목적 : 본 연구는 Polydimethylsiloxane(PDMS)를 기반으로 다양한 첨가제를 사용하여 고 기능성 안 의료용 고분자를 제조한 후, 제조된 렌즈 표면에 생체적합성 및 습윤성이 우수한 collagen을 코팅하여 물성을 비교 분석 하였다. 방법 : 렌즈 제조를 위해 PDMS와 친수성 모노머인 N,N-dimethylacrylamide(DMA), 2-Hydroxyethyl methacrylate(HEMA)를 주재료로 사용하였으며, 교차결합제인 Ethylene glycol dimethacrylate(EGDMA)와 열 개시제인 Azobisisobutyronitrile(AIBN)을 사용하였다. 또한 기능성 첨가제로는 1,3-Bis(3-aminopropyl) tetramethyldisiloxane(TMDS), Polyvinylpyrrolidone(PVP), 2-(Trifluoromethyl)styrene 및 collagen을 사 용하였다. 제조된 렌즈의 물성 평가를 위해 광투과율, 굴절률, 함수율, 산소투과율 그리고 인장강도를 각각 측정하였으 며, 접촉각 측정을 통해 습윤성을 평가하였다. 결과 : TMDS의 첨가비율에 따라 렌즈의 산소투과율은 약 28~45 ×10⁻¹¹(cm²/sec)(mlO²/ml×mmHg)으로 나타내었으며, PVP 및 2-(Trifluoromethyl)styrene가 첨가된 렌즈의 습윤성 및 인장강도는 56~46° 그리고 0.11~0.17 kgf/mm² 의 범위로 각각 나타났다. 다양한 첨가제를 사용함으로써 제조된 렌즈의 기능성이 향상되었 으며, 특히 콜라겐 첨가제의 사용은 하이드로겔 표면의 접촉각을 매우 감소시켜 우수한 습윤성을 가지는 것으로 나타났다. 결론 : TMDS, PVP 그리고 2-(Trifluoromethyl)styrene은 실리콘 하이드로겔 렌즈의 기능성 향상에 효과적 이며, 첨가제로서의 collagen 사용은 렌즈의 습윤성을 향상시키는 것으로 나타나 본 연구에서 사용된 재료는 안의 료용으로 다양하게 활용될 수 있을 것으로 판단된다.

The current study was intended to synthesize and characterize the physical, chemical, and mechanical properties of carbon/ carbon (C/C) composites using the chemical vapor infiltration (CVI) process. To that end, carbon fiber felt (CF) was used as a preform, and methane and hydrogen were employed as reactive and carrier gases, respectively. After deciding on the optimum temperature (1050 °C), the composite samples were produced at different times (0–195 h). Then the samples were studied for their phase and microstructure characteristics using XRD, SEM, FESEM, FTIR, and Raman spectroscope. The results showed that by increasing the CVI process time up to 195 h, the density of the produced samples increased from 0.20 to 1.62 g/cm3, and the specific surface area decreased from 58.78 to 0.23 m2/ g. Also, by increasing the process duration, the deposition rate decreased due to the reduction of the available surface for carbon deposition. In other words, due to the increase in density, and decrease in both porosity and specific surface area, the thermal conductivity coefficient and the bending strength of the samples increased. The composite specimens’ SEM images of the fracture surface indicated a weak interface between the carbon fibers and the carbon layer developed by the CVI process. The structural analyses showed that the morphology of carbon growth during the CVI process was initially laminar, but changed to rough-laminar (RL) with the higher duration of the CVI process.

Copper nanoparticles (CuNPs) are considered of great importance due to their high catalytic and antimicrobial activities. This study focuses on the preparation and characterization of CuNPs, and on their antibacterial/antifungal activities. A copper salt (copper sulfate pentahydrate) as precursor, starch as stabilizing agent, and ascorbic acid as reducing agent were used to fabricate CuNPs. The resulting product was characterized via different techniques such as X-ray diffractrometry (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and Scanning electron microscopy (SEM) to confirm its characteristic properties. Employing the Scherrer formula, the mean crystallite sizes of copper (Cu) and cuprous oxide (Cu2O) nanocrystals were found to be 29.21 and 25.33 nm, respectively, as measured from the main X-ray diffraction peaks. The functional groups present in the resulting CuNPs were confirmed by FTIR. In addition, the engineered CuNPs showed antibacterial and antifungal activity against tested pathogenic bacterial and fungal strains.

The remarkable electrical, thermal, mechanical, and optical properties of graphene and its derivative grapheme oxide have recently gained great importance, along with the large surface area and single-atoms thickness. In this respect, several techniques of synthesis such as chemical exfoliation, mechanical exfoliation, or chemical synthesis have been discovered. However, the development of graphene with fewer defects and on a large scale poses major challenges; therefore, it is increasingly necessary to produce it in large proportions with high quality. This paper reviews the top-down synthesis approach of graphene and its well-known derivative graphene oxide. Furthermore, characterization of graphene oxide nanomaterial is a critical component of the analysis. The characterization techniques employed to determine the quality, defects intensity, number of layers, and structures for graphene oxide nanomaterial at the atomic scale. This article focuses on the different involved characterization methodology for graphene oxide with their percentage utilization for the past 11 years. Additionally, reviewing all of the characterization literature for the last 11 years would be a difficult task. Therefore, the aim is to outline the existing state of graphene oxide by different characterization techniques and provide a comparative analysis based on their percentage utilization.