CN101850305A - Novel mica inhibitor and preparation method and use method thereof - Google Patents
Novel mica inhibitor and preparation method and use method thereof Download PDFInfo
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- CN101850305A CN101850305A CN 201010201672 CN201010201672A CN101850305A CN 101850305 A CN101850305 A CN 101850305A CN 201010201672 CN201010201672 CN 201010201672 CN 201010201672 A CN201010201672 A CN 201010201672A CN 101850305 A CN101850305 A CN 101850305A
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Abstract
The invention discloses a novel mica inhibitor and a preparation method and a use method thereof. The mica inhibitor is N-methyl-9-heptadecenoic amidoethyl sodium sulfonate. The use method is as follows: (1) mica inhibitor N-methyl fatty amido acetate is prepared into aqueous solution with 5 to 10 percent of weight concentration; (2) mica ore is crushed or ground into 0.1mm to 2mm; (3) each ton of ore is added with 100g to 500g of mica inhibitor and 100g to 800g of carboxylic acid collector and uniformly mixed for 5 to 10 minutes, and deferrization operation is carried out before mica floatation. In the deferrization operation before mica floatation, the mica inhibitor is added to inhibit mica from floating up, so that the loss rate of mica is reduced. The mica recovery efficiency is increased. The mica inhibitor solves the problem that the loss rate of mica is high in the deferrization operation of floatation before mica floatation operation, the ferric mineral adsorbed on the surface of mica can be separated from the surface of mica, and during the floatation of ferric mineral, less mica is mechanically entrapped to float up.
Description
Technical field
The present invention relates to a kind of novel mica inhibiting agent and preparation method thereof and using method.
Background technology
Mica concentrate product has certain limitation to iron mineral content, and is in order to reduce iron mineral content in the mica concentrate product, generally floating except that iron mineral with the carboxylic acids collecting agent earlier before the mica flotation.
But in floatation process, because mica surface regional area elecrtonegativity is very high, and therefore many iron minerals surface lotus positive electricity or be neutral be easy to be adsorbed on mica surface, causes floatingly during except that iron mineral, and mica is carried come-up secretly, loses bigger.
As suppressing mica, then cause the back mica flotation operation rate of recovery to decline to a great extent with inhibitor such as silicate.
Summary of the invention
The technical issues that need to address of the present invention just are to overcome the defective of prior art, a kind of novel mica inhibiting agent and preparation method thereof and using method are provided, mica inhibiting agent of the present invention is added in deferrization operation before the mica flotation, suppresses the mica come-up, reduces the mica loss late.Improve the mica organic efficiency.It has solved the big problem of flotation deferrization operation mica loss late before the mica flotation operation, can make the iron mineral that is adsorbed on mica surface break away from mica surface, and mica can the mechanical entrapment come-up when floating except that iron mineral.
For addressing the above problem, the present invention adopts following technical scheme:
A kind of novel mica inhibiting agent of the present invention, described mica inhibiting agent are N methyl 90 seven alkene amido-ethyl sodium sulfonates; Its molecular formula is:
The present invention discloses a kind of preparation method of novel mica inhibiting agent, described step is:
The first step: generate ethylenehydrinsulfonic acid sodium with sodium hydrogensulfite and oxirane under the condition of heating, chemical reaction is as shown in the formula (1);
Second step: generate N-methyltaurine sodium with methylamine and ethylenehydrinsulfonic acid sodium under the condition of pressurization of heating, chemical reaction is as shown in the formula (2);
The 3rd step: carry out condensation reaction with oleoyl chloride and N-methyltaurine sodium and generate N methyl 90 seven alkene amido-ethyl sodium sulfonates, chemical reaction is as shown in the formula (3);
The present invention discloses a kind of using method of described novel mica inhibiting agent, comprise the following steps:
(1) outfit of the mica inhibiting agent aqueous solution: it is 5~10% the aqueous solution that mica inhibiting agent N methyl 90 seven alkene amido-ethyl sodium sulfonates are made into weight concentration;
(2) ore treatment: with mica ore reduction or ore grinding to 0.1-2mm;
(3) the deferrization operation before the mica flotation: the mica inhibiting agent aqueous solution by step (1) preparation that ore per ton adds 100-500g fully stirred 5-10 minute, the carboxylic acids collecting agent that adds 100-800g more fully stirred 5-10 minute, carried out the preceding deferrization operation of mica flotation.
