JPS63221179A - Release agent composition for resin wax film - Google Patents
Release agent composition for resin wax filmInfo
- Publication number
- JPS63221179A JPS63221179A JP5491687A JP5491687A JPS63221179A JP S63221179 A JPS63221179 A JP S63221179A JP 5491687 A JP5491687 A JP 5491687A JP 5491687 A JP5491687 A JP 5491687A JP S63221179 A JPS63221179 A JP S63221179A
- Authority
- JP
- Japan
- Prior art keywords
- water
- weight
- release agent
- composition
- peeling
- 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
- 239000011347 resin Substances 0.000 title abstract description 25
- 229920005989 resin Polymers 0.000 title abstract description 25
- 239000000203 mixture Substances 0.000 title abstract description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229920002125 Sokalan® Polymers 0.000 claims abstract description 15
- 239000004584 polyacrylic acid Substances 0.000 claims abstract description 14
- 239000003513 alkali Substances 0.000 claims abstract description 11
- 239000003960 organic solvent Substances 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000002736 nonionic surfactant Substances 0.000 claims description 5
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 230000001747 exhibiting effect Effects 0.000 claims 1
- -1 polyoxyethylene Polymers 0.000 abstract description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 8
- 239000005977 Ethylene Substances 0.000 abstract description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 3
- 239000004094 surface-active agent Substances 0.000 abstract description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 abstract description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract description 2
- 239000012670 alkaline solution Substances 0.000 abstract description 2
- 229920000570 polyether Polymers 0.000 abstract description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 49
- 230000000052 comparative effect Effects 0.000 description 9
- 238000005498 polishing Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000007865 diluting Methods 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000003973 alkyl amines Chemical class 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 230000002925 chemical effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000019795 sodium metasilicate Nutrition 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 239000003021 water soluble solvent Substances 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- NHWZQIYTQZEOSJ-UHFFFAOYSA-N carbonic acid;phosphoric acid Chemical class OC(O)=O.OP(O)(O)=O NHWZQIYTQZEOSJ-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 235000007686 potassium Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- RLQWHDODQVOVKU-UHFFFAOYSA-N tetrapotassium;silicate Chemical compound [K+].[K+].[K+].[K+].[O-][Si]([O-])([O-])[O-] RLQWHDODQVOVKU-UHFFFAOYSA-N 0.000 description 1
- POWFTOSLLWLEBN-UHFFFAOYSA-N tetrasodium;silicate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-] POWFTOSLLWLEBN-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は樹脂ワックス等床用艶出し剤の膜を剥離する剥
離剤組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a stripping agent composition for stripping a film of a floor polish such as a resin wax.
[従来の技術]
一般に、床等に用いられる樹脂ワックス艶出し剤は、金
属架橋型アクリル樹脂エマルジョンを主成分としてポリ
エチレンエマルジ曹ン、レジン。[Prior Art] Generally, resin wax polishing agents used for floors etc. are mainly composed of metal crosslinked acrylic resin emulsion, polyethylene emulsion carbonate, and resin.
可塑剤などの配合物である。この様な樹脂ワックス艶出
し剤は、塗布後の乾燥過程に於いて金属架橋型アクリル
樹脂中のカルボキシル基どうしが。It is a compound such as a plasticizer. In such a resin wax polishing agent, the carboxyl groups in the metal crosslinked acrylic resin bond together during the drying process after application.
Znなどの金属原子で架橋され歩行などに十分耐えうる
強靭な被膜となる。金属架橋されたカルボキシル基変性
アクリルポリマーの被膜は、アンモニウムイオンと架橋
金属とが錯塩をつくるため、架橋結合を切断することが
できる。その結果、カルボキシル基は自由になりアルカ
リによりナトリウムJ!!なととなり水に可溶となる。Cross-linked with metal atoms such as Zn, it becomes a tough coating that can withstand walking. In the metal-crosslinked carboxyl group-modified acrylic polymer film, ammonium ions and the crosslinked metal form a complex salt, so the crosslinks can be broken. As a result, the carboxyl group becomes free and the alkali causes sodium J! ! It becomes soluble in water.
この性質を利用し通常′Amがおこなわれ、そのための
剥離剤が種々市販されており、一般に床等のメンテナン
スでは、長期間の歩行などにより傷付3.g美観を失っ
た樹脂ワックス被膜を強いアルカリ性の剥離剤を用い完
全に」離除去した後、新たな樹脂ワックスなどの艶出し
剤を塗布し美観を回復させている。Utilizing this property, 'Am' is usually carried out, and various stripping agents for this purpose are commercially available.In general, when maintaining floors, etc., it is difficult to remove scratches caused by long-term walking, etc. After the resin wax coating that has lost its aesthetic appearance is completely removed using a strong alkaline remover, a new polishing agent such as resin wax is applied to restore the aesthetic appearance.
従来使用されている剥離剤は、水溶性溶剤、アルカリビ
ルグー、界面活性剤、アミンなどを主成分としており、
これを5〜10倍の水で希釈して使用されている。かか
る希釈液を用いた剥離作業は、まず剥離剤希釈液をモツ
プ等で均一に被膜上に塗布する0時間をおき被膜をある
程度溶解あるいは膨潤させた後、ポリフシャーを用い剥
離専用バットで充分に被膜を研磨除去する。ついで汚水
を回収し充分な水拭きを行うものである。この一連の作
業中ポリラシャ−を使用し充分に被膜を研磨することが
確実な剥離作業に不可欠であった。Conventionally used stripping agents are mainly composed of water-soluble solvents, alkaline bilges, surfactants, amines, etc.
This is used by diluting it 5 to 10 times with water. Peeling work using such a diluted solution involves first applying the diluted stripping agent solution uniformly onto the film with a mop, etc. After waiting for 0 hours to dissolve or swell the film to some extent, use a polisher to thoroughly coat the film with a special stripping vat. Remove by polishing. The waste water is then collected and thoroughly wiped down. During this series of operations, it was essential to thoroughly polish the coating using a poly lasher to ensure reliable peeling.
