JPH0448510B2 - - Google Patents
Info
- Publication number
- JPH0448510B2 JPH0448510B2 JP62147535A JP14753587A JPH0448510B2 JP H0448510 B2 JPH0448510 B2 JP H0448510B2 JP 62147535 A JP62147535 A JP 62147535A JP 14753587 A JP14753587 A JP 14753587A JP H0448510 B2 JPH0448510 B2 JP H0448510B2
- Authority
- JP
- Japan
- Prior art keywords
- floor
- floor surface
- polymer
- molecular weight
- coating film
- 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
- 238000000576 coating method Methods 0.000 claims description 20
- 239000011248 coating agent Substances 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 238000004140 cleaning Methods 0.000 claims description 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 7
- 230000003749 cleanliness Effects 0.000 claims description 5
- 239000002344 surface layer Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000012459 cleaning agent Substances 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 238000005498 polishing Methods 0.000 description 19
- 239000001993 wax Substances 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 238000009408 flooring Methods 0.000 description 5
- 238000012423 maintenance Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 239000012986 chain transfer agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- -1 etc.) Chemical compound 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000010865 sewage Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 239000003021 water soluble solvent Substances 0.000 description 2
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- DYBIGIADVHIODH-UHFFFAOYSA-N 2-nonylphenol;oxirane Chemical compound C1CO1.CCCCCCCCCC1=CC=CC=C1O DYBIGIADVHIODH-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 101100172132 Mus musculus Eif3a gene Proteins 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- XNNQFQFUQLJSQT-UHFFFAOYSA-N bromo(trichloro)methane Chemical compound ClC(Cl)(Cl)Br XNNQFQFUQLJSQT-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000004018 waxing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
Description
−産業上の利用分野−
本発明は建築物の床面、特にプラスチツク系の
床材の表面を清浄で光沢のある表面に維持するた
めのメンテナンス方法に関するものである。
−従来の技術−
建築物の床面に光沢と清浄さを付与するために
艷出し剤を塗布することは、従来より行われてい
る。床材がプラスチツク系の床材である場合に
は、艷出し剤としてノンバフアブルタイプ又はセ
ミバフアブルタイプと呼ばれる樹脂系ワツクスが
用いられる。このようなワツクスを塗布した床面
は、その表面が樹脂ワツクスにより保護されて光
沢性及び耐汚損性を備えるが、使用による光沢の
減退、ブラツクヒールマーク等による汚損、表面
の瑕付き等は避けられない。そこで定期的に表面
を洗浄して清浄と光沢を維持する作業、即ちメン
テナンス作業が必要となる。
樹脂系ワツクスを塗布した床面の従来のメンテ
ナンス作業は、床面のゴミを除去し、洗浄剤
で汚れを落とし、洗浄により生じた汚水を除い
て乾燥させ、再度樹脂系ワツクスを塗布して仕
上げる、という手順で行われている。
−発明が解決しようとする問題点−
しかし上記,の洗浄工程は、多量の水を使
用するため、床面に設置された器物を移し変えて
行わねばならず又汚水吸入装置等の機器を用いね
ばならないため作業が煩雑であり、更に床面に隙
間等があると汚水が床下に漏れる問題がある。
而も上記洗浄工程で用いられている従来の洗浄
剤では、床の表層面に固着しあるいはその表層面
から内部にまで食い込んだ汚れを単純な拭き取り
乃至洗い落とし作業で除去することは困難である
という問題がある。例えばビニールタイルやビニ
ールアスベストタイルは、事務所や病院等の床材
として広く使用され、通常この床材の上に樹脂系
ワツクスが塗布されているが、この上をゴム底の
靴で歩行すると靴底の擦跡(ブラツクヒールマー
ク)がワツクス皮膜の内部に食い込んで黒く残
る。この汚れを通常の洗浄剤で洗い落す事は困難
であり、この場合には「剥離剤」と呼ばれるセロ
ソルブ類等を混入した洗浄剤で樹脂系ワツクスと
共に剥離するという作業が必要であり、きわめて
煩雑である。
一方、樹脂系ワツクスに洗剤として作用するア
ルカリ可溶性樹脂と界面活性剤を付加することに
より、ワツクスがけと同時に古い被膜の洗浄も行
