JPS60158269A - Film-forming composition - Google Patents
Film-forming compositionInfo
- Publication number
- JPS60158269A JPS60158269A JP1659084A JP1659084A JPS60158269A JP S60158269 A JPS60158269 A JP S60158269A JP 1659084 A JP1659084 A JP 1659084A JP 1659084 A JP1659084 A JP 1659084A JP S60158269 A JPS60158269 A JP S60158269A
- Authority
- JP
- Japan
- Prior art keywords
- alumina cement
- weight
- cement
- film
- gypsum
- 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.)
- Pending
Links
Landscapes
- Paints Or Removers (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、温度、湿度、下地の透水性等の外的条件に左
右されることなく、欠陥のない厚膜を比較的短時間に形
成させ得る高分子水分散体を含有する組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a polymer aqueous dispersion that can form a defect-free thick film in a relatively short period of time without being affected by external conditions such as temperature, humidity, and water permeability of the substrate. The present invention relates to a composition containing the following.
従来、建築構造物に対し保護、防水を目的に数matの
有機高分子の厚膜の施工がおこなわれておシ、反応型、
熱溶融型、高濃度溶液型などの材料が使われている。し
かしこれ等の材料は、混合が微妙であったシ、火気の使
用が必要だったシ、溶剤の揮発や臭気などの問題があり
、何にもまして湿潤面への施工が困難な欠点がある。水
系の材料、特に高分子水分散体はこれ迄も使用されてい
るが、常温での水の蒸気圧が有機溶媒のそれと比べて低
いため、重ね塗膜、塩凝固、セメントの混合等がおこな
われている。重ね塗膜の場合、夏4は未だしも、冬場は
蒸発速度の低下、水利速度の低下によシ能率が低下する
。塩凝固は冬場の塗膜形成能が低下することもあるが、
塩による鉄筋その他の腐蝕、吹付に伴う飛沫の害および
それを防止するための養生など問題がある。上記塗膜形
成法のうち、比較的問題の少ないのが、セメントの混合
である。ボルトランドセメントを用いた場合、水利硬化
と吸着水によシ自重の約40%の水を系より奪うとされ
ている。また、多価カチオンを生成し、また硬化過程で
表面積が約1000倍にもなシ、大きな表面自由エネμ
ギーを生成する。脱水と物理化学的作用によシ高分子水
分散体のコロイド状態を破壊し、厚膜形成を促進する。Conventionally, thick organic polymer films of several mats have been applied to architectural structures for the purpose of protection and waterproofing.
Materials such as heat-melting type and highly concentrated solution type are used. However, these materials have problems such as delicate mixing, the need to use fire, evaporation of solvents and odor, and above all, the disadvantage that it is difficult to apply to wet surfaces. . Water-based materials, especially water-based polymer dispersions, have been used for some time now, but because the vapor pressure of water at room temperature is lower than that of organic solvents, they are difficult to apply, such as overcoating, salt coagulation, and cement mixing. It is. In the case of multiple coatings, the efficiency decreases in the summer and in the winter due to a decrease in the rate of evaporation and a decrease in the rate of water use. Salt coagulation may reduce the ability to form a coating in winter, but
There are problems such as corrosion of reinforcing steel and other parts due to salt, damage caused by splashes caused by spraying, and curing to prevent this. Among the above coating film forming methods, the method with relatively few problems is the mixing of cement. When Bortland cement is used, it is said that about 40% of its own weight in water is taken away from the system through water hardening and adsorption. In addition, it generates polyvalent cations, and the surface area decreases approximately 1000 times during the curing process, resulting in a large surface free energy μ.
produce ghee. Dehydration and physicochemical actions destroy the colloidal state of the polymer water dispersion and promote thick film formation.
ポμトツンドセメントの欠点は上記水利反応の温度依存
性の他 。The disadvantages of potato cement include the above-mentioned temperature dependence of the water use reaction.
