JPS632994B2 - - Google Patents
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- Publication number
- JPS632994B2 JPS632994B2 JP59118410A JP11841084A JPS632994B2 JP S632994 B2 JPS632994 B2 JP S632994B2 JP 59118410 A JP59118410 A JP 59118410A JP 11841084 A JP11841084 A JP 11841084A JP S632994 B2 JPS632994 B2 JP S632994B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- parts
- building material
- material composition
- composition according
- 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
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- 239000000203 mixture Substances 0.000 claims description 27
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000000839 emulsion Substances 0.000 claims description 12
- 238000010276 construction Methods 0.000 claims description 11
- 239000004566 building material Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 8
- 229920000570 polyether Polymers 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 239000000945 filler Substances 0.000 claims description 6
- 229920005862 polyol Polymers 0.000 claims description 6
- 150000003077 polyols Chemical class 0.000 claims description 6
- 229920003002 synthetic resin Polymers 0.000 claims description 6
- 239000000057 synthetic resin Substances 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 239000003292 glue Substances 0.000 claims description 3
- 239000005056 polyisocyanate Substances 0.000 claims description 3
- 229920001228 polyisocyanate Polymers 0.000 claims description 3
- 239000002893 slag Substances 0.000 claims description 3
- 229920001971 elastomer Polymers 0.000 claims description 2
- 239000000017 hydrogel Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 239000004033 plastic Substances 0.000 claims description 2
- 239000005060 rubber Substances 0.000 claims description 2
- 239000004568 cement Substances 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- 239000000499 gel Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 150000002009 diols Chemical class 0.000 description 6
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000004576 sand Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 description 4
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000009499 grossing Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 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 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- -1 hydrogen compound Chemical class 0.000 description 2
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 2
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 239000010451 perlite Substances 0.000 description 2
- 235000019362 perlite Nutrition 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000002023 wood Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- AREWWPRVYOZSFA-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;propane-1,2,3-triol Chemical compound OCC(O)CO.OCC(CO)(CO)CO AREWWPRVYOZSFA-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000003513 alkali Substances 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
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229920006184 cellulose methylcellulose Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000001031 chromium pigment Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- CYKDLUMZOVATFT-UHFFFAOYSA-N ethenyl acetate;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=O)OC=C CYKDLUMZOVATFT-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000011507 gypsum plaster Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 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
- 238000004898 kneading Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- FOWDZVNRQHPXDO-UHFFFAOYSA-N propyl hydrogen carbonate Chemical compound CCCOC(O)=O FOWDZVNRQHPXDO-UHFFFAOYSA-N 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Description
【発明の詳細な説明】
技術分野
本発明は、建築物の壁、天井、床等の化粧用上
塗材として左官工事または塗装工事に用いる建材
組成物に関する。DETAILED DESCRIPTION OF THE INVENTION Technical Field The present invention relates to a building material composition used for plastering or painting as a decorative top coating material for walls, ceilings, floors, etc. of buildings.
背景技術および解決課題
従来例えば左官工事に使用される化粧用上塗材
には、ケイ砂、雲母、パーライト、バーミキユラ
イト、炭酸カルシウム等の骨材に、無機および有
機の繊維、着色材それに接着用糊料等を配合した
混合物が使用されており、これらは使用時水また
は合成樹脂エマルジヨンを添加して混練し、コテ
塗り、吹き付け等により施工されていた。ところ
がこれら上塗材の硬化は水分の自然蒸発によるも
のであり、塗面が十分に硬化するに至らないにし
ても十分に安定な状態、すなわち電気、ガス工事
等次の工程に取りかゝることができるまでには通
常数日を要し、特に冬期や雨期にはその期間が長
くなり、トータルの工事日数がそれだけ延長す
る。BACKGROUND TECHNOLOGY AND PROBLEMS TO BE SOLVED Traditionally, for example, decorative topcoating materials used in plastering work include aggregates such as silica sand, mica, perlite, vermiculite, and calcium carbonate, inorganic and organic fibers, colorants, and adhesives. Mixtures containing glue and the like are used, and when used, these are kneaded with water or synthetic resin emulsion, and applied by troweling, spraying, etc. However, the curing of these top coat materials is due to natural evaporation of water, so even if the coated surface is not fully cured, it is still in a sufficiently stable state, which means that it is possible to proceed to the next process such as electrical or gas work. It usually takes several days to complete the construction, and this period is particularly long during the winter and rainy seasons, extending the total number of construction days accordingly.
