JPH03164482A - Production of ceramic porous body - Google Patents
Production of ceramic porous bodyInfo
- Publication number
- JPH03164482A JPH03164482A JP30353789A JP30353789A JPH03164482A JP H03164482 A JPH03164482 A JP H03164482A JP 30353789 A JP30353789 A JP 30353789A JP 30353789 A JP30353789 A JP 30353789A JP H03164482 A JPH03164482 A JP H03164482A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- powder material
- porous
- particle size
- ceramic powder
- 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
- 239000000919 ceramic Substances 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000000843 powder Substances 0.000 claims abstract description 38
- 239000002245 particle Substances 0.000 claims abstract description 12
- 238000005245 sintering Methods 0.000 claims abstract description 10
- 238000002156 mixing Methods 0.000 claims abstract description 9
- 238000000465 moulding Methods 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 239000000463 material Substances 0.000 claims description 26
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052751 metal Inorganic materials 0.000 abstract description 4
- 239000002184 metal Substances 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 4
- 238000000354 decomposition reaction Methods 0.000 abstract description 2
- 230000007850 degeneration Effects 0.000 abstract 1
- 239000011148 porous material Substances 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 5
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 238000007639 printing Methods 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はセラミックス多孔質体の製造方法に関するもの
で、多孔質印字体、多孔質印字輪、多孔質ローラー、ス
タンプパッド等に利用できるものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a porous ceramic body, which can be used for porous printed bodies, porous printing wheels, porous rollers, stamp pads, and the like.
従来、多孔質印字体、多孔質印字輪、多孔質ローラー、
スタンプパッド等の多孔質のインキ含浸体には、(イ)
合成樹脂(ロ)合成ゴム(ハ)繊維、フェルト(ニ)金
属等を使用し、前述の各種多孔質体に利用されてきたか
、以下の欠点があった。(イ)合成樹脂製については、
含浸されるインキによって浸される場合があること。(
ロ)合成ゴムの場合は、“ゴム”の特性である弾性か。Conventionally, porous printing bodies, porous printing wheels, porous rollers,
For porous ink-impregnated bodies such as stamp pads, (a)
Synthetic resins (b), synthetic rubber (c) fibers, felt (d) metals, etc. have been used in the various porous bodies mentioned above, but they have the following drawbacks. (a) For synthetic resin products,
That it may be soaked by the ink being impregnated. (
b) In the case of synthetic rubber, is it elasticity, which is a characteristic of "rubber"?
インキによって失われてしまう場合かあること。It may be lost due to ink.
(ハ)繊維、フェルトの場合は、文字等の印面を形成し
がなく、鮮明捺印ができない、(ニ)金属の場合は、金
属の酸化によるインキの変質を防止できないこと。以上
のように、すべて一長一短があり、多孔質体として必要
な条件としてインキに浸されないこと、また、インキを
変質させないこと、多孔質体が常温にて変質しない安定
なものであること等、未だに満足できるものが得られて
いない0本出願はこれらの欠点をすべて解決し、安価な
多孔質体を提供するものである。(c) In the case of fibers and felt, it is impossible to form a stamp surface with characters, etc., making it impossible to print clearly. (d) In the case of metal, deterioration of the ink due to oxidation of the metal cannot be prevented. As mentioned above, all of them have advantages and disadvantages, and the necessary conditions for porous materials include not being immersed in ink, not changing the quality of the ink, and ensuring that the porous material is stable and does not change at room temperature. The present application solves all of these drawbacks and provides an inexpensive porous body.
前述の問題を解決するために、セラミックス粉末を使用
し多孔質体をIjA造するもので、粒径0.1μ〜10
)tのセラミックス粉末材(A)と該粉末材(A)の焼
結温度までで分解する粒径10μ〜100μの粉末材(
B)とを混合し造粒して、該混合造粒粉末を金型にて成
型後加熱焼結させることを特徴とするセラミックス多孔
質体の製造方法。In order to solve the above-mentioned problem, a porous body is made using ceramic powder, and the particle size is 0.1 μ to 10 μm.
) T ceramic powder material (A) and a powder material (A) with a particle size of 10 μ to 100 μ that decomposes up to the sintering temperature of the powder material (A)
A method for producing a ceramic porous body, which comprises mixing and granulating B), molding the mixed granulated powder in a mold, and then heating and sintering it.
