JPH053421B2 - - Google Patents
Info
- Publication number
- JPH053421B2 JPH053421B2 JP31462486A JP31462486A JPH053421B2 JP H053421 B2 JPH053421 B2 JP H053421B2 JP 31462486 A JP31462486 A JP 31462486A JP 31462486 A JP31462486 A JP 31462486A JP H053421 B2 JPH053421 B2 JP H053421B2
- Authority
- JP
- Japan
- Prior art keywords
- magnesia
- whiskers
- materials
- magnesia whiskers
- matrix
- 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.)
- Expired - Lifetime
Links
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 76
- 239000000395 magnesium oxide Substances 0.000 claims description 38
- 239000000463 material Substances 0.000 claims description 19
- 239000011159 matrix material Substances 0.000 claims description 16
- 229910010272 inorganic material Inorganic materials 0.000 claims description 14
- 239000011147 inorganic material Substances 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 7
- 238000001027 hydrothermal synthesis Methods 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 2
- 239000012784 inorganic fiber Substances 0.000 claims description 2
- 239000003562 lightweight material Substances 0.000 claims description 2
- 239000003513 alkali Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 9
- 238000011049 filling Methods 0.000 description 8
- 239000003365 glass fiber Substances 0.000 description 8
- 239000013078 crystal Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000010425 asbestos Substances 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 229910052895 riebeckite Inorganic materials 0.000 description 5
- 239000011398 Portland cement Substances 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 239000000378 calcium silicate Substances 0.000 description 4
- 229910052918 calcium silicate Inorganic materials 0.000 description 4
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 4
- 230000003014 reinforcing effect Effects 0.000 description 4
- 239000012783 reinforcing fiber Substances 0.000 description 4
- 230000002194 synthesizing effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004566 building material Substances 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012763 reinforcing filler Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012777 electrically insulating material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Landscapes
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
[産業上の利用分野]
本発明はマグネシアウイスカーで補強された無
機質材料に係り、詳しくは建築用内外装材料、船
舶等の内装材、保温材料など曲げ強度、耐衝撃性
等を要求される材料として極めて有用なマグネシ
アウイスカーで補強された無機質材料に関するも
のである。
[従来の技術]
従来、建築物の内外装用材料、船舶の内装材、
保温材料のマトリツクスとしては、普通ポルトラ
ンドセメントや焼石こう、石灰質と珪酸質との水
熱合成によつて生成する珪酸カルシウム等の無機
質材料が使用されている。また、このような無機
質材料の曲げ強度、耐衝撃性等の特性の改善のた
めに、強化繊維が複合されている。
強化繊維の代表的なものとしては、石綿があ
る。石綿はポルトランドセメントとの馴染みが良
く、石綿スレート板等として各種建築材料、保温
材料に広く使用されている。しかしながら、石綿
は人体に対して有害で、発癌性の物質であるとの
見解が特に欧州、米国で取り上げられ、今後使用
禁止措置が取られようとしている現状にある。
このようなことから、石綿の代替繊維として、
耐アルカリ性ガラス繊維、カーボン繊維、その他
化学繊維等が実用化されつつある。
[発明が解決しようとする問題点]
これらの強化繊維のうち、耐アルカリ性ガラス
繊維は一般的なEガラス組成に耐アルカリ性を付
与させるために、酸化ジルコニウムを10数%添加
混合し繊維化したものであるが、耐アルカリ性と
いえどもその特性にも限度があり、例えば、マト
リツクスが普通ポルトランドセメントである場
合、耐アルカリ性ガラス繊維は数年で補強繊維と
しての効果が期待出来なくなる。また、マトリツ
クスが水熱合成して得られる珪酸カルシウム硬化
体である場合には、マトリツクスと耐アルカリ性
繊維を混合成形後、高温高圧養生を行なうと、急
激なアルカリの析出と高温高圧の水蒸気のために
耐アルカリ性ガラス繊維は完全に劣化し、補強硬
化を全く示さなくなる。
カーボン繊維はガラス繊維のような問題点はな
く、従来よりプラスチツクの補強材として利用さ
れているが、高価なために建築材料のような低コ
ストを要求される材料には不適当である。
また、各種化学繊維は耐熱性等の面において十
分な特性が得られず、やはり建築材料等には不適
当である。
[問題点を解決するための手段]
