Dielectric performance and conductive mechanism of KNN-based ceramics prepared via sol–gel core–shell process

Journal of Materials Science: Materials in Electronics - 0.95(Li0.02Na0.50K0.48)(Nb0.95Sb0.05)O3–0.05AgTaO3@BaZrO3 (LNKNbSAT@BZ) lead-free ceramics were prepared via a sol–gel...     

Extinction and Non-extinction of Solutions to a Fast Diffusion p-Laplace Equation with Logarithmic Non-linearity

This paper deals with a class of fast diffusion p-Laplace equation with logarithmic non-linearity in a bounded smooth domain with homogeneous Dirichlet boundary condition. By using energy estimates and some ordinary differential inequalities, we study the conditions on extinction and non-extinction of global solutions. The results of this paper extend and complete the previous studies on this equation.

     

Phosphorus-doped silicon nanoparticles as high performance LIB negative electrode

Journal of Materials Science - Silicon is getting much attention as the promising next-generation negative electrode materials for lithium-ion batteries with the advantages of abundance, high...     

依托"大数据行业应用"虚拟教研室培养跨学科人才

在实施国家大数据战略和创新型国家建设的引导下,培养跨学科思维与能力是创新型人才培养的核心要求.大数据是一个典型的学科交叉的技术,资源分散是当前高校大数据人才培养存在的主要问题.该文以长沙理工大学"大数据行业应用"虚拟教研室建设为例,打造"大数据"特色跨学科跨专业教学组织,从课程体系、实践环节、师资队伍、质量监督等方面提出建设措施,为培养跨学科创新型复合型人才提供参考.     

双功能催化剂上四氢萘加氢裂化生成单环芳烃的反应网络研究

Conversion of LCO (light cycle oil) to BTX (benzene, toluene, and xylene) is an economically valuable method for refineries. However, this approach still faces difficulties as the main reactions are not clearly understood. Here we study the detailed hydrocracking pathway of typical reactants, 1-methylnaphthalene and tetralin, through molecular simulations and experiments to improve our understanding of the conversion process of LCO to BTX. Molecular simulations demonstrate that the rate-determining step is the isomerization pathway of six-membered ring to five-membered ring in tetralin as its activation energy (ΔEa) is the highest among all the reactions and the order of ΔEa of reactions is isomerization > ring-opening ≈ side-chain cleavage. The results of experiments show that with the increase in reaction depth, i.e., through a high temperature (350 – 370 °C) and low LHSV (4.5 – 6.0 h−1), isomerization, ring-opening, and side-chain  cleavage reactions occurred, thus improving the selectivity and yield of alkyl aromatics.