JPS6037223B2 - Surface treated inorganic fiber - Google Patents

Surface treated inorganic fiber

Info

Publication number
JPS6037223B2
JPS6037223B2 JP52078787A JP7878777A JPS6037223B2 JP S6037223 B2 JPS6037223 B2 JP S6037223B2 JP 52078787 A JP52078787 A JP 52078787A JP 7878777 A JP7878777 A JP 7878777A JP S6037223 B2 JPS6037223 B2 JP S6037223B2
Authority
JP
Japan
Prior art keywords
fibers
film
fiber
treatment
titanium compound
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
JP52078787A
Other languages
Japanese (ja)
Other versions
JPS5415092A (en
Inventor
正 佐藤
繁量 草薙
次郎 伊藤
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works Ltd
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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP52078787A priority Critical patent/JPS6037223B2/en
Publication of JPS5415092A publication Critical patent/JPS5415092A/en
Publication of JPS6037223B2 publication Critical patent/JPS6037223B2/en
Expired legal-status Critical Current

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  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

【発明の詳細な説明】 本発明は表面処理無機質繊維に関するものであって、そ
の目的とするところは高強度でかつ機械的劣化の少ない
表面処理無機質繊維を提供するにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to surface-treated inorganic fibers, and its object is to provide surface-treated inorganic fibers that have high strength and less mechanical deterioration.

一般にガラスウールやロックウール等の無機質(ガラス
質)繊維は溶融紡糸後の機械的損傷がなければ非常に大
きな引張強度(200〜300k9/地)を有する。
In general, inorganic (vitreous) fibers such as glass wool and rock wool have very high tensile strength (200 to 300 k9/ground) unless mechanically damaged after melt spinning.

この機械的表面損傷を避けるために例えばガラス長繊維
に関してはサィジング剤と称して各種樹脂皮膜が繊維表
面に均一に施されている。しかしながらガラスウール、
ロックウール等の無機質短繊維は製綿時の表面処理とし
てバィンダのスプレー程度であり、繊維表面に均一な皮
膜を形成することができず、従って機械的接触によって
著しく強度が低下していた。本発明はかかる従来の欠点
を解消せんとするもので、以下詳細に説明する。
In order to avoid this mechanical surface damage, for example, with respect to long glass fibers, various resin films called sizing agents are uniformly applied to the fiber surfaces. However, glass wool
The surface treatment for inorganic short fibers such as rock wool during cotton manufacturing is limited to spraying a binder, and it is not possible to form a uniform film on the fiber surface, resulting in a significant decrease in strength due to mechanical contact. The present invention aims to overcome these conventional drawbacks and will be described in detail below.

