CN106269281B - A kind of preparation method of Wolframite agent - Google Patents

A kind of preparation method of Wolframite agent Download PDF

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Publication number
CN106269281B
CN106269281B CN201610629954.8A CN201610629954A CN106269281B CN 106269281 B CN106269281 B CN 106269281B CN 201610629954 A CN201610629954 A CN 201610629954A CN 106269281 B CN106269281 B CN 106269281B
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wolframite
agent
stirred
solution
mass ratio
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CN106269281A (en
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艾光华
涂燕琼
杨冰
罗丽芳
蔡鑫
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Jiangxi University of Science and Technology
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Jiangxi University of Science and Technology
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/018Mixtures of inorganic and organic compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/02Collectors

Abstract

A kind of preparation method of Wolframite agent, includes the following steps:First in mass ratio=1~2 by oleic acid and sodium methanesulfonate:1~3 is stirred 1 hour to obtain solution 1 at normal temperatures, then in mass ratio=1~2 by ethylenediamine:3~7 are slowly added in solution 1, and 2.5~3 hours obtained solutions 2 are stirred to react under the conditions of 85~90 DEG C of temperature, finally again plus mass percentage concentration be 10~15% sodium hydroxide neutralize after the translucent thick liquid of brown color of gained be the Wolframite agent.

Description

A kind of preparation method of Wolframite agent
One, technical field
The present invention relates to a kind of preparation methods of Wolframite agent, especially for the system of Wolframite collecting agent Preparation Method.
Two, background technology
It is typically all both at home and abroad at present to be recycled using gravity separation method to the ore dressing of coarse grain wolframite, the rate of recovery of wolframite is most 45% hereinafter, loss late is larger;To the wolframite of fine fraction wolframite especially micro-size fraction, domestic and international ore dressing is main at present With gravity treatment, the methods of again-floating process integration Wolframite is recycled, but since complex process or floating agent select Property is not strong, does not still find preferable recovery method at present.For wolframite fine size, grade is low, contains in gangue mineral A large amount of quartz and thin mud, the annual fine fraction wolframite value being lost in tailing is tens billion of, as can will be micro- using method for floating Fine wolframite is detached with other impure minerals, this has important practical significance to the recycling of wolframite resource.
Three, invention content
The purpose of the present invention is to provide a kind of preparation method of Wolframite agent, the collecting agent being prepared into this method It can realize that wolframite efficient flotation separation recycles.
The present invention realizes above-mentioned purpose using following technical scheme:A kind of preparation method of Wolframite agent, including such as Lower step:First in mass ratio=1~2 by oleic acid and sodium methanesulfonate:1~3 is stirred 1 hour to obtain solution 1 at normal temperatures, Then in mass ratio=1~2 by ethylenediamine:3~7 are slowly added in solution 1, are stirred to react under the conditions of 85~90 DEG C of temperature 2.5~3 hours obtained solutions 2, the brown color of gained after finally adding the sodium hydroxide of mass percentage concentration 10~15% to neutralize again Translucent thick liquid is the Wolframite agent.
Slurry pH is 9~9.5 when flotation;In floatation process, gangue is added after ore ore grinding to mineral monomer is dissociated Inhibitor 800~1000g/t of waterglass, then be added activator 300~400g/t of plumbi nitras, then add the collecting agent 800~ 1000g/t, finally plus the agent 110~130g/t of 2# oil that spumes carries out collecting to wolframite.
In use, the collecting agent is first configured to 10% solution.
Unless otherwise stated, percentage of the present invention is mass percent, and the sum of each component content percentage is 100%.
Particularly advantage of the invention is:
1, using the collecting agent that is prepared into of the present invention can collecting wolframite, it is soluble easily in water, and have good selectivity And resistance to low temperature.
2, dosing is few.
Four, specific implementation mode
Technical scheme of the present invention is further described below by way of specific embodiment.
Embodiment 1
One example of the preparation method of Wolframite agent of the present invention, includes the following steps:
First in mass ratio=1 by oleic acid and sodium methanesulfonate:1 is stirred 1 hour to obtain solution 1 at normal temperatures, then In mass ratio=1 by ethylenediamine:3 are slowly added in solution 1, are stirred to react under the conditions of temperature is 85 DEG C and are made within 2.5 hours molten Liquid 2, the translucent thick liquid of brown color of gained is institute after finally mass percentage concentration being added to be neutralized for 10% sodium hydroxide again State Wolframite agent.
Embodiment 2
Another example of the preparation method of Wolframite agent of the present invention, includes the following steps:
First in mass ratio=2 by oleic acid and sodium methanesulfonate:3 are stirred 1 hour to obtain solution 1 at normal temperatures, then In mass ratio=2 by ethylenediamine:7 are slowly added in solution 1, and 3 hours obtained solutions 2 are stirred to react under the conditions of 90 DEG C of temperature, The translucent thick liquid of brown color of gained is described black after finally the sodium hydroxide that mass percentage concentration is 15% being added to neutralize again Tungsten ore collecting agent.
Embodiment 3
The present embodiment is an application example of the Wolframite agent in Flotation Wolframite.
1, raw mineral materials:
W content is 0.37% in ore used, dioxide-containing silica 13.54%, iron content 15.75%, object phase point Analysis shows that tungsten mainly exists in the form of wolframite, separately there is a small amount of scheelite;Gangue mineral mainly exists with silicate patterns, separately There are segment magnet mine and goethite.
2. floating agent and operating condition:
In floatation process, after ore ore grinding to mineral monomer is dissociated, sodium carbonate is added and disperses and inhibit arteries and veins with waterglass Stone ore object, then plumbi nitras is added to activate wolframite, finally plus the collecting agent carries out collecting to wolframite and obtains tungsten concentrate product.Experiment The result shows that can effectively recycle wolframite using process above and agentia condition;Under the conditions of being 0.37% to mine W content, Scanned twice by one roughing it is selected twice, obtain tungstic acid content be 54.21%, the tungsten concentrate of the rate of recovery 79.57%.
Embodiment 4
The present embodiment is that the Wolframite agent floats on the another application example in Flotation Wolframite.
1, raw mineral materials:
W content is 0.40% in ore used, dioxide-containing silica 17.65%, iron content 14.06%, object phase point Analysis shows that tungsten mainly exists in the form of wolframite, separately there is a small amount of scheelite;Gangue mineral mainly exists with silicate patterns, separately There are segment magnet mine and goethite.
2. floating agent and operating condition:
In floatation process, after ore ore grinding to mineral monomer is dissociated, sodium carbonate is added and disperses and inhibit arteries and veins with waterglass Stone ore object, then plumbi nitras is added to activate wolframite, finally plus the collecting agent carries out collecting to wolframite and obtains tungsten concentrate product.Experiment The result shows that can effectively recycle wolframite using process above and agentia condition;Under the conditions of being 0.40% to mine W content, Scanned twice by one roughing it is selected twice, obtain tungstic acid content be 56.77%, the tungsten concentrate of the rate of recovery 81.24%.

