JPH0441732A - Composite fiber yarn of polyester fiber with wool - Google Patents
Composite fiber yarn of polyester fiber with woolInfo
- Publication number
- JPH0441732A JPH0441732A JP14507790A JP14507790A JPH0441732A JP H0441732 A JPH0441732 A JP H0441732A JP 14507790 A JP14507790 A JP 14507790A JP 14507790 A JP14507790 A JP 14507790A JP H0441732 A JPH0441732 A JP H0441732A
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- polyester
- wool
- shrinkage
- composite 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
- 239000000835 fiber Substances 0.000 title claims abstract description 116
- 229920000728 polyester Polymers 0.000 title claims abstract description 89
- 210000002268 wool Anatomy 0.000 title claims abstract description 58
- 239000002131 composite material Substances 0.000 title claims abstract description 47
- 238000009835 boiling Methods 0.000 claims abstract description 27
- 239000002202 Polyethylene glycol Substances 0.000 claims abstract description 21
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 abstract description 13
- 238000002156 mixing Methods 0.000 abstract description 9
- 238000004040 coloring Methods 0.000 abstract description 2
- 229920001634 Copolyester Polymers 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 34
- 238000004043 dyeing Methods 0.000 description 34
- 238000000034 method Methods 0.000 description 18
- 239000004744 fabric Substances 0.000 description 17
- 238000009987 spinning Methods 0.000 description 17
- 238000010438 heat treatment Methods 0.000 description 13
- 238000007334 copolymerization reaction Methods 0.000 description 12
- -1 aromatic dicarboxylic acids Chemical class 0.000 description 11
- 238000011161 development Methods 0.000 description 10
- 238000005406 washing Methods 0.000 description 8
- 239000000986 disperse dye Substances 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000009991 scouring Methods 0.000 description 6
- 239000000980 acid dye Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 238000007605 air drying Methods 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000009970 yarn dyeing Methods 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000007794 irritation Effects 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 206010022998 Irritability Diseases 0.000 description 1
- 101100078001 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) MSC2 gene Proteins 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000006085 branching agent Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229940011182 cobalt acetate Drugs 0.000 description 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- VVTXSHLLIKXMPY-UHFFFAOYSA-L disodium;2-sulfobenzene-1,3-dicarboxylate Chemical compound [Na+].[Na+].OS(=O)(=O)C1=C(C([O-])=O)C=CC=C1C([O-])=O VVTXSHLLIKXMPY-UHFFFAOYSA-L 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000009975 hank dyeing Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 238000009974 package dyeing Methods 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000009971 piece dyeing Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- IBBQVGDGTMTZRA-UHFFFAOYSA-N sodium;2-sulfobenzene-1,3-dicarboxylic acid Chemical compound [Na].OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O IBBQVGDGTMTZRA-UHFFFAOYSA-N 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、ポリエステルとウールの複合繊維糸に関する
。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a composite fiber yarn of polyester and wool.
本発明のかかる複合繊維糸は、織物、編物、装飾糸など
にされ、その特徴を生かして高級衣料用途に最適に用い
られるものである。The composite fiber yarn of the present invention can be made into woven fabrics, knitted fabrics, decorative yarns, etc., and can be optimally used for high-end clothing by taking advantage of its characteristics.
[従来の技術]
従来、ポリエステルフィラメントとウールとの複合繊維
糸は、コアヤーン、サイロフィル、カバーリングヤーン
として周知であり、ウールの風合、保温性にポリエステ
ルの高物性を兼備したポリエステル・ウールの高級な混
合糸である。特にウールのみ或いはポリエステル短繊維
等のスパン糸にくらべて、ケバが少なく糸に丸味があり
、ドレープ性のある風合から、細番手梳毛糸として注目
されている。[Prior Art] Conventionally, composite fiber yarns of polyester filaments and wool have been known as core yarn, silofil, and covering yarn. It is a high-quality mixed yarn. In particular, compared to spun yarns made only of wool or polyester short fibers, it is attracting attention as a fine count worsted yarn due to its less fluff, roundness, and drapeable texture.
しかしながら、ポリエステルは難染性がゆえに、ウール
と同条件で染色すると、色が淡くなり、ウールと色差が
生じ、イラツキと呼ばれる欠点となり、ウールとの同色
性は得られない。一方、通常のポリエステルの染色温度
である130〜135℃で染色すると、ウールとの同色
性は得られるが、ウールの風合が損なわれ、ガサガサし
た風合となる。また、ウールの貧化が大きく、強度、伸
度が大幅に低下する。従って、同色性とウールの風合、
強度などの兼ね合いから、110〜120’C程度の染
色温度で、キャリヤー等を併用し、妥協点を見い出しつ
つ、問題をかかえた状態で生産されているのが現状であ
る。However, because polyester is difficult to dye, if it is dyed under the same conditions as wool, the color will be lighter and there will be a color difference from wool, resulting in a defect called irritability, and it will not be possible to obtain the same color property as wool. On the other hand, when dyeing is carried out at 130 to 135° C., which is the normal dyeing temperature for polyester, the same color property as that of wool can be obtained, but the texture of the wool is impaired, resulting in a rough texture. In addition, the wool is greatly degraded, and its strength and elongation are significantly reduced. Therefore, the same color property and the texture of wool,
Due to the balance of strength and other factors, the dyeing temperature is currently about 110 to 120'C, and carriers and the like are used in combination, and while a compromise has been found, production is currently being carried out with problems.
一方、複合繊維糸用のポリエステルの収縮特性について
は、特に意を介さず使用されているのが現状である。ご
く低収縮糸を用いた場合には、ウールとの交絡が不十分
で、ウールからフィラメント糸が滑脱しやすくなったり
、製品に目ずれ欠点を生じたり、或いは高収縮糸を用い
た場合には緊締力が強く働き、風合が粗硬になるなどの
問題を惹起している。複合繊維糸の撚数についても、原
糸収縮との関連が十分把握できず、同様の問題があり、
場当り的に対応しているのが現状である。On the other hand, the shrinkage properties of polyester for composite fiber yarns are currently being used without much consideration. If very low shrinkage yarn is used, the intertwining with the wool will be insufficient, and the filament yarn will easily slip off from the wool, or the product will have misalignment defects, or if high shrinkage yarn is used, The tightening force is strong, causing problems such as the texture becoming rough and hard. There is a similar problem with regard to the number of twists of composite fiber yarns, as the relationship with yarn shrinkage cannot be fully understood.
Currently, we are responding on an ad hoc basis.
このような背景から、常圧染色でウールと同浴染色が可
能で、ウールの風合を損わないポリエステルフィラメン
ト複合繊維糸が望まれていた。Against this background, there has been a desire for a polyester filament composite fiber yarn that can be dyed in the same bath as wool using normal pressure dyeing and that does not impair the texture of wool.
かかる問題を解決せんがため、次のような常圧可染型ポ
リエステルが提案されている。In order to solve this problem, the following atmospheric pressure dyeable polyesters have been proposed.
ナトリウムスルホイソフタル酸を5モル%(8重量%)
以上共重合したカチオン染料可染型ポリエステルが、た
とえば、特開昭61−34022号、特開昭60−24
6847号、特開昭60−173185号、特開昭60
−88190号などにそれぞれ開示されている。5 mol% (8% by weight) of sodium sulfoisophthalate
The cationic dye-dyable polyester copolymerized above is disclosed in, for example, JP-A-61-34022 and JP-A-60-24.
No. 6847, JP-A-60-173185, JP-A-60
-88190, etc., respectively.
さらに、芳香族ジカルボン酸や脂肪族ジカルボン酸或い
は脂肪族ジオールを共重合させた易染性ポリエステル繊
維が、たとえば、特開昭51130320号、特開昭5
7−30169号などに開示されている。Furthermore, easily dyeable polyester fibers copolymerized with aromatic dicarboxylic acids, aliphatic dicarboxylic acids, or aliphatic diols are disclosed, for example, in JP-A-51130320 and JP-A-5.
No. 7-30169 and the like.
[発明が解決しようとする課題]
しかしながら、ナトリウムスルホイソフタル酸を共重合
したカチオン染料可染型ポリエステルは、染色性は高め
られるものの、糸強度が単繊維強度で2〜2.5g/d
と低いこと、収縮応力が2.5〜2.8g/dと小さく
、加工で十分な収縮が得られないこと、耐薬品性が乏し
く、カチオン染料の耐光堅牢度が乏しいなどの問題があ
る。[Problems to be Solved by the Invention] However, although the dyeability of cationic dyeable polyester copolymerized with sodium sulfoisophthalic acid is improved, the yarn strength is 2 to 2.5 g/d in terms of single fiber strength.
There are problems such as the shrinkage stress is as low as 2.5 to 2.8 g/d, insufficient shrinkage can be obtained during processing, the chemical resistance is poor, and the light fastness of cationic dyes is poor.
芳香族ジカルボン酸や脂肪族ジカルボン酸あるいは脂肪
族ジオールを共重合させた易染性ポリエステル繊維は、
常圧可染化に近づくものの、問題点も次のように多くな
る。Easy-to-dye polyester fibers copolymerized with aromatic dicarboxylic acids, aliphatic dicarboxylic acids, or aliphatic diols are
Although it is getting closer to becoming dyeable under normal pressure, there are many problems as follows.
例えば、アジピン酸、セバシン酸、アゼライン酸等の脂
肪族ジカルボン酸や脂肪族ジオールのうち、ブタンジオ
ール、ネオペンチルグリコール等を共重合したポリエス
テルや、イソフタル酸、1゜2−ビス(フェノキシ)エ
タン−4,4−ジカルボン酸等の芳香族ジカルボン酸を
共重合したポリエステル繊維では、常圧可染とするには
共重合率を15重量%以上とする必要があり、そのため
に、原糸強度の低下、耐光堅牢度の低下、原糸の貧化、
耐熱性の低下、製糸性不良等の問題があり、満足すべき
ものではなかった。For example, polyesters copolymerized with aliphatic dicarboxylic acids such as adipic acid, sebacic acid, and azelaic acid and aliphatic diols such as butanediol and neopentyl glycol, isophthalic acid, 1゜2-bis(phenoxy)ethane- For polyester fibers copolymerized with aromatic dicarboxylic acids such as 4,4-dicarboxylic acids, the copolymerization ratio must be 15% by weight or more to make them dyeable under normal pressure, which leads to a decrease in yarn strength. , decreased light fastness, poor yarn quality,
There were problems such as a decrease in heat resistance and poor spinning properties, and the results were not satisfactory.