に水利硬化体の強度が大きく、塗膜の弾性率が著しく高
く、クラックが入シやすい致命的欠陥を有する。力μシ
ウムシリケートを主構成成分とするポルトランドセメン
トでは塗膜形成速度と塗膜の柔軟性を自由に調節するこ
とは不可能である。また、アルミナセメントのみを塗膜
形成促進剤として使うこともおこなわれている。この場
合は水利速度の温度依存性が比較的低いこと、水利硬化
物の結晶水が多い、すなわち脱水力が強いことの点で優
れている。しかし、アルミナセメントは急結性を有して
おり、特に夏鳩での配合物のポツトライプが保てない欠
点を有していも遅延剤の配合である程度の改善は可能で
あるが、完璧とは言い難い。従来のものは概してアルミ
ナセメントの速硬性を利用した処方になっておシ、塗膜
の弾性率は高くならざるを得ない。The strength of the water cured body is high, the elastic modulus of the coating film is extremely high, and it has the fatal defect of being prone to cracking. With Portland cement whose main component is μsium silicate, it is impossible to freely adjust the coating film formation rate and the flexibility of the coating film. Additionally, alumina cement alone has been used as a coating film formation accelerator. This case is advantageous in that the temperature dependence of the water utilization rate is relatively low and the water utilization cured product contains a large amount of crystallized water, that is, the dehydration power is strong. However, alumina cement has rapid setting properties, and even though it has the disadvantage of not being able to maintain the potstripe of the mixture especially in summer pigeons, it can be improved to some extent by adding a retarder, but it is not perfect. It's hard to say. Conventional formulations generally take advantage of the rapid hardening properties of alumina cement, and the elastic modulus of the coating film must be high.
本発明者等は上記のような欠点のない塗膜形成組成物に
ついて鋭意検討した結果、アルミナセメントとセラコラ
を併用し、これを高分子水分散体に特定量含有させると
温度、湿度、下地の透水性等の外的条件に何等左右され
ることなく、欠陥のない厚膜を比較的短時間に形成させ
ることができる組成物が得られることを知見し、この知
見に基づき、本発明を完成するに至った。The inventors of the present invention have conducted intensive studies on a coating film-forming composition that does not have the above-mentioned drawbacks, and have found that if alumina cement and Ceracola are used in combination and a specific amount of this is contained in a polymer aqueous dispersion, temperature, humidity, and substrate conditions can be improved. It was discovered that a composition capable of forming a defect-free thick film in a relatively short time can be obtained without being affected by external conditions such as water permeability, and based on this knowledge, the present invention was completed. I ended up doing it.
すなわち、本発明は、アμミナセメント、セツコウおよ
び高分子水分散体を含有し、アルミナセメントとセラコ
ラとの割合がアルミナセメント1重量部に対してセラコ
ラ約0.5〜7重量部で、l、アルミナセメントとセラ
コラの和が高分子水分散体100重量部に対し約10〜
200重量部である塗膜形成組成物である。That is, the present invention contains Amu-mina cement, Setsukou, and a polymer water dispersion, and the ratio of alumina cement and Ceracola is about 0.5 to 7 parts by weight of Ceracola to 1 part by weight of alumina cement, and 1 part by weight of Ceracola. , the sum of alumina cement and Ceracola is about 10 to 100 parts by weight of the polymer water dispersion.
200 parts by weight of the film forming composition.
本発明に用いられるアルミナセメンtとしては、たとえ
ばCa0A1203. Ca0a2A1203−12C
a0・7A1g03などの力μシウムアμミネートを主
成分とし、一部A1g03がFe2O3,CaOがMg
Oで置換されていてもよく、好適には市販の耐火・耐蝕
工事用のものがあげられる。Examples of alumina cement used in the present invention include Ca0A1203. Ca0a2A1203-12C
The main component is force μsium μ laminate such as a0・7A1g03, some A1g03 is Fe2O3, and CaO is Mg.
It may be substituted with O, and commercially available ones for fireproofing and corrosion-proofing construction are preferred.
本発明に用いられるセラコラとしては、たとえば無水、
半水、2水のいずれでもよいが、溶解度の点から2水セ
ツコウ、純度の点から化学セラコラが好ましい。Ceracola used in the present invention includes, for example, anhydrous,
Either half-water or di-water may be used, but di-hydrate is preferred from the viewpoint of solubility, and chemical Ceracola is preferred from the viewpoint of purity.
前述のアルミナセメントとセラコラを高分子水分散体に
含有させる。The alumina cement and Ceracola described above are contained in a polymer water dispersion.
