Magnetic polymer adsorption material, preparation method therefor and application thereof

Abstract

A magnetic polymer adsorption material, preparation method and use thereof, which relate to the field of magnetic polymer materials. The preparation method comprises: (1) preparing magnetic nanoparticles; (2) dissolving the magnetic nanoparticles in a pore-forming agent, adding N-vinylpyrrolidone, divinylbenzene and an initiator respectively, and mixing uniformly; (3) adding an emulsifier and a dispersant into an aqueous solution; adding a part of the oil phase solution prepared in step (2) at the temperature below 60° C., and adding the rest of the oil phase solution when the temperature rises to 60° C. or above, reacting with stirring, precipitating and filtering the reacted solution, washing and drying the precipitate, and finally obtaining the magnetic polymer adsorption material. The material has the particle size of 2-100 μm, the magnetization of 5-19.5 emu/g and the specific surface area of 210-950 m.sup.2/g, and can be applied to the adsorption of inorganic and organic matters in solutions, the controlled release of inorganic and organic matters, and the separation of different substances.

Claims

1. A method for preparing a magnetic polymer adsorption material, comprising the following steps: (1) preparing magnetic nanoparticles; (2) formulating a first solution comprising the steps of: dissolving the magnetic nanoparticles prepared in step (1) in an agent, adding N-vinylpyrrolidone, divinylbenzene and an initiator respectively, and mixing uniformly under the condition of ice bath; and (3) synthesizing the magnetic polymer adsorption material comprising the steps of: adding an emulsifier and/or a dispersant into an aqueous solution; adding a part of the first solution prepared in step (2) at the temperature below 60° C. into said aqueous solution, and adding the rest of the first solution when the temperature rises to 60° C. or above, wherein the volume of the first solution added each time accounts for 10-90% of the total volume of the total first solution, reacting with stirring, then precipitating and filtering the reacted solution, washing and drying the precipitate, and finally obtaining the magnetic polymer adsorption material.

2. The method for preparing a magnetic polymer adsorption material according to claim 1, wherein the magnetic nanoparticles are Fe.sub.3O.sub.4 organic acid nanoparticles, and the preparation process comprises: formulating soluble salts of Fe.sup.2+ and Fe.sup.3+ into a solution, mixing, introducing nitrogen for protection, adding a precipitating agent and an organic acid at 60-100° C., reacting for 0.5-12 h, adjusting the pH of the solution to be acidic, and washing and drying the product to obtain the magnetic Fe.sub.3O.sub.4 organic acid nanoparticles.

3. The method for preparing a magnetic polymer adsorption material according to claim 1, wherein in step (3), the stirring is performed at 100-1500 rpm for 12-80 h, and the reaction with stirring is performed at 60-95° C.

4. The method for preparing a magnetic polymer adsorption material according to claim 1, wherein the mass of the N-vinylpyrrolidone accounts for 10-90% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

5. The method for preparing a magnetic polymer adsorption material according to claim 1, wherein the volume of the agent is 0.05-2 times that of the aqueous solution; the mass of the emulsifier or dispersant accounts for 0.1-10% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; and the mass of the initiator accounts for 0.1-5% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

6. The method for preparing a magnetic polymer adsorption material according to claim 2, wherein the initiator is an azo or benzoyl compound; the agent is one or more of methanol, toluene, cyclohexanol, Dimethylformamide and Dimethyl sulfoxide; the emulsifier is an anionic surfactant; the dispersant is one or more of Polyvinylpyrrolidone, Hydroxyethylcellulose and Polyethylene glycol; the molar ratio of the soluble salt of Fe.sup.2+ to the soluble salt of Fe.sup.3+ is 1:(0.23-5.5); the mass of the organic acid is 0.5-5 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; and the precipitating agent is an alkaline solution.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic diagram of the basic structure of the magnetic polymer adsorption material according to the present invention;

(2) FIG. 2 is a Fourier transform infrared (FT-IR) spectrum of the magnetic polymer adsorption material according to the present invention; and

(3) FIG. 3 is a scanning electron microscope (SEM) image of the magnetic polymer adsorption material according to the present invention.

DETAILED DESCRIPTION

(4) The present invention is further described below with reference to specific examples. The following examples are merely used to explain the technical solutions and cannot be used to limit the protection scope of the present invention.

