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Volume Compatibility of Interlayer Treatment Materials with Roller-Compacted Concrete
Xiaoliang Zhu,Yuxin Gao,Wenjing Song,Jingjing Xu,Chengyang Li,Zhaoheng Guo,Fang Chen,Rui Zhang 대한토목학회 2022 KSCE Journal of Civil Engineering Vol.26 No.3
Interlayer is the weakest plane of the entire roller-compacted concrete (RCC) structure and is easily deteriorated under the pressure of water and other environmental factors. Shearing force induced by the different shrinkage in interlayer part is the main reason for that poor performance of the RCC. In this paper, the deformation of RCC concrete and interlayer treatment mortar with supplementary cementitious materials (SCMs, including fly ash and silica fume) and double expansive resources admixtures (HME, containing calcium sulphoaluminate (CSA) and CaO) were studied. Deformation of concrete (produced RCC) and interlayer treatment materials was modeled and compared. Porosity characters of interlayer treatment materials and water absorption of interlayer-treated RCC samples were tested. Results showed that the HME significantly reduced the shrinkage of mortar and the deformation difference degree between layers was shortened. Modified interlayer treatment materials with HME could modify the macroscopic properties of RCC, the low porosity of interlayer and water absorption of interlayer-treated RCC was resulted. The suitable HME content is necessary in interlayer treatment materials and which could improve the performance of RCC.
Localized Surface Plasmon Resonances Caused by Ag Nanoparticles on SiN for Solar Cell Applications
Cheng Yang,Gang Zhang,Hua Min Li,유원종,박영준,김종민 한국물리학회 2010 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.56 No.5
This study examined experimentally and theoretically the coupling of metal (Ag) localized surface plasmon resonances (LSPRs) and a dielectric (SiN) layer to enhance the photovoltaic properties of Si solar cells. The coupling of metal LSPRs and a SiN layer enhanced the intensity and optimized the projection of the internal electromagnetic field induced by the metal LSPRs. Therefore, the overall backscattering and dissipation of light absorption over 400 - 1400 nm were suppressed, resulting in an increase in the photovoltaic conversion efficiency. The mechanism of the coupling of Ag LSPRs and the SiN layer was examined by using a finite element numerical simulation and experiments.
Cheng, Yang,Wang, Yue,Ito, Daisuke,Kong, Deok-Hoon,Ha, Kwon-Soo,Chen, Jun-Hu,Lu, Feng,Li, Jian,Wang, Bo,Takashima, Eizo,Sattabongkot, Jetsumon,Tsuboi, Takafumi,Han, Eun-Taek American Society for Microbiology 2013 Infection and immunity Vol.81 No.5
<P>Merozoite surface protein 1 of <I>Plasmodium vivax</I> (PvMSP1), a glycosylphosphatidylinositol-anchored protein (GPI-AP), is a malaria vaccine candidate for <I>P. vivax</I>. The paralog of PvMSP1, named <I>P. vivax</I> merozoite surface protein 1 paralog (PvMSP1P; PlasmoDB PVX_099975), was recently identified and predicted as a GPI-AP. The similarities in genetic structural characteristics between PvMSP1 and PvMSP1P (e.g., size of open reading frames, two epidermal growth factor-like domains, and GPI anchor motif in the C terminus) led us to study this protein. In the present study, different regions of the PvMSP1P protein, demarcated based on the processed forms of PvMSP1, were expressed successfully as recombinant proteins [i.e., 83 (A, B, and C), 30, 38, 42, 33, and 19 fragments]. We studied the naturally acquired immune response against each fragment of recombinant PvMSP1P and the potential ability of each fragment to bind erythrocytes. The N-terminal fragment (83A) and two C-terminal fragments (33 and 19) reacted strongly with sera from <I>P. vivax</I>-infected patients, with 50 to 68% sensitivity and 95 to 96% specificity, respectively. Due to colocalization of PvMSP1P with PvMSP1, we supposed that PvMSP1P plays a similar role as PvMSP1 during erythrocyte invasion. An <I>in vitro</I> cytoadherence assay showed that PvMSP1P, especially the 19-kDa C-terminal region, could bind to erythrocytes. We also found that human sera from populations naturally exposed to vivax malaria and antisera obtained by immunization using the recombinant molecule PvMSP1P-19 inhibited <I>in vitro</I> binding of human erythrocytes to PvMSP1P-19. These results provide further evidence that the PvMSP1P might be an essential parasite adhesion molecule in the <I>P. vivax</I> merozoite and is a potential vaccine candidate against <I>P. vivax</I>.</P>