その場合、アルミナセメントとセラコラとの割合がアル
ミナセメント1重量部に対してセラコラ約0.5〜7重
量部となるのが好ましく、アルミナセメントとセラコラ
の和が高分子水分散体100重量部に対して約10〜2
00重量部となるように加えられる。アルミナセメント
1重量部に対するセラコラの割合が0.5重量部未満で
は塗膜が硬くなる。7重量部を越えると乾燥性が充分で
ない。In that case, it is preferable that the ratio of alumina cement and Ceracola is about 0.5 to 7 parts by weight of Ceracola to 1 part by weight of alumina cement, and the sum of alumina cement and Ceracola is 100 parts by weight of the polymer water dispersion. About 10-2
00 parts by weight. If the ratio of Ceracola to 1 part by weight of alumina cement is less than 0.5 parts by weight, the coating film will become hard. If it exceeds 7 parts by weight, drying properties will not be sufficient.
マタ、アルミナセメントとセラコラの和が高分子水分散
体100重量部に対して10重量部未満では乾燥性が充
分でなく、200重量部を越えると塗膜が硬くなる。ア
ルミナセメントとセラ、コラはいずれも粉末状であるの
でこれらを予め混合しておいてもよく、あるいはそれら
を別々に高分子水分散体に添加してもよい。If the sum of alumina cement and Ceracola is less than 10 parts by weight based on 100 parts by weight of the water polymer dispersion, drying properties will not be sufficient, and if it exceeds 200 parts by weight, the coating will become hard. Since alumina cement, Cera, and Kola are all in powder form, they may be mixed in advance, or they may be added separately to the polymer water dispersion.
本発明に用いられる高分子水分散体としては乾燥によシ
造膜するものであれば如何なるものでもよく、たとえば
天然9合成ゴムラテックス、合成樹脂エマμジョン、ア
スファμトエマμジョンなどが好適である。これらの水
分散体は、アルミナセメントやセラコラとの混合安定性
が要求されるが、その混合安定性はたとえばポリオキシ
エチレンアμキpエーテμ、ポリオキシエチレンアμキ
μアリールエーテ/l/などのノニオン活性剤、アμキ
μ4級アンモニウム塩、アルキμフォスフオニウム塩、
アμキμスμフオニウム塩などの陽イオン活性剤を添加
することによシ得られる。The aqueous polymer dispersion used in the present invention may be of any type as long as it forms a film upon drying; for example, natural 9 synthetic rubber latex, synthetic resin emulsion, asphalt emulsion, etc. are suitable. be. These aqueous dispersions are required to have mixing stability with alumina cement and Ceracola, but the mixing stability is higher than that of, for example, polyoxyethylene aryl ether/l/l/ nonionic activators such as alkyl μ quaternary ammonium salts, alkyl μ phosphonium salts,
It can be obtained by adding a cationic activator such as an axophonium salt.
高分子水分散体の固形分濃度は約30〜75重量%、特
に約40〜65重量%程度が好ましい。The solid content concentration of the aqueous polymer dispersion is preferably about 30 to 75% by weight, particularly about 40 to 65% by weight.
アルミナセメント、セラコラおよび高分子水分散体を混
合することによシ木発明の塗膜形成組成物が得られる。By mixing alumina cement, Ceracola, and a polymeric water dispersion, the film-forming composition of Shiki's invention is obtained.
アルミナセメントおよびセラコラは施工直前に混合する
ことが好ましい。混合に際して、必要ならば組成物の流
動性を改善するために、たとえばポリビニルアμコーμ
、水溶性七μロース化合物などの水溶性増粘剤などを加
えても構わない。It is preferable to mix alumina cement and Ceracola immediately before construction. During mixing, if necessary, to improve the fluidity of the composition, e.g.
, a water-soluble thickener such as a water-soluble 7 μlose compound, etc. may be added.
このようにして得られる本発明の塗膜形成組成物は、建
築構造物の保護、防水目的で厚さ数−の膜厚となるよう
に施されるが、温度、湿度、下地の透水性等の外的条件
に何等左右されることなく、欠陥のない厚膜を比較的短
時間に形成することができる。The coating film-forming composition of the present invention obtained in this manner is applied to a film thickness of several times the thickness for the purpose of protecting and waterproofing architectural structures. Defect-free thick films can be formed in a relatively short time without being affected by external conditions.