。本発明は無機質繊維の外周にまず一般式がTi(OR
)4:〔R=C3日7,C4日9〕で表わされる有機チ
タン化合物による無定形チタン化合物の皮膜を被覆し、
更にその外周に脂肪酸ヱステルの皮膜を被覆したもので
ある。これらの皮膜の被覆処理に当っては、まず円盤法
、吹付け法等で大量に繊維化されるガラスウール、ロッ
クウール等の無機質短繊維の表面に無定形チタン化合物
の保護皮膜を均一にしかも充分な腰厚に形成せしめ、然
る後に脂肪酸ェステルの潤滑膜を更に付着又は吸着せし
めるものである。更に詳細に述べると、ガラスウール、
ロックウール等の無機質短繊維は、1300〜1500
qCの高温で溶融された鉱物原料を高速回転する円盤上
に導き、その遠心力によって円盤の周囲から繊維化する
か、或いは、ノズルから噴出された高速気流又は火炎で
吹飛ばせて繊維化する。本発明は集線時すなわち輸送用
気流によって運ばれゆるく(ルーズ)堆積された無機質
繊維をそのままの状態で(大きな外力を加えることない
こ)表面処理槽内に送入する。処理槽内に於いて有機チ
タン化合物(Ti(OR)4,R=C3日7,C4日9
)の蒸気をノズルから無機質繊維に噴出させ、更に別の
ノズルから水蒸気を同様に同時に噴出せしめる。これら
の処理蒸気と水蒸気は無機質繊維の表面近くで互いに混
合されてから繊維表面に達する。このとき繊維表面では
、有機チタン化合物が容易に加水分解縮合して無定形チ
タン化合物皮膜を繊維の全表面上に均一に形成する。こ
の方法はスプレー法による液滴の散布と異なり、気相処
理であるために繊維間の狭い空隙にも充分蒸気が到達し
て全繊維表面に皮膜を形成できる。この方法は更にCV
D(Chemical VaporDepositio
n)法と異なり、処理時間を任意に設定できるため、充
分な皮膜を得ることができる。
. In the present invention, first, the general formula is Ti(OR) on the outer periphery of the inorganic fiber.
) 4: Coating a film of an amorphous titanium compound with an organic titanium compound represented by [R = C3 day 7, C4 day 9],
Furthermore, its outer periphery is coated with a film of fatty acid ester. In coating with these films, first, a protective film of an amorphous titanium compound is uniformly applied to the surface of inorganic short fibers such as glass wool and rock wool that are made into fibers in large quantities by the disk method, spraying method, etc. It is formed to have sufficient thickness, and then a lubricating film of fatty acid ester is further attached or adsorbed. To be more specific, glass wool,
Inorganic short fibers such as rock wool have a weight of 1300 to 1500.
A mineral raw material molten at a high temperature of qC is introduced onto a disk rotating at high speed, and the centrifugal force causes it to become fibers from around the disk, or it is blown away by a high-speed air stream or flame ejected from a nozzle to form fibers. In the present invention, the loosely deposited inorganic fibers carried by the transporting air flow are fed into the surface treatment tank as they are (without applying a large external force). In the treatment tank, organic titanium compounds (Ti(OR)4, R=C3 days 7, C4 days 9
) is ejected from a nozzle onto the inorganic fibers, and water vapor is similarly ejected from another nozzle at the same time. These treatment vapors and water vapor are mixed with each other near the surface of the inorganic fiber before reaching the fiber surface. At this time, on the fiber surface, the organic titanium compound is easily hydrolyzed and condensed to uniformly form an amorphous titanium compound film on the entire surface of the fiber. Unlike the dispersion of droplets using a spray method, this method is a gas phase treatment, so that sufficient steam can reach even the narrow gaps between fibers, allowing a film to be formed on all fiber surfaces. This method further improves CV
D (Chemical Vapor Depositio)
Unlike the method n), since the treatment time can be set arbitrarily, a sufficient film can be obtained.

しかしてこの処理にあたって処理蒸気のキャリアガスと
しては乾燥空気、N2ガス等を用いる。この場合、水分
をできるだけ除去したガスを用いるが望ましい。またこ
の処理によって得られた皮膜の硬度、付着力、表面状態
は処理条件によって異なることが種々の実験から明らか
になった。即ち、表面処理雰囲気温度、処理蒸気濃度、
処理蒸気と水蒸気の濃度比〔ZO/Ti(OR)4〕、
処理蒸気の繊維間通過速度が大きな影響を及ぼすことが
明らかになった。本発明は蒸気処理を施すに当り、その
処理条件を限定するものではないが、表面処理雰囲気温
度は200℃以上が望ましい。次いで上記処理を施した
繊維に脂肪酸ヱステルの蒸気を接触させて無定形チタン
化合物皮膜上に脂肪酸ェステルの膜を形成させる。
However, in this process, dry air, N2 gas, or the like is used as a carrier gas for the process vapor. In this case, it is desirable to use a gas from which moisture has been removed as much as possible. Furthermore, various experiments have revealed that the hardness, adhesion, and surface condition of the film obtained by this treatment vary depending on the treatment conditions. That is, surface treatment atmosphere temperature, treatment vapor concentration,
Concentration ratio of treated steam and water vapor [ZO/Ti(OR)4],
It has become clear that the rate at which processing steam passes through the fibers has a significant effect. Although the present invention does not limit the treatment conditions when performing steam treatment, it is desirable that the surface treatment atmosphere temperature is 200° C. or higher. Next, the fibers subjected to the above treatment are brought into contact with fatty acid ester vapor to form a fatty acid ester film on the amorphous titanium compound film.

