JPS5823867A - Remoistening hot-melt adhesive composition - Google Patents

Remoistening hot-melt adhesive composition

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Publication number
JPS5823867A
JPS5823867A JP12204281A JP12204281A JPS5823867A JP S5823867 A JPS5823867 A JP S5823867A JP 12204281 A JP12204281 A JP 12204281A JP 12204281 A JP12204281 A JP 12204281A JP S5823867 A JPS5823867 A JP S5823867A
Authority
JP
Japan
Prior art keywords
adhesive composition
paper
parts
degree
weight
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
JP12204281A
Other languages
Japanese (ja)
Inventor
Junichi Suenaga
末永 純一
Masao Washimi
鷲見 正雄
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.)
Unitika Chemical Co Ltd
Original Assignee
Unitika Chemical 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 Unitika Chemical Co Ltd filed Critical Unitika Chemical Co Ltd
Priority to JP12204281A priority Critical patent/JPS5823867A/en
Publication of JPS5823867A publication Critical patent/JPS5823867A/en
Pending legal-status Critical Current

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  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:The titled composition prepared by incorporating a specific PVA with a polyhydric alcoholic ester of boric acid and if necessary a plasticizer, having improved tackiness, adhesive force, blocking property, etc., and suitable for paper. CONSTITUTION:A composition prepared by incorporating 100pts.wt. PVA having a polymerization degree of 50-500, preferably 80-400, and a saponification degree of 40-80mol%, preferably 40-70mol%, maleic acid, with 0.5-50pts.wt. polyhydric alcoholic ester of boric acid, e.g. glycerol ester, and 0-200pts.wt. plasticizer, e.g. polyethylene glycol.

Description

【発明の詳細な説明】 本発明は、再湿性を有するホラtJIA/)接着剤組成
物に関する−ので島や、さらに評しくは水分散性を有し
主に紙7111m好適に用いられる再纒性ホツtメβ酬
襞曽*agt虞物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to adhesive compositions having rewetting properties, and more particularly to adhesive compositions having water dispersibility and being suitable for use mainly in paper 7111m. This is related to the possibility of getting a refund.

従来、封筒、テープ、切手、ヲペル、スIンプ。Traditionally, envelopes, tape, stamps, wopel, and stamps.

壁紙、ふすま紙には、可潜性でんぷん、S分ケシ化11
m’エルアρコー#(以下−夢ビエpア〃コー**Pマ
ムと略記する。)あるいはアク9に系樹脂のγμ力1塩
等力亀らなる再湿接着剤が用いられている。しかしなが
ら、これ等の再湿接着剤は熱溶融しないため、水溶液、
水分散液あるいは有機溶剤液として塗布する必要がある
ので、利用に際し乾燥工程が必要で生産性が悪く1重た
生麿工程中に互いにくっついたり、カールした9する欠
点があった◆ また、ホットメμトで―工される再湿ホラ)メ#)m着
剤として一9酢酸ビニルを酸ケン化して得た部分ケン化
PTA(米国特許第5.597,246号明細書)、完
全ケン化Pマムを再酢化して得た部分ケシ化Pマム(米
国特許第5,444,125号明細書)等特殊な製法で
慢た部分ケン化Pマム、親水性基(カμボン酸、ス〜傘
ン酸等)をもつモノマーで変性したPマ五等が搗案され
ているが、これ都の再製ホツ酬メA/)接着剤は製法が
複雑であったり得られた樹脂の熱安定性、w着性、プロ
ツ命ンダ性に間開があったりし、!!用化されていない
のが実情である。
Wallpaper and fusuma paper contain latent starch and S-poppy 11
A rewetting adhesive made of γμ force 1 salt is used for m'Elua ρ Co# (hereinafter abbreviated as ``YumebiepAco**Pmum'') or Aku9. However, these rewetting adhesives do not melt under heat, so
Since it needs to be applied as an aqueous dispersion or an organic solvent solution, it requires a drying process before use, resulting in poor productivity and problems such as sticking to each other or curling during the single rolling process. Partially saponified PTA (U.S. Pat. No. 5,597,246) obtained by acid saponifying vinyl mono9 acetate as an adhesive, completely saponified Partially saponified P-mum obtained by re-acetifying P-mum (U.S. Pat. No. 5,444,125), etc. Partially saponified P-mum obtained by a special manufacturing method, hydrophilic groups (carboxylic acid, sulphate, etc.) P-type adhesives modified with monomers containing phosphoric acid, etc.) have been proposed, but the manufacturing process for these adhesives is complicated and the resulting resin has poor thermal stability. There are gaps in sex, wetness, and pro-life sex. ! The reality is that it has not been put to practical use.

