본 연구는 스트론튬 이온(Sr²⁺) 처리가 수화 시멘트 복합체의 공극분포 특성에 미치는 영향을 실험적으로 평가하였다. 물- 시멘트비(w/c) 0.3, 0.4, 0.5로 제조된 시멘트 페이스트 시편을 21일간 탈 이온수에서 수중 양생한 후, 각각 두 개의 그룹 으로 나누었다. 첫 번째 그룹은 탈 이온수에서 추가로 7일간 양생하였고, 두 번째 그룹은 30% 질산스트론튬(Sr(NO3)2) 수 용액에서 동일기간 동안 추가 양생하였다. 양생기간 및 조건에 따른 각 시편에 대하여 수은압입법(MIP: Mercury Intrusion Porosimetry)을 사용하여 공극률 및 공극 크기 분포를 분석하였다. 실험 결과, 물-시멘트비가 낮을수록 공극률이 감소하는 것을 확인하였다. 21일과 28일간 탈 이온수에서 양생한 시편 간에는 공극률 차이가 유의미하지 않았으나, 21일 수중양생 후 스트론튬 이온에 7일간 처리된 시편은 공극률이 유의미하게 감소한 것으로 분석되었다. 특히, 물-시멘트비 0.3인 경우 에는 공극률이 33% 이상 감소하는 결과를 보였다. 또한, 공극 크기 분포 특성 분석 결과, 모든 물-시멘트비 조건에서 21 일 양생된 시편에 비해 7일간 추가 양생된 시편은 큰 공극의 양이 줄어들면서 작은 공극의 양이 증가하는 경향을 확인 하였다. 특히, 스트론튬 이온에 처리된 시편의 경우 50nm 이하의 매우 작은 공극의 양이 크게 증가하였다. 이로써 스트 론튬 이온 처리에 의해 수화 시멘트 복합체의 미세조직이 치밀해짐을 확인하였으며, SEM 분석을 통해 이러한 결과를 시 각적으로 확인하였다. 본 연구는 스트론튬 이온을 활용한 시멘트 콘크리트 표면처리 기법이 노후 시멘트 콘크리트 구조 물에 대하여 수분 침투 저항성을 향상시키는 유지관리 기술로서 잠재력을 지니고 있음을 보여준다.

PURPOSES : The effects of strontium cations on the strength of hydrated cement composites as well as the morphology and chemical composition changes of cement hydrates due to strontium treatment are investigated in this study. Subsequently, the potential of a strontiumbased aqueous solution as a near-surface treatment method for hydrated cement composites is evaluated. METHODS : To supply strontium cations to a hydrated cement composite, a 30% strontium nitrate aqueous solution was used. Cement paste (w/c = 0.4) specimens were prepared and cured in the 30% strontium nitrate aqueous solution, which allows the strontium ions to penetrate into the specimen and treat the near-surface region. Compressive and flexural strength tests were performed on both specimens treated by the strontium ions and untreated specimens cured in deionized water, and the test results were compared. To investigate the changes in the morphology and chemical compositions of the cement hydrates due to the treatment, scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS) analyses were performed. RESULTS : The results of the strength tests indicate that both the compressive and flexural strengths of the specimens cured in the 30% strontium nitrate aqueous solution improved significantly compared with the specimens cured in deionized water for the same duration. In particular, the strontium nitrate aqueous solution shows greater improvement in terms of the flexural strength compared with the compressive strength. The maximum penetration depth of strontium into the hydrated cement composite is 5 mm during the first 7 d of immersion and increases to 6.5 mm during the subsequent 14 d. The SEM results show that the microstructure of the hydrated cement composite is densified by the strontium nitrate aqueous solution treatment. The EDS results show that morphology and chemical compositions of the cement hydrates are altered. This implies that the strontium cations can be combined with C–S–H and C–S–A–H phases to form new types of hydrates. CONCLUSIONS : The experimentally results show that the strength of hydrated cement composites can be improved by modifying their near-surface regions via the strontium cation penetration technique. This implies that the strontium-based aqueous solution exhibits high potential for the maintenance and rehabilitation of concrete structures.

