Porous zinc and preparation and application thereof
Technical Field
The invention belongs to the research field of nano porous materials, and particularly relates to porous nano zinc and preparation and application thereof.
Background
The porous metal is a material with larger specific surface area than a bulk material, wherein the nano-porous material has the unique physical and chemical properties of the nano-material due to the nano-size, and has great application prospects in catalysis, sensing, surface-enhanced Raman scattering and the like at present. At present, the nano porous metal material is mainly an inert metal nano porous material. The preparation of more active metal nanoporous materials has not been reported.
The prior art can only prepare porous structures of relatively inert metals and cannot prepare porous structures of metals as active as zinc. The porous structure of active metal zinc, namely nano porous zinc, is prepared by the method.
Disclosure of Invention
The invention solves the problems: overcomes the defects of the prior art, provides porous zinc and preparation and application thereof, and has good bacteriostatic function.
In order to overcome the problems in the prior art, the invention aims to provide nano-porous zinc and preparation and application thereof.
In order to achieve the above objects and other related objects, the present invention adopts the following technical solutions:
in a first aspect of the invention, a preparation method of nano-porous zinc is provided, which comprises the following steps:
(1) mixing zinc and magnesium, and heating to a molten state to obtain a zinc-magnesium alloy; then cooling to room temperature;
(2) and (2) removing magnesium in the zinc-magnesium alloy obtained in the step (1) by adopting electrochemical corrosion, cutting the zinc-magnesium alloy, placing the zinc-magnesium alloy in a ethylene carbonate solution of lithium perchlorate, corroding by adopting a constant potential electrochemical corrosion method, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and the zinc-magnesium alloy as a working electrode, applying voltage on the zinc-magnesium alloy electrode, and finishing the corrosion when the corrosion current is lower than 50 mu A. (ii) a Then cleaning and drying the nano-porous zinc.
Preferably, in the step (1), the atomic ratio of zinc and magnesium is (15-50): (85-50).
Preferably, in the step (1), the atomic ratio of zinc and magnesium is (25-35): (75-65).
Preferably, in the step (1), the heating temperature is in the range of 600 ℃ to 800 ℃; the heating time is 1-10 h.
Preferably, in the step (1), the heating temperature is in the range of 600 ℃ to 800 ℃; the heating time is 3-6 h.
Preferably, in the step (1), the cooling speed is 1-35 ℃/min.
Preferably, in the step (1), the cooling speed is 10 ℃/min to 25 ℃/min.
Preferably, in the step (2), the electrolyte is lithium perchlorate, and the electrochemical corrosion voltage is-1.2V to-1.4V.
Preferably, in the step (2), the concentration of the lithium perchlorate in the ethylene carbonate solution is in the range of 0.05M to 0.5M.
Preferably, in the step (2), the concentration of the lithium perchlorate in the ethylene carbonate solution is in the range of 0.3M to 0.5M.
Preferably, in the step (2), distilled water and ethanol are used for washing.
In a second aspect of the invention, there is provided a nanoporous zinc obtained by the aforementioned preparation method. Preferably, the copper-based composite material comprises a continuous nanometer-sized copper framework and a continuous nanometer-sized pore canal, wherein the nanometer-sized pore canal is communicated with each other, the nanometer-sized copper framework is communicated with each other, and the nanometer-sized copper framework and the nanometer-sized pore canal are mutually interpenetrated.
In a third aspect of the invention, the application of the nano-porous zinc in the bacteriostatic field is provided.
Compared with the prior art, the invention has the following beneficial effects: the invention uses electrochemical corrosion method to prepare active metal zinc porous material, namely nano porous zinc, which is block-shaped by macroscopic observation; the microscopic structure is like coral observed by an electronic scanning microscope and comprises a continuous nanometer copper framework and a continuous nanometer pore canal, the nanometer pore canal is communicated with each other, the nanometer copper framework is communicated with each other, and the nanometer copper framework and the nanometer pore canal are mutually interpenetrated.
Drawings
FIG. 1 is a scanning electron micrograph of the internal structure of the prepared nanoporous zinc of example 1 of the present invention;
FIG. 2 is a comparison diagram of an embodiment of the present invention; as shown in FIG. 2, the tube No. 4 is a control group, and it can be found that the tube Nos. 1, 2 and 3 have obvious bacteriostatic effect on Escherichia coli with porous zinc contents of 50 μ g, 100 μ g and 150 μ g, respectively, while the bacteria in the control group reproduce normally.
Detailed Description
Before the present embodiments are further described, it is to be understood that the scope of the invention is not limited to the particular embodiments described below; it is also to be understood that the terminology used in the examples is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention. Test methods in which specific conditions are not specified in the following examples are generally carried out under conventional conditions or under conditions recommended by the respective manufacturers.