また、41会昭49−9611号会報には重合度200
−soo、ry化度70−80 q/&/優f)P T
 A ト可塑剤であるペンタニジスリトールとからなる
組成物が撮案されているが、この組成物は熱溶融粘度が
高かったり、熱安定性が悪い等の欠点があった。
In addition, in the 41st Society Bulletin No. 49-9611, the degree of polymerization is 200.
-soo, degree of oxidation 70-80 q/&/excellent f) P T
A composition comprising the plasticizer pentanidythritol has been proposed, but this composition has drawbacks such as high hot melt viscosity and poor thermal stability.

本発明者らは、かかる現状に鑞み、工業的l1cIl造
しやすいベースI9マーを用いて、速い再湿性優れたタ
ッタ性、低廖融粘度、良好な熱安定性。
The present inventors have taken advantage of this current situation and have developed a base I9mer that is easy to produce industrially and has fast rewetting properties, excellent tattering properties, low melting viscosity, and good thermal stability.

良好なブロッキング性を有し、さらに利用に際し作業性
の良い再湿ホットメルト接着剤組成物を提供することを
目的として鋭意研究した結果、特定の低重合度、低ケン
化度のPVAにホウ酸の◆価アμコーμエスデμ、必要
に応じて可塑剤をブレンドすることによって上記の目的
を達成しうろことを見い出し、零発WRC到適したもの
である。
As a result of intensive research aimed at providing a rewetting hot melt adhesive composition that has good blocking properties and is also easy to work with, we found that boric acid was added to PVA with a specific low degree of polymerization and low saponification. It was discovered that the above object could be achieved by blending the ◆ value of ACO and SDE, if necessary, with a plasticizer, and it was made suitable for zero-start WRC.

すなわち本発明は1重金度50〜500.ケン化度40
〜804N優のPVA100重量部、ホウ酸の多価アル
1コー〃エスデtv O,5〜50重量部及び可塑剤0
〜200重量部よりなる接着剤組成物である。
That is, the present invention has a hardness of 50 to 500. Saponification degree 40
-100 parts by weight of PVA of ~804N, 1 K of polyhydric alcohol of boric acid, 5-50 parts by weight of SDETV O, and 0 parts by weight of plasticizer.
-200 parts by weight of the adhesive composition.

表1に接着剤組成と物性の関係を示す0表1c示された
ように、低重合度、低ケン化度のPVA単独では再湿性
に乏しく、このPVAC可−剤のみを3会したものでは
再湿性は向上するものの!ツキネス、接着力は十分では
ない、これ等に*つ酸の多価アルコ−〜エステルを加え
ると再湿性。
Table 1 shows the relationship between adhesive composition and physical properties.As shown in Table 1c, PVA with a low degree of polymerization and low saponification alone has poor rewetting properties, and a mixture of only three PVAC plasticizers does not. Although rewetting performance improves! Toughness, adhesive strength is not sufficient, and when polyhydric alcohol ~ ester of acid is added to these, rewetting is possible.

タッキネス、接着力さらにブロッキング性までが向上す
る。PVA水溶液にホウ酸ないしその樵を加えれば増粘
し、タッキネスが向上する事はよく知られているが、ホ
ウ酸やホウ酸塩は熱溶融しないため、ホットメルト接着
剤にブレンドすることはできないので、タッキネスの向
上は望めない。
Improves tackiness, adhesion and even blocking properties. It is well known that adding boric acid or its salt to a PVA aqueous solution will increase its viscosity and improve its tackiness, but boric acid and borates do not melt with heat, so they cannot be blended into hot melt adhesives. Therefore, no improvement in tackiness can be expected.

