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本着培养涂料行业精英人才的宗旨,针对涂料行业对人才需求的特点,结合多年教学经验,从教材的选择、教学内容设置、教学方法改进以及考核方法改革等4个方面探索了“功能涂料”课程的教学方法改革与课程实践。通过自编教材,精心设置授课内容,将科研成果、前沿知识、生活场景、新闻事件与书本知识相结合,提高课堂的趣味性;通过讨论法和交换式互动上课来加强课堂的互动性;通过过程性评价提高课程的学业挑战度。通过教学改革,本课程的选课率和出勤率得到了大幅提高,学生对涂料的兴趣明显增加,毕业后选择进入涂料领域工作的学生也越来越多。 相似文献
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新工科背景下,创新实践能力的培养已经成为高校人才培养工作的重点。仪器分析作为科学研究的眼睛,内容涉及诸多领域,体现多学科交叉的全局思想观和方法论,对人才创新实践能力培养具有重要作用。针对仪器分析课程教学凸显的诸多痛点问题,课程组坚持“以生为本,立德树人,思创融合,知行合一”的教改理念,构建了以学生创新实践能力塑造为导向的课程教学目标和三维评价体系,采用显性知识与隐性价值观相融合、线上与线下相融合、问题驱动与可视化教学相融合、理论学习与研究实践相融合的四轮融合教学模式创新实践。实践证明,新的教学模式极大地激发了学生的学习兴趣和求知欲望,在课程成绩大幅提高的同时,学生的综合创新实践能力也得到了很好的塑造。 相似文献
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通过对课程的定位,教学资料的规范化、系列化、系统化和多媒体化,MCAI课件和计算机模拟软件的制作,网络的利用,以及多种媒体的组合教学,对多方位的多媒体计算机辅助高分子物理教学进行了研究与实践;为培养基础扎实、知识面宽、能力强、素质高的人才提供了一种切实有效的教学方案;并将课程建设推上了一个新台阶。 相似文献
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Jun Sakamoto Takashi Nakagawa Nobuko Kanehisa Yasushi Kai Masahiro Katsura 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(9):e411-e412
In the title compounds, C4H8N2O2, (I), and C5H10N2O2, (II), respectively, the amide groups are rotated out of the central C—C—C plane by ca 76° in (I) and by 70–73° in (II). Compound (I) has crystallographic mirror symmetry perpendicular to the molecular plane. 相似文献
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Kerstin Schulze‐Matthi Jürgen Bendig Petra Neubauer Burkhard Ziemer 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(6):e257-e258
The bonding geometry of sulfur in the cations of the title compounds, C8H11S+·CF3SO3? and C13H13S+·CF3SO3?, respectively, is similar and is independent of the ratio of the Me/Ph substituents. As expected, in both cations, the S—Ph bonds are somewhat shorter than the S—Me bonds. In both crystal structures, the interaction between cations and anions is similar. 相似文献
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M. Donaldson Rebecca Stevens B. E. Lang Juliana Boerio-Goates B. F. Woodfielda R. L. Putnam Alexandra Navrotsky 《Journal of Thermal Analysis and Calorimetry》2005,81(3):617-625
Summary As part of a larger study of the physical properties of potential ceramic hosts for nuclear wastes, we report the molar heat capacity of brannerite (UTi2O6) and its cerium analog (CeTi2O6) from 10 to 400 K using an adiabatic calorimeter. At 298.15 K the standard molar heat capacities are (179.46±0.18) J K-1 mol-1 for UTi2O6 and (172.78±0.17) J K-1 mol-1 for CeTi2O6. Entropies were calculated from smooth fits of the experimental data and were found to be (175.56±0.35) J K-1 mol-1 and (171.63±0.34) J K-1 mol-1 for UTi2O6 and CeTi2O6, respectively. Using these entropies and enthalpy of formation data reported in the literature, Gibb’s free energies of formation from the elements and constituent oxides were calculated. Standard free energies of formation from the elements are (-2814.7±5.6) kJ mol-1 for UTi2O6 and (-2786.3±5.6) kJ mol-1 for CeTi2O6. The free energy of formation from the oxides at T=298.15 K are (-5.31±0.01) kJ mol-1 and (15.88±0.03) kJ mol-1 for UTi2O6 and CeTi2O6, respectively. 相似文献
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Jose G. Trujillo‐Ferrara Efrn V. García‐Bez Itzia I. Padilla‐Martínez Francisco J. Martínez‐Martínez Norberto Farfan‐García 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(6):o427-o430
In exo‐2‐(3,5‐dioxo‐10‐oxa‐4‐azatricyclo[5.2.1.02,6]dec‐8‐en‐4‐yl)phenyl acetate, C16H13NO5, the plane of the acetoxy group lies almost perpendicular to that of the phenyl ring [dihedral angle = 89.8 (1)°], in contrast with the smaller deviations found in the para isomer exo‐4‐(3,5‐dioxo‐10‐oxa‐4‐azatricyclo[5.2.1.02,6]dec‐8‐en‐4‐yl)phenyl acetate, C16H13NO5, these being 63.6 (1) and 37.0 (1)° for the two crystallographically independent molecules. Irrespective of the position of the acetoxy group, both compounds pack through soft C—H⋯X (X is O or phenyl) interactions, forming interlinked centrosymmetric tetramers in the bc plane. 相似文献
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Nikolina L. Petrova Dimitar S. Todorovsky Veselinka G. Vasileva 《Central European Journal of Chemistry》2005,3(2):263-278
Mn-, LaMn- and LaCaMn-citrates were synthesized at 60–120°C in ethylene glycol medium using chlorides or nitrates as metal
sources. Their composition, IR spectra and thermal decomposition were studied. Equimolar La/Mn ratio has been established
in the complex, prepared from chloride solution with the same initial composition of the metals. In the isolated three-metallic
complex the molar ratio of the metals deviates from the composition in the initial solution. The final products of the heating
of Mn- and mixed-metal LaMn-citrates at 1000°C are phase-homogeneous Mn3O4 (hausmannite) and LaMnO3 respectively. Parasitic phase(s) are observed in LaxCa1−xMnyO3, produced from LaCaMn-citrate. 相似文献
