JPH0482949A - Nonwoven fabric and production thereof - Google Patents
Nonwoven fabric and production thereofInfo
- Publication number
- JPH0482949A JPH0482949A JP2188603A JP18860390A JPH0482949A JP H0482949 A JPH0482949 A JP H0482949A JP 2188603 A JP2188603 A JP 2188603A JP 18860390 A JP18860390 A JP 18860390A JP H0482949 A JPH0482949 A JP H0482949A
- Authority
- JP
- Japan
- Prior art keywords
- nonwoven fabric
- sheath
- water repellent
- core
- film
- 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
Links
- 239000004745 nonwoven fabric Substances 0.000 title claims abstract description 65
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 21
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 21
- 230000002940 repellent Effects 0.000 claims abstract description 18
- 239000005871 repellent Substances 0.000 claims abstract description 18
- -1 polyethylene Polymers 0.000 claims abstract description 13
- 239000002344 surface layer Substances 0.000 claims abstract description 13
- 238000002844 melting Methods 0.000 claims abstract description 8
- 230000008018 melting Effects 0.000 claims abstract description 8
- 239000004743 Polypropylene Substances 0.000 claims abstract description 7
- 229920001155 polypropylene Polymers 0.000 claims abstract description 7
- 239000004698 Polyethylene Substances 0.000 claims abstract description 6
- 229920000573 polyethylene Polymers 0.000 claims abstract description 6
- 239000002131 composite material Substances 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000002861 polymer material Substances 0.000 claims description 12
- 229920001296 polysiloxane Polymers 0.000 claims description 10
- 125000006850 spacer group Chemical group 0.000 claims description 9
- 239000001993 wax Substances 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920002545 silicone oil Polymers 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims 1
- 239000000835 fiber Substances 0.000 abstract description 18
- 230000035699 permeability Effects 0.000 abstract description 7
- 229920000728 polyester Polymers 0.000 abstract description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 abstract description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 abstract description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 abstract description 3
- 239000004793 Polystyrene Substances 0.000 abstract description 2
- 229920002223 polystyrene Polymers 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract 3
- 239000010410 layer Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 17
- 230000000704 physical effect Effects 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 229910003591 H2PtCl6.6H20 Inorganic materials 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
- 229920000297 Rayon Polymers 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Treatment Of Fiber Materials (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、優れた通気性とともに撥水性、防水性をも兼
ね備えた特殊な不織布に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a special nonwoven fabric that has excellent air permeability as well as water repellency and waterproof properties.
通気性を有し且つ、撥水性、防水性を有する不織布とし
ては合成繊維でできている乾式法又は湿式法の不織布が
多い。しかし、一般にこれらのものは通気性は充分であ
るが、撥水性、防水性については充分であるとは言い難
く、そのため各種の工夫がなされているのが現状である
。例えば、■不織布の繊維表面に撥水剤を塗布する方法
、■疎水性フィルムを不織布層に貼り合わせ、その後に
フィルムに微細な孔を機械的に開ける方法、■フィルム
層に溶剤可溶性物質を練り込み、これを溶出させてフィ
ルム層に孔を開ける方法、■不織布をそのまま熱圧着し
て繊維間を密にする方法、等が挙げられる。Nonwoven fabrics that are breathable, water repellent, and waterproof are often dry-processed or wet-processed nonwoven fabrics made of synthetic fibers. However, although these materials generally have sufficient air permeability, they cannot be said to have sufficient water repellency or waterproof properties, and for this reason, various improvements have been made at present. For example, ■A method of applying a water repellent to the fiber surface of a non-woven fabric, ■A method of laminating a hydrophobic film to a non-woven fabric layer and then mechanically punching fine holes in the film, ■A method of kneading a solvent-soluble substance into the film layer. Examples include a method in which holes are formed in the film layer by eluting the nonwoven fabric, and a method in which the nonwoven fabric is heat-pressed as it is to make the fibers denser.
