Rice husk, in large quantities, is released to the environment due to rice production in Vietnam. If this material can be utilized, it can solve not only the economic issues but also the environmental problems and sustainable development of the country. Laboratory evaluation of asphalt mixture using Nano silica made from rice husk to improve rutting resistance of asphalt mixtures was presented in this study. A 60/70 bitumen was used as control asphalt binder. The ratio of Nano SIO2 used in this study was 0.3%, 0,6%, 0,9%, 1,2%, and 1,5% by weight of powder. A dense gradation with nominal maximum aggregate size of 12.5mm was used for the asphalt mixtures. Marshall stability (MS) test and wheel tracking (WT) test were conducted to evaluate the rutting resistance of asphalt mixtures. It was found that the asphalt mixtures using 0.5%, 1.0%, and 1.5% Nano SIO2 have the rut depths of 5.35mm, 5.39mm, and 5.45mm, respectively, which is 30%, 31% and 29% lower than the control asphalt mixtures at 15,000 load cycles. Moreover, the static modulus of asphalt mixtures using 0.9% Nano SIO2 at 60oC is higher than the control mixtures. Based on the results of this study, it can be concluded that the addition of Nano SIO2 into asphalt mixtures can enhance the rutting performance of asphalt concrete under high temperatures significantly. It is noted that these conclusions were based on only on a limited number of samples and conditions. Further studies must be conducted to investigate the effect of Nano SIO2 on fatigue cracking and moisture damage of asphalt pavement in the field.

5 nm-thick SiO2 layers formed by plasma-enhanced chemical vapor deposition (PECVD) are densified to improve the electrical and interface properties by using nitric acid oxidation of Si (NAOS) method at a low temperature of 121 oC. The physical and electrical properties are clearly investigated according to NAOS times and post-metallization annealing (PMA) at 250 oC for 10 min in 5 vol% hydrogen atmosphere. The leakage current density is significantly decreased about three orders of magnitude from 3.110 × 10−5 A/cm2 after NAOS 5 hours with PMA treatment, although the SiO2 layers are not changed. These dramatically decreases of leakage current density are resulted from improvement of the interface properties. Concentration of suboxide species (Si1+, Si2+ and Si3+) in SiOx transition layers as well as the interface state density (Dit) in SiO2/Si interface region are critically decreased about 1/3 and one order of magnitude, respectively. The decrease in leakage current density is attributed to improvement of interface properties though chemical method of NAOS with PMA treatment which can perform the oxidation and remove the OH species and dangling bond.

본 연구에서는 SiO2 나노파티클-전도성 고분자 PEDOT:PSS 복합 구조 기반의 유기발광다이오 드용 내부 광추출 구조를 간단한 용액 공정으로 제작하였다. 또한, 다양한 농도의 SiO2 나노파티클을 PEDOT:PSS에 분산하여 그 구조를 확인하였고, 상부/하부 버퍼레이어의 도입이 내부 광추출 구조 형성에 미치는 영향에 관하여 알아보았다.

본 연구에서는 PVDF 분리막의 표면의 소수성을 향상시키기 위해 소수성 SiO2 나노 입자를 표면에 고정시키고, 표면에서 나노 입자가 막증류법에 미치는 영향을 확인하고자 한다. 소수성 나노 입자를 부착하는 물리적인 방법으로서 dip-coating 방법을 이용하였다. 나아가 물리적인 방법이 가지는 문제점인 약한 부착력을 해결하기 위해, 표면에 화학적으로 고정시키기 위한 방법으로 PVDF 표면에 OH기를 생성시켜 SiO2 입자의 OH기와의 탈수 반응을 이용하여 고정시켜준다. 이후 SiO2의 소수성 개질을 통해 막 표면의 소수성을 높여 주어 실험을 진행하였다. 앞선 두 가지 부착 방법을 통해 소수성 나노 입자가 PVDF 표면에 부착함에 따른 영향과 부착 방법에 따른 영향을 확인하였다.

A metallic oxide layer of a heat-resistant element contributes to the high-temperature oxidation resistance by delaying the oxidation and has a positive effect on the increase in electrical resistivity. In this study, green compacts of Fecralloy powder mixed with amorphous and crystalline silica are oxidized at 950oC for up to 210 h in order to evaluate the effect of metal oxide on the oxidation and electrical resistivity. The weight change ratio increases as per a parabolic law, and the increase is larger than that observed for Fecralloy owing to the formation of Fe-Si, Fe-Cr composite oxide, and Al2O3 upon the addition of Si oxide. Si oxides promote the formation of Al2O3 and Cr oxide at the grain boundary, and obstruct neck formation and the growth of Fecralloy particles to ensure stable electrical resistivity.