Described mica ore is micaceous raw ore.
The present invention is applicable to the mine of some production mica concentrate, and mica inhibiting agent of the present invention is added in the deferrization operation before the mica flotation, suppresses the mica come-up, reduces the mica loss late.Improve the mica organic efficiency.
The specific embodiment
The preparation of embodiment 1 mica inhibiting agent
The first step: generate ethylenehydrinsulfonic acid sodium with sodium hydrogensulfite and oxirane under the condition of heating, chemical reaction is as shown in the formula (1);
Second step: generate N-methyltaurine sodium with methylamine and ethylenehydrinsulfonic acid sodium under the condition of pressurization of heating, chemical reaction is as shown in the formula (2);
The 3rd step: carry out condensation reaction with oleoyl chloride and N-methyltaurine sodium and generate N methyl 90 seven alkene amido-ethyl sodium sulfonates, chemical reaction is as shown in the formula (3);
The using method of embodiment 2 novel mica inhibiting agents
(1) outfit of the mica inhibiting agent aqueous solution: it is 5% the aqueous solution that mica inhibiting agent N methyl 90 seven alkene amido-ethyl sodium sulfonates are made into weight concentration;
(2) ore treatment: with the ore reduction of mica concentrate or ore grinding to 1mm;
(3) the deferrization operation before the mica flotation: the mica inhibiting agent aqueous solution by step (1) preparation that ore per ton adds 100g fully stirred 10 minutes, and the carboxylic acids collecting agent that adds 100g more fully stirred 10 minutes, carried out the preceding deferrization operation of mica flotation.
Embodiment 3
(1) outfit of the mica inhibiting agent aqueous solution: it is 10% the aqueous solution that mica inhibiting agent N methyl 90 seven alkene amido-ethyl sodium sulfonates are made into weight concentration;
(2) ore treatment: with micaceous raw ore ore reduction or ore grinding to less than 2mm;
(3) the deferrization operation before the mica flotation: the mica inhibiting agent aqueous solution by step (1) preparation that ore per ton adds 500g fully stirred 5 minutes, and the carboxylic acids collecting agent that adds 800g more fully stirred 5~10 minutes, carried out the preceding deferrization operation of mica flotation.
The present invention is applicable to the mine that produces the mica concentrate, and mica inhibiting agent of the present invention is added in the deferrization operation before the mica flotation, suppresses the mica come-up, reduces the mica loss late.Improve the mica organic efficiency.
It should be noted that at last: obviously, the foregoing description only is for example of the present invention clearly is described, and is not the qualification to embodiment.For those of ordinary skill in the field, can also make other changes in different forms on the basis of the above description.Here need not also can't give exhaustive to all embodiments.And conspicuous variation of being extended out thus or change still are among protection scope of the present invention.
Claims (4)
2. the preparation method of novel mica inhibiting agent as claimed in claim 1, it is characterized in that: described step is:
The first step: generate ethylenehydrinsulfonic acid sodium with sodium hydrogensulfite and oxirane under the condition of heating, chemical reaction is as shown in the formula (1);
Second step: generate N-methyltaurine sodium with methylamine and ethylenehydrinsulfonic acid sodium under the condition of pressurization of heating, chemical reaction is as shown in the formula (2);
The 3rd step: carry out condensation reaction with oleoyl chloride and N-methyltaurine sodium and generate N methyl 90 seven alkene amido-ethyl sodium sulfonates, chemical reaction is as shown in the formula (3);
3. the using method of novel mica inhibiting agent as claimed in claim 1, it is characterized in that: described using method comprises the following steps:
(1) outfit of the mica inhibiting agent aqueous solution: it is 5~10% the aqueous solution that mica inhibiting agent N methyl 90 seven alkene amido-ethyl sodium sulfonates are made into weight concentration;
(2) ore treatment: with mica ore reduction or ore grinding to 0.1-2mm;
(3) the deferrization operation before the mica flotation: the mica inhibiting agent by step (1) preparation that ore per ton adds 100-500g fully stirred 5-10 minute, the carboxylic acids collecting agent that adds 100-800g more fully stirred 5-10 minute, carried out the preceding deferrization operation of mica flotation.
