JP4595066B2 - Anti-slip treatment method for lining plate and lining plate therefor - Google Patents
Anti-slip treatment method for lining plate and lining plate therefor Download PDFInfo
- Publication number
- JP4595066B2 JP4595066B2 JP11243297A JP11243297A JP4595066B2 JP 4595066 B2 JP4595066 B2 JP 4595066B2 JP 11243297 A JP11243297 A JP 11243297A JP 11243297 A JP11243297 A JP 11243297A JP 4595066 B2 JP4595066 B2 JP 4595066B2
- Authority
- JP
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- Prior art keywords
- lining plate
- polyurethane resin
- resin
- slip
- treatment method
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 16
- 229910000831 Steel Inorganic materials 0.000 claims description 20
- 229920005749 polyurethane resin Polymers 0.000 claims description 20
- 239000010959 steel Substances 0.000 claims description 20
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 230000000704 physical effect Effects 0.000 claims description 3
- 238000010998 test method Methods 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 27
- 239000000463 material Substances 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 11
- 238000000576 coating method Methods 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 9
- 239000004576 sand Substances 0.000 description 9
- 239000000377 silicon dioxide Substances 0.000 description 9
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
- -1 aromatic polyol Chemical class 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- OIAUFEASXQPCFE-UHFFFAOYSA-N formaldehyde;1,3-xylene Chemical compound O=C.CC1=CC=CC(C)=C1 OIAUFEASXQPCFE-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000004567 concrete Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 229930185605 Bisphenol Natural products 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- 229920005903 polyol mixture Polymers 0.000 description 3
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 2
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 2
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 2
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002184 metal Substances 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
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- 239000005059 1,4-Cyclohexyldiisocyanate Substances 0.000 description 1
- JRQLZCFSWYQHPI-UHFFFAOYSA-N 4,5-dichloro-2-cyclohexyl-1,2-thiazol-3-one Chemical compound O=C1C(Cl)=C(Cl)SN1C1CCCCC1 JRQLZCFSWYQHPI-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Chemical group CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 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
