JPH0343465A - Coating compound for interior of building structure - Google Patents
Coating compound for interior of building structureInfo
- Publication number
- JPH0343465A JPH0343465A JP17184589A JP17184589A JPH0343465A JP H0343465 A JPH0343465 A JP H0343465A JP 17184589 A JP17184589 A JP 17184589A JP 17184589 A JP17184589 A JP 17184589A JP H0343465 A JPH0343465 A JP H0343465A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- paint
- adsorbent
- interior
- coating compound
- 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
- 239000011248 coating agent Substances 0.000 title abstract 5
- 238000000576 coating method Methods 0.000 title abstract 5
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000011347 resin Substances 0.000 claims abstract description 23
- 229920005989 resin Polymers 0.000 claims abstract description 23
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 16
- 239000003463 adsorbent Substances 0.000 claims abstract description 13
- 239000000839 emulsion Substances 0.000 claims abstract description 11
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 8
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 7
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000003973 paint Substances 0.000 claims description 28
- 239000002131 composite material Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 229960005070 ascorbic acid Drugs 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 6
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 claims description 6
- 239000003513 alkali Substances 0.000 abstract 2
- 229940072107 ascorbate Drugs 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 25
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 239000002518 antifoaming agent Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000005192 partition Methods 0.000 description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 239000004567 concrete Substances 0.000 description 5
- 239000004570 mortar (masonry) Substances 0.000 description 5
- 235000004431 Linum usitatissimum Nutrition 0.000 description 4
- 240000006240 Linum usitatissimum Species 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 235000004426 flaxseed Nutrition 0.000 description 4
- 235000021388 linseed oil Nutrition 0.000 description 4
- 239000000944 linseed oil Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000004378 air conditioning Methods 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 229940046892 lead acetate Drugs 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 1
- FEYNFHSRETUBEM-UHFFFAOYSA-N N-[3-(1,1-difluoroethyl)phenyl]-1-(4-methoxyphenyl)-3-methyl-5-oxo-4H-pyrazole-4-carboxamide Chemical compound COc1ccc(cc1)N1N=C(C)C(C(=O)Nc2cccc(c2)C(C)(F)F)C1=O FEYNFHSRETUBEM-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- LZMJNVRJMFMYQS-UHFFFAOYSA-N poseltinib Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC1=NC(OC=2C=C(NC(=O)C=C)C=CC=2)=C(OC=C2)C2=N1 LZMJNVRJMFMYQS-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、美術館、博物館、資料館(以下「美術館等J
という。)等の壁面に塗装されて、アルカリ性ガスの発
生を防ぐ建築物内装用塗料に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention is applicable to art museums, museums, and archives (hereinafter referred to as "museums etc.").
That's what it means. ), etc., to prevent the generation of alkaline gas.
従来より、新築の美術館等のコンクリートやモルタル等
の壁面より発生するアルカリ性ガスは、貴重な美術品、
文献、資料等に色の変色を始めとする悪影響をおよぼす
ことがわかっている。そこで新築の美術館等では、竣工
直後に美術品などを展示せず、空調設備の運転を半年間
以上行い、展示環境を整えてから展示する、というはな
はだ不経済な準備を強いられている。Traditionally, alkaline gases generated from the walls of concrete and mortar in newly built art museums, etc., have been harmful to valuable works of art,
It is known to have negative effects on literature, materials, etc., including discoloration. For this reason, newly built museums and other museums are forced to make extremely uneconomical preparations, such as not displaying works of art immediately after construction is completed, and instead operating air conditioning equipment for more than half a year to prepare the exhibition environment before displaying them.
美術館等に於いては、コンクリートやモルタル等の壁面
の他、その展示機能上多くの間仕切壁が存在するが、こ
うした壁面1間仕切壁に塗装される塗料からもアマニ油
含浸紙を黄変させるアルカリ性のガスが発生しているこ
とが知見されており、これが美術品等への悪影響の1つ
とされている。In museums, etc., there are many partition walls in addition to walls made of concrete and mortar for their exhibition function, but the paint applied to these partition walls also contains alkaline substances that yellow the paper impregnated with linseed oil. It is known that gas is generated, and this is considered to be one of the negative effects on works of art.
