JPH03223141A - Production of artificial marble - Google Patents

Production of artificial marble

Info

Publication number
JPH03223141A
JPH03223141A JP1953490A JP1953490A JPH03223141A JP H03223141 A JPH03223141 A JP H03223141A JP 1953490 A JP1953490 A JP 1953490A JP 1953490 A JP1953490 A JP 1953490A JP H03223141 A JPH03223141 A JP H03223141A
Authority
JP
Japan
Prior art keywords
glass
synthetic resin
artificial marble
particles
particle size
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
JP1953490A
Other languages
Japanese (ja)
Inventor
Atsushi Nishino
敦 西野
Kosei Kajiwara
梶原 孝生
Kunio Kimura
邦夫 木村
Masaki Ikeda
正樹 池田
Hiroyuki Ono
博之 小野
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 Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP1953490A priority Critical patent/JPH03223141A/en
Publication of JPH03223141A publication Critical patent/JPH03223141A/en
Pending legal-status Critical Current

Links

Landscapes

  • Macromonomer-Based Addition Polymer (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the title marble, a colored composite material, easy to color, rich in color tone, ensured to be available stably at all times, by kneading a synthetic resin with glass particles surface-treated with coupling agent to effect embedding the glass particles in the synthetic resin matrix. CONSTITUTION:The surface of glass particles (0.1-10mm in size and 1.43-1.59 in refractive index) is treated with a silicon resin-based coupling agent and kneaded with a synthetic resin to effect embedding the glass particles in the synthetic resin matrix, thus obtaining the objective artificial marble. The glass, with a refractive index of 1.49-1.59, is e.g. silica glass, soda lime glass, lead alkali glass, alumina borosilicate glass, borosilicate glass, being incorporated with a colorant such as CeO2, TiO2, Se, CdS, CoO, Cr2O3, Pt, Fe, Mn or Ni.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は非晶質の着色ガラス粒子と合成樹脂とで構成さ
れた色調豊かな人工大理石製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for producing artificial marble with a rich color tone, which is composed of amorphous colored glass particles and a synthetic resin.

従来の技術 生活の多様化やオフィスの多様化により様々な建材が要
望されているが、天然の大理石は資源的に逼迫し、石材
切り出し、加工、輸送、施工等の各段階で人手を要し、
近年の建築ブームに供給が対応できない状況にある。
Conventional technology The diversification of daily life and offices has created a demand for a variety of building materials, but natural marble is a scarce resource and requires manpower at each stage of stone cutting, processing, transportation, construction, etc. ,
Supply is unable to keep up with the recent construction boom.

このような社会背景と種々のカラー化に対応するために
、人工大理石がブームになりつつある。
In order to respond to this social background and various colors, artificial marble is becoming popular.

従来の人工大理石の製造法は、マトリックスとしての樹
脂に着色顔料、着色剤を配合し、さらに天然石の様な風
合い(以下、石調柄と称する)を現出させるために天然
石粒子等をガラス繊維からなる補強材とともに樹脂に混
練して、これを成形型に注入成型していた。また他の方
法としては、樹脂に水酸化アルミニウムや水酸化カルシ
ウム等の100μm以下の超微粒子を充填材として、こ
れとガラス繊維補強材、硬化剤を加え、成形型に注入し
て石調柄を出し、さらに着色剤を部分的に塗布または挿
入したりして人工大理石を製造していた。
The conventional manufacturing method for artificial marble is to mix colored pigments and coloring agents with resin as a matrix, and to create a natural stone-like texture (hereinafter referred to as stone-like pattern), natural stone particles are mixed with glass fibers. It was mixed with a reinforcing material consisting of a resin and then injected into a mold. Another method is to use ultrafine particles of 100 μm or less such as aluminum hydroxide or calcium hydroxide as a filler in a resin, add glass fiber reinforcement and a hardening agent to the resin, and then inject it into a mold to create a stone-like pattern. Artificial marble was produced by applying or inserting coloring agents locally.

発明が解決しようとする課題 このような従来法では、色違いの人工大理石の品種を種
々設けるには樹脂を着色側割に、種々配合する必要があ
り、そのため色別に成形生産計画や工程を組まねばなら
ず、生産管理上煩雑となるなどの欠点を有していた。
Problems to be Solved by the Invention With such conventional methods, in order to produce various types of artificial marble with different colors, it is necessary to mix resin in various ways depending on the colored side. However, this method has disadvantages such as complicating production management.

