JPH07102475A - Production of antifungal and flame-retardant textile product - Google Patents
Production of antifungal and flame-retardant textile productInfo
- Publication number
- JPH07102475A JPH07102475A JP27882593A JP27882593A JPH07102475A JP H07102475 A JPH07102475 A JP H07102475A JP 27882593 A JP27882593 A JP 27882593A JP 27882593 A JP27882593 A JP 27882593A JP H07102475 A JPH07102475 A JP H07102475A
- Authority
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- Japan
- Prior art keywords
- flame
- fibers
- retardant
- antifungal
- textile product
- 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.)
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- Chemical Or Physical Treatment Of Fibers (AREA)
- Artificial Filaments (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、難燃性繊維製品の難燃
性を損うことなく抗菌性を付与する方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for imparting antibacterial properties to a flame-retardant fiber product without impairing the flame retardancy.
【0002】[0002]
【従来の技術】現在市販されている難燃性有機繊維は、
繊維中もしくは繊維表面上に燐系,窒素系,硫黄系等の
有機難燃剤を付与したものであり、難燃効果はあるが、
これに通常の有機化合物系の抗菌剤を用いて、抗菌,抗
かび加工をしたり、それに伴う樹脂加工を施すと、繊維
の難燃性が低下する欠点がある。2. Description of the Related Art The flame-retardant organic fibers currently on the market are
An organic flame retardant such as a phosphorus-based, nitrogen-based, or sulfur-based flame retardant is added to the fiber or on the surface of the fiber.
If a conventional organic compound-based antibacterial agent is used for antibacterial and antifungal treatments or resin treatments associated therewith, the flame retardancy of the fiber is lowered.
【0003】一方、最近、繊維製品に恒久的な抗菌性を
付与する要望が高まりつつある。もちろん、日常生活に
も繊維製品が抗菌性であることは重要であるが、特に最
近必要性が増しているのが、病院,療養所,老人ホーム
等に使用するカーテン,ベッドシーツ,ふとん等の繊維
製品である。On the other hand, recently, there is an increasing demand for imparting a permanent antibacterial property to textile products. Of course, it is important for textiles to have antibacterial properties in daily life, but there is an increasing need in recent years for curtains, bed sheets, futons, etc. used in hospitals, nursing homes, nursing homes, etc. It is a textile product.
【0004】これらの療養施設に使用する繊維製品は、
施設の性格上、不燃性もしくは難燃性であることが義務
づけられているが、これに加えてMRSA(耐性菌)、
即ち、抗生物質が効果を示さない細菌の蔓延防止が重要
な社会問題となりつつある。The textile products used in these medical facilities are
Due to the nature of the facility, it is required to be non-combustible or flame-retardant. In addition to this, MRSA (resistant bacteria),
That is, prevention of the spread of bacteria against which antibiotics are not effective is becoming an important social problem.
【0005】従来、抗菌剤としては抗生物質が多用され
ていたが、MRSAの蔓延によって、抗生物質のみに頼
ることはできず、殺菌剤による洗浄,手洗いの勵行等の
対策はとられているが、カーテン,ベッドシーツ等の繊
維製品自体にも抗菌性を持たせる要望が高まりつつあ
る。Conventionally, antibiotics have been widely used as antibacterial agents, but due to the prevalence of MRSA, it is not possible to rely on antibiotics alone, and measures such as cleaning with bactericides and hand washing are taken. However, there is an increasing demand for textile products such as curtains and bed sheets to have antibacterial properties.
【0006】MRSAに対しては水銀,錫,銅,銀等の
化合物、即ち無機化合物が殺菌効果を示す。しかし、水
銀化合物は猛毒であって、使用が禁止されており、錫化
合物も毒性が強くて使用が困難である。Compounds such as mercury, tin, copper, and silver, that is, inorganic compounds have a bactericidal effect on MRSA. However, mercury compounds are extremely poisonous and their use is prohibited, and tin compounds are also highly toxic and difficult to use.
【0007】銅,銀等の化合物が毒性は比較的少くて好
適であるので、これらを使用することも提案されている
が、樹脂によって繊維表面に固着する方法をとると、こ
れらの抗菌剤は、多くの場合、固着用の樹脂に包埋さ
れ、樹脂によっては、該抗菌剤と反応してその効果を充
分に発揮することができない。また着色するのも難点の
ひとつである。Since compounds such as copper and silver are suitable because they have relatively low toxicity, it is proposed to use them. However, when they are fixed to the fiber surface with a resin, these antibacterial agents are In many cases, it is embedded in a fixing resin, and depending on the resin, it may not react sufficiently with the antibacterial agent to exert its effect sufficiently. Also, coloring is one of the difficulties.
