JPS63235558A - Steaming adhesive nonwoven cloth and its production - Google Patents
Steaming adhesive nonwoven cloth and its productionInfo
- Publication number
- JPS63235558A JPS63235558A JP62071141A JP7114187A JPS63235558A JP S63235558 A JPS63235558 A JP S63235558A JP 62071141 A JP62071141 A JP 62071141A JP 7114187 A JP7114187 A JP 7114187A JP S63235558 A JPS63235558 A JP S63235558A
- Authority
- JP
- Japan
- Prior art keywords
- component
- fibers
- nonwoven fabric
- evoh
- fiber
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000853 adhesive Substances 0.000 title description 4
- 230000001070 adhesive effect Effects 0.000 title description 4
- 239000004744 fabric Substances 0.000 title description 2
- 238000010025 steaming Methods 0.000 title 1
- 239000000835 fiber Substances 0.000 claims description 68
- 239000004745 nonwoven fabric Substances 0.000 claims description 40
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 claims description 34
- 238000010438 heat treatment Methods 0.000 claims description 29
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 15
- 239000005977 Ethylene Substances 0.000 claims description 15
- 239000002131 composite material Substances 0.000 claims description 13
- 229920001169 thermoplastic Polymers 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 238000007127 saponification reaction Methods 0.000 claims description 5
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 29
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 28
- 239000000306 component Substances 0.000 description 18
- 238000002844 melting Methods 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 230000008018 melting Effects 0.000 description 13
- -1 i.e. Substances 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 239000000123 paper Substances 0.000 description 4
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002074 melt spinning Methods 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- RZXDTJIXPSCHCI-UHFFFAOYSA-N hexa-1,5-diene-2,5-diol Chemical compound OC(=C)CCC(O)=C RZXDTJIXPSCHCI-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Nonwoven Fabrics (AREA)
- Multicomponent Fibers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はエチレンビニルアルコール共重合体繊維を含む
不織布及びその製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a nonwoven fabric containing ethylene vinyl alcohol copolymer fibers and a method for producing the same.
(従来の技術)
エチレンビニルアルコール共重合体(以下EVOHと略
記する)を溶融紡糸してなる繊維は親水性に優れ”9こ
の繊維による織編物、不織布、は同じ目付の他の繊維に
よるものに比べ多量の水を抱水することができるうえ耐
薬品性、生体適合性。(Prior art) Fibers made by melt-spinning ethylene vinyl alcohol copolymer (hereinafter abbreviated as EVOH) have excellent hydrophilic properties.''9 Woven or knitted fabrics or non-woven fabrics made from this fiber are similar to those made from other fibers with the same basis weight. In addition to being able to hold a larger amount of water, it is chemically resistant and biocompatible.
化学反応性にも優れた性質をもっているので、広い用途
が期待されている。Because it has excellent chemical reactivity, it is expected to have a wide range of uses.
EVOHの親水性と融点の低さとはビニルアルコールと
エチレンの量によって逆の間係°がみられる。すなわち
ビニルアルコールが多くエチレンが少ないと親水性は増
すが融点が高く、ビニルアルコールが少なくエチレンが
多いと親水性は悪いが融点が下がるという関係である。There is an inverse relationship between EVOH's hydrophilicity and low melting point depending on the amount of vinyl alcohol and ethylene. That is, when vinyl alcohol is high and ethylene is low, hydrophilicity increases but the melting point is high, and when vinyl alcohol is low and ethylene is high, hydrophilicity is poor but the melting point is low.
不織布を製造する方法として構成繊維の一つに低融点繊
維を使用しこれを熱溶融して構成繊維間を接着する方法
があるが、EVOHm維を使いこ′の方法で不織布を製
造するとエチレンの量を多くしなければならず、目的と
する親水性が得にくい欠点があった。One method of producing nonwoven fabric is to use a low-melting point fiber as one of the constituent fibers and heat-melt it to bond the constituent fibers together. However, when producing nonwoven fabric using this method using EVOHm fibers, ethylene This had the drawback that the amount had to be increased, making it difficult to obtain the desired hydrophilicity.
そこで、特開昭57−66200により開示された技術
ではEVOH繊維に吸水させると繊維が膨潤するので融
点以下の温度でも湿熱接着が可能であるとされている。Therefore, in the technique disclosed in JP-A-57-66200, it is said that when EVOH fibers absorb water, the fibers swell, so that wet heat bonding is possible even at temperatures below the melting point.
しかし同技術は湿熱接着のためにEVOHm維が飽和吸
水率(30℃で水中 。However, with this technology, the EVOHm fiber has a saturated water absorption rate (in water at 30°C) due to wet heat adhesion.
24時間浸漬後の値)の70%以上吸水していることが
不可欠で、この条件下で始めて通常の乾燥条件でしかも
融点以下で湿熱接着が可能になっている。このため繊維
ウェブを熱処理する前に長時間水中に浸漬する必要があ
った。It is essential that the film absorbs 70% or more of the water (value after 24-hour immersion), and only under this condition is wet heat bonding possible under normal drying conditions and below the melting point. For this reason, it was necessary to immerse the fibrous web in water for a long time before heat treating it.
