Nothing Special   »   [go: up one dir, main page]

JPH05295338A - Aqueous emulsion adhesive - Google Patents

Aqueous emulsion adhesive

Info

Publication number
JPH05295338A
JPH05295338A JP10300592A JP10300592A JPH05295338A JP H05295338 A JPH05295338 A JP H05295338A JP 10300592 A JP10300592 A JP 10300592A JP 10300592 A JP10300592 A JP 10300592A JP H05295338 A JPH05295338 A JP H05295338A
Authority
JP
Japan
Prior art keywords
aqueous emulsion
water
vinyl chloride
adhesive
cistern
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
Application number
JP10300592A
Other languages
Japanese (ja)
Inventor
Makoto Shimada
誠 島田
Masao Seno
正男 勢能
Eiji Makita
栄司 牧田
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.)
Kobayashi KK
Original Assignee
Kobayashi KK
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 Kobayashi KK filed Critical Kobayashi KK
Priority to JP10300592A priority Critical patent/JPH05295338A/en
Publication of JPH05295338A publication Critical patent/JPH05295338A/en
Pending legal-status Critical Current

Links

Landscapes

  • Adhesives Or Adhesive Processes (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)

Abstract

PURPOSE:To provide an aqueous emulsion adhesive to increase the adhesion of a vinyl chloride-based foam applied on the inner surface of a pottery tank for storing water for water closet. CONSTITUTION:This adhesive is prepared by mixing an aminated silane compound and an antifoaming agent with an aqueous emulsion of vinyl acetate polymer known in the prior art. Thereby, the water resistance is enhanced and the adhesiveness between the pottery surface of a water storage tank and a vinyl chloride foam is improved.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は陶磁器、特にシスタン内
側面に塩化ビニル系発泡体を施行する際に利用される接
着剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to ceramics, and more particularly to an adhesive used when a vinyl chloride foam is applied to the inner surface of a cistern.

【0002】[0002]

【従来技術の問題点】水洗トイレ用陶磁器貯水タンク
(シスタン)の結露防止対策として塩化ビニル系発泡体
層を設けることが行われている。塩化ビニル系発泡体層
を形成する手段には、予め形成された塩化ビニル系発泡
体層をシスタンの内面に接着する方法と、シスタンの内
面に塩化ビニル系発泡性ゾルを塗布し、加熱して発泡さ
せた層を形成する方法とが知られている。ところが近年
住宅の高級化傾向が強まると共にシスタンも箱形であっ
たのが形状が多様化して角部のないものが好まれるよう
になってきた。このような形状のシスタンにあっては内
面に塩化ビニル系発泡体層を設ける技術の高度化が要求
される。
[Problems of the prior art] As a measure for preventing dew condensation on a ceramic water storage tank (cistern) for flush toilets, a vinyl chloride foam layer has been provided. The means for forming the vinyl chloride foam layer includes a method of adhering a preformed vinyl chloride foam layer to the inner surface of the cistern and a method of applying the vinyl chloride foam sol to the inner surface of the cistern and heating it. Methods of forming a foamed layer are known. In recent years, however, as the trend toward higher-grade housing has increased, the cistern was also box-shaped, but the shape has diversified and it is becoming more and more preferred that there be no corners. In the case of a cistern having such a shape, it is required to improve the technique of providing a vinyl chloride foam layer on the inner surface.

【0003】一方、シスタンの内面と塩化ビニル系発泡
体層とは酢酸ビニル重合体系の水性エマルジョン系接着
剤を用いて接着させる。しかし酢酸ビニル重合体系の水
性エマルジョン系接着剤は耐水性が劣る欠点があるた
め、特に塩化ビニル系発泡性ゾルをシスタンの内面に塗
布し発泡体層を形成させる方法によった場合は、塩化ビ
ニル系発泡体層の剥離が生じやすい。
On the other hand, the inner surface of the cistern and the vinyl chloride foam layer are adhered to each other using an aqueous emulsion adhesive of vinyl acetate polymer type. However, since vinyl acetate polymer-based aqueous emulsion adhesives have the drawback of poor water resistance, vinyl chloride-based foaming sol is applied to the inner surface of the cistern to form a foam layer. Peeling of the foam layer tends to occur.

