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JPS5951627B2 - Surface treatment method for inorganic fibers - Google Patents
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JPS5951627B2 - Surface treatment method for inorganic fibers - Google Patents

Surface treatment method for inorganic fibers

Info

Publication number
JPS5951627B2
JPS5951627B2 JP52125353A JP12535377A JPS5951627B2 JP S5951627 B2 JPS5951627 B2 JP S5951627B2 JP 52125353 A JP52125353 A JP 52125353A JP 12535377 A JP12535377 A JP 12535377A JP S5951627 B2 JPS5951627 B2 JP S5951627B2
Authority
JP
Japan
Prior art keywords
surface treatment
wool
fibers
treatment agent
adsorbent
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
JP52125353A
Other languages
Japanese (ja)
Other versions
JPS5459496A (en
Inventor
正 佐藤
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 JP52125353A priority Critical patent/JPS5951627B2/en
Publication of JPS5459496A publication Critical patent/JPS5459496A/en
Publication of JPS5951627B2 publication Critical patent/JPS5951627B2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B20/00Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
    • C04B20/10Coating or impregnating
    • C04B20/1018Coating or impregnating with organic materials
    • C04B20/1022Non-macromolecular compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • 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】 本発明は無機質繊維に有機金属表面処理剤を吸着せしめ
た吸着材および水を吸着せしめた吸着材を混合し、次い
で加熱して有機金属表面処理剤および水を気化させると
共に気化した有機金属表面処理剤と水蒸気を接触させて
無機質繊維表面に有機金属化合物皮膜を形成することを
特徴とする無機質繊維の表面処理法に関するものであり
、その目的とするところは機械的または化学的な劣化の
少ない高強度の無機質繊維を得ることができる無機質繊
維の表面処理法を提供することにある。
Detailed Description of the Invention The present invention involves mixing an adsorbent in which an organic metal surface treatment agent is adsorbed onto inorganic fibers and an adsorption material in which water is adsorbed, and then heating the mixture to vaporize the organic metal surface treatment agent and water. The present invention relates to a surface treatment method for inorganic fibers, which is characterized by forming an organic metal compound film on the surface of inorganic fibers by bringing the vaporized organic metal surface treatment agent into contact with water vapor. It is an object of the present invention to provide a method for surface treatment of inorganic fibers that can obtain high-strength inorganic fibers with little chemical deterioration.

無機質繊維は紡糸直後は非常に大きな引張強度(200
〜300kg/m4)を有するが取扱中に損傷し易いの
で従来から無機質繊維の機械的または化学的な表面の損
傷を防止するため各種の表面処理方法が検討されている
が、ガラスウール、ロックウール等の無機質短繊維の表
面に均一な皮膜を形成できる表面処理法は未だに開発さ
れておらず、無機質短繊維の強度は極めて低いものにな
ってしまう。
Immediately after spinning, inorganic fibers have a very high tensile strength (200
~300kg/m4), but they are easily damaged during handling.Therefore, various surface treatment methods have been considered to prevent mechanical or chemical damage to the surface of inorganic fibers, including glass wool, rock wool, etc. A surface treatment method capable of forming a uniform film on the surface of inorganic short fibers has not yet been developed, and the strength of the inorganic short fibers becomes extremely low.

本発明はかかる欠点を解消するものであって、以下詳細
に説明する。
The present invention solves these drawbacks and will be described in detail below.

ガラスウール、ロックウール等の無機質短繊維は通常1
300〜1500℃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
ら繊維化するかあるいは溶融された原料をノズルから流
出させ高速気流または火炎で溶融体を吹き飛ばして繊維
化し、これらの繊維は輸送用気流によって集綿箱に送ら
れ、次いでコンベアーに集積されて搬送される。
Inorganic short fibers such as glass wool and rock wool are usually 1
Mineral raw materials melted at a high temperature of 300 to 1500 degrees Celsius are introduced onto a disk rotating at high speed, and the centrifugal force is used to turn them into fibers from around the disk, or the molten raw materials are flowed out of a nozzle and the molten material is blown out with a high-speed air stream or flame. The fibers are blown into fibers and transported by a transport air stream to a collection box, then collected and conveyed on a conveyor.

