JPS59141462A - Manufacture of ceramic body - Google Patents
Manufacture of ceramic bodyInfo
- Publication number
- JPS59141462A JPS59141462A JP58013420A JP1342083A JPS59141462A JP S59141462 A JPS59141462 A JP S59141462A JP 58013420 A JP58013420 A JP 58013420A JP 1342083 A JP1342083 A JP 1342083A JP S59141462 A JPS59141462 A JP S59141462A
- Authority
- JP
- Japan
- Prior art keywords
- binder
- degreasing
- ceramic body
- pores
- inorganic substance
- 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 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】
本発明はセラミックス体の製造方法に関するものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a ceramic body.
ニューセラミックスは高純度の酸化物、珪化物、炭化物
、窒化物の単独、これらの複合化合物とか、サーメット
などは代表的なものとして知られている。Typical examples of new ceramics include highly pure oxides, silicides, carbides, and nitrides, their composite compounds, and cermets.
これらのニューセラミックスの製造方法として、ドクタ
ーブレード法、押出し法、鋳込成形法、ロクロ成形法、
射出成形法等が知られている。Manufacturing methods for these new ceramics include the doctor blade method, extrusion method, cast molding method, potter's wheel molding method,
Injection molding methods and the like are known.
いずれの方法も上記の無機質は材料に粘性を付与させる
ために有機質バインダ、水、可塑剤等を添加し、加工性
を改良、向上させて製造している。In either method, the above-mentioned inorganic material is manufactured by adding an organic binder, water, a plasticizer, etc. to impart viscosity to the material, thereby improving and improving processability.
この中でも射出成形法は形状が複雑でかつ多量生産に適
していることから近年注目されたきた。Among these, injection molding has attracted attention in recent years because it produces complex shapes and is suitable for mass production.
しかし、射出条件を容易にするための有機質バインダは
セラミックス成分に対して重量比で大体12〜30%も
加えないと射出成形できないという問題がある。この有
機質バインダ:よ射出成形時には必要であるが、最終的
には有機質バインダ部を加熱除去(以後脱脂という)し
たのら焼成するため、不要なものである。However, there is a problem in that injection molding is not possible unless an organic binder is added to the ceramic component in an amount of about 12 to 30% by weight to facilitate injection conditions. This organic binder is necessary during injection molding, but is unnecessary since the organic binder portion is ultimately removed by heating (hereinafter referred to as degreasing) and then fired.
特に、有機質バインダが多くなれば多くなる稈セラミッ
クス体としてはその特性上不利となる。In particular, as the amount of organic binder increases, it becomes disadvantageous in terms of its characteristics as a culm ceramic body.
出来れば可能な限り少なくするか、又は全くない方が有
利である。しかし、現段階ではセラミックス体だけで射
出成形を行うことはできな−い。It is advantageous to have as little as possible, or none at all. However, at this stage, it is not possible to perform injection molding on ceramic bodies alone.
一般的には、セラミックス中に有機質バインダを混入し
、可塑性を与え粘性を下げ゛C射出する手段が多く用い
られている。つまり、加工性を向上さセるために有機バ
インダ、水等は欠くことのできない材料である。これら
の結合材を最終的には脱脂しなければならないため、射
出成形法ではこの脱脂方法、が最も重要な技術どなる。Generally, a method of mixing an organic binder into ceramics to impart plasticity and lower viscosity, and C-injection is often used. In other words, organic binders, water, etc. are indispensable materials for improving processability. Since these binders must ultimately be degreased, this degreasing method is the most important technique in injection molding.
一般的にはこれらのセラミックス体中の有機質バインダ
等の所謂結合材を脱脂するには緩やかに昇温しで行った
方が急速に加熱するより有利となる。しかし、緩やかに
昇温すると膨大なエネルギーと脱脂時間が必要となり、
経済的にも不利である。同時に、質入なエネルギーと時
間をかけても出来上った脱脂は完全なものではなく、脱
脂工程(特に室温から〜400°C近辺迄を1.5〜l
O”c、/Drの速度で昇温し結合材を分解除去する)
で外観の「膨れ」や「割れ」等が発生し当業界では大き
な問題となっており、解決が望まれている。Generally, in order to degrease so-called binding materials such as organic binders in these ceramic bodies, it is more advantageous to gradually raise the temperature than to rapidly heat the body. However, if the temperature is raised slowly, a huge amount of energy and degreasing time are required.
