JPS5841760A - Fibrous hillebrandite and manufacture - Google Patents

Fibrous hillebrandite and manufacture

Info

Publication number
JPS5841760A
JPS5841760A JP13609881A JP13609881A JPS5841760A JP S5841760 A JPS5841760 A JP S5841760A JP 13609881 A JP13609881 A JP 13609881A JP 13609881 A JP13609881 A JP 13609881A JP S5841760 A JPS5841760 A JP S5841760A
Authority
JP
Japan
Prior art keywords
fibrous
crystalline
calcium silicate
silicate hydrate
present
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.)
Granted
Application number
JP13609881A
Other languages
Japanese (ja)
Other versions
JPH0216255B2 (en
Inventor
清水 幸壽
雄一 土井
松尾 俊次
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.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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 Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP13609881A priority Critical patent/JPS5841760A/en
Publication of JPS5841760A publication Critical patent/JPS5841760A/en
Publication of JPH0216255B2 publication Critical patent/JPH0216255B2/ja
Granted legal-status Critical Current

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  • Manufacture, Treatment Of Glass Fibers (AREA)
  • Inorganic Fibers (AREA)

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】 本発明は結晶長50μm以上の結晶性ヒレプランダイト
からなる繊維状ヒレプランダイト及び七の製造方法に関
する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fibrous fillet prandite made of crystalline fillet prandite having a crystal length of 50 μm or more and a manufacturing method according to item 7.

従来、無機繊維の代表的なものとしては石綿があり、こ
れは繊―長が長く工業的有意性の高いものであるが、天
然Ki!するものであるため将来枯渇することが予掬さ
糺、また近年発8性物質として疑われ、環境保全上野1
1.<ない材料と考えられるに至っている。石−以外の
無機繊維として一般的に知られているプラス繊維やロッ
クウールは断熱材として使用されているものの、耐アル
カリ性に劣ることから、フィラー、補強材としては必す
しも万能でない。またセフイックファイバーは種々優れ
た特性を有する反自、あまりにも高価でありすぎるため
補強材、フィラー等の汎用の工業材料として実用に撫さ
れない。
Traditionally, asbestos has been a typical inorganic fiber, which has long fibers and is of high industrial significance, but natural Ki! It is predicted that it will be depleted in the future, and it has been suspected that it has been produced in recent years as a chemical substance, and has been designated as an environmental conservation Ueno 1 substance.
1. It has come to be considered a material that does not exist. Although plastic fibers and rock wool, which are generally known as inorganic fibers other than stone, are used as heat insulating materials, they are not necessarily versatile as fillers and reinforcing materials because of their poor alkali resistance. Although safe fibers have various excellent properties, they are also too expensive to be put into practical use as general-purpose industrial materials such as reinforcing materials and fillers.

一万、ヒレプ□ランダイトはけい酸質原料と石灰質鳳P
#な使用し、比較的容asvc合成できる物質であり、
しかもその原料は我が国に豊富\に存在し、安価に入手
可能□であり、その特性はけい酸カルシウムを主体とす
る鉱物であるため、lFr熱性に優れ、水との1a11
I性も優れていて七の合成物の繊維化については従来い
くつかの試みが°なされてきた。
10,000, Hirepu □ Landite is a silicic acid raw material and a calcareous thorn P
It is a substance that can be synthesized in a relatively small amount using ASVC,
Moreover, its raw materials are abundant in Japan and can be obtained at low cost.Its properties are that it is a mineral mainly composed of calcium silicate, so it has excellent lFr thermal properties, and has a 1a11 compatibility with water.
Several attempts have been made in the past to make fibers from synthetic materials with excellent I properties.

例えばCaO−8101−H2Oの三成分系にアルカリ
その他の11!)lIlIIE1JIJ愉を加え、温度
、圧力、時間、組成等について検討するもヒレプシンダ
イトテ長い繊維材料な作ることはできなかった。
For example, in the ternary system of CaO-8101-H2O, alkali and other 11! )lIlIIE1JIJYU and investigated temperature, pressure, time, composition, etc., but it was not possible to make a long fiber material.

現在、工業的に製造可能なヒレプシンダイトは結晶長&
umm度の黴細なもので凝集しゃすく濾過抵抗性が大な
る欠点を有している。
At present, the industrially produced hylepsyndite has a crystal length of
It is a moldy substance with a microscopic degree of flocculation and has a major drawback of resistance to filtration.

本発明者らは予め高銀高圧に設定された熱アルカリ水中
にけい酸カルシウム水和物含有物を主体とするけい酸カ
ルシクム水和物を加え水鶏合成を行うという全く新規な
水熱合成技術によって結晶、長の大半が50μm以上で
ある結晶性ヒレプシンダイトな主体とする繊維状ヒレプ
ランダイトを得ることが出来た。
The present inventors used a completely new hydrothermal synthesis technique in which calcium silicate hydrate, mainly containing calcium silicate hydrate, was added to hot alkaline water preset to high silver and high pressure to perform water synthesis. It was possible to obtain fibrous hireplandite, which is mainly composed of crystalline hirepshindite, in which most of the crystal lengths are 50 μm or more.

