KR20040072991A - Method for manufacturing Nano Fe-base powder with mill scale - Google Patents
Method for manufacturing Nano Fe-base powder with mill scale Download PDFInfo
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- KR20040072991A KR20040072991A KR1020030008688A KR20030008688A KR20040072991A KR 20040072991 A KR20040072991 A KR 20040072991A KR 1020030008688 A KR1020030008688 A KR 1020030008688A KR 20030008688 A KR20030008688 A KR 20030008688A KR 20040072991 A KR20040072991 A KR 20040072991A
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/16—Making metallic powder or suspensions thereof using chemical processes
- B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
- B22F9/20—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/05—Metallic powder characterised by the size or surface area of the particles
- B22F1/054—Nanosized particles
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B22F9/00—Making metallic powder or suspensions thereof
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- B22F9/04—Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
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- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/04—Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
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Abstract
Description
본 발명은 철강제조공정에서 얻어지는 부산물인 밀스케일을 이용해 Fe계 나노분말을 제조하는 방법에 관한 것으로, 보다 상세하게는 밀스케일 및 다른 종류의 금속산화물을 이용해 Fe계 나노분말을 제조하는 방법에 관한 것이다.The present invention relates to a method for producing a Fe-based nanopowder using a mill scale as a by-product obtained in the steel manufacturing process, and more particularly to a method for producing a Fe-based nanopowder using a mill scale and other metal oxides. will be.
이하의 명세서에서, 용어 "Fe계 나노분말"은 복합상의 Fe계 나노분말 및 합금상의 Fe계 나노분말을 모두 포함하는 의미이다.In the following description, the term "Fe-based nanopowder" is meant to include both Fe-based nano-powder of the composite phase and Fe-based nanopowder of the alloy phase.
종래에, 두 종류의 금속산화물을 고에너지 볼밀에 의해 분쇄혼합한 후 수소환원하여 나노분말을 제조하는 방법이 특허 제 97-1558호에 개시되어 있다.Conventionally, Patent No. 97-1558 discloses a method for preparing nanopowders by grinding and mixing two kinds of metal oxides by high energy ball mill and then hydrogen reduction.
상기 종래의 방법은, 취약한 금속산화물을 원료분말로 사용하므로, 짧은 볼밀만으로 미세한 산화물 입자를 제조할 수 있어 볼밀시의 불순물 오염을 최소화할 수 있고, 또한 극대화된 표면적 효과를 이용하여 낮은 온도로 수소환원하는 과정에서 두 금속간의 자발적 합금화를 유도화하므로 기존의 합금분말 제조공정에 비해 훨씬 유리하다는 효과를 갖고 있다.Since the conventional method uses a weak metal oxide as a raw material powder, fine oxide particles can be produced with only a short ball mill, thereby minimizing impurity contamination in the ball mill, and using a maximized surface area effect to reduce the water temperature. In the reduction process, spontaneous alloying between two metals is induced, which has the advantage that it is much more advantageous than the conventional alloy powder manufacturing process.
또한, 상기 종래의 방법은 산화물의 수소환원시 발생되는 부산물로 수증기 외에는 없으므로 환경적인 측면에서도 매우 유리하다.In addition, the conventional method is very advantageous from an environmental point of view because there is nothing other than water vapor as a by-product generated during hydrogen reduction of an oxide.
하지만, 종래의 방법은 고순도의 시약분말을 원료산화물로 사용하므로 제조비용이 크며 원료산화물의 안정적인 수급이 어렵다는 문제점을 가지고 있었다.However, the conventional method has a problem in that the production cost is high and the stable supply and demand of the raw material oxide is difficult because high-purity reagent powder is used as the raw material oxide.
이에 따라, 고가의 원료산화물을 대신하는 저가의 원료에 대한 요구가 당업계에는 존재하고 있었다.Accordingly, there is a need in the art for a low cost raw material instead of an expensive raw material oxide.