しかし乍ら、■の方法では、塗布した撥水剤が脱落して
性能が低下したり、■や■の方法では、フィルム層の孔
開&ノは再現性も悪く、且つコスI−高になり経済的に
も有利とは言えない。また■の不織布を熱圧着する方法
は比較的、品質及び経済性の点で優れているが、不織布
の特有の風合が損なわれるばかりでなく、フィルム化に
より引張強度や引裂強度が低下するという問題がある。However, in the method (■), the applied water repellent agent falls off and the performance deteriorates, and in the methods (■) and (2), the reproducibility of openings in the film layer is poor, and the cost is high. It cannot be said that it is economically advantageous. In addition, the method (2) of thermocompression bonding nonwoven fabrics is relatively superior in terms of quality and economy, but it not only impairs the unique texture of nonwoven fabrics, but also reduces tensile strength and tear strength when formed into a film. There's a problem.
本発明者らは上記問題点を解決すべく鋭意研究の結果、
本発明に到達したものである。As a result of intensive research by the present inventors to solve the above problems,
This has led to the present invention.
即ち、本発明の第1は、鞘部が芯部より低い融点からな
る高分子物質からなり、該鞘部の高分子物質に撥水剤を
含有・Uしめた複合合成繊維からなる不織布の片面又は
両面の表層部を熱圧着してフィルム化し、多層構造とし
たことを特徴とする不織布を、
本発明の第2は、鞘部が芯部より低い融点からなる高分
子物質からなり、該鞘部の高分子物質に撥水剤を含有せ
しめた複合合成繊維からなる不織布の片面又は両面の表
層部を熱圧着によりフィルム化することを特徴とする不
織布の製造法をそれぞれ内容とするものである。That is, the first aspect of the present invention is that the sheath is made of a polymeric material having a lower melting point than the core, and one side of a nonwoven fabric is made of a composite synthetic fiber in which the polymeric material of the sheath contains a water repellent and is coated with U. Alternatively, a nonwoven fabric is characterized in that the surface layer portions of both sides are thermocompression bonded to form a film to form a multilayer structure. Each content includes a method for manufacturing a nonwoven fabric, which is characterized by forming a surface layer on one or both sides of a nonwoven fabric made of a composite synthetic fiber in which a water repellent is contained in a polymeric substance into a film by thermocompression bonding. .
本発明に用いられる複合合成繊維は、鞘部が芯部より低
い融点よりなる高分子物質からできている複合合成繊維
であり、具体的には鞘部にポリエチレン又はポリスチレ
ン、芯部にポリプロピレン、ポリエステル、ポリアミド
(ナイロン)、或いは鞘部ニポリプロピレン、又はナイ
ロン−6、芯部にポリエステル、又はナイロン−66等
の組合せが挙げられる。The composite synthetic fiber used in the present invention is a composite synthetic fiber in which the sheath part is made of a polymer material with a lower melting point than the core part, and specifically, the sheath part is made of polyethylene or polystyrene, and the core part is polypropylene or polyester. , polyamide (nylon), or combinations such as polypropylene or nylon-6 for the sheath and polyester or nylon-66 for the core.
鞘部の高分子物質に添加される撥水剤としては、接触角
が90°以上のものを言い、咳高分子物質に良く混和さ
れることが必要である。例えば、般にシリコーンオイル
と言われているジメチルポリシロキサンや変性シリコー
ン化合物、例えばジメチルポリシロキサンのメチル基を
長鎖のアルキル基で置換したアルキル変性シリコーン化
合物や、フッ素変性化合物、例えばエチレン−4−フツ
化エチレン共重合体や、フッ素シリコーン化合物、更に
は各種ワックス類、例えばポリエチレンの低分子量物(
平均分子量約1500〜約5000)、ポリプロピレン
の低分子量物(平均分子量約3000〜約10000)
、パラフィン類等が挙げられ、これらは単独又は2種以
上組み合わせて用いられる。変性シリコーン化合物は、
例えば特開昭63−3076号公報に記載されているも
のを好適に用いることができる。撥水剤は鞘部の高分子
物質に対して0.5〜20.0重量%添加される。0゜
5重量%未満では撥水性の効果が低く、また20゜0重
量%を越えると鞘部の高分子物質の紡糸性や物性を著し
く低下せしめ、また不織布を更に熱圧着させる際にも繊
維間の融着を妨げるので好ましくない。撥水剤と鞘部高
分子物質との相溶性も重要であって、紡糸性に悪影響し
ないような撥水剤を事前に選んでおく必要がある。The water repellent added to the polymer material of the sheath must have a contact angle of 90° or more, and must be well mixed with the cough polymer material. For example, dimethylpolysiloxane, which is generally referred to as silicone oil, modified silicone compounds, such as alkyl-modified silicone compounds in which the methyl group of dimethylpolysiloxane is substituted with a long-chain alkyl group, and fluorine-modified compounds, such as ethylene-4- Fluorinated ethylene copolymers, fluorosilicone compounds, and various waxes, such as low molecular weight polyethylene (
average molecular weight of about 1,500 to about 5,000), low molecular weight polypropylene (average molecular weight of about 3,000 to about 10,000)
, paraffins, etc., and these may be used alone or in combination of two or more. Modified silicone compounds are
For example, those described in JP-A-63-3076 can be suitably used. The water repellent is added in an amount of 0.5 to 20.0% by weight based on the polymer material of the sheath. If it is less than 0.5% by weight, the water repellency effect will be low, and if it exceeds 20.0% by weight, the spinnability and physical properties of the polymer material in the sheath will be significantly reduced, and the fibers will be damaged when the nonwoven fabric is further thermocompressed. This is not preferable because it hinders the fusion between the two. The compatibility between the water repellent and the sheath polymer material is also important, and it is necessary to select in advance a water repellent that will not adversely affect spinnability.