以下実施例によシ本発明を更に具体的に説明する。The present invention will be explained in more detail below using Examples.
実施例1
アニオン/ノニオン系スチレンブタジェンゴムラテック
ス(OHX−02,武田薬品工業■製。Example 1 Anionic/nonionic styrene-butadiene rubber latex (OHX-02, manufactured by Takeda Pharmaceutical Company Ltd.).
固形分50重量%)およびノニオン系アスファルトエマ
ルジョン(アスゾーμA9日瀝化学製、固形分60重量
%)を重量比で30/100に混合、これの100重量
部に対しアルミナセメント(A120342重量%)と
2水セツコウとの混合物50重承部を加え、2mII+
厚に流延した結果を示す。Solid content: 50% by weight) and nonionic asphalt emulsion (Asso μA, manufactured by Nichirei Chemical Co., Ltd., solid content: 60% by weight) were mixed at a weight ratio of 30/100, and 100 parts by weight of this was mixed with alumina cement (A120342% by weight). Add 50 heavy bearing parts of the mixture with 2mII+
The results of thick casting are shown.
(注)硬化性は流延後24HRの指触乾燥で示す。(Note) Curability is shown as dry to the touch after 24 hours of casting.
O・・・乾燥終了
Δ・・・内部に未乾燥部残る
×・・・未乾燥部多い
皮膜伸びはアμミナセメント/セツコウ未添加物の伸び
を100とし
O・・・伸び保持率 50%以上
△・・・ 〃 10%以上50%未満
×−・・ ? 10%未満
アルミナセメントのみあるいはアルミナセメントが多い
配合(41,2)では、混合物の可使時間と得られた皮
膜の柔軟性が劣る。O...Drying complete Δ...Undried area remains inside ×...Large undried area The film elongation is based on the elongation of Amu Mina cement/Setsukou not added as 100. O...Elongation retention rate is 50% More than △...〃 10% or more and less than 50% ×-...? In formulations (41,2) containing only less than 10% alumina cement or with a large amount of alumina cement, the pot life of the mixture and the flexibility of the resulting film are poor.
これに対して本発明の実施例である轟3〜5のものは硬
化性と皮膜伸びの2点ですぐれていることが明らかでお
る。On the other hand, it is clear that Todoroki 3 to 5, which are Examples of the present invention, are superior in two points: curability and film elongation.
実施例2
実施例1に用いたのと同じ水分散体100重量部にアル
ミナセメント/2水セツコウ=174の混合物(硬化剤
)を添加し、実施例1と同様の試験をおこなった。比較
例はJ工S超早強セメント轟1 10 1000 90
0 Δく △ 02 40 1300 1500 0
0 03 60 1650 1900 0 0 04
100 600 450 00 05 140 130
0 1300 00 △較2 40 3800 510
0 σ込 △ △例3 60 調製中ゲμ化 −−−
(注)Al〜3.比較例1〜2は増粘剤を用い、&5〜
7は水を補充した。Example 2 A mixture (hardening agent) of alumina cement/dihydric acid = 174 was added to 100 parts by weight of the same water dispersion as used in Example 1, and the same test as in Example 1 was conducted. Comparative example is J Engineering S Super Early Strength Cement Todoroki 1 10 1000 90
0 Δku △ 02 40 1300 1500 0
0 03 60 1650 1900 0 0 04
100 600 450 00 05 140 130
0 1300 00 △ comparison 2 40 3800 510
0 σ included △ △Example 3 60 Geumization during preparation --- (Note) Al~3. Comparative Examples 1-2 used a thickener, &5-
7 refilled water.
、硬化性、皮膜伸びの表示は実施例1に同じ。, curability, and film elongation are the same as in Example 1.
実施例3
実施例1と同じ水分散体100重量部に対しアルミナセ
メント/2水セツコウ−171の混合物を50重量部加
えたものと、O/W型高固形分ゴムアスファμト防水材
との硬化性の比較をおこなった。Example 3 Curing of 100 parts by weight of the same aqueous dispersion as in Example 1 with 50 parts by weight of a mixture of alumina cement/di-water-171 added and an O/W type high solids rubber asphalt waterproofing material. A gender comparison was made.
