JPH0349308B2 - - Google Patents
Info
- Publication number
- JPH0349308B2 JPH0349308B2 JP29195387A JP29195387A JPH0349308B2 JP H0349308 B2 JPH0349308 B2 JP H0349308B2 JP 29195387 A JP29195387 A JP 29195387A JP 29195387 A JP29195387 A JP 29195387A JP H0349308 B2 JPH0349308 B2 JP H0349308B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- weight
- water
- fiber
- viscosity
- 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
Links
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 30
- 239000000835 fiber Substances 0.000 claims description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 229920002125 Sokalan® Polymers 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 11
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 description 33
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- -1 pulp Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 10
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 8
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 7
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000010276 construction Methods 0.000 description 7
- 239000001768 carboxy methyl cellulose Substances 0.000 description 6
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 6
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 6
- 239000003292 glue Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000008399 tap water Substances 0.000 description 6
- 235000020679 tap water Nutrition 0.000 description 6
- 239000008187 granular material Substances 0.000 description 5
- RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 230000008719 thickening Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920006243 acrylic copolymer Polymers 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-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
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000011507 gypsum plaster Substances 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- LRMHFDNWKCSEQU-UHFFFAOYSA-N ethoxyethane;phenol Chemical compound CCOCC.OC1=CC=CC=C1 LRMHFDNWKCSEQU-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- On-Site Construction Work That Accompanies The Preparation And Application Of Concrete (AREA)
- Working Measures On Existing Buildindgs (AREA)
- Aftertreatments Of Artificial And Natural Stones (AREA)
- Paints Or Removers (AREA)
Description
本発明は室内に広く使用されている繊維壁の剥
離方法に関するものであり、詳しくは古い繊維壁
を簡単に剥離除去し、工期を著しく短縮せしめそ
の後の新しい繊維壁の塗工を有利に解決せしめる
繊維型剥離方法に関する。
一般に繊維壁はパルプなどの繊維質に京土、雲
母などの無機質と糊材としてカルボキシメチルセ
ルローズ(CMC)、酢酸−ビニール樹脂、酢ビー
アクリル共重合体、スチレン樹脂、アクリル系共
重合体などを混合し、水で混練し、壁などの仕上
材として住宅内装分野に広く使用されているもの
である。
繊維壁材は繊維質素材により次の4種類に区分
することができる。
綿状繊維を主原料とするもの。
木粉その他の粒状物を主原料とするもの。
糸状繊維を主原料とするもの。
有機繊維のほかに多量の無機材料の混入され
ているもの。
そして、これら繊維壁は次に示すような大きな
特徴を持つており、
糊が材料中に混入されているため、作業が簡
単。
作業性がすこぶるよいので施工能率が数倍も
上昇する。
熟練工でなくても施工ができる。
糊が腐敗しないためカビが生えない。
材料が豊富なため、豊富な色彩、柄がつくり
出せる。
品質が一定しているため、仕上りにムラがな
い。
その結果、京壁に代表されるような従来の天然
土壁に代つて新しい左官仕上材として木造住宅の
みならず、公団公社の住宅をはじめ学校、病院な
どにも広く施工されている。
一方、これら繊維壁が汚れたり、また老化した
りなどの理由、或いは他の必要性により模様替え
をする時、この壁材を取り除くことが一般に困難
であるので、大部分は上塗りをしているのが現状
である。こうすると、ひどい場合には柱よりも壁
が上に盛り上つてしまう。そのため古い繊維壁を
剥離するための薬剤が広く求められているが、現
在のところ適当な剥離剤は見出されていない。
本発明は良好な特性を有する繊維壁剥離剤を用
