JPH0284550A - Production of fibrillated knit or woven fabric - Google Patents
Production of fibrillated knit or woven fabricInfo
- Publication number
- JPH0284550A JPH0284550A JP20214588A JP20214588A JPH0284550A JP H0284550 A JPH0284550 A JP H0284550A JP 20214588 A JP20214588 A JP 20214588A JP 20214588 A JP20214588 A JP 20214588A JP H0284550 A JPH0284550 A JP H0284550A
- Authority
- JP
- Japan
- Prior art keywords
- component
- fibrillated
- polyamide
- fiber
- copolymerized
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 239000002759 woven fabric Substances 0.000 title abstract description 7
- 239000000835 fiber Substances 0.000 claims abstract description 36
- 239000004952 Polyamide Substances 0.000 claims abstract description 21
- 229920002647 polyamide Polymers 0.000 claims abstract description 21
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 239000002184 metal Substances 0.000 claims abstract description 7
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims abstract description 7
- 239000007864 aqueous solution Substances 0.000 claims abstract description 6
- 239000002131 composite material Substances 0.000 claims description 25
- 239000004744 fabric Substances 0.000 claims description 20
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 16
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 16
- -1 Polyethylene terephthalate Polymers 0.000 claims description 10
- 102000004169 proteins and genes Human genes 0.000 claims description 6
- 108090000623 proteins and genes Proteins 0.000 claims description 6
- 230000008961 swelling Effects 0.000 claims description 6
- 238000009941 weaving Methods 0.000 abstract description 6
- 210000002268 wool Anatomy 0.000 abstract description 6
- 230000002542 deteriorative effect Effects 0.000 abstract 1
- 208000016261 weight loss Diseases 0.000 abstract 1
- 239000013585 weight reducing agent Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 14
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- 206010061592 cardiac fibrillation Diseases 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 230000002600 fibrillogenic effect Effects 0.000 description 7
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 4
- 238000009940 knitting Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical class OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical compound O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 description 1
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920001410 Microfiber Polymers 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052976 metal sulfide Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000011824 nuclear material Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はフィブリル化法(分割法)を用いて細繊度糸か
らなる編織物を製造する方法に関し、更に詳しくは、ポ
リアミドと5染ポリエステルをフィブリル成分とする染
色性に優れたフィブリル化編織物の製造方法である。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a method for producing knitted fabrics made of fine yarns using a fibrillation method (splitting method), and more specifically, a method for producing knitted fabrics made of fine yarns using a fibrillation method (splitting method). This is a method for producing fibrillated knitted fabrics having excellent dyeability as fibril components.
(従来の技術)
従来、極めて細繊度の単糸(フィブリル)からなる編織
布や不織布によってスェード調の外観や柔軟な風合を有
する繊維構造物を特徴とする特許が数多く提案されてい
る。(Prior Art) Many patents have been proposed in the past that feature fiber structures that have a suede-like appearance and a soft texture made of knitted or nonwoven fabrics made of extremely fine single filaments (fibrils).
その1つに、フィブリル化型複合m維を用いて得た偏i
、l布や不織布に加熱処理や化学的処理を施して該複合
繊維を各成分に分割し、繊維構造物とする方法がある。One of them is the polarized i obtained using fibrillated composite m-fibers.
There is a method of subjecting a fabric or nonwoven fabric to heat treatment or chemical treatment to divide the composite fiber into each component to obtain a fibrous structure.
該フィブリル上型複合!a維としては、複数種の高分子
重合体が接合されたものを用いるが、一般にポリアミド
とポリエステルとが接合されたものを用いて、薬剤によ
りポリアミド膨潤収縮せしめてフィブリル化することが
行なわれている。(持分53−35633号公報)
しかし、通常のポリエステルは分散染料を用いて高温高
圧下で染色しなければならないため、ポリアミド成分を
汚染・劣化せしめることとなったり、他の繊維特に絹・
羊毛等の天然蛋白質繊維と混用することができなかった
りする欠点があった。The fibril supratype composite! A-fibers are made by bonding multiple types of high molecular weight polymers together, but generally polyamides and polyesters are bonded together and the polyamide is swollen and contracted with a chemical to form fibrils. There is. (Kibun No. 53-35633) However, since ordinary polyester must be dyed using disperse dyes under high temperature and high pressure, it may contaminate and deteriorate the polyamide component, and may cause damage to other fibers, especially silk, etc.