본 연구에서는 고분자 전해질 연료전지(PEFC)의 전해질막의 화학적 안정성의 향상을 위하여 3-mercaptopropyl silica gel (3MPTSG)과 poly(arylene ether sulfone)(SPAES)을 이용하여 복합막을 제조하였다. 일반적으로 방향족 탄화수소계 고분자막은 전극 부분에서 발생한 라디컬에 의한 고분자 산화가 일어나 내구성이 감소하게 되는데 이는 대부분 주쇄에 포함 된 에테르 기 부분의 취약성으로 발생한다. 본 연구에서는 이러한 라디칼에 의한 고분자 주쇄의 산화를 방지하기 위해 친수 성의 무기물 입자를 도입하여 이온전도도 감소율을 최소화하고 산화안정성을 높이고자 하였다. 복합막들의 물성 및 전기화학 적 특성을 평가하기 위해 접촉각, FT-IR, 이온전도도, 이온교환용량(IEC), 함수율, 열안정성 등을 수행하였다. 실리카의 함량 이 0에서 0.5%까지 증가함에 따라 이온전도도 및 함수율은 각각 10% 감소한 0.076 S cm-1 및 16% 감소한 24.6 wt%이었으 나, 산화안정성은 10% 향상되었다.

사용후핵연료 파이로프로세싱에서는 방사성 희토류 염화물(RECl3)을 함유한 LiCl-KCl 공융염폐기물이 발생되며, 핫셀시설에서 운영을 목적으로 단순한 형태의 공융염폐기물 처리공정을 개발하는 것이 필요하다. 본 연구에서는, LiCl-KCl 공융염폐기물 내 희토류 핵종 분리/고화공정의 단순화를 목적으로 Li2O-Al2O3-SiO2-B2O3계의 무기합성매질을 이용하여 LiCl-KCl 공융 염 내 희토류 핵종(Nd)을 분리한 후 분리생성물을 바로 고화하는 시험을 실시하였다. 공융염 내 희토류 염화물(NdCl3) 대비 0.67의 무게비에 해당하는 무기합성매질의 양으로도 Nd 핵종을 98wt% 이상 분리할 수 있었고, 이 때 얻은 희토류 핵종 포집생성물은 약 50wt% 수준의 희토류 산화물 함량을 보유하고 있었으며, 이 포집생성물을 화학적 내구성이 우수한 단일상의 균질한 유리고화체로 제조할 수 있었다. 이 결과들은 LiCl-KCl 공융염폐기물 내 희토류 핵종의 분리/고화공정을 단순화하기 위한 방안수립에 활용될 수 있을 것이다.

Cobalt was electrodeposited onto chemical vapor deposition (CVD) graphene/Si/SiO2 substrates, during different time intervals, using an electrolyte solution containing a low concentration of cobalt sulfate. The intention was to investigate the details of the deposition process (and the dissolution process) and the resulting magnetic properties of the Co deposits on graphene. During and after electrodeposition, in-situ magnetic measurements were performed using an (AGFM). These were followed by ex situ morphological analysis of the samples with ΔtDEP 30 and 100 s by atomic force microscopy in the non-contact mode on pristine CVD graphene/SiO2/Si. We demonstrate that it is possible to electrodeposit Co onto graphene, and that in-situ magnetic measurements can also help in understanding details of the deposition process itself. The results show that the Co deposits are ferromagnetic with decreasing coercivity (HC) and demonstrate increasing magnetization on saturation (MSAT) and electric signal proportional to remanence (Mr), as a function of the amount of the electrodeposited Co. It was also found that, after the end of the dissolution process, a certain amount of cobalt remains on the graphene in oxide form (this was confirmed by X-ray photoelectron spectroscopy), as suggested by the magnetic measurements. This oxide tends to exhibit a limited asymptotic amount when cycling through the deposition/dissolution process for increasing deposition times, possibly indicating that the oxidation process is similar to the graphene surface chemistry.

Transparent organic-inorganic hybrid hard coating films were prepared by the addition of SiO2 or ZrO2, as an inorganic filler to improve the hardness property, filler was highly dispersed in the acrylic resin. To improve the compatibility in the acrylic resin, SiO2 or ZrO2 is surface-modified using various silanes with variation of the modification time and silane content. Depending on the content and kind of the modified inorganic oxide, transparent modified inorganic sols were formulated in acryl resin. Then, the sols were bar coated and cured on PET films to investigate the optical and mechanical properties. The optimized film, which has a modified ZrO2 content of 4 wt% markedly improved in terms of the hardness, haze, and transparency as compared to neat acrylate resin and acrylate resin containing modified SiO2 content of 8 wt%. Meanwhile, the low transparency and high haze of these films slowly appeared at SiO2 content above 10 wt% and ZrO2 content of 5 wt%, but the hardness values were maintained at 2H and 3H, respectively, in comparison with the HB of neat acrylate resin.