うツヤ出し剤は公知である。しかしながらこの種
のツヤ出し剤は、油汚れ等の被膜表面の軽微な汚
れを除去することはできるが、ブラツクヒールマ
ークのようにコーテイング被膜に食い込んだ汚れ
を落とすことは到底不可能である。また、多量の
アルカリ可溶性樹脂の付加は、再形成されるコー
テイング被膜の保護被膜としての機能、特に耐水
性を大きく低下させる欠点がある。
この発明は、従来の上記問題点を解決すること
を目的とするもので、従来のような洗浄剤や剥離
剤を用いる洗浄工程を必要とせず、従来の上記
乃至の工程を一工程で行うことができ、従つて
床面の清浄維持作業がきわめて容易にでき、而も
床面を光沢に優れ且つ強靭な耐水性、耐久性およ
び耐汚損性を有するコーテイング被膜で保護する
ことができる床面の清浄維持方法を提供すること
を目的としている。
−問題点を解決するための手段−
本発明の方法では、床面の清浄を維持するため
のツヤ出し洗浄剤が用いられる。このツヤ出し洗
浄剤は、重量平均分子量が8000を越え45000以下
の下記構造式を有する重合体を重量パーセントで
6ないし24パーセント含み、PH6.5ないし10の水
溶液となした組成物である。
上記構造式中Mは必要により付加共重合する他
のビニールモノマー、R1は水素または炭素数1
ないし3個を有するアルキル基、R2は炭素数1
ないし8個のアルキル基および酸価を重合体1グ
ラム当り70ないし650mgKOHにするに必要な水
素、m,nは前記重合体の重量平均分子量を8000
を越え45000以下とするに必要な正数を表わす。
この発明の方法では、上記組成物からなるツヤ
出し洗浄剤を予め樹脂系ワツクスを塗布し又は塗
布しない床面に塗布して乾燥させ、該床面の表層
面にこのツヤ出し洗浄剤が乾燥することによつて
形成されるコーテイング被膜を形成する。そして
床面が汚損されたときには、上記ツヤ出し洗浄剤
を含ませたモツプ等で該床面を拭くことにより、
古い被膜を再溶解させて汚れを除去すると共にそ
の表層面に当該ツヤ出し洗浄剤の新たなコーテイ
ング被膜を形成している。
このツヤ出し洗浄剤に含まれる重合体の単量体
は、ランダムに結合されている。該単量体は、例
えばメタクリル酸メチルエステル、アクリル酸ブ
チルエステル、メタクリル酸、アクリル酸等であ
り、必要によりアクリロニトリル、酢酸ビニー
ル、スチレン等のビニールモノマーを共重合体と
して使用できる。また、酸価はアクリル酸または
メタクリル酸の量により調整する。
上記単量体の重合は、常法の溶液重合法、塊状
重合法、懸濁重合法、乳化重合法により行われ
る。分子量を調整するには連鎖移動剤を用いるの
も効果的である。連鎖移動剤としてはメルカプタ
ン類、ハロゲン化炭素類が使用でき、具体的には
ドデシルメルカプタン、ラウリルメルカプタン、
四塩化炭素、ブロモトリクロロメタン等である。
重合体の分子量は重合条件によつても異なるが連
鎖移動剤と重量体のモル比で大体決定づけられ、
具体例として米国特許2870116号、米国特許
2870117号、特公昭47−14019号等に例示されてい
る。分子量の調整の別の方法としては、重合温
度、重合開始剤の濃度、溶液重合の溶剤の種類に
よつても調整され、特開昭54−64532号に例示さ
れている。こうして得られた重合体が多量の連鎖
移動剤を含んで異臭を有したり、溶剤類の混入、
残留モノマー臭の問題等が発生する場合、これ等
を除去する必要があり、このような時には、水と
の共沸除去或いは水蒸気蒸留除去、減圧蒸留除去
等によりこれ等のほぼ完全な除去が可能である。
こうして得られた重合体の分子量は、ゲルパミユ
ーシヨンクロマトグラフイー(GPC法)により
容易に測定できる。
上記により得られた重合体は、カルボキシル基
がアンモニウム或いはアミン、アミノアルコール
類で中和し塩となり水溶性を呈し水に溶解し、外
観は淡黄又は無色の透明又は半透明を呈する。
−作用−
上記重合体の水溶液、即ち本発明でいうところ
のツヤ出し洗浄剤を床面に塗布すると、揮発分が
乾燥除去され、充分な耐水性、耐水性及び耐汚損
性を備えた光沢を有する皮膜が残り、この被膜が
床面を保護する。床面に予め樹脂系ワツクスが塗
布されている場合には、その上からツヤ出し洗浄
剤を塗布し、該ツヤ出し洗浄剤の被膜が床面の表
層面に形成されるようにする。
この皮膜が汚れた場合には、同じツヤ出し洗浄
剤を含させたモツプ等で軽く拭く事により、ゴミ
や油汚れ等の被膜表面に固着した汚れは勿論、ブ
ラツクヒールマーク等の被膜に食い込んだ汚れも
容易に除去することができ、汚れが除去された後
にツヤ出し洗浄剤が乾燥して新たなコーテイング
被膜が形成され、これが新たに床面に光沢を与え
ると共に保護する。
前記汚れの除去機構は次のメカニズムによりな
されると考えられる。本発明のツヤ出し洗浄剤を
塗布し、これに含まれる前記重合体でコーテイン
グされた床面に固着した汚れは、このツヤ出し洗
浄剤をモツプ等にしみ込ませ軽く拭く事により、
ツヤ出し洗浄剤に含まれるアンモニア、アミン、
アミノアルコール類等がコーテイング皮膜のカル
ボキシル基と反応してカルボキシル基の塩とな
り、コーテイング被膜の再溶解が起り、コーテイ
ング皮膜に固着した汚れがコーテイング皮膜と共
に溶解してモツプ等に拭き取られ、汚れた重合体
と新しい重合体の交換がなされ、乾燥した後に汚
れの除去された光沢の良好なコーテイング被膜が
残ると考えられる。
こうして得られたコーテイング皮膜が耐水性を
有するには分子量が重量平均分子量で8000を越え
45000以下である事が必要である。(以下分子量は
重量平均分子量を言う)。分子量が8000以下にな
ると洗浄性及び光沢には優れているが、耐水性に
おいて大幅に劣り、他方分子量が、45000を超え
ると、耐水性及び光沢に優れているが洗浄力にお
いて著しく劣る。
本発明の目的を達するため、上記ツヤ出し洗浄
剤に他の助剤を加える事によりさらに効果を高め
る事ができる。洗浄性をさらに高めるには、アン
モニア或いはモルホリン等でPHを9または9以上
に高めると良いが、PH10を越えるとアンモニア臭
やアミン臭が強く使用上問題を生じる。さらに洗
浄力を与えるため水溶性溶剤類(例えばブチルセ
ルソルブ、ブチルカルビトール、N−メチルピロ
リドン等)を加えても良く、その他通常の非イオ
ン系活性剤(例えばノニルフエノールエチレンオ
キサイド付加物)、アニオン系活性剤(例えばド
デシルベンゼンスルホン酸ナトリウム等)、フツ
素系界面活性剤(例えば米国特許2937098号に記
載された界面活性剤等)、苛性類(例えば水酸化
ナトリウム等)等も添加しても良い。また耐水性
をさらに高めるために多価金属錯塩(例えば炭酸
亜鉛のアンミン錯体、亜鉛のアミノ酸錯体等)、
カルボキシル基又は水酸基と架橋可能な架橋剤
(例えばポリアジリジン化合物、水溶性エポキシ
化合物等)も加えても良い。またコーテイング皮
膜の光沢をさらに付与するため高沸点水溶性溶剤
類(例えばエチルカルビトール等)も加えても良
い。ゴミ類の付着防止の目的として、ワツクス類
