KR20160026735A - An in situ Method for Producing Nanomaterials as Coating with functional materials and the Nanomaterials produced thereby - Google Patents
An in situ Method for Producing Nanomaterials as Coating with functional materials and the Nanomaterials produced thereby Download PDFInfo
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Abstract
Description
The present invention relates to a method of coating a surface with a functional material while simultaneously manufacturing a nanomaterial in situ. More specifically, the present invention relates to a method of manufacturing a nanomaterial in situ using a thermal plasma, Coating a surface of a nanomaterial with a metal or the like to produce a desired functional nanomaterial, and a functional organic-coated nanomaterial produced thereby.
Nanomaterials, which account for a significant portion of high-tech materials, exceeded $ 1.7 billion in 2010 with a market growth rate of 10.4% per annum for five years ($ 16 billion for the global nanotechnology market). Among them, North America has a market share of 38%, a growth rate of about 25%, a market of 37% in Europe and a growth rate of about 22% in Europe and a growth rate of about 32% in Asia. The Asian market is expected to grow rapidly and become the largest part of the global market. The nanomaterial market is expected to grow at an average annual rate of 23% to $ 5.8 billion by 2016 and is expected to lead the health and energy storage industry
The physical properties of the material are not completely fixed according to the composition (composition) but have a size dependency that varies depending on the size of the structure constituting the material. Nanomaterials are materials that depend on the size dependence of physical properties in the nanometer size range (1 to 100 nanometers) much smaller than the micron or submicron (below micron) size structures of existing materials. Unusual is that the physical properties of the material continuously change in proportion to the size of the structure (or in inverse proportion) until the structure of the material becomes submicron. However, if the size of the material is reduced to the nanometer size region, Lt; / RTI > Nanomaterials are materials that utilize discontinuous or newly emerging physical properties in the nanometer range.
Recently, interest in nanotechnology has been increasing due to the rapid development of electronics, information communication, and biotechnology. As the particle size of nano powder has become very small, new unique properties that were not observed in general powders are observed. Of course, the expectation for application of nano powder over various industrial fields such as high-strength mechanical parts, catalysts, pharmaceuticals and biotechnology is getting higher.
Particularly, with the miniaturization and high functionality of electronic devices, metal nanoparticles have attracted attention as materials used for wiring and electrode formation. When the particle size of the metal particles is about 100 nm, the sintering temperature is lowered to 200 DEG C or less, and the metal particles can be bonded even at a relatively low temperature, so that the metal particles can be used as a wiring material having low resistance regardless of the substrate material. Such metal nanoparticles are particularly important because they can be applied to flexible substrates.
There are various methods for making metal nanoparticles, such as a spray-making method, a sol-gel method, and an electric explosion method. Metal nanoparticles are difficult to produce and difficult to obtain high-quality powder due to deterioration of properties due to an oxide film formed at the time of manufacturing . For example, when manufacturing metal nanoparticles, the particles are collected using a cold trap, a sieve, or a cyclone after the raw material is evaporated or made into nano-sized fine particles by using plasma. In this case, There has been a problem in that coagulation occurs in the collection process even when not in contact with the outside, and the surface is oxidized by being in contact with air while being transported for other uses.
Accordingly, the present inventors have made efforts to find a method for preventing agglomeration, improving dispersion and surface oxidation in the production of nanomaterial including metal, metal oxide, ceramic carbon nanocomposite, etc., It is possible to coat functional materials simultaneously with nanomaterial production by coating organic materials or transition metals in situ. Thus, the present invention has been completed.
It is an object of the present invention to provide a method for coating a surface with a functional material while simultaneously preparing a nanomaterial in situ, that is, a method for in situ production of an organic material or a transition metal coated nanomaterial.
Another object of the present invention is to provide various uses of organic materials or transition metal coated nanomaterials produced by the above method.
In order to solve the above problems,
In one embodiment, the present invention provides a method for in situ preparation of an organic or transition metal coated nanomaterial, comprising:
(a) vaporizing the nanomaterial by thermal plasma,
(b) quenching by gas injection,
(c) introducing a coating material of an organic material or a transition metal to vaporize or activate the coating material,
(d) forming an organic or transition metal coating layer on the surface of the nanomaterial, and
(e) obtaining an organic or transition metal coated nanomaterial.
