JPH0971486A - Production of calcium silicate compact - Google Patents
Production of calcium silicate compactInfo
- Publication number
- JPH0971486A JPH0971486A JP22637395A JP22637395A JPH0971486A JP H0971486 A JPH0971486 A JP H0971486A JP 22637395 A JP22637395 A JP 22637395A JP 22637395 A JP22637395 A JP 22637395A JP H0971486 A JPH0971486 A JP H0971486A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- calcium silicate
- slurry
- compact
- water
- 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.)
- Withdrawn
Links
- 239000000378 calcium silicate Substances 0.000 title claims abstract description 68
- 229910052918 calcium silicate Inorganic materials 0.000 title claims abstract description 68
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 title claims abstract description 68
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 19
- 229920005989 resin Polymers 0.000 claims abstract description 84
- 239000011347 resin Substances 0.000 claims abstract description 84
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000002002 slurry Substances 0.000 claims abstract description 35
- 238000002844 melting Methods 0.000 claims abstract description 22
- 230000008018 melting Effects 0.000 claims abstract description 22
- 238000002156 mixing Methods 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims description 17
- 238000000465 moulding Methods 0.000 claims description 15
- 239000000835 fiber Substances 0.000 claims description 7
- 238000001035 drying Methods 0.000 abstract description 12
- 239000004566 building material Substances 0.000 abstract description 3
- 238000004079 fireproofing Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 32
- 238000010521 absorption reaction Methods 0.000 description 20
- 239000002245 particle Substances 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 8
- 239000004816 latex Substances 0.000 description 8
- 229920000126 latex Polymers 0.000 description 8
- 230000018044 dehydration Effects 0.000 description 7
- 238000006297 dehydration reaction Methods 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000012783 reinforcing fiber Substances 0.000 description 6
- 239000003365 glass fiber Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 229920001187 thermosetting polymer Polymers 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000004580 weight loss Effects 0.000 description 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000920 calcium hydroxide Substances 0.000 description 3
- 235000011116 calcium hydroxide Nutrition 0.000 description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 3
- 239000000292 calcium oxide Substances 0.000 description 3
- 235000012255 calcium oxide Nutrition 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- UGGQKDBXXFIWJD-UHFFFAOYSA-N calcium;dihydroxy(oxo)silane;hydrate Chemical compound O.[Ca].O[Si](O)=O UGGQKDBXXFIWJD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000001027 hydrothermal synthesis Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- MKTRXTLKNXLULX-UHFFFAOYSA-P pentacalcium;dioxido(oxo)silane;hydron;tetrahydrate Chemical compound [H+].[H+].O.O.O.O.[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O MKTRXTLKNXLULX-UHFFFAOYSA-P 0.000 description 2
- 238000011085 pressure filtration Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910001653 ettringite Inorganic materials 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/18—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00939—Uses not provided for elsewhere in C04B2111/00 for the fabrication of moulds or cores
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/20—Resistance against chemical, physical or biological attack
- C04B2111/28—Fire resistance, i.e. materials resistant to accidental fires or high temperatures
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、珪酸カルシウム成
形体の製造方法に関する。さらに、詳しくは、軽量、高
強度、低吸水性、耐熱性、防火性等の特徴を有し、かつ
鋸引きや釘打ち等の加工性にも優れる、建築材料として
好適な珪酸カルシウム成形体の製造方法に関する。TECHNICAL FIELD The present invention relates to a method for producing a calcium silicate compact. More specifically, a calcium silicate compact suitable for a building material, which has characteristics such as light weight, high strength, low water absorption, heat resistance, and fire resistance, and is excellent in workability such as sawing and nailing. It relates to a manufacturing method.
【0002】[0002]
【従来の技術】従来、軽量、高耐熱性で鋸引きや釘打ち
等の加工性にも優れ、建築材料に使用される珪酸カルシ
ウム成形体として、珪酸カルシウム水和物、水分散性の
樹脂(例えば、カルボキシル基を含むスチレン−ブタジ
エン共重合体ラテックス)、カチオン型高分子凝集剤、
補強繊維および水を混合した水性スラリーを、加圧濾過
などの方法により脱水し、成形し、乾燥してなる合成木
材が提案されている(特公昭62−32148号公
報)。2. Description of the Related Art Conventionally, calcium silicate hydrate, a water-dispersible resin ( For example, a styrene-butadiene copolymer latex containing a carboxyl group), a cationic polymer flocculant,
A synthetic wood is proposed in which an aqueous slurry obtained by mixing reinforcing fibers and water is dehydrated by a method such as pressure filtration, molded, and dried (JP-B-62-32148).
【0003】しかし、この技術による成形体は、嵩密度
0.5g/cm3で曲げ強度が100kg/cm2前後と
天然木材に比較すると機械的強度は非常に低く、例えば
建築用の構造部材として使用することは困難であった。
また、非常に高い吸水性を示すために、耐凍害性に劣
る、表面が汚染され易い等の問題点を有しており塗装等
の大がかりな表面処理を施すことなしに屋外や水回りで
使用することも困難であった。However, the molded product obtained by this technique has a bulk density of 0.5 g / cm 3 and a bending strength of about 100 kg / cm 2, which is very low in mechanical strength as compared with natural wood. For example, it is used as a structural member for construction. It was difficult to use.
