JPH07331202A - Paste-making method for starch adhesive for corrugated board - Google Patents
Paste-making method for starch adhesive for corrugated boardInfo
- Publication number
- JPH07331202A JPH07331202A JP6155327A JP15532794A JPH07331202A JP H07331202 A JPH07331202 A JP H07331202A JP 6155327 A JP6155327 A JP 6155327A JP 15532794 A JP15532794 A JP 15532794A JP H07331202 A JPH07331202 A JP H07331202A
- Authority
- JP
- Japan
- Prior art keywords
- starch
- adhesive
- paste
- boric acid
- swelling
- 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
Links
Landscapes
- Making Paper Articles (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は段ボールの製造に用いら
れる澱粉系接着剤の製糊方法に関する。さらに詳しく
は、本発明はノーキャリア方式の製糊において機械的剪
断力を伴う強撹拌手段を用いたことを特徴とする段ボー
ル用澱粉接着剤の製糊方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for making a starch-based adhesive paste used for producing corrugated board. More specifically, the present invention relates to a paste making method for a starch adhesive for corrugated board, which is characterized in that a strong stirring means accompanied by mechanical shearing force is used in the paste making of no carrier method.
【0002】[0002]
【従来の技術】従来、一般に、段ボールの製造に使用さ
れる澱粉接着剤は、キャリア部と呼ばれるアルカリ糊化
した澱粉糊液と、メイン部と呼ばれる未糊化澱粉の懸濁
液との混合物からなっており、この接着剤は、ステイン
ホール方式と呼ばれる製糊方法で製造されている。この
製糊方法ではメイン部とキャリア部を別々に調製したう
え、両者を混合する手法が採られるため、製法が煩雑で
品質的にも接着剤自体の粘度がバラツキ易く、安定した
接着剤を得るのに熟練を要するという難点がある。2. Description of the Related Art Conventionally, a starch adhesive used in the manufacture of corrugated board is generally composed of a mixture of an alkali gelatinized starch paste solution called a carrier part and a suspension of ungelatinized starch called a main part. This adhesive is manufactured by a sizing method called a stain hole method. In this pasting method, the main part and the carrier part are prepared separately, and the method of mixing both is adopted, so the manufacturing process is complicated, and the viscosity of the adhesive itself tends to vary, and a stable adhesive is obtained. There is a drawback that it requires skill.
【0003】このような煩雑な操作を解消し安定した品
質の接着剤を得るためにノーキャリア方式と呼ばれる製
糊方法が提案されている。ノーキャリア方式は、アルカ
リにより全体の澱粉を部分膨潤状態にして適度な粘性を
付与する方法であって、ステインホール方式と比較して
製糊は簡単で、機械的剪断や温度変化に対しての粘度安
定性においてもステインホール方式より優れているが、
保水性や流動性に難点があり、初期接着性や高速貼合適
性も十分とはいい難い。In order to eliminate such complicated operations and obtain an adhesive having stable quality, a gluing method called a no carrier method has been proposed. The no-carrier method is a method in which the entire starch is partially swollen with an alkali to give it an appropriate viscosity.Comparing with the stain-hole method, the paste making is easier and it is more resistant to mechanical shearing and temperature change. It is also superior to the stain hole method in viscosity stability,
There are problems in water retention and fluidity, and initial adhesiveness and suitability for high-speed laminating are not enough.
【0004】ノーキャリア方式の改良法として、冷水可
溶性のアルファー化澱粉を未加工の澱粉と予め混合して
おき、これに、撹拌下にアルカリを加えてアルファー化
澱粉を溶解すると共に未加工の澱粉を部分膨潤させる方
法が知られている。この改良方法により得られる澱粉は
粘度安定性と流動性のバランスがとれている。また、初
期接着性も通常のノーキャリア方式に比べてかなり改良
されている。しかしながら、アルファー化澱粉の溶解性
によっては粘度安定性が悪化したり、澱粉溶解時にママ
コが生じやすいなどの問題がある。As an improved method of the no-carrier method, cold water-soluble pregelatinized starch is premixed with raw starch, and an alkali is added to this to dissolve the pregelatinized starch while the raw starch is dissolved. A method of partially swelling is known. The starch obtained by this improvement method has a good balance of viscosity stability and fluidity. Also, the initial adhesiveness is considerably improved as compared with the normal no-carrier method. However, depending on the solubility of the pregelatinized starch, there are problems such that the viscosity stability is deteriorated, and mamako tends to occur when the starch is dissolved.