しかしながらポリラシャ−の使用は、過酷な作業であり
、かつ熟練を要し、更に狭く入り組んだ場所や階段など
では使用出来ないなどの問題点がありながら一般に用い
られている。なぜなら、オフィスビル、スーパーマーケ
ットあるいはテハート等に於ける剥離作業は人々の帰っ
た後の夜間に行なわれることが一般的であり作業時間に
制約がある。この限られた時間内に作業を終了するため
には剥離作業の各工程が確実でなければならない、した
がって、現在一般に使用されているUs剤では確実な剥
離作業を行うためにポリラシャ−の使用が不可欠である
。However, the use of poly lashers is difficult and requires skill, and is generally used despite the problems that it cannot be used in narrow and intricate places or stairs. This is because stripping work in office buildings, supermarkets, Tehart stores, etc. is generally carried out at night after people have gone home, and there are restrictions on work time. In order to complete the work within this limited time, each step of the peeling work must be performed reliably.Therefore, with the currently commonly used Us agent, it is necessary to use Polylasha to perform the peeling work reliably. It is essential.
[発明が解決しようとする問題点]
従来の剥離剤あるいはその爲釈液は、低粘度ニュートン
液体であるため非常に流れ易い、このため、使用時、床
に設置されている例えばロッカー、書棚などの下に剥離
剤が流れこんでいた。[Problems to be Solved by the Invention] Conventional stripping agents or their dissolution liquids are low-viscosity Newtonian liquids, so they flow very easily. Therefore, when used, they can be used on lockers, bookshelves, etc. installed on the floor. Remover had flowed underneath.
これを作業中に全て回収することは難しく、剥離作業終
了後にしみ出ていた。これは新たに塗布した樹脂ワック
ス被膜を侵してしまい、さらには原剤の変色等をきたし
著しく美観を損ねる原因となっていた。そこでこの様な
恐れのある場合は、マスキングテープ等を用いg*剤が
流れ込むことを防止していた。しかし広いスペースでは
非常に手間のかかる作業であるため、剥離剤の塗布から
回収までの間、流れ広がることのない剥離剤が望まれて
いた。It was difficult to collect all of this during the work, and it seeped out after the peeling work was completed. This corrodes the newly applied resin wax coating and further causes discoloration of the raw material, resulting in a significant loss of aesthetic appearance. Therefore, in cases where such a possibility exists, masking tape or the like is used to prevent the g* agent from flowing into the container. However, since it is a very labor-intensive task in a large space, there was a desire for a remover that would not run and spread during the period from application to collection.
また、従来の剥離剤が低粘度ニュートン液体であること
は、剥離しようとする樹脂ワックス膜上に、均一に充分
厚く塗布することを不可能としていた。これは塗布した
剥離剤を薄くし蒸発乾燥をまねく原因となっていた。こ
の乾燥した部分は再び被膜を形成してしまうので、水拭
き工程で除去することは出来ず剥離残しとなる。この様
な場合は、再度の剥離作業が必要となり手間がかかる以
上に、予定時間内に作業を終了出来ないという問題が起
きてしまう、また、薄い剥離剤では被膜に対する剥離剤
の絶対量が少なく、充分に被膜を溶解させることは難し
い、このことがポリシャー使用を不可欠にしており、さ
らに被膜を一部溶解あるいは膨潤させ、蒸発により少量
となった剥離剤は高粘度となり回収作業に手間取ってい
た。この場合は再度の剥離剤や水の塗布が必要となり先
に上げた剥離剤の流れ広がりの問題となる。したがって
、乾燥しにくく一度の塗布作業で完全な剥離を可謝とす
る強力な剥離剤が望まれていた。Furthermore, the fact that conventional stripping agents are low-viscosity Newtonian liquids has made it impossible to uniformly and sufficiently thickly coat the resin wax film to be stripped. This caused the applied release agent to become thinner and cause it to evaporate and dry. Since this dried part forms a film again, it cannot be removed in the wet wiping process and remains unpeeled. In such cases, the removal work is required again, which is not only time-consuming but also causes the problem that the work cannot be completed within the scheduled time.Also, if the release agent is thin, the absolute amount of the release agent against the film is small. However, it is difficult to sufficiently dissolve the film, which makes it necessary to use a polisher.Furthermore, the film partially dissolves or swells, and the small amount of remover that evaporates becomes highly viscous, making recovery work time-consuming. . In this case, it is necessary to apply the release agent or water again, resulting in the problem of the release agent flowing and spreading as mentioned earlier. Therefore, there has been a demand for a strong release agent that does not dry easily and allows complete removal with a single application.
また、剥離作業の現場には、出来る限り従来の剥離剤や
水の使用を制限したい場所例えばフリーアクセスフロア
−がある、フリーアクセスフロア−は配線や配管が集中
化していて、さらにその点検および交換が必要な床に用
いられる0例えばコンピューター室、スタジオなどがそ
の対象となっている。フリーアクセスフロア−ではコン
クリートスラブとタイルの置かれる床の間に数10CI
の空間があり、この空間に配線や配管される。In addition, stripping work sites include areas where it is desirable to limit the use of conventional stripping agents and water as much as possible, such as raised floors, where wiring and piping are concentrated, and inspection and replacement of these. For example, computer rooms, studios, etc., which are used for floors that require Raised floors - several tens of CIs between the concrete slab and the floor where the tiles are placed.
There is a space in which wiring and piping will be installed.
