JPH0196079A - Coating of cementitious base material - Google Patents
Coating of cementitious base materialInfo
- Publication number
- JPH0196079A JPH0196079A JP25586987A JP25586987A JPH0196079A JP H0196079 A JPH0196079 A JP H0196079A JP 25586987 A JP25586987 A JP 25586987A JP 25586987 A JP25586987 A JP 25586987A JP H0196079 A JPH0196079 A JP H0196079A
- Authority
- JP
- Japan
- Prior art keywords
- base material
- lining layer
- concrete
- polyester resin
- lining
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 33
- 239000011248 coating agent Substances 0.000 title claims description 9
- 238000000576 coating method Methods 0.000 title claims description 9
- 239000012948 isocyanate Substances 0.000 claims abstract description 23
- 239000011521 glass Substances 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 9
- -1 isocyanate compound Chemical class 0.000 claims description 20
- 239000004568 cement Substances 0.000 claims description 17
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 13
- 230000000704 physical effect Effects 0.000 claims description 7
- 150000002513 isocyanates Chemical class 0.000 abstract description 5
- 229920001225 polyester resin Polymers 0.000 abstract description 4
- 239000004645 polyester resin Substances 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 239000004567 concrete Substances 0.000 description 27
- 239000010410 layer Substances 0.000 description 25
- 239000002585 base Substances 0.000 description 22
- 229920005989 resin Polymers 0.000 description 17
- 239000011347 resin Substances 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 11
- 239000000853 adhesive Substances 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 230000006866 deterioration Effects 0.000 description 5
- 238000005452 bending Methods 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 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 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 230000000149 penetrating effect Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 1
- BTFWJAUZPQUVNZ-UHFFFAOYSA-N 1-methyl-3-[(3-methylphenyl)methyl]benzene Chemical compound CC1=CC=CC(CC=2C=C(C)C=CC=2)=C1 BTFWJAUZPQUVNZ-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229910001294 Reinforcing steel Inorganic materials 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004140 cleaning 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
- 239000002131 composite material Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000011381 foam concrete Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000011414 polymer cement Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 230000009993 protective function Effects 0.000 description 1
- 239000011150 reinforced concrete Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229920001187 thermosetting polymer Polymers 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
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Aftertreatments Of Artificial And Natural Stones (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】 帆1ユ11県り妃1 本発明はセメント系基材の被覆方法に関する。[Detailed description of the invention] sail 1 yu 11 prefecture rihi 1 The present invention relates to a method for coating cement-based substrates.
従来の技術
これ迄、半永久的な耐久性があると云われていたセメン
ト系基材、特に鉄筋コンクリート構造物は期待された程
の性能のないことが判ってきて、コンクリートの耐久性
が改めて問い直されてから久しい。Conventional technology Until now, cement-based base materials, which were said to have semi-permanent durability, and especially reinforced concrete structures, have been found to not have the performance that was expected, and the durability of concrete is being questioned once again. It's been a long time since that happened.
ひび割れや塩害に見られるコンクリート構造物の初期劣
化現象や、老化現象とも云える中性化は耐久消費材とし
ての性格を持つコンクリート構造物にとっては非常に重
大な問題である。Initial deterioration phenomena of concrete structures, such as cracks and salt damage, and carbonation, which can be called aging phenomena, are very serious problems for concrete structures, which are characterized as durable consumer materials.
コンクリートの劣化状況はコンクリートの使用される環
境条件やコンクリートの品質で大きな影響を受けるが、
最近になって明らかにされたコンクリート構造物の劣化
機構はコンクリート自体の劣化によって決まるのではな
く、鉄筋の腐蝕によって支配されるとされている。The state of deterioration of concrete is greatly affected by the environmental conditions in which concrete is used and the quality of concrete.
It has recently been revealed that the deterioration mechanism of concrete structures is not determined by the deterioration of the concrete itself, but is controlled by the corrosion of the reinforcing steel.
一方、コンクリート構造物の劣化対策として保護材に要
求されている基本性能は「道路橋の塩害対策指針(案)
・同解説」によれば
■空気中の酸素、湿気、雨水などの水分、塩化物(塩素
イオン)等の外部からの有害物質の侵入を防止し、
■コンクリートに対して充分な接着力を持ち、コンクリ
ートと一体となって挙動すると共に充分な伸び能力を持
ち、少々のひび割れには追従すること
である。On the other hand, the basic performance required of protective materials to prevent deterioration of concrete structures is based on the ``Guidelines for Salt Damage Countermeasures for Road Bridges (Draft)''.