本発明者らは、かかる従来技術における欠点に鑑み、ウ
ールに混用するポリエステルについて鋭意検討した結果
、特定の組成、収縮特性を有するポリエステルフィラメ
ント糸をウールに複合繊維することによって、同色性、
風合が大幅に改善できることを見いだし、本発明に到達
したものである。In view of the shortcomings in the prior art, the present inventors have made extensive studies on polyester to be mixed with wool. By incorporating polyester filament yarn having a specific composition and shrinkage characteristics into wool, the present inventors have found that the same color property,
The present invention was developed based on the discovery that the hand feel can be significantly improved.
即ち、本発明の目的は、発色性が高く、同色性に富み、
ウールのソフトな風合が生かされ、糸が滑脱しにく(、
均一で強力面でも問題ないポリエステルとウールの複合
繊維糸を提供することである。That is, the object of the present invention is to have high color development, high isochromism,
The soft texture of wool is utilized to prevent the thread from slipping (,
To provide a composite fiber yarn of polyester and wool that is uniform and has no problem in terms of strength.
[課題を解決するための手段]
本発明のポリエステルとウールの複合繊維糸は、前記の
目的を達成するために、次のいずれがの構成を有する。[Means for Solving the Problems] In order to achieve the above object, the polyester and wool composite fiber yarn of the present invention has any of the following configurations.
すなわち、
ポリエステルフィラメント糸とウールからなる複合繊維
糸であって、該ポリエステルが平均分子量500〜40
00のポリエチレングリコールを6.0〜10重量%共
重合した常圧可染性であり、単繊維強度が3.0〜6.
0g/d、沸騰水収縮率(以下、沸収)が3〜23%、
収縮応力が0.3〜0.9g/dであり、ウールを主体
とする短繊維とヨリ係数100〜220の範囲で加熱さ
れてなることを特徴とするポリエステルとウールの複合
繊維糸、または、
ポリエステルフィラメント糸とウールからなる複合繊維
糸であって、該ポリエステルが平均分子量500〜40
00のポリエチレングリコールを6.0〜10重量%共
重合した常圧可染性であり、且つ、該フィラメント糸が
低収縮糸と高収縮糸からなる混繊糸であり、ウールを主
体とする短繊維とヨリ係数100〜220の範囲で加熱
され、混繊糸の低収縮糸と高収縮糸の糸長差(以下、D
FL)が3〜20%であることを特徴とするポリエステ
ルとウールの複合繊維糸である。That is, it is a composite fiber yarn consisting of a polyester filament yarn and wool, and the polyester has an average molecular weight of 500 to 40.
00 polyethylene glycol copolymerized in an amount of 6.0 to 10% by weight, it is dyeable under normal pressure and has a single fiber strength of 3.0 to 6.0%.
0 g/d, boiling water shrinkage rate (hereinafter referred to as boiling yield) of 3 to 23%,
A composite fiber yarn of polyester and wool, which has a shrinkage stress of 0.3 to 0.9 g/d and is made by heating short fibers mainly made of wool and a twist coefficient in the range of 100 to 220, or Composite fiber yarn consisting of polyester filament yarn and wool, wherein the polyester has an average molecular weight of 500 to 40.
00 polyethylene glycol copolymerized in an amount of 6.0 to 10% by weight, it is dyeable under normal pressure, and the filament yarn is a mixed fiber yarn consisting of a low shrinkage yarn and a high shrinkage yarn, and is a short yarn mainly made of wool. The yarn length difference between low shrinkage yarn and high shrinkage yarn (hereinafter referred to as D
It is a composite fiber yarn of polyester and wool characterized by having a FL) of 3 to 20%.
なお、本発明においてDFLとは次の測定により求めら
れる値をいうものとする。Note that in the present invention, DFL refers to a value determined by the following measurement.
精練や染色などの熱処理を受けた複合繊維糸から20c
mの長さに切断して採取したポリエステルフィラメント
混繊糸を、目盛付きのガラス板上で、長さの異なる単繊
維別に分別する。単繊維のクリンプを除去するため、少
量のグリセリンをつけ、指でゆっくり伸ばしながら単繊
維の長さを測る。20c made from composite fiber yarn that has undergone heat treatment such as scouring and dyeing.
The polyester filament mixed fiber yarn was cut into lengths of m and collected, and then separated into single fibers of different lengths on a graduated glass plate. To remove crimps from the filaments, apply a small amount of glycerin and measure the length of the filaments while slowly stretching them with your fingers.
単繊維長の長い低収縮糸群の平均糸長11と単繊維長の
短い高収縮糸群の糸長12の差をDFLとする。The difference between the average yarn length 11 of the low shrinkage yarn group with long single fiber length and the yarn length 12 of the high shrinkage yarn group with short single fiber length is defined as DFL.
本発明に用いる常圧可染ポリエステルは平均分子量50
0〜4000のポリエチレングリコールを6.0〜10
重量%共重合したものである。The atmospheric pressure dyeable polyester used in the present invention has an average molecular weight of 50
0-4000 polyethylene glycol 6.0-10
It is copolymerized by weight%.
平均分子量が500未満の場合には、共重合時にポリエ
チレングリコールの一部が飛散し、共重合が一定化せず
、得られた糸の強伸度、収縮率、染色ムラ等を生じ、好
ましくない。一方、平均分子量が4000を越えるポリ
エチレングリコールを使用した場合には、共重合されな
い高分子量が増大するため、染色性の低下、耐光堅牢度
が低下し、好ましくない。If the average molecular weight is less than 500, a part of the polyethylene glycol will scatter during copolymerization, the copolymerization will not be constant, and the resulting yarn will have strong elongation, shrinkage, uneven dyeing, etc., which is not preferable. . On the other hand, when polyethylene glycol having an average molecular weight exceeding 4000 is used, the uncopolymerized high molecular weight increases, resulting in a decrease in dyeability and light fastness, which is not preferable.
また、ポリエチレングリコールの共重合率が6.0重量
%未満では、発色性が不十分であり、常圧可染性は得ら
れない。一方、10重量%を越える場合は、発色性は十
分であっても、原糸強度が低い、収縮が高すぎる、耐ア
ルカリ性等の物性が低下し、最終製品の品位が低下する
。Further, if the copolymerization rate of polyethylene glycol is less than 6.0% by weight, the color development is insufficient and normal pressure dyeability cannot be obtained. On the other hand, if it exceeds 10% by weight, even if the color development is sufficient, physical properties such as low fiber strength, too high shrinkage, and alkali resistance deteriorate, resulting in a decrease in the quality of the final product.
なお、ポリエチレングリコールをポリエステルに共重合
するため、通常のポリエステル繊維に比較して耐酸化分
解性が低下する傾向が有るため、これを改善するために
ポリエステル中に抗酸化剤を配合することが好ましく行
なわれる。In addition, since polyethylene glycol is copolymerized with polyester, there is a tendency for the oxidative decomposition resistance to be lower than that of ordinary polyester fibers, so it is preferable to incorporate an antioxidant into the polyester to improve this. It is done.
好ましい抗酸化剤としては、たとえば、フェノール系水
酸基の隣接位置に立体障害を有する置換基を持つフェノ
ール誘導体であるヒンダードフェノール系化合物をあげ
ることができる。Preferred antioxidants include, for example, hindered phenol compounds which are phenol derivatives having sterically hindered substituents adjacent to the phenolic hydroxyl group.
配合量は、ポリエステル繊維に対して0.05〜1.0
重量%が好ましい。The blending amount is 0.05 to 1.0 per polyester fiber.
Weight percent is preferred.
本発明に用いるフィラメントの素材であるポリエステル
には、必要に応じて他の共重合成分を共重合したり、他
のポリマをブレンドしても良い。The polyester that is the material of the filament used in the present invention may be copolymerized with other copolymer components or blended with other polymers, if necessary.
例えば、ペンタエリスリトール、トリメチロールプロパ
ン、トリメリット酸、ホウ酸等の鎖分岐剤を少割合共重
合したものであっても良い。For example, a small proportion of a chain branching agent such as pentaerythritol, trimethylolpropane, trimellitic acid, or boric acid may be copolymerized.
また、この他に任意の添加剤、例えば、酸化チタン等の
艶消し剤、紫外線吸収剤、難燃剤、顔料などを必要に応
じて含有させてもよい。In addition, arbitrary additives such as matting agents such as titanium oxide, ultraviolet absorbers, flame retardants, pigments, etc. may be included as necessary.
本発明に用いるフィラメントの素材であるポリエステル
は常圧可染性を示すものであるが、本発明では常圧可染
性を次のように定義するものとする。即ち、98℃染色
時の黒色明度L9gと130℃染色時の黒色明度L+3
0との差が1.0%以下の場合を常圧可染性とする。L
9BとLi2Oとの差が1.0%を越える場合には、1
30℃染色時の発色に対する98℃染色時の発色が不充
分であり、完全な常圧可染性は得られない。Polyester, which is the material of the filament used in the present invention, is dyeable under normal pressure, and in the present invention, dyeability under normal pressure is defined as follows. That is, black lightness L9g when dyed at 98°C and black lightness L+3 when dyed at 130°C.
A case where the difference from 0 is 1.0% or less is considered to be dyeable under normal pressure. L
If the difference between 9B and Li2O exceeds 1.0%, 1
The color development during dyeing at 98° C. is insufficient compared to the color development during dyeing at 30° C., and complete normal pressure dyeability cannot be obtained.