これらの床は50cm四方に区切られ取りはずし可能と
なっていることが多〈従来の剥離剤や水では、そのすき
まから床下の空間に流れ落ちてしまいショート、漏電、
腐蝕等の原因となる。このため充分に対応出来ないケー
スも見られ、さらに今後この様な現場は増えると思われ
る。したがって必要最低限の水使用でかつ流れ落ちるこ
とのない剥離剤の開発が急務となっている。These floors are often divided into 50 cm square sections and are removable. (Conventional stripping agents and water can run down through the gaps into the space under the floor, causing short circuits, electrical leaks, and
It may cause corrosion etc. As a result, there are some cases where we are unable to respond adequately, and it is expected that the number of such cases will increase in the future. Therefore, there is an urgent need to develop a stripping agent that uses the minimum necessary amount of water and does not run off.
また、樹脂ワックスが塗布される床のなかには、通常の
平面なタイルの外に最近エンボスタイプと呼ばれるタイ
ル表面を凹凸前■したものが表われている。この様なタ
イルを用いた現場では、従来ポリラシャ−の使用を前提
とした作業は難しい、即ち、四部のポリラシャ一作業が
不充分となり剥離残しと成り易い、この場合単にポリラ
シャ−不要の強力な剥離剤であっても、従来通りの流動
性に富みすぎたものでは、やはり凸部において剥離残し
となる。したがって、ポリラシャ−不要でなおかつタイ
ルの凹凸部を均一に塗布可能とするチキントロピック性
を兼ね備えた!4離剤が望まれている。Furthermore, in addition to regular flat tiles, embossed tiles with an uneven surface have recently appeared among the floors to which resin wax is applied. At sites where such tiles are used, it is difficult to perform work that requires the use of conventional poly lashers.In other words, the four-part poly lasher work is insufficient and tends to leave peeling residue. Even if the agent is too fluid as in the past, it will still leave peeling residue on the convex portions. Therefore, it does not require a poly lasher and has chicken tropic properties that allow it to be applied evenly to uneven parts of tiles! 4 release agent is desired.
また、床面には、コーナー、巾木、机の下などのポリラ
シャ−を使用できない部分も多くある。Furthermore, there are many areas on the floor where polyrushers cannot be used, such as corners, baseboards, and under desks.
このような部分では、剥離剤塗布後、全て手作業により
バットで床面を研磨する必要があり非能率的であった。In such areas, it was necessary to polish the floor surface manually with a bat after applying the release agent, which was inefficient.
したがって、剥離作業の容易な研磨作業の必要な剥離剤
が1まれでいた。Therefore, there was only one release agent that required a polishing operation to facilitate the removal operation.
更にまた。樹脂ワックス艶出し剤が塗布される部分は、
平面なる床以外に階段などの垂直面もある。ここでの作
業は通常の方法で完全に剥離できず、特に剥離剤を垂直
面に保持させることは難しく非能率的な手作業に頼らざ
るをえなかった。したがって垂直面においても、たれ落
ちることのない′A離剤が望まれていた。Yet again. The area where the resin wax polish is applied is
In addition to flat floors, there are also vertical surfaces such as stairs. In this work, it was not possible to completely remove the film using normal methods, and in particular, it was difficult to hold the release agent on a vertical surface, and it was necessary to rely on inefficient manual methods. Therefore, there has been a desire for a 'A release agent that does not drip even on vertical surfaces.
以上の様な問題点を克服した樹脂ワックス艶出し剤のた
めの剥離剤はいまだに開発されていない。A release agent for resin wax polishing agents that overcomes the above-mentioned problems has not yet been developed.
従来の剥離剤は、先に述べた様に水溶性溶剤。Conventional stripping agents are water-soluble solvents, as mentioned earlier.
アルカリビルグー、界面活性剤、アミンなどから構成さ
れるものが一般的であり、低粘度ニュートン溶液であっ
た。かかる剥離剤の問題点の解決として増粘剤を添加し
、高粘度かつチキントロピック性を付与させる事は一つ
の方法と考えられる。It is generally a low-viscosity Newtonian solution composed of alkaline bilge, surfactants, amines, etc. One way to solve these problems with release agents is to add a thickener to impart high viscosity and chicken-tropic properties.
しかし単に従来の剥離剤に増結剤を加えることは、いく
つかの点で問題があり使用出来無かった。まず剥離剤の
水素イオン濃度は、工4に近く強アルカリ性であり、さ
らに多種多酸のイオン性物質、例えばメタケイ酸ソーダ
などの無機アルカリ、陰イオン界面活性剤、可溶化剤な
どが含まれるため水溶性ポリマーを用いた場合は、ポリ
で−が塩析や加水分解を起し安定性を具備した剥離剤組
成物を開発することは難しい、また無機系の増粘剤は、
水溶性で無いため剥離作業終了後残留してしまい、新た
な樹脂ツー2クス塗布時に樹脂ワックスが白化現象を起
こしてしまい使用することはできない。However, simply adding a binder to a conventional stripping agent has several problems and cannot be used. First, the hydrogen ion concentration of the stripping agent is close to that of Step 4, and it is strongly alkaline, and it also contains ionic substances such as a wide variety of acids, such as inorganic alkalis such as sodium metasilicate, anionic surfactants, and solubilizing agents. When a water-soluble polymer is used, it is difficult to develop a stable release agent composition due to salting out and hydrolysis.
Since it is not water-soluble, it remains behind after the peeling process is completed, and when a new resin wax is applied, the resin wax causes a whitening phenomenon and cannot be used.
さらに開離剤は、通常5〜10倍に水で希釈使用される
ため、使用時に流れ広がりや、たれ落ちない程の粘度と
チキソトロピック性を持たせるためには、希釈前剥離剤
の粘度は非常に高いものとなる。これは、製造時の攪拌
や容器への充填あるいは、使用時の容器からの取り出し
に支障をきたしてしまう。Furthermore, since the release agent is usually diluted 5 to 10 times with water, the viscosity of the release agent before dilution must be adjusted to ensure viscosity and thixotropic properties that will not spread or drip during use. It will be very expensive. This poses a problem in stirring during production, filling the container, or removing the product from the container during use.
