JPH0351802B2 - - Google Patents
Info
- Publication number
- JPH0351802B2 JPH0351802B2 JP59191242A JP19124284A JPH0351802B2 JP H0351802 B2 JPH0351802 B2 JP H0351802B2 JP 59191242 A JP59191242 A JP 59191242A JP 19124284 A JP19124284 A JP 19124284A JP H0351802 B2 JPH0351802 B2 JP H0351802B2
- Authority
- JP
- Japan
- Prior art keywords
- antistatic
- yarn
- dust
- floating
- fabric
- 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.)
- Expired - Lifetime
Links
- 239000004744 fabric Substances 0.000 claims description 28
- 239000000835 fiber Substances 0.000 claims description 28
- 239000002216 antistatic agent Substances 0.000 claims description 17
- 229920000728 polyester Polymers 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 239000002759 woven fabric Substances 0.000 claims description 4
- 229920001281 polyalkylene Polymers 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 150000004812 organic fluorine compounds Chemical class 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 230000002829 reductive effect Effects 0.000 claims description 2
- 150000003377 silicon compounds Chemical class 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims 1
- 239000000428 dust Substances 0.000 description 18
- 239000002245 particle Substances 0.000 description 8
- 230000035699 permeability Effects 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 230000003068 static effect Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- -1 Polyethylene terephthalate Polymers 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 239000002923 metal particle Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 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
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011817 metal compound particle Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
Landscapes
- Professional, Industrial, Or Sporting Protective Garments (AREA)
- Woven Fabrics (AREA)
Description
産業上の利用分野
本発明は防塵衣に関する。精密工業、半導体、
医薬品、食品などの製造工程において、又病院や
微生物を取扱う分野において所謂クリーンルーム
がめざましく発展しており、これらのクリーンル
ーム内の作業衣として防塵性の優れた衣服が必要
とされているが本発明はその防塵衣に関するもの
である。
従来の技術
防塵衣の必要な性能としては、(イ)塵通過阻止能
が高いこと。(ロ)塵が付着し難く落易いこと、(ハ)発
塵性が低いこと、(ニ)制電性が優れていること、(ホ)
耐薬品性に優れていることなど総合的な性能が要
求される。防塵衣に用いられる素材としては、例
えば特開昭55−30436号実施例に見るようにポリ
エチレンテレフタレートが多いが、制電性の見地
からは不満足なものである。
発明が解決しようとする問題点
制電性の見地からは、制電剤を混合した制電ポ
リエステル繊維を用いることが好ましい。しか
し、一般にポリエステルに耐摩耗性が不充分で摩
擦によつて切断したりフイブリル化し、それ自体
が発塵する傾向があるが、この傾向は制電剤を混
合した制電ポリエステル繊維において更に著し
い。すなわち制電性と防塵性とは相反する性格が
ある。