(例えばポリエチレンワツクスの乳化物等)を加
えても良い。その他種々の目的のためアクリルエ
マルジヨンポリマー、ロジン変性マレイン酸樹
脂、スチレンマレイン酸樹脂、水溶性アクリル樹
脂(分子量8000未満又は50000を超えるもの)、消
泡剤等も加えても良いが、最少限にとどめておい
た方が良い。
−実施例−
次に本発明の実施例、特にツヤ出し洗浄剤の幾
つかの代表的な組成と該ツヤ出し洗浄剤を用いて
行つた試験の結果について記載する。以下の記載
におけるツヤ出し洗浄剤の組成は特に断らない限
り重量部を示す。
第1表の重合体No.1ないし4および参考例A,
Bの重合体に第2表の水および各種添加剤を順に
加えて撹拌機により混合し、試料1ないし4およ
び参考試料A,Bを得た。
-Field of Industrial Application- The present invention relates to a maintenance method for maintaining a clean and glossy surface of a building floor, particularly a plastic flooring material. -Prior Art- It has been conventional practice to apply a release agent to give gloss and cleanliness to the floor surfaces of buildings. When the flooring material is a plastic flooring material, a resin wax called a non-buffable type or a semi-buffable type is used as a release agent. The surface of the floor surface coated with such wax is protected by the resin wax and has gloss and stain resistance, but it is important to avoid loss of gloss due to use, stains due to black heel marks, and surface scratches. I can't do it. Therefore, it is necessary to periodically clean the surface to maintain cleanliness and gloss, that is, maintenance work. Conventional maintenance work for floors coated with resin-based wax is to remove dust from the floor, remove dirt with a cleaning agent, remove waste water from cleaning, dry, and re-apply resin-based wax to finish. This is done in the following steps. -Problems to be Solved by the Invention- However, the above cleaning process uses a large amount of water, so it must be carried out by moving the utensils installed on the floor, and it also requires the use of equipment such as a sewage suction device. The work is complicated, and if there are gaps in the floor surface, there is a problem that sewage may leak under the floor. However, with the conventional cleaning agents used in the above-mentioned cleaning process, it is difficult to remove dirt that has stuck to the surface of the floor or that has penetrated into the interior of the floor by simply wiping or washing it off. There's a problem. For example, vinyl tiles and vinyl asbestos tiles are widely used as flooring materials in offices, hospitals, etc., and resin-based wax is usually coated on top of these flooring materials. The scratches on the bottom (black heel marks) dig into the wax film and remain black. It is difficult to wash off this stain with ordinary cleaning agents, and in this case, it is necessary to remove it together with the resin wax using a cleaning agent called a ``removal agent'' containing cellosolve, which is extremely complicated. It is. On the other hand, a polishing agent is known in which an alkali-soluble resin that acts as a detergent and a surfactant are added to a resin-based wax, thereby cleaning old coatings at the same time as waxing. However, although this type of polishing agent can remove minor stains such as oil stains on the coating surface, it is completely impossible to remove stains that have dug into the coating film, such as black heel