Using the ultrasonic pyrolysis method, spherical SiO2 powders were synthesized from aqueous SiO2 sol as a starting material. The effects of pyrolysis conditions such as reaction temperature, SiO2 sol concentration, and physical properties of precursor were investigated for the morphologies of the resulting SiO2 powders. The particle size, shape, and crystallite size of the synthesized SiO2 powders were demonstrated according to the pyrolysis conditions. Generally, the synthesized SiO2 particles were amorphous phase and showed spherical morphology with a smooth surface. It was revealed that increased crystallite size and decreased spherical SiO2 particle size were obtained with increases of the pyrolysis reaction temperature. Also, quantity of spherical SiO2 particles decreased with the decrease in the concentration and surface tension of the precursor.

When a single inorganic precursor is used for the synthesis of a sol-gel coating, there is a problem of cracking on the surface of coating layer. In order to solve this problem of surface cracking, we synthesized inorganic-organic coatings that have hybrid properties of inorganic and organic materials. Sols of various ratios (1:0.07, 0.2, 0.41, 0.82, 1.64, 3.26, 6.54, 13.2) of an inorganic precursor of Tetrabutylorthotitanate (Ti(OBu)4, TBOT) and an organic precursor of γ-Methacryloxy propyltrimethoxysilane (MAPTS) were prepared and coated on stainless steels (SUS316L) by dip coating method. The binding structure and the physical properties of the synthesized coatings were analyzed by FT-IR, FE-SEM, FIB (Focused Ion Beam), and a nano-indenter. Dynamic polarization testing and EIS (electrical impedance spectroscopy) were carried out to evaluate the micro-defects and the corrosion properties of the coatings. The prepared coatings show hybrid properties of inorganic oxides and organic materials. Crack free coatings were prepared when the MAPTS ratio was above a critical value. As the MAPTS ratio increased, the thickness and the corrosion resistance increased, and the hardness decreased.

Zircon, having excellent thermal, chemical, and mechanical properties, is utilized in refractory materials, electronic materials, chemical machines, structural materials, etc. However, zircon generally shows thermal dissociation to zirconia(ZrO2) and silica(SiO2) around the sintering temperature of 1540 oC, and when zircon particles are small and impurities are present, thermal dissociation is known to occur at around 1100 oC. This reduces the mechanical properties of ZrSiO4. In this research, the effect of adding SiO2 and 3Y-TZP to ZrSiO4 has been studied in order to suppress dissociation and improve the mechanical properties. Addition of SiO2 suppressed the dissociation of ZrSiO4 at lower temperatures. It also enabled optimum packing between the particles, resulting in a dense microstructure and good mechanical properties. When 3Y-TZP was added, recombination with the dissociated SiO2 resulted in good mechanical properties by suppressing the generation of pores and the densification of the microstructure.

Poly-methylmetacrylate (PMMA) is mainly applied in the plastic manufacturing industry, but PMMA is weak and gradually got discolor. The strength of PMMA can be improved through organic-inorganic hybrid nano composites with inorganic nano particles such as, SiO2 or ZrO. However, inorganic nano particles are mostly agglomerated spontaneously. In this study, the zeta potential is controlled using different types of organic solvent with different concentrations, dispersibillity of SiO2 nano particles on the PMMA particle are analyzed. When 3 M acetic acid is used, absolute value of the zeta potential is higher, SiO2 nano particle is well attached, and dispersed on the PMMA particle surface. Results indicate that the absolute value of the zeta potential affects the stability of SiO2 dispersion.

Resistance switching memory cells were fabricated using atomically dispersed Pt-SiO2 thin film prepared via RF co-sputtering. The memory cell can switch between a low-resistance-state and a high-resistance-state reversibly and reproducibly through applying alternate voltage polarities. Percolated conducting paths are the origin of the low-resistance-state, while trapping electrons in the negative U-center in the Pt-SiO2 interface cause the high-resistance-state. Intermediate resistance-states are obtained through controlling the compliance current, which can be applied to multi-level operation for high memory density. It is found that the resistance value is related to the capacitance of the memory cell: a 265-fold increase in resistance induces a 2.68-fold increase in capacitance. The exponential growth model of the conducting paths can explain the quantitative relationship of resistance-capacitance. The model states that the conducting path generated in the early stage requires a larger area than that generated in the last stage, which results in a larger decrease in the capacitance.