It is also economically disadvantageous. At the same time, even if we spend a lot of energy and time, the resulting degreasing is not perfect.
The temperature is increased at a rate of O”c,/Dr to decompose and remove the binder)
This is a major problem in the industry, as it causes ``bulges'' and ``cracks'' in the appearance, and a solution is desired.
本発明は、この様なセラミックス体の脱脂工程における
問題を解決するために、有機質バインダを含有するセラ
ミックス体の脱脂工程での「膨れ」「割れ」等のない樹
脂技術を提41けるものである。In order to solve such problems in the degreasing process of ceramic bodies, the present invention proposes a resin technology that does not cause "blistering" or "cracking" in the degreasing process of ceramic bodies containing organic binders. .
ずなわぢ、本発明はセラミックス微粉末に有機質バイン
ダを結合材とした混合物で成形物を形成し、該成形物の
全体または大部分を、結合材を熱分解した時の分解ガス
を吸着する細孔を有する無機物質で覆った状態で上記結
合材を加熱、脱脂するものである。In the present invention, a molded product is formed from a mixture of fine ceramic powder and an organic binder as a binder, and the entire or most part of the molded product is made of fine particles that adsorb decomposed gas when the binder is thermally decomposed. The binder is heated and degreased while covered with an inorganic substance having pores.
本発明において、特にこれらに属する無機物質として、
ゼオライトが挙げられる。ゼオライ1には天然産のもの
と合成品とがある。ゼオライトとはNa、、Caなどを
含有する含水アルミノケイ酸塩鉱物群の総称で、一般式
Me’O・A620:3・m5i02・nH2Oで示さ
れる。例えば、アナルサイト、チャバサイト、ダメリナ
イト、エリオナイ1、ナ[・ロナイト、フィリップサイ
!・、モルデナイト、ホージャサイト、クリノプヂライ
トがこの例である。これらのうち、工業的に有用なもの
はポージャサイト、モルデナイト、チャバサイト、クリ
ノプチライトである。In the present invention, particularly as inorganic substances belonging to these,
Examples include zeolite. There are two types of zeolite 1: natural products and synthetic products. Zeolite is a general term for a group of hydrous aluminosilicate minerals containing Na, Ca, etc., and is represented by the general formula Me'O.A620:3.m5i02.nH2O. For example, Anal Site, Chaba Site, Damelinite, Elionai 1, Na[ronite, Philip Sai! Examples of this are mordenite, faujasite, and clinopdilite. Among these, industrially useful ones are porgysite, mordenite, chabasite, and clinoptilite.
ゼオライ1は上記シリカ構造のSiの一部がA7!に置
換されて三次元的に発達した縮合酸を陽イオンで電気的
に中和して形成されたアルミノケイ酸塩の一種であり、
縮合型やSiとAlの比率によって若干異なるものがあ
る。規則的に配列した三次元結晶構造中には吸着の場と
なる空洞(または細孔)と、これらを連絡しふるい効果
を示ず孔路を有している。本発明者らはセラミックス体
の結合材を加熱脱脂する時に分解ガスがこの細孔に吸着
し、脱脂後の「膨れ」 「割れ」の改善に優れた効果を
発揮する新技術現象を見い出したのである。In Zeolite 1, part of the Si in the silica structure is A7! It is a type of aluminosilicate formed by electrically neutralizing a three-dimensionally developed condensed acid with a cation.
There are some differences depending on the condensed type and the ratio of Si and Al. The regularly arranged three-dimensional crystal structure has cavities (or pores) that serve as adsorption sites, and pores that connect these cavities and do not exhibit a sieving effect. The present inventors have discovered a new technological phenomenon in which decomposition gas is adsorbed into the pores when heating and degreasing the binding material of a ceramic body, which is highly effective in improving "blistering" and "cracking" after degreasing. be.
吸着は一般に、結晶構造を破壊することなく結晶水が脱
離してできたrm孔」とそれを連結する「孔路」は強い
効果を有する。その細孔は人(オンダストローム1億分
の1cm)の均一な孔径があるといわれる。In general, adsorption has a strong effect on rm pores, which are formed by desorption of crystal water without destroying the crystal structure, and pores that connect them. The pores are said to have a uniform pore diameter of a human being (1/100 millionth of a billionth of a centimeter).