【0008】この欠点を補うために銀化合物,銅化合物
をゼオライト等の吸着剤に吸着させて、これを繊維製品
に固着する方法が開発されている。この場合には、ゼオ
ライトが樹脂に包埋されても比較的銀イオン,銅イオン
は移動しやすいので、抗菌性は発揮されるが、光によ
り、または空気中の硫化物等と反応して黄変,褐変等を
起こす欠点がある。In order to compensate for this drawback, a method has been developed in which a silver compound or a copper compound is adsorbed on an adsorbent such as zeolite, and the adsorbent is fixed to a fiber product. In this case, even if the zeolite is embedded in the resin, silver ions and copper ions are relatively easy to move, so that the antibacterial property is exhibited, but yellow light is caused by light or by reacting with sulfides in the air. It has the drawback of causing discoloration and browning.
【0009】[0009]
【発明が解決しようとする課題】本発明は、前述したよ
うな問題点があるにもかかわらず、難燃性を損うことな
く、優れた抗菌性を有する繊維製品を製造することを目
的とする。SUMMARY OF THE INVENTION The present invention has an object of producing a fiber product having excellent antibacterial properties without impairing flame retardancy in spite of the above-mentioned problems. To do.
【0010】即ち、本発明は、繊維中に燐系,窒素系,
硫黄系等の有機難燃剤を含有する難燃性繊維に酸化亜鉛
または酸化亜鉛を主体とするセラミック粉末を付与する
ことを特徴とするものである。That is, according to the present invention, phosphorus-based, nitrogen-based,
It is characterized in that zinc oxide or a ceramic powder mainly composed of zinc oxide is applied to flame-retardant fibers containing an organic flame retardant such as sulfur.
【0011】更に本発明の方法により得られた繊維製品
は、太陽光線,紫外線,可視光線,赤外線,熱線等の輻
射線に対する遮断性が優れ、風合,白度とも良好であ
り、衣料用として日焼けを防ぎ、涼しい繊維製品を得る
こともできる。Further, the textile product obtained by the method of the present invention has an excellent shielding property against radiant rays such as sun rays, ultraviolet rays, visible rays, infrared rays, and heat rays, and has a good texture and whiteness. It can also prevent sunburn and obtain cool textile products.
【0012】本発明に使用する繊維には、有機難燃剤を
含有するポリエステル、ポリアミド、ポリオレフィン等
の溶融紡糸繊維、ポリアクリロニトリル系、レーヨン系
等の湿式紡糸繊維、アセテート等の乾式紡糸繊維等が挙
げられる。The fibers used in the present invention include melt-spun fibers such as polyester, polyamide, and polyolefin containing organic flame retardant, wet-spun fibers such as polyacrylonitrile-based and rayon-based, and dry-spun fibers such as acetate. To be
【0013】また本発明に使用される酸化亜鉛は、これ
単独もしくは、酸化亜鉛を50重量%以上含み、これ以
外にも酸化チタン,酸化ジルコニウム,酸化アルミニウ
ム等が混合されたセラミックスであってもよい(総称し
て酸化亜鉛系セラミックスという)。粒子径は、3μm
以下、好ましくは1μm以下まで微粉砕するか、分級し
たものを用いるのが懸濁液が安定になるので好ましい。The zinc oxide used in the present invention may be ceramics alone or containing 50% by weight or more of zinc oxide and other than these, titanium oxide, zirconium oxide, aluminum oxide and the like are mixed. (Generally referred to as zinc oxide ceramics). Particle size is 3 μm
Hereafter, it is preferable to use finely pulverized or classified particles of preferably 1 μm or less because the suspension becomes stable.
【0014】上記酸化亜鉛系セラミックスは、繊維,
糸,織物,編物等の繊維製品に、バインダーとなるべき
樹脂とともに懸濁液の状態としてパディング,コーティ
ング,プリント,スプレイ等の後加工手段によって施
す。The zinc oxide-based ceramics are fibers,
Textile products such as yarns, woven fabrics, and knits are applied as a suspension together with a resin serving as a binder by post-processing means such as padding, coating, printing and spraying.