したがって、美術館等を開設する場合には、空調設備を
半年間以上運転して、コンクリート、モルタル等の壁面
のみならず間仕切壁に塗装された塗膜からのアルカリ性
ガスの影響も排除しなくてはならない。そこで、コンク
リート、モルタル等の壁面や間仕切壁に塗装出来、アル
カリ性ガスの発生もなく、しかも内装材等から発生する
アルカリ性物質を除去できる建築物内装用塗料が強く望
まれている、というのが現状である。Therefore, when opening a museum, etc., air conditioning equipment must be operated for at least half a year to eliminate the effects of alkaline gas not only from walls such as concrete and mortar, but also from the paint film on partition walls. It won't happen. Therefore, there is a strong demand for paints for building interiors that can be applied to concrete, mortar, and other walls and partition walls, do not generate alkaline gases, and can remove alkaline substances generated from interior materials. It is.
かかる事態に鑑み、本発明者等は鋭意研究の結果、美術
館等の壁面に塗装可能な内装用塗料の開発に至ったもの
である。しかして本発明の要旨は、1、pH3〜8のエ
マルジョン樹脂または水溶性樹脂を主成分とする塗料に
アルカリ性ガスの吸着能を有する吸着剤を含むことを特
徴とする。建築物内装用塗料。In view of this situation, the inventors of the present invention have conducted extensive research and have developed an interior paint that can be painted on the walls of museums and the like. Therefore, the gist of the present invention is characterized in that an adsorbent having an ability to adsorb alkaline gas is contained in a paint mainly composed of an emulsion resin or a water-soluble resin having a pH of 3 to 8. Paint for building interiors.
2、吸着剤がFe (II)アスコルビン酸系複合剤で
ある。請求項1に記載の建築物内装用塗料。2. The adsorbent is a Fe (II) ascorbic acid complex. The building interior paint according to claim 1.
3、吸着剤がトリポリリン酸二水素アルミニウム系複合
剤である、請求項1に記載の建築物内装用塗料。3. The building interior paint according to claim 1, wherein the adsorbent is an aluminum dihydrogen tripolyphosphate composite agent.
に存する。exists in
塗料要素を大別すると、樹脂、顔料、溶剤、添加剤に分
類できる。これらをさらに個別に、アマニ油含浸紙の黄
色指数測定試験を行い、アルカリ性ガスの発生する要素
を取り除いていくという消去法により、塗料よりアルカ
リ性ガスが発生する要因を取り除いていった。Broadly speaking, paint elements can be classified into resins, pigments, solvents, and additives. We then conducted a yellow index test on paper impregnated with linseed oil, and used an elimination method to remove the elements that generate alkaline gas from the paint.
アマニ油含浸紙による黄色指数測定試験とは。What is the yellow index measurement test using linseed oil impregnated paper?
測定しようとするサンプルを密閉出来る瓶などの容器に
入れ、予め黄色指数を調整しておいたアマニ油含浸紙を
ふたの上部からつるし、密閉状態で20℃の恒温室内に
10日間放置後、アマニ油含浸紙の黄色指数を測定し、
初期の値からの増加値を評価する方法である0本法は、
東京国立文化財研究所で採用された試験法であり、詳細
は「建築知識 1984年 6月」に記載されている。Place the sample to be measured in an airtight container such as a bottle, hang linseed oil-impregnated paper whose yellow index has been adjusted in advance from the top of the lid, and leave it in a thermostatic chamber at 20°C for 10 days in a sealed state. Measure the yellow index of oil-impregnated paper,
The zero method, which is a method of evaluating the increase in value from the initial value, is
This is a test method adopted by the National Research Institute for Cultural Properties in Tokyo, and the details are described in ``Architectural Knowledge June 1984''.
本測定の結果、増加値が5未満であるサンプルは、アル
カリ性ガスの発生が無いか、あるいはごく僅少であると
評価した。As a result of this measurement, samples with an increase value of less than 5 were evaluated as having no alkaline gas generation or a very small amount of alkaline gas generation.