【0005】これらノーキャリア方式の問題点の解決を
目的として、アルファー化澱粉の改良された製造方法が
提案されている(例えば、特開平3−12470、特開
平3−17175、特開平5−155901など)。し
かしながら、これらの改良方法においてもアルファー化
澱粉の粒度の設定や添加剤(硼酸塩、硫酸塩、尿素、糖
類など)との混合が必要になる場合があり、澱粉の水へ
の溶解に時間をかけ充分注意して作業を行ってもママコ
の発生を完全には抑えられない場合が多い。For the purpose of solving these problems of the no-carrier method, an improved method for producing pregelatinized starch has been proposed (for example, JP-A-3-12470, JP-A-3-17175, JP-A-5-155901). Such). However, even in these improved methods, it may be necessary to set the particle size of pregelatinized starch and mix it with additives (borate, sulfate, urea, saccharide, etc.), and it takes time to dissolve starch in water. In many cases, it is not possible to completely suppress the occurrence of mamako even if the work is done with great care.
【0006】上述のように、従来の段ボール用接着剤
は、製糊の煩雑さや澱粉溶解時の問題点を解消し、高速
貼合適性を高めるため改良を試みたものであるが、これ
ら全てを満足させるに至っていない。[0006] As described above, the conventional corrugated board adhesives have been attempted to be improved in order to solve the complication of the paste making process and the problems when the starch is dissolved, and to enhance the suitability for high-speed bonding. Not yet satisfied.
【0007】[0007]
【発明が解決しようとする課題】本発明の目的は、ノー
キャリア方式による従来の段ボール接着剤の難点である
製糊の煩雑さや澱粉溶解時の問題点を解消し、更に接着
剤の流動性や初期接着性が向上され、高速貼合にも適し
た段ボール用接着剤を提供することにある。SUMMARY OF THE INVENTION The object of the present invention is to solve the problems associated with the conventional corrugated board adhesives of the no-carrier system, such as the complexity of the paste-making paste and the problem of starch dissolution, and to improve the fluidity of the adhesives. An object of the present invention is to provide an adhesive for corrugated board which has improved initial adhesiveness and is also suitable for high-speed bonding.
【0008】[0008]
【課題を解決するための手段】本発明者らは、上記課題
を解決するために種々検討した結果、ノーキャリア方式
の段ボール用接着剤の製造方法において、高い機械的剪
断力を付与する強撹拌製糊手段を組み合わせ採用するこ
とによって上記課題を解決できることを見いだし、本発
明を完成するに至った。As a result of various studies to solve the above problems, the present inventors have found that in a method for producing a carrier-free adhesive for corrugated board, strong stirring that imparts high mechanical shearing force. It has been found that the above-mentioned problems can be solved by adopting a combination of sizing means, and the present invention has been completed.
【0009】すなわち、本発明は、澱粉の水性懸濁液に
過剰量のアルカリを加えて全体の澱粉を部分膨潤状態に
し、次いで硼酸または硼酸と硼砂を加えることによって
膨潤を停止して適度な粘度を有する段ボール用接着剤を
得る工程を含むノーキャリア方式による製糊方法におい
て、500m/min以上の周速を有する強力撹拌手段
で剪断をかけながら上記部分膨潤化および膨潤停止を行
うことを特徴とする段ボール用澱粉接着剤の製糊方法で
ある。That is, according to the present invention, an excessive amount of alkali is added to an aqueous suspension of starch to partially swell the whole starch, and then boric acid or boric acid and borax are added to stop the swelling and to give an appropriate viscosity. In a paste making method by a no-carrier method including a step of obtaining an adhesive for corrugated board, the partial swelling and the swelling stop are performed while shearing with a powerful stirring means having a peripheral speed of 500 m / min or more. This is a method for making a starch adhesive for corrugated board.
【0010】以下、本発明の段ボール用澱粉接着剤の製
糊方法を詳細に説明する。本発明において使用する澱粉
は、通常のノーキャリア方式で使用する澱粉で良く、特
に限定されないが、未加工のコーンスターチ(ハイアミ
ロースコーンスターチやワキシーコーンスターチも含
む)、馬鈴薯、タピオカ、小麦、甘藷等の澱粉もしくは
これらを組み合わせたものが一般に用いられる。The method for making the starch adhesive for corrugated board of the present invention will be described in detail below. The starch used in the present invention may be a starch used in a normal no-carrier method, and is not particularly limited, but raw corn starch (including high amylose corn starch and waxy corn starch), potato, tapioca, wheat, starch such as sweet potato Alternatively, a combination of these is generally used.