従って上記、特開昭57−66200による方法では抄
紙法による不織布、すなわち紙しか得られていない、湿
潤したEVOH繊維をカードにかけウェブにすることは
できないので、従来の吸水接着方法では嵩高性、柔軟性
のある不織布を得ることはできなかったのである。Therefore, with the above-mentioned method according to JP-A-57-66200, only non-woven fabric, i.e., paper, can be obtained by the papermaking method, and wet EVOH fibers cannot be made into a web by carding. Therefore, it was not possible to obtain a nonwoven fabric with good properties.
(発明が解決すべき問題点)
本発明はEVOH繊維を用い、繊維を湿式抄紙によらず
カードにより解繊してウェブを形成した後、繊維間を熱
融着した嵩高性、柔軟性のあるしかも十分な強力をもっ
た不織布を得ることを目的とするものである。(Problems to be Solved by the Invention) The present invention uses EVOH fibers, and after forming a web by defibrating the fibers with a card without using wet paper making, the fibers are thermally fused to form a bulky and flexible web. Furthermore, the purpose is to obtain a nonwoven fabric with sufficient strength.
(問題点を解決する手段)
本発明者等はEVOH繊維の特質に着目し、ポリビニル
アルコールとエチレンの割合がある範囲内において、不
織布として所望の親水性を得られ口&
、比較的低い温度でしかも繊維内に給水させずとも、濃
度の高い水蒸気があれば湿熱接着可能であることを見出
し1本発明に至った。(Means for Solving the Problems) The present inventors have focused on the characteristics of EVOH fibers, and found that within a certain range of polyvinyl alcohol and ethylene ratios, the desired hydrophilicity can be obtained as a nonwoven fabric, and at relatively low temperatures. Furthermore, the inventors discovered that wet heat bonding is possible even if water is not supplied into the fibers as long as there is a high concentration of water vapor, leading to the present invention.
すなわち1本発明の第1の発明は、エチレンモル比(E
モル%)が20≦E<55.ケン化度98%以上のエチ
レンビニルアルコール共重合体を第1成分、他の熱可塑
性重合体を第2成分とし。That is, the first aspect of the present invention is that the ethylene molar ratio (E
mol%) is 20≦E<55. An ethylene vinyl alcohol copolymer having a degree of saponification of 98% or more is used as the first component, and another thermoplastic polymer is used as the second component.
第1成分と第2成分の構成比が20 : 80〜80:
20の割合である複合繊維を30%以上含む繊維ウェブ
からなる湿熱接着不織布である。The composition ratio of the first component and the second component is 20:80 to 80:
This is a moisture-thermal bonded nonwoven fabric made of a fiber web containing 30% or more of composite fibers with a ratio of 20% or more.
EVOH繊維のエチレンモル比(E%)が20以上必要
である理由はEVOH繊維の紡糸性に問題があるからで
ある。E=20のときF、VOHの融点は207℃であ
り、5分以上滞留するとゲル化が始まる温度は240.
2℃と測定される。この範囲内で安定して溶融紡糸する
には融点より少なくとも2 (1’Cは高い温度すなわ
ち227℃は必要であるから、とり得る温度範囲は2i
o、2−227=13.2 (℃)と狭くなり、溶融紡
糸時に少なくともこの程度のとり得る温度範囲が望まし
いからであり、他の熱可塑性重合性と複合紡糸するにも
これ以上温度範囲が狭くては、安定に紡糸することが難
しいからである。The reason why the ethylene molar ratio (E%) of the EVOH fiber is required to be 20 or more is that there is a problem with the spinnability of the EVOH fiber. When E=20, the melting point of F and VOH is 207°C, and the temperature at which gelation begins when retained for 5 minutes or more is 240.
Measured at 2°C. To perform stable melt spinning within this range, a temperature at least 2 (1'C) higher than the melting point is required, i.e. 227°C, so the possible temperature range is 2i
o, 2-227 = 13.2 (°C), and it is desirable to have at least this possible temperature range during melt spinning, and a longer temperature range is required for composite spinning with other thermoplastic polymerizable materials. This is because if it is too narrow, it is difficult to perform stable spinning.
またEが大きいはどEVOHの融点は低くなるが、親水
性は悪くなるので2本発明の目的とする湿熱接着性繊維
を得るためE〈55とした。Furthermore, if E is large, the melting point of EVOH will be low, but the hydrophilicity will be poor. Therefore, in order to obtain the wet heat adhesive fiber which is the object of the present invention, E was set to 55.
EVOHのケン化度が98%以上である理由は98%よ
り低いと溶融樹脂が発泡しやすく紡糸工程で糸切れが多
くなるためである。The reason why the degree of saponification of EVOH is 98% or more is that if it is lower than 98%, the molten resin tends to foam and fiber breakage occurs frequently in the spinning process.
