JPS5916503B2 - preferential flotation method - Google Patents

preferential flotation method

Info

Publication number
JPS5916503B2
JPS5916503B2 JP4882480A JP4882480A JPS5916503B2 JP S5916503 B2 JPS5916503 B2 JP S5916503B2 JP 4882480 A JP4882480 A JP 4882480A JP 4882480 A JP4882480 A JP 4882480A JP S5916503 B2 JPS5916503 B2 JP S5916503B2
Authority
JP
Japan
Prior art keywords
minerals
flotation
lead
copper
added
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
JP4882480A
Other languages
Japanese (ja)
Other versions
JPS56144757A (en
Inventor
隆造 武田
千秋 泉川
昌司 橋本
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 JP4882480A priority Critical patent/JPS5916503B2/en
Publication of JPS56144757A publication Critical patent/JPS56144757A/en
Publication of JPS5916503B2 publication Critical patent/JPS5916503B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は銅、鉛、亜鉛、鉄等の硫化鉱物を含む複雑硫化
鉱等からいわゆる亜硫酸浮選により各精鉱を得る優先浮
選法において、亜鉛鉱物と硫化鉄鉱物を抑制しながら銅
鉱物及び鉛鉱物を浮遊させて鉛鉱物又は銅・鉛バルク精
鉱を回収する方法の改良に関する。
Detailed Description of the Invention The present invention provides a preferential flotation method for obtaining various concentrates by so-called sulfite flotation from complex sulfide ores containing sulfide minerals such as copper, lead, zinc, and iron. The present invention relates to an improvement in a method for recovering lead minerals or copper/lead bulk concentrate by suspending copper minerals and lead minerals while suppressing.

従来、上記の方法において亜鉛鉱物と硫化鉄鉱物を充分
抑制するには、条件剤としてSO□又は亜硫酸塩を数k
g/lのオーダーで多量に添加しなければならず、その
場合鉛鉱物の浮遊性が極めて低下するので、銅・鉛鉱物
と亜鉛・硫化鉄鉱物との分離性を良好ならしめることは
難かしく、またSO□又は亜硫酸塩の添加が少な過ぎる
と銅鉱物の浮遊性が悪くなり、しかも亜鉛鉱物と硫化鉄
鉱物に対する抑制が不充分となる。
Conventionally, in order to sufficiently suppress zinc minerals and iron sulfide minerals in the above method, several kilograms of SO□ or sulfite were added as a conditioning agent.
It must be added in large amounts on the order of g/l, and in that case, the floatability of lead minerals is extremely reduced, making it difficult to achieve good separation between copper/lead minerals and zinc/iron sulfide minerals. Also, if the addition of SO□ or sulfite is too small, the buoyancy of copper minerals will be poor, and furthermore, zinc minerals and iron sulfide minerals will be insufficiently suppressed.

さらに、SO2又は亜硫酸塩の添加によって浮遊性の低
下した鉛鉱物を充分浮遊させるために捕収剤を多量に使
用すると、亜鉛鉱物と硫化鉄鉱物が浮遊し易くなって分
離性が悪化し、一方捕収剤が少な過ぎると亜鉛鉱物と硫
化鉄鉱物は充分抑制されるが鉛実収率が低下する等いず
れの場合も問題が多い。
Furthermore, if a large amount of scavenger is used to sufficiently suspend lead minerals whose buoyancy has decreased due to the addition of SO2 or sulfite, zinc minerals and iron sulfide minerals become easier to float, resulting in poor separation. If the amount of scavenger is too small, zinc minerals and iron sulfide minerals are sufficiently suppressed, but there are many problems in either case, such as a decrease in the actual lead yield.

本発明は亜鉛鉱物と硫化鉄鉱物を抑制するr、=め添加
したS02又は亜硫酸塩によって鉛鉱物の浮遊性が劣化
する問題点を解決し、浮選成績を向上させかつ操業コス
トの低廉化を図る目的で開発されたものである。
The present invention solves the problem of deterioration of floatability of lead minerals due to S02 or sulfite added to suppress zinc minerals and iron sulfide minerals, and improves flotation performance and reduces operating costs. It was developed for the purpose of

即ち、本発明は特に鉄液に空気混和を行ないながら条件
剤のSO□又は亜硫酸塩を添加することを特徴とするも
ので、その後捕収剤・起泡剤等の浮選試薬を用いて鉛優
先浮選又は銅・鉛バルク浮選を行なうのである。
That is, the present invention is characterized in that the conditioning agent SO□ or sulfite is added to the iron solution while aeration is performed, and then lead is removed using a flotation reagent such as a collection agent or a foaming agent. Priority flotation or copper/lead bulk flotation is carried out.

空気混和は専用のエアレータ−又は浮選機、エアリフト
等により行なうが、できるだけ微細気泡が発生するもの
がよい。
Aeration is carried out using a special aerator, flotation machine, air lift, etc., but it is preferable to use one that generates as fine air bubbles as possible.

