CN113171761A - Porous electrostatic spraying microsphere for treating antimony-containing wastewater and preparation method thereof - Google Patents

Porous electrostatic spraying microsphere for treating antimony-containing wastewater and preparation method thereof Download PDF

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CN113171761A
CN113171761A CN202110453743.4A CN202110453743A CN113171761A CN 113171761 A CN113171761 A CN 113171761A CN 202110453743 A CN202110453743 A CN 202110453743A CN 113171761 A CN113171761 A CN 113171761A
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electrostatic spraying
microspheres
antimony
porous
containing wastewater
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CN113171761B (en
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涂凌波
黄文财
代焕芳
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Fujian Environmental Protection Design Institute Co ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26Synthetic macromolecular compounds
    • B01J20/265Synthetic macromolecular compounds modified or post-treated polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28014Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
    • B01J20/28016Particle form
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/28Treatment of water, waste water, or sewage by sorption
    • C02F1/285Treatment of water, waste water, or sewage by sorption using synthetic organic sorbents
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/10Inorganic compounds
    • C02F2101/20Heavy metals or heavy metal compounds

Abstract

The invention discloses a preparation method of porous electrostatic spray microspheres for treating antimony-containing wastewater, which specifically comprises the following steps: (1) dissolving polyacrylonitrile and polyvinylpyrrolidone powder in an N, N-dimethylformamide solvent, and stirring at 50-60 ℃ for 2.0-12.0 h to form a uniform electrostatic spraying solution; (2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper; (3) putting the atomized microsphere precursor obtained in the step (2) into distilled water for washing and carrying out ultrasonic treatment; (4) mixing the washed and ultrasonically treated atomized microsphere precursor with hydroxylamine hydrochloride, anhydrous sodium carbonate and distilled water, stirring, and carrying out in-situ amidoximation reaction to obtain electrostatic spraying microspheres; (5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed products in an oven, and then carrying out vacuum dehydration on the dried products to finally obtain the porous electrostatic spraying microspheres.