本発明の目的は制電性及び発塵性が共にすぐれ
た改善された防塵衣を提供することにある。
問題を解決するための手段
本発明の防塵衣は、(イ)布地がポリエステル連続
フイラメント平織物からなり、(ロ)該平織物は経糸
及び緯糸の1方が浮き(浮糸)、他方が沈む(沈
糸)構造を有し、且つ(ハ)沈糸は制電剤を混合され
た制電繊維であり、浮糸は非制電繊維であること
を特徴とする。
ここでポリエステルは特に限定されないが、例
えばポリエチレンテレフタレート(以下PETと
記す)、ポリブチレンテレフタレート(以下PBT
と記す)、それらに少量(51%以下、特に10%以
下)の第3成分を共重合又は混合した変性体が好
適である。
織組織は平織でなければならない。防塵衣用の
布は、埃通過阻止の観点から空隙の少ない組織を
必要とする。空隙の量は通気度で評価し得る。通
気度はJIS L−1096(1979)A法(フラジール法)
によつて測定する。綾織物では通気度は通常20
ml/cm3/秒以上であるが、緻密な平織物では10
ml/cm3/秒以下とすることが容易である。通気度
は10ml/cm3/秒以下が好ましく、5ml/cm3/秒以
下が特に好ましく、2ml/cm3/秒が最も好まし
い。しかしながら通気度が小さすぎると着用感が
劣るので、0.1ml/cm3/秒以上、特に0.3ml/cm3/
秒以上が好ましい。通気度の低い布は細い繊維
(例えば単糸3d以下、特に0.1〜2d)を高密度で製
織したり、高い収縮率(例えば面積収縮率10%以
上、特に20〜50%)で収縮することにより得られ
る。更に必要があればカレンダー加工等で布を押
圧して緻密化することが出来る。平織物の別の特
長は表面が平滑で埃の付着性が低いこと、耐摩耗
性及び摩擦帯電性が優れていることにある。
制電繊維に混合する制電剤としては、ポリエチ
レンオキシドなどのポリアルキレンエーテル及び
その誘導体、共重合体(例えばエーテル/エステ
ルブロツク共重合体)が好適であり、更にそれら
に水酸基、アミノ基、カルボキシル基、スルホン
基及びそれらの金属塩等の極性基を導入したり、
極性基を有する有機化合物を混用(併用)するこ
とも好ましい。混合構造としては、制電剤がポリ
エステル(マトリクス)中に微細な粒子状(多く
の場合針状粒子)で分散されている流状混合も用
いられるが、本発明者等が特公昭47−49766号公
報に開示したような、繊維横断面では制電剤が微
細な多数の点状(星雲状)に分散し、長さ方向に
は実質的に連続した線状の構造を有するものが制
電性に優れ、従つて少量の混合率で充分な制電性
が得られるので最も好ましい。例えばポリエチレ
ンオキシド系の非イオンポリマーの場合1〜5%
程度、それにアルキルベンゼンスルホン酸ソーダ
等のイオン性化合物を10〜20%混用した場合は
0.1〜2%程度、すなわち粒状混合に較べて1/2〜
1/10程度の混合率で優れた制電性が得られる。
しかしながら、制電剤を混合したポリエステル
繊維は、未混合品に較べて摩擦等によつてフイブ
リル化し発塵の原因となる傾向がやゝ強い。この
傾向は制電剤の混合率が大きいほど強い(従つて
連続線状混合が好ましい)。いずれにせよ制電繊
維は摩耗に対する抵抗性がやゝ劣る場合が多いの
で、沈み糸に用い、浮糸は耐摩耗性の優れた非制
電糸を用いる。
第1図は本発明に用いる平織の斜視説明図であ
る。図において1は浮糸であり2は沈糸である。
第2図は第1図織物の浮糸1方向の断面図であ
り、第3図は沈糸2方向の断面図である。第2図
において点線10〜10′は浮糸の表面であり、
点線20−20′は沈糸の表面である。面10−
10′と面20−20′との距離Aを「浮き高さ」
と記す。
一般に平織は経糸と緯糸の一方が沈み他方が浮
く構造ではなく、Aは零に近い場合が多い。しか
し織織時の張力及び経糸と緯糸の太さ(硬さ)な
どを変えて、浮き高さAを10μm以上、特に20〜
100μmとすることが出来、沈糸が外部の物体と
接触し損傷する確率を大巾に低減することが出来
る。すなわち経糸又は緯糸の1方の製織時の張力
を大きくすることにより、それを沈糸とすること
が出来る。同様に一方の糸を他方より多く収縮さ
せることにより、或いはより太く(硬く)するこ
とによりそれを沈み糸とすることが出来る。更に
上記3つの方法(高張力、高収縮、太糸)の2つ
以上を組合せて一層浮き高さを大きくすることが
出来る。
浮糸は非制電ポリエステル繊維である。浮糸は
耐摩耗性の優れていることが望ましい。例えば、
PET、PBTなどのホモポリマーの他、それらに
第3成分を共重合したり、混合して摩擦係数を低
減させたり、耐摩耗性を改善したものが好まし
い。摩擦係数(例えば対金属摩擦係数)を低減さ
せる成分としては、パラフイン、ポリオレフイ
ン、ポリアルキレンエーテル、アルキル基を有す
る化合物、有機シリコン化合物(例えばポリオル
ガノシロキサンなど)、有機弗素化合物(例えば
ポリ弗化エチレン誘導体その他)などの1種又は
2種以上の併用があげられる。混合率は0.001〜
10%程度、特に0.1〜5%が好適なことが多い。
布地は制電性でなければならない。制電ポリエ
ステル繊維を緯糸に用いた織物はかなり優れた制
電性を有するが、更に高度の制電性が必要な場合
は導電性繊維を併用することが出来る。導電性繊
維としては金属繊維、金属メツキ繊維、金属化合
物(半導体など)その他の導電性物質(比抵抗
107Ω・cm以下)からなる導電層を表面や内部に
有する繊維、導電性粒子又は高い導電性を有する
成分を混合した樹脂からなる導電層を表面又は内
部に有する繊維などがあげられる。導電性粒子と
しては、カーボンブラツク、金属粒子、金属化合
物粒子、金属又は金属化合物の薄層を表面に有す
