JPS62189B2 - - Google Patents
Info
- Publication number
- JPS62189B2 JPS62189B2 JP11897481A JP11897481A JPS62189B2 JP S62189 B2 JPS62189 B2 JP S62189B2 JP 11897481 A JP11897481 A JP 11897481A JP 11897481 A JP11897481 A JP 11897481A JP S62189 B2 JPS62189 B2 JP S62189B2
- Authority
- JP
- Japan
- Prior art keywords
- alkali
- weight
- inorganic
- silicate
- calcium
- 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
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 18
- 239000002245 particle Substances 0.000 claims description 12
- 239000003513 alkali Substances 0.000 claims description 11
- 239000003365 glass fiber Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000011256 inorganic filler Substances 0.000 claims description 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 10
- 239000008199 coating composition Substances 0.000 claims description 9
- 239000000378 calcium silicate Substances 0.000 claims description 5
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 5
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 claims description 5
- 235000010261 calcium sulphite Nutrition 0.000 claims description 5
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 4
- FAYYUXPSKDFLEC-UHFFFAOYSA-L calcium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [Ca+2].[O-]S([O-])(=O)=S FAYYUXPSKDFLEC-UHFFFAOYSA-L 0.000 claims description 3
- 239000000203 mixture Substances 0.000 description 13
- 239000003973 paint Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000010454 slate Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000005909 Kieselgur Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229920006184 cellulose methylcellulose Polymers 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000006253 efflorescence Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- -1 shirasu balloons Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Description
本発明は無機質塗料組成物に関しケイ酸アルカ
リ水溶液、和水ケイ酸アルカリと亜硫酸カルシウ
ムおよび/またはチオ硫酸カルシウム、ケイ酸カ
ルシウムと耐アルカリ性ガラス繊維とよりなる自
己硬化性の無機質塗料に関する。
従来ケイ酸アルカリ水溶液を結合剤とした無機
質塗料組成物は多数提案されているが、その大部
分は加熱処理を必要とし一般建築用外装材に用い
る場合、現場施工が困難な制限がある。本出願人
は先に耐水性が良好でかつアルカリ炭酸塩の滲出
が認められない硬化剤を含みこれに無機質充填剤
および顔料等を添加した常温硬化性の無機質塗料
組成物について提案した(特公昭54−66925号)。
この組成物は充填剤を種々変化させることによ
り一般建築用内外装材、隧道および地下道内装
剤、さらに接着剤等にも利用されるが系全体が不
燃無煙性の完全無機質であるため、反応硬化時の
乾燥収縮によるクラツクの発生はある程度避ける
ことができない。そのため塗料として各種用途に
応じたテクスチヤーを得るためには充填剤の粒度
を選択して亀裂を最小限に抑える等の措置を必要
とする。又化粧的効果のある塗膜を得るためには
種々の粒度の充填剤の併用が考えられるが少くと
も塗膜厚みが1〜2mmになればクラツクの発生が
避けられないという問題点があつた。
本発明の目的はこれらの欠点を除去し高度の塗
膜硬度と圧縮強度および接着強度等の大幅な向上
を与え且つ硬化時のクラツクを生じない無機質塗
料組成物を提供することである。
すなわち本発明は(A)ケイ酸アルカリ、(B)該ケイ
酸アルカリ固形分含量に対し合計で30〜300重量
%の亜硫酸カルシウムおよび/またはチオ硫酸カ
ルシウムとケイ酸カルシウムとよりなる硬化剤、
(C)粒径2mm以下の無機質充填剤、上記(A)〜(C)成分
の合計量に対し5〜50重量%の長さ50〜300μの
耐アルカリ性ガラス繊維を含有することを特徴と
する無機質塗料組成物である。
本発明に用いられる(A)成分のケイ酸アルカリと
してはナトリウム、カリウム、リチウムの如きア
ルカリ金属ケイ酸塩がよくSiO2/M2O(Mはア
ルカリ金属)モル比が1.5〜4.5の水溶液(濃度10