【0011】本発明の効果をより大きくするためには、
アルカリアミログラフにおける糊化開始温度が上記の主
たる未加工澱粉より5℃以上、より好ましくは10℃以
上低い澱粉(以下、従たる澱粉という)を未加工澱粉に
組み合わせて用いる。この従たる澱粉としては、常法に
従ってエーテル化、エステル化、グラフト化またはこれ
らの組み合わせにより糊化開始温度を下げた加工澱粉
か、または主たる澱粉より糊化開始温度が5℃以上低い
未加工の澱粉を使用できる。ここで、アルカリアミログ
ラフとは澱粉30gを450gの水性懸濁液とし、これ
に4.9重量%のカセイソーダ50mlを加えた場合の
アミログラフであって、100BU通過時の温度を糊化
開始温度とする。また、これらの従たる澱粉は酸化、酸
処理、デキストリン化などの低粘度化処理が施されてい
ても良い。In order to enhance the effect of the present invention,
A starch (hereinafter referred to as a subordinate starch) having a gelatinization initiation temperature in an alkaline amylograph lower than that of the above-mentioned main raw starch by 5 ° C. or more, more preferably by 10 ° C. or more is used in combination with the raw starch. The subordinate starch may be a processed starch whose gelatinization start temperature is lowered by etherification, esterification, grafting or a combination thereof according to a conventional method, or an unprocessed starch whose gelatinization start temperature is 5 ° C. or more lower than that of the main starch. Starch can be used. Here, the alkali amylograph is an amylograph in which 30 g of starch is made into an aqueous suspension of 450 g and 50 ml of 4.9 wt% caustic soda is added, and the temperature at the time of passing 100 BU is the gelatinization start temperature. To do. Further, these subordinate starches may be subjected to a treatment for lowering viscosity such as oxidation, acid treatment, and dextrinization.
【0012】これらの澱粉の配合比率および水と澱粉組
成物との倍水比(重量基準での澱粉に対する水の倍数)
は、初期接着力、常態接着力や接着剤の流動性を考慮し
て適宜設定されるべきである。主たる澱粉に対する従た
る澱粉の配合比率(重量比)は1〜30重量%、より好
ましくは3〜20重量%の範囲とする。また、倍水比は
2〜4の範囲が好ましい。Mixing ratio of these starches and double water ratio of water to starch composition (multiple of water to starch on a weight basis)
Should be appropriately set in consideration of the initial adhesive strength, the normal adhesive strength, and the fluidity of the adhesive. The blending ratio (weight ratio) of the subordinate starch to the main starch is 1 to 30% by weight, more preferably 3 to 20% by weight. The double water ratio is preferably in the range of 2 to 4.
【0013】本発明の製糊方法においては強撹拌手段に
より剪断力をかけながら製糊を行う。強撹拌手段として
は、強い機械的剪断力を付与することができるものであ
ればよく、例えば、ディスパーサータイプ、ミキサータ
イプ、ホモジナイザータイプ、ミルタイプなどの撹拌機
が挙げられるが、懸濁液全体を常に流動状態に保持でき
るタイプの撹拌機が用いられる。また、懸濁液全体を流
動させるために低速の撹拌機を補助として併用してもよ
い。In the pasting method of the present invention, pasting is performed while applying a shearing force with a strong stirring means. The strong stirring means may be any one capable of imparting a strong mechanical shearing force, and examples thereof include a disperser type, a mixer type, a homogenizer type, and a mill type stirrer. A stirrer of the type that can always maintain the fluid state is used. In addition, a low-speed stirrer may be used as an auxiliary in order to fluidize the entire suspension.
【0014】強撹拌手段は、撹拌手段のタイプや用いる
澱粉のタイプにもよるが、500m/min以上の周速
にて用いる。撹拌手段の周速が500m/min未満で
は通常の低撹拌装置を使用した場合との効果の違いが顕
著でなく、本発明の目的が達成されない。また、周速の
上限は格別限定されるものではないが、撹拌装置の剪断
による発熱によって自ら制限されるため、一般に、周速
の上限は3,000〜4,000m/min程度であ
る。The strong stirring means is used at a peripheral speed of 500 m / min or more, depending on the type of stirring means and the type of starch used. When the peripheral speed of the stirring means is less than 500 m / min, the difference in effect from the case of using a normal low stirring device is not remarkable, and the object of the present invention is not achieved. The upper limit of the peripheral speed is not particularly limited, but is generally limited by the heat generated by the shearing of the stirring device, and therefore the upper limit of the peripheral speed is generally about 3,000 to 4,000 m / min.
【0015】本発明の製糊方法において、澱粉の水性懸
濁液に過剰量のアルカリを加えて全体の澱粉を部分膨潤
状態にし、次いで硼酸または硼酸と硼砂を加えることに
よって膨潤を停止して適度な粘度を有する澱粉接着剤を
得る工程は、強い剪断力を付与することを除けば、従来
のノーキャリア方式による製糊方法におけると同様に行
うことができる。In the paste making method of the present invention, an excessive amount of alkali is added to an aqueous suspension of starch to partially swell the whole starch, and then boric acid or boric acid and borax are added to stop the swelling to an appropriate degree. The step of obtaining a starch adhesive having a sufficient viscosity can be performed in the same manner as in the pasting method by the conventional no carrier method, except that a strong shearing force is applied.