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Maren Pink Doyle Britton Wayland E. Noland Matthew J. Pinnow 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(10):1271-1273
The molecular structures of the title compounds, 2,4,6‐trichlorophenylisonitrile (IUPAC name: 2,4,6‐trichlorophenyl isocyanide), C7H2Cl3N, and 2,4,6‐trichlorobenzonitrile, C7H2Cl3N, are normal. The two structures are not isomorphous, but do contain similar two‐dimensional layers in which pairs of molecules are held together by pairs of Cl?CN [3.245 (3) Å] or Cl?NC [3.153 (2) Å] interactions. The two‐dimensional isomorphism is lost through different layer‐stacking modes. 相似文献
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A. N. Enyashin V. V. Ivanovskaya I. R. Shein Yu. N. Makurin N. I. Medvedeva A. A. Sofronov A. L. Ivanovskii 《Journal of Structural Chemistry》2004,45(4):547-556
Atomic models of achiral NbSe2 nanotubes are suggested. Band structure calculations have been performed to investigate the electronic structure and determine the parameters of interatomic interactions. The distribution of the density of states and pair bond occupancies of NbSe2 nanotubes are analyzed in relation to the type of the atomic configuration and the tube diameter; the results are compared with the band structure of the 2H-NbSe2 crystal. Calculations have been carried out on hypothetical superstoichiometric nanotubes with a formal composition Nb1.25Se2 as possible quasi-one-dimensional nanoforms of autointercalated niobium diselenide.Original Russian Text Copyright © 2004 by A. N. Enyashin, V. V. Ivanovskaya, I. R. Shein, Yu. N. Makurin, N. I. Medvedeva, A. A. Sofronov, and A. L. IvanovskiiTranslated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 4, pp. 579–588, July–August, 2004.This revised version was published online in April 2005 with a corrected cover date. 相似文献
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Magorzata Hoyska Tadeusz Lis 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(12):m648-m650
Ethyltriphenylphosphonium perrhenate, (C20H20P)[ReO4], and (iodomethyl)triphenylphosphonium perrhenate, (C19H17IP)[ReO4], have been crystallized from 2‐propanol. Both crystal structures consist of phosphonium cations and perrhenate anions. The cations show the typical propeller‐like geometry. In both crystals, the positions of the nearly tetrahedral anions are stabilized by weak C—H⋯O hydrogen bonds, and for the latter compound, I⋯π interactions also occur. 相似文献
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Eu3+ ion-doped LaPO4 nanowires or nanorods have been successfully synthesized by a simple hydrothermal method. The influence of varying the hydrothermal
and subsequent sintering conditions on the morphology and structure of the LaPO4 host has been investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD). For comparison, the Eu3+ ions were also doped into monoclinic monazite LaPO4 nanoparticles and perovskite LaAlO3 nanoparticles. The relative intensities of the emission lines of the LaPO4:Eu3+ nanosystems were essentially independent of their shape. The optimal doping concentrations in the monoclinic LaPO4 and perovskite LaAlO3 nanosystems were determined to be about 5.0 and 3.5 mol%, respectively. Under appropriate UV-radiation, the red light emitted
from LaAlO3:Eu3+ (3.5 mol%) was brighter than that from LaPO4:Eu3+ (5.0 mol%) nanomaterial, resulting from differences in their spin-orbit couplings and covalence, which indicates that the
nanoscale LaAlO3 is a promising host material for rare earth ions.
Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.
Supported by the National Natural Science Foundation of China (Grant Nos. 20873039 & 90606001), Hunan Provincial Natural Science
Foundation (No. 07jj4002), and the Students Innovation Training Fund of Hunan University 相似文献
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Fe3O4 nanorods and Fe2O3 nanowires have been synthesized through a simple thermal oxide reaction of Fe with C2H2O4 solution at 200–600°C for 1 h in the air. The morphology and structure of Fe3O4 nanorods and Fe2O3 nanowires were detected with powder X-ray diffraction, scanning electron microscopy and transmission electron microscopy.
The influence of temperature on the morphology development was experimentally investigated. The results show that the polycrystals
Fe3O4 nanorods with cubic structure and the average diameter of 0.5–0.8 μm grow after reaction at 200–500°C for 1 h in the air.
When the temperature was 600°C, the samples completely became Fe2O3 nanowires with hexagonal structure. It was found that C2H2O4 molecules had a significant effect on the formation of Fe3O4 nanorods. A possible mechanism was also proposed to account for the growth of these Fe3O4 nanorods.
Supported by the Fund of Weinan Teacher’s University (Grant No. 08YKZ008), the National Natural Science Foundation of China
(Grant No. 20573072) and the Doctoral Fund of Ministry of Education of China (Grant No. 20060718010) 相似文献