・According to the same explanation, ■Prevents the intrusion of harmful substances from the outside, such as oxygen in the air, humidity, water such as rainwater, and chloride (chlorine ions), and ■Has sufficient adhesion to concrete. , it behaves as one with the concrete, has sufficient elongation ability, and can follow the slightest cracks.
又コンクリートの表面は単純ではな(、種々の問題を起
こしているのは、コンクリートが本質的に多孔質材料で
あってかなりの不均質性を有していることにある。その
上コンクリートの含水状態は保護材との接着強度に多大
の影響を与えており、表面水分計による含水率が8%以
下と規定されていても8%以下とすることは、α外に困
難であり、少々の水分の存在のもとでも施工が可能なこ
とら材料特性として必要条件の一つである。Moreover, the surface of concrete is not simple (and this causes various problems because concrete is an inherently porous material and has considerable heterogeneity. Furthermore, the water content of concrete The condition has a great effect on the adhesive strength with the protective material, and even if the moisture content is specified to be 8% or less by a surface moisture meter, it is extremely difficult to keep it below 8%, and there may be some This is one of the necessary material properties as it can be applied even in the presence of moisture.
以上のような外部から侵入する耐久性阻害環境要因に対
しての保護材として既に幾通りかの提案がなされている
。Several proposals have already been made as protective materials against the durability-inhibiting environmental factors that invade from the outside.
1、有機質系浸透性防水剤による保護
2、無機質系浸透性防水剤による保護
3、合成樹脂によるコーティング保護
4、レジンモルタル(ポリマーセメント)や防水モルタ
ルによる保護
5、合成樹脂ライニングによる保護
1.2については作業は至って良いが、透湿性(通気性
)が大きいのでその機能の持続性に乏しく、コンクリー
トの中性化抑制にバラツキがあるか、又は殆ど効果が認
められない。1. Protection by organic penetrating waterproofing agent 2. Protection by inorganic penetrating waterproofing agent 3. Coating protection by synthetic resin 4. Protection by resin mortar (polymer cement) or waterproof mortar 5. Protection by synthetic resin lining 1.2 The work is quite good, but because of the high moisture permeability (air permeability), the sustainability of the function is poor, and there are variations in concrete neutralization suppression, or there is almost no effect.
3のコーティングは合成樹脂によっては中性化防止能が
あり、複層吹付など工法上の工夫で機能を発揮していて
、接着力があるもののコンクリート表層のひび割れ追従
性に欠けており、出隅コーナ一部(エラ′))では平坦
部と同じように厚塗が出来難く、膜厚管理に難点がある
。Coating No. 3 has the ability to prevent carbonation depending on the synthetic resin, and is effective through construction methods such as multi-layer spraying, and although it has adhesive strength, it lacks the ability to follow cracks in the concrete surface layer, and it is difficult to prevent protruding corners. As with flat areas, it is difficult to coat thickly on some corners (erra'), making it difficult to control the film thickness.
4の有機質・無機質モルタルは付着力は良いが、熟練度
のいる作業で3と同様にコンクリート表層のひび割れ追
従性には限界がある。The organic/inorganic mortar in No. 4 has good adhesion, but as with No. 3, it requires skill and has a limited ability to follow cracks in the concrete surface layer.
5のライニング樹脂はエボキン系であるのでその接着力
は抜群であるが、伸び率のある樹脂となると耐水性が悪
い為に湿潤状態になった場合、接着力が極端に劣化して
剥離したり、又高粘度(3,000cps、以上)のた
めに作業性には問題がある。The lining resin in No. 5 is Evokin-based, so its adhesive strength is excellent, but resin with a high elongation rate has poor water resistance, so when it gets wet, the adhesive strength deteriorates dramatically and it may peel off. Also, there is a problem in workability due to the high viscosity (3,000 cps or more).
本発明者らはセメント系基けの外部から侵入する水、湿
気、酸素、塩素イオンなどの耐久性阻害要因を遮断し、
しかもセメント系基材との接着力を維持しながらひび割
れ追従性のある相反する性能の対策を長期間にわたって
鋭意検討を重ねた結果、耐水性、耐アルカリ性の優れた
浸透性1反応性シーラーに特定の不飽和ポリエステル樹
脂をガラスマットでライニングする方法が極めて信頼性
の高いことを知見し、この知見にもとづき、本発明を完
成するに至った。The present inventors blocked durability-inhibiting factors such as water, moisture, oxygen, and chloride ions from entering from the outside of the cement base.