Description

Porous electrostatic spraying microsphere for treating antimony-containing wastewater and preparation method thereof
Technical Field
The invention belongs to the technical field of preparation of fixed body adsorbents and materials, and particularly relates to a porous electrostatic spray microsphere for treating antimony-containing wastewater and a preparation method thereof.
Background
After the biochemical treatment, the printing and dyeing wastewater still contains a large amount of heavy metal substances, and the pollutants are represented by antimony. In recent years, the content of antimony in printing and dyeing wastewater is seriously exceeded, and the concentration of antimony before treatment can be as high as ten thousand mu g/L. The excessive antimony concentration is proved to have teratogenic and carcinogenic effects on human bodies, and seriously threatens the life and health of local people in the printing and dyeing industry. The reported news shows that the excessive antimony concentration in the printing and dyeing wastewater causes the production stoppage and the rectification of many printing and dyeing enterprises, and huge economic loss is caused. Studies show that antimony in the printing and dyeing wastewater mainly exists in the form of pentavalent acid radicals (Sb (V)), and the chemical structure of the nonmetal cations brings difficulty for antimony treatment. Therefore, the antimony for scientifically and effectively treating the printing and dyeing wastewater becomes a problem to be solved urgently.
At present, there are many methods for removing antimony pollutants in printing and dyeing wastewater, and the most studied and used methods mainly comprise an adsorption method, a precipitation method and an electrochemical method. Among them, the adsorption method is widely used because of its advantages such as high efficiency, economy, and easy operation. The traditional antimony removal adsorbent mostly adopts inorganic adsorbents such as biomass, metal oxides, ores and the like, the maximum adsorption capacity of the traditional antimony removal adsorbent is generally 20mg/g, and the adsorption capacity is limited because the natural inorganic adsorbents lack a pore channel structure and have insufficient adsorption power; the other type of antimony removal adsorbent is carbon material adsorbents such as activated carbon, carbon nanotubes and graphene, the maximum adsorption capacity of the adsorbent to antimony is generally not more than 80mg/g, and the main reason for limiting the adsorption capacity is that the adsorbent lacks active functional groups as adsorption sites and cannot effectively capture antimony ions. Therefore, there is an important research value in developing an organic adsorbent having a high adsorption capacity.
The organic resin for water treatment has a large number of active functional groups (amino groups, carboxyl groups, sulfenyl groups, oximino groups and the like), is commonly used for adsorbing heavy metal pollutants Pb, Hg, Cu and the like, has good adsorption capacity and has wide application prospect. Chinese patent with publication number CN108794661A discloses an amidoximated polyacrylonitrile and a preparation method and application thereof, wherein the amidoximated polyacrylonitrile material prepared by mixing polyacrylonitrile, hydroxylamine material and salt material for reaction can be used as an adsorbent, the amidoximated polyacrylonitrile material has a porous structure, the pore size distribution is from nanometer to micrometer, and the amidoximated polyacrylonitrile material has chelating adsorption and physical adsorption capacity and can be used for treating heavy metal wastewater; chinese patent with publication number CN109364891A discloses a modified polyacrylonitrile for treating antimony-containing wastewater and a preparation method thereof, wherein the modified polyacrylonitrile particle adsorbent prepared by in-situ amidoximation of a polyacrylonitrile substrate is specifically disclosed and used for removing antimony in wastewater, the adsorption capacity of the modified polyacrylonitrile particle adsorbent is 90-160 mg/g, but the modified polyacrylonitrile particle adsorbent prepared by the method lacks a pore channel structure, and the maximum adsorption capacity for removing antimony is only 160 mg/g. Therefore, increasing the pore structure inside the adsorbent and increasing the adsorption power are one of the ways to improve the adsorption capacity of the adsorbent to antimony.
Disclosure of Invention
In order to solve the problem that an antimony removal adsorbent in the prior art is short of a pore channel structure, the invention provides a porous electrostatic spraying microsphere for treating antimony-containing wastewater and a preparation method thereof.
The technical scheme of the invention is as follows:
the invention discloses a preparation method of porous electrostatic spraying microspheres for treating antimony-containing wastewater, which specifically comprises the following steps:
(1) dissolving polyacrylonitrile and polyvinylpyrrolidone in an N, N-dimethylformamide solvent, and stirring at 50-60 ℃ for 2.0-12.0 h to form a uniform electrostatic spraying solution;
(2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper;
(3) putting the atomized microsphere precursor obtained in the step (2) into distilled water for washing and carrying out ultrasonic treatment;
(4) adding the washed and ultrasonically treated atomized microsphere precursor, hydroxylamine hydrochloride and anhydrous sodium carbonate into distilled water, mixing, stirring, and carrying out in-situ amidoximation reaction to obtain electrostatic spraying microspheres;
(5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed products in an oven, and then carrying out vacuum dehydration on the dried products to finally obtain the porous electrostatic spraying microspheres.
