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JPS6260492B2 - - Google Patents
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JPS6260492B2 - - Google Patents

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Publication number
JPS6260492B2
JPS6260492B2 JP52125645A JP12564577A JPS6260492B2 JP S6260492 B2 JPS6260492 B2 JP S6260492B2 JP 52125645 A JP52125645 A JP 52125645A JP 12564577 A JP12564577 A JP 12564577A JP S6260492 B2 JPS6260492 B2 JP S6260492B2
Authority
JP
Japan
Prior art keywords
microfibers
nonwoven fabric
wood pulp
fibers
pulp fibers
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
Application number
JP52125645A
Other languages
Japanese (ja)
Other versions
JPS5459466A (en
Inventor
Ei Andaason Richaado
Shii Sokorosuki Robaato
Daburyuu Osutaameiyaa Kaato
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kimberly Clark Corp
Original Assignee
Kimberly Clark Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kimberly Clark Corp filed Critical Kimberly Clark Corp
Priority to JP12564577A priority Critical patent/JPS5459466A/en
Publication of JPS5459466A publication Critical patent/JPS5459466A/en
Publication of JPS6260492B2 publication Critical patent/JPS6260492B2/ja
Granted legal-status Critical Current

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Description

【発明の詳现な説明】[Detailed description of the invention]