本発明の表面処理法は例えばこのコンベアー上にルーズ
に集積され搬送中の短繊維に表面処理剤を吸着せしめた
吸着材および水を吸着せしめた吸着材を散布して混入せ
しめ、しかるのち表面処理槽に導びいて100〜350
℃に加熱することによって行なわれる。
In the surface treatment method of the present invention, for example, short fibers that are loosely accumulated on this conveyor and being transported are mixed with an adsorbent in which a surface treatment agent is adsorbed and an adsorbent in which water is adsorbed, and then the surface treatment is carried out. 100-350 when led to the tank
This is done by heating to ℃.

表面処理剤としては例えばTi(OR)4 (但しRは
C4H9,C3H7,C2H5などのアルキル基を示す
)で示される有機チタン化合物、Zr(OR)4 〔但
しRはC4H9,C3H7,C2H5などのアルキル基
を示す〕で示さる有機ジルコン化合物などの有機金属化
合物などが用いられる。
Examples of surface treatment agents include organic titanium compounds represented by Ti(OR)4 (where R represents an alkyl group such as C4H9, C3H7, C2H5, etc.) and Zr(OR)4 [wherein R represents an alkyl group such as C4H9, C3H7, C2H5, etc.]. Organometallic compounds such as organic zircon compounds represented by [indicating an alkyl group] are used.

また表面処理剤乃至水の吸着材としてはフラースアース
、活性白土、ボーキサイト、木炭、活性炭、骨炭、モレ
キュラーシーブ、シリカゲル、ベントナイト、マグネシ
ア、賦活アルミナ、無機質バルーン(例えば゛シラスバ
ルーン)などか゛用いられる。
Further, as the surface treatment agent or water adsorbent, there are used, for example, fuller's earth, activated clay, bauxite, charcoal, activated carbon, bone charcoal, molecular sieve, silica gel, bentonite, magnesia, activated alumina, and inorganic balloons (for example, Shirasu balloon).

加熱温度は表面処理剤の種類によっても異なるが一般に
100〜350℃であり、水および表面処理剤を蒸発さ
せることができる温度であればよく最低100℃であり
、あまり高い温度にす5ると熱損失が大きくなると共に
処理された繊維に好ましくない影響を与えることがある
The heating temperature varies depending on the type of surface treatment agent, but is generally 100 to 350℃, and should be at least 100℃ as long as it can evaporate water and the surface treatment agent. Heat losses are high and can have an undesirable effect on the treated fibers.

尚、表面処理した繊維から吸着材を分離して再使用に供
することができるが、繊維に吸着材を混合したままで用
いることもできる。
Although the adsorbent can be separated from the surface-treated fibers and reused, it is also possible to use the adsorbent mixed with the fibers.

而して本発明において無機質短繊維に表面処理剤を吸着
せしめた吸着材および水を吸着せしめた吸着材を混合し
たのち、直ちに100〜350℃に加熱すると表面処理
剤および水は気化して吸着材から脱着すると共に気化し
た表面処理剤蒸気および水蒸気は短繊維の近傍で接触し
、表面処理剤は水蒸気によって加水分解して縮合し無定
形の有機金属化合物皮膜を短繊維の全表面に均一に形成
する。
Therefore, in the present invention, when the adsorbent in which the surface treatment agent is adsorbed to inorganic short fibers and the adsorbent in which water is adsorbed are mixed and immediately heated to 100 to 350°C, the surface treatment agent and water are vaporized and adsorbed. The surface treatment agent vapor and water vapor that are vaporized as they are desorbed from the material come into contact near the short fibers, and the surface treatment agent is hydrolyzed and condensed by the water vapor, forming an amorphous organometallic compound film uniformly over the entire surface of the short fibers. Form.