EVOHと複合繊維を作る他の熱可塑性樹脂はポリプロ
ピレン、ポリブチレンテレフタレート。Other thermoplastic resins that make EVOH and composite fibers are polypropylene and polybutylene terephthalate.
ナイロン6及びナイロン66が都合良く用いられ、ポリ
エチレンテレフタレートも適用できる。Nylon 6 and nylon 66 are conveniently used, and polyethylene terephthalate is also applicable.
E V OHは単独でも紡糸可能だが、繊維強力が弱く
紡糸工程上糸切れ等のトラブルも多いので。E V OH can be spun alone, but the fiber strength is weak and there are many problems such as thread breakage during the spinning process.
本発明では上記の熱可塑性樹脂との複合繊維を用いるが
、EVOH(第1成分)と他の熱可塑性重合体く第2成
分)の複合比を20 : 80〜8o:20としたのは
第1成分が20%未満では湿熱接着力が劣り、80%を
超える場合は繊維強力が劣るからである。 。In the present invention, a composite fiber with the above-mentioned thermoplastic resin is used, but the composite ratio of EVOH (first component) and other thermoplastic polymer (second component) is set to 20:80 to 8o:20. This is because if the content of one component is less than 20%, the wet heat adhesive strength will be poor, and if it exceeds 80%, the fiber strength will be poor. .
このような複合繊維を30%以上含む繊維ウェブは複合
繊維の融点以下の温度で湿熱接着することができる。3
0%以下でも不織布は形成できるが、不織布としての強
力が不足する。以下その製造方法について説明する。A fibrous web containing 30% or more of such composite fibers can be bonded with wet heat at a temperature below the melting point of the composite fibers. 3
Although a nonwoven fabric can be formed with less than 0%, the strength of the nonwoven fabric is insufficient. The manufacturing method will be explained below.
本発明の第2の発明は、エチレンモル比(Eモル%)が
20≦E<55.ケン化度が98%以上のエチレンビニ
ルアルコール恭重合体を第1成分、他の熱可塑性重合体
を第2成分とし、第1成分と第2成分の構成比が20:
80〜80 : 20のv1合である。?g合繊維を3
0%以上含む繊維ウェブを湿熱接着する不織布の製法に
おいて、該1a維ウエブにその重量の30%以上の水を
付与した後、該繊維ウェブの両面に接触する加熱体によ
り。The second aspect of the present invention is that the ethylene molar ratio (E mol %) is 20≦E<55. An ethylene vinyl alcohol-based polymer having a saponification degree of 98% or more is used as the first component, another thermoplastic polymer is used as the second component, and the composition ratio of the first component and the second component is 20:
80-80: 20 v1 combinations. ? g Synthetic fiber 3
In a method for producing a nonwoven fabric by moist heat bonding a fiber web containing 0% or more, water is applied to the 1a fiber web in an amount of 30% or more of its weight, and then a heating element is brought into contact with both surfaces of the fiber web.
Ta2.17E + 46.5. T <〜1.9 E
+245 、7<2゜13E + 59.4の範囲にあ
る加熱温度(T’C)に加熱し、繊維問を湿熱接着する
ことを特徴とする湿熱接着不織布の製造方法である。Ta2.17E + 46.5. T<~1.9E
This is a method for producing a heat-and-moisture adhesive nonwoven fabric, which is characterized by heating to a heating temperature (T'C) in the range of +245, 7<2°13E + 59.4, and bonding fibers together with heat and humidity.
第1の発明の構成をもつ複合繊維は融点以下の温度でも
充分な水蒸気の存在下で膨潤ゲル化し他ルコールの成分
比によって変化するが、Ta2.17E +46.5で
あればウェブに含まれる水分の蒸気により短時間で接着
させることができる EVOH複合繊維は湿熱下できわ
めて接着性に富み金属にもよく接着し、温度が高すぎる
と加熱体へ粘着が著るしくなるので、 T < 2.1
3E + 59.4及びT<−1,9E+245 (
融点)の範囲内にあることが必要である。The composite fiber having the structure of the first invention swells and gels in the presence of sufficient water vapor even at temperatures below the melting point, and changes depending on the component ratio of other alcohols, but if Ta2.17E +46.5, the water content in the web EVOH composite fibers can be bonded in a short period of time using steam of T 1
3E + 59.4 and T<-1, 9E+245 (
melting point).