In particular, the method is characterized by coating the surface with a functional material while simultaneously producing the nanomaterial in situ.
At this time, in step (a)
The nanomaterial may be a metal or a metal oxide present as a solid at room temperature; Magnetic nanomaterials; And a carbon-based material, and argon gas is preferably used as a gas for use in generating the thermal plasma.
For example, the metal or metal oxide may be selected from the group consisting of B, C, Mg, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Sr, Y, Zr, In, Sn, Sb, Ta, W, and combinations thereof, and the magnetic nanomaterial may be Sr-ferrite or Br-ferrite. In one embodiment of the present invention, Ni, Cu, Sn, a carbon-based material and SrFe 12 O 19 were used.
The nanomaterial is characterized in that the nanomaterial undergoes nuclear growth while passing through the plasma according to the step (a).
Further, in the step (b)
Quenching can be accomplished by injection of quenching gas, preferably argon gas. Particularly, by this quenching, the size of the nanomaterial can be controlled in the range of 10 to 150 nm.
The organic material may be selected from the group consisting of benzene, aniline, dopamine, phenol, benzylamine, phenethylamine, pyrocatechol, 2-hydroxypyridine hydroxypyridine, hydroxypyridine, hydroxypyridine, anthracene, naphthalene, 2-naphthol, 9-anthracenol, 2-anthraquinone, Anthracenol, and 1-anthracenol. Preferably, benzene, aniline, or dopamine is used. In one embodiment of the present invention, aniline was used.
Particularly, in step (d), the thickness of the organic material or the transition metal coating layer is 10 to 50 nm, preferably 20 to 40 nm.
As a preferred embodiment of the present invention, the organic material coated nanomaterial prepared by the above method is 1 to 40 nm in thickness, and the nanomaterial is selected from the group consisting of Ni, Cu, Sn, graphene and SrFe 12 O 19 , and the organic material may be carbon, aniline, or dopamine. In one embodiment of the present invention, the aniline precursor of the organic material on the surface of the nanomaterial is polymerized to form (poly) dopamine.
As described above, the present invention relates to a method of manufacturing a nanomaterial by in-situ production of a nanomaterial using a thermal plasma and coating the surface of the nanomaterial with an organic material or a transition metal that imparts functionality to produce a desired functional nanomaterial, It is possible to provide a nanomaterial which is functionalized on its surface to improve its properties, prevent aggregation, improve dispersibility and solve the problem of surface oxidation, and can be usefully used for various purposes.
FIG. 1 is a conceptual diagram of a thermal plasma apparatus that can be used for the in situ manufacturing method of the nanomaterial of the present invention.
FIG. 2 is a schematic diagram of a temperature profile in which the introduction portion of the coating material can be determined in the in situ manufacturing method of the nanomaterial of the present invention. FIG.
3 is yes the pin / nickel (Ni) nanomaterials CH 4 SEM and TEM images of nanocomposites prepared by in situ coating.
4 is yes the pin / copper (Cu) nanomaterials CH 4 SEM and TEM images of nanocomposites prepared by in situ coating.
5 is an SEM and TEM image of a nanocomposite prepared by aniline in situ coating of a graphene / nickel (Ni) (10: 1) nanomaterial.
6 is an SEM and TEM image of a nanocomposite prepared by aniline in situ coating of a graphene / copper (Cu) (10: 1) nanomaterial.
7 is an SEM and TEM image of a nanocomposite prepared by aniline in situ coating of a graphene / tin (Sn) (10: 1) nanomaterial.
8 is an SEM and TEM image of a nanomaterial prepared by aniline in-situ coating of a nickel (Ni) nanomaterial.
9 is a schematic diagram of a simulation temperature profile for setting in-situ coating process conditions using an aniline (C 6 H 5 NH 2 ) precursor.
10 is a schematic diagram of a calculation method for deriving an input amount of aniline (C 6 H 5 NH 2 ) and a metal input amount.
11 is a value measured using an infrared spectrophotometer.
12 to 14 are copper (Cu) and nickel (Ni) based on the organic material for the nano-material is by, AgNO 3 precipitation reaction to determine whether the coating (Ag) is the result, and FE-SEM images confirming the precipitation.
