JPH0830310B2 - Cushioning heavy walking floor material - Google Patents
Cushioning heavy walking floor materialInfo
- Publication number
- JPH0830310B2 JPH0830310B2 JP2107673A JP10767390A JPH0830310B2 JP H0830310 B2 JPH0830310 B2 JP H0830310B2 JP 2107673 A JP2107673 A JP 2107673A JP 10767390 A JP10767390 A JP 10767390A JP H0830310 B2 JPH0830310 B2 JP H0830310B2
- Authority
- JP
- Japan
- Prior art keywords
- synthetic resin
- layer
- thermoplastic synthetic
- floor material
- cushioning
- 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
- 239000000463 material Substances 0.000 title claims description 63
- 229920003002 synthetic resin Polymers 0.000 claims description 68
- 239000000057 synthetic resin Substances 0.000 claims description 68
- 229920001169 thermoplastic Polymers 0.000 claims description 54
- 239000004416 thermosoftening plastic Substances 0.000 claims description 54
- 239000006260 foam Substances 0.000 claims description 29
- 238000010438 heat treatment Methods 0.000 claims description 28
- 238000005187 foaming Methods 0.000 claims description 11
- 239000010410 layer Substances 0.000 description 73
- 229920005989 resin Polymers 0.000 description 26
- 239000011347 resin Substances 0.000 description 26
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 20
- 239000000203 mixture Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 10
- 239000000835 fiber Substances 0.000 description 8
- 239000003381 stabilizer Substances 0.000 description 8
- 238000009408 flooring Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000007789 gas Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000004745 nonwoven fabric Substances 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000007639 printing Methods 0.000 description 5
- 239000002216 antistatic agent Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 239000003365 glass fiber Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000003373 anti-fouling effect Effects 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 238000010022 rotary screen printing Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- SPWVOTAHZLTQIV-UHFFFAOYSA-N 2,2,2-tributoxyethyl dihydrogen phosphite Chemical compound CCCCOC(COP(O)O)(OCCCC)OCCCC SPWVOTAHZLTQIV-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 241000047703 Nonion Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000008258 liquid foam Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229920006352 transparent thermoplastic Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
- Floor Finish (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、強度および歩行性に優れ、かつ反りや収縮
の抑制されたクッション性重歩行床材に関する。TECHNICAL FIELD The present invention relates to a cushioned heavy walking floor material which is excellent in strength and walkability and in which warpage and contraction are suppressed.
従来の床材としては、例えば基材層の表面に熱可塑性
合成樹脂層を積層してなるいわゆるソリッド層のみから
なる床材あるいは基材層の表面に着色合成樹脂粒を散布
したのち加熱圧縮して形成される着色合成樹脂シートか
らなる床材などが広く使用されているが、これらの床材
は、床面に硬い感じが残り、歩行性が悪いという理由か
ら、少なくとも基材層の表面に熱可塑性合成樹脂層が積
層され、かつ該基材層の裏面には化学発泡により形成さ
れた熱可塑性合成樹脂発泡層が積層されてなるクッショ
ン性重歩行床材が提唱されている。As a conventional flooring material, for example, a flooring material consisting of a so-called solid layer formed by laminating a thermoplastic synthetic resin layer on the surface of a base material layer or a surface of a base material layer is sprayed with colored synthetic resin particles and then heated and compressed. Floor materials made of colored synthetic resin sheets are widely used.However, these floor materials leave a hard feeling on the floor surface and have poor walkability, so at least on the surface of the base material layer. A cushioning heavy walking floor material has been proposed in which a thermoplastic synthetic resin layer is laminated and a thermoplastic synthetic resin foam layer formed by chemical foaming is laminated on the back surface of the base material layer.
しかしながら、このような基材層の裏面に化学発泡に
より形成された熱可塑性合成樹脂発泡層を積層した床材
では、所望の歩行性(クッション性)は得られるもの
の、床材の上を多数の人々が歩行した場合などの外的負
荷に対して充分な強度が得られず、従って経時的に床材
の表面磨耗、へたりなどが生じ、床材としての商品価値
を著しく低下させるという問題点を有している。However, although a desired walkability (cushioning property) can be obtained with a floor material in which a thermoplastic synthetic resin foam layer formed by chemical foaming is laminated on the back surface of such a base material layer, many Sufficient strength cannot be obtained against external loads such as when people walk, so the surface of the flooring material may wear down and settle down over time, significantly reducing the commercial value of the flooring material. have.
本発明は、このような従来技術を背景になされたもの
で、外的負荷に対して優れた強度を有するとともに歩行
性にも優れ、さらには反りや収縮も抑制されたクッショ
ン性重歩行床材を提供することを目的とする。The present invention has been made on the basis of such a conventional technique, and has a cushioning type heavy walking floor material which has excellent strength against external load and also has excellent walking property, and further, warpage and contraction are suppressed. The purpose is to provide.
