JPS5920699B2 - Method for producing thermoplastic fibers with adhesive ability - Google Patents
Method for producing thermoplastic fibers with adhesive abilityInfo
- Publication number
- JPS5920699B2 JPS5920699B2 JP50018569A JP1856975A JPS5920699B2 JP S5920699 B2 JPS5920699 B2 JP S5920699B2 JP 50018569 A JP50018569 A JP 50018569A JP 1856975 A JP1856975 A JP 1856975A JP S5920699 B2 JPS5920699 B2 JP S5920699B2
- Authority
- JP
- Japan
- Prior art keywords
- pva
- fibers
- melt
- adhesive
- plasticizer
- 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
Links
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
Description
【発明の詳細な説明】
本発明は水及び熱で接着性能を発揮する再湿ホットメル
ト接着性成形物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a rewetting hot-melt adhesive molded product that exhibits adhesive performance with water and heat.
従来、ポリビニルアルコール(以下PVAと略。記する
。)は、その分子構造において強力な分子間水素結合を
有するため熱溶融しにくく、さらに結晶領域の融点が分
解温度に近いため溶融と同時に分解が起り溶融押出成形
が困難であつた。そのためPVAの溶融押出成形に際し
ては水等の可塑剤を多量に混合して溶融するか、あるい
は特公昭38−10362号公報に提案されているよう
な特殊な条件下でしか溶融押出成形はできなかつた。し
かるに前者は多量の可塑剤を必要とするため得られる成
形物は、例えば水を使用する場合成形物表面に水の沸騰
により発泡跡が残り、また多価アルコール等の可塑剤を
使用した場合、該可塑剤が成形物表面ににじみ出る等の
問題があり、通常の汎用熱可塑性樹脂のような溶融押出
成形はできなかつた。Conventionally, polyvinyl alcohol (hereinafter abbreviated as PVA) has a strong intermolecular hydrogen bond in its molecular structure, which makes it difficult to melt under heat.Furthermore, since the melting point of the crystalline region is close to the decomposition temperature, it decomposes at the same time as it melts. This made melt extrusion molding difficult. Therefore, when melt-extruding PVA, it is only possible to melt it by mixing a large amount of plasticizer such as water, or under special conditions as proposed in Japanese Patent Publication No. 38-10362. Ta. However, the former requires a large amount of plasticizer, so if water is used, the resulting molded product will leave foam marks on the surface of the molded product due to boiling of water, and if a plasticizer such as polyhydric alcohol is used, There were problems such as the plasticizer oozing out onto the surface of the molded product, and it was not possible to perform melt extrusion molding as with ordinary general-purpose thermoplastic resins.
従つてPVAと多量の可塑剤を併用する溶融押出成形は
従来の溶融押出成形と区別して半溶融押出成形と称し、
個有の技術が確立されている。一方、後者は平均重合度
1000以上のPVAを空気を排除した状態又は不活性
気体中でかつ加圧下に溶融紡糸するものであるが、この
場合の溶融温度はPVAの分解温度に近い高温でかつ、
かなりの高圧を必要としていること、さらに溶融粘度が
高いことから工業的には実施不可能に近いものである。Therefore, melt extrusion molding that uses PVA and a large amount of plasticizer in combination is called semi-melt extrusion molding to distinguish it from conventional melt extrusion molding.
Unique technology has been established. On the other hand, in the latter method, PVA with an average degree of polymerization of 1000 or more is melt-spun under pressure in a state excluding air or in an inert gas, but in this case, the melting temperature is high and close to the decomposition temperature of PVA. ,
It is almost impossible to implement industrially because it requires considerably high pressure and has a high melt viscosity.
したがつて、PVA系成形物の製造法は、現在PVA水
溶液からの湿式及び乾式紡糸、水及びその他の可塑剤を
併用する半溶融押出成形が採用されているにすぎないの
である。Therefore, the current methods for manufacturing PVA-based moldings are only wet and dry spinning from an aqueous PVA solution and semi-melt extrusion using water and other plasticizers.
