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JPS6255559B2 - - Google Patents
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JPS6255559B2 - - Google Patents

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Publication number
JPS6255559B2
JPS6255559B2 JP55084075A JP8407580A JPS6255559B2 JP S6255559 B2 JPS6255559 B2 JP S6255559B2 JP 55084075 A JP55084075 A JP 55084075A JP 8407580 A JP8407580 A JP 8407580A JP S6255559 B2 JPS6255559 B2 JP S6255559B2
Authority
JP
Japan
Prior art keywords
viscosity
adhesive composition
temperature
storage stability
cps
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
Application number
JP55084075A
Other languages
Japanese (ja)
Other versions
JPS5710665A (en
Inventor
Yorinobu Ikeda
Tadayoshi Nakajima
Atsushi Ichikawa
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.)
JSR Corp
Original Assignee
Japan Synthetic Rubber Co Ltd
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 Japan Synthetic Rubber Co Ltd filed Critical Japan Synthetic Rubber Co Ltd
Priority to JP8407580A priority Critical patent/JPS5710665A/en
Publication of JPS5710665A publication Critical patent/JPS5710665A/en
Publication of JPS6255559B2 publication Critical patent/JPS6255559B2/ja
Granted legal-status Critical Current

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  • Adhesives Or Adhesive Processes (AREA)
  • Manufacturing Of Multi-Layer Textile Fabrics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は放置安定性、耐ブリスター性の優れた
カーペツト裏打用接着剤組成物の製造方法に関す
る。 近年カーペツト裏打加工において、乾燥速度を
上げるためにドライヤの乾燥温度を上げる傾向が
強い。しかしながらこのような乾燥温度上昇によ
る乾燥速度の向上は反面ブリスター(火ぶくれ)
現象という好ましくない現象をもたらす。この現
象は接着剤層の表面に乾燥時皮膜が形成され、そ
の皮膜を内部の水蒸気が持ち上げるために発生す
るものである。最近カーペツトの加工技術の変化
により、通気性の悪いポリプロピレンを一次バツ
キング材に用いたり、パイルにナイロンを用いた
りするようになり、このためブリスター現象は
益々発生し易くなつてきている。この現象のため
に結局ドライヤの乾燥温度を上げることができな
いという矛盾が起る。従つて乾燥温度上昇による
生産性を向上させるには耐ブリスター性の良好な
接着剤組成物の開発が不可欠である。 従来この耐ブリスター性の良好な接着剤を得る
方法として種々の技術が公知であるが、ブリスタ
ー発生機構の本質からして特に感熱増粘性を利用
した方法が最も有利であると考えられる(例えば
特開昭52―95749、特開昭54―126242、特開昭50
―139136など)。またこのような感熱増粘または
ゲル化するための方法は上記特許のほか特公昭45
―26978、特公昭47―19604、特公昭40―21427等
ですでに知られている。しかしながらこれらの方
法でも使用条件によつては接着剤組成物の高温で
の放置安定性が悪くなる場合が多い。特にカーペ
ツトの加工業者がすでに感熱化されたラテツクス
組成物を用いて接着剤組成物を製造する場合、こ
の接着剤組成物の放置安定性のほかに貯蔵時のラ
テツクス組成物の放置安定性も同時に要求され
る。 このように耐ブリスター性と放置安定性、特に
高温時の放置安定性の両方を同時に満足させるこ
とは困難であるが、高温時の放置安定性の悪いも
のでも増粘する温度以下で貯蔵すれば特に問題は
ないが、積極的に耐ブリスター性と高温時の放置
安定性の両方を満足させるものが望まれている。 そこで本発明者らは耐ブリスター性が良好で且
つ高温度の放置安定性にも優れた接着剤組成物を
得る目的から配合処方等を種々鋭意検討した結
果、配合剤を添加したときの接着剤組成物の粘度
の温度依存性が一定の条件を満たすとき全く驚く
べきことに耐ブリスター性と高温時の放置安定性
が同時に満足する良好な接着剤組成物が得られる
ことを見出し本発明に到達した。すなわち本発明
は天然ゴムまたは合成ゴムラテツクス或いは樹脂
エマルジヨン(以下ラテツクス等と略称する)に
充填剤、増粘剤および感熱性を有する添加剤を含
有させた接着剤組成物において、該組成物の60℃
未満における粘度がBM型粘度計6rpmで測定して
10000〜40000cpsで且つ60〜100℃の温度領域に
おける任意の到達点温度での粘度が120秒以内に
100000cps以上に増粘するように添加剤を配合す
ることを特徴とする放置安定性、耐ブリスター性
良好なカーペツト裏打用接着剤組成物の製造方法
である。 以下に本発明を詳細に説明する。 本発明に使用するラテツクス等は天然ゴム、ス
チレン―ブタジエンゴムラテツクス、カルボキシ
変性スチレン―ブタジエンゴムラテツクス、アク
リロニトリル―ブタジエンラテツクス等の合成ゴ
ムラテツクスおよびアクリルエマルジヨン、塩化
ビニルエマルジヨン、エチレン―酢酸ビニルエマ
ルジヨン等の樹脂エマルジヨン等一般にカーペツ
トバツキングに用いられるもののすべてのラテツ
クスを指す。 本発明に使用される充填剤、増粘剤はカーペツ
トバツキング用接着剤組成物を構成する添加剤と
して使用されるもので、これ以外にも顔料、分散
剤、消泡剤、可塑剤、老化防止剤等をも含めるこ
とができる。 さらに本発明に用いられる感熱性を有する添加
剤とは一般に感熱ゲル化剤と称せられるポリアル
キレンオキサイド、ポリエーテルポリホルマー
ル、ポリビニルメチルエーテル、ポリアルキレン
オキサイド変性ポリシロキサン等のほか、水溶性
ポリアミド、デンプン、メチルセルローース、卵
タンパク等の感熱性を有する増粘剤、ポリリン酸
塩および曇点を有するノニオン乳化剤等を添加し
たときにみられるようにある温度において構造、
機能が変化しラテツクスおよびラテツクス組成物
の性質に変化を与えるような添加剤のすべてを意
味する。本発明においては同時に上記添加剤と併
用することにより感熱温度、増粘性に変化を与え
るアンモニア、ホウ酸塩、亜鉛華、尿素その他多
価金属の塩、複塩、錯塩等の感熱助剤およびノニ
オン、アニオン乳化剤の如き安定剤も感熱性を有
する添加剤の中に含まれる。 本発明における感熱性を有する添加剤は以下に
示すように粘度が温度依存性を示すように配合さ
れる。すなわち接着剤組成物の粘度が60〜100
℃、好ましくは60〜80℃の温度領域におけるある
温度で、120秒以内、好ましくは60秒以内にBM
型粘度計6rpmで測定して100000cps以上に増粘す
