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结构功能一体化的高性能陶瓷材料的研究与开发

江东亮

《中国工程科学》 2003年第5卷第2期页码 35-39

摘要：小型化、复合化、低成本制备等要求出发, 并就现有高性能陶瓷材料的基本性能和材料制备工艺上的优缺点进行了分析；简要介绍了碳化硅(SiC)陶瓷、添加Nd的钇铝石榴子石(Nd-YAG)陶瓷、掺有稀土的氮化硅(RE-Si3sub>N4sub>)陶瓷等几种具有结构和功能一体化高性能陶瓷材料的优良性能,可能的应用以及目前存在的问题,特别是在基础研究和制备科学上今后应予以关注的方面。

关键词：结构和功能一体化高性能陶瓷碳化硅 Nd-YAG RE-Si3sub>N4sub>

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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

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Recent advances in special morphologic photocatalysts for NO removal

《环境科学与工程前沿（英文）》 2022年第16卷第11期 doi: 10.1007/s11783-022-1573-0

摘要：

● Systematic information of recent progress in photocatalytic NO_x removal is provided.

关键词： NO_x removal Photocatalyst Graphene C₃N₄ Bi-based compounds.

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acid anions on highly efficient Ce-based catalysts for selective catalytic reduction of NO with NH3sub>

《化学科学与工程前沿（英文）》 2023年第17卷第10期页码 1399-1411 doi: 10.1007/s11705-023-2345-5

摘要： Three kinds of Ce-based catalysts (CePO₄, CeVO₄, Ce₂(SO₄)₃) were synthesized and used for the selective catalytic reduction (SCR) of NO by NH₃. NH₃-SCR performances were conducted in the temperature range of 80 to 400 °C. The catalytic efficiencies of the three catalysts are as follow: CePO₄ > CeVO₄ > Ce₂(SO₄)₃, which is in agreement with their abilities of NH₃ adsorption capacities. The highest NO conversion rate of CePO₄ could reach about 95%, and the catalyst had more than 90% NO conversion rate between 260 and 320 °C. The effect of PO₄^3–, VO₄^3– and SO₄^2– on NH₃-SCR performances of Ce-based catalysts was systematically investigated by the X-ray photoelectron spectroscopy analysis, NH₃ temperature programmed desorption, H₂ temperature programmed reduction and field emission scanning electron microscopy tests. The key factors that can enhance the SCR are the existence of Ce⁴⁺, large NH₃ adsorption capacity, high and early H₂ consumptions, and suitable microstructures for gas adsorption. Finally, CePO₄ and CeVO₄ catalysts also exhibited relatively strong tolerance of SO₂, and the upward trend about 8% was detected due to the sulfation enhancement by SO₂ for Ce₂(SO₄)₃.

关键词： CePO₄ CeVO₄ Ce₂(SO₄)₃ selective catalytic reduction NO removal

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Preparation and lithium storage performances of g-C

Zhengxu BIAN, Zehua TANG, Jinfeng XIE, Junhao ZHANG, Xingmei GUO, Yuanjun LIU, Aihua YUAN, Feng ZHANG, Qinghong KONG

《能源前沿（英文）》 2020年第14卷第4期页码 759-766 doi: 10.1007/s11708-020-0810-0

摘要： As the anode material of lithium-ion battery, silicon-based materials have a high theoretical capacity, but their volume changes greatly in the charging and discharging process. To ameliorate the volume expansion issue of silicon-based anode materials, g-C N /Si nanocomposites are prepared by using the magnesium thermal reduction technique. It is well known that g-C N /Si nanocomposites can not only improve the electronic transmission ability, but also ameliorate the physical properties of the material for adapting the stress and strain caused by the volume expansion of silicon in the lithiation and delithiation process. When g-C N /Si electrode is evaluated, the initial discharge capacity of g-C N /Si nanocomposites is as high as 1033.3 mAh/g at 0.1 A/g, and its reversible capacity is maintained at 548 mAh/g after 400 cycles. Meanwhile, the improved rate capability is achieved with a relatively high reversible specific capacity of 218 mAh/g at 2.0 A/g. The superior lithium storage performances benefit from the unique g-C N /Si nanostructure, which improves electroconductivity, reduces volume expansion, and accelerates lithium-ion transmission compared to pure silicon.