る粒子などがあげられる。中でも導電性粒子を含
む導電層と繊維形成性のポリマーからなる保護層
とが接合された複合繊維が最も好適である。導電
性繊維の長さ1cm当りの電気抵抗は1011Ω以下が
好ましく、108Ω以下が最も好ましい。
導電性繊維は、制電性繊維又は非制電性繊維と
合糸又は合撚して、緯糸又は/及び経糸に例えば
一定間隔で交編することが出来る。導電性繊維の
制電効果は、コロナ放電による除電作用によるも
ので、布地の帯電圧を一定値(コロナ放電開始電
圧)以下に保持する。これに対して制電剤を混合
した制電性繊維は、電荷の伝導拡散(接地)によ
る放電(減衰)効果を有する。両者を併用するこ
とにより、帯電圧をより低い一定値以下に抑え、
且つ早く減衰せしめることが出来る。
布地の帯電性は、静電気による塵埃、微生物の
吸着を防ぐ目的の他、半導体を取扱う工業におい
て半導体を静電気による破損や疲労を防止するた
めに必要である。このため布地を木製の台上に置
き、綿、羊毛又はアクリル繊維からなる摩擦布で
充分摩擦した後、台から引離した時の帯電圧(絶
対値)が6KV以下であることが好ましく、特に
3KV以下が好ましく、2KV以下が最も好ましい。
摩擦帯電の測定法は本発明者等が特開昭56−
48550号公報に開示した方法、特に同公報第2図
又は第3図に開示した装置によつて正確に測定す
ることが出来る。試料調整及び測定の雰囲気は25
℃、40%RHとする。(JIS L−1094(1980)B
法、所謂ロータリイスタチツクテスタによる摩擦
帯電圧の測定は誤差が大きく再現性に劣り好まし
くない)上記本発明者等が開示した方法で測定し
た帯電圧E(ボルト)と、フアラデーケージ法に
よつて測定した単位面積当りの布の電気量Q(ク
ーロン/m2)との間には、帯電圧8KV以下の領
域でQ=3×1010Eの関係が成立つことが確かめ
られている。すなわち帯電圧6KVは約1.8μC/
m2、3KVは0.9μC/m2、2KVは0.6μC/m2の電荷
密度に相当する。
編織物の発塵性の測定方法を第4図に示す。材
料21は上端を支持棒22に固定され、下端に荷
重23を取付けられ一定の張力が加えられる。一
方回転板24に複数個の摩擦補25が取付けられ
その表面は摩擦布26によつて覆われている。回
転板24が矢印方向に回転すると、試料21は摩
擦布26によつて間欠的に摩擦され、発生した塵
は空気吸引口27より吸引され粒子カウンター2
8により測定される。29は高性能をフイルター
で塵埃を除去された清浄空気の入口であり、30
はケースである。摩擦布8を省略すれば試料と摩
擦棒との摩擦による発塵を評価出来る。摩擦棒は
金属、セラミツクス、樹脂等を目的に応じて用い
ればよいが、一般に耐摩耗性の優れたものがよ
く、形も自由であるが、丸棒が一般的である。摩
擦布も任意であるが、耐摩耗性の優れたナイロ
ン、ポリエステルなどが好ましい。また26を試
料とし、21を摩擦布とすることも出来る。
以下の実施例では、試料は巾6cmとし、超音派
(溶融)切断により切断面の発塵を防止し、二つ
に折り(巾3cm)背面中央に切断部が来るように
取付け、荷重は60gとする。同じく摩擦棒は直径
8mm、長さ6cm、硬質アルミナ磁器で摩擦布は顔
料を含まぬナイロン6の40d/10fのトリコツト
(編物)を巾5cmに超音波切断したもので、切断
面が試料に接触しないように取付ける。円板11
の回転速度は30rpm(摩擦回数180回/分)とす
る。試料は清浄な水で洗浄しクリーンルーム中で
乾燥したものを用いる。測定装置まクリーンルー
ム(クリーンベンチではよい)内に設置する。粒
子カウンター15の空気吸引速度は0.5/分で
ある。
以下の実施例において部、%等は特記しない限
り重量比率とする。
実施例
分子量18000のPETを溶融し、紡糸口金内で静
止混合器で制電剤を連続混合し、285℃、直径
0.25mmのオリフイスから紡糸し、冷却、結油し
つゝ150m/分の速度で巻取り、80℃で3.3倍に延
伸し、150℃緊張熱処理して、150d/48fの制電糸
Y1を得た。制電剤は分子量7000のポリエチレン
オキシドとPETとの92/8共重合体で分子量35000
のものに、15%ドデシルベンゼンスルホン酸ナト
リウムを混合したものである。静止混合器は、特
開昭47−34166に開示されたもの(ケニツクス型)
12素子を直列に接続したもので、本発明者等が特
公昭47−49766に開示した混合器と同様の機能を
有している。なお制電剤を更に微細に分散するた
め紡糸オリフイスの手前に220メツシユのステン
レス鋼金鋼フイルターを設けた。制電剤は、繊維
横断面内で微細な多数の点状に分散し、長さ方向
には大部分が実質的に連続している。
Y1と同様にして得た75d/36fの制電糸をY2と
する。同じく通常のPET(非制電)延伸糸で
150d/48fのものをY3とし、75d/36fのものを
Y4とする。
更に、紡糸時にシリコン油(ポリメチルフエニ
ルシロキサン)を0.2%混合したPET(非制電)延
伸糸で150d/48fのものをY5とし、75d/36fのも
のをY6とする。なお沸水収縮率は制電糸が11%、
非制電糸は8%である。
Y4を経糸とし、但し織物1cm間隔に1本、ポ
リエステル導電繊維(鐘紡“ベルトロン”20d/
6f)を合糸したY4を配し、緯糸にY1を用いて得
た織物をF1とする。F1は、緯糸が経糸より太く、
張力が高く、且つ高収縮率であるために沈み、経
糸が浮いており、浮き高さは51μm、通気度は1.2
ml/cm3/秒、摩擦布羊毛での帯電圧(最高値)は
−1.8KVであつた。
F1とほヾ同様にして、但しY6を経糸に、Y1を