In addition, since it has extremely high water absorption, it has problems such as poor frost resistance and easy surface contamination, so it can be used outdoors or around water without extensive surface treatment such as painting. It was also difficult to do.
【0004】そこで、この成形体の問題点を改良する方
法として、珪酸カルシウム水和物−樹脂−補強繊維等か
らなる成形体に、(1)カップリング剤を添加する方法
(特公平5−17187号公報、特開昭63−1000
49号公報)、(2)セメント用分散剤を添加する方法
(特開昭62−123053号公報)(3)水と反応し
てエトリンガイトを生成する物質を添加する方法(特開
平3−3635号公報)、(4)アルカリ金属またはマ
グネシウムの硫酸塩を添加する方法(特開平6ー488
07号公報)、(5)樹脂に熱硬化性水溶性カチオン樹
脂と高分子ラテックスとを組み合わせて用いる方法(特
開平1−119554号公報)、(6)樹脂に特定の合
成樹脂ラテックス、エマルジョンを用いる方法(特公平
4ー72788号公報、特開昭64ー72950号公
報)、(7)撥水剤を添加する方法(特開平1−264
948号公報)、(8)樹脂に粉末状樹脂を用いる方法
(特開平4−6137号公報)、等が提案されている。Therefore, as a method for improving the problems of this molded article, (1) a method of adding a coupling agent to a molded article composed of calcium silicate hydrate-resin-reinforcing fiber (Japanese Patent Publication No. 5-17187). JP-A-63-1000
49), (2) a method of adding a dispersant for cement (JP-A-62-123053), (3) a method of adding a substance which reacts with water to form ettringite (JP-A-3-3635). Gazette), (4) Method of adding sulfate of alkali metal or magnesium (JP-A-6-488)
No. 07), (5) a method of using a thermosetting water-soluble cationic resin and a polymer latex in combination with the resin (JP-A-1-119554), and (6) a resin containing a specific synthetic resin latex or emulsion. Method used (Japanese Patent Publication No. 4-72788, Japanese Patent Application Laid-Open No. 64-72950), (7) Method of adding water repellent (Japanese Patent Application Laid-Open No. 1-264)
948), (8) a method of using a powdered resin as the resin (Japanese Patent Application Laid-Open No. 4-6137), and the like.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、上記
(1)〜(6)に記載の方法による成形体は、機械的強
度に向上は認められるものの、吸水性についてはまだ高
いレベルにある。また、(7)に記載の方法による成形
体は、低吸水性にはなっているものの機械的強度がほと
んど向上していないことに加え、ポリジメチルシリオキ
サン等の高価な撥水剤を使用するため、成形体の製造コ
ストの大幅なアップにつながり実用的なものではなかっ
た。However, although the molded articles produced by the methods described in the above (1) to (6) are found to have improved mechanical strength, their water absorption is still at a high level. In addition, the molded product according to the method described in (7) has low water absorption, but has little improvement in mechanical strength, and uses an expensive water repellent such as polydimethylsilyloxane. Therefore, the production cost of the molded body is significantly increased, and it is not practical.
【0006】さらに、これらの方法はいずれも樹脂をラ
テックスやエマルジョンとして添加するため、成形時に
スラリーの脱水性が悪くなったり、脱水の際に水と共に
樹脂が抜け出てしまったりすることがあるために、その
対策が必要になる。また、ラテックスやエマルジョンタ
イプの樹脂には通常界面活性剤等がかなり含有されてい
るため、成形時に脱水により生じた水を排水するのに特
殊な処理が必要になったりもし、これらは製造コストア
ップの原因になる。Further, in all of these methods, since the resin is added as a latex or emulsion, the dehydration property of the slurry may be deteriorated at the time of molding, or the resin may escape with water during the dehydration. , That measure is needed. In addition, since latex and emulsion type resins usually contain a considerable amount of surfactants, special treatment may be required to drain the water generated by dehydration during molding, which increases manufacturing costs. Cause
【0007】この様なラテックスやエマルジョンタイプ
の樹脂を添加することに起因して発生する問題点を解決
する方法としては、(8)に記載の方法が提案されてお
り、(8)に記載の方法によれば、成形体の加工性や加
工時の発塵性も改良される。しかしながら、(8)に記
載の方法には成形体の強度向上、低吸水化に関しては、
何等記載がない。The method described in (8) has been proposed as a method for solving the problems caused by the addition of such latex or emulsion type resin, and described in (8). According to the method, the processability of the molded product and the dust generation property during the process are also improved. However, in the method described in (8), the strength of the molded body is improved and the water absorption is reduced.
There is no description.
【0008】本発明の目的は、高強度、低吸水性であっ
て、軽量、耐熱性、防火性等の特徴を有し、加工性にも
優れる珪酸カルシウム成形体をより低コストで製造でき
る方法を提供することにある。The object of the present invention is a method of producing a calcium silicate compact having high strength, low water absorption, light weight, heat resistance, fire resistance, etc. and excellent workability at a lower cost. To provide.
