JPH11269449A - Binder composition for glass wool or rock wool heat insulation material - Google Patents

Binder composition for glass wool or rock wool heat insulation material

Info

Publication number
JPH11269449A
JPH11269449A JP9086098A JP9086098A JPH11269449A JP H11269449 A JPH11269449 A JP H11269449A JP 9086098 A JP9086098 A JP 9086098A JP 9086098 A JP9086098 A JP 9086098A JP H11269449 A JPH11269449 A JP H11269449A
Authority
JP
Japan
Prior art keywords
water
urea
phenolic resin
glass wool
binder composition
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.)
Pending
Application number
JP9086098A
Other languages
Japanese (ja)
Inventor
Yoshiaki Kurimoto
好章 栗本
Kanji Osakabe
勘二 長壁
Hideki Watanabe
英樹 渡辺
Tomoaki Butani
友章 部谷
Tetsuya Horiguchi
哲也 堀口
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.)
Gun Ei Chemical Industry Co Ltd
Original Assignee
Gun Ei Chemical Industry Co 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 Gun Ei Chemical Industry Co Ltd filed Critical Gun Ei Chemical Industry Co Ltd
Priority to JP9086098A priority Critical patent/JPH11269449A/en
Publication of JPH11269449A publication Critical patent/JPH11269449A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a binder which can perfectly cure in a low-temperature region and requires a small quantity of heat when it is cured by incorporating a cure accelerator being sodium carbonate in a water-soluble phenolic resin containing and urea. SOLUTION: There is provided a binder composition prepared by adding 0.5-5 pts.wt. sodium carbonate as a cure accelerator to 100 pts.wt. solid matter of a urea-modified phenolic resin premix solution prepared by mixing a water-soluble phenolic resin with urea in a solid matter ratio of 50/50 to 100/1, and subjecting the mixture to a premix reaction at 25-40 deg.C for a specified time. A specified amount of this composition is sprayed onto a glass wool or rock wool heat insulation material, and the assemblage is cured by heating at 200-220 deg.C with e.g. hot press. The water-soluble phenolic resin is produced by mixing 1 mol of phenol with 1-5 mol of formaldehyde, adjusting the reaction system to a pH of 7.5-12.0 by the addition of a basic catalyst, and reacting the reaction system at 50-100 deg.C for a specified time.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は断熱材用バインダーに関
し、更に詳しくは作業性に優れ、高強度を与えるグラス
ウール又はロックウール断熱材用バインダー組成物に関
するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a binder for a heat insulating material, and more particularly to a binder composition for a glass wool or a rock wool heat insulating material which is excellent in workability and gives high strength.

【0002】[0002]

【従来の技術】グラスウール又はロックウールよりなる
断熱材、吸音材等はその優れた特性により住宅、設備等
に幅広く用いられている。それらの機械的強度を向上さ
せるため、又その形状を保持させるためバインダーとし
て主に水溶性フェノール樹脂が使用されている。
2. Description of the Related Art Heat insulating materials and sound absorbing materials made of glass wool or rock wool are widely used in houses, facilities and the like due to their excellent characteristics. Water-soluble phenolic resins are mainly used as binders to improve their mechanical strength and to maintain their shapes.

【0003】数年来、バインダー費用を低減させるた
め、水溶性フェノール樹脂を尿素で変性することが常用
されている。さらに尿素は、アンモニアのように遊離ホ
ルムアルデヒドと結合する特性を有する。水溶性フェノ
ール樹脂の尿素による変性は、すでにこの分野ではフェ
ノール樹脂の製造時に、又は断熱材の加工直前に実施さ
れている。
For several years, it has been customary to modify water-soluble phenolic resins with urea in order to reduce binder costs. In addition, urea has the property of binding free formaldehyde like ammonia. The modification of water-soluble phenolic resins with urea has already been carried out in the field during the production of phenolic resins or shortly before the processing of insulation.