本発明は、少なくとも基材層の表面に熱可塑性合成樹
脂層が積層され、かつ該基材層の裏面には機械発泡によ
り形成された熱可塑性合成樹脂発泡層が積層された積層
構造体からなり、該積層構造体を該熱可塑性合成樹脂発
泡層が溶融しない加熱条件下で加熱してなるクッション
性重歩行床材を提供するものである。The present invention comprises a laminated structure in which a thermoplastic synthetic resin layer is laminated on at least the surface of a base material layer, and a thermoplastic synthetic resin foam layer formed by mechanical foaming is laminated on the back surface of the base material layer. The present invention provides a cushioning heavy walking floor material obtained by heating the laminated structure under a heating condition in which the thermoplastic synthetic resin foam layer does not melt.
以下、図面に基づき本発明を詳細に説明する 第1図は、本発明のクッション性重歩行床材の一例を
示したものであり、クッション性重歩行床材Aは、少な
くとも基材層10の表面に熱可塑性合成樹脂層20が積層さ
れ、かつ該基材層10の裏面には機械発泡により形成され
た熱可塑性合成樹脂発泡層30が積層されてなるものであ
る。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail with reference to the drawings. FIG. 1 shows an example of the cushioning heavy walking floor material of the present invention. A thermoplastic synthetic resin layer 20 is laminated on the front surface, and a thermoplastic synthetic resin foam layer 30 formed by mechanical foaming is laminated on the rear surface of the base material layer 10.
本発明に使用する基材層10としては、フェルト状シー
ト、織布、編布、不織布などの寸法安定性に優れたもの
であれば単層のものでも2層以上の複層のものでも使用
できるが、特に寸法安定性の面からアスベストシート、
アスベスト、ガラス繊維、炭素繊維、パルプ、ポリエス
テル繊維などの無機および/または有機繊維の少なくと
も2種以上を混合したシート、ガラス繊維紙、紙などが
好ましい。The base material layer 10 used in the present invention may be a single layer or a multi-layered material having two or more layers, as long as it has excellent dimensional stability such as felt-like sheet, woven fabric, knitted fabric and non-woven fabric. Yes, but especially from the aspect of dimensional stability, asbestos sheet,
A sheet in which at least two kinds of inorganic and / or organic fibers such as asbestos, glass fiber, carbon fiber, pulp and polyester fiber are mixed, glass fiber paper, paper and the like are preferable.
また、ガラス繊維、炭素繊維、合成繊維などからなる
織物と不織布の積層体なども使用できる。Further, a laminated body of a woven fabric and a non-woven fabric made of glass fiber, carbon fiber, synthetic fiber or the like can also be used.
さらに、必要に応じ、これらの基材層10に、導電性物
質、例えばカーボン粉末、カーボン短繊維、表面導電化
処理した無機および有機の粉末または短繊維〔導電性炭
酸カルシウムT130−2500(日東粉化(株)製)、EC−
1、EC−5(いずれも丸尾カルシュウム(株)製)、デ
ントールWK−100S(大塚化学(株)製)、サンダーロン
SS−N(日本蚕毛染色(株)製)〕などを含む導電性樹
脂液を含浸処理したものや、そのほか抄紙法により不織
布やガラス混抄紙などその紙を製造する際に、導電性繊
維、導電性粉末、導電処理された粉末や繊維などを混抄
したものや、これらの導電性繊維や導電処理された繊維
を織り込んだり編みこんだりした織布、編布などが使用
できる。Furthermore, if necessary, in these base material layers 10, a conductive substance such as carbon powder, carbon short fibers, surface-conductive inorganic and organic powders or short fibers (conductive calcium carbonate T130-2500 (Nitto Powder Chemical Co., Ltd., EC-
1, EC-5 (both manufactured by Maruo calcium Co., Ltd.), Dentor WK-100S (manufactured by Otsuka Chemical Co., Ltd.), Thunderon
When the paper is manufactured by impregnating a conductive resin solution containing SS-N (manufactured by Japan Silkworm Dyeing Co., Ltd.), etc., or other non-woven fabrics, glass-blended papers, etc. A conductive powder, a mixture of conductively-treated powder and fibers, and a woven or knitted fabric in which these conductive fibers and conductively-treated fibers are woven or knitted can be used.
なお、この基材層10の厚みは、通常、0.1〜2mmが好ま
しく、厚みが0.1mm未満の場合には得られる床材の強度
が弱くなり、一方2mmを超えるとコスト高になる。The thickness of the base material layer 10 is usually preferably 0.1 to 2 mm, and if the thickness is less than 0.1 mm, the strength of the floor material obtained will be weak, while if it exceeds 2 mm, the cost will be high.
本発明の熱可塑性合成樹脂層20を構成する主成分の熱
可塑性合成樹脂としては、例えば塩化ビニル系樹脂、ア
クリル樹脂、酢酸ビニル樹脂、ポリエチレン、ポリプロ
ピレン、エチレン−酢酸ビニル共重合樹脂、ウレタン樹
脂などが挙げられるが、耐磨耗性やコスト面から考慮し
て塩化ビニル系樹脂が好ましい。Examples of the main component of the thermoplastic synthetic resin that constitutes the thermoplastic synthetic resin layer 20 of the present invention include vinyl chloride resin, acrylic resin, vinyl acetate resin, polyethylene, polypropylene, ethylene-vinyl acetate copolymer resin, urethane resin and the like. However, vinyl chloride resins are preferable in consideration of abrasion resistance and cost.