このように表面処理が気相処理であるため短繊維間の空
隙に表面処理剤蒸気および水蒸気が充分に拡散、浸透し
全繊維表面に斑なく均一に被膜を形成でき、しかも表面
処理剤および水は吸着材に吸着されているので繊維の極
く近傍で気化して繊維に供給されるので極めて効率良く
処理することができる。
Since the surface treatment is a vapor phase treatment, the surface treatment agent vapor and water vapor can sufficiently diffuse and penetrate into the voids between the short fibers, forming a uniform coating on the entire fiber surface. Since it is adsorbed by the adsorbent, it is vaporized very close to the fibers and supplied to the fibers, so it can be processed extremely efficiently.

表面処理剤である有機金属化合物は水分に対して非常に
敏感であり水分と接触すると即座に加水分解を起こすの
で表面処理剤を気相状態で処理装置まで輸送することは
技術的に困難であるしたとえ不可能でないにしても輸送
効率が低下し、また表面処理剤を単独で液相状態で輸送
して使用する場合は特別な輸送装置あるいは気化装置が
必要となるためコスト高になるが、吸着材に吸着させる
と輸送、取扱いなどが極めて容易にできしかも気化のた
めの特別な装置を必要としないものである。
The organometallic compound used as a surface treatment agent is extremely sensitive to moisture and immediately undergoes hydrolysis when it comes into contact with moisture, so it is technically difficult to transport the surface treatment agent in a gaseous state to the treatment equipment. However, even if it is not impossible, the transportation efficiency will be reduced, and if the surface treatment agent is transported alone in a liquid phase and used, special transportation equipment or vaporization equipment will be required, which will increase the cost. When adsorbed onto an adsorbent, transportation and handling are extremely easy, and special equipment for vaporization is not required.

本発明によって得られた繊維は充填材、吸音材、断熱材
などとして好ましく使用することができる。
The fibers obtained according to the present invention can be preferably used as fillers, sound absorbing materials, heat insulating materials, and the like.

尚、上記の説明においては主として無機質短繊維の表面
処理について述べたが本発明は勿論無機質長繊維にも適
用できるものである。
In the above description, the surface treatment of inorganic short fibers was mainly described, but the present invention is of course applicable to inorganic long fibers.

本発明にあっては無機質繊維に有機金属表面処理剤を吸
着せしめた吸着材および水を吸着せしめた吸着材を混合
したので、無機質繊維の極く近傍で表面処理剤および水
を気化することができ極めて効率の良い表面処理をする
ことができしかも表面処理装置へ容易に輸送できると共
に取扱いが極めて容易であって安価なコストで処理でき
るものであり、しかも加熱して有機金属表面処理剤およ
び水を気化させると共に気化した有機金属表面処理剤と
水蒸気を接触させて無機質繊維に有機金属化合物皮膜を
形成させるので無機質繊維間の空隙に気化した表面処理
剤および水蒸気が均一に拡散し全繊維表面に均一に有機
金属化合物皮膜を形成することができ、引張強度の大な
る繊維を得ることか゛できるものである。
In the present invention, since an adsorbent in which an organic metal surface treatment agent is adsorbed and an adsorbent in which water is adsorbed are mixed with inorganic fibers, the surface treatment agent and water can be vaporized very close to the inorganic fibers. It can perform extremely efficient surface treatment, can be easily transported to surface treatment equipment, is extremely easy to handle, can be processed at low cost, and can be heated to produce organometallic surface treatment agents and water. At the same time, the vaporized organic metal surface treatment agent is brought into contact with water vapor to form an organic metal compound film on the inorganic fibers, so the vaporized surface treatment agent and water vapor are uniformly diffused into the voids between the inorganic fibers, covering the entire fiber surface. It is possible to form a uniform organometallic compound film and to obtain fibers with high tensile strength.

以下実施例により本発明を具体的に説明する。The present invention will be specifically explained below using Examples.

尚%は全て重量%を示す。All percentages are by weight.