したがって、製造から使用時希釈するまでの間は、流動
性に富み、iqs作業直前に水で希釈することにより初
めて目的の粘度を発現するものが好ましい。Therefore, it is preferable that the agent has good fluidity from manufacture to dilution before use, and that the desired viscosity is achieved only when diluted with water immediately before the iqs operation.
さらに、従来の剥離剤は作業時にポリラシャ−(物理的
効果)を用いることを前提とし配合されている。このた
め通常の希釈倍率では金属架橋型アクリル樹脂のアルカ
リ水溶液可溶性に基づく化学的効果だけでは充分な剥離
は行なえなかった。まれに2〜3倍の低希釈率で使用さ
れるが、粘度は低く、かかる問題を全て解決するには至
らない。Furthermore, conventional release agents are formulated on the premise that polylashes (physical effects) will be used during work. For this reason, sufficient peeling could not be achieved by chemical effects based on the solubility of the metal crosslinked acrylic resin in aqueous alkaline solutions at normal dilution ratios. Although it is rarely used at a dilution rate as low as 2 to 3 times, the viscosity is low and this does not solve all of these problems.
ここに、本発明者らは、剥離剤使用時の水希釈によって
粘度を増加させることで、従来剥離剤を保持させること
の難しかった現場においても使用を可能とし、さらに樹
脂ワックス膜に均一に充分厚く塗布可能とすることで最
大限に化学的効果を発揮せしめ、かつ乾燥をおさえるこ
とにより、除去しようとする樹脂ワックス膜との接触有
効時間を長くすることによりポリシャー不要なる新規な
剥離剤組成物を発明した。By increasing the viscosity of the release agent by diluting it with water when using the release agent, the present inventors have made it possible to use it even in the field where it was difficult to retain the release agent in the past, and they have also made it possible to apply it evenly and sufficiently to the resin wax film. A new stripping agent composition that can be applied thickly to maximize the chemical effect, and by suppressing drying, it prolongs the effective time of contact with the resin wax film to be removed, eliminating the need for a polisher. invented.
[問題点を解決するための手段]
この発明は、丁記(A)ないしくF) I&分からなり
PH>10のアルカリ性を示す樹脂ワックスM!A離剤
組成物である。[Means for Solving the Problems] The present invention provides a resin wax M which is composed of (A) or F) I&and exhibits alkalinity with a pH>10! A release agent composition.
(A)次の一般式(I)で示される水溶性有機溶剤20
〜80重量2
R−0−(R’0)nH11@ 1111 ([)(式
中Rは炭素fi1〜4のアルキル基、フェニル基あるい
はベンジル基を示し、R′はエチレン基又はプロピレン
基あるいはその両方、nは1〜3)(B)水溶性ポリア
クリル酸 0.1〜5重量2(C)非イオン性界面
活性剤 0.1〜5重量2(D) 多価7にコ−/
l/ 0.1〜20重量2(E)無機もし
くは有機アルカリ 1〜15重量2(F)水
35〜75重量5(A)の成分の
水溶性有機溶剤は、次の一般式(I)で示される水溶性
有機溶剤で、炭素数1〜4の一価アルコール又は、フェ
ノール、ベンジンアルコールに酸化エチレン又は酸化プ
ロピレンあるいは両方を1〜3モル付加させたものであ
る。(A) Water-soluble organic solvent 20 represented by the following general formula (I)
~80 weight 2 R-0-(R'0)nH11@1111 ([) (In the formula, R represents an alkyl group with 1 to 4 carbon fi, a phenyl group, or a benzyl group, and R' is an ethylene group, a propylene group, or Both, n is 1 to 3) (B) Water-soluble polyacrylic acid 0.1 to 5 weight 2 (C) Nonionic surfactant 0.1 to 5 weight 2 (D) Co-/
l/0.1-20 weight 2 (E) inorganic or organic alkali 1-15 weight 2 (F) water
35-75 The water-soluble organic solvent of component 5 (A) by weight is a water-soluble organic solvent represented by the following general formula (I), which is oxidized to a monohydric alcohol having 1 to 4 carbon atoms, phenol, or benzine alcohol. It contains 1 to 3 moles of ethylene or propylene oxide, or both.
R−0−(R’0)nHe m * e (I)(式中
Rは炭素数1〜4のアルキル基、フェニル基、ベンジル
基を示し、R′はエチレン基又はプロピレン基あるいは
その両方、nは1〜3)例えば、エチレングリコールモ
ノn−ブチルエーテル、ジエチレングリコールモノエチ
ルエーテル、ブはピレングリコールモツプaビルエーテ
ルなどがあげられ、これらの一種単独または二種以上の
組合せが可能である。R-0-(R'0)nHe m * e (I) (in the formula, R represents an alkyl group having 1 to 4 carbon atoms, a phenyl group, a benzyl group, and R' is an ethylene group or a propylene group, or both, n is 1 to 3) For example, ethylene glycol mono-n-butyl ether, diethylene glycol monoethyl ether, pyrene glycol motu-a-yl ether, etc. can be mentioned, and these types can be used alone or in combination of two or more types.
(B)成分の水溶性ポリアクリル酸としては、架橋型ア
クリル酸重合体といわれるものの使用が好ましい、それ
はオレフィン系不飽和カルボン酸、例えばアクリル酸、
メタクリル酸などと、種々の多価アルコール、例えばポ
リアルケニルポリエーテルなどとの共重合物である。こ
の構造を有する水溶性ポリアクリル酸は、数種のものが
市販されており、例えば、ハイビスワコ−103(カル
ボキシル基含量57.7〜83.4%、0.2’1.中
和液粘度13,000〜40.0OOcp;和光純薬工
業株式会社製)を挙げることができる。これらを、一種
単独または二種以上の組み合わせで使用出来る。As the water-soluble polyacrylic acid of component (B), it is preferable to use what is called a crosslinked acrylic acid polymer, which is an olefinically unsaturated carboxylic acid such as acrylic acid,
It is a copolymer of methacrylic acid or the like and various polyhydric alcohols such as polyalkenyl polyethers. Several types of water-soluble polyacrylic acid having this structure are commercially available, such as Hibis Wako-103 (carboxyl group content 57.7-83.4%, 0.2'1. Neutralized liquid viscosity 13 ,000 to 40.0OOcp; manufactured by Wako Pure Chemical Industries, Ltd.). These can be used singly or in combination of two or more.
