JPS5957937A - Manufacture of calcium carbonate hardened body - Google Patents
Manufacture of calcium carbonate hardened bodyInfo
- Publication number
- JPS5957937A JPS5957937A JP57169348A JP16934882A JPS5957937A JP S5957937 A JPS5957937 A JP S5957937A JP 57169348 A JP57169348 A JP 57169348A JP 16934882 A JP16934882 A JP 16934882A JP S5957937 A JPS5957937 A JP S5957937A
- Authority
- JP
- Japan
- Prior art keywords
- particle size
- powder
- calcium carbonate
- aggregate
- pearl 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.)
- Granted
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Curing Cements, Concrete, And Artificial Stone (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】
本発明は真珠粉、サンゴ粉ないしは甲殻類の甲殻粉を原
料に用いて、装身具や室内装飾品として、あるいはタイ
ルなどの内装材として使用可能な炭酸カルシウム硬化体
を製造する方法に関する。Detailed Description of the Invention The present invention uses pearl powder, coral powder, or crustacean shell powder as raw materials to produce hardened calcium carbonate that can be used as accessories, interior decorations, or interior materials such as tiles. Regarding how to.
周知の通り、真珠やサンゴは装身具ないし室内装飾品と
して古来愛用されているが、装身具ないしは室内装飾品
に利用できILい所謂屑真珠や屑サンゴは一部が飼料、
胡粉原料、セメント配合材などとして利用されているも
のの、大部分は活用されることなく投棄されてしまうの
が通例である。甲殻類の甲殻についても同様であって、
飼料として利用される一部を除くと、殆どが投棄されて
いる。As is well known, pearls and corals have been used since ancient times as jewelry or interior decorations, but some of the so-called scrap pearls and corals that can be used for jewelry or interior decorations are used as feed,
Although it is used as a raw material for whitewash and as a cement compounding material, most of it is usually thrown away without being used. The same applies to the shells of crustaceans,
Most of it is thrown away, except for some that is used as feed.
ところが、真珠、サンゴ、甲殻類の甲殻などは、炭酸カ
ルシウムを主成分とし、その炭酸カルシウムは結晶度の
低いアラゴナイト(斜方晶系)とカルサイト(六方晶系
)であるため、化学的に合成される軽質炭酸カルシウム
(沈降炭酸カルシウム)や石灰石起源の重質炭酸カルシ
ウムに比較して、焼結しやすい性質を備えている。しか
も真珠、サンゴ、甲殻などは少量ではあるが焼結時にバ
インダーとして轡能すると考えられる有機物(キチンな
いしはコンキオリン)を含有する。これに加えて真球、
サンゴ、甲殻などけ、その粉砕物が扁平状、紡錘状など
の異方性形状をとり、焼結硬化体とするうえで優れた特
長をも有している。However, pearls, corals, crustacean shells, etc. are mainly composed of calcium carbonate, and since calcium carbonate is aragonite (orthorhombic system) and calcite (hexagonal system) with low crystallinity, chemically Compared to synthesized light calcium carbonate (precipitated calcium carbonate) and heavy calcium carbonate derived from limestone, it has the property of being easier to sinter. Moreover, pearls, corals, shells, etc., although in small amounts, contain organic substances (chitin or conchiolin) that are thought to function as binders during sintering. In addition to this, a true sphere,
Corals, shells, etc., and their crushed products take on anisotropic shapes such as flat and spindle shapes, which is an excellent feature for making sintered and hardened bodies.