るように配合する。かかる粘度の温度依存性はラ
テツクスの種類、配合する感熱性を有する添加剤
の種類によつて異なるのでその添加量は一律に決
められない。 感熱性添加剤として好ましい化合物およびその
添加量(ラテツクス固形分100重量部に対する重
量部)は、ポリアルキレンオキサイド0.5〜15、
好ましくは1〜7、ポリエーテルポリホルマー
ル、ポリビニルメチルエーテル、およびポリアル
キレンオキサイド変性ポリシロキサン0.1〜10、
好ましくは0.5〜5、水溶性ポリアミド0.5〜20、
好ましくは1〜10、デンプン1〜30、好ましくは
5〜20である。 添加剤と併用するアンモニア、ホウ酸塩、亜鉛
華、尿素その他多価金属の塩、複塩、錯塩などは
0.05〜10、好ましくは0.3〜5、ノニオン、アニ
オン乳化剤は0.05〜5、好ましくは0.1〜3であ
る。 増粘をはじめる温度が60℃未満の場合には夏期
等比較的高温で保存する必要がある場合に該組成
物の安定性が悪くなり実用的でない。一方増粘開
始温度が100℃を越える場合には満足な耐ブリス
ター性が得られない。増粘したときの粘度が
100000cps以下の場合にも同様に満足な耐ブリス
ター性が得られない。また増粘に要する時間が
120秒を越えるとブリスターが発生する。 従つて本発明の如く60℃未満の粘度が10000〜
40000cpsである接着剤組成物に感熱性を有する
添加剤を配合して60〜100℃の温度領域における
任意の到達点温度で120秒以内に100000cps以上
の粘度となる接着剤組成物が良好な放置安定性、
耐ブリスター性を与える。ここで任意の到達点温
度とはブリスターが発生する温度以下で、増粘さ
せたい温度であり、カーペツトの乾燥条件により
設定される。 次に実施例を挙げて本発明を具体的に説明す
る。 用いた配合および評価法を以下に示す。 (1) 配合 ラテツクス *1 100重量部(固形分) 充 填 剤 *2 350重量部 増 粘 剤 *3 適量 により次のように調整する。 固 形 分 75% 粘 度 26000cps(BM型6rpm) この接着剤組成物に表1に示す各種感熱性を有
する添加剤を配合する。 *1 カルボキシ変性スチレン―ブタジエンラ
テツクス 日本合成ゴム製〓0593 *2 炭酸カルシウム 日東粉化製 SS30 *3 ポリアクリル酸ソーダ 東亜合成製
A20P (2) 評価法 耐ブリスター性 シユバングヒーター(リンナイ社製) ガ ス 圧 280mm水柱 基布までの距離 15cm 原 反 20m×15cm 一次基布 PP パイル ナイロン 塗 布 量 1.3Kg/m2 ブリスター評価方法 前記原反に前記量の接着剤組成物をガラス
棒、ゴムヘラ等を用いて手早く均一に拡げ塗布
する。塗布された原反を通気性の良い金網の上
にのせ、前記条件のシユバングヒータの下に置
き3分間乾燥させる。発生した火ぶくれの数を
かぞえて次の基準に従つて判定する。 基 準 5 級 火ぶくれ皆無 4 級 火ぶくれ総数10コ以下 3 級 火ぶくれ総数30コ以下 2 級 火ぶくれ総数50コ以下 1 級 全面火ぶくれ 放置安定性 恒温槽内でBM型粘度計6rpmで測定する。 基 準 ○ 60℃ 一週間以上で変化なし △ 60℃ 一日以上で増粘、ゲル化 × 60℃ 一日以下で増粘、ゲル化 実施例1〜3、比較例1〜4 ポリアルキレンオキサイド変性ポリシロキサン
として曇点35℃のポリアルキレンオキサイド変性
ポリシロキサン(A)、曇点75℃のポリアルキレンオ
キサイド変性ポリシロキサン(B)および非感熱性ポ
リアルキレンオキサイド変性ポリシロキサン(C)の
3種とその他表1に掲げる感熱性を有する添加剤
を用い、前記に示した接着剤組成物の配合時の粘
度を26000cpsとして各温度域での粘度が表1に
示す通り粘度が変化するよう配合条件を変え7種
類の接着剤組成物を得た。 得られた組成物の粘度の温度依存性と耐ブリス
ター性および放置安定性の結果を表1に示す。 表1の結果から60℃未満における粘度が
40000cpsを超える場合、耐ブリスター性の良い
場合があるが、組成物の放置安定性が悪い(比較
例1、2)。また60〜100℃の温度領域における急
激な粘度上昇を伴なわない組成物(比較例4)お
よび100℃を超えた温度で急激に増粘するような
組成物(比較例3)の場合、耐ブリスター性は全
く改良されないことがわかる。また急激に増粘す
る温度が80℃以上の場合、耐ブリスター性は完全
には改良されない(実施例2)。 実施例4、5 比較例5、6 糊化温度60〜70℃の生バレイシヨデンプンおよ
び糊化温度80〜90℃の生トウモロコシデンプンと
ホウ砂を用いて前記に示した接着剤組成物の配合
時の粘度を26000cpsとして、各温度域での粘度
が表2に示す通り変化するように配合条件を変え
4種類の接着剤組成物を得た。得られた組成物の
温度依存性と耐ブリスター性および放置安定性を
表2に示す。 生バレイシヨデンプンは糊化したときの粘度が
高いため耐ブリスター性は良好であり、また放置
安定性もよい(実施例4)。生トウモロコシデン
プンの場合、糊化温度が高く糊化したときの粘度
が低いため放置安定性はよいが、耐ブリスター性
は悪い(比較例6)。そこでホウ砂の如き糊化し
た場合の粘度を上げるような添加剤を加えること
により放置安定性はそのまま良好で且つ耐ブリス
ター性の良好な組成物が得られた(実施例5)。
The present invention relates to a method for producing an adhesive composition for carpet lining which has excellent storage stability and blister resistance. In recent years, there has been a strong trend in carpet lining processing to increase the drying temperature of the dryer in order to increase the drying speed. However, this increase in drying temperature does not improve the drying speed, but on the other hand, it may cause blistering.
bring about an undesirable phenomenon. This phenomenon occurs because a film is formed on the surface of the adhesive layer when it dries, and the film is lifted by the internal water vapor. Recent changes in carpet processing technology have led to the use of polypropylene, which has poor air permeability, as the primary backing material and the use of nylon for the pile, making the blister phenomenon more likely to occur. This phenomenon results in a contradiction in that the drying temperature of the dryer cannot be increased. Therefore, in order to improve productivity by increasing drying temperature, it is essential to develop an adhesive composition with good blister resistance. Conventionally, various techniques have been known to obtain adhesives with good blister resistance, but considering the nature of the blister generation mechanism, a method that utilizes heat-sensitive thickening properties is considered to be the most advantageous (for example, 1977-95749, 1977-126242, 1977-126242, 1972
