JPH06141671A - Inorganic porous material - Google Patents

Inorganic porous material

Info

Publication number
JPH06141671A
JPH06141671A JP4301253A JP30125392A JPH06141671A JP H06141671 A JPH06141671 A JP H06141671A JP 4301253 A JP4301253 A JP 4301253A JP 30125392 A JP30125392 A JP 30125392A JP H06141671 A JPH06141671 A JP H06141671A
Authority
JP
Japan
Prior art keywords
inorganic porous
alc
porous material
soil
carbonation
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Withdrawn
Application number
JP4301253A
Other languages
Japanese (ja)
Inventor
Masaru Nomura
野村  勝
Masanori Tanabe
正紀 田邉
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 Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP4301253A priority Critical patent/JPH06141671A/en
Publication of JPH06141671A publication Critical patent/JPH06141671A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05DINORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D9/00Other inorganic fertilisers

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Cultivation Of Plants (AREA)
  • Porous Artificial Stone Or Porous Ceramic Products (AREA)

Abstract

PURPOSE:To provide the inorganic porous soil jor agricultural and horticultural uses capable of being utilized as siliceous fertilizer, soil-improving agent, slope face-greening soil, seedling-cultivating soil, horticultural soil, etc., by quickly reducing the strong alkalinity of ALC, while holding the excellent properties of the ALC. CONSTITUTION:This method for producing the inorganic porous material having a pH of <=9.6 is characterized by subjecting an inorganic porous material and ALC containing quartz and a pH of <=9.6 to a carbonization treatment.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、園芸用土や土壌改良剤
等として利用可能である無機質多孔体に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an inorganic porous material which can be used as a horticultural soil, a soil improving agent and the like.

【0002】[0002]

【従来の技術】多孔質珪酸カルシウム水和物を主成分と
する軽量気泡コンクリート(以下ALCと略称する)
は、建材や断熱材として多用されていると共に、その端
材は石英を含有することによる適当な強度、多孔体であ
ることから得られる見かけ比重の小ささ、透水性、保水
性、通気性などの特徴から、粉砕して例えば園芸用土、
土壌改良剤として利用されている。
2. Description of the Related Art Light-weight cellular concrete (hereinafter abbreviated as ALC) whose main component is porous calcium silicate hydrate
Is widely used as a building material and heat insulating material, and the end material has appropriate strength due to containing quartz, and the small apparent specific gravity obtained from being a porous body, water permeability, water retention, air permeability, etc. From the characteristics of, crush and for example garden soil,
It is used as a soil conditioner.

【0003】[0003]

【発明が解決しようとする課題】しかし、ALCはpH
が10以上もあり強アルカリ性であるため、ALC粉末
を珪酸質肥料や土壌改良剤等として利用する場合、局部
的に使用したり、大量に混入させると、アルカリが土壌
に悪影響を及ぼし植物の成育が阻害されるので、その使
用には細心の注意が必要である。
However, ALC has a pH value.
Since it has a strong alkalinity of 10 or more, when ALC powder is used as a siliceous fertilizer or a soil conditioner, if it is used locally or mixed in a large amount, the alkali will adversely affect the soil and the growth of plants. Since it is inhibited, it must be used with extreme caution.

【0004】このため、塩酸、硝酸などを用いた酸処理
を行うことによってALCのアルカリ性を低減させる方
法が考えうるが、このような方法では石英が分解される
こともあるため、適度な強度が失われやすい。従って本
発明は、ALCの有する強度、見かけ比重の小ささ、透
水性、保水性、通気性といった特長を失わしめることな
く、低アルカリ化された無機質多孔体を提供することに
ある。
Therefore, a method of reducing the alkalinity of ALC by performing an acid treatment using hydrochloric acid, nitric acid or the like can be considered, but such a method may decompose the quartz, so that it has an appropriate strength. Easy to lose. Therefore, the present invention is to provide a low-alkali inorganic porous material without losing the characteristics of ALC such as strength, small apparent specific gravity, water permeability, water retention, and air permeability.

