CN115028206A

CN115028206A - Janus two-dimensional magnetic nanoparticle and preparation method and application thereof

Info

Publication number: CN115028206A
Application number: CN202210704470.0A
Authority: CN
Inventors: 华朝; 张健; 唐晓旭; 王秀军; 孙哲; 陈翔宇; 李仕超; 侯胜珍; 王姗姗; 赵春花
Original assignee: Beijing Research Center of CNOOC China Ltd; CNOOC China Ltd
Current assignee: Beijing Research Center of CNOOC China Ltd; CNOOC China Ltd
Priority date: 2022-06-21
Filing date: 2022-06-21
Publication date: 2022-09-09
Anticipated expiration: 2042-06-21
Also published as: CN115028206B

Abstract

The invention relates to Janus two-dimensional magnetic nanoparticles and a preparation method and application thereof. The preparation method of the Janus two-dimensional magnetic nanoparticles comprises the following steps: adding melted paraffin into the aqueous dispersion of the two-dimensional magnetic nanoparticles, stirring, cooling to room temperature, and collecting and separating by a magnet to obtain paraffin spheres with the surfaces adsorbing the two-dimensional magnetic nanoparticles; dispersing paraffin spheres with two-dimensional magnetic nanoparticles adsorbed on the surfaces in an ethanol water solution, regulating the pH value to 8-9, adding n-octyl triethoxysilane for reaction, separating by using a magnet after the reaction is finished, and dissolving to remove the paraffin spheres to obtain Fe ₃ O ₄ @ OTES granules, dispersing in aqueous ethanol, adding N-aminoethyl-gamma-aminopropylThe trimethoxy silane is reacted, and the trimethoxy silane is obtained by magnet separation after the reaction is finished. The Janus two-dimensional magnetic nanoparticles prepared by the method through the interface protection method not only have the excellent properties of Janus sheet materials, but also have special magnetic responsiveness, so that the Janus two-dimensional magnetic nanoparticles are easier to recycle and reuse and reduce the cost after being used for preparing stable emulsion.

Description

Janus two-dimensional magnetic nanoparticle and preparation method and application thereof

Technical Field

The invention relates to a Janus two-dimensional magnetic nanoparticle and a preparation method and application thereof, and belongs to the technical field of preparation of nano materials.

Background

"Janus" was originally proposed by professor De Gennes in 1991 and mainly refers to two asymmetric materials of different chemical nature or different composition. The Janus nano material has unique properties, so that the application prospect is wide, and more researchers research the Janus nano material. Janus nanomaterials refer to particular materials having an asymmetric structure or property, including asymmetry in material morphology or asymmetry in compositional properties. From the aspect of morphology, the asymmetry of the morphology endows the Janus material with a special spatial effect; from a compositional standpoint, the two halves of the Janus material have two different properties, which may even be opposite, such as hydrophilic-lipophilic, polar-nonpolar, magnetic-nonmagnetic, and the like. Thus Janus materials have multiple functionalities and can meet more complex environmental requirements. The main preparation method comprises a boundary protection method, a microfluid method, a nucleation growth control method and the like. Since the first report of Granick, the use of paraffin interface protection method for preparing Janus particles has attracted great interest to scholars at home and abroad.

The two-dimensional magnetic nanoparticles have good yield and injection increasing effects, no toxicity, low price and special magnetic responsiveness, and are widely applied to various aspects of oil displacement, emulsion breaking, emulsion stabilization and the like. For Janus magnetic nano sheets, the Janus magnetic nano sheets not only have the excellent properties of Janus sheet materials, but also have multiple functions of intelligently finding oil, absorbing, stripping oil films, emulsifying and reducing viscosity, gathering oil walls and the like; but also has special magnetic response, and the formed emulsion is easier to recycle and reuse. Therefore, the high-stability Pickering emulsion formed by the Janus magnetic nanosheets is expected to play a greater role in the fields of chemical oil displacement, recovery efficiency improvement and the like. However, the research on preparing the high-stability Pickering emulsion by using the Janus magnetic nano sheets is few so far, and based on the research, a novel strategy for constructing the high-stability Pickering emulsion by using the Janus magnetic nano sheets is provided.

Disclosure of Invention

The invention aims to provide Janus two-dimensional magnetic nanoparticles and a preparation method thereof.

The Janus two-dimensional magnetic nanoparticles are prepared on the basis of two-dimensional magnetic nanoparticles, and the two-dimensional magnetic nanoparticles are prepared according to the following method:

dropwise adding the aqueous solution of ferrous sulfate heptahydrate into the aqueous solution of sodium hydroxide and sodium acetate, and reacting under the condition of stirring; and after the reaction is finished, collecting and separating by using a magnet to obtain the two-dimensional magnetic nanoparticles.

Specifically, the reaction temperature is 50-80 ℃, preferably 60 ℃, and the two-dimensional magnetic nanoparticles prepared at the temperature are regular in shape, uniform in size and uniform in particle size;

under the condition of water bath.

Specifically, the stirring speed is 200-600 rpm, preferably 500rpm, the two-dimensional magnetic nanoparticles prepared at the stirring speed are regular in shape, most of the particles are hexagonal, and the size of the particles is relatively uniform.

Specifically, the reaction time is 2-3 h, preferably 2h, and most products of the two-dimensional magnetic nanoparticles prepared under the reaction time are hexagonal and regular in shape.

Specifically, the dropping speed of the aqueous solution of ferrous sulfate heptahydrate is 2-2.4 mL/min, preferably 2.4mL/min, and when the aqueous solution of ferrous sulfate heptahydrate is dropped at the speed, most of generated products are two-dimensional sheet structures, the shapes are regular, and the distribution is uniform.

Specifically, in the aqueous solution of the ferrous sulfate heptahydrate, the molar concentration of the ferrous sulfate heptahydrate is 0.096-0.144 mol/L, preferably 0.096mol/L, and the product prepared under the concentration has a two-dimensional sheet structure and a regular shape.

Specifically, in the aqueous solution of sodium hydroxide and anhydrous sodium acetate, the molar concentration of the sodium hydroxide is 0.18-0.27 mol/L, preferably 0.18mol/L, the particle size of the magnetic nanoparticles prepared under the concentration is small, and the product is mostly in a two-dimensional sheet structure and regular in shape;

the molar concentration of the anhydrous sodium acetate is 0.9-1.35 mol/L, preferably 0.9mol/L, and the magnetic nanoparticles prepared under the concentration are regular in shape and similar in structure.

The thickness of the two-dimensional magnetic nanoparticles prepared by the method is about 4.2-4.6 nm.

The two-dimensional magnetic nanoparticles prepared by the method have smooth surfaces and uniform thickness.

The magnetism of the prepared two-dimensional magnetic nanoparticles is measured by adopting VSM, at room temperature, the saturation magnetization (Ms) of the magnetic nanosheet is 77.5emu/g, the residual magnetization (Mr) is 11.2emu/g, the coercive force (Hc) is 106.7Oe, and the magnetic nanosheet has good magnetism and can be used as a good magnetic material. Meanwhile, under the action of an external magnetic field, the magnetic field can be quickly separated from liquid, so that recovery and reutilization can be realized, and the cost is reduced.

XRD, HRTEM, XPS and FT-IR are adopted to carry out two-dimensional magnetic nano-particlesThe phase and crystal structure analysis of the particles is carried out, and the two-dimensional magnetic nano particles prepared by the invention are definitely Fe ₃ O ₄ The naked surface is (111) surface, and the synthesized two-dimensional magnetic nano-sheet is a hexagon with a regular shape and belongs to anisotropic nano-particles.

The preparation method of the Janus two-dimensional magnetic nanoparticles provided by the invention comprises the following steps:

s1, adding melted paraffin into the aqueous dispersion of the two-dimensional magnetic nanoparticles, stirring, cooling to room temperature, and collecting and separating by a magnet to obtain paraffin spheres with the surfaces adsorbing the two-dimensional magnetic nanoparticles;

s2, dispersing the paraffin spheres with the surfaces adsorbing the two-dimensional magnetic nanoparticles in an ethanol water solution, regulating the pH value to 8-9, adding n-octyl triethoxysilane (or other silane coupling agents) for reaction, separating by using a magnet after the reaction is finished, and dissolving to remove the paraffin spheres to obtain Fe ₃ O ₄ @ OTES particles;

s3, mixing the Fe ₃ O ₄ The @ OTES particles are dispersed in ethanol water solution, N-aminoethyl-gamma-aminopropyltrimethoxysilane (or other silane coupling agents) is added for reaction, and the Janus two-dimensional magnetic nanoparticles are obtained through magnet separation after the reaction is finished.

In the preparation method, in step S1, stirring is carried out at 20-40 ℃;

in the aqueous dispersion, the concentration of the two-dimensional magnetic nanoparticles is 1-4 mg/mL;

in the steps S2 and S3, the volume fraction of water in the ethanol water solution is 1-2%;

in step S2, adjusting the pH value with sodium hydroxide aqueous solution;

the dosage of the n-octyl triethoxysilane is as follows: 1g: 0.5-2 mL of the n-octyltriethoxysilane;

the reaction temperature is 20-40 ℃, and the reaction time is 10-20 h.

In the above preparation method, in step S3, the dosage of N-aminoethyl- γ -aminopropyltrimethoxysilane is: 0.25 to 1mL of the N-aminoethyl-gamma-aminopropyltrimethoxysilane;

the reaction temperature is 20-40 ℃, and the reaction time is 10-20 h.

