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JPS6149438B2 - - Google Patents
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JPS6149438B2 - - Google Patents

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Publication number
JPS6149438B2
JPS6149438B2 JP52085507A JP8550777A JPS6149438B2 JP S6149438 B2 JPS6149438 B2 JP S6149438B2 JP 52085507 A JP52085507 A JP 52085507A JP 8550777 A JP8550777 A JP 8550777A JP S6149438 B2 JPS6149438 B2 JP S6149438B2
Authority
JP
Japan
Prior art keywords
fibrous
starch
moisture absorption
plate
polyhydric alcohol
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
JP52085507A
Other languages
Japanese (ja)
Other versions
JPS5420068A (en
Inventor
Takashi Takiuchi
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 JP8550777A priority Critical patent/JPS5420068A/en
Publication of JPS5420068A publication Critical patent/JPS5420068A/en
Publication of JPS6149438B2 publication Critical patent/JPS6149438B2/ja
Granted legal-status Critical Current

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  • Paper (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は繊維質板状体の製造方法に関するも
のである。 従来、繊維質板状体は、ロツクウール、ガラス
ウール等の繊維質材料をでんぷん結合剤によつて
結合させて製造していた。ところが、でんぷんは
吸湿性が高く、かつ吸湿状態のでんぷんは弾性率
が低下するため、吸湿した繊維質板状体は変形し
やすかつた。これを解消するため、第1の方法と
してでんぷん結合剤に代えて他の結合剤を用いた
り、でんぷんと他の結合剤を併用する方法が提案
された。この場合、他の結合剤としては、例えば
アクリル樹脂、酢酸ビニル樹脂等のエマルジヨン
またはメラミン樹脂、エポキシ樹脂、ユリア樹
脂、フエノール樹脂等が用いられる。第2の方法
として、でんぷんを結合剤とした板状体の表面
に、上記の他の結合剤を塗装して吸湿による変形
を防止する方法が提案された。しかしながら、こ
れらの方法は、つぎのような欠点があつた。すな
わち、(1)吸湿変形防止効果が小さい場合がある。
(2)吸湿変形防止効果を高めるにはコストが高くな
る。(3)第2の方法では製造工程が複雑になる。 したがつて、この発明の目的は、そのような欠
点のない繊維質板状体の製造方法を提供すること
である。 この発明の特徴は、エチレングリコール、プロ
ピレングリコール、ブタンジオール、ペンタンジ
オール、グリセリン、ペンタエリスリトール、ポ
リエチレングリコールおよびポリプロピレングリ
コールよりなる群から選ばれた分子量1000以下の
多価アルコールと、でんぷんと、繊維質材料と、
水との混合物からウエツトマツトをつくり、この
ウエツトマツトを乾燥させることを特徴とする繊
維質板状体の製造方法にある。 つぎに、この発明を詳しく説明する。 この発明で用いる繊維質材料としては、例えば
ロツクウール、ガラスウール、アスベスト、パル
プ等があげられる。 低分子量の多価アルコールとしては、エチレン
グリコール、プロピレングリコール、ブタンジオ
ール、ペンタンジオール、グリセリン、ペンタエ
リスリトール、ポリエチレングリコール、ポリプ
ロピレングリコール等が用いられる。それらの分
子量は1000以下が好ましい。そのようなものは、
水に可溶で、でんぷんと相溶性があり、比較的安
価である。そして、繊維質板状体製造中に、でん
ぷんや繊維質材料と反応したり、それ自身変質し
たりすることなく、また製造中に揮発しにくいと
いう性質をもつ。このような多価アルコールの混
合量は、でんぷんに対し重量基準で3〜60%が適
当であり、望ましくは5〜30%である。3%以下
では効果が少なく、また60%以上では結合剤とし
て常態での特性、例えば強度の低下がおこり望ま
しくない。 でんぷん結合剤に、このような多価アルコール
を加えることにより繊維質板状体の耐湿性が向上
する理由は、つぎのように考えられる。すなわ
ち、通常、繊維質板状体は、配合物と水の混合液
から5〜20mmの厚さのウエツトな板をつくり、こ
れを乾燥することにより製造されるが、結合剤と
してのでんぷんは、この間に糊化し乾燥されて固
化していく。乾燥工程では、はじめの中は恒率乾
燥で板全体から均一に水分が減少するが、減率乾
燥に移ると板表面に近い部分は中央部分に比べ早
く水分が失なわれていく。その結果、板表面は収
縮する傾向になり引張応力が作用する。更に乾燥
がすすむと、逆に内部に引張応力が作用し、板全
体が乾燥固化した後、板に歪が残る。このような
板状体を高湿雰囲気内へおくと吸湿し、その際自
重または応力が作用していると、残留歪の不釣合
いなどにより、板の変形が大きくなる。そのた
め、乾燥時に発生する残留歪を生じにくくすれば
このような欠点は消失する。多価アルコールは、
その保水性により減率乾燥時に板表面および内部
から同程度の割合で水分が失なわれるようにして
残留歪を生じさせないようにすると考えられる。
そのため、板の吸湿による変形が阻止される。 つぎに、実施例について説明する。 実施例 1 ロツクウール100部(重量基準、以下同じ)、で
んぷん8部、パラフインワツクス0.2部、アスベ
スト3部、エチレングリコール63部(得られた板
状体中にはでんぷんに対し20%(重量基準、以下
同じ)含まれることになる)に水を加えて撹拌し
濃度3.0%のスラリーをつくる。これを20メツシ
ユの金網の底をもつふるい箱で過し、さらに
0.5Kg/cm2の圧力を加えて圧搾してマツトをつく
る。このマツトには水が45%含まれている。この
マツトを150℃の熱風乾燥機中で乾燥すると、比
重0.40、厚さ12mmの繊維質板が得られた。 比較例 エチレングリコールを添加しない外は実施例1
と同様にして繊維質板を得た。 実施例1および比較例で得た繊維質板からそれ
ぞれ吸湿変形試験用試料(幅100mm、長さ700mm、
厚さ10mm)および吸湿後の弾性率測定用試料(幅
30mm、長さ100mm、厚さ10mm)を切り取り吸湿変
形試験および吸湿後の弾性率測定に供した。吸湿
変形試験は、支点間距離600mmの支点に試料をわ
たしておき、吸湿によつて自重で変形した後
(24h)、中央部分の低下距離を測つた。このとき
の雰囲気は、温度30℃、相対湿度90%に設定し
た。弾性率の測定は、この条件下で24時間放置
後、曲げ弾性率を求めた。測定結果は、吸湿変形
量が、実施例1で1.5mm、比較例で16mmであり、
曲げ弾性率が実施例1で300Kg/cm2、比較例で340
