JPS5939387A - Neutralizing agent - Google Patents

Neutralizing agent

Info

Publication number
JPS5939387A
JPS5939387A JP14754782A JP14754782A JPS5939387A JP S5939387 A JPS5939387 A JP S5939387A JP 14754782 A JP14754782 A JP 14754782A JP 14754782 A JP14754782 A JP 14754782A JP S5939387 A JPS5939387 A JP S5939387A
Authority
JP
Japan
Prior art keywords
neutralizing agent
neutralizing
sulfuric acid
neutralization
salt
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.)
Pending
Application number
JP14754782A
Other languages
Japanese (ja)
Inventor
Yoneji Nishida
西田 米治
Yoshiya Itou
伊藤 義弥
Hiroyuki Harada
寛之 原田
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.)
Dowa Holdings Co Ltd
Original Assignee
Dowa Mining 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 Dowa Mining Co Ltd filed Critical Dowa Mining Co Ltd
Priority to JP14754782A priority Critical patent/JPS5939387A/en
Publication of JPS5939387A publication Critical patent/JPS5939387A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the titled neutralizing agent having the excellent efficiency of neutralization without the need of mechanical agitation, by forming a mixture comprising a calcium neutralizing agent and a salt composed of an atom or an atomic group other than Ca or SO4. CONSTITUTION:The mixture comprising a Ca neutralizing agent (e.g. slaked lime or calcium carbonate) and a salt (e.g. NaCl) composed of an atom or an atomic group other than Ca or SO4 is formed in the presence or absence of a binder (e.g. cement) to obtain the neutralizing agent. This neutralizing agent is esp. suitable for neutralizing sulfuric acid water flowing out of an unmanned unworked or abolished mine, etc. difficult to receive an electric power source. By the presence of said neutralizing agent in the outflow sulfuric acid water, neutralization can be unmannedly realized with high efficiency for over a long time without the need to use driving power, even if mechanical agitation is not completely performed. Thus, the prevention of environmental pollution can be effectively realized while saving installation, labor and driving power.

Description

【発明の詳細な説明】 本発明は、特に硫酸酸性水を中和処理するのに適した中
和用材料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a neutralizing material particularly suitable for neutralizing sulfuric acid water.

従来、硫[fl性水に消石灰、炭酸カルシウム、苛性ソ
ーダ、水酸化アンモニウム等の中和剤を使用して中和処
理されているが、処理量が多い鉱山排水などの場合vc
ll−r安価な消石灰、炭酸カルシウム等のカルシウム
系中和剤が使用されることカニ多い。しかし、硫酸酸性
水に対してカルシウム系中和剤金使用する場合kにその
中和処理にいくつかの問題があった。これに中和反応l
F−よって生fy、すれるCa5O4Vc基因てる場合
が多い。すなわちCaSO4の水に対する溶解度は小ざ
いので中和剤の表面に0aSO4の薄層が形成され、こ
れが中和反応ケ阻害する。この析出[また0aSO4に
よって中オロ反応速度が低下し、中和剤の効率も低下す
るので、中和設備も大型化せざるを得す、中和剤の使用
Itも多くならざるを得ない。このπめ前記0aSO4
薄層全除去して中和反応を効率的に行うべく液全体全機
械攪拌することが通常行なわれるが、この場合!cid
設備費・動力費が嵩むほか、無人の体廃止鉱山等におい
て硫酸酸性水が少量ずつ発生する工うな場合等は、機械
攪拌することも実質上不可能であり、この工う1機械攪
拌を璧しない経済的な中11処理法が強く望まれてい罠
Conventionally, sulfur [fl] water is neutralized using neutralizing agents such as slaked lime, calcium carbonate, caustic soda, and ammonium hydroxide, but in the case of mine drainage where a large amount of water is to be treated, VC
Inexpensive calcium-based neutralizing agents such as slaked lime and calcium carbonate are often used. However, when using calcium-based neutralizing agent gold for sulfuric acid acid water, there were some problems in the neutralization process. This is followed by a neutralization reaction.
F- is often caused by a Ca5O4Vc base. That is, since the solubility of CaSO4 in water is low, a thin layer of 0aSO4 is formed on the surface of the neutralizing agent, which inhibits the neutralization reaction. This precipitation [0aSO4 also lowers the neutralization reaction rate and reduces the efficiency of the neutralizing agent, so the size of the neutralization equipment must be increased and the amount of neutralizing agent used must also increase. This π above 0aSO4
Normally, the entire liquid is mechanically stirred in order to completely remove the thin layer and carry out the neutralization reaction efficiently, but in this case! cid
In addition to increasing equipment and power costs, mechanical agitation is virtually impossible in cases such as unmanned decommissioned mines where sulfuric acid acid water is generated little by little. There is a strong need for an economical treatment method that does not cause such problems.

