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      Synthesis, growth mechanism, optical properties and catalytic activity of ZnO microcrystals obtained via hydrothermal processing

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          Abstract

          Herein we describe ZnO microcrystals obtained viahydrothermal processing at 120, 150 and 180 °C, assisted by CTAB.

          Abstract

          In the present study, typical ZnO microcrystals exhibiting the wurtzite hexagonal crystal structure were produced successfully, characterized by a high degree of crystallinity, viahydrothermal processing at 120, 150 and 180 °C, assisted by N-cetyl- N, N, N-trimethylammonium (CTAB). The samples were characterised by XRD, Raman and infrared, FE-SEM, UV-Vis by diffuse reflectance and photoluminescence (PL). The experimental results confirm that all hydrothermally synthesised ZnO samples were crystallised into a wurtzite hexagonal structure. The ZnO crystals exhibit the morphology of hexagonal columns in the absence and double hexagonal columns in the presence of CTAB. The length and average diameter of the microstructures decrease with increasing processing temperature. It is evident that all the synthesised samples present very similar profiles and band positions in the PL emission spectra, with an emission band in the violet range at approximately 400 nm, a small peak in the UV range at approximately 380 nm, and highly superposed and intense emission bands between 440 and 750 nm (blue to red emission), with a maximum at approximately 610 nm. Furthermore, a nucleation and growth model was proposed to explain the formation of ZnO microcrystals, based on the experimental conditions, that were preferably grown in the [001] direction. In addition, the ZnO exhibited excellent performance in the photocatalytic degradation of rhodamine B (RhB) and methyl orange (MO), achieving 97% and 99% photodegradation of RhB and MO, respectively, when ZnO obtained at 120 °C, in the absence of CTAB, was used as catalyst.

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          Ultrastructural Characterization of the Lower Motor System in a Mouse Model of Krabbe Disease

          Krabbe disease (KD) is a neurodegenerative disorder caused by the lack of β- galactosylceramidase enzymatic activity and by widespread accumulation of the cytotoxic galactosyl-sphingosine in neuronal, myelinating and endothelial cells. Despite the wide use of Twitcher mice as experimental model for KD, the ultrastructure of this model is partial and mainly addressing peripheral nerves. More details are requested to elucidate the basis of the motor defects, which are the first to appear during KD onset. Here we use transmission electron microscopy (TEM) to focus on the alterations produced by KD in the lower motor system at postnatal day 15 (P15), a nearly asymptomatic stage, and in the juvenile P30 mouse. We find mild effects on motorneuron soma, severe ones on sciatic nerves and very severe effects on nerve terminals and neuromuscular junctions at P30, with peripheral damage being already detectable at P15. Finally, we find that the gastrocnemius muscle undergoes atrophy and structural changes that are independent of denervation at P15. Our data further characterize the ultrastructural analysis of the KD mouse model, and support recent theories of a dying-back mechanism for neuronal degeneration, which is independent of demyelination.
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            A review on the visible light active titanium dioxide photocatalysts for environmental applications

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              A comprehensive review of ZnO materials and devices

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2017
                2017
                : 7
                : 39
                : 24263-24281
                Affiliations
                [1 ]Interdisciplinary Laboratory of Advanced Materials
                [2 ]LIMAV
                [3 ]Natural Sciences Centre
                [4 ]CCN
                [5 ]Department of Chemistry
                [6 ]Laboratory of Research in Biology and Chemistry
                [7 ]LPBQ
                [8 ]Campus Coari
                [9 ]Federal Institute of Amazonas
                [10 ]IFAM
                [11 ]GERATEC
                [12 ]Natural Sciences Centre (Centro de Ciências da Natureza)
                [13 ]University of State of Piauí (Universidade Estadual do Piauí)
                [14 ]Teresina
                [15 ]Brazil
                [16 ]Natural and Human Sciences Centre (Centro de Ciências Naturais e Humanas – CCNH)
                [17 ]Federal University of ABC (Universidade Federal do ABC)
                [18 ]09210-170 Santo André
                Article
                10.1039/C7RA03277C
                80955def-b6e6-47d5-9b4e-3638bd71fdcf
                © 2017
                History

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