いて繊維壁を剥離する方法を提供することを目的
とするものであり、本発明者等は次のような研究
を重ねて本発明に到達したものである。
繊維壁を剥離除去するには、合成糊材を分解或
いは溶媒中に溶解、或いは分散せしめ、壁材の各
成分を壁に塗工される以前の状態に戻し、何らか
の方法で取り除く必要がある。そこで本発明者等
はその糊材をセロソルブ或はカルビトール中に溶
解、膨潤せしめ、更に水中に他の無機質成分とと
もに分散させて剥離することを検討した。しかし
ながら、古い繊維壁を除去する場合は、その壁が
少なくとも一層以上塗工されており、それを前記
システムで取り除くには大量の溶媒と水を垂直な
壁面に塗布しなければならない。このようなこと
は溶媒と水の混合物では極めて困難で、ほとんど
が垂れ落ちてしまうか、または揮散してしまい、
壁内部に滲みこんで内部の合成糊材を膨潤せしめ
ることはできない。
本発明者等は、この垂れ落ち問題を解消し、し
かも剥離効果を高めた繊維壁の剥離方法を提供す
ることを目的として、更に研究を重ねた結果、次
のような新規組成物が上記目的を達成しし得る
ことを見出した。
セロソルブ類、またはセロソルブ類および
カルビトール類
架橋型アクリル酸重合体
非イオン型界面活性剤
無機もしくは有機アルカリ
この組合物は懸濁状物であるが、該組成物
に必要に応じ水を加え、
セロソルブ類、またはセロソルブ類および
カルビトール類 30〜85重量%
架橋型アクリル酸重合体 0.6〜3重量%
非イオン界面活性剤 3.0〜6重量%
プロピレングライコール 0〜6重量%
無機もしくは有機アルカリ
0.15〜0.7重量%
水 0〜65重量%
からなる粘度100〜400CPSの組成物として保
管、運搬を行い、使用時に上記組成物と同量
ないし2倍の水で希釈して粘度を15000CPS以
上、好ましくは30000CPS以上に高めて剥離剤
として用いるのが最も好ましい方法であるとわ
かつた。この希釈後の増粘により垂れ落ちの問
題は解決され、ここに本発明の特徴があるので
ある。すなわち本発明は
セロソルブ類、またはセロソルブ類および
カルビトール類 30〜85重量%
架橋型アクリル酸重合体 0.6〜3重量%
非イオン界面活性剤 3.0〜6重量%
プロピレングライコール 0〜6重量%
無機もしくは有機アルカリ
0.15〜0.7重量%
水(好ましくは0〜46重量%)
0〜65重量%
からなる粘度100〜400CPSの繊維壁用剥離剤を
保管、運搬し、使用時に該剥離剤と同量ないし
2倍の水で希釈し粘度15000CSP以上に増粘せ
しめ、このものを繊維壁に塗布することからな
る、繊維壁の剥離方法に関するものである。
次に本発明に用いる剥離剤の各成分について、
その機能を説明すると共に、各成分の例を挙げ
る。
セロソルブ、カルビトール類はC.M.C.(カル
ボキシメチルセルロース)、スチレン−アクリ
ル共重合体、酢酸ビニル樹脂等、繊維質上塗材
のバインダー等の溶解剤である。セロソルブは
HOCH2CH2ORで表わされるエチレングリコ
ールのモノエーテルの総称で、Rはアルキル
基、中でもブチル、エチル、メチルが特に好ま
しい。カルビトール類は
HOCH2CH2OCH2CH2OCH2CH3で表わされる
ジエチレングリコールエチルエーテルの外、該
エーテル部分が、メチル、プロピル、イソプロ
ピルエーテルとなつているものをも包含する。
このものは任意成分で、セロソルブに対し、50
重量%以下、好ましくは20〜30重量%の割合で
加えることができる。セロソルブ、カルビトー
ルは水と相溶し、且つ揮発性が小さいので壁材
に使用されているバインダーを溶解、膨潤さ
せ、剥離剤使用時には存在する水の系に該膨潤
セロソルブ、カルビトールを分散させる効果が
大である。
これに対し、他の溶剤、例えばケトン、アル
コール等の水溶性極性溶媒は、これらバインダ
ーの溶解剤ではあるが、その揮発性等から当該
剥離剤の成分としたときに効果が極めて小さ
い。また非極性石油系溶媒(ベンジンなどのア
ルキル化合物、ベンゼン、トルエン、キシレン
など、及びそれらを含む芳香族系溶媒)或いは
塩素化溶媒では効果が全くない。
架橋型アクリル酸重合体はアクリル酸または
メタクリル酸類を、必要に応じ他の共重合性単
量体と共に、架橋剤の存在下で重合させて得ら
れる多分枝状に架橋された高分子主鎖に−
COOHを有する酸性の高分子電解質で(特開
昭49−130485号公報等参照)、合成高分子系増
粘剤として数種のものが市販されている。
架橋型アクリル酸重合体は多分枝状の分子構
造をもつた高分子物質で、側鎖に多くの解離基
が存在しているので、その水溶液は粒子の膨潤
とともに電気的斥力が働き、分子が伸長するこ
とによつて著るしい増粘現象を示す。このもの
の溶液は比較的低粘度であるが、これに適当な
アルカリを加えて中和するとイオン化が促され
て、分子が大きく伸長し溶液粘度は急上昇す
る。一般にその粘度は高分子物質と同様に濃度
が増えるに従つて増大する。
前記配合、の場合には、塩基で架橋型ア
クリル酸重合体が十分に中和されてなく、2〜
3倍の希釈によりアルカリ対イオンが増加し、
著しい粘度上昇がみられるものと考えられる。
こゝに致つて得られた塑性流動液は降伏値以
上の応力に対しては見かけ粘度が低下して流動
し、静置すると時間につれて粘度が回復し、使
用する上での大きな利点となる。
しかもこの増粘は浸透剤に影響を受け、アニ
オン系、カチオン系の活性剤では増粘がみられ
ない。浸透性にすぐれ、且つ増粘を阻害しない
活性剤は非イオン系のもののみである。
非イオン系界面活性剤は前記のように浸透
剤、かつ分離された壁材中の無機物質に対する
分散剤であり、ポリオキシエチレン系など親水
性の強く、浸透性のよい非イオン界面活性剤は
全て用いられるが、中でもポリオキシエチレン
アルキルフエノールエーテル類、特にポリオキ
シエチレン付加モル数6−14、アルキル基がオ
クチル又はノニル等のものや、ポリオキシエチ
レンソルビタンエーテル類が好ましく用いられ
る。
その配合量はソルベントに対して7%程度が
最も良く、配合量を規定以上に増加してもそれ
程良い結果は得られず、むしろ本発明に用いる
剥離剤のチキソトロピツク性を悪くする傾向に
ある。
プロピレングライコールは繊維壁中の合成糊
材に対する溶剤である。
無機または有機アルカリは前記の如く、架橋
型アクリル酸重合体に作用して溶液粘度を上昇
させる働きをするもので、NaOH、KOH、
NH4OH、モルホリン、モノエタノールアミン
等が用いられる。
粘度の高い液体は一般に浸透性に劣るが、本発
明に係わる剥離剤は壁面に塗工した場合、壁材に
含まれるアニオン性物質或いはアルカリ性無機塩
を溶かし、徐々に粘度低下が起り浸透力が改善さ
れ壁内部に滲みこみ壁材構造を破壊する。破壊さ
れた壁材構成物は該剥離剤中に溶解或いは分散す
る。この剥離剤と壁材構成物の混合物はダイラタ
ンシーを示し、流動性を失い垂直壁面にだれ落ち
ない状態となる。
古い繊維壁をこのような状態に変化させる剥離
方法として、本発明は新規なものであり、この状
態になつた古い壁を剥離するのは左官用のコテで
簡単に作業可能であり、而も、壁材構成物の飛散
もなく工法の容易さ、工期の短縮の点からみてす
ぐれた方法と云うことができる。
本発明に係わる組成物()の原液の温度によ