本発明は真珠、サンゴ、甲殻などが具備する上記の特性
に着目し、従来は殆ど活用されていない屑真珠、屑サン
ゴないしは甲殻類の甲殻に有効利用の途を拓く炭酸カル
シウム硬化体の製造方法を提供するものであって、その
特徴とするところは5粒径が0.1μ〜105μの範囲
にある真珠粉、サンゴ粉及び甲殻類の甲殻粉から選ばれ
る粉末20〜100wt%と、粒径が500μ〜201
1011の範囲にある骨材0〜80vrt%との混合物
に、該混合物の0〜50wt%に相当する無機着色剤を
配合し、これを温度400〜1500℃で加圧成型する
ことにある。なお、本明細書に於ける粒径は、特別な断
りがない限り、平均粒径を意味する。The present invention focuses on the above-mentioned characteristics possessed by pearls, corals, shells, etc., and creates a method for producing hardened calcium carbonate that opens the door to the effective use of scrap pearls, corals, and shells of crustaceans, which have been little utilized in the past. Its characteristics include 20 to 100 wt% of powder selected from pearl powder, coral powder, and crustacean shell powder with a particle size in the range of 0.1 μ to 105 μ; is 500μ~201
The method involves blending an inorganic coloring agent corresponding to 0 to 50 wt% of the mixture into a mixture with 0 to 80 vrt% of aggregate in the range of 1011, and press-molding this at a temperature of 400 to 1500°C. Note that the particle size in this specification means an average particle size unless otherwise specified.
本発明によれば、真珠粉、サンゴ粉、甲殻粉(以下、こ
れら粉末を真珠粉などと総括する。)としては粒径0.
1μ〜105μのものが使用されるが、最終製品たる成
型体に付与丁へC:/−−−−率、密度、表面硬度に応
じて、上記の範囲内で、粒径な選択することが好ましく
、そしてこの場合、粗粒、中粒、微粒の三つのそれぞれ
の粒子径の比が約5:3:1となりているのが望ましい
。ちなみに、粗粒(粒径5−10μ)、中粒(同3〜6
μ)及び微粒(同1〜2μ)がほぼ40 : 20 :
40の重量比にある真珠粉などを使用すれば、一般に
緻密な成型体を得ることができる。According to the present invention, pearl powder, coral powder, shell powder (hereinafter, these powders are collectively referred to as pearl powder, etc.) have a particle size of 0.
A particle size of 1μ to 105μ is used, but the particle size can be selected within the above range depending on the C ratio, density, and surface hardness of the final product, which is applied to the molded product. Preferably, and in this case, the ratio of the respective three particle sizes of coarse, medium and fine particles is approximately 5:3:1. By the way, coarse grains (particle size 5-10μ), medium grains (particle size 3-6μ)
μ) and fine particles (1 to 2 μ) are approximately 40:20:
If pearl powder or the like having a weight ratio of 40 is used, a dense molded body can generally be obtained.
既述した通り、真珠粉などに元来含まれている有機物は
、焼結時にバインダーとして働くものと考えられるので
、本発明で使用する真珠粉などは焼成とか薬品処理とか
を受けていないことが好ましい。しかし、有機物を大量
に含む真珠粉などは、加圧成型時の応力分布線に有機物
の偏析が起り、放冷後の成型体に応力分布線に沿ったキ
レンが生ずる鹿れがある。従って、こうした事態が心配
される場合には、予め真珠粉などに温和な熱処理を施し
ておくことを可とする。有機物の偏析に起因するキレン
発生は、後述するような骨材を真珠粉などに混合すると
か、その混合景を増加させるとかの手段でも防止するこ
とができる。As mentioned above, it is thought that the organic substances originally contained in pearl powder etc. act as a binder during sintering, so the pearl powder etc. used in the present invention must not have been subjected to firing or chemical treatment. preferable. However, with pearl powder and the like that contain a large amount of organic matter, segregation of organic matter occurs along the stress distribution line during pressure molding, and the molded product after being left to cool tends to have cracks along the stress distribution line. Therefore, if such a situation is a concern, it is possible to subject pearl powder or the like to a mild heat treatment in advance. The occurrence of oxidation due to the segregation of organic matter can be prevented by mixing aggregate with pearl powder, etc., as described below, or by increasing the mixing ratio.