〜50重量%)あるいは水分10〜30重量%好ましく
は15〜25重量%を含む粉末状の和水ケイ酸アルカ
リが使用できる。和水ケイ酸アルカリとは無水ケ
イ酸アルカリから液状ケイ酸アルカリに移行する
際の中間物として得られるもので水分が10重量%
未満では水に対する溶解速度が遅く30重量%をこ
えると粉末の粘着性が大きくてブロツキングを起
し易い。また粉末の粒径は硬化剤等との混合性の
点から、平均400μ以下のものが好ましい。また
(B)成分の硬化剤は必須成分であり、これらの欠除
は硬化速度を著しく遅くし耐水性を悪化させまた
常温では硬化不良を起すため現場施工性が無い。
他に補助的な硬化剤として強度を向上させるため
に酸化亜鉛を併用してもよい。以上の硬化剤の配
合量が(A)成分のケイ酸アルカリ固形分含量に対し
30重量%未満では硬化不良を起し接着強度および
耐水性が著しく低下し白華現象を生ずる。また
300重量%をこえると可使時間が著しく短くなり
作業性が悪化する。本発明に用いられる(C)成分の
無機質充填剤としてはケイ砂、クレー、炭酸カル
シウム、タルク、ベントナイト、ケイソウ土、カ
オリン、パーライト、シラスバルーン、ヒル石粉
末、ガラスビーズ等があり粒度は用途に応じて適
当な粒径および粒度分布を持つた粉末を使用する
ことができる。配合量はケイ酸アルカリ固形分含
量に対し100〜1000重量%である。
本発明に使用される耐アルカリ性ガラス繊維の
長さ、形状は50μ〜300μ、好ましくは100〜200
μの長さを有する粉末状または綿状のものであ
る。繊維の長さが300μをこえると、混合時の分
散が悪くなるばかりでなく得られた塗膜の表面に
繊維が部分的に露出し意匠性が損われる。また繊
維の長さが50μ未満の場合は、クラツク防止の機
能が低下し無機質充填剤と同様になる。配合量と
しては上記(A)〜(C)成分の合計量に対して5〜50重
量%で良好な効果が得られる。50重量%をこえる
と系が増粘し取扱いが困難となる。その他本発明
組成物には増粘剤としてメチルセルローズ、
CMC、ポリアクリル酸、ポリアクリル酸ソーダ
等を配合して適度な粘性を付与することにより作
業性を改善しまた塗料組成物の沈降防止を図るこ
とも可能である。
本発明組成物を製造するには常温硬化性である
ため耐アルカリ性ガラス繊維はあらかじめ硬化
剤、充填剤等と混合しておき使用時にケイ酸アル
カリと混合する方法が好ましい。また従来ガラス
繊維で行われているカツプリング剤調整用として
のシラン処理、クロム処理を施しても塗膜に悪影
響を与えない。施用に際しては任意のコーテイン
グ手段、たとえば吹付け、ローラー塗り、コテ塗
り等を採用できる。また本発明塗料組成物の適用
される基材としては石綿、スレート板、パルプセ
メント板、PC板、ALC板、合板等各種のものが
挙げられる。
本発明塗料組成物はケイ酸アルカリの硬化剤と
して亜硫酸カルシウム、ケイ酸カルシウムを選択
することにより適切なポツトライフと良好な耐水
性を有するとともに耐アルカリ性ガラス繊維を含
有せしめることにより無機質塗料特有の欠点であ
つたクラツクの発生防止に著効がある。すなわち
従来品においてはクラツク防止のために使用され
る無機質充填剤の粒径が制限され且つ1〜2mm厚
みの塗膜を得るために2〜3回の仕上げ工程が必
要であつた。たとえばケイ砂の微粉末等粒径が約
30μ以下の無機充填剤を使用する場合、クラツク
発生防止のためには少くとも2回以上の仕上げを
要する。またたとえば寒氷石等のように粒径が1
〜2mmの無機質充填剤を使用する場合は仕上げ工
程を2回以上とした場合においても多数のクラツ
ク発生が認められる。しかるに本発明組成物のご
とくガラス繊維を混合含有せしめた場合は上記の
粒径を有する無機質充填剤を使用し1工程で1〜
2mm厚みの塗膜を形成せしめた際においても全く
クラツクの発生は認められない。さらに従来品に
比して得られた塗膜の硬度、圧縮強度、接着強度
等の諸物性も大巾な向上が認められる。すなわち
本発明塗料組成物によれば化粧材としての意匠性
が向上するばかりでなく工程が簡略化され、しか
もガラス繊維の混入により単位面積あたりの塗料
使用量が少くなる等経済的にも有利である。ま
た、特に基材としてALC板を用いる場合のよう
に表面層が脆弱で、しかも空気中の炭酸ガス、亜
硫酸ガス等によりアルカリが中和されて基材の中
性化が進行し表面層の劣化につながるような場
合、本発明塗料組成物を塗布しておくとこれが基
材の中まで浸透し表面層の強度を向上せしめると
共に外界からの酸性ガスに対して保護膜となり基
材の耐久性が増大する等の特徴を有している。以
下実施例により本発明の効果を説明する。各例中
の部、および%はそれぞれ重量部、重量%を表わ
す。
実施例1〜5、比較例1〜2
亜硫酸カルシウム40〜70部、ケイ酸カルシウム
15〜16部よりなる硬化剤と第1表に示す無機質充
填剤、顔料および耐アルカリ性ガラス繊維(商品
名ガラスカツトフアイバーFESS、富士フアイバ
ーガラス社製品)とを万能混合機で15分間混合し
てそれぞれ硬化系混合物を調整した。これにケイ
酸アルカリ水溶液または和水ケイ酸アルカリと水
を加えてラボミキサーで2分間混練りし無機質塗
料組成物を得た。また比較のため耐アルカリガラ
ス繊維を入れないほかは全く同様の無機質塗料組
成物を得た。これらの塗料物性の測定方法は次の
ごとくである。
(1) 耐ヒビ割れ試験−無機質塗料組成物を厚み3
mmの尺角石綿スレート板にスプレーガンを用い
て吹付け1回仕上げにて塗膜厚さ1〜2mmの塗
装板を作製する。吹付け仕上げ直後に室温(20
℃)で4〜5m/secの風を連続して6時間当
て塗膜のヒビ割れ状態を観察した。
耐ヒビ割れ試験の評価
◎;塗膜のヘアークラツク認められず
×;多数のヘアークラツク生成
(2) 圧縮強度−調合した無機質塗料組成物をポリ
塩化ビニール製の筒(直径25mm、高さ50mm)に
流し込み48時間後に脱型し25mm×50mmの成型体
を得た。これをさらに20℃にて48時間養生した
後、万能試験機(森試験機製作所製MU−2
型)を用いて圧縮強度を測定した。
(3) 付着強度−調合した無機質塗料組成物をスプ
レーガンを用いてモルタル板(70×70×20mm)
に吹付け室温(20℃)で5日間養生した後、万
能試験機を用いて測定した。