〈無機質短繊維の製造〉 下記組成の材料を溶融し、直径200mmの製綿用円盤
を300Orpmで回転させて遠心力によって繊維化し
Q、2t/hrで無機質短繊維(ウール)を得た。
<Production of inorganic short fibers> Materials having the following composition were melted, and a cotton-making disk with a diameter of 200 mm was rotated at 300 rpm to form fibers by centrifugal force to obtain inorganic short fibers (wool) at Q, 2 t/hr.

材料組成 5iOz CaOA40s Mg040%
40% 15% 5% 〈実施例 1〉 テトラブトキシチタン〔Ti(OC4H9)4〕の中に
活性炭の粉末を浸漬し、即座に濾過して得たテトラブト
キシチタン吸着活性炭をウール重量に対して2%および
水中ににシラスバルーンを1時間浸漬して得た吸水シラ
スバルーンをウール重量に対して5%をそれぞれ上記ウ
ールに散布混合した。
Material composition 5iOz CaOA40s Mg040%
40% 15% 5% <Example 1> Activated carbon powder was immersed in tetrabutoxytitanium [Ti(OC4H9)4] and immediately filtered to obtain tetrabutoxytitanium-adsorbing activated carbon at a ratio of 2% to the weight of wool. % and water-absorbing shirasu balloons obtained by immersing the shirasu balloons in water for 1 hour, in an amount of 5% based on the weight of the wool, were sprinkled and mixed on the wool.

然るのち200℃の表面処理槽内に2分間保ち処理を完
了した。
Thereafter, it was kept in a surface treatment tank at 200° C. for 2 minutes to complete the treatment.

ウールの繊維直径は9〜15μ、繊維表面の無定形チタ
ン化合物の平均膜厚は200人であった。
The fiber diameter of the wool was 9 to 15 μm, and the average film thickness of the amorphous titanium compound on the fiber surface was 200 μm.

上記処理を行なったウール及び未処理ウールの引張強度
を測定した結果は次のとおりであった。
The results of measuring the tensile strength of the wool subjected to the above treatment and the untreated wool were as follows.

未処理ウール 105kg/i4
処理ウール 183kg/m4
引張強度測定条件: ウール長 10mm引
張速度 5 mm/minm
/m用数 各40本本処理ウ
ールの使用に当っては吸着材を分離除去する必要性は全
くなかった。
Untreated wool 105kg/i4
Treated wool 183kg/m4
Tensile strength measurement conditions: Wool length 10mm Tensile speed 5mm/minm
/m Number of uses: 40 each When using this treated wool, there was no need to separate and remove the adsorbent.

〈実施例 2〉 テトラブトキシジルコン〔Zr(OC4H9)4〕の中
に活性白土の粉末を浸漬し即座に濾過して得たテトラブ
トキシジルコン吸着白土をウールに対して1.5%およ
び吸湿したシリカゲルをウールに対して4%をそれぞれ
上記ウールに散布混合した。
<Example 2> Tetrabutoxyzircon adsorbed clay obtained by immersing activated clay powder in tetrabutoxyzircon [Zr(OC4H9)4] and immediately filtering it was mixed with 1.5% of tetrabutoxyzircon based on wool and silica gel that had absorbed moisture. The above-mentioned wool was sprayed and mixed in an amount of 4% based on the wool.

然るのち、280℃の表面処理槽内に3分間保ち処理を
完了した。
Thereafter, it was kept in a surface treatment tank at 280° C. for 3 minutes to complete the treatment.

ウールの繊維直径は9〜15μ、繊維表面の無定形ジル
コン化合物の平均膜厚は110人で゛あった。
The fiber diameter of the wool was 9 to 15 μm, and the average thickness of the amorphous zircon compound on the fiber surface was 110 μm.

上記処理を行なったウール及び未処理ウールを下記のセ
メントアルカリ溶液中に浸漬したのちそれぞれの引張強
度を測定した結果は次のとおりであった。
The treated wool and untreated wool were immersed in the cement alkaline solution described below, and the tensile strength of each was measured, and the results were as follows.

