JPH04281051A - Knitted fabric excellent in dimensional stability - Google Patents
Knitted fabric excellent in dimensional stabilityInfo
- Publication number
- JPH04281051A JPH04281051A JP7254491A JP7254491A JPH04281051A JP H04281051 A JPH04281051 A JP H04281051A JP 7254491 A JP7254491 A JP 7254491A JP 7254491 A JP7254491 A JP 7254491A JP H04281051 A JPH04281051 A JP H04281051A
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- solvent
- knitted fabric
- yarn
- acrylic
- 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 28
- 229920002972 Acrylic fiber Polymers 0.000 claims abstract description 34
- 239000000835 fiber Substances 0.000 claims abstract description 30
- 239000002904 solvent Substances 0.000 claims abstract description 22
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 27
- 238000002156 mixing Methods 0.000 abstract description 9
- 238000001035 drying Methods 0.000 abstract description 7
- 239000000981 basic dye Substances 0.000 abstract description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 2
- 229920002821 Modacrylic Polymers 0.000 abstract 3
- 238000009987 spinning Methods 0.000 description 13
- 238000009940 knitting Methods 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 6
- 238000005259 measurement Methods 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- -1 polypropylene Polymers 0.000 description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- VRAHSRHQTRYBJV-UHFFFAOYSA-M sodium;2-methyl-1-oxoprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)C(=O)S([O-])(=O)=O VRAHSRHQTRYBJV-UHFFFAOYSA-M 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- FKOZPUORKCHONH-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid Chemical compound CC(C)CS(O)(=O)=O FKOZPUORKCHONH-UHFFFAOYSA-N 0.000 description 1
- JHUFGBSGINLPOW-UHFFFAOYSA-N 3-chloro-4-(trifluoromethoxy)benzoyl cyanide Chemical compound FC(F)(F)OC1=CC=C(C(=O)C#N)C=C1Cl JHUFGBSGINLPOW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 241001589086 Bellapiscis medius Species 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Landscapes
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は優れた寸法安定性を有す
る編織物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a knitted fabric having excellent dimensional stability.
【0002】0002
【従来の技術】編織物の寸法安定性を良くするには、熱
融着性繊維を混紡させた混紡糸の使用をあげることがで
きる。従来、熱融着繊維として特公昭54−44773
号公報においては、結晶性ポリプロピレン(第一成分)
とエチレン酢酸ビニルコポリマーまたはその鹸化物及び
ポリエチレン(第二成分)をサイドバイサイドに、又は
芯鞘型に複合紡糸することにより繊維間の熱融着性,他
の異質素材との熱接着性を改善させた熱接着性複合繊維
が開示されている。BACKGROUND OF THE INVENTION In order to improve the dimensional stability of knitted fabrics, it is possible to use blended yarns in which heat-fusible fibers are blended. Previously, as a heat-fusible fiber
In the publication, crystalline polypropylene (first component)
By spinning ethylene-vinyl acetate copolymer or its saponified product and polyethylene (second component) side-by-side or in a core-sheath type, the thermal adhesion between fibers and the thermal adhesion with other different materials can be improved. A thermoadhesive composite fiber is disclosed.
【0003】アクリルやアクリル系の繊維に関しては、
紡糸時において溶融することが難しく、アクリルの熱融
着繊維は未だ開発段階である。Regarding acrylic and acrylic fibers,
Acrylic heat-sealable fibers are still in the development stage because they are difficult to melt during spinning.
【0004】また、前述の特公昭54−44773号公
報の熱融着繊維とアクリル繊維を混紡した場合、糸の染
色時該熱融着繊維は、塩基性染料で染着されず、白く残
り商品価値を著しく損なうという欠点がある。またポリ
プロピレンとポリエチレンの複合繊維であるため該繊維
に難燃性を付与することは容易でない。Furthermore, when the heat-fusible fiber of the above-mentioned Japanese Patent Publication No. 54-44773 is blended with acrylic fiber, the heat-fusible fiber is not dyed with the basic dye and remains white when dyeing the yarn. The drawback is that it significantly reduces value. Furthermore, since the fiber is a composite fiber of polypropylene and polyethylene, it is not easy to impart flame retardancy to the fiber.