すなわち、PVA系繊維の製造に際し、PVA単独又は
PVAに対し5重量%以下の少量の可塑剤を使用して汎
用の熱可塑性樹脂の溶融押出成形と同様に溶融押出成形
することは不可能であつたのである。一方、PVA系成
形物すなわちPVA系繊維及びフィルムは従来から衣料
用、産業資材用などに広く利用されているが、さらに特
殊な用途に利用される水溶性繊維、及びフィルム、水又
は熱水膨潤性繊維がある。That is, when producing PVA-based fibers, it is impossible to perform melt extrusion molding using PVA alone or using a small amount of plasticizer of 5% by weight or less relative to PVA in the same way as melt extrusion molding of general-purpose thermoplastic resins. It was. On the other hand, PVA-based molded products, that is, PVA-based fibers and films, have been widely used for clothing, industrial materials, etc., but water-soluble fibers and films used for more special purposes, water or hot water swelling There are sexual fibers.
すなわち、PVAの吸湿吸水性を利用した接着性能を有
する成形物であるが、いずれも水を利用して接着性能を
発揮するものであり、熱溶融して接着性能を発揮するも
のではなかつた。本発明者らは、水及び熱で接着性能を
発揮する再湿ホットメルト接着性成形物について種々研
究した結果、従来のPVAではかかる性能が得られない
が、平均重合度50〜300で、かつ残存酢酸基15〜
80モル%のPVAが再湿ホットメルト接着能を有し、
さらにかかる特殊なPVAが単独ででも溶融しうるし、
またPVAに対し5重量%の可塑剤を用いても溶融しう
るという事実及び可塑剤の使用量がPVAに対し5重量
%以下の場合には得られる成形物の表面に可塑剤がにじ
み出る等の問題がないという事実を見い出し、本発明を
完成した。That is, although these are molded products that have adhesive performance that utilizes the hygroscopicity of PVA, all of them utilize water to exhibit adhesive performance, and do not exhibit adhesive performance by being thermally melted. The present inventors have conducted various studies on re-wet hot melt adhesive molded products that exhibit adhesive performance with water and heat, and have found that although conventional PVA cannot achieve such performance, it has an average degree of polymerization of 50 to 300, and Residual acetate group 15~
80 mol% PVA has rewet hot melt adhesive ability;
Furthermore, such special PVA can be melted alone,
Furthermore, the fact that PVA can be melted even if 5% by weight of plasticizer is used, and if the amount of plasticizer used is less than 5% by weight based on PVA, the plasticizer may ooze out on the surface of the resulting molded product. They discovered that there is no problem and completed the present invention.
すなわち本発明は平均重合度50〜300、残存酢酸基
15〜80モル%のPVAと、PVAに対しO〜5重量
%の可塑剤とからなる再湿接着性能及び熱溶融接着性能
を有する再湿ホツト接着成形物である。In other words, the present invention provides a rewetting material having rewetting adhesive performance and heat melt adhesive performance, which is composed of PVA having an average degree of polymerization of 50 to 300, residual acetic acid groups of 15 to 80 mol%, and a plasticizer of 0 to 5% by weight based on the PVA. It is a hot adhesive molded product.
本発明について詳細に説明する。The present invention will be explained in detail.
本発明に用いるPVAは、平均重合度が50〜300で
、かつ残存酢酸基が15〜80モル%のものであり、か
かるPVAは140〜200℃で完全に溶融流動し、曳
糸性を有する。The PVA used in the present invention has an average degree of polymerization of 50 to 300 and a residual acetic acid group of 15 to 80 mol%, and such PVA completely melts and flows at 140 to 200°C and has stringiness. .
