JPS6144747A - Manufacture of artificial marble - Google Patents
Manufacture of artificial marbleInfo
- Publication number
- JPS6144747A JPS6144747A JP59158188A JP15818884A JPS6144747A JP S6144747 A JPS6144747 A JP S6144747A JP 59158188 A JP59158188 A JP 59158188A JP 15818884 A JP15818884 A JP 15818884A JP S6144747 A JPS6144747 A JP S6144747A
- Authority
- JP
- Japan
- Prior art keywords
- filler
- artificial marble
- particle size
- add
- wear resistance
- 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
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】
〔産業上の利用分野〕
本発明は、粒径の小さい充填材を用いることにより耐摩
耗性に優れた人造大理石を得ることのできる製造方法に
関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a manufacturing method that makes it possible to obtain artificial marble with excellent wear resistance by using a filler with a small particle size.
尚、ここでいう人造大理石とは、天然大理石に類似の外
観と用途を有する人工的な製品のことである(以下、同
じ)。Note that the term "artificial marble" as used herein refers to an artificial product that has an appearance and use similar to natural marble (the same applies hereinafter).
従来にあって、この種の人造大理石を製造する方法には
、レジンコンクリートによる場合があり、耐摩耗性を上
げる方法としてハードコートによる場合、ゲルコート層
を形成する場合等がある。Conventionally, methods for manufacturing this type of artificial marble include using resin concrete, and methods for increasing wear resistance include using hard coating and forming a gel coat layer.
レジンコンクリートの場合は、通常、プレポリマーに重
合開始剤、充填材及び添加材を加え、これを充分に混練
し、真空脱気することでスラリー状混合物を得ている。In the case of resin concrete, a slurry-like mixture is usually obtained by adding a polymerization initiator, filler, and additives to a prepolymer, thoroughly kneading the mixture, and vacuum degassing.
この場合にあって、充填材の粒径は数μm〜0.5額と
かなり大きなものである。そして、該スラリー状混合物
を型に流し込み、室温に静置し或いは室温以上で加熱す
ることで硬化させ、切削加工、加熱による曲げ加工、張
り合わせ9表面仕上等を行い、厨房或いは浴室のカウン
タートップ、テーブル、内外装材、浴槽等の製品として
用いている。In this case, the particle size of the filler is quite large, ranging from several μm to 0.5 μm. Then, the slurry mixture is poured into a mold, left to stand at room temperature or cured by heating above room temperature, and subjected to cutting, bending by heating, lamination 9 surface finishing, etc., to create a countertop for a kitchen or bathroom. It is used for products such as tables, interior and exterior materials, and bathtubs.
ハードコートの場合は、プラスチック表面に必要に応じ
てプレコートを施した後、ディップコート、スプレーコ
ート、フローコート等の技術によりオルガノシラン系、
多官能アクリル系等のハードコート剤を溶剤で希釈して
塗布している。そして、これを乾燥させて溶剤の除去を
行い、熱処理或いは紫外線照射等により硬化させている
。In the case of hard coating, after pre-coating the plastic surface as necessary, organosilane-based,
A hard coating agent such as polyfunctional acrylic is diluted with a solvent and applied. This is then dried to remove the solvent, and cured by heat treatment, ultraviolet irradiation, or the like.
ゲルコート層は、レジンコンクリートあるいはFRP成
形品等の美観と保護を目的として行うもので、例えばポ
リエステル樹脂ではイソフタル酸系のものが使用されて
いる。成形方法は、型の表面にガラス繊維を含まない樹
脂N(充填材は添加する)を形成し、そのゲル化を待っ
て所定の積層を行い、製品としている。このゲルコート
層を形成した製品は、耐水性、耐薬品性及び機械的強度
に優れている。The gel coat layer is applied for the purpose of aesthetics and protection of resin concrete or FRP molded products, and for example, isophthalic acid-based polyester resins are used. The molding method is to form a resin N that does not contain glass fibers (filler is added) on the surface of a mold, wait for it to gel, and then perform predetermined lamination to produce a product. Products formed with this gel coat layer have excellent water resistance, chemical resistance, and mechanical strength.