本発明で使用するホウ酸の多価ア〜コーρエステルは常
温では粘稠な液体又は固体であり、熱溶融型のPVAに
溶融ブレンドされて若干の増粘を伴いながらタッキネス
向上の効果を発揮する。
The polyhydric alcohol-rho ester of boric acid used in the present invention is a viscous liquid or solid at room temperature, and when melt-blended with heat-melting PVA, it exhibits the effect of improving tackiness with slight thickening. do.

表1 接着剤組成と物性の関係 壷1上質紙C11I布量20 fedで論布したのち再
湿はり会わせ、ついで500ツ/dの荷重をかけて1分
間放置後、めくってその紙の破れ具合で判断した。
Table 1 Relationship between adhesive composition and physical properties Urn 1 High quality paper C11I Amount of cloth 20 After discussion with fed, rewet and rewet, then apply a load of 500 t/d and leave for 1 minute, then turn over and tear the paper. I judged it based on the situation.

壷2上質紙cm布量20 fedで塗布したのち木の欅
に強くまきつけ、ついでこれをはがして、そのはがれ具
合で判断した。
Jar 2 high-quality paper cm cloth amount 20 After applying with fed, wrap it tightly around a wooden zelkova, then peel it off and judge by the degree of peeling.

本発明に用いられるPVAは重合度50−500゜好ま
しくは80〜400.ケン化度40〜80モl&/g6
゜好ましくは40〜70七〜優であることが必要である
0重合度が50未満では接着力が不足し、500をこえ
る場合は溶融粘度が高くなるので適当でない、また、ケ
ン化度が40モル%未満では再湿性IC:L L < 
*  804ρ%をこえる場合は溶融温度。
The PVA used in the present invention has a polymerization degree of 50-500°, preferably 80-400°. Saponification degree 40-80mol&/g6
゜It is necessary that the degree of polymerization is preferably 40 to 70 to excellent. If the degree of polymerization is less than 50, the adhesive strength will be insufficient, and if it exceeds 500, the melt viscosity will be high, so it is not suitable. Also, if the degree of saponification is 40 If less than mol %, rewetting IC: L L <
*If it exceeds 804ρ%, it is the melting temperature.

粘度が高(なるので適当でない0本発明の特徴は・ホウ
酸の多価アμコーμエステμとPVAの相互作用による
タッキネス、接着力等の物性向上にあるのであるから、
使用するPVAはPVAとしての本質を失わない程度で
あれば他の七ツマ−で変性されたものでも差しつかえな
い、たとえばマレイン酸、アクリμ酸、メタアクリル酸
、クロトン酸及びこれ等の塩、ビニルピロリドン、オレ
フィン等で変性されたPVAも本発明において使用でき
る。
The viscosity is high (so it is not suitable).The feature of the present invention is that it improves physical properties such as tackiness and adhesive strength due to the interaction between polyvalent alcohol μ of boric acid and PVA.
The PVA used may be modified with other 7-mers as long as it does not lose its essence as PVA, such as maleic acid, acrylic acid, methacrylic acid, crotonic acid, and salts thereof. PVA modified with vinylpyrrolidone, olefins, etc. can also be used in the present invention.

本発明に使用するホウ酸の多価アルコ−〜エステルとし
ては、たとえば*つ酸のエチレング9コー、βエステ〜
、グリセリンエステル、ツルピトーρエステル、マンニ
トールエステルII カ、% ケ#) tLる。その中
でもグ、リセリンエステルが最も望ましイ、il加量e
iPTA100重量部Kitし0.5−50重量部、好
、ましくは5〜40重量部であることが必要である。0
.5重量部未満では接着力向上の効果は少なく、50重
量部をこえる場合は樹脂に腰がなくなるので適当でない
Examples of the polyalcohol to ester of boric acid used in the present invention include ethyl alcohol, β ester, and
, glycerin ester, tulpitot ρ ester, mannitol ester II, %, #) tLru. Among them, lycerin ester is the most desirable.
It is necessary that iPTA is 0.5 to 50 parts by weight, preferably 5 to 40 parts by weight, based on 100 parts by weight of iPTA. 0
.. If it is less than 5 parts by weight, the effect of improving adhesive strength will be small, and if it exceeds 50 parts by weight, the resin will lose its elasticity, which is not suitable.