本発明者らは上記従来の問題点を解決する各種
無機質材料の改質方法、強化方法について研究を
行なうと共に、安価な無機質充填材料の開発研究
を行なつた結果、無機質材料の強化充填材料とし
て極めて優れた効果を奏するマグネシアウイスカ
ーの合成に成功するに至つた。そして、本発明者
らは、このマグネシアウイスカーを水硬性物質や
水熱合成されてできる珪酸カルシウム水和物等の
無機硬化体の充填材料として適用すべく更に研究
を重ね、本発明を完成させた。
本発明は、新規な合成マグネシアウイスカーを
無機質材料に充填、複合化することにつて、樹脂
の耐曲げ強度、耐衝撃強度等の力学的性質等の特
性を改善するものであつて、水硬性物質や水熱合
成されてできるマトリツクスと、合成された針状
のマグネシアウイスカーとを含むことを特徴とす
る。
以下、本発明につきさらに詳細に説明する。
まず、本発明における充填材料としてのマグネ
シアウイスカーについて詳しく説明する。
マグネシアは従来から耐火物材料、電気絶縁材
料として利用されてきているが、電融マグネシア
といえども、水和性があることが最大の欠点であ
ることが指摘されている。本発明者らは、この水
和性の改善について、鋭意研究を行つた結果、単
結晶のマグネシアウイスカーの合成に成功した。
そして、本発明者らは熱可塑性樹脂への強化充
填材料としてのマグネシアウイスカーの合成条件
を種々検討した結果、第1図(顕微鏡写真(×
500))に示すようなマグネシアウイスカーを大量
に合成することに成功した。
第1図のような単結晶マグネシアウイスカー
は、ハロゲン化物とマグネシウム塩類との混合物
の溶融塩を水蒸気雰囲気で650〜900℃に加熱する
ことによつて比較的低温かつ短時間で容易に析出
させることができる。析出するマグネシアウイス
カーの繊維長、繊維径は上記加熱条件等によつて
異なるが、一般には、繊維長30μm〜6mm、繊維
径1〜5μmで、アスペクト比が30〜3000前後の
ものが得られる。
このようなマグネシアウイスカーを水硬性物質
や水熱合成されてできる珪酸カルシウム水和物等
のマトリツクスの強化充填材料として使用する場
合には、ウイスカー形状が、マトリツクスへの充
填方法や成形方法、例えば、ロール混練法、押出
成形法、モールド成形法、射出成形法、抄造法等
によつて制約される場合があるため、充填方法や
成形方法に適合した形状のマグネシアウイスカー
を得るべく、合成条件を適宜選択する必要があ
る。
マグネシアウイスカーは、マトリツクスへの分
散性又は加工性等の向上のために、ステアリン酸
等の脂肪酸又はその塩類、あるいはシランカツプ
リング剤等で表面処理することも有効である。特
に、シランカツプリング剤で処理することにより
力学的にも優れた効果を得ることができる。
本発明においては、このようなマグネシアウイ
スカーをマトリツクス100重量部に対して2〜30
重量部充填するのが好ましい。マグネシアウイス
カーの含有量がマトリツクス100重量部に対して
2重量部未満であると、本発明による十分な改善
効果が得られ難く、逆に、マグネシアウイスカー
の含有量がマトリツクス100重量部に対して30重
量部を超えるとマトリツクスの成形性等が低下す
る場合がある。
ところで、本発明のマグネシアウイスカーで補
強された無機質材料は、常法に従つて、マトリツ
クス材料に所定量のマグネシアウイスカーを充填
混練して、押出成形、モールド成形、抄造法等に
より成形することにより、容易に得られるが、成
形性の改善やその他軽量化等を目的として、各種
の補助材料を充填使用することも好ましい態様で
ある。補助材料としては、パルプ、無機質繊維、
化学繊維、軽量材、その他各種充填材料が挙げら
れ、これらの1種又は2種以上を用いることがで
きる。
「作用」
ウイスカーは、細い繊維状結晶で、ひげ結晶と
もいわれる。ウイスカーの特徴は、細いほど結晶
の欠陥(転位など)が非常に少ないことで、螺旋
転位の存在ではよじれが起きたり、弾性限界が低
かつたりすることで結晶の完全性が検出できる。
従つて、マグネシアウイスカーは大きな強度をも
つことになり、複合材料における繊維強化材とし
て有用である。
本発明において、マグネシアウイスカーが特に
無機質材料の強化用充填材料として優れた効果を
奏する理由は、針状の形態を有し、かつアスペク
ト比が大きいことにあり、その形態上の特性から
優れた補強効果を有する上に、マトリツクスとの
馴染みも良好である。しかも、マグネシアウイス
カーは耐水性、耐アルカリ性、耐熱性等にも優れ
るので、複合材料のこれらの特性の改善効果も極
めて大きい。
[実施例]
以下、実施例を挙げて本発明を更に具体的に説
明するが、本発明はその要旨を超えない限り、以
下の実施例に限定されるものではない。
実施例 1
消石灰、珪操土をその調合割合がCaO/SiOモ
ル比で0.85となるように調整混合し、この調合原
料乾物100重量部に対して、各々、マグネシアウ
イスカーを3、7、11、13、15重量部、更にパル
プ3重量部加えて混合し、次いで水を加えてスラ
リー状として、モールド成形法により生板を成形
した。成形された生板を、183℃の条件で8時間
オートクレーブ養生し、自然冷却後、80℃で24時
間乾燥して試験片を得た。得られた試験片につい
て諸特性を調べ、その結果を第1表に締した。
[Industrial Application Field] The present invention relates to an inorganic material reinforced with magnesia whiskers, and more specifically to materials that require bending strength, impact resistance, etc., such as interior and exterior materials for buildings, interior materials for ships, and heat insulation materials. This invention relates to an inorganic material reinforced with magnesia whiskers, which is extremely useful as a magnet. [Conventional technology] Conventionally, interior and exterior materials for buildings, interior materials for ships,
Inorganic materials such as Portland cement, calcined gypsum, and calcium silicate produced by hydrothermal synthesis of calcareous and silicic acid materials are commonly used as the matrix of heat-retaining materials. Further, in order to improve the properties such as bending strength and impact resistance of such inorganic materials, reinforcing fibers are composited. Asbestos is a typical reinforcing fiber. Asbestos is compatible with Portland cement and is widely used in various building materials and heat-insulating materials, such as asbestos slate boards. However, the view that asbestos is harmful to the human body and carcinogenic has been raised particularly in Europe and the United States, and there are plans to ban its use in the future. For this reason, as an alternative fiber to asbestos,