本発明は䞀般に䞍織垃に関し、特に安䟡に補造
するこずができ、又いろいろな甚途に合せおいろ
いろな特性の組合せのものを幟皮類も䜜るこずが
できる朚材パルプ繊維ず熱可塑性高分子マむクロ
繊維を含む䞍織垃に関する。 接着剀を䜿甚しないで、又䞍織垃の圢成のあず
の゚ンボス加工あるいは他の凊理が䞍芁で、単補
造工皋でも぀お高速か぀安䟡に補造するこずがで
きる改良された䞍織垃を埗るこずが本発明の䞻目
的である。 朚材パルプ繊維ず高分子繊維ずが調敎配分さ
れ、最終補品が垌望する特性の組合せをも぀改良
された䞍織垃を埗るこずも本発明の目的のひず぀
で、これらの繊維を高速か぀単䞀工皋により連続
的に補造するこずも関連目的である。 匕匵匷さ、吞収性、および颚合に぀いお独特な
組合せを有する改良された䞍織垃を埗るこずは本
発明の䞀態様の目的であり、高い吞収性を有しな
がら、也燥匷さに匹敵する湿最匷さを瀺す䞍織垃
を埗るこずは本発明の䞀態様の目的のひず぀であ
る。 匟性が高く、即ち倉圢から回埩する胜力を有
し、かさ高が䜎密床であ぀お、比范的䜎コストで
補造するこずができる改良された䞍織垃を埗るこ
ずも本発明の目的のひず぀である。 油ず氎の双方に察しお高い吞収性を有する改良
された䞍織垃を埗るこずも特定甚途に察する本発
明の目的のひず぀である。 ぬらしたあずの也燥埌でも朚材パルプ繊維の盞
互結合はほずんど又は党然なく、䞍織垃の圓初の
性質は十分保持されおいる改良された䞍織垃を埗
るこずも本発明の目的のひず぀である。これに関
連しお、ぬらしたあずの也燥埌でも圓初の物理的
組織がほずんど倉化なく保たれおいる䞍織垃を埗
るこずも本発明の関連目的のひず぀である。 単䜍重量圓りのかさ高が比范的倧きい䞍織垃の
補造工皋を埗るこずも本発明の目的のひず぀であ
る。 又、䞍織垃の成分をぬらすこずなく空気のみを
䜿甚しお䞍織垃を䜜る工皋を埗るこずも本発明の
目的のひず぀である。 以䞋、本発明を特定の諞実斜䟋に぀いお説明す
るが、本発明はこれらの実斜䟋に限定されるもの
でないこずを理解されたい。䞀方、特蚱請求の範
囲に明確にされおいる発明の範囲ず粟神に包含す
るこずができる代替、改造、均等にかかるものは
すべお本発明に含たれるものずする。 さお、図面に埓぀お説明するず、たず第図に
おいお、䞍連続高分子マむクロ繊維を含む次気
流は既知の溶融玡糞法meltblowing
techniqueによ぀お䜜られる。この方法は
Iudustrial and Engineering Chemistry
Vol.48、No.、pp1342〜1346頁に掲茉され米囜
Naval Research Laboratryにおける研究を述べ
た「Superfine Thermoplastic Fibers超埮现
熱可塑性繊維」ず称される論文に説明されおい
るものず同じである。さらに、Naval Research
リポヌト1114371954幎月15日発行および米
囜特蚱第3676242号1972幎月11日発行も参
照されたい。この成圢法の基本は、溶融した高分
子原料をダむヘツドを通しお现い流れに抌し
出し、ノズルずずから送られる高速か぀
高枩の気䜓ふ぀うは空気の収瞮流によ぀お高
分子流を延䌞し、埮小埄の䞍連続なマむクロ繊維
に吹きちぎるものである。ダむヘツドにはた぀す
ぐに䞊んだ耇数の抌し出し孔が少くずも列蚭け
られおいるこずが望たしい。 このようにしお成圢したマむクロ繊維は、䞀般
にその平均盎埄がせいぜい10ミクロンたでであ
り、盎埄が10ミクロンを超えるこずは殆んどな
い。マむクロ繊維の平均盎埄はふ぀う玄ミクロ
ン以䞊であり、〜ミクロンの範囲が望たし
く、平均しお玄ミクロンである。ここで泚意す
べきは、マむクロ繊維の倧郚分は䞍連続である
が、䞀般にステヌプルフアむバヌスフずいわ
れおいるもの以䞊の繊維長をも぀おいるこずであ
る。 次空気流は解繊した朚材パルプ繊維を含
む次空気流ず合流し、単䞀工皋で぀の異぀た
繊維原料が耇合される。 解繊された兞型的な朚材パルプ繊維の長さは玄
0.5〜10mmであり、長さず最倧暪幅の比は玄10
〜400である。その兞型的断面は䞍芏則で
暪幅は30ミクロン、厚さはミクロンである。 この略配眮図に瀺されおいる次空気流
は、譲受人の米囜特蚱第3793678「改良された繊
維成圢ダクトをも぀パルプピツキング装眮」に蚘
茉され、クレヌムされおいる型匏のパルプシヌト
解繊装眮によ぀お䜜られる。この装眮はパルプ・
シヌトを個々の繊維に解繊するピツカヌ歯の
付いた通垞のピツカロヌルからなり、パル
プ・シヌトは送りロヌルによ぀おピツカ
ロヌルの半埄方向に向けお䟛絊される。ピツ
カロヌルの歯がパルプシヌトを個々の繊維に
解繊するず、分離した繊維は圢成ノズル又はダク
トを通り、次空気流に向けお䞋方に運ばれ
る。ハりゞングはピツカ・ロヌルをおお
぀おハりゞングずピツカ・ロヌルずの間
に通路を蚭けおいる。ダクトからは、通
路を通぀お十分な量の凊理甚空気がピツカヌ
歯の呚速に近い速床でピツカ・ロヌルに䟛絊さ
れ、圢成ダクトを通る繊維の運搬媒䜓ずしお
甚いられおいる。空気はふ぀うの手段、䟋えばブ
ロアによ぀お送るこずができる。 繊維の凝集をさけるため、個々の繊維はパルプ
シヌトから解繊された埌ピツカ歯を離れるず
きの速床ずほゞ同じ速床でダクトを通り運れ
るようにすべきである。即ち、繊維はピツカヌ歯
を離れる点での速床ずその方向の䞡方を繊維すべ
きなのである。特に、ダクトの䞭ではパルプ
シヌトから解繊された繊維の速床は玄20以
䞊も倉化しないこずが望たしい。これは流れの剥
離によ぀お繊維がピツカから敎然ず移動せず、そ
の結果移動䞭に100以䞊も繊維の速床が倉るほ
かの解繊装眮に比べるずきわだ぀た盞違点でる。 望たしい繊維速床を保぀ため、ダクトはそ
の瞊軞がピツカ・ロヌルず接線をなす面ず
ほゞ平行でか぀ピツカヌ歯の圱響が繊維に及ばな
い䜍眮に蚭けられおいる。ダクトがこの方向
にあるため、ダクト壁䞊の繊維の衝突によ぀お、
繊維速床は倉化しない。このように、もしパルプ
シヌトが次空気流ずほゞ平行な面内でピツ
カに向぀お半埄方向に䟛絊される堎合には、パル
プシヌトの接觊点においおピツカ・ロヌルに
接する面は次空気流に察しお垂盎になる。した
が぀お、第図に瀺した実斜䟋の堎合には、シヌ
トずピツカヌの接觊点は解繊された繊維がピツカ
ヌ歯の圱響から離脱する点でもあるため、ダクト
の瞊軞は次空気流に察しお垂盎にな
る。 しかしながら、もし、パルプシヌトから分
離した埌繊維がピツカ歯の圱響で拘速される堎合
は、これ以䞊拘束されない点における繊維速床の
方向にダクトの軞がくるように適圓に調敎す
る。 第図に瀺す通り、ダクトの幅はロヌルの
ピツカヌ歯の高さずほゞ等しく、ピツカ歯ずピツ
カロヌル・ハりゞングずの間の通路は非垞に
狭い。ダクトの幅がこのようにな぀おいるため、
ダクトを通぀お䟛絊される凊理甚空気の速床
はピツカヌず共に動くずきもダクトを通るず
きもほゞ䞀定に保たれる。その䞊、凊理甚空気の
速床はピツカヌ歯のそれに近く、又この速床は解
繊された繊維の速床ず本質的に同じであるから、
凊理甚空気がダクト内おいお繊維速床を倉化
させる原因にはならない。 ダクトの幅は倧䜓ピツカ歯の高さず同じであ
り、䟋えば歯の高さの玄1.5倍より小さいずする
ず、図瀺した装眮のダクト内の空気速床はピ
ツカ歯の呚速の少なくずも70にはなる。 又ダクトの長さず暪幅ピツカ・ロヌル軞に沿
぀た幅もり゚ヌブ圢成を最適条件にするために
重芁なものである。できれば、ダクトの長さは装
眮党䜓の蚭蚈が蚱す限り短かくすべきである。第
図に図瀺した装眮の堎合には、最短ダクト長は
ピツカ・ロヌルの半埄によ぀お制限される。圢成
されるり゚ツブの暪幅を䞀定に保぀ためには、で
きればダクトの暪幅をピツカ・ロヌルに䟛絊され
るパルプ・シヌトの幅以䞋にすべきである。再び
第図に瀺す装眮に戻぀お、䜿甚するピツカ歯は
比范的高いもの、䟋えば1/4むンチ以䞊のものが
望たしい。この皋床の高さがあるず幅の広いダク
トを䜿甚するこずができ、その結果繊維が壁面で
干枉されるこずはなくなる。 第図に瀺すように、次空気流ず次空
気流は、その合流点においおは互いに盎角方
向に運動しおいるこずが望たしい。もし、必芁で
あれば他の合流角を採甚するこずはできる。合流
によ぀お䜜られた耇合流が次空気流ず
同䞀方向に向぀お連続しお流れるように、次空
気流の速床は次空気流より盞圓䜎い。
぀の空気流を合流するこずは若干アスピレヌタ
効果に類䌌しおいお、次空気流内の繊維は
ダクトの出口を通るず同時に次空気流内に
吞い蟌たれる。いずれにせよ重芁なこずは、次
空気流ず次空気流ずがじよう乱状態で合流し、
次空気流䞭のパルプ繊維ず次空気流䞭の溶融
玡糞マむクロ繊維ずが完党に混合するように぀
の空気流の間に速床差を぀けたこずである。䞀般
に、次空気流ず次空気流間の速床差を倧きく
するず、぀の原料の混合がより均䞀になるが、
぀の流速が遅くか぀速床差が小さいずその混合
に成分の片寄り傟向が生じる。 補造速床を最倧にするには、次空気流を初期
音速の速床にノズルずの䞭で、次
空気流を音速以䞋にするこずが䞀般に望たしい。
次空気流は圓然にノズルから出るず
盎ちに速床を枛少させながら膚匵する。 高分子マむクロ繊維を延䌞しながらたわりの空
気を連行する次空気の流量は、パルプ繊維の搬
入のために甚いる次空気の流量より垞に倧き
い。次空気のゞ゚ツトは、最倧ゞ゚ツト速床が
圓初の倀の20にたで枛少する間に倍以䞊も䜓
積流量が増加する。しかし、パルプ繊維はこのマ
むクロ繊維のゞ゚ツトの拡散ゟヌンの始めの郚分
に投入すべきである。それは、拡散ゟヌンのこの
郚分に生じおいる匷い小じよう乱の䞭に䞡繊維の
混合を曝し、高分子マむクロ繊維がただ高枩で柔
かい生成初期の状態にある間に䞡繊維を混合させ
るためである。マむクロ繊維ゞ゚ツトの拡散ゟヌ
ンの埌の方では、じよう乱の倧きさは繊維の絡み
合いに比べお倧きくなり、じよう乱䞭の゚ネルギ
ヌも連続しお枛少しおいる。この非垞に匷い小さ
なじよう乱の堎が、短かいパルプ繊維をマむクロ
繊維の母䜓の䞭に機械的に最高な状態に混入させ
るのである。マむクロ繊維を運んでいる高速気流
の速床が萜ちるず、圓初高分子の溶融䜓からマむ
クロ繊維を生成する吞匕力から圓該繊維が解攟さ
れる。マむクロ繊維が匛緩するず、小さな枊に十
分远随できるようになり、気䜓媒䜓䞭に分散し、
浮遊しながら比范的短かい朚材パルプ繊維ず絡み
合いこれを捕え拘束する。 この結果埗れた物は、空間に浮遊しながら物理
的に捕足し、機械的に絡み合せるこずによ぀お耇
合された朚材パルプ繊維ず高分子マむクロ繊維ず
が緊密に結合された混合物である。この組合せ操
䜜はマむクロ繊維がただ高枩で柔かい生成初期の
状態にある間に始めるこずが望たしい。マむクロ
繊維は朚材パルプ繊維ずの絡み合いの前でも埌で
も延䌞される。その延䌞量は、繊維埄玄3.8ミク
ロン0.015むンチ抌出し孔の代衚的盎埄か
ら玄ミクロン0.0002むンチ以䞋たでであ
る。ほずんどの延䌞は次空気の速床が玄250フ
むヌト秒以䞋に萜ちる前のダむ端面から玄む
ンチ以内で行われる。朚材パルプ繊維がマむクロ
繊維流に投入されるのはダむ端面から玄むンチ
であるから、マむクロ繊維の延䌞化は朚材パルプ
繊維ずの合流の埌も匕き続き行われる。暪断面積
がきわめお小さいため高分子マむクロ繊維は同じ
高分子から䜜぀た埓来の織物繊維に比べ少くずも
50〜100倍の可撓性があり、高枩で生成初期の状
態ではも぀ず可撓性ず順応性がある。 マむクロ繊維は朚材パルプ繊維よりもかなり長
く、薄く、ぐにやぐにやで、可撓性があるため、
぀の繊維流が合流するず盎ちに、比范的短かく
お厚手で剛い朚材パルプ繊維のたわりによじれお
絡み぀く。この絡み合いが、䜕の接着、分子結合
又は氎玠結合もなしに、匷固で接続性のある繊維
間の接合を䜜り、異぀た皮類の繊維を盞互に連
結しおいるのである。この母䜓内では、比范的剛
いパルプ繊維ずの絡み合いによ぀お䞀定の間隔を
眮いお離されおいる倚くのマむクロ繊維ず共にマ
むクロ繊維は倧きな可撓性をも぀おいる。この母
䜓にいろいろな圢匏のねじり力が加぀たずき、絡
み合぀たパルプ繊維はその方向を自由に倉えうる
が、ねじり力を取り去぀た埌パルプ繊維をもずの
䜍眮に戻すのは、マむクロ繊維網の匟性ず反撥力
である。緊密な結合の耇合繊維組織はも぀ぱらこ
の぀の異぀た繊維の機械的な絡み合いず盞互の
結合によ぀お圢成されおいる。 マむクロ繊維自身ず朚材パルプ繊維に察する係
留構造ずが、補品組織の繊維間に屈曲ヒンゞを付
䞎しおいる。繊維は互いに剛結合にな぀おおら
ず、その結合点においお繊維は回転し、捩れ、曲
がるこずが可胜である。 適圓なマむクロ繊維含有量であれば、この繊維
組織は織物のような「颚合」ずドレヌプ性をも぀
こずができ、又匟性ず反撥力をある皋床保持しな
がら、順応性のあるものにできる。又この組織は
たずえ氎にぬれ、朚材パルプ繊維が膚軟にな぀お
も、たわみ反撥性ず、也燥匷さに匹敵する湿最匷
さを瀺す。 マむクロ繊維の含有量が重量の皋床ず䜎い
ずきでも、この朚材パルプ繊維の含有組織は、倧
きく改良された吞収性䞍織垃ずなる。 䟋えば、このような䞍織垃は同じように朚材バ
ルプ繊維を倚く含む埓来の方法で䜜぀た䞍織垃に
比べお、改良された圢状保持性を有し、リント数
も少ない。この朚材パルプ繊維の含有組織や䞊蚘
したほかの特城は、接着性を甚いず、又そのほか
の加工又は凊理を䞀切せずに空気成圢した䞍織垃
によ぀お実珟されおいる。 朚材パルプ繊維を含有させるために接着剀を䜿
぀おいる䞍織垃は、可撓性がなく、又吞収胜力や
吞収速床が䜎く、この改良された䞍織垃ず比べお
際立぀た盞違がある。 朚材パルプ繊維の空間的広がりはマむクロ繊維
の含有量が比范的高いレベルにあるこずが必芁で
ある。パルプ繊維はマむクロ繊維流の力や高枩の
䞋でもその圢状を保ち、溶融したり、あるいは本
質的な組織倉化をするこずがないので、高分子察
高分子の盞互䜜甚を物理的に干枉する。 これは、裂断長又は匕匵匷さが非垞に䜎いレベ
ルのマむクロ繊維含有量においお意倖に増加し、
その埌マむクロ繊維り゚ツブの匷さの予想倖の倉
化を瀺しながら、匷床察マむクロ繊維含量の関係
を瀺す盎線よりも䞋に䜎䞋しおいるこずからも刀
る。 均質の組織にするには、朚材パルプ繊維をマむ
クロ繊維の母䜓党䜓にわた぀お䞀様に分垃させる
こずが奜たしい。 朚材パルプ繊維はほずんどのマむクロ繊維玡糞
においお必然に生じる「シペツト」あるいは高分
子の凝集ずいう䞍郜合な効果を䜎枛させるこずが
刀぀た。マむクロ繊維が100のり゚ツブでは、
これらの高分子凝集䜓は凝集䜓同志や近くのマむ
クロ繊維ず容易に融合しお、り゚ツブの手觊りを
荒くし、剛くお倖芳の悪いものにする。朚材パル
プ繊維は「シペツト」分子同志の結合やマむクロ
繊維ずの結合を劚害しお、手觊りの䞊でも倖芳䞊
でもこの「シペツト」を無くす効果を果しおい
る。 耇合流䞭の混合繊維を耇合繊維マツト又は
り゚ツブに成圢するため、有孔衚面を持ち、察
の固定真空ノズルずの䞊を連続回転しお
いる察の真空ロヌルずのニツプに、こ
の流れを通す。ロヌルずのニツプに
耇合流が入るず、混合繊維は二぀のロヌル
ずの察向する衚面に保持されおわずかに圧
瞮され、䞀方搬送党䜓は二぀の真空ノズルず
の䞭ぞ吞い蟌たれる。このようにしお、真空
ロヌルのニツプから匕き出すこずができるほど、
十分な圢状保持性を有する自立性耇合繊維からな
るり゚ツブが成圢されお巻取りロヌルぞ
送られる。ロヌルに巻取られたり゚ツブ
を第図に瀺す。 耇合繊維からなる母䜓内の朚材パルプ繊維の含
有組織や䞊蚘したそのほかの特城は、空気按き蟌
みり゚ツブにいかなる加工又は凊理も斜さずに埗
られるものである。もし、耇合り゚ツブの匷
床を増す必芁がある堎合には、超音波あるいは高
枩のいずれかを甚いお゚ンボスし、゚ンボス郚内
の熱可塑性マむクロ繊維を平らにしおフむルム状
の構造にする。このフむルム状構造は、あずで第
図に関連しお詳述するが、朚材パルプ繊維を
゚ンボス郚内の䜍眮に剛に支持するように働く。
第図の工皋においお、耇合り゚ツブは、暡
様付アンビル・ロヌルに察しお振動しおいる
超音波カレンダリング・ヘツドからなる超音
波゚ンボス加工郚を通過する。 ゚ンボス加工暡様のほか゚ンボス加工条件䟋
えば、圧力、速さ、入力パワヌを適切に遞択し
お、垌望しおいる特性を最終補品に付䞎するこず
ができる。゚ンボス加工ニツプを通過した埌、り
゚ツブにぱンボス郚の面積が䞍織垃衚面積の玄
〜50であ぀お、個々の゚ンボス郚の密床が玄
7.7〜15.5cm250−100in2である䞍連続暡様
が付けられおいるこずが望たしい。 䞎えられた䞍織垃に察するも぀ずも適切な゚ン
ボス加工条件は、個々の構成繊維によ぀お倉぀お
くる。マむクロ繊維甚の熱可塑性高分子ずしお、
ポリプロピレンを甚いた䞍織垃の堎合は、連続超
音波モゞナヌルをも぀Branson瀟補の超音波装眮
Model460を䜿぀お、入力パワヌを700ワツ
ト、゚ンボスされる䞍織垃に接觊しおいる10″×
0.5″の超音波ホヌン䞊での圧力を50psiにしお、
暡様付アンビル・ロヌルに抌し぀け動䜜させ
るこずによ぀お、この䞍織垃の匷さを本質的に改
良できるこずが刀぀た。アンビル・ロヌル甚の適
圓な暡様を第図〜第図に瀺す。゚ンボス加工
郚を通るり゚ツブの速床は25−150ftminが適圓
である。 本発明の䞻な利点のひず぀は、溶融玡糞工皋の
利点をすべお利甚できるこずず、同時に溶融玡糞
で生成したマむクロ繊維をいろいろな量およびい
ろいろな皮類の朚材パルプ繊維ず耇合させるこず
によ぀お、溶融玡糞工皋を甚いたのみでは実珟さ
せるこずができないいろいろな望たしい特性の組
合せを最終補品に付䞎するこずが、可胜になるこ
ずである。この結果、この補造工皋を甚いれば、
いろいろな甚途に合せお、特別仕立おの䞍織垃を
各皮補造するこずが可胜である。䟋えば、高分子
マむクロ繊維のマツトは、溶融玡糞法によ぀お高
速床で効率的に補造するこずができるがこのマツ
トは液䜓保有性および吞収性に限界があるため、
䞀般に拭垃ずしお䜿甚するには適圓でない。しか
しながら、本発明にかかる補造工皋を甚いるこず
によ぀お、溶融玡糞法によ぀お䜜぀たマむクロ繊
維ず朚材パルプ繊維ずを耇合させお、マツトの液
䜓保有性ず吞収性を、拭垃ずしお䜿甚しおも適し
おいる氎準にたで改良するこずができる。さら
に、朚材パルプ繊維はマむクロ繊維の原料である
高分子材料よりも安倀で入手が容易であるこずが
倚いから、二぀の異぀た皮類の繊維を耇合するこ
ずは、埗られた耇合マツトのコスト䜎枛になる。 本発明にかかる䞍織垃は、䞀定の特性がパルプ
繊維によるものであるこずを瀺しおいるが、この
䞍織垃には必らず意味のある量の熱可塑性マむク
ロ繊維が含たれおいる。この結果、ホツト・カレ
ンダ加工、゚ンボス加工、あるいはスポツト接合
などの二次熱凊理をするこずによ぀お、この䞍織
垃を改造するこずが可胜である。 ぀の空気流の混合じよう乱によ぀お皮類の
繊維原料を耇合するこずの付加的な利点は、䞡繊
維原料が党䜓にわた぀お均䞀に分垃しおいる耇合
り゚ツブが埗られるこずである。前述したよう
に、この成果は぀の空気流に本質的な速床差を
䞎えるこずによ぀お達成されるが、速床差が倧き
い皋均䞀な耇合になり、速床差が小さい皋第の
原料の党䜓にわた぀お第の原料が片寄぀お集䞭
する傟向が生じる。もし必芁なずきは、り゚ツブ
平面のどの方向にも䞀様な性質を有する補品を、
゚ンボス加工などにより、り゚ツブの厚さを実質
䞊倉曎するこずなしに䜜るこずができる。 溶融玡糞マむクロ繊維を生成するのに䜿甚でき
る熱可塑性高分子は倚皮倚様であり、高分子又は
それらの組合せを適圓に遞択するこずによ぀お、
いろいろな物理的性質をも぀䞍織垃を䜜るこずが
できる。倚くの有甚な熱可塑性重合䜓のなかで
も、ポリプロピレンやポリ゚チレンなどのポリオ
レフむン系、ポリアミド系、ポリ゚チレンテレフ
タレヌトなどのポリ゚ステル系、およびポリりレ
タン系の熱可塑性゚ラストマヌは、本明现曞に蚘
茉した䞍織垃を補造する際に、も぀ずも広範な甚
途があるものず考えられる。 朚材パルプ繊維を含む二次空気流を䜜るにはむ
しろ図解配眮図に瀺されおいるピツカロヌルの方
が奜たしいが、ステヌプルナむロン繊維などの合
成繊維や、綿、亜麻、ゞナヌト、絹などの倩然繊
維からなる付加的繊維材料および特定の材料又は
その䞀方を含む二次空気流を䜜る堎合には、別の
装眮を䜿甚するこずができる。 もし、必芁があれば、朚材パルプ繊維ずもう
぀の付加材料を぀の二次空気流で搬送するこず
ができる。出来䞊぀た繊維性り゚ツブに䞀定の組
合せ特性を付䞎するための制埡可胜な倉数は、り
゚ツブの成分や坪量のほか、䞀次空気流および二
次空気流の䞡方にいく぀もある。 䞀次空気流における制埡に敏感なプロセスパラ
メヌタには、空気流の枩床600〜700〓の範囲が
望たしい、空気流の速床ダむヘツド内郚で音
速にな぀おいるこずが望たしい、高分子抌出し
速床孔圓り0.25min前埌が望たしい、
高分子の枩床、および空気ず高分子の質量流量比
10〜100の範囲にあるこずが望たし
い、がある。 二次空気流における制埡可胜な倉数は、空気流
量ずピツカ・ロヌルの呚速、空気流の速床亜音
速の範囲内で、50〜250ftsecが望たしい、お
よび繊維長兞型的なもので長さ3.0mm前埌で
ある。又䞀次空気流ず二次空気流ずの関係も制埡
するこずができ、䞀般に䞀次空気流ず二次空気流
の速床比は〜10の範囲にあるこずが望
たしい。䞀次空気流および二次空気流によ぀お導
入される原料の盞察比率は広範囲に倉えるこずが
でき、高分子マむクロ繊維は完成マツトの重量の
〜80が兞型的である。又合流点における䞀
次空気流ず二次空気流のなす角も倉えるこずがで
きるが、䞀般には぀の流れが盞互い盎角で合流
するこずが望たしい。同じように、぀の流れが
合流する特定点も䞊流偎にある溶融玡糞ダむず䞋
流偎にある有孔衚面をも぀ロヌルずに関連しお倉
えるこずができる。 本発明による䞍織垃の補造に぀いお以䞋の諞実
斜䟋で説明する。又各皮の構成成分をも぀お䜜ら
れた䞍織垃の物理的諞特性の枬定結果に぀いおも
蚘茉する。枬定は以䞋述べる方法にしたが぀お実
質的になされた。 (a) 非圧瞮厚さ Cwtom Scientific Instruments瀟補の厚さ
詊隓機を䜿甚し、実斜䟋―に぀いおは
1in2footで0.5oz/in2の圧力を䞍織垃に加え、残
りの実斜䟋に぀いおは7.07in2footで0.004psiの
圧力を䞍織垃に加えた状態で枬定した。 (b) かさ密床 かさ密床(/cm3)は枬定した非圧瞮厚さず既
知の詊料坪量を甚いお蚈算したかさ密床坪
量厚さ。 (c) 油吞収性 平方むンチの詊料に぀いお重さを枬぀た埌
垞枩で30秒間鉱物油に浞け、次に取出し、45秒
間ガラス棒で吊り䞋げ油を切り、再び詊料の重
さを枬぀た。重量増加分が詊料に吞収された油
の重量である。この重量を油の比重0.831/
で割぀お容積を求め、これを詊料の也燥
重量で割぀お「油吞収性」を求めた。 (d) 氎分吞収性 油の代りに氎を䜿぀おいるだけで油吞収性詊
隓ず同様である。詊料党䜓を均䞀にぬらすた
め、第衚および衚の吞収性詊隓では
Aerosol OT界面掻性剀の0.5氎溶液を甚いお
実斜した。 (e) 裂断長 匕匵匷床詊隓は、幅1.0むンチ、長さむン
チの䞍織垃詊料も぀ず長い詊料も䜿甚できる
が、詊隓機のゞペヌの間に露出する長さはむ
ンチであるを䜿い、Instron瀟補の詊隓機
ModelNo.A70で実斜した。枩床70−77〓、盞
察湿床40−50においお、匕匵り速床10in/mi
で詊料に荷重を加え、枬定した匕匵匷床を詊
料の坪量で割぀お裂断長を求めた。湿最裂断長
を枬定する堎合には、詊料を30秒間氎に浞し、
次に吞取玙の䞊にのせ過剰な氎分を陀去した埌
詊隓した。 再也燥裂断長を枬定する堎合は、詊料を前述
したようにぬらし、通気也燥埌詊隓した。 (f) 䌞 床 䞊で述べた匕匵匷床詊隓においお、増加䞭の
詊料の長さを枬定し、詊料が裂断する盎前の詊
料の長さの増加癟分率がその䌞床である。 (g) リント数 共通の立軞䞊に互いにむンチ離しお眮かれ
た二぀の平行内板の呚瞁に平方むンチの詊料
をし぀かり留める。次に内板のひず぀を他の内
板に察しお各ストロヌクで180゜だけ回転する
ように反埩しお動かし、詊料を屈曲させ、捩
り、しわくちやにする。盎埄47mm、孔サむズ
0.45ミクロンのMillipore瀟補のフむルタNo.
HAWP―047―00をその䞭心が二぀の円板の
呚瞁のわずか倖偎にくるようにしお詊料の䞋に
眮き、この円板反埩動䜜を50回続ける。次に倍
率が40倍の顕埮鏡を通しお、フむルタヌ䞊に捕
足された埮粒子をTVカメラずモニタヌで芳察
する。フむルタ䞊の぀の異぀た1.64×2.43mm
の芖域内にある13ミクロン以䞊の埮粒子数をす
べおかぞえる。これら぀の芖域のうち぀は
フむルタの円呚たわりに等間隔にずり、぀は
フむルタの䞭倮にずる。埗られた぀の埮粒子
数の平均を求め、埗られた平均数を「リント
数」ずしお蚘録した。 (h) 比容積 「初期比容積」は非圧瞮厚さcm、䞍織垃に
0.004psiの圧力を加え、7.07in2footを甚いお䞊
蚘方法によ぀お枬定したものを詊料の坪量
/cm2)で割぀お求めた。次に、詊料の衚面䞊均
等に0.49psiの圧力を加え、分埌にこの負荷
の䞋で圧瞮厚さを前述した厚さ詊隓機で枬定
し、埗られた圧瞮厚さを坪量で割぀お、「負荷
時比容積」を求めた。次に、詊料から負荷を取
り陀き、分埌に回埩した詊料の厚さを前述ず
同じ方法で枬定し、非圧瞮厚さを求めた
0.004psiの圧力を加え、7.07in2footを䜿甚す
る、埗られた回埩埌の厚さを坪量で割぀お
「回埩比容積」を求めた。 実斜䟋 53.5の挂癜した亜硫酞パルプ繊維ず46.5の
溶融玡糞のポリプロピレン・マむクロ繊維を含有
する耇合䞍織垃で、第図に瀺した䞀般的補法に
埓぀お䜜぀たものである。たず、最終枩床600〓
のポリプロピレンExxon resin、CD―523を
221bshrダむ・オリフむス圓り0.42/minに
等しいの速床で抌出し、枩床が700〓、流量が
15001bshr、流速が音速の次空気流の䞭で延
䌞した。 浮遊パルプ毛矜を含む次空気流を、ピツカ装
眮の䞭で流量15001bshrの空気を䜿甚しおロヌ
ルパルプRayfluff XQ、平均繊維長が2.1mmの
米囜西郚産の぀が材パルプを解繊しお䜜り、こ
の次空気流をダむの先端から玄むンチの所で
次空気ずポリプロピレンマむクロ繊維の流れに
盎角に合流させた。合流点における次空気流の
速床は抂算で次空気流の速床の−10倍であ぀
た。 そしお抌出しダむの先端から22むンチ離れた所
にあるロヌルニツプの間隙が12.5ミルの金網でカ
バヌした真空ロヌルの間に耇合り゚ツブを集積さ
せた。 䞋蚘は枬定した耇合䞍織垃の特性である。 坪 量 99/m2 非圧瞮厚さ 1.55mm かさ密床 0.064/cm3 油吞収性 18.8ml/ 瞊方向の裂断長 196 瞊方向の䌞床 20 暪方向の裂断長 358 暪方向の䌞床 34 さらに、このり゚ツブはプルト又は服地のよ
うである、圧瞮性があ぀おクツシペンのようであ
る、順応性があり、ごわごわしおいないなどの特
城がある。これらの性質から考えられる可胜性の
ある甚途ずしおは、おむ぀、研磚垃、小さなバン
ド゚むド、メヌキダツプ陀去パツド、理髪および
矎容補助補品がある。さらにこの䞍織垃は非垞に
効果的にほこりなどの小さな単䜓を付着させ、保
持するこずが刀぀たので、ほこりよけカバヌずし
おも有効に䜿甚できるであろう。 この䞍織垃は芪氎性朚材パルプ繊維が重量の倧
半を占めおいるが、氎にぬれ難くい。この性質は
化粧品やパツドの衚面に塗られおいる物質を離隔
するこずが望たしいそのほかの塗垃補品の塗垃甚
パツドに郜合が良い。 実斜䟋 実斜䟋の耇合䞍織垃の䞀郚を、第図に瀺し
た゚ンボス加工暡様の付いたアンビルロヌルに抌
し぀け超音波カレンダ加工によ぀お゚ンボスした
ものである。枬定した特性を以䞋に瀺す。 坪 量 91/m2 厚 さ 0.81mm かさ密床 0.112/cm3 油吞収性 8.8ml/ 瞊方向の裂断長 822 瞊方向の䌞床 36 暪方向の裂断長 444 暪方向の䌞床 26 さらに、この䞍織垃の特城は䟝然服地のような
感じであるが、゚ンボスしおいない実斜䟋の䞍
織垃よりも匷くか぀剛いこずである。又゚ンボス
加工の結果、゚ンボス郚分にある個々のパルプ繊
維の郚分をよりし぀かりず結合させるこずによ぀
お衚面のリントが少ない。 甚途ずしおは、䜿い捚お皿拭垃、耐久性のある
工業甚あるいは家庭甚拭垃、ナプキン、クレンザ
ヌやアストリンれンなどを含たせお甚いるぬれ拭
垃などがある。 実斜䟋 52の繊維状パルプRayflutt XQず48の
溶融玡糞のポリプロピレン繊維Exxonresin、
CD―523を含有する耇合䞍織垃で、り゚ツブ圢
成甚ロヌルニツプから抌し出しダむ端郚たでの距
離が14 7/8むンチである点を陀いお、実斜䟋ず
