Molybdenum, valued for its high melting point and exceptional physical and chemical properties, is studied in diverse fields such as electronics, petrochemicals, and aviation. Among molybdenum oxides, molybdenum dioxide stands out for its higher electrical conductivity than other transition metal oxides due to its structural characteristics, exhibiting metallic properties. It is applied as pellets to gas sensors, semiconductors, and secondary batteries for its properties. Thus, research on molybdenum dioxide compaction and pressureless sintering is necessary, yet research on pressureless sintering is currently insufficient. This study synthesized MoO₃ powder via solution combustion synthesis and reduced it using the 3% hydrogen/argon gas mixture to investigate the effect of reduction temperature on the powder. Additionally, the reduced powder was compacted and subjected to pressureless sintering with temperature as a variable. The density and the microstructure of brown parts were analyzed and discussed.

Molybdenum-tungsten (Mo-W) alloy sputtering targets are widely utilized in fields like electronics, nanotechnology, sensors, and as gate electrodes for TFT-LCDs, owing to their superior properties such as hightemperature stability, low thermal expansion coefficient, electrical conductivity, and corrosion resistance. To achieve optimal performance in application, these targets’ purity, relative density, and grain size of these targets must be carefully controlled. We utilized nanopowders, prepared via the Pechini method, to obtain uniform and fine powders, then carried out spark plasma sintering (SPS) to densify these powders. Our studies revealed that the sintered compacts made from these nanopowders exhibited outstanding features, such as a high relative density of more than 99%, consistent grain size of 3.43 μm, and shape, absence of preferred orientation.

Molybdenum is used in electrical contacts, industrial motors, and transportation materials due to its remarkable ability to resist heat and corrosion. It is also used to flame coat other metals. This study investigated, the thermal characteristics of the molybdenum sputtered material, such as electrical conductivity, and stealth effects on infrared thermal imaging cameras. To this end, molybdenum sputtered samples were prepared by varying the density of the base sample and the type of base materials used. Thereafter, the produced samples were evaluated for their surface state, electrical conductivity, electromagnetic field characteristics, thermal characteristics, stealth effect on infrared thermal imaging cameras, and moisture characteristics. As a result of infrared thermal imaging, the molybdenum layer was directed towards the outside air, and when the sample was a film, it demonstrated a greater stealth effect than the fabric. When the molybdenum layer was directed to the outside air, all of the molybdenum sputtering-treated samples exhibited a lower surface temperature than the “untreated sample.” In addition, as a result of confirming electrical properties following the molybdenum sputtering treatment, it was determined that the film exhibited better electrical conductivity than the fabric. All samples that were subjected to molybdenum sputtering exhibited significantly reduced electromagnetic and IR transmission. As a result, the stealth effect on infrared thermal imaging cameras is considered to be a better way of interpreting heat transfer than infrared transmission. These results are expected to have future applications in high-performance smartwear, military uniforms, and medical wear.

The molybdenum cup and molybdenum pin, which are the main materials of the molybdenum electrode used for the LCD BLU CCFL electrode, have not been developed in Japan and all of them are imported and used from Japan, is giving a competitive burden. In this research, to develop the manufacturing technology of molybdenum pin used for CCFL electrode of LCD BLU, development of linear processing technology, development of molybdenum wire surface treatment technology, development of wire cutting technology, production of molybdenum pin, design and fabrication of JIG and Fixture for inspection, molybdenum pin prototyping and analysis, and development of 100% molybdenum pin inspection technology. In this paper, especially, research on prototype manufacturing and CAE analysis is treated.

The molybdenum cup and molybdenum pin, which are the main materials of the molybdenum electrode used for the LCD BLU CCFL electrode, have not been developed in Japan and all of them are imported and used from Japan, is giving a competitive burden. In this research, the CCFL electrode of LCD BLU is used to develop the manufacturing technology of molybdenum pin. The development of linear processing technology is used to that. The development of molybdenum wire surface treatment technology is used to that. The development of wire cutting technology is ued to that. The design and fabrication of JIG and Fixture for inspection is used to that. The molybdenum pin prototyping and analysis is used to that and finally, the development of 100% molybdenum pin inspection technology is used to that. In this paper, especially, research on design technology of wire cutting is treated.