この結果、樹脂では酢酸ビニル系樹脂、顔料ではケイソ
ウ土系顔料、炭酸カルシウム系顔料、タルク系顔料、酸
化チタン系顔料、溶剤では高沸点系溶剤、添加剤では消
泡剤が、黄色指数の増加値がtJ’さく、一方、アクリ
ル系樹脂、安定化剤、防腐剤、界面活性剤等は黄色指数
の増加が大きいことが判明した。As a result, vinyl acetate resins are used as resins, diatomaceous earth pigments, calcium carbonate pigments, talc pigments, and titanium oxide pigments are used as pigments, high boiling point solvents are used as solvents, and antifoaming agents are used as additives, but the yellow index increases. On the other hand, it was found that acrylic resins, stabilizers, preservatives, surfactants, etc. had a large increase in yellow index.
さらに、pH3〜8のエマルジョン樹脂、または水溶性
樹脂であれば、Fa、(II)アスコルビン酸系複合剤
、トリポリリン酸二水素アルミニウム系複合剤といった
、アルカリ性ガスを吸着する吸着剤を適量添加すること
により、酢酸ビニル系樹脂だけではなく、アクリル系樹
脂などの樹脂に対しても黄色指数の増加値を5未満に抑
え得ることが判明した。pH3未満であると例えばF、
e(II)アスコルビン酸系複合剤はFe(■)とアス
コルビン酸が各々分子状に存在するにすぎず、錯イオン
を形成してアルカリ性ガスを吸着する反応を起こすこと
ができない、トリポリリン酸二水素アルミニウム系の吸
着剤を使用する場合にも同様の傾向がある。また、pH
8を超えるとアルカリ性ガスの吸着反応が十分に進行し
ないので好ましくない。Furthermore, if it is an emulsion resin with a pH of 3 to 8 or a water-soluble resin, an appropriate amount of an adsorbent that adsorbs alkaline gas, such as Fa, (II) ascorbic acid-based composite agent, or dihydrogen aluminum tripolyphosphate-based composite agent, may be added. As a result, it was found that the increase in yellow index can be suppressed to less than 5 not only for vinyl acetate resins but also for resins such as acrylic resins. If the pH is less than 3, for example, F,
e(II) Ascorbic acid-based composite agent is dihydrogen tripolyphosphate, in which Fe (■) and ascorbic acid each exist only in molecular form, and cannot cause a reaction to form complex ions and adsorb alkaline gases. A similar tendency exists when aluminum-based adsorbents are used. Also, pH
If it exceeds 8, the alkaline gas adsorption reaction will not proceed sufficiently, which is not preferable.
そこで、以上の知見に基づいてPH3〜8のエマルジョ
ン樹脂、または水溶性樹脂に好ましくはアルカリ性ガス
の発生要因の少ない顔料、添加剤を配合し、さらにアル
カリ性ガスの吸着能を有する吸着剤を適量添加すること
により、アルカリ性ガスの発生を防ぐ内装用塗料を開発
するに至ったものである。Therefore, based on the above findings, pigments and additives that are less likely to cause alkaline gas generation are preferably blended into an emulsion resin with a pH of 3 to 8 or a water-soluble resin, and an appropriate amount of an adsorbent that has alkaline gas adsorption ability is added. This led to the development of an interior paint that prevents the generation of alkaline gas.
塗料を構成する要素より、まずアルカリ性ガスの発生要
因を取り除き、さらにアルカリ性ガスの吸着能を持つ吸
着剤を添加することにより、使用できる樹脂の選択肢が
増えた。このことは、アマニ油含浸紙試験による結果で
は、酢酸ビニル系樹脂のみしか使用出来なかったことに
なるため、塗料配合を考える上で重要である。By first removing the causes of alkaline gas generation from the elements that make up the paint, and then adding an adsorbent that has the ability to adsorb alkaline gases, the range of resins that can be used has increased. This is important when considering paint formulation, since the results of the linseed oil-impregnated paper test indicate that only vinyl acetate resin could be used.