同じ補法で䜜぀た。枬定した特性を以䞋に瀺す。 坪 量 92.3/m2 厚 さ 0.74mm かさ密床 0.125/cm3 油吞収性 9.7ml/ 瞊方向の裂断長さ 693 瞊方向の䌞床 10 暪方向の裂断長さ 590 暪方向の䌞床 18 この䞍織垃は、実斜䟋の䞍織垃に比べるず、
剛く、目が぀んでいお、順応性が悪く、その感觊
性は服地のようなものよりもこわごわしおおり、
り゚ツブ成圢甚ワむダロヌル衚面でり゚ツブ衚面
に凹凞が付く結果、若干ざらざらした衚面組織ず
な぀おいる。又、氎にぬれ難くい。この䞍織垃は
衣服のむンタヌプヌシングや限定䜿甚の敷きマ
ツトやテヌブルクロスずしお䜿甚するこずができ
るであろう。 実斜䟋 実斜䟋の耇合䞍織垃の䞀郚を、第図に瀺し
た゚ンボス加工暡様の付いたアンビルロヌルに抌
し付け超音波カレンダリングによ぀お゚ンボスし
たものである。枬定した特性を以䞋に瀺す。 坪 量 92.5/m2 厚 さ 0.71mm かさ密床 0.130/cm3 油吞収性 7.2ml/ 瞊方向の裂断長 694 瞊方向の䌞床 22 暪方向の裂断長 644 暪方向の䌞床 27 この䞍織垃はごしごしこす぀たり、すり磚いた
りする甚途に察しおは十分な匷床ず耐久性を有
し、氎にぬれ難くい。この䞍織垃は限定䜿甚の敷
きマツトやテヌブルクロスに䜿甚するこずができ
る。 実斜䟋 47の繊維化パルプRayflutt XQず52.3
のポリプロピレンExxon resin、CD―523溶
融玡糞繊維を含有する耇合䞍織垃で、前述した䞀
般的補法に埓぀お䜜぀たものである。このポリプ
レン暹脂は、抌し出し工皋においお、溶融玡糞繊
維の重量の6.5の界面掻性剀を添加しお倉性さ
せた。この倉性繊維を最終枩床575〓においお、
23lbs/hrの速床で抌し出し、枩床が700〓、流量
が1500lbs/hr、流速が音速の次空気流の䞭で延
䌞した。パルプ繊維の投入ず耇合工皋は実斜䟋
の堎合ず同じである。埗られた䞍織垃は氎にぬれ
易い。枬定した特性を以䞋に瀺す。 坪 量 94.5/m2 厚 さ 1.42mm かさ密床 0.066/cm3 油吞収性 17.9ml/ 瞊方向の裂断長 159 瞊方向の䌞床 39 暪方向の裂断長 168 暪方向の䌞床 63 この䞍織垃は氎にぬれ易いこずを陀いお、実斜
䟋の䞍織垃ずその質が非垞に類䌌しおいるの
で、その朜圚的甚途も類䌌しおいる。 実斜䟋 実斜䟋の耇合䞍織垃の䞀郚を、第図に瀺し
た゚ンボス加工暡様の付いたアンビルロヌルに抌
し付け、超長波カレンダ加工によ぀お、゚ンボス
したものである。枬定した特性を以䞋に瀺す。 坪 量 94/m2 厚 さ 0.71mm かさ密床 0.132/cm3 油吞収性 8.0ml/ 氎分吞収性 6.2ml/ 瞊方向の也燥裂断長 801 〃 〃䌞床 39 暪方向の也燥裂断長 680 〃 〃䌞床 45 瞊方向の湿最裂断長 754 〃 〃䌞床 43 暪方向の湿最裂断長 572 〃 䌞床 48 瞊方向の再也燥裂断長 778 〃 〃䌞床 50 暪方向の再也燥裂断長 649 〃 䌞床 61 この䞍織垃は湿最状態にあるずきも、あるいは
ぬれた状態からの再也燥埌でも、その物理的およ
び機械的性質に倉化はないので、也燥状態ず湿最
状態のいずれでも䜿甚するこずができ、限定䜿甚
の又は耐久性のあるいろいろな圹に立぀拭垃ずし
お朜圚的な甚途をも぀おいる。 実斜䟋 74の繊維化パルプRayfluff XQず26の
ポリプロピレンExxon resin、CD―523溶融
玡糞繊維を含有する耇合䞍織垃で、り゚ツブ成圢
甚ワむダロヌル衚面から抌し出しダむ端郚たでの
距離を30 1/4むンチ、およびワむダロヌルニツプ
の間隙を105ミルにしたこずを陀いお、実斜䟋
ず同じ補法で䜜぀たものである。枬定した特性を
以䞋に瀺す。 坪 量 181/m2 非圧瞮厚さ 4.06mm かさ密床 0.045/cm3 油吞収性 26.8ml/ 瞊方向の裂断長 59 〃 䌞床 24 暪方向の裂断長 139 〃 䌞床 40 この䞍織垃はこのほか、柔かい、かさ高であ
る。圧瞮性があり、クツシペンのようである。幟
分詰綿に䌌おいるなどの特城をも぀おいる。吞収
性が倧きいので、衛生ナプキン、おむ぀、包垯な
どに䜿甚するこずが考えられる。そのほかの甚途
しおは、メヌキダツプ陀去甚パツド、塗垃甚パツ
ド、詰め物、矎容パツド䟋、ブラゞダヌ、理
髪および矎容補助補品、保育補品、装食的䜿甚な
どがある。 実斜䟋 50の広葉暹パルプ繊維ず50の溶融玡糞ポリ
プロピレン・マむクロ繊維を含有する耇合䞍織垃
で、第図に瀺した䞀般的補法に埓぀お䜜぀たも
のである。 ポリプロピレン暹脂Exxon resin、CD―
523、10重量の界面掻性剀を配合したものを
最終枩床を635〓にしおダむオリフむス圓り0.33
/minの速床で抌し出し、党高分子の流量の58
倍の質量流量で流れる枩床690〓の次空気流の
䞭で延䌞した。浮遊パルプ繊維を含む次空気流
を、ピツカ装眮の䞭で剥離甚の空気流は甚いずに
ロヌルパむプ平均繊維長が1.5mmの広葉暹を
解繊しお䜜り、抌し出しダむの先端から玄むン
チのずころで次空気ずポリプロピレン・マむク
ロ繊維の流れに盎角に合流させた。そしお、抌し
出しダむの先端から5.5むンチ離れた金網でカバ
ヌした真空ロヌルの衚面䞊に耇合り゚ツブを集積
させた。枬定した諞特性を以䞋に瀺す。 坪 量 85/m2 厚 さ 1.57mm かさ密床 0.054/cm3 氎分吞収性 15.8ml/ 瞊方向の也燥裂断長 137 〃 〃 䌞床 33 暪方向の也燥裂断長 83 〃 〃 䌞床 59 このり゚ツブは氎にぬれ易く、又極めお゜フト
な感觊のものである。ドレヌプ性は䞊蚘した諞り
゚ツブず同じであるが、も぀ず柔かな衚面組織を
も぀おいる。 実斜䟋 50の西掋杉パルプ繊維ず50の溶融玡糞ポリ
プロピレン・マむクロ繊維を含有する耇合䞍織垃
で、実斜䟋ず同じ補法で䜜぀たものである。パ
ルプ繊維を含む次空気流は平均繊維長が3.9mm
のCedanier瀟補のロヌルパルプを解繊しお䜜぀
た。枬定した諞特性を以䞋に瀺す。 坪 量 83/m2 厚 さ 1.77mm かさ密床 0.047/cm3 氎分吞収性 18.9ml/ 瞊方向の也燥裂断長 119 〃 〃 䌞床 26 暪方向の也燥裂断長 60 〃 〃 䌞床 46 このり゚ツブは氎にぬれ易い。 超音波カレンダ加工を斜した䞊蚘の各実斜䟋に
おいお䜿甚した装眮は、前に述べたBranson瀟補
の装眮で、ホヌン䞊で50psiに蚭定し、り゚ツブ
通過速床を211ft/minにしお䜿甚した。 第図―第図は以䞋の補法で䜜぀た䞍織垃の
走査電子顕埮鏡写真である。本䞍織垃は50.4の
軟質朚材パルプ繊維Longlac―18、平均繊維長
が3.2mmのずうひず束のパルプず49.6の溶融
玡糞ポリプロピレン繊維Exxon resin、CD―
392を含有した耇合䞍織垃である。この䞍織垃
は、浮遊しおいる朚材パルプ繊維を搬送する次
空気流を、高枩空気ず溶融玡糞ポリプロピレン繊
維を含む次空気流に盎角に向けおダむ端郚から
玄むンチの所で合流させお䜜぀たものである。
溶融玡糞繊維はポリプロピレン暹脂を最終枩床を
630〓にしお、ダむオリフむス圓り0.31/minの
速床で抌し出しお生成し、党高分子流量の66.1倍
の質量流量で流れる枩床690〓の次空気流の䞭
で抌し出された玡糞を延䌞した。次空気流は、
察の䟛絊ロヌルを介しお朚材パルプ繊維からな
るカヌドり゚ツブをり゚ツブの反察偎に配眮され
た察のノズルからなるフアむバヌガンに送り蟌
むこずによ぀お䜜぀た。すなわち、ノズルから出
る高速の空気ゞ゚ツトでカヌドり゚ツブを個々の
繊維に解きほぐしお繊維を高速気流の䞭に投入
し、この繊維流をダクトで導き、溶融玡糞繊維の
次空気流に合流させ、抌し出しダむ端郚から
5.5むンチ離れた金網でカバヌされた真空ロヌル
の衚面の䞊に耇合り゚ツブを集積させた。 第図80倍は、耇合繊維組織の均䞀性、繊
維方向のランダム性、パルプ繊維ず溶融玡糞繊維
の党䜓的な絡み合い、䞡繊維の盞察的な盎埄など
を瀺しおいる。第図300倍は、さらにパル
プ繊維を溶融玡糞マむクロ繊維の党䜓的な絡み合
い、繊維の盞察的寞法、り゚ツブ内の倧きな空間
などを瀺しおいる。第図1000倍は、倚数の
マむクロ繊維の絡み合いによ぀お支持されたパル
プ繊維の䞀郚分を瀺す。溶融玡糞繊維の盎埄の偏
差は兞型的なもので―ミクロンである。り゚
ツブ内でのポリプロピレン繊維間の結合は倚くは
ないが、写真からわかるように、倧きな盎埄の繊
維ず異぀たサむズの繊維ずの結合が起きおいる
本写真の堎合は、盎埄玄14ミクロンの繊維ず玄
ミクロンの繊維間の結合である。この皮の結
合はかさ高で䜎密床り゚ツブにおいおはたれであ
り、り゚ツブの圢状保持性の䞻芁な基瀎はパルプ
繊維ず溶融玡糞マむクロ繊維の双方の広範囲な物
理的絡み合いにあるこずは明らかである。ポリプ
ロピレン繊維ずセルロヌズパルプ繊維ずの結合は
芋぀からなか぀た。このように繊維間結合がない
こずが、䜎密床り゚ツブにすばらしい柔らかさず
可撓性ずドレヌプ性を付䞎しおいるのである。 衚面および内郚共その組織が均䞀であるため、
䞍織垃は合成暹脂のマむクロ繊維ずパルプ繊維の
䞡方の特性を瀺す。䟋えば、倧郚分がパルプ繊維
である耇合䞍織垃であ぀おも、衚面の䜎衚面゚ネ
ルギヌのマむクロ繊維の存圚がその湿最性を制限
しおいる。又、り゚ツブ党䜓にわた぀お熱可塑性
繊維が分垃しおいるため、カレンダ加工やスポツ
ト結合や他の熱可塑性り゚ツブ又はフむルムぞの
積局などの加工を通じお、熱的にり゚ブ構造を改
造するこずが可胜にな぀た。 第図―第図は以䞋の点を陀いお䞊述した
方法ず同䞀の補造で䜜぀た䞍織垃の走査電子顕埮
鏡写真である。すなわち、本䞍織垃は48.5の軟
質朚材パルプ繊維Longlac―18、平均繊維長が
3.2mmのずうひず束のパルプず51.5の溶融玡
糞ポリプロピレン繊維Exxon resin、CD―
392を含有し、ダむオリフむス圓りの抌し出し
速床を0.28/minずし、700〓の次空気ず665
〓の高分子の質量流量の比を85にしお䜜぀た
もので、さらに第図ず第図に瀺した゚ンボス
加工暡様を有するアンビルロヌルに抌し付けお超
音波カレンダヌ加工をし、高密床化したものであ
る。再び第図600倍ず第図600倍
に、り゚ツブは高密床にはな぀おいるが゚ンボス
されおいない郚分にある溶融玡糞マむクロ繊維ず
パルプ繊維の党䜓的な絡み合いを瀺す。第図
300倍は匷力なカレンダ加工によ぀お圢成され
た、第図の凹郚に盞圓する゚ンボス郚分を
瀺しおいる。 この゚ンボス郚分では熱可塑性繊維の繊維構造
は倱われおおり、結果ずしお生じたフむルムがパ
ルプ繊維をその䜍眮にし぀かり保持する圹目をし
おいる。このような方法で兞型的なカレンダヌ加
工を斜した䞍織垃は、匕匵匷さず密床が増し、液
䜓吞収性は䜎䞋したが液䜓導通性は高た぀おい
る。 疎氎性で氎に匷い繊維が存圚するため、耇合䞍
織垃は氎や氎溶媒の䞭では安定性がある。そのほ
か、ポリオレフむン系繊維は油や溶剀に察する吞
収性を高める。溶融玡糞マむクロ繊維の母䜓の䞭
にパルプ繊維が組み蟌たれおいる結果、かさ高性
が増し、空間のある構造にな぀おいる。 パルプ繊維ずマむクロ繊維が党䜓的に絡み合぀
おいるため、党䜓の耇合構造は良奜な圢状保持性
ず耐磚性を有し、もし必芁であれば、り゚ツブ構
造を安定化するため、接着剀の䜿甚は容易にでき
るけれども、この耇合䞍織垃では接着剀は䞍芁で
ある。 実斜䟋  次頁の第衚にそれぞれ類別されおいる぀の
詊料に぀いおの぀のシリヌズは、瀺されおいる
ようにマむクロ繊維察朚材パルプ繊維比を広範囲
にず぀お構成されおいる。マむクロ繊維は各シリ
ヌズに察しお瀺されおいる速床ず枩床でポリプロ
ピレン暹脂Hercules PC 973を抌し出しお生
成した。次空気の速床はどの堎合にも830―
1390ft/secの範囲で亜音速であ぀たが、空気枩床
は665〓ず䞀定にした。浮遊パルプ毛矜を含有す
る次空気流は、ピツカヌ装眮の䞭で初期速床77
ft/sec流量玄14401bs/hrの空気流を䜿぀お、ロ
ヌルパむプRayfloc XJ.平均繊維長玄3.0mmの南
郚産束のパルプを解繊しお䜜぀た。耇合り゚ツ
ブは抌出しダむの先端から7.5むンチのずころに
ある個の有孔真空ロヌル䞊に集積させた。 シリヌズないしシリヌズに察しお、枬定し
た耇合䞍織垃の諞特性を、Rayfloc XJの100パ
ルプの空気圢成の詰綿のデヌタず共に、第衚に
たずめお瀺す。
The present invention relates generally to nonwoven fabrics, including wood pulp fibers and thermoplastic polymer microfibers, which can be manufactured inexpensively and in a number of different combinations of properties for different applications. Regarding nonwoven fabrics. It is the object of the present invention to obtain an improved non-woven fabric that can be produced quickly and inexpensively in a single manufacturing step without the use of adhesives or the need for embossing or other treatments after the formation of the non-woven fabric. It is a purpose. It is also an object of the present invention to obtain an improved nonwoven fabric in which wood pulp fibers and polymeric fibers are co-ordinated and the final product has the desired combination of properties. It is also a related purpose to manufacture It is an object of one aspect of the present invention to obtain an improved nonwoven fabric with a unique combination of tensile strength, absorbency, and hand, having high absorbency while having wet strength comparable to dry strength. It is one of the objectives of one embodiment of the present invention to obtain a nonwoven fabric that exhibits high properties. It is also an object of the present invention to provide an improved nonwoven fabric that is highly elastic, ie, has the ability to recover from deformation, has a low bulk density, and can be manufactured at relatively low cost. It is also an object of the present invention for specific applications to provide improved nonwoven fabrics that have high absorbency for both oil and water. It is also an object of the present invention to obtain an improved nonwoven fabric in which there is little or no mutual bonding of the wood pulp fibers even after drying after wetting, and the original properties of the nonwoven fabric are well retained. In this connection, it is also a related object of the present invention to obtain a nonwoven fabric whose original physical structure remains almost unchanged even after drying after wetting. It is also an object of the present invention to obtain a process for producing a nonwoven fabric having a relatively large bulk per unit weight. Another object of the present invention is to provide a process for producing a nonwoven fabric using only air without wetting the components of the nonwoven fabric. Although the invention will now be described with reference to specific embodiments, it should be understood that the invention is not limited to these embodiments. On the other hand, all alternatives, modifications, and equivalents that can be included within the scope and spirit of the invention as defined in the claims are to be included in the present invention. Now, to explain according to the drawings, first of all, in FIG.
technique). This method is
Industrial and Engineering Chemistry
Published in Vol.48, No.8, pp1342-1346, USA
It is the same as described in a paper entitled "Superfine Thermoplastic Fibers" which describes research at the Naval Research Laboratory. Additionally, Naval Research
See also Report 111437 (issued April 15, 1954) and US Pat. No. 3,676,242 (issued July 11, 1972). The basis of this molding method is to extrude a molten polymer raw material into a thin stream through a die head 11, and stretch the polymer stream by a contracting flow of high-speed, high-temperature gas (usually air) sent from nozzles 12 and 13. It is then blown off into discontinuous microfibers of minute diameter. It is desirable that the die head is provided with at least one row of a plurality of closely spaced extrusion holes. Microfibers formed in this manner generally have an average diameter of no more than 10 microns, and rarely exceed 10 microns in diameter. The average diameter of the microfibers is usually about 1 micron or greater, preferably in the range of 2 to 6 microns, with an average diameter of about 5 microns. It should be noted here that although most of the microfibers are discontinuous, they have a fiber length longer than what is generally called staple fiber. The primary air stream 10 is combined with a secondary air stream containing defibrated wood pulp fibers to combine two different fiber raw materials in a single step. The length of a typical defibrated wood pulp fiber is approx.
0.5 to 10 mm, and the ratio of length to maximum width is approximately 10/
1 to 400/1. Its typical cross section is irregular with a width of 30 microns and a thickness of 5 microns. Secondary air flow 14 shown in this schematic layout
is made by a pulp sheet defibration apparatus of the type described and claimed in Assignee's US Pat. No. 3,793,678, "Pulp Picking Apparatus with Improved Fiber Forming Duct." This equipment is used for pulp and
It consists of a conventional picker roll 20 with picker teeth for defibrating the sheet 21 into individual fibers, and the pulp sheet 21 is fed radially onto the picker roll 20 by a feed roll 22. As the picker roll teeth break up the pulp sheet 21 into individual fibers, the separated fibers are conveyed downwardly through the forming nozzle or duct 23 and into the primary air stream. The housing 24 covers the picker roll 20 and provides a passage 25 between the housing 24 and the picker roll 20. From the duct 26, a sufficient amount of process air is supplied through the passage 25 to the picker roll at a speed close to the circumferential speed of the picker teeth to serve as a transport medium for the fibers passing through the forming duct 23. The air can be delivered by conventional means, such as a blower. To avoid agglomeration of the fibers, the individual fibers should be allowed to travel through the duct 23 at approximately the same speed as they leave the picker teeth after being defibrated from the pulp sheet 21. That is, the fiber should vary both in velocity and in its direction at the point of leaving the picker tooth. In particular, it is desirable that the speed of the fibers defibrated from the pulp sheet 21 in the duct 23 does not change by more than about 20%. This is a significant difference compared to other defibrating devices where the flow separation does not allow the fibers to move in an orderly manner from the picker, resulting in a fiber speed change of more than 100% during the journey. In order to maintain the desired fiber speed, the duct 23 is positioned such that its longitudinal axis is substantially parallel to the plane tangent to the picker roll 20 and the fibers are not affected by the picker teeth. Since the duct 23 is in this direction, due to the collision of the fibers on the duct wall,
Fiber velocity remains unchanged. Thus, if the pulp sheet 21 is fed radially toward the picker in a plane substantially parallel to the primary air flow, the surface in contact with the picker roll 20 at the contact point of the pulp sheet is 1 Next, it will be perpendicular to the airflow. Therefore, in the case of the embodiment shown in FIG. 1, the contact point between the sheet and the picker is also the point at which the defibrated fibers are released from the influence of the picker teeth, so the vertical axis of the duct 23 is the primary axis. perpendicular to the airflow 10. However, if the speed of the fibers is restricted due to the influence of the picker teeth after being separated from the pulp sheet 21, the axis of the duct 23 is adjusted appropriately so that it is in the direction of the fiber speed at the point where the fibers are no longer restricted. As shown in FIG. 1, the width of the duct is approximately equal to the height of the picker teeth of roll 20, and the passage between the picker teeth and picker roll housing 24 is very narrow. Because the width of the duct is like this,