本発明はこのような要求?aた丁中オロ効率のよい中和
剤の提供全目的としたもので、この目的において種々の
試験研究を重ねた結果、カル7ウム系中和剤に、Ca 
iたはSO4以外の原子またに原子団;2)>う;’z
る塩類を混合し、これをバインダーの存在下または非存
在下で塊状に゛成形した新規な中和用材料を開発するこ
とができた。ここで、カル/ラム系中和剤とげ、消石灰
や炭酸カルシウム等の通常の中和剤であり、(aまたげ
SO4以外の原子種たは原子団刀・らなる塩類は、Na
2003. Mgct2゜リグニ/スルホン酸塩、Na
ct等などを意味するが、代表例として1″tNact
i挙げることができる。
Does the present invention meet such requirements? The overall purpose was to provide a highly efficient neutralizing agent, and as a result of various tests and studies for this purpose, we found that calcium-based neutralizing agents
i or atoms or atomic groups other than SO4;2)>u;'z
We were able to develop a new neutralizing material by mixing salts and forming them into a lump in the presence or absence of a binder. Here, the Cal/Rum neutralizer is a normal neutralizing agent such as thorn, slaked lime, and calcium carbonate.
2003. Mgct2゜Ligni/Sulfonate, Na
ct, etc., but a typical example is 1″tNact.
i can list.

塊状に成形するVcに、混合物を圧縮成形その他の方法
により、適当な大きさの塊状としてもよいが、セメント
等のバインダーを用いて強度を高めることもできる。
The mixture may be formed into a block of an appropriate size by compression molding or other methods, but the strength can also be increased by using a binder such as cement.

本発明による中和用材料(中和ボールンを用いて硫酸酸
性水を中和すると、後記実施例に示すように、カルシウ
ム系中和剤単独で中和処理する場合vr−fヒして、機
械攪拌を行なわなくとも著しく中和効率が良好となる。
When sulfuric acid acid water is neutralized using the neutralizing material (neutralizing ball) according to the present invention, as shown in the examples below, when neutralizing with a calcium-based neutralizing agent alone, vr-f Even without stirring, the neutralization efficiency is significantly improved.

これは、本発明の中和材料中のCa、SO4以外の原子
またげ原子団からなる塩類が、この塊状材料表面に対す
るCaSO4の析出全阻止する作用を供するからである
と考えられる。
This is thought to be because the salts consisting of atomic groups spanning atoms other than Ca and SO4 in the neutralized material of the present invention serve to completely inhibit the precipitation of CaSO4 on the surface of the bulk material.

このような効果に、セメ/トラ使用して本発明の中和材
料全結合したとしても十分に現われ、機゛械的攪拌を行
なわずとも塊状中和材料の表面部のみならず中心部まで
効率よく反応させることができる。
This effect is fully manifested even when the neutralized material of the present invention is completely combined using a cement/torer, and even without mechanical stirring, it is possible to efficiently combine not only the surface of the bulk neutralized material but also the center. It can react well.