한편, 밀스케일은 철강제조공정, 특히 열간압연 또는 냉각작업 중에 강 표면에 생긴 산화물로서, 일반적으로 강에 접해있는 쪽으로부터 FeO, Fe3O4, Fe2O3의 순서로 형성되어 이루어지는 것으로 알려져 있다.On the other hand, the mill scale is an oxide formed on the surface of steel during the steel manufacturing process, especially hot rolling or cooling, and is known to be formed in the order of FeO, Fe 3 O 4 and Fe 2 O 3 from the steel contacting side. have.
이러한 밀스케일은 금속산화물임에도 불구하고 복상의 산화물들(FeO, Fe3O4, Fe2O3)로 이루어져 있어서 함께 혼합된 다른 금속산화물(예를 들면, NiO, CuO 등)과의 동시 환원이 어렵다는 한계를 가지고 있었다.Although the mill scale is a metal oxide, it is composed of a plurality of oxides (FeO, Fe 3 O 4 , Fe 2 O 3 ), so that simultaneous reduction with other metal oxides (eg, NiO, CuO, etc.) mixed together is prevented. It had a hard limit.
따라서, 본 발명의 목적은, 복상의 밀스케일을 단상화시킨 다음, 이를 다른 종류의 금속산화물과 혼합 및 분쇄한 후, 이를 수소환원시켜 양질의 나노분말로 제조하는 방법을 제공하는 것이다.Accordingly, it is an object of the present invention to provide a method for producing a high quality nanopowder by single phase of a multi-phase mill scale, then mixing and pulverizing it with another type of metal oxide, and then hydrogen reduction thereof.
도 1은 밀스케일을 열처리하는 동안 시간변화에 따른 Fe 산화물의 무게비 변화를 열분석법을 통해 측정하여 도시한 열분석 다이아그램.1 is a thermal analysis diagram showing the measurement of the change in the weight ratio of Fe oxide over time during the heat treatment of the mill scale through a thermal analysis method.
도 2a 및 도 2b는 각각 열처리전 밀스케일과 열처리후 밀스케일을 X-레이 회절분석하여 도시한 다이아그램.2A and 2B are diagrams showing X-ray diffraction analysis of mill scale before and after heat treatment, respectively.
도 3은 본 발명의 실시예 1에 따라 혼합된 밀스케일-NiO 혼합산화물을 100,000배 배율의 전자현미경으로 관찰한 사진.Figure 3 is a photograph of the mill scale-NiO mixed oxide mixed according to Example 1 of the present invention by electron microscope at a magnification of 100,000 times.
도 4a 및 도 4b는 실시예 1에 따라 제조되는 나노분말과 비교예 1에 따라 제조된 나노분말을 각각 200,000배 전자현미경으로 관찰한 사진.4A and 4B are photographs of the nanopowder prepared according to Example 1 and the nanopowder prepared according to Comparative Example 1, respectively, using 200,000-fold electron microscopes.
도 5는 본 발명의 실시예 1에 따라 제조되는 나노분말을 X-레이 회전분석하여 도시한 다이아그램Figure 5 is a diagram showing the X-ray rotation analysis of the nanopowder prepared according to Example 1 of the present invention
도 6은 본 발명의 실시예 1에 따라 제조된 나노분말을 VSM을 측정하여 그 결과를 도시한 다이아그램.Figure 6 is a diagram showing the results of measuring the VSM nanoparticles prepared according to Example 1 of the present invention.
상술한 목적을 달성하기 위해, 본 발명은 수집된 복상의 밀스케일을 대기중에서 열처리하여 단상화시키는 단계와, 단상화된 상기 밀스케일을 다른 종류의 금속산화물과 혼합하여 볼밀링 분쇄하는 혼합분쇄단계와, 상기 혼합분쇄단계를 통해 분말화된 혼합물을 수소분위기의 환원로 내에서 수소환원시키는 단계를 포함하는 것을 특징으로 나노분말 제조방법을 제공한다.In order to achieve the above object, the present invention comprises the step of heat-treating the collected multi-phase mill scale in the air in a single phase, and the mixed milling step of mixing the single-phased mill scale with other metal oxides and ball milling; It provides a method for producing nano-powder comprising the step of hydrogen reduction of the mixture powdered through the mixed grinding step in a reducing atmosphere of a hydrogen atmosphere.