る粘度変化およびこの原液に同量ないし2倍の水
を加えて得られた2、3倍希釈液の粘度について
みた結果を次に示す。
組成物A
ブチルセロソルブ 47重量部
プロピレングリコール 3 〃
ノニフエニル系界面活性剤
エマルゲン911(花王石鹸(株)製、商品名) 3 〃
架橋型アクリル系共重合体
ハイビスワコーH−103 1 〃
(和光純薬工業(株)製、商品名)
苛性ソーダ水溶液25% 0.8 〃 水 45.2 〃
合計 100.0重量部
The present invention relates to a method for stripping fiber walls that is widely used indoors, and more specifically, it enables easy stripping and removal of old fiber walls, significantly shortening the construction period, and providing an advantageous solution to the subsequent application of new fiber walls. This invention relates to a fiber type peeling method. In general, fiber walls are made of fibers such as pulp, inorganic materials such as Kyoto clay and mica, and glue materials such as carboxymethyl cellulose (CMC), acetic acid-vinyl resin, vinegar-vinyl acrylic copolymer, styrene resin, and acrylic copolymer. It is mixed and kneaded with water, and is widely used in the field of residential interior decoration as a finishing material for walls, etc. Fiber wall materials can be classified into the following four types depending on the fibrous material. The main raw material is cotton fiber. Items whose main raw material is wood flour or other granular materials. The main raw material is filamentous fiber. Contains large amounts of inorganic materials in addition to organic fibers. These fiber walls have the following major characteristics: Because glue is mixed into the material, they are easy to work with. Workability is extremely good, increasing construction efficiency several times. It can be installed even if you are not a skilled worker. Because the glue does not rot, mold does not grow. Due to the abundance of materials, a wide variety of colors and patterns can be created. Because the quality is consistent, there is no unevenness in the finish. As a result, it has been widely used as a new plastering material in place of traditional natural clay walls such as Kyoto walls, not only in wooden houses but also in public corporation houses, schools, hospitals, etc. On the other hand, when these fiber walls become dirty or aged, or when redecorating due to other needs, it is generally difficult to remove this wall material, so most of them are coated with a top coat. is the current situation. If this is done, in severe cases the walls will rise above the pillars. Therefore, there is a wide demand for a chemical agent for peeling off old fiber walls, but no suitable peeling agent has been found so far. The present invention aims to provide a method for stripping fiber walls using a fiber wall stripping agent having good properties, and the present inventors have arrived at the present invention through repeated research as follows. This is what I did. In order to peel off and remove the fiber walls, it is necessary to decompose the synthetic glue material, dissolve or disperse it in a solvent, return each component of the wall material to its state before it was applied to the wall, and remove it by some method. Therefore, the present inventors have considered dissolving and swelling the adhesive in cellosolve or carbitol, and then dispersing it in water together with other inorganic components for peeling. However, when removing old fibrous walls, the walls are coated with at least one coat, which requires large amounts of solvent and water to be applied to the vertical walls in order to be removed by the system. This is extremely difficult to do with a mixture of solvent and water, as most of it drips or evaporates.
