JPH03287847A - Fiber ball for wadding - Google Patents
Fiber ball for waddingInfo
- Publication number
- JPH03287847A JPH03287847A JP8195690A JP8195690A JPH03287847A JP H03287847 A JPH03287847 A JP H03287847A JP 8195690 A JP8195690 A JP 8195690A JP 8195690 A JP8195690 A JP 8195690A JP H03287847 A JPH03287847 A JP H03287847A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- fibers
- binder
- fineness
- melting point
- 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.)
- Granted
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 126
- 239000011230 binding agent Substances 0.000 claims abstract description 31
- 238000002844 melting Methods 0.000 claims abstract description 15
- 230000008018 melting Effects 0.000 claims abstract description 14
- 229920000728 polyester Polymers 0.000 claims abstract description 11
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 claims abstract 2
- 238000011049 filling Methods 0.000 claims description 6
- 238000011084 recovery Methods 0.000 abstract description 11
- 239000007789 gas Substances 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 3
- 239000012209 synthetic fiber Substances 0.000 abstract description 3
- 229920002994 synthetic fiber Polymers 0.000 abstract description 3
- 230000000266 injurious effect Effects 0.000 abstract 1
- 230000006835 compression Effects 0.000 description 12
- 238000007906 compression Methods 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000000945 filler Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- -1 polypropylene Polymers 0.000 description 5
- 238000002788 crimping Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 239000000779 smoke Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000009415 formwork Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 101000802478 Sylvirana guentheri Brevinin-2GHa Proteins 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000011176 biofiber Substances 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000003562 lightweight material Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Nonwoven Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は家具用、ベツド、クツション等に用いられる繊
維、充填材料に関し、特に発泡ポリウレタン代替用とし
て製造時にフロン等を用いず、また、燃焼時に有害ガス
を発生せず2弾性回復性。Detailed Description of the Invention (Industrial Field of Application) The present invention relates to fibers and filler materials used for furniture, beds, cushions, etc., and in particular, as a substitute for foamed polyurethane, it does not use fluorocarbons or the like during production, and is combustible. 2. Elastic recovery without emitting harmful gases.
耐ヘタリ性が優れている繊維充填材料に関するものであ
る。This invention relates to a fiber-filled material that has excellent resistance to settling.
(従来の技術)
従来、椅子の内張り、マツトレス、ベツド等の充填材と
して発泡ウレタンが多く用いられてきた。(Prior Art) Foamed urethane has conventionally been widely used as a filler for chair linings, pinerests, beds, and the like.
発泡ポリウレタンは立体的な網目構造を有しており、軽
量で圧縮回復性、耐ヘタリ性の優れた材料であるが、製
造時に地球のオゾン層を破壊するフロンガスを使用する
こと及び燃焼時に発煙が多く。Foamed polyurethane has a three-dimensional network structure, and is a lightweight material with excellent compression recovery and fatigue resistance. A lot.
有害ガス発生の懸念かあり、火事になった除煙に巻かれ
る等の大きな問題点が指摘されている。There are concerns about the generation of harmful gases, and major problems have been pointed out, such as people getting caught in smoke removers that catch fire.
一方9合成短繊維で比較的太繊度(5デニ一ル以上)の
ものを梳綿し積層後、接着剤や低融点バインダー繊維を
用いて成型し、家具クベノド、枕等のクツション材とし
て用いられているが、この製造方法では繊維の方向は横
方向や縦方向に配列することはできるが、成型体の高さ
方向には配列させることができないため、上下方向から
加わる力に対しては回復性が乏しくなるというような欠
点を有するのである。On the other hand, 9 synthetic staple fibers with relatively thick fineness (5 denier or more) are carded and laminated, then molded using adhesive or low-melting binder fibers and used as cushioning materials for furniture, pillows, etc. However, with this manufacturing method, the fibers can be arranged in the horizontal and vertical directions, but cannot be arranged in the height direction of the molded product, so it is difficult to recover from forces applied from above and below. However, it has the disadvantage of poor performance.
(発明が解決しようとする問題点)
上述のように、従来用いられてきた家具用充填材として
は環境破壊ヤ燃焼時の発煙が少なく、シかも圧縮回復性
や耐ヘタリ性が良好であるものはなかった。(Problems to be Solved by the Invention) As mentioned above, conventionally used furniture fillers cause less environmental damage and smoke when burned, and have good compression recovery properties and resistance to set. There was no.
