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JPS61127833A - Recovery of mercury in iron sulfide concentrate - Google Patents

Recovery of mercury in iron sulfide concentrate

Info

Publication number
JPS61127833A
JPS61127833A JP59248756A JP24875684A JPS61127833A JP S61127833 A JPS61127833 A JP S61127833A JP 59248756 A JP59248756 A JP 59248756A JP 24875684 A JP24875684 A JP 24875684A JP S61127833 A JPS61127833 A JP S61127833A
Authority
JP
Japan
Prior art keywords
iron sulfide
silver
leaching
sulfide concentrate
recovery
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
JP59248756A
Other languages
Japanese (ja)
Inventor
賀川 鉄一
ジヤツク・マーフイー
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.)
Eneos Corp
Original Assignee
Nippon 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 Nippon Mining Co Ltd filed Critical Nippon Mining Co Ltd
Priority to JP59248756A priority Critical patent/JPS61127833A/en
Publication of JPS61127833A publication Critical patent/JPS61127833A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Manufacture And Refinement Of Metals (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】 発明の分野 本発明は、硫化鉄精鉱中に含まれる銀を回収する方法に
関するものであり、特には精鉱を燐鉱することなく背比
法以外の方法で銀を簡易効率的に回収する方法に関する
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for recovering silver contained in iron sulfide concentrate, and more particularly to a method for recovering silver contained in iron sulfide concentrate by a method other than the back ratio method without phosphatizing the concentrate. Concerning a simple and efficient method of collection.

発明の背景 銀の回収源の一つとして硫化鉄鉱がある。この精鉱であ
る硫化鉄精鉱から銀を回収する方法はこれまで専ら、硫
酸焼鉱に冶金的手段を適用する技術に依存していたが、
硫酸原料としての販路が狭められた結果、これ以外のル
ートで銀を回収する必要性が生じている。
BACKGROUND OF THE INVENTION One of the sources of silver recovery is iron sulfide. The method of recovering silver from this iron sulfide concentrate has so far relied exclusively on the application of metallurgical means to sulfuric acid burnt ore.
As a result of the narrowing of sales channels for sulfuric acid as a raw material, there is a need to recover silver through other routes.

鉱石中の金、銀を浸出する方法としては・薄いNaCN
溶液で浸出を行う背比法を用いるのがごく一般的である
が、鉱石中に硫黄が存在する場合に背比法を適用すると
液中に千オシアンイオン(−CNS)が生成して、浸出
剤の浪費と浸出率の低下をもたらすので、背比法を適用
する前に、比選、浮選あるいは焙焼などにより硫黄を除
去しておかねばならない。しかしながら、硫化鉄精鉱中
の銀が硫化鉄鉱物自体の中に分布しているので、比選や
浮選による脱硫法の適用は無意味であり、また焙焼すれ
ば廃ガスの処理に多額の経費を要する。現在では、背比
物の使用自体に周囲のフンセンサスが得られ難い状況に
ある。こうした理由のため、硫化鉄精鉱への背比法の適
用はもはや考えられないと云ってよい。
As a method for leaching gold and silver in ore, ・Thin NaCN
It is very common to use the back ratio method, which performs leaching with a solution, but if the back ratio method is applied when sulfur is present in the ore, 1,000 osyanide ions (-CNS) will be generated in the solution, which will cause leaching. Before applying the leaching method, sulfur must be removed by sifting, flotation, roasting, etc., as this results in waste of the agent and a decrease in the leaching rate. However, since the silver in iron sulfide concentrate is distributed within the iron sulfide mineral itself, it is meaningless to apply desulfurization methods such as selective selection or flotation, and roasting requires a large amount of waste gas treatment. costs. At present, it is difficult to gain public appreciation for the use of comparables. For these reasons, it can be said that the application of the back ratio method to iron sulfide concentrates is no longer considered.

従って、背比法に代る新たな硫化鉄精鉱からの銀回収法
の確立が要望されている。
Therefore, there is a demand for the establishment of a new method for recovering silver from iron sulfide concentrates in place of the Sebi method.

11!」すし そこで本発明者等は、背比法に代る浸出法により硫化鉄
精鉱からの銀の回収を図るべく、浸出剤及び処理プロセ
スについて検討を重ねた。銀鉱物は硫化鉄精鉱中に緻密
に存在している為通常の物理的方法で脱硫することは不
可能であり、他方焙暁により脱硫を行うことは経費面及
び廃ガス処理上の問題が生じ実施困難である。硫化鉄精
鉱をオートクレープにて強制酸化するのが、銀鉱物を黄
鉄鉱から分離するのに有効な手段であることが知見され
た。更に、こうしてオートクレープ処理された残渣に対
して浸出剤としてチオ尿素あるいはチオ硫酸ナトリウム
を用いるのが好適であることが判明した。これら段階を
組合せることにより、非常に効率的な銀浸出プロセスが
確立される。
11! Therefore, the present inventors conducted repeated studies on leaching agents and treatment processes in order to recover silver from iron sulfide concentrate by a leaching method instead of the back ratio method. Since silver minerals are densely present in iron sulfide concentrate, it is impossible to desulfurize them using normal physical methods.On the other hand, desulfurization by roasting poses problems in terms of cost and waste gas treatment. This is difficult to implement. It has been found that forced oxidation of iron sulfide concentrate in an autoclave is an effective means for separating silver minerals from pyrite. Furthermore, it has been found to be suitable to use thiourea or sodium thiosulfate as a leaching agent for the autoclaved residue in this way. By combining these steps a highly efficient silver leaching process is established.