【0005】[0005]

【課題を解決するための手段】本発明は、pHが9.6
以下であり石英を含有する無機質多孔体、および軽量気
泡コンクリートを炭酸化処理することによって、pHが
9.6以下である無機質多孔体を得る方法である。ここ
でいうpHとは、得られた無機質多孔体1gに25℃の
イオン交換水100gを加え、3分間攪拌した後、25
℃の恒温槽中でpH計で測定した値をいう。
The present invention has a pH of 9.6.
It is a method of obtaining an inorganic porous body having a pH of 9.6 or less by carbonating an inorganic porous body containing quartz and a lightweight cellular concrete below. The pH referred to here is 25 g after adding 100 g of ion-exchanged water at 25 ° C. to 1 g of the obtained inorganic porous material and stirring for 3 minutes.
The value measured with a pH meter in a constant temperature bath at ℃.

【0006】本発明に使用するALCは、例えば珪酸質
原料と石灰質原料とを混合してスラリ−状にしたものを
そのまま高温高圧水蒸気養生、あるいは該スラリーに発
泡剤、起泡剤などの気泡生成剤をも混合したスラリ−状
物を型枠内で硬化した後、高温高圧水蒸気養生してなる
人工鉱物等を挙げることができる。前記ALC成分はゾ
ノトライト、トバモライト、ジャイロライト、フォシャ
ジャイト、ヒレブランダイト等であり、これらの成分の
うちいずれか1つを単独成分とするものでも、2種類以
上を混合成分とするものでもよく、CSHゲルや未反応
の珪酸質原料等を含有していても構わないが、これらの
成分とともに石英を含有しているものでなければならな
い。前記石英は理学X線回折装置によって、石英の10
1面(2θ=3.34)の回折強度をcps単位により
測定した場合、ピークが存在していることが必要であ
る。
The ALC used in the present invention is, for example, a slurry obtained by mixing a siliceous raw material and a calcareous raw material, and curing the slurry as it is under high temperature and high pressure steam, or generating bubbles such as a foaming agent and a foaming agent in the slurry. An artificial mineral obtained by curing a slurry-like material mixed with an agent in a mold and then curing it at high temperature and high pressure steam may be mentioned. The ALC component is xonotlite, tobermorite, gyrolite, foshaygit, hellebrandite, or the like, and any one of these components may be a single component or a mixture of two or more types. , CSH gel, unreacted siliceous raw material and the like may be contained, but quartz must be contained together with these components. The quartz is made of quartz by a physical X-ray diffractometer.
When the diffraction intensity of one surface (2θ = 3.34) is measured in cps unit, it is necessary that a peak be present.

【0007】このALCには、前記のALCの製造工程
で発生する不良品や、ビルや住宅等への建設中に発生す
るALC端材なども使用することができる。ALCの粒
径などの形状はとくに限定されず、無機質多孔体の用途
によって選択すれば良い。本発明の炭酸化処理は、公知
の方法を採用することができ、特に限定されるものでは
なく、その例としては炭酸ガス雰囲気中にALCを接触
させる方法や、炭酸ガスを溶解させた水中にALCを投
入する方法などがあげられるが、炭酸化処理を行ったA
LCのpHが9.6以下となるまで炭酸化処理を行う必
要がある。
As the ALC, it is possible to use a defective product generated in the manufacturing process of the ALC, an ALC scrap produced during the construction of a building, a house or the like. The shape such as the particle size of ALC is not particularly limited and may be selected depending on the use of the inorganic porous body. The carbonation treatment of the present invention can employ a known method and is not particularly limited, and examples thereof include a method of bringing ALC into contact with a carbon dioxide gas atmosphere, or a method in which carbon dioxide gas is dissolved in water. A method of introducing ALC and the like can be mentioned.
It is necessary to perform carbonation treatment until the pH of the LC becomes 9.6 or less.

