JPS588753A - Amino resin molding material - Google Patents
Amino resin molding materialInfo
- Publication number
- JPS588753A JPS588753A JP10763881A JP10763881A JPS588753A JP S588753 A JPS588753 A JP S588753A JP 10763881 A JP10763881 A JP 10763881A JP 10763881 A JP10763881 A JP 10763881A JP S588753 A JPS588753 A JP S588753A
- Authority
- JP
- Japan
- Prior art keywords
- amino resin
- molding material
- resin
- resin molding
- polyester plasticizer
- 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
【発明の詳細な説明】
本発明は配線器具、電気器具等に用いられるアミノ樹脂
成形材料に関するもので、その目的とするところは成形
時の熔融粘度を低下させ成形時の高流動性を得ることに
ある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an amino resin molding material used for wiring devices, electrical appliances, etc., and its purpose is to reduce melt viscosity during molding and obtain high fluidity during molding. It is in.
従来、成形時の高流動性を得るにはパラトルエンスルホ
ン酸アミド、ポリエチレングリコール、ポリビニルアル
コール等を添加していたが、パラトルエンスルホン酸ア
ミドは添加量が多く必要でしかも効果に乏しく、ポリエ
チレングリコールやポリビニルアルコールは成形材料に
ケーキングやフロラキングを発生させる欠点があった。Conventionally, para-toluene sulfonamide, polyethylene glycol, polyvinyl alcohol, etc. were added to obtain high fluidity during molding, but para-toluene sulfonamide required a large amount to be added and was less effective. Polyvinyl alcohol and polyvinyl alcohol have the drawback of causing caking and flora in the molding material.
本発明は上記欠点を解決するもので、ポリエステル系可
塑剤を添加することによって成形時の高流動性を得るこ
とができたものである、次に本発明の詳細な説明する。The present invention solves the above-mentioned drawbacks and achieves high fluidity during molding by adding a polyester plasticizer.The present invention will now be described in detail.
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、フェノール変性メラミン樹脂等であ
り液状乃至固型状の各れでもよい。ポリエステル系可塑
剤としてはアジピン酸系ポリエステM可塑剤、七バシン
酸系ポリエステル可塑剤等のポリエステル系可塑剤全般
が用いられる。ポリエステlし系可塑剤の量は特に限定
するものでないが、好ましくは全体に対し0.5〜lO
重量%(以下単に%と記す)が望ましい。即ち0.5未
満では効果が少′なく、10%をこえると成形品外観が
低下する傾向のためである。アミノ樹脂、ポリエステル
系可塑剤以外の添加物とし゛ではアミノ樹脂成形材料と
して一般に用いられる硬化剤、離型剤、基材、充填剤、
着色剤等をそのまま用いることができ、上記材料を混合
、混練、粉砕し或は必要に応じて造粒しアミノ樹脂成形
材料を得るものである。The amino resin used in the present invention may be a urea resin, a melamine resin, a guanamine resin, a phenol-modified melamine resin, etc., and may be in either liquid or solid form. As the polyester plasticizer, general polyester plasticizers such as adipic acid polyester M plasticizer and heptabasic acid polyester plasticizer can be used. The amount of polyester plasticizer is not particularly limited, but it is preferably 0.5 to 1O based on the total amount.
Weight % (hereinafter simply referred to as %) is desirable. That is, if it is less than 0.5, the effect will be small, and if it exceeds 10%, the appearance of the molded product will tend to deteriorate. Additives other than amino resins and polyester plasticizers include curing agents, mold release agents, base materials, fillers, etc. that are commonly used as amino resin molding materials.
The coloring agent and the like can be used as they are, and the amino resin molding material can be obtained by mixing, kneading, pulverizing, or, if necessary, granulating the above materials.
以下本発明を実施例にもとすいて説明する。The present invention will be explained below using examples.
