JPS61107979A - Method for preventing color staining due to exudation - Google Patents

Method for preventing color staining due to exudation

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Publication number
JPS61107979A
JPS61107979A JP17818785A JP17818785A JPS61107979A JP S61107979 A JPS61107979 A JP S61107979A JP 17818785 A JP17818785 A JP 17818785A JP 17818785 A JP17818785 A JP 17818785A JP S61107979 A JPS61107979 A JP S61107979A
Authority
JP
Japan
Prior art keywords
building materials
coated
silica sol
building material
basic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP17818785A
Other languages
Japanese (ja)
Other versions
JPH026581B2 (en
Inventor
Akitoshi Yoshida
明利 吉田
Masamichi Kohitsu
小櫃 正道
Takahiro Hori
孝廣 堀
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP17818785A priority Critical patent/JPS61107979A/en
Publication of JPS61107979A publication Critical patent/JPS61107979A/en
Publication of JPH026581B2 publication Critical patent/JPH026581B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To prevent the generation of color staining, by coating the surface of a building material with a stable silica gel coated with oxide of Zn, Mg, Pb, Zr or Sn before drying. CONSTITUTION:An org. acid salt or basic org. acid salt of Zn, Mg, Pb, Ti, Zr or Sn is mixed with a silica sol, wherein colloidal silica with a particle size of 2-150mum is dispersed in water or a hydrophylic org. solvent, to be reacted with said salt. By this method, a silica sol, wherein the surface of silica is coated with one of said metals, is obtained and applied to the surface of a base material such as a building material containing an exudative color substance such as lignin or tannin.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、滲出性着色物質を含有する建材の表面改質方
法、特に、特定の金属酸化物で表面被覆された安定なり
リカゾル全上記建材の表面に塗布し乾燥することによっ
て、内部に含まれる滲出性着色物質が表面に滲出するこ
とによる建材表面の着色汚損の生起を防ぐ方法に関する
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method for surface modification of building materials containing exudable coloring substances, and in particular to a method for surface modification of building materials containing exudable coloring substances, and in particular to methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing leachable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing leachable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances, and in particular, methods for surface modification of building materials containing exudable coloring substances. The present invention relates to a method for preventing colored stains on the surface of building materials due to leaching of exudable coloring substances contained therein to the surface by coating and drying.

従来の技術 滲出性着色物質を含有する建材は多く実用されている。Conventional technology Many building materials containing exudable coloring substances are in practical use.

例えば1通常の木材、木材合板、パーティクルボード、
上記の如き材料とスレート板0石膏板等を張り合せた積
ノー板、木粉、有機質ffl維等ti人させたセメント
或いは石膏板等はよく知られている例である。
For example, 1 normal wood, wood plywood, particle board,
Well-known examples include laminated wood boards made by laminating the above-mentioned materials with slate boards, gypsum boards, etc., and cement or gypsum boards made of wood flour, organic fibers, etc.

これら建材は、長期にわたる使用中に建材中に含まれる
着色物質が建材表面に滲出することによって、欠第に建
材表面が変色し、所謂着色汚損がしばしば生起する。こ
の着色汚損が、特に、室内の天井、a等美粧化表面上に
生起するがしばしばであった。この着色汚損を解消する
方法としては、洗液?用いて汚損表面を浄化する方法も
あるが、簡易には実施し難く、また。
During long-term use of these building materials, the coloring substances contained in the building materials ooze out onto the surface of the building material, causing the surface of the building material to discolor over time, often resulting in so-called colored staining. This colored stain often occurred, especially on decorative surfaces such as indoor ceilings and a. Is there a way to remove this colored stain with washing liquid? Although there is a method of cleaning contaminated surfaces by using

完全に原状にまで浄化し難い。It is difficult to completely purify it to its original state.

この着色汚損を解消する別の方法としては。Another way to get rid of this coloring stain is.

汚損表面に塗料を用いて再塗装隠ぺいする方法も知られ
ているが、新たに形成された金膜は。
It is also known to cover up contaminated surfaces by repainting them with paint, but it is difficult to hide the newly formed gold film.

着色物質の滲出防止能力を有しないために、長期にわた
る使用中には再びその表面vcT’層から着色物質が滲
出し1着色汚損が繰り返されるという欠点を有する。
Since it does not have the ability to prevent coloring substances from oozing out, it has the disadvantage that coloring substances ooze out from the surface vcT' layer again during long-term use, resulting in repeated color staining.

