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Adsorption characteristics of ciprofloxacin onto g-MoS2sub><

Zhenyu Yang, Rong Xing, Wenjun Zhou, Lizhong Zhu

《环境科学与工程前沿（英文）》 2020年第14卷第3期 doi: 10.1007/s11783-019-1218-0

摘要： The g-MoS2 coated composites (g-MoS2-BC) were synthesized. The coated g-MoS2 greatly increased the adsorption ability of biochar. The synergistic effect was observed for CIP adsorption on g-MoS2-RC700. The adsorption mechanisms of CIP on g-MoS2-BC were proposed. The g-MoS2 coated biochar (g-MoS2-BC) composites were synthesized by coating original biochar with g-MoS2 nanosheets at 300°C(BC300)/700°C (BC700). The adsorption properties of the g-MoS2-BC composites for ciprofloxacin (CIP) were investigated with an aim to exploit its high efficiency toward soil amendment. The specific surface area and the pore structures of biochar coated g-MoS2 nanosheets were significantly increased. The g-MoS2-BC composites provided more π electrons, which was favorable in enhancing the π-π electron donor-acceptor (EDA) interactions between CIP and biochar. As a result, the g-MoS2-BC composites showed faster adsorption rate and greater adsorption capacity for CIP than the original biochar. The coated g-MoS2 nanosheets contributed more to CIP adsorption on the g-MoS2-BC composites due to their greater CIP adsorption capacity than the original biochar. Moreover, the synergistic effect was observed for CIP adsorption on g-MoS2-BC700, and suppression effect on g-MoS2-BC300. In addition, the adsorption of CIP onto g-MoS2-BC composites also exhibited strong dependence on the solution pH, since it can affect both the adsorbent surface charge and the speciation of contaminants. It was reasonably suggested that the mechanisms of CIP adsorption on g-MoS2-BC composites involved pore-filling effects, π-π EDA interaction, electrostatic interaction, and ion exchange interaction. These results are useful for the modification of biochar in exploiting the novel amendment for contaminated soils.

关键词： Adsorption Ciprofloxacin g-MoS₂ nanosheets Biochar Soil remediation

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Mercury removal from aqueous solution using petal-like MoS2sub> nanosheets

Ragini Pirarath, Palani Shivashanmugam, Asad Syed, Abdallah M. Elgorban, Sambandam Anandan, Muthupandian Ashokkumar

《环境科学与工程前沿（英文）》 2021年第15卷第1期 doi: 10.1007/s11783-020-1307-0

摘要： Abstract • Synthesized few-layered MoS2 nanosheets via surfactant-assisted hydrothermal method. • Synthesized MoS2 nanosheets show petal-like morphology. • Adsorbent showed 93% of mercury removal efficiency. • The adsorption of mercury is attributed to negative zeta potential (-21.8 mV). Recently, different nanomaterial-based adsorbents have received greater attention for the removal of environmental pollutants, specifically heavy metals from aqueous media. In this work, we synthesized few-layered MoS2 nanosheets via a surfactant-assisted hydrothermal method and utilized them as an efficient adsorbent for the removal of mercury from aqueous media. The synthesized MoS2 nanosheets showed petal-like morphology as confirmed by scanning electron microscope and high-resolution transmission electron microscopic analysis. The average thickness of the nanosheets is found to be about 57 nm. Possessing high stability and negative zeta potential makes this material suitable for efficient adsorption of mercury from aqueous media. The adsorption efficiency of the adsorbent was investigated as a function of pH, contact time and adsorbent dose. The kinetics of adsorption and reusability potential of the adsorbent were also performed. A pseudo-second-order kinetics for mercury adsorption was observed. As prepared MoS2 nanosheets showed 93% mercury removal efficiency, whereas regenerated adsorbent showed 91% and 79% removal efficiency in the respective 2nd and 3rd cycles. The adsorption capacity of the adsorbent was found to be 289 mg/g at room temperature.

关键词： Anionic surfactant 2D material MoS₂ nanosheets Mercury removal Adsorption capacity

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growth of a-few-layered MoS on CdS nanorod for high efficient photocatalytic H production

《能源前沿（英文）》 2021年第15卷第3期页码 752-759 doi: 10.1007/s11708-021-0779-3

摘要： An ultrathin MoS₂ was grown on CdS nanorod by a solid state method using sulfur powder as sulfur source for photocatalytic H₂ production. The characterization result reveals that the ultrathin MoS₂ nanosheets loaded on CdS has a good contact state. The photoelectrochemical result shows that MoS₂ not only are beneficial for charge separation, but also works as active sites, thus enhancing photocatalytic activity. Compared with pure CdS, the photocatalytic activity of MoS₂ loaded CdS was significantly improved. The hydrogen evolution rate on m(MoS₂): m(CdS) = 1: 50 (m is mass) reaches 542 μmol/h, which is 6 times of that on pure CdS (92 μmol/h). This work provides a new design for photocatalysts with high photocatalytic activities and provides a deeper understanding of the effect of MoS₂ on enhancing photocatalytic activity.