本発明における塩化ビニル系樹脂とは、ポリ塩化ビニ
ル樹脂および塩化ビニルと他のモノマー、例えばエチレ
ン、酢酸ビニル、ビニルエーテル、マレイン酸エステ
ル、(メタ)アクリル酸、(メタ)アクリル酸エステ
ル、アクリロニトリル、ウレタンなどとの共重合体や、
そのほかポリ塩化ビニル樹脂と、他のポリマーとの混合
物も含むものである。The vinyl chloride resin in the present invention means polyvinyl chloride resin and vinyl chloride and other monomers such as ethylene, vinyl acetate, vinyl ether, maleic acid ester, (meth) acrylic acid, (meth) acrylic acid ester, acrylonitrile and urethane. A copolymer with
In addition, it also includes a mixture of a polyvinyl chloride resin and another polymer.
また、熱可塑性合成樹脂層20の厚みは、0.1〜5.0mmが
好ましく、0.1mm未満のものでは人の歩行などにより熱
可塑性合成樹脂層が短時間に磨耗してしまって床材の寿
命が短くなり、一方5.0mmを超えると床材自体が硬くな
り施工に不便であるとともに、反りや収縮が発生し易く
なる。Further, the thickness of the thermoplastic synthetic resin layer 20 is preferably 0.1 to 5.0 mm, and if the thickness is less than 0.1 mm, the thermoplastic synthetic resin layer is abraded in a short time due to walking of a person and the life of the floor material is shortened. On the other hand, if it exceeds 5.0 mm, the floor material itself becomes hard, which is inconvenient for construction, and warpage and shrinkage easily occur.
さらに、熱可塑性合成樹脂層20は、単層でも複層でも
よく、複層にする場合は、例えば、熱可塑性合成樹脂層
20を最上層の上引層20aとその下部に配置する中間層20b
とで構成させ、上引層20aと中間層20bとの間に印刷層20
cを介在させてもよい。Further, the thermoplastic synthetic resin layer 20 may be a single layer or multiple layers, and in the case of forming multiple layers, for example, the thermoplastic synthetic resin layer
The upper layer 20a is the uppermost layer 20a and the intermediate layer 20b is disposed below the upper layer 20a.
And the printing layer 20 between the upper coating layer 20a and the intermediate layer 20b.
You may interpose c.
さらに、この場合、上引層20aは、透明または半透明
にした方が中間層20b、印刷層20cを有色にした場合に、
より効果的に意匠効果を出すことができる。また、この
上引層20aの厚みは、0.05〜1mmが好ましい。これは、厚
みが0.05mm未満ものでは耐磨耗性に乏しく、一方1mmを
超えると床材が表面側に反りやすく、また価格も高くな
るためである。Furthermore, in this case, the upper coating layer 20a, when the transparent or semi-transparent one is the intermediate layer 20b and the printing layer 20c is colored,
The design effect can be produced more effectively. Further, the thickness of the overcoat layer 20a is preferably 0.05 to 1 mm. This is because if the thickness is less than 0.05 mm, the abrasion resistance is poor, while if it exceeds 1 mm, the floor material tends to warp to the surface side and the price becomes high.
また、この表面層は、着色合成樹脂製チップを使用す
ることにより意匠性を向上させた床材とすることもでき
る。In addition, this surface layer can also be used as a floor material whose design is improved by using colored synthetic resin chips.
さらに、熱可塑性合成樹脂層20の表面にロータリース
クリーン印刷法などにより塩化ビニル樹脂ペーストなど
を厚盛り印刷して意匠性を向上させることもできるし、
エンボス法により凹凸を形成することもできる(エンボ
スは、機械発泡による熱可塑性合成樹脂発泡層を形成す
る前に実施してもよいし、形成したのちに実施してもよ
い)。Further, it is also possible to thickly print a vinyl chloride resin paste or the like on the surface of the thermoplastic synthetic resin layer 20 by a rotary screen printing method or the like to improve the design.
It is also possible to form irregularities by an embossing method (embossing may be carried out before forming the thermoplastic synthetic resin foam layer by mechanical foaming or after forming it).
さらにまた、熱可塑性合成樹脂層表面(厚盛り印刷を
した場合にはこれも含む)に汚れ防止を目的として、ア
クリル系防汚塗料などの防汚塗料を塗布してもよい。Furthermore, an antifouling paint such as an acrylic antifouling paint may be applied to the surface of the thermoplastic synthetic resin layer (including this when thick printing is performed) for the purpose of preventing stains.