The present invention relates to an inorganic paint composition, and relates to a self-curing inorganic paint comprising an aqueous alkali silicate solution, a hydrous alkali silicate, calcium sulfite and/or calcium thiosulfate, calcium silicate, and alkali-resistant glass fiber. Many inorganic coating compositions using an aqueous alkali silicate solution as a binder have been proposed, but most of them require heat treatment, making it difficult to apply on-site when used as exterior materials for general construction. The applicant has previously proposed an inorganic paint composition that is curable at room temperature and contains a curing agent that exhibits good water resistance and does not cause leaching of alkali carbonates, and that contains an inorganic filler, pigment, etc. 54-66925). By changing the filler in various ways, this composition can be used as interior and exterior materials for general construction, interior materials for tunnels and underground passages, and even as adhesives, but since the entire system is completely inorganic and non-flammable and smokeless, it can be cured by reaction. Occurrence of cracks due to drying shrinkage cannot be avoided to some extent. Therefore, in order to obtain a texture suitable for various uses as a paint, it is necessary to take measures such as selecting the particle size of the filler to minimize cracks. In addition, in order to obtain a coating film with a cosmetic effect, it is possible to use fillers of various particle sizes in combination, but there is a problem that cracks are unavoidable when the coating thickness is at least 1 to 2 mm. . The object of the present invention is to eliminate these drawbacks and provide an inorganic coating composition that provides a high degree of coating film hardness and significantly improves compressive strength, adhesive strength, etc., and does not cause cracks during curing. That is, the present invention provides (A) an alkali silicate; (B) a curing agent comprising calcium sulfite and/or calcium thiosulfate and calcium silicate in a total amount of 30 to 300% by weight based on the solid content of the alkali silicate;
(C) An inorganic filler with a particle size of 2 mm or less, and an alkali-resistant glass fiber having a length of 50 to 300μ in an amount of 5 to 50% by weight based on the total amount of components (A) to (C) above. It is an inorganic paint composition. The alkali silicate of component (A) used in the present invention is preferably an alkali metal silicate such as sodium, potassium, or lithium. concentration 10
to 50% by weight) or a powdered alkali hydrohydrate silicate containing 10 to 30% by weight, preferably 15 to 25% by weight of moisture. Hydrated alkali silicate is obtained as an intermediate during the transition from anhydrous alkali silicate to liquid alkali silicate, and has a water content of 10% by weight.
