CN109439923A - A kind of extraction auxiliary agent can be improved gold solution rate - Google Patents
A kind of extraction auxiliary agent can be improved gold solution rate Download PDFInfo
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- CN109439923A CN109439923A CN201811578160.9A CN201811578160A CN109439923A CN 109439923 A CN109439923 A CN 109439923A CN 201811578160 A CN201811578160 A CN 201811578160A CN 109439923 A CN109439923 A CN 109439923A
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- gold
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- auxiliary agent
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- solution rate
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B11/00—Obtaining noble metals
- C22B11/08—Obtaining noble metals by cyaniding
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/04—Extraction of metal compounds from ores or concentrates by wet processes by leaching
- C22B3/12—Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic alkaline solutions
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
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Abstract
The invention discloses a kind of extraction auxiliary agent that can be improved gold solution rate, the auxiliary agent includes the raw material of following parts by weight: 3-8 parts of sodium potassium tartrate tetrahydrate, 3-8 parts of ammonium citrate, 2-4 parts of soda ash, 2-3 parts of sodium lignin sulfonate, 1-2 parts of lead salt and 4-8 parts of sulfonation nitrobenzene.The usage amount of the auxiliary agent is auxiliary agent and the mass ratio of gold ore agent is 2-10:100-180.Gold provided by the invention extracts auxiliary agent and is added in gold ore agent, the solution rate of gold is obviously accelerated, dissolution time greatly shortens, improve the production efficiency of gold, improve place service efficiency, there is good social benefit, ecological benefits and economic benefit for Gold Industry, be suitble to large-scale promotion.
Description
Technical field
The present invention relates to metallurgical industry processing technology field, specifically a kind of extraction that can be improved gold solution rate is helped
Agent.
Background technique
In golden production industry, extraction of gold by cyanidation is generallyd use at present.During cyanidation gold-extracted, gold solution rate
Speed, two broad aspects are depended primarily on, first is that the size of the contact area of gold and gold leaching solution, second is that in gold leaching solution
The concentration of dissolved oxygen.In order to improve the rate of recovery of gold, the grinding rate of ore generally all using extraction time is extended, is improved in various regions
Etc. modes realize, cause the period entirely produced long.Production technology is drenched for pond leaching or heap, a production cycle is often
It requires to take a month time of 3-6;And production technology is starched for carbon, the production cycle is mostly at 30 more than hour.Therefore, raw
Produce the universal phenomenon that period length is this industry.
In gold dust or rock gold mine containing bright gold, golden particle be often it is bigger, most of gold is all exposed
Comparison it is sufficient.For this kind of ore, common processing method is to use gravity separation method, fewer to use cyaniding, because if
It is taken a long time with cyaniding and needs to be leached, can guarantee all dissolution recycling of more coarse grained gold.
And gravity separation method also has limitation, for the bright gold that some quilts partly wrap up, is not easy to smoothly select, and causes tailings grade to run high.
In electronic component and waste and old circuit board gold refinement industry, since this kind of object outer dimension is not of uniform size, using pond leaching or
Spray process, primary treating capacity is simultaneously few, and the extraction time equally consumed is very long, causes production efficiency not high.
Therefore, during golden production, it is badly in need of a kind of solution rate that can accelerate gold now, shortens extraction time
Extraction auxiliary agent.
The disclosure of background above technology contents is only used for auxiliary and understands inventive concept and technical solution of the invention, not
The prior art for necessarily belonging to present patent application shows above content in the applying date of present patent application in no tangible proof
In the case where having disclosed, above-mentioned background technique should not be taken to the novelty and creativeness of evaluation the application.
Summary of the invention
The present invention has that solution rate is slow, extraction time is grown for existing gold extraction process, provides a kind of energy
Solution rate is improved, extraction time is greatly shortened, the gold for accelerating production efficiency extracts auxiliary agent.
