JPH04263679A - Production of opal finishing cloth - Google Patents
Production of opal finishing clothInfo
- Publication number
- JPH04263679A JPH04263679A JP4247891A JP4247891A JPH04263679A JP H04263679 A JPH04263679 A JP H04263679A JP 4247891 A JP4247891 A JP 4247891A JP 4247891 A JP4247891 A JP 4247891A JP H04263679 A JPH04263679 A JP H04263679A
- Authority
- JP
- Japan
- Prior art keywords
- printing
- polyester
- woven
- fabric
- nylon
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 39
- 239000011022 opal Substances 0.000 title claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 229920000728 polyester Polymers 0.000 claims abstract description 26
- 239000000835 fiber Substances 0.000 claims abstract description 21
- 239000002904 solvent Substances 0.000 claims abstract description 14
- 239000004952 Polyamide Substances 0.000 claims abstract description 11
- 229920002647 polyamide Polymers 0.000 claims abstract description 11
- 239000002131 composite material Substances 0.000 claims description 11
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims description 4
- 238000007639 printing Methods 0.000 abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 12
- 238000010025 steaming Methods 0.000 abstract description 5
- 239000003513 alkali Substances 0.000 abstract description 4
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000661 sodium alginate Substances 0.000 abstract description 3
- 235000010413 sodium alginate Nutrition 0.000 abstract description 3
- 229940005550 sodium alginate Drugs 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 229920001778 nylon Polymers 0.000 description 16
- 239000004677 Nylon Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 12
- 238000005406 washing Methods 0.000 description 9
- 238000001035 drying Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- 239000012209 synthetic fiber Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000010017 direct printing Methods 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000009940 knitting Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000009991 scouring Methods 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229920001410 Microfiber Polymers 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- -1 diol compound Chemical class 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000010022 rotary screen printing Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 101100446303 Caenorhabditis elegans fbl-1 gene Proteins 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 101150037491 SOL1 gene Proteins 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000010018 discharge printing Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000009981 jet dyeing Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 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
- MTZWHHIREPJPTG-UHFFFAOYSA-N phorone Chemical compound CC(C)=CC(=O)C=C(C)C MTZWHHIREPJPTG-UHFFFAOYSA-N 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010019 resist printing Methods 0.000 description 1
- 238000010020 roller printing Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Landscapes
- Decoration Of Textiles (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は新規な織編物及びその製
造方法に関する。詳しくはポリエステルとポリアミドか
ら成る分割型複合糸を用いた織編物に一成分を溶解させ
る溶剤をプリントすることにより一成分を溶解し、他成
分だけを残す新規な風合と光透過性のある織編物の製造
方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel woven or knitted fabric and a method for producing the same. In detail, by printing a solvent that dissolves one component on a woven or knitted fabric using splittable composite yarns made of polyester and polyamide, we have created a new texture and light-transmitting fabric that dissolves one component and leaves only the other component. This invention relates to a method for producing knitted fabrics.
【0002】0002
【従来の技術】従来オパール加工は合成繊維(ポリエス
テル、ナイロン)とセルロース系繊維の混紡、交織編布
を強酸によってセルロース系繊維にダメージを与え、合
成繊維だけを残す方法やポリエステルとナイロンの交織
布を強アルカリでポリエステルを溶解し、ナイロンだけ
を残す方法やポリエステル成分の違いによりアルカリの
溶解速度差を利用してオパール布を得る方法である。し
かしこれらの方法では交織、交編の場合系が太くなり厚
地織物に限定されたり、ポリエステルの溶解速度を利用
する場合は強力に問題があったり、経糸、緯糸の一部を
溶解するには交撚や混紡する必要があったりし、風合、
生地の厚味、コスト的に問題があった。また近年合成繊
維の極細化技術が大巾に進歩しドレープ性にすぐれた織
編物が得られるようになった。極細繊維が一般に普及す
るようになると差別化が要求され、織編物の表面変化が
必要になっている。[Prior art] Conventional opal processing involves methods such as blending synthetic fibers (polyester, nylon) and cellulose fibers, or using strong acid to damage the cellulose fibers, leaving only the synthetic fibers, or blending or knitting fabrics of synthetic fibers (polyester, nylon) and cellulose fibers. Opal cloth can be obtained by dissolving polyester with strong alkali and leaving only nylon, or by utilizing the difference in dissolution rate of alkali depending on the polyester component. However, with these methods, the system becomes thicker in the case of mixed weaving and mixed knitting, and is limited to thick fabrics, and there are strong problems when using the dissolution rate of polyester, and mixing is required to dissolve part of the warp and weft. It may be necessary to twist or blend, and the texture,
There were problems with the thickness of the dough and the cost. Furthermore, in recent years, advances in ultrafine synthetic fiber technology have made it possible to obtain woven and knitted fabrics with excellent drape properties. As ultrafine fibers become popular, differentiation is required, and surface changes in woven and knitted fabrics are required.