If it is less than 30% by weight, the dissolution rate in water is slow, and if it exceeds 30% by weight, the powder becomes highly sticky and tends to cause blocking. In addition, the average particle size of the powder is preferably 400 μm or less from the viewpoint of miscibility with hardening agents and the like. Also
Component (B), the curing agent, is an essential component, and the absence of these significantly slows down the curing speed, deteriorates water resistance, and causes poor curing at room temperature, making it impossible to work on-site.
In addition, zinc oxide may be used in combination as an auxiliary hardening agent to improve strength. The amount of the above curing agent is based on the alkali silicate solid content of component (A).
If it is less than 30% by weight, curing failure will occur, resulting in a significant decrease in adhesive strength and water resistance, resulting in efflorescence. Also
If it exceeds 300% by weight, the pot life will be significantly shortened and workability will deteriorate. Inorganic fillers for component (C) used in the present invention include silica sand, clay, calcium carbonate, talc, bentonite, diatomaceous earth, kaolin, perlite, shirasu balloons, vermiculite powder, glass beads, etc., and the particle size varies depending on the application. Powders with suitable particle size and particle size distribution can be used accordingly. The blending amount is 100 to 1000% by weight based on the solid content of the alkali silicate. The length and shape of the alkali-resistant glass fiber used in the present invention are 50μ to 300μ, preferably 100 to 200μ.
It is powder-like or cotton-like with a length of μ. If the fiber length exceeds 300μ, not only will dispersion during mixing become poor, but the fibers will be partially exposed on the surface of the resulting coating film, impairing its design. If the length of the fibers is less than 50 μm, the anti-cracking function will be reduced and the result will be similar to that of an inorganic filler. Good effects can be obtained with a blending amount of 5 to 50% by weight based on the total amount of components (A) to (C). If it exceeds 50% by weight, the system will thicken and become difficult to handle. In addition, the composition of the present invention includes methylcellulose as a thickener,
By blending CMC, polyacrylic acid, sodium polyacrylate, etc. to impart appropriate viscosity, it is possible to improve workability and prevent sedimentation of the coating composition. In order to produce the composition of the present invention, it is preferable to mix the alkali-resistant glass fiber with a hardening agent, filler, etc. in advance and then mix it with an alkali silicate at the time of use, since it is curable at room temperature. Furthermore, even if glass fibers are subjected to silane treatment and chromium treatment for adjusting coupling agents, the paint film will not be adversely affected. For application, any coating method can be used, such as spraying, roller coating, troweling, etc. Further, various substrates to which the coating composition of the present invention can be applied include asbestos, slate boards, pulp cement boards, PC boards, ALC boards, plywood, and the like. The coating composition of the present invention has an appropriate pot life and good water resistance by selecting calcium sulfite and calcium silicate as hardening agents for alkali silicate, and also avoids the drawbacks peculiar to inorganic coatings by containing alkali-resistant glass fiber. It is highly effective in preventing the occurrence of hot cracks. That is, in conventional products, the particle size of the inorganic filler used to prevent cracks is limited, and two to three finishing steps are required to obtain a coating film with a thickness of 1 to 2 mm. For example, the particle size of fine powder of silica sand is approximately
When using an inorganic filler of 30μ or less, finishing is required at least twice to prevent cracks. Also, for example, the particle size is 1, such as cold stone.