关键词： magnesium thermal reduction g-C₃N₄/Si nanocomposites volume expansion electroconductivity lithium-ion battery

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On the monolayer dispersion behavior of Co3sub>O4sub> on HZSM-5 support: designing applicable

《化学科学与工程前沿（英文）》 2023年第17卷第11期页码 1741-1754 doi: 10.1007/s11705-023-2332-x

摘要： Based on monolayer dispersion theory, Co₃O₄/ZSM-5 catalysts with different loadings have been prepared for selective catalytic reduction of nitrogen oxides by ammonia. Co₃O₄ can spontaneously disperse on HZSM-5 support with a monolayer dispersion threshold of 0.061 mmol 100 m^–2, equaling to a weight percentage around 4.5%. It has been revealed that the quantities of surface active oxygen (O₂^–) and acid sites are crucial for the reaction, which can adsorb and activate NO_x and NH₃ reactants effectively. Below the monolayer dispersion threshold, Co₃O₄ is finely dispersed as sub-monolayers or monolayers and in an amorphous state, which is favorable to generate the two kinds of active sites, hence promoting the performance of ammonia selective catalytic reduction of nitrogen oxide. However, the formation of crystalline Co₃O₄ above the capacity is harmful to the reaction performance. 4% Co₃O₄/ZSM-5, the catalyst close to the monolayer dispersion capacity, possesses the most abundant active O₂^– species and acidic sites, thereby demonstrating the best reaction performance in all the samples. It is proposed the optimal Co₃O₄/ZSM-5 catalyst can be prepared by loading the capacity amount of Co₃O₄ onto HZSM-5 support.

关键词： Co₃O₄/ZSM-5 NO_x-SCR by NH₃ monolayer dispersion threshold effect surface acid sites surface active O₂^– anions

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CH4sub> and N2sub>O emissions from double-rice cropping system as affected by Chinese milk

Heshui XU,Dengyun LI,Bo ZHU,Kai ZHANG,Yadong YANG,Chen WANG,Ying JIANG,Zhaohai ZENG

《农业科学与工程前沿（英文）》 2017年第4卷第1期页码 59-68 doi: 10.15302/J-FASE-2017137

摘要： Chinese milk vetch (CMV) and rice straw (RS) were incorporated into soil to substitute for synthetic N fertilizers and to maintain soil fertility. However, little is known about the integrated impacts of CMV and RS incorporation on CH and N O emissions in double-rice cropping systems in southern China. A field experiment was conducted to estimate the integrated impacts of CMV and RS incorporation in the early- and late-rice seasons on CH and N O emissions. All treatments received uniform N inputs, 6%–37% of which was replaced by CMV and RS crop residue. CMV and/or RS incorporation produced equivalent or slightly more grain yield, while reducing N O emissions by 3%–43%. However, both CMV and RS incorporation increased CH emissions. Annual CH emissions ranged from 321 to 614 kg·hm from CMV and RS amendment treatments, which were 1.5–2.9 times higher than that from synthetic N. Compared with single synthetic N fertilizer, incorporation of CMV and/or RS increased GWP and yield-scaled GWP by 45%–164% and 45%–153%, respectively. Our results demonstrate CMV and RS amendments replacing N fertilizer, maintained stable yield, mitigated N O emission, but enhanced CH emission. Further study is needed on crop residue management in double-cropping rice systems.