実施例1
残留水分10Φの固型メラミン樹脂60重量部(以下単
に部と記す)に対し木粉鉛部、フタル酸0.5部、ステ
アリン酸亜ff11部、着色剤1部、ポリエステル系可
塑剤(アデカアーガス化学株式会社製、アデカサイザー
PN −150) 0.5部を添加し、混線、粉砕し゛
Cメラミン樹脂成形材料を得た。Example 1 Wood powder lead, 0.5 part phthalic acid, 11 parts stearic acid ff, 1 part colorant, polyester plasticizer to 60 parts by weight (hereinafter simply referred to as parts) of solid melamine resin with residual water content of 10 Φ. (Adeka Sizer PN-150, manufactured by Adeka Argus Chemical Co., Ltd.) 0.5 part was added, mixed and crushed to obtain a C melamine resin molding material.
実施例2
樹脂含有量60%のユリア樹脂初期縮合物1800部に
対して塩化アンモニウム0,8部、水酸化す) IJウ
ム旧部、パルプ260部、ポリエステ?し系可塑剤(ア
デカアーガス化学株式会社製、アデカサイザーPN 4
00 )10部を添加し、混線、乾燥して乾燥品を得、
該乾燥品100部IC対してステアリン酸亜鉛0.5部
、着色剤0.6部を加えボールミルで着色、粉砕してア
ミノ樹脂成形材料を得た。Example 2 1800 parts of urea resin initial condensate with a resin content of 60%, 0.8 parts of ammonium chloride, hydroxide) old part of IJum, 260 parts of pulp, polyester? Plasticizer (Adeka Argus Chemical Co., Ltd., Adeka Sizer PN 4)
00), add 10 parts, cross-wire, and dry to obtain a dry product.
To 100 parts of the dry product IC, 0.5 part of zinc stearate and 0.6 part of a coloring agent were added, colored with a ball mill, and pulverized to obtain an amino resin molding material.
比較例
実施例2と同じ樹脂含有量60%のユリア樹脂初期縮合
物1800部に対して塩化アンモニウム0.8部、水酸
化ナトリウム01部、パルプ260部を添加し混合、混
線、乾燥し”C乾燥品を得、該乾燥品100部に対して
ステアリン酸亜鉛0.5部、着色剤0.5部を加えボー
ルミルで着色、粉砕してアミノ樹脂成形材料を得た。Comparative Example 0.8 parts of ammonium chloride, 01 parts of sodium hydroxide, and 260 parts of pulp were added to 1800 parts of a urea resin initial condensate with a resin content of 60% as in Example 2, mixed, mixed, and dried. A dried product was obtained, and 0.5 part of zinc stearate and 0.5 part of a coloring agent were added to 100 parts of the dry product, colored with a ball mill, and pulverized to obtain an amino resin molding material.
実施例1及び2と比較例のアミノ樹脂成形材料を成形圧
力100に4、成形温度140°Cで成形し流動性を試
験した結果は第1表に示すように本発明のアミノ樹脂成
形材料の成形時流動性はよく本発明の優れ°Cいること
を確認した。The amino resin molding materials of Examples 1 and 2 and the comparative example were molded at a molding pressure of 100°C and a molding temperature of 140°C, and the fluidity was tested. The results are shown in Table 1. It was confirmed that the fluidity during molding was superior to that of the present invention.
第 1 表 注 米円板伸び試験による。Chapter 1 Table Note: Based on rice disc elongation test.
特許出願人 松下電工株式会社 代理人弁理士 竹 元 敏 丸 (ほか2名)patent applicant Matsushita Electric Works Co., Ltd. Representative Patent Attorney Toshimaru Takemoto (2 others)
Claims (2)
とするアミノ樹脂成形材料。(1) An amino resin molding material characterized by adding a polyester plasticizer.
量%であることを特徴とする特許請求の範囲第1項記載
のアミノ樹脂成形材料。(2) The amino resin molding material according to claim 1, wherein the amount of polyester plasticizer is 0.5 to IO% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10763881A JPS588753A (en) | 1981-07-09 | 1981-07-09 | Amino resin molding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10763881A JPS588753A (en) | 1981-07-09 | 1981-07-09 | Amino resin molding material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS588753A true JPS588753A (en) | 1983-01-18 |
Family
ID=14464258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10763881A Pending JPS588753A (en) | 1981-07-09 | 1981-07-09 | Amino resin molding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS588753A (en) |
-
1981
- 1981-07-09 JP JP10763881A patent/JPS588753A/en active Pending
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