It has the disadvantage that it cannot be mixed with natural protein fibers such as wool.
このため、特開昭61−108786@公報には、イソ
フタル酸を共重合せしめ金属スルホネート基の濃度を1
.8〜4.0モルチとしたポリエステルを用いて、塩基
性染料で染色を行うと共に、スルボン基を導入したこと
によってポリアミドとの親和性が増大し、フィブリル化
し難くなる点を、イソフタル酸(金属スルホネート基)
a度を調整して解決することが開示されている。For this reason, Japanese Patent Application Laid-Open No. 108786/1986 discloses that isophthalic acid is copolymerized to reduce the concentration of metal sulfonate groups to 1.
.. Using polyester with a molarity of 8 to 4.0, it is dyed with a basic dye and isophthalic acid (metal sulfonate) is introduced, which increases its affinity with polyamide and makes it difficult to fibrillate. basis)
It is disclosed that the problem can be solved by adjusting the a degree.
(発明が解決しようとする課題)
しかしながら、前記従来技術に開示された方法では未だ
ポリアミドとの親和性が高いため、完全にフィブリル化
された編織物を得ることは難しい。(Problems to be Solved by the Invention) However, since the method disclosed in the prior art still has a high affinity with polyamide, it is difficult to obtain a completely fibrillated knitted fabric.
本発明はかかる欠点分解法するものであって、常温で充
分に染色され、しかも通常のフィブリル化処理によって
完全にフィブリル化でき、これらの工程でもamを劣化
させないため絹や羊毛等の天然蛋白質繊維とも混用可能
なフィブリル化m織物を提供することを目的とするもの
である。The present invention is a method for decomposing such defects, and is suitable for natural protein fibers such as silk and wool, which can be sufficiently dyed at room temperature, can be completely fibrillated by ordinary fibrillation treatment, and do not deteriorate AM even in these processes. The object of the present invention is to provide a fibrillated m-woven fabric that can be mixed with both.
(課題を解決するための手段)
本発明は、金属スルホネート基を有するイソフタル酸成
分を共重合したポリエチレンテレフタレートと、ポリア
ミドと単一フィラメントの横断面)こおいて一方の成分
が他方の成分を完全に包含しない形状で長手方向沿って
接合され、分割後の繊度が05デニール以下となるフィ
ブリル上型複合a維であ−って、しかもアルカリ水溶液
により共重合ポリエチレンテレフタレートの一部が減祉
された複合a維よりなる編織物とポリアミド膨潤剤によ
り処理し、該複合m紬のフィブリル化を行うことを特徴
とするもの又は、金属スルホネート基を有するイソフタ
ル酸成分を共重合したポリエチレンテレフタレートと、
ポリアミドとが単一フィラメントの横断面において一方
の成分が他方の成分全完全に包含しない形状で長手方向
沿って接合され、分割後の繊度が0.6デニール以下と
なるフィブリル上型複合a維にアルカリ水溶液を付与し
て共重合ポリエチレンテレフタレートの一部を減員した
後、天然蛋白質繊維と混用して編織を行い次いでm織物
をポリアミド膨潤剤により処理して、該複合*aのフィ
ブリル化を行うことを特徴とするものである。(Means for Solving the Problems) The present invention provides a cross section of polyethylene terephthalate copolymerized with an isophthalic acid component having a metal sulfonate group, a polyamide, and a single filament, in which one component completely covers the other component. Fibrillar type composite A fibers that are joined along the longitudinal direction in a shape that does not include the fibers and have a fineness of 0.5 denier or less after splitting, and in addition, a part of the copolymerized polyethylene terephthalate has been reduced by an aqueous alkaline solution. A knitted fabric made of composite A fibers is treated with a polyamide swelling agent to fibrillate the composite M pongee, or polyethylene terephthalate copolymerized with an isophthalic acid component having a metal sulfonate group;
The polyamide is joined along the longitudinal direction in a shape in which one component does not completely encompass the other component in the cross section of a single filament, and the fibril-type composite A fiber has a fineness of 0.6 denier or less after splitting. After reducing a part of the copolymerized polyethylene terephthalate by applying an alkaline aqueous solution, knitting and weaving it by mixing it with natural protein fiber, and then treating the m-woven fabric with a polyamide swelling agent to fibrillate the composite *a. It is characterized by:
本発明のフィブリル上型複合w4維は、ポリアミドとス
ルホネート基を有する塩基性染料可染型ポリエステル(
以下共重合PETと云う)とが接合されたものである。The superfibrillar composite W4 fiber of the present invention is made of polyamide and a basic dye-dyeable polyester having a sulfonate group (
(hereinafter referred to as copolymerized PET).