【0009】[0009]
【課題を解決するための手段】本発明者らは、上記の様
な状況を鑑み、鋭意研究を重ねた結果、樹脂を繊維状に
してスラリー中に添加しかつスラリーを成形した後にそ
の樹脂の溶融温度以上に加熱保持し、樹脂を溶融、流動
させることによって、ラテックスやエマルジョンタイプ
の樹脂を添加することに起因して発生する前述の問題点
を解決できることに加え、高強度、低吸水性の珪酸カル
シウム成形体が得られることを見い出し、本発明を完成
するに至った。Means for Solving the Problems The inventors of the present invention have conducted extensive studies in view of the above-mentioned circumstances, and as a result, the resin was made into a fibrous form and added to the slurry, and after the slurry was formed, the resin By heating and maintaining the temperature above the melting temperature to melt and flow the resin, in addition to being able to solve the above-mentioned problems that occur due to the addition of a latex or emulsion type resin, high strength and low water absorption It has been found that a calcium silicate compact can be obtained, and the present invention has been completed.
【0010】すなわち、本発明は、珪酸カルシウム水和
物、樹脂および水を混合したスラリーを脱水成形し、乾
燥して珪酸カルシウム成形体を製造する方法において、
上記樹脂として繊維状樹脂を用い、かつ成形した後に繊
維状樹脂の溶融温度以上に加熱保持することを特徴とす
る珪酸カルシウム成形体の製造方法、である。以下、本
発明を詳しく説明する。That is, the present invention relates to a method for producing a calcium silicate compact by dehydrating and molding a slurry obtained by mixing calcium silicate hydrate, a resin and water, and drying the slurry.
A method for producing a calcium silicate compact, which comprises using a fibrous resin as the resin and, after molding, holding the fibrous resin at a temperature higher than the melting temperature of the fibrous resin. Hereinafter, the present invention will be described in detail.
【0011】本発明に係る珪酸カルシウム水和物とは、
生石灰、消石灰等の石灰質原料と珪石粉等の珪酸質原料
とをそれぞれ水中に分散させて水性スラリーとした後、
水熱反応させて得られるものをいい、トバモライト、ゾ
ノトライト等の結晶質のものやCSH−I、CSH−I
Iと呼ばれる比較的結晶性の低いものを例示できる。石
灰質原料と珪酸質原料との配合割合は、合成する珪酸カ
ルシウム水和物の種類によって異なり特に限定されるも
のではないが、トバモライトの場合はCaO/SiO2
モル比で0.8程度、ゾノトライトの場合には1程度と
するのが好ましい。The calcium silicate hydrate according to the present invention is
After calcining raw materials such as quick lime and slaked lime and siliceous raw materials such as silica stone powder are dispersed in water to form an aqueous slurry,
A substance obtained by a hydrothermal reaction is a crystalline substance such as tobermorite or xonotlite, or CSH-I or CSH-I.
One having a relatively low crystallinity called I can be exemplified. The blending ratio of the calcareous raw material and the siliceous raw material varies depending on the type of calcium silicate hydrate to be synthesized and is not particularly limited, but in the case of tobermorite, CaO / SiO 2
The molar ratio is preferably about 0.8, and in the case of xonotlite, it is preferably about 1.
【0012】珪酸カルシウム水和物は、水性スラリーと
して得られるが、本発明においてはこのスラリーをその
まま乾燥せずに用いてもよいし、スラリーを乾燥して粉
末にしたものを用いてもよい。本発明の製造方法は、樹
脂として繊維状樹脂を用いることを特徴とするが、樹脂
は熱可塑性樹脂、熱硬化性樹脂の何れであってもよい。The calcium silicate hydrate is obtained as an aqueous slurry, but in the present invention, this slurry may be used as it is without being dried, or the slurry may be dried and made into powder. The production method of the present invention is characterized in that a fibrous resin is used as the resin, but the resin may be either a thermoplastic resin or a thermosetting resin.
【0013】熱可塑性樹脂としては、ポリアミド、ポリ
エステル、ポリビニルアルコール、ポリエチレン、ポリ
プロピレン、アラミド、アクリル等を例示できるが、こ
れらに限定されるものではない。また、熱硬化性樹脂と
しては、エポキシ、フェノール、メラミン等を例示でき
るが、これらに限定されるものではない。Examples of the thermoplastic resin include polyamide, polyester, polyvinyl alcohol, polyethylene, polypropylene, aramid, and acryl, but are not limited thereto. Examples of the thermosetting resin include epoxy, phenol, melamine, etc., but are not limited to these.
【0014】樹脂は単独で用いても二種類以上を混合し
て用いてもよい。本発明に用いる繊維状樹脂は、径が5
0μm以下で長さが1〜50mmの範囲のものを用いる
ことが好ましく、径が20μm以下で長さが3〜20m
mの範囲のものであればさらに好ましい。径が太すぎた
り、長さが短か過ぎたりすると高強度の成形体が得るの
が難しくなる。一方、長さが長過ぎるとスラリー中で均
一に分散させることが難しく成形体の諸物性低下の原因
になる。The resins may be used alone or in combination of two or more. The fibrous resin used in the present invention has a diameter of 5
It is preferable to use one having a length of 0 μm or less and a length of 1 to 50 mm, and a diameter of 20 μm or less and a length of 3 to 20 m.
More preferably, it is in the range of m. If the diameter is too large or the length is too short, it becomes difficult to obtain a high-strength molded product. On the other hand, if the length is too long, it is difficult to uniformly disperse it in the slurry, which causes deterioration of various physical properties of the molded product.