(発明が解決しようとする問題点〕
ところが、前記従来のレジンコンクリートの場合は、充
填材として数μ−〜0.5 vaの比較的粗い粒径の無
機粉体を使用している。それで、硬化した樹脂と該充填
材との密着が弱く、引っかき、摩耗等により充填材が脱
離するという欠点があった。(Problems to be Solved by the Invention) However, in the case of the conventional resin concrete, an inorganic powder with a relatively coarse particle size of several microns to 0.5 va is used as a filler. There is a drawback that the adhesiveness between the cured resin and the filler is weak, and the filler comes off due to scratching, abrasion, etc.
そのため、レジンコンクリートの表面に、更にハードコ
ート、ゲルコート層等を形成しているのが現状であり、
工程が複雑化し、またコストアンプの原因になっていた
。Therefore, the current situation is to further form a hard coat, gel coat layer, etc. on the surface of resin concrete.
This made the process complicated and also caused an increase in costs.
またハードコートの場合は、処理工程が多いという欠点
がある。しかもハードコート剤をプラスチック表面に塗
布した後は、クランク等が発生しないように温度・湿度
等を空調設備により調節して徐々に溶剤を除去しなけれ
ばならず、温度・湿度の管理が面倒である。またそのた
めの設備も大損りとなる欠点があった。それに、ハード
コート剤の特性から該ハードコート剤の膜厚が限定され
、3〜8μ−の極めて薄いものしか得られず、硬度や強
度が不足するという欠点があった。更に、基材としての
プラスチック材料とハードコート剤との接着力は、限ら
れた組合せでないと充分でなく、剥離が起こり易いとい
う欠点があった。Further, in the case of a hard coat, there is a drawback that there are many processing steps. Moreover, after applying the hard coat agent to the plastic surface, the temperature and humidity must be adjusted using air conditioning equipment to prevent the occurrence of cranks, etc., and the solvent must be gradually removed, making temperature and humidity control troublesome. be. Moreover, the equipment for this purpose also had the disadvantage of being a major loss. In addition, the film thickness of the hard coating agent is limited due to the characteristics of the hard coating agent, and only an extremely thin layer of 3 to 8 .mu.m can be obtained, resulting in insufficient hardness and strength. Furthermore, the adhesive force between the plastic material as the base material and the hard coating agent is insufficient unless the combination is limited, and there is a drawback that peeling is likely to occur.
更に、ゲルコート層を形成する場合は、ゲルコート層の
ゲル化後に所定の積層を行っており、成形工程が繁雑で
ある。特に、注型品の場合は一度の成形でゲルコート層
を付与するのが困難であり、また基材との接着不良によ
る剥離が起こり易いという欠点があった。Furthermore, when forming a gel coat layer, predetermined lamination is performed after the gel coat layer is gelled, and the molding process is complicated. In particular, in the case of cast products, it is difficult to apply a gel coat layer in one molding process, and there are also disadvantages in that peeling is likely to occur due to poor adhesion to the base material.
本発明は従来の上記欠点に鑑みてこれを改良除去したも
のであって、アクリルプレポリマー等の樹脂材料の基材
に重合開始剤を0.01〜1.0wt%添加すると共に
、平均粒径が1.0μ蒙以下の炭酸カルシウム、水酸化
アルミニウム、珪酸塩化合物等の充填材を30〜70れ
%加え、更に必要に応じて架橋剤、離型剤1反応促進剤
、顔料等の添加物を加えて撹拌混合し、該混合物を脱気
してスラリー状組成物とし、該スラリー状組成物を成形
型に流し込んで加熱硬化させることにより耐摩耗性に優
れた人造大理石を得るようにしたことを特徴とする人造
大理石の製造方法を提供せんとするものである。In view of the above-mentioned drawbacks of the conventional technology, the present invention has been made to improve and eliminate the above drawbacks. 30 to 70% of fillers such as calcium carbonate, aluminum hydroxide, silicate compounds, etc. with a particle size of 1.0 μm or less are added, and if necessary, additives such as a crosslinking agent, a mold release agent, a reaction accelerator, and a pigment are added. is added and mixed with stirring, the mixture is deaerated to form a slurry composition, and the slurry composition is poured into a mold and heated to harden to obtain artificial marble with excellent wear resistance. The present invention aims to provide a method for producing artificial marble characterized by the following.