关键词： Chinese milk vetch CH₄ double-rice cropping system grain yield N₂O rice straw

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Inexpensive synthesis of a high-performance Fe

Nadir Abbas, Godlisten N. Shao, Syed M. Imran, Muhammad S. Haider, Hee Taik Kim

《化学科学与工程前沿（英文）》 2016年第10卷第3期页码 405-416 doi: 10.1007/s11705-016-1579-x

摘要： A sol-gel technique has been developed for the synthesis of a magnetite-silica-titania (Fe O -SiO -TiO ) tertiary nanocomposite with improved photocatalytic properties based on the use of inexpensive titania and silica precursors. The exceptional photocatalytic activity of the resulting materials was demonstrated by using them to photocatalyze the degradation of methylene blue solution. The best formulation achieved 98% methylene blue degradation. An interesting feature of the present work was the ability to magnetically separate and reuse the catalyst. The efficiency of the catalyst remained high during two reuses. The synthesized nanomaterials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, ultra-violet-visible spectroscopy, diffuse reflectance spectroscopy, and thermogravimetric analysis. XRD analysis revealed the formation of multicrystalline systems of cubic magnetite and anatase titania crystals. SEM and TEM characterization revealed well-developed and homogeneously dispersed particles of size less than 15 nm. FTIR spectra confirmed the chemical interaction of titania and silica. It was further noticed that the optical properties of the prepared materials were dependent on the relative contents of their constituent metal oxides.

关键词： sol-gel photocatalysis magnetic recovery TiO₂ Fe₃O₄ SiO₂

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Chemical deactivation of V

Xiaodong WU, Wenchao YU, Zhichun SI, Duan WENG

《环境科学与工程前沿（英文）》 2013年第7卷第3期页码 420-427 doi: 10.1007/s11783-013-0489-0

摘要： V O -WO /TiO catalyst was poisoned by impregnation with NH Cl, KOH and KCl solution, respectively. The catalysts were characterized by X-ray diffraction (XRD), inductively coupled plasma (ICP), N physisorption, Raman, UV-vis, NH adsorption, temperature-programmed reduction of hydrogen (H -TPR), temperature-programmed oxidation of ammonia (NH -TPO) and selective catalytic reduction of NO with ammonia (NH -SCR). The deactivation effects of poisoning agents follow the sequence of KCl>KOH>>NH Cl. The addition of ammonia chloride enlarges the pore size of the titania support, and promotes the formation of highly dispersed V=O vanadyl which improves the oxidation of ammonia and the high-temperature SCR activity. K ions are suggested to interact with vanadium and tungsten species chemically, resulting in a poor redox property of catalyst. More importantly, potassium can reduce the Br?nsted acidity of catalysts and decrease the stability of Br?nsted acid sites significantly. The more severe deactivation of the KCl-treated catalyst can be mainly ascribed to the higher amount of potassium resided on catalyst.

关键词： V₂O₅-WO₃/TiO₂ potassium chloride poisoning reducibility acid sites

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POCl3sub> diffusion for industrial Si solar cell emitter formation

Hongzhao LI,Kyung KIM,Brett HALLAM,Bram HOEX,Stuart WENHAM,Malcolm ABBOTT

《能源前沿（英文）》 2017年第11卷第1期页码 42-51 doi: 10.1007/s11708-016-0433-7

摘要： POCl diffusion is currently the standard method for industrial n-type emitter fabrication. In this study, we present the impact of the following processing parameters on emitter formation and electrical performance: deposition gas flow ratio, drive-in temperature and duration, drive-in O flow rate, and thermal oxidation temperature. By showing their influence on the emitter doping profile and recombination activity, we provide an overall strategy for improving industrial POCl tube diffused emitters.