It cannot seep into the wall and swell the synthetic glue inside. The present inventors have conducted further research with the aim of solving this dripping problem and providing a method for peeling fiber walls that improves the peeling effect. As a result, the following new composition has been developed to meet the above objectives. We have discovered that it is possible to achieve this. Cellosolves, or cellosolves and carbitols Cross-linked acrylic acid polymer Non-ionic surfactant Inorganic or organic alkali This combination is a suspension, and if necessary, water is added to the composition to form a cellosolve. or cellosolves and carbitols 30-85% by weight Cross-linked acrylic acid polymer 0.6-3% by weight Nonionic surfactant 3.0-6% by weight Propylene glycol 0-6% by weight Inorganic or organic alkali
It is stored and transported as a composition with a viscosity of 100 to 400 CPS, consisting of 0.15 to 0.7% by weight of water and 0 to 65% by weight, and when used, it is diluted with the same amount to twice the amount of water as the above composition to bring the viscosity to 15,000 CPS or more, preferably. It has been found that the most preferable method is to increase the CPS to 30,000 CPS or higher and use it as a release agent. This increased viscosity after dilution solves the problem of dripping, which is a feature of the present invention. That is, the present invention comprises: Cellosolves or cellosolves and carbitols 30-85% by weight Cross-linked acrylic acid polymer 0.6-3% by weight Nonionic surfactant 3.0-6% by weight Propylene glycol 0-6% by weight Inorganic or organic alkali
0.15-0.7% by weight water (preferably 0-46% by weight)
A stripping agent for fiber walls consisting of 0 to 65% by weight with a viscosity of 100 to 400 CPS is stored and transported, and when used, diluted with the same amount or twice the amount of water as the stripping agent to increase the viscosity to 15,000 CSP or more. The present invention relates to a method for stripping a fiber wall, which method comprises applying a coating to the fiber wall. Next, regarding each component of the release agent used in the present invention,
We will explain its functions and give examples of each component. Cellosolve and carbitol are solubilizers for binders for fibrous topcoating materials such as CMC (carboxymethyl cellulose), styrene-acrylic copolymers, and vinyl acetate resins. Cellosolve is
A general term for ethylene glycol monoethers represented by HOCH 2 CH 2 OR, in which R is an alkyl group, with butyl, ethyl, and methyl being particularly preferred. Carbitols are
In addition to diethylene glycol ethyl ether represented by HOCH 2 CH 2 OCH 2 CH 2 OCH 2 CH 3 , it also includes those in which the ether moiety is methyl, propyl, or isopropyl ether.
