CN104785378A - Preparing method for tetrahedrite inhibitor - Google Patents

Preparing method for tetrahedrite inhibitor Download PDF

Info

Publication number
CN104785378A
CN104785378A CN201510227211.3A CN201510227211A CN104785378A CN 104785378 A CN104785378 A CN 104785378A CN 201510227211 A CN201510227211 A CN 201510227211A CN 104785378 A CN104785378 A CN 104785378A
Authority
CN
China
Prior art keywords
tetrahedrite
solution
inhibitor
mass ratio
water
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
CN201510227211.3A
Other languages
Chinese (zh)
Inventor
魏宗武
杨雄斌
杜盼
邓建
黄威
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.)
Guangxi University
Original Assignee
Guangxi University
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 Guangxi University filed Critical Guangxi University
Priority to CN201510227211.3A priority Critical patent/CN104785378A/en
Publication of CN104785378A publication Critical patent/CN104785378A/en
Pending legal-status Critical Current

Links

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Abstract

A preparing method for a tetrahedrite inhibitor comprises the following steps that oxalic acid, sodium sulfite and water are mixed to obtain a solution 1 according to the mass proportion of oxalic acid, sodium sulfite and water being 2-3:3-4:6-8, waxberry tannin extract is added in the solution 1 according to the mass ratio of 1-2:3-7, and the mixture is stirred and dissolved to obtain a solution 2; calcium thioglycolatetrihydrate is added in the solution 2 according to the mass ratio of 1-2:1-5, the temperature of the solution 2 is controlled to range from 70 DEG C to 75 DEG C, the stirring reaction is kept for 1-1.5 h to obtain a solution 3, the solution 3 is sucked and filtered to obtain a viscous material, finally, the viscous material is dried under the temperature of 70-75 DEG C, and then the tetrahedrite inhibitor is obtained. The tetrahedrite can be restrained through the inhibitor prepared through the method, the copper pyrites and tetrahedrite are separated through floatation, and the content of antimony in copper concentrate is reduced.