【0004】[0004]

【問題点の解決手段】そこで本発明においては前記酢酸
ビニル重合体系の水性エマルジョンに少量のアミノ基含
有シラン化合物を添加することにより常態における接着
性を向上させると共に耐水性を著しく改良できることを
見出した。
Therefore, in the present invention, it has been found that by adding a small amount of an amino group-containing silane compound to an aqueous emulsion of the vinyl acetate polymer, the adhesiveness in the normal state can be improved and the water resistance can be remarkably improved. ..

【0005】[0005]

【発明の構成】シスタンの内面に塩化ビニル系発泡性ゾ
ルの適用の前に接着剤、酢酸ビニル重合体系の水性エマ
ルジョンが塗布される。酢酸ビニル重合体系の水性エマ
ルジョンとしては酢酸ビニル重合体の他に酢酸ビニル−
エチレン共重合体の水性エマルジョンも使用されてい
る。塗布手段としては、ハケ塗りの他スプレー法による
がシスタンの形状が簡単な箱型以外の場合はスプレー法
によるのが便利である。水性エマルジョンを塗布したな
らば乾燥炉内で約150℃の温度に30分程度保持して
乾燥する。次いで塩化ビニル発泡性ゾルを厚さ約2mm程
度に塗布し熱風循環炉で通常は約150℃で10分間、
次いで昇温して約210℃で7分間程度加熱して発泡さ
せる。
DETAILED DESCRIPTION OF THE INVENTION An adhesive, an aqueous emulsion of vinyl acetate polymer, is applied to the inner surface of a cistern before application of a vinyl chloride foamable sol. Aqueous emulsions of vinyl acetate polymer include vinyl acetate-
Aqueous emulsions of ethylene copolymers have also been used. As a coating method, it is convenient to use a spray method in addition to a brush coating method, but to use a spray method if the shape of the stan is not a simple box type. Once the aqueous emulsion has been applied, it is dried by holding it at a temperature of about 150 ° C. for about 30 minutes in a drying oven. Next, a vinyl chloride foaming sol is applied to a thickness of about 2 mm, and it is usually heated at about 150 ° C. for 10 minutes in a hot air circulation oven.
Then, the temperature is raised to about 210 ° C. for about 7 minutes for foaming.

【0006】本発明で使用する酢酸ビニル重合体系水性
エマルジョンはエスダイン6040(積水化学工業株式
会社)、SP−210(コニシ株式会社)あるいはBE
−800(中央理化工業株式会社)等の名称で市販され
ている。これは固形分濃度が50〜60%程度であり、
約7〜12倍の水で希釈して用いるのが便利である。本
発明ではこれにアミノ基含有シラン化合物を全組成物当
たり0.2〜5重量%添加する。アミノ基含有化合物は
塩基性(約 pH10.5)であり、前記酢酸ビニル重合体
系水性エマルジョンのpHは4〜6、多くは5〜5.5で
あるためシラン化合物の添加により水性エマルジョンの
安定性が低下し塗布特にスプレーによる塗布を困難にす
ることがある。このような場合には少量の界面活性剤を
添加すればよい。界面活性剤としてはHLB値の大きい
ノニオン系界面活性剤、例えばHLB値が約15以上で
あるポリオキシエチレンソルビタン脂肪酸エステル、ポ
リオキシエチレンアルキルエーテル、ポリオキシエチレ
ンアルキルアリールエーテルを添加するのが好ましい。
界面活性剤の使用量は水性エマルジョンの固形分100
重量部あたり0.5〜2重量部であって、多量に使用す
ると耐水性を低下させることになり好ましくない。
The vinyl acetate polymer aqueous emulsion used in the present invention is Esdyne 6040 (Sekisui Chemical Co., Ltd.), SP-210 (Konishi Co., Ltd.) or BE.
It is commercially available under the names such as -800 (Chuo Rika Kogyo Co., Ltd.). This has a solid content of about 50-60%,
It is convenient to use by diluting with about 7 to 12 times water. In the present invention, an amino group-containing silane compound is added thereto in an amount of 0.2 to 5% by weight based on the total composition. Since the amino group-containing compound is basic (about pH 10.5), and the pH of the vinyl acetate polymer-based aqueous emulsion is 4 to 6, most of which is 5 to 5.5, the stability of the aqueous emulsion is improved by adding the silane compound. May decrease, which may make application, particularly spray application, difficult. In such a case, a small amount of surfactant may be added. As the surfactant, it is preferable to add a nonionic surfactant having a large HLB value, for example, a polyoxyethylene sorbitan fatty acid ester, a polyoxyethylene alkyl ether, or a polyoxyethylene alkyl aryl ether having an HLB value of about 15 or more.
The amount of surfactant used is 100% solid content of the aqueous emulsion.
It is 0.5 to 2 parts by weight per part by weight, and it is not preferable to use a large amount because the water resistance is lowered.