15 is an FE-SEM photograph of a nano material produced by coating an SrFe 12 O 19 nanomaterial with aniline.
16 is a schematic configuration diagram of a plasma processing apparatus according to the present invention.
Hereinafter, the present invention will be described in detail.
The present invention relates to a method of coating a surface of a nanomaterial with a functional material while simultaneously forming a nanomaterial in situ using a plasma process, preferably a thermal plasma process. In another aspect, the present invention relates to a method of coating a functional material (organic material, Or a method of producing the nanomaterial.
In the present invention, the term "nanomaterial" or "nanocomposite" refers to a material or a composite material that utilizes the dependency of physical properties on a nanometer scale region (1 to 100 nanometers). In the present invention, a variety of metals, ceramics, Fields. And preferably includes nano materials such as metals, metal oxides, and ceramics. Such nanomaterials can be applied in various forms such as powder, tube, whisker, thin film, and bulk.
"Coating" or "surface treatment" refers to a process in which a functional material such as an organic material or a transition metal, which is a coating material, is laminated on a surface of a nanomaterial or a process in which a nanomaterial surface is recombined with a gaseous environment and a plasma discharge.
Ten plasma
A method of synthesizing and co-evaporating a material having various chemical components and a crystal structure in a vaporized state and at the same time can be classified into a chemical vapor deposition (Vapor Deposition) and a physical vapor deposition (Vapor Deposition). Plasma spray coating is one of techniques for thin film coating in such a gaseous state.
The method of the present invention is characterized by using a thermal plasma process.
Thermal plasma is a gas composed of electrons, ions, and neutral particles generated mainly by arc discharge, and the particles are in the form of high-speed jet flame having 1,000 to 20,000 ° C and 100 to 2,000 m / s. By using the characteristics of thermal plasma having such high temperature, high heat capacity, high speed and large amount of active particles, it can be used as various high-efficiency heat sources and physicochemical reactors which can not be produced by conventional technology, have
As a typical method of generating a thermal plasma, a plasma apparatus generating a DC or AC arc discharge and a high frequency plasma generated by a radio frequency magnetic field are mainly used.
A plasma torch type in which a plasma is jetted from an electrode on a nozzle as a high-speed high-temperature jet is variously designed and put into practical use by a method of plasma-forming a gas by DC or AC arc discharge using an arc discharge.
More preferably, a high-frequency plasma is used in the present invention. The high-frequency induction discharge is electromotive, and usually there is a discharge in the quartz tube with the coil on the outside. When a high-frequency current is supplied, an induced current flows in the discharging part together with an induction magnetic field which changes in the same period, so that a resistance heat is generated and the thermal plasma state is normally maintained. This high-frequency thermal plasma is called inductively coupled plasma. Since the prototype of the quartz tube torch that generates high frequency induction plasma was released in the early 1960's, there was no fundamental change in its structure, A torch has been developed and marketed.
The method of the present invention can be carried out using such a known high-frequency plasma apparatus. A thermal plasma apparatus serves as a heat source for causing a physical phase change by melting and vaporizing an object material at a high temperature and a high temperature, or as a chemical reaction furnace for promoting a chemical reaction by radicals such as generated ions, excited atoms and molecules Have many
Currently, the interest in thermal plasma technology is divided into two parts: material process and waste treatment. The material process technology related to the present invention includes high-functional surface modification using new plasma, new material creation, new material production and processing These include plasma spray coating, plasma synthesis, thermal plasma chemical vapor deposition (TPCVD), metal metallurgy, material densification, physical property analysis, cutting welding and surface strengthening.
Particularly, the present invention provides a technique for creating a new material using a thermal plasma and a new material in which the surface of the created nano-new material is coated with a different material (organic material, transition metal).
In one aspect, the present invention provides a method for producing a nanomaterial coated with a functional material, which comprises the steps of producing a nanomaterial (nanocomposite) using a thermal plasma process and coating a desired functional material.
The method of the invention is carried out in-situ.
The in-situ method of the present invention is a method of manufacturing a nanomaterial (nanocomposite) by using a thermal plasma, for example, a method of manufacturing a nanomaterial composed of a metal or a metal oxide, Is a method for producing a functional nanomaterial for functionalization of a surface of a nanomaterial to enhance its properties, to prevent aggregation, to improve dispersibility, and to solve surface oxidation by adding an organic or transition metal material as a coating material.