本発明において、L9B、Li2Oとは前記のとおり、
それぞれ98℃染色時の黒色明度、130°C染色時の
黒色明度であって、次の方法で測定した値をいう。In the present invention, L9B and Li2O are as described above,
The black brightness when dyeing at 98°C and the black brightness when dyeing at 130°C, respectively, are the values measured by the following method.
〈L、8、Li2Oの測定方法〉
ポリエステルフィラメントの繊維から靴下編地(−口筒
編地)を編成し、次いで精練剤としてサンデッ)C−2
9(三洋化成■製)を用い常法により98℃、20分間
煮沸下で、精練処理し、風乾後、これを弛緩状態で18
0℃、3分間乾熱セットした後に後述の条件で染色、水
洗、還元洗浄、水洗、風乾する。<Method for measuring L, 8, Li2O> A sock knitted fabric (-mouthpiece knitted fabric) is knitted from polyester filament fibers, and then sanded as a scouring agent) C-2
9 (manufactured by Sanyo Chemical Co., Ltd.) by a conventional method at 98°C under boiling for 20 minutes, and after air drying, it was heated to 18°C in a relaxed state.
After dry heat setting at 0° C. for 3 minutes, dyeing, washing with water, reduction washing, washing with water, and air drying are carried out under the conditions described below.
次いで、黒発色の明度を多光源分光測色計MSC2(ス
ガ試験機■製)にてL値(%)を測定する。Next, the lightness of the black color is measured as an L value (%) using a multi-light source spectrophotometer MSC2 (manufactured by Suga Test Instruments ■).
染色温度が98℃の場合の黒色明度(L値)をり、8、
染色温度が130℃の場合の黒色明度(L値)をL13
0とする。The black lightness (L value) when the dyeing temperature is 98°C is 8,
The black lightness (L value) when the dyeing temperature is 130°C is L13
Set to 0.
染色条件:
(イ)染料:Dianix Black BG−FS
200%品(三菱化成■製)
染色濃度ニア%ovr
染色助剤:ニッカサンソルト# 1200(日華化学工
業■製)
染色助剤濃度:0.5g/l
染色浴PH:6
染色浴比:1/30
(ロ)水洗
(ハ)還元洗浄
洗浄剤濃度
洗浄剤:ハイドロサルファイト 2g/l苛性ソーダ
2 g / IIサンデッドG−291,g
/l
(三洋化成■製)
洗浄温度1時間=80℃、20分
浴比:1/30
(ニ)水洗、風乾
本発明に用いるポリエステルフィラメントの単繊維強度
は3.0〜6.0g/dとするものである。単繊維強度
が3゜Og / d未満では製品物性や複合繊維の加工
時に糸切れなどの問題があり、実用性に乏しい。一方、
単繊維強度が6.0g/dを越えるポリエステル繊維を
得るのは一般に困難である。Staining conditions: (a) Dye: Dianix Black BG-FS
200% product (manufactured by Mitsubishi Kasei ■) Dyeing concentration near % ovr Dyeing aid: Nikka Sunsalt # 1200 (manufactured by NICCA Chemical ■) Dyeing aid concentration: 0.5 g/l Dyeing bath PH: 6 Dyeing bath ratio: 1/30 (B) Water washing (C) Reduction cleaning Cleaning agent concentration Cleaning agent: Hydrosulfite 2g/l caustic soda
2 g / II Sanded G-291, g
/l (manufactured by Sanyo Kasei ■) Washing temperature 1 hour = 80°C, 20 minutes Bath ratio: 1/30 (d) Washing with water, air drying The single fiber strength of the polyester filament used in the present invention is 3.0 to 6.0 g/d That is. If the single fiber strength is less than 3° Og/d, there will be problems such as product physical properties and thread breakage during processing of composite fibers, resulting in poor practicality. on the other hand,
It is generally difficult to obtain polyester fibers whose single fiber strength exceeds 6.0 g/d.
本発明の複合繊維糸において単一成分のポリエステルフ
ィラメントを用いる場合には、ポリエステルフィラメン
トの沸収を3〜23%、さらには6〜15%とするのが
好ましい。沸収が3%未満では収縮不足で、複合繊維糸
からポリエステルが滑脱しやすく、また、糸に締り感が
乏しくケバ立ちが発生する。一方、沸収が23%を超え
る場合は、糸の締り感が強すぎ、風合が粗硬化して好ま
しくない。When using a single component polyester filament in the composite fiber yarn of the present invention, it is preferable that the boiling yield of the polyester filament is 3 to 23%, more preferably 6 to 15%. If the boiling yield is less than 3%, there will be insufficient shrinkage, and the polyester will easily slip off from the composite fiber yarn, and the yarn will have a poor tightness and become fluffy. On the other hand, if the boiling yield exceeds 23%, the yarn will feel too tight and the texture will be rough and stiff, which is not preferable.
本発明の複合繊維糸においてポリエステルフィラメント
を低収縮糸と高収縮糸とからなる混繊糸とする場合には
、DFLを3〜20%、好ましくは、5〜15%とする
のが、後述する染色工程などの熱処理を受け、糸長差発
現による良好なふくらみ感を付与する観点から好ましい
。In the composite fiber yarn of the present invention, when the polyester filament is a mixed fiber yarn consisting of a low shrinkage yarn and a high shrinkage yarn, the DFL is set to 3 to 20%, preferably 5 to 15%, as described below. It is preferable from the viewpoint of imparting a good sense of fullness due to the development of yarn length differences when subjected to heat treatment such as a dyeing process.
DFLが3%未満では前記の向上効果が小さい。When DFL is less than 3%, the above-mentioned improvement effect is small.
一方、DFLが20%を越える場合は、低収縮糸側のル
ープが大きく発現し、糸が不均一になること、風合が硬
いなど好ましくない。On the other hand, if the DFL exceeds 20%, the loops on the low-shrinkage yarn side will be large, making the yarn non-uniform and having a hard texture, which is undesirable.
低収縮糸と高収縮糸の混繊率は、糸長差発現による良好
なふくらみ感を付与する観点からは1:1程度が好まし
い。The mixing ratio of low-shrinkage yarn and high-shrinkage yarn is preferably about 1:1 from the viewpoint of imparting a good fluffy feeling due to the difference in yarn length.
本発明においてフィラメントとして混繊糸を用いる場合
に、DFLを3〜20%とするための手段としては、精
練、染色等の沸水(95〜98℃)処理に併用して容易
に行ない得る。When a mixed fiber yarn is used as a filament in the present invention, the DFL can be easily adjusted to 3 to 20% by combining it with boiling water (95 to 98° C.) treatment such as scouring and dyeing.
例えば、複合繊維糸を製布したのち、連続糊抜精練や染
色と同時に実施することで得られる。糸染め(先染め)
の場合は、通常、バルキー発現処理を行なうスチーム処
理(90〜98℃)を適用することで得られる。後染め
、先染めともいずれも低張力下で実施することにより、
複合繊維糸の中のフィラメントを十分に弛緩収縮させる
のが好ましい。For example, it can be obtained by fabricating composite fiber yarn and then carrying out continuous desizing and dyeing at the same time. Yarn dyeing (yarn dyeing)
In this case, it is usually obtained by applying steam treatment (90 to 98° C.) which is a bulky treatment. By performing both piece dyeing and yarn dyeing under low tension,
It is preferred that the filaments in the composite fiber yarn are sufficiently relaxed and contracted.
本発明に用いるポリエステルフィラメントの収縮応力は
、0.3〜0.9g/dとするものである。0゜3 g
/ d未満の場合は、熱処理時にウールとの繊維間拘
束力や布帛組織拘束力に打ち勝てず、収縮不足となる。The shrinkage stress of the polyester filament used in the present invention is 0.3 to 0.9 g/d. 0゜3g
If it is less than /d, it will not be able to overcome the interfiber binding force with wool and the fabric structure binding force during heat treatment, resulting in insufficient shrinkage.
一方、0.9g/dを超えるポリエステル繊維を得るの
は一般に困難である。On the other hand, it is generally difficult to obtain polyester fibers exceeding 0.9 g/d.
なお、本発明の沸騰水収縮率、収縮応力、糸長差の測定
は次の方法で行なったものである。The boiling water shrinkage rate, shrinkage stress, and yarn length difference in the present invention were measured by the following methods.
〈沸騰水収縮率の測定〉
ポリエステルフィラメント糸を15■/dの荷重をかけ
て、測長する。(20)。<Measurement of boiling water shrinkage rate> A load of 15 cm/d was applied to the polyester filament yarn, and the length was measured. (20).
これを総状にし、ガーゼで包み98℃、20分間熱湯処
理する。次いで風乾し、処理前と同様の荷重で測長(l
+)L、次式で沸騰水収縮率Sを求める。Form this into a ball, wrap it in gauze, and heat it in boiling water at 98°C for 20 minutes. Next, it was air-dried, and the length was measured (l) with the same load as before treatment.
+)L, calculate the boiling water shrinkage rate S using the following formula.
S(%) = [(A’o Il+ ) /10 ]
X100く収縮応力の測定〉
ポリエステルフィラメント糸Loanを採取し、両端を
結んでループ状にする。これを、カネボウ■製熱収縮応
力測定器にて30■/dの荷重下、室温から200℃ま
で徐々に昇温しながら乾熱処理する。この時の最大収縮
応力(g)を読みとり、糸の総繊度(D)で除し、単繊
維繊度当りの収縮応力(■/d)を求める。S (%) = [(A'o Il+) /10]
Measurement of X100 Shrinkage Stress> Take a polyester filament yarn Loan and tie both ends to form a loop. This was subjected to dry heat treatment using a heat shrinkage stress measuring device manufactured by Kanebo ■ under a load of 30 ■/d while gradually increasing the temperature from room temperature to 200°C. The maximum shrinkage stress (g) at this time is read and divided by the total fineness of the yarn (D) to obtain the shrinkage stress per single fiber fineness (■/d).