第1図のグラフにEVOH繊維の第1成分のエチレンモ
ル比(Eモル%)と不織布の湿熱接着温度(T℃)の関
係を示す、加熱温度は融点を超えない範囲で、しかも加
熱体に粘着しない範囲の温度である。すなわち、20≦
Eく55の範囲内では20≦E〈46のとき(2,13
E +59.4) ℃より低く、46≦Eく55のとき
(−1,9E+245 )℃(融点)より低い温度であ
る。またEVOH繊維を水分の存在下に膨潤させうる温
度は(1,17E+46.5) ’C以上で、グラフの
斜線部分が接着可能な温度範囲である。The graph in Figure 1 shows the relationship between the ethylene molar ratio (E mol%) of the first component of EVOH fiber and the wet heat adhesion temperature (T°C) of the nonwoven fabric. The temperature is within the range where it does not occur. That is, 20≦
Within the range of Eku55, when 20≦E<46 (2,13
When 46≦E55, the temperature is lower than (-1,9E+245)°C (melting point). The temperature at which EVOH fibers can swell in the presence of moisture is (1,17E+46.5)'C or higher, and the shaded area in the graph is the temperature range at which bonding is possible.
EVOH繊維は単に加熱され温度が上昇するだけでは膨
潤ゲル化させることはむずかしく繊維ウェブの両面が加
熱体により接触されていることが必要である。It is difficult to cause EVOH fibers to swell and gel simply by heating and increasing the temperature, so both sides of the fiber web must be in contact with a heating element.
加熱体はロール、平板、コンベア等であって。The heating body is a roll, flat plate, conveyor, etc.
繊維ウェブを両面から挟む形で加熱するが、その圧力は
]Og、/c7程度以上であればよい、加熱体ウェブ両
面共に加熱することがウェブの厚さ方向に均一に接着を
起こさせるが0片側のみの加熱で、もう一方の面は単に
支持体としての働きをするものであってもよい、いずれ
の方法をとるかは目的とする不織布の用途により選択す
ればよい。The fibrous web is heated by sandwiching it from both sides, and the pressure need only be about ]Og,/c7 or more.Heating both sides of the heating element will cause adhesion to occur uniformly in the thickness direction of the web. It is also possible to heat only one side while the other side simply functions as a support, and which method to use may be selected depending on the intended use of the nonwoven fabric.
第2.3図に本発明の加熱方法の一例を示す。Figure 2.3 shows an example of the heating method of the present invention.
第2図は熱ロール(1)により繊維ウェブ(2)を挟持
、加熱する方式で繊維ウェブ(2)は前もってスプレー
(3)により水分を与えられ、熱ロール(1)により前
記温度範囲に加熱され接着し不織布(4)となって巻き
取られる。Figure 2 shows a method in which a fibrous web (2) is held and heated by heat rolls (1). The fibrous web (2) is previously moistened by spraying (3) and then heated to the above temperature range by the heat rolls (1). The non-woven fabric (4) is bonded and rolled up.
第3図は熱シリンダ−(5)で加熱する方式である。1
a維ウエブ(2)はスプレー(3)により水分を与えら
れた後、熱シリンダ−(5)で予熱され、水分が30%
以上である閏に加圧ロール(6)で押さえられ、このと
きEVOH繊維が膨潤ゲル化し不織布(4)を形成して
巻き取られる。Fig. 3 shows a heating method using a heat cylinder (5). 1
The a-fiber web (2) is moistened by a spray (3) and then preheated by a heat cylinder (5) until the moisture content is 30%.
The EVOH fibers are pressed by a pressure roll (6) on the above-mentioned lever, and at this time, the EVOH fibers swell and gel, forming a nonwoven fabric (4), which is then wound up.
(発明の作用)
本発明の方法はEVOH繊維の内部に水分が吸収されて
いる必要はなく、その周囲に水分か付着している状態で
あればよい、このような状態にある繊維ウェブを上記の
方法で加熱体に挟持すれば瞬間的に発生する水蒸気は加
熱体により繊維ウェブ内に封じ込められ、EVOH繊維
を瞬時に膨潤ゲル化させ接着させることが本発明の大き
な特色である。(Operation of the invention) In the method of the present invention, it is not necessary that moisture be absorbed inside the EVOH fibers, but it is sufficient that moisture is attached to the surroundings of the EVOH fibers. A major feature of the present invention is that when the EVOH fibers are held between heating bodies using the method described above, the instantaneously generated water vapor is contained within the fiber web by the heating bodies, and the EVOH fibers are instantly swollen and gelled to be bonded.
本発明に用いるエチレンモル比20〜55%のEVOH
繊維は極めて親水性に富むから繊維ウェブに与えられた
水分を繊維の周囲に吸着させるので上記方法に良好に用
いられる。EVOH with an ethylene molar ratio of 20 to 55% used in the present invention
Since fibers are extremely hydrophilic, moisture imparted to the fiber web is adsorbed around the fibers, making them suitable for use in the above method.
