CN113117882B - Pre-flotation method for low-grade phosphorite in high sesquioxide - Google Patents

Pre-flotation method for low-grade phosphorite in high sesquioxide Download PDF

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CN113117882B
CN113117882B CN201911390506.7A CN201911390506A CN113117882B CN 113117882 B CN113117882 B CN 113117882B CN 201911390506 A CN201911390506 A CN 201911390506A CN 113117882 B CN113117882 B CN 113117882B
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flotation
phosphorite
sesquioxide
concentrate
grade
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CN113117882A (en
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徐政
黄孝振
王国伟
纪仲光
张明江
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GRINM Resources and Environment Technology Co Ltd
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    • 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
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Abstract

The invention provides a pre-flotation method for low-grade phosphorite in high sesquioxide. By the pre-flotation treatment process, apatite and siliceous gangue minerals can be effectively separated, the grade and recovery rate index of phosphate concentrate are improved, and the method is one of the methods for realizing the efficient utilization of phosphate rock resources. The process flow comprises the following steps: controlling the grinding fineness of the phosphorite to be 60 to 85 percent of 200 meshes; adjusting the concentration of the ore pulp to be between 25 and 35 percent, firstly carrying out primary prefloat before formal flotation separation, taking products of the prefloat as tailings, and then carrying out primary coarse flotation and secondary fine flotation to obtain final concentrate P 2 O 5 The grade reaches 32.5 to 35.5 percent, and the recovery rate is 80 to 90 percent. The process disclosed by the invention can realize efficient and short-flow flotation of the low-grade phosphorite in the high sesquioxide, improves the comprehensive index of phosphorite sorting, and is low in medicament consumption, high in flotation efficiency, energy-saving and environment-friendly.