-139136 etc.). In addition to the above-mentioned patent, the method for heat-sensitive thickening or gelling is disclosed in Japanese Patent Publication No. 45
-26978, Special Publication No. 47-19604, Special Publication No. 40-21427, etc. are already known. However, even with these methods, depending on the conditions of use, the storage stability of the adhesive composition at high temperatures often deteriorates. Particularly when a carpet processor manufactures an adhesive composition using a latex composition that has already been heat-sensitized, in addition to the storage stability of this adhesive composition, the storage stability of the latex composition during storage is also important. required. In this way, it is difficult to satisfy both blister resistance and storage stability, especially storage stability at high temperatures, at the same time, but even products with poor storage stability at high temperatures can be stored below the temperature at which they thicken. Although there are no particular problems, it is desirable to have a material that positively satisfies both blister resistance and storage stability at high temperatures. Therefore, the present inventors conducted extensive studies on various formulations, etc. with the aim of obtaining an adhesive composition with good blister resistance and excellent storage stability at high temperatures. The inventors have surprisingly discovered that when the temperature dependence of the viscosity of the composition satisfies certain conditions, a good adhesive composition can be obtained that simultaneously satisfies blister resistance and storage stability at high temperatures, leading to the present invention. did. That is, the present invention relates to an adhesive composition in which natural rubber or synthetic rubber latex or resin emulsion (hereinafter referred to as latex) contains a filler, a thickener, and a heat-sensitive additive.
The viscosity below is measured with a BM type viscometer at 6 rpm.
Viscosity within 120 seconds at any desired point temperature in the temperature range of 10,000 to 40,000 cps and 60 to 100℃
This is a method for producing an adhesive composition for carpet lining having good storage stability and blister resistance, which is characterized by blending additives so as to increase the viscosity to 100,000 cps or more. The present invention will be explained in detail below. Latexes used in the present invention include natural rubber, synthetic rubber latex such as styrene-butadiene rubber latex, carboxy-modified styrene-butadiene rubber latex, acrylonitrile-butadiene latex, and acrylic emulsion, vinyl chloride emulsion, and ethylene-vinyl acetate. Refers to all latexes commonly used for carpet backing, such as resin emulsions such as emulsions. The fillers and thickeners used in the present invention are used as additives constituting the adhesive composition for carpet backing. Antiaging agents and the like may also be included. Furthermore, the heat-sensitive additives used in the present invention include polyalkylene oxide, polyether polyformal, polyvinyl methyl ether, polyalkylene oxide-modified polysiloxane, etc., which are generally called heat-sensitive gelling agents, as well as water-soluble polyamide and starch. structure at a certain temperature, as seen when adding heat-sensitive thickeners such as methylcellulose, egg protein, polyphosphates, nonionic emulsifiers with cloud points, etc.