本発明者らは環境破壊や燃焼時の発煙が少なくまた有害
ガスの発生もなく、シかも圧縮回復性や耐ヘタリ性が発
泡ポリウレタンに劣らない性能を有するものを得んとし
て種々検討の結果2合成短繊維が三次元的に絡み合う構
造を形成し、しかも繊維相互を適度に接着することによ
り、圧縮回復性が優れ、耐ヘタリ性の少ない繊維充填物
を見い出したものである。The inventors of the present invention have conducted various studies in an effort to create a product that causes less environmental damage and smoke during combustion, does not generate harmful gases, and has compression recovery and fatigue resistance comparable to that of polyurethane foam.2 By forming a structure in which short synthetic fibers are intertwined three-dimensionally and by appropriately adhering the fibers to each other, a fiber filler has been discovered that has excellent compression recovery properties and low resistance to set.
(課題を解決するための手段)
即ち2本発明は繊度3〜30デニール、長さ10〜70
mの実質的に捲縮を有しない合成短繊維(A)と。(Means for solving the problems) That is, the present invention has a fineness of 3 to 30 denier and a length of 10 to 70 denier.
m of synthetic short fibers (A) having substantially no crimps.
繊度3〜100デニール、長さ10〜100襲の実質的
に捲縮を有せず、しかも前記合成短繊維(A)と相溶性
を有し、該合成短繊維(A)の融点より20°C以上低
い粘着温度を有するバインダー繊維(B)が重量比で9
0〜50%/10〜50%の割合でブレンドされた平均
径5〜50mである詰綿用ファイバーボールである。It has a fineness of 3 to 100 deniers, a length of 10 to 100 denier, substantially no crimp, and is compatible with the synthetic short fiber (A), and is 20° below the melting point of the synthetic short fiber (A). The binder fiber (B) having a lower adhesion temperature than C is 9 in weight ratio.
This is a fiber ball for filling having an average diameter of 5 to 50 m, blended at a ratio of 0 to 50%/10 to 50%.
本発明において合成短繊維(A)とは、ポリエステル、
ポリビニルアルコール、ポリプロピレン等がその対象と
なるが、剛性の高いポリエステル等が圧縮回復性や耐ヘ
タリ性の面から最も好ましい。In the present invention, synthetic staple fibers (A) include polyester,
Polyvinyl alcohol, polypropylene, and the like are suitable, but highly rigid polyester and the like are most preferable from the viewpoint of compression recovery properties and fatigue resistance.
また、上記特性を損わない範囲で共重合、フレンド等に
より改質した繊維を使用できる。また、これらの合成短
繊維中に従来公知の着色剤、制電剤。Furthermore, fibers modified by copolymerization, friends, etc. can be used within a range that does not impair the above characteristics. In addition, conventionally known coloring agents and antistatic agents are contained in these synthetic staple fibers.
難燃剤、艶消剤等を練り込むことも可能である。It is also possible to incorporate flame retardants, matting agents, etc.
バインダー繊維(B)としては、ポリプロピレン。The binder fiber (B) is polypropylene.
ポリエチレン、低融点ポリエステルの単一型や低融点成
分を鞘部に配した芯鞘型懺維を用いろことができる。It is possible to use a single type of polyethylene or low melting point polyester, or a core/sheath type fiber in which a low melting point component is arranged in the sheath part.
また、バインダー繊維(B)の粘着温度は合成短繊維(
A)の融点より20°C以上低くなければならない。粘
着温度が合成短繊維(A)の融点との差が20°C未満
となると熱処理時に合成短繊維(A)が変形したり、ひ
どい場合には溶融するため圧縮回復性が乏しくなり、ま
た非常に硬くなるという欠点を有する。In addition, the adhesion temperature of the binder fiber (B) is the synthetic staple fiber (
It must be at least 20°C lower than the melting point of A). If the difference between the adhesion temperature and the melting point of the synthetic short fiber (A) is less than 20°C, the synthetic short fiber (A) will be deformed during heat treatment, or in severe cases will melt, resulting in poor compression recovery properties and extremely It has the disadvantage of being hard.