【0015】酸化亜鉛系セラミックスを繊維製品に付与
する量は、繊維製品に対して0.1〜40重量、好まし
くは0.5〜30重量%がよい。The amount of zinc oxide ceramics applied to the fiber product is 0.1 to 40% by weight, preferably 0.5 to 30% by weight, based on the fiber product.
【0016】使用される樹脂としては、尿素ホルマリン
系,メラミンホルマリン系等の熱硬化性樹脂,ポリエス
テル系,ポリ酢酸ビニル系,ポリアクリル酸エステル
系,ポリアミド系等の熱可塑性樹脂,あるいはこれらの
樹脂の併用があるが、難燃性を阻害しないように、でき
るだけ熱可塑性樹脂を主体として使用するのが好適であ
る。特にポリエステル系繊維製品に対しては熱可塑性ポ
リエステル系樹脂の使用が好ましい。Examples of the resin used include thermosetting resins such as urea formalin type and melamine formalin type, thermoplastic resins such as polyester type, polyvinyl acetate type, polyacrylic acid ester type, polyamide type, or the like. However, it is preferable to use a thermoplastic resin as a main component as much as possible so as not to impair the flame retardancy. Particularly for polyester fiber products, it is preferable to use a thermoplastic polyester resin.
【0017】この繊維製品に形成される樹脂層は、それ
自体が難燃性であることが好ましいが、該樹脂層が難燃
性でない場合は、難燃剤、例えば三酸化アンチモン,五
酸化アンチモンの無機系難燃剤,燐系有機難燃剤等を酸
化亜鉛系セラミックスの懸濁液に添加して、樹脂層に難
燃性を付与してもよい。The resin layer formed on the fiber product is preferably flame-retardant itself, but when the resin layer is not flame-retardant, a flame retardant such as antimony trioxide or antimony pentoxide is used. Inorganic flame retardants, phosphorus organic flame retardants, etc. may be added to the zinc oxide ceramic suspension to impart flame retardancy to the resin layer.
【0018】固着処理は、通常の繊維製品の樹脂加工と
同様に樹脂含浸,搾液,乾燥,熱処理の工程を経るのが
一般的であるが、この方法に限定されるものではなく、
前述したようにスプレー等によって付与したあと、乾
燥,熱処理してもよい。The fixing treatment generally involves the steps of resin impregnation, squeezing, drying, and heat treatment as in the case of resin processing of ordinary textiles, but it is not limited to this method.
As described above, it may be applied by spraying or the like, and then dried and heat-treated.
【0019】次に本発明を実施例について更に詳細に説
明する。Next, the present invention will be described in more detail with reference to Examples.
【0020】[0020]
実施例1 有機燐化合物を添加した難燃性ポリエステル(東洋紡績
社製“ハイム”)フィラメント(75P/48F)のト
リコット編地からなるカーテン用布帛地をトリポリ燐酸
ソーダ0.5g/l、非イオン系界面活性剤2g/lの
精練浴で精練後、次の処方の浴で加工し、難燃性を調べ
るとともに抗菌,防かび効果を試験した。Example 1 A cloth for a curtain made of a tricot knitted fabric of a flame-retardant polyester (“Heim” manufactured by Toyobo Co., Ltd.) filament (75P / 48F) to which an organic phosphorus compound was added was used, and 0.5 g / l of sodium tripolyphosphate and nonionic were used. After scouring with a scouring bath containing 2 g / l of a surface-active agent, it was processed with a bath having the following formulation to examine flame retardancy and test antibacterial and antifungal effects.
【0021】処方 超微粒子酸化亜鉛粉末 2重量% 難燃性ポリエステルエマルジョン 3重量% (高松油脂社製TKセット43) 三酸化アンチモン粉末 3重量% 水 残部 懸濁液に調製Formulation Ultrafine zinc oxide powder 2% by weight Flame-retardant polyester emulsion 3% by weight (TK Set 43 manufactured by Takamatsu Yushi Co., Ltd.) Antimony trioxide powder 3% by weight Water balance Prepared as a suspension
【0022】上記処方の処理浴で、上記カーテン用布帛
地をパッディング処理し、絞り率80%で絞り、130
℃で熱風乾燥し、160℃で1分間熱処理した。The curtain fabric was padded with the treatment bath of the above formulation and squeezed at a drawing rate of 80% to obtain 130
It was dried with hot air at ℃ and heat-treated at 160 ℃ for 1 minute.