【0005】[0005]
【発明が解決しようとする問題点】本発明の目的は、塩
基性染料で染色できる優れた寸法安定性を有する編織物
を提供するにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a knitted fabric that can be dyed with basic dyes and has excellent dimensional stability.
【0006】[0006]
【課題を解決するための手段】本発明は上記目的を達成
するため、以下の構成をとる。即ち、繊維表面から溶剤
を0.5〜10重量%含浸している変性アクリル繊維(
熱融着性アクリル繊維)が20%以上混紡された紡績糸
より成り、該紡績糸が50%以上使用され、実質的に均
一に編み織りされていることを特徴とする編織物である
。[Means for Solving the Problems] In order to achieve the above object, the present invention adopts the following configuration. That is, modified acrylic fibers impregnated with 0.5 to 10% by weight of solvent from the fiber surface (
This knitted fabric is made of spun yarn in which 20% or more of (thermally fusible acrylic fiber) is blended, 50% or more of the spun yarn is used, and the knitted fabric is substantially uniformly knitted.
【0007】以下、本発明の構成要件を述べる。本発明
に使用される紡績糸は、繊維表面から溶剤を0.5〜1
0重量%含浸している変性アクリル繊維(熱融着性アク
リル繊維)が20%以上混紡される。本発明の紡績糸に
使用するアクリル繊維はアクリロニトリルを主要成分と
する(40重量%以上)一般的なアクリルまたはアクリ
ル系繊維をいう。例えばカシミロン、エクスラン、ボン
ネル、ベスロン、トレロン、カネカロン等市販されてい
る通常のアクリル繊維で良い。第2コモノマーとしては
メチルアクリレート、酢酸ビニル、アクリルアミド、ア
クリル酸、塩化ビニル、塩化ビニリデン等が使用できる
。また、第3モノマーとしてはアリルスルホン酸ナトリ
ウム、メタクリルスルホン酸ナトリウム、2−アクリル
アミド2−メチルプロパンスルホン酸ナトリウム等が使
用できる。[0007] The constituent elements of the present invention will be described below. The spun yarn used in the present invention removes the solvent from the fiber surface by 0.5 to 1
20% or more of modified acrylic fiber (heat-fusible acrylic fiber) impregnated with 0% by weight is blended. The acrylic fiber used in the spun yarn of the present invention is a general acrylic or acrylic fiber containing acrylonitrile as a main component (40% by weight or more). For example, commercially available ordinary acrylic fibers such as Cashmiron, Exlan, Bonnell, Bethlon, Toleron, and Kanekalon may be used. As the second comonomer, methyl acrylate, vinyl acetate, acrylamide, acrylic acid, vinyl chloride, vinylidene chloride, etc. can be used. Further, as the third monomer, sodium allylsulfonate, sodium methacrylsulfonate, sodium 2-acrylamide 2-methylpropanesulfonate, etc. can be used.
【0008】本発明のアクリル繊維は、実質的に繊維表
面に溶剤を0.5重量%以上(対繊維重量)含浸してお
り、アクリル繊維表面に含浸された溶剤によりアクリル
繊維表面が可塑化され熱融着性が発現する。含浸してい
る溶剤が0.5重量%未満では熱融着効果が少ない。好
ましくは1重量%以上であり、特に熱融着力(解撚時の
強力)が必要な場合は、3重量%以上が好ましい。溶剤
が10重量%以上含浸させた場合、混合させる紡績用油
剤との安定性が悪くなり、スカムになったり、油剤の一
部が分離するので好ましくない。In the acrylic fiber of the present invention, the surface of the acrylic fiber is substantially impregnated with 0.5% by weight or more of a solvent (based on the weight of the fiber), and the surface of the acrylic fiber is plasticized by the solvent impregnated into the surface of the acrylic fiber. Heat fusion properties are developed. If the amount of impregnated solvent is less than 0.5% by weight, the thermal fusion effect will be low. The content is preferably 1% by weight or more, and particularly when a high thermal bonding strength (strength during untwisting) is required, the content is preferably 3% by weight or more. If the solvent is impregnated with 10% by weight or more, the stability with the spinning oil to be mixed becomes poor, resulting in scum or part of the oil separating, which is not preferable.
