JPS63282116A - Granular calcium hydroxide and manufacture thereof - Google Patents

Granular calcium hydroxide and manufacture thereof

Info

Publication number
JPS63282116A
JPS63282116A JP11633487A JP11633487A JPS63282116A JP S63282116 A JPS63282116 A JP S63282116A JP 11633487 A JP11633487 A JP 11633487A JP 11633487 A JP11633487 A JP 11633487A JP S63282116 A JPS63282116 A JP S63282116A
Authority
JP
Japan
Prior art keywords
slaked lime
aluminum silicate
calcium hydroxide
granular
montmorillonite
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
JP11633487A
Other languages
Japanese (ja)
Other versions
JPH054339B2 (en
Inventor
Sozo Nakazawa
中澤 壮三
Akira Takizawa
彰 滝澤
Takahide Kikuchi
隆秀 菊地
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.)
Yoshizawa Lime Industry Co Ltd
Original Assignee
Yoshizawa Lime 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 Yoshizawa Lime Industry Co Ltd filed Critical Yoshizawa Lime Industry Co Ltd
Priority to JP11633487A priority Critical patent/JPS63282116A/en
Publication of JPS63282116A publication Critical patent/JPS63282116A/en
Publication of JPH054339B2 publication Critical patent/JPH054339B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2/00Lime, magnesia or dolomite
    • C04B2/02Lime
    • C04B2/04Slaking
    • C04B2/06Slaking with addition of substances, e.g. hydrophobic agents ; Slaking in the presence of other compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)

Abstract

PURPOSE:To manufacture a granular calcium hydroxide which is not solidified for a long period and is excellent in breaking resistance in the water and under the ground by pressing and solidifying a mixture of the calcium hydroxide and specific colloidal aluminum silicate hydrate, and grinding and classifying the mixture. CONSTITUTION:78-97wt.% calcium hydroxide and 22-23wt.% colloidal aluminum silicate having >=8ml/2g degree of swelling (e.g., montmorillonite) are mixed, and the mixture is pressed, solidified, subsequently grinded and classified.

Description

【発明の詳細な説明】[Detailed description of the invention]

発明の目的 purpose of invention

【産業上の利用分野】[Industrial application field]

