973 research outputs found

    Long-Term Deflection Prediction from Computer Vision-Measured Data History for High-Speed Railway Bridges

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    Management of the vertical long-term deflection of a high-speed railway bridge is a crucial factor to guarantee traffic safety and passenger comfort. Therefore, there have been efforts to predict the vertical deflection of a railway bridge based on physics-based models representing various influential factors to vertical deflection such as concrete creep and shrinkage. However, it is not an easy task because the vertical deflection of a railway bridge generally involves several sources of uncertainty. This paper proposes a probabilistic method that employs a Gaussian process to construct a model to predict the vertical deflection of a railway bridge based on actual vision-based measurement and temperature. To deal with the sources of uncertainty which may cause prediction errors, a Gaussian process is modeled with multiple kernels and hyperparameters. Once the hyperparameters are identified through the Gaussian process regression using training data, the proposed method provides a 95% prediction interval as well as a predictive mean about the vertical deflection of the bridge. The proposed method is applied to an arch bridge under operation for high-speed trains in South Korea. The analysis results obtained from the proposed method show good agreement with the actual measurement data on the vertical deflection of the example bridge, and the prediction results can be utilized for decision-making on railway bridge maintenance

    Bayesian Prediction of Pre-Stressed Concrete Bridge Deflection Using Finite Element Analysis

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    Vertical deflection has been emphasized as an important safety indicator in the management of railway bridges. Therefore, various standards and studies have suggested physics-based models for predicting the time-dependent deflection of railway bridges. However, these approaches may be limited by model errors caused by uncertainties in various factors, such as material properties, creep coefficient, and temperature. This study proposes a new Bayesian method that employs both a finite element model and actual measurement data. To overcome the limitations of an imperfect finite element model and a shortage of data, Gaussian process regression is introduced and modified to consider both, the finite element analysis results and actual measurement data. In addition, the probabilistic prediction model can be updated whenever additional measurement data is available. In this manner, a probabilistic prediction model, that is customized to a target bridge, can be obtained. The proposed method is applied to a pre-stressed concrete railway bridge in the construction stage in the Republic of Korea, as an example of a bridge for which accurate time-dependent deflection is difficult to predict, and measurement data are insufficient. Probabilistic prediction models are successfully derived by applying the proposed method, and the corresponding prediction results agree with the actual measurements, even though the bridge experienced large downward deflections during the construction stage. In addition, the practical uses of the prediction models are discussed

    Ultrafast Intramolecular Proton Transfer Reaction of 1,2- Dihydroxyanthraquinone in the Excited State

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    1,2-Dihydroxyanthraquinone (alizarin) shows an ultrafast intramolecular proton transfer in the excited states between the adjacent hydroxyl and carbonyl groups. Due to the ground and electronic structure of locally excited and proton-transferred tautomers, alizarin shows dual emission bands with strong Stokes shifts. The energy barriers between the locally excited (LE) and proton-transferred (PT) tautomers in the excited state are strongly dependent on the solvent polarity and thus alizarin shows complicated photophysical properties including solvent and excitation dependences. The excited-state intramolecular proton transfer (ESIPT) of alizarin was monitored in time-resolved stimulated Raman spectroscopic investigation, where the instantaneous structural changes of anthraquinone backbone in 70~80 fs were captured. Two major vibrational modes of alizarin, ν(C=C) and ν(C=O) represent the proton transfer reaction in the excited state, which then leads to the vibrational relaxation of the product and the restructuring of solvent molecules. Ultrafast changes in solvent vibrational modes of dimethyl sulfoxide (DMSO) were also investigated for the solvation dynamics including hydrogen bond breaking and reformation

    Molecular Recognition of Arginine by Supramolecular Complexation with Calixarene Crown Ether Based on Surface Plasmon Resonance

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    Arginine plays an important role in cell division and the functioning of the immune system. We describe a novel method by which arginine can be identified using an artificial monolayer based on surface plasmon resonance (SPR). The affinity of arginine binding its recognition molecular was compared to that of lysine. In fabrication of an arginine sensing interface, a calix[4]crown ether monolayer was anchored onto a gold surface and then characterized by Fourier Transform infrared reflection absorption spectroscopy, atomic force microscopy, and cyclic voltammetry. The interaction between arginine and its host compound was investigated by SPR. The calix[4]crown ether was found to assemble as a monolayer on the gold surface. Recognition of calix[4]crown monolayer was assessed by the selective binding of arginine. Modification of the SPR chip with the calix[4]crown monolayer provides a reliable and simple experimental platform for investigation of arginine under aqueous conditions

    Self‐Assembly Mechanism of Spiky Magnetoplasmonic Supraparticles

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/106774/1/adfm201302405.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/106774/2/adfm201302405-sup-0001-S1.pd

    Subtle cytotoxicity and genotoxicity differences in superparamagnetic iron oxide nanoparticles coated with various functional groups