セラミックス中の結合材に使用される材料又は分解分子
例えば水、H2,02、N2、CO,C。Materials used as binders in ceramics or decomposed molecules such as water, H2,02, N2, CO, C.
02等は大体2〜3人の分子径を有し、アンモニア、メ
タン、エタン、エチレン、プロパン、シクロプロパン、
プロピレン、n−ブタン、イソブタン、■−ブテン、n
−ペンタン、ベンセン、シクロヘキサン、メタノール、
酸化エチレン、フロン12、ジ−n−プロピルアミン、
パラフィン、オレフィン、等は大体4〜30人の分子径
を有する。02 etc. have a molecular diameter of approximately 2 to 3 people, and include ammonia, methane, ethane, ethylene, propane, cyclopropane,
Propylene, n-butane, isobutane, ■-butene, n
-pentane, benzene, cyclohexane, methanol,
Ethylene oxide, Freon 12, di-n-propylamine,
Paraffins, olefins, etc. generally have a molecular diameter of 4 to 30 molecules.
これらの有機物系分子を有する結合材の分解ガスが、セ
ラミックス体を製造する時の脱脂工程で無機物質に接触
すると、その無機物質の細孔部に分解ガス分子が吸着さ
れながら加熱脱脂される。その結果、「膨れ」 「割れ
」等の問題を緩和し、優れた効果を発揮するものである
。この様な効果を発揮する細孔性無機物質として、「ゼ
オライト」以外にシリカゲル、活性アルミナ、活性白土
等がある。When the decomposed gas of the binder containing these organic molecules comes into contact with an inorganic substance during the degreasing step when manufacturing a ceramic body, the decomposed gas molecules are adsorbed into the pores of the inorganic substance and are heated to be degreased. As a result, problems such as "blistering" and "cracking" are alleviated and excellent effects are achieved. Porous inorganic substances that exhibit such effects include silica gel, activated alumina, activated clay, and the like in addition to "zeolite."
本発明者らの実験ではセラミックス体を脱脂すするため
には融点、熱変形の高い材料の方が効果が大きい値が得
られた。In experiments conducted by the present inventors, it was found that a material with a high melting point and thermal deformation is more effective in degreasing a ceramic body.
さて、表1に1ゼオライト」の商品名を、表2にシリカ
ゲルの一般特性を、表3り活性アルミナの一般特性をそ
れぞれ示し、表4に活性白土の名称を示す。Now, Table 1 shows the trade name of "1 Zeolite", Table 2 shows the general properties of silica gel, Table 3 shows the general properties of activated alumina, and Table 4 shows the name of activated clay.
(以下余白) り、′に、本発明の実施例について説明する。(Margin below) Next, embodiments of the present invention will be described.
(実施f9111 )
平均粒径3 /7のΔ1203粉末100部に対しアク
ツクティクポリプロピレン(APP)65%とポリエチ
レン35%とを加え100%としたものを17部添加し
、ポソトブレンダで180 ”C30分混練後、2軸押
量機でベレット状に作成したものを試料とし゛(外径3
01m、内径101I11.、高す20非のボビン状の
成形品を射出成形により得た更に前記成形品に対して前
記第1表、第2表、第3表および第4表に示した細孔性
無機物質で前記成形品の全体又はほぼ全体が覆われる様
にして加熱脱脂した状態のものと、従来脱脂方法である
成形品をそのまま加熱炉で脱脂する方法との比較を第5
表に示す。(Practice f9111) To 100 parts of Δ1203 powder with an average particle size of 3/7, 17 parts of 65% active polypropylene (APP) and 35% polyethylene were added to make 100%, and kneaded with a Posoto blender at 180"C for 30 minutes. After that, the sample was made into a pellet shape using a twin-screw presser (outer diameter 3
01m, inner diameter 101I11. A bobbin-shaped molded article with a height of 20 cm was obtained by injection molding. The fifth section compares the molded product that has been heated and degreased so that the entire or almost the entire part is covered, and the conventional degreasing method of degreasing the molded product as it is in a heating furnace.
Shown in the table.