According to the invention, the morphology of the prepared product is analyzed through TEM and HRTEM, and the coating thickness is determined to be about 3.85 nm.

According to the contact angle and interface property analysis of the Janus two-dimensional magnetic nanoparticles, the Janus two-dimensional magnetic nanoparticles can obviously reduce the toluene/water interface tension, and the influence of the Janus two-dimensional magnetic nanoparticles on an oil/water interface is analyzed.

The magnetic property of the Janus two-dimensional magnetic nanoparticles is measured by adopting VSM, the saturation magnetization (Ms) of the Janus two-dimensional magnetic nanoparticles is 48.9emu/g at room temperature, and the Janus two-dimensional magnetic nanoparticles can be separated from liquid within 60s under the action of an external magnetic field.

The Janus two-dimensional magnetic nanoparticles prepared by the method can be further used for preparing Pickering emulsion, and can be prepared according to the following method:

dispersing the Janus two-dimensional magnetic nanoparticles into a mixed system of an oil phase and a water phase, and obtaining the magnetic nanoparticles through dispersion;

the volume ratio of the oil phase to the water phase is 1: 1-2;

in the mixed system, the mass fraction of the Janus two-dimensional magnetic nanoparticles is 0.5 wt% -2 wt%.

The oil phase is dodecane, n-hexane, dichloromethane or butyl butyrate, namely the Janus two-dimensional magnetic nanoparticles can form stable emulsion with the dodecane and the n-hexane with weak polarity, and can form emulsion with dichloromethane or even butyl butyrate with slightly strong polarity.

Compared with the prior art, the Janus two-dimensional magnetic nanoparticles prepared by the method through the interface protection method have the excellent properties of Janus sheet materials and special magnetic responsiveness, so that the formed emulsion is easier to recycle and reuse. The high-stability Pickering emulsion formed by the Janus two-dimensional magnetic nanoparticles is expected to play a greater role in the fields of chemical oil displacement, recovery efficiency improvement and the like.

Drawings

FIG. 1 is a TEM image of two-dimensional magnetic nanoparticles at different reaction temperatures (FIG. 1(a)40 deg.C, FIG. 1(b)50 deg.C, FIG. 1(c)60 deg.C, FIG. 1(d)70 deg.C, FIG. 1(e)80 deg.C).

Fig. 2 is a graph showing the change of the average particle diameter of the two-dimensional magnetic nanoparticles according to the reaction temperature.

FIG. 3 is a graph showing the distribution of the two-dimensional magnetic nanoparticles in particle size at different reaction temperatures.

FIG. 4 is a TEM image of two-dimensional magnetic nanoparticles at different stirring speeds (FIG. 4(a)200rpm, FIG. 4(b)300rpm, FIG. 4(c)400rpm, FIG. 4(d)500rpm, FIG. 4(e)600 rpm).

Fig. 5 is a graph showing the change in the average particle diameter of two-dimensional magnetic nanoparticles with stirring speed.

FIG. 6 is a distribution diagram of two-dimensional magnetic nanoparticle sizes at different stirring speeds.

Fig. 7 is TEM images of two-dimensional magnetic nanoparticles at different reaction times (fig. 7(a)1h, fig. 7(b)2h, fig. 7(c)3h, fig. 7(d)4h, fig. 7(e)5 h).

Fig. 8 is a graph showing the change in the average particle diameter of two-dimensional magnetic nanoparticles with reaction time.

FIG. 9 is a graph showing the distribution of the two-dimensional magnetic nanoparticles in terms of particle size for different reaction times.

FIG. 10 shows different Fe ²⁺ TEM images of two-dimensional magnetic nanoparticles at dropping speed (FIG. 10(a)6mL/min, FIG. 10(b)4mL/min, FIG. 10(c)3mL/min, FIG. 10(d)2.4mL/min, FIG. 10(e)2 mL/min).

FIG. 11 shows the average particle size of two-dimensional magnetic nanoparticles as a function of Fe ²⁺ Graph showing the change in dropping rate.

FIG. 12 shows different Fe ²⁺ The distribution diagram of the particle size of the two-dimensional magnetic nanoparticles under the dropping speed.

FIG. 13 shows different Fe ²⁺ TEM images of two-dimensional magnetic nanoparticles at concentration (FIG. 13(a)0.048mol/L, FIG. 13(b)0.096mol/L, FIG. 13(c)0.144mol/L, FIG. 13(d)0.192 mol/L).

FIG. 14 shows the average particle size of two-dimensional magnetic nanoparticles as a function of Fe ²⁺ Graph of the change in concentration.

FIG. 15 shows different Fe ²⁺ Distribution diagram of particle size of two-dimensional magnetic nanoparticles under concentration。

FIG. 16 is TEM image of two-dimensional magnetic nanoparticles at different precipitant concentrations (0.09mol/L in FIG. 16(a), 0.18mol/L in FIG. 16(b), 0.27mol/L in FIG. 16(c), and 0.36mol/L in FIG. 16 (d)).

Fig. 17 is a graph of the change in the average particle size of two-dimensional magnetic nanoparticles with the concentration of the precipitant.

Fig. 18 is a graph of the distribution of the particle size of two-dimensional magnetic nanoparticles at different precipitant concentrations.

FIG. 19 is a TEM image of two-dimensional magnetic nanoparticles at different electrostatic stabilizer concentrations (FIG. 19(a)0.45mol/L, FIG. 19(b)0.9mol/L, FIG. 19(c)1.35mol/L, FIG. 19(d)1.8 mol/L).

Fig. 20 is a graph showing the change in the average particle diameter of two-dimensional magnetic nanoparticles with the concentration of the electrostatic stabilizer.

Fig. 21 is a graph of the distribution of the particle size of two-dimensional magnetic nanoparticles at different electrostatic stabilizer concentrations.

Fig. 22 is an XRD spectrum of two-dimensional magnetic nanoparticles at different stirring speeds.

Fig. 23 is an XRD spectrum of two-dimensional magnetic nanoparticles at different reaction temperatures.

Fig. 24 is an HRTEM picture, FFT (upper left corner) and partial magnified view of a two-dimensional magnetic nanoparticle.

Fig. 25 is a Fe2p, O1s XPS spectrum of a two-dimensional magnetic nanoparticle.

Fig. 26 is an infrared spectrum of a two-dimensional magnetic nanoparticle.

Fig. 27 is an AFM image of a two-dimensional magnetic nanoparticle.

Fig. 28 shows the line segment thickness between the line segments in the AFM image (between fig. 28(a) a and B, between fig. 28(B) C and D, and between fig. 28(C) E and F).

Fig. 29 is a TEM image of two-dimensional magnetic nanoparticles.

Fig. 30 is an AFM 3D map of a two-dimensional magnetic nanoparticle.

Fig. 31 is a hysteresis loop of a two-dimensional magnetic nanoparticle.

Fig. 32 is a photograph showing the magnetic separation process of two-dimensional magnetic nanoparticles (fig. 32(a) after 1min of ultrasound, fig. 32(b) after 15s of magnet separation, and fig. 32(c) after 30s of magnet separation).

FIG. 33 is a schematic diagram of Janus two-dimensional magnetic nanoparticle synthesis.

Fig. 34 is an SEM image of paraffin spheres formed by two-dimensional magnetic nanoparticles (fig. 34(b)6000x, fig. 34(c)12000 x).

Fig. 35 is a TEM image of Janus two-dimensional magnetic nanoparticles.

Fig. 36 is an HRTEM of Janus two-dimensional magnetic nanoparticles.

Fig. 37 is an infrared spectrum of Janus two-dimensional magnetic nanoparticles.

Fig. 38 shows the element distribution and composition on the surface of Janus two-dimensional magnetic nanoparticles.

Fig. 39 is a photograph showing the water contact angle of Janus two-dimensional magnetic nanoparticles (fig. 39(a) hydrophilic surface, and fig. 39(b) hydrophobic surface).

Fig. 40 is the interfacial tension of Janus two-dimensional magnetic nanoparticles.

FIG. 41 shows the effect of Janus two-dimensional magnetic nanoparticles on the oil-water interface (FIG. 41(a) toluene/water mixture in glass vessel, FIG. 41(b) Janus Fe at toluene/water interface after injection ₃ O ₄ FIG. 41(c) interfacial and climbing membrane formation after shaking; FIG. 41(d) dichloromethane/water mixture in glass vessel, FIG. 41(e) Janus Fe at dichloromethane/water interface after injection ₃ O ₄ FIG. 41(f) interfacial film and climbing film formation after shaking).

Fig. 42 shows the interfacial film deformation caused by Janus two-dimensional magnetic nanoparticles (fig. 42(a) is inserted into a capillary, fig. 42(b) is attracted by a magnet, and fig. 42(c) is removed from the magnet).

Fig. 43 is a hysteresis loop of Janus two-dimensional magnetic nanoparticles.

Fig. 44 is a photograph showing the magnetic separation process of Janus two-dimensional magnetic nanoparticles (fig. 44(a) after 1min of sonication, fig. 44(b) after 30s of magnetic separation, and fig. 44(c) after 60s of magnetic separation).

Fig. 45 is an optical microscope image of Pickering emulsion prepared from different mass fractions of Janus two-dimensional magnetic nanoparticles and dodecane (fig. 45(a)0.5 wt%, fig. 45(b)1.0 wt%, fig. 45(c)1.5 wt%, fig. 45(d)2.0 wt%).