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    Superparamagnetic iron oxide nanoparticles (SPIONs) have been widely utilized for the diagnosis and therapy of specific diseases, as magnetic resonance imaging (MRI) contrast agents and drug-delivery carriers, due to their easy transportation to targeted areas by an external magnetic field. For such biomedical applications, SPIONs must have multifunctional characteristics, including optimized size and modified surface. However, the biofunctionality and biocompatibility of SPIONs with various surface functional groups of different sizes have yet to be elucidated clearly. Therefore, it is important to carefully monitor the cytotoxicity and genotoxicity of SPIONs that are surfaced-modified with various functional groups of different sizes. In this study, we evaluated SPIONs with diameters of approximately 10 nm and 100~150 nm, containing different surface functional groups. SPIONs were covered with −O− groups, so-called bare SPIONs. Following this, they were modified with three different functional groups – hydroxyl (−OH), carboxylic (−COOH), and amine (−NH2) groups – by coating their surfaces with tetraethyl orthosilicate (TEOS), (3-aminopropyl)trimethoxysilane (APTMS), TEOS-APTMS, or citrate, which imparted different surface charges and sizes to the particles. The effects of SPIONs coated with these functional groups on mitochondrial activity, intracellular accumulation of reactive oxygen species, membrane integrity, and DNA stability in L-929 fibroblasts were determined by water-soluble tetrazolium, 2′,7′-dichlorodihydrofluorescein, lactate dehydrogenase, and comet assays, respectively. Our toxicological observations suggest that the functional groups and sizes of SPIONs are critical determinants of cellular responses, degrees of cytotoxicity and genotoxicity, and potential mechanisms of toxicity. Nanoparticles with various surface modifications and of different sizes induced slight, but possibly meaningful, changes in cell cytotoxicity and genotoxicity, which would be significantly valuable in further studies of bioconjugation and cell interaction for drug delivery, cell culture, and cancer-targeting applications

    3D hierarchically porous magnetic molybdenum trioxide@gold nanospheres as a nanogap-enhanced Raman scattering biosensor for SARS-CoV-2

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    A multifunctional 3D magnetic molybdenum trioxide@gold nanosphere is deployed as a plug and play biosensor for SARS-CoV-2 spike proteins via ACE2-mediated immunocapture and magnetic-induced nanogap-enhanced Raman scattering (MINERS)

    Theory of plasmon-enhanced Foerster energy transfer in optically-excited semiconductor and metal nanoparticles

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    We describe the process of Foerster transfer between semiconductor nanoparticles in the presence of a metal subsystem (metal nanocrystals). In the presence of metal nanocrystals, the Foerster process can become faster and more long-range. The enhancement of Foerster transfer occurs due to the effect of plasmon-assisted amplification of electric fields inside the nanoscale assembly. Simultaneously, metal nanocrystals lead to an increase of energy losses during the Foerster transfer process. We derive convenient equations for the energy transfer rates, photoluminescence intensities, and energy dissipation rates in the please of plasmon resonances. Because of strong dissipation due to the metal, an experimental observation of plasmon-enhanced Foerster transfer requires special conditions. As possible experimental methods, we consider cw- and time-resolved photoluminescence studies and describe the conditions to observe plasmon-enhanced transfer. In particular, we show that the photoluminescence spectra should be carefully analyzed since the plasmon-enhanced Foerster effect can appear together with strong exciton energy dissipation. Our results can be applied to a variety of experimental nanoscale systems.Comment: 60 page

    Flood fragility analysis for bridges with multiple failure modes

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    Bridges are one of the most important infrastructure systems that provide public and economic bases for humankind. It is also widely known that bridges are exposed to a variety of flood-related risk factors such as bridge scour, structural deterioration, and debris accumulation, which can cause structural damage and even failure of bridges through a variety of failure modes. However, flood fragility has not received as much attention as seismic fragility despite the significant amount of damage and costs resulting from flood hazards. There have been few research efforts to estimate the flood fragility of bridges considering various flood-related factors and the corresponding failure modes. Therefore, this study proposes a new approach for bridge flood fragility analysis. To obtain accurate flood fragility estimates, reliability analysis is performed in conjunction with finite element analysis, which can sophisticatedly simulate the structural response of a bridge under a flood by accounting for flood-related risk factors. The proposed approach is applied to a numerical example of an actual bridge in Korea. Flood fragility curves accounting for multiple failure modes, including lack of pier ductility or pile ductility, pier rebar rupture, pile rupture, and deck loss, are derived and presented in this study.ope

    Small molecule-induced simultaneous destabilization of β-catenin and RAS is an effective molecular strategy to suppress stemness of colorectal cancer cells

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    Background Cancer stem cells (CSCs), the major driver of tumorigenesis, is a sub-population of tumor cells responsible for poor clinical outcomes. However, molecular mechanism to identify targets for controlling CSCs is poorly understood. Methods Gene Set Enrichment Analyses (GSEA) of Wnt/β-catenin and RAS signaling pathways in stem-like subtype of colorectal cancer (CRC) patients were performed using two gene expression data set. The therapeutic effects of destabilization of β-catenin and RAS were tested by treatment of small molecule KYA1797K using CRC patient derived cells. Results Treatment with KYA1797K, a small molecule that destabilizes both β-catenin and RAS via Axin binding, effectively suppresses the stemness of CSCs as shown in CRC spheroids and small intestinal tumors of ApcMin/+/K-RasG12DLA2 mice. Moreover, KYA1797K also suppresses the stemness of cells in CRC patient avatar model systems, such as patient-derived tumor organoids (PDTOs) and patient-derived tumor xenograft (PDTX). Conclusion Our results suggest that destabilization of both β-catenin and RAS is a potential therapeutic strategy for controlling stemness of CRC cells.This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean Government (MSIP) (grants 2016R1A5A1004694, 2019R1A2C3002751, 2018R1D1A1B07050189)
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