本発明に用いる可塑剤としては1通常PVAに用いられ
る可塑剤ならばどのようなものでも用いられるが、好ま
しい具体例としてはエチレングリコ−μ、トリメチレン
グリコール、テトツメチレングリコール、ペンタメチレ
ングリコ−〜、ヘキサメチレングリコー〜、グロビレン
グリスー〜。
As the plasticizer used in the present invention, any plasticizer commonly used for PVA can be used, but specific examples include ethylene glycol-μ, trimethylene glycol, tetotumethylene glycol, pentamethylene glycol, etc. , hexamethylene glycol ~, globylene glycol ~.

グリセリン、2.S−ブタンジオ−〜、1.5−ブタン
ジオール、シエチVングリコール、ドリエチ、レンダ9
コーsr、19エチレングリ−コール、エチレン尿素、
尿素、ツルピトー〜、アンニドーρ等があげられる。こ
れらのなかでも再湿性、可暖性。
Glycerin, 2. S-butanedio-, 1,5-butanediol, siethi V glycol, doriethi, Renda 9
Coat sr, 19 ethylene glycol, ethylene urea,
Examples include urea, turpitou, annido rho, etc. Among these, rewetting and warmability.

耐熱性の面からエチレングリコール、グリセリン。Ethylene glycol and glycerin for their heat resistance.

分子量200〜2000のlリエチレングリコー〜がと
くに望ましい、かかる可畷剤の添加量はPvム100重
量部に対し0〜200部用いる。’200部をこえる場
合は接着剤組成物の溶融粘度が低くなるので塗布は春易
になるものの接着力が低下し、ブーツキング性も悪くな
る傾崗があるため好ましくない。
Particularly preferred is l-lyethylene glycol having a molecular weight of 200 to 2,000.The amount of such fusing agent added is 0 to 200 parts per 100 parts by weight of Pvum. If it exceeds 200 parts, the melt viscosity of the adhesive composition decreases, making it easier to apply, but it is not preferable because the adhesive strength decreases and there is a tendency to deteriorate boot kingability.

本発明の接着剤組成物は、たとえば上記の低重合度、低
ケン化度のPTAICホウ酸の◆価アルコーμを添加し
、必要に応じてさらに可−剤を加えよくブレンドしたの
ち180〜200 cに加熱して各成分を溶融混練する
ことにより調製することができる。このようにして調製
された溶融物はそのままコーター等で紙に塗布すること
もできるし、またいったん溶融物を押し出し、チップ状
にしたのち使用時に再溶融しコーター等で紙#C論塗布
ることもできる。この場合9本発明の接着剤組成物の溶
融粘度が500〜5000 o、p、a、程度であれば
、従来のノズルタイプあるいはローラータイプのコータ
ーが使用できるのでとくに好都合である。
The adhesive composition of the present invention can be prepared by adding, for example, the ◆hydric alcohol μ of PTAIC boric acid with a low degree of polymerization and low saponification, and adding a plasticizing agent as necessary and thoroughly blending the adhesive composition. It can be prepared by melting and kneading each component by heating to c. The melt prepared in this way can be directly applied to paper using a coater, etc., or it can be extruded and made into chips, then remelted before use and applied to paper using a coater, etc. You can also do it. In this case, it is particularly convenient if the adhesive composition of the present invention has a melt viscosity of about 500 to 5000 o, p, a, since a conventional nozzle type or roller type coater can be used.

本発明の再湿ホットメルト接着剤組成物には。The rewet hot melt adhesive composition of the present invention includes:

目的とする再湿性、接着性な失うことがない範囲で他の
添加剤、たとえばロジン樹脂、エチレン−酢ビ樹脂、タ
ッキファイヤ−,滑剤ワックス、鎖料、染料、香料、抗
酸化剤、熱安定剤を含有させることができる。
Other additives to the extent that the desired rewetting and adhesion properties are not lost, such as rosin resin, ethylene-vinyl acetate resin, tackifier, lubricant wax, chain additive, dye, fragrance, antioxidant, heat stabilizer. It is possible to contain an agent.