また塗装面が軟らかい状態になる乾燥硬化前
に、誤つて人や物体が接触して塗面を傷付けるこ
とがあり、また水に触れるとその部分が洗い流さ
れ、補修や再施工を必要とする。 Furthermore, before the painted surface dries and hardens, when it becomes soft, people or objects may accidentally come into contact with the painted surface and damage it, and if it comes into contact with water, the affected area will be washed away, requiring repair or repainting.
本発明は、壁、天井、床等の左官工事用または
塗装工事用の水性上塗材の施工後、数時間以内に
弾力性ある含水ゲルを不可逆的に生成し、従つて
完全に硬化する以前に物体が触れても付着せず、
物体によつて変形しても弾性によつて元の状態へ
復帰し、塗面が傷付かない安定状態に達し、次の
工事を数時間以内に開始することが可能な上塗用
建材組成物を提供することを課題とする。 The present invention irreversibly produces an elastic water-containing gel within a few hours after application of water-based topcoats for plastering or painting of walls, ceilings, floors, etc., and therefore before completely curing. Even if an object touches it, it will not stick to it,
We have created a building material composition for top coating that returns to its original state due to its elasticity even if it is deformed by an object, reaches a stable state where the painted surface is not damaged, and allows the next construction work to be started within a few hours. The challenge is to provide.
解決法
本発明の課題は、公知の水性上塗材へ親水性ウ
レタンプレポリマーを添加することによつて解決
される。Solution The object of the invention is solved by adding a hydrophilic urethane prepolymer to known aqueous topcoats.
すなわち、本発明は充填材およびその結合材を
必須成分として含み、かつ親水性ウレタンプレポ
リマーを含有することを特徴とする前記水性上塗
用建材組成物を提供する。 That is, the present invention provides the aqueous top-coat building material composition, which contains a filler and its binder as essential components and also contains a hydrophilic urethane prepolymer.
詳細な議論
本発明に用いる親水性ウレタンプレポリマー
は、水に溶解または分散するウレタンプレポリマ
ーである。周知のようにウレタンプレポリマー
は、分子末端に未反応遊離イソシアネート基を有
し、活性水素化合物と反応して鎖延長および/ま
たは架橋してポリウレタンをつくる。水の活性水
素化合物の一種であり、前記遊離イソシアネート
基と反応して尿素結合を形成して鎖延長および/
または架橋する。その際ウレタンプレポリマー自
体が水中に溶解または均一に分散していると、前
記のように一部の水と反応して鎖延長および/ま
たは架橋すると同時に、系内の水をポリウレタン
のマトリツクス内に取り込み、弾力性ある含水ゲ
ルを生成する。一旦生成した含水ゲルは化学的お
よび物理的に安定であり、かなりの機械的シヨツ
クによつても破壊されない。従つてこの親水性ウ
レタンプレポリマーを前記上塗用建材組成物へ添
加し、常法により水と混練して施工した場合、少
なくとも数時間以内に塗面がゲル化し、次の工事
を再開しても支障のない安定状態となる。Detailed Discussion The hydrophilic urethane prepolymers used in the present invention are urethane prepolymers that dissolve or disperse in water. As is well known, urethane prepolymers have unreacted free isocyanate groups at the molecular ends, and react with active hydrogen compounds to extend the chain and/or crosslink to form polyurethanes. A type of active hydrogen compound in water, which reacts with the free isocyanate group to form a urea bond, resulting in chain extension and/or
or crosslink. At this time, if the urethane prepolymer itself is dissolved or uniformly dispersed in water, it will react with some of the water to cause chain extension and/or crosslinking as described above, and at the same time, the water in the system will be transferred into the polyurethane matrix. Incorporated into an elastic water-containing gel. Once formed, the hydrogel is chemically and physically stable and is not destroyed by even significant mechanical shock. Therefore, when this hydrophilic urethane prepolymer is added to the above-mentioned construction material composition for top coating and kneaded with water for construction, the painted surface gels within at least a few hours, and even if the next construction is restarted, there is no problem. It will be in a stable state without any problems.