本発羽品は化学分析の結果、その化学成分はほとんどが
CaOg Sing @ HIOからなる化合物で、そ
の化学組成式はCa1SiO^であり、x+1III折
の結果、ヒレプシンダイトと固定された。また、熱分析
の結果、市場に出廻っている代表的なけい酸カルシウム
の一つであるトバモライトよりも熱安定性に優れ1いる
ので断熱材、耐熱材として使用でき、しかもr過性が良
好であり、嵩高なので合成樹脂成形品のフィラーや葡強
材としても使用できるものであることを見出し1本発明
を完成させるに至った。
As a result of chemical analysis of this feather product, its chemical components were mostly a compound consisting of CaOg Sing @ HIO, its chemical composition formula was Ca1SiO^, and as a result of x+1III folding, it was fixed as hylepsyndite. Additionally, as a result of thermal analysis, it has better thermal stability than tobermorite, which is one of the typical calcium silicate materials on the market1, so it can be used as a heat insulating material and a heat resistant material, and has good r-permeability. Because of its bulk, the inventors discovered that it could be used as a filler for synthetic resin molded products and as a reinforcing material, leading to the completion of the present invention.

すなわち、本発明のIIIの発明は結晶長50μm以上
の結晶性ヒレプシンダイトからなることを轡黴とする繊
維状ヒレプシンダイトである。
That is, the third invention of the present invention is a fibrous hylepsyndite which is composed of crystalline hylepsyndite with a crystal length of 50 μm or more.

!1!2の発明は予め高温高圧に設定された熱アルカリ
水中へけい酸カルシウム水和物を加え水熱反応せしめ繊
維状の結晶性ヒレプランダイトを生成せしめることをq
#黴とする繊維状ヒレプランダイトの製造方法である。
! The invention of 1 and 2 involves adding calcium silicate hydrate to hot alkaline water preset at high temperature and high pressure to cause a hydrothermal reaction to produce fibrous crystalline finprandite.
#This is a method for producing fibrous finprandite as mold.

ここで、熱アルカリ水のアルカリとはアルカリ金属の水
酸化物、水酸化ナトリウム、水酸化カリウム等のアルカ
リ物質を言い、アルカリ濃度として0.5〜4モへ4あ
れば充分である。
Here, the alkali of hot alkaline water refers to alkaline substances such as alkali metal hydroxides, sodium hydroxide, potassium hydroxide, etc., and an alkali concentration of 0.5 to 4 mo is sufficient.

けい酸カルシウム水和物とはけい酸質物声と石灰質物質
&−’I@へ高温高圧の飽和蒸気圧養生によって祷られ
るコンクリート、モルタル、スラリー。
Calcium silicate hydrate is a material used in concrete, mortar, and slurry that is cured by saturated vapor pressure at high temperatures and pressures.

オートクレーブ養生した気泡コンクリート等CaO−8
101−Hρ 系の物質な言い、出発物質としてのけい
酸カルシウム水和物のCab/ 81偽モル比は1〜3
あれば充分である。水熱反応系における熱アルカリ水と
出発物質としてのけい酸カルシクム水和吻の混合割合は
任意であるが、けい酸カルシクム水和物1重量部に対し
て熱アルカリ水約10重量部以上好ましくは100重量
部以上用いれば充分である。
Autoclave-cured aerated concrete, etc. CaO-8
101-Hρ system substance, the Cab/81 pseudomolar ratio of calcium silicate hydrate as a starting material is 1 to 3.
It is enough. The mixing ratio of hot alkaline water and calcium silicate hydrate as a starting material in the hydrothermal reaction system is arbitrary, but preferably about 10 parts by weight or more of hot alkaline water per 1 part by weight of calcium silicate hydrate. It is sufficient to use 100 parts by weight or more.

この発明で言う水熱反応とは熱アルカリ水の飽和蒸気圧
−トにおいて結晶化反応を促進させることであり、繊維
状ヒレプランダイト結晶の形成に要する温度は200〜
300℃で充分である。
The hydrothermal reaction referred to in this invention refers to promoting the crystallization reaction at the saturated vapor pressure of hot alkaline water, and the temperature required to form fibrous hireplandite crystals is 200 to 200°C.
300°C is sufficient.