斯くして、本発明は、硫化鉄精鉱をオートクレープ中で
強制的に酸化した後ろ過し、その残渣に対して浸出剤と
してチオ尿素あるいはチオ硫酸ナトリウムを用いて浸出
を行うことを特徴とする硫化鉄精鉱中の銀°を回収する
方法を提供する。
Thus, the present invention is characterized in that iron sulfide concentrate is forcibly oxidized in an autoclave, filtered, and the residue is leached using thiourea or sodium thiosulfate as a leaching agent. Provided is a method for recovering silver° in iron sulfide concentrate.

図は、本発明に従う方法の系統図である。硫化鉄精鉱は
その出所源に応じて様々の量の銀を含有しているが、成
る鉱山産の硫化鉄精鉱を例にとると、FIe:40〜5
0%、8:45〜50%、λgニア0〜150.9/)
ンの組成を有している。
The figure is a diagram of the method according to the invention. Iron sulfide concentrates contain varying amounts of silver depending on their source, but for example, iron sulfide concentrates from mines have a FIe of 40 to 5.
0%, 8:45-50%, λgnia 0-150.9/)
It has the composition of

こうした硫化鉄精鉱は、一般にD5゜(積算分布曲線の
50%に相当する粒子径で、この径以上と以下の粒子1
so%ずつ)=30〜50pmf)粒寸を有しているが
、これを例えばボールミル等により摩砿することによっ
て銀浸出率の向上を図ることができる。
These iron sulfide concentrates are generally D5° (particle size corresponding to 50% of the cumulative distribution curve, with particles larger than and smaller than 1
The grain size is 30 to 50 pmf), but the silver leaching rate can be improved by milling it with a ball mill or the like.

硫化鉄精鉱は、必要に応じ摩鉱後、オートクレープにお
いて酸化処理を受ける。オートクレープにおいて硫化鉄
精鉱は、攪拌を行いながら酸素及び水の存在下で長時間
酸化処理される。酸化条件は、使用するオートクレープ
設備、磁石の組成、処理量等によって変動する。硫黄の
融点(113°C)以下の温度、例えば常温〜90°C
において酸素分圧tO〜5.Oatmの下で実施できる
。充分な攪拌を行いつつ、70〜100時間の攪拌時間
が使用される。酸化処理により、硫化鉄精鉱の主体たる
黄鉄鉱は酸化・分解し、銀砿物は黄鉄鉱から分離する。
The iron sulfide concentrate is subjected to oxidation treatment in an autoclave after grinding if necessary. In the autoclave, the iron sulfide concentrate is oxidized for a long time in the presence of oxygen and water with stirring. Oxidation conditions vary depending on the autoclave equipment used, the composition of the magnet, the processing amount, etc. Temperature below the melting point of sulfur (113°C), e.g. room temperature to 90°C
At oxygen partial pressure tO~5. It can be implemented under Oatm. A stirring time of 70 to 100 hours is used with sufficient stirring. Through oxidation treatment, pyrite, which is the main component of iron sulfide concentrate, is oxidized and decomposed, and silverite is separated from pyrite.

硫黄の融点より高い温度でオートクレープ処理を行うと
、粒子アグロメレーションのため、オートクレープ操作
が難しくなる傾向があるので、上記のように処理温度を
選定することが好ましい。
If autoclaving is performed at a temperature higher than the melting point of sulfur, the autoclaving operation tends to become difficult due to particle agglomeration, so it is preferable to select the treatment temperature as described above.

ろ過後の残渣は、チオ尿素或いはチオ硫酸ナトリウムを
浸出剤として浸出を行うことによりチオ尿素ではほぼ1
00%そしてチオ硫酸ナトリウムでは80%の銀浸出率
を得ることができる。これは従来法と較べると格段に高
い値である。チオ尿素の方が高い銀浸出率を与えるが、
反面試薬費が高fifliでありまたpHを低く保つ必
要があるという不利な面もある。実操業においてどちら
の浸出剤を選択するかは、対象とする鉱石に応じての経
済性に基いて定められる。
By leaching the residue after filtration using thiourea or sodium thiosulfate as a leaching agent, thiourea is reduced to approximately 1%.
Silver leaching rates of 0.00% and 80% can be obtained with sodium thiosulfate. This is a much higher value than the conventional method. Although thiourea gives a higher silver leaching rate,
On the other hand, there are disadvantages in that the reagent cost is high and the pH must be kept low. Which leaching agent to select in actual operation is determined based on economic efficiency depending on the target ore.