marks. Furthermore, addition of a large amount of alkali-soluble resin has the disadvantage that the function of the re-formed coating film as a protective film, particularly the water resistance, is greatly reduced. The purpose of this invention is to solve the above-mentioned conventional problems, and it does not require the conventional cleaning process using a cleaning agent or stripping agent, and can perform the conventional processes described above in one step. Therefore, it is extremely easy to keep the floor clean, and the floor surface can be protected with a coating film that has excellent gloss, strong water resistance, durability, and stain resistance. The purpose is to provide a cleanliness maintenance method. -Means for solving the problem- In the method of the present invention, a polishing cleaning agent is used to maintain the cleanliness of the floor surface. This polishing cleaning agent is a composition containing 6 to 24 percent by weight of a polymer having the following structural formula and having a weight average molecular weight of more than 8,000 and less than 45,000, and is an aqueous solution having a pH of 6.5 to 10. In the above structural formula, M is another vinyl monomer to be added and copolymerized if necessary, and R 1 is hydrogen or has 1 carbon number.
an alkyl group having 1 to 3 carbon atoms, R 2 has 1 carbon number
to 8 alkyl groups and hydrogen necessary to make the acid value 70 to 650 mg KOH per gram of polymer, m and n are the weight average molecular weight of the polymer of 8000
Represents the positive number necessary to exceed 45,000 and be less than 45,000. In the method of the present invention, a polishing cleaning agent made of the above-mentioned composition is applied to a floor surface coated with or not coated with a resin wax in advance and dried, and the polishing cleaning agent is dried on the surface layer of the floor surface. Forming a coating film formed by the above method. When the floor surface becomes soiled, wipe the floor surface with a mop or the like moistened with the above-mentioned polishing cleaning agent.
The old coating is redissolved to remove dirt and a new coating of the polishing cleaning agent is formed on the surface layer. The monomers of the polymer contained in this polish cleaning agent are randomly bonded. Examples of the monomer include methacrylic acid methyl ester, acrylic acid butyl ester, methacrylic acid, and acrylic acid, and if necessary, vinyl monomers such as acrylonitrile, vinyl acetate, and styrene can be used as a copolymer. Moreover, the acid value is adjusted by the amount of acrylic acid or methacrylic acid. The above monomers are polymerized by conventional solution polymerization, bulk polymerization, suspension polymerization, or emulsion polymerization. It is also effective to use a chain transfer agent to adjust the molecular weight. Mercaptans and halogenated carbons can be used as chain transfer agents, specifically dodecyl mercaptan, lauryl mercaptan,
Carbon tetrachloride, bromotrichloromethane, etc.