緯糸にして得織物をF2とする。F2の浮き高さは
55μmである。
比較のためY2を経糸に、Y1を緯糸に用いた織
物をF3とし、Y4を経糸に、Y3を緯糸に用いたも
のをF4とする。F3及びF4の浮き高さは夫々20μ
m、23μmであつた。
各織物の通気度、摩擦帯電圧、摩擦発塵性の測
定結果を第1表に示す。発塵性は摩擦開始後28分
後から32分後までの粒子数の平均で、粒径(μ
m)5以上、2以上、1以上、0.5以上、0.3以上
に区分して計数した。(有効数字3桁、四捨五入)
INDUSTRIAL APPLICATION FIELD The present invention relates to dustproof clothing. Precision industry, semiconductors,
So-called clean rooms are rapidly developing in the manufacturing process of pharmaceuticals, foods, etc., as well as in hospitals and fields that handle microorganisms, and there is a need for clothing with excellent dust resistance as working clothes in these clean rooms. This is related to dustproof clothing. Conventional technology The required performance of dustproof clothing is (a) high ability to prevent dust from passing through. (b) It is difficult for dust to adhere to it and it comes off easily; (c) it has low dust generation; (d) it has excellent antistatic properties; (e)
Comprehensive performance is required, including excellent chemical resistance. Polyethylene terephthalate is often used as a material for dustproof clothing, as shown in the examples of JP-A No. 55-30436, but it is unsatisfactory from the standpoint of antistatic properties. Problems to be Solved by the Invention From the standpoint of antistatic properties, it is preferable to use antistatic polyester fibers mixed with an antistatic agent. However, polyester generally has insufficient abrasion resistance and tends to break or fibrillate due to friction and generate dust, and this tendency is even more pronounced in antistatic polyester fibers mixed with an antistatic agent. In other words, antistatic properties and dustproof properties have contradictory properties. An object of the present invention is to provide an improved dustproof garment that has excellent antistatic properties and dust generation properties. Means for Solving the Problem The dust-proof clothing of the present invention has (a) a fabric made of polyester continuous filament plain weave, and (b) one of the warp and weft of the plain weave floats (float) and the other sinks. It has a (sinked thread) structure, and (iii) the sunken thread is an antistatic fiber mixed with an antistatic agent, and the floating thread is a non-antistatic fiber. Here, the polyester is not particularly limited, but for example, polyethylene terephthalate (hereinafter referred to as PET), polybutylene terephthalate (hereinafter referred to as PBT), etc.