なお、本発明に用いるポリエステルフィラメントの収縮
特性を制御する方法については特に限定するものではな
いが、前記組成のポリエステルを重合し、通常の紡糸速
度(1000〜1500m/分)で紡糸したのち、ポリ
エステルフィラメントを延伸するための熱処理温度を1
20〜190℃の範囲で容易に沸収を低くすることがで
きる。The method for controlling the shrinkage characteristics of the polyester filament used in the present invention is not particularly limited, but after polymerizing the polyester having the above composition and spinning it at a normal spinning speed (1000 to 1500 m/min), The heat treatment temperature for drawing the filament was set to 1
The boiling yield can be easily lowered in the range of 20 to 190°C.
なお、熱処理は熱板又は熱ピンで常法により施すことが
できる。Note that the heat treatment can be performed by a conventional method using a hot plate or a hot pin.
ポリエステルフィラメントを高収縮糸と低収縮糸の混繊
糸とする場合、高収縮糸を得る方法としては、前記熱処
理温度を100〜160℃に下げて延伸する方法や、紡
糸速度を2000〜4000m/分で製糸する方法、或
いは重合時に前記3成分からなる共重合組成の他に、イ
ソフタル酸やビスフェノール系のカルボン酸等の第4成
分を少量共重合する方法等があげられる。When polyester filament is made into a mixed fiber yarn of high shrinkage yarn and low shrinkage yarn, methods for obtaining high shrinkage yarn include a method of lowering the heat treatment temperature to 100 to 160°C and drawing, or a method of drawing at a spinning speed of 2000 to 4000 m/s. Examples include a method of spinning in minutes, or a method of copolymerizing a small amount of a fourth component such as isophthalic acid or bisphenol-based carboxylic acid in addition to the copolymer composition consisting of the three components during polymerization.
また、低収縮糸を得る方法としては、ポリエステルフィ
ラメント糸を仮ヨリ加工用熱処理機を用いて180〜2
20℃でさらに熱処理する方法や、紡糸速度を5000
〜7000m/分の範囲とする方法等があげられる。In addition, as a method for obtaining low shrinkage yarn, polyester filament yarn is heated to a temperature of 180 to 2
Further heat treatment at 20°C or spinning speed of 5000
Examples include a method in which the speed is within the range of ~7000 m/min.
混繊方法は高収縮糸と低収縮糸を空気交絡等で混繊する
方法や、紡糸と同時に混繊する同時紡糸混繊方法等が適
用できる。As the fiber blending method, a method of blending a high shrinkage yarn and a low shrinkage yarn by air entangling or the like, a simultaneous spinning and blending method of blending the fibers at the same time as spinning, etc. can be applied.
なお、本発明に用いるポリエステルフィラメント糸の形
態は、ケン縮のない延伸糸(生糸)またはケン縮の少な
いフィラメントを用いることが、かさがですぎて好まし
くない風合とならないようにする観点から好ましい。As for the form of the polyester filament yarn used in the present invention, it is preferable to use a drawn yarn without shrinkage (raw silk) or a filament with little shrinkage, from the viewpoint of avoiding undesirable texture due to excessive bulk. .
本発明に用いるポリエステルのフィラメントの繊度は特
に限定されるものではないが、20〜150Dのものを
ウールに複合繊維することが好ましい。例を挙げるなら
ば、120〜80番単糸の細番手複合繊維糸を得るには
、20〜30Dのポリエステルを、中番手の60〜48
番には30〜50D、太番手の36〜30番手には75
〜150Dのポリエステルを混用することが好ましい。Although the fineness of the polyester filaments used in the present invention is not particularly limited, it is preferable to use filaments of 20 to 150 D as conjugate fibers to wool. For example, in order to obtain a fine count conjugate fiber yarn with a single yarn count of 120 to 80, a polyester of 20 to 30D is mixed with a medium count of 60 to 48D.
30-50D for the number, 75 for the thick number 36-30
It is preferable to mix polyester of ~150D.
単繊維繊度は細番手用には0. 5〜2d、中番手用に
は2〜5dが好ましい。Single fiber fineness is 0.0 for fine count. 5 to 2 d, preferably 2 to 5 d for medium count.
本発明の複合繊維糸のヨリ係数は100〜220とする
ものである。ヨリ係数が100未満では滑脱しやすい、
すなわち、ウールがフィラメントから離脱してケバ立ち
やすい欠点があり、方、220を超えるものは、強い撚
のため硬い風合となる。The twist coefficient of the composite fiber yarn of the present invention is 100 to 220. If the twist coefficient is less than 100, it is easy to slip.
In other words, the wool tends to separate from the filaments and become fluffy, while those with a fiber count exceeding 220 have a hard texture due to the strong twist.
さらに、ヨリ係数100〜150のものはふくらみ感が
あり、秋冬用途に好適であり、ヨリ係数150〜220
の場合は適度のシャリ感を有するので、春夏用途に好適
である。Furthermore, those with a twist coefficient of 100 to 150 have a puffy feel and are suitable for autumn and winter applications, and those with a twist coefficient of 150 to 220
Since it has a moderate crispness, it is suitable for spring and summer applications.
なお、ヨリ係数は次式で求めた値である。Note that the twist coefficient is a value calculated using the following formula.
ヨリ係数=T/v’N
但し、T:ヨリ数(回/ m )、
N:メートル番手
本発明に用いる複合繊維用のウールは、ウール100%
とすれば、ウールの特徴を発揮できるので、特に好まし
いが、本発明の目的を達成しうる限りにおいて他の短繊
維を少量含有しても良い。Twist coefficient = T/v'N However, T: Number of twists (times/m), N: Metric count The wool for the composite fiber used in the present invention is 100% wool.
This is particularly preferable since it can exhibit the characteristics of wool, but small amounts of other short fibers may be included as long as the object of the present invention can be achieved.
この場合、本発明に用いるフィラメントの素材である常
圧可染ポリエステルからなる短繊維をウールに混紡した
ものは、ポリエステルの含有率か高まるので、寸法安定
性、ウォッシュ&ウェア性を向上させる効果があり好ま
しい。また、ウールに常圧カチオン染料可染性ポリエス
テル短繊維を混紡させる場合には、異色効果、抗ピル性
が発揮されるので好ましい。他の組合せとしては、ウー
ルにポリアクリル、ナイロン、綿等の常圧可染性短繊維
を混紡したものも好ましく使用できる。In this case, when short fibers made of pressure-dyable polyester, which is the material of the filaments used in the present invention, are blended with wool, the polyester content increases, so it has the effect of improving dimensional stability and wash and wear properties. Yes, it is preferable. In addition, it is preferable to blend wool with polyester short fibers dyeable with normal pressure cation dyes, as this provides a different color effect and anti-pilling properties. As another combination, a mixture of wool and pressure-dyable staple fibers such as polyacrylic, nylon, and cotton can also be preferably used.
また、本発明に用いるポリエステルフィラメントに、ナ
イロン、カチオン染料可染型ポリエステル、ポリエステ
ルホモポリマー等からなるフィラメントを少量混合する
ことにより、異色効果、杢染め効果が実現できる。Furthermore, by mixing a small amount of filament made of nylon, cationic dye-dyeable polyester, polyester homopolymer, etc. with the polyester filament used in the present invention, a unique color effect and heathered effect can be realized.
本発明に用いる複合繊維糸のポリエステルと短繊維の混
合比率は、特に限定するものではないが、フィラメント
を5〜50重量%、短繊維を95〜50重量%混合する
ことが好ましい。この場合、短繊維の比率をあげること
によって、風合効果が高められること、また、複合繊維
加工がしやすい等の利点がある。The mixing ratio of polyester and short fibers in the composite fiber yarn used in the present invention is not particularly limited, but it is preferable to mix 5 to 50% by weight of filaments and 95 to 50% by weight of short fibers. In this case, increasing the proportion of short fibers has the advantage of increasing the texture effect and making it easier to process composite fibers.
本発明に用いる複合繊維糸の形態の好ましい例を図によ
り説明する。A preferred example of the form of the composite fiber yarn used in the present invention will be explained with reference to the drawings.
第1図(a)は、シース・コアヤーンタイプの側面図で
あり、シース部がウールを主体とする短繊維2、コア部
が本発明に用いるポリエステルフィラメント1であ゛る
。第1図(b)は、断面図を示す。それぞれ複合して加
熱した後、染色熱を受けて、フィラメントが収縮したも
ののモデル図である。第1図のものは、コア部のポリエ
ステルの剛性、強度、高物性の機能性をもちながら、シ
ース部の短繊維のソフトな風合が最大限に発揮できる好
ましい形態である。FIG. 1(a) is a side view of a sheath/core yarn type, in which the sheath portion is short fibers 2 mainly made of wool, and the core portion is polyester filament 1 used in the present invention. FIG. 1(b) shows a cross-sectional view. It is a model diagram of filaments contracted by dyeing heat after being combined and heated. The one shown in FIG. 1 is a preferable form that can maximize the soft feel of the short fibers in the sheath part while having the rigidity, strength, and high physical properties of the polyester in the core part.
第2図は、サイロフィルタイブであり、フィラメントと
短繊維が均一に分散されている。フィラメントとウール
との交絡点が多くあるので、第1図のタイプにくらべて
糸の毛羽が少ないこと、糸に丸味があること、フィラメ
ントの光沢、清涼感が発揮できる特徴があるので好まし
い。FIG. 2 shows a silo filter ribbon in which filaments and staple fibers are uniformly dispersed. Since there are many intertwining points between the filament and the wool, it is preferable because the yarn has less fluff compared to the type shown in Figure 1, the yarn has a roundness, and the filament has a glossy and refreshing feel.
第3図は、カバーリングタイプであり、第2図のものに
くらべて分散性が小さい。フィラメントが表面に露出す
る機会が多いので、ポリエステルのシャリ感のある風合
が得られる。FIG. 3 shows a covering type, and its dispersibility is smaller than that in FIG. 2. Since there are many opportunities for the filaments to be exposed on the surface, a texture with the crisp feel of polyester can be obtained.