Alkali-resistant glass fibers, carbon fibers, and other chemical fibers are being put into practical use. [Problems to be solved by the invention] Among these reinforcing fibers, alkali-resistant glass fibers are made by adding and mixing 10% zirconium oxide to give alkali resistance to the general E glass composition. However, even though it is alkali resistant, there is a limit to its properties; for example, if the matrix is ordinary Portland cement, the alkali resistant glass fiber will no longer be expected to be effective as a reinforcing fiber after a few years. In addition, when the matrix is a hardened calcium silicate obtained by hydrothermal synthesis, if the matrix and alkali-resistant fibers are mixed and molded and then cured at high temperature and high pressure, rapid alkali precipitation and high temperature and high pressure steam may occur. The alkali-resistant glass fibers deteriorate completely and show no reinforcing hardening. Carbon fiber does not have the same problems as glass fiber and has been used as a reinforcing material for plastics, but its high price makes it unsuitable for materials that require low cost, such as building materials. In addition, various chemical fibers do not have sufficient properties in terms of heat resistance and the like, and are therefore unsuitable for use as building materials. [Means for Solving the Problems] The present inventors have conducted research on methods for modifying and strengthening various inorganic materials to solve the above-mentioned conventional problems, and have also conducted research and development on inexpensive inorganic filler materials. As a result, we succeeded in synthesizing magnesia whiskers, which are extremely effective as reinforcing fillers for inorganic materials. The present inventors have further conducted research to apply this magnesia whisker as a filling material for hydraulic substances and inorganic hardened bodies such as hydrothermally synthesized calcium silicate hydrate, and have completed the present invention. . The present invention improves the mechanical properties such as bending strength and impact strength of the resin by filling and compounding the novel synthetic magnesia whiskers into an inorganic material. It is characterized by containing a matrix formed by hydrothermal synthesis of carbon dioxide and synthesized acicular magnesia whiskers. The present invention will be explained in more detail below. First, magnesia whiskers as a filling material in the present invention will be explained in detail. Magnesia has been used as a refractory material and an electrically insulating material, but it has been pointed out that the biggest drawback of fused magnesia is that it is hydrated. The present inventors conducted intensive research on improving this hydration property, and as a result, succeeded in synthesizing single-crystal magnesia whiskers. The present inventors investigated various conditions for synthesizing magnesia whiskers as a reinforcing filler material for thermoplastic resins.