従って、本発明の中和材料は、電源の入手が困難で無人
の体廃止鉱山等から流出する硫酸酸性水の中和処理など
に特に適しており、この流出する硫酸酸−性中に本発明
の中和材料を存在させておけば、機械攪拌を全く行なわ
なくとも、中和処理全効率よく行なうことが可能で、無
人、無動力、長期間の中和処理が実現でき、公害防止ケ
、省設備、省労力、省動力的に、かつ効果的に実施でき
る。
Therefore, the neutralizing material of the present invention is particularly suitable for neutralizing sulfuric acid water that flows out from unmanned abandoned mines where it is difficult to obtain a power source. If a neutralizing material is present, it is possible to carry out the neutralization process efficiently without any mechanical agitation, and it is possible to realize unattended, non-powered, long-term neutralization process, and to prevent pollution. It can be implemented effectively with less equipment, less labor, and less power.

実施例 1 pH4,0の硫酸酸性水41に対して、消石灰277と
セメント67とから成る塊状中和剤1個で中和した場合
と、消石灰277とセメント6りと食塩202とから成
る塊状中和剤1個で中和した場合の夫々の経過時間とp
Hの関係音調べた。その結果を第1図に示した。この結
果から食塩の含有される塊状中和剤の方が中和速度が著
しくはやいことがわかる。
Example 1 A case in which sulfuric acid acidic water 41 with a pH of 4.0 was neutralized with one block neutralizer consisting of slaked lime 277 and cement 67, and a block neutralizer consisting of slaked lime 277, cement 6 and table salt 202. Elapsed time and p when neutralized with one Japanese additive
I looked up the sounds related to H. The results are shown in Figure 1. This result shows that the neutralization rate of the bulk neutralizer containing salt is significantly faster.

!、1ζ、pH3,7の硫酸酸性水4tVC対して、消
石灰272とセメント62とから成る塊状中和剤2個で
中和した場合と、消石灰271とセメント59と食塩2
07と刀1ら成る塊状中和剤2個で中和した場合の夫々
の経過時間とpHの関係は第2図に示す通りとなった。
! , 1ζ, 4 tVC of sulfuric acid acid water with pH 3.7, neutralized with two bulk neutralizers consisting of slaked lime 272 and cement 62, and slaked lime 271, cement 59 and common salt 2
The relationship between the elapsed time and pH when neutralizing with two bulk neutralizers consisting of 07 and Katana 1 was as shown in FIG. 2.

やぽり食塩の含有される塊状中和剤の方が中和速度が著
しくはやいことがわかる。
It can be seen that the neutralization rate of the block neutralizer containing Yapori salt is significantly faster.

実施例 2 次の第1表に示す構成の5種の塊状中和剤と、pH4,
0の硫酸酸性水を準備して中和試験を行った。
Example 2 Five types of bulk neutralizers having the compositions shown in Table 1 below, pH 4,
A neutralization test was conducted by preparing 0 sulfuric acid acid water.

第  1  表 (イ) pH4,0の硫酸酸性水41VC対して塊状中
和剤A2個で中和した場合の経過時間とpHの関係は第
6図(a)Vc示す通りである。a点、b点において夫
々の塊状中和剤に亀裂が入って破損しその付近でpHが
急激に上昇するものの、後述するB10、D、E[比較
し、著しく中和速度が遅く、塊状体としての固結度も悪
い。
Table 1 (a) The relationship between elapsed time and pH when 41 VC of sulfuric acid acidic water having a pH of 4.0 was neutralized with two pieces of bulk neutralizing agent A is as shown in FIG. 6 (a) Vc. At points a and b, each of the bulk neutralizers cracks and breaks, and the pH rises rapidly in the vicinity; The degree of consolidation is also poor.

(ロ)pH4,0の硫酸酸性水4tに対して塊状中和剤
82個で中和すると、第3図(b) Vc示すように、
50分でpH7,OVc達り、7m。中和水f pH4
,0ノ硫酸酸性水4tvc取替えると95分でpH7,
0Vc達した。再び中和水をpH4,0の硫酸酸性水4
tVC取替えると105分でpH7,0IC達した。食
塩全含有しない第6図(a)VC比較し、中和速度が著
しく向上しており、耐用時間も長い。
(b) When 4 tons of sulfuric acid acidic water with a pH of 4.0 is neutralized with 82 bulk neutralizers, as shown in Figure 3 (b) Vc,
pH 7, OVc reached in 50 minutes, 7m. Neutralized water f pH4
,0 Nosulfuric acid acidic water 4tvc replaced, pH 7 in 95 minutes,
It reached 0Vc. Add neutralized water again to sulfuric acid acid water with pH 4.0
When tVC was replaced, pH reached 7.0 IC in 105 minutes. Compared to the VC shown in Figure 6 (a) which does not contain any salt, the neutralization rate is significantly improved and the service life is longer.

