JPH01304018A - Preparation of filter material - Google Patents

Preparation of filter material

Info

Publication number
JPH01304018A
JPH01304018A JP13315788A JP13315788A JPH01304018A JP H01304018 A JPH01304018 A JP H01304018A JP 13315788 A JP13315788 A JP 13315788A JP 13315788 A JP13315788 A JP 13315788A JP H01304018 A JPH01304018 A JP H01304018A
Authority
JP
Japan
Prior art keywords
filter material
water
cellulose
spun yarn
nonwoven fabric
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP13315788A
Other languages
Japanese (ja)
Other versions
JPH0416207B2 (en
Inventor
Yoshimitsu Nakajima
中島 祥光
Tadashi Suzuki
正 鈴木
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.)
Takano Corp
Original Assignee
Takano 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 Takano Corp filed Critical Takano Corp
Priority to JP13315788A priority Critical patent/JPH01304018A/en
Publication of JPH01304018A publication Critical patent/JPH01304018A/en
Publication of JPH0416207B2 publication Critical patent/JPH0416207B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Filtering Materials (AREA)
  • Artificial Filaments (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)

Abstract

PURPOSE:To prepare an inexpensive filter material according to a mass production system, by forming an activated fiber having a bilateral structure based on a methylol derivative of a cellulose xanthate into spun yarn and heat-treating said spun yarn along with water. CONSTITUTION:An activated fiber having a bilateral structure based on a methylol derivative of cellulose xanthate is formed into spun yarn which is, in turn, heat-treated along with water to prepare a filter material. By this method, the activated fiber developed by a no-binder cellulose nonwoven fabric manufacturing process of a pons-bonding system due to a TCF (Te X tile Continuously Formed) method is improved as one for a filter material and the mass production of the inexpensive filter material can be achieved by consistent production from a raw material to the material while bulkiness is held as it is without losing the water and safety as the filter material possessed by the nonwoven fabric.

Description

【発明の詳細な説明】 [産業上の利用分野コ 本発明は、オイル等に混入する夾雑物を濾過するための
濾過素材の製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing a filter material for filtering impurities mixed in oil or the like.

[従来の技術] 濾過素材としてセルロース繊維を用いると、このセルロ
ース繊維は通常の状態では熱可塑性はなく水素結合によ
る自着性も極めて弱いために、湿潤時にその水素結合が
切れ1紙のように膨張・分解する欠点がある。しかし、
一方でこのセルロース繊維は親水性、吸水性に優れ、熱
安定性、安全性等を有する長所もある。
[Prior art] When cellulose fiber is used as a filter material, the cellulose fiber is not thermoplastic in its normal state and has very weak self-adhesion due to hydrogen bonds, so when it gets wet, the hydrogen bonds break and it becomes like a piece of paper. It has the disadvantage of expanding and decomposing. but,
On the other hand, this cellulose fiber has excellent hydrophilicity and water absorption, and also has advantages such as thermal stability and safety.

一方、不織布は応用分野の拡大展開時に、ta維の交絡
法、バインダ等が研究開発され、多面的な進歩をもたら
されたが、セルロース繊維が木来持っている親木性・吸
水性・熱安定性及び安全性を犠牲にして作られているセ
ルロース不織布の場合が多い、しかし、僅かながら、ノ
ーバインダセルロースとしてビスコースから繊維化に至
る過程で、水素結合と強化交絡法によるもの及び活性化
繊維の持つ特性を巧みに生かしたTCF(Textil
e Continuously Foraied)法に
よる100%再生セルロースが知られている。この中間
体繊維であるTCP活性化Fa雄は、ビスコースをメチ
ロール化剤を含有する紡糸浴中に紡出することによって
形成される。
On the other hand, when non-woven fabrics were expanded in the field of application, research and development of methods for interlacing TA fibers, binders, etc. brought about multifaceted progress. In many cases, cellulose nonwoven fabrics are made at the expense of thermal stability and safety.However, in the process from viscose to fiberization as binderless cellulose, there are some that are made using hydrogen bonding and reinforced entangling methods and active TCF (Textil), which skillfully takes advantage of the properties of synthetic fibers,
100% regenerated cellulose produced by the Continuously Foraid method is known. This intermediate fiber, TCP-activated Fa male, is formed by spinning viscose into a spinning bath containing a methylolating agent.