(C)成分の非イオン界面活性剤は、例えば、エチレン
の平均付加モル数6〜30で炭素数8〜22の第一級ま
たは第二級アルキル基のポリオ午ジエチレンアルキルエ
ーテル、エチレンの平均付加モル数6〜30でアルキル
基の炭素数が8〜16のポリオキシエチレンアルキルフ
ェニルエールなどが挙げられる。一般に洗浄剤、浸透剤
、a滑剤として利用される分子量範囲のものの全てを使
用出来る。The nonionic surfactant of component (C) is, for example, polyethylene diethylene alkyl ether having a primary or secondary alkyl group having 8 to 22 carbon atoms and an average number of moles of ethylene added of 6 to 30; Examples include polyoxyethylene alkylphenyl ale having a mole number of 6 to 30 and an alkyl group having 8 to 16 carbon atoms. Any molecular weight range commonly used as detergents, penetrants, and lubricants can be used.
(D)成分の多価アルコールとして、例えばエチレング
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
、トリメチレングリコール。Examples of the polyhydric alcohol of component (D) include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, and trimethylene glycol.
ブタンジオール、l#5−ベンタンジオール、ヘキシレ
ングリコール、グリセリンなどが挙げられ、これらの一
種単独または二種以上の組み合わせで使用できる。Examples include butanediol, l#5-bentanediol, hexylene glycol, glycerin, etc., and these can be used alone or in combination of two or more.
(E)成分として、ナトリウム、カリウムなどのアルカ
リ金属の水酸化物、炭酸基リン酸塩、およびケイ酸塩な
どの例えば水酸化ナトリウム、水酸化カリウム、炭酸ナ
トリウム、炭酸カリウム、リン酸ナトリウム、リン酸カ
リウム、メタケイ酸ナトリウム、メタケイ酸カリウム、
オルソケイ酸ナトリウム、オルソケイ酸カリウムなどの
無機アルカリが挙げられる。またアンモニア水や有機ア
ルカリとしては、アルキルアミン、アルカノ−ルアいノ
尼謂ナフ;ソ 苓糞故フいノmlハ01ギこれる0例
えばアルキルアミンとしては、モノエチルアミン、ジエ
チルアミン、トリエチルアミンなどであり、アルカノー
ルアミンとしてはモノエタノールアミン、ジェタノール
アミン、トリエタノールアミンなどであり、脂環式アミ
ンとしてはモルホリンなどがある。更にはエチレンジア
ミン、ジエチレントリアミン、トリエチレンテトラミン
、テトラエチレンペンタミン、ペンタエチレンへギサミ
ン、ピペランジンなどのエチレンアミンやプロピレンア
ミンを用いる事が出来る。(E) Components include alkali metal hydroxides such as sodium and potassium, carbonate phosphates, and silicates such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium phosphate, and phosphorus. acid potassium, sodium metasilicate, potassium metasilicate,
Examples include inorganic alkalis such as sodium orthosilicate and potassium orthosilicate. In addition, aqueous ammonia and organic alkalis include alkylamines, alkanolamines, etc. For example, alkylamines include monoethylamine, diethylamine, triethylamine, etc. Examples of alkanolamines include monoethanolamine, jetanolamine, and triethanolamine, and examples of alicyclic amines include morpholine. Furthermore, ethylene amines and propylene amines such as ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, pentaethylene hegisamine, and piperanzine can be used.
本発明において、(A)成分である一般式(Dで示され
る水溶性有機溶剤の配合皺が限定されるのは、80重量
%以上では、(B)成分である水溶性ポリアクリル酸が
沈殿してしまうため均一な組成物とならず、また20重
量%未満では、@離効果が低下するためと1組成物中の
水の割合が高くなり(B)成分である水溶性ポリアクリ
ル酸の溶解度が上がり組成物の粘度が高くなりすぎてし
まうためである。好ましくは30〜50重量%である。In the present invention, the compounding wrinkle of the water-soluble organic solvent represented by the general formula (D), which is the component (A), is limited because at 80% by weight or more, the water-soluble polyacrylic acid, which is the component (B), precipitates. If it is less than 20% by weight, the release effect will decrease and the proportion of water in one composition will increase, making it difficult to form a uniform composition. This is because the solubility increases and the viscosity of the composition becomes too high.Preferably it is 30 to 50% by weight.
(B)成分である水溶性ポリアクリル酸の配合量が限定
されるのは、5重量%以上では均一な組成物が得られず
水溶性ポリアクリル酸が沈殿してしまうためである。0
.1重量%以下では希釈時充分なる粘度が得られないた
めである。好ましくは0゜5〜3重1%である。The amount of the water-soluble polyacrylic acid, component (B), is limited because if it exceeds 5% by weight, a uniform composition cannot be obtained and the water-soluble polyacrylic acid will precipitate. 0
.. This is because if it is less than 1% by weight, sufficient viscosity cannot be obtained upon dilution. Preferably it is 0.5 to 3% by weight.
(C)成分である非イオン性界面活性剤の配合量が限定
されるのは、0.1重量%以下では希釈使用時の浸透、
潤滑効果が劣るため剥離残しの原因となる。5重量%以
上加えても効果に差はない。The amount of nonionic surfactant (C) component is limited because if it is less than 0.1% by weight, it will not penetrate well when used diluted.
The lubricating effect is poor, resulting in residual peeling. There is no difference in effect even if 5% by weight or more is added.