The in-situ method has the following advantages in comparison with the method of separately coating an organic material after manufacturing the nanomaterial.
(i) Nano material synthesis and nanomaterial coating are simultaneously carried out in-situ in a thermal plasma apparatus, which lowers the process cost, shortens the process time, and simplifies the process steps. Conventional separate coating processes are disadvantageous in that the process cost is high, the process time is long, and the process steps are very complicated because nanomaterial synthesis equipment and nanomaterial coating equipment must be separately installed.
(ii) is faster, eco-friendly and economical than when coated separately.
(iii) Since an organic material or a transition metal coating is formed simultaneously with the synthesis of a nanomaterial in a thermal plasma apparatus, an oxidation preventive film is formed without exposure to the atmosphere, and a specific function of the nanomaterial synthesized by forming a coating film of organic materials and transition metals is given .
(iv) In addition, co-coated surfaces are very uniform and defect free since synthesis and coating of nanomaterials takes place in a short period of time.
The present invention, as one embodiment, can provide a method for in situ production of an organic or transition metal coated nanomaterial, comprising the steps of:
(a) vaporizing the nanomaterial by thermal plasma,
(b) quenching by gas injection,
(c) introducing an organic substance or a transition metal coating material to vaporize or activate it,
(d) forming an organic or transition metal coating layer on the surface of the nanomaterial, and
(e) obtaining an organic or transition metal coated nanomaterial.
In particular, the method is characterized by coating the surface with a functional material while simultaneously producing the nanomaterial in situ.
Hereinafter, the above method will be described as an example of a more specific process. At this time, a configuration using the plasma apparatus of Fig. 16 may be exemplified by the following description:
(1) a step of generating a thermal plasma,
② Nanomaterial Raw material (nanomaterial) injection stage,
(3) Nano material raw material (nanomaterial) is vaporized by thermal plasma,
(4) a step of performing nuclear growth after passing through a plasma,
(5) A quenching step (mass gas injection) for controlling to a certain size,
⑥ step that is fixed to a certain size of nanomaterial,
(7) charging the desired coating material in a temperature range that is capable of vaporizing or activating,
(8) the desired coating material is vaporized or activated,
⑨ the step of coating the surface of the nanomaterial, and
(10) recovering the coated nanomaterial,
First, a thermal plasma is generated (1)
When a thermal plasma is generated, the gas to be used can be classified into a sheath gas, a central gas, a carrier gas, or the like depending on its function. These gases include an inert gas such as argon, hydrogen, nitrogen Or a mixture thereof may be used. Argon gas is preferably used.
The sheath gas is injected to prevent vaporized particles from adhering to the inner surface of the wall and also to protect the wall surface from ultrahigh plasma, and can use 30 to 150 lpm (liters per minute) of argon gas, Is a gas which is injected to generate a high temperature thermal plasma and can use argon gas of 30 to 120 lpm. The carrier gas serves to supply mixed powder to the inside of the plasma reactor, and argon gas of 3 to 20 lpm Can be used.
16, the
The nanomaterial, the raw material of the nanomaterial, is injected into the thermal plasma generator (2)
The nanomaterial is a material in the range of 1 to 100000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 (one meter) And carbon-based and ceramic-based materials, and more preferably one selected from among an alkali metal, an alkaline earth metal, a lanthanum, an actinium, a transition metal, a transition metal, and a quasi-metal on the periodic table of the elements Can be used. Most preferably, at least one of B, C, Mg, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Sr, Y, Zr, Nb, Mo, , Ta, W, or a combination thereof.
Such nanomaterials can be provided by using a quantitative feedstock supply apparatus as much as the amount of the feedstock to be used. In Fig. 16, the
As a preferred embodiment, the following nanomaterials can be used.