発明が解決しようとする問題点 本発明の目的は0着色物質の滲出防止能力と併せて建材
との接着性、耐水性、耐候性、耐久性等にも優れるa膜
を建材表面に形成させることによって9着色物質の滲出
による建材表面の着色汚損を防ぐ方法を提供することに
ある。
Problems to be Solved by the Invention The purpose of the present invention is to form an a-film on the surface of building materials that has excellent adhesion to building materials, water resistance, weather resistance, durability, etc. as well as the ability to prevent coloring substances from oozing out. According to the present invention, it is an object of the present invention to provide a method for preventing colored stains on the surface of building materials due to leaching of colored substances.

問題点を解決するための手段 本発明の着色物質の滲出による建材表面の着色汚損の防
止方法は、亜鉛、マグネシウム、鉛。
Means for Solving the Problems The method of the present invention for preventing colored stains on the surface of building materials due to leaching of colored substances includes zinc, magnesium, and lead.

チタン、ジルコニウム又は錫の酸化物で被覆された安定
fx717カゾルt−建材の表面に塗布した後乾燥する
ことを特徴とする。
Stable fx717 Kasol T- coated with titanium, zirconium or tin oxides is characterized in that it is applied to the surface of the building material and then dried.

本発明の方法が適用される建材としては、無機系、有機
系、及び無機、有機複合系のものであって、内部から着
色物質が建材表面に滲出することにより、建材表面の着
色汚損が生起するものである。その例としては、木材を
原料にして得られる板、柱0合板1紙、パーティクルボ
ード;無機セメント2石−Wf4に木材扮末、木材粒、
有機質繊維1紙の砕片、有機質樹脂粉末等を混入させ成
形硬化させることにより得られる建材;有機質の紙、木
質の板、含酸樹脂シート等と無機質のスレート板、セメ
ント、石膏等の硬化板を接着剤を用いて積層張り合せて
得られる積層板;コンクリート、モルタル、石膏、スレ
ート等の基材の表面に着色物質を含む塗Mを形成させて
得られる化粧建材;前記着色物質の滲出により既に着色
汚損された各種の建材;その他、既に嬬築物の一部とし
て使用中のもの。
The building materials to which the method of the present invention is applied include inorganic, organic, and inorganic/organic composite materials, and coloring and staining of the surface of the building material occurs due to colored substances exuding from inside onto the surface of the building material. It is something to do. Examples include boards made from wood, 0 pillars, 1 plywood, 1 paper, particle board; 2 stones of inorganic cement - Wf4 with wood powder, wood particles,
A building material obtained by mixing organic fibers with paper fragments, organic resin powder, etc. and molding and hardening; combining organic paper, wood boards, acid-containing resin sheets, etc. with inorganic hardened boards such as slate boards, cement, and plaster. A laminate obtained by laminating and bonding together using an adhesive; A decorative building material obtained by forming a coating M containing a colored substance on the surface of a base material such as concrete, mortar, plaster, or slate; Various colored and soiled building materials; and other materials already in use as part of the building.

例えば、タバコの煙が耐着することにより表面が着色汚
損されている壁面、天井等が挙げられる。
Examples include walls, ceilings, etc. whose surfaces are colored and stained due to the adhesion of cigarette smoke.

これら建材中に含まれる滲出性着色物質の例としては、
リグニ/、タンニン、ニコチ/フミン酸、酸性及び塩基
性の色素1例えば、コンゴーレッド、ボルドレッド、ニ
オクン、ピクリン酸、メチレンブルー、マラカイトグリ
ーン、クリンイジン等が挙げられる。
Examples of exudable coloring substances contained in these building materials include:
Ligni/tannin, nicotine/humic acid, acidic and basic pigments 1 Examples include Congo red, bold red, niocone, picric acid, methylene blue, malachite green, clinidine, and the like.

本発明に用いられる亜鉛、マグネシウム、鉛。Zinc, magnesium, and lead used in the present invention.

チタン、ジルコニウム、又は錫の酸化物で被覆され念安
定なシリカゾルは、水、R水性有機溶媒又はこれらの混
合液中に粒径2〜150Fllμのコロイド状シリカが
分散するシリカゾルと亜鉛。
The ultrastable silica sol coated with titanium, zirconium, or tin oxide is a silica sol in which colloidal silica with a particle size of 2 to 150 Flμ is dispersed in water, an R aqueous organic solvent, or a mixture thereof, and zinc.