(D)成分である多価アルコールの配合量が限定される
のは、0.1重量%以下では充分なる保水効果が得られ
ず、20重量%以上加えても保水効果に差がないためで
ある。好ましくは2〜15重量%である。The amount of polyhydric alcohol, component (D), is limited because if it is less than 0.1% by weight, a sufficient water-retaining effect cannot be obtained, and if it is added more than 20% by weight, there is no difference in the water-retaining effect. be. Preferably it is 2 to 15% by weight.
(E)成分である無機および有機アルカリの配合量は1
組成物のPHがアルカリ性好ましくはP旧1〜13とな
るに必要な量である。 PI(I1以下では充分に樹脂
ワックス膜を剥離できず、またPH13以上では組成物
の安定性に欠けてしまう、酸である成分(B)の水溶性
ポリアクリル酸(例えば先に挙げたハイビスワコ−10
3では0.2重量%濃度水溶液においてPH1前後を示
す)の種類と配合量並びに成分(E)の種類による塩基
性の強弱により成分(E)の無機および有機アルカリの
配合量がきまる。The amount of inorganic and organic alkali (E) component is 1
The amount is necessary so that the pH of the composition becomes alkaline, preferably 1 to 13. If the PI (I) is below I1, the resin wax film cannot be removed sufficiently, and if the pH is above 13, the composition will lack stability. 10
The amount of the inorganic and organic alkalis of component (E) to be blended is determined by the type and amount of Component (E) (in which pH is around 1 in a 0.2% concentration aqueous solution) and the strength of basicity depending on the type of component (E).
成分(E)なる無機および有機アルカリの役割は二つに
分けることができる。すなわち組成物の使用時に水希釈
により粘度を発現させるために成分(B)なる水溶性ポ
リアクリル酸の中和剤としての(@きと、中和以上のす
なわち遊離したアルカリにより樹脂ワックス膜を溶解せ
しめる役割である。The roles of the inorganic and organic alkali components (E) can be divided into two. In other words, in order to develop the viscosity by diluting with water when the composition is used, the resin wax film is dissolved with an alkali that is more than neutralized, that is, freed, as a neutralizing agent for water-soluble polyacrylic acid, which is component (B). It is a role to encourage people.
成分(B)なる水溶性ポリアクリル酸を中和せしめる(
E)なる無機および有機アルカリは、水溶性ポリアクリ
ル酸を凝集沈殿させてしまう二価金属の水酸化物、1i
′酸塩、リン酸塩、およびケイ酸塩などであってはなら
ない、更に同様の理由からエチレンジアミンに代表され
るポリエチレンポリアミン類も主たる中和剤としては使
用できない、ただし用いようとするポリエチレンポリア
ミン類よりも強い塩基性の成分(IE)なる無機および
有機アルカリ、例えば水酸化ナトリウムなどで成分(B
)なる水溶性ポリアクリル酸を中和(好ましくはPH7
゜5以上)した後であれば加えることができる。樹脂ワ
ックス艶出し剤の主成分である金属架橋型アクリル樹脂
のアルカリ水溶液可溶性に基づく樹脂ワックス膜の剥離
のためには、無機アルカリだけでアルカリ性とした剥離
剤組成物よりも中和量以上のすなわち遊離した有機アル
カリでアルカリ性とした組成物の方が非常に効果的であ
る。したがって、本発明組成物では成分(E)の無機お
よび有機アルカリのうち有機アルカリ成分が、成分(B
)の水溶性ポリアクリル酸の中和に全て消費されないで
、遊離の状態で組成物中に存在することが不可欠である
。剥離作業のm墳を考えれば、揮発性のアンモニアやア
ルキルアミンよりも揮発しにくいモノエタノールアミン
に代表されるアルカノールアミンやポリエチレンアミン
類の使用が好ましい。Neutralize the water-soluble polyacrylic acid that is component (B) (
E) Inorganic and organic alkalis are divalent metal hydroxides, which cause water-soluble polyacrylic acid to coagulate and precipitate.
It must not be an acid salt, phosphate, or silicate, and for the same reason, polyethylene polyamines such as ethylene diamine cannot be used as the main neutralizing agent. Component (IE) with inorganic and organic alkalis, such as sodium hydroxide, is more strongly basic than component (IE).
) to neutralize the water-soluble polyacrylic acid (preferably at pH 7).
It can be added after 5° or more). In order to remove the resin wax film based on the solubility of the metal crosslinked acrylic resin, which is the main component of the resin wax polish, in an aqueous alkali solution, it is necessary to Compositions made alkaline with free organic alkali are much more effective. Therefore, in the composition of the present invention, among the inorganic and organic alkalis of component (E), the organic alkali component is
) is present in the composition in free form, without being completely consumed in the neutralization of the water-soluble polyacrylic acid. Considering the importance of peeling work, it is preferable to use alkanolamines such as monoethanolamine and polyethyleneamines, which are less volatile than volatile ammonia and alkylamines.
また本発明組成物は、必要に応じて香料2色゛素、防腐
剤、防錆剤などを含有することができる0本発明組成物
の製造方法は、ゆるやかに攪拌された成分(A)なる水
溶性有機溶剤中に成分(B)なる水溶性ポリアクリル酸
を徐々に加え均一に分散させる0次いで成分(C)なる
非イオン性界面活性剤、成分(D)なる多価アルコール
、さらに水(F)を加え攪拌して均一にする。最後に成
分(E)なる無機および有機アルカリをhOえ攪拌する
ことにより得られる。In addition, the composition of the present invention may contain a fragrance pigment, a preservative, a rust preventive agent, etc. as required. Component (B), a water-soluble polyacrylic acid, is gradually added to a water-soluble organic solvent and dispersed uniformly.Next, component (C) is a nonionic surfactant, component (D) is a polyhydric alcohol, and water ( Add F) and stir to make it homogeneous. Finally, component (E), an inorganic and organic alkali, is obtained by stirring in HO.