【0016】澱粉の膨潤化剤としてのアルカリとしては
苛性ソーダなどのアルカリ金属水酸化物を使用し、また
澱粉の膨潤停止剤および接着強度補助剤として硼酸を添
加する。また、必要に応じて、さらに硼砂を添加するこ
ともある。これらの添加量は製糊時間、接着剤の粘度、
接着剤自体の糊化温度、接着強度などを勘案して設定さ
れるものであるが、アルカリの添加量は対澱粉2〜5重
量%、硼酸の添加量は対澱粉0.5〜3重量%、また硼
砂の添加量は対澱粉1〜3重量%の範囲が好ましい。ま
た、製糊時における懸濁液の温度は製糊時間や接着剤の
糊化温度を考えて決めるが20〜45℃の範囲が好まし
い。また、必要に応じて、接着剤に耐水化剤、消泡剤、
防腐剤などを添加してもよい。An alkali metal hydroxide such as caustic soda is used as an alkali as a starch swelling agent, and boric acid is added as a starch swelling stopper and an adhesive strength aid. In addition, borax may be further added if necessary. The amount of these added is the glue making time, the viscosity of the adhesive,
It is set in consideration of the gelatinization temperature and the adhesive strength of the adhesive itself, but the amount of alkali added is 2 to 5% by weight of starch, and the amount of boric acid added is 0.5 to 3% by weight of starch. The amount of borax added is preferably in the range of 1 to 3% by weight of starch. Further, the temperature of the suspension during gluing is determined in consideration of the gluing time and the gelatinization temperature of the adhesive, but is preferably in the range of 20 to 45 ° C. In addition, if necessary, the adhesive may be water resistant, defoaming agent,
Preservatives and the like may be added.
【0017】[0017]
【発明の効果】本発明のノーキャリア方式による段ボー
ル用澱粉接着剤の製法は従来の方法に比べて以下のよう
な利点がある。 (イ)ママコが生成せず澱粉のタンクへの溶解が非常に
簡単になる。 (ロ)強撹拌によりアルカリを高濃度でより短時間に添
加できる。 (ハ)強撹拌(強剪断)を施すため、アルカリと熱によ
り膨潤した澱粉の分散が進み、流動性が改善される。特
にこの効果は糊化開始温度の低い従たる澱粉において顕
著であり、分散の進んだ澱粉がステインホール方式のキ
ャリア部の働きをする。The method for producing a starch adhesive for corrugated board using the carrierless method of the present invention has the following advantages over the conventional methods. (B) Mamako is not generated, and the dissolution of starch in the tank becomes very easy. (B) With strong stirring, the alkali can be added at a high concentration in a shorter time. (C) Since strong stirring (strong shearing) is applied, the starch swollen by alkali and heat is dispersed, and the fluidity is improved. In particular, this effect is remarkable in the subordinate starch having a low gelatinization starting temperature, and the starch having advanced dispersion functions as a carrier portion of the stain hole system.
【0018】(ニ)従たる澱粉の分散が進んでいるため
に段ボール原紙との絡みが良くなり、初期接着性が向上
する。 (ホ)従たる澱粉を適切に選ぶことにより従来のノーキ
ャリア方式では困難であった低倍水比での製糊が可能に
なる。 (ヘ)この段ボール用接着剤を高速貼合に用いれば、接
着不良の発生も少なく安定な段ボールの製造が可能とな
る。(D) Since the secondary starch is further dispersed, the entanglement with the cardboard base paper is improved, and the initial adhesiveness is improved. (E) By appropriately selecting the subordinate starch, it becomes possible to make a paste with a low water doubling ratio, which was difficult with the conventional no-carrier method. (F) If this adhesive for corrugated board is used for high-speed bonding, stable corrugated board can be manufactured with less occurrence of adhesion failure.
【0019】[0019]
【実施例】以下に実施例をもって本発明の効果を説明す
るが、前述の説明及び実施例で使われている特性は以下
の方法によって測定し、評価した。 (1)流動性 接着剤の流動特性は、接着剤をビーカーから流出させた
時の流れ方で判断し、◎ 優秀(ロングな接着剤、接着
剤全体の流動性がよい)、○ 良好(かなりロングな接
着剤)、△ 普通、× 不良(ショートな接着剤、ボソ
ボソな接着剤)と表示する。EXAMPLES The effects of the present invention will be described below with reference to examples. The characteristics used in the above description and examples were measured and evaluated by the following methods. (1) Flowability The flowability of the adhesive is judged by the flow of the adhesive when it flows out of the beaker. Excellent (long adhesive, good flowability of the whole adhesive), good (very good) Long adhesive), △ Normal, × Poor (short adhesive, sloppy adhesive).