マグネシウム、鉛、チタン、ジルコニウム又は場の有機
lR塩、塩基性有機酸塩、無機酸塩若しくは塩基性無機
酸塩が水、親水性有機溶媒又はこれらの混合液に溶解し
た溶液と全混合灰石させることにより得られ、或いは特
開昭47−42600号公報、米国特許第289279
7号明則書等の記載に基いて容易に製造される。
Totally mixed ash with a solution of magnesium, lead, titanium, zirconium or in situ organic IR salt, basic organic acid salt, inorganic acid salt or basic inorganic acid salt dissolved in water, a hydrophilic organic solvent or a mixture thereof. or JP-A-47-42600, U.S. Patent No. 289279.
It is easily manufactured based on the description in No. 7 Meiji Rules and the like.

上記シリカゾルの分散媒として用いられる有機溶媒は、
上記金属の塩の溶媒として用いられる有機溶媒とは異な
ってもよいが、同じであることが好ましい。これら有機
溶媒としては1例えば、メタノール、エタノール、イン
グロバノール、エチレングリコール、グリセリン等アル
コール類;アセトノ、メチルエチルケトン等ケト/類;
ソの他モルフォリン、ジメチルホルムアルデヒド等も挙
げられ、適宜選定して用いられる。上記7リカゾルは、
公知の方法9例えば。
The organic solvent used as a dispersion medium for the silica sol is
The organic solvent may be different from the organic solvent used as the solvent for the metal salt, but is preferably the same. Examples of these organic solvents include 1 alcohols such as methanol, ethanol, inglobanol, ethylene glycol, and glycerin; keto/types such as acetonate and methyl ethyl ketone;
In addition to this, morpholine, dimethyl formaldehyde, etc. may also be mentioned, and these may be appropriately selected and used. The above 7 ricazol is
Known methods 9 e.g.

水ガラス溶液を陽イオ/交換樹脂で処理することにより
得られる希薄活性珪酸溶液を熟成し必要KEじアルカリ
添加することにより得られ。
It is obtained by aging a dilute activated silicic acid solution obtained by treating a water glass solution with a cation/exchange resin and adding the necessary KE dialkali.

S10.濃度約1〜55Xであり、かつ、  SiO,
/M、0(MはLL ML L NH−又は有機塩基の
陽イオン基金示す、、)モル比が10以上であるものが
用いられる。上記亜鉛、マグネシウム、鉛、チタン。
S10. a concentration of about 1 to 55X, and SiO,
/M, 0 (M indicates LL ML L NH- or a cationic base of an organic base, ) having a molar ratio of 10 or more is used. Above zinc, magnesium, lead, titanium.

ジルコニウム及び錫の塩としては1例えば、これら金属
の塩酸塩、硝酸塩、りん酸塩、硫酸塩。
Examples of zirconium and tin salts include hydrochlorides, nitrates, phosphates, and sulfates of these metals.

硼酸塩、酢酸塩、蟻酸塩、修酸塩;塩基性塩酸塩2.塩
基性硝酸塩、塩基性りん酸塩、塩基性硫酸塩、塩基性硼
酸塩、塩基性酢酸塩、塩基性蟻酸塩、塩基性蟻酸塩;こ
れら塩、塩基性塩の複塩;Li、Ha、に等アルカリ金
属、アンモニア等の虚塩;含窒素有機塩基;例えば、メ
チルアミン。
Borate, acetate, formate, oxalate; basic hydrochloride2. Basic nitrate, basic phosphate, basic sulfate, basic borate, basic acetate, basic formate, basic formate; these salts, double salts of basic salts; Li, Ha, Empty salts of alkaline metals, ammonia, etc.; nitrogen-containing organic bases; for example, methylamine.

ジエチルアミン、トリメチルアミン、モノメチルトリエ
タノールアンモニウム水酸化物、グアニジ7等第1級ア
ミン、第2級アミン、第3級アミン、第4級ア/モニク
ム水酸化物等の酸塩が挙げられる。上記金、gZn、 
Mgt Pb、 Ti、 Zr又はSn倉qで、上記有
機酸及び無機酸の酸基をRで。
Examples include acid salts such as diethylamine, trimethylamine, monomethyltriethanolammonium hydroxide, primary amines such as guanidi7, secondary amines, tertiary amines, and quaternary a/monic hydroxides. The above gold, gZn,
Mgt Pb, Ti, Zr or Sn, the acid group of the above organic acid and inorganic acid is R.