(ハ)(ロ)と同様にして、各2個の塊状中和剤0.D
、EでpH4,0の硫酸酸性水4tを各4回中和した結
果全夫々第5図(C)、第3図(d)、第3図(e)v
c示した。食塩の添加緻ヲ増加すれば、A→B −+ 
Oと中和速度は大きくなる傾向があるが、C!、D、E
の間には大きな差異は認められなかった。
(c) In the same manner as in (b), two pieces of block neutralizer 0. D
The results of neutralizing 4 tons of sulfuric acid acidic water with a pH of 4.0 with E and E four times each are shown in Figures 5 (C), 3 (d), and 3 (e), respectively.
c showed. If the addition of salt increases, A→B −+
O and neutralization rate tend to increase, but C! ,D,E
No major differences were observed between them.

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

第1図げ従来の中和剤vc、1:るpHの経時変化図、
第2図a本発明の中和材料によるpHの経時変化図、第
3図a本発明の中和材の種類と量を変えた場合のpHの
経時変化図である。
Figure 1 is a graph of the pH change over time of the conventional neutralizing agent VC, 1:
FIG. 2a is a graph of pH change over time using the neutralizing material of the present invention, and FIG. 3a is a graph of pH change over time when the type and amount of the neutralizing material of the present invention are varied.

Claims (1)

【特許請求の範囲】 <11  カルシウム系中和剤と、CaまたH so4
以外の原子または原子団から構成される塩と、刀工らな
る混合物をバインダーの存在下または非存在下で成形し
てなる中和用材料。 (2)塩(dNact″′Cある特許請求の範囲第1項
記載の中和用材料。 (3)  バインダーはセメントである特許請求の範囲
第1項またに第2項記載の中和用材料。
[Claims] <11 Calcium-based neutralizer and Ca or H so4
A neutralizing material made by molding a mixture of a salt composed of atoms or atomic groups other than those of other atoms and a swordsmith in the presence or absence of a binder. (2) The neutralizing material according to claim 1, which is salt (dNact'''C). (3) The neutralizing material according to claim 1 or 2, wherein the binder is cement. .
JP14754782A 1982-08-27 1982-08-27 Neutralizing agent Pending JPS5939387A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14754782A JPS5939387A (en) 1982-08-27 1982-08-27 Neutralizing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14754782A JPS5939387A (en) 1982-08-27 1982-08-27 Neutralizing agent

Publications (1)

Publication Number Publication Date
JPS5939387A true JPS5939387A (en) 1984-03-03

Family

ID=15432784

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14754782A Pending JPS5939387A (en) 1982-08-27 1982-08-27 Neutralizing agent

Country Status (1)

Country Link
JP (1) JPS5939387A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5980391A (en) * 1982-10-30 1984-05-09 Dowa Mining Co Ltd Material for neutralization
KR100330334B1 (en) * 1999-05-10 2002-04-01 곽영훈 Method purifying acid waste water by using natural water
JP2020093222A (en) * 2018-12-13 2020-06-18 リンナイ株式会社 Method for manufacturing neutralizer comprising calcium carbonate molded body

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5980391A (en) * 1982-10-30 1984-05-09 Dowa Mining Co Ltd Material for neutralization
JPS634479B2 (en) * 1982-10-30 1988-01-29 Dowa Mining Co
KR100330334B1 (en) * 1999-05-10 2002-04-01 곽영훈 Method purifying acid waste water by using natural water
JP2020093222A (en) * 2018-12-13 2020-06-18 リンナイ株式会社 Method for manufacturing neutralizer comprising calcium carbonate molded body

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