【0007】本発明で用いられるアミノ基含有シラン化
合物としてはいかなるものでもよいが、N−(βアミノ
エチル)−γ−アミノプロピルトリメトキシシランが最
も有効であり、かつ入手容易であって好ましい。そのよ
うなシラン化合物は信越シリコーン製「KBM−60
3」あるいは東芝シリコーン製「TSL−8340」と
して市販されている。アミノ基含有シラン化合物の使用
量が0.2重量%以下であると接着性の向上がみられ
ず、また5重量%を大きく超えると塩化ビニル発泡性ゾ
ルの発泡が異常となるので好ましくない。またスプレー
塗布中バックプレッシャー等により著しい泡立ち現象が
起こり均一な塗布が困難になることもあるがそのような
場合には約0.05〜1重量%の消泡剤を加えるとよ
く、シリコーンオイル系の消泡剤が好適である。さらに
必要に応じて染料、香料等を加え得ることは当然であ
る。
Although any amino group-containing silane compound may be used in the present invention, N- (βaminoethyl) -γ-aminopropyltrimethoxysilane is the most effective and preferred because it is easily available. Such a silane compound is manufactured by Shin-Etsu Silicone “KBM-60
3 ”or“ TSL-8340 ”manufactured by Toshiba Silicone. When the amount of the amino group-containing silane compound used is 0.2% by weight or less, the adhesiveness is not improved, and when it exceeds 5% by weight, the foaming of the vinyl chloride foaming sol becomes abnormal, which is not preferable. In addition, there is a case where a remarkable foaming phenomenon occurs due to back pressure during spray application, which makes uniform application difficult. In such a case, it is advisable to add about 0.05 to 1% by weight of an antifoaming agent. The defoaming agent of is preferable. Further, it goes without saying that dyes, fragrances and the like can be added if necessary.

【0008】次に実施例および比較例をあげ本発明をよ
り具体的に説明する。 塩化ビニル発泡性ゾルの配合 重量部 G−22(日本ゼオン) 100 51 DOP 85 43.4 PVC安定剤,FL-64(Ba-Zn系,旭電化工業) 4 2 セル調整剤,KH−300A−10 1 0.5 発泡剤,AZ−H(大塚化学) 6 3.1
Next, the present invention will be described more concretely with reference to Examples and Comparative Examples. Compounding parts by weight of vinyl chloride foaming sol % G-22 (Nippon Zeon) 100 51 DOP 85 43.4 PVC stabilizer, FL-64 (Ba-Zn system, Asahi Denka Co., Ltd.) 42 Cell modifier, KH-300A -10 1 0.5 Foaming agent, AZ-H (Otsuka Chemical) 6 3.1

【0009】接着剤の調製 表1に示す各成分の相当量(重量部)を以下の順序で小
型撹拌機(新東化学製,スリーワンモーター)にて混合
(各添加毎に30秒程度)。 使用材料 アミノ基含有シラン化合物(信越化学製:KBM−60
3,pH10.5)、消泡剤(信越化学製:KM−7
1)、界面活性剤(ポリオキシエチレンラウリルエーテ
ル系ノニオン界面活性剤,花王製:エマルゲン120,
HLB 15.3)および酢酸ビニル−エチレン共重合体
水性エマルジョン(積水化学製:エスダイン6040,
pH5.5,固形分濃度56%) 〔添加順序〕水、KBM−603、KM−71、エマル
ゲン120、エスダイン6040。但しエマルゲン12
0は等重量の水で希釈して使用。
Preparation of Adhesives The corresponding amounts (parts by weight) of the respective components shown in Table 1 were mixed in the following order with a small stirrer (manufactured by Shinto Kagaku, Three One Motor) (about 30 seconds for each addition). Materials used Amino group-containing silane compound (manufactured by Shin-Etsu Chemical: KBM-60
3, pH 10.5), antifoaming agent (manufactured by Shin-Etsu Chemical: KM-7)
1), surfactant (polyoxyethylene lauryl ether-based nonionic surfactant, manufactured by Kao: Emulgen 120,
HLB 15.3) and vinyl acetate-ethylene copolymer aqueous emulsion (Sekisui Chemical Co., Ltd .: Esdyne 6040,
pH 5.5, solid content concentration 56%) [Order of addition] Water, KBM-603, KM-71, Emulgen 120, Esdyne 6040. However, Emulgen 12
0 is diluted with an equal weight of water before use.