Example 1

(5) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(6) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 1 g of ferrous chloride, 2 g of ferric chloride and 100 mL water were added into a 250 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 4 mol/L sodium hydroxide solution and 0.75 g of oleic acid were added at 60° C., at this point, the mass of the oleic acid was 0.5 time that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 10 h, the pH of the solution was adjusted to 3; the product was washed with water and ethanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(7) (2) Formulation of the oil phase solution: 2 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 30 mL of toluene solution, and 3 g of N-vinylpyrrolidone, 3 g of divinylbenzene and 0.05 g of AIBN were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 50% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator AIBN accounted for 0.8% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(8) (3) Synthesis of the magnetic polymer adsorption material: 0.5 g of emulsifier SDS and 0.25 g of dispersant HEC were added into 50 mL of aqueous solution; half of the oil phase solution was added at 45° C. and the other half of the oil phase solution at 65° C., wherein the mass of the emulsifier accounted for 8.3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersant accounted for 4.2% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 24 h at 300 rpm, 65° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 65° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(9) The basic structure of the material is shown in FIG. 1. According to the reaction mechanism, the two double bonds of the monomer divinylbenzene added may be opened for chain propagation; and monomer radicals activated in the reaction can form new radicals with the N-vinylpyrrolidone, the divinylbenzene or the magnetic nanoparticles containing oleic acid to perform chain propagation until chain termination.

(10) The structural characterization diagram of FTIR of the material is shown in FIG. 2. The characteristic peak at 1690 cm.sup.−1 is the C═O bond of the N-vinylpyrrolidone, 707 cm.sup.−1 and 796 cm.sup.−1 are the characteristic peaks of benzene ring, and 3430 cm.sup.−1 and 585 cm.sup.−1 are the characteristic peaks of Fe.sub.3O.sub.4 nanoparticles.

(11) The SEM image of the material is shown in FIG. 3. The particle size of the magnetic polymer adsorption material is concentrated at 100 μm. It can be seen from FIG. 1, the particle size distribution of the material is relatively uniform, and its specific surface area is 681.5 m.sup.2/g as measured by the automatic specific surface area and porosity analyzer, its magnetization is 15 emu/g as measured by the vibrating sample magnetometer. The experiments have shown that the adsorption capacity of the magnetic polymer adsorption material to the nitrobenzene compounds in water is 389 mg/g at 25° C.

(12) The adsorption capacity of Oasis HLB material with the same specific surface area produced commercially by Waters Corporation is only 157 mg/g, and that of commercial XAD-4 resin is only 25.7 mg/g. The material prepared in this example has a significant increase in the adsorption of pollutants. After the adsorption experiment, only an external magnet is needed to separate the adsorption material from the solution; compared with the commercial Oasis HLB and XAD-4 resin, the post-treatment of the material prepared in this example is simple, feasible and convenient.

Comparative Example A

(13) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 1 g of ferrous chloride, 2 g of ferric chloride and 100 mL water were added into a 250 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 4 mol/L sodium hydroxide solution and 4 g of oleic acid were added at 60° C., at this point, the mass of the oleic acid was 0.9 time that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 10 h, the pH of the solution was adjusted to 3, the product was washed with water and ethanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(14) (2) N-vinylpyrrolidone, divinylbenzene, a pore-forming agent toluene and an initiator AIBN were mixed, and then the mixture was added into a three-necked flask containing anhydrous ethanol as organic phase, followed by the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles in step (1); after reaction with heating for a certain time, the product was filtered, washed and dried.

(15) After testing, the magnetization of the material prepared in the foregoing steps is very small (<0.1 emu/g), which cannot be magnetically separated in the solution. It is not possible to synthesize the magnetic polymer adsorption materials by changing the way of adding magnetic nanoparticles and the proportion of addition many times.

Comparative Example B

(16) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 1 g of ferrous chloride, 2 g of ferric chloride and 100 mL water were added into a 250 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 4 mol/L sodium hydroxide solution and 4 g of oleic acid were added at 60° C., at this point, the mass of the oleic acid was 0.9 time that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 10 h, the pH of the solution was adjusted to 3, the product was washed with water and ethanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(17) (2) N-vinylpyrrolidone, divinylbenzene, a pore-forming agent toluene and an initiator AIBN were mixed, and then the mixture was added into an aqueous solution containing one or more of sodium chloride, gelatin, polyvinyl alcohol and a surfactant, then the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles in step (1); after reaction with heating for a certain time, the product was filtered, washed and dried.

(18) After testing, the magnetization of the material prepared in the foregoing steps is very small (<0.3 emu/g), which cannot be magnetically separated in the solution. It is not possible to synthesize the magnetic polymer adsorption material by changing the way of adding magnetic nanoparticles for many times.