共重合PETは、共重合成分として、金属スルホード基
を有するイソフタル酸、A体的にはジメチルイソフタレ
ート、ビス−2−ヒドロキシエチルイソフタレート等の
スルホイソフタル酸を用い、これらを構成単位の80%
以上がエチレンテレフタレート或いはテトラメチレンテ
レフタレート等であるポリエステルに2〜5モル%程度
共重合せしめる。又、該共重合PETには、ポリアルキ
レングリコール等の第3成分を更に共重合せしめてもよ
く、例えば平均分子1500〜4000程度のポリエチ
レングリコールを5〜15Nji%程度共重合せしめれ
ば常温での染色が可能となる。Copolymerized PET uses isophthalic acid having a metal sulfide group as a copolymerization component, and sulfoisophthalic acids such as dimethyl isophthalate and bis-2-hydroxyethyl isophthalate are used as A-isomers, and these constitute 80% of the constituent units.
The above is copolymerized with a polyester such as ethylene terephthalate or tetramethylene terephthalate in an amount of about 2 to 5 mol %. Further, the copolymerized PET may be further copolymerized with a third component such as polyalkylene glycol. For example, if about 5 to 15 Nji% of polyethylene glycol with an average molecular weight of about 1500 to 4000 is copolymerized, Dyeing becomes possible.
ポリアミドとしては、例えば、ナイロン4、ナイロン8
、ナイロン7、ナイロン11、ナイロン12、ナイロン
68、ナイロン6−10、ポリメタキシレンアジパミド
、ポリパラキシリレンデカンアミド、ポリビスシクロへ
キシルメタンデカンアミド及びそれらを成分とするコポ
リアミドが挙げられるがナイロン6、ナイロン6Gが好
ましい。Examples of polyamides include nylon 4 and nylon 8.
, nylon 7, nylon 11, nylon 12, nylon 68, nylon 6-10, polymethaxylene adipamide, polyparaxylylene decanamide, polybiscyclohexylmethanedecanamide, and copolyamides containing these as components. Nylon 6 and nylon 6G are preferred.
複合繊維の形状としては、第1図(4)〜(ト)に示す
如く単一フィラメントの横断面において一方の成分が他
方の成分分完全に包含しない形状で長手方向に沿って接
合されたものであり、特に第1図(Q〜(ト)に示す如
く4〜8本の放射型形状のポリアミド成分と該放射状部
を補完する共重合PET成分とが接合されたものが好ま
しい。更に、両成分は以後に記載するフィブリル化処理
を行った後に、0.5デニール以下の細繊度とならなけ
れば本発明の目的とする柔軟な風合が得られない。The shape of the composite fiber is one in which one component does not completely encompass the other component in the cross section of a single filament, as shown in Figure 1 (4) to (g), and is joined along the longitudinal direction. In particular, as shown in FIG. Unless the components have a fineness of 0.5 denier or less after being subjected to the fibrillation treatment described below, the soft texture that is the object of the present invention cannot be obtained.
かかるフィブリル化型複合繊維は、共重合PET成分の
一部を溶解することにより減量する。溶解処理にはアル
カリ水溶液を用いるのが通常であり、苛性ソーダ、苛性
カリ、メタケイ酸ンーダ等が挙げられる。溶解処理は共
重合PET成分の全量に対して行ったり、ポリアミドと
の接着が剥れたりする程完全に行ってはならず、減量率
で4〜20重量%重量行程のが好ましい。又、アルカリ
溶解処理は繊維の状態で行なっても、編織後に行っても
よいが、アルカリによって溶解劣化する天然蛋白質繊維
と混用する場合は繊維の段階で事前に減量を行なう。Such fibrillated composite fibers are reduced in weight by dissolving a portion of the copolymerized PET component. In the dissolution treatment, an alkaline aqueous solution is usually used, and examples thereof include caustic soda, caustic potash, metasilicate powder, and the like. The dissolution treatment should not be carried out on the entire amount of the copolymerized PET component, nor should it be carried out so completely that the adhesive with the polyamide comes off, and it is preferable that the weight loss rate be 4 to 20% by weight. Further, the alkali dissolution treatment may be carried out in the fiber state or after knitting or weaving, but when used in combination with natural protein fibers which are degraded by dissolution by alkali, the weight should be reduced in advance at the fiber stage.
