JPH05230334A - Amino resin molding material - Google Patents
Amino resin molding materialInfo
- Publication number
- JPH05230334A JPH05230334A JP19333691A JP19333691A JPH05230334A JP H05230334 A JPH05230334 A JP H05230334A JP 19333691 A JP19333691 A JP 19333691A JP 19333691 A JP19333691 A JP 19333691A JP H05230334 A JPH05230334 A JP H05230334A
- Authority
- JP
- Japan
- Prior art keywords
- molding material
- amino resin
- resin
- parts
- resin molding
- 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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は配線器具、電気器具、厨
房器具、家庭用品、雑貨品等、特に寸法安定性、耐衝撃
性を必要とする成形品が得られるアミノ樹脂成形材料に
関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an amino resin molding material for obtaining wiring products, electric appliances, kitchen appliances, household products, miscellaneous goods, etc., particularly moldings requiring dimensional stability and impact resistance. is there.
【0002】[0002]
【従来の技術】従来、ユリア樹脂、メラミン樹脂からな
る成形品は、固く、耐汚染性が大きいので重宝されてい
るが、寸法安定性が小さいと言う問題点があった。この
為この分野ではフェノ−ル樹脂成形品が用いられている
が、明色性がないと言う問題があった。2. Description of the Related Art Conventionally, molded articles made of urea resin and melamine resin are useful because they are hard and have high stain resistance, but there is a problem in that they have low dimensional stability. For this reason, a phenol resin molded product is used in this field, but there is a problem that it has no bright color.
【0003】[0003]
【発明が解決しようとする課題】従来の技術で述べたよ
うに、アミノ樹脂成形材料では明色成形品を得ることは
出来ても、寸法安定性が小さいと言う問題点があった。
本発明は従来の技術における上述の問題点に鑑みてなさ
れたもので、その目的とするところは、寸法安定性に優
れた成形品の得られるアミノ樹脂成形材料を提供するこ
とにある。As described in the prior art, the amino resin molding material has a problem in that although it is possible to obtain a light-colored molded product, the dimensional stability is low.
The present invention has been made in view of the above problems in the prior art, and an object of the present invention is to provide an amino resin molding material from which a molded article having excellent dimensional stability can be obtained.
【0004】[0004]
【課題を解決するための手段】本発明は、アミノ樹脂溶
液にポリエチレングライコールを添加後、減圧加熱脱水
した固形アミノ樹脂を用いたことを特徴とするアミノ樹
脂成形材料のため、上記目的を達成することができたも
ので、以下本発明を詳細に説明する。Means for Solving the Problems The present invention is an amino resin molding material characterized by using a solid amino resin obtained by adding polyethylene glycol to an amino resin solution and then heating and dehydrating under reduced pressure. The present invention will be described in detail below.
【0005】本発明に用いるアミノ樹脂は、ユリア樹
脂、メラミン樹脂、グアナミン樹脂等のアミノ樹脂全般
を用いることができ、アミノ樹脂はアミノ樹脂溶液の形
態でポリエチレングライコールを添加後、減圧加熱脱水
した固形アミノ樹脂として用いるものである。ポリエチ
レングライコールの量は、アミノ樹脂100重量部(以
下単に部と記す)に対して1〜30部であることが好ま
しい。即ち1部未満では寸法安定性が向上し難く、30
部を越えると耐水性が低下する傾向にあるからである。
ポリエチレングライコールの種類は特に限定するもので
はないが、重合度4000程度のものをもちいることが
望ましい。又アミノ樹脂はエポキシ変性、フェノール変
性等の変性アミノ樹脂をも含むものである。硬化剤とし
ては無水フタル酸等を用い、樹脂100重量部(以下単
に部と記す)に対し0.01〜3部添加することが好ま
しい。離型剤としては脂肪酸、脂肪酸金属塩、ワックス
等を用い、樹脂100部に対して0.05〜5部添加す
ることが好ましい。充填剤、補強剤としてはパルプ、木
粉、ガラス繊維、炭酸カルシュム、タルク等を用いる。
更に必要に応じて着色剤が添加される。かくして上記材
料を配合、混合、混練、粉砕し、更に必要に応じて造粒
してアミノ樹脂成形材料を得るものである。該成形材料
の成形については、圧縮成形、トランスフアー成形、射
出成形等で成形するものである。As the amino resin used in the present invention, all amino resins such as urea resin, melamine resin and guanamine resin can be used. The amino resin was dehydrated by heating under reduced pressure after adding polyethylene glycol in the form of an amino resin solution. It is used as a solid amino resin. The amount of polyethylene glycol is preferably 1 to 30 parts with respect to 100 parts by weight of amino resin (hereinafter simply referred to as "part"). That is, if it is less than 1 part, it is difficult to improve the dimensional stability.
This is because the water resistance tends to decrease when the content exceeds the range.
The type of polyethylene glycol is not particularly limited, but it is desirable to use one having a degree of polymerization of about 4000. The amino resin also includes a modified amino resin such as epoxy modified or phenol modified. As a curing agent, phthalic anhydride or the like is used, and it is preferable to add 0.01 to 3 parts by weight to 100 parts by weight of the resin (hereinafter simply referred to as “part”). Fatty acids, fatty acid metal salts, waxes and the like are used as the release agent, and it is preferable to add 0.05 to 5 parts to 100 parts of the resin. As the filler and the reinforcing agent, pulp, wood powder, glass fiber, calcium carbonate, talc and the like are used.