Description

Pre-flotation method for low-grade phosphorite in high sesquioxide
Technical Field
The invention belongs to the technical field of mineral processing engineering, relates to a phosphorite pre-flotation method, and particularly relates to a high-sesquioxide medium-low grade phosphorite pre-flotation method.
Background
Phosphorite is an important strategic resource in China, is an important chemical mineral raw material for preparing phosphate fertilizer, producing yellow phosphorus, phosphoric acid and other various phosphorus products, is an important mineral for guaranteeing food safety, is a material basis of fine phosphorus chemical industry, and has important position and function in national economy. According to 2016 mineral resource reports in China, the total resource amount of 231.1 million tons of phosphorite resources is only second to Morocco by 2015 and is located at the 2 nd position in the world. However, the ore mainly comprises medium-low grade sedimentary phosphate rock (collophanite), the rich ore resource is less, the difficulty of mining and selecting is greater, and the phosphorite as a non-renewable resource becomes one of important strategic resources in China.
In the process of mineral separation of phosphorite, the current dominant mineral separation methods include flotation, scrubbing and desliming, roasting-digestion, heavy medium mineral separation, combined mineral separation process, chemical mineral separation, microbial treatment and the like. The flotation process has stronger adaptability compared with other separation methods, and particularly when the phosphorus ore and the gangue are closely symbiotic and have low content, only the flotation method can obtain better separation effect. Most phosphorite resources in China are treated by a flotation method.
The phosphate ore contains more potassium feldspar, sodium feldspar, quartz and dolomite, has low grade and high content of sesquioxide, and directly influences the subsequent preparation quality and preparation process of the phosphoric acid. The efficient flotation of the phosphorite is realized by adopting the flotation treatment process, so that the concentrate grade is improved, the recovery rate is increased, the content of sesquioxide is reduced, and the efficient flotation process plays an important role in the subsequent phosphoric acid production process. Therefore, the exploration of the efficient flotation separation process plays an important role in fully utilizing phosphorite resources and improving the production quality of phosphoric acid.
Disclosure of Invention
In order to solve the problems, the invention aims to provide a pre-flotation method for low-grade and medium-grade phosphorite of high sesquioxide, which has the advantages of good process stability, high flotation efficiency, short flotation flow and low medicament consumption, and meets the requirements of an energy-saving, environment-friendly and clean siliceous phosphorite beneficiation process.
In order to achieve the aim, the invention provides a pre-flotation method for low-grade phosphorite in high sesquioxide, which comprises the following steps:
(1) Grinding the low-grade phosphorite in the high sesquioxide to the content of 60-85% of 200 meshes, adding water to prepare ore pulp, and adjusting the concentration of the ore pulp to 23-30%; controlling the temperature of ore pulp at 20-35 ℃;
(2) Adding a mixed reagent into the ore pulp, mixing for 4min, and then performing pre-flotation for 3min to obtain tailings 1 and pre-flotation concentrate;
(3) Adding the pre-flotation concentrate into a mixed reagent, mixing for 4min, and then performing rough concentration for 4min to obtain tailings 2 and rough concentrate;
(4) Carrying out concentration I on the rough concentration concentrate, wherein the time for the concentration I is 3min, and obtaining middling 1 and concentrate I;
(5) And (3) carrying out concentration II on the concentrate I, wherein the concentration II lasts for 3min, and obtaining middling 2 and concentrate.
Preferably, P in the high sesquioxide middle and low grade phosphorite 2 O 5 2.5-26.0 percent of the total content of the sesquioxide, 4-8 percent of the total content of the sesquioxide and 0.6-4.0 percent of the total content of the MgO.
Preferably, in the step (3), the adding amount of the mixed reagent added in the phosphorite roughing is 300.0 g/t-2.7 kg/t.
The ratio of the regulator to the collector is 1.
Preferably, in the step (2), the amount of the mixed reagent added in the pre-flotation is 1.0-50.0% of the amount of the crude reagent.
The flotation method provided by the invention is characterized in that the pre-flotation is firstly carried out on the selected raw ore, the concentrate subjected to the pre-flotation is subjected to the process flow of once roughing and twice fine concentration, and no flotation agent is added in the fine concentration process.
After the process flow is selected, P 2 O 5 The content reaches 32.5-35.5%, the recovery rate is 80-90%, and the sesquioxide is reduced to one half to one fourth of the original ore.
The invention has the beneficial effects that:
the invention provides a pre-flotation method for middle-low grade phosphorite of high sesquioxide, which is characterized in that a small amount of flotation reagent is added for pre-flotation before phosphorite ore is subjected to normal flotation, the product obtained by flotation is used as tailings, and then a coarse flotation process and a fine flotation process are performed.
The method can effectively treat the low-grade siliceous phosphorite in the high sesquioxide.
2 the invention can effectively reduce the content of sesquioxide and improve the quality of phosphate concentrate by adopting a pre-flotation method.
3, after the pre-flotation treatment is adopted, the flotation process can be shortened, the ore dressing efficiency is improved, and the method is one of new processes for treating the low-grade and medium-grade phosphorite of the high sesquioxide by flotation.