Fig. 46 is an optical microscope image of Pickering emulsion prepared from Janus two-dimensional magnetic nanoparticles and different oil phases (fig. 46(a) dodecane, fig. 46(b) n-hexane, fig. 46(c) dichloromethane, and fig. 46(d) butyl butyrate).

Detailed Description

The experimental procedures used in the following examples are all conventional procedures unless otherwise specified.

Materials, reagents and the like used in the following examples are commercially available unless otherwise specified.

Example 1 preparation of two-dimensional magnetic nanoparticles

0.4g of sodium hydroxide and 4.1g of anhydrous sodium acetate are weighed into a beaker, 55g of deionized water is added into the beaker to prepare a solution, and the solution is transferred into a four-neck flask after ultrasonic dissolution. The four-neck flask is placed in a 60 ℃ water bath kettle, the mechanical stirring speed is set to be 500rpm, the reaction temperature is 60 ℃, and the reaction time is 2 hours. 1.6g of FeSO are weighed ₄ ·7H ₂ And O, adding 60g of deionized water into a beaker to prepare a solution, transferring the solution into a 60mL syringe after ultrasonic dissolution, putting the syringe into a constant flow pump, setting the dropping time of the constant flow pump to be 25min, and gradually dropping the solution into a four-neck flask. After the reaction is finished, collecting and separating the black two-dimensional magnetic nanoparticles by using a magnet, and washing the black two-dimensional magnetic nanoparticles by using deionized water and absolute ethyl alcohol for a plurality of times. And (4) placing the product in a freeze dryer, freeze-drying for 24 hours, and collecting the product to be tested.

Next, the reaction temperature, the stirring speed, the reaction time, and Fe were examined ²⁺ Dropping Rate, Fe ²⁺ The influence of concentration, precipitant concentration, electrostatic stabilizer concentration on the morphology and size of the two-dimensional magnetic nanoparticles.

Example 2 influence of reaction temperature on morphology and size of two-dimensional magnetic nanoparticles

The temperature is an important influence factor of crystal formation, and as the temperature is increased, the heat provided per unit time is increased, which is helpful for overcoming the reaction energy barrier and accelerating the crystal formation. Under otherwise identical conditions (stirring speed 500rpm, reaction time 2h, Fe) ²⁺ The dropping speed is 2.4mL/min, Fe ²⁺ Concentration of 0.096mol/L, precipitant concentration of 0.18mol/L, electrostatic stabilizer concentration of 0.9mol/L), only the reaction in the preparation process of the two-dimensional magnetic nanoparticles was changedThe two-dimensional magnetic nanoparticles were prepared at five different reaction temperatures (40 ℃, 50 ℃, 60 ℃, 70 ℃, 80 ℃).

Fig. 1 is a transmission electron microscope photograph of two-dimensional magnetic nanoparticles at different reaction temperatures, and fig. 2 is a graph of the change of the average particle size of the two-dimensional magnetic nanoparticles with the reaction temperature. As can be seen from fig. 1 and 2, the particle size of the two-dimensional magnetic nanoparticles gradually increases with the increase of the reaction temperature. When the reaction temperature is 40 ℃, the resulting product is mostly a large aggregate having no regular shape (fig. 1 (a)). As shown in fig. 1(b) and fig. 1(c), with the increasing temperature, nanosheets with shapes similar to hexagons appear, and when the temperature reaches 60 ℃, the two-dimensional magnetic nanoparticles are regular in shape and uniform in size. As the reaction temperature continues to increase, the shape of the two-dimensional magnetic nanoparticles is still mostly hexagonal, but the particle size is not uniform (fig. 1(d) and fig. 1 (e)). This was again demonstrated by the change in average particle size at 40 deg.C, 50 deg.C, 60 deg.C, 70 deg.C, and 80 deg.C, which correspond to 25.59nm, 37.90nm, 46.74nm, 48.74nm, and 50.65nm, respectively. In order to accurately know the particle size distribution condition of the nano particles in the system, the particle size is statistically analyzed. The particle size distribution of the two-dimensional magnetic nanoparticles at different reaction temperatures is shown in fig. 3. As seen from FIG. 3, the particle size distribution of the nanoparticles gradually increased with the increase of the reaction temperature, which is consistent with the observation results of the transmission electron microscope.

By analyzing TEM images of the two-dimensional magnetic nanoparticles and particle size distribution at different reaction temperatures, the two-dimensional magnetic nanoparticles have regular shapes and relatively uniform particle sizes at the reaction temperature of 60 ℃, and the reaction temperature of 60 ℃ is finally determined.

Example 3 Effect of stirring speed on morphology and size of two-dimensional magnetic nanoparticles

During crystal nucleation, there is a higher energy barrier. Different stirring speeds can provide different energies in the reaction process, and the input of external energy can accelerate the rapid formation of crystal nuclei, so that the stirring speed is also an important factor in the formation process of crystals. Under otherwise identical conditions (reaction temperature 6)At 0 ℃ for 2h, Fe ²⁺ The dropping speed is 2.4mL/min, Fe ²⁺ Concentration of 0.096mol/L, precipitant concentration of 0.18mol/L, and electrostatic stabilizer concentration of 0.9mol/L), two-dimensional magnetic nanoparticles were prepared at five different stirring speeds (200rpm, 300rpm, 400rpm, 500rpm, 600rpm) by changing only the stirring speed in the two-dimensional magnetic nanoparticle preparation process.

Fig. 4 is a transmission electron micrograph of the two-dimensional magnetic nanoparticles at different stirring speeds, and fig. 5 is a graph of the change of the average particle size of the two-dimensional magnetic nanoparticles with the stirring speed. As can be seen from fig. 4 and 5, the particle size of the two-dimensional magnetic nanoparticles as a whole tended to decrease with increasing stirring speed. As shown in fig. 4(a), when the stirring speed was 200rpm, the nanoparticles produced were regular in shape, hexagonal in morphology, but varied in size, and different nanoparticles were grown together. Under the condition of 300rpm, the particle size distribution of the two-dimensional magnetic nanoparticles is still relatively large, and the situation that different nanoparticles are combined together in the growth process still exists (fig. 4 (b)). From fig. 4(c) and 4(d), it can be seen that, with further increase of the stirring speed, under the conditions of 400rpm and 500rpm, the two-dimensional magnetic nanoparticles are regular in shape and relatively uniform in size, and the particle size distribution of the nanoparticles tends to decrease. As can be seen from fig. 4(e), when the stirring speed was increased to 600rpm, it was found that the difference in the size of the two-dimensional magnetic nanoparticles was further reduced and spherical particles appeared. Further examining the change of the average particle size of the two-dimensional magnetic nanoparticles with the stirring speed, the results are shown in FIG. 5. The average particle diameters at 200rpm, 300rpm, 400rpm, 500rpm and 600rpm of the stirring were 62.88nm, 60.50nm, 59.09nm, 46.74nm and 39.12nm, respectively. As can be seen from the change in the average particle size, the average particle size of the magnetic nanoparticles prepared under the change of the stirring speed continuously decreased as the stirring speed increased. FIG. 6 is a graph showing a distribution of the particle size of two-dimensional magnetic nanoparticles at different stirring speeds. As can be seen from fig. 6, the particle size distribution of the two-dimensional magnetic nanoparticles also gradually becomes smaller as the stirring speed increases, which is consistent with the results of the transmission electron microscope images.

On the whole, with the increase of the stirring rotating speed, the external input energy is continuously increased, the crystallization rate is accelerated, and the nano particles are rapidly nucleated. The crystal nucleation is relatively less at low rotation speed, so the particle size is larger, the particle size distribution is wider, and different nano particles grow and polymerize. Therefore, under the condition that the stirring rotating speed is increased continuously, the particle size of the magnetic nanosheets is gradually reduced, and the particle size distribution is gradually reduced. When the rotating speed reaches a certain degree, the growth crystal faces of the nano particles are changed, which is beneficial to the joint growth of all crystal faces, thereby leading to the appearance of spherical nano particles. From the results of analyzing the influence of the stirring speed on the two-dimensional magnetic nanoparticles, the two-dimensional magnetic nanoparticles are regular in shape, hexagonal in shape and relatively uniform in size under the condition that the stirring speed is 500rpm, and finally the stirring speed is preferably 500 rpm.

Example 4 Effect of reaction time on morphology and size of two-dimensional magnetic nanoparticles

The reaction time is also an important factor influencing the crystal growth, and with the increasing of the reaction time, an Ostwald ripening effect may exist, so that the reaction of the nanoparticles between the solid and liquid interfaces is reversible, and the two-dimensional magnetic nanoparticle appearance is greatly changed. Under otherwise identical conditions (reaction temperature 60 ℃, stirring speed 500rpm, Fe) ²⁺ The dropping speed is 2.4mL/min, Fe ²⁺ The concentration is 0.096mol/L, the precipitant concentration is 0.18mol/L, the electrostatic stabilizer concentration is 0.9mol/L), only the reaction time in the preparation process of the two-dimensional magnetic nanoparticles is changed, and the two-dimensional magnetic nanoparticles are prepared under five different reaction times (1h, 2h, 3h, 4h and 5 h).