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000009412 basement excavation Methods 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009429 electrical wiring Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003973 paint 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
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Landscapes
- Road Paving Structures (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
Description
【0001】
【産業上の利用分野】
本発明は、作業性、長期の防滑性に優れる仮設道路用として用いる覆工板の防滑処理方法およびその覆工板に関する。
【0002】
【従来の技術】
現在、社会基盤のより一層の整備を図るために地下鉄、上下水道、ガス導管、電気配線、高速道路等の工事が、大都市を中心に盛んに行われている。これら地下工事に伴う道路掘削により、仮設用道路としてH型鋼をベースにした覆工板が使用されている。この覆工板の鋼板表面は格子模様などの突起を付けた防滑機能が施されているが、騒音、湿潤時の防滑性を満足させていない。そこで一般には覆工板の鋼板表面に、更にコンクリート又はコンクリートモルタル或いはアスファルトやエポキシ樹脂を用いて表面被覆処理をする方法が採られている。
【0003】
【発明が解決しようとする課題】
しかし、被覆処理によって騒音の低減、防滑性の改善効果は見られるが前者のコンクリート又はコンクリートモルタルは割れ、欠けにより長期の耐久性に問題があり、後者のアスファルトは柔軟性は有るが、鋼板への接着性と塗膜強度が乏しいことによる剥がれ、摩耗等が生じ易く、やはり耐久性が劣るとされている。エポキシ樹脂は、比較的良好であるが耐摩耗性が不足することに加えて、低温下の硬化性が遅く冬期の被覆処理には時間を要して、生産効率の低下を招く欠点を有している。
【0004】
また、二液性常温硬化型ポリウレタン樹脂を用いて鋼材表面の滑り止めを行う方法も採られているが、これらの方法は大抵鋼材表面にポリウレタン樹脂と鋼材が接着するようにプライマー処理が施された後、ポリウレタン樹脂が塗布され種々の防滑処理方法が行われている。該ポリウレタン樹脂は一般塗り床材として用いられている硬さが、JISD硬度計で35〜40のもので、鋼材表面との接着性を確保するためにはプライマーの使用が必須なものである。また、プライマーを使用した該処方に於いてすら鋼板との接着性が不足し、被覆層が剥がれ易く長期の過酷な使用に耐られないことから、この分野で殆ど使用されていない。
【0005】
【課題を解決するための手段】
本発明者らは、これらの欠点を改良するために、ポリウレタン樹脂を用いた覆工板の表面防滑処理方法の開発に取り組み本発明を完成するに至った。
【0006】
即ち、本発明は、鋼製覆工板表面にプライマーを塗布しないで、硬化物の物性がショアーD硬度50以上の二液性常温硬化型ポリウレタン樹脂を塗布し、該ポリウレタン樹脂の硬化する前に骨材を表面に散布し、該ウレタン樹脂が硬化後ポリウレタン樹脂に接着していない骨材を取り除くことを特徴とする覆工板の防滑処理方法、好ましくは二液性常温硬化型ポリウレタン樹脂は、固形分90重量%以上で、硬化物の物性が、JIS K−6301に準拠する試験方法で伸度10%以上の性能を有するものであること、好ましくは骨材は、無機性又は有機性骨材で、その平均粒径が0.2〜2.0mmのものが50重量%以上含まれていること、及びこれらの防滑処理方法で処理されたことを特徴とする覆工板を提供するものである。
【0007】
以下本発明を詳細に説明する。
本発明の覆工板とは、各種土木工事の路面覆工、土木建築現場の仮設桟橋の覆工等に使用されるもので、厚み5〜15mm程度の溝型鋼、H形鋼等を数本突き合わせて溶接し端部四面を鋼板で完全密閉もしくは一部密閉するか、密閉しないものであり、又、中央部には、リブを溶接し補強構造をとっており、表面には、丸模様、四角模様、格子模様等の凹凸が圧延されている鋼板面のものである。回収された覆工板において表層にセメントモルタル等で表面舗装されたものは、それを取り除き鋼板面を出したものである。
【0008】
二液性常温硬化型ポリウレタン樹脂としては、硬化物の物性がショアーD硬度50以上、好ましくは固形分90重量%以上で、JIS K6301(加流ゴム物理試験方法)伸度10%以上の性能を有するものである。特に好ましくは、固形分92〜100%、ショアーD硬度60〜90、伸度30〜250%の範囲の樹脂が良い。常温とは、JIS K 0050で15〜25℃を示す。
【0009】
本発明で使用する二液性常温硬化型ポリウレタン樹脂とは、好ましくは水酸基を2個以上有する水酸基当量50以上の芳香族系ポリオールを必須成分として含有するポリオール混合物(A)、分子中に2個以上の遊離のイソシアナート基を有するポリイソシアナート化合物(B)とからなる樹脂であり、必要に応じ、溶媒、触媒、顔料等を配合せしめたものからなるものである。
【0010】