【0003】0003
【発明が解決しようとする課題】本発明はかかる従来の
方法とは異なり、薄地織編物でもソフトな風合で安価に
でき、しかも極細繊維に表面変化をもたせた織編物を提
供するものである。[Problems to be Solved by the Invention] Unlike such conventional methods, the present invention provides a woven or knitted fabric that can be produced at low cost with a soft texture even if it is a thin woven or knitted fabric, and in which the ultrafine fibers have a surface change. .
【0004】0004
【課題を解決するための手段】本発明は上記問題点を解
決するために次のような構成を有する。[Means for Solving the Problems] In order to solve the above problems, the present invention has the following configuration.
【0005】即ち、ポリアミドとポリエステルからなる
分割型複合繊維を用いた織編物に、一成分を溶解させる
溶剤を用いてプリントすることにより部分的にポリエス
テル又はナイロンを溶解し、その後割繊加工することを
特徴とするオパール加工布の製造法である。That is, a woven or knitted fabric using a splittable composite fiber made of polyamide and polyester is printed using a solvent that dissolves one component, thereby partially dissolving the polyester or nylon, and then splitting the fabric. This is a method for producing opal-treated cloth characterized by:
【0006】本発明における分割型複合繊維とは、隣接
型複合繊維や放射状型複合繊維およびそれらの異形断面
繊維や中空繊維等が挙げられる。これら複合繊維の分割
成分と被分割成分の組合せについては特に限定されるも
のではないが、相互親和性に乏しいポリマーの組合せで
あることが好ましい。ポリアミドとポリエステルの組合
せが好適に用いられる。好適に用いられるポリアミドと
しては、例えば、ナイロン6、ナイロン10、ナイロン
11、ナイロン12、ナイロン66、ナイロン610お
よびこれらを主成分とする共重合ポリアミドなどが挙げ
られるが中でもナイロン6やナイロン66が好ましく用
いられる。また好適に用いられるポリエステルとしては
、例えば、テレフタル酸、イソフタル酸、ナフタリン−
2,6−ジカルボン酸などの芳香族ジカルボン酸、もし
くはアジピン酸、セバシン酸などの脂肪族ジカルボン酸
とエチレングリコールなどのジオール、ネオペンチルグ
リコールなどのジオール化合物とから合成されるポリエ
ステルが好ましく用いられる。The splittable conjugate fibers in the present invention include adjacent conjugate fibers, radial conjugate fibers, irregular cross-section fibers, hollow fibers, and the like. Although the combination of the splitting component and the splitting component of these composite fibers is not particularly limited, it is preferably a combination of polymers that have poor mutual affinity. A combination of polyamide and polyester is preferably used. Suitable polyamides include, for example, nylon 6, nylon 10, nylon 11, nylon 12, nylon 66, nylon 610, and copolyamides containing these as main components, with nylon 6 and nylon 66 being preferred. used. Examples of polyesters that can be suitably used include terephthalic acid, isophthalic acid, and naphthalic acid.
A polyester synthesized from an aromatic dicarboxylic acid such as 2,6-dicarboxylic acid or an aliphatic dicarboxylic acid such as adipic acid or sebacic acid and a diol such as ethylene glycol or a diol compound such as neopentyl glycol is preferably used.
【0007】上述のような複合繊維を用いて作られる織
編物の組織としては特に限定されるものではないが、平
織、綾織、マットあるいはトリコット、スムースなどの
組織が挙げられる。[0007] The texture of the woven or knitted fabric made using the above-mentioned composite fibers is not particularly limited, but includes plain weave, twill weave, matte, tricot, and smooth textures.