(発明の効果)
本発明による不織布は融点よりも低い温度で湿熱接着に
より製造できるばかりでなく、得られた不織布も湿熱接
着が可能であり、その接着の相手となるものはポリエス
テル、ナイロンなどの合成繊維や綿、レーヨンなどの天
然繊維の織物、不織布であれば衣料品のアップリケ、芯
地等に使用できる。その他1紙、木材、金属にも少量の
水分で湿熱接着ができるから、建築用、自動車の内装材
、断熱材として使用できる。(Effects of the Invention) Not only can the nonwoven fabric of the present invention be produced by wet heat bonding at a temperature lower than the melting point, but the obtained nonwoven fabric can also be bonded with wet heat, and the bonding partner is polyester, nylon, etc. Woven and non-woven fabrics made of synthetic fibers, cotton, rayon, and other natural fibers can be used for appliqués, interlining, etc. of clothing. 1) Since it can be bonded to paper, wood, and metal with a small amount of moisture using moisture heat, it can be used for construction, automobile interior materials, and insulation materials.
また不織布の他の構成線維を適宜選択することによって
親水性、耐薬品性の良好な不繊布を得れば衛生材料、工
業用フィルター、電池セパレーターとしても有用である
。Furthermore, if a nonwoven fabric with good hydrophilicity and chemical resistance can be obtained by appropriately selecting other constituent fibers of the nonwoven fabric, it will be useful as sanitary materials, industrial filters, and battery separators.
また本発明による不繊布の強度は、繊維方向に吋し直角
方向の引張強力を裂断長で表すとほぼ0、5に■以上に
なり、上記いずれの用途にも充分に耐えうるちのである
。In addition, the strength of the nonwoven fabric according to the present invention is approximately 0.5 or more when the tensile strength in the direction perpendicular to the fiber direction is expressed as the breaking length, and it can withstand all of the above uses. .
尚、裂断長は巾50關の試料の引張強力(g)を目付(
g/♂)で除した値(km )をとった。In addition, the tearing length is calculated by calculating the tensile strength (g) of a sample with a width of 50 mm by weight (
The value (km) divided by g/m) was taken.
(実施例)
EVOHmllとしてエチレンモル比E=29゜38及
び47のEVOHを各々第1成分、ポリプロピレンを第
2成分とし、第1成分を鞘成分に。(Example) As EVOHml, EVOH with ethylene molar ratio E=29°38 and 47 was used as the first component, polypropylene was used as the second component, and the first component was used as the sheath component.
第2成分を芯成分として複合比50.150(重量比)
の鞘芯型複合繊維を紡糸温度240℃で紡糸し、120
〜130℃で屹然延伸し、親水性油剤中を通して機械捲
縮を付与したものを乾燥し、繊度2デニール、カット長
51111の3種類のエチレンモル比の異なるステーブ
ルを作り以下の各実施例に用いた。Composite ratio 50.150 (weight ratio) with the second component as the core component
Sheath-core composite fibers were spun at a spinning temperature of 240°C, and
Stretches with different ethylene molar ratios of 2 denier fineness and 51111 cut length were made by stretching at ~130°C, mechanically crimped through a hydrophilic oil, and drying. there was.
実施例−1
E=29.のEVO)I繊維100%からなる目f寸3
0 g / +n”のカードウェブを作り、サポート紙
上に固定して霧吹きを用いて30 g / m”の水を
噴霧した後直径165龍のフラット熱ロール間を押し圧
10 kg / cWa”、加工速度5m/winで2
回通して湿熱接着した。ロール温度は70℃から]O’
C毎に昇温させ、各温度毎に試料をとり繊維の方向に対
し直角方向の引張強力を測定し、裂断長を求めた0本発
明方法による加熱湿度範囲は80.4〜121.1℃で
ある。加熱温度と裂断長を表−1に示す。Example-1 E=29. EVO) Made of 100% I fiber, mesh f size 3
A card web of 0 g/+n" was made, fixed on a support paper, sprayed with 30 g/m" water using a sprayer, and then pressed between flat heated rolls with a diameter of 165 mm under a pressure of 10 kg/cWa" for processing. 2 at speed 5m/win
It was passed through and bonded with wet heat. Roll temperature starts from 70℃]O'
The heating humidity range according to the method of the present invention is 80.4 to 121.1. It is ℃. Table 1 shows the heating temperature and fracture length.
実施例−2
E=38のEVOH繊維を用いて、実施例1と同様の条
件で不織布を作った0本発明による加熱温度範囲は91
.0〜140.3℃である。各加熱温度と裂断長を表−
1に示す。Example 2 A nonwoven fabric was made using EVOH fibers with E=38 under the same conditions as in Example 1. The heating temperature range according to the present invention was 91
.. The temperature is 0 to 140.3°C. Table showing each heating temperature and fracture length.
Shown in 1.
実施例−3
E−47のEVOH繊維を用いて、実施例1と同様の条
件で不織布を作った0本発明による加熱温度範囲は10
1.5〜155.7℃である。各加熱温度と裂断長を表
−1に示す。Example 3 A nonwoven fabric was made using E-47 EVOH fiber under the same conditions as in Example 1. The heating temperature range according to the present invention was 10
The temperature is 1.5 to 155.7°C. Table 1 shows each heating temperature and fracture length.
