KR101104627B1 - Barium titanate nano powder and method for fabricating the same - Google Patents

Abstract

The present invention, by using the mixed beads and to obtain a uniform pulverization and dispersion effects at the same time, BaCO ₃ nanosized after starting nano-milling the raw materials TiO ₂ and about the barium titanate particles and a process for producing with a nanoscale Mixing method is used, but it is dispersed by high energy mill at the first 0.65mm, 1mm mixing beads and 1600rpm at low speed, and charged into a high-energy mill for 0.1mm and 0.3mm nano grinding dispersion connected in series to grind and disperse. It relates to an invention that can be performed at the same time.

In addition, the present invention uses a mixture of rutile (58.2%) + anatase (41.8%) when using a TiO ₂ starting material, so that a smooth diffusion path can be obtained and high crystallinity of rutile phase can be used simultaneously The present invention relates to a method for obtaining high reactivity and tetragonality (c / a) compared to using other starting materials, ie, rutile or anatase single phase.

Description

BARUM TITANATE NANO POWDER AND METHOD FOR FABRICATING THE SAME

The present invention relates to a technique for forming BaTiO ₃ having a nano size by using a solid phase reaction method of low cost and easy processing.

Barium titanate (BaTiO ₃ ) is one of the most widely used ceramic materials in the industry due to its excellent dielectric properties. Currently, barium titanate (BaTiO ₃ ) accounts for 80 to 90% of the capacitor market. According to the miniaturization of electronic components, most ceramic dielectrics are manufactured in a laminated structure called a multilayer ceramic capacitor (MLCC), and this structure is tape casting, a thick film manufacturing technology developed by Howatt et al. In 1947. casting method). In general, it is known that MLCC is the most widely used electronic device with 250 cell phones, 400 notebooks, and 1000 vehicles. The MLCC has a structure in which a dielectric and an internal electrode are connected in parallel.

1A to 1C are cross-sectional views and schematic views illustrating a multilayer ceramic capacitor according to the related art.

FIG. 1A illustrates a cross-sectional view of a laminated ceramic capacitor, in which dielectric layers 10 are alternately stacked so as to be connected to both electrodes 40 alternately, and an insulating dielectric layer 20 is formed in a region therebetween. The outer surface of the dielectric layer 20 is surrounded by the case 30 and the electrode 40.

FIG. 1B realistically depicts the external appearance and internal structure of the multilayer ceramic capacitor. The dielectric film 10, the dielectric layer 20, and the case 30 and the electrode 40 may be organically coupled.

FIG. 1C is a photograph showing various types of multilayer ceramic capacitors currently used. 0603 (1.6 mm × 0.8 mm) and 0402 (1.0 mm × 0.5 mm) and 0201 (0.4) which are actually used in general home appliances. Mm x 0.2 mm).

Such MLCCs were manufactured using internal electrodes such as Pd or Pd-Ag, which are mostly expensive until 1955. However, in recent years, the Pd value fluctuates severely, making it difficult to manufacture parts.

2 is a graph showing the price trend of Pd electrodes and other precious metals.

Referring to FIG. 2, in 1990, the Pd value increased significantly. Therefore, research to use cheaper electrodes (Base-Metal Electrodes (BME)) such as Ni and Cu has accelerated.

When Ni is used as the internal electrode, the MLCC price can be reduced by 50 to 80% compared to the use of precious metals. However, when BME is used, the internal electrode is completely oxidized in an air atmosphere and thus cannot serve as an electrode. Therefore, MLCC must be sintered in a reducing atmosphere. In this case, a dielectric problem is reduced and a dual problem in which the MLCC specification cannot be satisfied. In order to solve these problems, researches related to numerous additives for securing reduction resistance have been carried out.

The capacitance of the MLCC is expressed by Equation 1 below.