The velocity of the process air supplied through duct 26 remains substantially constant both when moving with the picker and through duct 23. Moreover, since the velocity of the processing air is close to that of the picker teeth, and this velocity is essentially the same as the velocity of the defibrated fibers,
Processing air does not cause fiber velocity changes in the duct 23. Given that the width of the duct is approximately the same as the height of the picker teeth, for example less than about 1.5 times the height of the teeth, the air velocity in the duct 23 of the illustrated device will be at least 70% of the circumferential velocity of the picker teeth. Become. The length and width of the duct (width along the picker roll axis) are also important for optimizing wave formation. Preferably, the length of the duct should be as short as the overall equipment design allows. In the case of the device shown in FIG. 1, the minimum duct length is limited by the radius of the picker roll. In order to maintain a constant width of the web formed, the width of the duct should preferably be less than or equal to the width of the pulp sheet fed to the picker rolls. Returning again to the device shown in FIG. 1, it is desirable that the picker teeth used be relatively tall, for example 1/4 inch or larger. This height allows the use of wide ducts, so that the fibers are not interfered with by the walls. As shown in FIG. 1, primary airflow 10 and secondary airflow 14 preferably move at right angles to each other at their confluence. Other convergence angles can be used if necessary. The velocity of the secondary air stream 14 is significantly lower than the primary air stream 10 so that the composite stream 15 created by the merging flows continuously in the same direction as the primary air stream 10.
Combining the two air streams is somewhat similar to an aspirator effect, with fibers in the secondary air stream 14 being sucked into the primary air stream as they pass through the outlet of the duct 23. In any case, the important thing is that the primary air flow and the secondary air flow merge in a turbulent state,
A speed difference was provided between the two air streams to ensure complete mixing of the pulp fibers in the secondary air stream and the melt-spun microfibers in the primary air stream. In general, increasing the velocity difference between the primary and secondary air streams will result in a more uniform mixing of the two feedstocks;
If the two flow velocities are slow and the speed difference is small, the components tend to be mixed. To maximize production speed, it is generally desirable to have the primary air flow at an initial sonic velocity (in nozzles 12 and 13) and the secondary air flow at or below the sonic speed.
Naturally, the primary air stream expands with decreasing velocity as soon as it leaves the nozzles 12,13. The flow rate of the primary air that entrains surrounding air while drawing the polymeric microfibers is always greater than the flow rate of the secondary air used to introduce the pulp fibers. The primary air jet increases in volumetric flow rate by more than five times while the maximum jet velocity decreases to 20% of its original value. However, the pulp fibers should be introduced at the beginning of the diffusion zone of this microfiber jet. This is because it exposes the mixture of both fibers to the strong micro-turbulence occurring in this part of the diffusion zone and mixes both fibers while the polymeric microfibers are still in their hot and soft nascent state. be. Behind the diffusion zone of the microfiber jet, the magnitude of the disturbance becomes larger compared to the fiber entanglement, and the energy in the disturbance also decreases continuously. This extremely strong small disturbance field causes the short pulp fibers to be mechanically incorporated into the microfiber matrix in the best possible manner. As the velocity of the high velocity air stream carrying the microfibers decreases, the fibers are released from the suction forces that originally created the microfibers from the polymeric melt. When the microfibers relax, they are able to follow small vortices well enough to disperse into the gaseous medium,
While floating, it entangles with relatively short wood pulp fibers, trapping and restraining them. The resulting product is a tightly bonded mixture of wood pulp fibers and polymeric microfibers, which are composited by physically capturing and mechanically entangling them while floating in space. It is desirable to begin this combination operation while the microfibers are still in their hot, soft, nascent state. The microfibers are drawn either before or after their entanglement with the wood pulp fibers. The amount of stretching is from about 3.8 microns (0.015 inch) fiber diameter (a typical extrusion hole diameter) to about 5 microns (0.0002 inch) or less. Most stretching occurs within about 3 inches of the die end face before the primary air velocity drops below about 250 feet per second. Since the wood pulp fibers are introduced into the microfiber stream approximately 1 inch from the die end face, drawing of the microfibers continues after merging with the wood pulp fibers. Because of their extremely small cross-sectional area, polymeric microfibers are at least as small as traditional textile fibers made from the same polymers.
It is 50 to 100 times more flexible, and is very flexible and malleable in its initial state of formation at high temperatures. Microfibers are significantly longer, thinner, limp, and more flexible than wood pulp fibers;
As soon as the two fiber streams meet, they twist and wrap around the relatively short, thick, and stiff wood pulp fibers. This entanglement creates a strong and connective fiber-to-fiber bond, interconnecting two different types of fibers, without any adhesive, molecular or hydrogen bonds. Within this matrix, the microfibers have great flexibility with many microfibers spaced apart by intertwining with relatively stiff pulp fibers. When various types of torsional force are applied to this matrix, the entangled pulp fibers can freely change their direction, but it is the microfibers that return the pulp fibers to their original position after the torsional force is removed. These are the elasticity and repulsive force of the net. The tightly bonded composite fiber structure is formed solely by the mechanical entanglement and mutual bonding of these two different fibers. The microfibers themselves and the anchoring structure to the wood pulp fibers provide a bending hinge between the fibers of the product structure. The fibers are not rigidly bonded to each other, and at their bond points the fibers can rotate, twist, and bend. With an appropriate microfiber content, this fibrous system can have a woven-like "hand" and drape, and can be made malleable while retaining some elasticity and resilience. This structure also exhibits deflection resiliency and wet strength comparable to dry strength, even when wet with water and the wood pulp fibers swell and soften. Even when the microfiber content is as low as 1% by weight, this wood pulp fiber containing structure results in a greatly improved absorbent nonwoven fabric. For example, such nonwoven fabrics have improved shape retention and lower lint counts compared to nonwoven fabrics made by conventional methods that also contain a high content of wood bulp fibers. This wood pulp fiber content structure and the other characteristics described above are achieved by air forming the nonwoven fabric without adhesives or any other processing or treatment. Nonwoven fabrics that use adhesives to incorporate wood pulp fibers are not flexible and have low absorption capacity and absorption rate, which is a significant difference compared to this improved nonwoven fabric. The spatial extent of the wood pulp fibers requires a relatively high level of microfiber content. Pulp fibers maintain their shape under the forces of microfiber flow and high temperatures without melting or undergoing any substantial structural changes, thereby physically interfering with polymer-to-polymer interactions. This suggests that the breaking length or tensile strength increases unexpectedly at very low levels of microfiber content;
Thereafter, there is an unexpected change in the strength of the microfiber web, as evidenced by a drop below the straight line of strength versus microfiber content. To achieve a homogeneous texture, it is preferred that the wood pulp fibers be uniformly distributed throughout the microfiber matrix. Wood pulp fibers have been found to reduce the undesirable effects of "shot" or polymer agglomeration that are inherent in most microfiber spinning processes. With a web made of 100% microfiber,
These polymer aggregates easily fuse with each other and with nearby microfibers, making the web rough to the touch, stiff, and unsightly. Wood pulp fibers have the effect of eliminating the "shot" in both texture and appearance by interfering with the bonding of "shot" molecules with each other and with the microfibers. To form the mixed fibers in composite stream 15 into a composite fiber mat or web, a pair of vacuum rolls 30 and 31 having perforated surfaces are continuously rotated over a pair of stationary vacuum nozzles 32 and 33. Pass this stream 15 through the nip. When the composite stream 15 enters the nip between rolls 30 and 31, the mixed fibers pass through the two rolls 3
0 and 31 and is slightly compressed, while the entire conveyance is sucked into two vacuum nozzles 32 and 33. In this way, the more you can pull out of the nip of the vacuum roll, the more
A web 34 made of self-supporting composite fibers having sufficient shape retention is formed and sent to a winding roll 35. Web 34 wound on roll 35
is shown in Figure 2. The structure of the wood pulp fibers in the composite fiber matrix and the other characteristics described above are obtained without any processing or treatment of the air-infused web. If it is necessary to increase the strength of the composite web 34, it can be embossed using either ultrasound or high temperature to flatten the thermoplastic microfibers within the embossments into a film-like structure. This film-like structure, described in more detail below with respect to FIG. 11, serves to rigidly support the wood pulp fibers in position within the embossments.
In the process of FIG. 1, the composite web 34 passes through an ultrasonic embossing section consisting of an ultrasonic calendering head 40 which is vibrated against a patterned anvil roll 41. The embossing pattern as well as the embossing conditions (eg, pressure, speed, input power) can be appropriately selected to impart desired properties to the final product. After passing through the embossing nip, the web has an embossed area that is approximately 5% to 50% of the surface area of the nonwoven fabric, and a density of individual embossed areas that is approximately 5% to 50% of the surface area of the nonwoven fabric.
It is desirable that a discontinuous pattern of 7.7 to 15.5/cm 2 (50-100/in 2 ) is applied. The most appropriate embossing conditions for a given nonwoven fabric will vary depending on the individual constituent fibers. As a thermoplastic polymer for microfibers,
For nonwoven fabrics made from polypropylene, a Branson ultrasonic device (Model 460) with a continuous ultrasonic module was used with an input power of 700 watts and a 10"
50psi pressure on 0.5″ ultrasonic horn,
It has been found that by pressing against a patterned anvil roll 41, the strength of this nonwoven fabric can be substantially improved. Suitable patterns for anvil rolls are shown in FIGS. 3-5. A suitable speed for the web to pass through the embossing section is 25-150 ft/min. One of the main advantages of the present invention is that it takes advantage of all the advantages of the melt-spinning process, and at the same time, by combining the melt-spun-produced microfibers with varying amounts and types of wood pulp fibers, It becomes possible to impart various desired combinations of properties to the final product that cannot be achieved using the spinning process alone. As a result, using this manufacturing process,