【0009】次に、本発明の紡績糸に使用する熱融着性
アクリル繊維の製造方法について述べる。ポリマーの重
合方法は溶液重合でも、サスペンジョン重合でも良くと
くに制限しない。紡糸する方法は湿式でも、乾式でもと
くに問題ない。使用するアクリル繊維は、原着綿,染色
後いずれであっても良い。本発明に使用する溶剤はアク
リルの一般的な有機溶剤で良く、例えばジメチルスルフ
ォキシド,ジメチルアセトアミド,ジメチルフォルムア
ミド,スルフォラン,エチレンカーボネイト等が使用で
きる。中では、沸点の高いスルフォランが好ましく、混
合溶剤として複数の溶剤を使用しても良い。溶剤は、例
えば紡績用油剤の水溶液又はエマルジョンと混合して繊
維に実質的に均一に付着させる。0.5%程度の少量の
溶剤を繊維に付着させるためには、スプレーで直接溶剤
を噴霧した後、十分に混綿する方法があるが、揮発しや
すい希釈剤、例えば水等で溶剤を希釈した後付着するほ
うが好ましい。付着する方法は浸漬法でもスプレー法で
も良く、特に限定はしないが、浸漬法が付着斑が少なく
て良い。溶剤を繊維に含浸させるため、また希釈剤を乾
燥するために溶剤を付着後、乾燥する。乾燥が進行する
と繊維表面の溶剤により繊維が膨潤すると同時に溶剤が
含浸されるが、乾燥温度が高すぎると繊維相互で接着し
てしまう。乾燥温度が80℃を越えると接着が著しくな
り好ましくない。乾燥効率が低下するが70℃以下、好
ましくは60℃以下が良い。本発明の熱融着繊維は乾燥
により軽度に膠着することがあるが、混綿前に開繊し使
用すれば良い。次に、紡績を行なうが、紡績方法は、短
繊維、セミソ毛紡績、ソ毛紡績、空気紡績、結束紡績等
一般的な方法でよいが、変性アクリル繊維と他の繊維を
均一に混紡することが好ましい。カードに投入する前に
混綿機を通し、十分に混綿することが必要で、混綿状態
が不十分であると、熱融着効果が不均一になり製品斑の
原因となる。Next, a method for producing heat-fusible acrylic fibers used in the spun yarn of the present invention will be described. The polymerization method may be solution polymerization or suspension polymerization, and is not particularly limited. There are no particular problems with the spinning method, either wet or dry. The acrylic fibers used may be either spun dyed cotton or dyed acrylic fibers. The solvent used in the present invention may be a common organic solvent for acrylic, such as dimethyl sulfoxide, dimethyl acetamide, dimethyl formamide, sulfolane, ethylene carbonate, etc. Among them, sulfolane having a high boiling point is preferred, and a plurality of solvents may be used as a mixed solvent. The solvent is mixed with, for example, an aqueous solution or emulsion of a spinning oil to substantially uniformly adhere to the fibers. In order to attach a small amount of solvent (about 0.5%) to the fibers, there is a method of spraying the solvent directly and then thoroughly mixing the cotton, but it is also possible to dilute the solvent with a diluent that easily evaporates, such as water. Post-deposition is preferred. The method of attachment may be a dipping method or a spraying method. Although not particularly limited, the dipping method is preferable because it causes less spots of adhesion. In order to impregnate the fibers with the solvent and to dry the diluent, the solvent is applied and then dried. As drying progresses, the fibers swell due to the solvent on the fiber surface and are simultaneously impregnated with the solvent, but if the drying temperature is too high, the fibers will adhere to each other. If the drying temperature exceeds 80° C., adhesion will become significant, which is not preferable. The temperature is preferably 70°C or lower, preferably 60°C or lower, although the drying efficiency decreases. Although the heat-fusible fibers of the present invention may slightly stick together when dried, they may be used by opening them before blending. Next, spinning is performed, and general methods such as short fiber spinning, semi-straight wool spinning, straight wool spinning, air spinning, and bundle spinning may be used, but modified acrylic fibers and other fibers may be uniformly blended. is preferred. It is necessary to thoroughly mix the cotton by passing it through a cotton blending machine before putting it into the card. If the cotton is not mixed sufficiently, the heat-sealing effect will be uneven and cause unevenness in the product.