本発明の接着剤組成物は、再湿接着剤に適しており、た
とえば封筒、デーデ、切手、収入印紙。
The adhesive composition of the invention is suitable for rewetting adhesives, such as envelopes, stamps, stamps, revenue stamps.

フペμ、スタンプ、壁紙に用いられる。また9本発明の
接着剤組成物はホットメルト性をも有しているので、た
とえば感熱紙、ヒー) V −A/、剤に用いることも
できる。ま、た9本−明の接着剤組成物は水溶性ないし
水分散性であるので、たと、えばこれを適用した故紙を
回収する際にフィμターの日づ重り、ローフ−の汚れ、
製品のピンホールや斑点の発生等のトラプ〜がないとい
う利点を有する。
Used for Fupé μ, stamps, and wallpaper. Furthermore, since the adhesive composition of the present invention also has hot-melt properties, it can also be used for, for example, thermal paper, heat-sensitive paper, and adhesives. Furthermore, since the adhesive composition of Ta9motomei is water-soluble or water-dispersible, for example, when collecting waste paper to which it has been applied, it may cause stains on the filter, stains on the loaf, etc.
It has the advantage that there are no traps such as pinholes or spots on the product.

以下実施例をあげて本発明をさらに具体的に説明する。The present invention will be explained in more detail below by giving examples.

なお9例中の「部」を「重量部」を意味する。Note that "parts" in the nine examples mean "parts by weight."

実施例1 重合度120.ケン化度554μ%のPマム100部に
ホウ酸のグ―セリンエステs、’so部を加え。
Example 1 Degree of polymerization 120. To 100 parts of P-mum with a degree of saponification of 554 μ%, add 1 part of boric acid, Gucerine Esthes.'so.

180 Cで溶融ブレンドした。このブレンド物は18
0Cで4100 o、p、s、の*a粘度を示した。こ
のようにして得た接着剤組成物を溶融してローラーゴー
声−で坪量550 f/dのフイナー1c10f/ml
cなるよう塗布した。このフイナーを同質のライナーc
@着爾積が15 X 15−に重ね、再湿して接着し、
  0.25 kl/−で10秒間圧着した。得られた
接着片の引張り剪断力を測定したところ18.7 #/
dであった。また、岡じ接着面積で重ねた紙片を再湿せ
ずにアイーンで150CN:加熱し、接着圧2〜5#/
−で10秒間圧着したのち、同様にして引張り剪断力を
測定したところ18.Ojl、4であった。
Melt blended at 180C. This blend is 18
It exhibited an *a viscosity of 4100 o, p, s, at 0C. The adhesive composition thus obtained was melted and rolled to give a filler 1c10f/ml with a basis weight of 550 f/d.
It was applied so that it became c. This filler is made of a homogeneous liner c
@Layered 15 x 15-, re-moistened and glued,
Pressure was applied for 10 seconds at 0.25 kl/-. When the tensile shear force of the obtained adhesive piece was measured, it was 18.7 #/
It was d. In addition, without re-wetting the stacked paper pieces with the same adhesive area, heat the sheets with an iron for 150CN and apply an adhesive pressure of 2 to 5 #/
- After crimping for 10 seconds, the tensile shear force was measured in the same way. It was Ojl, 4.

実施例2 重合度140.ケン化度60モル優のPvム100部、
ホウ酸のグリセリンエステpv(WH品名GB−90東
邦化学工業株式会社)5部及びグ9−9ン80部を18
0℃で溶融ブレンドして、160℃の溶融粘度が150
0 o、p、s、の接着剤組成物を得た。
Example 2 Degree of polymerization 140. 100 parts of Pvmu with a saponification degree of 60 moles,
5 parts of glycerine ester pv of boric acid (WH product name GB-90 Toho Chemical Industry Co., Ltd.) and 80 parts of G9-9 to 18
Melt blend at 0℃, melt viscosity at 160℃ is 150
An adhesive composition of 0 o, p, s was obtained.