【0020】(2)初期接着力 ガラス板上に製糊後39℃、60分保存した後の接着剤
糊液を一定量塗布し、A段片段ボール(K220×12
5)の段頂に糊付けする。これを直ちに110℃に加熱
したライナー(K220、12×13cm)に貼合し、
ピンテスターとオートレコーダーとを組み合わせた装置
で5秒間の加圧貼合後直ちに剥離した時の強度(応力)
を測定する。 (3)常態接着力 ガラス板上に製糊後39℃、60分保存した後の接着剤
糊液を一定量塗布し、A段(K280×180)の段頂
部に糊付けする。これを、120℃に加熱したライナー
(K280、5×8cm)に乗せ、5秒間加圧貼合して
サンプルを得る。これを、20℃、65RH%の条件下
で3日間調湿した後、JISに基づいて測定する。(2) Initial adhesive strength A predetermined amount of adhesive glue liquid after being glued on a glass plate and stored at 39 ° C. for 60 minutes is applied, and corrugated cardboard of A-stage (K220 × 12)
Glue to the top of 5). Immediately attach it to a liner (K220, 12 × 13 cm) heated to 110 ° C.,
Strength (stress) when immediately peeled after pressure bonding for 5 seconds with a device that combines a pin tester and an auto recorder
To measure. (3) Normal-state adhesive strength A predetermined amount of an adhesive paste solution, which has been glued on a glass plate and stored at 39 ° C. for 60 minutes, is applied and glued to the top of the A-tier (K280 × 180). This is placed on a liner (K280, 5 × 8 cm) heated to 120 ° C. and pressure-bonded for 5 seconds to obtain a sample. This is conditioned under the conditions of 20 ° C. and 65 RH% for 3 days, and then measured according to JIS.
【0021】実施例1 強剪断力を有するコーレス型高速撹拌装置(コーレス型
羽根・直径70mm)を使用して、未加工コーンスター
チ225gを温水に溶解し、図−1に示す方法で製糊を
行った。なお、製糊終了後の保存は、39℃の恒温槽に
て低速撹拌機(3枚プロペラ羽根2段・直径70mmで
400rpm)を使用して行った。各添加薬品の重量
(g)、倍水比および製糊時の回転条件は以下の通りで
ある。 25%カセイソーダ 硼 酸 倍 水 周速m/min(回転数rpm) 1−a 25.40 2.93 3.3 660(3000) 硼酸+硼砂 1−b 25.40 2.28+1.0 3.3 660(3000)Example 1 225 g of unprocessed corn starch was dissolved in hot water using a Corless type high-speed agitator having a strong shearing force (Coleth type blade, diameter 70 mm), and paste was prepared by the method shown in FIG. It was In addition, storage after completion of the paste preparation was performed using a low-speed stirrer (3 propeller blades, 2 stages, diameter: 70 mm, 400 rpm) in a constant temperature bath at 39 ° C. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 25% caustic soda Boric acid Double water Peripheral speed m / min (rotation speed rpm) 1-a 25.40 2.93 3.3 660 (3000) Boric acid + borax 1-b 25.40 2.28 + 1.0 3.3 660 (3000)
【0022】比較例1 通常の低撹拌装置(3枚プロペラ羽根2段 70mm
径)を使用して、未加工コーンスターチ200gを温水
に溶解し、図−2に示す方法で製糊を行う。保存は実施
例と同様の方法である。各添加薬品の重量(g)、倍水
比および製糊時の回転条件は以下の通りである。 5.2%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 105 2.60 3.3 98.9(450)Comparative Example 1 Ordinary low agitation device (3 propeller blades 2 stages 70 mm
(Diameter) is used to dissolve 200 g of raw corn starch in warm water and paste is prepared by the method shown in FIG. The storage is the same as in the example. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 5.2% caustic soda Boric acid Double water ratio Peripheral speed m / min (rpm) 105 2.60 3.3 98.9 (450)
【0023】実施例2 未加工タピオカ澱粉225gを温水に溶解し、実施例1
と同様の方法で製糊を行った。各添加薬品の重量
(g)、倍水比および製糊時の回転条件は以下の通りで
ある。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 24.12 2.93 3.3 660(3000)Example 2 225 g of raw tapioca starch was dissolved in warm water to prepare Example 1
A paste was prepared in the same manner as in. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rotation speed rpm) 24.12 2.93 3.3 660 (3000)
【0024】比較例2 未加工タピオカ澱粉200gを温水に溶解し、比較例1
と同様に製糊を行った。各添加薬品の重量(g)、倍水
比および製糊時の回転条件は以下の通りである。 4.75%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 105 2.60 3.3 98.9(450)Comparative Example 2 200 g of raw tapioca starch was dissolved in warm water to prepare Comparative Example 1
Paste was prepared in the same manner as in. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 4.75% caustic soda Boric acid Double water ratio Peripheral speed m / min (rotation speed rpm) 105 2.60 3.3 98.9 (450)
【0025】実施例3 四級陽性澱粉(タピオカベース、糊化開始温度45.0
℃)4.5gと未加工コーンスターチ(糊化開始温度5
2.0℃、以下に使用する未加工コーンスターチはいず
れも同じである。)220.5gを配合(配合比2:9
8)して温水に溶解し、実施例1と同様の方法で製糊を
行った。各添加薬品の重量(g)、倍水比および製糊時
の回転条件は以下の通りである。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 25.15 2.93 3.3 660(3000)Example 3 Quaternary positive starch (tapioca base, gelatinization starting temperature 45.0)
4.5 g) and raw corn starch (gelatinization start temperature 5
The raw corn starch used at 2.0 ° C. and below is the same. ) 220.5 g was compounded (compounding ratio 2: 9
8) Then, it was dissolved in warm water and glue was prepared in the same manner as in Example 1. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rotation speed rpm) 25.15 2.93 3.3 660 (3000)
【0026】比較例3 四級陽性澱粉(タピオカベース、糊化開始温度45℃)
4gと未加工コーンスターチ196gを配合(配合比
2:98)して温水に溶解し、比較例1と同様に製糊を
行った。各添加薬品の重量(g)、倍水比および製糊時
の回転条件は以下の通りである。 5.2%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 105 2.60 3.3 98.9(450)Comparative Example 3 Quaternary positive starch (tapioca base, gelatinization starting temperature 45 ° C.)