The molybdenum cup and molybdenum pin, which are the main materials of the molybdenum electrode used for the LCD BLU CCFL electrode, have not been developed in Japan and all of them are imported and used from Japan, is giving a competitive burden. In this research, to develop the manufacturing technology of molybdenum pin used for CCFL electrode of LCD BLU, development of linear processing technology, development of molybdenum wire surface treatment technology, development of wire cutting technology, production of molybdenum pin, design and fabrication of JIG and Fixture for inspection, molybdenum pin prototyping and analysis, and development of 100% molybdenum pin inspection technology. In this paper, especially, research on surface treatment technology of molybdenum wire is treated.

The molybdenum cup and molybdenum pin, which are the main materials of the molybdenum electrode used for the LCD BLU CCFL electrode, have not been developed in Japan and all of them are imported and used from Japan, is giving a competitive burden. In this research, to develop the manufacturing technology of molybdenum pin used for CCFL electrode of LCD BLU, development of linear processing technology, development of molybdenum wire surface treatment technology, development of wire cutting technology, production of molybdenum pin, design and fabrication of JIG and Fixture for inspection, molybdenum pin prototyping and analysis, and development of 100% molybdenum pin inspection technology. In this paper, especially, research on linear processing technology is treated.

몰리브덴-99의 붕괴에 의해 생산되는 테크네튬-99m 은 방사선 진단에 중요한 역할을 담당하고 있다. 몰리브덴-99 는 주로 우라늄-235의 핵분열에 의해 생산되고 있으며, 이를 위해 고농축 우라늄 표적 또는 저농축 우라늄 표적이 연구로에서 조사 된다. 현재는 고농축 우라늄의 사용에 따른 핵확산 문제를 저감하기 위해 저농축 우라늄 표적의 사용이 권장되고 있다. 본 연구는 몰리브덴-99 생산 시설의 계획 단계에서 방사성 폐기물 관리 전략을 정의하기 위하여 저농축 우라늄의 사용이 방사 성 폐기물의 흐름에 미치는 영향을 분석하였다. 저농축 우라늄 표적 사용 시 우라늄 함유 폐기물의 부피가 6배 이상 증가하 기 때문에 우라늄 고밀도 표적의 사용과 고온 정수압 압축법의 활용이 제안되었다.

Mo nanopowder was synthesized by ball-milling and subsequent hydrogen-reduction of powder. To fabricate ultra fine grained molybdenum, two-step sintering and spark plasma sintering process were employed. The grain size of specimen by two-step sintering and spark plasma sintering was around and , respectively. Mechanical properties of ultra fine grained Mo with relative density of above 90% were significantly improved at room and high temperatures comparing to commercial bulk Mo of 99% relative density. This result was mainly explained by the grain size refinement due to diffusion-controlled sintering.

Iron(Fe)-Molybdenum(Mo) alloyed nanoparticles and nanowires were produced by the chemical vapor condensation(CVC) process using the pyrolysis of iron pentacarbonyl() and Molybdenum hexacarbonyl(). The influence of CVC parameter on the formation of nanoparticle, nanowire and size control was studied. The size of Fe-Mo alloyed nanoparticles can be controlled by quantity of gas flow. Also, Fe-Mo alloyed nanowires were produced by control of the work chamber pressure. Moreover, we investigated close correlation of size and morphology of Fe-Mo nanoparticles and nanowires with atomic quantity of inflow precursor into the electric furnace as the quantitative analysis. Obtained nanoparticles and nanowires were investigated by field emission scanning electron microscopy, energy dispersive spectroscopy and X-ray diffraction.

Froth flotation has been carried out in order to produce roasting-molybdenite concentrate from molybdenite ore in the Shin-yeomi mine. In our study, roasting-molybdenite (Mo 0.43%) from Shin-yeomi mine was recovered by varying the conditions of regrinding time, dosage of collector and alkalinity. Liberation and flotation efficiency more were effective at regrinding time of six minutes than at single grinding. Mo recovery curves increased considerably as dosage of kerosene increased, whereas Mo grade curves decreased gradually. The separation efficiency of molybdenite was effective when the dosage of collector (kerosene) was adjusted to 300 g/t. The molybdenite concentrate was agglomerated in the range of pH 5-7 and its separation efficiency increased to pH 9-10. The concentrate of 49.5% Mo grade (MoS2, 82.6%) with 81.5% recovery from Shin-yeomi molybdenite ores was obtained under conditions of 20% pulp concentration, 300 g/t kerosene 325 g/t frother (AF65), 2.5 kg/t depressant (Na2SiO3), pH 9-10 and four cleaning times. In the future, a trial run that can separate up to 50% Mo grade from Shin-yeomi molybdenite ores will be performed.

