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JPS5842151B2 - hardened body - Google Patents
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JPS5842151B2 - hardened body - Google Patents

hardened body

Info

Publication number
JPS5842151B2
JPS5842151B2 JP6230278A JP6230278A JPS5842151B2 JP S5842151 B2 JPS5842151 B2 JP S5842151B2 JP 6230278 A JP6230278 A JP 6230278A JP 6230278 A JP6230278 A JP 6230278A JP S5842151 B2 JPS5842151 B2 JP S5842151B2
Authority
JP
Japan
Prior art keywords
ceracola
spherical
cured
lightweight
impregnating
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
Application number
JP6230278A
Other languages
Japanese (ja)
Other versions
JPS54154423A (en
Inventor
均 安村
正彦 白石
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.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan 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 Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Priority to JP6230278A priority Critical patent/JPS5842151B2/en
Publication of JPS54154423A publication Critical patent/JPS54154423A/en
Publication of JPS5842151B2 publication Critical patent/JPS5842151B2/en
Expired legal-status Critical Current

Links

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  • Aftertreatments Of Artificial And Natural Stones (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Description

【発明の詳細な説明】 本発明はセラコラ硬化体に関し、詳しくは直径0.01
〜10闘、かさ密度0.02〜0.811/−の軽量球
状セラコラを主材とする原料から得られる成形体に含浸
性物質を含浸、硬化してなるセラコラ硬化体に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cured body of Ceracola, and more specifically, a cured body having a diameter of 0.01
The present invention relates to a cured body of Ceracola obtained by impregnating and curing a molded body obtained from a raw material mainly composed of lightweight spherical Ceracola having a bulk density of 0.02 to 0.811/- with an impregnating substance.

従来、軽量のセラコラ硬化体としては、軽量骨材を混入
したもの2発泡剤を用いて硬化体中に気泡を混入したも
の、針状セラコラを用いて多量の水を混合したもの等が
知られている。
Conventionally, lightweight cured Ceracola materials include those mixed with lightweight aggregate, those with air bubbles mixed into the cured material using a foaming agent, and those made with needle-shaped Ceracola mixed with a large amount of water. ing.

しかし、これらのセラコラ硬化体は強度的に不十分であ
り、また経済性に劣るなどの欠点があった。
However, these cured Ceracola products have drawbacks such as insufficient strength and poor economic efficiency.

この欠点を改良したものとして、本発明者らは新規な軽
量球状セラコラを原料としたセラコラ成形体を開発した
In order to improve this drawback, the present inventors have developed a Ceracola molded article using a new lightweight spherical Ceracola as a raw material.

しかしながら、このセラコラ硬化体も耐水性2表面性等
において必ずしも十分とは云えない。
However, this cured product of Ceracola is not necessarily sufficient in terms of water resistance, surface properties, etc.

本発明は、このような欠点を解消し、あわせて強度を向
上せしめたセラコラ硬化体を提供することを目的として
いる。
The object of the present invention is to eliminate such drawbacks and provide a cured Ceracola product with improved strength.

本発明に使用する軽量球状セラコラの製造方法の1例を
述べれば、半水セラコラ、二水セッコウなどを原料とし
て酸性溶媒中で100〜180°Gの温度で加熱攪拌し
て水熱反応させることによって得られる。
One example of the method for manufacturing the lightweight spherical Ceracola used in the present invention is to heat and stir in an acidic solvent at a temperature of 100 to 180°G to cause a hydrothermal reaction using semihydrous Ceracola, dihydrate gypsum, etc. as raw materials. obtained by.

このようにして得られる球状セラコラは実質的に繊維状
のα型半水セツコウのからみ合いにより形成されたもの
であり、顕微鏡的観察によるとイガグリ状ないしマリモ
状を呈している。
The spherical ceracola thus obtained is substantially formed by the intertwining of fibrous α-type hemihydrate snails, and microscopically shows a burr-like or marimo-like shape.

本発明においては、水熱反応終了後の球状のα型半水セ
ツコウスラリーをそのまS素材として用いてもよく、あ
るいは固液分離したのちの湿った状態の球状α型半水セ
ツコウ、これをさらに乾燥した球状α型半水セツコウや
これを焼成して得られる球状の可溶性もしくは不溶性無
水セラコラを用いることもできる。
In the present invention, the spherical α-type hemihydrate slurry after the completion of the hydrothermal reaction may be used as the S material, or the wet spherical α-type hemihydrate slurry after solid-liquid separation may be used as the S material. It is also possible to use spherical α-type hemihydrous ceracolla obtained by further drying or spherical soluble or insoluble anhydrous ceracola obtained by firing this.