このような親水性ポリウレタンは、ポリイソシ
アネート化合物とポリエーテルポリオールとを、
前者を後者に対して過剰に、すなわちNCO/OH
の比が少なくとも2以上になるように常法によつ
て反応させることによつて得られる。ポリイソシ
アネート化合物としては、トリレンジイソシアネ
ート、キシリレンジイソシアネート、4・4′−ジ
フエニルメタンジイソシアネート、ヘキサメチレ
ンジイソシアネート、イソホロンジイソシアネー
ト、添水4・4′−ジフエニルメタンジイソシアネ
ート等が用いられる。ポリエーテルポリオールと
しては、出発物質として二価のアルコール、例え
ばエチレングリコールを用い、これにエチレンオ
キサイド単独または他のアルキレンオキサイドを
ランダムもしくはブロツク共重合体の形に付加し
て得られるポリエーテルジオールが用いられる。
二価のアルコールの代わりに三価以上のアルコー
ル、例えばグリセリンペンタエリスリトール、ソ
ルビトール等を出発物質として用いて得られるホ
リエーテルポリオールも単独またはポリエーテル
ジオールと併用して用いることができる。 Such hydrophilic polyurethane is made by combining a polyisocyanate compound and a polyether polyol.
Excess of the former relative to the latter, i.e. NCO/OH
It can be obtained by reacting in a conventional manner such that the ratio of the two is at least 2 or more. As the polyisocyanate compound, tolylene diisocyanate, xylylene diisocyanate, 4,4'-diphenylmethane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, water-added 4,4'-diphenylmethane diisocyanate, etc. are used. As the polyether polyol, a polyether diol obtained by using a dihydric alcohol such as ethylene glycol as a starting material and adding ethylene oxide alone or other alkylene oxide to this in the form of a random or block copolymer is used. It will be done.
Polyether polyols obtained by using trihydric or higher alcohols such as glycerin pentaerythritol, sorbitol, etc. as starting materials instead of dihydric alcohols can also be used alone or in combination with polyether diols.
ウレタンプレポリマーが水溶性または水分散性
であるためには、親水性ブロツクであるエチレン
オキシド単位が全アルキレンオキシド含量に対し
少なくとも20%でなければならない。またポリエ
ーテルポリオールが過度に親水性であると最終塗
膜の耐水性が低下するので、適当な割合で疏水性
ブロツクを含むのが好ましい。また同様な理由
で、ポリエーテルポリオールの分子量は、OH1
個当たり400〜4000であることが好ましい。水分
散性、皮膜形成性および作業性等から考えて、エ
チレンオキシドとプロピレンオキシドの重量比が
20:80〜90:10の範囲にある、分子量800〜8000
のポリオキシエチレンポリオキシプロピレングリ
コールが特に好ましい。 In order for a urethane prepolymer to be water-soluble or water-dispersible, the hydrophilic block ethylene oxide units must account for at least 20% of the total alkylene oxide content. Furthermore, if the polyether polyol is excessively hydrophilic, the water resistance of the final coating film will be reduced, so it is preferable to contain a hydrophobic block in an appropriate proportion. For the same reason, the molecular weight of polyether polyol is OH1
The number is preferably 400 to 4000 per piece. Considering water dispersibility, film forming properties, workability, etc., the weight ratio of ethylene oxide and propylene oxide is
Molecular weight 800-8000 in the range 20:80-90:10
Particularly preferred are polyoxyethylene polyoxypropylene glycols.
親水性ウレタンプレポリマーは、そのまゝまた
はアセトン、メチルエチルケトン、プロピルカー
ボネート等イソシアネート基と反応しない溶剤で
希釈し、残余の成分とは別個の容器に貯蔵し、使
用時現場で混合して水で混練して施工するのが好
ましい。 The hydrophilic urethane prepolymer can be used as is or diluted with a solvent that does not react with isocyanate groups, such as acetone, methyl ethyl ketone, or propyl carbonate, stored in a separate container from the rest of the ingredients, and mixed on site before use and kneaded with water. It is preferable to carry out construction.