本発明の芳香族系ポリオール(A)とは、好ましくは末端に水酸基2個以上有し芳香環を複数有する直鎖状化合物で、例えばキシレンホルムアルデヒド樹脂、ビスフェノール樹脂、ノボラック樹脂等の芳香族樹脂、ビスフェノールA、ビスフェノールB等の芳香族化合物の末端にエチレンオキサイド、プロピレンオキサイド等のアルキルオキサイドを付加させたもの、及びその様なものを水添させた脂環族系樹脂、フタル酸にエチレングリコールを反応させた樹脂などの、水酸基を2個以上有するポリオール混合物を好ましく使用するものである。
【0011】
キシレンホルムアルデヒド樹脂とはメタキシレンとホルムアルデヒドとの反応によって得られるオリゴマー及びそれに第三成分(アミノ基含有化合物、不飽和基含有化合物)を反応させたオリゴマーである。
【0012】
ノボラック樹脂とは、フェノール類とホルムアルデヒドとの反応によって得られるオリゴマー及びそれに第三成分(アミノ基含有化合物、不飽和基含有化合物)を反応させたオリゴマーである。
【0013】
ビスフェノール樹脂とは、ビスフェノール化合物類であり、用いられるビスフェノール類としては、ビスフェノールA〔2,2'-ビス(4−ヒドロキシフエニル)プロパン〕、ビスフェノールB〔2,2'-ビス(4-ヒドロキシフエニル)ブタン〕、ビスフェノールF〔2,2'−(4ーヒドロキシフエニル)メタン〕、ビスフェノールS〔2、2'-(4−ヒドロキシフエニル)スルホン〕および2,2'-(4−ヒドロキシフエニル)ヘキサフルオロプロパンがあげられる。
【0014】
更に、本発明のポリオール(A)は、好ましくはポリオール型キシレンホルムアルデヒド樹脂であってもよく、その構造はメタキシレンが、アルキレン、アセタールまたはエーテル結合により結ばれ、末端にキシレン核及びメチロール基やメトキシメチル基を含有する多分子構造のものである。このポリオール型キシレンホルムアミド樹脂は、メタキシレンとホルマリンとを強酸触媒下で反応させて得られるキシレンホルムアルデヒド樹脂の末端にメチロール基またはメトキシメチル基等を導入することにより得られる。またさらにこのキシレンホルムアルデヒド樹脂中の反応性に富んだ上記の結合基や末端基に、フェノール類、カルボン酸、アミン、アルコール、あるいは芳香族炭化水素など活性水素を有する化合物を1種類もしくは2種以上を含有するものであってもよい。
【0015】
2個以上の遊離のイソシアナート基を有するイソシアナート化合物(B)とは、2,4および2,6トルエンジイソシアネート(TDI)、ジフェニルメタン4,4’ージイソシアネート(ピュアーまたはモノメリックMDI)、ポリメリックMDI、クルードMDI、ヘキサメチレンジイソシアネート(HDI)、トランスーシクロヘキサ1,4ージイソシアネート(CHDI)、イソホロンジイソシアネート(IPDI)、m−キシレンジイソシアネート(XDI)、ナフタレンジイソシアネート(NDI)、p−フェニレンジイソシアネート(PPDI)、4,4’ージフェニルメタントリイソシアネート(デスモジュールRI)、及びこれらイソシアネート化合物と活性水素含有化合物とのNCO末端プレポリマー(プレポリマー化)、およびカルボジイミド化等により液状化された変性ポリイソシアネートなどのポリイソシアネート化合物である。
【0016】
好ましくは、クルードMDI〔MR−100,MR−200,MR−400(日本ポリウレタン製)〕または変性液状MDI〔アイソネート143L(化成アップジョン製)〕である。
【0017】
骨材としては、樹脂に対する化学的安定性を有し、かつ耐摩耗性のあるものであれば特に制限無く各種材料が使用できる。好ましくは平均粒径が、0.2〜2.0mmの範囲のもので、無機性骨材では珪砂、炭化珪素、カーボンランダム、アルミナ石粒等であり、有機性骨材では例えばFRPの粉砕物、ゴムチップ、木片チップ等が代表的なものとして挙げられる。
【0018】
硬化する前とは、該ウレタン樹脂皮膜に骨材を散布した時に骨材が沈み込みこみができるまでの時間を示し、該ウレタン樹脂の混合粘度が20万cpsに達するまでを言うものである。
【0019】
塗布するとは、該ウレタン樹脂を、吹き付け機、ローラー又はコテ、刷毛等を使用して均一に塗り広げ、物体の表面を該ウレタン樹脂皮膜で被覆することを言うものである。
【0020】
散布するとは、塗布した該ウレタン樹脂皮膜に骨材を手撒き又は、機械撒きによって該ウレタン樹脂皮膜が見えなくなるまで均一に骨材を撒く事を言うものである。
【0021】
本発明の防滑処理方法は、初めて防滑処理を行う覆工板であれば何も処理しなくても良い場合もあるが、好ましくは表面の取れ易い錆、塗料、油等の異物を簡単なブラスト処理で取り除き、表面を乾燥させるのが良い。該表面に二液性常温硬化型ポリウレタン樹脂を好ましくは平均塗布厚さ0.2〜5.0mm、より好ましくは0.5〜2.0mmになるように塗布し、該ポリウレタン樹脂が硬化しない内に、その表面に好ましくは平均粒径が0.2〜2.0mmの無機性又は有機性骨材を該ポリウレタン樹脂が隠れる程過剰量を散布する。更に、該ポリウレタン樹脂が硬化後、接着していない骨材を箒、掃除機等によって取り除き、防滑性の覆工板を得る。
【0022】
以下実施例によりさらに詳細に説明する。なお、実施例中重量基準は「部」で示す。
【0023】
実施例1
覆工板表面にウレタン樹脂(大日本インキ化学工業製:プライアデックHF3000 諸物性は以下の表1、2に示す)にて2mmになるようローラーで塗布し、すぐに、珪砂3号を被覆材が見えなくなるまで散布する。24時間自然乾燥後、余分な珪砂を取り除き、防滑層を形成させた。
【0024】
プライアデックHF3000の概略
水酸基を2個以上有する水酸基当量50以上のポリオール型キシレンホルムアルデヒド樹脂を必須成分として含有するポリオール混合物(A)、と分子中に2個以上の遊離のイソシアナート基を有するポリイソシアナート化合物(B)とからなるウレタン系硬質組成物。
【0025】
【表1】
【0026】
【表2】
【0027】
【0028】
実施例2