It is interesting to discover the reaction kinetics of the newly developed molybdenum containing catalysts. The dissociation/adsorption of nitrogen on molybdenum surface is known to be structure sensitive, which is similar to that of nitrogen on iron surface. The rates over molybdenum nitride catalysts are increased with the increase of total pressure. This tendency is the same as that for iron catalyst, but is quite different from that for ruthenium catalyst. The activation energies of the molybdenum nitride catalysts are almost on the same level, although the activity is changed by the addition of the second component. The reaction rate is expressed as a function of the concentration of reactants and products. The surface nature of CO3Mo3N is drastically changed by the addition of alkali, changing the main adsorbed species from NH2 to NH on the surface. The strength of NHx adsorption is found to be changed by alkali dopping.

The Mo(V) di-μ-oxo type [Mo2O4(H2O)2L2] SO4 complexes(L: 2,2'-dipyridyl,4,4'-ethylenedianlline) have been prepared by the reaction of [Mo2O4(H2O)6]SO4 with a series of chelate ligands. These complexes are completed by two terminal oxygens arranged trans to one another and each ligand forms a chelate types. In Mo2O4(H2O)2L2, two H2O coordinated at trans site of terminal oxygens. The prepared complexes have been characterized by elemental analysis, infrared spectra, 1H nuclear magnetic resonance spectra, and thermal analysis(TG-DTA). In the potential range -0.00V to -1.00V at a scan rate of 50mVs-1, a cathodic peak at -0.81V ~ -0.87V (vs SCE) and an anodic peak at -0.61V ~ -0.63V (vs SCE) have been observed in aquous solution. We infer these redox are irreversible reaction.

자전고온합성반응법을 이용하여 이규화 몰리브덴-텅스텐(Mo1-z , Wz)Si2을 합성하였다. 조성 (z)을 변화시켜 성형한 원통형 시편에 합성반응 중 전달되는 온도변화를 예측하기 위하여 시편의 중앙에 열전대를 삽입하였다. 반응 선단면이 열전대를 통과할 때 가장 높은 반응온도를 보이고 이것을 단열반응 온도라 간주하였다. 따라서 본 연구에서는 이러한 온도변화를 예측하기 위하여 자전조온합성반응의 모델링을 계시하고자 하였으며, 실험을 통하여 측정한 반응온도 분포곡선의 거동을 비교하였다. 각각의 시료에 대한 실험결과 측정된 반응속도는 약 2.14~1.35mm/sec, 반응온도는 1883K~1507K의 간을 보였다. 두 항 모두 텅스텐의 함량이 증가함에 따라 감소하는 경향을 나타냈으며, 수치해석을 통하여 거의 유사한 반응온도를 얻었다. 시료의 초기온도를 증가시킬 경우 반응온도는 증가함이 예측되었고, z=0.5인 시료에 대하여 반응온도가 1900k 이상이 되기 위해서는 약 800K-900K의 예열이 필요하였다.

The Mo(V) di-μ-oxo type [Mo2O4(H2O)2L]Cl2 complexes(L: 4,4'-Diphenyl-2,2'-dipyridyl, 4,4'-Dimethyl-2,2'-dipyridyl, 4,7-Diphenyl-1,10-phenanthroline) have been prepared by the reaction of [Mo2O4(H2O)6]2+ with a series of chelate ligands. These complexes are completed by two terminal oxygens arranged trans to one another and each ligand forms a chelate types. In Mo2O4(H2O)2L two H2O coordinated at trans site of terminal oxgens. The prepared complexes have been characterized by elemental analysis, infrared spectra, electronic spectra, 1H nuclear magnetic resonance spectra, and thermal analysis(TG-DTA). In the potential range -0.00V to -1.00V at scan rate of 50mVs-1, a cathodic peak at -0.83V ~ -0.88V (vs SCE) and an anodic peak at -0.54V ~ -0.88V (vs SCE) have been observed in aquous solution. The ratio of the cathodic to anodic current(Ipc/Ipa) is almost 2, we infer that redox is irreversible as dimer forms broken.