本発明は、改良された粒状消石灰とその製造方法に関す
る。 ここで1消石灰」とは、Ca(OH>2を主成分
とする石灰質の資材でおって、苦土消石灰を含み、農業
用、化学工業用、水処理用など種々の用途に向ける工業
資材を包括する。 [従来の技術1 消石灰は、粉末のままでは取扱いに不便である。 たとえば土壌に散布する際に、機械散布できず作業性が
悪いし、飛散しやすくて近隣に迷惑をかけたり、作業者
の安全衛生の観点からも注意を要する。 従って、消石
灰は粒状化することが望ましい。 しかし、消石灰を単に造粒しても、すぐ吸湿してしまい
、それとともに空気中の炭酸ガスと反応して炭酸カルシ
ウムが生成するため、固結しやすい。 固結しないまで
も、粒の表面は溶は難くなっているから、これを土壌に
散布しても仲々崩壊せず、使用効果が発揮されない。 粒の固結を防止し、崩壊性を高く保った粒状消石灰とし
て消石灰にベントナイトと植物性粘質物とを加えたもの
が提案された(特開昭58−194738>。 植物性
粘質物とは各種の天然のガム類をいい、そのエーテル化
誘導体も有用とされている。 しかし、輸入にまつ天然
物は廉価かつ安定な供給を望み難いし、それ自体はアル
カリ度に寄与しないという点でも不利益であるから、こ
のような材料を使用せずに、同様な効果を得たい。 [発明が解決しようとする問題点] 本発明の目的は、安価で入手しやすい副資材だけを使用
して、長期にわたり固化しない保存性と、水中または土
中での速やかな崩壊性を兼ねそなえた粒状消石灰と、そ
の製造方法を提供することにある。 発明の構成 [問題点を解決するための手段] 本発明の粒状消石灰は、消石灰78〜97重量%と膨潤
度8Inl/2g以上のコロイド性含水ケイ酸アルミニ
ウム3〜22重量%との緊密な混合物からなる。 ここで「膨潤度」とは、25℃の蒸留水100威中に2
gのサンプルを約20回に別けて落し、24時間後の見
掛容量を読む、いわゆるA、C。 C9法で測定された値である。 コロイド性含水ケイ酸アルミニウムの代表的なものは、
モンモリロナイト、またはそれを主成分とするNa型ベ
ントナイトである。 上記の粒状消石灰を製造する方法は、消石灰78〜97
重量%と膨潤度8d/2tj以上のコロイド性含水ケイ
酸アルミニウム、代表的には上記したモンモリロナイト
またはそれを主成分とするNa型ベントナイト3〜22
重量%とを混合し、プレスして、たとえば板状体とした
後、解砕し分級することからなる。 モンモリロナイトまたはNa型ベントナイトは、できる
だけ微粉末であることが好ましい。 また、あらかじめ
100〜200℃の温度に加熱して乾燥させて使用する
と、一層効果的であり、これは推奨すべき態様である。 [作 用] 前記した先行技術文献には、植物性粘質物とベントナイ
トの併用が不可欠であって、ベントナイト単独で使用し
て造粒した消石灰は、崩壊性が低いと記しである。 し
かし本発明者らの研究の結果、特定の高い膨潤性をもっ
たモンモリロナイトまたはNa型ベントナイトのような
コロイド性含水ケイ酸アルミニウムを用いることによっ
て、有機性粘結剤なしでも高い崩壊性および保存性をそ
なえた消石灰が造粒できることがわかったのである。 コロイド性含水ケイ酸アルミニウムの微粉末は、消石灰
の粉末と混合すると、その表面を被覆し、  −各粉末
粒子を隔てるように存在する。 それによって、消石灰
の粉末に環境中の水分ヤ炭醗ガスが接触して吸収され、
反応することを妨げるはたらきをする。 膨潤性が高いということは、吸湿力ないし吸水性が強い
ということを意味し、環境から消石灰が水分を吸収する
際に、コロイド性含水ケイ酸アルミニウムが水分を奪っ
てしまい、消石灰の吸湿は進まない。 このような作用があいまって、保存中の消石灰の吸湿は
ほとんどおこらず、炭酸ガスとの反応が防止され、粒子
の固結や個々の粒子の表面固化が抑制される。 一方、このようにして保存してきた粒状の消石灰を土壌
に散布すると、コロイド性含水ケイ酸アルミニウムが土
中の水分を激しく吸収して膨潤し、容積が膨張するから
、粒子中の消石灰の粉末がバラバラになる。 つまり、
容易に崩壊する。 上記のような効果を期待するためには、モンモリロナイ
トまたはそれを主成分とするNa型ベントナイトのよう
なコロイド性含水ケイ酸アルミニウムの膨潤度が8m/
2SF以上であることを要する。 また、消石灰との混合量が3重量%に足らないと効果が
なく、高い崩壊性は得られない。 多量に加えても効果
が飽和するし、過大になると、Ca  (OH)2の含
有量が低下してしまうため、22%を上限値とした。
The present invention relates to an improved granular slaked lime and a method for producing the same. Here, 1 slaked lime is a calcareous material whose main component is Ca(OH>2), which contains slaked limestone and is an industrial material for various uses such as agriculture, chemical industry, and water treatment. [Conventional technology 1] Slaked lime is inconvenient to handle in its powder form. For example, when spraying it on soil, it cannot be sprayed mechanically, making it difficult to work, and it easily scatters, causing a nuisance to neighbors. Care must also be taken from the standpoint of worker safety and health. Therefore, it is desirable to granulate slaked lime. However, even if slaked lime is simply granulated, it will absorb moisture quickly and react with carbon dioxide in the air. Calcium carbonate is formed by the granules, which causes them to clump easily. Even if they do not clump, the surface of the grains is difficult to dissolve, so even if you spray it on the soil, it will not disintegrate easily, making it ineffective. A product in which bentonite and vegetable mucilage were added to slaked lime was proposed as granular slaked lime that prevented granulation from caking and maintained high disintegration (Japanese Patent Application Laid-open No. 58-194738). What is vegetable mucilage? It refers to various natural gums, and their etherified derivatives are also said to be useful.However, it is difficult to expect a cheap and stable supply of imported natural products, and they are also disadvantageous in that they do not themselves contribute to alkalinity. Since it is a benefit, we would like to obtain the same effect without using such materials. [Problems to be solved by the invention] The purpose of the present invention is to obtain the same effect without using such materials. The object of the present invention is to provide granular slaked lime that has both long-term storage without solidification and rapid disintegration in water or soil, and a method for producing the same. The granular slaked lime of the present invention consists of an intimate mixture of 78-97% by weight of slaked lime and 3-22% by weight of colloidal hydrated aluminum silicate with a swelling degree of 8 Inl/2 g or more. 2 in 100 °C of distilled water
So-called A and C, in which a sample of g is dropped in about 20 times and the apparent capacity is read after 24 hours. This is a value measured using the C9 method. Typical colloidal hydrated aluminum silicate are:
It is montmorillonite or Na-type bentonite whose main component is montmorillonite. The method for producing the above granular slaked lime includes slaked lime 78-97
Colloidal hydrous aluminum silicate having a weight percent and swelling degree of 8 d/2 tj or more, typically the above-mentioned montmorillonite or Na-type bentonite containing it as a main component 3 to 22
% by weight, pressed to form, for example, a plate-shaped body, and then crushed and classified. It is preferable that montmorillonite or Na-type bentonite be as fine a powder as possible. Moreover, it is even more effective to use it by heating it to a temperature of 100 to 200° C. and drying it before use, and this is a recommended mode. [Function] The above-mentioned prior art document states that the combined use of vegetable mucilage and bentonite is essential, and that slaked lime granulated using bentonite alone has low disintegration. However, as a result of the research conducted by the present inventors, by using colloidal hydrous aluminum silicate such as montmorillonite or Na-type bentonite, which has a specific high swelling property, high disintegration and preservability can be achieved even without an organic binder. It was discovered that slaked lime with the following properties could be granulated. The fine powder of colloidal hydrated aluminum silicate, when mixed with the powder of slaked lime, coats its surface and - is present to separate each powder particle. As a result, moisture and charcoal gas in the environment come into contact with the slaked lime powder and are absorbed.
It acts as a hindrance to a reaction. High swelling ability means strong hygroscopicity or water absorption. When slaked lime absorbs water from the environment, colloidal hydrated aluminum silicate takes away the water, and the slaked lime's moisture absorption progresses. do not have. Combined with these effects, slaked lime hardly absorbs moisture during storage, prevents reaction with carbon dioxide gas, and suppresses particle caking and surface solidification of individual particles. On the other hand, when the granular slaked lime stored in this way is sprinkled on soil, the colloidal hydrated aluminum silicate intensely absorbs water in the soil and swells, expanding its volume. Fall apart. In other words,
collapses easily. In order to expect the above effects, the swelling degree of colloidal hydrous aluminum silicate such as montmorillonite or Na-type bentonite whose main component is montmorillonite must be 8 m/min.
Must be 2SF or more. Furthermore, if the amount of slaked lime mixed is less than 3% by weight, there will be no effect and high disintegration properties will not be obtained. Even if a large amount is added, the effect will be saturated, and if the amount is too large, the content of Ca(OH)2 will decrease, so the upper limit was set at 22%.

