JPH08253613A - Synthetic resin foam - Google Patents
Synthetic resin foamInfo
- Publication number
- JPH08253613A JPH08253613A JP5758595A JP5758595A JPH08253613A JP H08253613 A JPH08253613 A JP H08253613A JP 5758595 A JP5758595 A JP 5758595A JP 5758595 A JP5758595 A JP 5758595A JP H08253613 A JPH08253613 A JP H08253613A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- foam
- product
- synthetic resin
- cured product
- 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
Links
- 239000006260 foam Substances 0.000 title claims abstract description 43
- 229920003002 synthetic resin Polymers 0.000 title claims abstract description 14
- 239000000057 synthetic resin Substances 0.000 title claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 28
- 239000011347 resin Substances 0.000 claims abstract description 28
- 239000005011 phenolic resin Substances 0.000 claims abstract description 23
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 15
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 238000005187 foaming Methods 0.000 claims abstract description 10
- 239000003822 epoxy resin Substances 0.000 claims abstract description 9
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims abstract description 8
- 230000002950 deficient Effects 0.000 claims abstract description 6
- 238000000465 moulding Methods 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract 2
- 239000000843 powder Substances 0.000 claims description 16
- 239000012778 molding material Substances 0.000 claims description 6
- 239000006261 foam material Substances 0.000 claims description 5
- 239000011159 matrix material Substances 0.000 claims 2
- 238000010298 pulverizing process Methods 0.000 claims 1
- 229920001568 phenolic resin Polymers 0.000 abstract description 7
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 5
- 230000007613 environmental effect Effects 0.000 abstract description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000004064 recycling Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 8
- 230000005484 gravity Effects 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920003987 resole Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 239000008258 liquid foam Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、フェノール樹脂成形材
料硬化物等の熱硬化性樹脂硬化物の粉末を配合剤として
含有する合成樹脂発泡体に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a synthetic resin foam containing, as a compounding agent, a powder of a thermosetting resin cured product such as a cured product of a phenol resin molding material.
【0002】[0002]
【従来の技術】従来、合成樹脂発泡体としてはポリスチ
レンフォーム、ポリエチレンフォーム、ポリプロピレン
フォーム、塩化ビニルフォーム等の熱可塑性樹脂発泡体
やポリウレタンフォーム、フェノール樹脂フォーム、エ
ポキシ樹脂フォーム、ユリア樹脂フォーム等の熱硬化性
樹脂発泡体等があり、断熱性、緩衝性、クッション性、
音響特性(吸音性、遮音性)、浮揚性等に優れているた
め、建築、車両、船舶用断熱材、包装材料、マットレ
ス、自動車用シート、椅子などのクッション材、船舶用
の救命器具や浮子、建築の吸音用壁や遮音パネル等、目
的・用途に応じて広い分野で使用されている。2. Description of the Related Art Conventionally, as synthetic resin foams, thermoplastic foams such as polystyrene foam, polyethylene foam, polypropylene foam and vinyl chloride foam and polyurethane foam, phenol resin foam, epoxy resin foam, urea resin foam and the like have been used. There are curable resin foams, etc., which have heat insulation, cushioning, cushioning,
Due to its excellent acoustic properties (sound absorption, sound insulation), buoyancy, etc., it is used for building, vehicles, heat insulation materials for ships, packaging materials, mattresses, car seats, cushioning materials for chairs, lifesaving devices for ships and floats. It is used in a wide range of fields, such as sound absorbing walls and sound insulation panels for construction, depending on the purpose and application.
【0003】これらの発泡体は樹脂のみで発泡体を形成
する場合もあり、また充填剤を含有する場合もある。充
填剤を配合する場合、通常充填剤は樹脂単独の場合の発
泡体の欠点を改良するために加えられる。発泡体に配合
される充填剤は目的により種々のものがあるが、耐熱性
を向上する目的に対しては従来無機質のものが多く使用
されてきた。しかし、液状の発泡材組成物を使用する場
合、無機質充填剤は発泡体に使用される樹脂に比べ比重
が大であり、発泡作業時にその比重差により沈降して底
部にたまりやすいため均質な組成の発泡体が得られにく
いという問題があった。These foams sometimes form a foam only with a resin, and may contain a filler. When a filler is included, it is usually added to improve the drawbacks of the foam when the resin alone is used. There are various fillers to be blended in the foam, depending on the purpose. For the purpose of improving heat resistance, inorganic fillers have been used in many cases. However, when a liquid foam material composition is used, the inorganic filler has a larger specific gravity than the resin used for the foam, and during the foaming operation, it tends to settle at the bottom due to the difference in the specific gravity, resulting in a homogeneous composition. There was a problem that it was difficult to obtain the foam.