When using an inorganic filler with a thickness of ~2 mm, a large number of cracks are observed even when the finishing process is performed two or more times. However, when glass fibers are mixed and contained as in the composition of the present invention, an inorganic filler having the above particle size is used, and 1- to
No cracks were observed even when a 2 mm thick coating was formed. Furthermore, the physical properties of the resulting coating film, such as hardness, compressive strength, and adhesive strength, are also significantly improved compared to conventional products. In other words, the coating composition of the present invention not only improves the design as a decorative material, but also simplifies the process, and is also economically advantageous, as the amount of paint used per unit area is reduced due to the inclusion of glass fibers. be. In addition, especially when the ALC board is used as a base material, the surface layer is fragile, and the alkali is neutralized by carbon dioxide gas, sulfur dioxide gas, etc. in the air, and the neutralization of the base material progresses, causing deterioration of the surface layer. In cases where the paint composition of the present invention is applied, it penetrates into the base material and improves the strength of the surface layer, and also acts as a protective film against acidic gases from the outside world, increasing the durability of the base material. It has characteristics such as increasing. The effects of the present invention will be explained below with reference to Examples. Parts and % in each example represent parts by weight and % by weight, respectively. Examples 1-5, Comparative Examples 1-2 40-70 parts of calcium sulfite, calcium silicate
A curing agent consisting of 15 to 16 parts, an inorganic filler shown in Table 1, a pigment, and an alkali-resistant glass fiber (product name: Glass Cut Fiber FESS, manufactured by Fuji Fiber Glass Co., Ltd.) were mixed for 15 minutes in a multipurpose mixer. A curing mixture was prepared. To this was added an aqueous alkali silicate solution or hydrous alkali silicate and water, and the mixture was kneaded for 2 minutes using a lab mixer to obtain an inorganic coating composition. For comparison, a completely similar inorganic coating composition was obtained except that no alkali-resistant glass fiber was added. The methods for measuring these physical properties of the paint are as follows. (1) Crack resistance test - inorganic paint composition with a thickness of 3
A coated plate with a coating thickness of 1 to 2 mm is produced by spraying once on a mm square asbestos slate plate using a spray gun. Immediately after spray finishing at room temperature (20
C) and was continuously exposed to wind at 4 to 5 m/sec for 6 hours to observe the state of cracks in the coating film. Evaluation of cracking resistance test ◎; Hair cracks in the paint film were not observed. After 48 hours, the mold was removed to obtain a 25 mm x 50 mm molded body. After further curing at 20°C for 48 hours, it was tested using a universal testing machine (MU-2 manufactured by Mori Shikenki Seisakusho).
The compressive strength was measured using a mold). (3) Adhesive strength - Apply the prepared inorganic paint composition to a mortar board (70 x 70 x 20 mm) using a spray gun.
After curing for 5 days at room temperature (20°C), measurements were taken using a universal testing machine.
【表】【table】
Claims (1)
〜300重量%の亜硫酸カルシウムおよび/また
はチオ硫酸カルシウムとケイ酸カルシウムとよ
りなる硬化剤 (C) 粒径2mm以下の無機質充填剤 上記(A)〜(C)成分の合計量に対し5〜50重量%の
長さ50〜300μの耐アルカリ性ガラス繊維を含有
することを特徴とする無機質塗料組成物。[Claims] 1 (A) Alkali silicate (B) 30 in total based on the solid content of the alkali silicate
Hardening agent (C) consisting of ~300% by weight of calcium sulfite and/or calcium thiosulfate and calcium silicate Inorganic filler with a particle size of 2 mm or less 5 to 50% by weight based on the total amount of components (A) to (C) above An inorganic coating composition characterized by containing alkali-resistant glass fibers having a length of 50 to 300μ in weight percent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11897481A JPS5819366A (en) | 1981-07-28 | 1981-07-28 | Inorganic coating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11897481A JPS5819366A (en) | 1981-07-28 | 1981-07-28 | Inorganic coating composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5819366A JPS5819366A (en) | 1983-02-04 |
JPS62189B2 true JPS62189B2 (en) | 1987-01-06 |
Family
ID=14749882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11897481A Granted JPS5819366A (en) | 1981-07-28 | 1981-07-28 | Inorganic coating composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5819366A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59211572A (en) * | 1983-05-17 | 1984-11-30 | Citizen Watch Co Ltd | Film formation of gold alloy |
JPS63314284A (en) * | 1987-06-17 | 1988-12-22 | Mitsubishi Heavy Ind Ltd | Heat-resistant anticorrosive coating film |
JP7129840B2 (en) * | 2018-07-27 | 2022-09-02 | 明星工業株式会社 | thermal insulation paint |
-
1981
- 1981-07-28 JP JP11897481A patent/JPS5819366A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5819366A (en) | 1983-02-04 |
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