また、上記LL Na、 K #のアルカリ金属、  
NH,及び含窒素有機塩基の1場イオン基fcTでそれ
ぞれ表わせば0本発明に用いられる亜鉛、マグネシウム
、鉛、チタン、ジルコニウム又は錫の酸化物で被覆され
た安定なシリカゾルを調製する丸めに用いられる上記金
属の有機酸塩、塩基性有機酸塩、無faI#!塩及び塩
基性無機酸塩の溶液中には、上記塩基の陽イオン基又は
酸基と金属とがそれぞれQ、/Rのモル比α1〜10又
はQ/Tのモル比α05〜30の割合で含まれているこ
とが好ましく、また、上記金属の塩、塩基性塩又は酸塩
は前記溶媒中に2〜50Xの濃度で含まれていることが
好ましい。
In addition, the above LL Na, K # alkali metal,
NH, and the one-field ionic group fcT of a nitrogen-containing organic base, respectively expressed as 0. Organic acid salts of the above metals, basic organic acid salts, no faI#! In the solution of the salt and the basic inorganic acid salt, the cationic group or acid group of the base and the metal are present at a molar ratio of Q and /R of α1 to 10 or a molar ratio of Q/T of α05 to 30, respectively. Preferably, the metal salt, basic salt, or acid salt is contained in the solvent at a concentration of 2 to 50X.

上記金属の酸化物で被覆されたコロイド状7リカ粒子は
、シリカゾルからのコロイド粒子表面の一部又は全部が
酸素原子を介して上記金属原子と化学結合しているか又
は上記金属が酸化物の型でコロイド粒子表面に吸着され
た状態で7リカのコロイド粒子表面を被覆している構造
のものである。
The colloidal particles coated with the oxide of the metal mentioned above are either partially or entirely chemically bonded to the metal atom via oxygen atoms on the surface of the colloid particle from the silica sol, or the metal is in the form of an oxide. It has a structure in which the surface of the colloid particles is coated with 7 liters of colloid particles while being adsorbed onto the surfaces of the colloid particles.

本発明に用いられる上記金属酸化物で被覆された安定な
りす力ゾル中には、上記金属の塩が若干溶存していても
差支えないが、その量は少ない方がよい。
In the stable sopping sol coated with the metal oxide used in the present invention, a small amount of the metal salt may be dissolved, but the smaller the amount, the better.

本発明に用いられる上記金属の酸化物で被゛覆された安
定な7リカゾル中には、  Sin、が2〜45X、上
記金属の酸化物は1101〜8X程度含まれているもの
が好ましい。
The stable 7-lykasol coated with the oxide of the above-mentioned metal used in the present invention preferably contains about 2 to 45X of Sin and about 1101 to 8X of the oxide of the above-mentioned metal.

上記金属酸化物で被覆された安定なりリカゾルt−建材
の表面に塗布する方法としては1通常のスプレー、刷毛
等を用いる方法でよい。また。
As a method for applying it to the surface of the stable Ricasol T-building material coated with the metal oxide, a conventional method using a spray, a brush, etc. may be used. Also.

乾燥も自然乾燥1強制乾燥のいずれでもよい。Drying may be either natural drying or forced drying.

作用 上記金属酸化物で被覆され九安定なりリカゾルを建材表
面に塗布するのみでは、aWR面層の礒綱孔、C上記ゾ
ルが含浸するか又は、建材表面に液状膜が形成されるの
みである。このゾル白木には着色物質の滲出を防止する
能力はないので、上記ゾルを不可逆的にゲル化させる必
要がある。このゲル化は、建材表面に塗布することによ
って形成され免液状膜を乾燥脱水することによって容易
に達成される。上記亜鉛、マグネ7ウム、チタ/、ジル
コニウム、鉛又ハ場の酸化物で被覆されたコロイド状ク
リ力は乾燥脱水の際建材表面と強く結合するので、上記
ゾルを建材表面に塗布した後乾燥することによって建材
表面に強固に接着した硬化塗膜が形成される。
Effect: If only the stable lycasol coated with the above metal oxide is applied to the surface of the building material, the pores of the aWR surface layer will be impregnated with the above sol, or a liquid film will only be formed on the surface of the building material. . Since this sol plain wood does not have the ability to prevent coloring substances from oozing out, it is necessary to irreversibly gel the sol. This gelation is easily achieved by drying and dehydrating the liquid-repellent membrane formed by applying it to the surface of the building material. The colloidal crystals coated with the oxides of zinc, magnesium, titanium, zirconium, lead, and haba bond strongly with the surface of building materials during drying and dehydration, so the sol is applied to the surface of the building materials and then dried. By doing so, a cured coating film that firmly adheres to the surface of the building material is formed.