さらに、着色剤、顔料等は高価であるにもかかわらず、
紫外線劣化で変色、退色したり、顔料により陰蔽力・が
異なり、大理石特有の透明感が色彩や色調等により異な
る等の問題があった。
Furthermore, although colorants and pigments are expensive,
There were problems such as discoloration and fading due to UV deterioration, shading power differing depending on the pigment, and the transparency characteristic of marble differing depending on the color and tone.

また、充填材としての水酸化アルミニウム、水酸化カル
シウム、酸化チタン等の超微粒子状粉末は1 充填材の
種類と配合量等により、最適な樹脂硬化温度が種々異な
り、多品種の製造は困難であり、かつ量産上極めて問題
である。
In addition, ultrafine particulate powders such as aluminum hydroxide, calcium hydroxide, and titanium oxide as fillers are used as fillers.1 The optimum resin curing temperature varies depending on the type and amount of filler, making it difficult to manufacture a wide variety of products. This is extremely problematic in terms of mass production.

さらに、石調柄を出す天然石(例えば石英、雲母、花崗
岩等)は産地により色調がバラツキ、または同じ産地で
もロフトによりバラツキが生じ、大きな空間用建材に用
いる場合には致命的な欠陥となる。
Furthermore, the color tone of natural stones that produce stone-like patterns (such as quartz, mica, granite, etc.) varies depending on the production area, or even from loft to loft even in the same production area, which is a fatal defect when used as a building material for large spaces.

本発明は上記課題にもとづき、着色の容易な人工大理石
の製造法を提供することを目的とする。
The present invention is based on the above-mentioned problem, and an object of the present invention is to provide a method for manufacturing artificial marble that can be easily colored.

課題を解決するための手段 本発明の特徴は、着色ガラスと合成樹脂を混練する前に
、予め着色ガラスを、カップリング剤を用いて表面処理
を施す点にある。
Means for Solving the Problems The feature of the present invention is that, before kneading the colored glass and synthetic resin, the colored glass is previously subjected to surface treatment using a coupling agent.

作用 この方法を用いることにより、色が異なったり、粒径が
異なった着色ガラスを用いても常に安定した状態で、量
産化が可能である。また、合成したガラスを用いている
ため定状的に同質のものが得られ、量産的にも有利で、
しかも長期間、色調的にも安定である さらに、このように着色ガラスの粒度を著しく大きくす
ることにより、カラー複合材の耐熱温度は、一般に20
〜30℃改善でき、樹脂の種類と着色ガラスの添加量に
も依存するが220〜250’Cの耐熱性を維持するこ
とが可能となり、システムキッチンでの耐熱限界はかな
り改善されることになる。
Effect: By using this method, even if colored glasses of different colors or particle sizes are used, mass production is always possible in a stable state. In addition, since synthetic glass is used, it is possible to obtain products of uniform shape, which is advantageous for mass production.
Moreover, the color tone is stable for a long period of time.Furthermore, by significantly increasing the particle size of the colored glass, the heat resistance temperature of the colored composite material is generally 20
It can be improved by ~30°C, and depending on the type of resin and the amount of colored glass added, it will be possible to maintain heat resistance of 220 to 250'C, which will significantly improve the heat resistance limit in system kitchens. .

実施例 本発明の実施例により詳述する。Example The present invention will be explained in detail using examples.

a)着色ガラスの組成 着色ガラスに用いる母ガラスは、石英ガラス、ソーダガ
ラス、ソーダ石灰ガラス、鉛争アルカリガラス、アルミ
ナ硼硅酸ガラス、硼硅酸ガラスなどである。着色ガラス
に用いる母ガラスの代表的な組成は、5lOa!* 、
60〜99.5vt%s  NatOハ、0.1−IG
、KaOは、o〜svt%、CaO,NgO!*+0−
13wtX1B20sj!、0〜13wt%である。
a) Composition of colored glass Mother glasses used for colored glass include quartz glass, soda glass, soda-lime glass, lead-based alkali glass, alumina borosilicate glass, and borosilicate glass. The typical composition of the mother glass used for colored glass is 5lOa! *,
60-99.5vt%s NatO, 0.1-IG
, KaO is o~svt%, CaO, NgO! *+0-
13wtX1B20sj! , 0 to 13 wt%.

