JPS6341549A - Hot-melt polyester based composition - Google Patents
Hot-melt polyester based compositionInfo
- Publication number
- JPS6341549A JPS6341549A JP18646986A JP18646986A JPS6341549A JP S6341549 A JPS6341549 A JP S6341549A JP 18646986 A JP18646986 A JP 18646986A JP 18646986 A JP18646986 A JP 18646986A JP S6341549 A JPS6341549 A JP S6341549A
- Authority
- JP
- Japan
- Prior art keywords
- polyester
- acid
- epoxy
- fibers
- 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.)
- Pending
Links
- 229920000728 polyester Polymers 0.000 title claims abstract description 40
- 239000000203 mixture Substances 0.000 title claims abstract description 17
- 239000012943 hotmelt Substances 0.000 title description 2
- 229920000098 polyolefin Polymers 0.000 claims abstract description 18
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 10
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 10
- 239000000835 fiber Substances 0.000 abstract description 51
- 238000002156 mixing Methods 0.000 abstract description 7
- 229920001634 Copolyester Polymers 0.000 abstract description 5
- 239000004593 Epoxy Substances 0.000 abstract description 5
- 239000002253 acid Substances 0.000 abstract description 5
- 230000001070 adhesive effect Effects 0.000 abstract description 4
- 239000011230 binding agent Substances 0.000 description 17
- -1 polyethylene Polymers 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 3
- 239000000306 component Substances 0.000 description 3
- 238000002074 melt spinning Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- LZFNKJKBRGFWDU-UHFFFAOYSA-N 3,6-dioxabicyclo[6.3.1]dodeca-1(12),8,10-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=CC1=C2 LZFNKJKBRGFWDU-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical group CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 101000802478 Sylvirana guentheri Brevinin-2GHa Proteins 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000013305 flexible fiber Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical group C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Manufacturing Of Multi-Layer Textile Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、ホットメルト型バインダー繊維の製造に適し
たポリエステル系組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a polyester composition suitable for producing hot-melt binder fibers.
(従来の技術)
近年、ふとん用中入れ綿やキルテイング用中入れ綿等の
繊維構造物において構成繊維相互間を接着する目的で、
ホントメルト型バインダー繊維が広く使用されるように
なってきた。(Prior art) In recent years, for the purpose of adhering constituent fibers in fiber structures such as padding cotton for futons and padding cotton for quilting,
True melt type binder fibers have come into wide use.
例えば、ポリエチレンを鞘とし、ポリプロピレンを芯と
する鞘芯型ポリオレフィン系バインダー繊維(特開昭5
8−180614号、同58−191215号等参照)
及び低軟化点共重合ポリエステルからなるバインダー繊
維や低軟化点共重合ポリエステルを鞘とし、高軟化点ポ
リエステルを芯とするポリエステル系バインダー繊維(
米国特許筒4,129,675号。For example, a sheath-core type polyolefin binder fiber with a polyethylene sheath and a polypropylene core (Japanese Patent Laid-Open No. 5
(See No. 8-180614, No. 58-191215, etc.)
and binder fibers made of low softening point copolyester or polyester binder fibers having a low softening point copolyester as a sheath and a high softening point polyester as the core.
U.S. Pat. No. 4,129,675.
特開昭57−66117号等参照)等がある。(See Japanese Patent Application Laid-Open No. 57-66117, etc.).
(発明が解決しようとする問題点)
上記のポリオレフィン系バインダー繊維は、繊維構造物
を構成する繊維(ベース繊維という)がポリオレフィン
系繊維の場合には、好ましいものであるが近年広く使用
されるようになってきたポリエステル繊維をベース繊維
とする場合には、接着効果が乏しいため、多量に使用し
なければならず。(Problems to be Solved by the Invention) The above polyolefin binder fibers are preferable when the fibers constituting the fiber structure (referred to as base fibers) are polyolefin fibers, but they have been widely used in recent years. When polyester fibers, which have become popular, are used as base fibers, they have to be used in large quantities because of their poor adhesive effect.
ベース繊維の特性を損なうという問題があった。There was a problem that the properties of the base fiber were impaired.
また、上記のポリエステル系バインダー繊維は。In addition, the above polyester binder fiber.
ベース繊維としてポリエステル繊維を使用する場合に良
好な接着効果を示すが、繊維を構成するポリエステルの
特性から、接着後の繊維構造物の風合が硬くなるという
問題があった。When polyester fibers are used as the base fibers, a good adhesive effect is exhibited, but there is a problem that the texture of the fibrous structure after bonding becomes hard due to the characteristics of the polyester constituting the fibers.