充填材とは骨材を含む意味であり、パーライ
ト、パーミキユライト、陶粉、炭酸カルシウム、
クレー、ベントナイト、アルミナ、雲母、寒水
石、ケイ砂、ケイソウ土、鉱滓等がある。 Filler includes aggregate, such as perlite, permiculite, ceramic powder, calcium carbonate,
These include clay, bentonite, alumina, mica, anhydrite, silica sand, diatomaceous earth, and slag.
化粧用壁材には、充填材として無機または有機
の繊維や粉砕物を使用することができる。これら
は、粉砕バルブ、人絹粉、綿粉、人絹糸、綿糸、
毛糸、合成繊維、石綿、岩綿、グラスウール、セ
ロハン、ゴム、プラスチツク、木材の粉砕物等が
ある。また色材として、前記材料の着色されたも
のや、金属粉、顔料または染料を含んでもよい。 For decorative wall materials, inorganic or organic fibers or pulverized materials can be used as fillers. These are crushed valve, human silk powder, cotton powder, human silk thread, cotton thread,
Examples include wool, synthetic fibers, asbestos, rock wool, glass wool, cellophane, rubber, plastic, and crushed wood. The coloring material may also include colored versions of the above materials, metal powder, pigments, or dyes.
結合材とは粘度調整剤を含む趣旨であり、一般
に水溶性の糊料である。CMC、ヒドロキシメチ
ルセルロース、メチルセルロース、水分散性粉末
樹脂、合成樹脂エマルジヨン等が用いられる。 The binder includes a viscosity modifier and is generally a water-soluble glue. CMC, hydroxymethylcellulose, methylcellulose, water-dispersible powder resin, synthetic resin emulsion, etc. are used.
その他従来公知の水性上塗用建材組成物に用い
られている成分はすべて使用することができ、そ
れらの種類、配合割合等も使用目的に応じて常法
により任意に調節し得る。 All other components conventionally used in aqueous top-coat building material compositions can be used, and their types, blending ratios, etc. can be arbitrarily adjusted according to the purpose of use by conventional methods.
本発明による親水性ウレタンプレポリマーの使
用量は、混練に用いる水(合成樹脂エマルジヨン
中の水をも含む)の量に依存する。すなわち水量
100部当たりウレタンプレポリマーとして少なく
とも5重量部使用することが好ましく、上限は主
として経済的理由によつて決められる。 The amount of hydrophilic urethane prepolymer used according to the invention depends on the amount of water (including water in the synthetic resin emulsion) used for kneading. i.e. water volume
It is preferred to use at least 5 parts by weight of urethane prepolymer per 100 parts, the upper limit being determined primarily by economic considerations.
施工に際しては、親水性ウレタンプレポリマー
を余分に添加することを除いて常法に従うことが
できる。すなわち、ウレタンプレポリマーと、水
と、残余の成分とをよく混練し、こて、スプレー
ガン、ローラー等により施工面に上塗りし、自然
に硬化、乾燥するのを待てばよい。その際施工後
少なくとも数時間以内に塗面がゲル化して安定
し、塗面に触れることもできる。またこの状態に
至るまでの所要時間、および作業可能時間を調節
するため、場合により、酸等の遅延剤、またはア
ルカリ等の促進剤を用いることができる。 At the time of construction, conventional methods can be followed except for adding extra hydrophilic urethane prepolymer. That is, the urethane prepolymer, water, and the remaining components are thoroughly kneaded, the top coat is applied to the construction surface using a trowel, a spray gun, a roller, etc., and the mixture is allowed to naturally harden and dry. At this time, the painted surface gels and becomes stable within at least a few hours after application, and the painted surface can even be touched. Further, in order to adjust the time required to reach this state and the workable time, a retardant such as an acid or an accelerator such as an alkali may be used as the case requires.
