地方特色思政元素双向挖掘与实施*——以“无机化学”课程为例

以正向、逆向双向挖掘贴近学生现实生活的“三线精神”思政元素为例,介绍本教学团队双向挖掘地方特色思政元素,打造一门更生动,专业教育与思政教育同向同行、有机融合、协调育人的无机化学课程的实施过程。     

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。     

思政元素融入无机化学的教学初探

针对推进课程思政建设的重要性,阐明无机化学教学中融入思政元素的意义。结合笔者课程思政的教学实例,提出在日常教学中融入思政元素的策略和相关教学改革的举措,并对专业教师素质提出了要求。     

无机化学及无机化学实验中的思政元素

无机化学及无机化学实验是化学专业学生最先接触到的专业基础课。本文梳理了这两门课程中专业知识与思政元素的结合点,并着重从培养学生的思辨精神和科学发展观、社会责任感和担当及"爱国、敬业、诚信、友善"的价值观这三方面来说明课程思政在育人中的重要性。     

能源化学工程专业的无机化学课程思政特色建设

对能源化学工程专业无机化学课程的课程思政建设进行了系统的设计、探索与实践。主要举措包括从能源化学工程专业视角充分挖掘无机化学的课程思政元素，采用绪论引领、随堂引入或引导、案例研讨、专题分享、在线推文和交流等方式进行课程思政教育，实现全程和全方位促学，激发学生的专业使命感和社会责任感，提升了学生的综合能力和专业素养。     

传统文化蕴含的化学智慧在元素无机化学教学中的有机融入

在讲授元素无机化学时,把中国传统文化中所包含的化学知识、化学智慧有机地融入课堂教学,将元素无机化学讲授与课程思政教学有机融合,从而增加理科课堂的文化性、知识性和趣味性,激发学生的学习兴趣;同时培养学生的文化自信,激发学生的民族自豪感。     

无机化学"课程思政"教学设计案例研究——以绪论教学为例

为深入贯彻落实习总书记在全国高校思想政治工作会议上的重要讲话精神,构建将思想政治理论课与各类课程同行同向的协同育人模式,探讨了课程思政育人的重要实践.本文以无机化学课程的"绪论"一课作为教学设计案例,从学习目标设置、教学内容选择与呈现、思政元素挖掘融合及教学活动的开展等方面探讨了课程思政在无机化学绪论课中有机融合的教学设计思路与方法.     

药学专业无机化学“课程思政”教学初探

课程思政教学理念有利于发挥高校"立德树人"的根本任务与教师"教书育人"的首要职责。本文通过多个视角梳理无机化学课程所蕴含的思政教育元素,将之融入课堂教学,以实现专业知识教育与思政教育的有机统一。     

无机元素化学的智慧“教与学”*

依托校内无机化学在线课程,将基于“超星”学习通平台的混合式教学模式引入元素化学知识的学习,设计了“MOOC+案例精讲+QQ群辅助”的教学策略。实践过程中,借助MOOC自主学习低阶的知识点,采用专题直播、分组活动、PBL教学法开展高阶知识点的学习,QQ群辅助进行实时答疑。学习通平台串联起了教室端、移动端和管理端,师生线上线下的交流互动,有助于实现愉快、高效的智慧“教与学”。调查显示,基于“一平三端”的混合教学形式得到大部分学生的认可。     

改革“试管实验”

近年来在工科院校无机化学实验课的改革中,出现了测定实验受到偏爱,“试管实验”遭到冷落的倾向。我们认为在无机化学实验课中,“试管实验”应占有一定的地位。因为: 1.元素化学应是本课程的中心内容之一,元素及化合物的性质实验应是无机化学     

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.     

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.     

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.     

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.     

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.     

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)     

Electrochemical and magnetic characterization of LiFePO<Subscript>4</Subscript> and Li<Subscript>0.95</Subscript>Mg<Subscript>0.05</Subscript>FePO<Subscript>4</Subscript> cathode materials

A series of lithium iron phosphates was synthesized via the sol–gel route. Iron phosphides, which are electronic conductors, were formed when sintered at 850°C. Magnetic susceptibility measurements on the samples show antiferromagnetic behaviour with T _N=50±2 K for LiFePO₄ and Li_0.95Mg_0.05PO₄ sintered at temperatures below 850°C. The LiFePO₄ and Li_0.95Mg_0.05FePO4 cathodes show a stable electrochemical capacity in the range of 150–160 mA h/g on cycling. The cyclability deteriorates with increasing sample sintering temperature due to the increased crystal size and impurities.