【0023】処理後のカーテン用布帛地について洗濯
前,洗濯後について各5点のサンプルを採取し、防炎性
をテストしたところ、いずれも残炎時間2〜3秒,残じ
ん時間3〜4.5秒,炭化面積20〜27cm2,炭化
長(たるませた場合)15〜19cmとなり、いずれも
自治省消防法防炎性能基準に合格するものであった。The curtain fabric after the treatment was sampled at 5 points each before and after the washing, and the flameproofness was tested. In both cases, the afterflame time was 2 to 3 seconds and the dust time was 3 to 4 The carbonization area was 0.5 seconds, the carbonization area was 20 to 27 cm 2 , and the carbonization length (when slackened) was 15 to 19 cm, all of which passed the Ministry of Internal Affairs and Communications Fire Defense Law flameproof performance standard.
【0024】なお、難燃性試験は、自治省消防法防炎性
能基準(JISL−1091,A−1法)に基づいて行
った。The flame retardancy test was conducted based on the Ministry of Internal Affairs and Communications Fire Defense Law flameproof performance standard (JISL-1091, A-1 method).
【0025】次に上記処理布の抗菌防かび性試験を行っ
た。試験法は繊維製品衛生加工協議会の制定した「衛生
加工製品の加工効果評価試験方法」の「シェークフラス
コ法」に従って行った。Next, an antibacterial and antifungal test of the treated cloth was conducted. The test method was performed according to the "Shake flask method" of "Testing method for processing effect evaluation of sanitary processed products" established by the Textile Products Sanitary Processing Council.
【0026】即ち、まず培養した菌懸濁液(使用菌株:
クレブシエラ ニューモニエATCC4352)をリン
酸緩衝液で1000倍に希釈し、試験菌液を調製する。
湿熱滅菌された三角フラスコにサンプル及び該試験菌液
を加えて、生菌数を測定する〔A〕。That is, first, a cultivated bacterial suspension (used strain:
Klebsiella pneumoniae ATCC 4352) is diluted 1000-fold with a phosphate buffer to prepare a test bacterial solution.
The sample and the test bacterial solution are added to an Erlenmeyer flask that has been sterilized by heat and humidity, and the viable cell count is measured [A].
【0027】次いで三角フラスコを1時間振とうしたの
ち、その生菌数を測定する〔B〕。Then, the Erlenmeyer flask is shaken for 1 hour, and the number of viable bacteria is measured [B].
【0028】滅菌率の算出は次の式により求めた。 The sterilization rate was calculated by the following formula.
【0029】試験の結果は、未洗濯布で滅菌率99.9
%以上,洗濯5回(F−1法)後で滅菌率98%以上で
あり、洗濯後も優れた抗菌性を示した。またこのサンプ
ルは6ケ月経過後も同様の試験で滅菌率98%以上を示
した。更にこのサンプルは6ケ月経過後も黄変を起こす
こともなかった。The result of the test is that the sterilization rate of unwashed cloth is 99.9.
%, The sterilization rate was 98% or more after 5 times of washing (F-1 method), and excellent antibacterial properties were shown even after washing. Also, this sample showed a sterilization rate of 98% or more in the same test even after 6 months. Furthermore, this sample did not cause yellowing even after 6 months.
【0030】[0030]
【実施例2】難燃性ポリエステル(東洋紡績社製“ハイ
ム”)短繊維綿(1.5D,20mm)からなる80g
/m2の不織布用ウエブを次の処方で抗菌防黴加工を行
った。Example 2 80 g of flame-retardant polyester (“Heim” manufactured by Toyobo Co., Ltd.) short fiber cotton (1.5 D, 20 mm)
A non-woven fabric web of / m 2 was subjected to antibacterial and antifungal treatment with the following formulation.
【0031】処方 超微粒子酸化亜鉛粉末 2重量% 難燃性ポリエステルエマルジョン 3重量% (高松油脂社製TKセット413) 水 残部 懸濁液に調製Prescription Ultrafine zinc oxide powder 2% by weight Flame-retardant polyester emulsion 3% by weight (TK set 413, manufactured by Takamatsu Yushi Co., Ltd.) Water balance Prepared as a suspension
【0032】上記不織布用ウエブを上記処方の処理浴で
パッディング処理し、100%に絞り、130℃で乾燥
した後、160℃で2分間熱処理した。The non-woven fabric web was padded in the treatment bath of the above formulation, squeezed to 100%, dried at 130 ° C., and then heat treated at 160 ° C. for 2 minutes.
