2022년 기준 국내 폐타이어 발생량은 약 37만톤으로 그 중 88.9%인 약 32만 9천톤이 재활용되는 것으로 조사되었다. 하지만 이 중 약 75%가 시멘트소성로용 등 열이용 분야에 사용되었다. 폐타이어는 대부분 고무와 플라스틱으로 이루어져 있기 때문에, 고온에서 분 해되면서 다양한 유해가스와 오염물질이 발생할 수 있고, 이러한 공해물질은 적극적으로 관리되지 않으면 대기오염, 수질 오염 등 다 양한 환경문제를 발생시킬 수 있다. 때문에 친환경적이고 지속적인 재활용에 대한 필요성이 대두되고 있다. 폐타이어 고무 분말을 아스팔트 혼합물의 골재 일부로 치환하여 재활용하는 접근 방식은 환경에 미치는 영향을 완화할 뿐만 아니라 천연 자원의 고갈 측면에서도 긍정적인 영향을 미치는 것으로 판단된다. 따라서 타이어분말을 아스팔트 혼합물에 적용하는 것은 환경 문제를 해결하고 자원 효율성을 높이는 두 가지 이점을 가지고 있다. 폐타이어 분말을 아스팔트 바인더와 아스팔트 혼합물에 적용할 경우 미치는 영향을 평가하기 위하여 DSR, BBR, MSCR 등의 시험 을 진행하였으며, 아스팔트 혼합물 내 폐타이어 분말의 분포를 조사하기 위해 SEM을 실시하였다. 또한 IDEAL-CT와 IDEAL-Rutting 시 험을 통해 아스팔트 혼합물의 성능을 평가하였다.

W2C is synthesized through a reaction-sintering process from an ultrafine-W and WC powder mixture using spark plasma sintering (SPS). The effect of various parameters, such as W:WC molar ratio, sintering temperature, and sintering time, on the synthesis behavior of W2C is investigated through X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) analysis of the microstructure, and final sintered density. Further, the etching properties of a W2C specimen are analyzed. A W2C sintered specimen with a particle size of 2.0 μm and a relative density over 98% could be obtained from a W-WC powder mixture with 55 mol%, after SPS at 1700℃ for 20 min under a pressure of 50 MPa. The sample etching rate is similar to that of SiC. Based on X-ray photoelectron spectroscopy (XPS) analysis, it is confirmed that fluorocarbon-based layers such as C-F and C-F2 with lower etch rates are also formed.

This study evaluated effects of the addition of garlic powder allicin (GPA) mixture on rumen fermentation with methane in Hanwoo steer. On in vitro trial, two experimental groups were used: control (without GPA) and treatment group (addition of 0.1% GPA mixed with the basal concentrate). Similar to in vitro trial, two experimental groups were used in vivo trial. Five Hanwoo steers (3 steers in one group and 2 in another group; average body weight = 500 ± 43 kg) were assigned by crossover design for 20 d consists of 15 d diet adaptation and 5 d data collection in each experimental period. Daily feed intake and enteric methane production were recorded by an automated head chamber system. The results of in vitro study showed that the GPA treatment group had higher acetic acid (24.30 vs 23.45 mmol/L) and butyric acid (16.55 vs 15.47 mmol/L) concentrations, but lower CH4 production (1.40 vs 2.71 mmol/ml) after 24 h of incubation compared to the control (p<0.05). Total gas, propionic acid, total volatile fatty acid (VFA), and acetic acid: propionic acid ratio were not affected by treatment after 24 h incubation. In the in vivo experiment, rumen pH and VFA were not significantly different between treatments (p>0.05), except acetic acid, which was significantly higher in GPA mixture group (60.97 vs 53.94 mM) than in the control group (p<0.05). Furthermore, no significant differences were recorded in CH4 production (g/d) and CH4 yield (g/kg DMI) between the two groups (p>0.05). In conclusion, the addition of 0.1% GPA mixture reduced CH4 proudcition on in vitro trial, but no effect on in vivo trial.