第4図は、シース・コアヤーンタイプであるが、フィラ
メントが低収縮糸と高収縮糸が混繊されてなるタイプで
ある。染色熱を受けて糸長差が発現し、コア部の高収縮
糸フィラメント1が最中6部に、低収縮フィラメント1
′がこの周りに交絡している。第1図のフィラメントが
単独糸であるのに対し、よりふくらみ感、ソフト感が増
長され、且つポリエステルの機能性を兼備する最も好ま
しい形態である。FIG. 4 shows a sheath/core yarn type in which the filaments are a mixture of low shrinkage yarn and high shrinkage yarn. Differences in yarn length occur due to the dyeing heat, with high shrinkage filament 1 in the core section being replaced by low shrinkage filament 1 in the middle 6 section.
' are intertwined around this. In contrast to the filament shown in FIG. 1, which is a single yarn, this is the most preferable form as it has a more fluffy and soft feel and also has the functionality of polyester.
なお、本発明の複合繊維糸の製造方法は、通常行なわれ
るように、短繊維の紡績時にフリースから供給された短
繊維にフィラメントを並列或いは重ね合せて、フロント
ローラーを経てスピンドルで合撚させて得られる。第1
図のシース・コアヤーンタイプは、短繊維を開繊状態に
しておき、この上にフィラメントを重ね合わせて合撚す
る方法で得ることができる。第2図のサイロフィルの場
合は、両側に短繊維を配置させ、中央にフィラメントを
配置し、合撚して得ることができる。第3図の場合は、
短繊維とフィラメントを並列に配置することにより得る
ことができる。In addition, the method for producing the composite fiber yarn of the present invention involves, as is usually done, filaments being arranged in parallel or superimposed on short fibers supplied from a fleece during spinning of short fibers, and then passed through a front roller and twisted by a spindle. can get. 1st
The sheath/core yarn type shown in the figure can be obtained by opening short fibers, overlapping filaments on top, and twisting them. In the case of the silofil shown in FIG. 2, short fibers are arranged on both sides, filaments are arranged in the center, and the fibers are twisted together. In the case of Figure 3,
It can be obtained by arranging short fibers and filaments in parallel.
染色は、分散染料と酸性染料を用い、常圧下、ノンキャ
リヤーで染色することができる。染色後は通常の方法で
ソーピングし、仕上げる。Dyeing can be carried out using disperse dyes and acid dyes under normal pressure and without a carrier. After dyeing, soap and finish using the usual method.
以下、本発明を実施例により、更に説明する。The present invention will be further explained below with reference to Examples.
[実施例」
なお、本実施例中の評価項目は次のようにして測定した
。[Example] The evaluation items in this example were measured as follows.
〈発色明度〉
複合繊維糸を分散染料と酸性染料で有彩色に染色し、染
色物の表面の明度を多光源分光測定計MSC−2型(ス
ガ試験機■製)にてL値(%)を測定する。L値が小さ
い程発色性が良好である。<Coloring brightness> Composite fiber threads are dyed in chromatic colors with disperse dyes and acid dyes, and the brightness of the surface of the dyed material is measured using a multi-light source spectrometer MSC-2 model (manufactured by Suga Test Instruments) to measure the L value (%). Measure. The smaller the L value, the better the color development.
〈同色性〉
ポリエステルと同浴で分散染料で染色し、更に酸性染料
で染色したウールの色相を等級比較判定した(5級二色
相が極めてよく似ておりイラツキがなく良好、4級:色
相がよく似ておりイラツキがなく良好、3級二色相がや
や似ており普通、2級二色相が似ているとは言えずイラ
ツキがあり悪い、1級:色相が全く似ずイラツキがあり
悪い)。<Same color> The hue of wool dyed with a disperse dye in the same bath as polyester and further dyed with an acid dye was graded and judged (grade 5: two hues are very similar and good with no irritation, grade 4: the hue is good). They are very similar and have no irritation and are good, 3rd grade two hues are somewhat similar and normal, 2nd grade two hues cannot be said to be similar and are irritating and bad, 1st grade: The hues are not similar at all and it is irritating and bad) .
く布帛の曲げ剛性〉
風合い測定器 KES−FB−2型(■KATOTEC
製)で測定した。Bending stiffness of fabric〉 Texture measuring instrument KES-FB-2 type (KATOTEC
(manufactured by).
〈布帛表面のマサツ係数〉
上記の曲げ剛性の測定と同様に風合い測定器KES−F
B−4型(■KATOTEC製)で測定した。<Masatsu coefficient of fabric surface> As in the measurement of bending rigidity above, the texture measuring instrument KES-F was used.
Measurement was carried out using Model B-4 (manufactured by KATOTEC).
〈布帛の風合評価〉
布帛を次の4段階に官能評価した。◎:ソフトでふくら
みがあり適度の張り、腰があるもの、○:これに準する
良好なもの、△:ソフト感、ふくらみに欠け、硬く劣る
もの、X:粗硬で劣るもの。<Evaluation of Texture of Fabric> The fabric was sensory evaluated on the following four levels. ◎: Soft and bulge, moderate tension, and firmness; ○: Comparably good quality; △: Soft feel, lacks bulge, and poor hardness; X: Poor roughness and hardness.
く布帛の折目摩擦強力〉
JIS L 1096^−3法(ユニバーサル刑法)に
よつた。Strong fold friction of fabric> Based on JIS L 1096^-3 law (Universal Penal Code).
〈複合繊維糸の滑脱性〉
染色した複合繊維糸をガイドのついたワインダーでコー
ン状に巻きとる工程を10回繰り返し行なう。巻きとり
時のガイドなどの抵抗で糸がしごかれ、フィラメント糸
からウール短繊維が滑脱する程度を、ウール短繊維のケ
バ立ち性を次の5段階で等級比較判定した。ケバ立ちが
最も少なく良好なもの(5級)、ケバ立ちが少なく良好
なもの(4級)、普通(3級)、ケバ立ちがあり、劣る
もの(2級)、著しくケバ立ちがあり、劣るもの(1級
)。<Sliding properties of composite fiber yarn> The process of winding the dyed composite fiber yarn into a cone shape using a winder with a guide was repeated 10 times. The degree to which the wool staple fibers slipped off the filament yarn when the yarn was strained by the resistance of the guide during winding, and the fluffiness of the wool staple fibers was graded in the following five grades. Good with the least amount of fluff (grade 5), Good with the least amount of fluff (grade 4), Average (grade 3), Poor with some fluff (grade 2), Poor with noticeable fluff. Things (grade 1).
く染色濃度〉
染色濃度(%0W1)は、分散染料の場合は対ポリエス
テルの重量比、酸性染料の場合はウールに対する重量比
である。Dyeing density> The dyeing density (%0W1) is the weight ratio to polyester in the case of a disperse dye, and the weight ratio to wool in the case of an acid dye.
総合評価は、◎:最も優れているもの、○:良好なもの
、△:若干問題あるもの、×:問題があるものの4段階
にそれぞれ評価した。The overall evaluation was in four stages: ◎: most excellent, ○: good, △: slightly problematic, and ×: problematic.
(実施例1)
〈常圧可染性ポリエステルの製造法〉
ジメチルテレフタレート100部、エチレングリコール
80部、抗酸化剤イルガノックス−1010(ケバ・ガ
イギー社製)0.3部、ジメチルポリシロキサン(東芝
シリコーン■製シリコーンオイル)0.01部、酢酸コ
バルト0.04部、三酸化アンチモン0.04部の混合
物を130℃〜230℃に加熱し、メタノールを抽出し
てエステル交換反応せしめた後、平均分子量1000の
ポリエチレングリコールを8.3部添加し、さらに23
0℃で30分間反応させた。その後、トリメチルホスフ
ェ−)0.03部を添加し、5分後に0.05部の二酸
化チタンを20重量%のエチレングリコールスラリーと
して添加し、低重合体を得た。得られた低重合体をさら
に230℃から280℃に徐々に昇温するとともに、大
気圧から1wHg以下の高真空まで徐々に減圧して重縮
合させ、極限粘度0.703、軟化点257℃の改質ポ
リエチレンテレフタレートを得た。(Example 1) <Production method of normal pressure dyeable polyester> 100 parts of dimethyl terephthalate, 80 parts of ethylene glycol, 0.3 part of antioxidant Irganox-1010 (manufactured by Keba Geigy), dimethylpolysiloxane (manufactured by Toshiba Co., Ltd.) A mixture of 0.01 part of silicone oil manufactured by Silicone ■, 0.04 part of cobalt acetate, and 0.04 part of antimony trioxide was heated to 130°C to 230°C, methanol was extracted, transesterification was carried out, and the average Add 8.3 parts of polyethylene glycol with a molecular weight of 1000, and then add 23 parts of polyethylene glycol with a molecular weight of 1000.
The reaction was carried out at 0°C for 30 minutes. Thereafter, 0.03 part of trimethyl phosphate was added, and after 5 minutes, 0.05 part of titanium dioxide was added as a 20% by weight ethylene glycol slurry to obtain a low polymer. The obtained low polymer was further heated gradually from 230°C to 280°C, and the pressure was gradually reduced from atmospheric pressure to a high vacuum of 1 wHg or less for polycondensation, resulting in a polymer with an intrinsic viscosity of 0.703 and a softening point of 257°C. Modified polyethylene terephthalate was obtained.
このようにして得られたポリエステル中の平均分子量1
000のポリエチレングリコールの共重合率は7.5倍
であった(実施例1■)。The average molecular weight in the polyester thus obtained is 1
The copolymerization rate of 000 polyethylene glycol was 7.5 times (Example 1■).
また、平均分子量1000のポリエチレングリコールを
それぞれ6.6部、11.0部添加した以外は上記とま
ったく同様に共重合して、平均分子量1000のポリエ
チレングリコールの共重合率が6.0重量%(実施例1
■)、10.0重量%(実施例1■)の共重合ポリエス
テルを得た。Further, copolymerization was carried out in exactly the same manner as above except that 6.6 parts and 11.0 parts of polyethylene glycol with an average molecular weight of 1000 were added, respectively, and the copolymerization rate of polyethylene glycol with an average molecular weight of 1000 was 6.0% by weight ( Example 1
■), 10.0% by weight (Example 1■) of copolymerized polyester was obtained.