Further, a colorant is added if necessary. Thus, the above-mentioned materials are blended, mixed, kneaded, pulverized, and further granulated as required to obtain an amino resin molding material. The molding material is molded by compression molding, transfer molding, injection molding or the like.
【0006】以下本発明を実施例に基づいて説明する。The present invention will be described below based on examples.
【0007】[0007]
【実施例1】メラミン1モルに対しホルムアルデヒド
1.6モルを加え、85℃で1時間PH9で反応させて
得たメラミン樹脂溶液100部に、ポリエチレングライ
コール(三洋化成工業株式会社製、PEG4000)2
部を添加、分散後真空度100TORRで減圧加熱脱水
して固形変性メラミン樹脂を得た。次に該固形変性メラ
ミン樹脂70部、パルプ30部、無水フタール酸0.3
部、ステアリン酸亜鉛0.8部、ステアリン酸アマイド
0.2部を配合、混合、混練、粉砕して変性メラミン樹
脂成形材料を得た。次に該成形材料をトランスファー成
形機を用いて、金型温度145℃、成形圧力100Kg
/cm2 硬化時間3分間で成形し成形品を得た。Example 1 1.6 mol of formaldehyde was added to 1 mol of melamine, and 100 parts of a melamine resin solution obtained by reacting at 85 ° C. for 1 hour with PH9 was added with polyethylene glycol (PEG 4000, Sanyo Kasei Co., Ltd.). Two
After adding and dispersing parts, the mixture was heated and dehydrated under reduced pressure at a vacuum degree of 100 TORR to obtain a solid modified melamine resin. Next, 70 parts of the solid modified melamine resin, 30 parts of pulp, 0.3 parts of phthalic anhydride.
Parts, zinc stearate 0.8 parts and stearic acid amide 0.2 parts were mixed, mixed, kneaded and pulverized to obtain a modified melamine resin molding material. Next, using a transfer molding machine, the molding material is subjected to a mold temperature of 145 ° C. and a molding pressure of 100 kg.
/ Cm 2 curing time was 3 minutes to obtain a molded product.
【0008】[0008]
【実施例2】実施例1のポリエチレングライコール量を
15部にした以外は実施例1と同様に処理して変性メラ
ミン樹脂成形材料、成形品を得た。Example 2 A modified melamine resin molding material and a molded product were obtained in the same manner as in Example 1 except that the amount of polyethylene glycol in Example 1 was changed to 15 parts.
【0009】[0009]
【実施例3】実施例1のポリエチレングライコール量を
30部に部にした以外は実施例1と同様に処理して変性
メラミン樹脂成形材料、成形品を得た。Example 3 A modified melamine resin molding material and a molded article were obtained in the same manner as in Example 1 except that the amount of polyethylene glycol in Example 1 was changed to 30 parts.
【0010】[0010]
【比較例】実施例1のポリエチレングライコールを用い
ない以外は実施例1と同様に処理して変性メラミン樹脂
成形材料、成形品を得た。[Comparative Example] A modified melamine resin molding material and a molded product were obtained in the same manner as in Example 1 except that the polyethylene glycol of Example 1 was not used.
【0011】実施例1乃至3と比較例の性能は、第1表
のようである。 後収縮率は成形品を110℃で7日間処理後の寸法変化
率である。The performances of Examples 1 to 3 and Comparative Example are as shown in Table 1. The post-shrinkage ratio is the dimensional change ratio after the molded product is treated at 110 ° C. for 7 days.
【0012】[0012]
【発明の効果】本発明は上述した如く構成されている。
特許請求の範囲に記載した構成を有するアミノ樹脂成形
材料においては、寸法安定性が良く、本発明の優れてい
ることを確認した。The present invention is constructed as described above.
It was confirmed that the amino resin molding material having the structure described in the claims has good dimensional stability and is excellent in the present invention.
Claims (1)
ールを添加後、減圧加熱脱水した固形アミノ樹脂を用い
たことを特徴とするアミノ樹脂成形材料。1. An amino resin molding material comprising a solid amino resin obtained by adding polyethylene glycol to an amino resin solution and then dehydrating under reduced pressure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19333691A JPH05230334A (en) | 1991-08-02 | 1991-08-02 | Amino resin molding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19333691A JPH05230334A (en) | 1991-08-02 | 1991-08-02 | Amino resin molding material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05230334A true JPH05230334A (en) | 1993-09-07 |
Family
ID=16306203
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19333691A Pending JPH05230334A (en) | 1991-08-02 | 1991-08-02 | Amino resin molding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05230334A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110615880A (en) * | 2019-09-25 | 2019-12-27 | 北京化工大学 | Epoxy compound and polyol prepolymer modified urea-formaldehyde resin and preparation method thereof |
-
1991
- 1991-08-02 JP JP19333691A patent/JPH05230334A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110615880A (en) * | 2019-09-25 | 2019-12-27 | 北京化工大学 | Epoxy compound and polyol prepolymer modified urea-formaldehyde resin and preparation method thereof |
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