【0008】本発明における一成分を溶解させる溶剤と
はアルカリ剤ではポリエステルの溶剤となる、水酸化ナ
トリウム、炭酸ナトリウム、ケイ酸ナトリウム等が含ま
れるが、これに限定されるものではなく、また、酸では
ナイロンの溶剤である蟻酸、酢酸等が含まれる。[0008] In the present invention, the solvent for dissolving one component includes, but is not limited to, sodium hydroxide, sodium carbonate, sodium silicate, etc., which are solvents for polyester in the case of alkaline agents. Acids include formic acid, acetic acid, etc., which are solvents for nylon.
【0009】本発明でいうプリントとは溶剤を含んだ糊
剤を生地に直接捺染することをいう。捺染後乾燥しスチ
ーミング工程を通過させることにより、部分的にポリエ
ステル又はナイロンが溶解する。直接捺染はハンドプリ
ント、ローラープリント、スクリーンプリント、ロータ
リースクリーンプリント等が含まれる。プリントに用い
る糊剤はポリエステル、ナイロンの溶剤によりゲル化や
粘度低下のないものが好ましい。例えばアルギン酸ソー
ダ、CMC、ローガストビーンガム、グアガム、澱粉等
がある。この糊剤の中にポリエステル、ナイロンの溶剤
を入れて直接捺染するが、糊剤の中にポリエステル又は
ナイロンを染色するための染料や染料溶解剤、染着増進
剤(キャリヤー)溶解促進剤を含ませることも可能であ
る。Printing in the present invention refers to directly printing a paste containing a solvent onto a fabric. After printing, the polyester or nylon is partially dissolved by drying and passing through a steaming process. Direct printing includes hand printing, roller printing, screen printing, rotary screen printing, etc. The adhesive used for printing is preferably one that does not gel or reduce viscosity due to polyester or nylon solvents. Examples include sodium alginate, CMC, raw bean gum, guar gum, and starch. A solvent for polyester or nylon is added to this paste for direct printing, but the paste also contains dyes, dye dissolvers, dye accelerators (carriers), and dissolution promoters for dyeing polyester or nylon. It is also possible to
【0010】分割型複合繊維から成る織編物をポリエス
テルやナイロンの溶剤を用いずに精練し、生地の形態を
安定させた後に必要によりポリエステル又はナイロンの
一方又は両者を染める。その後、前述の方法でプリント
する。プリントは直接捺染(オーバープリント)が好ま
しいが、防染、抜染法の併用も可能である。プリント後
乾燥するが、この場合、乾燥工程でポリエステル又はナ
イロンのプリント部分の一部がすでに溶解するので過激
な条件は好ましくない。シリンダー乾燥、ホットフルー
乾燥機、テンションレス熱風乾燥機等で行なうが乾燥温
度は80〜160℃、さらに好ましくは100〜140
℃である。その後スチーミング処理により、ナイロン、
ポリエステルを溶解させ、必要により染着も行なう。ス
チーミングは飽和蒸気、過飽和蒸気のどちらでもよい、
飽和蒸気ならば100〜135℃、過飽和蒸気ならば1
30℃〜200℃が好ましい。スチーミング処理後、湯
洗、水洗により、溶解したポリエステル、ナイロンを生
地より脱落させるため、超音波や生地のビーティングを
用いることが容易に速く処理する方法である。その後、
割繊加工するが、プリント前に割繊加工するとプリント
工程により、ふくらみや生地の携帯安定性がそこなわれ
るため、プリント後に割繊加工することは本発明の重要
なポイントである。またプリント時に発生する割繊糸の
損障(スレ、当り等)を防止することができる。割繊処
理方法は、ポリエステルとポリアミドからなる分割型複
合繊維をベンジルアルコールなどの乳化分散液で処理す
る方法やポリエステルとポリアミドから成る分割型複合
繊維のポリエステル側を膨潤し分割した後、熱処理で収
縮させる方法や相互に親和性の乏しい複合種のポリマー
からなる分割型複合繊維を用いた織編物を圧縮処理し、
ついでポリマーの一成分を膨潤させる薬剤を含む液流中
で揉み処理する方法等が例示される。この他にアルカリ
でポリエステルを一部溶解し分割させることもできる。
本発明でいうオパール加工とは複数成分から成る素材の
一部を一成分の溶剤を用いて溶解させることにより、加
工部分の表面変化が得られ、加工をしていない部分と加
工した部分では光透過性が異なり、風合もソフトになる
。[0010] A woven or knitted fabric made of splittable composite fibers is refined without using a polyester or nylon solvent, and after the form of the fabric is stabilized, one or both of the polyester and nylon is dyed, if necessary. Then print using the method described above. Direct printing (overprinting) is preferred for printing, but resist printing and discharge printing methods can also be used in combination. After printing, it is dried, but in this case, extreme conditions are not preferred since some of the polyester or nylon printed parts are already dissolved during the drying process. The drying is carried out using a cylinder dryer, a hot flue dryer, a tensionless hot air dryer, etc., and the drying temperature is 80 to 160°C, more preferably 100 to 140°C.