また、代表的な物性は、軟化点が720”C〜1[i7
0”Cで、比重ハ2.20〜2.901 屈折率は1.
49〜1.59テ、可視部380〜780mμの透過率
は5〜100%のものが好ましい。
In addition, typical physical properties include a softening point of 720"C to 1 [i7
At 0''C, the specific gravity is 2.20-2.901 and the refractive index is 1.
49 to 1.59 Te, and the transmittance in the visible region of 380 to 780 mμ is preferably 5 to 100%.

これらの中で特に軟化点は720℃以下ではガラスの耐
熱性に影響を与えるので、これ以上のガラスを母ガラス
とする必要がある。さらに、比重は、2.1〜2.9に
あることが望ましい。この理由は、ガラスの比重が2.
9より大きいと、樹脂と混合した場合、成形体の底部に
ガラス粒子ばかりが形成されることによる。逆に、2.
1より小さい場合は表面にのみガラス粒が生成し、結合
材である樹脂が少なくなる。こうした理由から、比重は
2.1〜2.9にあることが望ましい。
Among these, especially when the softening point is 720° C. or lower, it affects the heat resistance of the glass, so it is necessary to use a glass with a softening point higher than this as the mother glass. Further, the specific gravity is preferably in the range of 2.1 to 2.9. The reason for this is that the specific gravity of glass is 2.
If it is larger than 9, only glass particles will be formed at the bottom of the molded body when mixed with resin. On the contrary, 2.
When it is smaller than 1, glass particles are generated only on the surface, and the amount of resin as a binder decreases. For these reasons, it is desirable that the specific gravity is between 2.1 and 2.9.

次に、上述した母ガラスに着色する着色剤について述べ
る。カラー発色金属イオンコロイドとして代表的なもの
を表1に示す。本発明の着色ガラスは、上述した母ガラ
スに表1に示したような着色剤を添加することによって
得ることが出来る。
Next, the coloring agent that colors the above-mentioned mother glass will be described. Table 1 shows typical color-forming metal ion colloids. The colored glass of the present invention can be obtained by adding a coloring agent as shown in Table 1 to the above-mentioned mother glass.

b)着色ガラスの粒度 従来の充填剤を構成する無機物は、2〜100μmの粒
径を有するものが一般的であるが、0.1−10a+m
の粒度を有することが着色性の観点と複合材の強度、耐
熱性の観点から好ましい。着色ガラスの粒径を0.1m
m(100μm)以下で構成すると、複合材表面でクラ
ックが発生し、クラック面で光を乱反射させるので、着
色性や石調柄出しの観点で支障をきたすので好ましくな
い。さらに、100μ−以下の超微粒子は着色ガラスの
種類により、樹脂で硬化させる際に、硬化時間や硬化程
度を変化させるので100μm以下の色ガラス粒子の添
加は好ましくない。なお、実施例では破砕粒子を用いた
が、破砕することなくガラスから直接所定形状の粒子を
得てもよい。
b) Particle size of colored glass The inorganic substances constituting conventional fillers generally have a particle size of 2 to 100 μm, but 0.1 to 10 μm
It is preferable to have a particle size of from the viewpoint of colorability and the strength and heat resistance of the composite material. The particle size of colored glass is 0.1m.
If the thickness is less than m (100 μm), cracks will occur on the surface of the composite material and light will be diffusely reflected on the cracked surface, which will cause problems in terms of colorability and stone-like patterning, which is not preferable. Further, it is not preferable to add colored glass particles of 100 .mu.m or less because ultrafine particles of 100 .mu.m or less change the curing time and degree of curing when cured with a resin depending on the type of colored glass. Although crushed particles were used in the examples, particles of a predetermined shape may be obtained directly from glass without crushing.

また、0.1〜105111の破砕粒の粒度構成は、0
.1〜10mmの範囲内で、大・中・小の粒度バランス
のとれることが重要である。しかし、目的用途により、
粒度構成を変更することも可能である。
In addition, the particle size structure of the crushed grains of 0.1 to 105111 is 0.
.. It is important to maintain a balance between large, medium, and small particle sizes within the range of 1 to 10 mm. However, depending on the intended use,
It is also possible to change the particle size configuration.