次に、バインダー繊維(B)は合成短繊維(A)と相溶
性を有する必要がある。相溶性がないと熱処理しても接
着性が乏しいため得られた成型体の強度がなく、外力で
その構造が破壊されるため充填材としての機能を有しな
くなるのである。合成短繊維(A)とバインダー繊維C
B)との組合せとしては、ポリエチレン−ポリプロピレ
ン、ポリエステル−低融点ポリエステル等があるが、圧
縮回復性。Next, the binder fiber (B) needs to be compatible with the synthetic staple fiber (A). If there is no compatibility, the resulting molded product will lack strength due to poor adhesion even after heat treatment, and its structure will be destroyed by external force, so it will no longer function as a filler. Synthetic short fibers (A) and binder fibers C
Combinations with B) include polyethylene-polypropylene, polyester-low melting point polyester, etc., which have good compression recovery properties.
耐ヘタリ性が良好なポリエステル−低融点ポリエステル
が最も好ましい。Most preferred is a polyester-low melting point polyester that has good resistance to settling.
合成短繊維中枕バインダー繊維の捲縮につ(・では、フ
ァイバーボールの作り易さの点で実質的に有しないこと
が必要である。捲縮を有した繊維を用いると捲縮のため
繊維相互の分散が不良になり。Synthetic staple fibers In the case of crimping of the binder fibers, it is necessary that the binder fibers have virtually no crimping in order to facilitate the production of fiber balls.If crimped fibers are used, the fibers Mutual dispersion becomes poor.
球状に集合することが不可能となる。It becomes impossible to aggregate into a spherical shape.
次に9合成短繊維及びバインダー繊維の繊度であるが、
3〜30デニールの範囲になければならない。繊度が3
デニ一ル未満であると、繊維の腰が不充分になり、成型
した後ベツド等に充填しても底つき感が出て好ましくな
い。また、繊度が30デニールを越えると繊維の剛性が
犬となり、柔軟性に乏しくなり好ましくない。Next, the fineness of 9 synthetic short fibers and binder fibers is as follows.
Must be in the range of 3-30 denier. Fineness is 3
If the denier is less than 1, the stiffness of the fibers will be insufficient, and even if it is filled into a bed or the like after being molded, it will give a feeling of bottoming out, which is not preferable. Furthermore, if the fineness exceeds 30 denier, the stiffness of the fibers will be too high, resulting in poor flexibility, which is not preferable.
また9合成短繊維及びバインダー繊維の繊維長、は繊度
と関係し、細繊度繊維はど短(、太繊度繊維は相対的に
長くなるが、上記の繊度範囲では10〜70龍にする必
要がある。loim未満であると後述するよう(τファ
イバーボールの径が5正未満になり、70龍を越えろと
繊維相互の絡み合いが激しくなり、ファイバーボールに
することが著しく困難となる。In addition, the fiber length of 9 synthetic staple fibers and binder fibers is related to the fineness, with fine-grained fibers being relatively short (and thick-fibers being relatively long, but in the above fineness range, it is necessary to make them 10 to 70 long). As will be described later, if the diameter is less than loim (τ), the diameter of the fiber ball will be less than 5 mm, and if it exceeds 70 mm, the intertwining of the fibers will become severe, making it extremely difficult to form a fiber ball.
なお9合成短繊維及びバインダー繊維の繊度及び繊維長
は両者共同じ程度にすることが好ましい。Note that it is preferable that the fineness and fiber length of the synthetic short fibers and the binder fibers are the same.
こnはファイバーボールを作る際1両繊維のブレンドが
均一になると共にファイバーボール化がし易くなるため
である。This is because when making a fiber ball, the blend of both fibers becomes uniform and it becomes easier to form a fiber ball.
次に9合成短繊維とバインダー繊維の混率であるが、9
0〜50wt%/ 10〜50wt%の範囲にしなけれ
ばならない。合成短繊維が90wt%を越えると相補的
にバインダー繊維の量が10wt%未満となり。Next is the blend ratio of 9 synthetic staple fibers and binder fibers.
Must be in the range of 0-50wt%/10-50wt%. When the synthetic staple fiber exceeds 90 wt%, the complementary amount of binder fiber becomes less than 10 wt%.