It refers to all additives whose function changes and which alter the properties of latexes and latex compositions. In the present invention, heat-sensitive auxiliaries such as ammonia, borates, zinc white, urea, and other polyvalent metal salts, double salts, and complex salts, which change the heat-sensitive temperature and thickening properties when used in combination with the above additives, and nonions Stabilizers such as , anionic emulsifiers are also included among the heat-sensitive additives. The heat-sensitive additive in the present invention is blended so that its viscosity exhibits temperature dependence as shown below. That is, the viscosity of the adhesive composition is 60-100
BM within 120 seconds, preferably within 60 seconds at a certain temperature in the temperature range of ℃, preferably 60-80℃
Blend so that the viscosity increases to 100,000 cps or more when measured with a type viscometer at 6 rpm. The temperature dependence of viscosity varies depending on the type of latex and the type of heat-sensitive additive to be blended, so the amount to be added cannot be determined uniformly. Preferred compounds and amounts added as heat-sensitive additives (parts by weight relative to 100 parts by weight of latex solid content) are polyalkylene oxide 0.5 to 15;
Preferably 1 to 7, polyether polyformal, polyvinyl methyl ether, and polyalkylene oxide modified polysiloxane 0.1 to 10,
Preferably 0.5-5, water-soluble polyamide 0.5-20,
Preferably it is 1-10, starch 1-30, preferably 5-20. Salts, double salts, complex salts, etc. of ammonia, borates, zinc white, urea, and other polyvalent metals used together with additives are
0.05-10, preferably 0.3-5, nonionic and anionic emulsifiers 0.05-5, preferably 0.1-3. If the temperature at which viscosity starts to thicken is less than 60°C, the stability of the composition deteriorates when it is necessary to store it at a relatively high temperature such as in summer, making it impractical. On the other hand, if the thickening start temperature exceeds 100°C, satisfactory blister resistance cannot be obtained. The viscosity when thickened is
Similarly, satisfactory blister resistance cannot be obtained when the amount is less than 100,000 cps. Also, the time required for thickening
If it exceeds 120 seconds, blistering will occur. Therefore, as in the present invention, the viscosity below 60℃ is 10,000~
Adhesive compositions that have a viscosity of 100,000 cps or more within 120 seconds at any desired temperature in the temperature range of 60 to 100°C by blending a heat-sensitive additive with an adhesive composition that has a viscosity of 40,000 cps are considered to have good storage properties. Stability,
Provides blister resistance. Here, the arbitrary target temperature is a temperature at which viscosity is desired to be increased, which is below the temperature at which blistering occurs, and is set according to the drying conditions of the carpet. Next, the present invention will be specifically explained with reference to Examples. The formulation and evaluation method used are shown below. (1) Compound Latex *1 100 parts by weight (solid content) Filler *2 350 parts by weight Thickener *3 Adjust the appropriate amount as follows. Solid content 75% Viscosity 26000 cps (BM type 6 rpm) Various heat-sensitive additives shown in Table 1 are blended into this adhesive composition. *1 Carboxy-modified styrene-butadiene latex manufactured by Nippon Synthetic Rubber Co., Ltd. 0593 *2 Calcium carbonate manufactured by Nitto Funka Co., Ltd. SS30 *3 Sodium polyacrylate manufactured by Toagosei Co., Ltd.