平均重合度が50未満になると曳糸性、繊維及びフイル
ムの可撓性が極端に低下し、繊維及びフイルムの形成が
困難となる。重合度が300をこえる場合は溶融温度及
び粘度が高くなりすぎ、やはり可紡性が低下し、またフ
イルムの形成も困難となる。残存酢酸基が15モル%未
満では溶融しにくくなり、80モル%をこえる場合は粘
着性が増し、繊維間で接着が生ずるようになる。したが
つて、PVAとしては平均重合度50〜300、残存酢
酸基15〜80モル%のものが適している。これらのP
VAは、十分に乾燥すれば、通常の溶融紡糸機で溶融押
出成形することができる。If the average degree of polymerization is less than 50, the spinnability and flexibility of fibers and films will be extremely reduced, making it difficult to form fibers and films. If the degree of polymerization exceeds 300, the melting temperature and viscosity will become too high, resulting in poor spinnability and difficulty in forming a film. If the residual acetate group is less than 15 mol%, it will be difficult to melt, and if it exceeds 80 mol%, the adhesiveness will increase and adhesion will occur between the fibers. Therefore, PVA having an average degree of polymerization of 50 to 300 and a residual acetate group of 15 to 80 mol% is suitable. These P
Once sufficiently dried, VA can be melt extruded on a conventional melt spinning machine.
その場合温度、速度などの溶融押出条件は使用するPV
Aの平均重合度、残存酢酸基によつて決定すればよい。
また、紡糸繊維及び形成フイルムは従来法によるPVA
繊維及びフイルムのように乾燥する必要がなく、通常の
溶融押出熱可塑性樹脂成形物と同様に油剤処理あるいは
延伸することもできる。溶融押出成形に際しては、前記
特殊PVA単独で十分良好な成形物を有するが、特に必
要あればポリエチレングリコールなどの多価アルコール
、尿素誘導体などの可塑剤を使用してもよい。In that case, melt extrusion conditions such as temperature and speed should be determined based on the PV used.
It may be determined based on the average degree of polymerization of A and the remaining acetic acid groups.
In addition, the spun fibers and formed film are made of PVA using conventional methods.
Unlike fibers and films, it does not need to be dried, and can be treated with oil or stretched in the same way as ordinary melt-extruded thermoplastic resin moldings. In melt extrusion molding, the special PVA alone produces a sufficiently good molded product, but if particularly necessary, a polyhydric alcohol such as polyethylene glycol or a plasticizer such as a urea derivative may be used.
しかし可塑剤の添加量が5重量%をこえると得られる成
形物の表面ににじみでる等の問題があり、さらに成形物
の性能も低下するので5重量%以下にすることが必要で
ある。このようにして得られる本発明のPVA系成形物
は良好な接着性を有する。However, if the amount of plasticizer added exceeds 5% by weight, there will be problems such as bleeding on the surface of the resulting molded product, and the performance of the molded product will also deteriorate, so it is necessary to limit the amount to 5% by weight or less. The PVA-based molded product of the present invention obtained in this manner has good adhesive properties.
特に平均重合度50〜300、残存酢酸基15〜40モ
ル%の成形物は熱で接着すると同時に、容易に水に溶け
るので、水及び水蒸気処理で接着能を発揮せしめること
ができる。また残存酢酸基が40〜80モル%の繊維は
水でも水蒸気でも、さらには熱だけでも接着能を発揮す
る。たとえば本発明により得られたPVA繊維を適当な
繊維長にカツトし、開繊し、これを天然繊維あるいは合
成繊維と混紡し、ローラ間で熱圧すると天然繊維あるい
ほ合成繊維間を接着させることができるし、通常の水溶
性PVA繊維(ビニロンバインダ一)では十分な接着が
得にくい疎水性繊維に対しても本発明により得られた繊
維は効果的に接着能を発揮する。In particular, a molded product having an average degree of polymerization of 50 to 300 and a residual acetic acid group of 15 to 40 mol% can be bonded by heat and at the same time be easily soluble in water, so that it can exhibit its adhesive ability when treated with water or steam. Furthermore, fibers containing 40 to 80 mol% of residual acetic acid groups exhibit adhesive ability with water, steam, or even heat alone. For example, the PVA fibers obtained according to the present invention are cut to an appropriate fiber length, opened, blended with natural fibers or synthetic fibers, and heated and pressed between rollers to bond the natural fibers or synthetic fibers together. Furthermore, the fibers obtained according to the present invention exhibit effective adhesion ability even to hydrophobic fibers to which it is difficult to obtain sufficient adhesion with ordinary water-soluble PVA fibers (vinylon binder).