4 g and 196 g of unprocessed corn starch were blended (blending ratio 2:98), dissolved in warm water, and glued in the same manner as in Comparative Example 1. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 5.2% caustic soda Boric acid Double water ratio Peripheral speed m / min (rpm) 105 2.60 3.3 98.9 (450)
【0027】実施例4 四級陽性澱粉(馬澱ベース、糊化開始温度34.5℃)
13.5gと未加工コーンスターチ211.5gを配合
(配合比6:94)して温水に溶解し、実施例1と同様
の方法で3.3倍水の製糊を行った(4−a)。また、
上記陽性澱粉15gと未加工コーンスターチ235gを
配合(配合比6:94)して温水に溶解し、実施例1と
同様の方法で2.5倍水の製糊を行った(4−b)。各
添加薬品の重量(g)、倍水比および回転条件は以下の
通りである。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 4−a 25.15 2.93 3.3 660(3000) 4−b 25.25 3.25 2.5 660(3000)Example 4 Quaternary positive starch (horse starch base, gelatinization starting temperature 34.5 ° C.)
13.5 g and 211.5 g of unprocessed corn starch were blended (blending ratio 6:94), dissolved in warm water, and a 3.3 times water paste was prepared in the same manner as in Example 1 (4-a). . Also,
15 g of the above positive starch and 235 g of unprocessed corn starch were mixed (mixing ratio 6:94) and dissolved in warm water, and 2.5 times water was used for sizing in the same manner as in Example 1 (4-b). The weight (g), double water ratio, and rotation condition of each additive chemical are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rotation speed rpm) 4-a 25.15 2.93 3.3 660 (3000) 4-b 25.25 3.25 2.5 660 (3000)
【0028】比較例4 四級陽性澱粉(馬澱ベース、糊化開始温度34.5℃)
12gと未加工コーンスターチ188gを配合(配合比
6:94)して温水に溶解し、比較例1と同様に製糊を
行った。各添加薬品の重量(g)、倍水比および製糊時
の回転条件は以下の通りである。 5.2%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 105 2.60 3.3 98.9(450)Comparative Example 4 Quaternary positive starch (horse starch base, gelatinization starting temperature 34.5 ° C.)
12 g and 188 g of unprocessed corn starch were blended (blending ratio 6:94), dissolved in warm water, and glued in the same manner as in Comparative Example 1. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 5.2% caustic soda Boric acid Double water ratio Peripheral speed m / min (rpm) 105 2.60 3.3 98.9 (450)
【0029】実施例5 両性澱粉(タピオカベース、糊化開始温度42.6℃)
13.5gと未加工コーンスターチ211.5gを配合
(配合比6:94)して温水に溶解し、実施例1と同様
の方法で製糊を行った。各添加薬品の重量(g)、倍水
比および製糊時の回転条件は以下の通りである。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 26.04 2.93 3.3 660(3000)Example 5 Amphoteric starch (tapioca base, gelatinization starting temperature 42.6 ° C.)