このものをローフ−コーターで厚さ0.08 mの上質
紙に坪量159/dになるように塗布してのり引き紙を
作成した。得られたのり引き紙を水にぬらして別の同質
の上質紙に貼り合わせたのち、5分後に剥がしたところ
紙が破れる接着性を示した。また、上記ののり引き紙を
1000枚重ねて1力月放置したがカールやブロッキン
グの問題はなかった。
This product was coated on a 0.08 m thick high quality paper using a loaf coater to give a basis weight of 159/d to prepare a pasted paper. The resulting glued paper was wetted with water and bonded to another high-quality paper of the same quality, and when peeled off after 5 minutes, the paper showed adhesiveness that caused it to tear. Furthermore, when 1,000 sheets of the above glued paper were stacked and left for one month, there were no problems with curling or blocking.

また、上記の接着剤組成物は常温の水に白濁溶解するも
のであった。
Further, the above adhesive composition dissolved in cloudy water at room temperature.

実施例S 重合度80.ケン化度70屹p%のPマム100部、!
J施何例1用いたのと同じホウ酸のグリセ曽ンエステ〜
10部及びメジエチレングリコ−〜(分子量600 )
 100部を溶融プレンrして、160℃の溶融粘度が
1000 o、p、s、の接着剤組成物を得たこれを一
一フー=−!−で厚さO,Oa−の上質紙に坪量20 
#/dとなるように塗布してのり引か紙を作成した。こ
ののり引き紙を再湿して他の別の同質の上質紙にはり舎
すせたのち、10分後に剥がしたところ紙層が破れる接
着性を示した。また。
Example S Degree of polymerization 80. 100 copies of P-Mum with a saponification degree of 70 p%!
The same boric acid griseon esthetics used in J Example 1.
10 parts and mediethylene glycol (molecular weight 600)
100 parts were melt-prened to obtain an adhesive composition with a melt viscosity of 1000 o, p, s at 160°C. - thickness O, Oa- high quality paper with basis weight 20
A glued paper was prepared by applying the mixture to a ratio of #/d. This pasted paper was re-moistened and pasted on another high-quality paper of the same quality, and when peeled off after 10 minutes, the paper layer showed adhesiveness that caused it to tear. Also.

再湿甘ずC,の9を塗布した面に別の同質の上質紙を重
ね舎わ昔120cのアイロンで10秒間加熱したのも1
5秒間放冷して剥がしたところ紙層が破れる接着性を示
した。また、上記ののり引き紙を1000枚重ねて1力
月放置したがブロッキングやカールの問題は!IIII
なかった。また、上記の接着剤編成物は常温の水に溶解
するものであり、故紙回収になんら支障のないものであ
った。
I layered another high-quality paper of the same quality on the surface coated with re-wetting Amazu C.9 and heated it with a 120c iron for 10 seconds.
When it was allowed to cool for 5 seconds and then peeled off, it showed adhesiveness that caused the paper layer to tear. Also, I stacked 1000 sheets of the above glue paper and left it for a month, but there were no problems with blocking or curling! III
There wasn't. In addition, the above-mentioned adhesive knitted material was soluble in water at room temperature, and there was no problem in recovering waste paper.

実施例4 重合度400.ケン化度55嫌ル%の271100部、
傘?晴のエチVングリコー〃エステμm、0部ソμピト
ーμ40部1びエチレングリコ−μ40部を溶融プレン
Yして、160℃の溶融粘度が5000o、p、s、の
接着剤組成物を得た。このものな−−ラーコ−p−で厚
さ0.08 gの上質紙に坪量25 f/dになるよう
に塗布してのり引き紙を作成した。得られたこののり引
き紙について実施例3と同様にして再湿接着性、ヒート
V−〜性を−ベたが両者と4h良好であった。
Example 4 Degree of polymerization 400. 271,100 parts with a saponification degree of 55%,
umbrella? Hareno Echi V-Glyco Este μm, 0 parts Soμ Pito μ 40 parts 1 and Ethylene Glyco-μ 40 parts were melt-plane Y to obtain an adhesive composition with a melt viscosity of 5000 o, p, s at 160°C. . This paste was applied to a 0.08 g thick high-quality paper using Larco-P to give a basis weight of 25 f/d to make glued paper. The obtained pasted paper was tested for rewet adhesion and heat V-ability in the same manner as in Example 3, and both were good for 4 hours.