In order to achieve the goal above, The technical solution adopted by the invention is as follows:
A kind of extraction auxiliary agent can be improved gold solution rate, the auxiliary agent include the raw material of following parts by weight: tartaric acid
3-8 parts of potassium sodium, 3-8 parts of ammonium citrate, 2-4 parts of soda ash, 2-3 parts of sodium lignin sulfonate, 1-2 parts of lead salt and sulfonation nitrobenzene 4-8
Part.
Preferably, the lead salt include one of plumbi nitras, lead acetate, lead chloride, lead sulfate and basic lead carbonate or
Multiple combinations.
Preferably, it is 2-10:100-180 that the usage amount of the auxiliary agent, which is the mass ratio of auxiliary agent and gold ore agent,.
Preferably, the gold ore agent is the gold ore agent of golden cicada board.
Preferably, the auxiliary agent independent packaging or with the hybrid packed use of gold ore agent.
Preferably, the auxiliary agent by 5 parts of sodium potassium tartrate tetrahydrate, 6 parts of ammonium citrate, 2.5 parts of soda ash, 3 parts of sodium lignin sulfonate,
1.5 parts and 7 parts of sulfonation nitrobenzene of lead acetate;The mass ratio 1:18 of auxiliary agent and gold ore agent when use.
Compared with prior art, it advantages of the present invention and has the beneficial effect that
1, gold provided by the invention extracts auxiliary agent (abbreviation HDGSQ) and is added in gold ore agent, and the solution rate of gold is bright
Aobvious to accelerate, dissolution time greatly shortens, and improves the production efficiency of gold, improves place service efficiency.
2, HDGSQ is added in gold ore agent, compared with Cymag, under the conditions of same dosage, HDGSQ auxiliary agent of the present invention makes
The solution rate for obtaining gold significantly improves, and dissolution time significantly shortens, and will not reduce the recovery rate of gold, and cost is relatively low.
Therefore HDGSQ provided by the invention has good social benefit, ecological benefits and economic benefit for Gold Industry, is suitble to big
Scale is promoted.
Specific embodiment
Invention is further described in detail With reference to embodiment.It is emphasized that following the description is only
It is merely exemplary, the range and its application being not intended to be limiting of the invention.
Embodiment 1
(1) HDGSQ auxiliary agent 2g, golden cicada board gold ore agent 36g is taken to be added in 500mL water, stirring and dissolving, obtain molten auri
Plinth solution A.The HDGSQ auxiliary agent is by 4 parts of sodium potassium tartrate tetrahydrate, 6 parts of ammonium citrate, 3.5 parts of soda ash, 3 parts of sodium lignin sulfonate, nitre
1.5 parts and 6 parts of sulfonation nitrobenzene of lead plumbate.
(2) 38 grams of Cymag are taken, is added in 500mL water, stirring and dissolving, molten gold base solution B is obtained.
(3) take the waste and old phonecard of two panels (its surface is coated with one layer of gold), put into respectively above-mentioned molten gold base solution A and
In B, slightly shakes frequently and make a movement phonecard or mix up solution.
(4) the gold dissolution situation on phonecard surface is observed, the dissolvd gold speed of two kinds of molten gold base solution is compared.
Solution rate observation: after two minutes, it can be seen that, the gold on phonecard surface is in molten gold base solution A
It dissolves more than half;And the gold on the phonecard surface in molten gold base solution B yet there are no apparent dissolution.It is further continued for observing, five points
After clock, it can be seen that, the gold on phonecard surface has been completely dissolved in molten gold base solution A;And in molten gold base solution B
The gold on phonecard surface originates the existing sign slightly dissolved.It has crossed after ten hours, the phonecard table in molten gold base solution B
Just basic dissolution finishes the gold in face.
It can be seen that in the drug solution of higher concentration, added with HDGSQ additive golden cicada board gold ore agent solution A it is molten
Golden speed greatly exceeds the dissolvd gold speed of the sodium cyanide solution B of same drug concentration, and the molten temporal difference of gold of the two is more than
Ten times or more.