編織の際は、フィブリル化型複合副雑以ガにも他繊維を
用いてよいことは前記の如くであるが、特に天然繊維、
羊毛や絹等と混用すれば、フィブリル化して得られた極
細糸の柔軟な風合と天然l霜維の高級感ある風合の両方
が得られ好ましい。混用方法としては、交編織、混繊、
混紡、撚糸等如何なるものであってもよいが、交織の場
合経糸に天然aMIを、緯糸に複合tbt 16と用い
るとよい。As mentioned above, other fibers may be used for the fibrillated composite material during knitting, but natural fibers,
When mixed with wool, silk, etc., both the soft texture of fibrillated ultrafine fibers and the luxurious texture of natural frost fibers can be obtained, which is preferable. Mixing methods include interlacing, knitting and weaving, mixed fibers,
Any material such as blended yarn or twisted yarn may be used, but in the case of mixed weaving, it is preferable to use natural aMI for the warp and composite TBT 16 for the weft.
フィブリル化処理はポリアミド成分を膨潤収1宿せしめ
ることにより行う。ポリアミドの膨潤剤としてはベンジ
ルアルコール、β−フェニルエチルアルコール、フェノ
ール、m−クレゾール、am、酢酸等が挙げられ、水溶
液又は水性エマルジョンとして用いるのが適している。The fibrillation treatment is carried out by subjecting the polyamide component to a swelling capacity of 1. Swelling agents for polyamide include benzyl alcohol, β-phenylethyl alcohol, phenol, m-cresol, am, acetic acid, etc., and are suitable for use in the form of an aqueous solution or an aqueous emulsion.
特に以上の中でもベンジルアルコールの水性エマルジョ
ンと用いる方法が織物の収縮性やフィブリル化効果の点
で、また取扱いが比較釣合33な点で本発明方法には最
適である。Particularly, among the above methods, the method using an aqueous emulsion of benzyl alcohol is most suitable for the method of the present invention in terms of the shrinkability of the fabric and the fibrillation effect, and also because the handling is relatively balanced33.
上記フィブリル化剤の水性エマルジ冒ンを作るには、フ
ィブリル化剤に界面活性剤を添加して光透過率が50%
程度以下となるよう乳化分散させればよく、該界面活性
剤としては、ノニオン系活性剤、カチオン系活性剤、ア
ニオン系活性剤、両性活性剤、又はそれらの混合型等い
ずれでもよい。To make an aqueous emulsion of the above fibrillating agent, a surfactant is added to the fibrillating agent to achieve a light transmittance of 50%.
The surfactant may be a nonionic surfactant, a cationic surfactant, an anionic surfactant, an amphoteric surfactant, or a mixture thereof.
フィブリル化剤の濃度は、十分な収縮とフィブリル化効
果を得るためには1.6重量襲以上とする必要があり、
50重量%を超えると水性エマルジ璽ンの場合には不安
定となり、後のフィブリル化剤の除去が非常に困難とな
る。更に50iLtIbと超えるとポリアミド成分以外
の成分に悪影響を与える危険を生じる恐れがある。かか
る観点から該濃度は2.5〜20重量%であるのが好ま
しい。The concentration of the fibrillating agent needs to be at least 1.6% by weight in order to obtain sufficient shrinkage and fibrillating effects.
If it exceeds 50% by weight, the aqueous emulsion becomes unstable and subsequent removal of the fibrillating agent becomes extremely difficult. Furthermore, if it exceeds 50 iLtIb, there is a risk of adversely affecting components other than the polyamide component. From this point of view, the concentration is preferably 2.5 to 20% by weight.
本発明の方法では、上記のようなフィブリル化剤を含む
処理液中に被処理織物を浸漬放置するか、浸漬後マング
ル等により絞液するのが好適である。In the method of the present invention, it is preferable to leave the fabric to be treated immersed in a treatment liquid containing the fibrillating agent as described above, or to squeeze the fabric using a mangle or the like after dipping.