It is ℃. After that, nylon,
The polyester is dissolved and dyed if necessary. Steaming can be done with either saturated steam or supersaturated steam.
100-135℃ for saturated steam, 1 for supersaturated steam
30°C to 200°C is preferred. After the steaming process, the dissolved polyester and nylon are removed from the fabric by washing with hot water or water, so using ultrasonic waves or beating the fabric is an easy and fast processing method. after that,
However, splitting the fibers before printing will damage the bulge and carrying stability of the fabric during the printing process, so splitting the fabric after printing is an important point of the present invention. Furthermore, it is possible to prevent damage to the split yarn (scratching, hitting, etc.) that occurs during printing. Splitting treatment methods include treating splittable conjugate fibers made of polyester and polyamide with an emulsified dispersion such as benzyl alcohol, or swelling and splitting the polyester side of splittable conjugate fibers made of polyester and polyamide, and then shrinking by heat treatment. Compression treatment of woven and knitted fabrics using splittable composite fibers made of composite types of polymers with poor mutual affinity,
Examples include a method in which one component of the polymer is then rubbed in a liquid stream containing a drug that swells it. Alternatively, polyester can be partially dissolved and divided with an alkali. Opal processing as referred to in the present invention is a process in which a part of a material consisting of multiple components is dissolved using a single-component solvent to obtain a surface change in the processed part, and the unprocessed part and the processed part are exposed to light. The transparency is different and the texture is softer.
【0011】[0011]
【実施例】以下、実施例により本発明を詳細に説明する
。
実施例
分割成分化ポリアミド70%、被分割成分がポリエステ
ル30%で分割後の単糸繊度がそれぞれ0.6デニール
と0.4デニールとなるように8分割の分割型複合繊維
75dを経緯糸に用いて綾組織の織物を得た。次に得ら
れた織物をオープンソーパーを用いて下記の条件で精練
を行った。
(精練条件)
非イオン界面活性剤 1g/l トリポリリン酸
ソーダ 1g/l
95℃×20sec
その後同じオープンソーパーで8秒間の水洗を行った。
次いでショートループを用いて130℃×90sec
の乾燥を行った。オートスクリーン捺染機で下記の条件
でプリントを小柄な花模様で行った。
プリント部分の糊付着景を160g/m2になるよ
うにスケージの形や印捺圧の調整を行った。印捺後すぐ
にホットフルー乾燥を行い、その後高圧スチーマで13
0℃×20分スチーミング処理をした。その後連続ウィ
ンス機を使って水洗を行った。この時水洗効果をよくす
るため超音波洗浄を2、3槽目に設定した。この時の生
地の状態はプリント部分はナイロンが残り、光透過性が
よくなっている。非プリント部分は割繊されていないの
で平べったい硬い織物である。割繊処理は下記の条件で
液流染色機を用いて行った。
(割繊条件)
NaOH(38Be′) 10% sol1
20℃×30分 浴比1:10その
後、中和処理、水洗、乾燥を通常の方法で行った。
プリントを行った花柄の部分が他に比べシースルー状に
なりオパール加工特有の表面効果となった。オーパール
加工していない部分はスレ当りのない美しい表面である
。比較例として同条件で織物→割繊加工→オーパール加
工したものはスレ、当りが著しく発生し、商品価値の少
ないものである。又風合も本発明品に比べ薄い感じのす
るボリューム感のないものである。
オハ゜ール加工表面 ス
レ当り 風合 織物→オハ゜ール加工→割繊加工(
実施例1) ○ ○
○織物→割繊加工→オハ゜ール加工(比較例1
) ○ ×
×[Examples] The present invention will be explained in detail below with reference to Examples. Example: 70% split polyamide component, 30% polyester component to be split, 8 split split composite fibers 75d were made into warp and warp so that the single fiber fineness after splitting was 0.6 denier and 0.4 denier, respectively. A woven fabric with a twill structure was obtained using the method. Next, the obtained fabric was scoured using an open soaper under the following conditions. (Scouring conditions) Nonionic surfactant 1 g/l Sodium tripolyphosphate 1 g/l 95° C. x 20 sec Thereafter, water washing was performed for 8 seconds using the same open soaper. Then, using a short loop at 130°C x 90 seconds
was dried. A small flower pattern was printed using an auto screen printing machine under the following conditions. The shape of the scale and the printing pressure were adjusted so that the adhesive adhesion of the printed part was 160 g/m2. Immediately after printing, hot-fluid drying is performed, followed by high-pressure steamer drying for 13 minutes.