【0004】グラスウール又はロックウールの原料とし
て適当なのが、ガラス、玄武岩、及び種々のクリンカ材
料などである。これら原料が溶融されかつ繊維に加工さ
れ、これにその加工された場所でフェノール樹脂水溶液
が噴霧され、かつ引き続き集綿室の底部でコンベアベル
トに吸引される。得られたフェルトが圧縮されかつコン
ベアベルトとともに硬化室を経て搬送される。そこでフ
ェノール樹脂が、下方からマットを経て流動する熱風に
より硬化される。
Suitable raw materials for glass or rock wool include glass, basalt, and various clinker materials. These raw materials are melted and processed into fibers, where the aqueous phenolic resin solution is sprayed and subsequently sucked on the conveyor belt at the bottom of the cotton collecting chamber. The resulting felt is compressed and conveyed with a conveyor belt through a curing chamber. There, the phenolic resin is cured by hot air flowing from below through the mat.

【0005】さらに、高縮合反応を促進させるため硫酸
アンモニウム等のアンモニウム塩が硬化促進剤として用
いられている。この硬化促進剤は水溶性フェノール樹脂
と尿素との合計固形分100部に対して1〜5部フェノ
ール樹脂の製造時に、又は断熱材の加工直前に添加され
ている。
Further, an ammonium salt such as ammonium sulfate is used as a curing accelerator to promote a high condensation reaction. The curing accelerator is added in an amount of 1 to 5 parts based on 100 parts of the total solid content of the water-soluble phenol resin and urea at the time of producing the phenol resin or immediately before processing the heat insulating material.

【0006】しかし、硬化促進剤を添加し硬化反応を促
進させているが、硬化に必要な熱量は高く、200〜2
80℃程度の熱風を用いている。また、200℃程度の
低温域で製造されているグラスウール又はロックウール
断熱材の強度は280℃程度の高温域で硬化したものに
比べ低くなっている。
However, although a curing accelerator is added to accelerate the curing reaction, the amount of heat required for curing is high,
Hot air of about 80 ° C. is used. Further, the strength of the glass wool or rock wool heat insulating material manufactured in a low temperature range of about 200 ° C. is lower than that of a material cured in a high temperature range of about 280 ° C.

【0007】[0007]

【本発明が解決しようとする課題】硬化促進剤として従
来用いられていた硫酸アンモニウム等のアンモニウム塩
を炭酸ナトリウムに替えることによって、200〜22
0℃の低温域での完全な硬化を可能にし、その結果硬化
に必要な熱量は低く抑えることができ、低コストのグラ
スウール又はロックウール断熱材用バインダーを得るこ
とを可能にしたものである。
By replacing an ammonium salt such as ammonium sulfate, which has been conventionally used as a curing accelerator, with sodium carbonate, it is possible to obtain a curing agent having a viscosity of 200 to 22%.
The present invention enables complete curing in a low temperature range of 0 ° C., and as a result, the amount of heat required for curing can be kept low, thereby making it possible to obtain a low-cost binder for glass wool or rock wool insulation.

【0008】[0008]

【課題を解決するための手段】本発明はフェノール樹脂
水溶液に硬化促進剤として炭酸ナトリウムを添加した樹
脂よりなるグラスウール又はロックウール断熱材用バイ
ンダー組成物である。
SUMMARY OF THE INVENTION The present invention is a binder composition for a glass wool or rock wool heat insulating material comprising a resin obtained by adding sodium carbonate as a curing accelerator to an aqueous phenol resin solution.

【0009】本発明に用いられる水溶性フェノール樹脂
は一般的にグラスウールやロックウール断熱材のバイン
ダーとして用いられる水溶性フェノール樹脂が使用可能
である。
As the water-soluble phenol resin used in the present invention, a water-soluble phenol resin generally used as a binder for a glass wool or a rock wool heat insulating material can be used.