【0010】評価方法 (1) 長時間加熱接着性 任意の大きさのシスタン内側面(艶無し面)に水系接着
剤をスプレー塗布し、熱風循環炉にて長時間加熱(15
0℃×0.5〜48時間)後、塩化ビニル系発泡性ゾル
を塗布(厚さ約2mm)。暫時、熱風循環炉にて二段加熱
発泡{(150℃×10分)+(210℃×7分)}を施
し、長時間加熱接着性を0.5、1、24および48時
間毎に評価した。
Evaluation method (1) Long-term heating adhesiveness A water-based adhesive is spray-coated on the inner surface (matte surface) of a cistern of arbitrary size, and heated for a long time in a hot air circulation furnace (15
After 0 ° C for 0.5 to 48 hours), a vinyl chloride foaming sol is applied (thickness: about 2 mm). Temporarily, two-stage heating foaming {(150 ° C × 10 minutes) + (210 ° C × 7 minutes)} was applied in a hot air circulation furnace, and long-term heat adhesion was evaluated every 0.5, 1, 24 and 48 hours. did.

【0011】(2) 耐水接着性 上記(1)で得られた発泡試片を水に浸漬し(25℃×3
〜6ケ月)、経過後の耐水接着性を評価した。但し(1)
における長時間加熱は150℃×48時間とした。
(2) Water-resistant adhesiveness The foamed test piece obtained in the above (1) is immersed in water (25 ° C. × 3).
~ 6 months), the water-resistant adhesive property after the elapse was evaluated. However (1)
The long time heating at 150 ° C. for 48 hours was performed.

【0012】(3) 接着剤の経時安定性 調整した接着剤を恒温湿室に放置し(25℃×60%R
H×30日)上記(1)および(2)の試験を行った。但し
(1)における長時間加熱は150℃×24時間とした。
また(2)における水浸漬は25℃×3ケ月とした。
(3) Stability of adhesive with time The adjusted adhesive is left in a constant temperature and humidity chamber (25 ° C. × 60% R
H × 30 days) The tests (1) and (2) above were performed. However
The long-time heating in (1) was 150 ° C. × 24 hours.
The water immersion in (2) was performed at 25 ° C. for 3 months.

【0013】(4) 接着性評価方法 上記(1)、(2)、(3)で得られた各試片のシスタン/発
泡体層間を鋭利なナイフにて切開し、接着の難・易を判
断した。
(4) Adhesiveness Evaluation Method The cistern / foam layer of each of the samples obtained in (1), (2) and (3) above is cut with a sharp knife to make the adhesion difficult and easy. It was judged.

【0014】(5) 発泡体表面状態 上記各条件で得られたシスタン発泡体の表面発泡状態を
肉眼観察した。
(5) Surface state of foamed body The surface foamed state of the Cistern foam obtained under each of the above conditions was visually observed.

【0015】(6) スプレー塗布性 スプレーガン(IWATA製:W−61タイプ,ノズル径1m
m,空気圧3kgf/cm2)にて、表1記載の各接着剤をシ
スタン内側面に塗布した時の塗布の難・易を評価した。 〔評価基準〕 (1) 均一性(エマルジョンの凝集によるノズルの目詰ま
り、粘度上昇等と関連) (2) 泡立ち
(6) Spray coatability Spray gun (made by IWATA: W-61 type, nozzle diameter 1 m
At m and air pressure of 3 kgf / cm 2 ), the difficulty and easiness of application when each adhesive listed in Table 1 was applied to the inner surface of the cistern was evaluated. [Evaluation criteria] (1) Uniformity (related to nozzle clogging due to emulsion aggregation, viscosity increase, etc.) (2) foaming