ZnO crystals with different morphologies are synthesized through thermal evaporation of the mixture of Zn and Cu powder in air at atmospheric pressure. ZnO crystals with wire shape are synthesized when the process is performed at 1,000 oC, while tetrapod-shaped ZnO crystals begin to form at 1,100 oC. The wire-shaped ZnO crystals form even at 1,000 oC, indicating that Cu acts as a reducing agent. As the temperature increases to 1,200 oC, a large quantity of tetrapod-shaped ZnO crystals form and their size also increases. In addition to the tetrapods, rod-shaped ZnO crystals are observed. The atomic ratio of Zn and O in the ZnO crystals is approximately 1:1 with an increasing process temperature from 1,000 oC to 1,200 oC. For the ZnO crystals synthesized at 1,000 oC, no luminescence spectrum is observed. A weak visible luminescence is detected for the ZnO crystals prepared at 1,100 oC. Ultraviolet and visible luminescence peaks with strong intensities are observed in the luminescence spectrum of the ZnO crystals formed at 1,200 oC.

This study was performed to evaluate the quality characteristics of functional Dasik prepared with a mixture of freeze-dried mealworm (Tenebrio molitor) powder and dried pollack powder along with assessment of the general and fatty acid compositions of mealworms. General compositions, except for moisture content of freeze-dried mealworm powder, were higher than those of raw mealworms. The ratios of saturated fatty acids and unsaturated fatty acids of freeze-dried mealworm powder and raw mealworms were 1:3.31 and 1:3.19, respectively. Amounts of oleic acid, which was the most abundant among unsaturated fatty acids, of freeze-dried mealworm powder and raw mealworms were 41.12 and 37.84%, respectively. For color values, greater content of freeze-dried mealworm powder in functional Dasik resulted in lower L and b scores, whereas a value increased. In the case of mechanical properties, greater content of freeze-dried mealworm powder resulted in significant reduction of hardness, chewiness, and gumminess. In the case of sensory evaluation, color, taste, and overall quality of DPMD50, which was prepared with a 1:1 ratio of freeze-dried mealworm powder and dried pollack, were the highest. It was concluded that DPMD50 is a nutritious combination of edible insects and fish for protein fortification for growth and the elderly.

A Nanosized WO3 and CuO powder mixture is prepared using novel high-energy ball milling in a bead mill to obtain a W-Cu nanocomposite powder, and the effect of milling time on the structural characteristics of WO3-CuO powder mixtures is investigated. The results show that the ball-milled WO3-CuO powder mixture reaches at steady state after 10 h milling, characterized by the uniform and narrow particle size distribution with primary crystalline sizes below 50 nm, a specific surface area of 37 m2/g, and powder mean particle size (D50) of 0.57 μm. The WO3-CuO powder mixtures milled for 10 h are heat-treated at different temperatures in H2 atmosphere to produce W-Cu powder. The XRD results shows that both the WO3 and CuO phases can be reduced to W and Cu phases at temperatures over 700oC. The reduced W-Cu nanocomposite powder exhibits excellent sinterability, and the ultrafine W-Cu composite can be obtained by the Cu liquid phase sintering process.

A sintered body of TiB2-reinforced iron matrix composite (Fe-TiB2) is fabricated by pressureless-sintering of a mixture of titanium hydride (TiH2) and iron boride (FeB) powders. The powder mixture is prepared in a planetary ball-mill at 700 rpm for 3 h and then pressurelessly sintered at 1300, 1350 and 1400oC for 0-2 h. The optimal sintering temperature for high densities (above 95% relative density) is between 1350 and 1400oC, where the holding time can be varied from 0.25 to 2 h. A maximum relative density of 96.0% is obtained from the (FeB+TiH2) powder compacts sintered at 1400oC for 2 h. Sintered compacts have two main phases of Fe and TiB2 along with traces of TiB, which seems to be formed through the reaction of TiB2 formed at lower temperatures during the heating stage with the excess Ti that is intentionally added to complete the reaction for TiB2 formation. Nearly fully densified sintered compacts show a homogeneous microstructure composed of fine TiB2 particulates with submicron sizes and an Fe-matrix. A maximum hardness of 71.2 HRC is obtained from the specimen sintered at 1400oC for 0.5 h, which is nearly equivalent to the HRC of conventional WC-Co hardmetals containing 20 wt% Co.

