Institution
Beijing Institute of Petrochemical Technology
Education•Beijing, China•
About: Beijing Institute of Petrochemical Technology is a education organization based out in Beijing, China. It is known for research contribution in the topics: Catalysis & Corrosion. The organization has 2468 authors who have published 1937 publications receiving 19270 citations.
Topics: Catalysis, Corrosion, Coating, Welding, Adsorption
Papers published on a yearly basis
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Abstract: There has recently been a dramatic renewal of interest in hadron spectroscopy and charm physics. This renaissance has been driven in part by the discovery of a plethora of charmonium-like XYZ states at BESIII and B factories, and the observation of an intriguing proton-antiproton threshold enhancement and the possibly related X(1835) meson state at BESIII, as well as the threshold measurements of charm mesons and charm baryons. We present a detailed survey of the important topics in tau-charm physics and hadron physics that can be further explored at BESIII during the remaining operation period of BEPCII. This survey will help in the optimization of the data-taking plan over the coming years, and provides physics motivation for the possible upgrade of BEPCII to higher luminosity.
296 citations
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TL;DR: C1 chemistry and the design of highly selective new catalysts for high-value chemicals are enriched and the electronic structure of the catalyst surface suppresses the hydrogenation of double bonds and promotes desorption of products, which renders the catalyst unexpectedly reactive toward alkenes.
Abstract: Zn- and Na-modulated Fe catalysts were fabricated by a simple coprecipitation/washing method. Zn greatly changed the size of iron species, serving as the structural promoter, while the existence of Na on the surface of the Fe catalyst alters the electronic structure, making the catalyst very active for CO activation. Most importantly, the electronic structure of the catalyst surface suppresses the hydrogenation of double bonds and promotes desorption of products, which renders the catalyst unexpectedly reactive toward alkenes-especially C5+ alkenes (with more than 50% selectivity in hydrocarbons)-while lowering the selectivity for undesired products. This study enriches C1 chemistry and the design of highly selective new catalysts for high-value chemicals.
296 citations
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TL;DR: In this article, the authors focused on the removal of arsenic from water using iron-based materials, such as iron nanoparticles, layered double hydroxides (LDHs), zero-valent iron (ZVI), iron-doped activated carbon, iron-depleted polymer/biomass materials, and iron-containing combined metal oxides.
Abstract: Intensive research efforts have been pursued to remove arsenic (As) contamination from water with an intention to provide potable water to millions of people living in different countries. Recent studies have revealed that iron-based adsorbents, which are non-toxic, low cost, and easily accessible in large quantities, offer promising results for arsenic removal from water. This review is focused on the removal of arsenic from water using iron-based materials such as iron-based nanoparticles, iron-based layered double hydroxides (LDHs), zero-valent iron (ZVI), iron-doped activated carbon, iron-doped polymer/biomass materials, iron-doped inorganic minerals, and iron-containing combined metal oxides. This review also discusses readily available low-cost adsorbents such as natural cellulose materials, bio-wastes, and soils enriched with iron. Details on mathematical models dealing with adsorption, including thermodynamics, kinetics, and mass transfer process, are also discussed. For elucidating the adsorption mechanisms of specific adsorption of arsenic on the iron-based adsorbent, X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) are frequently used. Overall, iron-based adsorbents offer significant potential towards developing adsorbents for arsenic removal from water.
275 citations
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TL;DR: The use of macro plastic fibres to reinforce concrete has attracted widespread attention from both scientists and construction industry due to the multiple sustainability benefits they offer, compared to steel fibres and steel reinforcing mesh as mentioned in this paper.
272 citations
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TL;DR: The prepared SFMNi material is a promising high-performance anode for solid oxide fuel cells and shows excellent structural stability and good coking resistance in wet CH4.
Abstract: A metallic nanoparticle-decorated ceramic anode was prepared by in situ reduction of the perovskite Sr2FeMo0.65Ni0.35O6−δ (SFMNi) in H2 at 850 °C. The reduction converts the pure perovksite phase into mixed phases containing the Ruddlesden–Popper structure Sr3FeMoO7−δ, perovskite Sr(FeMo)O3−δ, and the FeNi3 bimetallic alloy nanoparticle catalyst. The electrochemical performance of the SFMNi ceramic anode is greatly enhanced by the in situ exsolved Fe–Ni alloy nanoparticle catalysts that are homogeneously distributed on the ceramic backbone surface. The maximum power densities of the La0.8Sr0.2Ga0.8Mg0.2O3−δ electrolyte supported a single cell with SFMNi as the anode reached 590, 793, and 960 mW cm–2 in wet H2 at 750, 800, and 850 °C, respectively. The Sr2FeMo0.65Ni0.35O6−δ anode also shows excellent structural stability and good coking resistance in wet CH4. The prepared SFMNi material is a promising high-performance anode for solid oxide fuel cells.
263 citations
Authors
Showing all 2499 results
Name | H-index | Papers | Citations |
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J. S. Lange | 160 | 2083 | 145919 |
Chao Zhang | 127 | 3119 | 84711 |
S. J. Chen | 116 | 1559 | 62804 |
Y. Ban | 104 | 1346 | 49897 |
Min Zhang | 85 | 1548 | 34853 |
Shan Jin | 83 | 365 | 37419 |
Y. J. Mao | 81 | 829 | 29089 |
Lei Zhang | 78 | 1485 | 30058 |
Jialun Ping | 73 | 676 | 22314 |
Li Li | 67 | 855 | 22796 |
D. Y. Wang | 64 | 637 | 18612 |
M. Qi | 58 | 466 | 19175 |
J. G. Messchendorp | 54 | 593 | 12498 |
Xiangming He | 52 | 480 | 10801 |
Nasser Kalantar-Nayestanaki | 51 | 691 | 11500 |