アクリルプレポリマー等の樹脂材料の基材は、50〜3
00cpの粘度を有することが望ましい。その理由は、
50cp以下であると、後述する微細な充填材が沈降し
てしまい、表面層の耐摩耗性を向上させることができな
いからである。また300cp以上であれば、多くの充
填材を入れることが困難であり、これまた表面層の耐摩
耗性を向上させることができないからである。材料は、
他にも不飽和ポリエステル等の使用が可能である。The base material of resin material such as acrylic prepolymer is 50 to 3
It is desirable to have a viscosity of 0.00 cp. The reason is,
This is because if it is less than 50 cp, fine fillers described below will settle, making it impossible to improve the wear resistance of the surface layer. Moreover, if it is 300 cp or more, it is difficult to add a large amount of filler, and the wear resistance of the surface layer cannot be improved. the material is,
Other materials such as unsaturated polyester can also be used.
重合開始剤としては、BPO等の有機過酸化物等のラジ
カル重合開始剤が適当である。該重合開始剤を0.01
〜1.Owt%の範囲にしたのは、0.01wt%以下
では重合しない場合があり、また重合したとしても時間
が多くかかるからである。1.0111t%以上では重
合の際の発熱で樹脂材料が発泡する虞があるためである
。As the polymerization initiator, radical polymerization initiators such as organic peroxides such as BPO are suitable. The polymerization initiator is 0.01
~1. The reason why the range of 0.01 wt% is set is that polymerization may not occur if the amount is less than 0.01 wt%, and even if it does polymerize, it will take a long time. This is because if the content exceeds 1.0111 t%, there is a risk that the resin material will foam due to heat generated during polymerization.
それに、炭酸カルシウム、水酸化アルミニウム。Also, calcium carbonate and aluminum hydroxide.
珪酸塩化合物(珪酸マグネシウム、珪酸カルシウム)等
の充填材の粒径を1.0μ鋼以下にした理由は、1.0
μm以上であれば、製品(人造大理石)表面に存在する
充填材の剥離が起こり易(、しかも耐摩耗性に欠けるた
めである。The reason why the particle size of fillers such as silicate compounds (magnesium silicate, calcium silicate) is set to 1.0μ steel or less is that
If it is .mu.m or more, the filler present on the surface of the product (artificial marble) is likely to peel off (and it lacks wear resistance).
また充填材の充填量を30〜7011t%の範囲に限定
した理由は、30wt%以下であれば樹脂材料の充分な
強度アップが得られず、70−t%以上であれば逆に充
填材の量が多くなり過ぎて成形性が悪くなり、却って物
性低下(曲げ、耐摩耗性)を来すためである。The reason why the filling amount of the filler was limited to the range of 30 to 7011 t% is that if it is less than 30 wt%, the strength of the resin material cannot be increased sufficiently, and if it is more than 70-t%, the filler This is because if the amount is too large, the moldability deteriorates, and the physical properties (bending and abrasion resistance) actually deteriorate.
製造の額序は、アクリルプレポリマー等の樹脂材料の基
材に重合開始剤を加え、これを溶解させた後に充填材を
加える。そして、必要に応じて架橋剤、離型剤9反応促
進剤、a料等の添加物を加えてミキサー等で混合し、更
に該混合物を真空脱気してスラリー状組成物を得る。次
に、該スラリー状組成物をガラス型、FRP型、金型等
の通常の注型に流し込み、加熱硬化させる。加熱条件は
、加熱温度を室温〜80℃の範囲とし、加熱時間を0゜
5〜30時間とする。The manufacturing process involves adding a polymerization initiator to a base material of a resin material such as an acrylic prepolymer, and then adding a filler after dissolving the polymerization initiator. Then, if necessary, additives such as a crosslinking agent, a release agent, a reaction accelerator, and a material are added and mixed using a mixer, and the mixture is further degassed under vacuum to obtain a slurry composition. Next, the slurry composition is poured into a conventional casting mold such as a glass mold, an FRP mold, or a metal mold, and is heated and cured. The heating conditions are such that the heating temperature ranges from room temperature to 80°C, and the heating time ranges from 0°C to 30 hours.