水熱反応終了1lII形分である繊維状ヒレプシンダイ
ト結晶は水中に懸濁したスラリー状として反応槽から散
出され、P別等により分離され、その乾燥物は白色の粉
状乃至フレーク状で水を害鳥に透過する繊維状物質であ
る。この繊維状物質は後述する実施例において示すよう
に極めて純度の高い結晶性ヒレプランダイトであり、耐
熱惟、耐アルカリ性に優れたものである。また結晶長5
0μm以上という繊維状物質であるため循強効釆のある
 5− フィラー、加護の担体、P過材、吸着剤等としても使用
することができる。
Completion of hydrothermal reaction 1l The fibrous hylepsyndite crystals, which are type II, are dispersed from the reaction tank as a slurry suspended in water, separated by P separation, etc., and the dried product is dissolved in water in the form of white powder or flakes. It is a fibrous substance that is permeable to harmful birds. As shown in the examples below, this fibrous material is extremely pure crystalline hireplandite and has excellent heat resistance and alkali resistance. Also, crystal length 5
Since it is a fibrous material with a diameter of 0 μm or more, it can also be used as a 5-filler with a cyclic effect, a protective carrier, a P filter material, an adsorbent, etc.

以下、本発’lな実施例により更に詳細に説明するが、
本発明はこれらの実施例に限定されるものではない。な
お実施例における一定条件は次の通りである。
Hereinafter, it will be explained in more detail using examples according to the present invention.
The present invention is not limited to these examples. Note that certain conditions in the examples are as follows.

(リ 化学成分 石灰の化学分析方法JIS R9011に準拠して一定
した。
(Chemical components were determined in accordance with JIS R9011, a chemical analysis method for lime.

(27#lf[ ゴム用配合剤の試験方法JIB R6220に準拠して
一定した。
(27 #lf [Test method for rubber compounding agents JIBR R6220).

(3)Xmll折 対@@Cu、フィルターN1、管電圧30KV、管電流
15mA、フルスケール計axoooeps、走査速度
2#度/分で一定した。
(3) Xmll ratio @@Cu, filter N1, tube voltage 30 KV, tube current 15 mA, full scale meter axooooeps, scanning speed constant at 2# degrees/min.

(4)水差熱分析 試料重量10mg、DTA範囲±1007AV、昇温速
度10℃/分で一定した。
(4) Hydraulic thermal analysis The sample weight was 10 mg, the DTA range was ±1007 AV, and the heating rate was constant at 10° C./min.

実施例1゜ + 6− 釧2イニングしたオートクレーブ内容積1500aJK
2モVjの水酸化ナトリウム水濠筐を内容積の約1/2
入れ密閉後250℃に加熱する。−万、ホワイトカーボ
ン(8i0. = 86%132重量部、消石灰(Ca
O=74%)68重量部、CaO/810t モル比中
2、水1000重量部の混合物を約90℃で5時間加熱
して作成した非晶質けい酸カルシウム水和物懸濁i[な
上記熱アルカリ水中へ加圧ポンプで内容積の約1/4入
れる。、zsocで5時間保持して水鶏反応させた後冷
却して内容−を礒出し、水洗P別後105±5℃で乾燥
した本発明品の化学成分。
Example 1゜+6- Autoclave with 2 innings of internal volume 1500aJK
Approximately 1/2 of the internal volume of the 2MoVj sodium hydroxide water moat enclosure
After putting it in and sealing it, heat it to 250℃. -10,000, white carbon (8i0. = 86% 132 parts by weight, slaked lime (Ca
A suspension of amorphous calcium silicate hydrate prepared by heating a mixture of 68 parts by weight (O=74%), 2 in CaO/810t molar ratio, and 1000 parts by weight of water at about 90°C for 5 hours [the above Pour about 1/4 of the internal volume into hot alkaline water using a pressure pump. The chemical components of the product of the present invention were kept for 5 hours in zsoc and reacted with water, cooled and the contents were extracted, washed with water and dried at 105±5°C.

組成式および嵩密度をls1表に、Xm1li折、示差
熱分析及び走査電子顯黴鏡観−結果を第1図〜第3図に
示した潰一 本発明品は@1表及び纂1図で明らかなように化学組成
式がCa18 IO6KB からなるヒレプランダイト
と同定された。本発明品の熱的挙動は第2図に示す如り
600℃近傍KIL熱ピークを電極するもので、脱水に
伴う熟眠Sはトバモライトに比較し1循めて小さく、耐
WIk材として優れた特性を有するものであった。−万
、本発明品の結晶形状は183図で明らかなように繊維
状で、その長さは大手が50μm以上で平均長さは10
0−であった。
The compositional formula and bulk density are shown in Table Is1, and the results of Xm1li analysis, differential thermal analysis, and scanning electron microscope observation are shown in Figures 1 to 3.The products of the present invention are shown in Table 1 and Figure 1. As is clear, the chemical composition was identified as hireprundite consisting of Ca18 IO6KB. As shown in Figure 2, the thermal behavior of the inventive product is such that the KIL thermal peak near 600°C is used as an electrode, and the deep sleep S due to dehydration is much smaller than that of tobermorite, making it an excellent property as a WIk-resistant material. It had a - As is clear from Figure 183, the crystalline shape of the product of the present invention is fibrous, with a length of 50 μm or more and an average length of 10 μm.
It was 0-.