关键词： photocatalytic H₂ production CdS MoS₂ cocatalyst charge separation

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hydrogen evolution and simultaneous organic pollutant degradation over an urchin-like oxygen-doped MoS

《环境科学与工程前沿（英文）》 2022年第16卷第10期 doi: 10.1007/s11783-022-1566-z

摘要：

● An urchin-like OMS/ZIS composite was fabricated by a facile solvothermal method.

关键词： Dual-functional photocatalysts Oxygen-doped MoS₂/ZnIn₂S₄ H₂ evolution Organic pollutant

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用于环境催化的MoS2sub>/ZIF-8复合材料——太阳能驱动的抗生素降解工程 Article

陈文倩, 李琳悦, 李林, 裘文慧, 唐量, 徐玲, 许科军, 吴明红

《工程（英文）》 2019年第5卷第4期页码 755-767 doi: 10.1016/j.eng.2019.02.003

摘要：然而，目前使用的TiO2sub>基催化剂仅吸收紫外（UV）区域中的小部分太阳光谱，导致效率降低。在本文中，我们提供了一种MoS2sub>/ZIF-8复合光催化剂，它可以使环丙沙星（CIP）和盐酸四环素（TC）的光催化降解率分别达到1T/2H-MoS2sub>的1.21倍和MoS2sub>/ZIF-8纳米复合材料的产氢率是MoS2sub>的1.79倍。这项工作通过优化表面纳米异质结结构的构造，为探索原始和高效的1T/2H-MoS2sub>/MOF基光催化剂提供了新的方向。我们发现复合光催化剂经久耐用，其催化性能在稳定性测试下得以保持。因此，1T/2H-MoS2sub>/MOF基光催化剂具有良好的抗生素降解工程应用前景。

关键词： 1T/2H-MoS2sub> ZIF-8 抗生素降解光催化

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Application of MoS in the space environment: a review

《机械工程前沿（英文）》 2023年第18卷第3期 doi: 10.1007/s11465-023-0755-1

摘要： A considerable portion of space mechanism failures are related to space tribological problems. Cold welding in high vacuum; surface erosion and collision damage caused by various radiations, high temperature oxidation under atomic oxygen (AO) bombardment; and thermal stress caused by temperature alternation all alter the physical, chemical, and friction properties of materials. In particular, the space vibration caused by alternating temperatures and microgravity environments can alter the motion of the contact body, further affecting its friction properties. Improving the friction properties of contact surfaces in the space environment is an important way to extend the service life of spacecraft. Traditional lubricants can no longer meet the lubrication requirements of the space environment. This study describes the characteristics of the space environment and the applications of solid lubricants. The friction properties of MoS₂, a solid lubricant widely used in space, are discussed. The synergistic lubrication of MoS₂ with surface textures or metals is presented. Advances in research on the friction properties of collision sliding contacts in the space environment are reviewed. The combination of MoS₂ and soft metals with surface textures is introduced to reduce the effects of vibration environments on the friction properties of moving parts in space mechanisms. Finally, the challenges and future research interests of MoS₂ films in space tribology are presented.

关键词： MoS₂ soft metal space environment surface texture synergistic effect vibration

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Magnetic Co-doped 1D/2D structured -FeO/MoS effectively activated peroxymonosulfate for efficient abatement

《环境科学与工程前沿（英文）》 2023年第18卷第3期 doi: 10.1007/s11783-024-1797-2

摘要：

● Magnetic Co- γ -Fe₂O₃/MoS₂ were prepared via facile hydrothermal methods.

关键词： Magnetic Co-γ-Fe₂O₃/MoS₂ Hydrothermal method Bisphenol A Degradation pathways Toxicity analysis

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Enhancing the photoelectrochemical performance of p-silicon through TiO coating decorated with mesoporous MoS

《能源前沿（英文）》 2021年第15卷第3期页码 772-780 doi: 10.1007/s11708-021-0783-7

摘要： MoS₂ is a promising electrocatalyst for hydrogen evolution reaction and a good candidate for cocatalyst to enhance the photoelectrochemical (PEC) performance of Si-based photoelectrode in aqueous electrolytes. The main challenge lies in the optimization of the microstructure of MoS₂, to improve its catalytic activity and to construct a mechanically and chemically stable cocatalyst/Si photocathode. In this paper, a highly-ordered mesoporous MoS₂ was synthesized and decorated onto a TiO₂ protected p-silicon substrate. An additional TiO₂ necking was introduced to strengthen the bonding between the MoS₂ particles and the TiO₂ layer. This meso-MoS₂/TiO₂/p-Si hybrid photocathode exhibited significantly enhanced PEC performance, where an onset potential of +0.06 V (versus RHE) and a current density of −1.8 mA/cm² at 0 V (versus RHE) with a Faradaic efficiency close to 100% was achieved in 0.5 mol/L H₂SO₄. Additionally, this meso-MoS₂/TiO₂/p-Si photocathode showed an excellent PEC ability and durability in alkaline media. This paper provides a promising strategy to enhance and protect the photocathode through high-performance surface cocatalysts.

