기존의 사후경과시간(PMI) 추정 방법은 대략적인 사후경과시간의 추정, 사후 48~72시간 경과 또는 부패 시 추정 불가능이라는 문제가 발생하여 최근에는 법의곤충학(Medicolegal entomology)을 통한 최소 사후 경과시간 (PMImin) 추정이 더욱 강조되고 있다. 이로 인해 시식성파리의 발육 성장속도 파악은 시체의 최소 사후 경과시간 추정에 있어 효과적인 도구로 활용될 수 있다. 본 연구에서는 곱슬털쉬파리(Parasarcophaga. similis)를 사육대상 종으로 선정하였다. P. similis는 부패한 시체를 섭식하는 시식성파리 중 하나로서, 발육 성장 속도에 따른 법곤충 학적(Forensic entomology) 최소 사후 경과시간을 추정하는 데 중요한 지표가 된다. 실험에 사용된 대상종의 경우, 경북 칠곡군 지천면 일대에서 6~9월경 야외쉬파리 채집하였고, 종 동정, 사육 및 증식, 예비 실험을 거친 후 본실험 을 진행하였다. 본실험은 산란 집단 케이지 내에서 산란 유도 후 12시간 간격으로 6개체를 샘플링하였고, 이를 Leica M125 Microscope (Leica Microsystems, Germany), EG-2HDNL(이지테크, Korea)로 이미지와 측정치를 확보 하였다. P. similis를 16~34°C 사이 7개의 온도 조건에서 성장 속도 측정을 3회 반복 실험하였으며, 곱슬털쉬파리의 최초 출현시점, 특정 온도 조건 별 발육 성장 속도 측정, 유충 몸길이 데이터, 이미지 자료, 표본 등을 확보하였다. 16, 19, 22, 25, 28, 31, and 34°C에서 P. similis의 알에서 성충까지의 발달 기간은 각각 822.0±5.9, 605.0±12.2, 442.3±9.4, 339.3±6.1, 289.3±7.5, 253.0±8.0, and 248.7±3.4h이 경과함을 확인하였다. 본 연구의 결과는 P. similis의 성장과정 데이터와 PMImin추정을 위한 지표로서 활용가능한 데이터를 제공한다.

Abstract Y2Ti2O7 nanoparticles (0.3 mol%) have been successfully synthesized by the co-precipitation process. The samples, adjusted to pH7 with ammonia solution as catalyst and calcined at 700~900 ℃, exhibit very fine particles with close to spherical shape and average size of 10-30 nm. It was possible to control the size of the synthesized Y2Ti2O7 particles by manipulating the conditions. The Y2Ti2O7 nanoparticles were coated on a glass substrate by a dipping coating process with inorganic binder. The Y2Ti2O7 solution coated on the glass substrate had excellent adhesion of 5B; pencil hardness test results indicated an excellent hardness of 6H. The thickness of the thick film was about 30 μm. Decomposition of MB on the Y2Ti2O7 thin film shows that the photocatalytic properties were excellent.

Nickel powders were prepared under solvothermal condition by precipitation from metal nitrates with aqueous ammonium hydroxide. The powders were obtained at in a temperature range of 190-250 oC for 6h. The morphology and size of nickel powders were studied as a function of reaction temperature. The synthesis of nickel crystalline particles is possible under a solvothermal conditions in ethylene glycol solution. Characterization of the synthesized nickel powders were studied by XRD, SEM(FE-SEM) and TG/DSC. X-ray diffraction analysis of the synthesized powders indicated the formation of nickel structure after reaction. The average crystalline sizes of the synthesized nickel powders were in the range of 200-1000 nm; and the distribution of the powders was broad. The shape of the synthesized nickel particles was almost spherical. The morphology of synthesized nickel powders changed with reaction condition. It was possible to synthesize nickel powders directly in ethylene glycol without reducing agent.

In this study, the properties of Ag-coated TiO2 nanoparticles were observed, while varying the molar ratio of water and Ag+ for the surfactant and TiO2. According to the XRD results, each nanoparticle showed a distinctive diffraction pattern. The intensity of the respective peaks and the sizes of the nanoparticles increased in the order of AT1(R1 = 5)(33.3 nm), AT2 (R1 = 10)(38.1 nm), AT3(R1 = 20)(45.7 nm), AT4(R1 = 40)(48.6 nm) as well as AT5(R2 = 0.2, R3 = 0.5)(41.4 nm), AT6(R2 = 0.3, R3 = 1)(45.1 nm), AT7(R2 = 0.5, R3 = 1.5)(49.3 nm), AT8(R2 = 0.7, R3 = 2)(57.2 nm), which values were consistent with the results of the UV-Vis. spectrum. The surface resistance of the conductive pastes fabricated using the prepared Ag-coated TiO2 nanoparticles exhibited a range 7.0~9.0(274~328 μΩ/cm2) times that of pure silver paste(ATP)(52 μΩ/cm2).

Using reverse micelle processing, ZnAl2O4 nanopowders were synthesized from a mixed precursor(consisting of Zn(NO3)2 and Al(NO3)3). The ZnAl2O4 was prepared by mixing the aqueous solution at a molar ratio of Zn : Al = 1 : 2. The average size and distribution of the synthesized powders with heat treatment at 600 oC for 2 h were in the range of 10-20 nm and narrow, respectively. The average size of the synthesized powders increased with increasing water to surfactant molar ratio. The XRD diffraction patterns show that the phase of ZnAl2O4 was spinel(JCPDS No. 05-0669). The synthesized and calcined powders were characterized using a thermogravimetric - differential scanning calorimeter(TG-DSC), X-ray diffraction analysis (XRD), and high resolution transmission electron microscopy(HRTEM). The effects of the synthesis parameter, such as the molar ratio of water to surfactant, are discussed.

NiAl2O4 nanoparticle was synthesized by a reverse micelle processing for inorganic pigment. N (NO3)2·6H2O and Al(NO3)3·9H2O were used for the precursor in order to synthesize NiAl2O4 nanoparticles. The aqueous solution, which consisted of a mixing molar ratio of Ni/Al, was 1:2 and heat treated at 800~1100 oC for 2h. The average size and distribution of synthesized NiAl2O4 powders are in the range of 10-20 nm and narrow, respectively. The average size of the synthesized NiAl2O4 powders increased with an increasing water-to-surfactant molar ratio and heating temperature. The crystallinity of synthesized NiAl2O4 powder increased with an increasing heating temperature. The synthesized NiAl2O4 powders were characterized by X-ray diffraction analysis(XRD), a field emission scanning electron microscop (FE-SEM), and a color spectrophotometer. The properties of synthesized powders were affected as a function such as a molar ratio and heating temperature. Results indicate that synthesis using a reverse miclle processing is a favorable process to obtain NiAl2O4 spinels at low temperatures. The procedure performed suggests that this new synthesis route for producing these oxides has the advantage of being fast and simple. Colorimetric coordinates indicate that the pigments obtained exhibit blue colors.