JPH0233321A - Polyester fiber - Google Patents
Polyester fiberInfo
- Publication number
- JPH0233321A JPH0233321A JP18308688A JP18308688A JPH0233321A JP H0233321 A JPH0233321 A JP H0233321A JP 18308688 A JP18308688 A JP 18308688A JP 18308688 A JP18308688 A JP 18308688A JP H0233321 A JPH0233321 A JP H0233321A
- Authority
- JP
- Japan
- Prior art keywords
- polyester
- whitening agent
- core
- sheath
- polyester 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
- 239000000835 fiber Substances 0.000 title claims abstract description 32
- 229920000728 polyester Polymers 0.000 title claims abstract description 29
- 229920000642 polymer Polymers 0.000 claims description 16
- 239000002131 composite material Substances 0.000 claims description 10
- 239000006081 fluorescent whitening agent Substances 0.000 claims description 5
- 230000003287 optical effect Effects 0.000 abstract description 18
- 230000002087 whitening effect Effects 0.000 abstract description 8
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- -1 polyethylene terephthalate Polymers 0.000 abstract description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 4
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 4
- 238000002074 melt spinning Methods 0.000 abstract description 2
- 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 abstract 1
- 238000009987 spinning Methods 0.000 abstract 1
- 238000002845 discoloration Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical group C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 150000001869 cobalt compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 230000005808 skin problem Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は白変の優れたポリエステル繊維に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to polyester fibers with excellent white discoloration.
従来、衛生材料に用いられるポリエステル繊維は、高い
白変が要求されろものの発給、ただれ、かぶれなど皮膚
障害の虞れから蛍光増白剤の使用が困難であり、したが
りてポリエステル繊維の製造時に、酸化チタンの添加量
を上げたり、青味づけのためコバルト化合物を微量添加
したり或いは重合触媒として酸化ゲルマニウムを使用す
る等により白変の向上が行なわれたが充分な効果を得る
ことができなかった。Conventionally, polyester fibers used for sanitary materials require high white discoloration, making it difficult to use optical brighteners due to the risk of skin problems such as staining, sores, and rashes. The white discoloration was improved by increasing the amount of titanium oxide added, adding a small amount of cobalt compound to give it a blue tint, or using germanium oxide as a polymerization catalyst, but no sufficient effect could be obtained. There wasn't.
〔発明力1解決しようとする昧題〕
本発明は芯鞘型構造の複°合繊維の芯部に蛍光増白剤を
含有−せしめても驚くべきことに白変向上効果が得られ
ることに依りたもので、ポリエステル重合体に蛍光増白
剤を添加して充分白変を向上し、しかも皮膚に対しても
安全なポリエステル繊維を提供することにある。[Inventive power 1: Problem to be solved] The present invention surprisingly shows that even when a fluorescent brightener is contained in the core of a composite fiber having a core-sheath type structure, an effect of improving whitening can be obtained. The object of the present invention is to provide a polyester fiber which sufficiently improves whitening by adding an optical brightener to a polyester polymer and is also safe to the skin.
本発明はポリエステル繊維が芯鞘凰構造の複合ポリエス
テル繊維であって、芯部を蛍光増白剤を含む重合体にて
構成したことを特徴とするポリエステル繊維にある。The present invention resides in a polyester fiber characterized in that the polyester fiber is a composite polyester fiber with a core-sheath structure, and the core portion is made of a polymer containing a fluorescent whitening agent.
第1図(イ)、(ロ)、(ハ)K本発明のポリエステル
繊維の例の断面図を示すが、1は芯部の蛍光、増白剤を
含有する重合体、2は鞘部の蛍光増白剤を含まない1合
体、3は中空部を示す。Figures 1 (a), (b), and (c) K show cross-sectional views of examples of polyester fibers of the present invention, in which 1 shows the polymer containing fluorescent and brightening agent in the core, and 2 shows the sheath part. 1 indicates a combination containing no optical brightener, and 3 indicates a hollow portion.