Embodiment 2
(1) HDGSQ auxiliary agent 0.1g, golden cicada board gold ore agent 1.8g is taken to be added in 500mL water, stirring and dissolving, obtain molten gold
Base soln A.The HDGSQ auxiliary agent by 7 parts of sodium potassium tartrate tetrahydrate, 5 parts of ammonium citrate, 2.5 parts of soda ash, 2 parts of sodium lignin sulfonate,
2 parts and 7 parts of sulfonation nitrobenzene of lead acetate.
(2) 1.9 grams of Cymag are taken, is added in 500mL water, stirring and dissolving, molten gold base solution B is obtained.
(3) take the waste and old phonecard of two panels (its surface is coated with one layer of gold), put into respectively above-mentioned molten gold base solution A and
In B, slightly shakes frequently and make a movement phonecard or mix up solution.
(4) the gold dissolution situation on phonecard surface is observed, the dissolvd gold speed of two kinds of molten gold base solution is compared.
Solution rate observation: it after 15 minutes, can see in molten gold base solution A, the gold on phonecard surface
It has dissolved more than half;And the gold on the phonecard surface in molten gold base solution B yet there are no apparent dissolution.It is further continued for observing, half
After a hour, it can be seen that, the gold on phonecard surface has been completely dissolved in molten gold base solution A;And molten gold base solution B
In the gold on phonecard surface originate the existing sign slightly dissolved.It has crossed after 18 hours, the electricity in molten gold base solution B
Just basic dissolution finishes the gold on words card surface.
As it can be seen that in the drug solution of low concentration, although molten gold base solution A has dropped the solution rate of gold,
However, it will be apparent that, it is also still greatly exceeded added with the dissolvd gold speed of the golden cicada board gold ore agent solution B of HDGSQ additive
The dissolvd gold speed of the sodium cyanide solution B of same drug concentration.
Embodiment 3
(1) HDGSQ auxiliary agent 1g, golden cicada board gold ore agent 20g is taken to be added in 500mL water, stirring and dissolving, obtain molten auri
Plinth solution A.The HDGSQ auxiliary agent is by 5 parts of sodium potassium tartrate tetrahydrate, 6 parts of ammonium citrate, 2.5 parts of soda ash, 3 parts of sodium lignin sulfonate, second
1.5 parts and 7 parts of sulfonation nitrobenzene of lead plumbate.
(2) 21 grams of Cymag are taken, is added in 500mL water, stirring and dissolving, molten gold base solution B is obtained.
(3) it takes two panels to contain golden waste and old circuit board, puts into above-mentioned molten gold base solution A and B, slightly shake frequently respectively
Once circuit board or mix up solution.
(4) the gold dissolution situation on circuit board surface is observed, the dissolvd gold speed of two kinds of molten gold base solution is compared.
Solution rate observation: after five minutes, it can be seen that, the gold on waste and old circuit board is in molten gold base solution A
It dissolves more than half;And the gold of the waste and old circuit board in molten gold base solution B yet there are no apparent dissolution.It is further continued for observing, half
After hour, it can be seen that, the gold of waste and old circuit board has been completely dissolved in molten gold base solution A;And in molten gold base solution B
The gold of waste and old circuit board originate the existing sign slightly dissolved.It has crossed after five hours, the phonecard in molten gold base solution B
Just basic dissolution finishes the gold on surface.
As it can be seen that in the drug solution of higher concentration, added with the golden cicada board gold ore agent solution B of HDGSQ additive
Dissolvd gold speed also still greatly exceeds the dissolvd gold speed of the sodium cyanide solution B of same drug concentration.
Embodiment 4
(1) HDGSQ auxiliary agent 0.2g, golden cicada board gold ore agent 10g is taken to be added in 500mL water, stirring and dissolving, obtain molten gold
Base soln A.The HDGSQ auxiliary agent by 6 parts of sodium potassium tartrate tetrahydrate, 4 parts of ammonium citrate, 2 parts of soda ash, 2.5 parts of sodium lignin sulfonate,
2 parts and 5 parts of sulfonation nitrobenzene of lead chloride.