尚、脱脂条件と昇温スピードについては1〜b迄放冷し
たのら、成形品の脱脂状態を確認して1750℃で焼成
したものである。以下の実施例(2)乃至(4)につい
ても同様である。Regarding the degreasing conditions and temperature increase speed, the molded articles were left to cool from 1 to b, and then the molded articles were checked for degreased condition and fired at 1750°C. The same applies to Examples (2) to (4) below.
(実施例2)
平均粒径0.6μの窒化珪素(Si3Na)粉末に焼結
助剤を添加したもの100部に対しマイクロワックス、
パラフィン、αオレフィン、ポリエチレンの有機バイン
ダを組合せて180 ’Cで70〜7.000ポアズの
粘性を有する様に調整して2軸押量機でペレット状に形
成したものを試料として外径30龍、内径10mm、高
さ201のボビン状の成形品を射出成形により得た。更
に、前記成形品に対して前記第1表、第2表、第3表、
および第4表に示した細孔性無機物質で前記成形品の全
体又はほぼ全体が覆われる様にして加熱脱脂したものを
従来脱脂方法である成形品をそのまま加りツ〜炉で脱脂
する方法との比較を第6表に示す。(Example 2) Microwax,
A sample was prepared by combining an organic binder of paraffin, α-olefin, and polyethylene, adjusted to have a viscosity of 70 to 7,000 poise at 180'C, and formed into a pellet using a twin-screw extruder. A bobbin-shaped molded product having an inner diameter of 10 mm and a height of 20 mm was obtained by injection molding. Furthermore, for the molded product, the above Table 1, Table 2, Table 3,
and a conventional degreasing method in which the molded article is heated and degreased so that the entire or almost the entire molded article is covered with the porous inorganic substance shown in Table 4, and the molded article is directly degreased in a furnace. A comparison is shown in Table 6.
(以下余白)
(実施例3)
実施例(2)で得た成形物を試料とし゛C1第6表の脱
脂状態の比較結果で特に昇温条件に影響されずに良好な
結果を得た活性アルミナをベースに他の無機質材料との
組合ゼについて確認した結果が第7表および第8表であ
る。(Leaving space below) (Example 3) Using the molded product obtained in Example (2) as a sample, activated alumina obtained good results without being particularly affected by the temperature increase conditions in the comparison results of the degreased state in Table 6 of C1. Tables 7 and 8 show the results of the combination with other inorganic materials based on the above.
(以下余白)
(実施例4)
実施例(2)で得た成形物を試料として、第6表の脱脂
状態の比V結果で特に昇温条件(こ影響さね71゛に良
好な結果を得た活性アルミナをベースとし、その粒径を
増粒させ、その増粒の影響を確認し六−結果が第9表で
ある。この時活性アルミナの+IJris粒径は2〜6
μで、細孔容積は0.3〜0.67 m ff/ g
(7) モ(7)ヲ使用シ、コレを0.5 mm−12
m間迄■(71粒させプこもの、つまり個々の粒径は0
.2〜6μであるが、これを集めて0.5−〜12mm
の粒1犬Gこ調t& して船(才〜じこしたちのである
。(Leaving space below) (Example 4) Using the molded product obtained in Example (2) as a sample, the ratio V results in the degreased state in Table 6 show that good results were obtained especially under elevated temperature conditions (this effect was 71゛). Using the obtained activated alumina as a base, the particle size was increased and the effect of the increase was confirmed.The results are shown in Table 9.At this time, the +IJris particle size of the activated alumina was 2 to 6.
μ, the pore volume is 0.3-0.67 m ff/g
(7) Use Mo (7), this is 0.5 mm-12
up to m (71 grains, that is, the individual grain size is 0)
.. 2~6μ, but collect them to 0.5~12mm
The grain of the dog is G-tone T& and the ship (sai~jikoshitachino).