このように鞘部の高分子物質に撥水剤を練り込んでいる
ため、これら複合合成繊維は耐久性のある撥水効果を有
し、水洗や外力によりその効果が低下することはない。Since the water repellent agent is incorporated into the polymer material of the sheath, these composite synthetic fibers have a durable water repellent effect, and the effect is not reduced by washing with water or external force.
このような樹脂構成で複合合成繊維よりなる不織布を得
る方法は、通常の複合ノズルより複合合成繊維を紡出し
、短繊維物から梳綿機でカード・ウェッブを得てニード
ルパンチング方式或いはエアージェット方式によっても
よく、また複合ノズルより複合合成繊維を得る際に、ス
パンボンド方式で直接不織布にしてもよい。A method for obtaining a nonwoven fabric made of composite synthetic fibers with such a resin composition is to spin composite synthetic fibers using a normal composite nozzle, obtain a carded web from staple fibers using a carding machine, and use a needle punching method or an air jet method. Alternatively, when obtaining composite synthetic fibers from a composite nozzle, it may be directly made into a nonwoven fabric using a spunbond method.
このようにして得られた不織布の片面又は両面の表層部
を熱圧着してフィルム化するのであるが、これには熱プ
レス機又は熱ロールを用いるのが良い。例えば、両面フ
ィルム化の場合は不織布の表裏両面より加熱するのが良
く、片面フィルム化する場合はフィルム化する面の方の
みを片面加熱すれば良い。この時の加熱温度は鞘部の高
分子物質が溶融して、芯部の高分子物質が溶融しない温
度を選択するのが好ましい。従って鞘部と芯部に用いら
れている高分子物質の溶融温度差の大きいものほど加工
し易い。また、この時の加圧は加熱温度とも関係はある
が、加圧はプレス板の場合0.1〜10kg/aflが
好ましく、熱ロールの場合も0.1kg〜5 kg /
cmの線圧が好ましい。いずれの場合も圧力がこれら
の値より低いとフィルム化する際にフィルム化炭が出易
く、また圧力がこれらの値より高い場合、不織布全体が
フィルム化され易(、所望の物性が得られ難い。The surface layer portions of one or both surfaces of the nonwoven fabric thus obtained are thermocompressed to form a film, and it is preferable to use a hot press machine or a hot roll for this purpose. For example, in the case of forming a double-sided film, it is preferable to heat both the front and back sides of the nonwoven fabric, and in the case of forming a single-sided film, it is sufficient to heat only the side to be formed into a film. The heating temperature at this time is preferably selected to be a temperature at which the polymer material in the sheath portion is melted, but the polymer material in the core portion is not melted. Therefore, the larger the difference in melting temperature between the polymeric substances used in the sheath and core, the easier it is to process. The pressure applied at this time is also related to the heating temperature, but the pressure applied is preferably 0.1 to 10 kg/afl in the case of a press plate, and 0.1 kg to 5 kg/afl in the case of a heated roll.
A linear pressure of cm is preferred. In either case, if the pressure is lower than these values, film-formed carbon is likely to come out during film formation, and if the pressure is higher than these values, the entire nonwoven fabric is likely to become a film (and it is difficult to obtain the desired physical properties). .