表−1に示すように、実施例1では加熱温度80℃以下
のとき裂断長0.5−に至らず、不織布の用途によって
は不適当である。また130℃となるとロールにEVO
H繊維が粘着し満足な不織布が得られない。As shown in Table 1, in Example 1, the tearing length did not reach 0.5 when the heating temperature was 80° C. or lower, which was inappropriate depending on the use of the nonwoven fabric. Also, when the temperature reaches 130℃, EVO is added to the roll.
The H fibers stick to each other, making it impossible to obtain a satisfactory nonwoven fabric.
同様に実施例2では90℃以下のときに、実施例3では
100℃以下のときに各々裂断長が小さく不適当である
が、130℃でも共に良好に製造できる。Similarly, in Example 2, when the temperature is 90°C or lower, the fracture length is small and unsuitable when the temperature is 100°C or lower, but both can be produced satisfactorily at 130°C.
実施例−4
実施例1と同じ繊維ウェブを、加熱ロールを凹凸のある
直径165關のスポットボンディング熱ロールと直径1
65m−のフラット熱ロールを用いて押し圧20kg/
as/、両ロール間の間隔0.04龍にした他は実施例
1と同様にして不織布を作った。各加熱温度と裂断長を
表−2に示す。Example 4 The same fibrous web as in Example 1 was heated using a spot bonding heat roll with a diameter of 165 cm and a heated roll having a diameter of 165 mm.
Pressing force 20kg/using a 65m flat heat roll
A nonwoven fabric was produced in the same manner as in Example 1, except that the distance between the rolls was 0.04 mm. Table 2 shows each heating temperature and fracture length.
実施例−5
実施例2と同じ繊維ウェブを用いて、実施例4と同様に
して不織布を作った。各加熱温度と裂断長を表−2に示
す。Example 5 Using the same fiber web as in Example 2, a nonwoven fabric was made in the same manner as in Example 4. Table 2 shows each heating temperature and fracture length.
実施例−6
実施例3と同じ繊維ウェブを用いて、実施例4と同様に
して不織布を作った。各加熱温度と裂断長を表−2に示
す。Example 6 Using the same fiber web as in Example 3, a nonwoven fabric was made in the same manner as in Example 4. Table 2 shows each heating temperature and fracture length.
以下余白
実施例4.5.6共に各温度で湿熱接着しているが、実
施例6はEVOH繊維の湿熱接着性が低下するので、ス
ポットボンディング熱ロールにより接着点が少なくなる
と低温度域の裂断長が小さくなる。Below, margin Examples 4, 5, and 6 are both bonded with heat and humidity at various temperatures, but in Example 6, the moisture and heat adhesion of EVOH fibers decreases, so if the number of bonding points is reduced by the spot bonding hot roll, it will cause cracking in the low temperature range. The cross section becomes smaller.
実施例−7
実施例2において、水分量をl Og / m2にした
他は全く同様の条件で加熱温度も同様に10℃毎に変化
させて6種類の不織布を作った。これら不織布の裂断長
は実施例2に比較して約40%であったがおおむね使用
に耐えうるちのである。Example 7 Six types of nonwoven fabrics were made under the same conditions as in Example 2, except that the water content was changed to 1 Og/m2, and the heating temperature was similarly changed in 10°C increments. The tearing length of these nonwoven fabrics was about 40% of that of Example 2, but they were generally durable for use.
実施例−8
実施例1において繊維ウェブにレーヨン(2デニール、
55m5)を67%混綿したものを用いた他はすべて実
施例1と同様の条件で不織布をつくった。各加熱温度毎
の裂断長を表−3に示す。Example-8 In Example 1, rayon (2 denier,
A nonwoven fabric was produced under the same conditions as in Example 1 except that a 67% blend of 55m5) was used. Table 3 shows the fracture length for each heating temperature.
実施例−9
実施例1において繊維ウェブにポリエステル(2デニー
ル、51龍)を67%混綿したものを用いた他はすべて
実施例1と同様の条件で不織布を作った。各加熱温度毎
の裂断長を表−3に示す。Example 9 A nonwoven fabric was made under the same conditions as in Example 1 except that the fiber web was mixed with 67% polyester (2 denier, 51 dragon). Table 3 shows the fracture length for each heating temperature.
実施例8.9共にEVOH繊維は33%しか入っていな
いが、各加熱温度における不織布の強力は80℃の場合
を除いてすべて使用に耐えうるちのである。Although both Examples 8 and 9 contained only 33% of EVOH fibers, the strength of the nonwoven fabrics at each heating temperature was sufficient to withstand use at all temperatures except at 80°C.
第1図はEVOHI!&lのエチレンモル比(E%)と
不織布の湿熱接着温度(T’C)の関係を示すグラフで
ある。第2.3図は本発明の!!遣方法の実施態様を示
すフローチャートである。
以下図において、】、熱ロール 2、繊維ウェブ 3.
スプレー 4 不繊布 5.熱シリンダ−6,加圧ロー
ルFigure 1 is EVOHI! 1 is a graph showing the relationship between the ethylene molar ratio (E%) of &l and the wet heat bonding temperature (T'C) of a nonwoven fabric. Figure 2.3 shows the features of the present invention! ! 3 is a flowchart illustrating an embodiment of the sending method. In the following figures, ], heat roll 2, fiber web 3.