Steaming treatment was performed at 0°C for 20 minutes. After that, water washing was performed using a continuous wince machine. At this time, ultrasonic cleaning was set in the second and third baths to improve the water washing effect. The condition of the fabric at this time is that the nylon remains in the printed area and has good light transparency. The non-printed part is not split, so it is a flat, stiff fabric. The splitting process was performed using a jet dyeing machine under the following conditions. (Splitting conditions) NaOH (38Be') 10% sol1
20° C. x 30 minutes at a bath ratio of 1:10. Thereafter, neutralization treatment, washing with water, and drying were performed in the usual manner. The printed floral pattern is more see-through than the other parts, creating a surface effect unique to opal processing. The part that is not opalized has a beautiful surface with no scratches. As a comparative example, a fabric that was processed under the same conditions by woven fabric, splitting processing, and opal processing had significant scratches and scratches, and had little commercial value. Also, the texture is thinner and less voluminous than the product of the present invention.
Ohaal processing surface per thread Texture Fabric → Ohaal processing → Splitting processing (
Example 1) ○ ○
○Woven fabric → Split processing → Ohal processing (Comparative example 1)
) ○ ×
×
【0012】実施例
実施例1と同じ糸を用いて28ゲージスムースを編んだ
。得られたニットをウィンスを用いて精練を行った。
精練条件
非イオン界面活性剤 1g/l
95℃×15分 浴
比1:30その後同じウィンスを用いて40℃×10分
2回水洗を行った。次いでショートループドライヤ
ーで120℃×2分の乾燥をした。ロータリースクリー
ン捺染機を用いて直径2cm程度の水玉状のプリントを
行った。プリント条件は下記の通りである。
SUMINOL MILL RED RS(
住友化学製) 3部 NaOH(38
Be′)
10部 アルギ
ン酸ソーダ(12%)
60部 水
27部
合 計
100部プリント部分の糊
付着量を150g/m2になるようにプリント条件を調
整した。印捺後120℃×90秒で熱風乾燥を行った。
その後精練の時に行ったウィンスで湯洗水洗を行った。
湯洗条件は非イオン界面活性剤1g/l Na2 CO
3 0.5g/l 浴比1:35 60℃×15分
である。その後常温の水で5分×2回水洗した。
割繊条件はベンジルアルコール 20サンモール
BK(日華化学製) 2で水中に乳化分散させた浴で
ウィンスを用いて浴比に30 95℃×30分の条件
で行った。その後CH3 COOHで中和処理を行った
後、染色をした。
Foron Blue FBL 1%o
wf分散剤
0.5%owfCH3 COOH
0.3%owf
浴比1:15 130℃×20分染色は液洗染色
機を使用した。その後、水洗、乾燥は通常の方法で行っ
た。比較例2として編物→割繊→染色→オパール加工を
同条件で行った。
オパール加
工表面 スレ、当り 風合 実
施例2 ○
○ ○ 比較
例2 ○
× ×Example 28 gauge smooth was knitted using the same yarn as in Example 1. The obtained knit was refined using a wince. Scouring conditions Nonionic surfactant 1g/l
95°C x 15 minutes, bath ratio 1:30, and then water washing was performed twice at 40°C x 10 minutes using the same wince. Next, it was dried at 120° C. for 2 minutes using a short loop dryer. A polka dot shape with a diameter of about 2 cm was printed using a rotary screen printing machine. The printing conditions are as follows. SUMINOL MILL RED RS (
(manufactured by Sumitomo Chemical) 3 parts NaOH (38
Be')
10 parts Sodium alginate (12%)
60 parts water
27 parts
total
Printing conditions were adjusted so that the amount of glue adhered to the 100-copy portion was 150 g/m2. After printing, hot air drying was performed at 120° C. for 90 seconds. After that, I washed it with hot water and cold water using the Wins that I had used during scouring. Hot water washing conditions: nonionic surfactant 1g/l Na2 CO
