JP2004324010A - Tufted carpet base fabric - Google Patents

Tufted carpet base fabric Download PDF

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Publication number
JP2004324010A
JP2004324010A JP2003120989A JP2003120989A JP2004324010A JP 2004324010 A JP2004324010 A JP 2004324010A JP 2003120989 A JP2003120989 A JP 2003120989A JP 2003120989 A JP2003120989 A JP 2003120989A JP 2004324010 A JP2004324010 A JP 2004324010A
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Japan
Prior art keywords
base fabric
formaldehyde
carpet base
filament
needle
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JP2003120989A
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Japanese (ja)
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JP4106619B2 (en
Inventor
Shintaro Yamazaki
申太郎 山崎
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Toyobo Co Ltd
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Toyobo Co Ltd
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  • Nonwoven Fabrics (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a filament nonwoven fabric material, utilizable for applications in which occurrence of formaldehyde becomes a problem, having low release amount of formaldehyde to the environmental air and suitable for a tufted carpet base fabric, particularly for automobiles. <P>SOLUTION: The tufted carpet base fabric has 1.5-3.5 dtex fineness of filament and 3-30 mass% binder resin content and 70-200 g/m<SP>2</SP>basis weight and ≤0.50 μg formaldehyde amount released in the filament nonwoven fabric composed of synthetic resin filaments and a binder component for mutually fixing the filaments. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
本発明は、合成樹脂フィラメントと、該フィラメントを互いに固定させる能力をもつバインダー成分とで構成され、カーペットや床材の基布に好適な長繊維不織布に関するものであり、さらに詳しくは、自動車用カーペットに好適な基布に関するものである。
【0002】
【従来の技術】
長繊維不織布において繊維間を接着し固定する方法として、バインダー成分を用いる方法が広く採用され、 バインダー成分としては、エマルジョンタイプの接着用樹脂を使用する方法が最も一般的であり、自己架橋性樹脂を架橋させることや反応性基含有樹脂と架橋剤を併用することが幅広く用いられている。これらの架橋成分は、メチロール基であり、ホルムアルデヒド発生の原因となる。
【0003】
さて近年、 環境の空気質とアレルギー等の各種疾患との関連に社会の関心が高まってきており、住宅に於ける室内空気汚染問題はシックハウス症候群、シックビルディング症候群等の症例として取り上げられているが、室内空気汚染物質としてホルムアルデヒド、揮発性有機化合物(VOC)等が問題となっている。
特にホルムアルデヒドに関しては、1997年に厚生省(当時)から住宅におけるガイドライン値が発表されるなど、明確に問題視されてきており、その発生源は、住宅建築材料である木材、合板、内装材に使われる接着剤、防腐剤、防蟻剤、 生活空間内の家具・調度品、生活用品、および業務用事務機器等あらゆる分野に渡っている。
ホルムアルデヒド対策として、ホルムアルデヒド吸着剤を具備させる方法(特許文献1など)やホルムアルデヒド吸着剤をコーティングする方法(特許文献2など)などが知られているが、十分な対策にはなっていない。
【0004】