TCP活性化u&維は、ハイドロキン・メチルφセルロ
ース拳ザンテート(以下HMCXと称する)を主成分と
するメチルオール化誘導体のセルロース・ザンテートで
ある。HMCXはビスコース紡糸段階で、第1図に示す
ようにセルロース1、HMCX2、及ヒソジューム・セ
ルロース・ザンテート(以下NaCXと称する)3が、
同心円的に分布した三相構造を形成している。この状態
の繊維を延伸操作を行うことにより、第2図に示すよう
なパイラテラル構造のTCP活性化繊維が得られる。
TCP-activated u&fiber is cellulose xanthate, a methylolated derivative whose main component is hydroquine methyl φ cellulose xanthate (hereinafter referred to as HMCX). HMCX is a viscose spinning stage, and as shown in Figure 1, cellulose 1, HMCX 2, and hisodium cellulose xanthate (hereinafter referred to as NaCX) 3 are
It forms a three-phase structure distributed concentrically. By drawing the fiber in this state, a TCP-activated fiber having a pilateral structure as shown in FIG. 2 can be obtained.

このTCP活性化1m、!iが示す特長的性質は、それ
ぞれの構成物質によって発揮され、1(MCX2は収縮
性、捲縮性を発揮して素材の持つ多様な繊維間隔の保持
を有利にし、セルロース1は機械的強度を保持する骨格
的構造材となり、更にNaCX3は強親水性の成分とし
て吸水性を発揮することになる。
This TCP activation 1m! The characteristic properties exhibited by i are exhibited by each constituent material. NaCX3 serves as a skeletal structural material to hold the water, and also exhibits water absorbing properties as a strongly hydrophilic component.

不織布はこの活性化繊維を水に分散し、ウェブを形成、
熱圧着して造られている。この不織布を濾過素材に使用
するには、例えば−旦細条状に裁断してから紐状に撚る
ことにより行われている。
Nonwoven fabrics are made by dispersing these activated fibers in water to form a web.
It is made by heat pressing. In order to use this nonwoven fabric as a filter material, for example, it is first cut into strips and then twisted into strings.

しかし、このような手段による濾過素材の製造は、工程
が増加する問題点がある。
However, manufacturing a filtration material by such means has the problem of increasing the number of steps.

[発明の目的] 本発明の目的は、上述の問題点を解消し、活性化繊維か
ら直接製造し、活性化mixが有する液体濾過特性を十
分に生かし、しかも多量かつ安価に供給し得る濾過素材
の製造方法を提供することにある。
[Object of the Invention] The object of the present invention is to solve the above-mentioned problems, to provide a filtration material that can be produced directly from activated fibers, fully utilizes the liquid filtration properties of the activated mix, and can be supplied in large quantities and at low cost. The purpose of this invention is to provide a method for manufacturing the same.

[発明の概要] 上述の目的を達成するための本発明の要旨は。[Summary of the invention] The gist of the present invention is to achieve the above objects.

セルロースザンテートのメチロール化誘導体を主成分と
するパイチラル構造を持つ活性化繊維を紡糸に形成し、
該紡糸を水と共に加熱処理して濾過素材を製造すること
を特徴とする濾過素材の製造方法である。
Activated fibers with a pithral structure mainly composed of a methylolated derivative of cellulose xanthate are formed by spinning,
This is a method for producing a filter material, characterized in that the spun yarn is heat-treated with water to produce a filter material.

[発明の実施例] この濾過素材の製造は、上述のTCP活性化繊維を次の
工程を経てなされる。   ゛(1)集合紡糸すること
により1毛糸状の紡糸を形成する。
[Embodiments of the Invention] This filtration material is manufactured by using the above-mentioned TCP activated fibers through the following steps. (1) One yarn-like yarn is formed by collective spinning.

(2)水と共に加熱処理により収縮性及び巻縮性を発現
させ紡糸のバルキ性を付加して、活性状態から熱可塑性
のない安定した再生セルロースに軟化し、糸の構造を確
立する。
(2) Heat treatment with water develops shrinkage and crimpability to add bulkiness for spinning, softening the active state to stable regenerated cellulose without thermoplasticity and establishing the structure of the yarn.

(3)不純物を精錬で除去し乾燥しする。(3) Remove impurities by smelting and drying.

HMCXは水と共に熱を加えると、粘稠状態となり接触
繊維間で拡散が生ずると共に、HMCX成分がセルロー
スに転化し、更に熱可塑性を失い水素結合により強固な
融着を起こす、また。
When HMCX is heated with water, it becomes viscous and diffusion occurs between the contacting fibers, and the HMCX component is converted to cellulose, which further loses its thermoplasticity and causes strong fusion due to hydrogen bonding.