さらにまた、熱可塑性合成樹脂層20は、必要に応じ、
帯電防止性可塑剤および/または帯電防止剤を混入して
形成させることもできる。Furthermore, the thermoplastic synthetic resin layer 20, if necessary,
It can also be formed by incorporating an antistatic plasticizer and / or an antistatic agent.
熱可塑性合成樹脂層20内に混入される帯電防止性可塑
剤としては、トリブトキシエチルホスフュート(大八化
学(株)製、TBXP)、ブチルジグリコールアジペート
(大八化学(株)製、BXA)、サンソサイザーC−1100
(新日本理化学(株)製)、HA−100、AM−801、AM−80
1Aいずれも積水化学(株)製)などが好ましく、目的に
応じてジオクチルフタレート、ジブチルフタレート、ブ
チルベンジルフタレート、ジオクチルアジペート、ジヘ
キシルフタレート、ジイソノニルフタレートなどの汎用
の可塑剤を一部あるいは全部を置換して使用され、また
この配合量は、合成樹脂100重量部に対して通常、5〜1
00重量部が好ましい。As the antistatic plasticizer mixed in the thermoplastic synthetic resin layer 20, tributoxyethyl phosphite (manufactured by Daihachi Chemical Co., Ltd., TBXP), butyldiglycol adipate (manufactured by Daihachi Chemical Co., Ltd., BXA), Sansosizer C-1100
(Manufactured by Shin Nihon Rikagaku Co., Ltd.), HA-100, AM-801, AM-80
1A are all manufactured by Sekisui Chemical Co., Ltd., etc., and some or all of general-purpose plasticizers such as dioctyl phthalate, dibutyl phthalate, butylbenzyl phthalate, dioctyl adipate, dihexyl phthalate, and diisononyl phthalate are substituted according to the purpose. The compounding amount is usually 5 to 1 with respect to 100 parts by weight of the synthetic resin.
00 parts by weight is preferred.
また、熱可塑性合成樹脂層20内に混入される帯電防止
剤としては、カチオン系、アニオン系、ノニオン系など
の通常使用される帯電防止剤が挙げられ、その配合量
は、通常、熱可塑性合成樹脂100重量部に対して、0.2〜
10重量部が好ましい。以上の配合剤は、単独で使用して
も2種類以上を混合して使用してもよい。Examples of the antistatic agent mixed in the thermoplastic synthetic resin layer 20 include cation-based, anion-based, nonion-based and other commonly used antistatic agents, and the amount thereof is usually thermoplastic synthetic. 0.2 to 100 parts by weight of resin
10 parts by weight is preferred. The above compounding agents may be used alone or in combination of two or more.
そのほか、熱可塑性合成樹脂層20には、必要に応じ
て、その他の可塑剤、安定剤、充填剤、粘度調整剤、発
泡剤、防黴剤、着色剤などの配合剤を添加することが可
能である。In addition, other compounding agents such as plasticizers, stabilizers, fillers, viscosity modifiers, foaming agents, mildew-proofing agents, and colorants can be added to the thermoplastic synthetic resin layer 20 if necessary. Is.
熱可塑性合成樹脂層20を単層で形成する場合には、基
材上に塩化ビニル樹脂粒子などのような熱可塑性合成樹
脂製粒子を布設して、これを加熱溶融または軟化させて
フラットエンボスローラにより加圧焼結させて形成する
ことができる。When the thermoplastic synthetic resin layer 20 is formed as a single layer, particles of thermoplastic synthetic resin such as vinyl chloride resin particles are laid on a base material, and heated and melted or softened to flatten the emboss roller. Can be formed by pressure sintering.
熱可塑性合成樹脂粒子としては、着色合成樹脂粒本体
表面に透明熱可塑性合成樹脂層を形成させたものや、複
数の着色合成樹脂が入り乱れた流れ模様を有する着色合
成樹脂粒子や、着色合成樹脂粒本体表面にカーボンブラ
ックを含有する導電性熱可塑性合成樹脂層を形成させた
ものなど、一般に使用されるものであればいずれのもの
も使用できる。As the thermoplastic synthetic resin particles, those having a transparent thermoplastic synthetic resin layer formed on the surface of the colored synthetic resin particles main body, colored synthetic resin particles having a disordered flow pattern containing a plurality of colored synthetic resins, and colored synthetic resin particles Any generally used one can be used, such as one having a conductive thermoplastic synthetic resin layer containing carbon black formed on the surface of the main body.
また、基材上に熱可塑性合成樹脂細片を配列し、各熱
可塑性合成樹脂細片間にマトリックス樹脂粉末もしくは
溶液を充填し、加熱焼結もしくはゲル化させたものなど
が使用できる。Further, it is possible to use a material in which thermoplastic synthetic resin strips are arranged on a base material, matrix resin powder or solution is filled between the thermoplastic synthetic resin strips, and heat-sintered or gelled.