得られたポリエステルチップを乾燥機内の雰囲気温度1
50℃で、lmmHg以下の減圧を維持して5時間乾燥
した。該乾燥チップを孔数24個の口金を用い、紡糸温
度290℃、紡糸速度1350m/+ainで紡糸した
。引続き、ホットローラー温度80℃、熱板温度165
°C1延伸倍率3.37倍、延伸速度800 m/mi
nで延伸し、50デニール、24フイラメント糸を得た
。The obtained polyester chips were placed in a dryer at an atmospheric temperature of 1
It was dried at 50° C. for 5 hours while maintaining a reduced pressure of 1 mmHg or less. The dried chips were spun using a nozzle with 24 holes at a spinning temperature of 290° C. and a spinning speed of 1350 m/+ain. Subsequently, the hot roller temperature was 80°C and the hot plate temperature was 165°C.
°C1 stretching ratio 3.37 times, stretching speed 800 m/mi
A 50 denier, 24 filament yarn was obtained.
得られた延伸糸(実施例1■)は単繊維強度5.1g/
d、伸度30%、沸収11−%、収縮応力0゜72 g
/ dの糸物性を有していた。また、延伸糸(実施例
1■)は単繊維強度5.2g/d、伸度31%、沸収1
0.5、収縮応力0.75g/d、延伸糸(実施例1■
)は単繊維強度4.8g / d、伸度34%、沸収1
1%、収縮応力0.71g/dであった。The obtained drawn yarn (Example 1■) had a single fiber strength of 5.1 g/
d, elongation 30%, boiling yield 11-%, shrinkage stress 0°72 g
The yarn had physical properties of /d. In addition, the drawn yarn (Example 1■) had a single fiber strength of 5.2 g/d, an elongation of 31%, and a boiling yield of 1
0.5, shrinkage stress 0.75 g/d, drawn yarn (Example 1■
) has a single fiber strength of 4.8 g/d, an elongation of 34%, and a boiling yield of 1
1%, and the shrinkage stress was 0.71 g/d.
このようにして得られたポリエステルフィラメント糸を
3本揃えて150Dにし、それぞれ24ゲージの靴下編
地を編成した。Three of the polyester filament yarns thus obtained were arranged to have a diameter of 150D, and each was knitted into a 24-gauge sock knitted fabric.
次いで常法により精練、セット、染色し、L98、LI
30を測定した結果を表1に示す。Next, scouring, setting, and dyeing are carried out by conventional methods to obtain L98, LI
The results of measuring 30 are shown in Table 1.
く複合繊維糸の染色布帛の製造法〉
前記ポリエステル延伸糸(50D)をそれぞれウール1
00%(138D相当)に精紡工程で第1図に示すよう
なシース・コアヤーンタイプに複合繊維した。複合繊維
はウールを開繊状にしておき、この上にポリエステル延
伸糸を重ねあわせ、フロントローラーを経て、スピンド
ルで撚係数180となるように撚をかけた。次いで、8
0℃。Method for producing dyed fabric of composite fiber yarn
00% (equivalent to 138D) was processed into a composite fiber in a sheath/core yarn type as shown in FIG. 1 in a spinning process. The composite fiber was made of wool that was spread, and a drawn polyester yarn was layered thereon, passed through a front roller, and twisted with a spindle to a twist coefficient of 180. Then 8
0℃.
30分スチーミングし、撚止めセットした。得られた複
合繊維糸は48番単糸、ポリエステル混率27重量%で
あった。Steamed for 30 minutes and set the twist. The obtained composite fiber yarn was a No. 48 single yarn and had a polyester blend ratio of 27% by weight.
次いで、該複合繊維糸をタテおよびヨコ糸に用いてそれ
ぞれ2/1の綾織物に製織した。Next, the composite fiber yarns were used as warp and weft yarns to weave a 2/1 twill fabric, respectively.
次いで、拡布状で連続リラックス精練(98℃。Next, continuous relaxing scouring (98°C) was carried out in the form of a spread cloth.
7分間)し、十分に収縮、熱処理した。7 minutes), and was sufficiently shrunk and heat treated.
次いで、洗絨、乾熱セット(160℃、40秒)し、前
記黒色の分散染料7%owfとウール用黒色酸性含金染
料KaYakalan Black BGL (日本
化薬■製)7%owfとを混合し、同98°C960分
の条件でキャリヤーを用いることなく染色してた。染色
後、ソーダ灰1g//、非イオン洗浄剤0. 5g /
/の弱アルカリ浴で70℃、20分ソーピング、水洗
し、仕上げた。織物は仕上幅154an。Next, the carpet was washed and set under dry heat (160° C., 40 seconds), and the black disperse dye 7% OWF and the black acidic metal-containing dye for wool KaYakalan Black BGL (manufactured by Nippon Kayaku ■) 7% OWF were mixed. It was dyed under the same conditions of 98°C and 960 minutes without using a carrier. After dyeing, soda ash 1g//, non-ionic detergent 0. 5g/
Finished by soaping in a weak alkaline bath at 70°C for 20 minutes and washing with water. The finished width of the fabric is 154an.
タテ密度102本/吋、ヨコ密度78本/吋であった。The vertical density was 102 lines/inch, and the horizontal density was 78 lines/inch.
結果を表1に示す。The results are shown in Table 1.
(比較例1〜3)
平均分子量1000のポリエチレングリコールの共重合
率を変えた以外、実施例1と全く同様にして重合、製糸
を行なった。(Comparative Examples 1 to 3) Polymerization and spinning were carried out in exactly the same manner as in Example 1, except that the copolymerization rate of polyethylene glycol having an average molecular weight of 1000 was changed.
比較例1は、平均分子量1000のポリエチレングリコ
ールの共重合率を4.5重量%とした場合(比較例1)
比較例2は、平均分子量1000のポリエチレングリ
コールの共重合率を1265重量%とした場合(比較例
2)であり、比較例3は、ポリエステルホモポリマーを
用いた場合(比較例3)である。Comparative Example 1 is a case where the copolymerization rate of polyethylene glycol having an average molecular weight of 1000 is 4.5% by weight (Comparative Example 1)
Comparative Example 2 is a case where the copolymerization rate of polyethylene glycol having an average molecular weight of 1000 is 1265% by weight (Comparative Example 2), and Comparative Example 3 is a case where a polyester homopolymer is used (Comparative Example 3).
延伸糸の単繊維強度は、順に、5.1g/d(比較例1
) 、2.8g/d (比較例2)、5.3g/d(比
較例3)であった。The single fiber strength of the drawn yarn was 5.1 g/d (Comparative Example 1).
), 2.8 g/d (Comparative Example 2), and 5.3 g/d (Comparative Example 3).
このようにして得られたポリエステル延伸糸を3本引揃
えて150Dにし、それぞれ24ゲージで靴下編地を編
成し、実施例1と同様の評価を行なった。また、複合繊
維糸を平織にし、染色仕上を行ない、実施例1と同様の
評価を行なった。なお、染色は比較例3のみ、キャリヤ
ーとしてテリールキャリャーV−10(明成化学■製)
を5%owf添加し、115℃、60分染色した。Three of the polyester drawn yarns thus obtained were aligned to have a diameter of 150D, each of which was knitted into a sock fabric with a 24 gauge, and evaluated in the same manner as in Example 1. In addition, the composite fiber yarn was made into a plain weave, dyed and finished, and evaluated in the same manner as in Example 1. In addition, only Comparative Example 3 was dyed, and the carrier was Teryl Carrier V-10 (manufactured by Meisei Kagaku ■).
5% owf was added and dyed at 115°C for 60 minutes.
実施例で得た試料(実施例1■、実施例1■、実施例1
■)は発色性、同色性にすぐれ、ソフトな風合で、強力
にも問題ない極めて良好な特性を示していた。Samples obtained in Examples (Example 1■, Example 1■, Example 1
Item (2) had excellent color development and color consistency, had a soft texture, and exhibited extremely good properties with no problem with strength.
一方、比較例で得た試料のうち、比較例1、比較例3は
常圧可染性を示さず、発色性が劣っていた。比較例2は
単繊維強度が低いという問題があった。On the other hand, among the samples obtained in Comparative Examples, Comparative Examples 1 and 3 did not exhibit normal pressure dyeability and had poor color development. Comparative Example 2 had a problem of low single fiber strength.
結果を表1に併せて示す。The results are also shown in Table 1.
(実施例2.比較例4)
平均分子量1000のポリエチレングリコールを8.0
重量%共重合した以外は実施例1と同様に重合、紡糸し
た。延伸は延伸時の熱板温度を120〜180℃に変更
しながら、延伸糸の沸収を6.7%(実施例2■)、9
.3%(実施例2■)、14.7%(実施例2■)に制
御し、製糸した。単繊維強度は順に5.0g/d、5.
0g/d、4.9g/dであり、収縮応力は0.70g
/d、0.69g/d、0゜62 g / dであった
。なお、延伸糸は75デニール、36フイラメントであ
り、常圧可染性を示していた。(Example 2. Comparative Example 4) Polyethylene glycol with an average molecular weight of 1000 was
Polymerization and spinning were carried out in the same manner as in Example 1, except that the weight percent copolymerization was carried out. Stretching was carried out by changing the hot plate temperature during stretching to 120 to 180°C and increasing the boiling yield of the drawn yarn to 6.7% (Example 2■), 9
.. It was controlled to 3% (Example 2■) and 14.7% (Example 2■), and yarn was produced. Single fiber strength is 5.0g/d, 5.
0g/d, 4.9g/d, and the shrinkage stress is 0.70g
/d, 0.69 g/d, and 0°62 g/d. The drawn yarn was 75 denier and had 36 filaments, and exhibited normal pressure dyeability.
次いで得られたポリエステル延伸糸をウール100%(
20OD相当)に精紡工程で第2図に示すようなサイロ
フィルタイブに複合繊維した。Next, the obtained polyester drawn yarn was made of 100% wool (
(equivalent to 20 OD) was made into a composite fiber in a spinning process into a silo filter tube as shown in Fig. 2.