すなわち1本発明になる内装用塗料は、アルカリ性ガス
の発生要因を極力抑止しであるため、塗装して成膜後も
塗膜自体からアルカリ性ガスが発生することはなく、し
かも吸着剤の吸着能により、空気中に発生するアンモニ
ア等のアルカリ性物質を吸着するため美術館等の展示環
境の維持に極めてイj効であり、アルカリ性ガスの発生
を防ぎ、美術品等への悪影響を排除することができる。In other words, the interior paint according to the present invention suppresses the causes of alkaline gas generation as much as possible, so that alkaline gas is not generated from the paint film itself even after it is applied and the film is formed, and the adsorption capacity of the adsorbent is Because it adsorbs alkaline substances such as ammonia generated in the air, it is extremely effective in maintaining the exhibition environment of museums, etc., and can prevent the generation of alkaline gas and eliminate any negative effects on works of art. .
以下に実施例を挙げ本発明のより詳細な理解に供する。 Examples are given below to provide a more detailed understanding of the present invention.
当然のことながら本発明は以下の実施例のみに限定され
るものではない。Naturally, the present invention is not limited to the following examples.
実施例1
酢酸ビニルエマルジョン樹脂40部、炭酸カルシウム3
0部、酸化チタン20部、消泡剤1部、トリポリリン酸
二水素アルミニウム系複合剤9部、酢酸鉛工部を高速攪
拌機にて分散し、p、H3の白色水性内装用塗料1を得
た。Example 1 40 parts of vinyl acetate emulsion resin, 3 parts of calcium carbonate
0 parts of titanium oxide, 20 parts of titanium oxide, 1 part of antifoaming agent, 9 parts of aluminum dihydrogen tripolyphosphate composite agent, and lead acetate were dispersed using a high-speed stirrer to obtain white water-based interior paint 1 with p and H3. .
実施例2
アクリルエマルジョン樹脂40部、炭酸カルシウム30
部、酸化チタン20部、消泡剤1部、Fe (II)ア
スコルビン酸系複合剤10部を高速攪拌機にて分散し、
pH8の白色水性内装用塗料2を得た。Example 2 40 parts of acrylic emulsion resin, 30 parts of calcium carbonate
1 part, 20 parts of titanium oxide, 1 part of antifoaming agent, and 10 parts of Fe (II) ascorbic acid composite agent were dispersed using a high-speed stirrer.
A white aqueous interior paint 2 having a pH of 8 was obtained.
比較例1
アクリルエマルジョン樹脂40部、硫酸バリウム40部
、酸化チタン20部、消泡剤1部を高速攪拌機にて分散
し、p H8の白色水性内装用塗料3を得た。Comparative Example 1 40 parts of acrylic emulsion resin, 40 parts of barium sulfate, 20 parts of titanium oxide, and 1 part of antifoaming agent were dispersed using a high-speed stirrer to obtain a white aqueous interior paint 3 having a pH of 8.
比較例2
アクリルエマルジョン樹脂40部、炭酸カルシウム30
部、酸化チタン20部、消泡剤1部、トリポリリン酸二
水素アルミニウム系複合剤9部、酢酸鉛4部を高速攪拌
機にて分散し、p H2の白色水性内装用塗料4を得た
。Comparative Example 2 40 parts of acrylic emulsion resin, 30 parts of calcium carbonate
20 parts of titanium oxide, 1 part of an antifoaming agent, 9 parts of an aluminum dihydrogen tripolyphosphate composite agent, and 4 parts of lead acetate were dispersed using a high-speed stirrer to obtain a white aqueous interior paint 4 having a pH of 2.
比較例3
アクリルエマルジョン樹脂40部、炭酸カルシウム30
部、酸化チタン20部、消泡剤工部、Fa (II)ア
スコルビン酸系複合剤10部、アンモニア2部を高速攪
拌機にて分散し、pH9の白色水性内装用塗料5を得た
。Comparative Example 3 40 parts of acrylic emulsion resin, 30 parts of calcium carbonate
20 parts of titanium oxide, 20 parts of antifoaming agent, 10 parts of Fa (II) ascorbic acid-based composite agent, and 2 parts of ammonia were dispersed using a high-speed stirrer to obtain a white aqueous interior paint 5 having a pH of 9.
