647 research outputs found
A Taxonomy of Hyperlink Hiding Techniques
Hidden links are designed solely for search engines rather than visitors. To
get high search engine rankings, link hiding techniques are usually used for
the profitability of black industries, such as illicit game servers, false
medical services, illegal gambling, and less attractive high-profit industry,
etc. This paper investigates hyperlink hiding techniques on the Web, and gives
a detailed taxonomy. We believe the taxonomy can help develop appropriate
countermeasures. Study on 5,583,451 Chinese sites' home pages indicate that
link hidden techniques are very prevalent on the Web. We also tried to explore
the attitude of Google towards link hiding spam by analyzing the PageRank
values of relative links. The results show that more should be done to punish
the hidden link spam.Comment: 12 pages, 2 figure
Nuclear superfluidity for antimagnetic rotation in Cd and Cd
The effect of nuclear superfluidity on antimagnetic rotation bands in
Cd and Cd are investigated by the cranked shell model with the
pairing correlations and the blocking effects treated by a particle-number
conserving method. The experimental moments of inertia and the reduced
transition values are excellently reproduced. The nuclear superfluidity is
essential to reproduce the experimental moments of inertia. The two-shears-like
mechanism for the antimagnetic rotation is investigated by examining the shears
angle, i.e., the closing of the two proton hole angular momenta, and its
sensitive dependence on the nuclear superfluidity is revealed.Comment: 14 pages, 4 figure
4-(2,2-Difluoro-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile
In the title compound, C12H6F2N2O2, the 2,2-difluoro-1,3-benzodioxole ring system is approximately planar [maximum deviation = 0.012 (2) Å] and its mean plane is twisted with respect to the pyrrole ring, making a dihedral angle of 2.51 (9)°. In the crystal, N—H⋯N hydrogen bonds link the molecules into chains running along the a axis. π–π stacking is also observed between parallel benzene rings of adjacent molecules, the centroid–centroid distance being 3.7527 (13) Å
Degradation or excretion of quantum dots in mouse embryonic stem cells
<p>Abstract</p> <p>Background</p> <p>Quantum dots (QDs) have been considered as a new and efficient probe for labeling cells non-invasively in vitro and in vivo, but fairly little is known about how QDs are eliminated from cells after labeling. The purpose of this study is to investigate the metabolism of QDs in different type of cells.</p> <p>Results</p> <p>Mouse embryonic stem cells (ESCs) and mouse embryonic fibroblasts (MEFs) were labeled with QD 655. QD-labeling was monitored by fluorescence microscopy and flow cytometry for 72 hours. Both types of cells were labeled efficiently, but a quick loss of QD-labeling in ESCs was observed within 48 hours, which was not prevented by inhibiting cell proliferation. Transmission electron microscope analysis showed a dramatic decrease of QD number in vesicles of ESCs at 24 hours post-labeling, suggesting that QDs might be degraded. In addition, supernatants collected from labeled ESCs in culture were used to label cells again, indicating that some QDs were excreted from cells.</p> <p>Conclusion</p> <p>This is the first study to demonstrate that the metabolism of QDs in different type of cells is different. QDs were quickly degraded or excreted from ESCs after labeling.</p
Cross-linked CoMoO4/rGO nanosheets as oxygen reduction catalyst
Development of inexpensive and robust electrocatalysts towards oxygen reduction reaction
(ORR) is crucial for the cost-affordable manufacturing of metal-air batteries and fuel cells. Here
we show that cross-linked CoMoO4 nanosheets and reduced graphene oxide (CoMoO4/rGO) can
be integrated in a hybrid material under one-pot hydrothermal conditions, yielding a composite
material with promising catalytic activity for oxygen reduction reaction (ORR). Cyclic voltammetry
(CV) and linear sweep voltammetry (LSV) were used to investigate the efficiency of the fabricated
CoMoO4/rGO catalyst towards ORR in alkaline conditions. The CoMoO4/rGO composite revealed
the main reduction peak and onset potential centered at 0.78 and 0.89 V (vs. RHE), respectively.
This study shows that the CoMoO4/rGO composite is a highly promising catalyst for the ORR under
alkaline conditions, and potential noble metal replacement cathode in fuel cells and metal-air batteries
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