浸出した銀は、電解法あるいはイオン交換法等の従来か
ら確立されている方法により容易に回収することが可能
である。
Leached silver can be easily recovered by conventionally established methods such as electrolytic method or ion exchange method.

実施例 ある鉱山産の硫化鉄精鉱(F@45%、850%、Ag
11 Qg/l−ンχを対象として、オートクレープ酸
化及び浸出処理を順次して実施した。
Example Iron sulfide concentrate (F@45%, 850%, Ag
Autoclave oxidation and leaching treatments were performed sequentially on 11 Qg/l-on χ.

各条件を第1表及び第2表に示す。Each condition is shown in Tables 1 and 2.

第1表 オートクレープ酸化条件 硫化鉄精@         45g 水                  45 〇−温
  度                80°C酸素
分圧         2.05 atm攪拌速度  
       450 rpm第2表 浸出条件および
浸出結果 第2表かられかるように、非常に高い銀浸出率が得られ
た。比較例にて示すように資化法による銀浸出率はせい
ぜい34%程度であり、その増加率は顕著である。
Table 1 Autoclave oxidation conditions Iron sulfide refinery @ 45g Water 45 - Temperature 80°C Oxygen partial pressure 2.05 atm Stirring speed
450 rpm Table 2 Leaching conditions and leaching results As can be seen from Table 2, a very high silver leaching rate was obtained. As shown in the comparative example, the silver leaching rate by the assimilation method is about 34% at most, and the rate of increase is remarkable.

実施例と同一の硫化鉄精鉱に対してNaCN5Jil/
l (pH:1α5)溶液で24時間攪拌した。
NaCN5Jil/ for the same iron sulfide concentrate as in the example.
1 (pH: 1α5) solution for 24 hours.

得られた銀浸出率は34%にすぎなかった。The silver leaching rate obtained was only 34%.

参考例 実施例1と同じ硫化鉄精鉱に対してオートクレープ酸化
処理を行わず、直接、チオ尿素浸出を行った。ボールミ
ルでΦ摩鉱の効果を見るため、上記硫化鉄精鉱をボール
ミルで摩鉱し、摩鉱時間を変えることにより下表に示す
様々の粒寸のものを:!4製した。これら様々の粒寸の
硫化鉄精鉱に対してo、5モy/lのチオ尿素溶液(硫
酸にてpH=tOに調整)を用いて9時Ivl浸出した
。結果を下表に示す。
Reference Example The same iron sulfide concentrate as in Example 1 was directly subjected to thiourea leaching without being subjected to autoclave oxidation treatment. In order to see the effect of Φ ore in a ball mill, the above iron sulfide concentrate was milled in a ball mill, and by changing the milling time, various grain sizes as shown in the table below were obtained:! 4 were made. These iron sulfide concentrates of various particle sizes were leached at 9:00 Ivl using a thiourea solution of 5 moy/l (adjusted to pH=tO with sulfuric acid). The results are shown in the table below.

0      4α0      54.415   
    29.2      34.750     
  19、4      37.1s45      
 14.6      4!i、660       
14.6      45.5銀浸出率は比較例で示し
た資化法の場合と同水準の34%程度しかない。これに
より、本発明においてオートクレープ酸化処理が銀浸出
率向上に重要な役割を果していることがわかる。摩鉱に
よる粒寸の減少は、銀浸出率に5〜10%の改善を与え
るものと思われる。
0 4α0 54.415
29.2 34.750
19, 4 37.1s45
14.6 4! i, 660
14.6 45.5 The silver leaching rate is only about 34%, which is the same level as the assimilation method shown in the comparative example. This shows that the autoclave oxidation treatment plays an important role in improving the silver leaching rate in the present invention. Grain size reduction by grinding appears to provide a 5-10% improvement in silver leaching rate.

発明の効果 資化法に代る銀回収法として資化法に較べて格段に高い
銀浸出率を与えしかも従来問題となった廃ガス対策等を
要しない効率的な硫化鉄精鉱からの銀回収法が確立され
たことの工業的意義はきわめて大きい。
Effects of the Invention As an alternative silver recovery method to the assimilation method, it is an efficient method for recovering silver from iron sulfide concentrate that provides a much higher silver leaching rate than the assimilation method and does not require the conventional problems of waste gas countermeasures. The industrial significance of establishing a recovery method is extremely large.