以下実施例にて説明する。This will be explained below using examples.
第1図は、製造工程図であり、セラミックス粉末材(Δ
)はR径0.1μ〜10μの範囲で該成分としては、ア
ルミナ、ジルコニア、酸化ケイ素、酸化チタン、炭化ケ
イ素、窒化ケイ素等がある。Figure 1 is a manufacturing process diagram, and shows the ceramic powder material (Δ
) has an R diameter in the range of 0.1 μm to 10 μm, and the components include alumina, zirconia, silicon oxide, titanium oxide, silicon carbide, silicon nitride, etc.
次に、前述のセラミックス粉末材(A)より分解温度か
低く、かつ常温では粉末である物質であって、粒径10
μ〜100μのもので、例えば、バレイショデンプン、
ポリエチレン、塩化ビニル、アクリル等かある。Next, a substance that has a lower decomposition temperature than the ceramic powder material (A) described above and is a powder at room temperature, and has a particle size of 10
μ to 100μ, such as potato starch,
There are polyethylene, vinyl chloride, acrylic, etc.
さて、セラミックス粉末材(A)と分解する粉末材(B
)とを、70:30〜30 : 70の比率にて混合機
により充分混合する。この混合比率により多孔質体の気
孔率を決定できるのであり、混合比率が70:30以下
では連続気孔ができなく、また、3070以上では多孔
質体の硬さ、もろさ、ひずみ等が大きくなり、使用に耐
えられない。Now, the ceramic powder material (A) and the decomposing powder material (B)
) in a mixer at a ratio of 70:30 to 30:70. The porosity of the porous material can be determined by this mixing ratio; if the mixing ratio is less than 70:30, continuous pores will not be formed, and if it is more than 3070, the hardness, brittleness, distortion, etc. of the porous material will increase. It cannot withstand use.
この混合粉末を常温にて、金型に一定凰充填後1000
〜2,000 kg/ aJ1程の圧力にて成型する。After filling this mixed powder into a mold at a certain temperature at room temperature,
Molding is performed at a pressure of ~2,000 kg/aJ1.
セラミックス粉末材(A>の組成、またはセラミックス
粉末材<A)と分解する粉末材(B)との混合比率によ
っては、成型しに<<、型くずれを発生ずる場合がある
ので、成型のために、ワックス、熱可塑性樹脂、熱硬化
性樹脂、セルロース等の一次成型用のためのバインダー
を使用する。Depending on the composition of the ceramic powder material (A) or the mixing ratio of the ceramic powder material <A> and the decomposing powder material (B), deformation may occur during molding. , wax, thermoplastic resin, thermosetting resin, cellulose, etc. are used as binders for primary molding.
次に、焼結炉にて昇温、焼結させる。Next, the temperature is raised and sintered in a sintering furnace.
実施例1
セラミックス粉末材(A>アルミナ粒径0.1μ〜10
μを 100重社部と、バレイシラデンプン100重社
部とを、混合撹拌機にて充分混合し、造粒機にてバイン
ダー2平旦部と共に造粒した後、文字凹型をいれた金型
に1重置部計撤し、充填後油圧プレスで2,000 k
g/cdの圧力にて1分間常温にて加圧保持し、第2図
に示す一次成型後の印字体を得る。この成型後の印字体
を脱脂工程として室温〜600℃まで10℃/時の昇温
を行い、次に焼結として600〜1,400℃を2℃/
分昇温で行い、冷却し、多孔質印字体を得た。この多孔
質印字体(2の気孔率は約50%、気孔径10μ〜10
0μであった。Example 1 Ceramic powder material (A>Alumina particle size 0.1μ to 10
After thoroughly mixing μ with 100 parts of barley silla starch and 100 parts of barley silla starch with a mixer and granulating it with 2 parts of binder in a granulator, it was put into a mold with concave letters. 2,000 k by hydraulic press after removing 1 stack and filling
The pressure is maintained at room temperature for 1 minute at a pressure of g/cd to obtain a printed body after primary molding as shown in FIG. This molded printed body is degreased by increasing the temperature from room temperature to 600°C by 10°C/hour, and then sintering from 600 to 1,400°C by 2°C/hour.