試験方法
白色水性内装用塗料1〜5をサンプルとして、各20g
を各々ガラス製広口ビンにいれ、ビンの上部に約1−の
アマニ油含浸紙を糸でつるし、ふたをして密閉し、20
℃の恒温室に10日間放置した。アマニ油含浸紙は試験
開始前黄色指数初期値を25に調整しておいたものを使
用した。Test method: 20g each of white water-based interior paints 1 to 5 as samples.
Place each in a wide-mouthed glass bottle, hang a piece of linseed oil-impregnated paper with a thread from the top of the bottle, close the lid, and seal the bottle.
It was left in a constant temperature room at ℃ for 10 days. The paper impregnated with linseed oil had its initial yellow index value adjusted to 25 before the start of the test.
結果
各サンプルの10日後のアマニ油含浸紙の黄色指数を測
定したところ、
実施例127 初期値より+2
実施例228 初期値より+3
比較例↓ 78 初期値より+53
比較例265 初期値より+40
比較例368 初期値より+43
であった。Results When the yellowness index of the linseed oil-impregnated paper of each sample was measured after 10 days, the results were as follows: Example 127: +2 from the initial value Example 228: +3 from the initial value Comparative example↓ 78: +53 from the initial value Comparative example 265: +40 from the initial value Comparative example 368 It was +43 from the initial value.
本発明になる内装用塗料は、塗膜自体から美術品等にと
って有害なアルカリ性ガスを発生しないことは勿論、空
気中に存在するアンモニア等のアルカリ性物質をも吸着
するので、コンクリート、モルタル等より発生するアル
カリ性ガスをマスキングし1間仕切壁から発生していた
アルカリ性ガスを吸着する効果がある。The interior paint of the present invention not only does not generate alkaline gas harmful to works of art from the paint film itself, but also adsorbs alkaline substances such as ammonia present in the air, so it does not emit alkaline gases from concrete, mortar, etc. It has the effect of masking the alkaline gas generated from the partition wall and adsorbing the alkaline gas generated from the partition wall.
したがって、美術館等において貴重な美術品を展示する
ためには絶対必要な、アルカリ性ガスが存在しない、す
なわち美術品等の変色の心配のない、展示に最適な環境
を提供することができる。Therefore, it is possible to provide an optimal environment for displaying works of art without the presence of alkaline gas, which is absolutely necessary for displaying valuable works of art in museums, etc., and without fear of discoloration of works of art.
しかも本発明による内装用塗料を塗装することにより、
従来の様な、開館前の半年間以上にもわたる空調設備の
運転による展示環境の整備は不要となるので、美術館等
の建設コスト低減、開館迄の工期短縮にも寄与すること
ができる。Moreover, by applying the interior paint according to the present invention,
Since it is no longer necessary to prepare the exhibition environment by operating air conditioning equipment for more than half a year before the museum opens, as in the past, it can contribute to reducing the construction costs of museums, etc. and shortening the construction period until the museum opens.
Claims (1)
主成分とする塗料にアルカリ性ガスの吸着能を有する吸
着剤を含むことを特徴とする、建築物内装用塗料。 2、吸着剤がFe(II)アスコルビン酸系複合剤である
、請求項1に記載の建築物内装用塗料。 3、吸着剤がトリポリリン酸二水素アルミニウム系複合
剤である、請求項1に記載の建築物内装用塗料。[Scope of Claims] 1. A paint for the interior of a building, characterized in that the paint is mainly composed of an emulsion resin or a water-soluble resin having a pH of 3 to 8 and contains an adsorbent capable of adsorbing alkaline gas. 2. The building interior paint according to claim 1, wherein the adsorbent is a Fe(II) ascorbic acid composite. 3. The building interior paint according to claim 1, wherein the adsorbent is an aluminum dihydrogen tripolyphosphate composite agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17184589A JPH0343465A (en) | 1989-07-11 | 1989-07-11 | Coating compound for interior of building structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17184589A JPH0343465A (en) | 1989-07-11 | 1989-07-11 | Coating compound for interior of building structure |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0343465A true JPH0343465A (en) | 1991-02-25 |
Family