表 着色カラー C)着色ガラスの表面処理 着色ガラスの破断面の活性は、色の種類や濃度、粒度差
により様々であるため、また、使用する樹脂との接合強
度を長期間にわたり安定に保持させる目的で、シリコー
ン樹脂系のカップリング剤で予め表面処理を施した後に
樹脂と混練させる。この表面処理により、着色ガラスを
効果的に被覆するので、樹脂と硬化養生時間、硬化温度
、複合材中の気泡、複合材の美観等が、改善される。
Table Colored Color C) Surface Treatment of Colored Glass The activity of the fractured surface of colored glass varies depending on the type of color, concentration, and particle size difference, so it is important to maintain the bonding strength with the resin used stably over a long period of time. For this purpose, the surface is previously treated with a silicone resin-based coupling agent and then kneaded with a resin. Since this surface treatment effectively covers the colored glass, the resin and curing curing time, curing temperature, air bubbles in the composite material, aesthetic appearance of the composite material, etc. are improved.

d)カラー複合材用樹脂 エポキシ系、ウレタン系、アクリル系、メラミン系、フ
ェノール系、スチレン系、不飽和ポリエステル系等の種
々の樹脂を使用目的に応じて任意に選択することが可能
である。
d) Resin for color composite materials Various resins such as epoxy, urethane, acrylic, melamine, phenol, styrene, and unsaturated polyester resins can be arbitrarily selected depending on the purpose of use.

d)その他の充填材、補強材 カラー複合材を、本積のa)〜C)に記載した条件で生
産することが可能であるが、使用目的により、カラー複
合材の機械的強度を改善する目的や、カラー複合材の中
間色を調整する目的で公知のガラス繊維や一般の充填材
を一部添加することも可能である。
d) Other fillers and reinforcing materials It is possible to produce color composite materials under the conditions described in a) to C) of this article, but depending on the purpose of use, it is possible to improve the mechanical strength of the color composite material. It is also possible to partially add known glass fibers or general fillers for the purpose of adjusting the neutral color of the color composite material.

〈実施例1〉 1)不飽和ポリエステル樹脂・・20重量部2) ソー
ダ石灰ガラス(透明、粒径l〜5關、軟化点ニア30℃
、屈折率: 1.52)・・15重量部3) ソーダ石
灰ガラス(ピンク、粒径l〜5關、軟化点ニア30°C
1屈折率: 1.52、Se含有)・・5重量部4) 
ソーダ石灰ガラス、茶色、粒径l〜5mm(軟化点、屈
折率は同上、Fe、Mn含有)・・2重量部5)触媒(
日本油脂(株)製:バーメックN)・・0.2重量部 2)から5)のガラスを予め、カップリング剤(信越化
学、KBM−503)中に浸漬し表面処理を行った後、
1)から5)を混練し、混練物を型に注ぎ、60℃の養
生室で6時間、養生硬化を行ない厚み20■のカラー複
合材を得た。
<Example 1> 1) Unsaturated polyester resin...20 parts by weight 2) Soda lime glass (transparent, particle size 1-5, softening point near 30°C
, refractive index: 1.52)...15 parts by weight 3) Soda lime glass (pink, particle size l~5cm, softening point near 30°C
1 refractive index: 1.52, containing Se)...5 parts by weight4)
Soda lime glass, brown, particle size 1~5 mm (softening point, refractive index same as above, contains Fe, Mn)...2 parts by weight 5) Catalyst (
Nippon Oil & Fats Co., Ltd.: Vermec N)...0.2 parts by weight 2) to 5) glasses were previously immersed in a coupling agent (Shin-Etsu Chemical, KBM-503) for surface treatment.
1) to 5) were kneaded, and the kneaded mixture was poured into a mold and cured in a curing chamber at 60° C. for 6 hours to obtain a color composite material with a thickness of 20 cm.