こSで乾燥処理はたとえば50〜80℃の温度で1〜8
時間行なえばよく、焼成は乾燥セラコラを200〜10
00℃で1〜3時間行なえばよい。
For example, the drying process is performed at a temperature of 50 to 80°C for 1 to 8 hours.
All you need to do is to do it for a certain amount of time.
What is necessary is just to carry out at 00 degreeC for 1 to 3 hours.

なお、球状セラコラは、その製造条件によって異なるけ
れども、通常は直径0.01〜10mm、かさ密度0.
02〜o、s g/c111である。
Spherical Ceracola usually has a diameter of 0.01 to 10 mm and a bulk density of 0.05 mm, although it varies depending on the manufacturing conditions.
02~o, s g/c111.

上記の軽量球状セラコラから成形体を作るに際しては軽
量球状セラコラを単独で用いてもよく、あるいは繊維状
セツコウ、アスベスト等の補強剤やパーライト、シラス
バルーンなどの充てん剤を適宜配合してもよい。
When making a molded object from the above-mentioned lightweight spherical Ceracola, the lightweight spherical Ceracola may be used alone, or a reinforcing agent such as fibrous slag, asbestos, or a filler such as pearlite or shirasu balloon may be appropriately blended.

また成形に際しては原料セラコラに対し三水セラコラに
変換するに必要な理論水和量以上の水を加えて水和硬化
させる方法。
In addition, during molding, water is added to the raw material Ceracola in an amount greater than the theoretical hydration amount required to convert it to trihydric Ceracola, resulting in hydration and curing.

水和硬化の際に硬化促進剤および/または結合剤を添加
して行なう方法、結合剤のみを加えて硬化させる方法な
ど任意の手段を採ることができ、次いで圧縮、押出し、
流し込み、抄造、吹付は等の成形法により成形して軽量
のセラコラ成形体を得る。
Any method can be used, such as adding a curing accelerator and/or binder during hydration curing, or adding only a binder and curing, followed by compression, extrusion,
A lightweight Ceracola molded body is obtained by molding by a molding method such as pouring, paper forming, or spraying.

こへで結合剤としては水性結合剤と無水性結合剤のいず
れも使用可能であり、結合剤の例としては、ポリビニル
アルコール、カルボキシメチルセルロース、ヒドロオキ
シエチルセルロース、ポリアクリルアミド、ポリアクリ
ル酸、ポリエチレンオキシドなどの水溶性有機重合体、
酢酸ビニルエマルジョン、アクリル樹脂エマルジョンな
どの水分散性有機重合体、水ガラス、けい酸ソーダなど
の水溶性無機化合物、アルミナゾル、シリカゾルなどの
水分散系コロイド形成性無機化合物、セメント、石こう
などの水硬性化合物およびこれらの混合物等がある。
Both aqueous and anhydrous binders can be used as binders; examples of binders include polyvinyl alcohol, carboxymethyl cellulose, hydroxyethyl cellulose, polyacrylamide, polyacrylic acid, polyethylene oxide, etc. water-soluble organic polymer,
Water-dispersible organic polymers such as vinyl acetate emulsions and acrylic resin emulsions, water-soluble inorganic compounds such as water glass and sodium silicate, water-dispersible colloid-forming inorganic compounds such as alumina sol and silica sol, and hydraulic properties such as cement and gypsum. These include compounds and mixtures thereof.

これら結合剤は球状セラコラの重量に基いて0.01〜
100倍の範囲で添加すればよい。
These binders range from 0.01 to 0.01 based on the weight of the spherical Ceracola.
It may be added in a range of 100 times.

また硬化促進剤としては硫酸マグネシウム、塩化カルシ
ウム、硫酸カリウム、硝酸カリウム、硫酸鋼などを適宜
使用することができる。
Further, as a hardening accelerator, magnesium sulfate, calcium chloride, potassium sulfate, potassium nitrate, steel sulfate, etc. can be used as appropriate.

成形体を乾燥処理して自由水を除去した後、含浸性物質
を含浸させる。
After drying the molded body to remove free water, it is impregnated with an impregnating substance.

こ〜で含浸性物質としては、たとえばメタクリル酸メチ
ル、スチレンなどの重合性単量体、液状ゴム、ポリウレ
タンなどの重合性プレポリマー、熱硬化性樹脂、熱可塑
性樹脂、ワックス、アスファルト、イオウ、金属などが
あり、最終製品たるセラコラ硬化体の使用目的等を考慮
して適宜選択すればよい。
Examples of impregnating substances include methyl methacrylate, polymerizable monomers such as styrene, liquid rubber, polymerizable prepolymers such as polyurethane, thermosetting resins, thermoplastic resins, wax, asphalt, sulfur, and metals. etc., and may be appropriately selected in consideration of the purpose of use of the cured Ceracola product as the final product.