13.5 g and 211.5 g of unprocessed corn starch were blended (blending ratio 6:94), dissolved in warm water, and glued in the same manner as in Example 1. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rotation speed rpm) 26.04 2.93 3.3 660 (3000)
【0030】実施例6 尿素燐酸化澱粉(コンスベース、糊化開始温度35.5
℃)13.5gと未加工コーンスターチ211.5gを
配合(配合比6:94)して温水に溶解し、実施例1と
同様の方法で製糊を行った。各添加薬品の重量(g)、
倍水比および回転条件は以下の通りである。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 26.13 2.93 3.3 660(3000)Example 6 Urea phosphorylated starch (cons base, gelatinization starting temperature 35.5)
(° C) 13.5 g and raw corn starch 211.5 g were blended (blending ratio 6:94), dissolved in warm water, and glued in the same manner as in Example 1. Weight of each additive chemical (g),
The double water ratio and rotation conditions are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rpm) 26.13 2.93 3.3 660 (3000)
【0031】実施例7 低粘度化四級陽性澱粉(タピオカベース、糊化開始温度
44.5℃)15gと未加工コーンスターチ235gを
配合(配合比6:94)して温水に溶解し、実施例1と
同様の方法で製糊を行った。各添加薬品の重量(g)、
倍水比および製糊時の回転条件は以下の通りである。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 23.91 3.25 2.5 660(3000)Example 7 15 g of a low viscosity quaternary positive starch (tapioca base, gelatinization starting temperature 44.5 ° C.) and 235 g of unprocessed corn starch were mixed (mixing ratio 6:94) and dissolved in warm water. Gluing was performed in the same manner as in 1. Weight of each additive chemical (g),
The water doubling ratio and the rotation conditions at the time of paste making are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rpm) 23.91 3.25 2.5 660 (3000)
【0032】実施例8 低粘度化尿素燐酸化澱粉(コンスベース糊化開始温度3
2.3℃)37.5gと未加工コーンスターチ212.
5gを配合(配合比15:85)して温水に溶解し、実
施例1と同様の方法で製糊を行った。各添加薬品の重量
(g)、倍水比および製糊時の回転条件は以下の通りで
ある。 25%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 25.27 3.25 2.5 660(3000)Example 8 Low-viscosity urea-phosphorylated starch (cons base gelatinization starting temperature 3
2.3 ° C.) 37.5 g and raw corn starch 212.
5 g was blended (blending ratio 15:85), dissolved in warm water, and glued in the same manner as in Example 1. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 25% caustic soda Boric acid Double water ratio Peripheral speed m / min (rotation speed rpm) 25.27 3.25 2.5 660 (3000)
【0033】実施例9 四級陽性澱粉(タピオカベース、糊化開始温度45℃)
と未加工コーンスターチを配合比2:98でブレンドし
たもの(500kg)を実機テストに供した。攪拌には
従来の低攪拌機と強剪断力を有する高速攪拌機(歯付き
円板型羽根、直径170mm、1900m/minの周
速)を併用した。製糊方法としては、攪拌機の回転数を
3550rpmとしカセイソーダの濃度を9.1w/w
%に変えたほかはほぼ図−1に示す手順に従った。 9.1%カセイソーダ 硼 酸 硼 砂 倍水比 周速m/min(回転数rpm) 165kg 6.0kg 2.0kg 3.3 280(300) 1900(3550)Example 9 Quaternary positive starch (tapioca base, gelatinization starting temperature 45 ° C.)
A blend (500 kg) of corn starch and unprocessed corn starch was blended at a compounding ratio of 2:98, and subjected to an actual machine test. For stirring, a conventional low stirrer and a high speed stirrer having strong shearing force (toothed disc type blade, diameter 170 mm, peripheral speed of 1900 m / min) were used together. As the paste making method, the rotation number of the stirrer was 3550 rpm and the concentration of caustic soda was 9.1 w / w.
The procedure was almost as shown in Fig. 1 except that the percentage was changed. 9.1% caustic soda Boric acid Borax Double water ratio Peripheral speed m / min (rotation speed rpm) 165kg 6.0kg 2.0kg 3.3 280 (300) 1900 (3550)
【0034】比較例5 実施例9で行なった製糊装置において四級陽性澱粉(タ
ピオカベース、糊化開始温度45℃)と未加工コーンス
ターチを配合比2:98でブレンドしたもの(500
g)を低攪拌機のみを使用して実機テストに供した。Comparative Example 5 A mixture of quaternary positive starch (tapioca base, gelatinization starting temperature 45 ° C.) and unprocessed corn starch in the paste making apparatus used in Example 9 at a compounding ratio of 2:98 (500
g) was subjected to an actual machine test using only a low stirrer.
【0035】比較例6 アルファー化澱粉(タピオカベース)12gと未加工コ
ーンスターチ188gを配合(配合比6:94)し、図
−3に示す方法で製糊を行った。製糊装置や保存方法は
比較例1と同様である。各添加薬品の重量(g)、倍水
比および製糊時の回転条件は以下の通りである。 5.2%カセイソーダ 硼 酸 倍水比 周速m/min(回転数rpm) 105 2.60 3.3 98.9(450)Comparative Example 6 12 g of alferized starch (tapioca base) and 188 g of unprocessed corn starch were mixed (mixing ratio 6:94), and paste was prepared by the method shown in FIG. The pasting device and the storage method are the same as in Comparative Example 1. The weight (g) of each additive chemical, the water doubling ratio, and the rotation conditions during paste making are as follows. 5.2% caustic soda Boric acid Double water ratio Peripheral speed m / min (rpm) 105 2.60 3.3 98.9 (450)
【0036】各実施例および比較例で得られた結果を表
1に示す。The results obtained in each Example and Comparative Example are shown in Table 1.