このようにして片面或いは両面より熱圧着して不織布の
表層部をフィルム化させるのであるが、ここで言うフィ
ルム化とは、繊維間が熱融着して殆ど繊維形態を残さず
融着し、殆どフィルl、化している状態を指す。このフ
ィルム化は温度、圧力、時間により、その状態をコント
ロールすることができる。本発明においては、鞘部、芯
部の樹脂、不織布の厚み等により上記の中から最適条件
を選び、フィルム化した表層部が不織布全体の厚みの1
/2以下からなる多層構造とすることが好ましい。フィ
ルム化した表層部と内部に繊維形態を残した不織布層と
からなる多層構造とすることにより、これらシート状物
の強度を保持し、且つ弾性、風合を保持させることがで
きる。何故なら、不織布全体をフィルム化すると繊維形
態が全く無くなり、繊維が有していた強度が著しく低下
すると共に、他方、繊維の絡み合いで有していた三次元
構造による不織布の弾性、風合も無くなるからである。In this way, the surface layer of the nonwoven fabric is formed into a film by thermocompression bonding from one or both sides, and film formation here means that the fibers are thermally fused together, leaving almost no fiber form behind. Refers to a state in which most of the fill is formed. The state of this film formation can be controlled by temperature, pressure, and time. In the present invention, the optimal conditions are selected from the above according to the resin of the sheath and core, the thickness of the nonwoven fabric, etc.
It is preferable to have a multilayer structure consisting of /2 or less. By forming a multilayer structure consisting of a filmed surface layer and a nonwoven fabric layer in which fibers remain inside, it is possible to maintain the strength, elasticity, and texture of these sheet-like materials. This is because when the entire nonwoven fabric is made into a film, the fiber morphology is completely lost, and the strength that the fibers had is significantly reduced, and on the other hand, the elasticity and texture of the nonwoven fabric due to the three-dimensional structure that it had due to the intertwining of the fibers are also lost. It is from.
この多層構造を有する不織布を作るに当たって、熱圧着
する際にスペーサーを用いると再現性よく且つ容易に目
的とするものが得られる。例えば全体の厚さを100μ
mとしたい場合は、約100μmのスペーサーを用いて
間隙を形成させた状態で熱圧着すればよく、これを熱ロ
ールで行う場合もロールに同様な間隙を与えて熱圧着す
ればよい。When making a nonwoven fabric having this multilayer structure, if a spacer is used during thermocompression bonding, the desired product can be easily obtained with good reproducibility. For example, the total thickness is 100μ
m, it is sufficient to use a spacer of about 100 μm to form a gap and perform thermocompression bonding, and when performing this using a hot roll, it is sufficient to provide a similar gap between the rolls and perform thermocompression bonding.
スペーサーとしては、熱圧着の時の熱により溶融しない
耐熱性を有する素材であれば特に制限されず、例えばス
テンレス等の金属、耐熱性樹脂等が挙げられる。The spacer is not particularly limited as long as it is made of a heat-resistant material that does not melt due to heat during thermocompression bonding, and examples thereof include metals such as stainless steel, heat-resistant resins, and the like.
このようにして得られた本発明の不織布は、フィルム化
された表層部により著しい澄水性及び防水性を有し、且
つ不織布表面層、即ち複合合成繊維の鞘部のみを融着さ
せ、芯部は繊維形態をそのまま保持しているため微孔を
有し、良好な通気性、透湿性をも兼ね備えたものである
。しかも繊維状の不織布層との複合体となっているため
、得られた不織布は強い引張強度、引裂強度、更に柔ら
かい風合をも有している。The nonwoven fabric of the present invention thus obtained has remarkable water clarity and waterproofness due to the filmed surface layer, and only the surface layer of the nonwoven fabric, that is, the sheath of the composite synthetic fiber is fused, and the core Because it maintains its fiber form, it has micropores and has good air permeability and moisture permeability. Moreover, since it is a composite with a fibrous nonwoven fabric layer, the obtained nonwoven fabric has strong tensile strength and tear strength, and also has a soft texture.