[Equation 1]

Where εo is the dielectric constant in vacuum, εr is the dielectric constant of the dielectric material, N is the number of layers, A is the electrode area, and d is the dielectric thickness. In order to increase the capacitance value per unit volume, researches on increasing the dielectric constant of the dielectric material and reducing the thickness of each dielectric layer are intensively studied. Among other promising materials, barium titanate (BaTiO ₃ ), which has a higher dielectric constant than most materials, has a dielectric constant value of several thousand and a dielectric constant efficiency per volume is maximized. Therefore, most MLCCs are produced based on BaTiO ₃ raw materials, and are produced by adding small amounts of additives to control electrical, thermal and mechanical properties. Table 1 shows the characteristics of various MLCC products satisfying the EIA standard, and the amounts, dielectric constants, and temperature characteristics of BaTiO ₃ included in each product are described.

[Table 1] Characteristics of various MLCC products satisfying EIA standard

Currently, MLCC products with the maximum dielectric efficiency per volume are composed of hundreds of layers with a dielectric layer of 1 μm in thickness, and are expected to decrease further in the future to replace Ta-based capacitors or electrolytic capacitors. The most widely used MLCC size according to EIA standard is 0603 (1.6mm × 0.8mm) for general home appliances, and 0402 (1.0mm × 0.5mm) and 0201 (0.4mm × 0.2mm) size for mobile communication. It is actually used.

In general, to ensure the reliability of MLCC, it is known that at least five grains should be aligned in a direction perpendicular to the thickness of one dielectric layer. Therefore, the raw material of BaTiO ₃ can be used industrially only if it has a finer size than the thickness of the dielectric layer having strict specifications.

However, tetragonality, which is the origin of high dielectric constant (tetragonality = c / a), is known to disappear as the particle size of BaTiO ₃ (BT) decreases and disappears completely at the critical size. In addition, the MLCC manufacturing process has the complexity of implementing a high dielectric constant through a variety of different technologies including raw material processing, slip behavior control, tape casting, and sintering behavior under reduced atmosphere. However, it is basically necessary to obtain BaTiO ₃ particles having high quality nano size, high tetragonal ratio, and spherical uniform particle size distribution.

BaTiO _{3, which} has been used as a nano raw material until now, requires a spherical shape for easy dispersion, low temperature sintering characteristics with high density, high dielectric constant, low loss coefficient, and stability of a product due to lot change. Representative techniques known as a manufacturing method for this is as follows.

1) Solid State Reaction Method

2) Citrates, Oxalates

3) hydrothermal synthesis

4) solvothermal

5) alkoxide hydrolysis

6) catecholate process

7) metal-organic process

Hydrothermal and solid phase reaction methods are most widely used in the MLCC industry.

Among them, the hydrothermal method known as liquid phase reaction is close to a spherical shape, and has a narrow particle size distribution and has a form of fine particles having a small particle size difference. The hydrothermal synthesis method having this feature is a technique of heating a liquid suspension of an insoluble salt (additive) in an autoclave at high temperature and high pressure. Therefore, the crystallinity is high. In addition, the advantages of hydrothermal reactions are low energy, low pollution, simple equipment, and high precipitation reaction rate.

Usually, the particle size prepared by the hydrothermal synthesis method is suitable for thin layer production at 200 nm.

However, hydrothermal synthesis has disadvantages in spite of the above advantages. Due to the high water pressure, protons and hydroxide ions are intercalated in BaTiO ₃ crystal lattice during hydrothermal reaction, increasing the unit lattice size. Therefore, there is a disadvantage in that the density of the particles is lowered. Moreover, these defects penetrating into the lattice at the end of the MLCC sintering process are causing swelling due to emissions.

On the other hand, the above phenomenon may not occur in the case of the raw material manufactured by the solid phase reaction method. Solid phase reaction method is the most traditional BaTiO ₃ synthesis method is usually prepared by mixing the TiO ₂ powder and BaCO ₃ powder as a starting material, and then calcined at 1100 ~ 1400 ℃, milling process.

However, the raw materials produced by the conventional solid-phase reaction method has a problem of coarse particles and chemical non-uniformity and coarse particles exist as heat treated at a high temperature. Therefore, the solid phase reaction method is not suitable for the production of BaTiO ₃ powder having a nano-size.