また含浸性物質の種類によっては使用時に溶剤等に溶解
したり加熱して溶融する等の処理をして用いることが必
要である。
Furthermore, depending on the type of impregnating substance, it may be necessary to perform a treatment such as dissolving it in a solvent or heating it to melt it before use.

含浸処理は任意の手段によって行なうことができ、たと
えば含浸性物質に成形体を浸漬する方法、スプレーや刷
毛塗りなどによって部分的(表面的)に含浸させる方法
などを適宜採用でき、含浸性物質の粘性等の性質や使用
目的を考慮して決定すればよい。
The impregnation treatment can be carried out by any method, such as immersing the molded body in the impregnating substance or partially (superficially) impregnating it by spraying or brushing. It may be determined in consideration of properties such as viscosity and purpose of use.

さらに含浸処理を行なうに際しては、減圧下、常圧下お
よび加圧下のいずれの状態としてもよい。
Further, when performing the impregnation treatment, it may be carried out under reduced pressure, normal pressure, or increased pressure.

本発明に用いる軽量セラコラ成形体は細孔が多数あって
空隙率が高いので、適当な手段を選定することにより含
浸性物質を所望の程度に含浸させることが可能である。
Since the lightweight Ceracola molded article used in the present invention has a large number of pores and a high porosity, it is possible to impregnate it with the impregnating substance to a desired degree by selecting an appropriate means.

なお、含浸処理において、必要に応じて硬化剤等の補助
成分を添加しうろことは勿論である。
Incidentally, in the impregnation treatment, it goes without saying that auxiliary components such as a curing agent may be added as necessary.

含浸処理後、硬化させて得られるセラコラ硬化体は軽量
で高強度であるという特性のほかに、耐水性や表面硬度
等についても改善されたものである。
After the impregnation treatment, the cured Ceracola product obtained by curing is lightweight and has high strength, as well as improved water resistance and surface hardness.

さらに接着性等の二次加工性も向上している。したがっ
て本発明のセラコラ硬化体は住宅、倉庫等の建設材料と
して利用されるほか、一般産業資材としても有利に用い
ることができる。
Furthermore, secondary processability such as adhesion has also been improved. Therefore, the cured product of Ceracola of the present invention can be used advantageously as a construction material for houses, warehouses, etc., and also as a general industrial material.

次に、本発明を実施例により説明する。Next, the present invention will be explained by examples.

製造例 軽量球状セラコラの製造 0.5容量%酢酸水溶液601に2水セツコウ12kg
とβ型半水セツコウ600.9を加え混合してスラリー
を調製した。
Production example: Production of lightweight spherical Ceracola 12 kg of 2-water solution in 0.5% by volume acetic acid aqueous solution 601
and β-type hemihydrate 600.9 were added and mixed to prepare a slurry.

このスラリーを120°Cの飽和蒸気圧下でプロペラ型
攪拌羽根を用いてかきまぜながら約30分間水熱反応を
行なった。
A hydrothermal reaction was carried out for about 30 minutes while stirring this slurry using a propeller-type stirring blade under saturated steam pressure at 120°C.

水熱反応終了後、熱時、遠心分離機で固液分離して得ら
れた固状物は熱風乾燥機を用いて60℃で約8時間乾燥
処理を行ない、軽量球状α型半水セツコウを得た。
After the completion of the hydrothermal reaction, the solid material obtained by separating solid and liquid with a centrifuge during heating is dried at 60°C for about 8 hours using a hot air dryer to obtain a lightweight spherical α-type semi-hydrated slag. Obtained.

また、このα型半水セツコウの一部を電気炉を用いて5
00°Cで3時間焼成して軽量球状無水セラコラを得た
In addition, a part of this α-type semi-water slag was produced using an electric furnace.
After firing at 00°C for 3 hours, lightweight spherical anhydrous Ceracola was obtained.

得られた軽量球状セラコラはいずれも平均直径250μ
、かさ密度0.10g/Cr1tであった。
The obtained lightweight spherical ceracola each had an average diameter of 250 μm.
, and the bulk density was 0.10 g/Cr1t.

実施例 1 軽量球状α型手水セツコウ460gに水1800mlを
加えてスラリーとなし、このスラリーを抄造面30cI
rL×30crILで40メツシユの金網をもつ抄造型
枠に流し込み、抄造圧縮成形し、水和硬化後脱型して6
0℃の熱風乾燥器で乾燥して板状の軽量セラコラ成形体
を得た。
Example 1 1,800 ml of water was added to 460 g of a lightweight spherical α-type hand wash to make a slurry, and this slurry was applied to a papermaking surface of 30 cI.
It was poured into a papermaking mold having a wire mesh of 40 meshes with rL x 30crIL, and then subjected to papermaking compression molding. After hydration and hardening, the mold was removed.
It was dried in a hot air dryer at 0°C to obtain a plate-shaped lightweight Ceracola molded body.