이 때, 상기 열처리는 500℃ 이상으로 수행되는 것이 바람직한데, 500℃미만으로 열처리되는 경우 단상화 반응의 속도가 크게 지연될 수 있다.At this time, the heat treatment is preferably carried out at 500 ℃ or more, when the heat treatment is less than 500 ℃ may be greatly delayed in the rate of the single-phase reaction.
덧붙혀, 밀스케일의 주성분인 FeO, Fe3O4, Fe2O3는 모두 안정상인 Fe2O3로 변화되어 안정화되는 것이 일반적이지만, 밀스케일에 대해 상기의 열처리를 하지 않을 경우, 그 밀스케일은 Fe2O3로 안정화되는 기간이 너무 길어 실질적인 이용이 어렵다.Incidentally, the main components of mill scale, FeO, Fe 3 O 4 and Fe 2 O 3 are all changed to stable Fe 2 O 3 to stabilize, but if the above heat treatment is not performed on the mill scale, the mill The scale has a long period of stabilization with Fe 2 O 3 and is practically difficult to use.
또한, 상기 열처리, 특히 600℃ 이상의 가열처리는 밀스케일 내에 존재하는 불순물(예를 들면, Al, Si, Mn, Cr, K, Ca, Mg)을 승화시켜 보다 질 좋은 나노금속분말을 얻는 것을 가능하게 하는데, 특히, K, Ca, Mg 등의 저온 승화 금속은 거의 대부분 승화되어 제거된다.In addition, the heat treatment, in particular, the heat treatment of more than 600 ℃ can sublimate impurities (for example, Al, Si, Mn, Cr, K, Ca, Mg) present in the mill scale to obtain a higher quality nano metal powder. In particular, low-temperature sublimation metals such as K, Ca, and Mg are almost always sublimed and removed.
이하에서는, 본 발명의 바람직한 실시예 1이 상세하게 설명될 것이다.In the following, preferred embodiment 1 of the present invention will be described in detail.
<실시예 1><Example 1>
-철강제조공정에서 수집된 밀스케일 분말을 대기 중에서 800℃에서 3시간 가열처리 한 후, XRD와 EDS 분석을 통해 그 분말의 조성 및 상을 분석하였다.The mill scale powder collected in the steel manufacturing process was heat-treated at 800 ° C. for 3 hours in the air, and then the composition and phase of the powder were analyzed by XRD and EDS analysis.
-열처리한 밀스케일과 니켈산화물(NiO)을 Fe-50중량% Ni의 조성이 되도록 혼합물을 조성한 후, 탄소강 재질의 3mm 직경 볼 및 200㎖ 알콜계 용매가 넣어진 스테인레스강 재질의 2ℓ용적의 분쇄기(attritor) 내에 상기 혼합물을 장입하고 8시간 볼밀링을 실시했다.-Mix the heat-treated mill scale and nickel oxide (NiO) to a composition of Fe-50% by weight Ni, and then a 2 mill volume grinder made of stainless steel containing a 3 mm diameter ball made of carbon steel and 200 ml alcohol-based solvent. The mixture was charged in an attritor and ball milled for 8 hours.
-볼밀링된 혼합 산화물은 건조된 후 100메쉬에서 체질하여 분말상태로 만들어졌다.The ball milled mixed oxides were dried and sieved at 100 mesh to form a powder.
-상기 공정들을 거친 금속산화물의 혼합물은 600℃의 수소분위기 환원로 내에서 1시간 동안 수소환원되어 나노분말로 제조되었다.The mixture of the metal oxides subjected to the above processes was hydrogen-reduced for 1 hour in a hydrogen atmosphere reduction furnace at 600 ° C. to prepare nanopowders.