Spray 4 Nonwoven fabric 5. Heat cylinder 6, pressure roll
Claims (2)
ケン化度98%以上のエチレンビニルアルコール共重合
体を第1成分,他の熱可塑性重合体を第2成分とし,第
1成分と第2成分の構成比が20:80〜80:20の
割合である複合繊維を30%以上含む繊維ウェブからな
る湿熱接着不織布。(1) Ethylene molar ratio (E mol%) is 20≦E<55,
An ethylene vinyl alcohol copolymer with a saponification degree of 98% or more is the first component, another thermoplastic polymer is the second component, and the composition ratio of the first component and the second component is 20:80 to 80:20. A wet heat bonded nonwoven fabric comprising a fiber web containing 30% or more of composite fibers.
ケン化度98%以上のエチレンビニルアルコール共重合
体を第1成分,他の熱可塑性重合体を第2成分とし,第
1成分と第2成分の構成比が20:80〜80:20の
割合である複合繊維を30%以上含む繊維ウェブを湿熱
接着する不織布の製法において,該繊維ウェブにその重
量の30%以上の水分を付与した後,該繊維ウェブの両
面に接触する加熱体により,T≧1.17+46.5,
T<−1.9E+245,T<2.13E+59.4の
範囲内にある加熱温度(T℃)に加熱し繊維間を湿熱接
着することを特徴とする湿熱接着不織布の製造方法。(2) Ethylene molar ratio (E mol%) is 20≦E<55,
An ethylene vinyl alcohol copolymer with a saponification degree of 98% or more is the first component, another thermoplastic polymer is the second component, and the composition ratio of the first component and the second component is 20:80 to 80:20. In a method for producing a nonwoven fabric by wet heat bonding a fibrous web containing 30% or more of composite fibers, after adding moisture of 30% or more of its weight to the fibrous web, a heating element in contact with both surfaces of the fibrous web ≧1.17+46.5,
A method for producing a moisture-heat bonded nonwoven fabric, which comprises heating to a heating temperature (T° C.) within the range of T<-1.9E+245 and T<2.13E+59.4 to bond fibers with moisture and heat.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62071141A JPH0791761B2 (en) | 1987-03-24 | 1987-03-24 | Wet heat adhesive non-woven fabric and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62071141A JPH0791761B2 (en) | 1987-03-24 | 1987-03-24 | Wet heat adhesive non-woven fabric and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63235558A true JPS63235558A (en) | 1988-09-30 |
JPH0791761B2 JPH0791761B2 (en) | 1995-10-04 |
Family
ID=13452016
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62071141A Expired - Lifetime JPH0791761B2 (en) | 1987-03-24 | 1987-03-24 | Wet heat adhesive non-woven fabric and method for producing the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0791761B2 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03113015A (en) * | 1989-09-22 | 1991-05-14 | Kuraray Co Ltd | Production of conjugate yarn |
JPH03130415A (en) * | 1989-10-13 | 1991-06-04 | Daiwabou Kurieito Kk | Conjugate fiber and its production |
JP2002302863A (en) * | 2001-04-02 | 2002-10-18 | Kuraray Co Ltd | Fiber structure for paint tool and method of manufacturing |
US6508897B1 (en) * | 1999-10-15 | 2003-01-21 | Kuraray Co., Ltd. | Porous fibrous structure and process for producing the same |
JP2006214048A (en) * | 2005-02-04 | 2006-08-17 | Daiwabo Co Ltd | Fiber structural product and method for producing the same, and method for producing filler-stuck fiber |
WO2007116676A1 (en) | 2006-03-31 | 2007-10-18 | Kuraray Kuraflex Co., Ltd. | Molded object having nonwoven fibrous structure |
JP2008179920A (en) * | 2007-01-25 | 2008-08-07 | Kuraray Kuraflex Co Ltd | Smooth lightweight board material |
WO2008108295A1 (en) * | 2007-03-08 | 2008-09-12 | Kuraray Kuraflex Co., Ltd. | Nonwoven fabric |
WO2009028564A1 (en) | 2007-08-31 | 2009-03-05 | Kuraray Kuraflex Co., Ltd. | Base material for cushioning and use thereof |
JP2009084715A (en) * | 2007-09-27 | 2009-04-23 | Kuraray Kuraflex Co Ltd | Cushioning material and method for producing the same |
JP2009084717A (en) * | 2007-09-28 | 2009-04-23 | Kuraray Kuraflex Co Ltd | Plate-like nonwoven fiber structure, sheet-like hinge having the fiber structure, and article with the hinge |
JP2014033775A (en) * | 2012-08-08 | 2014-02-24 | Livedo Corporation | Auxiliary sheet |
JP2014189911A (en) * | 2013-03-26 | 2014-10-06 | Kuraray Co Ltd | Agglutination processing method for fabric |