【0010】即ち、フェノール1モルに対してホルムア
ルデヒドを1〜5モル加え、塩基性触媒を加えpH7.
5〜12.0に反応系を調整し、50〜100℃で所定
時間反応して得られるものである。これらは必要に応
じ、中和、濃縮、希釈、及び濾過等の工程が加えられ製
造されるものである。
That is, 1 to 5 moles of formaldehyde are added to 1 mole of phenol, and a basic catalyst is added to adjust the pH to 7.
It is obtained by adjusting the reaction system to 5 to 12.0 and reacting at 50 to 100 ° C. for a predetermined time. These are manufactured by adding processes such as neutralization, concentration, dilution, and filtration as needed.

【0011】この水溶性フェノール樹脂と尿素との固形
分比が50:50〜100:0までの範囲になるように
尿素を加え、25〜40℃で所定時間プレミックス反応
を行い、尿素による変性を行っている。
Urea is added so that the solid content ratio of the water-soluble phenolic resin and urea is in the range of 50:50 to 100: 0, and a premix reaction is performed at 25 to 40 ° C. for a predetermined time, and denaturation with urea is performed. It is carried out.

【0012】解決策となる硬化促進剤は水溶性フェノー
ル樹脂製造直後、又は断熱材加工直前に添加されてい
る。硬化促進剤の添加量は水溶性フェノール樹脂と尿素
とのプレミックス液の合計固形分100部に対して5部
を越える場合は硬化促進作用は飽和状態になり、逆に添
加量が0.5部未満の場合は硬化促進作用は現れない。
よって硬化促進剤の炭酸ナトリウムは水溶性フェノール
樹脂と尿素とのプレミックス液の合計固形分100部に
対して0.5〜5部の添加量が望ましい。
The curing accelerator which is a solution is added immediately after the production of the water-soluble phenol resin or immediately before processing the heat insulating material. When the addition amount of the curing accelerator exceeds 5 parts with respect to the total solid content of 100 parts of the premix liquid of the water-soluble phenol resin and urea, the curing acceleration effect becomes saturated, and conversely, the addition amount is 0.5%. If the amount is less than 10 parts, no hardening promoting effect appears.
Therefore, the addition amount of sodium carbonate as a curing accelerator is preferably 0.5 to 5 parts with respect to 100 parts of the total solid content of the premix liquid of the water-soluble phenol resin and urea.

【0013】[0013]

【実施例】以下に実施例を挙げて本発明を具体的に説明
するが、本発明はこれらに限定されるものではない。な
お、実施例中の部および%は特に断りのない限り重量基
準である。
EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to these examples. The parts and percentages in the examples are on a weight basis unless otherwise specified.

【0014】[合成例1]温度計、コンデンサー付きの
三口フラスコにフェノール100g、50%ホルムアル
デヒド水溶液191.3g、水酸化バリウム10gを仕
込み、攪拌しながら60℃まで加熱し、その後60℃で
3時間反応を行った。次いで30%硫酸水溶液19gを
加え反応系を中和し、反応を終了させ冷却し水溶性フェ
ノール樹脂を得た。
Synthesis Example 1 A three-necked flask equipped with a thermometer and a condenser was charged with 100 g of phenol, 191.3 g of a 50% aqueous formaldehyde solution, and 10 g of barium hydroxide, and heated to 60 ° C. with stirring, and then at 60 ° C. for 3 hours. The reaction was performed. Next, 19 g of a 30% sulfuric acid aqueous solution was added to neutralize the reaction system, the reaction was terminated, and the mixture was cooled to obtain a water-soluble phenol resin.

【0015】得られた樹脂の特性は、不揮発分45%、
水希釈率20倍以上、pH7.3、遊離ホルムアルデヒ
ド10%であった。
The characteristics of the obtained resin are as follows:
Water dilution ratio was 20 times or more, pH was 7.3, and free formaldehyde was 10%.