従って、本発明の不織布は、壁材や屋根材として用いら
れる通気性のある防水シートをはしめ、乾燥剤の包装材
、医療用のパッド材、オムツカバー等の衛生用材、或い
は表面が平滑であることから、タック上紙や伝票用紙等
記録材としても応用でき、しかもこれらを経済的に供給
することができる。Therefore, the nonwoven fabric of the present invention can be used as a material for wrapping breathable waterproof sheets used as wall materials or roofing materials, as packaging materials for desiccant materials, as sanitary materials such as medical pad materials, and diaper covers, or as materials with a smooth surface. Therefore, it can be applied as a recording material such as tack paper or slip paper, and moreover, these can be supplied economically.
以下、実施例及び比較例を挙げて本発明を更に詳しく説
明するが、これらにより本発明が限定されるものでない
。Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples, but the present invention is not limited by these.
合成例:撥水剤(変性シリコーン化合物)の合成ポリメ
チルハイドロジエンシロキサン(P−300、MW=2
2000) 45.6部、α−オレフィン(「ダイヤレ
ン−30」、三菱化成工業製、MW=650) 54.
4部、0.1%H2PtCl6・6H20テトラヒドロ
フラン溶液8部を反応器に仕込み、80’Cで8時間付
加反応させ、更に130°C]8時間反応させた。反応
生成物の粘度が約10000cpsに達した時反応を停
止させた。Synthesis example: Synthesis of water repellent (modified silicone compound) Polymethylhydrodiene siloxane (P-300, MW=2
2000) 45.6 parts, α-olefin (“Dialen-30”, manufactured by Mitsubishi Chemical Industries, Ltd., MW=650) 54.
4 parts of a 0.1% H2PtCl6.6H20 tetrahydrofuran solution were charged into a reactor, and the addition reaction was carried out at 80'C for 8 hours, and further reacted at 130°C for 8 hours. The reaction was stopped when the viscosity of the reaction product reached approximately 10,000 cps.
反応生成物はアセ1−ンで3回洗浄し、未反応部分を除
去し、精製乾燥した。得られた変性シリコーン化合物の
シリコーン含有率は45.6%であった。The reaction product was washed three times with acetone to remove unreacted parts, and purified and dried. The silicone content of the obtained modified silicone compound was 45.6%.
実施例1
高密度ポリエチレン(融点132’C)に、上記合成例
で得られた変性シリコーン化合物(五洋紙工■NR−B
)をポリエチレンに対し3重量%混合して鞘部の高分子
物質とし、芯部には結晶性ポリプロピレン(融点167
°C)を用い複合比を1/1として常法により単繊度3
デニールの複合合成繊維を得た。この複合合成繊維を繊
維長51mmにカットし、合成繊維用カードで製綿し、
120℃のエアージェットで予備圧着して、ウェッブ目
付40g/rrfの縦21.cmx横30cmの不織布
を得た。Example 1 The modified silicone compound obtained in the above synthesis example (Gonyo Paper Co., Ltd. NR-B) was added to high-density polyethylene (melting point 132'C).
) is mixed with polyethylene in an amount of 3% by weight to form the polymer material of the sheath, and the core is made of crystalline polypropylene (melting point: 167
°C) with a composite ratio of 1/1 and a single fineness of 3 using the usual method.
A denier composite synthetic fiber was obtained. This composite synthetic fiber was cut to a fiber length of 51 mm, and made into cotton using a synthetic fiber card.
Preliminary pressure bonding was performed using an air jet at 120°C, and the web weight was 40 g/rrf and the length was 21. A nonwoven fabric measuring cm x width 30 cm was obtained.
このウェッブを油圧式加熱プレス機で両面熱圧着した。This web was heat-pressed on both sides using a hydraulic heat press machine.
熱圧着方法はプレス板に厚さ150μmのスペーサーを
セットシ、次に上記ウェッブをセットして予熱を120
°Cで3分間行い、同一温度で本プレスを圧力5 kg
/ cfで3分間行い、厚さ180μmの不織布を得
た。この不織布の表裏両層のフィルム化層の厚さは、表
裏両層合ねセで80μmであった。The thermocompression bonding method is to set a spacer with a thickness of 150 μm on a press plate, then set the above web and preheat it to 120 μm.
°C for 3 minutes, and at the same temperature the main press was applied to a pressure of 5 kg.
/ cf for 3 minutes to obtain a nonwoven fabric with a thickness of 180 μm. The thickness of the film layers on both the front and back sides of this nonwoven fabric was 80 μm when both the front and back layers were combined.