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JP4565902B2 (en) * | 2004-06-18 | 2010-10-20 | ダイワボウホールディングス株式会社 | Fiber molded body and method for producing the same |
JP4907879B2 (en) * | 2005-02-04 | 2012-04-04 | ダイワボウホールディングス株式会社 | Filler fixing yarn and woven / knitted fabric |
JP4603898B2 (en) * | 2005-02-04 | 2010-12-22 | ダイワボウホールディングス株式会社 | Fiber structure, method for producing the same, and method for producing filler-fixed fibers |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5626008A (en) * | 1979-08-08 | 1981-03-13 | Kuraray Co Ltd | Conjugate fiber |
JPS5747961A (en) * | 1980-09-03 | 1982-03-19 | Unitika Ltd | Heat and press adhesion of long fiber nonwoven fabric |
JPS5766200A (en) * | 1980-10-03 | 1982-04-22 | Kuraray Co | Paper and production thereof |
JPS61132664A (en) * | 1984-11-27 | 1986-06-20 | 日本バイリーン株式会社 | Production of nonwoven fabric containing polyvinyl alcohol fiber |
-
1987
- 1987-03-24 JP JP62071141A patent/JPH0791761B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5626008A (en) * | 1979-08-08 | 1981-03-13 | Kuraray Co Ltd | Conjugate fiber |
JPS5747961A (en) * | 1980-09-03 | 1982-03-19 | Unitika Ltd | Heat and press adhesion of long fiber nonwoven fabric |
JPS5766200A (en) * | 1980-10-03 | 1982-04-22 | Kuraray Co | Paper and production thereof |
JPS61132664A (en) * | 1984-11-27 | 1986-06-20 | 日本バイリーン株式会社 | Production of nonwoven fabric containing polyvinyl alcohol fiber |
Cited By (21)
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---|---|---|---|---|
JPH03113015A (en) * | 1989-09-22 | 1991-05-14 | Kuraray Co Ltd | Production of conjugate yarn |
JPH03130415A (en) * | 1989-10-13 | 1991-06-04 | Daiwabou Kurieito Kk | Conjugate fiber and its production |
US6508897B1 (en) * | 1999-10-15 | 2003-01-21 | Kuraray Co., Ltd. | Porous fibrous structure and process for producing the same |
JP2002302863A (en) * | 2001-04-02 | 2002-10-18 | Kuraray Co Ltd | Fiber structure for paint tool and method of manufacturing |
JP2006214048A (en) * | 2005-02-04 | 2006-08-17 | Daiwabo Co Ltd | Fiber structural product and method for producing the same, and method for producing filler-stuck fiber |
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US9758925B2 (en) | 2006-03-31 | 2017-09-12 | Kuraray Co., Ltd. | Molded object having nonwoven fibrous structure |
JP2008179920A (en) * | 2007-01-25 | 2008-08-07 | Kuraray Kuraflex Co Ltd | Smooth lightweight board material |
JPWO2008108295A1 (en) * | 2007-03-08 | 2010-06-17 | クラレクラフレックス株式会社 | Non-woven |
WO2008108295A1 (en) * | 2007-03-08 | 2008-09-12 | Kuraray Kuraflex Co., Ltd. | Nonwoven fabric |
JP5180184B2 (en) * | 2007-03-08 | 2013-04-10 | 株式会社クラレ | Non-woven |
JP5399907B2 (en) * | 2007-08-31 | 2014-01-29 | 株式会社クラレ | Base material for cushioning material and use thereof |
CN101842528B (en) | 2007-08-31 | 2012-09-26 | 可乐丽股份有限公司 | Base material for cushioning and use thereof |
TWI412641B (en) * | 2007-08-31 | 2013-10-21 | Kuraray Co | Substrate for cushioning material, method for producing the same, and use thereof |
AU2008292450B2 (en) * | 2007-08-31 | 2014-11-06 | Kuraray Co., Ltd. | Base material for cushioning and use thereof |
US9200390B2 (en) | 2007-08-31 | 2015-12-01 | Kuraray Co., Ltd. | Buffer substrate and use thereof |
WO2009028564A1 (en) | 2007-08-31 | 2009-03-05 | Kuraray Kuraflex Co., Ltd. | Base material for cushioning and use thereof |
JP2009084715A (en) * | 2007-09-27 | 2009-04-23 | Kuraray Kuraflex Co Ltd | Cushioning material and method for producing the same |
JP2009084717A (en) * | 2007-09-28 | 2009-04-23 | Kuraray Kuraflex Co Ltd | Plate-like nonwoven fiber structure, sheet-like hinge having the fiber structure, and article with the hinge |
JP2014033775A (en) * | 2012-08-08 | 2014-02-24 | Livedo Corporation | Auxiliary sheet |
JP2014189911A (en) * | 2013-03-26 | 2014-10-06 | Kuraray Co Ltd | Agglutination processing method for fabric |
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