(19) As seen from the Comparative Example A and Comparative Example B, according to the preparation method using N-vinylpyrrolidone and divinylbenzene as monomers in the prior art, it is difficult to introduce magnetic nanoparticles and prepare the magnetic polymer adsorption material.

Example 2

(20) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(21) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 2.6 g of ferrous chloride, 6.4 g of ferric chloride and 200 mL water were added into a 500 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 40 mL of 2 mol/L potassium hydroxide solution and 4 g of oleic acid were added at 100° C., wherein the mass of the oleic acid was twice that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 6 h, the pH of the solution was adjusted to 3; the product was washed with water and methanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(22) (2) Formulation of the oil phase solution: 1 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 10 mL of cyclohexanol solution, and 2 g of N-vinylpyrrolidone, 1.5 g of divinylbenzene and 0.07 g of AIBN were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 57% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator AIBN accounted for 2% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(23) (3) Synthesis of the magnetic polymer adsorption material: 0.1 g of emulsifier SDS and 0.05 g of dispersant HEC were added into 200 mL of aqueous solution; 10% of the oil phase solution was added at 45° C. and the rest of the oil phase solution at 65° C., wherein the mass of the emulsifier accounted for 2.9% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersant accounted for 1.45% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 48 h at 500 rpm, 65° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 75° C. for 24 h to finally obtain the magnetic polymer adsorption material.

(24) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 10 μm, the specific surface area of 714 m.sup.2/g and the magnetization of 12 emu/g. The adsorption capacity of the material to tetracycline in water was 275 mg/g at 25° C. The magnetic polymer material saturated by tetracycline adsorption was separated by an external magnetic field and then added into pure water for ultrasonic treatment, and the ultrasonic power and time could be adjusted to control the content of tetracycline released in the water. Therefore, the material can also be used for the controlled release of tetracycline.

Example 3

(25) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(26) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 1 g of ferrous chloride, 7 g of ferric chloride and 100 mL water were added into a 250 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of saturated ammonia solution and 3 g of oleic acid were added at 70° C., wherein the mass of the oleic acid was 1.7 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 0.5 h, the pH of the solution was adjusted to 3; the product was washed with water and methanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(27) (2) Formulation of the oil phase solution: 2 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 30 mL of DMF solution, and 3 g of N-vinylpyrrolidone, 2 g of divinylbenzene and 0.1 g of BPO were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 60% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator BPO accounted for 2% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(28) (3) Synthesis of the magnetic polymer adsorption material: 0.005 g of emulsifier SDS and 0.5 g of dispersant PVP were added into 100 mL of aqueous solution; half of the oil phase solution was added at 55° C. and the other half of the oil phase solution at 75° C., wherein the mass of the emulsifier accounted for 0.1% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersant accounted for 10% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 24 h at 300 rpm, 75° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 65° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(29) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 120 μm, the specific surface area of 254 m.sup.2/g and the magnetization of 9 emu/g. The adsorption capacity of the material to copper ions in water was 75 mg/g at 25° C. The magnetic polymer material saturated by copper ion adsorption was separated by an external magnetic field and then added into 0.1 mol/L hydrochloric acid solution, so that the copper ions could be released completely. Therefore, the material can also be used for the controlled release of copper ions.

Example 4

(30) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(31) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 3 g of ferrous chloride, 8 g of ferric chloride and 100 mL water were added into a 500 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 4 mol/L sodium hydroxide solution and 7 g of oleic acid were added at 80° C., wherein the mass of the oleic acid was 1.2 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 6 h, the pH of the solution was adjusted to 3; the product was washed with water and ethanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(32) (2) Formulation of the oil phase solution: 2 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 60 mL of DMSO solution, and 2 g of N-vinylpyrrolidone, 4 g of divinylbenzene and 0.01 g of BPO were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 33% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator BPO accounted for 0.2% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(33) (3) Synthesis of the magnetic polymer adsorption material: 0.5 g of emulsifier SDS, 0.2 g of dispersant PEG and 0.075 g of dispersant HEC were added into 30 mL of aqueous solution; 90% of the oil phase solution was added at 40° C. and the rest of the oil phase solution at 64° C., wherein the mass of the emulsifier accounted for 8.3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersants accounted for 4.6% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 12 h at 800 rpm, 64° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 65° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(34) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 70 μm, the specific surface area of 414 m.sup.2/g and the magnetization of 9 emu/g. The adsorption capacity of the material to triclosan (10 ppm) in water was 115 mg/g at 25° C. 100 mg of magnetic polymer material saturated by triclosan adsorption was separated by an external magnetic field and then added into 1 mL of methanol solvent, so that the adsorbed triclosan could be completely released after shaking. Therefore, the material can also be used for the controlled release of triclosan.

