CN114833337A - Preparation method of spherical gallium-magnesium Janes particles - Google Patents

Preparation method of spherical gallium-magnesium Janes particles Download PDF

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Publication number
CN114833337A
CN114833337A CN202210364959.8A CN202210364959A CN114833337A CN 114833337 A CN114833337 A CN 114833337A CN 202210364959 A CN202210364959 A CN 202210364959A CN 114833337 A CN114833337 A CN 114833337A
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gallium
magnesium
particles
janes
aluminum
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CN114833337B (en
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胡那日苏
迟航
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Harbin Medical University
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Harbin Medical University
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/26Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/06Aluminium; Calcium; Magnesium; Compounds thereof
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • C23C14/16Metallic material, boron or silicon on metallic substrates or on substrates of boron or silicon
    • C23C14/165Metallic material, boron or silicon on metallic substrates or on substrates of boron or silicon by cathodic sputtering
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/223Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating specially adapted for coating particles
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/36Hydrogen production from non-carbon containing sources, e.g. by water electrolysis

Abstract

A preparation method of spherical gallium-magnesium Janes particles relates to the technical field of metal preparation. Aiming at solving the problems that the existing gallium-aluminum and gallium-zinc Janes micromotors can be used as bactericides, but the gallium-aluminum micromotors contain a large amount of aluminum ions, and the aluminum is extremely toxic; if the gallium-zinc Janes micromotor is used as a bactericide, the action can be generated only in an acidic environment; the two kinds of metal particles are harmful to human bodies when used. The gallium-magnesium particles can be manufactured by adopting the preparation method, the aluminum layer is deposited on the surface of the exposed magnesium ball by utilizing vacuum sputtering equipment in the second step, the aluminum layer is used as an adhesion layer, the surface of the magnesium ball can be coated with a layer of gallium, and the ratio of aluminum ions in the aluminum layer is small and can be ignored; therefore, the gallium-magnesium particles are nontoxic, can be used as a bactericide, react with water to generate a sterilizing effect when in use, do not need to be used in a specific environment, and do not cause harm to human bodies. The invention is applicable to the field of metal preparation.