Moreover, as a result of intensive long-term research on countermeasures for the conflicting performance of maintaining adhesion to cement base materials and crack followability, we identified a penetrating 1-reactive sealer with excellent water resistance and alkali resistance. It was discovered that the method of lining an unsaturated polyester resin with a glass mat is extremely reliable, and based on this knowledge, the present invention was completed.
問題点を解決するための手段
本発明は、セメント系基材にNCO基1基当個当の分子
量が200以下であるイソシアネート化合物をプライマ
ーとして塗布し、つづいてチョツプドストランドガラス
マットと硬化物の物性が引張り強さ0.5kg/mm”
以上、引張り弾性率50kg/mm″以下、引張り伸び
30%以上である不飽和ポリエステル樹脂を用いてライ
ニング層を作ることを特徴とするセメント系基材の被覆
方法に関する。Means for Solving the Problems The present invention involves coating a cement base material with an isocyanate compound having a molecular weight of 200 or less per NCO group as a primer, and then applying a chopped strand glass mat and a cured product. The physical properties are tensile strength 0.5kg/mm”
The above describes a method for coating a cement base material, which is characterized in that a lining layer is formed using an unsaturated polyester resin having a tensile modulus of 50 kg/mm'' or less and a tensile elongation of 30% or more.
本発明におけるセメント系基材としては、たとえばコン
クリート、モルタル、スレート、発泡コンクリート、珪
酸カルシウム板、炭カル板1石膏板1石綿板などがあげ
られる。Examples of the cement base material in the present invention include concrete, mortar, slate, foamed concrete, calcium silicate board, charcoal board, gypsum board, and asbestos board.
本発明に使用するプライマーとしては、NCO基1基当
個当の分子量が200以下のイソシアネート化合物があ
げられる。このイソシアネート化合物は分子内に活性N
CO基を2個以上有する単量体およびこれから誘導され
る低分子量重合体又はこれらの混合物である。イソシア
ネート化合物が液状である場合はそのままでも用いるこ
とができるが、有機溶媒に溶かし、溶液状にしたものは
低粘度で、セメント系基材の表面に塗布すると基材の多
孔質毛細管中に深く迅速に浸透・拡散して毛細管中の水
分やセメント水和物の水可溶性塩基物、毛細管壁面の不
安定な未水和物などと直ちに反応して疎水性の安定な固
形物を毛細管中に形成する。これにより多孔質の空隙は
親油性となり安定した耐水性のある固形物で充填され、
その充填された深さは塗布量に比例して基材の内面数c
mに及ぶ。Examples of the primer used in the present invention include isocyanate compounds having a molecular weight of 200 or less per NCO group. This isocyanate compound has active N in its molecule.
These are monomers having two or more CO groups, low molecular weight polymers derived therefrom, or mixtures thereof. If the isocyanate compound is in liquid form, it can be used as it is, but when it is dissolved in an organic solvent and made into a solution, it has a low viscosity, and when applied to the surface of a cementitious base material, it quickly penetrates deeply into the porous capillaries of the base material. It penetrates and diffuses into the capillary and immediately reacts with the water in the capillary, water-soluble bases of cement hydrate, and unstable unhydrated substances on the capillary wall to form a stable hydrophobic solid in the capillary. . As a result, the porous voids become lipophilic and are filled with stable, water-resistant solids.
The filled depth is proportional to the amount of coating, and the number of inner surfaces of the base material c
It extends to m.
本発明に使用されるイソシアネート化合物の例をあげる
とたとえばトリレンジイソシアネート(2,472,6
=65/35)、l=リレンジイソシアネート(2,4
/2.6=80/20)、)リレンジイソシアネート(
2,4=100)、ジフェニルメタン−4,4’−ジイ
ソシアネート、3.3’−ジメチルジフェニルメタン〜
4,4′−ジイソシアネート。Examples of isocyanate compounds used in the present invention include tolylene diisocyanate (2,472,6
=65/35), l=lylene diisocyanate (2,4
/2.6=80/20),) lylene diisocyanate (
2,4=100), diphenylmethane-4,4'-diisocyanate, 3,3'-dimethyldiphenylmethane~
4,4'-diisocyanate.
2.4−4リレンジイソシアネートダイマー、メタキシ
レンジイソシアネート、ヘギサメチレン、゜6−ジイソ
シアネート、ポリアリルポリイソシアネートなどのイソ
シアネート単量体があげられる。Isocyanate monomers such as 2.4-4 lylene diisocyanate dimer, meta-xylene diisocyanate, hegyamethylene, 6-diisocyanate, and polyallyl polyisocyanate are mentioned.