【0033】処理された不織布について、実施例1と同
様の方法で防炎性テストをしたところ、各試料とも残炎
時間2〜2.5秒,残じん時間3〜4.5秒,炭化面積
20〜26cm2,炭化長15〜17cmの結果が得ら
れ、いずれも自治省消防法防炎性能基準に合格した。The treated nonwoven fabric was subjected to a flameproofness test in the same manner as in Example 1. Each sample had an afterflame time of 2 to 2.5 seconds, a dust time of 3 to 4.5 seconds, and a carbonization area. The results of 20 to 26 cm 2 and carbonization length of 15 to 17 cm were obtained, and all passed the Ministry of Internal Affairs and Communications Fire Act Fire Prevention Performance Standards.
【0034】また抗菌防かび性能試験では、不織布ウエ
ブは未洗濯時で滅菌率99.9%以上,洗濯(F−1
法)5回後で滅菌率97%以上の優れた結果を得た。6
ケ月経過後もこの結果はほとんど変わらなかった。In the antibacterial and antifungal performance test, the non-woven web was sterilized at a rate of 99.9% or more before being washed (F-1
Method) After 5 times, excellent results with a sterilization rate of 97% or more were obtained. 6
This result remained almost unchanged even after the lapse of months.
【0035】[0035]
【比較例1】実施例1で使用した難燃性ポリエステルフ
ィラメント製トリコット編地からなるカーテン用布帛地
を精練後、アンモニウム塩含有シリコン系樹脂(高松油
脂社製“SX−60”,抗菌防かび加工剤)の2重量%
処理浴でパッディング処理を行い、絞り率80%で絞
り、130℃で熱風乾燥し、160℃で1分間熱処理し
た。[Comparative Example 1] After the curtain fabric made of the tricot knitted fabric made of the flame-retardant polyester filament used in Example 1 was scoured, an ammonium salt-containing silicone resin ("SX-60" manufactured by Takamatsu Yushi Co., Ltd., antibacterial and antifungal) was used. 2% by weight of processing agent)
A padding process was performed in the treatment bath, the squeezing ratio was 80%, the squeezing ratio was 80%, the film was dried with hot air at 130 ° C., and a heat treatment was performed at 160 ° C. for 1 minute.
【0036】処理後の布帛地を実施例1と同様の方法で
防炎性テストをしたところ、洗濯前,洗濯後とも残炎時
間4〜4.5秒,残じん時間5.5秒以上,炭化長25
cm〜40cm,炭化面積35〜45cmとなり、いず
れも自治省消防法防炎性能基準に合格しなかった。The treated fabric was subjected to a flameproof test in the same manner as in Example 1. As a result, the afterflame time was 4 to 4.5 seconds, and the dust time was 5.5 seconds or more before and after washing. Carbonization length 25
cm to 40 cm, carbonized area 35 to 45 cm, and none of them passed the Ministry of Internal Affairs and Communications Fire Act flameproof performance standard.
【0037】[0037]
【比較例2】実施例2で使用した難燃性ポリエステル短
繊維綿からなる不織布用ウエブをアンモニウム塩含有シ
リコン系樹脂(高松油脂社製“SX−60”,抗菌防黴
加工剤)を3重量%含むアクリル酸エステル系樹脂バイ
ンダー(カネボーNSC社製,“ヨドゾールA−2
3”)の30重量%の処理浴でパッディング処理し、1
00%に絞り、130℃で乾燥した後、160℃で2分
間熱処理した。[Comparative Example 2] A non-woven fabric web made of flame-retardant polyester short-fiber cotton used in Example 2 was treated with 3 parts by weight of an ammonium salt-containing silicone resin ("SX-60" manufactured by Takamatsu Oil & Fat Co., an antibacterial and antifungal agent). % Acrylic ester resin binder (Kanebo NSC, "Iodosol A-2"
3 ") padded with 30% by weight treatment bath, 1
It was squeezed to 00%, dried at 130 ° C., and then heat-treated at 160 ° C. for 2 minutes.