HMCX成分がセルロースに転化する間にその収縮性、
捲縮性を発現し、収縮力は約10秒で最大に達し、最大
収縮力は約13 mg/dである。このように転化し終
った繊維は波状の捲縮した繊維となり、その断面はパイ
ラテラル状の形態を有し、濾過特性に示す微細な夾雑物
までの除去能力と他に類を見ない保水性を有することに
なる。
the shrinkage properties of the HMCX component during its conversion to cellulose;
It exhibits crimpability, and the contractile force reaches its maximum in about 10 seconds, and the maximum contractile force is about 13 mg/d. The fibers that have been converted in this way become wavy, crimped fibers that have a pilateral cross-section, and have the ability to remove even the finest impurities as shown in their filtration properties, as well as unparalleled water retention. will have the following.

このように製造された濾過素材の実際の使用にちっては
、オイル濾過器などに適用することが好適である。オイ
ル濾過器においては、例えばパンチングメタルなどの多
数の小孔を有する金属製の内部円筒の岡囲にいおのI!
!過素材を巻き付け、その外方を円筒状金属管から成る
外部円筒で囲んだ構造とする。そして、オイルを内部円
筒と外部円筒の間に注ぎ込むと、内部円筒に巻かれた濾
過素材を通過する際に、オイル中の夾雑物が濾過される
ことになる。11!過素材を内部円筒に密度勾配を有す
るハネカム状に巻き付ければ、それによって得られる多
様式通路と大表面化に加え1毛糸状紡糸の持つ多様な細
孔間隔と繊維の持つ微小濾孔との組み合わせにより、極
めて大量でしかも多様な濾過が行われる。
Regarding the actual use of the filter material manufactured in this way, it is suitable to apply it to an oil filter or the like. In an oil filter, an inner cylinder made of metal such as punched metal with a large number of small holes is surrounded by an inner cylinder.
! It has a structure in which the outer material is wrapped around it and the outer side is surrounded by an outer cylinder made of a cylindrical metal tube. Then, when oil is poured between the inner cylinder and the outer cylinder, impurities in the oil are filtered out as it passes through the filter material wrapped around the inner cylinder. 11! By wrapping the filter material around the inner cylinder in a honeycomb shape with a density gradient, in addition to the various passageways and large surface area obtained, a combination of the various pore spacings of yarn-like spinning and the microscopic pores of fibers can be obtained. This allows extremely large and diverse filtration to be carried out.

[発明の効果1 以上説明したように本発明に係る濾過素材の製造方法は
TCF法によるスパンポンド方式のノーバインダセルロ
ース不織布の製造工程により開発された活性化tJj!
を濾過素材用に改良し、しかも不織布が持つ濾過素材と
しての吸水性、熱安定性、安全性を損することなく、ま
たバルキ性をもそのまま保持しながら、原料から素材ま
でを一貫生産することにより安価な濾過素材が得られる
[Effect of the Invention 1 As explained above, the method for manufacturing the filtration material according to the present invention is an activated tJj!
By improving the nonwoven fabric for use as a filtration material, and without sacrificing the water absorption, thermal stability, and safety properties of nonwoven fabric as a filtration material, and while maintaining the same bulk properties, we have integrated production from raw materials to materials. An inexpensive filtration material can be obtained.

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

図面第1図はビスコース紡糸段階におけるセルロースの
断面図、第2図はバイテラル構造の活性化不織布の断面
図である。 特許出願人   株 式 会 社 高 野第1図 第2図
Figure 1 is a cross-sectional view of cellulose at the viscose spinning stage, and Figure 2 is a cross-sectional view of an activated nonwoven fabric with a biteral structure. Patent applicant Takano Co., Ltd. Figure 1 Figure 2

Claims (1)

【特許請求の範囲】[Claims] 1、セルロースザンテートのメチロール化誘導体を主成
分とするバイテラル構造を持つ活性化繊維を紡糸に形成
し、該紡糸を水と共に加熱処理して濾過素材を製造する
ことを特徴とする濾過素材の製造方法。
1. Production of a filtration material characterized by forming activated fibers with a biteral structure mainly composed of a methylolated derivative of cellulose xanthate into a spun fiber, and heat-treating the spun fiber with water to produce a filtration material. Method.
JP13315788A 1988-05-31 1988-05-31 Preparation of filter material Granted JPH01304018A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13315788A JPH01304018A (en) 1988-05-31 1988-05-31 Preparation of filter material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13315788A JPH01304018A (en) 1988-05-31 1988-05-31 Preparation of filter material

Publications (2)

Publication Number Publication Date
JPH01304018A true JPH01304018A (en) 1989-12-07
JPH0416207B2 JPH0416207B2 (en) 1992-03-23

Family

ID=15098029

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13315788A Granted JPH01304018A (en) 1988-05-31 1988-05-31 Preparation of filter material

Country Status (1)

Country Link
JP (1) JPH01304018A (en)

Also Published As

Publication number Publication date
JPH0416207B2 (en) 1992-03-23

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