【特許文献1】
特開平11−046965号公報
【特許文献2】
特開2000−287819号公報
【0005】
【発明が解決しようとする課題】
本発明は、環境の空気質への影響を考慮せざるを得なくなった現在の情勢に合致すべく、生活用品、産業資材、建築材料、土木資材等のさまざまな分野において、将来規制されるであろうホルムアルデヒド環境基準に適合させる用途に利用可能な、環境の空気へのホルムアルデヒドの放出量が低く、特に自動車用のタフトカーペット基布に好適な長繊維不織布材料を提供しようとするものである。
【0006】
【課題を解決するための手段】
すなわち、本発明は以下の構成を採用する。
1.合成樹脂フィラメントと、該フィラメントを互いに固定させるバインダー成分とで構成される長繊維不織布において、フィラメントの繊度が1.5〜3.5デシテックス、 バインダー樹脂の含有率が3〜30質量%、目付が70〜200g/ mであり、放出されるホルムアルデヒドの量が0.50μg以下であることを特徴とするタフトカーペット基布。
2.合成樹脂フィラメントが、互いに熱及び圧力によって固定された後、さらにバインダー成分によって固定されてなることを特徴とする前項1に記載のタフトカーペット基布。
3.合成樹脂フィラメントが、ニードルパンチによって互いに絡められた後、さらにバインダー成分によって固定されてなることを特徴とする前項1に記載のタフトカーペット基布。
4.合成樹脂フィラメントが、ニードルパンチによって互いに絡められた後、バインダー成分によって固定され、その後、さらに熱及び圧力によって固定されてなることを特徴とする前項1に記載のタフトカーペット基布。
【0007】
【発明の実施の形態】
本発明における長繊維不織布は、スパンボンド法等の従来公知の製造方法によって得られる長繊維不織布であり、多数のノズル孔をもつ紡糸口金からの溶融紡糸されたフィラメントを主たる構成材料とするものである。
本発明におけるフィラメントを形成する合成樹脂とは、ポリエステル、ナイロン、ポリプロピレンなどの公知の合成繊維材料を用いることができるが、リサイクルのしやすさ、耐熱性などの観点から、ポリエチレンテレフタレート、ポリブチレンテレフタレート等のホモポリエステルやこれらの成分以外に共重合成分を有する公知の共重合ポリエステルなどの一般的なポリエステルが好ましい。
これらの合成樹脂材料には安定剤、紫外線吸収剤、吸湿剤、滑剤、顔料等が含まれても良いが、これらにホルムアルデヒドの発生源を有することは好ましくない。
【0008】
合成樹脂フィラメントの繊度は1.5〜3.5dtexである。繊度が1.5dtexより小さい場合は糸切れを引き起こし、その操業性の悪化要因となる他、繊維の接着点数や接着点密度が増し、タフティングの際に接着点の破壊及び繊維の切断による引張り強力の低下が大きくなり、かつタフティングの際の針の貫通抵抗が過大になる。また反対に繊度が3.5dtexより大きいと、目が大きくなり、タフト針の貫通抵抗は低くなるが、パイル糸の保持力低下し、また、繊維の絡み及び接点が減少し強度が低下する。
【0009】
紡出されたフィラメントはコンベアネットなどで捕集されてウエブを形成し、該ウエブのフィラメントは、必要によりエンボスカレンダーなどによる加熱、圧着処理、ニードルパンチなどによる絡合処理、バインダー樹脂処理などの種々の接合手段によって接合される。
【0010】
エンボスカレンダーによる加熱温度は、合成樹脂の融点−15℃から−80℃の範囲が好ましく、ポリエステルの場合は、180〜250℃が好ましく、より好ましくは200〜230℃である。この処理により、後のバインダー成分で固定する工程でのシートの搬送性が安定する、シートを薄くできる等の効果が得られる。
【0011】
ニードルパンチによる絡合処理をする場合は、ニードルパンチングの針密度は、ニードルパンチング用針の形状や挿入深さによって20〜160回/cmの範囲内に設定されるのが好ましく、更には60〜120回/cmが好ましい。上記針密度が20回/cm未満の場合には、ニードルパンチングの効果がなく、強伸度が著しく低下するためその後の加工工程で歪みが発生し、シワ等の要因となる。また反対に160回/cmを超えた場合、繊維や、接着点の切断が激しく、強力が低下する。
【0012】
ニードルパンチによる繊維の絡み状態の調整により、シートが厚くできる、シートを薄くできる、厚さ方向にシートが剥離しにくくなる、等の特徴を付与できる。バインダー樹脂処理する前のシートの目付は60〜150g/ m、好ましくは80〜120g/ mである。この不織布ウェッブの目付量が60g/ m未満の場合には、タフトカーペット用基布として必要な引張り強力や5%伸張時応力などの物性が得られず、製品カーペットの寸法安定性が低くなる。反対に目付量が大きすぎると、過剰物性となって基布として不経済となるばかりでなく、目付増加による厚みの増加で消費パイル糸も増え、製品としても不経済である。また、厚みが増すことにより、バッキング材の基布への入り込みが低下し、これにより製品のキャスター性が低下するという問題もかかえることになる。
【0013】
バインダー樹脂処理は、噴霧、浸漬、コーティングなどを適宜選択できるが、上記のエンボスカレンダー処理やニードルパンチング処理されたウエブをバインダー樹脂処理浴中に浸漬後、絞るパッド・ニップ法が好ましい。
【0014】
バインダー樹脂としては、ポリエステル樹脂水系エマルジョン、アクリル樹脂水系エマルジョンなどでホルマリンや有機溶剤などのVOCの発生源にならないものが好ましい。 エマルジョンタイプの樹脂に、触媒、PH調整剤、浸透剤、消泡剤、分散剤等の助剤を併用することができるが、これらにホルムアルデヒドの発生源にならないものが好ましい。