最終的に得られる塗膜は、ウレタンプレポリマ
ーを含まない従来の上塗材に比較して弾性に富
み、硬度、耐水性にもすぐれている。また下地と
の接着性も良好である。 The final coating film has greater elasticity, hardness, and water resistance than conventional top coating materials that do not contain urethane prepolymers. It also has good adhesion to the base.
以下に本発明の実施例を示す。実施例中部およ
び%は重量による。 Examples of the present invention are shown below. Examples and percentages are by weight.
親水性ウレタンプレポリマーの製造
製造例 1
エチレングリコールにエチレンオキサイドを常
法で付加重合させて平均分子量2000のジオールを
得た。このジオール792重量部とトリレンジイソ
シアネート(2・4−;2・6−異性体比80:
20)208重量部とを窒素気流中で90℃、3時間反
応させてプレポリマーを得た。Production Example of Hydrophilic Urethane Prepolymer 1 Ethylene oxide was addition-polymerized to ethylene glycol in a conventional manner to obtain a diol having an average molecular weight of 2000. 792 parts by weight of this diol and tolylene diisocyanate (2.4-; 2.6-isomer ratio 80:
20) 208 parts by weight were reacted at 90°C in a nitrogen stream for 3 hours to obtain a prepolymer.
これは水に均一に分散し、5%以上の濃度では
弾性のある抱水ゲル体を作る。 It is uniformly dispersed in water and forms an elastic hydrated gel at a concentration of 5% or more.
製造例 2
ジエチレングリコールにエチレンオキサイドと
プロピレンオキサイドをブロツク状で常法で付加
重合させて平均分子量3000のジオールを得た。こ
の時のエチレンオキサイドとプロピレンオキサイ
ドの重量比は、80:20である。得られたジオール
800重量部とメタキシリレンジイソシアネート200
重量部とを窒素気流中で90℃、4時間反応させて
プレポリマーを得た。Production Example 2 A diol having an average molecular weight of 3000 was obtained by addition polymerizing ethylene oxide and propylene oxide to diethylene glycol in the form of a block using a conventional method. The weight ratio of ethylene oxide and propylene oxide at this time was 80:20. Diol obtained
800 parts by weight and 200 parts metaxylylene diisocyanate
Parts by weight were reacted at 90° C. for 4 hours in a nitrogen stream to obtain a prepolymer.
これは水に均一に分散し、10%以上の濃度では
弾性のある抱水ゲル体を作る。 It disperses uniformly in water and forms an elastic hydrated gel at concentrations above 10%.
製造例 3
トリメチロールプロパンにエチレンオキサイド
とプロピレンオキサイドをランダムで常法で付加
重合させて平均分子量4000のトリオールを得た。
この時のエチレンオキサイドとプロピレンオキサ
イドの重量比は90:10である。このトリオール
827重量部とヘキサメチレンジイソシアネート173
重量部とを窒素気流中で70℃、6時間反応させて
プレポリマーを得た。Production Example 3 Ethylene oxide and propylene oxide were randomly added to trimethylolpropane in a conventional manner to obtain a triol having an average molecular weight of 4000.
The weight ratio of ethylene oxide and propylene oxide at this time was 90:10. This triol
827 parts by weight and 173 parts by weight of hexamethylene diisocyanate
Parts by weight were reacted at 70° C. for 6 hours in a nitrogen stream to obtain a prepolymer.
これは水に均一に溶解し、10%以上の濃度では
抱水ゲル体を作る。 It dissolves uniformly in water and forms a hydrated gel at concentrations of 10% or more.
