“化学海洋学实验”课程的建设和教学实践

作为海洋化学专业的实践课程,“化学海洋学实验”已在很多高校开设,但该课程目前在授课内容、教学大纲和教学方法等方面尚未统一。在分析了该课程目前存在问题的基础上,介绍了中国海洋大学相关课程教学团队在该实验课程建设方面采取的措施,包括更新了课程的设计理念,调整、充实了实验内容,编写了实验教材,并介绍了学生通过学习该课程得到的锻炼和可以达到的学习目的。该课程的建设经验和教学实践对于课程的推广应用,以及培养知识结构合理、实践能力强的海洋人才,具有重要的作用。     

大学基础有机化学双语教学实践的总结与反思

双语教学是培养具有国际视野和国际竞争力人才的重要举措。对基础有机化学10年来的双语教学实践进行了认真的总结和反思,内容包括该课程的教学团队、使用教材、选课学生、教学手段、教学策略、教学多媒体平台建设等方面。     

面向高阶思维培养的自主型实验教学模式的设计与实践*

基于教育现代化、发展“互联网+教育”、培养创新性人才的指导思想,结合“超星学习通”网络平台与实验课堂的优势,设计了面向高阶思维培养的“预习自测-讲授讨论-自主实践-总结反思”的四段自主型实验教学模式,并应用于化学与化工类专业分析化学实验课程的教学实践。该实验教学模式增加了学生自主学习时间,培养了学生“分析、综合、评价和创造”等高阶思维能力,提高了实验课程的教学效率,为高等院校实践实验教学的改革提供了参考依据。     

“功能涂料”课程的教学改革:打造趣味性、互动性和挑战性的课堂*

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。     

面向创新实践能力培养的仪器分析四轮融合教学创新

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。     

多媒体计算机辅助高分子物理教学的研究与实践

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。     

仪器分析综合运用及创新能力的培养——浅谈仪器分析实践教学体系的构建

以数年仪器分析课程教学经验为基础,以培养具有实践能力和创新能力、符合社会需求的复合型应用人才为目标,以专业实际情况为出发点,介绍东北林业大学化学工程与工艺专业仪器分析实践课程体系的构建。     

无机化学教学中“课程思政”教育的探索与实践

结合无机化学特点,分析专业课教学中开展"课程思政"存在的问题,讨论如何挖掘无机化学课程所蕴含的思想政治教育元素,探索思想政治教育融入无机化学课程的实践途径,提出在专业课教学过程中,通过典型案例融入思政元素的具体方法,以实现价值引领、能力培养和知识传授的"三位一体"教育目标,培养德才兼备的高素质人才。     

化工原理项目设计教学改革的实践与成效

通过对化工原理的项目设计理念、项目层级关系、项目结构、设计内容、评价方法、实践效果的梳理,阐述了以工程项目设计为牵引,工程实践能力和创新能力高素质人才培养为目标,进行化工原理项目设计教学改革与创新的具体做法。以OBE理念和CDIO课程体系建设为基础,强调人才特色培养、课程结构优化的实践教学课程改革,加深了对化工原理项目设计的认识。     

贯穿论文式实验报告的综合能力培养教学实践

加强实验教学是培养学生科学素养和综合创新能力的重要途径。基于"两性一度"的课程教学要求,针对目前实验教学中撰写实验报告存在的问题,以物理化学实验课程为例,进行了教学改革与实践。采取贯穿科研论文式实验报告撰写各环节的科学素养和能力培养模式,该论文式实验报告有利于学生整体把握,提出问题、分析问题和总结,实验报告的各个部分与实际教学环节相统一,取得了满意的效果。充分发挥了教师主导和学生主体的协同优势,激发了学生学习的积极性和主观能动性,有利于培养德智体美劳全面发展的高素质人才。     

Methyl­malon­amide and ethyl­malon­amide

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.     

Di­methyl­phenyl­sulfonium tri­fluoro­methane­sulfonate and methyl­di­phenyl­sulfonium tri­fluoro­methane­sulfonate

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.     

Heat capacities and absolute entropies of UTi<Subscript>2</Subscript>O<Subscript>6</Subscript> and CeTi<Subscript>2</Subscript>O<Subscript>6</Subscript>

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.     

Exo Diels–Alder adducts between ortho‐ and para‐N‐acetoxy­phenyl­male­imides and furan

In exo‐2‐(3,5‐dioxo‐10‐oxa‐4‐aza­tri­cyclo­[5.2.1.0^2,6]­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[5.2.1.0^2,6]­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.     

Synthesis and characterization of Mn-, La-Mn- and La-Ca-Mn-citrates as precursors for LaMnO<Subscript>3</Subscript> and La<Subscript>1−x</Subscript>Ca<Subscript>x</Subscript>MnO<Subscript>3</Subscript>

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 La_xCa_1−xMn_yO₃, produced from LaCaMn-citrate.     

2,4,6‐Tri­chloro­phenyl­iso­nitrile and 2,4,6‐tri­chloro­benzo­nitrile

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.     

Interatomic interactions and electronic structure of NbSe<Subscript>2</Subscript> and Nb<Subscript>1.25</Subscript>Se<Subscript>2</Subscript> nanotubes

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 Nb_1.25Se₂ 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.     

Ethyl­tri­phenyl­phospho­nium perrhenate and (iodo­methyl)­tri­phenyl­phospho­nium perrhenate

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.     

Eu<Superscript>3+</Superscript>-doped LaPO<Subscript>4</Subscript> and LaAlO<Subscript>3</Subscript> nanosystems and their luminescence properties

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     

Thermal oxide synthesis and characterization of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanorods and Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> nanowires

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)