覆工板表面にショアーD硬度85ウレタン樹脂にて2mmになるようローラーで塗布し、すぐに、珪砂3号を被覆材が見えなくなるまで散布する。24時間自然乾燥後、余分な珪砂を取り除き、防滑層を形成させた。
【0029】
【0030】
比較例1
覆工板表面に被覆材(タールエポキシ樹脂:配合比=1/1 可使時間20分)にて2mmになるようローラーで塗布し、すぐに、珪砂3号を被覆材が見えなくなるまで散布する。24時間自然乾燥後、余分な珪砂を取り除き、防滑層を形成させた。
【0031】
【0032】
比較例1
覆工板表面に被覆材(エポキシ樹脂:配合比=2/1 可使時間30分)にて2mmになるようローラーで塗布し、すぐに珪砂3号を被覆材が見えなくなるまで散布する。24時間自然乾燥後余分な珪砂を取り除き、防滑層を形成させた。
【0033】
【0034】
実施例1〜2及び比較例1〜2で得られた試験板につき、建材試験センターに付着強さを測定したところ表3の通りであった。実際の道路に置き、観察した結果は、表4の通りであった。
【0035】
【表3】
【0036】
【表4】
【0037】
表3より、本発明による実施例においては、接着性は比較例に比べて優れており、すべて材料破壊となっている。また、表4からは、実施例においては、1年後においてもニート層には異常なく優れた防滑性能を有していた。比較例1では4ヶ月後には、クラックが発生し、剥離している常態で、1年後には、ほとんど剥離していた。
【0038】
【発明の効果】
本発明は、覆工板の防滑処理方法において(1)鋼板の表面にプライマーを塗布することなく、(2)鋼板の表面に直接二液性常温硬化型ポリウレタン樹脂を塗布した後、(3)骨材を散布して防滑面を得る方法である。即ち、プライマーを塗布するという面倒でコストのかかる工程が省略でき、それでいて鋼材表面に堅固に接着して長期の耐久性を有する防滑表面を得ることができる。
【0039】
本発明により得られる覆工板の防滑層は、プライマー無しでも鋼板と接着性が高く、伸びがあるために、まず、覆工板の金属表面の被覆膜となり、金属の劣化を防ぎ、次に、ニート層のヒビ割れ、剥離が生じにくくなり、その結果、長期間の接着性、滑り止め効果を保持できるものである。[0001]
[Industrial application fields]
The present invention relates to an anti-slip treatment method for a lining board used for a temporary road having excellent workability and long-term anti-slip property, and the lining board.
[0002]
[Prior art]
Currently, construction of subways, water and sewage systems, gas conduits, electrical wiring, highways, etc. is being actively conducted in large cities in order to further improve the social infrastructure. Due to road excavation accompanying these underground works, lining plates based on H-shaped steel are used as temporary roads. The steel plate surface of the lining plate is provided with an anti-slip function having protrusions such as a lattice pattern, but does not satisfy the anti-slip property when it is noisy and wet. Therefore, in general, a method of applying a surface covering treatment to the steel plate surface of the lining plate using concrete, concrete mortar, asphalt or epoxy resin is employed.
[0003]
[Problems to be solved by the invention]
However, the coating treatment can reduce noise and improve anti-slip properties, but the former concrete or concrete mortar has problems with long-term durability due to cracking and chipping, and the latter asphalt is flexible, It is said that the durability and the durability are inferior due to easy peeling and wear due to the poor adhesion and coating strength. Epoxy resins are relatively good but have a shortage of wear resistance. In addition, they have the disadvantages of low curability at low temperatures and slow time for winter coating, leading to reduced production efficiency. ing.