組成物および施工
実施例 1
組 成
パルプ粉砕物 100部
青色に着色された木粉 65部
黒色に染色されたセロハン切断片 5部
カルボキシメチルセルロースソーダ塩 20部
予め混合されたプレポリマー水溶液 1500部
(プレポリマー水溶液:水 1300部
:プレポリマー
200部)
これらの物を良く混合したのち、コテによつて
石膏プラスター中塗り壁面にムラなく塗装し、5
時間経過したところ、この塗装面を指で押しても
塗面の移動が無い優れた初期強度を有する淡い青
色の中に黒色斑を散りばめた美しい塗装面を得
た。また同組成物のうちプレポリマーを使用せ
ず、水のみで混練した同時施工壁面は24時間経過
しても、指で押さえると塗面の移動のある部分が
残り、プレポリマーを用いることにより5倍以上
の速さで初期強度を得ることが出来た。更にプレ
ポリマーを用いた壁面は接着強度が優れ、また水
をかけても流れない耐水性のある壁面が得られ
た。Composition and construction examples 1 Composition Pulverized pulp 100 parts Wood flour colored blue 65 parts Cellophane cut pieces dyed black 5 parts Carboxymethyl cellulose soda salt 20 parts Pre-mixed prepolymer aqueous solution 1500 parts Polymer aqueous solution: 1300 parts of water: Prepolymer
200 copies) After mixing these ingredients well, use a trowel to apply the gypsum plaster on the wall surface evenly, and apply 5 coats.
After a period of time, a beautiful painted surface with black spots scattered in a pale blue color was obtained, which had excellent initial strength and did not move even when pressed with a finger. In addition, even after 24 hours had elapsed on walls that were simultaneously applied using the same composition and kneaded with only water without using a prepolymer, there remained areas where the painted surface moved when pressed with a finger. We were able to obtain initial strength more than twice as quickly. Furthermore, the wall surface using the prepolymer has excellent adhesive strength, and a water-resistant wall surface that does not wash away even when water is poured on it was obtained.
実施例 2
組 成
聚楽色に着色された珪砂(20−100メツシユ)
100部
カルボキシメチルセルロースソーダ塩 1部
水 30部プレポリマー 15部
これらの組成物を良く混合したのち、コテによ
り、平坦なモルタル面に塗装し、2時間経過した
ところ実施例1に述べた通りの性能を有する聚楽
色の美しい砂壁を得た。Example 2 Composition Juraku colored silica sand (20-100 mesh)
100 parts carboxymethylcellulose soda salt 1 part water 30 parts prepolymer 15 parts These compositions were mixed well and applied to a flat mortar surface using a trowel. After 2 hours, the performance as described in Example 1 was observed. We obtained a beautiful sand wall in the color of Juraku.
実施例 3
組 成
20−60メツシユの寒水石 100部
18−48メツシユの黒色鉱滓粉砕物 10部
メチルセルロース 2部
水 20部プレポリマー 20部
これらの組成物を良く混合したのち、モルタル
床面に流し、コテによつて平滑にならして、4時
間経過したところ、弾性のあるみかげ石状の硬化
塗面を得、その上を軽く歩いても塗面を傷付ける
ことが無く次の塗装作業を進めることができた。Example 3 Composition: 100 parts of agarstone of 20-60 mesh. 10 parts of crushed black slag of 18-48 mesh. After 4 hours of smoothing with a trowel, an elastic, granite-like hardened paint surface was obtained, and the paint surface was not damaged even when lightly walked on, allowing the next painting process to proceed. was completed.
実施例 4
組 成
12−32メツシユ粒状岩綿 30部
60−200メツシユ粉砕綿 5部
クレー 65部
酸化チタン 1部
鉄 黄 0.1部
ポリビニールアルコール 1部
カルボキシメチルセルロース 2部
水 150部プレポリマー 30部
これらの物を良く混合したのち、コンクリート
天井面にリシンガンにより吹き付けし、2時間経
過したところ、指で触れても塗面の移動の無い初
期強度の優れた塗面が得られた。更に24時間経過
したところ、接着性および耐水性に優れた美しい
白の凹凸のある天井面を得た。Example 4 Composition 12-32 mesh granular rock wool 30 parts 60-200 mesh pulverized cotton 5 parts clay 65 parts titanium oxide 1 part iron yellow 0.1 part polyvinyl alcohol 1 part carboxymethylcellulose 2 parts water 150 parts prepolymer 30 parts these After mixing the mixture well, it was sprayed onto the concrete ceiling surface using a ricing gun, and after 2 hours, a coated surface with excellent initial strength was obtained that did not move even when touched with a finger. After another 24 hours, a beautiful white uneven ceiling surface with excellent adhesiveness and water resistance was obtained.