【0038】得られた不織布を実施例1と同じ方法で防
炎性テストをしたところ、残炎時間4秒以上,残じん時
間5.5秒以上,炭化長25〜40cm,炭化面積40
〜50cm2,炭化長25〜40cmとなり、いずれも
自治省消防法防炎性能基準に合格しなかった。The obtained non-woven fabric was tested for flameproofness in the same manner as in Example 1. The afterflame time was 4 seconds or longer, the dust time was 5.5 seconds or longer, the carbonization length was 25 to 40 cm, and the carbonization area was 40.
The carbonization length was ˜50 cm 2 and the carbonization length was 25 to 40 cm, and none of them passed the fire prevention performance standard of the Fire Service Law of the Ministry of Home Affairs.
【0039】[0039]
【効果】これまで説明したように、本発明の方法に繊維
製品は、本来の難燃性を低下させることなく、高い抗菌
性を示し、長期間にわたってその効果を持続させること
ができ、かつ変色することがない特徴があり、病院,食
品工場等で使用するカーテン,シーツ等にその用途は広
い。[Effect] As described above, the textile product according to the method of the present invention exhibits high antibacterial properties without deteriorating the original flame retardancy, can maintain its effect for a long period of time, and is discolored. There is a feature that does not occur, and its application is wide for curtains, sheets, etc. used in hospitals, food factories, etc.
Claims (1)
難燃剤を含有する難燃性繊維に酸化亜鉛または酸化亜鉛
を主体とするセラミック粉末を付与することを特徴とす
る抗菌性かつ難燃性繊維製品の製造法。1. An antibacterial property, characterized in that zinc oxide or a ceramic powder mainly composed of zinc oxide is applied to flame-retardant fibers containing phosphorus-based, nitrogen-based, sulfur-based, etc. organic flame retardants in the fibers. And a method of manufacturing flame-retardant textile products.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27882593A JPH07102475A (en) | 1993-10-01 | 1993-10-01 | Production of antifungal and flame-retardant textile product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27882593A JPH07102475A (en) | 1993-10-01 | 1993-10-01 | Production of antifungal and flame-retardant textile product |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07102475A true JPH07102475A (en) | 1995-04-18 |
Family
ID=17602685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27882593A Pending JPH07102475A (en) | 1993-10-01 | 1993-10-01 | Production of antifungal and flame-retardant textile product |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07102475A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2309461A (en) * | 1996-01-23 | 1997-07-30 | Courtaulds Fibres | Manufacture of acrylic fibre |
| EP0980922A3 (en) * | 1998-08-05 | 2001-06-27 | Eva-Maria Haug | Fiber fabric |
| FR2851581A1 (en) * | 2003-02-21 | 2004-08-27 | Rhodianyl | Flame retardant thermoplastic yarns, fibers and/or filaments, obtained by deposition of flame retardant, e.g. phosphorus compound, while being transported during production and/or treatment |
| CN103194885A (en) * | 2013-04-19 | 2013-07-10 | 中国民航大学 | Method for microwave synthesis of nano-ZnO assembled cotton fibers |
| CN107299405A (en) * | 2017-08-14 | 2017-10-27 | 恒天海龙(潍坊)新材料有限责任公司 | A kind of preparation method of hollow speed heat warm-keeping cellulose fiber |
-
1993
- 1993-10-01 JP JP27882593A patent/JPH07102475A/en active Pending
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2309461A (en) * | 1996-01-23 | 1997-07-30 | Courtaulds Fibres | Manufacture of acrylic fibre |
| GB2309461B (en) * | 1996-01-23 | 1999-10-20 | Courtaulds Fibres | Manufacture of acrylic fibre |
| EP0980922A3 (en) * | 1998-08-05 | 2001-06-27 | Eva-Maria Haug | Fiber fabric |
| FR2851581A1 (en) * | 2003-02-21 | 2004-08-27 | Rhodianyl | Flame retardant thermoplastic yarns, fibers and/or filaments, obtained by deposition of flame retardant, e.g. phosphorus compound, while being transported during production and/or treatment |
| WO2004079080A1 (en) * | 2003-02-21 | 2004-09-16 | Rhodianyl | Fire-resistant threads, fibres, filaments and textile articles |
| CN103194885A (en) * | 2013-04-19 | 2013-07-10 | 中国民航大学 | Method for microwave synthesis of nano-ZnO assembled cotton fibers |
| CN107299405A (en) * | 2017-08-14 | 2017-10-27 | 恒天海龙(潍坊)新材料有限责任公司 | A kind of preparation method of hollow speed heat warm-keeping cellulose fiber |
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