) and a modified product in which a small amount (51% or less, particularly 10% or less) of a third component is copolymerized or mixed therewith is suitable. The weave structure must be plain weave. Cloth for dustproof clothing requires a structure with few voids from the viewpoint of preventing dust from passing through. The amount of voids can be evaluated by air permeability. Air permeability is JIS L-1096 (1979) A method (Fragile method)
Measured by Air permeability is usually 20 for twill fabrics.
ml/cm 3 /sec or more, but for dense plain weave it is 10
It is easy to set it to ml/cm 3 /sec or less. The air permeability is preferably 10 ml/cm 3 /sec or less, particularly preferably 5 ml/cm 3 /sec or less, and most preferably 2 ml/cm 3 /sec. However, if the air permeability is too low, the feeling of wearing will be poor, so it should be 0.1 ml/cm 3 /sec or more, especially 0.3 ml/cm 3 /sec.
Preferably, the time is seconds or more. Fabrics with low air permeability are made by weaving thin fibers (e.g., single threads of 3 d or less, especially 0.1 to 2 d) at high density, or shrinking with a high shrinkage rate (e.g., areal shrinkage rate of 10% or more, especially 20 to 50%). It is obtained by Furthermore, if necessary, the cloth can be pressed and densified by calendering or the like. Another feature of plain woven fabric is that it has a smooth surface and low dust adhesion, and has excellent abrasion resistance and triboelectric charging properties. As the antistatic agent to be mixed into the antistatic fiber, polyalkylene ethers such as polyethylene oxide, derivatives thereof, and copolymers (e.g., ether/ester block copolymers) are suitable, and they are further added with hydroxyl groups, amino groups, and carboxyl groups. Introducing polar groups such as groups, sulfone groups, and their metal salts,
It is also preferable to mix (combine) an organic compound having a polar group. As the mixed structure, a fluid mixture in which the antistatic agent is dispersed in the form of fine particles (acicular particles in many cases) in polyester (matrix) is also used; As disclosed in the above publication, antistatic agents are those in which the antistatic agent is dispersed in many fine dots (nebula-like) in the cross section of the fiber and has a substantially continuous linear structure in the length direction. It is most preferred because it has excellent antistatic properties and therefore sufficient antistatic properties can be obtained with a small mixing ratio. For example, in the case of polyethylene oxide-based nonionic polymers, it is 1 to 5%.
If 10 to 20% of an ionic compound such as sodium alkylbenzenesulfonate is mixed with the
Approximately 0.1 to 2%, i.e. 1/2 to 1/2 compared to granular mixture
Excellent antistatic properties can be obtained at a mixing ratio of about 1/10. However, polyester fibers mixed with an antistatic agent have a slightly stronger tendency to fibrillate due to friction and the like and cause dust generation than those without the antistatic agent. This tendency is stronger as the mixing ratio of the antistatic agent increases (continuous linear mixing is therefore preferred). In any case, since antistatic fibers often have somewhat poor resistance to abrasion, they are used as sinking yarns, and non-antistatic yarns with excellent abrasion resistance are used as floating yarns. FIG. 1 is a perspective explanatory view of a plain weave used in the present invention. In the figure, 1 is a floating line and 2 is a sinking line.