本発明による着色物質の滲出による建材表面の着色汚損
の防止は、上記金属酸化物で表面積1されたコミイド状
シリカ粒子のゲル化した硬化層が着色物質を吸着捕捉す
る能力が極めて強いことによるものと考えられる。
The present invention prevents colored stains on the surface of building materials due to oozing of colored substances because the gelled hardened layer of comidoid silica particles whose surface area is made up of the metal oxide has an extremely strong ability to adsorb and capture colored substances. it is conceivable that.

実施例1 (イク 金属酸化物で被覆された安定なシリカゾルの調
製 510w儂220X 、sio、 /Ha、 o モt
b比5f](1゜コロイド粒子の径14鵬μの水性シリ
カゾル324p 、!−slo、 9度50 N 、 
810./Ha、 Oモtb比9′O。
Example 1 Preparation of stable silica sol coated with metal oxide 510w 220X, sio, /Ha, omot
b ratio 5f] (1° colloidal particle diameter 14μ aqueous silica sol 324p, !-slo, 9 degrees 50 N,
810. /Ha, Omotb ratio 9'O.

コロイド粒子の径12mμの水性シリカゾル120fを
攪拌下に混合し、更にこの液中へ酢酸亜鉛。
Aqueous silica sol 120f with a colloidal particle diameter of 12 mμ is mixed with stirring, and zinc acetate is added into this solution.

に、激しい攪拌下に徐々に77O、t 、添加終f後室
温において更に5時間強力攪拌し九後、103tD 7
 y モニア水z4Fと水1 (16ft−加えPH’
!i−4,7に調節することにより、第1表に記載され
た組成を有するゾル(Ll )、 (r、+、 )、 
D+1 )、 (Ll )及び(ム)をそれぞれy4製
した。
After the addition was completed, the mixture was gradually stirred vigorously at room temperature for 5 hours at 77O, t, with vigorous stirring, and after 103tD, 7
y Monia water z4F and water 1 (16ft-added PH'
! By adjusting i-4,7, the sol (Ll), (r, +, ), having the composition listed in Table 1,
D+1), (Ll) and (Mu) were each produced in y4.

(a)  塗膜試験 上記げ)において調製されたゾル(I4) t 、木材
合板(S、)の表面に12017−の割付で刷毛塗りし
、1夜自然乾燥した後、この表面に更にポ176”ff
iビニルエマルジ冒ン塗料(白色)をスプレー金層いて
2009/ぜの割会で吹付は上塗りし室温で1日間乾燥
することにより化粧合板(P、)を傅九。仄いてこの化
粧板(P、)を50℃で湿度100Xの空気中に7日間
静置した後風乾し表面を目視fIISしたが1表面の変
色は全く認められなかっな。別途上記化粧板(P、)の
表面36clIに5仁の水を滴載し、自然乾燥を待って
表面を目視観察し念が矢張り変色は全く認められなかつ
念。
(a) Coating film test The sol (I4) t prepared in above) was applied with a brush to the surface of wood plywood (S,) with a distribution of 12017-, and after air drying overnight, the surface was further coated with 176 "ff
I Sprayed a gold layer of vinyl emulsion paint (white) and applied a top coat in 2009/Ze, and dried it at room temperature for 1 day to make decorative plywood (P). This decorative board (P) was allowed to stand for 7 days at 50° C. and 100× humidity, then air-dried and the surface was visually inspected using fIIS, but no discoloration was observed on the surface. Separately, 5 drops of water was placed on 36 clI of the surface of the above decorative board (P), and after waiting for it to dry naturally, the surface was visually observed to ensure that no discoloration was observed.

実施例2 10年間使用され、タバコの煙で黄褐色に汚損された木
材合板の天井板(S、)をはずし取り。
Example 2 A wood plywood ceiling board (S,) that had been used for 10 years and was stained yellowish-brown by cigarette smoke was removed.

このものから実施例1 (&”)と同様にして化粧合板
(pt)’を得、更に実施例1 (”)と同様にして2
橿の方法で塗膜の試験を行なったところ、いずれの試験
においても塗膜表面の変色は全く認められなかった。
From this material, decorative plywood (pt)' was obtained in the same manner as in Example 1 (&''), and 2
When the coating film was tested using the method described by Kashi, no discoloration of the coating film surface was observed in any of the tests.