The present invention uses a solid-phase reaction method, using a high energy mill, to achieve a uniform grinding and dispersing effect at the same time by using a mixed beads, by controlling the grinding time and temperature, excellent phase compatibility, 100nm It is an object of the present invention to provide a method for producing BaTiO ₃ having a uniform uniform average particle size and high tetragonality.

BaTiO ₃ powder manufacturing method according to the present invention is charged with BaCO ₃ in a high energy mill, and then pulverized using two kinds of mixed beads having different particle diameters and after mixing TiO ₂ to the pulverized BaCO ₃ 850 After the first calcination for 1 hour 30 minutes to 2 hours at a temperature of ~ 950 ℃ characterized in that it comprises a second calcination for 30 minutes to 1 hour at a temperature of 950 ~ 1100 ℃.

Here, the mixed beads are beads having a particle size of 0.02 ~ 0.1mm and beads having a particle size of 0.3mm, characterized in that the mixing is so as to be 1: 1 in the volume ratio of each of the beads, the high energy mill Characterized in that the rotational speed of 3000 ~ 4200rpm, the step of grinding the BaCO ₃ is carried out for 90 to 120 minutes, the step of mixing the TiO ₂ to the pulverized BaCO ₃ is the TiO ₂ And loading the pulverized BaCO ₃ into a first high energy mill including a mixed bead of 0.65 mm and 1 mm and rotating at 1500 to 1600 rpm, and then performing dispersion, and dispersing the powder on which the dispersion was performed. Further comprising the step of loading into a second high energy mill rotating at 3000 to 4200 rpm, including mixing beads having a particle diameter of 0.02 to 0.1 mm and a particle diameter of 0.3 mm while being connected in series with the energy mill, to perform pulverization dispersion. Characterized in that, the mixing beads contained in the first high energy mill and the second high energy mill are characterized in that each of the volume ratio is mixed in a ratio of 1: 1, the second high energy mill Mixing beads are characterized in that it comprises beads having a particle size of at least three, the TiO ₂ is characterized in that using a material pre-mixed with 55 to 60% by weight rutile and 40 to 45% by weight of anatase, the TiO _The molar ratio of mixing ₂ to the pulverized BaCO ₃ is characterized by mixing so that BaCO ₃ : TiO ₂ = 1.003 ~ 1.007: 1.

In addition, BaTiO ₃ powder according to the present invention is characterized in that it is prepared by the solid-phase reaction method described above is pulverized and dispersed to have a homogeneous particle size of 100nm or less.

The present invention allows to obtain a uniform grinding and dispersing effect at the same time by using a mixed beads, and provides an effect to be loaded into a high energy mill for dispersing nano-dispersion connected in series so that the grinding and dispersion can be performed simultaneously.

In addition, the present invention uses a mixture of rutile (58.2%) + anatase (41.8%) when using a TiO ₂ starting material, so that a smooth diffusion path can be obtained and high crystallinity of rutile phase can be used simultaneously Compared to the use of other starting materials, ie, rutile or anatase single phase, it provides high reactivity and tetragonality (c / a).

In the present invention, BaTiO ₃ having a nano size is formed by using a low-cost, easy-to-process solid-phase reaction method, so as to obtain a critical particle size for cubic-tetragonal phase transition, and 200nm class By systematically examining the properties of raw materials such as BaCO ₃ or TiO ₃ having the following nano-size, it is possible to manufacture BaTiO ₃ raw materials suitable for high capacity through an economical method.

Hereinafter, the barium titanate particles having a nano size and a method of manufacturing the same will be described in detail based on the technology of the present invention described above.

Advantages and features of the present invention and methods for achieving them will be apparent with reference to the embodiments described below in detail. However, the present invention is not limited to the embodiments disclosed below, but may be implemented in various forms, and only the embodiments are intended to complete the disclosure of the present invention, and are common in the art. It is provided to fully inform those skilled in the art of the scope of the invention, which is to be defined only by the scope of the claims.