It is possible to produce a variety of specially tailored nonwoven fabrics for various uses. For example, polymeric microfiber mats can be produced efficiently at high speeds by melt spinning, but these mats have limited liquid retention and absorbency;
It is generally not suitable for use as a wiping cloth. However, by using the manufacturing process of the present invention, microfibers made by melt spinning are combined with wood pulp fibers, and the liquid holding and absorbing properties of pine can be used as a wiping cloth. It can be improved to a level that is suitable even for Furthermore, since wood pulp fibers are often cheaper and more readily available than the polymeric materials from which microfibers are made, combining two different types of fibers reduces the cost of the resulting composite mat. become. Although the nonwoven fabrics of the present invention show that certain properties are due to pulp fibers, the nonwoven fabrics necessarily contain a significant amount of thermoplastic microfibers. As a result, it is possible to modify this nonwoven fabric by performing secondary heat treatments such as hot calendering, embossing, or spot bonding. An additional advantage of compounding two types of fiber materials by mixing and turbulence of two air streams is that a composite web is obtained in which both fiber materials are uniformly distributed throughout. . As mentioned above, this result is achieved by providing a substantial velocity difference between the two air streams; the larger the velocity difference, the more uniform the composite, and the smaller the velocity difference, the more the first feedstock will be mixed. There is a tendency for the second raw material to be concentrated throughout. If necessary, a product with uniform properties in all directions of the web plane may be used.
By embossing or the like, the thickness of the web can be made without substantially changing it. There is a wide variety of thermoplastic polymers that can be used to produce melt-spun microfibers, and by appropriate selection of the polymers or combinations thereof,
Nonwoven fabrics with various physical properties can be made. Among the many useful thermoplastic polymers, thermoplastic elastomers based on polyolefins such as polypropylene and polyethylene, polyamides, polyesters such as polyethylene terephthalate, and polyurethanes are used in producing the nonwoven fabrics described herein. It is thought that it has a wide range of uses. Although Pitzcarole, as shown in the illustrated layout, is preferred for creating a secondary air stream containing wood pulp fibers, synthetic fibers such as staple nylon fibers and natural fibers such as cotton, flax, jute, and silk can be used. Other equipment can be used to create a secondary air stream that includes additional fibrous materials and/or specified materials. If necessary, add wood pulp fiber and another
Two additional materials can be conveyed in one secondary air stream. There are a number of controllable variables, both primary and secondary airflow, as well as web composition and basis weight, to impart a certain combination of properties to the resulting fibrous web. Process parameters that are sensitive to control in the primary air flow include air flow temperature (preferably in the 600-700° range), air flow velocity (preferably at sonic speed inside the die head), and polymer extrusion rate. (preferably around 0.25g/min per hole),
There are the temperature of the polymer and the mass flow ratio of air and polymer (preferably in the range of 10/1 to 100/1). The controllable variables in the secondary airflow are the air flow rate and circumferential speed of the Pitzka roll, the velocity of the airflow (in the subsonic range, preferably 50-250 ft/sec), and the fiber length (typical The length is around 3.0mm). The relationship between the primary air flow and the secondary air flow can also be controlled, and it is generally desirable that the velocity ratio between the primary air flow and the secondary air flow be in the range of 5/1 to 10/1. The relative proportions of raw materials introduced by the primary and secondary air streams can vary over a wide range, with polymeric microfibers typically ranging from 1% to 80% of the weight of the finished mat. Although the angle between the primary and secondary air flows at the meeting point can also be varied, it is generally desirable for the two flows to meet at right angles to each other. Similarly, the particular point at which the two streams meet can also vary with respect to the upstream melt spinning die and the downstream roll with a perforated surface. The production of nonwoven fabrics according to the invention is illustrated in the following examples. The results of measuring the physical properties of nonwoven fabrics made with various constituent components are also described. Measurements were made essentially according to the method described below. (a) Uncompressed thickness Using a thickness tester manufactured by Cwtom Scientific Instruments, for Example-X
Measurements were made with 0.5 oz/in 2 of pressure applied to the nonwoven at 1 in 2 foot, and 0.004 psi of pressure applied to the nonwoven at 7.07 in 2 foot for the remaining examples. (b) Bulk density Bulk density (g/cm 3 ) was calculated using the measured uncompressed thickness and known sample basis weight (bulk density = basis weight/thickness). (c) Oil absorption After weighing a 4 square inch sample, it was immersed in mineral oil for 30 seconds at room temperature, then taken out, suspended with a glass rod for 45 seconds to drain the oil, and the sample was weighed again. . The weight increase is the weight of oil absorbed by the sample. Substitute this weight for the specific gravity of the oil (0.831g/
me) to determine the volume, which was then divided by the dry weight of the sample to determine the "oil absorbency." (d) Water absorption The test is the same as the oil absorption test except that water is used instead of oil. In order to uniformly wet the entire sample, in the absorption tests shown in Tables 1 and 2,
It was performed using a 0.5% aqueous solution of Aerosol OT surfactant. (e) Breaking length Tensile strength tests are performed on nonwoven fabric samples with a width of 1.0 inches and a length of 3 inches (longer samples can also be used, but the exposed length between the jaws of the testing machine is 3 inches). The tests were conducted using an Instron testing machine (Model No. A70). At temperature 70-77〓, relative humidity 40-50%, tensile speed 10in/mi
A load was applied to the sample at n, and the measured tensile strength was divided by the basis weight of the sample to determine the fracture length. To measure wet tear length, soak the sample in water for 30 seconds,
The sample was then placed on blotting paper to remove excess water and tested. When measuring redry tear length, samples were wetted as described above and tested after air drying. (f) Elongation In the tensile strength test described above, the increasing length of the sample is measured, and the elongation is the percentage increase in the length of the sample just before the sample breaks. (g) Lint Count Clamp a 6 inch square sample around the periphery of two parallel inner plates placed 4 inches apart from each other on a common vertical axis. One of the inner plates is then moved repeatedly, rotating 180 degrees with each stroke, relative to the other inner plate, bending, twisting, and crumpling the specimen. Diameter 47mm, hole size
0.45 micron Millipore filter (No.
HAWP-047-00) was placed under the sample so that its center was slightly outside the periphery of the two disks, and this disk repeating motion was continued 50 times. Next, the particles captured on the filter are observed through a microscope with 40x magnification using a TV camera and monitor. 9 different 1.64×2.43mm on filter
Count all particles larger than 13 microns within the visual range. Eight of these nine viewing zones are equally spaced around the circumference of the filter, and one at the center of the filter. The average number of the nine particles obtained was determined, and the obtained average number was recorded as the "lint number". (h) Specific volume “Initial specific volume” is the uncompressed thickness (cm,
It was determined by dividing the sample's basis weight (g/cm 2 ) by the basis weight (g/cm 2 ) of the sample. Next, a pressure of 0.49 psi was applied evenly over the surface of the sample, and after 1 minute, the compressed thickness was measured under this load using the thickness tester described above, and the obtained compressed thickness was divided by the basis weight. , the "specific volume under load" was determined. The load was then removed from the sample, and after 1 minute the recovered sample thickness was measured in the same manner as described above to determine the uncompressed thickness (applying 0.004psi of pressure and using a 7.07in 2 foot). The "recovery specific volume" was calculated by dividing the obtained thickness after recovery by the basis weight. EXAMPLE A composite nonwoven fabric containing 53.5% bleached sulfite pulp fibers and 46.5% melt-spun polypropylene microfibers was made according to the general process shown in FIG. First, the final temperature is 600〓
Polypropylene (Exxon resin, CD-523)
Extrusion at a rate of 221bs/hr (equal to 0.42g/min per die orifice), temperature 700〓, flow rate
It was stretched in a primary air flow of 15001 bs/hr and the flow velocity was sonic. A secondary air flow containing floating pulp fluff is used to defibrate roll pulp (Rayfluff This secondary air stream was created by joining the primary air and polypropylene microfiber streams at right angles approximately 1 inch from the die tip. The velocity of the primary airflow at the confluence point was estimated to be 5-10 times the velocity of the secondary airflow. The composite web was then assembled between vacuum rolls covered with wire mesh with a 12.5 mil roll nip gap 22 inches from the tip of the extrusion die. The following are the properties of the composite nonwoven fabric that were measured. Basis weight 99g/ m 2Uncompressed thickness 1.55mm Bulk density 0.064g/cm 3Oil absorption 18.8ml/g Longitudinal breaking length 196m Longitudinal elongation 20% Lateral breaking length 358m Elongation: 34% In addition, this web has the characteristics of being felt or cloth-like, compressible and cushion-like, flexible and not stiff. Possible uses for these properties include diapers, polishing cloths, small Band-Aids, makeup removal pads, hairdressing and beauty aid products. Furthermore, it has been found that this nonwoven fabric very effectively attaches and retains small particles such as dust, so it could be effectively used as a dust cover. Although most of the weight of this nonwoven fabric is made up of hydrophilic wood pulp fibers, it is difficult to get wet with water. This property is advantageous for application pads for cosmetics and other application products where it is desirable to isolate substances applied to the surface of the pad. Example A part of the composite nonwoven fabric of Example was pressed against an anvil roll with an embossed pattern shown in FIG. 5 and embossed by ultrasonic calendering. The measured characteristics are shown below. Basis weight 91g/ m2 Thickness 0.81mm Bulk density 0.112g/ cm3 Oil absorption 8.8ml/g Longitudinal breaking length 822m Longitudinal elongation 36% Lateral breaking length 444m Lateral elongation 26% Additionally, this nonwoven fabric, while still having a cloth-like feel, is stronger and stiffer than the non-embossed example nonwoven fabric. Embossing also results in less surface lint by more tightly bonding the individual pulp fiber sections in the embossed areas. Applications include disposable dish wipes, durable industrial or household wipes, napkins, and wet wipes impregnated with cleansers, astrins, and the like. Example 52% fibrous pulp (Rayflutt XQ) and 48% melt spun polypropylene fiber (Exxonresin,