Further, in the step (1), the mass ratio of polyacrylonitrile to polyvinylpyrrolidone is 0.2-5.0: 1, and the mass percentage of the polymer base material of polyacrylonitrile and polyvinylpyrrolidone in the solvent N, N-dimethylformamide is 0.1-2.5 wt%.
Further, the voltage of electrostatic spraying in the step (2) is 10.0-30.0V, the pushing speed is 0.1-5.0 mL/h, and the distance for collecting the precursor of the atomized microspheres by the roller is 0.1-0.8 m.
Further, the ultrasonic treatment time in the step (3) is 10.0-60.0 min.
Further, the mass ratio of the atomized microsphere precursor, hydroxylamine hydrochloride and anhydrous sodium carbonate added in the amidoximation reaction in the step (4) is 0.1-5.0: 6: 5.8; the volume ratio of the total mass of the atomized microsphere precursor, the hydroxylamine hydrochloride and the anhydrous sodium carbonate to the distilled water is 11.9-16.8 g:100 mL.
Further, the heating temperature of the water bath for the amidoxime reaction is 60-80 ℃.
Further, the microsphere product washed in the step (5) is dried in an oven at 50-60 ℃ for 2-4 h, and then dried in a vacuum atmosphere at 60-70 ℃ for 12-48 h.
The invention also provides the porous electrostatic spraying microsphere prepared by the preparation method for the porous electrostatic spraying microsphere for treating the antimony-containing wastewater, wherein the maximum adsorption capacity of the porous electrostatic spraying microsphere is 300.0-400.0 mg/g.
The invention also provides application of the porous electrostatic spraying microspheres for treating the antimony-containing wastewater in the antimony-containing wastewater.
Compared with the prior art, the invention has the beneficial effects that:
(1) the porous electrostatic spraying microspheres are prepared by taking polyacrylonitrile and polyvinylpyrrolidone as raw materials, utilizing electrostatic spraying to generate a large number of fine pore channel structures on the formed microspheres in a high-voltage mode, and controlling the spraying process conditions to obtain the electrostatic spraying porous microspheres with proper pore channel structures; meanwhile, in combination with the in-situ amidoximation reaction, the in-situ amidoximation reaction not only has a pore-forming effect, but also enables the porous electrostatic spraying microsphere to have chelating adsorption and physical adsorption capacities at the same time, has good ion selectivity and adsorption power, and improves the adsorption performance.
(2) The polyacrylonitrile and the polyvinylpyrrolidone used in the invention have rich raw material sources, are traditional chemical raw materials, have simple preparation method and low energy consumption, and are suitable for industrial production.
(3) The porous electrostatic spray microsphere prepared by the invention has the advantages of high adsorption speed, large maximum adsorption capacity, good desorption effect and repeated recycling.
Drawings
FIG. 1 is a scanning electron micrograph of porous electrostatically sprayed microspheres made according to example 1 of the present invention;
FIG. 2 is a graph showing the adsorption kinetics of porous electrostatically-sprayed microspheres prepared according to example 1 of the present invention for adsorbing antimony ions in wastewater, wherein qt is the adsorption capacity; t-adsorption time.
Detailed Description
In order to facilitate understanding of the present invention, the technical solutions of the present invention will be further described with reference to the following detailed description and the accompanying drawings, but the present invention is not limited thereto.
Example 1
A preparation method of porous electrostatic spraying microspheres for treating antimony-containing wastewater specifically comprises the following steps:
(1) dissolving 1g of polyacrylonitrile and 1g of polyvinylpyrrolidone (1:1) in 100mL of N, N-dimethylformamide solvent, wherein the mass percentage of the polymer base materials of the polyacrylonitrile and the polyvinylpyrrolidone in the solvent N, N-dimethylformamide is 2 wt%, and stirring at 50 ℃ for 2.0h to obtain uniform electrostatic spraying solution;
(2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper; wherein the voltage of electrostatic spraying is 20V, the injection speed is 0.1mL/h, and the distance for collecting the precursor of the atomized microspheres by the roller is 0.1 m;
(3) washing the mist microsphere precursor obtained in the step (2) in distilled water, and carrying out ultrasonic treatment for 10.0 min;
(4) adding 0.1g of washed and ultrasonically treated atomized microsphere precursor, 6.0g of hydroxylamine hydrochloride and 5.8g of anhydrous sodium carbonate into 100mL of distilled water, mixing, stirring, and carrying out in-situ amidoximation reaction at 60 ℃ to obtain electrostatic spraying microspheres;
(5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed product in a 50 ℃ drying oven for 2.0h, and dehydrating the dried product in a vacuum atmosphere at 70 ℃ for 12.0h to finally obtain the porous electrostatic spraying microspheres.
Example 2
A preparation method of porous electrostatic spraying microspheres for treating antimony-containing wastewater specifically comprises the following steps:
(1) dissolving 1g of polyacrylonitrile and 0.5g of polyvinylpyrrolidone (2:1) in 100mL of N, N-dimethylformamide solvent, wherein the mass percent of the polyacrylonitrile and polyvinylpyrrolidone polymer base material in the N, N-dimethylformamide solvent is 1.5 wt%, and stirring at 60 ℃ for 12.0h to obtain uniform electrostatic spraying solution;