【0015】本発明に用いる繊維状樹脂は、添加量につ
いて特に制限はなく、どのような物性の成形体を製造す
るかにより適宜選択すればよいが、珪酸カルシウム水和
物100重量部に対して3〜30重量部とすることが好
ましい。添加量が少ないと珪酸カルシウム成形体の高強
度化、低吸水化が難しく、多すぎると耐熱性、防火性が
低下する。The amount of the fibrous resin used in the present invention is not particularly limited, and may be appropriately selected depending on the physical properties of the molded product to be produced, but with respect to 100 parts by weight of calcium silicate hydrate. It is preferably 3 to 30 parts by weight. If the amount of addition is small, it is difficult to increase the strength and water absorption of the calcium silicate compact, and if it is too large, the heat resistance and fire resistance deteriorate.
【0016】本発明の製造方法は、樹脂として、繊維状
樹脂に加えて、粉末状の樹脂を添加してもよい。また、
本発明の効果のうち、珪酸カルシウム成形体の高強度化
のみ、あるいは高強度化と低吸水性化のみを達成したい
のであれば、水溶性樹脂、エマルジョンタイプの樹脂を
繊維状樹脂と併用することも可能である。本発明の製造
方法は、必要に応じ補強繊維を添加してもよい。補強繊
維の添加は高強度化に有効である。In the production method of the present invention, a powdered resin may be added as the resin in addition to the fibrous resin. Also,
Among the effects of the present invention, if it is desired to achieve only high strength of the calcium silicate compact, or only high strength and low water absorption, use a water-soluble resin or an emulsion type resin in combination with the fibrous resin. Is also possible. In the production method of the present invention, reinforcing fibers may be added if necessary. Addition of reinforcing fibers is effective in increasing strength.
【0017】本発明に用いる補強繊維は、ガラス繊維、
カーボン繊維、ロックウール、パルプ、レーヨン等であ
り、これらは単独で用いても二種類以上を混合して用い
てもよい。なお、有機繊維を用いる場合には、樹脂と有
機繊維との合計量を珪酸カルシウム水和物100重量部
に対して30重量部以下にすることが好ましい。30重
量部を越えた場合には、耐熱性、防火性の低下が見られ
るようになる。The reinforcing fibers used in the present invention are glass fibers,
Carbon fiber, rock wool, pulp, rayon, etc. may be used alone or in combination of two or more kinds. When using organic fibers, the total amount of resin and organic fibers is preferably 30 parts by weight or less with respect to 100 parts by weight of calcium silicate hydrate. When it exceeds 30 parts by weight, the heat resistance and fire resistance are deteriorated.
【0018】本発明の製造方法では、珪酸カルシウム水
和物の一部を、ワラストナイト、セピオライト、タル
ク、水酸化アルミニウム等、一般に充填材として知られ
ている無機物に置換することも可能であるが、置換率は
20%以下にすることが好ましい。20%を越えると珪
酸カルシウム成形体の強度が低下する傾向が見られる。
本発明の製造方法は、まず、珪酸カルシウム水和物、繊
維状樹脂および水、さらに必要に応じて添加する補強繊
維等を混合して均一な水性スラリーとする。原料の投入
順序や混合方法については、各原料が均一に混合されれ
ば特に限定されるものではなく、状況に応じて決定すれ
ばよい。またスラリー中には、各原料の均一混合を促進
するための分散剤、成形時のスラリーの濾水性、脱水性
を向上するための凝集剤、成形性、保形性を向上するた
めの成形助剤等を必要に応じて添加してもよい。In the production method of the present invention, it is also possible to replace a part of the calcium silicate hydrate with an inorganic substance generally known as a filler such as wollastonite, sepiolite, talc and aluminum hydroxide. However, the substitution rate is preferably 20% or less. If it exceeds 20%, the strength of the calcium silicate compact tends to decrease.
In the production method of the present invention, first, a calcium silicate hydrate, a fibrous resin, water, and reinforcing fibers added as necessary are mixed to form a uniform aqueous slurry. The order of feeding the raw materials and the mixing method are not particularly limited as long as the raw materials are uniformly mixed, and may be determined according to the situation. In the slurry, a dispersant for promoting uniform mixing of each raw material, a coagulant for improving drainage and dehydration of the slurry at the time of molding, a molding aid for improving moldability and shape retention. You may add agents etc. as needed.
【0019】この様にして得られたスラリーを加圧濾過
などの方法によって脱水し、加圧成形して成形体とす
る。成形方法としては、プレス成形法、抄造成形法、押
し出し成形法等の従来公知の方法が目的、用途に応じて
適宜採用できる。本発明の製造方法は、スラリーを脱水
し成形した後、スラリーを乾燥して水分を除去すること
に加えて繊維状樹脂の溶融温度以上に加熱し、保持する
ことを特徴とする。加熱し、保持する方法としては、電
気乾燥器による方法、電磁波照射による方法が例示でき
る。The slurry thus obtained is dehydrated by a method such as pressure filtration and pressure-molded to obtain a molded body. As a molding method, a conventionally known method such as a press molding method, a papermaking molding method and an extrusion molding method can be appropriately adopted depending on the purpose and application. The manufacturing method of the present invention is characterized in that after the slurry is dehydrated and molded, the slurry is dried to remove water, and in addition, the slurry is heated to or above the melting temperature of the fibrous resin and held. Examples of the method of heating and holding include a method using an electric dryer and a method using electromagnetic wave irradiation.