これにより、耐摩耗性に優れた人造大理石を得ることが
可能である。Thereby, it is possible to obtain artificial marble with excellent wear resistance.
尚、充填材の屈折率を樹脂の屈折率に近づけることによ
り透明感並びに高級質感のする製品を得ることが可能で
ある。また架橋剤、離型剤9反応促進剤、顔料等の添加
物は、製造時の緒特性及び製品の要求性能等に応じて適
宜量論えればよい。Note that by bringing the refractive index of the filler closer to that of the resin, it is possible to obtain a product with transparency and high-quality texture. Further, additives such as a crosslinking agent, a mold release agent, a reaction accelerator, and a pigment may be added in appropriate amounts depending on the initial characteristics during manufacturing, the required performance of the product, and the like.
次に示す表−1は、本発明に係る製造方法と従来の製造
方法とで人造大理石を製造し、耐摩耗性・透明感を比較
した結果を示すものである。耐摩耗性はテーパー摩耗試
験(JIS K6902 )の結果であり、単位はg/
100回である。透明感は試料厚を0.4鶴とした場合
の白色光の透過率を示すものである。Table 1 shown below shows the results of comparing the abrasion resistance and transparency of artificial marble produced by the production method according to the present invention and the conventional production method. Abrasion resistance is the result of a taper abrasion test (JIS K6902), and the unit is g/
100 times. Transparency indicates the transmittance of white light when the sample thickness is 0.4 mm.
(以下余白、次頁へ続く)
図面は表−1における試番1. 2. 7の充填材の平
均粒径と耐摩耗性との関係を示すものである。(Margins below, continued on next page) The drawings are trial number 1 in Table-1. 2. 7 shows the relationship between the average particle size and wear resistance of filler No. 7.
この図面及び表−1の結果から明らかなことは、充填材
の平均粒径はおよそ1.0μmで耐摩耗性の特性曲線が
急激に変化するということである。従って、充填材の平
均粒径は、1.0μm以下であればよい。好ましい充填
材の平均粒径は、表−1の賦香3乃至6に示す0.6μ
m以下の場合である。What is clear from this drawing and the results in Table 1 is that the wear resistance characteristic curve changes rapidly when the average particle size of the filler is approximately 1.0 μm. Therefore, the average particle size of the filler may be 1.0 μm or less. The average particle size of the preferable filler is 0.6μ as shown in Fragrances 3 to 6 in Table 1.
m or less.
平均粒径が0.6μm以下であると、耐摩耗性は非常に
優れた数値を示している。これは、充填材の粒径が微細
なためその比表面積が大きく、基材としての樹脂材料と
の密着力が増し、且つ充填密度が大であることににより
補強効果が充分に発揮されるからである。When the average particle size is 0.6 μm or less, the wear resistance shows very excellent values. This is because the particle size of the filler is small, so its specific surface area is large, which increases its adhesion to the resin material as a base material, and the high packing density provides a sufficient reinforcing effect. It is.
尚、本発明は上述の実施例に限定されるものではなく、
例えば充填材は他にも炭酸カルシウム。It should be noted that the present invention is not limited to the above-mentioned embodiments,
For example, another filler is calcium carbonate.
珪酸塩化合物、シリカ等の無機酸化物等が可能である。Silicate compounds, inorganic oxides such as silica, etc. are possible.
更に、基材としての樹脂材料は、不飽和ポリエステル等
が可能であると考えられる。Furthermore, it is considered that unsaturated polyester or the like can be used as the resin material as the base material.
以上説明したように本発明にあっては、アクリルプレポ
リマー等の樹脂材料に添加する充填材の平均粒径を1.