【0015】
バインダー樹脂液が付与された後は、通常80〜130℃程度の温度で乾燥し、次いで130〜200℃で1〜10分間、好ましくは150〜180℃で1〜5分間のベーキング処理をする。ベーキング処理することで、VOCを著しく低減させることができる。
【0016】
バインダー樹脂の固形分付与量は、全基布質量に対して3〜30質量%であり、好ましくは5〜15質量%である。バインダー樹脂の固形分付与量が5質量%未満の場合には、製品の引張り強さが不足し、30質量%を超えた場合は、タフティングの際にタフティング用針の貫通抵抗が大きく、また構成繊維の切断による物性の低下が甚だしく、二次加工性及び製品後の寸法安定性を低下させる。
【0017】
バインダー樹脂加工後に、さらに、カレンダーローラー等の熱及び圧力を作用させて、フィラメント間の固定をより強固にしたり、シート表面のバインダー樹脂を平滑化したり、エンボスパターンを付与することができる。
カーペット基布としての目付は、70〜200g/ mであり、放出されるホルムアルデヒドの量が0.50μg以下である。
本発明における放出されるホルムアルデヒドの量とは、以下の方法で測定されるものである。
【0018】
すなわち、一時間あたりの通気量12リットルの温度70℃の窒素ガス流雰囲気下において面積500cmの長繊維不織布から窒素ガス12リットル中に放出されるホルムアルデヒドの量である。すなわち、測定試料の一定質量に対してではなく、一定面積からのホルムアルデヒド発生量を測定するものであり、使用空間に面する壁、床、天井、その他物品の特定面積からの室内空気汚染の影響を受ける使用者の現実の利用状況にできるだけ近い形で評価するものである。
【0019】
本発明は、この分野ではほとんど実用的に用いられなかったノンホルマリンのバインダー樹脂の使用と適切な繊度低減を組み合わせる事によって、ニードルパンチでの繊維の絡みの増大や、フィラメント間の接点増大効果を狙うことにより、従来のホルマリン由来の架橋剤を使用した場合と遜色ない物性と加工性を確保することができる。逆に、従来のホルマリン系バインダー樹脂では、長繊維不織布の繊度を小さくすると、バインダーの結合が強過ぎ、 タフト加工性が損なわれるが、本発明では、このような欠点は認められない。
本発明のカーペット基布のタフティング時のタフト針の貫通抵抗は、8N以下であることが好ましく、より好ましくは、6N以下である。
【0020】
【実施例】
以下に、本発明を実施例によって説明するが、本発明は何らこれらに限定されるものではない。
▲1▼ホルムアルデヒド発生量は次の方法:
長繊維不織布5cm×10cm×10片を採取容器にとる。
採取容器内温度=70℃で高純度窒素ガスを0.2ml/minの速度で流入させ、市販のDNPH(2,4−ジニトロフェニルヒドラジン)カートリッジに1時間12リットル通し、発生したホルムアルデヒドをDNPH誘導体化し固相吸着させる。 カートリッジからアセトニトリル5mlでホルムアルデヒドDNPH誘導体を抽出し、試料溶液を作成する。
試料溶液を高速液体クロマトグラフ(HPLC):Hewlett−Packard社製HP1100:に導入し分析する。
その他のHPLC分析条件は、カラム:Waters社製μBondapak C18 10μm 125Å 3.9mm×150mm、移動相:水/アセトニトリル=45/55、流速=0.8ml/min、検出:UV 360nm。
以上より、一時間あたりの通気量12リットルの温度70℃の窒素ガス流雰囲気下において面積500cmの長繊維不織布から窒素ガス12リットル中に放出されるホルムアルデヒドの量を求める。
【0021】
▲2▼貫通抵抗:
得られたカーペット用基布を円形土台の上にベルトで固定し、エー・アンド・デイ社製RTC−1250測定器の上側チャックにタフティング針を一本設置し、それを用いて土台上のタフテッドカーペット用基布に穿孔し、その際の荷重(N)を測定した。なお、タフト針はSNF Spezialnadelfabrik社製 0556FLを用いた。
【0022】
▲3▼タフト性評価:
得られたカーペット用基布に920デニールのナイロン製パイル糸を用いてゲージ8本/1インチ、ステッチ数8/1インチ、ループパイルの高さ4mmの条件でタフティングを行い、タフト性の評価を行なった。
【0023】
[実施例1]
ポリエチレンテレフタレートを溶融紡糸し、スパンボンド法により単糸繊度を2.2dtexのフィラメントでウエブを形成し、ニードルパンチ加工(針密度65回/cm、針深さ10mm)を施した後、ノンホルマリンタイプのアクリル樹脂:大日本インキ化学工業社製 VONCOAT ED−85及び平滑剤としてシリコン樹脂エマルジョンである大日本インキ化学工業社製 DIC−SILICONE−SOFTNER 300の調合液をパッド・ニップして乾燥後、160℃で3分間ベーキングし、目付100g/ mでバインダー成分の付与量が10質量%の基布を得た。この基布を前述の方法でホルムアルデヒド発生量を測定した結果、ホルムアルデヒド発生量は0.29μgであった。また、タフト針貫通抵抗は5Nであった。
さらに、得られた基布について、タフト性を評価したところ、何ら問題がなかった。
【0024】
[実施例2]