(2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper; wherein the voltage of electrostatic spraying is 10.0V, the injection speed is 1.0mL/h, and the distance for collecting the precursor of the atomized microspheres by the roller is 0.4 m;
(3) washing the mist microsphere precursor obtained in the step (2) in distilled water, and carrying out ultrasonic treatment for 20.0 min;
(4) adding 5.0g of washed and ultrasonically treated atomized microsphere precursor, 6.0g of hydroxylamine hydrochloride and anhydrous sodium carbonate into distilled water, mixing, stirring, and carrying out in-situ amidoximation reaction at 70 ℃ to obtain electrostatic spraying microspheres;
(5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed product in a 60 ℃ drying oven for 4.0h, and dehydrating the dried product in a 60 ℃ vacuum atmosphere for 48.0h to finally obtain the porous electrostatic spraying microspheres.
Example 3
A preparation method of porous electrostatic spraying microspheres for treating antimony-containing wastewater specifically comprises the following steps:
(1) dissolving (5:1) 1g of polyacrylonitrile and 0.2g of polyvinylpyrrolidone in 40mL of N, N-dimethylformamide solvent, wherein the mass percent of the polyacrylonitrile and polyvinylpyrrolidone polymer base material in the N, N-dimethylformamide solvent is 2.5 wt%, and stirring at 55 ℃ for 10.0h to obtain uniform electrostatic spraying solution;
(2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper; wherein the voltage of electrostatic spraying is 30.0V, the injection speed is 5.0mL/h, and the distance for collecting the precursor of the atomized microspheres by the roller is 0.8 m;
(3) washing the mist microsphere precursor obtained in the step (2) in distilled water, and carrying out ultrasonic treatment for 60.0 min;
(4) adding 2.0g of the washed and ultrasonically treated atomized microsphere precursor, 6.0g of hydroxylamine hydrochloride and 5.8g of anhydrous sodium carbonate into 100mL of distilled water, mixing, stirring, and carrying out in-situ amidoximation reaction at 80 ℃ to obtain electrostatic spraying microspheres;
(5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed product in an oven at 55 ℃ for 3.0h, and removing the dried product in a vacuum atmosphere at 65 ℃ for 24.0h to finally obtain the porous electrostatic spraying microspheres.
Example 4
A preparation method of porous electrostatic spraying microspheres for treating antimony-containing wastewater specifically comprises the following steps:
(1) dissolving 0.1g of polyacrylonitrile and 0.5g of polyvinylpyrrolidone (0.2:1) in 600mL of N, N-dimethylformamide solvent, wherein the mass percent of the polymer base materials of the polyacrylonitrile and the polyvinylpyrrolidone in the solvent N, N-dimethylformamide is 0.1 wt%, and stirring at 50 ℃ for 8.0h to obtain uniform electrostatic spraying solution;
(2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper; wherein the voltage of electrostatic spraying is 20V, the injection speed is 2.0mL/h, and the distance for collecting the precursor of the atomized microspheres by the roller is 0.2 m;
(3) washing the mist microsphere precursor obtained in the step (2) in distilled water, and carrying out ultrasonic treatment for 10.0 min;
(4) adding 0.5g of washed and ultrasonically treated atomized microsphere precursor, 6.0g of hydroxylamine hydrochloride and 5.8g of anhydrous sodium carbonate into 100mL of distilled water, mixing, stirring, and carrying out in-situ amidoximation reaction at 60 ℃ to obtain electrostatic spraying microspheres;
(5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed product in a 50 ℃ drying oven for 2.0h, and dehydrating the dried product in a vacuum atmosphere at 70 ℃ for 20.0h to finally obtain the porous electrostatic spraying microspheres.
And (3) performance testing:
1. adsorption capacity test
In an adsorption experiment, 400mL of antimony-containing wastewater with the concentration of 50mg/L is prepared, then 0.1g of porous electrostatic spraying microsphere adsorbent is added, the mixture is put into a shaking table and is shaken at a constant speed at 25 ℃, sampling is carried out when the mixture is respectively 0.2, 0.5, 1.0, 1.5, 2.0, 3.0, 6.0 and 12.0 hours, the adsorption capacity is calculated after the concentration of antimony ions is measured, and the specific adsorption capacity is shown in Table 1:
TABLE 1 porous electrostatically sprayed microsphere adsorption capacities
Example 1 Example 2 Example 3 Example 4
Adsorption capacity (mg/g) 380 323 378 355
From the above table, the maximum adsorption capacity of the porous electrostatic spray microsphere prepared by the invention is 300.0-400.0 mg/g.
2. Referring to fig. 1, an SEM image of the porous electrostatic spray microspheres prepared according to example 1 of the present invention shows that the particle size of the porous electrostatic spray microspheres prepared according to the present invention is 0.2 to 0.75 μm.
3. Referring to fig. 2, an adsorption kinetics diagram of the porous electrostatic spray microspheres prepared according to example 1 of the present invention for adsorbing antimony ions in wastewater shows that an adsorption mechanism of the porous electrostatic spray microspheres for antimony in wastewater conforms to a quasi-second-order adsorption kinetics model, and the adsorption of the porous electrostatic spray microspheres for antimony in wastewater belongs to chemical adsorption, and relates to electron sharing or electron transfer between an adsorbent and an adsorbate.
The above description is only an embodiment of the present invention, and not intended to limit the scope of the present invention, and all modifications of equivalent structures and equivalent processes, which are made by the present specification, or directly or indirectly applied to other related technical fields, are included in the scope of the present invention.