A20P (2) Evaluation method Blister resistance Shubang heater (manufactured by Rinnai) Gas pressure 280mm water column Distance to base fabric 15cm Raw fabric 20m x 15cm Primary base fabric PP pile Nylon Coating amount 1.3Kg/m 2 Blister evaluation method The adhesive composition in the above amount is quickly and uniformly spread and applied onto the original fabric using a glass rod, a rubber spatula, or the like. The coated original fabric was placed on a well-ventilated wire gauze, placed under a swiveling heater under the above conditions, and dried for 3 minutes. Count the number of blisters that occur and judge according to the following criteria. Criteria Grade 5 No blisters Grade 4 Total number of blisters 10 or less Grade 3 Total number of blisters 30 or less Grade 2 Total number of blisters 50 or less Grade 1 Full-face blisters Storage stability BM type in a thermostatic chamber Measure with a viscometer at 6 rpm. Criteria ○ 60℃ No change after one week or more △ 60℃ Thickening and gelation after one day × 60℃ Thickening and gelation after one day or less Examples 1 to 3, Comparative Examples 1 to 4 Polyalkylene oxide modification There are three types of polysiloxane: polyalkylene oxide-modified polysiloxane (A) with a cloud point of 35°C, polyalkylene oxide-modified polysiloxane (B) with a cloud point of 75°C, and non-heat-sensitive polyalkylene oxide-modified polysiloxane (C), and others. Using the heat-sensitive additives listed in Table 1, the viscosity at the time of compounding the adhesive composition shown above was 26,000 cps, and the compounding conditions were changed so that the viscosity at each temperature range changed as shown in Table 1. Seven types of adhesive compositions were obtained. Table 1 shows the results of the temperature dependence of viscosity, blister resistance, and storage stability of the obtained composition. From the results in Table 1, the viscosity below 60℃ is
When it exceeds 40,000 cps, the blister resistance may be good, but the storage stability of the composition is poor (Comparative Examples 1 and 2). In addition, in the case of a composition that does not have a rapid viscosity increase in the temperature range of 60 to 100°C (Comparative Example 4) and a composition that rapidly thickens at a temperature exceeding 100°C (Comparative Example 3), It can be seen that the blister properties are not improved at all. Furthermore, when the temperature at which the viscosity rapidly increases is 80°C or higher, the blister resistance is not completely improved (Example 2). Examples 4 and 5 Comparative Examples 5 and 6 Formulation of the adhesive composition shown above using raw potato starch with a gelatinization temperature of 60 to 70°C and raw corn starch and borax with a gelatinization temperature of 80 to 90°C Four types of adhesive compositions were obtained by changing the compounding conditions so that the viscosity at each temperature range varied as shown in Table 2, with the viscosity at 26,000 cps. Table 2 shows the temperature dependence, blister resistance, and storage stability of the obtained composition. Since raw potato starch has a high viscosity when gelatinized, it has good blister resistance and good storage stability (Example 4). In the case of raw corn starch, the gelatinization temperature is high and the viscosity when gelatinized is low, so the storage stability is good, but the blister resistance is poor (Comparative Example 6). Therefore, by adding an additive such as borax that increases the viscosity when gelatinized, a composition with good storage stability and good blister resistance was obtained (Example 5).