また鉄液の酸性域でのpH調整は空気混和前から浮選試
薬添加前までの間に行なえばよい。
Further, the pH adjustment of the iron solution in the acidic range may be carried out between before mixing with air and before adding the flotation reagent.

空気混和の最適時間は対象鉱石や条件剤(S02又は亜
硫酸塩)の添加量によって異なり、鉛鉱物の浮遊性は最
適時間に達するまで時間と共に増大し、硫化鉄鉱物の浮
遊性は時間と共に低下して行く。
The optimum time for aeration differs depending on the target ore and the amount of conditioning agent (S02 or sulfite) added; the floatability of lead minerals increases with time until the optimum time is reached, and the floatability of iron sulfide minerals decreases with time. Go.

しかしながら、空気混和時間が最適時間を超えて長くな
ると、銅鉱物及び鉛鉱物の浮遊性は逆に悪くなって行く
However, when the aeration time becomes longer than the optimum time, the buoyancy of copper minerals and lead minerals becomes worse.

□SO2又は亜硫酸塩の添加は空気混和槽が2台以上あ
るときには最初の槽に添加した方が効果的である。
□When there are two or more aeration tanks, it is more effective to add SO2 or sulfite to the first tank.

また、空気混和とS02又は亜硫酸塩の添加は浮選試薬
(捕収剤等)の添加前に行なうことが必要で、浮選試薬
添加後ではその効果はない。
Furthermore, aeration and addition of S02 or sulfite must be performed before adding the flotation reagent (collection agent, etc.), and there is no effect after addition of the flotation reagent.

実施例 I A鉱山産の鉱石について従来法と本発明法を適用した場
合の回分式銅・鉛バルク浮選の結果を第1表と第2表に
示す。
Example I Tables 1 and 2 show the results of batch copper/lead bulk flotation when applying the conventional method and the method of the present invention to ore from Mine A.

A鉱山の鉱石は有用鉱物として黄銅鉱、方鉛鉱、閃亜鉛
鉱、黄鉄鉱、パライト及び少量の二次銅鉱物を含有して
いる。
The ore from Mine A contains chalcopyrite, galena, sphalerite, pyrite, pallite, and a small amount of secondary copper minerals as useful minerals.

A鉱山の鉱石を浮選粒度に粉砕した後、502(SO□
を水に溶かしてS02水としたもの。
After crushing ore from mine A to a flotation particle size, 502 (SO□
is dissolved in water to make S02 water.

以下同じ。same as below.

)3kg/lを添加して5分間条件付けを行ない、石灰
でpH5,9に調整後捕収剤としてエチルザンセート3
0.9/lと起泡剤としてダウフロス#250(商品名
)20.!li’/lを添加して行なった従来法による
回分式浮選の結果を第1表に示※す。
) 3 kg/l, conditioned for 5 minutes, adjusted the pH to 5.9 with lime, and added ethyl xanthate 3 as a scavenger.
0.9/l and Dowfloss #250 (trade name) as a foaming agent 20. ! Table 1 shows the results of batch flotation using the conventional method with the addition of li'/l.

また、第2表は本発明法を適用した場合の結果を示した
もので、鉄液に空気混和を行ないながらSO□を3k1
9/を最初の2分間で添加し、空気混和はSO2添加後
も続けて計20分間行ない、pH調整は空気混和の最後
の5分間で行ない石灰でpH5,9とし、空気混和終了
後エチルザンセート30,9/l、ダウフロス#250
を20 g / を添加して行なったものである。
In addition, Table 2 shows the results when the method of the present invention is applied.
9/ was added in the first 2 minutes, and aeration was continued for a total of 20 minutes after SO2 was added. The pH was adjusted during the last 5 minutes of aeration, and the pH was adjusted to 5.9 with lime. After the aeration was completed, ethylsanate was added. Sate 30.9/l, Dow Floss #250
The test was carried out by adding 20 g/.

第1表と第2表から従来法と本発明法を比較すると、各
鉱物の浮遊率はそれぞれ銅鉱物が76.9→83.4係
と向上し、鉛鉱物は44.9→84.4%と著しく向上
し、亜鉛鉱物は23.5→20.8係と抑制され、硫化
鉄鉱物は26.9→9.5係と非常によく抑制されてお
り、浮選成績が大幅に向上していることが判る。
Comparing the conventional method and the method of the present invention from Tables 1 and 2, the flotation rate of each mineral improved from 76.9 to 83.4 for copper minerals, and from 44.9 to 84.4 for lead minerals. %, zinc minerals were suppressed from 23.5 to 20.8, iron sulfide minerals were suppressed from 26.9 to 9.5, and the flotation results were significantly improved. It can be seen that

実施例 2 実施例1における本発明法において、S02添加量を1
kg/ tに減少させ、空気混和時間を15分と短く
した場合の浮選結果を第3表に示す。
Example 2 In the method of the present invention in Example 1, the amount of S02 added was reduced to 1
Table 3 shows the flotation results when the amount was reduced to 1 kg/t and the aeration time was shortened to 15 minutes.