【0004】[0004]
【発明が解決しようとする課題】本発明者は、熱硬化性
樹脂硬化物の粉末を合成樹脂発泡材組成物に配合するこ
とにより発泡組織の均質化をはかることができることを
見出し、本発明を完成したものである。DISCLOSURE OF THE INVENTION The present inventor has found that the foamed structure can be homogenized by adding a powder of a thermosetting resin cured product to a synthetic resin foam material composition, and the present invention has been made. It has been completed.
【0005】[0005]
【課題を解決するための手段】本発明は、合成樹脂発泡
材組成物中に熱硬化性樹脂硬化物粉末を配合し発泡させ
てなる発泡体に関するものである。SUMMARY OF THE INVENTION The present invention relates to a foam obtained by blending a thermosetting resin cured product powder in a synthetic resin foam material composition and expanding the composition.
【0006】熱硬化性樹脂硬化物としてはフェノール樹
脂、エポキシ樹脂、ポリウレタン樹脂等の熱硬化性樹脂
成形材料で成形品を成形する際に生じるスプルー・ラン
ナー又は成形不良品、あるいは使用済品、又はフェノー
ル樹脂、エポキシ樹脂等の熱硬化性樹脂積層板の端材又
は不良品、あるいは使用済品等を使用すれば、これまで
廃棄されていた資源の有効利用ともなり好ましい。発泡
体は各種用途に使用されているが、最近特に建築物、車
両、自動車等の防音、断熱のために使用される発泡体に
ついて火災に対する安全性を向上するため耐熱性、耐燃
性、耐煙性に対する要求が強くなってきた。この要求に
対しては発泡体の中でもフェノール樹脂は上記のいずれ
の特性も特に良好であり注目されている。As the thermosetting resin cured product, a sprue runner or a defective product produced when molding a molded product with a thermosetting resin molding material such as phenol resin, epoxy resin, polyurethane resin, or a used product, or It is preferable to use a scrap material or a defective product of a thermosetting resin laminated plate such as a phenol resin or an epoxy resin, or a used product because it effectively utilizes the resources that have been discarded until now. Foams are used for various purposes, but heat resistance, flame resistance, and smoke resistance for foams used recently for soundproofing and heat insulation of buildings, vehicles, automobiles, etc. in order to improve safety against fire. The demand for sex has become stronger. In response to this requirement, among the foamed products, phenolic resins have attracted attention because they are particularly good in all of the above properties.
【0007】フェノール樹脂発泡体は合成樹脂発泡体の
中では最高の耐熱性を示すものであるが、さらに耐熱性
を向上するために種々検討が行われている。フェノール
樹脂発泡体を製造する方法としては、液状レゾール樹脂
を使用し、これに酸性硬化剤、整泡剤、揮発性溶剤を加
えて発泡する方法と、固形ノボラック樹脂に硬化剤であ
るヘキサメチレンテトラミン及び加熱時にガスを発生す
る固形発泡剤を加えて微粉末化し、これを加熱発泡する
方法とがある。The phenolic resin foam has the highest heat resistance among synthetic resin foams, but various studies have been conducted to further improve the heat resistance. As a method for producing a phenolic resin foam, a liquid resol resin is used, and an acidic curing agent, a foam stabilizer, and a volatile solvent are added thereto to foam, and hexamethylenetetramine, which is a curing agent for a solid novolac resin, is used. Also, there is a method in which a solid foaming agent that generates gas at the time of heating is added to make a fine powder, and this is heated and foamed.