【0020】繊維状樹脂を溶融させ、流動させることに
よって、珪酸カルシウム成形体の高強度化が可能にな
る。繊維状樹脂の溶融温度以上に保持する時間は、温
度、成形体の形状、樹脂の種類等の条件により決定する
ことが好ましい。また、まず、乾燥が終了して水分を含
まない状態の成形体を得て、ついで水分を含まない状態
で成形体を繊維状樹脂の溶融温度以上に加熱保持して繊
維状樹脂の溶融流動させれば、さらなる高強度化に加え
て低吸水化も可能となる。By melting and flowing the fibrous resin, it becomes possible to increase the strength of the calcium silicate compact. The time for which the fibrous resin is held at the melting temperature or higher is preferably determined by conditions such as temperature, shape of the molded product, and type of resin. Further, first, a molded body in a state of containing no moisture after drying is obtained, and then the molded body is heated and held at a temperature not lower than the melting temperature of the fibrous resin to melt and flow the fibrous resin in a state of containing no moisture. If this is the case, in addition to higher strength, lower water absorption becomes possible.
【0021】この場合、水分を除去するための乾燥は、
繊維状樹脂が溶融する条件で行われても、溶融しない条
件で行われてもよく、加熱乾燥、電磁波照射による乾
燥、真空乾燥等の方法が例示できる。繊維状樹脂の溶融
温度以上に加熱保持し溶融させ、流動させる処理の回数
は、スラリーの構成および目的とする物性によって、2
度以上でもよい。In this case, the drying for removing water is
It may be performed under the condition that the fibrous resin is melted or not melted, and examples thereof include methods such as heat drying, drying by electromagnetic wave irradiation, and vacuum drying. The number of times that the fibrous resin is heated and held at a temperature equal to or higher than the melting temperature to melt and flow the resin depends on the composition of the slurry and the desired physical properties.
It may be more than once.
【0022】本発明でいう樹脂の溶融温度とは、JIS
K 6910に準じて測定した融点をいう。なお、こ
の溶融温度が幅をもって測定される場合には、その上限
温度をいう。熱硬化性樹脂に対しては、架橋反応を進行
させていない段階の樹脂について測定した融点をいう。
また、本発明で乾燥が終了するとは、乾燥のための処理
による重量減少が見られない状態をいい、例えば、繊維
状ポリプロピレン樹脂を用いた場合に190℃で5時間
加熱乾燥し、加熱による重量減少が見られなくなった状
態をいう。The melting temperature of the resin referred to in the present invention is defined by JIS
Melting point measured according to K 6910. When the melting temperature is measured with a range, it means the upper limit temperature. For thermosetting resins, the melting point measured for the resin at the stage where the crosslinking reaction has not proceeded.
In addition, the term “drying completed” in the present invention means a state in which no weight loss is observed due to the treatment for drying. For example, when a fibrous polypropylene resin is used, it is dried by heating at 190 ° C. for 5 hours, The state where the decrease is no longer seen.
【0023】本発明の珪酸カルシウム成形体の製造方法
は、得られた珪酸カルシウム成形体を高強度化すること
ができるが、以下の様な機構により達成されるものと考
えられる。まず、ラテックスやエマルジョンタイプの樹
脂を添加した場合は、珪酸カルシウム水和物粒子内部に
も樹脂が入り込んでしまうため、珪酸カルシウム水和物
粒子同士の接着に有効に作用する樹脂の量が実際に添加
した量よりも少なくなる。これに対し繊維状等の固体状
樹脂を添加した場合には、樹脂は溶融しても珪酸カルシ
ウム水和物粒子内部まで容易に入り込めるレベルまで粘
度が低下しないため、珪酸カルシウム水和物粒子同士の
接着に有効に作用する樹脂の量が多くなる。The method for producing a calcium silicate compact according to the present invention can enhance the strength of the obtained calcium silicate compact, but it is considered to be achieved by the following mechanism. First, when a latex or emulsion type resin is added, the resin also enters inside the calcium silicate hydrate particles, so the amount of resin that effectively acts on the adhesion between calcium silicate hydrate particles is actually Less than the amount added. On the other hand, when a fibrous solid resin is added, the viscosity of the resin does not decrease to such a level that it can easily enter the inside of the calcium silicate hydrate particles even if it is melted. The amount of resin that effectively acts on adhesion increases.
【0024】さらに、同じ固体状樹脂であっても、粉末
状樹脂の場合は珪酸カルシウム水和物粒子間に介在して
元々隣接している水和物粒子間の補強に寄与するが、繊
維状樹脂の場合には粒子間にまたがる様に介在して隣接
していない水和物粒子間をも橋かけ的に補強するため
に、より有効な補強効果を発揮できる。次に、スラリー
を形成し、脱水し、成形してから、乾燥により水分を除
去した珪酸カルシウム成形体の状態で、さらに、繊維状
樹脂の溶融温度以上に加熱し、保持して樹脂を溶融する
処理により、珪酸カルシウム成形体のさらなる高強度化
に加え、低吸水化も可能となる。Further, even if the same solid resin is used, in the case of powdery resin, it is interposed between the calcium silicate hydrate particles and contributes to the reinforcement between the hydrate particles that are originally adjacent to each other. In the case of a resin, since it intervenes so as to straddle the particles and also bridges the hydrate particles that are not adjacent to each other in a bridging manner, a more effective reinforcing effect can be exhibited. Next, a slurry is formed, dehydrated, molded, and then dried in a state of a calcium silicate compact from which water is removed, and further heated to a temperature above the melting temperature of the fibrous resin and held to melt the resin. By the treatment, not only the strength of the calcium silicate compact can be further increased, but also the water absorption can be reduced.