第3表から判るように、銅及び鉛はよく浮遊しており、
S02添加量を少なくしたにもかかわらず亜鉛及び硫化
鉄はよく抑制されている。
As can be seen from Table 3, copper and lead are often suspended;
Zinc and iron sulfide are well suppressed despite the reduced amount of S02 added.

実施例 3 実施例1における本発明法において、さらに浮選時の捕
収剤としてKL#203 (ジイソプロピルジチオリン
酸ソーダの商品名)を80g/を添加した場合の浮選結
果を第4表に示す。
Example 3 Table 4 shows the flotation results when 80 g of KL #203 (trade name of sodium diisopropyldithiophosphate) was added as a collecting agent during flotation in the method of the present invention in Example 1. .

; 第4表から判るように、浮選開始後約6分で各鉱物
の浮遊率は銅鉱物83.5%、鉛鉱物9o、9%と高く
、亜鉛鉱物21.0%、硫化鉄鉱物7.9%と非常に良
好な分離成績が得られた。
As can be seen from Table 4, approximately 6 minutes after the start of flotation, the flotation rate of each mineral was as high as 83.5% for copper minerals, 9% for lead minerals, 21.0% for zinc minerals, and 7% for iron sulfide minerals. A very good separation result of .9% was obtained.

以上のように、本発明法によれば各種硫化鉱物を含有す
る鉱石の鉛浮選又は銅・鉛バルク浮選に適用することに
より、鉛鉱物の浮遊性が著しく向上すると共に銅鉱物も
よく浮遊し、一方亜鉛鉱物と硫化鉄鉱物は選択的によく
抑制されるので浮選成績が向上し、添加する捕収剤等の
量も少なくて済むのでランニングコストの低廉化を図る
ことができる。
As described above, when the method of the present invention is applied to lead flotation of ores containing various sulfide minerals or copper/lead bulk flotation, the flotation of lead minerals is significantly improved, and copper minerals are also easily floated. On the other hand, zinc minerals and iron sulfide minerals are selectively and well suppressed, so the flotation results are improved, and the amount of added scavenger etc. can be reduced, so running costs can be reduced.

さらに、本発明では鉛鉱物が浮選初期からよく浮遊して
分離性が非常に高いので鉛浮選を行なう場合に従来より
も小規模の浮選機で済み、また銅・鉛バルク浮選を行な
う場合にも前述のように少量の捕収剤で良好な結果が得
られるからその後工程の銅・鉛分離浮選における両者の
分離性も一層向上させることができる等種々の利点を有
する。
Furthermore, in the present invention, lead minerals float well from the initial stage of flotation and have very high separability. Even in this case, as mentioned above, good results can be obtained with a small amount of collector, so that the separability of copper and lead in the subsequent step of separation and flotation can be further improved, and has various advantages.

Claims (1)

【特許請求の範囲】[Claims] 1 銅、鉛、亜鉛、鉄等の硫化鉱物を含む鉱石から鉛浮
選又は銅・鉛バルク浮選を行なうに際して、鉄液に空気
混和を行ないながら条件剤としてのS02又は亜硫酸塩
を添加することを特徴とする優先浮選法。
1. When carrying out lead flotation or copper/lead bulk flotation from ores containing sulfide minerals such as copper, lead, zinc, iron, etc., adding S02 or sulfite as a conditioning agent while aerating the iron solution. A preferential flotation method characterized by
JP4882480A 1980-04-14 1980-04-14 preferential flotation method Expired JPS5916503B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4882480A JPS5916503B2 (en) 1980-04-14 1980-04-14 preferential flotation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4882480A JPS5916503B2 (en) 1980-04-14 1980-04-14 preferential flotation method

Publications (2)

Publication Number Publication Date
JPS56144757A JPS56144757A (en) 1981-11-11
JPS5916503B2 true JPS5916503B2 (en) 1984-04-16

Family

ID=12813966

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4882480A Expired JPS5916503B2 (en) 1980-04-14 1980-04-14 preferential flotation method

Country Status (1)

Country Link
JP (1) JPS5916503B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0137523Y2 (en) * 1984-11-09 1989-11-13

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4238244C2 (en) * 1992-11-12 1994-09-08 Metallgesellschaft Ag Process for the selective flotation of a sulfidic copper-lead-zinc ore
PE20130503A1 (en) * 2009-12-04 2013-04-22 Barrick Gold Corp SEPARATION OF COPPER MINERALS FROM PYRITE USING AN AIR-METABISULPHITE TREATMENT
CN103008112A (en) * 2012-11-30 2013-04-03 广西高峰矿业有限责任公司 Selective milling-flotation method for cassiterite multi-metal sulfide ore

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0137523Y2 (en) * 1984-11-09 1989-11-13

Also Published As

Publication number Publication date
JPS56144757A (en) 1981-11-11

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