FIG. 2 is a cross-sectional view of the fabric shown in FIG. 1 in one direction of the floating yarn, and FIG. 3 is a cross-sectional view of the fabric in the second direction of the sinking yarn. In Fig. 2, dotted lines 10 to 10' are the surface of the float;
The dotted line 20-20' is the surface of the precipitated yarn. Surface 10-
The distance A between 10' and surface 20-20' is the "floating height"
It is written as In general, plain weave does not have a structure in which one of the warp and weft sinks and the other floats, and A is often close to zero. However, by changing the tension during weaving and the thickness (hardness) of the warp and weft, the floating height A can be increased to 10 μm or more, especially 20 μm or more.
The thickness can be set to 100 μm, and the probability that the precipitated thread will come into contact with an external object and be damaged can be greatly reduced. That is, by increasing the tension of one of the warp or weft during weaving, it is possible to make it a sink yarn. Similarly, one thread can be made to sink by shrinking it more than the other, or by making it thicker (harder). Furthermore, the floating height can be further increased by combining two or more of the above three methods (high tension, high shrinkage, thick yarn). The float is a non-static polyester fiber. It is desirable that the floating yarn has excellent abrasion resistance. for example,
In addition to homopolymers such as PET and PBT, it is preferable to copolymerize or mix them with a third component to reduce the coefficient of friction or improve wear resistance. Components that reduce the coefficient of friction (for example, the coefficient of friction against metals) include paraffin, polyolefin, polyalkylene ether, compounds with alkyl groups, organic silicon compounds (for example, polyorganosiloxane, etc.), and organic fluorine compounds (for example, polyfluorinated ethylene). derivatives, etc.), or a combination of two or more thereof. Mixing ratio is 0.001~
About 10%, particularly 0.1 to 5%, is often suitable. The fabric must be antistatic. Woven fabrics using antistatic polyester fibers as wefts have fairly excellent antistatic properties, but if even higher antistatic properties are required, conductive fibers can be used in combination. Conductive fibers include metal fibers, metal-plated fibers, metal compounds (semiconductors, etc.), and other conductive substances (specific resistance).
10 7 Ω・cm or less) on the surface or inside, fibers that have on the surface or inside a conductive layer made of resin mixed with conductive particles or highly conductive components, etc. Examples of the conductive particles include carbon black, metal particles, metal compound particles, and particles having a thin layer of metal or metal compound on their surfaces. Among them, the most suitable is a composite fiber in which a conductive layer containing conductive particles and a protective layer made of a fiber-forming polymer are bonded together. The electrical resistance per 1 cm length of the conductive fiber is preferably 10 11 Ω or less, most preferably 10 8 Ω or less. The conductive fibers can be combined or twisted with antistatic fibers or non-static fibers, and interlaced with the weft and/or warp, for example, at regular intervals. The antistatic effect of conductive fibers is due to the neutralizing effect of corona discharge, which keeps the charged voltage of the fabric below a certain value (corona discharge starting voltage). On the other hand, antistatic fibers mixed with an antistatic agent have a discharge (attenuation) effect due to conduction and diffusion (grounding) of charges. By using both together, the electrostatic voltage can be kept below a lower fixed value,
Moreover, it can be attenuated quickly. The electrostatic property of fabric is necessary not only to prevent the adsorption of dust and microorganisms due to static electricity, but also to prevent semiconductors from being damaged or fatigued by static electricity in industries that handle semiconductors. For this reason, it is preferable that the electrostatic voltage (absolute value) when the fabric is placed on a wooden table, rubbed sufficiently with a friction cloth made of cotton, wool, or acrylic fiber, and then removed from the table, is 6 KV or less, especially
3KV or less is preferred, and 2KV or less is most preferred.