Description

A kind of preparation method of tetrahedrite inhibitor
One, technical field
The present invention relates to a kind of preparation method of tetrahedrite inhibitor, in the copper concentrate particularly coexisted for chalcopyrite and tetrahedrite, suppresses preparation method and the application thereof of a kind of inhibitor of tetrahedrite when need reduce antimony content in copper concentrate.
Two, background technology
In some brass mineral deposits, usually contain other as other association copper sulfide minerals such as covellite, chalmersite, tetrahedrites, for the recovery of this kind of copper sulfide ore, current technique of preparing is quite ripe, and technical process is also comparatively simple.On the one hand the floatability of copper sulfide mineral is better, and on the other hand, in impure mineral except pyrite, mispickel etc. have certain interference to copper sulfide mineral flotation, other can not have an impact to copper sulfide mineral as the impure mineral such as silicon, calcium.Due to the existence of antimony in tetrahedrite, when electrolysis, overwhelming majority antimony exists in the form of an oxide, and in anodic dissolution processes, there occurs series reaction with the antimony that oxide form exists, they finally form oxide solid particulate, or be attached to anode surface, or being suspended in electrolyte, this type of solid matter, after disengaging anode surface, pollutes cathode copper at negative electrode mechanical entrainment.If removed by the antimony in copper concentrate before smelting, greatly electrolytic copper quality will be improved undoubtedly.
Three, summary of the invention
The object of the present invention is to provide a kind of preparation method of tetrahedrite inhibitor, the prepared inhibitor obtained can suppress the tetrahedrite in chalcopyrite and tetrahedrite bulk concentrate, reduces the antimony content in copper concentrate.
The present invention achieves the above object by the following technical solutions: a kind of preparation method of tetrahedrite inhibitor, comprise the steps: first to be oxalic acid in mass ratio by oxalic acid, sodium sulfite and water: sodium sulfite: water=2 ~ 3:3 ~ 4:6 ~ 8 are mixed to get solution 1, then myrica extract in mass ratio=1 ~ 2:3 ~ 7 are added in solution 1, be stirred to and dissolve to obtain solution 2; Then calcium mercaptoacetate in mass ratio=1 ~ 2:1 ~ 5 are added in solution 2, controlling solution 2 temperature is 70 ~ 75 DEG C, and stirring reaction keeps 1 ~ 1.5h to obtain solution 3, and solution 3 suction filtration is obtained dope, finally that dope is dry under 70 ~ 75 DEG C of conditions, be described tetrahedrite inhibitor.
During flotation, slurry pH is 7.5 ~ 8; In floatation process, the bulk concentrate of chalcopyrite and tetrahedrite is added water after stirring, add described inhibitor, collecting agent.
The total consumption of described inhibitor is: 350 ~ 400g/t.
Unless otherwise indicated, percentage of the present invention is mass percent, and each constituent content percentage sum is 100%.
Concrete advantage of the present invention is:
1, the inhibitor adopting the present invention to be prepared into can suppress tetrahedrite, reduces antimony content in copper concentrate.
2, dosing is few.
Four, detailed description of the invention
Below by way of specific embodiment, technical scheme of the present invention is further described.
Embodiment 1
An example of the preparation method of a kind of tetrahedrite inhibitor of the present invention, comprises the following steps:
First by oxalic acid, sodium sulfite and water oxalic acid in mass ratio: sodium sulfite: water=2:3:6 is mixed to get solution 1, then by myrica extract in mass ratio=1:3 adds in solution 1, be stirred to and dissolve to obtain solution 2; Then calcium mercaptoacetate in mass ratio=1:1 adds in solution 2, controlling solution 2 temperature is 70 DEG C, and stirring reaction keeps 1h to obtain solution 3, and solution 3 suction filtration is obtained dope, finally that dope is dry under 70 DEG C of conditions, namely obtains described tetrahedrite inhibitor.
Embodiment 2
Another example of the preparation method of a kind of tetrahedrite inhibitor of the present invention, comprises the following steps:
First by oxalic acid, sodium sulfite and water oxalic acid in mass ratio: sodium sulfite: water=3:4:8 is mixed to get solution 1, then by myrica extract in mass ratio=2:7 adds in solution 1, be stirred to and dissolve to obtain solution 2; Then by calcium mercaptoacetate in mass ratio=2:5 adds in solution 2, controlling solution 2 temperature is 75 DEG C, and stirring reaction keeps 1.5h to obtain solution 3, and solution 3 suction filtration is obtained dope, finally that dope is dry under 75 DEG C of conditions, namely obtains described tetrahedrite inhibitor.
Embodiment 3
The present embodiment is the application example of described tetrahedrite inhibitor in chalcopyrite and tetrahedrite FLOTATION SEPARATION.
1, raw mineral materials:
Raw mineral materials chalcopyrite used and tetrahedrite bulk concentrate, wherein copper content is 30.11%, antimony content is 5.53%, sulfur content is 25.72%, iron content is 15.41%, show through material phase analysis, mainly exist with chalcopyrite, tetrahedrite form in bulk concentrate, separately have a small amount of chalmersite and magnesia, calcium carbonate mineral.
2, regime of agent and operating condition: adjust pH values of pulp to 7.5 ~ 8, by inhibitor 350g/t with sodium carbonate, diethyldithiocarbamate 50g/t dosing is tested, result shows to adopt above agentia condition can effectively by chalcopyrite and tetrahedrite FLOTATION SEPARATION, under being 5.53% condition to ore deposit antimony content, scan and triple cleaning through one roughing secondary, in flotation concentrate, the content of antimony is reduced to 0.65%.
Embodiment 4
The present embodiment is the Another Application example of described tetrahedrite inhibitor in chalcopyrite and tetrahedrite FLOTATION SEPARATION.
1, raw mineral materials:
Raw mineral materials chalcopyrite used and tetrahedrite bulk concentrate, wherein copper content is 32.80%, antimony content is 6.04%, sulfur content is 23.47%, iron content is 12.54%, show through material phase analysis, mainly exist with chalcopyrite, tetrahedrite form in bulk concentrate, separately have a small amount of chalmersite and magnesia, calcium carbonate mineral.
2, regime of agent and operating condition: adjust pH values of pulp to 7.5 ~ 8, by inhibitors 4 00g/t with sodium carbonate, diethyldithiocarbamate 50g/t dosing is tested, result shows to adopt above agentia condition can effectively by chalcopyrite and tetrahedrite FLOTATION SEPARATION, under being 6.04% condition to ore deposit antimony content, scan and triple cleaning through one roughing secondary, the content of flotation concentrate antimony is reduced to 0.72%.

Claims (3)

