Publications by authors named "Zishuai Zhang"

Increasing volatile fatty acid (VFA) production via persulfate activation (i.e., chemical effect) in anaerobic digestion (AD) is an emerging resource utilization method.

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Membrane distillation (MD) has great potential in the management of hypersaline water for zero liquid discharge (ZLD) due to its high salinity tolerance. However, the membrane wetting issue significantly restricts its practical application. In this study, a composite membrane tailored for extreme concentrations and even crystallization of hypersaline water is synthesized by coating a commercial hydrophobic porous membrane with a composite film containing a dense polyamide layer, a cation exchange layer (CEL), and an anion exchange layer (AEL).

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Article Synopsis
  • Scientists created a special system using biochar and manganese dioxide to clean dirty water from farms, specifically targeting antibiotic drugs and heavy metals.
  • This system works well at different temperatures, with a 85.5% success rate at room temperature and still performs decently when it's colder.
  • The study shows that this method could help treat wastewater in colder areas better, making it more eco-friendly and useful for farming.
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Article Synopsis
  • * This catalyst achieves a low overpotential of 230 mV for oxygen evolution at 10 mA cm² and maintains stability for over 10 hours without changing its surface structure.
  • * The advancement in this oxygen evolution reaction (OER) catalyst addresses key challenges in hydrogen production technology, potentially lowering costs and enhancing the adoption of electrolyser systems.
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Antibiotic exist in various states after entering agricultural soil through the application of manure, including the aqueous state (I), which can be directly absorbed by plants, and the auxiliary organic extraction state (III), which is closely associated with the pseudo-permanence of antibiotics. However, effective analytical methods for extracting and affecting factors on fractions of different antibiotic states remain unclear. In this study, KCl, acetonitrile/NaEDTA-McIlvaine buffer, and acetonitrile/water were successively used to extract states I, II, and III of 21 antibiotics in soil, and the recovery efficiency met the quantitative requirements.

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Two-dimensional (2D) transition metal borides (MBenes), new members of the 2D materials family, hold great promise for use in the electrocatalytic and energy storage fields because of their high specific area, high chemical activity, and fast charge carrier mobility. Although various types of MBenes are reported, layered MBenes featuring redox-active terminal groups for high energy output are not yet produced. A facile and energy-efficient method for synthesizing MBenes equipped with redox-active terminal groups for cascade Zn||I batteries is presented.

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Plasmids have increasingly become a point of concern since they act as a vital medium for the dissemination of antibiotic resistance genes (ARGs). Although indigenous soil bacteria are critical hosts for these plasmids, the mechanisms driving the transfer of antibiotic resistance plasmids (ARPs) have not been well researched. In this study, we tracked and visualized the colonization of the wild fecal antibiotic resistance plasmid pKANJ7 in indigenous bacteria of different habitat soils (unfertilized soil (UFS), chemical fertilized soil (CFS), and manure fertilized soil (MFS)).

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Here, we detail how the catalytic behavior of immobilized molecular electrocatalysts for the CO reduction reaction (CORR) can be impacted by catalyst aggregation. Raman spectroscopy was used to study the CORR mediated by a layer of cobalt phthalocyanine (CoPc) immobilized on the cathode of an electrochemical flow reactor. We demonstrate that during electrolysis, the oxidation state of CoPc in the catalyst layer is dependent upon the degree of catalyst aggregation.

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Rechargeable aqueous metal||I electrochemical energy storage systems are a cost-effective alternative to conventional transition-metal-based batteries for grid energy storage. However, the growth of unfavorable metallic deposition and the irreversible formation of electrochemically inactive by-products at the negative electrode during cycling hinder their development. To circumvent these drawbacks, herein we propose 3,4,9,10-perylenetetracarboxylic diimide (PTCDI) as negative electrode active material and a saturated mixed KCl/I aqueous electrolyte solution.