脂肪酸ェステルとしては炭素数が4〜24の脂肪酸のェ
ステルが望し〈、単一種類でも良く、また複数種類の混
合でもよい。処理方法は脂肪酸ェステル類を加熱するこ
とによって気化せしめ、該蒸気にチタン化合物皮膜を形
成せしめた繊維をさらすことにより、該蒸気が繊維表面
上で容易に凝縮して均一な膜を形成し得る。ここで脂肪
酸ェステルの単一又は混合膜はその下に形成されたチタ
ン化合物の有機基(一OR,R=C3日7,C74)と
のなじみが良く、付着力の強い潤滑膜を形成し得る。本
発明にあっては上述のように無機質繊維の外周に一般式
がTj(OR)4;〔R=C3日7C4日9〕で表され
る有機チタン化合物が加水分解縮合された無定形チタン
化合物の皮膜を形成してあるから、この皮膜により無機
質繊維が表面損傷から保護されて、大きな初期強度を保
持した高強度の繊維を得ることができ、しかもこのチタ
ン化合物皮膜の外周を更に脂肪酸ェステルの潤滑膜にて
被覆しているから、更に繊維同志の摩擦を軽減させて機
械的劣化が少なく高強度を長期に亘り安定して維持せし
め得る利点がある。
As the fatty acid ester, esters of fatty acids having 4 to 24 carbon atoms are desirable, and a single type or a mixture of a plurality of types may be used. In the treatment method, fatty acid esters are vaporized by heating, and by exposing the fibers on which the titanium compound film has been formed to the vapor, the vapor can easily condense on the fiber surface to form a uniform film. Here, the fatty acid ester single or mixed film has good compatibility with the organic group of the titanium compound (1OR, R=C3, C74) formed below, and can form a lubricating film with strong adhesion. . In the present invention, as described above, an amorphous titanium compound in which an organic titanium compound represented by the general formula Tj(OR)4; [R=C3day7C4day9] is hydrolyzed and condensed on the outer periphery of an inorganic fiber. This film protects the inorganic fibers from surface damage, making it possible to obtain high-strength fibers that maintain a large initial strength.Moreover, the outer periphery of this titanium compound film is further coated with fatty acid ester. Since the fibers are coated with a lubricating film, the friction between the fibers is further reduced, mechanical deterioration is small, and high strength can be stably maintained over a long period of time.

また本発明の表面処理無機質繊維を水中で分散させると
、脂肪酸ェステルの綾水性のために分散が極めて容易と
なる特長も有する。以下本発明を実施例に基づいて具体
的に説明する。
Furthermore, when the surface-treated inorganic fibers of the present invention are dispersed in water, they have the advantage that dispersion is extremely easy due to the hydrophilic nature of the fatty acid ester. The present invention will be specifically described below based on examples.

〔実施例 1〕 Si02 4仇れ%,Ca0 4仇の%、川20315
wt%,Mg0 5%からなる鉱物材料を150000
の電気炉で溶融し、該溶融材料を製綿用円盤径200側
め、回転数が300仇pm、処理量が0.4t/時間の
条件で製綿して集綿箱にルーズに堆積したウールを表面
処理槽内に挿入し、このウールに下記処理材料の黍0気
と水蒸気を別々のノズル所定の濃度比でキャリアガス(
N2)と共に同時に吹付けた。
[Example 1] Si02 4%, Ca0 4%, River 20315
150,000 wt%, mineral material consisting of Mg0 5%
The molten material was made into cotton under the conditions of a cotton-making disk with a diameter of 200 mm, a rotation speed of 300 pm, and a throughput of 0.4 t/hour, and deposited loosely in a cotton collecting box. Insert the wool into the surface treatment tank, and apply the following treatment materials, millet air and water vapor, to the wool using separate nozzles at a predetermined concentration ratio as carrier gas (
It was sprayed simultaneously with N2).

<処理条件> ・処理材料・・・テトラブトキシチタン 〔Ti(nOBu)4〕 ・処理材料蒸気濃度・・・700〜100倣Pm〃
流量・・・30ぞ/分〔キャリアガス(N2)を含む〕
・水蒸気濃度・・・700〜200皿Pm〃流量…20
夕/分〔キャリアガス (N2)を含む〕 ・処理材料蒸気温度・・・250こ○ ・水蒸気温度・・・250午0 ・処理槽内雰囲気温度・・・25000 ・処理時間・・・・・・2分 上記条件で処理した繊維を200q0に加熱したステア
リン酸ブチルの溶槽上に保ちステアリン酸ブチルの蒸気
に1分間さらしし。
<Processing conditions> - Processing material...tetrabutoxytitanium [Ti(nOBu)4] - Processing material vapor concentration...700-100 Pm
Flow rate: 30/min [including carrier gas (N2)]
・Water vapor concentration...700 to 200 plates Pm Flow rate...20
evening/minute [including carrier gas (N2)] ・Processing material steam temperature...250 pm ・Steam temperature...250 pm ・Ambient temperature inside the processing tank...25000 ・Processing time... - The fibers treated under the above conditions for 2 minutes were kept on a butyl stearate bath heated to 200q0 and exposed to butyl stearate vapor for 1 minute.