図面は本発明方法の流れ系統唄である。The drawing is a flow diagram of the method of the present invention.

r]をr]

Claims (1)

【特許請求の範囲】[Claims] 1)硫化鉄精鉱をオートクレープ中で強制的に酸化した
後ろ過し、その残渣に対して浸出剤としてチオ尿素ある
いはチオ硫酸ナトリウムを用いて浸出を行うことを特徴
とする硫化鉄精鉱中の銀を回収する方法。
1) An iron sulfide concentrate characterized by forcibly oxidizing the iron sulfide concentrate in an autoclave, filtering it, and leaching the residue using thiourea or sodium thiosulfate as a leaching agent. How to recover silver.
JP59248756A 1984-11-27 1984-11-27 Recovery of mercury in iron sulfide concentrate Pending JPS61127833A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59248756A JPS61127833A (en) 1984-11-27 1984-11-27 Recovery of mercury in iron sulfide concentrate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59248756A JPS61127833A (en) 1984-11-27 1984-11-27 Recovery of mercury in iron sulfide concentrate

Publications (1)

Publication Number Publication Date
JPS61127833A true JPS61127833A (en) 1986-06-16

Family

ID=17182906

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59248756A Pending JPS61127833A (en) 1984-11-27 1984-11-27 Recovery of mercury in iron sulfide concentrate

Country Status (1)

Country Link
JP (1) JPS61127833A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001042519A1 (en) * 1999-12-09 2001-06-14 Geo2 Limited Recovery of precious metals
US6660059B2 (en) 2000-05-19 2003-12-09 Placer Dome Technical Services Limited Method for thiosulfate leaching of precious metal-containing materials
US7544232B2 (en) 2002-11-15 2009-06-09 Placer Dome Technical Services Ltd. Method for thiosulfate leaching of precious metal-containing materials
US9051625B2 (en) 2011-06-15 2015-06-09 Barrick Gold Corporation Method for recovering precious metals and copper from leach solutions
US10161016B2 (en) 2013-05-29 2018-12-25 Barrick Gold Corporation Method for pre-treatment of gold-bearing oxide ores
US10415116B2 (en) 2010-12-07 2019-09-17 Barrick Gold Corporation Co-current and counter current resin-in-leach in gold leaching processes

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654374A (en) * 1979-10-09 1981-05-14 Nec Corp Doppler detecting system of active sonar apparatus
JPS5693832A (en) * 1979-12-21 1981-07-29 Redondo Abad Angel Luis Recovery of nonferrous metal from sulfide ore
JPS5723041A (en) * 1980-06-03 1982-02-06 Min E Purodeyui Shimiku Do Sar Recovery of gold and / or silver and bismuth , if contained , contained in sulfide ore and / or sulfoarsenide

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654374A (en) * 1979-10-09 1981-05-14 Nec Corp Doppler detecting system of active sonar apparatus
JPS5693832A (en) * 1979-12-21 1981-07-29 Redondo Abad Angel Luis Recovery of nonferrous metal from sulfide ore
JPS5723041A (en) * 1980-06-03 1982-02-06 Min E Purodeyui Shimiku Do Sar Recovery of gold and / or silver and bismuth , if contained , contained in sulfide ore and / or sulfoarsenide

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001042519A1 (en) * 1999-12-09 2001-06-14 Geo2 Limited Recovery of precious metals
US6660059B2 (en) 2000-05-19 2003-12-09 Placer Dome Technical Services Limited Method for thiosulfate leaching of precious metal-containing materials
US7066983B2 (en) 2000-05-19 2006-06-27 Placer Dome Technical Services Limited Method for thiosulfate leaching of precious metal-containing materials
US7559974B2 (en) 2000-05-19 2009-07-14 Placer Dome Technical Services Ltd. Method for thiosulfate leaching of precious metal-containing materials
US7704298B2 (en) 2000-05-19 2010-04-27 Placer Dome Technical Services Limited Method for thiosulfate leaching of precious metal-containing materials
US7544232B2 (en) 2002-11-15 2009-06-09 Placer Dome Technical Services Ltd. Method for thiosulfate leaching of precious metal-containing materials
US10415116B2 (en) 2010-12-07 2019-09-17 Barrick Gold Corporation Co-current and counter current resin-in-leach in gold leaching processes
US9051625B2 (en) 2011-06-15 2015-06-09 Barrick Gold Corporation Method for recovering precious metals and copper from leach solutions
US10161016B2 (en) 2013-05-29 2018-12-25 Barrick Gold Corporation Method for pre-treatment of gold-bearing oxide ores
US10597752B2 (en) 2013-05-29 2020-03-24 Barrick Gold Corporation Method for pre-treatment of gold-bearing oxide ores
US11401580B2 (en) 2013-05-29 2022-08-02 Barrick Gold Corporation Method for pre-treatment of gold-bearing oxide ores

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