この成形体の比重2曲げ強度、吸水率を表−1の屑1に
比較例として示す。
The specific gravity 2 bending strength and water absorption rate of this molded body are shown in Table 1, Scrap 1, as a comparative example.

次に、この成形体に過酸化ベンゾイル1重量パーセント
を含むメタクリル酸メチルを含浸量を変えて含浸し、こ
のものをアルミニウムはくで包み80℃に保持した熱風
乾燥器中で4時間放置し重合を行なわせた。
Next, this molded body was impregnated with varying amounts of methyl methacrylate containing 1% by weight of benzoyl peroxide, and this body was wrapped in aluminum foil and left in a hot air dryer kept at 80°C for 4 hours to polymerize. was made to do so.

得られた結果を表−1の42〜/16.5に示す。The obtained results are shown in Table 1 from 42 to /16.5.

。 含浸率−硬化体1量−成形体1量成形体重量 ※吸水率 20℃捌仲に24時司浸漬後の重量増加率実
施例 2 実施例1で用いたと同じ成形体に湿気硬化形ポリウレタ
ン樹脂を含浸し、24時間放置して硬化体を得た。
. Impregnation rate - 1 weight of cured body - 1 weight of molded body Molding weight *Water absorption rate Weight increase rate after 24 hour immersion in a 20°C solution Example 2 Moisture-curing polyurethane resin was added to the same molded body as used in Example 1. was impregnated and left to stand for 24 hours to obtain a cured product.

結果を表−2の應6に示す。実施例 3 実施例1で用いたと同じ成形体に融点63℃。The results are shown in Table 6 of Table 2. Example 3 The same molded body used in Example 1 had a melting point of 63°C.

83℃のワックスを90’Cに加熱して含浸し、冷却し
て硬化体を得た。
Wax at 83° C. was heated to 90° C. for impregnation, and then cooled to obtain a cured product.

結果を表−2の/I67 、 /168に示す。The results are shown in /I67 and /168 of Table 2.

Claims (1)

【特許請求の範囲】 1 直径0.01〜1011Li、かさ密度0.02〜
0.8g/−の軽量球状セラコラを主材とする原料から
得られる成形体に含浸性物質を含浸、硬化してなるセラ
コラ硬化体。 2 軽量球状セラコラがα型半水セツコウ、可溶性無水
セツコウおよび不溶性無水セラコラから選択されたもの
である特許請求の範囲第1項記載のセラコラ硬化体。 3 含浸性物質が重合性単量体2重合性プレポリマー、
熱硬化性樹脂、熱可塑性樹脂、ワックス。 アスファルト、イオウおよび金属よりなる群から選ばれ
た少なくとも1種の物質である特許請求の範囲第1項記
載のセラコラ硬化体。
[Claims] 1. Diameter 0.01~1011Li, bulk density 0.02~
A cured Ceracola product obtained by impregnating and curing a molded product obtained from a raw material mainly consisting of 0.8 g/- lightweight spherical Ceracola with an impregnating substance. 2. The cured body of Ceracola according to claim 1, wherein the lightweight spherical Ceracola is selected from α-type hemihydrate, soluble anhydrous, and insoluble anhydrous Ceracola. 3 The impregnating substance is a polymerizable monomer dipolymerizable prepolymer,
Thermosetting resins, thermoplastic resins, waxes. The cured body of Ceracola according to claim 1, which is at least one substance selected from the group consisting of asphalt, sulfur, and metal.
JP6230278A 1978-05-26 1978-05-26 hardened body Expired JPS5842151B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6230278A JPS5842151B2 (en) 1978-05-26 1978-05-26 hardened body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6230278A JPS5842151B2 (en) 1978-05-26 1978-05-26 hardened body

Publications (2)

Publication Number Publication Date
JPS54154423A JPS54154423A (en) 1979-12-05
JPS5842151B2 true JPS5842151B2 (en) 1983-09-17

Family

ID=13196193

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6230278A Expired JPS5842151B2 (en) 1978-05-26 1978-05-26 hardened body

Country Status (1)

Country Link
JP (1) JPS5842151B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7188695B2 (en) * 2018-12-19 2022-12-13 平太郎 木戸 Anhydrous gypsum manufactured molding and manufacturing method thereof

Also Published As

Publication number Publication date
JPS54154423A (en) 1979-12-05

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