本発明の骨材はコンクリート成型体での粗骨材ないし細
骨材と同様な機能を果すものであって、これには粒径5
00μ〜20mの無機物が何れも使用可能であり、その
種類を問わない。The aggregate of the present invention performs the same function as coarse aggregate or fine aggregate in concrete moldings, and has a particle size of 5.
Any inorganic material with a diameter of 00 μm to 20 m can be used, and its type does not matter.
もつとも、前記のごとき粗粒、中粒及び微粒がほぼ40
: 20 : 40の重量比にある真珠粉などが用い
られた場合には、骨材の粒径は真珠粉などの中粒の粒径
(3〜6μ)の約ioo〜200倍の範囲にあるのが好
適であるが、仮にそれから外れたとしてもコンクリート
成型体の緻密さが幾分減少するだけのことである。しか
し、成型温度でガラス相を形成する無機物を使用すると
、概して成型後割れが生じゃすい。従って、一般忙は石
灰石、大理石などが本発明の骨材として使用される。人
造宝石なども必要に応じて骨材として使用可能である。However, the coarse grains, medium grains, and fine grains mentioned above are about 40
:20:40 weight ratio is used, the particle size of the aggregate is in the range of about ioo to 200 times the particle size (3 to 6μ) of medium particles such as pearl powder. Although it is preferable to deviate from this range, the compactness of the concrete molded body will only be reduced to some extent. However, when an inorganic material that forms a glass phase at the molding temperature is used, cracks generally occur after molding. Therefore, common materials such as limestone and marble are used as aggregates in the present invention. Artificial gemstones can also be used as aggregates if necessary.
本発明に於て骨材と真珠粉などとの混合割合は、0〜8
0重景部対100〜20重量部の範囲にあるが。In the present invention, the mixing ratio of aggregate and pearl powder etc. is 0 to 8.
It is in the range of 100 to 20 parts by weight to 0 parts by weight.
使用する骨材の粒径が大きくなればなるほど、その使用
量を減少させなければならないことはもちろんである。Of course, the larger the particle size of the aggregate used, the smaller the amount of aggregate used must be.
本発明の方法では必ずしも着色剤の使用を要件としない
けれども、必要に応じて任意の無機着色剤(無機顔料)
を使用することができる。Although the method of the present invention does not necessarily require the use of a colorant, any inorganic colorant (inorganic pigment) may be used as necessary.
can be used.
無機着色剤の使用量は、真珠粉など20〜100wt%
と骨材θ〜80wt%との混合物の50wt%以下とす
るのが適当である。The amount of inorganic coloring agent used is 20 to 100 wt% such as pearl powder.
It is appropriate that the amount is 50 wt % or less of the mixture of and aggregate θ ~ 80 wt %.
20〜100wt%の真珠粉と0〜80wt%の刊材を
混合し、必要に応じて無機着色剤を配合した混合物は、
これを400〜1500℃の温度で加圧成型することに
より、目的とする炭酸カルシウム硬化体を得ることがで
きる。成型時の圧力は100kg/d以上が好ましく、
成型時間は長いほど良いが5〜90分間程度が適してい
る。このような加圧成型はホットプレスでも実施できる
が、最も好ましいのはHIP(熱間静水圧成型)である
。A mixture of 20 to 100 wt% of pearl powder and 0 to 80 wt% of printing material, and an inorganic coloring agent added as necessary, is
By press-molding this at a temperature of 400 to 1500°C, the desired hardened calcium carbonate body can be obtained. The pressure during molding is preferably 100 kg/d or more,
The longer the molding time, the better, but approximately 5 to 90 minutes is suitable. Although such pressure molding can be carried out by hot pressing, HIP (hot isostatic pressing) is most preferable.
