JPS60251167A - Manufacture of forming material - Google Patents

Manufacture of forming material

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Publication number
JPS60251167A
JPS60251167A JP59105213A JP10521384A JPS60251167A JP S60251167 A JPS60251167 A JP S60251167A JP 59105213 A JP59105213 A JP 59105213A JP 10521384 A JP10521384 A JP 10521384A JP S60251167 A JPS60251167 A JP S60251167A
Authority
JP
Japan
Prior art keywords
molding material
manufacture
phosphoric acid
resin
melting point
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
JP59105213A
Other languages
Japanese (ja)
Inventor
岡部 秀樹
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 JP59105213A priority Critical patent/JPS60251167A/en
Publication of JPS60251167A publication Critical patent/JPS60251167A/en
Pending legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔技術分野〕 本発明はランプホルダー、ヒユーズ管、碍子基板等の電
気、電子部品やメカニカルシール、セラミックハニカム
等の機械部品やタービン、プラグ等の自動車部品に用い
ふことのできる成形材料の製造方法に関するものである
[Detailed Description of the Invention] [Technical Field] The present invention is applicable to electrical and electronic parts such as lamp holders, fuse tubes, and insulator substrates, mechanical seals, mechanical parts such as ceramic honeycombs, and automobile parts such as turbines and plugs. The present invention relates to a method for manufacturing a molding material that can be used.

〔背景技術〕[Background technology]

一般にプラスチックは、高い成形性、電気特性、耐薬品
性に優れ、又、低コストであることなど多くの特徴を有
しているが燃えやすく、有毒なガスを発生するという大
きな欠点を持っている。一方セラミックは、耐熱性、強
度、耐薬品性と優れた特性を持っているが収縮率が大き
く1寸法安定性がない。又、高圧成形、高温、長時間焼
成であルタめ、コストが高い欠点をかかえている。
In general, plastics have many characteristics such as high moldability, electrical properties, excellent chemical resistance, and low cost, but they have the major drawback of being easily flammable and emitting toxic gases. . On the other hand, ceramic has excellent properties such as heat resistance, strength, and chemical resistance, but has a large shrinkage rate and lacks one-dimensional stability. In addition, it has the disadvantage of high cost due to high pressure molding, high temperature, and long firing time.

〔発明の目的〕[Purpose of the invention]

本発明の目的とするところは従来のセラミックの有して
いる耐熱性、強度、耐薬品性を損わずに寸法精度が高く
、シかも低温、短時間で焼成可能で低コストのセラミッ
クが得られる成形材料を提供することにある。
The purpose of the present invention is to obtain a low-cost ceramic that has high dimensional accuracy without impairing the heat resistance, strength, and chemical resistance that conventional ceramics have, and that can be fired at low temperatures and in a short time. The objective is to provide a molding material that can be used.

〔発明の開示〕[Disclosure of the invention]

本発明は耐火物骨材と低融点ガラスにリン酸系バインダ
ーを添加した混合物を加熱乾燥、冷却後熱硬化性樹脂、
離型剤1着色剤等を添加したことを特徴とする成形材料
の製造方法で、以下本発明の詳細な説明す乙。
In the present invention, a mixture of refractory aggregate and low melting point glass with a phosphoric acid binder added is heated and dried, and after cooling, a thermosetting resin is added.
A detailed description of the present invention will be given below with regard to a method for producing a molding material characterized by adding a mold release agent 1 and a coloring agent.

本発明に用いる耐火物骨材としては粉末状乃至小粒状の
炭化硅素、窒化硅素、酸化硅素、酸化アルミニウム、酸
化マグネシウム、粘土質、0−石質、黒鉛等がよく単独
或は適当な組合せで用いられる。低融点ガラスとしては
軟化点350〜850℃のものがよ<、aSO℃未満で
はセラミックの耐熱性が低下し、850℃をこえると省
エネルギー性が低下するためである。リン酸系バインダ
ーとしてはリン酸、リン酸マグネシウム、メタリン酸、
ピ01Jン酸、リン酸ソーダ、リン酸アルミニウム等が
用いられ特に限定するものではない。耐火物骨材に対す
る低融点ガラスの添加量は特に限定するものではないが
好ましくは耐火物骨材20〜70重量%(以下単に俤と
記す)に対し低融点ガラス20〜70q6が望まし−。
The refractory aggregate used in the present invention is preferably silicon carbide, silicon nitride, silicon oxide, aluminum oxide, magnesium oxide, clay, stone, graphite, etc. in the form of powder or small particles, used alone or in an appropriate combination. used. The low melting point glass should preferably have a softening point of 350 to 850°C. This is because below aSO°C the heat resistance of the ceramic is reduced, and above 850°C the energy saving performance is reduced. Phosphoric acid binders include phosphoric acid, magnesium phosphate, metaphosphoric acid,
Pi-01J acid, sodium phosphate, aluminum phosphate, etc. can be used, but there are no particular limitations. The amount of low melting point glass added to the refractory aggregate is not particularly limited, but preferably 20 to 70q6 of low melting point glass to 20 to 70% by weight of the refractory aggregate (hereinafter simply referred to as 迤).