Example 5

(35) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(36) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 3 g of ferrous chloride, 1 g of ferric chloride and 200 mL water were added into a 500 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 2 mol/L sodium hydroxide solution and 3 g of oleic acid were added at 80° C., wherein the mass of the oleic acid was 4.5 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 7 h, the pH of the solution was adjusted to 2; the product was washed with water and methanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(37) (2) Formulation of the oil phase solution: 2 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 10 mL of cyclohexanol solution, and 3.5 g of N-vinylpyrrolidone, 2.5 g of divinylbenzene and 0.006 g of AIBN were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 58% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator BPO accounted for 0.1% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(38) (3) Synthesis of the magnetic polymer adsorption material: 0.3 g of emulsifier SDS and 0.15 g of dispersant HEC were added into 50 mL of aqueous solution; 40% of the oil phase solution was added at 55° C. and the rest of the oil phase solution at 95° C., wherein the mass of the emulsifier accounted for 5% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersant accounted for 2.5% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 80 h at 100 rpm, 95° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 85° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(39) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 100 μm, the specific surface area of 225 m.sup.2/g and the magnetization of 9.5 emu/g. The adsorption capacity of the material to triclosan (10 ppm) in water was 98.5 mg/g at 25° C.

Example 6

(40) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(41) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 1 g of ferrous chloride, 2.5 g of ferric chloride and 150 mL water were added into a 250 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of saturated ammonia solution and 10 g of oleic acid were added at 80° C., wherein the mass of the oleic acid was 5 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 5 h, the pH of the solution was adjusted to 1; the product was washed with water and methanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(42) (2) Formulation of the oil phase solution: 2 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 30 mL of DMF solution, and 0.5 g of N-vinylpyrrolidone, 4.5 g of divinylbenzene and 0.1 g of BPO were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 10% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator BPO accounted for 2% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(43) (3) Synthesis of the magnetic polymer adsorption material: 0.3 g of emulsifier SDS was added into 200 mL of aqueous solution; 45% of the oil phase solution was added at 55° C. and the rest of the oil phase solution at 60° C., wherein the mass of the emulsifier accounted for 6% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 48 h at 700 rpm, 60° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 75° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(44) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 40 μm, the specific surface area of 624 m.sup.2/g and the magnetization of 11.2 emu/g. The adsorption capacity of the material to zinc ions in water was 75.2 mg/g at 25° C.

Example 7

(45) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(46) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 5 g of ferrous chloride, 7 g of ferric chloride and 300 mL water were added into a 500 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 50 mL of 2 mol/L sodium hydroxide solution and 2 g of oleic acid were added at 70° C., wherein the mass of the oleic acid was 0.5 time that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 6 h, the pH of the solution was adjusted to 2; the product was washed with water and methanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(47) (2) Formulation of the oil phase solution: 1 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 20 mL of toluene solution, and 4.5 g of N-vinylpyrrolidone, 0.5 g of divinylbenzene and 0.1 g of AIBN were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 90% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator AIBN accounted for 2% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(48) (3) Synthesis of the magnetic polymer adsorption material: 1 g of emulsifier HTAB was added into 200 mL of aqueous solution; one third of the oil phase solution was added at 35° C. and the rest of the oil phase solution at 75° C., wherein the mass of the emulsifier accounted for 20% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 36 h at 1500 rpm, 75° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 75° C. for 24 h to finally obtain the magnetic polymer adsorption material.

(49) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 50 μm, the specific surface area of 772 m.sup.2/g and the magnetization of 19.5 emu/g.

Example 8

(50) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(51) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles: 5 g of ferrous chloride, 8 g of ferric chloride and 200 mL water were added into a 500 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 4 mol/L sodium hydroxide solution and 9 g of oleic acid were added at 80° C., wherein the mass of the oleic acid was 1.45 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 12 h, the pH of the solution was adjusted to 1; the product was washed with water and ethanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were obtained after drying.

(52) (2) Formulation of the oil phase solution: 2 g of the magnetic Fe.sub.3O.sub.4@ oleic acid nanoparticles were dissolved in 30 mL of DMSO solution, and 2 g of N-vinylpyrrolidone, 8 g of divinylbenzene and 0.5 g of BPO were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 20% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator BPO accounted for 5% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(53) (3) Synthesis of the magnetic polymer adsorption material: 0.3 g of emulsifier SDS, 0.22 g of dispersant PEG and 0.075 g of dispersant HEC were added into 150 mL of aqueous solution; 45% of the oil phase solution was added at 45° C. and the rest of the oil phase solution at 65° C., wherein the mass of the emulsifier accounted for 3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersants accounted for 3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 36 h at 600 rpm, 65° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 65° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(54) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 2 μm, the specific surface area of 950 m.sup.2/g and the magnetization of 15 emu/g. The adsorption capacity of the material to phenol (100 ppm) in water was 380.5 mg/g at 25° C.