<시험예 1><Test Example 1>
도 1은 상기 실시예 1에 따라 밀스케일을 대기중에서 800℃의 온도로 열처리하는 과정 중에 그 열처리 시간에 따른 밀스케일 내의 Fe 산화물의 무게비 변화를 열분석법을 통해 측정하여 도시한 열분석(TG) 다이아그램이다.1 is a thermal analysis (TG) measured by measuring the weight ratio change of the Fe oxide in the mill scale according to the heat treatment time during the heat treatment of the mill scale to the temperature of 800 ℃ in the air according to Example 1 Diagram.
도 1은 열처리시, Fe 산화물의 무게비가 시간의 흐름에 따라 증가하고, 약 3시간(10000초)이 흐른 뒤에 그 무게비의 변화가 거의 없음을 나타낸다.FIG. 1 shows that during heat treatment, the weight ratio of Fe oxide increases with time, and there is little change in the weight ratio after about 3 hours (10000 seconds).
이러한 결과는 소정온도 및 소정의 시간으로 밀스케일을 가열처리하는 경우 밀스케일 내의 불순물, 특히 저온승화 금속성분들이 제거됨을 나타낸다.This result indicates that when the mill scale is heat-treated at a predetermined temperature and for a predetermined time, impurities in the mill scale, particularly low-temperature sublimation metal components, are removed.
<시험예 2><Test Example 2>
앞선 실시예 1에서, 열처리 되기 전의 밀스케일과 열처리된 후의 밀스케일을 각각 X레이 회절분석하였으며, 그 회절분석된 결과를 나타내는 다이아그램이 도 2a 및 도 2b에 각각 도시되어 있다.In Example 1, the mill scale before heat treatment and the mill scale after heat treatment were respectively analyzed by X-ray diffraction, and diagrams showing the results of the diffraction analysis are shown in FIGS. 2A and 2B, respectively.
도 2a를 참조하면, 열처리 되기 전의 밀스케일에는 α-Fe2O3, γ-Fe2O3및 FeO 상들이 혼재되어 있음을 알 수 있다.Referring to Figure 2a, it can be seen that the mill scale before the heat treatment is mixed α-Fe 2 O 3 , γ-Fe 2 O 3 and FeO phases.
반면, 도 2b를 참조하면, 열처리 된 후의 밀스케일에는 γ-Fe2O3만이 발견됨을 알 수 있다.On the other hand, referring to Figure 2b, it can be seen that only γ-Fe 2 O 3 is found in the mill scale after the heat treatment.
이를 통해, α-Fe2O3, γ-Fe2O3및 FeO로 복상을 이루던 열처리전의 밀스케일이 열처리후 α-Fe2O3로단상화되었음을 알 수 있었다.Through this, it can be seen that the mill scale before heat treatment, which was phased up with α-Fe 2 O 3 , γ-Fe 2 O 3, and FeO, was single-phased to α-Fe 2 O 3 after heat treatment.
<시험예 3><Test Example 3>
도 3은 앞선 실시예 1에 따라 밀스케일-NiO 혼합산화물을 볼밀링 한 후 주사전자현미경으로 관찰한 사진(배율:100,000배)이다.3 is a photograph (magnification: 100,000 times) observed with a scanning electron microscope after ball milling a millscale-NiO mixed oxide according to Example 1 above.
도 3을 참조하면, 밀스케일-NiO 혼합산화물이 볼밀링에 의해 극미세하게 분쇄되어 20~30㎚크기의 입자를 형성하고 있음을 알 수 있었고, 이를 통해, 볼밀에 의한 상기 혼합 산화물의 분쇄효과가 매우 큼을 알 수 있었다.Referring to FIG. 3, it can be seen that the mill scale-NiO mixed oxide is extremely finely ground by ball milling to form particles having a size of 20 to 30 nm, and through this, the grinding effect of the mixed oxide by the ball mill. Was found to be very large.
<비교예 1>Comparative Example 1
시약급의 Fe계 산화물 분말(Fe2O3)과 상기 실시예 1에서 이용된 것과 같은 니켈산화물(NiO)을 상기 실시예 1과 같은 조성(Fe-50중량% Ni)이 되게 혼합한 후 상기 실시예 1과 같은 조건으로 분쇄혼합 및 수소환원하여 나노분말을 제조하였다.Reagent grade Fe-based oxide powder (Fe 2 O 3 ) and nickel oxide (NiO) as used in Example 1 was mixed to the same composition as in Example 1 (Fe-50% by weight Ni) and then Nanopowders were prepared by pulverized mixing and hydrogen reduction under the same conditions as in Example 1.