Fig. 7 is a transmission electron micrograph of the two-dimensional magnetic nanoparticles at different reaction times, and fig. 8 is a graph of the change of the average particle size of the two-dimensional magnetic nanoparticles with time. As can be seen from fig. 7 and 8, the particle size of the two-dimensional magnetic nanoparticles gradually increases as the reaction time increases. As can be seen from fig. 7(a), the nanoparticles produced at a reaction time of 1h were relatively regular in shape, mostly hexagonal in structure, uniform in size, and small in overall particle size, but many rod-like structures were also produced. When the reaction time was 2 hours, it was found that most of the obtained products were hexagonal in shape, the particle size and distribution were increased as compared with 1 hour of nanoparticles, and the products having rod-like or spherical structures were relatively small (fig. 7 (b)). As shown in fig. 7(c), (d), and (e), as the reaction time continues to increase, the particle size of the magnetic nanoparticles gradually increases, and the particles are relatively uniform. The product produced contains a large amount of rod-shaped and spherical nanoparticles, although the two-dimensional plate-shaped nanoparticles are present in the product, the proportion of the two-dimensional plate-shaped nanoparticles tends to decrease. As shown in FIG. 8, the average particle diameters of the two-dimensional magnetic nanoparticles were further examined as a function of the reaction time, and the average particle diameters were 38.29nm, 46.74nm, 47.67nm, 48.74nm and 50.16nm at reaction times of 1h, 2h, 3h, 4h and 5h, respectively. As can be seen from the change of the average particle diameter with the reaction time, the average particle diameter of the magnetic nanoparticles continuously increases with the increase of the reaction time. When the reaction time is 2 hours, the particle size of the generated magnetic nanoparticles is obviously increased compared with that of the reaction time of 1 hour, and after the reaction time is 2 hours, the average particle size still tends to increase, but the difference is not large. FIG. 9 is a graph showing the distribution of the two-dimensional magnetic nanoparticles in terms of particle size for different reaction times. As shown in fig. 9, the particle size distribution of the two-dimensional magnetic nanoparticles shows a tendency to increase first and then decrease. When the reaction time reaches 3h, the particle size distribution is not greatly different.

According to analysis of a TEM image and a particle size distribution diagram of the two-dimensional magnetic nanoparticles, when the reaction time is 2h, most products are hexagonal and regular in shape, the reaction time is finally determined to be 2h, and on the basis, the influence of other conditions on the products is investigated.

Example 5 Fe ²⁺ Influence of dropping speed on morphology and size of two-dimensional magnetic nanoparticles

In the process of synthesizing the two-dimensional magnetic nanoparticles, the Fe is subjected to constant flow pump ²⁺ And (4) accurately controlling the dropping speed. Thus, in addition to taking into account the conventional influencing factors on nanoparticle formation, Fe was also investigated ²⁺ Dropwise addition ofThe effect of velocity on the growth of two-dimensional magnetic nanoparticles. Under the same conditions (reaction temperature of 60 ℃, stirring speed of 500rpm, reaction time of 2h, Fe) ²⁺ Concentration of 0.096mol/L, precipitant concentration of 0.18mol/L, electrostatic stabilizer concentration of 0.9mol/L), only changing Fe in the preparation process of the two-dimensional magnetic nanoparticles ²⁺ Dropping speed in five different Fe ²⁺ Two-dimensional magnetic nanoparticles were prepared at drop-wise rates (6mL/min, 4mL/min, 3mL/min, 2.4mL/min, 2 mL/min).

FIG. 10 shows two-dimensional magnetic nanoparticles at different Fe ²⁺ Transmission electron micrograph at dropping speed, FIG. 2.12 shows that the average particle size of the two-dimensional magnetic nanoparticles is dependent on Fe ²⁺ Graph showing the change in dropping rate. As shown in fig. 10 and 11, with Fe ²⁺ The dropping speed is reduced, and the particle size of the two-dimensional magnetic nanoparticles is gradually increased. As can be seen from FIG. 10(a), in Fe ²⁺ When the dropping speed is 6mL/min, the generated magnetic nanoparticles have different shapes, have hexagonal structures, triangular structures and linear structures, and are relatively small. When Fe ²⁺ When the dropping rate was 4mL/min or 3mL/min, it was found that the amount of Fe was changed ²⁺ The drop rate decreased to increase the particle size of the magnetic nanoparticles obtained, but many spherical particles remained. In Fe ²⁺ When the dropping rate was 3mL/min, many rod-like structures were present (FIG. 10(b) and FIG. 10 (c)). With Fe ²⁺ As shown in fig. 10(d) and 10(e), the dropping speed is further reduced, and it can be seen that the particle size of the magnetic nanoparticles gradually increases, and the majority of the generated products are nanoparticles with two-dimensional sheet structures, regular shapes, and relatively good dispersibility. As shown in FIG. 11, the average particle diameter of two-dimensional magnetic nanoparticles was examined as a function of Fe ²⁺ The relationship between the dropping speed and the drop velocity. In Fe ²⁺ The average particle diameters of the solution at the dropping speeds of 6mL/min, 4mL/min, 3mL/min, 2.4mL/min and 2mL/min were 39.41nm, 41.87nm, 44.21nm, 46.74nm and 48.00nm, respectively. As can be seen from the results of the variation of the average particle diameter, the average particle diameter of the magnetic nanoparticles is varied with Fe ²⁺ The dropping speed is reduced and increased. FIG. 12 shows different Fe ²⁺ At the dropping speedThe distribution of the two-dimensional magnetic nanoparticle size can be seen from FIG. 12, along with Fe ²⁺ The dropping speed is reduced, and the particle size distribution of the two-dimensional magnetic nanoparticles shows an increasing trend.

From the above results, it is clear that Fe is accompanied by Fe ²⁺ Decrease of dropping speed, Fe per unit time ²⁺ The concentration decreases, resulting in a decrease in the rate of nanoparticle nucleation. The nucleation quantity in unit time is less, and more Fe ²⁺ Acting on the already nucleated nanoparticles results in a gradual increase in the particle size and also in a larger particle size distribution. With Fe ²⁺ The dropping speed is reduced, and the formed magnetic nanoparticles are regular in shape and mostly have two-dimensional sheet structures. When viewed as a whole, Fe ²⁺ When the dripping speed is 2.4mL/min, most of the generated products are in two-dimensional sheet structures, the shapes are regular, the distribution is uniform, and finally the Fe is determined ²⁺ The dropping rate was 2.4 mL/min.

Example 6, Fe ²⁺ Effect of concentration on morphology and size of two-dimensional magnetic nanoparticles

In example 5, it was found that Fe is accompanied by Fe ²⁺ The appearance and the size of the two-dimensional magnetic nanoparticles are obviously changed by changing the dropping speed. From this it is seen that Fe ²⁺ Greatly influences the appearance and the size of the two-dimensional magnetic nano-particles, thereby further investigating Fe ²⁺ Effect of concentration on growth of two-dimensional magnetic nanoparticles. Under the same conditions (reaction temperature of 60 ℃, stirring speed of 500rpm, reaction time of 2h, Fe) ²⁺ The dropping speed is 2.4mL/min, the concentration of the precipitator is 0.18mol/L, the concentration of the electrostatic stabilizer is 0.9mol/L), and only the Fe in the preparation process of the two-dimensional magnetic nanoparticles is changed ²⁺ Concentration in four different Fe ²⁺ Two-dimensional magnetic nanoparticles were prepared at concentrations (0.048mol/L, 0.096mol/L, 0.144mol/L, 0.192 mol/L).

FIG. 13 shows two-dimensional magnetic nanoparticles at different Fe ²⁺ Transmission electron micrograph at concentration, FIG. 14 shows the mean particle size of two-dimensional magnetic nanoparticles with Fe ²⁺ Graph of the change in concentration. As shown in FIGS. 13 and 14, the particle size of the two-dimensional magnetic nanoparticles varied with Fe ²⁺ The increase in concentration shows a tendency to increase gradually. Such asFIG. 13(a) shows that when Fe ²⁺ At a concentration of 0.048mol/L, the magnetic nanoparticles produced have relatively small particle sizes and various shapes, and although there is a certain two-dimensional sheet structure, there are many rod-like and linear structures. As shown in FIG. 13(b), when Fe ²⁺ At a concentration of 0.096mol/L, the obtained magnetic nanoparticles had a large particle size, a two-dimensional sheet structure and a regular shape. As shown in FIGS. 13(c) and 13(d), when Fe ²⁺ When the concentration was further increased to 0.144 and 0.192mol/L, the nanoparticle diameter was further increased, and the shape was varied, and many spherical particles were present. As shown in FIG. 14, in Fe ²⁺ The average particle diameters at concentrations of 0.048mol/L, 0.096mol/L, 0.144mol/L and 0.192mol/L were 29.88nm, 46.74nm, 55.53nm and 59.84nm, respectively. It is thus seen that different Fe ²⁺ Average particle size of magnetic nanoparticles prepared at concentration as a function of Fe ²⁺ The concentration is increasing. Compared with Fe ²⁺ Magnetic nanoparticles formed at a concentration of 0.048mol/L, when Fe ²⁺ When the concentration is 0.096mol/L, the particle size change is large, the difference of the average particle size is 16.86nm, and Fe is continuously increased ²⁺ The change of concentration and particle size is moderate. FIG. 15 shows different Fe ²⁺ The distribution of the two-dimensional magnetic nanoparticle size at concentration is shown in FIG. 15, which shows the distribution of the magnetic nanoparticles with Fe ²⁺ The increase in concentration shows a tendency that the particle size distribution of the two-dimensional magnetic nanoparticles increases.

By the reaction of different Fe ²⁺ According to the analysis of a TEM image and a particle size distribution diagram of the two-dimensional magnetic nanoparticles under the concentration, when Fe is used ²⁺ When the concentration is 0.096mol/L, the product is in a two-dimensional sheet structure and regular in shape, and finally Fe is determined ²⁺ The concentration is 0.096 mol/L.