【0014】[合成例2]合成例1で得られた水溶性フ
ェノール樹脂100gに40%尿素水溶液75gを混合
し、攪拌しながら30℃まで加熱し、その後30℃で2
時間プレミックス反応を行った。反応後25%アンモニ
ア水を加え、pH9.0に調整した。
[Synthesis Example 2] 100 g of the water-soluble phenol resin obtained in Synthesis Example 1 was mixed with 75 g of a 40% aqueous urea solution, heated to 30 ° C. with stirring, and then heated at 30 ° C.
A time premix reaction was performed. After the reaction, 25% aqueous ammonia was added to adjust the pH to 9.0.

【0017】さらに硬化促進剤として25%硫酸アンモ
ニウム水溶液を9.0g加え、調合液を得た。
Further, 9.0 g of a 25% aqueous solution of ammonium sulfate was added as a curing accelerator to obtain a preparation.

【0018】[合成例3]合成例2と同様にプレミック
ス反応を行い、反応後25%アンモニア水を加え、pH
9.0に調整した。さらに硬化促進剤として25%炭酸
ナトリウム水溶液を9.0g加え、調合液を得た。
[Synthesis Example 3] A premix reaction was performed in the same manner as in Synthesis Example 2. After the reaction, 25% aqueous ammonia was added,
It was adjusted to 9.0. Further, 9.0 g of a 25% aqueous sodium carbonate solution was added as a curing accelerator to obtain a preparation.

【0019】[実施例1]合成例3で得られた調合液の
水溶性フェノール樹脂と尿素との合計固形分が10%に
なるように水で希釈し、溶融紡糸したグラスウールに吹
き付け、ホットプレスを用いて200〜220℃で各1
0〜40分間硬化させ密度32kg/m3のグラスウー
ル断熱材を得た。
[Example 1] The mixture prepared in Synthesis Example 3 was diluted with water so that the total solid content of the water-soluble phenolic resin and urea was 10%, sprayed onto melt-spun glass wool, and hot-pressed. Each at 200-220 ° C using
The mixture was cured for 0 to 40 minutes to obtain a glass wool heat insulating material having a density of 32 kg / m 3 .

【0020】[比較例1]合成例2で得られた調合液の
水溶性フェノール樹脂と尿素との合計固形分が10%に
なるように水で希釈し、溶融紡糸したグラスウールに吹
き付け、ホットプレスを用いて200〜220℃で各1
0〜40分間硬化させ密度32kg/m3のグラスウー
ル断熱材を得た。
[Comparative Example 1] The solution prepared in Synthesis Example 2 was diluted with water so that the total solid content of the water-soluble phenolic resin and urea was 10%, sprayed on melt-spun glass wool, and hot-pressed. Each at 200-220 ° C using
The mixture was cured for 0 to 40 minutes to obtain a glass wool heat insulating material having a density of 32 kg / m 3 .

【0021】実施例1および比較例1で得られたグラス
ウール断熱材の高さの20%圧縮したときにかかる負荷
を求め、圧縮強度を算出した。
The load applied when the glass wool heat insulating material obtained in Example 1 and Comparative Example 1 was compressed by 20% of the height was determined, and the compressive strength was calculated.

【0022】硬化温度の違いによるグラスウール断熱材
の圧縮強度を表1〜3に記した。
Tables 1 to 3 show the compressive strengths of the glass wool insulating materials depending on the curing temperature.