This is an optional ingredient and is 50%
It can be added in a proportion of up to 20% by weight, preferably 20 to 30% by weight. Since cellosolve and carbitol are compatible with water and have low volatility, they dissolve and swell the binder used in wall materials, and when using a stripping agent, the swollen cellosolve and carbitol are dispersed in the water system that is present. The effect is great. On the other hand, other solvents, such as water-soluble polar solvents such as ketones and alcohols, are solvents for these binders, but their effectiveness is extremely small when used as a component of the stripping agent due to their volatility. Furthermore, nonpolar petroleum solvents (alkyl compounds such as benzine, benzene, toluene, xylene, etc., and aromatic solvents containing them) or chlorinated solvents have no effect at all. Cross-linked acrylic acid polymers are made by polymerizing acrylic acid or methacrylic acids in the presence of a cross-linking agent, along with other copolymerizable monomers if necessary, to form a multi-branched cross-linked polymer main chain. −
It is an acidic polymer electrolyte containing COOH (see JP-A-49-130485, etc.), and several types of synthetic polymer thickeners are commercially available. Cross-linked acrylic acid polymer is a polymer substance with a multi-branched molecular structure and has many dissociative groups in its side chains, so in its aqueous solution, electrical repulsion acts as the particles swell, causing the molecules to swell. It exhibits a remarkable thickening phenomenon upon stretching. A solution of this substance has a relatively low viscosity, but when an appropriate alkali is added to neutralize it, ionization is promoted, the molecules are greatly elongated, and the viscosity of the solution rises rapidly. Generally, the viscosity increases as the concentration increases, similar to polymeric substances. In the case of the above formulation, the crosslinked acrylic acid polymer is not sufficiently neutralized with the base, and the
A 3-fold dilution increases alkaline counterions,
It is thought that a significant increase in viscosity is observed. The plastic fluid liquid thus obtained flows with a lower apparent viscosity when subjected to stress greater than the yield value, and when left to stand still, the viscosity recovers over time, which is a great advantage in use. Moreover, this thickening is affected by the penetrating agent, and no thickening is seen with anionic or cationic active agents. The only active agents that have excellent permeability and do not inhibit thickening are nonionic ones. As mentioned above, nonionic surfactants are penetrants and dispersants for inorganic substances in separated wall materials. Nonionic surfactants with strong hydrophilicity and good permeability, such as polyoxyethylene, are All of them can be used, but among them, polyoxyethylene alkyl phenol ethers, particularly polyoxyethylene having an added mole number of 6 to 14 and an alkyl group such as octyl or nonyl, and polyoxyethylene sorbitan ethers are preferably used. The best blending amount is about 7% based on the solvent, and even if the blending amount is increased beyond the specified limit, good results will not be obtained, and the thixotropic properties of the stripping agent used in the present invention will tend to deteriorate. Propylene glycol is a solvent for the synthetic glue in the fiber walls. As mentioned above, inorganic or organic alkalis act on the crosslinked acrylic acid polymer to increase the solution viscosity, and include NaOH, KOH,
NH 4 OH, morpholine, monoethanolamine, etc. are used. Liquids with high viscosity generally have poor permeability, but when applied to a wall surface, the stripping agent according to the present invention dissolves anionic substances or alkaline inorganic salts contained in the wall material, gradually decreasing the viscosity and decreasing the permeability. It is improved and seeps into the wall and destroys the wall material structure. The destroyed wall material composition is dissolved or dispersed in the stripping agent. This mixture of release agent and wall material composition exhibits dilatancy and loses its fluidity so that it does not drip onto vertical wall surfaces. The present invention is a new peeling method for changing old fiber walls into this state, and peeling off old walls in this state can be easily done with a plasterer's trowel. This method can be said to be excellent in terms of ease of construction, shortening of construction period, and no scattering of wall material components. The results of changes in viscosity due to temperature of the stock solution of the composition () according to the present invention and the viscosity of a 2- to 3-fold diluted solution obtained by adding the same amount to twice as much water to this stock solution are shown below. Composition A Butyl cellosolve 47 parts by weight Propylene glycol 3 Noniphenyl surfactant Emulgen 911 (manufactured by Kao Soap Co., Ltd., trade name) 3 Crosslinked acrylic copolymer Hivis Wako H-103 1 (Wako Pure Chemical Industries, Ltd.) Co., Ltd., product name) Caustic soda aqueous solution 25% 0.8 Water 45.2 Total 100.0 parts by weight
【表】【table】
【表】
このものは下記の特性を示し、繊維壁剥離剤と
して望ましいものといえる。[Table] This product exhibits the following properties and can be said to be desirable as a fiber wall release agent.