Example 9

(55) In this example, the preparation of the magnetic polymer adsorption material comprises the following steps:

(56) (1) Preparation of the magnetic Fe.sub.3O.sub.4@ citric acid nanoparticles: 2.5 g of ferrous chloride, 4 g of ferric chloride and 200 mL water were added into a 500 mL flask, electrically stirring and mixing, and nitrogen was introduced for protection, and then 20 mL of 4 mol/L sodium hydroxide solution and 5 g of sodium citrate were added at 80° C., wherein the mass of the citric acid was 1.5 times that of the magnetic Fe.sub.3O.sub.4 nanoparticles; after reaction for 10 h, the pH of the solution was adjusted to 2; the product was washed with water and ethanol for 5 times, and the magnetic Fe.sub.3O.sub.4@ citric acid nanoparticles were obtained after drying.

(57) (2) Formulation of the oil phase solution: 2.2 g of the magnetic Fe.sub.3O.sub.4@ citric acid nanoparticles were dissolved in 30 mL of DMSO solution, and 2 g of N-vinylpyrrolidone, 8 g of divinylbenzene and 0.3 g of BPO were added respectively, and mixed uniformly under the ice bath to obtain the oil phase solution, wherein the mass of the N-vinylpyrrolidone accounted for 20% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the initiator BPO accounted for 3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene.

(58) (3) Synthesis of the magnetic polymer adsorption material: 0.3 g of emulsifier SDS, 0.22 g of dispersant PEG and 0.075 g of dispersant HEC were added into 150 mL of aqueous solution; 45% of the oil phase solution was added at 45° C. and the rest of the oil phase solution at 65° C., wherein the mass of the emulsifier accounted for 3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene, and the mass of the dispersants accounted for 3% of the total mass of the N-vinylpyrrolidone and the divinylbenzene; after stirring for 36 h at 600 rpm, 65° C., the reacted solution was precipitated and filtered, the precipitate was washed with methanol for 5 times, and dried at 65° C. for 12 h to finally obtain the magnetic polymer adsorption material.

(59) The magnetic polymer adsorption material obtained in this example had the particle size concentrated in 20 μm, the specific surface area of 345 m.sup.2/g and the magnetization of 10 emu/g. The adsorption capacity of the material to phenol (100 ppm) in water was 220.5 mg/g at 25° C.

(60) Table 1 shows the parameters and properties of the materials prepared in Examples 1-9.

(61) TABLE-US-00001 TABLE 1 Parameters and properties of the materials prepared in Examples 1-9 Specific Adsorbed Adsorption Example Particle size surface area Magnetization pollutants capacity Material of 100 μm 681.5 m.sup.2/g   15 emu/g Nitrobenzene 389 mg/g Example 1 compounds Material of 10 μm 714 m.sup.2/g 12 emu/g Tetracycline 275 mg/g Example 2 Material of 120 μm 254 m.sup.2/g 9 emu/g Copper ions 75 mg/g Example 3 Material of 70 μm 414 m.sup.2/g 9 emu/g Triclosan 115 mg/g Example 4 Material of 100 μm 225 m.sup.2/g 9.5 emu/g Triclosan 98.5 mg/g Example 5 Material of 40 μm 624 m.sup.2/g 11.2 emu/g Zinc ions 75.2 mg/g Example 6 Material of 50 μm 772 m.sup.2/g 19.5 emu/g — — Example 7 Material of 2 μm 950 m.sup.2/g 15 emu/g Phenol 380.5 mg/g Example 8 Material of 20 μm 345 m.sup.2/g 10 emu/g Phenol 220.5 mg/g Example 9 Comparative — — <0.1 emu/g — — Example A Comparative — — <0.3 emu/g — — Example B

(62) Since the material has adsorption and controlled release properties to multiple substances, it can be used for separation of different substances.

(63) The present invention and embodiments thereof have been schematically described above, and the description is not restrictive. The accompanying drawings show only one of the embodiments of the present invention, and the actual process is not limited thereto. Therefore, if a person of ordinary skill in the art designs similar structural modes and embodiments without creativity under the enlightenment without departing from the creation purpose of the present invention, the structural modes and the embodiments should fall within the protection scope of the present invention.