記フィラー類も勿論混入させることがで
きる。The compounding agents include carbon black, silica, alumina and calcium carbonate as fillers for strength, hardness and heat resistance, and process oil and asphalt as extenders for adjusting viscosity. There is dibutyltin dilaurate as a catalyst for adjusting the temperature, and as a heat resistance improving and antioxidant, Irganox 565 manufactured by Ciba Geigy Co., Ltd., Knocklac NS-6 manufactured by Ouchi Shinko Chemical Co., Ltd. As an ultraviolet absorber, there is Tinuvin 327 manufactured by Ciba Geigy Co., Ltd., as a flame retardant, there are aluminum hydroxide, borax, chlorinated paraffin, and antimony oxide. As a curing agent, there is lylene diisocyanate or methylene diisocyanate. In addition, the fillers can of course be mixed.
【0021】そして、例えば、好適な例として、上記R
−45HTの100部、消泡剤としての信越シリコーン
株式会社製のTAS750を0.005部、触媒として
の共同薬品株式会社製のDBTDL KS−1260を
0.005部、硬化剤として日本ポリウレタン工業株式
会社製のMillionate MR−200(NCO
の含有率30.9重量%)を8.3部、さらに微少中空
球体として松本油脂製薬株式会社製のマイクロスフェア
ーF−80EDを1部用い、先ず、これらの内硬化剤を
除いた成分を室温で十分に撹拌混合し、次いでこれに硬
化剤を加え、さらに撹拌混合の上均一な液状物を得て、
減圧下にて脱泡した後、金属長繊維のマット状の層の上
に硬化前の液状物を流し出し、その後、これらを上下の
ロール間に通しつつ加熱トンネルを通過させて加熱硬化
させ、ポリブタジエンゲルを含浸させた金属長繊維のシ
ートを得ることができる。なお、このようにして得たポ
リブタジエンゲルを含浸させた金属長繊維のシートは、
前記シリコーンゲルに近い緩衝性を有し、シリコーンゲ
ルよりも比較的安価なため、本発明構築資材に好適に用
いられる。For example, as a preferred example, the above R
100 parts of -45HT, 0.005 part of TAS750 manufactured by Shin-Etsu Silicone Co., Ltd. as an antifoaming agent, 0.005 part of DBTDL KS-1260 manufactured by Kyodo Yakuhin as a catalyst, and Nippon Polyurethane Industry Co., Ltd. as a curing agent Company made Millionate MR-200 (NCO
8.3 parts), and 1 part of Microsphere F-80ED manufactured by Matsumoto Yushi Seiyaku Co., Ltd. as micro hollow spheres. Stir and mix well at room temperature, then add the curing agent, and further stir and mix to obtain a uniform liquid,
After defoaming under reduced pressure , on the mat-like layer of long metal fibers
Pour out the liquid material before curing, and then
Heat curing by passing through a heating tunnel while passing between rolls
Thus, a sheet of long metal fibers impregnated with polybutadiene gel can be obtained. The sheet of long metal fiber impregnated with the polybutadiene gel thus obtained is
Since it has a buffering property close to that of the silicone gel and is relatively inexpensive than the silicone gel, it is suitably used for the construction material of the present invention.
【0022】次に、本発明構築資材を図示実施例につい
て説明する。図1は、構築資材の一例の縦断面を示すも
ので、この例では構築用ボードとしてのいわゆる化粧ベ
ニヤ板に、金属長繊維のマット状の層を積層している。
すなわち、1が化粧ベニヤ板で、11が化粧面、その裏
面12に金属長繊維のマット状の層2が接着され一体と
なっている。図2は他の構築資材の一例を示すもので、
この例では金属長繊維のマット状の層2の上下各々にベ
ニヤ板1、3を接着したものとなっており、その一方の
ベニヤ板1は化粧面11を有し、他方のベニヤ板3はこ
れより薄く、化粧面を有しないものとしてある。図3
は、本願実施例の縦断面であり、粘弾性物質の層を積層
したもので、この例では前記ポリブタジエンゲルを含浸
させた金属長繊維のシートマット状の層4として、これ
を化粧ベニヤ板1に積層している。Next, the construction material of the present invention will be described with reference to the illustrated embodiment. FIG. 1 shows a longitudinal section of an example of a construction material. In this example, a mat-like layer of long metal fibers is laminated on a so-called decorative plywood as a construction board.
That is, 1 is a decorative plywood plate, 11 is a decorative surface, and a mat-shaped layer 2 of a long metal fiber is adhered to a back surface 12 thereof to be integrated. FIG. 2 shows an example of another construction material.
In this example, veneer plates 1 and 3 are bonded to the upper and lower surfaces of a mat-like layer 2 of long metal fibers, one of which has a decorative surface 11 and the other is 3 thinner. It does not have a cosmetic surface. FIG.
Is a longitudinal section of the embodiment of the present application, in which a layer of a viscoelastic substance is laminated, and in this example, as a sheet mat-shaped layer 4 of a long metal fiber impregnated with the polybutadiene gel, this is used for the decorative veneer board 1. Laminated.