実施例 5
組 成
5m/mに切断された白色毛糸 30部
5m/mに切断されたビニロン甘ヨリ(褐色)
70部
カルボキシメチルセルロースソーダ塩 20部
水 400部プレポリマー 800部
これらの物を良く混合したのち、上壁面にコテ
により塗装し、6時間経過したところ、指で触れ
ても、塗面の移動の無い初期強度の優れた美しい
らくだ色に白色のにじんだ綿壁を得た。Example 5 Composition White wool yarn cut to 5 m/m 30 parts Vinylon Amagori (brown) cut to 5 m/m
70 parts carboxymethyl cellulose soda salt 20 parts water 400 parts prepolymer 800 parts After mixing these ingredients well, I painted the upper wall with a trowel.After 6 hours, there was no movement of the painted surface even when I touched it with my finger. A beautiful camel-colored and white cotton wall with excellent initial strength was obtained.
実施例 6
組 成
32−100メツシユ 50部
粉末重質炭酸カルシウム 40部
粉末軽質炭酸カルシウム 20部
酸化チタン 10部
水に分散したフタロシアニンブルー 0.1部
顔料分散剤 0.1部
ヒドロキシメチルセルロース 1部水 50部
上記の組成物をミキサーにより良く混合して塗
料化物とする。Example 6 Composition 32-100 mesh 50 parts heavy calcium carbonate powder 40 parts light calcium carbonate powder 20 parts titanium oxide 10 parts phthalocyanine blue dispersed in water 0.1 part pigment dispersant 0.1 part hydroxymethyl cellulose 1 part water 50 parts above The composition is thoroughly mixed with a mixer to form a paint.
この塗料化物100部にプレポリマー120部を加え
て良く混ぜたのち、ローラ刷毛によりモルタル壁
面に塗装し1時間経過したところ、指で触れても
塗面の移動が無く水をかけても流れない、美しい
白色のリシン状塗装面を得た。 After adding 120 parts of prepolymer to 100 parts of this paint compound and mixing well, I painted it on the mortar wall surface with a roller brush and after 1 hour, there was no movement of the painted surface when I touched it with my finger, and it did not wash away even when I poured water on it. A beautiful white ricin-like painted surface was obtained.
実施例 7
組 成
白色ポルトランドセメント 100部
48−200メツシユ珪砂 150部
絶色クロム顔料 10部
可溶性でんぷん 0.5部
水 30部プレポリマー 30部
上記の組成物を良く混合したのち、コンクリー
ト床面に流し、コテにより平滑にならして3時間
経過したところ、弾性のある緑色の硬化床面を
得、その上を軽く歩いても塗面を傷付けることが
無く次の塗装作業を行うことができた。Example 7 Composition White Portland cement 100 parts 48-200 mesh silica sand 150 parts colorless chromium pigment 10 parts Soluble starch 0.5 parts Water 30 parts Prepolymer 30 parts After the above composition was mixed well, it was poured onto a concrete floor surface and troweled. After 3 hours of smoothing and smoothing, an elastic green hardened floor surface was obtained, and the next painting work could be carried out without damaging the painted surface even when walking lightly on it.
実施例1〜7までの組成に合成樹脂エマルジヨ
ンを必要に応じて加えても良い。 A synthetic resin emulsion may be added to the compositions of Examples 1 to 7 as necessary.
合成樹脂エマルジヨンとは、酢酸ビニル樹脂エ
マルジヨン、エチレン−酢酸ビニル樹脂エマルジ
ヨン、合成ゴムエマルジヨン、酢ビ−アクリル酸
エステル共重合樹脂エマルジヨン、スチレン−ア
クリル酸エステル共重合樹脂エマルジヨン、アク
リル酸エステル共重合樹脂エマルジヨンなどであ
る。 Synthetic resin emulsions include vinyl acetate resin emulsion, ethylene-vinyl acetate resin emulsion, synthetic rubber emulsion, vinyl acetate-acrylic acid ester copolymer resin emulsion, styrene-acrylic acid ester copolymer resin emulsion, acrylic acid ester copolymer resin emulsion, etc. It is.