〈実施例2〉 l)不飽和ポリエステル樹脂(大日本インキ化学工業(
株)製ポリライ) TP−237・・20重量部2)硼
硅酸ガラス(透明、粒径1−10+am、軟化点ニア9
5℃、屈折率: 1.49)・・15重量部3)硼硅酸
ガラス(コバルトブルー 粒径1−11−1O同上ガラ
スにCoを0.5wt%含有)・・5重量部4)硼硅酸
ガラス(茶色、粒径1−11−1O同上ガラスにFe、
Mnを1〜3wt%添加)・・5重量部5) 触媒(同
上) 2)から4)のガラスを予め、カップリング剤(信越化
学、KBM−503)中に浸漬し表面処理を行った後、
l)から5)を混練し、混練物を型に注ぎ、60℃の養
生室で5時間、養生硬化を行ない厚み20mmのカラー
複合材を得た。
<Example 2> l) Unsaturated polyester resin (Dainippon Ink & Chemicals Co., Ltd.
Polylye Co., Ltd.) TP-237...20 parts by weight 2) Borosilicate glass (transparent, particle size 1-10+am, softening point near 9)
5°C, refractive index: 1.49)...15 parts by weight 3) Borosilicate glass (cobalt blue, particle size 1-11-1O same as above glass containing 0.5 wt% Co)...5 parts by weight 4) Boron Silicate glass (brown, particle size 1-11-1O same glass as above, Fe,
Addition of 1 to 3 wt% Mn)...5 parts by weight 5) Catalyst (same as above) Glasses from 2) to 4) were previously immersed in a coupling agent (Shin-Etsu Chemical, KBM-503) and subjected to surface treatment. ,
1) to 5) were kneaded, the kneaded mixture was poured into a mold, and cured for 5 hours in a curing chamber at 60°C to obtain a color composite material with a thickness of 20 mm.

〈実施例3〉 1)25°Cで溶液粘度が1ボイスの25%メチルメタ
クリレート重合体と75%のメタクリル酸メチルよりな
るアクリルシロップ・・20重量部2) ソーダ石灰ガ
ラス(黒、粒径:l〜5IIII01  軟化点ニア3
0℃、Fe 、Mn 、Go 、Cu 、 1〜3vt
X含有)−15重量部3)触媒(過酸化ベンゾイル他)
・・0.2重量部を用意し、2)のガラスを予め、カッ
プリング剤(信越化学、KBM−503)中に浸漬し表
面処理を行った後、りから3)を混合し、上記混合物を
型に注ぎ、100℃で20分間、熱プレスして厚み20
■のカラー複合材を得た。
<Example 3> 1) Acrylic syrup consisting of 25% methyl methacrylate polymer and 75% methyl methacrylate having a solution viscosity of 1 voice at 25°C...20 parts by weight 2) Soda lime glass (black, particle size: l~5III01 Softening point near 3
0°C, Fe, Mn, Go, Cu, 1-3vt
Contains X) - 15 parts by weight 3) Catalyst (benzoyl peroxide, etc.)
・Prepare 0.2 parts by weight of glass, pre-immerse the glass in 2) in a coupling agent (Shin-Etsu Chemical, KBM-503) and perform surface treatment, then mix 3) with the above mixture. Pour into a mold and heat press at 100℃ for 20 minutes to a thickness of 20℃.
■A colored composite material was obtained.

実施例1〜3で、具体的なカラー複合材を調製したが、
天然石を用いた場合よりも色彩、石調柄、深み、光沢と
もに極めて、素晴らしい出来映えである。この表面をパ
フ研磨機で表面研磨を行なうとさらに高級感と品位が増
し、天然石とは異なるカラー複合材が得られた。
In Examples 1 to 3, specific color composite materials were prepared, but
The color, stone-like pattern, depth, and luster are far superior to those using natural stone, resulting in a wonderful workmanship. When this surface was polished using a puff polishing machine, a composite material with a color different from that of natural stone was obtained, which further increased the sense of luxury and quality.

実施例1〜3で、樹脂の代表としてアクリル系と不飽和
ポリエステル系で実施例を説明したが、その他の樹脂に
ついても同様のカラー複合材が得られた。
In Examples 1 to 3, examples were explained using an acrylic resin and an unsaturated polyester resin as representative resins, but similar color composite materials were obtained using other resins.

発明の効果 以上のように、本発明の製造法によれば、色調豊かなカ
ラー複合材を常に安定供給することが可能である。
Effects of the Invention As described above, according to the production method of the present invention, it is possible to constantly and stably supply a color composite material with rich color tone.