なお、本発明のポリエステル繊維の芯部は第1図印、(
ロ)、(ハ)に示すように単一の芯部のほか2以上の複
数の芯部であってもよい。又第2図は本発明の第1図(
ロ)の芯鞘型構造の複合ポリエステル繊維を製造するた
めに用いられる一例の複合紡糸口金装置の縦断面図であ
る。ここで、第2図(イ)の4は分配板、5は前板、6
はノズル板を示す。第2図(ロ)は前板吐出孔のx −
x’断面図、第2図(ハ)はノズル板吐出孔のY −Y
’断面図である。Note that the core of the polyester fiber of the present invention is marked in Figure 1, (
As shown in (b) and (c), instead of a single core, two or more cores may be used. Also, Fig. 2 is the same as Fig. 1 of the present invention (
FIG. 2 is a longitudinal cross-sectional view of an example of a composite spinneret device used for producing composite polyester fibers having a core-sheath type structure in (b). Here, 4 in FIG. 2 (a) is a distribution plate, 5 is a front plate, and 6
indicates the nozzle plate. Figure 2 (b) shows the x − of the front plate discharge hole.
x' cross-sectional view, Figure 2 (c) is Y-Y of the nozzle plate discharge hole
'This is a cross-sectional view.
本発明の複合ポリエステル繊維の製造は、芯部を構成す
る蛍光増白剤含有ポリエステル1合体、及び鞘部を構成
するポリエステル重合体をそれぞれ押出機により溶融し
たあと複合紡糸口金装置に供給し溶融紡糸することによ
り行われる。そのあとは常法に従い、空冷、油剤付与、
ローラーでの引取り、延伸、熱処理、或いは更に捲縮付
与が施され繊維とされる。The composite polyester fiber of the present invention is manufactured by melting the optical brightener-containing polyester 1 aggregate constituting the core and the polyester polymer constituting the sheath using an extruder, and then supplying the composite spinneret to a composite spinneret device for melt-spinning. It is done by doing. After that, follow the usual methods, air cooling, applying oil,
The fibers are taken up with rollers, stretched, heat treated, or further crimped to form fibers.
本発明のポリエステル繊維に用いられる重合体は50モ
ル%以上がエチレンテレフタレートの繰り返し単位から
構成されるポリエチレンテレ7クレートである。重合度
は相対粘度(メタクレゾール、25℃)で1.5〜1.
8の範囲が好ましい。The polymer used in the polyester fiber of the present invention is polyethylene tere-7crate, in which 50 mol% or more is composed of repeating units of ethylene terephthalate. The degree of polymerization is a relative viscosity (metacresol, 25°C) of 1.5 to 1.
A range of 8 is preferred.
重合体には50モル%を超えない範囲でブタンジオール
、ヘキサンジオール等の他のジオールやインクタル酸、
5−ナトリウムスルホインフタル酸郷の他のジカルボン
酸を共1合してありてもよい。Other diols such as butanediol and hexanediol, inctaric acid,
Other dicarboxylic acids of the 5-sodium sulfoiphthalic acid group may also be combined.
本発明のポリエステル繊維は芯鞘型構造をなすが、繊維
断面に占める芯部の比率は20〜80%であることが好
ましい。芯部が20%未満では蛍光増白剤を含有させた
効果が小さく、80製を超えると芯部の1合体が繊維表
面の一部に露出したりする。The polyester fiber of the present invention has a core-sheath type structure, and the ratio of the core portion to the cross section of the fiber is preferably 20 to 80%. If the core content is less than 20%, the effect of containing the optical brightener will be small, and if it exceeds 80%, one core part will be exposed on a part of the fiber surface.
本発明で芯部の重合体に含有させる蛍光増白剤は270
〜290℃の温度範囲で分解せずポリエステル重合体中
に溶融分散するものであれば特に制限はない。このよう
な蛍光増白剤としてはビス−ベンゾオキサゾール誘導体
、トリアゾールフェニルクマリン誘導体、ビスステリル
ビフエ二ル誘導体尋を挙げろことができる。In the present invention, the optical brightener contained in the core polymer is 270
There is no particular restriction as long as it does not decompose in the temperature range of ~290°C and can be melted and dispersed in the polyester polymer. Examples of such optical brighteners include bis-benzoxazole derivatives, triazole phenylcoumarin derivatives, and bissteryl biphenyl derivatives.