Heavy metal pollution has a harmful impact on human health and is regarded as a vital problem. Preparation of a novel, low cost bio-sorbent for heavy metal sorption is the main target of this research. Non-living Chlorella Vulgaris Alga/Date pit activated carbon composite (1:1), (CV/AC), is a novel bio-sorbent prepared by the wet-chemical method for sorption of Pb (II) and Sr (II) from aqueous media. The optimum pH for sorption reaction is 5 and the equilibrium time is achieved within 1 h. The sorption efficiencies are 90.5% for Pb(II) and 95.7% for Sr(II) with initial concentration Co 10 mg L– 1 at 298 K. The monolayer sorption capacities of CV/AC composite at 298 K and pH = 5 were 6.34 ± 0.059, 5.97 ± 0.22 mg g– 1. The saturation capacities were 98.5 and 125 mg g– 1 for Pb (II) and Sr (II), respectively after 10 days. The sorption process is a spontaneous and endothermic reaction. It follows a pseudo-2nd-order mechanism. The results are suggestive of the need to adopt CV/AC composite as a potential bio-sorbent of Pb (II) and Sr (II) for waste water treatment.

Most recently, graphene-related composite-modified electrode surfaces are been widely employed to improve surface interactions and electron transfer kinetics. Hydrothermally prepared strontium pyro niobate (SPN) and reduced graphene oxide/ strontium pyro niobate (RGOSPN) nanostructures reveal excellent morphology. X-ray diffraction analysis of SPN and RGOSPN agree with standard data. Thermogravimetry–differential scanning calorimetry analyses show that RGOSPN has higher thermal stability than SPN. In addition, from the polarization–electric field (P–E) loop measurements, the estimated value of remnant polarization (Pr) and coercive electric field (Ec) of SPN are 0.039 μC cm−2 and − 2.90 kV cm−1 and that of RGOSPN nanocomposite are 0.0139 μC cm−2 and − 2.04 kV cm−1. Cyclic voltammetry measurements show that RGOSPN nanocomposite manifests the possibility of electrochemical reversibility beyond long cycles without change in performance. The redox cycle reveal that RGOSPN can be used as part of a composite electrode for hybrid capacitors dynamic conditions. Moreover, the specific capacitance of SPN and RGOSPN was calculated using galvanostatic charge–discharge (GCD) technique. The observed energy density of 9.1 W h kg−1 in RGOSPN is higher when compared with previous reported values.

Strontium lanthanum vanadate La1-xSrxVO3 (LSVO) is a promising anode material for electrochemical devices, especially for solid oxide fuel cells, thanks to its irregular electrical conductivity. However, the known synthesis methods are incapable of producing well-dispersed LSVO nanoparticles (NPs) with homogeneous size distribution, which partly impedes the applicability of the material. Thus, a new approach to synthesize LSVO NPs with such characteristics is of paramount importance. In the present work, we successfully prepare LSVO NPs with a high dispersion degree and homogeneous size distribution via a modified co-precipitation pathway, followed by hydrogen reduction at a temperature as low as 700 oC. The prepared LSVO NPs display uniform sizes in the range of 50 ~ 100 nm and do not contain any secondary phases, according to XRD analysis. The chemical mechanism of reactions that occur to form the LSVO is thoroughly highlighted. The work functions of NPs measured by the UPS analysis are in the 2.13 ~ 3.62 eV range, making the LSVO powders promising for use in thermionic devices. An explanation of the role of Sr substitution in work function values of LSVO is also proposed.

Homogeneous liquid crystal (LC) alignment on hafnium strontium oxide (HfSrO) films prepared by sol-gel process via ion-beam (IB) bombardment was investigated. Uniform LC alignment was achieved on the IB-irradiated HfSrO films at IB intensity of 1.8 keV. We confirmed the effect of surface morphology on LC alignment using field-emission scanning electron microscope (FE-SEM). In addition, we observed electro-optical characteristics of the twisted-nematic (TN)-LC cells based on HfSrO films to verify the possibility of LC display (LCD) application.