Claims (5)

【特許請求の範囲】[Claims] (1)合成樹脂と混練の前に、ガラスの表面をカップリ
ング剤で表面処理し、前記合成樹脂と混練して、実質的
に粒子の存在が確認可能な粒径のガラスを前記合成樹脂
から構成されるマトリックス中に埋設したことを特徴と
する人工大理石の製造法。
(1) Before kneading with the synthetic resin, the surface of the glass is treated with a coupling agent, and the glass is kneaded with the synthetic resin to obtain glass with a particle size that allows the presence of particles to be practically confirmed from the synthetic resin. A method for producing artificial marble characterized by embedding it in a matrix composed of:
(2)カップリング剤がシリコン系樹脂であることを特
徴とする請求項1記載の人工大理石の製造法。
(2) The method for producing artificial marble according to claim 1, wherein the coupling agent is a silicone resin.
(3)ガラスが、屈折率(n)1.49〜1.59の物
性を有する石英ガラス、ソーダ石灰ガラス、鉛アルカリ
ガラス、アルミナ硼硅酸ガラス、硼硅酸ガラスであり、
これに着色剤を含んでいることを特徴とする請求項1記
載の人工大理石の製造法。
(3) the glass is quartz glass, soda lime glass, lead-alkali glass, alumina borosilicate glass, or borosilicate glass having a physical property of a refractive index (n) of 1.49 to 1.59;
2. The method for producing artificial marble according to claim 1, further comprising a coloring agent.
(4)着色剤が、CeO_2、TiO_2、Se、Cd
S、CoO、Cr_2O_3、pt、Fe、Mn、Ni
であることを特徴とする請求項1または3記載の人工大
理石の製造法。
(4) Colorant is CeO_2, TiO_2, Se, Cd
S, CoO, Cr_2O_3, pt, Fe, Mn, Ni
The method for producing artificial marble according to claim 1 or 3, characterized in that:
(5)ガラス粒子が0.1〜10mmの粒径を有するこ
とを特徴とする請求項1または3記載の人工大理石の製
造法。
(5) The method for producing artificial marble according to claim 1 or 3, wherein the glass particles have a particle size of 0.1 to 10 mm.
JP1953490A 1990-01-30 1990-01-30 Production of artificial marble Pending JPH03223141A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1953490A JPH03223141A (en) 1990-01-30 1990-01-30 Production of artificial marble

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1953490A JPH03223141A (en) 1990-01-30 1990-01-30 Production of artificial marble

Publications (1)

Publication Number Publication Date
JPH03223141A true JPH03223141A (en) 1991-10-02

Family

ID=12001998

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1953490A Pending JPH03223141A (en) 1990-01-30 1990-01-30 Production of artificial marble

Country Status (1)

Country Link
JP (1) JPH03223141A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05178646A (en) * 1991-12-27 1993-07-20 Nippon Furitsuto Kk Artificial marble

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05178646A (en) * 1991-12-27 1993-07-20 Nippon Furitsuto Kk Artificial marble
JP2533261B2 (en) * 1991-12-27 1996-09-11 日本フリット株式会社 Artificial marble

Similar Documents

Publication Publication Date Title
JP3734834B2 (en) Artificial stone composition and method for producing artificial stone
AU2006346574B2 (en) Marble chip, method for preparing the same and artificial marble using the same
US11766889B2 (en) Full-body marble-patterned glass mosaic and preparation method thereof
CN103917146B (en) Engineered composite material and the product produced by which
CN101282847B (en) Synthetic stone of high translucence, method of its production and use
JP2740229B2 (en) Artificial stone and its manufacturing method
KR100441485B1 (en) Method for manufacturing artificial stone
JPH03223141A (en) Production of artificial marble
JPH02199050A (en) Artificial stone and production thereof
CN1094480C (en) Artificial stone composition and method of mfg. artificial stone
JP3688170B2 (en) Artificial stone containing waste glass
JPH02102155A (en) Production of granitic artificial stone
JPH11322392A (en) Antimicrobial artificial stone and its production
US20120177882A1 (en) Decorative Stone Compositions and Methods
JPH03223140A (en) Light-transmissible colored composite material
KR101216219B1 (en) Amorphous shape marble chip and manufacturing method thereof
JPH04280847A (en) Colored composite material
JPH03223142A (en) Colored composite material
JPH03287667A (en) Colored composite material
KR20210072972A (en) Artificial marble
JPS6362552B2 (en)
TW388749B (en) An artificial stone and a method of manufacturing therefore
JPH01203243A (en) Crystallized glassy artificial stone
JPH03159943A (en) Material for artificial marble
JP2635735B2 (en) Manufacturing method of agate-like resin article