蛍光増白剤を芯部の重合体に含有させる方法は特に制限
はないが、蛍光増白剤を高濃度に含有するマスターバッ
チをあらかじめ作り【おき1合体と均一混合し溶融混練
してもよいし、或いは蛍光増白剤の粉末を重合体表面に
均一に付着させ溶融混練してもよい。更には蛍光増白剤
を溶融もしくは溶解し、−旦液状にして、しかるのち溶
融重合体中に注入し溶Fll混線してもよい。There are no particular restrictions on the method of incorporating the optical brightener into the core polymer, but a master batch containing a high concentration of the optical brightener may be prepared in advance and mixed uniformly with the 1-unit mixture and melt-kneaded. Alternatively, a powder of a fluorescent whitening agent may be uniformly adhered to the surface of the polymer and then melt-kneaded. Furthermore, the optical brightener may be melted or dissolved, turned into a liquid, and then injected into the molten polymer to mix the molten Fll.
芯部の重合体への蛍光増白剤の含有量は0.01〜0.
5重量%とすることが好ましく、0.01重量%未満で
は白皮向上の効果が得られず、又0.5重量%を超えて
も顕著な効果が期待できない。The content of optical brightener in the core polymer is 0.01 to 0.
The content is preferably 5% by weight; if it is less than 0.01% by weight, no effect of improving white skin can be obtained, and if it exceeds 0.5% by weight, no significant effect can be expected.
本発明のポリエステル繊維は芯部に蛍光増白剤を含有す
るKもかかわらず高い白変を有し、かつ皮膚に対し安全
なので衛生材料や肌着材料に好適なるものである。The polyester fiber of the present invention has a high white discoloration despite containing a fluorescent whitening agent in the core, and is safe to the skin, so it is suitable for sanitary materials and underwear materials.
以下、本発明を実施例により説明する。 The present invention will be explained below with reference to Examples.
実施例
芯部成分として蛍光増白削りューコビアーEGM(サン
ド社製)を111Li%含むポリエチレンテレフタレー
ト重合体(相対粘度1.63、メタクレゾール中250
℃)のマスターバッチと酸化チタンを0.50重量%含
むポリエチレンテレフタレート1合体(相対粘度1.5
8)とを重量比で1;19に均一にブレンドし芯部1合
体に対し蛍光増白剤をo、o5xii%を含むチップ並
びに鞘部成分として酸化チタンを0.50重量%含tr
ポリエチレンテレフタレート1合体(相対粘度1.63
)のチップを、それぞれ別異の押出機に供給し290℃
で溶融したあとギヤポンプで芯部/鞘部=1/1になる
ようにして第2図に示す複合紡糸口金装置に導き270
℃で複合紡糸した。Example A polyethylene terephthalate polymer (relative viscosity 1.63, 250
°C) masterbatch and polyethylene terephthalate 1 containing 0.50% by weight of titanium oxide (relative viscosity 1.5
8) are uniformly blended in a weight ratio of 1:19, and a chip containing O, O5 xii% of a fluorescent whitening agent and a sheath component containing 0.50% by weight of titanium oxide based on the combined core part and tr.
Polyethylene terephthalate 1 combination (relative viscosity 1.63
) chips were fed to different extruders and heated at 290°C.
After melting with a gear pump, the core/sheath ratio is 1/1 and the mixture is introduced into the composite spinneret device shown in FIG. 2 (270).
The composite was spun at ℃.
前板は吐出孔を0.5謳φ、前板とノズル板との隙間を
0.2 mとした。ノズル板の吐出孔は第2図(ハ)に
示す形状(W= 0.3m、l = 0.15m、R=
1.8罪)のものを用いた。The discharge hole of the front plate was 0.5 mm in diameter, and the gap between the front plate and the nozzle plate was 0.2 m. The discharge hole of the nozzle plate has the shape shown in Fig. 2 (c) (W = 0.3 m, l = 0.15 m, R =
1.8 sin) was used.