【表】【table】
【表】
本発明の実施例に用いた組成物の具体例、およ
び本発明における剥離剤としての使用に当つて水
で希釈したときの粘度の変化、剥離剤として使用
したときの様子を、比較例に用いた組成物の具体
例と共に示す。
組成物1(実施例1用)
ポリオキシエチレンノニルフエノールエーテル
(商品名エマルゲン911花王石鹸(株)製) 4.0部
ブチルセロソルブ 45.0部
プロピレングライコール 4.0部
架橋型アクリル酸重合体
(ハイビスワコーH−103) 1.0部
25%NaOH水溶液 0.8部
水 45.2部
ポリオキシエチレンノニルフエノールエーテル
とブチルセロソルブを混合槽中で混和する。撹拌
を続けながら、この混合物中に架橋型アクリル酸
重合体を少しづつ加える。温度を50℃まで上げ不
溶性の粒がなくなるまで撹拌する。次にの混合物
を30〜40℃まで冷却し、プロピレングライコール
及び水を加え、更に25%NaOH溶液を一気に添
加し均一に混合する。
組成物2(実施例2用)
ポリオキシエチレンノニルフエノールエーテル
3.0部
ブチルセロソルブ 47.0部
架橋型アクリル酸重合体
(ハイビスワコーH−103) 1.4部
25%NaOH水溶液 1.0部
水 47.6部
以下組成物2〜5は組成物1の製法に準ずる。
組成物3(実施例3用)
ポリオキシエチレンオクチルフエノールエーテル
3.0部
ブチルセロソルブ 60.0部
架橋型アクリル酸重合体 3.0部
25%NaOH水溶液 1.8部
水 32.2部
組成物4(実施例4用)
ポリオキシエチレンノニルフエノールエーテル
(商品名エマルゲン911花王石鹸(株)製) 3.0部
ブチルセロソルブ 30.0部
架橋型アクリル酸重合体 1.0部
25%NaOH水溶液 1.5部
プロピレングリコール 4.0部
水 60.5部
組成物5(実施例5用)
ポリオキシエチレンソルビタンモノステアレート
(商品名トウイーン60花王石鹸(株)製) 3.0部
ブチルセロソルブ 40.0部
エチルカルビトール 5.0部
架橋型アクリル酸重合体 1.0部
プロピレングライユール 3.0部
25%アンモニア水 0.5部
水 37.5部
組成物6(比較例1用)
ソジウムオクチルスルフオサクシネート(花王ペ
レツクスOTP) 3.0部
ブチルセロソルブ 40.0部
プロピレングライコール 15.0部
水 42.0部
組成物6、7は組成物1の製法に準ずる。
組成物7(比較例2用)
ソジウムオクチスルフオサクシネート 3.0部
エチルセロソルブ 46.0部
プロピレングリコール 4.0部
架橋型アクリル酸重合体 1.0部
25%NaOH水溶液 0.8部
水 55.2部[Table] Comparison of specific examples of compositions used in the examples of the present invention, changes in viscosity when diluted with water when used as a release agent in the present invention, and appearance when used as a release agent. It is shown together with a specific example of the composition used in the example. Composition 1 (for Example 1) Polyoxyethylene nonylphenol ether (trade name Emulgen 911 manufactured by Kao Soap Co., Ltd.) 4.0 parts Butyl cellosolve 45.0 parts Propylene glycol 4.0 parts Cross-linked acrylic acid polymer (Hivis Wako H-103) 1.0 parts 25% NaOH aqueous solution 0.8 parts water 45.2 parts Mix polyoxyethylene nonylphenol ether and butyl cellosolve in a mixing tank. Add the crosslinked acrylic acid polymer little by little to this mixture while continuing to stir. Increase the temperature to 50°C and stir until there are no more insoluble particles. Next, the mixture is cooled to 30-40°C, propylene glycol and water are added, and then a 25% NaOH solution is added all at once and mixed uniformly. Composition 2 (for Example 2) Polyoxyethylene nonylphenol ether
3.0 parts Butyl cellosolve 47.0 parts Cross-linked acrylic acid polymer (Hibis Wako H-103) 1.4 parts 25% NaOH aqueous solution 1.0 parts Water 47.6 parts The following compositions 2 to 5 follow the manufacturing method of composition 1. Composition 3 (for Example 3) Polyoxyethylene octyl phenol ether