ファイバーボールを熱処理により成型してもファイバー
ボールの繊維接着点が少なくなり、外力に対してファイ
バーボールの立体形状を維持することが困難であり、圧
縮回復性及び耐ヘタリ性が著しく悪化する。また2合繊
短繊維が50%未満になると相補的にバインダー繊維量
が50チを越えるため、熱処理して成型したファイバー
ボールが硬(なり、ベツド等に充填した場合不快な凹凸
感がでて好ましくない。Even if the fiber ball is molded by heat treatment, the number of fiber adhesion points in the fiber ball decreases, making it difficult to maintain the three-dimensional shape of the fiber ball against external forces, and the compression recovery property and set resistance are significantly deteriorated. In addition, if the amount of the two-synthetic short fibers is less than 50%, the amount of complementary binder fibers exceeds 50, which is not preferable because the heat-treated and molded fiber balls become hard (and create an unpleasant uneven feel when filled in a bed etc.). do not have.
次vc、7丁イバーボールの形状であるカッヘッド等に
充填した場合上下、左右からの外力に対して抵抗力を有
するよう真球状が好ましいが、充填する家具等の形状か
ら扁平球状であってもさしつかえない。When filling a cuphead etc. in the shape of a 7-bar ball, it is preferable to have a true spherical shape so as to have resistance against external forces from the top, bottom, left and right, but due to the shape of the furniture etc. to be filled, a flat spherical shape is also acceptable. I can't help it.
ファイバーボールの径としては5〜50m程度が必要で
ある。5龍未満であると使用するファイバー・ボールの
量が多くなるため高価になると共に軽量化が困難となる
。また、径が50目を越えると充填した場合にファイバ
ーボールとファイノ(−ボールの間に大きな空隙ができ
るため、凹凸感が出てくるため好ましくない。The fiber ball needs to have a diameter of about 5 to 50 m. If it is less than 5 dragons, the amount of fiber balls used will increase, making it expensive and difficult to reduce weight. Moreover, if the diameter exceeds 50, a large gap will be formed between the fiber balls and the phyno balls when filled, resulting in an uneven feeling, which is not preferable.
ファイバーボールの製造方法としては、上記したような
特定の繊度、繊維長を有する合成短繊維とバインダー繊
維とを特定の比率で水を満たした水槽に分散させ、空気
を連続的に吸い込むか、攪拌機で1〜10時間攪拌する
ことにより繊維群が分散ヤ集合を繰り返し、均一なファ
イノ(−ボールを形成させるのである。Fiber balls can be produced by dispersing synthetic short fibers with a specific fineness and fiber length as described above and binder fibers in a specific ratio in a water tank filled with water, and then continuously sucking in air or using a stirrer. By stirring for 1 to 10 hours, the fibers are repeatedly dispersed and aggregated, forming uniform phyno balls.
最後にファイバーボールを充填材として成型する方法と
しては、ファイバーボールを製造した後バインダー繊維
が固着しない温度で乾燥し、乾燥後のファイバーボール
を空気か通過できる]くンチングプレート等からなる型
枠に充填し、熱風循環処理装置に導入し、バインダー繊
維の粘着温度以上9合成短繊維の融点未満で熱処理する
ことにより、ファイバーボール内部に点在するノ(イン
ダー繊維はその近傍の合成短繊維と接着し、ファイバー
ボール表面近傍にあるバインダー繊維はファイバーボー
ル間で接着し9強固でしかも柔軟な成型体となるのであ
る。Finally, the method of molding fiber balls as a filler is to dry them at a temperature that does not allow the binder fibers to stick after manufacturing the fiber balls, and then use a formwork made of a punching plate, etc. to allow air to pass through the dried fiber balls. By introducing the fiber into a hot air circulation treatment device and heat-treating it at a temperature higher than the adhesion temperature of the binder fiber and lower than the melting point of the synthetic short fiber, the fibers dotted inside the fiber ball (the binder fibers are separated from the synthetic short fibers in the vicinity). The binder fibers near the surface of the fiber balls adhere between the fiber balls to form a strong yet flexible molded body.
(実施例)
次に9本発明を実施例及び比較例により本発明を具体的
に説明する。(Examples) Next, the present invention will be specifically explained using nine examples and comparative examples.
なお、測定はクツション用軟質ウレタンフオームに関す
るJIS−に6401に準拠し、見掛は密度。The measurement is based on JIS-6401 regarding soft urethane foam for cushions, and the apparent density is measured.