【0023】[0023]

【表1】200℃硬化による圧縮強度(kgf/m2 [Table 1] Compressive strength by curing at 200 ° C (kgf / m 2 )

【0024】[0024]

【表2】210℃硬化による圧縮強度(kgf/m2 Table 2 Compressive strength by curing at 210 ° C (kgf / m 2 )

【0025】[0025]

【表3】220℃硬化による圧縮強度(kgf/m2 Table 3 Compressive strength by curing at 220 ° C (kgf / m 2 )

【0026】[0026]

【発明の効果】炭酸ナトリウムをグラスウール又はロッ
クウール断熱材用バインダーの硬化促進剤として用いる
ことによって、200〜220℃の低温域で完全な樹脂
の硬化を可能にし、結果として機械的強度に優れた低コ
ストのグラスウール又はロックウール断熱材用バインダ
ーを得ることが出来る。
By using sodium carbonate as a curing accelerator for a binder for glass wool or rock wool insulation, it is possible to completely cure the resin in a low temperature range of 200 to 220 ° C., resulting in excellent mechanical strength. A low cost binder for glass wool or rock wool insulation can be obtained.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 部谷 友章 群馬県高崎市宿大類町700番地 群栄化学 工業株式会社内 (72)発明者 堀口 哲也 群馬県高崎市宿大類町700番地 群栄化学 工業株式会社内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Tomoaki Motoya 700 Sukuodaizaimachi, Takasaki City, Gunma Prefecture Inside Gunei Chemical Industry Co., Ltd. Inside the corporation

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】バインダーの硬化促進剤として炭酸ナトリ
ウムを用いる水溶性フェノール樹脂及び尿素からなるグ
ラスウール又はロックウール断熱材用バインダー組成
物。
1. A binder composition for heat insulating glass wool or rock wool, comprising a water-soluble phenol resin using sodium carbonate as a curing accelerator for the binder and urea.
【請求項2】水溶性フェノール樹脂と尿素との混合割合
が固形分比で50:50〜100:0までの範囲からな
る請求項1記載のグラスウール又はロックウール断熱材
用バインダー組成物。
2. The glass wool or rock wool heat insulating binder composition according to claim 1, wherein the mixing ratio of the water-soluble phenol resin and urea is in the range of 50:50 to 100: 0 in terms of solid content ratio.
【請求項3】炭酸ナトリウムが水溶性フェノール樹脂と
尿素との合計固形分100部に対して0.5〜5部添加
してなる請求項2記載のグラスウール又はロックウール
断熱材用バインダー組成物。
3. The binder composition for glass wool or rock wool insulation according to claim 2, wherein sodium carbonate is added in an amount of 0.5 to 5 parts based on 100 parts of the total solid content of the water-soluble phenol resin and urea.
JP9086098A 1998-03-19 1998-03-19 Binder composition for glass wool or rock wool heat insulation material Pending JPH11269449A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9086098A JPH11269449A (en) 1998-03-19 1998-03-19 Binder composition for glass wool or rock wool heat insulation material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9086098A JPH11269449A (en) 1998-03-19 1998-03-19 Binder composition for glass wool or rock wool heat insulation material

Publications (1)

Publication Number Publication Date
JPH11269449A true JPH11269449A (en) 1999-10-05

Family

ID=14010322

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9086098A Pending JPH11269449A (en) 1998-03-19 1998-03-19 Binder composition for glass wool or rock wool heat insulation material

Country Status (1)

Country Link
JP (1) JPH11269449A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008145068A (en) * 2006-12-12 2008-06-26 Daikin Ind Ltd Refrigerant piping for heat exchanger
JP2008151422A (en) * 2006-12-18 2008-07-03 Daikin Ind Ltd Heat exchanger
KR101100733B1 (en) * 2011-03-22 2012-01-05 (주)모린스코퍼레이션 Manufacturing method of fireproof binder for e-glass fiber heat insulating materials forming

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008145068A (en) * 2006-12-12 2008-06-26 Daikin Ind Ltd Refrigerant piping for heat exchanger
JP2008151422A (en) * 2006-12-18 2008-07-03 Daikin Ind Ltd Heat exchanger
KR101100733B1 (en) * 2011-03-22 2012-01-05 (주)모린스코퍼레이션 Manufacturing method of fireproof binder for e-glass fiber heat insulating materials forming

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