得られた複合繊維糸は33番単糸、撚係数130、ポリ
エステル混率27重量%であった。The obtained composite fiber yarn was a No. 33 single yarn, a twist coefficient of 130, and a polyester blend ratio of 27% by weight.
次いで、該合撚糸を撚止めセットしたのち、タテおよび
ヨコ糸に用いてそれぞれ平織物に製織した。製織幅は1
70cm、タテ密度85本/吋、ヨコ密度72本/吋で
ある。Next, the combined twisted yarns were set to prevent twisting, and then used as warp and weft yarns to weave into plain weave fabrics. Weaving width is 1
70cm, vertical density 85 lines/inch, horizontal density 72 lines/inch.
次いで、染色条件以外は実施例1に従って、精練・熱処
理、洗絨、セット、染色し、仕上げ、評価した。Next, scouring/heat treatment, washing, setting, dyeing, finishing, and evaluation were performed according to Example 1 except for the dyeing conditions.
なお、染色は、分散染料Ka7alon Po1y B
lueFBL−E (日本化薬■)0.1%owf
、酸性染料KaYanol Milling Blue
BY (日本化薬■)0.1%owlを混合し、9
8℃、45分間、キャリヤーを用いることなく染色した
。結果を表2に示す。In addition, the dyeing is done using disperse dye Ka7alon Poly B.
lueFBL-E (Nippon Kayaku ■) 0.1%owf
, acid dye KaYanol Milling Blue
BY (Nippon Kayaku■) 0.1% owl was mixed, 9
Dyeing was carried out at 8° C. for 45 minutes without using a carrier. The results are shown in Table 2.
一方、比較磨きして、延伸時に熱板温度を高めて延伸糸
の沸収を2.8%に制御したもの(比較例4■)および
、熱板温度を低くして、沸収を25.1%にしたもの(
比較例4■)をそれぞれ実施例2に従って、同様に評価
した。結果を表2に示す。On the other hand, comparative polishing was performed in which the boiling yield of the drawn yarn was controlled to 2.8% by increasing the hot plate temperature during drawing (Comparative Example 4■), and the boiling yield was controlled to 25% by lowering the hot plate temperature. 1% (
Comparative Example 4■) was evaluated in the same manner as in Example 2. The results are shown in Table 2.
表2
実施例2で得た試料(実施例2■、実施例2■、実施例
2■)は、風合いにすぐれ、滑脱性にも問題ない極めて
良好な特性を示していた。Table 2 The samples obtained in Example 2 (Example 2 (2), Example 2 (2), and Example 2 (2)) had excellent texture and exhibited extremely good properties with no problems in slipping properties.
一方、比較例で得た試料のうち、比較例4■は滑脱性が
、比較例4■は風合がそれぞれ劣っていた。On the other hand, among the samples obtained in Comparative Examples, Comparative Example 4■ had poor sliding properties, and Comparative Example 4■ had poor texture.
(実施例3.比較例5)
平均分子量1000のポリエチレングリコールを7.5
重量%共重合した以外は実施例1と同様に重合、紡糸し
た。延伸は延伸時の熱板温度を120〜180℃に変更
し、更に、延伸糸を仮ヨリ加工機でスピンドルを用いず
連続走行させながら180〜2)0℃で熱処理を行ない
、4.0〜22.5%の範囲の沸収が異なる延伸糸を得
た。(Example 3. Comparative Example 5) Polyethylene glycol with an average molecular weight of 1000 was
Polymerization and spinning were carried out in the same manner as in Example 1, except that the weight percent copolymerization was carried out. For stretching, the hot plate temperature during stretching was changed to 120 to 180°C, and further heat treatment was performed at 180 to 2) 0°C while running the drawn yarn continuously in a temporary twisting machine without using a spindle. Drawn yarns with different boiling yields in the range of 22.5% were obtained.
延伸は非ケン縮の30デニール、12フイラメントであ
る。The drawing is 30 denier, 12 filaments without crimping.
次いで、沸収が異なる該延伸糸をエアーで交絡させて混
繊した。Next, the drawn yarns having different boiling yields were entangled with air to be mixed.
混繊糸は、沸収が6.2%の低収縮糸と15.9%の高
収縮糸の混繊糸(実施例3■)、沸収6.2%の低収縮
糸と沸収11,1%の高収縮糸の混繊糸(実施例3■)
、沸収4,0%の低収縮糸と沸収22.5%の混繊糸(
実施例3■)である。混繊糸の単繊維強度と収縮応力は
、それぞれ、5.2g/d、0.78g/d(実施例3
■)、5.1g/d、0.72g/d(実施例3■)
、4. 8 g/d、 0. 79 g/d (実施例
3■)であった。いずれも常圧可染性を示していた。The blended yarns include a blended yarn of a low shrinkage yarn with a boiling yield of 6.2% and a high shrinkage yarn of 15.9% (Example 3■), a blended yarn with a boiling yield of 6.2% low shrinkage yarn and a boiling yield 11 , 1% high shrinkage yarn mixed yarn (Example 3 ■)
, a low shrinkage yarn with a boiling point of 4.0% and a blended yarn with a boiling point of 22.5% (
Example 3). The single fiber strength and shrinkage stress of the mixed yarn were 5.2 g/d and 0.78 g/d, respectively (Example 3
■), 5.1g/d, 0.72g/d (Example 3■)
,4. 8 g/d, 0. 79 g/d (Example 3■). All exhibited dyeability under normal pressure.
次いで得られた混繊糸(60D、24フイラメント)に
ウール100%(113D相当)を精紡工程で図4に示
すようなシース・コアヤーンタイプに複合繊維した。得
られた合撚糸は52番単糸、ヨリ係数120、ポリエス
テルの混率34.7重量%である。Next, 100% wool (equivalent to 113D) was added to the obtained mixed fiber yarn (60D, 24 filaments) in a spinning process to form a composite fiber into a sheath/core yarn type as shown in FIG. 4. The obtained twisted yarn was a No. 52 single yarn, had a twist coefficient of 120, and had a polyester blend ratio of 34.7% by weight.
次いで、85℃、30分でヨリ止めセットしたのち、総
状で98℃、30分間スチーミング熱処理した。熱処理
は低張力で十分リラックスさせて行なった。Next, after being set at 85° C. for 30 minutes to prevent twisting, the entire structure was subjected to steam heat treatment at 98° C. for 30 minutes. The heat treatment was carried out under low tension and sufficiently relaxed.
次いで、パッケージ染色機でカセ染めを行ない、タテ、
ヨコに用いてそれぞれ平織物に製織し、精練、セットし
、仕上げた。なお、染色はブラウンの分散染料とブラウ
ンの酸性ミーリング染料を混合し、986C960分間
、キャリヤーを用いることなく行なった。Next, skein dyeing is performed using a package dyeing machine, and the vertical and
Each piece was woven horizontally into a plain weave, scoured, set, and finished. The dyeing was carried out using a mixture of brown disperse dye and brown acid milling dye for 986C960 minutes without using a carrier.
なお、仕上品の混繊糸のDFLは9.7%(実施例3■
)、4.9%(実施例3■)、18.5%(実施例3■
)であった。評価結果を表3に示す。The DFL of the finished mixed yarn is 9.7% (Example 3■
), 4.9% (Example 3■), 18.5% (Example 3■
)Met. The evaluation results are shown in Table 3.
一方、比較例として、DFLが0%のもの(比較例5■
)、2.2%のもの(比較例5■)を実施例と同様に評
価した。評価結果を表3に示す。On the other hand, as a comparative example, one with 0% DFL (Comparative Example 5)
), 2.2% (Comparative Example 5■) was evaluated in the same manner as in the Examples. The evaluation results are shown in Table 3.
表3
なタッチで、適度の張り、腰がある素晴しい風合であっ
た。Table 3 It had a nice touch, moderate tension, and a nice waist.
一方、比較例では、比較例5■は滑脱性が問題であった
。比較例5■は風合が粗硬で問題であった。On the other hand, in Comparative Example 5, slipping property was a problem. Comparative Example 5■ had a problem of rough and hard texture.
(実施例4.比較例6)
実施例1■で得た延伸糸を用い、複合繊維時の撚係数を
160(実施例4■)、110 (実施例4■)、20
0(実施例4■)の3条件に変えて、実施例1に従って
織物評価を行なった。なお、複合繊維での短繊維は、ウ
ールと5−ナトリウムスルホイソフタル酸を4.9モル
%共重合したポリエステル短繊維との混紡糸を用いた(
混紡率、ウール65重量%)。結果を表4に示す。(Example 4. Comparative Example 6) Using the drawn yarn obtained in Example 1■, the twist modulus of the composite fiber was 160 (Example 4■), 110 (Example 4■), and 20.
The fabric was evaluated according to Example 1 except for the three conditions of 0 (Example 4■). The short fibers used in the composite fibers were blended yarns of wool and polyester short fibers copolymerized with 4.9 mol% of 5-sodium sulfoisophthalic acid (
Blend rate, wool 65% by weight). The results are shown in Table 4.
実施例3で得た試料(実施例3■、実施例3■、実施例
3■)は、非常にふくらみ感のあるソフト表
一方、比較例として、撚係数80(比較例6■)および
250(比較例6■)をそれぞれ同様に評価し、結果を
表4に併せて示す。The samples obtained in Example 3 (Example 3■, Example 3■, Example 3■) had a soft surface with a very fluffy feeling, while the comparative examples had twist coefficients of 80 (Comparative Example 6■) and 250 (Comparative Example 6■) were evaluated in the same manner, and the results are also shown in Table 4.
実施例4で得られた試料(実施例4■、実施例4■、実
施例4■)は、風合にすぐれ、滑脱性にも問題がない、
極めてすぐれた特性を示していた。The samples obtained in Example 4 (Example 4■, Example 4■, Example 4■) had excellent texture and no problem with slipping properties.
It showed extremely excellent characteristics.