关键词： photoelectrocatalysis hydrogen evolution Si photocathode mesoporous MoS₂

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A DNA sensor based on upconversion nanoparticles and two-dimensional dichalcogenide materials

Muskens, Antonios G. Kanaras

《化学科学与工程前沿（英文）》 2021年第15卷第4期页码 935-943 doi: 10.1007/s11705-020-2023-9

摘要： We demonstrate the fabrication of a new DNA sensor that is based on the optical interactions occurring between oligonucleotide-coated NaYF : Yb ; Er upconversion nanoparticles and the two-dimensional dichalcogenide materials, MoS and WS . Monodisperse upconversion nanoparticles were functionalized with single-stranded DNA endowing the nanoparticles with the ability to interact with the surface of the two-dimensional materials via van der Waals interactions leading to subsequent quenching of the upconversion fluorescence. By contrast, in the presence of a complementary oligonucleotide target and the formation of double-stranded DNA, the upconversion nanoparticles could not interact with MoS and WS , thus retaining their inherent fluorescence properties. Utilizing this sensor we were able to detect target oligonucleotides with high sensitivity and specificity whilst reaching a concentration detection limit as low as 5 fmol·L , within minutes.

关键词： upconversion nanoparticles DNA sensor two-dimensional materials MoS₂ WS₂

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NiFeRuOxsub> nanosheets on Ni foam as an electrocatalyst for efficient

《化学科学与工程前沿（英文）》 2023年第17卷第11期页码 1698-1706 doi: 10.1007/s11705-023-2334-8

摘要： The electrocatalyst NiFeRuO_x/NF, comprised of NiFeRuO_x nanosheets grown on Ni foam, was synthesized using a hydrothermal process followed by thermal annealing. NiFeRuO_x/NF displays high electrocatalytic activity and stability for overall alkaline seawater splitting: 98 mV@ 10 mA∙cm⁻² in hydrogen evolution reaction, 318 mV@ 50 mA∙cm⁻² in oxygen evolution reaction, and a cell voltage of 1.53 V@ 10 mA∙cm⁻², as well as 20 h of durability. A solar-driven system containing such a bifunctional NiFeRuO_x/NF has an almost 100% Faradaic efficiency. The NiFeRuO_x coating around Ni foam is an anti-corrosion layer and also a critical factor for enhancement of bifunctional performances.

关键词： NiFeRuO_x nanosheets Ni foam electrocatalysis overall seawater splitting solar-driven system

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基于实时CT扫描技术的CO2sub>和N2sub>交替注入条件下煤吸附膨胀和解吸收缩规律研究 Article

张广磊, P.G. Ranjith, Herbert E. Huppert

《工程（英文）》 2022年第18卷第11期页码 88-95 doi: 10.1016/j.eng.2022.03.010

摘要：

深部煤层是分布最广泛的适宜二氧化碳（CO2sub>）地质封存的地层之一，且通常位于大型CO2sub>排放源附近。将CO2sub>注入到煤层中具有巨大的CO2sub>封存潜力，同时可以提高煤层气的采收率（CO2sub>-ECBM）。本文采用原位同步辐射X射线显微CT扫描技术，首次在原位条件下直接证明了注入氮气（N2sub>）可以置换解吸CO2sub>并减小因CO2sub>吸附引起的煤基质膨胀研究结果表明，煤层中注入经过简单处理的烟道气（主要成分为N2sub>和CO2sub>），是技术上可行的CO2sub>-ECBM 替代方案。其次，N2sub>的存在可以使煤层保持较高的渗透率，实现长期CO2sub>注入封存和煤层气增产。

关键词： CCS CO2sub>-ECBM 碳中和 X 射线成像煤渗透率

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A 3D porous WP2 nanosheets@carbon cloth flexible electrode for efficient electrocatalytic hydrogen evolution

Mingyu Pi, Xiaodeng Wang, Dingke Zhang, Shuxia Wang, Shijian Chen

《化学科学与工程前沿（英文）》 2018年第12卷第3期页码 425-432 doi: 10.1007/s11705-018-1726-7

摘要：

Self-standing porous WP₂ nanosheet arrays on carbon fiber cloth (WP₂ NSs/CC) were synthesized and used as a 3D flexible hydrogen evolution electrode. Because of its 3D porous nanoarray structure, the WP₂ NSs/CC exhibits a remarkable catalytic activity and a high stability. By using the experimental measurements and first-principle calculations, the underlying reasons for the excellent catalytic activity were further explored. Our work makes the present WP₂ NSs as a promising electrocatalyst for hydrogen evolution and provides a way to design and fabricate efficient hydrogen evolution electrodes through 3D porous nano-arrays architecture.