We succeeded in synthesizing a large amount of magnesia whiskers as shown in 500)). Single-crystal magnesia whiskers as shown in Figure 1 can be easily precipitated at a relatively low temperature and in a short time by heating a molten salt of a mixture of halides and magnesium salts to 650 to 900°C in a steam atmosphere. I can do it. The fiber length and fiber diameter of the precipitated magnesia whiskers vary depending on the heating conditions, etc., but generally, the fiber length is 30 μm to 6 mm, the fiber diameter is 1 to 5 μm, and the aspect ratio is about 30 to 3000. When such magnesia whiskers are used as a reinforcing filling material for a matrix such as a hydraulic substance or hydrothermally synthesized calcium silicate hydrate, the shape of the whiskers depends on the method of filling the matrix and the method of molding, e.g. Since there may be restrictions due to the roll kneading method, extrusion molding method, mold molding method, injection molding method, paper making method, etc., the synthesis conditions must be adjusted appropriately to obtain magnesia whiskers with a shape that is suitable for the filling method and molding method. You need to choose. It is also effective to surface-treat magnesia whiskers with a fatty acid such as stearic acid or a salt thereof, or a silane coupling agent, etc., in order to improve dispersibility in a matrix or processability. In particular, excellent mechanical effects can be obtained by treatment with a silane coupling agent. In the present invention, such magnesia whiskers are used in an amount of 2 to 30 parts by weight per 100 parts by weight of the matrix.
It is preferable to fill parts by weight. When the content of magnesia whiskers is less than 2 parts by weight per 100 parts by weight of the matrix, it is difficult to obtain a sufficient improvement effect according to the present invention; If the amount exceeds 1 part by weight, the moldability of the matrix may deteriorate. By the way, the inorganic material reinforced with magnesia whiskers of the present invention can be obtained by filling and kneading a predetermined amount of magnesia whiskers into a matrix material in accordance with a conventional method, and then forming it by extrusion molding, molding, paper forming, etc. Although easily obtained, it is also a preferable embodiment to fill with various auxiliary materials for the purpose of improving moldability and reducing weight. Auxiliary materials include pulp, inorganic fibers,
Chemical fibers, lightweight materials, and other various filler materials can be mentioned, and one or more of these can be used. ``Operation'' Whiskers are thin fibrous crystals and are also called whisker crystals. A characteristic of whiskers is that the thinner they are, the fewer crystal defects (such as dislocations) there are, and in the presence of screw dislocations, the integrity of the crystal can be detected by the occurrence of kinks and a low elastic limit.
Therefore, magnesia whiskers have high strength and are useful as fiber reinforcing materials in composite materials. In the present invention, the reason why magnesia whiskers are particularly effective as a reinforcing filler material for inorganic materials is that they have an acicular shape and a large aspect ratio. In addition to being effective, it also has good compatibility with the matrix. Moreover, since magnesia whiskers are also excellent in water resistance, alkali resistance, heat resistance, etc., the effect of improving these properties of the composite material is extremely large. [Examples] Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to the following Examples unless it exceeds the gist thereof. Example 1 Slaked lime and siliceous earth were adjusted and mixed so that the molar ratio of CaO/SiO was 0.85, and 3, 7, 11, and 10% of magnesia whisker were added to 100 parts by weight of the dry matter of the mixed raw materials, respectively. 13 and 15 parts by weight and an additional 3 parts by weight of pulp were added and mixed, and then water was added to form a slurry, which was then molded into a green board using a molding method. The molded green board was cured in an autoclave at 183°C for 8 hours, cooled naturally, and then dried at 80°C for 24 hours to obtain a test piece. Various properties of the obtained test pieces were investigated, and the results are summarized in Table 1.
【表】
第1表より、耐アルカリ性ガラス繊維では補強
効果が乏しいのに対し、本発明に係るマグネシア
ウイスカーでは著しく高い補強効果が得られるこ
とが明らかである。
実施例 2
普通ポルトランドセメント94重量部にマグネシ
アウイスカー又は耐アルカリ性ガラス繊維を6重
量部加えて混合し、セメント水比40%で混練し成
形した。得られた成形体の3日材令における自然
養生、オートクレーブ養生(183℃、8時間)に
ついくの物性を測定し、その結果を第2表に示し
た。[Table] From Table 1, it is clear that the alkali-resistant glass fibers have a poor reinforcing effect, whereas the magnesia whiskers according to the present invention have a significantly high reinforcing effect. Example 2 6 parts by weight of magnesia whiskers or alkali-resistant glass fibers were added to 94 parts by weight of ordinary Portland cement, mixed, kneaded at a cement water ratio of 40%, and molded. The physical properties of the obtained molded product after natural curing and autoclave curing (183° C., 8 hours) after 3 days of age were measured, and the results are shown in Table 2.