The molecular weight of the polymer varies depending on the polymerization conditions, but is roughly determined by the molar ratio of the chain transfer agent and the weight component.
Specific examples include U.S. Patent No. 2870116 and U.S. Patent No.
Examples are given in No. 2870117, Japanese Patent Publication No. 14019/1974, etc. Another method for adjusting the molecular weight is by adjusting the polymerization temperature, the concentration of the polymerization initiator, and the type of solvent for solution polymerization, as exemplified in JP-A-54-64532. The polymer thus obtained may contain a large amount of chain transfer agent and have a strange odor, or may be contaminated with solvents,
When a problem with residual monomer odor occurs, it is necessary to remove it. In such cases, it is possible to almost completely remove it by azeotropic removal with water, steam distillation, vacuum distillation, etc. It is.
The molecular weight of the polymer thus obtained can be easily measured by gel permeation chromatography (GPC method). In the polymer obtained above, the carboxyl group is neutralized with ammonium, an amine, or an amino alcohol to become a salt, exhibiting water solubility and dissolving in water, and exhibiting a pale yellow or colorless transparent or translucent appearance. -Function- When an aqueous solution of the above polymer, that is, a polish cleaning agent referred to in the present invention, is applied to a floor surface, the volatile components are dried and removed, resulting in a gloss with sufficient water resistance, water resistance, and stain resistance. A film remains that protects the floor surface. If a resin-based wax has been applied to the floor surface in advance, a polishing cleaning agent is applied thereon so that a film of the polishing cleaning agent is formed on the surface layer of the floor surface. If this film becomes dirty, gently wipe it with a mop moistened with the same polishing detergent to remove dirt that has stuck to the film surface, such as dust and oil stains, as well as dirt that has burrowed into the film, such as black heel marks. Dirt can also be easily removed, and once the stain has been removed, the polishing agent dries to form a new coating that adds shine and protection to the floor. The dirt removal mechanism is considered to be performed by the following mechanism. The stains that have adhered to the floor coated with the polymer contained in the polishing cleaning agent of the present invention can be removed by soaking the polishing cleaning agent into a mop or the like and gently wiping it.
Ammonia, amines, and
Amino alcohols, etc. react with the carboxyl group of the coating film to form a salt of the carboxyl group, and the coating film is redissolved, and the dirt stuck to the coating film is dissolved together with the coating film and wiped off with a mop etc., making it dirty. It is believed that the polymer is replaced with fresh polymer, leaving a clean, glossy coating after drying. For the coating film obtained in this way to have water resistance, the molecular weight must exceed 8000 in terms of weight average molecular weight.
It must be less than 45,000. (The molecular weight below refers to the weight average molecular weight.) When the molecular weight is less than 8,000, it has excellent detergency and gloss, but it is significantly inferior in water resistance, while when the molecular weight exceeds 45,000, it is excellent in water resistance and gloss, but it is extremely inferior in detergency. In order to achieve the object of the present invention, the effect can be further enhanced by adding other auxiliary agents to the above polishing cleaning agent. In order to further improve the cleaning performance, it is preferable to raise the pH to 9 or above with ammonia or morpholine, but if the pH exceeds 10, the ammonia odor or amine odor will be strong, causing problems in use. Furthermore, water-soluble solvents (e.g., butyl cellosolve, butyl carbitol, N-methylpyrrolidone, etc.) may be added to provide additional cleaning power, and other ordinary nonionic surfactants (e.g., nonylphenol ethylene oxide adduct), Anionic surfactants (e.g., sodium dodecylbenzene sulfonate, etc.), fluorine-based surfactants (e.g., the surfactants described in U.S. Pat. No. 2,937,098, etc.), caustics (e.g., sodium hydroxide, etc.) are also added. Also good. In addition, to further increase water resistance, polyvalent metal complex salts (e.g. ammine complex of zinc carbonate, amino acid complex of zinc, etc.),
A crosslinking agent capable of crosslinking with a carboxyl group or a hydroxyl group (for example, a polyaziridine compound, a water-soluble epoxy compound, etc.) may also be added. Furthermore, high boiling point water-soluble solvents (for example, ethyl carbitol, etc.) may be added to further impart gloss to the coating film. For the purpose of preventing dust from adhering, waxes (for example, emulsions of polyethylene wax, etc.) may be added. Acrylic emulsion polymers, rosin-modified maleic acid resins, styrene maleic acid resins, water-soluble acrylic resins (molecular weight less than 8,000 or more than 50,000), antifoaming agents, etc. may also be added for various other purposes, but the minimum It is better to keep it at that. -Examples- Next, Examples of the present invention will be described, in particular, some representative compositions of polishing cleaning agents and the results of tests conducted using the polishing cleaning agents. The composition of the polishing cleaning agent in the following description is in parts by weight unless otherwise specified. Polymer Nos. 1 to 4 in Table 1 and Reference Example A,
Water and various additives listed in Table 2 were added to the polymer B in order and mixed using a stirrer to obtain Samples 1 to 4 and Reference Samples A and B.