Example 7 Effect of precipitant concentration on morphology and size of two-dimensional magnetic nanoparticles

In the process of crystal formation, the concentration of the precipitant has certain influence on nucleation and growth, and the embodiment examines the influence of the concentration of the precipitant on the morphology and the size of the two-dimensional magnetic nanoparticles. Under the same conditions (reaction temperature of 60 ℃, stirring speed of 500rpm, reaction time of 2h, Fe) ²⁺ The dropping speed is 2.4mLmin，Fe ²⁺ Concentration of 0.096mol/L, electrostatic stabilizer concentration of 0.9mol/L), two-dimensional magnetic nanoparticles were prepared at four different precipitant concentrations (0.09mol/L, 0.18mol/L, 0.27mol/L, 0.36mol/L) by changing the precipitant concentration only during the preparation of two-dimensional magnetic nanoparticles.

Fig. 16 is a transmission electron micrograph of two-dimensional magnetic nanoparticles at different precipitant concentrations, and fig. 17 is a graph of the change in the average particle size of the two-dimensional magnetic nanoparticles with the precipitant concentration. As can be seen from fig. 16 and 17, the particle size of the two-dimensional magnetic nanoparticles shows a tendency to decrease gradually with increasing concentration of the precipitant. At a precipitant concentration of 0.09mol/L, the magnetic nanoparticles produced had a large particle size and a particle size distribution larger than those of nanoparticles under other conditions, and the two-dimensional sheet structure was observed to be constant but the spherical structure was still large in the electron micrograph (FIG. 16 (a)). When the precipitant concentration is 0.18mol/L, the particle size of the obtained magnetic nanoparticles is small, and the shape is mostly a two-dimensional sheet structure and regular (FIG. 16 (b)). When the precipitant concentration was further increased to 0.27, 0.36mol/L, the magnetic nanoparticles continued to exhibit a decreasing tendency in particle size and varied in shape, and were spherical, flaky, rod-like, and seriously agglomerated (FIGS. 16(c) and 16 (d)). As shown in FIG. 2.18, the average particle diameters at the precipitant concentrations of 0.09mol/L, 0.18mol/L, 0.27mol/L, and 0.36mol/L were 58.96nm, 46.74nm, 41.86nm, and 36.72nm, respectively. It can thus be seen that the average particle size of the magnetic nanoparticles decreases with increasing precipitant concentration. Fig. 18 is a distribution diagram of the particle size of the two-dimensional magnetic nanoparticles at different precipitant concentrations, and it can be seen from fig. 18 that the two-dimensional magnetic nanoparticle particle size distribution gradually decreases as the precipitant concentration increases.

The magnetic nanoparticles gradually decrease with increasing precipitant concentration and agglomeration becomes more and more pronounced. OH in solution when the precipitant concentration is low ^- Relatively few, only partial metal ions and OH ^- The combination forms crystal nucleus, and the rest metal ions act on the surface of the crystal to accelerate the growth rate of the nano particles. At this point, the growth rate is greater than the nucleation rate, the nanoparticles tend to grow,eventually the particle size of the nanoparticles becomes larger. Conversely, when the precipitant concentration is relatively high, a large amount of OH is present ^- And combining with metal ions to form nuclei, wherein the nucleation rate is greater than the growth rate, the nanoparticles tend to nucleate and grow slowly, and finally the particle size of the nanoparticles is reduced. In addition, as the precipitant concentration increases, the particle size of the generated magnetic nanoparticles decreases, and the specific surface energy of the magnetic nanoparticles increases, thereby causing significant agglomeration. OH in solution when the precipitant concentration is larger ^- More, with some OH groups ^- The magnetic nano particles are adsorbed on the surfaces of the magnetic nano particles, so that the surfaces of the magnetic nano particles have certain negative charges, and the possibility of magnetic nano particle agglomeration is increased due to the existence of electrostatic interaction. In the whole, when the concentration of the precipitating agent is 0.18mol/L, the particle size of the obtained magnetic nanoparticles is small, the shape of the product is mostly a two-dimensional sheet structure, the shape is regular, and the concentration of the precipitating agent is finally determined to be 0.18 mol/L.

Example 8 Effect of Electrostatic stabilizer concentration on morphology and size of two-dimensional magnetic nanoparticles

In order to clarify the effect of the concentration of the electrostatic stabilizer on the morphology and size of the magnetic nanoparticles, this example examined the effect of different electrostatic stabilizer concentrations on the morphology and size of the two-dimensional magnetic nanoparticles. Under the same conditions (reaction temperature 60 ℃, stirring speed 500rpm, reaction time 2h, Fe) ²⁺ The dropping speed is 2.4mL/min, Fe ²⁺ Concentration of 0.096mol/L, precipitant concentration of 0.9mol/L), two-dimensional magnetic nanoparticles were prepared at four different electrostatic stabilizer concentrations (0.45mol/L, 0.9mol/L, 1.35mol/L, 1.8mol/L) only by changing the electrostatic stabilizer concentration during the preparation of two-dimensional magnetic nanoparticles.

Fig. 19 is a transmission electron micrograph of the two-dimensional magnetic nanoparticles at different electrostatic stabilizer concentrations, and fig. 20 is a graph of the change in the average particle size of the two-dimensional magnetic nanoparticles with the electrostatic stabilizer concentration. As shown in fig. 19 and 20, the particle size of the two-dimensional magnetic nanoparticles shows a decrease-followed-increase change with increasing concentration of the electrostatic stabilizer. As shown in fig. 19(a), when the electrostatic stabilizer concentration is 0.45mol/L, it can be seen from the TEM image that the magnetic nanoparticles produced have a large particle size, relatively few two-dimensional sheet structures, and many spherical structures. As shown in FIG. 19(b), when the concentration of the electrostatic stabilizer is 0.9mol/L, the magnetic nanoparticles produced at this time have a large particle diameter, and are mostly two-dimensional sheet-like structures and regular in shape. When the concentration of the electrostatic stabilizer is further increased to 1.35mol/L, the particle size of the magnetic nanoparticles shows a decreasing trend, and from the appearance of the magnetic nanoparticles, only a few two-dimensional flaky particles exist, and most of the two-dimensional flaky particles are spherical particles. When the concentration reached 1.8mol/L, the magnetic nanoparticles showed an increasing tendency in particle size and were spherical in shape with almost no two-dimensional sheet structure (FIGS. 19(c) and 19 (d)). As shown in FIG. 20, the average particle diameters at the precipitant concentrations of 0.45mol/L, 0.9mol/L, 1.35mol/L, and 1.8mol/L were 48.04nm, 46.74nm, 44.55nm, and 49.64nm, respectively. It can also be seen from the change in the average particle diameter that the average particle diameter of the two-dimensional magnetic nanoparticles shows a tendency to decrease first and then increase as the concentration of the electrostatic stabilizer increases.

Fig. 21 is a distribution diagram of the particle size of the two-dimensional magnetic nanoparticles under different electrostatic stabilizer concentrations, and it can be seen from fig. 21 that the particle size distribution of the two-dimensional magnetic nanoparticles is not obviously regular with the increase of the electrostatic stabilizer concentration. This is because increasing the concentration of the electrostatic stabilizer can accelerate the nucleation and growth rate of the magnetic nanoparticles. In addition, as the electrostatic stabilizer is further increased, the shape of the nano-particles is changed, when the concentration reaches 1.35mol/L, the growth crystal face is changed to form spherical nano-particles, and when the concentration reaches 1.8mol/L, the nano-particles are almost all spherical and basically no nano-sheets are generated. This is mainly due to the fact that increasing the concentration of sodium acetate accelerates the growth rate of the two-dimensional magnetic nanoparticles, changing the growth direction of the magnetic nanoparticles, resulting in the generation of spherical nanoparticles. According to the analysis of the morphology and the particle size of the two-dimensional magnetic nanoparticles under different electrostatic stabilizer concentrations, when the electrostatic stabilizer concentration is 0.9mol/L, the generated product has regular shape and similar structure, and finally the electrostatic stabilizer concentration is determined to be 0.9 mol/L.

Example 9 two-dimensional magnetic nanoparticle phase and Crystal form Structure analysis

(1) X-ray diffraction analysis (XRD)

The above embodiments examine the influence of different reaction conditions on the morphology and size of the two-dimensional magnetic nanoparticles, and define the optimal preparation conditions. Aiming at the magnetic nanoparticles synthesized under different conditions, the magnetic nanoparticles with more sheet structures are selected for XRD test, and phase analysis is further carried out on the two-dimensional magnetic nanoparticles. Fig. 22 and 23 are XRD spectra of the two-dimensional magnetic nanoparticles at different stirring speeds and XRD spectra of the two-dimensional magnetic nanoparticles at different reaction temperatures, respectively. As shown in FIGS. 22 and 23, the XRD pattern of the two-dimensional magnetic nanoparticles mainly comprises eight characteristic diffraction peaks, and the position and intensity of each characteristic diffraction peak and Fe ₃ O ₄ The diffraction crystal faces of the two-dimensional magnetic nanoparticles corresponding to eight characteristic diffraction peaks (2 theta, 30.157 degrees, 35.521 degrees, 37.157 degrees, 43.172 degrees, 53.561 degrees, 57.098 degrees, 62.703 degrees and 74.186 degrees) are respectively (220), (311), (222), (400), (422), (511), (440) and (533), no other redundant peaks appear, the diffraction characteristic peaks of all samples are strong and sharp, and the prepared two-dimensional magnetic nanoparticles are proved to have high purity and good crystallinity.