The method for measuring frictional electrification was developed by the present inventors in Japanese Unexamined Patent Application Publication No. 1986-
Accurate measurement can be achieved by the method disclosed in Japanese Patent No. 48550, particularly by the apparatus disclosed in FIG. 2 or 3 of the same publication. The atmosphere for sample preparation and measurement is 25
℃, 40%RH. (JIS L-1094 (1980) B
(Measuring the frictional charge voltage using a so-called rotary static tester is not preferable because it has large errors and poor reproducibility.) It has been confirmed that the relationship Q=3×10 10 E holds between the amount of electricity Q (coulombs/m 2 ) of the cloth per unit area and the charged voltage is 8 KV or less. In other words, the charged voltage of 6KV is approximately 1.8μC/
m2 , 3KV corresponds to a charge density of 0.9μC/ m2 , and 2KV corresponds to a charge density of 0.6μC/ m2 . Fig. 4 shows a method for measuring dust generation of knitted fabrics. The upper end of the material 21 is fixed to a support rod 22, and a load 23 is attached to the lower end to apply a constant tension. On the other hand, a plurality of friction auxiliaries 25 are attached to the rotary plate 24, and their surfaces are covered with a friction cloth 26. When the rotating plate 24 rotates in the direction of the arrow, the sample 21 is intermittently rubbed by the friction cloth 26, and the generated dust is sucked through the air suction port 27 and transferred to the particle counter 2.
8. 29 is the inlet of clean air from which dust is removed by a high-performance filter;
is the case. If the friction cloth 8 is omitted, dust generation due to friction between the sample and the friction rod can be evaluated. The friction rod may be made of metal, ceramics, resin, etc. depending on the purpose, but it is generally good to have excellent wear resistance, and the shape can be arbitrary, but round rods are common. The friction cloth is also optional, but nylon, polyester, etc., which have excellent abrasion resistance, are preferable. Further, it is also possible to use 26 as a sample and 21 as a friction cloth. In the following example, the sample is 6 cm wide, ultrasonic (melting) cutting is used to prevent dust from being generated on the cut surface, and the sample is folded in half (3 cm wide) and mounted so that the cut part is at the center of the back. The weight shall be 60g. Similarly, the friction rod is made of hard alumina porcelain with a diameter of 8 mm and a length of 6 cm, and the friction cloth is a 40D/10F tricot (knitted fabric) of nylon 6 that does not contain pigments and is ultrasonically cut into a width of 5 cm, with the cut surface in contact with the sample. Install it so that it does not. Disk 11
The rotation speed of is 30 rpm (number of frictions: 180 times/min). Use samples that have been washed with clean water and dried in a clean room. Install the measuring device in a clean room (a clean bench is fine). The air suction rate of the particle counter 15 is 0.5/min. In the following examples, parts, percentages, etc. are expressed as weight ratios unless otherwise specified. Example: PET with a molecular weight of 18,000 was melted, an antistatic agent was continuously mixed in a spinneret with a static mixer, and the temperature was 285℃ and the diameter
Spun from a 0.25mm orifice, cooled, oil-bound, wound at a speed of 150m/min, stretched 3.3 times at 80℃, and subjected to tension heat treatment at 150℃ to produce 150d/48f antistatic yarn.
Got Y1. The antistatic agent is a 92/8 copolymer of polyethylene oxide with a molecular weight of 7,000 and PET and has a molecular weight of 35,000.
and 15% sodium dodecylbenzenesulfonate. The static mixer is the one disclosed in JP-A-47-34166 (Kenix type)
It has 12 elements connected in series, and has the same function as the mixer disclosed by the present inventors in Japanese Patent Publication No. 47-49766. In order to further finely disperse the antistatic agent, a 220-mesh stainless steel filter was installed in front of the spinning orifice. The antistatic agent is dispersed in the form of a large number of fine dots within the cross section of the fiber, and most of the antistatic agent is substantially continuous in the length direction. Let Y2 be the 75d/36f antistatic yarn obtained in the same manner as Y1. Similarly, with normal PET (non-antistatic) drawn yarn
The 150d/48f one is Y3, and the 75d/36f one is Y3.
Let's say Y4. Furthermore, PET (non-antistatic) drawn yarn mixed with 0.2% silicone oil (polymethylphenylsiloxane) during spinning, 150d/48f, is designated as Y5, and 75d/36f is designated as Y6. The shrinkage rate in boiling water is 11% for antistatic yarn.
The non-antistatic yarn is 8%. Y4 is used as the warp thread, however, polyester conductive fiber (Kanebo "Beltron" 20d/
F1 is a fabric obtained by arranging Y4 which is a double yarn of 6f) and using Y1 for the weft. In F1, the weft is thicker than the warp.