전 세계적으로 원자력 발전소는 442기가 가동 중이며, 62기가 충원될 예정이다. 원자력 발전소의 증가에 따라 방사성 폐기물 유출에 대한 위험성도 증가하였다. 이러한 이유 때문 에, 방사성 폐기물의 처리는 인간, 동물, 식물을 포함하는 자 연 생태계를 보전하는 관점에서 중요하다. 또한, 방사성 폐 기물 유출은 그 지역뿐만 아니라 전 세계적으로 심각한 문 제를 야기한다. 본 연구는 입체 배양세포에 방사성 핵종원 소 (세슘, 스트론튬, 코발트)를 처리하였고 이에 대한 영향력 을 확인하였다. 입체 배양 구조체는 아가로오스 하이드로겔 을 이용하여 제작했으며 암세포 및 정상세포 (HeLa, HepG2, COS-7)를 사용하여 입체 배양을 실시 하였다. 입체 형태로 세포를 배양한 후 세슘, 스트론튬, 코발트 농도 변화에 따라 세포 생존능력을 분석하였다. 이때 입체 배양세포에서 생존 능력이 단층 배양세포 보다 최대 42% 우수한 것을 확인하였 다. 입체 배양구조체는 세포가 형태 및 생리학적으로 in vivo 환경인 조직과 비슷하게 배양을 가능하게 하였다. 따라서, 입체 배양구조체는 기존의 단층 배양 한계점인 in vivo 환경 에 적용시킬 수 없다는 한계를 극복하였다. 본 입체 배양 기 술이 중금속 독성평가 및 단시간 내에 다수의 물질 분석을 수행하는 고속 대량 스크리닝 기술에 활용될 것으로 기대한 다.

In this study, we investigated primary biocompatibility and osteogenic gene expression of porous granular BCP bone substitutes with or without strontium (Sr) doping. In vitro biocompatibility was investigated on fibroblasts like L929 cells and osteoblasts like MG-63 cells using a cell viability assay (MTT) and one cell morphological observation by SEM, respectively. MTT results showed a cell viability percent of L929 fibroblasts, which was higher in Sr-BCP granules (98-101%) than in the non-doped granules (92-96%, p< 0.05). Osteoblasts like MG-63 cells were also found to proliferate better on Sr-doped BCP granules (01-111%) than on the non-doped ones (92-99%, p< 0.05) using an MTT assay. As compared with pure BCP granules, SEM images of MG-63 cells grown on sample surfaces confirmed that cellular spreading, adhesion and proliferation were facilitated by Sr doping on BCP. Active filopodial growth of MG-63 cells was also observed on Sr-doped BCP granules. The cells on Sr-doped BCP granules were well attached and spread out. Gene expression of osteonectin, osteopontin and osteoprotegrin were also evaluated using reverse transcriptase polymerase chain reaction (RT-PCR), which showed that the mRNA phenotypes of these genes were well maintained and expressed in Sr-doped BCP granules. These results suggest that Sr doping in a porous BCP granule can potentially enhance the biocompatibility and bone ingrowth capability of BCP biomaterials.

본 연구는 효율적인 돼지 난자의 활성화를 통한 수핵란의 대량 확보를 위하여 ethanol, Ca-ionophore 및 strontium의 최적 농도 및 노출 시간을 규명하기 위하여 실시되었다. Ethanol은 10%에서 10분간 노출시켰을 때 난할율과 배발달 성적이 각각 51.4%와 45%로 다른 처리구에 비하여 유의적으로 높았으며 (P<0.05), Ca-ionophore는 에서 2분간 노출시켰을 때 난할율과 배발달 성적이 유의적으로 높았다. 또한 st

Sr2Ta2O7, a layered perovskite compound, has been reported to possess most excellent photocatalytic properties among the layered perovskite materials. Recently, we have demonstrated that Ba5Ta4O15 that was prepared under a mol ratio of Ba: Ta=1:1 has high photocatalytic performance as well as Sr2Ta2O7. In this study, the photocatalyst samples with a mol ratio of Sr: Ba: Ta = (1-x): x: 1 were prepared. The maximum photocatalytic performance was obtained for x= 0.2, which is three times as high as that of undoped Sr2Ta2O7.