When numerical ranges are given in the examples, it is understood that both endpoints of each of the numerical ranges and any value therebetween can be selected unless the invention otherwise indicated. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In addition to the specific methods, devices, and materials used in the examples, any methods, devices, and materials similar or equivalent to those described in the examples may be used in the practice of the invention in addition to the specific methods, devices, and materials used in the examples, in keeping with the knowledge of one skilled in the art and with the description of the invention.
Example 1
(1) According to the proportion that 15 percent of zinc and the balance of magnesium are mixed according to atomic percentage, the temperature is raised to 600 ℃ and kept for 4 hours. After 4 hours, the temperature was lowered to room temperature at 1 ℃ per minute.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.05M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.2V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
The nano-porous zinc prepared by the embodiment is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-zinc framework and a continuous nano-pore canal.
Example 2
(1) According to the proportion that 30 percent of the atomic percent is zinc and the rest is magnesium, the temperature is increased to 800 ℃, and the temperature is kept for 5 hours. After 5 hours, the temperature was reduced to room temperature at 15 ℃ per minute.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.5M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.4V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
The nano-porous zinc prepared by the embodiment of the invention is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-zinc framework and a continuous nano-pore canal.
Example 3
(1) The temperature was raised to 700 c at 50 atomic percent zinc, the remainder being magnesium, and held at that temperature for 3 hours. After 3 hours, the temperature was reduced to room temperature at 12 ℃ per minute.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.35M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.3V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
As shown in fig. 1, the nano-porous zinc prepared by the present embodiment of the invention is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-sized zinc skeleton and a continuous nano-sized pore channel.
Example 4
(1) The temperature was raised to 780 ℃ at 25 atomic percent zinc and the balance magnesium and held at this temperature for 2 hours. After 2 hours, the temperature was reduced to room temperature at 2 ℃ per minute.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.25M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.3V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
The nano-porous zinc prepared by the embodiment is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-zinc framework and a continuous nano-pore canal.
Example 5
(1) The temperature was raised to 950 ℃ at 40 atomic percent zinc, the balance magnesium, and held at this temperature for 5 hours. After 5 hours, the temperature was reduced to room temperature at 20 ℃ per minute.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.2M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.25V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
The nano-porous zinc prepared by the embodiment of the invention is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-zinc framework and a continuous nano-pore canal.
Example 6
(1) The temperature was raised to 650 ℃ at 35 atomic percent zinc, the remainder being magnesium, and held at this temperature for 6 hours. After 6 hours, the temperature was reduced to 7 ℃ per minute and the temperature was reduced to room temperature.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.15M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.35V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
The nano-porous zinc prepared by the embodiment of the invention is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-zinc framework and a continuous nano-pore canal.
Example 7
(1) The temperature was raised to 730 ℃ at 45 atomic% zinc and the remainder magnesium, and held at this temperature for 1 hour. After 1 hour, the temperature was reduced to 25 ℃ per minute and the temperature was reduced to room temperature.
(2) Cutting an alloy cube of 2mm x 2mm from the smelted alloy, placing the alloy cube in a lithium perchlorate ethylene carbonate solution with the concentration of 0.1M, adopting a constant potential electrochemical corrosion method to carry out corrosion, taking Ag/AgCl as a reference electrode, a platinum electrode as a counter electrode and a zinc-magnesium alloy as a working electrode, applying a voltage of-1.27V to the zinc-magnesium alloy electrode, and when the corrosion current is lower than 50 muA, judging that the corrosion is finished.
The nano-porous zinc prepared by the embodiment of the invention is observed by a scanning electron microscope, and the microstructure of the nano-porous zinc is like coral, and comprises a continuous nano-zinc framework and a continuous nano-pore canal.
Example 8
(1) 100 μ L of sterilized normal saline solution is added into EP tube 1.5m L, labeled as 1, 2, 3, 4, 50 μ g, 100 μ g, 150 μ g porous zinc is added into tubes 1, 2, 3, respectively, and ultrasonic dispersion is performed.
(2) Taking 10 μ L of 107CFU/m L Escherichia coli is added into the above four EP tubes respectively, and placed into a shaker at 37 deg.C for 25min, 10 μ L of the mixed solution is added into 990 μ L of physiological saline, and shaken well.
(3) From the above (2), 100. mu.L of the solution was uniformly applied to a plate. Photographs were taken after 2 days of growth.
As shown in FIG. 2, tube No. 4 is a control group, and it can be found that tubes No. 1, 2 and 3 have obvious bacteriostatic effect on Escherichia coli, while the bacteria in the control group reproduce normally.
While the invention has been described with respect to a preferred embodiment, it will be understood by those skilled in the art that the foregoing and other changes, omissions and deviations in the form and detail thereof may be made without departing from the scope of this invention. Those skilled in the art can make various changes, modifications and equivalent arrangements, which are equivalent to the embodiments of the present invention, without departing from the spirit and scope of the present invention, and which may be made by utilizing the techniques disclosed above; meanwhile, any changes, modifications and variations of the above-described embodiments, which are equivalent to those of the technical spirit of the present invention, are within the scope of the technical solution of the present invention.