NCO基1基当個当の分子量が200を超えたイソシア
ネート化合物を用いた場合、耐水性、保護材との接着性
などの点でよくない。When an isocyanate compound having a molecular weight per NCO group exceeding 200 is used, it is not good in terms of water resistance, adhesion to a protective material, etc.
イソシアネート化合物を有機溶媒に溶かして用いる場合
、有機溶媒としては、イソシアネート基と反応しない、
たとえばベンゼン、トルエンなどの芳香族炭化水素、ア
セトン、メチルエチルケトン。When using an isocyanate compound dissolved in an organic solvent, the organic solvent should be one that does not react with the isocyanate group.
For example, aromatic hydrocarbons such as benzene and toluene, acetone, and methyl ethyl ketone.
メチルイソブチルケトン、シクロヘキサノンなどのケト
ン類、酢酸エチル、酢酸ブヂル、グリコールエーテルの
エステルなどのエステル類、ジクロルメタン、ジクロル
エタン、トリクロルエチレンなどのハロゲン化炭化水素
、ジメチルホルムアミド、イソホロンなどがあげられる
。溶液中のイソシアネート化合物の使用量はイソシアネ
ート化合物および溶媒の種類にもよるが、通常、約50
〜800g/Q程度である。上記溶液には必要に応じて
触媒を添加してもよい。Examples include ketones such as methyl isobutyl ketone and cyclohexanone, esters such as ethyl acetate, butyl acetate, and glycol ether esters, halogenated hydrocarbons such as dichloromethane, dichloroethane, and trichloroethylene, dimethylformamide, and isophorone. The amount of isocyanate compound used in the solution depends on the type of isocyanate compound and solvent, but is usually about 50
It is about 800g/Q. A catalyst may be added to the above solution if necessary.
イソシアネート化合物の塗布量はセメント系基材の種類
や表面状態などによって異なるが、通常、約200g/
m”〜500g/m”程度である。The amount of isocyanate compound applied varies depending on the type of cement base material and surface condition, but it is usually about 200g/approx.
m" to about 500 g/m".
塗布手段としては、たとえばスプレー塗布1刷毛塗り、
ローラー刷毛塗りなどがあげられる。Application methods include, for example, spray application, one brush application,
Examples include roller brush painting.
セメント系基材表面にイソシアネート化合物を施し、硬
化させた後、チョツプドストランドガラスマットと特定
の不飽和ポリエステル樹脂を用いてライニング層を作る
。After applying an isocyanate compound to the surface of the cement base material and curing it, a lining layer is created using chopped strand glass mat and a specific unsaturated polyester resin.
本発明に使用される特定の不飽和ポリエステル樹脂とは
、不飽和ポリエステルとビニル単量体との混合溶解物で
ある。この不飽和ポリエステルは不飽和二塩基酸とグリ
コールあるいはアルキレンオキサイドとを縮重合あるい
は付加重合させて得られる熱硬化性タイプの樹脂で、不
飽和酸の一部を飽和二塩基酸で置き換えてもよい。The specific unsaturated polyester resin used in the present invention is a mixed solution of unsaturated polyester and vinyl monomer. This unsaturated polyester is a thermosetting resin obtained by condensation polymerization or addition polymerization of an unsaturated dibasic acid and glycol or alkylene oxide, and a portion of the unsaturated acid may be replaced with a saturated dibasic acid. .
不飽和二塩基酸としては、たとえば無水マレイン酸、フ
マル酸、イタコン酸などが、飽和二塩基酸としては、た
とえば無水フタル酸、イソフタル酸。Examples of unsaturated dibasic acids include maleic anhydride, fumaric acid, and itaconic acid; examples of saturated dibasic acids include phthalic anhydride and isophthalic acid.
テレフタル酸、アジピン酸などが、グリコール類として
は、たとえばエチレングリコール、ジエチレングリコー
ル、トリエチレングリコール、プロピレングリコール、
ジプロピレングリコール、ブチレングリコール、ネオペ
ンチールグリコールなどが、アルキレンオキサイドとし
ては、たとえばプロピレンオキサイドなどがあげられる
。Examples of glycols include terephthalic acid and adipic acid, and examples of glycols include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol,
Examples of the alkylene oxide include dipropylene glycol, butylene glycol, and neopentyl glycol. Examples of the alkylene oxide include propylene oxide.