Si is an anode material of lithium secondary battery. It minimizes the capacity decrease by surface oxidation in the production of nano Si, so that the theoretical capacity of 4,200 mA / can be maximized. By dispersing individual particles of nano material through surface coating, In manufacturing a negative electrode material for a lithium secondary battery, it is possible to minimize the damage of the battery due to expansion during charging and discharging caused by accumulation of nanosilicon in one place. In addition, electrical conductivity and dispersibility can be improved by inhibiting surface oxidation of nano Cu, Sn, and Ag, which are conductive ink materials for electric and electronic electrodes. At this time, it is preferable to coat with the same components as the dispersion solvent used in the conductive ink.
In addition, a material for a magnetic nanomaterial may be used for manufacturing the nanomaterial of the present invention.
The magnetic polymer particles in which iron oxide nanoparticles are dispersed therein include, for example, ferrite nanomaterials such as Sr-ferrite and Br-ferrite (SrFe 12 O 19 , BaFexOx, etc.).
The magnetic polymer particles can be prepared by various methods. The simplest method is to encapsulate iron oxide nanoparticles having a superparamagnetic property with a polymer. When the monomers are emulsion-polymerized in the presence of stabilized iron oxide nanoparticles such as ferrofluid, magnetic polymer particles encapsulated with iron oxide nanoparticles can be obtained. Hydrothermal, glicinenitrate, citric acid, sol-gel method and the like can be used for the production of nano-sized ferrite, which can be referred to a known technique [M. Serkol, Y. Koseoglu, A. Batkal, H. Kavas, and A. C. Bazaran, J. Magn. Magn. Mater. 321, 157 (2009); S. Hajarpour, A. H. Raouf, and Kh. Gheisari, J. Magn. Magn. Mater. 363, 21 (2014); A. Thakur, R. R. Singh, and P. R. Barman, J. Magn. Magn. Mater. 326, 35 (2013); H. Anwar and A. Masqsood, J. Magn. Magn. Mater. 333, 46 (2013).
The nanomagnetic material (Sr-ferrite, Br-ferrite) can be improved in dispersibility and orientation properties by coating with an organic material such as aniline or dopamine. In the process of making magnet, the coercivity at the grain boundary due to nucleation is easily generated in the bonding surface of the magnetic material during the firing process, and the coercive force is lowered to about 20% of the theoretical value. It is because. In order to improve the saturation magnetization of the magnetic material, it is also possible to use a ferrite of a different kind having a large saturation magnetization value or a core-shell structure of a multi-species metal hexaferrite nanoparticle coated with a metal such as Co, Ni, Metal hexafelite nanoparticles may be prepared to improve the magnetic properties.
Further, the nanomaterial of the present invention can use a carbon-based material (for example, graphene, graphite or the like). Also, a nano-metal-graphene fusion structure having a structure in which the nanomaterial is crystallized in the carbon-based material may also be used. For details of such nano-metal-graphene fusions, refer to Korean Patent No. 10-1330227.
Next, the injected nanomaterial is vaporized by using a thermal plasma (3).
The thermal plasma is an ionizing gas composed of electrons, ions, atoms and molecules generated from a plasma torch using DC arc or high frequency inductively coupled discharge, and is a high-speed jet having an extremely high temperature ranging from thousands to tens of thousands K and a high activity .
Therefore, in order to smoothly generate a high-temperature plasma, an arc is formed by electric energy and a power of 10 to 70 kW is supplied to the power supply of the plasma apparatus, and argon gas, which is used as a thermal plasma generating gas, An ultra-high temperature plasma is generated.
As described above, the ultrahigh-temperature thermal plasma generated by using argon gas as a gas while maintaining a power of 10 to 70 kW is generated at a higher temperature than the thermal plasma generated by the heat treatment method or the combustion method
The material vaporized by the ultra-high-temperature thermal plasma forms a nucleus in the specific nucleus formation temperature range of each material as it passes through the plasma region, and the nucleus formed is seeded and crystallized into a nanomaterial.
Coating materials such as organic materials and transition metals injected into the high-temperature region of the plasma are vaporized instantaneously, adsorbed on the surface of the nanomaterial moving with flow, and the coating is formed. At this time, the core- .
Then, by controlling the cooling rate, the size of the nanomaterial is controlled (⑤ and ⑥).
When a nanomaterial of a desired size is formed, it is condensed or quenched by a quenching gas to inhibit the growth of the nanomaterial, and the nanomaterial is fixed to a certain size within a range of 10 to 150 nm.