<시험예 4><Test Example 4>
도 4a는 앞선 실시예 1에 따라 제조된 나노분말을 전자현미경으로 관찰한 사진(배율:20,000배)이며, 도 4b는 앞선 비교예 1에 따라 제조된 나노분말을 전자현미경으로 관찰한 사진(배율:20,000배)이다.4A is a photograph (magnification: 20,000 times) of the nanopowder prepared according to Example 1, followed by an electron microscope, and FIG. 4B is a photograph (magnification) of the nanopowder prepared according to Comparative Example 1 described above. : 20,000 times).
도 4a 및 도 4b를 참조하면, 실시예 1 및 비교예 1에 따라 각각 제조된 나노분말은 모두 100~200㎚의 응집체 크기를 가지고 있었으며, 특히, 상기 실시예 1 및 비교예 1에 따라 제조된 나노분말은 거의 동일한 미세조직과 입도분포를 가지고 있음을 알 수 있었다.4A and 4B, each of the nanopowders prepared according to Example 1 and Comparative Example 1 had an aggregate size of 100 to 200 nm, in particular, prepared according to Example 1 and Comparative Example 1 above. The nanopowders were found to have almost the same microstructure and particle size distribution.
<시험예 5><Test Example 5>
실시예 1에 따라 제조된 나노분말을 X레이 회절분석하였으며, 그 결과는 도 5에 도시되어 있다.Nanopowders prepared according to Example 1 were subjected to X-ray diffraction analysis and the results are shown in FIG. 5.
도 5에 도시된 바와 같이, 제조된 나노분말은 γ-Fe-Ni 합금상을 형성하고 있으며, 그 결정립의 크기는 약 20㎚이다.As shown in FIG. 5, the prepared nanopowder forms a γ-Fe—Ni alloy phase, and the grain size thereof is about 20 nm.
이러한 결과는 밀스케일이 γ-Fe-Ni 합금상을 형성하는데 있어 시약급의 Fe계 산화물을 대신할 수 있음을 보여준다.These results show that millscale can replace reagent grade Fe-based oxides to form γ-Fe-Ni alloy phases.
<시험예 6><Test Example 6>
실시예 1 및 비교예 1에 따라 제조된 나노분말에서의 불순물의 혼입정도가 EDS 성분분석에 의해 조사되었으며, 그 결과는 표 1에 각각 표시되었다.The degree of incorporation of impurities in the nanopowders prepared according to Example 1 and Comparative Example 1 was investigated by EDS component analysis, and the results are shown in Table 1, respectively.
상기 결과는, 실시예 1에 따라 제조된 나노분말에 있어서, 열처리 과정 동안 대부분의 저온승화금속 성분 불순물이 승화되어 제거되었음을 나타낸다.The results indicate that in the nanopowder prepared according to Example 1, most of the low temperature sublimed metal component impurities were sublimed and removed during the heat treatment process.
다만, 실시예 1의 나노분말에서는 비교예 1의 나노분말보다 많은 양이 Cr이 발견되었으나 실질적으로 나노분말의 물성에 큰 영향을 줄 정도는 아니었고, 나머지 미량 불순물들은 0.1 중량% 미만으로 측정되어, 실시예 1에 따라 제조된 나노분말이 비교예 1에 의해 제조되는 나노분말과 비교하여 그 불순물 함량에 있어서 큰 차이가 없음을 보였다.However, in the nanopowder of Example 1, Cr was found to be larger than the nanopowder of Comparative Example 1, but it was not enough to substantially affect the physical properties of the nanopowder, and the remaining trace impurities were measured to be less than 0.1 wt%. , The nanopowder prepared according to Example 1 showed no significant difference in its impurity content as compared with the nanopowder prepared according to Comparative Example 1.