[0004]
In addition, methods for preventing slippage of the steel surface using a two-component room temperature curing type polyurethane resin are also employed, but these methods are usually subjected to a primer treatment so that the polyurethane resin and the steel material adhere to the surface of the steel material. Thereafter, a polyurethane resin is applied and various anti-slip treatment methods are performed. The polyurethane resin has a hardness of 35 to 40 according to a JISD hardness meter used as a general coating floor material, and a primer is indispensable in order to ensure adhesion to the steel material surface. Moreover, even in the prescription using a primer, the adhesiveness with a steel plate is insufficient, and the coating layer is easily peeled off and cannot be used for a long period of severe use. Therefore, it is hardly used in this field.
[0005]
[Means for Solving the Problems]
In order to improve these drawbacks, the present inventors have worked on the development of a surface anti-slip treatment method for a lining plate using a polyurethane resin, and have completed the present invention.
[0006]
That is, in the present invention, before applying the primer on the surface of the steel lining plate, before applying the two-component room temperature curing type polyurethane resin having a cured product having a Shore D hardness of 50 or more and curing the polyurethane resin. An anti-slip treatment method for a lining board, characterized in that the aggregate is spread on the surface and the urethane resin is cured and the aggregate not adhered to the polyurethane resin is removed, preferably a two-component room temperature curing polyurethane resin, The solid content is 90% by weight or more, and the physical properties of the cured product have a performance of elongation of 10% or more by a test method according to JIS K-6301. Preferably, the aggregate is an inorganic or organic bone. The present invention provides a lining plate characterized by containing 50% by weight or more of a material having an average particle size of 0.2 to 2.0 mm and having been treated by these anti-slip treatment methods.
[0007]
The present invention will be described in detail below.
The lining board of the present invention is used for road surface lining of various civil engineering works, lining of temporary piers at civil engineering construction sites, etc., and several pieces of grooved steel, H-shaped steel, etc. having a thickness of about 5 to 15 mm. Welded and welded, and the end four sides are either completely sealed or partially sealed with steel plate, or not sealed, and the center part is welded with a rib and has a reinforcing structure, the surface has a round pattern, It is a steel plate surface on which irregularities such as a square pattern and a lattice pattern are rolled. In the recovered lining plate, the surface layer is paved with cement mortar or the like, and the surface is removed to remove the steel plate surface.
[0008]
As a two-component room temperature curable polyurethane resin, the cured product has a Shore D hardness of 50 or more, preferably a solid content of 90% by weight or more, and a JIS K6301 (additive rubber physical test method) elongation of 10% or more. It is what you have. Particularly preferred is a resin having a solid content of 92 to 100%, a Shore D hardness of 60 to 90, and an elongation of 30 to 250%. The normal temperature indicates 15 to 25 ° C. according to JIS K 0050.
[0009]
The two-component room temperature curable polyurethane resin used in the present invention is preferably a polyol mixture (A) containing, as an essential component, an aromatic polyol having two or more hydroxyl groups and a hydroxyl equivalent weight of 50 or more, two in the molecule. It is a resin comprising the above-described polyisocyanate compound (B) having a free isocyanate group, and is obtained by blending a solvent, a catalyst, a pigment and the like as required.
[0010]
The aromatic polyol (A) of the present invention is preferably a linear compound having two or more hydroxyl groups at the terminal and having a plurality of aromatic rings, for example, aromatic resins such as xylene formaldehyde resin, bisphenol resin, novolac resin, A product obtained by adding an alkyl oxide such as ethylene oxide or propylene oxide to the end of an aromatic compound such as bisphenol A or bisphenol B, or an alicyclic resin obtained by hydrogenating such a product, or ethylene glycol added to phthalic acid. A polyol mixture having two or more hydroxyl groups, such as a reacted resin, is preferably used.
[0011]
The xylene formaldehyde resin is an oligomer obtained by the reaction of meta-xylene and formaldehyde and an oligomer obtained by reacting it with a third component (an amino group-containing compound or an unsaturated group-containing compound).
[0012]
The novolak resin is an oligomer obtained by reacting phenols with formaldehyde and an oligomer obtained by reacting a third component (an amino group-containing compound or an unsaturated group-containing compound).