Drawings
FIG. 1 is a process flow diagram of the flotation method provided by the invention
Figure 2 is a flow diagram of a process without the use of pre-flotation.
Figure 3 is a flow chart of a process employing pre-flotation.
Figure 4 is a flow diagram of a process without the use of pre-flotation.
Figure 5 is a flow chart of a process employing pre-flotation.
Detailed Description
The present invention is further illustrated by the following examples, but the embodiments of the present invention are not limited thereto.
The mixed drug used in the examples of the present invention is a mixture of a regulator and the collecting agents are purchased from the science and technology corporation of the Xiangxiang mining of filial piety, the modifier product model is CJ102 and the collector product model is G16.
The invention provides a pre-flotation method for low-grade phosphorite in high sesquioxide, which comprises the following steps as shown in figure 1:
(1) Grinding the low-grade phosphorite in the high sesquioxide to the content of 60-85% of 200 meshes, adding water to prepare ore pulp, and adjusting the concentration of the ore pulp to 23-30%; controlling the temperature of ore pulp at 20-35 ℃;
(2) Adding a mixed reagent into the ore pulp, mixing for 4min, and then performing pre-flotation for 3min to obtain tailings 1 and pre-flotation concentrate (rough flotation feed);
(3) Adding the pre-flotation concentrate (rough concentration feed) into a mixed reagent, mixing for 4min, and then performing rough concentration for 4min to obtain tailings 2 and rough concentration concentrate (fine concentration I feed);
(4) Subjecting the rough concentrate (I feed for refining) to I concentration for 3min to obtain middling 1 and I concentrate (II feed for refining)
(5) And (4) carrying out concentration II on the concentrate I (fed material of the concentration II), wherein the time of the concentration II is 3min, and obtaining middling 2 and concentrate.
Wherein P in the high sesquioxide middle-low grade phosphorite 2 O 5 2.5-26.0 percent of the total content of the sesquioxide, 4-8 percent of the total content of the sesquioxide and 0.6-4.0 percent of the total content of the MgO.
In the step (3), the adding amount of the mixed reagent added in the rough concentration of the phosphorite is 300.0 g/t-2.7 kg/t.
In the step (2), the amount of the mixed reagent added in the pre-flotation is 1.0-50.0% of the amount of the crude reagent.
Example 1
In the mixed reagent used for the low-grade phosphorite in a certain high sesquioxide, the mass ratio of a regulator CJ102 to a collector G16 is 1. The flow without pre-flotation is shown in figure 2, the flotation results are shown in table 1, the flow with pre-flotation is shown in figure 3, the flow with pre-flotation is 500g/t, the coarse flotation is 1100g/t, and the flotation results are shown in table 2.
TABLE 1 test results without pre-flotation
Figure BDA0002344784540000041
TABLE 2 results of the pre-flotation test
Figure BDA0002344784540000042
As can be seen from the test results in tables 1 and 2, the grade of the phosphate concentrate is improved by 1.5% under the condition that the recovery rate is not greatly different by adopting the process flow of pre-flotation rather than pre-flotation; in addition, although the total yield of the tailings in the pre-flotation process is large, the total grade is reduced by 1 percent. Proves that the adoption of the pre-flotation process flow is beneficial to the separation of apatite and gangue minerals in siliceous phosphorite.
Example 2
In the mixed reagent used for the low-grade phosphorite in a certain high sesquioxide, the mass ratio of the regulator CJ102 to the collector G16 is 1. The flow without using the pre-flotation is shown in FIG. 4, the dosage of the mixed rougher flotation agent is 1800g/t, and the flotation results are shown in Table 3, while the flow with the pre-flotation is shown in FIG. 5, comparing the dosage of the mixed rougher flotation agent with 390g/t, and the dosage of the rougher flotation agent with 1400g/t, and the flotation results are shown in Table 4.
TABLE 3 test results without pre-flotation
Figure BDA0002344784540000043
TABLE 4 results of the pre-flotation test
Figure BDA0002344784540000051
As can be seen from the test results in tables 3 and 4, the process flow of pre-flotation rather than pre-flotation is adopted, the grade of the phosphate concentrate is improved by about 2.5%, and the recovery rate is improved by 6%; meanwhile, the total yield and grade of the tailings obtained by adopting the pre-flotation process are reduced. The method proves that the pre-flotation process is firstly adopted, so that the separation of apatite and gangue minerals in siliceous phosphorite is facilitated, and the separation effect of the low-grade phosphorite in the high sesquioxide is improved.
In conclusion, the novel pre-flotation process disclosed by the invention shortens the subsequent conventional flotation process, improves the efficiency of phosphorite flotation and finally obtains the concentrate P 2 O 5 The grade reaches 32.5 to 35.5 percent, the recovery rate reaches 80 to 90 percent, the continuous and stable production can be realized, and the comprehensive index of the low-grade phosphorite in the high sesquioxide is improved. The pretreatment process can improve the grade of the phosphorite, reduce the content of the sesquioxide, has short flow and high efficiency, and is one of the methods for improving the utilization rate of the phosphorus resources.
Although the present invention has been described above, the present invention is not limited to the above-mentioned embodiments, which are only illustrative and not restrictive, and those skilled in the art can make many modifications without departing from the spirit of the present invention, which falls within the protection of the present invention.