<시험예 6><Test Example 6>
실시예 1에 따라 제조된 나노분말(조성=Fe-50중량% Ni)을 VSM으로 측정하고그 결과를 도 6의 다이아그램에 도시하였다.The nanopowder (composition = Fe-50 wt.% Ni) prepared according to Example 1 was measured by VSM and the results are shown in the diagram of FIG.
도 6으로부터, 그 히스테리시스 곡선이 전형적인 연자성체의 개형을 보임을 알 수 있었다. 또한, 그 포화자화값은 194 Oe, 그 보자력값은 104emu/g로 측정되어졌다.It can be seen from FIG. 6 that the hysteresis curve shows a typical soft magnetic remodeling. In addition, the saturation magnetization value was 194 Oe, and the coercive force value was measured to be 104 emu / g.
이러한 측정결과는 비교예 1에 의해 제조되는 나노분말과 동일한 것이며, 이는 실시예 1에 따라 제조된 나노분말이 상업적으로 이용되기에 충분하다는 것을 나타낸다.These measurement results are the same as the nanopowders prepared by Comparative Example 1, indicating that the nanopowders prepared according to Example 1 are sufficient for commercial use.
상술한 바와 같이, 본 발명은 값싼 밀스케일 원료를 이용해 높은 성능을 갖는 나노분말을 대량 제조할 수 있는 효과를 갖는다.As described above, the present invention has the effect of mass-producing nanopowders having high performance using inexpensive millscale raw materials.
또한, 본 발명은 차세대 첨단기술에서 요구되는 환경친화적인 공정 및 자원재활용을 동시에 충족할 수 있는 효과를 갖는다.In addition, the present invention has the effect of simultaneously meeting the environmentally friendly process and resource recycling required in the next-generation advanced technology.
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100766769B1 (en) * | 2005-09-16 | 2007-10-17 | 주식회사 이지 | Manufacture method of iron powder |
| KR101133659B1 (en) * | 2010-03-10 | 2012-04-10 | 티엔씨 주식회사 | Method of crushing zinc by-product by milling process and fine zinc powder crushed thereby |
| KR101400549B1 (en) * | 2012-07-25 | 2014-05-27 | 부경대학교 산학협력단 | the iron powder product method from forging scale |
| KR101897670B1 (en) * | 2017-04-28 | 2018-09-12 | 주식회사 솔루에타 | Method for manufacturing nickel nano power |
| WO2018199679A1 (en) * | 2017-04-28 | 2018-11-01 | 주식회사 솔루에타 | Method for preparing nickel nanopowders and method for making nickel nanopowders into paste |
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2003
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100766769B1 (en) * | 2005-09-16 | 2007-10-17 | 주식회사 이지 | Manufacture method of iron powder |
| KR101133659B1 (en) * | 2010-03-10 | 2012-04-10 | 티엔씨 주식회사 | Method of crushing zinc by-product by milling process and fine zinc powder crushed thereby |
| KR101400549B1 (en) * | 2012-07-25 | 2014-05-27 | 부경대학교 산학협력단 | the iron powder product method from forging scale |
| KR101897670B1 (en) * | 2017-04-28 | 2018-09-12 | 주식회사 솔루에타 | Method for manufacturing nickel nano power |
| WO2018199677A1 (en) * | 2017-04-28 | 2018-11-01 | 주식회사 솔루에타 | Method for producing nickel nanopowder |
| WO2018199679A1 (en) * | 2017-04-28 | 2018-11-01 | 주식회사 솔루에타 | Method for preparing nickel nanopowders and method for making nickel nanopowders into paste |
| KR20180121033A (en) * | 2017-04-28 | 2018-11-07 | 주식회사 솔루에타 | Method for manufacturing and paste nickel nano power |
| US11090722B2 (en) | 2017-04-28 | 2021-08-17 | Solueta Co., Ltd. | Method for preparing nickel nanopowders and method for making nickel nanopowders into paste |
| US11260452B2 (en) | 2017-04-28 | 2022-03-01 | Solueta Co., Ltd. | Method for producing nickel nanopowder |
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