Description

Preparation method of spherical gallium-magnesium Janes particles
Technical Field
The invention relates to the technical field of metal preparation, in particular to a preparation method of spherical gallium-magnesium Janes particles.
Background
Magnesium has wide distribution, active chemical property, good biocompatibility and easy acquisition. Janes structure, which can make the particle generate hydrogen bubbles on one side to make it have motion characteristics, the generated water-driven microparticles can effectively move in different biological media, and has considerable prospect in different biomedical or industrial applications.
Gallium is a liquid metal with a low melting point and a high boiling point. So far, the successful synthesis of gallium aluminum and gallium zinc Janes micro-motors has been studied, mainly based on the embrittlement characteristics of liquid metal. Although gallium aluminum Janes micromotors can utilize the reaction of aluminum nuclei with water to produce the driving force, excess aluminum can produce some toxicity: chemical propellants are required for gallium zinc Janes micromotors to generate driving forces. Both types of micromotors have certain limitations in their application. The magnesium particles can directly use water as fuel to generate hydrogen bubbles to propel the power thereof, thereby eliminating the requirement for common toxic fuels.
In summary, the existing gallium-aluminum and gallium-zinc Janes micromotors can be used as bactericides, but the gallium-aluminum micromotors contain a large amount of aluminum ions, and excessive aluminum generated in use can generate certain toxicity; if the gallium-zinc Janes micromotor is used as a bactericide, the action can be generated only in an acidic environment; both kinds of metal particles are harmful to human body.
Disclosure of Invention
The invention aims to solve the problems that the existing gallium-aluminum and gallium-zinc Janes micromotors can be used as bactericides, but the gallium-aluminum micromotors contain a large amount of aluminum ions, and excessive aluminum generated in use can generate certain toxicity; if the gallium-zinc Janes micromotor is used as a bactericide, the action can be generated only in an acidic environment; the two kinds of metal particles are harmful to human body, and a preparation method of spherical gallium-magnesium Janes particles is provided.
The invention relates to a preparation method of spherical gallium-magnesium Janes particles, which comprises the following steps:
step one, dispersing magnesium metal particles on a glass slide to form a particle monolayer;
depositing an aluminum layer on the surface of the exposed magnesium ball by using vacuum sputtering equipment, wherein the deposition process is carried out at room temperature;
dispersing liquid metal gallium on another glass sheet in the same mass; the two slides were then stored under compression at 80 ℃ for 2 hours, cooled to room temperature (25 ℃), and the slides were carefully separated;
step four, stripping gallium and magnesium Janes particles from the glass slide in the step three by using an ultrasonic method, and then collecting by centrifugation;
step five, alternately washing the centrifugally collected particles for 3-5 times by using absolute ethyl alcohol and acetone solution;
Sixthly, observing the morphology of the micron particles through analysis of a Scanning Electron Microscope (SEM) and an energy dispersive X-ray spectrum (EDX);
further, the particle size of the magnesium metal particles in the first step is 25 +/-5 μm;
further, the time for carrying out precipitation in the second step is kept within 120 s;
further, the pressure of aluminum in the vacuum sputtering equipment in the second step is 2.5 mTor;
further, the direct current power of the vacuum sputtering equipment in the second step is 200W;
further, the purity of the vacuum sputtering aluminum target of the vacuum sputtering equipment in the second step is 99.999 percent;
furthermore, in the third step, the metal gallium needs to be preheated to 40 ℃;
further, in the fifth step, the collected particles are washed for 4 times by using absolute ethyl alcohol and acetone solution alternately;
compared with the prior art, the invention has the following beneficial effects:
the invention overcomes the defects of the prior art, the gallium-magnesium Janes particles can be manufactured by adopting the preparation method, the aluminum layer is deposited on the surface of the exposed magnesium ball by utilizing vacuum sputtering equipment in the step two, the aluminum layer is used as an adhesion layer, the surface of the magnesium ball can be coated with a layer of gallium, and the proportion of aluminum ions in the aluminum layer is small and can be ignored; therefore, the gallium-magnesium Janes particles are non-toxic, can be used as a bactericide, can react with water to generate a sterilizing effect when used, are not required to be used under a specific environment, and cannot cause harm to a human body.
Drawings
FIG. 1 is a Scanning Electron Microscope (SEM) of spherical gallium and magnesium Janes particles with a single diameter of 25 μm prepared by the method for preparing spherical gallium and magnesium Janes particles of the present invention;
FIG. 2 is an energy dispersive x-ray spectroscopy (EDX) of a spherical gallium and magnesium Janes particle having a diameter of 25 μm prepared by the method for preparing a spherical gallium and magnesium Janes particle of the present invention;
FIG. 3 is a Scanning Electron Microscope (SEM) of a plurality of spherical gallium and magnesium Janes particles prepared by the method for preparing spherical gallium and magnesium Janes particles of the present invention;
FIG. 4 is an energy dispersive x-ray spectroscopy (EDX) of a plurality of spherical gallium and magnesium Janes particles prepared by the method for preparing spherical gallium and magnesium Janes particles of the present invention;
FIG. 5 is a particle size histogram of spherical GaMgJanes particles prepared by the method of the present invention;
wherein Panel A of FIG. 4 shows the detection of the signal of magnesium in a plurality of magnesium gallium particles; b, detecting the signal of aluminum element in a plurality of gallium-magnesium particles; the diagram C is the detection of gallium element signals in a plurality of gallium magnesium particles, and the detection signals of the gallium element signals are strongest at the same position of aluminum element; and the D picture is a layered image of gallium-magnesium particle gallium-magnesium-aluminum elements of a plurality of Janus structures.
Detailed Description
The first embodiment is as follows: referring to fig. 1 to 5, the method for preparing spherical gallium-magnesium Janes microparticles according to the present embodiment is described as follows:
step one, dispersing magnesium metal particles on a glass slide to form a particle monolayer;
depositing an aluminum layer on the surface of the exposed magnesium ball by using vacuum sputtering equipment, wherein the deposition process is carried out at room temperature;
dispersing liquid metal gallium on another glass sheet in the same mass; the two slides were then stored under compression at 80 ℃ for 2 hours, cooled to room temperature (25 ℃), and the slides were carefully separated;
step four, stripping gallium and magnesium Janes particles from the glass slide in the step three by using an ultrasonic method, and then collecting by centrifugation;
step five, alternately washing the centrifugally collected particles for 3-5 times by using absolute ethyl alcohol and acetone solution;
sixthly, observing the morphology of the micron particles through analysis of a Scanning Electron Microscope (SEM) and an energy dispersive X-ray spectrum (EDX);
according to the specific embodiment, a deposition method is combined with a micro-contact method, a complex process is not needed, the synthesis steps are simple, and spherical gallium and magnesium Janes particles with the required particle size are directly obtained; in the second step, vacuum sputtering equipment is utilized to deposit an aluminum layer on the surface of the exposed magnesium ball, the aluminum layer is used as an adhesion layer, the surface of the magnesium ball can be coated with a layer of gallium, and the proportion of aluminum ions in the aluminum layer is small and can be ignored; therefore, the gallium-magnesium Janes particles are non-toxic, can be used as a bactericide, can react with water to generate a sterilizing effect when used, are not required to be used under a specific environment, and cannot cause harm to a human body.
The second embodiment is as follows: the present embodiment will be described with reference to fig. 1 to 5, which is a further limitation of the preparation method according to the first embodiment, and the preparation method of spherical gallium magnesium Janes fine particles according to the present embodiment, in which the particle size of the magnesium metal fine particles in the first step is 25 ± 5 μm.
The third concrete implementation mode: the present embodiment is described with reference to fig. 1 to fig. 5, and the present embodiment is a further limitation of the preparation method according to the first embodiment, in the preparation method of spherical gallium magnesium Janes fine particles according to the present embodiment, the time for performing precipitation in the second step is kept within 120 s;
in the specific embodiment, the time for precipitation in the second step is kept within 120s, the deposited aluminum layer is used as an adhesion layer, the minimum value is taken within the range of ensuring the effect, the gallium can penetrate through the crystal boundary of the aluminum, and the 120s precipitation effect is better after comparison of multiple groups of experimental results.
The fourth concrete implementation mode: the present embodiment is described with reference to fig. 1 to 5, and the present embodiment is a further limitation of the preparation method according to the first embodiment, in the preparation method of spherical gallium magnesium Janes particles according to the present embodiment, the pressure of aluminum in the vacuum sputtering apparatus in the second step is 2.5 mTor;
In this embodiment, the pressure of aluminum in the vacuum sputtering apparatus in the second step is set to 2.5mTor, and the pressure of aluminum is set to 2.5mTor, so that aluminum can be uniformly attached to the surface of the magnesium particles.
The fifth concrete implementation mode: the present embodiment is described with reference to fig. 1 to 5, and the present embodiment is a further limitation to the preparation method according to the first or fourth embodiment, and the method for preparing spherical gallium magnesium Janes particles according to the present embodiment is characterized in that the dc power of the vacuum sputtering apparatus in the second step is 200W;
the sixth specific implementation mode: the present embodiment is described with reference to fig. 1 to 5, and the present embodiment is a further limitation to the preparation method according to the first or fourth embodiment, and the method for preparing spherical gallium magnesium Janes microparticles according to the present embodiment has a purity of 99.999% of the vacuum sputtered aluminum target of the vacuum sputtering apparatus in the second step;
the seventh embodiment: the present embodiment is described with reference to fig. 1 to fig. 5, and the present embodiment is a further limitation to the preparation method of the first embodiment, and the preparation method of spherical gallium-magnesium Janes particles of the present embodiment requires preheating gallium metal to 40 ℃ in the third step;
The specific implementation mode is eight: the present embodiment is described with reference to fig. 1 to 5, and the present embodiment is a further limitation of the preparation method according to the first embodiment, and the preparation method of spherical gallium magnesium Janes microparticles according to the present embodiment, in the fifth step, the collected particles are washed with anhydrous ethanol and acetone solution for 4 times alternately;
in the specific embodiment, the collected particles are alternately washed 4 times by using absolute ethyl alcohol and isopropanol solution in the step five, organic impurities except the metal particles are removed by using acetone, and finally the particles are stored in the absolute ethyl alcohol.