A composite nonwoven fabric containing CD-523) was manufactured using the same manufacturing method as in Example, except that the distance from the web forming roll nip to the end of the extrusion die was 14 7/8 inches. The measured characteristics are shown below. Basis weight 92.3g/m 2Thickness 0.74mm Bulk density 0.125g/cm 3Oil absorption 9.7ml/g Longitudinal tear length 693m Longitudinal elongation 10% Lateral tear length 590m Lateral direction Elongation of 18% This nonwoven fabric has a
It is stiff, blind, and has poor adaptability, and its texture is stiffer than that of clothing.
As a result of the unevenness formed on the surface of the web by the surface of the wire roll for forming the web, the surface texture is slightly rough. Also, it is difficult to get wet. This nonwoven fabric could be used as a garment interfacing or as a limited use mat or table cloth. Example A part of the composite nonwoven fabric of Example was pressed against an anvil roll with an embossed pattern shown in FIG. 5 and embossed by ultrasonic calendering. The measured characteristics are shown below. Basis weight 92.5g/m 2Thickness 0.71mm Bulk density 0.130g/cm 3Oil absorption 7.2ml/g Longitudinal breaking length 694m Longitudinal elongation 22% Lateral breaking length 644m Lateral elongation 27% This nonwoven fabric has sufficient strength and durability for scrubbing and polishing applications, and is resistant to water. This nonwoven fabric can be used for limited use mats and tablecloths. Example 47% fiberized pulp (Rayflutt XQ) and 52.3%
This is a composite nonwoven fabric containing polypropylene (Exxon resin, CD-523) melt-spun fibers, made according to the general manufacturing method described above. The polyprene resin was modified during the extrusion process by adding 6.5% of the weight of the melt-spun fibers as a surfactant. This modified fiber is heated to a final temperature of 575〓,
It was extruded at a rate of 23 lbs/hr and stretched in a primary air flow at a temperature of 700 ㎓, a flow rate of 1500 lbs/hr, and a flow velocity of sonic. The input of pulp fibers and the compounding process are the same as in the example. The obtained nonwoven fabric is easily wetted by water. The measured characteristics are shown below. Basis weight 94.5g/m 2Thickness 1.42mm Bulk density 0.066g/cm 3Oil absorption 17.9ml/g Longitudinal breaking length 159m Longitudinal elongation 39% Lateral breaking length 168m Lateral elongation 63% This nonwoven fabric is very similar in quality to the nonwoven fabric of the example, except that it is easily wetted by water, so its potential uses are also similar. Example A part of the composite nonwoven fabric of Example was pressed against an anvil roll with an embossed pattern shown in FIG. 5, and embossed by ultra-long wave calendering. The measured characteristics are shown below. Basis weight 94g/m 2Thickness 0.71mm Bulk density 0.132g/cm 3Oil absorption 8.0ml/g Water absorption 6.2ml/g Longitudinal dry tear length 801m Elongation 39% Lateral dry tear Cross-section length 680 m 〃 〃 Elongation 45% Longitudinal wet tear length 754 m 〃 〃 Elongation 43% Transverse wet tear length 572 m 〃 Elongation 48% Longitudinal redrying tear length 778 m 〃 〃 Elongation 50 % Transverse re-drying tearing length 649 m 〃 Elongation 61% This non-woven fabric does not change its physical and mechanical properties in the wet state or after re-drying from the wet state; It can be used in both dry and wet conditions and has potential use as a limited use or durable wiping cloth. Example A composite nonwoven fabric containing 74% fiberized pulp (Rayfluff It was made using the same method as in the example except that the wire roll nip gap was 30 1/4 inch and the wire roll nip gap was 105 mil. The measured characteristics are shown below. Basis weight 181g/m 2 Uncompressed thickness 4.06mm Bulk density 0.045g/cm 3 Oil absorption 26.8ml/g Longitudinal breaking length 59m 〃 Elongation 24% Lateral breaking length 139m 〃 Elongation 40% This nonwoven fabric is also soft and bulky. Compressible, like a cushion. It has characteristics such as somewhat resembling cotton wadding. Due to its high absorbency, it could be used in sanitary napkins, diapers, bandages, etc. Other uses include makeup removal pads, application pads, fillings, beauty pads (eg braziers), hairdressing and beauty aids, nursery products, and decorative uses. EXAMPLE A composite nonwoven fabric containing 50% hardwood pulp fibers and 50% melt-spun polypropylene microfibers was made according to the general process shown in FIG. Polypropylene resin (Exxon resin, CD—
523, containing 10% by weight of surfactant) at a final temperature of 635〓 and 0.33 per die orifice.
Extrude at a speed of 58 g/min, with a total polymer flow rate of 58 g/min.
Stretching was carried out in a primary air stream at a temperature of 690°C flowing at twice the mass flow rate. A secondary air stream containing floating pulp fibers is created by defibrating a roll pipe (hardwood with an average fiber length of 1.5 mm) in a Pitzka device without using a stripping air stream, and is made from the tip of the extrusion die by approx. At 2 inches, the primary air and polypropylene microfiber flow merged at right angles. The composite web was then deposited on the surface of a wire mesh covered vacuum roll 5.5 inches from the tip of the extrusion die. The various properties measured are shown below. Basis weight 85g/m 2 Thickness 1.57mm Bulk density 0.054g/cm 3 Moisture absorption 15.8ml/g Longitudinal dry tearing length 137m 〃 〃 Elongation 33% Horizontal dry tearing length 83m 〃 〃 Elongation 59% This web is easily wetted by water and has an extremely soft feel. The drapability is the same as the above-mentioned webs, but it has a softer surface texture. Example A composite nonwoven fabric containing 50% cedar pulp fibers and 50% melt-spun polypropylene microfibers was made using the same method as in the example. The secondary air flow containing pulp fibers has an average fiber length of 3.9mm.
It was made by defibrating roll pulp manufactured by Cedanier. The various properties measured are shown below. Basis weight 83g/m 2 Thickness 1.77mm Bulk density 0.047g/cm 3 Moisture absorption 18.9ml/g Longitudinal dry tearing length 119m 〃 〃 Elongation 26% Horizontal dry tearing length 60m 〃 〃 Elongation 46% This web is easily wetted by water. The equipment used in each of the above examples for ultrasonic calendering was the aforementioned Branson equipment set at 50 psi on the horn and at a web passage speed of 211 ft/min. Figures 6 to 8 are scanning electron micrographs of nonwoven fabrics produced by the following method. This nonwoven fabric is made of 50.4% soft wood pulp fibers (Longlac-18, pine pulp with an average fiber length of 3.2 mm) and 49.6% melt-spun polypropylene fibers (Exxon resin, CD-18).
It is a composite nonwoven fabric containing 392). The nonwoven fabric directs a secondary air stream carrying suspended wood pulp fibers at right angles to the primary air stream containing hot air and melt-spun polypropylene fibers to join approximately 2 inches from the die end. It was made by
Melt-spun fibers are made from polypropylene resin at a final temperature.
The spun fibers were extruded at a rate of 0.31 g/min per die orifice at a temperature of 630°, and the extruded spun yarn was drawn in a primary air flow at a temperature of 690° flowing at a mass flow rate of 66.1 times the total polymer flow rate. The secondary air flow is
It was made by feeding a carded web of wood pulp fibers through a pair of feed rolls into a fiber gun consisting of a pair of nozzles located on opposite sides of the web. That is, the carded web is unraveled into individual fibers by a high-speed air jet coming out of a nozzle, the fibers are introduced into a high-speed air stream, and this fiber stream is guided through a duct to join the primary air stream of the melt-spun fibers and then passed through an extrusion die. from the end
The composite web was deposited on the surface of a vacuum roll covered with wire mesh 5.5 inches apart. Figure 6 (80x) shows the uniformity of the composite fiber structure, the randomness of the fiber directions, the overall entanglement of the pulp fibers and the melt-spun fibers, and the relative diameters of both fibers. Figure 7 (300x magnification) further shows the overall entanglement of the melt-spun microfibers of the pulp fibers, the relative dimensions of the fibers, and the large voids within the web. Figure 8 (1000x magnification) shows a section of pulp fibers supported by a large number of intertwined microfibers. The diameter variation of melt spun fibers is typically 3-5 microns. There is not much bonding between polypropylene fibers within the web, but as you can see from the photo, there is bonding between large diameter fibers and fibers of different sizes (in the case of this photo, the fibers are approximately 14 microns in diameter). (fiber-to-fiber bonds of approximately 5 microns). This type of bonding is rare in bulky, low density webs, and it is clear that the primary basis for the web's shape retention is the extensive physical entanglement of both the pulp fibers and the melt-spun microfibers. No bond between polypropylene fibers and cellulose pulp fibers was found. This lack of interfiber bonding gives low density webs excellent softness, flexibility, and drapability. Because the surface and internal structure is uniform,
Nonwovens exhibit properties of both synthetic resin microfibers and pulp fibers. For example, even in composite nonwoven fabrics that are mostly pulp fibers, the presence of low surface energy microfibers on the surface limits their wettability. Additionally, the distribution of thermoplastic fibers throughout the web allows the web structure to be thermally modified through processes such as calendering, spot bonding, and lamination to other thermoplastic webs or films. Summer. Figures 9-11 are scanning electron micrographs of nonwoven fabrics made by the same method as described above, with the following exceptions. In other words, this nonwoven fabric has 48.5% soft wood pulp fiber (Longlac-18, average fiber length
3.2mm corn pine pulp) and 51.5% melt-spun polypropylene fiber (Exxon resin, CD-
392), extrusion speed per die orifice is 0.28g/min, primary air of 700〓 and 665
It was made with a mass flow ratio of 85:1 for the polymer 〓, and was further pressed against an anvil roll with an embossed pattern shown in Figures 3 and 4 and subjected to ultrasonic calendering to create a high-density material. It has become. Figure 9 (600x) and Figure 10 (600x) again
In this case, the web exhibits a general intertwining of melt-spun microfibers and pulp fibers in dense but non-embossed areas. FIG. 11 (300x magnification) shows an embossed portion corresponding to the recess 43 in FIG. 4, formed by intensive calendering. The fiber structure of the thermoplastic fibers is lost in this embossed area, and the resulting film serves to hold the pulp fibers firmly in place. Nonwoven fabrics typically calendered in this manner have increased tensile strength and density, and have decreased liquid absorption but increased liquid conductivity. Due to the presence of hydrophobic and water-resistant fibers, composite nonwoven fabrics are stable in water and water solvents. Additionally, polyolefin fibers increase the absorbency of oils and solvents. The incorporation of pulp fibers within the matrix of melt-spun microfibers results in increased bulk and a hollow structure. Due to the overall intertwining of pulp fibers and microfibers, the overall composite structure has good shape retention and abrasion resistance, and if necessary, an adhesive can be applied to stabilize the web structure. Although easy to use, this composite nonwoven fabric does not require adhesives. EXAMPLE Microfibers were produced by extruding polypropylene resin (Hercules PC 973) at the speeds and temperatures indicated for each series. The velocity of the primary air is 830 in all cases.
Although the speed was subsonic in the range of 1390ft/sec, the air temperature was kept constant at 665〓. The secondary air stream containing suspended pulp fluff is generated in the Pickker apparatus at an initial velocity of 77
ft/sec. It was made by defibrating a roll pipe (Rayfloc XJ. Southern pine pulp with an average fiber length of about 3.0 mm) using an air flow of about 14,401 bs/hr. The composite web was assembled onto a perforated vacuum roll 7.5 inches from the extrusion die tip. The properties of the composite nonwoven fabrics measured for Series A to Series E are summarized in Table 1, along with the data for Rayfloc XJ 100% pulp air-forming wadding.