ポリエチレンテレフタレートを溶融紡糸し、スパンボンド法により単糸繊度を3.9dtexのフィラメントでウエブを形成し、ニードルパンチ加工(針密度65回/cm、針深さ10mm)に続き、エンボスローラーで熱接着(200℃)した後、ホルムアルデヒドフリータイプの自己架橋型アクリル樹脂(BASFディスパージョン社製 アクロナール2348)及び実施例1と同じ平滑剤にて実施例1と同様にパッド・ニップ・ベーキング方式で固定化処理した後、さらにカレンダーローラーで熱圧着(205℃)し、目付160g/ mでバインダー成分の付与量が15%の基布を得た。
この基布を前述の方法でホルムアルデヒド発生量を測定した結果、ホルムアルデヒド発生量は0.44μgであった。タフト針貫通抵抗は6Nであった。
さらに、得られた基布について、タフト性を評価したところ、何ら問題がなかった。
【0025】
[比較例1]
ポリエチレンテレフタレートを溶融紡糸し、スパンボンド法により単糸繊度を3.9dtexのフィラメントでウエブを形成し、エンボスローラーで熱接着した後、一般的な架橋反応性をもつアクリル樹脂および架橋剤としてメラミン樹脂、触媒として3級アミンからなる調合液にて実施例1と同様にパッド・ニップ・ベーキング方式で固定化処理した後、さらにカレンダーローラーで熱圧着(205℃)し、目付100g/ mでバインダー成分の付与量が10%の基布を得た。
この基布を前述の方法でホルムアルデヒド発生量を測定した結果、ホルムアルデヒド発生量は9.17μgであった。タフト針貫通抵抗は12Nであった。
【0026】
[比較例2]
実施例1において、単糸繊度を4.0dtexとした以外は、実施例1と同様にして基布を得た。さらに、得られた基布について、タフト性を評価したところ、パイル糸の保持力が低く、また、基布としての特性に劣るものであった。
【0027】
【発明の効果】
本発明によれば、環境へのホルムアルデヒドの放出量が低く、かつタフト性に優れたカーペット用基布を提供でき、この基布は、特に自動車のカーペット用に好適である。
[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a long-fiber nonwoven fabric composed of a synthetic resin filament and a binder component capable of fixing the filament to each other, and suitable for a base fabric of a carpet or a flooring material. To a suitable base fabric.
[0002]
[Prior art]
A method using a binder component is widely adopted as a method for bonding and fixing fibers in a long-fiber nonwoven fabric. As a binder component, a method using an emulsion-type adhesive resin is the most common, and a self-crosslinkable resin is used. Are widely used in combination with a reactive group-containing resin and a crosslinking agent. These crosslinking components are methylol groups and cause formaldehyde generation.
[0003]
In recent years, there has been increasing public interest in the relationship between environmental air quality and various diseases such as allergies, and the problem of indoor air pollution in houses has been taken up as cases of sick house syndrome and sick building syndrome. In addition, formaldehyde, volatile organic compounds (VOC) and the like have become problems as indoor air pollutants.
In particular, regarding formaldehyde, the Ministry of Health and Welfare issued a guideline value for housing in 1997, and it has been clearly identified as a problem, and its source is used for wood, plywood, and interior materials, which are home building materials. It covers a wide range of fields, including adhesives, preservatives, termites, furniture and furniture in living spaces, daily necessities, and office equipment for business use.