以上説明して来たところから明らかな通り、本発明の方
法によれば、従来は殆ど有効利用が図られていない屑真
珠、屑サンゴないしは甲殻類の甲殻から、壁掛け、置き
物などの室内装飾品、ペンダント、ブローチ、ゼクンな
どの装身具、さらにはタイルなどの内装材を製造するこ
とができる。As is clear from the above explanation, according to the method of the present invention, interior decoration items such as wall hangings and ornaments can be made from scrap pearls, coral scraps, or crustacean shells, which have not been effectively utilized in the past. It can manufacture accessories such as pendants, brooches, and zekun, as well as interior materials such as tiles.
実施例1゜
造礁サンゴをよく水洗して粉砕したサンゴ粉から粗粒(
粒径8μ)40g、中粒(粒径5μ)20g、微粒(粒
径1.5μ)40gを採取してV型ブレンダーで30分
間混合し、この混合物159を温度600℃、圧力10
00kg/iの条供下に30分間ホットプレスして直径
約40■、厚さ5−の円板状成型体を得た。この成型体
を” 1500のサンドペーパーで表面研磨して試料(
A)とした。Example 1゜Coarse particles (
40g of medium particles (particle size 8μ), 20g of medium particles (particle size 5μ), and 40g of fine particles (particle size 1.5μ) were collected and mixed in a V-type blender for 30 minutes, and this mixture 159 was heated at a temperature of 600°C and a pressure of 10%.
Hot pressing was carried out for 30 minutes under a pressure of 00 kg/i to obtain a disc-shaped molded product with a diameter of about 40 cm and a thickness of 5 cm. The surface of this molded body was polished with 1500 grit sandpaper to prepare a sample (
A).
実施例2
深海サンゴ粉(粒径8μのもの12g、5μのもの6g
、1.5μのもの12g)と2粒径750μの石灰石(
骨材)20gと、コバルトアルミナ顔料25gの混合物
を使用し、ホットプレスに代えてHIP (熱間静水圧
成型)を用いた以外は実施例1と全く同様にして試料(
B)を得た。Example 2 Deep sea coral powder (12 g of particle size 8 μ, 6 g of 5 μ
, 12g of 1.5μ) and 2 limestone (750μ) (
The sample (
B) was obtained.
実施例3
粗粒、中粒及び微粒の配合量をそれぞり、89.4g及
び8Iとした造礁サンゴ粉に粒径750μの石灰石80
gを混ぜた混合物を使用した以外は実施例1と全く同様
にして試料(C)を得た。Example 3 The blending amounts of coarse particles, medium particles, and fine particles were 89.4 g and 8I, respectively, and limestone 80 with a particle size of 750 μ was added to reef-building coral powder.
Sample (C) was obtained in exactly the same manner as in Example 1, except that a mixture of g was used.
実施例4
造礁サンゴ粉に代えて真珠粉を用いた以外は実施例1と
全く同様にして試料(D)を得た。Example 4 Sample (D) was obtained in exactly the same manner as in Example 1, except that pearl powder was used instead of reef-building coral powder.
実施例5
タラバガニの甲らをよく水洗して粉砕した粉末を用意し
、実施例1の造礁サンゴ粉に代えてこの甲ら粉末な用い
た以外は実施例1と全く同様にして試料(lを調製した
。Example 5 A powder obtained by thoroughly washing and pulverizing the carapace of a king crab was prepared, and a sample (l was prepared.
参考例
加圧成型の温度条件を600℃から350℃に変えた以
外は実施例1と同一の操作を繰返し、試料(F)を得た
。Reference Example The same operation as in Example 1 was repeated except that the temperature conditions for pressure molding were changed from 600°C to 350°C to obtain a sample (F).