【0010】本発明の紡績糸に使用する前記変性アクリ
ル繊維の混紡率は20重量%以上であり、該紡績糸を用
い編織物を製造する。仕掛ける編機,織機は通常のもの
でよく、例えば編物の場合経編みにおいては整経時交編
するよう組織を適宜選択し、緯編みにおいては供給する
糸の口数を適宜割り振り、また織物の場合は経糸と緯糸
の組織を適宜選択する等すればよい。変性アクリル繊維
混紡糸の交編織率は50%以上、好ましくは70%以上
であり、実質的に均一に交編織される。交編織率が50
%未満では寸法安定性が十分ではない。得られた編織物
はテンター式熱風乾燥機で100℃以上で30秒間以上
熱処理し、熱融着処理をする。変性アクリル繊維の混紡
率が低い場合は熱融着をより強固にするため110℃以
上、1分間以上の熱処理が好ましい。The blending ratio of the modified acrylic fibers used in the spun yarn of the present invention is 20% by weight or more, and the spun yarn is used to produce knitted fabrics. The knitting machines and looms to be set up may be ordinary ones.For example, in the case of knitting, the weave is selected appropriately so that warp knitting is alternately knitted, and in the case of weft knitting, the number of threads to be supplied is appropriately allocated, and in the case of woven fabrics, The warp and weft structures may be appropriately selected. The modified acrylic fiber blend yarn has a knitting ratio of 50% or more, preferably 70% or more, and is substantially uniformly knitted and woven. Interlaced weave ratio is 50
%, dimensional stability is not sufficient. The obtained knitted fabric is heat-treated in a tenter-type hot-air dryer at 100° C. or higher for 30 seconds or longer to undergo heat-fusion treatment. When the blending ratio of modified acrylic fibers is low, heat treatment is preferably performed at 110° C. or higher for 1 minute or longer in order to further strengthen the heat fusion bond.
【0011】[0011]
【実施例】以下、実施例によって本発明を具体的に説明
する。尚、実施例中「%」とあるのは「重量%」を意味
する。
<繊維の強伸度測定> JIS L−1015,<
紡績糸の強伸度測定> JIS L−1095,<
紡績糸の丸編み地の寸法安定性の測定> JIS
L−1018 乾燥収縮率,
<織物の寸法安定性の測定> JIS L−104
2,<編織物の燃焼性> JIS L−1091,
にそれぞれ準じて行った。試料は家庭用洗濯機による洗
濯試験法に準じて1回処理し、測定用試料とした。[Examples] The present invention will be specifically explained below with reference to Examples. In addition, "%" in the examples means "weight %". <Measurement of fiber strength and elongation> JIS L-1015, <
Measurement of strength and elongation of spun yarn> JIS L-1095, <
Measurement of dimensional stability of circular knitted fabric of spun yarn> JIS
L-1018 Drying shrinkage rate, <Measurement of dimensional stability of textiles> JIS L-104
2, <Flammability of knitted fabrics> JIS L-1091,
Each was conducted according to the following. The sample was processed once according to the washing test method using a household washing machine, and used as a sample for measurement.