Kg/cm2であつた。すなわち、曲げ弾性率は両者と
も差がないが、吸湿変形量は実施例1が著しく小
さい。 実施例 2〜8 多価アルコールの種類および添加量を次表のよ
うに変えた外は実施例1と同様にして繊維質板を
つくり、それらの吸湿変形試験の結果を同表に示
した。
The present invention relates to a method for manufacturing a fibrous plate-like body. Conventionally, fibrous plates have been manufactured by bonding fibrous materials such as rock wool and glass wool with a starch binder. However, starch has high hygroscopicity, and the elastic modulus of starch in a hygroscopic state decreases, so that the fibrous plate-like material that has absorbed moisture is easily deformed. In order to solve this problem, the first method proposed is to use other binders instead of starch binders, or to use starch and other binders together. In this case, other binders include emulsions such as acrylic resins and vinyl acetate resins, melamine resins, epoxy resins, urea resins, and phenol resins. As a second method, a method has been proposed in which the other binder mentioned above is coated on the surface of a plate-shaped body using starch as a binder to prevent deformation due to moisture absorption. However, these methods have the following drawbacks. That is, (1) the moisture absorption deformation prevention effect may be small.
(2) Increasing the effect of preventing moisture absorption and deformation increases the cost. (3) The second method complicates the manufacturing process. Therefore, an object of the present invention is to provide a method for producing a fibrous plate-like body free of such drawbacks. The characteristics of this invention include a polyhydric alcohol with a molecular weight of 1000 or less selected from the group consisting of ethylene glycol, propylene glycol, butanediol, pentanediol, glycerin, pentaerythritol, polyethylene glycol, and polypropylene glycol, starch, and a fibrous material. and,
The present invention provides a method for producing a fibrous plate-like material, which comprises making a wet mat from a mixture with water and drying the wet mat. Next, this invention will be explained in detail. Examples of the fibrous material used in this invention include rock wool, glass wool, asbestos, and pulp. As the low molecular weight polyhydric alcohol, ethylene glycol, propylene glycol, butanediol, pentanediol, glycerin, pentaerythritol, polyethylene glycol, polypropylene glycol, etc. are used. Their molecular weight is preferably 1000 or less. Such things are
It is soluble in water, compatible with starch, and relatively inexpensive. During the production of fibrous plate-like bodies, it does not react with starch or fibrous materials, does not change its quality, and has the property of not easily volatilizing during production. The mixing amount of such polyhydric alcohol is suitably 3 to 60%, preferably 5 to 30%, based on the weight of starch. If it is less than 3%, the effect will be small, and if it is more than 60%, the properties as a binder under normal conditions, such as strength, will deteriorate, which is not desirable. The reason why the moisture resistance of the fibrous plates is improved by adding such a polyhydric alcohol to the starch binder is considered to be as follows. That is, fibrous plates are usually manufactured by making wet plates with a thickness of 5 to 20 mm from a mixture of the compound and water and drying them. During this time, it gelatinizes, dries, and solidifies. In the drying process, at the beginning, moisture