圧縮残留ひずみ率、繰返し圧縮残留ひずみ率を測定した
。その他の測定法については次のとおりである。Compression residual strain rate and repeated compression residual strain rate were measured. Other measurement methods are as follows.
粘着温度
ポリマーが変形しはじめる温度であり、柳本自動融点測
定装置AMP −1型を使用し、シリコーンバス中での
ポリマーへの針入温度として求めた。Adhesive temperature This is the temperature at which the polymer begins to deform, and was determined as the needle penetration temperature into the polymer in a silicone bath using a Yanagimoto automatic melting point measuring device AMP-1.
極限粘度〔η〕
フェノールと四塩化エタン等重量混合溶媒を用いて20
°Cで測定した。Intrinsic viscosity [η] 20 using a mixed solvent of equal weights of phenol and tetrachloroethane
Measured at °C.
実施例1.比較例1〜4
イソフタル酸を20mo1% 共重合ポリエステル(粘
着温度200°C9〔η] = 0.69 )を鞘部と
し、ポリエチレンテレフタレートホモポリマー(融点2
57°C,Cη〕= 0.69 )を芯部に配し、複合
比1;1で公知の複合紡糸装置を用い、公知の条件下で
紡糸、延伸した後、捲縮を付与せずに第1表に示すバイ
ンダー繊維を得た。Example 1. Comparative Examples 1 to 4 20 mo1% isophthalic acid copolymerized polyester (adhesive temperature 200°C9 [η] = 0.69) was used as the sheath part, polyethylene terephthalate homopolymer (melting point 2
57°C, Cη] = 0.69) in the core, and after spinning and drawing under known conditions using a known composite spinning device at a composite ratio of 1:1, without crimp. Binder fibers shown in Table 1 were obtained.
また、前記ポリエチレンテレフタレートホモポリマーを
用いてl 4常の紡糸装置を用い、紡糸。Further, the polyethylene terephthalate homopolymer was used for spinning using a conventional spinning device.
延伸した後、捲縮を付与せずに第1表に示すポリエステ
ル繊維を得た。After stretching, polyester fibers shown in Table 1 were obtained without crimping.
第1表
第2表
上記バインダー繊維を20wt4.生体繊維8(hvt
チを適宜組合せ、第3図に示すファイバーボール製造装
置に5E/lKなるように投入し2回転数25Orpm
、 6時間で第2表に示す)丁イバーボールを得た。Table 1 Table 2 The above binder fiber was 20wt4. Biofiber 8 (HVT)
The fiber ball manufacturing equipment shown in Fig. 3 was put into the fiber ball manufacturing equipment at a ratio of 5E/lK, and the number of revolutions was 25Orpm.
In 6 hours, Dingiberballs (shown in Table 2) were obtained.
次に、上記実施例j1及び比較例1.2及び比較例4の
ファイバーボールを風乾した後、縦横300嘗、高さ5
0mの、熱風の通過性の良いパンチング板で作↓した型
枠に充填し、50b−の荷重をかげた際、高さか50冨
になるよう充填量を調整した後、220℃×5分間熱処
理した後、嵩密度、圧縮残留ひずみ率、繰り返し圧縮残
留ひずみ泥及び着用感を評価したところ、第3表のよう
であった。Next, after air-drying the fiber balls of Example j1, Comparative Example 1.2, and Comparative Example 4,
After filling a formwork made with a punched board with a diameter of 0 m and good permeability of hot air and applying a load of 50 b-, the amount of filling was adjusted so that the height would be 50 m, and then heat treated at 220°C for 5 minutes. After that, the bulk density, compression residual strain rate, repeated compression residual strain mud, and wearing feeling were evaluated, and the results were as shown in Table 3.
第3表
第4表
*着用感は上記サンプルの上4C30冒の1種Aの軟質
ウレタンフオームを乗せ、腰をおろした時の感触な○・
・良、X・・・不良として評価した。Table 3 Table 4 *The feeling of wearing is the feeling when you sit down with 4C30 Type 1 A soft urethane foam on top of the above sample.
- Good, X...Evaluated as poor.