これらのことかられかるように本発明の成形物は接着性
成形物として非常に広範囲に利用しうるものである。以
下、実施例により本発明をさらに詳細に説明する。As can be seen from these facts, the molded product of the present invention can be used in a very wide range of applications as an adhesive molded product. Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例 1
平均重合度79で残存酢酸基が42モル%のチツプ状P
VAを減圧下、60℃で十分に乾燥したのち、150℃
で内径3011φ、長さ45011のエクストルーダ一
を用い、溶融し、孔径0.6nφ、40孔数のノズルで
、吐出量8y/駆、紡糸速度500m/71wtで紡糸
した。Example 1 Chip-shaped P with an average degree of polymerization of 79 and residual acetic acid groups of 42 mol%
After thoroughly drying VA at 60°C under reduced pressure, dry it at 150°C.
Using an extruder with an inner diameter of 3011φ and a length of 45011 mm, the material was melted and spun using a nozzle with a hole diameter of 0.6nφ and 40 holes at a discharge rate of 8y/drive and a spinning speed of 500m/71wt.
得られた繊維は淡黄、透明で繊度3.2デニール、強度
1.6f/d、伸度20.8%であつた。このようにし
て得られたPVA繊維を繊維長511にカツトし、2枚
のポリプロピレン繊維不織布の間にばらまき、130℃
のアイロンで10秒間押しつけると不織布間で接着し、
その接着性は良好であつた。また、該不織布に50℃の
温水を噴霧し、ローラーで圧着したところ不織布間で接
着した。実施例 2
平均重合度170、残存酢酸基25モル%のPVAチツ
ブを200℃で実施例1と同じエクストルーダ一を用い
、孔径0.5mmφのノズルから1孔当り吐出量0.3
V/mで吐出し、1000m/mで巻取つた。The obtained fibers were pale yellow and transparent, and had a fineness of 3.2 denier, a strength of 1.6 f/d, and an elongation of 20.8%. The PVA fibers obtained in this way were cut to a fiber length of 511, spread between two sheets of polypropylene fiber nonwoven fabric, and heated at 130°C.
If you press it with an iron for 10 seconds, it will adhere between the non-woven fabrics,
Its adhesion was good. Further, when hot water at 50° C. was sprayed onto the nonwoven fabrics and the nonwoven fabrics were pressed together with a roller, the nonwoven fabrics were bonded together. Example 2 A PVA chip with an average degree of polymerization of 170 and a residual acetic acid group of 25 mol % was heated at 200°C using the same extruder as in Example 1, and the discharge amount per hole was 0.3 from a nozzle with a hole diameter of 0.5 mmφ.
It was discharged at V/m and wound up at 1000 m/m.
このようにして得たPVA繊維は単繊維デニール約2デ
ニール、強度2.21V/d、伸度33.5%であつた
。このPVA繊維を511の長さに切断し、スフモスの
基布とアルミ箔間にばらまき、190℃のアイロンを圧
着したところ、良好なヒートシール性を示した。また、
水蒸気処理をして圧着した場合も良好な接着が得られた
。The PVA fiber thus obtained had a single fiber denier of about 2 deniers, a strength of 2.21 V/d, and an elongation of 33.5%. When this PVA fiber was cut into 511 lengths, spread between a sfumos base fabric and aluminum foil, and pressed with an iron at 190° C., it showed good heat sealability. Also,
Good adhesion was also obtained when pressure bonded after steam treatment.
実施例 3
平均重合度275、残存酢酸基72モル%のPVAチツ
プを200℃で実施例2と同様に溶融紡糸し、単繊維繊
度が1.6デニール、強度1.847/d、伸度18.
3%のPVA繊維を得た。Example 3 PVA chips with an average degree of polymerization of 275 and a residual acetate group of 72 mol% were melt-spun at 200°C in the same manner as in Example 2, and the single fiber fineness was 1.6 denier, strength was 1.847/d, and elongation was 18. ..