ビニル単量体としては、たとえばスチレン、ビニルトル
エン、α−メチルスチレン、メチルメタアクリレートな
どがあげられる。この樹脂には、たとえばメチルエチル
ケトンパーオキサイドなどの室温硬化用の過酸化物とた
とえばコバルト石ケンなどの硬化促進剤などを加える。Examples of vinyl monomers include styrene, vinyltoluene, α-methylstyrene, and methyl methacrylate. To this resin, a peroxide for curing at room temperature, such as methyl ethyl ketone peroxide, and a curing accelerator, such as cobalt soap, are added.
これらの化合物を用いて得られる不飽和ポリエステル樹
脂類の中、本発明に使用することのできる樹脂としては
、不飽和ポリエステル樹脂硬化物(以下樹脂硬化物と云
う)の物性が引張り強度0.5kg/mm’以上、好ま
しくは1.0kg7mm”以上、引張り弾性率50kg
/mm!以下、好ましくは30kg/mm’以下、引張
り伸び30%以上、好ましくは50%以上を有すること
が必要である。Among the unsaturated polyester resins obtained using these compounds, the resin that can be used in the present invention is a cured unsaturated polyester resin (hereinafter referred to as cured resin) with a tensile strength of 0.5 kg. /mm' or more, preferably 1.0kg7mm'' or more, tensile modulus 50kg
/mm! It is necessary to have a tensile elongation of preferably 30 kg/mm' or less and a tensile elongation of 30% or more, preferably 50% or more.
引張り強さと伸びが上記の値より小さいとライニングし
たセメント系基材にひび割れが発生した場合、ライニン
グ層がひび割れに追随せずにセメント系基材の界面より
剥離したり、ライニング層が破断してセメント系基材の
保護機能が損なわれる。If the tensile strength and elongation are smaller than the above values, if cracks occur in the lined cement base material, the lining layer may not follow the cracks and may separate from the interface of the cement base material, or the lining layer may rupture. The protective function of the cementitious base material is impaired.
ここで、樹tie化物の物性は、3m/m厚みの注形板
を室温で硬化させ、−夜放置後、60℃で!時間、更に
100℃で3時間の後硬化をおこなうことによって試料
を調製し、この試料を曲げ試験はJIS6911.引張
り試験もJ l5691■により測定したものである。Here, the physical properties of the tree tie compound are determined by curing a 3 m/m thick cast plate at room temperature, then leaving it overnight at 60°C. A sample was prepared by further post-curing at 100°C for 3 hours, and the bending test was conducted according to JIS6911. The tensile test was also measured according to Jl5691■.
強化材としてのガラス繊維には種々のタイプがあるが、
本発明ではライニング層として充分な接着力を有し、層
間剥離が発生しにくく、みずみち(水道)にはならない
耐水性があって、全方位にわたって引張り強度が一定し
ているチョツプドストランドガラスマットが用いられる
。ガラスクロス(口抜平IO)は強度は大きいものの、
強さに方向性があり、更に接着強度が劣っている。チョ
ツプドストランドガラスマットは不飽和ポリエステル樹
脂の含浸・脱泡作業の上でも最適である。There are various types of glass fibers used as reinforcing materials.
The present invention uses chopped strand glass as a lining layer, which has sufficient adhesive strength, is resistant to delamination, has water resistance that does not cause drainage, and has constant tensile strength in all directions. A mat is used. Although glass cloth (Kuchinukihira IO) has great strength,
The strength is directional and the adhesive strength is poor. Chopped strand glass mats are also ideal for impregnating and defoaming unsaturated polyester resins.
チョツプドストランドガラスマットは適宜量用いられる
が、通常、約450g/m”のチョツプドストランドガ
ラスマット−枚程度が用いられる。The chopped strand glass mat is used in an appropriate amount, but usually about 450 g/m'' chopped strand glass mat is used.
ライニング時の使用樹脂量は約1−0〜2 、0 kg
/ml11!程度である。また、ライニング層の厚さは
約0.7〜1.5m/m程度である。The amount of resin used during lining is approximately 1-0 to 2.0 kg.
/ml11! That's about it. Further, the thickness of the lining layer is about 0.7 to 1.5 m/m.
ライニング手段としては、たとえばローラー刷毛または
スプレーなどで樹脂を塗布し、ついでローラーなどで樹
脂を含浸・脱泡する手段があげられる。Examples of the lining means include applying a resin with a roller brush or spray, and then impregnating and defoaming the resin with a roller or the like.
このようにしてライニング層を作り、室温で放置すれば
ライニング層中の不飽和ポリエステル樹脂とチョツプド
ストランドガラスマットとの複合体が硬化するとともに
ライニング層とイソシアネート化合物処理されたセメン
ト系基材とが強固に接着される。If the lining layer is made in this way and left at room temperature, the composite of the unsaturated polyester resin and chopped strand glass mat in the lining layer will harden, and the lining layer and the isocyanate compound treated cement base material will harden. is firmly adhered.