is uniformly reduced from the entire board during constant rate drying, but when the process moves to lapse rate drying, the areas near the surface of the board lose moisture faster than the central area. As a result, the plate surface tends to contract and is subjected to tensile stress. As the drying progresses further, tensile stress acts inside the board, and after the entire board is dried and solidified, distortion remains in the board. When such a plate-shaped body is placed in a high-humidity atmosphere, it absorbs moisture, and if its own weight or stress is applied at that time, the plate deforms greatly due to unbalance of residual strain. Therefore, if the residual strain that occurs during drying is made less likely to occur, these defects will disappear. Polyhydric alcohol is
It is thought that due to its water-retaining properties, water is lost at the same rate from the board surface and inside during lapse rate drying, thereby preventing residual strain from occurring.
Therefore, deformation of the plate due to moisture absorption is prevented. Next, examples will be described. Example 1 100 parts of rock wool (based on weight, the same applies hereinafter), 8 parts of starch, 0.2 parts of paraffin wax, 3 parts of asbestos, 63 parts of ethylene glycol (20% of starch (based on weight) in the obtained plate-shaped body) , hereinafter the same)) and stir to create a slurry with a concentration of 3.0%. Pass this through a sieve box with a 20 mesh wire mesh bottom, and then
Matsuto is made by squeezing with a pressure of 0.5Kg/ cm2 . This pine tree contains 45% water. When this mat was dried in a hot air dryer at 150°C, a fibrous board with a specific gravity of 0.40 and a thickness of 12 mm was obtained. Comparative example Example 1 except that ethylene glycol was not added
A fibrous board was obtained in the same manner as above. Samples for moisture absorption deformation test (width 100 mm, length 700 mm,
(thickness: 10 mm) and sample for elastic modulus measurement after moisture absorption (width:
A piece (30 mm long, 100 mm long, 10 mm thick) was cut out and subjected to moisture absorption deformation tests and elastic modulus measurements after moisture absorption. In the moisture absorption deformation test, a sample was placed on a fulcrum with a distance of 600 mm between the fulcrums, and after deforming under its own weight due to moisture absorption (24 hours), the distance of decline in the center portion was measured. The atmosphere at this time was set at a temperature of 30°C and a relative humidity of 90%. The elastic modulus was measured by leaving the sample under these conditions for 24 hours, and then determining the bending elastic modulus. The measurement results showed that the amount of deformation due to moisture absorption was 1.5 mm in Example 1 and 16 mm in Comparative Example.
Flexural modulus is 300Kg/cm 2 in Example 1 and 340 in Comparative Example
It was Kg/ cm2 . That is, although there is no difference in the bending elastic modulus between the two, the amount of deformation due to moisture absorption is significantly smaller in Example 1. Examples 2 to 8 Fibrous boards were prepared in the same manner as in Example 1, except that the type and amount of polyhydric alcohol added were changed as shown in the following table, and the results of the moisture absorption deformation test are shown in the same table.