0μm以下としたので、充填材の比表面積が大きくなり
、該充填材と樹脂材料との密着力に優れたものが得られ
る。その結果、製品(人造大理石)表面の耐摩耗性にお
いても優れたものが得られるものである。As explained above, in the present invention, the average particle size of the filler added to the resin material such as acrylic prepolymer is set to 1.
Since it is set to 0 μm or less, the specific surface area of the filler becomes large, and an excellent adhesive force between the filler and the resin material can be obtained. As a result, the surface of the product (artificial marble) has excellent wear resistance.
図面は充填材の平均粒径と製品(人造大理石)の耐摩耗
性との関係を示すものである。The drawing shows the relationship between the average particle size of the filler and the wear resistance of the product (artificial marble).
Claims (1)
始剤を0.01〜1.0wt%添加すると共に、平均粒
径が1.0μm以下の炭酸カルシウム、水酸化アルミニ
ウム、珪酸塩化合物等の充填材を30〜70wt%加え
、更に必要に応じて架橋剤、離型剤、反応促進剤、顔料
等の添加物を加えて撹拌混合し、該混合物を脱気してス
ラリー状組成物とし、該スラリー状組成物を成形型に流
し込んで加熱硬化させることにより耐摩耗性に優れた人
造大理石を得るようにしたことを特徴とする人造大理石
の製造方法。1. Add 0.01 to 1.0 wt% of a polymerization initiator to the base material of a resin material such as acrylic prepolymer, and add calcium carbonate, aluminum hydroxide, silicate compounds, etc. with an average particle size of 1.0 μm or less. Add 30 to 70 wt% of filler, further add additives such as a crosslinking agent, a mold release agent, a reaction accelerator, and a pigment as necessary, stir and mix, and degas the mixture to obtain a slurry composition, A method for producing artificial marble, characterized in that artificial marble with excellent wear resistance is obtained by pouring the slurry composition into a mold and heating and curing it.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59158188A JPS6144747A (en) | 1984-07-27 | 1984-07-27 | Manufacture of artificial marble |
EP85305324A EP0171955B2 (en) | 1984-07-27 | 1985-07-25 | Simulated marble article |
DE8585305324T DE3576703D1 (en) | 1984-07-27 | 1985-07-25 | OBJECT FROM IMITATION OF MARBLE. |
US06/759,429 US4643921A (en) | 1984-07-27 | 1985-07-26 | Simulated marble article |
KR1019850005399A KR930001913B1 (en) | 1984-07-27 | 1985-07-27 | Simulated marble article |
CN85106057A CN85106057B (en) | 1984-07-27 | 1985-08-10 | Simulated marble article |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59158188A JPS6144747A (en) | 1984-07-27 | 1984-07-27 | Manufacture of artificial marble |
CN85106057A CN85106057B (en) | 1984-07-27 | 1985-08-10 | Simulated marble article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6144747A true JPS6144747A (en) | 1986-03-04 |
Family
ID=25741943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59158188A Pending JPS6144747A (en) | 1984-07-27 | 1984-07-27 | Manufacture of artificial marble |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS6144747A (en) |
CN (1) | CN85106057B (en) |
Cited By (6)
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JPH02275738A (en) * | 1989-04-17 | 1990-11-09 | Chihiro Kurokawa | Plastic molding material of natural stone pattern |
CN100374505C (en) * | 2005-09-23 | 2008-03-12 | 贾若华 | Natural texture irradiant artificial stone material and its production process |
JP2009212006A (en) * | 2008-03-05 | 2009-09-17 | Uchihashi Estec Co Ltd | Circuit breaking method for excessive current and protection element |
JP2009212007A (en) * | 2008-03-05 | 2009-09-17 | Uchihashi Estec Co Ltd | Protection element |
CN109305773A (en) * | 2018-10-26 | 2019-02-05 | 广东博瑞格新材料科技股份有限公司 | A kind of hilllock stone jade and preparation method thereof |