Figure 3 is a schematic diagram showing a high energy mill for producing BaTiO ₃ according to the present invention.

3 shows a high energy mill using a mechanical-chemical activation process caused by high energy milling. The high energy mill has a mixing tank 100 for mixing the raw materials, and one side of the mixing tank 100 includes a circulation tube connected to the grinder cylinder 120. And, the grinder cylinder 120 is to be accurately controlled by the control device 110.

As such, the solid phase reaction method using the high energy mill according to the present invention promotes the activation of the fine starting material and the solid phase reaction to lower the reaction temperature and thus to reduce the particle size of the final synthetic material.

Figure 4 is a cross-sectional view showing the inside of the high energy mill mill cylinder for producing BaTiO ₃ according to the present invention.

High energy mill according to the present invention forms a powder having a nano size by a continuous process of the mill cylinder (120). To this end, the grinder cylinder 120 of FIG. 4 includes a rotor 200 capable of rotating at a high speed of several thousand rpm and having a disk shape, and a cooling system 230 provided to protect the outside thereof.

Insert the starting material and the final synthetic material into the inlet 210 and mix the beads 220 having a diameter of 0.02 ~ 1.0mm and then rotate the rotor 200 to pulverize and disperse into nano-sized particles, the separator (240, 250) To be discharged continuously. At this time, the general ball mill method or attrition mill is a discontinuous process and the processing time is increased to grind to the desired particle size. In the present invention, by using a high energy mill, it is possible to efficiently form a powder having a nano particle size. .

FIG. 5A is a SEM photograph showing BaCO ₃ starting material for producing BaTiO ₃ according to the present invention, and FIG. 5B is a SEM photograph showing TiO ₂ atanase for producing BaTiO ₃ according to the present invention.

Referring to Figure 5a, it shows the shape and size of BaCO ₃ raw material used as a starting material used in the present invention. Since BaCO ₃ has a needle shape unlike TiO ₂ having a spherical particle shape as shown in FIG. 5B, it is preferable to reduce the particle size by pulverizing before mixing using a high energy mill. By reducing the particle size, it was intended to increase the contact area with TiO ₂ , thereby making the diffusion path homogeneous and allowing the homogeneous grain growth to occur.

At this time, while changing the beads size (Beads size) used in the high energy mill and the rotational speed of the rotor in order to obtain the appropriate grinding conditions of BaCO ₃ as follows, the particle change and particle diameter of the powder was observed.

6a to 6f are photographs showing the particle shape and particle size change of BaCO ₃ with the grinding time when using 0.65mm beads when using the high energy mill according to the present invention.

Figure 6a is a state before grinding, Figure 6b is 40 minutes, Figure 6c is 60 minutes, Figure 6d is 80 minutes, Figure 6e is 100 minutes, Figure 6f is a 120 minutes pulverized, spherical particles having a size of 80 ~ 120nm It can be seen that at least 120 minutes must elapse before the mill can be crushed. However, here, the grinding time can be changed depending on the amount of raw materials or the capacity of the high energy mill, the present invention is not limited by the time range.

7a to 7f are photographs showing the particle shape and particle size change of BaCO ₃ according to the grinding time when using 0.2mm beads when using the high energy mill according to the present invention.

Figure 7a is a state before crushing, Figure 7b is 40 minutes, Figure 7c is 60 minutes, Figure 7d is 80 minutes, Figure 7e is 100 minutes, Figure 7f is a pulverized 120 minutes, spherical particles having a size of 50 ~ 100nm When comparing the 120 minutes to be crushed, it can be seen that the finer crushing effect can be obtained compared to the same time than in the case of FIGS. 6A to 6F.

On the other hand, the grinding efficiency may also vary depending on the number of revolutions of the high energy mill, and in order to measure the grinding efficiency for the same beads (0.2 mm), the rotor speed is changed to 3000 and 4200 rpm to determine the particle size according to the grinding time. The reduction was measured.