本発明は、このような従来のバインダー繊維の欠点を解
消し、特にポリエステル繊維をヘース繊維とする繊維構
造物の接着に適した。柔軟な繊維構造物を与えるポリエ
ステル系バインダー繊維を製造するのに適したポリエス
テル組成物を提供しようとするものである。The present invention eliminates such drawbacks of conventional binder fibers and is particularly suitable for adhering fiber structures using polyester fibers as heath fibers. It is an object of the present invention to provide a polyester composition suitable for producing a polyester binder fiber that provides a flexible fiber structure.
(問題点を解決するための手段)
本発明は2上記の目的を達成するもので、その要旨は、
軟化点100〜150℃の共重合ポリエステルA 25
〜75重量部、酸変性ポリオレフィン875〜25重量
部及びエポキシ変性アクリル樹脂C(AとBとの合計1
00重量部に対して)0〜50重量部からなるポリエス
テル系組成物にある。(Means for solving the problems) The present invention achieves the above two objects, and its gist is as follows:
Copolymerized polyester A with a softening point of 100 to 150°C 25
~75 parts by weight, 875 to 25 parts by weight of acid-modified polyolefin, and epoxy-modified acrylic resin C (total of A and B: 1
00 parts by weight) in a polyester composition consisting of 0 to 50 parts by weight.
本発明における共重合ポリエステルAとしては。As the copolymerized polyester A in the present invention.
ポリエステル繊維と良好な接着性を示すエチレンテレフ
タレート単位及びエチレンイソフタレート単位を主体と
する軟化点100〜150℃の共重合ポリエステルが好
ましく用いられる。A copolymerized polyester having a softening point of 100 to 150° C., which is mainly composed of ethylene terephthalate units and ethylene isophthalate units and exhibits good adhesion to polyester fibers, is preferably used.
また、酸変性ポリオレフィンBは、接着後の繊維構造物
にソフトな風合を与えるために配合されるもので、共重
合ポリエステルA25〜75重量部に対してで75〜2
5重量部の割合で配合される。共重合ポリエステルAの
割合が少なければポリエステル繊維との接着性が不十分
となり、酸変性ポリオレフィンBの割合が少なければ接
着後の繊維構造物の風合が硬くなる。In addition, acid-modified polyolefin B is blended to give a soft feel to the fiber structure after bonding, and is added in an amount of 75 to 2 parts by weight to 25 to 75 parts by weight of copolyester A.
It is blended in a proportion of 5 parts by weight. If the proportion of copolymerized polyester A is small, the adhesion with polyester fibers will be insufficient, and if the proportion of acid-modified polyolefin B is small, the texture of the fiber structure after adhesion will be hard.
酸変性ポリオレフィンBとしては、プロピレン。Acid-modified polyolefin B is propylene.
エチレン等のオレフィンとアクリル酸、メタクリル酸等
の脂肪族モノカルボン酸又はマレイン酸。Olefins such as ethylene and aliphatic monocarboxylic acids such as acrylic acid and methacrylic acid or maleic acid.
フマール酸等の脂肪族ジカルボン酸との共重合体が挙げ
られる。そして、酸変性の目的は、共重合ポリエステル
Aとの相溶性を高めるで紡糸性を向上させることにあり
、酸変性度は、酸価が30〜300g e q/106
gとなる程度が好ましい。酸価が低すぎると相溶性向上
効果が十分でなく、高すぎると配合時又は紡糸時にゲル
化しやすくなり、好ましくない。Examples include copolymers with aliphatic dicarboxylic acids such as fumaric acid. The purpose of acid modification is to improve spinnability by increasing compatibility with copolymerized polyester A, and the degree of acid modification is such that the acid value is 30 to 300 g eq/106
It is preferable to have a value of g. If the acid value is too low, the effect of improving compatibility will not be sufficient, and if it is too high, gelation will occur easily during blending or spinning, which is not preferable.