【表】
(表中、MMAはメタクリル酸メチル、BAはア
クリル酸ブチル、STはスチレン、ANはアクリ
ロニトリル、MAAはメタクリル酸、AIBNはア
ゾビスイソブチロニトリルである。分子量は高速
体クロマトグラフイーHLC−802UR(GPC、東洋
ソーダ社製)で測定した。)[Table] (In the table, MMA is methyl methacrylate, BA is butyl acrylate, ST is styrene, AN is acrylonitrile, MAA is methacrylic acid, and AIBN is azobisisobutyronitrile. The molecular weight is determined by high performance chromatography. Measured with HLC-802UR (GPC, manufactured by Toyo Soda Co., Ltd.)
【表】【table】
【表】
得られた各試料を白色のビニールタイルに15
g/m2の割合で塗布し、12時間常温で乾燥し、次
いで耐ブラツクヒールマークテスト機(スネルカ
プセルテスト機、米国CSMA Bulletin No.9−
73)でブラツクヒールマークを付けた。次に当該
試料をモツプにしみ込ませてブラツクヒールマー
クを付けたビニールタイル面を軽く拭き、ブラツ
クヒールマークの汚れ落ち具合を観察し、洗浄性
を調べた。
次に黒色のビニールタイル面に上記各試料を15
g/m2の割合で塗布し、12時間常温で乾燥した。
次いで再度当該試料をモツプにしみ込ませて15
g/m2の割合で塗布し、12時間常温で乾燥した
後、該タイル表面の光沢、レベリング性、耐水性
を評価した。光沢は米国CSMAD1455−64の60゜
鏡面反射率で測定した。レベリング性はモツプ塗
布跡の少さ(平滑性)を肉眼で評価した。耐水性
は、塗布タイルに1mlの水を滴下して1時間放置
し、水を拭き取つて乾燥した後、白く跡が残る程
度を肉眼で評価した。
評価結果を第3表に示す。[Table] Each sample obtained was placed on a white vinyl tile.
g/ m2 , dried at room temperature for 12 hours, and then tested using a black heel mark tester (Snell Capsule Tester, US CSMA Bulletin No.9-
73) with a black heel mark. Next, the sample was soaked into a mop and the surface of the vinyl tile bearing the black heel mark was gently wiped, and the degree of stain removal of the black heel mark was observed to examine the cleanability. Next, place 15 of each of the above samples on the black vinyl tile surface.
It was applied at a rate of g/m 2 and dried at room temperature for 12 hours.
Next, let the sample soak into the mop again 15
After coating at a ratio of g/m 2 and drying at room temperature for 12 hours, the gloss, leveling property, and water resistance of the tile surface were evaluated. Gloss was measured using 60° specular reflectance of US CSMAD1455-64. The leveling property was evaluated visually based on the lack of motu application marks (smoothness). Water resistance was evaluated by dropping 1 ml of water onto the coated tile, leaving it for 1 hour, wiping off the water, drying, and visually evaluating the extent to which white marks remained. The evaluation results are shown in Table 3.