実施例3 実施例1(インで調製されたゾル(L、)〜(L、)と
Example 3 Example 1 (sols (L, ) to (L, ) prepared with in.

実施例1及び2に用いたものと同じ木材合板(S、)及
び(S、)とを用い、実施例1(ロ)と同様にして第2
表に示す化粧合板(P、)〜(pu)を得、更に塗膜試
験を行なったが、いずれも塗膜表面の変色は認められな
かった。
Using the same wood plywood (S, ) and (S,) as used in Examples 1 and 2, a second
Decorative plywoods (P, ) to (pu) shown in the table were obtained, and a coating test was further conducted, but no discoloration was observed on the coating surface in any case.

第  2  表 比較例1 実施例1(−に用いた分散液(Ll)の代わりに。Table 2 Comparative example 1 Instead of the dispersion (Ll) used in Example 1 (-).

810、30 X、  SiO,/Na、0モル比90
 、 =l oイド°粒子径121μのシリカゾルを用
い、実施例1(ロ)と同様にして化粧合板(C1)を得
、更にこのものを実施例1 (”)と同様にして2種の
方法で塗膜の試験を行なったところ、いずれの試験にお
いても塗膜表面の黄変を認めたう 更に実施例2に用いたものと同じ天井板(S、)から上
記同様にして化粧合板(as)を得、このものの塗膜試
験を行なったところ1両試験の結果。
810, 30X, SiO,/Na, 0 molar ratio 90
A decorative plywood (C1) was obtained in the same manner as in Example 1 (b) using a silica sol with a particle diameter of 121 μm, and this material was further processed in the same manner as in Example 1 ('') using two methods. When tests were conducted on the paint film, yellowing of the paint film surface was observed in all tests.Furthermore, decorative plywood (AS ) was obtained, and a coating test was conducted on this product, and the results were 1-car test.

いずれも塗膜表面は褐色を帯びた黄色に変色した。In both cases, the paint film surface turned brownish yellow.

実施例へ (イ)金属酸化物で被覆された安定なシリカゾルの調−
WSi2、20 N 、  810./Ha、Oモル比
9B、コaイド状シリカ粒子径14m−μ、 PFi&
 2の水性シリカゾルに、第3表記載の組成となるよう
に、ゾル(−)としては亜鉛酸カリウムの水溶液を、ゾ
ル(ム)としては鉛酸ナトリウムの水溶液を夫々強力攪
拌下に混合し、添加終了後更に1時間強力攪拌を続けた
後、これに更に硼酸水溶液を添加することにより、ゾル
(L、)及び (ム)を調製した。
To Examples (a) Preparation of stable silica sol coated with metal oxide
WSi2, 20 N, 810. /Ha, O molar ratio 9B, colloidal silica particle diameter 14 m-μ, PFi&
To the aqueous silica sol of No. 2, an aqueous solution of potassium zincate as the sol (-) and an aqueous solution of sodium leadate as the sol (mu) were mixed under strong stirring so that the composition was as shown in Table 3. After the addition was completed, strong stirring was continued for another hour, and then an aqueous boric acid solution was further added to prepare sols (L,) and (M).

(C2)  塗膜の試験 上記ゾル(L、)と(ム)及びりん鉱石中に含まれる有
機質着色物質を含む石膏プラスター成形板(S、)を用
いた以外は実施例1(ロ)と同様にして。
(C2) Test of coating film Same as Example 1 (B) except that the above-mentioned sols (L, ) and (M) and gypsum plaster molded board (S,) containing an organic coloring substance contained in phosphate rock were used. Do it.

(L、)からは(PH) @ (LP)からは(ptJ
の各化粧板をりくり、塗膜の試験を行なったところ、い
ずれも表面の変色は認められなかった。
From (L,) is (PH) @ (LP) is (ptJ
When each of the decorative boards was cut out and a coating test was conducted, no discoloration was observed on the surface of any of them.