本発明品は熱硬化性樹脂、熱硬化性樹脂のフィラー、F
jl材とし−Cf用できることを実験的に蓚かめた。
The products of the present invention are thermosetting resins, thermosetting resin fillers, F
It was experimentally confirmed that the JL material could be used for -Cf.

実施例2゜ 2モへ4の水酸化ナトリウム水溶i[を2モに/1の水
酸化カリウム水111[K置き換えて実施例1を繰返し
た結果、結晶ik50μm以上、平均長さ100μmの
結晶性ヒレプランダイトが得られた。
Example 2 As a result of repeating Example 1 by substituting 4 sodium hydroxide aqueous solution i[2 to 2 mo/1 potassium hydroxide aqueous 111 [K], crystallinity with crystal ik 50 μm or more and average length 100 μm was obtained. Hireprandite was obtained.

本発明品の1質特性は実施f11で得た発明品と同様で
あった。
The quality characteristics of the product of the present invention were similar to those of the product obtained in Example f11.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明品のXIm回折図、92図は示差熱分析
図、第3図はその顯黴鏡写真である。 普出願人 旭化成工業株式会社  9− 第1図 Hlレフ′ラシダイト 回才午角Cuk(2e deQ ) 第2因 5里 &   (’C)
FIG. 1 is an XIm diffraction diagram of the product of the present invention, FIG. 92 is a differential thermal analysis diagram, and FIG. 3 is a microscopic photograph thereof. General applicant: Asahi Kasei Industries, Ltd. 9- Fig. 1 Hl ref' Rashidite rotational meridional angle Cuk (2e deQ) 2nd cause 5ri &('C)

Claims (1)

【特許請求の範囲】 1、 結晶長50−以上の結晶性ヒレプランダイトから
なることを4I黴とする繊維状ヒレプランダイト 2、 予め高温高圧に設定されたアルカリ金属水酸化物
員度O,S〜4モに/lの熱アルカリ水中へCaO/S
 IO@%ル比1.5〜3のけい酸カルシウム水和物を
、加えて200−aoo cの飽和蒸気圧下に水熱反応
せしめ、繊維状の結晶性ヒレプランダイトな生成せしめ
ることケ4I徴とする繊維状ヒレプランダイトの製造方
[Scope of Claims] 1. Fibrous hireprundite, which is 4I mold, consisting of crystalline hireprundite with a crystal length of 50 or more. 2. Alkali metal hydroxide membership degree O, which is preset at high temperature and high pressure. CaO/S to 4 mo/l of hot alkaline water
Calcium silicate hydrate with an IO@% ratio of 1.5 to 3 is added and subjected to a hydrothermal reaction under a saturated vapor pressure of 200-aoo c to produce fibrous crystalline fillerprandite. Method for producing fibrous finprandite
JP13609881A 1981-09-01 1981-09-01 Fibrous hillebrandite and manufacture Granted JPS5841760A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13609881A JPS5841760A (en) 1981-09-01 1981-09-01 Fibrous hillebrandite and manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13609881A JPS5841760A (en) 1981-09-01 1981-09-01 Fibrous hillebrandite and manufacture

Publications (2)

Publication Number Publication Date
JPS5841760A true JPS5841760A (en) 1983-03-11
JPH0216255B2 JPH0216255B2 (en) 1990-04-16

Family

ID=15167214

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13609881A Granted JPS5841760A (en) 1981-09-01 1981-09-01 Fibrous hillebrandite and manufacture

Country Status (1)

Country Link
JP (1) JPS5841760A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6471783A (en) * 1987-09-03 1989-03-16 Appleton Paper Inc Thermal response recording material
JPH05185740A (en) * 1992-01-08 1993-07-27 Fuji Photo Film Co Ltd Recording material

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20220083699A (en) 2019-10-17 2022-06-20 고리츠다이가쿠호진 요코하마시리츠다이가쿠 Methods for evaluating drug toxicity

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5520291A (en) * 1978-06-03 1980-02-13 Turner & Newall Ltd Production of fine fibrous tricalcium silicate dihydrate

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5520291A (en) * 1978-06-03 1980-02-13 Turner & Newall Ltd Production of fine fibrous tricalcium silicate dihydrate

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6471783A (en) * 1987-09-03 1989-03-16 Appleton Paper Inc Thermal response recording material
JPH05185740A (en) * 1992-01-08 1993-07-27 Fuji Photo Film Co Ltd Recording material

Also Published As

Publication number Publication date
JPH0216255B2 (en) 1990-04-16

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