実m例2,3.比較例5,6
笑Xi例1で用いたバインダ−10ジ及び生体繊維(イ
)の混綿比乞第4表のように変化させて実施?1」1と
同様にファイバーボールを&造し1こ力)、径及び収率
は実流例1と同様であった、このファイバーボールを実
施例1と同様に熱処理し、同一項目について評価ン行っ
た結果を第4表に示す。Actual examples 2 and 3. Comparative Examples 5 and 6 Comparison of the blend of binder 10 and biological fiber (A) used in Example 1. Comparisons were made with changes as shown in Table 4. 1 Fiber balls were made in the same manner as in Example 1 and the diameter and yield were the same as in Actual Example 1. This fiber ball was heat treated in the same manner as in Example 1 and evaluated for the same items. The results are shown in Table 4.
比較例7
生体繊維として実施例1で用いた生体4維(チに炬縮付
与し1こもの(重縮数]Oケ/25M、捲綿率21壬)
80wtチとビ→のバインダー繊維を混綿して。Comparative Example 7 4 biological fibers used in Example 1 as biological fibers (1 piece with crimp applied (number of condensations) O/25M, winding rate 21 mm)
Blend of 80wt chi and vinyl binder fibers.
実施でI]1と同様にファイバーボール化を試みたが。In practice, I tried to make it into a fiber ball in the same way as in 1.
生体4維か有″fる捲縮のため繊維か開よせず、ファイ
バーボールにはならなかっTこ。Because the four living fibers are crimped, the fibers do not open and do not form into a fiber ball.
比較例8
生体9L維としてユニチカ製中空複合轍紺13dX51
sw 80wt%とバインダー繊維としてユニチカル
メルティー(粘庸温度200℃>12dX51鰭20V
t%を常法により混綿、梳綿しウェッブとなした後、
50.!7/dの荷重をかけた際厚みが50目となる
よう積層した後、220°CX5分間熱処理を行い、所
定の寸法に裁断しサンプルと11.た。実施例と同様に
評価したところ、嵩密度25’y/m’s圧縮残留ひず
み率26チ、繰り返し圧縮残留ひずみ率18qbと圧縮
弾性能に乏しいものであった。Comparative Example 8 Hollow composite rut navy blue 13dX51 manufactured by Unitika as biological 9L fiber
sw 80wt% and unitary melty as binder fiber (viscosity temperature 200℃>12dX51 fin 20V
After blending and carding t% into a web using a conventional method,
50. ! After laminating the layers so that the thickness becomes 50 when a load of 7/d is applied, heat treatment is performed at 220°C for 5 minutes, and the samples are cut into predetermined dimensions. Ta. When evaluated in the same manner as in the examples, the bulk density was 25'y/m's, the compressive residual strain rate was 26 cm, and the repeated compressive residual strain rate was 18 qb, indicating that the compressive elastic performance was poor.
(発明の効果)
以上説明したように9本発明は特定の繊度、繊維長を有
する非捲縮の合成短繊維と、非捲縮のバインダー繊維を
特定の比率で混綿し、三次元のファイバーボール化した
ものを熱処理することにより、主体1維とバインダー璋
維が強固に接着するため、家具、ベツド等にふされしい
弾性回復性に優れた充填体であり、しかも繊維状である
ためフロン等の発泡剤を用いることもなく、またポリマ
ー中に窒素やイオウを含まないため、燃焼したとしても
有害ガスの発生がない等の利点を有するものである。(Effects of the Invention) As explained above, the present invention produces a three-dimensional fiber ball by blending non-crimped synthetic short fibers having a specific fineness and fiber length with non-crimping binder fibers in a specific ratio. By heat-treating the resulting material, the main fibers and the binder fibers firmly adhere to each other, making it a filling material with excellent elastic recovery suitable for furniture, beds, etc. Moreover, since it is fibrous, it is free from fluorocarbons, etc. It does not require any blowing agents, and since the polymer does not contain nitrogen or sulfur, it has the advantage that no harmful gas is generated even if it is burned.
第1図は本発明であるファイバーボールの概観図で、(
イ)は真球形状、(ロ)は扁平球状を示し、第2図はフ
ァイバーボールの拡大図、第3図はファイバーボールの
製造装置を示す。
図中、1は主体繊維、2はバインダー繊維、3は水槽、
4は攪拌翼、5は邪魔板、6はモーターを示す。Figure 1 is an overview of the fiber ball of the present invention.