【0008】上記のフェノール樹脂発泡体の耐熱性を高
めるためにはクレー、タルク、炭酸カルシウム、シリ
カ、アルミナ等の無機質の充填剤を加える方法も考えら
れるが、これらの無機物質はフェノール樹脂に比べて比
重が高く、樹脂の発泡時に分離し、特に液状レゾール樹
脂の場合沈降して底部にたまり、均一な組成物を作りに
くく、良好な発泡体を得ることが困難であった。In order to improve the heat resistance of the above-mentioned phenol resin foam, a method of adding an inorganic filler such as clay, talc, calcium carbonate, silica, alumina, etc. can be considered, but these inorganic substances are more preferable than phenol resin. It has a high specific gravity and separates at the time of foaming of the resin, and particularly in the case of a liquid resol resin, it settles and accumulates at the bottom, making it difficult to form a uniform composition, and it is difficult to obtain a good foam.
【0009】本発明において、配合剤として使用する熱
硬化性樹脂硬化物粉末の中で、特にフェノール樹脂成形
材料の成形時に得られる硬化物及び積層板から得られる
硬化物は加圧された緻密構造であることから特に耐熱性
が高く、これをフェノール樹脂発泡体に配合することに
より耐熱性の良好な発泡体を得ることができる。樹脂硬
化物粉末は発泡体用樹脂に近い比重をもつことから発泡
時の偏在も殆どなく、母体である合成樹脂と均一に分散
することから組成上も特性上もにバラツキの少ない良好
な発泡体となる。In the present invention, among the thermosetting resin cured product powders used as the compounding agent, the cured product obtained at the time of molding the phenol resin molding material and the cured product obtained from the laminated plate are the dense structure having a pressure. Therefore, the heat resistance is particularly high, and by adding this to the phenol resin foam, a foam having good heat resistance can be obtained. Since the cured resin powder has a specific gravity close to that of the foam resin, there is almost no uneven distribution at the time of foaming, and because it is evenly dispersed with the synthetic resin that is the base material, there is little variation in composition and characteristics. Becomes
【0010】[0010]
〔実施例〕ノボラック型フェノール樹脂100重量部、
ヘキサメチレンテトラミン15重量部、セルマルクA
(三協化成株式会社製、成分:DPT)5重量部を加熱
ニーダーで混合後粉砕し100メッシュ以下の発泡用樹
脂粉末Aを得た。フェノール樹脂成形材料(フェノール
樹脂:粘土鉱物質フィラー=60:40重量部)の成形
時に発生するスプルー・ランナーを粉砕し100メッシ
ュ以下のフェノール樹脂硬化物粉末Pを得た。 (配 合) 発泡用樹脂粉末A:100重量部 硬化物粉末P : 20重量部 上記配合物を充分混合して型に入れ180℃にて10分
加熱し、比重 0.2の発泡体を得た。[Example] 100 parts by weight of novolac type phenol resin,
Hexamethylenetetramine 15 parts by weight, Selmark A
(Sankyo Kasei Co., Ltd., component: DPT) 5 parts by weight were mixed with a heating kneader and then pulverized to obtain a resin powder A for foaming having 100 mesh or less. The sprue runner generated during the molding of the phenol resin molding material (phenol resin: clay mineral filler = 60: 40 parts by weight) was pulverized to obtain a phenol resin cured product powder P having 100 mesh or less. (Distribution) Foaming resin powder A: 100 parts by weight Cured product powder P: 20 parts by weight The above components are thoroughly mixed and put into a mold and heated at 180 ° C. for 10 minutes to obtain a foamed product having a specific gravity of 0.2. It was
【0012】〔比較例1〕発泡用樹脂粉末Aのみを型に
入れ180℃にて10分加熱し、比重 0.2の発泡体を
得た。 〔比較例2〕 (配 合) 発泡用樹脂粉末A :100重量部 シリカ粉末(100メッシュ以下): 20重量部 上記配合物を充分混合して型に入れ180℃にて10分
加熱し、比重 0.2の発泡体を得た。 〔比較例3〕市販のウレタン発泡体(比重 0.2)を用
いて比較試験を行った。Comparative Example 1 Only foaming resin powder A was placed in a mold and heated at 180 ° C. for 10 minutes to obtain a foam having a specific gravity of 0.2. [Comparative Example 2] (Combined) Foaming resin powder A: 100 parts by weight Silica powder (100 mesh or less): 20 parts by weight The above ingredients were thoroughly mixed and put into a mold and heated at 180 ° C for 10 minutes to give a specific gravity. A foam of 0.2 was obtained. [Comparative Example 3] A comparative test was carried out using a commercially available urethane foam (specific gravity: 0.2).