[0013]
Bisphenol resins are bisphenol compounds, and bisphenols used include bisphenol A [2,2′-bis (4-hydroxyphenyl) propane], bisphenol B [2,2′-bis (4-hydroxy). Phenyl) butane], bisphenol F [2,2 ′-(4-hydroxyphenyl) methane], bisphenol S [2,2 ′-(4-hydroxyphenyl) sulfone] and 2,2 ′-(4- Hydroxyphenyl) hexafluoropropane.
[0014]
Furthermore, the polyol (A) of the present invention may preferably be a polyol-type xylene formaldehyde resin, the structure of which is metaxylene linked by an alkylene, acetal or ether bond, and the terminal is a xylene nucleus and a methylol group or methoxy. It has a multimolecular structure containing a methyl group. This polyol type xylene formamide resin can be obtained by introducing a methylol group or a methoxymethyl group at the end of a xylene formaldehyde resin obtained by reacting meta-xylene and formalin in the presence of a strong acid catalyst. Furthermore, one or two or more compounds having active hydrogen such as phenols, carboxylic acids, amines, alcohols, or aromatic hydrocarbons in the above-mentioned reactive bonding groups and terminal groups in the xylene formaldehyde resin. May be contained.
[0015]
The isocyanate compound (B) having two or more free isocyanate groups includes 2,4 and 2,6 toluene diisocyanate (TDI), diphenylmethane 4,4′-diisocyanate (pure or monomeric MDI), polymeric MDI. , Crude MDI, hexamethylene diisocyanate (HDI), trans-cyclohexa-1,4-diisocyanate (CHDI), isophorone diisocyanate (IPDI), m-xylene diisocyanate (XDI), naphthalene diisocyanate (NDI), p-phenylene diisocyanate (PPDI) ), 4,4′-diphenylmethane triisocyanate (Desmodur RI), and NCO-terminated prepolymers of these isocyanate compounds and active hydrogen-containing compounds (prepolymerization) And a carbodiimide, etc. polyisocyanate compounds such as liquid modified polyisocyanate.
[0016]
Crude MDI [MR-100, MR-200, MR-400 (manufactured by Nippon Polyurethane)] or modified liquid MDI [Isonate 143L (made by Kasei Upjohn)] is preferable.
[0017]
As the aggregate, various materials can be used without particular limitation as long as they have chemical stability to the resin and are wear resistant. Preferably, the average particle diameter is in the range of 0.2 to 2.0 mm, inorganic aggregates are silica sand, silicon carbide, carbon random, alumina stone grains, etc., and organic aggregates are, for example, pulverized FRP, rubber chips, A typical example is wood chip.
[0018]
The term “before curing” refers to the time until the aggregate sinks when the aggregate is sprayed on the urethane resin film, and refers to the time until the mixed viscosity of the urethane resin reaches 200,000 cps.
[0019]
Applying means that the urethane resin is uniformly spread using a spraying machine, a roller or a trowel, a brush or the like, and the surface of the object is covered with the urethane resin film.
[0020]
“Sprinkling” means that the aggregate is evenly spread until the urethane resin film becomes invisible by hand or mechanically spreading the applied urethane resin film.
[0021]
In the anti-slip treatment method of the present invention, there is a case where no treatment is required as long as it is the first lining plate to be subjected to the anti-slip treatment. However, it is preferable that a foreign matter such as rust, paint, oil, etc., whose surface is easily removed, be simply blasted. It is better to remove by treatment and dry the surface. A two-component room temperature curable polyurethane resin is preferably applied to the surface so that the average coating thickness is 0.2 to 5.0 mm, more preferably 0.5 to 2.0 mm, and the polyurethane resin is not cured. Further, an excessive amount of inorganic or organic aggregate having an average particle diameter of 0.2 to 2.0 mm is spread on the surface so that the polyurethane resin is hidden. Further, after the polyurethane resin is cured, the non-adhered aggregate is removed with a scissors, a vacuum cleaner or the like to obtain an anti-slip lining plate.
[0022]
Examples will be described in more detail below. In the examples, the weight standard is indicated by “parts”.
[0023]
Example 1
The surface of the lining plate was coated with a urethane resin (made by Dainippon Ink & Chemicals, Inc .: Praiadec HF3000, the physical properties are shown in Tables 1 and 2 below) with a roller, and immediately, silica sand No. 3 was coated. Spread until no longer visible. After natural drying for 24 hours, excess silica sand was removed to form an anti-slip layer.