The temperature was raised for 1 minute, and then cooled to obtain a porous printed body. This porous printed body (the porosity of 2 is approximately 50%, the pore diameter is 10 μ to 10
It was 0μ.
実施例2
セラミックス粉末材(A)ジルコニア粒径0.1μ〜・
10μを 100重斑部と、焼失する粉末材(B)とし
て粒径10μ〜100μのポリエチレンを80重量部、
及びバインターとしてワックス10重量部を使用し、造
粒機にて造粒して、第71図に示す円柱状の成型金型に
100重足部計1し、充填後油圧プレスで、圧力2,0
00 k+r/ cd、時間1分にて第71図の一次成
型物を得た0次に、焼結炉にて、脱脂を室温〜600″
Cまで昇温10℃/時行い、焼結を600〜1.500
″C1昇温10℃/分行い、冷却し、多孔質ローラーを
得た。この多孔質ローラーの気孔率は約50%で気孔径
10μ〜80μであった。Example 2 Ceramic powder material (A) Zirconia particle size 0.1μ~・
10μ of polyethylene with a particle size of 10μ to 100μ as a powder material (B) to be burned out, 80 parts by weight,
Using 10 parts by weight of wax as a binder, granulate it with a granulator, place it in a cylindrical mold shown in Fig. 71 in total of 100 parts by weight, and after filling, use a hydraulic press to press 2, 0
00 k+r/cd, time 1 minute to obtain the primary molded product shown in Figure 71. Next, degreasing was performed in a sintering furnace at room temperature to 600".
The temperature is increased to 10℃/hour to 600 to 1.500℃, and the sintering is
"C1 temperature was raised at 10° C./min and cooled to obtain a porous roller. The porous roller had a porosity of about 50% and a pore diameter of 10 μm to 80 μm.
実施例3
アルミナ粒径0.1μ〜10μのセラミックス粉末材(
A) 100重量部と、焼失する粉末材(B)として
、粒径10μ〜100μの塩化ビニルを 120重量部
、及びバインダーとしてアクリルを10重1部を使用し
、造粒機にて造粒し、第3図(ロ)に示ず凸盤用の凹型
に厚さ 1m/mで均一にした後、セラミックス粉末材
(A)のみを積層させ、油圧プレスで圧力2,000
ktx/cd、時間1分にて成型する。Example 3 Ceramic powder material with alumina particle size of 0.1 μm to 10 μm (
A) 100 parts by weight, 120 parts by weight of vinyl chloride with a particle size of 10μ to 100μ as the powder material (B) to be burnt out, and 1 part by weight of acrylic as a binder, and granulated with a granulator. , After making the concave mold for the convex plate uniform in thickness at 1 m/m (not shown in Fig. 3 (b)), only the ceramic powder material (A) was layered, and the pressure was set at 2,000 with a hydraulic press.
Mold at ktx/cd for 1 minute.
この−次成型品は、第3図(ロ)に示す通り表面層の厚
さ 0.3m/m〜L7m/mのみ分解する粉末材(8
1が°混合されている。これを焼結炉にて脱脂として室
温〜600℃、昇温10℃/時、焼結として600〜1
,400℃、昇温10℃/分を行い、冷却すると表面層
のみ多孔質体である印字体が得られた。該印字体をホル
ダー(3)に取付け、第3図(イ)の印字軸とした。As shown in Figure 3 (b), this second molded product is made of a powder material (8.0
1 is mixed. This is degreased in a sintering furnace at room temperature to 600℃, heated at 10℃/hour, and sintered to 600 to 1
, 400° C., and heating at 10° C./min, and when cooled, a printed material was obtained in which only the surface layer was porous. The printed body was attached to a holder (3) and used as a printing shaft as shown in FIG. 3(A).
実施例4
実施例1に示すセラミックス粉末材(A>と分解する粉
末材(B)との、混合しバインダーと共に造粒した粉末
を金型に充填し、油圧プレスで圧力2 、000kIr
/ aJ、時間1分にて、成型物として厚さ10m/m
、大きさ50m / m X 120m / mの板状
のものを得た。これを脱脂として室温〜600 ’Cま
で昇温10℃/時、焼結として600〜1,400°C
まで昇温10°C/分で焼結して、冷却後水性インキを
含浸させ、第5図に示すスタンプ台とした。Example 4 The ceramic powder material (A> shown in Example 1) and the decomposable powder material (B) were mixed and granulated together with a binder, and a mold was filled with the powder and the mixture was heated to a pressure of 2,000 kIr using a hydraulic press.