なお、ふくらみ感が大きい実施例4■は秋冬用途に、シ
ャリ味のある風合の実施例4■、実施例4■は春夏用途
に好適であった。Note that Example 4■, which had a large puffiness, was suitable for use in autumn and winter, and Examples 4■ and 4■, which had a crisp texture, were suitable for use in spring and summer.
一方、比較例では、比較例6■は滑脱性が、比較例6■
は硬い風合で、いずれも問題があった。On the other hand, in the comparative examples, Comparative Example 6■ has good sliding properties, while Comparative Example 6■
had a hard texture, and both had problems.
[発明の効果コ
本発明により、発色性、同色性にすぐれ、しかもすぐれ
た風合と物性を兼備えたポリエステルフィラメント糸と
ウールからなる複合繊維糸を提供することが可能となっ
た。[Effects of the Invention] According to the present invention, it has become possible to provide a composite fiber yarn made of polyester filament yarn and wool that has excellent color development and isochromaticity, as well as excellent texture and physical properties.
第1図〜第4図は、本発明のポリエステルフィラメント
糸とウールを主体とする短繊維の複合繊維糸の例を示す
。第1図はシース・コアヤーンタイプ、第2図はサイロ
フィルタイブ、第3図はカバーリングタイプ、第4図は
ポリエステル混繊糸のシース・コアヤーンタイプを示す
。なお、各図において(a)は側面図、(b)は断面図
を示す。
図中、
1:ポリエステルフィラメント
1′ ・混繊糸の低収縮糸
2:ウールを主体とする短繊維FIGS. 1 to 4 show examples of composite fiber yarns of the present invention made of short fibers mainly consisting of polyester filament yarns and wool. Fig. 1 shows a sheath/core yarn type, Fig. 2 shows a silo filter type, Fig. 3 shows a covering type, and Fig. 4 shows a sheath/core yarn type of polyester blend yarn. In each figure, (a) shows a side view, and (b) shows a cross-sectional view. In the figure, 1: Polyester filament 1' ・Low shrinkage yarn of mixed fiber yarn 2: Short fiber mainly made of wool
Claims (2)
合繊維糸であって、該ポリエステルが平均分子量500
〜4000のポリエチレングリコールを6.0〜10重
量%共重合した常圧可染性であり、単糸強度が3.0〜
6.0g/d、沸騰水収縮率が3〜23%、収縮応力が
0.3〜0.9g/dであり、ウールを主体とする短繊
維とヨリ係数100〜220の範囲で加熱されてなるこ
とを特徴とするポリエステルとウールの複合繊維糸。(1) Composite fiber yarn consisting of polyester filament yarn and wool, where the polyester has an average molecular weight of 500
~4000 polyethylene glycol is copolymerized with 6.0~10% by weight, dyeable under normal pressure, and has a single yarn strength of 3.0~
6.0 g/d, boiling water shrinkage rate of 3 to 23%, shrinkage stress of 0.3 to 0.9 g/d, and short fibers mainly made of wool with a twist coefficient of 100 to 220. A composite fiber yarn of polyester and wool that is characterized by the following properties:
合繊維糸であって、該ポリエステルが平均分子量500
〜4000のポリエチレングリコールを6.0〜10重
量%共重合した常圧可染性であり、且つ、該フィラメン
ト糸が低収縮糸と高収縮糸からなる混繊糸であり、ウー
ルを主体とする短繊維とヨリ係数100〜220の範囲
で加熱され、混繊糸の低収縮糸と高収縮糸の糸長差が3
〜20%であることを特徴とするポリエステルとウール
の複合繊維糸。(2) Composite fiber yarn consisting of polyester filament yarn and wool, the polyester having an average molecular weight of 500
~4000 copolymerized with 6.0~10% by weight of polyethylene glycol, dyeable under normal pressure, and the filament yarn is a mixed fiber yarn consisting of low shrinkage yarn and high shrinkage yarn, and is mainly made of wool. Short fibers are heated with a twist coefficient in the range of 100 to 220, and the yarn length difference between low shrinkage yarn and high shrinkage yarn of mixed fiber yarn is 3.
Composite fiber yarn of polyester and wool characterized by ~20%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2145077A JP2808829B2 (en) | 1990-05-31 | 1990-05-31 | Composite filament yarn of polyester filament yarn and wool |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2145077A JP2808829B2 (en) | 1990-05-31 | 1990-05-31 | Composite filament yarn of polyester filament yarn and wool |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0441732A true JPH0441732A (en) | 1992-02-12 |
JP2808829B2 JP2808829B2 (en) | 1998-10-08 |
Family
ID=15376854
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2145077A Expired - Fee Related JP2808829B2 (en) | 1990-05-31 | 1990-05-31 | Composite filament yarn of polyester filament yarn and wool |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2808829B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000012793A1 (en) * | 1998-08-28 | 2000-03-09 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
WO2001036722A1 (en) * | 1999-11-19 | 2001-05-25 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
WO2001036723A1 (en) * | 1999-11-19 | 2001-05-25 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US6509091B2 (en) | 1999-11-19 | 2003-01-21 | Wellman, Inc. | Polyethylene glycol modified polyester fibers |
US6582817B2 (en) | 1999-11-19 | 2003-06-24 | Wellman, Inc. | Nonwoven fabrics formed from polyethylene glycol modified polyester fibers and method for making the same |
US6623853B2 (en) | 1998-08-28 | 2003-09-23 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US8682230B2 (en) | 2010-09-03 | 2014-03-25 | Ricoh Company, Ltd. | Development device, process cartridge, and image forming apparatus including same having multiple recesses formed on a developer bearer |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101474691B1 (en) * | 2014-05-07 | 2014-12-31 | 성안합섬주식회사 | A Easy Dyable Polyester Yarn with Excellent Colorstrength and Method for Preparing the Same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5378384A (en) * | 1976-12-22 | 1978-07-11 | Hoechst Ag | Continuous dyeing of blended yarn fabric comprising modified polyester fiber and wool by monobath |
JPS58136821A (en) * | 1982-02-03 | 1983-08-15 | Asahi Chem Ind Co Ltd | Preparation of easily dyeable polyester fiber |
-
1990
- 1990-05-31 JP JP2145077A patent/JP2808829B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5378384A (en) * | 1976-12-22 | 1978-07-11 | Hoechst Ag | Continuous dyeing of blended yarn fabric comprising modified polyester fiber and wool by monobath |
JPS58136821A (en) * | 1982-02-03 | 1983-08-15 | Asahi Chem Ind Co Ltd | Preparation of easily dyeable polyester fiber |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000012793A1 (en) * | 1998-08-28 | 2000-03-09 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
US6623853B2 (en) | 1998-08-28 | 2003-09-23 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US6485829B2 (en) | 1998-08-28 | 2002-11-26 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
US6294254B1 (en) | 1998-08-28 | 2001-09-25 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
US6399705B2 (en) | 1999-11-19 | 2002-06-04 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
US6322886B2 (en) | 1999-11-19 | 2001-11-27 | Wellman, Inc. | Polyethylene glycol modified polyester fibers, yarns, and fabrics and method for making the same |
US6303739B2 (en) | 1999-11-19 | 2001-10-16 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
US6454982B1 (en) | 1999-11-19 | 2002-09-24 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
WO2001036723A1 (en) * | 1999-11-19 | 2001-05-25 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US6509091B2 (en) | 1999-11-19 | 2003-01-21 | Wellman, Inc. | Polyethylene glycol modified polyester fibers |
US6582817B2 (en) | 1999-11-19 | 2003-06-24 | Wellman, Inc. | Nonwoven fabrics formed from polyethylene glycol modified polyester fibers and method for making the same |
WO2001036722A1 (en) * | 1999-11-19 | 2001-05-25 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
US8682230B2 (en) | 2010-09-03 | 2014-03-25 | Ricoh Company, Ltd. | Development device, process cartridge, and image forming apparatus including same having multiple recesses formed on a developer bearer |
Also Published As
Publication number | Publication date |
---|---|
JP2808829B2 (en) | 1998-10-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2002086211A1 (en) | False twist yarn of polyester composite fiber and method for production thereof | |
EP0885988B1 (en) | Cloth having configurational stability and/or water resistance, and core/sheath type composite thread used therefor | |
JPH0441732A (en) | Composite fiber yarn of polyester fiber with wool | |
JPH03174076A (en) | Dyed textile made of blended polyester fiber and polyurethane fiber and production thereof | |
JP2932614B2 (en) | Polyester strong twist yarn | |
JPH0441738A (en) | Dyed fabric comprising polyester fiber and polyamide fiber cord and its preparation | |
JP2870769B2 (en) | Mixed fabric dyed product of polyester processed yarn and wool and method for producing the same | |
JP4252839B2 (en) | Acetate composite false twisted yarn and its twisted yarn and woven fabric using the same twisted yarn | |
JP3419578B2 (en) | Opaque fiber aggregate | |
JP3963356B2 (en) | Narrow fabric | |
JP3680723B2 (en) | Weaving fabric | |
JPH10251928A (en) | Composite spun yarn and cloth | |
JPH11315445A (en) | Woven and knitted fabric having excellent antistatic property, water absorption property, hygroscopic property and moisture releasing property | |
JP2926760B2 (en) | Polyester fiber mixed with vegetable fiber and dyed product of polyester fiber / plant fiber mixed fabric and method for producing the same | |
JPS61152849A (en) | Pile cloth for interior | |
JP3748462B2 (en) | Acetate hemp-tone composite false twisted yarn | |
JPH0219539A (en) | Combined polyester filament yarn fabric | |
JP2001164436A (en) | Polyester combined filament yarn and woven and knitted fabric using the same | |
JPH09157977A (en) | Composite yarn comprising polyester fiber and wool | |
JP4071533B2 (en) | Sewing products with a worn out appearance | |
JP2000256924A (en) | False twisted composite yarn | |
JP2022183505A (en) | Stretch woven fabric | |
JP4701478B2 (en) | Polychromatic composite processed yarn and method for producing the same | |
JP2013040422A (en) | False-twisted yarn and woven or knitted fabric including the same | |
JPH0369624A (en) | Polyester core and sheath conjugate false-twisted textured yarn |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |