化工类专业课教学中开展爱国主义教育的探索*——以“节能减排与国家利益”专题教学为例

在“课程思政”背景下,如何在化工类专业课教学中开展爱国主义教育,是一大挑战。将节能减排所涉及的专业知识作为载体,引入“碳排放”议题作为思政素材,引导学生运用专业知识来解读该议题,将爱国主义元素“无声”地融入专业课教学中。通过解析美国在该议题背后的真实目的和我国的应对策略,激发学生的爱国热情,并使之认识到党在维护国家发展利益方面的决心和能力;通过探寻新中国不同时期的重大历史事件与“碳排放”走势的关联性,使学生深刻认识中国共产党带领中国人民选择了一条正确的道路。本专题教学将专业知识与“思政”元素深度融合,实现了爱国、爱党和爱社会主义3者的统一,对同行教育工作者具有一定的借鉴意义。     

“三端合一”显隐结合的无机化学课程思政方法*

基于本校无机化学的课程特色,拟定课程思政目标,将思政元素与教学内容对应。在无机化学课程的资源端(MOOC平台)、教学端(超星学习通)、服务端(微信公众号)等均融入思政元素,创新教学方法,构建“三端合一”显隐结合的课程思政方法,为其他专业课的课程思政提供参考。     

SPOC教学模式下课程思政教学设计与实践*——以无机及分析化学课程思政教学改革为例

依托SPOC的“自主学习+合班授课+小班讨论”教学模式,在对课程思政元素进行梳理和提炼的基础上,将思政元素融入到SPOC教学的全过程,通过“三结合”的教学方式形成本课程的教学特色。学生无记名问卷调查统计结果表明,在SPOC教学模式下开展课程思政教学是完全可行的,取得了良好的教学效果,学生满意度非常高。     

材料化学课程思政的探索与实践*——以“常见金属材料”为例

以“金属材料”中的“常见金属材料”为例,从教学内容和教学评价2个方面探讨了材料化学课程的思政教学。从铝合金、铜合金、钢铁等几种常见金属材料的生产、应用等方面将教学内容与思政元素有机融合,在教学评价中融入思政教育,增强学生的创新创业意识、环境保护意识、资源保护意识、民族自豪感和社会责任感,践行“立德树人”的教育理念。     

药物化学课程思政教学模式的探索与实践*——青霉素抗生素专题

药物化学是药学专业核心课程,拥有丰富的思政资源。以药物化学课程为研究对象,在明确课程思政育人目标基础上,将药物化学课程思政教学主线设置为“定目标、拆内容、寻热点、挖元素、隐融入、明效果、做评价”等7个环节。进一步以青霉素专题为例,展示思政内容有机融入课程教学的全过程,为其他理工类专业课程思政教学提供一种参考模式。     

化学专业概论教学中的课程思政探索与实践*——以华中科技大学“一院一品”化学专业概论课为例

课程思政是高校落实立德树人根本任务的重要举措,是完善“三全育人”的重要抓手。化学是我国科学研究的重要基础,对提升原始创新能力具有重要意义。化学专业教学中融入思想政治教育的前提是建设好一门课程。针对当前专业课教学中存在的课程思政体系不完善、思政元素与专业课程融合程度低、教师思政教学水平有待提高等问题,以华中科技大学化学与化工学院专业概论课为试点,完善课程设计与教学方法,探索化学专业教学中的课程思政建设。通过剖析化学课程思政的意义与难点,构建专业概论课实施方案,形成一套行之有效的化学课程思政建设体系。     

课程思政背景下大学基础有机化学实验教学探索与实践*

从大学基础有机化学实验“课程思政”建设背景出发,讨论了课程思政的育人目标、实验教学中如何融入课程思政、课程思政的建设策略以及课程思政实施与考核评价方式等方面。结合实验教学过程探讨了基础有机化学实验教学中融入课程思政的教学探索和实践。     

课程思政下化学教学论逆向教学设计*——以“说课”为例

阐述了化学教学论课程思政开展思路和逆向教学设计的基本阶段、价值意蕴。逆向教学设计以预期目标为起点,是助力课程思政进展的有效举措。以“说课”为例,探索了课程思政理念下逆向教学设计“设定预期成果—确定评估证据—计划教学指导方案”三阶段规划,并进行了教学过程设计和教学反思。逆向教学设计中教学内容甄选、教学活动设置、教学评价等都指向教学目标,有利于课程育人功能的发挥。     

化学实验“三三三”翻转教学模式的探索与实践*

针对当前化学实验翻转课堂教学模式中存在的不足,依托“云班课”,重构了以学生为中心的化学实验“三三三”翻转教学新模式,即将实验教学划分为“三个课堂”:自学课堂、理论课堂和实验课堂等;理论课堂里包含“三个环节”:个人汇报、小组活动和测试点评等;学习效果评判有“三个评价”:自学评价、参与评价和动手评价等。以有机化学实验中“环己烯的合成”为例,采用该新的教学模式开展了教学活动,整个教学过程不仅体现了“以学定教、学生为中心”的教学理念,而且也能发挥出线下传统课堂的优势,实现了将“知识内化”的时间拉长,达到对学生线上自学“知识传授”掌握度的有力检验的目的,更有时间和空间进行课程思政元素的挖掘与融入,完成在知识传播中实现对学生的价值引领。     

师范院校有机化学教学融入课程思政的探索与实践*

通过有机化学的教学探索与实践,着力构建三维课程思政建设体系,让“课程思政”进课前、驻课中、留课后,挖掘有机化学思政元素、构建课程思政案例库,并在探索与实践中实施教学效果调查、跟踪学生发展、深化反思总结,努力发挥有机化学教学融入课程思政的积极成效,实现通过有机化学专业课程的教与学来达到育人目的,助力培养卓越未来教师。     

Ab initio studies of the conformations of ethynyl formate, cyano formate and related ethynyl and cyano compounds

The optimized geometries, relative free energies and related thermodynamic properties, harmonic frequencies, and dipole moments have been calculated at the HF and MP2 levels for ethynyl formate (1a), ethynyl acetate (1b), cyano formate, HCO₂CN (1c), cyano acetate (1d), S-ethynyl thioformate (2a), S-ethynyl thioacetate (2b), S-cyano thioformate (2c), S-cyano thioacetate (2d), N-ethynylformamide (3a), N-ethynylacetamide (3b), N-cyanoformamide (3c), and N-cyanoacetamide (3d) with the gaussian 98 program. For ethynyl formate, the calculation for 25 °C at the MP2/6-311++G(df,pd) level predicts that the Z isomer is more stable by 1.23 kcal/mol. For S-ethynyl thioformate, calculations at the MP2/6-311++G(2d,2p) level predict that the E isomer is favored by 0.71 kcal/mol at 25 °C. The E isomers of N-ethynylformamide and N-ethynylacetamide were found at all levels to be more stable than the Z isomers at 25 °C. For cyano formate and cyano acetate, calculations at the MP2/6-311++G(df,pd) level predict that the Z isomers are more stable at 25 °C by 1.50 and 2.72 kcal/mol, respectively. At this level and temperature, the Z isomers of 2c, 2d, 3c, and 3d are predicted to have free energies of 0.46, −0.07, 1.22, and 2.28 kcal/mol, respectively, relative to the E conformations. Z to E free-energy barriers at 25 °C of 8.63, 10.64, 17.63, 7.39, and 14.03 kcal/mol were calculated for 1a, 2a, 3a, 1c, and 3c at the HF/6-311G(d,p) level, and at the HF/6-311+G(d,p) level, the free-energy barrier for 2c was 7.08 kcal/mol.     

Alpha and gamma spectrometry for determination of natural and artificial radionuclides in tea, herbal tea and camomile marketed in Italy

Several kinds of tea, camomile and herbal tea were analysed to determine natural and artificial radioactivity. The radionuclides were determined by alpha (²¹⁰Po) and gamma (²²⁸Ac, ²¹⁴Pb, ²¹⁴Bi, ²¹⁰Pb, ⁴⁰K and ¹³⁷Cs) spectrometry. ²²⁸Ac ranged between 0.6 and 9.0 Bq kg⁻¹_dry; ²¹⁰Po between 1.90 and 36.1 Bq kg⁻¹_dry; ²¹⁴Pb and ²¹⁴Bi between 0.7 and 4.9 Bq kg⁻¹_dry; ²¹⁰Pb between < 10.0 and 58.9 Bq kg⁻¹_dry; ⁴⁰K between 463 and 936 Bq kg⁻¹_dry; ¹³⁷Cs between < 0.3 and 2.6 Bq kg⁻¹_dry. The percentage of ²¹⁰Po extraction in infusion was also determined; the arithmetical mean value of percentage of ²¹⁰Po extraction resulted 20.7 ± 7.50.     

元素医学防治心脑血管病研究和应用

从心脑血管疾病的流行率、心脑血管疾病的元素病因、心脑血管疾病的元素诊断和心脑血管疾病的元素治疗等4个方面讨论了元素医学防治心脑血管疾病的临床意义。     

Determination of low level nitrite and nitrate in biological, food and environmental samples by gas chromatography-mass spectrometry and liquid chromatography with fluorescence detection

Gas chromatography-mass spectrometry (GC-MS) and liquid chromatography with fluorescence detection (LC-FL) methods have been proposed for the determination of low level nitrite and nitrate in biological, food and environmental samples. The methods include derivatization of aqueous nitrite with 2,3-diaminonaphthalene (DAN), enzymatic reduction of nitrate to nitrite, extraction with toluene and chromatographic analyses of highly fluorescent 2,3-naphthotriazole (NAT) derivative of nitrite by using GC-MS in selected-ion-monitoring (SIM) mode and LC-FL. Nitrite and nitrate ions in solid samples were extracted with 0.5 M aqueous NaOH by sonication. The recoveries of nitrite and nitrate ions based on GC-MS and LC-FL results were 98.40% and 98.10% and the precision of these methods, as indicated by the relative standard deviations (RSDs) were 1.00% for nitrite and 1.20% for nitrate, respectively. The limits of detection of the GC-MS in SIM mode and LC-FL methods based on S/N = 3 were 0.02 and 0.29 pg/ml for nitrite and 0.03 and 0.30 pg/ml for nitrate, respectively.     