Fe-30 wt% TiC composite powders are fabricated by in situ reaction synthesis after planetary ball millingof (Fe, TiH2, Carbon) powder mixture. Two sintering methods of a pressureless sintering and a spark-plasma sinteringare tested to densify the Fe-30 wt% TiC composite powder compacts. Pressureless sintering is performed at 1100, 1200and 1300oC for 1-3 hours in a tube furnace under flowing argon gas atmosphere. Spark-plasma sintering is carried outunder the following condition: sintering temperature of 1050oC, soaking time of 10 min, sintering pressure of 50 MPa,heating rate of 50oC/min, and in a vacuum of 0.1 Pa. The curves of shrinkage and its derivative (shrinkage rate) areobtained from the data stored automatically during sintering process. The densification behaviors are investigated fromthe observation of fracture surface and cross-section of the sintered compacts. The pressureless-sintered powder com-pacts are not densified even after sintering at 1300oC for 3 h, which shows a relative denstiy of 66.9%. Spark-plasmasintering at 1050oC for 10 min exhibits nearly full densification of 99.6% relative density under the sintering pressure of50 MPa.

This study was performed to produce WBM (wheat and barley mixture) bread containing molokhia powder with quality characteristics and antioxidant activities. Analysis of the chromaticity of WBM prepared with molokhia powder showed that; the lightness and redness were decreased, but yellowness was increased. In mechanical properties, hardness, gumminess, and chewiness were significantly increased as the amount of molokhia powder was increased. However, cohesiveness was significantly decreased. In sensory evaluation, WBM bread containing 1.5% of molokhia powder (MB1.5) showed an overall high preference level. The total polyphenol content of molokhia powder EtOH extract and MB1.5 were 29.19 and 58.18 mg TAE/g, respectively. The total flavonoid contents of molokhia powder EtOH extract and MB1.5 were 20.62 mg and 33.25 mg RE/g, respectively. The radical scavenging ability (IC50) of DPPH (IC50) for molokhia powder EtOH extract and MB1.5 was 31.04 and 58.18 μg/mL, respectively while that of ABTS was 33.25 and 54.15 μg/mL, respectively. The α -glucosidase inhibitory effects of molokhia powder EtOH extract and MB1.5 were 494.88 and 814.88 μg/mL, respectively. MB bread containing 1.5% molokhia powder showed antioxidative effects and α-glucosidase inhibitory activity, meaning that not only molokhia but also MB1.5 bread has the potential to prevent chronic degenerative diseases such as diabetes.

High temperature plasma coating technology has been applied to recover damaged aluminum dies from wear by spraying pure aluminum and alumina powder. However, the coated mixed powder layer composed of aluminum and alumina often undergoes a detachment from the substrate, making the coated substrate die unable to maintain its expected life span. In this study, in order to increase the bonding strength between the substrate and the coating layer, a pure aluminum layer was applied as an intermediate bond layer. In order to prepare the specimen with variable bond coating conditions, the bond coat layers with a various gun speed from 10 cm/sec to 30 cm/sec were prepared with coating cycle variations ranging from three to nine cycles. The specimen with a bond coat layer coated with a gun speed of 20 cm/sec and three coating cycles exhibited ~13MPa of adhesion strength, while the specimen without a bond coat layer showed ~6 MPa of adhesion strength. The adhesion strength with a variation of bond coat layer thickness is discussed in terms of coating parameters.