ID=15930836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17184589A Pending JPH0343465A (en) | 1989-07-11 | 1989-07-11 | Coating compound for interior of building structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0343465A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10259325A (en) * | 1997-03-19 | 1998-09-29 | Sk Kaken Co Ltd | Water-based coating composition |
JP2002242331A (en) * | 2001-02-16 | 2002-08-28 | Takenaka Komuten Co Ltd | Method for blocking noxious gas generated from concrete |
JP2005194377A (en) * | 2004-01-07 | 2005-07-21 | Nippon Paint Co Ltd | Wall modification method |
JP2010101020A (en) * | 2008-10-21 | 2010-05-06 | Takenaka Komuten Co Ltd | Concrete structure reducing amount of emitted alkaline gas, and method for reducing amount of alkaline gas emitted from the concrete structure |
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---|---|---|---|---|
JPS60210675A (en) * | 1984-04-05 | 1985-10-23 | Kikusui Kagaku Kogyo Kk | Production of water paint having a deodorizing effect |
JPS61181467A (en) * | 1985-02-08 | 1986-08-14 | 王子製紙株式会社 | Deodorant |
JPS6335637A (en) * | 1986-07-30 | 1988-02-16 | Hokuetsu Seishi Kk | Water-based composition for coating or impregnation and worked product thereof |
JPS63219700A (en) * | 1987-03-04 | 1988-09-13 | 北越製紙株式会社 | Coating or impregnating aqueous composition and processed article |
JPS63281657A (en) * | 1987-05-13 | 1988-11-18 | Hidehiro Seishiyou | Deodorant base on iron and l-ascorbic acid and preparation thereof |
JPH02115281A (en) * | 1988-10-24 | 1990-04-27 | Hitachi Plant Eng & Constr Co Ltd | Process for coating interior material with coating material |
JPH02163173A (en) * | 1988-12-16 | 1990-06-22 | Kanpe Katei Toryo Kk | Aqueous deodorant coating |
JPH02180972A (en) * | 1988-12-29 | 1990-07-13 | Kanpe Katei Toryo Kk | Water-based deodorizing coating material |
-
1989
- 1989-07-11 JP JP17184589A patent/JPH0343465A/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60210675A (en) * | 1984-04-05 | 1985-10-23 | Kikusui Kagaku Kogyo Kk | Production of water paint having a deodorizing effect |
JPS61181467A (en) * | 1985-02-08 | 1986-08-14 | 王子製紙株式会社 | Deodorant |
JPS6335637A (en) * | 1986-07-30 | 1988-02-16 | Hokuetsu Seishi Kk | Water-based composition for coating or impregnation and worked product thereof |
JPS63219700A (en) * | 1987-03-04 | 1988-09-13 | 北越製紙株式会社 | Coating or impregnating aqueous composition and processed article |
JPS63281657A (en) * | 1987-05-13 | 1988-11-18 | Hidehiro Seishiyou | Deodorant base on iron and l-ascorbic acid and preparation thereof |
JPH02115281A (en) * | 1988-10-24 | 1990-04-27 | Hitachi Plant Eng & Constr Co Ltd | Process for coating interior material with coating material |
JPH02163173A (en) * | 1988-12-16 | 1990-06-22 | Kanpe Katei Toryo Kk | Aqueous deodorant coating |
JPH02180972A (en) * | 1988-12-29 | 1990-07-13 | Kanpe Katei Toryo Kk | Water-based deodorizing coating material |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10259325A (en) * | 1997-03-19 | 1998-09-29 | Sk Kaken Co Ltd | Water-based coating composition |
JP2002242331A (en) * | 2001-02-16 | 2002-08-28 | Takenaka Komuten Co Ltd | Method for blocking noxious gas generated from concrete |
JP4711276B2 (en) * | 2001-02-16 | 2011-06-29 | 株式会社竹中工務店 | How to shut off harmful gases from concrete |
JP2005194377A (en) * | 2004-01-07 | 2005-07-21 | Nippon Paint Co Ltd | Wall modification method |
JP4519469B2 (en) * | 2004-01-07 | 2010-08-04 | 日本ペイント株式会社 | Wall remodeling method |
JP2010101020A (en) * | 2008-10-21 | 2010-05-06 | Takenaka Komuten Co Ltd | Concrete structure reducing amount of emitted alkaline gas, and method for reducing amount of alkaline gas emitted from the concrete structure |
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