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【表2】 [Table 2]

【0018】表2の結果から酢酸ビニル重合体系水性エ
マルジョンからなる接着剤のみでは耐水接着性が劣り、
シスタンと発泡体との界面に水が浸入し、シスタン表面
の結露を防止するためにシスタンの内面に発泡体層を設
けたとの本来の目的を満足しないことになり、またアミ
ノ基含有シラン化合物のみでも長時間加熱接着性が劣
り、前記結露防止対策として不適当であることがわか
る。ところが本発明の接着剤によれば、耐水性、長時間
加熱安定性が優れた接着ができ、またスプレー塗布も可
能である。
From the results shown in Table 2, the water-resistant adhesiveness was inferior only with the adhesive composed of the vinyl acetate polymer-based aqueous emulsion.
Water infiltrates into the interface between the cistern and the foam, and the original purpose of providing a foam layer on the inside of the cistern to prevent condensation on the surface of the stan is not satisfied, and only the amino group-containing silane compound is used. However, it was found that the adhesiveness against heating by heat for a long time was inferior and it was unsuitable as the above-mentioned measure for preventing dew condensation. However, according to the adhesive of the present invention, it is possible to carry out adhesion having excellent water resistance and long-term heating stability, and spray application is also possible.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 アミノ基を含有するシラン化合物および
消泡剤を含有する酢酸ビニル重合体系の水性エマルジョ
ンからなる塩化ビニル系発泡体と陶磁器との接着剤。
1. An adhesive between a vinyl chloride type foam comprising an aqueous emulsion of a vinyl acetate polymer containing an silane compound having an amino group and an antifoaming agent and a ceramic.
JP10300592A 1992-04-22 1992-04-22 Aqueous emulsion adhesive Pending JPH05295338A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10300592A JPH05295338A (en) 1992-04-22 1992-04-22 Aqueous emulsion adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10300592A JPH05295338A (en) 1992-04-22 1992-04-22 Aqueous emulsion adhesive

Publications (1)

Publication Number Publication Date
JPH05295338A true JPH05295338A (en) 1993-11-09

Family

ID=14342550

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10300592A Pending JPH05295338A (en) 1992-04-22 1992-04-22 Aqueous emulsion adhesive

Country Status (1)

Country Link
JP (1) JPH05295338A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08188764A (en) * 1995-01-06 1996-07-23 Sunstar Eng Inc Two liquid crosslinking type aqueous adhesive

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08188764A (en) * 1995-01-06 1996-07-23 Sunstar Eng Inc Two liquid crosslinking type aqueous adhesive

Similar Documents

Publication Publication Date Title
JP4467105B2 (en) Use of emulsifying silane coupling agents as primers to improve the adhesion of sealants, adhesives and coatings
JP3353300B2 (en) Aqueous silane adhesive composition
US4106948A (en) Aqueous compositions
EP0209067B1 (en) Alpha-cyanoacrylate adhesive composition of matter
JPH06316473A (en) Dissipating aging and coating composition for concrete
JP2001515117A (en) Double-curable silicone composition
JPH05295338A (en) Aqueous emulsion adhesive
US4578407A (en) Thixotropic rust removal coating and process
JPH04504433A (en) Polymeric aqueous compositions for protective coatings
JP3353621B2 (en) Fluorinated resin aqueous dispersion composition
JPH07166066A (en) One-component nonsolvent conformal coating
JPH1112544A (en) Primer composition
JPS619463A (en) Coating agent for inorganic building material
JP2922416B2 (en) Primer composition
JP2884093B2 (en) Polymer aqueous dispersion composition
US3455762A (en) Methods of bonding silicone rubbers to surfaces
JP2003171157A5 (en)
WO2019032168A1 (en) Natural stone sealer compositions
JP2001152116A (en) Aqueous adhesive
JPH08209060A (en) Cold drying aqueous emulsion-based coating material
JPS5840365A (en) Coating composition
JP2003213208A (en) Method for forming pollution-resistant coated film and coating material composition
JP3444993B2 (en) Coating material composition for forming a coating film applied on an underground building
JPH01126243A (en) Composition for covering cut of wired sheet glass
JPS6389572A (en) Paint composition for pvc cloth