Claims (3)

1. a kind of preparation method of Wolframite agent, which is characterized in that include the following steps:First by oleic acid and pyrovinic acid Sodium is in mass ratio=1~2:1~3 is stirred 1 hour to obtain solution 1 at normal temperatures, then in mass ratio=1~2 by ethylenediamine:3 ~7 are slowly added in solution 1, and 2.5~3 hours obtained solutions 2 are stirred to react under the conditions of 85~90 DEG C of temperature, finally again plus matter The translucent thick liquid of brown color of gained is the Wolframite after the sodium hydroxide of amount percentage concentration 10~15% neutralizes Agent.
2. application of the Wolframite agent described in claim 1 in Flotation Wolframite, which is characterized in that pH values of pulp when flotation Value is 9~9.5;In floatation process, gangue inhibitor waterglass 800~1000 is added after ore ore grinding to mineral monomer is dissociated Then g/t is added 300~400 g/t of activator plumbi nitras, then adds 800~1000 g/t of Wolframite agent, finally add 110~130 g/t of agent 2# oil that spumes carries out collecting to wolframite.
3. application of the Wolframite agent according to claim 2 in Flotation Wolframite, which is characterized in that in use, The Wolframite agent is configured to 10% solution.
CN201610629954.8A 2016-05-12 2016-08-04 A kind of preparation method of Wolframite agent Active CN106269281B (en)

Applications Claiming Priority (2)

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CN201610312338 2016-05-12
CN201610312338X 2016-05-12

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CN106269281B true CN106269281B (en) 2018-07-27

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110564962B (en) * 2019-10-14 2020-12-22 中南大学 Smelting method of black-white tungsten mixed ore

Citations (5)

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Publication number Priority date Publication date Assignee Title
SU1645024A1 (en) * 1989-05-31 1991-04-30 Казахский государственный университет им.С.М.Кирова Flotation of rare metal and tin ores
CN102125891A (en) * 2010-12-07 2011-07-20 鞍钢集团矿业公司 Method for making magnet-red iron mixed ore anionic reverse flotation catching agent
CN104525384A (en) * 2015-01-08 2015-04-22 广西大学 Preparation method of inhibitor of limonite
CN104815762A (en) * 2015-05-06 2015-08-05 广西大学 Method for preparing tennantite collecting agent
CN105170338A (en) * 2015-08-28 2015-12-23 张好勇 Non-sulfide mineral flotation collector, preparation method thereof and application thereof

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Publication number Priority date Publication date Assignee Title
PE20130498A1 (en) * 2010-01-14 2013-04-22 Teebee Holdings Pty Ltd FLOTATION REAGENTS

Patent Citations (5)

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Publication number Priority date Publication date Assignee Title
SU1645024A1 (en) * 1989-05-31 1991-04-30 Казахский государственный университет им.С.М.Кирова Flotation of rare metal and tin ores
CN102125891A (en) * 2010-12-07 2011-07-20 鞍钢集团矿业公司 Method for making magnet-red iron mixed ore anionic reverse flotation catching agent
CN104525384A (en) * 2015-01-08 2015-04-22 广西大学 Preparation method of inhibitor of limonite
CN104815762A (en) * 2015-05-06 2015-08-05 广西大学 Method for preparing tennantite collecting agent
CN105170338A (en) * 2015-08-28 2015-12-23 张好勇 Non-sulfide mineral flotation collector, preparation method thereof and application thereof

Non-Patent Citations (2)

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