【0008】ALCはpHが10.3以上である。AL
C炭酸化する際の炭酸化度、すなわち炭酸化処理後のA
LC中のカルシウム分に対する炭酸カルシウム含有率
と、pHの関係は図1に示す通りである。ある程度の炭
酸化度まではpHは急激に低下し、pHが9.6程度に
達するとさらに炭酸化を行ってもpHは殆ど低下しな
い。
ALC has a pH of 10.3 or higher. AL
C degree of carbonation during carbonation, that is, A after carbonation treatment
The relationship between the calcium carbonate content with respect to the calcium content in LC and pH is as shown in FIG. The pH drops sharply up to a certain degree of carbonation, and when the pH reaches about 9.6, the pH hardly drops even if carbonation is further performed.

【0009】また、pHが9.6以下となるまで炭酸化
処理を行えば、炭酸化度は40%まで進行し、本発明の
無機質多孔体の実質的なpHも低減される。pHが9.
6を越える値であると、炭酸化の度合いが十分でなく、
本発明の無機質多孔体の用途が著しく限定される。
Further, if the carbonation treatment is carried out until the pH becomes 9.6 or less, the carbonation degree advances to 40%, and the substantial pH of the inorganic porous material of the present invention is also reduced. pH is 9.
If the value exceeds 6, the degree of carbonation is not sufficient,
The use of the inorganic porous material of the present invention is extremely limited.

【0010】[0010]

【図1】さらに前記方法によって得られる無機質多孔体
は、もとのALCの多孔体の形状を維持していると、無
機質多孔体を使用する際に、ALCの持つ特長を十分生
かすことができ好ましい。本発明の無機質多孔体は農・
園芸土や土壌改良剤、法面緑化用土、植栽用土、育苗培
土、園芸培土に使用することが可能である。
FIG. 1 shows that if the inorganic porous material obtained by the above method maintains the shape of the original porous material of ALC, the characteristics of ALC can be fully utilized when the inorganic porous material is used. preferable. The inorganic porous material of the present invention is
It can be used as horticultural soil, soil conditioner, slope greening soil, planting soil, nursery soil, and horticultural soil.

【0011】[0011]

【作用】以上の様な構成にすることにより、ALCと接
触する炭酸ガスがALCを炭酸化され、カルシウム分が
炭酸カルシウムとなるため、pHが実質的に下がるの
で、植物等へ本発明の無機質多孔体を使用しても悪影響
を与えることが無い。
With the above-mentioned constitution, the carbon dioxide gas contacting with ALC is carbonated in ALC and the calcium content becomes calcium carbonate, so that the pH is substantially lowered. Even if a porous body is used, it does not have a bad influence.

【0012】[0012]

【実施例】以下に、実施例、比較例を用いて本発明をさ
らに詳しく説明する。実施例、比較例に示すpH、石英
の結晶性及び炭酸化度は、以下の方法で測定した。 pH 得られた無機質多孔体1gに25℃のイオン交換水10
0gを加え、3分間攪拌した後、25℃の恒温槽中でp
H計で測定した。
EXAMPLES The present invention will be described in more detail below with reference to examples and comparative examples. The pH, the crystallinity of quartz and the carbonation degree shown in Examples and Comparative Examples were measured by the following methods. pH 1 g of the obtained inorganic porous material was added with ion-exchanged water 10 at 25 ° C.
After adding 0 g and stirring for 3 minutes, p in a constant temperature bath at 25 ° C.
It was measured with an H meter.

【0013】石英の結晶の有無 得られた無機質多孔体の理学X線回折装置によって、石
英の101面(2θ=3.34)の回折強度をcps単
位により測定した。 炭酸化度 得られた無機質多孔体を塩酸と反応させ、発生した炭酸
ガス量により炭酸化度を測定した。(ALC中のカルシ
ウム成分を完全に炭酸カルシウムとした状態を炭酸化度
100%とした。)
Presence of Quartz Crystals The physical intensity of the obtained inorganic porous material was measured by a physical X-ray diffractometer to measure the diffraction intensity of 101-face (2θ = 3.34) of quartz in cps unit. Carbonation degree The obtained inorganic porous material was reacted with hydrochloric acid, and the carbonation degree was measured by the amount of carbon dioxide gas generated. (The state where the calcium component in ALC was completely calcium carbonate was defined as 100% carbonation.)