In addition, the diffraction peaks at different temperatures and different stirring speeds can be well corresponded to the standard spectrogram by observing the spectrogram, which indicates that the magnetic nanoparticles prepared at different temperatures and different stirring speeds are all Fe ₃ O ₄ . Overall, the diffraction characteristic peak is sharper and higher with the increase of the stirring speed, and is sharpest when the stirring speed is 500rpm, while the influence of the reaction temperature on the crystallinity of the magnetic nanoparticles is not very obvious.

(2) High Resolution Transmission Electron Microscope (HRTEM)

In the synthesis of bottom-up cubic nanoparticles, the process of growing polyhedrons after nucleation is considered as an important process for initially forming nanostructures. After nucleation, the final products obtained have different morphologies under different reaction conditions. Research shows that isotropic growth makes crystal nucleusThe face centers of the six crystal faces grow concentrically and rapidly, and finally the crystal faces disappear, so that the spherical nano-particles are formed. Under specific conditions, the (111) face is limited to grow, and finally, a product with the exposed (111) face is obtained, namely the anisotropic nanosheet. In this embodiment, two-dimensional magnetic nanoparticles prepared under the optimal conditions are selected, and are characterized by HRTEM, and the growth mechanism of the nanosheets is revealed. FIG. 24 is a high resolution transmission electron micrograph of two-dimensional magnetic nanoparticles and the corresponding Fast Fourier Transform (FFT), and it can be seen from the partial enlarged view that the lattice spacing of the two-dimensional magnetic nanoparticles formed is about 0.297nm, from which the plane of the lattice fringes and Fe can be inferred ₃ O ₄ The crystal face (220) on the crystal is corresponding, and the magnetic nano-sheet synthesized by the method is further proved to be Fe ₃ O ₄ . Research shows that, in the face-centered cubic crystal,

all belong to {220} crystal system, and six crystal planes are all parallel to [111 ]]And in the same direction, with the same lattice spacing. And the included angle between adjacent crystal faces should be 60 DEG, and the direction of the electron beam can point to Fe ₃ O ₄ Of [111 ]]And in the direction, the exposed surface is the (111) surface. Meanwhile, the two-dimensional magnetic nanosheets synthesized are hexagonal with regular shapes and can be observed from both TEM results and HRTEM results, and therefore, the two-dimensional magnetic nanosheets are judged to belong to anisotropic nanoparticles.

(3) X-ray photoelectron spectroscopy (XPS)

To further determine the structure and composition of the two-dimensional magnetic nanoparticle synthetic phase, analysis was performed using an X-ray electron spectrometer. The XPS spectra of Fe2p and O1s of the two-dimensional magnetic nanoparticles are shown in fig. 25. Fe2p can be seen from the figure _3/2 And Fe2p _1/2 The binding energies of (A) and (B) were 710.5eV and 724.6eV, respectively, and the binding energy of O1s was 530.2eV, and the obtained results were in agreement with the data reported in the literature, and it was again determined that the synthesized two-dimensional magnetic nanoparticles were Fe ₃ O ₄ 。

(4) Infrared spectroscopic analysis (FT-IR)

Fig. 26 is an infrared spectrum of a two-dimensional magnetic nanoparticle. Wherein the length of the groove is 580cm ^-1 Characteristic absorption of (D) corresponds to Fe ₃ O ₄ Vibration absorption of the nano-particle Fe-O. 1605cm ^-1 3433cm bound water molecules on the surface of the product ^-1 The absorption peaks in the vicinity are characteristic absorption peaks for water and-OH. In addition to the influence of water molecules, the vibration absorption of Fe-O mainly exists in the infrared spectrogram of the two-dimensional magnetic nanoparticles, so that the infrared spectrogram also shows that the two-dimensional magnetic nanoparticles are Fe ₃ O ₄ Is a strong proof of.

Example 10 two-dimensional magnetic nanoparticle thickness analysis

As shown in fig. 27, the thickness of the two-dimensional magnetic nanoparticles was analyzed by means of atomic force microscopy. It can be seen that the surface of the synthesized two-dimensional magnetic nanoparticles is smooth. In order to investigate the thicknesses of the two-dimensional magnetic nanoparticles in different ranges, the thickness of the nanosheets on the whole surface from A to B, the thickness of the nanosheets between the line sections from C to D and the thickness of the nanosheets between the whole areas from E to F are measured respectively, and the thicknesses of the two-dimensional magnetic nanoparticles are determined by integrating the three ranges. As shown in FIG. 28, it can be seen that the distance between A and B is about 4.2nm, the distance between C and D is about 4.6nm, and the distances between the three "steps" between E and F are about 4.5nm, 4.5nm, and 4.6nm, respectively. As a whole, the thickness of the synthesized two-dimensional magnetic nanoparticles is about 4.2-4.6 nm.

A TEM image of the two-dimensional magnetic nanoparticle is shown in fig. 29, and it can be seen that the thicknesses of the two tilted nanosheets are about 4.5nm, and in summary, the thickness of the two-dimensional magnetic nanoparticle synthesized by the present invention can be basically determined to be about 4.2-4.6 nm.

AFM data were further analyzed using NanoScope Analysis software to obtain two-dimensional magnetic nanoparticle surface roughness. In a broad-range (5 μm) AFM image, the root mean square roughness Rq is about 2.18nm, and the surface roughness of the local nanosheets is examined, and the root mean square roughness Rq is about 0.28 nm. From the above surface roughness results, it can be seen that the surface of the synthesized two-dimensional magnetic nanoparticles is smooth. Fig. 30 shows an AFM 3D. From fig. 30, it can be seen that the thickness of the nanosheets is uniform, and the height difference of the nanosheets in the whole area is consistent, which proves that the two-dimensional magnetic nanoparticles have smooth surfaces and uniform thickness.

Example 11 two-dimensional magnetic nanoparticle magnetic analysis

Fig. 31 is a hysteresis loop of a two-dimensional magnetic nanoparticle, the hysteresis loop exhibiting a symmetrical structure. The hysteresis loop was tested in the range of-20 k-20 k Oe at room temperature. As can be seen from FIG. 31, the saturation magnetization (Ms) of the two-dimensional magnetic nanoparticles is 77.5emu/g, which is close to the saturation magnetization (85-95 emu/g) of the bulk magnetic material, and the saturation magnetization is lower than 85-95 emu/g because the two-dimensional magnetic nanoparticles are thin and have large specific surface area. As can be seen from the partially enlarged view, the remanent magnetization (Mr) was 11.2emu/g and the coercive force (Hc) was 106.7Oe, from which it was found that the two-dimensional magnetic nanoparticles had ferromagnetic behavior. In addition, the coercivity is high, mainly because the anisotropy of the two-dimensional magnetic nanoparticles prevents the crystals from being magnetized in directions other than the easy magnetization axis.

Fig. 32 is a photograph of a two-dimensional magnetic nanoparticle magnetic separation process, in which a small amount of two-dimensional magnetic nanoparticles are taken and sufficiently dispersed in 4mL of deionized water. Fig. 32(a) is a photograph of the two-dimensional magnetic nanoparticles dispersed in water after shaking and sonication for 1min, fig. 32(b) is a photograph after magnetic separation for 15s, and fig. 32(c) is a photograph after magnetic separation for 30 s. As can be seen from fig. 32, after the magnet is placed on the right side of the sample dispersion, the two-dimensional magnetic nanoparticles can be quickly attracted to the magnet side, so that the dispersion is clear, and when the magnet is removed, the vial is gently shaken, and the two-dimensional magnetic nanoparticles are re-dispersed in the aqueous solution, which indicates that the two-dimensional magnetic nanoparticles have good dispersibility in water. The characteristic enables the two-dimensional magnetic nanoparticles to be quickly separated from the liquid under the action of an external magnetic field, so that the recovery and the repeated use of the two-dimensional magnetic nanoparticles can be realized, and the cost is reduced.

Example 12 preparation of Janus two-dimensional magnetic nanoparticles

FIG. 33 is a schematic diagram of the synthesis of Janus two-dimensional magnetic nanoparticles.

1) The two-dimensional magnetic nanoparticles synthesized in example 1 were placed in a reaction vessel, 100mL of water was added, and then they were placed in an ultrasonic multifunction tester for 10min, after being sufficiently dispersed, they were placed in a water bath at 80 ℃ with a mechanical stirring speed of 2000 rpm. 10g of melted paraffin wax was added thereto at this stirring speed, and the above mixed solution was stirred at 80 ℃ and 2000rpm for 20 min. And cooling to room temperature, washing with absolute ethyl alcohol for multiple times to wash off the two-dimensional magnetic nanoparticles which are not adsorbed on the surface of the paraffin ball, and collecting and separating by using a magnet to obtain the paraffin ball with the two-dimensional magnetic nanoparticles adsorbed on the surface.