【表】
第2表より、耐アルカリ性ガラス繊維では、オ
ートクレーブ養生を行なうことにより、強度が大
幅に低下してしまうのに対し、本発明に係るマグ
ネシアウイスカーでは、オートクレーブ養生を行
なつても極めて良好な結果が得られることが明ら
かである。
[発明の効果]
以上詳述した通り、本発明の無機質材料はマト
リツクスに合成針状マグネシアウイスカーを充填
してなるものであつて、マグネシアウイスカーの
優れた改善効果により、耐曲げ強度、耐衝撃強度
等の機械的特性が著しく向上されると共に、耐水
性、耐アルカリ性、耐熱性についても優れた改善
効果が得られる。
また、オートクレーブ処理してもマグネシアウ
イスカーは全く劣化しないので、複合材料の製造
プロセスにオートクレーブ養生を組み込むことが
可能であり、短い製造時間にて高強度材を製造す
ることが可能とされる。[Table] From Table 2, the strength of alkali-resistant glass fibers is significantly reduced by autoclave curing, whereas the magnesia whisker according to the present invention has excellent strength even after autoclave curing. It is clear that good results can be obtained. [Effects of the Invention] As detailed above, the inorganic material of the present invention is formed by filling a matrix with synthetic acicular magnesia whiskers, and due to the excellent improving effects of the magnesia whiskers, the inorganic material has improved bending resistance and impact resistance. The mechanical properties such as these are significantly improved, and excellent improvement effects are also obtained in water resistance, alkali resistance, and heat resistance. Furthermore, since magnesia whiskers do not deteriorate at all even after autoclave treatment, autoclave curing can be incorporated into the composite material manufacturing process, making it possible to manufacture high-strength materials in a short manufacturing time.
第1図はマグネシアウイスカーの繊維形状を示
す顕微鏡写真である。
FIG. 1 is a micrograph showing the fiber shape of magnesia whiskers.
Claims (1)
リツクスと、合成された針状のマグネシアウイス
カーとを含むことを特徴とするマグネシアウイス
カーで補強された無機質材料。 2 補助材料としてパルプ、無機質繊維、化学繊
維、軽量材及び充填材よりなる群から選ばれる1
種又は2種以上を含むことを特徴とする特許請求
の範囲第1項に記載のマグネシアウイスカーで補
強された無機質材料。 3 マグネシアウイスカーの含有量がマトリツク
ス100重量部に対して2〜30重量部であることを
特徴とする特許請求の範囲第1項又は第2項に記
載のマグネシアウイスカーで補強された無機質材
料。[Scope of Claims] 1. An inorganic material reinforced with magnesia whiskers, characterized by containing a matrix obtained by a hydraulic substance or hydrothermal synthesis, and synthesized acicular magnesia whiskers. 2 Auxiliary materials selected from the group consisting of pulp, inorganic fibers, chemical fibers, lightweight materials, and fillers 1
The inorganic material reinforced with magnesia whiskers according to claim 1, characterized in that it contains one or more kinds of magnesia whiskers. 3. The inorganic material reinforced with magnesia whiskers according to claim 1 or 2, wherein the content of magnesia whiskers is 2 to 30 parts by weight based on 100 parts by weight of the matrix.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31462486A JPS63162560A (en) | 1986-12-25 | 1986-12-25 | Magnesia whisker reinforced inorganic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31462486A JPS63162560A (en) | 1986-12-25 | 1986-12-25 | Magnesia whisker reinforced inorganic material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63162560A JPS63162560A (en) | 1988-07-06 |
| JPH053421B2 true JPH053421B2 (en) | 1993-01-14 |
Family
ID=18055548
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP31462486A Granted JPS63162560A (en) | 1986-12-25 | 1986-12-25 | Magnesia whisker reinforced inorganic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63162560A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT393677B (en) * | 1990-03-22 | 1991-11-25 | Veitscher Magnesitwerke Ag | METHOD FOR PRODUCING FIBROUS MAGNESIUM OXIDE |
| JP4572527B2 (en) * | 2003-10-24 | 2010-11-04 | パナソニック電工株式会社 | Method for manufacturing ceramic building materials |
-
1986
- 1986-12-25 JP JP31462486A patent/JPS63162560A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63162560A (en) | 1988-07-06 |
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