3.0 parts Butyl cellosolve 60.0 parts Cross-linked acrylic acid polymer 3.0 parts 25% NaOH aqueous solution 1.8 parts Water 32.2 parts Composition 4 (for Example 4) Polyoxyethylene nonyl phenol ether (trade name Emulgen 911 manufactured by Kao Soap Co., Ltd.) 3.0 parts Part Butyl cellosolve 30.0 parts Crosslinked acrylic acid polymer 1.0 parts 25% NaOH aqueous solution 1.5 parts Propylene glycol 4.0 parts Water 60.5 parts Composition 5 (for Example 5) Polyoxyethylene sorbitan monostearate (trade name Tween 60 Kao Soap Co., Ltd.) ) 3.0 parts Butyl cellosolve 40.0 parts Ethyl carbitol 5.0 parts Cross-linked acrylic acid polymer 1.0 parts Propylene grayul 3.0 parts 25% ammonia water 0.5 parts Water 37.5 parts Composition 6 (for Comparative Example 1) Sodium octylsulfosaccharide Nate (Kao Perex OTP) 3.0 parts Butyl Cellosolve 40.0 parts Propylene Glycol 15.0 parts Water 42.0 parts Compositions 6 and 7 follow the manufacturing method of Composition 1. Composition 7 (for Comparative Example 2) Sodium octisulfosuccinate 3.0 parts Ethyl cellosolve 46.0 parts Propylene glycol 4.0 parts Cross-linked acrylic acid polymer 1.0 parts 25% NaOH aqueous solution 0.8 parts Water 55.2 parts
【表】【table】
【表】
実施例1〜5及び比較例1、2
(1) 耐水性繊維壁材(GFWA)
軽量陶器造粒物 500部
有機無機質造粒物(着色) 600部
無機質発泡粒着色物 350部
軽量陶器造粒着色物 350部
CMC 60部
上記配合割合にて混合し、これに水道水2.2、
酢ビアクリル共重合エマルジヨン700部を加えて
混練りし、石膏プラスター下地にコテ塗りし、20
℃、65%の恒温、恒湿室にて1ケ月間、乾燥養生
した。
このものに、組成物1〜5の各組成物1部に水
道水2部を加えて希釈し、充分撹拌後1m/1m
厚程度に塗布し、30分間放置し、ケレン棒(スク
レーパー)にて除去したところ、簡単に除去でき
た(実施例1〜5)。また組成物6、7を用いて
同様の操作を行い(比較例1、2)、上記実施例
1〜5用の組成物1〜5を用いた場合と併せて、
その剥離の状態を表−4に示す。[Table] Examples 1 to 5 and Comparative Examples 1 and 2 (1) Water-resistant fiber wall material (GFWA) Lightweight ceramic granules 500 parts Organic-inorganic granules (colored) 600 parts Colored inorganic foam granules 350 parts Lightweight Pottery granulated colored material 350 parts CMC 60 parts Mix at the above mixing ratio, add 2.2 parts of tap water,
Add 700 parts of acetic acid biacrylic copolymer emulsion, mix, and apply with a trowel to the gypsum plaster base.
The samples were dried and cured for one month in a constant temperature and humidity room at 65% °C. This was diluted by adding 2 parts of tap water to 1 part of each of compositions 1 to 5, and after stirring thoroughly, 1 m/1 m
When it was applied to a thick layer, left for 30 minutes, and removed with a scraper, it was easily removed (Examples 1 to 5). In addition, similar operations were performed using Compositions 6 and 7 (Comparative Examples 1 and 2), and in addition to the case where Compositions 1 to 5 for Examples 1 to 5 were used,
The state of peeling is shown in Table 4.