【表】【table】

【表】 以上のように、この発明の製造方法によれば、
コストを高めることなく、吸湿による変形の小さ
い繊維質板状体を容易に製造することができる。
[Table] As described above, according to the manufacturing method of the present invention,
A fibrous plate-like body that is less deformed due to moisture absorption can be easily manufactured without increasing costs.

Claims (1)

【特許請求の範囲】 1 エチレングリコール、プロピレングリコー
ル、ブタンジオール、ペンタンジオール、グリセ
リン、ペンタエリスリトール、ポリエチレングリ
コールおよびポリプロピレングリコールよりなる
群から選ばれた分子量1000以下の多価アルコール
と、でんぷんと、繊維質材料と、水との混合物か
らウエツトマツトをつくり、このウエツトマツト
を乾燥させることを特徴とする繊維質板状体の製
造方法。 2 前記多価アルコールが前記でんぷんに対して
3〜60重量%混合されている特許請求の範囲第1
項記載の繊維質板状体の製造方法。
[Scope of Claims] 1. A polyhydric alcohol with a molecular weight of 1000 or less selected from the group consisting of ethylene glycol, propylene glycol, butanediol, pentanediol, glycerin, pentaerythritol, polyethylene glycol, and polypropylene glycol, starch, and fibrous material. 1. A method for producing a fibrous plate-like material, which comprises making a wet mat from a mixture of a material and water, and drying the wet mat. 2. Claim 1, wherein the polyhydric alcohol is mixed in an amount of 3 to 60% by weight with respect to the starch.
A method for producing a fibrous plate-like body as described in .
JP8550777A 1977-07-15 1977-07-15 Manufacture of fibreboards Granted JPS5420068A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8550777A JPS5420068A (en) 1977-07-15 1977-07-15 Manufacture of fibreboards

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8550777A JPS5420068A (en) 1977-07-15 1977-07-15 Manufacture of fibreboards

Publications (2)

Publication Number Publication Date
JPS5420068A JPS5420068A (en) 1979-02-15
JPS6149438B2 true JPS6149438B2 (en) 1986-10-29

Family

ID=13860836

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8550777A Granted JPS5420068A (en) 1977-07-15 1977-07-15 Manufacture of fibreboards

Country Status (1)

Country Link
JP (1) JPS5420068A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2709485B1 (en) * 1993-08-30 1995-11-17 Arjo Wiggins Sa Mineral veil.

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE788686A (en) * 1971-09-15 1973-03-12 Agfa Gevaert Nv ISCHE MATERIALEN VERPAKKINGSPAPIER VOOR STRALINGSGEVOELIGE FOTOGRAF
JPS5281388A (en) * 1975-12-29 1977-07-07 Okura Industrial Co Ltd Process for manufacturing fiberboard

Also Published As

Publication number Publication date
JPS5420068A (en) 1979-02-15

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