また、エポキシ変性アクリル樹脂(ポリアクリレート又
はポリメタクリレート)Cは、共重合ポリエステルAと
酸変性ポリオレフィンBとの相溶性をさらに高めて紡糸
性を一層向上させるために配合されるもので2AとBと
の合計100重量部に対してO〜50重量部配合される
。この配合量が多すぎると共重合ポリエステルAの割合
が相対的に低下してポリエステル繊維との接着性が不十
分となるため、良好な紡糸性を示す範囲で少なくするこ
とが望ましい。単糸繊度の大きいバインダー繊維の紡糸
に供する場合は、これを配合しなくても比較的紡糸性が
良いので、この配合量を0もしくはきわめて少なくする
ことができ、紡糸性の悪くなる単糸繊度5d以下のよう
な細繊度のバインダー繊維の紡糸に供する場合は、この
配合量を比較的多くする必要がある。In addition, epoxy-modified acrylic resin (polyacrylate or polymethacrylate) C is blended to further improve the compatibility between copolymerized polyester A and acid-modified polyolefin B to further improve spinnability. O to 50 parts by weight are added to a total of 100 parts by weight. If this amount is too large, the proportion of copolymerized polyester A will be relatively reduced, resulting in insufficient adhesion to polyester fibers, so it is desirable to reduce the amount within a range that provides good spinnability. When using binder fibers with a large single filament fineness for spinning, the spinnability is relatively good even without this addition, so the blending amount can be reduced to 0 or extremely small, and the single filament fineness that causes poor spinnability can be reduced. In the case of spinning binder fibers with a fineness of 5 d or less, it is necessary to increase the blending amount comparatively.
エポキシ変性アクリル樹脂Cとしては、メチルアクリレ
ート、エチルアクリレートメチルメタクリレート、エチ
ルメタクリレート等のアクリレート又はメタクリレート
モノマーと少量のグリシジルアクリレート、グリシジル
メタクリレート等のエポキシ基を有するアクリレート又
はメタクリレートモノマーとの共重合体及びこれらの成
分にさらにスチレン、酢酸ビニル等の共重合成分を加え
た共重合体が挙げられる。そしてエポキシ変性度は、エ
ポキシ価が100〜1000 g e q /10’
gとなる程度が適当である。エポキシ価が低すぎると配
合量を多くしなければならず、高すぎると配合時又は紡
糸時にゲル化しやすくなり好ましくない。Examples of the epoxy-modified acrylic resin C include copolymers of acrylate or methacrylate monomers such as methyl acrylate, ethyl acrylate, methyl methacrylate, and ethyl methacrylate with small amounts of acrylate or methacrylate monomers having epoxy groups such as glycidyl acrylate and glycidyl methacrylate; Examples include copolymers in which copolymer components such as styrene and vinyl acetate are added to the components. The degree of epoxy modification is such that the epoxy value is 100 to 1000 g eq /10'
An appropriate level is g. If the epoxy value is too low, the amount to be blended must be increased; if it is too high, gelation tends to occur during blending or spinning, which is undesirable.
共重合ポリエステルA、酸変性ポリオレフィンB及びエ
ポキシ変性アクリル樹脂Cの配合は、3者をミキサーで
トライブレンドして溶融紡糸に供する方法あるいはあら
かじめ溶融混練してブレンドポリマーチップとしておい
て溶融紡糸に供する方法等任意の手段により行うことが
できる。The copolymerized polyester A, the acid-modified polyolefin B, and the epoxy-modified acrylic resin C can be blended by tri-blending them in a mixer and subjecting them to melt-spinning, or by melt-kneading them in advance to form blended polymer chips and subjecting them to melt-spinning. This can be done by any means such as.
本発明のポリエステル系組成物は、バインダー繊維の接
着成分として適したものであり、この組成物のみからな
る単成分繊維としてもよいし、この組成物が繊維表面の
全部又は一部を形成している鞘芯型、サイドバイサイド
型、海島型等の複合繊維としてもよい。しかし、紡糸性
及び#i維動物性点で、鞘芯型複合繊維とするのが最も
好ましく。The polyester composition of the present invention is suitable as an adhesive component for binder fibers, and may be used as a monocomponent fiber consisting only of this composition, or as a fiber with this composition forming all or part of the fiber surface. It may also be a sheath-core type, side-by-side type, sea-island type, etc. composite fiber. However, in terms of spinnability and #i fiber property, it is most preferable to use a sheath-core type composite fiber.
その場合、芯成分としてポリエチレンテレフタレ−ト、
ポリブチレンテレフタレート及びこれらを主体とするポ
リエステルのようなポリエステルを用いるのが好ましく
、特に1強度特性の点でエチレンテレフタレート単位が
90モル%以上のポリエステルを用いるが好ましい。In that case, the core component is polyethylene terephthalate,
It is preferable to use polyesters such as polybutylene terephthalate and polyesters mainly composed of polybutylene terephthalate, and it is particularly preferable to use polyesters containing 90 mol % or more of ethylene terephthalate units in terms of one strength property.
