목적 : 라식수술 후 고위수차에 영향을 미치는 요인을 분석하였다. 방법 : 기존의 라식수술을 받은 42안(23.43±2.06세)을 대상으로 하였고, 눈의 고위수차는 파면수차계를 이용하여 측정하였다. 라식수술안의 고위수차에 대한 모든 독립변수들의 기여도는 단순선형회귀분석과 다중회귀분석을 이용하여 평가하였다. LASIK 대상자의 전체고위수차에 영향을 미치는 요인을 평가하기 위해 후진선택방법의 다중회귀분석이 사용되었다. 결과 : 라식수술 대상자에서 전체고위수차의 RMS 값은 4 mm 동공에서 0.121±0.050, 6 mm 동공에서는 0.570±0.260였다. 다중회귀분석에서 4 mm 동공의 전체고위수차와 관련 있는 변수는 각막절제직경과 OSI이었고, 6 mm 동공에서 전체고위수차와 관련 있는 변수는 각막두께, 각막절삭량, 각막절제직경, LCVA(photopic), HCVA(mesopic), MTF cutoff 등으로 나타났다. 최종 다중회귀모델에서, 4 mm 동공의 전체고위수차에 유의하 게(p<0.050) 영향을 미치는 변수는 OSI(p=0.036)로 나타났고, 6 mm 동공의 전체고위수차에 유의하게 영향을 미치는 변수는 각막절삭량(p=0.016), HCVA(mesopic)(p=0.002), MTF cutoff(p=0.039) 등으로 나타났다. 결론 : 본 연구의 결과는 라식수술 후 변화된 각막형상으로 증가된 고위수차가 눈의 광학적 시스템에 영향을 미치면서 시력의 질에 영향을 줄 수 있음을 시사한다.

This research aims to study the simultaneous extraction and transesterification of Chlorella vulgaris (C. vulgaris) using microwave irradiation with methanol as solvent and potassium hydroxide (KOH) as catalyst. The microwave-assisted insitu transesterification of C. vulgaris is assessed at various ratios of biomass-to-methanol, reaction times, and catalyst concentrations during the centrifugation and evaporation process. Gas chromatography-mass spectrometry (GC-MS) analysis is performed to confirm fatty acid methyl ester (FAME) composition. Biodiesel preparation is carried out by simultaneous extraction and transesterification of microalgae from C. vulgaris. The product is then characterized using Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance (1H-NMR); microalgae are observed using scanning electron microscopy (SEM). The highest amount of FAME is obtained at a biomass-to-methanol ratio of 1:12, reaction time of 40 min, and catalyst concentration of 2 wt%. Biodiesel shows conversion to about 77.64% of methyl ester (methyl myristate, methyl palmitoleate, methyl linoleate, methyl oleate, methyl arachidonate, and methyl 5,8,11,14,17-eicosapentanoate).

In-situ carbon-coated tin oxide (ISCC-SnO2) was fabricated by colloidal processing and sucrose was used as a soluble carbon source. ISCC-SnO2 was characterized by X-ray diffraction (XRD), Raman spectroscopy, and nitrogen adsorption–desorption by BET methods, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) properties of ISCC-SnO2 were investigated in 1 M Na2SO4 solution. The specific capacitance of ISCC-SnO2 was achieved 42.7 mFcm−2 at a scan rate of 25 mVs−1 and showed excellent charge–discharge behavior.

For solving phase separation of nanoparticles and graphene oxide (GO) in the application process, MgWO4– GO nanocomposites were successfully synthesized using three different dispersants via a facile solvothermal-assisted in situ synthesis method. The structure and morphology of the prepared samples were characterized by X-ray diffraction, Scanning electron microscopy, Transmission electron microscopy, Fourier transform infrared and Raman techniques. The experimental results show that MgWO4 nanoparticles are tightly anchored on the surfaces of GO sheets and the agglomeration of MgWO4 nanoparticles is significantly weakened. Additionally, MgWO4– GO nanocomposites are more stable than self-assembly MgWO4/ GO, which there is no separation of MgWO4 nanoparticles and GO sheets by ultrasound after 10 min. The catalytic results show that, compared with bare MgWO4, MgWO4– GO nanocomposites present better catalytic activities on the thermal decomposition of cyclotetramethylenete tranitramine (HMX), cyclotrimethylene trinitramine (RDX) and ammonium perchlorate (AP). The enhanced catalytic activity is mainly attributed to the synergistic effect of MgWO4 nanoparticles and GO. MgWO4– GO prepared using urea as the dispersant has the smallest diameter and possesses the best catalytic action among the three MgWO4– GO nanocomposites, which make the decomposition temperature of HMX, RDX and AP reduce by 10.71, 11.09 and 66.6 °C, respectively, and the apparent activation energy of RDX decrease by 68.6 kJ mol−1.

Heteroatoms in situ-doped hierarchical porous hollow-activated carbons (HPHACs) have been prepared innovatively by pyrolyzation of setaria viridis combined with alkaline activation for the first time. The micro-morphology, pore structure, chemical compositions, and electrochemical properties are researched in detail. The obtained HPHACs are served as outstanding electrode materials in electrochemical energy storage ascribe to the particular hierarchical porous and hollow structure, and the precursor setaria viridis is advantage of eco-friendly as well as cost-effective. Electrochemical measurement results of the HPHACs electrodes exhibit not only high specific capacitance of 350 F g−1 at 0.2 A g−1, and impressive surface specific capacitance (Cs) of 49.9 μF cm−2, but also substantial rate capability of 68% retention (238 F g−1 at 10 A g−1) and good cycle stability with 99% retention over 5000 cycles at 5 A g−1 in 6 M KOH. Besides, the symmetrical supercapacitor device based on the HPHACs electrodes exhibits excellent energy density of 49.5 Wh kg−1 at power density of 175 W kg−1, but still maintains favorable energy density of 32.0 Wh kg−1 at current density of 1 A g−1 in 1-ethy-3-methylimidazolium tetrafluoroborate ( EMIMBF4) ionic liquid electrolyte, and the excellent cycle stability behaviour shows the nearly 97% ratio capacitance retention of the initial capacitance after 10,000 cycles at current density of 2 A g−1. Overall, the results indicate that HPHACs derived from setaria viridis have appealing electrochemical performances thus are promising electrode materials for supercapacitor devices and large-scale applications.

A novel approach was presented for deposition of nickel–graphene nanocomposite coating on copper. Unlike conventional methods, graphene and graphene oxide nanosheets were not used. The basis of the method is to synthesize graphene oxide by oxidation of graphite anode during the electrochemical deposition process. The obtained graphene oxide sheets were reduced during the deposition in the cathode and co-formed with the nickel deposition in the coating. The pulsed ultrasonic force was applied during the deposition process. When the ultrasonic force stops, the deposition process begins. Scanning electron microscopy, Raman spectroscopy, atomic force microscopy, X-ray diffraction and X-ray photoelectron spectroscopy confirmed the presence of graphene nanosheets in the coating. The amount of graphene nanosheets increases up to a maximum of 14.8 wt% by increasing the time of applying ultrasonic force to 6 s. In addition, with the presence of graphene in the nickel coating, the wear rate dramatically decreased.