該処理液の温度は、6〜80°Cが望ましく、浸漬絞液
する場合、該布帛が保持するフィブリル化剤の量は、1
〜50重量%(対布帛Mm )が好ましい。一般にベン
ジルアルコール又はフェニルエチルアルコール分が低濃
度の場合(通常5%以下)は浸漬後加熱する方法が適し
ており(特に40゛C以下の温度の液に浸漬後10°C
以上に昇温する方法が有効である)。8%以上の場合は
パッディング法が適している。The temperature of the treatment liquid is preferably 6 to 80°C, and when the fabric is immersed and squeezed, the amount of fibrillating agent retained by the fabric is 1
~50% by weight (based on fabric Mm) is preferred. Generally, when the concentration of benzyl alcohol or phenylethyl alcohol is low (usually 5% or less), heating after immersion is suitable (especially at 10°C after immersing in a liquid with a temperature of 40°C or less).
(It is effective to raise the temperature above this level.) If it is 8% or more, the padding method is suitable.
(実施例)
実施例1
66ナイロンとポリエチレンテレフタレートにスルホイ
ソフタル酸を2,5モル襲、ポリエチレングリコール(
平均分子!1800)を71ffis共重合せしめた共
重合PETを1:3(容漬比)の割合で溶融接合紡糸し
たフィブリル化型複合フィラメント(第1図(E))を
チーズ巻きにして、2%苛性ソーダで80°Cで10分
間浸漬して放置することにより、共重合PET成分を1
6%減量させた。(Example) Example 1 Nylon 66 and polyethylene terephthalate were mixed with 2.5 moles of sulfoisophthalic acid, and polyethylene glycol (
Average molecule! A fibrillated composite filament (Fig. 1 (E)) prepared by melt spun spun copolymerized PET (1800) with 71 ffis at a ratio of 1:3 (soaking ratio) was wrapped in cheese, and was soaked in 2% caustic soda. By soaking and leaving at 80°C for 10 minutes, the copolymerized PET component
The weight was reduced by 6%.
その後、MMされたフィブリル型複合フィラメン)ヲf
fJJilこして、8%ペンジルアルコールエマルジ璽
ンに浸漬(30分で80゛Cまで昇温してそのまま20
分間浸漬して放置する方法でフィブリル化を行った。After that, the fibril-type composite filament (MM)
Strain it and soak it in 8% pendyl alcohol emulsion (heat up to 80°C in 30 minutes and leave it for 20 minutes).
Fibrillation was performed by dipping for a minute and leaving it for a while.
得られた編物は、非常に柔らかくふっくらとしており絹
様の風合会持つものであった。The obtained knitted fabric was extremely soft and fluffy, and had a silk-like texture.
実施例2
実施例1のフィブリル化型複合フィラメントを実施例1
と同ム)に減量させた後、経糸に48番手の羊毛を、緯
糸にフィブリル上型複合フィラメン1を用いて平織物を
製織した。Example 2 The fibrillated composite filament of Example 1 was
After reducing the weight to 100% by weight, a plain woven fabric was woven using No. 48 wool for the warp and fibril-type composite filament 1 for the weft.
該平織物をベンジルアルコール26袋、乳化剤25%の
エマルジョン液をこ浸漬し液保有率100襲となる様に
絞り取った後室温で2時間放置後水洗乾燥を行ない、得
られた織物を調べた所、非常に柔らかくふっくらとして
おり絹嫌の風合を持つものであった。The plain fabric was soaked in 26 bags of benzyl alcohol and an emulsion solution containing 25% emulsifier, squeezed out to a liquid retention rate of 100%, left at room temperature for 2 hours, washed with water and dried, and the resulting fabric was examined. However, it was extremely soft and fluffy, and had a texture similar to silk.
実施例3
実施例1のフィブリル化型複合フィラメントを実施例1
と同様に減量させた後、経糸に120番手の絹を、緯糸
にフィブリル化型複合フィラメントを用いて平織り企製
織した。Example 3 The fibrillated composite filament of Example 1 was
After reducing the weight in the same manner as above, plain weaving was carried out using 120 count silk for the warp and fibrillated composite filament for the weft.
核子ta 物にβ−フェニルエチルアルコール1%、乳
化剤2%のエマルジョン液に浸漬後30分で80°Cに
昇温しそのまま30分同処理した後、水洗乾燥して該織
物?調べた。After immersing the nuclear material in an emulsion solution containing 1% β-phenylethyl alcohol and 2% emulsifier, the temperature was raised to 80°C for 30 minutes, the same treatment was carried out for 30 minutes, and the fabric was then washed with water and dried. Examined.