(作 用)
本発明のポリエステル系組成物は、共重合ポリエステル
と相溶性を有する酸変性ポリオレフィンがポリエステル
と緊密に混合されるとともにエポキシ変性アクリル樹脂
のエポキシ基により共重合ポリエステルと酸変性ポリオ
レフィンとが一部架橋して混合の緊密さが高められるた
め、良好な紡糸性を示す。(Function) In the polyester composition of the present invention, the acid-modified polyolefin that is compatible with the copolymerized polyester is intimately mixed with the polyester, and the copolymerized polyester and the acid-modified polyolefin are bonded together by the epoxy group of the epoxy-modified acrylic resin. It exhibits good spinnability because it is partially crosslinked to increase the tightness of the mixture.
また、この組成物を用いたバインダー繊維は。Also, binder fibers using this composition.
組成物中の共重合ポリエステルがポリエステル繊維と良
好な接着性を有し、酸変性ポリオレフィンがソフトであ
るため、ソフトな風合を有する繊維構造物を与えるバイ
ンダー繊維となるのである。Since the copolymerized polyester in the composition has good adhesion to polyester fibers and the acid-modified polyolefin is soft, the binder fiber provides a fiber structure with a soft feel.
(実施例) 次に、実施例により本発明を具体的に説明する。(Example) Next, the present invention will be specifically explained with reference to Examples.
なお2例中の特性値等の測定法は5次のとおり。The method of measuring characteristic values, etc. in the two examples is as follows.
極限粘度
フェノールと四塩化エタンとの等重量混合物を溶媒とし
て、温度20°Cで測定。Intrinsic viscosity Measured at a temperature of 20°C using an equal weight mixture of phenol and tetrachloroethane as a solvent.
軟囮点 柳本自動融点測定装置AMP−1型を使用し。soft decoy point Yanagimoto automatic melting point measuring device AMP-1 type was used.
シリコーン浴中での針入温度を求めた。The needle insertion temperature in the silicone bath was determined.
勧
不織布を幅25nに裁断し、定速伸長型引張試験機で、
試料長1001m、引張速度1001m/分で測定。The non-woven fabric was cut to a width of 25n and tested using a constant speed extension type tensile tester.
Measured at a sample length of 1001 m and a tensile speed of 1001 m/min.
皿軟皮
JIS L 109645度カンチレバー法に準じて測
定。Measured according to the dish soft skin JIS L 109645 degree cantilever method.
爪金
10人のパネラ−による官能試験により1次の5段階で
評価。A sensory test conducted by 10 panelists was conducted on a five-point scale.
1:柔らかい、2:やや柔らかい、3:普通。1: Soft, 2: Slightly soft, 3: Average.
4:やや硬い、5:硬い。4: Slightly hard, 5: Hard.
実施例及び比較例
エチレンテレフタレート単位60モル%とエチレンイソ
フタレート単位40モル%とからなる共重合ポリエステ
ル(軟化点110℃、極限粘度0.626)。Examples and Comparative Examples A copolymer polyester consisting of 60 mol% of ethylene terephthalate units and 40 mol% of ethylene isophthalate units (softening point: 110°C, intrinsic viscosity: 0.626).
第1表に示したポリオレフィン及び変性アクリル樹脂を
第1表に示した割合で2軸スクリユ一型溶融混練機で、
240°Cで溶融混練し、ストランド状に吐出し、切断
してブレンドポリマーチップを得た。The polyolefins and modified acrylic resins shown in Table 1 were mixed in the proportions shown in Table 1 in a two-screw single-type melt-kneader.
The mixture was melt-kneaded at 240°C, discharged into strands, and cut to obtain blended polymer chips.
このブレンドポリマーチップとポリエチレンテレフタレ
ート (極限粘度0.633)チップとを減圧乾燥後1
通常の鞘芯型複合繊維用溶融紡糸装置を使用して、紡糸
孔数265の紡糸口金より、紡糸温度270℃、吐出量
347 g /分、複合比1:1で、前者が鞘となるよ
うに溶融紡糸し、冷却後、 1000m/分の速度で引
き取った。After drying this blended polymer chip and polyethylene terephthalate (intrinsic viscosity 0.633) chip under reduced pressure,
Using a normal sheath-core type composite fiber melt-spinning device, from a spinneret with 265 spinning holes, the spinning temperature was 270°C, the output rate was 347 g/min, and the composite ratio was 1:1, so that the former would become the sheath. After cooling, it was taken off at a speed of 1000 m/min.
得られた糸条を10万dのトウに集束し、延伸温度60
℃、延伸倍率3.1で延伸し、押し込み式クリンパ−で
捲縮を付与した後、長さ5111に切断して。The obtained yarn was bundled into a 100,000 d tow and stretched at a drawing temperature of 60
It was stretched at a stretching ratio of 3.1° C., crimped using a push-in crimper, and then cut into lengths of 5111 mm.