(注)硬化性は2111111のものは流延後24HR
,5mmのものは48HR後の結果を示す。硬化性の表
示は実施例1に同じ。(Note) Curing property of 2111111 is 24HR after casting.
, 5 mm shows the results after 48 HR. The curability display is the same as in Example 1.
比較例では皮膜内部の硬化が遅い。これに対して本発明
の組成物は20℃および5℃での硬化性にすぐれている
ことが明らかである。In the comparative example, curing inside the film was slow. In contrast, it is clear that the composition of the present invention has excellent curability at 20°C and 5°C.
実施例4
各種水分散体100重量部に対し、アルミナセメント(
Al2O380,0重量%)/2水セッコウー1/3の
混合物を40重量部添加し硬化性および皮膜伸びを調べ
た。比較例としてJ工S超早強セ(注)皮膜伸びの0は
、アμミナセメント/セッコウ未添加物と殆んど同じ伸
びを示す。他 正の表示は実施例1に同じ。Example 4 Alumina cement (
40 parts by weight of a mixture of 80.0 wt. As a comparative example, J Engineering S Super Early Strength SE (Note) film elongation of 0 shows almost the same elongation as Amu Mina cement/no gypsum additive. Other positive indications are the same as in Example 1.
Claims (1)
有し、アルミナセメントとセラコラとの割合がアルミナ
セメント1重量部に対してセラコラ約0.5〜7重量部
であシ、アルミナセメントとセラコラの和が高分子水分
散体100重量部に対し約10〜200重量部である塗
膜形成組成物。It contains alumina cement, Ceracola and a polymer water dispersion, the ratio of alumina cement and Ceracola is about 0.5 to 7 parts by weight per 1 part by weight of alumina cement, and the sum of alumina cement and Ceracola is The coating film-forming composition is about 10 to 200 parts by weight based on 100 parts by weight of the aqueous polymer dispersion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1659084A JPS60158269A (en) | 1984-01-30 | 1984-01-30 | Film-forming composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1659084A JPS60158269A (en) | 1984-01-30 | 1984-01-30 | Film-forming composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60158269A true JPS60158269A (en) | 1985-08-19 |
Family
ID=11920490
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1659084A Pending JPS60158269A (en) | 1984-01-30 | 1984-01-30 | Film-forming composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60158269A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5073197A (en) * | 1988-08-12 | 1991-12-17 | National Research Development Corporation | Cement compositions |
WO2001028956A1 (en) | 1999-10-19 | 2001-04-26 | Fosroc International Limited | Cementitious compositions and a method of their use |
WO2001028955A1 (en) * | 1999-10-19 | 2001-04-26 | Fosroc International Limited | Cementitious compositions and a method of their use |
US6926769B2 (en) * | 2001-04-12 | 2005-08-09 | Fosroc Mining International Limited | Cementitous compositions and a method of their use |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4847919A (en) * | 1971-10-22 | 1973-07-07 | ||
JPS53128624A (en) * | 1977-04-16 | 1978-11-09 | Idemitsu Kosan Co | Gypsum compound |
-
1984
- 1984-01-30 JP JP1659084A patent/JPS60158269A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4847919A (en) * | 1971-10-22 | 1973-07-07 | ||
JPS53128624A (en) * | 1977-04-16 | 1978-11-09 | Idemitsu Kosan Co | Gypsum compound |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5073197A (en) * | 1988-08-12 | 1991-12-17 | National Research Development Corporation | Cement compositions |
WO2001028956A1 (en) | 1999-10-19 | 2001-04-26 | Fosroc International Limited | Cementitious compositions and a method of their use |
WO2001028955A1 (en) * | 1999-10-19 | 2001-04-26 | Fosroc International Limited | Cementitious compositions and a method of their use |
US6869987B2 (en) | 1999-10-19 | 2005-03-22 | Minova International Limited | Cementitious compositions and a method of their use |
US6926769B2 (en) * | 2001-04-12 | 2005-08-09 | Fosroc Mining International Limited | Cementitous compositions and a method of their use |
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