关键词： POCl₃ diffusion emitter recombination oxidation silicon

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催化氧化净化黄磷尾气中的磷和硫

宁平,Hans-JörgBart,王学谦,马丽萍,陈梁

《中国工程科学》 2005年第7卷第6期页码 27-35

摘要： KU2和活性炭都能通过催化氧化过程有效脱除黄磷尾气中的P4sub>，PH3sub>和H2sub>S杂质，随着反应温度和氧含量增加可显著提高净化效果，在最优条件下，经催化氧化净化后的总磷含量＜5mg/m³，硫化氢＜5mg/m³，失效后的催化剂易于再生，催化剂经多次再生后催化性能恢复良好；提出了活性炭固定床稳定流动吸附过程的数学模型

关键词：催化剂催化氧化 H2sub>S P4sub> PH3sub> 固定床

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Tuning nitrogen defects and doping sulfur in carbon nitride for enhanced visible light photocatalytic activity

《化学科学与工程前沿（英文）》 2023年第17卷第1期页码 93-101 doi: 10.1007/s11705-022-2175-x

摘要： Defect construction and heteroatom doping are effective strategies for improving photocatalytic activity of carbon nitride (g-C₃N₄). In this work, N defects were successfully prepared via cold plasma. High-energy electrons generated by plasma can produce N defects and embed sulfur atoms into g-C₃N₄. The N defects obviously promoted photocatalytic degradation performance that was 7.5 times higher than that of pure g-C₃N₄. The concentration of N defects can be tuned by different power and time of plasma. With the increase in N defects, the photocatalytic activity showed a volcanic trend. The g-C₃N₄ with moderate concentration of N defects exhibited the highest photocatalytic activity. S-doped g-C₃N₄ exhibited 11.25 times higher photocatalytic activity than pure g-C₃N₄. It provided extra active sites for photocatalytic reaction and improved stability of N defects. The N vacancy-enriched and S-doped g-C₃N₄ are beneficial for widening absorption edge and improving the separation efficiency of electron and holes.

关键词： g-C₃N₄ nitrogen defect sulfur doping photodegradation plasma

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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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Complete oxidation of methane on CoO-SnO catalysts

Xingfu TANG , Jiming HAO , Junhua LI ,

《环境科学与工程前沿（英文）》 2009年第3卷第3期页码 265-270 doi: 10.1007/s11783-009-0019-2

摘要： CoO-SnO hybrid oxides were prepared by the coprecipitation method and were used to oxidate methane (CH) in presence of oxygen. The CoO-SnO with a molar ratio of Co/(Co+Sn) at 0.75 exhibited the highest catalytic activity among all the CoO-SnO hybrid oxides. Experimental results showed that the catalysts were considerably stable in the CH combustion reaction, and were verified by X-ray photoelectron spectra (XPS). It was found that CoO was the active species, and SnO acted as a support or a promoting component in the CoO-SnO hybrid oxides. The surface area was not a major factor that affected catalytic activity. The hydrogen temperature-programmed reduction (H-TPR) results demonstrated that the interaction between cobalt and tin oxides accelerated the mobility of oxygen species of CoO-SnO, leading to higher catalytic activity.

关键词： Co₃O₄-SnO₂ complete oxidation methane (CH₄)

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过硫酸盐诱导的缺陷氮化碳中三配位氮（N3Csub>）空位增强光催化产过氧化氢 Article

缪蔚, 王奕杰, 刘莹, 秦贺贺, 褚成成, 毛舜

《工程（英文）》 2023年第25卷第6期页码 214-221 doi: 10.1016/j.eng.2021.12.016

摘要：其中石墨氮化碳（g-C3sub>N4sub>）被认为是最有前途的合成过氧化氢的光催化剂之一；并且，在g-C3sub>N4sub>中引入氮空位已被证明是提高其光催化活性的有效策略在此，本文提出了一种简便的过硫酸钠共晶聚合方法，制备了具有丰富三配位氮空位（N3Csub>）的g-C3sub>N4sub>。这种类型的氮空位在g-C3sub>N4sub>光催化产过氧化氢的研究中尚未得到重视。富含N3Csub>空位的g-C3sub>N4sub>的光催化过氧化氢产量是原始g-C3sub>N4sub>的4.5倍。本研究提出了在g-C3sub>N4sub>中引入N3Csub>空位的新策略，为开发光催化产过氧化氢的活性催化剂提供了一种新方法。

关键词：氮化碳 N3Csub>空位过氧化氢光催化过硫酸盐