繊度4dのバインダー繊維を得た。Binder fibers with a fineness of 4d were obtained.
このバインダー繊維と繊度2d、長さ51龍のポリエチ
レンテレフタレート捲縮繊維とを40 : 60の割合
で混綿し、カードに通して40g/rtrの目付の一9
=
ウェブとし、140℃の回転乾燥機で1分間熱処理して
不織布を得た。This binder fiber and polyethylene terephthalate crimped fiber with a fineness of 2d and a length of 51 mm were mixed in a ratio of 40:60, and passed through a card to obtain a fiber with a basis weight of 40 g/rtr.
= A web was heat-treated for 1 minute in a rotary dryer at 140°C to obtain a nonwoven fabric.
得られた不織布の特性値等を第1表に示す。Table 1 shows the characteristic values of the obtained nonwoven fabric.
第1表において、ポリオレフィン■は、三菱油化社製マ
レイン酸共重合低密度ポリエチレン;三菱モディソクL
−400F(軟化点116℃)を示し、ポリオレフィン
@は、三菱油化社製低密度ポリエチレンホモポリマー;
三菱ノハティソクL−M420を示す。In Table 1, polyolefin ■ is maleic acid copolymerized low-density polyethylene manufactured by Mitsubishi Yuka Co., Ltd.; Mitsubishi Modisok L
-400F (softening point 116°C), and the polyolefin @ is a low-density polyethylene homopolymer manufactured by Mitsubishi Yuka;
Shows Mitsubishi Nohati Sok L-M420.
また、変性アクリル樹脂は、メチルメタクリレート59
モル%、スチレン38モル%及びグリシジルメタクリレ
ート3モル%からの共重合体で、平均分子量約30,0
00. xホキシ価300e q/106g(Dエポキ
シ変性ポリメタクリレート (軟化点120”c)を示
す。In addition, the modified acrylic resin is methyl methacrylate 59
mol%, copolymer of 38 mol% styrene and 3 mol% glycidyl methacrylate, average molecular weight approximately 30.0
00. x Phoxy value 300eq/106g (D Epoxy modified polymethacrylate (softening point 120''c).
なお、紡糸性は、8錘、5時間当たりの糸切れ回数を示
す。Note that spinnability indicates the number of yarn breakages per 5 hours using 8 spindles.
第1表
(発明の効果)
本発明によれば、ポリエステル繊維との接着性が良好で
、しかもソフトな繊維構造物を与えるポリエステル系バ
インダー繊維を良好な紡糸性のもとに製造することので
きるポリエステル系組成物が提供される。Table 1 (Effects of the Invention) According to the present invention, polyester binder fibers that have good adhesion to polyester fibers and provide soft fiber structures can be produced with good spinnability. A polyester-based composition is provided.
Claims (1)
25〜75重量部、酸変性ポリオレフィンB75〜25
重量部及びエポキシ変性アクリル樹脂C(AとBとの合
計100重量部に対して)0〜50重量部からなるポリ
エステル系組成物。(1) Copolymerized polyester A with a softening point of 100 to 150°C
25-75 parts by weight, acid-modified polyolefin B75-25
A polyester composition comprising 0 to 50 parts by weight of epoxy-modified acrylic resin C (based on 100 parts by weight in total of A and B).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18646986A JPS6341549A (en) | 1986-08-08 | 1986-08-08 | Hot-melt polyester based composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18646986A JPS6341549A (en) | 1986-08-08 | 1986-08-08 | Hot-melt polyester based composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6341549A true JPS6341549A (en) | 1988-02-22 |
Family
ID=16189016
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18646986A Pending JPS6341549A (en) | 1986-08-08 | 1986-08-08 | Hot-melt polyester based composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6341549A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008544001A (en) * | 2005-06-17 | 2008-12-04 | エボニック レーム ゲゼルシャフト ミット ベシュレンクテル ハフツング | Heat seal materials for aluminum sheets and polyethylene terephthalate sheets for polypropylene containers, polyvinyl chloride containers and polystyrene containers |
-
1986
- 1986-08-08 JP JP18646986A patent/JPS6341549A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008544001A (en) * | 2005-06-17 | 2008-12-04 | エボニック レーム ゲゼルシャフト ミット ベシュレンクテル ハフツング | Heat seal materials for aluminum sheets and polyethylene terephthalate sheets for polypropylene containers, polyvinyl chloride containers and polystyrene containers |
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