【表1】 [Table 1]
【0037】表1にみられる通り、本発明の製糊方法に
よれば、同一原料・同一配合において従来の製糊方法に
比べはるかに製糊が簡単であり、且つ、得られた接着剤
糊液は常態接着性を従来方法による接着剤糊液と同等に
保ちながら、流動性や初期接着性が大幅に向上したもの
である。配合比や原料を適当に選ぶことで低倍水化も実
現できた。これらのことから本発明による接着剤糊液は
高速貼合にも十分対応が可能なことが判る。As shown in Table 1, according to the pasting method of the present invention, the pasting method is much easier than the conventional pasting method with the same raw material and the same composition, and the obtained adhesive paste is obtained. The liquid has substantially improved fluidity and initial adhesiveness, while maintaining the normal adhesiveness to be equal to that of the conventional adhesive paste liquid. By properly selecting the compounding ratio and raw materials, we were able to achieve low water doubling. From these facts, it is understood that the adhesive glue solution according to the present invention can sufficiently cope with high-speed bonding.
【図1】本発明の製糊方法の一例を示す。FIG. 1 shows an example of a sizing method of the present invention.
【図2】従来の製糊方法の一例を示す。FIG. 2 shows an example of a conventional pasting method.
【図3】従来の製糊方法の他の一例を示す。FIG. 3 shows another example of a conventional pasting method.
Claims (2)
加えて全体の澱粉を部分膨潤状態にし、次いで硼酸また
は硼酸と硼砂を加えることによって膨潤を停止して適度
な粘度を有する段ボール用接着剤を得る工程を含むノー
キャリア方式による製糊方法において、500m/mi
n以上の周速を有する強力撹拌手段で剪断をかけながら
上記部分膨潤化および膨潤停止を行うことを特徴とする
段ボール用澱粉接着剤の製糊方法。1. A corrugated board having an appropriate viscosity by adding an excessive amount of alkali to an aqueous starch suspension to partially swell the whole starch and then adding boric acid or boric acid and borax to stop the swelling. In a no-carrier type sizing method including a step of obtaining an adhesive, 500 m / mi
A method for making a starch adhesive for corrugated board, which comprises performing the partial swelling and the swelling stop while applying shearing with a strong stirring means having a peripheral speed of n or more.
温度が未加工澱粉に対し5℃以上低い加工澱粉を未加工
澱粉に対して1〜30重量%配合してなる澱粉を用いる
請求項1記載の製糊方法。2. The starch according to claim 1, wherein a starch prepared by blending 1 to 30% by weight of a processed starch with a gelatinization start temperature in an alkaline amylograph lower than that of the unprocessed starch by 5 ° C. or more is used. Glue method.
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JP6155327A JP2954834B2 (en) | 1994-06-13 | 1994-06-13 | Gluing method of starch adhesive for corrugated cardboard |
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JP6155327A JP2954834B2 (en) | 1994-06-13 | 1994-06-13 | Gluing method of starch adhesive for corrugated cardboard |
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JPH07331202A true JPH07331202A (en) | 1995-12-19 |
JP2954834B2 JP2954834B2 (en) | 1999-09-27 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000309765A (en) * | 1999-04-27 | 2000-11-07 | Nippon Starch Chemical Co Ltd | Adhesive composition |
JP2002226809A (en) * | 2001-01-31 | 2002-08-14 | Rengo Co Ltd | Starch paste for corrugated cardboard lamination |
JP2005179586A (en) * | 2003-12-22 | 2005-07-07 | Oji Cornstarch Co Ltd | Adhesive for use in heat-saving lamination |
JP2009138128A (en) * | 2007-12-07 | 2009-06-25 | Oji Cornstarch Co Ltd | Formaldehyde-free and water-resistant adhesive for corrugated cardboard |
-
1994
- 1994-06-13 JP JP6155327A patent/JP2954834B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000309765A (en) * | 1999-04-27 | 2000-11-07 | Nippon Starch Chemical Co Ltd | Adhesive composition |
JP2002226809A (en) * | 2001-01-31 | 2002-08-14 | Rengo Co Ltd | Starch paste for corrugated cardboard lamination |
JP2005179586A (en) * | 2003-12-22 | 2005-07-07 | Oji Cornstarch Co Ltd | Adhesive for use in heat-saving lamination |
JP4527972B2 (en) * | 2003-12-22 | 2010-08-18 | 王子コーンスターチ株式会社 | Heat-saving adhesive for bonding |
JP2009138128A (en) * | 2007-12-07 | 2009-06-25 | Oji Cornstarch Co Ltd | Formaldehyde-free and water-resistant adhesive for corrugated cardboard |
Also Published As
Publication number | Publication date |
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JP2954834B2 (en) | 1999-09-27 |
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