As a formaldehyde countermeasure, a method of providing a formaldehyde adsorbent (Patent Document 1 and the like) and a method of coating a formaldehyde adsorbent (Patent Document 2 and the like) are known, but they are not sufficient measures.
[0004]
[Patent Document 1]
Japanese Patent Application Laid-Open No. H11-046965 [Patent Document 2]
JP 2000-287819 A
[Problems to be solved by the invention]
The present invention will be regulated in various fields such as daily necessities, industrial materials, building materials, civil engineering materials, etc. in order to conform to the current situation in which the influence on the air quality of the environment must be considered. It is an object of the present invention to provide a long-fiber nonwoven material which has a low formaldehyde emission into the environment air and is suitable for a tufted carpet base fabric for automobiles, which can be used for an application which conforms to formaldehyde environmental standards.
[0006]
[Means for Solving the Problems]
That is, the present invention employs the following configuration.
1. In a long-fiber nonwoven fabric composed of synthetic resin filaments and a binder component for fixing the filaments to each other, the fineness of the filaments is 1.5 to 3.5 decitex, the binder resin content is 3 to 30% by mass, and the areal weight. A tufted carpet base fabric, which has a formaldehyde content of 70 to 200 g / m 2 and an amount of released formaldehyde of 0.50 μg or less.
2. 2. The tufted carpet base fabric according to the above item 1, wherein the synthetic resin filaments are fixed to each other by heat and pressure, and further fixed by a binder component.
3. 2. The tufted carpet base fabric according to the above item 1, wherein the synthetic resin filaments are entangled with each other by a needle punch, and further fixed by a binder component.
4. 2. The tufted carpet base fabric according to the above item 1, wherein the synthetic resin filaments are entangled with each other by a needle punch, fixed by a binder component, and further fixed by heat and pressure.
[0007]
BEST MODE FOR CARRYING OUT THE INVENTION
The long-fiber nonwoven fabric in the present invention is a long-fiber nonwoven fabric obtained by a conventionally known manufacturing method such as a spunbonding method, and is mainly composed of a melt-spun filament from a spinneret having a large number of nozzle holes. is there.
As the synthetic resin forming the filament in the present invention, known synthetic fiber materials such as polyester, nylon, and polypropylene can be used, but polyethylene terephthalate, polybutylene terephthalate, etc. General polyesters such as homopolyesters and known polyesters having a copolymerization component in addition to these components are preferred.
These synthetic resin materials may contain a stabilizer, an ultraviolet absorber, a moisture absorbent, a lubricant, a pigment, and the like, but it is not preferable that these materials have a source of formaldehyde.
[0008]
The fineness of the synthetic resin filament is 1.5 to 3.5 dtex. If the fineness is smaller than 1.5 dtex, thread breakage is caused, and the operability is deteriorated. In addition, the number of bonded points and the density of bonded points are increased, and the breaking of the bonded points and the pulling due to the cutting of the fibers at the time of tufting. The drop in strength is large, and the penetration resistance of the needle during tufting becomes excessive. On the other hand, when the fineness is larger than 3.5 dtex, the eyes become large and the penetration resistance of the tuft needle becomes low, but the holding power of the pile yarn is reduced, and the entanglement of fibers and the contact point are reduced, so that the strength is reduced.
[0009]
The spun filaments are collected by a conveyor net or the like to form a web, and the filaments of the web are subjected to various processes such as heating by an emboss calender, pressure bonding, entanglement by a needle punch, binder resin treatment, etc. Are joined by joining means.
[0010]
The heating temperature by the emboss calendar is preferably in the range of −15 ° C. to −80 ° C. of the melting point of the synthetic resin, and in the case of polyester, it is preferably 180 to 250 ° C., and more preferably 200 to 230 ° C. By this treatment, effects such as stabilization of sheet transportability in the subsequent step of fixing with the binder component and reduction of the thickness of the sheet can be obtained.
[0011]
When performing the entanglement treatment by needle punching, the needle density of the needle punching is preferably set in the range of 20 to 160 times / cm 2 depending on the shape and insertion depth of the needle for needle punching, and more preferably 60 to 60 times / cm 2. ~ 120 times / cm 2 is preferred. When the needle density is less than 20 needles / cm 2 , there is no effect of needle punching, and the strength and elongation are significantly reduced, so that distortion occurs in a subsequent processing step, which causes wrinkles and the like. On the other hand, if it exceeds 160 times / cm 2 , the fibers and the bonding points are severely cut, and the strength is reduced.