【0012】実施例
市販のカネボウアクリル(アクリロニトリル90重量%
,メチルアクリレート9.5重量%,メタクリルスルホ
ネートナトリウム塩0.5重量%)3d51mmと難燃
アクリル,ルフネン(アクリロニトリル60重量%,ビ
ニリデン39重量%,メタクリルスルホネートナトリウ
ム塩1重量%)3d51mmをアクリル繊維として使用
した。アクリル繊維10grを100mlの溶剤水溶液
に表1に示す条件で浸漬処理した。浸漬法により溶剤を
繊維に付着させた後、遠心脱水機で絞り、表2に示す条
件で熱風乾燥機で乾燥した。得られた変性アクリル繊維
を表3に示す混紡率で通常のアクリル繊維と混打綿機で
ミックスし、ローラー式練条機を2回通し、フライヤー
式粗紡機で粗糸を作り、短紡績機にて撚数420回/m
で混紡し25番単糸、撚数540回/mで混紡し52番
単糸を得、52番単糸はダブルツイスターで上撚を23
0回/m掛け双糸を得た。編物用には変性アクリル繊維
の混紡糸と通常糸とを双糸にした交撚双糸も準備した。
得た単糸の強力をテンシロン型引っ張り試験機で測定し
、表3に示した。表3No.2(参考例)は変性アクリ
ル繊維の溶剤付着量が低く、No.1(参考例)は混紡
率が低く、No.4(参考例)は変性アクリル繊維の乾
燥温度が高過ぎ膠着しているため通常の紡績ができなか
った。52番双糸を経糸に25番単糸を緯糸にし、経緯
それぞれ120本、100本の平織りにした。難燃性を
試験する織物は原料アクリルにすべて前述のルフネン3
d51mmを使用した。変性アクリル繊維の混紡糸は経
緯それぞれ通常のアクリル純糸と1本飛びの平織り「織
り地No.1」と変性アクリル繊維の混紡糸は経緯それ
ぞれ2本に通常アクリル純糸1本の平織り「織り地No
.2」を作成した。参考例として対応する通常のアクリ
ル純糸で「参考織り地」を作成した。また丸編地は通常
のジャージー用32口の丸編機を使用しすべて52番交
撚双糸を使用した編地「編み地No.1」と1口飛びに
変性アクリル繊維の52番混紡双糸と52番交撚双糸を
使用した編地「編み地No.2」を作成した。参考例と
して対応する通常のアクリル純糸で「参考編み地」を作
成した。得られた編織物は110℃3分間の乾熱処理を
行った。表4に得られた編織物の寸法安定性試験結果を
示す。また同様にして難燃アクリル使用の丸編地、通常
のジャージー用32口の丸編機を使用しすべて変性アク
リル繊維52番交撚双糸を使用した編地の垂直法燃焼性
試験結果は残炎時間2秒、炭化距離5cmと優れた難燃
性を示した。寸法安定性は「編み地No.1」とほとん
ど差がなく優れていた。Example Commercially available Kanebo acrylic (acrylonitrile 90% by weight)
, methyl acrylate 9.5% by weight, methacrylsulfonate sodium salt 0.5% by weight) 3d51mm and flame-retardant acrylic, Rufunene (acrylonitrile 60% by weight, vinylidene 39% by weight, methacrylsulfonate sodium salt 1% by weight) 3d51mm as acrylic fiber. used. 10g of acrylic fiber was immersed in 100ml of an aqueous solvent solution under the conditions shown in Table 1. After the solvent was applied to the fibers by the dipping method, the fibers were squeezed using a centrifugal dehydrator and dried using a hot air dryer under the conditions shown in Table 2. The obtained modified acrylic fibers were mixed with normal acrylic fibers at the blending ratio shown in Table 3 using a cotton blending machine, passed through a roller type drawing machine twice, roving was made using a flyer type roving machine, and then passed through a short spinning machine. Number of twists: 420 times/m
Blended with No. 25 single yarn, mixed with 540 twists/m to obtain No. 52 single yarn, and No. 52 single yarn was twisted with double twister to obtain No.