8A to 8C are photographs showing the change in particle shape of BaCO ₃ according to the grinding time when 0.2 mm beads are used and the rotor speed is 3000 rpm when the high energy mill according to the present invention is used.

FIG. 8A is a 30 minute pulverization at a speed of 3000 rpm, FIG. 8B is a 60 minute pulverization, and FIG. 8C is a 90 minute pulverization.

9A to 9C are photographs showing the change in particle shape of BaCO ₃ according to the grinding time when 0.2 mm beads are used and the rotor speed is 4200 rpm when the high energy mill according to the present invention is used. Is the same as the case of FIGS. 8A to 8C.

Comparing FIG. 8C and FIG. 9C, it can be seen that in the case of 3000 rpm, spherical sites of about 100 nm are formed in the same time zone, while in the case of 4200 rpm, the grinding efficiency is increased to spherical particles of about 50 nm. That is, as the rotor speed increases when the same beads are used, the energy applied to the raw materials increases and the grinding efficiency increases.

On the other hand, when BaCO ₃ and TiO ₂ are mixed wet using ultrapure water, BaCO ₃ is dissolved in water and synthesized as BaTiO ₃ . At this time, the Ba / Ti molar ratio is out of 1: 1 occurs. Therefore, when BaTiO _{3 is} synthesized, the amount of BaCO ₃ must be added to synthesize the Ba / Ti molar ratio as 1: 1 as possible.

In the present invention, in order to find the optimal Ba / Ti mole ratio for the synthesis of BaTiO _3, after mixing the mixture conditions to 3000rpm, 12 pass (pass), the Ba / Ti mole ratio was investigated using ICP wet analysis method. The results are shown in the following [Table 2]. As can be seen from the results, when mixed and pulverized with BaCO ₃ : TiO ₂ = 1.003 ~ 1.007: 1, it was found that the molar ratio of the synthesized Ba / Ti was close to 1: 1. Therefore, in the present invention, it is preferable to perform BaTiO ₃ synthesis by adding BaCO ₃ in an excess of 0.003 mol.

TABLE 2

In the above experimental results, the particle size of BaCO ₃ using the beads of 0.2 mm can be seen that the average particle diameter of the sphere is pulverized to the size of 100 nm as shown in FIG. 7F. However, it can be seen that there are also fine powders of 50 nm or less in terms of homogeneity of particle size. Such fine powders may have high reactivity, thereby causing excessive growth of particles when reacted with TiO ₂ after synthesis, thereby inhibiting uniform growth of BaTiO ₃ particles after calcination.

Therefore, in the present invention, in order to achieve uniform particle growth, the uniform grinding of BaCO ₃ should be induced. For this purpose, in the present invention, the grinding is preferably performed using mixed beads. In order to prove the critical significance for this, it will be compared with the case of using a single size 0.2mm beads and mixed beads in the following drawings.

10A and 10B are photographs showing the particle shape change of BaCO ₃ according to the type of beads and the number of passes when using the high energy mill according to the present invention.

Figure 10a shows the particle shape after passing 20pass at 3000rpm using a single 0.2mm beads, Figure 10b is a mixture of 0.3mm and 0.1mm beads in a volume ratio of 1: 1 to pass through 15apss after the particle shape Indicated.

As a result, when the mixed beads are used, the particles of BaCO ₃ are pulverized into a sphere of uniform size, while the uniformity of the particle size is reduced when the single beads are used.

Therefore, it can be seen that when the mixed beads are used, large diameter beads lead to grinding and small size beads lead to dispersion, thereby increasing the uniform dispersion effect and the uniform grinding effect. Here, based on the beads having a large particle size, it is preferable that the smaller particle size of the beads be 0.06 to 0.35 times the particle size of the large size. Therefore, based on 0.3 mm of beads having a large particle size, it is preferable to mix beads having a particle diameter of 0.02 to 0.1 mm.