即ち耐火物骨材が20チ未満では焼成後の強度が不足し
70係をこえるとプレス成形時の不良が多発し、低融点
ガラスが2096未満では磁器化せず、70チをこえる
と収縮率が大きくなるためである。更にリン酸系バイン
ダーの量は1〜5係が好ましい。即ち1チ未満では磁器
化せず。
In other words, if the refractory aggregate is less than 20 inches, the strength after firing will be insufficient, if it exceeds 70 degrees, there will be many defects during press molding, if the low melting point glass is less than 2096 degrees, it will not become porcelain, and if it exceeds 70 degrees, the shrinkage rate will be low. This is because it becomes larger. Further, the amount of the phosphoric acid binder is preferably 1 to 5. In other words, if it is less than 1 inch, it will not become porcelain.

5チをこえるとプレス成形性が低下し吸水率が大となる
ためである。熱硬化性樹脂としてはフェノール樹脂、メ
ラミン樹脂、不飽和ポリエステル樹脂、フラン樹脂、ジ
アリルフタレート樹脂、エポキシ樹脂、ユリア樹脂等の
熱硬化性樹脂全般を用いることができるが好ましくは硬
化反応過程で気体や液体等の反応副生成物を発生しない
エポキシ樹脂、不飽和ポリエステV゛樹脂、ジアリルフ
タレート樹脂等を5〜20チ用いることが望ましい、即
ち5チ未満ではプレス成形性が低下し、20 q6をこ
えふと脱脂に長時間要し省エネルギーにならないためで
ある。離型剤としてはアマイド、ポリエチレン等を用い
ることができ1〜5係添加することが好ましい。即ち1
チ未満では混練時の混線機への付着性か大となり、5係
をこえると脱脂に長時間を要するためである0着色剤と
してはベンガラ、クロムチタンイエロー、酸化チタン、
酸化コバルト等を用い為ことかでき種類、添加量共に特
に限定するものではないが好ましくは耐熱性のある無機
顔料を2− to %添加することが望ましい。即ち2
チ未満では均一着色性が低下し、lo gAをこえると
強度が低下するためである。更に必要に応じて水、アル
コール等の分散剤を加えることができるが好ましくは1
−5係が望ましい。即ち1チ未満では分散性が低下し、
5チをこえふと加熱乾燥に長時間要するためである。混
合順序は特に限定す石ものではないが、好ましくは耐火
物骨材、低融点ガラス、着色剤の混合物に対しリン酸系
バインダーを添加するが、この際リン酸系バインダーの
粘度、分散程度によっては予じめリン酸系バインダーに
分散剤を加えリン酸系バインダーの粘度を希釈調整して
おくこともできる。次に上記混合物をZoo −150
℃で3〜5時間加熱乾燥した後。
This is because if it exceeds 5 inches, the press formability will decrease and the water absorption rate will increase. As the thermosetting resin, general thermosetting resins such as phenol resin, melamine resin, unsaturated polyester resin, furan resin, diallyl phthalate resin, epoxy resin, and urea resin can be used, but it is preferable that gas or It is desirable to use epoxy resin, unsaturated polyester resin, diallyl phthalate resin, etc., which does not generate reaction by-products such as liquid, from 5 to 20 inches. This is because degreasing takes a long time and does not save energy. As the mold release agent, amide, polyethylene, etc. can be used, and it is preferable to add 1 to 5 parts. That is, 1
If it is less than 5%, it will stick to the mixing machine during kneading, and if it is more than 5%, it will take a long time to degrease.
Since cobalt oxide or the like can be used, the type and amount added are not particularly limited, but it is preferable to add 2 to % of a heat-resistant inorganic pigment. That is, 2
This is because if it is less than 1, the uniform coloring property will decrease, and if it exceeds logA, the strength will decrease. Furthermore, a dispersant such as water or alcohol can be added as necessary, but preferably 1
-5 section is desirable. That is, if it is less than 1 inch, the dispersibility decreases,
This is because heating and drying takes a long time, exceeding 5 inches. Although the mixing order is not particularly limited, it is preferable to add the phosphoric acid binder to the mixture of the refractory aggregate, low melting point glass, and colorant. Alternatively, a dispersant may be added to the phosphoric acid binder in advance to dilute and adjust the viscosity of the phosphoric acid binder. Next, the above mixture was added to Zoo-150
After heating and drying at ℃ for 3 to 5 hours.