また、上記ののり引き紙を1000枚重ねて1力月放置
したが、ブロッキングやカールの問題は句会なかった。
Also, I stacked 1,000 sheets of the above glue paper and left it for a month, but there were no problems with blocking or curling.

また、上記の接着剤組成物は常温の水に白濁分散するも
のであり、故紙回収の際なんら支障なtたさないもので
あった。
Furthermore, the above adhesive composition was dispersible in cloudy water at room temperature and did not pose any problem when recovering waste paper.

特許出願人  ユニチカケミカル株式会社代珊人 児玉
嫌=
Patent applicant: Unitika Chemical Co., Ltd. Yosanto Kodama Haku =

Claims (1)

【特許請求の範囲】[Claims] (1)重合度5O−5on、ケン化度40−60モ〜優
の4!ビニルアルコ−*100重量部、ホウ酸の◆価ア
ル:l−ルエステ#0.S−ルO重量allび可−剤0
−200重量部よりなる接着剤組成物。 (坤傘9酸の◆偏アμゴーμエスデlkl#!傘つ酸の
ダーセ豐ンエステルである特許請求の一一第1項記載の
接着剤組成物。
(1) Degree of polymerization: 5O-5on, degree of saponification: 40-60% to excellent 4! Vinyl alcohol *100 parts by weight, ◆valent alkyl of boric acid: L-Este #0. S-ru O weight all and softener 0
- an adhesive composition consisting of 200 parts by weight. (The adhesive composition according to claim 11, wherein the adhesive composition is a ◆polarized μgoμesdelkl#! diacetate ester of paraglycic acid.
JP12204281A 1981-08-04 1981-08-04 Remoistening hot-melt adhesive composition Pending JPS5823867A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12204281A JPS5823867A (en) 1981-08-04 1981-08-04 Remoistening hot-melt adhesive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12204281A JPS5823867A (en) 1981-08-04 1981-08-04 Remoistening hot-melt adhesive composition

Publications (1)

Publication Number Publication Date
JPS5823867A true JPS5823867A (en) 1983-02-12

Family

ID=14826160

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12204281A Pending JPS5823867A (en) 1981-08-04 1981-08-04 Remoistening hot-melt adhesive composition

Country Status (1)

Country Link
JP (1) JPS5823867A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6048962A (en) * 1983-08-26 1985-03-16 Chisso Corp Preparation of sulfamic acid guanidine
JPS60106869A (en) * 1983-11-14 1985-06-12 Mitsubishi Rayon Co Ltd Paste for protective sheet and surface-protected synthetic resin molding using the same
JPS60106870A (en) * 1983-11-14 1985-06-12 Mitsubishi Rayon Co Ltd Paste for protective sheet and surface-protected synthetic resin molding using the same
EP1310532A1 (en) * 2001-11-09 2003-05-14 Xerox Corporation Phase change inks containing borate esters
CN103724899A (en) * 2013-12-30 2014-04-16 浙江七色鹿色母粒有限公司 Thermal plasticizing polyvinyl alcohol modified material

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6048962A (en) * 1983-08-26 1985-03-16 Chisso Corp Preparation of sulfamic acid guanidine
JPH038335B2 (en) * 1983-08-26 1991-02-05 Chisso Corp
JPS60106869A (en) * 1983-11-14 1985-06-12 Mitsubishi Rayon Co Ltd Paste for protective sheet and surface-protected synthetic resin molding using the same
JPS60106870A (en) * 1983-11-14 1985-06-12 Mitsubishi Rayon Co Ltd Paste for protective sheet and surface-protected synthetic resin molding using the same
JPH0430429B2 (en) * 1983-11-14 1992-05-21
JPH0437111B2 (en) * 1983-11-14 1992-06-18 Mitsubishi Rayon Co
EP1310532A1 (en) * 2001-11-09 2003-05-14 Xerox Corporation Phase change inks containing borate esters
CN103724899A (en) * 2013-12-30 2014-04-16 浙江七色鹿色母粒有限公司 Thermal plasticizing polyvinyl alcohol modified material

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