On the other hand, if homogeneous particle growth occurs, the calcination temperature can be lowered, which is also related to TiO ₂ . For example, the fine particles of TiO ₂ as shown in FIG. 5B act as a catalyst to assist in the decomposition of BaCO ₃ , wherein TiO ₂ (density: 3.90 g / cm 3) on atanatase has a rutile TiO ₂ structure. Since the density is lower than (density: 4.23 g / cm 3), the calcination temperature can be lowered more efficiently. Therefore, below, it is assumed that the particle shape change of BaTiO ₃ according to the type of TiO ₂ is investigated.

Figure 11 is a photograph showing the particle shape change of BaTiO ₃ after mixing and type of TiO ₂ according to the present invention.

First, the following three kinds of TiO ₂ powder may be used to synthesize BaTiO ₃ . At this time, the BaCO ₃ powder used was the same as that of Fig. 5a pulverized using the mixing beads, the molar ratio was mixed so that BaCO ₃ : TiO ₂ = 1.003: 1 as shown in the [Table 2].

1) Rutile (Purity: 99.97)

2) Anatase (Purity: 99.74)

3) Rutile (58.2%) + Atanase (41.8%)

11 shows the results of observing the raw material shape of the starting material for each TiO ₂ with an electron microscope. After weighing using these starting materials, 1st and 0.65mm beads were firstly dispersed at 1600rpm using a high-energy mill, and then a high-energy mill containing 0.3mm and 0.1mm beads was connected and ground in series. Was carried out, and the results are shown in FIG. 11.

The starting material of TiO ₂ has a size similar to BaCO ₃ pulverized to less than 100 nm and can be mixed in a uniform distribution. In order to investigate the effect of calcination temperature on grain growth and tetragonal maintenance (c / a) for each of these mixed raw materials, calcination was carried out under the following conditions.

In this case, when the starting material is used to pulverize the nano-material, it is difficult to disperse by general stirring method, so it must be loaded directly into a high energy mill for crushing the nano-material. At this time, a situation in which the process is impossible due to the blockage of the separator due to the aggregation phenomenon may occur. Therefore, it is important to perform nano grinding after dispersing the primary dispersion at 1600 rpm using beads larger than nano grinding.

Figure 12 is a photograph showing the particle shape change of BaTiO ₃ according to the TiO ₂ type and mixing conditions according to the present invention, it shows the results of observing the particle shape of BaTiO ₃ synthesized at each synthesis temperature with an electron microscope.

Mixing conditions were carried out divided into three cases.

1) 950 ℃ 2 hours

2) 950 ℃ 2 hours + 1000 ℃ 30 minutes

3) 950 ℃ 2 hours + 1000 ℃ 1 hour

Comparing the photos shown, it can be seen that the higher the synthesis temperature, the longer the holding time (that is, when the synthesis temperature changes from 1) to 3), the particle size increases, and interparticle growth also increases. .

Generally, the lower the synthesis temperature, the lower the grain growth, but the tetragonal maintenance (c / a) decreases, resulting in a decrease in the dielectric constant. Therefore, in the present invention, it is important to be able to exhibit high tetragonal maintenance even at low temperatures. In addition, since the growth of the particles increases with time, the present invention allows to maintain for a short time at a high temperature.

13 is a graph showing the results of XRD analysis for analyzing the ratio of TiO ₂ type, phase synthesis and tetragonal phase according to the present invention.

Referring to FIG. 13, the phase synthesis and tetragonality of each synthetic powder were observed by XRD. Since tetragonal maintenance (c / a) is higher as the peaks of (002) and (200) planes are clearly separated, , The higher the synthesis temperature, the longer the retention time, the larger the particle size, and the greater the interparticle growth, the greater the neck thickness. As the thickness of the neck becomes thicker, the particle size increases, and when pulverized for MLCC synthesis, fine powder may be generated, which may be difficult to use.

On the other hand, it can be seen that tetragonality is increased in their bound form than rutile or anatase to synthesize BaTiO ₃ of high dielectric constant. Accordingly, it can be seen that the BaTiO ₃ complete solid solution phase was obtained without forming a secondary phase from the peak measured in the XRD scan range 2Θ = 20 to 80 °. In addition, the peaks scanned at 2Θ = 45 ~ 46.5 ° to show the ratio of the tetragonal phase is shown at the bottom in accordance with the respective synthesis conditions at the bottom.