[0012]
By adjusting the entangled state of the fibers by the needle punch, it is possible to impart characteristics such as a thicker sheet, a thinner sheet, and a difficulty in peeling the sheet in the thickness direction. The basis weight of the sheet before the binder resin treatment is 60 to 150 g / m 2 , preferably 80 to 120 g / m 2 . If the basis weight of this nonwoven fabric web is less than 60 g / m 2 , physical properties such as tensile strength and stress at 5% elongation required as a base fabric for tufted carpet cannot be obtained, and the dimensional stability of the product carpet becomes low. . On the other hand, if the basis weight is too large, not only the excess physical properties will be uneconomical as a base fabric, but also the consumption of pile yarn will increase due to the increase in the thickness due to the increase in the basis weight, which is uneconomical as a product. In addition, an increase in the thickness causes a problem that penetration of the backing material into the base fabric is reduced, and thereby, the castability of the product is reduced.
[0013]
As the binder resin treatment, spraying, dipping, coating and the like can be appropriately selected. However, the pad-nip method in which the above-mentioned embossed calender or needle punched web is dipped in a binder resin treatment bath and then squeezed is preferable.
[0014]
As the binder resin, a polyester resin aqueous emulsion, an acrylic resin aqueous emulsion, or the like that does not become a source of VOC such as formalin or an organic solvent is preferable. Auxiliary agents such as a catalyst, a pH adjuster, a penetrant, an antifoaming agent, and a dispersant can be used in combination with the emulsion type resin, but those which do not generate formaldehyde are preferred.
[0015]
After the binder resin liquid has been applied, drying is usually performed at a temperature of about 80 to 130 ° C, followed by baking at 130 to 200 ° C for 1 to 10 minutes, preferably 150 to 180 ° C for 1 to 5 minutes. By performing the baking process, VOC can be significantly reduced.
[0016]
The solid content of the binder resin is 3 to 30% by mass, preferably 5 to 15% by mass, based on the total mass of the base fabric. When the solid content of the binder resin is less than 5% by mass, the tensile strength of the product is insufficient, and when it exceeds 30% by mass, the penetration resistance of the tufting needle during tufting is large, Further, the physical properties are significantly reduced due to the cutting of the constituent fibers, and the secondary workability and the dimensional stability after the product are reduced.
[0017]
After the processing of the binder resin, heat and pressure of a calender roller or the like are further applied to strengthen the fixing between the filaments, smooth the binder resin on the sheet surface, or impart an emboss pattern.
The basis weight as a carpet base fabric is 70 to 200 g / m 2 , and the amount of formaldehyde released is 0.50 μg or less.
The amount of formaldehyde released in the present invention is measured by the following method.
[0018]
That is, this is the amount of formaldehyde released from the long-fiber nonwoven fabric having an area of 500 cm 2 into 12 liters of nitrogen gas under a nitrogen gas flow atmosphere at a temperature of 70 ° C. with an air flow rate of 12 liters per hour. In other words, it measures the amount of formaldehyde generated from a certain area, not from a certain mass of the measurement sample, and the effect of indoor air pollution from a specific area of the wall, floor, ceiling, and other articles facing the working space. The evaluation is performed in a form as close as possible to the actual usage situation of the user receiving the information.
[0019]
The present invention combines the use of a non-formalin binder resin, which has hardly been practically used in this field, with an appropriate reduction in fineness, thereby increasing the entanglement of fibers in the needle punch and the effect of increasing the contact points between filaments. By aiming, it is possible to secure physical properties and workability comparable to the case where a conventional formalin-derived cross-linking agent is used. Conversely, in the conventional formalin-based binder resin, if the fineness of the long-fiber nonwoven fabric is reduced, the binding of the binder is too strong and the tufting property is impaired. However, such a defect is not recognized in the present invention.
The penetration resistance of the tuft needle at the time of tufting of the carpet base fabric of the present invention is preferably 8N or less, more preferably 6N or less.
[0020]
【Example】
Hereinafter, the present invention will be described with reference to examples, but the present invention is not limited thereto.
(1) The amount of formaldehyde generated is determined by the following method:
Take 5 cm × 10 cm × 10 pieces of long fiber non-woven fabric in a sampling container.