Translucent alumina is a potential candidate for high temperature application as a replacement of the glassor polymer. Recently, due to the increasing demand of high power light emitting diode (LED), there is a growing inter-est in the translucent alumina. Since the translucent property is very sensitive to the internal defect, such as voids insideor abnormal grain growth of sintered alumina, it is important to fabricate the defect-free product through the fabricationprocess. Powder injection molding (PIM) has been commonly applied for the fabrication of complex shaped products.Among the many parameters of PIM, the flowability of powder/binder mixture becomes more significant especially forthe shape of the cavity with thin thickness. Two different positions of the gate were applied during PIM using the disctype of die. The binder was removed by solvent extraction method and the brown compact was sintered at 1750oC for3 hours in a vacuum. The flowability was also simulated using moldflow (MPI 6.0) with two different types of gate.The effect of the flowability of powder/binder mixture on the microstructure of the sintered specimen was studied withthe analysis of the simulation result.

Cu-Ni alloys with unidirectionally aligned pores were prepared by freeze-drying process of CuO-NiO/cam-phene slurry. Camphene slurries with dispersion stability by the addition of oligomeric polyester were frozen at -25˚C,and pores in the frozen specimens were generated by sublimation of the camphene during drying in air. The green bod-ies were hydrogen-reduced at 300˚C and sintered at 850˚C for 1h. X-ray diffraction analysis revealed that CuO-NiOcomposite powders were completely converted to Cu-Ni alloy without any reaction phases by hydrogen reduction. Thesintered samples showed large and aligned parallel pores to the camphene growth direction, and small pores in the inter-nal wall of large pores. The pore size and porosity decreased with increase in CuO-NiO content from 5 to 10 vol%.The change of pore characteristics was explained by the degree of powder rearrangement in slurry and the accumulationbehavior of powders in the interdendritic spaces of solidified camphene.

Nanocrystalline powder could be synthesized by solid-state reaction using the mixture which was prepared by a high energy milling process in a bead mill for and nanocrystalline powders mixture. Effect of the milling time on the powder characteristic of the synthesized powder was investigated. Nanocrystalline with a particle size of 50 nm was obtained at . High tetragonal powder with a tetragonality(=c/a) of 1.009 and a specific surface area of was acquired after heat-treatment at for 2 h. High energy ball milling was effective in decreasing the reaction temperature and increasing the tetragonality.

3-D shape soft magnetic composite parts can be formed by general compaction method of powder metallurgy. In this study, the results on the high density nanostructured Fe-Si/Fe composite prepared by a warm compaction method were presented. Ball-milled Fe-25 wt.%Si powder, pure Fe powder and Si-polymer were mixed and then the powder mixture was compacted at various temperatures and pressures. Pore free density of samples up to 95% theoretical value has been obtained. The warm compacted sample prepared at 650 MPa and 240℃ had highest compaction properties in comparison with other compacts prepared at 300, 400 MPa and room temperature and 120℃. The magnetic properties such as core loss, magnetization saturation and coercivity were measured by B-H curve analyzer and vibration sample magnetometer.

In the present work, the influence of the ball-milling time, milling atmosphere and weight ratio of ball to powder on characteristics of was studied. Results show that, the grain sizes of the and CuO in the ball-milled powder mixture were significantly decreased with increasing the milling time. Those of each oxide ball-milled in Argon and Hexane atmosphere for 30 and 20 hour were about 98 and 84 nm, respectively. After milling of 20 hour in Hexane as PCA, the powder had a homogeneously mixed structure and the average size of powders was determined to about 230nm.

Recently warm compaction techniques are focused on and commercialization of one high-density compaction process in the P/M industry. Another development is a new SEGLESS using a developed lubricant that reduces ejection force at room temperature compaction. It is possible to achieve high-density by reducing lubricant amount. In this paper we confirmed that green density was 7.35 g/cm3 at 686MPa of compaction pressure when the new SEGLESS was applied to relatively lower temperature warm compaction process, such as 80℃.