得られた不織布の物性を第1表に示した。The physical properties of the obtained nonwoven fabric are shown in Table 1.
実施例2
スペーサーを用いない他は実施例1と同様にして、表裏
両層がフィルム化された全体の厚さ110μmの不織布
を得た。尚、フィルム化層の厚さは表裏両層合わせて5
0μmであった。Example 2 A nonwoven fabric having a total thickness of 110 μm and having both the front and back layers formed into films was obtained in the same manner as in Example 1 except that no spacer was used. In addition, the thickness of the film layer is 5 in total for both the front and back layers.
It was 0 μm.
得られた不織布の物性を第1表に示した。The physical properties of the obtained nonwoven fabric are shown in Table 1.
実施例3
実施例1の複合合成繊維を用い、実施例1と同様にして
目付70g/イのウェッブ状不織布を得た。このものを
油圧式加熱プレス機で加熱圧着させる際に、厚さ200
μmのスペーサーを用い、下側プレス板のみ120“C
に加熱して予熱を3分間行い、同一温度で本プレスを圧
力5 kg / cAで加熱圧着処理した。Example 3 Using the composite synthetic fiber of Example 1, a web-like nonwoven fabric with a basis weight of 70 g/I was obtained in the same manner as in Example 1. When this material is heat-pressed using a hydraulic heat press machine, the thickness is 200 mm.
Using a μm spacer, 120"C only for the lower press plate
Preheating was performed for 3 minutes, and at the same temperature, the press was heated and pressed at a pressure of 5 kg/cA.
このようにして得られたものは片側表面層のみがフィル
ム化し、該フィルム化層の厚さは30μmであり、他の
片面には繊維層が残り繊維の柔らかい風合を有した、全
体の厚さが480μmの不織布であった。The product obtained in this way has only one surface layer formed into a film, and the thickness of the filmed layer is 30 μm, and the other surface has a fiber layer remaining and has a soft texture, and has a total thickness of 30 μm. The nonwoven fabric had a length of 480 μm.
得られた不織布の物性を第1表に示した。The physical properties of the obtained nonwoven fabric are shown in Table 1.
比較例1
単繊度が3デニールで繊維長が51mmのポリプロピレ
ン繊維(三菱レーヨン製バイレン)を合成繊維用カード
で製綿し、140°Cのエアージェットで予備圧着して
ウェッブ目付40g/r+(の縦2Ic+nX横30c
+nの不織布を得ようとしたが、繊維間の接着の充分な
ものが得られなかった。また、エアージェットの温度を
更に160°Cに上げると繊維形態がくずれ、不織布が
得られなかった。Comparative Example 1 A polypropylene fiber (Mitsubishi Rayon's Vilene) with a single denier of 3 denier and a fiber length of 51 mm was produced using a synthetic fiber card, and was pre-pressed with an air jet at 140°C to give a web weight of 40 g/r+ (of Vertical 2Ic+nX Width 30c
Although an attempt was made to obtain a +n nonwoven fabric, sufficient adhesion between the fibers could not be obtained. Moreover, when the temperature of the air jet was further increased to 160° C., the fiber morphology collapsed and a nonwoven fabric could not be obtained.
比較例2
実施例1において、鞘部に変性シリコーン化合物を添加
しなかった他は実施例1と同様にして全体がフィルム化
された厚さ170μmの不織布を得た。この不織布の表
裏両層のフィルム化層の厚さは表裏両層合わせて80μ
mであった。Comparative Example 2 A nonwoven fabric having a thickness of 170 μm and having a thickness of 170 μm was obtained in the same manner as in Example 1 except that the modified silicone compound was not added to the sheath portion. The thickness of the film layer on both the front and back layers of this nonwoven fabric is 80μ in total.
It was m.
得られた不織布の物性を第1表に示した。The physical properties of the obtained nonwoven fabric are shown in Table 1.
実施例1と比較例1の比較から、複合合成繊維を用いな
い不織布では繊維間接着の不良な不織布しか得られない
ことがわかる。また実施例1と実施例2との比較から、
熱圧着する際にスペーサを用いることにより、フィルム
化層の厚さが容易にコントロール出来、特に引張強度、
引裂強度が大きい不織布が得られることが理解される。A comparison between Example 1 and Comparative Example 1 shows that a nonwoven fabric that does not use composite synthetic fibers can only provide a nonwoven fabric with poor interfiber adhesion. Also, from the comparison between Example 1 and Example 2,
By using a spacer during thermocompression bonding, the thickness of the film layer can be easily controlled, especially the tensile strength and
It is understood that a nonwoven fabric with high tear strength is obtained.