(a) shows a true spherical shape, (b) shows a flat spherical shape, FIG. 2 is an enlarged view of the fiber ball, and FIG. 3 shows the fiber ball manufacturing apparatus. In the figure, 1 is the main fiber, 2 is the binder fiber, 3 is the water tank,
4 is a stirring blade, 5 is a baffle plate, and 6 is a motor.
Claims (2)
質的に捲縮を有しない合成短繊維(A)と,繊度3〜3
0デニール,長さ10〜70mmの実質的に捲縮を有せ
ず,しかも前記合成短繊維(A)と相溶性を有し,合成
短繊維(A)の融点より20℃以上低い粘着温度を有す
るバインダー繊維(B)が重量比で90〜50%/10
〜50%の割合でブレンドされた平均径5〜50mmで
ある詰綿用ファイバーボール。(1) Synthetic short fibers (A) with a fineness of 3 to 30 deniers and a length of 10 to 70 mm that have virtually no crimp, and a fineness of 3 to 3
0 denier, has a length of 10 to 70 mm, has substantially no crimp, is compatible with the synthetic short fiber (A), and has a sticking temperature that is 20° C. or more lower than the melting point of the synthetic short fiber (A). The binder fiber (B) has a weight ratio of 90 to 50%/10
Fiber balls for filling having an average diameter of 5 to 50 mm blended at a ratio of ~50%.
し単位主体のポリエステルであり,バインダー(B)が
低融点ポリエステルである請求項1記載の詰綿用ファイ
バーボール。(2) The fiber ball for stuffing according to claim 1, wherein the synthetic short fibers (A) are polyester mainly containing ethylene terephthalate repeating units, and the binder (B) is a low melting point polyester.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8195690A JP2948259B2 (en) | 1990-03-29 | 1990-03-29 | Fiber ball for filling |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8195690A JP2948259B2 (en) | 1990-03-29 | 1990-03-29 | Fiber ball for filling |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03287847A true JPH03287847A (en) | 1991-12-18 |
JP2948259B2 JP2948259B2 (en) | 1999-09-13 |
Family
ID=13760954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8195690A Expired - Fee Related JP2948259B2 (en) | 1990-03-29 | 1990-03-29 | Fiber ball for filling |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2948259B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010096079A (en) * | 2000-04-17 | 2001-11-07 | 고동현 | Manufacturing method of bed-clothes wadding |
JP2002242061A (en) * | 2001-02-15 | 2002-08-28 | Nippon Ester Co Ltd | Ball-shaped fiber including thermobonding fiber and having biodegradability, and fiber structure |
JP2015155586A (en) * | 2014-02-21 | 2015-08-27 | ダイワボウホールディングス株式会社 | Granulated wool and padding material using the same, and bed/bedding or clothing including the padding material |
CN108070956A (en) * | 2016-11-07 | 2018-05-25 | 财团法人纺织产业综合研究所 | non-woven fabric structure and manufacturing method thereof |
WO2019123147A1 (en) * | 2017-12-21 | 2019-06-27 | 3M Innovative Properties Company | Thermal insulation filling material, preparation method thereof, and thermal insulation article |
-
1990
- 1990-03-29 JP JP8195690A patent/JP2948259B2/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010096079A (en) * | 2000-04-17 | 2001-11-07 | 고동현 | Manufacturing method of bed-clothes wadding |
JP2002242061A (en) * | 2001-02-15 | 2002-08-28 | Nippon Ester Co Ltd | Ball-shaped fiber including thermobonding fiber and having biodegradability, and fiber structure |
JP2015155586A (en) * | 2014-02-21 | 2015-08-27 | ダイワボウホールディングス株式会社 | Granulated wool and padding material using the same, and bed/bedding or clothing including the padding material |
CN108070956A (en) * | 2016-11-07 | 2018-05-25 | 财团法人纺织产业综合研究所 | non-woven fabric structure and manufacturing method thereof |
WO2019123147A1 (en) * | 2017-12-21 | 2019-06-27 | 3M Innovative Properties Company | Thermal insulation filling material, preparation method thereof, and thermal insulation article |
Also Published As
Publication number | Publication date |
---|---|
JP2948259B2 (en) | 1999-09-13 |
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