熱可塑性合成樹脂発泡層30を構成する主成分の熱可塑
性合成樹脂としては、熱可塑性合成樹脂層20の場合と同
様のものが使用でき、発泡層を形成させるための手段と
しては、塩化ビニル樹脂ペーストなどに整泡剤を添加
し、これに機械的に気体(空気、ガスなど)を混入する
手段や、塩化ビニル樹脂ペーストに高圧でガスを溶かし
込み、該ガスを常圧で膨張させる手段などを採用するこ
とができ、またガスとしては、炭酸ガス、窒素ガスなど
の不活性ガスが使用できる。As the thermoplastic synthetic resin as the main component constituting the thermoplastic synthetic resin foam layer 30, the same one as in the case of the thermoplastic synthetic resin layer 20 can be used, and as a means for forming the foam layer, a vinyl chloride resin is used. Means for mechanically mixing gas (air, gas, etc.) with a foam stabilizer added to the paste, etc., means for dissolving gas at high pressure in vinyl chloride resin paste, and expanding this gas at normal pressure In addition, an inert gas such as carbon dioxide gas or nitrogen gas can be used as the gas.
整泡剤としては、一般に使用されているものであれば
何でも使用することができ、例えばメチルシロキサンエ
マルジョン、メチルシロキサン、キシレン溶液などのシ
リコン系整泡剤、フッ素系整泡剤、脂肪酸縮合物、アル
キルアリルスルホネート系、オレイン酸セリシノール酸
の金属石鹸、グアニジン塩類、第四級アンモニウム化合
物、アルデヒド−アミンの縮合生成物などが使用でき
る。As the foam stabilizer, any commonly used foam stabilizer can be used. For example, a silicon-based foam stabilizer such as methylsiloxane emulsion, methylsiloxane, and xylene solution, a fluorine-based foam stabilizer, a fatty acid condensate, Alkylallyl sulfonates, metal soaps of oleic acid sericinoleic acid, guanidine salts, quaternary ammonium compounds, aldehyde-amine condensation products and the like can be used.
また、整泡剤の添加量は、特に限定されるものではな
く、必要に応じて適宜調整すればよいが、通常、熱可塑
性合成樹脂発泡層30を構成する熱可塑性樹脂100重量部
に対して、0.1〜25重量部である。Further, the addition amount of the foam stabilizer is not particularly limited, may be appropriately adjusted as necessary, usually, to 100 parts by weight of the thermoplastic resin constituting the thermoplastic synthetic resin foam layer 30. , 0.1 to 25 parts by weight.
なお、熱可塑性合成樹脂発泡層30の発泡倍率は、通
常、1.2〜5倍、好ましくは1.5〜3倍程度である。The expansion ratio of the thermoplastic synthetic resin foam layer 30 is usually 1.2 to 5 times, preferably 1.5 to 3 times.
さらに、熱可塑性合成樹脂発泡層30は、熱可塑性合成
樹脂層20と同様に、必要に応じて帯電防止性可塑剤およ
び/または帯電防止剤を混入して形成させることもで
き、そのほか可塑剤、安定剤、充填剤、粘度調整剤、発
泡剤、防黴剤、着色剤などの配合剤を添加することも可
能である。Further, the thermoplastic synthetic resin foam layer 30 can be formed by mixing an antistatic plasticizer and / or an antistatic agent, if necessary, similarly to the thermoplastic synthetic resin layer 20, and other plasticizers, It is also possible to add compounding agents such as stabilizers, fillers, viscosity modifiers, foaming agents, antifungal agents and colorants.
さらに、熱可塑性合成樹脂発泡層30の厚みは、0.5〜5
mmが好ましく、0.5mm未満のものでは良好なクッション
性が得られず歩行性が悪くなる傾向があり、一方5mmを
超えると反りや収縮が発生し易くなり、あまり好ましく
ない。Furthermore, the thickness of the thermoplastic synthetic resin foam layer 30 is 0.5 to 5
mm is preferable, and if it is less than 0.5 mm, good cushioning properties cannot be obtained and the walking property tends to deteriorate, while if it exceeds 5 mm, warping or shrinkage is likely to occur, which is not so preferable.
なお、クッション性重歩行床材Aの総厚は、1〜5mm
であるのが好ましい。The total thickness of the cushioning heavy walking floor material A is 1 to 5 mm.