【0025】従来、低吸水性の珪酸カルシウム成形体
は、撥水剤等の高価な添加剤を添加することにより得ら
れていたが、本発明によれば撥水剤等を添加することな
く低吸水性の珪酸カルシウム成形体が得られる。従来技
術による成形体(例えば特公昭62−32148号公報
による成形体)等は、電子顕微鏡観察(SEM観察)に
よれば樹脂は珪酸カルシウム水和物の粒子間に介在して
いるものの三次元の連続性には乏しく、そのために強度
不足に加え高い吸水性をも示すものと考えられる。Conventionally, a calcium silicate compact having a low water absorption has been obtained by adding an expensive additive such as a water repellent. However, according to the present invention, the low water absorbency is not added. A water-absorbing calcium silicate compact is obtained. According to an electron microscope observation (SEM observation), the molded body according to the prior art (for example, the molded body according to Japanese Patent Publication No. 62-32148) is three-dimensional though the resin is present between the particles of the calcium silicate hydrate. The continuity is poor, and therefore it is considered that it exhibits high water absorption in addition to insufficient strength.
【0026】しかし、スラリーを成形し、乾燥が終了し
た後に繊維状樹脂の溶融温度以上に加熱保持して繊維状
樹脂を溶融させ、流動させることで、三次元方向に連続
性が高い樹脂の構造が形成され、珪酸カルシウム成形体
の強度がさらに向上すると共に低吸水性になるものと考
えられる。なお、珪酸カルシウム成形体を乾燥する条件
は、繊維状樹脂が溶融する条件であつても溶融しない条
件であつてもよいが、溶融する条件で乾燥を行った場合
でも、乾燥終了後に繊維状樹脂の溶融温度以上に加熱保
持することが低吸水性の珪酸カルシウム成形体を得る上
で好ましい。乾燥し水分を除去した後に、樹脂の溶融温
度以上に加熱し、保持することで、水の蒸発時に樹脂層
に生じた構造上の変化が三次元方向に連続性のあるもの
となり低吸水性の珪酸カルシウム成形体が得られるもの
と考えられる。However, after the slurry is formed and dried, the fibrous resin is melted by being heated and maintained at a temperature not lower than the melting temperature of the fibrous resin, and the resin is made to flow. Is considered to be formed, the strength of the calcium silicate compact is further improved, and the water absorbency becomes low. The condition for drying the calcium silicate compact may be a condition in which the fibrous resin melts or a condition in which the fibrous resin does not melt. It is preferable to heat and maintain the temperature above the melting temperature in order to obtain a calcium silicate compact having low water absorption. After drying and removing water, by heating and holding above the melting temperature of the resin, the structural changes that occur in the resin layer during water evaporation become continuous in the three-dimensional direction, resulting in low water absorption. It is considered that a calcium silicate compact can be obtained.
【0027】熱硬化性樹脂を用いた場合は、樹脂の溶融
温度以上に加熱保持した後、さらに加熱して樹脂の架橋
反応を進行させて樹脂を硬化させる。なお、本発明にお
いては、成形後の一連の加熱処理は樹脂を劣化させない
条件で行うことが望ましい。When a thermosetting resin is used, the resin is heated and held at a temperature not lower than the melting temperature of the resin and then further heated to accelerate the crosslinking reaction of the resin to cure the resin. In the present invention, it is desirable that the series of heat treatments after molding be performed under conditions that do not deteriorate the resin.
【0028】[0028]
【発明の実施の形態】以下、実施例によりさらに本発明
を具体的に説明する。なお、実施例における物性等は以
下に示す方法で測定した。 (1) 曲げ強度 JIS A 1408に準じて測定した。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in more detail below with reference to Examples. The physical properties and the like in the examples were measured by the methods described below. (1) Bending strength It was measured according to JIS A 1408.
【0029】(2) 吸水量 200×200×20mmの試験体を温度20℃、相対
湿度60%の室内に含水率が平衡に達するまで放置した
後、重量測定しこれを乾燥重量Md(g)とする。次に
この試験体を200×200mmの面を水平にして20
〜25℃の水中に上面が水面下約30mmの位置になる
ように置き、24時間放置する。24時間経過した後、
試験体を取り出し表面に付着している水を湿布でふき取
り、直ちに重量測定しこれを吸水時の重量Mw(g)と
する。吸水量は次式によって算出した。(2) Water absorption amount A test piece of 200 × 200 × 20 mm was allowed to stand in a room at a temperature of 20 ° C. and a relative humidity of 60% until the water content reached equilibrium, and then weighed to obtain a dry weight M d (g ). Next, this test body is placed on a surface of 200 × 200 mm in a horizontal position of 20
Place in water at -25 ° C so that the upper surface is about 30 mm below the surface of the water, and leave it for 24 hours. After 24 hours,
The test body is taken out, water adhering to the surface is wiped off with a compress, and the weight is immediately measured, and this is taken as the weight M w (g) when absorbing water. The water absorption amount was calculated by the following formula.