発明の効果
本発明によれば、プライマーであるイソシアネート化合
物がセメント系基材に深く浸透、含浸して基材の表層に
躯体防水層を形成し、基材内部のアルカリ成分の溶出を
抑制し、接着力を持続させる機能を有している。Effects of the Invention According to the present invention, the isocyanate compound as a primer deeply penetrates and impregnates the cement base material to form a waterproof layer on the surface layer of the base material, suppressing the elution of alkaline components inside the base material, It has the function of maintaining adhesive strength.
また、低弾性率、高伸び率を有する特定の不飽和ポリエ
ステル樹脂を用いたライニング層は、イソシアネート化
合物を介してセメント系基材と強固に接着しており、高
いゼロスパン強度を持っている。そのため基材のひび割
れ時の追従性がよく、ライニング層のひび割れが発生し
ない。Furthermore, the lining layer made of a specific unsaturated polyester resin with a low modulus of elasticity and high elongation is firmly adhered to the cement base material via an isocyanate compound, and has high zero span strength. Therefore, it has good followability when the base material cracks, and cracks do not occur in the lining layer.
本発明の方法はチョツプドストランドガラスマットを使
ったシームレスライニングであり、複雑な形状でも作業
に問題はなく、セメント系基材を用いた構築物(例、建
物、高速道路、橋梁、床、水槽等)の外表面はもちろん
のこと、天井面にも作業は可能である。また、比較的低
コストの優れた方法である。The method of the present invention is seamless lining using chopped strand glass mat, and there is no problem in working even with complex shapes. It is possible to work not only on the outside surfaces of the walls (e.g.), but also on the ceiling surfaces. It is also an excellent method at relatively low cost.
以下に実施例をあげ、本発明を具体的に説明する。EXAMPLES The present invention will be specifically explained below with reference to Examples.
実施例I
J l5A5304指定市販歩道板コンクリートにイソ
シアネート化合物の塗布および不飽和ポリエステル樹脂
ライニングを行い、室温で1週間放置硬化させた後、常
温の水に浸漬した。浸漬1年後に取り出し、ライニング
層の接着強さおよび接着状態を調べた。Example I J 15A5304 designated commercial sidewalk board concrete was coated with an isocyanate compound and lined with an unsaturated polyester resin, left to harden for one week at room temperature, and then immersed in water at room temperature. After one year of immersion, it was taken out and the adhesive strength and state of the lining layer was examined.
なお用いたイソシアネート化合物は武田薬品工業(株)
製のタケネート300C(NCO基1基当個当の分子量
か135)およびタケネートP−402(NCO基1個
当タリノ分子量が389)。The isocyanate compound used was manufactured by Takeda Pharmaceutical Co., Ltd.
Takenate 300C (molecular weight per NCO group: 135) and Takenate P-402 (molecular weight per NCO group: 389).
ライニング層の不飽和ポリエステル樹脂は武田薬品工業
(株)製、ポリマール8414APである。The unsaturated polyester resin of the lining layer is Polymer 8414AP manufactured by Takeda Pharmaceutical Company Limited.
また8414APの樹脂硬化物の物性は、引張り強さ1
.0kg/mm”、引張り弾性率20kg/mm”。In addition, the physical properties of the cured resin of 8414AP include tensile strength of 1
.. 0kg/mm", tensile modulus of elasticity 20kg/mm".
引張り伸び50%であった。FRPライニング層の厚さ
は約1m/mであった。The tensile elongation was 50%. The thickness of the FRP lining layer was approximately 1 m/m.
試験の結果(表、)より試料の破壊状態、接着強度の保
持性からNo、2.No、4、すなわちNCO基1基当
個当の分子量が200以下のイソシアネート化合物およ
びチョツプドストランドガラスマットの組み合わせのラ
イニングが良好であった。According to the test results (table), No. 2, based on the fracture state of the sample and retention of adhesive strength. The lining of No. 4, a combination of an isocyanate compound having a molecular weight per NCO group of 200 or less and chopped strand glass mat, was good.
実施例2
JISA5307市販コンクリー市販コンクリート境界
ブロック面(150x600mm)に表−2に示した条
件で被覆処理を行った。室温にて7日放置後、ライニン
グ層を引張り側(下面)にして、JISA5307.6
の方法で曲げ試験を行った。Example 2 A JISA5307 commercially available concrete commercially available concrete boundary block surface (150 x 600 mm) was coated under the conditions shown in Table 2. After being left at room temperature for 7 days, the lining layer was placed on the tension side (lower surface) and JISA5307.6
A bending test was conducted using the method.