2) And (3) placing the collected paraffin ball into a reaction container, adding 98mL of ethanol and 2mL of aqueous solution, adjusting the pH of the dispersion to 8-9 by using 0.1mol/L aqueous solution of sodium hydroxide, adding 2mL of n-octyltriethoxysilane in batches at room temperature and a stirring speed of 500rpm, and reacting for 20 hours under the conditions. After the reaction is finished, separating by a magnet, washing with absolute ethyl alcohol for three times, then completely dissolving the paraffin spheres by cyclohexane, washing with absolute ethyl alcohol for three times again, and collecting a pure sample to obtain Fe ₃ O ₄ @OTES。

3) The Fe obtained above is added ₃ O ₄ @ OTES particles were uniformly dispersed in an aqueous ethanol solution (98 mL of ethanol, 2mL of water), and 1mL of N-aminoethyl- γ -aminopropyltrimethoxysilane was added in portions at room temperature and a stirring speed of 500rpm, and the mixture was reacted for 20 hours under these conditions. After the reaction is finished, separating by using a magnet, washing for several times by using absolute ethyl alcohol and deionized water in sequence to obtain Janus two-dimensional magnetic nanoparticles, collecting a product to be detected, and reserving for later use.

Firstly, in this embodiment, a paraffin protection method is adopted to prepare Janus two-dimensional magnetic nanoparticles. At 80 ℃, the two-dimensional magnetic nanoparticles can enable paraffin and water to form an emulsion, the two-dimensional magnetic nanoparticles are firmly adsorbed at the oil-water interface of the emulsion, and when the temperature is reduced to room temperature, the two-dimensional magnetic nanoparticles are distributed on the surface of solidified paraffin spheres. Because the two-dimensional nanoparticles are flaky particles and are not easy to rotate at an oil-water interface, the surface with a large cross section area is embedded into the paraffin spheres while the paraffin spheres are formed, so that one surface of the nanosheets is protected, the nanosheets are prevented from contacting with a modifier, the purpose of selective grafting is achieved, and the Janus two-dimensional magnetic nanoparticles are finally synthesized.

This example examines the effect of the amount of two-dimensional magnetic nanoparticles on the surface distribution of paraffin spheres and the microscopic morphology of Janus two-dimensional magnetic nanoparticles.

(1) Influence of dosage of two-dimensional magnetic nanoparticles on surface distribution of paraffin spheres

Fig. 34 is an SEM image of paraffin spheres of two-dimensional magnetic nanoparticles and paraffin. The two-dimensional magnetic nanoparticles and the paraffin spheres have strong contrast, the paraffin spheres are relatively darker in color, and the two-dimensional magnetic nanoparticles are lighter in outer layer color. As can be seen from fig. 34, a layer of two-dimensional magnetic nanoparticles is uniformly coated on the surface where the paraffin spheres are formed.

(2) Microscopic morphology analysis of Janus two-dimensional magnetic nanoparticles

FIG. 35 is a TEM image of a Janus two-dimensional magnetic nanoparticle, which is found to have a shell layer with relatively light color and a thickness of about 3.85 nm. Each particle is uniformly coated and is uniformly coated on a surface with a larger cross section area, which also proves that the two-dimensional magnetic nanoparticles are not easy to rotate at an oil-water interface.

Fig. 36 is a high resolution transmission electron micrograph of Janus two-dimensional magnetic nanoparticles and the corresponding fast fourier transform image (FFT). As can be seen from the enlarged view, the lattice spacing of the formed Janus two-dimensional magnetic nanoparticles is about 0.297nm, and the included angle of the crystal plane is 60 degrees. Positive correspondence

The included angle between every two planes in the three planes. From this, the surface of the lattice fringes and Fe can be deduced ₃ O ₄ The (220) crystal face on the crystal is corresponding. The direction of the electron beam may be directed towards Fe ₃ O ₄ Of [111 ]]And in the direction, the exposed surface is the (111) surface. The results obtained in fig. 36 are completely consistent with those of the two-dimensional magnetic nanoparticles.

Surface chemical composition analysis of two-dimensional Janus magnetic nanoparticles

Fig. 37 is an infrared spectrum of Janus two-dimensional magnetic nanoparticles. As can be seen from FIG. 37，580cm ^-1 The characteristic absorption on the left and right is the vibration absorption of Fe-O, 1465cm ^-1 Is in C-H bending vibration, 1605cm ^-1 The product surface is treated with bonded water molecule absorption bees at 2850 and 2920cm ^-1 Characteristic absorption of (D) corresponds to C-H stretching vibration, 3433cm ^-1 The absorption peaks in the vicinity are characteristic absorption peaks for water and-OH and N-H. By infrared characterization, it can be shown that the silane coupling agent has been successfully grafted onto the two-dimensional magnetic nanoparticles.

And analyzing the Janus two-dimensional magnetic nanoparticles by using Mapping element distribution and an X-ray energy spectrum, and further determining the surface chemical composition of the Janus two-dimensional magnetic nanoparticles. Fig. 38 is a diagram showing the element distribution and composition of the surface of Janus two-dimensional magnetic nanoparticles. By Mapping scanning, the content distribution of Fe, O, Si, C and N elements is inspected, and as can be seen from FIG. 38, the content distribution of C and N before and after reaction is very obvious and can be detected on Janus two-dimensional magnetic nanoparticles. Since the EDX probe depth is about 1 μm, C, N elements were detected on each face. However, it can be seen that C is circular and N can be inserted into the circular form, which is completely compatible with the synthesis and grafting sequence. In the reaction process, a cap is firstly buckled on the surface with the largest cross section area of the two-dimensional magnetic nanoparticles, and then N-aminoethyl-gamma-aminopropyltrimethoxysilane is successfully grafted on the other surface, so that the Janus two-dimensional magnetic nanoparticles are finally synthesized. And meanwhile, the N content change of local point positions is inspected through an X-ray energy spectrometer, the N content of the Janus two-dimensional magnetic nanoparticles is 5.95 percent respectively and is far higher than that of the two-dimensional magnetic nanoparticles, and therefore, the fact that the N-aminoethyl-gamma-aminopropyltrimethoxysilane is successfully grafted to the two-dimensional magnetic nanoparticles can be inferred. This is also a strong corroboration to the infrared test results. In conclusion, the success of the preparation of Janus two-dimensional magnetic nanoparticles can be proved.

Contact angle analysis of three, Janus two-dimensional magnetic nanoparticles

The synthesized Janus two-dimensional magnetic nanoparticle dispersion liquid is injected into a toluene/water system, and after shaking, the phenomenon that emulsion liquid drops are rapidly combined occurs, so that the nanosheets are spontaneously accumulated, and an elastic interfacial film is formed. The amphipathy and the amphipathy of the synthesized Janus two-dimensional magnetic nanoparticles are proved through the measurement of the contact angle of the water phase. Fig. 39 is a photograph showing the water contact angle of Janus two-dimensional magnetic nanoparticles, and as can be seen from fig. 39, one side is hydrophilic and the contact angle is about 45 °, and the other side is hydrophobic and the contact angle is about 117 °. The two-sided wettability of the Janus two-dimensional magnetic nanoparticles is significantly different, indicating that each side of the Janus two-dimensional magnetic nanoparticles has a different chemical group.

Interfacial properties of four, Janus two-dimensional magnetic nanoparticles

The interfacial tension of Janus two-dimensional magnetic nanoparticles is shown in fig. 40. It can be seen that the interfacial tension of toluene and water is about 31.1mN/m, upon addition of Fe ₃ O ₄ After that, the interfacial tension was decreased to about 25.2mN/m, indicating that Fe ₃ O ₄ There are some effects on the oil-water interfacial tension. For toluene/water/Janus Fe ₃ O ₄ Systems, when toluene droplets are formed, following Janus Fe ₃ O ₄ The instantaneous assembly at the interface causes a rapid decrease in interfacial tension, and then the rate of decrease in interfacial tension is slowed, and finally the interfacial tension approaches an equilibrium value of 15.1 mN/m. Due to Janus Fe ₃ O ₄ Adsorption at the oil/water interface and thus more effective reduction of the oil/water interfacial tension.

Janus two-dimensional magnetic nanoparticles are dripped into oil/water, and the influence of the Janus two-dimensional magnetic nanoparticles on an oil/water interface is analyzed. To exclude the influence of gravity, toluene with a density less than that of water and dichloromethane with a density greater than that of water were respectively selected as oil phases, and Sudan III was used to dye the oil phases for observation. As shown in fig. 41(a), 41(b), and 41(c), the Janus two-dimensional nanoparticles spontaneously aggregated at the toluene/water interface (fig. 41(b)) after dropping into the toluene/water interface, and slight wall climbing phenomenon was observed. After shaking gently, the mixture stabilized after shaking, a layer of Janus Fe ₃ O ₄ The film of nanoparticles quickly climbs up the inner wall of the container. After equilibration, Janus Fe ₃ O ₄ A flat and uniform interfacial film is formed at the toluene/water interface, and simultaneously the oil-water interfacial tension is reduced, so that the concave liquid level of toluene and water is changed into a flat liquid level. The main reason is Janus Fe ₃ O ₄ The amphiphilicity and the bilaterality of (A) reduce the interfacial tension, so that the materials can be spontaneously accumulated at a toluene/water interface to form an interfacial film. With Janus Fe ₃ O ₄ The increase in interfacial concentration increases the surface pressure at the toluene/water interface, and the corresponding diffusion pressure pushes the toluene/water interface up to the bottle wall, forming a climbing membrane (fig. 41 (c)). Further examining Janus Fe as shown in FIG. 41(d), FIG. 41(e) and FIG. 41(f) ₃ O ₄ Change the Janus Fe in the interface of dichloromethane/water ₃ O ₄ Janus Fe after nanoparticles were dropped into the dichloromethane/water interface ₃ O ₄ Aggregation at the toluene/water interface (FIG. 41 (e)). After stabilization by gentle shaking, a layer of Janus Fe ₃ O ₄ The film of nanoparticles was wrapped outside the dichloromethane, while some of the film quickly climbed onto the inner wall of the vessel. It is noteworthy that the interfacial film formed at this time is very uniform and continuous, compared to the hydrophobically modified two-dimensional magnetic nanoparticles, again due to Janus Fe ₃ O ₄ The amphiphilicity and the amphiphilicity of (1) (FIG. 41 (f)).