室温迄冷却してから熱硬化性樹脂、離型剤を添加し、ロ
ール、ニーダ−等の混線機で混練した後。
After cooling to room temperature, a thermosetting resin and a mold release agent are added, and the mixture is kneaded using a mixer such as a roll or a kneader.

ナラ式粉砕機、カッターミル、フェザ−ミル等で粉砕し
て成形材料を得るものである。成形材料は通常の成形方
法で成形し成形品を得、次に焼成してセラミックとすみ
ものである。
The molding material is obtained by pulverizing with an oak type pulverizer, cutter mill, feather mill, etc. The molding material is molded by a normal molding method to obtain a molded product, and then fired to produce ceramic and sumimono.

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乃至3 第1表の配合表に基き材料を配合、混合、混線粉砕して
成形材料を得た。
Examples 1 to 3 Molding materials were obtained by blending, mixing, and cross-grinding the materials based on the recipe shown in Table 1.

第 1 表 係 〔発明の効果〕 実施例1乃至3の成形材料を成形圧力200VJcd、
160℃で3分間圧縮成形して得た成形品を200℃で
30分、400℃で90分、600℃で120分焼成し
て得たセラミックと普通の磁器を従来例として比較した
結果は第2表で明白なように本発明のセラミツクの性能
はよく本発明の優れていることを確認した
Table 1 [Effect of the invention] The molding materials of Examples 1 to 3 were molded at a molding pressure of 200 VJcd.
The results of comparing conventional ceramics obtained by compression molding at 160°C for 3 minutes and firing them at 200°C for 30 minutes, 400°C for 90 minutes, and 600°C for 120 minutes as conventional examples are as follows. As is clear from Table 2, the performance of the ceramic of the present invention was well confirmed to be superior to that of the present invention.

Claims (2)

【特許請求の範囲】[Claims] (1)耐火物骨材と低融点ガラスにリン酸系バインダー
を添加した混合物を加熱乾燥、冷却後熱硬化性樹脂、離
型剤、着色剤等を添加したことを特徴とする成形材料の
製造方法。
(1) Manufacture of a molding material characterized by heating and drying a mixture of refractory aggregate and low-melting point glass with a phosphoric acid binder added thereto, and adding a thermosetting resin, a mold release agent, a coloring agent, etc. after cooling. Method.
(2)熱硬化性樹脂が硬化反応過程で気体や液体等の反
応副生成物を発生しないものであることを特徴とする特
許請求の範囲第1項記載の成形材料の製造方法。
(2) The method for producing a molding material according to claim 1, wherein the thermosetting resin does not generate reaction by-products such as gas or liquid during the curing reaction process.
JP59105213A 1984-05-24 1984-05-24 Manufacture of forming material Pending JPS60251167A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59105213A JPS60251167A (en) 1984-05-24 1984-05-24 Manufacture of forming material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59105213A JPS60251167A (en) 1984-05-24 1984-05-24 Manufacture of forming material

Publications (1)

Publication Number Publication Date
JPS60251167A true JPS60251167A (en) 1985-12-11

Family

ID=14401386

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59105213A Pending JPS60251167A (en) 1984-05-24 1984-05-24 Manufacture of forming material

Country Status (1)

Country Link
JP (1) JPS60251167A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4898701A (en) * 1987-01-23 1990-02-06 T&N Materials Research Limited Manufacture of shaped articles from refractory powder

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4898701A (en) * 1987-01-23 1990-02-06 T&N Materials Research Limited Manufacture of shaped articles from refractory powder

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