关键词： WP₂ nanosheet arrays hydrogen evolution electrocatalyst flexible electrode

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g-CN-coated MnO hollow nanorod cathode for stable aqueous Zn-ion batteries

《化学科学与工程前沿（英文）》 2023年第17卷第2期页码 217-225 doi: 10.1007/s11705-022-2214-7

摘要： Aqueous zinc-ion batteries are attracting considerable attention because of their high safety compared with conventional lithium-ion batteries. Manganese-based materials have been widely developed for zinc-ion batteries cathode owning to their low cost, high security and simple preparation. However, the severe volume expansion and poor stability during charging and discharging limit the further development of manganese-based cathodes. Herein, superior α-MnO₂@g-C₃N₄ was successfully prepared for stable zinc-ion batteries (ZIBs) cathode by introducing g-C₃N₄ nanosheets. Compared with pure α-MnO₂, α-MnO₂@g-C₃N₄ has a specific capacity of 298 mAh·g^–1 at 0.1 A·g^–1. Even at 1 A·g^–1, the α-MnO₂@g-C₃N₄ still retains 100 mAh·g^–1 (83.4% retention after 5000 cycles), implying its excellent cycling stability. The α-MnO₂@g-C₃N₄-based cathode has the highest energy density (563 Wh·kg^–1) and power energy density (2170 W·kg^–1). This work provides new avenues for the development of a wider range of cathode materials for ZIBs.

关键词： α-MnO₂ hollow nanorods g-C₃N₄ heterojunction aqueous Zn-ion batteries

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Preparation and characterization of hydrothermally engineered TiO

Kanchapogu Suresh, G. Pugazhenthi, R. Uppaluri

《化学科学与工程前沿（英文）》 2017年第11卷第2期页码 266-279 doi: 10.1007/s11705-017-1608-4

摘要： This work targets the preparation and characterization of an inexpensive TiO -fly ash composite membrane for oily wastewater treatment. The composite membrane was fabricated by depositing a hydrophilic TiO layer on a fly ash membrane via the hydrothermal method, and its structural, morphological and mechanical properties were evaluated. The separation potential of the composite membrane was evaluated for 100–200 mg·L synthetic oily wastewater solutions. The results show that the composite membrane has excellent separation performance and can provide permeate stream with oil concentration of only 0.26–5.83 mg·L . Compared with the fly ash membrane in the average permeate flux and performance index (49.97 × 10 m ·m ·s and 0.4620%, respectively), the composite membrane exhibits better performance (51.63 × 10 m ·m ·s and 0.4974%). For the composite ash membrane, the response surface methodology based analysis inferred that the optimum process parameters to achieve maximum membrane flux and rejection are 207 kPa, 200 mg·L and 0.1769 m·s for applied pressure, feed concentration and cross flow velocity, respectively. Under these conditions, predicted responses are 41.33 × 10 m ·m ·s permeate flux and 98.7% rejection, which are in good agreement with the values obtained from experimental investigations (42.84 × 10 m ·m ·s and 98.82%). Therefore, we have demonstrated that the TiO -fly ash composite membrane as value added product is an efficient way to recycle fly ash and thus mitigate environmental hazards associated with the disposal of oily wastewaters.

关键词： TiO₂-fly ash membrane oily wastewater fouling microfiltration

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Rh2sub>O3sub>/hexagonal CePO4sub> nanocatalysts for N2sub>O decomposition

Huan Liu, Zhen Ma

《化学科学与工程前沿（英文）》 2017年第11卷第4期页码 586-593 doi: 10.1007/s11705-017-1659-6

摘要： Hexagonal CePO nanorods were prepared by a precipitation method and hexagonal CePO nanowires were prepared by hydrothermal synthesis at 150 °C. Rh(NO ) was then used as a precursor for the impregnation of Rh O onto these CePO materials. The Rh O supported on the CePO nanowires was much more active for the catalytic decomposition of N O than the Rh O supported on CePO nanorods. The stability of both catalysts as a function of time on stream was studied and the influence of the co-feed (CO , O , H O or O /H O) on the N O decomposition was also investigated. The samples were characterized by N adsorption-desorption, inductively coupled plasma optical emission spectroscopy, X-ray diffraction, transmission electron microscopy, X-ray photoelectron microscopy, hydrogen temperature-programmed reduction, oxygen temperature-programmed desorption, and CO temperature-programmed desorption in order to correlate the physicochemical and catalytic properties.

关键词： Rh₂O₃ CePO₄ N₂O decomposition