1. the preparation method of a tetrahedrite inhibitor, it is characterized in that, comprise the steps: first to be oxalic acid in mass ratio by oxalic acid, sodium sulfite and water: sodium sulfite: water=2 ~ 3:3 ~ 4:6 ~ 8 are mixed to get solution 1, then myrica extract in mass ratio=1 ~ 2:3 ~ 7 are added in solution 1, be stirred to and dissolve to obtain solution 2; Then calcium mercaptoacetate in mass ratio=1 ~ 2:1 ~ 5 are added in solution 2, controlling solution 2 temperature is 70 ~ 75 DEG C, and stirring reaction keeps 1 ~ 1.5h to obtain solution 3, and solution 3 suction filtration is obtained dope, finally that dope is dry under 70 ~ 75 DEG C of conditions, be described tetrahedrite inhibitor.
2. the application of tetrahedrite inhibitor according to claim 1 in chalcopyrite and tetrahedrite FLOTATION SEPARATION, is characterized in that, during flotation, slurry pH is 7.5 ~ 8; In floatation process, the bulk concentrate of chalcopyrite and tetrahedrite is added water after stirring, adds described inhibitor, collecting agent,
The total consumption of described inhibitor is: 200 ~ 300g/t.
3. the application of tetrahedrite inhibitor according to claim 2 in chalcopyrite and tetrahedrite FLOTATION SEPARATION, is characterized in that, during use, described inhibitor is first mixed with the aqueous solution that mass percentage concentration is 1%.
CN201510227211.3A 2015-05-06 2015-05-06 Preparing method for tetrahedrite inhibitor Pending CN104785378A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510227211.3A CN104785378A (en) 2015-05-06 2015-05-06 Preparing method for tetrahedrite inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510227211.3A CN104785378A (en) 2015-05-06 2015-05-06 Preparing method for tetrahedrite inhibitor

Publications (1)

Publication Number Publication Date
CN104785378A true CN104785378A (en) 2015-07-22

Family

ID=53550832

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510227211.3A Pending CN104785378A (en) 2015-05-06 2015-05-06 Preparing method for tetrahedrite inhibitor

Country Status (1)

Country Link
CN (1) CN104785378A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4643823A (en) * 1982-09-10 1987-02-17 Phillips Petroleum Company Recovering metal sulfides by flotation using mercaptoalcohols
CN1032630A (en) * 1987-10-20 1989-05-03 广西冶金研究所 The separating technology of antimony sulfide ore-mispickel and the medicament of use thereof
CN101069875A (en) * 2007-06-12 2007-11-14 长春黄金研究院 Composite inhibitor for inhibiting arsenic ore floatation

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4643823A (en) * 1982-09-10 1987-02-17 Phillips Petroleum Company Recovering metal sulfides by flotation using mercaptoalcohols
CN1032630A (en) * 1987-10-20 1989-05-03 广西冶金研究所 The separating technology of antimony sulfide ore-mispickel and the medicament of use thereof
CN101069875A (en) * 2007-06-12 2007-11-14 长春黄金研究院 Composite inhibitor for inhibiting arsenic ore floatation

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
李宗站 等: "国内铜硫浮选分离研究现状", 《金属矿山》 *

Similar Documents

Publication Publication Date Title
CN101204681B (en) Method of refining iron ore from alkaline red mud and making gangue neutral
AU2011211739B2 (en) Method for separating arsenic mineral from copper material with high arsenic content
JP4450108B1 (en) Separation of arsenic minerals from high arsenic grade copper-containing materials
CN101947496B (en) Preparation method of copper-zinc sulfide ore flotation separation inhibitor and application thereof
CN104525384B (en) Preparation method of inhibitor of limonite
WO2021128922A1 (en) Application of 2-(3-substituted ureido)-n-hydroxy-2-oxoacetimide cyanide compound in flotation
CN102527497B (en) Beneficiation method for separating zinc sulfide ores from sulphur in wet-method zinc smelting slag
CN103691574B (en) A kind of preparation method of dolomite inhibitor and application thereof
CN102671771A (en) Method for floating and separating zinc silicate and kutnahorite
CN107185724A (en) A kind of method for floating that gold sulphide ores are reclaimed from tailings
CN113333178A (en) Gold ore flotation collector and preparation method thereof
JP5774374B2 (en) Method for separating arsenic mineral from copper-containing material containing arsenic mineral
CN107185705A (en) Dressing and smelting combined recovery method for zinc in zinc oxide ore
CN104785378A (en) Preparing method for tetrahedrite inhibitor
CN103071597B (en) Preparation method of high-purity copper sulfide
CN102784722B (en) Flotation process for cyanide tailings in silver concentrates
CN106216101B (en) Method for improving recovery rate of sulfur and gold in tailings of old tailings pond
CN105127008A (en) Method for preparing stibnite inhibitor
CN106238217A (en) A kind of preparation method of zinc oxide ore collecting agent
CN104437888A (en) Method for preparing zinc-sulfur mineral depressor
CN103774178A (en) Additive for electrolyzing manganese from manganese sulfate electrolyte system and application method of additive
CN102489408A (en) Flotation method for separating copper form mica
CN103657860B (en) The method of reverse flotation enrichment zinc silicate mineral in acid condition
CN112427145A (en) Flotation separation method for galena and pyrite
CN110899000A (en) Combined collecting agent for flotation decalcification of magnesite and application thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
EXSB Decision made by sipo to initiate substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20150722