Claims (8)

1. A preparation method of spherical gallium-magnesium Janes particles is characterized by comprising the following steps: the specific method comprises the following steps:
dispersing magnesium metal particles on a glass slide to form a particle single layer;
depositing an aluminum layer on the surface of the exposed magnesium ball by using vacuum sputtering equipment, wherein the deposition process is carried out at room temperature;
dispersing liquid metal gallium on another glass sheet in the same mass; pressing the two slides together at 80 deg.C for 2 hr, cooling to room temperature of 25 deg.C, and separating the slides;
step four, stripping gallium and magnesium Janes particles from the glass slide in the step three by using an ultrasonic method, and then collecting by centrifugation;
Step five, washing the centrifugally collected particles for 3-5 times by using absolute ethyl alcohol and acetone solution alternately;
and sixthly, observing the morphology of the micron particles through scanning electron microscope SEM and energy dispersive x-ray spectroscopy EDX analysis.
2. The method for preparing spherical gallium-magnesium Janes particles as claimed in claim 1, wherein: the particle size of the magnesium metal particles in the first step is 25 +/-5 microns.
3. The method for preparing spherical gallium-magnesium Janes particles as claimed in claim 1, wherein: the time for carrying out precipitation in the second step is kept within 120 s.
4. The method for preparing spherical gallium-magnesium Janes particles as claimed in claim 1, wherein: and the pressure of the aluminum in the vacuum sputtering equipment in the second step is 2.5 mTor.
5. The method for preparing spherical gallium-magnesium Janes microparticles according to claim 1 or 4, wherein: and the direct current power of the vacuum sputtering equipment in the second step is 200W.
6. The method for preparing spherical gallium-magnesium Janes microparticles according to claim 1 or 4, wherein: the purity of the vacuum sputtering aluminum target of the vacuum sputtering equipment in the step two is 99.999 percent.
7. The method for preparing spherical gallium-magnesium Janes particles as claimed in claim 1, wherein: in the third step, the metallic gallium needs to be preheated to 40 ℃.
8. The method for preparing spherical gallium-magnesium Janes particles as claimed in claim 1, wherein: in the fifth step, the collected particles are washed by using absolute ethyl alcohol and acetone solution for 4 times alternately.
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