【表】
−発明の効果−
以上説明した本発明の方法によれば、従来の床
面のメンテナンス作業で必要とした洗浄水による
洗浄作業及び汚水の除去作業(後拭き等)が不要
となり、きわめて簡単な作業で床面を清浄に維持
することができ、ブラツクヒールマーク等も容易
に落すことができる。そしてこの発明の方法で処
理された床面は、ツヤ出し洗浄剤中の水分が蒸発
してその中に含まれた重合体によるコーテイング
皮膜が形成され、優れた光沢が付与され、頻繁な
水拭きにも耐える耐水性、強靭な耐久性、耐汚損
性を備えた面に仕上り、土足で歩行する床面であ
つても、充分に清浄に維持することができる。
そして上記実施例によつても明らかな如く、本
発明方法で用いられるツヤ出し洗浄剤は、洗浄性
と耐水性のバランス良く、良好な光沢と優れたレ
ベリング性を備えている。[Table] - Effects of the Invention - According to the method of the present invention explained above, the cleaning work with washing water and the work of removing waste water (after-wiping, etc.), which were required in conventional floor maintenance work, are no longer necessary, and it is extremely effective. You can keep the floor clean with a simple operation, and black heel marks can be easily removed. The floor surface treated by the method of this invention has a coating film formed by the polymer contained therein as the moisture in the gloss cleaning agent evaporates, giving it an excellent gloss and requiring frequent wiping with water. The surface is finished with water resistance, strong durability, and stain resistance, and can be kept sufficiently clean even on floors where you walk on with shoes on. As is clear from the above examples, the polishing cleaning agent used in the method of the present invention has a good balance of cleaning performance and water resistance, and has good gloss and excellent leveling properties.
Claims (1)
床面に重量平均分子量が8000を越え45000以下の
下記構造式を有する重合体を重量パーセントで6
ないし24パーセント含みPHを6.5ないし10の範囲
に調整した水溶液を塗布して該床面の表層面にコ
ーテイング被膜を形成し、該床面が汚損されたと
きに前記水溶液で拭いて表層面の古い被膜の溶解
除去による床面の洗浄と新たなコーテイング被膜
の形成とを同時に行うことを特徴とする、床面の
表面清浄維持方法。 但し、式中Mは必要により付加共重合する他の
ビニールモノマー、R1は水素または炭素数1な
いし3個を有するアルキル基、R2は炭素数1な
いし8個のアルキル基および酸価を重合体1グラ
ム当たり70ないし650mgKOHにするに必要な水
素、m,nは前記重合体の重量平均分子量を8000
を越え45000以下とするに必要な正数を表わす。[Scope of Claims] 1. A polymer having the following structural formula with a weight average molecular weight of more than 8,000 and less than 45,000 is applied to a floor surface with or without resin wax applied in advance in weight percent of 6.
A coating film is formed on the surface layer of the floor by applying an aqueous solution containing 24% to 24% and adjusting the pH to a range of 6.5 to 10. When the floor surface becomes soiled, it is wiped with the aqueous solution to remove the old surface layer. A method for maintaining the surface cleanliness of a floor surface, characterized by cleaning the floor surface by dissolving and removing the film and forming a new coating film at the same time. However, in the formula, M is another vinyl monomer to be addition-copolymerized if necessary, R 1 is hydrogen or an alkyl group having 1 to 3 carbon atoms, and R 2 is an alkyl group having 1 to 8 carbon atoms and an acid value. Hydrogen required to make 70 to 650 mg KOH per gram of coalesce, m and n are the weight average molecular weight of the polymer 8000
Represents the positive number necessary to exceed 45,000 and be less than 45,000.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14753587A JPS62294471A (en) | 1987-06-13 | 1987-06-13 | Method for keeping cleanliness of floor surface |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14753587A JPS62294471A (en) | 1987-06-13 | 1987-06-13 | Method for keeping cleanliness of floor surface |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15017281A Division JPS5852399A (en) | 1981-09-22 | 1981-09-22 | Polishing detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62294471A JPS62294471A (en) | 1987-12-21 |
JPH0448510B2 true JPH0448510B2 (en) | 1992-08-06 |
Family
ID=15432510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14753587A Granted JPS62294471A (en) | 1987-06-13 | 1987-06-13 | Method for keeping cleanliness of floor surface |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62294471A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02106555A (en) | 1988-10-14 | 1990-04-18 | Brother Ind Ltd | Tape containing cassette |
JPH0776326B2 (en) * | 1991-06-19 | 1995-08-16 | フクビ化学工業株式会社 | Floor wax |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5394344A (en) * | 1977-01-31 | 1978-08-18 | Morizou Nakamura | Aqueous coating composition |
-
1987
- 1987-06-13 JP JP14753587A patent/JPS62294471A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5394344A (en) * | 1977-01-31 | 1978-08-18 | Morizou Nakamura | Aqueous coating composition |
Also Published As
Publication number | Publication date |
---|---|
JPS62294471A (en) | 1987-12-21 |
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