That is, the nanomaterial grown to a predetermined size is conveyed by the
Then, a coating material for functionalizing the surface of the nanomaterial is charged and activated or vaporized (⑦ and ⑧)
The coating material that can be used at this time obviously can be appropriately selected by a person skilled in the art according to the desired function and is preferably selected from the group consisting of transition metals (Co, Ni, Mn, Ti and the like), organic materials (ammonia, dopamine, Etc.) can be used. At this time, the selected coating material is introduced at a temperature range that is capable of being vaporized or activated. That is, the temperature profile of the entire thermal plasma system can be checked to determine the beginning of the coating material (Figure 2)
Preferred examples include benzene, aniline, dopamine, phenol, benzylamine, phenethylamine, pyrocatechol, 2-hydroxypyridine ( hydroxypyridine, 3-hydroxypyridine, 4-hydroxypyridine, anthracene, naphthalene, naphthol, 9-anthracenol, 2- anthracenol, and 1-anthracenol may be used.
The "aniline" used in one embodiment of the present invention is C 6 H 5 NH 2 and has a merit of being easily supplied in a gaseous state while maintaining a liquid state at room temperature having a melting point of -6.3 ° C.
[aniline]
Aniline can be obtained commercially by hydrogenating nitrobenzene under a catalyst or by reacting chlorobenzene with ammonia, or by reducing nitrobenzene with an iron catalyst in an aqueous acid solution. Aniline, the primary aromatic amine, is a weak base and reacts with inorganic acids to form salts. In one embodiment of the present invention, the aniline precursor was used as a starting material.
In addition, dopamine can be used as a coating material.
[Dopamine]
The dopamine is a monomolecular material with a molecular weight of 153 (Da) with catechol and amine functional groups (C 8 H 11 NO 2 ).
In addition, other catecholamine precursor materials described above can be appropriately selected and used. For example, pyrocatechol with a hydroxyl group (-OH) attached to the benzene ring, benzylamine with one benzene ring, two methylene bridges and one amine group attached to the benzene ring, , Phenethylamine, 2,3-dihydroxynaphthalene which is a structure attached to naphthalene in which two hydroxyl functional groups are sublimable, 1-naphthylmethylamine having an amine functional group in naphthalene ( naphthylmethylamine) may also be used. In addition, it is possible to synthesize a coating film by inducing a hydroxylation reaction or an amination reaction by controlling plasma chemistry on benzene, cyclohexane and a base unit.
In addition, specific functionalities can be imparted by coating low melting point metal (Sn, Ag, Al, etc.) among the transition metals.
By vaporization or activation of such a coating material, a coating layer can be formed on the surface of the nanomaterial described above. That is, the nanomaterial of the present invention is prepared by coating an organic material (a metal having a low melting point as necessary) on the nanomaterial.
In particular, the method of the present invention is characterized by coating the surface with a functional material while simultaneously manufacturing the nanomaterial in situ.
At this time, as one preferred embodiment of the present invention, a high frequency RF (Radio Frequency) RF power of 2 MHz, a pressure of 100 to 500 Torr under a power of 20 kW to 60 kW, The reaction is carried out.
It is obvious that the thickness of the organic coating layer can be appropriately adjusted by a person skilled in the art depending on the kind of the nanomaterial, but it is coated to about 1 to 50 nm or about 1 to 40 nm, or about 1 to 30 nm. In one embodiment of the present invention, the surface of the nanomaterial is coated with about 1 to 30 nm.
The desired organic or transition metal functional material is coated on the surface of the nanomaterial by the process described above (9), and finally the functional material-coated nanomaterial is recovered (10)
6, the nanomaterial generated in the stainless
The obtained nanomaterial coated with the functional material can be 10 to 500 nm, 20 to 500 nm, 30 to 500 nm, 40 to 500 nm, or 50 to 500 nm, although the size of the nanomaterial can be adjusted according to the purpose.
In another aspect, the present invention includes various uses of nanomaterials coated with an organic material or transition metal functional material obtained by the above-described method of the present invention.