【0014】[0014]

【参考例】ビル建設現場で発生したALC端材を回収
し、クラッシャーで潰してから、中の鉄筋を引き抜いた
のち、ハンマーミルで粗粉砕した。このようにして得た
粗粉砕物をふるい分けて、直径が2.0mm以下の粉状
ALCを得、これを110℃で恒量となるまで乾燥させ
た。
[Reference Example] ALC mill ends generated at a building construction site were collected, crushed by a crusher, the reinforcing bars in the inside were pulled out, and then coarsely crushed by a hammer mill. The coarsely pulverized product thus obtained was sieved to obtain a powdery ALC having a diameter of 2.0 mm or less, which was dried at 110 ° C. until a constant weight was obtained.

【0015】この粉状ALCは、トバモライトを主成分
とする珪酸質カルシウムからなり、X線回折と蛍光X線
分析によると、Ca/Siは0.58であった。また、
見かけ比重は0.65程度であり、保水率は75%程度
であった。さらに、この粉体のpH、101面のX線回
折強度、及び炭酸化度を表1に示す。
The powdery ALC was composed of siliceous calcium containing tobermorite as a main component, and Ca / Si was 0.58 by X-ray diffraction and fluorescent X-ray analysis. Also,
The apparent specific gravity was about 0.65, and the water retention rate was about 75%. Table 1 shows the pH, X-ray diffraction intensity of the 101st surface, and carbonation degree of this powder.

【0016】[0016]

【実施例1】温度計、ガス吹き込み管、還流冷却器を備
えた三ッ口フラスコに蒸留水80g、参考例で得られた
粉状ALC20gを入れ、マグネチックスターラーでに
炭酸ガスを吹き込み飽和させのち、pHを4.4程度に
調整した溶液に参考例で攪拌機しながら30℃に昇温
後、炭酸ガスを流速500cc/minで供給し、30
℃で攪拌下に5時間反応させた。反応生成物からALC
粉をろ別し、110℃で乾燥することによって本発明の
無機質多孔体を得た。この無機質多孔体のpH、101
面のX線回折強度、及び炭酸化度を表1に示す。
Example 1 80 g of distilled water and 20 g of the powdery ALC obtained in the reference example were put into a three-necked flask equipped with a thermometer, a gas blowing tube, and a reflux condenser, and carbon dioxide gas was blown into the magnetic stirrer to saturate it. After that, the temperature of the solution adjusted to about 4.4 was raised to 30 ° C. with a stirrer in the reference example, and carbon dioxide was supplied at a flow rate of 500 cc / min to give
The reaction was carried out at 0 ° C. under stirring for 5 hours. Reaction product to ALC
The powder was filtered off and dried at 110 ° C. to obtain the inorganic porous material of the present invention. PH of this inorganic porous material, 101
Table 1 shows the X-ray diffraction intensity and the carbonation degree of the surface.

【0017】見かけ比重は0.63、保水率は75%で
あり、参考例のものとほぼ同じであった。さらに、本実
施例で得られた無機質多孔体を直径10cmのシャーレ
に適量入れ水を適量入れ、小松菜の種を50個まいた
後、室温(20℃)の部屋に10日間置き、発芽状態と
その後の生育状況を観察した。その結果、3日後の発芽
率は90%程度であり、7日後には3.5cmまで成長
し、その後も順調に成長した。
The apparent specific gravity was 0.63 and the water retention rate was 75%, which were almost the same as those of the reference example. Furthermore, an appropriate amount of the inorganic porous material obtained in this example was placed in a petri dish having a diameter of 10 cm, water was added in an appropriate amount, 50 seeds of Komatsuna were seeded, and the seeds were placed in a room at room temperature (20 ° C.) for 10 days to obtain a germinated state. The subsequent growth situation was observed. As a result, the germination rate after 3 days was about 90%, after 7 days it had grown to 3.5 cm, and after that it had grown satisfactorily.