更に実施例1と比較例2とでは澄水性の評価を表ず接触
角θ及びΔθに大きな差が認められ、撥水剤を鞘部に併
用した効果が認められる。Furthermore, a large difference was observed in the contact angles θ and Δθ between Example 1 and Comparative Example 2 without evaluation of water clarity, and the effect of using the water repellent in combination with the sheath was observed.
実施例4
鞘部がポリエチレンにサンワックス15]−P(平均分
子量2000、三洋化成製)を10重量%混合したもの
からなり、芯部はポリエステルからなる複合比1/1の
複合合成繊維を常法のスパンポンド方式により紡出し、
同時に目付50g/ボの不織布を得た。このものを更に
油圧式加熱プレス機で実施例1と同様に」50μmのス
ペーサを用い、予熱を140°Cで3分間、同一温度で
本プレスを5 kg / ciで3分間行い、加熱圧着
処理して、厚さI 601t mの不織布を得た。この
不織布は表裏両層のフィルム化され、その厚みは表裏両
層合わせて70μmであった。物性を第2表に示した。Example 4 The sheath was made of polyethylene mixed with 10% by weight of Sunwax 15]-P (average molecular weight 2000, manufactured by Sanyo Kasei), and the core was made of polyester with a composite ratio of 1/1. Spun using the spunpond method according to the law,
At the same time, a nonwoven fabric with a basis weight of 50 g/bo was obtained. This material was further heat-pressed using a hydraulic heat press machine in the same manner as in Example 1, using a 50 μm spacer, preheating at 140°C for 3 minutes, and main pressing at the same temperature at 5 kg/ci for 3 minutes. As a result, a nonwoven fabric having a thickness of I 601t m was obtained. This nonwoven fabric was made into a film with both front and back layers, and the total thickness of both the front and back layers was 70 μm. The physical properties are shown in Table 2.
比較例3
実施例4において、鞘部に゛す゛ンワ・ノクス151P
を添加せず、また熱圧着時にスペーサーを用いなかった
他は、実施例4と同様にして厚ざ80μmのシート状物
を得た。このシート状物は全体が殆どフィルム化された
シート状物であった。物性を第2表に示した。Comparative Example 3 In Example 4, Suwanwa Nox 151P was added to the sheath part.
A sheet-like product with a thickness of 80 μm was obtained in the same manner as in Example 4, except that no . This sheet-like material was almost entirely formed into a film. The physical properties are shown in Table 2.
第
表
実施例4、比較例3とも通気性があり、且つ撥水性のあ
るものが得られているが、多層構造を有している実施例
3の方が通気性に優れ、また同じ目付にも拘らず引張強
度及び引裂強度が優れていた。また鞘部にワックスを混
合した実施例4が、より撥水性に優れていることがわか
る。Both Example 4 and Comparative Example 3 in Table 1 have air permeability and water repellency, but Example 3, which has a multilayer structure, has better air permeability and has the same basis weight. Despite this, the tensile strength and tear strength were excellent. Furthermore, it can be seen that Example 4, in which wax was mixed in the sheath portion, had better water repellency.
Claims (7)
り、該鞘部の高分子物質に撥水剤を含有せしめた複合合
成繊維からなる不織布の片面又は両面の表層部を熱圧着
してフィルム化し、多層構造としたことを特徴とする不
織布。1. The sheath is made of a polymer material with a lower melting point than the core, and the surface layer of one or both sides of a nonwoven fabric is made of a composite synthetic fiber in which the polymer material of the sheath contains a water repellent. A nonwoven fabric characterized by having a multilayer structure.
プロピレン又はポリエステル又はポリアミドである請求
項1記載の不織布。2. 2. The nonwoven fabric according to claim 1, wherein the sheath portion of the composite synthetic fiber is polyethylene, and the core portion is polypropylene, polyester, or polyamide.
織布全体の厚みの1/2以下である請求項1又は2記載
の不織布。3. The nonwoven fabric according to claim 1 or 2, wherein the surface layer portion formed into a film on one or both sides of the nonwoven fabric is 1/2 or less of the thickness of the entire nonwoven fabric.