[発明の効果1
この様にして得られる本発明組成物は、室温において5
0〜200cpsの容易な原動性を示しこの状態で運搬
、保管をし、使用時に2〜5倍に水で希釈し攪拌により
容易に100.000以上〜5,0OOcpsのゲル−
水あめ状とすることができる。[Effect of the invention 1 The composition of the present invention obtained in this way has a
It exhibits easy motive power of 0 to 200 cps, and can be transported and stored in this state, and when used, diluted 2 to 5 times with water and stirred to easily produce a gel of 100,000 or more to 5,000 cps.
It can be made into starch syrup.
このように、本発明の剥離剤は使用時の水希釈により粘
度を増加させることができるので、従来剥離剤を保持さ
せることの難しかった現場においても使用を可能とし、
さらに樹脂ワックス膜に均一に充分厚く塗布可能とする
ことで最大限に化学的効果を発揮せしめ、かつ乾燥をお
さえることにより、除去しようとする樹脂ワーIクス膜
との接触有幼時間を長くすることによりポリシャー不要
とすることができる。As described above, the viscosity of the release agent of the present invention can be increased by diluting it with water during use, so it can be used even in sites where it was difficult to retain the release agent in the past.
Furthermore, by making it possible to coat the resin wax film uniformly and thickly, it maximizes the chemical effect, and by suppressing drying, the contact time with the resin work film to be removed is extended. This makes it possible to eliminate the need for a polisher.
本発明の剥離剤による剥離作業は、水希釈により増粘せ
しめた後モツプ等を床、階段などに厚く塗布し5分程放
置後に、スクイジーあるいは吸水バキュームにより回収
した後水ぶきを行なうだけで作業を完了できる。したが
って従来の剥離作業は通常廊下、ロビーにおいて5名(
剥離剤塗布に1名、ポリラシャ一作業に1名、汚水回収
に1名、水拭きに2名)で行なわれていたが、本発明組
成物の剥離剤を使用することにより同等の作業処理能力
をポリラシャ−不要により4名に省力化できた9作業難
易度の高い事務室等の種々のものが置かれた入り組んだ
場所での剥離作業は、ポリラシャ−不要に加えポリラシ
ャ−を使用できず手作業による研磨にたよっていた部分
の剥離作業を簡素化することができたので、大幅に作業
処理量が増え省力化できた。さらに最も作業難易度の高
い段階では手作業による研磨作業を必要としないため格
別に作業能率を改善できた。また特殊な現場であるフリ
ーアクセスフロア−にも対応できた。To remove the product using the remover of the present invention, simply thicken it by diluting it with water, apply it thickly to floors, stairs, etc., leave it for about 5 minutes, collect it with a squeegee or water vacuum, and then spray it with water. Able to complete work. Therefore, conventional stripping work is usually performed by five people (
Previously, it required one person to apply the remover, one person to apply the polisher, one person to collect the waste water, and two people to wipe the water, but by using the remover of the present invention, the same work processing capacity can be achieved. 9 Work can be reduced to 4 people by eliminating the need for PolyLasher 9. Peeling work in complex areas with various objects such as offices, which is highly difficult, requires no PolyLasher, and it is not possible to use PolyLasher by hand. Since we were able to simplify the peeling work of parts that previously relied on manual polishing, we were able to significantly increase the throughput and save labor. Furthermore, because manual polishing work is not required at the most difficult stage, work efficiency has been significantly improved. We were also able to accommodate the special site of a raised floor.
[実施例] 実施例を挙げて本発明の特徴について例証する。[Example] Examples are given to illustrate the features of the present invention.
表−1(7)I 、II、[、EV、Vl−1木Raの
71施例であり、■は比較例を示す。Table 1 (7) 71 examples of I, II, [, EV, Vl-1 tree Ra, ■ indicates a comparative example.
(以下余白)
表−1実施例・比較例(数値は重量%である)*1 ハ
イビスワコ−103(和光純薬工業株製、商品名)比較
例■は比較例であり、アルカリ性ではなく中性である。(Leaving space below) Table 1 Examples/Comparative Examples (The values are in weight%) It is.
表−1に示す実施例工、■、m、rv、v及び比較例■
、更に市販の一般的剥離剤を比較例■とし、次に示す方
法で剥離試験を行った。Example works, ■, m, rv, v and comparative example ■ shown in Table-1
Furthermore, a commercially available general peeling agent was used as Comparative Example (2), and a peeling test was conducted using the following method.
・′J4離試験
(剥離試験片の作成)
25%の不揮発分を有する樹脂ワックスを5X l 5
c■黒色のビニー゛ルアスベストタイルに5回ハケで均
一に重ね塗りし24111i+間室温で放置した後、促
進条件として38±2℃に保った恒温槽中に6時間放置
した。その後常温の蒸留水に浸漬して1時間ゆるやかに
撹拌した。水中よりタイルを取りだし38±2℃の恒温
槽中に18時間放置したものを剥離試験片とした。ここ
での試験片の促進条件は日本フロアーボリッシュ工業会
規格−除去性−に準じた。・'J4 release test (preparation of peel test piece) Resin wax with 25% non-volatile content 5X l 5
c) It was coated uniformly on a black vinyl asbestos tile 5 times with a brush and left at room temperature for 24111+ minutes, and then left in a constant temperature bath kept at 38±2° C. for 6 hours as an acceleration condition. Thereafter, it was immersed in distilled water at room temperature and gently stirred for 1 hour. A tile was taken out of the water and left in a constant temperature bath at 38±2° C. for 18 hours, which was used as a peel test piece. The acceleration conditions for the test piece here were in accordance with the Japan Floor Borish Industry Association standards - removability.
(試験方法)
先の促進条件下に放置した剥離試験片上に20±2℃に
保った表−1の実施例I 、 工I 、 III 。(Test Method) Examples I, I, and III of Table 1 were kept at 20±2°C on peel test pieces left under the accelerated conditions described above.