【0018】[0018]

【実施例2】実施例1において、炭酸化処理を60℃で
行った以外は同様の方法によって本発明の無機質多孔体
を得た。得られた無機質多孔体について、pH、101
面のX線回折強度、及び炭酸化度を測定した結果を表1
に示す。
Example 2 An inorganic porous material of the present invention was obtained by the same method as in Example 1, except that the carbonation treatment was performed at 60 ° C. About the obtained inorganic porous body, pH, 101
Table 1 shows the results of measuring the X-ray diffraction intensity and the carbonation degree of the surface.
Shown in.

【0019】[0019]

【実施例3】実施例1において、炭酸化処理を60℃、
反応時間を3時間で行った以外は同様の方法によって本
発明の無機質多孔体を得た。得られた無機質多孔体につ
いて、pH、101面のX線回折強度、及び炭酸化度を
測定した結果を表1に示す。見かけ比重は0.66、保
水率は81%であり、参考例のものと大差はなかった。
[Example 3] In Example 1, the carbonation treatment was carried out at 60 ° C.
An inorganic porous material of the present invention was obtained by the same method except that the reaction time was 3 hours. Table 1 shows the results of measuring the pH, the X-ray diffraction intensity of the 101 plane, and the carbonation degree of the obtained inorganic porous body. The apparent specific gravity was 0.66 and the water retention rate was 81%, which was not much different from that of the reference example.

【0020】[0020]

【実施例4】オートクレーブに参考例で得られた粉状A
LCを20部と蒸留水15部を入れて脱気後、炭酸ガス
をゲージ圧1.2kg/cm2 圧入し、1日間反応させ
た後、110℃で乾燥させることにより、本発明の無機
質多孔体を得た。得られた無機質多孔体について、p
H、101面のX線回折強度、及び炭酸化度を測定した
結果を表1に示す。
[Example 4] Powder A obtained in Reference Example in an autoclave
After 20 parts of LC and 15 parts of distilled water were introduced and degassed, carbon dioxide gas was introduced under a gauge pressure of 1.2 kg / cm 2 and reacted for 1 day, followed by drying at 110 ° C. to give the inorganic porous material of the present invention. Got the body For the obtained inorganic porous material, p
Table 1 shows the results of measuring the X-ray diffraction intensity of H, the 101st plane, and the carbonation degree.

【0021】さらに、実施例1と同様の方法で小松菜の
生育状況を観察した。その結果、3日後の発芽率は90
%程度であり、7日後には3.1cmまで成長し、その
後も順調に成長した。
Furthermore, the growth of Komatsuna was observed in the same manner as in Example 1. As a result, the germination rate after 3 days was 90.
% After about 7 days, the growth was 3.1 cm after 7 days, and the growth was good thereafter.

【0022】[0022]

【比較例1】実施例1において、炭酸化処理を30℃、
反応時間を3時間で行った以外は同様の方法によって無
機質多孔体を得た。得られた無機質多孔体について、p
H、101面のX線回折強度、及び炭酸化度を測定した
結果を表1に示す。さらに、実施例1と同様の方法で小
松菜の生育状況を観察した。その結果、3日後の発芽率
は90%程度であり、7日後には3.1cmまで成長
し、その後葉先が丸くなり、成長はほとんど停止した。
[Comparative Example 1] In Example 1, the carbonation treatment was carried out at 30 ° C.
An inorganic porous material was obtained by the same method except that the reaction time was 3 hours. For the obtained inorganic porous material, p
Table 1 shows the results of measuring the X-ray diffraction intensity of H, the 101st plane, and the carbonation degree. Furthermore, the growth of Komatsuna was observed in the same manner as in Example 1. As a result, the germination rate after 3 days was about 90%, after 7 days it had grown to 3.1 cm, after which the leaf tips were rounded and growth almost stopped.