/ aJ, time 1 minute, thickness 10m/m as a molded product
A plate-like piece with a size of 50 m/m x 120 m/m was obtained. This is degreased and heated at 10°C/hour from room temperature to 600'C, and sintered at 600-1,400°C.
The stamp pad was sintered at a temperature increase of 10° C./min until the stamp was cooled, and then impregnated with water-based ink to form the stamp pad shown in FIG.
以上の通り、セラミックス粉末材(A>と分解焼失する
粉末材(B)とを混合、造粒した粉末を成型後焼結した
多孔質体は、印字体、印字軸、ローラー、スタンプパッ
ド等に使用すると、■混合比重、粉末材(A)の成分の
変化により、気孔率、硬さ等が任意に変えることができ
るので使用目的にあったものを製造できる。■インキと
の反応性は乏しいので、インキの変質及び多孔質体の老
化か殆どない。As mentioned above, the porous body obtained by mixing and granulating the ceramic powder material (A) and the powder material (B) that decomposes and burns out is molded and sintered. When used, ■Porosity, hardness, etc. can be changed arbitrarily by changing the mixing specific gravity and the components of the powder material (A), so it can be manufactured to suit the purpose of use. ■Poor reactivity with ink. Therefore, there is almost no deterioration of the ink or aging of the porous material.
第1図 製 造 工 程 図
第2図 実施例1の斜視図
第3図(イ) 実施例3の斜視図
u (ロ) n の印字体図第4図
実施例2の斜視図
第5図 実施例4の斜視図
■ =
印
而
2 :
印
字
体
3 :
ホルダーFig. 1 Manufacturing process Fig. 2 Perspective view of Example 1 Fig. 3 (A) Perspective view of Example 3 U (B) Printed image of n Fig. 4
Perspective view of Embodiment 2 Figure 5 Perspective view of Embodiment 4 ■ = Imprint 2: Print body 3: Holder
Claims (1)
粉末材(A)の焼結温度までで分解する粒径10μ〜1
00μの粉末材(B)とを混合し造粒して、該混合造粒
粉末を金型にて成型後加熱焼結させることを特徴とする
セラミックス多孔質体の製造方法。Ceramic powder material (A) with a particle size of 0.1 μ to 10 μ and a particle size of 10 μ to 1 that decomposes up to the sintering temperature of the powder material (A)
A method for producing a ceramic porous body, which comprises mixing and granulating a powder material (B) of 00 μm, molding the mixed granulated powder in a mold, and then heating and sintering it.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30353789A JPH03164482A (en) | 1989-11-22 | 1989-11-22 | Production of ceramic porous body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30353789A JPH03164482A (en) | 1989-11-22 | 1989-11-22 | Production of ceramic porous body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03164482A true JPH03164482A (en) | 1991-07-16 |
Family
ID=17922188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30353789A Pending JPH03164482A (en) | 1989-11-22 | 1989-11-22 | Production of ceramic porous body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03164482A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61281082A (en) * | 1985-06-06 | 1986-12-11 | 東陶機器株式会社 | Manufacture of porous ceramics |
JPS6472979A (en) * | 1987-09-14 | 1989-03-17 | Kubota Ltd | Production of porous ceramics |
JPH0269367A (en) * | 1988-09-05 | 1990-03-08 | Showa Denko Kk | Granule for molding ceramic porous sintered compact |
-
1989
- 1989-11-22 JP JP30353789A patent/JPH03164482A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61281082A (en) * | 1985-06-06 | 1986-12-11 | 東陶機器株式会社 | Manufacture of porous ceramics |
JPS6472979A (en) * | 1987-09-14 | 1989-03-17 | Kubota Ltd | Production of porous ceramics |
JPH0269367A (en) * | 1988-09-05 | 1990-03-08 | Showa Denko Kk | Granule for molding ceramic porous sintered compact |
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