この繊維をAとする。〔実施例 2〕 実施例1と同様にテトラブトキシチタン処理を施した繊
維を14000に加熱したラゥリン酸ブチルの溶槽上に
保ち、ラウリン酸ブチルの蒸気に1分間さらした。
This fiber is called A. [Example 2] Fibers treated with tetrabutoxytitanium in the same manner as in Example 1 were kept on a butyl laurate bath heated to 14,000 ℃ and exposed to butyl laurate vapor for 1 minute.

この繊維をBとする。〔実施例 3〕 実施例1と同様にテトラブトキシチタン処理を施した繊
維を18000に加熱したャシ油の溶槽上に保ち、ャシ
油の蒸気に1分間さらした。
This fiber is called B. [Example 3] Fibers treated with tetrabutoxytitanium in the same manner as in Example 1 were kept on a chassis oil bath heated to 18,000 ℃ and exposed to chassis oil vapor for 1 minute.

この繊維をCとする。これらの実施例1〜3にて得られ
た処理繊維の引張強度の測定結果を下表に示す。
This fiber is called C. The results of measuring the tensile strength of the treated fibers obtained in Examples 1 to 3 are shown in the table below.

尚、用いた短繊維の径は10〜20ムめであった。また
機械的な強制劣化の方法は、水(常温)を2夕入れた槽
中にウールを4タ投入し、損梓翼で等速燈拝して繊維同
志を接触せしめた。然るのち、該繊維を40q○の乾燥
器中で乾燥せしめたのち引張測定に供した。但し上表中
、強度測定条件は次の通りとした。引張速度 5脚
/分スパン長さ 1仇吻 サンプル数 各40本
The diameter of the short fibers used was 10 to 20 mm. In addition, the method of mechanical forced deterioration was as follows: 4 tons of wool was placed in a tank filled with water (at room temperature) for 2 nights, and the fibers were brought into contact with each other by lighting them at a constant speed with a rotary blade. Thereafter, the fibers were dried in a 40q○ dryer and then subjected to tensile measurement. However, in the above table, the strength measurement conditions were as follows. Tensile speed: 5 legs/min Span length: 1 proboscis Number of samples: 40 each

Claims (1)

【特許請求の範囲】 1 無機質繊維の外周に一般式がTi(OR)_4;〔
R=C_3H_7,C_4H_9〕で表される有機チタ
ン化合物が加水分解縮合された無定形チタン化合物の皮
膜を被覆すると共にその外周に脂肪酸エステルの潤滑膜
を被覆して成ることを特徴とする表面処理無機質繊維。
[Claims] 1. The general formula is Ti(OR)_4 on the outer periphery of the inorganic fiber; [
R=C_3H_7, C_4H_9] is coated with a film of an amorphous titanium compound obtained by hydrolysis and condensation, and a lubricating film of fatty acid ester is coated on the outer periphery of the film. fiber.
JP52078787A 1977-06-30 1977-06-30 Surface treated inorganic fiber Expired JPS6037223B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52078787A JPS6037223B2 (en) 1977-06-30 1977-06-30 Surface treated inorganic fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52078787A JPS6037223B2 (en) 1977-06-30 1977-06-30 Surface treated inorganic fiber

Publications (2)

Publication Number Publication Date
JPS5415092A JPS5415092A (en) 1979-02-03
JPS6037223B2 true JPS6037223B2 (en) 1985-08-24

Family

ID=13671585

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52078787A Expired JPS6037223B2 (en) 1977-06-30 1977-06-30 Surface treated inorganic fiber

Country Status (1)

Country Link
JP (1) JPS6037223B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58167753U (en) * 1982-04-30 1983-11-09 日野自動車株式会社 cylinder head
JPS5996341U (en) * 1982-12-20 1984-06-29 マツダ株式会社 Engine cylinder head structure
JPS5999150U (en) * 1982-12-22 1984-07-04 マツダ株式会社 Engine cylinder head structure
JPH0830444B2 (en) * 1986-07-09 1996-03-27 本田技研工業株式会社 Engine cylinder head
GB2232997B (en) * 1989-06-05 1993-07-21 Sanyo Chemical Ind Ltd Textile treating compositions
US5269950A (en) * 1989-06-05 1993-12-14 Sanyo Chemical Industries, Ltd. Textile treating compositions

Also Published As

Publication number Publication date
JPS5415092A (en) 1979-02-03

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