Claims (10)

1. A preparation method of porous electrostatic spraying microspheres for treating antimony-containing wastewater is characterized by comprising the following steps:
(1) dissolving polyacrylonitrile and polyvinylpyrrolidone in an N, N-dimethylformamide solvent, and stirring at 50-60 ℃ for 2.0-12.0 h to form a uniform electrostatic spraying solution;
(2) placing the electrostatic spraying solution under electrostatic spraying equipment for electrostatic spraying, and collecting a vaporous microsphere precursor by adopting a roller wrapped by aluminum foil paper;
(3) putting the atomized microsphere precursor obtained in the step (2) into distilled water for washing and carrying out ultrasonic treatment;
(4) adding the washed and ultrasonically treated atomized microsphere precursor, hydroxylamine hydrochloride and anhydrous sodium carbonate into distilled water, mixing, stirring, and carrying out in-situ amidoximation reaction to obtain electrostatic spraying microspheres;
(5) and taking out the electrostatic spraying microspheres, soaking and washing the electrostatic spraying microspheres by using deionized water, drying the washed products in an oven, and then carrying out vacuum dehydration on the dried products to finally obtain the porous electrostatic spraying microspheres.
2. The method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to claim 1, wherein the method comprises the following steps: in the step (1), the mass ratio of polyacrylonitrile to polyvinylpyrrolidone is 0.2-5.0: 1, and the mass percentage of the polymer base material of polyacrylonitrile and polyvinylpyrrolidone in the solvent N, N-dimethylformamide is 0.1-2.5 wt%.
3. The method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to claim 1, wherein the method comprises the following steps: in the step (2), the voltage of electrostatic spraying is 10.0-30.0V, the injection speed is 0.1-5.0 mL/h, and the distance for collecting the precursor of the atomized microspheres by the roller is 0.1-0.8 m.
4. The method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to claim 1, wherein the method comprises the following steps: the ultrasonic treatment time in the step (3) is 10.0-60.0 min.
5. The method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to claim 1, wherein the method comprises the following steps: the mass ratio of the atomized microsphere precursor, hydroxylamine hydrochloride and anhydrous sodium carbonate added in the amidoximation reaction in the step (4) is 0.1-5.0: 6: 5.8; the volume ratio of the total mass of the atomized microsphere precursor, the hydroxylamine hydrochloride and the anhydrous sodium carbonate to the distilled water is 11.9-16.8 g:100 mL.
6. The method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to claim 1, wherein the method comprises the following steps: the water bath heating temperature of the amidoxime reaction is 60-80 ℃.
7. The method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to claim 1, wherein the method comprises the following steps: and (3) drying the microsphere product washed in the step (5) in a drying oven at 50-60 ℃ for 2-4 h, and then drying in a vacuum atmosphere at 60-70 ℃ for 12-48 h.
8. Porous electrostatic spraying microspheres obtained by the method for preparing porous electrostatic spraying microspheres for treating antimony-containing wastewater according to any one of claims 1 to 7.
9. The porous electrostatically-sprayed microspheres of claim 8 for treating wastewater containing antimony which are characterized by: the maximum adsorption capacity of the porous electrostatic spraying microspheres is 300.0-400.0 mg/g.
10. The use of the porous electrostatically-sprayed microspheres for treating antimony-containing wastewater as claimed in claim 8 in antimony-containing wastewater.
CN202110453743.4A 2021-04-26 2021-04-26 Porous electrostatic spraying microsphere for treating antimony-containing wastewater and preparation method thereof Active CN113171761B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116747715A (en) * 2023-04-14 2023-09-15 浙江大学 High-water flux nanofiltration membrane with gradient structure separation layer and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130168322A1 (en) * 2010-09-14 2013-07-04 Kaneka Corporation Amidoxime-modified polyacrylonitrile porous body
CN105924657A (en) * 2016-06-03 2016-09-07 广东工业大学 Preparation method of electrostatic spray nano microsphere with porous structure
CN107913677A (en) * 2017-12-12 2018-04-17 成都育芽科技有限公司 A kind of nanometer heavy metal wastewater thereby ionic adsorption microballoon and preparation method thereof
CN109364891A (en) * 2018-11-14 2019-02-22 上海交通大学 A kind of modified polyacrylonitrile and preparation method thereof handling stibium-containing wastewater
CN109954484A (en) * 2019-04-04 2019-07-02 哈尔滨工程大学 The uranium absorption material and preparation method of mesoporous silica gel particulate load amidoxim polymer
CN110280228A (en) * 2019-07-05 2019-09-27 湖南嘉沣工程设计有限责任公司 A method of preparing absorbent-type mesoporous microsphere