【0030】 吸水量(g/cm3 )=(Mw−Md )/V V:乾燥重量測定時の試験体について行った外寸測定結
果より算出した試験体体積(cm3 )Water absorption amount (g / cm 3 ) = (M w −M d ) / V V: test body volume (cm 3 ) calculated from the outer size measurement result performed on the test body during dry weight measurement
【0031】[0031]
【実施例1】珪石粉と消石灰とをCaO/SiO2モル
比が1になるように混合し、珪石粉と消石灰との合計重
量に対して10倍量の水を加えてオートクレーブ中で撹
拌しながら温度210℃、圧力19kg/cm2で6時
間、水熱反応させて珪酸カルシウム水和物スラリーを得
た。Example 1 Silica stone powder and slaked lime were mixed so that a CaO / SiO 2 molar ratio was 1, water was added in an amount 10 times the total weight of silica stone powder and slaked lime, and the mixture was stirred in an autoclave. While performing hydrothermal reaction at a temperature of 210 ° C. and a pressure of 19 kg / cm 2 for 6 hours, a calcium silicate hydrate slurry was obtained.
【0032】このスラリーに珪酸カルシウム水和物10
0重量部に対して繊維状ポリプロピレン樹脂(径:12
μm、長さ:5mm、溶融温度:174℃)を15重量
部、ガラス繊維3重量部を添加し、均一になるように混
合した。このスラリーを300×300mmの型枠に注
入して、加圧脱水して成形し、水分が蒸発してしまい重
量減少が見られなくなるまで190℃で5時間加熱乾燥
して珪酸カルシウム成形体を得た。珪酸カルシウム成形
体の試験結果を表1に示した。Calcium silicate hydrate 10 was added to this slurry.
Fibrous polypropylene resin (diameter: 12
μm, length: 5 mm, melting temperature: 174 ° C.), 15 parts by weight, and 3 parts by weight of glass fiber were added and mixed so as to be uniform. This slurry is poured into a mold of 300 × 300 mm, dehydrated under pressure to be molded, and dried by heating at 190 ° C. for 5 hours until moisture disappears and weight reduction is not obtained to obtain a calcium silicate compact. It was The test results of the calcium silicate compact are shown in Table 1.
【0033】[0033]
【実施例2】実施例1と同様の珪酸カルシウム水和物ス
ラリーに珪酸カルシウム水和物100重量部に対して繊
維状ポリエステル樹脂(繊維径:10μm、繊維長10
mm,溶融温度:260℃)10重量部、ガラス繊維6
重量部を添加し、均一になるように混合した。Example 2 The same calcium silicate hydrate slurry as in Example 1 was added to 100 parts by weight of calcium silicate hydrate and a fibrous polyester resin (fiber diameter: 10 μm, fiber length 10).
mm, melting temperature: 260 ° C.) 10 parts by weight, glass fiber 6
Parts by weight were added and mixed to be uniform.
【0034】このスラリーを300×300mmの型枠
に注入して、加圧脱水成形後、270℃で重量減少が見
られなくなるまで4時間加熱乾燥して、珪酸カルシウム
成形体を得た。 珪酸カルシウム成形体の試験結果を表
1に示した。This slurry was poured into a mold of 300 × 300 mm, subjected to pressure dehydration molding, and then heat-dried at 270 ° C. for 4 hours until no weight reduction was observed to obtain a calcium silicate compact. The test results of the calcium silicate compact are shown in Table 1.
【0035】[0035]
【実施例3】実施例1と同様のスラリーを300×30
0mmの型枠に注入して、加圧脱水して、成形し、13
0℃で8時間加熱乾燥し加熱による重量減少が見られな
くなることを確認した後、190℃で3時間加熱して珪
酸カルシウム成形体を得た。珪酸カルシウム成形体の試
験結果を表1に示した。Example 3 The same slurry as in Example 1 was used at 300 × 30.
It is poured into a 0 mm form, dehydrated under pressure, molded, and
After heating and drying at 0 ° C. for 8 hours and confirming that no weight loss due to heating was observed, heating at 190 ° C. for 3 hours gave a calcium silicate compact. The test results of the calcium silicate compact are shown in Table 1.
【0036】[0036]
【実施例4】実施例2と同様のスラリーを300×30
0mmの型枠に注入して、加圧脱水して、成形し、15
0℃で7時間加熱乾燥し加熱による重量減少が見られな
くなることを確認した後、270℃で2時間加熱して、
珪酸カルシウム成形体を得た。 珪酸カルシウム成形体
の試験結果を表1に示した。Example 4 The same slurry as in Example 2 was added to 300 × 30.
Pour into a 0 mm form, dewatering under pressure, molding, 15
After heating and drying at 0 ° C for 7 hours and confirming that weight loss due to heating is not seen, heating at 270 ° C for 2 hours,
A calcium silicate compact was obtained. The test results of the calcium silicate compact are shown in Table 1.
【0037】[0037]
【実施例5】実施例1と同様の珪酸カルシウム水和物ス
ラリーに珪酸カルシウム水和物100重量部に対して繊
維状ポリエチレン樹脂(繊維径:20μm、繊維長:1
0mm,溶融温度:166℃)20重量部、ガラス繊維
3重量部を添加し、均一になるように混合した。Example 5 A calcium silicate hydrate slurry similar to that of Example 1 was added to 100 parts by weight of calcium silicate hydrate to form a fibrous polyethylene resin (fiber diameter: 20 μm, fiber length: 1).