It is preferred that
次に、本発明のクッション性重歩行床材の製造方法の
一例を説明すると、基材であるガラス不織布に塩化ビニ
ル樹脂ペーストなどの液状合成樹脂組成物を塗布含浸さ
せ、これを加熱ゲル化させ、次に表面側に着色された塩
化ビニル樹脂ペーストなどの着色液状合成樹脂組成物を
塗布したのち加熱ゲル化させ、次いでこの表面にグラビ
ア印刷法、スクリーン印刷法(ロータリースクリーン印
刷を含む)などの任意の印刷方法で印刷を施して加熱乾
燥させたのち、さらにこの表面に透明性塩化ビニル樹脂
ペーストなどの透明性液状合成樹脂組成物を塗布したの
ち加熱ゲル化させ、一方ガラス不織布裏面に機械発泡さ
せた塩化ビニル樹脂ペーストなどの液状合成樹脂組成物
を塗布し、加熱ゲル化させる。次いで、得られた積層構
造体を前述の機械発泡させた熱可塑性合成樹脂層が溶融
しない加熱条件下で加熱することにより、本発明のクッ
ション性重歩行床材が得られる。このように、積層構造
体を加熱処理することにより、クッション性重歩行床材
の反りや収縮が抑制される。Next, an example of a method for manufacturing the cushioning heavy walking floor material of the present invention will be described. A glass nonwoven fabric as a base material is coated and impregnated with a liquid synthetic resin composition such as a vinyl chloride resin paste, which is then gelled by heating. , Then apply a colored liquid synthetic resin composition such as a colored vinyl chloride resin paste on the surface side and then heat it to gel, and then apply gravure printing, screen printing (including rotary screen printing) to this surface After printing with any printing method and heating and drying, a transparent liquid synthetic resin composition such as a transparent vinyl chloride resin paste is further applied to this surface and then heated to gel, while mechanical foaming is applied to the back surface of the glass nonwoven fabric. A liquid synthetic resin composition such as the above-mentioned vinyl chloride resin paste is applied and gelled by heating. Next, the cushioned heavy walking floor material of the present invention is obtained by heating the obtained laminated structure under a heating condition in which the mechanically foamed thermoplastic synthetic resin layer does not melt. In this way, by heating the laminated structure, the cushioning heavy walking floor material is prevented from warping and contracting.
また、本発明のクッション性重歩行床材は、機械発泡
させた熱可塑性合成樹脂層の裏面に、更に塩化ビニル樹
脂シートを積層することもできる。この場合、ガラス不
織布裏面側に、機械発泡した液状合成樹脂組成物を塗布
したのち、この液状合成樹脂組成物がゲル化しないうち
に、塩化ビニル樹脂シートを貼着し、加熱ゲル化するこ
ともできるし、ゲル化したのちに塩化ビニル樹脂シート
を貼り合わせる(ドライラミネート法、ウエットラミネ
ート法のいずれでもよい)こともできる。Further, in the cushioned heavy walking floor material of the present invention, a vinyl chloride resin sheet may be further laminated on the back surface of the thermoplastic synthetic resin layer mechanically foamed. In this case, after applying the mechanically foamed liquid synthetic resin composition to the back surface side of the glass nonwoven fabric, a vinyl chloride resin sheet may be attached and gelled by heating before the liquid synthetic resin composition does not gel. Alternatively, after gelling, a vinyl chloride resin sheet may be attached (either a dry laminating method or a wet laminating method may be used).
塩化ビニル樹脂シートを貼り合わせた場合には、クッ
ション性重歩行床材の反りを更に抑制することができ
る。When a vinyl chloride resin sheet is attached, warp of the cushioned heavy walking floor material can be further suppressed.
以下、説明してきたように本発明のクッション性重歩
行床材によれば、基材層の裏面に機械発泡により形成さ
れた熱可塑性合成樹脂発泡層が積層されているので、従
来の化学発泡により形成された熱可塑性合成樹脂発泡層
が積層されているクッション性重歩行床材に比し、連続
してかかる負荷に対しても熱可塑性合成樹脂発泡層の永
久歪みが殆どなく、所望の歩行性(クッション性)が得
られるとともに、床材の上を人が歩行したりした場合な
どの外的負荷に対しても充分な強度が得られ、従って経
時的に床材のへたりなどが生じるのを防止し、優れた強
度性を有するとともに歩行性にも優れたクッション性重
歩行床材となり、床材としての商品価値をより向上させ
ることが可能となる。As described below, according to the cushioning heavy walking floor material of the present invention, since the thermoplastic synthetic resin foam layer formed by mechanical foaming is laminated on the back surface of the base material layer, the conventional chemical foaming is used. Compared to the cushioning heavy walking floor material in which the formed thermoplastic synthetic resin foam layer is laminated, there is almost no permanent distortion of the thermoplastic synthetic resin foam layer even under continuous load, and the desired walkability is obtained. (Cushioning property) and sufficient strength against external load such as when a person walks on the floor material, so that the floor material may get tired over time. And a cushioning type heavy walking flooring material having excellent strength and walking ability, and the commercial value as a flooring material can be further improved.
また、必要に応じ、導電性物質などを使用することに
より、床材の上で作業をする人や種々の機器などに帯電
した静電気を有効に除去するとともに、機器などからの
漏電による感電などの危険を排除し、安全性の高い床材
を得ることも可能である。In addition, if necessary, by using a conductive material, etc., the static electricity charged to people working on the flooring and various equipment can be effectively removed, and electric shock due to leakage from equipment etc. It is possible to eliminate the danger and obtain a safe floor material.
さらに、本発明のクッション性重歩行床材は、基材層
に柔軟な素材を採用した場合には、表面層の熱可塑性合
成樹脂層とあいまって長尺巻が可能で、柔軟性に富み、
折り曲げても折れないため、施工性にも優れるものであ
る。Furthermore, the cushioning heavy walking floor material of the present invention, when a flexible material is used for the base material layer, enables long winding together with the thermoplastic synthetic resin layer of the surface layer, which is rich in flexibility,
Since it does not break even when bent, it has excellent workability.