[0024]
A polyol mixture (A) containing, as an essential component, a polyol-type xylene formaldehyde resin having a hydroxyl equivalent of 50 or more having two or more hydroxyl groups, and a polyisocyanate having two or more free isocyanate groups in the molecule. A urethane-based hard composition comprising a narate compound (B).
[0025]
[Table 1]
[0026]
[Table 2]
[0027]
[0028]
Example 2
The surface of the lining plate is coated with a roller with a Shore D hardness of 85 urethane resin so as to be 2 mm, and immediately, silica sand No. 3 is sprayed until the coating material becomes invisible. After natural drying for 24 hours, excess silica sand was removed to form an anti-slip layer.
[0029]
[0030]
Comparative Example 1
Apply the coating material (tar epoxy resin: blending ratio = 1/1 usable life 20 minutes) to the surface of the lining plate with a roller so that it becomes 2 mm, and immediately spread silica sand No. 3 until the coating material is no longer visible. . After natural drying for 24 hours, excess silica sand was removed to form an anti-slip layer.
[0031]
[0032]
Comparative Example 1
Apply the coating material (epoxy resin: compounding ratio = 2/1 working life 30 minutes) to the surface of the lining plate with a roller so as to be 2 mm, and immediately spread silica sand No. 3 until the coating material is no longer visible. After natural drying for 24 hours, excess silica sand was removed to form an anti-slip layer.
[0033]
[0034]
It was as Table 3 when the adhesion strength was measured in the building material test center about the test board obtained in Examples 1-2 and Comparative Examples 1-2. Table 4 shows the results of observation on an actual road.
[0035]
[Table 3]
[0036]
[Table 4]
[0037]
From Table 3, in the Example by this invention, adhesiveness is excellent compared with the comparative example, and all are material destruction. Also, from Table 4, in the examples, even after one year, the neat layer had excellent anti-slip performance without abnormality. In Comparative Example 1, cracks occurred after 4 months, and in a normal state where the cracks were peeled off, they were almost peeled off after 1 year.
[0038]
【The invention's effect】
The present invention provides an anti-slip treatment method for a lining plate (1) without applying a primer to the surface of the steel plate, (2) after directly applying a two-component room temperature curing polyurethane resin to the surface of the steel plate, (3) It is a method of obtaining an anti-slip surface by spraying aggregate. That is, the troublesome and costly process of applying the primer can be omitted, and yet a non-slip surface having long-term durability can be obtained by firmly bonding to the steel surface.
[0039]
The anti-slip layer of the lining plate obtained according to the present invention has high adhesion to the steel plate even without a primer and has elongation, so that it first becomes a coating film on the metal surface of the lining plate to prevent metal deterioration, and In addition, cracking and peeling of the neat layer are less likely to occur, and as a result, long-term adhesion and anti-slip effects can be maintained.
Claims (3)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11243297A JP4595066B2 (en) | 1997-04-30 | 1997-04-30 | Anti-slip treatment method for lining plate and lining plate therefor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11243297A JP4595066B2 (en) | 1997-04-30 | 1997-04-30 | Anti-slip treatment method for lining plate and lining plate therefor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH10296181A JPH10296181A (en) | 1998-11-10 |
| JP4595066B2 true JP4595066B2 (en) | 2010-12-08 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11243297A Expired - Lifetime JP4595066B2 (en) | 1997-04-30 | 1997-04-30 | Anti-slip treatment method for lining plate and lining plate therefor |
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| JP (1) | JP4595066B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG108832A1 (en) * | 2001-01-24 | 2005-02-28 | Nippon Paint Co Ltd | Method of fabricating a membranous substance and method of fabricating a multilayer membranous substance |
| JP4826865B2 (en) * | 2001-04-19 | 2011-11-30 | Dic株式会社 | Urethane hard coating resin composition and coating material |
| JP2007023592A (en) * | 2005-07-15 | 2007-02-01 | Nitta Ind Corp | Rubber expansion joint |
| JP7236751B2 (en) * | 2020-06-23 | 2023-03-10 | 株式会社永商興産 | Floorboards with non-slip layer used for temporary passages and construction method for the non-slip layer |
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1997
- 1997-04-30 JP JP11243297A patent/JP4595066B2/en not_active Expired - Lifetime
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| Publication number | Publication date |
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| JPH10296181A (en) | 1998-11-10 |
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