Claims (1)

1. The pre-flotation method for the low-grade phosphorite in the high sesquioxide is characterized by comprising the following steps of:
(1) Grinding the low-grade phosphorite in the high sesquioxide to the content of 60-85% of 200 meshes, adding water to prepare ore pulp, and adjusting the concentration of the ore pulp to 23-30%; controlling the temperature of ore pulp at 20-35 ℃;
(2) Adding a mixed reagent into the ore pulp, mixing for 4min, then carrying out pre-flotation for 3min, and taking a product obtained by flotation as tailings I to obtain tailings 1 and pre-flotation concentrate;
(3) Adding the pre-flotation concentrate into a mixed reagent, mixing for 4min, and then roughing for 4min to obtain tailings 2 and roughed concentrate;
(4) Carrying out concentration I on the rough concentration concentrate, wherein the time for the concentration I is 3min, and obtaining middling 1 and concentrate I;
(5) Carrying out concentration II on the concentrate of the concentration I, wherein the time for the concentration II is 3min, and obtaining middling 2 and concentrate;
wherein P in the high sesquioxide middle-low grade phosphorite 2 O 5 2.5-26.0 percent of the total content of the sesquioxide, 4-8 percent of the total content of the sesquioxide and 0.6-4.0 percent of the total content of the MgO;
the mixed reagent is a mixture of a regulator CJ102 and a collector G16, wherein the mass ratio of the regulator CJ102 to the collector G16 is 1;
in the step (3), the adding amount of the mixed reagent added in the rough concentration of the phosphorite is 300.0 g/t-2.7 kg/t;
in the step (2), the amount of the mixed reagent added in the pre-flotation process is 1.0% -50.0% of the amount of the crude reagent.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4904375A (en) * 1986-05-16 1990-02-27 Imc Fertilizer, Inc. Sodium silicate as a phosphate flotation modifier
CN107497606A (en) * 2017-09-13 2017-12-22 化工部长沙设计研究院 A kind of regime of agent of phosphorus ore direct flotation roughing
CN109954579A (en) * 2019-03-29 2019-07-02 中冶北方(大连)工程技术有限公司 Two product ore-dressing technique of apatite ilmenite
CN110293006A (en) * 2019-07-19 2019-10-01 宜都兴发化工有限公司 The beneficiation method of sesquichloride in a kind of reduction collophane

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4904375A (en) * 1986-05-16 1990-02-27 Imc Fertilizer, Inc. Sodium silicate as a phosphate flotation modifier
CN107497606A (en) * 2017-09-13 2017-12-22 化工部长沙设计研究院 A kind of regime of agent of phosphorus ore direct flotation roughing
CN109954579A (en) * 2019-03-29 2019-07-02 中冶北方(大连)工程技术有限公司 Two product ore-dressing technique of apatite ilmenite
CN110293006A (en) * 2019-07-19 2019-10-01 宜都兴发化工有限公司 The beneficiation method of sesquichloride in a kind of reduction collophane

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
我国沉积型条带状磷块岩分布特点及选矿技术;袁俊宏等;《武汉工程大学学报》;20110228;第33卷(第02期);第68-71页 *
新浦磷矿浮选药剂及常温浮选研究;纪丽凡;《化工矿物与加工》;20000731(第07期);第9-10页 *
贵州某硅钙质磷矿岩的浮选试验研究;曾理等;《矿产保护与利用》;20111231(第5-6期);第79-82页 *

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