さらに、本発明のクッション性重歩行床材の敷設にあ
たっては、例えば長尺シート状態での使用のほか、所定
幅に裁断されたタイル状態のものを一般の施工接着剤
(合成ゴムラテックス系、酢酸ビニル樹脂溶剤系、エポ
キシ樹脂系、アクリルエマルジョン系、EVAエマルジョ
ン系など)、または導電性接着剤を使用してフリーアク
セスフロアの床面に接着することで、フリーアクセスフ
ロア用床表面材としても使用可能である。Further, in laying the cushioning heavy walking floor material of the present invention, for example, in addition to being used in a long sheet state, a tile state cut into a predetermined width is used as a general construction adhesive (synthetic rubber latex type, acetic acid). It can also be used as a floor surface material for a free access floor by adhering it to the floor surface of the free access floor using a vinyl resin solvent-based, epoxy resin-based, acrylic emulsion-based, EVA emulsion-based, or conductive adhesive. It is possible.
本発明のクッション性重歩行床材は、少なくとも基材
層の表面に熱可塑性合成樹脂層が積層され、かつ該基材
層の裏面に機械発泡により形成された熱可塑性合成樹脂
発泡層が積層され、さらに該積層構造体を、機械発泡に
より形成された該熱可塑性合成樹脂発泡層が溶融しない
加熱条件下で加熱してなるので優れた強度を有するとと
もに歩行性にも優れ、更には反りや収縮も抑制されたも
のである。In the cushioned heavy walking floor material of the present invention, a thermoplastic synthetic resin layer is laminated on at least the surface of the base material layer, and a thermoplastic synthetic resin foam layer formed by mechanical foaming is laminated on the back surface of the base material layer. Further, since the laminated structure is heated under a heating condition in which the thermoplastic synthetic resin foam layer formed by mechanical foaming does not melt, it has excellent strength and walking ability, and further warps and shrinks. Is also suppressed.
以下、本発明の実施例を挙げて説明する。 Examples of the present invention will be described below.
実施例1 厚さが0.25mmの繊維組織の緻密なガラス繊維紙上に、
第1表の配合例2の塩化ビニル樹脂ペーストをドクター
ナイフコーターにて0.50mmの厚みで塗布し、加熱炉内で
180℃で1分間加熱ゲル化した。Example 1 On a dense glass fiber paper having a fiber structure having a thickness of 0.25 mm,
Apply the vinyl chloride resin paste of formulation example 2 in Table 1 with a doctor knife coater to a thickness of 0.50 mm and in a heating furnace.
It was gelled by heating at 180 ° C for 1 minute.
次いで、この表面にグラビア印刷機にて所定の模様を
印刷し、第1表の配合例3の塩化ビニル樹脂ペーストを
ドクターナイフコーターにて0.1mmの厚みで塗布し、加
熱炉内で180℃で1分間加熱ゲル化した。Then, a predetermined pattern was printed on this surface with a gravure printing machine, and the vinyl chloride resin paste of formulation example 3 in Table 1 was applied with a doctor knife coater to a thickness of 0.1 mm, and at 180 ° C in a heating furnace. It gelled by heating for 1 minute.
次に、上記塩化ビニル樹脂ペーストの塗布面と反対側
の面に、第1表の配合例1の塩化ビニル樹脂ペーストに
圧搾空気を吹き込んでミキサーで攪拌し、小気泡が全体
に分散した液状フォームをドクターナイフコーターにて
0.50mmの厚みで塗布し、加熱炉内で180℃で2分間加熱
ゲル化し、熱可塑性合成樹脂発泡層を形成し、更に該熱
可塑性合成樹脂発泡層が溶融しない加熱条件下にて加熱
(加熱炉内で160℃で2分間加熱したのち、遠赤外線ヒ
ーターにて30秒間加熱)して、冷却後巻き取ることによ
り総厚1.35mmのクッション性重歩行床材を得た。Next, on the surface opposite to the surface coated with the vinyl chloride resin paste, compressed air was blown into the vinyl chloride resin paste of Formulation Example 1 in Table 1 and the mixture was stirred with a mixer to obtain a liquid foam in which small bubbles were dispersed throughout. At the doctor knife coater
It is applied with a thickness of 0.50 mm, heated and gelled at 180 ° C for 2 minutes in a heating furnace to form a thermoplastic synthetic resin foam layer, and further heated under heating conditions in which the thermoplastic synthetic resin foam layer does not melt (heating After heating in a furnace at 160 ° C. for 2 minutes, heating with a far infrared heater for 30 seconds), cooling and winding up, a cushioning heavy walking floor material with a total thickness of 1.35 mm was obtained.
