17 research outputs found

    A Clean and General Strategy To Decorate a Titanium Metal–Organic Framework with Noble-Metal Nanoparticles for Versatile Photocatalytic Applications

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    We demonstrate a facile and general approach for the fabrication of highly dispersed Au, Pd, and Pt nanoparticles (NPs) on MIL-125­(Ti) without using extra reducing and capping agents. Noble-metal NP formation is directed by an in situ redox reaction between the reductive MIL-125­(Ti) with Ti<sup>3+</sup> and oxidative metal salt precursors. The resulting composites function as efficient photocatalysts

    Preparation of MIL-53(Fe)-Reduced Graphene Oxide Nanocomposites by a Simple Self-Assembly Strategy for Increasing Interfacial Contact: Efficient Visible-Light Photocatalysts

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    In this work, MIL-53­(Fe)-reduced graphene oxide (M53-RGO) nanocomposites have been successfully fabricated by a facile and efficient electrostatic self-assembly strategy for improving the interfacial contact between RGO and the MIL-53­(Fe). Compared with D-M53-RGO (direct synthesis of MIL-53­(Fe)-reduced graphene oxide nanocomposites via one-pot solvothermal approach), M53-RGO nanocomposites exhibit improved photocatalytic activity compared with the D-M53-RGO under identical experimental conditions. After 80 min of visible light illumination (λ ≥ 420 nm), the reduction ratio of Cr­(VI) is rapidly increased to 100%, which is also higher than that of reference sample (N-doped TiO<sub>2</sub>). More significantly, the M53-RGO nanocomposites are proven to perform as bifunctional photocatalysts with considerable activity in the mixed systems (Cr­(VI)/dyes) under visible light, which made it a potential candidate for industrial wastewater treatment. Combining with photoelectrochemical analyses, it could be revealed that the introduction of RGO would minimize the recombination of photogenerated electron–hole pairs. Additionally, the effective interfacial contact between MIL-53­(Fe) and RGO surface would further accelerate the transfer of photogenerated electrons, leading to the enhancement of photocatalytic activity of M53-RGO toward photocatalytic reactions. Finally, a possible photocatalytic reaction mechanism is also investigated in detail

    One-Dimensional CdS/TiO<sub>2</sub> Nanofiber Composites as Efficient Visible-Light-Driven Photocatalysts for Selective Organic Transformation: Synthesis, Characterization, and Performance

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    CdS/TiO<sub>2</sub> heterojunction nanofibers have been successfully synthesized through the photodeposition of CdS on 1D TiO<sub>2</sub> nanofibers that were prepared via a facile electrospinning method. The as-synthesized samples showed high photocatalytic activities upon selectively oxidizing a series of alcohols into corresponding aldehydes under visible light irradiation. TEM observations revealed that CdS was closely grown on the TiO<sub>2</sub> nanofibers. Moreover, it was found that the CdS/TiO<sub>2</sub> nanofibers that were photodeposited for 4 h exhibited the highest catalytic activity, with a conversion of 22% and a selectivity of 99%, which were much higher than those of commercial CdS. In addition, we also discuss the photoabsorption performance and the reaction mechanism of the photocatalytic oxidation of alcohols

    Summary of MRI imaging data of involved joints in ERA patients at disease onset.

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    <p><sup>†</sup>frequency/total, n (%), between-group comparisons: chi-square test.</p><p>*p<0.05 denotes a significant difference between different groups.</p><p>Summary of MRI imaging data of involved joints in ERA patients at disease onset.</p

    Drug treatment in ERA at onset, 6 months, 12 months, 18 months and end of follow-up.

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    <p>Biologic agents were etanercept and adalimumab.</p><p>NSAID, non-steroidal anti-inflammatory drug; DMARD, disease-modifying anti-rheumatic drug.</p><p><sup>†</sup>frequency/total, n (%), between-group comparisons: chi-square test.</p><p><sup>§</sup> frequency/total, n (%), between-group comparisons: continuity correction.</p><p>*p<0.05 denotes a significant difference between different groups.</p><p>Drug treatment in ERA at onset, 6 months, 12 months, 18 months and end of follow-up.</p

    MRI findings of frequently involved joints.

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    <p>(a, b, c and d) Bone marrow edema (BME) appears as hyperintense signal in SPAIR sequence, reflecting active inflammatory lesion. a SPAIR image of wrist demonstrates BME on the carpal. b SPAIR image of a ankle shows BME at the tibiofibula. c SPAIR image of sacroiliac joint shows BME on the left of sacroiliac joint. d SPAIR image of a knee joint shows BME at the distal femur.</p

    Clinical distribution of articular involvement at ERA onset.

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    <p><sup>†</sup>frequency/total, n (%), between-group comparisons: chi-square test.</p><p>*p<0.05 denotes a significant difference between different groups.</p><p>Clinical distribution of articular involvement at ERA onset.</p

    US abnormalitis in entheses.

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    <p>a shows tendon sheath with fluid, vacularization and synovial proliferation. b shows marked calcific insertional tendinopathy. c shows the signal of power doppler which is located inside the calcaneal tendon and tendon thickening. d demonstrates anterior tibial tendon with hypoechogenicity. e and f show the Achilles tendon of the same patient. e demostrates the normal Achilles tendon. f shows tendon thickening and calcaneal erosions.</p

    Clinical features of ERA patients at the end of two-year follow-up.

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    <p>CHAQ, Childhood Health Assessment Questionnaire.</p><p><sup>†</sup>frequency/total, n (%), between-group comparisons: chi-square test.</p><p><sup>‡</sup>mean (standard deviation), between-group comparison: Student’s t-test.</p><p>*p<0.05 denotes a significant difference between different groups.</p><p>Clinical features of ERA patients at the end of two-year follow-up.</p

    Clinical distribution of enthesitis examined at disease onset.

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    <p><sup>†</sup>frequency/total, n (%), between-group comparisons: chi-square test.</p><p>*p<0.05 denotes a significant difference between different groups.</p><p>Clinical distribution of enthesitis examined at disease onset.</p
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