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We report here the direct hydrogenation of O gas to form hydrogen peroxide (HO) using a membrane reactor without H gas. Hydrogen is sourced from water, and the reactor is driven by electricity. Hydrogenation chemistry is achieved using a hydrogen-permeable Pd foil that separates an electrolysis chamber that generates reactive H atoms, from a hydrogenation chamber where H atoms react with O to form HO.

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Electrolyzers are now capable of reducing carbon dioxide (CO) into products at high reaction rates but are often characterized by low energy efficiencies and low CO utilization efficiencies. We report here an electrolyzer that reduces 3.0 M KHCO(aq) into CO(g) at a high rate (partial current density for CO of 220 mA cm) and a CO utilization efficiency of 40%, at a voltage of merely 2.

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Article Synopsis
  • - The study focuses on electrochemical reactors that convert carbon monoxide (CO) into valuable chemicals and fuels, highlighting that using concentrated hydroxide electrolyte often leads to unproductive byproducts instead of desired products from CO2 reduction reactions (CO2RR).
  • - It introduces a copper phthalocyanine (CuPc) electrocatalyst, which shows a 25% higher selectivity for acetate formation compared to a well-established oxide-derived copper catalyst, achieving high rates of product formation at current densities over 200 mA/cm.
  • - The research indicates that while CuPc remains structurally unchanged during the reaction, it likely converts to a metallic copper state that still affects its catalytic efficiency, suggesting new methods for producing carbon-neutral
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Here, we quantify the effect of an external magnetic field (β) on the oxygen evolution reaction (OER) for a cobalt oxide|fluorine-doped tin oxide coated glass (CoO|FTO) anode. A bespoke apparatus enables us to precisely determine the relationship between magnetic flux density (β) and OER activity at the surface of a CoO|FTO anode. The apparatus includes a strong NdFeB magnet ( = 450 ± 1 mT) capable of producing a magnetic field of 371 ± 1 mT at the surface of the anode.

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For common hydrogenation chemistries that occur at high temperatures (where H is adsorbed and activated at the same surface which the substrate must also adsorb for reaction), there is often little consensus on how the reactions (e.g., hydro(deoxy)genation) actually occur.

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Thanks to the low cost, free dendritic hazards, and high volumetric capacity, magnesium (Mg)-ion batteries have attracted increasing attention as alternative energy storage devices to lithium-ion batteries. Despite the successful development of electrode materials, the real-life application potential of Mg-ion full battery systems (MIFBSs) is largely hindered by the lack of suitable electrode couples and hence low diffusion kinetics, which induce low specific capacity, poor rate performance, and low working voltage. Herein, we report an aqueous rechargeable MIFBS by employing copper hexacyanoferrate (CuHCF) as the cathode and 3,4,9,10-perylene-tetracarboxylic acid diimide (PTCDI) as the anode in 1 moL L MgCl electrolyte.

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Background: Obtaining comprehensive epidemic information for specific global infectious diseases is crucial to travel health. However, different infectious disease information websites may have different purposes, which may lead to misunderstanding by travelers and travel health staff when making accurate epidemic control and management decisions.

Objective: The objective of this study was to develop a Global Infectious Diseases Epidemic Information Monitoring System (GIDEIMS) in order to provide comprehensive and timely global epidemic information.

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The development of alternatives to vascular bone grafts, the current clinical standard for the surgical repair of large segmental bone defects still today represents an unmet medical need. The subcutaneous formation of transplantable bone has been successfully achieved in scaffolds axially perfused by an arteriovenous loop (AVL) and seeded with bone marrow stromal cells or loaded with inductive proteins. Although demonstrating clinical potential, AVL-based approaches involve complex microsurgical techniques and thus are not in widespread use.

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The local environment and the defect features have made the skull one of the most difficult regions to repair. Finding alternative strategies to repair large cranial defects, thereby avoiding the current limitations of autograft or polymeric and ceramic prostheses constitute an unmet need. In this study, the regeneration of an 8 mm critical-sized calvarial defect treated by autograft or by a monetite scaffold directly placed in the defect or preimplanted (either cranial bone transplant or subcutaneous pocket) and then transplanted within the bone defect is compared.

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