0 mm, melting temperature: 166 ° C.) 20 parts by weight, glass fibers 3 parts by weight were added and mixed so as to be uniform.
【0038】このスラリーを300×300mmの型枠
に注入して、加圧脱水して、成形し、120℃で10時
間加熱乾燥し加熱による重量減少が見られなくなること
を確認した後、180℃で2時間加熱して、珪酸カルシ
ウム成形体を得た。珪酸カルシウム成形体の試験結果を
表1に示した。This slurry was poured into a 300 × 300 mm mold, dehydrated under pressure, molded, and dried by heating at 120 ° C. for 10 hours. After confirming that no weight loss due to heating was observed, 180 ° C. By heating for 2 hours, a calcium silicate compact was obtained. The test results of the calcium silicate compact are shown in Table 1.
【0039】[0039]
【比較例1】実施例1と同様の珪酸カルシウム水和物ス
ラリーに、珪酸カルシウム水和物100重量部に対して
アクリル酸エステル共重合体エマルジョン(成膜した際
の溶融温度:139℃)10重量部(固形分換算)、ガ
ラス繊維3重量部を添加し、均一になるように混合し
た。[Comparative Example 1] Acrylic ester copolymer emulsion (melting temperature during film formation: 139 ° C) was added to 100 parts by weight of calcium silicate hydrate in the same calcium silicate hydrate slurry as in Example 1. Parts by weight (in terms of solid content) and 3 parts by weight of glass fiber were added and mixed to be uniform.
【0040】このスラリーを300×300mmの型枠
に注入して、加圧脱水成形し、120℃で10時間加熱
乾燥して、珪酸カルシウム成形体を得た。 成形体の試
験結果を表1に示した。This slurry was poured into a mold of 300 × 300 mm, subjected to pressure dehydration molding, and heated and dried at 120 ° C. for 10 hours to obtain a calcium silicate compact. The test results of the molded product are shown in Table 1.
【0041】[0041]
【比較例2】ポリプロピレン樹脂を粉末状(平均粒径:
60μm)としたこと以外は実施例1と同様の方法で珪
酸カルシウム成形体を得た。 成形体の試験結果を表1
に示した。Comparative Example 2 Polypropylene resin powder (average particle size:
A calcium silicate compact was obtained in the same manner as in Example 1 except that the thickness was 60 μm). Table 1 shows the test results of the molded products.
It was shown to.
【0042】[0042]
【比較例3】加圧脱水後、130℃で12時間の加熱の
みを行った以外は、実施例1と同様の方法で珪酸カルシ
ウム成形体を得た。 成形体の試験結果を表1に示し
た。Comparative Example 3 A calcium silicate compact was obtained in the same manner as in Example 1 except that only heating at 130 ° C. for 12 hours was performed after pressure dehydration. The test results of the molded product are shown in Table 1.
【0043】[0043]
【表1】 [Table 1]
【0044】[0044]
【発明の効果】本発明の珪酸カルシウム成形体の製造方
法は、従来の珪酸カルシウム系合成木材の特徴に加え
て、高強度、低吸水性をも具備した珪酸カルシウム成形
体を製造することができる。すなわち、軽量、耐熱性、
防火性等の特徴を有し、さらに、従来のものに比べて極
めて高強度で、しかも吸水性が低い、加工性にも優れる
建築材料として好適な珪酸カルシウム成形体を、より低
コストで製造することが可能である。The method for producing a calcium silicate compact of the present invention can produce a calcium silicate compact having high strength and low water absorption in addition to the characteristics of the conventional calcium silicate-based synthetic wood. . That is, light weight, heat resistance,
A calcium silicate compact, which has characteristics such as fire resistance and is extremely high in strength as compared with conventional ones, has low water absorption, and is excellent in workability as a building material, is manufactured at a lower cost. It is possible.
Claims (1)
混合したスラリーを脱水成形し、乾燥して珪酸カルシウ
ム成形体を製造する方法において、上記樹脂として繊維
状樹脂を用い、かつ成形した後に繊維状樹脂の溶融温度
以上に加熱保持することを特徴とする珪酸カルシウム成
形体の製造方法。1. A method for producing a calcium silicate compact by dehydrating and molding a slurry obtained by mixing calcium silicate hydrate, a resin and water, and using a fibrous resin as the resin, and after molding the fiber. A method for producing a calcium silicate compact, which comprises heating and holding the resin at a temperature equal to or higher than the melting temperature of the resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22637395A JPH0971486A (en) | 1995-09-04 | 1995-09-04 | Production of calcium silicate compact |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22637395A JPH0971486A (en) | 1995-09-04 | 1995-09-04 | Production of calcium silicate compact |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0971486A true JPH0971486A (en) | 1997-03-18 |
Family
ID=16844120
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22637395A Withdrawn JPH0971486A (en) | 1995-09-04 | 1995-09-04 | Production of calcium silicate compact |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0971486A (en) |
-
1995
- 1995-09-04 JP JP22637395A patent/JPH0971486A/en not_active Withdrawn
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| Date | Code | Title | Description |
|---|---|---|---|
| A300 | Withdrawal of application because of no request for examination |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 20021105 |