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130168322A1 (en) * 2010-09-14 2013-07-04 Kaneka Corporation Amidoxime-modified polyacrylonitrile porous body
CN105924657A (en) * 2016-06-03 2016-09-07 广东工业大学 Preparation method of electrostatic spray nano microsphere with porous structure
CN107913677A (en) * 2017-12-12 2018-04-17 成都育芽科技有限公司 A kind of nanometer heavy metal wastewater thereby ionic adsorption microballoon and preparation method thereof
CN109364891A (en) * 2018-11-14 2019-02-22 上海交通大学 A kind of modified polyacrylonitrile and preparation method thereof handling stibium-containing wastewater
CN109954484A (en) * 2019-04-04 2019-07-02 哈尔滨工程大学 The uranium absorption material and preparation method of mesoporous silica gel particulate load amidoxim polymer
CN110280228A (en) * 2019-07-05 2019-09-27 湖南嘉沣工程设计有限责任公司 A method of preparing absorbent-type mesoporous microsphere

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116747715A (en) * 2023-04-14 2023-09-15 浙江大学 High-water flux nanofiltration membrane with gradient structure separation layer and preparation method thereof
CN116747715B (en) * 2023-04-14 2024-01-23 浙江大学 High-water flux nanofiltration membrane with gradient structure separation layer and preparation method thereof

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