High-purity nitrogen gas was introduced at a rate of 0.2 ml / min at a temperature of the collection container of 70 ° C. and passed through a commercially available DNPH (2,4-dinitrophenylhydrazine) cartridge for 12 hours for 1 hour. And solid phase adsorption. A formaldehyde DNPH derivative is extracted from the cartridge with 5 ml of acetonitrile to prepare a sample solution.
The sample solution is introduced into a high performance liquid chromatograph (HPLC): HP1100 manufactured by Hewlett-Packard, and analyzed.
Other HPLC analysis conditions are as follows: Column: μBondapak C18 10 μm 125Å3.9 mm × 150 mm manufactured by Waters, mobile phase: water / acetonitrile = 45/55, flow rate = 0.8 ml / min, detection: UV 360 nm.
From the above, the amount of formaldehyde released into 12 liters of nitrogen gas from a long-fiber nonwoven fabric having an area of 500 cm 2 in an atmosphere of nitrogen gas at a temperature of 70 ° C. with an air flow rate of 12 liters per hour is determined.
[0021]
(2) Penetration resistance:
The obtained carpet base fabric was fixed on a circular base with a belt, and one tufting needle was set on the upper chuck of an A & D RTC-1250 measuring instrument. The tufted carpet base fabric was perforated, and the load (N) at that time was measured. The tuft needle used was 0556FL manufactured by SNF Specialized Nadfabrik.
[0022]
(3) Tuft property evaluation:
Tufting is performed on the obtained carpet base fabric using 920 denier nylon pile yarn under the conditions of a gauge of 8/1 inch, a stitch number of 8/1 inch, and a loop pile height of 4 mm, to evaluate the tufting property. Was performed.
[0023]
[Example 1]
Polyethylene terephthalate is melt spun, a web is formed with a filament having a single yarn fineness of 2.2 dtex by a spun bond method, and subjected to needle punching (needle density 65 times / cm 2 , needle depth 10 mm) and then non-formalin Acrylic resin of the type: VONCOAT ED-85 manufactured by Dainippon Ink and Chemicals, and DIC-SILICONE-SOFTNER 300 manufactured by Dainippon Ink and Chemicals, which is a silicone resin emulsion as a smoothing agent, are pad-nip-dried and dried. The resultant was baked at 160 ° C. for 3 minutes to obtain a base cloth having a basis weight of 100 g / m 2 and an applied amount of a binder component of 10% by mass. As a result of measuring the amount of formaldehyde generated from this base fabric by the method described above, the amount of formaldehyde generated was 0.29 μg. The tuft needle penetration resistance was 5N.
Furthermore, when the tuft property of the obtained base fabric was evaluated, there was no problem at all.
[0024]
[Example 2]
Polyethylene terephthalate is melt spun, a web is formed with a filament having a single yarn fineness of 3.9 dtex by a spun bond method, followed by needle punching (needle density 65 times / cm 2 , needle depth 10 mm), followed by heat with an emboss roller. After adhering (200 ° C.), it is fixed with a form-free type self-crosslinking acrylic resin (Acronal 2348 manufactured by BASF Dispersion Co., Ltd.) and the same smoothing agent as in Example 1 by the pad nip baking method as in Example 1. After the heat treatment, the resultant was further subjected to thermocompression bonding (205 ° C.) with a calendar roller to obtain a base cloth having a basis weight of 160 g / m 2 and a binder component application amount of 15%.
As a result of measuring the amount of formaldehyde generated from this base fabric by the method described above, the amount of formaldehyde generated was 0.44 μg. The tuft needle penetration resistance was 6N.
Furthermore, when the tuft property of the obtained base fabric was evaluated, there was no problem at all.
[0025]
[Comparative Example 1]
Polyethylene terephthalate is melt spun, a web is formed with a filament having a single fiber fineness of 3.9 dtex by a spun bond method, and thermally bonded with an emboss roller, and then an acrylic resin having a general crosslinking reactivity and a melamine resin as a crosslinking agent are used. Then, the mixture was fixed by a pad nip baking method in the same manner as in Example 1 using a preparation solution containing a tertiary amine as a catalyst, and then subjected to thermocompression bonding (205 ° C.) with a calender roller, and a binder having a basis weight of 100 g / m 2 . A base cloth having a component application amount of 10% was obtained.