紡出した糸条は、常法に従い空冷し油剤を付与したあと
680 rx/分で引取り集束した。The spun yarn was air-cooled and oiled according to a conventional method, and then taken off and bundled at 680 rx/min.
このあと未延伸糸を4時間、25℃、65RH%の条件
下にコンディショニングしたあと延伸機を用い90m/
分で4.0倍に延伸し、引続き押込捲縮装置に導き捲縮
を付与し、しかるのち150℃で15分熱処理し、51
m+に切断した。このようにして得た繊維の糸質を第1
表に示した。After this, the undrawn yarn was conditioned for 4 hours at 25°C and 65RH%, and then a drawing machine was used to
Stretched 4.0 times in 1 minute, then passed through a push-crimping device to give crimps, and then heat-treated at 150°C for 15 minutes.
Cut to m+. The quality of the fiber obtained in this way was
Shown in the table.
得られた繊維は蛍光増白剤が繊維表面に存在しないにも
かかわらず高い白変を有し、その製造工程においての蛍
光増白剤の浸出も全く認められず断糸も極めて少なかっ
た。The obtained fibers had a high level of white discoloration despite the fact that no optical brightener was present on the fiber surface, no leaching of the optical brightener was observed during the manufacturing process, and there was very little yarn breakage.
なお、繊維の白変は日本気色社製測色計0PTICAL
5ENSORmodel Z−11を用いてX。In addition, the white discoloration of the fibers is measured using a colorimeter 0PTICAL manufactured by Nippon Kishokusha.
5 using ENSOR model Z-11.
Y、Z値を測定し下記の式により計算したY、I。Y and I were calculated by measuring the Y and Z values and using the following formula.
値(小さい程白変が高い)で表わした。It was expressed as a value (the smaller the value, the higher the white discoloration).
比較例
実施例において芯部重合体に蛍光増白剤のマスターバッ
チをブレンドしなかった以外は、実施例と同一条件で得
た繊維の糸質も第1表に示した。Comparative Example Table 1 also shows the yarn quality of fibers obtained under the same conditions as in Examples, except that the core polymer was not blended with the optical brightener masterbatch.
第 1 表Table 1
第1図(イ)、(ロ)、(ハ)は本発明の繊維の例の横
断面図、第2図(イ)、(ロ)、C→は本発明の繊維を
製造する紡糸口金装置の例の縦断面図及びその部分断面
図である。
1・・・芯部重合体
2・・・鞘部重合体
3・・・中空部
(イノ
孝71図
cロン
(ハ)
第2図
(イ)Figures 1 (a), (b), and (c) are cross-sectional views of examples of the fibers of the present invention, and Figures 2 (a), (b), and C→ are spinneret apparatuses for producing the fibers of the present invention. FIG. 2 is a longitudinal cross-sectional view and a partial cross-sectional view of an example of FIG. 1...Core polymer 2...Sheath polymer 3...Hollow part (Inotaka 71 Figure C) Figure 2 (A)
Claims (1)
であって、芯部を蛍光増白剤を含む重合体にて構成した
ことを特徴とするポリエステル繊維。A polyester fiber characterized in that the polyester fiber is a composite polyester fiber having a core-sheath type structure, and the core portion is made of a polymer containing a fluorescent whitening agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18308688A JPH0233321A (en) | 1988-07-22 | 1988-07-22 | Polyester fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18308688A JPH0233321A (en) | 1988-07-22 | 1988-07-22 | Polyester fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0233321A true JPH0233321A (en) | 1990-02-02 |
Family
ID=16129517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18308688A Pending JPH0233321A (en) | 1988-07-22 | 1988-07-22 | Polyester fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0233321A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7265170B2 (en) | 2002-09-30 | 2007-09-04 | Bayer Materialscience Ag | Polycarbonate or polyester carbonate containing optical brighteners |
-
1988
- 1988-07-22 JP JP18308688A patent/JPH0233321A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7265170B2 (en) | 2002-09-30 | 2007-09-04 | Bayer Materialscience Ag | Polycarbonate or polyester carbonate containing optical brighteners |
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