【衚】【table】

【衚】【table】

【衚】 このデヌタは裂断長、氎分吞収性、および比容
積の回埩性に぀いお、―31も぀ず䜎い割合
でもの範囲におけるマむクロ繊維の広いスペク
トル効果を実蚌しおいる。䟋えば、朚材パルプ繊
維が100の繊維は、0.49psiの荷重を加えた埌の
回埩性の50以䞋であるが、皮類の繊維を含有
する䞍織垃は最䜎でも60以䞊の回埩性を瀺し、
ほずんどの詊料は80からそれ以䞊の高い回埩性
を瀺しおいる。 又、デヌタは、も぀ず䜎い割合でもの
マむクロ繊維含有量が耇合䞍織垃の氎分吞収性に
重芁な圱響をも぀こずを瀺しおいる。これは100
の朚材パルプ繊維を液䜓吞収胜力が芁求される
甚途おむ぀や女性甚ナプキンなどに䜿うには
非垞に郜合が良いこずを瀺す。安いコストで吞収
胜力を高めるこずができれば、競争の激しい垂堎
に優秀な性胜の補品を提䟛するこずが可胜になる
からである。 補品に高い圢状保持性が芁求される堎合には、
マむクロ繊維の含有量を40―60にしお甚いる
こずができる。この範囲では、たずえマむクロ繊
維ポリマヌが疎氎性であ぀おも十分高い吞収倀を
保持しおいるからである。 予想される通り、裂断長の倀はマむクロ繊維の
含有量を増加させるこずで簡単に増加する。しか
しながら、マむクロ繊維の含有量をないし
にたで䞋げるず裂断長に予想倖の商業的には重
芁なゞダンプが芋られる。これは朚材パルプ繊維
を99も含有するり゚ツブは高床の凊理技術なし
でも機械的に組立おたり、運んだり、加工するこ
ずができるこずを意味する。同様に、接着剀ある
いは他の特別な安定化技術を䜿甚しないで、すぐ
れた圢状保持性をも぀おむ぀甚の吞収芯を䜜るこ
ずが可胜である。 実斜䟋 XI 1.5ずのマむクロ繊維をそれぞれ含有す
る぀の詊料を、抌出し速床、ダむ枩床、空気枩
床を倚少䜎くしお、実斜䟋の詊料ず同じ方法で
䜜぀た。これら二぀の詊料に぀いお枬定した諞特
性を以䞋に瀺す。
[Table] This data demonstrates the broad spectrum effects of microfibers in the range of 7-31% (even lower percentages) on tear length, water absorption, and specific volume recovery. For example, a fiber made of 100% wood pulp fibers has less than 50% recovery after applying a load of 0.49 psi, whereas a nonwoven fabric containing two types of fibers has a recovery of at least 60% or more. ,
Most samples show high recovery rates of 80% and above. The data also show that a microfiber content of 7% (even a low percentage) has a significant effect on the moisture absorption of the composite nonwoven. This is 100
% wood pulp fibers are very suitable for use in applications where liquid absorption capacity is required (such as diapers and feminine napkins). This is because if absorption capacity can be increased at a lower cost, it will be possible to provide products with excellent performance in a highly competitive market. When products require high shape retention,
It can be used with a microfiber content of 40%-60%. This is because within this range, even if the microfiber polymer is hydrophobic, it maintains a sufficiently high absorption value. As expected, the breaking length value increases easily by increasing the microfiber content. However, the microfiber content should be between 3% and 1%.
%, there is an unexpected and commercially important jump in fracture length. This means that webs containing up to 99% wood pulp fiber can be mechanically assembled, transported and processed without sophisticated processing technology. Similarly, it is possible to make absorbent cores for diapers with excellent shape retention without the use of adhesives or other special stabilizing techniques. Example XI Two samples containing 1.5% and 3% microfibers, respectively, were made in the same manner as the sample in Example X, using slightly lower extrusion speeds, die temperatures, and air temperatures. The properties measured for these two samples are shown below.

【衚】【table】

【衚】 第図および第図に、䞊蚘実斜䟋およ
びXIで枬定した諞特性のいく぀かをグラフに瀺し
た。第図の氎平軞はマむクロ繊維の含有量を
衚わし、第図の氎平軞は朚材パルプ繊維の含
有量を衚わす。 第図の曲線は初期比容積を、曲線
は負荷時比容積を、曲線は回埩比容積
を衚わしおいる。回埩比容積はマむクロ繊維の含
有量が䜎レベルになるず急激に増加しおおりこ
の効果は第図にプロツトしなか぀たが実斜䟋
XIのデヌタによ぀おも明癜である、マむクロ繊
維がも぀ずも䜎いレベルのずきでさえも、最䜎25
c.c./は必らずあるこずがわかる。 第図には、実斜䟋の詊料の぀のシリヌ
ズ党郚に加えお、実斜䟋XIの二぀の詊料のデヌタ
がプロツトされおいる。しかし、プロツトしたデ
ヌタの間隙が比范的近いため、䞀本の曲線だけで
代衚させおある。プロツトしたデヌタの・印はシ
リヌズを、×印はシリヌズを、△印はシリヌ
ズを、□・印はシリヌズを、〓印はシリヌズ
を、△印は実斜䟋XIの぀の詊料を瀺す。第
図からわかるように、マむクロ繊維の含有量がも
぀ずも䜎い1.5ちようどにおいお吞収性が急激
に増加し、そしお吞収性はマむクロ繊維の含有量
が最䜎玄50に達するたでは100朚材パルプ䞍
織垃のレベル以䞊を維持しおいるこずがわかる。
マむクロ繊維の含有量が30以䞊においおは、吞
収性は、30から0.25×マむクロ繊維の重量パヌ
セントを匕いた差以䞊である。 第図には、実斜䟋のシリヌズの詊料の
リント数がプロツトされおいる。この曲線は耇合
䞍織垃の圢状保持性を衚わしおおり、圢状保持性
がほずんどないためふ぀うの方法では枬定するこ
ずさえできない100朚材パルプ䞍織垃の圢状保
持性が泚目に倀するほど改良されおいるこずがわ
かる。そのリント数は600から5.5×マむクロ繊
維の重量パヌセントを匕いた差以䞋である。 第図には、実斜䟋のシリヌズの詊料の
裂断長がプロツトされおいる。プロツトされたデ
ヌタの・印は瞊方向の裂断長を、×印は暪方向の
裂断長を瀺す。これらの曲線から、䞡方向の裂断
長はマむクロ繊維の含有量の増加ず共に挞次増加
しおいるこずがわかる。パルプ含有量が90以䞊
では、裂断長は必らず最䜎はあり、これは䞍
織垃がその自重で切れるずきの自由スパンが
であるこずを意味する。 参考実斜䟋 35.6の高捲瞮性ナむロンスフ玔床2.5デニ
ヌル、繊維長1.375むンチず64.6の溶融玡糞
ポリプロピレン繊維を含有する耇合䞍織垃で、浮
遊しおいるスフを搬送する次空気流を、高枩空
気ず溶融玡糞ポリプロピレン繊維を含む次空気
流に盎角に向けおダむ端郚から玄むンチの所で
合流させお䜜぀たものである。 溶融玡糞繊維はポリプロピレン暹脂を最終枩床
を630〓にしお、ダむオリフむス圓り0.25/min
の速床で抌し出しお生成し、党高分子流量の81倍
の質量流量で流れる枩床690〓の次空気流の䞭
で抌し出された玡糞を延䌞した。 次空気流は、察の䟛絊ロヌルを介しおナむ
ロンスフからなるカヌドり゚ツブをり゚ツブの反
察偎に配眮されたのノズルからなるフアむバヌ
ガンに送り蟌むこずによ぀お䜜぀た。すなわち、
ノズルから出る高速の空気ゞ゚ツトでカヌドり゚
ツプを個々の繊維に解きほぐしお繊維を高速気流
の䞭に投入し、この繊維流をダクトで導き、溶融
玡糞繊維の次空気流に合流させ、抌し出しダむ
端郚から5.5むンチ離れた金網でカバヌされた真
空ロヌルの衚面の䞊に耇合り゚ツブを集積させ
た。䞋蚘は枬定した特性である。 坪 量 56/m2 瞊方向の也燥裂断長 518 瞊方向の也燥䌞床 77 〃 の湿最裂断長 573 〃 〃 䌞床 87 瞊方向の也燥裂断長 330 〃 〃 䌞床 92 〃 の湿最裂断長 323 〃 〃 䌞床 78 このり゚ツブは匷じん性、匕匵匷さ、および䌞
床の改善の床合が倧きいこずに特城があり、䞊蚘
の諞実斜䟋の䞭で蚘茉したパルプずマむクロ繊維
の耇合䞍織垃にこれらの特性を付䞎する第䞉の成
分ずしおスフが䜿甚できるかも知れないこずを瀺
唆しおいる。スフ添加を含む成分又は成分䞍
織垃のいずれの堎合でも、その可胜性のある甚途
は衣服のむンタプヌシング、䞈倫な工業甚又は
家庭甚の拭垃、クリヌナ等を含たせたぬれ拭垃、
限定䜿甚の敷きマツトやテヌブルクロス、および
これに類する䞍織垃の利甚などの分野になろう。
[Table] Figures 14 and 15 show graphs of some of the properties measured in the above Examples and XI. The horizontal axis in Figure 14 represents the microfiber content, and the horizontal axis in Figure 15 represents the wood pulp fiber content. Curve 100 in FIG. 12 represents the initial specific volume; curve 1
01 represents the specific volume under load, and the curve 102 represents the recovery specific volume. The recovery specific volume increased rapidly at low levels of microfiber content (this effect was not plotted in Figure 12, but was shown in the example).
XI data), even at very low levels of microfibers, at least 25
You can see that cc/g is always present. Figure 13 plots data for all five series of Example samples, plus two samples of Example XI. However, since the gaps in the plotted data are relatively close, only one curve is used to represent it. In the plotted data, the * mark indicates series A, the × mark indicates series B, the △ mark indicates series C, the □ mark indicates series D, and the 〓 mark indicates series E.
, △ indicates two samples of Example XI. 13th
As can be seen from the figure, the absorbency increases rapidly at the lowest microfiber content, around 1.5%, and the absorbency decreases from 100% to 100% wood pulp until the microfiber content reaches a minimum of about 50%. It can be seen that the level of non-woven fabric is maintained.
At microfiber contents of 30% and above, the absorbency is greater than or equal to 30 minus 0.25 times the weight percentage of microfibers. This curve represents the shape retention of the composite nonwoven fabric, and it is noteworthy that the shape retention of the 100% wood pulp nonwoven fabric, which has almost no shape retention and cannot even be measured using normal methods. It can be seen that the lint count is less than 600 minus 5.5 x (weight percent of microfibers). Figure 15 shows a plot of the tear length for the Example Series A samples. In the plotted data, the * mark indicates the tearing length in the longitudinal direction, and the × mark indicates the tearing length in the transverse direction.From these curves, it can be seen that the tearing length in both directions corresponds to an increase in the microfiber content. It can be seen that when the pulp content is 90% or more, the breaking length is always at least 5 m, which means that the free span when the nonwoven fabric breaks under its own weight is 5 m.
It means that. Reference Example: A composite nonwoven fabric containing 35.6% high crimp nylon sulphate (purity 2.5 denier, fiber length 1.375 inches) and 64.6% melt-spun polypropylene fiber, the secondary air flow carrying the suspended sulphur was The primary air stream containing hot air and melt-spun polypropylene fibers was oriented perpendicularly to meet approximately 2 inches from the end of the die. The melt-spun fiber is made of polypropylene resin at a final temperature of 630〓 and 0.25 g/min per die orifice.
The extruded spun yarn was drawn in a primary air flow at a temperature of 690°C flowing at a mass flow rate of 81 times the total polymer flow rate. The secondary air flow was created by feeding a carded web of nylon fiber through a pair of supply rolls into a fiber gun consisting of a nozzle located on opposite sides of the web. That is,
A high-velocity air jet from the nozzle unravels the carded web into individual fibers, which feed the fibers into a high-velocity air stream that is guided through a duct to join the primary air stream of the melt-spun fibers and pass through the end of the extrusion die. The composite web was deposited on the surface of a vacuum roll covered with wire mesh 5.5 inches from the surface. The following are the measured characteristics. Basis weight 56g/m 2Longitudinal dry tearing length 518m Longitudinal dry elongation 77% Wet tearing length 573m Elongation 87% Longitudinal dry tearing length 330m Elongation 92% Wet breaking length: 323 m Elongation: 78% This web is characterized by a large degree of improvement in toughness, tensile strength, and elongation, and is superior to the pulps described in the examples above. This suggests that fabric may be used as a third component to impart these properties to microfiber composite nonwovens. In the case of either two-component or three-component nonwovens containing sulphate additives, their possible uses include garment interfacing, durable industrial or household wipes, wet wipes impregnated with cleaners, etc.
This will likely include the use of limited-use mats, tablecloths, and similar non-woven fabrics.

【図面の簡単な説明】[Brief explanation of the drawing]

第図は本発明にかかる䞍織垃に補造方法ず補
造装眮を瀺す郚分断面、郚分略偎面図。第図は
䞍織垃の郚分斜芖図。第図ぱンボス加工した
䞍織垃の郚分斜芖図。第図は第図の䞍織垃を
線―で切断した郚分断面図。第図は異぀た
゚ンボス暡様を䜿甚した䞍織垃の郚分斜芖図。第
図〜第図は兞型的な実斜䟋50の軟質朚材
パルプ繊維ず50ポリプロピレンマむクロ繊維か
らなる耇合䞍織垃をいろいろな倍率で撮圱した
走査電子顕埮鏡写真である。第図は80倍、第
図は300倍、第図は1000倍である。第図〜第
図は第の兞型的な実斜䟋48.5の軟質朚
材繊維ず51.5のポリプロピレン・マむクロ繊維
からなる耇合䞍織垃の走査電子顕埮鏡写真であ
る。第図600倍ず第図600倍は非゚
ンボス郚分を、第図300倍ぱンボス郚
分をそれぞれ瀺す。第図〜第図は本発明
に蚘茉した諞実斜䟋のいく぀かに぀いお枬定した
デヌタをわかり易くグラフに瀺したものである。  次空気流、 ノズルヘツド、
 ノズル、 次空気流、 耇
合流、 ピツカ・ロヌル、 ロヌルパル
プ、 送りロヌル、 ダクト、 ハ
りゞング、 通路、 ダクト、
 真空ロヌル、 真空ノズル、
 耇合り゚ツブ、 巻取りロヌル、 超
音波カレンダ加工ヘツド、 アンビルロヌ
ル、 超音波装眮、′ 非゚ンボス郚
分、 ゚ンボス郚分、 ゚ンボス郚分。
FIG. 1 is a partially sectional and partially schematic side view showing a method and apparatus for producing a nonwoven fabric according to the present invention. FIG. 2 is a partial perspective view of the nonwoven fabric. FIG. 3 is a partial perspective view of an embossed nonwoven fabric. FIG. 4 is a partial cross-sectional view of the nonwoven fabric shown in FIG. 3 taken along line 4--4. FIG. 5 is a partial perspective view of a nonwoven fabric using different embossed patterns. Figures 6-8 are scanning electron micrographs taken at various magnifications of a typical example (composite nonwoven fabric consisting of 50% soft wood pulp fibers and 50% polypropylene microfibers). Figure 6 is 80x, Figure 7
The figure is 300x, and Figure 8 is 1000x. Figures 9-11 are scanning electron micrographs of a second exemplary embodiment (composite nonwoven fabric consisting of 48.5% soft wood fibers and 51.5% polypropylene microfibers). Figures 9 (600x) and 10 (600x) show the non-embossed part, and Figure 11 (300x) shows the embossed part. FIGS. 12 to 15 are graphical representations of data measured for some of the embodiments described in the present invention for easy understanding. 10...Primary air flow, 11...Nozzle head, 1
2, 13... Nozzle, 14... Secondary air flow, 15... Combined flow, 20... Picker roll, 21... Roll pulp, 22... Feed roll, 23... Duct, 24... Housing, 25... Passage, 26... Duct, 30,3
1... Vacuum roll, 32, 33... Vacuum nozzle, 34
...Composite web, 35... Winding roll, 40... Ultrasonic calendering head, 41... Anvil roll, 42... Ultrasonic device, 35'... Non-embossed portion, 43... Embossed portion, 44... Embossed portion.