セメントアルカリ溶液に浸漬前の引張強度:未処理ウー
ル 110kg/7rtIl処理
ウール 180kg/m1−k
17)7/L/力゛ノ NaOHKOHCa(OH)2
溶液の組成 (PH= 12.6 ) o、s8.?/n 3.4
5g/lo、489/l。
Tensile strength before immersion in cement alkaline solution: untreated wool 110 kg/7rtIl treated wool 180 kg/m1-k
17) 7/L/force ゛no NaOHKOHCa(OH)2
Composition of solution (PH=12.6) o, s8. ? /n 3.4
5g/lo, 489/l.

〈実施例 3〉 テ1〜ラフ斗キシチタンの中に活性炭の粉末を浸漬し即
座に濾過して得たテ1へラフ斗キシチタン吸着活性炭を
ウールに対して1%、 テトラフ用・キシジルコンの中にフラースアースを浸漬
し、即座に濾過して得たフラースアースをウールに対し
て1%および 水中にシラスバルーンを1時間浸漬して得た吸水シラス
バルーンをウールに対して5%をギれぞれウールに散布
混合した。
〈Example 3〉 Activated carbon powder was immersed in tetraph titanium and immediately filtered. Activated carbon adsorbed on tetraph oxidized titanium was added at 1% to wool, and activated carbon was soaked in tetraph oxidizircon. Fuller's earth is soaked and immediately filtered to give 1% of the wool, and water-absorbing shirasu balloons obtained by soaking the shirasu balloon in water for 1 hour are added to the wool at 5%. Sprayed and mixed on wool.

然るのち、250℃の表面処理槽内に2m1n間保ち、
処理を完了した。
After that, it was kept in a surface treatment tank at 250°C for 2m1n,
Processing completed.

繊維表面には、チタン化合物、ジルコン化合物の無定形
混合被膜が形成され、その平均膜厚は200人で゛あっ
た。
An amorphous mixed film of a titanium compound and a zircon compound was formed on the fiber surface, and the average film thickness was 200 mm.

上記処理を行なったウールは実施例1及び実施例2と同
様な性質を有し本処理ウールを充填材として使用するに
当っては吸着材を分離除去する必要性は全くなかった。
The wool treated as described above had properties similar to those of Examples 1 and 2, and there was no need to separate and remove the adsorbent when using this treated wool as a filler.

Claims (1)

【特許請求の範囲】[Claims] 1 無機質繊維に有機金属表面処理剤を吸着せしめた吸
着材および水を吸着せしめた吸着材を混合し、次いで加
熱して有機金属表面処理剤および水を気化させると共に
気化した有機金属表面処理剤と水蒸気を接触させて無機
質繊維表面に有機金属化合物皮膜を形成することを特徴
とする無機質繊維の表面処理法。
1. Mix an adsorbent in which an organic metal surface treatment agent is adsorbed to an inorganic fiber and an adsorbent in which water is adsorbed, and then heat to vaporize the organic metal surface treatment agent and water, and combine the vaporized organic metal surface treatment agent with the adsorbent. A method for surface treatment of inorganic fibers, which comprises forming an organic metal compound film on the surface of the inorganic fibers by contacting them with water vapor.
JP52125353A 1977-10-15 1977-10-15 Surface treatment method for inorganic fibers Expired JPS5951627B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52125353A JPS5951627B2 (en) 1977-10-15 1977-10-15 Surface treatment method for inorganic fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52125353A JPS5951627B2 (en) 1977-10-15 1977-10-15 Surface treatment method for inorganic fibers

Publications (2)

Publication Number Publication Date
JPS5459496A JPS5459496A (en) 1979-05-14
JPS5951627B2 true JPS5951627B2 (en) 1984-12-14

Family

ID=14908017

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52125353A Expired JPS5951627B2 (en) 1977-10-15 1977-10-15 Surface treatment method for inorganic fibers

Country Status (1)

Country Link
JP (1) JPS5951627B2 (en)

Also Published As

Publication number Publication date
JPS5459496A (en) 1979-05-14

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