実施例5 (イ) ジルコニアで被覆された安定なシリカゾルの調
製S、io、 15 X、  S10./Na、Oモル
比900.ニアGlイド粒子径71μの水−メタノール
(水:メタノールの重量比90:10の混せ液)シリカ
ゾル8002にZr0.5 X f:含む塩基性蟻酸ジ
ルコニウム水溶液全強力攪拌下に徐々に添加し、添加終
了後引き続き2時間強力攪拌することにより! S10*  ” X−ZrOs 1.5 X、蟻酸1.
\X、メタメタノール8含?含ルコニアで被覆された安
定なシリカゾル(L、)を調製した。
Example 5 (a) Preparation of stable silica sol coated with zirconia S, io, 15 X, S10. /Na,O molar ratio 900. A basic zirconium formate aqueous solution containing Zr0.5X f: was gradually added to silica sol 8002 (mixture of water and methanol at a weight ratio of 90:10) with a near Glioid particle size of 71μ under full stirring, By continuing to stir vigorously for 2 hours after the addition is complete! S10*”X-ZrOs 1.5X, formic acid 1.
\X, Contains 8 methanol? A stable silica sol (L,) coated with zirconia was prepared.

(ロ) 塗膜の試験 市販壁紙接着用の4種の接着剤100?それぞれに上記
ゾル(L、)i 20 f添加混練することにより、下
記第4表記載の複合接着剤(DI)、 (DI)、(D
、)及びCD、)で調製した。
(b) Paint film test: 4 types of commercially available adhesives for wallpaper adhesive 100? By adding and kneading the above-mentioned sol (L,) i 20 f, the composite adhesives (DI), (DI), (D
, ) and CD, ).

第  4  表 次いで、前記木材合板(SI)の表面に上記接着剤(D
I) 〜(DI ) を各70 fltdの割合で塗布
し。
Table 4 Next, the above adhesive (D) was applied to the surface of the wood plywood (SI).
I) to (DI) were applied at a rate of 70 fltd each.

直ちに市販の日本紙からなる壁紙を張りつけた後、7日
間25℃で相対湿度40〜60Xの空気中に静置するこ
とにより、@4表記載の壁紙張り付は板(罵)、 (I
ff) 、 (XI)及び(XI) t−得た。
Immediately paste wallpaper made of commercially available Japanese paper, and then leave it in air at 25°C and relative humidity of 40 to 60X for 7 days.
ff), (XI) and (XI) t- were obtained.

次にこの板(xl)〜(X、)を温度20〜55℃。Next, the plates (xl) to (X,) were heated to a temperature of 20 to 55°C.

相対湿度50〜100Xの浴場の壁面に固定し1ケ月放
置したが壁紙表面には変色、不特定変色模様の発生、剥
離、ふくれ等は全く認められなかった。
The wallpaper was fixed on the wall of a bathroom with a relative humidity of 50 to 100X and left for one month, but no discoloration, generation of unspecified discoloration patterns, peeling, blistering, etc. were observed on the wallpaper surface.

比較例2 Si0.12N、 810./Ha、Oモル比1000
.コロイド粒子径7橢μの水性シリカゾルを上記分散液
(III)の代りに用いた以外は実施例5と同様にして
壁紙を張りつけた板について試験を行なったところ、上
記シリカゾルとアクリル系樹脂接着剤との複合接着剤を
用いたものでは7日後に斑点状のじみが発生し、またポ
リ酢酸ビニル接着剤との複合接着剤を用いたものでは1
ケ月後に褐色の着色が発生−し、尿素樹脂接着剤との複
合接着剤及びポリ酢酸ビニル接着剤との複合接着剤を用
いたものは両者共不特定変色模様が発生した。
Comparative Example 2 Si0.12N, 810. /Ha, O molar ratio 1000
.. A test was conducted on a board pasted with wallpaper in the same manner as in Example 5, except that an aqueous silica sol with a colloidal particle size of 7 μm was used instead of the dispersion (III). When using a composite adhesive with polyvinyl acetate, spot-like bleeding occurred after 7 days, and when using a composite adhesive with polyvinyl acetate adhesive.
After several months, brown discoloration occurred, and in both the composite adhesive with urea resin adhesive and the composite adhesive with polyvinyl acetate adhesive, an unspecified discoloration pattern occurred.

発明の効果 上記の如く本発明によると、建材表面に極めて簡易に金
属酸化物で被覆されたシリカゾルの硬化被膜を形成させ
ることができ、また、この硬化被膜によって内部から滲
出する着色物質が捕捉されるために建材表面の着色汚損
が防止されろう ifc、本発明に用いられる金属酸化物で被覆されたシ
リカゾルは1種々の添加剤と混合することができるので
、塗料、塗材、ソーラー、パテ、接着剤等の彩りでも用
いることができる。
Effects of the Invention As described above, according to the present invention, a hardened film of silica sol coated with a metal oxide can be formed on the surface of a building material very easily, and colored substances exuding from the inside can be captured by this hardened film. The silica sol coated with metal oxide used in the present invention can be mixed with various additives, so it can be used in paints, coating materials, solar, putty, etc. It can also be used as a colored adhesive.