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US6287378B1 (en) * | 1996-09-03 | 2001-09-11 | Minerals Technologies, Inc. | Method of producing synthetic silicates and use thereof in glass production |
JP4857282B2 (en) * | 2004-12-17 | 2012-01-18 | チェイル インダストリーズ インコーポレイテッド | Foamed marble molded article and manufacturing method thereof |
CN103827411B (en) * | 2011-05-27 | 2016-09-28 | 美国赛尔尼特有限责任公司 | Artificial stone material and Related product thereof and method |
CN104479283B (en) * | 2014-12-15 | 2018-07-13 | 上海锦湖日丽塑料有限公司 | It is a kind of to exempt from spraying aesthetic resin composition and preparation method thereof with jade effect |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5381589A (en) * | 1976-12-27 | 1978-07-19 | Mitsubishi Rayon Co Ltd | Manufacturing of marble-like cured product |
JPS53115768A (en) * | 1977-03-22 | 1978-10-09 | Mitsubishi Rayon Co Ltd | Preparation of marblelike cured material |
JPS57155245A (en) * | 1981-03-23 | 1982-09-25 | Mitsubishi Rayon Co Ltd | Light-diffusing acrylic resin sheet |
JPS57162743A (en) * | 1981-03-30 | 1982-10-06 | Mitsubishi Rayon Co Ltd | Light-diffusing acrylic resin sheet |
JPS5891747A (en) * | 1978-11-22 | 1983-05-31 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | Use of ethylene copolymer composition |
JPS5986648A (en) * | 1982-10-05 | 1984-05-18 | デイナミ−ト・ノ−ベル・アクチエンゲゼルシヤフト | Injection mold resin comprising flowable settable acrylic acid ester, methacrylic acid ester and fine grain inorganic filler |
-
1984
- 1984-07-27 JP JP59158188A patent/JPS6144747A/en active Pending
-
1985
- 1985-08-10 CN CN85106057A patent/CN85106057B/en not_active Expired
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5381589A (en) * | 1976-12-27 | 1978-07-19 | Mitsubishi Rayon Co Ltd | Manufacturing of marble-like cured product |
JPS53115768A (en) * | 1977-03-22 | 1978-10-09 | Mitsubishi Rayon Co Ltd | Preparation of marblelike cured material |
JPS5891747A (en) * | 1978-11-22 | 1983-05-31 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | Use of ethylene copolymer composition |
JPS57155245A (en) * | 1981-03-23 | 1982-09-25 | Mitsubishi Rayon Co Ltd | Light-diffusing acrylic resin sheet |
JPS57162743A (en) * | 1981-03-30 | 1982-10-06 | Mitsubishi Rayon Co Ltd | Light-diffusing acrylic resin sheet |
JPS5986648A (en) * | 1982-10-05 | 1984-05-18 | デイナミ−ト・ノ−ベル・アクチエンゲゼルシヤフト | Injection mold resin comprising flowable settable acrylic acid ester, methacrylic acid ester and fine grain inorganic filler |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS638249A (en) * | 1986-06-27 | 1988-01-14 | フクビ化学工業株式会社 | Colored artificial stone formed article and manufacture |
JPH0517185B2 (en) * | 1986-06-27 | 1993-03-08 | Fukubi Kagaku Kogyo Kk | |
JPH02275738A (en) * | 1989-04-17 | 1990-11-09 | Chihiro Kurokawa | Plastic molding material of natural stone pattern |
CN100374505C (en) * | 2005-09-23 | 2008-03-12 | 贾若华 | Natural texture irradiant artificial stone material and its production process |
JP2009212006A (en) * | 2008-03-05 | 2009-09-17 | Uchihashi Estec Co Ltd | Circuit breaking method for excessive current and protection element |
JP2009212007A (en) * | 2008-03-05 | 2009-09-17 | Uchihashi Estec Co Ltd | Protection element |
CN109305773A (en) * | 2018-10-26 | 2019-02-05 | 广东博瑞格新材料科技股份有限公司 | A kind of hilllock stone jade and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN85106057A (en) | 1987-03-04 |
CN85106057B (en) | 1988-03-09 |
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