29 research outputs found

    Active Energy Harvesting from Microbial Fuel Cells at the Maximum Power Point without Using Resistors

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    Microbial fuel cell (MFC) technology offers a sustainable approach to harvest electricity from biodegradable materials. Energy production from MFCs has been demonstrated using external resistors or charge pumps, but such methods can only dissipate energy through heat or receive electrons passively from the MFC without any controllability. This study developed a new approach and system that can actively extract energy from MFC reactors at any operating point without using any resistors, especially at the peak power point to maximize energy production. Results show that power harvesting from a recirculating-flow MFC can be well maintained by the maximum power point circuit (MPPC) at its peak power point, while a charge pump was not able to change operating point due to current limitation. Within 18-h test, the energy gained from the MPPC was 76.8 J, 76 times higher than the charge pump (1.0 J) that was commonly used in MFC studies. Both conditions resulted in similar organic removal, but the Coulombic efficiency obtained from the MPPC was 21 times higher than that of the charge pump. Different numbers of capacitors could be used in the MPPC for various energy storage requirements and power supply, and the energy conversion efficiency of the MPPC was further characterized to identify key factors for system improvement. This active energy harvesting approach provides a new perspective for energy harvesting that can maximize MFC energy generation and system controllability

    Additional file 5 of Analysis of differential membrane proteins related to matrix stiffness-mediated metformin resistance in hepatocellular carcinoma cells

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    Additional file 5: Figure S2. Six typical expression patterns reflect the increase degree of membrane proteins. iTRAQ tags 113, 114, 115, 116, 117 and 118 represent NC-L, NC-M, NC-H, Met-L, Met-M and Met-H, respectively

    Selective Catalytic Hydrodechlorination of 1,2-Dichloroethane to Ethylene over Ni–Rh Nanoparticle Catalysts Supported on γ‑Al<sub>2</sub>O<sub>3</sub>

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    Ni catalysts decorated with trace Rh supported on γ-Al2O3 were prepared by the co-impregnation method. To obtain the Ni–Rh nanoparticles with different nanostructures and chemical compositions, bimetallic catalysts with varied Ni/Rh molar ratios were prepared. For comparison, monometallic Ni/γ-Al2O3 and Rh/γ-Al2O3 catalysts were also prepared by the impregnation method. The selective gas phase catalytic hydrodechlorination of 1,2-dichloroethane to ethylene was used to evaluate catalytic performances of the catalysts. The catalysts were characterized by X-ray diffraction, N2 adsorption, X-ray photoelectron spectroscopy, H2 temperature-programmed reduction, transmission electron microscopy–energy-dispersive X-ray, and CO chemisorption. It was found that the introduction of Rh to Ni catalyst facilitated the generation of spillover hydrogen which could enhance the ability of the Ni catalyst for H2 activation. In bimetallic catalysts, there was an intimate interaction between Ni and Rh, and isolated Rh sites were formed due to the dilution effect of Ni. Accordingly, compared with the monometallic Ni catalyst for gas phase catalytic hydrodechlorination of 1,2-dichloroethane, the bimetallic Ni–Rh(800)/γ-Al2O3 catalyst exhibited markedly higher 1,2-dichloroethane conversion (37%) and comparable selectivity to ethylene (95%). The findings in this study indicate that Ni–Rh/γ-Al2O3 with trace Rh can be used as a promising catalyst for highly effective and selective catalytic hydrodechlorination of chlorinated hydrocarbons

    Additional file 6 of Analysis of differential membrane proteins related to matrix stiffness-mediated metformin resistance in hepatocellular carcinoma cells

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    Additional file 6: Figure S3. Six typical expression patterns reflect the decrease degree of membrane proteins. iTRAQ tags 113, 114, 115, 116, 117 and 118 represent NC-L, NC-M, NC-H, Met-L, Met-M and Met-H, respectively

    Additional file 2 of Analysis of differential membrane proteins related to matrix stiffness-mediated metformin resistance in hepatocellular carcinoma cells

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    Additional file 2: Figure S1. Efficiency and quality identification of membrane protein extraction. (A) The approximate location and range of membrane protein molecules performed by polyacrylamide gel electrophoresis with Coomassie brilliant blue staining. (B)(i, ii) Western blot were performed on the six groups of membrane proteins and cytoplasmic proteins

    Exploring China’s Materialization Process with Economic Transition: Analysis of Raw Material Consumption and Its Socioeconomic Drivers

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    China’s rapidly growing economy is accelerating its materialization process and thereby creating serious environmental problems at both local and global levels. Understanding the key drivers behind China’s mass consumption of raw materials is thus crucial for developing sustainable resource management and providing valuable insights into how other emerging economies may be aiming to accomplish a low resource-dependent future. Our results show that China’s raw material consumption (RMC) rose dramatically from 11.9 billion tons in 1997 to 20.4 billion tons in 2007, at an average annual growth rate at 5.5%. In particular, nonferrous metal minerals and iron ores increased at the highest rate, while nonmetallic minerals showed the greatest proportion (over 60%). We find that China’s accelerating materialization process is closely related to its levels of urbanization and industrialization, notably demand for raw materials in the construction, services, and heavy manufacturing sectors. The growing domestic final demand level is the strongest contributor of China’s growth in RMC, whereas changes in final demand composition are the largest contributors to reducing it. However, the expected offsetting effect from changes in production pattern and production-related technology level, which should be the focus of future dematerialization in China, could not be found

    Chip-scale high-performance photonic microwave oscillator

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    Optical frequency division based on bulk or fiber optics provides unprecedented spectral purity for microwave oscillators. To extend the applications of this approach, the big challenges are to develop miniaturized optical frequency division oscillators without trading off phase noise performance. In this paper, we report a chip-scale electro-optical frequency division microwave oscillator with ultra-low phase noise performance. Dual laser sources are co-self-injection-locked to a single silicon nitride spiral resonator to provide a record high-stability, fully on-chip optical reference. An integrated electro-optical frequency comb based on a novel thin-film lithium niobate phase modulator chip is incorporated for the first time to perform optical-to-microwave frequency division. The resulting chip-scale photonic microwave oscillator achieves a phase noise level of -129 dBc/Hz at 10 kHz offset for 37.7 GHz carrier. The results represent a major advance in high performance, integrated photonic microwave oscillators for applications including signal processing, radar, timing, and coherent communications
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