得られた織物の風合は柔らかくふっくらとした風合であ
った
(発明の効果)
以上の如く、本発明に係るフィブリル化a維構造物は、
柔軟な風合と上品な光沢を有し、外衣用素材として極め
て有用なものであり、本発明はかかる素材を工業的に容
易に製造し得るものである。The texture of the obtained fabric was soft and fluffy (effect of the invention).As described above, the fibrillated a-fiber structure according to the present invention has the following properties:
It has a soft texture and an elegant luster, and is extremely useful as a material for outer clothing, and the present invention allows such a material to be easily produced industrially.
又、ポリエステル部分に常圧カチオン可染型の物を使用
しているため1ζ常圧で染色可能であり、羊毛及び絹等
の蛋白質yJ!imとの交織品が可能である。In addition, since the polyester part uses a material that can be dyed with normal pressure cations, it can be dyed with 1ζ normal pressure, and can be dyed with proteins such as wool and silk. Mixed woven products with im are possible.
第1図は本発明で用いるフィブリル化型複合繊維の横断
面を示す模式図である。
第 1
(A)
(B)
(C)
(D)
(E)
−33つFIG. 1 is a schematic diagram showing a cross section of a fibrillated composite fiber used in the present invention. 1st (A) (B) (C) (D) (E) -33
Claims (2)
共重合したポリエチレンテレフタレートと、ポリアミド
とが、単一フィラメントの横断面において一方の成分が
他方の成分を完全に包含しない形状で長手方向に沿って
接合され、分割後の繊度が0.5デニール以下となるフ
ィブリル化型複合繊維であって、しかもアルカリ水溶液
により共重合ポリエチレンテレフタレートの一部が減量
された複合繊維よりなる編織物をポリアミド膨潤剤によ
り処理し、該複合繊維のフィブリル化を行うことを特徴
とするフィブリル化編織物の製造方法。(1) Polyethylene terephthalate copolymerized with an isophthalic acid component having a metal sulfonate group and polyamide are bonded along the longitudinal direction in a shape in which one component does not completely encompass the other component in the cross section of a single filament. A knitted fabric made of a fibrillated composite fiber with a fineness of 0.5 denier or less after splitting, in which a part of the copolymerized polyethylene terephthalate has been reduced by an alkaline aqueous solution, is treated with a polyamide swelling agent. and fibrillating the composite fiber.
共重合したポリエチレンテレフタレートと、ポリアミド
とが単一フィラメントの横断面において一方の成分が他
方の成分を完全に包含しない形状で長手方向に沿って接
合され、分割後の繊度が0.5デニール以下となるフィ
ブリル化型複合繊維にアルカリ水溶液を付与して共重合
ポリエチレンテレフタレートの一部を減量した後、天然
蛋白質繊維と混用して編織を行い次いで編織物をポリア
ミド膨潤剤により処理して、該複合繊維のフィブリル化
を行うことを特徴とするフィブリル化編織物の製造方法
。(2) Polyethylene terephthalate copolymerized with an isophthalic acid component having a metal sulfonate group and polyamide are joined along the longitudinal direction in a shape in which one component does not completely encompass the other component in the cross section of a single filament. After applying an alkaline aqueous solution to fibrillated composite fibers with a fineness of 0.5 denier or less after splitting to reduce a portion of the copolymerized polyethylene terephthalate, the fibers are mixed with natural protein fibers and knitted, and then knitted fabrics are obtained. A method for producing a fibrillated knitted fabric, which comprises treating the composite fiber with a polyamide swelling agent to fibrillate the composite fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63202145A JPH0653993B2 (en) | 1988-08-12 | 1988-08-12 | Method for producing fibrillated knitted fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63202145A JPH0653993B2 (en) | 1988-08-12 | 1988-08-12 | Method for producing fibrillated knitted fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0284550A true JPH0284550A (en) | 1990-03-26 |
JPH0653993B2 JPH0653993B2 (en) | 1994-07-20 |
Family
ID=16452707
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63202145A Expired - Lifetime JPH0653993B2 (en) | 1988-08-12 | 1988-08-12 | Method for producing fibrillated knitted fabric |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0653993B2 (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6385166A (en) * | 1986-09-22 | 1988-04-15 | 帝人株式会社 | Production of ultrafine fiber knitted fabric |
-
1988
- 1988-08-12 JP JP63202145A patent/JPH0653993B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6385166A (en) * | 1986-09-22 | 1988-04-15 | 帝人株式会社 | Production of ultrafine fiber knitted fabric |
Also Published As
Publication number | Publication date |
---|---|
JPH0653993B2 (en) | 1994-07-20 |
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