3% PVA fibers were obtained.
この繊維を2枚のポリエステル不織布間にばらまき20
0℃に加熱したローラー間を通すことによりポリエステ
ル不織布の張り合せができた。同不織布に水を散布し、
ローラーを通し乾燥したところ良好な接着性を有する張
り合せができた。Spread these fibers between two sheets of polyester nonwoven fabric for 20 minutes.
The polyester nonwoven fabric was laminated by passing it between rollers heated to 0°C. Spray water on the same nonwoven fabric,
When dried by passing it through a roller, a bond with good adhesion was obtained.
実施例4、比較例1平均重合度250、残存酢酸基20
モル%のPVAlOO重量部に対しグリセリン3重量部
を含むチツプ状PVAを減圧下70℃で十分に乾燥した
のち、スクリユ一径115〜(L/D=20)の押出機
にてTダイより幅500〜、厚さ40μのフイルムを周
速100m/分で回転しているローラー上に押出し、冷
却して巻き取つた。Example 4, Comparative Example 1 Average degree of polymerization 250, residual acetate group 20
Chip-shaped PVA containing 3 parts by weight of glycerin per mol% of PVAlOO is thoroughly dried at 70°C under reduced pressure, and then cut into widths from a T-die using an extruder with a screw diameter of 115~ (L/D=20). A film having a thickness of 40 μm and 500 μm was extruded onto a roller rotating at a circumferential speed of 100 m/min, cooled, and wound up.
押出機のTダイの温度は200℃とし、スクリユ一回転
数は120rpmとした。得られたフイルムは可塑剤の
グリセリンがにじみでてくることもなく、透明で、24
0kg/Cdの強力で伸度は180%であり、30℃の
水中で容易に溶解するものであつた。The temperature of the T-die of the extruder was 200° C., and the number of revolutions of the screw was 120 rpm. The obtained film did not ooze out the plasticizer glycerin and was transparent.
It had a strength of 0 kg/Cd, an elongation of 180%, and was easily soluble in water at 30°C.
このフイルムを実施例1に使用したポリプロピレン繊維
不織布の間に入れ160℃のアイロンで押しつけたとこ
ろ、該不織布は強固に接着された。When this film was placed between the polypropylene fiber nonwoven fabrics used in Example 1 and pressed together with an iron at 160°C, the nonwoven fabrics were firmly adhered.
Claims (1)
ル%のポリビニルアルコールと、ポリビニルアルコール
に対し0〜5重量%の可塑剤とからなる再湿接着性能及
び熱溶融接着性能を有する再湿ホットメルト接着性成形
物。1. A rewetting hot adhesive having rewetting adhesive performance and heat melting adhesive performance, which is composed of polyvinyl alcohol with an average degree of polymerization of 50 to 300, residual acetic acid groups of 15 to 80 mol%, and a plasticizer of 0 to 5% by weight based on the polyvinyl alcohol. Melt adhesive molded product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50018569A JPS5920699B2 (en) | 1975-02-13 | 1975-02-13 | Method for producing thermoplastic fibers with adhesive ability |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50018569A JPS5920699B2 (en) | 1975-02-13 | 1975-02-13 | Method for producing thermoplastic fibers with adhesive ability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5195440A JPS5195440A (en) | 1976-08-21 |
| JPS5920699B2 true JPS5920699B2 (en) | 1984-05-15 |
Family
ID=11975245
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50018569A Expired JPS5920699B2 (en) | 1975-02-13 | 1975-02-13 | Method for producing thermoplastic fibers with adhesive ability |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5920699B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2785350B2 (en) * | 1989-07-06 | 1998-08-13 | エヌオーケー株式会社 | Adhesive for vinyl alcohol resin film |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5177632A (en) * | 1974-12-27 | 1976-07-06 | Sekisui Chemical Co Ltd | NETSUYOJUGATASETSUCHAKUZAISOSEIBUTSU |
-
1975
- 1975-02-13 JP JP50018569A patent/JPS5920699B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5195440A (en) | 1976-08-21 |
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