4. the using method of novel mica inhibiting agent as claimed in claim 3, it is characterized in that: described mica ore is micaceous raw ore.
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CN2010102016720A CN101850305B (en) | 2010-06-17 | 2010-06-17 | Novel mica inhibitor and preparation method and use method thereof |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102489408A (en) * | 2011-12-19 | 2012-06-13 | 湖南有色金属研究院 | Flotation method for separating copper form mica |
CN103084274A (en) * | 2013-01-25 | 2013-05-08 | 湖南有色金属研究院 | Preparation method of high grade copper oxide concentrate |
CN110903222A (en) * | 2019-12-16 | 2020-03-24 | 万华化学集团股份有限公司 | Preparation method of N-methyl sodium taurate |
CN111004156A (en) * | 2019-12-23 | 2020-04-14 | 张家港格瑞特化学有限公司 | Method for synthesizing fatty acyl amino acid surfactant by direct method |
CN111072525A (en) * | 2019-12-26 | 2020-04-28 | 万华化学集团股份有限公司 | Preparation method of N-methyl sodium taurate |
CN111269151A (en) * | 2020-03-03 | 2020-06-12 | 万华化学集团股份有限公司 | Method for preparing taurine from sodium isethionate |
CN111689880A (en) * | 2020-07-13 | 2020-09-22 | 万华化学集团股份有限公司 | Method for preparing taurine from sodium isethionate |
Citations (1)
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CN101185916A (en) * | 2007-12-12 | 2008-05-28 | 吉林大学 | Method for recovering specular stone from debris containing specular stone |
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2010
- 2010-06-17 CN CN2010102016720A patent/CN101850305B/en active Active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101185916A (en) * | 2007-12-12 | 2008-05-28 | 吉林大学 | Method for recovering specular stone from debris containing specular stone |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102489408B (en) * | 2011-12-19 | 2013-04-10 | 湖南有色金属研究院 | Flotation method for separating copper form mica |
CN102489408A (en) * | 2011-12-19 | 2012-06-13 | 湖南有色金属研究院 | Flotation method for separating copper form mica |
CN103084274A (en) * | 2013-01-25 | 2013-05-08 | 湖南有色金属研究院 | Preparation method of high grade copper oxide concentrate |
CN103084274B (en) * | 2013-01-25 | 2014-06-11 | 湖南有色金属研究院 | Preparation method of high grade copper oxide concentrate |
CN110903222B (en) * | 2019-12-16 | 2022-02-18 | 万华化学集团股份有限公司 | Preparation method of N-methyl sodium taurate |
CN110903222A (en) * | 2019-12-16 | 2020-03-24 | 万华化学集团股份有限公司 | Preparation method of N-methyl sodium taurate |
CN111004156A (en) * | 2019-12-23 | 2020-04-14 | 张家港格瑞特化学有限公司 | Method for synthesizing fatty acyl amino acid surfactant by direct method |
CN111072525A (en) * | 2019-12-26 | 2020-04-28 | 万华化学集团股份有限公司 | Preparation method of N-methyl sodium taurate |
CN111072525B (en) * | 2019-12-26 | 2022-02-15 | 万华化学集团股份有限公司 | Preparation method of N-methyl sodium taurate |
CN111269151A (en) * | 2020-03-03 | 2020-06-12 | 万华化学集团股份有限公司 | Method for preparing taurine from sodium isethionate |
CN111269151B (en) * | 2020-03-03 | 2022-03-11 | 万华化学集团股份有限公司 | Method for preparing taurine from sodium isethionate |
CN111689880A (en) * | 2020-07-13 | 2020-09-22 | 万华化学集团股份有限公司 | Method for preparing taurine from sodium isethionate |
CN111689880B (en) * | 2020-07-13 | 2022-03-11 | 万华化学集团股份有限公司 | Method for preparing taurine from sodium isethionate |
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