なお、熱可塑性合成樹脂発泡層が溶融しない加熱条件
下での加熱方法としては、上記に限定されるものではな
く、例えば、加熱炉またはそれに類する加熱装置にて13
0〜190℃で0.5〜10分間加熱する方法、遠赤外線ヒータ
ーまたはそれに類する加熱装置にて10〜180秒間加熱す
る方法、あるいは必要に応じて両者を併用する方法など
であってもよい。The heating method under the heating condition in which the thermoplastic synthetic resin foam layer does not melt is not limited to the above, and for example, in a heating furnace or a similar heating device 13
It may be a method of heating at 0 to 190 ° C. for 0.5 to 10 minutes, a method of heating at a far infrared heater or a similar heating device for 10 to 180 seconds, or a method of using both of them together if necessary.
次に、このクッション性重歩行床材の耐磨耗性をテー
パ式磨耗試験でS−42のサンドペーパーを使用して試験
を行ったところ、10,000回でも磨耗が殆どなく好ましい
ものであった。Next, the abrasion resistance of this cushioning heavy walking floor material was tested by a taper type abrasion test using S-42 sandpaper. As a result, there was almost no abrasion even after 10,000 times, and it was preferable.
また連続して8kg/25cm2の負荷(80kgの体重に相当す
る負荷)を10秒間隔で12時間作用させ、12時間は負荷を
かけない強度試験を100日間にわたり行ったところ、へ
たりは全く生ぜず良好なクッション性を示すものであっ
た。In addition, a load of 8 kg / 25 cm 2 (load equivalent to 80 kg of body weight) was continuously applied for 12 hours at 10 second intervals, and a strength test was performed for 12 hours without applying a load for 100 days. It did not produce any good cushioning properties.
第1図は本発明のクッション性重歩行性床材の拡大断面
図である。 10;基材層 20;熱可塑性合成樹脂層 30;熱可塑性合成樹脂発泡層FIG. 1 is an enlarged cross-sectional view of the cushioning heavy walking floor material of the present invention. 10; Base material layer 20; Thermoplastic synthetic resin layer 30; Thermoplastic synthetic resin foam layer
Claims (1)
脂層が積層され、かつ該基材層の裏面には機械発泡によ
り形成された熱可塑性合成樹脂発泡層が積層された積層
構造体からなり、該積層構造体を該熱可塑性合成樹脂発
泡層が溶融しない加熱条件下で加熱してなるクッション
性重歩行床材。1. A laminate structure in which a thermoplastic synthetic resin layer is laminated on at least the surface of a base material layer, and a thermoplastic synthetic resin foam layer formed by mechanical foaming is laminated on the back surface of the base material layer. And a cushioning heavy walking floor material obtained by heating the laminated structure under heating conditions in which the thermoplastic synthetic resin foam layer does not melt.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2107673A JPH0830310B2 (en) | 1990-04-25 | 1990-04-25 | Cushioning heavy walking floor material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2107673A JPH0830310B2 (en) | 1990-04-25 | 1990-04-25 | Cushioning heavy walking floor material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0411082A JPH0411082A (en) | 1992-01-16 |
| JPH0830310B2 true JPH0830310B2 (en) | 1996-03-27 |
Family
ID=14465096
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2107673A Expired - Fee Related JPH0830310B2 (en) | 1990-04-25 | 1990-04-25 | Cushioning heavy walking floor material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0830310B2 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001140458A (en) * | 1999-11-16 | 2001-05-22 | Lonseal Corp | Floor covering |
| JP2003001922A (en) * | 2001-06-25 | 2003-01-08 | Toppan Forms Co Ltd | Manufacturing method of forgery prevention sheet using glossy ink |
| JP2003001923A (en) * | 2001-06-25 | 2003-01-08 | Toppan Forms Co Ltd | Manufacturing method of anti-counterfeit sheet having projections |
| JP6031401B2 (en) * | 2013-04-16 | 2016-11-24 | フクビ化学工業株式会社 | Flooring |
| JP6841582B2 (en) * | 2014-09-29 | 2021-03-10 | 東リ株式会社 | Interior sheet for bathroom, and wall or ceiling structure of bathroom |
| JP2020041327A (en) * | 2018-09-11 | 2020-03-19 | アキレス株式会社 | Floor material and production method thereof |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4928662A (en) * | 1972-07-12 | 1974-03-14 | ||
| JPS563947U (en) * | 1979-06-22 | 1981-01-14 | ||
| JPS5622870A (en) * | 1979-08-03 | 1981-03-04 | Kohkoku Chem Ind | Laminated floor material |
| JPS603988A (en) * | 1983-06-22 | 1985-01-10 | Ishikawajima Harima Heavy Ind Co Ltd | Metal plate coating joining method using diffusion bonding |
| JPS61130350A (en) * | 1984-11-30 | 1986-06-18 | Nippon Zeon Co Ltd | Mechanically foamable plastisol composition |
| JPS6410627A (en) * | 1987-07-02 | 1989-01-13 | Nec Corp | Apparatus for manufacturing semiconductor device |
-
1990
- 1990-04-25 JP JP2107673A patent/JPH0830310B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0411082A (en) | 1992-01-16 |
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