、フッ素変性化合物、フッ素シリコーン化合物及びワッ
クス類から選択される少なくとも1種である請求項1乃
至3の各項記載の不織布。4. 4. The nonwoven fabric according to claim 1, wherein the water repellent is at least one selected from silicone oil, modified silicone compounds, fluorine modified compounds, fluorine silicone compounds, and waxes.
求項1乃至4の各項記載の不織布。5. The nonwoven fabric according to any one of claims 1 to 4, wherein the content of the water repellent is 0.5 to 20.0% by weight.
り、該鞘部の高分子物質に撥水剤を含有せしめた複合合
成繊維からなる不織布の片面又は両面の表層部を熱圧着
によりフィルム化することを特徴とする不織布の製造法
。6. The surface layer of one or both sides of a nonwoven fabric made of composite synthetic fibers, the sheath of which is made of a polymeric material with a lower melting point than the core, and the polymeric material of the sheath contains a water repellent, is formed into a film by thermocompression bonding. A method for producing a nonwoven fabric characterized by:
造法。7. 7. The manufacturing method according to claim 6, wherein the thermocompression bonding is performed using a spacer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2188603A JPH0482949A (en) | 1990-07-17 | 1990-07-17 | Nonwoven fabric and production thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2188603A JPH0482949A (en) | 1990-07-17 | 1990-07-17 | Nonwoven fabric and production thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0482949A true JPH0482949A (en) | 1992-03-16 |
Family
ID=16226560
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2188603A Pending JPH0482949A (en) | 1990-07-17 | 1990-07-17 | Nonwoven fabric and production thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0482949A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995026878A1 (en) * | 1994-04-05 | 1995-10-12 | Kimberly-Clark Corporation | Nonwoven fabric laminate with enhanced barrier properties |
US5688157A (en) * | 1994-04-05 | 1997-11-18 | Kimberly-Clark Worldwide, Inc. | Nonwoven fabric laminate with enhanced barrier properties |
JP2002249971A (en) * | 2001-02-27 | 2002-09-06 | Unitika Ltd | Sheet for reinforcing under-roof material |
JP2011225247A (en) * | 2010-04-20 | 2011-11-10 | Jx Nippon Anci Corp | Heat-sealing sheet, bag, and methods for manufacturing the sames |
EP2781637A4 (en) * | 2012-11-30 | 2015-09-30 | Lg Chemical Ltd | Nonwoven fabric formed from fiber coated with organic binder polymer compound, electrochemical device comprising nonwoven fabric, and method for manufacturing nonwoven fabric |
JP2017030218A (en) * | 2015-07-31 | 2017-02-09 | 三井化学株式会社 | Method for producing stretched film |
-
1990
- 1990-07-17 JP JP2188603A patent/JPH0482949A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995026878A1 (en) * | 1994-04-05 | 1995-10-12 | Kimberly-Clark Corporation | Nonwoven fabric laminate with enhanced barrier properties |
US5688157A (en) * | 1994-04-05 | 1997-11-18 | Kimberly-Clark Worldwide, Inc. | Nonwoven fabric laminate with enhanced barrier properties |
JP2002249971A (en) * | 2001-02-27 | 2002-09-06 | Unitika Ltd | Sheet for reinforcing under-roof material |
JP4618908B2 (en) * | 2001-02-27 | 2011-01-26 | ユニチカ株式会社 | Reinforcing sheet |
JP2011225247A (en) * | 2010-04-20 | 2011-11-10 | Jx Nippon Anci Corp | Heat-sealing sheet, bag, and methods for manufacturing the sames |
EP2781637A4 (en) * | 2012-11-30 | 2015-09-30 | Lg Chemical Ltd | Nonwoven fabric formed from fiber coated with organic binder polymer compound, electrochemical device comprising nonwoven fabric, and method for manufacturing nonwoven fabric |
US10153469B2 (en) | 2012-11-30 | 2018-12-11 | Lg Chem, Ltd. | Non-woven fabric made from fiber coated with organic binder polymer compound, electrochemical cell comprising the non-woven fabric, and method for making the non-woven fabric |
JP2017030218A (en) * | 2015-07-31 | 2017-02-09 | 三井化学株式会社 | Method for producing stretched film |
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