In July, Forbes announced its “America’s Richest Self-Made Women” list for 2018 and Rhode Island’s Carolyn Rafaelian came in at #21 on the list.

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Now, with these facts, it is incumbent on every patriotic leadership to further the debate as well as interrogate how well the youths in the diaspora could contribute to the sustainability of democracy while simultaneously advancing the cause of economic growth and prosperity.

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Mr Hammond’s gloomy warnings about Brexit have also infuriated Tory Eurosceptics, leading to fears in Downing Street that some MPs could try to pick holes in the Budget to undermine his position.

We must also admit that it is a nation that has provided the best of the basics for its citizens and care particularly for the youths, either at home or abroad, has the right to make the sort of demand Kennedy made. The future of any country belongs to the development of youth through enabling program. PERIOD!

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The paper appears in the journal Applied Catalysis B: Environmental. Additional authors are from South China Agricultural University.

MGT nanocomposites were prepared through a layer-by-layer coating process (23). Magnetic Fe3O4 NPs were prepared through modified solvothermal reaction by reduction of FeCl3 (23). As shown in transmission electron microscopy (TEM) images (fig. S1A), the as-prepared Fe3O4 NPs were highly uniform with diameters of 120 ± 5 nm. We observed a well-resolved lattice fringe with an interplanar distance of 0.26 nm for Fe3O4, which corresponds to the (311) plane of magnetite (fig. S1B). In addition, hysteresis loops of Fe3O4 particles in fig. S1C indicate high-performance magnetic properties without remanence or coercivity at 300 K. We coated Fe3O4 NPs with GO through electrostatic adsorption with the linkage of polydimethyldiallylammonium chloride (PDDA) to produce magnetic Fe3O4@GO (MG). Scanning electron (SEM) micrographs (Fig. 2A) show that Fe3O4 NPs were effectively coated with GO. TEM images show that the irregular shapes of the nanocomposites were highly dispersed with diameters of 150 to 250 nm (Fig. 2B). Then, we prepared the uniform porous TiO2 shell via a versatile kinetics-controlled coating method to produce MGT nanocomposites. We observed the ternary heterostructure of MGT (size, 200 to 400 nm) coated by the aggregated TiO2 NPs (~8 nm) and with uniform pores (~5 nm; Fig. 2, C and D). N2 sorption isotherms (Fig. 2E) of the nanocomposites after calcination show typical type IV curves with distinct hysteresis loops close to the H1 type. The Brunauer-Emmett-Teller surface area and the pore volume of the as-prepared nanostructures were calculated to be as high as 105 m2 g−1 and 0.16 cm3 g−1, respectively. The corresponding pore size distribution curves (Fig. 2F) derived from the adsorption branches of the isotherms using the Barrett-Joyner-Halenda method show a sample pore size of ~4.3 nm, which was similar to that obtained from the SEM image. A high-resolution TEM (HR-TEM) image [Fig. 2G (III)] shows that the TiO2 NPs were crystallized with a well-resolved lattice fringe with an interplanar distance of 0.24 nm, which corresponds to the (103) plane of anatase (24). We carried out energy dispersive spectroscopy (EDS) to characterize the elemental composition and the structural relationship of the nanostructures from every step obtained (Fig. 2G). It was clear that Fe was located at the center of nanocomposites, while the shell contained C and Ti, which were well separated from each other. X-ray diffraction (XRD) fitted well to those of Fe3O4, GO, and TiO2 bulk phases (Fig. 2H). The diffraction peaks of Fe3O4 were ascribed to the (220), (311), and (440) planes. After Fe3O4 was coated with GO and TiO2, two additional diffraction peaks were observed at 21.2° and 43.3°, which should be ascribed to GO. Several new diffraction peaks appeared at 25.3°, 37.8°, 38.6°, 48.1°, 53.9°, and 55.1°, assigned to the (101), (004), (112), (200), (105), and (211) planes of anatase-phase TiO2, respectively (25, 26), confirming the successful preparation of MGT. We further used Raman and Fourier transform infrared (FTIR) spectroscopy to characterize the as-prepared MGT. As depicted in Fig. 2I, three distinct peaks at 397, 518, and 640 cm−1 in the Raman spectrum of MGT were observed, indicating the presence of anatase-phase TiO2 (26, 27). In the FTIR spectra of MGT (Fig. 2J), two additional infrared bands assigned to Ti–O–C at 1680 cm−1 and Ti–O–H stretching vibration at 3260 cm−1 were observed (28). Both Raman and FTIR results indicated that the MGT nanocomposites were successfully synthesized. The stepwise assembly of MGT was also monitored by microeletrophoresis measurements whose results were expressed as ζ-potentials (fig. S1D). Because of the superparamagnetic properties of the magnetic cores of MGT (Fig. 2K), the MGT nanocomposites were conveniently separated from the reaction solution after the photodegradation treatment upon application of an extended magnetic field. Moreover, it is known that TiO2 shows absorption ranging from 200 to 350 nm. On the other hand, absorbance of MGT nanocomposites extended to the visible region (400 to 600 nm) because of the conjugation of TiO2 with visible GO (fig. S1E) (26). Figure S2 shows the Raman spectra of copper phthalocyanine (CuPc) before and after illumination under visible light (460 nm < λ < 700 nm, 1000 W) on MGT nanocomposites. The intensity of the Raman spectra of CuPc sharply decreased after illumination by visible light for 90 min, revealing that CuPc was significantly photodegraded (26). In contrast, we obtained negligible changes for MT NPs (fig. S2, B and C). Accordingly, after five cycles of enrichment followed by illumination, the SERS activity of MGT remained more than 98% (fig. S2D), confirming the good recyclability of MGT. Considering the photocatalytic activity of MGT under the visible light region, we investigated the Raman signal reproducibility of MGT in fig. S3. After irradiating 15 times with an exposure time of 1 s, the Raman intensity of CuPc remained approximately 97%, indicating the high stability and reproducibility of MGT substrates. Besides, we measured the surface wettability of MGT through contact angle. As shown in fig. S1F, MGT showed hydrophilic properties with an MGT contact angle of 41° ± 2°, which is suitable for further bio-applications.

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