3 0.5 g/l Bath ratio 1:35 60°C x 15 minutes. Thereafter, it was washed twice with water at room temperature for 5 minutes. The fiber splitting was performed using a bath in which benzyl alcohol 20 Sunmol BK (manufactured by NICCA Chemical Co., Ltd.) was emulsified and dispersed in water at a bath ratio of 30 to 95° C. for 30 minutes using a wince. After that, it was neutralized with CH3 COOH and then stained. Foron Blue FBL 1%o
wf dispersant
0.5%owfCH3 COOH
0.3%owf
A liquid washing dyeing machine was used for dyeing at 130° C. for 20 minutes at a bath ratio of 1:15. Thereafter, water washing and drying were performed in the usual manner. As Comparative Example 2, knitting → splitting → dyeing → opal processing was performed under the same conditions. Opalized surface Scratches, hits Texture Example 2 ○
○ ○ Comparative example 2 ○
× ×
【0013】[0013]
【発明の効果】ポリアミドとポリエステルから成る分割
型複合繊維を一成分を溶解させる溶剤でプリントするこ
とにより、一成分を溶解させ、他成分を残し、その後、
分割型複合繊維を分割させるための割繊加工を行うこと
により、品質の安定した表面変化のあるソフトな織編物
を得ることができる。[Effect of the invention] By printing splittable composite fibers made of polyamide and polyester with a solvent that dissolves one component, one component is dissolved and the other component is left behind, and then,
By splitting the splittable composite fibers, a soft woven or knitted fabric with stable quality and surface changes can be obtained.
Claims (1)
割型複合繊維を用いた織編物に、一成分を溶解させる溶
剤を用いてプリントすることにより、部分的にポリエス
テル又はポリアミドを溶解し、その後割繊加工をするこ
とを特徴とするオパール加工布の製造方法。Claim 1: A woven or knitted fabric using a splittable composite fiber made of polyamide and polyester is printed using a solvent that dissolves one component, thereby partially dissolving the polyester or polyamide, and then splitting the fabric. A method for producing an opal-treated cloth characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4247891A JPH04263679A (en) | 1991-02-13 | 1991-02-13 | Production of opal finishing cloth |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4247891A JPH04263679A (en) | 1991-02-13 | 1991-02-13 | Production of opal finishing cloth |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04263679A true JPH04263679A (en) | 1992-09-18 |
Family
ID=12637175
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4247891A Pending JPH04263679A (en) | 1991-02-13 | 1991-02-13 | Production of opal finishing cloth |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04263679A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007049710A1 (en) * | 2005-10-27 | 2007-05-03 | Seiren Co., Ltd. | Opal-finished fabric |
| WO2012008548A1 (en) * | 2010-07-14 | 2012-01-19 | Kbセーレン株式会社 | Core-sheath type composite fiber |
-
1991
- 1991-02-13 JP JP4247891A patent/JPH04263679A/en active Pending
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007049710A1 (en) * | 2005-10-27 | 2007-05-03 | Seiren Co., Ltd. | Opal-finished fabric |
| US8076253B2 (en) | 2005-10-27 | 2011-12-13 | Seiren Co., Ltd. | Opal-finished fabric |
| JP5006792B2 (en) * | 2005-10-27 | 2012-08-22 | セーレン株式会社 | Opal processed fabric |
| WO2012008548A1 (en) * | 2010-07-14 | 2012-01-19 | Kbセーレン株式会社 | Core-sheath type composite fiber |
| WO2012008617A1 (en) * | 2010-07-14 | 2012-01-19 | セーレン株式会社 | Fibrous fabric and manufacturing method for same |
| JPWO2012008548A1 (en) * | 2010-07-14 | 2013-09-09 | Kbセーレン株式会社 | Core-sheath type composite fiber |
| JPWO2012008617A1 (en) * | 2010-07-14 | 2013-09-09 | セーレン株式会社 | Fiber fabric and method for producing fiber fabric |
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