Next, tetragonal maintenance (c / a) values are summarized in the following conditions obtained by the peak separation method and are shown in the following [Table 3].

[Table 3]

First, in the case of using TiO ₂ on anatase, {002} peak may be separated and maintained at 1000 ° C. for 1 hour at 950 ° C. to form a tetragonal phase with c / a = 1.0054. However, {002} peak is not separated under the conditions below, and thus it can be seen that the dielectric constant is low in the cubic phase.

However, when using TiO ₂ on rutile ({{{{}}}}} {{}}} even when maintained at 950 ° C for 2 hours, a tetragonal maintenance of c / a = 1.0052 was obtained. Therefore, it can be seen that TiO ₂ in rutile phase is more advantageous than TiO _{2 in} anatase in order to increase tetragonal maintenance at low temperature synthesis temperature.

However, when TiO ₂ on rutile is used, the tetragonal ratio is high as 1.0067 when synthesized at 950 ° C for 2 hours + 1000 ° C for 1 hour, but as shown in FIG. . In order to solve this problem, it was tested whether TiO ₂ was mixed with rutile (58.2%) + anatase (41.8%) to use a smooth diffusion path on anatase and simultaneously use high crystallinity on rutile.

As shown in FIG. 12, even when only 2 hours of 950 ° C. was maintained, the tetragonal maintenance was 1.0064. When the synthesis was performed for 2 hours + 1000 ° C. for 30 minutes using only TiO ₂ of rutile phase, high tetragonal maintenance was obtained. Could.

Next, as can be seen from FIG. 13, a 100 nm-class uniform synthetic BaTiO ₃ powder having almost no neck formation was obtained.

In addition, when 950 ℃ was synthesized for 2 hours + 1000 ℃ for 30 minutes, tetragonal maintenance had the highest value of 1.0074, and when 950 ℃ was synthesized for 2 hours + 1000 ℃ for 1 hour, tetragonal maintenance was 1.0074 at 950 ℃ for 2 hours. + 1000 ℃ 30 minutes synthesized shows similar values, but 950 ℃ 2 hours + 1000 ℃ 1 hour synthesized even though it has a high tetragonal maintenance, it can be seen that the neck (neck) growth is significantly increased compared to the other.

Therefore, the use of TiO ₂ raw material (rutile (58.2%) + anatase (41.8%) compared to other starting raw materials, due to the high reactivity can obtain a high tetragonal maintenance (c / a) at low synthesis temperature, A spherical 100 nm homogeneous BaTiO ₃ can be synthesized.

As described above, the present invention uses a solid phase reaction method for producing a ceramic powder, using a mixed bead at the same time to obtain a uniform grinding and dispersing effect of BaCO ₃ starting material, nano-dispersion is connected in series It is charged into the high energy mill to allow grinding and dispersion to be carried out simultaneously. In this case, when using a TiO ₂ starting material, by using a mixture of rutile (58.2%) + anatase (41.8%), it is possible to obtain a smooth diffusion path and to simultaneously use a high crystallinity of rutile, rutile or Compared to using anatase single phase, high reactivity and tetragonal maintenance (c / a) can be obtained.

Although the embodiments of the present invention have been described above with reference to the accompanying drawings, the present invention is not limited to the above embodiments, but may be modified in various forms, and having ordinary skill in the art to which the present invention pertains. It will be understood by those skilled in the art that the present invention may be embodied in other specific forms without changing the technical spirit or essential features of the present invention. It is therefore to be understood that the above-described embodiments are illustrative in all aspects and not restrictive.

1 is a cross-sectional view schematically showing a barium titanate powder coated with an oxide layer according to the present invention.

2 is a graph showing the price trend of Pd electrodes and other precious metals.

Figure 3 is a schematic diagram showing a high energy mill for producing BaTiO ₃ according to the present invention.