【実施例】【Example】

比較のため、消石灰だけをコンパティングマシンで圧縮
(圧力500Kgf/Cl1)して板状にし、解砕、分
級して粒状消石灰を得た。(Nα1)膨潤度16d/2
gのNa型ベントナイトを、そのまま(Nα2〜5)ま
たは150℃に1hr加熱して乾燥させてから(Nα6
〜9)、消石灰にそれぞれ3%、5%、10%または2
0%加えてミキサーで混合し、Nα1と同様にして粒状
消石灰を製造した。 これらをポリ袋に入れて放置し、製造直後、30日後お
よび45日後のサンプルを、東京肥糧検査所の定めた「
造粒した肥料の崩壊性試験法」に従って試験し、水中崩
壊残留率を測定した。 表に示した結果から明らかなように、本発明に従って製
造した粒状消石灰は、いずれも崩壊性がよい。 とくに
、乾燥させたNa型ベントナイトの使用は、非常に効果
的である。 発明の効果 本発明に従う粒状消石灰は、保存性および崩壊性にすぐ
れている。 これにより、取扱いの容易な肥料、土壌改
良剤、水改質材などを提供することができる。 特許出願人   吉沢石灰工業株式会社代理人  弁理
士  須 賀 総 夫 手続ネ市正書(自発) 昭和62年6月128 1、事件の表示 昭和62年特許願第1’16334号 2、発明の名称 粒状消石灰とその製造方法 3、補正をする者 事件との関係  特許出願人 住 所  東京都中央区銀座三丁目9番4号名 称  
吉澤石灰工業株式会社 代表者 吉澤兵左 4、代理人〒104 住 所  東京都中央区築地二丁目15番14号明細言
の発明の詳細な説明の欄 6、補正の内容
For comparison, only slaked lime was compressed using a compacting machine (pressure: 500 Kgf/Cl1) into a plate shape, crushed and classified to obtain granular slaked lime. (Nα1) Swelling degree 16d/2
g of Na-type bentonite as it is (Nα2-5) or heated to 150°C for 1 hr and dried (Nα6).
~9), slaked lime with 3%, 5%, 10% or 2
Granular slaked lime was produced in the same manner as Nα1 by adding 0% and mixing with a mixer. These were placed in a plastic bag and left to stand, and samples immediately after production, 30 days later, and 45 days later were collected according to the standards set by the Tokyo Fertilizer Inspection Center.
A test was conducted according to the "Disintegration Test Method for Granulated Fertilizer" to measure the residual rate of disintegration in water. As is clear from the results shown in the table, all of the granular slaked lime produced according to the present invention have good disintegration properties. In particular, the use of dried Na-type bentonite is very effective. Effects of the Invention The granular slaked lime according to the present invention has excellent preservability and disintegration properties. This makes it possible to provide fertilizers, soil conditioners, water modifying materials, etc. that are easy to handle. Patent Applicant: Yoshizawa Lime Industry Co., Ltd. Agent, Patent Attorney: Souo Suga Procedural Official Report (Spontaneous) June 1988 128 1. Indication of the Case 1988 Patent Application No. 1'16334 2. Name of the Invention Granular slaked lime and its manufacturing method 3, and its relationship to the amended case Patent applicant address: 3-9-4 Ginza, Chuo-ku, Tokyo Name:
Yoshizawa Lime Industry Co., Ltd. Representative: Hei Yoshizawa, left 4, Agent: 104 Address: 2-15-14 Tsukiji, Chuo-ku, Tokyo Column 6 of the detailed description of the invention in the specification, Contents of the amendment