From golf clubs to consumer electronics displays, there are many different markets for nanomaterials. Currently, the market for electronic products, automobiles, and home / building cleaners is becoming more prominent, and the market for groceries and personal care products is expected to grow. Due to the growing demand for new functions in consumer and daily necessities, the nanomaterial market for general consumer goods is expected to grow from US $ 1.7 billion in 2010 to US $ 5.3 billion by 2015
And can be used in a variety of electronic and microelectronic applications. Electronic components that may be manufactured by other printing methods such as, for example, printable displays, RFID, photovoltaic cells, computer memory, and the like; Heat dissipation materials for extending the life of electronic devices such as displays, LEDs and other lighting devices and computer parts; It is expected to be used in various fields including electrochemical devices such as next generation electronic devices, solar cells, and fuel cells. The "electrochemical device" includes an energy storage device, an energy conversion device, a sensor, and other devices that convert electrical energy into chemical energy or convert chemical energy into electrical energy. The term "energy storage device" as used herein includes batteries and super capacitors.
Ultra-high-capacity capacitors and organic solar cells incorporating polymer materials have excellent value for use as clean energy storage and conversion media due to flexibility and ease of structural control inherent in polymer materials. Organic light emitting devices can be bent, folded, or stretched in the future , It is expected to be widely applied to new types of display and lighting industries as well as clothing and buildings
As described above, the nanomaterial coated with an organic material or transition metal functional material having excellent characteristics can be used in various fields.
Example
Hereinafter, the present invention will be described in more detail with reference to Examples. It is to be understood by those skilled in the art that these examples are for illustrative purposes only and that the scope of the present invention is not construed as being limited by these examples.
Example One: CH 4 In - situ Depending on coating Grapina Nanocomposite
1-1. Produce
Carbon-based material graphene; (CH 4 ) gas as a coating material and nickel (Ni) and copper (Cu) as raw material powders, and a high-frequency thermal plasma apparatus for processing the manufacturing process according to the present invention, 30 lpm and 50 lpm of argon gas were injected, and experiments were carried out with no equilibrium gas.
At this time, the manufacturing process conditions were designed as follows:
- RF
- Plasma gas (Ar
-
1-2. SEM And TEM Image measurement
FIGS. 3 and 4 show SEM and TEM image measurement results of the nanocomposite prepared in Example 1-1, respectively.
As a result of SEM and TEM image measurement, it was found that carbon and nickel were well coated on the surface of nickel and tin, and the thickness of coating layer was 1 ~ 5 nm.
Example 2: Aniline In - situ Depending on coating Grapina Manufacture of nanocomposites
2-1. Produce
Carbon-based materials graphene; And an aniline as an organic material coating material, and a manufacturing process according to the present invention is prepared. The high-frequency thermal plasma apparatus includes a central gas and a sheath gas, Argon gas of 30 lpm and 50 lpm, respectively, was injected and the experiment was carried out without injecting equimolar gas.
At this time, the manufacturing process conditions were designed as follows:
- RF
- Plasma gas (Ar
-
2-2. SEM And TEM Image measurement
5 to 7 show SEM and TEM image measurement results of the nanocomposite according to Example 2-1, respectively.
SEM and TEM images showed that aniline (organic material) was well coated on the surface of nickel and tin, and the thickness of the coating layer was about 1 ~ 5 nm.
Example 3: Manufacture of aniline-coated nanomaterials
3-1. Produce
Nickel (Ni), copper (Cu), and tin (Sn) were used as a raw material powder and aniline as an organic material coating material as nano materials.
The temperature distribution in the reactor was simulated and experimentally verified to use the high-frequency thermal plasma method to process the manufacturing process according to the present invention (FIG. 8). Simulation results show that the reactor bottom temperature is above 500 ℃ during the 30 kW fuselage process and 100% vaporization condition is used to confirm the injection position of the liquid aniline precursor.
Then, 0.25 to 0.31 g of aniline precursor per g of metal was added at a weight ratio. The specific input weight ratios for each metal are shown in Fig.
30 and 50 lpm of argon gas were injected as the central gas and the sheath gas, respectively.
At this time, the manufacturing process conditions were designed as follows:
- RF
- Plasma gas (Ar
-
3-2. SEM And TEM Image measurement
FIG. 10 shows SEM and TEM image measurement results of the aniline-coated nickel (Ni) nanomaterial prepared in Example 3-1, respectively.