Figure 4 is a cross-sectional view showing the inside of the high energy mill mill cylinder for producing BaTiO ₃ according to the present invention.

Figure 5a is a SEM photograph showing BaCO ₃ starting material for producing BaTiO ₃ according to the present invention.

Figure 5b is a SEM photograph showing TiO ₂ atanase for the production of BaTiO ₃ according to the present invention.

6a to 6f are photographs showing the particle shape and particle size change of BaTiO ₃ with the grinding time when using 0.65mm beads when using the high energy mill according to the present invention.

7a to 7f are photographs showing the particle shape and particle size change of BaTiO ₃ with the grinding time when using 0.2mm beads when using the high energy mill according to the present invention.

8a to 8c are photographs showing the particle shape change of BaTiO _{3 with} grinding time when using a high energy mill according to the present invention using 0.2mm beads and the rotor speed is 3000rpm.

Figures 9a to 9c are photographs showing the change in particle shape of BaTiO ₃ with the grinding time when using a high energy mill according to the invention 0.2mm beads, the rotor speed is 4200rpm.

10a and 10b are photographs showing the particle shape change of BaTiO ₃ according to the type of beads and the number of passes when using a high energy mill according to the present invention.

Figure 11 is a photograph showing the particle shape change of BaTiO ₃ after mixing and TiO ₂ type according to the present invention.

12 is a photograph showing the particle shape change of BaTiO ₃ according to the TiO ₂ type and mixing conditions according to the present invention.

13 is a graph showing the results of XRD analysis for analyzing the ratio of TiO ₂ type, phase synthesis and tetragonal phase according to the present invention.

Claims (10)

Charging BaCO ₃ into a high energy mill and pulverizing the mixture using two kinds of mixed beads having different particle diameters; And Mixing TiO ₂ with the pulverized BaCO ₃ and then calcining for 1 hour 30 minutes to 2 hours at a temperature of 850 to 950 ° C., and then calcining for 2 minutes to 30 minutes to 1 hour at a temperature of 950 to 1100 ° C. BaTiO ₃ powder manufacturing method comprising a. The method of claim 1, The mixed beads are beads having a particle size of 0.02 ~ 0.1mm and beads having a particle size of 0.3mm, and the method of producing BaTiO ₃ powder, characterized in that they are mixed so as to be 1: 1 by volume ratio of each of the beads. The method of claim 2, The high energy mill is BaTiO ₃ powder manufacturing method, characterized in that having a rotational speed of 3000 ~ 4200rpm. The method of claim 1, The step of pulverizing the BaCO ₃ BaTiO ₃ powder manufacturing method, characterized in that performed for 90 to 120 minutes. The method of claim 1, Mixing the TiO ₂ to the pulverized BaCO ₃ is Charging the TiO ₂ and the pulverized BaCO ₃ to a first high energy mill including a mixed bead of 0.65 mm and 1 mm and rotating at 1500 to 1600 rpm, and then performing dispersion; And a powder having the dispersion performed in series with the first high energy mill, the mixed beads having a particle diameter of 0.02 to 0.1 mm and a particle diameter of 0.3 mm, and loaded into a second high energy mill rotating at 3000 to 4200 rpm. BaTiO ₃ powder manufacturing method characterized in that it further comprises the step of performing a grinding dispersion. The method of claim 5, Mixing beads contained in the first high energy mill and the second high energy mill are each mixed in a ratio of 1: 1 by volume ratio BaTiO ₃ powder manufacturing method. The method of claim 5, BaTiO ₃ powder method which is characterized in that the mixed beads included in the second high-energy mill comprises beads having a particle diameter of three or more types. The method of claim 1, The TiO ₂ is a method for producing BaTiO ₃ powder, characterized in that using a pre-mixed material in rutile 55 to 60% by weight and anatase 40 to 45% by weight. The method of claim 1, The molar ratio of mixing the TiO ₂ to the pulverized BaCO ₃ is BaCO ₃ : TiO ₂ = 1.003 ~ 1.007: 1 so that the mixing method for producing BaTiO ₃ powder. delete

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