結果を表−2に示す。The results are shown in Table-2.
なおライニングに使用したポリマール35I7は武田薬
品工業(株)製で、樹脂硬化物の物性は引張り強さ3
、2 kg/ mm” 、引張り弾性率10、 kg/
mm2.引張り伸び23%であった。ライニング層の接
着力が小さいと曲げによる破断箇所がコンクリート基材
の破断箇所と異なる。すなわち、コンクリートとライニ
ング層が一体挙動をとらず、コンクリートのクラック発
生時のライニング層の追随性が充分でないことを示して
いる。Polymer 35I7 used for the lining is manufactured by Takeda Pharmaceutical Co., Ltd., and the physical properties of the cured resin are tensile strength 3.
, 2 kg/mm”, tensile modulus 10, kg/
mm2. The tensile elongation was 23%. If the adhesive strength of the lining layer is small, the fracture location due to bending will be different from the fracture location of the concrete base material. In other words, the concrete and the lining layer do not behave as one, indicating that the lining layer does not have sufficient followability when cracks occur in the concrete.
試験の結果からNo、2の試料、すなわちポリマール8
414とチョツプドストランドガラスマットの組み合わ
せが最もよいことが分った。From the test results, sample No. 2, i.e. Polymer 8
It was found that the combination of 414 and chopped strand glass mat was the best.
実施例3
石綿板(5mm厚)を切断した後、二つの切断面をつき
合わせ、この上に被覆処理を行った。硬化後、この試料
を用いて引張り試験を行い、ゼロスパン強度の推定を行
った。なお使用した樹脂の中、ポリマール6305は式
日薬品工業(抹)製の不飽和ポリエステル樹脂で、樹脂
硬化物の物性は、引張り強さ7.2kg/mm’、引張
り弾性率330 kg/++++++”。Example 3 After cutting an asbestos board (5 mm thick), the two cut surfaces were brought together and a coating was applied thereon. After curing, a tensile test was conducted using this sample to estimate the zero span strength. Among the resins used, Polymer 6305 is an unsaturated polyester resin manufactured by Shikinichi Yakuhin Kogyo Co., Ltd., and the physical properties of the cured resin are as follows: tensile strength 7.2 kg/mm', tensile modulus 330 kg/++++++ .
引張り伸び4.3%であった。The tensile elongation was 4.3%.
試験の結果を表−3に示す。試料の破断状況。The test results are shown in Table-3. Fracture condition of sample.
破断時の伸びなどからNo、 1 、 No、5 、す
なわちポリマール8414とチョツプドストランドガラ
スマットの組み合わせが最もよかった。In terms of elongation at break, No. 1, No. 5, ie, the combination of Polymer 8414 and chopped strand glass mat, were the best.
実施例4
屋外の地打ちコンクリート面に実施例1で用いたイソシ
アネート化合物Aを250g/m”の割合で刷毛塗りし
、3時間放置後、チョツプドストランドガラスマットを
1層、ポリエステル樹脂を用いてライニングした。樹脂
とガラスの割合は77:23(重量比)で、樹脂はポリ
マール8414とポリマール3276を用いて行った。Example 4 Isocyanate compound A used in Example 1 was applied with a brush to an outdoor cast concrete surface at a rate of 250 g/m'', and after being left for 3 hours, one layer of chopped strand glass mat and polyester resin were applied. The ratio of resin to glass was 77:23 (weight ratio), and Polymer 8414 and Polymer 3276 were used as the resins.
ライニングの面積は長さ10m、横巾0.3mである。The area of the lining is 10 m long and 0.3 m wide.
施工の際、マットの長さ方向の端を溝の縁に沿わせて直
角に折り曲げて施工し、他の端は平面のままで、収縮の
際ライニング層が動ける様にした。During installation, the lengthwise edge of the mat was bent at right angles along the edge of the groove, while the other edge remained flat to allow movement of the lining layer during shrinkage.
ここで用いたポリマール3276は式日薬品工業(株)
製の不飽和ポリエステル樹脂で、樹脂硬化物の物性は引
張り強さ6 、1 kg/n+m’、引張り弾性率30
0 kg/mm”、伸び率2.9%である。Polymer 3276 used here is manufactured by Shikinichi Yakuhin Kogyo Co., Ltd.
The physical properties of the cured resin are tensile strength 6.1 kg/n+m' and tensile modulus 30.