SEM and TEM images showed that aniline was well coated on the nickel surface.
3-3. FT - IR
The values measured using an infrared spectrophotometer are shown in Fig.
Example 4 : AgNO 3 Precipitation reaction
The precipitation of Ag was confirmed by the AgNO 3 precipitation reaction in order to confirm the polymerization (polypodamine formation) of the aniline precursor on the surface in the nanocomposites and nanomaterials produced by the aniline in-situ coating method.
The results are shown in Figs. 12 to 14. Fig.
That is, by using the oxidation / reduction power of the organic material (polypodamine), AgNO 3 Through the reduction reaction, it was confirmed that Ag was precipitated, so that coating of organic material (polypodamine) was well formed.
Example 5: Aniline-coated SrFe 12 O 19 Nanomaterial
5-1. Produce
In a manner similar to that of Example 2-1, aniline-coated SrFe 12 O 19 Nano materials were prepared.
At this time, the manufacturing process conditions were designed as follows:
- RF
- Plasma gas (Ar
- Ching gas (Ar 150 lpm)
- The process pressure is 500 Torr
5-2. FE - SEM Image measurement
FIG. 15 is a graph showing the transmittance of aniline-coated SrFe 12 O 19 The FE-SEM image measurement results of the nanomaterial are shown.
As a result of the FE-SEM image measurement, it was found that aniline was well coated on the surface of the magnetic material SrFe 12 O 19 , and it was confirmed that the thickness of the coating layer was 30.6 nm.
While the present invention has been described with reference to exemplary embodiments and drawings, it is to be understood that the invention is not limited to the disclosed exemplary embodiments, but, on the contrary, And variations are possible. Accordingly, it is intended that the scope of the invention be defined by the claims appended hereto, and that all equivalent or equivalent variations thereof fall within the scope of the present invention.
"About" means that the reference quantity, level, value, number, frequency, percentage, dimension, size, quantity, weight or length is 30, 25, 20, 25, 10, 9, 8, 7, , Level, value, number, frequency, percent, dimension, size, quantity, weight, or length that varies from one to three, two, or one percent.
Throughout this specification, the words " comprising "and" comprising ", unless the context requires otherwise, include the stated step or element, or group of steps or elements, but not to any other step or element, And that they are not excluded.
1: gas feeder 3: feeder
4a: Carrier
4c: Sheath gas supply line 4d: Equation gas supply line
5: plasma power supply unit 6: plasma generating electrode unit
7: Plasma reaction part and cooling part
30: Cyclone part 31: Transfer piping
50: Collector 55: Filter
60: Vacuum pump 70: Vacuum pump
71: heat exchanger
Claims (14)
(a) vaporizing the nanomaterial by thermal plasma,
(b) quenching by gas injection,
(c) introducing a coating material of an organic material or a transition metal to vaporize or activate the coating material,
(d) forming an organic or transition metal coating layer on the surface of the nanomaterial, and
(e) obtaining an organic or transition metal coated nanomaterial.
The nanomaterial may be a metal or a metal oxide present as a solid at room temperature; Magnetic nanomaterials; And a carbon-based material.
Wherein the gas used in generating the thermal plasma is argon gas.
Characterized in that quenching is carried out by injection of argon gas, which is a quenching gas.
Wherein the size of the nanomaterial is controlled in the range of 10 to 150 nm by the quenching.
Wherein the thickness of the organic or transition metal coating layer is 1 to 50 nm.
The thickness of the organic or transition metal coating layer is 1 to 40 nm,
Wherein the nanomaterial is at least one material selected from the group consisting of Ni, Cu, Sn, graphene and SrFe 12 O 19 , and the organic material is carbon, aniline or dopamine Nanomaterials.
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| KR20190099837A (en) | 2018-02-20 | 2019-08-28 | 강원대학교산학협력단 | Carbon-nano metal composite with 3D structure and it preparation method |
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| KR20190099837A (en) | 2018-02-20 | 2019-08-28 | 강원대학교산학협력단 | Carbon-nano metal composite with 3D structure and it preparation method |
| KR20190100084A (en) | 2019-08-02 | 2019-08-28 | 강원대학교산학협력단 | Carbon-nano metal composite with 3D structure and it preparation method |
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