【0023】なお、金属長繊維のマット状の層にポリブ
タジエンゲルやシリコーンゲル等の粘弾性物質を含浸さ
せるに当っては、金属長繊維のマット状の層の上にこれ
らの硬化前の原液を流し出し、その後、これらを上下の
ロール間に通しつつ加熱トンネルを通過させて硬化させ
る等の手法が採れる。また、各層を接着するにあたって
は、粘弾性物質の粘着性により粘接着させる。また、上
記実施例では金属長繊維のマット状の層は全体が均一な
厚さを有する平坦な層を前提としたが、本発明はこれに
限らず、マット状の層が適宜なパターンにて凹凸、いわ
ゆるエンボスが付けられたものであってもよいこと勿論
である。また、全体を適宜な大きさ、例えば、30cm
×30cm等のタイル状ものとし、これを相互に嵌め合
わせて使うようにしたり、裏面一部には、床等の骨木に
固着するため、金属長繊維のマット状の層を積層しない
部分があってもよい。In impregnating the mat-like layer of long metal fibers with a viscoelastic substance such as polybutadiene gel or silicone gel, the uncured stock solution is placed on the mat-like layer of long metal fibers. After that, it is possible to employ a technique of hardening by flowing through a heating tunnel while passing between the upper and lower rolls. In bonding the layers, the layers are viscously adhered by the tackiness of the viscoelastic substance. Further, in the above embodiment, the mat-shaped layer of the long metal fiber is assumed to be a flat layer having a uniform thickness as a whole, but the present invention is not limited to this, and the mat-shaped layer is formed by an appropriate pattern. It is a matter of course that the surface may be provided with irregularities, so-called emboss. In addition, the whole is appropriately sized, for example, 30 cm.
It is a tile shape of × 30 cm etc., and it is used by fitting it to each other, and on the back part, there is a part where a mat-like layer of long metal fiber is not laminated to fix it to the bone tree such as the floor. There may be.
【0024】[0024]
【発明の効果】このような本発明構築資材を、制御室、
コンピュータ室を始め、広く居間、勉強部屋等を構成す
る板材、さらにはスピーカーボックスやキャビネット等
を作成する板材として用いれば、金属長繊維のマット状
の繊維とそれに含浸した粘弾性物質により、防振、防
音、電磁波遮蔽効果が発揮され、振動、騒音問題や電磁
波障害を心配する必要がなくなる。The construction material of the present invention is supplied to a control room,
If it is used as a plate material for computer rooms, living rooms, study rooms, etc., as well as for speaker boxes and cabinets, vibration-damping is achieved by mat-like fibers of metal long fibers and viscoelastic materials impregnated in them. In addition, soundproofing and electromagnetic wave shielding effects are exhibited, and there is no need to worry about vibration, noise problems and electromagnetic wave interference.
【図1】本発明の構築資材を説明するための構築資材の
一例を示す縦断面図である。FIG. 1 is a longitudinal sectional view showing an example of a construction material for explaining a construction material of the present invention.
【図2】本発明の構築資材を説明するための他の構築資
材の一例を示す縦断面図である。FIG. 2 is a longitudinal sectional view showing an example of another construction material for explaining the construction material of the present invention .
【図3】本発明構築資材の一実施例の縦断面図である。FIG. 3 is a longitudinal sectional view of one embodiment of the construction material of the present invention.
1 化粧ベニヤ板 11 化粧面 2 金属長繊維のマット状の層 3 ベニヤ板 4 ポリブタジエンゲルを含浸させた金属長繊維のシ
ートマット状の層DESCRIPTION OF SYMBOLS 1 Decorative veneer board 11 Decorative face 2 Matt-like layer of long metal fiber 3 Veneer board 4 Sheet mat-like layer of long metal fiber impregnated with polybutadiene gel
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI H05K 9/00 H05K 9/00 W (58)調査した分野(Int.Cl.7,DB名) E04B 1/92 B32B 7/02 B32B 15/02 E04F 15/18 H05K 9/00 ────────────────────────────────────────────────── ─── Continued on the front page (51) Int.Cl. 7 identification code FI H05K 9/00 H05K 9/00 W (58) Fields investigated (Int. Cl. 7 , DB name) E04B 1/92 B32B 7 / 02 B32B 15/02 E04F 15/18 H05K 9/00
Claims (2)
弾性物質を含浸することにより、粘弾性物質の粘着性に
より構築用ボードと粘接着して成ることを特徴とする構
築資材。1. A construction material characterized in that mat-like fibers of long metal fibers are impregnated with a viscoelastic substance and are adhered to a construction board by virtue of the tackiness of the viscoelastic substance.
ル状に巻いた円筒体の端面から旋削されたものであるこ
とを特徴とする請求項1記載の構築資材。2. The construction material according to claim 1, wherein the long metal fiber is turned from an end face of a cylindrical body in which a long metal foil is wound in a coil shape.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP03250171A JP3101019B2 (en) | 1991-06-26 | 1991-06-26 | Construction materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP03250171A JP3101019B2 (en) | 1991-06-26 | 1991-06-26 | Construction materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH055332A JPH055332A (en) | 1993-01-14 |
| JP3101019B2 true JP3101019B2 (en) | 2000-10-23 |
Family
ID=17203879
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP03250171A Expired - Fee Related JP3101019B2 (en) | 1991-06-26 | 1991-06-26 | Construction materials |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3101019B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4733952B2 (en) | 2004-09-24 | 2011-07-27 | 株式会社マキタ | Cutting machine |
-
1991
- 1991-06-26 JP JP03250171A patent/JP3101019B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH055332A (en) | 1993-01-14 |
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