【0023】[0023]

【比較例2】実施例1において、炭酸化処理を80℃、
反応時間を1時間で行った以外は同様の方法によって無
機質多孔体を得た。得られた無機質多孔体について、p
H、101面のX線回折強度、及び炭酸化度を測定した
結果を表1に示す。
[Comparative Example 2] In Example 1, the carbonation treatment was carried out at 80 ° C,
An inorganic porous material was obtained by the same method except that the reaction time was 1 hour. For the obtained inorganic porous material, p
Table 1 shows the results of measuring the X-ray diffraction intensity of H, the 101st plane, and the carbonation degree.

【0024】[0024]

【比較例3】実施例1において、炭酸化処理を30℃、
反応時間を1時間で行った以外は同様の方法によって無
機質多孔体を得た。得られた無機質多孔体について、p
H、101面のX線回折強度、及び炭酸化度を測定した
結果を表1に示す。
[Comparative Example 3] In Example 1, the carbonation treatment was conducted at 30 ° C.
An inorganic porous material was obtained by the same method except that the reaction time was 1 hour. For the obtained inorganic porous material, p
Table 1 shows the results of measuring the X-ray diffraction intensity of H, the 101st plane, and the carbonation degree.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【発明の効果】本発明の無機質多孔体は、石英を有する
ことにより適当な強度を有する等、ALCの持つ特徴を
失うことなく、ALCの強アルカリ性を短時間で簡便の
方法により低減されており、例えば園芸用土、充填材等
の広用途に利用しうる無機質多孔体を提供することが可
能となる。
INDUSTRIAL APPLICABILITY The inorganic porous material of the present invention has a suitable strength due to having quartz, and the strong alkalinity of ALC is reduced by a simple method in a short time without losing the characteristics of ALC. Thus, it becomes possible to provide an inorganic porous material that can be used for a wide range of applications such as garden soil and fillers.

【図面の簡単な説明】[Brief description of drawings]

【図1】炭酸化度とpH値の関係を示したグラフであるFIG. 1 is a graph showing the relationship between carbonation degree and pH value.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 pHが9.6以下であり、石英を含有す
る無機質多孔体
1. An inorganic porous material having a pH of 9.6 or less and containing quartz.
【請求項2】 軽量気泡コンクリートを炭酸化処理する
ことによって、pHが9.6以下である石英含有の無機
質多孔体を得る方法
2. A method for obtaining a quartz-containing inorganic porous body having a pH of 9.6 or less by carbonating a lightweight cellular concrete.
JP4301253A 1992-11-11 1992-11-11 Inorganic porous material Withdrawn JPH06141671A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4301253A JPH06141671A (en) 1992-11-11 1992-11-11 Inorganic porous material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4301253A JPH06141671A (en) 1992-11-11 1992-11-11 Inorganic porous material

Publications (1)

Publication Number Publication Date
JPH06141671A true JPH06141671A (en) 1994-05-24

Family

ID=17894606

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4301253A Withdrawn JPH06141671A (en) 1992-11-11 1992-11-11 Inorganic porous material

Country Status (1)

Country Link
JP (1) JPH06141671A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007306844A (en) * 2006-05-18 2007-11-29 Kawasaki Plant Systems Ltd Method for producing greening material using waste material, and greening material
JP7298986B1 (en) * 2023-03-18 2023-06-27 クリオン株式会社 Method for producing silicic fertilizer
US11897824B2 (en) * 2020-01-30 2024-02-13 Dong Chan Koo Method of preparing activated mineral solution

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007306844A (en) * 2006-05-18 2007-11-29 Kawasaki Plant Systems Ltd Method for producing greening material using waste material, and greening material
US11897824B2 (en) * 2020-01-30 2024-02-13 Dong Chan Koo Method of preparing activated mineral solution
JP7298986B1 (en) * 2023-03-18 2023-06-27 クリオン株式会社 Method for producing silicic fertilizer

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