0 kg/mm” and elongation rate of 2.9%.
風雨にさらされたライニング面を観察した結果、弾性率
が大きくて、伸びの小さい3276を用いたライニング
層は、施工後9ケ月で平面の端から剥離を起こした。As a result of observing the lining surface exposed to wind and rain, the lining layer using 3276, which has a high elastic modulus and low elongation, peeled off from the edge of the flat surface 9 months after construction.
一方、8414の施工面は3年経過後も剥離などの異常
はない。On the other hand, there are no abnormalities such as peeling on the construction surface of 8414 even after three years.
(以 下 余 白)
表−2[曲げ試験によるライニング病のひび割わ、自浄
性]A・・・タケネート300C(固形分15%)S・
・・ポリマール8414
I]・・・ポリマール3517
M・・・チコップドストランドガラスマット(450g
/al′)
C・・・ガラスクロス目抜平織(300g/mつ最大荷
重時の相対たわみ量
(XIO−3mm)
最大荷重時以降約50Kgfに達した時の相対たわみ量
(Xl0−’ mm)
最終たわみ量からの計算値
イ・・・コンクリート破断箇所と同一
箇所でライニング層の破断
口・・ライニング層が剥離しコンクリートと別箇所で破
断(Margin below) Table 2 [Cracks due to lining disease and self-cleaning properties determined by bending test] A...Takenate 300C (solid content 15%) S.
... Polymer 8414 I] ... Polymer 3517 M ... Chikopdo strand glass mat (450g
/al') C...Glass cloth plain weave (300g/m) Relative deflection at maximum load (XIO-3mm) Relative deflection when approximately 50Kgf is reached after maximum load (X10-' mm) Calculated value from the final deflection A...The lining layer breaks at the same point as the concrete breakage point...The lining layer peels off and breaks at a different point from the concrete.
Claims (1)
以下であるイソシアネート化合物をプライマーとして塗
布し、つづいてチョップドストランドガラスマットと硬
化物の物性が引張り強さ0.5kg/mm^2以上、引
張り弾性率50kg/mm^2以下、引張り伸び30%
以上である不飽和ポリエステル樹脂を用いてライニング
層を作ることを特徴とするセメント系基材の被覆方法。Molecular weight per NCO group in cement base material is 200
The following isocyanate compound is applied as a primer, and the physical properties of the chopped strand glass mat and cured product are tensile strength of 0.5 kg/mm^2 or more, tensile modulus of 50 kg/mm^2 or less, and tensile elongation of 30%.
A method for coating a cement base material, characterized by forming a lining layer using the above unsaturated polyester resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62255869A JP2565723B2 (en) | 1987-10-08 | 1987-10-08 | Cement-based base material coating method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62255869A JP2565723B2 (en) | 1987-10-08 | 1987-10-08 | Cement-based base material coating method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0196079A true JPH0196079A (en) | 1989-04-14 |
| JP2565723B2 JP2565723B2 (en) | 1996-12-18 |
Family
ID=17284706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62255869A Expired - Fee Related JP2565723B2 (en) | 1987-10-08 | 1987-10-08 | Cement-based base material coating method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2565723B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6316089B1 (en) | 1997-12-05 | 2001-11-13 | Showa Denko K.K. | Photocurable prepreg sheet for waterproofing, method and apparatus for production of prepreg sheet, and waterproofing method using the sheet |
| KR100398275B1 (en) * | 1996-03-20 | 2003-12-24 | 삼성종합화학주식회사 | Resin Mortar Composition |
| JP2007245540A (en) * | 2006-03-16 | 2007-09-27 | Dainippon Ink & Chem Inc | Composite covering structure |
| JP2013151419A (en) * | 2006-12-13 | 2013-08-08 | James Hardie Technology Ltd | Engineered composite building material and method of making the same |
-
1987
- 1987-10-08 JP JP62255869A patent/JP2565723B2/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100398275B1 (en) * | 1996-03-20 | 2003-12-24 | 삼성종합화학주식회사 | Resin Mortar Composition |
| US6316089B1 (en) | 1997-12-05 | 2001-11-13 | Showa Denko K.K. | Photocurable prepreg sheet for waterproofing, method and apparatus for production of prepreg sheet, and waterproofing method using the sheet |
| JP2007245540A (en) * | 2006-03-16 | 2007-09-27 | Dainippon Ink & Chem Inc | Composite covering structure |
| JP2013151419A (en) * | 2006-12-13 | 2013-08-08 | James Hardie Technology Ltd | Engineered composite building material and method of making the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2565723B2 (en) | 1996-12-18 |
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