Further, the strength and deformation characteristics of the formed interface film were examined, and the results are shown in fig. 42. As can be seen from fig. 42(a), the interfacial film is deformed but not broken after the capillary is inserted, thereby illustrating that the interfacial film has certain elasticity and strength. Fig. 42(b) shows that the interface film is deformed by the attraction of the magnet, and the interface film is stretched downward by the attraction of the magnet, and the interface film returns to its original shape when the magnet is removed (fig. 42 (c)). Therefore, the interfacial film formed by the Janus two-dimensional magnetic nanoparticles has certain strength and certain elasticity. Meanwhile, an interface film formed by the Janus two-dimensional magnetic nanoparticles on an oil-water interface still has magnetic responsiveness.

Magnetic analysis of five, Janus two-dimensional magnetic nanoparticles

Fig. 43 is a hysteresis loop of Janus two-dimensional magnetic nanoparticles. As can be seen from FIG. 43, when the magnetic field strength reached 20000Oe, Janus Fe was subjected to the grafting reaction ₃ O ₄ The saturation magnetization (Ms) of (1) was 48.9 emu/g. After the two-time reaction, the silane coupling agent is uniformly coated on the surface of the two-dimensional magnetic nanoparticle, resulting in a decrease in saturation magnetization (Ms), which can also be demonstratedThe invention successfully grafts the silane coupling agent on the magnetic nano-particles. Although Janus Fe ₃ O ₄ The magnetization intensity of the nano-sheets is reduced, but the nano-sheets still have strong magnetism. As can be seen from the enlarged view, the residual magnetization (Mr) of the Janus two-dimensional magnetic nanoparticle is 6.0emu/g, and the coercive force (Hc) is 56.5Oe, which are both reduced, and are considered to be caused by the surface grafting of the silane coupling agent.

Fig. 44 is a photograph of a magnetic separation process of Janus two-dimensional magnetic nanoparticles, wherein a small amount of Janus two-dimensional magnetic nanoparticles are taken and fully dispersed in 4mL of deionized water. Fig. 44(a) is a photograph of the magnetic nanoparticles dispersed in water after shaking and sonication for 1min, fig. 44(b) is a photograph after magnetic separation for 30s, and fig. 44(c) is a photograph after magnetic separation for 60 s. It can be seen from fig. 44 that after the magnet is placed on the right side of the sample dispersion, the magnetic nanoparticles can be attracted to the magnet side quickly, thereby clarifying the dispersion. Janus Fe after 60s magnetic separation ₃ O ₄ The dispersion became clear. In conclusion, the Janus two-dimensional magnetic nanoparticles prepared by the invention have good magnetic responsiveness. The characteristic enables the Janus two-dimensional magnetic nanoparticles to be rapidly separated from the liquid under the action of an external magnetic field.

Example 13 preparation of magnetic Pickering emulsion

The method comprises the steps of preparing Pickering emulsion from the Janus two-dimensional magnetic nanoparticles prepared in the embodiment 12, weighing 0.02g of Janus two-dimensional magnetic nanoparticles, dispersing the Janus two-dimensional magnetic nanoparticles into 2mL of dodecane and 2mL of deionized water, placing the mixture into an ultrasonic cleaner, carrying out ultrasonic treatment for 25min to form black emulsion containing magnetic nanosheets, changing the mass fraction and the oil phase (normal hexane, dichloromethane and butyl butyrate) of the nanoparticles, and forming the magnetic Pickering emulsion by the same method.

Investigation of Janus two-dimensional magnetic nanoparticle stable emulsions:

(1) pickering emulsion formed by Janus two-dimensional magnetic nanoparticles with different mass fractions

Fig. 45 is an optical microscope image of Pickering emulsion prepared from different mass fractions of Janus two-dimensional magnetic nanoparticles and dodecane. As can be seen from fig. 45, under the conditions of 1:1 oil-water ratio and 4mL total oil-water volume, the Janus two-dimensional magnetic nanoparticles can form an emulsion with dodecane. Meanwhile, as can also be seen from fig. 45, as the mass fraction of the Janus two-dimensional magnetic nanoparticles gradually increases, the droplets forming the emulsion have a gradually decreasing tendency. Mainly because the Janus two-dimensional magnetic nanoparticles are similar to a small molecular surfactant when being used as an emulsifier, the size of the formed emulsion liquid drop can be adjusted through the dosage of the Janus two-dimensional magnetic nanoparticles. When the mass fraction of the Janus two-dimensional magnetic nanoparticles is 0.5 wt%, the Janus two-dimensional magnetic nanoparticles can form stable emulsion with dodecane, and the size distribution of emulsion droplets is uniform.

(2) Pickering emulsion formed by Janus two-dimensional magnetic nanoparticles and different oil phases

Fig. 46 is an optical microscopy image of Pickering emulsions prepared with 0.5 wt% Janus two-dimensional magnetic nanoparticles and different oil phases. As can be seen from fig. 46, the Janus two-dimensional magnetic nanoparticles can form a stable emulsion with dodecane and n-hexane having weak polarity, and can also form an emulsion with dichloromethane having slightly strong polarity and even butyl butyrate having strong polarity. On the whole, the droplet size distribution of the Pickering emulsion formed by the Janus two-dimensional magnetic nanoparticles and the oil phases is uniform and stable. This corresponds to the result in example 12 of the Janus two-dimensional magnetic nanoparticles forming a uniform and continuous interfacial film with dichloromethane, especially from an emulsion with dichloromethane. The Janus two-dimensional magnetic nanoparticles can form efficient and stable Pickering emulsion mainly caused by the amphiphilicity and the amphiphilicity of the Janus two-dimensional magnetic nanoparticles.

Claims

1. A preparation method of Janus two-dimensional magnetic nanoparticles comprises the following steps:

s2, dispersing the paraffin spheres with the two-dimensional magnetic nanoparticles adsorbed on the surfaces in an ethanol water solution, regulating the pH value to 8-9, adding n-octyl triethoxysilane for reaction, separating by using a magnet after the reaction is finished, and dissolving to remove the paraffin spheres to obtain Fe ₃ O ₄ @ OTES particles;

s3, mixing the Fe ₃ O ₄ Dispersing the @ OTES particles in an ethanol water solution, adding N-aminoethyl-gamma-aminopropyltrimethoxysilane for reaction, and separating by using a magnet after the reaction is finished to obtain the Janus two-dimensional magnetic nanoparticles;

the two-dimensional magnetic nanoparticles are prepared according to a method comprising the following steps:

dropwise adding an aqueous solution of ferrous sulfate heptahydrate into an aqueous solution of sodium hydroxide and sodium acetate, and reacting under the condition of stirring; and after the reaction is finished, collecting and separating by using a magnet to obtain the two-dimensional magnetic nanoparticles.

2. The method of claim 1, wherein: in step S1, stirring at 20-40 ℃;

in step S2, adjusting the pH value with sodium hydroxide aqueous solution;

the dosage of the n-octyl triethoxysilane is as follows: 1g of 0.5-2 mL of the n-octyltriethoxysilane;

the reaction temperature is 20-40 ℃, and the reaction time is 10-20 h.

3. The production method according to claim 1 or 2, characterized in that: in step S3, the dosage of N-aminoethyl- γ -aminopropyltrimethoxysilane is: 0.25-1 mL of the N-aminoethyl-gamma-aminopropyltrimethoxysilane;

the reaction temperature is 20-40 ℃, and the reaction time is 10-20 h.

4. The production method according to any one of claims 1 to 3, characterized in that: in the step SA, the reaction temperature is 50-60 ℃;

under the condition of water bath;

the stirring speed is 400-500 rpm.

5. The production method according to any one of claims 1 to 4, characterized in that: the reaction time is 2-3 h;

the dropping speed of the aqueous solution of the ferrous sulfate heptahydrate is 2-2.4 mL/min.

6. The production method according to any one of claims 1 to 5, characterized in that: in the aqueous solution of the ferrous sulfate heptahydrate, the molar concentration of the ferrous sulfate heptahydrate is 0.096-0.144 mol/L;

in the aqueous solution of sodium hydroxide and sodium acetate, the molar concentration of the sodium hydroxide is 0.18-0.27 mol/L, and the molar concentration of the sodium acetate is 0.9-1.35 mol/L.

7. Janus two-dimensional magnetic nanoparticles prepared by the method of any one of claims 1-6.

8. The use of the Janus two-dimensional magnetic nanoparticles of claim 7 in the preparation of Pickering emulsions, interfacial catalysis, and petroleum industry.

9. A preparation method of Pickering emulsion comprises the following steps:

dispersing the Janus two-dimensional magnetic nanoparticles as defined in claim 7 in a mixed system of an oil phase and a water phase, and obtaining the Janus two-dimensional magnetic nanoparticles by dispersion;

the oil phase is dodecane, n-hexane, dichloromethane or butyl butyrate;

the volume ratio of the oil phase to the water phase is 1: 1-2;

10. A Pickering emulsion made by the process of claim 9.