(以下余白)
第9表
粒径と脱脂状態
1注)実施例に用いた○△×印の記号の説明0印−20
ケ中19ケ以」二「割れ」 「膨れ」のないもの△印−
20ケ中10ケ以上「割れ」 「膨れ」のないもの×印
−20ケ中良品3ヶ以下又は全部「割れ」 「膨れ」発
生以上説明したように本発明はセラミックス微粉末に有
機質バインダを結合剤とした混合物で成形物を形成し、
該成形物の全体または大部分を無機物質で覆って加熱、
脱脂する過程において、該無機物質の構造が結合材の分
解ガスを吸着する細孔を有することを特徴としているも
のである。(Margin below) Table 9 Particle size and degreasing condition 1 Note) Explanation of the symbols ○△× used in the examples 0 mark - 20
Items with 19 or more cracks and no cracks or swelling marked with △
Out of 20 items, 10 or more had no cracks or bulges. - Out of 20 items, 3 or less were non-defective or all had cracks or bulges. As explained above, the present invention combines an organic binder with fine ceramic powder. Forming a molded article with the mixture as an agent,
Covering the entire or most part of the molded product with an inorganic substance and heating it,
In the process of degreasing, the structure of the inorganic substance is characterized by having pores that adsorb decomposition gas of the binder.
このことによってセラミックス体成形物中のバインダで
ある有負結合材を加熱脱脂する際に結合材の熱分解によ
って生ずるH 2.02、N2.1(20、及び炭化水
素系物質例えばパラフィン類、オレフィン類、ナフテン
類、アルコール類、芳香族類、アミン類、エチレン類、
プロピレン類、ブタン類等の物質が前記細孔を有する無
機物質の孔路および細孔内に吸着される。このため、脱
脂後の「膨れ」及び「割れ」の効果に大きく作用し、優
れた脱脂成形品、及び焼成品i形成するものである。こ
のことは、従来とかく長時間を要していた脱脂工程を1
0倍以上短縮するばかりでなく、成形品の焼成完成後の
良品率が大幅に向上し、関連業界に寄与することは絶大
である。As a result, H2.02, N2.1 (20), and hydrocarbon substances such as paraffins and olefins are generated by thermal decomposition of the binder when the negative binder, which is the binder in the ceramic body molded product, is heated and degreased. classes, naphthenes, alcohols, aromatics, amines, ethylenes,
Substances such as propylene and butanes are adsorbed in the pores and pores of the inorganic material having pores. Therefore, it has a large effect on the effects of "blistering" and "cracking" after degreasing, and forms excellent degreased molded products and fired products. This means that the degreasing process, which conventionally took a long time, can be reduced to one time.
Not only is the time reduced by more than 0 times, but the rate of good products after firing of molded products is greatly improved, making a tremendous contribution to related industries.
Claims (3)
した混合物で成形物を形成し、該成形物中の前記結合材
を加熱、脱脂する過程において、前記結合材の分解ガス
を吸着する細孔を有した無機物質により前記成形物の全
体または大部分を覆った伏態で前記結合材を加熱、脱脂
し、その後に焼成することを特徴としたセラミックス体
の製造方法。(1) A molded article is formed from a mixture of ceramic fine powder and an organic binder as a binder, and in the process of heating and degreasing the binder in the molded article, pores are created to adsorb decomposition gas of the binder. A method for producing a ceramic body, comprising: heating and degreasing the binder in a state where the entire or most of the molded article is covered with an inorganic substance, and then firing the binder.
解ガスの分子径とほぼ同等以上である特許811求の範
囲第1項記載のセラミックス体の製造方法。(2) The method for producing a ceramic body according to item 1 of the scope of Patent No. 811, wherein the size of the pores of the inorganic substance is approximately equal to or larger than the molecular diameter of the decomposed gas of the binder phase.
ルミナ、活性白土の微粉末または粒状のものである特許
請求の範囲第2項記載のセラミックス体の製造方法。(3) The method for producing a ceramic body according to claim 2, wherein the inorganic substance is a fine powder or granule of zeolite, silica gel, activated alumina, or activated clay.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58013420A JPS59141462A (en) | 1983-01-28 | 1983-01-28 | Manufacture of ceramic body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58013420A JPS59141462A (en) | 1983-01-28 | 1983-01-28 | Manufacture of ceramic body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59141462A true JPS59141462A (en) | 1984-08-14 |
Family
ID=11832635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58013420A Pending JPS59141462A (en) | 1983-01-28 | 1983-01-28 | Manufacture of ceramic body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59141462A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0450176A (en) * | 1990-06-18 | 1992-02-19 | Ngk Spark Plug Co Ltd | Method for defatting ceramic molding |
-
1983
- 1983-01-28 JP JP58013420A patent/JPS59141462A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0450176A (en) * | 1990-06-18 | 1992-02-19 | Ngk Spark Plug Co Ltd | Method for defatting ceramic molding |
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