졸겔법에 의해서 trimethylborate (TMB)/tetraethylorthosilicate (TEOS) 몰비 0.01, 온도 800°C에서 SiO2⋅B2O3가 제조되었다. 그리고 제조된 SiO2⋅B2O3와 PDMS[poly(dimethylsiloxane)]로부터 PDMS-SiO2⋅B2O3 복합막을 제조하고 막의물리화학적 특성을 TG-DTA, FT-IR, BET, X-ray, SEM에 의해 조사하고 그리고 H2와 N2의 투과도와 선택도를 조사하였다.TG-DTA, BET, X-ray, FT-IR 측정에 의하면 SiO2⋅B2O3는 무정형의 다공성 SiO2⋅B2O3였으며, 기공의 평균직경은 37.7821Å, 표면적은 247.6868 m2/g이었다. TGA 측정에 의하면 PDMS 내에 SiO2⋅B2O3가 첨가되었을 때 PDMS-SiO2⋅B2O3 복합막의 열적 안정성은 향상되었다. SEM 관찰에 의하면 SiO2⋅B2O3는 약 1 μm 크기로 PDMS 내에 덩어리 상태로 뭉쳐서 분산되어 있었다. 기체투과실험에 의하면 PDMS 내에 SiO2⋅B2O3 함량이 증가하면 H2와 N2의 투과도는 증가하였고,

(PDDA/SiO2) thin films that consisted of positively charged poly (diallyldimethylammonium chloride) (PDDA) and negatively charged SiO2 nanoparticles were fabricated on a glass substrate by an applying voltage layer-by-layer (LBL) self-assembly method. In this study, the microstructure and optical properties of the (PDDA/SiO2) thin films coated on glass substrate were measured as a function of the applied voltage on the Pt electrodes. When 1.0 V was applied to a Pt electrode in a PDDA and SiO2 solution, the thickness of the (PDDA/SiO2)10 thin film increased from 79 nm to 166 nm. The surface roughness also increased from 15.21 nm to 33.25 nm because the adsorption volume of the oppositely charged PDDA and SiO2 solution increased. Especially, when the voltage was applied to the Pt electrode in the SiO2 solution, the thickness increase of the (PDDA/SiO2) thin film was larger than that obtained when using the PDDA solution. The refractive index of the fabricated (PDDA/SiO2) thin film was ca. n = 1.31~1.32. The transmittance of the glass substrate coated by (PDDA/SiO2)6 thin film with a thickness of 106 nm increased from ca. 91.37 to 95.74% in the visible range.

The effect of titanium dioxide (TiO2) on the properties of color conversion glasses was examined for glasses based on BaO-ZnO-B2O3-SiO2. One glass sample, containing 25 mol% of each component, was used as a reference; the other three glass samples contained 1, 3, and 5 mol% TiO2, respectively. The four color conversion glass samples were prepared by sintering a mixture of glass frits and a YAG:Ce+ phosphor. The characteristics of the color conversion glass samples, such as luminous efficacy, luminance, CIE (Commission International de I'Eclairage) chromaticity, CCT (Correlated Color Temperature), and CRI (Color Rendering Index) were analyzed according to the PL spectrum. The refractive index of the glass samples was found to increase with the titanium dioxide content. In conclusion, luminous efficacy of color conversion glasses increased as the content of TiO2 was raised in the glass matrix.

It is known that bones get damaged by accidents and aging. Since the discovery of Bioglass, various kinds of ceramics have been also found to bond to living bone; some of these ceramics are already being clinically used as bone-repairing materials. In the present study, antibacterial calcium silicate gel (Ag-30CaO·70SiO2 gel) was prepared by sol-gel method in order to control the microstructure, which is related to the dissolution rate and induction period of apatite formation in body environment. In addition, biological Ag-30CaO·70SiO2 is tested. This was done to impart antimicrobial activity to the 30CaO·70SiO2. Ag ion was added during sol-gel synthesis to replace the H2O added during the making of the 30CaO·70SiO2 gel, which has silver solutions of various concentration. After the sol-gel process, 1N-HNO3 solution was used to wash the gel when synthesizing the gel, in order to maintain the porous structure and remove PEG, water soluble polymers. Then, the apatite forming ability of the sol-gel derived CaO-SiO2 gels was investigated using simulated body fluid (SBF), which had almost the same ion concentration as that of human blood plasma. The gels were analyzed by FT-IR spectroscopy, SEM observation, XRD, and fluorescent microscopy. The apatite was successfully created even after washing the gel; apatite is present in an amorphous state, and was found to affect the concentration of the Ag ion in cells in MC3T3 live & dead assay results. From these results, it is suggested that a good material that can be used to repair defects of nature bone is Ag-30CaO·70SiO2 gel.