Claims (4)

【特許請求の範囲】[Claims] (1)消石灰78〜97重量%と膨潤度8ml/2g以
上のコロイド性含水ケイ酸アルミニウムとの緊密な混合
物からなる粒状消石灰。
(1) Granular slaked lime consisting of an intimate mixture of 78-97% by weight of slaked lime and colloidal hydrated aluminum silicate with a swelling degree of 8 ml/2 g or more.
(2)コロイド性含水ケイ酸アルミニウムが、モンモリ
ロナイトまたはそれを主成分とするNa型ベントナイト
である特許請求の範囲第1項の粒状消石灰。
(2) The granular slaked lime according to claim 1, wherein the colloidal hydrated aluminum silicate is montmorillonite or Na-type bentonite containing montmorillonite as a main component.
(3)消石灰78〜97重量%と膨潤度8ml/2g以
上のコロイド性含水ケイ酸アルミニウム3〜22重量%
とを混合し、プレスして固化させた後、解砕し分級する
ことからなる粒状消石灰の製造方法。
(3) 78-97% by weight of slaked lime and 3-22% by weight of colloidal hydrated aluminum silicate with a swelling degree of 8ml/2g or more
A method for producing granular slaked lime, which comprises mixing, pressing and solidifying, and then crushing and classifying.
(4)コロイド性含水ケイ酸アルミニウムを、あらかじ
め100〜200℃の温度に加熱することにより乾燥さ
せて使用する特許請求の範囲第3項の粒状消石灰の製造
方法。
(4) The method for producing granular slaked lime according to claim 3, wherein colloidal hydrated aluminum silicate is dried by heating it in advance to a temperature of 100 to 200°C.
JP11633487A 1987-05-13 1987-05-13 Granular calcium hydroxide and manufacture thereof Granted JPS63282116A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11633487A JPS63282116A (en) 1987-05-13 1987-05-13 Granular calcium hydroxide and manufacture thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11633487A JPS63282116A (en) 1987-05-13 1987-05-13 Granular calcium hydroxide and manufacture thereof

Publications (2)

Publication Number Publication Date
JPS63282116A true JPS63282116A (en) 1988-11-18
JPH054339B2 JPH054339B2 (en) 1993-01-19

Family

ID=14684383

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11633487A Granted JPS63282116A (en) 1987-05-13 1987-05-13 Granular calcium hydroxide and manufacture thereof

Country Status (1)

Country Link
JP (1) JPS63282116A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6436891B1 (en) 1999-02-19 2002-08-20 Mionix Corporation Adduct having an acidic solution of sparingly-soluble group IIA complexes
US7323436B2 (en) * 1999-02-19 2008-01-29 Mionix Corporation Adduct having an acidic solution of sparingly-soluble group IIA complexes

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4932503B2 (en) * 2006-02-13 2012-05-16 ジェイカムアグリ株式会社 Disintegrating granular phosphate medium

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569689A (en) * 1978-11-18 1980-05-26 Shozo Aso Soil neutralizer

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569689A (en) * 1978-11-18 1980-05-26 Shozo Aso Soil neutralizer

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6436891B1 (en) 1999-02-19 2002-08-20 Mionix Corporation Adduct having an acidic solution of sparingly-soluble group IIA complexes
US7323436B2 (en) * 1999-02-19 2008-01-29 Mionix Corporation Adduct having an acidic solution of sparingly-soluble group IIA complexes

Also Published As

Publication number Publication date
JPH054339B2 (en) 1993-01-19

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