Claims (1)

【特蚱請求の範囲】  熱可塑性高分子を溶融玡糞しお埗られる平均
盎埄10ミクロン以䞋のマむクロ繊維から圢成され
た母䜓ず、該母䜓内に拘束された状態ずなるよう
に、前蚘母䜓の党䜓にわた぀お分散され、前蚘マ
むクロ繊維に察しお機械的に絡み合うこずによ぀
お連結された朚材パルプ繊維ずから構成された䞍
織垃であ぀お、 前蚘マむクロ繊維ず、解繊された状態の前蚘朚
材パルプ繊維ずが、空気䞭でじよう乱状態の䞋で
混合されお、前蚘朚材パルプ繊維が前蚘マむクロ
繊維の少なくずも䞀郚に係合し、前蚘マむクロ繊
維が盞互に離間した構造の耇合繊維組織が圢成さ
れおおり、前蚘マむクロ繊維ず前蚘朚材パルプ繊
維ずは、いかなる接着、分子結合、あるいは氎玠
結合もなく、緊密な結合状態ずな぀おいるこずを
特城ずする䞍織垃。  前蚘マむクロ繊維が高枩の柔らかい生成初期
の状態にあるずきに、該マむクロ繊維ず前蚘朚材
パルプ繊維ずが、空気䞭でじよう乱状態䞋に混合
されたものである特蚱請求の範囲第項蚘茉の䞍
織垃。  前蚘朚材パルプ繊維が前蚘マむクロ繊維の母
䜓党䜓に䞀様に分垃しお均質な䞍織垃を圢成しお
いる特蚱請求の範囲第項蚘茉の䞍織垃。  前蚘朚材パルプ繊維の長さが玄0.5〜10mmの
範囲内にあり、その長さず最倧暪幅ずの比が玄
10〜400の範囲内にある特蚱請求の範囲
第項蚘茉の䞍織垃。  前蚘マむクロ繊維の平均盎埄が玄ミクロン
以䞊である特蚱請求の範囲第項蚘茉の䞍織垃。  前蚘マむクロ繊維が䞍織垃の重量の玄〜
80を占める特蚱請求の範囲第項蚘茉の䞍織
垃。  前蚘䞍織垃の回埩比容積が少くずも初期比容
積の75である特蚱請求の範囲第項蚘茉の䞍織
垃。  前蚘マむクロ繊維が䞍織垃の重量の玄25以
䞋である特蚱請求の範囲第項蚘茉の䞍織垃。  前蚘マむクロ繊維が少くずも䞍織垃の重量の
を占め、リント数が600から5.5×マむクロ
繊維の重量癟分率を匕いた差以䞋である特蚱請
求の範囲第項蚘茉の䞍織垃。  前蚘朚材パルプ繊維が少くずも䞍織垃の重
量の40を占め、回埩容積が少くずも25である特
蚱請求の範囲第項蚘茉の䞍織垃。  前蚘マむクロ繊維が少くずも䞍織垃の重量
の玄30を占め、吞収性が30から0.25×マむク
ロ繊維の重量癟分率を枛じた差より倧きい特蚱
請求の範囲第項蚘茉の䞍織垃。  前蚘朚材パルプ繊維が少くずも䞍織垃の重
量の玄90を占め、裂断長が少くずもである
特蚱請求の範囲第項蚘茉の䞍織垃。  前蚘䞍織垃の初期比容積が少くずも25であ
り、回埩比容積が初期比容積の少くずも75であ
り、リント数が600から5.5×マむクロ繊維の重
量癟分率を枛じた差より小さく、吞収性が30か
ら0.25×マむクロ繊維の重量癟分率ず枛じた
差より倧きく、裂断長が少くずもはある特蚱
請求の範囲第項蚘茉の䞍織垃。  匕長匷さ、吞収性、および颚合に぀いお独
特な組合せ特性を有する䞍織垃の補造方法におい
お、 (a) 䞀般に䞍連続な熱可塑性高分子マむクロ繊維
からなる溶融玡糞マむクロ繊維を含み、枩床が
箄600〓〜700〓の範囲にある次空気流を䜜
り、 (b) 解繊した朚材パルプ繊維を含む次空気流を
䜜り、 (c) 前蚘次空気流に前蚘次空気流をじよう乱
状態のもずで合流させ、前蚘マむクロ繊維ず前
蚘朚材パルプ繊維ずの完党な混合物を含む耇合
空気流を䜜り、 (d) 前蚘耇合空気流をり゚ツブ圢成面に導き、そ
の䞊に前蚘マむクロ繊維から成る母䜓を空気成
圢し、このずき、該母䜓内でマむクロ繊維の䞀
郚が少くずも解繊された朚材パルプ繊維によ぀
お盞互に䞀定間隔を眮いお離れるように結合さ
れ、たた、前蚘解繊された朚材パルプ繊維は前
蚘マむクロ繊維の母䜓党䜓にわた぀お分散し、
マむクロ繊維ず機械的に絡み合うこずによ぀お
盞互連結され䞔぀前蚘母䜓内に拘束され、いか
なる接着、分子結合あるいは氎玠結合もなく、
䞡繊維の機械的な絡み合いのみで緊密な結合の
耇合繊維組織を圢成するこずから成る方法。  真盎な少くずも列の耇数の抌し出し孔か
ら抌し出した高分子フむラメントを延䌞するこず
によ぀お前蚘マむクロ繊維を生成する特蚱請求の
範囲第項蚘茉の補造方法。  前蚘マむクロ繊維が高枩の柔らかい生成初
期の状態にあるずきに、前蚘次空気流ず次空
気流ずを合流させる特蚱請求の範囲第項蚘茉
の補造方法。  前蚘朚材パルプ繊維を前蚘マむクロ繊維の
母䜓党䜓にわた぀お䞀様に分垃させお均質な䞍織
垃を圢成する特蚱請求の範囲第項蚘茉の補造
方法。  前蚘朚材パルプ繊維の長さを玄0.5〜10mm
の範囲にし、その長さず最倧暪幅ずの比を玄10
〜400の範囲にする特蚱請求の範囲第
項蚘茉の補造方法。  前蚘マむクロ繊維の平均盎埄を玄ミクロ
ン以䞊にする特蚱請求の範囲第項蚘茉の補造
方法。  前蚘マむクロ繊維が繊維混合物の重量の玄
〜80を占めるようにする特蚱請求の範囲第
項蚘茉の補造方法。  前蚘マむクロ繊維を前蚘繊維混合物の重量
の玄25以䞋にする特蚱請求の範囲第項蚘茉
の補造方法。
[Scope of Claims] 1. A base body formed from microfibers with an average diameter of 10 microns or less obtained by melt-spinning a thermoplastic polymer, and a matrix formed from microfibers having an average diameter of 10 microns or less, and the entire base body so as to be restrained within the base body. A nonwoven fabric comprising wood pulp fibers dispersed throughout the microfibers and connected to the microfibers by mechanically entangling them, the microfibers and the wood pulp in a defibrated state. and the fibers are mixed in air under turbulent conditions to form a composite fiber structure in which the wood pulp fibers engage at least a portion of the microfibers and the microfibers are spaced apart from each other. A nonwoven fabric characterized in that the microfibers and the wood pulp fibers are tightly bonded without any adhesion, molecular bonding, or hydrogen bonding. 2. Claim 1, wherein the microfibers and the wood pulp fibers are mixed in the air under a turbulent condition when the microfibers are in a soft initial state of production at a high temperature. Nonwoven fabric as described. 3. The nonwoven fabric according to claim 1, wherein the wood pulp fibers are uniformly distributed throughout the matrix of microfibers to form a homogeneous nonwoven fabric. 4 The length of the wood pulp fiber is within the range of about 0.5 to 10 mm, and the ratio of the length to the maximum width is about
The nonwoven fabric according to claim 1, which has a molecular weight within the range of 10/1 to 400/1. 5. The nonwoven fabric of claim 1, wherein the microfibers have an average diameter of about 1 micron or more. 6 The microfibers account for about 1% or more of the weight of the nonwoven fabric.
The nonwoven fabric according to claim 1, which accounts for 80%. 7. The nonwoven fabric according to claim 1, wherein the recovery specific volume of the nonwoven fabric is at least 75% of the initial specific volume. 8. The nonwoven fabric of claim 1, wherein the microfibers constitute about 25% or less of the weight of the nonwoven fabric. 9. The nonwoven fabric of claim 1, wherein the microfibers account for at least 5% of the weight of the nonwoven fabric, and the lint count is less than or equal to 600 minus 5.5 x (weight percentage of microfibers). 10. The nonwoven fabric of claim 1, wherein the wood pulp fibers account for at least 40% of the weight of the nonwoven fabric and have a recovery volume of at least 25%. 11. The nonwoven fabric of claim 1, wherein the microfibers account for at least about 30% of the weight of the nonwoven fabric, and the absorbency is greater than 30 minus 0.25 x (weight percentage of microfibers). 12. The nonwoven fabric of claim 1, wherein the wood pulp fibers account for at least about 90% of the weight of the nonwoven fabric and have a tear length of at least 5 meters. 13. the nonwoven fabric has an initial specific volume of at least 25, a recovery specific volume of at least 75% of the initial specific volume, and a lint number less than 600 minus 5.5 x (weight percentage of microfibers); Nonwoven fabric according to claim 1, having an absorbency greater than 30 minus 0.25 x (weight percentage of microfibers) and a tearing length of at least 5 m. 14. A method of manufacturing a nonwoven fabric having a unique combination of properties of tensile strength, absorbency, and hand, comprising: (b) creating a secondary air flow containing defibrated wood pulp fibers; (c) adding said secondary air flow to said primary air flow; merging under turbulent conditions to create a composite air stream containing an intimate mixture of said microfibers and said wood pulp fibers; (d) directing said composite air stream to a web-forming surface over which said microfibers are formed; A matrix of fibers is air-formed, at which time some of the microfibers are bonded to each other at regular intervals by at least defibrated wood pulp fibers, and The defibrated wood pulp fibers are dispersed throughout the microfiber matrix;
interconnected by mechanical intertwining with the microfibers and confined within the matrix, without any adhesion, molecular or hydrogen bonding;
A method consisting of forming a tightly bonded composite fiber structure only by mechanically intertwining both fibers. 15. The manufacturing method according to claim 14, wherein the microfibers are produced by drawing a polymer filament extruded from at least one row of straight extrusion holes. 16. The manufacturing method according to claim 14, wherein the primary air flow and the secondary air flow are combined when the microfibers are in a high temperature and soft initial state of production. 17. The manufacturing method according to claim 14, wherein the wood pulp fibers are uniformly distributed throughout the matrix of microfibers to form a homogeneous nonwoven fabric. 18 The length of the wood pulp fibers is approximately 0.5 to 10 mm.
range, and the ratio of the length to the maximum width is approximately 10/
Claim 14 in the range of 1 to 400/1
Manufacturing method described in section. 19. The method of claim 14, wherein the microfibers have an average diameter of about 1 micron or more. 20. Claim 1, wherein the microfibers account for about 1 to 80% of the weight of the fiber mixture.
The manufacturing method described in Section 4. 21. The method of claim 14, wherein the microfibers are less than about 25% by weight of the fiber mixture.
JP12564577A 1977-10-18 1977-10-18 Nowoven fabric and production thereof Granted JPS5459466A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12564577A JPS5459466A (en) 1977-10-18 1977-10-18 Nowoven fabric and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12564577A JPS5459466A (en) 1977-10-18 1977-10-18 Nowoven fabric and production thereof

Publications (2)

Publication Number Publication Date
JPS5459466A JPS5459466A (en) 1979-05-14
JPS6260492B2 true JPS6260492B2 (en) 1987-12-16

Family

ID=14915141

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12564577A Granted JPS5459466A (en) 1977-10-18 1977-10-18 Nowoven fabric and production thereof

Country Status (1)

Country Link
JP (1) JPS5459466A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03126784U (en) * 1990-04-04 1991-12-20

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57121657A (en) * 1981-01-22 1982-07-29 Mitsui Petrochemical Ind Absorbing material
US4468428A (en) * 1982-06-01 1984-08-28 The Procter & Gamble Company Hydrophilic microfibrous absorbent webs
DK167952B1 (en) * 1983-03-10 1994-01-10 Procter & Gamble ABSORBENT STRUCTURE, WHICH IS A MIXTURE OF HYDROFILE FIBERS AND WATER-SOLUBLE HYDROGEL IN THE FORM OF SEPARATE PARTICLES OF CROSS-BOND POLUMED MATERIAL, PROCEDURE FOR THE PREPARATION OF SAME AND SINGLE PREPARATION
BR8501093A (en) * 1985-03-12 1986-10-21 Johnson & Johnson S P A FIBER VEHICLE FORMING EQUIPMENT
IT1219196B (en) * 1988-04-11 1990-05-03 Faricerca Spa FIBROUS COMPOSITION FOR ABSORBENT MATTRESSES METHOD OF MANUFACTURE OF AN ABSORBENT MATERIAL STARTING FROM SUCH COMPOSITION AND ABSORBENT MATERIAL PRODUCED BY SUCH METHOD

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03126784U (en) * 1990-04-04 1991-12-20

Also Published As

Publication number Publication date
JPS5459466A (en) 1979-05-14

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