As a result of measuring the amount of formaldehyde generated from this base fabric by the method described above, the amount of formaldehyde generated was 9.17 μg. The tuft needle penetration resistance was 12N.
[0026]
[Comparative Example 2]
A base fabric was obtained in the same manner as in Example 1 except that the single-fiber fineness was set to 4.0 dtex. Further, when the tuft property of the obtained base fabric was evaluated, it was found that the holding power of the pile yarn was low and the properties as the base fabric were inferior.
[0027]
【The invention's effect】
ADVANTAGE OF THE INVENTION According to this invention, the amount of formaldehyde discharge | release to environment can be provided and the base fabric for carpets excellent in tuft property can be provided, and this base fabric is suitable especially for carpet of a motor vehicle.

Claims (4)

合成樹脂フィラメントと、該フィラメントを互いに固定させるバインダー成分とで構成される長繊維不織布において、フィラメントの繊度が1.5〜3.5dtex、 バインダー樹脂の含有率が3〜30質量%、目付が70〜200g/ mであり、放出されるホルムアルデヒドの量が0.50μg以下であることを特徴とするタフトカーペット基布。In a long-fiber nonwoven fabric composed of a synthetic resin filament and a binder component for fixing the filament to each other, the filament fineness is 1.5 to 3.5 dtex, the binder resin content is 3 to 30% by mass, and the basis weight is 70. -200 g / m < 2 > and the amount of formaldehyde released is 0.50 [mu] g or less. 合成樹脂フィラメントが、互いに熱及び圧力によって固定された後、さらにバインダー成分によって固定されてなることを特徴とする請求項1に記載のタフトカーペット基布。The tuft carpet base fabric according to claim 1, wherein the synthetic resin filaments are fixed to each other by heat and pressure, and then further fixed by a binder component. 合成樹脂フィラメントが、ニードルパンチによって互いに絡められた後、さらにバインダー成分によって固定されてなることを特徴とする請求項1に記載のタフトカーペット基布。The tufted carpet base fabric according to claim 1, wherein the synthetic resin filaments are entangled with each other by a needle punch, and further fixed by a binder component. 合成樹脂フィラメントが、ニードルパンチによって互いに絡められた後、バインダー成分によって固定され、その後、さらに熱及び圧力によって固定されてなることを特徴とする請求項1に記載のタフトカーペット基布。The tuft carpet base fabric according to claim 1, wherein the synthetic resin filaments are entangled with each other by a needle punch, fixed by a binder component, and further fixed by heat and pressure.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007224493A (en) * 2007-03-29 2007-09-06 Toyobo Co Ltd Tuft carpet base fabric

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63227852A (en) * 1987-03-02 1988-09-22 エア・プロダクツ・アンド・ケミカルズ・インコーポレイテツド Binder for nonwoven fabric
JPH02251656A (en) * 1989-03-16 1990-10-09 Natl Starch & Chem Corp Thermo-resistant binder for non-woven fablic not containing formaldehyde
JPH0931818A (en) * 1995-07-20 1997-02-04 Toray Ind Inc Primary backing fabric for tufted carpet, its production and tufted carpet
JPH10216002A (en) * 1997-02-05 1998-08-18 Unitika Ltd Primary foundation for tile carpet and manufacture thereof
JP2000506940A (en) * 1996-02-21 2000-06-06 ビーエーエスエフ アクチェンゲゼルシャフト Formaldehyde-free aqueous binder

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63227852A (en) * 1987-03-02 1988-09-22 エア・プロダクツ・アンド・ケミカルズ・インコーポレイテツド Binder for nonwoven fabric
JPH02251656A (en) * 1989-03-16 1990-10-09 Natl Starch & Chem Corp Thermo-resistant binder for non-woven fablic not containing formaldehyde
JPH0931818A (en) * 1995-07-20 1997-02-04 Toray Ind Inc Primary backing fabric for tufted carpet, its production and tufted carpet
JP2000506940A (en) * 1996-02-21 2000-06-06 ビーエーエスエフ アクチェンゲゼルシャフト Formaldehyde-free aqueous binder
JPH10216002A (en) * 1997-02-05 1998-08-18 Unitika Ltd Primary foundation for tile carpet and manufacture thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007224493A (en) * 2007-03-29 2007-09-06 Toyobo Co Ltd Tuft carpet base fabric
JP4517305B2 (en) * 2007-03-29 2010-08-04 東洋紡績株式会社 Tuft carpet base fabric

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