【0015】以上の実施例及び比較例により得られた発
泡体について以下の特性を測定した。結果を次表に示
す。 ─────────────────────────────── 実施例 比較例1 比較例2 比較例3 ─────────────────────────────── 組織の均一性 良 良 不良 良 耐燃性 良 やや良 良 不良 耐煙性 良 良 良 不良 ───────────────────────────────The following characteristics were measured for the foams obtained in the above Examples and Comparative Examples. The results are shown in the table below. ──────────────────────────────── Example Comparative Example 1 Comparative Example 2 Comparative Example 3 ──────── ─────────────────────── Organization uniformity Good Good Bad Good Flame resistance Good Fair Good Good Bad Smoke resistance Good Good Good Bad ───── ──────────────────────────
【0016】[0016]
【発明の効果】以上から明らかなように、本発明の合成
樹脂発泡体は従来のものと比較して耐燃性が良好で、組
織的にも均一で良好であった。又本発明の発泡体は本来
廃棄される熱硬化性樹脂硬化物を利用するものであり、
リサイクル製品として省資源・環境対策のために有効な
ものである。As is apparent from the above, the synthetic resin foam of the present invention has better flame resistance than the conventional one and is uniform and good in structure. Further, the foam of the present invention utilizes a thermosetting resin cured product that is originally discarded,
As a recycled product, it is effective for resource conservation and environmental measures.
Claims (5)
硬化物の粉末を配合し、発泡させてなる合成樹脂発泡
体。1. A synthetic resin foam obtained by blending a thermosetting resin cured product powder in a synthetic resin foam material composition and foaming.
脂成形材料又はエポキシ樹脂成形材料の成形時に発生す
るスプルー・ランナー、カル・ランナー又は成形不良
品、あるいは使用済品を粉砕したものである請求項1記
載の発泡体。2. The cured thermosetting resin powder is a sprue runner, cull runner or defective molding product generated during molding of a phenol resin molding material or an epoxy resin molding material, or a crushed product of a used product. Item 1. A foam according to item 1.
脂積層板又はエポキシ樹脂積層板の端材又は不良品、あ
るいは使用済品を粉砕したものである請求項1記載の発
泡体。3. The foam according to claim 1, wherein the thermosetting resin cured product powder is obtained by pulverizing a scrap material or a defective product of a phenol resin laminated plate or an epoxy resin laminated plate, or a used product.
樹脂、エポキシ樹脂、ウレタン樹脂等の熱硬化性樹脂で
ある請求項1記載の発泡体。4. The foam according to claim 1, wherein the matrix component of the foam material composition is a thermosetting resin such as phenol resin, epoxy resin or urethane resin.
脂である請求項4記載の発泡体。5. The foam according to claim 4, wherein the matrix component of the foam material composition is a phenol resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5758595A JPH08253613A (en) | 1995-03-16 | 1995-03-16 | Synthetic resin foam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5758595A JPH08253613A (en) | 1995-03-16 | 1995-03-16 | Synthetic resin foam |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH08253613A true JPH08253613A (en) | 1996-10-01 |
Family
ID=13059932
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5758595A Pending JPH08253613A (en) | 1995-03-16 | 1995-03-16 | Synthetic resin foam |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH08253613A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20040005035A (en) * | 2002-07-08 | 2004-01-16 | (주) 나노텍 | Recycling Phenol Foam Complex |
-
1995
- 1995-03-16 JP JP5758595A patent/JPH08253613A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20040005035A (en) * | 2002-07-08 | 2004-01-16 | (주) 나노텍 | Recycling Phenol Foam Complex |
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