【表】【table】
【表】
実施例 6
実施例1〜5と同じ壁材を石膏プラスター下地
に施工し、10年経過した壁面に、実施例1〜5用
の組成物1〜5の各1部に水道水2部を加え撹拌
後、450g/m2をコテ塗りし15分間放置し、ケレ
ン棒にて除去したところ、簡単に除去できた。塗
り厚は3〜4m/m程度あり、下地を損傷なく除
去できた。
なお、以下の繊維壁について同様の剥離試験を
行なつたところ、上記実施例1〜5及び6同様、
繊維質上壁部材を簡単に、また下地に損傷を与え
ることなく除去することができた。
(2) 砂壁(GFWA)
硅砂着色物 4900部
無機質軽量パウダー 20部
CMC 50部
アクリルスチレン共重合エマルシヨン 300部
(施工時 水道水 2000部)
(3) 高級じゆらく壁(GFA)(特許第1106701号)
アプルス着色物 1500部
白竜砕石 700部
CMC 80部
天然色土 350部
クレー 150部
添加助剤 40部
粉末パルプ 70部
酢ビエマルシヨン 100部
(施工時 水道水 3000部)
(4) 糸状繊維質上塗材(GF)
化繊特紡糸 80部
トリコツト繊維 160部
無機質発泡粒 50部
木粉 100部
アルミニウム 30部
合繊蒸着加工物 10部
CMC 90部
化繊撚糸 80部
(施工時 水道水 6500部)[Table] Example 6 The same wall materials as in Examples 1 to 5 were constructed on a gypsum plaster base, and on the wall surface after 10 years, 1 part each of Compositions 1 to 5 for Examples 1 to 5 and 2 parts of tap water were added. After stirring, 450 g/m 2 was applied with a trowel, left to stand for 15 minutes, and removed with a scraper, and it was easily removed. The coating thickness was about 3 to 4 m/m, and the base could be removed without damage. In addition, when similar peeling tests were conducted on the following fiber walls, similar to Examples 1 to 5 and 6 above,
The fibrous top wall member could be easily removed without damaging the underlying material. (2) Sand wall (GFWA) Colored silica sand 4900 parts Inorganic lightweight powder 20 parts CMC 50 parts Acrylic styrene copolymer emulsion 300 parts (Tap water at the time of construction 2000 parts) (3) High-grade Jiyuraku Wall (GFA) (Patent No. 1106701) No.) Apprus colored material 1500 parts Hakuryu crushed stone 700 parts CMC 80 parts Natural colored soil 350 parts Clay 150 parts Additives 40 parts Powder pulp 70 parts Vinyl acetate emulsion 100 parts (Tap water at the time of construction 3000 parts) (4) Filamentous fibrous top coating Materials (GF) Special spun synthetic yarn 80 parts Tricot fiber 160 parts Inorganic foam granules 50 parts Wood flour 100 parts Aluminum 30 parts Synthetic fiber vapor-deposited product 10 parts CMC 90 parts Synthetic fiber twisted yarn 80 parts (Tap water at the time of construction 6500 parts)
Claims (1)
びカルビトール類 30〜85重量% 架橋型アクリル酸重合体 0.6〜3重量% 非イオン界面活性剤 3.0〜6重量% プロピレングライコール 0〜6重量% 無機もしくは有機アルカリ 0.15〜0.7重量% 水 0〜65重量% からなる粘度100〜400CPSの繊維壁用剥離剤を保
管、運搬し、使用時に該剥離剤と同量ないし2倍
の水で希釈し粘度15000CPS以上に増粘せしめ、
このものを繊維壁に塗布することからなる、繊維
壁の剥離方法。[Claims] 1 Cellosolves, or cellosolves and carbitols 30 to 85% by weight Crosslinked acrylic acid polymer 0.6 to 3% by weight Nonionic surfactant 3.0 to 6% by weight Propylene glycol 0 to 6% by weight % Inorganic or organic alkali 0.15-0.7% by weight Water 0-65% by weight A fiber wall release agent with a viscosity of 100-400 CPS is stored and transported, and when used, it is diluted with the same amount or twice the amount of water as the release agent. Increased viscosity to over 15000 CPS,
A method for removing fiber walls, which consists of applying this material to the fiber walls.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29195387A JPS63194059A (en) | 1987-11-20 | 1987-11-20 | Method for releasing fiber wall |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29195387A JPS63194059A (en) | 1987-11-20 | 1987-11-20 | Method for releasing fiber wall |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63194059A JPS63194059A (en) | 1988-08-11 |
| JPH0349308B2 true JPH0349308B2 (en) | 1991-07-29 |
Family
ID=17775600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP29195387A Granted JPS63194059A (en) | 1987-11-20 | 1987-11-20 | Method for releasing fiber wall |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63194059A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6373712B2 (en) * | 2014-10-06 | 2018-08-15 | 憲史 河口 | Water-based paint cleaner |
-
1987
- 1987-11-20 JP JP29195387A patent/JPS63194059A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63194059A (en) | 1988-08-11 |
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