Due to its high tension and high shrinkage rate, it sinks and the warp threads float, with a floating height of 51 μm and air permeability of 1.2.
ml/cm 3 /sec, and the charging voltage (maximum value) on the friction fabric wool was -1.8 KV. Make the fabric F2 in the same manner as F1, but use Y6 as the warp and Y1 as the weft. The floating height of F2 is
It is 55 μm. For comparison, a fabric using Y2 for the warp and Y1 for the weft is called F3, and a fabric using Y4 for the warp and Y3 for the weft is called F4. The floating height of F3 and F4 is 20μ each.
m, 23 μm. Table 1 shows the measurement results of air permeability, frictional charging voltage, and frictional dust generation of each fabric. Dust generation is the average number of particles from 28 minutes to 32 minutes after the start of friction, and the particle size (μ
m) Counted by dividing into 5 or more, 2 or more, 1 or more, 0.5 or more, and 0.3 or more. (3 significant figures, rounded off)
【表】【table】
【表】
発明の効果
第1表から明らかのように、本発明品は制電性
及び防塵性が共に優れている。これは沈糸に制電
糸を用い、浮糸に非制電糸を用いたために得られ
るものである。[Table] Effects of the Invention As is clear from Table 1, the product of the present invention has excellent antistatic properties and dustproof properties. This is obtained because an antistatic yarn is used for the sinking yarn and a non-static yarn is used for the floating yarn.
第1図は本発明防塵衣の衣地の斜視説明図、第
2図は浮糸方向の断面図、第3図は沈糸方向の断
面図である。第4図は発塵性の測定方法の説明図
である。
FIG. 1 is a perspective explanatory view of the dustproof clothing of the present invention, FIG. 2 is a cross-sectional view in the floating direction, and FIG. 3 is a cross-sectional view in the sinking direction. FIG. 4 is an explanatory diagram of a method for measuring dust generation.
Claims (1)
織物からなり、 (ロ) 該平織物は経糸及び緯糸の一方が浮き(浮
糸)他方が沈む(沈糸)構造を有し、且つ (ハ) 沈糸は制電剤を混合された制電繊維であり、
浮糸は比制電繊維である。 ことを特徴とする防塵衣。 2 浮糸の表面と沈糸の表面の平均間隔(浮き高
さ)が20〜100μmである特許請求の範囲第1項
記載の防塵衣。 3 非制電繊維の表面積の50%以上を占める成分
が、パラフイン、ポリオレフイン、ポリアルキレ
ンエーテル、アルキル基を有する化合物、有機シ
リコン化合物及び有機弗素化合物の群から選ばれ
た少なくとも1種の滑剤を含有し摩擦係数を低減
せしめられたポリエステルよりなる。特許請求の
範囲第1項記載の防塵衣。[Scope of Claims] 1 (a) The fabric is made of polyester continuous filament plain woven fabric, (b) The plain woven fabric has a structure in which one of the warp and weft yarns is floating (floating yarn) and the other is sinking (sinking yarn), and (c) the precipitated yarn is an antistatic fiber mixed with an antistatic agent,
The float is a specific antistatic fiber. Dust-proof clothing characterized by: 2. The dust-proof clothing according to claim 1, wherein the average distance (floating height) between the surface of the floating thread and the surface of the sinking thread is 20 to 100 μm. 3 A component occupying 50% or more of the surface area of the non-antistatic fiber contains at least one lubricant selected from the group of paraffin, polyolefin, polyalkylene ether, compound having an alkyl group, organic silicon compound, and organic fluorine compound. Made of polyester that has a reduced coefficient of friction. Dust-proof clothing according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59191242A JPS6170004A (en) | 1984-09-11 | 1984-09-11 | Dust-proof garment |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59191242A JPS6170004A (en) | 1984-09-11 | 1984-09-11 | Dust-proof garment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6170004A JPS6170004A (en) | 1986-04-10 |
| JPH0351802B2 true JPH0351802B2 (en) | 1991-08-08 |
Family
ID=16271261
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59191242A Granted JPS6170004A (en) | 1984-09-11 | 1984-09-11 | Dust-proof garment |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6170004A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01221547A (en) * | 1988-03-01 | 1989-09-05 | Teijin Ltd | Woven fabric for dust-free garment |
-
1984
- 1984-09-11 JP JP59191242A patent/JPS6170004A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6170004A (en) | 1986-04-10 |
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