A double thread was obtained by threading 0 times/m. For knitting, we also prepared intertwisted twin yarns made of a blended yarn of modified acrylic fibers and a normal yarn. The strength of the obtained single yarn was measured using a Tensilon type tensile tester, and the results are shown in Table 3. Table 3 No. No. 2 (reference example) has a low amount of solvent attached to the modified acrylic fiber. No. 1 (reference example) has a low blending ratio. In Example 4 (Reference Example), the drying temperature of the modified acrylic fibers was too high and they stuck together, so normal spinning could not be performed. The No. 52 double yarn was used as the warp yarn, and the No. 25 single yarn was used as the weft yarn, making a plain weave with 120 yarns and 100 yarns for the warp and warp, respectively. The fabrics tested for flame retardancy are all made of acrylic material and the above-mentioned Rufunen 3.
d51mm was used. The blended yarn of modified acrylic fibers is a plain weave "Weave Fabric No. 1", which has regular pure acrylic yarn and one plain weave in each warp, and the blended yarn of modified acrylic fiber is a plain weave "fabric No. 1" with one regular pure acrylic yarn in each warp and warp. Earth No.
.. 2" was created. As a reference example, a "reference woven fabric" was created using the corresponding normal acrylic pure yarn. In addition, the circular knitted fabric is made using a regular 32-hole circular knitting machine for jersey, and the fabric is ``Knitted Fabric No. 1'', which uses a No. 52 intertwisted double yarn, and the No. 52 mixed yarn of modified acrylic fiber in each stitch. A knitted fabric “Knitted Fabric No. 2” was created using yarn and No. 52 intertwisted twin yarn. As a reference example, a "reference knitted fabric" was created using the corresponding normal acrylic pure yarn. The obtained knitted fabric was subjected to dry heat treatment at 110° C. for 3 minutes. Table 4 shows the dimensional stability test results of the obtained knitted fabric. Similarly, the vertical flammability test results of a circular knitted fabric using flame-retardant acrylic and a fabric knitted with modified acrylic fiber No. 52 twisted double yarn using a regular 32-neck circular knitting machine for jersey are still available. It exhibited excellent flame retardancy with a flame time of 2 seconds and a carbonization distance of 5 cm. The dimensional stability was excellent with almost no difference from "knitted fabric No. 1".
【0013】[0013]
【表1】[Table 1]
【0014】[0014]
【表2】[Table 2]
【0015】[0015]
【表3】[Table 3]
【0016】[0016]
【表4】[Table 4]
【0017】[0017]
【発明の効果】本発明の変性アクリル繊維を混紡した紡
績糸を使用した編織物は優れた寸法安定性を示す。[Effects of the Invention] The knitted fabric using the spun yarn blended with the modified acrylic fiber of the present invention exhibits excellent dimensional stability.
Claims (1)
%含浸している変性アクリル繊維が20%以上混紡され
た紡績糸より成り、該紡績糸が50%以上使用され、実
質的に均一に交編織されていることを特徴とする編織物
。Claim 1: Consisting of a spun yarn in which 20% or more of modified acrylic fibers are impregnated with 0.5 to 10% by weight of a solvent from the fiber surface, 50% or more of the spun yarn is used, and the yarn is substantially uniform. A knitted fabric characterized by being mixed and woven.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7254491A JPH04281051A (en) | 1991-03-11 | 1991-03-11 | Knitted fabric excellent in dimensional stability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7254491A JPH04281051A (en) | 1991-03-11 | 1991-03-11 | Knitted fabric excellent in dimensional stability |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04281051A true JPH04281051A (en) | 1992-10-06 |
Family
ID=13492409
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7254491A Pending JPH04281051A (en) | 1991-03-11 | 1991-03-11 | Knitted fabric excellent in dimensional stability |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04281051A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016158774A1 (en) * | 2015-03-31 | 2016-10-06 | 株式会社カネカ | Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same |
-
1991
- 1991-03-11 JP JP7254491A patent/JPH04281051A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016158774A1 (en) * | 2015-03-31 | 2016-10-06 | 株式会社カネカ | Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same |
US10787558B2 (en) | 2015-03-31 | 2020-09-29 | Kaneka Corporation | Thermoplastic modacrylic resin composition, method for manufacturing same, molded article of same, and acrylic fibers and method for manufacturing same |
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