北記添・1口剤としては、・、分粒状のンリカ、ベノ°
トナイト、ケイソウ土、パライト、炭酸カル7ウム、天
然岩石類、砂類等骨材;界面活注剤、ポリビニルアルコ
ール、メチルセルa−ス、カルボキンメチルセルロース
、ポリアクリル酸等分散剤又は増粘剤;ポリ酢酸ビニル
エマルジぢン。
As a 1-mouth tablet with Kitaki additives,...
Aggregates such as tonite, diatomaceous earth, pallite, calcium carbonate, natural rocks, and sand; Dispersants or thickeners such as surfactant pouring agents, polyvinyl alcohol, methylcellulose, carboquine methylcellulose, and polyacrylic acid; Polyvinyl acetate emulsion.

ゴムラテックス、水溶性メラミン樹脂、エチレン−酢酸
ビニル共重合体エマルジ=I/、ポリウレタン、アルキ
ッド樹脂、エポキシ樹脂等の水性分散体、その他の有機
質パイ/ダー;その他層色顔料、消泡剤、防腐剤等が挙
げられる。
Rubber latex, water-soluble melamine resin, ethylene-vinyl acetate copolymer emulsion I/, aqueous dispersion of polyurethane, alkyd resin, epoxy resin, other organic pigments, other layer color pigments, antifoaming agents, preservatives agents, etc.

上記シリカゾルと添加剤を含有する塗料、接着剤、シー
ラー、パテ等も乾燥硬化後は、建材表面との接着性、耐
水性、耐候性に優れ、しかも9着色性物質の滲出による
表面汚損の生起しない建材が得られる。
After drying and curing, paints, adhesives, sealers, putty, etc. containing the above-mentioned silica sol and additives have excellent adhesion to building material surfaces, water resistance, and weather resistance, and they do not cause surface staining due to leaching of coloring substances. You can obtain building materials that do not require

Claims (1)

【特許請求の範囲】[Claims] 亜鉛、マグネシウム、鉛、チタン、ジルコニウム又は錫
の酸化物で被覆された安定なシリカゾルを建材の表面に
塗布した後乾燥することを特徴とする着色物質の滲出に
よる建材表面の着色汚損を防止する方法。
A method for preventing colored staining of the surface of building materials due to exudation of colored substances, characterized by applying a stable silica sol coated with oxides of zinc, magnesium, lead, titanium, zirconium, or tin to the surface of the building material and then drying it. .
JP17818785A 1985-08-13 1985-08-13 Method for preventing color staining due to exudation Granted JPS61107979A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17818785A JPS61107979A (en) 1985-08-13 1985-08-13 Method for preventing color staining due to exudation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17818785A JPS61107979A (en) 1985-08-13 1985-08-13 Method for preventing color staining due to exudation

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP12049877A Division JPS5454152A (en) 1977-10-08 1977-10-08 Prevention of staining with exuded color

Publications (2)

Publication Number Publication Date
JPS61107979A true JPS61107979A (en) 1986-05-26
JPH026581B2 JPH026581B2 (en) 1990-02-09

Family

ID=16044118

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17818785A Granted JPS61107979A (en) 1985-08-13 1985-08-13 Method for preventing color staining due to exudation

Country Status (1)

Country Link
JP (1) JPS61107979A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08225767A (en) * 1994-10-28 1996-09-03 Hoechst Ag Water-base dispersion for primer
EP0666292A3 (en) * 1994-02-07 1997-01-02 Dainichiseika Color Chem Coating composition and coating film composition.
JP2016535691A (en) * 2013-11-08 2016-11-17 ベーカー ギウリニ ゲゼルシャフト ミット ベシュレンクテル ハフツングBK Giulini GmbH Means and method for preventing tannin migration from wood

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0666292A3 (en) * 1994-02-07 1997-01-02 Dainichiseika Color Chem Coating composition and coating film composition.
JPH08225767A (en) * 1994-10-28 1996-09-03 Hoechst Ag Water-base dispersion for primer
JP2016535691A (en) * 2013-11-08 2016-11-17 ベーカー ギウリニ ゲゼルシャフト ミット ベシュレンクテル ハフツングBK Giulini GmbH Means and method for preventing tannin migration from wood

Also Published As

Publication number Publication date
JPH026581B2 (en) 1990-02-09

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