次に上記の実施例及び参考例で得られた各試料を110
℃で4時間乾燥後、デシケータ−内で冷却し、吸水率、
密度、圧縮強度及びモース硬度を測定した。吸水率の測
定はJIS Z −0701に準じ、密度のIIJ定は
JIS Z −8807−76K準じて行なった。圧縮
強度は軸方向に於ける破壊荷重を断面積で除した値で表
示した。また、モース硬度はモース硬度計で測定した。Next, each sample obtained in the above Examples and Reference Examples was
After drying at ℃ for 4 hours, cooling in a desiccator, water absorption rate,
Density, compressive strength and Mohs hardness were measured. Water absorption was measured according to JIS Z-0701, and density IIJ was determined according to JIS Z-8807-76K. Compressive strength was expressed as the value obtained by dividing the fracture load in the axial direction by the cross-sectional area. Moreover, Mohs hardness was measured using a Mohs hardness meter.
測定結果を次表に示す。The measurement results are shown in the table below.
以下余白 表 1Margin below Table 1
Claims (1)
サンゴ粉及び甲殻類の甲殻粉から選ばれる粉末20〜1
00wt%と、粒径が500μ〜20wnの範囲にある
骨材O〜80wt%との混合物に、該混合物の0〜50
wt%に相当する無機着色剤を配合し、これを温度40
0〜1500℃で加圧成型することを特徴とする炭酸カ
ルシウム硬化体の製造法。 2、 前記の骨材に石灰石又は大理石を使用する特許請
求の範囲第1項記載の方法。[Claims] 1. Pearl powder having a particle size in the range of 0.1μ to 105μ;
Powder selected from coral powder and crustacean shell powder 20-1
00 wt% and 0 to 80 wt% of aggregate having a particle size in the range of 500μ to 20wn.
An inorganic coloring agent corresponding to wt% is blended, and this is heated at a temperature of 40%.
A method for producing a hardened calcium carbonate body, which comprises pressure molding at 0 to 1500°C. 2. The method according to claim 1, wherein limestone or marble is used as the aggregate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57169348A JPS5957937A (en) | 1982-09-27 | 1982-09-27 | Manufacture of calcium carbonate hardened body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57169348A JPS5957937A (en) | 1982-09-27 | 1982-09-27 | Manufacture of calcium carbonate hardened body |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5957937A true JPS5957937A (en) | 1984-04-03 |
JPS6358779B2 JPS6358779B2 (en) | 1988-11-16 |
Family
ID=15884894
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57169348A Granted JPS5957937A (en) | 1982-09-27 | 1982-09-27 | Manufacture of calcium carbonate hardened body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5957937A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011251886A (en) * | 2010-06-04 | 2011-12-15 | Inoac Corp | Method for producing calcium carbonate porous body |
CN109020456A (en) * | 2018-08-25 | 2018-12-18 | 北京建工新型建材有限责任公司 | A kind of Machine-made Sand dry-mixed mortar and preparation method thereof |
CN113200697A (en) * | 2021-05-14 | 2021-08-03 | 安徽建筑大学 | Preparation method of chemical micro-corrosion coral aggregate and geopolymer-based ultrahigh-strength coral concrete |
JP2022518306A (en) * | 2019-12-30 | 2022-03-15 | 青▲島▼理工大学 | Lightweight aggregate Ultra-high performance concrete and its preparation method |
-
1982
- 1982-09-27 JP JP57169348A patent/JPS5957937A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011251886A (en) * | 2010-06-04 | 2011-12-15 | Inoac Corp | Method for producing calcium carbonate porous body |
CN109020456A (en) * | 2018-08-25 | 2018-12-18 | 北京建工新型建材有限责任公司 | A kind of Machine-made Sand dry-mixed mortar and preparation method thereof |
JP2022518306A (en) * | 2019-12-30 | 2022-03-15 | 青▲島▼理工大学 | Lightweight aggregate Ultra-high performance concrete and its preparation method |
CN113200697A (en) * | 2021-05-14 | 2021-08-03 | 安徽建筑大学 | Preparation method of chemical micro-corrosion coral aggregate and geopolymer-based ultrahigh-strength coral concrete |
Also Published As
Publication number | Publication date |
---|---|
JPS6358779B2 (en) | 1988-11-16 |
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