【表】【table】

【表】【table】

【表】 実施例6、比較例7 コンパウンド配合を表3のとおりにした以外
は、実施例1と同様にして配合し、評価した。比
較例7は従来技術によるものであるが、60〜100
℃の温度領域で120秒以内に100000cps以上にな
らず、耐ブリスター性が十分でなかつた。
[Table] Example 6, Comparative Example 7 Compounds were blended and evaluated in the same manner as in Example 1, except that the compound formulation was as shown in Table 3. Comparative example 7 is based on the conventional technology, but the 60 to 100
It did not reach 100,000 cps or more within 120 seconds in the temperature range of °C, and the blister resistance was insufficient.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 天然ゴムまたは合成ゴムラテツクス或いは樹
脂エマルジヨン(以下ラテツクス等と略称する)
に充填剤、増粘剤および感熱性を有する添加剤を
含有させた接着剤組成物において、該組成物の60
℃未満における粘度がBM型粘度計6rpmで測定し
て10000〜40000cpsで、且つ60〜100℃の温度領
域における任意の到達点温度での粘度が120秒以
内に100000cps以上に増粘するように添加剤を配
合することを特徴とする放置安定性、耐ブリスタ
ー性良好なカーペツト裏打用接着剤組成物の製造
方法。
1 Natural rubber or synthetic rubber latex or resin emulsion (hereinafter abbreviated as latex etc.)
In an adhesive composition containing a filler, a thickener, and a heat-sensitive additive,
Added so that the viscosity at temperatures below ℃ is 10,000 to 40,000 cps as measured with a BM type viscometer at 6 rpm, and the viscosity increases to 100,000 cps or more at any desired temperature in the temperature range of 60 to 100 ℃ within 120 seconds. 1. A method for producing a carpet lining adhesive composition having good storage stability and blister resistance, which comprises blending a carpet lining adhesive composition.
JP8407580A 1980-06-23 1980-06-23 Preparation of adhesive composition for backing carpet Granted JPS5710665A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8407580A JPS5710665A (en) 1980-06-23 1980-06-23 Preparation of adhesive composition for backing carpet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8407580A JPS5710665A (en) 1980-06-23 1980-06-23 Preparation of adhesive composition for backing carpet

Publications (2)

Publication Number Publication Date
JPS5710665A JPS5710665A (en) 1982-01-20
JPS6255559B2 true JPS6255559B2 (en) 1987-11-20

Family

ID=13820356

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8407580A Granted JPS5710665A (en) 1980-06-23 1980-06-23 Preparation of adhesive composition for backing carpet

Country Status (1)

Country Link
JP (1) JPS5710665A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6426368U (en) * 1987-08-06 1989-02-14

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1333822C (en) * 1986-11-07 1995-01-03 Robert S. Beyersdorf Latex compositions useful as binders in composite board having dimensional stability and strength
JPH0778152B2 (en) * 1987-02-09 1995-08-23 武田薬品工業株式会社 Latex composition for carpet backing adhesive

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5295749A (en) * 1976-02-09 1977-08-11 Nippon Zeon Co Ltd Adhesive composition for backing carpet
JPS607068B2 (en) * 1978-02-22 1985-02-22 住友ノ−ガタック株式会社 Adhesive composition for carpet lining

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6426368U (en) * 1987-08-06 1989-02-14

Also Published As

Publication number Publication date
JPS5710665A (en) 1982-01-20

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