(2) 10.2 grams of Cymag are taken, is added in 500mL water, stirring and dissolving, molten gold base solution B is obtained.
(3) it takes two panels to contain the gold dust of bright gold, puts into above-mentioned molten gold base solution A and B, mix up molten respectively
Liquid.
(4) the gold dissolution recovering state for observing gold dust, compares the dissolvd gold speed of two kinds of molten gold base solution.
Solution rate observation: after ten minutes, it can be seen that, gold dust has dissolved more than half in molten gold base solution A;And it is molten
The gold of gold dust yet there are no apparent dissolution in gold base solution B.It is further continued for observing, it is molten in molten gold base after two hours
It can be seen that, gold dust has been completely dissolved in liquid A;And the gold dust in molten gold base solution B starts to find there is the sign slightly dissolved.
It has crossed after 15 hours, just dissolution finishes the gold dust in molten gold base solution B substantially.
As it can be seen that in the drug solution of higher concentration, added with the golden cicada board gold ore agent solution B of HDGSQ additive
Dissolvd gold speed also still greatly exceeds the dissolvd gold speed of the sodium cyanide solution B of same drug concentration.
The above content is combine it is specific/further detailed description of the invention for preferred embodiment, cannot
Assert that specific implementation of the invention is only limited to these instructions.General technical staff of the technical field of the invention is come
It says, without departing from the inventive concept of the premise, some replacements or modifications can also be made to the embodiment that these have been described,
And these substitutions or variant are regarded as belonging to the scope of protection of the present invention.
Claims (6)
1. a kind of extraction auxiliary agent that can be improved gold solution rate, it is characterised in that: the auxiliary agent includes following parts by weight
Raw material: 3-8 parts of sodium potassium tartrate tetrahydrate, 3-8 parts of ammonium citrate, 2-4 parts of soda ash, 2-3 parts of sodium lignin sulfonate, 1-2 parts of lead salt and
4-8 parts of sulfonation nitrobenzene.
2. can be improved the extraction auxiliary agent of gold solution rate according to claim 1, it is characterised in that: the lead salt includes
One of plumbi nitras, lead acetate, lead chloride, lead sulfate and basic lead carbonate or multiple combinations.
3. the extraction auxiliary agent according to claim 1 or claim 2 that can be improved gold solution rate, it is characterised in that: the auxiliary agent
Usage amount be the mass ratio of auxiliary agent and gold ore agent be 2-10:100-180.
4. can be improved the extraction auxiliary agent of gold solution rate according to claim 3, it is characterised in that: the gold ore
Agent is the gold ore agent of golden cicada board.
5. can be improved the extraction auxiliary agent of gold solution rate according to claim 3, it is characterised in that: the auxiliary agent is independent
Packaging or with the hybrid packed use of gold ore agent.
6. can be improved the extraction auxiliary agent of gold solution rate according to claim 1, it is characterised in that: the auxiliary agent is by wine
5 parts of stone acid potassium sodium, 6 parts of ammonium citrate, 2.5 parts of soda ash, 3 parts of sodium lignin sulfonate, 1.5 parts of lead acetate and 7 parts of sulfonation nitrobenzene;
The mass ratio 1:18 of auxiliary agent and gold ore agent when use.
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Cited By (3)
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CN110257645A (en) * | 2019-05-28 | 2019-09-20 | 西北矿冶研究院 | Oxidation leaching agent for low-grade gold oxide ore and application process thereof |
CN110714120A (en) * | 2019-09-30 | 2020-01-21 | 广西森合高新科技股份有限公司 | Beneficiation auxiliary agent for gold beneficiation |
CN111089934A (en) * | 2020-01-13 | 2020-05-01 | 南京市产品质量监督检验院 | Method for measuring cyanide content in gold product by using ion chromatography technology |
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CN111089934A (en) * | 2020-01-13 | 2020-05-01 | 南京市产品质量监督检验院 | Method for measuring cyanide content in gold product by using ion chromatography technology |
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