効 果
(i) 初期強度の発現時間が速く、電気、ガス等の
工事による塗面の傷付けがない。Effects (i) The initial strength is developed quickly, and the painted surface is not damaged by electricity, gas, etc. construction work.
(ii) 初期強度の発現が見られた時点で水をかけて
も、塗面が流れず、耐水性のある塗面が得られ
る。(ii) Even if water is applied once initial strength has been developed, the coated surface will not run off and a water-resistant coated surface can be obtained.
(iii) 硬化時間のコントロールが可能である。(iii) Curing time can be controlled.
(iv) 硬い皮膜や弾性のある皮膜など、皮膜物性の
コントロールが可能である。(iv) It is possible to control the physical properties of the film, such as hard or elastic films.
Claims (1)
み、かつエチレンオキシド単位を全アルキレンオ
キシド含量に対し少なくとも20重量%含んでいる
ポリエーテルポリオール成分とそれに対する当量
より過剰のポリイソシアネート化合物とを反応さ
せて得られる、水の存在下不可逆的に含水ゲルを
形成する水溶性または水分散性ウレタンプレポリ
マーを含有し、使用時水を加えて混練して左官工
事または塗装工事に上塗材として用いることを特
徴とする水性建材組成物。 2 充填材が無機または有機繊維質材料である第
1項の建材組成物。 3 充填材が、鉱物、鉱滓、セメント、金属粉等
の無機粉砕物またはゴム、プラスチツク、木材等
の有機粉砕物である第1項の建材組成物。 4 結合材が糊料および/または合成樹脂エマル
ジヨンである第1項ないし第3項のいずれかの建
材組成物。 5 ウレタンプレポリマーと残余の成分とは使用
前別々の容器に貯えられ、使用時に現場で混和し
て水で混練して施工される第1項ないし第4項の
いずれかの建材組成物。[Scope of Claims] 1. A polyether polyol component containing a filler and its binder as an essential component and containing at least 20% by weight of ethylene oxide units based on the total alkylene oxide content, and a polyisocyanate compound in excess of the equivalent amount thereof. Contains a water-soluble or water-dispersible urethane prepolymer that irreversibly forms a hydrogel in the presence of water, obtained by reacting with An aqueous building material composition characterized in that it is used as a water-based building material composition. 2. The building material composition according to item 1, wherein the filler is an inorganic or organic fibrous material. 3. The building material composition according to item 1, wherein the filler is an inorganic pulverized material such as minerals, slag, cement, metal powder, etc. or an organic pulverized material such as rubber, plastic, wood, etc. 4. The building material composition according to any one of Items 1 to 3, wherein the binder is a glue and/or a synthetic resin emulsion. 5. The building material composition according to any one of Items 1 to 4, wherein the urethane prepolymer and the remaining components are stored in separate containers before use, and upon use, are mixed on site and kneaded with water for construction.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11841084A JPS60262872A (en) | 1984-06-08 | 1984-06-08 | Building material composition for overcoating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11841084A JPS60262872A (en) | 1984-06-08 | 1984-06-08 | Building material composition for overcoating |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60262872A JPS60262872A (en) | 1985-12-26 |
JPS632994B2 true JPS632994B2 (en) | 1988-01-21 |
Family
ID=14735952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11841084A Granted JPS60262872A (en) | 1984-06-08 | 1984-06-08 | Building material composition for overcoating |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60262872A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001049163A (en) * | 1999-08-04 | 2001-02-20 | Wolff Walsrode Ag | Coating agent containing cellulosic material and its use in lacquer |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5141646A (en) * | 1974-10-05 | 1976-04-08 | Kubota Ltd | Chukohinno hyomenshorihoho |
-
1984
- 1984-06-08 JP JP11841084A patent/JPS60262872A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5141646A (en) * | 1974-10-05 | 1976-04-08 | Kubota Ltd | Chukohinno hyomenshorihoho |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001049163A (en) * | 1999-08-04 | 2001-02-20 | Wolff Walsrode Ag | Coating agent containing cellulosic material and its use in lacquer |
Also Published As
Publication number | Publication date |
---|---|
JPS60262872A (en) | 1985-12-26 |
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