软硬酸碱规则与体内微量元素

阐述了ＳＨＡＢ规则,分类,酸碱软硬度的定量标度和理论解释。根据ＳＨＡＢ规则把体内微量元素分为Ｌｅｗｉｓ硬酸,软酸与交界酸和硬碱,软碱与交界碱,体内不同体液和器官含有丰富的软硬配体,与各类软硬酸（金属离子）结合成不同稳定性的配合物,发挥其生物活性作用。     

Potentiometric and thermodynamic studies of 2-mercapto-5-(2-hydroxynaphthylideamino)-1,3,4-thiadiazole and its metal complexes

Summary Proton-ligand dissociation constant of 2-mercapto-5-(2-hydroxynaphthylideamino)-1,3,4-thiadiazole (MHT) and the stepwise stability constants of its metal complexes were determined potentiometrically in 40 mass/mass% ethanol-water mixture containing 0.1 M KCl. The stabilities of the complexes follow the order: Cu²⁺>Ni²⁺>Co²⁺>Mn²⁺. The dissociation constant (pK^H) of MHT and the stability constants (logK) of its metal complexes were determined at different temperatures and the corresponding thermodynamic parameters were calculated and discussed. The proton dissociation process is non-spontaneous, endothermic and entropically unfavoured. The formation of the metal complexes was found to be spontaneous, endothermic and entropically favoured.     

Elucidation of activity of copper and copper oxide nanomaterials for electrocatalytic and photoelectrochemical reduction of carbon dioxide

Copper- and copper oxide–based materials are, in principle, promising components (supports, reactive sites, and visible light–absorbing semiconductors) of electrocatalysts and photocathodes for reduction of carbon dioxide. Electrochemical and photoelectrochemical approaches are generally suitable for the low-temperature CO₂-conversion to carbon-based simple organic fuels or utility chemicals.Different concepts of utilization, including nanostructuring, doping, admixing, preconditioning, modification, or functionalization of various copper- and copper oxide–based systems for catalytic electroreduction and photoelectrochemical reduction of CO₂ are elucidated, as well as important strategies to enhance the systems' overall activity and stability are discussed.     

Synthesis and Structure of 1- and 2-Isomers of (Trimethoxysilylmethyl) and (Silatranylmethyl)benzotriazole

We have synthesized 1- and 2-(trimethylsilylmethyl)- and 1- and 2-(trimethoxysilylmethyl)benzotriazoles by reaction of 1,2,3-benzotriazolylsodium with trimethyl- or trimethoxy(chloromethyl)silane. We obtained 1- and 2-(silatranylmethyl)benzotriazoles by transesterification of the latter with triethanolamine.     

Studies of some monocyclic and bicyclic arylacetonitriles

The high-resolution (1)H, (13)C, (1)H-(1)H COSY and (1)H-(13)C COSY NMR spectra have been recorded in CDCl(3) for arylacetonitriles 1-12 and analyzed. The arylacetonitriles 3-7 exist in two isomeric forms E (methyl group is anti to cyano group) and Z (the methyl group is syn to cyano group) in solution. Normal chair conformation with equatorial orientations of phenyl rings at C-2 and C-6 for monocyclic nitriles 1 and 2, epimeric chair structure EC (axial configuration of methyl group at C-3) for both the E and Z isomers of arylacetonitrile derivatives (3-7) and a distorted boat form, B(3), for the N-acylacetonitrile derivatives (8-10) have been proposed based on NMR data. The bicyclic nitriles 11 and 12 exist in twin chair conformations in solution. DFT calculations and chemical shifts also support these conformations. Geometry optimizations for 1-12 were carried out according to density functional theory using B3LYP/6-31G(d,p) basis set and for 1 and 8 the theoretical geometrical parameters have been compared with those of single crystal measurements.     

Dynamic mechanical and gas transport properties of blends and random copolymers of bisphenol-A polycarbonate and tetramethyl bisphenol-A polycarbonate

Dynamic mechanical and gas transport properties for homogeneous homopolymer blends and random copolymers of bisphenol-A and tetramethyl bisphenol-A polycarbonates (PC-TMPC) were determined. The gas transport measurements were performed at 35°C for the gases He, H₂, O₂, Ar, N₂, CH₄, and CO₂. The results show that the copolymers have lower permeability, apparent diffusion, and solubility coefficients than the blends. Permeability coefficients for blends follow a semilogarithmic ideal mixing rule while copolymers exhibit negative deviations from this. Specific volume measurements show that the free volume available for gas transport is slightly larger in copolymers than in blends of the same composition. These apparently contradictory results may relate to the differences in local mode chain motions observed for the copolymer and blend series. The γ relaxation processes in PC and TMPC seem to operate independently in the blends (no intermolecular coupling) while there is clear evidence for intramolecular coupling in the copolymers. © 1992 John Wiley & Sons, Inc.