■、■及び比較例■、更に比較例■の2あるいは5倍各
水希釈液を厚さ3■膳程に均一に塗布した。1分、5分
経過後流木で充分すすぎ風乾し211#結果を目視にて
判定した。完全に剥離されたものをO1剥離残しのあっ
たものをΔ、はとんど′Asされなかったものを×とし
て評価した。2, 2, Comparative Example 2, and 2 or 5 times diluted solutions of Comparative Example 2 with water were uniformly applied to a thickness of about 3 mm. After 1 minute and 5 minutes, the sample was thoroughly rinsed with driftwood and air-dried, and the 211# result was visually judged. Those that were completely peeled off were evaluated as Δ, those that had some O1 peeled off, and those that were not completely peeled off were evaluated as ×.
表−2に剥離試験結果と各実施例の性状ならびに各実施
例の水希釈時における粘度を示した。Table 2 shows the peel test results, the properties of each example, and the viscosity of each example when diluted with water.
(以下余白)
表−2剥離試験結果、組成物性状1組成物の木箱釈時粘
(粘度はcps)実施例I、II、III、rV、V、
比較例■、vnは10分を経過しても乾燥部分を生じる
ことはなかまた。(Left below) Table 2 Peel test results, Composition properties 1 Composition viscosity when exposed to wooden box (viscosity is cps) Examples I, II, III, rV, V,
Comparative Examples ■ and vn did not show any dry areas even after 10 minutes.
しかし比較例■は試験片上に保持させることができず流
れ落ち、2分後には乾燥部分を生じ始めその部分は剥離
残しとなった。比較例■の剥離試験結果の()は、試験
片をそれぞれの剥離剤希釈液を入れたビーカーに浸清し
同様に試験した結果である。However, Comparative Example (3) could not be held on the test piece and ran off, and after 2 minutes, dry areas began to appear and those areas remained peeled. The numbers in parentheses in the peel test results for Comparative Example ① are the results of a similar test in which the test piece was immersed in a beaker containing a diluted solution of the respective peeling agent.
Claims (1)
0〜80重量% R−O−(R′O)_nH・・・・( I ) (式中Rは炭素数1〜4のアルキル基、フェニル基ある
いはベンジル基を示し、R’はエチレン基又はプロピレ
ン基あるいはその両方、nは1〜3) (B)水溶性ポリアクリル酸 0.1〜5重量% (C)非イオン性界面活性剤 0.1〜5重量% (D)多価アルコール 0.1〜20重量% (E)無機もしくは有機アルカリ 1〜15重量% (F)水 35〜75重量% からなりアルカリ性を示すことを特徴とする樹脂ワック
ス膜剥離剤組成物。[Claims] (A) Water-soluble organic solvent 2 represented by the following general formula (I)
0 to 80% by weight R-O-(R'O)_nH...(I) (In the formula, R represents an alkyl group having 1 to 4 carbon atoms, a phenyl group, or a benzyl group, and R' represents an ethylene group or Propylene group or both, n is 1 to 3) (B) Water-soluble polyacrylic acid 0.1 to 5% by weight (C) Nonionic surfactant 0.1 to 5% by weight (D) Polyhydric alcohol 0 .1 to 20% by weight (E) 1 to 15% by weight of an inorganic or organic alkali and (F) 35 to 75% by weight of water, and is characterized by exhibiting alkalinity.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62054916A JP2544919B2 (en) | 1987-03-10 | 1987-03-10 | Resin wax film remover composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62054916A JP2544919B2 (en) | 1987-03-10 | 1987-03-10 | Resin wax film remover composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63221179A true JPS63221179A (en) | 1988-09-14 |
JP2544919B2 JP2544919B2 (en) | 1996-10-16 |
Family
ID=12983931
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62054916A Expired - Lifetime JP2544919B2 (en) | 1987-03-10 | 1987-03-10 | Resin wax film remover composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2544919B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995014061A1 (en) * | 1993-11-15 | 1995-05-26 | Irvin Barnett | Lead paint remover |
JP2000230154A (en) * | 1998-12-11 | 2000-08-22 | Yuho Chem Kk | Composition for recovering floor polish and method for recovery |
KR100401724B1 (en) * | 2000-12-05 | 2003-10-17 | 기아자동차주식회사 | Chemical method for removing paint film on plastic resin using iso-propyl alcohol |
JP2004237191A (en) * | 2003-02-05 | 2004-08-26 | Kenzaburo Sato | Method of washing family buddhist altar and buddhist instrument |
JP2008537037A (en) * | 2005-04-15 | 2008-09-11 | イーコラブ インコーポレイティド | Floor coating stripping composition that thickens after dilution and stripping method |
JP2020132874A (en) * | 2019-02-13 | 2020-08-31 | スズカファイン株式会社 | Method of removing existing coating |
-
1987
- 1987-03-10 JP JP62054916A patent/JP2544919B2/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995014061A1 (en) * | 1993-11-15 | 1995-05-26 | Irvin Barnett | Lead paint remover |
JP2000230154A (en) * | 1998-12-11 | 2000-08-22 | Yuho Chem Kk | Composition for recovering floor polish and method for recovery |
KR100401724B1 (en) * | 2000-12-05 | 2003-10-17 | 기아자동차주식회사 | Chemical method for removing paint film on plastic resin using iso-propyl alcohol |
JP2004237191A (en) * | 2003-02-05 | 2004-08-26 | Kenzaburo Sato | Method of washing family buddhist altar and buddhist instrument |
JP2008537037A (en) * | 2005-04-15 | 2008-09-11 | イーコラブ インコーポレイティド | Floor coating stripping composition that thickens after dilution and stripping method |
JP2020132874A (en) * | 2019-02-13 | 2020-08-31 | スズカファイン株式会社 | Method of removing existing coating |
Also Published As
Publication number | Publication date |
---|---|
JP2544919B2 (en) | 1996-10-16 |
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